PPP2R2D
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BRCA10133748053133748053+IGRSNPAATTCGA-AN-A0XU-01A-11D-A10G-09TCGA-AN-A0XU-10A-01D-A10G-09g.chr10:133748053A>T
CESC10133757483133757483+5'UTRSNPGGCTCGA-EK-A2PM-01A-11D-A18J-09TCGA-EK-A2PM-10A-01D-A18J-09g.chr10:133757483G>C
CESC10133757608133757608+3'UTRSNPGGTTCGA-C5-A1ML-01A-11D-A14W-08TCGA-C5-A1ML-10A-01D-A14W-08g.chr10:133757608G>T
CESC10133769261133769261+3'UTRSNPGGATCGA-C5-A1BE-01B-11D-A13W-08TCGA-C5-A1BE-10A-01D-A13W-08g.chr10:133769261G>A
COAD10133748002133748004+IGRDELTCTTCT-TCGA-AA-3950-01A-02W-0995-10TCGA-AA-3950-10A-01W-0995-10g.chr10:133748002_133748004delTCT
COAD10133757521133757521+5'UTRSNPGGATCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:133757521G>A
COAD10133761123133761123+SilentSNPCCATCGA-AA-3966-01A-01W-1073-09TCGA-AA-3966-10A-01W-1073-09g.chr10:133761123C>Ac.229C>Ac.(229-231)Cgg>Aggp.R77R
COAD10133761220133761220+Missense_MutationSNPGGATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr10:133761220G>Ac.322G>Ac.(322-324)Gca>Acap.A108T
COAD10133769200133769200+3'UTRSNPCCTTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10g.chr10:133769200C>T
COAD10133769412133769412+3'UTRSNPTTCTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:133769412T>C
COADREAD10133748002133748004+IGRDELTCTTCT-TCGA-AA-3950-01A-02W-0995-10TCGA-AA-3950-10A-01W-0995-10g.chr10:133748002_133748004delTCT
COADREAD10133757518133757518+5'UTRSNPGGATCGA-AG-A02N-01A-11W-A096-10TCGA-AG-A02N-11A-11W-A096-10g.chr10:133757518G>A
COADREAD10133757521133757521+5'UTRSNPGGATCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:133757521G>A
COADREAD10133761123133761123+SilentSNPCCATCGA-AA-3966-01A-01W-1073-09TCGA-AA-3966-10A-01W-1073-09g.chr10:133761123C>Ac.229C>Ac.(229-231)Cgg>Aggp.R77R
COADREAD10133761220133761220+Missense_MutationSNPGGATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr10:133761220G>Ac.322G>Ac.(322-324)Gca>Acap.A108T
COADREAD10133769200133769200+3'UTRSNPCCTTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10g.chr10:133769200C>T
COADREAD10133769412133769412+3'UTRSNPTTCTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr10:133769412T>C
ESCA10133761153133761153+Missense_MutationSNPGGTTCGA-2H-A9GQ-01A-11D-A37C-09TCGA-2H-A9GQ-11A-11D-A37F-09g.chr10:133761153G>Tc.257G>Tc.(256-258)gGt>gTtp.G86V
ESCA10133761171133761171+Missense_MutationSNPAAGTCGA-2H-A9GH-01A-11D-A37C-09TCGA-2H-A9GH-11A-11D-A37F-09g.chr10:133761171A>Gc.275A>Gc.(274-276)cAa>cGap.Q92R
ESCA10133769418133769418+3'UTRSNPCCTTCGA-2H-A9GH-01A-11D-A37C-09TCGA-2H-A9GH-11A-11D-A37F-09g.chr10:133769418C>T
GBMLGG10133758825133758825+Start_Codon_DelDELAA-TCGA-F6-A8O4-01A-11D-A36O-08TCGA-F6-A8O4-10A-01D-A367-08g.chr10:133758825delA
GBMLGG10133761112133761112+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:133761112G>Ac.218G>Ac.(217-219)aGt>aAtp.S73N
HNSC10133758916133758916+Missense_MutationSNPGGATCGA-CV-7432-01A-11D-2129-08TCGA-CV-7432-10A-01D-2129-08g.chr10:133758916G>Ac.92G>Ac.(91-93)cGc>cAcp.R31H
HNSC10133761152133761152+Missense_MutationSNPGGATCGA-BB-8601-01A-11D-2394-08TCGA-BB-8601-10A-01D-2394-08g.chr10:133761152G>Ac.256G>Ac.(256-258)Ggt>Agtp.G86S
HNSC10133769195133769195+SilentSNPAATTCGA-CN-A6V3-01A-12D-A34J-08TCGA-CN-A6V3-10A-01D-A34M-08g.chr10:133769195A>Tc.405A>Tc.(403-405)tcA>tcTp.S135S
KIPAN10133748061133748061+IGRSNPTTGTCGA-CJ-5678-01A-11D-1534-10TCGA-CJ-5678-11A-01D-1534-10g.chr10:133748061T>G
KIRC10133748061133748061+IGRSNPTTGTCGA-CJ-5678-01A-11D-1534-10TCGA-CJ-5678-11A-01D-1534-10g.chr10:133748061T>G
LGG10133758825133758825+Start_Codon_DelDELAA-TCGA-F6-A8O4-01A-11D-A36O-08TCGA-F6-A8O4-10A-01D-A367-08g.chr10:133758825delA
LGG10133761112133761112+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr10:133761112G>Ac.218G>Ac.(217-219)aGt>aAtp.S73N
LUAD10133758916133758916+Missense_MutationSNPGGATCGA-50-5931-01A-11D-1753-08TCGA-50-5931-11A-01D-1753-08g.chr10:133758916G>Ac.92G>Ac.(91-93)cGc>cAcp.R31H
LUAD10133758920133758920+SilentSNPGGATCGA-73-4659-01A-01D-1265-08TCGA-73-4659-11A-01D-1265-08g.chr10:133758920G>Ac.96G>Ac.(94-96)ctG>ctAp.L32L
LUSC10133769242133769242+3'UTRSNPGGTTCGA-66-2787-01A-01D-0983-08TCGA-66-2787-11A-01D-0983-08g.chr10:133769242G>T
LUSC10133769400133769400+3'UTRSNPCCTTCGA-18-3409-01A-01D-0983-08TCGA-18-3409-11A-01D-0983-08g.chr10:133769400C>T
PRAD10133769188133769188+Splice_SiteSNPCCTTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr10:133769188C>Tc.398C>Tc.(397-399)gCg>gTgp.A133V
READ10133757518133757518+5'UTRSNPGGATCGA-AG-A02N-01A-11W-A096-10TCGA-AG-A02N-11A-11W-A096-10g.chr10:133757518G>A
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
AML-US10133761123133761123single base substitutionCT3_prime_UTR_variant
AML-US10133761123133761123single base substitutionCTdownstream_gene_variant
AML-US10133761123133761123single base substitutionCTexon_variant
AML-US10133761123133761123single base substitutionCTmissense_variantR273W817C>T
AML-US10133761123133761123single base substitutionCTmissense_variantR77W229C>T
BLCA-US10133757494133757494single base substitutionAG3_prime_UTR_variant
BLCA-US10133757494133757494single base substitutionAG5_prime_UTR_variant
BLCA-US10133757494133757494single base substitutionAGexon_variant
BLCA-US10133757494133757494single base substitutionAGintron_variant
BLCA-US10133757494133757494single base substitutionAGmissense_variantD136G407A>G
BLCA-US10133769275133769275single base substitutionGC3_prime_UTR_variant
BLCA-US10133769275133769275single base substitutionGCexon_variant
BLCA-US10133769275133769275single base substitutionGCmissense_variantE359D1077G>C
BOCA-FR10133750721133750721single base substitutionGAintron_variant
BOCA-FR10133750721133750721single base substitutionGAupstream_gene_variant
BOCA-FR10133756643133756643single base substitutionCTintron_variant
BRCA-EU10133743018133743018single base substitutionCGupstream_gene_variant
BRCA-EU10133743059133743059single base substitutionCGupstream_gene_variant
BRCA-EU10133744393133744393single base substitutionTCupstream_gene_variant
BRCA-EU10133746050133746050single base substitutionAGupstream_gene_variant
BRCA-EU10133750157133750157single base substitutionAGintron_variant
BRCA-EU10133750157133750157single base substitutionAGupstream_gene_variant
BRCA-EU10133750821133750821single base substitutionACintron_variant
BRCA-EU10133750821133750821single base substitutionACupstream_gene_variant
BRCA-EU10133756556133756556deletion of <=200bpA-intron_variant
BRCA-EU10133756804133756804single base substitutionCTintron_variant
BRCA-EU10133756966133756966single base substitutionATintron_variant
BRCA-EU10133757426133757426single base substitutionGAintron_variant
BRCA-EU10133757564133757564single base substitutionAG3_prime_UTR_variant
BRCA-EU10133757564133757564single base substitutionAG5_prime_UTR_variant
BRCA-EU10133757564133757564single base substitutionAGdownstream_gene_variant
BRCA-EU10133757564133757564single base substitutionAGexon_variant
BRCA-EU10133757564133757564single base substitutionAGintron_variant
BRCA-EU10133757564133757564single base substitutionAGsynonymous_variantS159S477A>G
BRCA-EU10133758552133758552single base substitutionGAdownstream_gene_variant
BRCA-EU10133758552133758552single base substitutionGAintron_variant
BRCA-EU10133764456133764456single base substitutionGCintron_variant
BRCA-EU10133765122133765122single base substitutionCTintron_variant
BRCA-EU10133765313133765313single base substitutionGAintron_variant
BRCA-EU10133765324133765324insertion of <=200bp-Aintron_variant
BRCA-EU10133765334133765334deletion of <=200bpA-intron_variant
BRCA-EU10133768586133768586single base substitutionGCintron_variant
BRCA-EU10133769648133769648single base substitutionCT3_prime_UTR_variant
BRCA-EU10133769648133769648single base substitutionCTdownstream_gene_variant
