Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 23 15262642 15262642 + Missense_Mutation SNP G G A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chrX:15262642G>A c.871C>T c.(871-873)Ctc>Ttc p.L291F BLCA 23 15266882 15266882 + Silent SNP G G C TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chrX:15266882G>C c.744C>G c.(742-744)ctC>ctG p.L248L BRCA 23 15262744 15262744 + Missense_Mutation SNP A A G TCGA-E9-A22E-01A-11D-A159-09 TCGA-E9-A22E-10A-01D-A159-09 g.chrX:15262744A>G c.769T>C c.(769-771)Tct>Cct p.S257P BRCA 23 15267033 15267033 + Missense_Mutation SNP C C T TCGA-A2-A04P-01A-31D-A128-09 TCGA-A2-A04P-10A-01W-A055-09 g.chrX:15267033C>T c.593G>A c.(592-594)gGt>gAt p.G198D BRCA 23 15270445 15270445 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:15270445G>T c.364C>A c.(364-366)Ctg>Atg p.L122M BRCA 23 15272920 15272920 + Missense_Mutation SNP T T C TCGA-A8-A06Z-01A-11W-A019-09 TCGA-A8-A06Z-10A-01W-A021-09 g.chrX:15272920T>C c.221A>G c.(220-222)cAt>cGt p.H74R CESC 23 15266972 15266972 + Silent SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chrX:15266972G>C c.654C>G c.(652-654)ctC>ctG p.L218L COAD 23 15268633 15268633 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:15268633T>C c.487A>G c.(487-489)Aag>Gag p.K163E COAD 23 15272944 15272944 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:15272944G>A c.197C>T c.(196-198)aCg>aTg p.T66M COAD 23 15287935 15287935 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:15287935C>T c.62G>A c.(61-63)gGc>gAc p.G21D COADREAD 23 15268633 15268633 + Missense_Mutation SNP T T C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:15268633T>C c.487A>G c.(487-489)Aag>Gag p.K163E COADREAD 23 15272944 15272944 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:15272944G>A c.197C>T c.(196-198)aCg>aTg p.T66M COADREAD 23 15287935 15287935 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:15287935C>T c.62G>A c.(61-63)gGc>gAc p.G21D ESCA 23 15287931 15287931 + Silent SNP G G A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chrX:15287931G>A c.66C>T c.(64-66)atC>atT p.I22I GBM 23 15266989 15266989 + Nonsense_Mutation SNP C C A TCGA-76-4931-01A-01D-1486-08 TCGA-76-4931-10A-01D-1486-08 g.chrX:15266989C>A c.637G>T c.(637-639)Gag>Tag p.E213* GBMLGG 23 15266936 15266936 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:15266936A>G c.690T>C c.(688-690)gcT>gcC p.A230A GBMLGG 23 15266989 15266989 + Nonsense_Mutation SNP C C A TCGA-76-4931-01A-01D-1486-08 TCGA-76-4931-10A-01D-1486-08 g.chrX:15266989C>A c.637G>T c.(637-639)Gag>Tag p.E213* GBMLGG 23 15268608 15268608 + Missense_Mutation SNP A A T TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chrX:15268608A>T c.512T>A c.(511-513)cTc>cAc p.L171H GBMLGG 23 15272893 15272893 + Missense_Mutation SNP G G A TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chrX:15272893G>A c.248C>T c.(247-249)tCt>tTt p.S83F GBMLGG 23 15287957 15287957 + Missense_Mutation SNP C C T TCGA-FG-A87Q-01A-11D-A36O-08 TCGA-FG-A87Q-10A-01D-A367-08 g.chrX:15287957C>T c.40G>A c.(40-42)Gcg>Acg p.A14T HNSC 23 15262664 15262664 + Silent SNP G G A TCGA-BA-A6DF-01A-11D-A30E-08 TCGA-BA-A6DF-10A-01D-A30H-08 g.chrX:15262664G>A c.849C>T c.(847-849)ctC>ctT p.L283L HNSC 23 15266983 15266983 + Missense_Mutation SNP C C A TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chrX:15266983C>A c.643G>T c.(643-645)Gcc>Tcc p.A215S HNSC 23 15268558 15268558 + Nonsense_Mutation SNP C C A TCGA-BA-5149-01A-01D-1512-08 TCGA-BA-5149-10A-01D-1512-08 g.chrX:15268558C>A c.562G>T c.(562-564)Gag>Tag p.E188* HNSC 23 15270437 15270437 + Silent SNP G G A TCGA-CV-7437-01A-21D-2129-08 TCGA-CV-7437-10A-01D-2129-08 g.chrX:15270437G>A c.372C>T c.(370-372)caC>caT p.H124H LGG 23 15266936 15266936 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:15266936A>G c.690T>C c.(688-690)gcT>gcC p.A230A LGG 23 15268608 15268608 + Missense_Mutation SNP A A T TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chrX:15268608A>T c.512T>A c.(511-513)cTc>cAc p.L171H LGG 23 15272893 15272893 + Missense_Mutation SNP G G A TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chrX:15272893G>A c.248C>T c.(247-249)tCt>tTt p.S83F LGG 23 15287957 15287957 + Missense_Mutation SNP C C T TCGA-FG-A87Q-01A-11D-A36O-08 TCGA-FG-A87Q-10A-01D-A367-08 g.chrX:15287957C>T c.40G>A c.(40-42)Gcg>Acg p.A14T LUAD 23 15266879 15266879 + Silent SNP G G A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chrX:15266879G>A c.747C>T c.(745-747)ttC>ttT p.F249F LUAD 23 15266947 15266947 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chrX:15266947C>A c.679G>T c.(679-681)Gcc>Tcc p.A227S LUAD 23 15267024 15267024 + Missense_Mutation SNP G G T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:15267024G>T c.602C>A c.(601-603)tCc>tAc p.S201Y LUAD 23 15268584 15268584 + Missense_Mutation SNP T T C TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chrX:15268584T>C c.536A>G c.(535-537)cAg>cGg p.Q179R LUAD 23 15276996 15276996 + Missense_Mutation SNP T T A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:15276996T>A c.166A>T c.(166-168)Atc>Ttc p.I56F LUAD 23 15287910 15287910 + Silent SNP C C T TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chrX:15287910C>T c.87G>A c.(85-87)ttG>ttA p.L29L LUAD 23 15287938 15287938 + Missense_Mutation SNP G G T TCGA-97-7546-01A-11D-2036-08 TCGA-97-7546-10A-01D-2036-08 g.chrX:15287938G>T c.59C>A c.(58-60)cCt>cAt p.P20H LUSC 23 15268561 15268561 + Missense_Mutation SNP G G C TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chrX:15268561G>C c.559C>G c.(559-561)Ctg>Gtg p.L187V LUSC 23 15268612 15268612 + Missense_Mutation SNP G G T TCGA-21-1070-01A-01D-1521-08 TCGA-21-1070-11A-01D-1521-08 g.chrX:15268612G>T c.508C>A c.(508-510)Cca>Aca p.P170T LUSC 23 15270382 15270382 + Missense_Mutation SNP T T A TCGA-22-5492-01A-01D-1632-08 TCGA-22-5492-11A-01D-1632-08 g.chrX:15270382T>A c.427A>T c.(427-429)Agg>Tgg p.R143W LUSC 23 15287980 15287981 + Missense_Mutation DNP CC CC AG TCGA-56-6545-01A-11D-1817-08 TCGA-56-6545-10A-01D-1817-08 g.chrX:15287980_15287981CC>AG c.16_17GG>CT c.(16-18)GGg>CTg p.G6L PAAD 23 15266898 15266898 + Missense_Mutation SNP C C T TCGA-IB-7652-01A-11D-2154-08 TCGA-IB-7652-10A-01D-2154-08 g.chrX:15266898C>T c.728G>A c.(727-729)aGc>aAc p.S243N PAAD 23 15266926 15266926 + Missense_Mutation SNP G G A TCGA-IB-7652-01A-11D-2154-08 TCGA-IB-7652-10A-01D-2154-08 g.chrX:15266926G>A c.700C>T c.(700-702)Cgt>Tgt p.R234C PAAD 23 15276992 15276992 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:15276992C>A c.170G>T c.(169-171)aGc>aTc p.S57I PCPG 23 15267054 15267054 + Missense_Mutation SNP G G A TCGA-S7-A7WT-01A-12D-A35I-08 TCGA-S7-A7WT-10A-01D-A35G-08 g.chrX:15267054G>A c.572C>T c.(571-573)gCg>gTg p.A191V PRAD 23 15270503 15270503 + Nonsense_Mutation SNP C C T TCGA-EJ-A7NH-01A-12D-A33T-08 TCGA-EJ-A7NH-10A-01D-A33W-08 g.chrX:15270503C>T c.306G>A c.(304-306)tgG>tgA p.W102* SKCM 23 15266923 15266923 + Missense_Mutation SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chrX:15266923G>A c.703C>T c.(703-705)Cct>Tct p.P235S SKCM 23 15268625 15268625 + Silent SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chrX:15268625G>A c.495C>T c.