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demap_mutation_cancer_type

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The gene AADACL4 has a mutation status of W263_I267del, The gene POU3F1 has a mutation status of G93R, The gene FLG2 has a mutation status of E24K, The gene FCRL5 has a mutation status of L570H, The gene SPTA1 has a mutation status of K601N, The gene DUSP12 has a mutation status of V80A, The gene SGPL1 has a mutation status of W195R, The gene GFRA1 has a mutation status of G24R, The gene TCERG1L has a mutation status of P442S, The gene SYT8 has a mutation status of Q343R, The gene MMP26 has a mutation status of C82F, The gene BBOX1 has a mutation status of W116L, The gene MTA2 has a mutation status of R514W, The gene RELT has a mutation status of G154D, The gene OR8G5 has a mutation status of A119V, The gene PTHLH has a mutation status of P118L, The gene AAAS has a mutation status of E95Ter, The gene PIP4K2C has a mutation status of P7S, The gene F10 has a mutation status of E345K, The gene FANCM has a mutation status of A1042T, The gene ADAM10 has a mutation status of A568T, The gene NEIL1 has a mutation status of R52G, The gene TP53 has a mutation status of R248Q, The gene KRTAP1-1 has a mutation status of R117K, The gene LRRC46 has a mutation status of M244V, The gene CCDC182 has a mutation status of R131P, The gene KCNH6 has a mutation status of V267A, The gene SKOR2 has a mutation status of D146N, The gene MUC16 has a mutation status of V13984M, The gene ZNF257 has a mutation status of C126H, The gene PRR19 has a mutation status of V7I, The gene PPP2R1A has a mutation status of E100K, The gene ZNF600 has a mutation status of L666P, The gene KIR2DL1 has a mutation status of K271N, The gene KLHL29 has a mutation status of D308E, The gene GPR39 has a mutation status of N434I, The gene SP9 has a mutation status of R328S, The gene SGO2 has a mutation status of S125N, The gene UNC80 has a mutation status of H397Y, The gene UNC80 has a mutation status of K2394R, The gene TRIP12 has a mutation status of R1773C, The gene PAX1 has a mutation status of S213L, The gene FAM217B has a mutation status of R156Ter, The gene CPT1B has a mutation status of G668E, The gene CACNA1D has a mutation status of N1535T, The gene CFAP20DC has a mutation status of M676T, The gene CCDC39 has a mutation status of S67L, The gene MUC4 has a mutation status of D2261_T2292del, The gene TLR1 has a mutation status of L302S, The gene PTPN13 has a mutation status of F1296S, The gene RAPGEF2 has a mutation status of E567G, The gene ADAM29 has a mutation status of T800M, The gene PCDH1 has a mutation status of A1047T, The gene MUC22 has a mutation status of T273E, The gene USP42 has a mutation status of L1187V, The gene NOD1 has a mutation status of E172K, The gene VPS41 has a mutation status of K762E, The gene PCLO has a mutation status of T115A, The gene SRI has a mutation status of A9RfsTer44, The gene FZD1 has a mutation status of E149K, The gene ERVW-1 has a mutation status of L333Ter, The gene MUC3A has a mutation status of W18G, The gene COPG2 has a mutation status of I125V, The gene NEFM has a mutation status of E578V, The gene FNTA has a mutation status of K336R, The gene CA1 has a mutation status of H97Y, The gene RUNX1T1 has a mutation status of D457G, The gene AUH has a mutation status of Q314H, The gene ROR2 has a mutation status of V149I, The gene FBP2 has a mutation status of A190V, The gene ZNF618 has a mutation status of A234V, The gene TRIM32 has a mutation status of K627E, The gene CLIC3 has a mutation status of A209T, The gene MT-ND1 has a mutation status of T164A, The gene MT-ND5 has a mutation status of F85L, The gene MT-CYB has a mutation status of T241M, The gene TBL1X has a mutation status of G282D, The gene TASL has a mutation status of S197R, The gene HMGN5 has a mutation status of R4Ter, The gene HMGB3 has a mutation status of T51A, The gene AADACL4 has a mutation status of W263_I267del, The gene GCLM has a mutation status of P244R, The gene FLG2 has a mutation status of E24K, The gene PEAR1 has a mutation status of D1020Y, The gene FCRL5 has a mutation status of L570H, The gene DUSP12 has a mutation status of V80A, The gene GREM2 has a mutation status of V152A, The gene GFRA1 has a mutation status of G24R, The gene SYT8 has a mutation status of Q343R, The gene MMP26 has a mutation status of C82F, The gene BBOX1 has a mutation status of W116L, The gene EIF3M has a mutation status of Q302Ter, The gene MTA2 has a mutation status of R514W, The gene IGHMBP2 has a mutation status of G801S, The gene RELT has a mutation status of G154D, The gene POU2AF1 has a mutation status of L237Ter, The gene OR8G5 has a mutation status of A119V, The gene RHNO1 has a mutation status of I48F, The gene CHD4 has a mutation status of Q1442H, The gene SLC2A14 has a mutation status of E220Ter, The gene PTHLH has a mutation status of P118L, The gene KRT85 has a mutation status of S460T, The gene PIP4K2C has a mutation status of P7S, The gene LRRIQ1 has a mutation status of S1208R, The gene RNFT2 has a mutation status of A93T, The gene F10 has a mutation status of E345K, The gene ADAM10 has a mutation status of A568T, The gene VPS13C has a mutation status of P2297H, The gene NEIL1 has a mutation status of R52G, The gene GTF3C1 has a mutation status of R1089C, The gene AARS1 has a mutation status of M255I, The gene TP53 has a mutation status of R248Q, The gene KRTAP1-1 has a mutation status of R117K, The gene LRRC46 has a mutation status of M244V, The gene KCNH6 has a mutation status of V267A, The gene ABCA9 has a mutation status of W174R, The gene INO80C has a mutation status of A77V, The gene SKOR2 has a mutation status of D146N, The gene MUC16 has a mutation status of V13984M, The gene PRODH2 has a mutation status of P14SfsTer12, The gene ZNF585A has a mutation status of M56L, The gene PRR19 has a mutation status of V7I, The gene PPP2R1A has a mutation status of E100K, The gene ZNF600 has a mutation status of L666P, The gene LILRA2 has a mutation status of W175S, The gene KIR2DL1 has a mutation status of K271N, The gene GEN1 has a mutation status of Q906K, The gene GPR39 has a mutation status of N434I, The gene SP9 has a mutation status of R328S, The gene COL5A2 has a mutation status of P926L, The gene SGO2 has a mutation status of S125N, The gene TRIP12 has a mutation status of R1773C, The gene BMP2 has a mutation status of P187T, The gene PAX1 has a mutation status of S213L, The gene ZNF335 has a mutation status of Q1251H, The gene FAM217B has a mutation status of R156Ter, The gene GART has a mutation status of G377A, The gene CPT1B has a mutation status of G668E, The gene TRANK1 has a mutation status of D1226Y, The gene RBM5 has a mutation status of D660CfsTer67, The gene CACNA1D has a mutation status of N1535T, The gene CFAP20DC has a mutation status of M676T, The gene CCDC39 has a mutation status of S67L, The gene TLR1 has a mutation status of L302S, The gene PTPN13 has a mutation status of F1296S, The gene BLTP1 has a mutation status of R4762C, The gene HSPA4L has a mutation status of N96S, The gene FGF10 has a mutation status of K81E, The gene PCDH1 has a mutation status of A1047T, The gene HLA-DQA2 has a mutation status of A16T, The gene TBC1D32 has a mutation status of I751V, The gene USP42 has a mutation status of L1187V, The gene AHR has a mutation status of K356R, The gene NOD1 has a mutation status of E172K, The gene VPS41 has a mutation status of K762E, The gene CCDC201 has a mutation status of Q122AfsTer53, The gene FZD9 has a mutation status of C111Ter, The gene PCLO has a mutation status of T115A, The gene FZD1 has a mutation status of E149K, The gene KMT2E has a mutation status of L349F, The gene COPG2 has a mutation status of I125V, The gene NEFL has a mutation status of E469D, The gene FNTA has a mutation status of K336R, The gene CA1 has a mutation status of H97Y, The gene RUNX1T1 has a mutation status of D457G, The gene FBP2 has a mutation status of A190V, The gene ECPAS has a mutation status of Q915K, The gene TRIM32 has a mutation status of K627E, The gene COL5A1 has a mutation status of N176K, The gene MT-ND1 has a mutation status of T164A, The gene MT-ND5 has a mutation status of F85L, The gene MT-CYB has a mutation status of T241M, The gene HMGN5 has a mutation status of R4Ter, The gene HMGB3 has a mutation status of T51A	OV
The gene AHDC1 has a mutation status of R72Q, The gene CPT2 has a mutation status of L651S, The gene CYP2J2 has a mutation status of R435S, The gene CELSR2 has a mutation status of R2015K, The gene NRAS has a mutation status of Q61L, The gene MEX3A has a mutation status of H426P, The gene HMCN1 has a mutation status of T5004F, The gene WDFY4 has a mutation status of T885P, The gene PRPF19 has a mutation status of E203L, The gene DHCR7 has a mutation status of G147S, The gene BHLHE41 has a mutation status of A402P, The gene ISCU has a mutation status of M1?, The gene NOS1 has a mutation status of V316A, The gene TMEM132C has a mutation status of L21M, The gene AMER2 has a mutation status of D274A, The gene SEPTIN12 has a mutation status of D356N, The gene SLC5A2 has a mutation status of F535del, The gene IRX5 has a mutation status of Y291S, The gene MLKL has a mutation status of Q413L, The gene ATMIN has a mutation status of E67G, The gene PKD1L2 has a mutation status of T1446K, The gene GALNS has a mutation status of G66V, The gene SPEM2 has a mutation status of R125D, The gene ARL16 has a mutation status of L31R, The gene PHLPP1 has a mutation status of W312G, The gene DIPK1C has a mutation status of L406P, The gene ZNF516 has a mutation status of D486A, The gene GRIN3B has a mutation status of D391G, The gene ABCA7 has a mutation status of H1498P, The gene RANBP3 has a mutation status of V227L, The gene MUC16 has a mutation status of H4357N, The gene VASP has a mutation status of D57A, The gene RASIP1 has a mutation status of D489A, The gene USP29 has a mutation status of A750E, The gene PXDN has a mutation status of C42F, The gene PXDN has a mutation status of R39L, The gene MYT1L has a mutation status of Y110D, The gene GMCL1 has a mutation status of V8G, The gene CSRNP3 has a mutation status of S351N, The gene CCDC150 has a mutation status of Q411H, The gene ABCB6 has a mutation status of E731G, The gene ARMC9 has a mutation status of D90V, The gene TCF15 has a mutation status of R159P, The gene TCF15 has a mutation status of G158P, The gene RASSF2 has a mutation status of I58V, The gene ZNF335 has a mutation status of L1161R, The gene SH3BP1 has a mutation status of Y365Ter, The gene MICALL1 has a mutation status of T313P, The gene IL17RE has a mutation status of I603T, The gene DOCK3 has a mutation status of P1659L, The gene SLC7A14 has a mutation status of V131L, The gene FXR1 has a mutation status of G588C, The gene MUC4 has a mutation status of V2825A, The gene PLEKHG4B has a mutation status of R810C, The gene SLF1 has a mutation status of A620G, The gene FBLL1 has a mutation status of G21I, The gene MAML1 has a mutation status of Q769H, The gene MUC22 has a mutation status of A123S, The gene HLA-DRB5 has a mutation status of D40G, The gene HLA-DRB5 has a mutation status of Q38W, The gene ARMC12 has a mutation status of A22Y, The gene RNF8 has a mutation status of M25G, The gene GTPBP2 has a mutation status of V5G, The gene PTCHD4 has a mutation status of N563S, The gene RWDD1 has a mutation status of Y19S, The gene PPP1R14C has a mutation status of V59G, The gene SLC29A4 has a mutation status of A69T, The gene LMTK2 has a mutation status of Q348K, The gene TMEM130 has a mutation status of E288D, The gene KRBA1 has a mutation status of A316V, The gene TMEM176A has a mutation status of L196F, The gene ATG9B has a mutation status of T96P, The gene SHH has a mutation status of D405G, The gene ADRB3 has a mutation status of D117N, The gene OPRK1 has a mutation status of T144S, The gene TTC39B has a mutation status of K591Q, The gene CDKN2A has a mutation status of R80Ter, The gene CEMIP2 has a mutation status of N914S, The gene GOLM1 has a mutation status of L42V, The gene OR1N2 has a mutation status of L143P, The gene PRRX2 has a mutation status of A194S, The gene CAMSAP1 has a mutation status of L569F, The gene MT-ND4 has a mutation status of F438L, The gene MT-CYB has a mutation status of D171N, The gene MT-CYB has a mutation status of V356M, The gene FAM120C has a mutation status of V138G, The gene PWWP3B has a mutation status of P515S	LAML
The gene PDPN has a mutation status of I142V, The gene RAP1GAP has a mutation status of S629T, The gene SLC44A3 has a mutation status of V448G, The gene SPAG17 has a mutation status of V1266EfsTer4, The gene CD244 has a mutation status of A52L, The gene NAV1 has a mutation status of T1060K, The gene IPO9 has a mutation status of Y363N, The gene INTS7 has a mutation status of L123V, The gene USH2A has a mutation status of Y4318F, The gene CDC42BPA has a mutation status of A19S, The gene OPTN has a mutation status of S269R, The gene DKK1 has a mutation status of M178L, The gene ENTPD1 has a mutation status of H428N, The gene PTPRE has a mutation status of P670S, The gene EPS8L2 has a mutation status of K221Q, The gene DNHD1 has a mutation status of L764W, The gene MADD has a mutation status of S700C, The gene FAM111A has a mutation status of E267Q, The gene TCIRG1 has a mutation status of P390S, The gene MYEOV has a mutation status of C313S, The gene CCDC90B has a mutation status of N171K, The gene EXPH5 has a mutation status of Q1700R, The gene CEP164 has a mutation status of K318Ter, The gene UBE4A has a mutation status of Q39L, The gene ARHGEF12 has a mutation status of D308Y, The gene DERA has a mutation status of G252A, The gene MUC19 has a mutation status of T7365K, The gene MARS1 has a mutation status of L773P, The gene CYP27B1 has a mutation status of I198V, The gene IRAK3 has a mutation status of E494K, The gene CEP83 has a mutation status of C221R, The gene WASHC4 has a mutation status of E4D, The gene TMEM132C has a mutation status of V695L, The gene POLE has a mutation status of I634V, The gene ATP7B has a mutation status of G869E, The gene ZFHX2 has a mutation status of D2061N, The gene CEP170B has a mutation status of L742S, The gene AHNAK2 has a mutation status of N2143D, The gene NPAP1 has a mutation status of D304N, The gene TYRO3 has a mutation status of V233HfsTer11, The gene THAP10 has a mutation status of R132H, The gene STRA6 has a mutation status of S112N, The gene REXO5 has a mutation status of L436FfsTer9, The gene CD19 has a mutation status of L285P, The gene CES3 has a mutation status of F216L, The gene SPEM2 has a mutation status of R126H, The gene TP53 has a mutation status of M133K, The gene KRT39 has a mutation status of L72V, The gene KRT40 has a mutation status of R159T, The gene HOXB7 has a mutation status of G64R, The gene TMEM200C has a mutation status of D528E, The gene CIDEA has a mutation status of E88D, The gene DSG4 has a mutation status of G400EfsTer5, The gene HNRNPM has a mutation status of P331H, The gene ZNF737 has a mutation status of T523S, The gene TBCB has a mutation status of G131S, The gene CAPN12 has a mutation status of R518L, The gene KLK3 has a mutation status of R201L, The gene CNOT3 has a mutation status of E220K, The gene C2orf16 has a mutation status of E4236A, The gene TIA1 has a mutation status of G284AfsTer7, The gene THNSL2 has a mutation status of A10T, The gene SULT1C2 has a mutation status of F126_L127delinsLI, The gene EDAR has a mutation status of G226A, The gene SMPD4 has a mutation status of K365T, The gene OSBPL6 has a mutation status of S912A, The gene TTN has a mutation status of V26715A, The gene PASK has a mutation status of E1305RfsTer4, The gene DNAAF9 has a mutation status of L117SfsTer16, The gene BMP2 has a mutation status of G88A, The gene PAK5 has a mutation status of M338L, The gene PCSK2 has a mutation status of R605W, The gene TTC3 has a mutation status of T357I, The gene ZNRF3 has a mutation status of R4H, The gene CYP2D7 has a mutation status of L486F, The gene TUBGCP6 has a mutation status of N1186S, The gene CHL1 has a mutation status of L427V, The gene RPL32 has a mutation status of A3S, The gene DALRD3 has a mutation status of V524A, The gene NISCH has a mutation status of E663K, The gene CLDND1 has a mutation status of R80W, The gene SENP7 has a mutation status of M511V, The gene BOC has a mutation status of N349D, The gene HGD has a mutation status of E27A, The gene PRR20G has a mutation status of P42T, The gene ESYT3 has a mutation status of E4Q, The gene EIF2A has a mutation status of H491R, The gene IGSF10 has a mutation status of S1873N, The gene TP63 has a mutation status of E636Q, The gene OPA1 has a mutation status of I24T, The gene MUC4 has a mutation status of F4515N, The gene FGFR3 has a mutation status of M431V, The gene OTOP1 has a mutation status of M495L, The gene MAN2B2 has a mutation status of N260S, The gene CORIN has a mutation status of S683R, The gene SPEF2 has a mutation status of L5R, The gene VCAN has a mutation status of V955D, The gene FBXL17 has a mutation status of C20S, The gene PCDHB4 has a mutation status of V662E, The gene SLC36A3 has a mutation status of A158V, The gene ADAM19 has a mutation status of P315R, The gene GABRP has a mutation status of Q409P, The gene MRS2 has a mutation status of G397A, The gene H2AC7 has a mutation status of P81L, The gene MAP3K7 has a mutation status of S328T, The gene MAP3K5 has a mutation status of T1308I, The gene SYNJ2 has a mutation status of T1390A, The gene FOXK1 has a mutation status of A33D, The gene CDHR3 has a mutation status of T631P, The gene KCP has a mutation status of W1224C, The gene UNC5D has a mutation status of S226A, The gene RPL7 has a mutation status of N80Y, The gene JPH1 has a mutation status of G215V, The gene VPS13B has a mutation status of Y1164H, The gene EXOSC4 has a mutation status of E238Q, The gene ZNF251 has a mutation status of T456A, The gene JAK2 has a mutation status of V617F, The gene TRIM14 has a mutation status of G113E, The gene ENG has a mutation status of H108Y, The gene MT-ND5 has a mutation status of T533A, The gene MT-CYB has a mutation status of T158A, The gene ZXDA has a mutation status of Q138L, The gene PDPN has a mutation status of I142V, The gene CASP9 has a mutation status of G402A, The gene RAP1GAP has a mutation status of S629T, The gene SLC44A3 has a mutation status of V448G, The gene SPAG17 has a mutation status of V1266EfsTer4, The gene CD244 has a mutation status of A52L, The gene NAV1 has a mutation status of T1060K, The gene IPO9 has a mutation status of Y363N, The gene INTS7 has a mutation status of L123V, The gene USH2A has a mutation status of Y4318F, The gene DEGS1 has a mutation status of P266T, The gene CDC42BPA has a mutation status of A19S, The gene OPTN has a mutation status of S269R, The gene DKK1 has a mutation status of M178L, The gene ENTPD1 has a mutation status of H428N, The gene PTPRE has a mutation status of P670S, The gene EPS8L2 has a mutation status of K221Q, The gene DNHD1 has a mutation status of L764W, The gene MADD has a mutation status of S700C, The gene FAM111A has a mutation status of E267Q, The gene TCIRG1 has a mutation status of P390S, The gene MYEOV has a mutation status of C313S, The gene CCDC90B has a mutation status of N171K, The gene EXPH5 has a mutation status of Q1700R, The gene CEP164 has a mutation status of K318Ter, The gene UBE4A has a mutation status of Q39L, The gene ARHGEF12 has a mutation status of D308Y, The gene DERA has a mutation status of G252A, The gene MUC19 has a mutation status of S6579D, The gene MUC19 has a mutation status of T7365K, The gene MARS1 has a mutation status of L773P, The gene CYP27B1 has a mutation status of I198V, The gene IRAK3 has a mutation status of E494K, The gene CEP83 has a mutation status of C221R, The gene WASHC4 has a mutation status of E4D, The gene TMEM132C has a mutation status of V695L, The gene POLE has a mutation status of I634V, The gene ATP7B has a mutation status of G869E, The gene ZFHX2 has a mutation status of D2061N, The gene CEP170B has a mutation status of L742S, The gene NPAP1 has a mutation status of D304N, The gene TMEM87A has a mutation status of F426EfsTer2, The gene TMEM87A has a mutation status of M424VfsTer51, The gene THAP10 has a mutation status of R132H, The gene STRA6 has a mutation status of S112N, The gene REXO5 has a mutation status of L436FfsTer9, The gene CD19 has a mutation status of L285P, The gene CES3 has a mutation status of F216L, The gene SPEM2 has a mutation status of R126H, The gene TP53 has a mutation status of M133K, The gene KRT39 has a mutation status of L72V, The gene KRTAP9-6 has a mutation status of G106C, The gene HOXB7 has a mutation status of G64R, The gene TMEM200C has a mutation status of D528E, The gene CIDEA has a mutation status of E88D, The gene DSG4 has a mutation status of G400EfsTer5, The gene HNRNPM has a mutation status of P331H, The gene MUC16 has a mutation status of Q13253E, The gene MUC16 has a mutation status of H12873R, The gene ZNF737 has a mutation status of T523S, The gene TBCB has a mutation status of G131S, The gene CAPN12 has a mutation status of R518L, The gene KLK3 has a mutation status of R201L, The gene CNOT3 has a mutation status of E220K, The gene C2orf16 has a mutation status of E4236A, The gene TIA1 has a mutation status of G284AfsTer7, The gene THNSL2 has a mutation status of A10T, The gene SULT1C2 has a mutation status of F126_L127delinsLI, The gene EDAR has a mutation status of G226A, The gene SMPD4 has a mutation status of K365T, The gene OSBPL6 has a mutation status of S912A, The gene TTN has a mutation status of V26715A, The gene PASK has a mutation status of E1305RfsTer4, The gene DNAAF9 has a mutation status of L117SfsTer16, The gene BMP2 has a mutation status of G88A, The gene PAK5 has a mutation status of M338L, The gene PCSK2 has a mutation status of R605W, The gene TTC3 has a mutation status of T357I, The gene CYP2D7 has a mutation status of L486F, The gene TUBGCP6 has a mutation status of N1186S, The gene CHL1 has a mutation status of L427V, The gene RPL32 has a mutation status of A3S, The gene DALRD3 has a mutation status of V524A, The gene NISCH has a mutation status of E663K, The gene CLDND1 has a mutation status of R80W, The gene SENP7 has a mutation status of M511V, The gene BOC has a mutation status of N349D, The gene HGD has a mutation status of E27A, The gene ESYT3 has a mutation status of E4Q, The gene EIF2A has a mutation status of H491R, The gene IGSF10 has a mutation status of S1873N, The gene TP63 has a mutation status of E636Q, The gene OPA1 has a mutation status of I24T, The gene MUC4 has a mutation status of F4515N, The gene MUC4 has a mutation status of S2661_T2708del, The gene FGFR3 has a mutation status of M431V, The gene OTOP1 has a mutation status of M495L, The gene MAN2B2 has a mutation status of N260S, The gene CORIN has a mutation status of S683R, The gene SPEF2 has a mutation status of L5R, The gene VCAN has a mutation status of V955D, The gene FBXL17 has a mutation status of C20S, The gene PCDHB4 has a mutation status of V662E, The gene SLC36A3 has a mutation status of A158V, The gene ADAM19 has a mutation status of P315R, The gene GABRP has a mutation status of Q409P, The gene MRS2 has a mutation status of G397A, The gene H2AC7 has a mutation status of P81L, The gene MUC22 has a mutation status of G1102AfsTer30, The gene MAP3K7 has a mutation status of S328T, The gene MAP3K5 has a mutation status of T1308I, The gene SYNJ2 has a mutation status of T1390A, The gene ZNF727 has a mutation status of K275E, The gene MUC3A has a mutation status of W18G, The gene CDHR3 has a mutation status of T631P, The gene KCP has a mutation status of W1224C, The gene UNC5D has a mutation status of S226A, The gene RPL7 has a mutation status of N80Y, The gene JPH1 has a mutation status of G215V, The gene VPS13B has a mutation status of Y1164H, The gene EXOSC4 has a mutation status of E238Q, The gene ZNF251 has a mutation status of T456A, The gene JAK2 has a mutation status of V617F, The gene TRIM14 has a mutation status of G113E, The gene ENG has a mutation status of H108Y, The gene MT-ND5 has a mutation status of T533A, The gene MT-CYB has a mutation status of T158A	LAML
The gene MACF1 has a mutation status of A6595T, The gene CTBS has a mutation status of A117GfsTer2, The gene ARHGAP29 has a mutation status of L878R, The gene USH2A has a mutation status of K1986R, The gene ZNF695 has a mutation status of A360T, The gene OR1C1 has a mutation status of A67S, The gene LIPJ has a mutation status of Y295H, The gene ACSM6 has a mutation status of Q340H, The gene JAKMIP3 has a mutation status of A556V, The gene OR5D14 has a mutation status of I53S, The gene DDB1 has a mutation status of V364M, The gene DHCR7 has a mutation status of V402G, The gene ZW10 has a mutation status of R76K, The gene HVCN1 has a mutation status of M91T, The gene FLT3 has a mutation status of V592A, The gene WDFY2 has a mutation status of D285GfsTer7, The gene IRS2 has a mutation status of R930PfsTer61, The gene NDRG2 has a mutation status of Q8Ter, The gene SALL2 has a mutation status of P44R, The gene TRAV12-3 has a mutation status of Q28HfsTer38, The gene ATP6V1D has a mutation status of E110K, The gene ACOT6 has a mutation status of V94G, The gene PPP4R4 has a mutation status of G71E, The gene AHNAK2 has a mutation status of V2471L, The gene UMOD has a mutation status of S291G, The gene ATXN2L has a mutation status of P41S, The gene ZNF747 has a mutation status of R299P, The gene NECAB2 has a mutation status of T212P, The gene MBTPS1 has a mutation status of V814I, The gene TP53 has a mutation status of R273H, The gene NLK has a mutation status of S257Ter, The gene ARHGAP23 has a mutation status of V1409G, The gene XYLT2 has a mutation status of F520L, The gene SEPTIN9 has a mutation status of Q118P, The gene TNRC6C has a mutation status of A191D, The gene DSG1 has a mutation status of E708K, The gene HCN2 has a mutation status of A141L, The gene CAMSAP3 has a mutation status of M600T, The gene CHST8 has a mutation status of D67N, The gene RYR1 has a mutation status of S1489N, The gene EXOC3L2 has a mutation status of Q84K, The gene LILRA2 has a mutation status of W175S, The gene TDRD15 has a mutation status of G1784A, The gene PPP4R3B has a mutation status of P253R, The gene ADD2 has a mutation status of E301G, The gene CD207 has a mutation status of H229Q, The gene NCKAP5 has a mutation status of P1829L, The gene FSIP2 has a mutation status of T4430S, The gene SCYGR2 has a mutation status of C31R, The gene ALPI has a mutation status of M229L, The gene USP40 has a mutation status of H666L, The gene PASK has a mutation status of V178L, The gene VPS16 has a mutation status of T323N, The gene ASXL1 has a mutation status of L1393RfsTer30, The gene GGT7 has a mutation status of L331F, The gene RALGAPB has a mutation status of P914S, The gene L3MBTL1 has a mutation status of V134G, The gene STAU1 has a mutation status of M82V, The gene RUNX1 has a mutation status of A134V, The gene CABIN1 has a mutation status of D977G, The gene PNPLA5 has a mutation status of G288R, The gene TTC14 has a mutation status of F265L, The gene MED28 has a mutation status of T68A, The gene ARAP2 has a mutation status of T628NfsTer22, The gene TLR10 has a mutation status of D362N, The gene CENPE has a mutation status of S859L, The gene CFI has a mutation status of C266R, The gene FAT4 has a mutation status of Y4219Ter, The gene SH3RF1 has a mutation status of Q566K, The gene DNAH5 has a mutation status of E2558D, The gene MAP3K1 has a mutation status of V936L, The gene ADGRV1 has a mutation status of A4147P, The gene LECT2 has a mutation status of Y81S, The gene SGCD has a mutation status of E262K, The gene HLA-C has a mutation status of S140L, The gene HLA-B has a mutation status of Y140L, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB1 has a mutation status of P84E, The gene ITPR3 has a mutation status of L1811R, The gene AARS2 has a mutation status of S71R, The gene ADGRF1 has a mutation status of T564I, The gene FAM184A has a mutation status of V227A, The gene FAM220A has a mutation status of T138S, The gene PKD1L1 has a mutation status of F1588I, The gene ASB4 has a mutation status of R318Q, The gene ST7 has a mutation status of A378S, The gene KIF13B has a mutation status of K1749E, The gene TCEA1 has a mutation status of S128Ter, The gene TGS1 has a mutation status of E330G, The gene HNF4G has a mutation status of S189A, The gene KANK1 has a mutation status of K1179N, The gene PCSK5 has a mutation status of S87R, The gene SHC3 has a mutation status of N568_H569insRHLIN, The gene OLFML2A has a mutation status of S57R, The gene NDOR1 has a mutation status of K504E, The gene ARMCX4 has a mutation status of G1300C, The gene L1CAM has a mutation status of Q361K, The gene CTBS has a mutation status of A117GfsTer2, The gene KCNN3 has a mutation status of L66Q, The gene USH2A has a mutation status of K1986R, The gene ZNF695 has a mutation status of A360T, The gene LIPJ has a mutation status of Y295H, The gene JAKMIP3 has a mutation status of A556V, The gene OR4A16 has a mutation status of K22Q, The gene OR4A16 has a mutation status of N132T, The gene OR4A16 has a mutation status of I319A, The gene DDB1 has a mutation status of V364M, The gene ZW10 has a mutation status of R76K, The gene KCNA5 has a mutation status of V407L, The gene IRAG2 has a mutation status of A714S, The gene MUC19 has a mutation status of R4223_D4252delextTer?, The gene HVCN1 has a mutation status of M91T, The gene FLT3 has a mutation status of V592A, The gene NDRG2 has a mutation status of Q8Ter, The gene SALL2 has a mutation status of P44R, The gene TRAV12-3 has a mutation status of Q28HfsTer38, The gene ATP6V1D has a mutation status of E110K, The gene PPP4R4 has a mutation status of G71E, The gene AHNAK2 has a mutation status of V2471L, The gene UMOD has a mutation status of S291G, The gene ATXN2L has a mutation status of P41S, The gene ZNF747 has a mutation status of R299P, The gene MBTPS1 has a mutation status of V814I, The gene TP53 has a mutation status of R273H, The gene ALOX12B has a mutation status of S439N, The gene TEKT3 has a mutation status of I153Ter, The gene NLK has a mutation status of S257Ter, The gene KRTAP4-7 has a mutation status of P117R, The gene XYLT2 has a mutation status of F520L, The gene SEPTIN9 has a mutation status of Q118P, The gene TNRC6C has a mutation status of A191D, The gene CHST8 has a mutation status of D67N, The gene RYR1 has a mutation status of S1489N, The gene TRIM28 has a mutation status of P429L, The gene TDRD15 has a mutation status of G1784A, The gene PPP4R3B has a mutation status of P253R, The gene ADD2 has a mutation status of E301G, The gene CD207 has a mutation status of H229Q, The gene NCKAP5 has a mutation status of P1829L, The gene COBLL1 has a mutation status of R856Q, The gene FSIP2 has a mutation status of C3645R, The gene ALPI has a mutation status of M229L, The gene USP40 has a mutation status of H666L, The gene PASK has a mutation status of V178L, The gene VPS16 has a mutation status of T323N, The gene ASXL1 has a mutation status of L1393RfsTer30, The gene GGT7 has a mutation status of L331F, The gene RALGAPB has a mutation status of P914S, The gene RUNX1 has a mutation status of A134V, The gene U2AF1 has a mutation status of Q157P, The gene CABIN1 has a mutation status of D977G, The gene PNPLA5 has a mutation status of G288R, The gene RFT1 has a mutation status of P461S, The gene TTC14 has a mutation status of F265L, The gene MUC4 has a mutation status of T3942L, The gene MUC4 has a mutation status of L3542T, The gene MUC4 has a mutation status of S3541D, The gene MUC4 has a mutation status of T1684_G1685insSTSSASTGHATPLPVTDNSSVSTGHATPLPVT, The gene FBXL5 has a mutation status of E104Ter, The gene MED28 has a mutation status of T68A, The gene ARAP2 has a mutation status of T628NfsTer22, The gene TLR10 has a mutation status of D362N, The gene CENPE has a mutation status of S859L, The gene CFI has a mutation status of C266R, The gene SH3RF1 has a mutation status of Q566K, The gene MAP3K1 has a mutation status of V936L, The gene ADGRV1 has a mutation status of A4147P, The gene LECT2 has a mutation status of Y81S, The gene ADGRF1 has a mutation status of T564I, The gene FAM184A has a mutation status of V227A, The gene FAM220A has a mutation status of T138S, The gene PKD1L1 has a mutation status of F1588I, The gene ERVW-1 has a mutation status of L333Ter, The gene ASB4 has a mutation status of R318Q, The gene ST7 has a mutation status of A378S, The gene TCEA1 has a mutation status of S128Ter, The gene TGS1 has a mutation status of E330G, The gene HNF4G has a mutation status of S189A, The gene KANK1 has a mutation status of K1179N, The gene OLFML2A has a mutation status of S57R, The gene NDOR1 has a mutation status of K504E, The gene MT-ND4 has a mutation status of A226T, The gene PWWP3B has a mutation status of S324T	LAML
The gene FBXO44 has a mutation status of E59K, The gene KLHDC7A has a mutation status of V544M, The gene FNDC5 has a mutation status of P34L, The gene EPS15 has a mutation status of T461K, The gene USP1 has a mutation status of Q332E, The gene ROR1 has a mutation status of G358D, The gene PDE4B has a mutation status of S128N, The gene IL23R has a mutation status of V338A, The gene MSH4 has a mutation status of A802V, The gene AP4B1 has a mutation status of F405SfsTer53, The gene MRPL9 has a mutation status of R72L, The gene UFC1 has a mutation status of L142V, The gene GORAB has a mutation status of Q37Ter, The gene FMO4 has a mutation status of G196R, The gene CACNA1E has a mutation status of M791I, The gene SHCBP1L has a mutation status of A75T, The gene ARPC5 has a mutation status of A75E, The gene HMCN1 has a mutation status of S580G, The gene TPR has a mutation status of S1824G, The gene IRF6 has a mutation status of G170S, The gene KCNK2 has a mutation status of T64M, The gene USH2A has a mutation status of R4092I, The gene BPNT1 has a mutation status of I254V, The gene NUP133 has a mutation status of L935H, The gene SPRTN has a mutation status of I422YfsTer11, The gene RYR2 has a mutation status of A2346E, The gene RBP3 has a mutation status of H633Y, The gene CDH23 has a mutation status of R2304W, The gene HECTD2 has a mutation status of L156I, The gene PPRC1 has a mutation status of T844N, The gene ATRNL1 has a mutation status of T1362A, The gene CDHR5 has a mutation status of A607_E637del, The gene PAX6 has a mutation status of S110F, The gene PTPMT1 has a mutation status of V143M, The gene OR8H3 has a mutation status of L130V, The gene LBHD1 has a mutation status of V167M, The gene SIK3 has a mutation status of P409Q, The gene OR4D5 has a mutation status of G95D, The gene GLB1L3 has a mutation status of G91R, The gene PRB3 has a mutation status of R242SfsTer14, The gene KRAS has a mutation status of G12D, The gene IPO8 has a mutation status of E367Q, The gene PKP2 has a mutation status of E478K, The gene PKP2 has a mutation status of S172T, The gene ZCRB1 has a mutation status of E153Q, The gene TMTC2 has a mutation status of H126P, The gene TMEM132C has a mutation status of S19I, The gene KBTBD7 has a mutation status of V287M, The gene WDFY2 has a mutation status of E94Ter, The gene SUGT1 has a mutation status of F18C, The gene PCDH17 has a mutation status of G393R, The gene CHAMP1 has a mutation status of H756Y, The gene OR4K17 has a mutation status of Ter313YextTer13, The gene ZNF410 has a mutation status of G450R, The gene NRXN3 has a mutation status of L1100I, The gene SERPINA4 has a mutation status of D116N, The gene IGHV4-59 has a mutation status of E35Q, The gene GOLGA6L2 has a mutation status of R427L, The gene GABRA5 has a mutation status of L24V, The gene FMN1 has a mutation status of S272A, The gene MGA has a mutation status of S276I, The gene FEM1B has a mutation status of N56S, The gene TLNRD1 has a mutation status of A310V, The gene ADAMTSL3 has a mutation status of T1412N, The gene CRAMP1 has a mutation status of R53L, The gene SRRM2 has a mutation status of S421I, The gene AARS1 has a mutation status of R333P, The gene BANP has a mutation status of R67W, The gene SPIRE2 has a mutation status of R505W, The gene TRPV3 has a mutation status of A269E, The gene CHRNE has a mutation status of P333VfsTer53, The gene POLR2A has a mutation status of T1118M, The gene POLR2A has a mutation status of A1205S, The gene ALOX15B has a mutation status of S334I, The gene SOX9 has a mutation status of R120L, The gene KCTD2 has a mutation status of Q53L, The gene UBE2O has a mutation status of E723A, The gene MBP has a mutation status of K138R, The gene SALL3 has a mutation status of R239W, The gene C3 has a mutation status of Q417K, The gene TRAPPC5 has a mutation status of I146N, The gene OR2Z1 has a mutation status of C241Ter, The gene OR7G2 has a mutation status of I260M, The gene YIPF2 has a mutation status of G107AfsTer35, The gene SMARCA4 has a mutation status of R973W, The gene NOTCH3 has a mutation status of S2096L, The gene ABHD8 has a mutation status of S423E, The gene ZNF486 has a mutation status of P349A, The gene ZNF43 has a mutation status of E479Ter, The gene TSHZ3 has a mutation status of A736S, The gene ZNF790 has a mutation status of H461R, The gene GYS1 has a mutation status of T75GfsTer88, The gene ZNF845 has a mutation status of G949C, The gene KIR2DL1 has a mutation status of D184N, The gene NLRP5 has a mutation status of L72_K74del, The gene ZNF805 has a mutation status of T244K, The gene ZSCAN18 has a mutation status of E213K, The gene CPSF3 has a mutation status of L605S, The gene WDR35 has a mutation status of L925HfsTer15, The gene APOB has a mutation status of E2740Ter, The gene BCL11A has a mutation status of E91Ter, The gene RANBP2 has a mutation status of D2673G, The gene ARHGEF4 has a mutation status of A816D, The gene FIGN has a mutation status of F18L, The gene HNRNPA3 has a mutation status of Y323C, The gene TTN has a mutation status of A35263F, The gene TTN has a mutation status of L19644I, The gene TTN has a mutation status of S9616Y, The gene ZNF804A has a mutation status of W725C, The gene BMPR2 has a mutation status of R491Q, The gene ABCA12 has a mutation status of Y643Ter, The gene ASB18 has a mutation status of A144T, The gene COL6A3 has a mutation status of V2778M, The gene HDAC4 has a mutation status of Q125E, The gene NINL has a mutation status of G232Ter, The gene PPP1R16B has a mutation status of C302Y, The gene ZMYND8 has a mutation status of E585D, The gene TAF4 has a mutation status of A143S, The gene MYT1 has a mutation status of A709T, The gene CHODL has a mutation status of S6L, The gene MRAP has a mutation status of V26G, The gene PDGFB has a mutation status of R3L, The gene NEK10 has a mutation status of L991F, The gene SUSD5 has a mutation status of G573S, The gene CTNNB1 has a mutation status of M14_E15insINYQDDAELATRAIP, The gene ZBTB47 has a mutation status of R403_P404delinsT, The gene BSN has a mutation status of T3581M, The gene MST1 has a mutation status of V598A, The gene SFMBT1 has a mutation status of H344Y, The gene ZNF717 has a mutation status of V22A, The gene TBC1D23 has a mutation status of K647Q, The gene RASA2 has a mutation status of Y194Ter, The gene MECOM has a mutation status of T596I, The gene FAM43A has a mutation status of Y70C, The gene ACAP2 has a mutation status of A363D, The gene MUC4 has a mutation status of T3942L, The gene NRROS has a mutation status of A127S, The gene ZFYVE28 has a mutation status of E818Ter, The gene HTT has a mutation status of Q1621H, The gene ADRA2C has a mutation status of R166C, The gene TRMT44 has a mutation status of R629S, The gene SLIT2 has a mutation status of C436F, The gene NWD2 has a mutation status of F775L, The gene SLC4A4 has a mutation status of D1060N, The gene SEC31A has a mutation status of E583V, The gene MEPE has a mutation status of D412Y, The gene ENPEP has a mutation status of W868L, The gene ZGRF1 has a mutation status of K1690N, The gene PCDH10 has a mutation status of A351S, The gene FHIP1A has a mutation status of S94A, The gene CPE has a mutation status of A266V, The gene ADAMTS16 has a mutation status of K901R, The gene DNAH5 has a mutation status of V1672M, The gene PRDM9 has a mutation status of D787Y, The gene PDZD2 has a mutation status of Q777P, The gene CWC27 has a mutation status of A351S, The gene ADAMTS6 has a mutation status of D351N, The gene MAST4 has a mutation status of D1166G, The gene ADGRV1 has a mutation status of G3138C, The gene PCDHGA10 has a mutation status of A335V, The gene FOXF2 has a mutation status of S49L, The gene ERVFRD-1 has a mutation status of G366D, The gene SYNGAP1 has a mutation status of S52L, The gene EYS has a mutation status of Y563C, The gene EYS has a mutation status of G484V, The gene ADGRB3 has a mutation status of D854Y, The gene CASP8AP2 has a mutation status of V189I, The gene PTPRK has a mutation status of L561V, The gene SLC18B1 has a mutation status of N218H, The gene USP42 has a mutation status of P857R, The gene USP42 has a mutation status of H1083_E1104del, The gene SFRP4 has a mutation status of S122G, The gene AMPH has a mutation status of L191V, The gene POU6F2 has a mutation status of H311N, The gene HECW1 has a mutation status of E586K, The gene ABCA13 has a mutation status of L4668R, The gene SEPTIN14 has a mutation status of F356V, The gene TYW1 has a mutation status of I662LfsTer75, The gene PTPN12 has a mutation status of K141R, The gene ZAN has a mutation status of T2778Ter, The gene MUC3A has a mutation status of T303V, The gene FOXP2 has a mutation status of S442R, The gene BRAF has a mutation status of E204L, The gene CLCN1 has a mutation status of D19G, The gene SHH has a mutation status of G221R, The gene ENTPD4 has a mutation status of Y105Ter, The gene PREX2 has a mutation status of Q898H, The gene GRINA has a mutation status of A257V, The gene SMC5 has a mutation status of Y560H, The gene TGFBR1 has a mutation status of D333H, The gene TGFBR1 has a mutation status of R413Ter, The gene TRIM32 has a mutation status of A585V, The gene OLFM1 has a mutation status of S48R, The gene MT-ND5 has a mutation status of T533M, The gene RPS6KA6 has a mutation status of R310S, The gene DCX has a mutation status of K112N, The gene SLITRK2 has a mutation status of C220F	COAD
The gene PUM1 has a mutation status of L942F, The gene TEKT2 has a mutation status of D332E, The gene PLPPR5 has a mutation status of R299Ter, The gene COL11A1 has a mutation status of E335Ter, The gene CELSR2 has a mutation status of R2015K, The gene FLG2 has a mutation status of Y350H, The gene USF1 has a mutation status of V140I, The gene CD46 has a mutation status of W216Ter, The gene ANGEL2 has a mutation status of V16M, The gene FMN2 has a mutation status of P971S, The gene BECN2 has a mutation status of R311Ter, The gene ZEB1 has a mutation status of M1094I, The gene OR51B5 has a mutation status of E109K, The gene USH1C has a mutation status of S267F, The gene ANO3 has a mutation status of D111N, The gene BBOX1 has a mutation status of T255I, The gene OR8J3 has a mutation status of S110L, The gene SLC22A25 has a mutation status of R277K, The gene NECTIN1 has a mutation status of E98K, The gene SORL1 has a mutation status of D1405N, The gene OR8D2 has a mutation status of I282F, The gene NCAPD2 has a mutation status of G667E, The gene CLEC12A has a mutation status of R40L, The gene MUC19 has a mutation status of S780F, The gene MUC19 has a mutation status of N4824T, The gene NELL2 has a mutation status of H235Y, The gene MON2 has a mutation status of P258S, The gene OTOGL has a mutation status of E1902K, The gene LIN7A has a mutation status of A206S, The gene MGAT4C has a mutation status of D327N, The gene HIP1R has a mutation status of A327RfsTer9, The gene ATP8A2 has a mutation status of I126N, The gene LRRC63 has a mutation status of P159L, The gene CIPC has a mutation status of T380I, The gene MAP1A has a mutation status of E860Q, The gene GTF2A2 has a mutation status of V90M, The gene WDR93 has a mutation status of P257L, The gene LRRC36 has a mutation status of S467L, The gene WWOX has a mutation status of D58H, The gene ANKRD11 has a mutation status of I433R, The gene SPEM2 has a mutation status of H131R, The gene BLTP2 has a mutation status of G1531E, The gene MMP28 has a mutation status of P453S, The gene HSF5 has a mutation status of T75S, The gene INTS2 has a mutation status of E191SfsTer2, The gene ABCA8 has a mutation status of M62I, The gene ENDOV has a mutation status of P235L, The gene ASPSCR1 has a mutation status of E331V, The gene PTPRM has a mutation status of Q885E, The gene ANKRD12 has a mutation status of L1009S, The gene ANKRD12 has a mutation status of D1013Y, The gene GAREM1 has a mutation status of S780F, The gene SETBP1 has a mutation status of P558L, The gene ONECUT2 has a mutation status of E216K, The gene USHBP1 has a mutation status of G467E, The gene ZNF723 has a mutation status of C371S, The gene PROSER3 has a mutation status of P534S, The gene FGF21 has a mutation status of S191P, The gene CGB7 has a mutation status of C54W, The gene KLK7 has a mutation status of K197N, The gene ZNF415 has a mutation status of L511C, The gene CAPN14 has a mutation status of W586G, The gene ZAP70 has a mutation status of V470F, The gene SULT1C4 has a mutation status of H299Y, The gene CYTIP has a mutation status of I42S, The gene SCN3A has a mutation status of S665L, The gene SCN1A has a mutation status of R568Q, The gene XIRP2 has a mutation status of S2471R, The gene TTN has a mutation status of L23972PfsTer15, The gene TTN has a mutation status of W8784Ter, The gene ZNF804A has a mutation status of P1193S, The gene HECW2 has a mutation status of G216E, The gene FN1 has a mutation status of I1739S, The gene SCYGR2 has a mutation status of H97S, The gene INPP5D has a mutation status of H753Y, The gene BPIFB3 has a mutation status of H426R, The gene EPB41L1 has a mutation status of G549S, The gene MYL9 has a mutation status of I49T, The gene CDH22 has a mutation status of P497del, The gene CDH22 has a mutation status of N493IfsTer88, The gene CECR2 has a mutation status of S436F, The gene CNOT10 has a mutation status of G694S, The gene DNAH12 has a mutation status of L1060S, The gene STXBP5L has a mutation status of G299E, The gene CHRD has a mutation status of E500K, The gene ATP13A5 has a mutation status of W57Ter, The gene MUC4 has a mutation status of L3542T, The gene MUC4 has a mutation status of S3541D, The gene MUC4 has a mutation status of A998T, The gene DGKQ has a mutation status of C218H, The gene CCDC158 has a mutation status of E206K, The gene ADH1A has a mutation status of S342L, The gene TLL1 has a mutation status of S932F, The gene FBXO8 has a mutation status of R219C, The gene MYO10 has a mutation status of L1851SfsTer25, The gene NIPBL has a mutation status of T2731S, The gene NUP155 has a mutation status of E536Ter, The gene DDX4 has a mutation status of P165S, The gene MAST4 has a mutation status of E2456K, The gene PCDHB13 has a mutation status of L726F, The gene TCERG1 has a mutation status of A179S, The gene RIPK1 has a mutation status of A569V, The gene H2BC12 has a mutation status of T53A, The gene HLA-DQB1 has a mutation status of P84E, The gene HLA-DQB2 has a mutation status of V37Y, The gene ADGRF5 has a mutation status of P413L, The gene PHIP has a mutation status of T667I, The gene BCKDHB has a mutation status of Q267Ter, The gene NPSR1 has a mutation status of V124I, The gene ABCA13 has a mutation status of I3759N, The gene MUC3A has a mutation status of N2136_E2152del, The gene MUC3A has a mutation status of P2711S, The gene KIAA1549 has a mutation status of K615E, The gene BRAF has a mutation status of V600E, The gene KRBA1 has a mutation status of D119N, The gene GIMAP8 has a mutation status of S21L, The gene RAD21 has a mutation status of L229S, The gene ZFTRAF1 has a mutation status of G45D, The gene MPDZ has a mutation status of E702M, The gene PRSS3 has a mutation status of D102I, The gene UNC13B has a mutation status of E437AfsTer3, The gene UNC13B has a mutation status of P2950S, The gene SIT1 has a mutation status of V84G, The gene OR13C2 has a mutation status of H20P, The gene ECPAS has a mutation status of R1265Ter, The gene MED12 has a mutation status of E33K, The gene SERPINA7 has a mutation status of P383L, The gene SLITRK4 has a mutation status of G515W, The gene PUM1 has a mutation status of L942F, The gene PLPPR5 has a mutation status of R299Ter, The gene CELSR2 has a mutation status of R2015K, The gene FLG2 has a mutation status of Y350H, The gene USF1 has a mutation status of V140I, The gene CD46 has a mutation status of W216Ter, The gene ANGEL2 has a mutation status of V16M, The gene FMN2 has a mutation status of P971S, The gene BECN2 has a mutation status of R311Ter, The gene ZEB1 has a mutation status of M1094I, The gene OR51B5 has a mutation status of E109K, The gene USH1C has a mutation status of S267F, The gene ANO3 has a mutation status of D111N, The gene BBOX1 has a mutation status of T255I, The gene OR8J3 has a mutation status of S110L, The gene SLC22A25 has a mutation status of R277K, The gene NECTIN1 has a mutation status of E98K, The gene SORL1 has a mutation status of D1405N, The gene OR8D2 has a mutation status of I282F, The gene NCAPD2 has a mutation status of G667E, The gene CLEC12A has a mutation status of R40L, The gene MUC19 has a mutation status of S780F, The gene NELL2 has a mutation status of H235Y, The gene MON2 has a mutation status of P258S, The gene OTOGL has a mutation status of E1902K, The gene MGAT4C has a mutation status of D327N, The gene HIP1R has a mutation status of A327RfsTer9, The gene ATP8A2 has a mutation status of I126N, The gene LRRC63 has a mutation status of P159L, The gene CIPC has a mutation status of T380I, The gene ITPKA has a mutation status of M10L, The gene TYRO3 has a mutation status of A325PfsTer25, The gene MAP1A has a mutation status of E860Q, The gene GTF2A2 has a mutation status of V90M, The gene WDR93 has a mutation status of P257L, The gene WWOX has a mutation status of D58H, The gene SPEM2 has a mutation status of H131R, The gene DNAH9 has a mutation status of L173I, The gene MMP28 has a mutation status of P453S, The gene KRTAP4-7 has a mutation status of L121V, The gene HSF5 has a mutation status of T75S, The gene INTS2 has a mutation status of E191SfsTer2, The gene ABCA8 has a mutation status of M62I, The gene ENDOV has a mutation status of P235L, The gene ASPSCR1 has a mutation status of E331V, The gene PTPRM has a mutation status of Q885E, The gene GAREM1 has a mutation status of S780F, The gene SETBP1 has a mutation status of P558L, The gene ONECUT2 has a mutation status of E216K, The gene CAMSAP3 has a mutation status of M1?, The gene USHBP1 has a mutation status of G467E, The gene ZNF723 has a mutation status of C371S, The gene PROSER3 has a mutation status of P534S, The gene CGB7 has a mutation status of C54W, The gene ZNF415 has a mutation status of L511C, The gene LILRA2 has a mutation status of N201R, The gene ZAP70 has a mutation status of V470F, The gene SULT1C4 has a mutation status of H299Y, The gene CYTIP has a mutation status of I42S, The gene SCN3A has a mutation status of S665L, The gene SCN1A has a mutation status of R568Q, The gene XIRP2 has a mutation status of S2471R, The gene TTN has a mutation status of L23972PfsTer15, The gene TTN has a mutation status of W8784Ter, The gene ZNF804A has a mutation status of P1193S, The gene HECW2 has a mutation status of G216E, The gene SCYGR2 has a mutation status of H97S, The gene DNER has a mutation status of E541Q, The gene INPP5D has a mutation status of H753Y, The gene BPIFB3 has a mutation status of H426R, The gene EPB41L1 has a mutation status of G549S, The gene MYL9 has a mutation status of I49T, The gene NFATC2 has a mutation status of G108S, The gene CECR2 has a mutation status of S436F, The gene FGD5 has a mutation status of M823I, The gene BSN has a mutation status of L2311I, The gene RBM5 has a mutation status of K721SfsTer11, The gene RBM5 has a mutation status of P720H, The gene DNAH12 has a mutation status of L1060S, The gene STXBP5L has a mutation status of G299E, The gene CHRD has a mutation status of E500K, The gene ATP13A5 has a mutation status of W57Ter, The gene MUC4 has a mutation status of G3564_Q3565insHATPLPVTDTSSASTGDTTPLPVTDASSASTG, The gene BEND4 has a mutation status of I17L, The gene MTHFD2L has a mutation status of I143R, The gene CCDC158 has a mutation status of E206K, The gene ADH1A has a mutation status of S342L, The gene TLL1 has a mutation status of S932F, The gene FBXO8 has a mutation status of R219C, The gene MYO10 has a mutation status of L1851SfsTer25, The gene NIPBL has a mutation status of T2731S, The gene DDX4 has a mutation status of P165S, The gene MAST4 has a mutation status of E2456K, The gene RIPK1 has a mutation status of A569V, The gene H2BC12 has a mutation status of T53A, The gene MUC21 has a mutation status of S306R, The gene ADGRF5 has a mutation status of P413L, The gene PHIP has a mutation status of T667I, The gene BCKDHB has a mutation status of Q267Ter, The gene NPSR1 has a mutation status of V124I, The gene ABCA13 has a mutation status of I3759N, The gene MUC3A has a mutation status of P2711S, The gene BRAF has a mutation status of V600E, The gene TRBV7-9 has a mutation status of E63A, The gene KRBA1 has a mutation status of D119N, The gene GIMAP8 has a mutation status of S21L, The gene MPDZ has a mutation status of E702M, The gene UNC13B has a mutation status of P2950S, The gene OR13C2 has a mutation status of H20P, The gene ECPAS has a mutation status of R1265Ter, The gene MED12 has a mutation status of E33K, The gene TCEAL5 has a mutation status of P42L, The gene SERPINA7 has a mutation status of P383L, The gene APLN has a mutation status of L17V, The gene SLITRK4 has a mutation status of G515W	SKCM
The gene CCNL2 has a mutation status of R234Q, The gene RERE has a mutation status of D662Y, The gene CSMD2 has a mutation status of S575F, The gene TSPAN2 has a mutation status of A213P, The gene HJV has a mutation status of E302Q, The gene TRIM46 has a mutation status of Q134H, The gene GON4L has a mutation status of S1093C, The gene NES has a mutation status of Q408K, The gene ATF6 has a mutation status of S222N, The gene SLC9C2 has a mutation status of F667S, The gene IER5 has a mutation status of R194G, The gene RBBP5 has a mutation status of E523Ter, The gene CDC42BPA has a mutation status of G1143E, The gene SKIDA1 has a mutation status of A234_A244del, The gene RBP3 has a mutation status of P308A, The gene WDFY4 has a mutation status of L2974F, The gene LRRTM3 has a mutation status of E492D, The gene PSAP has a mutation status of S112F, The gene MYOZ1 has a mutation status of V67M, The gene ZNF503 has a mutation status of S321F, The gene DNMBP has a mutation status of S773C, The gene SEC31B has a mutation status of V881I, The gene C10orf120 has a mutation status of C48F, The gene TEX36 has a mutation status of R16G, The gene DPYSL4 has a mutation status of S147R, The gene OR52H1 has a mutation status of D123H, The gene OR52B6 has a mutation status of S131C, The gene NELL1 has a mutation status of A491V, The gene TRIM77 has a mutation status of L111del, The gene DDX10 has a mutation status of R331Q, The gene NXPE2 has a mutation status of M335NfsTer8, The gene GRAMD1B has a mutation status of Y573C, The gene ROBO3 has a mutation status of Q455L, The gene PRB4 has a mutation status of P237H, The gene EPS8 has a mutation status of P626S, The gene CAPZA3 has a mutation status of R188T, The gene PPFIBP1 has a mutation status of E263K, The gene RESF1 has a mutation status of K1349N, The gene TMEM117 has a mutation status of G61E, The gene DBX2 has a mutation status of P50S, The gene ZNF641 has a mutation status of R35L, The gene CERS5 has a mutation status of D351N, The gene DIP2B has a mutation status of G442A, The gene FIGNL2 has a mutation status of F477L, The gene ZNF740 has a mutation status of R146C, The gene OR10A7 has a mutation status of R89W, The gene ERBB3 has a mutation status of D857N, The gene OS9 has a mutation status of E100Q, The gene TPH2 has a mutation status of K429R, The gene DEPDC4 has a mutation status of P449A, The gene ANO4 has a mutation status of G815W, The gene TRPV4 has a mutation status of S417L, The gene OAS1 has a mutation status of R295S, The gene NUP58 has a mutation status of G31A, The gene IPO5 has a mutation status of D171H, The gene ITGBL1 has a mutation status of G377A, The gene COL4A1 has a mutation status of P96L, The gene MCF2L has a mutation status of L255F, The gene RPGRIP1 has a mutation status of E489K, The gene CDH24 has a mutation status of E135RfsTer44, The gene DHRS4 has a mutation status of G250F, The gene NFATC4 has a mutation status of S217L, The gene FOXG1 has a mutation status of G125C, The gene SCFD1 has a mutation status of A131G, The gene FBXO34 has a mutation status of A223P, The gene ATG2B has a mutation status of E232D, The gene AHNAK2 has a mutation status of N2143D, The gene MGA has a mutation status of D2606YfsTer3, The gene PLA2G4E has a mutation status of L511M, The gene COPS2 has a mutation status of S26C, The gene RNF111 has a mutation status of S267C, The gene ADAMTS17 has a mutation status of G420A, The gene XYLT1 has a mutation status of H702Q, The gene APOBR has a mutation status of S1008F, The gene KCTD19 has a mutation status of R124K, The gene ZFHX3 has a mutation status of G1925V, The gene TP53 has a mutation status of E204Ter, The gene CCDC42 has a mutation status of E52Q, The gene RAI1 has a mutation status of S502R, The gene NLE1 has a mutation status of Y261Ter, The gene KRT15 has a mutation status of F89_G96del, The gene CAVIN1 has a mutation status of N262K, The gene ADAM11 has a mutation status of L305F, The gene PLEKHM1 has a mutation status of R628G, The gene ABCC3 has a mutation status of N1181D, The gene NHERF1 has a mutation status of E139Q, The gene RECQL5 has a mutation status of D572N, The gene DLGAP1 has a mutation status of R403Q, The gene DSC3 has a mutation status of I577R, The gene SMAD4 has a mutation status of D351H, The gene CCBE1 has a mutation status of A147S, The gene UPF1 has a mutation status of P48S, The gene ZNF257 has a mutation status of C126H, The gene TSHZ3 has a mutation status of H168N, The gene ZNF568 has a mutation status of V404L, The gene WDR87 has a mutation status of Q1497E, The gene SLC8A2 has a mutation status of E332Q, The gene LILRA6 has a mutation status of Q350_F351insGY, The gene ZSCAN4 has a mutation status of Q51R, The gene MYT1L has a mutation status of D198N, The gene LRATD1 has a mutation status of E190Q, The gene RAD51AP2 has a mutation status of P118S, The gene KCNS3 has a mutation status of T85P, The gene CAMKMT has a mutation status of I205V, The gene NRXN1 has a mutation status of A1421E, The gene ARHGAP25 has a mutation status of S534I, The gene KCMF1 has a mutation status of T43A, The gene MRPS9 has a mutation status of V241M, The gene ANAPC1 has a mutation status of R40C, The gene DPP10 has a mutation status of V730G, The gene DDX18 has a mutation status of T190S, The gene MARCO has a mutation status of D84Y, The gene LRP1B has a mutation status of S4007C, The gene SLC4A10 has a mutation status of E908Ter, The gene CDCA7 has a mutation status of I201M, The gene TTN has a mutation status of W28102Ter, The gene TTN has a mutation status of P26474A, The gene TTN has a mutation status of E23170D, The gene TTN has a mutation status of P14680A, The gene TTN has a mutation status of V8331_S8335delinsA, The gene TTN has a mutation status of D8330MfsTer37, The gene TTN has a mutation status of C7681S, The gene CCDC141 has a mutation status of D641H, The gene MARS2 has a mutation status of R592W, The gene ZDBF2 has a mutation status of S1716C, The gene MAP2 has a mutation status of E255K, The gene MAP2 has a mutation status of L578F, The gene USP37 has a mutation status of F946L, The gene PPP1R16B has a mutation status of H284D, The gene CHD6 has a mutation status of R2035T, The gene PLTP has a mutation status of F4L, The gene GABPA has a mutation status of R336G, The gene IFNGR2 has a mutation status of Q290H, The gene ERG has a mutation status of G337R, The gene ZNF74 has a mutation status of Q238H, The gene ASCC2 has a mutation status of Q646E, The gene PNPLA3 has a mutation status of E467Q, The gene CTNNB1 has a mutation status of G245A, The gene FYCO1 has a mutation status of R731W, The gene SENP7 has a mutation status of D578H, The gene TRAT1 has a mutation status of E76K, The gene GATA2 has a mutation status of S54W, The gene COL6A5 has a mutation status of G1698R, The gene CEP63 has a mutation status of Q422E, The gene DZIP1L has a mutation status of S651F, The gene P2RY12 has a mutation status of M47I, The gene PHC3 has a mutation status of D791E, The gene EIF4G1 has a mutation status of H582N, The gene MUC4 has a mutation status of V2825A, The gene MUC4 has a mutation status of D1461S, The gene PCGF3 has a mutation status of N124S, The gene NSD2 has a mutation status of D560H, The gene FAM200B has a mutation status of E551K, The gene TMEM165 has a mutation status of T220S, The gene TMPRSS11D has a mutation status of A267S, The gene ABCG2 has a mutation status of S261L, The gene STOX2 has a mutation status of T839N, The gene SPEF2 has a mutation status of K442E, The gene TTC33 has a mutation status of I100L, The gene ERCC8 has a mutation status of Q326H, The gene NSA2 has a mutation status of V224E, The gene APC has a mutation status of Q1367Ter, The gene ANKHD1 has a mutation status of T1954I, The gene PCDHB3 has a mutation status of P245L, The gene PCDHB9 has a mutation status of R652C, The gene HRH2 has a mutation status of A253V, The gene CPLX2 has a mutation status of E114K, The gene CDHR2 has a mutation status of E1115K, The gene ZFP62 has a mutation status of I801V, The gene RIPK1 has a mutation status of A569V, The gene TNXB has a mutation status of M755I, The gene CMTR1 has a mutation status of L389F, The gene EPHA7 has a mutation status of E884A, The gene ROS1 has a mutation status of Q1431K, The gene AKAP12 has a mutation status of G67S, The gene VIP has a mutation status of Q8H, The gene TRGV4 has a mutation status of T40S, The gene ABCA13 has a mutation status of R3589I, The gene DOCK4 has a mutation status of L150F, The gene AASS has a mutation status of A871T, The gene MKLN1 has a mutation status of D493H, The gene TRBJ1-1 has a mutation status of A5V, The gene CUL1 has a mutation status of Y228C, The gene KMT2C has a mutation status of G2579D, The gene KMT2C has a mutation status of S2472G, The gene MYOM2 has a mutation status of V1376M, The gene PXDNL has a mutation status of W1233L, The gene TRPA1 has a mutation status of E223Ter, The gene OR13D1 has a mutation status of G138E, The gene PAPPA has a mutation status of E1202V, The gene CRB2 has a mutation status of S374R, The gene NR6A1 has a mutation status of E427K, The gene NUP214 has a mutation status of R854Q, The gene SARDH has a mutation status of A479P, The gene MT-ND4 has a mutation status of F411L, The gene MT-ND5 has a mutation status of T449A, The gene NUDT11 has a mutation status of P42L, The gene HDX has a mutation status of W98Ter, The gene RAB40AL has a mutation status of G26R, The gene CLIC2 has a mutation status of M38R	COAD
The gene PER3 has a mutation status of C510Y, The gene SDHB has a mutation status of A262LfsTer8, The gene AHDC1 has a mutation status of R73P, The gene FGR has a mutation status of D353N, The gene ZFYVE9 has a mutation status of S314N, The gene DENND2D has a mutation status of W111_A112delinsTer, The gene SPAG17 has a mutation status of T1392S, The gene FMO5 has a mutation status of D492G, The gene CHD1L has a mutation status of L294F, The gene VPS45 has a mutation status of N289IfsTer17, The gene TCHHL1 has a mutation status of V516L, The gene EFNA3 has a mutation status of K125T, The gene IFI16 has a mutation status of H757N, The gene AIM2 has a mutation status of K39Q, The gene PAPPA2 has a mutation status of K319N, The gene HMCN1 has a mutation status of G4042D, The gene RGS2 has a mutation status of Y47C, The gene RGS2 has a mutation status of F48Y, The gene CFHR4 has a mutation status of E245A, The gene PTPN7 has a mutation status of D178N, The gene USH2A has a mutation status of Y3701H, The gene TMEM63A has a mutation status of C315G, The gene GNPAT has a mutation status of L169R, The gene MTR has a mutation status of L646F, The gene KLF6 has a mutation status of V210AfsTer4, The gene SFMBT2 has a mutation status of V491L, The gene TAF3 has a mutation status of Q222Ter, The gene ANKRD26 has a mutation status of K7Ter, The gene JMJD1C has a mutation status of N1181S, The gene SLC29A3 has a mutation status of F146V, The gene VCL has a mutation status of I384T, The gene CHUK has a mutation status of Q616R, The gene ADRA2A has a mutation status of P270L, The gene PLEKHA1 has a mutation status of S398R, The gene MUC6 has a mutation status of T1854I, The gene MRGPRX1 has a mutation status of R207G, The gene NDUFS8 has a mutation status of P132SfsTer2, The gene GAB2 has a mutation status of M438Ter, The gene DCP1B has a mutation status of I515N, The gene SLCO1B3 has a mutation status of V349I, The gene LRRK2 has a mutation status of S1345I, The gene SLC38A4 has a mutation status of E179Q, The gene ZNF740 has a mutation status of L144P, The gene ITGB7 has a mutation status of C654Y, The gene ZNF385A has a mutation status of P275T, The gene AVIL has a mutation status of E240G, The gene CUX2 has a mutation status of A1186T, The gene RPL6 has a mutation status of M1?, The gene RNF10 has a mutation status of G665W, The gene PABPC3 has a mutation status of L38H, The gene WASF3 has a mutation status of F371V, The gene RBM26 has a mutation status of P540H, The gene SLITRK5 has a mutation status of K742N, The gene MBNL2 has a mutation status of H249N, The gene OR4Q3 has a mutation status of L113I, The gene SALL2 has a mutation status of P756T, The gene HECTD1 has a mutation status of R1058K, The gene DLGAP5 has a mutation status of Q635Ter, The gene SYNE2 has a mutation status of E4681Q, The gene HSPA2 has a mutation status of T422M, The gene LTBP2 has a mutation status of N421I, The gene ADCK1 has a mutation status of D403H, The gene TTC8 has a mutation status of W12Ter, The gene COX8C has a mutation status of P38S, The gene DYNC1H1 has a mutation status of M2779V, The gene HERC2 has a mutation status of A199T, The gene DISP2 has a mutation status of I180V, The gene IVD has a mutation status of G279W, The gene BAHD1 has a mutation status of P410R, The gene TYRO3 has a mutation status of A323_S324insTPA, The gene PLA2G4D has a mutation status of T767A, The gene TBC1D21 has a mutation status of S196N, The gene CYP11A1 has a mutation status of G494S, The gene SCAPER has a mutation status of Q866P, The gene DET1 has a mutation status of K433T, The gene CLCN7 has a mutation status of M349I, The gene SLC5A11 has a mutation status of D14H, The gene CLN3 has a mutation status of L426Q, The gene GNAO1 has a mutation status of F336I, The gene SLC12A3 has a mutation status of Q1021K, The gene CES2 has a mutation status of G180S, The gene CARMIL2 has a mutation status of A450S, The gene PKD1L2 has a mutation status of D37Y, The gene COTL1 has a mutation status of T80A, The gene ABR has a mutation status of H507R, The gene SPNS2 has a mutation status of A52T, The gene ZNF18 has a mutation status of E110D, The gene MRM1 has a mutation status of G194W, The gene FBXO47 has a mutation status of L59F, The gene GJD3 has a mutation status of H175Y, The gene FKBP10 has a mutation status of L430RfsTer49, The gene CNTD1 has a mutation status of R100K, The gene BRCA1 has a mutation status of V1687F, The gene EPN3 has a mutation status of D344E, The gene RAD51C has a mutation status of F229L, The gene HEATR6 has a mutation status of S531A, The gene TANC2 has a mutation status of L299F, The gene MAP3K3 has a mutation status of Q256R, The gene DNAH17 has a mutation status of E597D, The gene CCDC40 has a mutation status of K438Q, The gene FN3KRP has a mutation status of G152R, The gene ATP8B1 has a mutation status of D12E, The gene SERPINB8 has a mutation status of A89G, The gene ZNF516 has a mutation status of H767L, The gene SALL3 has a mutation status of S914N, The gene NOTCH3 has a mutation status of A1948P, The gene ISYNA1 has a mutation status of T434A, The gene ZNF708 has a mutation status of C506S, The gene HNRNPL has a mutation status of H339Y, The gene CYP2A7 has a mutation status of R485Ter, The gene TGFB1 has a mutation status of W17Ter, The gene KLK1 has a mutation status of V92A, The gene ZNF808 has a mutation status of H306L, The gene ZFP28 has a mutation status of L39_A40delinsFS, The gene ZNF71 has a mutation status of T290HfsTer312, The gene VN1R1 has a mutation status of L173F, The gene SNTG2 has a mutation status of E245Q, The gene GEN1 has a mutation status of I789M, The gene WDR35 has a mutation status of M99IfsTer11, The gene APOB has a mutation status of S1162T, The gene ADGRF3 has a mutation status of R571S, The gene TSPYL6 has a mutation status of P92T, The gene EHBP1 has a mutation status of R827C, The gene PLEK has a mutation status of R293G, The gene RNF103 has a mutation status of R407GfsTer25, The gene SNRNP200 has a mutation status of I993M, The gene MAP4K4 has a mutation status of K41M, The gene TGFBRAP1 has a mutation status of F361L, The gene ST6GAL2 has a mutation status of S44Y, The gene SH3RF3 has a mutation status of I324N, The gene MAP3K19 has a mutation status of L903QfsTer29, The gene ZRANB3 has a mutation status of S159L, The gene SCN9A has a mutation status of L75P, The gene DYNC1I2 has a mutation status of A431P, The gene NFE2L2 has a mutation status of G81S, The gene SPEG has a mutation status of E120D, The gene INPP5D has a mutation status of R167Ter, The gene LRRFIP1 has a mutation status of M3L, The gene GPC1 has a mutation status of Q351K, The gene ZNF133 has a mutation status of G362V, The gene HNF4A has a mutation status of G418S, The gene DDX27 has a mutation status of A657T, The gene ZFP64 has a mutation status of E575V, The gene CASS4 has a mutation status of A18G, The gene FAM209A has a mutation status of H96L, The gene HELZ2 has a mutation status of W1062Ter, The gene TNFRSF6B has a mutation status of C126F, The gene BACH1 has a mutation status of F130I, The gene TIAM1 has a mutation status of K579N, The gene CSTB has a mutation status of A14S, The gene LZTR1 has a mutation status of Q319RfsTer32, The gene ZNF280B has a mutation status of D275E, The gene EMID1 has a mutation status of G217S, The gene TNRC6B has a mutation status of T274S, The gene CAND2 has a mutation status of V839F, The gene KCNH8 has a mutation status of A463V, The gene PDCD6IP has a mutation status of P816L, The gene SETD2 has a mutation status of D1537VfsTer28, The gene SETD2 has a mutation status of N1535K, The gene COL7A1 has a mutation status of A1397D, The gene AMT has a mutation status of H139Y, The gene CCDC66 has a mutation status of S90T, The gene LRIG1 has a mutation status of R982T, The gene DCBLD2 has a mutation status of Y732F, The gene CCDC191 has a mutation status of L450IfsTer7, The gene TEX55 has a mutation status of T114A, The gene TIMMDC1 has a mutation status of R220S, The gene CD80 has a mutation status of F93C, The gene SLC15A2 has a mutation status of K110Q, The gene SLC41A3 has a mutation status of I370S, The gene ATR has a mutation status of T2641I, The gene SMC4 has a mutation status of E292V, The gene PIK3CA has a mutation status of E545G, The gene APOD has a mutation status of K176E, The gene LMLN has a mutation status of R80G, The gene NSD2 has a mutation status of A965P, The gene CC2D2A has a mutation status of E241V, The gene DHX15 has a mutation status of K132R, The gene AFF1 has a mutation status of D1031H, The gene INTS12 has a mutation status of P244S, The gene PRDM5 has a mutation status of T222P, The gene ELMOD2 has a mutation status of N82IfsTer14, The gene INPP4B has a mutation status of P789L, The gene FGG has a mutation status of I262M, The gene ICE1 has a mutation status of K209M, The gene SPEF2 has a mutation status of S1667G, The gene NIPBL has a mutation status of Q2311L, The gene IQGAP2 has a mutation status of C439Y, The gene PDE8B has a mutation status of D142Y, The gene MEF2C has a mutation status of L277EfsTer6, The gene PCSK1 has a mutation status of G236A, The gene SLC22A4 has a mutation status of I89P, The gene PKD2L2 has a mutation status of I172N, The gene PCDHGA2 has a mutation status of E282K, The gene SH3PXD2B has a mutation status of N22H, The gene NQO2 has a mutation status of G3D, The gene H4C2 has a mutation status of R96L, The gene HLA-DQB2 has a mutation status of V37Y, The gene BRD2 has a mutation status of Y702C, The gene DEFB113 has a mutation status of T25P, The gene ZNF292 has a mutation status of F1944L, The gene HACE1 has a mutation status of N74I, The gene SOBP has a mutation status of D811N, The gene WASF1 has a mutation status of H524P, The gene UTRN has a mutation status of K2159N, The gene FBXO30 has a mutation status of I467M, The gene AGPAT4 has a mutation status of S340R, The gene RBAK has a mutation status of I446L, The gene ACTB has a mutation status of V54G, The gene RNF216 has a mutation status of M558V, The gene BZW2 has a mutation status of E281G, The gene NT5C3A has a mutation status of V244L, The gene COBL has a mutation status of L368P, The gene RSBN1L has a mutation status of G386R, The gene SEMA3E has a mutation status of I436G, The gene TRRAP has a mutation status of F1412C, The gene MUC17 has a mutation status of S2003N, The gene CTTNBP2 has a mutation status of S475P, The gene CNTNAP2 has a mutation status of F497I, The gene CUL1 has a mutation status of K93N, The gene NOS3 has a mutation status of R202K, The gene CLDN23 has a mutation status of S87Ter, The gene DOCK5 has a mutation status of G134V, The gene KCTD9 has a mutation status of A373T, The gene PRKDC has a mutation status of R4082Ter, The gene PXDNL has a mutation status of T514I, The gene RB1CC1 has a mutation status of V1264L, The gene CHD7 has a mutation status of N2518T, The gene KLF10 has a mutation status of R391G, The gene NRBP2 has a mutation status of V445E, The gene RANBP6 has a mutation status of D221G, The gene RPS6 has a mutation status of R198H, The gene SLC24A2 has a mutation status of V646M, The gene TLE4 has a mutation status of Y370Ter, The gene PAPPA has a mutation status of N1141Y, The gene GARNL3 has a mutation status of N202H, The gene SURF6 has a mutation status of R339H, The gene MT-ND5 has a mutation status of F478L, The gene MT-ND6 has a mutation status of N174IfsTer?, The gene PPP2R3B has a mutation status of S24I, The gene PPP2R3B has a mutation status of Y21N, The gene REPS2 has a mutation status of P414A, The gene APOO has a mutation status of L103P, The gene CYBB has a mutation status of C369F, The gene HUWE1 has a mutation status of G3295C, The gene DLG3 has a mutation status of T577N, The gene MAGEE1 has a mutation status of I884T, The gene SLITRK4 has a mutation status of P610T, The gene AGRN has a mutation status of S330QfsTer12, The gene AGRN has a mutation status of S330I, The gene PER3 has a mutation status of C510Y, The gene DDI2 has a mutation status of E385_A386insVAE, The gene SDHB has a mutation status of A262LfsTer8, The gene FGR has a mutation status of D353N, The gene PTPRF has a mutation status of L431M, The gene ZFYVE9 has a mutation status of S314N, The gene DENND2D has a mutation status of W111_A112delinsTer, The gene SPAG17 has a mutation status of T1392S, The gene FMO5 has a mutation status of D492G, The gene CHD1L has a mutation status of L294F, The gene VPS45 has a mutation status of N289IfsTer17, The gene TCHHL1 has a mutation status of V516L, The gene EFNA3 has a mutation status of K125T, The gene IFI16 has a mutation status of H757N, The gene AIM2 has a mutation status of K39Q, The gene PAPPA2 has a mutation status of K319N, The gene RGS2 has a mutation status of Y47C, The gene RGS2 has a mutation status of F48Y, The gene CFHR4 has a mutation status of E245A, The gene CFHR4 has a mutation status of Q361H, The gene PTPN7 has a mutation status of D178N, The gene USH2A has a mutation status of Y3701H, The gene TMEM63A has a mutation status of C315G, The gene LEFTY1 has a mutation status of G156D, The gene FAM89A has a mutation status of R75Q, The gene GNPAT has a mutation status of L169R, The gene MTR has a mutation status of L646F, The gene RYR2 has a mutation status of A118S, The gene OR2C3 has a mutation status of M186I, The gene KLF6 has a mutation status of V210AfsTer4, The gene SFMBT2 has a mutation status of V491L, The gene JMJD1C has a mutation status of N1181S, The gene CCAR1 has a mutation status of D944H, The gene SLC29A3 has a mutation status of F146V, The gene ECD has a mutation status of C146Y, The gene VCL has a mutation status of I384T, The gene CHUK has a mutation status of Q616R, The gene PLEKHA1 has a mutation status of S398R, The gene INPP5A has a mutation status of A2_?3, The gene DNHD1 has a mutation status of S1100I, The gene MRGPRX1 has a mutation status of R207G, The gene KLC2 has a mutation status of Y346F, The gene NDUFS8 has a mutation status of P132SfsTer2, The gene GAB2 has a mutation status of M438Ter, The gene SLC36A4 has a mutation status of V132L, The gene IQSEC3 has a mutation status of Q1017R, The gene DCP1B has a mutation status of I515N, The gene CACNA1C has a mutation status of H2030Y, The gene TAS2R13 has a mutation status of E61K, The gene SLCO1B3 has a mutation status of V349I, The gene LRRK2 has a mutation status of S1345I, The gene MUC19 has a mutation status of P3149S, The gene SLC38A4 has a mutation status of E179Q, The gene ITGB7 has a mutation status of C654Y, The gene MBD6 has a mutation status of A224S, The gene AVIL has a mutation status of E240G, The gene PTPRB has a mutation status of Q1349Ter, The gene CUX2 has a mutation status of A1186T, The gene RPL6 has a mutation status of M1?, The gene RNF10 has a mutation status of G665W, The gene ADGRD1 has a mutation status of K322R, The gene NBEA has a mutation status of K1275Ter, The gene NBEA has a mutation status of W2289Ter, The gene RBM26 has a mutation status of P540H, The gene MYO16 has a mutation status of L1142V, The gene OR4Q3 has a mutation status of L113I, The gene SALL2 has a mutation status of P756T, The gene HECTD1 has a mutation status of R1058K, The gene DLGAP5 has a mutation status of Q635Ter, The gene SYNE2 has a mutation status of E4681Q, The gene HSPA2 has a mutation status of T422M, The gene ADCK1 has a mutation status of D403H, The gene TTC8 has a mutation status of W12Ter, The gene COX8C has a mutation status of P38S, The gene UNC79 has a mutation status of D1728N, The gene BCL11B has a mutation status of P268T, The gene DYNC1H1 has a mutation status of M2779V, The gene HERC2 has a mutation status of A199T, The gene DISP2 has a mutation status of I180V, The gene IVD has a mutation status of G279W, The gene BAHD1 has a mutation status of P410R, The gene PLA2G4D has a mutation status of T767A, The gene ITGA11 has a mutation status of H275Q, The gene HCN4 has a mutation status of I48M, The gene CYP11A1 has a mutation status of G494S, The gene SCAPER has a mutation status of Q866P, The gene DET1 has a mutation status of K433T, The gene RHBDL1 has a mutation status of F350L, The gene SLC5A11 has a mutation status of D14H, The gene CLN3 has a mutation status of L426Q, The gene PAGR1 has a mutation status of P137H, The gene GNAO1 has a mutation status of F336I, The gene SLC12A3 has a mutation status of Q1021K, The gene CES2 has a mutation status of G180S, The gene CDYL2 has a mutation status of M1?, The gene PKD1L2 has a mutation status of D37Y, The gene COTL1 has a mutation status of T80A, The gene ABR has a mutation status of H507R, The gene ZNF18 has a mutation status of E110D, The gene MRM1 has a mutation status of G194W, The gene FBXO47 has a mutation status of L59F, The gene GJD3 has a mutation status of H175Y, The gene GJD3 has a mutation status of F70I, The gene FKBP10 has a mutation status of L430RfsTer49, The gene CNTD1 has a mutation status of R100K, The gene BRCA1 has a mutation status of V1687F, The gene EPN3 has a mutation status of D344E, The gene RAD51C has a mutation status of F229L, The gene HEATR6 has a mutation status of S531A, The gene BRIP1 has a mutation status of E1104Q, The gene MAP3K3 has a mutation status of Q256R, The gene DNAH17 has a mutation status of E597D, The gene CCDC40 has a mutation status of K438Q, The gene RMC1 has a mutation status of G220E, The gene ZNF397 has a mutation status of G291W, The gene SERPINB8 has a mutation status of A89G, The gene ZNF516 has a mutation status of H767L, The gene SALL3 has a mutation status of A185L, The gene SALL3 has a mutation status of S914N, The gene ABCA7 has a mutation status of K411N, The gene ZFR2 has a mutation status of C328Ter, The gene PEX11G has a mutation status of W205C, The gene NOTCH3 has a mutation status of A1948P, The gene NOTCH3 has a mutation status of S310T, The gene ISYNA1 has a mutation status of T434A, The gene ZNF708 has a mutation status of C506S, The gene GPI has a mutation status of P201T, The gene HNRNPL has a mutation status of H339Y, The gene LTBP4 has a mutation status of P455A, The gene CYP2A7 has a mutation status of R485Ter, The gene BCL3 has a mutation status of G86Ter, The gene KLK1 has a mutation status of V92A, The gene ZNF808 has a mutation status of H306L, The gene ZFP28 has a mutation status of L39_A40delinsFS, The gene VN1R1 has a mutation status of L173F, The gene SNTG2 has a mutation status of E245Q, The gene GEN1 has a mutation status of I789M, The gene WDR35 has a mutation status of M99IfsTer11, The gene APOB has a mutation status of S1162T, The gene BIRC6 has a mutation status of Q1158L, The gene BIRC6 has a mutation status of H1159P, The gene CYP1B1 has a mutation status of V178L, The gene TSPYL6 has a mutation status of P92T, The gene EHBP1 has a mutation status of R827C, The gene SNRNP200 has a mutation status of I993M, The gene MAP4K4 has a mutation status of K41M, The gene TGFBRAP1 has a mutation status of F361L, The gene ST6GAL2 has a mutation status of S44Y, The gene MAP3K19 has a mutation status of L903QfsTer29, The gene LRP1B has a mutation status of D2962Ter, The gene LRP1B has a mutation status of D2961delinsVLTer, The gene ZEB2 has a mutation status of S61R, The gene KIF5C has a mutation status of E659G, The gene SCN9A has a mutation status of L75P, The gene DYNC1I2 has a mutation status of A431P, The gene NFE2L2 has a mutation status of G81S, The gene CCNYL1 has a mutation status of D263Y, The gene INPP5D has a mutation status of R167Ter, The gene SNED1 has a mutation status of P61Q, The gene ZNF133 has a mutation status of G362V, The gene DZANK1 has a mutation status of P263L, The gene RBL1 has a mutation status of T713I, The gene HNF4A has a mutation status of G418S, The gene DDX27 has a mutation status of A657T, The gene FAM209A has a mutation status of H96L, The gene COL20A1 has a mutation status of H598N, The gene HELZ2 has a mutation status of W1062Ter, The gene BACH1 has a mutation status of F130I, The gene TIAM1 has a mutation status of K579N, The gene CLIC6 has a mutation status of G263EfsTer34, The gene BRWD1 has a mutation status of S2070T, The gene SLC19A1 has a mutation status of R243Q, The gene LZTR1 has a mutation status of Q319RfsTer32, The gene ZNF280B has a mutation status of D275E, The gene TMPRSS6 has a mutation status of S343G, The gene TNRC6B has a mutation status of T274S, The gene EFCAB6 has a mutation status of P365S, The gene DENND6B has a mutation status of S444N, The gene SBF1 has a mutation status of E366D, The gene CAND2 has a mutation status of V839F, The gene PDCD6IP has a mutation status of P816L, The gene SETD2 has a mutation status of D1537VfsTer28, The gene SETD2 has a mutation status of N1535K, The gene AMT has a mutation status of H139Y, The gene LRTM1 has a mutation status of Q98H, The gene CCDC66 has a mutation status of S90T, The gene LRIG1 has a mutation status of R982T, The gene CHMP2B has a mutation status of D148G, The gene DCBLD2 has a mutation status of Y732F, The gene NECTIN3 has a mutation status of G144V, The gene CCDC191 has a mutation status of L450IfsTer7, The gene TIMMDC1 has a mutation status of R220S, The gene CD80 has a mutation status of F93C, The gene SLC15A2 has a mutation status of K110Q, The gene SLC41A3 has a mutation status of I370S, The gene NPHP3 has a mutation status of E192K, The gene ATR has a mutation status of T2641I, The gene SMC4 has a mutation status of E292V, The gene PIK3CA has a mutation status of E545G, The gene NDUFB5 has a mutation status of Q141H, The gene APOD has a mutation status of K176E, The gene LMLN has a mutation status of R80G, The gene NSD2 has a mutation status of A965P, The gene CC2D2A has a mutation status of E241V, The gene DHX15 has a mutation status of K132R, The gene NWD2 has a mutation status of D1376H, The gene AFF1 has a mutation status of D1031H, The gene INTS12 has a mutation status of P244S, The gene PRDM5 has a mutation status of T222P, The gene ELMOD2 has a mutation status of N82IfsTer14, The gene INPP4B has a mutation status of P789L, The gene FGG has a mutation status of I262M, The gene ADAMTS16 has a mutation status of Q148Ter, The gene ICE1 has a mutation status of K209M, The gene SPEF2 has a mutation status of S1667G, The gene NIPBL has a mutation status of Q2311L, The gene IQGAP2 has a mutation status of C439Y, The gene MEF2C has a mutation status of L277EfsTer6, The gene PCSK1 has a mutation status of G236A, The gene PKD2L2 has a mutation status of I172N, The gene PCDHGA2 has a mutation status of E282K, The gene PDLIM7 has a mutation status of Q131Ter, The gene H4C2 has a mutation status of R96L, The gene BRD2 has a mutation status of Y702C, The gene CUL9 has a mutation status of N1627K, The gene DEFB113 has a mutation status of T25P, The gene ZNF292 has a mutation status of F1944L, The gene FHL5 has a mutation status of P47Q, The gene HACE1 has a mutation status of N74I, The gene SOBP has a mutation status of D811N, The gene FBXO30 has a mutation status of I467M, The gene AGPAT4 has a mutation status of S340R, The gene RBAK has a mutation status of I446L, The gene ACTB has a mutation status of V54G, The gene RNF216 has a mutation status of M558V, The gene RNF216 has a mutation status of S418F, The gene BZW2 has a mutation status of E281G, The gene NT5C3A has a mutation status of V244L, The gene RSBN1L has a mutation status of G386R, The gene SEMA3E has a mutation status of I436G, The gene TRRAP has a mutation status of F1412C, The gene MUC17 has a mutation status of S2003N, The gene CTTNBP2 has a mutation status of S475P, The gene STRA8 has a mutation status of S244AfsTer30, The gene CNTNAP2 has a mutation status of F497I, The gene CUL1 has a mutation status of K93N, The gene NOS3 has a mutation status of R202K, The gene CLDN23 has a mutation status of S87Ter, The gene DOCK5 has a mutation status of G134V, The gene KCTD9 has a mutation status of A373T, The gene PRKDC has a mutation status of R4082Ter, The gene RGS20 has a mutation status of S65L, The gene CHD7 has a mutation status of N2518T, The gene VIRMA has a mutation status of P1449R, The gene KLF10 has a mutation status of R391G, The gene RANBP6 has a mutation status of D221G, The gene RPS6 has a mutation status of R198H, The gene SLC24A2 has a mutation status of V646M, The gene TLE4 has a mutation status of Y370Ter, The gene GARNL3 has a mutation status of N202H, The gene SURF6 has a mutation status of R339H, The gene MT-ND5 has a mutation status of F478L, The gene MT-ND6 has a mutation status of N174IfsTer?, The gene REPS2 has a mutation status of P414A, The gene APOO has a mutation status of L103P, The gene USP9X has a mutation status of Q51E, The gene HUWE1 has a mutation status of G3295C, The gene DLG3 has a mutation status of T577N, The gene MAGEE1 has a mutation status of I884T, The gene SLITRK4 has a mutation status of P610T, The gene DUSP9 has a mutation status of G107S	BLCA