BRCA-EU10133769648133769648single base substitutionCTexon_variant
BRCA-EU10133769845133769845single base substitutionTA3_prime_UTR_variant
BRCA-EU10133769845133769845single base substitutionTAdownstream_gene_variant
BRCA-EU10133771845133771845single base substitutionGA3_prime_UTR_variant
BRCA-EU10133771845133771845single base substitutionGAdownstream_gene_variant
BRCA-EU10133771912133771912single base substitutionGC3_prime_UTR_variant
BRCA-EU10133771912133771912single base substitutionGCdownstream_gene_variant
BRCA-EU10133772304133772304single base substitutionCG3_prime_UTR_variant
BRCA-EU10133772304133772304single base substitutionCGdownstream_gene_variant
BRCA-EU10133773971133773971single base substitutionTGdownstream_gene_variant
BRCA-EU10133774632133774632single base substitutionCTdownstream_gene_variant
BRCA-EU10133774773133774773single base substitutionGAdownstream_gene_variant
BRCA-EU10133775694133775694single base substitutionGAdownstream_gene_variant
BRCA-EU10133776406133776406single base substitutionCTdownstream_gene_variant
BRCA-EU10133776993133776993single base substitutionCGdownstream_gene_variant
BRCA-EU10133777138133777138single base substitutionGAdownstream_gene_variant
BRCA-EU10133778037133778037single base substitutionTAdownstream_gene_variant
BRCA-FR10133743135133743135single base substitutionGAupstream_gene_variant
BRCA-FR10133756804133756804single base substitutionCTintron_variant
BRCA-FR10133764456133764456single base substitutionGCintron_variant
BRCA-UK10133774088133774088single base substitutionGCdownstream_gene_variant
BRCA-US10133748053133748053single base substitutionATexon_variant
BRCA-US10133748053133748053single base substitutionATmissense_variantE33D99A>T
BTCA-JP10133754280133754280single base substitutionCTexon_variant
BTCA-JP10133754280133754280single base substitutionCTintron_variant
BTCA-JP10133769568133769568single base substitutionGA3_prime_UTR_variant
BTCA-JP10133769568133769568single base substitutionGAdownstream_gene_variant
BTCA-JP10133769568133769568single base substitutionGAexon_variant
CESC-US10133757483133757483single base substitutionGC3_prime_UTR_variant
CESC-US10133757483133757483single base substitutionGC5_prime_UTR_variant
CESC-US10133757483133757483single base substitutionGCexon_variant
CESC-US10133757483133757483single base substitutionGCintron_variant
CESC-US10133757483133757483single base substitutionGCmissense_variantL132F396G>C
CESC-US10133757608133757608single base substitutionGT3_prime_UTR_variant
CESC-US10133757608133757608single base substitutionGT5_prime_UTR_variant
CESC-US10133757608133757608single base substitutionGTdownstream_gene_variant
CESC-US10133757608133757608single base substitutionGTexon_variant
CESC-US10133757608133757608single base substitutionGTmissense_variantR174I521G>T
CESC-US10133769261133769261single base substitutionGA3_prime_UTR_variant
CESC-US10133769261133769261single base substitutionGAexon_variant
CESC-US10133769261133769261single base substitutionGAmissense_variantE355K1063G>A
CLLE-ES10133764867133764867single base substitutionCGintron_variant
COCA-CN10133745371133745371single base substitutionCTupstream_gene_variant
COCA-CN10133746173133746173single base substitutionCAupstream_gene_variant
COCA-CN10133748127133748127single base substitutionGTintron_variant
COCA-CN10133752661133752661single base substitutionCAintron_variant
COCA-CN10133752661133752661single base substitutionCAupstream_gene_variant
COCA-CN10133753745133753745single base substitutionTCintron_variant
COCA-CN10133753745133753745single base substitutionTCupstream_gene_variant
COCA-CN10133757398133757398single base substitutionTCintron_variant
COCA-CN10133767239133767239single base substitutionTGintron_variant
COCA-CN10133769290133769290single base substitutionCT3_prime_UTR_variant
COCA-CN10133769290133769290single base substitutionCTdownstream_gene_variant
COCA-CN10133769290133769290single base substitutionCTexon_variant
COCA-CN10133769290133769290single base substitutionCTsynonymous_variantR364R1092C>T
COCA-CN10133769614133769614single base substitutionTC3_prime_UTR_variant
COCA-CN10133769614133769614single base substitutionTCdownstream_gene_variant
COCA-CN10133769614133769614single base substitutionTCexon_variant
COCA-CN10133772258133772258single base substitutionGA3_prime_UTR_variant
COCA-CN10133772258133772258single base substitutionGAdownstream_gene_variant
COCA-CN10133772323133772323single base substitutionCT3_prime_UTR_variant
COCA-CN10133772323133772323single base substitutionCTdownstream_gene_variant
COCA-CN10133772899133772899single base substitutionAC3_prime_UTR_variant
COCA-CN10133772899133772899single base substitutionACdownstream_gene_variant
COCA-CN10133777410133777410single base substitutionCGdownstream_gene_variant
EOPC-DE10133751616133751616single base substitutionTCintron_variant
EOPC-DE10133751616133751616single base substitutionTCupstream_gene_variant
EOPC-DE10133772171133772171single base substitutionAG3_prime_UTR_variant
EOPC-DE10133772171133772171single base substitutionAGdownstream_gene_variant
EOPC-DE10133772191133772191single base substitutionGA3_prime_UTR_variant
EOPC-DE10133772191133772191single base substitutionGAdownstream_gene_variant
EOPC-DE10133772899133772899single base substitutionAC3_prime_UTR_variant
EOPC-DE10133772899133772899single base substitutionACdownstream_gene_variant
EOPC-DE10133772989133772989single base substitutionTC3_prime_UTR_variant
EOPC-DE10133772989133772989single base substitutionTCdownstream_gene_variant
ESAD-UK10133743211133743211single base substitutionCGupstream_gene_variant
ESAD-UK10133744165133744165single base substitutionCTupstream_gene_variant
ESAD-UK10133748630133748630single base substitutionGTintron_variant
ESAD-UK10133748630133748630single base substitutionGTupstream_gene_variant
ESAD-UK10133750827133750827single base substitutionCTintron_variant
ESAD-UK10133750827133750827single base substitutionCTupstream_gene_variant
ESAD-UK10133751476133751476single base substitutionGAintron_variant
ESAD-UK10133751476133751476single base substitutionGAupstream_gene_variant
ESAD-UK10133754848133754848single base substitutionGAintron_variant
ESAD-UK10133756714133756714single base substitutionGAintron_variant
ESAD-UK10133757375133757375single base substitutionGTintron_variant
ESAD-UK10133764484133764484single base substitutionGAintron_variant
ESAD-UK10133771218133771218single base substitutionGT3_prime_UTR_variant
ESAD-UK10133771218133771218single base substitutionGTdownstream_gene_variant
ESAD-UK10133771989133771989single base substitutionGT3_prime_UTR_variant
ESAD-UK10133771989133771989single base substitutionGTdownstream_gene_variant
ESAD-UK10133775814133775814single base substitutionGTdownstream_gene_variant
ESAD-UK10133776844133776844single base substitutionATdownstream_gene_variant
KIRC-US10133748061133748061single base substitutionTGsplice_donor_variant
LAML-KR10133753407133753407single base substitutionATexon_variant
LAML-KR10133753407133753407single base substitutionATintron_variant
LAML-KR10133753407133753407single base substitutionATupstream_gene_variant
LAML-KR10133766261133766261single base substitutionGAintron_variant
LAML-KR10133766958133766958single base substitutionGTintron_variant
LAML-KR10133766987133766987single base substitutionTCintron_variant
LAML-KR10133771029133771029single base substitutionAG3_prime_UTR_variant
LAML-KR10133771029133771029single base substitutionAGdownstream_gene_variant
LAML-KR10133771379133771379single base substitutionTC3_prime_UTR_variant
LAML-KR10133771379133771379single base substitutionTCdownstream_gene_variant
LAML-KR10133771453133771453single base substitutionTC3_prime_UTR_variant
LAML-KR10133771453133771453single base substitutionTCdownstream_gene_variant