(493-495)agC>agT p.S165S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BOCA-FR X 15279671 15279671 single base substitution T A intron_variant BOCA-FR X 15279671 15279671 single base substitution T A upstream_gene_variant BOCA-UK X 15268637 15268637 single base substitution G A downstream_gene_variant BOCA-UK X 15268637 15268637 single base substitution G A exon_variant BOCA-UK X 15268637 15268637 single base substitution G A synonymous_variant D151D 453C>T BOCA-UK X 15268637 15268637 single base substitution G A synonymous_variant D161D 483C>T BOCA-UK X 15268637 15268637 single base substitution G A synonymous_variant D76D 228C>T BRCA-EU X 15248985 15248985 single base substitution G A downstream_gene_variant BRCA-EU X 15249532 15249532 single base substitution A C downstream_gene_variant BRCA-EU X 15249876 15249876 single base substitution G A downstream_gene_variant BRCA-EU X 15250117 15250117 single base substitution G A downstream_gene_variant BRCA-EU X 15250894 15250894 single base substitution G C downstream_gene_variant BRCA-EU X 15251734 15251734 single base substitution C A downstream_gene_variant BRCA-EU X 15252001 15252001 single base substitution C T downstream_gene_variant BRCA-EU X 15252349 15252349 single base substitution G A downstream_gene_variant BRCA-EU X 15253504 15253504 single base substitution T C intron_variant BRCA-EU X 15253752 15253752 single base substitution C T intron_variant BRCA-EU X 15253921 15253921 single base substitution G C intron_variant BRCA-EU X 15254115 15254115 single base substitution C G intron_variant BRCA-EU X 15255107 15255107 single base substitution G A intron_variant BRCA-EU X 15255230 15255230 single base substitution A G intron_variant BRCA-EU X 15255555 15255555 single base substitution C G intron_variant BRCA-EU X 15257902 15257902 single base substitution T G downstream_gene_variant BRCA-EU X 15257902 15257902 single base substitution T G intron_variant BRCA-EU X 15259380 15259380 single base substitution C A downstream_gene_variant BRCA-EU X 15259380 15259380 single base substitution C A intron_variant BRCA-EU X 15260859 15260859 single base substitution G T downstream_gene_variant BRCA-EU X 15260859 15260859 single base substitution G T intron_variant BRCA-EU X 15261912 15261912 single base substitution C T downstream_gene_variant BRCA-EU X 15261912 15261912 single base substitution C T intron_variant BRCA-EU X 15262298 15262298 single base substitution G A 3_prime_UTR_variant BRCA-EU X 15262298 15262298 single base substitution G A downstream_gene_variant BRCA-EU X 15262298 15262298 single base substitution G A intron_variant BRCA-EU X 15262744 15262744 single base substitution A T 3_prime_UTR_variant BRCA-EU X 15262744 15262744 single base substitution A T exon_variant BRCA-EU X 15262744 15262744 single base substitution A T intron_variant BRCA-EU X 15262744 15262744 single base substitution A T missense_variant S257T 769T>A BRCA-EU X 15262807 15262807 deletion of <=200bp T - intron_variant BRCA-EU X 15262807 15262807 insertion of <=200bp - T intron_variant BRCA-EU X 15263598 15263598 insertion of <=200bp - C downstream_gene_variant BRCA-EU X 15263598 15263598 insertion of <=200bp - C intron_variant BRCA-EU X 15264789 15264789 single base substitution C T downstream_gene_variant BRCA-EU X 15264789 15264789 single base substitution C T intron_variant BRCA-EU X 15265231 15265231 single base substitution G A downstream_gene_variant BRCA-EU X 15265231 15265231 single base substitution G A intron_variant BRCA-EU X 15265662 15265662 single base substitution G A downstream_gene_variant BRCA-EU X 15265662 15265662 single base substitution G A intron_variant BRCA-EU X 15265867 15265867 single base substitution C T downstream_gene_variant BRCA-EU X 15265867 15265867 single base substitution C T intron_variant BRCA-EU X 15266302 15266302 single base substitution C G downstream_gene_variant BRCA-EU X 15266302 15266302 single base substitution C G intron_variant BRCA-EU X 15267054 15267054 single base substitution G A downstream_gene_variant BRCA-EU X 15267054 15267054 single base substitution G A exon_variant BRCA-EU X 15267054 15267054 single base substitution G A missense_variant A106V 317C>T BRCA-EU X 15267054 15267054 single base substitution G A missense_variant A181V 542C>T BRCA-EU X 15267054 15267054 single base substitution G A missense_variant A191V 572C>T BRCA-EU X 15267403 15267403 single base substitution G T downstream_gene_variant BRCA-EU X 15267403 15267403 single base substitution G T intron_variant BRCA-EU X 15267499 15267499 single base substitution G A downstream_gene_variant BRCA-EU X 15267499 15267499 single base substitution G A intron_variant BRCA-EU X 15267776 15267776 single base substitution A T downstream_gene_variant BRCA-EU X 15267776 15267776 single base substitution A T intron_variant BRCA-EU X 15268371 15268371 single base substitution G C downstream_gene_variant BRCA-EU X 15268371 15268371 single base substitution G C intron_variant BRCA-EU X 15269052 15269052 single base substitution C T intron_variant BRCA-EU X 15269091 15269091 single base substitution C G intron_variant BRCA-EU X 15269634 15269634 single base substitution G A intron_variant BRCA-EU X 15270674 15270674 single base substitution G T intron_variant BRCA-EU X 15273199 15273199 single base substitution G A intron_variant BRCA-EU X 15273199 15273199 single base substitution G A upstream_gene_variant BRCA-EU X 15273747 15273747 single base substitution G A intron_variant BRCA-EU X 15273747 15273747 single base substitution G A upstream_gene_variant BRCA-EU X 15273900 15273900 single base substitution G T intron_variant BRCA-EU X 15273900 15273900 single base substitution G T upstream_gene_variant BRCA-EU X 15274205 15274205 single base substitution C G intron_variant BRCA-EU X 15274205 15274205 single base substitution C G upstream_gene_variant BRCA-EU X 15274351 15274351 single base substitution T C intron_variant BRCA-EU X 15274351 15274351 single base substitution T C upstream_gene_variant BRCA-EU X 15274716 15274716 single base substitution G A intron_variant BRCA-EU X 15274716 15274716 single base substitution G A upstream_gene_variant BRCA-EU X 15275459 15275459 single base substitution C T intron_variant BRCA-EU X 15275459 15275459 single base substitution C T upstream_gene_variant BRCA-EU X 15276502 15276502 single base substitution T G intron_variant BRCA-EU X 15276502 15276502 single base substitution T G upstream_gene_variant BRCA-EU X 15278024 15278024 single base substitution A G intron_variant BRCA-EU X 15278024 15278024 single base substitution A G upstream_gene_variant BRCA-EU X 15278464 15278464 single base substitution G A intron_variant BRCA-EU X 15278464 15278464 single base substitution G A upstream_gene_variant BRCA-EU X 15279353 15279353 single base substitution T A intron_variant BRCA-EU X 15279353 15279353 single base substitution T A upstream_gene_variant BRCA-EU X 15279608 15279608 single base substitution C A intron_variant BRCA-EU X 15279608 15279608 single base substitution C A upstream_gene_variant BRCA-EU X 15279729 15279729 single base substitution G T intron_variant BRCA-EU X 15279729 15279729 single base substitution G T upstream_gene_variant BRCA-EU X 15279943 15279943 single base substitution A T intron_variant BRCA-EU X 15279943 15279943 single base substitution A T upstream_gene_variant BRCA-EU X 15280531 15280531 single base substitution G T intron_variant BRCA-EU X 15280531 15280531 single base substitution G T upstream_gene_variant BRCA-EU X 15280610 15280610 single base substitution G A intron_variant BRCA-EU X 15280610 15280610 single base substitution G A upstream_gene_variant BRCA-EU X 15281520 15281520 single base substitution G A intron_variant BRCA-EU X 15281520 15281520 single base substitution G A upstream_gene_variant BRCA-EU X 15281774 15281774 single base substitution C T intron_variant BRCA-EU X 15281774 15281774 single base substitution C T upstream_gene_variant BRCA-EU X 15282806 15282806 single base substitution G A intron_variant BRCA-EU X 15285009 15285009 single base substitution G T intron_variant BRCA-EU X 15285311 15285311 single base substitution G C intron_variant BRCA-EU X 15285515 15285515 single base substitution G C intron_variant BRCA-EU X 15285857 15285857 single base substitution C A intron_variant BRCA-EU X 15286787 15286787 single base substitution G A intron_variant BRCA-EU X 15287625 15287625 single base substitution