WDR61
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BRCA157858071178580711+Frame_Shift_DelDELGG-TCGA-GM-A2DD-01A-11D-A17W-09TCGA-GM-A2DD-10C-01D-A17W-09g.chr15:78580711delGc.576delCc.(574-576)cccfsp.P192fs
BRCA157858512178585121+Missense_MutationSNPCCGTCGA-D8-A27G-01A-11D-A16D-09TCGA-D8-A27G-10A-01D-A16D-09g.chr15:78585121C>Gc.156G>Cc.(154-156)gaG>gaCp.E52D
CESC157857761178577611+Nonsense_MutationSNPGGATCGA-IR-A3LK-01A-12D-A20U-09TCGA-IR-A3LK-10A-01D-A20U-09g.chr15:78577611G>Ac.820C>Tc.(820-822)Cag>Tagp.Q274*
CHOL157858071878580718+Missense_MutationSNPGGTTCGA-W5-AA2Q-01A-11D-A417-09TCGA-W5-AA2Q-10A-01D-A41A-09g.chr15:78580718G>Tc.569C>Ac.(568-570)gCc>gAcp.A190D
CHOL157858240178582401+SilentSNPAAGTCGA-W5-AA39-01A-11D-A417-09TCGA-W5-AA39-10A-01D-A41A-09g.chr15:78582401A>Gc.360T>Cc.(358-360)taT>taCp.Y120Y
COAD157857767978577679+Missense_MutationSNPGGATCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr15:78577679G>Ac.752C>Tc.(751-753)tCg>tTgp.S251L
COAD157858063978580639+SilentSNPGGATCGA-AA-3555-01A-01W-0831-10TCGA-AA-3555-10A-01W-0831-10g.chr15:78580639G>Ac.648C>Tc.(646-648)atC>atTp.I216I
COAD157858068878580688+Missense_MutationSNPGGATCGA-CM-6162-01A-11D-1650-10TCGA-CM-6162-10A-01D-1650-10g.chr15:78580688G>Ac.599C>Tc.(598-600)cCg>cTgp.P200L
COAD157858071878580718+Missense_MutationSNPGGATCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr15:78580718G>Ac.569C>Tc.(568-570)gCc>gTcp.A190V
COAD157858197778581977+SilentSNPAATTCGA-CK-4952-01A-01D-1719-10TCGA-CK-4952-10A-01D-1719-10g.chr15:78581977A>Tc.546T>Ac.(544-546)ctT>ctAp.L182L
COAD157858506678585067+Missense_MutationDNPCCCCAATCGA-AA-3697-01A-01D-1719-10TCGA-AA-3697-11A-01D-1719-10g.chr15:78585066_78585067CC>AAc.210_211GG>TTc.(208-213)gtGGac>gtTTacp.D71Y
COADREAD157857767978577679+Missense_MutationSNPGGATCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr15:78577679G>Ac.752C>Tc.(751-753)tCg>tTgp.S251L
COADREAD157858063978580639+SilentSNPGGATCGA-AA-3555-01A-01W-0831-10TCGA-AA-3555-10A-01W-0831-10g.chr15:78580639G>Ac.648C>Tc.(646-648)atC>atTp.I216I
COADREAD157858068878580688+Missense_MutationSNPGGATCGA-CM-6162-01A-11D-1650-10TCGA-CM-6162-10A-01D-1650-10g.chr15:78580688G>Ac.599C>Tc.(598-600)cCg>cTgp.P200L
COADREAD157858071878580718+Missense_MutationSNPGGATCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr15:78580718G>Ac.569C>Tc.(568-570)gCc>gTcp.A190V
COADREAD157858197778581977+SilentSNPAATTCGA-CK-4952-01A-01D-1719-10TCGA-CK-4952-10A-01D-1719-10g.chr15:78581977A>Tc.546T>Ac.(544-546)ctT>ctAp.L182L
COADREAD157858197878581978+Missense_MutationSNPAAGTCGA-F5-6465-01A-11D-1733-10TCGA-F5-6465-10A-01D-1733-10g.chr15:78581978A>Gc.545T>Cc.(544-546)cTt>cCtp.L182P
COADREAD157858506678585067+Missense_MutationDNPCCCCAATCGA-AA-3697-01A-01D-1719-10TCGA-AA-3697-11A-01D-1719-10g.chr15:78585066_78585067CC>AAc.210_211GG>TTc.(208-213)gtGGac>gtTTacp.D71Y
ESCA157858069978580699+Missense_MutationSNPCCGTCGA-IG-A51D-01A-11D-A27G-09TCGA-IG-A51D-10A-01D-A27G-09g.chr15:78580699C>Gc.588G>Cc.(586-588)ttG>ttCp.L196F
GBM157857842078578420+Missense_MutationSNPCCTTCGA-06-5858-01A-01D-1696-08TCGA-06-5858-10A-01D-1696-08g.chr15:78578420C>Tc.712G>Ac.(712-714)Gtt>Attp.V238I
GBMLGG157857842078578420+Missense_MutationSNPCCTTCGA-06-5858-01A-01D-1696-08TCGA-06-5858-10A-01D-1696-08g.chr15:78578420C>Tc.712G>Ac.(712-714)Gtt>Attp.V238I
LIHC157858230778582307+Missense_MutationSNPGGCTCGA-DD-AACZ-01A-11D-A40R-10TCGA-DD-AACZ-10A-01D-A40U-10g.chr15:78582307G>Cc.454C>Gc.(454-456)Ctt>Gttp.L152V
LUAD157857762978577629+Missense_MutationSNPGGATCGA-44-7670-01A-11D-2063-08TCGA-44-7670-10A-01D-2063-08g.chr15:78577629G>Ac.802C>Tc.(802-804)Cac>Tacp.H268Y
LUAD157858558378585583+Missense_MutationSNPCCATCGA-95-7043-01A-11D-1945-08TCGA-95-7043-10A-01D-1946-08g.chr15:78585583C>Ac.72G>Tc.(70-72)tgG>tgTp.W24C
OV157857586478575864+Splice_SiteSNPCCTTCGA-61-1895-01A-01W-0639-09TCGA-61-1895-11A-01W-0639-09g.chr15:78575864C>Tc.e11-1
OV157858197978581979+Missense_MutationSNPGGATCGA-13-0755-01A-01W-0372-09TCGA-13-0755-10A-01W-0372-09g.chr15:78581979G>Ac.544C>Tc.(544-546)Ctt>Tttp.L182F
PAAD157858511178585111+Missense_MutationSNPGGTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr15:78585111G>Tc.166C>Ac.(166-168)Cta>Atap.L56I
READ157858197878581978+Missense_MutationSNPAAGTCGA-F5-6465-01A-11D-1733-10TCGA-F5-6465-10A-01D-1733-10g.chr15:78581978A>Gc.545T>Cc.(544-546)cTt>cCtp.L182P
SKCM157858068178580681+SilentSNPGGATCGA-EE-A2MH-06A-11D-A197-08TCGA-EE-A2MH-10A-01D-A199-08g.chr15:78580681G>Ac.606C>Tc.(604-606)tcC>tcTp.S202S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US157856669978566699single base substitutionCTdownstream_gene_variant
BOCA-FR157858009578580095single base substitutionTCdownstream_gene_variant
BOCA-FR157858009578580095single base substitutionTCintron_variant
BOCA-FR157858009578580095single base substitutionTCupstream_gene_variant
BRCA-EU157856605178566051single base substitutionCTdownstream_gene_variant
BRCA-EU157856669078566690single base substitutionCTdownstream_gene_variant
BRCA-EU157857022378570223single base substitutionCT3_prime_UTR_variant
BRCA-EU157857070078570700single base substitutionTCdownstream_gene_variant
BRCA-EU157857070078570700single base substitutionTCintron_variant
BRCA-EU157857235878572363multiple base substitution (>=2bp and <=200bp)TCCTTCTGdownstream_gene_variant
BRCA-EU157857235878572363multiple base substitution (>=2bp and <=200bp)TCCTTCTGintron_variant
BRCA-EU157857273078572730single base substitutionGAdownstream_gene_variant
BRCA-EU157857273078572730single base substitutionGAintron_variant
BRCA-EU157857434978574349single base substitutionCGdownstream_gene_variant
BRCA-EU157857434978574349single base substitutionCGintron_variant
BRCA-EU157857521878575218single base substitutionGAdownstream_gene_variant
BRCA-EU157857521878575218single base substitutionGAintron_variant
BRCA-EU157857743478577434single base substitutionACdownstream_gene_variant
BRCA-EU157857743478577434single base substitutionACexon_variant
BRCA-EU157857743478577434single base substitutionACintron_variant
BRCA-EU157857817678578176single base substitutionAGdownstream_gene_variant
BRCA-EU157857817678578176single base substitutionAGexon_variant
BRCA-EU157857817678578176single base substitutionAGintron_variant
BRCA-EU157857982178579821single base substitutionCGdownstream_gene_variant
BRCA-EU157857982178579821single base substitutionCGintron_variant
BRCA-EU157857982178579821single base substitutionCGupstream_gene_variant
BRCA-EU157858046378580463single base substitutionCTdownstream_gene_variant
BRCA-EU157858046378580463single base substitutionCTintron_variant
BRCA-EU157858046378580463single base substitutionCTupstream_gene_variant
BRCA-EU157858201078582010single base substitutionGT3_prime_UTR_variant
BRCA-EU157858201078582010single base substitutionGTdownstream_gene_variant
BRCA-EU157858201078582010single base substitutionGTexon_variant
BRCA-EU157858201078582010single base substitutionGTsynonymous_variantI171I513C>A
BRCA-EU157858201078582010single base substitutionGTsynonymous_variantI41I123C>A
BRCA-EU157858201078582010single base substitutionGTsynonymous_variantI78I234C>A
