MINDY3
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA101582103215821032+Missense_MutationSNPCCGTCGA-GU-A766-01A-11D-A32B-08TCGA-GU-A766-10A-01D-A329-08g.chr10:15821032C>Gc.1297G>Cc.(1297-1299)Gag>Cagp.E433Q
BLCA101582108015821080+Missense_MutationSNPCCTTCGA-XF-AAN2-01A-11D-A42E-08TCGA-XF-AAN2-10A-01D-A42H-08g.chr10:15821080C>Tc.1249G>Ac.(1249-1251)Gat>Aatp.D417N
BLCA101585886315858863+Missense_MutationSNPCCTTCGA-UY-A9PF-01A-11D-A38G-08TCGA-UY-A9PF-10A-01D-A38J-08g.chr10:15858863C>Tc.853G>Ac.(853-855)Gag>Aagp.E285K
BLCA101586372615863726+Splice_SiteSNPCCTTCGA-CF-A3MI-01A-11D-A20D-08TCGA-CF-A3MI-10A-01D-A20D-08g.chr10:15863726C>Tc.e9-1
BLCA101587563115875631+Missense_MutationSNPAAGTCGA-GV-A3QI-01A-11D-A21Z-08TCGA-GV-A3QI-10A-01D-A21Z-08g.chr10:15875631A>Gc.728T>Cc.(727-729)aTg>aCgp.M243T
BLCA101588357415883574+Missense_MutationSNPCCGTCGA-UY-A78K-01A-11D-A339-08TCGA-UY-A78K-10A-01D-A339-08g.chr10:15883574C>Gc.260G>Cc.(259-261)tGt>tCtp.C87S
BLCA101588357415883574+Missense_MutationSNPCCTTCGA-XF-A9SU-01A-31D-A391-08TCGA-XF-A9SU-10A-01D-A394-08g.chr10:15883574C>Tc.260G>Ac.(259-261)tGt>tAtp.C87Y
BRCA101582863515828635+Missense_MutationSNPCCTTCGA-A8-A095-01A-11W-A019-09TCGA-A8-A095-10A-01W-A021-09g.chr10:15828635C>Tc.1041G>Ac.(1039-1041)atG>atAp.M347I
BRCA101583811415838114+Missense_MutationSNPTTCTCGA-D8-A1XK-01A-21D-A14K-09TCGA-D8-A1XK-10A-01D-A14K-09g.chr10:15838114T>Cc.940A>Gc.(940-942)Acc>Gccp.T314A
BRCA101585887615858876+Nonsense_MutationSNPCCTTCGA-A2-A0SY-01A-31D-A099-09TCGA-A2-A0SY-10A-01D-A099-09g.chr10:15858876C>Tc.840G>Ac.(838-840)tgG>tgAp.W280*
BRCA101587930515879305+Missense_MutationSNPGGCTCGA-GM-A3NW-01A-21D-A228-09TCGA-GM-A3NW-10A-01D-A22A-09g.chr10:15879305G>Cc.474C>Gc.(472-474)ttC>ttGp.F158L
COAD101582420615824206+Missense_MutationSNPGGTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr10:15824206G>Tc.1136C>Ac.(1135-1137)tCt>tAtp.S379Y
COAD101583815115838152+Frame_Shift_InsINS--GTCGA-G4-6309-01A-21D-1835-10TCGA-G4-6309-10A-01D-1835-10g.chr10:15838151_15838152insGc.902_903insCc.(901-903)cctfsp.P301fs
COAD101586367615863676+Missense_MutationSNPCCTTCGA-AA-3952-01A-01W-0995-10TCGA-AA-3952-10A-01W-0995-10g.chr10:15863676C>Tc.780G>Ac.(778-780)atG>atAp.M260I
COAD101587930915879309+Missense_MutationSNPGGATCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:15879309G>Ac.470C>Tc.(469-471)tCg>tTgp.S157L
COADREAD101582420615824206+Missense_MutationSNPGGTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr10:15824206G>Tc.1136C>Ac.(1135-1137)tCt>tAtp.S379Y
COADREAD101583810415838104+Missense_MutationSNPGGATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr10:15838104G>Ac.950C>Tc.(949-951)cCa>cTap.P317L
COADREAD101583815115838152+Frame_Shift_InsINS--GTCGA-G4-6309-01A-21D-1835-10TCGA-G4-6309-10A-01D-1835-10g.chr10:15838151_15838152insGc.902_903insCc.(901-903)cctfsp.P301fs
COADREAD101586367615863676+Missense_MutationSNPCCTTCGA-AA-3952-01A-01W-0995-10TCGA-AA-3952-10A-01W-0995-10g.chr10:15863676C>Tc.780G>Ac.(778-780)atG>atAp.M260I
COADREAD101587930915879309+Missense_MutationSNPGGATCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:15879309G>Ac.470C>Tc.(469-471)tCg>tTgp.S157L
ESCA101587656515876565+Missense_MutationSNPTTCTCGA-R6-A8WC-01A-11D-A37C-09TCGA-R6-A8WC-10A-01D-A37F-09g.chr10:15876565T>Cc.627A>Gc.(625-627)atA>atGp.I209M
GBMLGG101587656015876560+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:15876560G>Tc.632C>Ac.(631-633)cCt>cAtp.P211H
GBMLGG101588522215885222+Missense_MutationSNPCCTTCGA-TM-A84M-01A-11D-A36O-08TCGA-TM-A84M-10A-01D-A367-08g.chr10:15885222C>Tc.224G>Ac.(223-225)cGg>cAgp.R75Q
GBMLGG101590225515902255+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:15902255G>Ac.44C>Tc.(43-45)aCc>aTcp.T15I
HNSC101582859215828592+Missense_MutationSNPCCATCGA-CV-6935-01A-11D-1912-08TCGA-CV-6935-10A-01D-1912-08g.chr10:15828592C>Ac.1084G>Tc.(1084-1086)Ggc>Tgcp.G362C
HNSC101588523115885231+Missense_MutationSNPGGTTCGA-BA-A6DA-01A-31D-A31L-08TCGA-BA-A6DA-10A-01D-A31J-08g.chr10:15885231G>Tc.215C>Ac.(214-216)tCt>tAtp.S72Y
KIPAN101587924315879243+Missense_MutationSNPAAGTCGA-BP-5174-01A-01D-1429-08TCGA-BP-5174-11A-01D-1429-08g.chr10:15879243A>Gc.536T>Cc.(535-537)tTt>tCtp.F179S
KIPAN101590222515902225+Missense_MutationSNPAAGTCGA-CJ-4895-01A-01D-1373-10TCGA-CJ-4895-11A-01D-1373-10g.chr10:15902225A>Gc.74T>Cc.(73-75)aTt>aCtp.I25T
KIRC101587924315879243+Missense_MutationSNPAAGTCGA-BP-5174-01A-01D-1429-08TCGA-BP-5174-11A-01D-1429-08g.chr10:15879243A>Gc.536T>Cc.(535-537)tTt>tCtp.F179S
KIRC101590222515902225+Missense_MutationSNPAAGTCGA-CJ-4895-01A-01D-1373-10TCGA-CJ-4895-11A-01D-1373-10g.chr10:15902225A>Gc.74T>Cc.(73-75)aTt>aCtp.I25T
LGG101587656015876560+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:15876560G>Tc.632C>Ac.(631-633)cCt>cAtp.P211H
LGG101588522215885222+Missense_MutationSNPCCTTCGA-TM-A84M-01A-11D-A36O-08TCGA-TM-A84M-10A-01D-A367-08g.chr10:15885222C>Tc.224G>Ac.(223-225)cGg>cAgp.R75Q
LGG101590225515902255+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:15902255G>Ac.44C>Tc.(43-45)aCc>aTcp.T15I
LIHC101582113815821138+SilentSNPGGTTCGA-EP-A2KA-01A-11D-A183-10TCGA-EP-A2KA-10A-01D-A183-10g.chr10:15821138G>Tc.1191C>Ac.(1189-1191)gtC>gtAp.V397V
LIHC101585883215858832+Splice_SiteSNPAAGTCGA-BC-A10U-01A-11D-A12Z-10TCGA-BC-A10U-11A-11D-A12Z-10g.chr10:15858832A>Gc.e10+1
LIHC101586369615863696+Missense_MutationSNPCCGTCGA-DD-AADF-01A-11D-A40R-10TCGA-DD-AADF-10A-01D-A40U-10g.chr10:15863696C>Gc.760G>Cc.(760-762)Gta>Ctap.V254L
LIHC101587565515875655+Missense_MutationSNPTTCTCGA-DD-AAEK-01A-11D-A40R-10TCGA-DD-AAEK-10A-01D-A40U-10g.chr10:15875655T>Cc.704A>Gc.(703-705)gAt>gGtp.D235G
LIHC101588343215883432+SilentSNPTTCTCGA-EP-A2KB-01A-11D-A183-10TCGA-EP-A2KB-10A-01D-A183-10g.chr10:15883432T>Cc.402A>Gc.(400-402)gaA>gaGp.E134E
LUAD101582101015821010+Missense_MutationSNPCCATCGA-78-8662-01A-11D-2393-08TCGA-78-8662-10A-01D-2393-08g.chr10:15821010C>Ac.1319G>Tc.(1318-1320)cGc>cTcp.R440L
LUAD101582109315821093+SilentSNPGGATCGA-05-4432-01A-01D-1265-08TCGA-05-4432-10A-01D-1265-08g.chr10:15821093G>Ac.1236C>Tc.(1234-1236)ccC>ccTp.P412P
LUAD101587566715875667+Missense_MutationSNPGGATCGA-L4-A4E5-01A-11D-A24P-08TCGA-L4-A4E5-10A-01D-A24P-08g.chr10:15875667G>Ac.692C>Tc.(691-693)tCt>tTtp.S231F
LUAD101587655115876551+Missense_MutationSNPCCTTCGA-55-8092-01A-11D-2238-08TCGA-55-8092-10A-01D-2238-08g.chr10:15876551C>Tc.641G>Ac.(640-642)gGa>gAap.G214E
LUAD101588359915883599+Splice_SiteSNPCCATCGA-50-6594-01A-11D-1753-08TCGA-50-6594-11A-01D-1753-08g.chr10:15883599C>Ac.e4-1
LUSC101588024315880243+Missense_MutationSNPAAGTCGA-56-6545-01A-11D-1817-08TCGA-56-6545-10A-01D-1817-08g.chr10:15880243A>Gc.445T>Cc.(445-447)Ttt>Cttp.F149L
LUSC101588522115885221+SilentSNPCCATCGA-85-6560-01A-11D-1817-08TCGA-85-6560-10A-01D-1817-08g.chr10:15885221C>Ac.225G>Tc.(223-225)cgG>cgTp.R75R
OV101583810815838108+Missense_MutationSNPCCTTCGA-23-2645-01A-01W-1091-09TCGA-23-2645-10A-01W-1091-09g.chr10:15838108C>Tc.946G>Ac.(946-948)Gac>Aacp.D316N
OV101587656815876568+SilentSNPCCTTCGA-13-0793-01A-01W-0370-10TCGA-13-0793-10A-01W-0370-10g.chr10:15876568C>Tc.624G>Ac.(622-624)ttG>ttAp.L208L
PCPG101588345815883458+Missense_MutationSNPGGATCGA-QR-A6H2-01A-11D-A35D-08TCGA-QR-A6H2-10A-01D-A35B-08g.chr10:15883458G>Ac.376C>Tc.(376-378)Cct>Tctp.P126S
PRAD101587927015879270+Missense_MutationSNPTTCTCGA-EJ-7794-01A-11D-2114-08TCGA-EJ-7794-10A-01D-2115-08g.chr10:15879270T>Cc.509A>Gc.(508-510)gAc>gGcp.D170G
READ101583810415838104+Missense_MutationSNPGGATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr10:15838104G>Ac.950C>Tc.(949-951)cCa>cTap.P317L
SARC101590229515902295+Missense_MutationSNPAAGTCGA-DX-AB32-01A-11D-A417-09TCGA-DX-AB32-10A-01D-A41A-09g.chr10:15902295A>Gc.4T>Cc.(4-6)Tcc>Cccp.S2P
SKCM101582420615824206+Missense_MutationSNPGGATCGA-DA-A1HV-06A-21D-A196-08TCGA-DA-A1HV-10A-01D-A198-08g.chr10:15824206G>Ac.1136C>Tc.(1135-1137)tCt>tTtp.S379F
SKCM101582860215828602+SilentSNPGGATCGA-EE-A2GI-06A-11D-A196-08TCGA-EE-A2GI-10A-01D-A198-08g.chr10:15828602G>Ac.1074C>Tc.(1072-1074)atC>atTp.I358I
SKCM101582864015828640+Missense_MutationSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr10:15828640G>Ac.1036C>Tc.(1036-1038)Ctc>Ttcp.L346F
SKCM101583811015838110+Missense_MutationSNPTTATCGA-EE-A29L-06A-12D-A196-08TCGA-EE-A29L-10A-01D-A198-08g.chr10:15838110T>Ac.944A>Tc.(943-945)tAc>tTcp.Y315F
SKCM101585888515858885+SilentSNPGGATCGA-EE-A3J5-06A-11D-A20D-08TCGA-EE-A3J5-10A-01D-A20D-08g.chr10:15858885G>Ac.831C>Tc.(829-831)ttC>ttTp.F277F
SKCM101587930915879309+Missense_MutationSNPGGATCGA-EE-A3AD-06A-11D-A196-08TCGA-EE-A3AD-10A-01D-A198-08g.chr10:15879309G>Ac.470C>Tc.(469-471)tCg>tTgp.S157L
SKCM101587930915879309+Missense_MutationSNPGGATCGA-FS-A4F0-06A-11D-A24R-08TCGA-FS-A4F0-10A-01D-A24R-08g.chr10:15879309G>Ac.470C>Tc.(469-471)tCg>tTgp.S157L
SKCM101588524015885240+Missense_MutationSNPGGATCGA-EE-A2MR-06A-11D-A196-08TCGA-EE-A2MR-10A-01D-A198-08g.chr10:15885240G>Ac.206C>Tc.(205-207)tCg>tTgp.S69L
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN101583812815838128single base substitutionCTexon_variant
BLCA-CN101583812815838128single base substitutionCTmissense_variantR149K446G>A
BLCA-CN101583812815838128single base substitutionCTmissense_variantR14K41G>A
BLCA-CN101583812815838128single base substitutionCTmissense_variantR162K485G>A
BLCA-CN101583812815838128single base substitutionCTmissense_variantR309K926G>A
BLCA-US101586372615863726single base substitutionCTsplice_acceptor_variant
BLCA-US101586372615863726single base substitutionCTupstream_gene_variant
BLCA-US101587563115875631single base substitutionAGmissense_variantM243T728T>C
BLCA-US101587563115875631single base substitutionAGmissense_variantM83T248T>C
BLCA-US101587563115875631single base substitutionAGmissense_variantM96T287T>C
BLCA-US101587563115875631single base substitutionAGsplice_region_variant
BRCA-EU101581521615815216single base substitutionATdownstream_gene_variant
BRCA-EU101581556115815561deletion of <=200bpA-downstream_gene_variant
BRCA-EU101581591615815916single base substitutionATdownstream_gene_variant
BRCA-EU101581762915817629single base substitutionGTdownstream_gene_variant
BRCA-EU101581951515819515single base substitutionAGdownstream_gene_variant
BRCA-EU101581968215819682single base substitutionCAdownstream_gene_variant
BRCA-EU101582021215820212single base substitutionCT3_prime_UTR_variant
BRCA-EU101582021215820212single base substitutionCTdownstream_gene_variant
BRCA-EU101582021215820212single base substitutionCTexon_variant
BRCA-EU101582033915820339single base substitutionTG3_prime_UTR_variant
BRCA-EU101582033915820339single base substitutionTGdownstream_gene_variant
BRCA-EU101582033915820339single base substitutionTGexon_variant
BRCA-EU101582057115820571single base substitutionGT3_prime_UTR_variant
BRCA-EU101582057115820571single base substitutionGTdownstream_gene_variant
BRCA-EU101582057115820571single base substitutionGTexon_variant
BRCA-EU101582078815820788single base substitutionGA3_prime_UTR_variant
BRCA-EU101582078815820788single base substitutionGAdownstream_gene_variant
BRCA-EU101582078815820788single base substitutionGAexon_variant
BRCA-EU101582106515821065single base substitutionTCexon_variant
BRCA-EU101582106515821065single base substitutionTCmissense_variantK127E379A>G
BRCA-EU101582106515821065single base substitutionTCmissense_variantK422E1264A>G
BRCA-EU101582145015821450single base substitutionGAintron_variant
BRCA-EU101582170815821708single base substitutionTAintron_variant
BRCA-EU101582308415823084single base substitutionTAintron_variant
BRCA-EU101582311915823119insertion of <=200bp-ATintron_variant
BRCA-EU101582431815824318single base substitutionCGexon_variant
BRCA-EU101582431815824318single base substitutionCGintron_variant
BRCA-EU101582480815824808single base substitutionGCintron_variant
BRCA-EU101582480815824808single base substitutionGCupstream_gene_variant
BRCA-EU101582545615825456insertion of <=200bp-Tintron_variant
BRCA-EU101582545615825456insertion of <=200bp-Tupstream_gene_variant
BRCA-EU101582569215825692single base substitutionCAintron_variant
BRCA-EU101582569215825692single base substitutionCAupstream_gene_variant
