ZBTB3
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA116251974762519747+Missense_MutationSNPCCTTCGA-FD-A62N-01A-11D-A30E-08TCGA-FD-A62N-10A-01D-A30H-08g.chr11:62519747C>Tc.1540G>Ac.(1540-1542)Gac>Aacp.D514N
BLCA116251988262519882+Missense_MutationSNPCCTTCGA-G2-AA3C-01A-21D-A391-08TCGA-G2-AA3C-10A-01D-A394-08g.chr11:62519882C>Tc.1405G>Ac.(1405-1407)Gag>Aagp.E469K
BLCA116251990962519909+Missense_MutationSNPCCATCGA-DK-A1AC-01A-11D-A13W-08TCGA-DK-A1AC-10A-01D-A13W-08g.chr11:62519909C>Ac.1378G>Tc.(1378-1380)Gct>Tctp.A460S
BLCA116252086762520867+SilentSNPCCTTCGA-UY-A9PF-01A-11D-A38G-08TCGA-UY-A9PF-10A-01D-A38J-08g.chr11:62520867C>Tc.420G>Ac.(418-420)ctG>ctAp.L140L
BLCA116252102262521022+Missense_MutationSNPGGCTCGA-BT-A3PK-01A-21D-A21Z-08TCGA-BT-A3PK-10A-01D-A21Z-08g.chr11:62521022G>Cc.265C>Gc.(265-267)Cgg>Gggp.R89G
BLCA116252149762521497+Missense_MutationSNPGGATCGA-BT-A20R-01A-12D-A16O-08TCGA-BT-A20R-11A-11D-A16O-08g.chr11:62521497G>Ac.38C>Tc.(37-39)tCg>tTgp.S13L
BRCA116252058462520584+Missense_MutationSNPCCTTCGA-E2-A10B-01A-11D-A10M-09TCGA-E2-A10B-10A-01D-A10M-09g.chr11:62520584C>Tc.703G>Ac.(703-705)Gat>Aatp.D235N
BRCA116252083062520830+Missense_MutationSNPCCTTCGA-A8-A06Q-01A-11W-A050-09TCGA-A8-A06Q-10A-01W-A055-09g.chr11:62520830C>Tc.457G>Ac.(457-459)Gcc>Accp.A153T
BRCA116252083362520833+Missense_MutationSNPCCGTCGA-C8-A1HJ-01A-11D-A13L-09TCGA-C8-A1HJ-10A-01D-A13O-09g.chr11:62520833C>Gc.454G>Cc.(454-456)Gct>Cctp.A152P
BRCA116252091762520917+Missense_MutationSNPGGTTCGA-C8-A275-01A-21D-A16D-09TCGA-C8-A275-10A-01D-A16D-09g.chr11:62520917G>Tc.370C>Ac.(370-372)Cca>Acap.P124T
BRCA116252152062521520+Missense_MutationSNPGGTTCGA-AN-A046-01A-21W-A050-09TCGA-AN-A046-10A-01W-A055-09g.chr11:62521520G>Tc.15C>Ac.(13-15)ttC>ttAp.F5L
CESC116251984462519844+SilentSNPGGATCGA-EK-A2GZ-01A-11D-A17W-09TCGA-EK-A2GZ-10A-01D-A17W-09g.chr11:62519844G>Ac.1443C>Tc.(1441-1443)ttC>ttTp.F481F
CESC116252058662520586+Missense_MutationSNPGGATCGA-MY-A5BD-01A-11D-A26G-09TCGA-MY-A5BD-10A-01D-A26G-09g.chr11:62520586G>Ac.701C>Tc.(700-702)cCa>cTap.P234L
COAD116251959462519594+Missense_MutationSNPCCATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr11:62519594C>Ac.1693G>Tc.(1693-1695)Gat>Tatp.D565Y
COAD116252001662520016+Missense_MutationSNPTTCTCGA-D5-5541-01A-01D-1650-10TCGA-D5-5541-10A-02D-1650-10g.chr11:62520016T>Cc.1271A>Gc.(1270-1272)cAt>cGtp.H424R
COAD116252029462520294+SilentSNPGGATCGA-F4-6570-01A-11D-1771-10TCGA-F4-6570-10A-01D-1771-10g.chr11:62520294G>Ac.993C>Tc.(991-993)gcC>gcTp.A331A
COAD116252075862520758+Missense_MutationSNPCCTTCGA-AA-3672-01A-01W-0900-09TCGA-AA-3672-10A-01W-0900-09g.chr11:62520758C>Tc.529G>Ac.(529-531)Gca>Acap.A177T
COAD116252145962521461+In_Frame_DelDELGAAGAA-TCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr11:62521459_62521461delGAAc.74_76delTTCc.(73-78)cttcgt>cgtp.L25del
COADREAD116251959462519594+Missense_MutationSNPCCATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr11:62519594C>Ac.1693G>Tc.(1693-1695)Gat>Tatp.D565Y
COADREAD116252001662520016+Missense_MutationSNPTTCTCGA-D5-5541-01A-01D-1650-10TCGA-D5-5541-10A-02D-1650-10g.chr11:62520016T>Cc.1271A>Gc.(1270-1272)cAt>cGtp.H424R
COADREAD116252029462520294+SilentSNPGGATCGA-F4-6570-01A-11D-1771-10TCGA-F4-6570-10A-01D-1771-10g.chr11:62520294G>Ac.993C>Tc.(991-993)gcC>gcTp.A331A
COADREAD116252075862520758+Missense_MutationSNPCCTTCGA-AA-3672-01A-01W-0900-09TCGA-AA-3672-10A-01W-0900-09g.chr11:62520758C>Tc.529G>Ac.(529-531)Gca>Acap.A177T
COADREAD116252145962521461+In_Frame_DelDELGAAGAA-TCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr11:62521459_62521461delGAAc.74_76delTTCc.(73-78)cttcgt>cgtp.L25del
DLBC116251980662519806+Missense_MutationSNPTTCTCGA-G8-6325-01A-11D-2210-10TCGA-G8-6325-10A-01D-2210-10g.chr11:62519806T>Cc.1481A>Gc.(1480-1482)cAc>cGcp.H494R
ESCA116252114162521141+Missense_MutationSNPCCTTCGA-L5-A4OI-01A-11D-A27G-09TCGA-L5-A4OI-11A-11D-A27G-09g.chr11:62521141C>Tc.146G>Ac.(145-147)gGt>gAtp.G49D
GBMLGG116251964762519647+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62519647G>Tc.1640C>Ac.(1639-1641)cCt>cAtp.P547H
GBMLGG116251991662519916+SilentSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62519916G>Ac.1371C>Tc.(1369-1371)taC>taTp.Y457Y
GBMLGG116252027762520277+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62520277G>Ac.1010C>Tc.(1009-1011)gCt>gTtp.A337V
HNSC116252023462520234+SilentSNPCCGTCGA-BA-4075-01A-01D-1434-08TCGA-BA-4075-10A-01D-1434-08g.chr11:62520234C>Gc.1053G>Cc.(1051-1053)ctG>ctCp.L351L
HNSC116252030462520304+Missense_MutationSNPGGATCGA-D6-6516-01A-11D-1870-08TCGA-D6-6516-10A-01D-1870-08g.chr11:62520304G>Ac.983C>Tc.(982-984)cCa>cTap.P328L
HNSC116252030562520305+Missense_MutationSNPGGATCGA-D6-6516-01A-11D-1870-08TCGA-D6-6516-10A-01D-1870-08g.chr11:62520305G>Ac.982C>Tc.(982-984)Cca>Tcap.P328S
HNSC116252075562520755+Missense_MutationSNPCCTTCGA-QK-A6II-01A-11D-A31L-08TCGA-QK-A6II-10A-01D-A31J-08g.chr11:62520755C>Tc.532G>Ac.(532-534)Gac>Aacp.D178N
HNSC116252086762520867+SilentSNPCCGTCGA-P3-A6T6-01A-11D-A34J-08TCGA-P3-A6T6-10A-01D-A34M-08g.chr11:62520867C>Gc.420G>Cc.(418-420)ctG>ctCp.L140L
HNSC116252095162520951+Missense_MutationSNPAATTCGA-CQ-5331-01A-02D-1870-08TCGA-CQ-5331-10A-01D-1870-08g.chr11:62520951A>Tc.336T>Ac.(334-336)gaT>gaAp.D112E
HNSC116252103462521034+Missense_MutationSNPAAGTCGA-QK-A6II-01A-11D-A31L-08TCGA-QK-A6II-10A-01D-A31J-08g.chr11:62521034A>Gc.253T>Cc.(253-255)Ttc>Ctcp.F85L