BRCA-EU157858201078582010single base substitutionGTupstream_gene_variant
BRCA-EU157858201178582011single base substitutionAT3_prime_UTR_variant
BRCA-EU157858201178582011single base substitutionATdownstream_gene_variant
BRCA-EU157858201178582011single base substitutionATexon_variant
BRCA-EU157858201178582011single base substitutionATmissense_variantI171N512T>A
BRCA-EU157858201178582011single base substitutionATmissense_variantI41N122T>A
BRCA-EU157858201178582011single base substitutionATmissense_variantI78N233T>A
BRCA-EU157858201178582011single base substitutionATupstream_gene_variant
BRCA-EU157858288078582880single base substitutionCGdownstream_gene_variant
BRCA-EU157858288078582880single base substitutionCGintron_variant
BRCA-EU157858288078582880single base substitutionCGupstream_gene_variant
BRCA-EU157858317678583176single base substitutionGAdownstream_gene_variant
BRCA-EU157858317678583176single base substitutionGAintron_variant
BRCA-EU157858317678583176single base substitutionGAupstream_gene_variant
BRCA-EU157858433878584338single base substitutionTGdownstream_gene_variant
BRCA-EU157858433878584338single base substitutionTGexon_variant
BRCA-EU157858433878584338single base substitutionTGintron_variant
BRCA-EU157858433878584338single base substitutionTGupstream_gene_variant
BRCA-EU157858448578584485single base substitutionGAdownstream_gene_variant
BRCA-EU157858448578584485single base substitutionGAexon_variant
BRCA-EU157858448578584485single base substitutionGAintron_variant
BRCA-EU157858448578584485single base substitutionGAupstream_gene_variant
BRCA-EU157858450778584507single base substitutionAGdownstream_gene_variant
BRCA-EU157858450778584507single base substitutionAGexon_variant
BRCA-EU157858450778584507single base substitutionAGintron_variant
BRCA-EU157858450778584507single base substitutionAGupstream_gene_variant
BRCA-EU157858538278585386deletion of <=200bpATACC-downstream_gene_variant
BRCA-EU157858538278585386deletion of <=200bpATACC-intron_variant
BRCA-EU157858538278585386deletion of <=200bpATACC-upstream_gene_variant
BRCA-EU157858858178588581single base substitutionCGintron_variant
BRCA-EU157858877478588774single base substitutionATintron_variant
BRCA-EU157859050378590503single base substitutionCAintron_variant
BRCA-EU157859139678591396single base substitutionGTintron_variant
BRCA-EU157859193078591930single base substitutionAG5_prime_UTR_variant
BRCA-EU157859193078591930single base substitutionAGexon_variant
BRCA-EU157859193078591930single base substitutionAGupstream_gene_variant
BRCA-EU157859309778593097single base substitutionGCupstream_gene_variant
BRCA-EU157859322678593226single base substitutionGAupstream_gene_variant
BRCA-EU157859435278594352insertion of <=200bp-Tupstream_gene_variant
BRCA-FR157857022378570223single base substitutionCT3_prime_UTR_variant
BRCA-FR157857118678571186single base substitutionTGdownstream_gene_variant
BRCA-FR157857118678571186single base substitutionTGintron_variant
BRCA-FR157857262678572626single base substitutionCTdownstream_gene_variant
BRCA-FR157857262678572626single base substitutionCTintron_variant
BRCA-FR157857743478577434single base substitutionACdownstream_gene_variant
BRCA-FR157857743478577434single base substitutionACexon_variant
BRCA-FR157857743478577434single base substitutionACintron_variant
BRCA-FR157858318478583184single base substitutionCTdownstream_gene_variant
BRCA-FR157858318478583184single base substitutionCTintron_variant
BRCA-FR157858318478583184single base substitutionCTupstream_gene_variant
BRCA-FR157858433878584338single base substitutionTGdownstream_gene_variant
BRCA-FR157858433878584338single base substitutionTGexon_variant
BRCA-FR157858433878584338single base substitutionTGintron_variant
BRCA-FR157858433878584338single base substitutionTGupstream_gene_variant
BRCA-FR157859050378590503single base substitutionCAintron_variant
BRCA-UK157857521878575218single base substitutionGAdownstream_gene_variant
BRCA-UK157857521878575218single base substitutionGAintron_variant
BRCA-US157856665778566657single base substitutionCTdownstream_gene_variant
BRCA-US157856807278568072single base substitutionTCdownstream_gene_variant
BRCA-US157857266378572666deletion of <=200bpAAGT-downstream_gene_variant
BRCA-US157857266378572666deletion of <=200bpAAGT-intron_variant
BRCA-US157858071178580711deletion of <=200bpG-3_prime_UTR_variant
BRCA-US157858071178580711deletion of <=200bpG-downstream_gene_variant
BRCA-US157858071178580711deletion of <=200bpG-frameshift_variantP11
BRCA-US157858071178580711deletion of <=200bpG-frameshift_variantP192
BRCA-US157858071178580711deletion of <=200bpG-frameshift_variantP62
BRCA-US157858071178580711deletion of <=200bpG-frameshift_variantP99
BRCA-US157858071178580711deletion of <=200bpG-upstream_gene_variant
BRCA-US157858512178585121single base substitutionCG3_prime_UTR_variant
BRCA-US157858512178585121single base substitutionCGdownstream_gene_variant
BRCA-US157858512178585121single base substitutionCGexon_variant
BRCA-US157858512178585121single base substitutionCGintron_variant
BRCA-US157858512178585121single base substitutionCGmissense_variantE52D156G>C
BRCA-US157858512178585121single base substitutionCGupstream_gene_variant
BTCA-JP157856541478565414single base substitutionAGdownstream_gene_variant
BTCA-JP157857046278570462single base substitutionTCintron_variant
BTCA-JP157857281178572811single base substitutionGAdownstream_gene_variant
BTCA-JP157857281178572811single base substitutionGAintron_variant
BTCA-JP157858121278581212single base substitutionTC3_prime_UTR_variant
BTCA-JP157858121278581212single base substitutionTCdownstream_gene_variant
BTCA-JP157858121278581212single base substitutionTCintron_variant
BTCA-JP157858121278581212single base substitutionTCupstream_gene_variant
BTCA-JP157858236378582363single base substitutionAG3_prime_UTR_variant
BTCA-JP157858236378582363single base substitutionAGdownstream_gene_variant
BTCA-JP157858236378582363single base substitutionAGexon_variant
BTCA-JP157858236378582363single base substitutionAGmissense_variantF133S398T>C
BTCA-JP157858236378582363single base substitutionAGmissense_variantF3S8T>C
BTCA-JP157858236378582363single base substitutionAGmissense_variantF40S119T>C
BTCA-JP157858236378582363single base substitutionAGupstream_gene_variant
CESC-US157857761178577611single base substitutionGAdownstream_gene_variant
CESC-US157857761178577611single base substitutionGAexon_variant
CESC-US157857761178577611single base substitutionGAintron_variant
CESC-US157857761178577611single base substitutionGAstop_gainedQ144*430C>T
CESC-US157857761178577611single base substitutionGAstop_gainedQ181*541C>T
CESC-US157857761178577611single base substitutionGAstop_gainedQ274*820C>T
CLLE-ES157856566578565665single base substitutionCAdownstream_gene_variant
CLLE-ES157857050578570505single base substitutionTGintron_variant
CLLE-ES157858365478583654single base substitutionGTdownstream_gene_variant
CLLE-ES157858365478583654single base substitutionGTintron_variant
CLLE-ES157858365478583654single base substitutionGTupstream_gene_variant
CLLE-ES157859149778591497single base substitutionGCintron_variant