BRCA-EU101582681315826813single base substitutionGAdownstream_gene_variant
BRCA-EU101582681315826813single base substitutionGAintron_variant
BRCA-EU101582681315826813single base substitutionGAupstream_gene_variant
BRCA-EU101582755215827552single base substitutionCAdownstream_gene_variant
BRCA-EU101582755215827552single base substitutionCAintron_variant
BRCA-EU101582755215827552single base substitutionCAupstream_gene_variant
BRCA-EU101582757715827577single base substitutionCTdownstream_gene_variant
BRCA-EU101582757715827577single base substitutionCTintron_variant
BRCA-EU101582757715827577single base substitutionCTupstream_gene_variant
BRCA-EU101582845115828451single base substitutionTCdownstream_gene_variant
BRCA-EU101582845115828451single base substitutionTCintron_variant
BRCA-EU101582845115828451single base substitutionTCupstream_gene_variant
BRCA-EU101582916615829166single base substitutionGCdownstream_gene_variant
BRCA-EU101582916615829166single base substitutionGCintron_variant
BRCA-EU101582916615829166single base substitutionGCupstream_gene_variant
BRCA-EU101583120215831202single base substitutionGA3_prime_UTR_variant
BRCA-EU101583120215831202single base substitutionGAintron_variant
BRCA-EU101583139815831398insertion of <=200bp-Aintron_variant
BRCA-EU101583184515831845deletion of <=200bpA-intron_variant
BRCA-EU101583385615833856single base substitutionTGdownstream_gene_variant
BRCA-EU101583385615833856single base substitutionTGintron_variant
BRCA-EU101583553315835533single base substitutionACdownstream_gene_variant
BRCA-EU101583553315835533single base substitutionACintron_variant
BRCA-EU101583609715836097single base substitutionGCdownstream_gene_variant
BRCA-EU101583609715836097single base substitutionGCintron_variant
BRCA-EU101583741615837416single base substitutionCTdownstream_gene_variant
BRCA-EU101583741615837416single base substitutionCTintron_variant
BRCA-EU101583760315837603single base substitutionCTdownstream_gene_variant
BRCA-EU101583760315837603single base substitutionCTintron_variant
BRCA-EU101583822615838226deletion of <=200bpG-intron_variant
BRCA-EU101583857115838571single base substitutionCTintron_variant
BRCA-EU101583900015839000single base substitutionGTintron_variant
BRCA-EU101584086415840864single base substitutionCTintron_variant
BRCA-EU101584091515840915single base substitutionAGintron_variant
BRCA-EU101584094115840941single base substitutionCTintron_variant
BRCA-EU101584129515841295single base substitutionTCintron_variant
BRCA-EU101584167415841674single base substitutionCAintron_variant
BRCA-EU101584227815842278single base substitutionTGintron_variant
BRCA-EU101584285315842853single base substitutionGTintron_variant
BRCA-EU101584336315843363single base substitutionCAintron_variant
BRCA-EU101584708615847086single base substitutionCGintron_variant
BRCA-EU101584765015847650single base substitutionCAintron_variant
BRCA-EU101584800415848004single base substitutionGAintron_variant
BRCA-EU101584879415848794single base substitutionTCintron_variant
BRCA-EU101584916615849166single base substitutionTCintron_variant
BRCA-EU101584989915849899single base substitutionGAintron_variant
BRCA-EU101585010915850109single base substitutionATintron_variant
BRCA-EU101585024515850245single base substitutionCGintron_variant
BRCA-EU101585063915850639single base substitutionTGintron_variant
BRCA-EU101585065715850657single base substitutionCGintron_variant
BRCA-EU101585076415850764single base substitutionCTintron_variant
BRCA-EU101585194115851941single base substitutionAGintron_variant
BRCA-EU101585326915853269single base substitutionGAintron_variant
BRCA-EU101585607915856079single base substitutionTCintron_variant
BRCA-EU101585636115856361single base substitutionAGintron_variant
BRCA-EU101585658615856586single base substitutionCTintron_variant
BRCA-EU101585781615857816single base substitutionACintron_variant
BRCA-EU101585867215858672single base substitutionCGintron_variant
BRCA-EU101585895615858956single base substitutionAT5_prime_UTR_variant
BRCA-EU101585895615858956single base substitutionATintron_variant
BRCA-EU101586007015860096deletion of <=200bpAGGATTTTAGAGGTGAGCTGTGCAAGT-intron_variant
BRCA-EU101586007015860096deletion of <=200bpAGGATTTTAGAGGTGAGCTGTGCAAGT-upstream_gene_variant
BRCA-EU101586038315860383single base substitutionTAintron_variant
BRCA-EU101586038315860383single base substitutionTAupstream_gene_variant
BRCA-EU101586130915861309single base substitutionGAintron_variant
BRCA-EU101586130915861309single base substitutionGAupstream_gene_variant
BRCA-EU101586392915863929single base substitutionATintron_variant
BRCA-EU101586392915863929single base substitutionATupstream_gene_variant
BRCA-EU101586497115864971single base substitutionGAintron_variant
BRCA-EU101586497115864971single base substitutionGAupstream_gene_variant
BRCA-EU101586509615865096single base substitutionTGintron_variant
BRCA-EU101586593815865938single base substitutionGTintron_variant
BRCA-EU101586705615867056single base substitutionGCintron_variant
BRCA-EU101586761315867613single base substitutionGAintron_variant
BRCA-EU101587011715870117single base substitutionCTintron_variant
BRCA-EU101587138015871380single base substitutionAGintron_variant
BRCA-EU101587156115871561single base substitutionTCintron_variant
BRCA-EU101587413915874139single base substitutionGCintron_variant
BRCA-EU101587461915874619single base substitutionCTintron_variant
BRCA-EU101587572315875723single base substitutionTAintron_variant
BRCA-EU101587607715876077single base substitutionGAintron_variant
BRCA-EU101587707715877077single base substitutionCTintron_variant
BRCA-EU101587790215877902single base substitutionCGintron_variant
BRCA-EU101587840915878409insertion of <=200bp-Tintron_variant
BRCA-EU101587908415879084single base substitutionACintron_variant
BRCA-EU101588047415880474single base substitutionCAintron_variant
BRCA-EU101588047415880474single base substitutionCAupstream_gene_variant
BRCA-EU101588068915880689single base substitutionTCintron_variant
BRCA-EU101588068915880689single base substitutionTCupstream_gene_variant
BRCA-EU101588085915880859single base substitutionCAintron_variant
BRCA-EU101588085915880859single base substitutionCAupstream_gene_variant
BRCA-EU101588202015882020single base substitutionCTintron_variant
BRCA-EU101588202015882020single base substitutionCTupstream_gene_variant
BRCA-EU101588212915882129single base substitutionCTintron_variant
BRCA-EU101588212915882129single base substitutionCTupstream_gene_variant
BRCA-EU101588257015882570single base substitutionCTintron_variant
BRCA-EU101588257015882570single base substitutionCTupstream_gene_variant
BRCA-EU101588385915883859single base substitutionGCintron_variant
BRCA-EU101588385915883859single base substitutionGCupstream_gene_variant
BRCA-EU101588483515884835single base substitutionGCintron_variant
BRCA-EU101588483515884835single base substitutionGCupstream_gene_variant
BRCA-EU101588847615888476single base substitutionCTintron_variant
BRCA-EU101589007615890076single base substitutionCTintron_variant
BRCA-EU101589015215890152single base substitutionCTintron_variant
BRCA-EU101589024115890241single base substitutionGTintron_variant
BRCA-EU101589108615891086single base substitutionAGintron_variant
BRCA-EU101589251815892518single base substitutionGAintron_variant
BRCA-EU101589282115892821single base substitutionCTintron_variant
BRCA-EU101589286615892866single base substitutionCTintron_variant
BRCA-EU101589398415893984single base substitutionCGintron_variant
BRCA-EU101589503115895031single base substitutionGAintron_variant
BRCA-EU101589505515895055single base substitutionGTintron_variant
BRCA-EU101589531615895316deletion of <=200bpG-intron_variant
BRCA-EU101589854015898540single base substitutionCAintron_variant
BRCA-EU101589976715899769deletion of <=200bpAAC-intron_variant
BRCA-EU101589993115899931single base substitutionGAintron_variant
BRCA-EU101590016215900162single base substitutionTCintron_variant
BRCA-EU101590025015900250deletion of <=200bpA-intron_variant
BRCA-EU101590104415901044single base substitutionCGintron_variant
BRCA-EU101590156315901563single base substitutionTGintron_variant
BRCA-EU101590284315902843single base substitutionCTupstream_gene_variant
BRCA-EU101590357215903572single base substitutionCGupstream_gene_variant
BRCA-EU101590370315903703single base substitutionTCupstream_gene_variant
BRCA-EU101590435015904350single base substitutionTGupstream_gene_variant
BRCA-EU101590639015906390single base substitutionCTupstream_gene_variant
BRCA-FR101582845115828451single base substitutionTCdownstream_gene_variant
BRCA-FR101582845115828451single base substitutionTCintron_variant
BRCA-FR101582845115828451single base substitutionTCupstream_gene_variant
BRCA-FR101583385615833856single base substitutionTGdownstream_gene_variant
BRCA-FR101583385615833856single base substitutionTGintron_variant
BRCA-FR101584285315842853single base substitutionGTintron_variant
BRCA-FR101584680715846807single base substitutionGAintron_variant
BRCA-FR101585271815852718single base substitutionGTintron_variant
BRCA-FR101585326915853269single base substitutionGAintron_variant
BRCA-FR101586593815865938single base substitutionGTintron_variant
BRCA-FR101588385915883859single base substitutionGCintron_variant
BRCA-FR101588385915883859single base substitutionGCupstream_gene_variant
BRCA-FR101588878415888784single base substitutionGAintron_variant
BRCA-FR101589108615891086single base substitutionAGintron_variant
BRCA-FR101589251815892518single base substitutionGAintron_variant
BRCA-FR101590488615904886single base substitutionGCupstream_gene_variant
BRCA-UK101584800415848004single base substitutionGAintron_variant
BRCA-UK101585895615858956single base substitutionAT5_prime_UTR_variant
BRCA-UK101585895615858956single base substitutionATintron_variant
BRCA-UK101589854015898540single base substitutionCAintron_variant
BRCA-UK101590478715904787single base substitutionACupstream_gene_variant
BRCA-US101582863515828635single base substitutionCTdownstream_gene_variant
BRCA-US101582863515828635single base substitutionCTexon_variant
BRCA-US101582863515828635single base substitutionCTmissense_variantM347I1041G>A
BRCA-US101582863515828635single base substitutionCTmissense_variantM52I156G>A
BRCA-US101582863515828635single base substitutionCTupstream_gene_variant
BRCA-US101583811415838114single base substitutionTCdownstream_gene_variant
BRCA-US101583811415838114single base substitutionTCexon_variant
BRCA-US101583811415838114single base substitutionTCmissense_variantT154A460A>G
BRCA-US101583811415838114single base substitutionTCmissense_variantT19A55A>G
BRCA-US101583811415838114single base substitutionTCmissense_variantT314A940A>G
BRCA-US101585887615858876single base substitutionCT5_prime_UTR_variant
BRCA-US101585887615858876single base substitutionCTexon_variant
BRCA-US101585887615858876single base substitutionCTstop_gainedW120*360G>A
BRCA-US101585887615858876single base substitutionCTstop_gainedW133*399G>A
BRCA-US101585887615858876single base substitutionCTstop_gainedW280*840G>A
BRCA-US101587930515879305single base substitutionGCexon_variant
BRCA-US101587930515879305single base substitutionGCmissense_variantF11L33C>G
BRCA-US101587930515879305single base substitutionGCmissense_variantF158L474C>G
BRCA-US101587930515879305single base substitutionGCupstream_gene_variant
BTCA-JP101583132815831328deletion of <=200bpA-intron_variant
BTCA-JP101585880815858808deletion of <=200bpA-intron_variant
BTCA-JP101590221215902212single base substitutionCTexon_variant
BTCA-JP101590221215902212single base substitutionCTstop_gainedW29*87G>A
CLLE-ES101583010515830105single base substitutionGTdownstream_gene_variant
CLLE-ES101583010515830105single base substitutionGTintron_variant
COAD-US101582416215824162single base substitutionTCexon_variant
COAD-US101582416215824162single base substitutionTCmissense_variantN394D1180A>G
COAD-US101582416215824162single base substitutionTCmissense_variantN99D295A>G
COAD-US101583815115838151insertion of <=200bp-Gexon_variant
COAD-US101583815115838151insertion of <=200bp-Gframeshift_variantP141P?
