RP11-574F21.3
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US1160209813160209813single base substitutionCAdownstream_gene_variant
BLCA-US1160209813160209813single base substitutionCAstop_gainedE287*859G>T
BLCA-US1160253381160253381single base substitutionGAintron_variant
BLCA-US1160253381160253381single base substitutionGAupstream_gene_variant
BRCA-EU1160182625160182625single base substitutionAGdownstream_gene_variant
BRCA-EU1160182980160182980single base substitutionCAdownstream_gene_variant
BRCA-EU1160183122160183122single base substitutionGCdownstream_gene_variant
BRCA-EU1160183264160183264single base substitutionGAdownstream_gene_variant
BRCA-EU1160183305160183305single base substitutionGAdownstream_gene_variant
BRCA-EU1160184665160184665single base substitutionCTdownstream_gene_variant
BRCA-EU1160185519160185519single base substitutionGCdownstream_gene_variant
BRCA-EU1160185641160185641insertion of <=200bp-Adownstream_gene_variant
BRCA-EU1160189977160189977single base substitutionCAintron_variant
BRCA-EU1160190265160190265deletion of <=200bpG-intron_variant
BRCA-EU1160191053160191053single base substitutionCGintron_variant
BRCA-EU1160191736160191736single base substitutionAGintron_variant
BRCA-EU1160192001160192001single base substitutionTCintron_variant
BRCA-EU1160192962160192962single base substitutionCTintron_variant
BRCA-EU1160194043160194043single base substitutionGCintron_variant
BRCA-EU1160194440160194440single base substitutionCTintron_variant
BRCA-EU1160194944160194944deletion of <=200bpC-intron_variant
BRCA-EU1160195463160195463single base substitutionGCintron_variant
BRCA-EU1160196060160196060single base substitutionGTintron_variant
BRCA-EU1160196128160196128single base substitutionATintron_variant
BRCA-EU1160196478160196478single base substitutionCAintron_variant
BRCA-EU1160196524160196524single base substitutionCGintron_variant
BRCA-EU1160198574160198574single base substitutionTGintron_variant
BRCA-EU1160199085160199085single base substitutionCGintron_variant
BRCA-EU1160199143160199143single base substitutionTCintron_variant
BRCA-EU1160199695160199695single base substitutionCAintron_variant
BRCA-EU1160200318160200318deletion of <=200bpA-intron_variant
BRCA-EU1160200599160200599single base substitutionTCintron_variant
BRCA-EU1160200791160200791single base substitutionCTintron_variant
BRCA-EU1160201408160201408deletion of <=200bpA-intron_variant
BRCA-EU1160201408160201408insertion of <=200bp-Aintron_variant
BRCA-EU1160202131160202131single base substitutionTCintron_variant
BRCA-EU1160202234160202234single base substitutionCAintron_variant
BRCA-EU1160202631160202631single base substitutionCTintron_variant
BRCA-EU1160203457160203457single base substitutionATintron_variant
BRCA-EU1160205155160205155single base substitutionCGdownstream_gene_variant
BRCA-EU1160205155160205155single base substitutionCGintron_variant
BRCA-EU1160206292160206292deletion of <=200bpA-downstream_gene_variant
BRCA-EU1160206292160206292deletion of <=200bpA-intron_variant
BRCA-EU1160206979160206979single base substitutionGAdownstream_gene_variant
BRCA-EU1160206979160206979single base substitutionGAmissense_variantA456V1367C>T
BRCA-EU1160207674160207674single base substitutionGAdownstream_gene_variant
BRCA-EU1160207674160207674single base substitutionGAintron_variant
BRCA-EU1160210400160210400single base substitutionCGintron_variant
BRCA-EU1160210942160210942deletion of <=200bpA-intron_variant
BRCA-EU1160211342160211342single base substitutionAGintron_variant
BRCA-EU1160212018160212018single base substitutionGCintron_variant
BRCA-EU1160213278160213278single base substitutionCGintron_variant
BRCA-EU1160213655160213655single base substitutionCGintron_variant
BRCA-EU1160213742160213742single base substitutionCTintron_variant
BRCA-EU1160213742160213742single base substitutionCTsplice_region_variant
BRCA-EU1160214375160214375single base substitutionCGintron_variant
BRCA-EU1160215207160215207single base substitutionCTintron_variant
BRCA-EU1160215929160215929single base substitutionCGintron_variant
BRCA-EU1160216294160216294single base substitutionGAintron_variant
BRCA-EU1160216744160216744single base substitutionGTintron_variant
BRCA-EU1160216785160216785single base substitutionACintron_variant
BRCA-EU1160217953160217953single base substitutionCTintron_variant
BRCA-EU1160218501160218501single base substitutionAGintron_variant
BRCA-EU1160219485160219523deletion of <=200bpTGAATGTTTTAATAGTTTTACTTAAATTCATCAAAAAAC-intron_variant
BRCA-EU1160219622160219622single base substitutionTCintron_variant
BRCA-EU1160220096160220096single base substitutionGCintron_variant
BRCA-EU1160220327160220327single base substitutionAGintron_variant
BRCA-EU1160220373160220373single base substitutionATintron_variant
BRCA-EU1160220620160220620single base substitutionTGintron_variant
BRCA-EU1160222321160222321single base substitutionAGintron_variant
BRCA-EU1160222569160222569single base substitutionCTintron_variant
BRCA-EU1160223388160223388single base substitutionAGintron_variant
BRCA-EU1160223489160223489single base substitutionATintron_variant
BRCA-EU1160224189160224189single base substitutionACintron_variant
BRCA-EU1160224745160224745single base substitutionTCintron_variant
BRCA-EU1160224965160224965single base substitutionGAintron_variant
BRCA-EU1160225107160225107single base substitutionGAintron_variant
BRCA-EU1160225945160225945single base substitutionGCintron_variant
BRCA-EU1160226546160226546single base substitutionTAintron_variant
BRCA-EU1160226693160226693deletion of <=200bpA-intron_variant
BRCA-EU1160227059160227059single base substitutionTAintron_variant
BRCA-EU1160227060160227060single base substitutionATintron_variant
BRCA-EU1160228387160228390deletion of <=200bpTTTA-intron_variant
BRCA-EU1160228394160228394single base substitutionACintron_variant
BRCA-EU1160228733160228733single base substitutionCGintron_variant
BRCA-EU1160229940160229940single base substitutionGCintron_variant
BRCA-EU1160231493160231493single base substitutionGAintron_variant
BRCA-EU1160232330160232330single base substitutionCGintron_variant
BRCA-EU1160233237160233237single base substitutionAGintron_variant
BRCA-EU1160233237160233237single base substitutionAGmissense_variantM168T503T>C
BRCA-EU1160233428160233428deletion of <=200bpA-intron_variant
BRCA-EU1160234030160234030single base substitutionTCintron_variant
BRCA-EU1160235041160235044deletion of <=200bpATTA-intron_variant
BRCA-EU1160235565160235565single base substitutionGAintron_variant
BRCA-EU1160235921160235921single base substitutionGAintron_variant
BRCA-EU1160236538160236538single base substitutionCAintron_variant
BRCA-EU1160239534160239534single base substitutionGAintron_variant
BRCA-EU1160240442160240443deletion of <=200bpTT-intron_variant
BRCA-EU1160241038160241038single base substitutionACintron_variant
BRCA-EU1160241949160241949single base substitutionTGintron_variant
BRCA-EU1160242014160242014single base substitutionCGintron_variant
BRCA-EU1160242918160242918single base substitutionCTintron_variant
BRCA-EU1160243046160243046single base substitutionGAintron_variant
BRCA-EU1160243103160243103single base substitutionCTintron_variant
BRCA-EU1160243661160243661single base substitutionCTintron_variant
BRCA-EU1160243993160243993single base substitutionGTintron_variant
BRCA-EU1160244137160244137single base substitutionAGintron_variant
BRCA-EU1160244277160244277single base substitutionCTintron_variant
BRCA-EU1160244286160244286single base substitutionGTintron_variant
BRCA-EU1160244381160244381single base substitutionGAintron_variant
BRCA-EU1160245236160245236single base substitutionCGintron_variant
BRCA-EU1160245496160245496single base substitutionGCintron_variant
BRCA-EU1160247710160247710single base substitutionACintron_variant
BRCA-EU1160248911160248911single base substitutionCGintron_variant
BRCA-EU1160249235160249235deletion of <=200bpG-intron_variant
BRCA-EU1160252704160252704single base substitutionGAintron_variant
BRCA-EU1160252704160252704single base substitutionGAupstream_gene_variant
BRCA-EU1160252777160252777single base substitutionCT5_prime_UTR_variant
BRCA-EU1160252777160252777single base substitutionCTupstream_gene_variant
BRCA-EU1160252797160252797single base substitutionCT5_prime_UTR_variant
BRCA-EU1160252797160252797single base substitutionCTupstream_gene_variant
BRCA-EU1160254773160254773single base substitutionCGintron_variant
BRCA-EU1160254773160254773single base substitutionCGupstream_gene_variant
BRCA-EU1160254971160254971single base substitutionCAupstream_gene_variant
BRCA-EU1160255142160255142single base substitutionGAupstream_gene_variant
BRCA-EU1160255562160255562single base substitutionCTupstream_gene_variant
