NEDD8
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA142468637724686377+Missense_MutationSNPGGATCGA-K4-A6FZ-01A-11D-A31L-08TCGA-K4-A6FZ-10A-01D-A31J-08g.chr14:24686377G>Ac.202C>Tc.(202-204)Cac>Tacp.H68Y
BLCA142468735624687356+SilentSNPGGATCGA-H4-A2HQ-01A-11D-A17V-08TCGA-H4-A2HQ-10A-01D-A17V-08g.chr14:24687356G>Ac.132C>Tc.(130-132)atC>atTp.I44I
BLCA142468762224687622+Missense_MutationSNPCCTTCGA-UY-A8OB-01A-12D-A42E-08TCGA-UY-A8OB-11A-12D-A42H-08g.chr14:24687622C>Tc.34G>Ac.(34-36)Gag>Aagp.E12K
BRCA142468741024687410+Missense_MutationSNPGGCTCGA-A2-A0YK-01A-22D-A117-09TCGA-A2-A0YK-10A-01D-A117-09g.chr14:24687410G>Cc.78C>Gc.(76-78)atC>atGp.I26M
COADREAD142468741424687414+Missense_MutationSNPCCTTCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr14:24687414C>Tc.74G>Ac.(73-75)cGa>cAap.R25Q
ESCA142468640324686403+Missense_MutationSNPTTATCGA-LN-A9FP-01A-31D-A387-09TCGA-LN-A9FP-10A-01D-A38A-09g.chr14:24686403T>Ac.176A>Tc.(175-177)tAc>tTcp.Y59F
ESCA142468734224687342+Missense_MutationSNPTTCTCGA-LN-A49U-01A-31D-A27G-09TCGA-LN-A49U-10A-01D-A27G-09g.chr14:24687342T>Cc.146A>Gc.(145-147)cAg>cGgp.Q49R
GBMLGG142468763424687634+SilentSNPGGATCGA-RY-A840-01A-11D-A36O-08TCGA-RY-A840-10A-01D-A367-08g.chr14:24687634G>Ac.22C>Tc.(22-24)Ctg>Ttgp.L8L
HNSC142468641524686415+Missense_MutationSNPGGCTCGA-DQ-5625-01A-01D-1870-08TCGA-DQ-5625-10A-01D-1870-08g.chr14:24686415G>Cc.164C>Gc.(163-165)aCa>aGap.T55R
HNSC142468763624687636+Splice_SiteSNPGGATCGA-UF-A719-01A-12D-A34J-08TCGA-UF-A719-10A-01D-A34M-08g.chr14:24687636G>Ac.20C>Tc.(19-21)aCg>aTgp.T7M
LGG142468763424687634+SilentSNPGGATCGA-RY-A840-01A-11D-A36O-08TCGA-RY-A840-10A-01D-A367-08g.chr14:24687634G>Ac.22C>Tc.(22-24)Ctg>Ttgp.L8L
LUAD142468741424687414+Missense_MutationSNPCCTTCGA-05-4403-01A-01D-1265-08TCGA-05-4403-10A-01D-1265-08g.chr14:24687414C>Tc.74G>Ac.(73-75)cGa>cAap.R25Q
LUAD142468742124687421+Splice_SiteSNPCCTTCGA-05-4433-01A-22D-1855-08TCGA-05-4433-10A-01D-1855-08g.chr14:24687421C>Tc.67G>Ac.(67-69)Gtg>Atgp.V23M
READ142468741424687414+Missense_MutationSNPCCTTCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr14:24687414C>Tc.74G>Ac.(73-75)cGa>cAap.R25Q
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN142468272224682722single base substitutionACdownstream_gene_variant
BLCA-CN142468475924684759single base substitutionTGdownstream_gene_variant
BLCA-CN142470253924702539single base substitutionGAupstream_gene_variant
BLCA-US142468735624687356single base substitutionGAexon_variant
BLCA-US142468735624687356single base substitutionGAintron_variant
BLCA-US142468735624687356single base substitutionGAsynonymous_variantI44I132C>T
BRCA-EU142468217824682178single base substitutionGCdownstream_gene_variant
BRCA-EU142468261924682619single base substitutionCTdownstream_gene_variant
BRCA-EU142468283224682832single base substitutionGTdownstream_gene_variant
BRCA-EU142468322124683221single base substitutionCTdownstream_gene_variant
BRCA-EU142468522424685224single base substitutionGAdownstream_gene_variant
BRCA-EU142468565124685651single base substitutionGCdownstream_gene_variant
BRCA-EU142468577924685779single base substitutionGAdownstream_gene_variant
BRCA-EU142468737524687375insertion of <=200bp-Gexon_variant
BRCA-EU142468737524687375insertion of <=200bp-Gframeshift_variantP38P?
