TOLLIP
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA1112983241298324+Missense_MutationSNPCCTTCGA-DK-A2I4-01A-11D-A21A-08TCGA-DK-A2I4-10A-01D-A21A-08g.chr11:1298324C>Tc.770G>Ac.(769-771)cGa>cAap.R257Q
BLCA1112984021298402+Missense_MutationSNPTTCTCGA-E7-A541-01A-11D-A26M-08TCGA-E7-A541-10A-01D-A26K-08g.chr11:1298402T>Cc.692A>Gc.(691-693)gAg>gGgp.E231G
BLCA1113115601311560+Missense_MutationSNPGGATCGA-XF-A9SP-01A-11D-A391-08TCGA-XF-A9SP-10A-01D-A394-08g.chr11:1311560G>Ac.263C>Tc.(262-264)aCg>aTgp.T88M
CESC1112984821298482+Splice_SiteSNPCCTTCGA-JW-A5VL-01A-11D-A28B-09TCGA-JW-A5VL-10A-01D-A28E-09g.chr11:1298482C>Tc.612G>Ac.(610-612)ggG>ggAp.G204G
COAD1112983801298380+Missense_MutationSNPCCATCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr11:1298380C>Ac.714G>Tc.(712-714)caG>caTp.Q238H
COAD1113072531307253+Missense_MutationSNPCCTTCGA-AA-A00J-01A-02W-A005-10TCGA-AA-A00J-10A-01W-A005-10g.chr11:1307253C>Tc.589G>Ac.(589-591)Gtt>Attp.V197I
COAD1113114981311498+Missense_MutationSNPGGATCGA-AA-3492-01A-01D-1408-10TCGA-AA-3492-11A-01D-1408-10g.chr11:1311498G>Ac.325C>Tc.(325-327)Ccc>Tccp.P109S
COAD1113169491316949+Missense_MutationSNPCCTTCGA-CK-4947-01B-11D-1650-10TCGA-CK-4947-10A-01D-1650-10g.chr11:1316949C>Tc.109G>Ac.(109-111)Gcc>Accp.A37T
COAD1113169841316984+Missense_MutationSNPGGATCGA-AD-6964-01A-11D-1924-10TCGA-AD-6964-10A-01D-1924-10g.chr11:1316984G>Ac.74C>Tc.(73-75)aCg>aTgp.T25M
COADREAD1112983801298380+Missense_MutationSNPCCATCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr11:1298380C>Ac.714G>Tc.(712-714)caG>caTp.Q238H
COADREAD1113072531307253+Missense_MutationSNPCCTTCGA-AA-A00J-01A-02W-A005-10TCGA-AA-A00J-10A-01W-A005-10g.chr11:1307253C>Tc.589G>Ac.(589-591)Gtt>Attp.V197I
COADREAD1113114981311498+Missense_MutationSNPGGATCGA-AA-3492-01A-01D-1408-10TCGA-AA-3492-11A-01D-1408-10g.chr11:1311498G>Ac.325C>Tc.(325-327)Ccc>Tccp.P109S
COADREAD1113169491316949+Missense_MutationSNPCCTTCGA-CK-4947-01B-11D-1650-10TCGA-CK-4947-10A-01D-1650-10g.chr11:1316949C>Tc.109G>Ac.(109-111)Gcc>Accp.A37T
COADREAD1113169841316984+Missense_MutationSNPGGATCGA-AD-6964-01A-11D-1924-10TCGA-AD-6964-10A-01D-1924-10g.chr11:1316984G>Ac.74C>Tc.(73-75)aCg>aTgp.T25M
ESCA1113072981307298+Missense_MutationSNPGGATCGA-JY-A6FD-01A-11D-A33E-09TCGA-JY-A6FD-10A-01D-A33H-09g.chr11:1307298G>Ac.544C>Tc.(544-546)Cca>Tcap.P182S
GBMLGG1112984481298448+Missense_MutationSNPCCTTCGA-FG-A4MU-01B-11D-A289-08TCGA-FG-A4MU-10A-01D-A289-08g.chr11:1298448C>Tc.646G>Ac.(646-648)Gtg>Atgp.V216M
HNSC1112984221298422+SilentSNPGGATCGA-UF-A71E-01A-31D-A34J-08TCGA-UF-A71E-10B-01D-A34M-08g.chr11:1298422G>Ac.672C>Tc.(670-672)aaC>aaTp.N224N
HNSC1113098661309866+SilentSNPGGATCGA-CQ-5323-01A-01D-1683-08TCGA-CQ-5323-10A-01D-1683-08g.chr11:1309866G>Ac.507C>Tc.(505-507)gtC>gtTp.V169V
HNSC1113098681309868+Missense_MutationSNPCCTTCGA-TN-A7HL-01A-11D-A34J-08TCGA-TN-A7HL-10A-01D-A34M-08g.chr11:1309868C>Tc.505G>Ac.(505-507)Gtc>Atcp.V169I
HNSC1113100071310007+Splice_SiteSNPCCTTCGA-IQ-A61I-01A-11D-A30E-08TCGA-IQ-A61I-10A-01D-A30H-08g.chr11:1310007C>Tc.e4-1
LGG1112984481298448+Missense_MutationSNPCCTTCGA-FG-A4MU-01B-11D-A289-08TCGA-FG-A4MU-10A-01D-A289-08g.chr11:1298448C>Tc.646G>Ac.(646-648)Gtg>Atgp.V216M
LIHC1113099261309926+SilentSNPGGATCGA-GJ-A9DB-01A-11D-A36X-10TCGA-GJ-A9DB-10A-01D-A370-10g.chr11:1309926G>Ac.447C>Tc.(445-447)gaC>gaTp.D149D
LUAD1112983281298328+Missense_MutationSNPGGTTCGA-44-3918-01A-01D-1105-08TCGA-44-3918-11A-01D-1105-08g.chr11:1298328G>Tc.766C>Ac.(766-768)Cag>Aagp.Q256K
LUAD1112984611298461+SilentSNPGGATCGA-L9-A444-01A-21D-A24D-08TCGA-L9-A444-10A-01D-A24F-08g.chr11:1298461G>Ac.633C>Tc.(631-633)ccC>ccTp.P211P
LUAD1113114911311491+Missense_MutationSNPCCTTCGA-53-7624-01A-11D-2063-08TCGA-53-7624-10A-01D-2063-08g.chr11:1311491C>Tc.332G>Ac.(331-333)gGc>gAcp.G111D
LUAD1113168781316878+SilentSNPTTCTCGA-91-6831-01A-11D-1855-08TCGA-91-6831-11A-02D-1855-08g.chr11:1316878T>Cc.180A>Gc.(178-180)gtA>gtGp.V60V
LUSC1113116181311618+Missense_MutationSNPCCTTCGA-18-3406-01A-01D-0983-08TCGA-18-3406-11A-01D-0983-08g.chr11:1311618C>Tc.205G>Ac.(205-207)Ggc>Agcp.G69S
SARC1113115711311571+SilentSNPCCTTCGA-UE-A6QU-01A-12D-A32I-09TCGA-UE-A6QU-10B-01D-A32I-09g.chr11:1311571C>Tc.252G>Ac.(250-252)gcG>gcAp.A84A
SKCM1113115301311530+Missense_MutationSNPGGATCGA-EE-A29E-06A-11D-A197-08TCGA-EE-A29E-10A-01D-A199-08g.chr11:1311530G>Ac.293C>Tc.(292-294)cCc>cTcp.P98L
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US1112983241298324single base substitutionCT3_prime_UTR_variant
BLCA-US1112983241298324single base substitutionCTdownstream_gene_variant
BLCA-US1112983241298324single base substitutionCTmissense_variantR188Q563G>A
BLCA-US1112983241298324single base substitutionCTmissense_variantR196Q587G>A
BLCA-US1112983241298324single base substitutionCTmissense_variantR207Q620G>A
BLCA-US1112983241298324single base substitutionCTmissense_variantR229Q686G>A
BLCA-US1112983241298324single base substitutionCTmissense_variantR257Q770G>A
BOCA-FR1113154881315488single base substitutionAGdownstream_gene_variant
BOCA-FR1113154881315488single base substitutionAGintron_variant
BOCA-FR1113154881315488single base substitutionAGupstream_gene_variant
BOCA-FR1113265471326547single base substitutionGAintron_variant
BOCA-FR1113265471326547single base substitutionGAupstream_gene_variant
BRCA-EU1112914121291412single base substitutionGAdownstream_gene_variant
BRCA-EU1112918291291829single base substitutionCTdownstream_gene_variant
BRCA-EU1112927561292756single base substitutionCGdownstream_gene_variant
BRCA-EU1112935991293599deletion of <=200bpC-downstream_gene_variant
BRCA-EU1112958671295867single base substitutionCT3_prime_UTR_variant
BRCA-EU1112958671295867single base substitutionCTdownstream_gene_variant
BRCA-EU1113029341302934single base substitutionCTintron_variant
BRCA-EU1113044761304476single base substitutionCTintron_variant
BRCA-EU1113067611306761insertion of <=200bp-Cdownstream_gene_variant
BRCA-EU1113067611306761insertion of <=200bp-Cintron_variant
BRCA-EU1113080031308003single base substitutionTCdownstream_gene_variant
BRCA-EU1113080031308003single base substitutionTCintron_variant
BRCA-EU1113130921313092single base substitutionCTdownstream_gene_variant
BRCA-EU1113130921313092single base substitutionCTexon_variant
BRCA-EU1113130921313092single base substitutionCTintron_variant
BRCA-EU1113136881313688single base substitutionGAdownstream_gene_variant
BRCA-EU1113136881313688single base substitutionGAintron_variant
BRCA-EU1113136881313688single base substitutionGAupstream_gene_variant
BRCA-EU1113141041314104single base substitutionGAdownstream_gene_variant
BRCA-EU1113141041314104single base substitutionGAintron_variant
BRCA-EU1113141041314104single base substitutionGAupstream_gene_variant
BRCA-EU1113155621315562single base substitutionCTdownstream_gene_variant
BRCA-EU1113155621315562single base substitutionCTintron_variant
BRCA-EU1113155621315562single base substitutionCTupstream_gene_variant
BRCA-EU1113163291316329single base substitutionATdownstream_gene_variant
BRCA-EU1113163291316329single base substitutionATintron_variant
BRCA-EU1113163291316329single base substitutionATupstream_gene_variant
BRCA-EU1113193471319347single base substitutionGCdownstream_gene_variant
BRCA-EU1113193471319347single base substitutionGCintron_variant
BRCA-EU1113195461319546single base substitutionCGexon_variant
BRCA-EU1113195461319546single base substitutionCGintron_variant
BRCA-EU1113205861320586single base substitutionGCintron_variant
BRCA-EU1113209191320919single base substitutionCGintron_variant
BRCA-EU1113211531321153single base substitutionCTintron_variant
BRCA-EU1113221301322130single base substitutionCGintron_variant
BRCA-EU1113221481322148single base substitutionGAintron_variant
BRCA-EU1113221881322188single base substitutionCTintron_variant
BRCA-EU1113228411322841single base substitutionGAintron_variant
BRCA-EU1113262191326219single base substitutionCTintron_variant
BRCA-EU1113262191326219single base substitutionCTupstream_gene_variant
BRCA-EU1113273981327398single base substitutionGAexon_variant
BRCA-EU1113273981327398single base substitutionGAintron_variant
BRCA-EU1113273981327398single base substitutionGAupstream_gene_variant
BRCA-EU1113277721327772single base substitutionGAintron_variant
BRCA-EU1113277721327772single base substitutionGAupstream_gene_variant
BRCA-EU1113282941328294single base substitutionCTintron_variant
BRCA-EU1113282941328294single base substitutionCTupstream_gene_variant
BRCA-EU1113294111329411single base substitutionGAintron_variant
BRCA-EU1113294111329411single base substitutionGAupstream_gene_variant
BRCA-EU1113298751329875single base substitutionAGintron_variant
