KCTD5
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA1627523702752370+Missense_MutationSNPCCATCGA-FD-A5BT-01A-11D-A26M-08TCGA-FD-A5BT-10A-01D-A26K-08g.chr16:2752370C>Ac.566C>Ac.(565-567)tCc>tAcp.S189Y
BRCA1627459592745959+SilentSNPCCTTCGA-OL-A5RX-01A-11D-A28B-09TCGA-OL-A5RX-10A-01D-A28E-09g.chr16:2745959C>Tc.276C>Tc.(274-276)atC>atTp.I92I
COAD1627327042732704+Missense_MutationSNPGGATCGA-A6-6648-01A-11D-1771-10TCGA-A6-6648-10A-01D-1771-10g.chr16:2732704G>Ac.155G>Ac.(154-156)gGc>gAcp.G52D
COAD1627499012749901+Missense_MutationSNPGGATCGA-AA-3492-01A-01D-1408-10TCGA-AA-3492-11A-01D-1408-10g.chr16:2749901G>Ac.533G>Ac.(532-534)gGc>gAcp.G178D
COADREAD1627327042732704+Missense_MutationSNPGGATCGA-A6-6648-01A-11D-1771-10TCGA-A6-6648-10A-01D-1771-10g.chr16:2732704G>Ac.155G>Ac.(154-156)gGc>gAcp.G52D
COADREAD1627499012749901+Missense_MutationSNPGGATCGA-AA-3492-01A-01D-1408-10TCGA-AA-3492-11A-01D-1408-10g.chr16:2749901G>Ac.533G>Ac.(532-534)gGc>gAcp.G178D
ESCA1627499012749901+Missense_MutationSNPGGATCGA-L5-A8NV-01A-11D-A37C-09TCGA-L5-A8NV-11A-11D-A37F-09g.chr16:2749901G>Ac.533G>Ac.(532-534)gGc>gAcp.G178D
ESCA1627524462752446+SilentSNPCCTTCGA-JY-A6FB-01A-11D-A33E-09TCGA-JY-A6FB-10A-01D-A33H-09g.chr16:2752446C>Tc.642C>Tc.(640-642)taC>taTp.Y214Y
GBMLGG1627479852747985+Missense_MutationSNPGGATCGA-QH-A65X-01A-11D-A32B-08TCGA-QH-A65X-10D-01D-A329-08g.chr16:2747985G>Ac.440G>Ac.(439-441)aGc>aAcp.S147N
LGG1627479852747985+Missense_MutationSNPGGATCGA-QH-A65X-01A-11D-A32B-08TCGA-QH-A65X-10D-01D-A329-08g.chr16:2747985G>Ac.440G>Ac.(439-441)aGc>aAcp.S147N
LUAD1627327242732724+Missense_MutationSNPCCGTCGA-71-8520-01A-11D-2393-08TCGA-71-8520-10A-01D-2393-08g.chr16:2732724C>Gc.175C>Gc.(175-177)Cgg>Gggp.R59G
LUAD1627498792749879+Missense_MutationSNPAATTCGA-75-6214-01A-41D-1945-08TCGA-75-6214-10A-01D-1946-08g.chr16:2749879A>Tc.511A>Tc.(511-513)Atg>Ttgp.M171L
LUAD1627524072752408+Frame_Shift_DelDELCCCC-TCGA-49-6743-01A-11D-1855-08TCGA-49-6743-11A-01D-1855-08g.chr16:2752407_2752408delCCc.603_604delCCc.(601-606)ttcctcfsp.L202fs
LUAD1627524312752431+SilentSNPGGTTCGA-95-7947-01A-11D-2184-08TCGA-95-7947-10A-01D-2184-08g.chr16:2752431G>Tc.627G>Tc.(625-627)ctG>ctTp.L209L
LUSC1627498422749842+SilentSNPCCTTCGA-66-2756-01A-01D-1522-08TCGA-66-2756-11A-01D-1522-08g.chr16:2749842C>Tc.474C>Tc.(472-474)taC>taTp.Y158Y
PCPG1627327472732747+SilentSNPGGATCGA-SP-A6QK-01A-11D-A35I-08TCGA-SP-A6QK-10A-01D-A35G-08g.chr16:2732747G>Ac.198G>Ac.(196-198)ccG>ccAp.P66P
PRAD1627524522752452+SilentSNPGGATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr16:2752452G>Ac.648G>Ac.(646-648)acG>acAp.T216T
SKCM1627326872732687+SilentSNPCCTTCGA-FS-A1ZZ-06A-11D-A197-08TCGA-FS-A1ZZ-10A-01D-A199-08g.chr16:2732687C>Tc.138C>Tc.(136-138)gtC>gtTp.V46V
SKCM1627327532732753+SilentSNPCCTTCGA-GN-A265-06A-21D-A197-08TCGA-GN-A265-10A-01D-A199-08g.chr16:2732753C>Tc.204C>Tc.(202-204)tcC>tcTp.S68S
SKCM1627479942747994+Missense_MutationSNPCCTTCGA-D3-A2JP-06A-11D-A19A-08TCGA-D3-A2JP-10A-01D-A19A-08g.chr16:2747994C>Tc.449C>Tc.(448-450)tCg>tTgp.S150L
SKCM1627498292749829+Missense_MutationSNPTTGTCGA-FS-A1ZK-06A-11D-A197-08TCGA-FS-A1ZK-10A-01D-A199-08g.chr16:2749829T>Gc.461T>Gc.(460-462)gTg>gGgp.V154G
SKCM1627573142757314+Missense_MutationSNPGGATCGA-EE-A3J5-06A-11D-A20D-08TCGA-EE-A3J5-10A-01D-A20D-08g.chr16:2757314G>Ac.691G>Ac.(691-693)Ggc>Agcp.G231S
SKCM1627573182757318+Missense_MutationSNPCCTTCGA-EE-A2MF-06A-11D-A21A-08TCGA-EE-A2MF-10B-01D-A21A-08g.chr16:2757318C>Tc.695C>Tc.(694-696)tCa>tTap.S232L
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BRCA-EU1627275932727593single base substitutionGAupstream_gene_variant
BRCA-EU1627284602728460single base substitutionCTupstream_gene_variant
BRCA-EU1627296222729644deletion of <=200bpCTCAGTTCCAGTAGCAGAACCAC-upstream_gene_variant
BRCA-EU1627298722729872single base substitutionGAupstream_gene_variant
BRCA-EU1627301192730119single base substitutionCAupstream_gene_variant
BRCA-EU1627302252730225single base substitutionTCupstream_gene_variant
BRCA-EU1627302332730233single base substitutionTAupstream_gene_variant
BRCA-EU1627306662730666single base substitutionGCupstream_gene_variant
BRCA-EU1627324392732439single base substitutionGTupstream_gene_variant
BRCA-EU1627324822732482single base substitutionCG5_prime_UTR_variant
BRCA-EU1627324822732482single base substitutionCGupstream_gene_variant
BRCA-EU1627324912732491single base substitutionCG5_prime_UTR_variant
BRCA-EU1627324912732491single base substitutionCGupstream_gene_variant
BRCA-EU1627336322733632single base substitutionGTintron_variant
BRCA-EU1627336322733632single base substitutionGTupstream_gene_variant
BRCA-EU1627340262734026single base substitutionCGintron_variant
BRCA-EU1627340262734026single base substitutionCGupstream_gene_variant
BRCA-EU1627356762735676deletion of <=200bpG-exon_variant
BRCA-EU1627356762735676deletion of <=200bpG-intron_variant
BRCA-EU1627358672735867single base substitutionGAexon_variant
BRCA-EU1627358672735867single base substitutionGAintron_variant
BRCA-EU1627367602736760single base substitutionGCintron_variant