BRCA-EU142468737524687375insertion of <=200bp-Gintron_variant
BRCA-EU142468840524688405single base substitutionCTintron_variant
BRCA-EU142468840524688405single base substitutionCTupstream_gene_variant
BRCA-EU142469207324692073single base substitutionCTdownstream_gene_variant
BRCA-EU142469207324692073single base substitutionCTintron_variant
BRCA-EU142469207324692073single base substitutionCTupstream_gene_variant
BRCA-EU142469260624692606deletion of <=200bpA-downstream_gene_variant
BRCA-EU142469260624692606deletion of <=200bpA-intron_variant
BRCA-EU142469260624692606deletion of <=200bpA-upstream_gene_variant
BRCA-EU142469329424693294single base substitutionCGdownstream_gene_variant
BRCA-EU142469329424693294single base substitutionCGintron_variant
BRCA-EU142469459424694594single base substitutionGAdownstream_gene_variant
BRCA-EU142469459424694594single base substitutionGAintron_variant
BRCA-EU142469732524697325single base substitutionCTexon_variant
BRCA-EU142469732524697325single base substitutionCTintron_variant
BRCA-EU142469777324697773single base substitutionTCexon_variant
BRCA-EU142469777324697773single base substitutionTCintron_variant
BRCA-EU142469852424698524single base substitutionCGintron_variant
BRCA-EU142469919024699190single base substitutionCTintron_variant
BRCA-EU142470061324700616deletion of <=200bpAAAT-intron_variant
BRCA-EU142470087124700871deletion of <=200bpG-exon_variant
BRCA-EU142470087124700871deletion of <=200bpG-intron_variant
BRCA-EU142470126724701267single base substitutionGAintron_variant
BRCA-EU142470126724701267single base substitutionGAupstream_gene_variant
BRCA-EU142470160524701605single base substitutionCT5_prime_UTR_variant
BRCA-EU142470160524701605single base substitutionCTupstream_gene_variant
BRCA-EU142470175224701752single base substitutionGCupstream_gene_variant
BRCA-EU142470435924704359single base substitutionGAupstream_gene_variant
BRCA-EU142470479924704799single base substitutionCGupstream_gene_variant
BRCA-EU142470484624704846single base substitutionTGupstream_gene_variant
BRCA-FR142468322124683221single base substitutionCTdownstream_gene_variant
BRCA-FR142468373424683734single base substitutionTGdownstream_gene_variant
BRCA-FR142468522424685224single base substitutionGAdownstream_gene_variant
BRCA-FR142468577924685779single base substitutionGAdownstream_gene_variant
BRCA-FR142469207324692073single base substitutionCTdownstream_gene_variant
BRCA-FR142469207324692073single base substitutionCTintron_variant
BRCA-FR142469207324692073single base substitutionCTupstream_gene_variant
BRCA-FR142469459424694594single base substitutionGAdownstream_gene_variant
BRCA-FR142469459424694594single base substitutionGAintron_variant
BRCA-FR142469685124696851single base substitutionGAexon_variant
BRCA-FR142469685124696851single base substitutionGAintron_variant
BRCA-FR142469852424698524single base substitutionCGintron_variant
BRCA-FR142470126724701267single base substitutionGAintron_variant
BRCA-FR142470126724701267single base substitutionGAupstream_gene_variant
BRCA-FR142470435924704359single base substitutionGAupstream_gene_variant
BRCA-UK142468513524685135single base substitutionGAdownstream_gene_variant
BRCA-UK142469251124692511single base substitutionGAdownstream_gene_variant
BRCA-UK142469251124692511single base substitutionGAintron_variant
BRCA-UK142469251124692511single base substitutionGAupstream_gene_variant
BRCA-US142468334024683340single base substitutionTCdownstream_gene_variant
BRCA-US142468376424683764single base substitutionACdownstream_gene_variant
BRCA-US142468486724684867single base substitutionCTdownstream_gene_variant
BRCA-US142468741024687410single base substitutionGCexon_variant
BRCA-US142468741024687410single base substitutionGCintron_variant
BRCA-US142468741024687410single base substitutionGCmissense_variantI26M78C>G
BRCA-US142470244524702445single base substitutionCTupstream_gene_variant
BTCA-JP142468342724683433deletion of <=200bpTGCCACC-downstream_gene_variant