COAD-US157856657578566575single base substitutionCTdownstream_gene_variant
COAD-US157856673478566736deletion of <=200bpAGA-downstream_gene_variant
COAD-US157856785378567853single base substitutionGTdownstream_gene_variant
COAD-US157856802378568023single base substitutionCTdownstream_gene_variant
COAD-US157856804478568044single base substitutionGAdownstream_gene_variant
COAD-US157858068878580688single base substitutionGA3_prime_UTR_variant
COAD-US157858068878580688single base substitutionGAdownstream_gene_variant
COAD-US157858068878580688single base substitutionGAmissense_variantP107L320C>T
COAD-US157858068878580688single base substitutionGAmissense_variantP19L56C>T
COAD-US157858068878580688single base substitutionGAmissense_variantP200L599C>T
COAD-US157858068878580688single base substitutionGAmissense_variantP70L209C>T
COAD-US157858068878580688single base substitutionGAupstream_gene_variant
COAD-US157858071878580718single base substitutionGA3_prime_UTR_variant
COAD-US157858071878580718single base substitutionGAdownstream_gene_variant
COAD-US157858071878580718single base substitutionGAmissense_variantA190V569C>T
COAD-US157858071878580718single base substitutionGAmissense_variantA60V179C>T
COAD-US157858071878580718single base substitutionGAmissense_variantA97V290C>T
COAD-US157858071878580718single base substitutionGAmissense_variantA9V26C>T
COAD-US157858071878580718single base substitutionGAupstream_gene_variant
COAD-US157858239778582397single base substitutionCT3_prime_UTR_variant
COAD-US157858239778582397single base substitutionCTdownstream_gene_variant
COAD-US157858239778582397single base substitutionCTexon_variant
COAD-US157858239778582397single base substitutionCTmissense_variantA122T364G>A
COAD-US157858239778582397single base substitutionCTmissense_variantA29T85G>A
COAD-US157858239778582397single base substitutionCTupstream_gene_variant
COAD-US157858506678585066single base substitutionCA3_prime_UTR_variant
COAD-US157858506678585066single base substitutionCAdownstream_gene_variant
COAD-US157858506678585066single base substitutionCAexon_variant
COAD-US157858506678585066single base substitutionCAintron_variant
COAD-US157858506678585066single base substitutionCAmissense_variantD71Y211G>T
COAD-US157858506678585066single base substitutionCAupstream_gene_variant
COAD-US157858506778585067single base substitutionCA3_prime_UTR_variant
COAD-US157858506778585067single base substitutionCAdownstream_gene_variant
COAD-US157858506778585067single base substitutionCAexon_variant
COAD-US157858506778585067single base substitutionCAintron_variant
COAD-US157858506778585067single base substitutionCAsynonymous_variantV70V210G>T
COAD-US157858506778585067single base substitutionCAupstream_gene_variant
COCA-CN157857276078572760single base substitutionCTdownstream_gene_variant
COCA-CN157857276078572760single base substitutionCTintron_variant
COCA-CN157857770978577709single base substitutionGAdownstream_gene_variant
COCA-CN157857770978577709single base substitutionGAexon_variant
COCA-CN157857770978577709single base substitutionGAintron_variant
COCA-CN157857848578578485single base substitutionGAdownstream_gene_variant
COCA-CN157857848578578485single base substitutionGAexon_variant
COCA-CN157857848578578485single base substitutionGAintron_variant
COCA-CN157857848578578485single base substitutionGAupstream_gene_variant
COCA-CN157858184078581840single base substitutionTCdownstream_gene_variant
COCA-CN157858184078581840single base substitutionTCintron_variant
COCA-CN157858184078581840single base substitutionTCupstream_gene_variant
COCA-CN157858230878582308single base substitutionAG3_prime_UTR_variant
COCA-CN157858230878582308single base substitutionAGdownstream_gene_variant
COCA-CN157858230878582308single base substitutionAGexon_variant
COCA-CN157858230878582308single base substitutionAGsynonymous_variantI151I453T>C
COCA-CN157858230878582308single base substitutionAGsynonymous_variantI21I63T>C
COCA-CN157858230878582308single base substitutionAGsynonymous_variantI58I174T>C
COCA-CN157858230878582308single base substitutionAGupstream_gene_variant
EOPC-DE157857207778572077single base substitutionGAdownstream_gene_variant
EOPC-DE157857207778572077single base substitutionGAintron_variant
ESAD-UK157856540878565408single base substitutionGAdownstream_gene_variant
ESAD-UK157856626278566262single base substitutionCTdownstream_gene_variant
ESAD-UK157856638378566383single base substitutionCTdownstream_gene_variant
ESAD-UK157857017878570178single base substitutionCT3_prime_UTR_variant
ESAD-UK157857206078572060single base substitutionGAdownstream_gene_variant
ESAD-UK157857206078572060single base substitutionGAintron_variant
ESAD-UK157857347278573472single base substitutionCTdownstream_gene_variant
ESAD-UK157857347278573472single base substitutionCTintron_variant
ESAD-UK157857629478576294single base substitutionCTdownstream_gene_variant
ESAD-UK157857629478576294single base substitutionCTexon_variant
ESAD-UK157857629478576294single base substitutionCTintron_variant
ESAD-UK157857887778578877single base substitutionCTdownstream_gene_variant
ESAD-UK157857887778578877single base substitutionCTexon_variant
ESAD-UK157857887778578877single base substitutionCTintron_variant
ESAD-UK157857887778578877single base substitutionCTupstream_gene_variant
ESAD-UK157857913378579133single base substitutionGAdownstream_gene_variant
ESAD-UK157857913378579133single base substitutionGAexon_variant
ESAD-UK157857913378579133single base substitutionGAintron_variant
ESAD-UK157857913378579133single base substitutionGAupstream_gene_variant
ESAD-UK157858016978580169single base substitutionCTdownstream_gene_variant
ESAD-UK157858016978580169single base substitutionCTintron_variant
ESAD-UK157858016978580169single base substitutionCTupstream_gene_variant
ESAD-UK157858492678584926single base substitutionTGdownstream_gene_variant
ESAD-UK157858492678584926single base substitutionTGexon_variant
ESAD-UK157858492678584926single base substitutionTGintron_variant
ESAD-UK157858492678584926single base substitutionTGupstream_gene_variant
ESAD-UK157858611678586116single base substitutionTCdownstream_gene_variant
ESAD-UK157858611678586116single base substitutionTCintron_variant
ESAD-UK157858611678586116single base substitutionTCupstream_gene_variant
ESAD-UK157858846778588467single base substitutionCTintron_variant
ESAD-UK157859015878590158single base substitutionCAintron_variant
ESAD-UK157859115978591159single base substitutionTAintron_variant
ESAD-UK157859138778591387single base substitutionTGintron_variant
ESAD-UK157859224978592249single base substitutionATupstream_gene_variant
ESAD-UK157859279478592794single base substitutionAGupstream_gene_variant
ESAD-UK157859334178593341single base substitutionTGupstream_gene_variant
ESAD-UK157859334578593345single base substitutionGTupstream_gene_variant
ESAD-UK157859367678593676single base substitutionGTupstream_gene_variant
ESAD-UK157859409678594096single base substitutionTCupstream_gene_variant
ESAD-UK157859422278594222single base substitutionGAupstream_gene_variant
ESAD-UK157859453778594537single base substitutionGAupstream_gene_variant