BRCA-EU1113298751329875single base substitutionAGupstream_gene_variant
BRCA-EU1113310001331000single base substitutionCGupstream_gene_variant
BRCA-EU1113337481333748insertion of <=200bp-Aupstream_gene_variant
BRCA-EU1113337561333756single base substitutionTAupstream_gene_variant
BRCA-EU1113346721334672single base substitutionCTupstream_gene_variant
BRCA-EU1113353381335338deletion of <=200bpT-upstream_gene_variant
BRCA-EU1113355651335565single base substitutionTCupstream_gene_variant
BRCA-FR1112958671295867single base substitutionCT3_prime_UTR_variant
BRCA-FR1112958671295867single base substitutionCTdownstream_gene_variant
BRCA-FR1113029341302934single base substitutionCTintron_variant
BRCA-UK1113221881322188single base substitutionCTintron_variant
BRCA-UK1113223271322327single base substitutionGAintron_variant
BRCA-UK1113233721323372single base substitutionCTintron_variant
BRCA-UK1113322771332277single base substitutionGCupstream_gene_variant
BTCA-JP1112984831298483single base substitutionCAmissense_variantG135V404G>T
BTCA-JP1112984831298483single base substitutionCAmissense_variantG143V428G>T
BTCA-JP1112984831298483single base substitutionCAmissense_variantG154V461G>T
BTCA-JP1112984831298483single base substitutionCAmissense_variantG176V527G>T
BTCA-JP1112984831298483single base substitutionCAmissense_variantG204V611G>T
BTCA-JP1112984831298483single base substitutionCAsplice_region_variant
BTCA-JP1112984831298483single base substitutionCAstop_gainedG62*184G>T
BTCA-JP1113047181304718single base substitutionGA3_prime_UTR_variant
BTCA-JP1113047181304718single base substitutionGAintron_variant
CESC-US1112984821298482single base substitutionCTmissense_variantG62E185G>A
CESC-US1112984821298482single base substitutionCTsplice_region_variant
CLLE-ES1112957721295772single base substitutionAG3_prime_UTR_variant
CLLE-ES1112957721295772single base substitutionAGdownstream_gene_variant
CLLE-ES1113046281304628single base substitutionCT3_prime_UTR_variant
CLLE-ES1113046281304628single base substitutionCTintron_variant
COAD-US1112983801298380single base substitutionCA3_prime_UTR_variant
COAD-US1112983801298380single base substitutionCAdownstream_gene_variant
COAD-US1112983801298380single base substitutionCAmissense_variantQ169H507G>T
COAD-US1112983801298380single base substitutionCAmissense_variantQ177H531G>T
COAD-US1112983801298380single base substitutionCAmissense_variantQ188H564G>T
COAD-US1112983801298380single base substitutionCAmissense_variantQ210H630G>T
COAD-US1112983801298380single base substitutionCAmissense_variantQ238H714G>T
COAD-US1113114981311498single base substitutionGAdownstream_gene_variant
COAD-US1113114981311498single base substitutionGAexon_variant
COAD-US1113114981311498single base substitutionGAintron_variant
COAD-US1113114981311498single base substitutionGAmissense_variantP109S325C>T
COAD-US1113114981311498single base substitutionGAmissense_variantP40S118C>T
COAD-US1113114981311498single base substitutionGAmissense_variantP59S175C>T
COAD-US1113114981311498single base substitutionGAmissense_variantP81S241C>T
COAD-US1113169491316949single base substitutionCT5_prime_UTR_variant
COAD-US1113169491316949single base substitutionCTdownstream_gene_variant
COAD-US1113169491316949single base substitutionCTexon_variant
COAD-US1113169491316949single base substitutionCTintron_variant
COAD-US1113169491316949single base substitutionCTmissense_variantA37T109G>A
COAD-US1113169491316949single base substitutionCTmissense_variantA9T25G>A
COAD-US1113169491316949single base substitutionCTupstream_gene_variant
COAD-US1113169841316984single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
COAD-US1113169841316984single base substitutionGAdownstream_gene_variant
COAD-US1113169841316984single base substitutionGAexon_variant
COAD-US1113169841316984single base substitutionGAintron_variant
COAD-US1113169841316984single base substitutionGAmissense_variantT25M74C>T
COAD-US1113169841316984single base substitutionGAupstream_gene_variant
COCA-CN1113040041304004single base substitutionGAintron_variant
COCA-CN1113041061304106single base substitutionTCintron_variant
COCA-CN1113042871304287single base substitutionCGintron_variant
COCA-CN1113080031308003single base substitutionTCdownstream_gene_variant
COCA-CN1113080031308003single base substitutionTCintron_variant
COCA-CN1113080401308040single base substitutionCTdownstream_gene_variant
COCA-CN1113080401308040single base substitutionCTintron_variant
COCA-CN1113106551310655single base substitutionGAdownstream_gene_variant
COCA-CN1113106551310655single base substitutionGAintron_variant
COCA-CN1113115901311590single base substitutionCTdownstream_gene_variant
COCA-CN1113115901311590single base substitutionCTexon_variant
COCA-CN1113115901311590single base substitutionCTintron_variant
COCA-CN1113115901311590single base substitutionCTmissense_variantR28Q83G>A
COCA-CN1113115901311590single base substitutionCTmissense_variantR50Q149G>A
COCA-CN1113115901311590single base substitutionCTmissense_variantR78Q233G>A
COCA-CN1113115901311590single base substitutionCTmissense_variantR9Q26G>A
COCA-CN1113130541313054single base substitutionACdownstream_gene_variant
COCA-CN1113130541313054single base substitutionACintron_variant
COCA-CN1113130541313054single base substitutionACsplice_donor_variant
COCA-CN1113279621327962single base substitutionCTintron_variant
COCA-CN1113279621327962single base substitutionCTupstream_gene_variant
COCA-CN1113291391329139single base substitutionAGintron_variant
COCA-CN1113291391329139single base substitutionAGupstream_gene_variant
EOPC-DE1112918741291874single base substitutionGAdownstream_gene_variant
EOPC-DE1112998201299820single base substitutionACintron_variant
EOPC-DE1113080981308098single base substitutionAGdownstream_gene_variant
EOPC-DE1113080981308098single base substitutionAGintron_variant
EOPC-DE1113108561310856single base substitutionCTdownstream_gene_variant
EOPC-DE1113108561310856single base substitutionCTintron_variant
EOPC-DE1113121211312121single base substitutionCTdownstream_gene_variant
EOPC-DE1113121211312121single base substitutionCTintron_variant
EOPC-DE1113127581312758single base substitutionACdownstream_gene_variant
EOPC-DE1113127581312758single base substitutionACintron_variant
EOPC-DE1113130541313054single base substitutionACdownstream_gene_variant
EOPC-DE1113130541313054single base substitutionACintron_variant
EOPC-DE1113130541313054single base substitutionACsplice_donor_variant
EOPC-DE1113281161328116single base substitutionACintron_variant
EOPC-DE1113281161328116single base substitutionACupstream_gene_variant
ESAD-UK1112918711291871single base substitutionGAdownstream_gene_variant
ESAD-UK1112937721293772single base substitutionCTdownstream_gene_variant
ESAD-UK1112939191293919single base substitutionGAdownstream_gene_variant
ESAD-UK1112943971294397single base substitutionCTdownstream_gene_variant
ESAD-UK1112954761295476single base substitutionCTdownstream_gene_variant
ESAD-UK1112959971295997single base substitutionAC3_prime_UTR_variant
ESAD-UK1112959971295997single base substitutionACdownstream_gene_variant
ESAD-UK1113013801301380single base substitutionGAintron_variant
ESAD-UK1113017761301776single base substitutionCTintron_variant
ESAD-UK1113035711303571single base substitutionGAintron_variant
ESAD-UK1113042271304227single base substitutionGAintron_variant
ESAD-UK1113068031306803single base substitutionATdownstream_gene_variant
ESAD-UK1113068031306803single base substitutionATintron_variant
ESAD-UK1113095611309561single base substitutionCTdownstream_gene_variant
ESAD-UK1113095611309561single base substitutionCTintron_variant
ESAD-UK1113110511311051single base substitutionGAdownstream_gene_variant
ESAD-UK1113110511311051single base substitutionGAintron_variant
ESAD-UK1113111661311166single base substitutionGAdownstream_gene_variant
ESAD-UK1113111661311166single base substitutionGAintron_variant
ESAD-UK1113114011311401single base substitutionCTdownstream_gene_variant
ESAD-UK1113114011311401single base substitutionCTexon_variant
ESAD-UK1113114011311401single base substitutionCTintron_variant
ESAD-UK1113126841312684single base substitutionCAdownstream_gene_variant
ESAD-UK1113126841312684single base substitutionCAintron_variant
ESAD-UK1113164411316441single base substitutionCTdownstream_gene_variant
ESAD-UK1113164411316441single base substitutionCTintron_variant
ESAD-UK1113164411316441single base substitutionCTupstream_gene_variant
ESAD-UK1113182821318282single base substitutionAGdownstream_gene_variant
ESAD-UK1113182821318282single base substitutionAGintron_variant
ESAD-UK1113182821318282single base substitutionAGupstream_gene_variant