HNSC116252107862521078+Missense_MutationSNPTTATCGA-CR-7389-01A-11D-2012-08TCGA-CR-7389-10A-01D-2013-08g.chr11:62521078T>Ac.209A>Tc.(208-210)cAg>cTgp.Q70L
HNSC116252147062521470+Missense_MutationSNPCCGTCGA-CV-A6JE-01A-11D-A31L-08TCGA-CV-A6JE-10A-01D-A31J-08g.chr11:62521470C>Gc.65G>Cc.(64-66)aGa>aCap.R22T
KIPAN116252028362520283+Missense_MutationSNPAATTCGA-P4-AAVL-01A-11D-A42J-10TCGA-P4-AAVL-11A-11D-A42M-10g.chr11:62520283A>Tc.1004T>Ac.(1003-1005)gTc>gAcp.V335D
KIRP116252028362520283+Missense_MutationSNPAATTCGA-P4-AAVL-01A-11D-A42J-10TCGA-P4-AAVL-11A-11D-A42M-10g.chr11:62520283A>Tc.1004T>Ac.(1003-1005)gTc>gAcp.V335D
LGG116251964762519647+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62519647G>Tc.1640C>Ac.(1639-1641)cCt>cAtp.P547H
LGG116251991662519916+SilentSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62519916G>Ac.1371C>Tc.(1369-1371)taC>taTp.Y457Y
LGG116252027762520277+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr11:62520277G>Ac.1010C>Tc.(1009-1011)gCt>gTtp.A337V
LIHC116252065362520653+Missense_MutationSNPTTCTCGA-ES-A2HS-01A-11D-A183-10TCGA-ES-A2HS-11A-11D-A183-10g.chr11:62520653T>Cc.634A>Gc.(634-636)Aca>Gcap.T212A
LIHC116252095362520953+Frame_Shift_DelDELCC-TCGA-G3-A3CJ-01A-11D-A20W-10TCGA-G3-A3CJ-10A-01D-A20W-10g.chr11:62520953delCc.334delGc.(334-336)gatfsp.D112fs
LIHC116252147162521471+Missense_MutationSNPTTCTCGA-DD-A39Z-01A-11D-A20W-10TCGA-DD-A39Z-11A-21D-A20W-10g.chr11:62521471T>Cc.64A>Gc.(64-66)Aga>Ggap.R22G
LUAD116251974562519745+SilentSNPGGATCGA-67-3771-01A-01D-1040-01TCGA-67-3771-10A-01D-1040-01g.chr11:62519745G>Ac.1542C>Tc.(1540-1542)gaC>gaTp.D514D
LUAD116251980562519805+Missense_MutationSNPGGCTCGA-MP-A4TE-01A-22D-A25L-08TCGA-MP-A4TE-10A-01D-A25L-08g.chr11:62519805G>Cc.1482C>Gc.(1480-1482)caC>caGp.H494Q
LUAD116251981362519813+Missense_MutationSNPTTCTCGA-05-4424-01A-22D-1855-08TCGA-05-4424-10A-01D-1855-08g.chr11:62519813T>Cc.1474A>Gc.(1474-1476)Acg>Gcgp.T492A
LUAD116251981462519814+SilentSNPGGATCGA-75-6205-01A-11D-1753-08TCGA-75-6205-10A-01D-1753-08g.chr11:62519814G>Ac.1473C>Tc.(1471-1473)gcC>gcTp.A491A
LUAD116251982562519825+SilentSNPGGTTCGA-17-Z015-01A-01W-0746-08TCGA-17-Z015-11A-01W-0746-08g.chr11:62519825G>Tc.1462C>Ac.(1462-1464)Cgg>Aggp.R488R
LUAD116251994762519947+Missense_MutationSNPAATTCGA-91-6828-01A-11D-1855-08TCGA-91-6828-10A-01D-1855-08g.chr11:62519947A>Tc.1340T>Ac.(1339-1341)cTg>cAgp.L447Q
LUAD116252014262520142+Missense_MutationSNPGGATCGA-44-7661-01A-11D-2063-08TCGA-44-7661-10A-01D-2063-08g.chr11:62520142G>Ac.1145C>Tc.(1144-1146)tCt>tTtp.S382F
LUAD116252080462520804+SilentSNPGGATCGA-44-7661-01A-11D-2063-08TCGA-44-7661-10A-01D-2063-08g.chr11:62520804G>Ac.483C>Tc.(481-483)atC>atTp.I161I
LUAD116252102262521022+Missense_MutationSNPGGATCGA-86-8278-01A-11D-2284-08TCGA-86-8278-10A-01D-2284-08g.chr11:62521022G>Ac.265C>Tc.(265-267)Cgg>Tggp.R89W
LUAD116252102262521022+Missense_MutationSNPGGCTCGA-55-7283-01A-11D-2036-08TCGA-55-7283-10A-01D-2036-08g.chr11:62521022G>Cc.265C>Gc.(265-267)Cgg>Gggp.R89G
LUSC116251963062519630+Missense_MutationSNPCCGTCGA-66-2785-01A-01D-1522-08TCGA-66-2785-11A-01D-1522-08g.chr11:62519630C>Gc.1657G>Cc.(1657-1659)Gac>Cacp.D553H
LUSC116252052862520528+SilentSNPGGATCGA-18-3411-01A-01D-0983-08TCGA-18-3411-11A-01D-0983-08g.chr11:62520528G>Ac.759C>Tc.(757-759)gaC>gaTp.D253D
LUSC116252102262521022+Missense_MutationSNPGGCTCGA-66-2766-01A-01D-1522-08TCGA-66-2766-11A-01D-1522-08g.chr11:62521022G>Cc.265C>Gc.(265-267)Cgg>Gggp.R89G
OV116251992862519928+SilentSNPCCTTCGA-23-1809-01A-01W-0633-09TCGA-23-1809-10A-01W-0634-09g.chr11:62519928C>Tc.1359G>Ac.(1357-1359)ctG>ctAp.L453L
OV116252002262520022+Missense_MutationSNPGGTTCGA-61-1722-01A-01D-1556-09TCGA-61-1722-11A-01W-0639-09g.chr11:62520022G>Tc.1265C>Ac.(1264-1266)cCc>cAcp.P422H
PRAD116251976862519768+Missense_MutationSNPGGATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr11:62519768G>Ac.1519C>Tc.(1519-1521)Cgg>Tggp.R507W
PRAD116251984462519844+Missense_MutationSNPGGCTCGA-EJ-5517-01A-01D-1576-08TCGA-EJ-5517-10A-01D-1577-08g.chr11:62519844G>Cc.1443C>Gc.(1441-1443)ttC>ttGp.F481L
SARC116252011062520110+Nonsense_MutationSNPGGATCGA-JV-A5VE-01A-11D-A29N-09TCGA-JV-A5VE-10A-01D-A29N-09g.chr11:62520110G>Ac.1177C>Tc.(1177-1179)Cag>Tagp.Q393*
SKCM116252011762520117+SilentSNPCCTTCGA-EE-A2GL-06A-11D-A196-08TCGA-EE-A2GL-10A-01D-A198-08g.chr11:62520117C>Tc.1170G>Ac.(1168-1170)caG>caAp.Q390Q
SKCM116252025662520256+Missense_MutationSNPGGATCGA-EE-A29V-06A-12D-A197-08TCGA-EE-A29V-10A-01D-A199-08g.chr11:62520256G>Ac.1031C>Tc.(1030-1032)cCa>cTap.P344L
SKCM116252025762520257+Missense_MutationSNPGGATCGA-EE-A29V-06A-12D-A197-08TCGA-EE-A29V-10A-01D-A199-08g.chr11:62520257G>Ac.1030C>Tc.(1030-1032)Cca>Tcap.P344S
SKCM116252074162520741+SilentSNPCCTTCGA-GN-A266-06A-11D-A197-08TCGA-GN-A266-10A-01D-A199-08g.chr11:62520741C>Tc.546G>Ac.(544-546)aaG>aaAp.K182K
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN116251995562519955single base substitutionGAdownstream_gene_variant
BLCA-CN116251995562519955single base substitutionGAsynonymous_variantP444P1332C>T
BLCA-CN116251995562519955single base substitutionGAupstream_gene_variant
BLCA-US116251990962519909single base substitutionCAdownstream_gene_variant
BLCA-US116251990962519909single base substitutionCAmissense_variantA460S1378G>T
BLCA-US116251990962519909single base substitutionCAupstream_gene_variant
BLCA-US116252102262521022single base substitutionGCmissense_variantR39G115C>G
BLCA-US116252102262521022single base substitutionGCmissense_variantR89G265C>G