BTCA-JP142468645024686450deletion of <=200bpA-downstream_gene_variant
BTCA-JP142468645024686450deletion of <=200bpA-intron_variant
BTCA-JP142468651024686510single base substitutionGTdownstream_gene_variant
BTCA-JP142468651024686510single base substitutionGTintron_variant
BTCA-JP142470283224702832single base substitutionAGupstream_gene_variant
CESC-US142468354924683549single base substitutionCGdownstream_gene_variant
CESC-US142468498424684984single base substitutionGAdownstream_gene_variant
CLLE-ES142469808824698088single base substitutionCGintron_variant
COAD-US142468499624684996single base substitutionACdownstream_gene_variant
COCA-CN142468513124685131single base substitutionCAdownstream_gene_variant
COCA-CN142468642024686420single base substitutionCA3_prime_UTR_variant
COCA-CN142468642024686420single base substitutionCAdownstream_gene_variant
COCA-CN142468642024686420single base substitutionCAexon_variant
COCA-CN142468642024686420single base substitutionCAmissense_variantE53D159G>T
COCA-CN142468760424687604single base substitutionCGexon_variant
COCA-CN142468760424687604single base substitutionCGintron_variant
COCA-CN142468760424687604single base substitutionCGmissense_variantE18Q52G>C
COCA-CN142470297924702979single base substitutionCGupstream_gene_variant
COCA-CN142470327024703270single base substitutionGTupstream_gene_variant
COCA-CN142470503424705034single base substitutionTGupstream_gene_variant
COCA-CN142470617424706174single base substitutionCAupstream_gene_variant
COCA-CN142470650424706504single base substitutionGAupstream_gene_variant
ESAD-UK142468215924682159single base substitutionGTdownstream_gene_variant
ESAD-UK142468230124682301single base substitutionCGdownstream_gene_variant
ESAD-UK142468241224682412single base substitutionGAdownstream_gene_variant
ESAD-UK142468826524688265single base substitutionATintron_variant
ESAD-UK142468826524688265single base substitutionATupstream_gene_variant
ESAD-UK142469145224691452deletion of <=200bpA-downstream_gene_variant
ESAD-UK142469145224691452deletion of <=200bpA-intron_variant
ESAD-UK142469145224691452deletion of <=200bpA-upstream_gene_variant
ESAD-UK142469152324691523single base substitutionTCdownstream_gene_variant
ESAD-UK142469152324691523single base substitutionTCintron_variant
ESAD-UK142469152324691523single base substitutionTCupstream_gene_variant
ESAD-UK142469388424693884single base substitutionAGdownstream_gene_variant
ESAD-UK142469388424693884single base substitutionAGintron_variant
ESAD-UK142469413124694131single base substitutionGAdownstream_gene_variant
ESAD-UK142469413124694131single base substitutionGAintron_variant
ESAD-UK142469426824694268single base substitutionGAdownstream_gene_variant
ESAD-UK142469426824694268single base substitutionGAintron_variant
ESAD-UK142469667224696672single base substitutionCTexon_variant
ESAD-UK142469667224696672single base substitutionCTintron_variant
ESAD-UK142470050424700504single base substitutionTGintron_variant
ESAD-UK142470083824700838single base substitutionCTintron_variant
ESAD-UK142470662324706623single base substitutionGAupstream_gene_variant
ESCA-CN142468638824686388single base substitutionCG3_prime_UTR_variant
ESCA-CN142468638824686388single base substitutionCGdownstream_gene_variant
ESCA-CN142468638824686388single base substitutionCGexon_variant
ESCA-CN142468638824686388single base substitutionCGmissense_variantG64A191G>C
GBM-US142468335124683351single base substitutionGAdownstream_gene_variant
LAML-KR142468312524683125single base substitutionAGdownstream_gene_variant
LAML-KR142469523124695231single base substitutionTGdownstream_gene_variant
LAML-KR142469523124695231single base substitutionTGintron_variant
LAML-KR142470529524705295single base substitutionTCupstream_gene_variant
LICA-FR142469565224695653deletion of <=200bpAA-downstream_gene_variant
LICA-FR142469565224695653deletion of <=200bpAA-intron_variant
LINC-JP142468751224687512single base substitutionAGintron_variant