BRCA-EU1160255692160255692single base substitutionCGupstream_gene_variant
BRCA-EU1160256709160256709single base substitutionATupstream_gene_variant
BRCA-EU1160256987160256987single base substitutionCTupstream_gene_variant
BRCA-EU1160257315160257315single base substitutionCTupstream_gene_variant
BRCA-EU1160257638160257638single base substitutionGCupstream_gene_variant
BRCA-EU1160257776160257776single base substitutionACupstream_gene_variant
BRCA-EU1160258770160258770deletion of <=200bpT-upstream_gene_variant
BRCA-EU1160259265160259265single base substitutionCAupstream_gene_variant
BRCA-EU1160259614160259614single base substitutionCGupstream_gene_variant
BRCA-FR1160183264160183264single base substitutionGAdownstream_gene_variant
BRCA-FR1160214375160214375single base substitutionCGintron_variant
BRCA-FR1160221788160221788single base substitutionAGintron_variant
BRCA-FR1160235565160235565single base substitutionGAintron_variant
BRCA-FR1160236538160236538single base substitutionCAintron_variant
BRCA-FR1160238063160238063single base substitutionGAintron_variant
BRCA-FR1160240521160240521single base substitutionTGintron_variant
BRCA-FR1160250093160250093single base substitutionTCintron_variant
BRCA-FR1160257638160257638single base substitutionGCupstream_gene_variant
BRCA-UK1160182625160182625single base substitutionAGdownstream_gene_variant
BRCA-UK1160215762160215762single base substitutionCGintron_variant
BRCA-UK1160252704160252704single base substitutionGAintron_variant
BRCA-UK1160252704160252704single base substitutionGAupstream_gene_variant
BRCA-US1160183048160183048single base substitutionGAdownstream_gene_variant
BRCA-US1160195422160195422single base substitutionCGmissense_variantE522Q1564G>C
BRCA-US1160209535160209535single base substitutionCGdownstream_gene_variant
BRCA-US1160209535160209535single base substitutionCGsynonymous_variantR379R1137G>C
BRCA-US1160209851160209851single base substitutionCTdownstream_gene_variant
BRCA-US1160209851160209851single base substitutionCTmissense_variantR274H821G>A
BRCA-US1160210108160210108single base substitutionCTsynonymous_variantE188E564G>A
BRCA-US1160210108160210108single base substitutionCTsynonymous_variantE246E738G>A
BRCA-US1160213762160213762single base substitutionCGintron_variant
BRCA-US1160213762160213762single base substitutionCGmissense_variantD167H499G>C
BRCA-US1160251960160251960single base substitutionTCmissense_variantK25E73A>G
BRCA-US1160251960160251960single base substitutionTCmissense_variantK8E22A>G
BRCA-US1160252800160252800single base substitutionAC5_prime_UTR_variant
BRCA-US1160252800160252800single base substitutionACupstream_gene_variant
BTCA-JP1160188012160188012single base substitutionGAintron_variant
BTCA-JP1160192539160192539single base substitutionCTmissense_variantE602K1804G>A
BTCA-JP1160194944160194944deletion of <=200bpC-intron_variant
BTCA-JP1160194944160194944insertion of <=200bp-Cintron_variant
BTCA-JP1160208624160208624single base substitutionTGdownstream_gene_variant
BTCA-JP1160208624160208624single base substitutionTGintron_variant
BTCA-JP1160208661160208661single base substitutionTAdownstream_gene_variant
BTCA-JP1160208661160208661single base substitutionTAintron_variant
CESC-US1160187440160187440single base substitutionGAmissense_variantS733F2198C>T
CESC-US1160188831160188831single base substitutionGAintron_variant
CESC-US1160208574160208574single base substitutionGCdownstream_gene_variant
CESC-US1160208574160208574single base substitutionGCintron_variant
CESC-US1160249105160249105single base substitutionGCintron_variant
CESC-US1160249182160249182deletion of <=200bpG-intron_variant
CLLE-ES1160210197160210197single base substitutionACintron_variant
CLLE-ES1160219456160219456single base substitutionTCintron_variant
COAD-US1160187476160187476single base substitutionCAmissense_variantG721V2162G>T
COAD-US1160201110160201110single base substitutionCTsynonymous_variantV503V1509G>A
COAD-US1160251976160251976single base substitutionCTsynonymous_variantS19S57G>A
COAD-US1160251976160251976single base substitutionCTsynonymous_variantS2S6G>A
COAD-US1160253413160253413single base substitutionGAintron_variant
COAD-US1160253413160253413single base substitutionGAupstream_gene_variant
COAD-US1160254899160254899single base substitutionCT5_prime_UTR_variant
COAD-US1160254899160254899single base substitutionCTupstream_gene_variant
COCA-CN1160183062160183062single base substitutionGAdownstream_gene_variant
COCA-CN1160209934160209934single base substitutionTCsynonymous_variantE246E738A>G
COCA-CN1160209934160209934single base substitutionTCsynonymous_variantE304E912A>G
COCA-CN1160249921160249921single base substitutionGTmissense_variantP107H320C>A
COCA-CN1160249921160249921single base substitutionGTmissense_variantP90H269C>A
ESAD-UK1160183632160183632single base substitutionCGdownstream_gene_variant
ESAD-UK1160185221160185221single base substitutionGAdownstream_gene_variant
ESAD-UK1160185304160185304single base substitutionCGdownstream_gene_variant
ESAD-UK1160186722160186722single base substitutionGAdownstream_gene_variant
ESAD-UK1160192779160192779single base substitutionCTintron_variant
ESAD-UK1160193613160193613single base substitutionGAintron_variant
ESAD-UK1160197387160197387single base substitutionCGintron_variant
ESAD-UK1160198272160198272single base substitutionCAintron_variant
ESAD-UK1160201408160201408single base substitutionAGintron_variant
ESAD-UK1160203834160203834single base substitutionGAintron_variant
ESAD-UK1160205438160205438single base substitutionCTdownstream_gene_variant
ESAD-UK1160205438160205438single base substitutionCTintron_variant
ESAD-UK1160210634160210634single base substitutionAGintron_variant
ESAD-UK1160212382160212382single base substitutionCGintron_variant
ESAD-UK1160214553160214553single base substitutionGAintron_variant
ESAD-UK1160216147160216147single base substitutionTGintron_variant
ESAD-UK1160218051160218051single base substitutionAGintron_variant
ESAD-UK1160218244160218244single base substitutionGCintron_variant
ESAD-UK1160219452160219452single base substitutionTGintron_variant
ESAD-UK1160220648160220648single base substitutionTAintron_variant
ESAD-UK1160220841160220841single base substitutionCTintron_variant
ESAD-UK1160222846160222846single base substitutionACintron_variant
ESAD-UK1160223565160223565single base substitutionGAintron_variant
ESAD-UK1160223667160223667deletion of <=200bpA-intron_variant
ESAD-UK1160230187160230187single base substitutionTCintron_variant
ESAD-UK1160232030160232030deletion of <=200bpG-intron_variant
ESAD-UK1160233392160233392single base substitutionCTintron_variant
ESAD-UK1160233850160233850insertion of <=200bp-Tintron_variant
ESAD-UK1160234638160234638single base substitutionGAintron_variant
ESAD-UK1160235739160235739single base substitutionCTintron_variant
ESAD-UK1160236167160236167single base substitutionCTintron_variant
ESAD-UK1160238664160238664single base substitutionCTintron_variant
ESAD-UK1160239198160239199deletion of <=200bpAT-intron_variant
ESAD-UK1160239198160239200deletion of <=200bpATT-intron_variant
ESAD-UK1160240329160240329single base substitutionGAintron_variant
ESAD-UK1160240755160240755insertion of <=200bp-Tintron_variant
ESAD-UK1160241696160241696single base substitutionTAintron_variant
ESAD-UK1160242477160242477single base substitutionTCintron_variant
ESAD-UK1160243557160243557single base substitutionCTintron_variant
ESAD-UK1160245252160245252single base substitutionCTintron_variant
ESAD-UK1160253141160253141single base substitutionAGintron_variant
ESAD-UK1160253141160253141single base substitutionAGupstream_gene_variant
ESAD-UK1160253160160253160single base substitutionACintron_variant
ESAD-UK1160253160160253160single base substitutionACupstream_gene_variant
ESAD-UK1160253413160253413single base substitutionGAintron_variant
ESAD-UK1160253413160253413single base substitutionGAupstream_gene_variant
ESAD-UK1160257262160257262single base substitutionCAupstream_gene_variant
ESAD-UK1160259265160259265single base substitutionCGupstream_gene_variant
ESCA-CN1160210105160210105single base substitutionTCsynonymous_variantT189T567A>G
ESCA-CN1160210105160210105single base substitutionTCsynonymous_variantT247T741A>G
GBM-US1160250017160250017single base substitutionCTmissense_variantS58N173G>A
GBM-US1160250017160250017single base substitutionCTmissense_variantS75N224G>A
GBM-US1160254853160254853single base substitutionAG5_prime_UTR_variant
GBM-US1160254853160254853single base substitutionAGupstream_gene_variant
KIRC-US1160209814160209814single base substitutionAGdownstream_gene_variant
KIRC-US1160209814160209814single base substitutionAGsynonymous_variantD286D858T>C
KIRP-US1160253370160253370single base substitutionCTintron_variant