BRCA-EU1627368592736859single base substitutionGCintron_variant
BRCA-EU1627382282738229deletion of <=200bpAA-intron_variant
BRCA-EU1627397102739710single base substitutionCTintron_variant
BRCA-EU1627406642740664single base substitutionGAintron_variant
BRCA-EU1627415312741531single base substitutionCTintron_variant
BRCA-EU1627419542741954single base substitutionCGintron_variant
BRCA-EU1627420192742019single base substitutionCGintron_variant
BRCA-EU1627422002742200single base substitutionAGintron_variant
BRCA-EU1627423232742323single base substitutionGAintron_variant
BRCA-EU1627471582747158single base substitutionGAdownstream_gene_variant
BRCA-EU1627471582747158single base substitutionGAintron_variant
BRCA-EU1627474632747463single base substitutionAGdownstream_gene_variant
BRCA-EU1627474632747463single base substitutionAGintron_variant
BRCA-EU1627479552747955single base substitutionTGdownstream_gene_variant
BRCA-EU1627479552747955single base substitutionTGexon_variant
BRCA-EU1627479552747955single base substitutionTGintron_variant
BRCA-EU1627479552747955single base substitutionTGmissense_variantL137R410T>G
BRCA-EU1627482102748210single base substitutionGAdownstream_gene_variant
BRCA-EU1627482102748210single base substitutionGAintron_variant
BRCA-EU1627485812748581single base substitutionGAdownstream_gene_variant
BRCA-EU1627485812748581single base substitutionGAintron_variant
BRCA-EU1627499882749988single base substitutionCGdownstream_gene_variant
BRCA-EU1627499882749988single base substitutionCGintron_variant
BRCA-EU1627499882749988single base substitutionCTdownstream_gene_variant
BRCA-EU1627499882749988single base substitutionCTintron_variant
BRCA-EU1627501312750131single base substitutionCTdownstream_gene_variant
BRCA-EU1627501312750131single base substitutionCTintron_variant
BRCA-EU1627504072750407single base substitutionGTdownstream_gene_variant
BRCA-EU1627504072750407single base substitutionGTintron_variant
BRCA-EU1627504882750488single base substitutionAGdownstream_gene_variant
BRCA-EU1627504882750488single base substitutionAGintron_variant
BRCA-EU1627507172750717single base substitutionAGdownstream_gene_variant
BRCA-EU1627507172750717single base substitutionAGintron_variant
BRCA-EU1627511342751134single base substitutionGAdownstream_gene_variant
BRCA-EU1627511342751134single base substitutionGAintron_variant
BRCA-EU1627511352751135single base substitutionGTdownstream_gene_variant
BRCA-EU1627511352751135single base substitutionGTintron_variant
BRCA-EU1627519142751914single base substitutionGAdownstream_gene_variant
BRCA-EU1627519142751914single base substitutionGAintron_variant
BRCA-EU1627525782752578single base substitutionCTdownstream_gene_variant
BRCA-EU1627525782752578single base substitutionCTintron_variant
BRCA-EU1627526282752628single base substitutionGCdownstream_gene_variant
BRCA-EU1627526282752628single base substitutionGCintron_variant
BRCA-EU1627530942753094single base substitutionGAdownstream_gene_variant
BRCA-EU1627530942753094single base substitutionGAintron_variant
BRCA-EU1627531162753116single base substitutionTAdownstream_gene_variant
BRCA-EU1627531162753116single base substitutionTAintron_variant
BRCA-EU1627531172753117single base substitutionGTdownstream_gene_variant
BRCA-EU1627531172753117single base substitutionGTintron_variant
BRCA-EU1627540582754058single base substitutionGCdownstream_gene_variant
BRCA-EU1627540582754058single base substitutionGCintron_variant
BRCA-EU1627540592754059single base substitutionATdownstream_gene_variant
BRCA-EU1627540592754059single base substitutionATintron_variant
BRCA-EU1627544872754487single base substitutionCAintron_variant
BRCA-EU1627547032754703single base substitutionAGintron_variant
BRCA-EU1627567312756731single base substitutionGAintron_variant
BRCA-EU1627575042757504single base substitutionCT3_prime_UTR_variant
BRCA-EU1627575042757504single base substitutionCTdownstream_gene_variant
BRCA-EU1627599342759934single base substitutionCGdownstream_gene_variant
BRCA-EU1627616502761650single base substitutionCTdownstream_gene_variant
BRCA-EU1627622132762213single base substitutionGAdownstream_gene_variant
BRCA-FR1627284602728460single base substitutionCTupstream_gene_variant
BRCA-FR1627336322733632single base substitutionGTintron_variant
BRCA-FR1627336322733632single base substitutionGTupstream_gene_variant
BRCA-FR1627340262734026single base substitutionCGintron_variant
BRCA-FR1627340262734026single base substitutionCGupstream_gene_variant
BRCA-FR1627485812748581single base substitutionGAdownstream_gene_variant
BRCA-FR1627485812748581single base substitutionGAintron_variant
BRCA-FR1627499882749988single base substitutionCGdownstream_gene_variant
BRCA-FR1627499882749988single base substitutionCGintron_variant
BRCA-FR1627504882750488single base substitutionAGdownstream_gene_variant
BRCA-FR1627504882750488single base substitutionAGintron_variant
BRCA-FR1627531162753116single base substitutionTAdownstream_gene_variant
BRCA-FR1627531162753116single base substitutionTAintron_variant
BRCA-FR1627531172753117single base substitutionGTdownstream_gene_variant