A G intron_variant BRCA-EU X 15289059 15289059 single base substitution G A upstream_gene_variant BRCA-EU X 15289364 15289364 single base substitution T C upstream_gene_variant BRCA-EU X 15289670 15289670 single base substitution C T upstream_gene_variant BRCA-EU X 15290902 15290902 single base substitution G T upstream_gene_variant BRCA-EU X 15291136 15291136 single base substitution A T upstream_gene_variant BRCA-EU X 15291269 15291269 single base substitution G A upstream_gene_variant BRCA-EU X 15293209 15293209 single base substitution C T upstream_gene_variant BRCA-FR X 15253921 15253921 single base substitution G T intron_variant BRCA-FR X 15254115 15254115 single base substitution C G intron_variant BRCA-FR X 15255107 15255107 single base substitution G A intron_variant BRCA-FR X 15255127 15255127 single base substitution A G intron_variant BRCA-FR X 15265867 15265867 single base substitution C T downstream_gene_variant BRCA-FR X 15265867 15265867 single base substitution C T intron_variant BRCA-FR X 15266707 15266707 single base substitution T A downstream_gene_variant BRCA-FR X 15266707 15266707 single base substitution T A intron_variant BRCA-FR X 15273747 15273747 single base substitution G A intron_variant BRCA-FR X 15273747 15273747 single base substitution G A upstream_gene_variant BRCA-FR X 15278464 15278464 single base substitution G A intron_variant BRCA-FR X 15278464 15278464 single base substitution G A upstream_gene_variant BRCA-FR X 15280610 15280610 single base substitution G A intron_variant BRCA-FR X 15280610 15280610 single base substitution G A upstream_gene_variant BRCA-FR X 15282806 15282806 single base substitution G A intron_variant BRCA-FR X 15285311 15285311 single base substitution G C intron_variant BRCA-FR X 15290902 15290902 single base substitution G T upstream_gene_variant BRCA-UK X 15259380 15259380 single base substitution C A downstream_gene_variant BRCA-UK X 15259380 15259380 single base substitution C A intron_variant BRCA-UK X 15262554 15262554 single base substitution G C 3_prime_UTR_variant BRCA-UK X 15262554 15262554 single base substitution G C exon_variant BRCA-UK X 15262554 15262554 single base substitution G C intron_variant BRCA-UK X 15267021 15267021 single base substitution G A downstream_gene_variant BRCA-UK X 15267021 15267021 single base substitution G A exon_variant BRCA-UK X 15267021 15267021 single base substitution G A missense_variant P117L 350C>T BRCA-UK X 15267021 15267021 single base substitution G A missense_variant P192L 575C>T BRCA-UK X 15267021 15267021 single base substitution G A missense_variant P202L 605C>T BRCA-UK X 15267499 15267499 single base substitution G A downstream_gene_variant BRCA-UK X 15267499 15267499 single base substitution G A intron_variant BRCA-UK X 15269052 15269052 single base substitution C T intron_variant BRCA-US X 15262576 15262576 single base substitution C A 3_prime_UTR_variant BRCA-US X 15262576 15262576 single base substitution C A exon_variant BRCA-US X 15262576 15262576 single base substitution C A intron_variant BRCA-US X 15262744 15262744 single base substitution A G 3_prime_UTR_variant BRCA-US X 15262744 15262744 single base substitution A G exon_variant BRCA-US X 15262744 15262744 single base substitution A G intron_variant BRCA-US X 15262744 15262744 single base substitution A G missense_variant S257P 769T>C BRCA-US X 15267033 15267033 single base substitution C T downstream_gene_variant BRCA-US X 15267033 15267033 single base substitution C T exon_variant BRCA-US X 15267033 15267033 single base substitution C T missense_variant G113D 338G>A BRCA-US X 15267033 15267033 single base substitution C T missense_variant G188D 563G>A BRCA-US X 15267033 15267033 single base substitution C T missense_variant G198D 593G>A BRCA-US X 15270445 15270445 single base substitution G T exon_variant BRCA-US X 15270445 15270445 single base substitution G T missense_variant L122M 364C>A BRCA-US X 15270445 15270445 single base substitution G T missense_variant L37M 109C>A BRCA-US X 15270445 15270445 single base substitution G T splice_region_variant BRCA-US X 15272920 15272920 single base substitution T C exon_variant BRCA-US X 15272920 15272920 single base substitution T C missense_variant H74R 221A>G BRCA-US X 15272920 15272920 single base substitution T C upstream_gene_variant BTCA-JP X 15262826 15262826 single base substitution G A intron_variant BTCA-JP X 15268682 15268682 single base substitution G A exon_variant BTCA-JP X 15268682 15268682 single base substitution G A intron_variant BTCA-JP X 15268682 15268682 single base substitution G A synonymous_variant H146H 438C>T BTCA-JP X 15268682 15268682 single base substitution G A synonymous_variant H61H 183C>T BTCA-JP X 15272813 15272813 single base substitution C T intron_variant CESC-US X 15266972 15266972 single base substitution G C downstream_gene_variant CESC-US X 15266972 15266972 single base substitution G C exon_variant CESC-US X 15266972 15266972 single base substitution G C synonymous_variant L133L 399C>G CESC-US X 15266972 15266972 single base substitution G C synonymous_variant L208L 624C>G CESC-US X 15266972 15266972 single base substitution G C synonymous_variant L218L 654C>G CLLE-ES X 15251476 15251476 single base substitution A T downstream_gene_variant CLLE-ES X 15270673 15270673 single base substitution G A intron_variant CLLE-ES X 15274970 15274970 single base substitution T A intron_variant CLLE-ES X 15274970 15274970 single base substitution T A upstream_gene_variant COCA-CN X 15262678 15262678 single base substitution T C 3_prime_UTR_variant COCA-CN X 15262678 15262678 single base substitution T C exon_variant COCA-CN X 15262678 15262678 single base substitution T C intron_variant COCA-CN X 15262678 15262678 single base substitution T C missense_variant T279A 835A>G COCA-CN X 15262815 15262815 single base substitution A G intron_variant COCA-CN X 15262834 15262834 single base substitution G T intron_variant COCA-CN X 15270473 15270473 single base substitution G A exon_variant COCA-CN X 15270473 15270473 single base substitution G A intron_variant COCA-CN X 15270473 15270473 single base substitution G A synonymous_variant S112S 336C>T COCA-CN X 15270473 15270473 single base substitution G A synonymous_variant S27S 81C>T EOPC-DE X 15252960 15252960 single base substitution G A downstream_gene_variant GBM-US X 15266989 15266989 single base substitution C A downstream_gene_variant GBM-US X 15266989 15266989 single base substitution C A exon_variant GBM-US X 15266989 15266989 single base substitution C A stop_gained E128* 382G>T GBM-US X 15266989 15266989 single base substitution C A stop_gained E203* 607G>T GBM-US X 15266989 15266989 single base substitution C A stop_gained E213* 637G>T LGG-US X 15272893 15272893 single base substitution G A exon_variant LGG-US X 15272893 15272893 single base substitution G A missense_variant S83F 248C>T LGG-US X 15272893 15272893 single base substitution G A upstream_gene_variant LICA-FR X 15262754 15262754 single base substitution T C intron_variant LICA-FR X 15262754 15262754 single base substitution T C splice_acceptor_variant LICA-FR X 15274898 15274898 deletion of <=200bp A - intron_variant LICA-FR X 15274898 15274898 deletion of <=200bp A - upstream_gene_variant LICA-FR X 15285364 15285364 single base substitution C A intron_variant LICA-FR X 15287969 15287969 single base substitution C A exon_variant LICA-FR X 15287969 15287969 single base substitution C A missense_variant G10W 28G>T LICA-FR X 15292283 15292283 insertion of <=200bp - T upstream_gene_variant LINC-JP X 15262826 15262826 single base substitution G A intron_variant LINC-JP X 15268580 15268580 single base substitution T A downstream_gene_variant LINC-JP X 15268580 15268580 single base substitution T A exon_variant