ESAD-UK157859680178596801single base substitutionATupstream_gene_variant
ESCA-CN157856797378567973single base substitutionCAdownstream_gene_variant
ESCA-CN157858184078581840single base substitutionTCdownstream_gene_variant
ESCA-CN157858184078581840single base substitutionTCintron_variant
ESCA-CN157858184078581840single base substitutionTCupstream_gene_variant
ESCA-CN157858201878582018single base substitutionCT3_prime_UTR_variant
ESCA-CN157858201878582018single base substitutionCTdownstream_gene_variant
ESCA-CN157858201878582018single base substitutionCTexon_variant
ESCA-CN157858201878582018single base substitutionCTmissense_variantD169N505G>A
ESCA-CN157858201878582018single base substitutionCTmissense_variantD39N115G>A
ESCA-CN157858201878582018single base substitutionCTmissense_variantD76N226G>A
ESCA-CN157858201878582018single base substitutionCTupstream_gene_variant
GBM-US157856795078567950single base substitutionCGdownstream_gene_variant
GBM-US157857842078578420single base substitutionCTdownstream_gene_variant
GBM-US157857842078578420single base substitutionCTexon_variant
GBM-US157857842078578420single base substitutionCTintron_variant
GBM-US157857842078578420single base substitutionCTmissense_variantV108I322G>A
GBM-US157857842078578420single base substitutionCTmissense_variantV145I433G>A
GBM-US157857842078578420single base substitutionCTmissense_variantV238I712G>A
GBM-US157857842078578420single base substitutionCTupstream_gene_variant
KIRC-US157856545078565450single base substitutionAGdownstream_gene_variant
LAML-KR157859255478592554single base substitutionAGupstream_gene_variant
LICA-FR157857180678571806single base substitutionCAdownstream_gene_variant
LICA-FR157857180678571806single base substitutionCAintron_variant
LICA-FR157857728178577281single base substitutionCAdownstream_gene_variant
LICA-FR157857728178577281single base substitutionCAexon_variant
LICA-FR157857728178577281single base substitutionCAintron_variant
LICA-FR157858343878583438single base substitutionTCdownstream_gene_variant
LICA-FR157858343878583438single base substitutionTCintron_variant
LICA-FR157858343878583438single base substitutionTCupstream_gene_variant
LICA-FR157858609978586099single base substitutionATdownstream_gene_variant
LICA-FR157858609978586099single base substitutionATintron_variant
LICA-FR157858609978586099single base substitutionATupstream_gene_variant
LICA-FR157859277578592775insertion of <=200bp-Aupstream_gene_variant
LICA-FR157859537978595379single base substitutionATupstream_gene_variant
LINC-JP157857066978570669single base substitutionAGdownstream_gene_variant
LINC-JP157857066978570669single base substitutionAGintron_variant
LINC-JP157857073278570732single base substitutionTCdownstream_gene_variant
LINC-JP157857073278570732single base substitutionTCintron_variant
LINC-JP157857213978572139single base substitutionCTdownstream_gene_variant
LINC-JP157857213978572139single base substitutionCTintron_variant
LINC-JP157857502478575024single base substitutionTAdownstream_gene_variant
LINC-JP157857502478575024single base substitutionTAintron_variant
LINC-JP157858317078583170single base substitutionGTdownstream_gene_variant
LINC-JP157858317078583170single base substitutionGTintron_variant
LINC-JP157858317078583170single base substitutionGTupstream_gene_variant
LINC-JP157858663378586633single base substitutionCTdownstream_gene_variant
LINC-JP157858663378586633single base substitutionCTintron_variant
LINC-JP157858663378586633single base substitutionCTupstream_gene_variant
LINC-JP157858721778587217single base substitutionAGexon_variant
LINC-JP157858721778587217single base substitutionAGintron_variant
LINC-JP157858721778587217single base substitutionAGupstream_gene_variant
LINC-JP157858776178587761single base substitutionGTexon_variant
LINC-JP157858776178587761single base substitutionGTintron_variant
LIRI-JP157856703778567037single base substitutionAGdownstream_gene_variant
LIRI-JP157856724178567241single base substitutionTCdownstream_gene_variant
LIRI-JP157856904478569044single base substitutionCAdownstream_gene_variant
LIRI-JP157857022378570223single base substitutionCG3_prime_UTR_variant
LIRI-JP157857517178575171single base substitutionTCdownstream_gene_variant
LIRI-JP157857517178575171single base substitutionTCintron_variant
LIRI-JP157858233178582331single base substitutionAG3_prime_UTR_variant
LIRI-JP157858233178582331single base substitutionAGdownstream_gene_variant
LIRI-JP157858233178582331single base substitutionAGexon_variant
LIRI-JP157858233178582331single base substitutionAGsynonymous_variantL144L430T>C
LIRI-JP157858233178582331single base substitutionAGsynonymous_variantL14L40T>C
LIRI-JP157858233178582331single base substitutionAGsynonymous_variantL51L151T>C
LIRI-JP157858233178582331single base substitutionAGupstream_gene_variant
LIRI-JP157858239478582394single base substitutionTC3_prime_UTR_variant
LIRI-JP157858239478582394single base substitutionTCdownstream_gene_variant
LIRI-JP157858239478582394single base substitutionTCexon_variant
LIRI-JP157858239478582394single base substitutionTCmissense_variantT123A367A>G
LIRI-JP157858239478582394single base substitutionTCmissense_variantT30A88A>G
LIRI-JP157858239478582394single base substitutionTCupstream_gene_variant
LIRI-JP157858300878583008single base substitutionATdownstream_gene_variant
LIRI-JP157858300878583008single base substitutionATintron_variant
LIRI-JP157858300878583008single base substitutionATupstream_gene_variant
LIRI-JP157858492578584925single base substitutionCTdownstream_gene_variant
LIRI-JP157858492578584925single base substitutionCTexon_variant
LIRI-JP157858492578584925single base substitutionCTintron_variant
LIRI-JP157858492578584925single base substitutionCTupstream_gene_variant
LIRI-JP157858617978586179single base substitutionGAdownstream_gene_variant
LIRI-JP157858617978586179single base substitutionGAintron_variant
LIRI-JP157858617978586179single base substitutionGAupstream_gene_variant
LIRI-JP157858795478587954single base substitutionCGexon_variant
LIRI-JP157858795478587954single base substitutionCGintron_variant
LIRI-JP157858933678589336single base substitutionATintron_variant
LIRI-JP157859141278591412single base substitutionGAintron_variant
LIRI-JP157859217378592173single base substitutionGTupstream_gene_variant
LIRI-JP157859218278592182single base substitutionGCupstream_gene_variant
LIRI-JP157859467878594678single base substitutionCGupstream_gene_variant
LIRI-JP157859479578594795single base substitutionGAupstream_gene_variant
LUSC-KR157856547878565478single base substitutionCTdownstream_gene_variant
LUSC-KR157856561678565616single base substitutionAGdownstream_gene_variant
LUSC-KR157856580478565804single base substitutionGCdownstream_gene_variant
LUSC-KR157856684078566840single base substitutionCGdownstream_gene_variant
LUSC-KR157856852578568525single base substitutionTGdownstream_gene_variant
LUSC-KR157857374578573745single base substitutionGCdownstream_gene_variant
LUSC-KR157857374578573745single base substitutionGCintron_variant
LUSC-KR157857397678573976single base substitutionGTdownstream_gene_variant