BRCA-FR1627531172753117single base substitutionGTintron_variant
BRCA-FR1627544872754487single base substitutionCAintron_variant
BRCA-FR1627616502761650single base substitutionCTdownstream_gene_variant
BRCA-FR1627628432762843single base substitutionAGdownstream_gene_variant
BRCA-KR1627626112762611single base substitutionCAdownstream_gene_variant
BRCA-UK1627298722729872single base substitutionGAupstream_gene_variant
BRCA-UK1627539352753935single base substitutionCTdownstream_gene_variant
BRCA-UK1627539352753935single base substitutionCTintron_variant
BRCA-UK1627567242756724single base substitutionGTintron_variant
BRCA-US1627459592745959single base substitutionCTexon_variant
BRCA-US1627459592745959single base substitutionCTsynonymous_variantI92I276C>T
BRCA-US1627626222762622single base substitutionCTdownstream_gene_variant
BRCA-US1627627262762726single base substitutionCGdownstream_gene_variant
BRCA-US1627636232763623single base substitutionGAdownstream_gene_variant
BTCA-JP1627627602762760single base substitutionCAdownstream_gene_variant
BTCA-JP1627628262762826single base substitutionCTdownstream_gene_variant
CLLE-ES1627405872740587single base substitutionGAintron_variant
CLLE-ES1627524092752409single base substitutionTCdownstream_gene_variant
CLLE-ES1627524092752409single base substitutionTCmissense_variantL202P605T>C
CLLE-ES1627524092752409single base substitutionTCsynonymous_variantP171P513T>C
COAD-US1627499012749901single base substitutionGAdownstream_gene_variant
COAD-US1627499012749901single base substitutionGAmissense_variantG178D533G>A
COAD-US1627499012749901single base substitutionGAsynonymous_variantR147R441G>A
COCA-CN1627479462747946single base substitutionTGdownstream_gene_variant
COCA-CN1627479462747946single base substitutionTGexon_variant
COCA-CN1627479462747946single base substitutionTGintron_variant
COCA-CN1627479462747946single base substitutionTGstop_gainedL134*401T>G
COCA-CN1627491512749151single base substitutionCTdownstream_gene_variant
COCA-CN1627491512749151single base substitutionCTintron_variant
COCA-CN1627636492763649single base substitutionCTdownstream_gene_variant
EOPC-DE1627434282743428single base substitutionACintron_variant
ESAD-UK1627313192731319single base substitutionCTupstream_gene_variant
ESAD-UK1627347742734774single base substitutionATintron_variant
ESAD-UK1627347742734774single base substitutionATupstream_gene_variant
ESAD-UK1627375082737508single base substitutionCTintron_variant
ESAD-UK1627376632737663single base substitutionGAintron_variant
ESAD-UK1627379482737948deletion of <=200bpT-intron_variant
ESAD-UK1627382322738232insertion of <=200bp-AAintron_variant
ESAD-UK1627382982738298single base substitutionCGintron_variant
ESAD-UK1627401712740171single base substitutionCTintron_variant
ESAD-UK1627408202740820single base substitutionGAintron_variant
ESAD-UK1627419722741972single base substitutionGAintron_variant
ESAD-UK1627481672748167single base substitutionCTdownstream_gene_variant
ESAD-UK1627481672748167single base substitutionCTintron_variant
ESAD-UK1627511112751111single base substitutionCTdownstream_gene_variant
ESAD-UK1627511112751111single base substitutionCTintron_variant
ESAD-UK1627523282752328single base substitutionGAdownstream_gene_variant
ESAD-UK1627523282752328single base substitutionGAintron_variant
ESAD-UK1627557562755756single base substitutionAGintron_variant
ESAD-UK1627574612757461deletion of <=200bpT-3_prime_UTR_variant
ESAD-UK1627582312758231single base substitutionCT3_prime_UTR_variant
ESAD-UK1627582312758231single base substitutionCTdownstream_gene_variant
ESAD-UK1627584772758477single base substitutionCA3_prime_UTR_variant
ESAD-UK1627584772758477single base substitutionCAdownstream_gene_variant
ESAD-UK1627593192759319single base substitutionGAdownstream_gene_variant
ESAD-UK1627615542761554single base substitutionCTdownstream_gene_variant
ESAD-UK1627628842762884single base substitutionGTdownstream_gene_variant
ESCA-CN1627327472732747single base substitutionGCexon_variant
ESCA-CN1627327472732747single base substitutionGCsynonymous_variantP66P198G>C
ESCA-CN1627327472732747single base substitutionGCupstream_gene_variant
KIRP-US1627627572762757single base substitutionACdownstream_gene_variant
LAML-KR1627304912730491single base substitutionCGupstream_gene_variant
LAML-KR1627524962752496single base substitutionCAdownstream_gene_variant
LAML-KR1627524962752496single base substitutionCAintron_variant
LGG-US1627627572762757single base substitutionACdownstream_gene_variant
LIHC-US1627327262732726single base substitutionGAexon_variant
LIHC-US1627327262732726single base substitutionGAsynonymous_variantR59R177G>A
LIHC-US1627327262732726single base substitutionGAupstream_gene_variant
LINC-JP1627608002760800single base substitutionAGdownstream_gene_variant
LIRI-JP1627281992728199insertion of <=200bp-AGGAGAGTGGCTCTCTCAGupstream_gene_variant
LIRI-JP1627296262729626single base substitutionGCupstream_gene_variant
LIRI-JP1627296922729692single base substitutionGAupstream_gene_variant