LINC-JP X 15268580 15268580 single base substitution T A missense_variant R170S 510A>T LINC-JP X 15268580 15268580 single base substitution T A missense_variant R180S 540A>T LINC-JP X 15268580 15268580 single base substitution T A missense_variant R95S 285A>T LINC-JP X 15268682 15268682 single base substitution G A exon_variant LINC-JP X 15268682 15268682 single base substitution G A intron_variant LINC-JP X 15268682 15268682 single base substitution G A synonymous_variant H146H 438C>T LINC-JP X 15268682 15268682 single base substitution G A synonymous_variant H61H 183C>T LINC-JP X 15269932 15269932 single base substitution T C intron_variant LINC-JP X 15273107 15273107 deletion of <=200bp A - intron_variant LINC-JP X 15273107 15273107 deletion of <=200bp A - upstream_gene_variant LINC-JP X 15282745 15282745 deletion of <=200bp A - intron_variant LINC-JP X 15285071 15285071 single base substitution A G intron_variant LINC-JP X 15285375 15285375 single base substitution C A intron_variant LINC-JP X 15285527 15285527 single base substitution A G intron_variant LINC-JP X 15285529 15285529 single base substitution C T intron_variant LINC-JP X 15286462 15286462 single base substitution A C intron_variant LINC-JP X 15289247 15289247 single base substitution G A upstream_gene_variant LIRI-JP X 15248643 15248643 single base substitution T C downstream_gene_variant LIRI-JP X 15251927 15251927 single base substitution A G downstream_gene_variant LIRI-JP X 15256684 15256684 single base substitution A C intron_variant LIRI-JP X 15258460 15258460 single base substitution C A downstream_gene_variant LIRI-JP X 15258460 15258460 single base substitution C A intron_variant LIRI-JP X 15259640 15259640 single base substitution T C downstream_gene_variant LIRI-JP X 15259640 15259640 single base substitution T C intron_variant LIRI-JP X 15259866 15259866 single base substitution G T downstream_gene_variant LIRI-JP X 15259866 15259866 single base substitution G T intron_variant LIRI-JP X 15263864 15263864 single base substitution G A downstream_gene_variant LIRI-JP X 15263864 15263864 single base substitution G A intron_variant LIRI-JP X 15267137 15267137 single base substitution A G downstream_gene_variant LIRI-JP X 15267137 15267137 single base substitution A G intron_variant LIRI-JP X 15268974 15268974 single base substitution C A intron_variant LIRI-JP X 15273626 15273626 single base substitution A C intron_variant LIRI-JP X 15273626 15273626 single base substitution A C upstream_gene_variant LIRI-JP X 15273683 15273683 single base substitution T G intron_variant LIRI-JP X 15273683 15273683 single base substitution T G upstream_gene_variant LIRI-JP X 15278193 15278193 single base substitution T C intron_variant LIRI-JP X 15278193 15278193 single base substitution T C upstream_gene_variant LIRI-JP X 15279039 15279039 single base substitution C A intron_variant LIRI-JP X 15279039 15279039 single base substitution C A upstream_gene_variant LIRI-JP X 15283156 15283156 single base substitution G T intron_variant LIRI-JP X 15285090 15285090 insertion of <=200bp - G intron_variant LIRI-JP X 15287567 15287567 single base substitution T C intron_variant LIRI-JP X 15287848 15287848 single base substitution C G intron_variant LIRI-JP X 15288693 15288693 deletion of <=200bp T - upstream_gene_variant LIRI-JP X 15292977 15292977 single base substitution G T upstream_gene_variant LUSC-KR X 15249240 15249240 single base substitution C A downstream_gene_variant LUSC-KR X 15251134 15251134 single base substitution C A downstream_gene_variant LUSC-KR X 15254257 15254257 single base substitution G T intron_variant LUSC-KR X 15257456 15257456 single base substitution C A downstream_gene_variant LUSC-KR X 15257456 15257456 single base substitution C A intron_variant LUSC-KR X 15261455 15261455 single base substitution G C downstream_gene_variant LUSC-KR X 15261455 15261455 single base substitution G C intron_variant LUSC-KR X 15281511 15281511 single base substitution T A intron_variant LUSC-KR X 15281511 15281511 single base substitution T A upstream_gene_variant LUSC-KR X 15281527 15281527 single base substitution C A intron_variant LUSC-KR X 15281527 15281527 single base substitution C A upstream_gene_variant LUSC-KR X 15283079 15283079 single base substitution C T intron_variant LUSC-KR X 15293308 15293308 single base substitution C A upstream_gene_variant LUSC-US X 15268561 15268561 single base substitution G C downstream_gene_variant LUSC-US X 15268561 15268561 single base substitution G C exon_variant LUSC-US X 15268561 15268561 single base substitution G C missense_variant L102V 304C>G LUSC-US X 15268561 15268561 single base substitution G C missense_variant L177V 529C>G LUSC-US X 15268561 15268561 single base substitution G C missense_variant L187V 559C>G LUSC-US X 15268612 15268612 single base substitution G T downstream_gene_variant LUSC-US X 15268612 15268612 single base substitution G T exon_variant LUSC-US X 15268612 15268612 single base substitution G T missense_variant P160T 478C>A LUSC-US X 15268612 15268612 single base substitution G T missense_variant P170T 508C>A LUSC-US X 15268612 15268612 single base substitution G T missense_variant P85T 253C>A LUSC-US X 15270382 15270382 single base substitution T A exon_variant LUSC-US X 15270382 15270382 single base substitution T A missense_variant R143W 427A>T LUSC-US X 15270382 15270382 single base substitution T A missense_variant R58W 172A>T LUSC-US X 15287980 15287980 single base substitution C A exon_variant LUSC-US X 15287980 15287980 single base substitution C A missense_variant G6V 17G>T LUSC-US X 15287981 15287981 single base substitution C G exon_variant LUSC-US X 15287981 15287981 single base substitution C G missense_variant G6R 16G>C MALY-DE X 15265595 15265595 single base substitution C T downstream_gene_variant MALY-DE X 15265595 15265595 single base substitution C T intron_variant MALY-DE X 15268327 15268327 single base substitution T A downstream_gene_variant MALY-DE X 15268327 15268327 single base substitution T A intron_variant MALY-DE X 15272255 15272255 single base substitution C T intron_variant MALY-DE X 15275534 15275534 single base substitution T A intron_variant MALY-DE X 15275534 15275534 single base substitution T A upstream_gene_variant MALY-DE X 15281317 15281317 single base substitution C A intron_variant MALY-DE X 15281317 15281317 single base substitution C A upstream_gene_variant MALY-DE X 15283741 15283741 single base substitution C T intron_variant MALY-DE X 15283744 15283744 single base substitution C T intron_variant MALY-DE X 15287633 15287633 single base substitution G A intron_variant MALY-DE X 15289530 15289530 single base substitution C A upstream_gene_variant MALY-DE X 15290123 15290123 single base substitution G A upstream_gene_variant MALY-DE X 15293376 15293376 single base substitution C G upstream_gene_variant MELA-AU X 15248599 15248599 single base substitution G A downstream_gene_variant MELA-AU X 15250075 15250075 single base substitution C T downstream_gene_variant MELA-AU X 15252494 15252494 single base substitution C T downstream_gene_variant MELA-AU X 15253693 15253693 single base substitution C A intron_variant MELA-AU X 15254021 15254021 single base substitution C T intron_variant MELA-AU X 15254632 15254632 single base substitution G A intron_variant MELA-AU X 15254744 15254744 single base substitution G A intron_variant MELA-AU X 15255191 15255191 single base substitution C T intron_variant MELA-AU X 15255980 15255980 single base substitution G A intron_variant MELA-AU X 15256201 15256201 single base substitution G A intron_variant MELA-AU X 15256347 15256347 single base substitution C T intron_variant MELA-AU X 15256860 15256860 single base substitution T C intron_variant MELA-AU X 15257949 