KIRP-US1160253370160253370single base substitutionCTupstream_gene_variant
LAML-KR1160188807160188807single base substitutionGTintron_variant
LAML-KR1160219213160219213single base substitutionTCintron_variant
LAML-KR1160252696160252696single base substitutionTGintron_variant
LAML-KR1160252696160252696single base substitutionTGupstream_gene_variant
LGG-US1160209956160209956single base substitutionCAmissense_variantG239V716G>T
LGG-US1160209956160209956single base substitutionCAmissense_variantG297V890G>T
LICA-FR1160183232160183232insertion of <=200bp-TCCGGCAGCdownstream_gene_variant
LICA-FR1160198986160198986single base substitutionTCintron_variant
LICA-FR1160199003160199003single base substitutionTGintron_variant
LICA-FR1160252819160252819single base substitutionGC5_prime_UTR_premature_start_codon_gain_variant
LICA-FR1160252819160252819single base substitutionGCupstream_gene_variant
LICA-FR1160253234160253234single base substitutionCTintron_variant
LICA-FR1160253234160253234single base substitutionCTupstream_gene_variant
LINC-JP1160186808160186808single base substitutionATdownstream_gene_variant
LINC-JP1160187126160187126single base substitutionGTdownstream_gene_variant
LINC-JP1160188161160188161single base substitutionTCmissense_variantM698V2092A>G
LINC-JP1160189235160189235single base substitutionTCintron_variant
LINC-JP1160190637160190637single base substitutionGTintron_variant
LINC-JP1160202909160202909single base substitutionTCintron_variant
LINC-JP1160206292160206292deletion of <=200bpA-downstream_gene_variant
LINC-JP1160206292160206292deletion of <=200bpA-intron_variant
LINC-JP1160207100160207100single base substitutionAGdownstream_gene_variant
LINC-JP1160207100160207100single base substitutionAGintron_variant
LINC-JP1160209539160209539single base substitutionCTdownstream_gene_variant
LINC-JP1160209539160209539single base substitutionCTmissense_variantR378Q1133G>A
LINC-JP1160209899160209899single base substitutionTGdownstream_gene_variant
LINC-JP1160209899160209899single base substitutionTGmissense_variantE258A773A>C
LINC-JP1160218574160218574single base substitutionTAintron_variant
LINC-JP1160219043160219043single base substitutionTCintron_variant
LINC-JP1160236533160236533single base substitutionGCintron_variant
LINC-JP1160247630160247630single base substitutionTCintron_variant
LINC-JP1160247855160247855single base substitutionTAintron_variant
LINC-JP1160252662160252662single base substitutionACintron_variant
LINC-JP1160252662160252662single base substitutionACupstream_gene_variant
LINC-JP1160252879160252879single base substitutionTA5_prime_UTR_premature_start_codon_gain_variant
LINC-JP1160252879160252879single base substitutionTAupstream_gene_variant
LINC-JP1160257200160257200single base substitutionACupstream_gene_variant
LIRI-JP1160182959160182959single base substitutionAGdownstream_gene_variant
LIRI-JP1160185079160185079single base substitutionGTdownstream_gene_variant
LIRI-JP1160185179160185179single base substitutionTGdownstream_gene_variant
LIRI-JP1160185718160185718single base substitutionTCdownstream_gene_variant
LIRI-JP1160187546160187546single base substitutionACintron_variant
LIRI-JP1160187752160187752single base substitutionAGintron_variant
LIRI-JP1160194149160194149single base substitutionCGintron_variant
LIRI-JP1160194185160194185single base substitutionCTintron_variant
LIRI-JP1160195549160195549single base substitutionGAintron_variant
LIRI-JP1160195608160195608deletion of <=200bpC-intron_variant
LIRI-JP1160196400160196400single base substitutionTGintron_variant
LIRI-JP1160197649160197649single base substitutionTAintron_variant
LIRI-JP1160197689160197689single base substitutionTCintron_variant
LIRI-JP1160197762160197762single base substitutionGAintron_variant
LIRI-JP1160201876160201876single base substitutionGAintron_variant
LIRI-JP1160202079160202079single base substitutionTCintron_variant
LIRI-JP1160203858160203858single base substitutionGTintron_variant
LIRI-JP1160204055160204055single base substitutionGAintron_variant
LIRI-JP1160207638160207638single base substitutionTCdownstream_gene_variant
LIRI-JP1160207638160207638single base substitutionTCintron_variant
LIRI-JP1160212533160212533single base substitutionTAintron_variant
LIRI-JP1160212940160212940single base substitutionGCintron_variant
LIRI-JP1160215830160215830single base substitutionATintron_variant
LIRI-JP1160216097160216097single base substitutionCTintron_variant
LIRI-JP1160219125160219125single base substitutionACintron_variant
LIRI-JP1160219605160219605single base substitutionAGintron_variant
LIRI-JP1160221839160221840deletion of <=200bpAC-intron_variant
LIRI-JP1160227554160227554single base substitutionTGintron_variant
LIRI-JP1160229715160229715single base substitutionGAintron_variant
LIRI-JP1160231758160231758single base substitutionCAintron_variant
LIRI-JP1160231809160231809single base substitutionTGintron_variant
LIRI-JP1160232737160232737single base substitutionTGintron_variant
LIRI-JP1160233146160233146single base substitutionGTintron_variant
LIRI-JP1160233146160233146single base substitutionGTmissense_variantS198R594C>A
LIRI-JP1160233920160233920single base substitutionGAintron_variant
LIRI-JP1160235105160235105single base substitutionACintron_variant
LIRI-JP1160235650160235650single base substitutionTAintron_variant
LIRI-JP1160235727160235727single base substitutionCTintron_variant
LIRI-JP1160236593160236593single base substitutionAGintron_variant
LIRI-JP1160237622160237622single base substitutionACintron_variant
LIRI-JP1160240899160240899single base substitutionTGintron_variant
LIRI-JP1160244798160244798single base substitutionTCintron_variant
LIRI-JP1160245013160245013single base substitutionTCintron_variant
LIRI-JP1160247457160247457single base substitutionAGintron_variant
LIRI-JP1160247994160247997deletion of <=200bpTAAT-intron_variant
LIRI-JP1160249033160249033single base substitutionTCintron_variant
LIRI-JP1160250757160250757single base substitutionTCintron_variant
LIRI-JP1160251533160251533single base substitutionTCintron_variant
LIRI-JP1160253514160253514single base substitutionGTintron_variant
LIRI-JP1160253514160253514single base substitutionGTupstream_gene_variant
LIRI-JP1160254550160254550insertion of <=200bp-Tintron_variant
LIRI-JP1160254550160254550insertion of <=200bp-Tupstream_gene_variant
LIRI-JP1160255433160255433single base substitutionCAupstream_gene_variant
LIRI-JP1160257177160257177single base substitutionACupstream_gene_variant
LIRI-JP1160258641160258641insertion of <=200bp-Aupstream_gene_variant
LUSC-KR1160183051160183051single base substitutionCTdownstream_gene_variant
LUSC-KR1160194355160194355single base substitutionAGintron_variant
LUSC-KR1160207398160207398single base substitutionCAdownstream_gene_variant
LUSC-KR1160207398160207398single base substitutionCAintron_variant
LUSC-KR1160209860160209860single base substitutionCAdownstream_gene_variant
LUSC-KR1160209860160209860single base substitutionCAmissense_variantR271L812G>T
LUSC-KR1160211677160211677single base substitutionGAintron_variant
LUSC-KR1160218339160218339single base substitutionCAintron_variant
LUSC-KR1160220876160220876single base substitutionCGintron_variant
LUSC-KR1160220907160220907single base substitutionGCintron_variant
LUSC-KR1160225548160225548single base substitutionTCintron_variant
LUSC-KR1160231409160231409single base substitutionCGintron_variant
LUSC-KR1160233377160233377single base substitutionGCintron_variant
LUSC-KR1160233448160233448single base substitutionTCintron_variant
LUSC-KR1160236470160236470single base substitutionTAintron_variant
LUSC-KR1160242660160242660single base substitutionGAintron_variant
LUSC-KR1160248764160248764single base substitutionCGintron_variant
LUSC-KR1160249391160249391single base substitutionTAintron_variant
LUSC-KR1160249799160249799single base substitutionTAintron_variant
LUSC-KR1160251792160251792single base substitutionAGintron_variant
LUSC-KR1160257559160257559single base substitutionCGupstream_gene_variant
LUSC-US1160182942160182942single base substitutionGAdownstream_gene_variant
LUSC-US1160207000160207000single base substitutionGCdownstream_gene_variant
LUSC-US1160207000160207000single base substitutionGCmissense_variantS449C1346C>G
LUSC-US1160209596160209596single base substitutionCAdownstream_gene_variant
LUSC-US1160209596160209596single base substitutionCAmissense_variantG359V1076G>T
LUSC-US1160209783160209783single base substitutionCAdownstream_gene_variant
LUSC-US1160209783160209783single base substitutionCAstop_gainedE297*889G>T
LUSC-US1160252819160252819single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
LUSC-US1160252819160252819single base substitutionGAupstream_gene_variant