BLCA-US116252102262521022single base substitutionGCupstream_gene_variant
BLCA-US116252149762521497single base substitutionGAintron_variant
BLCA-US116252149762521497single base substitutionGAmissense_variantS13L38C>T
BLCA-US116252149762521497single base substitutionGAupstream_gene_variant
BRCA-EU116251188762511887single base substitutionGAdownstream_gene_variant
BRCA-EU116251338762513387single base substitutionTGdownstream_gene_variant
BRCA-EU116251506862515068single base substitutionCTdownstream_gene_variant
BRCA-EU116251651062516510single base substitutionCGdownstream_gene_variant
BRCA-EU116251651062516510single base substitutionCGintron_variant
BRCA-EU116251670862516708single base substitutionCAdownstream_gene_variant
BRCA-EU116251670862516708single base substitutionCAintron_variant
BRCA-EU116251984462519844single base substitutionGCdownstream_gene_variant
BRCA-EU116251984462519844single base substitutionGCmissense_variantF481L1443C>G
BRCA-EU116251984462519844single base substitutionGCupstream_gene_variant
BRCA-EU116252003262520039deletion of <=200bpGGTCTGTT-downstream_gene_variant
BRCA-EU116252003262520039deletion of <=200bpGGTCTGTT-frameshift_variantPTDP416
BRCA-EU116252003262520039deletion of <=200bpGGTCTGTT-upstream_gene_variant
BRCA-EU116252005562520055single base substitutionCGdownstream_gene_variant
BRCA-EU116252005562520055single base substitutionCGmissense_variantS411T1232G>C
BRCA-EU116252005562520055single base substitutionCGupstream_gene_variant
BRCA-EU116252112662521126single base substitutionGCmissense_variantP4R11C>G
BRCA-EU116252112662521126single base substitutionGCmissense_variantP54R161C>G
BRCA-EU116252112662521126single base substitutionGCupstream_gene_variant
BRCA-EU116252139062521390single base substitutionCAintron_variant
BRCA-EU116252139062521390single base substitutionCAupstream_gene_variant
BRCA-EU116252145962521459single base substitutionGCintron_variant
BRCA-EU116252145962521459single base substitutionGCmissense_variantR26G76C>G
BRCA-EU116252145962521459single base substitutionGCupstream_gene_variant
BRCA-EU116252176462521764single base substitutionATupstream_gene_variant
BRCA-EU116252193562521935single base substitutionGTupstream_gene_variant
BRCA-EU116252286562522865single base substitutionCGupstream_gene_variant
BRCA-EU116252435662524356single base substitutionATupstream_gene_variant
BRCA-EU116252436562524365single base substitutionTAupstream_gene_variant
BRCA-EU116252488562524885single base substitutionCTupstream_gene_variant
BRCA-EU116252573362525733single base substitutionTAupstream_gene_variant
BRCA-EU116252576162525761single base substitutionGCupstream_gene_variant
BRCA-EU116252591062525910single base substitutionAGupstream_gene_variant
BRCA-EU116252647762526477single base substitutionCGupstream_gene_variant
BRCA-FR116251651062516510single base substitutionCGdownstream_gene_variant
BRCA-FR116251651062516510single base substitutionCGintron_variant
BRCA-FR116251984462519844single base substitutionGCdownstream_gene_variant
BRCA-FR116251984462519844single base substitutionGCmissense_variantF481L1443C>G
BRCA-FR116251984462519844single base substitutionGCupstream_gene_variant
BRCA-FR116252145962521459single base substitutionGCintron_variant
BRCA-FR116252145962521459single base substitutionGCmissense_variantR26G76C>G
BRCA-FR116252145962521459single base substitutionGCupstream_gene_variant
BRCA-FR116252286562522865single base substitutionCGupstream_gene_variant
BRCA-UK116252502662525026single base substitutionTCupstream_gene_variant
BRCA-UK116252591062525910single base substitutionAGupstream_gene_variant
BRCA-US116252058462520584single base substitutionCTdownstream_gene_variant
BRCA-US116252058462520584single base substitutionCTmissense_variantD235N703G>A
BRCA-US116252058462520584single base substitutionCTupstream_gene_variant
BRCA-US116252083062520830single base substitutionCTmissense_variantA103T307G>A
BRCA-US116252083062520830single base substitutionCTmissense_variantA153T457G>A
BRCA-US116252083062520830single base substitutionCTupstream_gene_variant
BRCA-US116252083362520833single base substitutionCGmissense_variantA102P304G>C
BRCA-US116252083362520833single base substitutionCGmissense_variantA152P454G>C
BRCA-US116252083362520833single base substitutionCGupstream_gene_variant
BRCA-US116252091762520917single base substitutionGTmissense_variantP124T370C>A
BRCA-US116252091762520917single base substitutionGTmissense_variantP74T220C>A
BRCA-US116252091762520917single base substitutionGTupstream_gene_variant
BRCA-US116252152062521520single base substitutionGTintron_variant
BRCA-US116252152062521520single base substitutionGTmissense_variantF5L15C>A
BRCA-US116252152062521520single base substitutionGTupstream_gene_variant
BTCA-JP116252143562521435single base substitutionCAintron_variant
BTCA-JP116252143562521435single base substitutionCAsplice_donor_variant
BTCA-JP116252143562521435single base substitutionCAupstream_gene_variant
BTCA-JP116252149762521497single base substitutionGAintron_variant
BTCA-JP116252149762521497single base substitutionGAmissense_variantS13L38C>T
BTCA-JP116252149762521497single base substitutionGAupstream_gene_variant
CESC-US116251984462519844single base substitutionGAdownstream_gene_variant
CESC-US116251984462519844single base substitutionGAsynonymous_variantF481F1443C>T
CESC-US116251984462519844single base substitutionGAupstream_gene_variant
CESC-US116252058662520586single base substitutionGAdownstream_gene_variant