The gene PERM1 has a mutation status of G189C, The gene CASZ1 has a mutation status of E1606Q, The gene FGR has a mutation status of A239T, The gene EPB41 has a mutation status of H16Y, The gene CSMD2 has a mutation status of D885N, The gene DAB1 has a mutation status of A294D, The gene TNNI3K has a mutation status of L386Ter, The gene TTLL7 has a mutation status of R449Q, The gene FNBP1L has a mutation status of S422Ter, The gene DPYD has a mutation status of G681C, The gene S1PR1 has a mutation status of N21K, The gene FCRL2 has a mutation status of Y332Ter, The gene FCRLA has a mutation status of Q193K, The gene ALDH9A1 has a mutation status of G160D, The gene KDM5B has a mutation status of F1077L, The gene NFASC has a mutation status of L1191P, The gene CR1 has a mutation status of S1498P, The gene OBSCN has a mutation status of A2212L, The gene TAF5L has a mutation status of P225L, The gene RYR2 has a mutation status of L3519M, The gene NLRP3 has a mutation status of R268M, The gene OR2L13 has a mutation status of P286H, The gene WDFY4 has a mutation status of Y2417H, The gene GRID1 has a mutation status of L851V, The gene HELLS has a mutation status of E743G, The gene INA has a mutation status of E185D, The gene MUC6 has a mutation status of I1653V, The gene OR5M10 has a mutation status of I49M, The gene OR9I1 has a mutation status of C107F, The gene AHNAK has a mutation status of S4220L, The gene CCDC88B has a mutation status of P244S, The gene FAT3 has a mutation status of S3067T, The gene KCNJ5 has a mutation status of G164R, The gene LRP6 has a mutation status of P1458F, The gene MUC19 has a mutation status of V2683G, The gene MUC19 has a mutation status of V4071A, The gene MUC19 has a mutation status of I6366K, The gene SCN8A has a mutation status of E1804K, The gene PHLDA1 has a mutation status of P87R, The gene GLT8D2 has a mutation status of N254D, The gene PCDH17 has a mutation status of P241S, The gene INSM2 has a mutation status of A92T, The gene UBE3A has a mutation status of L755F, The gene FMN1 has a mutation status of S272A, The gene SOX8 has a mutation status of V252M, The gene DNAH3 has a mutation status of P2357CfsTer16, The gene NFAT5 has a mutation status of A632E, The gene POLR2A has a mutation status of S1944Y, The gene TP53 has a mutation status of V218del, The gene CCDC42 has a mutation status of D211N, The gene MYH3 has a mutation status of E1057K, The gene SLC47A1 has a mutation status of H360Y, The gene NFATC1 has a mutation status of S512F, The gene P2RY11 has a mutation status of N179S, The gene ZNF99 has a mutation status of T355N, The gene CYP2F1 has a mutation status of V175R, The gene LILRA1 has a mutation status of P271R, The gene NLRP11 has a mutation status of E987G, The gene CAPN14 has a mutation status of Y182Ter, The gene CRIM1 has a mutation status of D1000E, The gene EML4 has a mutation status of K406R, The gene PTCD3 has a mutation status of I375N, The gene FER1L5 has a mutation status of G246R, The gene SLC9A2 has a mutation status of I376T, The gene SH3RF3 has a mutation status of N537I, The gene LRP2 has a mutation status of L869I, The gene TTN has a mutation status of E15828Q, The gene DOCK10 has a mutation status of V845L, The gene PLCB1 has a mutation status of D206Y, The gene RALGAPA2 has a mutation status of L1357R, The gene SLC32A1 has a mutation status of A35V, The gene ADAMTS1 has a mutation status of S134R, The gene GART has a mutation status of C93I, The gene CABIN1 has a mutation status of F463C, The gene MYO18B has a mutation status of K1825R, The gene SBF1 has a mutation status of R567H, The gene SSUH2 has a mutation status of E52G, The gene TATDN2 has a mutation status of E550K, The gene GALNT15 has a mutation status of W487C, The gene SATB1 has a mutation status of V511M, The gene SCAP has a mutation status of D1211G, The gene SCAP has a mutation status of I1209_S1210insLAHCNLCLPS, The gene LSAMP has a mutation status of Q114H, The gene CASR has a mutation status of I235N, The gene TMCC1 has a mutation status of Q59H, The gene SLITRK3 has a mutation status of R777H, The gene SLITRK3 has a mutation status of A112E, The gene IDUA has a mutation status of P357A, The gene SCFD2 has a mutation status of R195W, The gene UGT2B11 has a mutation status of A327D, The gene UGT2A2 has a mutation status of P291L, The gene GK2 has a mutation status of G320C, The gene RNF150 has a mutation status of H97Q, The gene SPEF2 has a mutation status of P1448S, The gene GRIA1 has a mutation status of G905V, The gene HLA-C has a mutation status of R132H, The gene REV3L has a mutation status of T2983I, The gene ENPP1 has a mutation status of F703L, The gene MYB has a mutation status of L300F, The gene SMOC2 has a mutation status of A292P, The gene ZMIZ2 has a mutation status of L550Q, The gene PKD1L1 has a mutation status of P272S, The gene EGFR has a mutation status of E746_A750del, The gene ZSCAN25 has a mutation status of A100T, The gene LRRN3 has a mutation status of D617N, The gene PODXL has a mutation status of D373E, The gene GBX1 has a mutation status of A361P, The gene DPP6 has a mutation status of E295Ter, The gene SOX7 has a mutation status of L103M, The gene DLC1 has a mutation status of Q917H, The gene UNC5D has a mutation status of A665P, The gene LY6L has a mutation status of L138F, The gene PRSS3 has a mutation status of G208R, The gene RUSC2 has a mutation status of S987_I988del, The gene PTCH1 has a mutation status of T314N, The gene MT-ND4 has a mutation status of N390S, The gene MT-ND4 has a mutation status of L445F, The gene MT-ND5 has a mutation status of A219V, The gene MT-ND5 has a mutation status of P265S, The gene NLGN4X has a mutation status of P111H, The gene SUPT20HL1 has a mutation status of Q649Ter, The gene ARX has a mutation status of P38S, The gene UBQLN2 has a mutation status of A469S, The gene POF1B has a mutation status of H34Y, The gene NXF3 has a mutation status of R76W, The gene WDR44 has a mutation status of P142L, The gene WDR44 has a mutation status of S143F, The gene CT47C1 has a mutation status of K293N, The gene PERM1 has a mutation status of G189C, The gene CASZ1 has a mutation status of E1606Q, The gene FGR has a mutation status of A239T, The gene EPB41 has a mutation status of H16Y, The gene CSMD2 has a mutation status of D885N, The gene FAAH has a mutation status of P424L, The gene FOXD2 has a mutation status of F295RfsTer198, The gene BTF3L4 has a mutation status of D134H, The gene C8A has a mutation status of Y172C, The gene DAB1 has a mutation status of A294D, The gene PATJ has a mutation status of D552Y, The gene TNNI3K has a mutation status of L386Ter, The gene ADGRL2 has a mutation status of T514K, The gene TTLL7 has a mutation status of R449Q, The gene CTBS has a mutation status of I302N, The gene FNBP1L has a mutation status of S422Ter, The gene DPYD has a mutation status of G681C, The gene S1PR1 has a mutation status of N21K, The gene UBAP2L has a mutation status of S707Ter, The gene CHRNB2 has a mutation status of W464Ter, The gene FCRL2 has a mutation status of Y332Ter, The gene FCRL1 has a mutation status of S287N, The gene FCRLA has a mutation status of Q193K, The gene ALDH9A1 has a mutation status of G160D, The gene DPT has a mutation status of A98P, The gene CACNA1E has a mutation status of Y1512Ter, The gene KDM5B has a mutation status of F1077L, The gene NFASC has a mutation status of L1191P, The gene CR1 has a mutation status of S1498P, The gene OBSCN has a mutation status of A2212L, The gene TAF5L has a mutation status of P225L, The gene RYR2 has a mutation status of L3519M, The gene NLRP3 has a mutation status of R268M, The gene OR2L5 has a mutation status of I68T, The gene OR2L13 has a mutation status of P286H, The gene RET has a mutation status of N723S, The gene LRRTM3 has a mutation status of L540H, The gene GRID1 has a mutation status of L851V, The gene HELLS has a mutation status of E743G, The gene INA has a mutation status of E185D, The gene OR51L1 has a mutation status of M42K, The gene DNHD1 has a mutation status of A550S, The gene ZNF214 has a mutation status of L109V, The gene OR5M10 has a mutation status of I49M, The gene OR9I1 has a mutation status of C107F, The gene OSBP has a mutation status of S43P, The gene MS4A6E has a mutation status of A43E, The gene AHNAK has a mutation status of S4220L, The gene CCDC88B has a mutation status of P244S, The gene DPP3 has a mutation status of K629M, The gene NAALAD2 has a mutation status of G417V, The gene FAT3 has a mutation status of S3067T, The gene HEPHL1 has a mutation status of K374T, The gene DYNC2H1 has a mutation status of A2152G, The gene NXPE1 has a mutation status of L230H, The gene OR8G1 has a mutation status of Y290_S291insICY, The gene KCNJ5 has a mutation status of G164R, The gene LRP6 has a mutation status of P1458F, The gene ADAMTS20 has a mutation status of T1579A, The gene ATF1 has a mutation status of A19S, The gene SCN8A has a mutation status of E1804K, The gene PHLDA1 has a mutation status of P87R, The gene EEA1 has a mutation status of V287L, The gene GLT8D2 has a mutation status of N254D, The gene DAO has a mutation status of R120EfsTer18, The gene RPH3A has a mutation status of Q293K, The gene PCDH17 has a mutation status of P241S, The gene ACTR10 has a mutation status of K191R, The gene GPR135 has a mutation status of A50S, The gene UBE3A has a mutation status of L755F, The gene FMN1 has a mutation status of S272A, The gene TYRO3 has a mutation status of V233HfsTer11, The gene C2CD4B has a mutation status of E46W, The gene PRR35 has a mutation status of E488Q, The gene SOX8 has a mutation status of V252M, The gene CACNA1H has a mutation status of L936H, The gene DNAH3 has a mutation status of P2357CfsTer16, The gene IRX6 has a mutation status of G323V, The gene NFAT5 has a mutation status of A632E, The gene AP1G1 has a mutation status of Y460C, The gene POLR2A has a mutation status of S1944Y, The gene TP53 has a mutation status of V218del, The gene MYH3 has a mutation status of E1057K, The gene SLC47A1 has a mutation status of H360Y, The gene KRT16 has a mutation status of G63R, The gene KAT2A has a mutation status of H315N, The gene DLX3 has a mutation status of W251Ter, The gene APPBP2 has a mutation status of Y226Ter, The gene RAB40B has a mutation status of P263_Q264insPRPP, The gene NFATC1 has a mutation status of S512F, The gene ABCA7 has a mutation status of G1827A, The gene DAZAP1 has a mutation status of F262del, The gene DAZAP1 has a mutation status of T263P, The gene DAZAP1 has a mutation status of A286D, The gene KDM4B has a mutation status of P511S, The gene P2RY11 has a mutation status of N179S, The gene ZNF90 has a mutation status of V98E, The gene ZNF66 has a mutation status of C539Ter, The gene ZNF99 has a mutation status of T355N, The gene ZNF723 has a mutation status of K332N, The gene ZNF615 has a mutation status of E168Q, The gene NLRP11 has a mutation status of E987G, The gene NLRP8 has a mutation status of R781S, The gene SOX11 has a mutation status of A150T, The gene ASXL2 has a mutation status of Q958Ter, The gene CAPN14 has a mutation status of Y182Ter, The gene CRIM1 has a mutation status of D1000E, The gene EML4 has a mutation status of K406R, The gene PTCD3 has a mutation status of I375N, The gene SLC9A2 has a mutation status of I376T, The gene SH3RF3 has a mutation status of N537I, The gene TNFAIP6 has a mutation status of H276_L277delinsQ, The gene NEB has a mutation status of E3803D, The gene SCN1A has a mutation status of I1228T, The gene LRP2 has a mutation status of G2802V, The gene LRP2 has a mutation status of L869I, The gene TTN has a mutation status of D2655N, The gene C2orf80 has a mutation status of K170N, The gene PLCB1 has a mutation status of D206Y, The gene RALGAPA2 has a mutation status of L1357R, The gene SYNDIG1 has a mutation status of V242M, The gene SLC32A1 has a mutation status of A35V, The gene ADAMTS1 has a mutation status of S134R, The gene GART has a mutation status of C93I, The gene CABIN1 has a mutation status of F463C, The gene MYO18B has a mutation status of K1825R, The gene SBF1 has a mutation status of R567H, The gene GRM7 has a mutation status of P40K, The gene SSUH2 has a mutation status of E52G, The gene TATDN2 has a mutation status of E550K, The gene GALNT15 has a mutation status of W487C, The gene SATB1 has a mutation status of V511M, The gene LSAMP has a mutation status of Q114H, The gene CASR has a mutation status of I235N, The gene TMCC1 has a mutation status of Q59H, The gene AADACL2 has a mutation status of L128M, The gene ARHGEF26 has a mutation status of E295D, The gene SLITRK3 has a mutation status of R777H, The gene SLITRK3 has a mutation status of A112E, The gene IDUA has a mutation status of P357A, The gene CRMP1 has a mutation status of I111T, The gene SLIT2 has a mutation status of A1247V, The gene DHX15 has a mutation status of E328Q, The gene UGT2B11 has a mutation status of G186R, The gene UGT2A2 has a mutation status of P291L, The gene GK2 has a mutation status of G320C, The gene ELF2 has a mutation status of M171K, The gene RNF150 has a mutation status of H97Q, The gene SPEF2 has a mutation status of P1448S, The gene GZMK has a mutation status of S34L, The gene GRIA1 has a mutation status of G905V, The gene NUP153 has a mutation status of D341F, The gene CDKAL1 has a mutation status of V157FfsTer17, The gene HLA-C has a mutation status of R132H, The gene USP49 has a mutation status of R225C, The gene CYB5R4 has a mutation status of F78Y, The gene ASF1A has a mutation status of F28SfsTer30, The gene ADGB has a mutation status of G164R, The gene THBS2 has a mutation status of T507I, The gene ZMIZ2 has a mutation status of L550Q, The gene TNS3 has a mutation status of Q1166Ter, The gene PKD1L1 has a mutation status of P272S, The gene EGFR has a mutation status of E746_A750del, The gene SEMA3D has a mutation status of A150E, The gene ELAPOR2 has a mutation status of Q43H, The gene ZSCAN25 has a mutation status of A100T, The gene RELN has a mutation status of H3447D, The gene RELN has a mutation status of S1773Ter, The gene LAMB1 has a mutation status of R255S, The gene ASB15 has a mutation status of R547SfsTer10, The gene PODXL has a mutation status of D373E, The gene ZNF777 has a mutation status of R720W, The gene GBX1 has a mutation status of A361P, The gene SOX7 has a mutation status of L103M, The gene DLC1 has a mutation status of Q917H, The gene UNC5D has a mutation status of A665P, The gene PXDNL has a mutation status of T837N, The gene ZFHX4 has a mutation status of P595RfsTer38, The gene LY6L has a mutation status of L138F, The gene MROH1 has a mutation status of Q705Ter, The gene RUSC2 has a mutation status of S987_I988del, The gene APBA1 has a mutation status of Q394H, The gene ROR2 has a mutation status of F739L, The gene PTCH1 has a mutation status of T314N, The gene TMOD1 has a mutation status of L254M, The gene TLR4 has a mutation status of D60V, The gene NOTCH1 has a mutation status of R1991C, The gene MT-ND4L has a mutation status of C69W, The gene MT-ND4 has a mutation status of N390S, The gene MT-ND4 has a mutation status of L445F, The gene MT-ND5 has a mutation status of A219V, The gene MT-ND5 has a mutation status of P265S, The gene NLGN4X has a mutation status of P111H, The gene PIGA has a mutation status of C356KfsTer10, The gene SUPT20HL1 has a mutation status of Q649Ter, The gene ARX has a mutation status of P38S, The gene MAGEB6B has a mutation status of S38F, The gene MAGEB1 has a mutation status of P66L, The gene XK has a mutation status of E117D, The gene CCNB3 has a mutation status of H1336R, The gene UBQLN2 has a mutation status of A469S, The gene NXF3 has a mutation status of R76W, The gene WDR44 has a mutation status of P142L, The gene WDR44 has a mutation status of S143F, The gene CT47C1 has a mutation status of K293N, The gene TENM1 has a mutation status of Y2238N, The gene TENM1 has a mutation status of Y1707Ter, The gene MAMLD1 has a mutation status of I166N, The gene GABRA3 has a mutation status of S442I, The gene IL9R has a mutation status of A195S	LUAD
The gene AGRN has a mutation status of P32S, The gene TTC34 has a mutation status of A493G, The gene ACTRT2 has a mutation status of S139Ter, The gene C1orf127 has a mutation status of L239P, The gene MFN2 has a mutation status of R259C, The gene EPHA2 has a mutation status of V554F, The gene ECE1 has a mutation status of A336P, The gene AHDC1 has a mutation status of V712G, The gene MTF1 has a mutation status of E429D, The gene IL23R has a mutation status of G599W, The gene PLPPR5 has a mutation status of Y205N, The gene NTNG1 has a mutation status of D255G, The gene WNT2B has a mutation status of K327R, The gene TCHHL1 has a mutation status of R156G, The gene GBA1 has a mutation status of E9D, The gene SYT11 has a mutation status of R251C, The gene MEF2D has a mutation status of S180P, The gene ARHGEF11 has a mutation status of P597H, The gene SPTA1 has a mutation status of G1402W, The gene SPTA1 has a mutation status of A221D, The gene CASQ1 has a mutation status of D379GfsTer41, The gene PRRC2C has a mutation status of Q2800K, The gene KIAA1614 has a mutation status of W1180LfsTer43, The gene CACNA1E has a mutation status of Y2172Ter, The gene CFH has a mutation status of Y1205Ter, The gene CRB1 has a mutation status of D168H, The gene PLEKHA6 has a mutation status of C996Ter, The gene OBSCN has a mutation status of A6826P, The gene GALNT2 has a mutation status of D134GfsTer6, The gene RYR2 has a mutation status of I1268K, The gene ZNF496 has a mutation status of S388F, The gene DIP2C has a mutation status of E961K, The gene RASGEF1A has a mutation status of V386F, The gene MAPK8 has a mutation status of I157V, The gene WDFY4 has a mutation status of P3121L, The gene C10orf71 has a mutation status of N405K, The gene ERCC6 has a mutation status of G917_G918insL, The gene NRG3 has a mutation status of D608E, The gene PLCE1 has a mutation status of Q854K, The gene CYP2C9 has a mutation status of Q340K, The gene PSD has a mutation status of P168T, The gene AFAP1L2 has a mutation status of R535Ter, The gene PNLIP has a mutation status of S405Ter, The gene DHX32 has a mutation status of I146V, The gene CFAP46 has a mutation status of V2593M, The gene TUBGCP2 has a mutation status of D220Y, The gene CALY has a mutation status of Q217H, The gene MUC5AC has a mutation status of C20Ter, The gene MUC5AC has a mutation status of V307A, The gene MUC5AC has a mutation status of Y1244Ter, The gene MUC5B has a mutation status of L1772F, The gene PRR33 has a mutation status of V12G, The gene OR52B6 has a mutation status of H200D, The gene DENND2B has a mutation status of K724E, The gene USP47 has a mutation status of R229EfsTer4, The gene ABCC8 has a mutation status of L175M, The gene OTOG has a mutation status of P910L, The gene SLC6A5 has a mutation status of L658F, The gene NAT10 has a mutation status of N738S, The gene OR4A16 has a mutation status of D20Y, The gene OR4C6 has a mutation status of T190N, The gene OR5W2 has a mutation status of M45I, The gene OR8U3 has a mutation status of H235Q, The gene TAF6L has a mutation status of A591D, The gene ZNRD2 has a mutation status of Q116E, The gene PCNX3 has a mutation status of R769L, The gene ANO1 has a mutation status of Y30Ter, The gene HEPHL1 has a mutation status of F699Y, The gene KDM4E has a mutation status of E215G, The gene ARHGAP20 has a mutation status of S1163RfsTer17, The gene APOBEC1 has a mutation status of W235L, The gene PIK3C2G has a mutation status of L588F, The gene SLCO1B1 has a mutation status of K285E, The gene MUC19 has a mutation status of I6366K, The gene ADAMTS20 has a mutation status of D1203E, The gene ARID2 has a mutation status of Q1678L, The gene STAB2 has a mutation status of L1066I, The gene LATS2 has a mutation status of G310W, The gene PDX1 has a mutation status of E69Ter, The gene MYO16 has a mutation status of P1551H, The gene TTC6 has a mutation status of D1150H, The gene CEP128 has a mutation status of A624S, The gene ATG2B has a mutation status of P757S, The gene SETD3 has a mutation status of A461S, The gene KIF26A has a mutation status of S47R, The gene KIF26A has a mutation status of R48P, The gene KIF26A has a mutation status of R644QfsTer44, The gene KIF26A has a mutation status of R644G, The gene JAG2 has a mutation status of V131F, The gene SNRPN has a mutation status of P218Q, The gene DISP2 has a mutation status of L1014V, The gene UBR1 has a mutation status of S1075RfsTer4, The gene HCN4 has a mutation status of D329Y, The gene SCAPER has a mutation status of M476N, The gene TMC3 has a mutation status of G808E, The gene CAPN15 has a mutation status of P179T, The gene RHBDL1 has a mutation status of R218S, The gene BAIAP3 has a mutation status of H423Q, The gene BAIAP3 has a mutation status of S427R, The gene PTX4 has a mutation status of G311A, The gene DNAJA3 has a mutation status of G464A, The gene ABCC12 has a mutation status of G683R, The gene LPCAT2 has a mutation status of Q57H, The gene PHAF1 has a mutation status of W17Ter, The gene TANGO6 has a mutation status of D386N, The gene CBFA2T3 has a mutation status of S131P, The gene CHRNE has a mutation status of E432D, The gene TP53 has a mutation status of Q144Ter, The gene CFAP52 has a mutation status of N23D, The gene MYH1 has a mutation status of L1337_S1339delinsP, The gene ANKRD13B has a mutation status of P541T, The gene CCL3L3 has a mutation status of T30M, The gene ARHGAP23 has a mutation status of V136D, The gene SRCIN1 has a mutation status of E189Ter, The gene PGAP3 has a mutation status of G265A, The gene KRT12 has a mutation status of R414W, The gene HOXB4 has a mutation status of P86L, The gene ABCC3 has a mutation status of L1441F, The gene GAA has a mutation status of P161QfsTer15, The gene NDUFAF8 has a mutation status of C35G, The gene GATA6 has a mutation status of D404G, The gene LOXHD1 has a mutation status of R587Q, The gene WDR7 has a mutation status of K801E, The gene CDH20 has a mutation status of R89K, The gene ZNF516 has a mutation status of Q417H, The gene MIER2 has a mutation status of Y96Ter, The gene MED16 has a mutation status of P538S, The gene APC2 has a mutation status of R818A, The gene APC2 has a mutation status of T819S, The gene KLF16 has a mutation status of D215E, The gene LONP1 has a mutation status of W69R, The gene TYK2 has a mutation status of S350QfsTer30, The gene TYK2 has a mutation status of A349T, The gene SMARCA4 has a mutation status of E1310Ter, The gene DOCK6 has a mutation status of A1691G, The gene ZNF763 has a mutation status of V209F, The gene HOOK2 has a mutation status of E459D, The gene SCN1B has a mutation status of S95R, The gene SIPA1L3 has a mutation status of N1752D, The gene KCNK6 has a mutation status of V190G, The gene CAPN12 has a mutation status of E162V, The gene PRX has a mutation status of A330G, The gene MEGF8 has a mutation status of T183P, The gene ZNF229 has a mutation status of G764S, The gene NPAS1 has a mutation status of H396N, The gene SLC8A2 has a mutation status of G712V, The gene PRR12 has a mutation status of N2011T, The gene AP2A1 has a mutation status of Y268S, The gene IGLON5 has a mutation status of G177V, The gene CLDND2 has a mutation status of G88C, The gene ZNF671 has a mutation status of Y479H, The gene KIDINS220 has a mutation status of Q1249H, The gene RAD51AP2 has a mutation status of Q944H, The gene NCOA1 has a mutation status of T73I, The gene TCF23 has a mutation status of G69C, The gene C2orf16 has a mutation status of S4850F, The gene ABCG5 has a mutation status of A155T, The gene ABCG5 has a mutation status of A152E, The gene SOCS5 has a mutation status of S425F, The gene MSH6 has a mutation status of T1085N, The gene DYSF has a mutation status of P1037T, The gene REG1A has a mutation status of R44L, The gene GLI2 has a mutation status of M1389L, The gene RIF1 has a mutation status of P2294L, The gene TBR1 has a mutation status of S141R, The gene IFIH1 has a mutation status of A691G, The gene SCN2A has a mutation status of R524L, The gene TTC21B has a mutation status of A285S, The gene TTN has a mutation status of R22288L, The gene TTN has a mutation status of W18319C, The gene TTN has a mutation status of N8384Y, The gene TTN has a mutation status of S5198Y, The gene MAP2 has a mutation status of P524L, The gene RPE has a mutation status of R25G, The gene SLC4A3 has a mutation status of R107S, The gene FAM124B has a mutation status of P225S, The gene COL4A4 has a mutation status of G834W, The gene KIF1A has a mutation status of Y384Ter, The gene VPS16 has a mutation status of R505P, The gene APMAP has a mutation status of D254Y, The gene XKR7 has a mutation status of A78GfsTer380, The gene COMMD7 has a mutation status of L25M, The gene BPIFB1 has a mutation status of Q336K, The gene C20orf144 has a mutation status of L33P, The gene NCOA6 has a mutation status of A196T, The gene DLGAP4 has a mutation status of Y76C, The gene TGM2 has a mutation status of Q348L, The gene FAM83D has a mutation status of R160L, The gene ZNF217 has a mutation status of C674S, The gene DIDO1 has a mutation status of R1643P, The gene DIDO1 has a mutation status of G1641P, The gene PRPF6 has a mutation status of I491T, The gene RIPK4 has a mutation status of R317W, The gene COL18A1 has a mutation status of P845L, The gene GAB4 has a mutation status of A508D, The gene ARVCF has a mutation status of V416L, The gene BCR has a mutation status of Y644Ter, The gene KIAA1671 has a mutation status of P1356T, The gene SEZ6L has a mutation status of P101R, The gene TTC28 has a mutation status of K1471N, The gene ZNRF3 has a mutation status of E812Ter, The gene SLC35E4 has a mutation status of A59G, The gene DEPDC5 has a mutation status of P1434T, The gene BPIFC has a mutation status of L320I, The gene RAC2 has a mutation status of P140L, The gene MTMR14 has a mutation status of A508G, The gene ATG7 has a mutation status of Y51C, The gene ARPP21 has a mutation status of L84F, The gene CELSR3 has a mutation status of F1520_P1521delinsLT, The gene WDR6 has a mutation status of A881G, The gene CFAP44 has a mutation status of R692S, The gene SLC49A4 has a mutation status of S300A, The gene H1-8 has a mutation status of Q99H, The gene TRIM42 has a mutation status of S69P, The gene ERICH6 has a mutation status of P460T, The gene MLF1 has a mutation status of H22D, The gene KPNA4 has a mutation status of C191S, The gene KNG1 has a mutation status of G518S, The gene BOD1L1 has a mutation status of N2607Y, The gene LCORL has a mutation status of D1501G, The gene DCAF4L1 has a mutation status of W341C, The gene ATP8A1 has a mutation status of A827P, The gene KIT has a mutation status of S123Y, The gene ADGRL3 has a mutation status of E1276D, The gene ANKRD17 has a mutation status of H71Y, The gene ANKRD17 has a mutation status of Q70Ter, The gene SEC24B has a mutation status of Y680C, The gene JADE1 has a mutation status of Y530Ter, The gene TBC1D9 has a mutation status of G1081A, The gene INPP4B has a mutation status of W521L, The gene NR3C2 has a mutation status of A301V, The gene GRIA2 has a mutation status of Y388Ter, The gene ADAM29 has a mutation status of H28L, The gene STOX2 has a mutation status of K635N, The gene H3Y1 has a mutation status of A89T, The gene NADK2 has a mutation status of I126del, The gene PRKAA1 has a mutation status of S494W, The gene MAST4 has a mutation status of A2407T, The gene AGGF1 has a mutation status of G248S, The gene ARSB has a mutation status of Y210F, The gene APC has a mutation status of A1107SfsTer12, The gene DMXL1 has a mutation status of L2888F, The gene PRDM6 has a mutation status of Q571K, The gene FBN2 has a mutation status of C1323S, The gene PITX1 has a mutation status of L55R, The gene PITX1 has a mutation status of T53S, The gene PCDHGA7 has a mutation status of W27C, The gene PCDHGA10 has a mutation status of A635V, The gene PWWP2A has a mutation status of A104P, The gene EIF4E1B has a mutation status of V140G, The gene TRIM41 has a mutation status of D223Y, The gene FOXF2 has a mutation status of G236A, The gene TXNDC5 has a mutation status of Q96E, The gene SLC35B3 has a mutation status of V65F, The gene DCDC2 has a mutation status of P305T, The gene H3C11 has a mutation status of R54C, The gene H3C11 has a mutation status of R41P, The gene HLA-A has a mutation status of I121R, The gene HLA-A has a mutation status of K292E, The gene BRD2 has a mutation status of A49C, The gene TBC1D22B has a mutation status of L442I, The gene SLC29A1 has a mutation status of L410P, The gene ADGRB3 has a mutation status of L234V, The gene BEND3 has a mutation status of G287V, The gene GJA1 has a mutation status of L347P, The gene MOXD1 has a mutation status of E374D, The gene DACT2 has a mutation status of Y719C, The gene ETV1 has a mutation status of R37S, The gene TRGV5 has a mutation status of I104NfsTer2, The gene SUGCT has a mutation status of A67T, The gene HECW1 has a mutation status of G665V, The gene AUTS2 has a mutation status of V1014M, The gene PCLO has a mutation status of E1936D, The gene SEMA3D has a mutation status of S709T, The gene TECPR1 has a mutation status of V226S, The gene GPC2 has a mutation status of R378L, The gene RELN has a mutation status of G53S, The gene TMEM229A has a mutation status of V150G, The gene TRBV14 has a mutation status of F26S, The gene SLC4A2 has a mutation status of Q400E, The gene ACTR3B has a mutation status of I358AfsTer42, The gene ERLIN2 has a mutation status of D87N, The gene ERLIN2 has a mutation status of E90K, The gene PXDNL has a mutation status of C869F, The gene CA3 has a mutation status of D161N, The gene DCSTAMP has a mutation status of V436F, The gene KIAA2026 has a mutation status of G462S, The gene MPDZ has a mutation status of R1150K, The gene SHB has a mutation status of L395QfsTer54, The gene TRPM6 has a mutation status of T1311I, The gene LHX6 has a mutation status of Q293H, The gene DENND1A has a mutation status of Q589PfsTer41, The gene ST6GALNAC6 has a mutation status of C10G, The gene SARDH has a mutation status of R691Ter, The gene KCNT1 has a mutation status of S762_S763delinsRP, The gene ABCA2 has a mutation status of E536G, The gene RAI2 has a mutation status of P415H, The gene MAP3K15 has a mutation status of A860D, The gene DCAF8L2 has a mutation status of C283R, The gene IQSEC2 has a mutation status of R1122S, The gene SLC25A5 has a mutation status of T221R, The gene PLXNA3 has a mutation status of T1024P, The gene PLXNA3 has a mutation status of T1026P, The gene VBP1 has a mutation status of K153M, The gene DDX3Y has a mutation status of V319L	LUAD
The gene TTLL10 has a mutation status of H10L, The gene NPHP4 has a mutation status of E1376K, The gene PADI4 has a mutation status of W296C, The gene AKR7A3 has a mutation status of F194L, The gene E2F2 has a mutation status of I169M, The gene HMGCL has a mutation status of M4T, The gene SF3A3 has a mutation status of Q283H, The gene C8A has a mutation status of S449A, The gene CACHD1 has a mutation status of A1272CfsTer47, The gene RAVER2 has a mutation status of A561T, The gene SYDE2 has a mutation status of N489S, The gene AGL has a mutation status of T221I, The gene RNPC3 has a mutation status of L289W, The gene LCE7A has a mutation status of Q73R, The gene NES has a mutation status of E996K, The gene PRCC has a mutation status of S222C, The gene IGSF9 has a mutation status of Q103E, The gene PPP1R12B has a mutation status of E453Ter, The gene IKBKE has a mutation status of R706W, The gene PTPN14 has a mutation status of R163G, The gene SPATA17 has a mutation status of R275T, The gene NMT2 has a mutation status of D186N, The gene MYO3A has a mutation status of G44D, The gene ZNF239 has a mutation status of G7V, The gene ALOX5 has a mutation status of E173K, The gene EGR2 has a mutation status of P252S, The gene CCAR1 has a mutation status of Q171E, The gene CRTAC1 has a mutation status of E383Q, The gene CTBP2 has a mutation status of T797N, The gene UTF1 has a mutation status of E127Q, The gene IFITM1 has a mutation status of F100L, The gene MUC5AC has a mutation status of L1260P, The gene TRIM5 has a mutation status of R124H, The gene IRAG1 has a mutation status of E534K, The gene TNKS1BP1 has a mutation status of S1503F, The gene SLC15A3 has a mutation status of D193H, The gene SPTBN2 has a mutation status of R1006Q, The gene KRTAP5-7 has a mutation status of C146Y, The gene COA4 has a mutation status of D26H, The gene UVRAG has a mutation status of R695S, The gene GAB2 has a mutation status of E417Q, The gene CREBZF has a mutation status of L102V, The gene PCSK7 has a mutation status of Q393H, The gene SMIM35 has a mutation status of M1?, The gene VPS11 has a mutation status of D789Y, The gene DDX25 has a mutation status of D482N, The gene IGSF9B has a mutation status of S633C, The gene DYRK4 has a mutation status of R386L, The gene AKAP3 has a mutation status of E570Q, The gene PLEKHA5 has a mutation status of R600T, The gene MUC19 has a mutation status of R4331G, The gene MUC19 has a mutation status of Ter5837_S5838delinsCC, The gene ERBB3 has a mutation status of E952Q, The gene XPOT has a mutation status of I315V, The gene TMEM263 has a mutation status of A71S, The gene FZD10 has a mutation status of V386M, The gene SPRY2 has a mutation status of D232H, The gene MCF2L has a mutation status of S19F, The gene F10 has a mutation status of M336T, The gene KLHL33 has a mutation status of E53G, The gene AKAP6 has a mutation status of A528V, The gene SRP54 has a mutation status of D190H, The gene PSMA6 has a mutation status of E19K, The gene FERMT2 has a mutation status of S371F, The gene SYNE2 has a mutation status of L6463F, The gene VIPAS39 has a mutation status of N439EfsTer5, The gene GPR65 has a mutation status of V236F, The gene EFCAB11 has a mutation status of D140N, The gene PACS2 has a mutation status of L360P, The gene MAGEL2 has a mutation status of R295T, The gene MAGEL2 has a mutation status of P225A, The gene HERC2 has a mutation status of L3391Q, The gene BUB1B has a mutation status of A46G, The gene DUOX1 has a mutation status of Q451P, The gene DENND4A has a mutation status of I1481M, The gene HCN4 has a mutation status of I1086M, The gene PERCC1 has a mutation status of G140R, The gene UBN1 has a mutation status of A276V, The gene KLHL36 has a mutation status of A362T, The gene TP53 has a mutation status of R175H, The gene HS3ST3B1 has a mutation status of G107A, The gene RAB34 has a mutation status of G124E, The gene STAT5B has a mutation status of E509K, The gene HSF5 has a mutation status of G34S, The gene HEATR6 has a mutation status of R778T, The gene CSHL1 has a mutation status of E160Ter, The gene SKOR2 has a mutation status of P545S, The gene CDH20 has a mutation status of E688Q, The gene ZCCHC2 has a mutation status of S89W, The gene CDH7 has a mutation status of P726A, The gene ATP9B has a mutation status of E675Q, The gene CACTIN has a mutation status of Q591H, The gene MUC16 has a mutation status of W9392S, The gene ZNF441 has a mutation status of H50D, The gene CPAMD8 has a mutation status of F583C, The gene ZNF730 has a mutation status of E455Q, The gene CAPNS1 has a mutation status of L246F, The gene ZNF585B has a mutation status of L677F, The gene LRFN1 has a mutation status of R487S, The gene TPRX1 has a mutation status of D397E, The gene SCAF1 has a mutation status of E871D, The gene KIR2DL4 has a mutation status of P186S, The gene SULT6B1 has a mutation status of D56N, The gene SOS1 has a mutation status of E906Q, The gene USP34 has a mutation status of S3332Ter, The gene USP34 has a mutation status of L3312V, The gene WDPCP has a mutation status of R728T, The gene TMEM131 has a mutation status of Q1312Ter, The gene INHBB has a mutation status of D311E, The gene TFCP2L1 has a mutation status of Q198H, The gene NMI has a mutation status of E240V, The gene TBR1 has a mutation status of S620W, The gene SCN9A has a mutation status of E937K, The gene LRP2 has a mutation status of E1239K, The gene CFAP210 has a mutation status of Q528P, The gene PHOSPHO2 has a mutation status of D10H, The gene HNRNPA3 has a mutation status of Q213H, The gene COL5A2 has a mutation status of R1283C, The gene STK17B has a mutation status of P344R, The gene ALS2 has a mutation status of E1557Q, The gene CRYGD has a mutation status of R169K, The gene ABCA12 has a mutation status of T913I, The gene ABCB6 has a mutation status of Y106C, The gene ARMC9 has a mutation status of A786PfsTer60, The gene NMUR1 has a mutation status of F100L, The gene RBM44 has a mutation status of S709Ter, The gene XRN2 has a mutation status of P148L, The gene NCOA6 has a mutation status of S2038C, The gene MMP24 has a mutation status of M1?, The gene MMP24 has a mutation status of S4L, The gene PHF20 has a mutation status of E858Q, The gene ELMO2 has a mutation status of F555L, The gene PREX1 has a mutation status of N643K, The gene CSE1L has a mutation status of M352I, The gene CSE1L has a mutation status of E353delinsVDLYTer, The gene RTF2 has a mutation status of M249I, The gene NCAM2 has a mutation status of E252K, The gene HLCS has a mutation status of Q65G, The gene DSCAM has a mutation status of R498Ter, The gene MX1 has a mutation status of R649Q, The gene COL18A1 has a mutation status of P992L, The gene P2RX6 has a mutation status of K208_F209del, The gene BCR has a mutation status of E1161D, The gene MN1 has a mutation status of A612T, The gene GAS2L1 has a mutation status of E123Q, The gene SEC14L6 has a mutation status of G221E, The gene SMTN has a mutation status of E124Q, The gene FOXRED2 has a mutation status of S4C, The gene GCAT has a mutation status of S261C, The gene LMCD1 has a mutation status of K139R, The gene RAB5A has a mutation status of R197T, The gene ZNF385D has a mutation status of S217L, The gene WDR6 has a mutation status of H567L, The gene DNAH1 has a mutation status of A3155T, The gene UPK1B has a mutation status of W141Ter, The gene RASA2 has a mutation status of T634R, The gene TIPARP has a mutation status of M303I, The gene PSMD2 has a mutation status of G155C, The gene MELTF has a mutation status of E316Q, The gene UGDH has a mutation status of E416Q, The gene BEND4 has a mutation status of E272Ter, The gene UGT2B7 has a mutation status of Q330Ter, The gene CCDC158 has a mutation status of D163N, The gene PDE5A has a mutation status of I813T, The gene FGG has a mutation status of D346H, The gene ZSWIM6 has a mutation status of D1071N, The gene NSA2 has a mutation status of L90V, The gene PCDHA2 has a mutation status of E558K, The gene LSM11 has a mutation status of R23W, The gene TENM2 has a mutation status of L1883M, The gene GMCL2 has a mutation status of V468AfsTer15, The gene H4C4 has a mutation status of D69H, The gene BTN2A2 has a mutation status of T180A, The gene HLA-F has a mutation status of D60H, The gene MUC22 has a mutation status of T273E, The gene HCG22 has a mutation status of S186F, The gene HLA-DOA has a mutation status of F163L, The gene SRPK1 has a mutation status of E57Q, The gene TRERF1 has a mutation status of V28A, The gene CUL9 has a mutation status of E513Q, The gene PKHD1 has a mutation status of W365Ter, The gene FAM83B has a mutation status of I20V, The gene AK9 has a mutation status of E198Q, The gene TRAF3IP2 has a mutation status of Q561K, The gene SAMD3 has a mutation status of T487I, The gene SYNE1 has a mutation status of D4750H, The gene TULP4 has a mutation status of S676C, The gene SLC22A1 has a mutation status of L8V, The gene PACRG has a mutation status of T168I, The gene EIF3B has a mutation status of D171H, The gene ADCY1 has a mutation status of S149F, The gene TNS3 has a mutation status of S944C, The gene ABCA13 has a mutation status of A703G, The gene AUTS2 has a mutation status of S1233C, The gene MAGI2 has a mutation status of R109S, The gene PCLO has a mutation status of Q442Ter, The gene CLDN12 has a mutation status of L138M, The gene VPS50 has a mutation status of M625I, The gene NPTX2 has a mutation status of R103P, The gene ZAN has a mutation status of I1243T, The gene MUC17 has a mutation status of P753S, The gene PIP has a mutation status of L143I, The gene GALNT11 has a mutation status of D275H, The gene KMT2C has a mutation status of Q2054E, The gene VIPR2 has a mutation status of L298F, The gene XKR5 has a mutation status of S368R, The gene TUSC3 has a mutation status of Q94K, The gene PAG1 has a mutation status of E278Q, The gene MTDH has a mutation status of Q372E, The gene VPS13B has a mutation status of D2772H, The gene SPAG1 has a mutation status of A368G, The gene YWHAZ has a mutation status of S45L, The gene UBR5 has a mutation status of H1585N, The gene ZNF623 has a mutation status of R352Q, The gene IQANK1 has a mutation status of W467R, The gene PLEC has a mutation status of Q512Ter, The gene SMARCA2 has a mutation status of R424K, The gene BNC2 has a mutation status of V559L, The gene TOPORS has a mutation status of L184V, The gene UBAP1 has a mutation status of I263M, The gene CD72 has a mutation status of T331S, The gene GRHPR has a mutation status of K134N, The gene RASEF has a mutation status of S25L, The gene SLC28A3 has a mutation status of S466L, The gene CNTRL has a mutation status of L1943R, The gene NR6A1 has a mutation status of A285S, The gene PRDM12 has a mutation status of A344T, The gene SEC16A has a mutation status of R229S, The gene TRAF2 has a mutation status of K481N, The gene CYBB has a mutation status of K508N, The gene JADE3 has a mutation status of E42Q, The gene HEPH has a mutation status of P395R, The gene ABCB7 has a mutation status of E731G, The gene TRPC5 has a mutation status of E421K, The gene LUZP4 has a mutation status of H205Y, The gene TTLL10 has a mutation status of H10L, The gene NPHP4 has a mutation status of E1376K, The gene PADI4 has a mutation status of W296C, The gene AKR7A3 has a mutation status of F194L, The gene E2F2 has a mutation status of I169M, The gene HMGCL has a mutation status of M4T, The gene SF3A3 has a mutation status of Q283H, The gene CDCP2 has a mutation status of T157S, The gene C8A has a mutation status of S449A, The gene RAVER2 has a mutation status of A561T, The gene MIER1 has a mutation status of D319H, The gene DEPDC1 has a mutation status of E363Q, The gene SYDE2 has a mutation status of N489S, The gene HFM1 has a mutation status of S593P, The gene AGL has a mutation status of T221I, The gene RNPC3 has a mutation status of L289W, The gene WNT2B has a mutation status of S26L, The gene TCHH has a mutation status of R615GfsTer6, The gene PKLR has a mutation status of E106K, The gene SEMA4A has a mutation status of G441E, The gene NES has a mutation status of E996K, The gene PRCC has a mutation status of S222C, The gene FCRL5 has a mutation status of G608E, The gene FCRL1 has a mutation status of E116K, The gene IGSF9 has a mutation status of Q103E, The gene HMCN1 has a mutation status of E4445Ter, The gene IGFN1 has a mutation status of M1630KfsTer5, The gene TIMM17A has a mutation status of K86E, The gene PPP1R12B has a mutation status of E453Ter, The gene CNTN2 has a mutation status of R506P, The gene IKBKE has a mutation status of R706W, The gene PTPN14 has a mutation status of R163G, The gene SPATA17 has a mutation status of R275T, The gene CAPN2 has a mutation status of S619C, The gene ACBD3 has a mutation status of E8K, The gene PGBD2 has a mutation status of E264Q, The gene PRKCQ has a mutation status of E352K, The gene PRKCQ has a mutation status of P341L, The gene ITIH2 has a mutation status of E595K, The gene NMT2 has a mutation status of D186N, The gene MLLT10 has a mutation status of Q981E, The gene MYO3A has a mutation status of G44D, The gene CSGALNACT2 has a mutation status of E50G, The gene ZNF239 has a mutation status of G7V, The gene ALOX5 has a mutation status of E173K, The gene JMJD1C has a mutation status of A90S, The gene SIRT1 has a mutation status of T177I, The gene CCAR1 has a mutation status of Q171E, The gene DDX21 has a mutation status of E446Q, The gene CRTAC1 has a mutation status of E383Q, The gene FGFR2 has a mutation status of G364E, The gene CTBP2 has a mutation status of T797N, The gene MKI67 has a mutation status of Q1497L, The gene UTF1 has a mutation status of E127Q, The gene IFITM1 has a mutation status of F100L, The gene MUC5B has a mutation status of I4642V, The gene TRIM5 has a mutation status of R124H, The gene OR56B2P has a mutation status of N57K, The gene OR52L1 has a mutation status of A215S, The gene IRAG1 has a mutation status of E534K, The gene TP53I11 has a mutation status of P102L, The gene NUP160 has a mutation status of L1287V, The gene FOLH1 has a mutation status of N51K, The gene OR5G3 has a mutation status of L32V, The gene TNKS1BP1 has a mutation status of S1503F, The gene SLC15A3 has a mutation status of D193H, The gene KCNK4 has a mutation status of A230V, The gene SPTBN2 has a mutation status of R1006Q, The gene CORO1B has a mutation status of A385V, The gene KRTAP5-7 has a mutation status of C146Y, The gene COA4 has a mutation status of D26H, The gene UVRAG has a mutation status of R695S, The gene GAB2 has a mutation status of E417Q, The gene CREBZF has a mutation status of L102V, The gene PCSK7 has a mutation status of Q393H, The gene VPS11 has a mutation status of D789Y, The gene PANX3 has a mutation status of S83A, The gene DDX25 has a mutation status of D482N, The gene IGSF9B has a mutation status of S633C, The gene GLB1L2 has a mutation status of E103Ter, The gene DCP1B has a mutation status of E540Ter, The gene DYRK4 has a mutation status of R386L, The gene AKAP3 has a mutation status of E570Q, The gene KCNA5 has a mutation status of F352L, The gene C1S has a mutation status of D222Y, The gene PLEKHA5 has a mutation status of R600T, The gene ANO6 has a mutation status of R208K, The gene ERBB3 has a mutation status of E952Q, The gene ZBTB39 has a mutation status of E534V, The gene GLI1 has a mutation status of I110M, The gene XPOT has a mutation status of I315V, The gene MYRFL has a mutation status of E478K, The gene LUM has a mutation status of L139V, The gene APPL2 has a mutation status of A387V, The gene TMEM263 has a mutation status of A71S, The gene FZD10 has a mutation status of V386M, The gene DDX51 has a mutation status of Y221N, The gene PCDH8 has a mutation status of T703N, The gene SPRY2 has a mutation status of D232H, The gene SLC15A1 has a mutation status of Q324H, The gene MCF2L has a mutation status of S19F, The gene F10 has a mutation status of M336T, The gene ADPRHL1 has a mutation status of R1245I, The gene MYH6 has a mutation status of Y835N, The gene AKAP6 has a mutation status of A528V, The gene SRP54 has a mutation status of D190H, The gene PSMA6 has a mutation status of E19K, The gene FERMT2 has a mutation status of S371F, The gene KIAA0586 has a mutation status of S286T, The gene SYNE2 has a mutation status of L6463F, The gene SPTB has a mutation status of D81N, The gene FLVCR2 has a mutation status of I383_L386delinsM, The gene VIPAS39 has a mutation status of N439EfsTer5, The gene GPR65 has a mutation status of V236F, The gene EFCAB11 has a mutation status of D140N, The gene CCDC88C has a mutation status of E167Q, The gene DIO3 has a mutation status of L32Q, The gene PACS2 has a mutation status of L360P, The gene IGHV4-59 has a mutation status of E35Q, The gene MAGEL2 has a mutation status of R295T, The gene MAGEL2 has a mutation status of P225A, The gene OCA2 has a mutation status of L734Q, The gene HERC2 has a mutation status of L3391Q, The gene BUB1B has a mutation status of A46G, The gene DUOX1 has a mutation status of Q451P, The gene MINDY2 has a mutation status of R445W, The gene SLC24A1 has a mutation status of P284S, The gene DENND4A has a mutation status of I1481M, The gene HCN4 has a mutation status of I1086M, The gene CYP11A1 has a mutation status of L288F, The gene ADAMTSL3 has a mutation status of G1338R, The gene ANPEP has a mutation status of E389D, The gene ADAMTS17 has a mutation status of R60G, The gene UBN1 has a mutation status of A276V, The gene HAPSTR1 has a mutation status of A67D, The gene DNAH3 has a mutation status of F604L, The gene UQCRC2 has a mutation status of V292F, The gene APOBR has a mutation status of E46Ter, The gene RUSF1 has a mutation status of D139N, The gene CDH8 has a mutation status of G170V, The gene PMFBP1 has a mutation status of E855Q, The gene PMFBP1 has a mutation status of G204E, The gene GAN has a mutation status of L125F, The gene KLHL36 has a mutation status of A362T, The gene ZNF469 has a mutation status of A2512T, The gene ALOX15 has a mutation status of Q125H, The gene TP53 has a mutation status of R175H, The gene DNAH2 has a mutation status of E4369Q, The gene MYH3 has a mutation status of N898H, The gene DNAH9 has a mutation status of S208P, The gene HS3ST3B1 has a mutation status of G107A, The gene TEKT3 has a mutation status of I409S, The gene RAB34 has a mutation status of G124E, The gene NEK8 has a mutation status of I252M, The gene NF1 has a mutation status of A502V, The gene RAPGEFL1 has a mutation status of E359Ter, The gene STAT5B has a mutation status of E509K, The gene SLC4A1 has a mutation status of S106G, The gene HSF5 has a mutation status of G34S, The gene HEATR6 has a mutation status of R778T, The gene ACE has a mutation status of S824W, The gene CSHL1 has a mutation status of E160Ter, The gene MGAT5B has a mutation status of E479del, The gene L3MBTL4 has a mutation status of E551D, The gene MAPRE2 has a mutation status of S39Y, The gene ELOA2 has a mutation status of G326E, The gene SKOR2 has a mutation status of P545S, The gene SMAD4 has a mutation status of D355N, The gene CDH20 has a mutation status of E688Q, The gene ZCCHC2 has a mutation status of S89W, The gene CDH7 has a mutation status of P726A, The gene ATP9B has a mutation status of E675Q, The gene MUC16 has a mutation status of T13896S, The gene ZNF441 has a mutation status of H50D, The gene CPAMD8 has a mutation status of F583C, The gene CAPNS1 has a mutation status of L246F, The gene ZNF382 has a mutation status of I179T, The gene ZNF850 has a mutation status of G697C, The gene ZNF829 has a mutation status of G292D, The gene ZNF585B has a mutation status of L677F, The gene LRFN1 has a mutation status of R487S, The gene CBLC has a mutation status of S43L, The gene TPRX1 has a mutation status of D397E, The gene SCAF1 has a mutation status of E871D, The gene KIR2DL4 has a mutation status of P186S, The gene ZNF8 has a mutation status of C472Y, The gene SULT6B1 has a mutation status of D56N, The gene SOS1 has a mutation status of E906Q, The gene MTA3 has a mutation status of K543N, The gene ABCG5 has a mutation status of E452D, The gene MSH6 has a mutation status of S79L, The gene USP34 has a mutation status of S3332Ter, The gene USP34 has a mutation status of L3312V, The gene WDPCP has a mutation status of R728T, The gene UGP2 has a mutation status of E68D, The gene TMEM131 has a mutation status of Q1312Ter, The gene GCC2 has a mutation status of E250Q, The gene INHBB has a mutation status of D311E, The gene TFCP2L1 has a mutation status of Q198H, The gene WDR33 has a mutation status of R828K, The gene ARHGEF4 has a mutation status of G598V, The gene GPR39 has a mutation status of C108W, The gene NMI has a mutation status of E240V, The gene TBR1 has a mutation status of S620W, The gene SCN9A has a mutation status of E937K, The gene LRP2 has a mutation status of E1239K, The gene CFAP210 has a mutation status of Q528P, The gene PHOSPHO2 has a mutation status of D10H, The gene HNRNPA3 has a mutation status of Q213H, The gene TTN has a mutation status of E9882K, The gene COL5A2 has a mutation status of R1283C, The gene STK17B has a mutation status of P344R, The gene ALS2 has a mutation status of E1557Q, The gene BMPR2 has a mutation status of T578A, The gene CRYGD has a mutation status of R169K, The gene ABCA12 has a mutation status of T913I, The gene ABCB6 has a mutation status of Y106C, The gene ARMC9 has a mutation status of A786PfsTer60, The gene NMUR1 has a mutation status of F100L, The gene DGKD has a mutation status of D97H, The gene RBM44 has a mutation status of S709Ter, The gene ESF1 has a mutation status of A500G, The gene DTD1 has a mutation status of D202Y, The gene XRN2 has a mutation status of P148L, The gene NCOA6 has a mutation status of S2038C, The gene PHF20 has a mutation status of E858Q, The gene PLCG1 has a mutation status of E822D, The gene TOMM34 has a mutation status of E18Q, The gene CDH22 has a mutation status of V230A, The gene ELMO2 has a mutation status of F555L, The gene PREX1 has a mutation status of N643K, The gene RIPOR3 has a mutation status of V2M, The gene RTF2 has a mutation status of M249I, The gene NRIP1 has a mutation status of T970N, The gene CXADR has a mutation status of Q69E, The gene NCAM2 has a mutation status of E252K, The gene DSCAM has a mutation status of R498Ter, The gene MX1 has a mutation status of R649Q, The gene PRMT2 has a mutation status of A229V, The gene P2RX6 has a mutation status of K208_F209del, The gene BCR has a mutation status of E1161D, The gene MN1 has a mutation status of A612T, The gene GAS2L1 has a mutation status of E123Q, The gene SEC14L6 has a mutation status of G221E, The gene SMTN has a mutation status of E124Q, The gene FOXRED2 has a mutation status of S4C, The gene GCAT has a mutation status of S261C, The gene TNRC6B has a mutation status of L1254V, The gene KIAA0930 has a mutation status of M230L, The gene PLXNB2 has a mutation status of E1269GfsTer28, The gene LMCD1 has a mutation status of K139R, The gene MTMR14 has a mutation status of N218I, The gene RAB5A has a mutation status of R197T, The gene ZNF385D has a mutation status of S217L, The gene LARS2 has a mutation status of C467WfsTer58, The gene ALS2CL has a mutation status of G371E, The gene WDR6 has a mutation status of H567L, The gene UBA7 has a mutation status of L917V, The gene UPK1B has a mutation status of W141Ter, The gene PRR20G has a mutation status of L176F, The gene COPG1 has a mutation status of E100Q, The gene COL6A5 has a mutation status of G738R, The gene CPNE4 has a mutation status of D187N, The gene CLSTN2 has a mutation status of E162Q, The gene RASA2 has a mutation status of T634R, The gene GPR171 has a mutation status of K169R, The gene TIPARP has a mutation status of M303I, The gene TNIK has a mutation status of S77F, The gene PSMD2 has a mutation status of G155C, The gene MUC4 has a mutation status of S4181D, The gene MELTF has a mutation status of E316Q, The gene MYL5 has a mutation status of E140K, The gene PROM1 has a mutation status of Q755K, The gene UGDH has a mutation status of E416Q, The gene BEND4 has a mutation status of E272Ter, The gene GABRA4 has a mutation status of R466G, The gene UGT2B7 has a mutation status of Q330Ter, The gene ENAM has a mutation status of R373C, The gene GRSF1 has a mutation status of D148V, The gene CCDC158 has a mutation status of D163N, The gene BMP2K has a mutation status of E233V, The gene PTPN13 has a mutation status of P1971L, The gene AFF1 has a mutation status of K980T, The gene MCUB has a mutation status of W7Ter, The gene PDE5A has a mutation status of I813T, The gene FGG has a mutation status of D346H, The gene TKTL2 has a mutation status of P67S, The gene SCRG1 has a mutation status of E66K, The gene FAT1 has a mutation status of G1604E, The gene IRX1 has a mutation status of D264N, The gene SEMA5A has a mutation status of Y1060N, The gene CDH18 has a mutation status of K52Q, The gene PDZD2 has a mutation status of Q2579E, The gene ZSWIM6 has a mutation status of D1071N, The gene NSA2 has a mutation status of L90V, The gene THBS4 has a mutation status of T447A, The gene ADGRV1 has a mutation status of R1142K, The gene CEP120 has a mutation status of T209I, The gene PRRC1 has a mutation status of F277GfsTer36, The gene PCDHA2 has a mutation status of E558K, The gene LSM11 has a mutation status of R23W, The gene TENM2 has a mutation status of L1883M, The gene GMCL2 has a mutation status of V468AfsTer15, The gene NRSN1 has a mutation status of M130T, The gene BTN2A2 has a mutation status of T180A, The gene HLA-F has a mutation status of D60H, The gene MUC22 has a mutation status of T273E, The gene HCG22 has a mutation status of S186F, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DOA has a mutation status of F163L, The gene SRPK1 has a mutation status of E57Q, The gene TRERF1 has a mutation status of V28A, The gene CUL9 has a mutation status of E513Q, The gene MEP1A has a mutation status of W567C, The gene PKHD1 has a mutation status of W365Ter, The gene KLHL31 has a mutation status of E201Ter, The gene FAM83B has a mutation status of I20V, The gene COL12A1 has a mutation status of S234C, The gene SLC35A1 has a mutation status of A30P, The gene CASP8AP2 has a mutation status of E1255G, The gene EPHA7 has a mutation status of R366T, The gene AK9 has a mutation status of E198Q, The gene TRAF3IP2 has a mutation status of Q561K, The gene SAMD3 has a mutation status of T487I, The gene IFNGR1 has a mutation status of D144N, The gene SYNE1 has a mutation status of E7841Ter, The gene SYNE1 has a mutation status of D4750H, The gene SYNE1 has a mutation status of Q3063L, The gene TULP4 has a mutation status of S676C, The gene SLC22A1 has a mutation status of L8V, The gene PACRG has a mutation status of T168I, The gene EIF3B has a mutation status of D171H, The gene ABCB5 has a mutation status of S1059T, The gene SP8 has a mutation status of A94_A99del, The gene MATCAP2 has a mutation status of S467C, The gene ADCY1 has a mutation status of S149F, The gene TNS3 has a mutation status of S944C, The gene ABCA13 has a mutation status of A703G, The gene IKZF1 has a mutation status of G106V, The gene AUTS2 has a mutation status of S1233C, The gene MAGI2 has a mutation status of R109S, The gene PCLO has a mutation status of G1764A, The gene PCLO has a mutation status of Q442Ter, The gene CLDN12 has a mutation status of L138M, The gene VPS50 has a mutation status of M625I, The gene TECPR1 has a mutation status of G796V, The gene NPTX2 has a mutation status of R103P, The gene ZAN has a mutation status of I1243T, The gene MUC17 has a mutation status of P753S, The gene SLC26A5 has a mutation status of A347P, The gene CPED1 has a mutation status of C697F, The gene AASS has a mutation status of G510E, The gene PIP has a mutation status of L143I, The gene GALNT11 has a mutation status of D275H, The gene KMT2C has a mutation status of Q2054E, The gene SHH has a mutation status of T336S, The gene XKR5 has a mutation status of S368R, The gene TUSC3 has a mutation status of Q94K, The gene XPO7 has a mutation status of E699Q, The gene NEFM has a mutation status of K638Q, The gene RP1 has a mutation status of P387Q, The gene CYP7B1 has a mutation status of Y469C, The gene PAG1 has a mutation status of E278Q, The gene MTDH has a mutation status of Q372E, The gene VPS13B has a mutation status of D2772H, The gene SPAG1 has a mutation status of A368G, The gene YWHAZ has a mutation status of S45L, The gene UBR5 has a mutation status of H1585N, The gene FZD6 has a mutation status of L176V, The gene ZNF623 has a mutation status of R352Q, The gene PLEC has a mutation status of Q512Ter, The gene VPS28 has a mutation status of Y36Ter, The gene SMARCA2 has a mutation status of R424K, The gene BNC2 has a mutation status of V559L, The gene TOPORS has a mutation status of L184V, The gene UBAP1 has a mutation status of I263M, The gene CD72 has a mutation status of T331S, The gene GRHPR has a mutation status of K134N, The gene RASEF has a mutation status of S25L, The gene SLC28A3 has a mutation status of S466L, The gene ZNF367 has a mutation status of R144P, The gene CNTRL has a mutation status of L1943R, The gene NR6A1 has a mutation status of A285S, The gene RAPGEF1 has a mutation status of P81S, The gene NACC2 has a mutation status of E281D, The gene SEC16A has a mutation status of R229S, The gene TRAF2 has a mutation status of K481N, The gene NOXA1 has a mutation status of R180GfsTer12, The gene MT-ND5 has a mutation status of G146S, The gene P2RY8 has a mutation status of L304V, The gene TLR7 has a mutation status of K478E, The gene CYBB has a mutation status of K508N, The gene JADE3 has a mutation status of E42Q, The gene HEPH has a mutation status of P395R, The gene MED12 has a mutation status of S1400F, The gene ERCC6L has a mutation status of R650T, The gene ABCB7 has a mutation status of E731G, The gene FGF16 has a mutation status of R63C, The gene ZNF711 has a mutation status of Q796H, The gene HTR2C has a mutation status of A286S, The gene LUZP4 has a mutation status of H205Y, The gene C1GALT1C1 has a mutation status of L2V	BRCA
The gene SPEN has a mutation status of E1965del, The gene KIAA0319L has a mutation status of T901S, The gene FOXO6 has a mutation status of E170K, The gene TTC22 has a mutation status of S276Ter, The gene ZNHIT6 has a mutation status of E46D, The gene CD101 has a mutation status of R376K, The gene PYDC5 has a mutation status of N34S, The gene HMCN1 has a mutation status of E5601K, The gene PROX1 has a mutation status of P728L, The gene OBSCN has a mutation status of A2212L, The gene RYR2 has a mutation status of R2401H, The gene CUBN has a mutation status of H2366N, The gene CDH23 has a mutation status of A356P, The gene HRAS has a mutation status of G12V, The gene MUC5AC has a mutation status of A5353K, The gene ANO3 has a mutation status of K928N, The gene OR5D18 has a mutation status of A275V, The gene C2CD3 has a mutation status of R2252K, The gene DSCAML1 has a mutation status of P1090L, The gene C2CD2L has a mutation status of D616N, The gene C2CD2L has a mutation status of E620K, The gene CACNA2D4 has a mutation status of V298L, The gene ALG10B has a mutation status of D218N, The gene MUC19 has a mutation status of Y4423S, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene MUC19 has a mutation status of W4893_I4894insTISWSDRDNW, The gene MUC19 has a mutation status of S6579D, The gene FAM186B has a mutation status of F616C, The gene WIF1 has a mutation status of A149E, The gene MYRFL has a mutation status of P659Q, The gene ATXN2 has a mutation status of E246K, The gene N4BP2L2 has a mutation status of R371I, The gene MYCBP2 has a mutation status of K3014N, The gene NALCN has a mutation status of R1053I, The gene APBA2 has a mutation status of A397V, The gene UNC13C has a mutation status of Q1582H, The gene LACTB has a mutation status of K511R, The gene ALPK3 has a mutation status of D211N, The gene AGBL1 has a mutation status of D1076H, The gene HEATR3 has a mutation status of A436V, The gene MYO1C has a mutation status of L181W, The gene MNT has a mutation status of A23V, The gene CLUH has a mutation status of I1250M, The gene SPNS3 has a mutation status of A276S, The gene POLR2A has a mutation status of E1152Q, The gene POLR2A has a mutation status of E1188Q, The gene POLR2A has a mutation status of D1223N, The gene TP53 has a mutation status of Y126Ter, The gene NTN1 has a mutation status of S67C, The gene RNF112 has a mutation status of E177K, The gene DHX8 has a mutation status of P811Q, The gene PIEZO2 has a mutation status of S2690Ter, The gene EPG5 has a mutation status of L361GfsTer12, The gene CCDC68 has a mutation status of E80Q, The gene ZNF414 has a mutation status of P313G, The gene COL5A3 has a mutation status of V1162I, The gene FCHO1 has a mutation status of D478N, The gene ZNF729 has a mutation status of C908S, The gene HAUS5 has a mutation status of A627S, The gene ZNF585A has a mutation status of R458G, The gene ZNF155 has a mutation status of F400L, The gene ZC3H4 has a mutation status of P990S, The gene RASIP1 has a mutation status of A951G, The gene PXDN has a mutation status of D1432H, The gene GDF7 has a mutation status of C414Ter, The gene CAD has a mutation status of Q646Ter, The gene CAD has a mutation status of V1357F, The gene FOSL2 has a mutation status of G205AfsTer53, The gene TET3 has a mutation status of R160T, The gene FHL2 has a mutation status of R242W, The gene GALNT5 has a mutation status of E564G, The gene XIRP2 has a mutation status of P456T, The gene FSIP2 has a mutation status of S3169P, The gene TMEM237 has a mutation status of R192H, The gene ZNF142 has a mutation status of E416K, The gene COL6A3 has a mutation status of G2344R, The gene MTERF4 has a mutation status of Q75PfsTer3, The gene BPIFA1 has a mutation status of G86D, The gene PCIF1 has a mutation status of A552G, The gene CDH22 has a mutation status of G712A, The gene DIDO1 has a mutation status of E140Q, The gene MCM3AP has a mutation status of C1561R, The gene C21orf58 has a mutation status of A222P, The gene IGLV3-32 has a mutation status of D70H, The gene EP300 has a mutation status of C1201Y, The gene ZBED4 has a mutation status of M1036L, The gene PANX2 has a mutation status of R464H, The gene CCDC66 has a mutation status of Q108Ter, The gene AMOTL2 has a mutation status of R547Ter, The gene SLITRK3 has a mutation status of T567N, The gene ATP13A5 has a mutation status of Q1212E, The gene MUC4 has a mutation status of A2782_H2797del, The gene CRACD has a mutation status of R517L, The gene CCDC158 has a mutation status of E509Q, The gene TBCK has a mutation status of S277Ter, The gene QRFPR has a mutation status of E397K, The gene OTUD4 has a mutation status of S1072EfsTer10, The gene OTUD4 has a mutation status of E1071SfsTer53, The gene TKTL2 has a mutation status of F170S, The gene FAT1 has a mutation status of S2682Ter, The gene AGXT2 has a mutation status of E175K, The gene ARSB has a mutation status of R489K, The gene PCDHGA6 has a mutation status of D411Y, The gene PCDHGA10 has a mutation status of E148K, The gene PCDHGA12 has a mutation status of R282Q, The gene NQO2 has a mutation status of R50G, The gene FAM8A1 has a mutation status of E253Q, The gene BAG6 has a mutation status of M509I, The gene HLA-DQB1 has a mutation status of P84E, The gene PHF1 has a mutation status of D274N, The gene IRAK1BP1 has a mutation status of E147Q, The gene PREP has a mutation status of Q388R, The gene HIVEP2 has a mutation status of L2305F, The gene FNDC1 has a mutation status of P1258S, The gene CDK13 has a mutation status of E1019Ter, The gene TRIP6 has a mutation status of F363L, The gene MYL10 has a mutation status of D226V, The gene LRWD1 has a mutation status of E340A, The gene SRPK2 has a mutation status of D65A, The gene CUL1 has a mutation status of S114T, The gene NOS3 has a mutation status of S114F, The gene GPAT4 has a mutation status of A34V, The gene MAFA has a mutation status of G328R, The gene RUSC2 has a mutation status of L231R, The gene ZBTB5 has a mutation status of D82N, The gene ERCC6L2 has a mutation status of P100A, The gene NR5A1 has a mutation status of E7K, The gene MVB12B has a mutation status of V53I, The gene PRDM12 has a mutation status of K319R, The gene CACNA1B has a mutation status of R1062Q, The gene MT-ND1 has a mutation status of A147T, The gene MT-CO3 has a mutation status of A200T, The gene PNPLA4 has a mutation status of E72Q, The gene DCAF8L2 has a mutation status of N310S, The gene FAM47C has a mutation status of A132V, The gene KDM6A has a mutation status of E947Ter, The gene PHKA1 has a mutation status of G1001W, The gene XPNPEP2 has a mutation status of G453R, The gene HCFC1 has a mutation status of A1353S, The gene MEGF6 has a mutation status of Q117E, The gene PLOD1 has a mutation status of G156D, The gene SPEN has a mutation status of E1965del, The gene ZMYM4 has a mutation status of N788KfsTer40, The gene P3H1 has a mutation status of L258RfsTer5, The gene B4GALT2 has a mutation status of F212V, The gene TTC22 has a mutation status of D362E, The gene KANK4 has a mutation status of E262Ter, The gene LRRIQ3 has a mutation status of M588I, The gene CCN1 has a mutation status of G184E, The gene CLCA4 has a mutation status of H100Y, The gene STRIP1 has a mutation status of P21Q, The gene CD101 has a mutation status of R376K, The gene RPRD2 has a mutation status of S545N, The gene FLG has a mutation status of H2618N, The gene UBAP2L has a mutation status of S673Ter, The gene ASH1L has a mutation status of R1852L, The gene ETV3L has a mutation status of E319D, The gene CD244 has a mutation status of T193I, The gene HMCN1 has a mutation status of E5601K, The gene PROX1 has a mutation status of P728L, The gene DNAH14 has a mutation status of K3288N, The gene OBSCN has a mutation status of A2212L, The gene RYR2 has a mutation status of R2401H, The gene WDR64 has a mutation status of S731N, The gene CUBN has a mutation status of H2366N, The gene NEBL has a mutation status of S898A, The gene ENKUR has a mutation status of N77S, The gene GAD2 has a mutation status of A406V, The gene SVIL has a mutation status of R1766S, The gene UNC5B has a mutation status of L909R, The gene SEC31B has a mutation status of W149L, The gene STK32C has a mutation status of S457Y, The gene STK32C has a mutation status of P455T, The gene CFAP46 has a mutation status of E1950D, The gene TUBGCP2 has a mutation status of G348SfsTer56, The gene HRAS has a mutation status of G12V, The gene PIDD1 has a mutation status of A308S, The gene MUC5AC has a mutation status of A5353K, The gene MUC5B has a mutation status of T301I, The gene MUC5B has a mutation status of E1350K, The gene OR52D1 has a mutation status of L225H, The gene HARBI1 has a mutation status of Y15H, The gene OR5D13 has a mutation status of Q198H, The gene OR5D18 has a mutation status of A275V, The gene C2CD3 has a mutation status of R2252K, The gene ALG8 has a mutation status of Y514C, The gene DLG2 has a mutation status of I197V, The gene ATM has a mutation status of K2440R, The gene SORL1 has a mutation status of E746Ter, The gene ADAMTS8 has a mutation status of T223A, The gene CACNA2D4 has a mutation status of V298L, The gene PRMT8 has a mutation status of Q35P, The gene FGF6 has a mutation status of D50E, The gene ALG10B has a mutation status of D218N, The gene LRRK2 has a mutation status of T2158I, The gene MUC19 has a mutation status of Y4423S, The gene MUC19 has a mutation status of N6618_I6619delinsSV, The gene FAM186B has a mutation status of F616C, The gene OR2AP1 has a mutation status of S36I, The gene HSD17B6 has a mutation status of Y181Ter, The gene WIF1 has a mutation status of A149E, The gene LRRC10 has a mutation status of L103F, The gene MYRFL has a mutation status of P659Q, The gene E2F7 has a mutation status of Q138H, The gene FGD6 has a mutation status of S782C, The gene SLC5A8 has a mutation status of G421D, The gene ATXN2 has a mutation status of E246K, The gene KSR2 has a mutation status of S731I, The gene KDM2B has a mutation status of T267S, The gene ADGRD1 has a mutation status of C574F, The gene CRYL1 has a mutation status of T240I, The gene MTUS2 has a mutation status of G215A, The gene SLAIN1 has a mutation status of G168A, The gene AKAP6 has a mutation status of E670Ter, The gene PCNX1 has a mutation status of W2286EfsTer37, The gene MKRN3 has a mutation status of E9D, The gene APBA2 has a mutation status of A397V, The gene ATP8B4 has a mutation status of S259G, The gene GNB5 has a mutation status of I349F, The gene UNC13C has a mutation status of Q1582H, The gene EDC3 has a mutation status of G208E, The gene AP3B2 has a mutation status of A953S, The gene ANPEP has a mutation status of S613R, The gene PKD1 has a mutation status of R2213Q, The gene SEZ6L2 has a mutation status of H659N, The gene HEATR3 has a mutation status of A436V, The gene CDYL2 has a mutation status of V135L, The gene CLUH has a mutation status of I1250M, The gene SPNS3 has a mutation status of A276S, The gene ALOX15 has a mutation status of T537S, The gene POLR2A has a mutation status of E1152Q, The gene POLR2A has a mutation status of E1188Q, The gene POLR2A has a mutation status of D1223N, The gene TP53 has a mutation status of Y126Ter, The gene TRAPPC1 has a mutation status of L37V, The gene NTN1 has a mutation status of S67C, The gene MYH3 has a mutation status of E1788K, The gene EPOP has a mutation status of E2Ter, The gene FBXO47 has a mutation status of L224F, The gene MED1 has a mutation status of A96T, The gene C17orf113 has a mutation status of R301L, The gene C17orf113 has a mutation status of G169C, The gene TTLL6 has a mutation status of K728Ter, The gene DHX40 has a mutation status of P87S, The gene POLG2 has a mutation status of H313N, The gene AXIN2 has a mutation status of R675VfsTer14, The gene ABCA10 has a mutation status of W270C, The gene PIEZO2 has a mutation status of S2690Ter, The gene ASXL3 has a mutation status of Q1897K, The gene EPG5 has a mutation status of L361GfsTer12, The gene CCDC68 has a mutation status of E80Q, The gene ONECUT2 has a mutation status of G45S, The gene CDH19 has a mutation status of K630N, The gene MEX3D has a mutation status of A82V, The gene COL5A3 has a mutation status of V1162I, The gene STX10 has a mutation status of D196V, The gene ADGRL1 has a mutation status of A6RfsTer37, The gene PKN1 has a mutation status of P337T, The gene WIZ has a mutation status of H88Y, The gene ZNF729 has a mutation status of C908S, The gene CD22 has a mutation status of P429L, The gene FFAR2 has a mutation status of N293S, The gene HAUS5 has a mutation status of A627S, The gene RASGRP4 has a mutation status of S194F, The gene ZC3H4 has a mutation status of P990S, The gene GRIN2D has a mutation status of A1092T, The gene RASIP1 has a mutation status of A951G, The gene IZUMO2 has a mutation status of M178I, The gene ZNF845 has a mutation status of E884D, The gene AURKC has a mutation status of R165K, The gene PXDN has a mutation status of D1432H, The gene KIDINS220 has a mutation status of S1462L, The gene SMC6 has a mutation status of L216I, The gene GDF7 has a mutation status of C414Ter, The gene APOB has a mutation status of D2277E, The gene CAD has a mutation status of V1357F, The gene FOSL2 has a mutation status of G205AfsTer53, The gene TET3 has a mutation status of R160T, The gene LIPT1 has a mutation status of H239N, The gene FHL2 has a mutation status of R242W, The gene SLC35F5 has a mutation status of I272V, The gene R3HDM1 has a mutation status of F1094I, The gene GALNT5 has a mutation status of E564G, The gene UBR3 has a mutation status of S325Y, The gene FSIP2 has a mutation status of S3169P, The gene SATB2 has a mutation status of S299Y, The gene STRADB has a mutation status of Y245C, The gene TMEM237 has a mutation status of R192H, The gene IGFBP5 has a mutation status of S145F, The gene ZNF142 has a mutation status of E416K, The gene MTERF4 has a mutation status of Q75PfsTer3, The gene ZNF337 has a mutation status of Q619E, The gene TPX2 has a mutation status of S121C, The gene EFCAB8 has a mutation status of H313Y, The gene BPIFA1 has a mutation status of G86D, The gene MMP24 has a mutation status of A68E, The gene PCIF1 has a mutation status of A552G, The gene CDH22 has a mutation status of G712A, The gene TCFL5 has a mutation status of R186H, The gene DIDO1 has a mutation status of E140Q, The gene NCAM2 has a mutation status of K806N, The gene ADAMTS5 has a mutation status of G171E, The gene MCM3AP has a mutation status of C1561R, The gene C21orf58 has a mutation status of A222P, The gene IGLV3-32 has a mutation status of D70H, The gene MTMR3 has a mutation status of H991Y, The gene SFI1 has a mutation status of Y152Ter, The gene SLC5A4 has a mutation status of D585Y, The gene EP300 has a mutation status of C1201Y, The gene ZBED4 has a mutation status of K292Q, The gene TMEM40 has a mutation status of K49E, The gene RFTN1 has a mutation status of Q537L, The gene CCR1 has a mutation status of L331H, The gene TCTA has a mutation status of H101D, The gene CRYBG3 has a mutation status of E2763Ter, The gene EFCC1 has a mutation status of V281M, The gene AMOTL2 has a mutation status of R547Ter, The gene XRN1 has a mutation status of P1646S, The gene SLITRK3 has a mutation status of T567N, The gene LPP has a mutation status of C476Ter, The gene ATP13A5 has a mutation status of Q1212E, The gene MUC4 has a mutation status of A2782_H2797del, The gene MUC4 has a mutation status of L1410H, The gene LDB2 has a mutation status of G333N, The gene SLC9B2 has a mutation status of S298F, The gene TBCK has a mutation status of S277Ter, The gene RNF150 has a mutation status of P329L, The gene OTUD4 has a mutation status of S1072EfsTer10, The gene OTUD4 has a mutation status of E1071SfsTer53, The gene FHDC1 has a mutation status of A680S, The gene CEP44 has a mutation status of M213I, The gene ADAM29 has a mutation status of H333D, The gene FAT1 has a mutation status of S2682Ter, The gene TRIO has a mutation status of D1310N, The gene AGXT2 has a mutation status of E175K, The gene UGT3A2 has a mutation status of L158I, The gene NIPBL has a mutation status of R808Ter, The gene NIPBL has a mutation status of E844Q, The gene NIPBL has a mutation status of A1308P, The gene NIM1K has a mutation status of V139L, The gene AP3B1 has a mutation status of K923NfsTer4, The gene ARSB has a mutation status of R489K, The gene PCDHGA6 has a mutation status of D411Y, The gene PCDHGA10 has a mutation status of E148K, The gene PCDHGA12 has a mutation status of R282Q, The gene ARHGEF37 has a mutation status of L183M, The gene SLIT3 has a mutation status of T209I, The gene NQO2 has a mutation status of R50G, The gene FAM8A1 has a mutation status of E253Q, The gene MUC21 has a mutation status of T323V, The gene BAG6 has a mutation status of M509I, The gene HLA-DRB1 has a mutation status of S66N, The gene HLA-DRB1 has a mutation status of W38E, The gene PHF1 has a mutation status of D274N, The gene RAB44 has a mutation status of R995G, The gene DEFB112 has a mutation status of P18T, The gene BMP5 has a mutation status of K72I, The gene ADGRB3 has a mutation status of S923Ter, The gene IRAK1BP1 has a mutation status of E147Q, The gene HACE1 has a mutation status of S709Y, The gene REV3L has a mutation status of I1994L, The gene HIVEP2 has a mutation status of L2305F, The gene SCAF8 has a mutation status of I1027N, The gene CYTH3 has a mutation status of K82E, The gene ZNF316 has a mutation status of R702H, The gene CDK13 has a mutation status of E1019Ter, The gene CCM2 has a mutation status of G377S, The gene ADCY1 has a mutation status of A59E, The gene ZNF727 has a mutation status of M33I, The gene MLXIPL has a mutation status of P491L, The gene PCLO has a mutation status of Q462H, The gene TRIP6 has a mutation status of F363L, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S537P, The gene MYL10 has a mutation status of D226V, The gene SRPK2 has a mutation status of D65A, The gene RNF148 has a mutation status of N33S, The gene TBXAS1 has a mutation status of H165N, The gene MGAM2 has a mutation status of R1566I, The gene NOBOX has a mutation status of H479Y, The gene CUL1 has a mutation status of S114T, The gene NOS3 has a mutation status of S114F, The gene MNX1 has a mutation status of A124T, The gene MNX1 has a mutation status of G108R, The gene RP1L1 has a mutation status of D2375E, The gene GPAT4 has a mutation status of A34V, The gene PI15 has a mutation status of C245Y, The gene LY6K has a mutation status of F75Y, The gene MAFA has a mutation status of G328R, The gene DOCK8 has a mutation status of E1498D, The gene DOCK8 has a mutation status of D1564E, The gene TAF1L has a mutation status of G979VfsTer7, The gene RUSC2 has a mutation status of L231R, The gene ZBTB5 has a mutation status of D82N, The gene PRUNE2 has a mutation status of D514E, The gene FOXB2 has a mutation status of P188L, The gene ERCC6L2 has a mutation status of P100A, The gene PLPPR1 has a mutation status of E89D, The gene CNTRL has a mutation status of V656F, The gene COQ4 has a mutation status of L112V, The gene CERCAM has a mutation status of Q162K, The gene CACNA1B has a mutation status of R1062Q, The gene MT-ND1 has a mutation status of A147T, The gene MT-CO3 has a mutation status of A200T, The gene PNPLA4 has a mutation status of E72Q, The gene KDM6A has a mutation status of E947Ter, The gene AKAP4 has a mutation status of N641K, The gene PHKA1 has a mutation status of G1001W, The gene AMOT has a mutation status of S215I, The gene TENM1 has a mutation status of L1600I, The gene XPNPEP2 has a mutation status of G453R, The gene HCFC1 has a mutation status of A1353S, The gene EMD has a mutation status of G218R, The gene PADI2 has a mutation status of P655T, The gene ARHGEF10L has a mutation status of G594E, The gene ARID1A has a mutation status of L184AfsTer215, The gene ZC3H12A has a mutation status of E84D, The gene POU3F1 has a mutation status of A114V, The gene ERMAP has a mutation status of P450L, The gene BSND has a mutation status of I12N, The gene HOOK1 has a mutation status of F657L, The gene WLS has a mutation status of R220W, The gene GBP3 has a mutation status of D190Y, The gene RSBN1 has a mutation status of V85L, The gene LCE1F has a mutation status of K19R, The gene BCAN has a mutation status of C650S, The gene INSRR has a mutation status of G674S, The gene BTG2 has a mutation status of Q140E, The gene USH2A has a mutation status of V2562D, The gene ITPKB has a mutation status of S86N, The gene ITPKB has a mutation status of C5Ter, The gene PSEN2 has a mutation status of P321L, The gene IRF2BP2 has a mutation status of H315D, The gene TRIM58 has a mutation status of P5L, The gene SVIL has a mutation status of R1870W, The gene ARID5B has a mutation status of L57F, The gene TET1 has a mutation status of S911_D916delinsY, The gene DDIT4 has a mutation status of S48R, The gene WAPL has a mutation status of I404RfsTer6, The gene LDB3 has a mutation status of R178W, The gene IDE has a mutation status of D895N, The gene MUC5B has a mutation status of R5517C, The gene KRTAP5-5 has a mutation status of C160G, The gene WEE1 has a mutation status of G135S, The gene WEE1 has a mutation status of G153R, The gene WEE1 has a mutation status of H176Y, The gene WEE1 has a mutation status of E301D, The gene ADM has a mutation status of I90M, The gene RRAS2 has a mutation status of G24_G26du, The gene OR4C45 has a mutation status of A73D, The gene TNKS1BP1 has a mutation status of V1367G, The gene PYGM has a mutation status of K575T, The gene LTBP3 has a mutation status of T283S, The gene CD248 has a mutation status of P127L, The gene B4GAT1 has a mutation status of Q344Ter, The gene RSF1 has a mutation status of R849W, The gene PCF11 has a mutation status of S33N, The gene KDM4F has a mutation status of T612S, The gene CNTN5 has a mutation status of P429TfsTer7, The gene VWA5A has a mutation status of V114M, The gene SCNN1A has a mutation status of R181W, The gene CLEC4C has a mutation status of H197N, The gene IRAG2 has a mutation status of T330R, The gene RESF1 has a mutation status of S1562N, The gene KMT2D has a mutation status of Q3991Ter, The gene BCDIN3D has a mutation status of V23I, The gene HSD17B6 has a mutation status of G10S, The gene SRGAP1 has a mutation status of K315T, The gene DTX1 has a mutation status of A246V, The gene SKA3 has a mutation status of E234K, The gene FOXO1 has a mutation status of S33C, The gene TBC1D4 has a mutation status of A140P, The gene SLC39A2 has a mutation status of V215A, The gene ZFHX2 has a mutation status of T2563S, The gene NFKBIA has a mutation status of Q255Ter, The gene NID2 has a mutation status of H511Y, The gene SLC35F4 has a mutation status of S320R, The gene KCNH5 has a mutation status of H570Y, The gene ZFP36L1 has a mutation status of L144F, The gene ZFP36L1 has a mutation status of C129Y, The gene FLRT2 has a mutation status of C49S, The gene IGHA2 has a mutation status of T348A, The gene IGHE has a mutation status of S413R, The gene IGHE has a mutation status of E410D, The gene IGHE has a mutation status of S382C, The gene IGHE has a mutation status of G381D, The gene IGHE has a mutation status of V357L, The gene IGHE has a mutation status of K340R, The gene IGHE has a mutation status of C299F, The gene IGHE has a mutation status of A245T, The gene IGHE has a mutation status of T192I, The gene IGHE has a mutation status of L72PfsTer15, The gene IGHG1 has a mutation status of Q302Ter, The gene IGHG1 has a mutation status of Q178HfsTer59, The gene IGHG1 has a mutation status of V56YfsTer13, The gene IGHG1 has a mutation status of G20W, The gene IGHG3 has a mutation status of P132T, The gene IGHG3 has a mutation status of V39M, The gene IGHG3 has a mutation status of V8F, The gene RTF1 has a mutation status of E26WfsTer44, The gene STARD9 has a mutation status of T3046P, The gene DIS3L has a mutation status of S53R, The gene SMAD6 has a mutation status of A449T, The gene SCAMP2 has a mutation status of N329T, The gene MAN2C1 has a mutation status of S706C, The gene SIN3A has a mutation status of E613K, The gene MCTP2 has a mutation status of I767M, The gene CREBBP has a mutation status of Q676Ter, The gene SOCS1 has a mutation status of Q175E, The gene SOCS1 has a mutation status of H129N, The gene GSPT1 has a mutation status of N106K, The gene ZP2 has a mutation status of N621T, The gene RBBP6 has a mutation status of L114F, The gene PHKB has a mutation status of N864I, The gene PLCG2 has a mutation status of P442L, The gene ZFPM1 has a mutation status of F525V, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene ANKFY1 has a mutation status of I884T, The gene SLC52A1 has a mutation status of V369G, The gene NLGN2 has a mutation status of H807P, The gene MYO15A has a mutation status of I2576M, The gene EVPLL has a mutation status of Q234H, The gene EPN2 has a mutation status of Q245H, The gene FLOT2 has a mutation status of L47V, The gene DHRS13 has a mutation status of A123V, The gene PIGW has a mutation status of A379G, The gene ACACA has a mutation status of L586F, The gene MEIOC has a mutation status of N524I, The gene ITGA3 has a mutation status of V373GfsTer5, The gene TEX14 has a mutation status of Y912C, The gene GNA13 has a mutation status of I88del, The gene GNA13 has a mutation status of Q27H, The gene HELZ has a mutation status of G359V, The gene ABCA6 has a mutation status of D959N, The gene MYO15B has a mutation status of R341S, The gene ESCO1 has a mutation status of L496W, The gene KLHL14 has a mutation status of M261I, The gene KLHL14 has a mutation status of Q188E, The gene KLHL14 has a mutation status of V147L, The gene KLHL14 has a mutation status of L139I, The gene LMAN1 has a mutation status of T413I, The gene BCL2 has a mutation status of A45T, The gene BCL2 has a mutation status of P44R, The gene HCN2 has a mutation status of D2A, The gene POLRMT has a mutation status of P741L, The gene ARHGEF18 has a mutation status of S948N, The gene ICAM1 has a mutation status of L118V, The gene DOCK6 has a mutation status of L1405V, The gene ZNF878 has a mutation status of E162G, The gene JUND has a mutation status of L197V, The gene NCAN has a mutation status of S135F, The gene ZNF506 has a mutation status of P74L, The gene ANKRD27 has a mutation status of A945P, The gene PSG3 has a mutation status of P3T, The gene SLC8A2 has a mutation status of I337M, The gene RASIP1 has a mutation status of P859H, The gene TULP2 has a mutation status of F318V, The gene PPFIA3 has a mutation status of N919K, The gene PRR12 has a mutation status of N1373Y, The gene SIGLEC7 has a mutation status of E251D, The gene ZNF175 has a mutation status of M56I, The gene LILRB4 has a mutation status of K362P, The gene PTPRH has a mutation status of A1084S, The gene KCNK12 has a mutation status of R71H, The gene KCNK12 has a mutation status of E34DfsTer87, The gene SPTBN1 has a mutation status of H1808Y, The gene USP34 has a mutation status of E2202V, The gene SFXN5 has a mutation status of P159S, The gene SLC4A5 has a mutation status of L259V, The gene DUSP2 has a mutation status of G130R, The gene CNNM4 has a mutation status of I265L, The gene INPP4A has a mutation status of E912K, The gene IL1RL2 has a mutation status of W513Ter, The gene BCL2L11 has a mutation status of E39SfsTer45, The gene IMP4 has a mutation status of Y12N, The gene GPR148 has a mutation status of T262S, The gene TBR1 has a mutation status of Y581S, The gene TTN has a mutation status of L19615M, The gene ZNF804A has a mutation status of E896D, The gene FSIP2 has a mutation status of S1995Y, The gene ZDBF2 has a mutation status of I1570V, The gene LANCL1 has a mutation status of R41L, The gene CPS1 has a mutation status of K841R, The gene FEV has a mutation status of Y212D, The gene CUL3 has a mutation status of G7V, The gene UGT1A4 has a mutation status of S21VfsTer45, The gene ERFE has a mutation status of L188R, The gene SNX5 has a mutation status of Q11Ter, The gene SALL4 has a mutation status of G747S, The gene BMP7 has a mutation status of A8T, The gene ZNF831 has a mutation status of E160D, The gene DIDO1 has a mutation status of S2007L, The gene DONSON has a mutation status of N510T, The gene TSPEAR has a mutation status of E257Ter, The gene IGLV6-57 has a mutation status of S88N, The gene IGLL5 has a mutation status of G19S, The gene IGLC2 has a mutation status of R83S, The gene BCR has a mutation status of P20S, The gene BCR has a mutation status of I31WfsTer15, The gene BCR has a mutation status of P99S, The gene BCR has a mutation status of A137D, The gene BCR has a mutation status of S281N, The gene SMARCB1 has a mutation status of M217L, The gene SPECC1L has a mutation status of S48A, The gene KIAA1671 has a mutation status of A1203S, The gene EDEM1 has a mutation status of R36H, The gene EDEM1 has a mutation status of L126V, The gene NUP210 has a mutation status of F1044V, The gene ZNF502 has a mutation status of L506F, The gene ADAMTS9 has a mutation status of F657L, The gene PDZRN3 has a mutation status of A39D, The gene IMPG2 has a mutation status of H675N, The gene LSAMP has a mutation status of V211I, The gene FSTL1 has a mutation status of E188D, The gene ZXDC has a mutation status of L42V, The gene MED12L has a mutation status of P1937S, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene DLG1 has a mutation status of D677N, The gene HGFAC has a mutation status of P181L, The gene BLOC1S4 has a mutation status of S6Ter, The gene LDB2 has a mutation status of K282N, The gene NWD2 has a mutation status of L1197I, The gene UTP3 has a mutation status of Q68Ter, The gene SHROOM3 has a mutation status of P979L, The gene UNC5C has a mutation status of L856Q, The gene TERT has a mutation status of W478Ter, The gene RAB3C has a mutation status of T94N, The gene IPO11 has a mutation status of P285R, The gene LMNB1 has a mutation status of L75F, The gene CDC25C has a mutation status of S146G, The gene PCDHB3 has a mutation status of L303Q, The gene PCDHGB1 has a mutation status of T105M, The gene RNF44 has a mutation status of Q193PfsTer145, The gene FOXC1 has a mutation status of C395SfsTer130, The gene GMPR has a mutation status of S246P, The gene H1-2 has a mutation status of S104C, The gene H1-2 has a mutation status of T92S, The gene H1-4 has a mutation status of A123S, The gene H4C4 has a mutation status of G14S, The gene H2BC8 has a mutation status of G76D, The gene H2BC12 has a mutation status of Q48Ter, The gene OR2H1 has a mutation status of D63N, The gene TRIM10 has a mutation status of D113E, The gene NFKBIL1 has a mutation status of F297V, The gene VARS1 has a mutation status of E1234Ter, The gene EHMT2 has a mutation status of N403T, The gene HLA-DRB5 has a mutation status of A133L, The gene HLA-DQB1 has a mutation status of Y69I, The gene HLA-DQB1 has a mutation status of Y62S, The gene RPL10A has a mutation status of R48G, The gene PIM1 has a mutation status of M1?, The gene PIM1 has a mutation status of A22G, The gene PIM1 has a mutation status of P81S, The gene TFAP2B has a mutation status of S266C, The gene ASCC3 has a mutation status of R1108K, The gene KIAA0408 has a mutation status of N511T, The gene ARID1B has a mutation status of A93V, The gene ARID1B has a mutation status of A173G, The gene ARID1B has a mutation status of S222T, The gene IGF2R has a mutation status of I2193V, The gene CARD11 has a mutation status of S690N, The gene TNRC18 has a mutation status of Q1353H, The gene INTS15 has a mutation status of D154E, The gene ZNRF2 has a mutation status of P24L, The gene BBS9 has a mutation status of Y623Ter, The gene PCLO has a mutation status of L3223V, The gene PPP1R9A has a mutation status of S460C, The gene MUC17 has a mutation status of S3249P, The gene KMT2E has a mutation status of S861N, The gene KCP has a mutation status of S516C, The gene AKR1B10 has a mutation status of H164Y, The gene AKR1D1 has a mutation status of H62N, The gene EZH2 has a mutation status of Y646F, The gene SMARCD3 has a mutation status of P170T, The gene CSMD1 has a mutation status of A3212D, The gene MFHAS1 has a mutation status of A394T, The gene MFHAS1 has a mutation status of L56I, The gene MFHAS1 has a mutation status of N28T, The gene POLR3D has a mutation status of G4I, The gene COL14A1 has a mutation status of V40L, The gene MYC has a mutation status of P72T, The gene MYC has a mutation status of S79N, The gene MYC has a mutation status of V279L, The gene OC90 has a mutation status of H349Q, The gene PLEC has a mutation status of D3868A, The gene PLEC has a mutation status of L1238R, The gene GRIN3A has a mutation status of R981T, The gene ALAD has a mutation status of A211T, The gene HMCN2 has a mutation status of A4166G, The gene FUBP3 has a mutation status of V410I, The gene TUBB4B has a mutation status of A231S, The gene MT-ND4 has a mutation status of A318T, The gene MT-ND6 has a mutation status of T156I, The gene MT-CYB has a mutation status of T194A, The gene MAP3K15 has a mutation status of P831S, The gene DDX3X has a mutation status of Y291C, The gene GATA1 has a mutation status of Q17K, The gene GPKOW has a mutation status of P200R, The gene SHROOM4 has a mutation status of Q812R, The gene SHROOM4 has a mutation status of K805R, The gene ATRX has a mutation status of K1001E, The gene THOC2 has a mutation status of M746T, The gene TREX2 has a mutation status of L114F	BLCA