15257949 single base substitution G A downstream_gene_variant MELA-AU X 15257949 15257949 single base substitution G A intron_variant MELA-AU X 15258008 15258008 single base substitution C T downstream_gene_variant MELA-AU X 15258008 15258008 single base substitution C T intron_variant MELA-AU X 15258404 15258404 single base substitution G A downstream_gene_variant MELA-AU X 15258404 15258404 single base substitution G A intron_variant MELA-AU X 15258807 15258807 single base substitution G A downstream_gene_variant MELA-AU X 15258807 15258807 single base substitution G A intron_variant MELA-AU X 15258836 15258836 single base substitution G C downstream_gene_variant MELA-AU X 15258836 15258836 single base substitution G C intron_variant MELA-AU X 15259191 15259191 single base substitution C T downstream_gene_variant MELA-AU X 15259191 15259191 single base substitution C T intron_variant MELA-AU X 15259226 15259226 single base substitution G A downstream_gene_variant MELA-AU X 15259226 15259226 single base substitution G A intron_variant MELA-AU X 15259575 15259575 single base substitution C T downstream_gene_variant MELA-AU X 15259575 15259575 single base substitution C T intron_variant MELA-AU X 15259633 15259633 single base substitution G A downstream_gene_variant MELA-AU X 15259633 15259633 single base substitution G A intron_variant MELA-AU X 15260382 15260382 single base substitution G A downstream_gene_variant MELA-AU X 15260382 15260382 single base substitution G A intron_variant MELA-AU X 15260970 15260970 single base substitution C T downstream_gene_variant MELA-AU X 15260970 15260970 single base substitution C T intron_variant MELA-AU X 15261242 15261242 single base substitution C T downstream_gene_variant MELA-AU X 15261242 15261242 single base substitution C T intron_variant MELA-AU X 15261556 15261556 single base substitution C T downstream_gene_variant MELA-AU X 15261556 15261556 single base substitution C T intron_variant MELA-AU X 15262520 15262520 single base substitution C T 3_prime_UTR_variant MELA-AU X 15262520 15262520 single base substitution C T exon_variant MELA-AU X 15262520 15262520 single base substitution C T intron_variant MELA-AU X 15263593 15263593 insertion of <=200bp - CCCTGCCC downstream_gene_variant MELA-AU X 15263593 15263593 insertion of <=200bp - CCCTGCCC intron_variant MELA-AU X 15264721 15264722 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU X 15264721 15264722 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 15266003 15266003 single base substitution G C downstream_gene_variant MELA-AU X 15266003 15266003 single base substitution G C intron_variant MELA-AU X 15266158 15266158 single base substitution T C downstream_gene_variant MELA-AU X 15266158 15266158 single base substitution T C intron_variant MELA-AU X 15266321 15266321 single base substitution C T downstream_gene_variant MELA-AU X 15266321 15266321 single base substitution C T intron_variant MELA-AU X 15266650 15266650 single base substitution G A downstream_gene_variant MELA-AU X 15266650 15266650 single base substitution G A intron_variant MELA-AU X 15266732 15266732 single base substitution A G downstream_gene_variant MELA-AU X 15266732 15266732 single base substitution A G intron_variant MELA-AU X 15267443 15267443 single base substitution A T downstream_gene_variant MELA-AU X 15267443 15267443 single base substitution A T intron_variant MELA-AU X 15267523 15267523 single base substitution A G downstream_gene_variant MELA-AU X 15267523 15267523 single base substitution A G intron_variant MELA-AU X 15268167 15268167 single base substitution G A downstream_gene_variant MELA-AU X 15268167 15268167 single base substitution G A intron_variant MELA-AU X 15268577 15268577 single base substitution G A downstream_gene_variant MELA-AU X 15268577 15268577 single base substitution G A exon_variant MELA-AU X 15268577 15268577 single base substitution G A synonymous_variant A171A 513C>T MELA-AU X 15268577 15268577 single base substitution G A synonymous_variant A181A 543C>T MELA-AU X 15268577 15268577 single base substitution G A synonymous_variant A96A 288C>T MELA-AU X 15268760 15268760 single base substitution T C intron_variant MELA-AU X 15268868 15268868 single base substitution G A intron_variant MELA-AU X 15268960 15268960 single base substitution C T intron_variant MELA-AU X 15269001 15269001 single base substitution C T intron_variant MELA-AU X 15269152 15269152 single base substitution G A intron_variant MELA-AU X 15269820 15269820 single base substitution A G intron_variant MELA-AU X 15270590 15270590 single base substitution C T intron_variant MELA-AU X 15270792 15270792 single base substitution C T intron_variant MELA-AU X 15270897 15270897 single base substitution G A intron_variant MELA-AU X 15271131 15271131 single base substitution G A intron_variant MELA-AU X 15271339 15271339 single base substitution G A intron_variant MELA-AU X 15272151 15272151 single base substitution C T intron_variant MELA-AU X 15272800 15272800 single base substitution G A intron_variant MELA-AU X 15273329 15273329 single base substitution G A intron_variant MELA-AU X 15273329 15273329 single base substitution G A upstream_gene_variant MELA-AU X 15273634 15273634 single base substitution G A intron_variant MELA-AU X 15273634 15273634 single base substitution G A upstream_gene_variant MELA-AU X 15274172 15274172 single base substitution G A intron_variant MELA-AU X 15274172 15274172 single base substitution G A upstream_gene_variant MELA-AU X 15274510 15274510 single base substitution G A intron_variant MELA-AU X 15274510 15274510 single base substitution G A upstream_gene_variant MELA-AU X 15275449 15275449 single base substitution A G intron_variant MELA-AU X 15275449 15275449 single base substitution A G upstream_gene_variant MELA-AU X 15276578 15276578 single base substitution G A intron_variant MELA-AU X 15276578 15276578 single base substitution G A upstream_gene_variant MELA-AU X 15277164 15277164 single base substitution G A exon_variant MELA-AU X 15277164 15277164 single base substitution G A intron_variant MELA-AU X 15277164 15277164 single base substitution G A upstream_gene_variant MELA-AU X 15277169 15277169 single base substitution G A exon_variant MELA-AU X 15277169 15277169 single base substitution G A intron_variant MELA-AU X 15277169 15277169 single base substitution G A upstream_gene_variant MELA-AU X 15277817 15277818 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 15277817 15277818 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 15278245 15278245 single base substitution G A intron_variant MELA-AU X 15278245 15278245 single base substitution G A upstream_gene_variant MELA-AU X 15278861 15278861 single base substitution G A intron_variant MELA-AU X 15278861 15278861 single base substitution G A upstream_gene_variant MELA-AU X 15279225 15279225 single base substitution C T intron_variant MELA-AU X 15279225 15279225 single base substitution C T upstream_gene_variant MELA-AU X 15281505 15281505 single base substitution C T intron_variant MELA-AU X 15281505 15281505 single base substitution C T upstream_gene_variant MELA-AU X 15282513 15282513 single base substitution C T intron_variant MELA-AU X 15282765 15282765 single base substitution G A intron_variant MELA-AU X 15282908 15282908 single base substitution G A intron_variant MELA-AU X 15283257 15283257 single base substitution C T intron_variant MELA-AU X 15283736 15283736 single base substitution G A intron_variant MELA-AU X 15284029 15284029 single base substitution G A intron_variant MELA-AU X 15285107 15285107 single base substitution G A intron_variant MELA-AU X 15285375 15285375 single base substitution C A intron_variant MELA-AU X 15285466 15285466 single base substitution G A intron_variant MELA-AU