LIRI-JP1627300602730061deletion of <=200bpAC-upstream_gene_variant
LIRI-JP1627305462730546single base substitutionATupstream_gene_variant
LIRI-JP1627429092742909single base substitutionGAintron_variant
LIRI-JP1627473392747339single base substitutionGAdownstream_gene_variant
LIRI-JP1627473392747339single base substitutionGAintron_variant
LIRI-JP1627478382747838single base substitutionTGdownstream_gene_variant
LIRI-JP1627478382747838single base substitutionTGintron_variant
LIRI-JP1627491352749135single base substitutionCAdownstream_gene_variant
LIRI-JP1627491352749135single base substitutionCAintron_variant
LIRI-JP1627560872756087single base substitutionGTintron_variant
LIRI-JP1627562952756296deletion of <=200bpCT-intron_variant
LIRI-JP1627591472759147single base substitutionAGdownstream_gene_variant
LIRI-JP1627625172762517insertion of <=200bp-Gdownstream_gene_variant
LUSC-KR1627280132728013single base substitutionCAupstream_gene_variant
LUSC-KR1627280282728028single base substitutionGAupstream_gene_variant
LUSC-KR1627285582728558single base substitutionGCupstream_gene_variant
LUSC-KR1627309462730946single base substitutionTAupstream_gene_variant
LUSC-KR1627327292732729single base substitutionGTexon_variant
LUSC-KR1627327292732729single base substitutionGTmissense_variantQ60H180G>T
LUSC-KR1627327292732729single base substitutionGTupstream_gene_variant
LUSC-KR1627396262739626single base substitutionGTintron_variant
LUSC-KR1627433332743333single base substitutionCGintron_variant
LUSC-KR1627435492743549single base substitutionGTintron_variant
LUSC-KR1627534082753408single base substitutionCAdownstream_gene_variant
LUSC-KR1627534082753408single base substitutionCAintron_variant
LUSC-US1627498422749842single base substitutionCTdownstream_gene_variant
LUSC-US1627498422749842single base substitutionCTmissense_variantP128S382C>T
LUSC-US1627498422749842single base substitutionCTsynonymous_variantY158Y474C>T
MALY-DE1627369642736964single base substitutionCTintron_variant
MALY-DE1627509382750938single base substitutionGAdownstream_gene_variant
MALY-DE1627509382750938single base substitutionGAintron_variant
MALY-DE1627513642751364single base substitutionCTdownstream_gene_variant
MALY-DE1627513642751364single base substitutionCTintron_variant
MALY-DE1627520542752054single base substitutionGAdownstream_gene_variant
MALY-DE1627520542752054single base substitutionGAintron_variant
MALY-DE1627520752752075single base substitutionCGdownstream_gene_variant
MALY-DE1627520752752075single base substitutionCGintron_variant
MALY-DE1627582342758234single base substitutionGA3_prime_UTR_variant
MALY-DE1627582342758234single base substitutionGAdownstream_gene_variant
MELA-AU1627275392727539single base substitutionAGupstream_gene_variant
MELA-AU1627277072727707single base substitutionGAupstream_gene_variant
MELA-AU1627278842727884single base substitutionGAupstream_gene_variant
MELA-AU1627282232728223single base substitutionGAupstream_gene_variant
MELA-AU1627301252730125single base substitutionCTupstream_gene_variant
MELA-AU1627302942730294single base substitutionGAupstream_gene_variant
MELA-AU1627310682731068single base substitutionGAupstream_gene_variant
MELA-AU1627313882731388single base substitutionAGupstream_gene_variant
MELA-AU1627324202732420single base substitutionCTupstream_gene_variant
MELA-AU1627324212732421single base substitutionCTupstream_gene_variant
MELA-AU1627325612732561single base substitutionTAexon_variant
MELA-AU1627325612732561single base substitutionTAmissense_variantN4K12T>A
MELA-AU1627325612732561single base substitutionTAupstream_gene_variant
MELA-AU1627343942734394single base substitutionCTintron_variant
MELA-AU1627343942734394single base substitutionCTupstream_gene_variant
MELA-AU1627350392735039single base substitutionCTintron_variant
MELA-AU1627350392735039single base substitutionCTupstream_gene_variant
MELA-AU1627369202736920single base substitutionGAintron_variant
MELA-AU1627370702737070single base substitutionCTintron_variant
MELA-AU1627372052737205single base substitutionCTintron_variant
MELA-AU1627372062737206single base substitutionCTintron_variant
MELA-AU1627380012738001single base substitutionCTintron_variant
MELA-AU1627382042738204single base substitutionTCintron_variant
MELA-AU1627382702738270single base substitutionGCintron_variant
MELA-AU1627399772739977single base substitutionCTintron_variant
MELA-AU1627402932740293single base substitutionCTintron_variant
MELA-AU1627408942740894single base substitutionCTintron_variant
MELA-AU1627409572740957single base substitutionCAintron_variant
MELA-AU1627419542741954single base substitutionCTintron_variant
MELA-AU1627424432742443single base substitutionCTintron_variant
MELA-AU1627433652743365single base substitutionGAintron_variant
MELA-AU1627434642743464single base substitutionCTintron_variant
MELA-AU1627475032747503single base substitutionCTdownstream_gene_variant
MELA-AU1627475032747503single base substitutionCTintron_variant
MELA-AU1627475362747536single base substitutionGTdownstream_gene_variant
MELA-AU1627475362747536single base substitutionGTintron_variant