ESAD-UK1113197261319726single base substitutionCTexon_variant
ESAD-UK1113197261319726single base substitutionCTintron_variant
ESAD-UK1113258951325895single base substitutionGCintron_variant
ESAD-UK1113258951325895single base substitutionGCupstream_gene_variant
ESAD-UK1113260021326002single base substitutionTCintron_variant
ESAD-UK1113260021326002single base substitutionTCupstream_gene_variant
ESAD-UK1113291581329158single base substitutionCGintron_variant
ESAD-UK1113291581329158single base substitutionCGupstream_gene_variant
ESAD-UK1113307881330788single base substitutionGA5_prime_UTR_variant
ESAD-UK1113307881330788single base substitutionGAexon_variant
ESAD-UK1113307881330788single base substitutionGAupstream_gene_variant
ESAD-UK1113340801334080single base substitutionGAupstream_gene_variant
ESAD-UK1113355781335578single base substitutionTCupstream_gene_variant
ESCA-CN1113097801309780single base substitutionCTdownstream_gene_variant
ESCA-CN1113097801309780single base substitutionCTintron_variant
LAML-KR1113036661303666single base substitutionAGintron_variant
LAML-KR1113038491303849single base substitutionAGintron_variant
LAML-KR1113038591303859single base substitutionGAintron_variant
LAML-KR1113041061304106single base substitutionTCintron_variant
LAML-KR1113080031308003single base substitutionTCdownstream_gene_variant
LAML-KR1113080031308003single base substitutionTCintron_variant
LAML-KR1113080401308040single base substitutionCTdownstream_gene_variant
LAML-KR1113080401308040single base substitutionCTintron_variant
LAML-KR1113111741311174single base substitutionAGdownstream_gene_variant
LAML-KR1113111741311174single base substitutionAGintron_variant
LAML-KR1113156871315687single base substitutionCTdownstream_gene_variant
LAML-KR1113156871315687single base substitutionCTintron_variant
LAML-KR1113156871315687single base substitutionCTupstream_gene_variant
LAML-KR1113157341315734single base substitutionCTdownstream_gene_variant
LAML-KR1113157341315734single base substitutionCTintron_variant
LAML-KR1113157341315734single base substitutionCTupstream_gene_variant
LAML-KR1113162041316204single base substitutionCTdownstream_gene_variant
LAML-KR1113162041316204single base substitutionCTintron_variant
LAML-KR1113162041316204single base substitutionCTupstream_gene_variant
LAML-KR1113178011317801single base substitutionATdownstream_gene_variant
LAML-KR1113178011317801single base substitutionATintron_variant
LAML-KR1113178011317801single base substitutionATupstream_gene_variant
LAML-KR1113181831318183single base substitutionTAdownstream_gene_variant
LAML-KR1113181831318183single base substitutionTAintron_variant
LAML-KR1113181831318183single base substitutionTAupstream_gene_variant
LGG-US1112984481298448single base substitutionCT3_prime_UTR_variant
LGG-US1112984481298448single base substitutionCTmissense_variantV147M439G>A
LGG-US1112984481298448single base substitutionCTmissense_variantV155M463G>A
LGG-US1112984481298448single base substitutionCTmissense_variantV166M496G>A
LGG-US1112984481298448single base substitutionCTmissense_variantV188M562G>A
LGG-US1112984481298448single base substitutionCTmissense_variantV216M646G>A
LGG-US1112984481298448single base substitutionCTsynonymous_variantP73P219G>A
LICA-FR1113098551309855single base substitutionGAdownstream_gene_variant
LICA-FR1113098551309855single base substitutionGAintron_variant
LICA-FR1113098551309855single base substitutionGAmissense_variantA104V311C>T
LICA-FR1113098551309855single base substitutionGAmissense_variantA112V335C>T
LICA-FR1113098551309855single base substitutionGAmissense_variantA123V368C>T
LICA-FR1113098551309855single base substitutionGAmissense_variantA145V434C>T
LICA-FR1113098551309855single base substitutionGAmissense_variantA173V518C>T
LICA-FR1113098551309855single base substitutionGAsplice_region_variant
LICA-FR1113157551315755single base substitutionCTdownstream_gene_variant
LICA-FR1113157551315755single base substitutionCTintron_variant
LICA-FR1113157551315755single base substitutionCTupstream_gene_variant
LICA-FR1113162251316225single base substitutionCTdownstream_gene_variant
LICA-FR1113162251316225single base substitutionCTintron_variant
LICA-FR1113162251316225single base substitutionCTupstream_gene_variant
LICA-FR1113169411316941single base substitutionCT5_prime_UTR_variant
LICA-FR1113169411316941single base substitutionCTdownstream_gene_variant
LICA-FR1113169411316941single base substitutionCTexon_variant
LICA-FR1113169411316941single base substitutionCTintron_variant
LICA-FR1113169411316941single base substitutionCTsynonymous_variantA11A33G>A
LICA-FR1113169411316941single base substitutionCTsynonymous_variantA39A117G>A
LICA-FR1113169411316941single base substitutionCTupstream_gene_variant
LINC-JP1112983161298316single base substitutionTC3_prime_UTR_variant
LINC-JP1112983161298316single base substitutionTCdownstream_gene_variant
LINC-JP1112983161298316single base substitutionTCmissense_variantK191E571A>G
LINC-JP1112983161298316single base substitutionTCmissense_variantK199E595A>G
LINC-JP1112983161298316single base substitutionTCmissense_variantK210E628A>G
LINC-JP1112983161298316single base substitutionTCmissense_variantK232E694A>G
LINC-JP1112983161298316single base substitutionTCmissense_variantK260E778A>G
LINC-JP1112986021298602single base substitutionCTintron_variant
LINC-JP1113040611304061single base substitutionCTintron_variant
LINC-JP1113048811304881single base substitutionACdownstream_gene_variant
LINC-JP1113048811304881single base substitutionACintron_variant
LINC-JP1113048891304889single base substitutionCTdownstream_gene_variant
LINC-JP1113048891304889single base substitutionCTintron_variant
LINC-JP1113102241310224single base substitutionTCdownstream_gene_variant
LINC-JP1113102241310224single base substitutionTCintron_variant
LINC-JP1113249071324907single base substitutionTGintron_variant
LINC-JP1113249071324907single base substitutionTGupstream_gene_variant
LINC-JP1113300941330094insertion of <=200bp-Cintron_variant
LINC-JP1113300941330094insertion of <=200bp-Cupstream_gene_variant
LINC-JP1113300991330099deletion of <=200bpC-intron_variant
LINC-JP1113300991330099deletion of <=200bpC-upstream_gene_variant
LINC-JP1113301121330112deletion of <=200bpG-intron_variant
LINC-JP1113301121330112deletion of <=200bpG-upstream_gene_variant
LIRI-JP1112975171297517single base substitutionAT3_prime_UTR_variant
LIRI-JP1112975171297517single base substitutionATdownstream_gene_variant
LIRI-JP1112976501297650single base substitutionTA3_prime_UTR_variant
LIRI-JP1112976501297650single base substitutionTAdownstream_gene_variant
LIRI-JP1113009941300994single base substitutionTCintron_variant
LIRI-JP1113060611306061single base substitutionGAdownstream_gene_variant
LIRI-JP1113060611306061single base substitutionGAintron_variant
LIRI-JP1113072661307266single base substitutionCTdownstream_gene_variant
LIRI-JP1113072661307266single base substitutionCTexon_variant
LIRI-JP1113072661307266single base substitutionCTintron_variant
LIRI-JP1113072661307266single base substitutionCTsynonymous_variantV123V369G>A
LIRI-JP1113072661307266single base substitutionCTsynonymous_variantV131V393G>A
LIRI-JP1113072661307266single base substitutionCTsynonymous_variantV142V426G>A
LIRI-JP1113072661307266single base substitutionCTsynonymous_variantV164V492G>A
LIRI-JP1113072661307266single base substitutionCTsynonymous_variantV192V576G>A
LIRI-JP1113102091310210deletion of <=200bpCT-downstream_gene_variant
LIRI-JP1113102091310210deletion of <=200bpCT-intron_variant
LIRI-JP1113150431315043single base substitutionTCdownstream_gene_variant
LIRI-JP1113150431315043single base substitutionTCintron_variant
LIRI-JP1113150431315043single base substitutionTCupstream_gene_variant
LIRI-JP1113188741318874single base substitutionCAdownstream_gene_variant
LIRI-JP1113188741318874single base substitutionCAintron_variant
LIRI-JP1113217891321789single base substitutionTAintron_variant
LIRI-JP1113218521321852single base substitutionGCintron_variant
LIRI-JP1113223421322342single base substitutionTCintron_variant
LIRI-JP1113224231322423single base substitutionATintron_variant
LIRI-JP1113241381324138deletion of <=200bpG-intron_variant
LIRI-JP1113241381324138deletion of <=200bpG-upstream_gene_variant
LIRI-JP1113251021325102single base substitutionCAintron_variant
LIRI-JP1113251021325102single base substitutionCAupstream_gene_variant
LIRI-JP1113274001327400single base substitutionACexon_variant
LIRI-JP1113274001327400single base substitutionACintron_variant
LIRI-JP1113274001327400single base substitutionACupstream_gene_variant
LIRI-JP1113299281329928single base substitutionGAintron_variant