LAML-KR10133771975133771975single base substitutionCA3_prime_UTR_variant
LAML-KR10133771975133771975single base substitutionCAdownstream_gene_variant
LAML-KR10133772043133772043single base substitutionAG3_prime_UTR_variant
LAML-KR10133772043133772043single base substitutionAGdownstream_gene_variant
LAML-KR10133772391133772391single base substitutionTA3_prime_UTR_variant
LAML-KR10133772391133772391single base substitutionTAdownstream_gene_variant
LAML-KR10133772397133772397single base substitutionCT3_prime_UTR_variant
LAML-KR10133772397133772397single base substitutionCTdownstream_gene_variant
LAML-KR10133772521133772521single base substitutionCG3_prime_UTR_variant
LAML-KR10133772521133772521single base substitutionCGdownstream_gene_variant
LAML-KR10133772603133772603single base substitutionAC3_prime_UTR_variant
LAML-KR10133772603133772603single base substitutionACdownstream_gene_variant
LAML-KR10133772746133772746single base substitutionGA3_prime_UTR_variant
LAML-KR10133772746133772746single base substitutionGAdownstream_gene_variant
LGG-US10133748026133748026single base substitutionCTexon_variant
LGG-US10133748026133748026single base substitutionCTsynonymous_variantG24G72C>T
LGG-US10133757525133757525single base substitutionTG3_prime_UTR_variant
LGG-US10133757525133757525single base substitutionTG5_prime_UTR_premature_start_codon_gain_variant
LGG-US10133757525133757525single base substitutionTGdownstream_gene_variant
LGG-US10133757525133757525single base substitutionTGexon_variant
LGG-US10133757525133757525single base substitutionTGintron_variant
LGG-US10133757525133757525single base substitutionTGmissense_variantI146M438T>G
LICA-CN10133757620133757620single base substitutionGT3_prime_UTR_variant
LICA-CN10133757620133757620single base substitutionGT5_prime_UTR_premature_start_codon_gain_variant
LICA-CN10133757620133757620single base substitutionGTdownstream_gene_variant
LICA-CN10133757620133757620single base substitutionGTexon_variant
LICA-CN10133757620133757620single base substitutionGTmissense_variantW178L533G>T
LICA-FR10133753240133753240single base substitutionGAintron_variant
LICA-FR10133753240133753240single base substitutionGAupstream_gene_variant
LICA-FR10133772521133772521single base substitutionCG3_prime_UTR_variant
LICA-FR10133772521133772521single base substitutionCGdownstream_gene_variant
LICA-FR10133772603133772603single base substitutionAC3_prime_UTR_variant
LICA-FR10133772603133772603single base substitutionACdownstream_gene_variant
LICA-FR10133773071133773071single base substitutionCA3_prime_UTR_variant
LICA-FR10133773071133773071single base substitutionCAdownstream_gene_variant
LICA-FR10133777390133777395deletion of <=200bpCACCTG-downstream_gene_variant
LINC-JP10133752616133752616single base substitutionGAintron_variant
LINC-JP10133752616133752616single base substitutionGAupstream_gene_variant
LINC-JP10133752624133752624single base substitutionCAintron_variant
LINC-JP10133752624133752624single base substitutionCAupstream_gene_variant
LINC-JP10133753547133753547single base substitutionCT3_prime_UTR_variant
LINC-JP10133753547133753547single base substitutionCT5_prime_UTR_variant
LINC-JP10133753547133753547single base substitutionCTexon_variant
LINC-JP10133753547133753547single base substitutionCTmissense_variantP40S118C>T
LINC-JP10133753547133753547single base substitutionCTupstream_gene_variant
LINC-JP10133753727133753727single base substitutionTGintron_variant
LINC-JP10133753727133753727single base substitutionTGupstream_gene_variant
LINC-JP10133754754133754754single base substitutionACintron_variant
LINC-JP10133757407133757407single base substitutionAGintron_variant
LINC-JP10133757521133757521single base substitutionGA3_prime_UTR_variant
LINC-JP10133757521133757521single base substitutionGA5_prime_UTR_variant
LINC-JP10133757521133757521single base substitutionGAdownstream_gene_variant
LINC-JP10133757521133757521single base substitutionGAexon_variant
LINC-JP10133757521133757521single base substitutionGAintron_variant
LINC-JP10133757521133757521single base substitutionGAmissense_variantR145Q434G>A
LINC-JP10133757858133757858single base substitutionAGdownstream_gene_variant
LINC-JP10133757858133757858single base substitutionAGintron_variant
LINC-JP10133762248133762249deletion of <=200bpCA-downstream_gene_variant
LINC-JP10133762248133762249deletion of <=200bpCA-intron_variant
LINC-JP10133766362133766362deletion of <=200bpG-intron_variant
LIRI-JP10133743625133743625single base substitutionATupstream_gene_variant
LIRI-JP10133744224133744224single base substitutionGTupstream_gene_variant
LIRI-JP10133744269133744269single base substitutionGTupstream_gene_variant
LIRI-JP10133744637133744637single base substitutionAGupstream_gene_variant
LIRI-JP10133745055133745055single base substitutionTGupstream_gene_variant
LIRI-JP10133747158133747158single base substitutionCGupstream_gene_variant
LIRI-JP10133747459133747459single base substitutionAGupstream_gene_variant
LIRI-JP10133756877133756877single base substitutionAGintron_variant
LIRI-JP10133759601133759601single base substitutionCTdownstream_gene_variant
LIRI-JP10133759601133759601single base substitutionCTintron_variant
LIRI-JP10133759709133759709single base substitutionTCdownstream_gene_variant
LIRI-JP10133759709133759709single base substitutionTCintron_variant
LIRI-JP10133760753133760753single base substitutionCTdownstream_gene_variant
LIRI-JP10133760753133760753single base substitutionCTintron_variant
LIRI-JP10133761395133761395single base substitutionGAdownstream_gene_variant
LIRI-JP10133761395133761395single base substitutionGAintron_variant
LIRI-JP10133762344133762344single base substitutionAGdownstream_gene_variant
LIRI-JP10133762344133762344single base substitutionAGintron_variant
LIRI-JP10133764234133764234deletion of <=200bpC-downstream_gene_variant
LIRI-JP10133764234133764234deletion of <=200bpC-intron_variant
LIRI-JP10133764525133764525single base substitutionTAintron_variant
LIRI-JP10133768070133768070single base substitutionAGintron_variant
LIRI-JP10133768108133768108single base substitutionAGintron_variant
LIRI-JP10133769690133769690single base substitutionGA3_prime_UTR_variant
LIRI-JP10133769690133769690single base substitutionGAdownstream_gene_variant
LIRI-JP10133769690133769690single base substitutionGAexon_variant
LIRI-JP10133776734133776734single base substitutionACdownstream_gene_variant
LUSC-KR10133743952133743952single base substitutionCTupstream_gene_variant
LUSC-KR10133754623133754623single base substitutionGAintron_variant
LUSC-KR10133760101133760101single base substitutionAGdownstream_gene_variant
LUSC-KR10133760101133760101single base substitutionAGintron_variant
LUSC-KR10133764055133764055single base substitutionGAdownstream_gene_variant
LUSC-KR10133764055133764055single base substitutionGAintron_variant
LUSC-KR10133766506133766506single base substitutionAGintron_variant
LUSC-KR10133766930133766930single base substitutionGTintron_variant
LUSC-KR10133767097133767097single base substitutionCTintron_variant
LUSC-KR10133769568133769568single base substitutionGA3_prime_UTR_variant
LUSC-KR10133769568133769568single base substitutionGAdownstream_gene_variant
LUSC-KR10133769568133769568single base substitutionGAexon_variant
LUSC-KR10133771029133771029single base substitutionAG3_prime_UTR_variant
LUSC-KR10133771029133771029single base substitutionAGdownstream_gene_variant
LUSC-KR10133771461133771461single base substitutionAG3_prime_UTR_variant
LUSC-KR10133771461133771461single base substitutionAGdownstream_gene_variant
LUSC-KR10133771993133771993single base substitutionAG3_prime_UTR_variant
LUSC-KR10133771993133771993single base substitutionAGdownstream_gene_variant