LUSC-KR157857397678573976single base substitutionGTintron_variant
LUSC-KR157857928078579280single base substitutionGAdownstream_gene_variant
LUSC-KR157857928078579280single base substitutionGAintron_variant
LUSC-KR157857928078579280single base substitutionGAupstream_gene_variant
LUSC-KR157858981778589817single base substitutionCGintron_variant
MALY-DE157858330378583303single base substitutionATdownstream_gene_variant
MALY-DE157858330378583303single base substitutionATintron_variant
MALY-DE157858330378583303single base substitutionATupstream_gene_variant
MALY-DE157859334378593343single base substitutionGTupstream_gene_variant
MALY-DE157859452678594526single base substitutionTGupstream_gene_variant
MELA-AU157856589978565899single base substitutionGTdownstream_gene_variant
MELA-AU157856654978566549single base substitutionGAdownstream_gene_variant
MELA-AU157857039878570398single base substitutionCT3_prime_UTR_variant
MELA-AU157857220578572205single base substitutionCTdownstream_gene_variant
MELA-AU157857220578572205single base substitutionCTintron_variant
MELA-AU157857361778573617single base substitutionCAdownstream_gene_variant
MELA-AU157857361778573617single base substitutionCAintron_variant
MELA-AU157857443778574437single base substitutionCTdownstream_gene_variant
MELA-AU157857443778574437single base substitutionCTintron_variant
MELA-AU157857461578574615single base substitutionGTdownstream_gene_variant
MELA-AU157857461578574615single base substitutionGTintron_variant
MELA-AU157857462878574628single base substitutionGTdownstream_gene_variant
MELA-AU157857462878574628single base substitutionGTintron_variant
MELA-AU157857671178576711single base substitutionGAdownstream_gene_variant
MELA-AU157857671178576711single base substitutionGAexon_variant
MELA-AU157857671178576711single base substitutionGAintron_variant
MELA-AU157857819378578193single base substitutionGAdownstream_gene_variant
MELA-AU157857819378578193single base substitutionGAexon_variant
MELA-AU157857819378578193single base substitutionGAintron_variant
MELA-AU157857877478578774single base substitutionCTdownstream_gene_variant
MELA-AU157857877478578774single base substitutionCTexon_variant
MELA-AU157857877478578774single base substitutionCTintron_variant
MELA-AU157857877478578774single base substitutionCTupstream_gene_variant
MELA-AU157857887278578872single base substitutionCTdownstream_gene_variant
MELA-AU157857887278578872single base substitutionCTexon_variant
MELA-AU157857887278578872single base substitutionCTintron_variant
MELA-AU157857887278578872single base substitutionCTupstream_gene_variant
MELA-AU157857946678579466single base substitutionGAdownstream_gene_variant
MELA-AU157857946678579466single base substitutionGAintron_variant
MELA-AU157857946678579466single base substitutionGAupstream_gene_variant
MELA-AU157857958078579580single base substitutionCTdownstream_gene_variant
MELA-AU157857958078579580single base substitutionCTintron_variant
MELA-AU157857958078579580single base substitutionCTupstream_gene_variant
MELA-AU157857995278579952single base substitutionGCdownstream_gene_variant
MELA-AU157857995278579952single base substitutionGCintron_variant
MELA-AU157857995278579952single base substitutionGCupstream_gene_variant
MELA-AU157858049278580492single base substitutionGAdownstream_gene_variant
MELA-AU157858049278580492single base substitutionGAintron_variant
MELA-AU157858049278580492single base substitutionGAupstream_gene_variant
MELA-AU157858068178580681single base substitutionGA3_prime_UTR_variant
MELA-AU157858068178580681single base substitutionGAdownstream_gene_variant
MELA-AU157858068178580681single base substitutionGAsynonymous_variantS109S327C>T
MELA-AU157858068178580681single base substitutionGAsynonymous_variantS202S606C>T
MELA-AU157858068178580681single base substitutionGAsynonymous_variantS21S63C>T
MELA-AU157858068178580681single base substitutionGAsynonymous_variantS72S216C>T
MELA-AU157858068178580681single base substitutionGAupstream_gene_variant
MELA-AU157858085778580857single base substitutionGAdownstream_gene_variant
MELA-AU157858085778580857single base substitutionGAintron_variant
MELA-AU157858085778580857single base substitutionGAupstream_gene_variant
MELA-AU157858237778582377single base substitutionCG3_prime_UTR_variant
MELA-AU157858237778582377single base substitutionCGdownstream_gene_variant
MELA-AU157858237778582377single base substitutionCGexon_variant
MELA-AU157858237778582377single base substitutionCGsynonymous_variantG128G384G>C
MELA-AU157858237778582377single base substitutionCGsynonymous_variantG35G105G>C
MELA-AU157858237778582377single base substitutionCGupstream_gene_variant
MELA-AU157858253878582538single base substitutionGAdownstream_gene_variant
MELA-AU157858253878582538single base substitutionGAintron_variant
MELA-AU157858253878582538single base substitutionGAupstream_gene_variant
MELA-AU157858282078582820single base substitutionGAdownstream_gene_variant
MELA-AU157858282078582820single base substitutionGAintron_variant
MELA-AU157858282078582820single base substitutionGAupstream_gene_variant
MELA-AU157858286978582870multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU157858286978582870multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU157858286978582870multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU157858342578583425single base substitutionTAdownstream_gene_variant
MELA-AU157858342578583425single base substitutionTAintron_variant
MELA-AU157858342578583425single base substitutionTAupstream_gene_variant
MELA-AU157858404178584041single base substitutionGAdownstream_gene_variant
MELA-AU157858404178584041single base substitutionGAintron_variant
MELA-AU157858404178584041single base substitutionGAupstream_gene_variant
MELA-AU157858415678584156single base substitutionGAdownstream_gene_variant
MELA-AU157858415678584156single base substitutionGAexon_variant
MELA-AU157858415678584156single base substitutionGAintron_variant
MELA-AU157858415678584156single base substitutionGAupstream_gene_variant
MELA-AU157858450178584501single base substitutionGAdownstream_gene_variant
MELA-AU157858450178584501single base substitutionGAexon_variant
MELA-AU157858450178584501single base substitutionGAintron_variant
MELA-AU157858450178584501single base substitutionGAupstream_gene_variant
MELA-AU157858509478585094single base substitutionCT3_prime_UTR_variant
MELA-AU157858509478585094single base substitutionCTdownstream_gene_variant
MELA-AU157858509478585094single base substitutionCTexon_variant
MELA-AU157858509478585094single base substitutionCTintron_variant
MELA-AU157858509478585094single base substitutionCTsynonymous_variantE61E183G>A
MELA-AU157858509478585094single base substitutionCTupstream_gene_variant
MELA-AU157858585978585859single base substitutionAGdownstream_gene_variant
MELA-AU157858585978585859single base substitutionAGintron_variant
MELA-AU157858585978585859single base substitutionAGupstream_gene_variant
MELA-AU157858668478586684single base substitutionGAdownstream_gene_variant
MELA-AU157858668478586684single base substitutionGAintron_variant
MELA-AU157858668478586684single base substitutionGAupstream_gene_variant