MELA-AU1627475542747554single base substitutionCTdownstream_gene_variant
MELA-AU1627475542747554single base substitutionCTintron_variant
MELA-AU1627480542748054single base substitutionCTdownstream_gene_variant
MELA-AU1627480542748054single base substitutionCTintron_variant
MELA-AU1627481842748184single base substitutionCTdownstream_gene_variant
MELA-AU1627481842748184single base substitutionCTintron_variant
MELA-AU1627484192748419single base substitutionGAdownstream_gene_variant
MELA-AU1627484192748419single base substitutionGAintron_variant
MELA-AU1627485792748579single base substitutionCTdownstream_gene_variant
MELA-AU1627485792748579single base substitutionCTintron_variant
MELA-AU1627487852748785single base substitutionCTdownstream_gene_variant
MELA-AU1627487852748785single base substitutionCTintron_variant
MELA-AU1627491502749150single base substitutionCTdownstream_gene_variant
MELA-AU1627491502749150single base substitutionCTintron_variant
MELA-AU1627492322749232single base substitutionCTdownstream_gene_variant
MELA-AU1627492322749232single base substitutionCTexon_variant
MELA-AU1627492322749232single base substitutionCTintron_variant
MELA-AU1627497382749739multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1627497382749739multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1627498142749815multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1627498142749815multiple base substitution (>=2bp and <=200bp)CCTTsplice_region_variant
MELA-AU1627506242750624single base substitutionCAdownstream_gene_variant
MELA-AU1627506242750624single base substitutionCAintron_variant
MELA-AU1627506322750632single base substitutionCTdownstream_gene_variant
MELA-AU1627506322750632single base substitutionCTintron_variant
MELA-AU1627507342750734single base substitutionCTdownstream_gene_variant
MELA-AU1627507342750734single base substitutionCTintron_variant
MELA-AU1627508772750877single base substitutionCTdownstream_gene_variant
MELA-AU1627508772750877single base substitutionCTintron_variant
MELA-AU1627509532750953single base substitutionCTdownstream_gene_variant
MELA-AU1627509532750953single base substitutionCTintron_variant
MELA-AU1627514632751463single base substitutionCTdownstream_gene_variant
MELA-AU1627514632751463single base substitutionCTintron_variant
MELA-AU1627520752752075single base substitutionCTdownstream_gene_variant
MELA-AU1627520752752075single base substitutionCTintron_variant
MELA-AU1627522282752228single base substitutionCTdownstream_gene_variant
MELA-AU1627522282752228single base substitutionCTintron_variant
MELA-AU1627531462753146single base substitutionGTdownstream_gene_variant
MELA-AU1627531462753146single base substitutionGTintron_variant
MELA-AU1627531932753193single base substitutionCTdownstream_gene_variant
MELA-AU1627531932753193single base substitutionCTintron_variant
MELA-AU1627535932753594multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1627535932753594multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1627535942753594single base substitutionCTdownstream_gene_variant
MELA-AU1627535942753594single base substitutionCTintron_variant
MELA-AU1627539462753946single base substitutionCTdownstream_gene_variant
MELA-AU1627539462753946single base substitutionCTintron_variant
MELA-AU1627540342754034single base substitutionCTdownstream_gene_variant
MELA-AU1627540342754034single base substitutionCTintron_variant
MELA-AU1627541022754102single base substitutionCTdownstream_gene_variant
MELA-AU1627541022754102single base substitutionCTintron_variant
MELA-AU1627544992754499single base substitutionCTintron_variant
MELA-AU1627546952754695single base substitutionCTintron_variant
MELA-AU1627547652754765single base substitutionCTintron_variant
MELA-AU1627548032754803single base substitutionGAintron_variant
MELA-AU1627550192755019single base substitutionCTintron_variant
MELA-AU1627550662755066single base substitutionCTintron_variant
MELA-AU1627551912755191single base substitutionCTintron_variant
MELA-AU1627552492755249single base substitutionCTintron_variant
MELA-AU1627560992756099single base substitutionCTintron_variant
MELA-AU1627561002756100single base substitutionCTintron_variant
MELA-AU1627563532756353single base substitutionGAintron_variant
MELA-AU1627566912756691single base substitutionCTintron_variant
MELA-AU1627570082757008single base substitutionCTintron_variant
MELA-AU1627571342757134single base substitutionCTintron_variant
MELA-AU1627573182757318single base substitutionCTmissense_variantS232L695C>T
MELA-AU1627573182757318single base substitutionCTsynonymous_variantL201L603C>T
MELA-AU1627579162757916single base substitutionCT3_prime_UTR_variant
MELA-AU1627579162757916single base substitutionCTdownstream_gene_variant
MELA-AU1627584832758483single base substitutionCT3_prime_UTR_variant
MELA-AU1627584832758483single base substitutionCTdownstream_gene_variant
MELA-AU1627589592758959single base substitutionCT3_prime_UTR_variant
MELA-AU1627589592758959single base substitutionCTdownstream_gene_variant