LUSC-KR10133772174133772174single base substitutionAG3_prime_UTR_variant
LUSC-KR10133772174133772174single base substitutionAGdownstream_gene_variant
LUSC-KR10133772391133772391single base substitutionTA3_prime_UTR_variant
LUSC-KR10133772391133772391single base substitutionTAdownstream_gene_variant
LUSC-KR10133772849133772849single base substitutionCG3_prime_UTR_variant
LUSC-KR10133772849133772849single base substitutionCGdownstream_gene_variant
LUSC-KR10133772952133772952single base substitutionCT3_prime_UTR_variant
LUSC-KR10133772952133772952single base substitutionCTdownstream_gene_variant
LUSC-US10133769242133769242single base substitutionGT3_prime_UTR_variant
LUSC-US10133769242133769242single base substitutionGTexon_variant
LUSC-US10133769242133769242single base substitutionGTsynonymous_variantT348T1044G>T
LUSC-US10133769400133769400single base substitutionCT3_prime_UTR_variant
LUSC-US10133769400133769400single base substitutionCTdownstream_gene_variant
LUSC-US10133769400133769400single base substitutionCTexon_variant
LUSC-US10133769400133769400single base substitutionCTmissense_variantP401L1202C>T
MALY-DE10133749130133749130single base substitutionTAintron_variant
MALY-DE10133749130133749130single base substitutionTAupstream_gene_variant
MALY-DE10133750536133750536single base substitutionCTintron_variant
MALY-DE10133750536133750536single base substitutionCTupstream_gene_variant
MALY-DE10133750580133750580single base substitutionATintron_variant
MALY-DE10133750580133750580single base substitutionATupstream_gene_variant
MALY-DE10133750913133750913insertion of <=200bp-Aintron_variant
MALY-DE10133750913133750913insertion of <=200bp-Aupstream_gene_variant
MALY-DE10133772302133772302single base substitutionGA3_prime_UTR_variant
MALY-DE10133772302133772302single base substitutionGAdownstream_gene_variant
MALY-DE10133773175133773175single base substitutionCG3_prime_UTR_variant
MALY-DE10133773175133773175single base substitutionCGdownstream_gene_variant
MALY-DE10133776909133776909single base substitutionGAdownstream_gene_variant
MALY-DE10133777437133777437single base substitutionTGdownstream_gene_variant
MELA-AU10133743165133743165single base substitutionCTupstream_gene_variant
MELA-AU10133743261133743261single base substitutionCTupstream_gene_variant
MELA-AU10133743448133743448single base substitutionCTupstream_gene_variant
MELA-AU10133743603133743603single base substitutionCTupstream_gene_variant
MELA-AU10133743816133743816single base substitutionCTupstream_gene_variant
MELA-AU10133743912133743912single base substitutionCTupstream_gene_variant
MELA-AU10133744733133744733single base substitutionCTupstream_gene_variant
MELA-AU10133745093133745093single base substitutionCTupstream_gene_variant
MELA-AU10133745409133745409single base substitutionCTupstream_gene_variant
MELA-AU10133746823133746823single base substitutionCAupstream_gene_variant
MELA-AU10133747251133747251single base substitutionCTupstream_gene_variant
MELA-AU10133747290133747290single base substitutionCTupstream_gene_variant
MELA-AU10133748286133748286single base substitutionCTintron_variant
MELA-AU10133748286133748286single base substitutionCTupstream_gene_variant
MELA-AU10133748287133748287single base substitutionCTintron_variant
MELA-AU10133748287133748287single base substitutionCTupstream_gene_variant
MELA-AU10133748378133748378single base substitutionCTintron_variant
MELA-AU10133748378133748378single base substitutionCTupstream_gene_variant
MELA-AU10133748389133748389single base substitutionCTintron_variant
MELA-AU10133748389133748389single base substitutionCTupstream_gene_variant
MELA-AU10133748538133748538single base substitutionCTintron_variant
MELA-AU10133748538133748538single base substitutionCTupstream_gene_variant
MELA-AU10133748954133748954single base substitutionCTintron_variant
MELA-AU10133748954133748954single base substitutionCTupstream_gene_variant
MELA-AU10133749025133749026multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU10133749025133749026multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU10133749782133749782single base substitutionCTintron_variant
MELA-AU10133749782133749782single base substitutionCTupstream_gene_variant
MELA-AU10133750103133750103single base substitutionCTintron_variant
MELA-AU10133750103133750103single base substitutionCTupstream_gene_variant
MELA-AU10133750935133750935single base substitutionCTintron_variant
MELA-AU10133750935133750935single base substitutionCTupstream_gene_variant
MELA-AU10133750937133750938multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU10133750937133750938multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU10133751312133751312single base substitutionCTintron_variant
MELA-AU10133751312133751312single base substitutionCTupstream_gene_variant
MELA-AU10133751973133751973single base substitutionCTintron_variant
MELA-AU10133751973133751973single base substitutionCTupstream_gene_variant
MELA-AU10133752047133752047single base substitutionCTintron_variant
MELA-AU10133752047133752047single base substitutionCTupstream_gene_variant
MELA-AU10133752205133752205single base substitutionCTintron_variant
MELA-AU10133752205133752205single base substitutionCTupstream_gene_variant
MELA-AU10133753210133753210single base substitutionCTintron_variant
MELA-AU10133753210133753210single base substitutionCTupstream_gene_variant
MELA-AU10133755655133755655single base substitutionCTintron_variant
MELA-AU10133756175133756175single base substitutionCTintron_variant
MELA-AU10133756474133756474single base substitutionCTintron_variant
MELA-AU10133756642133756642single base substitutionCTintron_variant
MELA-AU10133756759133756759single base substitutionCTintron_variant
MELA-AU10133757389133757389single base substitutionCTintron_variant
MELA-AU10133757829133757829single base substitutionCTdownstream_gene_variant
MELA-AU10133757829133757829single base substitutionCTintron_variant
MELA-AU10133758094133758094single base substitutionCTdownstream_gene_variant
MELA-AU10133758094133758094single base substitutionCTintron_variant
MELA-AU10133758574133758574single base substitutionCTdownstream_gene_variant
MELA-AU10133758574133758574single base substitutionCTintron_variant
MELA-AU10133758803133758803single base substitutionCT3_prime_UTR_variant
MELA-AU10133758803133758803single base substitutionCT5_prime_UTR_premature_start_codon_gain_variant
MELA-AU10133758803133758803single base substitutionCTdownstream_gene_variant
MELA-AU10133758803133758803single base substitutionCTexon_variant
MELA-AU10133758803133758803single base substitutionCTsynonymous_variantI189I567C>T
MELA-AU10133760040133760040single base substitutionGTdownstream_gene_variant
MELA-AU10133760040133760040single base substitutionGTintron_variant
MELA-AU10133760714133760714single base substitutionCTdownstream_gene_variant
MELA-AU10133760714133760714single base substitutionCTintron_variant
MELA-AU10133761031133761031single base substitutionCTdownstream_gene_variant
MELA-AU10133761031133761031single base substitutionCTsplice_region_variant
MELA-AU10133761054133761054single base substitutionCT3_prime_UTR_variant
MELA-AU10133761054133761054single base substitutionCTdownstream_gene_variant
MELA-AU10133761054133761054single base substitutionCTexon_variant
MELA-AU10133761054133761054single base substitutionCTmissense_variantP250S748C>T
MELA-AU10133761054133761054single base substitutionCTmissense_variantP54S160C>T
MELA-AU10133761071133761071single base substitutionCT3_prime_UTR_variant
MELA-AU10133761071133761071single base substitutionCTdownstream_gene_variant
MELA-AU10133761071133761071single base substitutionCTexon_variant
MELA-AU10133761071133761071single base substitutionCTsynonymous_variantF255F765C>T
MELA-AU10133761071133761071single base substitutionCTsynonymous_variantF59F177C>T