MELA-AU157858669178586691single base substitutionGAdownstream_gene_variant
MELA-AU157858669178586691single base substitutionGAintron_variant
MELA-AU157858669178586691single base substitutionGAupstream_gene_variant
MELA-AU157858749978587499single base substitutionCAexon_variant
MELA-AU157858749978587499single base substitutionCAintron_variant
MELA-AU157858892878588928single base substitutionTCintron_variant
MELA-AU157858897778588977single base substitutionGAintron_variant
MELA-AU157858928178589282multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU157859053278590532single base substitutionCTintron_variant
MELA-AU157859061778590617single base substitutionATintron_variant
MELA-AU157859084678590846single base substitutionGAintron_variant
MELA-AU157859126878591268single base substitutionGAintron_variant
MELA-AU157859281378592813single base substitutionGAupstream_gene_variant
MELA-AU157859288478592884single base substitutionGAupstream_gene_variant
MELA-AU157859336878593368single base substitutionCTupstream_gene_variant
MELA-AU157859359478593594single base substitutionGAupstream_gene_variant
MELA-AU157859374578593745single base substitutionGAupstream_gene_variant
MELA-AU157859388378593883single base substitutionCTupstream_gene_variant
MELA-AU157859402578594025single base substitutionCAupstream_gene_variant
MELA-AU157859490078594900single base substitutionATupstream_gene_variant
MELA-AU157859643078596430single base substitutionCTupstream_gene_variant
MELA-AU157859678378596783single base substitutionCGupstream_gene_variant
MELA-AU157859685378596853single base substitutionGAupstream_gene_variant
MELA-AU157859698978596989single base substitutionGAupstream_gene_variant
MELA-AU157859712578597125single base substitutionGAupstream_gene_variant
OV-AU157856673478566736deletion of <=200bpAGA-downstream_gene_variant
OV-AU157857047778570477single base substitutionGAintron_variant
OV-AU157857140978571409single base substitutionCAdownstream_gene_variant
OV-AU157857140978571409single base substitutionCAintron_variant
OV-AU157858401078584010single base substitutionTGdownstream_gene_variant
OV-AU157858401078584010single base substitutionTGintron_variant
OV-AU157858401078584010single base substitutionTGupstream_gene_variant
OV-AU157858401378584013single base substitutionGAdownstream_gene_variant
OV-AU157858401378584013single base substitutionGAintron_variant
OV-AU157858401378584013single base substitutionGAupstream_gene_variant
OV-AU157859387378593873single base substitutionCTupstream_gene_variant
OV-AU157859658178596581single base substitutionATupstream_gene_variant
OV-US157858197978581979single base substitutionGA3_prime_UTR_variant
OV-US157858197978581979single base substitutionGAdownstream_gene_variant
OV-US157858197978581979single base substitutionGAexon_variant
OV-US157858197978581979single base substitutionGAmissense_variantL182F544C>T
OV-US157858197978581979single base substitutionGAmissense_variantL1F1C>T
OV-US157858197978581979single base substitutionGAmissense_variantL52F154C>T
OV-US157858197978581979single base substitutionGAmissense_variantL89F265C>T
OV-US157858197978581979single base substitutionGAupstream_gene_variant
PACA-AU157858592678585926single base substitutionCTdownstream_gene_variant
PACA-AU157858592678585926single base substitutionCTintron_variant
PACA-AU157858592678585926single base substitutionCTupstream_gene_variant
PACA-AU157859085478590854single base substitutionAGintron_variant
PACA-AU157859334178593341single base substitutionTGupstream_gene_variant
PACA-CA157856678278566782single base substitutionGAdownstream_gene_variant
PACA-CA157857035778570357single base substitutionCG3_prime_UTR_variant
PACA-CA157857220578572205single base substitutionCAdownstream_gene_variant
PACA-CA157857220578572205single base substitutionCAintron_variant
PACA-CA157857246378572463single base substitutionAGdownstream_gene_variant
PACA-CA157857246378572463single base substitutionAGintron_variant
PACA-CA157857307778573077single base substitutionGAdownstream_gene_variant
PACA-CA157857307778573077single base substitutionGAintron_variant
PACA-CA157857694678576946single base substitutionCAdownstream_gene_variant
PACA-CA157857694678576946single base substitutionCAexon_variant
PACA-CA157857694678576946single base substitutionCAintron_variant
PACA-CA157858578078585780single base substitutionAGdownstream_gene_variant
PACA-CA157858578078585780single base substitutionAGintron_variant
PACA-CA157858578078585780single base substitutionAGupstream_gene_variant
PACA-CA157859252178592521single base substitutionGAupstream_gene_variant
PACA-CA157859334378593343single base substitutionGTupstream_gene_variant
PACA-CA157859640178596401single base substitutionGAupstream_gene_variant
PAEN-AU157859659078596590single base substitutionCAupstream_gene_variant
PAEN-IT157858571078585710single base substitutionATdownstream_gene_variant
PAEN-IT157858571078585710single base substitutionATintron_variant
PAEN-IT157858571078585710single base substitutionATupstream_gene_variant
PBCA-DE157857902378579023single base substitutionACdownstream_gene_variant
PBCA-DE157857902378579023single base substitutionACexon_variant
PBCA-DE157857902378579023single base substitutionACintron_variant
PBCA-DE157857902378579023single base substitutionACupstream_gene_variant
PBCA-DE157858563078585630single base substitutionCAdownstream_gene_variant
PBCA-DE157858563078585630single base substitutionCAintron_variant
PBCA-DE157858563078585630single base substitutionCAupstream_gene_variant
PBCA-DE157859242178592421single base substitutionGCupstream_gene_variant
PBCA-DE157859270278592702single base substitutionGAupstream_gene_variant
PBCA-DE157859365678593656single base substitutionCTupstream_gene_variant
PRAD-CA157856933978569339single base substitutionTCdownstream_gene_variant
PRAD-CA157856946078569460single base substitutionGAdownstream_gene_variant
PRAD-UK157856669878566698single base substitutionGCdownstream_gene_variant
PRAD-UK157857937378579375deletion of <=200bpAAT-downstream_gene_variant
PRAD-UK157857937378579375deletion of <=200bpAAT-intron_variant
PRAD-UK157857937378579375deletion of <=200bpAAT-upstream_gene_variant
PRAD-UK157858138278581382single base substitutionCTdownstream_gene_variant
PRAD-UK157858138278581382single base substitutionCTintron_variant
PRAD-UK157858138278581382single base substitutionCTupstream_gene_variant
PRAD-UK157858515278585152single base substitutionTG3_prime_UTR_variant
PRAD-UK157858515278585152single base substitutionTGdownstream_gene_variant
PRAD-UK157858515278585152single base substitutionTGexon_variant
PRAD-UK157858515278585152single base substitutionTGintron_variant
PRAD-UK157858515278585152single base substitutionTGupstream_gene_variant
PRAD-UK157858549478585494single base substitutionGCdownstream_gene_variant
PRAD-UK157858549478585494single base substitutionGCintron_variant
PRAD-UK157858549478585494single base substitutionGCupstream_gene_variant
PRAD-UK157859026978590269single base substitutionTCintron_variant
RECA-EU157856707778567077single base substitutionCTdownstream_gene_variant