The gene ESPN has a mutation status of P452T, The gene PEX14 has a mutation status of S265L, The gene EYA3 has a mutation status of V366L, The gene ZMYM6 has a mutation status of D664G, The gene NT5C1A has a mutation status of A352V, The gene SZT2 has a mutation status of A317G, The gene ADGRL2 has a mutation status of W163Ter, The gene FMO5 has a mutation status of I530T, The gene S100A10 has a mutation status of A77V, The gene SMCP has a mutation status of C65Ter, The gene PRRC2C has a mutation status of K535R, The gene ASPM has a mutation status of R3392K, The gene PGBD5 has a mutation status of H465Y, The gene LYST has a mutation status of L2438Q, The gene WDR64 has a mutation status of H375Y, The gene GATA3 has a mutation status of D336GfsTer17, The gene SLC39A12 has a mutation status of W446Ter, The gene ZNF22 has a mutation status of G27V, The gene WDFY4 has a mutation status of V2122L, The gene ERCC6 has a mutation status of S1099R, The gene ERCC6 has a mutation status of V83I, The gene CSTF2T has a mutation status of Q167Ter, The gene SLC25A16 has a mutation status of G299A, The gene EIF4EBP2 has a mutation status of S14R, The gene MRPS16 has a mutation status of N69K, The gene NDST2 has a mutation status of R502G, The gene LIPF has a mutation status of S134A, The gene PIK3AP1 has a mutation status of E50K, The gene MUC6 has a mutation status of P1487L, The gene OR52P1 has a mutation status of G74S, The gene DNHD1 has a mutation status of E4427K, The gene HTATIP2 has a mutation status of L170V, The gene NELL1 has a mutation status of E417V, The gene PRG3 has a mutation status of C107Ter, The gene DAGLA has a mutation status of H471Y, The gene NRXN2 has a mutation status of Q1173K, The gene RBM14 has a mutation status of T454S, The gene CLPB has a mutation status of K10delinsNL, The gene C2CD3 has a mutation status of H2035L, The gene POLD3 has a mutation status of E137K, The gene TPBGL has a mutation status of A247V, The gene FAM181B has a mutation status of G306S, The gene CEP126 has a mutation status of H1081Y, The gene DDX10 has a mutation status of H27R, The gene NCAPD3 has a mutation status of A688D, The gene C12orf4 has a mutation status of R335Q, The gene TAS2R30 has a mutation status of I33T, The gene IRAG2 has a mutation status of A714S, The gene FAM186B has a mutation status of W566C, The gene KRT2 has a mutation status of Q161H, The gene IKZF4 has a mutation status of T19N, The gene BAZ2A has a mutation status of E621Ter, The gene BBS10 has a mutation status of G401E, The gene HVCN1 has a mutation status of A16G, The gene ATP6V0A2 has a mutation status of S659C, The gene ADGRD1 has a mutation status of Q37H, The gene SMAD9 has a mutation status of V42L, The gene NUDT15 has a mutation status of E151K, The gene DLEU7 has a mutation status of S129L, The gene JPH4 has a mutation status of R233C, The gene KIAA0586 has a mutation status of L1422I, The gene GPR68 has a mutation status of Q95H, The gene COX8C has a mutation status of P38S, The gene PPP4R4 has a mutation status of D283Y, The gene SLC25A29 has a mutation status of P37L, The gene IGHA2 has a mutation status of T348S, The gene IGHM has a mutation status of E418Q, The gene IGHV4-59 has a mutation status of E35Q, The gene VPS18 has a mutation status of L869F, The gene ONECUT1 has a mutation status of C321Y, The gene UBAP1L has a mutation status of A124V, The gene SMAD3 has a mutation status of V134F, The gene ADPGK has a mutation status of E216K, The gene ULK3 has a mutation status of R422_R423del, The gene AGBL1 has a mutation status of E167D, The gene CACNA1H has a mutation status of M611I, The gene PPL has a mutation status of E1254K, The gene ZNF778 has a mutation status of T444GfsTer8, The gene NLRP1 has a mutation status of P242Q, The gene KRT32 has a mutation status of P427I, The gene HOXB7 has a mutation status of E216Ter, The gene KIF2B has a mutation status of D546N, The gene ACE has a mutation status of S233F, The gene UNK has a mutation status of S517C, The gene QRICH2 has a mutation status of D262E, The gene CYTH1 has a mutation status of E40K, The gene CBX8 has a mutation status of S316Y, The gene PTPRM has a mutation status of D1076H, The gene SERPINB2 has a mutation status of E160Ter, The gene PCSK4 has a mutation status of G302S, The gene MUC16 has a mutation status of D13719Y, The gene MUC16 has a mutation status of P13632LfsTer60, The gene CPAMD8 has a mutation status of D684N, The gene ZNF254 has a mutation status of H620N, The gene ZNF610 has a mutation status of G210C, The gene LAIR1 has a mutation status of A266VfsTer57, The gene RAD51AP2 has a mutation status of D698E, The gene TDRD15 has a mutation status of G1405R, The gene PPM1G has a mutation status of E451K, The gene ETAA1 has a mutation status of S833FfsTer8, The gene EXOC6B has a mutation status of G4A, The gene ACTG2 has a mutation status of E242K, The gene KDM3A has a mutation status of A765V, The gene CKAP2L has a mutation status of L599FfsTer14, The gene CKAP2L has a mutation status of P91Q, The gene XIRP2 has a mutation status of I3408T, The gene TTN has a mutation status of C31877S, The gene TTN has a mutation status of A26363D, The gene KANSL1L has a mutation status of N615S, The gene ERBB4 has a mutation status of Y1242C, The gene IRS1 has a mutation status of R327C, The gene SCYGR2 has a mutation status of H97S, The gene MKKS has a mutation status of N366Y, The gene SYCP2 has a mutation status of M477L, The gene BRWD1 has a mutation status of P621S, The gene BCL2L13 has a mutation status of S5LfsTer40, The gene PI4KA has a mutation status of D584E, The gene SUSD2 has a mutation status of D77Y, The gene GGT5 has a mutation status of F302L, The gene KIAA1671 has a mutation status of Q1220Ter, The gene SLC5A1 has a mutation status of I397T, The gene MYH9 has a mutation status of K682_L687del, The gene CSDC2 has a mutation status of D111N, The gene UBA3 has a mutation status of A380G, The gene NECTIN3 has a mutation status of P45DfsTer13, The gene NECTIN3 has a mutation status of P45T, The gene CD200 has a mutation status of Q102K, The gene HLTF has a mutation status of V287F, The gene KCNAB1 has a mutation status of G159D, The gene TNIK has a mutation status of G884V, The gene PIK3CA has a mutation status of E545K, The gene MAP3K13 has a mutation status of D380N, The gene CLDN1 has a mutation status of Q163L, The gene MUC4 has a mutation status of A4086T, The gene MUC4 has a mutation status of S1669D, The gene HMX1 has a mutation status of P291T, The gene LIAS has a mutation status of M310T, The gene ATP10D has a mutation status of Y81S, The gene EPHA5 has a mutation status of L987P, The gene TMPRSS11B has a mutation status of V56G, The gene PRKG2 has a mutation status of R259Ter, The gene FAM13A has a mutation status of N217K, The gene DCHS2 has a mutation status of E1201A, The gene CLCN3 has a mutation status of W555Ter, The gene TENM3 has a mutation status of P1998H, The gene ZFP42 has a mutation status of G65E, The gene ADAMTS16 has a mutation status of R1158Q, The gene SEMA5A has a mutation status of P45H, The gene ISL1 has a mutation status of R130P, The gene MAST4 has a mutation status of K2433Q, The gene PDE8B has a mutation status of R426Q, The gene ACOT12 has a mutation status of A403N, The gene XRCC4 has a mutation status of K197R, The gene RGMB has a mutation status of G286S, The gene JAKMIP2 has a mutation status of I265V, The gene SQSTM1 has a mutation status of E101D, The gene HLA-DQB1 has a mutation status of P84E, The gene HLA-DQB1 has a mutation status of Y62S, The gene HLA-DQB2 has a mutation status of V37Y, The gene CLPSL1 has a mutation status of C57W, The gene SLC26A8 has a mutation status of G964C, The gene KIF6 has a mutation status of R600del, The gene EYS has a mutation status of K1077N, The gene COL9A1 has a mutation status of G364C, The gene SNAP91 has a mutation status of A366S, The gene EPHA7 has a mutation status of V418L, The gene TRDN has a mutation status of E519K, The gene TAAR6 has a mutation status of Y311H, The gene ALDH8A1 has a mutation status of P319S, The gene RMND1 has a mutation status of F369L, The gene PDK4 has a mutation status of A144T, The gene RELN has a mutation status of E2374K, The gene PLXNA4 has a mutation status of W8C, The gene ZNF467 has a mutation status of V508M, The gene GIMAP7 has a mutation status of S73R, The gene ASB10 has a mutation status of G248V, The gene SH2D4A has a mutation status of P161T, The gene RP1 has a mutation status of G1355R, The gene NBN has a mutation status of R43Ter, The gene ZFPM2 has a mutation status of E800Q, The gene HHLA1 has a mutation status of N85S, The gene JRK has a mutation status of K115R, The gene CYP11B2 has a mutation status of A414P, The gene CPSF1 has a mutation status of R63W, The gene GPT has a mutation status of P472S, The gene KCNV2 has a mutation status of H26Q, The gene PTPRD has a mutation status of Q1597Ter, The gene CCDC171 has a mutation status of E551V, The gene PRSS3 has a mutation status of G208R, The gene SHC3 has a mutation status of M1?, The gene WNK2 has a mutation status of L312Q, The gene TRMO has a mutation status of S191Y, The gene NIPSNAP3B has a mutation status of N82K, The gene PTPN3 has a mutation status of M403I, The gene SVEP1 has a mutation status of A1142S, The gene TTC16 has a mutation status of D373N, The gene LRRC8A has a mutation status of T170M, The gene PPP1R26 has a mutation status of A1185S, The gene MT-CO3 has a mutation status of V254I, The gene MT-ND6 has a mutation status of N119D, The gene MT-CYB has a mutation status of T212A, The gene FAM47A has a mutation status of W705Ter, The gene HUWE1 has a mutation status of L3620F, The gene PHF8 has a mutation status of H31P, The gene KIF4A has a mutation status of E125Q, The gene MAGEE1 has a mutation status of P154R, The gene ESPN has a mutation status of P452T, The gene PEX14 has a mutation status of S265L, The gene HNRNPCL2 has a mutation status of E207K, The gene EYA3 has a mutation status of V366L, The gene ZMYM6 has a mutation status of D664G, The gene NT5C1A has a mutation status of A352V, The gene SZT2 has a mutation status of A317G, The gene USP33 has a mutation status of N230Y, The gene ADGRL2 has a mutation status of W163Ter, The gene FMO5 has a mutation status of I530T, The gene GOLPH3L has a mutation status of P189S, The gene S100A10 has a mutation status of A77V, The gene SMCP has a mutation status of C65Ter, The gene MPZ has a mutation status of A83V, The gene FMO3 has a mutation status of V127A, The gene PRRC2C has a mutation status of K535R, The gene BRINP3 has a mutation status of W20R, The gene PGBD5 has a mutation status of H465Y, The gene LYST has a mutation status of L2438Q, The gene RYR2 has a mutation status of P4534H, The gene GATA3 has a mutation status of D336GfsTer17, The gene C1QL3 has a mutation status of P96S, The gene SLC39A12 has a mutation status of W446Ter, The gene ZNF22 has a mutation status of G27V, The gene WDFY4 has a mutation status of V2122L, The gene ERCC6 has a mutation status of S1099R, The gene ERCC6 has a mutation status of V83I, The gene CSTF2T has a mutation status of Q167Ter, The gene SLC25A16 has a mutation status of G299A, The gene EIF4EBP2 has a mutation status of S14R, The gene MRPS16 has a mutation status of N69K, The gene NDST2 has a mutation status of R502G, The gene LIPF has a mutation status of S134A, The gene HECTD2 has a mutation status of N86T, The gene PIK3AP1 has a mutation status of E50K, The gene PLPP4 has a mutation status of T232A, The gene LRRC27 has a mutation status of E54Ter, The gene DNHD1 has a mutation status of E4427K, The gene NELL1 has a mutation status of E417V, The gene RAG2 has a mutation status of D105N, The gene OR5D13 has a mutation status of V126E, The gene DAGLA has a mutation status of H471Y, The gene SLC22A9 has a mutation status of N107K, The gene NRXN2 has a mutation status of Q1173K, The gene CLPB has a mutation status of K10delinsNL, The gene C2CD3 has a mutation status of H2035L, The gene TPBGL has a mutation status of A247V, The gene GDPD5 has a mutation status of A353CfsTer21, The gene FAM181B has a mutation status of G306S, The gene CEP295 has a mutation status of E179V, The gene CEP126 has a mutation status of H1081Y, The gene DDX10 has a mutation status of H27R, The gene VPS11 has a mutation status of G281D, The gene C12orf4 has a mutation status of R335Q, The gene CHD4 has a mutation status of A525V, The gene ACRBP has a mutation status of F464L, The gene FAM186B has a mutation status of W566C, The gene KRT2 has a mutation status of Q161H, The gene IKZF4 has a mutation status of T19N, The gene BAZ2A has a mutation status of E621Ter, The gene BBS10 has a mutation status of G401E, The gene CFAP54 has a mutation status of L1087P, The gene HVCN1 has a mutation status of A16G, The gene ATP6V0A2 has a mutation status of S659C, The gene ADGRD1 has a mutation status of Q37H, The gene ZMYM2 has a mutation status of S289L, The gene SMAD9 has a mutation status of V42L, The gene DLEU7 has a mutation status of S129L, The gene JPH4 has a mutation status of R233C, The gene COCH has a mutation status of F527SfsTer4, The gene DACT1 has a mutation status of N372S, The gene GPR68 has a mutation status of Q95H, The gene COX8C has a mutation status of P38S, The gene PPP4R4 has a mutation status of D283Y, The gene SLC25A29 has a mutation status of P37L, The gene INF2 has a mutation status of D1239A, The gene IGHM has a mutation status of E418Q, The gene VPS18 has a mutation status of L869F, The gene ONECUT1 has a mutation status of C321Y, The gene UBAP1L has a mutation status of A124V, The gene SKOR1 has a mutation status of G307S, The gene ITGA11 has a mutation status of T593R, The gene AGBL1 has a mutation status of E167D, The gene STUB1 has a mutation status of S236G, The gene CACNA1H has a mutation status of M611I, The gene CREBBP has a mutation status of Q1967P, The gene PPL has a mutation status of E1254K, The gene ZNF778 has a mutation status of T444GfsTer8, The gene FXR2 has a mutation status of E145K, The gene LGALS9 has a mutation status of S286Y, The gene KRT32 has a mutation status of P427I, The gene HOXB7 has a mutation status of E216Ter, The gene KIF2B has a mutation status of D546N, The gene ACE has a mutation status of S233F, The gene KCNJ2 has a mutation status of L109F, The gene UNK has a mutation status of S517C, The gene QRICH2 has a mutation status of D262E, The gene CYTH1 has a mutation status of E40K, The gene CBX8 has a mutation status of S316Y, The gene PTPRM has a mutation status of D1076H, The gene SERPINB2 has a mutation status of E160Ter, The gene CDH7 has a mutation status of G198V, The gene PCSK4 has a mutation status of G302S, The gene MUC16 has a mutation status of D13719Y, The gene CPAMD8 has a mutation status of D684N, The gene GARRE1 has a mutation status of R623Ter, The gene NUMBL has a mutation status of E419Q, The gene CCDC97 has a mutation status of C136S, The gene ZNF225 has a mutation status of Q279E, The gene ZSWIM9 has a mutation status of M51T, The gene IL4I1 has a mutation status of G167D, The gene ZNF610 has a mutation status of G210C, The gene PRKCG has a mutation status of Q425Ter, The gene LAIR1 has a mutation status of A266VfsTer57, The gene EPN1 has a mutation status of E344V, The gene PEG3 has a mutation status of L434_S436del, The gene RAD51AP2 has a mutation status of D698E, The gene TDRD15 has a mutation status of G1405R, The gene BIRC6 has a mutation status of R2915K, The gene EXOC6B has a mutation status of G4A, The gene ACTG2 has a mutation status of E242K, The gene KDM3A has a mutation status of A765V, The gene CKAP2L has a mutation status of L599FfsTer14, The gene CKAP2L has a mutation status of P91Q, The gene CLASP1 has a mutation status of V1317L, The gene XIRP2 has a mutation status of I3408T, The gene RAPGEF4 has a mutation status of Y986F, The gene TTN has a mutation status of C31877S, The gene TTN has a mutation status of E19518K, The gene TTN has a mutation status of E15742D, The gene ERBB4 has a mutation status of Y1242C, The gene IRS1 has a mutation status of R327C, The gene FASTKD5 has a mutation status of I310M, The gene COX4I2 has a mutation status of A141V, The gene WDR4 has a mutation status of Q323H, The gene BCL2L13 has a mutation status of S5LfsTer40, The gene KLHL22 has a mutation status of K260N, The gene SLC5A1 has a mutation status of I397T, The gene MYH9 has a mutation status of K682_L687del, The gene CSDC2 has a mutation status of D111N, The gene UBA3 has a mutation status of A380G, The gene NECTIN3 has a mutation status of P45DfsTer13, The gene NECTIN3 has a mutation status of P45T, The gene SLC9C1 has a mutation status of L183S, The gene CD200 has a mutation status of Q102K, The gene FBXO40 has a mutation status of G337S, The gene HLTF has a mutation status of V287F, The gene STRIT1 has a mutation status of I20T, The gene TRIM59 has a mutation status of E276K, The gene TNIK has a mutation status of G884V, The gene PIK3CA has a mutation status of E545K, The gene MAP3K13 has a mutation status of D380N, The gene CLDN1 has a mutation status of Q163L, The gene MUC4 has a mutation status of T3942L, The gene MUC4 has a mutation status of L1410H, The gene WDR53 has a mutation status of A198D, The gene DGKQ has a mutation status of P935T, The gene HMX1 has a mutation status of P291T, The gene SLIT2 has a mutation status of T1221N, The gene LIAS has a mutation status of M310T, The gene ATP10D has a mutation status of Y81S, The gene EPHA5 has a mutation status of L987P, The gene TMPRSS11B has a mutation status of V56G, The gene FAM13A has a mutation status of N217K, The gene DCHS2 has a mutation status of E1201A, The gene CLCN3 has a mutation status of W555Ter, The gene ZFP42 has a mutation status of G65E, The gene ADAMTS16 has a mutation status of R1158Q, The gene MARCHF6 has a mutation status of V317F, The gene MAST4 has a mutation status of K2433Q, The gene PDE8B has a mutation status of R426Q, The gene ACOT12 has a mutation status of A403N, The gene XRCC4 has a mutation status of K197R, The gene RGMB has a mutation status of G286S, The gene SLC4A9 has a mutation status of F434I, The gene PCDHGA4 has a mutation status of Q388H, The gene JAKMIP2 has a mutation status of I265V, The gene ADAMTS2 has a mutation status of Q915K, The gene SQSTM1 has a mutation status of E101D, The gene RIPOR2 has a mutation status of Q190R, The gene ANKS1A has a mutation status of S506AfsTer80, The gene SLC26A8 has a mutation status of G964C, The gene ZFAND3 has a mutation status of R17C, The gene KIF6 has a mutation status of R600del, The gene COL9A1 has a mutation status of G364C, The gene EPHA7 has a mutation status of V418L, The gene TAAR6 has a mutation status of Y311H, The gene ALDH8A1 has a mutation status of P319S, The gene RMND1 has a mutation status of F369L, The gene SYNE1 has a mutation status of M6190I, The gene DPY19L1 has a mutation status of G84D, The gene ZNF735 has a mutation status of K183N, The gene GTF2I has a mutation status of V309IfsTer18, The gene CROT has a mutation status of T543A, The gene PDK4 has a mutation status of A144T, The gene MUC17 has a mutation status of T825N, The gene RELN has a mutation status of E2374K, The gene PLXNA4 has a mutation status of W8C, The gene ZNF467 has a mutation status of V508M, The gene GIMAP7 has a mutation status of S73R, The gene ASB10 has a mutation status of G248V, The gene MYOM2 has a mutation status of D348Y, The gene SH2D4A has a mutation status of P161T, The gene ADGRA2 has a mutation status of P434L, The gene NBN has a mutation status of R43Ter, The gene HHLA1 has a mutation status of N85S, The gene TRAPPC9 has a mutation status of L17I, The gene JRK has a mutation status of K115R, The gene CYP11B2 has a mutation status of A414P, The gene GPT has a mutation status of P472S, The gene KCNV2 has a mutation status of H26Q, The gene CCDC171 has a mutation status of E551V, The gene SHC3 has a mutation status of M1?, The gene WNK2 has a mutation status of L312Q, The gene TDRD7 has a mutation status of D962A, The gene TRMO has a mutation status of S191Y, The gene HEMGN has a mutation status of E59K, The gene NIPSNAP3B has a mutation status of N82K, The gene ELP1 has a mutation status of R1192I, The gene PTPN3 has a mutation status of M403I, The gene SVEP1 has a mutation status of A1142S, The gene AKNA has a mutation status of S1184P, The gene TTC16 has a mutation status of D373N, The gene LRRC8A has a mutation status of T170M, The gene HMCN2 has a mutation status of V2564I, The gene HMCN2 has a mutation status of I2568M, The gene PPP1R26 has a mutation status of A1185S, The gene MT-CO3 has a mutation status of V254I, The gene MT-ND6 has a mutation status of N119D, The gene MT-CYB has a mutation status of T212A, The gene FAM47A has a mutation status of W705Ter, The gene PHF8 has a mutation status of H31P, The gene ZXDA has a mutation status of Q138L, The gene MAGEE1 has a mutation status of P154R, The gene ABCD1 has a mutation status of M282T	BRCA
The gene KDM1A has a mutation status of A846V, The gene ZNF326 has a mutation status of P216L, The gene MUC6 has a mutation status of S1734PfsTer69, The gene ATG16L2 has a mutation status of A172V, The gene RHOF has a mutation status of I129L, The gene MGA has a mutation status of A2049T, The gene NF1 has a mutation status of Q535Ter, The gene DBF4B has a mutation status of P25L, The gene CACNA1G has a mutation status of A447T, The gene ABCC3 has a mutation status of D940N, The gene FBF1 has a mutation status of A919G, The gene ANGPTL6 has a mutation status of R142H, The gene CACNA1A has a mutation status of A2447D, The gene ADM5 has a mutation status of P69A, The gene PPM1B has a mutation status of E263Q, The gene EMX1 has a mutation status of C6F, The gene ABCB11 has a mutation status of D215V, The gene NEUROD1 has a mutation status of Y5F, The gene ALS2 has a mutation status of H952N, The gene RBM38 has a mutation status of R116W, The gene TAF4 has a mutation status of A354S, The gene CELSR1 has a mutation status of E2757Ter, The gene CDC25A has a mutation status of P419S, The gene GLYCTK has a mutation status of L28M, The gene IL1RAP has a mutation status of C212F, The gene ATP10D has a mutation status of K166T, The gene SHROOM3 has a mutation status of E645G, The gene ROS1 has a mutation status of I469K, The gene MUC3A has a mutation status of S2495L, The gene ZC3HAV1 has a mutation status of S724F, The gene LCN9 has a mutation status of M42V, The gene NUDT10 has a mutation status of A156G, The gene IRAK1 has a mutation status of L263M	DLBC
The gene AGRN has a mutation status of C502Ter, The gene C1orf167 has a mutation status of L299P, The gene PRAMEF12 has a mutation status of V361K, The gene PRAMEF1 has a mutation status of K275_L276delinsNM, The gene PRAMEF17 has a mutation status of R169G, The gene CROCC has a mutation status of Q929H, The gene VWA5B1 has a mutation status of A1066P, The gene ZBTB40 has a mutation status of R1026G, The gene CEP85 has a mutation status of Q385Ter, The gene FOXE3 has a mutation status of F105Y, The gene RPAP2 has a mutation status of S235L, The gene EPS8L3 has a mutation status of R464GfsTer6, The gene OR6P1 has a mutation status of A237D, The gene FCER1A has a mutation status of W203R, The gene DCAF8 has a mutation status of K374Q, The gene IGFN1 has a mutation status of P11S, The gene CHIT1 has a mutation status of S275A, The gene OR2T4 has a mutation status of C32Ter, The gene SFMBT2 has a mutation status of G132W, The gene GAD2 has a mutation status of L526F, The gene IFIT3 has a mutation status of E323D, The gene HMX3 has a mutation status of R102T, The gene MUC6 has a mutation status of A1593P, The gene TRIM68 has a mutation status of S215G, The gene SLC17A6 has a mutation status of R88C, The gene KIAA1549L has a mutation status of G126R, The gene OR5T3 has a mutation status of M23I, The gene OR8U3 has a mutation status of L185Ter, The gene TMX2 has a mutation status of K227M, The gene CBLIF has a mutation status of P125T, The gene MS4A13 has a mutation status of L113Q, The gene MS4A8 has a mutation status of V190L, The gene SLC22A8 has a mutation status of G284S, The gene GPR137 has a mutation status of G91R, The gene GRM5 has a mutation status of S440C, The gene CASP12 has a mutation status of W78C, The gene OR8B4 has a mutation status of Y148H, The gene ERC1 has a mutation status of M107I, The gene CRACR2A has a mutation status of E108V, The gene TAS2R31 has a mutation status of F233S, The gene DDX47 has a mutation status of M412I, The gene PLBD1 has a mutation status of L22RfsTer8, The gene PLBD1 has a mutation status of L21PfsTer30, The gene GYS2 has a mutation status of V88F, The gene ITPR2 has a mutation status of K225Q, The gene SLC2A13 has a mutation status of A509P, The gene MUC19 has a mutation status of R4223_D4252delextTer?, The gene DIP2B has a mutation status of E317Ter, The gene SHMT2 has a mutation status of W43C, The gene NOS1 has a mutation status of L460I, The gene LRCOL1 has a mutation status of P4L, The gene COG6 has a mutation status of M484I, The gene RPS29 has a mutation status of Y7Ter, The gene SLC8A3 has a mutation status of R5K, The gene ACOT2 has a mutation status of T185V, The gene TECPR2 has a mutation status of Q116P, The gene MTA1 has a mutation status of Y397H, The gene NPAP1 has a mutation status of H613Q, The gene SV2B has a mutation status of G22R, The gene ABCA3 has a mutation status of L1624RfsTer10, The gene ABCA3 has a mutation status of L1624M, The gene METTL22 has a mutation status of H31R, The gene AQP8 has a mutation status of G73W, The gene SEZ6L2 has a mutation status of P142S, The gene FTO has a mutation status of F114L, The gene DYNC1LI2 has a mutation status of G450D, The gene WWP2 has a mutation status of W497F, The gene VAC14 has a mutation status of V238F, The gene PER1 has a mutation status of M1231I, The gene MYH4 has a mutation status of A1636D, The gene SUZ12 has a mutation status of T438S, The gene TMEM132E has a mutation status of P280AfsTer117, The gene GAS2L2 has a mutation status of R586Q, The gene KRTAP4-16 has a mutation status of P187_P223del, The gene SNF8 has a mutation status of E123Ter, The gene COL1A1 has a mutation status of P129L, The gene DDX42 has a mutation status of Q634L, The gene ABCA5 has a mutation status of T14S, The gene CD300C has a mutation status of R215I, The gene ATP5PD has a mutation status of V67M, The gene UNC13D has a mutation status of E653Q, The gene EXOC7 has a mutation status of V308L, The gene FASN has a mutation status of P824S, The gene PIEZO2 has a mutation status of I17V, The gene FHOD3 has a mutation status of E1303Q, The gene SETBP1 has a mutation status of P1548R, The gene SALL3 has a mutation status of A185L, The gene ZNF121 has a mutation status of H354R, The gene COL5A3 has a mutation status of P1309H, The gene SMARCA4 has a mutation status of L1085QfsTer32, The gene ZNF653 has a mutation status of A225T, The gene TRIR has a mutation status of A155V, The gene AKAP8 has a mutation status of H506Q, The gene C19orf44 has a mutation status of N233TfsTer26, The gene COLGALT1 has a mutation status of S247P, The gene ZNF208 has a mutation status of P1056H, The gene ZNF607 has a mutation status of N256Y, The gene SAMD4B has a mutation status of P461A, The gene SLC1A5 has a mutation status of E253M, The gene ODAD1 has a mutation status of E354A, The gene TPO has a mutation status of G771E, The gene KIDINS220 has a mutation status of S1488R, The gene NTSR2 has a mutation status of E90D, The gene C2orf16 has a mutation status of Q2975K, The gene CLIP4 has a mutation status of Y542H, The gene ALK has a mutation status of N369K, The gene GEMIN6 has a mutation status of P124L, The gene PAIP2B has a mutation status of D78G, The gene REG1A has a mutation status of C154F, The gene CD8A has a mutation status of S158F, The gene MAL has a mutation status of H121_Y122delinsQH, The gene ANKRD36C has a mutation status of A601P, The gene KANSL3 has a mutation status of D496H, The gene TMEM131 has a mutation status of D1411E, The gene MAP4K4 has a mutation status of S990I, The gene RANBP2 has a mutation status of V1386F, The gene NCKAP5 has a mutation status of R411Ter, The gene MAP3K19 has a mutation status of S1226C, The gene ARHGAP15 has a mutation status of H349Y, The gene SCN2A has a mutation status of Q1394Ter, The gene SCN1A has a mutation status of D646Y, The gene TTN has a mutation status of L34054F, The gene CD28 has a mutation status of S80Ter, The gene PARD3B has a mutation status of R984L, The gene PIKFYVE has a mutation status of V902F, The gene IGFBP2 has a mutation status of P43RfsTer125, The gene DOCK10 has a mutation status of A1689S, The gene TEX44 has a mutation status of L383F, The gene USP40 has a mutation status of P94R, The gene UGT1A8 has a mutation status of A25T, The gene TRPM8 has a mutation status of K175N, The gene ERFE has a mutation status of R11L, The gene ASXL1 has a mutation status of L1413F, The gene TOX2 has a mutation status of P101S, The gene ARFGAP1 has a mutation status of G380C, The gene GRIK1 has a mutation status of P820H, The gene BRWD1 has a mutation status of E398D, The gene C2CD2 has a mutation status of G367R, The gene TRPM2 has a mutation status of A890E, The gene MN1 has a mutation status of G588AfsTer97, The gene XBP1 has a mutation status of M1?, The gene SEC14L4 has a mutation status of D313N, The gene CRYBG3 has a mutation status of V2350E, The gene PHLDB2 has a mutation status of R620I, The gene CD80 has a mutation status of F229Y, The gene DNAJC13 has a mutation status of K696E, The gene ZIC1 has a mutation status of R315LfsTer22, The gene MME has a mutation status of E744G, The gene WDR49 has a mutation status of G521V, The gene VPS8 has a mutation status of G1205R, The gene MUC4 has a mutation status of V3331EfsTer9, The gene MFSD10 has a mutation status of P227L, The gene C4orf50 has a mutation status of E782Q, The gene SORCS2 has a mutation status of C667Y, The gene AFF1 has a mutation status of K589AfsTer77, The gene HSD17B13 has a mutation status of A277S, The gene SPP1 has a mutation status of D307E, The gene MMRN1 has a mutation status of E719K, The gene SYNPO2 has a mutation status of T850A, The gene TMEM131L has a mutation status of F130L, The gene TENM3 has a mutation status of E379I, The gene PRDM9 has a mutation status of K423E, The gene ADAMTS12 has a mutation status of V1560L, The gene SPEF2 has a mutation status of R1115G, The gene HCN1 has a mutation status of G809C, The gene DHX29 has a mutation status of W1270Ter, The gene FAM151B has a mutation status of E111Q, The gene VCAN has a mutation status of E1783K, The gene PCDHB3 has a mutation status of A776S, The gene PCDH12 has a mutation status of S540R, The gene CSF1R has a mutation status of G714S, The gene CSF1R has a mutation status of P517T, The gene RBM22 has a mutation status of G322R, The gene FAM114A2 has a mutation status of I92V, The gene DOCK2 has a mutation status of F280L, The gene HIVEP1 has a mutation status of V334A, The gene HLA-F has a mutation status of P36T, The gene HCG22 has a mutation status of S186F, The gene CFB has a mutation status of V516A, The gene PACSIN1 has a mutation status of K51M, The gene FRS3 has a mutation status of C107Y, The gene BICRAL has a mutation status of Q877H, The gene TFAP2B has a mutation status of Q112K, The gene DDX43 has a mutation status of T205R, The gene TTK has a mutation status of Y811C, The gene SERINC1 has a mutation status of G260C, The gene GRM1 has a mutation status of P58L, The gene TULP4 has a mutation status of L631V, The gene LPA has a mutation status of G1507V, The gene ZNF316 has a mutation status of G893C, The gene VWDE has a mutation status of A784D, The gene INHBA has a mutation status of N374Y, The gene PKD1L1 has a mutation status of R1690Ter, The gene PKD1L1 has a mutation status of G253V, The gene MUC3A has a mutation status of T363M, The gene PIK3CG has a mutation status of M1039T, The gene CTTNBP2 has a mutation status of A1401D, The gene TAS2R16 has a mutation status of P44S, The gene PRRT4 has a mutation status of A773S, The gene CPA5 has a mutation status of S98Y, The gene CHCHD3 has a mutation status of D131N, The gene PRSS37 has a mutation status of Y222H, The gene EPHA1 has a mutation status of N187S, The gene GIMAP1 has a mutation status of V185A, The gene GBX1 has a mutation status of S187L, The gene CSMD1 has a mutation status of S2104R, The gene PRAG1 has a mutation status of A1237G, The gene XKR6 has a mutation status of D89Y, The gene TUSC3 has a mutation status of S267C, The gene MTMR7 has a mutation status of P20A, The gene UNC5D has a mutation status of V237M, The gene ASPH has a mutation status of C648Y, The gene KCNB2 has a mutation status of G385V, The gene KCNV1 has a mutation status of R77S, The gene CSMD3 has a mutation status of T3016N, The gene TRAPPC9 has a mutation status of R923S, The gene SLURP2 has a mutation status of T45N, The gene PYCR3 has a mutation status of R18L, The gene VLDLR has a mutation status of P647S, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of S215T, The gene RGP1 has a mutation status of W363Ter, The gene CEP78 has a mutation status of T177A, The gene PHF2 has a mutation status of R354GfsTer2, The gene DENND1A has a mutation status of R23M, The gene COL5A1 has a mutation status of P705Q, The gene QSOX2 has a mutation status of G647W, The gene TRAF2 has a mutation status of P374S, The gene MT-ND5 has a mutation status of I126T, The gene KDM5C has a mutation status of W93Ter, The gene AR has a mutation status of Y535LfsTer17, The gene OPHN1 has a mutation status of G525A, The gene ZDHHC15 has a mutation status of I270T, The gene ZDHHC15 has a mutation status of K268N, The gene PLP1 has a mutation status of K151N, The gene COL4A6 has a mutation status of G587R, The gene TEX13C has a mutation status of A175D, The gene ACTRT1 has a mutation status of C220F, The gene MAGEA12 has a mutation status of L304CfsTer37, The gene PNMA6F has a mutation status of I49L, The gene ATP2B3 has a mutation status of R199W, The gene ABCD1 has a mutation status of D685N, The gene F8 has a mutation status of L1198V	LUAD
The gene RNF223 has a mutation status of C101Ter, The gene GPR153 has a mutation status of R455H, The gene TAL1 has a mutation status of A264G, The gene TRIM33 has a mutation status of D942H, The gene FMO2 has a mutation status of R462G, The gene TMEM9 has a mutation status of R163H, The gene PKP1 has a mutation status of Y642H, The gene PLXNA2 has a mutation status of P207R, The gene PRSS38 has a mutation status of I60MfsTer35, The gene ZNF695 has a mutation status of A360T, The gene OR2M4 has a mutation status of P268S, The gene BEND7 has a mutation status of S236N, The gene YME1L1 has a mutation status of C123S, The gene MRGPRG has a mutation status of S13R, The gene MRPL11 has a mutation status of S2L, The gene GAB2 has a mutation status of R354PfsTer78, The gene MRE11 has a mutation status of R576Ter, The gene ATM has a mutation status of R919M, The gene CHEK1 has a mutation status of I124LfsTer3, The gene CD163 has a mutation status of H946Y, The gene CD69 has a mutation status of T52I, The gene KRAS has a mutation status of G12V, The gene PRICKLE1 has a mutation status of E710D, The gene KANSL2 has a mutation status of G386R, The gene MMP19 has a mutation status of S482L, The gene R3HDM2 has a mutation status of R295Q, The gene HSP90B1 has a mutation status of K410N, The gene ALDH1L2 has a mutation status of P167T, The gene HECTD4 has a mutation status of E3864K, The gene DTX1 has a mutation status of P331L, The gene MED13L has a mutation status of M1980T, The gene FZD10 has a mutation status of A72T, The gene HNRNPA1L2 has a mutation status of G248C, The gene NIN has a mutation status of I993V, The gene SIX4 has a mutation status of S615C, The gene TDRD9 has a mutation status of R1311T, The gene IGHV8-51-1 has a mutation status of L8F, The gene TYRO3 has a mutation status of F674L, The gene ZNF609 has a mutation status of D391E, The gene ROGDI has a mutation status of H24Q, The gene ATF7IP2 has a mutation status of A265E, The gene SULT1A2 has a mutation status of A164V, The gene PLD2 has a mutation status of S192I, The gene TP53 has a mutation status of R282W, The gene TNFAIP1 has a mutation status of D176Ter, The gene TNS4 has a mutation status of E85Ter, The gene BRIP1 has a mutation status of I275F, The gene CBX2 has a mutation status of K103E, The gene ANKRD30B has a mutation status of R13Q, The gene MIB1 has a mutation status of S810G, The gene RTTN has a mutation status of V964F, The gene SALL3 has a mutation status of A693T, The gene ELL has a mutation status of G11R, The gene ZNF208 has a mutation status of G365V, The gene GARRE1 has a mutation status of R941I, The gene ZNF226 has a mutation status of S376F, The gene ZNF773 has a mutation status of C221Ter, The gene DDX1 has a mutation status of E245D, The gene PCARE has a mutation status of P781S, The gene CAPN13 has a mutation status of R472Ter, The gene GALNT14 has a mutation status of T237N, The gene CFAP36 has a mutation status of N117KfsTer3, The gene ACTR1B has a mutation status of R257Q, The gene NEB has a mutation status of I7840T, The gene RAPGEF4 has a mutation status of T809I, The gene TTN has a mutation status of I30632V, The gene GPR55 has a mutation status of S134Y, The gene UGT1A10 has a mutation status of W251R, The gene SOX12 has a mutation status of Q52AfsTer50, The gene CYP24A1 has a mutation status of T265A, The gene PEX26 has a mutation status of V225I, The gene EP300 has a mutation status of C1686S, The gene TOPAZ1 has a mutation status of S746I, The gene PDZRN3 has a mutation status of R1012T, The gene PDZRN3 has a mutation status of R931C, The gene ROBO2 has a mutation status of Q1181P, The gene ARHGAP31 has a mutation status of A483V, The gene GOLGB1 has a mutation status of L331H, The gene GRK7 has a mutation status of A207P, The gene TIPARP has a mutation status of D548N, The gene MECOM has a mutation status of S1142N, The gene MUC4 has a mutation status of D2979_P3010del, The gene DGKQ has a mutation status of C149W, The gene IRF2 has a mutation status of S348C, The gene PDCD6 has a mutation status of T86M, The gene TERT has a mutation status of S656W, The gene CDH9 has a mutation status of K115NfsTer2, The gene FAM151B has a mutation status of W89Ter, The gene FTMT has a mutation status of A27T, The gene MYOT has a mutation status of W382C, The gene PCDHA10 has a mutation status of L519P, The gene PCDHA13 has a mutation status of A596T, The gene NR3C1 has a mutation status of D64H, The gene KIF4B has a mutation status of E26K, The gene EDN1 has a mutation status of I71V, The gene MCM3 has a mutation status of D460N, The gene GSTA2 has a mutation status of E168A, The gene FAM135A has a mutation status of S221P, The gene RIMS1 has a mutation status of S581R, The gene TAB2 has a mutation status of P494R, The gene AMPH has a mutation status of S599Y, The gene WDR91 has a mutation status of E403G, The gene GIMAP8 has a mutation status of I389M, The gene TMEM176B has a mutation status of E252K, The gene CHD7 has a mutation status of T2381S, The gene PEX2 has a mutation status of N26del, The gene TRPS1 has a mutation status of S213Y, The gene COL22A1 has a mutation status of L1454R, The gene PYCR3 has a mutation status of P6L, The gene RNF38 has a mutation status of V353A, The gene RNF20 has a mutation status of S544P, The gene CCDC187 has a mutation status of Q1158R, The gene MT-ND1 has a mutation status of Y30H, The gene CXorf58 has a mutation status of R205H, The gene MAGEB5 has a mutation status of W204L, The gene GNL3L has a mutation status of Q80L, The gene AMER1 has a mutation status of P456LfsTer85, The gene PRKCZ has a mutation status of Ter593SextTer11, The gene CHD5 has a mutation status of Y1524Ter, The gene CLSPN has a mutation status of M115I, The gene OMA1 has a mutation status of P473T, The gene LEPR has a mutation status of K359N, The gene LRIF1 has a mutation status of S430F, The gene TRIM33 has a mutation status of D942H, The gene SELL has a mutation status of G235W, The gene FMO2 has a mutation status of R462G, The gene LAMC2 has a mutation status of V817L, The gene DSTYK has a mutation status of S703P, The gene PLXNA2 has a mutation status of P207R, The gene PRSS38 has a mutation status of I60MfsTer35, The gene ZNF695 has a mutation status of A360T, The gene NLRP3 has a mutation status of Q183Ter, The gene BEND7 has a mutation status of S236N, The gene YME1L1 has a mutation status of C123S, The gene MRGPRG has a mutation status of S13R, The gene C11orf54 has a mutation status of V173L, The gene MRE11 has a mutation status of R576Ter, The gene TMPRSS5 has a mutation status of S65Ter, The gene NXPE4 has a mutation status of L435M, The gene CD69 has a mutation status of T52I, The gene TAS2R19 has a mutation status of L116F, The gene SLC15A5 has a mutation status of L507Ter, The gene KRAS has a mutation status of G12V, The gene MUC19 has a mutation status of R6489T, The gene KANSL2 has a mutation status of G386R, The gene KRT5 has a mutation status of G552S, The gene KERA has a mutation status of K248N, The gene HSP90B1 has a mutation status of K410N, The gene ALDH1L2 has a mutation status of P167T, The gene DTX1 has a mutation status of P331L, The gene MED13L has a mutation status of M1980T, The gene GCN1 has a mutation status of R1435P, The gene FZD10 has a mutation status of A72T, The gene TUBA3C has a mutation status of D116E, The gene GJB2 has a mutation status of M1?, The gene NIN has a mutation status of I993V, The gene SIX4 has a mutation status of S615C, The gene MOK has a mutation status of P221A, The gene TYRO3 has a mutation status of F674L, The gene C2CD4A has a mutation status of F238GfsTer86, The gene MYO9A has a mutation status of T1956S, The gene CYP1A2 has a mutation status of Q344Ter, The gene ROGDI has a mutation status of H24Q, The gene SULT1A2 has a mutation status of A164V, The gene CES5A has a mutation status of T478R, The gene CES5A has a mutation status of L25F, The gene PLD2 has a mutation status of S192I, The gene TP53 has a mutation status of R282W, The gene TNFAIP1 has a mutation status of D176Ter, The gene HNF1B has a mutation status of V375_T376delinsAP, The gene AARSD1 has a mutation status of V118L, The gene BRIP1 has a mutation status of I275F, The gene CBX2 has a mutation status of K103E, The gene MIB1 has a mutation status of S810G, The gene SALL3 has a mutation status of A693T, The gene PODNL1 has a mutation status of Q78Ter, The gene ELL has a mutation status of G11R, The gene ZNF257 has a mutation status of C126H, The gene ZNF226 has a mutation status of S376F, The gene BRSK1 has a mutation status of E166D, The gene ZNF773 has a mutation status of C221Ter, The gene ZNF132 has a mutation status of W422Ter, The gene PXDN has a mutation status of M1392T, The gene DDX1 has a mutation status of E245D, The gene ADGRF3 has a mutation status of R740L, The gene CAPN13 has a mutation status of R472Ter, The gene CFAP36 has a mutation status of N117KfsTer3, The gene ACTR1B has a mutation status of R257Q, The gene NEB has a mutation status of I7840T, The gene RAPGEF4 has a mutation status of T809I, The gene TTN has a mutation status of I30632V, The gene SCYGR2 has a mutation status of H97S, The gene UGT1A10 has a mutation status of W251R, The gene SOX12 has a mutation status of Q52AfsTer50, The gene DLGAP4 has a mutation status of S384I, The gene CYP24A1 has a mutation status of T265A, The gene PEX26 has a mutation status of V225I, The gene NGLY1 has a mutation status of I54N, The gene PDZRN3 has a mutation status of R931C, The gene ARHGAP31 has a mutation status of A483V, The gene GOLGB1 has a mutation status of C1055Y, The gene GOLGB1 has a mutation status of L331H, The gene GRK7 has a mutation status of A207P, The gene MECOM has a mutation status of S1142N, The gene MUC4 has a mutation status of A4086T, The gene DGKQ has a mutation status of C149W, The gene IRF2 has a mutation status of S348C, The gene PDCD6 has a mutation status of T86M, The gene ZNF622 has a mutation status of K192AfsTer21, The gene PELO has a mutation status of V213L, The gene MAP1B has a mutation status of S1258P, The gene IQGAP2 has a mutation status of S554IfsTer3, The gene FAM151B has a mutation status of W89Ter, The gene XRCC4 has a mutation status of A168T, The gene FTMT has a mutation status of A27T, The gene PCDHA10 has a mutation status of L519P, The gene PCDHA13 has a mutation status of A596T, The gene KIF4B has a mutation status of E26K, The gene EDN1 has a mutation status of I71V, The gene HLA-DRB5 has a mutation status of Y42H, The gene PKHD1 has a mutation status of G1651S, The gene MCM3 has a mutation status of D460N, The gene GSTA2 has a mutation status of E168A, The gene BEND6 has a mutation status of T147K, The gene FAM135A has a mutation status of S221P, The gene TAB2 has a mutation status of P494R, The gene ZNF316 has a mutation status of V53M, The gene PKD1L1 has a mutation status of G2043A, The gene AUTS2 has a mutation status of P633S, The gene TRRAP has a mutation status of A516P, The gene STAG3 has a mutation status of S1148L, The gene MUC3A has a mutation status of W18G, The gene WDR91 has a mutation status of E403G, The gene PRSS1 has a mutation status of G62A, The gene TMEM176B has a mutation status of E252K, The gene CHD7 has a mutation status of T2381S, The gene PEX2 has a mutation status of N26del, The gene TRPS1 has a mutation status of S213Y, The gene PYCR3 has a mutation status of P6L, The gene SMARCA2 has a mutation status of L946S, The gene PRSS3 has a mutation status of G208R, The gene RNF38 has a mutation status of V353A, The gene INVS has a mutation status of Q46R, The gene RNF20 has a mutation status of S544P, The gene CRB2 has a mutation status of C579F, The gene MED22 has a mutation status of L147R, The gene MT-ND1 has a mutation status of Y30H, The gene GLRA2 has a mutation status of L271F, The gene GNL3L has a mutation status of Q80L, The gene AMER1 has a mutation status of P456LfsTer85, The gene CD40LG has a mutation status of S222Y, The gene SPANXN3 has a mutation status of P16S	PAAD
The gene AGRN has a mutation status of Q960K, The gene CCDC27 has a mutation status of S53Y, The gene CAMTA1 has a mutation status of A927S, The gene PRAMEF17 has a mutation status of K346N, The gene GRIK3 has a mutation status of D100G, The gene RSPO1 has a mutation status of N224S, The gene TSPAN1 has a mutation status of E226G, The gene TUT4 has a mutation status of K364E, The gene KANK4 has a mutation status of Q513H, The gene ERICH3 has a mutation status of S693P, The gene PTGFR has a mutation status of L68R, The gene DNAI3 has a mutation status of E605Ter, The gene GBP1 has a mutation status of D479E, The gene DENND2C has a mutation status of F772L, The gene TENT5C has a mutation status of E178A, The gene SPAG17 has a mutation status of W18R, The gene ACP6 has a mutation status of E309R, The gene SPRR5 has a mutation status of P99S, The gene LAMC1 has a mutation status of N1395D, The gene LAMC2 has a mutation status of N451D, The gene CFHR5 has a mutation status of R385K, The gene ASPM has a mutation status of F1920S, The gene RNPEP has a mutation status of P8S, The gene OBSCN has a mutation status of H5338C, The gene TRIM67 has a mutation status of A141V, The gene FMN2 has a mutation status of R1340K, The gene WDR64 has a mutation status of E101Q, The gene EFCAB2 has a mutation status of I159T, The gene SPAG6 has a mutation status of A371S, The gene KIAA1217 has a mutation status of S161P, The gene ANK3 has a mutation status of R961I, The gene SUPV3L1 has a mutation status of G389V, The gene SLC29A3 has a mutation status of W68Ter, The gene MYOF has a mutation status of R1072H, The gene FBXL15 has a mutation status of G88A, The gene ADD3 has a mutation status of E623V, The gene DRD4 has a mutation status of T368SfsTer63, The gene PRR33 has a mutation status of P118R, The gene OR5J2 has a mutation status of G112S, The gene OR9Q2 has a mutation status of Q195H, The gene BAD has a mutation status of F151L, The gene PACS1 has a mutation status of E288Ter, The gene FAT3 has a mutation status of S1921I, The gene MMP13 has a mutation status of D317G, The gene SLC35F2 has a mutation status of S95L, The gene OR8B12 has a mutation status of L172P, The gene TMEM45B has a mutation status of E46Ter, The gene ANO2 has a mutation status of M90V, The gene ACRBP has a mutation status of Q293K, The gene BHLHE41 has a mutation status of P393R, The gene ERGIC2 has a mutation status of M1?, The gene CAPRIN2 has a mutation status of V916F, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene PDZRN4 has a mutation status of K769N, The gene KMT2D has a mutation status of Q3322Ter, The gene KMT2D has a mutation status of G1486D, The gene SPATS2 has a mutation status of T21N, The gene PRPF40B has a mutation status of H711N, The gene SRGAP1 has a mutation status of R937T, The gene MGAT4C has a mutation status of R99L, The gene PLXNC1 has a mutation status of V822A, The gene FAM216A has a mutation status of P190H, The gene NOS1 has a mutation status of S379F, The gene VSIG10 has a mutation status of E472K, The gene RPLP0 has a mutation status of F14LfsTer40, The gene HPD has a mutation status of P44A, The gene HIP1R has a mutation status of M804T, The gene DNAH10 has a mutation status of Y1244N, The gene GLT1D1 has a mutation status of P77T, The gene PABPC3 has a mutation status of F169L, The gene FREM2 has a mutation status of E2915V, The gene DIAPH3 has a mutation status of E937V, The gene DIS3 has a mutation status of Y121S, The gene SLITRK5 has a mutation status of E609Q, The gene ATP11A has a mutation status of T672A, The gene OR4Q2 has a mutation status of T158I, The gene KLHL33 has a mutation status of G275R, The gene TTC6 has a mutation status of S232T, The gene SPTB has a mutation status of R843W, The gene ARG2 has a mutation status of H130N, The gene AHNAK2 has a mutation status of V4424A, The gene TJP1 has a mutation status of G1219C, The gene TRPM1 has a mutation status of K1329Ter, The gene KNL1 has a mutation status of M524T, The gene PIERCE2 has a mutation status of V86L, The gene WDR24 has a mutation status of A653S, The gene ZNF205 has a mutation status of L159M, The gene PPL has a mutation status of L1219R, The gene HAPSTR1 has a mutation status of G16R, The gene GRIN2A has a mutation status of I422L, The gene PDILT has a mutation status of H437Y, The gene GTF3C1 has a mutation status of A156T, The gene KAT8 has a mutation status of L269I, The gene LONP2 has a mutation status of R562H, The gene CHD9 has a mutation status of G1234E, The gene TRADD has a mutation status of V12L, The gene EDC4 has a mutation status of S729F, The gene NFAT5 has a mutation status of N371K, The gene ADAMTS18 has a mutation status of R281G, The gene BCO1 has a mutation status of Q150K, The gene DNAAF1 has a mutation status of K286N, The gene DPEP1 has a mutation status of V199M, The gene GAS8 has a mutation status of V182F, The gene PRDM7 has a mutation status of W46Ter, The gene TP53 has a mutation status of R175H, The gene DHRS7C has a mutation status of E271Ter, The gene MYH13 has a mutation status of L1084M, The gene SCO1 has a mutation status of I257L, The gene DNAH9 has a mutation status of R4393W, The gene NCOR1 has a mutation status of Q356E, The gene RNF112 has a mutation status of R481C, The gene THRA has a mutation status of P87H, The gene KCNH4 has a mutation status of C881W, The gene NMT1 has a mutation status of N42S, The gene ACBD4 has a mutation status of S86C, The gene TOM1L1 has a mutation status of P376L, The gene PRR11 has a mutation status of V80I, The gene CHCT1 has a mutation status of G172W, The gene CACNG5 has a mutation status of Y35F, The gene MEP1B has a mutation status of G540E, The gene KLHL14 has a mutation status of L610Ter, The gene ASXL3 has a mutation status of D555A, The gene SMAD2 has a mutation status of L87R, The gene ZNF491 has a mutation status of T238I, The gene CYP4F3 has a mutation status of G417C, The gene ZNF536 has a mutation status of D581Y, The gene CHST8 has a mutation status of R9W, The gene KMT2B has a mutation status of R843Q, The gene LYPD5 has a mutation status of Y97H, The gene ZNF155 has a mutation status of I471L, The gene CEACAM16 has a mutation status of E85D, The gene RASIP1 has a mutation status of W39L, The gene ZNF845 has a mutation status of S480L, The gene ZNF765 has a mutation status of G295Ter, The gene ZNF471 has a mutation status of E145Ter, The gene ZNF470 has a mutation status of P452S, The gene ZNF416 has a mutation status of K216R, The gene NBAS has a mutation status of R136Ter, The gene APOB has a mutation status of F1480C, The gene KLHL29 has a mutation status of P264S, The gene SLC35F6 has a mutation status of W145L, The gene PLB1 has a mutation status of P1150L, The gene NLRC4 has a mutation status of D1011Y, The gene LTBP1 has a mutation status of P516L, The gene MSH6 has a mutation status of H164R, The gene PPP4R3B has a mutation status of L209H, The gene APLF has a mutation status of N227KfsTer33, The gene GPR45 has a mutation status of N4K, The gene MARCO has a mutation status of L62M, The gene CNTNAP5 has a mutation status of C592Ter, The gene RIF1 has a mutation status of S269G, The gene BAZ2B has a mutation status of P137S, The gene MARCHF7 has a mutation status of E274G, The gene ITGAV has a mutation status of Y251C, The gene FAM171B has a mutation status of I771S, The gene DNAH7 has a mutation status of I3169L, The gene CCDC150 has a mutation status of E957RfsTer23, The gene RAPH1 has a mutation status of M286I, The gene STK36 has a mutation status of D405A, The gene STK11IP has a mutation status of Q671L, The gene SLC4A3 has a mutation status of S977N, The gene CCDC195 has a mutation status of R86H, The gene INPP5D has a mutation status of P1180_P1182del, The gene COL6A3 has a mutation status of F1439L, The gene COL6A3 has a mutation status of I482N, The gene FARP2 has a mutation status of K768N, The gene VPS16 has a mutation status of A150V, The gene KAT14 has a mutation status of I293T, The gene APMAP has a mutation status of H394Q, The gene NCOA6 has a mutation status of G156A, The gene SOGA1 has a mutation status of A195T, The gene ADRM1 has a mutation status of A348V, The gene NKAIN4 has a mutation status of V162L, The gene LCA5L has a mutation status of N172S, The gene ZBTB21 has a mutation status of K547NfsTer54, The gene AIRE has a mutation status of K52E, The gene SLC25A1 has a mutation status of R118Q, The gene ZNF74 has a mutation status of E407A, The gene RFPL2 has a mutation status of T59S, The gene LARGE1 has a mutation status of R70H, The gene MCM5 has a mutation status of Y703S, The gene ELFN2 has a mutation status of H696P, The gene CARD10 has a mutation status of V875M, The gene SRGAP3 has a mutation status of Q598Ter, The gene BTD has a mutation status of T456I, The gene RFTN1 has a mutation status of Q164R, The gene ARPP21 has a mutation status of Q289H, The gene KLHL18 has a mutation status of F67L, The gene HYAL3 has a mutation status of S386N, The gene CFAP20DC has a mutation status of T192del, The gene CHMP2B has a mutation status of A77S, The gene ZPLD1 has a mutation status of P147QfsTer3, The gene GPR156 has a mutation status of F70L, The gene HEG1 has a mutation status of R1217Ter, The gene ISY1 has a mutation status of G51E, The gene ARHGEF26 has a mutation status of R426Ter, The gene GPR149 has a mutation status of V154A, The gene BCHE has a mutation status of K596E, The gene FXR1 has a mutation status of H208Y, The gene MUC4 has a mutation status of T3942L, The gene FGFR3 has a mutation status of K650E, The gene ADD1 has a mutation status of V183F, The gene KLB has a mutation status of A672V, The gene ZAR1 has a mutation status of R174L, The gene ERVMER34-1 has a mutation status of P429Q, The gene SLC4A4 has a mutation status of V138L, The gene RCHY1 has a mutation status of R15Q, The gene ODAPH has a mutation status of P117T, The gene CDKL2 has a mutation status of E294G, The gene CDS1 has a mutation status of N388T, The gene ARHGAP24 has a mutation status of R175Ter, The gene FAT4 has a mutation status of K4214E, The gene LRBA has a mutation status of R167C, The gene SFRP2 has a mutation status of P101T, The gene GALNTL6 has a mutation status of R3del, The gene SLC9A3 has a mutation status of I384V, The gene TAS2R1 has a mutation status of T211A, The gene TRIO has a mutation status of F124L, The gene SKP2 has a mutation status of D301G, The gene CDC20B has a mutation status of A148E, The gene MTREX has a mutation status of S11G, The gene PDE4D has a mutation status of I212T, The gene MCTP1 has a mutation status of L88V, The gene FBN2 has a mutation status of V407F, The gene SPOCK1 has a mutation status of N298T, The gene PCDHB3 has a mutation status of Y751C, The gene PCDHB6 has a mutation status of R788W, The gene PCDHGA6 has a mutation status of N145T, The gene NMUR2 has a mutation status of V341G, The gene GFPT2 has a mutation status of E534D, The gene TXNDC5 has a mutation status of P348L, The gene TMEM170B has a mutation status of G101V, The gene KIF13A has a mutation status of L458F, The gene OR2J1 has a mutation status of P59L, The gene OR2J3 has a mutation status of V225F, The gene HLA-DQA2 has a mutation status of S75R, The gene TCTE1 has a mutation status of T6M, The gene COL9A1 has a mutation status of K126N, The gene GJB7 has a mutation status of A96V, The gene STXBP5 has a mutation status of K895E, The gene INTS1 has a mutation status of H1873P, The gene HOXA13 has a mutation status of Y290Ter, The gene AEBP1 has a mutation status of I817F, The gene ERVW-1 has a mutation status of L333Ter, The gene FAM200A has a mutation status of K262N, The gene CYP3A43 has a mutation status of F203L, The gene MUC3A has a mutation status of T289M, The gene MGAM2 has a mutation status of L337P, The gene MGAM2 has a mutation status of T1941I, The gene NOBOX has a mutation status of P333A, The gene DLGAP2 has a mutation status of H234Y, The gene DLGAP2 has a mutation status of V856I, The gene KBTBD11 has a mutation status of A86G, The gene HTRA4 has a mutation status of L22F, The gene KCNB2 has a mutation status of M344T, The gene RUNX1T1 has a mutation status of D406E, The gene HAS2 has a mutation status of M444L, The gene PLEC has a mutation status of R753C, The gene OPLAH has a mutation status of F1201L, The gene DGAT1 has a mutation status of R280Q, The gene PLPP6 has a mutation status of A102T, The gene FOCAD has a mutation status of E578G, The gene CDKN2A has a mutation status of H83Y, The gene UNC13B has a mutation status of D1708E, The gene DAPK1 has a mutation status of R48del, The gene DAPK1 has a mutation status of H1359N, The gene DIRAS2 has a mutation status of K108R, The gene PHF19 has a mutation status of A452S, The gene SH2D3C has a mutation status of V607I, The gene HMCN2 has a mutation status of C1460S, The gene AIF1L has a mutation status of K121M, The gene EXD3 has a mutation status of G294W, The gene MT-ND1 has a mutation status of A64V, The gene MT-ND6 has a mutation status of T156I, The gene EIF1AX has a mutation status of R62G, The gene IL1RAPL1 has a mutation status of P177S, The gene FAM47C has a mutation status of D56Y, The gene XAGE2 has a mutation status of T76I, The gene NLGN3 has a mutation status of P780S, The gene ERCC6L has a mutation status of E978Q, The gene ATP7A has a mutation status of S1417I, The gene NXF3 has a mutation status of D310V	DLBC
The gene NRAS has a mutation status of Q61K, The gene CFHR5 has a mutation status of P282Q, The gene RAB3GAP2 has a mutation status of T1232A, The gene PTEN has a mutation status of L57WfsTer42, The gene MUC6 has a mutation status of P2398S, The gene USP47 has a mutation status of S478N, The gene ACP2 has a mutation status of A224T, The gene FAM181B has a mutation status of W414R, The gene REXO2 has a mutation status of H163R, The gene BCL2L14 has a mutation status of P40A, The gene LRRIQ1 has a mutation status of V427L, The gene HSPH1 has a mutation status of R196Q, The gene WBP4 has a mutation status of S62P, The gene AHNAK2 has a mutation status of N2143D, The gene AHNAK2 has a mutation status of D1352CfsTer10, The gene IQCH has a mutation status of I175M, The gene ANP32A has a mutation status of K62R, The gene NR2F2 has a mutation status of C99R, The gene DNAH3 has a mutation status of C902R, The gene HS3ST2 has a mutation status of R196Ter, The gene TNRC6A has a mutation status of P115_Q119del, The gene SPNS2 has a mutation status of Q144H, The gene SLC2A4 has a mutation status of E375G, The gene CTC1 has a mutation status of D893N, The gene ASIC2 has a mutation status of L456R, The gene TBX2 has a mutation status of K432R, The gene BRIP1 has a mutation status of C350S, The gene FSD1 has a mutation status of A41P, The gene ZNF146 has a mutation status of E145D, The gene ZNF607 has a mutation status of R74S, The gene NLRP7 has a mutation status of C645G, The gene LRP1B has a mutation status of I4387M, The gene CHGB has a mutation status of E233A, The gene PLCB4 has a mutation status of N301D, The gene KRTAP23-1 has a mutation status of G63E, The gene TBX1 has a mutation status of R289Q, The gene IGLV5-45 has a mutation status of A95T, The gene IGLV5-45 has a mutation status of I99L, The gene KIAA0930 has a mutation status of S206F, The gene ZDHHC3 has a mutation status of A140V, The gene BSN has a mutation status of P85L, The gene CHCHD6 has a mutation status of R61K, The gene MUC4 has a mutation status of V1070_T1086delinsA, The gene ATP8A1 has a mutation status of Y70Ter, The gene C4orf54 has a mutation status of K1431T, The gene MFAP3L has a mutation status of P76S, The gene CYP4V2 has a mutation status of F488V, The gene RIPOR2 has a mutation status of Q736Ter, The gene TUBB has a mutation status of R282Q, The gene HLA-DRB1 has a mutation status of T106N, The gene HLA-DRB1 has a mutation status of W38E, The gene C1GALT1 has a mutation status of F65L, The gene MGAM has a mutation status of N438K, The gene KMT2C has a mutation status of T1904I, The gene ST18 has a mutation status of K227T, The gene SLC44A1 has a mutation status of R16G, The gene SETX has a mutation status of F2339Y, The gene LONRF3 has a mutation status of L272M	GBMLGG
The gene PRAMEF12 has a mutation status of T199IfsTer8, The gene ARID1A has a mutation status of G91C, The gene S100PBP has a mutation status of L326H, The gene CELSR2 has a mutation status of R2015K, The gene AP4B1 has a mutation status of V335A, The gene TARS2 has a mutation status of R684W, The gene BRINP3 has a mutation status of D249N, The gene COX20 has a mutation status of F66Y, The gene PTEN has a mutation status of C124S, The gene MUC5B has a mutation status of W1905R, The gene HPS5 has a mutation status of S243Y, The gene OR6Q1 has a mutation status of F242L, The gene OVOL1 has a mutation status of R166Ter, The gene BIRC2 has a mutation status of K38T, The gene ZNF202 has a mutation status of Q173H, The gene ZNF202 has a mutation status of T170I, The gene ARHGAP32 has a mutation status of T1084I, The gene CACNA1C has a mutation status of T568M, The gene GALNT6 has a mutation status of S458H, The gene ANKRD52 has a mutation status of R321C, The gene EEA1 has a mutation status of M449R, The gene CFAP54 has a mutation status of L2508V, The gene TMPO has a mutation status of L375V, The gene REM2 has a mutation status of V339G, The gene HEATR5A has a mutation status of A1687QfsTer10, The gene HEATR5A has a mutation status of D902Y, The gene HERC2 has a mutation status of S3789L, The gene C2CD4A has a mutation status of P94Q, The gene UMOD has a mutation status of S301N, The gene LCAT has a mutation status of A235G, The gene ATMIN has a mutation status of E499GfsTer6, The gene ATMIN has a mutation status of E499DfsTer7, The gene DNAH2 has a mutation status of Q2807Ter, The gene GLP2R has a mutation status of W524CfsTer45, The gene ALKBH5 has a mutation status of R11L, The gene KRT17 has a mutation status of E332_N333delinsDY, The gene METRNL has a mutation status of G149S, The gene USP14 has a mutation status of V18I, The gene APC2 has a mutation status of G1447D, The gene ZNF729 has a mutation status of C908S, The gene NOP53 has a mutation status of L279M, The gene TRPM4 has a mutation status of Y859F, The gene ZNF611 has a mutation status of R605Q, The gene NLRP9 has a mutation status of P43L, The gene ZNF749 has a mutation status of C206S, The gene PCARE has a mutation status of S854F, The gene CCDC85A has a mutation status of E76K, The gene ACVR1C has a mutation status of V434F, The gene ACVR1C has a mutation status of R432Ter, The gene FZD5 has a mutation status of R269C, The gene TRIB3 has a mutation status of K184M, The gene PAX1 has a mutation status of P233S, The gene ASXL1 has a mutation status of R411L, The gene MICAL3 has a mutation status of S1700P, The gene MICAL3 has a mutation status of R745W, The gene GNB1L has a mutation status of D306V, The gene NF2 has a mutation status of P181RfsTer28, The gene IQSEC1 has a mutation status of V824del, The gene DNAH1 has a mutation status of F2489L, The gene OR5K4 has a mutation status of L166Ter, The gene EPHB1 has a mutation status of P207S, The gene B3GALNT1 has a mutation status of H40R, The gene SERPINI1 has a mutation status of K318R, The gene NAALADL2 has a mutation status of N295KfsTer19, The gene CLDN1 has a mutation status of P154S, The gene MFSD10 has a mutation status of T292K, The gene GABRB1 has a mutation status of P59S, The gene ADAMTS3 has a mutation status of G682Ter, The gene SHROOM3 has a mutation status of P878R, The gene CENPE has a mutation status of E830G, The gene MCUB has a mutation status of R184I, The gene PLRG1 has a mutation status of L108F, The gene PALLD has a mutation status of E196Q, The gene CDH12 has a mutation status of I330T, The gene IQGAP2 has a mutation status of Q953R, The gene SLC12A2 has a mutation status of A642T, The gene NRG2 has a mutation status of V182L, The gene NRG2 has a mutation status of S102P, The gene NRG2 has a mutation status of P97S, The gene PCDHA8 has a mutation status of R98W, The gene SLC36A1 has a mutation status of G96S, The gene GARIN3 has a mutation status of A314T, The gene BLOC1S5 has a mutation status of A175P, The gene SLC17A2 has a mutation status of I115K, The gene FILIP1 has a mutation status of S12F, The gene MRAP2 has a mutation status of R160S, The gene ASCC3 has a mutation status of G1401V, The gene SLC22A16 has a mutation status of W366Ter, The gene MARCKS has a mutation status of S6Y, The gene ZNF12 has a mutation status of S412N, The gene GLI3 has a mutation status of H1353N, The gene EGFR has a mutation status of D256G, The gene KMT2C has a mutation status of P2051R, The gene CNGB3 has a mutation status of F432S, The gene RGS22 has a mutation status of M1?, The gene TRPM6 has a mutation status of E799D, The gene AOPEP has a mutation status of D204H, The gene PGAP4 has a mutation status of R231C, The gene NOTCH1 has a mutation status of C423W, The gene FAM104B has a mutation status of T22N, The gene FHL1 has a mutation status of A53G, The gene PRAMEF12 has a mutation status of T199IfsTer8, The gene C1QB has a mutation status of D248H, The gene S100PBP has a mutation status of L326H, The gene TFAP2E has a mutation status of D362H, The gene FPGT has a mutation status of I583M, The gene CELSR2 has a mutation status of R2015K, The gene AP4B1 has a mutation status of V335A, The gene TARS2 has a mutation status of R684W, The gene FLG has a mutation status of A892K, The gene PBXIP1 has a mutation status of R650L, The gene OR10Z1 has a mutation status of F12S, The gene CADM3 has a mutation status of S98T, The gene OR10J5 has a mutation status of V303L, The gene IGFN1 has a mutation status of G2743C, The gene COX20 has a mutation status of F66Y, The gene PTER has a mutation status of G6Ter, The gene PTEN has a mutation status of C124S, The gene FFAR4 has a mutation status of A154S, The gene PDZD7 has a mutation status of V169L, The gene PNLIPRP1 has a mutation status of F10L, The gene KCNK18 has a mutation status of T322S, The gene FGFR2 has a mutation status of S252L, The gene MUC5AC has a mutation status of S2573I, The gene UBQLN3 has a mutation status of Q526H, The gene MICAL2 has a mutation status of S1945R, The gene OVOL1 has a mutation status of R166Ter, The gene USP28 has a mutation status of D1118G, The gene TMPRSS13 has a mutation status of S427F, The gene PANX3 has a mutation status of L266P, The gene ALG10B has a mutation status of P409S, The gene KRT85 has a mutation status of S316R, The gene KRT76 has a mutation status of G130C, The gene E2F7 has a mutation status of D244AfsTer2, The gene MYF6 has a mutation status of R101C, The gene CFAP54 has a mutation status of L2508V, The gene TMPO has a mutation status of L375V, The gene LACC1 has a mutation status of R230C, The gene OLFM4 has a mutation status of P239H, The gene MYCBP2 has a mutation status of Q1872K, The gene ARMH4 has a mutation status of D253N, The gene IGHV4-39 has a mutation status of E42Q, The gene TUBGCP5 has a mutation status of K988Q, The gene MAGEL2 has a mutation status of P567L, The gene OTUD7A has a mutation status of T10P, The gene FMN1 has a mutation status of T822A, The gene RYR3 has a mutation status of R1100Q, The gene CGNL1 has a mutation status of S89R, The gene AP3B2 has a mutation status of T556I, The gene AP3B2 has a mutation status of G441C, The gene PPL has a mutation status of Q1726Ter, The gene UMOD has a mutation status of S301N, The gene CDH16 has a mutation status of D681N, The gene FCSK has a mutation status of G381W, The gene ATMIN has a mutation status of E499GfsTer6, The gene ATMIN has a mutation status of E499DfsTer7, The gene TEKT1 has a mutation status of N233S, The gene SOX15 has a mutation status of A19T, The gene EFCAB5 has a mutation status of A633D, The gene TMEM132E has a mutation status of E777K, The gene KRT39 has a mutation status of K156M, The gene HCRT has a mutation status of A124V, The gene STXBP4 has a mutation status of E277G, The gene SCN4A has a mutation status of R282C, The gene USP14 has a mutation status of V18I, The gene CABLES1 has a mutation status of A18T, The gene SETBP1 has a mutation status of L1538P, The gene CDH20 has a mutation status of I242TfsTer13, The gene MUC16 has a mutation status of T9907A, The gene KRI1 has a mutation status of A344_K351del, The gene ZNF626 has a mutation status of I495H, The gene ZNF729 has a mutation status of C908S, The gene PLEKHG2 has a mutation status of D1046H, The gene ZNF222 has a mutation status of C439Y, The gene SYT3 has a mutation status of E6D, The gene ZNF611 has a mutation status of R605Q, The gene NLRP9 has a mutation status of P43L, The gene PEG3 has a mutation status of E1279D, The gene ZNF749 has a mutation status of C206S, The gene PCARE has a mutation status of S854F, The gene VAX2 has a mutation status of G4W, The gene ST6GAL2 has a mutation status of P85H, The gene AMER3 has a mutation status of T626I, The gene ACVR1C has a mutation status of L31R, The gene CCDC148 has a mutation status of Q30Ter, The gene SCN3A has a mutation status of T235A, The gene MYO3B has a mutation status of V1137F, The gene TMEM198 has a mutation status of V238M, The gene TRIB3 has a mutation status of K184M, The gene RALGAPA2 has a mutation status of A341V, The gene E2F1 has a mutation status of A52_P58del, The gene SYCP2 has a mutation status of H612Q, The gene DYRK1A has a mutation status of G616S, The gene ABCG1 has a mutation status of R627Q, The gene MICAL3 has a mutation status of R745W, The gene SCUBE1 has a mutation status of N248H, The gene ARSA has a mutation status of G357S, The gene FGD5 has a mutation status of A425S, The gene TRANK1 has a mutation status of V1886G, The gene LTF has a mutation status of P303Q, The gene DNAH1 has a mutation status of F2489L, The gene CRYBG3 has a mutation status of P95S, The gene OR5K4 has a mutation status of L166Ter, The gene SLCO2A1 has a mutation status of L40I, The gene EPHB1 has a mutation status of P207S, The gene VEPH1 has a mutation status of P763S, The gene SERPINI1 has a mutation status of K318R, The gene NAALADL2 has a mutation status of N295KfsTer19, The gene ADIPOQ has a mutation status of A88D, The gene CLDN1 has a mutation status of P154S, The gene MUC4 has a mutation status of L1410H, The gene TMEM175 has a mutation status of I150T, The gene EVC2 has a mutation status of R426G, The gene GNPDA2 has a mutation status of K50NfsTer7, The gene ADAMTS3 has a mutation status of G682Ter, The gene SHROOM3 has a mutation status of P878R, The gene PALLD has a mutation status of E196Q, The gene CCDC110 has a mutation status of S126F, The gene CDH12 has a mutation status of I330T, The gene IQGAP2 has a mutation status of Q953R, The gene ZFYVE16 has a mutation status of E225G, The gene NRG2 has a mutation status of V182L, The gene PCDHA9 has a mutation status of T390R, The gene PCDHGA8 has a mutation status of G624C, The gene GARIN3 has a mutation status of A314T, The gene GABRA6 has a mutation status of K122E, The gene RNF44 has a mutation status of H174Y, The gene EDN1 has a mutation status of G145EfsTer16, The gene SLC17A2 has a mutation status of I115K, The gene NOTCH4 has a mutation status of C359S, The gene MRAP2 has a mutation status of R160S, The gene ASCC3 has a mutation status of G1401V, The gene SLC22A16 has a mutation status of W366Ter, The gene SYNE1 has a mutation status of F2809S, The gene ZNF12 has a mutation status of S412N, The gene ICA1 has a mutation status of I38V, The gene ABCA13 has a mutation status of L4235P, The gene MLXIPL has a mutation status of E610Ter, The gene STEAP2 has a mutation status of H55Y, The gene ZNF394 has a mutation status of K384E, The gene MGAM2 has a mutation status of A1224E, The gene CSMD1 has a mutation status of H2826Q, The gene CHD7 has a mutation status of W1994C, The gene TRPM6 has a mutation status of W1397R, The gene PGAP4 has a mutation status of R231C, The gene SPTAN1 has a mutation status of L491F, The gene OFD1 has a mutation status of S5F, The gene UXT has a mutation status of D40V, The gene ZXDA has a mutation status of Q138L, The gene SYTL4 has a mutation status of S155F, The gene TEX13C has a mutation status of Q803H, The gene MAGEC1 has a mutation status of P379H, The gene CLIC2 has a mutation status of N48I, The gene VAMP7 has a mutation status of K84N	GBMLGG
The gene MMEL1 has a mutation status of W206G, The gene HSPG2 has a mutation status of R2730I, The gene TFAP2E has a mutation status of P56RfsTer122, The gene AGO1 has a mutation status of L678R, The gene CFAP57 has a mutation status of S1241C, The gene MROH7 has a mutation status of S477C, The gene LRRC7 has a mutation status of Q1234E, The gene FPGT has a mutation status of S591N, The gene COL24A1 has a mutation status of F121I, The gene DNTTIP2 has a mutation status of R272K, The gene PRMT6 has a mutation status of R274H, The gene CELSR2 has a mutation status of A158E, The gene FLG has a mutation status of W1934C, The gene SPTA1 has a mutation status of G1882Ter, The gene SLAMF6 has a mutation status of L124EfsTer24, The gene MAEL has a mutation status of D425Y, The gene FMO3 has a mutation status of V110L, The gene CFHR1 has a mutation status of S204C, The gene USH2A has a mutation status of K3397T, The gene GNPAT has a mutation status of G460R, The gene NID1 has a mutation status of T725I, The gene ZP4 has a mutation status of G80D, The gene OR2G3 has a mutation status of L276V, The gene MALRD1 has a mutation status of D1753N, The gene DNAJC1 has a mutation status of P21R, The gene ACBD5 has a mutation status of A22P, The gene ZNF33B has a mutation status of H407Y, The gene ZNF365 has a mutation status of N390KfsTer16, The gene PALD1 has a mutation status of V509M, The gene POLR3A has a mutation status of I1117KfsTer23, The gene POLR3A has a mutation status of Y550C, The gene WAPL has a mutation status of G340R, The gene PLCE1 has a mutation status of E1354Ter, The gene C10orf95 has a mutation status of E51D, The gene FAM24A has a mutation status of I11V, The gene MUC6 has a mutation status of A1593P, The gene OTOG has a mutation status of Y977S, The gene PTPN5 has a mutation status of V234I, The gene SLC5A12 has a mutation status of Q257Ter, The gene OR5I1 has a mutation status of N91K, The gene OR8K5 has a mutation status of R20L, The gene MS4A8 has a mutation status of N56T, The gene C2CD3 has a mutation status of L1437_Y1439del, The gene TPBGL has a mutation status of A143T, The gene FAT3 has a mutation status of D2262Y, The gene ZBTB16 has a mutation status of R566H, The gene ZPR1 has a mutation status of P12RfsTer41, The gene TBRG1 has a mutation status of L366F, The gene VWF has a mutation status of G142S, The gene PRH2 has a mutation status of Q161K, The gene BCAT1 has a mutation status of W267Ter, The gene MUC19 has a mutation status of V2339G, The gene MUC19 has a mutation status of V3742M, The gene KRT85 has a mutation status of R16S, The gene KIF5A has a mutation status of Y936Ter, The gene MYBPC1 has a mutation status of I769T, The gene ISCU has a mutation status of R8C, The gene SELPLG has a mutation status of E361Ter, The gene MAPKAPK5 has a mutation status of I273M, The gene OAS2 has a mutation status of L311P, The gene GCN1 has a mutation status of A1525V, The gene HIP1R has a mutation status of E308A, The gene FRY has a mutation status of V341M, The gene DACH1 has a mutation status of R650Q, The gene CCDC168 has a mutation status of A5113T, The gene SALL2 has a mutation status of G405R, The gene TOGARAM1 has a mutation status of D35G, The gene FANCM has a mutation status of L1785V, The gene STYX has a mutation status of R97C, The gene DNAL1 has a mutation status of V148L, The gene TTLL5 has a mutation status of Q1157K, The gene MARK3 has a mutation status of I622M, The gene IGHV4-59 has a mutation status of E35Q, The gene SEMA6D has a mutation status of N107K, The gene BCL2L10 has a mutation status of L27V, The gene VPS13C has a mutation status of F3261V, The gene ZSCAN2 has a mutation status of E155D, The gene MAN2A2 has a mutation status of T79K, The gene UBN1 has a mutation status of D207H, The gene ABAT has a mutation status of Q264R, The gene PRR14 has a mutation status of A540T, The gene CCDC102A has a mutation status of A275V, The gene WWP2 has a mutation status of G344A, The gene ANKRD11 has a mutation status of Q1176K, The gene ANKRD11 has a mutation status of C1130Ter, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene TP53 has a mutation status of R248Q, The gene USP43 has a mutation status of L344R, The gene MYH8 has a mutation status of K1531E, The gene DNAH9 has a mutation status of Q1951Ter, The gene RAPGEFL1 has a mutation status of L234P, The gene BCAS3 has a mutation status of P519S, The gene CBX2 has a mutation status of S459N, The gene ZBTB7A has a mutation status of T94M, The gene CHAF1A has a mutation status of R336T, The gene PRAM1 has a mutation status of C658Y, The gene ZNF414 has a mutation status of A312GfsTer28, The gene ZNF414 has a mutation status of A311G, The gene S1PR2 has a mutation status of T320I, The gene TMEM205 has a mutation status of G8A, The gene ZNF729 has a mutation status of M1036I, The gene ZNF730 has a mutation status of I445M, The gene SPRED3 has a mutation status of W215G, The gene ZNF546 has a mutation status of T265I, The gene ATP1A3 has a mutation status of K81M, The gene ZNF404 has a mutation status of H433N, The gene ZNF112 has a mutation status of L455FfsTer3, The gene RSPH6A has a mutation status of M271R, The gene PTGIR has a mutation status of F295C, The gene CABP5 has a mutation status of I70_L72del, The gene HAS1 has a mutation status of H397Q, The gene ZNF331 has a mutation status of W32L, The gene LILRB3 has a mutation status of W205Q, The gene NLRP2 has a mutation status of S179R, The gene SBK3 has a mutation status of D273Y, The gene MYT1L has a mutation status of A970V, The gene PUM2 has a mutation status of A484P, The gene APOB has a mutation status of C2933F, The gene ITSN2 has a mutation status of Q725L, The gene PEX13 has a mutation status of P235S, The gene IGKV1-5 has a mutation status of T32N, The gene DPP10 has a mutation status of Y655C, The gene TTLL4 has a mutation status of S1143F, The gene UGT1A5 has a mutation status of L132M, The gene HDLBP has a mutation status of R534H, The gene XRN2 has a mutation status of I208T, The gene THBD has a mutation status of T411I, The gene NCOA3 has a mutation status of P261S, The gene PREX1 has a mutation status of E1135D, The gene APCDD1L has a mutation status of L221V, The gene PHACTR3 has a mutation status of K110N, The gene DIDO1 has a mutation status of P1918L, The gene COL20A1 has a mutation status of Q601RfsTer38, The gene PCMTD2 has a mutation status of D37Y, The gene JAM2 has a mutation status of S112I, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene RFPL3 has a mutation status of L151C, The gene IL2RB has a mutation status of T476M, The gene ZC3H7B has a mutation status of F585L, The gene TAFA5 has a mutation status of G43V, The gene IL17RE has a mutation status of M117I, The gene FANCD2OS has a mutation status of D122H, The gene SLC6A6 has a mutation status of D32G, The gene KCNH8 has a mutation status of E839V, The gene ZNF385D has a mutation status of S352N, The gene GOLGA4 has a mutation status of S185L, The gene CSRNP1 has a mutation status of Q260R, The gene TWF2 has a mutation status of S349I, The gene PBRM1 has a mutation status of A1249T, The gene OR5H1 has a mutation status of I158F, The gene OR5H15 has a mutation status of G161R, The gene DPPA2 has a mutation status of C96Y, The gene MYLK has a mutation status of Y1353S, The gene PODXL2 has a mutation status of P325H, The gene RHO has a mutation status of P327T, The gene IFT80 has a mutation status of M412T, The gene YEATS2 has a mutation status of E60D, The gene OPA1 has a mutation status of M610T, The gene SEL1L3 has a mutation status of L519M, The gene RBPJ has a mutation status of S452A, The gene DTHD1 has a mutation status of E595G, The gene SHROOM3 has a mutation status of S1599Y, The gene PAPSS1 has a mutation status of M496L, The gene USP38 has a mutation status of T584_K588del, The gene DCLK2 has a mutation status of A737G, The gene FGA has a mutation status of S364R, The gene HMGCS1 has a mutation status of G122R, The gene DDX4 has a mutation status of S113C, The gene MAST4 has a mutation status of V1444M, The gene ANKRD31 has a mutation status of R606G, The gene CERT1 has a mutation status of V453I, The gene VCAN has a mutation status of S1315G, The gene LYSMD3 has a mutation status of A221V, The gene ADRB2 has a mutation status of R259C, The gene FAT2 has a mutation status of R3649L, The gene FARS2 has a mutation status of Y113C, The gene E2F3 has a mutation status of L98F, The gene PRRC2A has a mutation status of R853H, The gene CLIC1 has a mutation status of A98T, The gene C6orf132 has a mutation status of P989L, The gene RUNX2 has a mutation status of R426S, The gene IL17A has a mutation status of P31T, The gene CEP162 has a mutation status of E85IfsTer3, The gene MDN1 has a mutation status of R5570L, The gene CASP8AP2 has a mutation status of R1836G, The gene AK9 has a mutation status of S1357G, The gene RSPH4A has a mutation status of E517D, The gene ADGB has a mutation status of V841I, The gene RGS17 has a mutation status of M61L, The gene ELFN1 has a mutation status of A796T, The gene EGFR has a mutation status of E746_A750del, The gene MUC3A has a mutation status of W18G, The gene ZNF800 has a mutation status of H504IfsTer23, The gene WDR91 has a mutation status of R75H, The gene NUP205 has a mutation status of E700Q, The gene SLC37A3 has a mutation status of L415P, The gene PTPRN2 has a mutation status of S208Y, The gene INTS10 has a mutation status of L348H, The gene SULF1 has a mutation status of G529E, The gene HNF4G has a mutation status of W347C, The gene BAALC has a mutation status of A35S, The gene TNFRSF11B has a mutation status of G129EfsTer45, The gene COL14A1 has a mutation status of V930I, The gene ZFAT has a mutation status of G740R, The gene CPSF1 has a mutation status of A644D, The gene CDKN2A has a mutation status of G67V, The gene CNTFR has a mutation status of S294C, The gene NMRK1 has a mutation status of E42D, The gene SPATA31D1 has a mutation status of D183N, The gene IARS1 has a mutation status of P437L, The gene ZNF510 has a mutation status of E59D, The gene FRRS1L has a mutation status of G48E, The gene DOLPP1 has a mutation status of L120Ter, The gene CCDC183 has a mutation status of L334R, The gene MT-ND1 has a mutation status of G29S, The gene MT-CYB has a mutation status of A354T, The gene AKAP17A has a mutation status of S610N, The gene CTPS2 has a mutation status of R103C, The gene CFAP47 has a mutation status of K598I, The gene ITIH6 has a mutation status of Y1190H, The gene FOXR2 has a mutation status of S135C, The gene AMER1 has a mutation status of H879P, The gene IL13RA2 has a mutation status of P241S, The gene LAMP2 has a mutation status of C153Y, The gene CCDC160 has a mutation status of S27Y, The gene ZNF449 has a mutation status of G419E, The gene CNGA2 has a mutation status of P433S, The gene KLHL21 has a mutation status of A285S, The gene KLHDC7A has a mutation status of G589R, The gene HSPG2 has a mutation status of R2730I, The gene RNF19B has a mutation status of S560Ter, The gene TFAP2E has a mutation status of P56RfsTer122, The gene CCDC30 has a mutation status of R289Q, The gene CFAP57 has a mutation status of S1241C, The gene SLC5A9 has a mutation status of I192L, The gene MROH7 has a mutation status of S477C, The gene LRRC7 has a mutation status of Q1234E, The gene FPGT has a mutation status of S591N, The gene SPATA1 has a mutation status of E95K, The gene COL24A1 has a mutation status of F121I, The gene DNTTIP2 has a mutation status of R272K, The gene ARHGAP29 has a mutation status of K12T, The gene CELSR2 has a mutation status of A158E, The gene CELSR2 has a mutation status of Q398L, The gene SPAG17 has a mutation status of A2177E, The gene FLG has a mutation status of W1934C, The gene PRR9 has a mutation status of E63Ter, The gene UBAP2L has a mutation status of R151L, The gene HAX1 has a mutation status of P198Q, The gene PEAR1 has a mutation status of P651T, The gene OR6N1 has a mutation status of A237V, The gene AIM2 has a mutation status of A339E, The gene KCNJ9 has a mutation status of E277D, The gene NHLH1 has a mutation status of R46Q, The gene SLAMF6 has a mutation status of L124EfsTer24, The gene RXRG has a mutation status of Q322K, The gene FMO3 has a mutation status of V110L, The gene CEP350 has a mutation status of E1121K, The gene CACNA1E has a mutation status of F1426L, The gene C1orf21 has a mutation status of K20N, The gene RGS2 has a mutation status of Q203K, The gene USH2A has a mutation status of T3829I, The gene USH2A has a mutation status of K3397T, The gene USH2A has a mutation status of G2269A, The gene GNPAT has a mutation status of G460R, The gene NID1 has a mutation status of T725I, The gene RYR2 has a mutation status of Q1123K, The gene ZP4 has a mutation status of G80D, The gene MALRD1 has a mutation status of D1753N, The gene DNAJC1 has a mutation status of P21R, The gene GAD2 has a mutation status of E158Ter, The gene MASTL has a mutation status of S597F, The gene ACBD5 has a mutation status of A22P, The gene PTCHD3 has a mutation status of I682_E684delinsK, The gene MPP7 has a mutation status of K105N, The gene ITGB1 has a mutation status of I334F, The gene ZNF33B has a mutation status of H407Y, The gene RASGEF1A has a mutation status of V217M, The gene BICC1 has a mutation status of D692N, The gene ZNF365 has a mutation status of N390KfsTer16, The gene HERC4 has a mutation status of I407F, The gene DDX50 has a mutation status of D543Y, The gene PALD1 has a mutation status of V509M, The gene POLR3A has a mutation status of I1117KfsTer23, The gene POLR3A has a mutation status of Y550C, The gene WAPL has a mutation status of G340R, The gene PAPSS2 has a mutation status of S68LfsTer19, The gene CC2D2B has a mutation status of K254N, The gene LCOR has a mutation status of N402Y, The gene SORCS1 has a mutation status of R696M, The gene DMBT1 has a mutation status of C537W, The gene FAM24A has a mutation status of I11V, The gene MUC5AC has a mutation status of C3226Ter, The gene OR52B6 has a mutation status of L295I, The gene AKIP1 has a mutation status of A113E, The gene PTPN5 has a mutation status of V234I, The gene LRP4 has a mutation status of A971S, The gene CELF1 has a mutation status of A256S, The gene MTCH2 has a mutation status of H119Y, The gene OR4C6 has a mutation status of C140G, The gene OR5L1 has a mutation status of S18L, The gene OR8K5 has a mutation status of R20L, The gene OR8U3 has a mutation status of D191Y, The gene ZDHHC5 has a mutation status of S673F, The gene OR9I1 has a mutation status of L312P, The gene OR5B2 has a mutation status of M134K, The gene OR4D10 has a mutation status of C240Ter, The gene OR4D11 has a mutation status of C189F, The gene MS4A8 has a mutation status of N56T, The gene MS4A18 has a mutation status of G72D, The gene AHNAK has a mutation status of D611N, The gene SLC22A25 has a mutation status of M21I, The gene SART1 has a mutation status of K414N, The gene TESMIN has a mutation status of K410N, The gene KRTAP5-10 has a mutation status of G119_G138del, The gene ARHGEF17 has a mutation status of R93S, The gene C2CD3 has a mutation status of L1437_Y1439del, The gene TPBGL has a mutation status of A143T, The gene RAB30 has a mutation status of S112R, The gene FAT3 has a mutation status of D2262Y, The gene JRKL has a mutation status of E85V, The gene BIRC3 has a mutation status of L174R, The gene ATM has a mutation status of G509A, The gene DIXDC1 has a