LIRI-JP1113299281329928single base substitutionGAupstream_gene_variant
LIRI-JP1113323641332364single base substitutionTCupstream_gene_variant
LIRI-JP1113334401333440single base substitutionAGupstream_gene_variant
LIRI-JP1113354571335457single base substitutionACupstream_gene_variant
LUSC-KR1113036661303666single base substitutionAGintron_variant
LUSC-KR1113036701303670single base substitutionCTintron_variant
LUSC-KR1113038491303849single base substitutionAGintron_variant
LUSC-KR1113039291303929single base substitutionGCintron_variant
LUSC-KR1113073731307373single base substitutionCTdownstream_gene_variant
LUSC-KR1113073731307373single base substitutionCTintron_variant
LUSC-KR1113126231312623single base substitutionCTdownstream_gene_variant
LUSC-KR1113126231312623single base substitutionCTintron_variant
LUSC-KR1113153781315378single base substitutionAGdownstream_gene_variant
LUSC-KR1113153781315378single base substitutionAGintron_variant
LUSC-KR1113153781315378single base substitutionAGupstream_gene_variant
LUSC-KR1113154311315431single base substitutionTCdownstream_gene_variant
LUSC-KR1113154311315431single base substitutionTCintron_variant
LUSC-KR1113154311315431single base substitutionTCupstream_gene_variant
LUSC-KR1113156541315654single base substitutionCTdownstream_gene_variant
LUSC-KR1113156541315654single base substitutionCTintron_variant
LUSC-KR1113156541315654single base substitutionCTupstream_gene_variant
LUSC-KR1113162721316272single base substitutionTCdownstream_gene_variant
LUSC-KR1113162721316272single base substitutionTCintron_variant
LUSC-KR1113162721316272single base substitutionTCupstream_gene_variant
LUSC-KR1113176791317679single base substitutionCGdownstream_gene_variant
LUSC-KR1113176791317679single base substitutionCGintron_variant
LUSC-KR1113176791317679single base substitutionCGupstream_gene_variant
LUSC-KR1113178011317801single base substitutionATdownstream_gene_variant
LUSC-KR1113178011317801single base substitutionATintron_variant
LUSC-KR1113178011317801single base substitutionATupstream_gene_variant
LUSC-KR1113179591317959single base substitutionATdownstream_gene_variant
LUSC-KR1113179591317959single base substitutionATintron_variant
LUSC-KR1113179591317959single base substitutionATupstream_gene_variant
LUSC-KR1113182391318239single base substitutionTAdownstream_gene_variant
LUSC-KR1113182391318239single base substitutionTAintron_variant
LUSC-KR1113182391318239single base substitutionTAupstream_gene_variant
LUSC-KR1113205051320505single base substitutionTCintron_variant
LUSC-KR1113256971325697single base substitutionGAintron_variant
LUSC-KR1113256971325697single base substitutionGAupstream_gene_variant
LUSC-KR1113281121328112single base substitutionTCintron_variant
LUSC-KR1113281121328112single base substitutionTCupstream_gene_variant
LUSC-KR1113300781330078single base substitutionGTintron_variant
LUSC-KR1113300781330078single base substitutionGTupstream_gene_variant
LUSC-KR1113300871330087single base substitutionCAintron_variant
LUSC-KR1113300871330087single base substitutionCAupstream_gene_variant
LUSC-KR1113322071332207single base substitutionGAupstream_gene_variant
LUSC-US1113116181311618single base substitutionCT5_prime_UTR_variant
LUSC-US1113116181311618single base substitutionCTdownstream_gene_variant
LUSC-US1113116181311618single base substitutionCTexon_variant
LUSC-US1113116181311618single base substitutionCTintron_variant
LUSC-US1113116181311618single base substitutionCTmissense_variantG19S55G>A
LUSC-US1113116181311618single base substitutionCTmissense_variantG41S121G>A
LUSC-US1113116181311618single base substitutionCTmissense_variantG69S205G>A
MALY-DE1112918151291815single base substitutionGTdownstream_gene_variant
MALY-DE1112931301293130insertion of <=200bp-Cdownstream_gene_variant
MALY-DE1113111701311170single base substitutionGAdownstream_gene_variant
MALY-DE1113111701311170single base substitutionGAintron_variant
MALY-DE1113168051316805single base substitutionCAdownstream_gene_variant
MALY-DE1113168051316805single base substitutionCAexon_variant
MALY-DE1113168051316805single base substitutionCAintron_variant
MALY-DE1113168051316805single base substitutionCAupstream_gene_variant
MALY-DE1113207401320740single base substitutionGAintron_variant
MALY-DE1113353381335338deletion of <=200bpT-upstream_gene_variant
MELA-AU1112906781290678single base substitutionGAdownstream_gene_variant
MELA-AU1112912061291206single base substitutionGAdownstream_gene_variant
MELA-AU1112915251291525single base substitutionGAdownstream_gene_variant
MELA-AU1112917011291701single base substitutionGCdownstream_gene_variant
MELA-AU1112918081291808single base substitutionGAdownstream_gene_variant
MELA-AU1112919331291933single base substitutionGAdownstream_gene_variant
MELA-AU1112920191292026deletion of <=200bpTCCAGAAC-downstream_gene_variant
MELA-AU1112923921292392single base substitutionGAdownstream_gene_variant
MELA-AU1112931961293196single base substitutionGAdownstream_gene_variant
MELA-AU1112932051293205single base substitutionGAdownstream_gene_variant
MELA-AU1112933021293302single base substitutionGAdownstream_gene_variant
MELA-AU1112937501293750single base substitutionCTdownstream_gene_variant
MELA-AU1112939421293943multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU1112947871294787single base substitutionGCdownstream_gene_variant
MELA-AU1112948981294898single base substitutionCGdownstream_gene_variant
MELA-AU1112949571294957single base substitutionGAdownstream_gene_variant
MELA-AU1112952661295266single base substitutionGAdownstream_gene_variant
MELA-AU1112958021295802single base substitutionGA3_prime_UTR_variant
MELA-AU1112958021295802single base substitutionGAdownstream_gene_variant
MELA-AU1112959091295909single base substitutionGA3_prime_UTR_variant
MELA-AU1112959091295909single base substitutionGAdownstream_gene_variant
MELA-AU1112960101296010single base substitutionAG3_prime_UTR_variant
MELA-AU1112960101296010single base substitutionAGdownstream_gene_variant
MELA-AU1112961101296110single base substitutionGA3_prime_UTR_variant
MELA-AU1112961101296110single base substitutionGAdownstream_gene_variant
MELA-AU1112963111296311single base substitutionGA3_prime_UTR_variant
MELA-AU1112963111296311single base substitutionGAdownstream_gene_variant
MELA-AU1112967161296716single base substitutionGA3_prime_UTR_variant
MELA-AU1112967161296716single base substitutionGAdownstream_gene_variant
MELA-AU1112969461296946single base substitutionCT3_prime_UTR_variant
MELA-AU1112969461296946single base substitutionCTdownstream_gene_variant
MELA-AU1112982961298296single base substitutionGA3_prime_UTR_variant
MELA-AU1112982961298296single base substitutionGAdownstream_gene_variant
MELA-AU1112982961298296single base substitutionGAsynonymous_variantS197S591C>T
MELA-AU1112982961298296single base substitutionGAsynonymous_variantS205S615C>T
MELA-AU1112982961298296single base substitutionGAsynonymous_variantS216S648C>T
MELA-AU1112982961298296single base substitutionGAsynonymous_variantS238S714C>T
MELA-AU1112982961298296single base substitutionGAsynonymous_variantS266S798C>T
MELA-AU1112984291298429single base substitutionGA3_prime_UTR_variant
MELA-AU1112984291298429single base substitutionGAmissense_variantA153V458C>T
MELA-AU1112984291298429single base substitutionGAmissense_variantA161V482C>T
MELA-AU1112984291298429single base substitutionGAmissense_variantA172V515C>T
MELA-AU1112984291298429single base substitutionGAmissense_variantA194V581C>T
MELA-AU1112984291298429single base substitutionGAmissense_variantA222V665C>T
MELA-AU1112984291298429single base substitutionGAmissense_variantP80S238C>T
MELA-AU1112994241299424single base substitutionAGintron_variant
MELA-AU1113001371300137single base substitutionGAintron_variant
MELA-AU1113010141301014single base substitutionAGintron_variant
MELA-AU1113017341301734single base substitutionGAintron_variant
MELA-AU1113018241301824single base substitutionGAintron_variant
MELA-AU1113021071302107single base substitutionGAintron_variant
MELA-AU1113021181302118single base substitutionGAintron_variant
MELA-AU1113021901302190single base substitutionTCintron_variant
MELA-AU1113027641302764single base substitutionCTintron_variant
MELA-AU1113032101303210single base substitutionTGintron_variant
MELA-AU1113037401303740single base substitutionGCintron_variant
MELA-AU1113041511304152multiple base substitution (>=2bp and <=200bp)AACTintron_variant
MELA-AU1113045551304555single base substitutionGA3_prime_UTR_variant
MELA-AU1113045551304555single base substitutionGAintron_variant
MELA-AU1113047651304765single base substitutionTAexon_variant
MELA-AU1113047651304765single base substitutionTAintron_variant