MALY-DE1160185389160185389single base substitutionAGdownstream_gene_variant
MALY-DE1160191619160191619single base substitutionACintron_variant
MALY-DE1160191632160191632single base substitutionAGintron_variant
MALY-DE1160194086160194086single base substitutionTCintron_variant
MALY-DE1160199514160199514single base substitutionATintron_variant
MALY-DE1160199520160199520single base substitutionATintron_variant
MALY-DE1160203267160203267single base substitutionCAintron_variant
MALY-DE1160216804160216804single base substitutionTCintron_variant
MALY-DE1160217227160217227single base substitutionGAintron_variant
MALY-DE1160227692160227692single base substitutionTAintron_variant
MALY-DE1160229483160229483insertion of <=200bp-Aintron_variant
MALY-DE1160230030160230030single base substitutionACintron_variant
MALY-DE1160230503160230503single base substitutionCGintron_variant
MALY-DE1160232501160232501single base substitutionTCintron_variant
MALY-DE1160232519160232519single base substitutionGCintron_variant
MALY-DE1160232529160232529single base substitutionAGintron_variant
MALY-DE1160233841160233841single base substitutionTCintron_variant
MALY-DE1160234986160234986single base substitutionTCintron_variant
MALY-DE1160239165160239165single base substitutionCGintron_variant
MALY-DE1160246316160246316single base substitutionGTintron_variant
MELA-AU1160183601160183601single base substitutionCTdownstream_gene_variant
MELA-AU1160183706160183706single base substitutionGAdownstream_gene_variant
MELA-AU1160184027160184027single base substitutionCTdownstream_gene_variant
MELA-AU1160185385160185385single base substitutionCTdownstream_gene_variant
MELA-AU1160187151160187151single base substitutionCTdownstream_gene_variant
MELA-AU1160187251160187251single base substitutionGAdownstream_gene_variant
MELA-AU1160188154160188154single base substitutionCTstop_gainedW700*2099G>A
MELA-AU1160188257160188257single base substitutionGAintron_variant
MELA-AU1160189523160189523single base substitutionAGintron_variant
MELA-AU1160190597160190597single base substitutionCTintron_variant
MELA-AU1160191467160191467single base substitutionCGintron_variant
MELA-AU1160192047160192047single base substitutionGAintron_variant
MELA-AU1160192077160192077single base substitutionGAintron_variant
MELA-AU1160192224160192224single base substitutionCTintron_variant
MELA-AU1160192442160192442single base substitutionACmissense_variantV634G1901T>G
MELA-AU1160192905160192905single base substitutionGAintron_variant
MELA-AU1160193058160193058single base substitutionGAintron_variant
MELA-AU1160193108160193108single base substitutionTCintron_variant
MELA-AU1160193477160193477single base substitutionCTintron_variant
MELA-AU1160193924160193924single base substitutionCTintron_variant
MELA-AU1160193942160193942single base substitutionGAintron_variant
MELA-AU1160194971160194971single base substitutionGAintron_variant
MELA-AU1160196101160196101single base substitutionCTintron_variant
MELA-AU1160196290160196290single base substitutionAGintron_variant
MELA-AU1160197137160197137single base substitutionCGintron_variant
MELA-AU1160197394160197394single base substitutionGAintron_variant
MELA-AU1160197903160197903single base substitutionGAintron_variant
MELA-AU1160198043160198043single base substitutionGAintron_variant
MELA-AU1160198361160198362multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1160198693160198693single base substitutionGTintron_variant
MELA-AU1160199041160199041single base substitutionGAintron_variant
MELA-AU1160199450160199450single base substitutionGAintron_variant
MELA-AU1160199680160199680single base substitutionGAintron_variant
MELA-AU1160199867160199867single base substitutionGAintron_variant
MELA-AU1160199884160199884single base substitutionGAintron_variant
MELA-AU1160199902160199902single base substitutionGAintron_variant
MELA-AU1160200986160200986single base substitutionGAintron_variant
MELA-AU1160201363160201363single base substitutionGAintron_variant
MELA-AU1160202597160202597single base substitutionGAintron_variant
MELA-AU1160202676160202676single base substitutionGAintron_variant
MELA-AU1160202894160202894single base substitutionGAintron_variant
MELA-AU1160203112160203112single base substitutionGAintron_variant
MELA-AU1160203842160203842single base substitutionGAintron_variant
MELA-AU1160204132160204132single base substitutionGAintron_variant
MELA-AU1160204558160204559multiple base substitution (>=2bp and <=200bp)AGGAintron_variant
MELA-AU1160204932160204932single base substitutionGTdownstream_gene_variant
MELA-AU1160204932160204932single base substitutionGTintron_variant
MELA-AU1160205041160205041single base substitutionAGdownstream_gene_variant
MELA-AU1160205041160205041single base substitutionAGintron_variant
MELA-AU1160205962160205962single base substitutionGAdownstream_gene_variant
MELA-AU1160205962160205962single base substitutionGAintron_variant
MELA-AU1160206007160206007single base substitutionCTdownstream_gene_variant
MELA-AU1160206007160206007single base substitutionCTintron_variant
MELA-AU1160206113160206113single base substitutionTCdownstream_gene_variant
MELA-AU1160206113160206113single base substitutionTCintron_variant
MELA-AU1160206337160206337single base substitutionGAdownstream_gene_variant
MELA-AU1160206337160206337single base substitutionGAintron_variant
MELA-AU1160206905160206905single base substitutionGAdownstream_gene_variant
MELA-AU1160206905160206905single base substitutionGAintron_variant
MELA-AU1160206997160206997single base substitutionGAdownstream_gene_variant
MELA-AU1160206997160206997single base substitutionGAmissense_variantP450L1349C>T
MELA-AU1160207165160207165single base substitutionGAdownstream_gene_variant
MELA-AU1160207165160207165single base substitutionGAintron_variant
MELA-AU1160208056160208056single base substitutionAGdownstream_gene_variant
MELA-AU1160208056160208056single base substitutionAGintron_variant
MELA-AU1160208889160208889single base substitutionGAdownstream_gene_variant
MELA-AU1160208889160208889single base substitutionGAintron_variant
MELA-AU1160209143160209143single base substitutionACdownstream_gene_variant
MELA-AU1160209143160209143single base substitutionACintron_variant
MELA-AU1160210194160210194single base substitutionGAintron_variant
MELA-AU1160210952160210952single base substitutionATintron_variant
MELA-AU1160211038160211038single base substitutionGAintron_variant
MELA-AU1160211283160211283single base substitutionTGintron_variant
MELA-AU1160211981160211981single base substitutionGAintron_variant
MELA-AU1160213544160213544single base substitutionGAintron_variant
MELA-AU1160214100160214100single base substitutionGAintron_variant
MELA-AU1160214213160214213single base substitutionGAintron_variant
MELA-AU1160215368160215368single base substitutionGAintron_variant
MELA-AU1160216230160216230single base substitutionGAintron_variant
MELA-AU1160216357160216357single base substitutionGAintron_variant
MELA-AU1160216660160216660single base substitutionGAintron_variant
MELA-AU1160216998160216998single base substitutionGAintron_variant
MELA-AU1160217175160217175single base substitutionCAintron_variant
MELA-AU1160218045160218045single base substitutionCTintron_variant
MELA-AU1160218447160218447single base substitutionCTintron_variant
MELA-AU1160218675160218675single base substitutionGAintron_variant
MELA-AU1160218873160218873single base substitutionGAintron_variant
MELA-AU1160219096160219096single base substitutionTAintron_variant
MELA-AU1160219638160219638single base substitutionGAintron_variant
MELA-AU1160220948160220948single base substitutionGAintron_variant
MELA-AU1160221220160221220single base substitutionCGintron_variant
MELA-AU1160221312160221312single base substitutionGAintron_variant
MELA-AU1160222255160222255single base substitutionGAintron_variant
MELA-AU1160222757160222757single base substitutionGAintron_variant
MELA-AU1160222867160222867single base substitutionGAintron_variant
MELA-AU1160222923160222923single base substitutionGAintron_variant
MELA-AU1160223373160223373single base substitutionGAintron_variant
MELA-AU1160224099160224099single base substitutionGAintron_variant
MELA-AU1160225028160225028single base substitutionCTintron_variant
MELA-AU1160225316160225316single base substitutionGAintron_variant
MELA-AU1160226001160226001single base substitutionGAintron_variant
MELA-AU1160228350160228350single base substitutionGAintron_variant
MELA-AU1160228361160228361single base substitutionGAintron_variant
MELA-AU1160228695160228695single base substitutionCGintron_variant
MELA-AU1160229126160229126single base substitutionCTintron_variant
MELA-AU1160229204160229204single base substitutionTCintron_variant