mutation status of Q72L, The gene ZBTB16 has a mutation status of R566H, The gene NNMT has a mutation status of V83L, The gene CEP164 has a mutation status of Q1135K, The gene TBRG1 has a mutation status of L366F, The gene KIRREL3 has a mutation status of Q57K, The gene DYRK4 has a mutation status of L308F, The gene NDUFA9 has a mutation status of W108L, The gene VWF has a mutation status of G142S, The gene CHD4 has a mutation status of A935S, The gene C1S has a mutation status of P195L, The gene SLCO1A2 has a mutation status of G579E, The gene ABCC9 has a mutation status of Q802K, The gene CACNB3 has a mutation status of Q438PfsTer9, The gene PRPF40B has a mutation status of A118P, The gene KRT85 has a mutation status of R16S, The gene IGFBP6 has a mutation status of P106L, The gene NFE2 has a mutation status of E297_R300del, The gene KIF5A has a mutation status of Y936Ter, The gene TBC1D30 has a mutation status of Q149Ter, The gene ANKS1B has a mutation status of D837E, The gene ANKS1B has a mutation status of S35Y, The gene BLTP3B has a mutation status of S342A, The gene UTP20 has a mutation status of F732L, The gene MYBPC1 has a mutation status of I769T, The gene PARPBP has a mutation status of Q131K, The gene PAH has a mutation status of F402C, The gene MAPKAPK5 has a mutation status of I273M, The gene OAS2 has a mutation status of L311P, The gene TBX5 has a mutation status of P465L, The gene GCN1 has a mutation status of A1525V, The gene MORN3 has a mutation status of R166S, The gene KNTC1 has a mutation status of V1357L, The gene HIP1R has a mutation status of E308A, The gene DNAH10 has a mutation status of G4306E, The gene NOC4L has a mutation status of L493V, The gene XPO4 has a mutation status of D271N, The gene SPATA13 has a mutation status of A158E, The gene MTMR6 has a mutation status of G350D, The gene MTUS2 has a mutation status of Q1072K, The gene FRY has a mutation status of V341M, The gene ZC3H13 has a mutation status of H647Q, The gene CPB2 has a mutation status of S5I, The gene RUBCNL has a mutation status of L653I, The gene CKAP2 has a mutation status of T578S, The gene DACH1 has a mutation status of R650Q, The gene CCDC168 has a mutation status of A5113T, The gene LIG4 has a mutation status of Ter912SextTer2, The gene COL4A1 has a mutation status of Q523H, The gene COL4A2 has a mutation status of C483F, The gene UPF3A has a mutation status of E234Ter, The gene TEP1 has a mutation status of L2360F, The gene TTC6 has a mutation status of A69E, The gene TOGARAM1 has a mutation status of D35G, The gene FANCM has a mutation status of L1785V, The gene MDGA2 has a mutation status of C630S, The gene RTN1 has a mutation status of P538H, The gene PCNX1 has a mutation status of K520GfsTer2, The gene DNAL1 has a mutation status of V148L, The gene TTLL5 has a mutation status of Q1157K, The gene PPP2R5C has a mutation status of E179K, The gene CDC42BPB has a mutation status of S1683C, The gene INF2 has a mutation status of P1122H, The gene CDAN1 has a mutation status of R544L, The gene WDR76 has a mutation status of R573W, The gene TRPM7 has a mutation status of H1171Y, The gene VPS13C has a mutation status of F3261V, The gene TRIP4 has a mutation status of S140R, The gene HCN4 has a mutation status of W295S, The gene MAN2A2 has a mutation status of T79K, The gene HBQ1 has a mutation status of E31K, The gene WDR24 has a mutation status of A93T, The gene UNKL has a mutation status of D346V, The gene HS3ST6 has a mutation status of A36V, The gene E4F1 has a mutation status of E71K, The gene E4F1 has a mutation status of D130N, The gene RNPS1 has a mutation status of M189I, The gene ZSCAN32 has a mutation status of Q64Ter, The gene ABAT has a mutation status of Q264R, The gene ERCC4 has a mutation status of Q226H, The gene ABCC6 has a mutation status of A1128V, The gene SMG1 has a mutation status of A3251P, The gene AQP8 has a mutation status of A81S, The gene HS3ST4 has a mutation status of P115S, The gene PRR14 has a mutation status of A540T, The gene RNF40 has a mutation status of P543L, The gene LONP2 has a mutation status of D342E, The gene ZNF423 has a mutation status of T450K, The gene SALL1 has a mutation status of P317R, The gene TERB1 has a mutation status of Q352Ter, The gene SLC9A5 has a mutation status of Q445K, The gene PLA2G15 has a mutation status of M1?, The gene CDH1 has a mutation status of F39L, The gene CDH1 has a mutation status of T40K, The gene WWP2 has a mutation status of G344A, The gene ANKRD11 has a mutation status of Q1176K, The gene ANKRD11 has a mutation status of C1130Ter, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene ANKFY1 has a mutation status of S206R, The gene ZNF594 has a mutation status of E116V, The gene TP53 has a mutation status of R248Q, The gene USP43 has a mutation status of L344R, The gene MYH8 has a mutation status of K1531E, The gene MYH1 has a mutation status of L891S, The gene MPRIP has a mutation status of L1390F, The gene NOS2 has a mutation status of P706T, The gene AP2B1 has a mutation status of M448I, The gene MED1 has a mutation status of E881G, The gene RAPGEFL1 has a mutation status of L234P, The gene PSMC3IP has a mutation status of E200K, The gene UBTF has a mutation status of D740Y, The gene LRRC46 has a mutation status of C278S, The gene BCAS3 has a mutation status of P519S, The gene CEP95 has a mutation status of S116N, The gene KCNJ16 has a mutation status of E354Q, The gene CDC42EP4 has a mutation status of S292I, The gene MRPL38 has a mutation status of W6C, The gene CBX2 has a mutation status of S459N, The gene TYMS has a mutation status of S229I, The gene LAMA1 has a mutation status of L533FfsTer47, The gene PIEZO2 has a mutation status of G1753R, The gene MPPE1 has a mutation status of M166I, The gene ROCK1 has a mutation status of A1109G, The gene CELF4 has a mutation status of H213L, The gene CXXC1 has a mutation status of G565R, The gene TNFRSF11A has a mutation status of C169R, The gene PHLPP1 has a mutation status of S279W, The gene NETO1 has a mutation status of E144Q, The gene ZNF407 has a mutation status of H611Q, The gene ZNF516 has a mutation status of A554G, The gene PLPPR3 has a mutation status of E459K, The gene GRIN3B has a mutation status of P138L, The gene MEX3D has a mutation status of A55S, The gene KLF16 has a mutation status of S2L, The gene ZBTB7A has a mutation status of R483Ter, The gene PRAM1 has a mutation status of C658Y, The gene MYO1F has a mutation status of P995S, The gene S1PR2 has a mutation status of T320I, The gene TMEM205 has a mutation status of G8A, The gene ZNF440 has a mutation status of E169A, The gene ZNF700 has a mutation status of S459L, The gene WDR83 has a mutation status of R32Q, The gene CACNA1A has a mutation status of H2255N, The gene ILVBL has a mutation status of Q165Ter, The gene NOTCH3 has a mutation status of R1893Ter, The gene CYP4F22 has a mutation status of L197F, The gene INSL3 has a mutation status of Q92AfsTer62, The gene GDF1 has a mutation status of A255S, The gene ZNF729 has a mutation status of M1036I, The gene ZNF91 has a mutation status of T485S, The gene IGFLR1 has a mutation status of P163L, The gene ZNF527 has a mutation status of Q11H, The gene RYR1 has a mutation status of E1878V, The gene ZNF546 has a mutation status of T265I, The gene ATP1A3 has a mutation status of K81M, The gene ZNF404 has a mutation status of H433N, The gene ZNF224 has a mutation status of C206F, The gene PPP1R37 has a mutation status of S586A, The gene RSPH6A has a mutation status of M271R, The gene NTN5 has a mutation status of G284R, The gene PRR12 has a mutation status of P1003L, The gene SIGLEC7 has a mutation status of I372L, The gene HAS1 has a mutation status of H397Q, The gene ZNF665 has a mutation status of P289L, The gene ZNF761 has a mutation status of K613N, The gene OSCAR has a mutation status of A55E, The gene UBE2S has a mutation status of K100N, The gene SBK3 has a mutation status of D273Y, The gene ZNF805 has a mutation status of G497C, The gene MYT1L has a mutation status of A970V, The gene GEN1 has a mutation status of K721N, The gene APOB has a mutation status of C2933F, The gene APOB has a mutation status of Q436Ter, The gene KLHL29 has a mutation status of Q363TfsTer68, The gene ITSN2 has a mutation status of Q725L, The gene ALK has a mutation status of E1299K, The gene STON1 has a mutation status of P575L, The gene PEX13 has a mutation status of P235S, The gene DYSF has a mutation status of H746N, The gene TET3 has a mutation status of S1383PfsTer19, The gene LRRTM1 has a mutation status of N301K, The gene IGKV1-5 has a mutation status of T32N, The gene ZNF2 has a mutation status of E94Ter, The gene EN1 has a mutation status of R284L, The gene C1QL2 has a mutation status of A233V, The gene ARHGAP15 has a mutation status of K271I, The gene ZEB2 has a mutation status of D118G, The gene NEB has a mutation status of R3528C, The gene ACVR1 has a mutation status of G225D, The gene MARCHF7 has a mutation status of S64Y, The gene GPR155 has a mutation status of S96F, The gene HOXD11 has a mutation status of L174F, The gene TTC30B has a mutation status of G305R, The gene TTN has a mutation status of F27934L, The gene TTN has a mutation status of V16052L, The gene TTN has a mutation status of Q2087K, The gene FSIP2 has a mutation status of I2097NfsTer21, The gene FSIP2 has a mutation status of C2099PfsTer5, The gene C2CD6 has a mutation status of M1811KfsTer22, The gene C2CD6 has a mutation status of F1370C, The gene ANKZF1 has a mutation status of K435N, The gene DOCK10 has a mutation status of C238F, The gene TRIP12 has a mutation status of L536F, The gene UGT1A5 has a mutation status of L132M, The gene HDLBP has a mutation status of R534H, The gene DNAAF9 has a mutation status of R31Q, The gene PLCB1 has a mutation status of T869I, The gene XRN2 has a mutation status of I208T, The gene BPIFB1 has a mutation status of F388L, The gene KIAA1755 has a mutation status of E151D, The gene ZMYND8 has a mutation status of Q996RfsTer45, The gene PREX1 has a mutation status of E1135D, The gene KCNB1 has a mutation status of I544F, The gene APCDD1L has a mutation status of L221V, The gene PHACTR3 has a mutation status of E432K, The gene TAF4 has a mutation status of G177AfsTer22, The gene TAF4 has a mutation status of G175A, The gene LAMA5 has a mutation status of G275A, The gene DIDO1 has a mutation status of P1918L, The gene CHODL has a mutation status of T88S, The gene LTN1 has a mutation status of S532K, The gene LTN1 has a mutation status of S531K, The gene SPATC1L has a mutation status of P135S, The gene TBX1 has a mutation status of S41Ter, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene IGLV5-45 has a mutation status of A95T, The gene IGLV5-45 has a mutation status of I99L, The gene DDT has a mutation status of Q107K, The gene RFPL3 has a mutation status of L151C, The gene ZC3H7B has a mutation status of F585L, The gene SREBF2 has a mutation status of E658Ter, The gene PNPLA5 has a mutation status of C60WfsTer75, The gene SAMM50 has a mutation status of Q107H, The gene PARVB has a mutation status of R236L, The gene TAFA5 has a mutation status of G43V, The gene BRD1 has a mutation status of I60DfsTer6, The gene PANX2 has a mutation status of P414S, The gene ITPR1 has a mutation status of D1870H, The gene FANCD2OS has a mutation status of D122H, The gene C3orf20 has a mutation status of G449RfsTer6, The gene C3orf20 has a mutation status of G449C, The gene ZNF385D has a mutation status of S352N, The gene NKIRAS1 has a mutation status of D109E, The gene TOP2B has a mutation status of D231N, The gene TMPPE has a mutation status of P75Q, The gene TRANK1 has a mutation status of S2299F, The gene TRANK1 has a mutation status of P1317L, The gene MLH1 has a mutation status of L104WfsTer4, The gene CSRNP1 has a mutation status of Q260R, The gene CTNNB1 has a mutation status of T3I, The gene SCAP has a mutation status of I1020V, The gene ITIH4 has a mutation status of S248F, The gene CACNA2D3 has a mutation status of E724D, The gene CNTN3 has a mutation status of E177Ter, The gene EPHA3 has a mutation status of H76N, The gene CRYBG3 has a mutation status of L650QfsTer23, The gene OR5H1 has a mutation status of I158F, The gene DPPA2 has a mutation status of C96Y, The gene PODXL2 has a mutation status of P325H, The gene RHO has a mutation status of P327T, The gene PLXND1 has a mutation status of T1579M, The gene ACP3 has a mutation status of G45R, The gene TOPBP1 has a mutation status of S115RfsTer10, The gene ATR has a mutation status of L770K, The gene ATR has a mutation status of L769Q, The gene PLS1 has a mutation status of E262D, The gene P2RY12 has a mutation status of I257L, The gene IFT80 has a mutation status of M412T, The gene OTOL1 has a mutation status of R157P, The gene KLHL24 has a mutation status of R11I, The gene CCDC50 has a mutation status of Y144Ter, The gene OPA1 has a mutation status of M610T, The gene MUC4 has a mutation status of P2946T, The gene PDE6B has a mutation status of E747V, The gene HAUS3 has a mutation status of Q433K, The gene SEL1L3 has a mutation status of L519M, The gene RBPJ has a mutation status of S452A, The gene DTHD1 has a mutation status of E595G, The gene TXK has a mutation status of L53W, The gene GC has a mutation status of A318S, The gene AFM has a mutation status of K37N, The gene SHROOM3 has a mutation status of S1599Y, The gene C4orf54 has a mutation status of K1074N, The gene TET2 has a mutation status of P1655HfsTer6, The gene TET2 has a mutation status of P1655R, The gene PAPSS1 has a mutation status of M496L, The gene FAM241A has a mutation status of G11C, The gene NDST4 has a mutation status of N170D, The gene NDNF has a mutation status of L75F, The gene BLTP1 has a mutation status of T1521I, The gene ELF2 has a mutation status of M171K, The gene DCLK2 has a mutation status of A737G, The gene FGA has a mutation status of S364R, The gene SLC6A19 has a mutation status of L78M, The gene ADCY2 has a mutation status of E898Ter, The gene ADAMTS12 has a mutation status of A849S, The gene HMGCS1 has a mutation status of G122R, The gene PARP8 has a mutation status of H723R, The gene DHX29 has a mutation status of G691R, The gene RGS7BP has a mutation status of H103Q, The gene ANKRD31 has a mutation status of R606G, The gene VCAN has a mutation status of S1315G, The gene LYSMD3 has a mutation status of A221V, The gene C5orf24 has a mutation status of R92W, The gene TRPC7 has a mutation status of V685M, The gene PCDHA1 has a mutation status of A454E, The gene PCDHA5 has a mutation status of A48V, The gene FAT2 has a mutation status of R3649L, The gene GEMIN5 has a mutation status of S1267F, The gene GABRA1 has a mutation status of C166Y, The gene RPL26L1 has a mutation status of R11C, The gene GRM6 has a mutation status of S306Ter, The gene MGAT4B has a mutation status of R4L, The gene FLT4 has a mutation status of E1106Ter, The gene FARS2 has a mutation status of Y113C, The gene ATXN1 has a mutation status of E41D, The gene H4C1 has a mutation status of R20C, The gene PRRC2A has a mutation status of R853H, The gene CLIC1 has a mutation status of A98T, The gene PNPLA1 has a mutation status of I225V, The gene DNAH8 has a mutation status of R4629K, The gene C6orf132 has a mutation status of P989L, The gene IL17A has a mutation status of P31T, The gene FILIP1 has a mutation status of L681Q, The gene SYNCRIP has a mutation status of G155S, The gene AK9 has a mutation status of S1357G, The gene RSPH4A has a mutation status of E517D, The gene AHI1 has a mutation status of S232_E233delinsKK, The gene ADGB has a mutation status of V841I, The gene ZC3H12D has a mutation status of K526N, The gene RGS17 has a mutation status of M61L, The gene CNKSR3 has a mutation status of L344I, The gene LPA has a mutation status of W895L, The gene THBS2 has a mutation status of D813E, The gene CYP2W1 has a mutation status of R187Q, The gene ELFN1 has a mutation status of P276S, The gene ACTB has a mutation status of S368T, The gene THSD7A has a mutation status of E1014K, The gene HDAC9 has a mutation status of C680SfsTer2, The gene HOXA2 has a mutation status of N266K, The gene PDE1C has a mutation status of E595D, The gene IKZF1 has a mutation status of M311I, The gene EGFR has a mutation status of E746_A750del, The gene TYW1 has a mutation status of R406H, The gene BAZ1B has a mutation status of H1033Y, The gene SRRM3 has a mutation status of S508C, The gene ZP3 has a mutation status of F165L, The gene ZP3 has a mutation status of A227S, The gene PCLO has a mutation status of A2867D, The gene ZNF804B has a mutation status of C846F, The gene PEG10 has a mutation status of S392L, The gene PVRIG has a mutation status of S37Y, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of E725K, The gene MUC3A has a mutation status of S2495L, The gene MUC17 has a mutation status of S1639N, The gene VGF has a mutation status of G76AfsTer40, The gene ASZ1 has a mutation status of S271I, The gene CFTR has a mutation status of L1254Ter, The gene PLXNA4 has a mutation status of L883P, The gene WDR91 has a mutation status of R75H, The gene NUP205 has a mutation status of E700Q, The gene SLC37A3 has a mutation status of L415P, The gene HTR5A has a mutation status of I118V, The gene RBM33 has a mutation status of M695I, The gene CSMD1 has a mutation status of L1539V, The gene XKR6 has a mutation status of W333Ter, The gene SGCZ has a mutation status of L135F, The gene INTS10 has a mutation status of L348H, The gene LPL has a mutation status of L7F, The gene BNIP3L has a mutation status of L134F, The gene RAB11FIP1 has a mutation status of T1274KfsTer19, The gene OPRK1 has a mutation status of I133V, The gene CYP7B1 has a mutation status of D151H, The gene SULF1 has a mutation status of G529E, The gene RALYL has a mutation status of E195K, The gene BAALC has a mutation status of A35S, The gene PKHD1L1 has a mutation status of I4021S, The gene COL14A1 has a mutation status of V930I, The gene MTBP has a mutation status of T571K, The gene ZFAT has a mutation status of G740R, The gene FAM135B has a mutation status of G527W, The gene SPATC1 has a mutation status of E233K, The gene CPSF1 has a mutation status of A644D, The gene ARHGAP39 has a mutation status of G157RfsTer21, The gene PSIP1 has a mutation status of F43L, The gene CCDC171 has a mutation status of N157S, The gene CDKN2A has a mutation status of G67V, The gene CNTFR has a mutation status of S294C, The gene PAX5 has a mutation status of P320R, The gene NMRK1 has a mutation status of E42D, The gene SPATA31D1 has a mutation status of D183N, The gene IARS1 has a mutation status of P437L, The gene WNK2 has a mutation status of P972L, The gene ZNF510 has a mutation status of E59D, The gene ZNF462 has a mutation status of E1636K, The gene ABITRAM has a mutation status of A7S, The gene FRRS1L has a mutation status of G48E, The gene SHOC1 has a mutation status of E316K, The gene TLR4 has a mutation status of F768L, The gene OR1N2 has a mutation status of S275I, The gene TOR1A has a mutation status of F306V, The gene FIBCD1 has a mutation status of Q252H, The gene GTF3C5 has a mutation status of Q409K, The gene CCDC183 has a mutation status of L334R, The gene CACNA1B has a mutation status of A624V, The gene MT-ND1 has a mutation status of G29S, The gene MT-ND6 has a mutation status of E108D, The gene MT-CYB has a mutation status of A354T, The gene CTPS2 has a mutation status of R103C, The gene PPEF1 has a mutation status of V98E, The gene POLA1 has a mutation status of Q719H, The gene MAOB has a mutation status of P304_R307del, The gene FOXP3 has a mutation status of M64_P65delinsIT, The gene SLC16A2 has a mutation status of D523H, The gene POU3F4 has a mutation status of I94M, The gene BTK has a mutation status of G302R, The gene GPRASP3 has a mutation status of I289F, The gene ALG13 has a mutation status of S772N, The gene IL13RA2 has a mutation status of P241S, The gene TENM1 has a mutation status of E1861K, The gene CCDC160 has a mutation status of S27Y, The gene ZNF449 has a mutation status of G419E, The gene SLITRK4 has a mutation status of H297Y, The gene SLITRK2 has a mutation status of N799I, The gene CNGA2 has a mutation status of P433S, The gene MAGEA4 has a mutation status of G189S, The gene PNMA3 has a mutation status of A365E, The gene FAM50A has a mutation status of A58QfsTer11	LUAD
The gene PRXL2B has a mutation status of L103V, The gene FBXO44 has a mutation status of E59K, The gene LRRC8B has a mutation status of A236D, The gene MUC5AC has a mutation status of A5353K, The gene SSH3 has a mutation status of H651AfsTer2, The gene DYNC2H1 has a mutation status of D921E, The gene DYNC2H1 has a mutation status of Q2699K, The gene DSCAML1 has a mutation status of R409H, The gene KRAS has a mutation status of Q61R, The gene TMEM132D has a mutation status of A161T, The gene JAG2 has a mutation status of D701H, The gene TYRO3 has a mutation status of V233HfsTer11, The gene TGM7 has a mutation status of A306K, The gene DENND4A has a mutation status of K1882Q, The gene BNC1 has a mutation status of D271E, The gene USP31 has a mutation status of G442R, The gene VAT1L has a mutation status of K217M, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene TP53 has a mutation status of R273C, The gene MYH1 has a mutation status of S550F, The gene RAD51D has a mutation status of I105M, The gene ABCA8 has a mutation status of A479G, The gene SMARCA4 has a mutation status of T910M, The gene ZNF536 has a mutation status of A1095T, The gene ZNF586 has a mutation status of G212E, The gene CNNM3 has a mutation status of R246G, The gene CNNM3 has a mutation status of L249M, The gene RANBP2 has a mutation status of Q1054_P1055delinsHS, The gene MZT2A has a mutation status of L25G, The gene COL5A2 has a mutation status of P410S, The gene DNAH7 has a mutation status of P255R, The gene AOX1 has a mutation status of S502F, The gene ABCA12 has a mutation status of L855P, The gene NGEF has a mutation status of L102R, The gene KIF1A has a mutation status of P1185L, The gene KAT14 has a mutation status of N134RfsTer20, The gene SMC1B has a mutation status of Q601K, The gene PPP2R2C has a mutation status of R195C, The gene RAP1GDS1 has a mutation status of V451L, The gene PRDM5 has a mutation status of G258V, The gene FBXL7 has a mutation status of R198L, The gene SLCO4C1 has a mutation status of A373S, The gene SRPK1 has a mutation status of G50Ter, The gene SRPK1 has a mutation status of E47V, The gene GARS1 has a mutation status of S227F, The gene GNAI1 has a mutation status of Q106P, The gene LMTK2 has a mutation status of R1101P, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of S2495L, The gene ESYT2 has a mutation status of G198R, The gene BLK has a mutation status of R192PfsTer16, The gene PI15 has a mutation status of M67I, The gene VPS13B has a mutation status of T1673I, The gene MAFA has a mutation status of A329PfsTer95, The gene C5 has a mutation status of F1574L, The gene GAPVD1 has a mutation status of G1062S, The gene MT-ND4 has a mutation status of F50L, The gene MT-CYB has a mutation status of M316T, The gene RAB39B has a mutation status of E137K	PAAD
The gene PLCH2 has a mutation status of M55T, The gene COL9A2 has a mutation status of D52E, The gene SZT2 has a mutation status of D929G, The gene FOXD2 has a mutation status of L371P, The gene CPT2 has a mutation status of E81V, The gene USH2A has a mutation status of V2794D, The gene CDHR5 has a mutation status of V363M, The gene PCSK7 has a mutation status of H219Q, The gene OR8D2 has a mutation status of Y177Ter, The gene C2CD5 has a mutation status of Q193HfsTer5, The gene EIF4B has a mutation status of Y211C, The gene PPFIA2 has a mutation status of C1007W, The gene OASL has a mutation status of K66Q, The gene ATP11A has a mutation status of A1021T, The gene FANCM has a mutation status of P1477T, The gene TDRD9 has a mutation status of R691L, The gene CYP11A1 has a mutation status of M351I, The gene EDC3 has a mutation status of H297R, The gene GTF3C1 has a mutation status of A1404E, The gene SLC5A2 has a mutation status of T308I, The gene CNOT1 has a mutation status of A715T, The gene ANKRD11 has a mutation status of A2075V, The gene DNAH9 has a mutation status of Q2169H, The gene NCOR1 has a mutation status of Y2017C, The gene ZNF624 has a mutation status of N271D, The gene MYO15A has a mutation status of E2218K, The gene KCNJ12 has a mutation status of A382P, The gene ATAD5 has a mutation status of I134V, The gene CCDC103 has a mutation status of S190R, The gene PPP1R9B has a mutation status of G512S, The gene CDH2 has a mutation status of M287I, The gene MUC16 has a mutation status of M8698L, The gene RGL3 has a mutation status of E232KfsTer37, The gene KIR2DL3 has a mutation status of A304T, The gene TEX37 has a mutation status of M76K, The gene IL1RL1 has a mutation status of V89F, The gene THSD7B has a mutation status of S79C, The gene DOCK10 has a mutation status of Q1402H, The gene NANP has a mutation status of T119I, The gene UQCC1 has a mutation status of S285EfsTer48, The gene SEZ6L has a mutation status of T88A, The gene TAMM41 has a mutation status of Y320D, The gene CELSR3 has a mutation status of S120G, The gene RASSF1 has a mutation status of C82S, The gene LRTM1 has a mutation status of H261P, The gene SLITRK3 has a mutation status of Q796R, The gene ZNF639 has a mutation status of A72G, The gene LMLN has a mutation status of A380V, The gene FAM149A has a mutation status of W287L, The gene HTR1A has a mutation status of T13S, The gene LMNB1 has a mutation status of S288R, The gene GTF2H4 has a mutation status of E419K, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DQB2 has a mutation status of V37Y, The gene POM121L12 has a mutation status of A3S, The gene MUC3A has a mutation status of S2495L, The gene GPR37 has a mutation status of E74K, The gene SHH has a mutation status of A162T, The gene TRMT9B has a mutation status of R451G, The gene EBF2 has a mutation status of S28T, The gene PRSS3 has a mutation status of R122H, The gene MSL3 has a mutation status of D75G, The gene TCEAL6 has a mutation status of A50S, The gene HTATSF1 has a mutation status of R340H, The gene RBMX has a mutation status of G121R, The gene NSDHL has a mutation status of E289Ter	DLBC
The gene CDK11A has a mutation status of E107Ter, The gene HSPG2 has a mutation status of C879S, The gene TENT5B has a mutation status of H416R, The gene KHDC4 has a mutation status of N331H, The gene OR6N2 has a mutation status of P79L, The gene RYR2 has a mutation status of E535Q, The gene OR2T33 has a mutation status of S31A, The gene GLUD1 has a mutation status of H278Y, The gene TCTN3 has a mutation status of T333N, The gene CYP2R1 has a mutation status of K96Q, The gene PIK3C2A has a mutation status of C1524R, The gene CD5 has a mutation status of H461C, The gene MMP12 has a mutation status of E201K, The gene CWF19L2 has a mutation status of D491N, The gene C1R has a mutation status of G293E, The gene MUC19 has a mutation status of T3551A, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene MUC19 has a mutation status of N4824T, The gene KMT2D has a mutation status of E888_P889delinsA, The gene HVCN1 has a mutation status of M91T, The gene FRMD6 has a mutation status of T406I, The gene TTC7B has a mutation status of R271W, The gene LACTB has a mutation status of N277S, The gene DENND4A has a mutation status of T309A, The gene RASGRF1 has a mutation status of A985V, The gene MTHFS has a mutation status of V119I, The gene CIITA has a mutation status of E371D, The gene ZP2 has a mutation status of S401IfsTer7, The gene GABARAPL2 has a mutation status of S39F, The gene MYH1 has a mutation status of I1609N, The gene OMG has a mutation status of C11Y, The gene SERPINB3 has a mutation status of V134T, The gene SMARCA4 has a mutation status of N1164Y, The gene ZNF66 has a mutation status of T139A, The gene ZNF543 has a mutation status of R570K, The gene ZNF543 has a mutation status of E589Q, The gene ANKRD36C has a mutation status of A501E, The gene RAPH1 has a mutation status of E261Q, The gene CRLS1 has a mutation status of V6L, The gene CRLS1 has a mutation status of D147N, The gene ZFP64 has a mutation status of Q119L, The gene TAF4 has a mutation status of A767T, The gene OGFR has a mutation status of R565_P584del, The gene DIDO1 has a mutation status of E772K, The gene ADAMTS1 has a mutation status of F157S, The gene ERG has a mutation status of K89R, The gene PCNT has a mutation status of E3094Q, The gene DLEC1 has a mutation status of S412P, The gene ALDH1L1 has a mutation status of D346N, The gene EFCAB12 has a mutation status of S169F, The gene COL6A6 has a mutation status of G1455E, The gene KNG1 has a mutation status of P382L, The gene MUC4 has a mutation status of T3935P, The gene MUC4 has a mutation status of D3685N, The gene EDNRA has a mutation status of S289I, The gene FGA has a mutation status of W360GfsTer61, The gene FSTL4 has a mutation status of Ter843CextTer51, The gene HLA-DRB1 has a mutation status of S66N, The gene DSE has a mutation status of T866A, The gene DSE has a mutation status of K869I, The gene COL28A1 has a mutation status of I47T, The gene GSDME has a mutation status of S23L, The gene ANLN has a mutation status of V1107A, The gene EGFR has a mutation status of E746_A750del, The gene SBDS has a mutation status of I133V, The gene SEMA3A has a mutation status of V435I, The gene LAMB4 has a mutation status of I624V, The gene INTS10 has a mutation status of N200K, The gene SULF1 has a mutation status of M216I, The gene ERICH5 has a mutation status of D51H, The gene ERICH5 has a mutation status of D272H, The gene PKHD1L1 has a mutation status of C1543Ter, The gene SNTB1 has a mutation status of E336D, The gene KHDRBS3 has a mutation status of E320Q, The gene MROH1 has a mutation status of H375Q, The gene PRRC2B has a mutation status of A1276M, The gene MT-ND5 has a mutation status of T533M, The gene ARMCX5 has a mutation status of I552M	LUAD
The gene CSMD2 has a mutation status of F2196V, The gene ATP6V0B has a mutation status of L172F, The gene HOOK1 has a mutation status of W54GfsTer7, The gene UBQLN4 has a mutation status of S129Ter, The gene ARHGEF11 has a mutation status of E653KfsTer9, The gene LAMC1 has a mutation status of S131N, The gene IVNS1ABP has a mutation status of L236P, The gene ZNF281 has a mutation status of S69T, The gene PROX1 has a mutation status of M154V, The gene AIDA has a mutation status of F16L, The gene WDR64 has a mutation status of I214L, The gene DNAJC1 has a mutation status of I128V, The gene KIAA1217 has a mutation status of D592E, The gene KIAA1217 has a mutation status of S1786A, The gene KIAA1217 has a mutation status of F1790C, The gene ANKRD30A has a mutation status of R485V, The gene ZNF25 has a mutation status of E208G, The gene KNDC1 has a mutation status of L134I, The gene CCKBR has a mutation status of R411P, The gene PAX6 has a mutation status of Q60E, The gene FJX1 has a mutation status of A231T, The gene PRR5L has a mutation status of G359D, The gene NAA40 has a mutation status of R61Q, The gene TCIRG1 has a mutation status of A256S, The gene YAP1 has a mutation status of S340A, The gene DYNC2H1 has a mutation status of G2828A, The gene SIK3 has a mutation status of V925M, The gene TBRG1 has a mutation status of K24R, The gene TBRG1 has a mutation status of K27R, The gene ITFG2 has a mutation status of V240L, The gene GUCY2C has a mutation status of A48V, The gene DNM1L has a mutation status of S563N, The gene WNT1 has a mutation status of A20T, The gene RXYLT1 has a mutation status of F221L, The gene GCN1 has a mutation status of V1899M, The gene IPO5 has a mutation status of S851G, The gene RALGAPA1 has a mutation status of P1511L, The gene TTC6 has a mutation status of E252D, The gene TRIP11 has a mutation status of I1468R, The gene AHNAK2 has a mutation status of V2471L, The gene NIPA1 has a mutation status of E18G, The gene MEIS2 has a mutation status of M439V, The gene TYRO3 has a mutation status of S559_S560insTDIIAS, The gene MGA has a mutation status of E1427D, The gene CDAN1 has a mutation status of A230T, The gene TUBGCP4 has a mutation status of E338D, The gene NEO1 has a mutation status of G1282S, The gene HCN4 has a mutation status of V184A, The gene RPP25 has a mutation status of M50L, The gene KIF7 has a mutation status of P238H, The gene E4F1 has a mutation status of Q18G, The gene CCNF has a mutation status of G86Q, The gene NLRC3 has a mutation status of Q669R, The gene HAPSTR1 has a mutation status of S220P, The gene HAPSTR1 has a mutation status of S239T, The gene CIITA has a mutation status of R884S, The gene COQ7 has a mutation status of P194S, The gene ESRP2 has a mutation status of P19A, The gene CNTNAP4 has a mutation status of S1136R, The gene KIAA0513 has a mutation status of E333Q, The gene ZNF276 has a mutation status of V227I, The gene ZNF276 has a mutation status of V230A, The gene GAS8 has a mutation status of L265M, The gene TP53 has a mutation status of E326Ter, The gene SARM1 has a mutation status of G37C, The gene PIPOX has a mutation status of D291N, The gene NF1 has a mutation status of E1210Ter, The gene HIGD1B has a mutation status of R23K, The gene TNFSF9 has a mutation status of P249H, The gene KANK3 has a mutation status of G621S, The gene ZNF699 has a mutation status of A34G, The gene GIPC1 has a mutation status of G6W, The gene MAST3 has a mutation status of P372S, The gene SYMPK has a mutation status of D879H, The gene NTF4 has a mutation status of R45L, The gene SIGLEC9 has a mutation status of P302S, The gene C2orf16 has a mutation status of S2788Y, The gene GALNT14 has a mutation status of G496A, The gene CYP1B1 has a mutation status of R101S, The gene RAB11FIP5 has a mutation status of G136R, The gene NAT8B has a mutation status of Ter228RextTer?, The gene KANSL3 has a mutation status of G808S, The gene EN1 has a mutation status of A215G, The gene DARS1 has a mutation status of M18V, The gene DARS1 has a mutation status of S10G, The gene MBD5 has a mutation status of V374I, The gene MBD5 has a mutation status of M391V, The gene MBD5 has a mutation status of N1103I, The gene MBD5 has a mutation status of T1156P, The gene MBD5 has a mutation status of V1167M, The gene TBR1 has a mutation status of P597A, The gene IFIH1 has a mutation status of S282R, The gene IFIH1 has a mutation status of L270F, The gene TLK1 has a mutation status of Q18R, The gene RAPGEF4 has a mutation status of S487A, The gene RAPGEF4 has a mutation status of P725S, The gene SP3 has a mutation status of E402D, The gene SP3 has a mutation status of T325A, The gene SP3 has a mutation status of I320V, The gene ZNF385B has a mutation status of D204E, The gene MSTN has a mutation status of N197S, The gene SATB2 has a mutation status of I481V, The gene NDUFS1 has a mutation status of R113GfsTer4, The gene KLF7 has a mutation status of A115T, The gene FZD5 has a mutation status of Q19E, The gene CPS1 has a mutation status of L298I, The gene CPS1 has a mutation status of T308S, The gene IKZF2 has a mutation status of E98D, The gene ABCA12 has a mutation status of D505E, The gene SLC4A3 has a mutation status of P54T, The gene TRIP12 has a mutation status of A483P, The gene GIGYF2 has a mutation status of A1200V, The gene LRRN4 has a mutation status of A82G, The gene C20orf203 has a mutation status of G131W, The gene BPIFB6 has a mutation status of T96N, The gene RBM39 has a mutation status of Q424Ter, The gene PREX1 has a mutation status of G735W, The gene KCNB1 has a mutation status of V465I, The gene ATP5PF has a mutation status of R73M, The gene PAXBP1 has a mutation status of T384A, The gene SON has a mutation status of N2215S, The gene TTC3 has a mutation status of S310C, The gene DSCAM has a mutation status of L975I, The gene BACE2 has a mutation status of A326T, The gene NF2 has a mutation status of W74Ter, The gene RANGAP1 has a mutation status of G208W, The gene SELENOO has a mutation status of G644V, The gene LRRC3B has a mutation status of T257I, The gene CACNA2D2 has a mutation status of V957I, The gene USF3 has a mutation status of T686S, The gene ZNF148 has a mutation status of I134V, The gene PPP2R3A has a mutation status of R788K, The gene PARL has a mutation status of N161S, The gene RTP2 has a mutation status of A68P, The gene MUC4 has a mutation status of V2825A, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene CCNI has a mutation status of L169W, The gene CXXC4 has a mutation status of S37L, The gene FAT4 has a mutation status of K2892E, The gene SLC26A2 has a mutation status of H9R, The gene SLC36A2 has a mutation status of E286K, The gene JARID2 has a mutation status of T527P, The gene SLC44A4 has a mutation status of R281Q, The gene HLA-DQB1 has a mutation status of P84E, The gene KCNK5 has a mutation status of P372L, The gene PHF3 has a mutation status of A36T, The gene ZNF292 has a mutation status of T131I, The gene MFSD4B has a mutation status of L182Y, The gene HOXA13 has a mutation status of A296P, The gene SEPTIN7 has a mutation status of N325del, The gene LUC7L2 has a mutation status of S18Y, The gene DLGAP2 has a mutation status of N389T, The gene EYA1 has a mutation status of P93S, The gene JPH1 has a mutation status of G51V, The gene TAF1L has a mutation status of P1266L, The gene ZCCHC7 has a mutation status of D28Y, The gene ZCCHC7 has a mutation status of G147C, The gene PHF19 has a mutation status of H381Q, The gene GARNL3 has a mutation status of S486C, The gene EHMT1 has a mutation status of V212L, The gene CACNA1B has a mutation status of E2137D, The gene MXRA5 has a mutation status of S1147F, The gene ANOS1 has a mutation status of K161R, The gene SAGE1 has a mutation status of C82W, The gene ABCD1 has a mutation status of V86G	SARC
The gene BEND5 has a mutation status of Q191R, The gene MYSM1 has a mutation status of S432Ter, The gene GNG12 has a mutation status of I71V, The gene PHTF1 has a mutation status of V82I, The gene C1orf43 has a mutation status of V50del, The gene LY9 has a mutation status of T277R, The gene ASPM has a mutation status of L3178P, The gene TMEM183A has a mutation status of E89_I94delinsV, The gene C1orf115 has a mutation status of S14R, The gene MIA3 has a mutation status of I387V, The gene KIAA1217 has a mutation status of K44M, The gene GLUD1 has a mutation status of P121S, The gene MCMBP has a mutation status of N327K, The gene WDR11 has a mutation status of D332E, The gene MUC6 has a mutation status of A20T, The gene MRGPRE has a mutation status of H155P, The gene OR56B2P has a mutation status of G71C, The gene DNHD1 has a mutation status of E918D, The gene OR9G1 has a mutation status of M269L, The gene HTR3A has a mutation status of R432G, The gene IL10RA has a mutation status of W523R, The gene DHH has a mutation status of A391V, The gene PRDM4 has a mutation status of Q413H, The gene FBXW8 has a mutation status of A49D, The gene TMEM132B has a mutation status of S707R, The gene XPO4 has a mutation status of T154I, The gene CCNA1 has a mutation status of R59I, The gene LRFN5 has a mutation status of P586S, The gene OTX2 has a mutation status of I73V, The gene BCL11B has a mutation status of S2P, The gene EPB42 has a mutation status of E599G, The gene ARRDC4 has a mutation status of E48Ter, The gene BAIAP3 has a mutation status of T403A, The gene NETO2 has a mutation status of P162T, The gene CNGB1 has a mutation status of N758T, The gene PDF has a mutation status of V102G, The gene VPS9D1 has a mutation status of V399G, The gene POLR2A has a mutation status of N1251S, The gene GRIN2C has a mutation status of C1150F, The gene ENPP7 has a mutation status of T68P, The gene MOCOS has a mutation status of E659K, The gene TIMM29 has a mutation status of R47S, The gene BRD4 has a mutation status of R876G, The gene BRD4 has a mutation status of N875T, The gene ZNF493 has a mutation status of H763R, The gene SLC7A9 has a mutation status of R397I, The gene BLVRB has a mutation status of D80Y, The gene PXDN has a mutation status of D379E, The gene NCOA6 has a mutation status of K513Ter, The gene DOP1B has a mutation status of M2010T, The gene TRMT2A has a mutation status of L214I, The gene CSF2RB has a mutation status of R517G, The gene CADPS has a mutation status of E860K, The gene KALRN has a mutation status of Q390K, The gene HMX1 has a mutation status of S272P, The gene SMIM14 has a mutation status of I51N, The gene MMRN1 has a mutation status of A978P, The gene DDIT4L has a mutation status of C64Y, The gene DDX60 has a mutation status of F39V, The gene TRIO has a mutation status of N2724S, The gene MRPS27 has a mutation status of L240P, The gene ADGRV1 has a mutation status of L5037CfsTer11, The gene SLC22A4 has a mutation status of T394M, The gene RAD50 has a mutation status of M1?, The gene CAMLG has a mutation status of V16G, The gene BTN2A1 has a mutation status of G411E, The gene HLA-DRB5 has a mutation status of Q38W, The gene TCP11 has a mutation status of V271M, The gene ESR1 has a mutation status of F97S, The gene COL1A2 has a mutation status of M1257V, The gene MUC3A has a mutation status of T1234A, The gene NOBOX has a mutation status of G152A, The gene NOS3 has a mutation status of L832M, The gene XKR5 has a mutation status of I230V, The gene NRG1 has a mutation status of T430N, The gene C8orf34 has a mutation status of K183I, The gene VPS13B has a mutation status of N152K, The gene S1PR3 has a mutation status of T139A, The gene SLC44A1 has a mutation status of S8T, The gene CCDC187 has a mutation status of G975A, The gene ANAPC2 has a mutation status of D445G, The gene MT-ND4 has a mutation status of L238P, The gene MT-ND5 has a mutation status of T556I, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene MXRA5 has a mutation status of F141V, The gene PPP1R3F has a mutation status of G221V, The gene ABCD1 has a mutation status of P53H	DLBC
The gene MAP7D1 has a mutation status of S410T, The gene KCND3 has a mutation status of I111L, The gene VTCN1 has a mutation status of F174C, The gene BIRC2 has a mutation status of V324L, The gene DRD2 has a mutation status of R15K, The gene KMT2A has a mutation status of R130W, The gene GPR162 has a mutation status of W572R, The gene LRRIQ1 has a mutation status of I583V, The gene LRCH1 has a mutation status of H21Y, The gene RB1 has a mutation status of R698I, The gene SOX1 has a mutation status of Y2F, The gene ALDH6A1 has a mutation status of R107C, The gene SERPINA11 has a mutation status of G177V, The gene RPAP1 has a mutation status of L250V, The gene DAPK2 has a mutation status of R60GfsTer7, The gene ANKDD1A has a mutation status of N26S, The gene UBL7 has a mutation status of M212V, The gene RCCD1 has a mutation status of G38S, The gene ASB7 has a mutation status of G214R, The gene ZFP3 has a mutation status of S98I, The gene MRM1 has a mutation status of V149PfsTer43, The gene ASXL3 has a mutation status of K406E, The gene ZNF532 has a mutation status of V580M, The gene CALR3 has a mutation status of M13V, The gene NKPD1 has a mutation status of G374R, The gene TAF1B has a mutation status of S323N, The gene NOP58 has a mutation status of H144Y, The gene LAMA5 has a mutation status of L1510Q, The gene KRTAP15-1 has a mutation status of N39D, The gene BDH1 has a mutation status of K136T, The gene CLNK has a mutation status of R362C, The gene APBB2 has a mutation status of P214R, The gene SYNPO2 has a mutation status of C307R, The gene NR3C2 has a mutation status of F956L, The gene MSMO1 has a mutation status of H153R, The gene PDE8B has a mutation status of G92C, The gene FOXI1 has a mutation status of S236N, The gene HLA-DQB2 has a mutation status of V37Y, The gene FANCE has a mutation status of E56D, The gene UNC93A has a mutation status of F221L, The gene UNCX has a mutation status of S291R, The gene HECW1 has a mutation status of V1184T, The gene AKAP9 has a mutation status of K703Q, The gene MUC3A has a mutation status of T1234A, The gene ERI1 has a mutation status of L18M, The gene UBR5 has a mutation status of L1892_L1895delinsF, The gene TRAPPC9 has a mutation status of S925N, The gene HUWE1 has a mutation status of P2645H, The gene CLDN2 has a mutation status of P150Q, The gene GRIA3 has a mutation status of Q538H, The gene SOX3 has a mutation status of S288N, The gene MAGEA10 has a mutation status of A292S, The gene CAMTA1 has a mutation status of A812T, The gene KCND3 has a mutation status of I111L, The gene VTCN1 has a mutation status of F174C, The gene DENND1B has a mutation status of V426A, The gene NR5A2 has a mutation status of M428V, The gene IPO9 has a mutation status of V556M, The gene PIK3C2B has a mutation status of Q1596K, The gene CTNNA3 has a mutation status of V571A, The gene RAB11FIP2 has a mutation status of D368IfsTer19, The gene INPP5F has a mutation status of V640A, The gene NUCB2 has a mutation status of K400NfsTer15, The gene PSMC3 has a mutation status of Q14K, The gene MYRF has a mutation status of S51C, The gene AHNAK has a mutation status of D5198G, The gene FAT3 has a mutation status of G2128D, The gene ENDOD1 has a mutation status of L361M, The gene BIRC2 has a mutation status of V324L, The gene KMT2A has a mutation status of R130W, The gene GLB1L3 has a mutation status of R506K, The gene DCP1B has a mutation status of I16T, The gene GPR162 has a mutation status of W572R, The gene MUC19 has a mutation status of N6618_I6619delinsSV, The gene DGKA has a mutation status of R726AfsTer9, The gene LRRIQ1 has a mutation status of I583V, The gene SETD1B has a mutation status of T622N, The gene PIWIL1 has a mutation status of A681T, The gene SACS has a mutation status of I2747FfsTer6, The gene RB1 has a mutation status of R698I, The gene RCBTB2 has a mutation status of L369I, The gene COL4A2 has a mutation status of G1143C, The gene OR4M1 has a mutation status of S156Y, The gene MDGA2 has a mutation status of G104C, The gene SOS2 has a mutation status of R20L, The gene ALDH6A1 has a mutation status of R107C, The gene RIN3 has a mutation status of R949C, The gene IGHD has a mutation status of E155DfsTer41, The gene RPAP1 has a mutation status of L250V, The gene SLC12A1 has a mutation status of M195V, The gene GALK2 has a mutation status of K426N, The gene DAPK2 has a mutation status of R60GfsTer7, The gene ANKDD1A has a mutation status of N26S, The gene UBL7 has a mutation status of M212V, The gene ASB7 has a mutation status of G214R, The gene CACNA1H has a mutation status of L1540I, The gene NTAN1 has a mutation status of G84C, The gene ZNF19 has a mutation status of R265K, The gene KCNG4 has a mutation status of A311T, The gene WDR81 has a mutation status of L721I, The gene KDM6B has a mutation status of T896PfsTer19, The gene RAPGEFL1 has a mutation status of P119T, The gene CLTC has a mutation status of A352D, The gene MED13 has a mutation status of R1319Ter, The gene CD300H has a mutation status of G27C, The gene ASXL3 has a mutation status of K406E, The gene LOXHD1 has a mutation status of Y2164Ter, The gene ZNF532 has a mutation status of V580M, The gene SLC44A2 has a mutation status of R590I, The gene ZNF69 has a mutation status of T269S, The gene CALR3 has a mutation status of M13V, The gene ZNF230 has a mutation status of V122A, The gene TAF1B has a mutation status of S323N, The gene XDH has a mutation status of T934A, The gene GAD1 has a mutation status of T576A, The gene TTN has a mutation status of T5988A, The gene NOP58 has a mutation status of H144Y, The gene INO80D has a mutation status of E619G, The gene MCM8 has a mutation status of M383T, The gene GZF1 has a mutation status of Y505H, The gene BPIFB4 has a mutation status of K417N, The gene LAMA5 has a mutation status of L1510Q, The gene KRTAP15-1 has a mutation status of N39D, The gene SLC19A1 has a mutation status of A78V, The gene NR2C2 has a mutation status of F563LfsTer10, The gene NEK10 has a mutation status of T58R, The gene SCN11A has a mutation status of P77S, The gene KLHDC8B has a mutation status of M17CfsTer59, The gene GMPPB has a mutation status of G9S, The gene GRAMD1C has a mutation status of N208K, The gene ATR has a mutation status of T415A, The gene ABCF3 has a mutation status of M534I, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene MUC4 has a mutation status of P1378H, The gene BDH1 has a mutation status of K136T, The gene CLNK has a mutation status of R362C, The gene APBB2 has a mutation status of P214R, The gene FAM47E has a mutation status of L133M, The gene ABCG2 has a mutation status of N418MfsTer16, The gene SYNPO2 has a mutation status of C307R, The gene MSMO1 has a mutation status of H153R, The gene RAI14 has a mutation status of I145T, The gene PLPP1 has a mutation status of V133I, The gene GCNT4 has a mutation status of H294IfsTer14, The gene TSLP has a mutation status of H74Y, The gene FAM170A has a mutation status of E290D, The gene PCDHA2 has a mutation status of A703T, The gene HLA-A has a mutation status of I121R, The gene HCG22 has a mutation status of G126V, The gene HLA-DRB1 has a mutation status of S66N, The gene HLA-DQB1 has a mutation status of P84E, The gene SPDEF has a mutation status of D21RfsTer44, The gene EYS has a mutation status of G1108R, The gene RNF217 has a mutation status of E3D, The gene UNC93A has a mutation status of F221L, The gene BRAT1 has a mutation status of G189VfsTer30, The gene STARD3NL has a mutation status of G206D, The gene HECW1 has a mutation status of V1184T, The gene ELN has a mutation status of G340C, The gene AKAP9 has a mutation status of K703Q, The gene MUC3A has a mutation status of T1234A, The gene MKRN1 has a mutation status of I342V, The gene ZNF425 has a mutation status of C391R, The gene UBR5 has a mutation status of L1892_L1895delinsF, The gene ANKRD18A has a mutation status of R547H, The gene TMOD1 has a mutation status of V339L, The gene CRB2 has a mutation status of D978G, The gene SHROOM2 has a mutation status of A1085T, The gene TMSB4X has a mutation status of A8V, The gene PHF8 has a mutation status of D824Y, The gene P2RY4 has a mutation status of Y197N, The gene CLDN2 has a mutation status of P150Q, The gene KIAA1210 has a mutation status of M82T, The gene GRIA3 has a mutation status of Q538H, The gene SOX3 has a mutation status of S288N, The gene MAGEA10 has a mutation status of A292S, The gene PLXNB3 has a mutation status of A1263T, The gene PLXNB3 has a mutation status of W1750R	SARC
The gene MTOR has a mutation status of L1129P, The gene DISP3 has a mutation status of E454AfsTer7, The gene KLF18 has a mutation status of P59L, The gene CCDC18 has a mutation status of L1438F, The gene POGZ has a mutation status of S329F, The gene C1orf68 has a mutation status of P165L, The gene ARHGEF11 has a mutation status of E721V, The gene APCS has a mutation status of P196A, The gene TDRD5 has a mutation status of S96R, The gene NAV1 has a mutation status of A285E, The gene RNPEP has a mutation status of K190T, The gene MAPKAPK2 has a mutation status of Q113P, The gene NVL has a mutation status of K226N, The gene H3-4 has a mutation status of E74K, The gene ZNF496 has a mutation status of P292T, The gene OR2T33 has a mutation status of L205P, The gene CFAP70 has a mutation status of L1056V, The gene BTRC has a mutation status of M160L, The gene NEURL1 has a mutation status of G438R, The gene CPXM2 has a mutation status of R406H, The gene TTC17 has a mutation status of I603F, The gene TRIM51 has a mutation status of L41I, The gene RAB3IL1 has a mutation status of A183S, The gene CCS has a mutation status of N142K, The gene TSKU has a mutation status of P326H, The gene CCND2 has a mutation status of P281A, The gene SCNN1A has a mutation status of R181W, The gene RPAP3 has a mutation status of E657K, The gene NCKAP5L has a mutation status of A858D, The gene ARHGEF25 has a mutation status of T360N, The gene UTP20 has a mutation status of I1873T, The gene ABTB3 has a mutation status of P278T, The gene RBM19 has a mutation status of E264Ter, The gene OGFOD2 has a mutation status of G50R, The gene SUCLA2 has a mutation status of R20G, The gene ATP7B has a mutation status of I582V, The gene UNC79 has a mutation status of W2242Ter, The gene JAG2 has a mutation status of D888Y, The gene EMC4 has a mutation status of A18D, The gene NEO1 has a mutation status of S161C, The gene ANKS4B has a mutation status of I363V, The gene ARMC5 has a mutation status of C273S, The gene GEMIN4 has a mutation status of K117R, The gene ZZEF1 has a mutation status of A2953P, The gene TP53 has a mutation status of R213Q, The gene MYH3 has a mutation status of G361R, The gene BAHCC1 has a mutation status of H279P, The gene DSG2 has a mutation status of P97R, The gene MIDN has a mutation status of S108C, The gene PTPRS has a mutation status of G1454C, The gene GPR108 has a mutation status of F403L, The gene DNMT1 has a mutation status of K351R, The gene RINL has a mutation status of G396V, The gene FCGBP has a mutation status of A1165GfsTer13, The gene FCGBP has a mutation status of E1160GfsTer144, The gene ZNF224 has a mutation status of K314T, The gene LILRA4 has a mutation status of S302P, The gene ZNF837 has a mutation status of R457Q, The gene SLC27A5 has a mutation status of A324T, The gene CAPN14 has a mutation status of I565T, The gene XDH has a mutation status of G739C, The gene BCL11A has a mutation status of D798N, The gene FBXO41 has a mutation status of Q717SfsTer15, The gene MBD5 has a mutation status of P1351Q, The gene GPR55 has a mutation status of F199C, The gene SLC4A11 has a mutation status of I658F, The gene LAMA5 has a mutation status of L2185P, The gene IGSF5 has a mutation status of T405N, The gene GP1BB has a mutation status of A139S, The gene GRK3 has a mutation status of I150V, The gene OSBP2 has a mutation status of L494P, The gene GRM7 has a mutation status of G332R, The gene CCK has a mutation status of I92V, The gene SACM1L has a mutation status of A52T, The gene DNAH1 has a mutation status of S682FfsTer3, The gene PRR20G has a mutation status of S208F, The gene SENP2 has a mutation status of T265A, The gene ST6GAL1 has a mutation status of K88Q, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene RASGEF1B has a mutation status of E128Q, The gene PRDM5 has a mutation status of K610E, The gene ARHGEF28 has a mutation status of P742Q, The gene FAT2 has a mutation status of G4306V, The gene PRR7 has a mutation status of H89Q, The gene RASGEF1C has a mutation status of E433D, The gene DSP has a mutation status of K906Ter, The gene H2AC16 has a mutation status of R30P, The gene PPP1R10 has a mutation status of E339G, The gene KCNK16 has a mutation status of D275N, The gene NMBR has a mutation status of D297H, The gene FZD1 has a mutation status of E33G, The gene MUC17 has a mutation status of T2355M, The gene FASTK has a mutation status of G51S, The gene ADGRA2 has a mutation status of K1184R, The gene ZBTB10 has a mutation status of K304I, The gene CHMP4C has a mutation status of S13C, The gene SPAG1 has a mutation status of I95LfsTer5, The gene LRATD2 has a mutation status of P21S, The gene DNAAF11 has a mutation status of M413I, The gene SLA has a mutation status of D200S, The gene CYP11B1 has a mutation status of P491L, The gene RHPN1 has a mutation status of E618D, The gene GNE has a mutation status of T3A, The gene STRBP has a mutation status of Y647C, The gene SEC16A has a mutation status of P2065S, The gene TUBB4B has a mutation status of F20C, The gene TBL1X has a mutation status of N266T, The gene SHROOM4 has a mutation status of R409C, The gene CTAG2 has a mutation status of A60T, The gene KDM5D has a mutation status of T1084R	GBMLGG
The gene ARHGEF19 has a mutation status of A686V, The gene OTUD3 has a mutation status of Q61P, The gene NIPAL3 has a mutation status of P175T, The gene TENT5B has a mutation status of H416R, The gene RIMKLA has a mutation status of H53Y, The gene LINGO4 has a mutation status of G251R, The gene ADCY10 has a mutation status of E756K, The gene TDRD5 has a mutation status of I789T, The gene ZNF281 has a mutation status of K594R, The gene KCNK1 has a mutation status of S112I, The gene TAF6L has a mutation status of S512P, The gene SRSF8 has a mutation status of D19E, The gene CLEC1A has a mutation status of L59F, The gene CPNE8 has a mutation status of R542L, The gene MYO1H has a mutation status of A363E, The gene FRY has a mutation status of R1999L, The gene PCDH8 has a mutation status of Q101K, The gene PCK2 has a mutation status of L77M, The gene TOGARAM1 has a mutation status of F786LfsTer113, The gene AHNAK2 has a mutation status of V2471L, The gene CAPN3 has a mutation status of Y89H, The gene CSPG4 has a mutation status of A1331P, The gene WDR93 has a mutation status of L358F, The gene CLUH has a mutation status of S1197I, The gene TP53 has a mutation status of R273C, The gene MYH8 has a mutation status of E1352D, The gene CASC3 has a mutation status of Q672K, The gene MTMR4 has a mutation status of K391R, The gene CACNG4 has a mutation status of R240Q, The gene FBF1 has a mutation status of A919G, The gene FAM210A has a mutation status of R201W, The gene ZBTB7C has a mutation status of P321T, The gene GRIK5 has a mutation status of G897V, The gene PXDN has a mutation status of E1041K, The gene PCARE has a mutation status of Q1020R, The gene FLACC1 has a mutation status of P5H, The gene TMEM198 has a mutation status of S316N, The gene SNRPB2 has a mutation status of A65S, The gene CLIC6 has a mutation status of D616E, The gene PDE12 has a mutation status of S98_P100du, The gene NR2F1 has a mutation status of A195T, The gene SH3TC2 has a mutation status of A468F, The gene SPDL1 has a mutation status of R453S, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB2 has a mutation status of V37Y, The gene CAPN11 has a mutation status of K640E, The gene OOEP has a mutation status of A56V, The gene TNFAIP3 has a mutation status of D169N, The gene LRP11 has a mutation status of F117L, The gene GPER1 has a mutation status of E218P, The gene EGFR has a mutation status of M600V, The gene GPR37 has a mutation status of P253S, The gene STRIP2 has a mutation status of F250L, The gene KEL has a mutation status of A580D, The gene OR10AC1 has a mutation status of P132Q, The gene CNTNAP2 has a mutation status of E282Ter, The gene LOXL2 has a mutation status of E210D, The gene PTK2B has a mutation status of C562G, The gene GPSM1 has a mutation status of E392Ter, The gene TPRN has a mutation status of E607Q, The gene STARD8 has a mutation status of G383D	SARC
The gene ARID1A has a mutation status of L2239P, The gene LRRC7 has a mutation status of R605Ter, The gene RPF1 has a mutation status of F267SfsTer3, The gene SLAMF7 has a mutation status of D266S, The gene RHEX has a mutation status of N145I, The gene SRGAP2 has a mutation status of R840C, The gene OBSCN has a mutation status of R3219Ter, The gene JCAD has a mutation status of R799W, The gene KIFBP has a mutation status of E240V, The gene STAMBPL1 has a mutation status of L110P, The gene PPP1R32 has a mutation status of Q80Ter, The gene FEN1 has a mutation status of I44L, The gene TSGA10IP has a mutation status of Q530P, The gene FAT3 has a mutation status of N3992Y, The gene TECTA has a mutation status of K1325N, The gene TAS2R43 has a mutation status of N76C, The gene KRAS has a mutation status of G12D, The gene ITGA7 has a mutation status of A785G, The gene BAZ1A has a mutation status of I640V, The gene CENPT has a mutation status of F467C, The gene PKD1L3 has a mutation status of N426S, The gene POLR2A has a mutation status of P1732L, The gene TP53 has a mutation status of R248Q, The gene CD300LG has a mutation status of M218I, The gene SAMD14 has a mutation status of K392N, The gene SMAD4 has a mutation status of R135Ter, The gene PLIN4 has a mutation status of A807S, The gene PNPLA6 has a mutation status of Q746Ter, The gene MUC16 has a mutation status of M8698V, The gene CC2D1A has a mutation status of E90D, The gene ZNF493 has a mutation status of K564E, The gene CATSPERG has a mutation status of Y835F, The gene LILRA2 has a mutation status of W175S, The gene KIF3C has a mutation status of E470K, The gene ZFP36L2 has a mutation status of T100HfsTer3, The gene MAP4K4 has a mutation status of P967S, The gene IL1RL1 has a mutation status of P114T, The gene COL4A4 has a mutation status of E60Q, The gene COL4A3 has a mutation status of L1490F, The gene HDLBP has a mutation status of K1152N, The gene ZNFX1 has a mutation status of G80E, The gene HSPA13 has a mutation status of D258N, The gene C22orf31 has a mutation status of L160V, The gene PES1 has a mutation status of D400N, The gene FBXO7 has a mutation status of E405Ter, The gene SYN3 has a mutation status of S473F, The gene CACNA1I has a mutation status of S1996F, The gene PLXNB2 has a mutation status of T79K, The gene VILL has a mutation status of S348F, The gene MELTF has a mutation status of C369R, The gene HAUS3 has a mutation status of D236N, The gene SLC10A4 has a mutation status of W89C, The gene ABRAXAS1 has a mutation status of S376G, The gene PTPN13 has a mutation status of L9M, The gene UNC5C has a mutation status of P604S, The gene SUB1 has a mutation status of Q30LfsTer7, The gene VCAN has a mutation status of A2208F, The gene WDR36 has a mutation status of H156P, The gene DDX46 has a mutation status of V597M, The gene GEMIN5 has a mutation status of D931V, The gene H4C3 has a mutation status of E53K, The gene H4C5 has a mutation status of A16V, The gene MUC3A has a mutation status of S2495L, The gene PLOD3 has a mutation status of G120V, The gene PTN has a mutation status of R71Q, The gene KEL has a mutation status of M440R, The gene EPHX2 has a mutation status of F182Y, The gene ZFHX4 has a mutation status of D2340H, The gene CDKN2A has a mutation status of Y44Ter, The gene DMRTA1 has a mutation status of R93Q, The gene DCTN3 has a mutation status of L68V, The gene WNK3 has a mutation status of S344L, The gene FAM133A has a mutation status of T53NfsTer8, The gene OR13H1 has a mutation status of D295E, The gene AFF2 has a mutation status of V1196F, The gene GAB3 has a mutation status of C410F	PAAD
The gene ATAD3B has a mutation status of L350P, The gene ARID1A has a mutation status of Q1212Ter, The gene COL24A1 has a mutation status of E718K, The gene ABCA4 has a mutation status of D596N, The gene SARS1 has a mutation status of A186V, The gene PIGC has a mutation status of G159S, The gene OR2L2 has a mutation status of L221I, The gene OTUD1 has a mutation status of S326C, The gene OPN4 has a mutation status of A274V, The gene SORCS3 has a mutation status of P122A, The gene MICAL2 has a mutation status of Q450Ter, The gene TMEM109 has a mutation status of Q105H, The gene GRM5 has a mutation status of K867N, The gene CD3E has a mutation status of D23H, The gene MUC19 has a mutation status of D5371Y, The gene GALNT6 has a mutation status of M376I, The gene KRT77 has a mutation status of E432TfsTer19, The gene TBC1D30 has a mutation status of R46W, The gene TMEM132C has a mutation status of K1052Ter, The gene ALG5 has a mutation status of L11V, The gene ZFYVE1 has a mutation status of H268D, The gene BBOF1 has a mutation status of T122I, The gene GOLGA6L2 has a mutation status of D196N, The gene WDR76 has a mutation status of D149N, The gene USP8 has a mutation status of N403S, The gene VPS13C has a mutation status of R771Ter, The gene ZNF500 has a mutation status of Q51E, The gene PKD1L2 has a mutation status of T1446K, The gene NCBP3 has a mutation status of D208H, The gene MAP2K4 has a mutation status of S184L, The gene DHX8 has a mutation status of S374PfsTer8, The gene TSEN54 has a mutation status of S492C, The gene DNAH17 has a mutation status of E1961Q, The gene FHOD3 has a mutation status of F1029P, The gene MC4R has a mutation status of I173M, The gene SH2D3A has a mutation status of K208Q, The gene RAB3D has a mutation status of T78A, The gene GET3 has a mutation status of E120K, The gene IER2 has a mutation status of S67Y, The gene RASGRP4 has a mutation status of R252L, The gene LILRB3 has a mutation status of W205Q, The gene NLRP8 has a mutation status of K885Q, The gene ZNF671 has a mutation status of Q490E, The gene LRPPRC has a mutation status of L238F, The gene THSD7B has a mutation status of L1567V, The gene BAZ2B has a mutation status of S1432F, The gene KCNJ4 has a mutation status of R427L, The gene PRR5 has a mutation status of E117Q, The gene SMC1B has a mutation status of Q880H, The gene TBC1D5 has a mutation status of I213V, The gene UBE2E2 has a mutation status of H129D, The gene XCR1 has a mutation status of V187F, The gene PTPRG has a mutation status of C1362F, The gene CPOX has a mutation status of S112L, The gene U2SURP has a mutation status of D802H, The gene MUC4 has a mutation status of T3620S, The gene MFSD10 has a mutation status of A135D, The gene EVC2 has a mutation status of R796K, The gene ARAP2 has a mutation status of D641E, The gene MMRN1 has a mutation status of D726N, The gene ADH6 has a mutation status of A72S, The gene GPM6A has a mutation status of G24D, The gene AGA has a mutation status of D80H, The gene IRF2 has a mutation status of E295D, The gene LVRN has a mutation status of E203V, The gene PCDHGB2 has a mutation status of E310Q, The gene PCDHGB2 has a mutation status of E463Q, The gene NRN1 has a mutation status of V77I, The gene HLA-DRB5 has a mutation status of Y42H, The gene CYB5R4 has a mutation status of L125Q, The gene CITED2 has a mutation status of A203T, The gene PHACTR2 has a mutation status of P211S, The gene GHRHR has a mutation status of L332H, The gene ERVW-1 has a mutation status of L333Ter, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of N2136_E2152del, The gene ARHGEF10 has a mutation status of E423K, The gene MSR1 has a mutation status of T264A, The gene HNF4G has a mutation status of S429L, The gene LRP12 has a mutation status of A23S, The gene DENND4C has a mutation status of D488E, The gene PRSS3 has a mutation status of D102I, The gene ZNF169 has a mutation status of E27Q, The gene TRMO has a mutation status of S367L, The gene TRIM14 has a mutation status of V66G, The gene GALNT12 has a mutation status of E273D, The gene FKBP15 has a mutation status of G372S, The gene HMCN2 has a mutation status of A507T, The gene USP11 has a mutation status of P698L, The gene CLCN5 has a mutation status of V262F, The gene HUWE1 has a mutation status of M495I, The gene GNL3L has a mutation status of E104D, The gene ARMCX4 has a mutation status of G1814_A1815insTEAGAG, The gene GPRASP1 has a mutation status of I1174T, The gene ELF4 has a mutation status of E86Q	BRCA
The gene ARHGEF16 has a mutation status of G143D, The gene EPHA10 has a mutation status of A403G, The gene NRDC has a mutation status of R540I, The gene HOOK1 has a mutation status of R272H, The gene EFCAB7 has a mutation status of A41T, The gene EVI5 has a mutation status of D739G, The gene CELSR2 has a mutation status of R2015K, The gene AHCYL1 has a mutation status of C392Y, The gene AHCYL1 has a mutation status of I393L, The gene RO60 has a mutation status of E3DfsTer3, The gene SPATA17 has a mutation status of E119Ter, The gene RAB3GAP2 has a mutation status of Q1214K, The gene LYST has a mutation status of A1284T, The gene OR2T8 has a mutation status of F236LfsTer23, The gene TAF3 has a mutation status of M154SfsTer39, The gene CELF2 has a mutation status of M32I, The gene PTCHD3 has a mutation status of E477D, The gene CCDC186 has a mutation status of R457I, The gene DNHD1 has a mutation status of T4106A, The gene TM7SF2 has a mutation status of L106P, The gene DYNC2H1 has a mutation status of L2157Q, The gene TRHDE has a mutation status of I863T, The gene LIN7A has a mutation status of G117D, The gene TCTN2 has a mutation status of D331N, The gene FLT3 has a mutation status of D600_L601insHVDFREYEYD, The gene IRS2 has a mutation status of P1273_P1274del, The gene TTC6 has a mutation status of E252D, The gene DCAF4 has a mutation status of I394L, The gene ATG2B has a mutation status of C1847R, The gene CEP170B has a mutation status of D322Ter, The gene IGHV4-61 has a mutation status of D93E, The gene RYR3 has a mutation status of R835S, The gene GALK2 has a mutation status of Q358Ter, The gene SLX4 has a mutation status of L612P, The gene KLHL36 has a mutation status of R291G, The gene PCGF2 has a mutation status of T311del, The gene PCGF2 has a mutation status of P300_G308del, The gene SMARCE1 has a mutation status of S172N, The gene CABLES1 has a mutation status of P49L, The gene ZNF521 has a mutation status of E748Q, The gene MBD1 has a mutation status of D531H, The gene MC4R has a mutation status of S136P, The gene GRIN3B has a mutation status of P448R, The gene TIMM44 has a mutation status of E431Ter, The gene GTPBP3 has a mutation status of P68S, The gene ZNF257 has a mutation status of C126H, The gene CKM has a mutation status of R314C, The gene ZNF649 has a mutation status of I502V, The gene RALB has a mutation status of A116P, The gene MYO3B has a mutation status of G377V, The gene NRSN2 has a mutation status of S4T, The gene ARFRP1 has a mutation status of D146E, The gene FBLN2 has a mutation status of R527T, The gene NEK4 has a mutation status of G284V, The gene DHX36 has a mutation status of Q430_E431delinsHTer, The gene MUC4 has a mutation status of D3685N, The gene ARAP2 has a mutation status of K922NfsTer10, The gene COX18 has a mutation status of A15V, The gene C4orf54 has a mutation status of H366_Y367delinsQD, The gene ENPEP has a mutation status of A80G, The gene DCHS2 has a mutation status of V1209Ter, The gene GLRB has a mutation status of A348V, The gene PDZD2 has a mutation status of S2112_R2114del, The gene C7 has a mutation status of T158A, The gene ISOC1 has a mutation status of A7L, The gene HLA-DRB1 has a mutation status of T106N, The gene KHDC1 has a mutation status of H21L, The gene GPRC6A has a mutation status of A425S, The gene CPVL has a mutation status of K469Q, The gene PDE1C has a mutation status of S592A, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of M384T, The gene LRWD1 has a mutation status of R416Q, The gene PTPRZ1 has a mutation status of A195E, The gene POT1 has a mutation status of K39E, The gene ADAM7 has a mutation status of E518D, The gene NBN has a mutation status of K690Q, The gene LAPTM4B has a mutation status of M88K, The gene PPP1R16A has a mutation status of D385N, The gene OR1N2 has a mutation status of Y269S, The gene EHMT1 has a mutation status of L1059V, The gene PHKA2 has a mutation status of H132PfsTer29, The gene PPP1R3F has a mutation status of R127C	LAML
The gene SPEN has a mutation status of A3248P, The gene CYP4Z1 has a mutation status of W356Ter, The gene MIGA1 has a mutation status of V49A, The gene IGFN1 has a mutation status of A2230E, The gene CCDC7 has a mutation status of V347M, The gene RBP3 has a mutation status of I183T, The gene WDFY4 has a mutation status of V2992L, The gene ADD3 has a mutation status of E702del, The gene PSTK has a mutation status of R16Q, The gene OR52P1 has a mutation status of S124L, The gene DPF2 has a mutation status of C345F, The gene ART4 has a mutation status of V49I, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene NAA25 has a mutation status of S316R, The gene SETD1B has a mutation status of P203L, The gene TMEM132C has a mutation status of D650H, The gene SYNE2 has a mutation status of K3229N, The gene AKAP5 has a mutation status of I130M, The gene IGHM has a mutation status of K315Q, The gene UNKL has a mutation status of N85K, The gene ASPHD1 has a mutation status of R186H, The gene BHLHA9 has a mutation status of A183V, The gene ATP6V0A1 has a mutation status of M758T, The gene MYO5B has a mutation status of P1615Q, The gene POLR2E has a mutation status of P178S, The gene TICAM1 has a mutation status of L549R, The gene MEGF8 has a mutation status of G407D, The gene LIPE has a mutation status of A359V, The gene PSG3 has a mutation status of P3T, The gene PSG1 has a mutation status of D116G, The gene ELSPBP1 has a mutation status of N213S, The gene KASH5 has a mutation status of E317K, The gene ZNF614 has a mutation status of N385S, The gene LILRB1 has a mutation status of Q401L, The gene NLRP2 has a mutation status of E522G, The gene KMT5C has a mutation status of R9Ter, The gene ZNF584 has a mutation status of Q38L, The gene OTX1 has a mutation status of H276Y, The gene COL6A3 has a mutation status of K2781R, The gene SPATC1L has a mutation status of C325S, The gene SPECC1L has a mutation status of D335E, The gene NF2 has a mutation status of R57Ter, The gene PLXNB2 has a mutation status of F1640del, The gene MAP4 has a mutation status of G1578Ter, The gene FLNB has a mutation status of P631L, The gene PLAAT1 has a mutation status of T54K, The gene MUC4 has a mutation status of V2825A, The gene MUC4 has a mutation status of P2070V, The gene PIGG has a mutation status of E573G, The gene CEP135 has a mutation status of E293D, The gene WWC1 has a mutation status of Y466F, The gene KDM1B has a mutation status of D780E, The gene TDRD6 has a mutation status of G436A, The gene MYO6 has a mutation status of H786LfsTer30, The gene TPD52L1 has a mutation status of V65I, The gene SYNE1 has a mutation status of V1763G, The gene ANKIB1 has a mutation status of S1030R, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of T303V, The gene CDHR3 has a mutation status of P883R, The gene NUGGC has a mutation status of V324I, The gene SDR16C5 has a mutation status of D168G, The gene PREX2 has a mutation status of I636FfsTer8, The gene LRRC69 has a mutation status of P100T, The gene HHLA1 has a mutation status of P484R, The gene PTPRD has a mutation status of E279A, The gene PRSS3 has a mutation status of D102I, The gene P2RY10 has a mutation status of T173S, The gene GUCY2F has a mutation status of S552G	KIPAN
The gene TAS1R3 has a mutation status of W682Ter, The gene TP73 has a mutation status of T143M, The gene HSPG2 has a mutation status of S936P, The gene ZC3H12A has a mutation status of E42G, The gene SPAG17 has a mutation status of E1812K, The gene SV2A has a mutation status of Q323H, The gene POGZ has a mutation status of Q164P, The gene CFAP45 has a mutation status of E539V, The gene ADCY10 has a mutation status of V800I, The gene PRRC2C has a mutation status of M757I, The gene RGSL1 has a mutation status of F877C, The gene RAB3GAP2 has a mutation status of S915P, The gene ACTN2 has a mutation status of G419S, The gene RYR2 has a mutation status of Q3844R, The gene OR2M3 has a mutation status of A216T, The gene MALRD1 has a mutation status of D685A, The gene PTCHD3 has a mutation status of P78AfsTer257, The gene ZNF33A has a mutation status of T744A, The gene BICC1 has a mutation status of H296Y, The gene LRIT1 has a mutation status of N222D, The gene DNMBP has a mutation status of R271Q, The gene PKP3 has a mutation status of Ter798QextTer?, The gene ART1 has a mutation status of F235del, The gene ILK has a mutation status of D330N, The gene NRIP3 has a mutation status of C182S, The gene OR5W2 has a mutation status of M118I, The gene OR8U1 has a mutation status of T106A, The gene B3GNT6 has a mutation status of A74P, The gene SOX5 has a mutation status of P440H, The gene MUC19 has a mutation status of S1602Ter, The gene MUC19 has a mutation status of I6366K, The gene KMT2D has a mutation status of F5199IfsTer43, The gene SLC4A8 has a mutation status of G521R, The gene MYRFL has a mutation status of K262Q, The gene FGD6 has a mutation status of N932S, The gene PCDH17 has a mutation status of E1137D, The gene SLC15A1 has a mutation status of V450I, The gene CARMIL3 has a mutation status of P1084TfsTer11, The gene NEMF has a mutation status of G180D, The gene PIGH has a mutation status of L55Q, The gene ACOT4 has a mutation status of R57C, The gene NRDE2 has a mutation status of R316G, The gene TECPR2 has a mutation status of V947L, The gene DUOX2 has a mutation status of P1391A, The gene ADAMTS17 has a mutation status of G544R, The gene ZNF205 has a mutation status of A545LfsTer51, The gene DHODH has a mutation status of I267V, The gene TP53 has a mutation status of H179Q, The gene MPRIP has a mutation status of G679V, The gene CCL3L3 has a mutation status of P44L, The gene KRT25 has a mutation status of G60V, The gene C17orf113 has a mutation status of V567I, The gene PGS1 has a mutation status of R16P, The gene MC4R has a mutation status of L247M, The gene MFSD12 has a mutation status of T254P, The gene SEMA6B has a mutation status of A872V, The gene ADAMTS10 has a mutation status of D446N, The gene MUC16 has a mutation status of D6322F, The gene OR7A5 has a mutation status of Y259N, The gene OR10H4 has a mutation status of N100H, The gene ZNF257 has a mutation status of C126H, The gene ZNF257 has a mutation status of G128Q, The gene ZNF829 has a mutation status of L367P, The gene ZNF568 has a mutation status of A482LfsTer96, The gene SIX5 has a mutation status of V448A, The gene NTF4 has a mutation status of G122V, The gene ZNF543 has a mutation status of L585F, The gene NT5C1B has a mutation status of R165C, The gene WDPCP has a mutation status of N529K, The gene NCK2 has a mutation status of D12N, The gene LRP1B has a mutation status of I1263T, The gene XIRP2 has a mutation status of M797T, The gene TTN has a mutation status of L33429R, The gene TTN has a mutation status of N1534K, The gene CEP250 has a mutation status of R1401G, The gene CSE1L has a mutation status of Q106K, The gene ZNF217 has a mutation status of E233Ter, The gene BRWD1 has a mutation status of T1805K, The gene TRMU has a mutation status of R93W, The gene PLXNB2 has a mutation status of T931I, The gene HACL1 has a mutation status of Q544H, The gene SCN5A has a mutation status of A425T, The gene SETD2 has a mutation status of Y2023_R2024del, The gene LAMB2 has a mutation status of R119Q, The gene ABHD14A has a mutation status of R245H, The gene CCDC66 has a mutation status of L827F, The gene MAGI1 has a mutation status of A1396T, The gene EFCC1 has a mutation status of R298H, The gene MECOM has a mutation status of T786R, The gene MUC4 has a mutation status of T3942L, The gene POLN has a mutation status of H196R, The gene GABRB1 has a mutation status of T378M, The gene SLAIN2 has a mutation status of S63F, The gene ANKH has a mutation status of L195H, The gene FBXL7 has a mutation status of M279I, The gene LMBRD2 has a mutation status of S302G, The gene DAB2 has a mutation status of K28R, The gene PRDM6 has a mutation status of I548V, The gene MEGF10 has a mutation status of D180E, The gene BRD8 has a mutation status of K1110R, The gene PCDHB4 has a mutation status of D555N, The gene DOK3 has a mutation status of H300Y, The gene MAML1 has a mutation status of N358K, The gene ZNF311 has a mutation status of R343G, The gene OR12D3 has a mutation status of L53I, The gene HLA-F has a mutation status of S351C, The gene MICA has a mutation status of P18R, The gene POU3F2 has a mutation status of G205V, The gene ADGRG6 has a mutation status of T376P, The gene INTS1 has a mutation status of P119L, The gene DNAH11 has a mutation status of E3126D, The gene PCLO has a mutation status of P2351S, The gene SGCE has a mutation status of S249R, The gene BUD31 has a mutation status of Q107P, The gene MUC17 has a mutation status of P1544H, The gene PTPRZ1 has a mutation status of R1624H, The gene UBE3C has a mutation status of W317G, The gene XKR6 has a mutation status of E29D, The gene PNOC has a mutation status of R97Ter, The gene SNAI2 has a mutation status of A173T, The gene TERF1 has a mutation status of R19K, The gene DCAF4L2 has a mutation status of R172H, The gene NECAB1 has a mutation status of V173I, The gene CDC37L1 has a mutation status of E228V, The gene PRSS3 has a mutation status of D102I, The gene PRUNE2 has a mutation status of F402I, The gene PAPPA has a mutation status of E1615del, The gene HMCN2 has a mutation status of D2366E, The gene REXO4 has a mutation status of S40R, The gene SEC16A has a mutation status of L1855F, The gene MT-ND4 has a mutation status of G146D, The gene MT-CYB has a mutation status of M303T, The gene FRMPD4 has a mutation status of V140I, The gene PASD1 has a mutation status of L500_Q506del	STES
The gene FHAD1 has a mutation status of E1137Ter, The gene SEMA6C has a mutation status of S609G, The gene CATSPERE has a mutation status of I380N, The gene SLC29A3 has a mutation status of P114A, The gene CUL5 has a mutation status of Y373C, The gene DLAT has a mutation status of P189Q, The gene ESYT1 has a mutation status of M295I, The gene RASSF3 has a mutation status of Q76K, The gene LEMD3 has a mutation status of R22A, The gene PXN has a mutation status of D949G, The gene CHURC1 has a mutation status of G29S, The gene TTC7B has a mutation status of I839T, The gene ZNF598 has a mutation status of Q616P, The gene ATP2A1 has a mutation status of Y434H, The gene CDH16 has a mutation status of P277RfsTer6, The gene SLC9A5 has a mutation status of E45V, The gene PELP1 has a mutation status of S62P, The gene TP53 has a mutation status of R175H, The gene KRT24 has a mutation status of S517R, The gene DLX4 has a mutation status of E104D, The gene ABCA9 has a mutation status of L255F, The gene PLIN4 has a mutation status of L1344V, The gene SMARCA4 has a mutation status of L639WfsTer7, The gene LILRA2 has a mutation status of W175S, The gene HTRA2 has a mutation status of R104G, The gene EIF2AK3 has a mutation status of V70G, The gene PAX8 has a mutation status of Y245S, The gene OSBPL6 has a mutation status of K755R, The gene FSIP2 has a mutation status of Y1855H, The gene XKR7 has a mutation status of G21C, The gene CTNNB1 has a mutation status of S37A, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene MAML3 has a mutation status of H363P, The gene FAM8A1 has a mutation status of G134I, The gene FAM8A1 has a mutation status of A140T, The gene HLA-DRB5 has a mutation status of Q38W, The gene ITPR3 has a mutation status of S865L, The gene IP6K3 has a mutation status of N172T, The gene CRISP3 has a mutation status of V149I, The gene KHDRBS2 has a mutation status of E170Ter, The gene THBS2 has a mutation status of G225V, The gene HOXA5 has a mutation status of D53N, The gene ORC5 has a mutation status of L80F, The gene KDM7A has a mutation status of G3A, The gene DLGAP2 has a mutation status of N389T, The gene SYBU has a mutation status of P199Q, The gene EEF1D has a mutation status of L291P, The gene MPDZ has a mutation status of E702M, The gene MPDZ has a mutation status of V135G, The gene WHRN has a mutation status of H675Y, The gene C5 has a mutation status of T268HfsTer4, The gene GTF3C5 has a mutation status of G377V, The gene MT-ND4L has a mutation status of M43T, The gene MT-ND4 has a mutation status of T372HfsTer?, The gene CXorf38 has a mutation status of K318_A319delinsNS, The gene NEXMIF has a mutation status of P838S, The gene PASD1 has a mutation status of E385K	OV
The gene NPHP4 has a mutation status of Y1052S, The gene CPLANE2 has a mutation status of G174A, The gene SH2D5 has a mutation status of V167G, The gene HSPG2 has a mutation status of S2294F, The gene A3GALT2 has a mutation status of A273V, The gene KCNQ4 has a mutation status of G64S, The gene PDE4B has a mutation status of S4N, The gene WLS has a mutation status of R405G, The gene DPYD has a mutation status of P393A, The gene NRAS has a mutation status of G13D, The gene IGSF3 has a mutation status of M930T, The gene TENT5C has a mutation status of I94NfsTer16, The gene ADCY10 has a mutation status of H320Y, The gene HMCN1 has a mutation status of L403H, The gene HMCN1 has a mutation status of R5413G, The gene CHI3L1 has a mutation status of I55M, The gene RAB3GAP2 has a mutation status of W1024Ter, The gene ZEB1 has a mutation status of N366S, The gene LIPK has a mutation status of T153K, The gene NHLRC2 has a mutation status of S274L, The gene MCMBP has a mutation status of K429N, The gene NELL1 has a mutation status of Q192Ter, The gene FIBIN has a mutation status of S171F, The gene MYRF has a mutation status of L303P, The gene KDM2A has a mutation status of D486H, The gene ATM has a mutation status of E347K, The gene SORL1 has a mutation status of M335V, The gene KDM5A has a mutation status of K430E, The gene TAS2R19 has a mutation status of L116F, The gene TAS2R31 has a mutation status of F233S, The gene TAS2R46 has a mutation status of I33T, The gene TAS2R30 has a mutation status of I33T, The gene PLEKHA5 has a mutation status of M139V, The gene MUC19 has a mutation status of R6489T, The gene STAB2 has a mutation status of K469M, The gene SART3 has a mutation status of E167Q, The gene ATP12A has a mutation status of E67K, The gene KBTBD6 has a mutation status of A518S, The gene VWA8 has a mutation status of A1693T, The gene DGKH has a mutation status of F211L, The gene RIPK3 has a mutation status of W506Ter, The gene PRKD1 has a mutation status of L617S, The gene SEC23A has a mutation status of P44A, The gene FSCB has a mutation status of E609D, The gene TUNAR has a mutation status of Q31K, The gene IGHV2-70 has a mutation status of G45D, The gene OTUD7A has a mutation status of G558A, The gene MGA has a mutation status of S2981C, The gene CSNK1G1 has a mutation status of R271GfsTer67, The gene KLHL25 has a mutation status of E72D, The gene ACAN has a mutation status of H2299R, The gene ABCA3 has a mutation status of L564V, The gene SLX4 has a mutation status of E971Ter, The gene DNAH3 has a mutation status of Q26Ter, The gene PRSS53 has a mutation status of D412Y, The gene HEATR3 has a mutation status of H49Y, The gene NOB1 has a mutation status of Q344Ter, The gene TCF25 has a mutation status of P227L, The gene INPP5K has a mutation status of P244S, The gene ZNF232 has a mutation status of S15G, The gene MYH13 has a mutation status of G233E, The gene TP53I13 has a mutation status of P159A, The gene GPATCH8 has a mutation status of S510C, The gene MFSD11 has a mutation status of L242F, The gene THEG has a mutation status of D3Y, The gene ARHGEF18 has a mutation status of S555R, The gene UNC13A has a mutation status of E1679D, The gene PRX has a mutation status of S51Ter, The gene MEGF8 has a mutation status of R2220C, The gene PRKD2 has a mutation status of I582T, The gene SYT3 has a mutation status of E6D, The gene ZNF841 has a mutation status of T232A, The gene LILRA1 has a mutation status of P271R, The gene GDF7 has a mutation status of L234M, The gene MTIF2 has a mutation status of A240G, The gene XPO1 has a mutation status of P2A, The gene CHN1 has a mutation status of T174A, The gene TTN has a mutation status of E15947K, The gene SPATS2L has a mutation status of E295K, The gene SCYGR2 has a mutation status of H97S, The gene SLC19A3 has a mutation status of D480N, The gene GIGYF2 has a mutation status of N91K, The gene PPP1R16B has a mutation status of W445C, The gene FAM210B has a mutation status of P20T, The gene OGFR has a mutation status of R565_P584del, The gene COL6A2 has a mutation status of E311Ter, The gene NPRL2 has a mutation status of R311G, The gene DNAH1 has a mutation status of Y892H, The gene DZIP3 has a mutation status of D704N, The gene TLL1 has a mutation status of S447N, The gene ICE1 has a mutation status of S1599R, The gene ANXA2R has a mutation status of E106Q, The gene CCDC112 has a mutation status of R351T, The gene PCDHB7 has a mutation status of S631G, The gene PCDHGB4 has a mutation status of C753Y, The gene DIAPH1 has a mutation status of N1054K, The gene IRGM has a mutation status of E24SfsTer10, The gene IRGM has a mutation status of L26_K27del, The gene ATP10B has a mutation status of Q1440RfsTer20, The gene RIPK1 has a mutation status of A569V, The gene DSP has a mutation status of L143V, The gene HLA-DQA2 has a mutation status of S75R, The gene UBE3D has a mutation status of S113F, The gene PRDM13 has a mutation status of P600L, The gene DDO has a mutation status of F38SfsTer6, The gene MAP3K5 has a mutation status of G692W, The gene RSPH3 has a mutation status of I288T, The gene TARP has a mutation status of P6L, The gene TRGV3 has a mutation status of G34DfsTer22, The gene AGAP3 has a mutation status of V610L, The gene PRKDC has a mutation status of H1175Y, The gene RP1 has a mutation status of V1498A, The gene LRRCC1 has a mutation status of E38Ter, The gene CNGB3 has a mutation status of T83I, The gene CSMD3 has a mutation status of G3W, The gene FOCAD has a mutation status of N507D, The gene IARS1 has a mutation status of S35P, The gene MIGA2 has a mutation status of T218S, The gene MT-ND1 has a mutation status of A147T, The gene MT-ND4 has a mutation status of K93NfsTer?, The gene MT-CYB has a mutation status of H16R, The gene MXRA5 has a mutation status of G1654E, The gene ZNF157 has a mutation status of E390Q, The gene ZNF157 has a mutation status of E411K, The gene HCFC1 has a mutation status of A1804T	DLBC
The gene PRKCZ has a mutation status of D227N, The gene TRIM63 has a mutation status of E108K, The gene TMEM61 has a mutation status of S176R, The gene C8B has a mutation status of R83M, The gene CLCA4 has a mutation status of S735Y, The gene TAFA3 has a mutation status of E6Q, The gene SLC25A44 has a mutation status of S228L, The gene METTL13 has a mutation status of Q163Ter, The gene EXOC6 has a mutation status of M244V, The gene PRPF19 has a mutation status of D54V, The gene NUMA1 has a mutation status of E458K, The gene ARHGEF17 has a mutation status of P26L, The gene SCNN1A has a mutation status of R181W, The gene IGHM has a mutation status of E299K, The gene KLF13 has a mutation status of S287L, The gene MAPK3 has a mutation status of R15S, The gene MAPK3 has a mutation status of G12V, The gene SLC9A5 has a mutation status of Y609H, The gene CFDP1 has a mutation status of E112Q, The gene DNAH17 has a mutation status of A3696S, The gene MC4R has a mutation status of K314E, The gene SALL3 has a mutation status of A185L, The gene SALL3 has a mutation status of P1039T, The gene SMARCA4 has a mutation status of Q555Ter, The gene SIPA1L3 has a mutation status of G1346SfsTer57, The gene KIR2DL4 has a mutation status of S282T, The gene KIR2DS4 has a mutation status of A168G, The gene KIR2DS4 has a mutation status of A169P, The gene PCARE has a mutation status of Q1020R, The gene TMEM131 has a mutation status of S989P, The gene MAP4K4 has a mutation status of R459W, The gene ABCB6 has a mutation status of V609L, The gene MAVS has a mutation status of H453P, The gene TATDN2 has a mutation status of R67W, The gene EAF1 has a mutation status of S45C, The gene FBXL2 has a mutation status of L188P, The gene KPNA4 has a mutation status of E5Ter, The gene FAT1 has a mutation status of C4151Ter, The gene RXFP3 has a mutation status of H426N, The gene C7 has a mutation status of T543I, The gene PURA has a mutation status of G38V, The gene SPDL1 has a mutation status of R453S, The gene DOCK2 has a mutation status of K835E, The gene OR2V1 has a mutation status of S88Y, The gene HLA-A has a mutation status of Y137N, The gene SYNE1 has a mutation status of I7873T, The gene TNRC18 has a mutation status of L56R, The gene CCDC201 has a mutation status of P18T, The gene FGL2 has a mutation status of R329C, The gene ATXN7L1 has a mutation status of P716L, The gene LMOD2 has a mutation status of H251Q, The gene CUL1 has a mutation status of Q509H, The gene GDF6 has a mutation status of G89S, The gene VPS13B has a mutation status of R1143Q, The gene PARP10 has a mutation status of C876DfsTer75, The gene MPDZ has a mutation status of E702M, The gene MT-CO3 has a mutation status of F235L, The gene MT-ND5 has a mutation status of T533M, The gene ABCB7 has a mutation status of S261G	SARC