X 15286202 15286202 single base substitution C T intron_variant MELA-AU X 15286792 15286792 single base substitution G A intron_variant MELA-AU X 15287113 15287113 single base substitution C T intron_variant MELA-AU X 15287838 15287838 single base substitution A G intron_variant MELA-AU X 15289271 15289271 single base substitution C T upstream_gene_variant MELA-AU X 15291003 15291003 single base substitution C A upstream_gene_variant MELA-AU X 15291565 15291565 single base substitution A T upstream_gene_variant MELA-AU X 15291608 15291608 single base substitution C T upstream_gene_variant MELA-AU X 15291779 15291780 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 15292105 15292105 single base substitution G A upstream_gene_variant MELA-AU X 15292810 15292810 single base substitution T G upstream_gene_variant MELA-AU X 15293319 15293319 single base substitution G A upstream_gene_variant ORCA-IN X 15270483 15270483 single base substitution G T exon_variant ORCA-IN X 15270483 15270483 single base substitution G T intron_variant ORCA-IN X 15270483 15270483 single base substitution G T missense_variant A109D 326C>A ORCA-IN X 15270483 15270483 single base substitution G T missense_variant A24D 71C>A OV-AU X 15255740 15255740 single base substitution C T intron_variant OV-AU X 15256019 15256019 single base substitution G A intron_variant OV-AU X 15279131 15279131 single base substitution G C intron_variant OV-AU X 15279131 15279131 single base substitution G C upstream_gene_variant OV-AU X 15280251 15280251 single base substitution T C intron_variant OV-AU X 15280251 15280251 single base substitution T C upstream_gene_variant OV-AU X 15280622 15280622 single base substitution T C intron_variant OV-AU X 15280622 15280622 single base substitution T C upstream_gene_variant OV-AU X 15284627 15284627 single base substitution G C intron_variant OV-AU X 15285072 15285072 single base substitution A G intron_variant OV-AU X 15290949 15290949 single base substitution G T upstream_gene_variant PACA-AU X 15250093 15250093 single base substitution C T downstream_gene_variant PACA-AU X 15258010 15258010 single base substitution G A downstream_gene_variant PACA-AU X 15258010 15258010 single base substitution G A intron_variant PACA-AU X 15258497 15258497 single base substitution A G downstream_gene_variant PACA-AU X 15258497 15258497 single base substitution A G intron_variant PACA-AU X 15258666 15258666 single base substitution C T downstream_gene_variant PACA-AU X 15258666 15258666 single base substitution C T intron_variant PACA-AU X 15272805 15272805 single base substitution T C intron_variant PACA-AU X 15273523 15273523 single base substitution G C intron_variant PACA-AU X 15273523 15273523 single base substitution G C upstream_gene_variant PACA-AU X 15273943 15273943 single base substitution T C intron_variant PACA-AU X 15273943 15273943 single base substitution T C upstream_gene_variant PACA-AU X 15274279 15274279 single base substitution T C intron_variant PACA-AU X 15274279 15274279 single base substitution T C upstream_gene_variant PACA-AU X 15279183 15279183 single base substitution G A intron_variant PACA-AU X 15279183 15279183 single base substitution G A upstream_gene_variant PACA-AU X 15288941 15288941 single base substitution G A upstream_gene_variant PACA-CA X 15252584 15252584 single base substitution A G downstream_gene_variant PACA-CA X 15252909 15252909 single base substitution G A downstream_gene_variant PACA-CA X 15253758 15253758 single base substitution A C intron_variant PACA-CA X 15254847 15254847 single base substitution G A intron_variant PACA-CA X 15266314 15266314 single base substitution A G downstream_gene_variant PACA-CA X 15266314 15266314 single base substitution A G intron_variant PACA-CA X 15268332 15268332 single base substitution C A downstream_gene_variant PACA-CA X 15268332 15268332 single base substitution C A intron_variant PACA-CA X 15268939 15268939 single base substitution G A intron_variant PACA-CA X 15275531 15275531 single base substitution A T intron_variant PACA-CA X 15275531 15275531 single base substitution A T upstream_gene_variant PACA-CA X 15275705 15275705 single base substitution T A intron_variant PACA-CA X 15275705 15275705 single base substitution T A upstream_gene_variant PACA-CA X 15276589 15276589 single base substitution A T intron_variant PACA-CA X 15276589 15276589 single base substitution A T upstream_gene_variant PACA-CA X 15276754 15276754 single base substitution G A intron_variant PACA-CA X 15276754 15276754 single base substitution G A upstream_gene_variant PACA-CA X 15278246 15278246 single base substitution C T intron_variant PACA-CA X 15278246 15278246 single base substitution C T upstream_gene_variant PACA-CA X 15279835 15279835 single base substitution G A intron_variant PACA-CA X 15279835 15279835 single base substitution G A upstream_gene_variant PACA-CA X 15283191 15283191 single base substitution A G intron_variant PACA-CA X 15284223 15284223 single base substitution T A intron_variant PACA-CA X 15284224 15284224 single base substitution C G intron_variant PACA-CA X 15285465 15285465 single base substitution C T intron_variant PACA-CA X 15285537 15285537 insertion of <=200bp - TAT intron_variant PACA-CA X 15285539 15285539 single base substitution A T intron_variant PACA-CA X 15293209 15293209 single base substitution C T upstream_gene_variant PAEN-AU X 15271200 15271200 single base substitution C T intron_variant PAEN-AU X 15280464 15280464 single base substitution A G intron_variant PAEN-AU X 15280464 15280464 single base substitution A G upstream_gene_variant PAEN-AU X 15281823 15281823 single base substitution G T intron_variant PAEN-AU X 15281823 15281823 single base substitution G T upstream_gene_variant PAEN-IT X 15275175 15275175 single base substitution G A intron_variant PAEN-IT X 15275175 15275175 single base substitution G A upstream_gene_variant PBCA-DE X 15254170 15254170 deletion of <=200bp A - intron_variant PBCA-DE X 15255156 15255156 deletion of <=200bp T - intron_variant PBCA-DE X 15270817 15270817 single base substitution T A intron_variant PBCA-DE X 15281888 15281888 single base substitution T A intron_variant PBCA-DE X 15281888 15281888 single base substitution T A upstream_gene_variant PBCA-DE X 15288204 15288205 deletion of <=200bp AC - 5_prime_UTR_variant PBCA-DE X 15288204 15288205 deletion of <=200bp AC - intron_variant PBCA-DE X 15288204 15288205 deletion of <=200bp AC - upstream_gene_variant PBCA-DE X 15293209 15293209 single base substitution C T upstream_gene_variant PBCA-DE X 15293405 15293405 single base substitution C T upstream_gene_variant PRAD-CA X 15260245 15260245 single base substitution T A downstream_gene_variant PRAD-CA X 15260245 15260245 single base substitution T A intron_variant PRAD-CA X 15278675 15278675 single base substitution C T intron_variant PRAD-CA X 15278675 15278675 single base substitution C T upstream_gene_variant PRAD-CA X 15287348 15287348 single base substitution C A intron_variant PRAD-UK X 15260307 15260307 single base substitution A T downstream_gene_variant PRAD-UK X 15260307 15260307 single base substitution A T intron_variant PRAD-UK X 15268988 15268988 single base substitution G A intron_variant PRAD-UK X 15291514 15291514 single base substitution A G upstream_gene_variant RECA-EU X 15256424 15256424 single base substitution A C intron_variant RECA-EU X 15268335 15268335 single base substitution C A downstream_gene_variant RECA-EU X 15268335 15268335 single base substitution C A intron_variant RECA-EU X 15281646 15281646 single base substitution C A intron_variant RECA-EU X 15281646 15281646 single base substitution C A upstream_gene_variant RECA-EU X 15290939 15290939 single base substitution G A upstream_gene_variant SKCA-BR X 15248439 