MELA-AU1160229217160229217single base substitutionGAintron_variant
MELA-AU1160229459160229459single base substitutionGAintron_variant
MELA-AU1160229612160229612single base substitutionAGintron_variant
MELA-AU1160230187160230187single base substitutionTCintron_variant
MELA-AU1160230197160230197single base substitutionTAintron_variant
MELA-AU1160231060160231060single base substitutionCTintron_variant
MELA-AU1160232404160232404single base substitutionGAintron_variant
MELA-AU1160232961160232961single base substitutionGAintron_variant
MELA-AU1160233444160233444single base substitutionCTintron_variant
MELA-AU1160233701160233701single base substitutionGAintron_variant
MELA-AU1160233790160233790single base substitutionATintron_variant
MELA-AU1160233810160233810single base substitutionCTintron_variant
MELA-AU1160233892160233892single base substitutionCTintron_variant
MELA-AU1160234204160234204single base substitutionGAintron_variant
MELA-AU1160234547160234547single base substitutionGAintron_variant
MELA-AU1160234854160234854single base substitutionCTintron_variant
MELA-AU1160234968160234968single base substitutionGAintron_variant
MELA-AU1160235521160235521single base substitutionGTintron_variant
MELA-AU1160235634160235634single base substitutionCTintron_variant
MELA-AU1160235848160235848single base substitutionGAintron_variant
MELA-AU1160235891160235891single base substitutionAGintron_variant
MELA-AU1160235976160235976single base substitutionCTintron_variant
MELA-AU1160236004160236004single base substitutionCTintron_variant
MELA-AU1160236021160236021single base substitutionCGintron_variant
MELA-AU1160236198160236198single base substitutionCTintron_variant
MELA-AU1160236230160236230single base substitutionGAintron_variant
MELA-AU1160236315160236315single base substitutionGAintron_variant
MELA-AU1160236344160236344single base substitutionCTintron_variant
MELA-AU1160236397160236397single base substitutionGAintron_variant
MELA-AU1160236952160236955deletion of <=200bpCCTG-intron_variant
MELA-AU1160237020160237020single base substitutionGAintron_variant
MELA-AU1160237095160237096multiple base substitution (>=2bp and <=200bp)GGACintron_variant
MELA-AU1160237942160237942single base substitutionGTintron_variant
MELA-AU1160238219160238219single base substitutionCTintron_variant
MELA-AU1160238847160238847single base substitutionGAintron_variant
MELA-AU1160239178160239178single base substitutionGAintron_variant
MELA-AU1160239427160239427single base substitutionCTintron_variant
MELA-AU1160239500160239500single base substitutionGAintron_variant
MELA-AU1160240100160240100single base substitutionTGintron_variant
MELA-AU1160240322160240322single base substitutionCTintron_variant
MELA-AU1160240522160240522single base substitutionCTintron_variant
MELA-AU1160240569160240569single base substitutionCTintron_variant
MELA-AU1160241099160241099single base substitutionGAintron_variant
MELA-AU1160241576160241577multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1160241679160241679single base substitutionGAintron_variant
MELA-AU1160241694160241694single base substitutionTAintron_variant
MELA-AU1160241773160241773single base substitutionCTintron_variant
MELA-AU1160242442160242442single base substitutionCTintron_variant
MELA-AU1160242701160242701single base substitutionGAintron_variant
MELA-AU1160243200160243200single base substitutionCTintron_variant
MELA-AU1160243690160243690single base substitutionGAintron_variant
MELA-AU1160244956160244956single base substitutionGAintron_variant
MELA-AU1160245482160245482single base substitutionGAintron_variant
MELA-AU1160245669160245669single base substitutionGAintron_variant
MELA-AU1160246156160246156single base substitutionGAintron_variant
MELA-AU1160246694160246694single base substitutionGAintron_variant
MELA-AU1160247096160247096single base substitutionGAintron_variant
MELA-AU1160247167160247167single base substitutionGAintron_variant
MELA-AU1160247516160247516single base substitutionGAintron_variant
MELA-AU1160248075160248075single base substitutionTCintron_variant
MELA-AU1160248614160248614single base substitutionGAintron_variant
MELA-AU1160248626160248626single base substitutionGAintron_variant
MELA-AU1160249067160249067single base substitutionGAintron_variant
MELA-AU1160249126160249126single base substitutionGAintron_variant
MELA-AU1160249313160249313single base substitutionGAintron_variant
MELA-AU1160249648160249648single base substitutionGAintron_variant
MELA-AU1160249655160249655single base substitutionGAintron_variant
MELA-AU1160249905160249905single base substitutionGAsynonymous_variantT112T336C>T
MELA-AU1160249905160249905single base substitutionGAsynonymous_variantT95T285C>T
MELA-AU1160250048160250048single base substitutionGAintron_variant
MELA-AU1160250062160250062single base substitutionAGintron_variant
MELA-AU1160250125160250125single base substitutionGAintron_variant
MELA-AU1160250131160250131single base substitutionGAintron_variant
MELA-AU1160251411160251411single base substitutionGAintron_variant
MELA-AU1160252765160252765single base substitutionGA5_prime_UTR_variant
MELA-AU1160252765160252765single base substitutionGAupstream_gene_variant
MELA-AU1160252906160252906single base substitutionGAsplice_region_variant
MELA-AU1160252906160252906single base substitutionGAupstream_gene_variant
MELA-AU1160253076160253076single base substitutionGAintron_variant
MELA-AU1160253076160253076single base substitutionGAupstream_gene_variant
MELA-AU1160253210160253210single base substitutionGAintron_variant
MELA-AU1160253210160253210single base substitutionGAupstream_gene_variant
MELA-AU1160253513160253514multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1160253513160253514multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU1160254384160254384single base substitutionGAintron_variant
MELA-AU1160254384160254384single base substitutionGAupstream_gene_variant
MELA-AU1160254926160254926single base substitutionCTupstream_gene_variant
MELA-AU1160254939160254939single base substitutionGAupstream_gene_variant
MELA-AU1160254946160254946single base substitutionGAupstream_gene_variant
MELA-AU1160254948160254948single base substitutionCTupstream_gene_variant
MELA-AU1160254969160254969single base substitutionCTupstream_gene_variant
MELA-AU1160254971160254971single base substitutionCTupstream_gene_variant
MELA-AU1160254980160254980single base substitutionCTupstream_gene_variant
MELA-AU1160254984160254984single base substitutionCTupstream_gene_variant
MELA-AU1160254995160254995single base substitutionCTupstream_gene_variant
MELA-AU1160255172160255172single base substitutionAGupstream_gene_variant
MELA-AU1160255652160255652single base substitutionCTupstream_gene_variant
MELA-AU1160256393160256393single base substitutionATupstream_gene_variant
MELA-AU1160256695160256695single base substitutionAGupstream_gene_variant
MELA-AU1160257334160257334single base substitutionTGupstream_gene_variant
MELA-AU1160257563160257563single base substitutionGAupstream_gene_variant
MELA-AU1160258242160258242single base substitutionGAupstream_gene_variant
MELA-AU1160258891160258891single base substitutionCTupstream_gene_variant
MELA-AU1160259331160259331single base substitutionGAupstream_gene_variant
MELA-AU1160259429160259429single base substitutionGAupstream_gene_variant
ORCA-IN1160206803160206803single base substitutionCTdownstream_gene_variant
ORCA-IN1160206803160206803single base substitutionCTintron_variant
ORCA-IN1160217974160217974single base substitutionGAintron_variant
ORCA-IN1160223517160223517single base substitutionGAintron_variant
ORCA-IN1160251637160251637single base substitutionCAintron_variant
OV-AU1160184552160184552single base substitutionGTdownstream_gene_variant
OV-AU1160187952160187952single base substitutionGAintron_variant
OV-AU1160199744160199744single base substitutionCTintron_variant
OV-AU1160210663160210663single base substitutionGTintron_variant
OV-AU1160212334160212334single base substitutionGAintron_variant
OV-AU1160213893160213893single base substitutionGAintron_variant
OV-AU1160221784160221784single base substitutionCTintron_variant
OV-AU1160223311160223311single base substitutionGAintron_variant
OV-AU1160225952160225952single base substitutionTGintron_variant
OV-AU1160226845160226845single base substitutionCTintron_variant
OV-AU1160235756160235756single base substitutionCGintron_variant
OV-AU1160244711160244711single base substitutionTCintron_variant
OV-AU1160254974160254974single base substitutionCGupstream_gene_variant
OV-AU1160259278160259278single base substitutionAGupstream_gene_variant
OV-AU1160259352160259352single base substitutionTCupstream_gene_variant
OV-US1160236616160236616single base substitutionGCintron_variant