CESC-US116252058662520586single base substitutionGAmissense_variantP234L701C>T
CESC-US116252058662520586single base substitutionGAupstream_gene_variant
CLLE-ES116251225662512256single base substitutionCTdownstream_gene_variant
COAD-US116252029462520294single base substitutionGAdownstream_gene_variant
COAD-US116252029462520294single base substitutionGAsynonymous_variantA331A993C>T
COAD-US116252029462520294single base substitutionGAupstream_gene_variant
COAD-US116252145962521461deletion of <=200bpGAA-disruptive_inframe_deletionLR25R
COAD-US116252145962521461deletion of <=200bpGAA-intron_variant
COAD-US116252145962521461deletion of <=200bpGAA-upstream_gene_variant
COAD-US116252147562521475single base substitutionTCintron_variant
COAD-US116252147562521475single base substitutionTCsynonymous_variantR20R60A>G
COAD-US116252147562521475single base substitutionTCupstream_gene_variant
COCA-CN116251403962514039single base substitutionGAdownstream_gene_variant
COCA-CN116251555462515554single base substitutionTGdownstream_gene_variant
COCA-CN116251746462517464single base substitutionTCdownstream_gene_variant
COCA-CN116251746462517464single base substitutionTCintron_variant
COCA-CN116252010862520108single base substitutionCTdownstream_gene_variant
COCA-CN116252010862520108single base substitutionCTsynonymous_variantQ393Q1179G>A
COCA-CN116252010862520108single base substitutionCTupstream_gene_variant
COCA-CN116252458262524582single base substitutionATupstream_gene_variant
ESAD-UK116251093962510939single base substitutionGAdownstream_gene_variant
ESAD-UK116251169662511696single base substitutionGCdownstream_gene_variant
ESAD-UK116251669462516694single base substitutionCTdownstream_gene_variant
ESAD-UK116251669462516694single base substitutionCTintron_variant
ESAD-UK116251680862516808single base substitutionTCdownstream_gene_variant
ESAD-UK116251680862516808single base substitutionTCintron_variant
ESAD-UK116252309562523095single base substitutionCAupstream_gene_variant
ESAD-UK116252388362523883single base substitutionAGupstream_gene_variant
ESAD-UK116252390762523907single base substitutionCAupstream_gene_variant
ESAD-UK116252486562524865single base substitutionGCupstream_gene_variant
ESCA-CN116252143162521431single base substitutionCAintron_variant
ESCA-CN116252143162521431single base substitutionCAupstream_gene_variant
KIRC-US116252059062520590single base substitutionGAdownstream_gene_variant
KIRC-US116252059062520590single base substitutionGAmissense_variantP233S697C>T
KIRC-US116252059062520590single base substitutionGAupstream_gene_variant
KIRP-US116251973962519739single base substitutionGAdownstream_gene_variant
KIRP-US116251973962519739single base substitutionGAsynonymous_variantY516Y1548C>T
KIRP-US116251973962519739single base substitutionGAupstream_gene_variant
LAML-KR116251371262513712single base substitutionGTdownstream_gene_variant
LAML-KR116251420362514203single base substitutionCTdownstream_gene_variant
LAML-KR116251420462514204single base substitutionAGdownstream_gene_variant
LICA-FR116251956462519564single base substitutionATdownstream_gene_variant
LICA-FR116251956462519564single base substitutionATexon_variant
LICA-FR116251956462519564single base substitutionATstop_lost*575K1723T>A
LICA-FR116252420262524202single base substitutionCAupstream_gene_variant
LINC-JP116252086462520864single base substitutionTCsynonymous_variantR141R423A>G
LINC-JP116252086462520864single base substitutionTCsynonymous_variantR91R273A>G
LINC-JP116252086462520864single base substitutionTCupstream_gene_variant
LINC-JP116252118162521181single base substitutionTC5_prime_UTR_variant
LINC-JP116252118162521181single base substitutionTCmissense_variantT36A106A>G
LINC-JP116252118162521181single base substitutionTCupstream_gene_variant
LINC-JP116252459462524594single base substitutionGAupstream_gene_variant
LIRI-JP116251542762515427single base substitutionCAdownstream_gene_variant
LIRI-JP116251906762519067single base substitutionCA3_prime_UTR_variant
LIRI-JP116251906762519067single base substitutionCAdownstream_gene_variant
LIRI-JP116251906762519067single base substitutionCAintron_variant
LIRI-JP116251920262519202single base substitutionCT3_prime_UTR_variant
LIRI-JP116251920262519202single base substitutionCTdownstream_gene_variant
LIRI-JP116251920262519202single base substitutionCTintron_variant
LIRI-JP116251982962519829single base substitutionTCdownstream_gene_variant
LIRI-JP116251982962519829single base substitutionTCsynonymous_variantT486T1458A>G
LIRI-JP116251982962519829single base substitutionTCupstream_gene_variant
LIRI-JP116252158062521580single base substitutionAG5_prime_UTR_variant
LIRI-JP116252158062521580single base substitutionAGintron_variant
LIRI-JP116252158062521580single base substitutionAGupstream_gene_variant
LIRI-JP116252189762521897single base substitutionCAupstream_gene_variant
LIRI-JP116252250662522506single base substitutionCTupstream_gene_variant
LIRI-JP116252381962523819single base substitutionGAupstream_gene_variant
LUSC-KR116252355962523559single base substitutionGAupstream_gene_variant
LUSC-KR116252517662525176single base substitutionTCupstream_gene_variant
LUSC-US116251963062519630single base substitutionCGdownstream_gene_variant
LUSC-US116251963062519630single base substitutionCGmissense_variantD553H1657G>C
LUSC-US116251963062519630single base substitutionCGupstream_gene_variant
LUSC-US116252052862520528single base substitutionGAdownstream_gene_variant