MELA-AU1627592312759231single base substitutionCTdownstream_gene_variant
MELA-AU1627592632759263single base substitutionCTdownstream_gene_variant
MELA-AU1627593132759313single base substitutionGAdownstream_gene_variant
MELA-AU1627593242759324single base substitutionCTdownstream_gene_variant
MELA-AU1627593482759348single base substitutionCTdownstream_gene_variant
MELA-AU1627595692759570multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU1627596582759658single base substitutionCTdownstream_gene_variant
MELA-AU1627604812760481single base substitutionCAdownstream_gene_variant
MELA-AU1627614982761498single base substitutionGAdownstream_gene_variant
MELA-AU1627615392761539single base substitutionCTdownstream_gene_variant
MELA-AU1627616832761683single base substitutionCTdownstream_gene_variant
MELA-AU1627628452762845single base substitutionCAdownstream_gene_variant
MELA-AU1627632922763292single base substitutionGAdownstream_gene_variant
MELA-AU1627639782763978single base substitutionGAdownstream_gene_variant
ORCA-IN1627469532746953single base substitutionCTdownstream_gene_variant
ORCA-IN1627469532746953single base substitutionCTintron_variant
ORCA-IN1627606802760680single base substitutionGCdownstream_gene_variant
OV-AU1627281712728171single base substitutionATupstream_gene_variant
OV-AU1627287002728700single base substitutionGAupstream_gene_variant
OV-AU1627314562731456single base substitutionCTupstream_gene_variant
OV-AU1627402432740243single base substitutionGAintron_variant
OV-AU1627461852746185single base substitutionGCdownstream_gene_variant
OV-AU1627461852746185single base substitutionGCintron_variant
OV-AU1627475872747587single base substitutionGAdownstream_gene_variant
OV-AU1627475872747587single base substitutionGAintron_variant
OV-AU1627572402757240single base substitutionCTintron_variant
OV-AU1627585882758588single base substitutionAG3_prime_UTR_variant
OV-AU1627585882758588single base substitutionAGdownstream_gene_variant
OV-AU1627630892763089single base substitutionGTdownstream_gene_variant
OV-AU1627640302764030single base substitutionCTdownstream_gene_variant
PACA-AU1627326542732654single base substitutionGAexon_variant
PACA-AU1627326542732654single base substitutionGAsynonymous_variantL35L105G>A
PACA-AU1627326542732654single base substitutionGAupstream_gene_variant
PACA-AU1627409832740983single base substitutionGAintron_variant
PACA-AU1627517242751724single base substitutionGAdownstream_gene_variant
PACA-AU1627517242751724single base substitutionGAintron_variant
PACA-AU1627524462752446single base substitutionCTdownstream_gene_variant
PACA-AU1627524462752446single base substitutionCTmissense_variantR184W550C>T
PACA-AU1627524462752446single base substitutionCTsynonymous_variantY214Y642C>T
PACA-AU1627539472753947single base substitutionGAdownstream_gene_variant
PACA-AU1627539472753947single base substitutionGAintron_variant
PACA-AU1627554642755464single base substitutionGTintron_variant
PACA-AU1627592982759298single base substitutionAGdownstream_gene_variant
PACA-AU1627626332762633single base substitutionGAdownstream_gene_variant
PACA-AU1627628262762826single base substitutionCTdownstream_gene_variant
PACA-AU1627633072763307single base substitutionGAdownstream_gene_variant
PACA-CA1627325742732574single base substitutionCAexon_variant
PACA-CA1627325742732574single base substitutionCAmissense_variantL9M25C>A
PACA-CA1627325742732574single base substitutionCAupstream_gene_variant
PACA-CA1627334482733448single base substitutionTAintron_variant
PACA-CA1627334482733448single base substitutionTAupstream_gene_variant
PACA-CA1627348102734810single base substitutionGAintron_variant
PACA-CA1627348102734810single base substitutionGAupstream_gene_variant
PACA-CA1627352772735277single base substitutionACintron_variant
PACA-CA1627352772735277single base substitutionACupstream_gene_variant
PACA-CA1627428052742805single base substitutionCTintron_variant
PACA-CA1627470992747099single base substitutionCGdownstream_gene_variant
PACA-CA1627470992747099single base substitutionCGintron_variant
PACA-CA1627486632748663single base substitutionCTdownstream_gene_variant
PACA-CA1627486632748663single base substitutionCTintron_variant
PACA-CA1627492402749240single base substitutionCTdownstream_gene_variant
PACA-CA1627492402749240single base substitutionCTexon_variant
PACA-CA1627492402749240single base substitutionCTintron_variant
PACA-CA1627496582749658single base substitutionGAdownstream_gene_variant
PACA-CA1627496582749658single base substitutionGAintron_variant
PACA-CA1627502232750223single base substitutionCTdownstream_gene_variant
PACA-CA1627502232750223single base substitutionCTintron_variant
PACA-CA1627524022752402single base substitutionGAdownstream_gene_variant
PACA-CA1627524022752402single base substitutionGAmissense_variantE200K598G>A
PACA-CA1627524022752402single base substitutionGAmissense_variantR169Q506G>A
PACA-CA1627532922753292single base substitutionTAdownstream_gene_variant
PACA-CA1627532922753292single base substitutionTAintron_variant
PACA-CA1627577142757714single base substitutionGA3_prime_UTR_variant