MELA-AU10133761417133761417single base substitutionCTdownstream_gene_variant
MELA-AU10133761417133761417single base substitutionCTintron_variant
MELA-AU10133762143133762143single base substitutionCTdownstream_gene_variant
MELA-AU10133762143133762143single base substitutionCTintron_variant
MELA-AU10133762160133762161multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU10133762160133762161multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU10133762889133762889single base substitutionGAdownstream_gene_variant
MELA-AU10133762889133762889single base substitutionGAintron_variant
MELA-AU10133762907133762907single base substitutionCTdownstream_gene_variant
MELA-AU10133762907133762907single base substitutionCTintron_variant
MELA-AU10133763106133763106single base substitutionAGdownstream_gene_variant
MELA-AU10133763106133763106single base substitutionAGintron_variant
MELA-AU10133763915133763915single base substitutionAGdownstream_gene_variant
MELA-AU10133763915133763915single base substitutionAGintron_variant
MELA-AU10133764049133764049single base substitutionCTdownstream_gene_variant
MELA-AU10133764049133764049single base substitutionCTintron_variant
MELA-AU10133765153133765153single base substitutionCTintron_variant
MELA-AU10133767641133767642multiple base substitution (>=2bp and <=200bp)CCTAintron_variant
MELA-AU10133769061133769061single base substitutionTCintron_variant
MELA-AU10133769699133769699single base substitutionGA3_prime_UTR_variant
MELA-AU10133769699133769699single base substitutionGAdownstream_gene_variant
MELA-AU10133769699133769699single base substitutionGAexon_variant
MELA-AU10133769908133769908single base substitutionCA3_prime_UTR_variant
MELA-AU10133769908133769908single base substitutionCAdownstream_gene_variant
MELA-AU10133770855133770855single base substitutionCT3_prime_UTR_variant
MELA-AU10133770855133770855single base substitutionCTdownstream_gene_variant
MELA-AU10133771141133771141single base substitutionGA3_prime_UTR_variant
MELA-AU10133771141133771141single base substitutionGAdownstream_gene_variant
MELA-AU10133771316133771316single base substitutionGA3_prime_UTR_variant
MELA-AU10133771316133771316single base substitutionGAdownstream_gene_variant
MELA-AU10133771528133771528single base substitutionCT3_prime_UTR_variant
MELA-AU10133771528133771528single base substitutionCTdownstream_gene_variant
MELA-AU10133771650133771650single base substitutionGA3_prime_UTR_variant
MELA-AU10133771650133771650single base substitutionGAdownstream_gene_variant
MELA-AU10133772305133772305single base substitutionCT3_prime_UTR_variant
MELA-AU10133772305133772305single base substitutionCTdownstream_gene_variant
MELA-AU10133773009133773009single base substitutionCT3_prime_UTR_variant
MELA-AU10133773009133773009single base substitutionCTdownstream_gene_variant
MELA-AU10133773758133773758single base substitutionCTdownstream_gene_variant
MELA-AU10133774022133774022single base substitutionCAdownstream_gene_variant
MELA-AU10133774055133774055single base substitutionCTdownstream_gene_variant
MELA-AU10133774674133774675multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU10133774800133774800single base substitutionGAdownstream_gene_variant
MELA-AU10133775302133775302single base substitutionCTdownstream_gene_variant
MELA-AU10133776771133776771single base substitutionCTdownstream_gene_variant
MELA-AU10133776975133776975single base substitutionCTdownstream_gene_variant
MELA-AU10133777403133777403single base substitutionCTdownstream_gene_variant
MELA-AU10133777644133777644single base substitutionGAdownstream_gene_variant
MELA-AU10133777853133777853single base substitutionTCdownstream_gene_variant
ORCA-IN10133753539133753539single base substitutionAG3_prime_UTR_variant
ORCA-IN10133753539133753539single base substitutionAG5_prime_UTR_variant
ORCA-IN10133753539133753539single base substitutionAGexon_variant
ORCA-IN10133753539133753539single base substitutionAGmissense_variantK37R110A>G
ORCA-IN10133753539133753539single base substitutionAGupstream_gene_variant
ORCA-IN10133770063133770063single base substitutionTG3_prime_UTR_variant
ORCA-IN10133770063133770063single base substitutionTGdownstream_gene_variant
ORCA-IN10133774716133774716single base substitutionGAdownstream_gene_variant
OV-AU10133760165133760165single base substitutionTCdownstream_gene_variant
OV-AU10133760165133760165single base substitutionTCintron_variant
OV-AU10133775169133775169single base substitutionGAdownstream_gene_variant
PACA-AU10133746171133746171single base substitutionACupstream_gene_variant
PACA-AU10133757392133757392single base substitutionCGintron_variant
PACA-AU10133758171133758171single base substitutionCTdownstream_gene_variant
PACA-AU10133758171133758171single base substitutionCTintron_variant
PACA-AU10133766497133766497single base substitutionCTintron_variant
PACA-AU10133768285133768285single base substitutionGAintron_variant
PACA-AU10133769959133769959single base substitutionTA3_prime_UTR_variant
PACA-AU10133769959133769959single base substitutionTAdownstream_gene_variant
PACA-AU10133770657133770657single base substitutionGC3_prime_UTR_variant
PACA-AU10133770657133770657single base substitutionGCdownstream_gene_variant
PACA-AU10133776601133776601single base substitutionGAdownstream_gene_variant
PACA-AU10133776882133776882single base substitutionATdownstream_gene_variant
PACA-CA10133743179133743179single base substitutionCAupstream_gene_variant
PACA-CA10133745815133745815single base substitutionGAupstream_gene_variant
PACA-CA10133747023133747023single base substitutionCTupstream_gene_variant
PACA-CA10133749276133749276single base substitutionCTintron_variant
PACA-CA10133749276133749276single base substitutionCTupstream_gene_variant
PACA-CA10133750462133750462single base substitutionGAintron_variant
PACA-CA10133750462133750462single base substitutionGAupstream_gene_variant
PACA-CA10133751814133751814single base substitutionTCintron_variant
PACA-CA10133751814133751814single base substitutionTCupstream_gene_variant
PACA-CA10133755301133755301single base substitutionTCintron_variant
PACA-CA10133761233133761236deletion of <=200bpCTCT-3_prime_UTR_variant
PACA-CA10133761233133761236deletion of <=200bpCTCT-downstream_gene_variant
PACA-CA10133761233133761236deletion of <=200bpCTCT-exon_variant
PACA-CA10133761233133761236deletion of <=200bpCTCT-frameshift_variantAL112
PACA-CA10133761233133761236deletion of <=200bpCTCT-frameshift_variantCS309
PACA-CA10133769409133769409single base substitutionAG3_prime_UTR_variant
PACA-CA10133769409133769409single base substitutionAGdownstream_gene_variant
PACA-CA10133769409133769409single base substitutionAGexon_variant
PACA-CA10133769409133769409single base substitutionAGmissense_variantN404S1211A>G
PACA-CA10133769467133769467single base substitutionGT3_prime_UTR_variant
PACA-CA10133769467133769467single base substitutionGTdownstream_gene_variant
PACA-CA10133769467133769467single base substitutionGTexon_variant
PACA-CA10133769467133769467single base substitutionGTstop_lost*423Y1269G>T
PACA-CA10133770230133770230single base substitutionGT3_prime_UTR_variant
PACA-CA10133770230133770230single base substitutionGTdownstream_gene_variant
PACA-CA10133770264133770264single base substitutionCT3_prime_UTR_variant
PACA-CA10133770264133770264single base substitutionCTdownstream_gene_variant
PACA-CA10133770372133770372single base substitutionCG3_prime_UTR_variant
PACA-CA10133770372133770372single base substitutionCGdownstream_gene_variant
PACA-CA10133771993133771993single base substitutionAG3_prime_UTR_variant
PACA-CA10133771993133771993single base substitutionAGdownstream_gene_variant
PACA-CA10133772484133772484single base substitutionGC3_prime_UTR_variant