MELA-AU1113050101305010single base substitutionGAdownstream_gene_variant
MELA-AU1113050101305010single base substitutionGAintron_variant
MELA-AU1113050701305070single base substitutionGAdownstream_gene_variant
MELA-AU1113050701305070single base substitutionGAintron_variant
MELA-AU1113060431306043deletion of <=200bpA-downstream_gene_variant
MELA-AU1113060431306043deletion of <=200bpA-intron_variant
MELA-AU1113065101306510single base substitutionCTdownstream_gene_variant
MELA-AU1113065101306510single base substitutionCTintron_variant
MELA-AU1113070351307035single base substitutionAGdownstream_gene_variant
MELA-AU1113070351307035single base substitutionAGintron_variant
MELA-AU1113096201309620single base substitutionAGdownstream_gene_variant
MELA-AU1113096201309620single base substitutionAGintron_variant
MELA-AU1113101111310111single base substitutionGAdownstream_gene_variant
MELA-AU1113101111310111single base substitutionGAintron_variant
MELA-AU1113103381310338single base substitutionGAdownstream_gene_variant
MELA-AU1113103381310338single base substitutionGAintron_variant
MELA-AU1113105021310502single base substitutionGAdownstream_gene_variant
MELA-AU1113105021310502single base substitutionGAintron_variant
MELA-AU1113108691310869single base substitutionGAdownstream_gene_variant
MELA-AU1113108691310869single base substitutionGAintron_variant
MELA-AU1113118011311801single base substitutionGAdownstream_gene_variant
MELA-AU1113118011311801single base substitutionGAintron_variant
MELA-AU1113121401312140single base substitutionCTdownstream_gene_variant
MELA-AU1113121401312140single base substitutionCTintron_variant
MELA-AU1113121461312146single base substitutionGAdownstream_gene_variant
MELA-AU1113121461312146single base substitutionGAexon_variant
MELA-AU1113121461312146single base substitutionGAintron_variant
MELA-AU1113126291312629single base substitutionGAdownstream_gene_variant
MELA-AU1113126291312629single base substitutionGAintron_variant
MELA-AU1113141621314162single base substitutionAGdownstream_gene_variant
MELA-AU1113141621314162single base substitutionAGintron_variant
MELA-AU1113141621314162single base substitutionAGupstream_gene_variant
MELA-AU1113144411314441single base substitutionGAdownstream_gene_variant
MELA-AU1113144411314441single base substitutionGAintron_variant
MELA-AU1113144411314441single base substitutionGAupstream_gene_variant
MELA-AU1113144781314478single base substitutionGAdownstream_gene_variant
MELA-AU1113144781314478single base substitutionGAintron_variant
MELA-AU1113144781314478single base substitutionGAupstream_gene_variant
MELA-AU1113145041314504single base substitutionGAdownstream_gene_variant
MELA-AU1113145041314504single base substitutionGAintron_variant
MELA-AU1113145041314504single base substitutionGAupstream_gene_variant
MELA-AU1113148411314841single base substitutionGAdownstream_gene_variant
MELA-AU1113148411314841single base substitutionGAintron_variant
MELA-AU1113148411314841single base substitutionGAupstream_gene_variant
MELA-AU1113151101315110single base substitutionCAdownstream_gene_variant
MELA-AU1113151101315110single base substitutionCAintron_variant
MELA-AU1113151101315110single base substitutionCAupstream_gene_variant
MELA-AU1113163551316355single base substitutionTCdownstream_gene_variant
MELA-AU1113163551316355single base substitutionTCintron_variant
MELA-AU1113163551316355single base substitutionTCupstream_gene_variant
MELA-AU1113164571316457single base substitutionCAdownstream_gene_variant
MELA-AU1113164571316457single base substitutionCAintron_variant
MELA-AU1113164571316457single base substitutionCAupstream_gene_variant
MELA-AU1113164791316479single base substitutionGAdownstream_gene_variant
MELA-AU1113164791316479single base substitutionGAintron_variant
MELA-AU1113164791316479single base substitutionGAupstream_gene_variant
MELA-AU1113165031316503single base substitutionGAdownstream_gene_variant
MELA-AU1113165031316503single base substitutionGAintron_variant
MELA-AU1113165031316503single base substitutionGAupstream_gene_variant
MELA-AU1113167871316787single base substitutionGAdownstream_gene_variant
MELA-AU1113167871316787single base substitutionGAexon_variant
MELA-AU1113167871316787single base substitutionGAintron_variant
MELA-AU1113167871316787single base substitutionGAupstream_gene_variant
MELA-AU1113168981316898single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
MELA-AU1113168981316898single base substitutionGAdownstream_gene_variant
MELA-AU1113168981316898single base substitutionGAexon_variant
MELA-AU1113168981316898single base substitutionGAintron_variant
MELA-AU1113168981316898single base substitutionGAstop_gainedR26*76C>T
MELA-AU1113168981316898single base substitutionGAstop_gainedR54*160C>T
MELA-AU1113168981316898single base substitutionGAupstream_gene_variant
MELA-AU1113171681317168single base substitutionCAdownstream_gene_variant
MELA-AU1113171681317168single base substitutionCAintron_variant
MELA-AU1113171681317168single base substitutionCAupstream_gene_variant
MELA-AU1113174991317499single base substitutionGAdownstream_gene_variant
MELA-AU1113174991317499single base substitutionGAintron_variant
MELA-AU1113174991317499single base substitutionGAupstream_gene_variant
MELA-AU1113177001317700single base substitutionGAdownstream_gene_variant
MELA-AU1113177001317700single base substitutionGAintron_variant
MELA-AU1113177001317700single base substitutionGAupstream_gene_variant
MELA-AU1113177521317752single base substitutionGAdownstream_gene_variant
MELA-AU1113177521317752single base substitutionGAintron_variant
MELA-AU1113177521317752single base substitutionGAupstream_gene_variant
MELA-AU1113187101318710single base substitutionGAdownstream_gene_variant
MELA-AU1113187101318710single base substitutionGAintron_variant
MELA-AU1113189151318915single base substitutionGAdownstream_gene_variant
MELA-AU1113189151318915single base substitutionGAintron_variant
MELA-AU1113189361318937multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU1113189361318937multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1113191071319107single base substitutionGAdownstream_gene_variant
MELA-AU1113191071319107single base substitutionGAintron_variant
MELA-AU1113195741319574single base substitutionGAexon_variant
MELA-AU1113195741319574single base substitutionGAintron_variant
MELA-AU1113198791319879single base substitutionGAintron_variant
MELA-AU1113201031320103single base substitutionGAintron_variant
MELA-AU1113203221320322single base substitutionATintron_variant
MELA-AU1113210041321004single base substitutionGAintron_variant
MELA-AU1113218641321864single base substitutionGAintron_variant
MELA-AU1113220811322081single base substitutionTGintron_variant
MELA-AU1113230511323051single base substitutionGAintron_variant
MELA-AU1113233341323334single base substitutionCTintron_variant
MELA-AU1113234411323441single base substitutionCTintron_variant
MELA-AU1113240781324078single base substitutionGAintron_variant
MELA-AU1113240781324078single base substitutionGAupstream_gene_variant
MELA-AU1113245651324565single base substitutionCTintron_variant
MELA-AU1113245651324565single base substitutionCTupstream_gene_variant
MELA-AU1113250851325085single base substitutionGAintron_variant
MELA-AU1113250851325085single base substitutionGAupstream_gene_variant
MELA-AU1113254721325472single base substitutionGAintron_variant
MELA-AU1113254721325472single base substitutionGAupstream_gene_variant
MELA-AU1113256601325660single base substitutionGAintron_variant
MELA-AU1113256601325660single base substitutionGAupstream_gene_variant
MELA-AU1113257191325719single base substitutionGCintron_variant
MELA-AU1113257191325719single base substitutionGCupstream_gene_variant
MELA-AU1113264681326468single base substitutionGAintron_variant
MELA-AU1113264681326468single base substitutionGAupstream_gene_variant
MELA-AU1113266571326657single base substitutionAGintron_variant
MELA-AU1113266571326657single base substitutionAGupstream_gene_variant
MELA-AU1113269451326945single base substitutionGAintron_variant
MELA-AU1113269451326945single base substitutionGAupstream_gene_variant
MELA-AU1113269521326952single base substitutionGAintron_variant
MELA-AU1113269521326952single base substitutionGAupstream_gene_variant
MELA-AU1113276041327604single base substitutionGAintron_variant
MELA-AU1113276041327604single base substitutionGAupstream_gene_variant
MELA-AU1113278861327886single base substitutionTGintron_variant
MELA-AU1113278861327886single base substitutionTGupstream_gene_variant
MELA-AU1113286261328626single base substitutionCTintron_variant
MELA-AU1113286261328626single base substitutionCTupstream_gene_variant