PACA-CA1627577142757714single base substitutionGAdownstream_gene_variant
PACA-CA1627579892757989single base substitutionCT3_prime_UTR_variant
PACA-CA1627579892757989single base substitutionCTdownstream_gene_variant
PACA-CA1627590642759064single base substitutionCTdownstream_gene_variant
PACA-CA1627617432761744deletion of <=200bpCT-downstream_gene_variant
PAEN-AU1627348692734869single base substitutionGCintron_variant
PAEN-AU1627348692734869single base substitutionGCupstream_gene_variant
PAEN-IT1627317292731729single base substitutionCAupstream_gene_variant
PAEN-IT1627513732751373single base substitutionGAdownstream_gene_variant
PAEN-IT1627513732751373single base substitutionGAintron_variant
PBCA-DE1627548562754856single base substitutionGAintron_variant
PBCA-DE1627560812756081single base substitutionCTintron_variant
PBCA-DE1627576942757694single base substitutionGT3_prime_UTR_variant
PBCA-DE1627576942757694single base substitutionGTdownstream_gene_variant
PRAD-CA1627382252738225single base substitutionATintron_variant
PRAD-CA1627382292738229single base substitutionATintron_variant
PRAD-CA1627600262760026single base substitutionCAdownstream_gene_variant
PRAD-UK1627354062735406single base substitutionCTintron_variant
PRAD-UK1627354062735406single base substitutionCTupstream_gene_variant
PRAD-UK1627402742740274single base substitutionCTintron_variant
PRAD-UK1627407962740796single base substitutionCTintron_variant
PRAD-UK1627436752743683deletion of <=200bpCGCCCAGCA-intron_variant
RECA-EU1627285562728556single base substitutionTCupstream_gene_variant
RECA-EU1627324202732420single base substitutionCTupstream_gene_variant
RECA-EU1627370942737094single base substitutionCTintron_variant
RECA-EU1627559512755951single base substitutionGAintron_variant
SKCA-BR1627275222727522single base substitutionGAupstream_gene_variant
SKCA-BR1627284062728406single base substitutionCTupstream_gene_variant
SKCA-BR1627285582728558single base substitutionGCupstream_gene_variant
SKCA-BR1627288452728845single base substitutionTGupstream_gene_variant
SKCA-BR1627312952731295single base substitutionCTupstream_gene_variant
SKCA-BR1627353112735311single base substitutionCTintron_variant
SKCA-BR1627353112735311single base substitutionCTupstream_gene_variant
SKCA-BR1627385132738513single base substitutionACintron_variant
SKCA-BR1627395372739537single base substitutionGTintron_variant
SKCA-BR1627414152741415single base substitutionTCintron_variant
SKCA-BR1627416632741663single base substitutionCTintron_variant
SKCA-BR1627486072748607single base substitutionACdownstream_gene_variant
SKCA-BR1627486072748607single base substitutionACintron_variant
SKCA-BR1627486962748696single base substitutionCTdownstream_gene_variant
SKCA-BR1627486962748696single base substitutionCTintron_variant
SKCA-BR1627492712749271single base substitutionACdownstream_gene_variant
SKCA-BR1627492712749271single base substitutionACexon_variant
SKCA-BR1627492712749271single base substitutionACintron_variant
SKCA-BR1627507532750753single base substitutionCTdownstream_gene_variant
SKCA-BR1627507532750753single base substitutionCTintron_variant
SKCA-BR1627508042750805deletion of <=200bpGC-downstream_gene_variant
SKCA-BR1627508042750805deletion of <=200bpGC-intron_variant
SKCA-BR1627627572762757single base substitutionACdownstream_gene_variant
SKCA-BR1627627662762766single base substitutionTCdownstream_gene_variant
SKCM-US1627326872732687single base substitutionCTexon_variant
SKCM-US1627326872732687single base substitutionCTsynonymous_variantV46V138C>T
SKCM-US1627326872732687single base substitutionCTupstream_gene_variant
SKCM-US1627327532732753single base substitutionCTexon_variant
SKCM-US1627327532732753single base substitutionCTsynonymous_variantS68S204C>T
SKCM-US1627327532732753single base substitutionCTupstream_gene_variant
SKCM-US1627479942747994single base substitutionCTdownstream_gene_variant
SKCM-US1627479942747994single base substitutionCTexon_variant
SKCM-US1627479942747994single base substitutionCTintron_variant
SKCM-US1627479942747994single base substitutionCTmissense_variantS150L449C>T
SKCM-US1627498292749829single base substitutionTGdownstream_gene_variant
SKCM-US1627498292749829single base substitutionTGmissense_variantC123W369T>G
SKCM-US1627498292749829single base substitutionTGmissense_variantV154G461T>G
SKCM-US1627573142757314single base substitutionGAmissense_variantG231S691G>A
SKCM-US1627573142757314single base substitutionGAmissense_variantR200K599G>A
SKCM-US1627573182757318single base substitutionCTmissense_variantS232L695C>T
SKCM-US1627573182757318single base substitutionCTsynonymous_variantL201L603C>T
SKCM-US1627627322762732single base substitutionGAdownstream_gene_variant
SKCM-US1627635672763567single base substitutionCTdownstream_gene_variant
STAD-US1627523892752389single base substitutionCTdownstream_gene_variant
STAD-US1627523892752389single base substitutionCTstop_gainedR165*493C>T
STAD-US1627523892752389single base substitutionCTsynonymous_variantN195N585C>T