LUSC-US116252052862520528single base substitutionGAsynonymous_variantD253D759C>T
LUSC-US116252052862520528single base substitutionGAupstream_gene_variant
LUSC-US116252102262521022single base substitutionGCmissense_variantR39G115C>G
LUSC-US116252102262521022single base substitutionGCmissense_variantR89G265C>G
LUSC-US116252102262521022single base substitutionGCupstream_gene_variant
MALY-DE116251527662515276single base substitutionATdownstream_gene_variant
MALY-DE116251717262517209deletion of <=200bpCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCT-downstream_gene_variant
MALY-DE116251717262517209deletion of <=200bpCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCT-intron_variant
MALY-DE116251989862519898single base substitutionGAdownstream_gene_variant
MALY-DE116251989862519898single base substitutionGAsynonymous_variantS463S1389C>T
MALY-DE116251989862519898single base substitutionGAupstream_gene_variant
MALY-DE116252167862521678single base substitutionCGupstream_gene_variant
MALY-DE116252270962522709single base substitutionACupstream_gene_variant
MALY-DE116252459962524599single base substitutionTGupstream_gene_variant
MELA-AU116251092562510925single base substitutionGAdownstream_gene_variant
MELA-AU116251112262511122single base substitutionTCdownstream_gene_variant
MELA-AU116251204162512041single base substitutionCTdownstream_gene_variant
MELA-AU116251212262512122single base substitutionCTdownstream_gene_variant
MELA-AU116251337062513370single base substitutionCTdownstream_gene_variant
MELA-AU116251385562513855single base substitutionGAdownstream_gene_variant
MELA-AU116251404962514050multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU116251405062514050single base substitutionCTdownstream_gene_variant
MELA-AU116251441262514412single base substitutionCAdownstream_gene_variant
MELA-AU116251528262515282single base substitutionAGdownstream_gene_variant
MELA-AU116251771262517712single base substitutionGAdownstream_gene_variant
MELA-AU116251771262517712single base substitutionGAintron_variant
MELA-AU116251830762518307single base substitutionCTdownstream_gene_variant
MELA-AU116251830762518307single base substitutionCTintron_variant
MELA-AU116251888162518881single base substitutionCT3_prime_UTR_variant
MELA-AU116251888162518881single base substitutionCTdownstream_gene_variant
MELA-AU116251888162518881single base substitutionCTintron_variant
MELA-AU116251922362519223single base substitutionGA3_prime_UTR_variant
MELA-AU116251922362519223single base substitutionGAdownstream_gene_variant
MELA-AU116251922362519223single base substitutionGAintron_variant
MELA-AU116251997162519971single base substitutionGTdownstream_gene_variant
MELA-AU116251997162519971single base substitutionGTstop_gainedS439*1316C>A
MELA-AU116251997162519971single base substitutionGTupstream_gene_variant
MELA-AU116252005562520055single base substitutionCTdownstream_gene_variant
MELA-AU116252005562520055single base substitutionCTmissense_variantS411N1232G>A
MELA-AU116252005562520055single base substitutionCTupstream_gene_variant
MELA-AU116252034262520342single base substitutionTCdownstream_gene_variant
MELA-AU116252034262520342single base substitutionTCsynonymous_variantG315G945A>G
MELA-AU116252034262520342single base substitutionTCupstream_gene_variant
MELA-AU116252085462520854single base substitutionGAmissense_variantP145S433C>T
MELA-AU116252085462520854single base substitutionGAmissense_variantP95S283C>T
MELA-AU116252085462520854single base substitutionGAupstream_gene_variant
MELA-AU116252135562521355single base substitutionGAintron_variant
MELA-AU116252135562521355single base substitutionGAupstream_gene_variant
MELA-AU116252137662521376single base substitutionGAintron_variant
MELA-AU116252137662521376single base substitutionGAupstream_gene_variant
MELA-AU116252139362521393single base substitutionGAintron_variant
MELA-AU116252139362521393single base substitutionGAupstream_gene_variant
MELA-AU116252141862521418single base substitutionCTintron_variant
MELA-AU116252141862521418single base substitutionCTupstream_gene_variant
MELA-AU116252163762521637single base substitutionCT5_prime_UTR_variant
MELA-AU116252163762521637single base substitutionCTupstream_gene_variant
MELA-AU116252170262521703multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU116252194862521948single base substitutionGAupstream_gene_variant
MELA-AU116252238962522389single base substitutionCTupstream_gene_variant
MELA-AU116252273762522737single base substitutionCTupstream_gene_variant
MELA-AU116252318162523181single base substitutionCTupstream_gene_variant
MELA-AU116252422362524223single base substitutionCTupstream_gene_variant
MELA-AU116252449862524498single base substitutionCTupstream_gene_variant
MELA-AU116252450262524502single base substitutionCTupstream_gene_variant
MELA-AU116252497062524970single base substitutionTCupstream_gene_variant
MELA-AU116252499862524998single base substitutionCTupstream_gene_variant
MELA-AU116252503062525030single base substitutionTCupstream_gene_variant
MELA-AU116252537662525376single base substitutionGAupstream_gene_variant
MELA-AU116252548362525483single base substitutionCTupstream_gene_variant
MELA-AU116252571462525714single base substitutionCTupstream_gene_variant
MELA-AU116252628962526289single base substitutionGAupstream_gene_variant
MELA-AU116252638562526385single base substitutionCTupstream_gene_variant
MELA-AU116252639362526393single base substitutionCTupstream_gene_variant