MELA-AU1113286421328642single base substitutionGAintron_variant
MELA-AU1113286421328642single base substitutionGAupstream_gene_variant
MELA-AU1113288231328823single base substitutionCTintron_variant
MELA-AU1113288231328823single base substitutionCTupstream_gene_variant
MELA-AU1113299271329927single base substitutionTAintron_variant
MELA-AU1113299271329927single base substitutionTAupstream_gene_variant
MELA-AU1113303041330304single base substitutionGAintron_variant
MELA-AU1113303041330304single base substitutionGAupstream_gene_variant
MELA-AU1113306971330697single base substitutionGAintron_variant
MELA-AU1113306971330697single base substitutionGAmissense_variantP11L32C>T
MELA-AU1113306971330697single base substitutionGAsplice_region_variant
MELA-AU1113306971330697single base substitutionGAupstream_gene_variant
MELA-AU1113308741330874single base substitutionCT5_prime_UTR_variant
MELA-AU1113308741330874single base substitutionCTexon_variant
MELA-AU1113308741330874single base substitutionCTupstream_gene_variant
MELA-AU1113309081330908single base substitutionGAupstream_gene_variant
MELA-AU1113309171330917single base substitutionCTupstream_gene_variant
MELA-AU1113309171330918multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU1113309181330918single base substitutionCTupstream_gene_variant
MELA-AU1113309191330919insertion of <=200bp-Tupstream_gene_variant
MELA-AU1113309211330921single base substitutionCTupstream_gene_variant
MELA-AU1113323771332377single base substitutionGAupstream_gene_variant
MELA-AU1113324391332439single base substitutionCTupstream_gene_variant
MELA-AU1113329931332993single base substitutionGAupstream_gene_variant
MELA-AU1113332381333238single base substitutionGAupstream_gene_variant
MELA-AU1113336411333641single base substitutionGAupstream_gene_variant
MELA-AU1113338971333897single base substitutionTAupstream_gene_variant
MELA-AU1113344341334434single base substitutionCTupstream_gene_variant
MELA-AU1113347011334701single base substitutionCTupstream_gene_variant
MELA-AU1113348111334811single base substitutionCTupstream_gene_variant
MELA-AU1113353961335396single base substitutionCTupstream_gene_variant
MELA-AU1113355661335566single base substitutionCTupstream_gene_variant
MELA-AU1113357751335775single base substitutionCTupstream_gene_variant
ORCA-IN1113275121327512single base substitutionCGintron_variant
ORCA-IN1113275121327512single base substitutionCGupstream_gene_variant
OV-AU1112942581294258single base substitutionCAdownstream_gene_variant
OV-AU1112960921296092single base substitutionGA3_prime_UTR_variant
OV-AU1112960921296092single base substitutionGAdownstream_gene_variant
OV-AU1112998651299865single base substitutionCAintron_variant
OV-AU1113029071302907single base substitutionGCintron_variant
OV-AU1113057691305769single base substitutionCTdownstream_gene_variant
OV-AU1113057691305769single base substitutionCTintron_variant
OV-AU1113073491307349single base substitutionGTdownstream_gene_variant
OV-AU1113073491307349single base substitutionGTintron_variant
OV-AU1113104641310464single base substitutionCAdownstream_gene_variant
OV-AU1113104641310464single base substitutionCAintron_variant
OV-AU1113128101312810single base substitutionGAdownstream_gene_variant
OV-AU1113128101312810single base substitutionGAintron_variant
OV-AU1113132201313220single base substitutionCTdownstream_gene_variant
OV-AU1113132201313220single base substitutionCTexon_variant
OV-AU1113132201313220single base substitutionCTintron_variant
OV-AU1113235621323562single base substitutionTAintron_variant
OV-AU1113243191324319single base substitutionAGintron_variant
OV-AU1113243191324319single base substitutionAGupstream_gene_variant
OV-AU1113253891325389single base substitutionGAintron_variant
OV-AU1113253891325389single base substitutionGAupstream_gene_variant
OV-AU1113272841327284single base substitutionCAexon_variant
OV-AU1113272841327284single base substitutionCAintron_variant
OV-AU1113272841327284single base substitutionCAupstream_gene_variant
OV-AU1113276751327675single base substitutionGAintron_variant
OV-AU1113276751327675single base substitutionGAupstream_gene_variant
PACA-AU1112910011291001single base substitutionCTdownstream_gene_variant
PACA-AU1112947321294732single base substitutionATdownstream_gene_variant
PACA-AU1113004221300422single base substitutionCTintron_variant
PACA-AU1113011641301164single base substitutionATintron_variant
PACA-AU1113013171301317single base substitutionGAintron_variant
PACA-AU1113028021302802single base substitutionGAintron_variant
PACA-AU1113036401303640single base substitutionCTintron_variant
PACA-AU1113077611307761single base substitutionCTdownstream_gene_variant
PACA-AU1113077611307761single base substitutionCTintron_variant
PACA-AU1113082301308230single base substitutionCTdownstream_gene_variant
PACA-AU1113082301308230single base substitutionCTintron_variant
PACA-AU1113106161310616single base substitutionCTdownstream_gene_variant
PACA-AU1113106161310616single base substitutionCTintron_variant
PACA-AU1113115741311574single base substitutionGAdownstream_gene_variant
PACA-AU1113115741311574single base substitutionGAexon_variant
PACA-AU1113115741311574single base substitutionGAintron_variant
PACA-AU1113115741311574single base substitutionGAsynonymous_variantY14Y42C>T
PACA-AU1113115741311574single base substitutionGAsynonymous_variantY33Y99C>T
PACA-AU1113115741311574single base substitutionGAsynonymous_variantY55Y165C>T
PACA-AU1113115741311574single base substitutionGAsynonymous_variantY83Y249C>T
PACA-AU1113137921313792single base substitutionCAdownstream_gene_variant
PACA-AU1113137921313792single base substitutionCAintron_variant
PACA-AU1113137921313792single base substitutionCAupstream_gene_variant
PACA-AU1113168751316875single base substitutionCTdownstream_gene_variant
PACA-AU1113168751316875single base substitutionCTexon_variant
PACA-AU1113168751316875single base substitutionCTintron_variant
PACA-AU1113168751316875single base substitutionCTsplice_region_variant
PACA-AU1113168751316875single base substitutionCTupstream_gene_variant
PACA-AU1113208421320842single base substitutionTCintron_variant
PACA-AU1113227001322700single base substitutionAGintron_variant
PACA-AU1113234191323419single base substitutionGAintron_variant
PACA-AU1113277111327711single base substitutionCTintron_variant
PACA-AU1113277111327711single base substitutionCTupstream_gene_variant
PACA-AU1113292431329243single base substitutionCTintron_variant
PACA-AU1113292431329243single base substitutionCTupstream_gene_variant
PACA-AU1113340841334084single base substitutionAGupstream_gene_variant
PACA-AU1113341231334123single base substitutionGAupstream_gene_variant
PACA-CA1112915631291563single base substitutionGAdownstream_gene_variant
PACA-CA1112928491292849single base substitutionCTdownstream_gene_variant
PACA-CA1112948381294853deletion of <=200bpCCGGCGATGGGGACGC-downstream_gene_variant
PACA-CA1112952551295255single base substitutionCTdownstream_gene_variant
PACA-CA1112957501295750single base substitutionCA3_prime_UTR_variant
PACA-CA1112957501295750single base substitutionCAdownstream_gene_variant
PACA-CA1112968041296804single base substitutionGA3_prime_UTR_variant
PACA-CA1112968041296804single base substitutionGAdownstream_gene_variant
PACA-CA1112974911297491single base substitutionGA3_prime_UTR_variant
PACA-CA1112974911297491single base substitutionGAdownstream_gene_variant
PACA-CA1113000001300000single base substitutionTCintron_variant
PACA-CA1113010121301012single base substitutionGAintron_variant
PACA-CA1113021721302172single base substitutionCTintron_variant
PACA-CA1113076231307623single base substitutionCTdownstream_gene_variant
PACA-CA1113076231307623single base substitutionCTintron_variant
PACA-CA1113094211309421single base substitutionGTdownstream_gene_variant
PACA-CA1113094211309421single base substitutionGTintron_variant
PACA-CA1113142531314253single base substitutionCTdownstream_gene_variant
PACA-CA1113142531314253single base substitutionCTintron_variant
PACA-CA1113142531314253single base substitutionCTupstream_gene_variant
PACA-CA1113186721318672single base substitutionCTdownstream_gene_variant
PACA-CA1113186721318672single base substitutionCTintron_variant
PACA-CA1113206041320604single base substitutionGCintron_variant
PACA-CA1113215961321596single base substitutionGAintron_variant
PACA-CA1113242171324217single base substitutionACintron_variant
PACA-CA1113242171324217single base substitutionACupstream_gene_variant
PACA-CA1113306721330672single base substitutionCTintron_variant
PACA-CA1113306721330672single base substitutionCTupstream_gene_variant