PACA-CA10133772484133772484single base substitutionGCdownstream_gene_variant
PACA-CA10133772603133772603single base substitutionAC3_prime_UTR_variant
PACA-CA10133772603133772603single base substitutionACdownstream_gene_variant
PACA-CA10133775735133775735single base substitutionGAdownstream_gene_variant
PACA-CA10133777049133777049single base substitutionGAdownstream_gene_variant
PACA-CA10133777190133777190single base substitutionGAdownstream_gene_variant
PACA-CA10133778132133778132single base substitutionAGdownstream_gene_variant
PAEN-AU10133772709133772709single base substitutionGA3_prime_UTR_variant
PAEN-AU10133772709133772709single base substitutionGAdownstream_gene_variant
PBCA-DE10133745826133745826single base substitutionCGupstream_gene_variant
PBCA-DE10133760657133760657single base substitutionCTdownstream_gene_variant
PBCA-DE10133760657133760657single base substitutionCTintron_variant
PBCA-DE10133760988133760988single base substitutionTCdownstream_gene_variant
PBCA-DE10133760988133760988single base substitutionTCintron_variant
PBCA-DE10133766506133766506deletion of <=200bpA-intron_variant
PBCA-DE10133766675133766675single base substitutionGAintron_variant
PBCA-DE10133771567133771567single base substitutionAC3_prime_UTR_variant
PBCA-DE10133771567133771567single base substitutionACdownstream_gene_variant
PBCA-DE10133772492133772492single base substitutionAC3_prime_UTR_variant
PBCA-DE10133772492133772492single base substitutionACdownstream_gene_variant
PRAD-CA10133753170133753170single base substitutionAGintron_variant
PRAD-CA10133753170133753170single base substitutionAGupstream_gene_variant
PRAD-CA10133755854133755854single base substitutionGAintron_variant
PRAD-CA10133772780133772780single base substitutionGC3_prime_UTR_variant
PRAD-CA10133772780133772780single base substitutionGCdownstream_gene_variant
PRAD-CA10133775102133775102single base substitutionGAdownstream_gene_variant
PRAD-UK10133750955133750965deletion of <=200bpTTCCCTGCTCT-intron_variant
PRAD-UK10133750955133750965deletion of <=200bpTTCCCTGCTCT-upstream_gene_variant
PRAD-UK10133751536133751536single base substitutionGAintron_variant
PRAD-UK10133751536133751536single base substitutionGAupstream_gene_variant
PRAD-UK10133760759133760759single base substitutionATdownstream_gene_variant
PRAD-UK10133760759133760759single base substitutionATintron_variant
PRAD-UK10133767208133767240deletion of <=200bpGTGTGGGGGGGTCACTGTCTTAGTGACTTGCTG-intron_variant
PRAD-UK10133771696133771696single base substitutionGA3_prime_UTR_variant
PRAD-UK10133771696133771696single base substitutionGAdownstream_gene_variant
PRAD-UK10133772706133772706single base substitutionCG3_prime_UTR_variant
PRAD-UK10133772706133772706single base substitutionCGdownstream_gene_variant
PRAD-UK10133774324133774325deletion of <=200bpGA-downstream_gene_variant
RECA-EU10133749902133749902single base substitutionGCintron_variant
RECA-EU10133749902133749902single base substitutionGCupstream_gene_variant
RECA-EU10133756867133756867single base substitutionCTintron_variant
RECA-EU10133758653133758653single base substitutionATdownstream_gene_variant
RECA-EU10133758653133758653single base substitutionATintron_variant
RECA-EU10133761546133761546single base substitutionTCdownstream_gene_variant
RECA-EU10133761546133761546single base substitutionTCintron_variant
RECA-EU10133767677133767677single base substitutionAGintron_variant
SKCA-BR10133743339133743339single base substitutionACupstream_gene_variant
SKCA-BR10133748602133748602single base substitutionCTintron_variant
SKCA-BR10133748602133748602single base substitutionCTupstream_gene_variant
SKCA-BR10133754632133754632single base substitutionCTintron_variant
SKCA-BR10133754967133754967single base substitutionCTintron_variant
SKCA-BR10133757458133757458single base substitutionCTintron_variant
SKCA-BR10133759496133759496single base substitutionTGdownstream_gene_variant
SKCA-BR10133759496133759496single base substitutionTGintron_variant
SKCA-BR10133760497133760497single base substitutionTGdownstream_gene_variant
SKCA-BR10133760497133760497single base substitutionTGintron_variant
SKCA-BR10133760774133760774single base substitutionCTdownstream_gene_variant
SKCA-BR10133760774133760774single base substitutionCTintron_variant
SKCA-BR10133762280133762280single base substitutionCTdownstream_gene_variant
SKCA-BR10133762280133762280single base substitutionCTintron_variant
SKCA-BR10133762668133762668single base substitutionCTdownstream_gene_variant
SKCA-BR10133762668133762668single base substitutionCTintron_variant
SKCA-BR10133766826133766861deletion of <=200bpCGGGGGTTCACTGTCTTAGTGACTTCCAGTTGTGCG-intron_variant
SKCA-BR10133767387133767387single base substitutionATintron_variant
SKCA-BR10133767935133767935single base substitutionACintron_variant
SKCA-BR10133771164133771164single base substitutionAC3_prime_UTR_variant
SKCA-BR10133771164133771164single base substitutionACdownstream_gene_variant
SKCA-BR10133771196133771196single base substitutionGA3_prime_UTR_variant
SKCA-BR10133771196133771196single base substitutionGAdownstream_gene_variant
SKCA-BR10133771272133771272single base substitutionGC3_prime_UTR_variant
SKCA-BR10133771272133771272single base substitutionGCdownstream_gene_variant
SKCA-BR10133771585133771585single base substitutionGA3_prime_UTR_variant
SKCA-BR10133771585133771585single base substitutionGAdownstream_gene_variant
SKCA-BR10133771686133771723deletion of <=200bpGGAGGTGTGTGCTGATCCCTCGTGCCCCTGTGGAGATA-3_prime_UTR_variant
SKCA-BR10133771686133771723deletion of <=200bpGGAGGTGTGTGCTGATCCCTCGTGCCCCTGTGGAGATA-downstream_gene_variant
SKCA-BR10133772022133772022single base substitutionGA3_prime_UTR_variant
SKCA-BR10133772022133772022single base substitutionGAdownstream_gene_variant
SKCA-BR10133772079133772079single base substitutionTC3_prime_UTR_variant
SKCA-BR10133772079133772079single base substitutionTCdownstream_gene_variant
SKCA-BR10133772195133772195single base substitutionTC3_prime_UTR_variant
SKCA-BR10133772195133772195single base substitutionTCdownstream_gene_variant
SKCA-BR10133772381133772381single base substitutionAC3_prime_UTR_variant
SKCA-BR10133772381133772381single base substitutionACdownstream_gene_variant
SKCA-BR10133772842133772842single base substitutionGA3_prime_UTR_variant
SKCA-BR10133772842133772842single base substitutionGAdownstream_gene_variant
SKCA-BR10133772899133772899single base substitutionAC3_prime_UTR_variant
SKCA-BR10133772899133772899single base substitutionACdownstream_gene_variant
SKCA-BR10133778170133778170insertion of <=200bp-GTdownstream_gene_variant
SKCM-US10133769225133769225single base substitutionAT3_prime_UTR_variant
SKCM-US10133769225133769225single base substitutionATexon_variant
SKCM-US10133769225133769225single base substitutionATmissense_variantM343L1027A>T
SKCM-US10133769419133769419single base substitutionCT3_prime_UTR_variant
SKCM-US10133769419133769419single base substitutionCTdownstream_gene_variant
SKCM-US10133769419133769419single base substitutionCTexon_variant
SKCM-US10133769419133769419single base substitutionCTsynonymous_variantA407A1221C>T
STAD-US10133753565133753565single base substitutionTC3_prime_UTR_variant
STAD-US10133753565133753565single base substitutionTC5_prime_UTR_variant
STAD-US10133753565133753565single base substitutionTCexon_variant
STAD-US10133753565133753565single base substitutionTCmissense_variantY46H136T>C
STAD-US10133753565133753565single base substitutionTCupstream_gene_variant
STAD-US10133754196133754196single base substitutionCTexon_variant
STAD-US10133754196133754196single base substitutionCTmissense_variantR128W382C>T
STAD-US10133754196133754196single base substitutionCTsplice_region_variant
STAD-US10133757520133757520single base substitutionCT3_prime_UTR_variant