MELA-AU116252652462526525multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
ORCA-IN116252019462520194single base substitutionCGdownstream_gene_variant
ORCA-IN116252019462520194single base substitutionCGmissense_variantE365Q1093G>C
ORCA-IN116252019462520194single base substitutionCGupstream_gene_variant
OV-AU116251311162513111single base substitutionGCdownstream_gene_variant
OV-AU116251609162516091single base substitutionAG3_prime_UTR_variant
OV-AU116251609162516091single base substitutionAGdownstream_gene_variant
PACA-AU116251182062511820single base substitutionCTdownstream_gene_variant
PACA-AU116251527962515279single base substitutionTGdownstream_gene_variant
PACA-AU116252516062525160single base substitutionCTupstream_gene_variant
PACA-CA116251143362511433single base substitutionCGdownstream_gene_variant
PACA-CA116251235462512354single base substitutionAGdownstream_gene_variant
PACA-CA116251392262513922single base substitutionGCdownstream_gene_variant
PACA-CA116251527662515276single base substitutionATdownstream_gene_variant
PACA-CA116251528062515280single base substitutionTAdownstream_gene_variant
PACA-CA116252298462522984single base substitutionTGupstream_gene_variant
PRAD-UK116251525862515258single base substitutionGAdownstream_gene_variant
PRAD-UK116252501062525010single base substitutionCTupstream_gene_variant
PRAD-US116251984462519844single base substitutionGCdownstream_gene_variant
PRAD-US116251984462519844single base substitutionGCmissense_variantF481L1443C>G
PRAD-US116251984462519844single base substitutionGCupstream_gene_variant
READ-US116252051562520515single base substitutionGAdownstream_gene_variant
READ-US116252051562520515single base substitutionGAmissense_variantR258W772C>T
READ-US116252051562520515single base substitutionGAupstream_gene_variant
RECA-EU116251853262518532single base substitutionGA3_prime_UTR_variant
RECA-EU116251853262518532single base substitutionGAdownstream_gene_variant
RECA-EU116251853262518532single base substitutionGAintron_variant
RECA-EU116252165062521650single base substitutionCT5_prime_UTR_variant
RECA-EU116252165062521650single base substitutionCTupstream_gene_variant
SKCA-BR116251260762512607single base substitutionGAdownstream_gene_variant
SKCA-BR116251400762514008deletion of <=200bpTG-downstream_gene_variant
SKCA-BR116251412962514129single base substitutionGAdownstream_gene_variant
SKCA-BR116251647462516474single base substitutionGTdownstream_gene_variant
SKCA-BR116251647462516474single base substitutionGTintron_variant
SKCA-BR116251723962517239single base substitutionACdownstream_gene_variant
SKCA-BR116251723962517239single base substitutionACintron_variant
SKCA-BR116251885062518850single base substitutionTG3_prime_UTR_variant
SKCA-BR116251885062518850single base substitutionTGdownstream_gene_variant
SKCA-BR116251885062518850single base substitutionTGintron_variant
SKCA-BR116252454662524546single base substitutionATupstream_gene_variant
SKCA-BR116252458262524582single base substitutionATupstream_gene_variant
SKCA-BR116252516762525167single base substitutionTCupstream_gene_variant
SKCM-US116252011762520117single base substitutionCTdownstream_gene_variant
SKCM-US116252011762520117single base substitutionCTsynonymous_variantQ390Q1170G>A
SKCM-US116252011762520117single base substitutionCTupstream_gene_variant
SKCM-US116252074162520741single base substitutionCTdownstream_gene_variant
SKCM-US116252074162520741single base substitutionCTsynonymous_variantK182K546G>A
SKCM-US116252074162520741single base substitutionCTupstream_gene_variant
SKCM-US116252107162521071single base substitutionGAsynonymous_variantF22F66C>T
SKCM-US116252107162521071single base substitutionGAsynonymous_variantF72F216C>T
SKCM-US116252107162521071single base substitutionGAupstream_gene_variant
STAD-US116251982162519821single base substitutionCTdownstream_gene_variant
STAD-US116251982162519821single base substitutionCTmissense_variantR489Q1466G>A
STAD-US116251982162519821single base substitutionCTupstream_gene_variant
STAD-US116251982562519825single base substitutionGAdownstream_gene_variant
STAD-US116251982562519825single base substitutionGAmissense_variantR488W1462C>T
STAD-US116251982562519825single base substitutionGAupstream_gene_variant
STAD-US116251984362519845deletion of <=200bpAGA-disruptive_inframe_deletionFS481S
STAD-US116251984362519845deletion of <=200bpAGA-downstream_gene_variant
STAD-US116251984362519845deletion of <=200bpAGA-upstream_gene_variant
STAD-US116251993962519939single base substitutionGAdownstream_gene_variant
STAD-US116251993962519939single base substitutionGAmissense_variantP450S1348C>T
STAD-US116251993962519939single base substitutionGAupstream_gene_variant
STAD-US116252019562520195single base substitutionTGdownstream_gene_variant
STAD-US116252019562520195single base substitutionTGmissense_variantE364D1092A>C
STAD-US116252019562520195single base substitutionTGupstream_gene_variant
STAD-US116252049862520498single base substitutionTAdownstream_gene_variant
STAD-US116252049862520498single base substitutionTAsynonymous_variantP263P789A>T
STAD-US116252049862520498single base substitutionTAupstream_gene_variant
THCA-US116252040162520401single base substitutionGAdownstream_gene_variant
THCA-US116252040162520401single base substitutionGAsynonymous_variantL296L886C>T
THCA-US116252040162520401single base substitutionGAupstream_gene_variant
UCEC-US116252048762520487single base substitutionATdownstream_gene_variant