RECA-EU157857552778575527single base substitutionCTdownstream_gene_variant
RECA-EU157857552778575527single base substitutionCTintron_variant
RECA-EU157858516478585164single base substitutionCT3_prime_UTR_variant
RECA-EU157858516478585164single base substitutionCTdownstream_gene_variant
RECA-EU157858516478585164single base substitutionCTexon_variant
RECA-EU157858516478585164single base substitutionCTintron_variant
RECA-EU157858516478585164single base substitutionCTupstream_gene_variant
RECA-EU157859251378592513single base substitutionTCupstream_gene_variant
SKCA-BR157857038478570384single base substitutionTC3_prime_UTR_variant
SKCA-BR157857607278576073deletion of <=200bpCA-downstream_gene_variant
SKCA-BR157857607278576073deletion of <=200bpCA-exon_variant
SKCA-BR157857607278576073deletion of <=200bpCA-intron_variant
SKCA-BR157857629578576295insertion of <=200bp-GCdownstream_gene_variant
SKCA-BR157857629578576295insertion of <=200bp-GCexon_variant
SKCA-BR157857629578576295insertion of <=200bp-GCintron_variant
SKCA-BR157857789778577897single base substitutionCTdownstream_gene_variant
SKCA-BR157857789778577897single base substitutionCTexon_variant
SKCA-BR157857789778577897single base substitutionCTintron_variant
SKCA-BR157857807178578071single base substitutionATdownstream_gene_variant
SKCA-BR157857807178578071single base substitutionATexon_variant
SKCA-BR157857807178578071single base substitutionATintron_variant
SKCA-BR157857807178578071single base substitutionATsplice_region_variant
SKCA-BR157857818578578185single base substitutionGAdownstream_gene_variant
SKCA-BR157857818578578185single base substitutionGAexon_variant
SKCA-BR157857818578578185single base substitutionGAintron_variant
SKCA-BR157857848378578483single base substitutionGTdownstream_gene_variant
SKCA-BR157857848378578483single base substitutionGTexon_variant
SKCA-BR157857848378578483single base substitutionGTintron_variant
SKCA-BR157857848378578483single base substitutionGTsplice_region_variant
SKCA-BR157857848378578483single base substitutionGTupstream_gene_variant
SKCA-BR157858299478582994single base substitutionGAdownstream_gene_variant
SKCA-BR157858299478582994single base substitutionGAintron_variant
SKCA-BR157858299478582994single base substitutionGAupstream_gene_variant
SKCA-BR157858315878583158insertion of <=200bp-CTTdownstream_gene_variant
SKCA-BR157858315878583158insertion of <=200bp-CTTintron_variant
SKCA-BR157858315878583158insertion of <=200bp-CTTupstream_gene_variant
SKCA-BR157858501278585012single base substitutionGA3_prime_UTR_variant
SKCA-BR157858501278585012single base substitutionGAdownstream_gene_variant
SKCA-BR157858501278585012single base substitutionGAexon_variant
SKCA-BR157858501278585012single base substitutionGAintron_variant
SKCA-BR157858501278585012single base substitutionGAmissense_variantR89C265C>T
SKCA-BR157858501278585012single base substitutionGAupstream_gene_variant
SKCA-BR157858679478586794single base substitutionTCdownstream_gene_variant
SKCA-BR157858679478586794single base substitutionTCintron_variant
SKCA-BR157858679478586794single base substitutionTCupstream_gene_variant
SKCA-BR157858901778589017single base substitutionTAintron_variant
SKCA-BR157859099778590997single base substitutionTCintron_variant
SKCA-BR157859241578592415single base substitutionTGupstream_gene_variant
SKCA-BR157859576778595768deletion of <=200bpCT-upstream_gene_variant
SKCA-BR157859593078595930single base substitutionGAupstream_gene_variant
SKCA-BR157859644178596441single base substitutionGAupstream_gene_variant
SKCA-BR157859644278596442single base substitutionGAupstream_gene_variant
SKCM-US157856784478567844single base substitutionGAdownstream_gene_variant
SKCM-US157856797378567973single base substitutionCTdownstream_gene_variant
SKCM-US157858068178580681single base substitutionGA3_prime_UTR_variant
SKCM-US157858068178580681single base substitutionGAdownstream_gene_variant
SKCM-US157858068178580681single base substitutionGAsynonymous_variantS109S327C>T
SKCM-US157858068178580681single base substitutionGAsynonymous_variantS202S606C>T
SKCM-US157858068178580681single base substitutionGAsynonymous_variantS21S63C>T
SKCM-US157858068178580681single base substitutionGAsynonymous_variantS72S216C>T
SKCM-US157858068178580681single base substitutionGAupstream_gene_variant
STAD-US157856664078566640single base substitutionAGdownstream_gene_variant
STAD-US157856664878566648single base substitutionCTdownstream_gene_variant
STAD-US157856804478568044single base substitutionGAdownstream_gene_variant
STAD-US157858201378582013single base substitutionTC3_prime_UTR_variant
STAD-US157858201378582013single base substitutionTCdownstream_gene_variant
STAD-US157858201378582013single base substitutionTCexon_variant
STAD-US157858201378582013single base substitutionTCsynonymous_variantG170G510A>G
STAD-US157858201378582013single base substitutionTCsynonymous_variantG40G120A>G
STAD-US157858201378582013single base substitutionTCsynonymous_variantG77G231A>G
STAD-US157858201378582013single base substitutionTCupstream_gene_variant
STAD-US157858204578582045single base substitutionCA3_prime_UTR_variant
STAD-US157858204578582045single base substitutionCAdownstream_gene_variant
STAD-US157858204578582045single base substitutionCAexon_variant
STAD-US157858204578582045single base substitutionCAmissense_variantG160W478G>T
STAD-US157858204578582045single base substitutionCAmissense_variantG30W88G>T
STAD-US157858204578582045single base substitutionCAmissense_variantG67W199G>T
STAD-US157858204578582045single base substitutionCAupstream_gene_variant
THCA-SA157857374578573745single base substitutionGCdownstream_gene_variant
THCA-SA157857374578573745single base substitutionGCintron_variant
THCA-SA157858510678585106single base substitutionCT3_prime_UTR_variant
THCA-SA157858510678585106single base substitutionCTdownstream_gene_variant
THCA-SA157858510678585106single base substitutionCTexon_variant
THCA-SA157858510678585106single base substitutionCTintron_variant
THCA-SA157858510678585106single base substitutionCTsynonymous_variantQ57Q171G>A
THCA-SA157858510678585106single base substitutionCTupstream_gene_variant
UCEC-US157856544178565441single base substitutionGAdownstream_gene_variant
UCEC-US157856668078566680single base substitutionGAdownstream_gene_variant
UCEC-US157856674478566744single base substitutionTCdownstream_gene_variant
UCEC-US157856804478568044single base substitutionGAdownstream_gene_variant
UCEC-US157856805278568052single base substitutionGAdownstream_gene_variant
UCEC-US157857242578572425single base substitutionGAdownstream_gene_variant
UCEC-US157857242578572425single base substitutionGAintron_variant
UCEC-US157857767978577679single base substitutionGAdownstream_gene_variant
UCEC-US157857767978577679single base substitutionGAexon_variant
UCEC-US157857767978577679single base substitutionGAintron_variant
UCEC-US157857767978577679single base substitutionGAmissense_variantS121L362C>T
UCEC-US157857767978577679single base substitutionGAmissense_variantS158L473C>T
UCEC-US157857767978577679single base substitutionGAmissense_variantS251L752C>T