STAD-US10133757520133757520single base substitutionCT5_prime_UTR_variant
STAD-US10133757520133757520single base substitutionCTdownstream_gene_variant
STAD-US10133757520133757520single base substitutionCTexon_variant
STAD-US10133757520133757520single base substitutionCTintron_variant
STAD-US10133757520133757520single base substitutionCTstop_gainedR145*433C>T
STAD-US10133758887133758887single base substitutionCT3_prime_UTR_variant
STAD-US10133758887133758887single base substitutionCTdownstream_gene_variant
STAD-US10133758887133758887single base substitutionCTexon_variant
STAD-US10133758887133758887single base substitutionCTsynonymous_variantF217F651C>T
STAD-US10133758887133758887single base substitutionCTsynonymous_variantF21F63C>T
STAD-US10133761176133761176single base substitutionGA3_prime_UTR_variant
STAD-US10133761176133761176single base substitutionGAdownstream_gene_variant
STAD-US10133761176133761176single base substitutionGAexon_variant
STAD-US10133761176133761176single base substitutionGAmissense_variantM290I870G>A
STAD-US10133761176133761176single base substitutionGAsplice_acceptor_variant
STAD-US10133769241133769241single base substitutionCT3_prime_UTR_variant
STAD-US10133769241133769241single base substitutionCTexon_variant
STAD-US10133769241133769241single base substitutionCTmissense_variantT348M1043C>T
STAD-US10133769302133769302single base substitutionAC3_prime_UTR_variant
STAD-US10133769302133769302single base substitutionACdownstream_gene_variant
STAD-US10133769302133769302single base substitutionACexon_variant
STAD-US10133769302133769302single base substitutionACmissense_variantK368N1104A>C
UCEC-US10133747979133747979single base substitutionGAexon_variant
UCEC-US10133747979133747979single base substitutionGAmissense_variantV9I25G>A
UCEC-US10133748048133748048single base substitutionCTexon_variant
UCEC-US10133748048133748048single base substitutionCTmissense_variantR32C94C>T
UCEC-US10133754154133754154single base substitutionGA3_prime_UTR_variant
UCEC-US10133754154133754154single base substitutionGA5_prime_UTR_variant
UCEC-US10133754154133754154single base substitutionGAexon_variant
UCEC-US10133754154133754154single base substitutionGAmissense_variantE114K340G>A
UCEC-US10133758931133758931single base substitutionGA3_prime_UTR_variant
UCEC-US10133758931133758931single base substitutionGAdownstream_gene_variant
UCEC-US10133758931133758931single base substitutionGAexon_variant
UCEC-US10133758931133758931single base substitutionGAmissense_variantR232H695G>A
UCEC-US10133758931133758931single base substitutionGAmissense_variantR36H107G>A
UCEC-US10133761123133761123single base substitutionCT3_prime_UTR_variant
UCEC-US10133761123133761123single base substitutionCTdownstream_gene_variant
UCEC-US10133761123133761123single base substitutionCTexon_variant
UCEC-US10133761123133761123single base substitutionCTmissense_variantR273W817C>T
UCEC-US10133761123133761123single base substitutionCTmissense_variantR77W229C>T
UCEC-US10133761150133761150single base substitutionTG3_prime_UTR_variant
UCEC-US10133761150133761150single base substitutionTGdownstream_gene_variant
UCEC-US10133761150133761150single base substitutionTGexon_variant
UCEC-US10133761150133761150single base substitutionTGmissense_variantS282A844T>G
UCEC-US10133761150133761150single base substitutionTGmissense_variantV85G254T>G
UCEC-US10133761248133761248single base substitutionCT3_prime_UTR_variant
UCEC-US10133761248133761248single base substitutionCTdownstream_gene_variant
UCEC-US10133761248133761248single base substitutionCTexon_variant
UCEC-US10133761248133761248single base substitutionCTmissense_variantT117M350C>T
UCEC-US10133761248133761248single base substitutionCTsynonymous_variantN314N942C>T
UCEC-US10133761257133761257single base substitutionCA3_prime_UTR_variant
UCEC-US10133761257133761257single base substitutionCAdownstream_gene_variant
UCEC-US10133761257133761257single base substitutionCAexon_variant
UCEC-US10133761257133761257single base substitutionCAmissense_variantS120Y359C>A
UCEC-US10133761257133761257single base substitutionCAsynonymous_variantI317I951C>A
UCEC-US10133761289133761289single base substitutionCT3_prime_UTR_variant
UCEC-US10133761289133761289single base substitutionCTdownstream_gene_variant
UCEC-US10133761289133761289single base substitutionCTexon_variant
UCEC-US10133761289133761289single base substitutionCTmissense_variantR131W391C>T
UCEC-US10133761289133761289single base substitutionCTmissense_variantS328L983C>T
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-CJ-5678-01COSM465445c.105+2T>Gp.?Unknown10:131934557-131934557+
TCGA-HT-7602-01COSM3966958c.438T>Gp.I146MSubstitution - Missense10:131944021-131944021+
HN_62298COSM125545c.416G>Ap.G139ESubstitution - Missense10:131955698-131955698+
EGC15COSM284194c.326G>Ap.R109HSubstitution - Missense10:131947716-131947716+
TCGA-CG-5723-01COSM4012747c.1104A>Cp.K368NSubstitution - Missense10:131955798-131955798+
sysucc-1370TCOSM5469371c.504C>Tp.R168RSubstitution - coding silent10:131955786-131955786+
TCGA-CS-5390-01COSM3966957c.72C>Tp.G24GSubstitution - coding silent10:131934522-131934522+
TCGA-CG-4449-01COSM4012740c.433C>Tp.R145*Substitution - Nonsense10:131944016-131944016+
169COSM3729974c.1122delGp.G376fs*>47Deletion - Frameshift10:131955816-131955816+
S02293COSM5688377c.458G>Ap.R153QSubstitution - Missense10:131955740-131955740+
TARGET-30-PARNNGCOSM1287344c.684G>Cp.L228LSubstitution - coding silent10:131945416-131945416+
EGC15COSM4012745c.1043C>Tp.T348MSubstitution - Missense10:131955737-131955737+
WT030COSM5351945c.150G>Ap.E50ESubstitution - coding silent10:131947540-131947540+
1N45-VS-1T45COSM3966958c.438T>Gp.I146MSubstitution - Missense10:131944021-131944021+
I2L-P20-Tumor-BiopsyCOSM5360065c.116G>Ap.R39HSubstitution - Missense10:131940041-131940041+
ESCC_81COSM5635839c.339_340insTCTGGp.L115fs*25Insertion - Frameshift10:131947729-131947730+
T3118COSM4717197c.58G>Ap.V20MSubstitution - Missense10:131945378-131945378+
TCGA-B5-A0K9-01COSM916287c.229C>Tp.R77WSubstitution - Missense10:131947619-131947619+
PCSI_0090_Pa_PCOSM3786635c.623A>Gp.N208SSubstitution - Missense10:131955905-131955905+
OSCC-GB_00620111COSM4881401c.110A>Gp.K37RSubstitution - Missense10:131940035-131940035+
CSCC-29-TCOSM4448153c.160C>Tp.P54SSubstitution - Missense10:131947550-131947550+
TCGA-C5-A1BE-01COSM4841483c.1063G>Ap.E355KSubstitution - Missense10:131955757-131955757+
TCGA-B5-A0K3-01COSM916296c.551A>Gp.K184RSubstitution - Missense10:131955833-131955833+
TCGA-BR-8680-01COSM4012742c.63C>Tp.F21FSubstitution - coding silent10:131945383-131945383+
YUOMEGACOSM427261c.99A>Tp.E33DSubstitution - Missense10:131934549-131934549+
TCGA-C5-A1BE-01COSM4841484c.475G>Ap.E159KSubstitution - Missense10:131955757-131955757+
TCGA-D1-A16X-01COSM916280c.340G>Ap.E114KSubstitution - Missense10:131940650-131940650+
TCGA-B0-5692-01COSM465446c.515A>Gp.D172GSubstitution - Missense10:131944098-131944098+
HCT-15COSM1675665c.1025G>Tp.R342MSubstitution - Missense10:131955719-131955719+
TCGA-BR-8680-01COSM4012741c.651C>Tp.F217FSubstitution - coding silent10:131945383-131945383+
TCGA-AP-A0LM-01COSM916292c.951C>Ap.I317ISubstitution - coding silent10:131947753-131947753+
ESCC_81COSM5635838c.927_928insTCTGGp.L311fs*25Insertion - Frameshift10:131947729-131947730+
TCGA-18-3409-01COSM683973c.1202C>Tp.P401LSubstitution - Missense10:131955896-131955896+
TCGA-66-2787-01COSM683976c.456G>Tp.T152TSubstitution - coding silent10:131955738-131955738+
PCSI_0090_Pa_PCOSM3786634c.1211A>Gp.N404SSubstitution - Missense10:131955905-131955905+
S02323COSM4387328c.23T>Cp.I8TSubstitution - Missense10:131945343-131945343+
HCC131TCOSM1603167c.118C>Tp.P40SSubstitution - Missense10:131940043-131940043+
TCGA-CD-8527-01COSM1221803c.382C>Tp.R128WSubstitution - Missense10:131940692-131940692+