UCEC-US116252048762520487single base substitutionATmissense_variantV267D800T>A
UCEC-US116252048762520487single base substitutionATupstream_gene_variant
UCEC-US116252061562520615single base substitutionACdownstream_gene_variant
UCEC-US116252061562520615single base substitutionACsynonymous_variantS224S672T>G
UCEC-US116252061562520615single base substitutionACupstream_gene_variant
UCEC-US116252078862520788single base substitutionGAdownstream_gene_variant
UCEC-US116252078862520788single base substitutionGAmissense_variantR167W499C>T
UCEC-US116252078862520788single base substitutionGAupstream_gene_variant
UCEC-US116252101362521013single base substitutionGAsynonymous_variantL42L124C>T
UCEC-US116252101362521013single base substitutionGAsynonymous_variantL92L274C>T
UCEC-US116252101362521013single base substitutionGAupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-EL-A3T3-01COSM2039607c.886C>Tp.L296LSubstitution - coding silent11:62752929-62752929-
TCGA-23-1809-01COSM1322291c.1359G>Ap.L453LSubstitution - coding silent11:62752456-62752456-
sysucc-880TCOSM5462060c.1179G>Ap.Q393QSubstitution - coding silent11:62752636-62752636-
TCGA-66-2785-01COSM689850c.1657G>Cp.D553HSubstitution - Missense11:62752158-62752158-
TCGA-18-3411-01COSM689849c.759C>Tp.D253DSubstitution - coding silent11:62753056-62753056-
SJHGG099_DCOSM4971796c.895C>Tp.L299FSubstitution - Missense11:62752920-62752920-
HCC1143COSM33515c.1271A>Tp.H424LSubstitution - Missense11:62752544-62752544-
TCGA-AM-5821-01COSM3752587c.60A>Gp.R20RSubstitution - coding silent11:62754003-62754003-
CHC320TCOSM251209c.1723T>Ap.*575KNonstop extension11:62752092-62752092-
TCGA-C8-A275-01COSM1475668c.370C>Ap.P124TSubstitution - Missense11:62753445-62753445-
BD114TCOSM5503749c.99+1G>Tp.?Unknown11:62753963-62753963-
ZZUFHECRKL-G035TCOSM5440324c.99+5G>Tp.?Unknown11:62753959-62753959-
67COSM5016361c.688_705del18p.T230_D235delTVRPPDDeletion - In frame11:62753110-62753127-
OSCC-GB_00070111COSM3710375c.1093G>Cp.E365QSubstitution - Missense11:62752722-62752722-
TCGA-EI-6882-01COSM3416073c.772C>Tp.R258WSubstitution - Missense11:62753043-62753043-
RK029_C01COSM1628140c.1458A>Gp.T486TSubstitution - coding silent11:62752357-62752357-
T3225COSM4742121c.986C>Tp.T329MSubstitution - Missense11:62752829-62752829-
TCGA-B8-4622-01COSM467153c.697C>Tp.P233SSubstitution - Missense11:62753118-62753118-
RK029_CCOSM1628140c.1458A>Gp.T486TSubstitution - coding silent11:62752357-62752357-
TCGA-BR-6452-01COSM4034888c.789A>Tp.P263PSubstitution - coding silent11:62753026-62753026-
TCGA-A8-A06Q-01COSM429469c.457G>Ap.A153TSubstitution - Missense11:62753358-62753358-
TCGA-24-0975-01COSM117917c.79G>Tp.G27*Substitution - Nonsense11:62753984-62753984-
HCT8COSM4199037c.975C>Tp.A325ASubstitution - coding silent11:62752840-62752840-
YUKATCOSM5373109c.1375G>Ap.A459TSubstitution - Missense11:62752440-62752440-
CSCC-55-TCOSM4528442c.1537G>Ap.G513RSubstitution - Missense11:62752278-62752278-
HCC26TCOSM3666482c.106A>Gp.T36ASubstitution - Missense11:62753709-62753709-
TCGA-BR-4370-01COSM4034886c.1348C>Tp.P450SSubstitution - Missense11:62752467-62752467-
HCT-15COSM1676117c.236T>Cp.M79TSubstitution - Missense11:62753579-62753579-
61COSM5739289c.685C>Tp.P229SSubstitution - Missense11:62753130-62753130-
SJHGG099_DCOSM4971795c.890C>Tp.P297LSubstitution - Missense11:62752925-62752925-
TCGA-GN-A266-06COSM3869767c.546G>Ap.K182KSubstitution - coding silent11:62753269-62753269-
B84COSM1746406c.1332C>Tp.P444PSubstitution - coding silent11:62752483-62752483-
TCGA-B5-A0JR-01COSM929810c.274C>Tp.L92LSubstitution - coding silent11:62753541-62753541-
RKOCOSM4647395c.142T>Cp.W48RSubstitution - Missense11:62753673-62753673-
TCGA-BR-A4QL-01COSM4034885c.1462C>Tp.R488WSubstitution - Missense11:62752353-62752353-
TCGA-BS-A0UL-01COSM929807c.800T>Ap.V267DSubstitution - Missense11:62753015-62753015-
CHC320TCOSM251209c.1723T>Ap.*575KNonstop extension11:62752092-62752092-
LUAD-F00162COSM366080c.1582G>Ap.A528TSubstitution - Missense11:62752233-62752233-
TCGA-B9-4115-01COSM3986308c.1548C>Tp.Y516YSubstitution - coding silent11:62752267-62752267-
TCGA-DK-A1AC-01COSM1298337c.1378G>Tp.A460SSubstitution - Missense11:62752437-62752437-
SJHGG099_DCOSM4971794c.839C>Tp.P280LSubstitution - Missense11:62752976-62752976-
TCGA-61-1722-01COSM1322290c.1265C>Ap.P422HSubstitution - Missense11:62752550-62752550-
BN37TCOSM1604920c.423A>Gp.R141RSubstitution - coding silent11:62753392-62753392-
TCGA-EE-A2GL-06COSM3451077c.1170G>Ap.Q390QSubstitution - coding silent11:62752645-62752645-
TCGA-CM-6171-01COSM1355459c.74_76delTTCp.L25delLDeletion - In frame11:62753987-62753989-
TCGA-EJ-5517-01COSM1127703c.1443C>Gp.F481LSubstitution - Missense11:62752372-62752372-
TCGA-66-2766-01COSM689848c.265C>Gp.R89GSubstitution - Missense11:62753550-62753550-
SJHGG099_DCOSM4971797c.785C>Tp.P262LSubstitution - Missense11:62753030-62753030-
PD13608aCOSM5767623c.76C>Gp.R26GSubstitution - Missense11:62753987-62753987-
TCGA-MY-A5BD-01COSM4855544c.701C>Tp.P234LSubstitution - Missense11:62753114-62753114-
PD7211aCOSM5775017c.161C>Gp.P54RSubstitution - Missense11:62753654-62753654-
2497773COSM5750410c.1372G>Tp.E458*Substitution - Nonsense11:62752443-62752443-
CMLPh-008COSM4424158c.1249A>Gp.T417ASubstitution - Missense11:62752566-62752566-
I2L-P19Ta-Tumor-OrganoidCOSM5367808c.100-6_100-5insTp.?Unknown11:62753720-62753721-
7TCOSM3710375c.1093G>Cp.E365QSubstitution - Missense11:62752722-62752722-