COAD-US101583815115838151insertion of <=200bp-Gframeshift_variantP154P?
COAD-US101583815115838151insertion of <=200bp-Gframeshift_variantP301P?
COAD-US101583815115838151insertion of <=200bp-Gframeshift_variantP6P?
COAD-US101587930915879309single base substitutionGAexon_variant
COAD-US101587930915879309single base substitutionGAmissense_variantS10L29C>T
COAD-US101587930915879309single base substitutionGAmissense_variantS157L470C>T
COAD-US101587930915879309single base substitutionGAupstream_gene_variant
COCA-CN101584149215841492single base substitutionAGintron_variant
COCA-CN101584531315845313single base substitutionGAintron_variant
COCA-CN101586357815863578single base substitutionTCintron_variant
COCA-CN101586357815863578single base substitutionTCupstream_gene_variant
COCA-CN101587652615876526single base substitutionGAintron_variant
ESAD-UK101581595715815957single base substitutionCTdownstream_gene_variant
ESAD-UK101581706815817068single base substitutionGTdownstream_gene_variant
ESAD-UK101581709115817091single base substitutionTAdownstream_gene_variant
ESAD-UK101581894315818943single base substitutionACdownstream_gene_variant
ESAD-UK101582096415820964single base substitutionGC3_prime_UTR_variant
ESAD-UK101582096415820964single base substitutionGCexon_variant
ESAD-UK101582113115821131single base substitutionCTexon_variant
ESAD-UK101582113115821131single base substitutionCTmissense_variantV105I313G>A
ESAD-UK101582113115821131single base substitutionCTmissense_variantV400I1198G>A
ESAD-UK101582742615827426insertion of <=200bp-Tdownstream_gene_variant
ESAD-UK101582742615827426insertion of <=200bp-Tintron_variant
ESAD-UK101582742615827426insertion of <=200bp-Tupstream_gene_variant
ESAD-UK101582791915827919single base substitutionATdownstream_gene_variant
ESAD-UK101582791915827919single base substitutionATintron_variant
ESAD-UK101582791915827919single base substitutionATupstream_gene_variant
ESAD-UK101582830315828303single base substitutionTGdownstream_gene_variant
ESAD-UK101582830315828303single base substitutionTGintron_variant
ESAD-UK101582830315828303single base substitutionTGupstream_gene_variant
ESAD-UK101582855115828551single base substitutionCGdownstream_gene_variant
ESAD-UK101582855115828551single base substitutionCGintron_variant
ESAD-UK101582855115828551single base substitutionCGupstream_gene_variant
ESAD-UK101583083615830836single base substitutionTA3_prime_UTR_variant
ESAD-UK101583083615830836single base substitutionTAintron_variant
ESAD-UK101583098615830986single base substitutionTC3_prime_UTR_variant
ESAD-UK101583098615830986single base substitutionTCintron_variant
ESAD-UK101583141815831418single base substitutionATintron_variant
ESAD-UK101583144115831441single base substitutionCTintron_variant
ESAD-UK101583175615831756single base substitutionATintron_variant
ESAD-UK101583315015833150single base substitutionGTdownstream_gene_variant
ESAD-UK101583315015833150single base substitutionGTintron_variant
ESAD-UK101583464915834649single base substitutionCTdownstream_gene_variant
ESAD-UK101583464915834649single base substitutionCTintron_variant
ESAD-UK101583489415834894single base substitutionTGdownstream_gene_variant
ESAD-UK101583489415834894single base substitutionTGintron_variant
ESAD-UK101583499715834997single base substitutionGAdownstream_gene_variant
ESAD-UK101583499715834997single base substitutionGAintron_variant
ESAD-UK101583564315835643single base substitutionGAdownstream_gene_variant
ESAD-UK101583564315835643single base substitutionGAintron_variant
ESAD-UK101583564515835645single base substitutionTGdownstream_gene_variant
ESAD-UK101583564515835645single base substitutionTGintron_variant
ESAD-UK101583590615835906single base substitutionCTdownstream_gene_variant
ESAD-UK101583590615835906single base substitutionCTintron_variant
ESAD-UK101583657815836578single base substitutionGCdownstream_gene_variant
ESAD-UK101583657815836578single base substitutionGCintron_variant
ESAD-UK101583770115837701single base substitutionTCdownstream_gene_variant
ESAD-UK101583770115837701single base substitutionTCintron_variant
ESAD-UK101583983215839832single base substitutionATintron_variant
ESAD-UK101584024715840249deletion of <=200bpGTA-intron_variant
ESAD-UK101584286115842861single base substitutionTCintron_variant
ESAD-UK101584470015844700single base substitutionCTintron_variant
ESAD-UK101584476415844764single base substitutionAGintron_variant
ESAD-UK101584593015845930single base substitutionTGintron_variant
ESAD-UK101584622615846226insertion of <=200bp-Gintron_variant
ESAD-UK101585134215851342single base substitutionACintron_variant
ESAD-UK101585277415852774single base substitutionATintron_variant
ESAD-UK101585398715853987single base substitutionTGintron_variant
ESAD-UK101585445515854455single base substitutionTCintron_variant
ESAD-UK101585721115857211deletion of <=200bpT-intron_variant
ESAD-UK101586007915860079single base substitutionGAintron_variant
ESAD-UK101586007915860079single base substitutionGAupstream_gene_variant
ESAD-UK101586086215860862single base substitutionGCintron_variant
ESAD-UK101586086215860862single base substitutionGCupstream_gene_variant
ESAD-UK101586212015862120single base substitutionCTintron_variant
ESAD-UK101586212015862120single base substitutionCTupstream_gene_variant
ESAD-UK101586334015863340single base substitutionTGintron_variant
ESAD-UK101586334015863340single base substitutionTGupstream_gene_variant
ESAD-UK101586568015865680single base substitutionCGintron_variant
ESAD-UK101586695315866953single base substitutionGCintron_variant
ESAD-UK101586710715867107single base substitutionAGintron_variant
ESAD-UK101586785115867851single base substitutionATintron_variant
ESAD-UK101586788715867887single base substitutionTGintron_variant
ESAD-UK101586877715868777single base substitutionCTintron_variant
ESAD-UK101586940515869405single base substitutionTCintron_variant
ESAD-UK101586963515869635single base substitutionGCintron_variant
ESAD-UK101587102615871026single base substitutionGCintron_variant
ESAD-UK101587523415875234single base substitutionACintron_variant
ESAD-UK101587587715875877single base substitutionATintron_variant
ESAD-UK101587680015876801deletion of <=200bpTT-intron_variant
ESAD-UK101587690315876903single base substitutionGTintron_variant
ESAD-UK101587690615876906single base substitutionGAintron_variant
ESAD-UK101587747215877472single base substitutionGTintron_variant
ESAD-UK101587938115879381single base substitutionACintron_variant
ESAD-UK101587938115879381single base substitutionACupstream_gene_variant
ESAD-UK101587938315879383single base substitutionAGintron_variant
ESAD-UK101587938315879383single base substitutionAGupstream_gene_variant
ESAD-UK101588089315880893single base substitutionCTintron_variant
ESAD-UK101588089315880893single base substitutionCTupstream_gene_variant
ESAD-UK101588127915881279single base substitutionCGintron_variant
ESAD-UK101588127915881279single base substitutionCGupstream_gene_variant
ESAD-UK101588438415884392deletion of <=200bpAGTGAATAT-intron_variant
ESAD-UK101588438415884392deletion of <=200bpAGTGAATAT-upstream_gene_variant
ESAD-UK101588555415885554single base substitutionGAintron_variant
ESAD-UK101588595615885956single base substitutionTCintron_variant
ESAD-UK101588617315886173single base substitutionTCintron_variant
ESAD-UK101588687815886878single base substitutionCAintron_variant
ESAD-UK101588729315887293single base substitutionGAintron_variant
ESAD-UK101589124015891240single base substitutionTCintron_variant
ESAD-UK101589253915892539single base substitutionATintron_variant
ESAD-UK101589392515893925single base substitutionCTintron_variant
ESAD-UK101589428715894287single base substitutionAGintron_variant
ESAD-UK101589486215894862single base substitutionGTintron_variant
ESAD-UK101589699315896993single base substitutionTCintron_variant
ESAD-UK101589897115899007deletion of <=200bpACAGCAGGCAGATCAGTCCTTTAAAAACTTGTCAAGT-intron_variant
ESAD-UK101589967515899675single base substitutionACintron_variant
ESAD-UK101589999415899994deletion of <=200bpA-intron_variant
ESAD-UK101590050715900507single base substitutionCTintron_variant
ESAD-UK101590097115900971single base substitutionGAintron_variant
ESAD-UK101590180815901808single base substitutionGAintron_variant
ESAD-UK101590201015902010single base substitutionGTintron_variant
ESAD-UK101590303315903033single base substitutionTAupstream_gene_variant
ESAD-UK101590311515903115single base substitutionGAupstream_gene_variant
ESAD-UK101590418115904181single base substitutionCTupstream_gene_variant
ESAD-UK101590476815904768single base substitutionTCupstream_gene_variant
ESAD-UK101590579815905798single base substitutionACupstream_gene_variant
ESAD-UK101590662715906627single base substitutionTCupstream_gene_variant
ESCA-CN101587567915875679deletion of <=200bpC-exon_variant
ESCA-CN101587567915875679deletion of <=200bpC-frameshift_variantG227
ESCA-CN101587567915875679deletion of <=200bpC-frameshift_variantG67
ESCA-CN101587567915875679deletion of <=200bpC-frameshift_variantG80
KIRC-US101587924315879243single base substitutionAGexon_variant
KIRC-US101587924315879243single base substitutionAGmissense_variantF179S536T>C
KIRC-US101587924315879243single base substitutionAGmissense_variantF19S56T>C
KIRC-US101587924315879243single base substitutionAGmissense_variantF32S95T>C
KIRC-US101588026215880262single base substitutionTA5_prime_UTR_premature_start_codon_gain_variant
KIRC-US101588026215880262single base substitutionTAintron_variant
KIRC-US101588026215880262single base substitutionTAmissense_variantE142D426A>T
KIRC-US101588026215880262single base substitutionTAupstream_gene_variant
KIRC-US101590222515902225single base substitutionAGexon_variant
KIRC-US101590222515902225single base substitutionAGmissense_variantI25T74T>C
LAML-KR101585825915858259single base substitutionCAintron_variant
LAML-KR101588874115888741single base substitutionGTintron_variant
LICA-FR101581675215816752single base substitutionTAdownstream_gene_variant
LICA-FR101582206415822064single base substitutionTCintron_variant
LICA-FR101583814615838146single base substitutionGAexon_variant
LICA-FR101583814615838146single base substitutionGAmissense_variantA143V428C>T
LICA-FR101583814615838146single base substitutionGAmissense_variantA156V467C>T
LICA-FR101583814615838146single base substitutionGAmissense_variantA303V908C>T
LICA-FR101583814615838146single base substitutionGAmissense_variantA8V23C>T
LICA-FR101584046415840464insertion of <=200bp-Tintron_variant
LICA-FR101585344615853446single base substitutionCTintron_variant
LICA-FR101585589815855898single base substitutionAGintron_variant
LICA-FR101587115915871159single base substitutionATintron_variant
LICA-FR101588387115883871single base substitutionTGintron_variant
LICA-FR101588387115883871single base substitutionTGupstream_gene_variant
LICA-FR101589802115898021single base substitutionAGintron_variant
LIHC-US101585883215858832single base substitutionAGsplice_donor_variant
LIHC-US101587661215876612single base substitutionTCexon_variant
LIHC-US101587661215876612single base substitutionTCmissense_variantI194V580A>G
LIHC-US101587661215876612single base substitutionTCmissense_variantI34V100A>G
LIHC-US101587661215876612single base substitutionTCmissense_variantI47V139A>G
LIHC-US101588343215883432single base substitutionTCexon_variant
LIHC-US101588343215883432single base substitutionTCsynonymous_variantE134E402A>G
LIHC-US101588343215883432single base substitutionTCupstream_gene_variant
LINC-JP101581882915818829single base substitutionACdownstream_gene_variant
LINC-JP101582433815824338single base substitutionTGintron_variant
LINC-JP101582433815824338single base substitutionTGupstream_gene_variant
LINC-JP101585196115851961single base substitutionTCintron_variant
LINC-JP101585471115854711single base substitutionCAintron_variant
LINC-JP101585879915858799single base substitutionTCintron_variant
LINC-JP101585889115858891single base substitutionTC5_prime_UTR_variant
LINC-JP101585889115858891single base substitutionTCexon_variant
LINC-JP101585889115858891single base substitutionTCsynonymous_variantP115P345A>G
LINC-JP101585889115858891single base substitutionTCsynonymous_variantP128P384A>G
LINC-JP101585889115858891single base substitutionTCsynonymous_variantP275P825A>G
LINC-JP101586262815862628single base substitutionGTintron_variant
LINC-JP101586262815862628single base substitutionGTupstream_gene_variant