PACA-CA1113337291333729single base substitutionAGupstream_gene_variant
PAEN-AU1113323761332376single base substitutionGAupstream_gene_variant
PAEN-IT1113138811313881single base substitutionGAdownstream_gene_variant
PAEN-IT1113138811313881single base substitutionGAintron_variant
PAEN-IT1113138811313881single base substitutionGAupstream_gene_variant
PAEN-IT1113155591315559single base substitutionCTdownstream_gene_variant
PAEN-IT1113155591315559single base substitutionCTintron_variant
PAEN-IT1113155591315559single base substitutionCTupstream_gene_variant
PAEN-IT1113302031330203single base substitutionGAintron_variant
PAEN-IT1113302031330203single base substitutionGAupstream_gene_variant
PBCA-DE1112946431294643single base substitutionGAdownstream_gene_variant
PBCA-DE1112954371295437single base substitutionGAdownstream_gene_variant
PBCA-DE1112970921297092single base substitutionGA3_prime_UTR_variant
PBCA-DE1112970921297092single base substitutionGAdownstream_gene_variant
PBCA-DE1113022021302202single base substitutionCTintron_variant
PBCA-DE1113061401306140single base substitutionGAdownstream_gene_variant
PBCA-DE1113061401306140single base substitutionGAintron_variant
PBCA-DE1113109771310977single base substitutionCTdownstream_gene_variant
PBCA-DE1113109771310977single base substitutionCTintron_variant
PBCA-DE1113214801321480single base substitutionTCintron_variant
PRAD-CA1112964671296467single base substitutionCT3_prime_UTR_variant
PRAD-CA1112964671296467single base substitutionCTdownstream_gene_variant
PRAD-UK1112986031298603single base substitutionGAintron_variant
PRAD-UK1113296501329650single base substitutionCAintron_variant
PRAD-UK1113296501329650single base substitutionCAupstream_gene_variant
RECA-EU1112987901298790single base substitutionGAintron_variant
RECA-EU1112997921299792single base substitutionGAintron_variant
RECA-EU1113152151315215single base substitutionCTdownstream_gene_variant
RECA-EU1113152151315215single base substitutionCTintron_variant
RECA-EU1113152151315215single base substitutionCTupstream_gene_variant
RECA-EU1113201941320194single base substitutionCTintron_variant
RECA-EU1113204461320446single base substitutionTCintron_variant
RECA-EU1113207341320734single base substitutionACintron_variant
RECA-EU1113316171331617single base substitutionACupstream_gene_variant
SKCA-BR1112928021292802single base substitutionGAdownstream_gene_variant
SKCA-BR1112936071293607single base substitutionGCdownstream_gene_variant
SKCA-BR1112947661294766single base substitutionAGdownstream_gene_variant
SKCA-BR1112955921295592single base substitutionCGdownstream_gene_variant
SKCA-BR1112961031296103single base substitutionAG3_prime_UTR_variant
SKCA-BR1112961031296103single base substitutionAGdownstream_gene_variant
SKCA-BR1112980581298058single base substitutionTG3_prime_UTR_variant
SKCA-BR1112980581298058single base substitutionTGdownstream_gene_variant
SKCA-BR1112999421299942single base substitutionGAintron_variant
SKCA-BR1113057021305702single base substitutionCTdownstream_gene_variant
SKCA-BR1113057021305702single base substitutionCTintron_variant
SKCA-BR1113077871307787single base substitutionGAdownstream_gene_variant
SKCA-BR1113077871307787single base substitutionGAintron_variant
SKCA-BR1113116231311623single base substitutionTC5_prime_UTR_variant
SKCA-BR1113116231311623single base substitutionTCdownstream_gene_variant
SKCA-BR1113116231311623single base substitutionTCexon_variant
SKCA-BR1113116231311623single base substitutionTCintron_variant
SKCA-BR1113116231311623single base substitutionTCmissense_variantN17S50A>G
SKCA-BR1113116231311623single base substitutionTCmissense_variantN39S116A>G
SKCA-BR1113116231311623single base substitutionTCmissense_variantN67S200A>G
SKCA-BR1113154881315488single base substitutionAGdownstream_gene_variant
SKCA-BR1113154881315488single base substitutionAGintron_variant
SKCA-BR1113154881315488single base substitutionAGupstream_gene_variant
SKCA-BR1113156731315673single base substitutionAGdownstream_gene_variant
SKCA-BR1113156731315673single base substitutionAGintron_variant
SKCA-BR1113156731315673single base substitutionAGupstream_gene_variant
SKCA-BR1113162721316272single base substitutionTCdownstream_gene_variant
SKCA-BR1113162721316272single base substitutionTCintron_variant
SKCA-BR1113162721316272single base substitutionTCupstream_gene_variant
SKCA-BR1113171151317115single base substitutionGCdownstream_gene_variant
SKCA-BR1113171151317115single base substitutionGCintron_variant
SKCA-BR1113171151317115single base substitutionGCupstream_gene_variant
SKCA-BR1113171211317121single base substitutionACdownstream_gene_variant
SKCA-BR1113171211317121single base substitutionACintron_variant
SKCA-BR1113171211317121single base substitutionACupstream_gene_variant
SKCA-BR1113178011317801single base substitutionATdownstream_gene_variant
SKCA-BR1113178011317801single base substitutionATintron_variant
SKCA-BR1113178011317801single base substitutionATupstream_gene_variant
SKCA-BR1113211711321171single base substitutionTGintron_variant
SKCA-BR1113243641324364single base substitutionGAintron_variant
SKCA-BR1113243641324364single base substitutionGAupstream_gene_variant
SKCA-BR1113273311327331single base substitutionTCexon_variant
SKCA-BR1113273311327331single base substitutionTCintron_variant
SKCA-BR1113273311327331single base substitutionTCupstream_gene_variant
SKCA-BR1113275001327500single base substitutionCTintron_variant
SKCA-BR1113275001327500single base substitutionCTupstream_gene_variant
SKCA-BR1113286161328616single base substitutionTCintron_variant
SKCA-BR1113286161328616single base substitutionTCupstream_gene_variant
SKCA-BR1113300641330064insertion of <=200bp-CCCGCCTCCACCTGTGGGGCCATAAGGGTGCCGGGAintron_variant
SKCA-BR1113300641330064insertion of <=200bp-CCCGCCTCCACCTGTGGGGCCATAAGGGTGCCGGGAupstream_gene_variant
SKCA-BR1113300741330074insertion of <=200bp-CCTGTGGGGCCATAAGGGTGCCGGGACCGCCTCCACintron_variant
SKCA-BR1113300741330074insertion of <=200bp-CCTGTGGGGCCATAAGGGTGCCGGGACCGCCTCCACupstream_gene_variant
SKCA-BR1113300781330078single base substitutionGTintron_variant
SKCA-BR1113300781330078single base substitutionGTupstream_gene_variant
SKCA-BR1113300871330087single base substitutionCAintron_variant
SKCA-BR1113300871330087single base substitutionCAupstream_gene_variant
SKCA-BR1113300951330095single base substitutionGCintron_variant
SKCA-BR1113300951330095single base substitutionGCupstream_gene_variant
SKCA-BR1113300981330098single base substitutionAGintron_variant
SKCA-BR1113300981330098single base substitutionAGupstream_gene_variant
SKCA-BR1113300991330099single base substitutionCAintron_variant
SKCA-BR1113300991330099single base substitutionCAupstream_gene_variant
SKCA-BR1113301111330112deletion of <=200bpTG-intron_variant
SKCA-BR1113301111330112deletion of <=200bpTG-upstream_gene_variant
SKCA-BR1113301341330134single base substitutionGAintron_variant
SKCA-BR1113301341330134single base substitutionGAupstream_gene_variant
SKCA-BR1113309171330917single base substitutionCTupstream_gene_variant
SKCA-BR1113309251330925single base substitutionCTupstream_gene_variant
SKCM-US1113115301311530single base substitutionGAdownstream_gene_variant
SKCM-US1113115301311530single base substitutionGAexon_variant
SKCM-US1113115301311530single base substitutionGAintron_variant
SKCM-US1113115301311530single base substitutionGAmissense_variantP29L86C>T
SKCM-US1113115301311530single base substitutionGAmissense_variantP48L143C>T
SKCM-US1113115301311530single base substitutionGAmissense_variantP70L209C>T
SKCM-US1113115301311530single base substitutionGAmissense_variantP98L293C>T
STAD-US1112983401298340single base substitutionCT3_prime_UTR_variant
STAD-US1112983401298340single base substitutionCTdownstream_gene_variant
STAD-US1112983401298340single base substitutionCTmissense_variantV183M547G>A
STAD-US1112983401298340single base substitutionCTmissense_variantV191M571G>A
STAD-US1112983401298340single base substitutionCTmissense_variantV202M604G>A
STAD-US1112983401298340single base substitutionCTmissense_variantV224M670G>A
STAD-US1112983401298340single base substitutionCTmissense_variantV252M754G>A
STAD-US1113115031311503single base substitutionGAdownstream_gene_variant
STAD-US1113115031311503single base substitutionGAexon_variant
STAD-US1113115031311503single base substitutionGAintron_variant
STAD-US1113115031311503single base substitutionGAmissense_variantT107M320C>T
STAD-US1113115031311503single base substitutionGAmissense_variantT38M113C>T
STAD-US1113115031311503single base substitutionGAmissense_variantT57M170C>T
STAD-US1113115031311503single base substitutionGAmissense_variantT79M236C>T