The gene PRAMEF11 has a mutation status of V27I, The gene PRAMEF11 has a mutation status of A15V, The gene KLHDC7A has a mutation status of E749M, The gene MACF1 has a mutation status of L4032del, The gene CENPF has a mutation status of E1605Ter, The gene OPTN has a mutation status of R482_E483delinsK, The gene PARD3 has a mutation status of G901R, The gene SAMD8 has a mutation status of V290G, The gene CDKN1C has a mutation status of A134S, The gene OR4A5 has a mutation status of G39W, The gene RNF169 has a mutation status of E364D, The gene EED has a mutation status of P10S, The gene CASP5 has a mutation status of I114T, The gene C2CD2L has a mutation status of E178D, The gene OR10G8 has a mutation status of S92A, The gene COL2A1 has a mutation status of P1368A, The gene NAV3 has a mutation status of L1511V, The gene PAH has a mutation status of E44D, The gene SCFD1 has a mutation status of K381TfsTer6, The gene INSM2 has a mutation status of E50G, The gene RTN1 has a mutation status of E362Q, The gene BUB1B has a mutation status of T620S, The gene PKD1 has a mutation status of V2267G, The gene NTAN1 has a mutation status of H115Y, The gene MVP has a mutation status of G269A, The gene MT1A has a mutation status of G52E, The gene TERF2 has a mutation status of Q475R, The gene TP53 has a mutation status of A119QfsTer5, The gene CHD3 has a mutation status of Q386E, The gene KRT31 has a mutation status of N255K, The gene KAT2A has a mutation status of P302L, The gene CBX4 has a mutation status of H400du, The gene ZBTB14 has a mutation status of F4L, The gene RAB12 has a mutation status of F11L, The gene SETBP1 has a mutation status of P1536T, The gene ANGPTL4 has a mutation status of A92V, The gene S1PR2 has a mutation status of A230D, The gene PSG7 has a mutation status of N268H, The gene ERCC2 has a mutation status of R185Q, The gene LILRB1 has a mutation status of Q401L, The gene NLRP7 has a mutation status of A854D, The gene SLC1A4 has a mutation status of L93P, The gene MERTK has a mutation status of P7L, The gene STEAP3 has a mutation status of F331SfsTer56, The gene XIRP2 has a mutation status of P2699R, The gene TTN has a mutation status of E15117K, The gene TTN has a mutation status of K15002Q, The gene ADAM23 has a mutation status of G5C, The gene TRIP12 has a mutation status of G493E, The gene OVOL2 has a mutation status of Q202Ter, The gene BPIFA2 has a mutation status of D34G, The gene SPECC1L has a mutation status of S1037LfsTer7, The gene SFI1 has a mutation status of T397N, The gene DEPDC5 has a mutation status of F77L, The gene ZCWPW2 has a mutation status of Q83R, The gene KLHL18 has a mutation status of E3A, The gene BSN has a mutation status of Q136HfsTer76, The gene SI has a mutation status of L652I, The gene PDCD10 has a mutation status of Ter213WextTer25, The gene SPON2 has a mutation status of A105E, The gene FRAS1 has a mutation status of T3618I, The gene NIPBL has a mutation status of L1978I, The gene UBTD2 has a mutation status of G6D, The gene RING1 has a mutation status of G217V, The gene TRERF1 has a mutation status of E999Ter, The gene LGSN has a mutation status of R366Ter, The gene L3MBTL3 has a mutation status of G223V, The gene GPER1 has a mutation status of E218P, The gene CCL26 has a mutation status of K67R, The gene PCLO has a mutation status of F2639L, The gene PCLO has a mutation status of T439S, The gene MUC3A has a mutation status of E725K, The gene PLXNA4 has a mutation status of S1630I, The gene DGKI has a mutation status of Q111H, The gene BRAF has a mutation status of V600E, The gene PRKAG2 has a mutation status of S226C, The gene DLGAP2 has a mutation status of N389T, The gene SPIDR has a mutation status of S286P, The gene SNX16 has a mutation status of R170C, The gene C8orf76 has a mutation status of H207R, The gene CDKN2B has a mutation status of E16D, The gene TTLL11 has a mutation status of A34Ter, The gene SNAPC4 has a mutation status of P914T, The gene MT-ND5 has a mutation status of T13A, The gene MT-ND6 has a mutation status of V106A, The gene MT-ND6 has a mutation status of F19L, The gene IL13RA1 has a mutation status of F287S	SARC
The gene MMP23B has a mutation status of R377H, The gene EXTL1 has a mutation status of R544K, The gene MTF1 has a mutation status of T703A, The gene GPR88 has a mutation status of G249D, The gene TTF2 has a mutation status of N270Y, The gene LCE1F has a mutation status of G65C, The gene ARHGEF11 has a mutation status of M1320RfsTer44, The gene IL19 has a mutation status of C18Ter, The gene ESRRG has a mutation status of L79P, The gene FRA10AC1 has a mutation status of Q75Ter, The gene GPAM has a mutation status of C490F, The gene EMX2 has a mutation status of P91QfsTer78, The gene EMX2 has a mutation status of H92TfsTer76, The gene CPXM2 has a mutation status of S347G, The gene OR52J3 has a mutation status of L68I, The gene DCHS1 has a mutation status of A2963D, The gene IPO7 has a mutation status of N803S, The gene DCDC1 has a mutation status of E437D, The gene RAB3IL1 has a mutation status of T163M, The gene AIP has a mutation status of R81Ter, The gene NXPE4 has a mutation status of L39V, The gene TAS2R31 has a mutation status of I33T, The gene MUC19 has a mutation status of T3551A, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene MUC19 has a mutation status of N4824T, The gene DDX23 has a mutation status of S41P, The gene LRRIQ1 has a mutation status of H1090L, The gene CEP83 has a mutation status of E443V, The gene NOS1 has a mutation status of E1054Q, The gene PARP4 has a mutation status of K1239N, The gene FREM2 has a mutation status of P1704T, The gene NALCN has a mutation status of P1191T, The gene HECTD1 has a mutation status of G347R, The gene POLE2 has a mutation status of L11F, The gene FERMT2 has a mutation status of T192N, The gene TMEM30B has a mutation status of A166T, The gene SYNE2 has a mutation status of I526T, The gene CATSPERB has a mutation status of M901I, The gene ATP10A has a mutation status of G349V, The gene TRPM1 has a mutation status of G305E, The gene PLCB2 has a mutation status of A395V, The gene FBN1 has a mutation status of I849V, The gene TP53 has a mutation status of R273C, The gene L3MBTL4 has a mutation status of M409I, The gene IMPACT has a mutation status of L104R, The gene SMIM21 has a mutation status of W78R, The gene MIDN has a mutation status of P368LfsTer200, The gene MRPL54 has a mutation status of R128H, The gene ZNF557 has a mutation status of Y348C, The gene MUC16 has a mutation status of D3437Y, The gene SLC1A6 has a mutation status of E528D, The gene ZNF493 has a mutation status of D597_K598delinsEE, The gene SYCN has a mutation status of S32_D33insRL, The gene ZNF227 has a mutation status of D142N, The gene LILRA6 has a mutation status of Q350_F351insGY, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of Q401L, The gene GPN1 has a mutation status of S364L, The gene PSME4 has a mutation status of M1720T, The gene DNAH6 has a mutation status of S1266G, The gene EIF2AK3 has a mutation status of E1050K, The gene ITGB6 has a mutation status of P206R, The gene TTN has a mutation status of A35263F, The gene DNAH7 has a mutation status of G3455DfsTer18, The gene AGAP1 has a mutation status of Ter858LextTer27, The gene LZTS3 has a mutation status of P314Q, The gene TOP1 has a mutation status of K184E, The gene LRRC75B has a mutation status of Y73C, The gene SERHL2 has a mutation status of M309L, The gene SGO1 has a mutation status of D380E, The gene USP4 has a mutation status of G73V, The gene SLC38A3 has a mutation status of E56K, The gene ACOX2 has a mutation status of M81T, The gene PTPRG has a mutation status of R432H, The gene HEG1 has a mutation status of G1345V, The gene GFM1 has a mutation status of T369CfsTer12, The gene TMEM150C has a mutation status of E236G, The gene FAT4 has a mutation status of S4458P, The gene TMEM131L has a mutation status of L498V, The gene FGG has a mutation status of D314EfsTer51, The gene FAT1 has a mutation status of L2449I, The gene ARL15 has a mutation status of I77V, The gene PCDHB10 has a mutation status of S68Y, The gene JAKMIP2 has a mutation status of Q797K, The gene ARSI has a mutation status of V175M, The gene KCNIP1 has a mutation status of E28Ter, The gene RIPK1 has a mutation status of A569V, The gene OR2B8P has a mutation status of W51S, The gene DDR1 has a mutation status of D795E, The gene PHF3 has a mutation status of K668R, The gene SYNE1 has a mutation status of V4348M, The gene LPA has a mutation status of S1395G, The gene AGMO has a mutation status of A358G, The gene HDAC9 has a mutation status of G712R, The gene MUC3A has a mutation status of W18G, The gene RELN has a mutation status of H1325Y, The gene CNTNAP2 has a mutation status of K710T, The gene CRYGN has a mutation status of P55_D56del, The gene ADGRA2 has a mutation status of E1245G, The gene ZFHX4 has a mutation status of L27R, The gene SLC7A13 has a mutation status of S126R, The gene TMEM64 has a mutation status of C315LfsTer30, The gene LYNX1 has a mutation status of L12F, The gene CCL27 has a mutation status of D61E, The gene SECISBP2 has a mutation status of N187S, The gene PHF2 has a mutation status of R201P, The gene ERCC6L2 has a mutation status of R1068I, The gene MT-CO3 has a mutation status of G234S, The gene VCX3A has a mutation status of S108A, The gene KLHL13 has a mutation status of F529V, The gene ACTRT1 has a mutation status of F363L, The gene PNMA6E has a mutation status of G636R	DLBC
The gene TRIM63 has a mutation status of S110C, The gene ZDHHC18 has a mutation status of D371Y, The gene CLCA1 has a mutation status of A819V, The gene CLCA4 has a mutation status of I612M, The gene STRIP1 has a mutation status of Q30H, The gene NRAS has a mutation status of Q61K, The gene CELF3 has a mutation status of G324V, The gene KCNN3 has a mutation status of P63Q, The gene HMCN1 has a mutation status of Q760R, The gene ASPM has a mutation status of A22P, The gene OBSCN has a mutation status of A5522D, The gene TRIM67 has a mutation status of A61VfsTer234, The gene OR2L13 has a mutation status of G218C, The gene GAD2 has a mutation status of M204T, The gene LMNTD2 has a mutation status of H301P, The gene OR56B2P has a mutation status of H63P, The gene SLC17A6 has a mutation status of A224T, The gene CLPB has a mutation status of D222N, The gene KLHL35 has a mutation status of T420P, The gene NRIP2 has a mutation status of L192R, The gene TAPBPL has a mutation status of D44G, The gene SLCO1A2 has a mutation status of Y221Ter, The gene MUC19 has a mutation status of I6366K, The gene DBX2 has a mutation status of G337W, The gene H1-7 has a mutation status of S19G, The gene PXN has a mutation status of T251P, The gene KNTC1 has a mutation status of I741V, The gene TMEM132B has a mutation status of P878H, The gene ADPRHL1 has a mutation status of G1442C, The gene DHRS4L2 has a mutation status of E94G, The gene CHGA has a mutation status of E362G, The gene IGHV3-74 has a mutation status of L30F, The gene FOXB1 has a mutation status of T300P, The gene KBTBD13 has a mutation status of D290A, The gene WDR90 has a mutation status of P1013L, The gene MSLNL has a mutation status of G278R, The gene SETD1A has a mutation status of H749P, The gene PRSS36 has a mutation status of D488A, The gene MON1B has a mutation status of E320GfsTer119, The gene ITGAE has a mutation status of S918P, The gene KIF1C has a mutation status of V12G, The gene CFAP52 has a mutation status of N66K, The gene LIG3 has a mutation status of T219S, The gene FBXL20 has a mutation status of V280G, The gene KRTAP17-1 has a mutation status of G33R, The gene KRT32 has a mutation status of P427I, The gene PLEKHM1 has a mutation status of A546G, The gene SMIM36 has a mutation status of S79Y, The gene ENPP7 has a mutation status of T68P, The gene ENDOV has a mutation status of V78G, The gene ACTG1 has a mutation status of F90del, The gene ZNF521 has a mutation status of V284I, The gene KCTD1 has a mutation status of R844P, The gene ASXL3 has a mutation status of I1279K, The gene DIRAS1 has a mutation status of V18G, The gene TLE2 has a mutation status of P209R, The gene MUC16 has a mutation status of E583K, The gene ZNF560 has a mutation status of L134M, The gene COL5A3 has a mutation status of F454L, The gene PDE4A has a mutation status of D517A, The gene WDR62 has a mutation status of I1268L, The gene RINL has a mutation status of P12T, The gene PRX has a mutation status of P456S, The gene PNMA8B has a mutation status of V397G, The gene FAM83E has a mutation status of V231G, The gene IGLON5 has a mutation status of S30P, The gene TRMT61B has a mutation status of S69Y, The gene PKDCC has a mutation status of H194P, The gene SOWAHC has a mutation status of G224D, The gene FBLN7 has a mutation status of R238PfsTer27, The gene GALNT13 has a mutation status of L114I, The gene KCNJ3 has a mutation status of S69P, The gene SCN2A has a mutation status of V892I, The gene IDH1 has a mutation status of R132C, The gene CPXM1 has a mutation status of L348R, The gene NKX2-4 has a mutation status of Y137D, The gene ACSS1 has a mutation status of A70DfsTer80, The gene SRC has a mutation status of L18R, The gene IGLV2-18 has a mutation status of R53S, The gene AP1B1 has a mutation status of D657Y, The gene CCR5 has a mutation status of L39V, The gene PRSS50 has a mutation status of W124G, The gene COL7A1 has a mutation status of T1231I, The gene NCKIPSD has a mutation status of P551S, The gene BSN has a mutation status of S3450R, The gene TFDP2 has a mutation status of V159L, The gene SH3BP2 has a mutation status of R292Q, The gene WFS1 has a mutation status of Q520Ter, The gene SOD3 has a mutation status of H139P, The gene SOD3 has a mutation status of H142P, The gene FREM3 has a mutation status of F723L, The gene SORBS2 has a mutation status of K413SfsTer24, The gene RICTOR has a mutation status of N1128QfsTer13, The gene GFRA3 has a mutation status of M349I, The gene MGAT4B has a mutation status of H111P, The gene RPP21 has a mutation status of V5G, The gene TAF8 has a mutation status of E63Q, The gene AARS2 has a mutation status of R166W, The gene HINT3 has a mutation status of N68S, The gene SOGA3 has a mutation status of A127P, The gene MICALL2 has a mutation status of L242P, The gene RAC1 has a mutation status of N92I, The gene HYCC1 has a mutation status of Y272H, The gene CAMK2B has a mutation status of P476RfsTer9, The gene FLNC has a mutation status of V215WfsTer37, The gene KDM7A has a mutation status of V8G, The gene RBM33 has a mutation status of Q596H, The gene ANGPT1 has a mutation status of I419T, The gene HGH1 has a mutation status of V159G, The gene MT-ND4 has a mutation status of I165T, The gene ARHGAP6 has a mutation status of T963S, The gene FAM47B has a mutation status of R114P, The gene NKAP has a mutation status of S36P, The gene SPANXN4 has a mutation status of K29del	SARC
The gene ZSWIM5 has a mutation status of H1156R, The gene LRRIQ3 has a mutation status of M569K, The gene LRRIQ3 has a mutation status of E568K, The gene NBPF12 has a mutation status of E80Ter, The gene FCRL5 has a mutation status of S530C, The gene METTL18 has a mutation status of V191SfsTer29, The gene WDR64 has a mutation status of T894I, The gene GPRIN2 has a mutation status of L428V, The gene ERCC6 has a mutation status of P1095A, The gene OR4C12 has a mutation status of R301K, The gene TRIM77 has a mutation status of V345M, The gene PHLDB1 has a mutation status of S638R, The gene ENO2 has a mutation status of D297Y, The gene TDG has a mutation status of L265_Y267du, The gene TXNRD1 has a mutation status of N152S, The gene TCHP has a mutation status of Q384E, The gene ALDH6A1 has a mutation status of A132G, The gene DIO2 has a mutation status of A195S, The gene HSP90AA1 has a mutation status of K147N, The gene AHNAK2 has a mutation status of L4169H, The gene FMN1 has a mutation status of P209S, The gene ITGA11 has a mutation status of M803I, The gene ADAMTS7 has a mutation status of W1379G, The gene ADAMTS7 has a mutation status of M610I, The gene CAPN15 has a mutation status of M1?, The gene VAT1L has a mutation status of Y307D, The gene PKD1L2 has a mutation status of T1446K, The gene GPS2 has a mutation status of Y164Ter, The gene TP53 has a mutation status of C135F, The gene TEKT3 has a mutation status of D209E, The gene KSR1 has a mutation status of E764K, The gene MEIOC has a mutation status of A414V, The gene NOL11 has a mutation status of A656V, The gene GRIN3B has a mutation status of L147M, The gene LONP1 has a mutation status of M569I, The gene MUC16 has a mutation status of S13600I, The gene ZNF536 has a mutation status of P1261R, The gene RHPN2 has a mutation status of A29V, The gene PRKD2 has a mutation status of Q165E, The gene ZSWIM9 has a mutation status of C810F, The gene AP2A1 has a mutation status of E949D, The gene KIR2DL1 has a mutation status of N144S, The gene TET3 has a mutation status of A71T, The gene AFF3 has a mutation status of I305T, The gene ARHGEF4 has a mutation status of D139EfsTer134, The gene RAB3GAP1 has a mutation status of N382D, The gene NYAP2 has a mutation status of S638T, The gene NCL has a mutation status of G594S, The gene SEL1L2 has a mutation status of H640Y, The gene SCARF2 has a mutation status of V61L, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene TMEM43 has a mutation status of E142Q, The gene PLXND1 has a mutation status of A63T, The gene COL6A5 has a mutation status of A1868S, The gene GNB4 has a mutation status of R46L, The gene KIT has a mutation status of D737H, The gene MTHFD2L has a mutation status of S45N, The gene BASP1 has a mutation status of A137T, The gene CPLANE1 has a mutation status of P728A, The gene EDIL3 has a mutation status of S375Ter, The gene CCNG1 has a mutation status of Y161C, The gene C5orf47 has a mutation status of E9K, The gene SLC17A4 has a mutation status of C223Ter, The gene HLA-B has a mutation status of A93R, The gene HLA-B has a mutation status of I90K, The gene HLA-DRB1 has a mutation status of S66N, The gene COL19A1 has a mutation status of I178M, The gene FILIP1 has a mutation status of D797Y, The gene CRYBG1 has a mutation status of K845N, The gene MFSD4B has a mutation status of L182Y, The gene AHI1 has a mutation status of R235K, The gene AIG1 has a mutation status of S154L, The gene MTHFD1L has a mutation status of A467S, The gene CCDC170 has a mutation status of A597S, The gene SNX9 has a mutation status of I506V, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene MUC3A has a mutation status of S2495L, The gene PTK2B has a mutation status of P724S, The gene CYP7B1 has a mutation status of G44D, The gene MT-ND6 has a mutation status of V31A, The gene PPP1R3F has a mutation status of L699del, The gene SLC25A5 has a mutation status of T221R, The gene MAGEC1 has a mutation status of H795P	GBMLGG
The gene MIB2 has a mutation status of N283T, The gene CHD5 has a mutation status of G1077S, The gene TMEM69 has a mutation status of G194R, The gene ADGRL2 has a mutation status of L1060F, The gene LRIG2 has a mutation status of T545I, The gene CD101 has a mutation status of N648T, The gene IGSF9 has a mutation status of E150A, The gene METTL18 has a mutation status of S148QfsTer10, The gene ETNK2 has a mutation status of V222G, The gene KLHDC8A has a mutation status of L309F, The gene SYT14 has a mutation status of S516P, The gene USH2A has a mutation status of N2334H, The gene C1orf131 has a mutation status of K240T, The gene HNRNPU has a mutation status of Q176Ter, The gene CREM has a mutation status of T162P, The gene FZD8 has a mutation status of T157P, The gene OGDHL has a mutation status of F670L, The gene ZNF503 has a mutation status of D382A, The gene PITX3 has a mutation status of A162P, The gene LMNTD2 has a mutation status of K103Q, The gene MUC5AC has a mutation status of P2368_A2375del, The gene MUC5AC has a mutation status of A5353K, The gene ELP4 has a mutation status of I360V, The gene TRIM51G has a mutation status of D207V, The gene OR5AN1 has a mutation status of P22S, The gene MRPL16 has a mutation status of S27I, The gene PPP2R5B has a mutation status of A70V, The gene TYR has a mutation status of Y156C, The gene ARID2 has a mutation status of Y546C, The gene C1QL4 has a mutation status of Y236S, The gene FBRSL1 has a mutation status of R154I, The gene BRCA2 has a mutation status of V3079L, The gene IRS2 has a mutation status of S984I, The gene TRAV30 has a mutation status of F108L, The gene AKAP6 has a mutation status of K1909N, The gene NKX2-8 has a mutation status of L90V, The gene HEATR4 has a mutation status of E863Ter, The gene GSC has a mutation status of A229V, The gene IGHV2-70D has a mutation status of F79L, The gene ATP10A has a mutation status of C55G, The gene ZNF106 has a mutation status of S579F, The gene ARID3B has a mutation status of T408P, The gene ADCY9 has a mutation status of P776H, The gene MYLK3 has a mutation status of G524C, The gene NOB1 has a mutation status of E5G, The gene CRISPLD2 has a mutation status of Y373N, The gene IRF8 has a mutation status of Q118K, The gene IRF8 has a mutation status of C120R, The gene USP22 has a mutation status of K421Ter, The gene NLK has a mutation status of P41del, The gene IKZF3 has a mutation status of N160S, The gene IGFBP4 has a mutation status of T71P, The gene PPM1E has a mutation status of E94D, The gene GNA13 has a mutation status of Y89Ter, The gene CCDC40 has a mutation status of R1006H, The gene CABLES1 has a mutation status of Q265P, The gene PLIN4 has a mutation status of L1344V, The gene ZNF426 has a mutation status of R255G, The gene F2RL3 has a mutation status of G3W, The gene SLC5A5 has a mutation status of G492V, The gene UBA52 has a mutation status of R42C, The gene ZNF676 has a mutation status of G261_K316del, The gene WDR87 has a mutation status of G181V, The gene RYR1 has a mutation status of T1307P, The gene ZC3H4 has a mutation status of H853P, The gene SOX11 has a mutation status of T302P, The gene GALNT14 has a mutation status of R6P, The gene IGKJ1 has a mutation status of T3SfsTer?, The gene IGKJ1 has a mutation status of W2CfsTer?, The gene TTN has a mutation status of V2919L, The gene NABP1 has a mutation status of T144S, The gene ZDBF2 has a mutation status of S1112R, The gene GLB1L has a mutation status of K140E, The gene HJURP has a mutation status of G160D, The gene ANKMY1 has a mutation status of S222I, The gene PLAGL2 has a mutation status of Y342H, The gene NCOA6 has a mutation status of Q704K, The gene RALGAPB has a mutation status of G1171A, The gene EEF1A2 has a mutation status of S416P, The gene KRTAP19-5 has a mutation status of S57G, The gene COL18A1 has a mutation status of T400P, The gene IGLV3-21 has a mutation status of Y67C, The gene IGLV2-11 has a mutation status of G16E, The gene IGLV2-11 has a mutation status of N90D, The gene BCR has a mutation status of S69T, The gene TRIOBP has a mutation status of G2270V, The gene CACNA1D has a mutation status of R85C, The gene ASB14 has a mutation status of L333F, The gene CRYBG3 has a mutation status of Q1953H, The gene MIX23 has a mutation status of M23I, The gene TPRA1 has a mutation status of E143G, The gene IDUA has a mutation status of T366P, The gene NKX6-1 has a mutation status of P20S, The gene MYOZ2 has a mutation status of V223D, The gene NEK1 has a mutation status of L850R, The gene FAM149A has a mutation status of D596G, The gene EGFLAM has a mutation status of H967R, The gene MROH2B has a mutation status of P346L, The gene ANKDD1B has a mutation status of L287V, The gene SH3PXD2B has a mutation status of Q52H, The gene RREB1 has a mutation status of E62del, The gene CCND3 has a mutation status of I290T, The gene DNAH11 has a mutation status of G2236V, The gene AUTS2 has a mutation status of T957P, The gene TBL2 has a mutation status of A34G, The gene SPACDR has a mutation status of S117C, The gene LRCH4 has a mutation status of A473P, The gene MUC12 has a mutation status of M5244K, The gene COL26A1 has a mutation status of Y37S, The gene CDHR3 has a mutation status of D414G, The gene UBN2 has a mutation status of Q118L, The gene FMC1 has a mutation status of Q81K, The gene NEFM has a mutation status of S46P, The gene BHLHE22 has a mutation status of V110G, The gene RDH10 has a mutation status of V38G, The gene MYC has a mutation status of L164V, The gene MROH5 has a mutation status of S29Y, The gene PLEC has a mutation status of L3873M, The gene GALT has a mutation status of P66S, The gene ARHGEF39 has a mutation status of R244Q, The gene HSDL2 has a mutation status of I332L, The gene SNX30 has a mutation status of A69V, The gene MAN1B1 has a mutation status of R159K, The gene MT-ND6 has a mutation status of T159M, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene PPP2R3B has a mutation status of V273M, The gene WWC3 has a mutation status of G631V, The gene DCAF8L2 has a mutation status of E132_E147del, The gene RPGR has a mutation status of E6Q, The gene GLOD5 has a mutation status of I158T, The gene MED12 has a mutation status of V41E, The gene PHKA1 has a mutation status of Y104C, The gene KLHL4 has a mutation status of R360Ter	DLBC
The gene C1orf167 has a mutation status of G192W, The gene HNRNPCL2 has a mutation status of K230T, The gene HTR6 has a mutation status of C205W, The gene CEP85 has a mutation status of Q580K, The gene GBP6 has a mutation status of E550Q, The gene TSHB has a mutation status of R34T, The gene SLC22A15 has a mutation status of V3G, The gene GOLPH3L has a mutation status of S206N, The gene OR6K3 has a mutation status of M101T, The gene TIPRL has a mutation status of V104F, The gene NIBAN1 has a mutation status of W167L, The gene PRELP has a mutation status of L368M, The gene OBSCN has a mutation status of G379R, The gene MTR has a mutation status of R29G, The gene KIFBP has a mutation status of Y128D, The gene CHST3 has a mutation status of N249T, The gene NEURL1 has a mutation status of A368D, The gene DOCK1 has a mutation status of I295M, The gene C2CD3 has a mutation status of N1746K, The gene KDM4E has a mutation status of N29D, The gene ARHGEF12 has a mutation status of T1293K, The gene SORL1 has a mutation status of Q2007R, The gene IQSEC3 has a mutation status of Y632C, The gene PIK3C2G has a mutation status of E643Ter, The gene NACA has a mutation status of N2071S, The gene KCTD10 has a mutation status of E2K, The gene EXOSC8 has a mutation status of K237N, The gene OXGR1 has a mutation status of I55T, The gene PPP4R4 has a mutation status of K375N, The gene CCDC85C has a mutation status of A157T, The gene FMN1 has a mutation status of S272A, The gene STARD9 has a mutation status of W4249C, The gene DPP8 has a mutation status of R477Ter, The gene RASGRF1 has a mutation status of K21R, The gene PLIN1 has a mutation status of S440P, The gene PKD1 has a mutation status of I3367M, The gene PAQR4 has a mutation status of H18Y, The gene PKD1L2 has a mutation status of L711P, The gene OR1P1 has a mutation status of D33A, The gene TP53 has a mutation status of P47RfsTer76, The gene GPR179 has a mutation status of D782A, The gene ACLY has a mutation status of A470P, The gene AOC2 has a mutation status of L160P, The gene PRKAR1A has a mutation status of I255RfsTer13, The gene FBF1 has a mutation status of A919G, The gene SKOR2 has a mutation status of H280P, The gene APC2 has a mutation status of T1264I, The gene MAN2B1 has a mutation status of T452P, The gene LSR has a mutation status of F214L, The gene ZNF585B has a mutation status of F643I, The gene IFNL2 has a mutation status of H132Y, The gene FCGBP has a mutation status of T1234_L1242del, The gene COQ8B has a mutation status of V213G, The gene ZNF28 has a mutation status of K290R, The gene KIR2DL1 has a mutation status of S205A, The gene PPP6R1 has a mutation status of M57I, The gene ZNF835 has a mutation status of R279H, The gene ZNF550 has a mutation status of H66Q, The gene ZNF586 has a mutation status of S300R, The gene TAF1B has a mutation status of S323N, The gene KCNS3 has a mutation status of A184T, The gene TRABD2A has a mutation status of S2N, The gene ANKRD23 has a mutation status of S11N, The gene ABI2 has a mutation status of I38V, The gene FZD5 has a mutation status of R532L, The gene ASB18 has a mutation status of A327G, The gene NOP56 has a mutation status of E107K, The gene BFSP1 has a mutation status of R283Q, The gene WDR4 has a mutation status of G221A, The gene PCNT has a mutation status of E638D, The gene C22orf23 has a mutation status of G15R, The gene CRELD2 has a mutation status of S295A, The gene P4HTM has a mutation status of T137P, The gene MUC4 has a mutation status of A4086T, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene MUC4 has a mutation status of P1378H, The gene MUC4 has a mutation status of P1218L, The gene DGKQ has a mutation status of T418I, The gene TACC3 has a mutation status of D192N, The gene TNIP2 has a mutation status of R229H, The gene ARHGAP24 has a mutation status of K195T, The gene ADCY2 has a mutation status of I92V, The gene MCTP1 has a mutation status of H128L, The gene NMUR2 has a mutation status of V206D, The gene BMP6 has a mutation status of G193S, The gene RPP21 has a mutation status of V5G, The gene RPP21 has a mutation status of R8P, The gene SASH1 has a mutation status of D663GfsTer4, The gene SASH1 has a mutation status of L667_E670del, The gene AKAP12 has a mutation status of G221E, The gene CYP2W1 has a mutation status of R73C, The gene NPC1L1 has a mutation status of C78S, The gene GNAT3 has a mutation status of D133H, The gene GPR22 has a mutation status of I174F, The gene ATP6V1F has a mutation status of R4G, The gene CRISPLD1 has a mutation status of W124R, The gene MATN2 has a mutation status of T276I, The gene OXR1 has a mutation status of F213L, The gene PSIP1 has a mutation status of G279Ter, The gene CAAP1 has a mutation status of E267G, The gene PCSK5 has a mutation status of Q1382L, The gene TEX10 has a mutation status of H278R, The gene GPR21 has a mutation status of W154Ter, The gene ABCA2 has a mutation status of A1451P, The gene MT-ND4L has a mutation status of T13A, The gene MT-ND5 has a mutation status of T533M, The gene MT-CYB has a mutation status of A29T, The gene CXorf38 has a mutation status of P105R, The gene PCSK1N has a mutation status of S4A, The gene EZHIP has a mutation status of A267P, The gene IQSEC2 has a mutation status of L430V, The gene MAGEH1 has a mutation status of R124C, The gene ASB12 has a mutation status of L226P, The gene MED12 has a mutation status of E881D, The gene GPRASP1 has a mutation status of F815C, The gene ADGRG4 has a mutation status of S482F, The gene ZNF185 has a mutation status of A404V, The gene PDZD4 has a mutation status of T519P, The gene DKC1 has a mutation status of I163T	THCA
The gene BMP8B has a mutation status of G92S, The gene PTPRF has a mutation status of P458A, The gene LEPR has a mutation status of A967V, The gene RPL5 has a mutation status of Q122Ter, The gene CELSR2 has a mutation status of R2015K, The gene KCNA2 has a mutation status of G6R, The gene CTTNBP2NL has a mutation status of E171K, The gene S100A13 has a mutation status of M60K, The gene GATAD2B has a mutation status of R249C, The gene IGFN1 has a mutation status of G1209V, The gene ESRRG has a mutation status of S144P, The gene SIPA1L2 has a mutation status of E879K, The gene OR2G2 has a mutation status of V4A, The gene VSIR has a mutation status of E150Ter, The gene ACSM6 has a mutation status of R155D, The gene KAZALD1 has a mutation status of C56R, The gene NR1H3 has a mutation status of A220G, The gene MTCH2 has a mutation status of G11D, The gene MTCH2 has a mutation status of V8M, The gene TRIM49B has a mutation status of E120G, The gene OR4A8 has a mutation status of V78L, The gene FADS1 has a mutation status of L207R, The gene TENM4 has a mutation status of S389I, The gene NAALAD2 has a mutation status of I431T, The gene DYNC2H1 has a mutation status of L1751M, The gene CEP164 has a mutation status of E641V, The gene C2CD2L has a mutation status of A40G, The gene KIRREL3 has a mutation status of L682EfsTer26, The gene GPR162 has a mutation status of S322Y, The gene KMT2D has a mutation status of K3262Ter, The gene ACAD10 has a mutation status of R893C, The gene PDS5B has a mutation status of E395Q, The gene PDS5B has a mutation status of D399H, The gene VPS36 has a mutation status of F217I, The gene GAS6 has a mutation status of E200D, The gene LRFN5 has a mutation status of D258H, The gene TDRD9 has a mutation status of R385Q, The gene SPTBN5 has a mutation status of Q2566Ter, The gene TRIM69 has a mutation status of M284I, The gene NOX5 has a mutation status of K731E, The gene CCDC33 has a mutation status of G603A, The gene IL16 has a mutation status of L309RfsTer13, The gene NPRL3 has a mutation status of R92Ter, The gene OVCA2 has a mutation status of D50G, The gene NLRP1 has a mutation status of V1398D, The gene ABCA6 has a mutation status of T289S, The gene TMC6 has a mutation status of H302P, The gene CDH19 has a mutation status of G556R, The gene MEX3D has a mutation status of D364A, The gene VMAC has a mutation status of L16P, The gene RETN has a mutation status of W81R, The gene RETN has a mutation status of D82G, The gene MYO1F has a mutation status of R878L, The gene GIPC1 has a mutation status of D310Y, The gene CPAMD8 has a mutation status of G430W, The gene CEP89 has a mutation status of E127Q, The gene ZNF345 has a mutation status of H388Q, The gene ZNF585B has a mutation status of C356F, The gene FCGBP has a mutation status of S1228MfsTer5, The gene FCGBP has a mutation status of T1203KfsTer6, The gene CABP5 has a mutation status of E71D, The gene ZNF534 has a mutation status of R625W, The gene LILRA2 has a mutation status of W175S, The gene EPN1 has a mutation status of D402G, The gene TAF1B has a mutation status of S323N, The gene USP34 has a mutation status of F928L, The gene HTRA2 has a mutation status of G353R, The gene CFAP221 has a mutation status of Q247K, The gene LRP1B has a mutation status of S4375G, The gene PTPRN has a mutation status of V347G, The gene SCG2 has a mutation status of F179LfsTer7, The gene SLC24A3 has a mutation status of A10T, The gene TRAPPC10 has a mutation status of H336Y, The gene SNAP29 has a mutation status of G118V, The gene FBXO7 has a mutation status of P327S, The gene PDCD6IP has a mutation status of P841L, The gene CHST13 has a mutation status of R207C, The gene TMCC1 has a mutation status of T159I, The gene TSC22D2 has a mutation status of P529A, The gene FRYL has a mutation status of D1889G, The gene TECRL has a mutation status of T57M, The gene PPEF2 has a mutation status of K254Ter, The gene PTPN13 has a mutation status of S444G, The gene INPP4B has a mutation status of Q464L, The gene ZFR has a mutation status of E621_R627delinsG, The gene NIPBL has a mutation status of S2090G, The gene TNPO1 has a mutation status of P576L, The gene WDR36 has a mutation status of H156P, The gene MCC has a mutation status of S350Ter, The gene PCDHGB3 has a mutation status of A665V, The gene PCDHGC3 has a mutation status of M140del, The gene PCDHGC3 has a mutation status of K141del, The gene LARP1 has a mutation status of Y947F, The gene H2AC11 has a mutation status of R43Q, The gene HLA-DRB1 has a mutation status of S66N, The gene ADGRF5 has a mutation status of W633R, The gene PKHD1 has a mutation status of V881A, The gene IGF2R has a mutation status of L1152P, The gene PLG has a mutation status of R808T, The gene DACT2 has a mutation status of A617G, The gene AMPH has a mutation status of T310N, The gene IKZF1 has a mutation status of S445GfsTer46, The gene IKZF1 has a mutation status of S445delinsWPP, The gene CROT has a mutation status of G502V, The gene AGBL3 has a mutation status of L895I, The gene KIAA1549 has a mutation status of V553M, The gene KLRG2 has a mutation status of K68I, The gene NUDT18 has a mutation status of V204G, The gene NEFM has a mutation status of S46P, The gene CHRNA6 has a mutation status of T315P, The gene DCAF4L2 has a mutation status of V122I, The gene DNAJB5 has a mutation status of Q389Ter, The gene SPATA31D1 has a mutation status of N57Y, The gene ZFP37 has a mutation status of V301A, The gene HSPA5 has a mutation status of K553R, The gene COL5A1 has a mutation status of K1619N, The gene RPA4 has a mutation status of H197D	DLBC
The gene ALDH4A1 has a mutation status of A407T, The gene MROH7 has a mutation status of E1125K, The gene PALMD has a mutation status of E137DfsTer14, The gene SLC22A15 has a mutation status of A66S, The gene GDAP2 has a mutation status of A335P, The gene ASPM has a mutation status of R866G, The gene LMOD1 has a mutation status of A242S, The gene PPP1R12B has a mutation status of G851V, The gene OBSCN has a mutation status of G3054PfsTer4, The gene OR2T1 has a mutation status of L129R, The gene DIP2C has a mutation status of S442G, The gene PTF1A has a mutation status of R241C, The gene ANK3 has a mutation status of T3583M, The gene OR52N4 has a mutation status of Y130S, The gene OR52L1 has a mutation status of V102L, The gene GSTP1 has a mutation status of A152S, The gene ALG8 has a mutation status of T8A, The gene CCDC90B has a mutation status of A164V, The gene KRAS has a mutation status of G12D, The gene MUC19 has a mutation status of R4223_D4252delextTer?, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene HOXC10 has a mutation status of A151V, The gene PPFIA2 has a mutation status of L800S, The gene ACACB has a mutation status of R193L, The gene TTC6 has a mutation status of E252D, The gene SOS2 has a mutation status of S412R, The gene MEIS2 has a mutation status of P56S, The gene SHC4 has a mutation status of A509S, The gene REC114 has a mutation status of V7G, The gene AKAP13 has a mutation status of D1355V, The gene LRRK1 has a mutation status of T715M, The gene N4BP1 has a mutation status of E214VfsTer13, The gene TP53 has a mutation status of I255N, The gene MPRIP has a mutation status of D492Y, The gene NF1 has a mutation status of G1438S, The gene APOH has a mutation status of P81T, The gene SMCHD1 has a mutation status of E1766K, The gene CNDP1 has a mutation status of L315I, The gene CREB3L3 has a mutation status of S200Y, The gene PTPRS has a mutation status of R659Ter, The gene ARHGEF18 has a mutation status of L33M, The gene MUC16 has a mutation status of Q13253E, The gene PLEKHG2 has a mutation status of P484L, The gene FCGBP has a mutation status of A2939P, The gene NLRP4 has a mutation status of G442R, The gene TRMT61B has a mutation status of A35S, The gene ANKRD36 has a mutation status of D317A, The gene RFX8 has a mutation status of D75E, The gene SP5 has a mutation status of P164L, The gene TTN has a mutation status of A28833F, The gene SCYGR2 has a mutation status of H97S, The gene TRPM8 has a mutation status of A102V, The gene RPRD1B has a mutation status of P103R, The gene SRMS has a mutation status of F15del, The gene ADAMTS1 has a mutation status of S384R, The gene EP300 has a mutation status of K1488Ter, The gene TGFBR2 has a mutation status of S156QfsTer4, The gene CCDC13 has a mutation status of I108V, The gene PBRM1 has a mutation status of R549Ter, The gene CD86 has a mutation status of K188E, The gene PPP2R3A has a mutation status of R731K, The gene SLITRK3 has a mutation status of W429LfsTer36, The gene BCHE has a mutation status of N209Y, The gene XXYLT1 has a mutation status of A70S, The gene RCHY1 has a mutation status of A190V, The gene FSTL5 has a mutation status of N46KfsTer21, The gene OSMR has a mutation status of C853G, The gene CDC23 has a mutation status of L179F, The gene PCDHA9 has a mutation status of E40K, The gene GPR151 has a mutation status of G68R, The gene GLI3 has a mutation status of S1028I, The gene PCLO has a mutation status of T2362S, The gene ERVW-1 has a mutation status of L333Ter, The gene DPP6 has a mutation status of T409I, The gene STMN4 has a mutation status of P116S, The gene TRPA1 has a mutation status of Q398R, The gene JPH1 has a mutation status of E85SfsTer70, The gene CCDC171 has a mutation status of S1310F, The gene PRUNE2 has a mutation status of L2591S, The gene TTF1 has a mutation status of D519Y, The gene CAMSAP1 has a mutation status of D1247G, The gene SEC16A has a mutation status of L478FfsTer8, The gene SEC16A has a mutation status of N477S, The gene MT-ND5 has a mutation status of G281S, The gene MT-ND6 has a mutation status of T156I, The gene SLITRK2 has a mutation status of A710S	PAAD
The gene VPS13D has a mutation status of S1800P, The gene SPEN has a mutation status of E1963GfsTer59, The gene SPEN has a mutation status of E1964GfsTer15, The gene INPP5B has a mutation status of K240R, The gene FNBP1L has a mutation status of R580Q, The gene RNPC3 has a mutation status of N342P, The gene FCRL5 has a mutation status of G430E, The gene LAD1 has a mutation status of H34R, The gene MYBPH has a mutation status of A57PfsTer21, The gene USP6NL has a mutation status of K92R, The gene ZNF33B has a mutation status of T602I, The gene MUC5AC has a mutation status of S2302FfsTer68, The gene MUC5AC has a mutation status of T2425R, The gene CALCB has a mutation status of H91del, The gene MYRF has a mutation status of M374K, The gene PITPNM1 has a mutation status of G530S, The gene FAT3 has a mutation status of G4417E, The gene DRD2 has a mutation status of A273S, The gene C2CD2L has a mutation status of D463N, The gene OR10G7 has a mutation status of T8K, The gene ROBO3 has a mutation status of T82M, The gene CD163L1 has a mutation status of E1281K, The gene CD163L1 has a mutation status of W1113L, The gene CLEC1A has a mutation status of C148Ter, The gene PRR4 has a mutation status of N21I, The gene TAS2R43 has a mutation status of L193I, The gene MANSC1 has a mutation status of G333E, The gene LALBA has a mutation status of E68K, The gene LRRIQ1 has a mutation status of E251A, The gene PAH has a mutation status of S359L, The gene TPCN1 has a mutation status of A689D, The gene HSPB8 has a mutation status of S66L, The gene PIWIL1 has a mutation status of E260K, The gene GOLGA3 has a mutation status of Y343C, The gene FRY has a mutation status of G1403E, The gene ATP7B has a mutation status of S177L, The gene CCDC168 has a mutation status of G4299R, The gene CCDC168 has a mutation status of P1001S, The gene ARHGEF40 has a mutation status of S986L, The gene REM2 has a mutation status of P218S, The gene CARMIL3 has a mutation status of S840Y, The gene YLPM1 has a mutation status of P1619S, The gene PPIP5K1 has a mutation status of L1156P, The gene UNC13C has a mutation status of H536R, The gene DENND4A has a mutation status of Y547C, The gene CSPG4 has a mutation status of Q1750K, The gene RPS17 has a mutation status of M105I, The gene TRAP1 has a mutation status of Y559H, The gene UMOD has a mutation status of D166N, The gene SLFN11 has a mutation status of R48L, The gene ARHGAP23 has a mutation status of S463C, The gene KRTAP2-2 has a mutation status of C80_P81delinsWT, The gene DTNA has a mutation status of D26E, The gene WDR7 has a mutation status of L230I, The gene C3 has a mutation status of E689K, The gene DNM2 has a mutation status of A618T, The gene ZNF709 has a mutation status of E635K, The gene ZNF100 has a mutation status of C235G, The gene ZNF99 has a mutation status of E485D, The gene WDR87 has a mutation status of E2791K, The gene PVR has a mutation status of S280R, The gene SIGLEC8 has a mutation status of D405N, The gene PEG3 has a mutation status of S1578P, The gene ZNF17 has a mutation status of F257V, The gene FAM110C has a mutation status of L15F, The gene NRXN1 has a mutation status of H839Y, The gene DGUOK has a mutation status of P246A, The gene SULT1C3 has a mutation status of P95S, The gene ZEB2 has a mutation status of Y1121H, The gene KCNH7 has a mutation status of Q1054Ter, The gene LRP2 has a mutation status of G4301W, The gene SATB2 has a mutation status of R399H, The gene FZD5 has a mutation status of T339N, The gene AHCY has a mutation status of R196W, The gene PHACTR3 has a mutation status of K79N, The gene TMPRSS15 has a mutation status of G907E, The gene SREBF2 has a mutation status of D582N, The gene CHCHD4 has a mutation status of E114Ter, The gene C3orf20 has a mutation status of Y599Ter, The gene FGD5 has a mutation status of F661IfsTer5, The gene FGD5 has a mutation status of F661Ter, The gene SCN10A has a mutation status of T337N, The gene CSNKA2IP has a mutation status of S386L, The gene EPHA3 has a mutation status of V657L, The gene IMPG2 has a mutation status of D436N, The gene AMOTL2 has a mutation status of H177R, The gene DIPK2A has a mutation status of E117Q, The gene ZBBX has a mutation status of V286L, The gene LSG1 has a mutation status of T123A, The gene CLNK has a mutation status of R362C, The gene HS3ST1 has a mutation status of G182D, The gene TLR1 has a mutation status of H111R, The gene N4BP2 has a mutation status of E631V, The gene SDAD1 has a mutation status of P337S, The gene DNAH5 has a mutation status of P3606S, The gene VCAN has a mutation status of P383L, The gene CCNJL has a mutation status of C89Y, The gene WWC1 has a mutation status of E593K, The gene SH3PXD2B has a mutation status of P571A, The gene GRM6 has a mutation status of K528R, The gene SYNGAP1 has a mutation status of G1063D, The gene AARS2 has a mutation status of W210C, The gene OPN5 has a mutation status of G180R, The gene DST has a mutation status of D243N, The gene ABCB5 has a mutation status of S373F, The gene ITPRID1 has a mutation status of E661K, The gene AOAH has a mutation status of R218M, The gene ING3 has a mutation status of T128I, The gene SLC4A2 has a mutation status of A12V, The gene ADAM28 has a mutation status of Q491Ter, The gene SFRP1 has a mutation status of Y127Ter, The gene ZFPM2 has a mutation status of D789N, The gene CPSF1 has a mutation status of A1287T, The gene C8orf33 has a mutation status of S161F, The gene POLR1E has a mutation status of T355A, The gene LAMC3 has a mutation status of Y701F, The gene PRRC2B has a mutation status of N70K, The gene ARRDC1 has a mutation status of R214G, The gene RBMXL3 has a mutation status of H162Q	DLBC
The gene NIPAL3 has a mutation status of T379A, The gene DLGAP3 has a mutation status of Q462E, The gene ZMYM4 has a mutation status of Q859Ter, The gene BEND5 has a mutation status of A73E, The gene BTBD8 has a mutation status of N1558MfsTer20, The gene DCST1 has a mutation status of M537I, The gene SLAMF1 has a mutation status of L185R, The gene CLEC20A has a mutation status of T382I, The gene USH2A has a mutation status of T4347I, The gene TRIM11 has a mutation status of T338P, The gene CYP26C1 has a mutation status of L476P, The gene PLCE1 has a mutation status of D2124E, The gene ALDH18A1 has a mutation status of A152S, The gene CHUK has a mutation status of L7AfsTer32, The gene TACC2 has a mutation status of A788P, The gene NRIP3 has a mutation status of C182S, The gene OR5L1 has a mutation status of I282T, The gene SHANK2 has a mutation status of M182L, The gene CACNA1C has a mutation status of V1406M, The gene NELL2 has a mutation status of T295S, The gene ACVR1B has a mutation status of Q30R, The gene NACA has a mutation status of K1568R, The gene OTOGL has a mutation status of A1322V, The gene C12orf29 has a mutation status of E242G, The gene CCDC38 has a mutation status of Q58K, The gene SLC17A8 has a mutation status of G205W, The gene NT5DC3 has a mutation status of L374_K375delinsFTer, The gene OAS2 has a mutation status of K681Q, The gene MPHOSPH9 has a mutation status of N676S, The gene PCDH17 has a mutation status of D667V, The gene OR4Q3 has a mutation status of F41C, The gene TRAV38-1 has a mutation status of T25S, The gene LRRC9 has a mutation status of S1491L, The gene LRRC9 has a mutation status of N1492K, The gene PTPN21 has a mutation status of D766RfsTer90, The gene AMN has a mutation status of M346L, The gene IGHV4-59 has a mutation status of E35Q, The gene MAP1A has a mutation status of P1833_S1837del, The gene GCNT3 has a mutation status of C70Y, The gene ZNF592 has a mutation status of P44A, The gene AKAP13 has a mutation status of K2635N, The gene DNAH3 has a mutation status of P27Q, The gene ZFHX3 has a mutation status of E3535K, The gene TRPV1 has a mutation status of N192D, The gene ZMYND15 has a mutation status of M684V, The gene TP53 has a mutation status of F134LfsTer14, The gene HS3ST3A1 has a mutation status of K162N, The gene MYO15A has a mutation status of E1406K, The gene FAM210A has a mutation status of L38S, The gene TTC39C has a mutation status of P312L, The gene DSG1 has a mutation status of T930I, The gene SERPINB11 has a mutation status of Q258H, The gene CDH19 has a mutation status of K30N, The gene ATP9B has a mutation status of G61S, The gene REXO1 has a mutation status of D551A, The gene MUC16 has a mutation status of Q13253E, The gene MUC16 has a mutation status of T10751I, The gene KEAP1 has a mutation status of G119_M120delinsV, The gene NCAN has a mutation status of S766R, The gene ZNF585A has a mutation status of N338D, The gene RYR1 has a mutation status of P4386T, The gene PPP5C has a mutation status of R150Q, The gene SHANK1 has a mutation status of P1185Q, The gene LILRA2 has a mutation status of S202A, The gene CAPN14 has a mutation status of K668T, The gene CNRIP1 has a mutation status of P18H, The gene C2CD6 has a mutation status of N1605K, The gene KIAA2012 has a mutation status of Q1040K, The gene SPAG16 has a mutation status of L367Ter, The gene NYAP2 has a mutation status of V344L, The gene SNED1 has a mutation status of P647S, The gene RRBP1 has a mutation status of Q408L, The gene SYNDIG1 has a mutation status of P76S, The gene CDH4 has a mutation status of A394E, The gene KRTAP13-1 has a mutation status of R115S, The gene EMID1 has a mutation status of G229D, The gene FBLN1 has a mutation status of R287C, The gene SETD5 has a mutation status of P169A, The gene HYAL3 has a mutation status of A313G, The gene IL17RD has a mutation status of R535L, The gene ZNF732 has a mutation status of G107Ter, The gene ARAP2 has a mutation status of D1099Y, The gene CRACD has a mutation status of K160R, The gene BMP2K has a mutation status of R656I, The gene THAP9 has a mutation status of W53L, The gene IQCM has a mutation status of F278L, The gene MARCHF1 has a mutation status of P150S, The gene SPOCK3 has a mutation status of T188N, The gene CCDC110 has a mutation status of K590E, The gene SLC12A2 has a mutation status of A103_A107du, The gene AFF4 has a mutation status of A1094T, The gene MZB1 has a mutation status of R80G, The gene LSM11 has a mutation status of P46L, The gene HLA-C has a mutation status of D220A, The gene ZFAND3 has a mutation status of A49V, The gene OOEP has a mutation status of P30T, The gene FIG4 has a mutation status of V328L, The gene TXLNB has a mutation status of A668P, The gene EPM2A has a mutation status of F5L, The gene PCLO has a mutation status of S4837P, The gene COPG2 has a mutation status of I103M, The gene PARP12 has a mutation status of E270K, The gene EPHB6 has a mutation status of A330D, The gene KEL has a mutation status of G4E, The gene CLCN1 has a mutation status of I241V, The gene PTPRN2 has a mutation status of K454Ter, The gene DYNC2I1 has a mutation status of P586T, The gene PRSS55 has a mutation status of P44C, The gene LONRF1 has a mutation status of E755K, The gene LONRF1 has a mutation status of R596Ter, The gene SNTG1 has a mutation status of C403Y, The gene PRDM14 has a mutation status of D180H, The gene TG has a mutation status of A686T, The gene ZC3H3 has a mutation status of L631F, The gene CDK5RAP2 has a mutation status of R144W, The gene MT-CYB has a mutation status of F274L, The gene KRBOX4 has a mutation status of R140W, The gene RAB40A has a mutation status of V189G, The gene AFF2 has a mutation status of R708L, The gene AFF2 has a mutation status of R1238S, The gene RPS4Y2 has a mutation status of T57A	LUAD
The gene PRDM16 has a mutation status of S890Y, The gene DNAJC16 has a mutation status of E394Ter, The gene CLCA2 has a mutation status of S485P, The gene DENND2C has a mutation status of P729T, The gene OR14I1 has a mutation status of C150Ter, The gene HPSE2 has a mutation status of T351I, The gene KNDC1 has a mutation status of P6Q, The gene OR51E1 has a mutation status of V42L, The gene SOX6 has a mutation status of A283S, The gene E2F8 has a mutation status of S533N, The gene PLCB3 has a mutation status of R1137H, The gene C11orf54 has a mutation status of L95I, The gene GRIA4 has a mutation status of S866R, The gene CDON has a mutation status of H1081Q, The gene IGSF9B has a mutation status of S973R, The gene POU6F1 has a mutation status of G363V, The gene SIAH3 has a mutation status of R50Q, The gene OLFM4 has a mutation status of R51M, The gene CARS2 has a mutation status of A481V, The gene VRTN has a mutation status of A251S, The gene PROX2 has a mutation status of E342_Q344del, The gene IGHG3 has a mutation status of Y411Ter, The gene CHRM5 has a mutation status of W525Ter, The gene EIF2AK4 has a mutation status of T791K, The gene GNB5 has a mutation status of K189Q, The gene SCAMP2 has a mutation status of G246V, The gene MMP25 has a mutation status of R438L, The gene CREBBP has a mutation status of G221V, The gene EARS2 has a mutation status of D281G, The gene PKD1L2 has a mutation status of A17D, The gene HS3ST3A1 has a mutation status of G51E, The gene SLFN12L has a mutation status of K102N, The gene FBF1 has a mutation status of A919G, The gene CYGB has a mutation status of S188L, The gene MYOM1 has a mutation status of V413M, The gene MAMSTR has a mutation status of R113M, The gene KCNA7 has a mutation status of A275V, The gene LILRB1 has a mutation status of Y99I, The gene NLRP5 has a mutation status of K1090N, The gene DUXA has a mutation status of P177L, The gene SOS1 has a mutation status of N233Y, The gene MOB1A has a mutation status of A44SfsTer6, The gene POLR1B has a mutation status of Y607F, The gene ZRANB3 has a mutation status of H513R, The gene XIRP2 has a mutation status of E721K, The gene ASXL1 has a mutation status of Y591Ter, The gene ADAMTS1 has a mutation status of V825F, The gene RUNX1 has a mutation status of T148MfsTer6, The gene PDXK has a mutation status of Q288P, The gene INPP5J has a mutation status of N539K, The gene PACSIN2 has a mutation status of E227D, The gene SRGAP3 has a mutation status of T983K, The gene IL1RAP has a mutation status of E453A, The gene CCKAR has a mutation status of V311A, The gene ADGRL3 has a mutation status of T1236I, The gene UGT2A1 has a mutation status of Y221H, The gene TET2 has a mutation status of S825Ter, The gene PCDHB6 has a mutation status of P104L, The gene RIPK1 has a mutation status of A569V, The gene ZKSCAN3 has a mutation status of W463Ter, The gene DDR1 has a mutation status of S360R, The gene HCG22 has a mutation status of D185E, The gene CCHCR1 has a mutation status of L394F, The gene PEX7 has a mutation status of L238F, The gene IKZF1 has a mutation status of D186Y, The gene AUTS2 has a mutation status of S612Y, The gene DYNC1I1 has a mutation status of F262L, The gene MUC3A has a mutation status of T289M, The gene LRRC17 has a mutation status of T173M, The gene EZH2 has a mutation status of R690H, The gene EN2 has a mutation status of R65G, The gene PMP2 has a mutation status of L6Q, The gene ESRP1 has a mutation status of Y176D, The gene MTDH has a mutation status of E277A, The gene FOCAD has a mutation status of K37N, The gene FRMPD1 has a mutation status of H1386Y, The gene NFIL3 has a mutation status of R91C, The gene SLC25A6 has a mutation status of P28S, The gene SMC1A has a mutation status of G707E	LAML
The gene PADI4 has a mutation status of K244R, The gene CSMD2 has a mutation status of I3564V, The gene KIAA0319L has a mutation status of Q293PfsTer31, The gene LRRC7 has a mutation status of R43W, The gene ERICH3 has a mutation status of S1009L, The gene H2AC20 has a mutation status of L24R, The gene LCE2C has a mutation status of S72F, The gene C1orf68 has a mutation status of G220R, The gene CASQ1 has a mutation status of E233V, The gene TASOR2 has a mutation status of F2197L, The gene CUL2 has a mutation status of S481N, The gene CEP55 has a mutation status of D247E, The gene DENND5A has a mutation status of I952V, The gene PLCB3 has a mutation status of S292A, The gene HEPHL1 has a mutation status of Y416D, The gene ARHGAP32 has a mutation status of A278V, The gene VWF has a mutation status of A2414T, The gene ACRBP has a mutation status of R273G, The gene LRRK2 has a mutation status of Y636H, The gene SLC4A8 has a mutation status of V286A, The gene PXN has a mutation status of V687L, The gene ZNF219 has a mutation status of P109_E110insA, The gene PAX9 has a mutation status of Q257H, The gene FCF1 has a mutation status of Q22R, The gene IFT140 has a mutation status of V569A, The gene CLN3 has a mutation status of Y124C, The gene TAOK2 has a mutation status of P355L, The gene ZNF668 has a mutation status of H358N, The gene NLRC5 has a mutation status of L607F, The gene TRPV1 has a mutation status of D625G, The gene TP53 has a mutation status of Y205H, The gene MYH1 has a mutation status of R1438S, The gene EFCAB5 has a mutation status of Q38H, The gene CDH7 has a mutation status of L242R, The gene MUC16 has a mutation status of P5040S, The gene ICAM5 has a mutation status of L21V, The gene ZNF433 has a mutation status of V9M, The gene ADGRE5 has a mutation status of G634V, The gene GMIP has a mutation status of P779L, The gene CEP89 has a mutation status of G349V, The gene FCGBP has a mutation status of G1230_P1231del, The gene FCGBP has a mutation status of T1203KfsTer6, The gene FCGBP has a mutation status of A1165GfsTer13, The gene FCGBP has a mutation status of E1160GfsTer144, The gene SHKBP1 has a mutation status of P698L, The gene ITPKC has a mutation status of F568V, The gene KPTN has a mutation status of D289Y, The gene LILRB1 has a mutation status of Q401L, The gene ZNF444 has a mutation status of R289S, The gene PCGF1 has a mutation status of E167K, The gene TTN has a mutation status of L34665V, The gene ITGAV has a mutation status of V806HfsTer3, The gene CHPF has a mutation status of E700M, The gene TPTE has a mutation status of R261G, The gene TRIOBP has a mutation status of L1819V, The gene CACNA1I has a mutation status of S569R, The gene VHL has a mutation status of R200W, The gene SCN5A has a mutation status of L56M, The gene TMEM45A has a mutation status of Y139C, The gene NXPE3 has a mutation status of L23P, The gene MYH15 has a mutation status of C1332Y, The gene PLCXD2 has a mutation status of L106P, The gene NEK11 has a mutation status of S574P, The gene MUC4 has a mutation status of L3542T, The gene MUC4 has a mutation status of S3541D, The gene DGKQ has a mutation status of S634P, The gene CTBP1 has a mutation status of R162G, The gene PAICS has a mutation status of D221N, The gene ENPEP has a mutation status of W408C, The gene BLTP1 has a mutation status of L3810F, The gene GLRB has a mutation status of S93P, The gene CTNND2 has a mutation status of L307V, The gene PDZD2 has a mutation status of I637V, The gene GPBP1 has a mutation status of D136V, The gene MCC has a mutation status of N283S, The gene SLC22A5 has a mutation status of I89V, The gene PCDHB12 has a mutation status of R478_D479del, The gene FGF18 has a mutation status of H205R, The gene HLA-A has a mutation status of G314V, The gene HLA-DRB5 has a mutation status of G8E, The gene NCR2 has a mutation status of S59L, The gene CASP8AP2 has a mutation status of K1536Q, The gene RSPH4A has a mutation status of I471T, The gene SYNE1 has a mutation status of G7350R, The gene EGFR has a mutation status of L747_E749del, The gene EGFR has a mutation status of A750P, The gene MUC3A has a mutation status of T303V, The gene MKRN1 has a mutation status of A26S, The gene RBM33 has a mutation status of P615_H635del, The gene FABP4 has a mutation status of D48Y, The gene LHX3 has a mutation status of S343R, The gene SHOX has a mutation status of A214D, The gene SHROOM2 has a mutation status of D613A, The gene RTL3 has a mutation status of L268Q, The gene SYTL4 has a mutation status of P144R, The gene GUCY2F has a mutation status of P1069L	LUAD
The gene ENO1 has a mutation status of T229N, The gene PEX14 has a mutation status of R350H, The gene MTOR has a mutation status of E1799K, The gene FAM43B has a mutation status of N7S, The gene ADPRS has a mutation status of A2S, The gene MAST2 has a mutation status of T666S, The gene ASB17 has a mutation status of D252E, The gene RPAP2 has a mutation status of I329L, The gene FMOD has a mutation status of Y319_G322del, The gene ZBED6 has a mutation status of S14Y, The gene MRC1 has a mutation status of S288R, The gene ARHGAP22 has a mutation status of A139T, The gene ARHGAP22 has a mutation status of V137E, The gene HECTD2 has a mutation status of A18V, The gene SLIT1 has a mutation status of C940LfsTer7, The gene SLIT1 has a mutation status of P708S, The gene CALHM1 has a mutation status of S142N, The gene SLC22A18 has a mutation status of I202T, The gene STIM1 has a mutation status of V280F, The gene PRDM11 has a mutation status of Q1096L, The gene PRPF19 has a mutation status of T268N, The gene CD6 has a mutation status of L27I, The gene CD6 has a mutation status of D191H, The gene DAGLA has a mutation status of E342K, The gene PAAF1 has a mutation status of S327F, The gene FAT3 has a mutation status of K1948R, The gene MMP10 has a mutation status of E84Ter, The gene ST14 has a mutation status of A240S, The gene IQSEC3 has a mutation status of R631C, The gene ITFG2 has a mutation status of M178L, The gene MUC19 has a mutation status of T3551A, The gene C12orf54 has a mutation status of R30K, The gene CUX2 has a mutation status of R701S, The gene VSIG10 has a mutation status of P311L, The gene FREM2 has a mutation status of F127L, The gene DCAF11 has a mutation status of R408W, The gene PRORP has a mutation status of S476L, The gene ERO1A has a mutation status of L17M, The gene DACT1 has a mutation status of P17L, The gene CCDC196 has a mutation status of K27RfsTer3, The gene LTBP2 has a mutation status of G729V, The gene FCF1 has a mutation status of R188Q, The gene DMXL2 has a mutation status of Q2650H, The gene GCNT3 has a mutation status of R388Q, The gene MESP1 has a mutation status of S237I, The gene CACNA1H has a mutation status of R762W, The gene PGP has a mutation status of G214C, The gene ARHGAP17 has a mutation status of N828T, The gene WDR81 has a mutation status of L575M, The gene TP53 has a mutation status of R248Q, The gene TOP2A has a mutation status of T930I, The gene WFIKKN2 has a mutation status of R541L, The gene CACNG1 has a mutation status of T12I, The gene LRRC30 has a mutation status of D65N, The gene BSG has a mutation status of G303D, The gene ZNF562 has a mutation status of M28I, The gene ARHGAP33 has a mutation status of Q553K, The gene ZNF382 has a mutation status of I128V, The gene LRFN1 has a mutation status of A126E, The gene NUMBL has a mutation status of A25S, The gene FKRP has a mutation status of E285Ter, The gene TRPM4 has a mutation status of R770C, The gene CFAP36 has a mutation status of V263A, The gene MEIS1 has a mutation status of I19T, The gene CDH22 has a mutation status of E741D, The gene DSCAM has a mutation status of E1274K, The gene IL17RA has a mutation status of N67D, The gene TRMT2A has a mutation status of L214I, The gene SHANK3 has a mutation status of A1204D, The gene DLEC1 has a mutation status of L71M, The gene CCDC12 has a mutation status of E101D, The gene RASSF1 has a mutation status of C102F, The gene ERC2 has a mutation status of S448L, The gene ZBTB20 has a mutation status of G257D, The gene DGKG has a mutation status of E672Ter, The gene LAP3 has a mutation status of P5H, The gene UGT2B15 has a mutation status of G100D, The gene RCHY1 has a mutation status of K58E, The gene PGRMC2 has a mutation status of T157R, The gene POU4F2 has a mutation status of L286SfsTer27, The gene LRRC14B has a mutation status of A110D, The gene AP3B1 has a mutation status of Q363R, The gene SLC12A2 has a mutation status of D1066N, The gene PCDHGB3 has a mutation status of G218S, The gene GABRA1 has a mutation status of T333R, The gene SPDL1 has a mutation status of R453S, The gene NPM1 has a mutation status of N38D, The gene LMAN2 has a mutation status of R223H, The gene TBC1D9B has a mutation status of H63Q, The gene SLC22A23 has a mutation status of S116Ter, The gene SOX4 has a mutation status of G183A, The gene HLA-DQB1 has a mutation status of P84E, The gene HLA-DQA2 has a mutation status of A16T, The gene RUNX2 has a mutation status of A525S, The gene ABCA13 has a mutation status of H1648R, The gene EGFR has a mutation status of A289D, The gene VPS50 has a mutation status of D46Ter, The gene PAX4 has a mutation status of A298T, The gene C8orf74 has a mutation status of A202D, The gene NPBWR1 has a mutation status of A114D, The gene DENND3 has a mutation status of A2E, The gene EPPK1 has a mutation status of A2155P, The gene TMEM8B has a mutation status of A625E, The gene FOXB2 has a mutation status of A414D, The gene SLC28A3 has a mutation status of P409S, The gene TRIM14 has a mutation status of A331V, The gene TRIM14 has a mutation status of Q329K, The gene FCN2 has a mutation status of K304Ter, The gene ARAF has a mutation status of I232M, The gene IQSEC2 has a mutation status of V786L, The gene DACH2 has a mutation status of A11E, The gene BTK has a mutation status of C464F	GBMLGG
The gene PRDM16 has a mutation status of D630G, The gene TAS1R1 has a mutation status of T198I, The gene SYTL1 has a mutation status of A214T, The gene SRSF4 has a mutation status of R139C, The gene DNAI4 has a mutation status of K794R, The gene C1orf141 has a mutation status of D10N, The gene CELSR2 has a mutation status of R2015K, The gene STRIP1 has a mutation status of E811G, The gene WDR3 has a mutation status of R706K, The gene NAV1 has a mutation status of A349H, The gene TAF5L has a mutation status of R535H, The gene RYR2 has a mutation status of H1710N, The gene FMN2 has a mutation status of A160V, The gene ZNF672 has a mutation status of R128G, The gene KIF20B has a mutation status of E590D, The gene NUP98 has a mutation status of T459FfsTer31, The gene PATL1 has a mutation status of V500F, The gene UNC93B1 has a mutation status of P575Q, The gene NUMA1 has a mutation status of A1342V, The gene TECTA has a mutation status of D250Y, The gene KIRREL3 has a mutation status of P650L, The gene SLC6A13 has a mutation status of T596K, The gene MEDAG has a mutation status of S157F, The gene RFXAP has a mutation status of E228Ter, The gene SSTR1 has a mutation status of R197H, The gene OTX2 has a mutation status of Q295Ter, The gene PCNX1 has a mutation status of R1001C, The gene TMEM121 has a mutation status of K142E, The gene IGHV4-61 has a mutation status of S52D, The gene STRA6 has a mutation status of A300VfsTer3, The gene PKD1 has a mutation status of L3901V, The gene PAQR4 has a mutation status of A91T, The gene GPRC5B has a mutation status of I57F, The gene RRAD has a mutation status of P28T, The gene MTSS2 has a mutation status of L168M, The gene PABPN1L has a mutation status of D233TfsTer53, The gene ABR has a mutation status of N755S, The gene PLSCR3 has a mutation status of E107Ter, The gene TP53 has a mutation status of Q317Ter, The gene TP53 has a mutation status of G245D, The gene CTC1 has a mutation status of C82F, The gene ZSWIM7 has a mutation status of L95Q, The gene IKZF3 has a mutation status of L162R, The gene NFE2L1 has a mutation status of L413V, The gene EVPL has a mutation status of L156V, The gene NOTUM has a mutation status of G61A, The gene TXNDC2 has a mutation status of P353S, The gene ARID3A has a mutation status of D30PfsTer95, The gene CBARP has a mutation status of I181M, The gene TCF3 has a mutation status of E501D, The gene ARHGEF18 has a mutation status of S485G, The gene MUC16 has a mutation status of S8972P, The gene ZNF441 has a mutation status of A372G, The gene MEF2B has a mutation status of N49S, The gene ZNF208 has a mutation status of G1203V, The gene ZNF257 has a mutation status of C126H, The gene ZNF729 has a mutation status of C908S, The gene RYR1 has a mutation status of A4739V, The gene MED29 has a mutation status of G16du, The gene HIF3A has a mutation status of D546E, The gene KIR2DL1 has a mutation status of D184N, The gene KIR3DL1 has a mutation status of A371S, The gene BIN1 has a mutation status of G320D, The gene FSIP2 has a mutation status of I3880M, The gene NCAM2 has a mutation status of I489T, The gene HDHD5 has a mutation status of N323S, The gene NF2 has a mutation status of Y207Ter, The gene TRABD has a mutation status of R111C, The gene ARPP21 has a mutation status of P647S, The gene SCN5A has a mutation status of R121Q, The gene KLHL40 has a mutation status of F117L, The gene COL7A1 has a mutation status of F1026del, The gene DNAH1 has a mutation status of K1844N, The gene PHLDB2 has a mutation status of I597V, The gene TEX55 has a mutation status of V463A, The gene CFAP92 has a mutation status of M906L, The gene PLSCR4 has a mutation status of P6H, The gene C3orf33 has a mutation status of L83Ter, The gene HRG has a mutation status of G296E, The gene MUC4 has a mutation status of D3957S, The gene MUC4 has a mutation status of P3312S, The gene POLN has a mutation status of N382S, The gene KIAA0232 has a mutation status of V574A, The gene DNAJB14 has a mutation status of N365S, The gene NPY2R has a mutation status of T13R, The gene HPF1 has a mutation status of S135Y, The gene MARCHF6 has a mutation status of R113C, The gene OTULIN has a mutation status of R30L, The gene CDH10 has a mutation status of G244S, The gene OXCT1 has a mutation status of S33T, The gene YTHDC2 has a mutation status of F568V, The gene GRXCR2 has a mutation status of C235F, The gene NMUR2 has a mutation status of F215L, The gene FAM8A1 has a mutation status of L338I, The gene MDFI has a mutation status of A230T, The gene TDRD6 has a mutation status of A1619P, The gene MFSD4B has a mutation status of L182Y, The gene SDK1 has a mutation status of E2134du, The gene PCLO has a mutation status of T3186K, The gene MUC3A has a mutation status of W18G, The gene PLXNA4 has a mutation status of M1017I, The gene SPIDR has a mutation status of S64L, The gene PRKDC has a mutation status of K3873R, The gene NOTCH1 has a mutation status of H2428PfsTer7, The gene MT-ND5 has a mutation status of T533M, The gene ZMAT1 has a mutation status of E679Ter	DLBC
The gene SLC30A2 has a mutation status of A302V, The gene PRRC2C has a mutation status of P2085H, The gene OR14A2 has a mutation status of Y121C, The gene ZNF248 has a mutation status of Y520C, The gene MKI67 has a mutation status of Q2202H, The gene MKI67 has a mutation status of E998K, The gene SLC35C1 has a mutation status of R229S, The gene RAD51AP1 has a mutation status of K260R, The gene MYF5 has a mutation status of S216F, The gene CCDC63 has a mutation status of Y256H, The gene TNFRSF19 has a mutation status of S24L, The gene DACH1 has a mutation status of S82_G121del, The gene AJUBA has a mutation status of R218W, The gene SAV1 has a mutation status of H40R, The gene SLC8A3 has a mutation status of I114LfsTer23, The gene PLCB2 has a mutation status of V855I, The gene SNX22 has a mutation status of W119Ter, The gene LOXL1 has a mutation status of Y52C, The gene TBL3 has a mutation status of Q710H, The gene AMDHD2 has a mutation status of G300S, The gene GP2 has a mutation status of H125Y, The gene SEZ6L2 has a mutation status of I353T, The gene KIFC3 has a mutation status of A12D, The gene USP22 has a mutation status of G108R, The gene RUNDC1 has a mutation status of A3V, The gene C19orf25 has a mutation status of A30V, The gene C19orf25 has a mutation status of E25Ter, The gene ZNF66 has a mutation status of H537Y, The gene NPHS1 has a mutation status of N436S, The gene ACP7 has a mutation status of A74T, The gene DACT3 has a mutation status of P531S, The gene KIAA1755 has a mutation status of L450V, The gene SLC9A8 has a mutation status of V454I, The gene APOL5 has a mutation status of E224G, The gene PRKCD has a mutation status of N193Y, The gene KDR has a mutation status of H381Y, The gene DDX41 has a mutation status of T236R, The gene ADAMTS2 has a mutation status of A35T, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB1 has a mutation status of P84E, The gene KLHL31 has a mutation status of D24V, The gene AHCYL2 has a mutation status of G48V, The gene TMEM209 has a mutation status of G366V, The gene CSMD3 has a mutation status of G187S, The gene TONSL has a mutation status of R1076C, The gene MFSD3 has a mutation status of A43V, The gene PUM3 has a mutation status of P552A, The gene UNC13B has a mutation status of A3188P, The gene NACC2 has a mutation status of L187P, The gene IQSEC2 has a mutation status of P1369T, The gene PHF8 has a mutation status of F455S, The gene CLIC2 has a mutation status of I192V	DLBC
The gene CASZ1 has a mutation status of R690H, The gene PDIK1L has a mutation status of E281K, The gene TSSK3 has a mutation status of M76T, The gene PHC2 has a mutation status of R698L, The gene CLCA1 has a mutation status of T574N, The gene NRAS has a mutation status of G12D, The gene SPRR2B has a mutation status of P65R, The gene ASPM has a mutation status of Q1613Ter, The gene PLXNA2 has a mutation status of R1705L, The gene H3-3A has a mutation status of K28M, The gene GREM2 has a mutation status of M158K, The gene ITIH5 has a mutation status of A154T, The gene CYP17A1 has a mutation status of D281N, The gene NT5C2 has a mutation status of R238W, The gene KCNK18 has a mutation status of A156E, The gene FANK1 has a mutation status of D138V, The gene FAM234B has a mutation status of E479KfsTer34, The gene KMT2D has a mutation status of S543Ter, The gene CBX5 has a mutation status of T188K, The gene ZNF385A has a mutation status of A333T, The gene TXNRD1 has a mutation status of G451D, The gene ZNF84 has a mutation status of K737N, The gene ADPRHL1 has a mutation status of A1912D, The gene ZNF219 has a mutation status of G401V, The gene PRKD1 has a mutation status of R8W, The gene LACTB has a mutation status of A107D, The gene CHD2 has a mutation status of E412T, The gene PGP has a mutation status of S95I, The gene TGFB1I1 has a mutation status of E250K, The gene ZNF469 has a mutation status of H2569N, The gene ANKRD11 has a mutation status of G2273A, The gene KDM6B has a mutation status of P1056L, The gene GOSR1 has a mutation status of G94D, The gene KRT10 has a mutation status of S275R, The gene CACNA1G has a mutation status of D2286E, The gene DNAH17 has a mutation status of R3374Q, The gene KCTD1 has a mutation status of K393Ter, The gene GAREM1 has a mutation status of A522V, The gene MYO5B has a mutation status of E1755K, The gene SF3A2 has a mutation status of L247M, The gene NDUFA13 has a mutation status of V101L, The gene TGFB1 has a mutation status of S209R, The gene POLD1 has a mutation status of I337N, The gene RFPL4A has a mutation status of Q95K, The gene ATAD2B has a mutation status of Q896E, The gene PRKCE has a mutation status of V160A, The gene DCTN1 has a mutation status of V60M, The gene RANBP2 has a mutation status of Q1054_P1055delinsHS, The gene CSRNP3 has a mutation status of F317L, The gene ITGA4 has a mutation status of I400S, The gene FSIP2 has a mutation status of L1991F, The gene DNAH7 has a mutation status of T2224K, The gene PIGT has a mutation status of F496I, The gene CRKL has a mutation status of P215del, The gene PISD has a mutation status of P42H, The gene SETD5 has a mutation status of C109S, The gene NEK10 has a mutation status of D769V, The gene CLASP2 has a mutation status of G1103R, The gene FLNB has a mutation status of M1?, The gene TRIM42 has a mutation status of A136T, The gene GBA3 has a mutation status of D23N, The gene REST has a mutation status of R1067S, The gene TMPRSS11B has a mutation status of P373T, The gene FRAS1 has a mutation status of E2212V, The gene ADH1A has a mutation status of S118T, The gene FAT1 has a mutation status of G2925E, The gene DNAH5 has a mutation status of A2298T, The gene PDE4D has a mutation status of D200E, The gene MAN2A1 has a mutation status of D355H, The gene PCDHGB2 has a mutation status of Y418C, The gene DOCK2 has a mutation status of R214Q, The gene HLA-A has a mutation status of I121R, The gene HLA-A has a mutation status of K292E, The gene SAYSD1 has a mutation status of P56S, The gene TTBK1 has a mutation status of E402D, The gene MAP3K5 has a mutation status of A369V, The gene RPS6KA2 has a mutation status of A632S, The gene SNX13 has a mutation status of S713N, The gene GLI3 has a mutation status of S1028I, The gene MTERF1 has a mutation status of F44L, The gene SH2B2 has a mutation status of G308S, The gene RELN has a mutation status of N2624I, The gene FAM131B has a mutation status of I114KfsTer43, The gene ZNF783 has a mutation status of G522S, The gene TNKS has a mutation status of D296E, The gene OPRK1 has a mutation status of P367T, The gene ZFHX4 has a mutation status of S1166LfsTer8, The gene EPPK1 has a mutation status of T1986R, The gene COL5A1 has a mutation status of L1415F, The gene ABCA2 has a mutation status of E120V, The gene TEX13C has a mutation status of P299T	DLBC
The gene TTLL10 has a mutation status of G234Ter, The gene FNDC10 has a mutation status of W93C, The gene SLC35E2B has a mutation status of G208C, The gene TMEM52 has a mutation status of L201I, The gene SPEN has a mutation status of P3245T, The gene KLHDC7A has a mutation status of A442PfsTer9, The gene TAS1R2 has a mutation status of R317A, The gene SYF2 has a mutation status of G17W, The gene SYF2 has a mutation status of A14S, The gene MACF1 has a mutation status of V1975L, The gene HIVEP3 has a mutation status of P2134Q, The gene L1TD1 has a mutation status of D34A, The gene FPGT has a mutation status of M150V, The gene RTCA has a mutation status of Q177TfsTer9, The gene PTGFRN has a mutation status of H201N, The gene ADAM30 has a mutation status of G319E, The gene SCAMP3 has a mutation status of R47Q, The gene PRRC2C has a mutation status of N176K, The gene GPR25 has a mutation status of R317L, The gene LGR6 has a mutation status of E155Ter, The gene RABIF has a mutation status of R29P, The gene SLC45A3 has a mutation status of G449E, The gene FCMR has a mutation status of K361N, The gene CR1 has a mutation status of C266S, The gene WDR26 has a mutation status of P87H, The gene DNAH14 has a mutation status of R1865del, The gene OBSCN has a mutation status of R225L, The gene OBSCN has a mutation status of P2906R, The gene KIF26B has a mutation status of P284Q, The gene TRIM58 has a mutation status of W116G, The gene TRIM58 has a mutation status of V117G, The gene DIP2C has a mutation status of P12S, The gene ADARB2 has a mutation status of P208T, The gene PFKFB3 has a mutation status of F87L, The gene PLXDC2 has a mutation status of L329I, The gene EBLN1 has a mutation status of K267N, The gene GJD4 has a mutation status of P335T, The gene GJD4 has a mutation status of R337S, The gene KIFBP has a mutation status of I506K, The gene SRGN has a mutation status of S46F, The gene SPOCK2 has a mutation status of T85P, The gene LDB3 has a mutation status of T427I, The gene LZTS2 has a mutation status of P315Q, The gene PSD has a mutation status of E59G, The gene NT5C2 has a mutation status of L347F, The gene PNLIPRP2 has a mutation status of W125Ter, The gene KNDC1 has a mutation status of D493Y, The gene SCART1 has a mutation status of G177C, The gene TIMM10B has a mutation status of R3L, The gene CHST1 has a mutation status of C34AfsTer84, The gene CELF1 has a mutation status of P279Q, The gene RAB3IL1 has a mutation status of Q58K, The gene TM7SF2 has a mutation status of G102C, The gene LRP5 has a mutation status of P8Q, The gene MYO7A has a mutation status of P1725Q, The gene MAML2 has a mutation status of G19W, The gene CEP126 has a mutation status of S367L, The gene DYNC2H1 has a mutation status of K2127E, The gene CACNA2D4 has a mutation status of D885V, The gene PHC1 has a mutation status of G289C, The gene SLCO1A2 has a mutation status of G254E, The gene RAPGEF3 has a mutation status of E788Ter, The gene RAPGEF3 has a mutation status of F428L, The gene KMT2D has a mutation status of G2501W, The gene FIGNL2 has a mutation status of G94W, The gene KRT83 has a mutation status of C476Ter, The gene RASSF9 has a mutation status of T196S, The gene TMEM132C has a mutation status of D1042G, The gene COL4A1 has a mutation status of L1447P, The gene REM2 has a mutation status of T309N, The gene ZFHX2 has a mutation status of T946I, The gene JPH4 has a mutation status of Q132Ter, The gene LTB4R2 has a mutation status of A80D, The gene TTC6 has a mutation status of R996S, The gene KLHDC1 has a mutation status of G29V, The gene RTN1 has a mutation status of P538T, The gene HIF1A has a mutation status of G726D, The gene PAPLN has a mutation status of S78R, The gene IFT43 has a mutation status of G150W, The gene VASH1 has a mutation status of P25H, The gene NRXN3 has a mutation status of T1401A, The gene GPR65 has a mutation status of C283Y, The gene EML5 has a mutation status of G967R, The gene TTC8 has a mutation status of G133A, The gene PPP4R3A has a mutation status of P699L, The gene DYNC1H1 has a mutation status of D4257G, The gene TNFAIP2 has a mutation status of P240T, The gene FMN1 has a mutation status of H200Y, The gene EIF2AK4 has a mutation status of P940S, The gene CCPG1 has a mutation status of Q638Ter, The gene SNX22 has a mutation status of P11H, The gene RPL4 has a mutation status of G382R, The gene ISLR2 has a mutation status of V580G, The gene RASGRF1 has a mutation status of M1239I, The gene MEX3B has a mutation status of G413W, The gene ADAMTSL3 has a mutation status of D368Y, The gene ARHGDIG has a mutation status of G33W, The gene TELO2 has a mutation status of Q634K, The gene DPEP3 has a mutation status of P67Q, The gene CPHXL has a mutation status of L108F, The gene FOXC2 has a mutation status of A312S, The gene ZCCHC14 has a mutation status of G971C, The gene ZFPM1 has a mutation status of P117Q, The gene RAP1GAP2 has a mutation status of P681Q, The gene NCBP3 has a mutation status of G35C, The gene SPNS2 has a mutation status of P337Q, The gene TP53 has a mutation status of H233del, The gene LLGL1 has a mutation status of S227Ter, The gene SLC47A1 has a mutation status of S23Ter, The gene RAB11FIP4 has a mutation status of Q50H, The gene C17orf113 has a mutation status of R178M, The gene PLCD3 has a mutation status of R70L, The gene TANC2 has a mutation status of Q1136K, The gene CEP112 has a mutation status of E288D, The gene MYO15B has a mutation status of S813Y, The gene EXOC7 has a mutation status of E21Ter, The gene RPTOR has a mutation status of F263S, The gene SS18 has a mutation status of Q81Ter, The gene DSC2 has a mutation status of K121N, The gene EPG5 has a mutation status of S16R, The gene TSHZ1 has a mutation status of S176H, The gene DOT1L has a mutation status of K1228N, The gene HMG20B has a mutation status of K58N, The gene MUC16 has a mutation status of S2595R, The gene MUC16 has a mutation status of E388D, The gene ZNF560 has a mutation status of Q246L, The gene OR10H4 has a mutation status of I8M, The gene CALR3 has a mutation status of L276V, The gene ELL has a mutation status of Q552H, The gene FFAR1 has a mutation status of H86N, The gene THAP8 has a mutation status of P123Q, The gene SUPT5H has a mutation status of P172T, The gene SELENOV has a mutation status of W92L, The gene PSG3 has a mutation status of C9Y, The gene PSG9 has a mutation status of P416L, The gene CYTH2 has a mutation status of H255D, The gene SCAF1 has a mutation status of P507T, The gene ZNF765 has a mutation status of S189Y, The gene ZNF444 has a mutation status of P325H, The gene ZNF71 has a mutation status of A198V, The gene SMIM17 has a mutation status of W29L, The gene RAD51AP2 has a mutation status of P119S, The gene PRR30 has a mutation status of T353I, The gene ARHGEF33 has a mutation status of F825L, The gene DYSF has a mutation status of S680Ter, The gene VAMP8 has a mutation status of Q29K, The gene LONRF2 has a mutation status of Q25_R26delinsHS, The gene CKAP2L has a mutation status of E641D, The gene TTN has a mutation status of A18470V, The gene TTN has a mutation status of M10484V, The gene GLS has a mutation status of A537E, The gene UNC80 has a mutation status of L3030M, The gene ABCA12 has a mutation status of K2017T, The gene ZNF142 has a mutation status of P1212S, The gene CNPPD1 has a mutation status of H337P, The gene OBSL1 has a mutation status of P860S, The gene COL4A3 has a mutation status of G49W, The gene LZTS3 has a mutation status of T522P, The gene HSPA12B has a mutation status of R295S, The gene SHLD1 has a mutation status of S40R, The gene CST8 has a mutation status of K26N, The gene ASXL1 has a mutation status of G646WfsTer12, The gene RIPOR3 has a mutation status of K213R, The gene GNAS has a mutation status of K223N, The gene LAMA5 has a mutation status of G3129V, The gene LAMA5 has a mutation status of G704W, The gene HELZ2 has a mutation status of L2371V, The gene DSCAM has a mutation status of Q1623H, The gene TSPEAR has a mutation status of R662M, The gene MN1 has a mutation status of P594Q, The gene MN1 has a mutation status of H591Q, The gene TTC28 has a mutation status of S1963Y, The gene GAS2L1 has a mutation status of P383H, The gene CCDC157 has a mutation status of Q457K, The gene SEC14L3 has a mutation status of V274G, The gene CBX6 has a mutation status of G403V, The gene CELSR1 has a mutation status of P624H, The gene CELSR1 has a mutation status of A186D, The gene SEC13 has a mutation status of T133I, The gene PPARG has a mutation status of S156KfsTer2, The gene ITGA9 has a mutation status of P764Q, The gene ULK4 has a mutation status of K216E, The gene PDZRN3 has a mutation status of G88C, The gene GSK3B has a mutation status of V126I, The gene UBA5 has a mutation status of R37W, The gene MFSD10 has a mutation status of G334W, The gene BMP2K has a mutation status of E1148K, The gene PITX2 has a mutation status of D48Y, The gene VEGFC has a mutation status of H92Y, The gene TENM3 has a mutation status of F2690L, The gene ICE1 has a mutation status of E5Ter, The gene ARSK has a mutation status of H236R, The gene MEGF10 has a mutation status of C587Y, The gene PITX1 has a mutation status of P67T, The gene PCDHGA1 has a mutation status of R747W, The gene GEMIN5 has a mutation status of P53T, The gene ATXN1 has a mutation status of Q204_Q205insKQ, The gene ZNF391 has a mutation status of K222N, The gene HLA-C has a mutation status of S140L, The gene BRD2 has a mutation status of N429S, The gene CPNE5 has a mutation status of E66K, The gene KLHL31 has a mutation status of A541E, The gene PHACTR2 has a mutation status of R63H, The gene ZC2HC1B has a mutation status of R147Q, The gene PRR18 has a mutation status of G284W, The gene WDR27 has a mutation status of N718K, The gene DLL1 has a mutation status of R484M, The gene UNCX has a mutation status of K375N, The gene AUTS2 has a mutation status of P1054T, The gene MAGI2 has a mutation status of K1441M, The gene NYAP1 has a mutation status of V44G, The gene SMKR1 has a mutation status of M32I, The gene OR2A12 has a mutation status of C96S, The gene NOM1 has a mutation status of R28G, The gene NOM1 has a mutation status of P30A, The gene UBE3C has a mutation status of K868N, The gene CSMD1 has a mutation status of G472W, The gene XKR5 has a mutation status of P600H, The gene PRSS55 has a mutation status of N203KfsTer39, The gene FGFR1 has a mutation status of G194C, The gene POTEA has a mutation status of A72G, The gene CYP7A1 has a mutation status of M227I, The gene ASPH has a mutation status of E200K, The gene TRHR has a mutation status of Y103C, The gene TRAPPC9 has a mutation status of R902L, The gene PTP4A3 has a mutation status of E127D, The gene RUSC2 has a mutation status of H626N, The gene NXNL2 has a mutation status of L5M, The gene NXNL2 has a mutation status of D50Y, The gene GABBR2 has a mutation status of Y531D, The gene ZNF618 has a mutation status of P306L, The gene PIP5KL1 has a mutation status of G126V, The gene SWI5 has a mutation status of L7F, The gene HMCN2 has a mutation status of E3470D, The gene PRRC2B has a mutation status of P2168A, The gene SARDH has a mutation status of G89V, The gene SNAPC4 has a mutation status of H860N, The gene PMPCA has a mutation status of G273V, The gene ABCA2 has a mutation status of A1451P, The gene MT-ND1 has a mutation status of T73A, The gene MT-ND3 has a mutation status of I96T, The gene MT-ND5 has a mutation status of Y159H, The gene MT-ND5 has a mutation status of T556A, The gene ARSL has a mutation status of G502W, The gene STS has a mutation status of L288M, The gene SHROOM2 has a mutation status of P1178H, The gene CDKL5 has a mutation status of T431A, The gene KLHL15 has a mutation status of T461S, The gene MAOA has a mutation status of Q418K, The gene MAOB has a mutation status of M1?, The gene SLC9A7 has a mutation status of R117M, The gene CLCN5 has a mutation status of Q194K, The gene IQSEC2 has a mutation status of P1187T, The gene IQSEC2 has a mutation status of P552Q, The gene HUWE1 has a mutation status of G1196R, The gene AMER1 has a mutation status of R621M, The gene NLGN3 has a mutation status of P87T, The gene RNF128 has a mutation status of G91V, The gene COL4A5 has a mutation status of P196H, The gene SLITRK2 has a mutation status of K252Ter	LAML