LINC-JP101587499715874997single base substitutionACintron_variant
LINC-JP101587944515879445single base substitutionCAintron_variant
LINC-JP101587944515879445single base substitutionCAupstream_gene_variant
LINC-JP101588117615881176deletion of <=200bpA-intron_variant
LINC-JP101588117615881176deletion of <=200bpA-upstream_gene_variant
LINC-JP101588654415886544single base substitutionAGintron_variant
LINC-JP101588992615889926single base substitutionTCexon_variant
LINC-JP101588992615889926single base substitutionTCsynonymous_variantE37E111A>G
LINC-JP101590249515902495single base substitutionCA5_prime_UTR_premature_start_codon_gain_variant
LINC-JP101590249515902495single base substitutionCAexon_variant
LINC-JP101590266415902664single base substitutionTCupstream_gene_variant
LIRI-JP101581572515815725single base substitutionGCdownstream_gene_variant
LIRI-JP101581619215816192single base substitutionCAdownstream_gene_variant
LIRI-JP101581656415816564single base substitutionCTdownstream_gene_variant
LIRI-JP101581764315817643single base substitutionTCdownstream_gene_variant
LIRI-JP101581865015818650single base substitutionTCdownstream_gene_variant
LIRI-JP101581956615819567deletion of <=200bpTT-downstream_gene_variant
LIRI-JP101581973115819731single base substitutionAGdownstream_gene_variant
LIRI-JP101582015115820151single base substitutionTCdownstream_gene_variant
LIRI-JP101582036615820366single base substitutionTG3_prime_UTR_variant
LIRI-JP101582036615820366single base substitutionTGdownstream_gene_variant
LIRI-JP101582036615820366single base substitutionTGexon_variant
LIRI-JP101582155515821555single base substitutionTCintron_variant
LIRI-JP101582156515821565single base substitutionAGintron_variant
LIRI-JP101582223415822234single base substitutionCAintron_variant
LIRI-JP101582488015824880single base substitutionACintron_variant
LIRI-JP101582488015824880single base substitutionACupstream_gene_variant
LIRI-JP101582621215826212single base substitutionATdownstream_gene_variant
LIRI-JP101582621215826212single base substitutionATintron_variant
LIRI-JP101582621215826212single base substitutionATupstream_gene_variant
LIRI-JP101582759115827591single base substitutionAGdownstream_gene_variant
LIRI-JP101582759115827591single base substitutionAGintron_variant
LIRI-JP101582759115827591single base substitutionAGupstream_gene_variant
LIRI-JP101582921715829217single base substitutionTCdownstream_gene_variant
LIRI-JP101582921715829217single base substitutionTCintron_variant
LIRI-JP101582921715829217single base substitutionTCupstream_gene_variant
LIRI-JP101583149115831491single base substitutionTCintron_variant
LIRI-JP101583439215834392single base substitutionGTdownstream_gene_variant
LIRI-JP101583439215834392single base substitutionGTintron_variant
LIRI-JP101583545115835451single base substitutionGCdownstream_gene_variant
LIRI-JP101583545115835451single base substitutionGCintron_variant
LIRI-JP101583657415836574single base substitutionTCdownstream_gene_variant
LIRI-JP101583657415836574single base substitutionTCintron_variant
LIRI-JP101583981315839813single base substitutionTCintron_variant
LIRI-JP101584083315840833single base substitutionTCintron_variant
LIRI-JP101584120415841204single base substitutionTCintron_variant
LIRI-JP101584147215841472single base substitutionAGintron_variant
LIRI-JP101584213415842134single base substitutionTCintron_variant
LIRI-JP101584371315843713single base substitutionTCintron_variant
LIRI-JP101584489415844894single base substitutionTCintron_variant
LIRI-JP101584564715845647single base substitutionTGintron_variant
LIRI-JP101584690615846906single base substitutionGTintron_variant
LIRI-JP101584907515849075single base substitutionTGintron_variant
LIRI-JP101585165215851652single base substitutionTCintron_variant
LIRI-JP101585371815853718single base substitutionTAintron_variant
LIRI-JP101585553315855533single base substitutionTCintron_variant
LIRI-JP101585589915855899single base substitutionCGintron_variant
LIRI-JP101585621715856217single base substitutionGCintron_variant
LIRI-JP101585663915856639single base substitutionTCintron_variant
LIRI-JP101585700715857007single base substitutionTCintron_variant
LIRI-JP101585860915858611deletion of <=200bpAAG-intron_variant
LIRI-JP101585911415859114single base substitutionTC5_prime_UTR_premature_start_codon_gain_variant
LIRI-JP101585911415859114single base substitutionTCintron_variant
LIRI-JP101585963215859632single base substitutionAG5_prime_UTR_variant
LIRI-JP101585963215859632single base substitutionAGintron_variant
LIRI-JP101586108615861089deletion of <=200bpGGAG-intron_variant
LIRI-JP101586108615861089deletion of <=200bpGGAG-upstream_gene_variant
LIRI-JP101586109315861093single base substitutionGAintron_variant
LIRI-JP101586109315861093single base substitutionGAupstream_gene_variant
LIRI-JP101586327115863271single base substitutionCTintron_variant
LIRI-JP101586327115863271single base substitutionCTupstream_gene_variant
LIRI-JP101586380215863802single base substitutionTCintron_variant
LIRI-JP101586380215863802single base substitutionTCupstream_gene_variant
LIRI-JP101586479415864794single base substitutionGTintron_variant
LIRI-JP101586479415864794single base substitutionGTupstream_gene_variant
LIRI-JP101586681015866810single base substitutionTCintron_variant
LIRI-JP101586734015867340single base substitutionTCintron_variant
LIRI-JP101586842915868429single base substitutionCTintron_variant
LIRI-JP101586878615868786single base substitutionTCintron_variant
LIRI-JP101587014615870146single base substitutionCGintron_variant
LIRI-JP101587020115870201single base substitutionGTintron_variant
LIRI-JP101587037315870373single base substitutionTAintron_variant
LIRI-JP101587243515872435single base substitutionTCintron_variant
LIRI-JP101587327715873277single base substitutionTCintron_variant
LIRI-JP101587344415873444deletion of <=200bpC-intron_variant
LIRI-JP101587473015874730single base substitutionAGintron_variant
LIRI-JP101587730815877308single base substitutionGTintron_variant
LIRI-JP101587849415878494single base substitutionCAintron_variant
LIRI-JP101588341715883417single base substitutionTCsplice_region_variant
LIRI-JP101588341715883417single base substitutionTCupstream_gene_variant
LIRI-JP101588434715884347single base substitutionTCintron_variant
LIRI-JP101588434715884347single base substitutionTCupstream_gene_variant
LIRI-JP101588815715888157single base substitutionACintron_variant
LIRI-JP101588815715888157single base substitutionAGintron_variant
LIRI-JP101588833615888336single base substitutionGAintron_variant
LIRI-JP101588941515889415single base substitutionTAintron_variant
LIRI-JP101588975215889752single base substitutionTCintron_variant
LIRI-JP101589020215890202single base substitutionTCintron_variant
LIRI-JP101589170015891700single base substitutionAGintron_variant
LIRI-JP101589218415892184single base substitutionTCintron_variant
LIRI-JP101589469415894694single base substitutionCTintron_variant
LIRI-JP101589580215895802single base substitutionTCintron_variant
LIRI-JP101589647615896476single base substitutionATintron_variant
LIRI-JP101589707615897076single base substitutionTCintron_variant
LIRI-JP101590075615900756single base substitutionTCintron_variant
LIRI-JP101590096115900961single base substitutionTCintron_variant
LIRI-JP101590142715901427single base substitutionTCintron_variant
LIRI-JP101590541115905411single base substitutionAGupstream_gene_variant
LIRI-JP101590591715905917single base substitutionGCupstream_gene_variant
LUSC-KR101581875415818754single base substitutionGAdownstream_gene_variant
LUSC-KR101581960015819600single base substitutionTCdownstream_gene_variant
LUSC-KR101582594015825940single base substitutionCAdownstream_gene_variant
LUSC-KR101582594015825940single base substitutionCAintron_variant
LUSC-KR101582594015825940single base substitutionCAupstream_gene_variant
LUSC-KR101582709315827093single base substitutionGCdownstream_gene_variant
LUSC-KR101582709315827093single base substitutionGCintron_variant
LUSC-KR101582709315827093single base substitutionGCupstream_gene_variant
LUSC-KR101582972615829726single base substitutionCAdownstream_gene_variant
LUSC-KR101582972615829726single base substitutionCAintron_variant
LUSC-KR101583032615830326single base substitutionCAdownstream_gene_variant
LUSC-KR101583032615830326single base substitutionCAintron_variant
LUSC-KR101583079715830797single base substitutionCTdownstream_gene_variant
LUSC-KR101583079715830797single base substitutionCTintron_variant
LUSC-KR101583275815832758single base substitutionCAintron_variant
LUSC-KR101583797715837977single base substitutionACdownstream_gene_variant
LUSC-KR101583797715837977single base substitutionACintron_variant
LUSC-KR101583941215839412single base substitutionTGintron_variant
LUSC-KR101583991515839915single base substitutionCTintron_variant
LUSC-KR101584165115841651single base substitutionGCintron_variant
LUSC-KR101584639915846399single base substitutionCGintron_variant
LUSC-KR101585260915852609single base substitutionACintron_variant
LUSC-KR101585566915855669single base substitutionGCintron_variant
LUSC-KR101585675915856759single base substitutionAGintron_variant
LUSC-KR101585867015858670single base substitutionCGintron_variant
LUSC-KR101585880115858801single base substitutionAGintron_variant
LUSC-KR101586147015861470single base substitutionCGintron_variant
LUSC-KR101586147015861470single base substitutionCGupstream_gene_variant
LUSC-KR101586378315863783single base substitutionTCintron_variant
LUSC-KR101586378315863783single base substitutionTCupstream_gene_variant
LUSC-KR101586612915866129single base substitutionTAintron_variant
LUSC-KR101586713315867133single base substitutionTCintron_variant
LUSC-KR101586935615869356single base substitutionCTintron_variant
LUSC-KR101587568815875688single base substitutionATexon_variant
LUSC-KR101587568815875688single base substitutionATmissense_variantL224Q671T>A
LUSC-KR101587568815875688single base substitutionATmissense_variantL64Q191T>A
LUSC-KR101587568815875688single base substitutionATmissense_variantL77Q230T>A
LUSC-KR101587838815878388single base substitutionACintron_variant
LUSC-KR101588026615880266single base substitutionAT5_prime_UTR_variant
LUSC-KR101588026615880266single base substitutionATintron_variant
LUSC-KR101588026615880266single base substitutionATmissense_variantV141D422T>A
LUSC-KR101588026615880266single base substitutionATupstream_gene_variant
LUSC-KR101588483515884835single base substitutionGAintron_variant
LUSC-KR101588483515884835single base substitutionGAupstream_gene_variant
LUSC-KR101588627115886271single base substitutionTAintron_variant
LUSC-KR101588670015886700single base substitutionCGintron_variant
LUSC-KR101589507215895072single base substitutionCTintron_variant
LUSC-KR101590275215902752single base substitutionGTupstream_gene_variant
LUSC-KR101590347415903474single base substitutionTAupstream_gene_variant
LUSC-KR101590550115905501single base substitutionATupstream_gene_variant
LUSC-US101588024315880243single base substitutionAG5_prime_UTR_variant
LUSC-US101588024315880243single base substitutionAGintron_variant
LUSC-US101588024315880243single base substitutionAGmissense_variantF149L445T>C
LUSC-US101588024315880243single base substitutionAGupstream_gene_variant
LUSC-US101588522115885221single base substitutionCAexon_variant
LUSC-US101588522115885221single base substitutionCAsynonymous_variantR75R225G>T
LUSC-US101588522115885221single base substitutionCAupstream_gene_variant
MALY-DE101581870715818708deletion of <=200bpTG-downstream_gene_variant
MALY-DE101582401015824010single base substitutionCAintron_variant
MALY-DE101584371515843715single base substitutionACintron_variant
MALY-DE101584372015843720single base substitutionACintron_variant
MALY-DE101584515115845151single base substitutionGAintron_variant
MALY-DE101585176015851760single base substitutionATintron_variant
MALY-DE101585822815858228single base substitutionCTintron_variant
MALY-DE101586032915860329single base substitutionCTintron_variant
MALY-DE101586032915860329single base substitutionCTupstream_gene_variant
MALY-DE101586670715866707single base substitutionCTintron_variant
MALY-DE101588321915883219insertion of <=200bp-Tintron_variant
MALY-DE101588321915883219insertion of <=200bp-Tupstream_gene_variant
MALY-DE101589528515895285single base substitutionCTintron_variant
MALY-DE101589856915898569single base substitutionTCintron_variant