15248439 single base substitution C T downstream_gene_variant SKCA-BR X 15253886 15253886 single base substitution A G intron_variant SKCA-BR X 15262813 15262813 insertion of <=200bp - TG intron_variant SKCA-BR X 15266065 15266065 single base substitution C G downstream_gene_variant SKCA-BR X 15266065 15266065 single base substitution C G intron_variant SKCA-BR X 15269432 15269432 single base substitution G A intron_variant SKCA-BR X 15269842 15269842 single base substitution G A intron_variant SKCA-BR X 15273380 15273380 single base substitution A G intron_variant SKCA-BR X 15273380 15273380 single base substitution A G upstream_gene_variant SKCA-BR X 15274422 15274422 single base substitution G A intron_variant SKCA-BR X 15274422 15274422 single base substitution G A upstream_gene_variant SKCA-BR X 15274917 15274917 single base substitution G A intron_variant SKCA-BR X 15274917 15274917 single base substitution G A upstream_gene_variant SKCA-BR X 15274921 15274921 single base substitution G A intron_variant SKCA-BR X 15274921 15274921 single base substitution G A upstream_gene_variant SKCA-BR X 15281916 15281916 single base substitution C T intron_variant SKCA-BR X 15281916 15281916 single base substitution C T upstream_gene_variant SKCA-BR X 15285302 15285302 single base substitution T C intron_variant SKCA-BR X 15285878 15285878 single base substitution A C intron_variant SKCA-BR X 15292531 15292531 single base substitution C T upstream_gene_variant SKCM-US X 15266923 15266923 single base substitution G A downstream_gene_variant SKCM-US X 15266923 15266923 single base substitution G A exon_variant SKCM-US X 15266923 15266923 single base substitution G A missense_variant P150S 448C>T SKCM-US X 15266923 15266923 single base substitution G A missense_variant P225S 673C>T SKCM-US X 15266923 15266923 single base substitution G A missense_variant P235S 703C>T SKCM-US X 15268625 15268625 single base substitution G A downstream_gene_variant SKCM-US X 15268625 15268625 single base substitution G A exon_variant SKCM-US X 15268625 15268625 single base substitution G A synonymous_variant S155S 465C>T SKCM-US X 15268625 15268625 single base substitution G A synonymous_variant S165S 495C>T SKCM-US X 15268625 15268625 single base substitution G A synonymous_variant S80S 240C>T STAD-US X 15267048 15267048 single base substitution A G downstream_gene_variant STAD-US X 15267048 15267048 single base substitution A G exon_variant STAD-US X 15267048 15267048 single base substitution A G missense_variant V108A 323T>C STAD-US X 15267048 15267048 single base substitution A G missense_variant V183A 548T>C STAD-US X 15267048 15267048 single base substitution A G missense_variant V193A 578T>C STAD-US X 15268632 15268632 single base substitution T G downstream_gene_variant STAD-US X 15268632 15268632 single base substitution T G exon_variant STAD-US X 15268632 15268632 single base substitution T G missense_variant K153T 458A>C STAD-US X 15268632 15268632 single base substitution T G missense_variant K163T 488A>C STAD-US X 15268632 15268632 single base substitution T G missense_variant K78T 233A>C STAD-US X 15287932 15287932 single base substitution A C exon_variant STAD-US X 15287932 15287932 single base substitution A C missense_variant I22S 65T>G STAD-US X 15287958 15287958 single base substitution G A exon_variant STAD-US X 15287958 15287958 single base substitution G A synonymous_variant P13P 39C>T UCEC-US X 15262645 15262645 single base substitution A G 3_prime_UTR_variant UCEC-US X 15262645 15262645 single base substitution A G exon_variant UCEC-US X 15262645 15262645 single base substitution A G intron_variant UCEC-US X 15262645 15262645 single base substitution A G missense_variant F290L 868T>C UCEC-US X 15266968 15266968 single base substitution C T downstream_gene_variant UCEC-US X 15266968 15266968 single base substitution C T exon_variant UCEC-US X 15266968 15266968 single base substitution C T missense_variant D135N 403G>A UCEC-US X 15266968 15266968 single base substitution C T missense_variant D210N 628G>A UCEC-US X 15266968 15266968 single base substitution C T missense_variant D220N 658G>A UCEC-US X 15270503 15270503 single base substitution C T exon_variant UCEC-US X 15270503 15270503 single base substitution C T intron_variant UCEC-US X 15270503 15270503 single base substitution C T stop_gained W102* 306G>A UCEC-US X 15270503 15270503 single base substitution C T stop_gained W17* 51G>A UCEC-US X 15287989 15287989 single base substitution C T exon_variant UCEC-US X 15287989 15287989 single base substitution C T missense_variant G3D 8G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC124 COSM1625654 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - TCGA-60-2722-01 COSM1151528 c.559C>G p.L187V Substitution - Missense 23:15250439-15250439 - TCGA-BR-8589-01 COSM4107662 c.488A>C p.K163T Substitution - Missense 23:15250510-15250510 - PT49 COSM5936757 c.403G>A p.A135T Substitution - Missense 23:15252284-15252284 - BZ23 COSM5758629 c.342C>G p.S114R Substitution - Missense 23:15252345-15252345 - TCGA-CG-4305-01 COSM4107781 c.65T>G p.I22S Substitution - Missense 23:15269810-15269810 - sysucc-311T COSM5467844 c.336C>T p.S112S Substitution - coding silent 23:15252351-15252351 - TCGA-FS-A4F5-06 COSM3559415 c.703C>T p.P235S Substitution - Missense 23:15248801-15248801 - TCGA-HJ-7597-01 COSM4107783 c.39C>T p.P13P Substitution - coding silent 23:15269836-15269836 - S01861 COSM5671488 c.290G>T p.G97V Substitution - Missense 23:15252397-15252397 - TCGA-HJ-7597-01 COSM4107782 c.39C>T p.P13P Substitution - coding silent 23:15269836-15269836 - 545 COSM5611626 c.577G>A p.V193M Substitution - Missense 23:15248927-15248927 - 115 COSM5013714 c.155T>C p.L52P Substitution - Missense 23:15258885-15258885 - 545 COSM5611625 c.577G>A p.V193M Substitution - Missense 23:15248927-15248927 - TCGA-D1-A16Y-01 COSM1117442 c.8G>A p.G3D Substitution - Missense 23:15269867-15269867 - CHC327T COSM4950582 c.761-2A>G p.? Unknown 23:15244632-15244632 - TCGA-56-6545-01 COSM755775 c.17G>T p.G6V Substitution - Missense 23:15269858-15269858 - TCGA-B5-A11E-01 COSM1117263 c.658G>A p.D220N Substitution - Missense 23:15248846-15248846 - sysucc-311T COSM5467843 c.336C>T p.S112S Substitution - coding silent 23:15252351-15252351 - BZ23 COSM5758630 c.342C>G p.S114R Substitution - Missense 23:15252345-15252345 - 115 COSM5013713 c.155T>C p.L52P Substitution - Missense 23:15258885-15258885 - CSCC-16-T COSM4506834 c.730C>T p.P244S Substitution - Missense 23:15248774-15248774 - 53M COSM5594227 c.212C>T p.S71F Substitution - Missense 23:15254807-15254807 - YUOTHO COSM5412264 c.280C>T p.Q94* Substitution - Nonsense 23:15254739-15254739 - TCGA-D1-A16Y-01 COSM1599051 c.8G>A p.G3D Substitution - Missense 23:15269867-15269867 - YUOTHO COSM5412265 c.280C>T p.Q94* Substitution - Nonsense 23:15254739-15254739 - CSCC-27-T COSM4454833 c.590A>T p.K197I Substitution - Missense 23:15248914-15248914 - PT49 COSM5936756 c.403G>A p.A135T Substitution - Missense 23:15252284-15252284 - CSCC-11-T COSM4531210 c.176G>A p.G59E Substitution - Missense 23:15254843-15254843 - C135 COSM4618905 c.170G>A p.S57N Substitution - Missense 23:15258870-15258870 - TCGA-CG-4305-01 COSM4107780 c.65T>G p.I22S Substitution - Missense 23:15269810-15269810 - 53M COSM5594228 c.212C>T p.S71F Substitution - Missense 23:15254807-15254807 - PD9573a COSM5618173 c.572C>T p.A191V Substitution - Missense 23:15248932-15248932 - CSCC-16-T COSM4506835 c.730C>T p.P244S Substitution - Missense 23:15248774-15248774 - HCC2998 COSM1682411 c.799C>T p.R267W Substitution - Missense 23:15244592-15244592 - Pat_70_A COSM5877331 c.766C>T p.P256S Substitution - Missense 23:15244625-15244625 - HCC2998 COSM3235295 c.140G>A p.G47E Substitution - Missense 23:15258900-15258900 - HCC158 COSM3708502 c.540A>T