LINC-JP142470276624702766insertion of <=200bp-Aupstream_gene_variant
LINC-JP142470337224703372single base substitutionCGupstream_gene_variant
LINC-JP142470377324703773single base substitutionAGupstream_gene_variant
LINC-JP142470435524704355single base substitutionACupstream_gene_variant
LIRI-JP142468129424681294single base substitutionAGdownstream_gene_variant
LIRI-JP142468407324684073single base substitutionCGdownstream_gene_variant
LIRI-JP142468521324685213single base substitutionTCdownstream_gene_variant
LIRI-JP142468787324687873single base substitutionCAexon_variant
LIRI-JP142468787324687873single base substitutionCAintron_variant
LIRI-JP142468899024688990single base substitutionGAintron_variant
LIRI-JP142468899024688990single base substitutionGAupstream_gene_variant
LIRI-JP142469218924692189single base substitutionGTdownstream_gene_variant
LIRI-JP142469218924692189single base substitutionGTintron_variant
LIRI-JP142469218924692189single base substitutionGTupstream_gene_variant
LIRI-JP142469607824696078single base substitutionACexon_variant
LIRI-JP142469607824696078single base substitutionACintron_variant
LIRI-JP142469900824699008single base substitutionGAintron_variant
LIRI-JP142469914924699149single base substitutionCTintron_variant
LIRI-JP142470187124701871single base substitutionATupstream_gene_variant
LIRI-JP142470240124702401single base substitutionTGupstream_gene_variant
LIRI-JP142470593124705931single base substitutionAGupstream_gene_variant
LIRI-JP142470600124706001single base substitutionGAupstream_gene_variant
LUSC-KR142468777124687771single base substitutionGAexon_variant
LUSC-KR142468777124687771single base substitutionGAintron_variant
LUSC-KR142468802324688023single base substitutionGAintron_variant
LUSC-KR142468802324688023single base substitutionGAupstream_gene_variant
LUSC-KR142468924624689246single base substitutionGAintron_variant
LUSC-KR142468924624689246single base substitutionGAupstream_gene_variant
LUSC-KR142469294524692945single base substitutionATdownstream_gene_variant
LUSC-KR142469294524692945single base substitutionATintron_variant
LUSC-KR142469705924697059single base substitutionGTexon_variant
LUSC-KR142469705924697059single base substitutionGTintron_variant
LUSC-KR142470019424700194single base substitutionCTintron_variant
LUSC-KR142470071224700712single base substitutionTGintron_variant
LUSC-US142468481624684816single base substitutionCAdownstream_gene_variant
MALY-DE142468170124681701single base substitutionTAdownstream_gene_variant
MALY-DE142468369524683695single base substitutionTCdownstream_gene_variant
MALY-DE142468475524684755single base substitutionTCdownstream_gene_variant
MALY-DE142469287224692872single base substitutionACdownstream_gene_variant
MALY-DE142469287224692872single base substitutionACintron_variant
MALY-DE142469287224692872single base substitutionACupstream_gene_variant
MALY-DE142469628824696288single base substitutionAGexon_variant
MALY-DE142469628824696288single base substitutionAGintron_variant
MALY-DE142469631124696311single base substitutionTGexon_variant
MALY-DE142469631124696311single base substitutionTGintron_variant
MELA-AU142468256024682560single base substitutionCTdownstream_gene_variant
MELA-AU142468273124682731single base substitutionGAdownstream_gene_variant
MELA-AU142468308224683082single base substitutionCTdownstream_gene_variant
MELA-AU142468498824684989multiple base substitution (>=2bp and <=200bp)GGTAdownstream_gene_variant
MELA-AU142468577624685776single base substitutionGAdownstream_gene_variant
MELA-AU142468617624686176single base substitutionGA3_prime_UTR_variant
MELA-AU142468617624686176single base substitutionGAdownstream_gene_variant
MELA-AU142468617624686176single base substitutionGAexon_variant
MELA-AU142468643524686435single base substitutionGAdownstream_gene_variant
MELA-AU142468643524686435single base substitutionGAintron_variant
MELA-AU142468738024687380single base substitutionGAexon_variant
MELA-AU142468738024687380single base substitutionGAintron_variant