MALY-DE101590261015902610single base substitutionACupstream_gene_variant
MALY-DE101590261615902616single base substitutionGAupstream_gene_variant
MALY-DE101590556815905568single base substitutionTCupstream_gene_variant
MELA-AU101581555215815552single base substitutionTCdownstream_gene_variant
MELA-AU101581584315815843single base substitutionGAdownstream_gene_variant
MELA-AU101581584915815849single base substitutionGAdownstream_gene_variant
MELA-AU101581592015815920single base substitutionGAdownstream_gene_variant
MELA-AU101581656315816563single base substitutionTGdownstream_gene_variant
MELA-AU101581666015816660single base substitutionAGdownstream_gene_variant
MELA-AU101581706115817061single base substitutionGAdownstream_gene_variant
MELA-AU101581725015817250single base substitutionCTdownstream_gene_variant
MELA-AU101581753215817532single base substitutionGAdownstream_gene_variant
MELA-AU101581771715817717single base substitutionTCdownstream_gene_variant
MELA-AU101581805915818059single base substitutionTCdownstream_gene_variant
MELA-AU101581814415818144single base substitutionTCdownstream_gene_variant
MELA-AU101581848915818489single base substitutionGAdownstream_gene_variant
MELA-AU101581877915818779single base substitutionGAdownstream_gene_variant
MELA-AU101581878415818784single base substitutionTAdownstream_gene_variant
MELA-AU101581925415819254single base substitutionGAdownstream_gene_variant
MELA-AU101581949315819493single base substitutionGAdownstream_gene_variant
MELA-AU101581954615819546single base substitutionAGdownstream_gene_variant
MELA-AU101581991015819910single base substitutionACdownstream_gene_variant
MELA-AU101582003315820033single base substitutionAGdownstream_gene_variant
MELA-AU101582003615820036single base substitutionGCdownstream_gene_variant
MELA-AU101582042715820427single base substitutionGA3_prime_UTR_variant
MELA-AU101582042715820427single base substitutionGAdownstream_gene_variant
MELA-AU101582042715820427single base substitutionGAexon_variant
MELA-AU101582066415820664single base substitutionTC3_prime_UTR_variant
MELA-AU101582066415820664single base substitutionTCdownstream_gene_variant
MELA-AU101582066415820664single base substitutionTCexon_variant
MELA-AU101582163915821639single base substitutionGAintron_variant
MELA-AU101582348515823485single base substitutionGAintron_variant
MELA-AU101582357315823573single base substitutionGAintron_variant
MELA-AU101582437015824370single base substitutionGAintron_variant
MELA-AU101582437015824370single base substitutionGAupstream_gene_variant
MELA-AU101582467115824671single base substitutionGAintron_variant
MELA-AU101582467115824671single base substitutionGAupstream_gene_variant
MELA-AU101582478615824786single base substitutionGAintron_variant
MELA-AU101582478615824786single base substitutionGAupstream_gene_variant
MELA-AU101582676015826760single base substitutionGAdownstream_gene_variant
MELA-AU101582676015826760single base substitutionGAintron_variant
MELA-AU101582676015826760single base substitutionGAupstream_gene_variant
MELA-AU101582728915827289single base substitutionGAdownstream_gene_variant
MELA-AU101582728915827289single base substitutionGAintron_variant
MELA-AU101582728915827289single base substitutionGAupstream_gene_variant
MELA-AU101582735015827351multiple base substitution (>=2bp and <=200bp)CTTCdownstream_gene_variant
MELA-AU101582735015827351multiple base substitution (>=2bp and <=200bp)CTTCintron_variant
MELA-AU101582735015827351multiple base substitution (>=2bp and <=200bp)CTTCupstream_gene_variant
MELA-AU101582787815827878single base substitutionGAdownstream_gene_variant
MELA-AU101582787815827878single base substitutionGAintron_variant
MELA-AU101582787815827878single base substitutionGAupstream_gene_variant
MELA-AU101582812515828125single base substitutionGAdownstream_gene_variant
MELA-AU101582812515828125single base substitutionGAintron_variant
MELA-AU101582812515828125single base substitutionGAupstream_gene_variant
MELA-AU101582814715828147single base substitutionGAdownstream_gene_variant
MELA-AU101582814715828147single base substitutionGAintron_variant
MELA-AU101582814715828147single base substitutionGAupstream_gene_variant
MELA-AU101582903315829033single base substitutionCTdownstream_gene_variant
MELA-AU101582903315829033single base substitutionCTintron_variant
MELA-AU101582903315829033single base substitutionCTupstream_gene_variant
MELA-AU101582977415829774single base substitutionGAdownstream_gene_variant
MELA-AU101582977415829774single base substitutionGAintron_variant
MELA-AU101583010115830101single base substitutionCTdownstream_gene_variant
MELA-AU101583010115830101single base substitutionCTintron_variant
MELA-AU101583085015830850single base substitutionGA3_prime_UTR_variant
MELA-AU101583085015830850single base substitutionGAintron_variant
MELA-AU101583260715832607single base substitutionGAintron_variant
MELA-AU101583292115832921single base substitutionAGintron_variant
MELA-AU101583381015833810single base substitutionGAdownstream_gene_variant
MELA-AU101583381015833810single base substitutionGAintron_variant
MELA-AU101583383415833834single base substitutionGAdownstream_gene_variant
MELA-AU101583383415833834single base substitutionGAintron_variant
MELA-AU101583418215834182single base substitutionGAdownstream_gene_variant
MELA-AU101583418215834182single base substitutionGAintron_variant
MELA-AU101583454515834545single base substitutionGAdownstream_gene_variant
MELA-AU101583454515834545single base substitutionGAintron_variant
MELA-AU101583455515834555single base substitutionGAdownstream_gene_variant
MELA-AU101583455515834555single base substitutionGAintron_variant
MELA-AU101583541815835418single base substitutionCTdownstream_gene_variant
MELA-AU101583541815835418single base substitutionCTintron_variant
MELA-AU101583644315836443single base substitutionGAdownstream_gene_variant
MELA-AU101583644315836443single base substitutionGAintron_variant
MELA-AU101583683715836837single base substitutionTCdownstream_gene_variant
MELA-AU101583683715836837single base substitutionTCintron_variant
MELA-AU101583686815836868single base substitutionGAdownstream_gene_variant
MELA-AU101583686815836868single base substitutionGAintron_variant
MELA-AU101583781415837814single base substitutionATdownstream_gene_variant
MELA-AU101583781415837814single base substitutionATintron_variant
MELA-AU101583807615838076single base substitutionGAdownstream_gene_variant
MELA-AU101583807615838076single base substitutionGAintron_variant
MELA-AU101583811015838110single base substitutionTAdownstream_gene_variant
MELA-AU101583811015838110single base substitutionTAexon_variant
MELA-AU101583811015838110single base substitutionTAmissense_variantY155F464A>T
MELA-AU101583811015838110single base substitutionTAmissense_variantY20F59A>T
MELA-AU101583811015838110single base substitutionTAmissense_variantY315F944A>T
MELA-AU101583823315838233single base substitutionGAintron_variant
MELA-AU101583855315838553single base substitutionGAintron_variant
MELA-AU101583911215839112single base substitutionCTintron_variant
MELA-AU101583914515839145single base substitutionTGintron_variant
MELA-AU101583948715839487single base substitutionCTintron_variant
MELA-AU101583965115839651single base substitutionGAintron_variant
MELA-AU101583986015839860single base substitutionCGintron_variant
MELA-AU101584002515840025single base substitutionGAintron_variant
MELA-AU101584011915840119single base substitutionGAintron_variant
MELA-AU101584019415840194single base substitutionGAintron_variant
MELA-AU101584039115840391single base substitutionGAintron_variant
MELA-AU101584052815840528single base substitutionGAintron_variant
MELA-AU101584194815841948single base substitutionGAintron_variant
MELA-AU101584205615842056single base substitutionGAintron_variant
MELA-AU101584237015842370single base substitutionAGintron_variant
MELA-AU101584287615842876single base substitutionTCintron_variant
MELA-AU101584292115842921single base substitutionAGintron_variant
MELA-AU101584325115843251single base substitutionGAintron_variant
MELA-AU101584409915844099single base substitutionGAintron_variant
MELA-AU101584419115844191single base substitutionGAintron_variant
MELA-AU101584435615844356single base substitutionGAintron_variant
MELA-AU101584468415844684single base substitutionGAintron_variant
MELA-AU101584676015846760single base substitutionAGintron_variant
MELA-AU101584805615848056single base substitutionGAintron_variant
MELA-AU101584948015849480single base substitutionCTintron_variant
MELA-AU101585016015850160single base substitutionCTintron_variant
MELA-AU101585020415850204single base substitutionGAintron_variant
MELA-AU101585022815850228single base substitutionTGintron_variant
MELA-AU101585112315851123single base substitutionTAintron_variant
MELA-AU101585119115851191single base substitutionGAintron_variant
MELA-AU101585260615852606single base substitutionACintron_variant
MELA-AU101585314415853144single base substitutionGAintron_variant
MELA-AU101585340515853405single base substitutionGAintron_variant
MELA-AU101585375615853758deletion of <=200bpTTA-intron_variant
MELA-AU101585449815854498single base substitutionGAintron_variant
MELA-AU101585569615855696single base substitutionAGintron_variant
MELA-AU101585591615855916single base substitutionATintron_variant
MELA-AU101585610015856100single base substitutionGAintron_variant
MELA-AU101585672015856720single base substitutionGAintron_variant
MELA-AU101585902315859023single base substitutionGA5_prime_UTR_variant
MELA-AU101585902315859023single base substitutionGAintron_variant
MELA-AU101586025415860254single base substitutionGAintron_variant
MELA-AU101586025415860254single base substitutionGAupstream_gene_variant
MELA-AU101586061515860615insertion of <=200bp-Gintron_variant
MELA-AU101586061515860615insertion of <=200bp-Gupstream_gene_variant
MELA-AU101586081215860812single base substitutionGAintron_variant
MELA-AU101586081215860812single base substitutionGAupstream_gene_variant
MELA-AU101586220315862203single base substitutionGCintron_variant
MELA-AU101586220315862203single base substitutionGCupstream_gene_variant
MELA-AU101586271515862715single base substitutionGAintron_variant
MELA-AU101586271515862715single base substitutionGAupstream_gene_variant
MELA-AU101586318615863186single base substitutionGAintron_variant
MELA-AU101586318615863186single base substitutionGAupstream_gene_variant
MELA-AU101586343515863435single base substitutionCAintron_variant
MELA-AU101586343515863435single base substitutionCAupstream_gene_variant
MELA-AU101586493215864932single base substitutionTCintron_variant
MELA-AU101586493215864932single base substitutionTCupstream_gene_variant
MELA-AU101586538815865388single base substitutionATintron_variant
MELA-AU101586597415865974single base substitutionGAintron_variant
MELA-AU101586657515866575single base substitutionGAintron_variant
MELA-AU101586683115866831single base substitutionAGintron_variant
MELA-AU101586734115867341single base substitutionGAintron_variant
MELA-AU101586976715869767single base substitutionGAintron_variant
MELA-AU101587071815870718single base substitutionGAintron_variant
MELA-AU101587116415871164single base substitutionGAintron_variant
MELA-AU101587240015872400single base substitutionAGintron_variant
MELA-AU101587283415872834single base substitutionGAintron_variant
MELA-AU101587316015873160single base substitutionGAintron_variant
MELA-AU101587331015873310single base substitutionGAintron_variant
MELA-AU101587371915873719single base substitutionGAintron_variant
MELA-AU101587503415875034single base substitutionGAintron_variant
MELA-AU101587507115875071single base substitutionGAintron_variant
MELA-AU101587507515875075single base substitutionGAintron_variant
MELA-AU101587507615875076single base substitutionGAintron_variant
MELA-AU101587513415875134single base substitutionGAintron_variant
MELA-AU101587565015875650single base substitutionCTexon_variant
MELA-AU101587565015875650single base substitutionCTmissense_variantD237N709G>A
MELA-AU101587565015875650single base substitutionCTmissense_variantD77N229G>A
MELA-AU101587565015875650single base substitutionCTmissense_variantD90N268G>A
MELA-AU101587628115876281single base substitutionTCintron_variant
MELA-AU101587659415876594single base substitutionCTexon_variant
MELA-AU101587659415876594single base substitutionCTmissense_variantE200K598G>A
MELA-AU101587659415876594single base substitutionCTmissense_variantE40K118G>A