UCEC-US157857840078578400single base substitutionGAdownstream_gene_variant
UCEC-US157857840078578400single base substitutionGAexon_variant
UCEC-US157857840078578400single base substitutionGAintron_variant
UCEC-US157857840078578400single base substitutionGAsynonymous_variantD114D342C>T
UCEC-US157857840078578400single base substitutionGAsynonymous_variantD151D453C>T
UCEC-US157857840078578400single base substitutionGAsynonymous_variantD244D732C>T
UCEC-US157857840078578400single base substitutionGAupstream_gene_variant
UCEC-US157857844578578445single base substitutionGAdownstream_gene_variant
UCEC-US157857844578578445single base substitutionGAexon_variant
UCEC-US157857844578578445single base substitutionGAintron_variant
UCEC-US157857844578578445single base substitutionGAsynonymous_variantS136S408C>T
UCEC-US157857844578578445single base substitutionGAsynonymous_variantS229S687C>T
UCEC-US157857844578578445single base substitutionGAsynonymous_variantS99S297C>T
UCEC-US157857844578578445single base substitutionGAupstream_gene_variant
UCEC-US157858072378580723single base substitutionGAdownstream_gene_variant
UCEC-US157858072378580723single base substitutionGAsplice_region_variant
UCEC-US157858072378580723single base substitutionGAupstream_gene_variant
UCEC-US157858230778582307single base substitutionGT3_prime_UTR_variant
UCEC-US157858230778582307single base substitutionGTdownstream_gene_variant
UCEC-US157858230778582307single base substitutionGTexon_variant
UCEC-US157858230778582307single base substitutionGTmissense_variantL152I454C>A
UCEC-US157858230778582307single base substitutionGTmissense_variantL22I64C>A
UCEC-US157858230778582307single base substitutionGTmissense_variantL59I175C>A
UCEC-US157858230778582307single base substitutionGTupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
I2L-P24Ta-Tumor-BiopsyCOSM5363008c.257C>Tp.A86VSubstitution - Missense15:78292678-78292678-
ESCC_BICR_008TCOSM5428827c.505G>Ap.D169NSubstitution - Missense15:78289676-78289676-
I2L-P24Tb-Tumor-BiopsyCOSM5363008c.257C>Tp.A86VSubstitution - Missense15:78292678-78292678-
TCGA-B5-A0JY-01COSM965350c.454C>Ap.L152ISubstitution - Missense15:78289965-78289965-
YUKATCOSM5383876c.816T>Ap.D272ESubstitution - Missense15:78285273-78285273-
TCGA-AA-3697-01COSM1374775c.211G>Tp.D71YSubstitution - Missense15:78292724-78292724-
LIM1899COSM4640025c.595T>Cp.S199PSubstitution - Missense15:78288350-78288350-
TCGA-BR-6452-01COSM4057131c.510A>Gp.G170GSubstitution - coding silent15:78289671-78289671-
TCGA-BR-6452-01COSM4057132c.478G>Tp.G160WSubstitution - Missense15:78289703-78289703-
RK052_C01COSM1629696c.430T>Cp.L144LSubstitution - coding silent15:78289989-78289989-
HDC87COSM4636936c.480G>Tp.G160GSubstitution - coding silent15:78289701-78289701-
PD13755aCOSM5777087c.513C>Ap.I171ISubstitution - coding silent15:78289668-78289668-
S00827COSM316544c.822_823GG>ATp.Q274>?Complex15:78285266-78285267-
KM12COSM2011048c.554C>Gp.T185SSubstitution - Missense15:78289627-78289627-
S00827COSM316544c.822_823GG>ATp.Q274>?Complex15:78285266-78285267-
QGP1COSM2011051c.293A>Gp.Q98RSubstitution - Missense15:78292642-78292642-
24TCOSM109469c.243C>Tp.S81SSubstitution - coding silent15:78292692-78292692-
TCGA-B5-A11E-01COSM965347c.732C>Tp.D244DSubstitution - coding silent15:78286058-78286058-
sysucc-1171TCOSM4254353c.657-10C>Tp.?Unknown15:78286143-78286143-
TCGA-AA-A00N-01COSM278127c.752C>Tp.S251LSubstitution - Missense15:78285337-78285337-
TCGA-D8-A27G-01COSM3816824c.156G>Cp.E52DSubstitution - Missense15:78292779-78292779-
TCGA-06-5858-01COSM3401943c.712G>Ap.V238ISubstitution - Missense15:78286078-78286078-
ESCC_76COSM5635101c.132G>Ap.V44VSubstitution - coding silent15:78293181-78293181-
2_PRE-TREATMENTCOSM1722947c.147-10C>Tp.?Unknown15:78292798-78292798-
TCGA-AP-A059-01COSM965349c.564C>Tp.G188GSubstitution - coding silent15:78288381-78288381-
BZ20COSM5758541c.695C>Tp.A232VSubstitution - Missense15:78286095-78286095-
Pat_59_ACOSM5849854c.469-1G>Ap.?Unknown15:78289713-78289713-
ESCC_109COSM5638893c.789G>Ap.T263TSubstitution - coding silent15:78285300-78285300-
046TCOSM1729738c.51T>Ap.D17ESubstitution - Missense15:78293262-78293262-
CSCC-49-TCOSM4449756c.319+1G>Ap.?Unknown15:78292615-78292615-
CSCC-35-TCOSM4495300c.450C>Tp.F150FSubstitution - coding silent15:78289969-78289969-
T2940COSM4741018c.476A>Gp.D159GSubstitution - Missense15:78289705-78289705-
TCGA-AM-5820-01COSM3690556c.364G>Ap.A122TSubstitution - Missense15:78290055-78290055-
I2L-P24Tb-Tumor-OrganoidCOSM5363008c.257C>Tp.A86VSubstitution - Missense15:78292678-78292678-
TCGA-D1-A17Q-01COSM278127c.752C>Tp.S251LSubstitution - Missense15:78285337-78285337-
TC71COSM4578529c.580C>Tp.R194CSubstitution - Missense15:78288365-78288365-
SE3COSM1165813c.797G>Cp.C266SSubstitution - Missense15:78285292-78285292-
TCGA-CM-6162-01COSM1374772c.599C>Tp.P200LSubstitution - Missense15:78288346-78288346-
TCGA-13-0755-01COSM77012c.544C>Tp.L182FSubstitution - Missense15:78289637-78289637-
TCGA-EE-A2MH-06COSM3504294c.606C>Tp.S202SSubstitution - coding silent15:78288339-78288339-
I2L-P24Ta-Tumor-OrganoidCOSM5363008c.257C>Tp.A86VSubstitution - Missense15:78292678-78292678-
TCGA-CM-4746-01COSM1374773c.569C>Tp.A190VSubstitution - Missense15:78288376-78288376-
TCGA-IR-A3LK-01COSM4816536c.820C>Tp.Q274*Substitution - Nonsense15:78285269-78285269-
PT08_2COSM5893857c.698C>Tp.S233FSubstitution - Missense15:78286092-78286092-
CLL125COSM1290435c.511A>Gp.I171VSubstitution - Missense15:78289670-78289670-
PD13755aCOSM5794729c.512T>Ap.I171NSubstitution - Missense15:78289669-78289669-
TCGA-BS-A0U8-01COSM965348c.687C>Tp.S229SSubstitution - coding silent15:78286103-78286103-
PT08_1COSM5893857c.698C>Tp.S233FSubstitution - Missense15:78286092-78286092-
2_RESISTANTCOSM1722947c.147-10C>Tp.?Unknown15:78292798-78292798-
OLID13COSM132786c.568G>Ap.A190TSubstitution - Missense15:78288377-78288377-
T44COSM5342634c.776G>Ap.W259*Substitution - Nonsense15:78285313-78285313-
TCGA-61-1895-01COSM1323819c.829-1G>Ap.?Unknown15:78283522-78283522-
PT21_2COSM5901928c.370G>Ap.G124RSubstitution - Missense15:78290049-78290049-
TCGA-GM-A2DD-01COSM5232540c.576delCp.I193fs*4Deletion - Frameshift15:78288369-78288369-
BD117TCOSM5507426c.398T>Cp.F133SSubstitution - Missense15:78290021-78290021-
sysucc-923TCOSM4254353c.657-10C>Tp.?Unknown15:78286143-78286143-
YUOTHOCOSM5383877c.344C>Tp.S115FSubstitution - Missense15:78290075-78290075-
TCGA-AA-3697-01COSM1374776c.210G>Tp.V70VSubstitution - coding silent15:78292725-78292725-
RK217_C01COSM3741685c.367A>Gp.T123ASubstitution - Missense15:78290052-78290052-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.51305515q25.1609540
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGIntronicSNV.c.1-50T>C1578588078RCCC
ATIntronicSNV.c.320-567T>A1578583008HC
CAIntronicSNV.c.41-16G>T1578585630MB
CASpliceDonorSNV.c.319+1G>T1578584957LUAD
CCATMissensep.D275Yc.822_823delinsAT1578577608SCLC
CGIntronicSNV.c.12+63G>C1578587954HC
GAIntronicSNV.c.1-99C>T1578588127CM
GAIntronicSNV.c.40+53C>T1578587235CM
GAMissensep.L182Fc.544C>T1578581979OV
GASynonymousp.S202Sc.606C>T1578580681CM
GASynonymousp.S229Sc.687C>T1578578445UCEC
TCMissensep.I171Vc.511A>G1578582012CLL