MELA-AU142468738024687380single base substitutionGAsynonymous_variantI36I108C>T
MELA-AU142468747724687477single base substitutionGAintron_variant
MELA-AU142468760024687601multiple base substitution (>=2bp and <=200bp)GGAAexon_variant
MELA-AU142468760024687601multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU142468760024687601multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantP19F55CC>TT
MELA-AU142468797524687976multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU142468797524687976multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU142468823124688231single base substitutionGAintron_variant
MELA-AU142468823124688231single base substitutionGAupstream_gene_variant
MELA-AU142468837424688374single base substitutionAGintron_variant
MELA-AU142468837424688374single base substitutionAGupstream_gene_variant
MELA-AU142468840024688400single base substitutionGAintron_variant
MELA-AU142468840024688400single base substitutionGAupstream_gene_variant
MELA-AU142468959724689597single base substitutionGAintron_variant
MELA-AU142468959724689597single base substitutionGAupstream_gene_variant
MELA-AU142469001424690014single base substitutionGAintron_variant
MELA-AU142469001424690014single base substitutionGAupstream_gene_variant
MELA-AU142469012824690128single base substitutionGAintron_variant
MELA-AU142469012824690128single base substitutionGAupstream_gene_variant
MELA-AU142469031124690311single base substitutionGAintron_variant
MELA-AU142469031124690311single base substitutionGAupstream_gene_variant
MELA-AU142469062824690628single base substitutionGAintron_variant
MELA-AU142469062824690628single base substitutionGAupstream_gene_variant
MELA-AU142469083524690835single base substitutionCTdownstream_gene_variant
MELA-AU142469083524690835single base substitutionCTintron_variant
MELA-AU142469083524690835single base substitutionCTupstream_gene_variant
MELA-AU142469096524690965single base substitutionGAdownstream_gene_variant
MELA-AU142469096524690965single base substitutionGAintron_variant
MELA-AU142469096524690965single base substitutionGAupstream_gene_variant
MELA-AU142469111524691115single base substitutionGAdownstream_gene_variant
MELA-AU142469111524691115single base substitutionGAintron_variant
MELA-AU142469111524691115single base substitutionGAupstream_gene_variant
MELA-AU142469247624692476single base substitutionGAdownstream_gene_variant
MELA-AU142469247624692476single base substitutionGAintron_variant
MELA-AU142469247624692476single base substitutionGAupstream_gene_variant
MELA-AU142469258824692588single base substitutionGAdownstream_gene_variant
MELA-AU142469258824692588single base substitutionGAintron_variant
MELA-AU142469258824692588single base substitutionGAupstream_gene_variant
MELA-AU142469259024692590single base substitutionGAdownstream_gene_variant
MELA-AU142469259024692590single base substitutionGAintron_variant
MELA-AU142469259024692590single base substitutionGAupstream_gene_variant
MELA-AU142469274624692746single base substitutionTCdownstream_gene_variant
MELA-AU142469274624692746single base substitutionTCintron_variant
MELA-AU142469274624692746single base substitutionTCupstream_gene_variant
MELA-AU142469298424692984single base substitutionCTdownstream_gene_variant
MELA-AU142469298424692984single base substitutionCTintron_variant
MELA-AU142469318224693182single base substitutionGAdownstream_gene_variant
MELA-AU142469318224693182single base substitutionGAintron_variant
MELA-AU142469376124693761single base substitutionCTdownstream_gene_variant
MELA-AU142469376124693761single base substitutionCTintron_variant
MELA-AU142469471424694714single base substitutionGAdownstream_gene_variant
MELA-AU142469471424694714single base substitutionGAintron_variant
MELA-AU142469516124695161single base substitutionCAdownstream_gene_variant
MELA-AU142469516124695161single base substitutionCAintron_variant
MELA-AU142469516324695163single base substitutionTAdownstream_gene_variant