MELA-AU101587659415876594single base substitutionCTmissense_variantE53K157G>A
MELA-AU101587698415876984single base substitutionCTintron_variant
MELA-AU101587705015877050single base substitutionATintron_variant
MELA-AU101587716215877162single base substitutionGAintron_variant
MELA-AU101587727315877273single base substitutionAGintron_variant
MELA-AU101587893615878936single base substitutionGAintron_variant
MELA-AU101587894415878944single base substitutionGAintron_variant
MELA-AU101587895715878957single base substitutionGAintron_variant
MELA-AU101587902815879028single base substitutionCAintron_variant
MELA-AU101587914715879147single base substitutionATintron_variant
MELA-AU101587943715879438multiple base substitution (>=2bp and <=200bp)GGACintron_variant
MELA-AU101587943715879438multiple base substitution (>=2bp and <=200bp)GGACupstream_gene_variant
MELA-AU101587949115879491single base substitutionCTintron_variant
MELA-AU101587949115879491single base substitutionCTupstream_gene_variant
MELA-AU101588127815881278single base substitutionCTintron_variant
MELA-AU101588127815881278single base substitutionCTupstream_gene_variant
MELA-AU101588144615881446single base substitutionACintron_variant
MELA-AU101588144615881446single base substitutionACupstream_gene_variant
MELA-AU101588147515881475single base substitutionGAintron_variant
MELA-AU101588147515881475single base substitutionGAupstream_gene_variant
MELA-AU101588237915882380deletion of <=200bpTG-intron_variant
MELA-AU101588237915882380deletion of <=200bpTG-upstream_gene_variant
MELA-AU101588285115882851single base substitutionGAintron_variant
MELA-AU101588285115882851single base substitutionGAupstream_gene_variant
MELA-AU101588467815884678single base substitutionGTintron_variant
MELA-AU101588467815884678single base substitutionGTupstream_gene_variant
MELA-AU101588500215885002single base substitutionCTintron_variant
MELA-AU101588500215885002single base substitutionCTupstream_gene_variant
MELA-AU101588506015885060single base substitutionGAintron_variant
MELA-AU101588506015885060single base substitutionGAupstream_gene_variant
MELA-AU101588534915885349single base substitutionACintron_variant
MELA-AU101588536215885362single base substitutionAGintron_variant
MELA-AU101588552815885528single base substitutionGAintron_variant
MELA-AU101588588915885889single base substitutionGAintron_variant
MELA-AU101588603915886039single base substitutionGAintron_variant
MELA-AU101588611315886113single base substitutionAGintron_variant
MELA-AU101588649415886494single base substitutionAGintron_variant
MELA-AU101588667915886679single base substitutionACintron_variant
MELA-AU101588710915887109single base substitutionACintron_variant
MELA-AU101588718015887180single base substitutionCTintron_variant
MELA-AU101588724315887243single base substitutionGAintron_variant
MELA-AU101588758915887589single base substitutionCTintron_variant
MELA-AU101588782115887821single base substitutionTAintron_variant
MELA-AU101589023715890237single base substitutionGAintron_variant
MELA-AU101589108015891080single base substitutionGAintron_variant
MELA-AU101589149015891490single base substitutionGAintron_variant
MELA-AU101589169615891696single base substitutionGAintron_variant
MELA-AU101589226815892268single base substitutionTCintron_variant
MELA-AU101589309115893091single base substitutionTCintron_variant
MELA-AU101589345815893458single base substitutionCTintron_variant
MELA-AU101589356915893569single base substitutionCAintron_variant
MELA-AU101589458215894582single base substitutionATintron_variant
MELA-AU101589516315895163single base substitutionTAintron_variant
MELA-AU101589520015895200single base substitutionGAintron_variant
MELA-AU101589661515896615single base substitutionTCintron_variant
MELA-AU101589704415897044single base substitutionGAintron_variant
MELA-AU101589706115897061single base substitutionATintron_variant
MELA-AU101589716715897167single base substitutionATintron_variant
MELA-AU101589741215897412single base substitutionCTintron_variant
MELA-AU101589760815897611deletion of <=200bpATGA-intron_variant
MELA-AU101589795715897957single base substitutionGAintron_variant
MELA-AU101589800015898000single base substitutionATintron_variant
MELA-AU101589850615898506single base substitutionGAintron_variant
MELA-AU101589866615898666single base substitutionACintron_variant
MELA-AU101590070915900709single base substitutionTCintron_variant
MELA-AU101590235415902354single base substitutionGA5_prime_UTR_variant
MELA-AU101590235415902354single base substitutionGAexon_variant
MELA-AU101590256115902561single base substitutionGAupstream_gene_variant
MELA-AU101590256215902562single base substitutionGAupstream_gene_variant
MELA-AU101590256715902567single base substitutionCTupstream_gene_variant
MELA-AU101590369315903693single base substitutionCTupstream_gene_variant
MELA-AU101590405115904051single base substitutionCTupstream_gene_variant
MELA-AU101590509015905090single base substitutionTCupstream_gene_variant
MELA-AU101590586615905867multiple base substitution (>=2bp and <=200bp)TCAGupstream_gene_variant
MELA-AU101590599215905992single base substitutionCTupstream_gene_variant
MELA-AU101590619915906199single base substitutionCTupstream_gene_variant
MELA-AU101590628315906283single base substitutionCTupstream_gene_variant
MELA-AU101590692715906927single base substitutionTAupstream_gene_variant
MELA-AU101590705015907050single base substitutionTCupstream_gene_variant
MELA-AU101590712315907123single base substitutionGAupstream_gene_variant
MELA-AU101590741515907415single base substitutionCTupstream_gene_variant
ORCA-IN101584386515843865single base substitutionCTintron_variant
ORCA-IN101588073015880730single base substitutionCTintron_variant
ORCA-IN101588073015880730single base substitutionCTupstream_gene_variant
ORCA-IN101589751015897510single base substitutionGAintron_variant
OV-AU101582058715820587single base substitutionTA3_prime_UTR_variant
OV-AU101582058715820587single base substitutionTAdownstream_gene_variant
OV-AU101582058715820587single base substitutionTAexon_variant
OV-AU101582346815823468single base substitutionTCintron_variant
OV-AU101582877915828779single base substitutionTGdownstream_gene_variant
OV-AU101582877915828779single base substitutionTGintron_variant
OV-AU101582877915828779single base substitutionTGupstream_gene_variant
OV-AU101583016015830160single base substitutionGCdownstream_gene_variant
OV-AU101583016015830160single base substitutionGCintron_variant
OV-AU101583289515832895single base substitutionGTintron_variant
OV-AU101583539115835391single base substitutionTCdownstream_gene_variant
OV-AU101583539115835391single base substitutionTCintron_variant
OV-AU101584369515843695single base substitutionCAintron_variant
OV-AU101584926215849262single base substitutionGAintron_variant
OV-AU101585248015852480single base substitutionGAintron_variant
OV-AU101585446215854462single base substitutionGTintron_variant
OV-AU101586109815861098single base substitutionATintron_variant
OV-AU101586109815861098single base substitutionATupstream_gene_variant
OV-AU101587114715871147single base substitutionCAintron_variant
OV-AU101587296515872965single base substitutionCGintron_variant
OV-AU101587367715873677single base substitutionTCintron_variant
OV-AU101587443615874436single base substitutionCGintron_variant
OV-AU101587795715877957single base substitutionCTintron_variant
OV-AU101587933815879338single base substitutionACintron_variant
OV-AU101587933815879338single base substitutionACupstream_gene_variant
OV-AU101588190615881906single base substitutionGAintron_variant
OV-AU101588190615881906single base substitutionGAupstream_gene_variant
OV-AU101588609615886096single base substitutionCGintron_variant
OV-AU101589968315899683single base substitutionAGintron_variant
OV-AU101590535115905351single base substitutionGAupstream_gene_variant
PACA-AU101581943815819438single base substitutionCAdownstream_gene_variant
PACA-AU101582777615827776single base substitutionTCdownstream_gene_variant
PACA-AU101582777615827776single base substitutionTCintron_variant
PACA-AU101582777615827776single base substitutionTCupstream_gene_variant
PACA-AU101582957615829576single base substitutionGTdownstream_gene_variant
PACA-AU101582957615829576single base substitutionGTintron_variant
PACA-AU101583132815831328insertion of <=200bp-Aintron_variant
PACA-AU101583155415831554single base substitutionGAintron_variant
PACA-AU101583502815835028single base substitutionGAdownstream_gene_variant
PACA-AU101583502815835028single base substitutionGAintron_variant
PACA-AU101585667615856676single base substitutionGTintron_variant
PACA-AU101585855315858553single base substitutionTCintron_variant
PACA-AU101585963415859634single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
PACA-AU101585963415859634single base substitutionGAintron_variant
PACA-AU101586373415863736deletion of <=200bpAAC-intron_variant
PACA-AU101586373415863736deletion of <=200bpAAC-upstream_gene_variant
PACA-AU101586477315864773single base substitutionGCintron_variant
PACA-AU101586477315864773single base substitutionGCupstream_gene_variant
PACA-AU101586492315864923deletion of <=200bpA-intron_variant
PACA-AU101586492315864923deletion of <=200bpA-upstream_gene_variant
PACA-AU101586662415866624single base substitutionTCintron_variant
PACA-AU101586759915867599single base substitutionGTintron_variant
PACA-AU101586761515867615single base substitutionCGintron_variant
PACA-AU101587105215871052single base substitutionCTintron_variant
PACA-AU101587596115875961single base substitutionGTintron_variant
PACA-AU101587673715876737single base substitutionGAintron_variant
PACA-AU101588030315880303single base substitutionCAintron_variant
PACA-AU101588030315880303single base substitutionCAupstream_gene_variant
PACA-AU101588170215881702single base substitutionCAintron_variant
PACA-AU101588170215881702single base substitutionCAupstream_gene_variant
PACA-AU101589524915895249deletion of <=200bpA-intron_variant
PACA-AU101589779115897791deletion of <=200bpA-intron_variant
PACA-CA101582400315824003single base substitutionAGintron_variant
PACA-CA101582744215827442single base substitutionGAdownstream_gene_variant
PACA-CA101582744215827442single base substitutionGAintron_variant
PACA-CA101582744215827442single base substitutionGAupstream_gene_variant
PACA-CA101582792515827925single base substitutionTCdownstream_gene_variant
PACA-CA101582792515827925single base substitutionTCintron_variant
PACA-CA101582792515827925single base substitutionTCupstream_gene_variant
PACA-CA101583132815831328deletion of <=200bpA-intron_variant
PACA-CA101583290915832909single base substitutionCTintron_variant
PACA-CA101583547515835475single base substitutionGAdownstream_gene_variant
PACA-CA101583547515835475single base substitutionGAintron_variant
PACA-CA101583565115835651single base substitutionAGdownstream_gene_variant
PACA-CA101583565115835651single base substitutionAGintron_variant
PACA-CA101583566915835669single base substitutionGTdownstream_gene_variant
PACA-CA101583566915835669single base substitutionGTintron_variant
PACA-CA101583757815837578single base substitutionCGdownstream_gene_variant
PACA-CA101583757815837578single base substitutionCGintron_variant
PACA-CA101584117815841178deletion of <=200bpT-intron_variant
PACA-CA101584168215841682single base substitutionGAintron_variant
PACA-CA101584176415841764single base substitutionGAintron_variant
PACA-CA101584313215843132single base substitutionCTintron_variant
PACA-CA101584611515846128deletion of <=200bpATTTTATCAGAGGA-intron_variant
PACA-CA101584915015849150single base substitutionACintron_variant
PACA-CA101585189715851897single base substitutionGTintron_variant
PACA-CA101585244515852445single base substitutionCTintron_variant
PACA-CA101585944615859449deletion of <=200bpTTCA-5_prime_UTR_variant
PACA-CA101585944615859449deletion of <=200bpTTCA-intron_variant
PACA-CA101585945315859453insertion of <=200bp-G5_prime_UTR_variant
PACA-CA101585945315859453insertion of <=200bp-Gintron_variant
PACA-CA101586032915860329single base substitutionCAintron_variant
PACA-CA101586032915860329single base substitutionCAupstream_gene_variant
PACA-CA101586751515867515single base substitutionGAintron_variant
PACA-CA101586979315869793single base substitutionGAintron_variant
PACA-CA101587327015873270single base substitutionACintron_variant
PACA-CA101587555615875556single base substitutionCTintron_variant