PACA-AU1160183045160183045single base substitutionGTdownstream_gene_variant
PACA-AU1160185118160185118single base substitutionCTdownstream_gene_variant
PACA-AU1160189882160189885deletion of <=200bpAAAC-intron_variant
PACA-AU1160197266160197266single base substitutionCTintron_variant
PACA-AU1160198497160198497single base substitutionAGintron_variant
PACA-AU1160199673160199673single base substitutionCTintron_variant
PACA-AU1160203086160203086single base substitutionCTintron_variant
PACA-AU1160206232160206232single base substitutionGAdownstream_gene_variant
PACA-AU1160206232160206232single base substitutionGAintron_variant
PACA-AU1160206234160206234single base substitutionGAdownstream_gene_variant
PACA-AU1160206234160206234single base substitutionGAintron_variant
PACA-AU1160206236160206236single base substitutionGAdownstream_gene_variant
PACA-AU1160206236160206236single base substitutionGAintron_variant
PACA-AU1160212325160212325single base substitutionAGintron_variant
PACA-AU1160213214160213214single base substitutionTAintron_variant
PACA-AU1160224947160224947single base substitutionCTintron_variant
PACA-AU1160235339160235339single base substitutionCGintron_variant
PACA-AU1160236896160236896single base substitutionTAintron_variant
PACA-AU1160242730160242730single base substitutionGCintron_variant
PACA-AU1160244966160244966single base substitutionCGintron_variant
PACA-AU1160246289160246289single base substitutionATintron_variant
PACA-AU1160246357160246357single base substitutionAGintron_variant
PACA-AU1160249735160249736deletion of <=200bpGA-intron_variant
PACA-AU1160252347160252347single base substitutionCAintron_variant
PACA-AU1160252347160252347single base substitutionCAupstream_gene_variant
PACA-AU1160256574160256574single base substitutionTCupstream_gene_variant
PACA-CA1160183302160183302single base substitutionTCdownstream_gene_variant
PACA-CA1160186018160186018single base substitutionGCdownstream_gene_variant
PACA-CA1160186890160186890deletion of <=200bpG-downstream_gene_variant
PACA-CA1160186937160186937single base substitutionAGdownstream_gene_variant
PACA-CA1160189182160189182single base substitutionGCintron_variant
PACA-CA1160203198160203198insertion of <=200bp-Aintron_variant
PACA-CA1160203771160203771single base substitutionGTintron_variant
PACA-CA1160204165160204165single base substitutionGCintron_variant
PACA-CA1160204309160204309single base substitutionGTintron_variant
PACA-CA1160206247160206247single base substitutionTCdownstream_gene_variant
PACA-CA1160206247160206247single base substitutionTCintron_variant
PACA-CA1160208971160208971single base substitutionGAdownstream_gene_variant
PACA-CA1160208971160208971single base substitutionGAintron_variant
PACA-CA1160209659160209659single base substitutionCTdownstream_gene_variant
PACA-CA1160209659160209659single base substitutionCTmissense_variantR338H1013G>A
PACA-CA1160209896160209896single base substitutionTCdownstream_gene_variant
PACA-CA1160209896160209896single base substitutionTCmissense_variantE259G776A>G
PACA-CA1160210879160210879single base substitutionTGintron_variant
PACA-CA1160214885160214885single base substitutionCGintron_variant
PACA-CA1160222723160222723single base substitutionGAintron_variant
PACA-CA1160225406160225406deletion of <=200bpG-intron_variant
PACA-CA1160230741160230741single base substitutionGCintron_variant
PACA-CA1160230935160230935single base substitutionACintron_variant
PACA-CA1160231132160231132single base substitutionGAintron_variant
PACA-CA1160237124160237124single base substitutionGCintron_variant
PACA-CA1160237653160237653single base substitutionCGintron_variant
PACA-CA1160238771160238771single base substitutionGAintron_variant
PACA-CA1160242481160242481single base substitutionCTintron_variant
PACA-CA1160243075160243075single base substitutionCTintron_variant
PACA-CA1160244693160244693single base substitutionATintron_variant
PACA-CA1160244789160244789single base substitutionGAintron_variant
PACA-CA1160244828160244828single base substitutionCTintron_variant
PACA-CA1160246929160246929single base substitutionATintron_variant
PACA-CA1160247369160247369single base substitutionCAintron_variant
PACA-CA1160249475160249475single base substitutionCTintron_variant
PACA-CA1160250005160250005single base substitutionGCmissense_variantS62C185C>G
PACA-CA1160250005160250005single base substitutionGCmissense_variantS79C236C>G
PACA-CA1160250315160250315single base substitutionCTintron_variant
PACA-CA1160256483160256483single base substitutionCGupstream_gene_variant
PACA-CA1160258581160258581single base substitutionTCupstream_gene_variant
PAEN-AU1160191801160191801single base substitutionAGintron_variant
PAEN-AU1160196576160196576single base substitutionTAintron_variant
PAEN-AU1160203274160203274single base substitutionTCintron_variant
PAEN-IT1160199012160199012single base substitutionGTintron_variant
PAEN-IT1160235625160235625single base substitutionCAintron_variant
PAEN-IT1160258240160258240single base substitutionGAupstream_gene_variant
PBCA-DE1160198878160198878single base substitutionAGintron_variant
PBCA-DE1160203669160203669single base substitutionCAintron_variant
PBCA-DE1160206237160206238deletion of <=200bpTA-downstream_gene_variant
PBCA-DE1160206237160206238deletion of <=200bpTA-intron_variant
PBCA-DE1160239189160239189insertion of <=200bp-Aintron_variant
PBCA-DE1160239199160239199deletion of <=200bpT-intron_variant
PBCA-DE1160240673160240674deletion of <=200bpAT-intron_variant
PBCA-DE1160258243160258244deletion of <=200bpTA-upstream_gene_variant
PRAD-CA1160213043160213043single base substitutionCAintron_variant
PRAD-UK1160184707160184707single base substitutionAGdownstream_gene_variant
PRAD-UK1160188781160188781single base substitutionAGintron_variant
PRAD-UK1160215840160215840single base substitutionATintron_variant
PRAD-UK1160218797160218797single base substitutionCAintron_variant
PRAD-UK1160226249160226249single base substitutionCGintron_variant
PRAD-US1160187426160187426single base substitutionCTmissense_variantD738N2212G>A
READ-US1160206934160206934single base substitutionCTdownstream_gene_variant
READ-US1160206934160206934single base substitutionCTmissense_variantR471H1412G>A
READ-US1160253413160253413single base substitutionGAintron_variant
READ-US1160253413160253413single base substitutionGAupstream_gene_variant
RECA-EU1160187495160187495single base substitutionATmissense_variantW715R2143T>A
RECA-EU1160198868160198868single base substitutionTAintron_variant
RECA-EU1160207797160207797single base substitutionCTdownstream_gene_variant
RECA-EU1160207797160207797single base substitutionCTintron_variant
RECA-EU1160209091160209091single base substitutionCAdownstream_gene_variant
RECA-EU1160209091160209091single base substitutionCAintron_variant
RECA-EU1160215446160215446single base substitutionTCintron_variant
RECA-EU1160221526160221526single base substitutionTGintron_variant
RECA-EU1160225293160225293single base substitutionATintron_variant
RECA-EU1160231188160231188single base substitutionCAintron_variant
RECA-EU1160243203160243203single base substitutionAGintron_variant
RECA-EU1160243328160243328single base substitutionCGintron_variant
SKCA-BR1160197144160197144single base substitutionTCintron_variant
SKCA-BR1160201832160201832single base substitutionTAintron_variant
SKCA-BR1160206887160206887single base substitutionGAdownstream_gene_variant
SKCA-BR1160206887160206887single base substitutionGAintron_variant
SKCA-BR1160211126160211126single base substitutionTGintron_variant
SKCA-BR1160214100160214100single base substitutionGAintron_variant
SKCA-BR1160215127160215127single base substitutionGAintron_variant
SKCA-BR1160216303160216303single base substitutionTAintron_variant
SKCA-BR1160217515160217515single base substitutionCGintron_variant
SKCA-BR1160218685160218685insertion of <=200bp-CAintron_variant
SKCA-BR1160223341160223341single base substitutionGAintron_variant
SKCA-BR1160223342160223342single base substitutionGAintron_variant
SKCA-BR1160223973160223973single base substitutionAGintron_variant
SKCA-BR1160226487160226487single base substitutionGTintron_variant
SKCA-BR1160230361160230361single base substitutionAGintron_variant
SKCA-BR1160232089160232089single base substitutionTGintron_variant
SKCA-BR1160232676160232676single base substitutionGAintron_variant
SKCA-BR1160233294160233294single base substitutionTGintron_variant
SKCA-BR1160240531160240531single base substitutionCTintron_variant
SKCA-BR1160241677160241677single base substitutionGAintron_variant
SKCA-BR1160241679160241679single base substitutionGAintron_variant
SKCA-BR1160241694160241694single base substitutionTAintron_variant
SKCA-BR1160247185160247185single base substitutionGCintron_variant