p.R180S Substitution - Missense 23:15250458-15250458 - S02277 COSM5683377 c.198G>T p.T66T Substitution - coding silent 23:15254821-15254821 - TCGA-BR-8680-01 COSM4107660 c.578T>C p.V193A Substitution - Missense 23:15248926-15248926 - HCC158T COSM3708501 c.540A>T p.R180S Substitution - Missense 23:15250458-15250458 - CSCC-11-T COSM4531211 c.176G>A p.G59E Substitution - Missense 23:15254843-15254843 - TCGA-D1-A16F-01 COSM1598988 c.306G>A p.W102* Substitution - Nonsense 23:15252381-15252381 - SJDOSTEOS007 COSM5759946 c.700C>T p.R234C Substitution - Missense 23:15248804-15248804 - TCGA-BR-8680-01 COSM4107659 c.578T>C p.V193A Substitution - Missense 23:15248926-15248926 - 2492730 COSM5728289 c.116C>T p.P39L Substitution - Missense 23:15258924-15258924 - PD9573a COSM5618174 c.572C>T p.A191V Substitution - Missense 23:15248932-15248932 - sysucc-1247T COSM5764728 c.835A>G p.T279A Substitution - Missense 23:15244556-15244556 - TCGA-DU-5855-01 COSM3973410 c.248C>T p.S83F Substitution - Missense 23:15254771-15254771 - TCGA-AN-A046-01 COSM3843949 c.364C>A p.L122M Substitution - Missense 23:15252323-15252323 - CSCC-55-T COSM4544347 c.354G>A p.V118V Substitution - coding silent 23:15252333-15252333 - T2940 COSM4663659 c.424G>T p.A142S Substitution - Missense 23:15252263-15252263 - HCC158T COSM3708502 c.540A>T p.R180S Substitution - Missense 23:15250458-15250458 - C086 COSM1145634 c.747C>T p.F249F Substitution - coding silent 23:15248757-15248757 - TCGA-D3-A3ML-06 COSM3559416 c.495C>T p.S165S Substitution - coding silent 23:15250503-15250503 - PD6351a COSM1636970 c.483C>T p.D161D Substitution - coding silent 23:15250515-15250515 - CSCC-60-T COSM1598989 c.658G>A p.D220N Substitution - Missense 23:15248846-15248846 - TCGA-CJ-5681-01 COSM488127 c.29G>C p.G10A Substitution - Missense 23:15269846-15269846 - SJDOSTEOS007 COSM5759945 c.700C>T p.R234C Substitution - Missense 23:15248804-15248804 - PT13 COSM5896474 c.115C>T p.P39S Substitution - Missense 23:15258925-15258925 - TCGA-DR-A0ZM-01 COSM462290 c.654C>G p.L218L Substitution - coding silent 23:15248850-15248850 - S02277 COSM5683376 c.198G>T p.T66T Substitution - coding silent 23:15254821-15254821 - TCGA-D3-A3ML-06 COSM3559417 c.495C>T p.S165S Substitution - coding silent 23:15250503-15250503 - TCGA-AN-A046-01 COSM3843950 c.364C>A p.L122M Substitution - Missense 23:15252323-15252323 - TCGA-D1-A16F-01 COSM1117279 c.306G>A p.W102* Substitution - Nonsense 23:15252381-15252381 - TCGA-A2-A04P-01 COSM1490620 c.593G>A p.G198D Substitution - Missense 23:15248911-15248911 - C086 COSM611520 c.747C>T p.F249F Substitution - coding silent 23:15248757-15248757 - Pat_24_B COSM5877334 c.436C>T p.H146Y Substitution - Missense 23:15250562-15250562 - CSCC-27-T COSM4454832 c.590A>T p.K197I Substitution - Missense 23:15248914-15248914 - TCGA-56-6545-01 COSM1151532 c.17G>T p.G6V Substitution - Missense 23:15269858-15269858 - CSCC-60-T COSM1117263 c.658G>A p.D220N Substitution - Missense 23:15248846-15248846 - TCGA-21-1070-01 COSM1151529 c.508C>A p.P170T Substitution - Missense 23:15250490-15250490 - BD236T COSM1625653 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - TCGA-FS-A4F5-06 COSM3559414 c.703C>T p.P235S Substitution - Missense 23:15248801-15248801 - TCGA-76-4931-01 COSM3406097 c.637G>T p.E213* Substitution - Nonsense 23:15248867-15248867 - HCC2998 COSM3235296 c.140G>A p.G47E Substitution - Missense 23:15258900-15258900 - TCGA-B5-A11E-01 COSM1598989 c.658G>A p.D220N Substitution - Missense 23:15248846-15248846 - PT13 COSM5896475 c.115C>T p.P39S Substitution - Missense 23:15258925-15258925 - HCC2998 COSM3235238 c.776A>C p.K259T Substitution - Missense 23:15248728-15248728 - TCGA-A8-A06Z-01 COSM1490623 c.221A>G p.H74R Substitution - Missense 23:15254798-15254798 - TCGA-A8-A06Z-01 COSM457016 c.221A>G p.H74R Substitution - Missense 23:15254798-15254798 - BD236T COSM1625654 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - PD4954a COSM5799275 c.769T>A p.S257T Substitution - Missense 23:15244622-15244622 - TCGA-E9-A22E-01 COSM1490619 c.769T>C p.S257P Substitution - Missense 23:15244622-15244622 - HCC124T COSM1625654 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - HCC124 COSM1625653 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - TCGA-22-5492-01 COSM755820 c.427A>T p.R143W Substitution - Missense 23:15252260-15252260 - TCGA-22-5492-01 COSM1151530 c.427A>T p.R143W Substitution - Missense 23:15252260-15252260 - HCC2998 COSM1682411 c.799C>T p.R267W Substitution - Missense 23:15244592-15244592 - TCGA-76-4931-01 COSM3406098 c.637G>T p.E213* Substitution - Nonsense 23:15248867-15248867 - CSCC-55-T COSM4544346 c.354G>A p.V118V Substitution - coding silent 23:15252333-15252333 - HCC158 COSM3708501 c.540A>T p.R180S Substitution - Missense 23:15250458-15250458 - T23 COSM5618173 c.572C>T p.A191V Substitution - Missense 23:15248932-15248932 - TCGA-56-6545-01 COSM755773 c.16G>C p.G6R Substitution - Missense 23:15269859-15269859 - CHC327T COSM4950582 c.761-2A>G p.? Unknown 23:15244632-15244632 - PD6351a COSM1636969 c.483C>T p.D161D Substitution - coding silent 23:15250515-15250515 - TCGA-BR-8589-01 COSM4107661 c.488A>C p.K163T Substitution - Missense 23:15250510-15250510 - TCGA-21-1070-01 COSM755821 c.508C>A p.P170T Substitution - Missense 23:15250490-15250490 - TCGA-DR-A0ZM-01 COSM1134633 c.654C>G p.L218L Substitution - coding silent 23:15248850-15248850 - TCGA-DU-5855-01 COSM3973411 c.248C>T p.S83F Substitution - Missense 23:15254771-15254771 - TCGA-A2-A04P-01 COSM457010 c.593G>A p.G198D Substitution - Missense 23:15248911-15248911 - TCGA-60-2722-01 COSM755822 c.559C>G p.L187V Substitution - Missense 23:15250439-15250439 - T2940 COSM4663658 c.424G>T p.A142S Substitution - Missense 23:15252263-15252263 - TCGA-D1-A17A-01 COSM1117262 c.868T>C p.F290L Substitution - Missense 23:15244523-15244523 - TCGA-56-6545-01 COSM1151534 c.16G>C p.G6R Substitution - Missense 23:15269859-15269859 - C135 COSM4618904 c.170G>A p.S57N Substitution - Missense 23:15258870-15258870 - T23 COSM5618174 c.572C>T p.A191V Substitution - Missense 23:15248932-15248932 - HCC124T COSM1625653 c.438C>T p.H146H Substitution - coding silent 23:15250560-15250560 - 2492730 COSM5728290 c.116C>T p.P39L Substitution - Missense 23:15258924-15258924 - Pat_24_B COSM5877333 c.436C>T p.H146Y Substitution - Missense 23:15250562-15250562 - S01861 COSM5671489 c.290G>T p.G97V Substitution - Missense 23:15252397-15252397 - Pat_70_B COSM5877331 c.766C>T p.P256S Substitution - Missense 23:15244625-15244625 - PD4120a COSM159217 c.605C>T p.P202L Substitution - Missense 23:15248899-15248899 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.19404 1515664|dbSNP|BC001244|A/T|non-coding||1348|Validated; 1515664|dbSNP|BC013172|A/T|non-coding||1387|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I22S c.65T>G X 15287932 STAD A G IntronicSNV . c.761-63T>C X 15262815 NSCLC A G Missense p.F290L c.868T>C X 15262645 UCEC A G Missense p.S257P c.769T>C X 15262744 BRCA C A Missense p.G6V c.17G>T X 15287980 LUSC C A Nonsense p.E188* c.562G>T X 15268558 HNSC C A Nonsense p.E213* c.637G>T X 15266989 GBM C G Missense p.G6R c.16G>C X 15287981 LUSC C T Missense p.G198D c.593G>A X 15267033 BRCA C T Missense p.G3D c.8G>A X 15287989 UCEC C T Nonsense p.W102* c.306G>A X 15270503 UCEC G A IntronicSNV . c.95-98C>T X 15277165 CM G A Missense p.P202L c.605C>T X 15267021 BRCA G A Missense p.S83F c.248C>T X 15272893 LGG G A Synonymous p.F249F c.747C>T X 15266879 LUAD G A Synonymous p.H124H c.372C>T X 15270437 HNSC G A Synonymous p.S165S c.495C>T X 15268625 CM G C Missense p.L187V c.559C>G X 15268561 LUSC G T Missense p.P170T c.508C>A X 15268612 LUSC T A Missense p.I56F c.166A>T X 15276996 LUAD T A Missense p.R143W c.427A>T X 15270382 LUSC T C Missense p.H74R c.221A>G X 15272920 BRCA T C Missense p.Q179R c.536A>G X 15268584 LUAD