PACA-CA101587612815876128single base substitutionTCintron_variant
PACA-CA101587613615876136single base substitutionATintron_variant
PACA-CA101587849815878498insertion of <=200bp-Aintron_variant
PACA-CA101587932515879325deletion of <=200bpA-splice_region_variant
PACA-CA101587932515879325deletion of <=200bpA-upstream_gene_variant
PACA-CA101587988815879888deletion of <=200bpA-intron_variant
PACA-CA101587988815879888deletion of <=200bpA-upstream_gene_variant
PACA-CA101588529715885297single base substitutionGCintron_variant
PACA-CA101588610815886108single base substitutionGCintron_variant
PACA-CA101588700115887001single base substitutionCGintron_variant
PACA-CA101589159015891590deletion of <=200bpA-intron_variant
PACA-CA101589462515894625single base substitutionGTintron_variant
PACA-CA101589915515899155single base substitutionTCintron_variant
PACA-CA101590273215902732single base substitutionGAupstream_gene_variant
PACA-CA101590663115906631single base substitutionCAupstream_gene_variant
PACA-CA101590678015906780single base substitutionTGupstream_gene_variant
PAEN-AU101581557515815575single base substitutionAGdownstream_gene_variant
PAEN-AU101585277715852777single base substitutionTAintron_variant
PAEN-AU101585799015857990single base substitutionCGintron_variant
PAEN-AU101587893015878930single base substitutionCTintron_variant
PAEN-IT101583576615835766single base substitutionCAdownstream_gene_variant
PAEN-IT101583576615835766single base substitutionCAintron_variant
PAEN-IT101585156015851560single base substitutionCTintron_variant
PAEN-IT101589684115896841single base substitutionGTintron_variant
PAEN-IT101590080615900806single base substitutionTGintron_variant
PBCA-DE101581932815819328single base substitutionCGdownstream_gene_variant
PBCA-DE101582265315822653single base substitutionCGintron_variant
PBCA-DE101584297915842979single base substitutionGTintron_variant
PBCA-DE101585608315856083single base substitutionATintron_variant
PBCA-DE101586031715860317deletion of <=200bpA-intron_variant
PBCA-DE101586031715860317deletion of <=200bpA-upstream_gene_variant
PBCA-DE101586387315863873insertion of <=200bp-TATTTATTAGGAGATAATGTCAACintron_variant
PBCA-DE101586387315863873insertion of <=200bp-TATTTATTAGGAGATAATGTCAACupstream_gene_variant
PBCA-DE101588364015883640deletion of <=200bpA-intron_variant
PBCA-DE101588364015883640deletion of <=200bpA-upstream_gene_variant
PBCA-DE101588855115888551insertion of <=200bp-Aintron_variant
PBCA-DE101589195115891951single base substitutionGTintron_variant
PRAD-CA101587135015871350single base substitutionTGintron_variant
PRAD-CA101588130115881301single base substitutionGAintron_variant
PRAD-CA101588130115881301single base substitutionGAupstream_gene_variant
PRAD-CA101589926515899265single base substitutionGCintron_variant
PRAD-CA101590415515904155single base substitutionAGupstream_gene_variant
PRAD-CA101590575815905758single base substitutionGAupstream_gene_variant
PRAD-CA101590592615905926single base substitutionATupstream_gene_variant
PRAD-UK101582013715820137single base substitutionTCdownstream_gene_variant
PRAD-UK101582229915822299single base substitutionAGintron_variant
PRAD-UK101582636815826368single base substitutionAGdownstream_gene_variant
PRAD-UK101582636815826368single base substitutionAGintron_variant
PRAD-UK101582636815826368single base substitutionAGupstream_gene_variant
PRAD-UK101584827515848275single base substitutionGAintron_variant
PRAD-UK101588108415881084single base substitutionAGintron_variant
PRAD-UK101588108415881084single base substitutionAGupstream_gene_variant
PRAD-UK101588981415889814single base substitutionACintron_variant
PRAD-UK101590485015904850single base substitutionGAupstream_gene_variant
PRAD-UK101590601315906013single base substitutionTGupstream_gene_variant
READ-US101587659415876594single base substitutionCTexon_variant
READ-US101587659415876594single base substitutionCTmissense_variantE200K598G>A
READ-US101587659415876594single base substitutionCTmissense_variantE40K118G>A
READ-US101587659415876594single base substitutionCTmissense_variantE53K157G>A
RECA-EU101584170415841704single base substitutionATintron_variant
RECA-EU101584982315849823single base substitutionAGintron_variant
RECA-EU101585200715852007single base substitutionAGintron_variant
RECA-EU101585202915852029single base substitutionAGintron_variant
RECA-EU101587031115870311single base substitutionTAintron_variant
RECA-EU101587558915875589single base substitutionTCintron_variant
RECA-EU101587833315878333single base substitutionTAintron_variant
RECA-EU101588191115881911single base substitutionTAintron_variant
RECA-EU101588191115881911single base substitutionTAupstream_gene_variant
RECA-EU101589109615891096single base substitutionTAintron_variant
SKCA-BR101581559915815599single base substitutionCTdownstream_gene_variant
SKCA-BR101581692915816929single base substitutionTCdownstream_gene_variant
SKCA-BR101581693215816932single base substitutionATdownstream_gene_variant
SKCA-BR101581891815818918single base substitutionGAdownstream_gene_variant
SKCA-BR101581976315819763single base substitutionGAdownstream_gene_variant
SKCA-BR101581985415819854single base substitutionGAdownstream_gene_variant
SKCA-BR101582032215820322single base substitutionAG3_prime_UTR_variant
SKCA-BR101582032215820322single base substitutionAGdownstream_gene_variant
SKCA-BR101582032215820322single base substitutionAGexon_variant
SKCA-BR101582184815821848single base substitutionTGintron_variant
SKCA-BR101582684015826840single base substitutionGAdownstream_gene_variant
SKCA-BR101582684015826840single base substitutionGAintron_variant
SKCA-BR101582684015826840single base substitutionGAupstream_gene_variant
SKCA-BR101582685015826850single base substitutionGAdownstream_gene_variant
SKCA-BR101582685015826850single base substitutionGAintron_variant
SKCA-BR101582685015826850single base substitutionGAupstream_gene_variant
SKCA-BR101583078815830788single base substitutionGAdownstream_gene_variant
SKCA-BR101583078815830788single base substitutionGAintron_variant
SKCA-BR101583931115839311single base substitutionAGintron_variant
SKCA-BR101584004915840049single base substitutionGAintron_variant
SKCA-BR101584046315840463insertion of <=200bp-GTTintron_variant
SKCA-BR101584193815841938single base substitutionAGintron_variant
SKCA-BR101584328415843284single base substitutionGAintron_variant
SKCA-BR101584674715846747single base substitutionGAintron_variant
SKCA-BR101585415915854159single base substitutionCTintron_variant
SKCA-BR101585828715858287single base substitutionGAintron_variant
SKCA-BR101586579015865790single base substitutionCTintron_variant
SKCA-BR101586828915868289single base substitutionTAintron_variant
SKCA-BR101586930215869302single base substitutionAGintron_variant
SKCA-BR101587471815874718single base substitutionTAintron_variant
SKCA-BR101587650215876502single base substitutionTGintron_variant
SKCA-BR101587723115877231single base substitutionAGintron_variant
SKCA-BR101588622715886227single base substitutionCTintron_variant
SKCA-BR101588673315886733single base substitutionTCintron_variant
SKCA-BR101589066115890662deletion of <=200bpAG-intron_variant
SKCA-BR101589724215897242single base substitutionGAintron_variant
SKCA-BR101590054515900545single base substitutionGAintron_variant
SKCA-BR101590393515903935single base substitutionCTupstream_gene_variant
SKCA-BR101590538415905384single base substitutionCTupstream_gene_variant
SKCA-BR101590708115907081single base substitutionCTupstream_gene_variant
SKCM-US101582420615824206single base substitutionGAexon_variant
SKCM-US101582420615824206single base substitutionGAmissense_variantS379F1136C>T
SKCM-US101582420615824206single base substitutionGAmissense_variantS84F251C>T
SKCM-US101582860215828602single base substitutionGAdownstream_gene_variant
SKCM-US101582860215828602single base substitutionGAexon_variant
SKCM-US101582860215828602single base substitutionGAsynonymous_variantI358I1074C>T
SKCM-US101582860215828602single base substitutionGAsynonymous_variantI63I189C>T
SKCM-US101582860215828602single base substitutionGAupstream_gene_variant
SKCM-US101582864015828640single base substitutionGAdownstream_gene_variant
SKCM-US101582864015828640single base substitutionGAexon_variant
SKCM-US101582864015828640single base substitutionGAmissense_variantL346F1036C>T
SKCM-US101582864015828640single base substitutionGAmissense_variantL51F151C>T
SKCM-US101582864015828640single base substitutionGAupstream_gene_variant
SKCM-US101583811015838110single base substitutionTAdownstream_gene_variant
SKCM-US101583811015838110single base substitutionTAexon_variant
SKCM-US101583811015838110single base substitutionTAmissense_variantY155F464A>T
SKCM-US101583811015838110single base substitutionTAmissense_variantY20F59A>T
SKCM-US101583811015838110single base substitutionTAmissense_variantY315F944A>T
SKCM-US101585888515858885single base substitutionGA5_prime_UTR_variant
SKCM-US101585888515858885single base substitutionGAexon_variant
SKCM-US101585888515858885single base substitutionGAsynonymous_variantF117F351C>T
SKCM-US101585888515858885single base substitutionGAsynonymous_variantF130F390C>T
SKCM-US101585888515858885single base substitutionGAsynonymous_variantF277F831C>T
SKCM-US101587930915879309single base substitutionGAexon_variant
SKCM-US101587930915879309single base substitutionGAmissense_variantS10L29C>T
SKCM-US101587930915879309single base substitutionGAmissense_variantS157L470C>T
SKCM-US101587930915879309single base substitutionGAupstream_gene_variant
SKCM-US101588524015885240single base substitutionGAexon_variant
SKCM-US101588524015885240single base substitutionGAmissense_variantS69L206C>T
SKCM-US101588524015885240single base substitutionGAupstream_gene_variant
STAD-US101582113315821133single base substitutionTCexon_variant
STAD-US101582113315821133single base substitutionTCmissense_variantY104C311A>G
STAD-US101582113315821133single base substitutionTCmissense_variantY399C1196A>G
STAD-US101583815515838155single base substitutionGAexon_variant
STAD-US101583815515838155single base substitutionGAmissense_variantA140V419C>T
STAD-US101583815515838155single base substitutionGAmissense_variantA153V458C>T
STAD-US101583815515838155single base substitutionGAmissense_variantA300V899C>T
STAD-US101583815515838155single base substitutionGAmissense_variantA5V14C>T
STAD-US101587566015875660single base substitutionTCexon_variant
STAD-US101587566015875660single base substitutionTCsynonymous_variantV233V699A>G
STAD-US101587566015875660single base substitutionTCsynonymous_variantV73V219A>G
STAD-US101587566015875660single base substitutionTCsynonymous_variantV86V258A>G
STAD-US101587925915879259single base substitutionTCexon_variant
STAD-US101587925915879259single base substitutionTCmissense_variantM14V40A>G
STAD-US101587925915879259single base substitutionTCmissense_variantM174V520A>G
STAD-US101587925915879259single base substitutionTCmissense_variantM27V79A>G
STAD-US101588345915883459single base substitutionAGexon_variant
STAD-US101588345915883459single base substitutionAGsynonymous_variantS125S375T>C
STAD-US101588345915883459single base substitutionAGupstream_gene_variant
STAD-US101588523915885239single base substitutionCTexon_variant
STAD-US101588523915885239single base substitutionCTsynonymous_variantS69S207G>A
STAD-US101588523915885239single base substitutionCTupstream_gene_variant
THCA-SA101590221015902210single base substitutionGTexon_variant
THCA-SA101590221015902210single base substitutionGTmissense_variantT30K89C>A
UCEC-US101582099615820996single base substitutionTGexon_variant
UCEC-US101582099615820996single base substitutionTGmissense_variantN150H448A>C
UCEC-US101582099615820996single base substitutionTGmissense_variantN445H1333A>C
UCEC-US101582113215821132single base substitutionGAexon_variant
UCEC-US101582113215821132single base substitutionGAsynonymous_variantY104Y312C>T
UCEC-US101582113215821132single base substitutionGAsynonymous_variantY399Y1197C>T
UCEC-US101582860715828607single base substitutionCGdownstream_gene_variant
UCEC-US101582860715828607single base substitutionCGexon_variant
UCEC-US101582860715828607single base substitutionCGmissense_variantG357R1069G>C
UCEC-US101582860715828607single base substitutionCGmissense_variantG62R184G>C
UCEC-US101582860715828607single base substitutionCGupstream_gene_variant
UCEC-US101583810715838107single base substitutionTCdownstream_gene_variant
UCEC-US101583810715838107single base substitutionTCexon_variant