STAD-US1113115721311572single base substitutionGAdownstream_gene_variant
STAD-US1113115721311572single base substitutionGAexon_variant
STAD-US1113115721311572single base substitutionGAintron_variant
STAD-US1113115721311572single base substitutionGAmissense_variantA15V44C>T
STAD-US1113115721311572single base substitutionGAmissense_variantA34V101C>T
STAD-US1113115721311572single base substitutionGAmissense_variantA56V167C>T
STAD-US1113115721311572single base substitutionGAmissense_variantA84V251C>T
STAD-US1113115851311585single base substitutionGAdownstream_gene_variant
STAD-US1113115851311585single base substitutionGAexon_variant
STAD-US1113115851311585single base substitutionGAintron_variant
STAD-US1113115851311585single base substitutionGAmissense_variantR11C31C>T
STAD-US1113115851311585single base substitutionGAmissense_variantR30C88C>T
STAD-US1113115851311585single base substitutionGAmissense_variantR52C154C>T
STAD-US1113115851311585single base substitutionGAmissense_variantR80C238C>T
STAD-US1113115911311591single base substitutionGAdownstream_gene_variant
STAD-US1113115911311591single base substitutionGAexon_variant
STAD-US1113115911311591single base substitutionGAintron_variant
STAD-US1113115911311591single base substitutionGAstop_gainedR28*82C>T
STAD-US1113115911311591single base substitutionGAstop_gainedR50*148C>T
STAD-US1113115911311591single base substitutionGAstop_gainedR78*232C>T
STAD-US1113115911311591single base substitutionGAstop_gainedR9*25C>T
THCA-SA1112966491296649single base substitutionGA3_prime_UTR_variant
THCA-SA1112966491296649single base substitutionGAdownstream_gene_variant
THCA-SA1112973351297335single base substitutionCT3_prime_UTR_variant
THCA-SA1112973351297335single base substitutionCTdownstream_gene_variant
UCEC-US1113098931309893single base substitutionGAdownstream_gene_variant
UCEC-US1113098931309893single base substitutionGAexon_variant
UCEC-US1113098931309893single base substitutionGAintron_variant
UCEC-US1113098931309893single base substitutionGAsynonymous_variantD110D330C>T
UCEC-US1113098931309893single base substitutionGAsynonymous_variantD132D396C>T
UCEC-US1113098931309893single base substitutionGAsynonymous_variantD160D480C>T
UCEC-US1113098931309893single base substitutionGAsynonymous_variantD91D273C>T
UCEC-US1113098931309893single base substitutionGAsynonymous_variantD99D297C>T
UCEC-US1113114821311482single base substitutionGTdownstream_gene_variant
UCEC-US1113114821311482single base substitutionGTexon_variant
UCEC-US1113114821311482single base substitutionGTintron_variant
UCEC-US1113114821311482single base substitutionGTmissense_variantS114Y341C>A
UCEC-US1113114821311482single base substitutionGTmissense_variantS45Y134C>A
UCEC-US1113114821311482single base substitutionGTmissense_variantS64Y191C>A
UCEC-US1113114821311482single base substitutionGTmissense_variantS86Y257C>A
UCEC-US1113115141311514single base substitutionGTdownstream_gene_variant
UCEC-US1113115141311514single base substitutionGTexon_variant
UCEC-US1113115141311514single base substitutionGTintron_variant
UCEC-US1113115141311514single base substitutionGTsynonymous_variantV103V309C>A
UCEC-US1113115141311514single base substitutionGTsynonymous_variantV34V102C>A
UCEC-US1113115141311514single base substitutionGTsynonymous_variantV53V159C>A
UCEC-US1113115141311514single base substitutionGTsynonymous_variantV75V225C>A
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-BR-7958-01COSM4019404c.232C>Tp.R78*Substitution - Nonsense11:1290361-1290361-
HCC107COSM1604309c.778A>Gp.K260ESubstitution - Missense11:1277086-1277086-
TCGA-EE-A29E-06COSM3445397c.293C>Tp.P98LSubstitution - Missense11:1290300-1290300-
067TCOSM1730393c.521T>Ap.L174QSubstitution - Missense11:1286091-1286091-
BD6TCOSM5499081c.611G>Tp.G204VSubstitution - Missense11:1277253-1277253-
CCK81COSM2089623c.283G>Ap.A95TSubstitution - Missense11:1290310-1290310-
CHC892TCOSM4796530c.117G>Ap.A39ASubstitution - coding silent11:1295711-1295711-
S00827COSM316071c.270G>Tp.T90TSubstitution - coding silent11:1290323-1290323-
05-P8014COSM4574172c.713A>Gp.Q238RSubstitution - Missense11:1277151-1277151-
BCM723TCOSM4956304c.518C>Tp.A173VSubstitution - Missense11:1288625-1288625-
TCGA-D1-A103-01COSM925038c.309C>Ap.V103VSubstitution - coding silent11:1290284-1290284-
RKOCOSM4647284c.52C>Ap.P18TSubstitution - Missense11:1295776-1295776-
HCC107TCOSM1604309c.778A>Gp.K260ESubstitution - Missense11:1277086-1277086-
4_RESISTANTCOSM1724355c.343T>Cp.F115LSubstitution - Missense11:1290250-1290250-
61COSM5739126c.331G>Tp.G111CSubstitution - Missense11:1290262-1290262-
TCGA-AD-6964-01COSM1352469c.74C>Tp.T25MSubstitution - Missense11:1295754-1295754-
TCGA-A5-A0VP-01COSM925036c.480C>Tp.D160DSubstitution - coding silent11:1288663-1288663-
7313COSM5613321c.556G>Ap.V186MSubstitution - Missense11:1286056-1286056-
8067242COSM3769246c.183G>Ap.Q61QSubstitution - coding silent11:1295645-1295645-
TCGA-BR-4361-01COSM4019330c.754G>Ap.V252MSubstitution - Missense11:1277110-1277110-
TCGA-BR-8487-01COSM4019402c.320C>Tp.T107MSubstitution - Missense11:1290273-1290273-
TCGA-CM-4746-01COSM1352412c.714G>Tp.Q238HSubstitution - Missense11:1277150-1277150-
VACO10COSM4656824c.253G>Ap.V85MSubstitution - Missense11:1290340-1290340-
61COSM5739125c.673G>Ap.A225TSubstitution - Missense11:1277191-1277191-
M010COSM1739743c.251C>Tp.A84VSubstitution - Missense11:1290342-1290342-
TCGA-AP-A0LM-01COSM925037c.341C>Ap.S114YSubstitution - Missense11:1290252-1290252-
TCGA-AA-3492-01COSM1352467c.325C>Tp.P109SSubstitution - Missense11:1290268-1290268-
8012854COSM3383330c.249C>Tp.Y83YSubstitution - coding silent11:1290344-1290344-
ESOSCC155TCOSM1171763c.592G>Ap.G198SSubstitution - Missense11:1286020-1286020-
TCGA-CK-4947-01COSM1352468c.109G>Ap.A37TSubstitution - Missense11:1295719-1295719-
PTC-7CCOSM428715c.417G>Ap.P139PSubstitution - coding silent11:1288726-1288726-
TCGA-BR-8363-01COSM1739743c.251C>Tp.A84VSubstitution - Missense11:1290342-1290342-
CSB21COSM5027338c.361G>Tp.D121YSubstitution - Missense11:1290232-1290232-
HN_62426COSM122103c.270G>Ap.T90TSubstitution - coding silent11:1290323-1290323-
TCGA-18-3406-01COSM687237c.205G>Ap.G69SSubstitution - Missense11:1290388-1290388-
CRC-06TCOSM5456097c.233G>Ap.R78QSubstitution - Missense11:1290360-1290360-
TCGA-DK-A2I4-01COSM3791331c.770G>Ap.R257QSubstitution - Missense11:1277094-1277094-
T24COSM5341443c.269C>Tp.T90MSubstitution - Missense11:1290324-1290324-
ESCC-D8COSM5046521c.619G>Ap.A207TSubstitution - Missense11:1277245-1277245-
587234COSM1230059c.280G>Tp.G94CSubstitution - Missense11:1290313-1290313-
RK119_C01COSM3738957c.576G>Ap.V192VSubstitution - coding silent11:1286036-1286036-
YULONECOSM5372045c.681C>Tp.P227PSubstitution - coding silent11:1277183-1277183-
PA285COSM1162938c.263C>Tp.T88MSubstitution - Missense11:1290330-1290330-
TCGA-FG-A4MU-01COSM3967416c.646G>Ap.V216MSubstitution - Missense11:1277218-1277218-
4_PRE-TREATMENTCOSM1724355c.343T>Cp.F115LSubstitution - Missense11:1290250-1290250-
CHC892TCOSM4796530c.117G>Ap.A39ASubstitution - coding silent11:1295711-1295711-
T3152COSM4735265c.672C>Tp.N224NSubstitution - coding silent11:1277192-1277192-
CSCC-38-TCOSM4509143c.798C>Tp.S266SSubstitution - coding silent11:1277066-1277066-
40MCOSM5586828c.579C>Tp.Y193YSubstitution - coding silent11:1286033-1286033-
8068539COSM3383330c.249C>Tp.Y83YSubstitution - coding silent11:1290344-1290344-
ESO-250COSM1268297c.683G>Ap.R228HSubstitution - Missense11:1277181-1277181-
TCGA-BR-8680-01COSM4019403c.238C>Tp.R80CSubstitution - Missense11:1290355-1290355-
S00827COSM316071c.270G>Tp.T90TSubstitution - coding silent11:1290323-1290323-
T35COSM5341442c.334G>Ap.V112MSubstitution - Missense11:1290259-1290259-
LUAD-CHTN-MAD06-00668COSM358476c.215G>Ap.R72HSubstitution - Missense11:1290378-1290378-
BCM723TCOSM4956304c.518C>Tp.A173VSubstitution - Missense11:1288625-1288625-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.36852711p15.56062772460876|CGAP|BC004420|A/G|coding|Pro139Pro|540|Validated;
2460876|CGAP|BC012057|A/G|coding|Pro139Pro|505|Validated;
2460876|CGAP|BC018272|A/G|coding|Pro139Pro|497|Validated
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
CAMissensep.D121Yc.361G>T111311462BRCA
CASynonymousp.T90Tc.270G>T111311553SCLC
CTMissensep.G69Sc.205G>A111311618LUSC
CTMissensep.R257Qc.770G>A111298324ALL
CTMissensep.R257Qc.770G>A111298324BLCA
CTMissensep.V186Mc.556G>A111307286NSCLC
CTSynonymousp.T90Tc.270G>A111311553HNSC
GA3-UTRSNV.c.822+1180C>T111297092MB
GAMissensep.S266Fc.797C>T111298297CM
GASynonymousp.D160Dc.480C>T111309893UCEC
GASynonymousp.V169Vc.507C>T111309866HNSC
GTMissensep.Q256Kc.766C>A111298328LUAD
TA3-UTRSNV.c.822+622A>T111297650HC
TCSynonymousp.V60Vc.180A>G111316878LUAD