TCGA-18-3409-01COSM683974c.614C>Tp.P205LSubstitution - Missense10:131955896-131955896+
TCGA-EK-A2PM-01COSM4831415c.396G>Cp.L132FSubstitution - Missense10:131943979-131943979+
WT030COSM5351944c.738G>Ap.E246ESubstitution - coding silent10:131947540-131947540+
722_TCOSM1346835c.434G>Ap.R145QSubstitution - Missense10:131944017-131944017+
TCGA-AA-A010-01COSM284195c.914G>Ap.R305HSubstitution - Missense10:131947716-131947716+
T3080COSM4717201c.500C>Tp.P167LSubstitution - Missense10:131955782-131955782+
TCGA-HQ-A2OE-01COSM1297080c.1077G>Cp.E359DSubstitution - Missense10:131955771-131955771+
EGC15COSM4012746c.455C>Tp.T152MSubstitution - Missense10:131955737-131955737+
TCGA-AP-A0LM-01COSM916282c.695G>Ap.R232HSubstitution - Missense10:131945427-131945427+
TCGA-AX-A05Z-01COSM916290c.942C>Tp.N314NSubstitution - coding silent10:131947744-131947744+
HCT-15COSM1675666c.437G>Tp.R146MSubstitution - Missense10:131955719-131955719+
TCGA-EE-A3JA-06COSM3435756c.633C>Tp.A211ASubstitution - coding silent10:131955915-131955915+
T3255COSM4717199c.294G>Ap.P98PSubstitution - coding silent10:131947684-131947684+
S02323COSM4387327c.611T>Cp.I204TSubstitution - Missense10:131945343-131945343+
I2L-P14b-Tumor-OrganoidCOSM5359886c.176T>Cp.F59SSubstitution - Missense10:131940101-131940101+
TCGA-66-2787-01COSM683975c.1044G>Tp.T348TSubstitution - coding silent10:131955738-131955738+
TCGA-HU-A4H8-01COSM4012746c.455C>Tp.T152MSubstitution - Missense10:131955737-131955737+
TCGA-CD-A4MI-01COSM4012739c.136T>Cp.Y46HSubstitution - Missense10:131940061-131940061+
TCGA-BR-4255-01COSM4012743c.870G>Ap.M290ISubstitution - Missense10:131947672-131947672+
TARGET-30-PARNNGCOSM1287345c.96G>Cp.L32LSubstitution - coding silent10:131945416-131945416+
TCGA-CG-5723-01COSM4012748c.516A>Cp.K172NSubstitution - Missense10:131955798-131955798+
TCGA-AP-A0LM-01COSM916293c.363C>Ap.I121ISubstitution - coding silent10:131947753-131947753+
TCGA-B5-A0JY-01COSM106696c.395C>Tp.S132LSubstitution - Missense10:131947785-131947785+
TCGA-EE-A3JA-06COSM3435755c.1221C>Tp.A407ASubstitution - coding silent10:131955915-131955915+
SJMB016COSM172331c.431G>Ap.R144QSubstitution - Missense10:131944014-131944014+
YUKATCOSM683974c.614C>Tp.P205LSubstitution - Missense10:131955896-131955896+
Pat_21_BCOSM916280c.340G>Ap.E114KSubstitution - Missense10:131940650-131940650+
587238COSM916282c.695G>Ap.R232HSubstitution - Missense10:131945427-131945427+
SJMB016COSM172331c.431G>Ap.R144QSubstitution - Missense10:131944014-131944014+
TCGA-BT-A3PJ-01COSM3790608c.407A>Gp.D136GSubstitution - Missense10:131943990-131943990+
LC_S31COSM1188093c.220A>Gp.I74VSubstitution - Missense10:131940145-131940145+
YUKATCOSM683973c.1202C>Tp.P401LSubstitution - Missense10:131955896-131955896+
587222COSM1221801c.1220C>Tp.A407VSubstitution - Missense10:131955914-131955914+
T3118COSM4717196c.646G>Ap.V216MSubstitution - Missense10:131945378-131945378+
TARGET-20-PAMYGX-09A-03DCOSM916286c.817C>Tp.R273WSubstitution - Missense10:131947619-131947619+
CSCC-31-TCOSM4448436c.20C>Tp.S7FSubstitution - Missense10:131934470-131934470+
TCGA-GF-A6C9-06COSM4901981c.439A>Tp.M147LSubstitution - Missense10:131955721-131955721+
TCGA-AX-A05Z-01COSM916291c.354C>Tp.N118NSubstitution - coding silent10:131947744-131947744+
TARGET-20-PAMYGX-09A-03DCOSM916287c.229C>Tp.R77WSubstitution - Missense10:131947619-131947619+
TCGA-D1-A17Q-01COSM916279c.94C>Tp.R32CSubstitution - Missense10:131934544-131934544+
T3080COSM4717200c.1088C>Tp.P363LSubstitution - Missense10:131955782-131955782+
169COSM3729975c.534delGp.G180fs*>47Deletion - Frameshift10:131955816-131955816+
SNUH_G26_S1COSM3997847c.391G>Ap.G131SSubstitution - Missense10:131947781-131947781+
9TCOSM106696c.395C>Tp.S132LSubstitution - Missense10:131947785-131947785+
587342COSM1221804c.385-1G>Tp.?Unknown10:131943967-131943967+
TCGA-AP-A0LM-01COSM916283c.107G>Ap.R36HSubstitution - Missense10:131945427-131945427+
TCGA-GF-A6C9-06COSM4901980c.1027A>Tp.M343LSubstitution - Missense10:131955721-131955721+
TCGA-AA-A010-01COSM284194c.326G>Ap.R109HSubstitution - Missense10:131947716-131947716+
084TCOSM1730966c.368G>Tp.R123MSubstitution - Missense10:131940678-131940678+
HX18TCOSM1346835c.434G>Ap.R145QSubstitution - Missense10:131944017-131944017+
PD4781aCOSM3719334c.73G>Ap.G25SSubstitution - Missense10:131934523-131934523+
587376COSM1221805c.355C>Tp.R119*Substitution - Nonsense10:131940665-131940665+
HCC07TCOSM131098c.376G>Ap.E126KSubstitution - Missense10:131947766-131947766+
TCGA-B5-A0JY-01COSM916294c.983C>Tp.S328LSubstitution - Missense10:131947785-131947785+
TCGA-HQ-A2OE-01COSM1297081c.489G>Cp.E163DSubstitution - Missense10:131955771-131955771+
S02293COSM5688376c.1046G>Ap.R349QSubstitution - Missense10:131955740-131955740+
TCGA-AA-3966-01COSM273144c.817C>Ap.R273RSubstitution - coding silent10:131947619-131947619+
TCGA-AN-A0XU-01COSM427261c.99A>Tp.E33DSubstitution - Missense10:131934549-131934549+
sysucc-1370TCOSM5469370c.1092C>Tp.R364RSubstitution - coding silent10:131955786-131955786+
587238COSM916283c.107G>Ap.R36HSubstitution - Missense10:131945427-131945427+
STC252COSM5050022c.454A>Gp.T152ASubstitution - Missense10:131944037-131944037+
I2L-P14b-Tumor-BiopsyCOSM5359886c.176T>Cp.F59SSubstitution - Missense10:131940101-131940101+
TCGA-AA-3966-01COSM273143c.229C>Ap.R77RSubstitution - coding silent10:131947619-131947619+
CSCC-40-TCOSM4589575c.205_206insAp.I71fs*2Insertion - Frameshift10:131940130-131940131+
EGC15COSM284195c.914G>Ap.R305HSubstitution - Missense10:131947716-131947716+
587222COSM1221802c.632C>Tp.A211VSubstitution - Missense10:131955914-131955914+
TCGA-BR-4255-01COSM4012744c.282G>Ap.M94ISubstitution - Missense10:131947672-131947672+
CSCC-29-TCOSM4448152c.748C>Tp.P250SSubstitution - Missense10:131947550-131947550+
ICC013TCOSM5814162c.533G>Tp.W178LSubstitution - Missense10:131944116-131944116+
TCGA-HU-A4H8-01COSM4012745c.1043C>Tp.T348MSubstitution - Missense10:131955737-131955737+
TCGA-D1-A17T-01COSM916278c.25G>Ap.V9ISubstitution - Missense10:131934475-131934475+
CSCC-27-TCOSM1221805c.355C>Tp.R119*Substitution - Nonsense10:131940665-131940665+
HCC131COSM1603167c.118C>Tp.P40SSubstitution - Missense10:131940043-131940043+
SNUH_G26_S1COSM3997846c.979G>Ap.G327SSubstitution - Missense10:131947781-131947781+
TCGA-D1-A0ZS-01COSM916289c.256T>Gp.S86ASubstitution - Missense10:131947646-131947646+
T3255COSM4717198c.882G>Ap.P294PSubstitution - coding silent10:131947684-131947684+
587284COSM1221803c.382C>Tp.R128WSubstitution - Missense10:131940692-131940692+
TCGA-C5-A1ML-01COSM4837482c.521G>Tp.R174ISubstitution - Missense10:131944104-131944104+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.380358;Hs.380362;Hs.38037210q26.36139922405432|CGAP|BC047379|C/G|non-coding||1881|Validated;
2405432|CGAP|BC072402|C/G|non-coding||1197|Validated
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.D136Gc.407A>G10133757494BLCA
AGMissensep.Y337Cc.1010A>G10133769208HNSC
AGSynonymousp.T2Tc.6A>G10133747960STAD
ATMissensep.E33Dc.99A>T10133748053BRCA
CGMissensep.L86Vc.256C>G10133753685HNSC
CTMissensep.R273Wc.817C>T10133761123UCEC
CTNonsensep.R145*c.433C>T10133757520STAD
CTSynonymousp.A407Ac.1221C>T10133769419CM
CTSynonymousp.G24Gc.72C>T10133748026LGG
GAMissensep.G335Ec.1004G>A10133769202HNSC
GAMissensep.M290Ic.870G>A10133761176STAD
GAMissensep.R227Hc.680G>A10133758916HNSC
GAMissensep.R227Hc.680G>A10133758916LUAD
GAMissensep.V9Ic.25G>A10133747979UCEC
GASynonymousp.L228Lc.684G>A10133758920LUAD
GCMissensep.E359Dc.1077G>C10133769275BLCA
GCSynonymousp.L228Lc.684G>C10133758920NB
GTSynonymousp.T348Tc.1044G>T10133769242LUSC
TGMissensep.I146Mc.438T>G10133757525LGG
TGMissensep.S282Ac.844T>G10133761150UCEC
TGSpliceDonorSNV.c.105+2T>G10133748061RCCC
TTGGMissensep.Y109Dc.324_325delinsGG10133754138CM