HCT15COSM1676117c.236T>Cp.M79TSubstitution - Missense11:62753579-62753579-
HCC2998COSM1676116c.400T>Cp.Y134HSubstitution - Missense11:62753415-62753415-
DLD1COSM4622226c.1564G>Ap.A522TSubstitution - Missense11:62752251-62752251-
TCGA-CD-A4MH-01COSM4034884c.1466G>Ap.R489QSubstitution - Missense11:62752349-62752349-
DLD1COSM1676117c.236T>Cp.M79TSubstitution - Missense11:62753579-62753579-
19COSM5747260c.362T>Gp.V121GSubstitution - Missense11:62753453-62753453-
TCGA-AA-3672-01COSM267786c.529G>Ap.A177TSubstitution - Missense11:62753286-62753286-
SA229COSM212656c.1388G>Cp.S463TSubstitution - Missense11:62752427-62752427-
TCGA-CG-5721-01COSM4034887c.1092A>Cp.E364DSubstitution - Missense11:62752723-62752723-
DN12171COSM5767623c.76C>Gp.R26GSubstitution - Missense11:62753987-62753987-
TCGA-B5-A11E-01COSM929808c.672T>Gp.S224SSubstitution - coding silent11:62753143-62753143-
B84-TumorCOSM1746406c.1332C>Tp.P444PSubstitution - coding silent11:62752483-62752483-
TCGA-F4-6570-01COSM1355458c.993C>Tp.A331ASubstitution - coding silent11:62752822-62752822-
I2L-P19Ta-Tumor-BiopsyCOSM5367808c.100-6_100-5insTp.?Unknown11:62753720-62753721-
LUAD-5V8LTCOSM401225c.515G>Tp.R172LSubstitution - Missense11:62753300-62753300-
TCGA-E2-A10B-01COSM429468c.703G>Ap.D235NSubstitution - Missense11:62753112-62753112-
ESCC_17COSM5625888c.20A>Gp.K7RSubstitution - Missense11:62754043-62754043-
104875COSM95555c.1493G>Ap.R498QSubstitution - Missense11:62752322-62752322-
MM1SCOSM1235541c.944G>Cp.G315ASubstitution - Missense11:62752871-62752871-
HCC1395COSM32758c.1364C>Tp.S455FSubstitution - Missense11:62752451-62752451-
TCGA-EB-A3XC-01COSM3451078c.216C>Tp.F72FSubstitution - coding silent11:62753599-62753599-
PR-09-5245COSM248409c.12G>Ap.E4ESubstitution - coding silent11:62754051-62754051-
T3503COSM4742120c.1002T>Cp.P334PSubstitution - coding silent11:62752813-62752813-
2492729COSM5726934c.501G>Ap.R167RSubstitution - coding silent11:62753314-62753314-
S00936COSM316641c.1401delTp.F467fs*75Deletion - Frameshift11:62752414-62752414-
PTC-7CCOSM4146021c.1622T>Gp.L541RSubstitution - Missense11:62752193-62752193-
H1155COSM1195796c.284G>Ap.C95YSubstitution - Missense11:62753531-62753531-
587342COSM1233136c.503G>Ap.R168QSubstitution - Missense11:62753312-62753312-
TCGA-06-0124COSM2149289c.1548delCp.R517fs*25Deletion - Frameshift11:62752267-62752267-
LS180COSM2039610c.771G>Ap.L257LSubstitution - coding silent11:62753044-62753044-
TCGA-BT-A20R-01COSM1298338c.38C>Tp.S13LSubstitution - Missense11:62754025-62754025-
TCGA-C8-A1HJ-01COSM1475667c.454G>Cp.A152PSubstitution - Missense11:62753361-62753361-
TCGA-AP-A0LP-01COSM929809c.499C>Tp.R167WSubstitution - Missense11:62753316-62753316-
TCGA-BT-A3PK-01COSM689848c.265C>Gp.R89GSubstitution - Missense11:62753550-62753550-
MOLT-4COSM1676115c.1465C>Tp.R489*Substitution - Nonsense11:62752350-62752350-
HCC26COSM3666482c.106A>Gp.T36ASubstitution - Missense11:62753709-62753709-
HCC2998COSM1676116c.400T>Cp.Y134HSubstitution - Missense11:62753415-62753415-
TCGA-EK-A2GZ-01COSM4831089c.1443C>Tp.F481FSubstitution - coding silent11:62752372-62752372-
46MCOSM5589388c.55G>Ap.E19KSubstitution - Missense11:62754008-62754008-
LS174TCOSM2039610c.771G>Ap.L257LSubstitution - coding silent11:62753044-62753044-
2492729COSM5726933c.609C>Tp.T203TSubstitution - coding silent11:62753206-62753206-
S02360COSM5695961c.763_789del27p.P255_P263delPHLRAPHPPDeletion - In frame11:62753026-62753052-
TCGA-AN-A046-01COSM3809864c.15C>Ap.F5LSubstitution - Missense11:62754048-62754048-
HCT8COSM1676117c.236T>Cp.M79TSubstitution - Missense11:62753579-62753579-
S02360COSM5695960c.793delGp.A265fs*42Deletion - Frameshift11:62753022-62753022-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.147526;Hs.147531;Hs.147533;Hs.147540;Hs.147545;Hs.147550;Hs.14755411q12.3887461|dbSNP|BC025249|A/G|non-coding||2495|Candidate;
887462|dbSNP|BC025249|A/G|non-coding||2516|Candidate
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
-A3-UTRInsertion.c.1722+142dupT1162519423CM
A-Frameshiftp.F467Lfs*75c.1401delT1162519886SCLC
ATMissensep.D112Ec.336T>A1162520951HNSC
ATMissensep.H424Lc.1271A>T1162520016BRCA
ATMissensep.L447Qc.1340T>A1162519947LUAD
ATMissensep.V267Dc.800T>A1162520487UCEC
CANonsensep.G27*c.79G>T1162521456OV
CGMissensep.A152Pc.454G>C1162520833BRCA
CGMissensep.S463Tc.1388G>C1162519899BRCA
CGSynonymousp.L140Lc.420G>C1162520867BRCA
CGSynonymousp.L351Lc.1053G>C1162520234HNSC
CT5-UTRSNV.c.1-102G>A1162521636CM
CTMissensep.A153Tc.457G>A1162520830BRCA
CTMissensep.D235Nc.703G>A1162520584BRCA
CTMissensep.S455Fc.1364C>T1162519923BRCA
CTSynonymousp.Q390Qc.1170G>A1162520117CM
GA5-UTRSNV.c.1-26C>T1162521560CM
GAMissensep.P233Sc.697C>T1162520590RCCC
GAMissensep.P450Sc.1348C>T1162519939STAD
GAMissensep.R167Wc.499C>T1162520788UCEC
GAMissensep.S13Lc.38C>T1162521497BLCA
GASynonymousp.A491Ac.1473C>T1162519814LUAD
GASynonymousp.D253Dc.759C>T1162520528LUSC
GASynonymousp.D514Dc.1542C>T1162519745LUAD
GASynonymousp.L296Lc.886C>T1162520401THCA
GASynonymousp.L92Lc.274C>T1162521013UCEC
GCMissensep.F481Lc.1443C>G1162519844PRAD
GCMissensep.R89Gc.265C>G1162521022BLCA
GCMissensep.R89Gc.265C>G1162521022LUSC
GGAAMissensep.P344Lc.1030_1031delinsTT1162520256CM
GTMissensep.P124Tc.370C>A1162520917BRCA
GTMissensep.S285Yc.854C>A1162520433LUAD
GTSynonymousp.R488Rc.1462C>A1162519825LUAD
TAGA-Frameshiftp.L515Pfs*26c.1544_1547delTCTA1162519740BRCA
TAMissensep.Q70Lc.209A>T1162521078HNSC
TCMissensep.T492Ac.1474A>G1162519813LUAD
TCSynonymousp.T486Tc.1458A>G1162519829HC