MELA-AU142469516324695163single base substitutionTAintron_variant
MELA-AU142469611624696116single base substitutionACexon_variant
MELA-AU142469611624696116single base substitutionACintron_variant
MELA-AU142469615624696156single base substitutionGAexon_variant
MELA-AU142469615624696156single base substitutionGAintron_variant
MELA-AU142469652924696529single base substitutionGAexon_variant
MELA-AU142469652924696529single base substitutionGAintron_variant
MELA-AU142469663024696630single base substitutionGAexon_variant
MELA-AU142469663024696630single base substitutionGAintron_variant
MELA-AU142469799324697993single base substitutionTCintron_variant
MELA-AU142469886024698860single base substitutionGAintron_variant
MELA-AU142469887124698871single base substitutionAGintron_variant
MELA-AU142469998624699986single base substitutionGAintron_variant
MELA-AU142470157824701578single base substitutionCT5_prime_UTR_variant
MELA-AU142470157824701578single base substitutionCTupstream_gene_variant
MELA-AU142470441924704419single base substitutionGAupstream_gene_variant
MELA-AU142470616924706170multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
OV-AU142468157624681576single base substitutionCGdownstream_gene_variant
OV-AU142468492124684921single base substitutionGTdownstream_gene_variant
OV-AU142468553724685537single base substitutionTCdownstream_gene_variant
OV-AU142469426424694264single base substitutionCGdownstream_gene_variant
OV-AU142469426424694264single base substitutionCGintron_variant
OV-AU142469526424695264single base substitutionACdownstream_gene_variant
OV-AU142469526424695264single base substitutionACintron_variant
OV-AU142470302224703022single base substitutionTGupstream_gene_variant
PACA-AU142468181724681817single base substitutionTCdownstream_gene_variant
PACA-AU142468447524684475single base substitutionAGdownstream_gene_variant
PACA-AU142469422724694227single base substitutionTCdownstream_gene_variant
PACA-AU142469422724694227single base substitutionTCintron_variant
PACA-AU142469669824696698single base substitutionGAexon_variant
PACA-AU142469669824696698single base substitutionGAintron_variant
PACA-AU142469918424699184single base substitutionGAintron_variant
PACA-AU142469952224699522single base substitutionCTintron_variant
PACA-CA142468841024688410single base substitutionGAintron_variant
PACA-CA142468841024688410single base substitutionGAupstream_gene_variant
PACA-CA142469274924692749single base substitutionATdownstream_gene_variant
PACA-CA142469274924692749single base substitutionATintron_variant
PACA-CA142469274924692749single base substitutionATupstream_gene_variant
PACA-CA142470486124704861single base substitutionCGupstream_gene_variant
PACA-CA142470486424704864single base substitutionACupstream_gene_variant
PACA-CA142470493724704937single base substitutionCGupstream_gene_variant
PACA-CA142470555324705553single base substitutionTCupstream_gene_variant
PAEN-AU142469563724695637single base substitutionGCdownstream_gene_variant
PAEN-AU142469563724695637single base substitutionGCintron_variant
PBCA-DE142468740324687403single base substitutionGAexon_variant
PBCA-DE142468740324687403single base substitutionGAintron_variant
PBCA-DE142468740324687403single base substitutionGAmissense_variantR29C85C>T
PBCA-DE142469671124696711single base substitutionGCexon_variant
PBCA-DE142469671124696711single base substitutionGCintron_variant
PRAD-CA142469364324693643single base substitutionCGdownstream_gene_variant
PRAD-CA142469364324693643single base substitutionCGintron_variant
PRAD-UK142468665224686652single base substitutionCTdownstream_gene_variant
PRAD-UK142468665224686652single base substitutionCTintron_variant
PRAD-US142468265224682652single base substitutionCGdownstream_gene_variant
PRAD-US142470273224702732single base substitutionCAupstream_gene_variant
READ-US142468328724683287single base substitutionCTdownstream_gene_variant
READ-US142468374124683741single base substitutionGTdownstream_gene_variant
READ-US142470635024706350single base substitutionTGupstream_gene_variant