The gene EXOSC10 has a mutation status of I191NfsTer3, The gene MACF1 has a mutation status of D3218Y, The gene IPO13 has a mutation status of N41K, The gene DPH2 has a mutation status of A137V, The gene TUT4 has a mutation status of V1369I, The gene SPAG17 has a mutation status of S1242C, The gene DCST2 has a mutation status of Y358HfsTer3, The gene LAMC1 has a mutation status of G45W, The gene CFHR5 has a mutation status of R435Ter, The gene MDM4 has a mutation status of D375C, The gene KLF6 has a mutation status of S177G, The gene CUBN has a mutation status of G596C, The gene CFAP58 has a mutation status of K312R, The gene WDR11 has a mutation status of R1099H, The gene PRR33 has a mutation status of P232S, The gene ALX4 has a mutation status of P199S, The gene MS4A14 has a mutation status of S215G, The gene CD5 has a mutation status of H461C, The gene TPCN2 has a mutation status of V604F, The gene FAT3 has a mutation status of F4052S, The gene ATM has a mutation status of R2832C, The gene KDM5A has a mutation status of R519K, The gene KIF21A has a mutation status of D313E, The gene KMT2D has a mutation status of A1598V, The gene LRRIQ1 has a mutation status of K244I, The gene CEP290 has a mutation status of Q853H, The gene ANAPC5 has a mutation status of W29R, The gene TTC6 has a mutation status of V1784I, The gene SERPINA9 has a mutation status of V272D, The gene CCNK has a mutation status of K137Q, The gene AHNAK2 has a mutation status of K1107M, The gene EMC4 has a mutation status of R108Ter, The gene TYRO3 has a mutation status of K235AfsTer18, The gene SPPL2A has a mutation status of T157I, The gene SGF29 has a mutation status of R115H, The gene ZNF747 has a mutation status of G262R, The gene KIFC3 has a mutation status of K355N, The gene PKD1L2 has a mutation status of D1583E, The gene RPL26 has a mutation status of R84L, The gene CCDC178 has a mutation status of E754K, The gene MISP has a mutation status of D46E, The gene ZNRF4 has a mutation status of R177H, The gene PSG3 has a mutation status of P3T, The gene CA11 has a mutation status of D322Y, The gene IGKJ1 has a mutation status of W2Ter, The gene IL18R1 has a mutation status of P272S, The gene SLC9A4 has a mutation status of Q728Ter, The gene BAZ2B has a mutation status of R1876T, The gene KCTD18 has a mutation status of L107F, The gene RETREG2 has a mutation status of E34Ter, The gene RETREG2 has a mutation status of S37I, The gene MMP24 has a mutation status of G424S, The gene MMP24 has a mutation status of A427T, The gene SAMSN1 has a mutation status of Y130H, The gene TMPRSS15 has a mutation status of D620H, The gene TNRC6B has a mutation status of P76L, The gene SLC6A11 has a mutation status of R292Q, The gene COL7A1 has a mutation status of G905V, The gene MST1R has a mutation status of V323WfsTer15, The gene XRN1 has a mutation status of I317V, The gene LAP3 has a mutation status of R11EfsTer2, The gene PHOX2B has a mutation status of M21L, The gene PCDH10 has a mutation status of V363L, The gene MGARP has a mutation status of E178K, The gene CDH12 has a mutation status of R774H, The gene CDH6 has a mutation status of N723S, The gene AGXT2 has a mutation status of E456V, The gene PCDHGA12 has a mutation status of D128N, The gene HLA-A has a mutation status of I121R, The gene PKHD1 has a mutation status of T1592A, The gene ADGRG6 has a mutation status of N143S, The gene FBXL18 has a mutation status of G626S, The gene HOXA2 has a mutation status of A116V, The gene ZNF655 has a mutation status of F138L, The gene MUC3A has a mutation status of S2495L, The gene TRIM56 has a mutation status of A440V, The gene ASH2L has a mutation status of I394L, The gene MOS has a mutation status of R246C, The gene RECQL4 has a mutation status of S1031N, The gene HMCN2 has a mutation status of A1888E, The gene RAI2 has a mutation status of Q521R, The gene ZNF157 has a mutation status of K78Ter, The gene ARMCX6 has a mutation status of T76N, The gene TEX13A has a mutation status of H100R, The gene NLGN4Y has a mutation status of V363A	DLBC
The gene VWA1 has a mutation status of P429A, The gene DLGAP3 has a mutation status of P575L, The gene CLSPN has a mutation status of P322S, The gene DOCK7 has a mutation status of V1491L, The gene MAEL has a mutation status of L313F, The gene RGS21 has a mutation status of Q29E, The gene CENPF has a mutation status of N287S, The gene OBSCN has a mutation status of G7531E, The gene FZD8 has a mutation status of N152T, The gene PPRC1 has a mutation status of M1016L, The gene PSMD13 has a mutation status of K329Q, The gene DUSP8 has a mutation status of G572C, The gene DNHD1 has a mutation status of M809I, The gene PDE3B has a mutation status of T209S, The gene C2CD3 has a mutation status of D1575H, The gene CEP295 has a mutation status of T864R, The gene MMP7 has a mutation status of W32Ter, The gene POU2AF3 has a mutation status of C172Y, The gene TAS2R31 has a mutation status of R295W, The gene GYS2 has a mutation status of D418N, The gene MUC19 has a mutation status of T3551A, The gene MUC19 has a mutation status of Ter4378_S4379delinsWG, The gene MUC19 has a mutation status of N5779D, The gene KRT18 has a mutation status of L259R, The gene AMHR2 has a mutation status of W65G, The gene METTL25 has a mutation status of A595V, The gene FBRSL1 has a mutation status of S641G, The gene RNF17 has a mutation status of E191Q, The gene SLC15A1 has a mutation status of V450I, The gene TRAV38-2DV8 has a mutation status of T25SfsTer14, The gene TGM1 has a mutation status of M149T, The gene ZFYVE26 has a mutation status of K384N, The gene SERPINA6 has a mutation status of A399E, The gene IGHG1 has a mutation status of L192V, The gene SLC12A1 has a mutation status of V677I, The gene DAPK2 has a mutation status of F2S, The gene ZFAND6 has a mutation status of V168I, The gene ALPK3 has a mutation status of M1?, The gene ACAN has a mutation status of P1696L, The gene MCTP2 has a mutation status of V857A, The gene ZNF843 has a mutation status of W336R, The gene PIEZO1 has a mutation status of Y1680S, The gene DPEP1 has a mutation status of M111L, The gene TP53 has a mutation status of K132R, The gene DNAH9 has a mutation status of S856Y, The gene LRRC3C has a mutation status of E207D, The gene ARHGAP27 has a mutation status of A243T, The gene RBFOX3 has a mutation status of I311S, The gene EIF4A3 has a mutation status of T4_T9du, The gene TUBB8B has a mutation status of P305S, The gene DOT1L has a mutation status of R853C, The gene ARHGEF18 has a mutation status of C648R, The gene CLEC4G has a mutation status of E120K, The gene PRR36 has a mutation status of E72D, The gene MUC16 has a mutation status of T13896S, The gene PIN1 has a mutation status of V150M, The gene DNM2 has a mutation status of P195L, The gene MYO9B has a mutation status of V414I, The gene OCEL1 has a mutation status of A37T, The gene KMT2B has a mutation status of E1034A, The gene ZNF285 has a mutation status of V239L, The gene ZNF541 has a mutation status of P368R, The gene ZNF347 has a mutation status of G140D, The gene LILRB3 has a mutation status of W205Q, The gene APOB has a mutation status of Y1200Ter, The gene ABCG5 has a mutation status of A633V, The gene ERMN has a mutation status of S173C, The gene HOXD9 has a mutation status of V100G, The gene WNT6 has a mutation status of N297T, The gene CRYBA2 has a mutation status of G118S, The gene SLC4A3 has a mutation status of A668V, The gene KLHL30 has a mutation status of F162S, The gene ASXL1 has a mutation status of R693Ter, The gene MYH7B has a mutation status of R1182W, The gene PLCG1 has a mutation status of H395P, The gene PLCG1 has a mutation status of T396P, The gene ADNP has a mutation status of L868F, The gene ZNF831 has a mutation status of L906Q, The gene TRPM2 has a mutation status of E1149Ter, The gene CLTCL1 has a mutation status of A1247D, The gene DEPDC5 has a mutation status of N1216T, The gene PDXP has a mutation status of N60S, The gene SULT4A1 has a mutation status of K34T, The gene ZBED4 has a mutation status of R935C, The gene SBF1 has a mutation status of F41V, The gene MUC4 has a mutation status of P3776S, The gene MUC4 has a mutation status of P2070V, The gene TEC has a mutation status of V465L, The gene AFP has a mutation status of Y185H, The gene PKD2 has a mutation status of E117D, The gene NFKB1 has a mutation status of D958H, The gene ADAMTS6 has a mutation status of I830V, The gene MYOZ3 has a mutation status of F109V, The gene LSM11 has a mutation status of V86G, The gene ECI2 has a mutation status of E350GfsTer14, The gene HLA-A has a mutation status of Y51SfsTer34, The gene HLA-B has a mutation status of Q94_A95delinsHS, The gene HLA-DQA1 has a mutation status of E73L, The gene RRP36 has a mutation status of G162E, The gene PAQR8 has a mutation status of V266M, The gene REV3L has a mutation status of I596L, The gene DACT2 has a mutation status of F674V, The gene CCM2 has a mutation status of G8S, The gene ADCY1 has a mutation status of M1?, The gene VSTM2A has a mutation status of S24T, The gene BRI3 has a mutation status of N15H, The gene PPP1R35 has a mutation status of E132D, The gene TRBV5-7 has a mutation status of L11P, The gene GIMAP7 has a mutation status of W54G, The gene PLEC has a mutation status of E637K, The gene TAF1L has a mutation status of G1287C, The gene OBP2B has a mutation status of G27R, The gene CSF2RA has a mutation status of T242A, The gene FGD1 has a mutation status of Q956P, The gene PGRMC1 has a mutation status of C38G	LAML
The gene KIF1B has a mutation status of R1027Q, The gene UBR4 has a mutation status of S3356LfsTer41, The gene DOCK7 has a mutation status of L844R, The gene SLC44A3 has a mutation status of T401S, The gene SLC6A17 has a mutation status of D56N, The gene RPS6KC1 has a mutation status of Q740Ter, The gene OR2L2 has a mutation status of S8L, The gene BMPR1A has a mutation status of W271R, The gene CC2D2B has a mutation status of V693G, The gene ADRB1 has a mutation status of S186P, The gene MUC5B has a mutation status of I4642V, The gene OR52K2 has a mutation status of H133N, The gene OSBP has a mutation status of I600T, The gene FOXM1 has a mutation status of F758L, The gene MUC19 has a mutation status of R4223N, The gene MUC19 has a mutation status of I6366K, The gene KRT75 has a mutation status of Q143Ter, The gene ULK1 has a mutation status of D700G, The gene SACS has a mutation status of N2295K, The gene SACS has a mutation status of S2273Ter, The gene SACS has a mutation status of S2265C, The gene OR4N5 has a mutation status of C240Y, The gene SYNE2 has a mutation status of L1898P, The gene TDRD9 has a mutation status of V743L, The gene HEXA has a mutation status of M401EfsTer29, The gene NPRL3 has a mutation status of S341R, The gene ITPRIPL2 has a mutation status of T288P, The gene ZNF423 has a mutation status of T177P, The gene RFWD3 has a mutation status of S758N, The gene TRARG1 has a mutation status of K36R, The gene DHX33 has a mutation status of G253S, The gene MYH4 has a mutation status of D957N, The gene DNAH9 has a mutation status of S835Y, The gene NF1 has a mutation status of F1247IfsTer18, The gene NF1 has a mutation status of K1444M, The gene EFTUD2 has a mutation status of D273Y, The gene TRIM37 has a mutation status of N144S, The gene MTCL1 has a mutation status of A276E, The gene CABLES1 has a mutation status of S432C, The gene RIOK3 has a mutation status of S247C, The gene PARD6G has a mutation status of G226A, The gene ZNF726 has a mutation status of H191N, The gene ZNF229 has a mutation status of Q16K, The gene TOMM40 has a mutation status of L265W, The gene SIGLEC11 has a mutation status of V161I, The gene NLRP13 has a mutation status of L356Q, The gene FSHR has a mutation status of Q437Ter, The gene ANKRD36 has a mutation status of R405S, The gene RAB6D has a mutation status of K144Q, The gene SLC4A3 has a mutation status of D867P, The gene ZNF831 has a mutation status of D1530E, The gene CELSR1 has a mutation status of A716T, The gene EPHA3 has a mutation status of K500N, The gene MYLK has a mutation status of A1762V, The gene ZXDC has a mutation status of S753T, The gene MASP1 has a mutation status of I485L, The gene RASL11B has a mutation status of V183A, The gene EXOC1L has a mutation status of S18L, The gene UGT2B11 has a mutation status of E301Ter, The gene PPP3CA has a mutation status of R217Ter, The gene TAF11L11 has a mutation status of A9P, The gene PTGER4 has a mutation status of F348L, The gene PCDHB13 has a mutation status of A719V, The gene SAP30L has a mutation status of V143M, The gene ZNF354C has a mutation status of R404G, The gene CDKAL1 has a mutation status of A115G, The gene SCUBE3 has a mutation status of A241S, The gene CRISP1 has a mutation status of T97N, The gene L3MBTL3 has a mutation status of I388F, The gene DACT2 has a mutation status of L518M, The gene TAX1BP1 has a mutation status of E321V, The gene POM121L12 has a mutation status of F229L, The gene SEMA3A has a mutation status of V435I, The gene RBM48 has a mutation status of H356Y, The gene MUC3A has a mutation status of M384T, The gene RNF133 has a mutation status of G156A, The gene SLC18A1 has a mutation status of M1?, The gene EPHX2 has a mutation status of S544Y, The gene PMP2 has a mutation status of M21V, The gene DOCK8 has a mutation status of Q386Ter, The gene SPATA31D1 has a mutation status of G997W, The gene TDRD7 has a mutation status of W932Ter, The gene NANS has a mutation status of S294P, The gene MT-ND5 has a mutation status of A475T, The gene ARSF has a mutation status of G347R, The gene ATRX has a mutation status of N564S	GBMLGG
The gene CASZ1 has a mutation status of G1510D, The gene AHDC1 has a mutation status of P986S, The gene ASB17 has a mutation status of N86I, The gene MIGA1 has a mutation status of R563S, The gene CCDC18 has a mutation status of K1176E, The gene LRRC39 has a mutation status of G94D, The gene SORT1 has a mutation status of V135I, The gene CHIA has a mutation status of L94P, The gene BCL9 has a mutation status of M661L, The gene TDRKH has a mutation status of V48I, The gene OR10R2 has a mutation status of M110V, The gene ZNF678 has a mutation status of V413G, The gene OPN3 has a mutation status of F276S, The gene GATA3 has a mutation status of A396T, The gene NSUN6 has a mutation status of E236D, The gene SKIDA1 has a mutation status of N705H, The gene SCART1 has a mutation status of S637Ter, The gene UBQLNL has a mutation status of L414I, The gene SCUBE2 has a mutation status of R557L, The gene NAALADL1 has a mutation status of W237R, The gene SF3B2 has a mutation status of P6S, The gene SSH3 has a mutation status of W476G, The gene FCHSD2 has a mutation status of I104T, The gene ARHGEF17 has a mutation status of R433Q, The gene SLCO2B1 has a mutation status of V353M, The gene KLRC4 has a mutation status of S32L, The gene SUOX has a mutation status of E345Q, The gene GALNT9 has a mutation status of D68G, The gene SERPINE3 has a mutation status of L123V, The gene RBM26 has a mutation status of Q526K, The gene GAS6 has a mutation status of R594W, The gene GAS6 has a mutation status of D591E, The gene ARMH4 has a mutation status of A89T, The gene MYO1E has a mutation status of D724E, The gene HERC1 has a mutation status of A575S, The gene PARP16 has a mutation status of L72Q, The gene NPTN has a mutation status of A237T, The gene BLM has a mutation status of L107FfsTer36, The gene MSLNL has a mutation status of P175S, The gene RPGRIP1L has a mutation status of S976P, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene TP53 has a mutation status of G266R, The gene DNAH9 has a mutation status of L1462del, The gene CENPV has a mutation status of A46T, The gene MYO15A has a mutation status of G2418R, The gene MRM1 has a mutation status of V149P, The gene MED16 has a mutation status of D715N, The gene COL5A3 has a mutation status of D892G, The gene OR10H1 has a mutation status of P138R, The gene MVB12A has a mutation status of Y256C, The gene ANKRD27 has a mutation status of C440Y, The gene ZNF850 has a mutation status of K452R, The gene FCGBP has a mutation status of N1007T, The gene CCDC97 has a mutation status of V306I, The gene NLRP11 has a mutation status of L81I, The gene COBLL1 has a mutation status of S1075I, The gene XIRP2 has a mutation status of P252S, The gene TTN has a mutation status of V10101A, The gene OBSL1 has a mutation status of P860S, The gene D2HGDH has a mutation status of P492R, The gene CST3 has a mutation status of G30D, The gene SLC25A1 has a mutation status of N110S, The gene GP1BB has a mutation status of P18Q, The gene SCN11A has a mutation status of I588T, The gene ULK4 has a mutation status of S292G, The gene USP19 has a mutation status of P1231S, The gene KBTBD8 has a mutation status of V469M, The gene ZNF717 has a mutation status of G671R, The gene NAAA has a mutation status of P215L, The gene JMY has a mutation status of K633T, The gene DCTN4 has a mutation status of A177V, The gene PRPF4B has a mutation status of P432L, The gene NUP153 has a mutation status of C871Y, The gene ZNF165 has a mutation status of C461R, The gene HLA-A has a mutation status of H117Q, The gene HLA-B has a mutation status of A93R, The gene RRP36 has a mutation status of R17L, The gene TNFAIP3 has a mutation status of S649A, The gene NHSL1 has a mutation status of P995T, The gene TNRC18 has a mutation status of A227V, The gene MUC3A has a mutation status of K350E, The gene MUC3A has a mutation status of S356V, The gene WEE2 has a mutation status of K43N, The gene SGCZ has a mutation status of T235S, The gene CNGB3 has a mutation status of A663V, The gene ATAD2 has a mutation status of K1117R, The gene ZNF7 has a mutation status of T329R, The gene C5 has a mutation status of R1634W, The gene HMCN2 has a mutation status of A1668S, The gene RALGDS has a mutation status of S699T, The gene CAMSAP1 has a mutation status of H969R, The gene MT-CYB has a mutation status of I78T, The gene CACNA1F has a mutation status of G1879E, The gene CACNA1F has a mutation status of S1877I, The gene CCDC22 has a mutation status of Q308R, The gene PLXNB3 has a mutation status of S1854LfsTer53, The gene KDM5D has a mutation status of K922N	LAML
The gene CTRC has a mutation status of W164DfsTer7, The gene CLIC4 has a mutation status of K60GfsTer18, The gene MRPL37 has a mutation status of A325T, The gene LRRC8B has a mutation status of Y104C, The gene SLC6A17 has a mutation status of K603Q, The gene GJA5 has a mutation status of S357Ter, The gene NPR1 has a mutation status of Q298AfsTer18, The gene LAD1 has a mutation status of S453G, The gene PLEKHA6 has a mutation status of E877Q, The gene NUCKS1 has a mutation status of P180R, The gene OTUD1 has a mutation status of S326C, The gene SFTPD has a mutation status of Q126R, The gene DPYSL4 has a mutation status of A60T, The gene C12orf57 has a mutation status of M36L, The gene A2M has a mutation status of L818F, The gene SLC38A1 has a mutation status of P290L, The gene IFT88 has a mutation status of L534P, The gene CDX2 has a mutation status of V3M, The gene LRRC63 has a mutation status of R520S, The gene LMO7 has a mutation status of E1405D, The gene OR4Q3 has a mutation status of L113I, The gene CDH24 has a mutation status of I556T, The gene AHNAK2 has a mutation status of V2471L, The gene AHNAK2 has a mutation status of N2143D, The gene ALPK3 has a mutation status of P1124S, The gene ADAMTS18 has a mutation status of A374S, The gene ZBTB4 has a mutation status of S893P, The gene SPACA3 has a mutation status of T185I, The gene MMP28 has a mutation status of P453S, The gene KRT10 has a mutation status of G565_H566insGYGGGSSSGGGYGGGSSSGG, The gene CNTNAP1 has a mutation status of E293K, The gene SLC26A11 has a mutation status of L342M, The gene GAREM1 has a mutation status of P417S, The gene INO80C has a mutation status of A25D, The gene FHOD3 has a mutation status of E809Ter, The gene GRIN3B has a mutation status of I770T, The gene RPL36 has a mutation status of M7V, The gene FBN3 has a mutation status of A2258D, The gene MUC16 has a mutation status of T13896S, The gene SLC5A5 has a mutation status of E640D, The gene ZNF99 has a mutation status of R436L, The gene IRF2BP1 has a mutation status of S371C, The gene SULT6B1 has a mutation status of G163S, The gene SPEG has a mutation status of G1267S, The gene ANKEF1 has a mutation status of L659I, The gene RBL1 has a mutation status of V302M, The gene CDH4 has a mutation status of N302H, The gene NRIP1 has a mutation status of D174H, The gene ITSN1 has a mutation status of F961C, The gene TMEM121B has a mutation status of W318C, The gene KIAA1671 has a mutation status of S1265Y, The gene TNFSF10 has a mutation status of S133R, The gene MUC4 has a mutation status of D3781I, The gene CC2D2A has a mutation status of R92K, The gene RASGEF1B has a mutation status of W61Ter, The gene DSPP has a mutation status of D1116N, The gene DDIT4L has a mutation status of Q70P, The gene FGG has a mutation status of A383P, The gene MARCHF1 has a mutation status of S278I, The gene WDR17 has a mutation status of R640S, The gene COMMD10 has a mutation status of R36Q, The gene SEC24A has a mutation status of L470W, The gene NEUROG1 has a mutation status of S23F, The gene SH3TC2 has a mutation status of Q86K, The gene PDGFRB has a mutation status of Q519H, The gene LARP1 has a mutation status of S324I, The gene HAVCR2 has a mutation status of A251E, The gene RIPK1 has a mutation status of A569V, The gene CAP2 has a mutation status of K380N, The gene HLA-DQB2 has a mutation status of V37Y, The gene PKHD1 has a mutation status of Q960K, The gene DST has a mutation status of M1612I, The gene PHIP has a mutation status of S1207IfsTer18, The gene HOXA3 has a mutation status of D8Y, The gene IGFBP1 has a mutation status of Y254Ter, The gene ZNF107 has a mutation status of P760A, The gene ANKIB1 has a mutation status of P181L, The gene OR2AE1 has a mutation status of S214Y, The gene MUC3A has a mutation status of Y1992C, The gene ZNF777 has a mutation status of Y318F, The gene TMEM176B has a mutation status of T91P, The gene PREX2 has a mutation status of Q765H, The gene OC90 has a mutation status of W65Ter, The gene RANBP6 has a mutation status of C274R, The gene PRSS3 has a mutation status of D102I, The gene EXOSC3 has a mutation status of K209N, The gene SURF6 has a mutation status of A6V, The gene MT-ND5 has a mutation status of T544A, The gene ZNF630 has a mutation status of Y431C, The gene HUWE1 has a mutation status of Q3378L, The gene ZXDA has a mutation status of K318Q, The gene PSMD10 has a mutation status of D86E, The gene COL4A6 has a mutation status of L122M, The gene PRRG3 has a mutation status of E54A	DLBC
The gene CHD5 has a mutation status of I736V, The gene WNT4 has a mutation status of S286R, The gene TUT4 has a mutation status of A77T, The gene PGM1 has a mutation status of A403T, The gene UFC1 has a mutation status of D152E, The gene UHMK1 has a mutation status of S264N, The gene RPS6KC1 has a mutation status of S144Ter, The gene SFMBT2 has a mutation status of E791D, The gene NSUN6 has a mutation status of F39I, The gene BICC1 has a mutation status of G30D, The gene TBATA has a mutation status of Q86L, The gene CC2D2B has a mutation status of F534L, The gene FBXW4 has a mutation status of T152K, The gene CALHM1 has a mutation status of L198WfsTer57, The gene UBQLNL has a mutation status of D68N, The gene OR52B2 has a mutation status of V70L, The gene CDC42BPG has a mutation status of D23H, The gene SPDYC has a mutation status of R177W, The gene ETS1 has a mutation status of L290F, The gene MUC19 has a mutation status of T2437K, The gene TBC1D30 has a mutation status of A151S, The gene CIT has a mutation status of A1875D, The gene ZNF219 has a mutation status of H206Y, The gene TOX4 has a mutation status of Q458K, The gene PATL2 has a mutation status of Q181K, The gene SCG3 has a mutation status of G426Ter, The gene ZNF609 has a mutation status of G477V, The gene RASGRF1 has a mutation status of R130K, The gene OR4F15 has a mutation status of N202S, The gene DNAH3 has a mutation status of M2005V, The gene USP31 has a mutation status of A58V, The gene SLC38A7 has a mutation status of R237K, The gene MTSS2 has a mutation status of A726P, The gene ABR has a mutation status of D269N, The gene TCAP has a mutation status of V10L, The gene ANKRD12 has a mutation status of R1302Ter, The gene HCN2 has a mutation status of E412Ter, The gene ZFR2 has a mutation status of R523K, The gene FBN3 has a mutation status of P2029L, The gene ZNF529 has a mutation status of G540E, The gene ZNF461 has a mutation status of D10Y, The gene FCGBP has a mutation status of G1230_P1231del, The gene FCGBP has a mutation status of S1228MfsTer5, The gene SMG9 has a mutation status of S346TfsTer2, The gene RSPH6A has a mutation status of L604V, The gene NLRP12 has a mutation status of G536D, The gene LILRB1 has a mutation status of Q401L, The gene HAAO has a mutation status of P20S, The gene AQP7B has a mutation status of L289R, The gene MYO7B has a mutation status of A1406G, The gene TTN has a mutation status of S3213C, The gene CFAP65 has a mutation status of Y1074H, The gene BFSP1 has a mutation status of P586S, The gene PTPRT has a mutation status of L490E, The gene TTC3 has a mutation status of S455G, The gene MX2 has a mutation status of Q32L, The gene C2CD2 has a mutation status of D546V, The gene PHETA2 has a mutation status of R41Ter, The gene SCUBE1 has a mutation status of S447N, The gene ZBED4 has a mutation status of M981V, The gene PLXNB1 has a mutation status of A825T, The gene AMT has a mutation status of Y369Ter, The gene NPRL2 has a mutation status of N374D, The gene MANF has a mutation status of L144V, The gene STAG1 has a mutation status of K293N, The gene MECOM has a mutation status of A177E, The gene VWA5B2 has a mutation status of A369V, The gene MUC4 has a mutation status of V4009L, The gene HMX1 has a mutation status of S272P, The gene LRRC66 has a mutation status of I234V, The gene CPLANE1 has a mutation status of W1541Ter, The gene GDNF has a mutation status of R168G, The gene TCF7 has a mutation status of K98R, The gene TRIM7 has a mutation status of V418M, The gene TAP1 has a mutation status of W737Ter, The gene DNPH1 has a mutation status of P170RfsTer7, The gene COL12A1 has a mutation status of A2612S, The gene IMPG1 has a mutation status of M54I, The gene TCP1 has a mutation status of I112V, The gene LFNG has a mutation status of V115D, The gene FBXL18 has a mutation status of G156S, The gene FERD3L has a mutation status of R27C, The gene ZAN has a mutation status of G2627R, The gene EPHB6 has a mutation status of M16G, The gene EPHB6 has a mutation status of V17G, The gene XKR6 has a mutation status of T62P, The gene ZNF703 has a mutation status of S174Ter, The gene NKX6-3 has a mutation status of I58S, The gene ZNF367 has a mutation status of D141V, The gene CAMSAP1 has a mutation status of V78L, The gene CCDC187 has a mutation status of A1090E, The gene RNF224 has a mutation status of T46N	SARC
The gene SPEN has a mutation status of A3248P, The gene ARHGEF10L has a mutation status of Q914L, The gene IFFO2 has a mutation status of N61I, The gene PLK3 has a mutation status of N507S, The gene STRIP1 has a mutation status of A40E, The gene SPTA1 has a mutation status of S1066Y, The gene MYOC has a mutation status of D478Y, The gene UTP25 has a mutation status of S112I, The gene ATRNL1 has a mutation status of N681Y, The gene EMX2 has a mutation status of A5S, The gene PDE3B has a mutation status of L92M, The gene MAP6 has a mutation status of P149L, The gene IL18 has a mutation status of E192Ter, The gene CBL has a mutation status of L209V, The gene OR10G7 has a mutation status of D265H, The gene CERS5 has a mutation status of P52T, The gene LGR5 has a mutation status of L448I, The gene DENR has a mutation status of A51T, The gene CCDC122 has a mutation status of H135Y, The gene TRAV23DV6 has a mutation status of R79N, The gene VASH1 has a mutation status of R203C, The gene AHNAK2 has a mutation status of D2436E, The gene IGHV3-64D has a mutation status of A69V, The gene IGHV3-64D has a mutation status of M53I, The gene DUOX2 has a mutation status of I550T, The gene VPS13C has a mutation status of V1056I, The gene RBL2 has a mutation status of I634L, The gene TLE7 has a mutation status of G14E, The gene DNAAF1 has a mutation status of L227F, The gene GUCY2D has a mutation status of L697I, The gene RARA has a mutation status of R364Q, The gene AOC2 has a mutation status of F333S, The gene TMEM101 has a mutation status of A62V, The gene ANKRD30B has a mutation status of V221D, The gene RBBP8 has a mutation status of R536G, The gene ZNF532 has a mutation status of L164S, The gene PLK5 has a mutation status of R257S, The gene MUC16 has a mutation status of P14438T, The gene FCGBP has a mutation status of A1165GfsTer13, The gene FCGBP has a mutation status of E1160GfsTer144, The gene RALB has a mutation status of E106K, The gene ABCA12 has a mutation status of E444G, The gene SNED1 has a mutation status of H614Q, The gene ANGPT4 has a mutation status of W453L, The gene SMOX has a mutation status of V328M, The gene ADRA1D has a mutation status of E12K, The gene IGLV4-60 has a mutation status of S74F, The gene IGLV4-60 has a mutation status of N78T, The gene FOXRED2 has a mutation status of S4F, The gene CACNA1I has a mutation status of E1024D, The gene ACVR2B has a mutation status of Y410Ter, The gene LIMD1 has a mutation status of S304T, The gene CCR5 has a mutation status of M100T, The gene ITIH3 has a mutation status of F3L, The gene MAGI1 has a mutation status of L1126M, The gene DCBLD2 has a mutation status of A29S, The gene PARP14 has a mutation status of S50N, The gene ATP13A5 has a mutation status of S535T, The gene FRAS1 has a mutation status of R2362Q, The gene MSH3 has a mutation status of C833W, The gene C6orf132 has a mutation status of A690V, The gene C6orf132 has a mutation status of P672T, The gene GABRR2 has a mutation status of R69Ter, The gene VTA1 has a mutation status of P9L, The gene EPM2A has a mutation status of E19Ter, The gene MTHFD1L has a mutation status of Q11K, The gene IL6 has a mutation status of Q103R, The gene GIGYF1 has a mutation status of G19D, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of E725K, The gene PRRT4 has a mutation status of E88Ter, The gene ZNF596 has a mutation status of D173Ter, The gene SGCZ has a mutation status of Q278E, The gene ADAMDEC1 has a mutation status of K49NfsTer32, The gene SEC16A has a mutation status of G2253V, The gene MT-ND5 has a mutation status of A162T, The gene WDR44 has a mutation status of P277S	LAML
The gene ARNT has a mutation status of Q162H, The gene EFNA3 has a mutation status of C110Y, The gene SLAMF7 has a mutation status of D266S, The gene LMX1A has a mutation status of R313L, The gene SVIL has a mutation status of K831Ter, The gene GPR26 has a mutation status of D219N, The gene ZNF511 has a mutation status of C87F, The gene MUC5AC has a mutation status of A5353K, The gene OR51B2 has a mutation status of S312G, The gene CARNS1 has a mutation status of A443V, The gene EED has a mutation status of D237E, The gene CBL has a mutation status of R420Q, The gene ARHGAP32 has a mutation status of E632G, The gene NECAP1 has a mutation status of S122T, The gene SLITRK6 has a mutation status of C31Y, The gene OR4Q3 has a mutation status of L113I, The gene TRAV8-6 has a mutation status of A8T, The gene VSX2 has a mutation status of M1?, The gene VSX2 has a mutation status of G6V, The gene AHNAK2 has a mutation status of V2471L, The gene ARHGDIG has a mutation status of L13M, The gene ITGAL has a mutation status of D156V, The gene SOX15 has a mutation status of G144D, The gene MBD3L1 has a mutation status of K162N, The gene ZSWIM4 has a mutation status of T404K, The gene ZNF253 has a mutation status of T406P, The gene SPINT2 has a mutation status of A27V, The gene EPB41L5 has a mutation status of D275Y, The gene ZDBF2 has a mutation status of V1427A, The gene SLC19A3 has a mutation status of R78P, The gene OPRL1 has a mutation status of T53SfsTer33, The gene ERG has a mutation status of D345N, The gene PLXND1 has a mutation status of A370V, The gene NFKB1 has a mutation status of T585M, The gene ALPK1 has a mutation status of A331T, The gene FAT1 has a mutation status of D3258Y, The gene DNAH5 has a mutation status of A1606S, The gene CSF1R has a mutation status of Y571D, The gene ZNF300 has a mutation status of Q336H, The gene MAML1 has a mutation status of G513AfsTer27, The gene ERVFRD-1 has a mutation status of S50F, The gene SDHAF4 has a mutation status of Q46W, The gene UFL1 has a mutation status of D539KfsTer17, The gene GPER1 has a mutation status of E218P, The gene INHBA has a mutation status of A297S, The gene ELAPOR2 has a mutation status of T822I, The gene GIGYF1 has a mutation status of E139K, The gene MUC3A has a mutation status of T363M, The gene RGS22 has a mutation status of K787N, The gene TG has a mutation status of Q85H, The gene TYRP1 has a mutation status of D234Y, The gene CDKN2A has a mutation status of D74P, The gene MT-ND1 has a mutation status of G101D, The gene MT-CYB has a mutation status of T158A, The gene RPS6KA6 has a mutation status of A241P	LAML
The gene ZNF593 has a mutation status of E50A, The gene NRDC has a mutation status of A719T, The gene C8B has a mutation status of R132K, The gene USP1 has a mutation status of S704G, The gene UBQLN4 has a mutation status of G146E, The gene KLHL20 has a mutation status of L367Ter, The gene KIF21B has a mutation status of A1409G, The gene WDFY4 has a mutation status of G965E, The gene KNDC1 has a mutation status of P422L, The gene OR5D14 has a mutation status of F207S, The gene OR5B17 has a mutation status of L220_I244del, The gene GLYATL1 has a mutation status of W97C, The gene ARAP1 has a mutation status of V820L, The gene PHLDB1 has a mutation status of G1016S, The gene SORL1 has a mutation status of K214N, The gene MUC19 has a mutation status of W5287_S5346delextTer?, The gene MUC19 has a mutation status of I6366K, The gene PRPF40B has a mutation status of K567M, The gene KRT86 has a mutation status of Q139T, The gene LIN7A has a mutation status of V186A, The gene MPHOSPH9 has a mutation status of T535M, The gene PCDH9 has a mutation status of L524FfsTer8, The gene ARID4A has a mutation status of D620Y, The gene AK7 has a mutation status of P367L, The gene EIF5 has a mutation status of L46V, The gene WDR73 has a mutation status of H78N, The gene TBL3 has a mutation status of R705P, The gene FA2H has a mutation status of P112R, The gene TAOK1 has a mutation status of G957D, The gene KRTAP9-6 has a mutation status of G106C, The gene DGKE has a mutation status of E567A, The gene ANKRD30B has a mutation status of V434I, The gene FCGBP has a mutation status of P2760Q, The gene FCGBP has a mutation status of L2757P, The gene NPAS1 has a mutation status of C16W, The gene GDF7 has a mutation status of L234M, The gene SCN1A has a mutation status of A963S, The gene FZD7 has a mutation status of S358C, The gene BFSP1 has a mutation status of A36F, The gene MN1 has a mutation status of L721R, The gene LARGE1 has a mutation status of R626K, The gene ATP5MGL has a mutation status of G77R, The gene MON1A has a mutation status of A126T, The gene ZBED2 has a mutation status of G116S, The gene ZBED2 has a mutation status of G32E, The gene MUC4 has a mutation status of T2966L, The gene MUC4 has a mutation status of D2965S, The gene MUC4 has a mutation status of V2825A, The gene ZNF518B has a mutation status of V353A, The gene SH3RF1 has a mutation status of K717T, The gene EXOC3 has a mutation status of E36D, The gene HSPA4 has a mutation status of S155Ter, The gene SRA1 has a mutation status of Q154Ter, The gene BTNL8 has a mutation status of S136P, The gene ATF6B has a mutation status of P433S, The gene TBXT has a mutation status of K114QfsTer52, The gene CLCN1 has a mutation status of Q675Ter, The gene NOS3 has a mutation status of E677Ter, The gene COL14A1 has a mutation status of E1691K, The gene PLEC has a mutation status of A1471P, The gene FRMPD1 has a mutation status of I1226L, The gene IGFBPL1 has a mutation status of G173R, The gene SVEP1 has a mutation status of A3208L, The gene SH3GLB2 has a mutation status of I201S, The gene CARD9 has a mutation status of R202W, The gene CACNA1B has a mutation status of P1055R, The gene ARHGAP6 has a mutation status of I367V, The gene DIPK2B has a mutation status of R205C	SARC
The gene AGRN has a mutation status of R233H, The gene NPHP4 has a mutation status of S496Ter, The gene MYOM3 has a mutation status of E144L, The gene TRNP1 has a mutation status of V155L, The gene MACF1 has a mutation status of R5981C, The gene MPL has a mutation status of Ter636WextTer13, The gene FAAH has a mutation status of W462C, The gene TTC4 has a mutation status of H166Y, The gene RAVER2 has a mutation status of P77T, The gene MIER1 has a mutation status of E74K, The gene VCAM1 has a mutation status of E179K, The gene FLG has a mutation status of S680A, The gene NUP210L has a mutation status of E831K, The gene CCDC181 has a mutation status of R125I, The gene RGL1 has a mutation status of S744I, The gene PPP1R15B has a mutation status of P276S, The gene HHIPL2 has a mutation status of A466V, The gene OR2L2 has a mutation status of V108A, The gene IL2RA has a mutation status of E137G, The gene GPR158 has a mutation status of E1148S, The gene PHYHIPL has a mutation status of I61V, The gene NRG3 has a mutation status of E126D, The gene INPP5F has a mutation status of Q14H, The gene PWWP2B has a mutation status of P251T, The gene SIGIRR has a mutation status of W237C, The gene SIGIRR has a mutation status of R235L, The gene UBQLNL has a mutation status of M191L, The gene OR5B12 has a mutation status of P180A, The gene MEN1 has a mutation status of R516PfsTer15, The gene FAT3 has a mutation status of R2930G, The gene TMEM25 has a mutation status of P7Q, The gene VWF has a mutation status of S1930R, The gene KRAS has a mutation status of Q61H, The gene LRRK2 has a mutation status of L794V, The gene IRAK3 has a mutation status of G247R, The gene OTOGL has a mutation status of P1807Q, The gene OTOGL has a mutation status of Y1812C, The gene STARD13 has a mutation status of M862I, The gene MDGA2 has a mutation status of S692G, The gene NEK9 has a mutation status of E508K, The gene GPR68 has a mutation status of W254L, The gene ASPG has a mutation status of Q518Ter, The gene KIF26A has a mutation status of E247Ter, The gene TEDC1 has a mutation status of L360R, The gene HERC2 has a mutation status of S2422P, The gene KNL1 has a mutation status of S756L, The gene PIF1 has a mutation status of A383T, The gene PDCD7 has a mutation status of P16H, The gene PDE8A has a mutation status of R46C, The gene MEF2A has a mutation status of P471A, The gene PGAP6 has a mutation status of L278R, The gene PRR35 has a mutation status of R257S, The gene NLRC3 has a mutation status of P244T, The gene RBFOX1 has a mutation status of Q83P, The gene ZNF267 has a mutation status of K357Ter, The gene SLC9A5 has a mutation status of V63L, The gene TP53 has a mutation status of Y220C, The gene MYH1 has a mutation status of H1594R, The gene DNAH9 has a mutation status of I4264T, The gene LLGL1 has a mutation status of W409Ter, The gene PIGS has a mutation status of D246H, The gene TOP2A has a mutation status of T530A, The gene CCR7 has a mutation status of W183Ter, The gene KRTAP17-1 has a mutation status of E15G, The gene XYLT2 has a mutation status of E449K, The gene KPNA2 has a mutation status of A397G, The gene FBF1 has a mutation status of A919G, The gene UBE2O has a mutation status of D650E, The gene SLC38A10 has a mutation status of N8D, The gene ANKRD12 has a mutation status of S941G, The gene ANKRD12 has a mutation status of K948E, The gene CCDC102B has a mutation status of K105E, The gene TSHZ1 has a mutation status of H475N, The gene MFSD12 has a mutation status of Q212PfsTer202, The gene MATK has a mutation status of W415Ter, The gene SHD has a mutation status of Q324R, The gene ARRDC5 has a mutation status of C124F, The gene ANGPTL4 has a mutation status of R230L, The gene KANK2 has a mutation status of S498I, The gene RASAL3 has a mutation status of K766N, The gene CYP4F8 has a mutation status of V81L, The gene ANO8 has a mutation status of E557D, The gene SLC27A1 has a mutation status of A51E, The gene SSBP4 has a mutation status of L176I, The gene KPTN has a mutation status of A428V, The gene SCAF1 has a mutation status of P617Q, The gene NBAS has a mutation status of K1801R, The gene LRRTM1 has a mutation status of D352N, The gene PTCD3 has a mutation status of E311K, The gene LRP1B has a mutation status of E1080MfsTer114, The gene CCDC148 has a mutation status of E90Ter, The gene XIRP2 has a mutation status of P252S, The gene TTC30A has a mutation status of P633T, The gene OSBPL6 has a mutation status of L592Q, The gene PLCD4 has a mutation status of I380T, The gene SP100 has a mutation status of N257I, The gene GIGYF2 has a mutation status of G148A, The gene ANGPT4 has a mutation status of R259L, The gene SIRPA has a mutation status of S314R, The gene PTPRA has a mutation status of K239R, The gene APMAP has a mutation status of G6W, The gene DIDO1 has a mutation status of P2016A, The gene COL18A1 has a mutation status of P21H, The gene TBX1 has a mutation status of P461T, The gene IGLV3-16 has a mutation status of Q25R, The gene TOMM22 has a mutation status of P16L, The gene SELENOO has a mutation status of R424G, The gene SCN5A has a mutation status of L1215I, The gene SCN5A has a mutation status of T423I, The gene NBEAL2 has a mutation status of Q2726K, The gene PARP3 has a mutation status of W8L, The gene IFT122 has a mutation status of R1178C, The gene MUC4 has a mutation status of V3305_S3336del, The gene ADAMTS3 has a mutation status of R1143K, The gene ADH1B has a mutation status of G205S, The gene GYPE has a mutation status of T22A, The gene GLRB has a mutation status of A294T, The gene HAND2 has a mutation status of L47I, The gene TRIML2 has a mutation status of R215G, The gene NSUN2 has a mutation status of S496C, The gene UGT3A1 has a mutation status of T421A, The gene PDE4D has a mutation status of K354N, The gene FOXD1 has a mutation status of G43V, The gene BTF3 has a mutation status of A10D, The gene PCDHGA2 has a mutation status of F472S, The gene PCDHGA12 has a mutation status of G70S, The gene SH3PXD2B has a mutation status of M1?, The gene H2BC13 has a mutation status of I95RfsTer?, The gene HLA-A has a mutation status of A18D, The gene ITPR3 has a mutation status of N2564T, The gene LRRC73 has a mutation status of S293R, The gene CAPN11 has a mutation status of G171S, The gene TDRD6 has a mutation status of A1009E, The gene PKHD1 has a mutation status of N3062D, The gene ZNF292 has a mutation status of Q172K, The gene KLHL32 has a mutation status of H170Y, The gene TUBE1 has a mutation status of E198K, The gene DSE has a mutation status of R350H, The gene SNX8 has a mutation status of P438T, The gene EVX1 has a mutation status of G155R, The gene TBX20 has a mutation status of T331A, The gene PURB has a mutation status of S8I, The gene ADAM22 has a mutation status of Q771H, The gene CYP51A1 has a mutation status of K297R, The gene MUC3A has a mutation status of G307H, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of S2495L, The gene CREB3L2 has a mutation status of L138H, The gene ZNF746 has a mutation status of S632Y, The gene NUB1 has a mutation status of E570Ter, The gene KMT2C has a mutation status of Q2997Ter, The gene USP17L2 has a mutation status of V58GfsTer13, The gene ZNF703 has a mutation status of G365V, The gene RP1 has a mutation status of V944M, The gene TTPA has a mutation status of R5L, The gene EYA1 has a mutation status of D388YfsTer3, The gene ZFHX4 has a mutation status of P2053H, The gene TGFBR1 has a mutation status of N45Y, The gene ZNF883 has a mutation status of Q294K, The gene SCAI has a mutation status of A5T, The gene MT-ND5 has a mutation status of L450P, The gene MT-CYB has a mutation status of N260D, The gene DMD has a mutation status of L1162I, The gene RPGR has a mutation status of E845D, The gene MAGIX has a mutation status of V46I, The gene XAGE5 has a mutation status of E50D, The gene OGT has a mutation status of G940V, The gene TEX13D has a mutation status of P325T	PAAD
The gene PRAMEF1 has a mutation status of R213F, The gene PLA2G2A has a mutation status of K122_Y125del, The gene DMRTA2 has a mutation status of G134D, The gene C8A has a mutation status of W430Ter, The gene BCL2L15 has a mutation status of S94T, The gene VTCN1 has a mutation status of P175S, The gene SETDB1 has a mutation status of V132EfsTer3, The gene FLG has a mutation status of R3277L, The gene USH2A has a mutation status of G4106R, The gene VSTM4 has a mutation status of S56C, The gene ANK3 has a mutation status of F1348S, The gene BMPR1A has a mutation status of R120Q, The gene EPS8L2 has a mutation status of V677L, The gene PPFIBP2 has a mutation status of C699S, The gene TRIM51 has a mutation status of D318N, The gene SMTNL1 has a mutation status of G227R, The gene AHNAK has a mutation status of I1855M, The gene USP5 has a mutation status of G215F, The gene SENP1 has a mutation status of H218Y, The gene MYO1H has a mutation status of E73K, The gene SCFD1 has a mutation status of V341D, The gene AHSA1 has a mutation status of W27R, The gene MYO1E has a mutation status of T560I, The gene MAP2K5 has a mutation status of P404A, The gene CYP11A1 has a mutation status of Y238N, The gene MFGE8 has a mutation status of Q334PfsTer9, The gene TARS3 has a mutation status of L652V, The gene OR1P1 has a mutation status of T253I, The gene MPDU1 has a mutation status of A52S, The gene DHRS7C has a mutation status of L66Q, The gene LLGL1 has a mutation status of Q20E, The gene MRM1 has a mutation status of V149P, The gene KRT15 has a mutation status of E377G, The gene DGKE has a mutation status of W452Ter, The gene MARCHF10 has a mutation status of L754V, The gene GPR142 has a mutation status of P366RfsTer?, The gene NPTX1 has a mutation status of E52Ter, The gene NPTX1 has a mutation status of G50V, The gene L3MBTL4 has a mutation status of M163I, The gene PSMA8 has a mutation status of A196T, The gene ZNF397 has a mutation status of A508S, The gene ADGRE1 has a mutation status of T377A, The gene MUC16 has a mutation status of V13518L, The gene SMARCA4 has a mutation status of R1192H, The gene NOTCH3 has a mutation status of R75P, The gene ZNF99 has a mutation status of I200M, The gene ZNF91 has a mutation status of M79I, The gene ZNF816 has a mutation status of R529K, The gene FBXO41 has a mutation status of R567L, The gene GALNT13 has a mutation status of V336A, The gene XIRP2 has a mutation status of P252S, The gene NBEAL1 has a mutation status of P922H, The gene NBEAL1 has a mutation status of S928N, The gene CFAP65 has a mutation status of L1864M, The gene SRXN1 has a mutation status of L53P, The gene NSFL1C has a mutation status of I287SfsTer2, The gene NF2 has a mutation status of Q389Ter, The gene NECTIN3 has a mutation status of Y526N, The gene LRRIQ4 has a mutation status of K499M, The gene TP63 has a mutation status of D78V, The gene SNX25 has a mutation status of Q451Ter, The gene HTR1A has a mutation status of W161Ter, The gene VCAN has a mutation status of P828S, The gene WDR36 has a mutation status of L700F, The gene LVRN has a mutation status of A693D, The gene WNT8A has a mutation status of T211K, The gene ARHGEF37 has a mutation status of Q155K, The gene FAT2 has a mutation status of S1713F, The gene F13A1 has a mutation status of P384S, The gene MUC21 has a mutation status of T323V, The gene HLA-B has a mutation status of Y140L, The gene HLA-B has a mutation status of A93R, The gene TINAG has a mutation status of N399K, The gene PNISR has a mutation status of H558Q, The gene RFX6 has a mutation status of T124K, The gene HOXA1 has a mutation status of S199C, The gene CDK13 has a mutation status of G714S, The gene ABCA13 has a mutation status of A3744S, The gene DYNC1I1 has a mutation status of R241L, The gene DLD has a mutation status of T319A, The gene CTTNBP2 has a mutation status of S1596del, The gene TAS2R5 has a mutation status of Y80C, The gene TRBV7-7 has a mutation status of S81T, The gene KCNH2 has a mutation status of S951I, The gene PNMA2 has a mutation status of K202RfsTer19, The gene MPDZ has a mutation status of N128Y, The gene PHF2 has a mutation status of P988_T991du, The gene CACNA1B has a mutation status of M1756L, The gene MT-CYB has a mutation status of I153T, The gene FAM47A has a mutation status of L721F, The gene CFAP47 has a mutation status of P478S, The gene MAGED2 has a mutation status of G8L, The gene STARD8 has a mutation status of S694P, The gene KCNE5 has a mutation status of D92_E93delinsETer, The gene BCORL1 has a mutation status of P384T, The gene MAGEC2 has a mutation status of P77S, The gene IRAK1 has a mutation status of T304I	KIPAN
The gene CHD5 has a mutation status of L47H, The gene PEAR1 has a mutation status of Q957H, The gene OR52E8 has a mutation status of T139K, The gene SLC22A24 has a mutation status of H456Y, The gene PLCB3 has a mutation status of E277V, The gene RPS6KA4 has a mutation status of G346V, The gene INPPL1 has a mutation status of A902S, The gene OR4D5 has a mutation status of I277V, The gene OR8B8 has a mutation status of P79R, The gene PEX5 has a mutation status of M369RfsTer19, The gene PTHLH has a mutation status of H41Y, The gene MUC19 has a mutation status of N6618_I6619delinsSV, The gene MON2 has a mutation status of I1052F, The gene TRHDE has a mutation status of T716S, The gene KCNC2 has a mutation status of H19Q, The gene VEZT has a mutation status of I722N, The gene TDG has a mutation status of L265_Y267du, The gene RNF34 has a mutation status of E339Ter, The gene ZNF268 has a mutation status of P695S, The gene LIG4 has a mutation status of K782N, The gene CCDC177 has a mutation status of G615C, The gene ARID3B has a mutation status of R455QfsTer35, The gene NUDT16L1 has a mutation status of S162T, The gene APOBR has a mutation status of L703P, The gene TUFM has a mutation status of E335D, The gene ITGAM has a mutation status of V1020Ter, The gene TP53 has a mutation status of C176F, The gene ODAD4 has a mutation status of Q538H, The gene RBFOX3 has a mutation status of A8PfsTer45, The gene CBX4 has a mutation status of H400du, The gene RMC1 has a mutation status of I195V, The gene NFATC1 has a mutation status of E599D, The gene DNMT1 has a mutation status of Y939LfsTer13, The gene ZNF763 has a mutation status of V209F, The gene GARRE1 has a mutation status of Y850TfsTer34, The gene LRFN1 has a mutation status of E764D, The gene SUPT5H has a mutation status of D456E, The gene SUPT5H has a mutation status of E556D, The gene NAPA has a mutation status of K246NfsTer3, The gene KIR2DL4 has a mutation status of C97F, The gene ITSN2 has a mutation status of A397S, The gene CYP1B1 has a mutation status of Y249S, The gene EPAS1 has a mutation status of G686R, The gene EPCAM has a mutation status of A107T, The gene FAM161A has a mutation status of V126I, The gene FHL2 has a mutation status of I270V, The gene NYAP2 has a mutation status of S624L, The gene FASTKD5 has a mutation status of L278F, The gene PAK5 has a mutation status of P280_M282del, The gene TASP1 has a mutation status of F332I, The gene MATN4 has a mutation status of Q580E, The gene PTGIS has a mutation status of V203I, The gene ABHD16B has a mutation status of L377V, The gene NBEAL2 has a mutation status of V1515G, The gene CELSR3 has a mutation status of I893T, The gene CACNA2D2 has a mutation status of W901TfsTer14, The gene CACNA2D2 has a mutation status of Q897SfsTer16, The gene CRYBG3 has a mutation status of G1680D, The gene TMEM39A has a mutation status of L245Q, The gene GPR149 has a mutation status of V127SfsTer160, The gene STX18 has a mutation status of K46RfsTer11, The gene STX18 has a mutation status of E37_R44delinsG, The gene STIM2 has a mutation status of S523L, The gene GSX2 has a mutation status of L163F, The gene PKD2 has a mutation status of D702E, The gene TACR3 has a mutation status of C311HfsTer11, The gene DNAH5 has a mutation status of L4191P, The gene PDZD2 has a mutation status of T649I, The gene PRLR has a mutation status of V253A, The gene CPLANE1 has a mutation status of Y2728S, The gene OR2B8P has a mutation status of P287T, The gene GTF2H4 has a mutation status of H366Q, The gene TCF19 has a mutation status of V247F, The gene KCNK5 has a mutation status of Q41H, The gene RRP36 has a mutation status of P34T, The gene NOX3 has a mutation status of W481Ter, The gene FKBP6 has a mutation status of R204L, The gene FAM237B has a mutation status of M75I, The gene SLC12A9 has a mutation status of S438G, The gene MUC3A has a mutation status of V1672D, The gene ATP6V0A4 has a mutation status of S500R, The gene ZNF596 has a mutation status of N207I, The gene GFRA2 has a mutation status of A298G, The gene DMTN has a mutation status of N182K, The gene DOCK5 has a mutation status of D745N, The gene CHRNA6 has a mutation status of P58R, The gene NOL6 has a mutation status of D789G, The gene FGD3 has a mutation status of G410C, The gene FKBP15 has a mutation status of E201K, The gene MT-ND5 has a mutation status of V24I, The gene CENPVL3 has a mutation status of R12W, The gene GPRASP2 has a mutation status of S793Ter, The gene STAG2 has a mutation status of Q735Ter	SARC
The gene JUN has a mutation status of C320Y, The gene LRRIQ3 has a mutation status of K242R, The gene ASB17 has a mutation status of R234I, The gene GFI1 has a mutation status of A166V, The gene CELSR2 has a mutation status of R2015K, The gene PTGFRN has a mutation status of A182V, The gene NBPF12 has a mutation status of L1378V, The gene SPRR1B has a mutation status of K60N, The gene DENND4B has a mutation status of S1112L, The gene RUSC1 has a mutation status of A335T, The gene SMG5 has a mutation status of D319Y, The gene CENPF has a mutation status of L2756R, The gene HNRNPU has a mutation status of P724S, The gene PFKP has a mutation status of E62K, The gene TBATA has a mutation status of V47M, The gene VSIR has a mutation status of L27I, The gene MYOZ1 has a mutation status of G95E, The gene CPEB3 has a mutation status of A199E, The gene CPEB3 has a mutation status of P196H, The gene ALDH18A1 has a mutation status of L455AfsTer26, The gene TIAL1 has a mutation status of Q230H, The gene DPYSL4 has a mutation status of G441A, The gene LRRC27 has a mutation status of E359D, The gene LRRC4C has a mutation status of R175C, The gene DDIAS has a mutation status of A427E, The gene MMP1 has a mutation status of F464L, The gene KRAS has a mutation status of G12D, The gene FGD4 has a mutation status of L304I, The gene RAPGEF3 has a mutation status of R47M, The gene XPOT has a mutation status of R102Ter, The gene ABTB3 has a mutation status of D625G, The gene HERC2 has a mutation status of V1740I, The gene VPS13C has a mutation status of N642K, The gene HMG20A has a mutation status of E306G, The gene ADAMTS7 has a mutation status of D857E, The gene CHST4 has a mutation status of D110Y, The gene ATMIN has a mutation status of E67G, The gene TP53 has a mutation status of G245S, The gene MRM1 has a mutation status of V149P, The gene GJD3 has a mutation status of P244T, The gene KIF2B has a mutation status of R36L, The gene TSPOAP1 has a mutation status of V1786M, The gene HEATR6 has a mutation status of A1163D, The gene TMEM200C has a mutation status of S546C, The gene MYO1F has a mutation status of Q1013H, The gene LSM14A has a mutation status of E32D, The gene TTC9B has a mutation status of Q126K, The gene SHANK1 has a mutation status of P1593L, The gene RASGRP3 has a mutation status of P392S, The gene HEATR5B has a mutation status of A435T, The gene CCDC88A has a mutation status of Q1619H, The gene EGR4 has a mutation status of L304M, The gene SCN9A has a mutation status of Q805Ter, The gene FASTKD1 has a mutation status of K740NfsTer10, The gene CAVIN2 has a mutation status of E9Ter, The gene TRPM8 has a mutation status of A156S, The gene ACSS1 has a mutation status of R411Q, The gene CDH26 has a mutation status of Q426L, The gene MTG2 has a mutation status of Q55_E56delinsHK, The gene RTEL1 has a mutation status of S212C, The gene DOP1B has a mutation status of H1375L, The gene IL17RA has a mutation status of L26M, The gene MYO18B has a mutation status of L1941I, The gene ZKSCAN7 has a mutation status of Q149K, The gene PFKFB4 has a mutation status of R351W, The gene ADAMTS9 has a mutation status of K633T, The gene NEPRO has a mutation status of K240E, The gene KCTD8 has a mutation status of A192G, The gene ADGRL3 has a mutation status of Q64K, The gene WDFY3 has a mutation status of R3149Ter, The gene LARP1B has a mutation status of L726F, The gene FBXW7 has a mutation status of E489Ter, The gene DDX60L has a mutation status of N1055S, The gene WWC2 has a mutation status of R35W, The gene HTR1A has a mutation status of R333C, The gene ARSB has a mutation status of T107A, The gene APC has a mutation status of E1317Ter, The gene CARMIL1 has a mutation status of T375I, The gene BTN2A1 has a mutation status of T289R, The gene TNF has a mutation status of S80P, The gene HLA-DQB2 has a mutation status of V37Y, The gene GLO1 has a mutation status of S120Ter, The gene BMP5 has a mutation status of D169Y, The gene TRDN has a mutation status of D627Y, The gene MYB has a mutation status of C734G, The gene RADIL has a mutation status of M1053T, The gene ZNF853 has a mutation status of L329M, The gene SNX13 has a mutation status of K76Ter, The gene CCDC201 has a mutation status of S127Y, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of L570T, The gene MUC3A has a mutation status of A1358D, The gene LAMB1 has a mutation status of I1648_R1653del, The gene MGAM has a mutation status of W2427Ter, The gene MGAM2 has a mutation status of L254M, The gene OR6B1 has a mutation status of A258V, The gene CNTNAP2 has a mutation status of S693L, The gene CUL1 has a mutation status of E124K, The gene PREX2 has a mutation status of H446N, The gene ZFHX4 has a mutation status of K3407M, The gene IL7 has a mutation status of T112del, The gene AGO2 has a mutation status of P295L, The gene HGH1 has a mutation status of P53T, The gene MFSD3 has a mutation status of L283S, The gene MPDZ has a mutation status of T2018I, The gene ABCA1 has a mutation status of I1103V, The gene PAPPA has a mutation status of T648M, The gene DMD has a mutation status of E767K, The gene SOX3 has a mutation status of V254M	COAD
The gene ZNF436 has a mutation status of S347L, The gene TMEM54 has a mutation status of F133S, The gene KLF18 has a mutation status of A428T, The gene ZFYVE9 has a mutation status of R254K, The gene LRRC39 has a mutation status of R21KfsTer7, The gene DENND2C has a mutation status of E55GfsTer9, The gene ARHGEF2 has a mutation status of E267KfsTer32, The gene FCER1A has a mutation status of G242V, The gene ASTN1 has a mutation status of D1227Y, The gene MIA3 has a mutation status of L1085V, The gene OR52N2 has a mutation status of Y125N, The gene OR4A16 has a mutation status of K22Q, The gene OR4A16 has a mutation status of I319A, The gene OR10Q1 has a mutation status of P133L, The gene AHNAK has a mutation status of K1649R, The gene KLHL35 has a mutation status of H5R, The gene FAT3 has a mutation status of Y613Ter, The gene RPUSD4 has a mutation status of K230G, The gene RPUSD4 has a mutation status of D228EfsTer80, The gene KRT82 has a mutation status of A504D, The gene KRT6B has a mutation status of G133R, The gene OSBPL8 has a mutation status of D307E, The gene DEPDC4 has a mutation status of K171R, The gene PITPNM2 has a mutation status of R991C, The gene BORA has a mutation status of Ter560QextTer9, The gene ADPRHL1 has a mutation status of E1726G, The gene TTC6 has a mutation status of E252D, The gene HERC1 has a mutation status of A399T, The gene ITGA11 has a mutation status of D115N, The gene TICRR has a mutation status of S1074P, The gene CHD2 has a mutation status of K173Q, The gene MVP has a mutation status of P491L, The gene TP53 has a mutation status of K139RfsTer31, The gene SMIM5 has a mutation status of V45G, The gene DNAH17 has a mutation status of E2880D, The gene MTCL1 has a mutation status of A276E, The gene SALL3 has a mutation status of A185L, The gene PTPRS has a mutation status of A974S, The gene LRRC25 has a mutation status of P303S, The gene ZNF90 has a mutation status of M598I, The gene RYR1 has a mutation status of N2213H, The gene CIC has a mutation status of Q420SfsTer59, The gene CIC has a mutation status of L421RfsTer72, The gene MYH14 has a mutation status of A1616GfsTer18, The gene LILRB3 has a mutation status of V574A, The gene KIR2DL1 has a mutation status of T286S, The gene SPTBN1 has a mutation status of M133T, The gene SPTBN1 has a mutation status of R1432W, The gene DNAH6 has a mutation status of G1275V, The gene NEB has a mutation status of D7430V, The gene ADAM23 has a mutation status of V306A, The gene SLC4A3 has a mutation status of D867P, The gene GPR55 has a mutation status of F247del, The gene SNED1 has a mutation status of Q1242P, The gene TMC2 has a mutation status of G331V, The gene CFAP61 has a mutation status of K707I, The gene CASS4 has a mutation status of V500A, The gene ZNF280B has a mutation status of D337N, The gene TPST2 has a mutation status of P332L, The gene AP1B1 has a mutation status of P796T, The gene TOM1 has a mutation status of E433K, The gene KLHL18 has a mutation status of Y386C, The gene DNAH12 has a mutation status of Q1674H, The gene ROBO2 has a mutation status of A54V, The gene OSBPL11 has a mutation status of G442E, The gene EEFSEC has a mutation status of R443W, The gene MUC4 has a mutation status of V2825A, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene MUC4 has a mutation status of M1327T, The gene RBM47 has a mutation status of R137H, The gene ALPK1 has a mutation status of R1084Q, The gene FSTL5 has a mutation status of V421M, The gene MARCHF1 has a mutation status of E126Q, The gene SLC6A19 has a mutation status of L461V, The gene VCAN has a mutation status of F3308L, The gene SYNPO has a mutation status of Q431H, The gene RANBP9 has a mutation status of T443S, The gene SLC17A3 has a mutation status of N332Y, The gene HLA-DQB2 has a mutation status of V37Y, The gene FOXL3 has a mutation status of R175C, The gene MACC1 has a mutation status of D687KfsTer10, The gene NFE2L3 has a mutation status of G138E, The gene MUC3A has a mutation status of W18G, The gene VGF has a mutation status of N401K, The gene CADPS2 has a mutation status of T589A, The gene ZNF786 has a mutation status of R619G, The gene PEBP4 has a mutation status of Q221P, The gene PRSS3 has a mutation status of D102I, The gene ZNF462 has a mutation status of P103L, The gene MT-ND4 has a mutation status of F121L, The gene MT-ND5 has a mutation status of T489M, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene VCX has a mutation status of A108S, The gene DGKK has a mutation status of A114_P115insTEPA, The gene IGSF1 has a mutation status of H407Y	PRAD
The gene HES5 has a mutation status of K147_A148delinsT, The gene ARID1A has a mutation status of D2178GfsTer47, The gene PPM1J has a mutation status of R133G, The gene FLG has a mutation status of H3888Q, The gene OR10Z1 has a mutation status of A133T, The gene TP53BP2 has a mutation status of Y356C, The gene SCCPDH has a mutation status of Q31E, The gene OR2T11 has a mutation status of S170N, The gene DLG5 has a mutation status of G1782S, The gene PTEN has a mutation status of R130G, The gene HTR7 has a mutation status of R408W, The gene TACC2 has a mutation status of A1838C, The gene FOXI2 has a mutation status of R151C, The gene PWWP2B has a mutation status of G264R, The gene DCHS1 has a mutation status of L598P, The gene OLFML1 has a mutation status of E98Ter, The gene TCN1 has a mutation status of Q289Ter, The gene CD5 has a mutation status of H461C, The gene VWCE has a mutation status of C404L, The gene CNIH2 has a mutation status of F23del, The gene GRK2 has a mutation status of L243V, The gene TBC1D10C has a mutation status of S29I, The gene CARNS1 has a mutation status of R187G, The gene IFT46 has a mutation status of H163Q, The gene SCNN1A has a mutation status of R181W, The gene KRAS has a mutation status of G12C, The gene CCDC91 has a mutation status of T39N, The gene MUC19 has a mutation status of V4071A, The gene OR8S1 has a mutation status of R220C, The gene LARP4 has a mutation status of D567Y, The gene HOXC12 has a mutation status of Q164P, The gene CFAP73 has a mutation status of A186P, The gene FGF9 has a mutation status of F77I, The gene ATP8A2 has a mutation status of L624_R625delinsFW, The gene UBE2L5 has a mutation status of H119R, The gene IRS2 has a mutation status of S210C, The gene TGM1 has a mutation status of D406H, The gene ABHD12B has a mutation status of K313EfsTer5, The gene FBXO34 has a mutation status of V192L, The gene TTLL5 has a mutation status of D73G, The gene CCDC9B has a mutation status of G466Ter, The gene PEAK1 has a mutation status of S255R, The gene TP53 has a mutation status of K101NfsTer47, The gene SALL3 has a mutation status of P485R, The gene NFIC has a mutation status of A393V, The gene MUC16 has a mutation status of T13896S, The gene LILRB1 has a mutation status of Q401L, The gene ALK has a mutation status of S439R, The gene MGAT5 has a mutation status of E606K, The gene LRP2 has a mutation status of E730K, The gene ZNF337 has a mutation status of H370QfsTer17, The gene ZNF335 has a mutation status of T578M, The gene KRTAP19-5 has a mutation status of S57G, The gene UMODL1 has a mutation status of I995F, The gene TUBGCP6 has a mutation status of E788G, The gene ZNF501 has a mutation status of G196V, The gene MCM2 has a mutation status of L877F, The gene MUC4 has a mutation status of P3312S, The gene GRXCR1 has a mutation status of E187K, The gene REST has a mutation status of T205A, The gene FRAS1 has a mutation status of S2055C, The gene ANK2 has a mutation status of G2342V, The gene GAB1 has a mutation status of G231V, The gene RICTOR has a mutation status of N44Y, The gene PLCXD3 has a mutation status of D164E, The gene PARP8 has a mutation status of P366S, The gene GLRX has a mutation status of A67T, The gene GALNT10 has a mutation status of L485P, The gene FAM8A1 has a mutation status of L338I, The gene KDM1B has a mutation status of P304S, The gene HLA-C has a mutation status of P44T, The gene SLC44A4 has a mutation status of M1?, The gene HLA-DRB5 has a mutation status of Y42H, The gene HLA-DRB1 has a mutation status of D57I, The gene HLA-DRB1 has a mutation status of F55N, The gene HLA-DQA2 has a mutation status of S75R, The gene ZNF76 has a mutation status of S269Y, The gene DSE has a mutation status of S585R, The gene GRM1 has a mutation status of H54Y, The gene ADAM22 has a mutation status of K909E, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of V1672D, The gene PRKAR2B has a mutation status of N107S, The gene FAM167A has a mutation status of E170D, The gene GATA4 has a mutation status of R284H, The gene ZFHX4 has a mutation status of M1764I, The gene MTBP has a mutation status of I291M, The gene KCNV2 has a mutation status of P92H, The gene CDKN2A has a mutation status of S8NfsTer26, The gene IZUMO3 has a mutation status of G46C, The gene PRSS3 has a mutation status of D102I, The gene FRMPD1 has a mutation status of G765V, The gene RMI1 has a mutation status of G272D, The gene SLC44A1 has a mutation status of S8T, The gene SETX has a mutation status of L2463V, The gene MT-ND4 has a mutation status of G311S, The gene RAI2 has a mutation status of P202T, The gene TFE3 has a mutation status of A21SfsTer32, The gene GDI1 has a mutation status of Q346R	OV
The gene HES4 has a mutation status of D103P, The gene SPEN has a mutation status of A3248P, The gene USP48 has a mutation status of K425M, The gene MYOM3 has a mutation status of P433S, The gene PAFAH2 has a mutation status of A63D, The gene MPL has a mutation status of A490G, The gene CELSR2 has a mutation status of R2015K, The gene SPAG17 has a mutation status of S1103VfsTer24, The gene CDC42BPA has a mutation status of D1709N, The gene GNPAT has a mutation status of D361G, The gene ZNF503 has a mutation status of C427Y, The gene LIPJ has a mutation status of N86S, The gene CYP2C8 has a mutation status of M345T, The gene SORCS3 has a mutation status of Q1079K, The gene ADRA2A has a mutation status of R263L, The gene DNHD1 has a mutation status of P4422S, The gene C1QTNF4 has a mutation status of G22S, The gene CABP4 has a mutation status of M205R, The gene OR8G3P has a mutation status of V39M, The gene ROBO4 has a mutation status of E449K, The gene ENO2 has a mutation status of P267S, The gene FAM186A has a mutation status of T1088N, The gene ESPL1 has a mutation status of W1776Ter, The gene NUAK1 has a mutation status of I417V, The gene HIP1R has a mutation status of H647Y, The gene ZNF605 has a mutation status of E621Ter, The gene ZMYM2 has a mutation status of L484WfsTer2, The gene GAS6 has a mutation status of Y258A, The gene CILP has a mutation status of R1176T, The gene BTBD1 has a mutation status of D231HfsTer33, The gene RCCD1 has a mutation status of P109Q, The gene PIGQ has a mutation status of R425Q, The gene GLOD4 has a mutation status of A281D, The gene MRM3 has a mutation status of V339N, The gene B4GALT6 has a mutation status of A39V, The gene MUC16 has a mutation status of S3959I, The gene TYK2 has a mutation status of A567P, The gene ZNF763 has a mutation status of V209F, The gene ZNF791 has a mutation status of E217K, The gene TM6SF2 has a mutation status of A263S, The gene SNRPA has a mutation status of I277F, The gene GSK3A has a mutation status of S2I, The gene ZNF541 has a mutation status of A607D, The gene C2orf16 has a mutation status of E1474D, The gene ADRA2B has a mutation status of S180F, The gene KANSL3 has a mutation status of R873L, The gene MFF has a mutation status of V148PfsTer27, The gene SCYGR7 has a mutation status of C94Ter, The gene SSTR4 has a mutation status of A245E, The gene BCAS1 has a mutation status of F96L, The gene TRMT2A has a mutation status of H601TfsTer36, The gene PPM1F has a mutation status of G273E, The gene OSBP2 has a mutation status of S42P, The gene BAP1 has a mutation status of A95D, The gene SLC25A36 has a mutation status of V89G, The gene MUC4 has a mutation status of L1410H, The gene SEC24B has a mutation status of A440V, The gene PCDHB6 has a mutation status of E203D, The gene PCDHGA7 has a mutation status of G571D, The gene SLC36A2 has a mutation status of A137V, The gene PHYKPL has a mutation status of P404A, The gene F13A1 has a mutation status of P28H, The gene FAM8A1 has a mutation status of A2D, The gene MRS2 has a mutation status of M383V, The gene TRIM15 has a mutation status of A368D, The gene HLA-C has a mutation status of Q204K, The gene VEGFA has a mutation status of M300V, The gene OPN5 has a mutation status of W188R, The gene FILIP1 has a mutation status of L1181RfsTer13, The gene PDE10A has a mutation status of R247S, The gene EIF3B has a mutation status of P151R, The gene POT1 has a mutation status of M159V, The gene TMEM178B has a mutation status of G205W, The gene CSMD1 has a mutation status of N2132K, The gene PLEC has a mutation status of E573K, The gene FOXE1 has a mutation status of A179S, The gene CYLC2 has a mutation status of M1?, The gene RC3H2 has a mutation status of P344L, The gene MAPKAP1 has a mutation status of D178N, The gene SURF4 has a mutation status of I225V, The gene MT-CYB has a mutation status of G351Ter, The gene FAM120C has a mutation status of E997NfsTer37, The gene ZMAT1 has a mutation status of F72G	KIPAN
The gene GLMN has a mutation status of R574Ter, The gene IGSF3 has a mutation status of R290Q, The gene TARS2 has a mutation status of G175V, The gene TDRKH has a mutation status of A404F, The gene ARHGEF11 has a mutation status of I1096L, The gene ATP1A4 has a mutation status of G737A, The gene NAV1 has a mutation status of S1335F, The gene CHI3L1 has a mutation status of W71C, The gene ARHGAP21 has a mutation status of P1252LfsTer2, The gene FGFBP3 has a mutation status of N172T, The gene INPP5F has a mutation status of P1057T, The gene MADD has a mutation status of D1148E, The gene DAGLA has a mutation status of Q284H, The gene ALG8 has a mutation status of H200R, The gene TENM4 has a mutation status of Q2708Ter, The gene GUCY1A2 has a mutation status of K717N, The gene KRAS has a mutation status of G12D, The gene AQP6 has a mutation status of G260E, The gene RIMBP2 has a mutation status of R1107W, The gene GOLGA3 has a mutation status of E790K, The gene PROSER1 has a mutation status of F806V, The gene KLF5 has a mutation status of H389N, The gene FRMD6 has a mutation status of T406I, The gene BTBD7 has a mutation status of S979R, The gene UNC13C has a mutation status of A1885T, The gene CILP has a mutation status of L1172R, The gene ADAMTS7 has a mutation status of T1662S, The gene NTRK3 has a mutation status of E322K, The gene PPL has a mutation status of K610T, The gene TMEM114 has a mutation status of I158R, The gene ABCC12 has a mutation status of D1113N, The gene MMP15 has a mutation status of F430V, The gene SYCE1L has a mutation status of D50E, The gene ZNF469 has a mutation status of S242I, The gene MYBBP1A has a mutation status of E758D, The gene CFAP52 has a mutation status of I487V, The gene CCT6B has a mutation status of V477L, The gene TSPOAP1 has a mutation status of L1102F, The gene RNFT1 has a mutation status of G316C, The gene ANKRD62 has a mutation status of S532L, The gene HCN2 has a mutation status of E154A, The gene PTPRS has a mutation status of Q1110Ter, The gene CATSPERD has a mutation status of T354I, The gene S1PR5 has a mutation status of L272V, The gene ZNF440 has a mutation status of E525V, The gene GTPBP3 has a mutation status of I64S, The gene ZNF91 has a mutation status of H960Y, The gene LILRA1 has a mutation status of P271R, The gene NLRP13 has a mutation status of E917K, The gene C2orf16 has a mutation status of E3942A, The gene PLEKHH2 has a mutation status of S329C, The gene NRXN1 has a mutation status of M690V, The gene CCDC85A has a mutation status of C18W, The gene MERTK has a mutation status of G787D, The gene XIRP2 has a mutation status of P1810S, The gene PRKRA has a mutation status of T204AfsTer22, The gene TTN has a mutation status of P29261T, The gene SLC39A10 has a mutation status of N150K, The gene SF3B1 has a mutation status of Q699_K700delinsHE, The gene PLCB4 has a mutation status of R254Q, The gene ZNF341 has a mutation status of A852S, The gene NCAM2 has a mutation status of I183R, The gene PCNT has a mutation status of E2293K, The gene SLC25A1 has a mutation status of N258T, The gene ZDHHC8 has a mutation status of N239T, The gene TRIOBP has a mutation status of E2097G, The gene CERK has a mutation status of L14R, The gene SHANK3 has a mutation status of K883Q, The gene PLCL2 has a mutation status of K25Q, The gene CDC25A has a mutation status of R506W, The gene BSN has a mutation status of E3469D, The gene TLR9 has a mutation status of Ter1033EextTer2, The gene DCBLD2 has a mutation status of E646K, The gene CD86 has a mutation status of S87IfsTer9, The gene PARP9 has a mutation status of P767S, The gene PLXNA1 has a mutation status of N466Y, The gene MUC4 has a mutation status of D2979_P3010del, The gene CPZ has a mutation status of Y269C, The gene PCDH7 has a mutation status of N212T, The gene ZFP2 has a mutation status of R122S, The gene FOXC1 has a mutation status of I313L, The gene TXNDC5 has a mutation status of T67A, The gene H1-3 has a mutation status of A29T, The gene ZSCAN12 has a mutation status of R398H, The gene OR10C1 has a mutation status of R233C, The gene COL11A2 has a mutation status of G826A, The gene DST has a mutation status of D6867V, The gene KCNQ5 has a mutation status of L32W, The gene COL12A1 has a mutation status of D1829N, The gene MFSD4B has a mutation status of L182Y, The gene TNFAIP3 has a mutation status of G156V, The gene SDK1 has a mutation status of K75Q, The gene GTF2I has a mutation status of S860Ter, The gene NPTX2 has a mutation status of L302VfsTer4, The gene PPP1R3A has a mutation status of T286S, The gene TRBV4-1 has a mutation status of K60R, The gene PRSS1 has a mutation status of C139S, The gene ZNF467 has a mutation status of E42D, The gene ATP6V0E2 has a mutation status of K30T, The gene REPIN1 has a mutation status of A296V, The gene KMT2C has a mutation status of D2201H, The gene KMT2C has a mutation status of D2024H, The gene KMT2C has a mutation status of G2002E, The gene KMT2C has a mutation status of M1938I, The gene KAT6A has a mutation status of R26C, The gene PPDPFL has a mutation status of S24P, The gene TCEA1 has a mutation status of I215L, The gene GABBR2 has a mutation status of V317M, The gene SMC2 has a mutation status of S342Ter, The gene ARPC5L has a mutation status of N21T, The gene MT-CYB has a mutation status of A380P, The gene ZXDA has a mutation status of D52E, The gene ZMAT1 has a mutation status of P10L, The gene LAGE3 has a mutation status of R114H	PAAD
The gene FAM131C has a mutation status of S203T, The gene CROCC has a mutation status of Q1245H, The gene CROCC has a mutation status of E1959Ter, The gene ACTL8 has a mutation status of R156H, The gene HSPG2 has a mutation status of T3344P, The gene OPRD1 has a mutation status of R146L, The gene LRRC8B has a mutation status of W116Ter, The gene TBX15 has a mutation status of S43Y, The gene SCNM1 has a mutation status of R206Q, The gene USP21 has a mutation status of L9V, The gene SPATA46 has a mutation status of A229V, The gene RGSL1 has a mutation status of H759C, The gene LAMC1 has a mutation status of A30G, The gene IGFN1 has a mutation status of P11S, The gene PCNX2 has a mutation status of R1122Ter, The gene MAP1LC3C has a mutation status of K6E, The gene ANKRD26 has a mutation status of E1466Q, The gene ATOH7 has a mutation status of F143L, The gene ECD has a mutation status of S534F, The gene DEAF1 has a mutation status of S48T, The gene PNPLA2 has a mutation status of T349P, The gene OSBPL5 has a mutation status of C273W, The gene TP53I11 has a mutation status of T101P, The gene F2 has a mutation status of Q387Ter, The gene KRAS has a mutation status of G12D, The gene SLC4A8 has a mutation status of L532P, The gene ITGB7 has a mutation status of S614G, The gene CMKLR1 has a mutation status of S13R, The gene SFSWAP has a mutation status of E428Q, The gene POLE has a mutation status of L690V, The gene COG3 has a mutation status of V43G, The gene RASA3 has a mutation status of E638Ter, The gene OR4Q3 has a mutation status of L113I, The gene NKX2-8 has a mutation status of A157V, The gene RTF1 has a mutation status of N699S, The gene SPPL2A has a mutation status of A200L, The gene TEX9 has a mutation status of T27I, The gene RASL12 has a mutation status of L53F, The gene COMMD4 has a mutation status of V37G, The gene C15orf40 has a mutation status of L2M, The gene EME2 has a mutation status of A253GfsTer57, The gene CLEC16A has a mutation status of P787L, The gene FHOD1 has a mutation status of E5G, The gene PLA2G15 has a mutation status of D56E, The gene FOXC2 has a mutation status of R165Q, The gene TP53 has a mutation status of P151S, The gene TMEM88 has a mutation status of Y110S, The gene GUCY2D has a mutation status of F355L, The gene RNF43 has a mutation status of E174Ter, The gene SEPTIN4 has a mutation status of R333C, The gene GNA13 has a mutation status of N215KfsTer8, The gene CCBE1 has a mutation status of F335L, The gene FBXO15 has a mutation status of I81M, The gene NFIC has a mutation status of P447R, The gene PEX11G has a mutation status of E12Ter, The gene JUND has a mutation status of E291D, The gene ZNF208 has a mutation status of N435K, The gene LILRB3 has a mutation status of V574A, The gene KIR2DL1 has a mutation status of S205A, The gene BIRC6 has a mutation status of E4123G, The gene TET3 has a mutation status of G153R, The gene LRRTM4 has a mutation status of M12V, The gene ITPRIPL1 has a mutation status of T228S, The gene NPHP1 has a mutation status of G534A, The gene MBD5 has a mutation status of L1449S, The gene SCN9A has a mutation status of E1865Q, The gene HOXD1 has a mutation status of S130A, The gene TTN has a mutation status of E35516K, The gene HSPE1 has a mutation status of M1?, The gene UNC80 has a mutation status of E55K, The gene PNKD has a mutation status of E295G, The gene TNFRSF6B has a mutation status of Q51P, The gene ZBTB46 has a mutation status of S110R, The gene COL18A1 has a mutation status of P187L, The gene MPST has a mutation status of S203P, The gene KLHL40 has a mutation status of G471AfsTer7, The gene GASK1A has a mutation status of A348P, The gene APEH has a mutation status of P320L, The gene ERC2 has a mutation status of A724V, The gene PDZRN3 has a mutation status of R156H, The gene CNTN3 has a mutation status of D530G, The gene KALRN has a mutation status of K1926M, The gene GPR149 has a mutation status of R310H, The gene CCDC39 has a mutation status of N849K, The gene LIPH has a mutation status of G77E, The gene DGKG has a mutation status of M422T, The gene MUC4 has a mutation status of A4086T, The gene TNK2 has a mutation status of E778D, The gene PACRGL has a mutation status of S59I, The gene RNF150 has a mutation status of V382I, The gene SFRP2 has a mutation status of R124Q, The gene SPEF2 has a mutation status of D707Y, The gene SELENOP has a mutation status of L269YfsTer?, The gene CCNO has a mutation status of T3P, The gene ERBIN has a mutation status of K455Q, The gene MAST4 has a mutation status of Q1884Ter, The gene SLF1 has a mutation status of H601Y, The gene SLC35A4 has a mutation status of L36W, The gene PCDHA6 has a mutation status of A484V, The gene GRIA1 has a mutation status of H566Q, The gene RNF44 has a mutation status of G354A, The gene ZFP2 has a mutation status of T39P, The gene DEK has a mutation status of A7T, The gene HLA-DQB1 has a mutation status of P84E, The gene ADGRF5 has a mutation status of T705A, The gene COL19A1 has a mutation status of G525C, The gene LAMA4 has a mutation status of H380Y, The gene FAM162B has a mutation status of G20V, The gene SCAF8 has a mutation status of V1254D, The gene URGCP has a mutation status of E550Q, The gene POLM has a mutation status of S425G, The gene ZNF804B has a mutation status of K489N, The gene PEG10 has a mutation status of S100L, The gene IQUB has a mutation status of E436G, The gene EPHA1 has a mutation status of D866A, The gene ZNF746 has a mutation status of E206D, The gene PXDNL has a mutation status of G732S, The gene GPR20 has a mutation status of G232S, The gene RANBP6 has a mutation status of L651F, The gene CDKN2A has a mutation status of R29_A34del, The gene TGFBR1 has a mutation status of N338S, The gene SVEP1 has a mutation status of V3422A, The gene LHX2 has a mutation status of H168R, The gene BARHL1 has a mutation status of Q304R, The gene SLC2A6 has a mutation status of C152Y, The gene ABCA2 has a mutation status of V1539G, The gene MT-ND4 has a mutation status of W359R, The gene USP9X has a mutation status of E264Q, The gene FOXP3 has a mutation status of W26C, The gene CENPVL3 has a mutation status of F106L, The gene DIAPH2 has a mutation status of L237P	PAAD
The gene COL16A1 has a mutation status of P249T, The gene A3GALT2 has a mutation status of A131T, The gene DOCK7 has a mutation status of R494K, The gene SSX2IP has a mutation status of H213Y, The gene ZNF326 has a mutation status of I384K, The gene ZNF326 has a mutation status of I385_E386delinsKK, The gene BRDT has a mutation status of N72TfsTer5, The gene AMIGO1 has a mutation status of R84C, The gene KCNC4 has a mutation status of R368H, The gene LMNA has a mutation status of I63L, The gene TOR1AIP1 has a mutation status of H479Y, The gene CAMK1G has a mutation status of S31L, The gene KIF26B has a mutation status of D165G, The gene PFKP has a mutation status of P421L, The gene RSF1 has a mutation status of P712S, The gene CLEC2D has a mutation status of G140D, The gene ATF7IP has a mutation status of L985TfsTer110, The gene PPP1R12A has a mutation status of R825KfsTer10, The gene CFAP54 has a mutation status of M1234CfsTer31, The gene CHD8 has a mutation status of N1040TfsTer12, The gene RABGGTA has a mutation status of A87S, The gene TTC6 has a mutation status of E252D, The gene ASB7 has a mutation status of G80R, The gene NDUFB10 has a mutation status of K152E, The gene GPS2 has a mutation status of K54RfsTer9, The gene NLGN2 has a mutation status of F812L, The gene GJD3 has a mutation status of H175Y, The gene NAGS has a mutation status of N294D, The gene ARHGAP27 has a mutation status of K673E, The gene MEP1B has a mutation status of T214LfsTer21, The gene ZNF729 has a mutation status of C908S, The gene ZNF536 has a mutation status of R381C, The gene ERF has a mutation status of G299EfsTer12, The gene PPP5C has a mutation status of R16GfsTer10, The gene DACT3 has a mutation status of L79P, The gene CTU1 has a mutation status of S269L, The gene ZNF610 has a mutation status of H366R, The gene ZNF880 has a mutation status of N139_N140insD, The gene ZNF415 has a mutation status of V11L, The gene ADGRF3 has a mutation status of Q55R, The gene ACVR1 has a mutation status of W245Ter, The gene TTN has a mutation status of A35263F, The gene ANKAR has a mutation status of G458Ter, The gene WNT6 has a mutation status of Q238Ter, The gene RALGAPA2 has a mutation status of Q565P, The gene EFCAB8 has a mutation status of L525M, The gene DGCR2 has a mutation status of G194V, The gene ANKRD54 has a mutation status of R201VfsTer2, The gene SREBF2 has a mutation status of L212P, The gene ZBED4 has a mutation status of A839T, The gene SETD2 has a mutation status of G2263RfsTer9, The gene IP6K2 has a mutation status of H386Y, The gene CNTN3 has a mutation status of V359A, The gene ABI3BP has a mutation status of A1544V, The gene ZBTB20 has a mutation status of P692LfsTer43, The gene ATR has a mutation status of S1038LfsTer12, The gene MUC4 has a mutation status of G3980VfsTer279, The gene MUC4 has a mutation status of D2979_P3010del, The gene ZFYVE28 has a mutation status of H261L, The gene HTT has a mutation status of A274T, The gene ELF2 has a mutation status of M171K, The gene TNXB has a mutation status of S3077G, The gene SLC22A16 has a mutation status of C148_D149delinsTer, The gene RWDD1 has a mutation status of Q128K, The gene PSMG3 has a mutation status of R113M, The gene NFE2L3 has a mutation status of S422del, The gene ZNF394 has a mutation status of E522K, The gene FUT10 has a mutation status of L418V, The gene ADAM18 has a mutation status of P391R, The gene POTEA has a mutation status of V558_A559del, The gene THEM6 has a mutation status of A90RfsTer2, The gene ZFP37 has a mutation status of C519Y, The gene CDK9 has a mutation status of P197RfsTer79, The gene MT-ND6 has a mutation status of T159M, The gene HMGN5 has a mutation status of E276RfsTer18	GBMLGG
The gene CFAP74 has a mutation status of T583P, The gene RFX5 has a mutation status of R335P, The gene CD5L has a mutation status of K154N, The gene ASTN1 has a mutation status of Y803C, The gene STIP1 has a mutation status of E208K, The gene PCNX3 has a mutation status of H1434P, The gene MUC19 has a mutation status of R4518_D4519delinsSH, The gene ENDOU has a mutation status of T88P, The gene NTS has a mutation status of E27Ter, The gene ITGBL1 has a mutation status of D148E, The gene SERPINA1 has a mutation status of N53K, The gene TJP1 has a mutation status of A1494S, The gene PRTG has a mutation status of S267Y, The gene TMEM266 has a mutation status of I166V, The gene PDZD9 has a mutation status of Q104K, The gene TUFM has a mutation status of E193DfsTer19, The gene LOXHD1 has a mutation status of V2234G, The gene REXO1 has a mutation status of H665P, The gene ZNF257 has a mutation status of C126H, The gene ZNF257 has a mutation status of G128Q, The gene ZNF382 has a mutation status of N534D, The gene LILRA4 has a mutation status of R399Y, The gene EN1 has a mutation status of A163E, The gene TTN has a mutation status of A6097S, The gene ACSS1 has a mutation status of V431G, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene ANKRD28 has a mutation status of H76Y, The gene TRIM71 has a mutation status of N545D, The gene DNAH5 has a mutation status of E1926Q, The gene MCTP1 has a mutation status of Y261Ter, The gene PCDHB10 has a mutation status of S774Ter, The gene OR10C1 has a mutation status of T64P, The gene HLA-C has a mutation status of T187L, The gene AKAP9 has a mutation status of R2607G, The gene MUC3A has a mutation status of W18G, The gene HR has a mutation status of N232K, The gene LAPTM4B has a mutation status of M88K, The gene HAS2 has a mutation status of E224D, The gene MT-CYB has a mutation status of M124V, The gene ARSF has a mutation status of R386L, The gene SCML1 has a mutation status of L119I, The gene DCAF12L2 has a mutation status of V237G, The gene DDX3Y has a mutation status of C221F	KIPAN
