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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