RECA-EU142468270524682705single base substitutionTAdownstream_gene_variant
RECA-EU142468565524685655single base substitutionGAdownstream_gene_variant
RECA-EU142469810924698109single base substitutionATintron_variant
SKCA-BR142468148624681486single base substitutionACdownstream_gene_variant
SKCA-BR142468175524681755single base substitutionACdownstream_gene_variant
SKCA-BR142468263624682636single base substitutionGCdownstream_gene_variant
SKCA-BR142468463824684638single base substitutionGAdownstream_gene_variant
SKCA-BR142468643624686436single base substitutionGAdownstream_gene_variant
SKCA-BR142468643624686436single base substitutionGAintron_variant
SKCA-BR142468745724687457single base substitutionGAintron_variant
SKCA-BR142469293224692932insertion of <=200bp-GAdownstream_gene_variant
SKCA-BR142469293224692932insertion of <=200bp-GAintron_variant
SKCA-BR142469293224692932insertion of <=200bp-GAupstream_gene_variant
SKCA-BR142469351324693513single base substitutionACdownstream_gene_variant
SKCA-BR142469351324693513single base substitutionACintron_variant
SKCA-BR142469437724694377insertion of <=200bp-CAdownstream_gene_variant
SKCA-BR142469437724694377insertion of <=200bp-CAintron_variant
SKCA-BR142470245324702453single base substitutionAGupstream_gene_variant
SKCM-US142468266924682669single base substitutionCAdownstream_gene_variant
SKCM-US142468268824682688single base substitutionGAdownstream_gene_variant
SKCM-US142468486324684863single base substitutionCTdownstream_gene_variant
SKCM-US142470157824701578single base substitutionCT5_prime_UTR_variant
SKCM-US142470157824701578single base substitutionCTupstream_gene_variant
SKCM-US142470633924706339single base substitutionCTupstream_gene_variant
STAD-US142470533424705334single base substitutionGAupstream_gene_variant
UCEC-US142468324024683240single base substitutionACdownstream_gene_variant
UCEC-US142468325724683257single base substitutionGAdownstream_gene_variant
UCEC-US142468330924683309single base substitutionCTdownstream_gene_variant
UCEC-US142468636024686360single base substitutionCG3_prime_UTR_variant
UCEC-US142468636024686360single base substitutionCGdownstream_gene_variant
UCEC-US142468636024686360single base substitutionCGexon_variant
UCEC-US142468636024686360single base substitutionCGsynonymous_variantL73L219G>C
UCEC-US142470277424702774single base substitutionCTupstream_gene_variant
UCEC-US142470498924704989single base substitutionGCupstream_gene_variant
UCEC-US142470654224706542single base substitutionATupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-AG-3892-01COSM257509c.74G>Ap.R25QSubstitution - Missense14:24218208-24218208-
PAPNNXCOSM5005035c.86G>Ap.R29HSubstitution - Missense14:24218196-24218196-
MD-319COSM302738c.85C>Tp.R29CSubstitution - Missense14:24218197-24218197-
61COSM5005035c.86G>Ap.R29HSubstitution - Missense14:24218196-24218196-
229COSM2032922c.131T>Cp.I44TSubstitution - Missense14:24218151-24218151-
HCT116COSM2032922c.131T>Cp.I44TSubstitution - Missense14:24218151-24218151-
LC_S45COSM1188784c.222A>Tp.R74SSubstitution - Missense14:24217151-24217151-
ESCC-128TCOSM3936489c.191G>Cp.G64ASubstitution - Missense14:24217182-24217182-
TCGA-H4-A2HQ-01COSM1300538c.132C>Tp.I44ISubstitution - coding silent14:24218150-24218150-
TCGA-A2-A0YK-01COSM432947c.78C>Gp.I26MSubstitution - Missense14:24218204-24218204-
TCGA-B5-A11R-01COSM954966c.219G>Cp.L73LSubstitution - coding silent14:24217154-24217154-
ICGC_MB126COSM302738c.85C>Tp.R29CSubstitution - Missense14:24218197-24218197-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.531042;Hs.531053;Hs.53106414q12603171
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
CANonsensep.G76*c.226G>T1424686353STAD
CT5-UTRSNV.c.1-105G>A1424701578CM
CTMissensep.R25Qc.74G>A1424687414LUAD
CTMissensep.V23Mc.67G>A1424687421LUAD
GAMissensep.P37Sc.109C>T1424687379CM
GAMissensep.R29Cc.85C>T1424687403MB
GCMissensep.I26Mc.78C>G1424687410BRCA
GCMissensep.T55Rc.164C>G1424686415HNSC