UCEC-US101583810715838107single base substitutionTCmissense_variantD156G467A>G
UCEC-US101583810715838107single base substitutionTCmissense_variantD21G62A>G
UCEC-US101583810715838107single base substitutionTCmissense_variantD316G947A>G
UCEC-US101583811915838119single base substitutionACexon_variant
UCEC-US101583811915838119single base substitutionACmissense_variantF152C455T>G
UCEC-US101583811915838119single base substitutionACmissense_variantF17C50T>G
UCEC-US101583811915838119single base substitutionACmissense_variantF312C935T>G
UCEC-US101583811915838119single base substitutionACsynonymous_variant?165
UCEC-US101587568215875682single base substitutionGAexon_variant
UCEC-US101587568215875682single base substitutionGAmissense_variantT226M677C>T
UCEC-US101587568215875682single base substitutionGAmissense_variantT66M197C>T
UCEC-US101587568215875682single base substitutionGAmissense_variantT79M236C>T
UCEC-US101587930915879309single base substitutionGAexon_variant
UCEC-US101587930915879309single base substitutionGAmissense_variantS10L29C>T
UCEC-US101587930915879309single base substitutionGAmissense_variantS157L470C>T
UCEC-US101587930915879309single base substitutionGAupstream_gene_variant
UCEC-US101588352115883521single base substitutionAGexon_variant
UCEC-US101588352115883521single base substitutionAGmissense_variantY105H313T>C
UCEC-US101588352115883521single base substitutionAGupstream_gene_variant
UCEC-US101588354315883543single base substitutionAGexon_variant
UCEC-US101588354315883543single base substitutionAGsynonymous_variantA97A291T>C
UCEC-US101588354315883543single base substitutionAGupstream_gene_variant
UCEC-US101588522315885223single base substitutionGAexon_variant
UCEC-US101588522315885223single base substitutionGAmissense_variantR75W223C>T
UCEC-US101588522315885223single base substitutionGAupstream_gene_variant
UCEC-US101588524015885240single base substitutionGAexon_variant
UCEC-US101588524015885240single base substitutionGAmissense_variantS69L206C>T
UCEC-US101588524015885240single base substitutionGAupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
041TCOSM1728925c.920A>Tp.Q307LSubstitution - Missense10:15796135-15796135-
TCGA-EE-A2MR-06COSM916749c.206C>Tp.S69LSubstitution - Missense10:15843241-15843241-
pfg008TCOSM1638501c.850A>Gp.S284GSubstitution - Missense10:15816867-15816867-
TCGA-BR-8680-01COSM4013050c.1196A>Gp.Y399CSubstitution - Missense10:15779134-15779134-
ME043TCOSM228522c.1021C>Tp.P341SSubstitution - Missense10:15789254-15789254-
TCGA-BS-A0UF-01COSM916739c.1333A>Cp.N445HSubstitution - Missense10:15778997-15778997-
TCGA-EP-A2KB-01COSM4921494c.402A>Gp.E134ESubstitution - coding silent10:15841433-15841433-
GHE0624COSM5714310c.731-3C>Tp.?Unknown10:15821729-15821729-
TCGA-BR-6452-01COSM4013057c.375T>Cp.S125SSubstitution - coding silent10:15841460-15841460-
ESCC_BICR_034TCOSM5443573c.680delGp.G227fs*17Deletion - Frameshift10:15833680-15833680-
TCGA-CD-A4MH-01COSM4013055c.520A>Gp.M174VSubstitution - Missense10:15837260-15837260-
TCGA-13-0793-01COSM82034c.624G>Ap.L208LSubstitution - coding silent10:15834569-15834569-
J33_TCOSM3978319c.671T>Ap.L224QSubstitution - Missense10:15833689-15833689-
TCGA-G4-6302-01COSM3686666c.1180A>Gp.N394DSubstitution - Missense10:15782163-15782163-
TCGA-FW-A3R5-06COSM3866944c.1036C>Tp.L346FSubstitution - Missense10:15786641-15786641-
TCGA-ED-A4XI-01COSM4913169c.580A>Gp.I194VSubstitution - Missense10:15834613-15834613-
TCGA-56-6545-01COSM683799c.445T>Cp.F149LSubstitution - Missense10:15838244-15838244-
TCGA-GM-A3NW-01COSM3806851c.474C>Gp.F158LSubstitution - Missense10:15837306-15837306-
TCGA-AA-3952-01COSM296988c.780G>Ap.M260ISubstitution - Missense10:15821677-15821677-
TCGA-AZ-4315-01COSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
T3021COSM4682806c.222G>Ap.W74*Substitution - Nonsense10:15843225-15843225-
pfg054TCOSM4750364c.71C>Tp.T24ISubstitution - Missense10:15860229-15860229-
384COSM4426732c.681A>Gp.G227GSubstitution - coding silent10:15833679-15833679-
TCGA-BR-4201-01COSM4013058c.207G>Ap.S69SSubstitution - coding silent10:15843240-15843240-
HCT15COSM2131472c.643C>Gp.H215DSubstitution - Missense10:15834550-15834550-
HCC25COSM1603266c.825A>Gp.P275PSubstitution - coding silent10:15816892-15816892-
cSCCP1COSM135969c.1328C>Tp.S443LSubstitution - Missense10:15779002-15779002-
XHDG40COSM4770073c.812A>Tp.Y271FSubstitution - Missense10:15816905-15816905-
T1154COSM4682803c.944A>Gp.Y315CSubstitution - Missense10:15796111-15796111-
PT36COSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
381_TCOSM3978322c.163G>Ap.A55TSubstitution - Missense10:15847875-15847875-
TCGA-BP-5174-01COSM465495c.536T>Cp.F179SSubstitution - Missense10:15837244-15837244-
TCGA-FS-A4F0-06COSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
CSCC-31-TCOSM4472985c.181C>Tp.L61FSubstitution - Missense10:15843266-15843266-
DU-145COSM1675071c.1308G>Tp.W436CSubstitution - Missense10:15779022-15779022-
TCGA-B2-5635-01COSM465494c.678G>Ap.T226TSubstitution - coding silent10:15833682-15833682-
TCGA-CM-6172-01COSM5160409c.956-7C>Ap.?Unknown10:15789326-15789326-
46MCOSM5587768c.631C>Tp.P211SSubstitution - Missense10:15834562-15834562-
pfg008TCOSM1638501c.850A>Gp.S284GSubstitution - Missense10:15816867-15816867-
TCGA-AA-A010-01COSM299209c.1136C>Ap.S379YSubstitution - Missense10:15782207-15782207-
3N26-VS-3T26COSM4980064c.1228G>Cp.E410QSubstitution - Missense10:15779102-15779102-
TCGA-A8-A095-01COSM427343c.1041G>Ap.M347ISubstitution - Missense10:15786636-15786636-
Pat_04_ACOSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
HCT15COSM2131489c.204T>Ap.S68SSubstitution - coding silent10:15843243-15843243-
TCGA-BS-A0UF-01COSM916740c.1197C>Tp.Y399YSubstitution - coding silent10:15779133-15779133-
TCGA-A2-A0SY-01COSM427344c.840G>Ap.W280*Substitution - Nonsense10:15816877-15816877-
B35-TumorCOSM1745725c.926G>Ap.R309KSubstitution - Missense10:15796129-15796129-
TCGA-BP-4165-01COSM3358696c.426A>Tp.E142DSubstitution - Missense10:15838263-15838263-
587346COSM1206240c.392G>Tp.C131FSubstitution - Missense10:15841443-15841443-
TCGA-D8-A1XK-01COSM3806850c.940A>Gp.T314ASubstitution - Missense10:15796115-15796115-
PTC_117COSM5957601c.89C>Ap.T30KSubstitution - Missense10:15860211-15860211-
SNU-C2BCOSM2131474c.622T>Cp.L208LSubstitution - coding silent10:15834571-15834571-
TCGA-EE-A3AD-06COSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
CHC1028TCOSM4790838c.908C>Tp.A303VSubstitution - Missense10:15796147-15796147-
TCGA-AX-A060-01COSM916742c.947A>Gp.D316GSubstitution - Missense10:15796108-15796108-
T3225COSM4682805c.234A>Gp.S78SSubstitution - coding silent10:15843213-15843213-
CCK81COSM2131456c.1276C>Tp.Q426*Substitution - Nonsense10:15779054-15779054-
TCGA-A5-A0GH-01COSM916746c.313T>Cp.Y105HSubstitution - Missense10:15841522-15841522-
TCGA-EI-6917-01COSM3414876c.598G>Ap.E200KSubstitution - Missense10:15834595-15834595-
B35COSM1745725c.926G>Ap.R309KSubstitution - Missense10:15796129-15796129-
TCGA-BS-A0UL-01COSM916748c.223C>Tp.R75WSubstitution - Missense10:15843224-15843224-
TCGA-D1-A17F-01COSM916744c.677C>Tp.T226MSubstitution - Missense10:15833683-15833683-
PT08_2COSM5893464c.956-7C>Tp.?Unknown10:15789326-15789326-
TCGA-BS-A0UF-01COSM916743c.935T>Gp.F312CSubstitution - Missense10:15796120-15796120-
TCGA-EE-A3J5-06COSM3436253c.831C>Tp.F277FSubstitution - coding silent10:15816886-15816886-
61COSM5738838c.754G>Tp.A252SSubstitution - Missense10:15821703-15821703-
TCGA-BR-4184-01COSM4013051c.899C>Tp.A300VSubstitution - Missense10:15796156-15796156-
T3024COSM4682802c.1069G>Ap.G357RSubstitution - Missense10:15786608-15786608-
TCGA-BC-A10U-01COSM4942490c.882+2T>Cp.?Unknown10:15816833-15816833-
TCGA-DA-A1HV-06COSM3436250c.1136C>Tp.S379FSubstitution - Missense10:15782207-15782207-
TCGA-AX-A0J0-01COSM916747c.291T>Cp.A97ASubstitution - coding silent10:15841544-15841544-
CCK81COSM2131466c.876delTp.F292fs*7Deletion - Frameshift10:15816841-15816841-
J85_TCOSM3978321c.422T>Cp.V141ASubstitution - Missense10:15838267-15838267-
LUAD-S01306COSM343396c.309A>Gp.G103GSubstitution - coding silent10:15841526-15841526-
HCC25TCOSM1603266c.825A>Gp.P275PSubstitution - coding silent10:15816892-15816892-
TCGA-BR-4361-01COSM4013053c.699A>Gp.V233VSubstitution - coding silent10:15833661-15833661-
DLD1COSM2131489c.204T>Ap.S68SSubstitution - coding silent10:15843243-15843243-
2492720COSM5721465c.1318C>Tp.R440CSubstitution - Missense10:15779012-15779012-
CSCC-30-TCOSM4526949c.142G>Ap.G48SSubstitution - Missense10:15847896-15847896-
CHC1028TCOSM4790838c.908C>Tp.A303VSubstitution - Missense10:15796147-15796147-
TCGA-G4-6309-01COSM1347079c.902_903insCp.E302fs*1Insertion - Frameshift10:15796152-15796153-
ESCC_60COSM5632672c.964T>Cp.F322LSubstitution - Missense10:15789311-15789311-
CSCC-16-TCOSM4545164c.371G>Ap.G124ESubstitution - Missense10:15841464-15841464-
TCGA-EE-A2GI-06COSM3436251c.1074C>Tp.I358ISubstitution - coding silent10:15786603-15786603-
SA090COSM213562c.119G>Tp.G40VSubstitution - Missense10:15847919-15847919-
TCGA-CJ-4895-01COSM3358697c.74T>Cp.I25TSubstitution - Missense10:15860226-15860226-
TCGA-BS-A0U5-01COSM916741c.1069G>Cp.G357RSubstitution - Missense10:15786608-15786608-
TCGA-85-6560-01COSM683798c.225G>Tp.R75RSubstitution - coding silent10:15843222-15843222-
TCGA-CF-A3MI-01COSM1297140c.731-1G>Ap.?Unknown10:15821727-15821727-
HX10TCOSM1603268c.111A>Gp.E37ESubstitution - coding silent10:15847927-15847927-
TCGA-23-2645-01COSM1321439c.946G>Ap.D316NSubstitution - Missense10:15796109-15796109-
LP6005334-DNA_E01COSM5034578c.1116+9G>Cp.?Unknown10:15786552-15786552-
BD236TCOSM5518062c.956-10delTp.?Unknown10:15789329-15789329-
TCGA-A5-A0GP-01COSM916745c.470C>Tp.S157LSubstitution - Missense10:15837310-15837310-
TCGA-GV-A3QI-01COSM1297141c.728T>Cp.M243TSubstitution - Missense10:15833632-15833632-
PT08_1COSM5893464c.956-7C>Tp.?Unknown10:15789326-15789326-
TCGA-EE-A29L-06COSM3436252c.944A>Tp.Y315FSubstitution - Missense10:15796111-15796111-
CSCC-32-TCOSM4572804c.871T>Ap.F291ISubstitution - Missense10:15816846-15816846-
CSCC-49-TCOSM4546506c.400G>Ap.E134KSubstitution - Missense10:15841435-15841435-
CSCC-41-TCOSM3436250c.1136C>Tp.S379FSubstitution - Missense10:15782207-15782207-
2492722COSM5721465c.1318C>Tp.R440CSubstitution - Missense10:15779012-15779012-
LUAD-NYU1051SCOSM368466c.308G>Tp.G103VSubstitution - Missense10:15841527-15841527-
2492721COSM5721465c.1318C>Tp.R440CSubstitution - Missense10:15779012-15779012-
T3024COSM4682804c.308G>Ap.G103ESubstitution - Missense10:15841527-15841527-
2492723COSM5721465c.1318C>Tp.R440CSubstitution - Missense10:15779012-15779012-
PT48COSM5932611c.949C>Tp.P317SSubstitution - Missense10:15796106-15796106-
40MCOSM3414876c.598G>Ap.E200KSubstitution - Missense10:15834595-15834595-
TCGA-BS-A0UF-01COSM916749c.206C>Tp.S69LSubstitution - Missense10:15843241-15843241-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.158769;Hs.158778;Hs.158785;Hs.158786;Hs.158797;Hs.158826;Hs.158830;Hs.158845;Hs.158851;Hs.158852;Hs.158853;Hs.158859;Hs.158863;Hs.15887010p13611649
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.F149Lc.445T>C1015880243LUSC
AGMissensep.F179Sc.536T>C1015879243RCCC
AGMissensep.I25Tc.74T>C1015902225RCCC
AGMissensep.M243Tc.728T>C1015875631BLCA
AGMissensep.Y105Hc.313T>C1015883521UCEC
CAMissensep.D295Yc.883G>T1015838171HNSC
CAMissensep.G362Cc.1084G>T1015828592HNSC
CAMissensep.G40Vc.119G>T1015889918BRCA
CASpliceAcceptorSNV.c.236-1G>T1015883599LUAD
CASynonymousp.R75Rc.225G>T1015885221LUSC
CGMissensep.G357Rc.1069G>C1015828607UCEC
CTMissensep.E367Kc.1099G>A1015828577CM
CTMissensep.M260Ic.780G>A1015863676COREAD
CTMissensep.M347Ic.1041G>A1015828635BRCA
CTNonsensep.W280*c.840G>A1015858876BRCA
CTSpliceAcceptorSNV.c.731-1G>A1015863726BLCA
CTSynonymousp.L208Lc.624G>A1015876568OV
CTSynonymousp.S69Sc.207G>A1015885239STAD
GAMissensep.P341Sc.1021C>T1015831253CM
GAMissensep.R75Wc.223C>T1015885223UCEC
GAMissensep.S157Lc.470C>T1015879309CM
GAMissensep.S157Lc.470C>T1015879309UCEC
GAMissensep.S379Fc.1136C>T1015824206CM
GAMissensep.T226Mc.677C>T1015875682UCEC
GASynonymousp.A300Ac.900C>T1015838154CM
GASynonymousp.F277Fc.831C>T1015858885CM
GASynonymousp.L21Lc.63C>T1015902236LUAD
GASynonymousp.P412Pc.1236C>T1015821093LUAD
GASynonymousp.V168Vc.504C>T1015879275CM
GT5-UTRSNV.c.1-42C>A1015902340RCCC
GTIntronicSNV.c.1028+1141C>A1015830105CLL
TAMissensep.E142Dc.426A>T1015880262RCCC
TAMissensep.Y315Fc.944A>T1015838110CM
TCMissensep.D316Gc.947A>G1015838107UCEC
TCMissensep.S284Gc.850A>G1015858866STAD