The gene ATAD3C has a mutation status of E30Ter, The gene PLCH2 has a mutation status of T389SfsTer9, The gene CA6 has a mutation status of H141Y, The gene SRRM1 has a mutation status of T274_K283del, The gene LRRIQ3 has a mutation status of I577R, The gene GBP1 has a mutation status of E147Ter, The gene ASH1L has a mutation status of E515K, The gene CD1C has a mutation status of D106N, The gene IFI16 has a mutation status of F440L, The gene CEP350 has a mutation status of D1901Y, The gene HMCN1 has a mutation status of R325G, The gene KCNT2 has a mutation status of R346K, The gene RYR2 has a mutation status of D1298N, The gene RYR2 has a mutation status of E2769K, The gene OR2T6 has a mutation status of V213A, The gene TIMM23 has a mutation status of S208L, The gene NCOA4 has a mutation status of N393K, The gene PTEN has a mutation status of L108R, The gene GPAM has a mutation status of P681L, The gene PNLIPRP3 has a mutation status of N136S, The gene WDR11 has a mutation status of K155RfsTer20, The gene PKP3 has a mutation status of D595V, The gene HRAS has a mutation status of E162K, The gene MUC6 has a mutation status of Q1821_T1822delinsHA, The gene MEN1 has a mutation status of I457Ter, The gene KLC2 has a mutation status of E215K, The gene CD248 has a mutation status of R225L, The gene EXPH5 has a mutation status of S127F, The gene CACNA1C has a mutation status of R1187Ter, The gene GPR19 has a mutation status of R258Q, The gene MUC19 has a mutation status of R6489T, The gene RIMBP2 has a mutation status of G1246WfsTer2, The gene TMTC4 has a mutation status of R750K, The gene ADPRHL1 has a mutation status of E1726G, The gene ADPRHL1 has a mutation status of S686L, The gene DCUN1D2 has a mutation status of F259L, The gene SALL2 has a mutation status of A897V, The gene TNFAIP2 has a mutation status of R645W, The gene HERC2 has a mutation status of T1472M, The gene DUOX1 has a mutation status of E271K, The gene DTWD1 has a mutation status of D296G, The gene C2CD4B has a mutation status of A219S, The gene ACAN has a mutation status of D200G, The gene SYNGR3 has a mutation status of F40L, The gene PYDC1 has a mutation status of V30M, The gene CDH8 has a mutation status of P424T, The gene DDX19A has a mutation status of G395S, The gene ANKRD11 has a mutation status of D1261H, The gene ANKRD11 has a mutation status of E1203Q, The gene RNF135 has a mutation status of R56P, The gene THRA has a mutation status of E343K, The gene KRT24 has a mutation status of V73G, The gene KIF18B has a mutation status of C782Y, The gene OSBPL7 has a mutation status of M46I, The gene TNRC6C has a mutation status of G1124E, The gene SLC16A3 has a mutation status of H350Q, The gene L3MBTL4 has a mutation status of D234N, The gene L3MBTL4 has a mutation status of K167_A168del, The gene L3MBTL4 has a mutation status of L166F, The gene LAMA1 has a mutation status of Q3027K, The gene ZNF521 has a mutation status of D880E, The gene SLC25A52 has a mutation status of K9N, The gene DTNA has a mutation status of R337S, The gene TSHZ1 has a mutation status of E1073K, The gene TUBB4A has a mutation status of R359C, The gene ZNF99 has a mutation status of G207C, The gene ZNF724 has a mutation status of E503D, The gene ZNF181 has a mutation status of H427Y, The gene KMT2B has a mutation status of R2712Q, The gene ZNF607 has a mutation status of H639Y, The gene SPTBN4 has a mutation status of Q2046H, The gene SPTBN4 has a mutation status of E2082K, The gene SPTBN4 has a mutation status of E2154Q, The gene KCNC3 has a mutation status of D225N, The gene SIGLEC10 has a mutation status of P311R, The gene MZF1 has a mutation status of L24I, The gene MYT1L has a mutation status of R924W, The gene ANKRD36 has a mutation status of R405S, The gene TSN has a mutation status of R182H, The gene WDR33 has a mutation status of R974W, The gene ABCB11 has a mutation status of A75T, The gene PDE11A has a mutation status of F257L, The gene IKZF2 has a mutation status of Q144K, The gene VIL1 has a mutation status of Q323Ter, The gene VIL1 has a mutation status of Q343Ter, The gene DOCK10 has a mutation status of E1679K, The gene ANKRD60 has a mutation status of C190F, The gene LAMA5 has a mutation status of P1458S, The gene TPTE has a mutation status of T347I, The gene GAB4 has a mutation status of R92C, The gene SYNPR has a mutation status of S176L, The gene MAGI1 has a mutation status of R1405G, The gene MAGI1 has a mutation status of D1168G, The gene CLDND1 has a mutation status of E61K, The gene MYLK has a mutation status of E1414K, The gene ARHGEF26 has a mutation status of K466N, The gene KLHL6 has a mutation status of V541G, The gene MUC4 has a mutation status of T3942L, The gene CRACD has a mutation status of T1148S, The gene UGT2B28 has a mutation status of F119_H120delinsLY, The gene ZGRF1 has a mutation status of F116S, The gene SPATA5 has a mutation status of F219LfsTer17, The gene SLC7A11 has a mutation status of E348K, The gene IQCM has a mutation status of S60F, The gene DCLK2 has a mutation status of R414K, The gene ASIC5 has a mutation status of H212R, The gene SELENOP has a mutation status of C140Y, The gene FAT2 has a mutation status of R3465Ter, The gene H2AC14 has a mutation status of A41G, The gene TTBK1 has a mutation status of P457L, The gene CILK1 has a mutation status of S626F, The gene ARMC2 has a mutation status of C353Ter, The gene AFDN has a mutation status of R1648Ter, The gene AFDN has a mutation status of K1650RfsTer3, The gene SUN1 has a mutation status of P573S, The gene FOXK1 has a mutation status of T683A, The gene OSBPL3 has a mutation status of L835Q, The gene TAX1BP1 has a mutation status of N294K, The gene TAX1BP1 has a mutation status of T295S, The gene CAMK2B has a mutation status of Q624E, The gene FIGNL1 has a mutation status of W666Ter, The gene MUC3A has a mutation status of W18G, The gene WNT2 has a mutation status of R183T, The gene CALD1 has a mutation status of E186Ter, The gene TAS2R3 has a mutation status of R55S, The gene ZNF862 has a mutation status of L248P, The gene PTPRN2 has a mutation status of E42K, The gene ERI1 has a mutation status of E282Q, The gene SCARA5 has a mutation status of G318V, The gene FUT10 has a mutation status of A102V, The gene TRIQK has a mutation status of E85K, The gene VPS13B has a mutation status of E2370K, The gene NCALD has a mutation status of P139L, The gene TG has a mutation status of R995H, The gene C8orf82 has a mutation status of G6V, The gene KLF9 has a mutation status of Y164F, The gene ZNF462 has a mutation status of D686Y, The gene MIGA2 has a mutation status of Q179E, The gene WDR5 has a mutation status of E58K, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene FAM47C has a mutation status of S842F, The gene OTC has a mutation status of L42F, The gene TEX13C has a mutation status of G11E, The gene CXorf66 has a mutation status of D326Y, The gene MAGEC1 has a mutation status of D123E, The gene PASD1 has a mutation status of E202K, The gene LRRC47 has a mutation status of G119C, The gene CA6 has a mutation status of H141Y, The gene UBR4 has a mutation status of A684Ter, The gene HSPG2 has a mutation status of G1243W, The gene HPCA has a mutation status of F193L, The gene CSMD2 has a mutation status of F2196V, The gene LRRIQ3 has a mutation status of I577R, The gene GBP1 has a mutation status of E147Ter, The gene MSTO1 has a mutation status of W535L, The gene DAP3 has a mutation status of A33T, The gene CD1C has a mutation status of D106N, The gene AIM2 has a mutation status of D199N, The gene HMCN1 has a mutation status of R325G, The gene ZBTB41 has a mutation status of C639Y, The gene FCMR has a mutation status of A327S, The gene FCMR has a mutation status of G324V, The gene COQ8A has a mutation status of K358N, The gene RYR2 has a mutation status of D1298N, The gene RYR2 has a mutation status of E2769K, The gene FMN2 has a mutation status of A260G, The gene FMN2 has a mutation status of E262G, The gene PITRM1 has a mutation status of V12L, The gene TYSND1 has a mutation status of V37G, The gene PTEN has a mutation status of L108R, The gene C10orf95 has a mutation status of Y152S, The gene SMC3 has a mutation status of T1094I, The gene GPAM has a mutation status of P681L, The gene WDR11 has a mutation status of K155RfsTer20, The gene HRAS has a mutation status of E162K, The gene MUC5AC has a mutation status of P3819T, The gene PRR33 has a mutation status of P439T, The gene PRR33 has a mutation status of E305Q, The gene OTOG has a mutation status of P1523S, The gene OR4S1 has a mutation status of L152M, The gene MEN1 has a mutation status of I457Ter, The gene KLC2 has a mutation status of E215K, The gene UNC93B1 has a mutation status of M1?, The gene CREBZF has a mutation status of E249D, The gene HEPHL1 has a mutation status of L1125F, The gene PGR has a mutation status of E466K, The gene EXPH5 has a mutation status of S127F, The gene TECTA has a mutation status of S2051F, The gene CACNA1C has a mutation status of R1187Ter, The gene TAS2R43 has a mutation status of H93RfsTer35, The gene RESF1 has a mutation status of I1671M, The gene KMT2D has a mutation status of Q3860H, The gene HOXC13 has a mutation status of A237P, The gene NFE2 has a mutation status of P216A, The gene CHPT1 has a mutation status of V39G, The gene HSP90B1 has a mutation status of I66M, The gene RFLNA has a mutation status of T182P, The gene RIMBP2 has a mutation status of G1246WfsTer2, The gene TMTC4 has a mutation status of R750K, The gene DCUN1D2 has a mutation status of F259L, The gene TNFAIP2 has a mutation status of R645W, The gene JAG2 has a mutation status of G725V, The gene HERC2 has a mutation status of T1472M, The gene DTWD1 has a mutation status of D296G, The gene ACAN has a mutation status of D200G, The gene MCRIP2 has a mutation status of A13E, The gene ANTKMT has a mutation status of A39G, The gene NTN3 has a mutation status of P37T, The gene STX1B has a mutation status of N161S, The gene PYDC1 has a mutation status of V30M, The gene CDH8 has a mutation status of P424T, The gene DDX19A has a mutation status of G395S, The gene ANKRD11 has a mutation status of D1261H, The gene ANKRD11 has a mutation status of E1203Q, The gene MINK1 has a mutation status of A520D, The gene NOS2 has a mutation status of E145K, The gene THRA has a mutation status of E343K, The gene RAPGEFL1 has a mutation status of L8M, The gene RAMP2 has a mutation status of V6_R26del, The gene KIF18B has a mutation status of C782Y, The gene CHCT1 has a mutation status of K13N, The gene ABCA8 has a mutation status of V78I, The gene PRPSAP1 has a mutation status of P20T, The gene TNRC6C has a mutation status of G1124E, The gene CANT1 has a mutation status of E284D, The gene LRRC45 has a mutation status of R602L, The gene SLC16A3 has a mutation status of H350Q, The gene L3MBTL4 has a mutation status of D234N, The gene L3MBTL4 has a mutation status of K167_A168del, The gene L3MBTL4 has a mutation status of L166F, The gene ZNF521 has a mutation status of D880E, The gene SLC25A52 has a mutation status of K9N, The gene DTNA has a mutation status of R337S, The gene TSHZ1 has a mutation status of E1073K, The gene SHC2 has a mutation status of H141P, The gene GPX4 has a mutation status of G17A, The gene MKNK2 has a mutation status of Y256D, The gene LINGO3 has a mutation status of E55Ter, The gene MFSD12 has a mutation status of V197G, The gene TUBB4A has a mutation status of R359C, The gene PKN1 has a mutation status of T302P, The gene WIZ has a mutation status of I1673L, The gene ANO8 has a mutation status of A31S, The gene ZNF99 has a mutation status of G207C, The gene ZNF724 has a mutation status of E503D, The gene ZNF181 has a mutation status of H427Y, The gene KMT2B has a mutation status of R2712Q, The gene ZNF607 has a mutation status of H639Y, The gene PAK4 has a mutation status of S134R, The gene SPTBN4 has a mutation status of A1492G, The gene SPTBN4 has a mutation status of Q2046H, The gene SPTBN4 has a mutation status of E2154Q, The gene DEDD2 has a mutation status of E316G, The gene PPP1R37 has a mutation status of P631T, The gene DACT3 has a mutation status of Q49H, The gene PRR12 has a mutation status of P778T, The gene KCNC3 has a mutation status of D225N, The gene SPACA6 has a mutation status of A9T, The gene MBOAT7 has a mutation status of A267S, The gene ZNF787 has a mutation status of I235L, The gene MYT1L has a mutation status of R924W, The gene GCKR has a mutation status of G607V, The gene CAPN14 has a mutation status of W317C, The gene WDR33 has a mutation status of R974W, The gene GRB14 has a mutation status of G59V, The gene ABCB11 has a mutation status of A75T, The gene IKZF2 has a mutation status of Q144K, The gene IGFBP2 has a mutation status of V38G, The gene VIL1 has a mutation status of Q323Ter, The gene VIL1 has a mutation status of Q343Ter, The gene CHPF has a mutation status of A542S, The gene DOCK10 has a mutation status of E1679K, The gene CROCC2 has a mutation status of A529E, The gene ATG4B has a mutation status of S68Ter, The gene ANKRD60 has a mutation status of C190F, The gene LAMA5 has a mutation status of P1458S, The gene TPTE has a mutation status of T347I, The gene RCAN1 has a mutation status of G7V, The gene RCAN1 has a mutation status of A6S, The gene RSPH1 has a mutation status of N165K, The gene YBEY has a mutation status of P158S, The gene GAB4 has a mutation status of R92C, The gene THAP7 has a mutation status of R21L, The gene APOBEC3F has a mutation status of H4N, The gene ADSL has a mutation status of A47GfsTer14, The gene CSDC2 has a mutation status of S16Y, The gene CSDC2 has a mutation status of P17H, The gene PARVB has a mutation status of P12T, The gene SBF1 has a mutation status of D202Y, The gene CHKB has a mutation status of E96Ter, The gene VIPR1 has a mutation status of A9D, The gene GASK1A has a mutation status of S295Y, The gene ITIH4 has a mutation status of P676S, The gene ARHGEF3 has a mutation status of F413L, The gene SYNPR has a mutation status of S176L, The gene MAGI1 has a mutation status of R1405G, The gene MAGI1 has a mutation status of D1168G, The gene CLDND1 has a mutation status of E61K, The gene CCDC54 has a mutation status of L136I, The gene MYLK has a mutation status of E1414K, The gene PLOD2 has a mutation status of V302F, The gene ARHGEF26 has a mutation status of K466N, The gene KLHL6 has a mutation status of V541G, The gene MUC4 has a mutation status of D3957RfsTer66, The gene BEND4 has a mutation status of N255K, The gene CRACD has a mutation status of T1148S, The gene UBA6 has a mutation status of S650F, The gene UGT2B28 has a mutation status of F119_H120delinsLY, The gene ZGRF1 has a mutation status of F116S, The gene SPATA5 has a mutation status of F219LfsTer17, The gene SLC7A11 has a mutation status of E348K, The gene DCLK2 has a mutation status of R414K, The gene ASIC5 has a mutation status of H212R, The gene SDHA has a mutation status of V4G, The gene TRIP13 has a mutation status of G29S, The gene SELENOP has a mutation status of C140Y, The gene ADGRV1 has a mutation status of T1402S, The gene CAMLG has a mutation status of V16G, The gene PCDHGB3 has a mutation status of L604M, The gene FAT2 has a mutation status of R3465Ter, The gene PWWP2A has a mutation status of E24Ter, The gene CCNJL has a mutation status of T274P, The gene C5orf47 has a mutation status of R94L, The gene SLC22A23 has a mutation status of D117Y, The gene H2AC14 has a mutation status of A41G, The gene FKBPL has a mutation status of Ter350SextTer6, The gene DAAM2 has a mutation status of A196T, The gene TTBK1 has a mutation status of P457L, The gene RUNX2 has a mutation status of L392M, The gene AFDN has a mutation status of R1648Ter, The gene AFDN has a mutation status of K1650RfsTer3, The gene SUN1 has a mutation status of P573S, The gene ZNF853 has a mutation status of Q186K, The gene OSBPL3 has a mutation status of L835Q, The gene CAMK2B has a mutation status of Q624E, The gene FIGNL1 has a mutation status of W666Ter, The gene SLC12A9 has a mutation status of R825L, The gene SLC26A5 has a mutation status of E468Ter, The gene WNT2 has a mutation status of R183T, The gene PRRT4 has a mutation status of G466S, The gene CALD1 has a mutation status of E186Ter, The gene ZC3HAV1L has a mutation status of E98D, The gene TAS2R3 has a mutation status of R55S, The gene NOBOX has a mutation status of D401Y, The gene ZNF746 has a mutation status of Y443S, The gene ZNF862 has a mutation status of L248P, The gene ERI1 has a mutation status of E282Q, The gene TEX15 has a mutation status of D303G, The gene TRIQK has a mutation status of E85K, The gene VPS13B has a mutation status of E2370K, The gene NCALD has a mutation status of P139L, The gene EMC2 has a mutation status of S5L, The gene SQLE has a mutation status of D427IfsTer2, The gene TG has a mutation status of R995H, The gene ADGRB1 has a mutation status of Q325K, The gene EEF1D has a mutation status of Y239D, The gene FAM83H has a mutation status of A387S, The gene PLEC has a mutation status of F1796V, The gene C8orf82 has a mutation status of G6V, The gene FOCAD has a mutation status of G33V, The gene APBA1 has a mutation status of R143C, The gene KLF9 has a mutation status of Y164F, The gene GAS1 has a mutation status of V163G, The gene WNK2 has a mutation status of Y1923S, The gene ZNF462 has a mutation status of D686Y, The gene ODF2 has a mutation status of P27T, The gene MIGA2 has a mutation status of Q179E, The gene NTNG2 has a mutation status of S178P, The gene WDR5 has a mutation status of E58K, The gene MT-ND3 has a mutation status of S90T, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene SHROOM2 has a mutation status of D865A, The gene FAM47C has a mutation status of S842F, The gene OTC has a mutation status of L42F, The gene FOXP3 has a mutation status of G40V, The gene AR has a mutation status of A417E, The gene NHSL2 has a mutation status of T662K, The gene COL4A5 has a mutation status of G693R, The gene CXorf66 has a mutation status of D326Y, The gene MAGEC1 has a mutation status of D123E, The gene PASD1 has a mutation status of E202K	BRCA
The gene CLSTN1 has a mutation status of A13V, The gene CLSTN1 has a mutation status of A6T, The gene S100PBP has a mutation status of G185C, The gene SZT2 has a mutation status of D2384E, The gene ENSA has a mutation status of G68A, The gene NUP210L has a mutation status of Y1072H, The gene MGST3 has a mutation status of A133V, The gene KIFAP3 has a mutation status of V323A, The gene STX6 has a mutation status of R55Q, The gene ARL8A has a mutation status of V37I, The gene ARL8A has a mutation status of K33M, The gene LYST has a mutation status of M2742T, The gene PPRC1 has a mutation status of P962L, The gene PLEKHA7 has a mutation status of Y778C, The gene MADD has a mutation status of M1571T, The gene APLNR has a mutation status of S56N, The gene OR1S1 has a mutation status of L143F, The gene TNFRSF1A has a mutation status of Y236LfsTer19, The gene TNFRSF1A has a mutation status of R235HfsTer119, The gene SCNN1A has a mutation status of R181W, The gene ARHGDIB has a mutation status of V59M, The gene SLC2A13 has a mutation status of N142S, The gene LRRK2 has a mutation status of Q1365R, The gene MUC19 has a mutation status of P1322Q, The gene BLTP3B has a mutation status of Y734Ter, The gene DNAH10 has a mutation status of D72V, The gene MTRF1 has a mutation status of K138R, The gene DGKH has a mutation status of T697N, The gene TTC6 has a mutation status of E252D, The gene IRF2BPL has a mutation status of V76RfsTer50, The gene GALC has a mutation status of I102V, The gene MTMR10 has a mutation status of S27L, The gene TEKT5 has a mutation status of I303N, The gene RBBP6 has a mutation status of K1780EfsTer5, The gene ITGAD has a mutation status of Q325Ter, The gene CHST6 has a mutation status of R359Q, The gene ADAMTS18 has a mutation status of Q612Ter, The gene CPNE7 has a mutation status of V413L, The gene TP53 has a mutation status of L265P, The gene BRCA1 has a mutation status of H619N, The gene UBE2Z has a mutation status of M335_D336delinsIY, The gene USP32 has a mutation status of Y110C, The gene ABCA8 has a mutation status of K624R, The gene RNF152 has a mutation status of F16C, The gene MUC16 has a mutation status of G12642S, The gene SMARCA4 has a mutation status of E1499Ter, The gene ZNF681 has a mutation status of E628K, The gene TDRD12 has a mutation status of A958T, The gene GRAMD1A has a mutation status of D693N, The gene LILRA1 has a mutation status of P271R, The gene ZNF324 has a mutation status of L445F, The gene LRATD1 has a mutation status of A134V, The gene ZNF638 has a mutation status of Q459L, The gene IGKV1D-43 has a mutation status of A35E, The gene ANKRD36 has a mutation status of R405S, The gene POLR1B has a mutation status of D809E, The gene XIRP2 has a mutation status of K1553Ter, The gene XIRP2 has a mutation status of Y2551IfsTer2, The gene CFAP210 has a mutation status of A107V, The gene TTN has a mutation status of S3280P, The gene LBP has a mutation status of R254H, The gene LAMA5 has a mutation status of S1800L, The gene KRTAP19-5 has a mutation status of S57G, The gene SH3BGR has a mutation status of L97W, The gene TBC1D22A has a mutation status of T149A, The gene ZBED4 has a mutation status of Q774R, The gene DOCK3 has a mutation status of L278V, The gene MUC4 has a mutation status of T3942L, The gene MUC4 has a mutation status of D2979_P3010del, The gene MUC4 has a mutation status of T2491S, The gene EVC has a mutation status of A864D, The gene TBC1D1 has a mutation status of C178W, The gene KLB has a mutation status of A167D, The gene UGT2B17 has a mutation status of K287I, The gene UGT2B17 has a mutation status of K284I, The gene RAPGEF2 has a mutation status of E307G, The gene RAI14 has a mutation status of V821F, The gene PIK3R1 has a mutation status of Y463_D464insELHEYNTQFQEKSREY, The gene TMEM167A has a mutation status of T12S, The gene PCDHB12 has a mutation status of P674L, The gene SLIT3 has a mutation status of A21V, The gene MAML1 has a mutation status of A86T, The gene ATAT1 has a mutation status of S259P, The gene HLA-DRB5 has a mutation status of Y42H, The gene TRERF1 has a mutation status of Q1132K, The gene PTK7 has a mutation status of T635N, The gene DST has a mutation status of S4283IfsTer2, The gene AHI1 has a mutation status of S462P, The gene ARFGEF3 has a mutation status of N95S, The gene RADIL has a mutation status of R212H, The gene ZNF12 has a mutation status of E602D, The gene SEPTIN14 has a mutation status of G50R, The gene GUSB has a mutation status of R327C, The gene ZKSCAN5 has a mutation status of Q498K, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of N2136_E2152del, The gene TMEM168 has a mutation status of H642TfsTer30, The gene CADPS2 has a mutation status of A966S, The gene XPO7 has a mutation status of M740V, The gene DOCK5 has a mutation status of Y1388Ter, The gene NSD3 has a mutation status of F34LfsTer110, The gene NSD3 has a mutation status of D32LfsTer2, The gene PAG1 has a mutation status of L423F, The gene PTPRD has a mutation status of V1284D, The gene TMC1 has a mutation status of E517Q, The gene WNK2 has a mutation status of P1515S, The gene PSMB7 has a mutation status of S5L, The gene MT-CYB has a mutation status of S172N, The gene ARSH has a mutation status of A187D, The gene SLC7A3 has a mutation status of R529I, The gene INTS6L has a mutation status of M437I	GBMLGG
The gene FOXJ3 has a mutation status of S227I, The gene CYP4A22 has a mutation status of A124P, The gene NBPF12 has a mutation status of D1432E, The gene PRCC has a mutation status of K137E, The gene IGSF8 has a mutation status of E55K, The gene LY9 has a mutation status of E74DfsTer2, The gene DYRK3 has a mutation status of L311S, The gene USH2A has a mutation status of E4461K, The gene INPP5F has a mutation status of S793F, The gene FUOM has a mutation status of S12F, The gene KIAA1549L has a mutation status of L1855P, The gene OR4C15 has a mutation status of F101Ter, The gene OR8U1 has a mutation status of Y149H, The gene OR8U1 has a mutation status of M155V, The gene KDM4F has a mutation status of I49V, The gene SIAE has a mutation status of S252C, The gene C1S has a mutation status of E608K, The gene ABCC9 has a mutation status of T1053K, The gene KRT6C has a mutation status of I523L, The gene KMT5A has a mutation status of K98Q, The gene TRPM1 has a mutation status of M718PfsTer72, The gene ZNF280D has a mutation status of S112T, The gene MCTP2 has a mutation status of C449F, The gene CLCN7 has a mutation status of E732Ter, The gene CLCN7 has a mutation status of H725L, The gene ZNF213 has a mutation status of R132P, The gene CIITA has a mutation status of M210I, The gene MAPK3 has a mutation status of G102S, The gene ZNF48 has a mutation status of S66P, The gene BBS2 has a mutation status of D296G, The gene NFATC3 has a mutation status of S975L, The gene GCSH has a mutation status of M159L, The gene YBX2 has a mutation status of G340V, The gene THRA has a mutation status of K337R, The gene SEPTIN4 has a mutation status of P893S, The gene FBF1 has a mutation status of A919G, The gene CCDC40 has a mutation status of E804D, The gene DSG2 has a mutation status of E820Ter, The gene SALL3 has a mutation status of A245V, The gene C2CD4C has a mutation status of P157H, The gene PTBP1 has a mutation status of G123D, The gene ELANE has a mutation status of F218L, The gene ZNF561 has a mutation status of E394G, The gene SLC27A1 has a mutation status of E426K, The gene ZNF850 has a mutation status of F16C, The gene LILRB1 has a mutation status of Y99I, The gene GDF7 has a mutation status of L234M, The gene DNMT3A has a mutation status of C487Y, The gene ABHD1 has a mutation status of V43A, The gene XDH has a mutation status of S123G, The gene SPTBN1 has a mutation status of L240V, The gene ASTL has a mutation status of A49G, The gene TTN has a mutation status of M31425T, The gene FAM171B has a mutation status of G506V, The gene ANKAR has a mutation status of Y734S, The gene RBM44 has a mutation status of W381CfsTer3, The gene ADAM33 has a mutation status of R383C, The gene HMGB1P1 has a mutation status of H70R, The gene LAMA5 has a mutation status of V1602M, The gene DGCR8 has a mutation status of R262Q, The gene CACNA1I has a mutation status of H1042R, The gene SLC4A7 has a mutation status of E750G, The gene DOCK3 has a mutation status of I444F, The gene KALRN has a mutation status of I2815V, The gene RARRES1 has a mutation status of I191M, The gene ZBBX has a mutation status of A702S, The gene CCDC50 has a mutation status of R330S, The gene MAN2B2 has a mutation status of D38V, The gene RBPJ has a mutation status of P15L, The gene PCDH10 has a mutation status of G765S, The gene TMEM144 has a mutation status of A108E, The gene HMGCS1 has a mutation status of G3R, The gene ZNF184 has a mutation status of P473S, The gene HLA-DQB2 has a mutation status of V37Y, The gene RPS6KA2 has a mutation status of R722C, The gene HYCC1 has a mutation status of R510G, The gene COBL has a mutation status of G898R, The gene MUC3A has a mutation status of S326A, The gene MUC3A has a mutation status of T363M, The gene MUC3A has a mutation status of T433N, The gene PNPLA8 has a mutation status of G93Ter, The gene CTTNBP2 has a mutation status of I71S, The gene TAS2R60 has a mutation status of M85L, The gene SFRP1 has a mutation status of A254S, The gene SOX17 has a mutation status of V386E, The gene NIPAL2 has a mutation status of I340V, The gene FAM83A has a mutation status of Q370H, The gene PIGO has a mutation status of R664G, The gene SEC16A has a mutation status of S1193R, The gene MXRA5 has a mutation status of L2562F, The gene MAGIX has a mutation status of S80I, The gene ARMCX1 has a mutation status of G248C, The gene SLC25A5 has a mutation status of T221R	SARC
The gene SLC45A1 has a mutation status of T497A, The gene OTUD3 has a mutation status of Q97PfsTer15, The gene RLF has a mutation status of V1887A, The gene SPATA6 has a mutation status of T76A, The gene VCAM1 has a mutation status of K4NfsTer22, The gene KCNA3 has a mutation status of E262K, The gene CHIA has a mutation status of Y203C, The gene DENND2C has a mutation status of C675F, The gene VANGL1 has a mutation status of P498T, The gene TTF2 has a mutation status of T724HfsTer6, The gene MNDA has a mutation status of T244I, The gene ATP1A4 has a mutation status of H501P, The gene CACNA1S has a mutation status of F1187S, The gene USH2A has a mutation status of R4392I, The gene SFTPA1 has a mutation status of P62L, The gene DNTT has a mutation status of T169A, The gene HIPK3 has a mutation status of N1032S, The gene SPTBN2 has a mutation status of A1641V, The gene C11orf24 has a mutation status of H73R, The gene SHANK2 has a mutation status of E1283RfsTer17, The gene DYNC2H1 has a mutation status of F948LfsTer9, The gene APOA5 has a mutation status of S212R, The gene CD3G has a mutation status of S148L, The gene TAS2R9 has a mutation status of K110Q, The gene ADAMTS20 has a mutation status of A327D, The gene RAPGEF3 has a mutation status of G382D, The gene TAFA2 has a mutation status of V85G, The gene ZFC3H1 has a mutation status of A1913G, The gene PTPRQ has a mutation status of V537A, The gene CEP290 has a mutation status of E795K, The gene LTA4H has a mutation status of D258V, The gene HCFC2 has a mutation status of G496S, The gene DNAH10 has a mutation status of E523GfsTer22, The gene MRPL52 has a mutation status of S49Ter, The gene STRN3 has a mutation status of I417L, The gene PRIMA1 has a mutation status of V7CfsTer26, The gene BEGAIN has a mutation status of G9AfsTer94, The gene TECPR2 has a mutation status of L393AfsTer40, The gene AHNAK2 has a mutation status of V2471L, The gene UBR1 has a mutation status of S1178N, The gene DENND4A has a mutation status of D1235A, The gene RCN2 has a mutation status of E210del, The gene ADAMTSL3 has a mutation status of L476M, The gene ASB7 has a mutation status of L146V, The gene TMEM186 has a mutation status of R73DfsTer2, The gene ZNF319 has a mutation status of E511K, The gene PLEKHG4 has a mutation status of A502S, The gene ATXN1L has a mutation status of R610K, The gene ATP2C2 has a mutation status of I817del, The gene NLGN2 has a mutation status of L806PfsTer190, The gene TP53 has a mutation status of P152AfsTer14, The gene MYH1 has a mutation status of L167M, The gene CNTNAP1 has a mutation status of F598V, The gene PRKAR1A has a mutation status of D227G, The gene FAAP100 has a mutation status of R59G, The gene ZNF599 has a mutation status of F572V, The gene MAP3K10 has a mutation status of P193A, The gene CIC has a mutation status of K921N, The gene LILRB1 has a mutation status of Q401L, The gene SSC5D has a mutation status of G791DfsTer32, The gene ZSCAN5A has a mutation status of V169L, The gene ZNF417 has a mutation status of K537Ter, The gene EFR3B has a mutation status of A463V, The gene DPYSL5 has a mutation status of E41K, The gene USP34 has a mutation status of P497H, The gene OTX1 has a mutation status of M2I, The gene ZNF638 has a mutation status of S191F, The gene TBC1D8 has a mutation status of I220T, The gene SLC9A4 has a mutation status of S42RfsTer18, The gene TTN has a mutation status of W3448Ter, The gene DLGAP4 has a mutation status of Q518H, The gene TP53TG5 has a mutation status of S83F, The gene SLC2A4RG has a mutation status of R7H, The gene KRTAP19-5 has a mutation status of S57G, The gene RIPK4 has a mutation status of L778F, The gene IGLV2-33 has a mutation status of R66Ter, The gene CRELD2 has a mutation status of S295A, The gene MON1A has a mutation status of H154TfsTer8, The gene NISCH has a mutation status of Y1169Ter, The gene DPPA2 has a mutation status of M216I, The gene GCSAM has a mutation status of Y80D, The gene ADIPOQ has a mutation status of D231V, The gene TMEM207 has a mutation status of F130V, The gene XXYLT1 has a mutation status of A121V, The gene MUC4 has a mutation status of A3481L, The gene MUC4 has a mutation status of L1410H, The gene GRPEL1 has a mutation status of H175Y, The gene WDFY3 has a mutation status of A3401V, The gene HPGDS has a mutation status of I21R, The gene RBM46 has a mutation status of E22Ter, The gene CTNND2 has a mutation status of Y1019H, The gene SREK1IP1 has a mutation status of L87K, The gene APC has a mutation status of M526L, The gene RBM27 has a mutation status of R174L, The gene FAT2 has a mutation status of V170L, The gene WWC1 has a mutation status of E310D, The gene MBOAT1 has a mutation status of P440T, The gene HLA-C has a mutation status of L127G, The gene HLA-DQA1 has a mutation status of E73L, The gene COL12A1 has a mutation status of G2963E, The gene MFSD4B has a mutation status of L182Y, The gene FYN has a mutation status of E419TfsTer51, The gene PRKN has a mutation status of Q347H, The gene MAD1L1 has a mutation status of F629L, The gene JAZF1 has a mutation status of F10del, The gene GLI3 has a mutation status of I1504V, The gene RFC2 has a mutation status of Y322C, The gene MUC3A has a mutation status of V1672D, The gene TES has a mutation status of P299T, The gene CFTR has a mutation status of L986V, The gene ADAM2 has a mutation status of D538E, The gene C8orf88 has a mutation status of Q69H, The gene UBR5 has a mutation status of Q1410_K1412del, The gene MED30 has a mutation status of C103WfsTer23, The gene COL14A1 has a mutation status of Y1090Ter, The gene FAM205C has a mutation status of E196Ter, The gene SMC2 has a mutation status of K1178N, The gene PMPCA has a mutation status of V59A, The gene NOTCH1 has a mutation status of C254Ter, The gene NDOR1 has a mutation status of T60S, The gene MT-ND4 has a mutation status of S407T, The gene MT-CYB has a mutation status of A191T, The gene ITIH6 has a mutation status of T221S, The gene MTMR8 has a mutation status of W407C, The gene NEXMIF has a mutation status of W258C, The gene CCDC160 has a mutation status of G276R, The gene NOL9 has a mutation status of G589IfsTer15, The gene CELA3A has a mutation status of P65L, The gene ARID1A has a mutation status of S1001del, The gene RLF has a mutation status of V1887A, The gene FOXO6 has a mutation status of P338DfsTer39, The gene TAL1 has a mutation status of A264G, The gene SPATA6 has a mutation status of T76A, The gene PATJ has a mutation status of N120S, The gene VCAM1 has a mutation status of K4NfsTer22, The gene KCNA3 has a mutation status of E262K, The gene CHIA has a mutation status of Y203C, The gene DENND2C has a mutation status of C675F, The gene VANGL1 has a mutation status of P498T, The gene TTF2 has a mutation status of T724HfsTer6, The gene MNDA has a mutation status of T244I, The gene ATP1A4 has a mutation status of H501P, The gene USH2A has a mutation status of R4392I, The gene OBSCN has a mutation status of V1245L, The gene SFTPA1 has a mutation status of P62L, The gene DNTT has a mutation status of T169A, The gene SORCS1 has a mutation status of S57PfsTer17, The gene SHTN1 has a mutation status of S552C, The gene RHOG has a mutation status of R66C, The gene CCDC86 has a mutation status of P118Q, The gene SPTBN2 has a mutation status of A1641V, The gene C11orf24 has a mutation status of H73R, The gene SHANK2 has a mutation status of E1283RfsTer17, The gene KCTD21 has a mutation status of E199del, The gene DYNC2H1 has a mutation status of F948LfsTer9, The gene APOA5 has a mutation status of S212R, The gene CD3G has a mutation status of S148L, The gene TAS2R9 has a mutation status of K110Q, The gene IKZF4 has a mutation status of T443N, The gene TAFA2 has a mutation status of V85G, The gene LGR5 has a mutation status of P154A, The gene ZFC3H1 has a mutation status of A1913G, The gene PTPRQ has a mutation status of V537A, The gene HCFC2 has a mutation status of G496S, The gene DNAH10 has a mutation status of E523GfsTer22, The gene MRPL52 has a mutation status of S49Ter, The gene FOXG1 has a mutation status of T87M, The gene DPF3 has a mutation status of E162Ter, The gene ACOT2 has a mutation status of T185V, The gene PRIMA1 has a mutation status of V7CfsTer26, The gene TECPR2 has a mutation status of L393AfsTer40, The gene IGHV3-15 has a mutation status of E25Ter, The gene UBR1 has a mutation status of S1178N, The gene DENND4A has a mutation status of D1235A, The gene RCN2 has a mutation status of E210del, The gene ADAMTSL3 has a mutation status of L476M, The gene ASB7 has a mutation status of L146V, The gene NTN3 has a mutation status of R566W, The gene TMEM186 has a mutation status of R73DfsTer2, The gene USP7 has a mutation status of Q430K, The gene PDILT has a mutation status of V205A, The gene ITFG1 has a mutation status of S206F, The gene ZNF319 has a mutation status of E511K, The gene PLEKHG4 has a mutation status of A502S, The gene ATP2C2 has a mutation status of I817del, The gene TP53 has a mutation status of P152AfsTer14, The gene MYH1 has a mutation status of L167M, The gene TMEM238L has a mutation status of A52G, The gene CNTNAP1 has a mutation status of F598V, The gene PRKAR1A has a mutation status of D227G, The gene FAAP100 has a mutation status of R59G, The gene DCC has a mutation status of T461P, The gene MED26 has a mutation status of G236V, The gene ZNF599 has a mutation status of F572V, The gene MAP3K10 has a mutation status of P193A, The gene CIC has a mutation status of P153T, The gene CLASRP has a mutation status of R322S, The gene SPACA6 has a mutation status of V172I, The gene SSC5D has a mutation status of G791DfsTer32, The gene ZSCAN5A has a mutation status of V169L, The gene ZNF417 has a mutation status of K537Ter, The gene EFR3B has a mutation status of A463V, The gene USP34 has a mutation status of P497H, The gene OTX1 has a mutation status of M2I, The gene TBC1D8 has a mutation status of I220T, The gene AMER3 has a mutation status of L247F, The gene GALNT13 has a mutation status of K377E, The gene STK39 has a mutation status of T292I, The gene TTN has a mutation status of W3448Ter, The gene SUMO1 has a mutation status of E93Ter, The gene INO80D has a mutation status of Q355Ter, The gene DLGAP4 has a mutation status of Q518H, The gene TP53TG5 has a mutation status of S83F, The gene KRTAP19-5 has a mutation status of S57G, The gene HIRA has a mutation status of L355F, The gene ATXN10 has a mutation status of I350L, The gene MON1A has a mutation status of H154TfsTer8, The gene NISCH has a mutation status of Y1169Ter, The gene DPPA2 has a mutation status of M216I, The gene GCSAM has a mutation status of Y80D, The gene IGSF11 has a mutation status of K395R, The gene CFAP92 has a mutation status of A644V, The gene SI has a mutation status of I311M, The gene ADIPOQ has a mutation status of D231V, The gene TMEM207 has a mutation status of F130V, The gene XXYLT1 has a mutation status of A121V, The gene MUC4 has a mutation status of D2979_P3010del, The gene MUC4 has a mutation status of L1410H, The gene NSG1 has a mutation status of F8C, The gene GRPEL1 has a mutation status of H175Y, The gene FAM90A26 has a mutation status of C4VfsTer12, The gene FAM90A26 has a mutation status of R5H, The gene CLOCK has a mutation status of H821R, The gene WDFY3 has a mutation status of A3401V, The gene AP1AR has a mutation status of L220F, The gene CTNND2 has a mutation status of Y1019H, The gene MYO10 has a mutation status of S26T, The gene APC has a mutation status of M526L, The gene RBM27 has a mutation status of R174L, The gene FAT2 has a mutation status of V170L, The gene GEMIN5 has a mutation status of L1431V, The gene WWC1 has a mutation status of E310D, The gene RIOK1 has a mutation status of P483S, The gene TXNDC5 has a mutation status of L25_L26del, The gene MBOAT1 has a mutation status of P440T, The gene HLA-C has a mutation status of T162S, The gene HLA-C has a mutation status of A159D, The gene HLA-DQA1 has a mutation status of E73L, The gene EYS has a mutation status of N2473Y, The gene COL12A1 has a mutation status of G2963E, The gene BCKDHB has a mutation status of C106Y, The gene CASP8AP2 has a mutation status of W382L, The gene MFSD4B has a mutation status of L182Y, The gene FYN has a mutation status of E419TfsTer51, The gene IPCEF1 has a mutation status of G41S, The gene PRKN has a mutation status of Q347H, The gene MAD1L1 has a mutation status of F629L, The gene JAZF1 has a mutation status of F10del, The gene GLI3 has a mutation status of I1504V, The gene ZNF804B has a mutation status of H274Q, The gene MUC3A has a mutation status of V1672D, The gene TES has a mutation status of P299T, The gene CFTR has a mutation status of L986V, The gene KMT2C has a mutation status of P3390S, The gene UNC5D has a mutation status of E173HfsTer2, The gene SNAI2 has a mutation status of W198G, The gene NCOA2 has a mutation status of P1336S, The gene C8orf88 has a mutation status of Q69H, The gene UBR5 has a mutation status of Q1410_K1412del, The gene MED30 has a mutation status of C103WfsTer23, The gene COL14A1 has a mutation status of Y1090Ter, The gene IL33 has a mutation status of C58Ter, The gene TEX10 has a mutation status of L793TfsTer62, The gene NDOR1 has a mutation status of T60S, The gene MT-ND5 has a mutation status of G541S, The gene MTMR8 has a mutation status of W407C, The gene NEXMIF has a mutation status of W258C, The gene ATRX has a mutation status of S1841_I1842insHSL, The gene PAK3 has a mutation status of C371G, The gene CCDC160 has a mutation status of G276R	SARC
The gene MAN1C1 has a mutation status of K22T, The gene TMEM125 has a mutation status of L106du, The gene C1orf87 has a mutation status of T284I, The gene ROR1 has a mutation status of M1?, The gene NEXN has a mutation status of G29A, The gene AGL has a mutation status of Y596F, The gene NRAS has a mutation status of G12D, The gene SEMA6C has a mutation status of D29E, The gene LAMC1 has a mutation status of G81V, The gene DYRK3 has a mutation status of P520R, The gene SERTAD4 has a mutation status of A188T, The gene AKR1C8 has a mutation status of F171delinsLLRNYCMSQARTer, The gene ZNF503 has a mutation status of L610R, The gene TM9SF3 has a mutation status of L411I, The gene SCT has a mutation status of M1?, The gene ASCL3 has a mutation status of A137S, The gene DKK3 has a mutation status of A27T, The gene PRDM11 has a mutation status of L436R, The gene CREB3L1 has a mutation status of M153L, The gene PRPF19 has a mutation status of A482T, The gene GAL3ST3 has a mutation status of L23P, The gene RBM14 has a mutation status of A130T, The gene LRP5 has a mutation status of T267N, The gene DYNC2H1 has a mutation status of R3319C, The gene PTHLH has a mutation status of A19T, The gene MUC19 has a mutation status of T3551A, The gene MUC19 has a mutation status of N5779D, The gene TAMALIN has a mutation status of L298R, The gene ALX1 has a mutation status of A294S, The gene PLEKHG7 has a mutation status of F556L, The gene EP400 has a mutation status of A30delinsGPP, The gene EP400 has a mutation status of P581M, The gene RCBTB2 has a mutation status of G171E, The gene SLC7A7 has a mutation status of F148V, The gene DAAM1 has a mutation status of K144N, The gene ASB2 has a mutation status of A278G, The gene IGHV1-58 has a mutation status of A116_A117insSE, The gene TLN2 has a mutation status of E2410V, The gene SLC24A1 has a mutation status of S274R, The gene THOC6 has a mutation status of G158W, The gene VASN has a mutation status of V566I, The gene TANGO6 has a mutation status of L873I, The gene BCAR1 has a mutation status of A350S, The gene SYCE1L has a mutation status of N192T, The gene CDH13 has a mutation status of N472I, The gene SLC38A8 has a mutation status of L301F, The gene GSE1 has a mutation status of K2T, The gene FBXO31 has a mutation status of V129M, The gene ANKRD11 has a mutation status of S1271W, The gene TEKT1 has a mutation status of F220L, The gene TP53 has a mutation status of P153AfsTer28, The gene TP53 has a mutation status of T125=, The gene CHD3 has a mutation status of K282T, The gene MYH13 has a mutation status of E219K, The gene MYH3 has a mutation status of E1706K, The gene GPR179 has a mutation status of Y324H, The gene HEXIM2 has a mutation status of E269G, The gene ARHGAP27 has a mutation status of P423L, The gene BRIP1 has a mutation status of R762P, The gene LLGL2 has a mutation status of A307D, The gene MYO15B has a mutation status of K410N, The gene CELF4 has a mutation status of A402T, The gene ALPK2 has a mutation status of I743N, The gene HCN2 has a mutation status of L61V, The gene AKAP8L has a mutation status of D303H, The gene GTPBP3 has a mutation status of F349V, The gene ZNF492 has a mutation status of F364P, The gene KCTD15 has a mutation status of F219V, The gene SCAF1 has a mutation status of Q489H, The gene ZNF160 has a mutation status of R248Ter, The gene LILRB3 has a mutation status of W205Q, The gene APOB has a mutation status of G3617AfsTer6, The gene SPDYA has a mutation status of M305I, The gene PDCL3 has a mutation status of G186S, The gene MBD5 has a mutation status of I784M, The gene ACVR1 has a mutation status of H320Y, The gene TTN has a mutation status of I35361T, The gene PMS1 has a mutation status of A755S, The gene ALPI has a mutation status of G62W, The gene UGT1A7 has a mutation status of N129R, The gene CDH22 has a mutation status of S720R, The gene NCOA3 has a mutation status of Q1000Ter, The gene LAMA5 has a mutation status of K312Q, The gene ADAMTS1 has a mutation status of A68V, The gene PCNT has a mutation status of R1646SfsTer22, The gene ATP6V1E1 has a mutation status of T159N, The gene CSF2RB has a mutation status of Y593D, The gene MPST has a mutation status of P180R, The gene PANX2 has a mutation status of K485Q, The gene MAPK11 has a mutation status of M1?, The gene NGLY1 has a mutation status of T85A, The gene EOMES has a mutation status of T131P, The gene PTH1R has a mutation status of S473F, The gene PLXNB1 has a mutation status of A831D, The gene FRMD4B has a mutation status of R719G, The gene CSNKA2IP has a mutation status of C155S, The gene SLC9C1 has a mutation status of L561V, The gene ZNF148 has a mutation status of D300N, The gene SI has a mutation status of W1826Ter, The gene MUC4 has a mutation status of T1951_P1952insSLPVTDASSVSTGHATSLPVTSLSSVSTGDTTPLPVTSPSSASSGHTT, The gene SULT1E1 has a mutation status of E156G, The gene NDNF has a mutation status of Y557Ter, The gene NPY5R has a mutation status of H178R, The gene OSMR has a mutation status of W645R, The gene ARHGAP26 has a mutation status of I40L, The gene HTR4 has a mutation status of I303F, The gene SH3TC2 has a mutation status of L786R, The gene SLIT3 has a mutation status of I301V, The gene F12 has a mutation status of Y151H, The gene SLC22A23 has a mutation status of N24T, The gene SLC22A23 has a mutation status of E23A, The gene DNAH8 has a mutation status of K3553Q, The gene MRPS18A has a mutation status of L180V, The gene TPBG has a mutation status of V105L, The gene MOXD1 has a mutation status of S536P, The gene LRP11 has a mutation status of Q86P, The gene AFDN has a mutation status of Q592P, The gene MIOS has a mutation status of D439V, The gene TAX1BP1 has a mutation status of S467A, The gene MUC17 has a mutation status of V1697A, The gene COPG2 has a mutation status of N403I, The gene EZH2 has a mutation status of H279Y, The gene PAXIP1 has a mutation status of D774G, The gene CSMD1 has a mutation status of Y2427F, The gene SDR16C5 has a mutation status of I254T, The gene C8orf34 has a mutation status of M1?, The gene NUDCD1 has a mutation status of P31A, The gene ATAD2 has a mutation status of K504R, The gene MAFA has a mutation status of L5R, The gene PTCH1 has a mutation status of R571Q, The gene C9orf50 has a mutation status of V71G, The gene SETX has a mutation status of P1638T, The gene GTF3C4 has a mutation status of K33T, The gene NOTCH1 has a mutation status of Q2459Ter, The gene NELFB has a mutation status of E32D, The gene ARSD has a mutation status of N182H, The gene LAS1L has a mutation status of K31T, The gene SERPINA7 has a mutation status of V199D, The gene ATP2B3 has a mutation status of H1071P	DLBC
The gene CFAP74 has a mutation status of R835G, The gene MASP2 has a mutation status of Y401C, The gene HSPG2 has a mutation status of G2973D, The gene HIVEP3 has a mutation status of K79R, The gene SLC6A9 has a mutation status of W196Ter, The gene GBP6 has a mutation status of A610V, The gene AHCYL1 has a mutation status of P498L, The gene FLG has a mutation status of H2009N, The gene ENTREP3 has a mutation status of R547H, The gene POU2F1 has a mutation status of E36RfsTer23, The gene RC3H1 has a mutation status of I909S, The gene TNN has a mutation status of R140H, The gene TNR has a mutation status of A460T, The gene HMCN1 has a mutation status of L3855F, The gene OR2L2 has a mutation status of Q6E, The gene MALRD1 has a mutation status of L708V, The gene PTEN has a mutation status of I101T, The gene CARS1 has a mutation status of K616RfsTer75, The gene CARNS1 has a mutation status of G178V, The gene TCIRG1 has a mutation status of P511T, The gene PHLDB1 has a mutation status of R1184Q, The gene GRAMD1B has a mutation status of R861S, The gene TAS2R43 has a mutation status of H93RfsTer35, The gene GPR84 has a mutation status of F76L, The gene XPOT has a mutation status of Q192LfsTer5, The gene RB1 has a mutation status of R320Ter, The gene DLGAP5 has a mutation status of P727H, The gene TRMT5 has a mutation status of R8M, The gene HHIPL1 has a mutation status of R687L, The gene AHNAK2 has a mutation status of V2471L, The gene SPINT1 has a mutation status of E177D, The gene MGA has a mutation status of L664F, The gene FRMD5 has a mutation status of V215M, The gene TP53 has a mutation status of Y236C, The gene MPRIP has a mutation status of S251R, The gene ACACA has a mutation status of D1794E, The gene TANC2 has a mutation status of D831E, The gene SCN4A has a mutation status of M1753I, The gene UNC13D has a mutation status of D206G, The gene APC2 has a mutation status of A1828D, The gene ZNF763 has a mutation status of V209F, The gene OR10H3 has a mutation status of C142F, The gene EML2 has a mutation status of I108N, The gene ZNF432 has a mutation status of E83Q, The gene OSR1 has a mutation status of R136H, The gene NEURL3 has a mutation status of Y221Ter, The gene MERTK has a mutation status of T795A, The gene SCN2A has a mutation status of K1260Q, The gene FAM171B has a mutation status of T482I, The gene PMS1 has a mutation status of P302YfsTer3, The gene ORC2 has a mutation status of H176Y, The gene COL4A4 has a mutation status of L1381F, The gene NPEPL1 has a mutation status of L79Q, The gene ZNF512B has a mutation status of R681C, The gene KLHL22 has a mutation status of V147E, The gene SRRD has a mutation status of E304Ter, The gene ASCC2 has a mutation status of E544DfsTer10, The gene TNFRSF13C has a mutation status of G64V, The gene CCR4 has a mutation status of I83V, The gene ZNF654 has a mutation status of S646C, The gene TFG has a mutation status of A274G, The gene PIK3CB has a mutation status of A515T, The gene ATR has a mutation status of D836E, The gene ZIC4 has a mutation status of A187G, The gene TRIM59 has a mutation status of P4T, The gene NWD2 has a mutation status of P697S, The gene GABRB1 has a mutation status of D164A, The gene USO1 has a mutation status of E640del, The gene C4orf54 has a mutation status of T72P, The gene MCC has a mutation status of V223M, The gene RAD50 has a mutation status of N598I, The gene PSD2 has a mutation status of Q433E, The gene DELE1 has a mutation status of A69D, The gene OR2V1 has a mutation status of A255T, The gene DCDC2 has a mutation status of R452T, The gene HLA-A has a mutation status of G314C, The gene MUC21 has a mutation status of T323V, The gene ABCC10 has a mutation status of L34P, The gene ECT2L has a mutation status of L52FfsTer5, The gene PHACTR2 has a mutation status of E152D, The gene PHACTR2 has a mutation status of S369N, The gene SFT2D1 has a mutation status of W36Ter, The gene TNRC18 has a mutation status of S1628G, The gene GLI3 has a mutation status of S1028I, The gene MUC3A has a mutation status of T1234A, The gene MKLN1 has a mutation status of V490L, The gene KIAA1549 has a mutation status of A768S, The gene KMT2C has a mutation status of R3398Q, The gene UBR5 has a mutation status of C2768HfsTer12, The gene SCRIB has a mutation status of R1067L, The gene DMRT2 has a mutation status of V440A, The gene IFNE has a mutation status of G100V, The gene PCSK5 has a mutation status of D1811N, The gene LHX6 has a mutation status of Y365F, The gene MT-ND3 has a mutation status of G29S, The gene MED12 has a mutation status of H1822Q, The gene MED12 has a mutation status of R1871Ter, The gene AMOT has a mutation status of T709A, The gene MAGEC3 has a mutation status of M270K	GBMLGG
The gene VPS13D has a mutation status of D3451G, The gene HSPG2 has a mutation status of Y3908P, The gene MYOM3 has a mutation status of Q84P, The gene CRYBG2 has a mutation status of N240T, The gene CSMD2 has a mutation status of H1353R, The gene PRKAA2 has a mutation status of A191V, The gene TM2D1 has a mutation status of L51F, The gene AMPD2 has a mutation status of R33PfsTer51, The gene ZNF697 has a mutation status of R448H, The gene ATF6 has a mutation status of C380_N391del, The gene ADCY10 has a mutation status of D37Y, The gene LHX9 has a mutation status of R132S, The gene ZNF281 has a mutation status of T64P, The gene LRRN2 has a mutation status of T585P, The gene SUSD4 has a mutation status of Y394D, The gene OBSCN has a mutation status of D1110G, The gene AKR1C3 has a mutation status of M151V, The gene SLC39A12 has a mutation status of Y140N, The gene ADAMTS14 has a mutation status of T26P, The gene ADAMTS14 has a mutation status of A949T, The gene RBMXL2 has a mutation status of R335L, The gene DCDC1 has a mutation status of S125A, The gene OR8U1 has a mutation status of L131M, The gene OR8U1 has a mutation status of M155V, The gene CCDC88B has a mutation status of E235D, The gene RBM4B has a mutation status of G319D, The gene B3GNT6 has a mutation status of A172GfsTer61, The gene NOX4 has a mutation status of H342P, The gene ENDOD1 has a mutation status of V481F, The gene IQSEC3 has a mutation status of A566G, The gene PIK3C2G has a mutation status of N87S, The gene SMAGP has a mutation status of S27F, The gene ACVR1B has a mutation status of P26S, The gene MYL6B has a mutation status of D53H, The gene ZNF664 has a mutation status of H47Q, The gene SETDB2 has a mutation status of Q162K, The gene STK24 has a mutation status of E221K, The gene YLPM1 has a mutation status of Y8Ter, The gene TTC7B has a mutation status of I839T, The gene RIN3 has a mutation status of V371A, The gene CHRNA3 has a mutation status of Y236C, The gene PKD1 has a mutation status of Q3955P, The gene TIGD7 has a mutation status of A106T, The gene LONP2 has a mutation status of A345S, The gene DHX38 has a mutation status of Q759K, The gene CHST5 has a mutation status of R15Ter, The gene DBNDD1 has a mutation status of N101K, The gene TP53 has a mutation status of V147D, The gene MYH10 has a mutation status of G1125D, The gene ZNF18 has a mutation status of Q224K, The gene AKAP10 has a mutation status of S269P, The gene TOP2A has a mutation status of S1392Ter, The gene STAT5A has a mutation status of S777P, The gene VAT1 has a mutation status of D101A, The gene WNT9B has a mutation status of G85S, The gene KCNH6 has a mutation status of F700EfsTer5, The gene KCNH6 has a mutation status of F704_S706del, The gene DDX5 has a mutation status of G136V, The gene CD300LD has a mutation status of W2G, The gene CD7 has a mutation status of G86D, The gene ANKRD12 has a mutation status of R1734T, The gene WDR7 has a mutation status of Y81C, The gene ZNF407 has a mutation status of T1697A, The gene DOCK6 has a mutation status of Q1550R, The gene GMIP has a mutation status of A955T, The gene HSPB6 has a mutation status of A151P, The gene CAPN12 has a mutation status of F367L, The gene MAP3K10 has a mutation status of E423G, The gene DMWD has a mutation status of S225L, The gene KPTN has a mutation status of E40G, The gene ZNF256 has a mutation status of H210Y, The gene C2orf16 has a mutation status of E3942A, The gene HNRNPLL has a mutation status of Y186N, The gene THUMPD2 has a mutation status of E157del, The gene CLHC1 has a mutation status of E292DfsTer7, The gene PTCD3 has a mutation status of I396T, The gene RNF103 has a mutation status of R663W, The gene HOXD13 has a mutation status of A57G, The gene ZNF385B has a mutation status of K44T, The gene PARD3B has a mutation status of Q637H, The gene CDK5R2 has a mutation status of T127P, The gene RESP18 has a mutation status of G145V, The gene SCYGR4 has a mutation status of M1?, The gene TRPM8 has a mutation status of E402D, The gene SH3BP4 has a mutation status of K644R, The gene ATRN has a mutation status of Y1037C, The gene SNTA1 has a mutation status of A367P, The gene RIMS4 has a mutation status of A41T, The gene ZNF334 has a mutation status of E514Ter, The gene COL9A3 has a mutation status of V84G, The gene KCNQ2 has a mutation status of R691C, The gene RUNX1 has a mutation status of R76S, The gene MORC3 has a mutation status of Q913Ter, The gene BRWD1 has a mutation status of L1179V, The gene PACSIN2 has a mutation status of F120L, The gene MAPK8IP2 has a mutation status of A544G, The gene RAF1 has a mutation status of A42I, The gene RBSN has a mutation status of T214P, The gene CLASP2 has a mutation status of L907F, The gene TRANK1 has a mutation status of M2744I, The gene KLHL40 has a mutation status of R48C, The gene GASK1A has a mutation status of T163K, The gene GMPS has a mutation status of S378C, The gene CLDN16 has a mutation status of L75P, The gene MUC4 has a mutation status of V2825A, The gene SLBP has a mutation status of H161Q, The gene SLC30A9 has a mutation status of W258C, The gene PALLD has a mutation status of G340VfsTer15, The gene PALLD has a mutation status of L345IfsTer14, The gene GPM6A has a mutation status of T76A, The gene C4orf47 has a mutation status of S234Y, The gene LIFR has a mutation status of A985S, The gene LCP2 has a mutation status of P280S, The gene OR2V2 has a mutation status of L223V, The gene HLA-F has a mutation status of S113A, The gene HLA-A has a mutation status of K292E, The gene HLA-DQA1 has a mutation status of E73L, The gene PI16 has a mutation status of S48P, The gene PGC has a mutation status of V6G, The gene CD109 has a mutation status of I434N, The gene SOGA3 has a mutation status of A93RfsTer33, The gene L3MBTL3 has a mutation status of P225S, The gene IGF2R has a mutation status of S1048Ter, The gene SLC22A1 has a mutation status of L192I, The gene TMEM184A has a mutation status of V264F, The gene GRIFIN has a mutation status of L132R, The gene FOXK1 has a mutation status of T602P, The gene HOXA5 has a mutation status of N120K, The gene GLI3 has a mutation status of Y858S, The gene PCLO has a mutation status of S4293C, The gene RUNDC3B has a mutation status of I161V, The gene NAMPT has a mutation status of V266I, The gene KCNB2 has a mutation status of E592K, The gene CSMD3 has a mutation status of R395Q, The gene MTSS1 has a mutation status of E516D, The gene NRBP2 has a mutation status of Q465P, The gene TESK1 has a mutation status of V82I, The gene EXOSC3 has a mutation status of E258VfsTer4, The gene ANKRD18A has a mutation status of L264P, The gene ECPAS has a mutation status of T115M, The gene GSN has a mutation status of T547P, The gene NUP188 has a mutation status of Y1074S, The gene ABCA2 has a mutation status of L345V, The gene DPP7 has a mutation status of R307L, The gene MT-CYB has a mutation status of A330T	OV
The gene SKI has a mutation status of P352L, The gene RCC2 has a mutation status of G465R, The gene EVA1B has a mutation status of P141L, The gene DAB1 has a mutation status of G527E, The gene BCAR3 has a mutation status of P74H, The gene CELSR2 has a mutation status of R2015K, The gene MIA3 has a mutation status of L504F, The gene LBR has a mutation status of A301V, The gene DISC1 has a mutation status of R233G, The gene GREM2 has a mutation status of I30L, The gene NRG3 has a mutation status of Q360K, The gene NAALAD2 has a mutation status of S565F, The gene FAT3 has a mutation status of R3910H, The gene CDKN1B has a mutation status of C99GfsTer22, The gene HDAC7 has a mutation status of G75V, The gene PRIM1 has a mutation status of T133A, The gene R3HDM2 has a mutation status of F456delinsYI, The gene R3HDM2 has a mutation status of F456V, The gene FNTB has a mutation status of C345Y, The gene MAP1A has a mutation status of S2723R, The gene HERC1 has a mutation status of I720SfsTer12, The gene IGDCC4 has a mutation status of S463Y, The gene PIAS1 has a mutation status of F407LfsTer45, The gene NOX5 has a mutation status of R220P, The gene ISLR2 has a mutation status of N474D, The gene CCDC33 has a mutation status of N71D, The gene TTLL13 has a mutation status of E114GfsTer3, The gene CHSY1 has a mutation status of D450N, The gene NME3 has a mutation status of G39C, The gene CASKIN1 has a mutation status of L1205P, The gene GLG1 has a mutation status of W110LfsTer19, The gene MON1B has a mutation status of L218I, The gene TP53 has a mutation status of V272M, The gene RHBDL3 has a mutation status of L197V, The gene KRT32 has a mutation status of P427I, The gene KLHL10 has a mutation status of V203G, The gene CSH2 has a mutation status of L127M, The gene POLRMT has a mutation status of Q331Ter, The gene DNMT1 has a mutation status of V1555M, The gene DNM2 has a mutation status of V219SfsTer27, The gene FCGBP has a mutation status of G1230_P1231del, The gene FCGBP has a mutation status of S1228MfsTer5, The gene GYS1 has a mutation status of Q267K, The gene CNOT3 has a mutation status of L190Q, The gene MYCN has a mutation status of P44L, The gene C2orf16 has a mutation status of Q1094R, The gene BIRC6 has a mutation status of D60G, The gene FER1L5 has a mutation status of F1070L, The gene HS6ST1 has a mutation status of V26G, The gene FAM83D has a mutation status of L108M, The gene PAXBP1 has a mutation status of V8G, The gene IL17RA has a mutation status of V669M, The gene FBLN2 has a mutation status of P409S, The gene CAMKV has a mutation status of Q195K, The gene ITIH1 has a mutation status of A494T, The gene PTX3 has a mutation status of D21G, The gene MUC4 has a mutation status of A2446_T2468del, The gene PPARGC1A has a mutation status of T691A, The gene RFC1 has a mutation status of S621C, The gene FAT4 has a mutation status of S173F, The gene DNAH5 has a mutation status of R3079Ter, The gene C7 has a mutation status of K771Q, The gene SOWAHA has a mutation status of S37R, The gene PURA has a mutation status of A50G, The gene DIAPH1 has a mutation status of S264Y, The gene HMGXB3 has a mutation status of H797Y, The gene CARMIL1 has a mutation status of R1246Q, The gene H3C8 has a mutation status of K37R, The gene SCAND3 has a mutation status of R54C, The gene DDR1 has a mutation status of H25R, The gene HLA-DRB1 has a mutation status of T106N, The gene HOXA1 has a mutation status of V320I, The gene LYN has a mutation status of A455T, The gene ACO1 has a mutation status of A433S, The gene MYORG has a mutation status of D354N, The gene MIGA2 has a mutation status of V331M, The gene KDM5C has a mutation status of G1124TfsTer18, The gene FRMPD3 has a mutation status of A247V	DLBC
The gene CCDC24 has a mutation status of A263V, The gene SEMA6C has a mutation status of F238Y, The gene RAB13 has a mutation status of N121S, The gene PRDX6 has a mutation status of F28L, The gene NAV1 has a mutation status of T2119_V2120insGPP, The gene JCAD has a mutation status of S1307N, The gene ALOX5 has a mutation status of A307D, The gene PSAP has a mutation status of D340V, The gene WEE1 has a mutation status of P240L, The gene CYP2R1 has a mutation status of L213Ter, The gene CYP2R1 has a mutation status of F147L, The gene WT1 has a mutation status of V268TfsTer32, The gene DDB1 has a mutation status of I1068M, The gene MAP3K11 has a mutation status of M289V, The gene ST14 has a mutation status of P132T, The gene WNK1 has a mutation status of Q201E, The gene ABCC9 has a mutation status of F1188_R1189delinsLG, The gene SPATS2 has a mutation status of Q435H, The gene KRT1 has a mutation status of S631C, The gene HOXC8 has a mutation status of K205E, The gene TIMELESS has a mutation status of L810P, The gene CKAP4 has a mutation status of R228Q, The gene FBXL3 has a mutation status of M329K, The gene TTC6 has a mutation status of I1866S, The gene SAMD4A has a mutation status of I113T, The gene FAM181A has a mutation status of S34Y, The gene AHNAK2 has a mutation status of N2143D, The gene APBA2 has a mutation status of P535S, The gene TYRO3 has a mutation status of K235AfsTer18, The gene MGA has a mutation status of K2027R, The gene RCCD1 has a mutation status of Q269R, The gene EDC4 has a mutation status of L16M, The gene EDC4 has a mutation status of L22M, The gene CNTNAP4 has a mutation status of G388R, The gene TMEM132E has a mutation status of R174G, The gene MRC2 has a mutation status of R899H, The gene MARCHF10 has a mutation status of V305M, The gene MYO15B has a mutation status of G474A, The gene DNM2 has a mutation status of R361Ter, The gene SIGLEC10 has a mutation status of P283T, The gene KIR2DS4 has a mutation status of A168G, The gene KIR2DS4 has a mutation status of A169P, The gene GMCL1 has a mutation status of L240S, The gene GPR39 has a mutation status of R197C, The gene FAM171B has a mutation status of I364T, The gene AOX1 has a mutation status of D1200H, The gene PARD3B has a mutation status of Q687K, The gene PLCB1 has a mutation status of K975N, The gene BPIFB3 has a mutation status of G165D, The gene LIPI has a mutation status of N453KfsTer21, The gene ADAMTS1 has a mutation status of D202H, The gene TRMT2A has a mutation status of V482L, The gene RAB36 has a mutation status of L191M, The gene RIBC2 has a mutation status of N138H, The gene RIBC2 has a mutation status of I140R, The gene CTDSPL has a mutation status of L251R, The gene HYAL2 has a mutation status of R379C, The gene ROBO2 has a mutation status of V649L, The gene SENP7 has a mutation status of C980G, The gene AP2M1 has a mutation status of G127D, The gene SLC2A9 has a mutation status of V77M, The gene FABP2 has a mutation status of M22NfsTer4, The gene ADAM29 has a mutation status of Q796P, The gene MAP1B has a mutation status of S1609C, The gene SLCO6A1 has a mutation status of D490N, The gene CAMK2A has a mutation status of V73I, The gene CASP8AP2 has a mutation status of Y914S, The gene WDR27 has a mutation status of V443L, The gene AMZ1 has a mutation status of D371H, The gene TRGJ2 has a mutation status of N2SfsTer2, The gene TRGJ2 has a mutation status of N2H, The gene ANKIB1 has a mutation status of S884Y, The gene MUC3A has a mutation status of S342G, The gene WNT16 has a mutation status of K63R, The gene ESCO2 has a mutation status of H34N, The gene ZFHX4 has a mutation status of G1755S, The gene ZFHX4 has a mutation status of P2678A, The gene DECR1 has a mutation status of V124D, The gene LRATD2 has a mutation status of Q52H, The gene DENND3 has a mutation status of R462SfsTer3, The gene TONSL has a mutation status of Q803Ter, The gene TAF1L has a mutation status of P516H, The gene FKTN has a mutation status of Y31NfsTer18, The gene NOTCH1 has a mutation status of P2474AfsTer4, The gene NOTCH1 has a mutation status of L1593P, The gene MT-ND1 has a mutation status of A4V, The gene ZMAT1 has a mutation status of D392Y, The gene LONRF3 has a mutation status of V228M, The gene SLC25A5 has a mutation status of T221R, The gene SASH3 has a mutation status of H181R, The gene PLXNB3 has a mutation status of P213S	DLBC
The gene AKR7A2 has a mutation status of H302Y, The gene FAM43B has a mutation status of G106R, The gene ZSCAN20 has a mutation status of P827S, The gene SFPQ has a mutation status of S128P, The gene SZT2 has a mutation status of Q154L, The gene ASB17 has a mutation status of Y57Ter, The gene ARNT has a mutation status of V612I, The gene CDC42BPA has a mutation status of L435V, The gene HEATR1 has a mutation status of I755F, The gene CDH23 has a mutation status of D2695A, The gene RPP30 has a mutation status of K72T, The gene PDCD4 has a mutation status of Q435Ter, The gene PNLIP has a mutation status of W5G, The gene WDR11 has a mutation status of A663T, The gene PAOX has a mutation status of A24V, The gene MUC5AC has a mutation status of A5353K, The gene UBQLNL has a mutation status of E318NfsTer45, The gene SPON1 has a mutation status of A111T, The gene SLC43A3 has a mutation status of G3V, The gene EHBP1L1 has a mutation status of V893F, The gene PDE3A has a mutation status of V193G, The gene PDE3A has a mutation status of V194G, The gene RAPGEF3 has a mutation status of R706G, The gene KRT76 has a mutation status of Q220Ter, The gene RNF17 has a mutation status of A970V, The gene ATP4B has a mutation status of N146K, The gene NAA30 has a mutation status of E174K, The gene ZC3H14 has a mutation status of P346L, The gene PAPOLA has a mutation status of K543du, The gene IGHD has a mutation status of P162R, The gene OIP5 has a mutation status of L120P, The gene IQCH has a mutation status of P892L, The gene ACSBG1 has a mutation status of C11S, The gene ALG1 has a mutation status of I333V, The gene SNTB2 has a mutation status of V118G, The gene ZFP3 has a mutation status of C227Ter, The gene LLGL1 has a mutation status of V404A, The gene KRT32 has a mutation status of P427I, The gene FN3K has a mutation status of K269N, The gene LRRC30 has a mutation status of T246N, The gene VAPA has a mutation status of A2S, The gene SALL3 has a mutation status of A185L, The gene CAMSAP3 has a mutation status of F684T, The gene CLEC4G has a mutation status of L157P, The gene TSPAN16 has a mutation status of D192N, The gene KIRREL2 has a mutation status of N338T, The gene SLC6A16 has a mutation status of M148L, The gene ZNF888 has a mutation status of Q253E, The gene LILRB4 has a mutation status of K362P, The gene HS1BP3 has a mutation status of P181S, The gene LDAH has a mutation status of A86V, The gene TET3 has a mutation status of D177E, The gene LRRTM1 has a mutation status of T293N, The gene LRP2 has a mutation status of Q3770K, The gene LRP2 has a mutation status of G2470V, The gene INPP5D has a mutation status of L234M, The gene IQCA1 has a mutation status of V753M, The gene PIGU has a mutation status of L208F, The gene PABPC1L has a mutation status of P459T, The gene PREX1 has a mutation status of L1650I, The gene HELZ2 has a mutation status of H1468P, The gene ADAMTS5 has a mutation status of V319M, The gene PRDM15 has a mutation status of E185Ter, The gene PDE9A has a mutation status of L540R, The gene CCT8L2 has a mutation status of G474W, The gene IGLV2-14 has a mutation status of S116_T117insVVFGGG, The gene IGLV2-14 has a mutation status of L118KfsTer?, The gene RNF215 has a mutation status of L218W, The gene MCM5 has a mutation status of T166P, The gene EIF3L has a mutation status of H26Q, The gene POLDIP3 has a mutation status of S405F, The gene MSL2 has a mutation status of P389A, The gene B3GNT5 has a mutation status of Y353Ter, The gene UTS2B has a mutation status of S25F, The gene PAICS has a mutation status of I96T, The gene ARHGAP24 has a mutation status of R460K, The gene RAPGEF2 has a mutation status of N850KfsTer12, The gene NUP155 has a mutation status of K1197I, The gene EGFLAM has a mutation status of V318Ter, The gene MCTP1 has a mutation status of H128L, The gene PPT2 has a mutation status of L120V, The gene HLA-DRB5 has a mutation status of Q38W, The gene TBCC has a mutation status of V244L, The gene MAP3K7 has a mutation status of M392K, The gene FABP7 has a mutation status of V84I, The gene SOD2 has a mutation status of S139F, The gene INTS1 has a mutation status of W1368Ter, The gene BRAT1 has a mutation status of V425G, The gene EIF2AK1 has a mutation status of T297A, The gene MUC3A has a mutation status of A544_G545delinsDR, The gene CLDN23 has a mutation status of V5G, The gene CYP11B1 has a mutation status of P414A, The gene PLEC has a mutation status of A2135T, The gene WDR97 has a mutation status of A1281T, The gene TONSL has a mutation status of L945H, The gene ANKRD18B has a mutation status of E429Ter, The gene TDRD7 has a mutation status of S229P, The gene PRPF4 has a mutation status of C298S, The gene GLT6D1 has a mutation status of S127I, The gene CCDC187 has a mutation status of A384S, The gene MT-ND5 has a mutation status of A459V, The gene MT-ND5 has a mutation status of G460E, The gene MT-CYB has a mutation status of A380T, The gene MXRA5 has a mutation status of A1655T, The gene FAM47B has a mutation status of R4L, The gene PDZD4 has a mutation status of T519P	DLBC
The gene PERM1 has a mutation status of G165V, The gene SKI has a mutation status of E490K, The gene CNR2 has a mutation status of R302Q, The gene LDLRAP1 has a mutation status of S245R, The gene CRYBG2 has a mutation status of P837H, The gene TGFBR3 has a mutation status of V605L, The gene CELF3 has a mutation status of Q320K, The gene TNN has a mutation status of G1132D, The gene ASTN1 has a mutation status of M1068I, The gene LGR6 has a mutation status of I198T, The gene PLXNA2 has a mutation status of D1025Y, The gene IRF6 has a mutation status of L436EfsTer66, The gene IRF6 has a mutation status of Q435AfsTer67, The gene SYT14 has a mutation status of E356KfsTer11, The gene HHIPL2 has a mutation status of G502R, The gene ENAH has a mutation status of E202G, The gene ZSWIM8 has a mutation status of L628V, The gene DLG5 has a mutation status of D45G, The gene GHITM has a mutation status of V333I, The gene ANKRD1 has a mutation status of K153I, The gene WBP1L has a mutation status of S217P, The gene TCERG1L has a mutation status of P266L, The gene NAV2 has a mutation status of C1906W, The gene DGKZ has a mutation status of P282H, The gene MYBPC3 has a mutation status of G953_A954insVG, The gene OR5D13 has a mutation status of D123N, The gene INCENP has a mutation status of A130G, The gene ROM1 has a mutation status of L114V, The gene INTS5 has a mutation status of S727F, The gene POU2AF3 has a mutation status of K14N, The gene IGSF9B has a mutation status of T249P, The gene SCNN1A has a mutation status of R181W, The gene CLEC7A has a mutation status of S137P, The gene KRAS has a mutation status of G12V, The gene LRRK2 has a mutation status of N202Y, The gene TMEM106C has a mutation status of R46G, The gene MARCHF9 has a mutation status of A163P, The gene CHST11 has a mutation status of F182N, The gene HIP1R has a mutation status of A327G, The gene SLC15A4 has a mutation status of T438P, The gene ULK1 has a mutation status of K237M, The gene SACS has a mutation status of E4213RfsTer3, The gene GTF2F2 has a mutation status of V21K, The gene IRS2 has a mutation status of N201D, The gene ADPRHL1 has a mutation status of S1367Y, The gene ADPRHL1 has a mutation status of H415Q, The gene ZFHX2 has a mutation status of A122T, The gene NKX2-8 has a mutation status of R84S, The gene SIX6 has a mutation status of Y71C, The gene GALNT16 has a mutation status of S491C, The gene KIF26A has a mutation status of H1652Q, The gene TMEM121 has a mutation status of M19V, The gene TYRO3 has a mutation status of S559_S560insTDIIAS, The gene RORA has a mutation status of N114S, The gene ALPK3 has a mutation status of S33I, The gene ALPK3 has a mutation status of V1071A, The gene CACNA1H has a mutation status of A7T, The gene IGFALS has a mutation status of A603T, The gene PKD1 has a mutation status of Q4216K, The gene UBALD1 has a mutation status of T105P, The gene SEC14L5 has a mutation status of E348V, The gene RMI2 has a mutation status of S126C, The gene SRCAP has a mutation status of T1715S, The gene PLLP has a mutation status of S13G, The gene PLLP has a mutation status of R11W, The gene KATNB1 has a mutation status of C250W, The gene TAT has a mutation status of R57G, The gene ADAMTS18 has a mutation status of A870PfsTer28, The gene TP53 has a mutation status of T125=, The gene MYH2 has a mutation status of V884E, The gene MIEF2 has a mutation status of S273R, The gene SSH2 has a mutation status of R8W, The gene STAC2 has a mutation status of C186S, The gene KRT19 has a mutation status of Y61S, The gene TSPOAP1 has a mutation status of V258L, The gene RNF43 has a mutation status of R330HfsTer89, The gene HELZ has a mutation status of E760G, The gene CYGB has a mutation status of A82P, The gene CYGB has a mutation status of H81P, The gene SIRT7 has a mutation status of K310N, The gene RNMT has a mutation status of P422S, The gene ZBTB7C has a mutation status of C369Ter, The gene ONECUT2 has a mutation status of H297P, The gene TMX3 has a mutation status of D323E, The gene CCDC102B has a mutation status of V465WfsTer4, The gene CCDC102B has a mutation status of V465AfsTer5, The gene MUC16 has a mutation status of S11018T, The gene TYK2 has a mutation status of D429P, The gene HOOK2 has a mutation status of E484V, The gene CPAMD8 has a mutation status of V433M, The gene NCAN has a mutation status of S346P, The gene ZNF100 has a mutation status of H331D, The gene ALKBH6 has a mutation status of D116Y, The gene FCGBP has a mutation status of S772P, The gene NUMBL has a mutation status of R504L, The gene ZNF226 has a mutation status of F428L, The gene RUVBL2 has a mutation status of V389L, The gene LILRB2 has a mutation status of A595P, The gene ZNF8 has a mutation status of T370S, The gene GDF7 has a mutation status of A135G, The gene ALMS1 has a mutation status of A1410S, The gene GPR45 has a mutation status of A123P, The gene CNTNAP5 has a mutation status of S501T, The gene TNS1 has a mutation status of R242Ter, The gene VIL1 has a mutation status of T684A, The gene ZNF142 has a mutation status of A478P, The gene FEV has a mutation status of V83G, The gene FEV has a mutation status of F75V, The gene EIF4E2 has a mutation status of Q235Ter, The gene TP53RK has a mutation status of Q41H, The gene PREX1 has a mutation status of P765L, The gene ADAMTS1 has a mutation status of E58G, The gene MCM3AP has a mutation status of F1584L, The gene ESS2 has a mutation status of V244A, The gene MPST has a mutation status of F209L, The gene DENND6B has a mutation status of D178Ter, The gene MAPK8IP2 has a mutation status of G238C, The gene SHANK3 has a mutation status of L1586M, The gene CTDSPL has a mutation status of H200Y, The gene SCAP has a mutation status of Y407Ter, The gene CELSR3 has a mutation status of E1857G, The gene NISCH has a mutation status of A693V, The gene GOLGB1 has a mutation status of L3098W, The gene GFM1 has a mutation status of A641S, The gene RBM47 has a mutation status of M161I, The gene AMBN has a mutation status of T404I, The gene FAT4 has a mutation status of V2783I, The gene NKD2 has a mutation status of A157T, The gene UGT3A2 has a mutation status of A439P, The gene FBN2 has a mutation status of M631V, The gene SLC22A5 has a mutation status of S190L, The gene CATSPER3 has a mutation status of G147A, The gene SLC25A48 has a mutation status of L177MfsTer15, The gene PCDHGC3 has a mutation status of L801V, The gene GRIA1 has a mutation status of R698W, The gene HAND1 has a mutation status of S141N, The gene FOXC1 has a mutation status of L518_N519delinsFY, The gene PSMG4 has a mutation status of V5G, The gene SNRNP48 has a mutation status of G37R, The gene SNRNP48 has a mutation status of D44H, The gene GFOD1 has a mutation status of T52L, The gene NHLRC1 has a mutation status of T125A, The gene GABBR1 has a mutation status of R923L, The gene MUC21 has a mutation status of T323V, The gene HLA-DRB5 has a mutation status of Q38W, The gene HLA-DQB2 has a mutation status of V37Y, The gene HLA-DOA has a mutation status of A44P, The gene ITPR3 has a mutation status of L2635V, The gene BRPF3 has a mutation status of G1029C, The gene TBC1D22B has a mutation status of R421L, The gene FBXO9 has a mutation status of R85P, The gene MCM9 has a mutation status of R132L, The gene NOX3 has a mutation status of C327A, The gene IGF2R has a mutation status of C830F, The gene THBS2 has a mutation status of V6G, The gene MPLKIP has a mutation status of Q107L, The gene NACAD has a mutation status of A622P, The gene ZNF273 has a mutation status of H224R, The gene VGF has a mutation status of G250V, The gene VGF has a mutation status of E243Ter, The gene FLNC has a mutation status of V231G, The gene MYOM2 has a mutation status of L1346V, The gene RP1 has a mutation status of K722E, The gene CDH17 has a mutation status of Y131N, The gene RIMS2 has a mutation status of R1474G, The gene FER1L6 has a mutation status of I1817du, The gene EEF1D has a mutation status of E45G, The gene PARP10 has a mutation status of G951A, The gene OPLAH has a mutation status of M746I, The gene MROH1 has a mutation status of E260G, The gene CDKN2A has a mutation status of T18_A19du, The gene SHB has a mutation status of A214D, The gene ECPAS has a mutation status of K846R, The gene CRB2 has a mutation status of H157Y, The gene CRB2 has a mutation status of H1094Y, The gene ABL1 has a mutation status of G1060D, The gene RALGDS has a mutation status of C178W, The gene FBXW5 has a mutation status of D531L, The gene NELFB has a mutation status of G593V, The gene MT-ND3 has a mutation status of G40S, The gene MAGEB3 has a mutation status of N147I, The gene MAGEB1 has a mutation status of Q23Ter, The gene TFE3 has a mutation status of A312P, The gene ZXDA has a mutation status of T310A, The gene AMER1 has a mutation status of F685S, The gene PAK3 has a mutation status of E96Ter	PAAD
The gene TTLL10 has a mutation status of P604T, The gene PIK3CD has a mutation status of T739P, The gene UBXN10 has a mutation status of M34V, The gene ARID1A has a mutation status of F2141LfsTer9, The gene SYTL1 has a mutation status of Q3H, The gene TMEM54 has a mutation status of V71I, The gene MYSM1 has a mutation status of D382EfsTer30, The gene LRRC7 has a mutation status of A754T, The gene ABCD3 has a mutation status of R266S, The gene OLFM3 has a mutation status of H415IfsTer48, The gene CHD1L has a mutation status of Y871Ter, The gene TNR has a mutation status of R899Q, The gene ABL2 has a mutation status of P109L, The gene BRINP3 has a mutation status of E421K, The gene ASCL5 has a mutation status of H206N, The gene KMO has a mutation status of I224V, The gene EXO1 has a mutation status of A671V, The gene NEBL has a mutation status of M782I, The gene EBLN1 has a mutation status of G28W, The gene PARD3 has a mutation status of R294Q, The gene ASAH2 has a mutation status of F394S, The gene ABRAXAS2 has a mutation status of Q183Ter, The gene SCART1 has a mutation status of S658Ter, The gene TRPM5 has a mutation status of G541V, The gene MADD has a mutation status of E1337D, The gene OR5I1 has a mutation status of A119T, The gene CTNND1 has a mutation status of I747V, The gene MS4A14 has a mutation status of A309S, The gene DDB1 has a mutation status of L1000V, The gene P2RY6 has a mutation status of V102F, The gene THRSP has a mutation status of P76S, The gene HEPHL1 has a mutation status of C366Y, The gene NXPE4 has a mutation status of N279T, The gene PDE3A has a mutation status of G953F, The gene KRAS has a mutation status of G12V, The gene XPOT has a mutation status of R778L, The gene DRAM1 has a mutation status of H122N, The gene BICDL1 has a mutation status of D233Y, The gene ACADS has a mutation status of P85S, The gene ZNF605 has a mutation status of T97A, The gene SLC25A15 has a mutation status of V156L, The gene ACOD1 has a mutation status of L128F, The gene SLAIN1 has a mutation status of S181Ter, The gene TMTC4 has a mutation status of F290C, The gene OR4K5 has a mutation status of Y193F, The gene RNASE11 has a mutation status of A134S, The gene PRKD1 has a mutation status of Q876Ter, The gene SAMD4A has a mutation status of T462P, The gene GPR135 has a mutation status of A461G, The gene SPTB has a mutation status of L567Q, The gene SPTBN5 has a mutation status of E3265Q, The gene TTBK2 has a mutation status of P487A, The gene MYO5A has a mutation status of A1846T, The gene CILP has a mutation status of W155Ter, The gene RHBDL1 has a mutation status of S5Ter, The gene RNF40 has a mutation status of R742C, The gene CHD9 has a mutation status of I317M, The gene ZFHX3 has a mutation status of Q3197SfsTer45, The gene ZFHX3 has a mutation status of P3195LfsTer44, The gene ATMIN has a mutation status of M309V, The gene PKD1L2 has a mutation status of T1446K, The gene ANKRD11 has a mutation status of Y2438C, The gene WDR81 has a mutation status of R786M, The gene PLSCR3 has a mutation status of F66LfsTer18, The gene TP53 has a mutation status of P153AfsTer28, The gene MYH3 has a mutation status of R704C, The gene TRPV2 has a mutation status of L479R, The gene SLC47A1 has a mutation status of E529K, The gene SARM1 has a mutation status of A234P, The gene BLTP2 has a mutation status of A15S, The gene ABHD15 has a mutation status of S235R, The gene MEOX1 has a mutation status of Q13H, The gene ANKFN1 has a mutation status of I593F, The gene FOXJ1 has a mutation status of D58Y, The gene LRRC45 has a mutation status of L177M, The gene SMAD4 has a mutation status of E538Ter, The gene CACNA1A has a mutation status of T665M, The gene PODNL1 has a mutation status of E440Ter, The gene CILP2 has a mutation status of M952I, The gene ZNF676 has a mutation status of K279NfsTer219, The gene TDRD12 has a mutation status of Q1124K, The gene ZNF585B has a mutation status of N525H, The gene TMEM143 has a mutation status of T308P, The gene SCAF1 has a mutation status of R928S, The gene SIGLEC5 has a mutation status of L334I, The gene SIGLEC5 has a mutation status of S333Y, The gene KIR2DS4 has a mutation status of E127G, The gene FKBP1B has a mutation status of E4D, The gene THADA has a mutation status of S1933T, The gene PRKCE has a mutation status of N108K, The gene ADRA2B has a mutation status of W137AfsTer80, The gene TMEM131 has a mutation status of P494R, The gene LONRF2 has a mutation status of Q210H, The gene ARHGEF4 has a mutation status of P829T, The gene TANC1 has a mutation status of D1703G, The gene FIGN has a mutation status of P723T, The gene MAP3K20 has a mutation status of S599P, The gene AGPS has a mutation status of P29T, The gene OSGEPL1 has a mutation status of T44I, The gene ANKZF1 has a mutation status of S517N, The gene SLC19A3 has a mutation status of S381T, The gene NGEF has a mutation status of R110Ter, The gene PER2 has a mutation status of V175L, The gene PLCB1 has a mutation status of Q593K, The gene MACROD2 has a mutation status of M413I, The gene DZANK1 has a mutation status of Q298Ter, The gene PDRG1 has a mutation status of D50N, The gene GSS has a mutation status of T299S, The gene PTPRT has a mutation status of P489S, The gene KRTAP27-1 has a mutation status of R10I, The gene RCAN1 has a mutation status of V28G, The gene CACNA1I has a mutation status of Q1798P, The gene CAND2 has a mutation status of A499I, The gene NICN1 has a mutation status of I135SfsTer11, The gene ITIH3 has a mutation status of P26R, The gene GATA2 has a mutation status of H51Y, The gene TRH has a mutation status of D179E, The gene SLC2A2 has a mutation status of R432P, The gene IL1RAP has a mutation status of I302V, The gene MUC4 has a mutation status of V3305_S3336del, The gene MELTF has a mutation status of S59Y, The gene LCORL has a mutation status of G1642R, The gene PGM2 has a mutation status of A329T, The gene CEP44 has a mutation status of G30F, The gene CCDC110 has a mutation status of S775I, The gene CCDC127 has a mutation status of V199F, The gene C5orf34 has a mutation status of P29L, The gene HTR1A has a mutation status of K412E, The gene ADGRV1 has a mutation status of G1589R, The gene SMIM32 has a mutation status of L20V, The gene PCDHA11 has a mutation status of D409Y, The gene HRH2 has a mutation status of Y78Ter, The gene COL23A1 has a mutation status of E73Ter, The gene COL23A1 has a mutation status of A67S, The gene MUC21 has a mutation status of T323V, The gene HLA-DRB1 has a mutation status of W38E, The gene RNF8 has a mutation status of M25G, The gene COL19A1 has a mutation status of I133M, The gene MMS22L has a mutation status of I948V, The gene AKAP7 has a mutation status of E197A, The gene PRR18 has a mutation status of P226A, The gene MRM2 has a mutation status of G73S, The gene SNX8 has a mutation status of A18S, The gene AGR3 has a mutation status of T127A, The gene DNAH11 has a mutation status of E566D, The gene HYCC1 has a mutation status of N417T, The gene CLIP2 has a mutation status of L419M, The gene LAMB4 has a mutation status of N1574K, The gene AOC1 has a mutation status of V192L, The gene ZNF703 has a mutation status of H421P, The gene ASH2L has a mutation status of H538R, The gene TGS1 has a mutation status of S96G, The gene CHD7 has a mutation status of M123_V125delinsI, The gene NECAB1 has a mutation status of N107D, The gene UBR5 has a mutation status of V848A, The gene HGH1 has a mutation status of V159G, The gene SCRT1 has a mutation status of S16P, The gene AUH has a mutation status of R87L, The gene DNAJC25 has a mutation status of E281D, The gene ASTN2 has a mutation status of Y1244H, The gene DAB2IP has a mutation status of L1081M, The gene SPACA9 has a mutation status of L103V, The gene KLHL15 has a mutation status of Y91Ter, The gene USP51 has a mutation status of T223N, The gene TAF1 has a mutation status of R1009H, The gene COL4A5 has a mutation status of P1094S	PAAD