STAD-US1627636832763683single base substitutionCTdownstream_gene_variant
UCEC-US1627460342746034single base substitutionCTdownstream_gene_variant
UCEC-US1627460342746034single base substitutionCTexon_variant
UCEC-US1627460342746034single base substitutionCTsynonymous_variantL117L351C>T
UCEC-US1627479782747978single base substitutionCTdownstream_gene_variant
UCEC-US1627479782747978single base substitutionCTexon_variant
UCEC-US1627479782747978single base substitutionCTintron_variant
UCEC-US1627479782747978single base substitutionCTstop_gainedR145*433C>T
UCEC-US1627523762752376single base substitutionAGdownstream_gene_variant
UCEC-US1627523762752376single base substitutionAGmissense_variantY191C572A>G
UCEC-US1627523762752376single base substitutionAGsynonymous_variantL160L480A>G
UCEC-US1627524152752415single base substitutionTGdownstream_gene_variant
UCEC-US1627524152752415single base substitutionTGmissense_variantC173W519T>G
UCEC-US1627524152752415single base substitutionTGmissense_variantV204G611T>G
UCEC-US1627636732763673single base substitutionGAdownstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
SJHYPO016COSM4775503c.551_554delTGGTp.L184fs*>50Deletion - Frameshift16:2702354-2702357+
PCSI_0297_Pa_P_526COSM4962506c.25C>Ap.L9MSubstitution - Missense16:2682573-2682573+
TCGA-EP-A26S-01COSM4913578c.177G>Ap.R59RSubstitution - coding silent16:2682725-2682725+
184COSM145538c.605T>Cp.L202PSubstitution - Missense16:2702408-2702408+
ESCC_BICR_012TCOSM5433066c.198G>Cp.P66PSubstitution - coding silent16:2682746-2682746+
PT49COSM5936216c.637C>Tp.P213SSubstitution - Missense16:2702440-2702440+
TCGA-GN-A265-06COSM3508172c.204C>Tp.S68SSubstitution - coding silent16:2682752-2682752+
C008COSM5522953c.108C>Tp.A36ASubstitution - coding silent16:2682656-2682656+
T3021COSM4694825c.472T>Cp.Y158HSubstitution - Missense16:2699839-2699839+
TCGA-B5-A11E-01COSM969247c.433C>Tp.R145*Substitution - Nonsense16:2697977-2697977+
TCGA-AA-3492-01COSM1376992c.533G>Ap.G178DSubstitution - Missense16:2699900-2699900+
TCGA-D1-A15X-01COSM969269c.572A>Gp.Y191CSubstitution - Missense16:2702375-2702375+
TCGA-FS-A1ZK-06COSM3508221c.461T>Gp.V154GSubstitution - Missense16:2699828-2699828+
Au5COSM702820c.474C>Tp.Y158YSubstitution - coding silent16:2699841-2699841+
184-01-4TDCOSM145538c.605T>Cp.L202PSubstitution - Missense16:2702408-2702408+
SNUH_G45_S1COSM3999814c.325G>Ap.G109SSubstitution - Missense16:2696007-2696007+
TCGA-D3-A2JP-06COSM3508208c.449C>Tp.S150LSubstitution - Missense16:2697993-2697993+
YUKATCOSM5384611c.514G>Ap.V172MSubstitution - Missense16:2699881-2699881+
61COSM5740528c.119G>Ap.G40DSubstitution - Missense16:2682667-2682667+
CCK81COSM3108949c.650C>Tp.A217VSubstitution - Missense16:2702453-2702453+
TCGA-FS-A1ZZ-06COSM3508171c.138C>Tp.V46VSubstitution - coding silent16:2682686-2682686+
PCSI_0024_Pa_XCOSM1158486c.598G>Ap.E200KSubstitution - Missense16:2702401-2702401+
PCSI_0024_Pa_CCOSM1158486c.598G>Ap.E200KSubstitution - Missense16:2702401-2702401+
CSCC-11-TCOSM4545246c.373G>Ap.E125KSubstitution - Missense16:2697917-2697917+
PD4874aCOSM5800888c.410T>Gp.L137RSubstitution - Missense16:2697954-2697954+
TCGA-BR-6452-01COSM4059661c.585C>Tp.N195NSubstitution - coding silent16:2702388-2702388+
TCGA-OL-A5RX-01COSM3817649c.276C>Tp.I92ISubstitution - coding silent16:2695958-2695958+
EGC8COSM5054794c.528C>Tp.S176SSubstitution - coding silent16:2699895-2699895+
TCGA-B5-A11E-01COSM969270c.611T>Gp.V204GSubstitution - Missense16:2702414-2702414+
TCGA-66-2756-01COSM702820c.474C>Tp.Y158YSubstitution - coding silent16:2699841-2699841+
8044103COSM3387346c.642C>Tp.Y214YSubstitution - coding silent16:2702445-2702445+
PCSI0024COSM1158486c.598G>Ap.E200KSubstitution - Missense16:2702401-2702401+
TCGA-D1-A17Q-01COSM969242c.351C>Tp.L117LSubstitution - coding silent16:2696033-2696033+
CSCC-44-TCOSM4504277c.660C>Tp.P220PSubstitution - coding silent16:2702463-2702463+
C008COSM5522952c.109C>Tp.Q37*Substitution - Nonsense16:2682657-2682657+
8067235COSM3772175c.105G>Ap.L35LSubstitution - coding silent16:2682653-2682653+
184COSM145538c.605T>Cp.L202PSubstitution - Missense16:2702408-2702408+
J30_TCOSM3957388c.180G>Tp.Q60HSubstitution - Missense16:2682728-2682728+
TCGA-EE-A3J5-06COSM3508240c.691G>Ap.G231SSubstitution - Missense16:2707313-2707313+
TCGA-EE-A2MF-06COSM4892671c.695C>Tp.S232LSubstitution - Missense16:2707317-2707317+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.6196016p13.36112852428953|CGAP|BC007314|C/T|non-coding||2124|Candidate
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
CAMissensep.S221Rc.663C>A162752467STAD
CC-Frameshiftp.V204Gfs*74c.603_604delCC162752407LUAD
CTMissensep.S150Lc.449C>T162747994CM
CTMissensep.S232Lc.695C>T162757318CM
CTSynonymousp.S68Sc.204C>T162732753CM
CTSynonymousp.V46Vc.138C>T162732687CM
CTSynonymousp.Y158Yc.474C>T162749842LUSC
GA3-UTRSNV.c.702+909G>A162758234DLBCL
GAMissensep.G231Sc.691G>A162757314CM
GCMissensep.K84Nc.252G>C162732801ALL
GTMissensep.G15Vc.44G>T162732593STAD
TCMissensep.L202Pc.605T>C162752409CLL
TGGT-SpliceAcceptorDeletion.c.551_554delTGGT162752355ALL
TGMissensep.V154Gc.461T>G162749829CM