SKCA-BR1160253377160253377single base substitutionGAintron_variant
SKCA-BR1160253377160253377single base substitutionGAupstream_gene_variant
SKCA-BR1160253395160253395single base substitutionGAintron_variant
SKCA-BR1160253395160253395single base substitutionGAupstream_gene_variant
SKCA-BR1160257898160257898insertion of <=200bp-ATupstream_gene_variant
SKCM-US1160194883160194883single base substitutionGAsynonymous_variantI544I1632C>T
SKCM-US1160209930160209930single base substitutionGAdownstream_gene_variant
SKCM-US1160209930160209930single base substitutionGAstop_gainedR248*742C>T
SKCM-US1160250033160250033single base substitutionGAmissense_variantP53S157C>T
SKCM-US1160250033160250033single base substitutionGAmissense_variantP70S208C>T
SKCM-US1160252837160252837single base substitutionGA5_prime_UTR_variant
SKCM-US1160252837160252837single base substitutionGAupstream_gene_variant
SKCM-US1160252888160252888single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
SKCM-US1160252888160252888single base substitutionGAupstream_gene_variant
SKCM-US1160253385160253385single base substitutionGAintron_variant
SKCM-US1160253385160253385single base substitutionGAupstream_gene_variant
SKCM-US1160254895160254895single base substitutionCT5_prime_UTR_variant
SKCM-US1160254895160254895single base substitutionCTupstream_gene_variant
STAD-US1160187442160187442single base substitutionGAsynonymous_variantS732S2196C>T
STAD-US1160188206160188206single base substitutionGAmissense_variantR683W2047C>T
STAD-US1160208501160208501single base substitutionCTdownstream_gene_variant
STAD-US1160208501160208501single base substitutionCTmissense_variantA408T1222G>A
STAD-US1160209863160209863single base substitutionCTdownstream_gene_variant
STAD-US1160209863160209863single base substitutionCTmissense_variantR270H809G>A
STAD-US1160249918160249918single base substitutionGAmissense_variantT108I323C>T
STAD-US1160249918160249918single base substitutionGAmissense_variantT91I272C>T
STAD-US1160251955160251955single base substitutionGTsynonymous_variantA26A78C>A
STAD-US1160251955160251955single base substitutionGTsynonymous_variantA9A27C>A
STAD-US1160252819160252819single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
STAD-US1160252819160252819single base substitutionGAupstream_gene_variant
STAD-US1160252825160252825single base substitutionCT5_prime_UTR_variant
STAD-US1160252825160252825single base substitutionCTupstream_gene_variant
STAD-US1160253356160253356single base substitutionCTintron_variant
STAD-US1160253356160253356single base substitutionCTupstream_gene_variant
THCA-SA1160206953160206953single base substitutionTCdownstream_gene_variant
THCA-SA1160206953160206953single base substitutionTCmissense_variantI465V1393A>G
UCEC-US1160183029160183029single base substitutionGAdownstream_gene_variant
UCEC-US1160183220160183220single base substitutionCTdownstream_gene_variant
UCEC-US1160188740160188740single base substitutionGTmissense_variantH641N1921C>A
UCEC-US1160194851160194851single base substitutionCTsplice_donor_variant
UCEC-US1160195426160195426single base substitutionCAmissense_variantE520D1560G>T
UCEC-US1160206928160206928single base substitutionGAdownstream_gene_variant
UCEC-US1160206928160206928single base substitutionGAmissense_variantA473V1418C>T
UCEC-US1160209667160209667single base substitutionCTdownstream_gene_variant
UCEC-US1160209667160209667single base substitutionCTsynonymous_variantQ335Q1005G>A
UCEC-US1160209729160209729single base substitutionGAdownstream_gene_variant
UCEC-US1160209729160209729single base substitutionGAmissense_variantR315W943C>T
UCEC-US1160209745160209745single base substitutionGTdownstream_gene_variant
UCEC-US1160209745160209745single base substitutionGTsynonymous_variantL309L927C>A
UCEC-US1160209761160209761single base substitutionGTdownstream_gene_variant
UCEC-US1160209761160209761single base substitutionGTmissense_variantP304H911C>A
UCEC-US1160209773160209773single base substitutionGAdownstream_gene_variant
UCEC-US1160209773160209773single base substitutionGAmissense_variantA300V899C>T
UCEC-US1160209861160209861single base substitutionGAdownstream_gene_variant
UCEC-US1160209861160209861single base substitutionGAmissense_variantR271C811C>T
UCEC-US1160209896160209907deletion of <=200bpTCCTCTTCCTCT-disruptive_inframe_deletionEEEEE255E
UCEC-US1160209896160209907deletion of <=200bpTCCTCTTCCTCT-downstream_gene_variant
UCEC-US1160210070160210070single base substitutionCTmissense_variantS201N602G>A
UCEC-US1160210070160210070single base substitutionCTmissense_variantS259N776G>A
UCEC-US1160213760160213760single base substitutionGAintron_variant
UCEC-US1160213760160213760single base substitutionGAsynonymous_variantD167D501C>T
UCEC-US1160213774160213774single base substitutionCTintron_variant
UCEC-US1160213774160213774single base substitutionCTmissense_variantD163N487G>A
UCEC-US1160249616160249616single base substitutionGTmissense_variantP117H350C>A
UCEC-US1160249616160249616single base substitutionGTmissense_variantP134H401C>A
UCEC-US1160249891160249891single base substitutionCTmissense_variantR100H299G>A
UCEC-US1160249891160249891single base substitutionCTmissense_variantR117H350G>A
UCEC-US1160249982160249982single base substitutionTGmissense_variantK70Q208A>C
UCEC-US1160249982160249982single base substitutionTGmissense_variantK87Q259A>C
UCEC-US1160252796160252796single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
UCEC-US1160252796160252796single base substitutionGAupstream_gene_variant
UCEC-US1160252819160252819single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
UCEC-US1160252819160252819single base substitutionGAupstream_gene_variant
UCEC-US1160252884160252884single base substitutionAC5_prime_UTR_premature_start_codon_gain_variant
UCEC-US1160252884160252884single base substitutionACupstream_gene_variant
UCEC-US1160253319160253319single base substitutionCAintron_variant
UCEC-US1160253319160253319single base substitutionCAupstream_gene_variant
UCEC-US1160253338160253338single base substitutionCTintron_variant
UCEC-US1160253338160253338single base substitutionCTupstream_gene_variant
UCEC-US1160253339160253339single base substitutionGAintron_variant
UCEC-US1160253339160253339single base substitutionGAupstream_gene_variant
UCEC-US1160253413160253413single base substitutionGAintron_variant
UCEC-US1160253413160253413single base substitutionGAupstream_gene_variant
UCEC-US1160254895160254895single base substitutionCT5_prime_UTR_variant
UCEC-US1160254895160254895single base substitutionCTupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
1946219COSM1578251c.333A>Tp.L111LSubstitution - coding silent1:160279843-160279843-
TCGA-A1-A0SD-01COSM1472864c.564G>Ap.E188ESubstitution - coding silent1:160240318-160240318-
PTC_405COSM5958495c.1393A>Gp.I465VSubstitution - Missense1:160237163-160237163-
587222COSM1203076c.1590C>Ap.F530LSubstitution - Missense1:160225606-160225606-
SC_9047COSM5553807c.707A>Cp.E236ASubstitution - Missense1:160240175-160240175-
TCGA-B5-A0JY-01COSM1583596c.1418C>Tp.A473VSubstitution - Missense1:160237138-160237138-
TCGA-06-0939COSM2152428c.173G>Ap.S58NSubstitution - Missense1:160280227-160280227-
CSCC-27-TCOSM1335480c.927C>Tp.L309LSubstitution - coding silent1:160239955-160239955-
587350COSM1203080c.1502T>Cp.F501SSubstitution - Missense1:160231327-160231327-
TCGA-CD-A4MG-01COSM4024122c.272C>Tp.T91ISubstitution - Missense1:160280128-160280128-
pfg008TCOSM1639578c.1073G>Ap.R358HSubstitution - Missense1:160239809-160239809-
TCGA-E2-A15I-01COSM3802474c.1137G>Cp.R379RSubstitution - coding silent1:160239745-160239745-
TCGA-22-4595-01COSM1145997c.889G>Tp.E297*Substitution - Nonsense1:160239993-160239993-
TCGA-BR-8078-01COSM4024120c.809G>Ap.R270HSubstitution - Missense1:160240073-160240073-
TCGA-BR-6452-01COSM4024114c.2196C>Tp.S732SSubstitution - coding silent1:160217652-160217652-
HCC156COSM3705161c.1133G>Ap.R378QSubstitution - Missense1:160239749-160239749-
TCGA-AP-A051-01COSM1583593c.927C>Ap.L309LSubstitution - coding silent1:160239955-160239955-
TCGA-B5-A0JY-01COSM1583588c.487G>Ap.D163NSubstitution - Missense1:160243984-160243984-
TCGA-BR-7851-01COSM4024116c.2047C>Tp.R683WSubstitution - Missense1:160218416-160218416-
TCGA-DR-A0ZM-01COSM1134406c.2147G>Tp.R716LSubstitution - Missense1:160217701-160217701-
CSCC-40-TCOSM4482895c.726C>Tp.S242SSubstitution - coding silent1:160240156-160240156-
Gp2DCOSM2085385c.2172C>Tp.D724DSubstitution - coding silent1:160217676-160217676-
CSCC-31-TCOSM4464443c.1796C>Tp.P599LSubstitution - Missense1:160222757-160222757-
TCGA-EE-A29Q-06COSM3476802c.742C>Tp.R248*Substitution - Nonsense1:160240140-160240140-
HT115COSM2085470c.228C>Tp.S76SSubstitution - coding silent1:160280172-160280172-