The gene MXRA8 has a mutation status of V214G, The gene PTPRF has a mutation status of L1128P, The gene C8B has a mutation status of T342PfsTer19, The gene KANK4 has a mutation status of A593S, The gene AP4B1 has a mutation status of H446L, The gene TRIM33 has a mutation status of Y974H, The gene GJA8 has a mutation status of D3N, The gene PIP5K1A has a mutation status of L165PfsTer4, The gene RGL1 has a mutation status of E657V, The gene ASPM has a mutation status of Y1146C, The gene KIF26B has a mutation status of E995D, The gene KIF26B has a mutation status of L996P, The gene ASB13 has a mutation status of K261N, The gene PTCHD3 has a mutation status of W139R, The gene CCNY has a mutation status of L84V, The gene PIK3AP1 has a mutation status of A364V, The gene CALHM1 has a mutation status of G87S, The gene INPP5F has a mutation status of R69Q, The gene CHST15 has a mutation status of N441S, The gene RNH1 has a mutation status of D47Y, The gene MUC6 has a mutation status of Y277S, The gene CCDC88B has a mutation status of R246G, The gene ARHGEF17 has a mutation status of G257A, The gene RSF1 has a mutation status of S1364T, The gene FKBP4 has a mutation status of P119S, The gene GALNT8 has a mutation status of E387V, The gene MUC19 has a mutation status of I6366K, The gene FAIM2 has a mutation status of C223F, The gene DIP2B has a mutation status of Q876R, The gene KCNC2 has a mutation status of E136K, The gene GLIPR1L1 has a mutation status of P110A, The gene CFAP54 has a mutation status of T2256R, The gene HCFC2 has a mutation status of E384Q, The gene GIT2 has a mutation status of R142I, The gene CUX2 has a mutation status of A755T, The gene HS6ST3 has a mutation status of V468G, The gene CUL4A has a mutation status of N383D, The gene SLC24A4 has a mutation status of P365R, The gene CCNK has a mutation status of V410L, The gene TLNRD1 has a mutation status of T223I, The gene WDR93 has a mutation status of H236L, The gene MESP2 has a mutation status of K254N, The gene MYLK3 has a mutation status of A233V, The gene DRC7 has a mutation status of S327T, The gene CMTM2 has a mutation status of P141T, The gene SLC12A4 has a mutation status of C781F, The gene NXN has a mutation status of Y199D, The gene BCL6B has a mutation status of P368Q, The gene LLGL1 has a mutation status of R734Ter, The gene ATP6V0A1 has a mutation status of E107K, The gene ABCA5 has a mutation status of E449K, The gene DSG4 has a mutation status of M148V, The gene ASXL3 has a mutation status of F1023Y, The gene MAPK4 has a mutation status of V259G, The gene SALL3 has a mutation status of A185L, The gene ATP8B3 has a mutation status of S781Ter, The gene NFIC has a mutation status of T384M, The gene PTPRS has a mutation status of F1169L, The gene C3 has a mutation status of K1375Q, The gene MYO1F has a mutation status of F525L, The gene CACNA1A has a mutation status of L1701P, The gene CACNA1A has a mutation status of Q1673K, The gene ZNF431 has a mutation status of R571K, The gene KIRREL2 has a mutation status of N338T, The gene ZNF841 has a mutation status of L245F, The gene PTPRH has a mutation status of C245F, The gene NLRP11 has a mutation status of N813S, The gene RPS5 has a mutation status of E98K, The gene EMILIN1 has a mutation status of R706S, The gene EHD3 has a mutation status of A534S, The gene NEB has a mutation status of E7717G, The gene SCN1A has a mutation status of L1634V, The gene TTN has a mutation status of M1187I, The gene CYP20A1 has a mutation status of C326S, The gene TRIP12 has a mutation status of E668Q, The gene ASB18 has a mutation status of A327G, The gene LTN1 has a mutation status of D1370G, The gene SCAF4 has a mutation status of P722du, The gene IL17RA has a mutation status of E186K, The gene IGLC3 has a mutation status of P76L, The gene MN1 has a mutation status of A1226T, The gene NPTXR has a mutation status of A172P, The gene XRCC6 has a mutation status of G138R, The gene SLC4A7 has a mutation status of S704N, The gene CSPG5 has a mutation status of R398S, The gene PLXNB1 has a mutation status of D236G, The gene ADPRH has a mutation status of W289L, The gene MUC4 has a mutation status of A4086T, The gene MUC4 has a mutation status of P3312S, The gene SLIT2 has a mutation status of F1354Y, The gene SMARCA5 has a mutation status of G35S, The gene LRBA has a mutation status of L849R, The gene FHDC1 has a mutation status of L754M, The gene TKTL2 has a mutation status of G470E, The gene FAM151B has a mutation status of A75S, The gene ANKRD34B has a mutation status of T442A, The gene OR2V2 has a mutation status of M165I, The gene DSP has a mutation status of A2148S, The gene CAP2 has a mutation status of V353A, The gene TRIM39 has a mutation status of R238Q, The gene HLA-C has a mutation status of L294C, The gene HLA-C has a mutation status of T187E, The gene HLA-DRB1 has a mutation status of S66N, The gene GFRAL has a mutation status of A329E, The gene ZNF451 has a mutation status of F221C, The gene PRDM13 has a mutation status of Y288S, The gene SERINC1 has a mutation status of M61I, The gene TAAR5 has a mutation status of P68L, The gene OPRM1 has a mutation status of R55T, The gene FAM120B has a mutation status of R105S, The gene ELFN1 has a mutation status of R240P, The gene EGFR has a mutation status of L858R, The gene PRRT4 has a mutation status of S533A, The gene NOBOX has a mutation status of D154H, The gene YTHDF3 has a mutation status of P83R, The gene RALYL has a mutation status of R158S, The gene PTP4A3 has a mutation status of P112T, The gene PRUNE2 has a mutation status of L318I, The gene WNK2 has a mutation status of V461G, The gene OR1L4 has a mutation status of T215S, The gene FCN2 has a mutation status of D4N, The gene MT-ND5 has a mutation status of G582D, The gene BMP15 has a mutation status of F314L, The gene HUWE1 has a mutation status of R1676H, The gene WNK3 has a mutation status of A536T, The gene ARMCX1 has a mutation status of G126W, The gene HS6ST2 has a mutation status of T25P, The gene F8 has a mutation status of L646Ter	LUAD
The gene HIVEP3 has a mutation status of R2082W, The gene IPP has a mutation status of I392M, The gene CDC42BPA has a mutation status of R1310C, The gene EXO1 has a mutation status of R93K, The gene ODAD2 has a mutation status of N664S, The gene NCOA4 has a mutation status of K329Ter, The gene BMPR1A has a mutation status of Q3P, The gene EXOSC1 has a mutation status of G101E, The gene DMBT1 has a mutation status of A165V, The gene C10orf90 has a mutation status of D258TfsTer47, The gene MUC5AC has a mutation status of L4460PfsTer11, The gene OR52I2 has a mutation status of L17F, The gene OVCH2 has a mutation status of P328A, The gene ABTB2 has a mutation status of R711G, The gene OR5I1 has a mutation status of R263W, The gene HNRNPUL2 has a mutation status of G340A, The gene SYT12 has a mutation status of E232K, The gene RNF121 has a mutation status of L56F, The gene RDX has a mutation status of D298H, The gene ERC1 has a mutation status of K643Q, The gene A2M has a mutation status of H358Y, The gene TAS2R31 has a mutation status of K150_E151delinsNQ, The gene SLCO1B1 has a mutation status of L337SfsTer38, The gene GXYLT1 has a mutation status of C414H, The gene DDN has a mutation status of G525A, The gene FAM222A has a mutation status of A176V, The gene TPCN1 has a mutation status of T743N, The gene MORN3 has a mutation status of E228A, The gene POLE has a mutation status of K1550R, The gene ZNF84 has a mutation status of W90C, The gene CDX2 has a mutation status of L249S, The gene CLDN10 has a mutation status of A71P, The gene ATP11A has a mutation status of I79T, The gene RIPK3 has a mutation status of L242WfsTer14, The gene RIPK3 has a mutation status of S241Ter, The gene AKAP6 has a mutation status of D235N, The gene RALGAPA1 has a mutation status of S1815F, The gene VCPKMT has a mutation status of E6Q, The gene OTX2 has a mutation status of P27H, The gene INO80 has a mutation status of S3L, The gene AGBL1 has a mutation status of F910L, The gene GNG13 has a mutation status of E33Q, The gene DNAAF8 has a mutation status of R196C, The gene MYH11 has a mutation status of D623G, The gene CDH1 has a mutation status of P484_P489del, The gene WFDC1 has a mutation status of S166T, The gene TP53 has a mutation status of R248Q, The gene ANKRD13B has a mutation status of N352S, The gene ABCA9 has a mutation status of D383N, The gene GRB2 has a mutation status of Y52N, The gene LAMA1 has a mutation status of D1247N, The gene C19orf53 has a mutation status of A19T, The gene ZNF99 has a mutation status of K124M, The gene ZNF91 has a mutation status of P1163S, The gene NFKBIB has a mutation status of A2V, The gene FCGBP has a mutation status of T1234_L1242del, The gene ZNF227 has a mutation status of P450S, The gene LILRB3 has a mutation status of W205Q, The gene LILRB3 has a mutation status of T201M, The gene ZNF460 has a mutation status of V50F, The gene DDX1 has a mutation status of K535T, The gene RAD51AP2 has a mutation status of E901Ter, The gene GEN1 has a mutation status of I203VfsTer17, The gene PSME4 has a mutation status of V106L, The gene SAP130 has a mutation status of V722F, The gene ZRANB3 has a mutation status of R272L, The gene ITGAV has a mutation status of R618L, The gene CXCR1 has a mutation status of S327I, The gene DNAJB2 has a mutation status of L126P, The gene TRIP12 has a mutation status of S361G, The gene PLCG1 has a mutation status of D315G, The gene SYNJ1 has a mutation status of Q1250R, The gene ADA2 has a mutation status of Y453H, The gene BCL2L13 has a mutation status of S80RfsTer35, The gene VILL has a mutation status of E448K, The gene SI has a mutation status of D671E, The gene BCHE has a mutation status of L456R, The gene LRRC31 has a mutation status of G408V, The gene JAKMIP1 has a mutation status of Q779H, The gene JAKMIP1 has a mutation status of L734M, The gene IGFBP7 has a mutation status of T188S, The gene TRAM1L1 has a mutation status of L202R, The gene DDX60L has a mutation status of P1366S, The gene ADCY2 has a mutation status of M693I, The gene TRPC7 has a mutation status of K738I, The gene PCDHAC2 has a mutation status of R267W, The gene PPP2R2B has a mutation status of M252_D259del, The gene ZNF354C has a mutation status of K438N, The gene MAML1 has a mutation status of H549Y, The gene FLT4 has a mutation status of E336K, The gene HLA-B has a mutation status of Y140L, The gene TRDN has a mutation status of S667T, The gene PTPRK has a mutation status of A6E, The gene VWC2 has a mutation status of A126V, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of M384T, The gene MUC3A has a mutation status of S395T, The gene MUC3A has a mutation status of T1234A, The gene PNPLA8 has a mutation status of Y583H, The gene HTR5A has a mutation status of R67H, The gene RP1L1 has a mutation status of L87P, The gene PDGFRL has a mutation status of E315D, The gene SLC26A7 has a mutation status of G200E, The gene TG has a mutation status of S1450R, The gene KCNK9 has a mutation status of V221M, The gene MELK has a mutation status of S486Ter, The gene TNC has a mutation status of A1055D, The gene PPP1R26 has a mutation status of S180N, The gene SLC25A5 has a mutation status of G121C, The gene SLC25A5 has a mutation status of T221R, The gene TENM1 has a mutation status of R1402C, The gene BCORL1 has a mutation status of G1756RfsTer4	STES
The gene AGMAT has a mutation status of Q264K, The gene SPEN has a mutation status of R1488I, The gene PHACTR4 has a mutation status of E513D, The gene RLF has a mutation status of T30S, The gene TMEM125 has a mutation status of P140A, The gene CYP4A22 has a mutation status of G417D, The gene PRKAA2 has a mutation status of P371T, The gene AMPD2 has a mutation status of R789H, The gene CD2 has a mutation status of C217Y, The gene SPTA1 has a mutation status of Q1581H, The gene CLEC20A has a mutation status of E386K, The gene COLGALT2 has a mutation status of V475I, The gene PLA2G4A has a mutation status of H442Q, The gene KLHDC8A has a mutation status of S277G, The gene DNAH14 has a mutation status of Q3628K, The gene EPHX1 has a mutation status of V392A, The gene TRIM11 has a mutation status of R37H, The gene DIP2C has a mutation status of V1264M, The gene TAF3 has a mutation status of P366LfsTer6, The gene ENKUR has a mutation status of D135V, The gene ANKRD26 has a mutation status of P483S, The gene ODAD2 has a mutation status of K332RfsTer32, The gene CCNY has a mutation status of G2W, The gene A1CF has a mutation status of T316S, The gene AVPI1 has a mutation status of Q32Ter, The gene SORCS1 has a mutation status of K223N, The gene ATRNL1 has a mutation status of N861T, The gene NUP98 has a mutation status of G1652V, The gene SMPD1 has a mutation status of S192P, The gene SMPD1 has a mutation status of A195P, The gene DNAJC24 has a mutation status of S103EfsTer2, The gene PTPRJ has a mutation status of H1104D, The gene OR1S1 has a mutation status of F215I, The gene CEP295 has a mutation status of L1096M, The gene TAS2R13 has a mutation status of N149S, The gene TAS2R43 has a mutation status of L193I, The gene SLC2A13 has a mutation status of S15I, The gene KRT1 has a mutation status of G116S, The gene PAN2 has a mutation status of E373VfsTer32, The gene INHBE has a mutation status of R62T, The gene PPP1R12A has a mutation status of Q767H, The gene HCAR1 has a mutation status of N56KfsTer6, The gene MYCBP2 has a mutation status of S3013Y, The gene GPR180 has a mutation status of T32N, The gene COL4A1 has a mutation status of T1449A, The gene NFKBIA has a mutation status of R143PfsTer11, The gene MIDEAS has a mutation status of S761TfsTer63, The gene WARS1 has a mutation status of E455D, The gene IGHV4-59 has a mutation status of E35Q, The gene SMG1 has a mutation status of K3583Q, The gene CHP2 has a mutation status of L122F, The gene TMEM219 has a mutation status of L200V, The gene ZNF423 has a mutation status of A112T, The gene ZNF469 has a mutation status of W3316Ter, The gene TP53 has a mutation status of G108del, The gene SLFN11 has a mutation status of L595S, The gene TRIM47 has a mutation status of F561LfsTer31, The gene ELP2 has a mutation status of L581AfsTer6, The gene CTIF has a mutation status of V389L, The gene MBD2 has a mutation status of G93C, The gene CYP4F3 has a mutation status of Q377E, The gene TMEM161A has a mutation status of E85L, The gene ZNF676 has a mutation status of H523R, The gene ZNF227 has a mutation status of K518_R519delinsNTer, The gene ZNF229 has a mutation status of Y377S, The gene APOC4 has a mutation status of P75Q, The gene BICRA has a mutation status of P651H, The gene MYBPC2 has a mutation status of P730L, The gene ZNF808 has a mutation status of Y595Ter, The gene PRPF31 has a mutation status of R365W, The gene AGBL5 has a mutation status of R487P, The gene LHCGR has a mutation status of D564N, The gene ANKRD36C has a mutation status of Y1082C, The gene DDX18 has a mutation status of G41R, The gene ARHGEF4 has a mutation status of T1627R, The gene SCN3A has a mutation status of E946G, The gene SP3 has a mutation status of G428S, The gene SLC4A3 has a mutation status of D431VfsTer13, The gene UGT1A4 has a mutation status of S446I, The gene ATG4B has a mutation status of D200IfsTer46, The gene SLC2A10 has a mutation status of V84A, The gene ITGB2 has a mutation status of V180EfsTer21, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene MYH9 has a mutation status of H1401del, The gene BAP1 has a mutation status of Q261Ter, The gene GPR15 has a mutation status of V252L, The gene GOLIM4 has a mutation status of A312L, The gene RTP1 has a mutation status of R124S, The gene MUC4 has a mutation status of T3942L, The gene NOA1 has a mutation status of Q579R, The gene BLTP1 has a mutation status of P1455S, The gene OTUD4 has a mutation status of G17AfsTer40, The gene OTUD4 has a mutation status of P8_G15delinsR, The gene TRIM61 has a mutation status of A448E, The gene PDCD6 has a mutation status of G123C, The gene C5orf34 has a mutation status of S266R, The gene CTNNA1 has a mutation status of Q678Ter, The gene PCDHB15 has a mutation status of A719V, The gene ADRB2 has a mutation status of E62D, The gene BOD1 has a mutation status of H96delinsLIVQFPSMSENKN, The gene GMCL2 has a mutation status of K247NfsTer8, The gene GMPR has a mutation status of E167K, The gene LY6G6F has a mutation status of P192R, The gene SKIC2 has a mutation status of L183V, The gene PRRT1 has a mutation status of A94T, The gene HLA-DQB1 has a mutation status of P84E, The gene HSD17B8 has a mutation status of V158L, The gene CYB5R4 has a mutation status of D371Y, The gene CEP85L has a mutation status of S30P, The gene GPNMB has a mutation status of S519I, The gene CCDC126 has a mutation status of E101D, The gene MUC3A has a mutation status of W18G, The gene MUC3A has a mutation status of G2238_P2254del, The gene FLNC has a mutation status of D205Y, The gene CNTNAP2 has a mutation status of T968S, The gene ABCB8 has a mutation status of A673G, The gene PAXIP1 has a mutation status of F491C, The gene PEBP4 has a mutation status of R149P, The gene ADRA1A has a mutation status of G40W, The gene ZBTB10 has a mutation status of A91V, The gene PRSS3 has a mutation status of D102I, The gene PRSS3 has a mutation status of G208R, The gene FRMPD1 has a mutation status of G572D, The gene TRMT10B has a mutation status of Y289L, The gene DNM1 has a mutation status of P816S, The gene MT-ND5 has a mutation status of S402P, The gene MT-ND6 has a mutation status of V164M, The gene SSX1 has a mutation status of L61Q, The gene HUWE1 has a mutation status of R481K, The gene ITIH6 has a mutation status of P76L, The gene ZXDA has a mutation status of E447G, The gene RPS4X has a mutation status of E97Q, The gene PLS3 has a mutation status of D485A	BRCA
The gene PERM1 has a mutation status of A769T, The gene FBXO44 has a mutation status of E59K, The gene KDM1A has a mutation status of K723R, The gene C1orf87 has a mutation status of E429Ter, The gene LRRIQ3 has a mutation status of T387S, The gene TGFBR3 has a mutation status of M491I, The gene CDC14A has a mutation status of V221A, The gene ALX3 has a mutation status of G256V, The gene ALX3 has a mutation status of G253V, The gene DENND4B has a mutation status of K1407N, The gene ARHGEF2 has a mutation status of R789M, The gene IQGAP3 has a mutation status of H755N, The gene TUBAL3 has a mutation status of G373W, The gene SKIDA1 has a mutation status of G892S, The gene RBP3 has a mutation status of P1241Q, The gene COL13A1 has a mutation status of P195Q, The gene KAT6B has a mutation status of S417T, The gene SMC3 has a mutation status of R967Ter, The gene STK32C has a mutation status of H214N, The gene MUC5AC has a mutation status of S4844Y, The gene OR51M1 has a mutation status of P266H, The gene USP47 has a mutation status of S1203P, The gene OR4A15 has a mutation status of L99R, The gene OR8I2 has a mutation status of G16V, The gene TM7SF2 has a mutation status of A49V, The gene FGF4 has a mutation status of S182N, The gene SERPINH1 has a mutation status of A87E, The gene SERPINH1 has a mutation status of A93D, The gene AMOTL1 has a mutation status of Q583K, The gene AMOTL1 has a mutation status of Q589K, The gene ZNF202 has a mutation status of R133Q, The gene LPAR5 has a mutation status of A288T, The gene TAS2R43 has a mutation status of N76C, The gene GUCY2C has a mutation status of Y397Ter, The gene PIK3C2G has a mutation status of G350W, The gene ADAMTS20 has a mutation status of E1424V, The gene NCKAP5L has a mutation status of G702V, The gene KRT72 has a mutation status of A63D, The gene PAN2 has a mutation status of K459R, The gene DPY19L2 has a mutation status of A462T, The gene HCAR1 has a mutation status of F55L, The gene EP400 has a mutation status of P581M, The gene MICU2 has a mutation status of K306L, The gene GRK1 has a mutation status of L145I, The gene AJUBA has a mutation status of G42R, The gene RNF31 has a mutation status of E32Ter, The gene L3HYPDH has a mutation status of G38V, The gene DYNC1H1 has a mutation status of E58Ter, The gene KIF26A has a mutation status of R1222S, The gene ADSS1 has a mutation status of E112K, The gene IGHV3-30 has a mutation status of S71R, The gene SPINT1 has a mutation status of E110Ter, The gene MGA has a mutation status of P608T, The gene MGA has a mutation status of P611T, The gene SPTBN5 has a mutation status of E2562K, The gene TLN2 has a mutation status of M160I, The gene CORO2B has a mutation status of W253L, The gene NPW has a mutation status of L89I, The gene IL4R has a mutation status of F395L, The gene SLC5A2 has a mutation status of P626Q, The gene SLC5A2 has a mutation status of L628I, The gene CNGB1 has a mutation status of E229D, The gene ANKRD11 has a mutation status of I433R, The gene CPNE7 has a mutation status of K356N, The gene GEMIN4 has a mutation status of P932H, The gene ASGR1 has a mutation status of Q29K, The gene SHBG has a mutation status of E133Ter, The gene TRPV2 has a mutation status of K680N, The gene SLC47A2 has a mutation status of R210S, The gene TNFAIP1 has a mutation status of E103Q, The gene CPD has a mutation status of V856G, The gene PLXDC1 has a mutation status of H103Q, The gene KRT32 has a mutation status of P427I, The gene WNK4 has a mutation status of P38S, The gene DBF4B has a mutation status of V89M, The gene ATP5F1A has a mutation status of Q286K, The gene POLI has a mutation status of R305L, The gene ONECUT2 has a mutation status of R9L, The gene RAX has a mutation status of E78D, The gene GZMM has a mutation status of Q74Ter, The gene BSG has a mutation status of Y106Ter, The gene PRTN3 has a mutation status of A196D, The gene DPP9 has a mutation status of P631H, The gene CAMSAP3 has a mutation status of S646Y, The gene MUC16 has a mutation status of E1706K, The gene CDKN2D has a mutation status of R25L, The gene RAB3D has a mutation status of F38CfsTer134, The gene SLC27A1 has a mutation status of G338V, The gene PIK3R2 has a mutation status of P184L, The gene RASGRP4 has a mutation status of R570S, The gene CEACAM18 has a mutation status of W63C, The gene ZNF628 has a mutation status of E19D, The gene MYCN has a mutation status of P109Q, The gene RAD51AP2 has a mutation status of M1150I, The gene MFSD2B has a mutation status of G351W, The gene DNMT3A has a mutation status of R882C, The gene ALK has a mutation status of T1312I, The gene DHX57 has a mutation status of R630Q, The gene TMEM127 has a mutation status of P51H, The gene ZEB2 has a mutation status of V31I, The gene COL5A2 has a mutation status of Q224H, The gene SNORC has a mutation status of P20T, The gene POFUT1 has a mutation status of W29L, The gene SOGA1 has a mutation status of E534Ter, The gene TGM2 has a mutation status of L673M, The gene PABPC1L has a mutation status of P448Q, The gene ARFGEF2 has a mutation status of A39E, The gene PRELID3B has a mutation status of T5N, The gene KREMEN1 has a mutation status of P332L, The gene SLC35E4 has a mutation status of G97E, The gene MFNG has a mutation status of Q98K, The gene CYP2D7 has a mutation status of W83L, The gene TTLL8 has a mutation status of R684C, The gene SBF1 has a mutation status of P271S, The gene GRM7 has a mutation status of I593V, The gene EMC3 has a mutation status of D41H, The gene ANKRD28 has a mutation status of V539A, The gene DENND6A has a mutation status of R15S, The gene MYH15 has a mutation status of G117R, The gene ESYT3 has a mutation status of E88Ter, The gene NSD2 has a mutation status of E1241Ter, The gene FRAS1 has a mutation status of V2518M, The gene TET2 has a mutation status of F1041IfsTer2, The gene TBCK has a mutation status of R530L, The gene SEC24D has a mutation status of D393N, The gene ARHGAP10 has a mutation status of H375N, The gene FNIP2 has a mutation status of G921V, The gene TENM3 has a mutation status of A2517S, The gene IRX2 has a mutation status of S236Ter, The gene PCDHGB4 has a mutation status of D337A, The gene PPARGC1B has a mutation status of F17L, The gene HLA-A has a mutation status of T104K, The gene HLA-B has a mutation status of Y140L, The gene LTB has a mutation status of L19H, The gene VWA7 has a mutation status of S774Y, The gene LRRC73 has a mutation status of G15S, The gene CRYBG1 has a mutation status of W406L, The gene CRYBG1 has a mutation status of M409I, The gene ADAT2 has a mutation status of L145P, The gene ULBP1 has a mutation status of K147T, The gene TBXT has a mutation status of L271I, The gene SNX8 has a mutation status of Q379H, The gene SLC29A4 has a mutation status of M1?, The gene FERD3L has a mutation status of E78K, The gene SP8 has a mutation status of T185N, The gene HOXA3 has a mutation status of Y6C, The gene MYO1G has a mutation status of E304Ter, The gene RFC2 has a mutation status of A150V, The gene FGL2 has a mutation status of C191Y, The gene SMURF1 has a mutation status of R7H, The gene FLNC has a mutation status of P2219T, The gene BRAF has a mutation status of V600E, The gene KRBA1 has a mutation status of E19Ter, The gene DPP6 has a mutation status of V438L, The gene KIF13B has a mutation status of E1319Ter, The gene WWP1 has a mutation status of K536E, The gene ZFAT has a mutation status of E1191Q, The gene ZFAT has a mutation status of A1185E, The gene GPIHBP1 has a mutation status of G18V, The gene PLEC has a mutation status of A4281V, The gene SHARPIN has a mutation status of P345H, The gene SMARCA2 has a mutation status of R346L, The gene ZCCHC7 has a mutation status of D307H, The gene FKBP15 has a mutation status of S548Y, The gene AMBP has a mutation status of K311T, The gene AKNA has a mutation status of V473L, The gene MEGF9 has a mutation status of G81W, The gene GARNL3 has a mutation status of N780K, The gene RAPGEF1 has a mutation status of R834M, The gene AK8 has a mutation status of G469V, The gene PAXX has a mutation status of S99Ter, The gene H2AP has a mutation status of S30I, The gene EBP has a mutation status of V163A, The gene GPKOW has a mutation status of E44D, The gene MED12 has a mutation status of L36P, The gene PDZD4 has a mutation status of P497H, The gene PDZD4 has a mutation status of S496G	LAML
The gene SPEN has a mutation status of K1600Ter, The gene SPEN has a mutation status of T2892IfsTer2, The gene ZMYM6 has a mutation status of C1141F, The gene EPHA10 has a mutation status of S300Ter, The gene SETDB1 has a mutation status of P5S, The gene FLG2 has a mutation status of S1062F, The gene IGFN1 has a mutation status of P11S, The gene ZBTB18 has a mutation status of L176S, The gene FZD8 has a mutation status of V382G, The gene ANTXRL has a mutation status of H61N, The gene CDH23 has a mutation status of D2695A, The gene CPEB3 has a mutation status of R270L, The gene FRAT1 has a mutation status of G187W, The gene FBXL15 has a mutation status of W24L, The gene NKX1-2 has a mutation status of D226N, The gene LMNTD2 has a mutation status of G496AfsTer38, The gene SMPD1 has a mutation status of S264N, The gene DNHD1 has a mutation status of P3322H, The gene RAB3IL1 has a mutation status of Y346C, The gene BEST1 has a mutation status of P103T, The gene GAL3ST3 has a mutation status of A377S, The gene KMT2A has a mutation status of K1751Ter, The gene VWF has a mutation status of N2546Y, The gene SMCO2 has a mutation status of L179M, The gene NCKAP1L has a mutation status of R214Q, The gene RIMBP2 has a mutation status of E1005D, The gene RIMBP2 has a mutation status of G1002V, The gene ZMYM5 has a mutation status of I83V, The gene SACS has a mutation status of V3345I, The gene CCDC168 has a mutation status of D4207E, The gene IPO4 has a mutation status of V31F, The gene FOXA1 has a mutation status of G378S, The gene VSX2 has a mutation status of P49Q, The gene KIF26A has a mutation status of P348Q, The gene FMN1 has a mutation status of S272A, The gene RPUSD2 has a mutation status of E228A, The gene TYRO3 has a mutation status of A28S, The gene SPTBN5 has a mutation status of Q2569K, The gene STARD9 has a mutation status of L4099I, The gene SYNM has a mutation status of K987R, The gene SH2B1 has a mutation status of P22T, The gene TAOK2 has a mutation status of N721S, The gene CNGB1 has a mutation status of S1017T, The gene MMP15 has a mutation status of V620G, The gene SNTB2 has a mutation status of V116G, The gene WWOX has a mutation status of P217S, The gene PLCG2 has a mutation status of E165K, The gene ZNF469 has a mutation status of G47C, The gene ZNF469 has a mutation status of R49S, The gene ZNF469 has a mutation status of P626H, The gene CDT1 has a mutation status of L314M, The gene FANCA has a mutation status of E1451K, The gene PITPNA has a mutation status of K5N, The gene DNAH2 has a mutation status of L1068P, The gene UNC45B has a mutation status of A676T, The gene KANSL1 has a mutation status of R748W, The gene CCDC47 has a mutation status of E329D, The gene CASKIN2 has a mutation status of P884Q, The gene CASKIN2 has a mutation status of S880P, The gene FOXJ1 has a mutation status of W38L, The gene TMC6 has a mutation status of G242C, The gene SETBP1 has a mutation status of P1539H, The gene MALT1 has a mutation status of A23D, The gene DSEL has a mutation status of L1117_L1118delinsFM, The gene MED16 has a mutation status of P705Q, The gene ABCA7 has a mutation status of T2023P, The gene DIRAS1 has a mutation status of V18G, The gene ZFR2 has a mutation status of P574R, The gene MICOS13 has a mutation status of G109C, The gene PNPLA6 has a mutation status of S1323Ter, The gene TYK2 has a mutation status of E824Ter, The gene DOCK6 has a mutation status of E1052K, The gene GTPBP3 has a mutation status of T53P, The gene B3GNT3 has a mutation status of P106R, The gene TMEM59L has a mutation status of P34T, The gene ZNF257 has a mutation status of A414P, The gene WTIP has a mutation status of E44Ter, The gene FCGBP has a mutation status of Q2163E, The gene FCGBP has a mutation status of T1234_L1242del, The gene FCGBP has a mutation status of S1228MfsTer5, The gene SPTBN4 has a mutation status of V1105P, The gene RELB has a mutation status of P314Q, The gene SIX5 has a mutation status of P471Q, The gene PRKD2 has a mutation status of T485I, The gene PRR12 has a mutation status of E1823Ter, The gene EPS8L1 has a mutation status of P456T, The gene TMEM18 has a mutation status of S81Ter, The gene C2orf81 has a mutation status of V324G, The gene HK2 has a mutation status of Q799R, The gene POU3F3 has a mutation status of P237S, The gene POU3F3 has a mutation status of G239W, The gene GLI2 has a mutation status of H974N, The gene LRP1B has a mutation status of K3585Q, The gene SP5 has a mutation status of D186N, The gene SP5 has a mutation status of P193T, The gene ITGAV has a mutation status of R333H, The gene MYO1B has a mutation status of N146H, The gene TNS1 has a mutation status of S1096C, The gene DES has a mutation status of P148S, The gene C2orf72 has a mutation status of V179E, The gene CHRND has a mutation status of V328HfsTer17, The gene GPC1 has a mutation status of Q385K, The gene ADAM33 has a mutation status of T701P, The gene SUN5 has a mutation status of T352I, The gene NEURL2 has a mutation status of F55I, The gene CTSZ has a mutation status of G228R, The gene CDH26 has a mutation status of V641L, The gene SEC14L2 has a mutation status of I264TfsTer11, The gene APOBEC3F has a mutation status of N31D, The gene TTC38 has a mutation status of L299P, The gene PPP6R2 has a mutation status of A486L, The gene RAF1 has a mutation status of A118CfsTer9, The gene DAZL has a mutation status of S33F, The gene GASK1A has a mutation status of D279E, The gene PFKFB4 has a mutation status of G122V, The gene CACNA1D has a mutation status of Q1370Ter, The gene CFAP44 has a mutation status of K1075RfsTer33, The gene PLXNA1 has a mutation status of R630L, The gene FAM184B has a mutation status of W26C, The gene SDAD1 has a mutation status of K209E, The gene SCARB2 has a mutation status of S20T, The gene HERC5 has a mutation status of V52G, The gene TACR3 has a mutation status of T389A, The gene NPNT has a mutation status of V417I, The gene PABPC4L has a mutation status of Y193Ter, The gene RNF180 has a mutation status of D287N, The gene F2R has a mutation status of R4G, The gene MAN2A1 has a mutation status of N738S, The gene PCDHAC1 has a mutation status of S290G, The gene CCDC69 has a mutation status of H163Q, The gene COL23A1 has a mutation status of D246Y, The gene DNAH8 has a mutation status of G2031V, The gene ZBTB24 has a mutation status of F378S, The gene EPB41L2 has a mutation status of A125S, The gene AHI1 has a mutation status of R548S, The gene SMIM28 has a mutation status of W9C, The gene LFNG has a mutation status of G58L, The gene VWDE has a mutation status of V1097L, The gene GLI3 has a mutation status of S1028I, The gene TECPR1 has a mutation status of G852W, The gene MUC3A has a mutation status of E725K, The gene CREB3L2 has a mutation status of G7W, The gene SHH has a mutation status of G297C, The gene SHH has a mutation status of G296W, The gene POLR3D has a mutation status of D306N, The gene SCARA5 has a mutation status of G214C, The gene CHRNB3 has a mutation status of V335I, The gene OPRK1 has a mutation status of W221Ter, The gene CDH17 has a mutation status of G511R, The gene ERMP1 has a mutation status of N421S, The gene MPDZ has a mutation status of E702M, The gene SIGMAR1 has a mutation status of W11L, The gene CCIN has a mutation status of V118A, The gene ZNF189 has a mutation status of C178Y, The gene TTLL11 has a mutation status of G56V, The gene TTLL11 has a mutation status of E52Ter, The gene PTRH1 has a mutation status of G128W, The gene MXRA5 has a mutation status of W7L, The gene BCOR has a mutation status of D1752Y, The gene NUDT11 has a mutation status of G50W, The gene HUWE1 has a mutation status of G1749D, The gene NLGN3 has a mutation status of E61Ter, The gene RADX has a mutation status of I532T, The gene PLXNB3 has a mutation status of P108Q	LAML
The gene HSPG2 has a mutation status of S2888Y, The gene CSMD2 has a mutation status of L1857P, The gene SFPQ has a mutation status of G265D, The gene TFAP2E has a mutation status of A8S, The gene TTF2 has a mutation status of P337T, The gene POGZ has a mutation status of L411R, The gene RYR2 has a mutation status of A165D, The gene RSU1 has a mutation status of L245H, The gene CUBN has a mutation status of E1096K, The gene HNRNPF has a mutation status of D110N, The gene CHAT has a mutation status of D250G, The gene DUSP13 has a mutation status of P28S, The gene SH2D4B has a mutation status of R391S, The gene GBF1 has a mutation status of Q1497LfsTer9, The gene CFAP46 has a mutation status of S2463I, The gene MUC5AC has a mutation status of C1146F, The gene SPTY2D1 has a mutation status of T111A, The gene MADD has a mutation status of I1349K, The gene PLCB3 has a mutation status of Q677Ter, The gene PRSS23 has a mutation status of H175D, The gene MTMR2 has a mutation status of A28EfsTer9, The gene GUCY1A2 has a mutation status of Q156K, The gene FGF23 has a mutation status of R175W, The gene ATN1 has a mutation status of Y530Ter, The gene KRAS has a mutation status of G12D, The gene LRIG3 has a mutation status of L86S, The gene HVCN1 has a mutation status of M91T, The gene MPHOSPH8 has a mutation status of P246S, The gene KPNA3 has a mutation status of F331TfsTer6, The gene MYCBP2 has a mutation status of H4186Y, The gene ANKRD9 has a mutation status of D149H, The gene ASPG has a mutation status of Y510H, The gene TJP1 has a mutation status of R22P, The gene SCAPER has a mutation status of I1217T, The gene CHRNB4 has a mutation status of L249V, The gene SLC7A6 has a mutation status of N149K, The gene TP53 has a mutation status of G245S, The gene DNAH9 has a mutation status of G4068R, The gene HEATR6 has a mutation status of A1021QfsTer37, The gene LAMA1 has a mutation status of E883Q, The gene GATA6 has a mutation status of L3F, The gene TMEM241 has a mutation status of L159F, The gene TPGS2 has a mutation status of I27M, The gene TPGS2 has a mutation status of T25A, The gene NCLN has a mutation status of R263S, The gene LONP1 has a mutation status of T644P, The gene FCHO1 has a mutation status of S454R, The gene LIPE has a mutation status of W543C, The gene SIX5 has a mutation status of G11V, The gene CNOT3 has a mutation status of P559L, The gene TDRD15 has a mutation status of V1251L, The gene STON1 has a mutation status of K654_Y668del, The gene IWS1 has a mutation status of E279K, The gene KCNJ3 has a mutation status of T90N, The gene FIGN has a mutation status of L374V, The gene TTN has a mutation status of Y9206F, The gene CCDC150 has a mutation status of T90NfsTer9, The gene PAX3 has a mutation status of R271C, The gene EIF4E2 has a mutation status of R140Q, The gene BPIFB3 has a mutation status of L233I, The gene DSCAM has a mutation status of E1274K, The gene SNAP29 has a mutation status of V128G, The gene POLDIP3 has a mutation status of T256A, The gene PDZRN3 has a mutation status of K81R, The gene GOLGB1 has a mutation status of N2291T, The gene TNIK has a mutation status of G34R, The gene TLR10 has a mutation status of K318R, The gene SLC9B1 has a mutation status of S334T, The gene DHX29 has a mutation status of G660V, The gene DEPDC1B has a mutation status of A308V, The gene ARSB has a mutation status of L336CfsTer2, The gene DND1 has a mutation status of R327Q, The gene PCDHB7 has a mutation status of A305V, The gene GARIN3 has a mutation status of E391D, The gene GFPT2 has a mutation status of N549K, The gene DSP has a mutation status of A2092SfsTer6, The gene OR2B8P has a mutation status of T176S, The gene HLA-DRB5 has a mutation status of Q38W, The gene SYNE1 has a mutation status of L4415I, The gene USP42 has a mutation status of I522L, The gene USP42 has a mutation status of N697H, The gene BBS9 has a mutation status of W10C, The gene PGAM2 has a mutation status of S189C, The gene SSC4D has a mutation status of R419L, The gene DLC1 has a mutation status of Q303R, The gene CCAR2 has a mutation status of Q689E, The gene SLCO5A1 has a mutation status of K497Ter, The gene PSKH2 has a mutation status of Y281C, The gene PKHD1L1 has a mutation status of T866N, The gene ASAP1 has a mutation status of A570T, The gene EEIG1 has a mutation status of T322M, The gene MT-ND5 has a mutation status of I283V, The gene MT-CYB has a mutation status of R100Q, The gene ASB11 has a mutation status of M1?, The gene AMER1 has a mutation status of A150G, The gene CDX4 has a mutation status of S135A, The gene ATP2B3 has a mutation status of L552V	PAAD
The gene RNF223 has a mutation status of A239D, The gene SCNN1D has a mutation status of E42Ter, The gene TNFRSF1B has a mutation status of A20E, The gene LSM10 has a mutation status of V104CfsTer35, The gene DNALI1 has a mutation status of N142K, The gene RIMKLA has a mutation status of R12H, The gene TRABD2B has a mutation status of R306C, The gene CLCA1 has a mutation status of R93I, The gene CLCA4 has a mutation status of E709G, The gene ADORA3 has a mutation status of L270M, The gene CD2 has a mutation status of H339L, The gene ATP1A4 has a mutation status of I117V, The gene NOS1AP has a mutation status of D135N, The gene IGFN1 has a mutation status of R2510S, The gene CAPN2 has a mutation status of N275K, The gene OBSCN has a mutation status of A5326D, The gene OBSCN has a mutation status of T8578I, The gene PNPLA2 has a mutation status of G483W, The gene PRPF19 has a mutation status of H273R, The gene GAB2 has a mutation status of M465I, The gene SLC37A4 has a mutation status of S22R, The gene SOX5 has a mutation status of M686T, The gene IGFBP6 has a mutation status of E46D, The gene MBD6 has a mutation status of P880L, The gene CFAP54 has a mutation status of V933G, The gene SVOP has a mutation status of T67N, The gene GCN1 has a mutation status of R1803W, The gene ADGRD1 has a mutation status of T758M, The gene CENPJ has a mutation status of P1104T, The gene RGCC has a mutation status of G8C, The gene DACH1 has a mutation status of P47RfsTer147, The gene NPAS3 has a mutation status of R64W, The gene RAB15 has a mutation status of A172V, The gene PAPOLA has a mutation status of P365S, The gene DPH6 has a mutation status of L187F, The gene NOX5 has a mutation status of Q725H, The gene CTXND1 has a mutation status of T18N, The gene CRAMP1 has a mutation status of G19C, The gene ACSM1 has a mutation status of G508V, The gene ZCCHC14 has a mutation status of P990H, The gene DPEP1 has a mutation status of R348M, The gene VPS9D1 has a mutation status of P252T, The gene CLUH has a mutation status of K210R, The gene ITGAE has a mutation status of C236R, The gene TP53 has a mutation status of R248W, The gene TRAF4 has a mutation status of R448Q, The gene NUFIP2 has a mutation status of T584A, The gene MMP28 has a mutation status of P453S, The gene DUSP3 has a mutation status of G127V, The gene DUSP3 has a mutation status of K79R, The gene FBF1 has a mutation status of R895W, The gene BAHCC1 has a mutation status of P330H, The gene CCDC102B has a mutation status of K419E, The gene FBN3 has a mutation status of T761R, The gene MUC16 has a mutation status of A643S, The gene ZNF266 has a mutation status of H385Q, The gene RFX1 has a mutation status of V786A, The gene USHBP1 has a mutation status of Y356H, The gene ZNF536 has a mutation status of Q356K, The gene APOE has a mutation status of H158N, The gene APOE has a mutation status of H158Q, The gene MYPOP has a mutation status of K330N, The gene MYPOP has a mutation status of A328T, The gene MSH6 has a mutation status of F1088LfsTer5, The gene CCDC88A has a mutation status of L1215M, The gene OTX1 has a mutation status of Q352E, The gene THNSL2 has a mutation status of R450S, The gene MAP4K4 has a mutation status of Q402R, The gene SH3RF3 has a mutation status of R179Q, The gene SLC25A12 has a mutation status of R624H, The gene NYAP2 has a mutation status of H83Q, The gene NRSN2 has a mutation status of G14V, The gene DTD1 has a mutation status of D156E, The gene RIN2 has a mutation status of L724F, The gene UBE2C has a mutation status of S87R, The gene FAM217B has a mutation status of R248L, The gene C21orf91 has a mutation status of V98M, The gene TTC28 has a mutation status of R24L, The gene SYN3 has a mutation status of Q428H, The gene HRH1 has a mutation status of M451V, The gene EAF1 has a mutation status of P26Q, The gene EOMES has a mutation status of F316L, The gene SMC4 has a mutation status of R107C, The gene TMEM129 has a mutation status of V344L, The gene TMEM129 has a mutation status of P336H, The gene CFAP99 has a mutation status of A91D, The gene HMX1 has a mutation status of R212S, The gene HMX1 has a mutation status of V209A, The gene LCORL has a mutation status of C1815Y, The gene SEL1L3 has a mutation status of V877A, The gene FAT4 has a mutation status of F4337LfsTer60, The gene IQCM has a mutation status of E17K, The gene PALLD has a mutation status of S199P, The gene CFAP97 has a mutation status of F353L, The gene NKD2 has a mutation status of P373T, The gene RICTOR has a mutation status of G407A, The gene CSNK1G3 has a mutation status of L247F, The gene MINAR2 has a mutation status of E115Q, The gene FBLL1 has a mutation status of L198M, The gene ZFP2 has a mutation status of C160Y, The gene RUFY1 has a mutation status of G135D, The gene TRIM7 has a mutation status of G9R, The gene FAM8A1 has a mutation status of G134I, The gene FAM8A1 has a mutation status of A140T, The gene H3C1 has a mutation status of D82H, The gene HLA-DRB5 has a mutation status of Q38W, The gene RHAG has a mutation status of M269I, The gene SLC22A16 has a mutation status of K530Ter, The gene TULP4 has a mutation status of V301F, The gene EPHA1 has a mutation status of R577G, The gene CLDN23 has a mutation status of E211Ter, The gene THAP1 has a mutation status of P103A, The gene CRH has a mutation status of Q39Ter, The gene RNF19A has a mutation status of Y811C, The gene KDM4C has a mutation status of N704T, The gene WNK2 has a mutation status of P1004H, The gene PTCH1 has a mutation status of G37V, The gene SUSD1 has a mutation status of S212N, The gene MT-CYB has a mutation status of A380T, The gene NLGN4X has a mutation status of R753S, The gene DCAF8L2 has a mutation status of G125V, The gene SLC25A5 has a mutation status of T221R	PRAD
The gene HNRNPCL2 has a mutation status of Q262Ter, The gene NBPF1 has a mutation status of C663H, The gene ZNF683 has a mutation status of S28I, The gene TARS2 has a mutation status of L3P, The gene SETDB1 has a mutation status of K411R, The gene FLG has a mutation status of I3191T, The gene NES has a mutation status of Q1103GfsTer38, The gene PBX1 has a mutation status of S187I, The gene PTPN14 has a mutation status of H991Q, The gene JMJD4 has a mutation status of I123T, The gene KIF5B has a mutation status of L799SfsTer73, The gene CHCHD1 has a mutation status of P115S, The gene ACTR1A has a mutation status of R182H, The gene SORCS3 has a mutation status of S187del, The gene MUC5AC has a mutation status of A5353K, The gene TRPM5 has a mutation status of P224S, The gene MYBPC3 has a mutation status of C1244_P1245delinsTer, The gene AHNAK has a mutation status of D1340V, The gene MRPL21 has a mutation status of F141V, The gene DLG2 has a mutation status of I899T, The gene TAS2R19 has a mutation status of L116F, The gene TAS2R43 has a mutation status of L193I, The gene DUSP16 has a mutation status of L499R, The gene NACA has a mutation status of P1320A, The gene PTPRB has a mutation status of L1084H, The gene DNAH10 has a mutation status of F2122LfsTer6, The gene ABCC4 has a mutation status of N823I, The gene ADPRHL1 has a mutation status of G1804_R1805insWEQTHIEAQGQAQKGAQERAREQAQKGAQERAREQG, The gene LRRC9 has a mutation status of E727Ter, The gene RPS6KA5 has a mutation status of R148H, The gene TRPM7 has a mutation status of Q789P, The gene NEDD4 has a mutation status of Y842Ter, The gene CIAO3 has a mutation status of R255I, The gene HAPSTR1 has a mutation status of R155Ter, The gene ITGAM has a mutation status of R699L, The gene CHST4 has a mutation status of H321R, The gene TP53 has a mutation status of P152RfsTer18, The gene SPDYE4 has a mutation status of V28A, The gene SP6 has a mutation status of G157EfsTer27, The gene MRC2 has a mutation status of V1048SfsTer3, The gene CSHL1 has a mutation status of T127M, The gene ENDOV has a mutation status of L87F, The gene ROCK1 has a mutation status of T9NfsTer4, The gene ELP2 has a mutation status of L279AfsTer5, The gene ADAT3 has a mutation status of P306S, The gene CAMSAP3 has a mutation status of A103V, The gene KEAP1 has a mutation status of R326H, The gene CACNA1A has a mutation status of E2069K, The gene B3GNT3 has a mutation status of A57P, The gene ECH1 has a mutation status of N79T, The gene EXOC3L2 has a mutation status of A466TfsTer35, The gene FAM90A27P has a mutation status of Q123K, The gene LENG1 has a mutation status of G143RfsTer127, The gene LILRA1 has a mutation status of P271R, The gene LILRB1 has a mutation status of Q401L, The gene ZNF324 has a mutation status of L185V, The gene GREB1 has a mutation status of E1614Q, The gene GCC2 has a mutation status of L925F, The gene C1QL2 has a mutation status of P98A, The gene SAP130 has a mutation status of P322S, The gene SAP130 has a mutation status of D314N, The gene LRP1B has a mutation status of N2074T, The gene HECW2 has a mutation status of W1528Ter, The gene SLC4A3 has a mutation status of D867P, The gene PKIG has a mutation status of G28E, The gene COL9A3 has a mutation status of G121R, The gene IFNAR2 has a mutation status of V24IfsTer24, The gene SCN5A has a mutation status of T512I, The gene CDC25A has a mutation status of T208A, The gene KLHDC8B has a mutation status of D153A, The gene GABRR3 has a mutation status of E201K, The gene KCNMB3 has a mutation status of P3A, The gene MUC4 has a mutation status of D2261_T2292del, The gene MUC4 has a mutation status of P2070V, The gene EVC2 has a mutation status of G225R, The gene FBXL5 has a mutation status of E211V, The gene CDS1 has a mutation status of F261L, The gene ASIC5 has a mutation status of S456N, The gene SLC6A18 has a mutation status of S30R, The gene ATPSCKMT has a mutation status of R217C, The gene WDR70 has a mutation status of D528H, The gene PCDHB8 has a mutation status of S397P, The gene SH3RF2 has a mutation status of S620P, The gene DRD1 has a mutation status of G174E, The gene ZNF454 has a mutation status of Q207H, The gene H1-3 has a mutation status of R130M, The gene RHAG has a mutation status of G376S, The gene L3MBTL3 has a mutation status of E338K, The gene SLC18B1 has a mutation status of R298S, The gene ARID1B has a mutation status of R19G, The gene TAX1BP1 has a mutation status of M298I, The gene FIGNL1 has a mutation status of G237A, The gene MUC3A has a mutation status of T303V, The gene MUC3A has a mutation status of G307H, The gene IQCA1L has a mutation status of R666C, The gene CSMD1 has a mutation status of S216N, The gene TRMT9B has a mutation status of E236K, The gene ASAH1 has a mutation status of P2S, The gene NKX6-3 has a mutation status of R109W, The gene TNFRSF11B has a mutation status of G127R, The gene TEK has a mutation status of H894Y, The gene UNC13B has a mutation status of L1914F, The gene SLC44A1 has a mutation status of I306V, The gene RALGDS has a mutation status of E472G, The gene MT-ND1 has a mutation status of T164A, The gene MXRA5 has a mutation status of P2174H, The gene ASB9 has a mutation status of M199V, The gene FAM47C has a mutation status of H317P, The gene MORC4 has a mutation status of Q638Ter	OV
The gene S100PBP has a mutation status of L350F, The gene NOTCH2 has a mutation status of D661E, The gene S100A10 has a mutation status of Q93H, The gene SH2D2A has a mutation status of G66E, The gene DNM3 has a mutation status of R271Q, The gene PIK3C2B has a mutation status of L1283Ter, The gene USH2A has a mutation status of L2135V, The gene HLX has a mutation status of A166V, The gene DNAH14 has a mutation status of V1848I, The gene DISC1 has a mutation status of M291T, The gene PLD5 has a mutation status of E303K, The gene OR2T12 has a mutation status of T6N, The gene KIAA1217 has a mutation status of Q1426K, The gene HKDC1 has a mutation status of Q607H, The gene INA has a mutation status of Y315H, The gene CCDC88B has a mutation status of D886S, The gene PTPRO has a mutation status of I1164F, The gene MUC19 has a mutation status of S1266N, The gene EEF1AKMT3 has a mutation status of G87C, The gene SETD1B has a mutation status of K938E, The gene NBEA has a mutation status of Y957F, The gene TRAV36DV7 has a mutation status of C44Y, The gene AKAP6 has a mutation status of A2067P, The gene RPL10L has a mutation status of W171L, The gene FOS has a mutation status of S260G, The gene LPCAT4 has a mutation status of A375V, The gene RPUSD2 has a mutation status of R275H, The gene WDR90 has a mutation status of A786V, The gene ZFHX3 has a mutation status of D3659IfsTer34, The gene TP53 has a mutation status of E271Ter, The gene NF1 has a mutation status of Q347H, The gene MYO1D has a mutation status of D167N, The gene C17orf78 has a mutation status of T169S, The gene ARHGAP23 has a mutation status of E955G, The gene RARA has a mutation status of G101TfsTer37, The gene KRTAP4-6 has a mutation status of R106H, The gene KCNH4 has a mutation status of T330A, The gene MAP3K14 has a mutation status of E767G, The gene SGCA has a mutation status of T208I, The gene SDK2 has a mutation status of A814F, The gene POLRMT has a mutation status of A777V, The gene MICOS13 has a mutation status of P68A, The gene ZNF737 has a mutation status of P521L, The gene FCGBP has a mutation status of V4112L, The gene ZNF546 has a mutation status of I322T, The gene ZNF235 has a mutation status of S311CfsTer12, The gene NTN5 has a mutation status of P462T, The gene LILRB1 has a mutation status of Q401L, The gene SSC5D has a mutation status of S1140F, The gene ZNF329 has a mutation status of L186PfsTer6, The gene KIDINS220 has a mutation status of I1237V, The gene RASGRP3 has a mutation status of H159Y, The gene VPS54 has a mutation status of M167L, The gene RNF149 has a mutation status of K277T, The gene POLR1B has a mutation status of R579P, The gene CYBRD1 has a mutation status of L81P, The gene DLX1 has a mutation status of A154P, The gene SP3 has a mutation status of S389C, The gene PLCL1 has a mutation status of Q770L, The gene KIF1A has a mutation status of L1428I, The gene EPB41L1 has a mutation status of G73S, The gene PREX1 has a mutation status of I454F, The gene ZNF217 has a mutation status of Y17F, The gene HELZ2 has a mutation status of H1783Y, The gene SON has a mutation status of V646G, The gene SBF1 has a mutation status of R1557H, The gene NGLY1 has a mutation status of N486Y, The gene QRICH1 has a mutation status of P461QfsTer9, The gene ZNF717 has a mutation status of L21_V22insISFEDVAVHFTWEEWQDLDNAQRTLYRD, The gene ZIC4 has a mutation status of Y264Ter, The gene VEPH1 has a mutation status of R782G, The gene PIK3CA has a mutation status of C420R, The gene ZNF718 has a mutation status of V88L, The gene CRACD has a mutation status of Q84K, The gene ANTXR2 has a mutation status of G136V, The gene METAP1 has a mutation status of M329V, The gene NDST3 has a mutation status of D584E, The gene ASIC5 has a mutation status of S44Y, The gene ADAM29 has a mutation status of T800M, The gene CFAP97 has a mutation status of T60A, The gene F11 has a mutation status of S495F, The gene TRIML1 has a mutation status of A293G, The gene ZSWIM6 has a mutation status of I109L, The gene ZSWIM6 has a mutation status of W112Ter, The gene PPIP5K2 has a mutation status of Q396E, The gene PCDHB11 has a mutation status of A570T, The gene PCDHB13 has a mutation status of S534T, The gene ZSCAN26 has a mutation status of D132N, The gene SLC29A1 has a mutation status of R228C, The gene SENP6 has a mutation status of E39Ter, The gene EPHA7 has a mutation status of Y365Ter, The gene MFSD4B has a mutation status of L182Y, The gene MYCT1 has a mutation status of R23I, The gene SCAF8 has a mutation status of A32YfsTer2, The gene PDE10A has a mutation status of A335T, The gene SKAP2 has a mutation status of T296I, The gene GTF2IRD1 has a mutation status of V406I, The gene TRRAP has a mutation status of A1920G, The gene EZH2 has a mutation status of P193R, The gene GOT1L1 has a mutation status of H369L, The gene MROH1 has a mutation status of E322SfsTer7, The gene ARHGAP39 has a mutation status of A550T, The gene MYORG has a mutation status of D442N, The gene TRPM6 has a mutation status of P1951S, The gene SVEP1 has a mutation status of G1028R, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene TXLNG has a mutation status of T334K, The gene CFAP47 has a mutation status of N2532D, The gene JADE3 has a mutation status of E75A, The gene ARHGEF9 has a mutation status of Y177F, The gene AMER1 has a mutation status of D233G, The gene THOC2 has a mutation status of S485N, The gene ARHGAP36 has a mutation status of A508S, The gene CD40LG has a mutation status of H125N	BRCA
The gene SAMD11 has a mutation status of A125E, The gene SAMD11 has a mutation status of R130H, The gene KLHL21 has a mutation status of R275L, The gene UBE4B has a mutation status of E1112D, The gene HSPG2 has a mutation status of P2142T, The gene KCNQ4 has a mutation status of A402G, The gene ATP1A1 has a mutation status of V329L, The gene ACP6 has a mutation status of D44Y, The gene CRNN has a mutation status of R424L, The gene RGS4 has a mutation status of G24S, The gene IGFN1 has a mutation status of G882W, The gene HHAT has a mutation status of V72GfsTer12, The gene DIP2C has a mutation status of D443A, The gene MPP7 has a mutation status of P87KfsTer4, The gene PCDH15 has a mutation status of K1023N, The gene CHUK has a mutation status of P239L, The gene HABP2 has a mutation status of Y195C, The gene SPADH has a mutation status of I41V, The gene B4GALNT4 has a mutation status of A716S, The gene MUC5B has a mutation status of A1131G, The gene OR52B4 has a mutation status of I143N, The gene ILK has a mutation status of D21G, The gene KIAA1549L has a mutation status of A2V, The gene CAPRIN1 has a mutation status of S642L, The gene C1QTNF4 has a mutation status of A192S, The gene TRIM64C has a mutation status of N367I, The gene INCENP has a mutation status of A130G, The gene INTS5 has a mutation status of G22V, The gene MRPL11 has a mutation status of D158H, The gene INPPL1 has a mutation status of G1191W, The gene FAT3 has a mutation status of G4554N, The gene DYNC2H1 has a mutation status of G2370E, The gene EXPH5 has a mutation status of L1898S, The gene PCSK7 has a mutation status of G358E, The gene KCNJ8 has a mutation status of R352W, The gene KRAS has a mutation status of G12R, The gene GXYLT1 has a mutation status of C414H, The gene FIGNL2 has a mutation status of R267H, The gene KRT80 has a mutation status of D247Y, The gene LEMD3 has a mutation status of S117G, The gene LEMD3 has a mutation status of P122T, The gene TDG has a mutation status of I137du, The gene DDX51 has a mutation status of S140R, The gene CHFR has a mutation status of R148PfsTer8, The gene WBP4 has a mutation status of D122IfsTer8, The gene TMTC4 has a mutation status of R611L, The gene AP1G2 has a mutation status of A64T, The gene PCNX4 has a mutation status of R663C, The gene ATP10A has a mutation status of R85H, The gene MAP2K1 has a mutation status of Q10K, The gene SKOR1 has a mutation status of E332K, The gene C15orf39 has a mutation status of E795K, The gene COMMD4 has a mutation status of E160G, The gene PLIN1 has a mutation status of A57V, The gene HBZ has a mutation status of T138P, The gene RGS11 has a mutation status of D90N, The gene PTX4 has a mutation status of L313PfsTer10, The gene PPL has a mutation status of K36R, The gene SEC14L5 has a mutation status of H513N, The gene EEF2KMT has a mutation status of S28Y, The gene LCAT has a mutation status of Q387PfsTer54, The gene ADAMTS18 has a mutation status of A870PfsTer28, The gene SLC38A8 has a mutation status of H232R, The gene MBTPS1 has a mutation status of S182N, The gene FBXO31 has a mutation status of A201P, The gene FBXO31 has a mutation status of K200R, The gene CPNE7 has a mutation status of P71H, The gene TRPV1 has a mutation status of N629T, The gene CHRNB1 has a mutation status of E25G, The gene ZBTB4 has a mutation status of P598R, The gene ZBTB4 has a mutation status of L595V, The gene TP53 has a mutation status of R282W, The gene SHISA6 has a mutation status of R518C, The gene BLTP2 has a mutation status of W2138L, The gene TMEM132E has a mutation status of T188A, The gene TMEM132E has a mutation status of C189S, The gene HROB has a mutation status of Y572C, The gene SLC35B1 has a mutation status of G265S, The gene NOTUM has a mutation status of A383P, The gene DLGAP1 has a mutation status of M351I, The gene ELOA2 has a mutation status of S681T, The gene MBD1 has a mutation status of H77L, The gene PCSK4 has a mutation status of P193T, The gene PNPLA6 has a mutation status of R666H, The gene PRR36 has a mutation status of A373V, The gene FDX2 has a mutation status of M1?, The gene BEST2 has a mutation status of M386R, The gene GGN has a mutation status of A537G, The gene RINL has a mutation status of P140S, The gene RABAC1 has a mutation status of V68L, The gene GSK3A has a mutation status of G325W, The gene TOMM40 has a mutation status of N79H, The gene ZC3H4 has a mutation status of P862T, The gene HRC has a mutation status of W14C, The gene TBC1D17 has a mutation status of A163P, The gene EMC10 has a mutation status of V162E, The gene BRSK1 has a mutation status of P25H, The gene C2orf16 has a mutation status of C1412Y, The gene NAT8B has a mutation status of K15QfsTer82, The gene SCN2A has a mutation status of N1196K, The gene COL3A1 has a mutation status of G1050D, The gene TNS1 has a mutation status of Q791Ter, The gene WNT6 has a mutation status of G229Ter, The gene SPEG has a mutation status of T2051A, The gene SPEG has a mutation status of L2352R, The gene OBSL1 has a mutation status of Q1809P, The gene OBSL1 has a mutation status of L1806F, The gene RBM44 has a mutation status of T944A, The gene STK25 has a mutation status of N9S, The gene SIGLEC1 has a mutation status of L992Q, The gene SIGLEC1 has a mutation status of L989H, The gene SLC24A3 has a mutation status of A31V, The gene RALGAPA2 has a mutation status of K11M, The gene SSTR4 has a mutation status of F275L, The gene LAMA5 has a mutation status of E2031Q, The gene KCNQ2 has a mutation status of C429Y, The gene RSPH1 has a mutation status of A253D, The gene XKR3 has a mutation status of C45Y, The gene ARFGAP3 has a mutation status of S451A, The gene MAPK8IP2 has a mutation status of A544G, The gene SHANK3 has a mutation status of L98_T99delinsFA, The gene LRRC2 has a mutation status of K364N, The gene TMEM115 has a mutation status of S320R, The gene ERC2 has a mutation status of N53S, The gene DENND6A has a mutation status of G37C, The gene NXPE3 has a mutation status of A279D, The gene MSL2 has a mutation status of P425R, The gene PAQR9 has a mutation status of Y278P, The gene MUC4 has a mutation status of V3305_S3336del, The gene MUC4 has a mutation status of D2979_P3010del, The gene KCTD8 has a mutation status of P262A, The gene BLTP1 has a mutation status of T4589_S4598del, The gene IQCM has a mutation status of K316E, The gene CPE has a mutation status of A226D, The gene DDX60L has a mutation status of T1141A, The gene NIPBL has a mutation status of E1532delinsDK, The gene IRF1 has a mutation status of P145S, The gene SFXN1 has a mutation status of I191V, The gene TMED9 has a mutation status of A32G, The gene SLC22A23 has a mutation status of G491W, The gene IER3 has a mutation status of S62N, The gene FANCE has a mutation status of R134H, The gene PKHD1 has a mutation status of G604V, The gene GABRR2 has a mutation status of R354C, The gene STXBP5 has a mutation status of S17L, The gene GET4 has a mutation status of S55VfsTer48, The gene PHF14 has a mutation status of S296I, The gene MUC3A has a mutation status of T1379P, The gene KCP has a mutation status of A226P, The gene ZNF467 has a mutation status of R224H, The gene ZNF467 has a mutation status of C218Y, The gene ZNF775 has a mutation status of H341Y, The gene LMBR1 has a mutation status of C202Y, The gene TNKS has a mutation status of H12N, The gene PTK2B has a mutation status of P645A, The gene KIF13B has a mutation status of A1605V, The gene TSPYL5 has a mutation status of E184G, The gene MTSS1 has a mutation status of C103R, The gene TJP2 has a mutation status of A647S, The gene TRPM6 has a mutation status of E1638GfsTer12, The gene FOXB2 has a mutation status of A224V, The gene ELP1 has a mutation status of F631L, The gene DENND1A has a mutation status of Q589PfsTer44, The gene HMCN2 has a mutation status of A3931D, The gene RNF224 has a mutation status of G144A, The gene MT-ND4 has a mutation status of V313I, The gene MAGEB17 has a mutation status of G20C, The gene NHS has a mutation status of R1505Q, The gene CFP has a mutation status of Q365H, The gene ZXDB has a mutation status of E248W, The gene GJB1 has a mutation status of Y171S, The gene GRIA3 has a mutation status of V75I, The gene OR13H1 has a mutation status of C188Y	PAAD
The gene PADI6 has a mutation status of R221SfsTer13, The gene CC2D1B has a mutation status of Q750H, The gene CC2D1B has a mutation status of Q750K, The gene NRAS has a mutation status of Q61K, The gene NBPF12 has a mutation status of I17T, The gene FLG has a mutation status of Q2551E, The gene ASH1L has a mutation status of Q472H, The gene CEP350 has a mutation status of R171P, The gene WDR26 has a mutation status of K381E, The gene EPHX1 has a mutation status of E453AfsTer30, The gene PCNX2 has a mutation status of D1425E, The gene HNRNPU has a mutation status of S817N, The gene UBE2D1 has a mutation status of S83N, The gene CDHR1 has a mutation status of V121A, The gene OPN4 has a mutation status of I405V, The gene MUC6 has a mutation status of A1593P, The gene AGBL2 has a mutation status of T401N, The gene PTPRJ has a mutation status of V908A, The gene ZP1 has a mutation status of V287F, The gene MUS81 has a mutation status of P534T, The gene C11orf24 has a mutation status of A136S, The gene FGF19 has a mutation status of E174V, The gene SLC36A4 has a mutation status of A268V, The gene FOXR1 has a mutation status of R260H, The gene OR6X1 has a mutation status of M57I, The gene SCNN1A has a mutation status of R181W, The gene MON2 has a mutation status of A1494V, The gene TCHP has a mutation status of N110Y, The gene MAGEL2 has a mutation status of G1098R, The gene TJP1 has a mutation status of S747Y, The gene CAPN3 has a mutation status of K211R, The gene CX3CL1 has a mutation status of Q227K, The gene NCBP3 has a mutation status of D185N, The gene SLFN11 has a mutation status of R647Ter, The gene KRT31 has a mutation status of S55I, The gene ERN1 has a mutation status of A305S, The gene WIPI1 has a mutation status of G53R, The gene SOX9 has a mutation status of E63V, The gene LOXHD1 has a mutation status of G103C, The gene PTBP1 has a mutation status of P336_A338du, The gene MUC16 has a mutation status of H12873R, The gene FAM187B has a mutation status of R153C, The gene SIGLEC12 has a mutation status of G480A, The gene MYT1L has a mutation status of M448T, The gene EVA1A has a mutation status of G68R, The gene NCKAP5 has a mutation status of G317S, The gene TTN has a mutation status of T4686K, The gene GDF5 has a mutation status of L309M, The gene CEP250 has a mutation status of E1500K, The gene RALGAPB has a mutation status of L656M, The gene PREX1 has a mutation status of R23W, The gene PCNT has a mutation status of R1903F, The gene GAB4 has a mutation status of Q155K, The gene GSC2 has a mutation status of H129R, The gene ZNF280B has a mutation status of D113_I116delinsV, The gene SEZ6L has a mutation status of L302SfsTer11, The gene SSTR3 has a mutation status of S171L, The gene ARHGAP31 has a mutation status of E586D, The gene ARHGAP31 has a mutation status of E1223G, The gene GOLGB1 has a mutation status of E947D, The gene MCM2 has a mutation status of A112T, The gene HLTF has a mutation status of Y19D, The gene NPNT has a mutation status of G353Ter, The gene DDX60 has a mutation status of D716Y, The gene SV2C has a mutation status of E80RfsTer20, The gene PCDHGC4 has a mutation status of H770N, The gene FAT2 has a mutation status of D2950E, The gene ZNF346 has a mutation status of D184E, The gene MED23 has a mutation status of Q740Ter, The gene STEAP1B has a mutation status of Y219C, The gene HOXA4 has a mutation status of H309TfsTer45, The gene SUGCT has a mutation status of L314P, The gene PCLO has a mutation status of P2420_P2430del, The gene GRM3 has a mutation status of E111G, The gene MUC3A has a mutation status of W18G, The gene CYP7B1 has a mutation status of A26V, The gene WWP1 has a mutation status of V417F, The gene DNAJA1 has a mutation status of G121A, The gene TJP2 has a mutation status of A1023F, The gene MT-CYB has a mutation status of H16R, The gene MT-CYB has a mutation status of T158A, The gene SHOX has a mutation status of P245L, The gene VCX3B has a mutation status of Ter247YextTer13, The gene RTL9 has a mutation status of V1164M	SARC
The gene PLCH2 has a mutation status of R241H, The gene ARHGEF16 has a mutation status of E291K, The gene AJAP1 has a mutation status of L297V, The gene NPPA has a mutation status of G71E, The gene NECAP2 has a mutation status of L37W, The gene P3H1 has a mutation status of R74P, The gene USP24 has a mutation status of E1955K, The gene AGL has a mutation status of L1417RfsTer4, The gene CELSR2 has a mutation status of R2015K, The gene DCAF6 has a mutation status of V112E, The gene MYBPH has a mutation status of Q53HfsTer4, The gene CNIH3 has a mutation status of L93M, The gene OBSCN has a mutation status of L717M, The gene DHTKD1 has a mutation status of Q320Ter, The gene SRGN has a mutation status of F129L, The gene VSIR has a mutation status of S235R, The gene MCU has a mutation status of Y289H, The gene ZNF503 has a mutation status of S2T, The gene MYOF has a mutation status of K2055R, The gene SLIT1 has a mutation status of T978P, The gene PPRC1 has a mutation status of R1288L, The gene WBP1L has a mutation status of E226G, The gene CPXM2 has a mutation status of E44D, The gene CFAP46 has a mutation status of H223Q, The gene ZNF511 has a mutation status of A31G, The gene KCNQ1 has a mutation status of F127L, The gene TPP1 has a mutation status of H298N, The gene FJX1 has a mutation status of G381R, The gene FJX1 has a mutation status of Q382H, The gene MADD has a mutation status of I673T, The gene B3GAT3 has a mutation status of L10V, The gene B4GAT1 has a mutation status of A23T, The gene TBX10 has a mutation status of S274R, The gene RNF169 has a mutation status of L601M, The gene DYNC2H1 has a mutation status of G967A, The gene NXPE1 has a mutation status of D417H, The gene APLP2 has a mutation status of T4N, The gene ADAMTS15 has a mutation status of P45SfsTer38, The gene ADAMTS15 has a mutation status of D169Y, The gene MANSC4 has a mutation status of M167I, The gene MUC19 has a mutation status of N6618_I6619delinsSV, The gene CERS5 has a mutation status of P24T, The gene TAMALIN has a mutation status of L78M, The gene KRT77 has a mutation status of L431_E432insSLLSSW, The gene DAO has a mutation status of A49G, The gene SLC15A4 has a mutation status of D314N, The gene SLITRK5 has a mutation status of R343H, The gene ERCC5 has a mutation status of E1106V, The gene C13orf46 has a mutation status of G130Ter, The gene PABPN1 has a mutation status of L230WfsTer3, The gene CNIH1 has a mutation status of F3L, The gene SLC8A3 has a mutation status of V243M, The gene RIN3 has a mutation status of T830S, The gene INF2 has a mutation status of N375K, The gene ATP10A has a mutation status of D534N, The gene MEGF11 has a mutation status of P188T, The gene NPTN has a mutation status of A198V, The gene C15orf39 has a mutation status of A730T, The gene PSTPIP1 has a mutation status of T68S, The gene ANKRD34C has a mutation status of L423P, The gene BTBD1 has a mutation status of A8S, The gene AKAP13 has a mutation status of A1258G, The gene FURIN has a mutation status of P266A, The gene FURIN has a mutation status of A267D, The gene C1QTNF8 has a mutation status of A81H, The gene EMP2 has a mutation status of A66T, The gene NUBP1 has a mutation status of C8Ter, The gene TXNDC11 has a mutation status of A689G, The gene FBRS has a mutation status of A733D, The gene SMPD3 has a mutation status of L640PfsTer5, The gene SHPK has a mutation status of R23G, The gene SLC16A13 has a mutation status of S164R, The gene TP53 has a mutation status of R273H, The gene MAP2K3 has a mutation status of G76V, The gene NOS2 has a mutation status of S81Y, The gene C17orf75 has a mutation status of S35P, The gene MRM1 has a mutation status of V149P, The gene SRCIN1 has a mutation status of P707Q, The gene KRTAP16-1 has a mutation status of V323A, The gene C17orf113 has a mutation status of A407S, The gene C17orf113 has a mutation status of H402L, The gene GHDC has a mutation status of A357P, The gene TBX2 has a mutation status of P4Q, The gene TBX2 has a mutation status of A12D, The gene DDX5 has a mutation status of S2L, The gene PRKAR1A has a mutation status of E291Ter, The gene CD300H has a mutation status of I187V, The gene DLGAP1 has a mutation status of N264T, The gene LOXHD1 has a mutation status of V1147G, The gene PALM has a mutation status of L84Q, The gene GRIN3B has a mutation status of A917D, The gene PLEKHJ1 has a mutation status of E101G, The gene ADAMTS10 has a mutation status of P770R, The gene PDE4A has a mutation status of A471G, The gene ZSWIM4 has a mutation status of P132S, The gene JAK3 has a mutation status of V619A, The gene CAPN12 has a mutation status of R433P, The gene LTBP4 has a mutation status of E1138G, The gene FBXO46 has a mutation status of L467V, The gene SIX5 has a mutation status of T564P, The gene PLEKHA4 has a mutation status of G642V, The gene KASH5 has a mutation status of Q157K, The gene KLK6 has a mutation status of H95P, The gene TMEM238 has a mutation status of A29G, The gene TMEM238 has a mutation status of P27L, The gene ZNF154 has a mutation status of A3S, The gene ALK has a mutation status of R41G, The gene SULT6B1 has a mutation status of G163S, The gene PLEKHH2 has a mutation status of Q1017L, The gene TET3 has a mutation status of P728L, The gene TMEM131 has a mutation status of A1779SfsTer16, The gene CLASP1 has a mutation status of E1429G, The gene AMER3 has a mutation status of V849G, The gene PLA2R1 has a mutation status of S1071Ter, The gene IGFBP5 has a mutation status of G54A, The gene IGFBP5 has a mutation status of C53Ter, The gene RNPEPL1 has a mutation status of A406D, The gene PASK has a mutation status of G117W, The gene BOK has a mutation status of V69L, The gene BOK has a mutation status of G74C, The gene DDRGK1 has a mutation status of E136Ter, The gene MCM8 has a mutation status of L387HfsTer41, The gene XKR7 has a mutation status of P157T, The gene CCM2L has a mutation status of E492D, The gene CCM2L has a mutation status of G494D, The gene GDAP1L1 has a mutation status of I65D, The gene ADA has a mutation status of V178L, The gene ARFGEF2 has a mutation status of S1337Y, The gene SLCO4A1 has a mutation status of D647G, The gene ADAMTS5 has a mutation status of A65E, The gene PKNOX1 has a mutation status of D52N, The gene PFKL has a mutation status of F229V, The gene RASL10A has a mutation status of G118V, The gene MCM5 has a mutation status of D601A, The gene SGSM3 has a mutation status of S677R, The gene TUBGCP6 has a mutation status of L1321M, The gene SHANK3 has a mutation status of E768G, The gene SHANK3 has a mutation status of A772V, The gene EDEM1 has a mutation status of D153E, The gene EDEM1 has a mutation status of N156H, The gene NR2C2 has a mutation status of R402Q, The gene GLB1 has a mutation status of A594T, The gene ITGA9 has a mutation status of M777V, The gene PLXNB1 has a mutation status of W16Ter, The gene CACNA1D has a mutation status of R1525M, The gene MAGI1 has a mutation status of Q1238K, The gene OR5K1 has a mutation status of G233Ter, The gene SPICE1 has a mutation status of N147K, The gene ATP6V1A has a mutation status of A37G, The gene ZIC1 has a mutation status of A19E, The gene SLC26A1 has a mutation status of G316C, The gene FGFR3 has a mutation status of E194G, The gene FGFR3 has a mutation status of F195V, The gene CHIC2 has a mutation status of Q21K, The gene COX18 has a mutation status of D22P, The gene SHROOM3 has a mutation status of P979Q, The gene DSPP has a mutation status of S1269R, The gene PRDM5 has a mutation status of M326V, The gene PDGFC has a mutation status of R217K, The gene CTNND2 has a mutation status of P304T, The gene CTNND2 has a mutation status of S303W, The gene NPR3 has a mutation status of A159G, The gene LIFR has a mutation status of G818L, The gene FYB1 has a mutation status of G230E, The gene BDP1 has a mutation status of H2379Y, The gene ARSB has a mutation status of S96R, The gene ARSB has a mutation status of R95G, The gene HAPLN1 has a mutation status of Y348C, The gene MCTP1 has a mutation status of A22P, The gene MCTP1 has a mutation status of F20C, The gene SLC22A5 has a mutation status of W62C, The gene DND1 has a mutation status of Q112R, The gene PCDHA10 has a mutation status of F190V, The gene LARP1 has a mutation status of S75R, The gene WWC1 has a mutation status of E830G, The gene TRIM26 has a mutation status of T3M, The gene HLA-C has a mutation status of S140L, The gene HLA-B has a mutation status of Y140L, The gene HLA-DRB1 has a mutation status of S66N, The gene TAP2 has a mutation status of I659V, The gene TAP2 has a mutation status of V467I, The gene COL11A2 has a mutation status of R151H, The gene LEMD2 has a mutation status of G116W, The gene KCNK16 has a mutation status of A248G, The gene TMEM151B has a mutation status of P3T, The gene ZNF451 has a mutation status of H277Y, The gene CASP8AP2 has a mutation status of S1721N, The gene SOGA3 has a mutation status of A298P, The gene HIVEP2 has a mutation status of S629C, The gene GRM1 has a mutation status of S317I, The gene DNAAF5 has a mutation status of G531C, The gene LFNG has a mutation status of Y295Ter, The gene CAMK2B has a mutation status of D404G, The gene STYXL1 has a mutation status of Y138C, The gene TECPR1 has a mutation status of V226A, The gene MUC3A has a mutation status of V1672D, The gene NAT16 has a mutation status of G239V, The gene BRAF has a mutation status of P490YfsTer11, The gene BRAF has a mutation status of L485YfsTer14, The gene TRBV13 has a mutation status of T47P, The gene KRBA1 has a mutation status of Y347Ter, The gene SOX7 has a mutation status of R117L, The gene ZNF395 has a mutation status of E352K, The gene FZD6 has a mutation status of Q464E, The gene CSMD3 has a mutation status of G3469R, The gene JRK has a mutation status of C405S, The gene FAM83H has a mutation status of P560T, The gene SLC39A4 has a mutation status of E480Ter, The gene SLC39A4 has a mutation status of V384L, The gene RECQL4 has a mutation status of E936G, The gene NR5A1 has a mutation status of K150R, The gene HMCN2 has a mutation status of P1687R, The gene NACC2 has a mutation status of Y330Ter, The gene CCDC22 has a mutation status of S446A, The gene AWAT1 has a mutation status of E95Ter, The gene RAB40A has a mutation status of P137A, The gene SLC25A53 has a mutation status of V236A, The gene RBMXL3 has a mutation status of W317C, The gene SLC25A5 has a mutation status of T221R	LUAD
The gene DISP3 has a mutation status of G491R, The gene PRAMEF20 has a mutation status of R4P, The gene ARID1A has a mutation status of G272V, The gene DNAJC6 has a mutation status of G307V, The gene GATAD2B has a mutation status of R264C, The gene OR6Y1 has a mutation status of P267A, The gene ITLN1 has a mutation status of Y223C, The gene ODR4 has a mutation status of D156N, The gene C1orf116 has a mutation status of T254A, The gene USH2A has a mutation status of E5070K, The gene RYR2 has a mutation status of G2945A, The gene ARHGAP21 has a mutation status of R1296G, The gene ASCC1 has a mutation status of H109R, The gene PDZD8 has a mutation status of F304Y, The gene LRP4 has a mutation status of Y1792C, The gene LRP4 has a mutation status of E856D, The gene TRIM64C has a mutation status of A253E, The gene NRXN2 has a mutation status of P684H, The gene NOX4 has a mutation status of T541QfsTer19, The gene UBE4A has a mutation status of A802T, The gene MUC19 has a mutation status of S6854L, The gene PUS7L has a mutation status of I301M, The gene KSR2 has a mutation status of P537L, The gene MPHOSPH8 has a mutation status of L441I, The gene ERICH6B has a mutation status of E138V, The gene ERICH6B has a mutation status of E135G, The gene CUL4A has a mutation status of D3E, The gene CFL2 has a mutation status of K127R, The gene TOGARAM1 has a mutation status of T64I, The gene FERMT2 has a mutation status of M316QfsTer13, The gene TBPL2 has a mutation status of Ter344GextTer12, The gene ASB2 has a mutation status of D562G, The gene IGHG3 has a mutation status of S370N, The gene TYRO3 has a mutation status of K235AfsTer18, The gene FBN1 has a mutation status of H1877R, The gene GTF3C1 has a mutation status of E623G, The gene KAT8 has a mutation status of W192C, The gene MBTPS1 has a mutation status of L930F, The gene TP53 has a mutation status of R213Ter, The gene ELOA2 has a mutation status of P189S, The gene ZNF407 has a mutation status of M2I, The gene KISS1R has a mutation status of G26A, The gene SBNO2 has a mutation status of P1347S, The gene SEMA6B has a mutation status of A673S, The gene MCOLN1 has a mutation status of G112R, The gene MUC16 has a mutation status of S9145P, The gene CYP2A6 has a mutation status of E419K, The gene ZNF283 has a mutation status of E2V, The gene NLRP8 has a mutation status of V632A, The gene LPIN1 has a mutation status of R665W, The gene RDH14 has a mutation status of Q86H, The gene CRIPT has a mutation status of G69R, The gene ITGA6 has a mutation status of F276LfsTer17, The gene TTN has a mutation status of E13365Ter, The gene C2CD6 has a mutation status of H1762N, The gene KIAA2012 has a mutation status of Q266Ter, The gene NEU4 has a mutation status of S45N, The gene EIF6 has a mutation status of A103T, The gene FAM246C has a mutation status of R158S, The gene IGLV5-45 has a mutation status of S38_L39delinsRF, The gene IGLV5-45 has a mutation status of A95T, The gene IGLV5-45 has a mutation status of I99L, The gene C1QTNF6 has a mutation status of H81Y, The gene TRANK1 has a mutation status of S2711F, The gene FYCO1 has a mutation status of G1385A, The gene CCDC66 has a mutation status of K264N, The gene SLIT2 has a mutation status of Q483E, The gene FAT4 has a mutation status of G3016Ter, The gene BDP1 has a mutation status of P2381L, The gene IQGAP2 has a mutation status of L687V, The gene EDIL3 has a mutation status of G313R, The gene RAD50 has a mutation status of D967V, The gene GABRA6 has a mutation status of S71_D72insKY, The gene GABRA6 has a mutation status of D72AfsTer3, The gene TFAP2D has a mutation status of M156R, The gene TNFAIP3 has a mutation status of Q784K, The gene UTRN has a mutation status of E1160Q, The gene TPST1 has a mutation status of D185G, The gene STEAP4 has a mutation status of G387R, The gene SPACDR has a mutation status of W123R, The gene MUC3A has a mutation status of N2136_E2152del, The gene WNT2 has a mutation status of L15F, The gene CTTNBP2 has a mutation status of S1005T, The gene KCP has a mutation status of R136S, The gene KAT6A has a mutation status of S510C, The gene DEPTOR has a mutation status of H56QfsTer14, The gene SQLE has a mutation status of F78Y, The gene FRMD3 has a mutation status of E218Ter, The gene ROR2 has a mutation status of K489N, The gene ZNF782 has a mutation status of Q11H, The gene FCN2 has a mutation status of K268_N269del, The gene MT-ND4 has a mutation status of G239V, The gene MT-ND4 has a mutation status of G240C, The gene MT-CYB has a mutation status of I27T, The gene ASB11 has a mutation status of A277T, The gene ARAF has a mutation status of A475P, The gene ATP7A has a mutation status of S1473F, The gene HDX has a mutation status of N414K, The gene MID2 has a mutation status of C688R, The gene SLC6A8 has a mutation status of R278P	DLBC
The gene RPS6KA1 has a mutation status of P393A, The gene ARID1A has a mutation status of G1255E, The gene SFPQ has a mutation status of Q70H, The gene NEGR1 has a mutation status of P89L, The gene TGFBR3 has a mutation status of G798R, The gene PHTF1 has a mutation status of G173E, The gene ITGA10 has a mutation status of G922R, The gene H2AC21 has a mutation status of D91E, The gene MAEL has a mutation status of I114N, The gene RNF2 has a mutation status of G35D, The gene LHX9 has a mutation status of T43P, The gene CHRM3 has a mutation status of A72T, The gene ITGA8 has a mutation status of H562N, The gene TMEM236 has a mutation status of Ter352YextTer6, The gene MARCHF8 has a mutation status of A251G, The gene CDH23 has a mutation status of R27Q, The gene PLCE1 has a mutation status of E2255DfsTer22, The gene SLIT1 has a mutation status of A754S, The gene TACC2 has a mutation status of G2532D, The gene CPXM2 has a mutation status of L401M, The gene CEND1 has a mutation status of K6N, The gene MUC5AC has a mutation status of Q718E, The gene OR52E5 has a mutation status of A66G, The gene OVCH2 has a mutation status of S387R, The gene PLEKHA7 has a mutation status of F698I, The gene CD5 has a mutation status of H461C, The gene CPSF7 has a mutation status of P210R, The gene KDM4D has a mutation status of Q77H, The gene PRH1 has a mutation status of P163L, The gene MUC19 has a mutation status of I6366K, The gene ITGA7 has a mutation status of E25G, The gene MON2 has a mutation status of R1221S, The gene NAA25 has a mutation status of S226C, The gene HSPB8 has a mutation status of E84D, The gene TMEM132C has a mutation status of L599Q, The gene CDK8 has a mutation status of P232Q, The gene CLDN10 has a mutation status of P149R, The gene TTC6 has a mutation status of E252D, The gene SYT16 has a mutation status of Q635L, The gene SMOC1 has a mutation status of A234T, The gene EXOC3L4 has a mutation status of F576SfsTer11, The gene PLA2G4F has a mutation status of L505S, The gene DPP8 has a mutation status of K801M, The gene WHAMM has a mutation status of W78C, The gene WDR73 has a mutation status of S24Ter, The gene RAB11FIP3 has a mutation status of D56N, The gene SRRM2 has a mutation status of D1141V, The gene GREP1 has a mutation status of G200A, The gene SHISA9 has a mutation status of G43R, The gene CEP20 has a mutation status of A112T, The gene FBRS has a mutation status of A387G, The gene ASGR2 has a mutation status of Q47Ter, The gene MYH3 has a mutation status of Y1853C, The gene MPRIP has a mutation status of E143Q, The gene MYO19 has a mutation status of I168V, The gene PLEKHM1 has a mutation status of R628G, The gene KANSL1 has a mutation status of S847Y, The gene PITPNC1 has a mutation status of V193I, The gene TMEM104 has a mutation status of F384PfsTer139, The gene KDM4B has a mutation status of P527L, The gene PODNL1 has a mutation status of E493D, The gene ZNF507 has a mutation status of V305D, The gene ZNF229 has a mutation status of L308P, The gene NOSIP has a mutation status of G189V, The gene SPACA6 has a mutation status of M167T, The gene KIF5C has a mutation status of S622G, The gene KIF5C has a mutation status of S681G, The gene COL3A1 has a mutation status of Q1127H, The gene MARS2 has a mutation status of G570R, The gene C2orf72 has a mutation status of G276W, The gene RALGAPA2 has a mutation status of H1752R, The gene NRIP1 has a mutation status of S972I, The gene PCNT has a mutation status of Q1588Ter, The gene CLTCL1 has a mutation status of N653S, The gene MYH9 has a mutation status of Y106C, The gene CACNA1D has a mutation status of P1912L, The gene ERC2 has a mutation status of S340N, The gene POLQ has a mutation status of G1871D, The gene CCDC14 has a mutation status of H165Y, The gene LRRC31 has a mutation status of E173G, The gene MUC4 has a mutation status of E2741_T2742delinsDA, The gene FBXO45 has a mutation status of N219S, The gene C9 has a mutation status of P56H, The gene MAN2A1 has a mutation status of S1081I, The gene PCDHGA4 has a mutation status of A230VfsTer2, The gene HMGXB3 has a mutation status of H1013R, The gene SYNPO has a mutation status of I114T, The gene SLC34A1 has a mutation status of W576Ter, The gene PPP1R3G has a mutation status of R353C, The gene HLA-C has a mutation status of S140L, The gene RAB44 has a mutation status of V988L, The gene DNAH8 has a mutation status of G3442R, The gene PRPH2 has a mutation status of D338G, The gene SAMD3 has a mutation status of R89L, The gene PLG has a mutation status of P159T, The gene EIF3B has a mutation status of L711P, The gene ELMO1 has a mutation status of D382H, The gene GJC3 has a mutation status of L71I, The gene MUC3A has a mutation status of V43A, The gene MUC3A has a mutation status of L58Q, The gene PARP12 has a mutation status of D657N, The gene TRBD1 has a mutation status of G4V, The gene SHH has a mutation status of R232L, The gene RP1L1 has a mutation status of W548Ter, The gene RP1L1 has a mutation status of A138T, The gene CHRNA2 has a mutation status of S42Y, The gene GOLGA7 has a mutation status of Q100R, The gene PXDNL has a mutation status of P990L, The gene ZBTB10 has a mutation status of E864K, The gene SLC7A13 has a mutation status of I211F, The gene SLC7A13 has a mutation status of G106E, The gene PLEC has a mutation status of A2410L, The gene TUSC1 has a mutation status of G34S, The gene FBXO10 has a mutation status of R687Ter, The gene ZNF782 has a mutation status of G309V, The gene LCN15 has a mutation status of D165Y, The gene MT-ND5 has a mutation status of Y159H, The gene HUWE1 has a mutation status of V3984F, The gene DIAPH2 has a mutation status of E1052V, The gene THOC2 has a mutation status of S53P, The gene BCORL1 has a mutation status of P482L, The gene PLXNB3 has a mutation status of D1908N	OV
The gene EIF4G3 has a mutation status of D1218V, The gene ARID1A has a mutation status of L818CfsTer15, The gene ADGRB2 has a mutation status of E470Ter, The gene LDLRAD1 has a mutation status of A51S, The gene C1orf146 has a mutation status of N45T, The gene NRAS has a mutation status of Q61K, The gene KCNN3 has a mutation status of L66Q, The gene KCNN3 has a mutation status of P63Q, The gene SELL has a mutation status of C316F, The gene FMO3 has a mutation status of C197Y, The gene ARMC3 has a mutation status of T420A, The gene ANKRD30A has a mutation status of K1017I, The gene NLRP14 has a mutation status of R159K, The gene PPFIBP2 has a mutation status of L13M, The gene MTCH2 has a mutation status of G11D, The gene MTCH2 has a mutation status of V8M, The gene OR4C11 has a mutation status of K231N, The gene OR10W1 has a mutation status of Q149K, The gene MYO7A has a mutation status of P1671S, The gene TMPRSS13 has a mutation status of L312SfsTer8, The gene PHLDB1 has a mutation status of L352R, The gene B4GALNT3 has a mutation status of T153A, The gene CD9 has a mutation status of F124V, The gene TPI1 has a mutation status of G138_I139insK, The gene KMT2D has a mutation status of S2597AfsTer94, The gene KMT2D has a mutation status of M1379VfsTer52, The gene ANKRD52 has a mutation status of T631A, The gene KDM2B has a mutation status of P1020S, The gene EP400 has a mutation status of P2040L, The gene F7 has a mutation status of L127V, The gene GRK1 has a mutation status of L83Q, The gene MDGA2 has a mutation status of G351V, The gene NRDE2 has a mutation status of M339V, The gene AHNAK2 has a mutation status of N2143D, The gene IGHJ5 has a mutation status of S15L, The gene KNL1 has a mutation status of L1891V, The gene LTK has a mutation status of Q285L, The gene TYRO3 has a mutation status of V233HfsTer11, The gene TGM7 has a mutation status of G277A, The gene CREBBP has a mutation status of D1435E, The gene SMG1 has a mutation status of A1817T, The gene FHOD1 has a mutation status of R949H, The gene ZSWIM7 has a mutation status of A17V, The gene SLFN5 has a mutation status of F456L, The gene EVPL has a mutation status of M46I, The gene RNF125 has a mutation status of S12P, The gene BCL2 has a mutation status of A42V, The gene PRX has a mutation status of L867PfsTer50, The gene ATP1A3 has a mutation status of M31V, The gene LMTK3 has a mutation status of A381V, The gene GPN1 has a mutation status of D333E, The gene ATL2 has a mutation status of R104H, The gene EIF2AK3 has a mutation status of A51VfsTer22, The gene EIF2AK3 has a mutation status of A50D, The gene AMER3 has a mutation status of L342R, The gene ZEB2 has a mutation status of P1118H, The gene TTN has a mutation status of V33706F, The gene TTN has a mutation status of D30519Y, The gene ABCA12 has a mutation status of M1074V, The gene CUL3 has a mutation status of D698G, The gene BPIFB3 has a mutation status of S141L, The gene PIGU has a mutation status of V344CfsTer9, The gene SLA2 has a mutation status of P114A, The gene KRTAP19-5 has a mutation status of S57G, The gene SHISA8 has a mutation status of V395F, The gene PLCD1 has a mutation status of V75L, The gene CCDC13 has a mutation status of S649C, The gene CD200R1 has a mutation status of H346P, The gene BOC has a mutation status of Q331K, The gene GAP43 has a mutation status of G116D, The gene GOLGB1 has a mutation status of H1366R, The gene H1-8 has a mutation status of R215K, The gene SLC9A9 has a mutation status of P482R, The gene HTRA3 has a mutation status of T96N, The gene HTRA3 has a mutation status of C101F, The gene PROM1 has a mutation status of R712SfsTer3, The gene SDHA has a mutation status of Y205Ter, The gene RICTOR has a mutation status of N1166K, The gene NNT has a mutation status of E849Q, The gene ADGRV1 has a mutation status of S2089R, The gene SRP19 has a mutation status of S69C, The gene TRPC7 has a mutation status of A607D, The gene LRRTM2 has a mutation status of R175H, The gene PCDHGA12 has a mutation status of G795C, The gene SH3TC2 has a mutation status of A468F, The gene SYNPO has a mutation status of S153R, The gene HLA-DMB has a mutation status of M61V, The gene CILK1 has a mutation status of L48F, The gene GCM1 has a mutation status of R272Ter, The gene PHIP has a mutation status of Y16Ter, The gene FRMD1 has a mutation status of C513F, The gene GPER1 has a mutation status of E218P, The gene DAGLB has a mutation status of G322R, The gene MUC3A has a mutation status of T1234A, The gene KCND2 has a mutation status of T280A, The gene TPK1 has a mutation status of G212R, The gene ZNF783 has a mutation status of R407Q, The gene LGI3 has a mutation status of F315L, The gene MT-ND5 has a mutation status of S574P, The gene COL4A5 has a mutation status of G542R, The gene IL13RA2 has a mutation status of Y12H, The gene TENM1 has a mutation status of A437S, The gene DCAF12L1 has a mutation status of A279V, The gene MAGEC1 has a mutation status of R954C, The gene FMR1 has a mutation status of K299Q	DLBC