TCGA-AP-A059-01COSM1583590c.602G>Ap.S201NSubstitution - Missense1:160240280-160240280-
NCI-H835COSM2085423c.1162G>Tp.G388CSubstitution - Missense1:160239720-160239720-
TCGA-AX-A0J1-01COSM1583589c.501C>Tp.D167DSubstitution - coding silent1:160243970-160243970-
2_RESISTANTCOSM1721792c.52G>Ap.G18RSubstitution - Missense1:160282140-160282140-
TCGA-CG-4306-01COSM4024124c.27C>Ap.A9ASubstitution - coding silent1:160282165-160282165-
TCGA-AC-A23H-01COSM3802478c.499G>Cp.D167HSubstitution - Missense1:160243972-160243972-
TCGA-EE-A182-06COSM3476800c.1632C>Tp.I544ISubstitution - coding silent1:160225093-160225093-
TCGA-D1-A15V-01COSM1583586c.299G>Ap.R100HSubstitution - Missense1:160280101-160280101-
TCGA-AP-A059-01COSM1583595c.1005G>Ap.Q335QSubstitution - coding silent1:160239877-160239877-
TCGA-AX-A0J0-01COSM1583592c.899C>Tp.A300VSubstitution - Missense1:160239983-160239983-
CSCC-27-TCOSM4507933c.319C>Tp.L107FSubstitution - Missense1:160280081-160280081-
TCGA-39-5036-01COSM1145996c.1076G>Tp.G359VSubstitution - Missense1:160239806-160239806-
TCGA-BS-A0UA-01COSM1583594c.943C>Tp.R315WSubstitution - Missense1:160239939-160239939-
TCGA-A5-A0R8-01COSM1583591c.765_776del12p.E263_E266delEEEEDeletion - In frame1:160240106-160240117-
CSCC-60-TCOSM4531050c.2215G>Ap.E739KSubstitution - Missense1:160217633-160217633-
TCGA-AP-A059-01COSM1583587c.350C>Ap.P117HSubstitution - Missense1:160279826-160279826-
TCGA-ER-A19F-06COSM3476804c.157C>Tp.P53SSubstitution - Missense1:160280243-160280243-
TCGA-34-5231-01COSM1145995c.1346C>Gp.S449CSubstitution - Missense1:160237210-160237210-
PC-9BRc1COSM1685060c.125A>Gp.Y42CSubstitution - Missense1:160282067-160282067-
PCSI_0083_Pa_PCOSM3376804c.1013G>Ap.R338HSubstitution - Missense1:160239869-160239869-
TCGA-CW-5581-01COSM1134745c.1616A>Gp.E539GSubstitution - Missense1:160225109-160225109-
TCGA-A5-A0GH-01COSM1151875c.911C>Ap.P304HSubstitution - Missense1:160239971-160239971-
PCSI_0083_Pa_XCOSM3376804c.1013G>Ap.R338HSubstitution - Missense1:160239869-160239869-
ATL085COSM5704974c.1493C>Tp.T498ISubstitution - Missense1:160231336-160231336-
TCGA-EA-A439-01COSM4843669c.2198C>Tp.S733FSubstitution - Missense1:160217650-160217650-
TCGA-F5-6814-01COSM2085417c.1412G>Ap.R471HSubstitution - Missense1:160237144-160237144-
HCC156TCOSM3705161c.1133G>Ap.R378QSubstitution - Missense1:160239749-160239749-
Pat_14_BCOSM5844167c.1198C>Tp.P400SSubstitution - Missense1:160238735-160238735-
ODG9COSM5731293c.1790A>Gp.Y597CSubstitution - Missense1:160222763-160222763-
TCGA-D8-A27V-01COSM3802472c.1564G>Cp.E522QSubstitution - Missense1:160225632-160225632-
SH-4885COSM5018601c.1239C>Tp.D413DSubstitution - coding silent1:160238694-160238694-
ESO-0015COSM1249751c.1235G>Ap.R412HSubstitution - Missense1:160238698-160238698-
19COSM5745736c.1750G>Tp.G584CSubstitution - Missense1:160224463-160224463-
PD24209aCOSM5798352c.1533-10C>Gp.?Unknown1:160225673-160225673-
C0041TCOSM4140895c.2143T>Ap.W715RSubstitution - Missense1:160217705-160217705-
CSCC-19-TCOSM4550216c.54G>Ap.G18GSubstitution - coding silent1:160282138-160282138-
Gp5DCOSM2085383c.2185G>Ap.E729KSubstitution - Missense1:160217663-160217663-
CSCC-60-TCOSM4566781c.933_934CC>TTp.L312FSubstitution - Missense1:160239948-160239949-
TCGA-BH-A0HF-01COSM3802476c.821G>Ap.R274HSubstitution - Missense1:160240061-160240061-
587234COSM1203082c.1780G>Ap.V594ISubstitution - Missense1:160222773-160222773-
TCGA-BS-A0UV-01COSM1583597c.1560G>Tp.E520DSubstitution - Missense1:160225636-160225636-
PCSI_0083_Pa_P_526COSM3376804c.1013G>Ap.R338HSubstitution - Missense1:160239869-160239869-
TCGA-CJ-4882-01COSM1134746c.858T>Cp.D286DSubstitution - coding silent1:160240024-160240024-
ATL071COSM5704976c.58G>Tp.G20WSubstitution - Missense1:160282134-160282134-
HCC94COSM1601105c.2092A>Gp.M698VSubstitution - Missense1:160218371-160218371-
2_PRE-TREATMENTCOSM1721792c.52G>Ap.G18RSubstitution - Missense1:160282140-160282140-
ESO-147COSM1249753c.1862G>Ap.C621YSubstitution - Missense1:160222691-160222691-
CSCC-29-TCOSM4571335c.895T>Cp.S299PSubstitution - Missense1:160239987-160239987-
TCGA-FJ-A3ZE-01COSM3788930c.859G>Tp.E287*Substitution - Nonsense1:160240023-160240023-
TCGA-A6-5661-01COSM1335478c.1509G>Ap.V503VSubstitution - coding silent1:160231320-160231320-
Gp2DCOSM2085383c.2185G>Ap.E729KSubstitution - Missense1:160217663-160217663-
HCC94TCOSM1601105c.2092A>Gp.M698VSubstitution - Missense1:160218371-160218371-
HCT15COSM2085415c.1416A>Gp.P472PSubstitution - coding silent1:160237140-160237140-
TCGA-D5-6928-01COSM3687763c.6G>Ap.S2SSubstitution - coding silent1:160282186-160282186-
HCT116COSM2085417c.1412G>Ap.R471HSubstitution - Missense1:160237144-160237144-
S02322COSM5691079c.970G>Cp.V324LSubstitution - Missense1:160239912-160239912-
Pat_53_BCOSM5844169c.1099G>Ap.D367NSubstitution - Missense1:160239783-160239783-
YUFERYCOSM5378146c.145A>Cp.T49PSubstitution - Missense1:160282047-160282047-
TCGA-BS-A0UJ-01COSM1583585c.208A>Cp.K70QSubstitution - Missense1:160280192-160280192-
TCGA-06-0939-01COSM2152428c.173G>Ap.S58NSubstitution - Missense1:160280227-160280227-
LIM2099COSM4641015c.677C>Tp.S226LSubstitution - Missense1:160240205-160240205-
TCGA-AX-A0J1-01COSM1583598c.1663+1G>Ap.?Unknown1:160225061-160225061-
BN24TCOSM1601107c.773A>Cp.E258ASubstitution - Missense1:160240109-160240109-
TCGA-AB-2895-03COSM1317643c.676T>Cp.S226PSubstitution - Missense1:160240206-160240206-
TCGA-BR-6566-01COSM4024118c.1222G>Ap.A408TSubstitution - Missense1:160238711-160238711-
TCGA-HC-7817-01COSM3671464c.2212G>Ap.D738NSubstitution - Missense1:160217636-160217636-
NPC15FCOSM4995303c.1117G>Ap.V373MSubstitution - Missense1:160239765-160239765-
35MCOSM5580780c.913C>Tp.R305CSubstitution - Missense1:160239969-160239969-
Gp5DCOSM2085385c.2172C>Tp.D724DSubstitution - coding silent1:160217676-160217676-
N-Thy004COSM5095393c.569C>Tp.S190FSubstitution - Missense1:160240313-160240313-
BN24COSM1601107c.773A>Cp.E258ASubstitution - Missense1:160240109-160240109-
CRC-06TCOSM5456143c.269C>Ap.P90HSubstitution - Missense1:160280131-160280131-
TCGA-B5-A0K6-01COSM1151876c.811C>Tp.R271CSubstitution - Missense1:160240071-160240071-
77COSM5013965c.1957G>Cp.D653HSubstitution - Missense1:160218914-160218914-
TCGA-P5-A5EZ-01COSM4420585c.716G>Tp.G239VSubstitution - Missense1:160240166-160240166-
sysucc-1370TCOSM5469672c.738A>Gp.E246ESubstitution - coding silent1:160240144-160240144-
TCGA-AO-A0JE-01COSM1472865c.22A>Gp.K8ESubstitution - Missense1:160282170-160282170-
DU-145COSM1203082c.1780G>Ap.V594ISubstitution - Missense1:160222773-160222773-
TCGA-AP-A059-01COSM1583599c.1921C>Ap.H641NSubstitution - Missense1:160218950-160218950-
TCGA-D5-6928-01COSM1335476c.2162G>Tp.G721VSubstitution - Missense1:160217686-160217686-
DLD1COSM2085415c.1416A>Gp.P472PSubstitution - coding silent1:160237140-160237140-
ESCC-110TCOSM3934181c.567A>Gp.T189TSubstitution - coding silent1:160240315-160240315-
pfg008TCOSM1639578c.1073G>Ap.R358HSubstitution - Missense1:160239809-160239809-
587234COSM1203084c.1075G>Ap.G359SSubstitution - Missense1:160239807-160239807-
587332COSM1203078c.635A>Gp.N212SSubstitution - Missense1:160240247-160240247-
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.I81Tc.242T>C1160249948HNSC
AGMissensep.S226Pc.676T>C1160209996AML
CAMissensep.G359Vc.1076G>T1160209596LUSC
CAMissensep.R331Ic.992G>T1160209680SCLC
CAMissensep.R713Lc.2138G>T1160188115LUAD
CAMissensep.R713Lc.2138G>T1160188115STAD
CANonsensep.E297*c.889G>T1160209783LUSC
CANonsensep.E4*c.10G>T1160251972SCLC
CGMissensep.E256Qc.766G>C1160209906HNSC
CGMissensep.G220Ac.659G>C1160210013COREAD
CTMissensep.C621Yc.1862G>A1160192481ESCA
CTMissensep.D738Nc.2212G>A1160187426PRAD
CTMissensep.E217Kc.649G>A1160210023LUAD
CTMissensep.R100Hc.299G>A1160249891UCEC
CTMissensep.R358Hc.1073G>A1160209599STAD
CTMissensep.R412Hc.1235G>A1160208488ESCA
CTMissensep.S58Nc.173G>A1160250017GBM
CTMissensep.V634Mc.1900G>A1160192443LUAD
GAIntronicSNV.c.436+11240C>T1160236681CM
GAIntronicSNV.c.436+11587C>T1160236334CM
GAMissensep.P310Sc.928C>T1160209744LUAD
GAMissensep.P53Sc.157C>T1160250033CM
GAMissensep.R271Cc.811C>T1160209861UCEC
GAMissensep.R315Wc.943C>T1160209729MM
GAMissensep.R315Wc.943C>T1160209729UCEC
GANonsensep.R248*c.742C>T1160209930CM
GCMissensep.S449Cc.1346C>G1160207000LUSC
GCNonsensep.S253*c.758C>G1160209914LUAD
GGAAMissensep.R279Cc.834_835delinsTT1160209837CM
GTMissensep.P304Hc.911C>A1160209761UCEC
GTMissensep.Q708Kc.2122C>A1160188131HNSC
TAMissensep.K680Mc.2039A>T1160188214STAD
TAMissensep.R331Sc.993A>T1160209679SCLC
TAMissensep.Y241Fc.722A>T1160209950LUAD
TCCTCTTCCTCT-InFrameDeletionp.E263_E266delEEEEc.765_776delAGAGGAAGAGGA1160209896UCEC
TCMissensep.K8Ec.22A>G1160251960BRCA
TGMissensep.D251Ac.752A>C1160209920LUAD
-TIntronicInsertion.c.436+11541dupA1160236380ESCA