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 15 101170033 101170033 + Missense_Mutation SNP G G C TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr15:101170033G>C c.603G>C c.(601-603)caG>caC p.Q201H BRCA 15 101152633 101152636 + Splice_Site DEL GTGA GTGA - TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr15:101152633_101152636delGTGA c.e4+1 BRCA 15 101169774 101169774 + Missense_Mutation SNP A A G TCGA-AN-A0AL-01A-11W-A019-09 TCGA-AN-A0AL-10A-01W-A021-09 g.chr15:101169774A>G c.344A>G c.(343-345)aAt>aGt p.N115S BRCA 15 101188558 101188558 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:101188558G>A c.848G>A c.(847-849)cGa>cAa p.R283Q CHOL 15 101170164 101170164 + Missense_Mutation SNP A A G TCGA-3X-AAVE-01A-11D-A417-09 TCGA-3X-AAVE-10A-01D-A41A-09 g.chr15:101170164A>G c.734A>G c.(733-735)tAt>tGt p.Y245C COAD 15 101152537 101152537 + Frame_Shift_Del DEL C C - TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:101152537delC c.116delC c.(115-117)tccfs p.S39fs COAD 15 101169728 101169728 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr15:101169728A>G c.298A>G c.(298-300)Atg>Gtg p.M100V COAD 15 101169889 101169889 + Silent SNP G G A TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr15:101169889G>A c.459G>A c.(457-459)ccG>ccA p.P153P COAD 15 101170215 101170215 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr15:101170215G>A c.785G>A c.(784-786)cGa>cAa p.R262Q COADREAD 15 101152537 101152537 + Frame_Shift_Del DEL C C - TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:101152537delC c.116delC c.(115-117)tccfs p.S39fs COADREAD 15 101169728 101169728 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr15:101169728A>G c.298A>G c.(298-300)Atg>Gtg p.M100V COADREAD 15 101169889 101169889 + Silent SNP G G A TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr15:101169889G>A c.459G>A c.(457-459)ccG>ccA p.P153P COADREAD 15 101169898 101169898 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:101169898C>T c.468C>T c.(466-468)ctC>ctT p.L156L COADREAD 15 101170215 101170215 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr15:101170215G>A c.785G>A c.(784-786)cGa>cAa p.R262Q COADREAD 15 101188573 101188573 + Missense_Mutation SNP A A G TCGA-DC-6683-01A-11D-1826-10 TCGA-DC-6683-10A-01D-1826-10 g.chr15:101188573A>G c.863A>G c.(862-864)cAa>cGa p.Q288R COADREAD 15 101188654 101188654 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:101188654T>G c.944T>G c.(943-945)tTt>tGt p.F315C ESCA 15 101169730 101169730 + Missense_Mutation SNP G G A TCGA-IG-A4QS-01A-11D-A27G-09 TCGA-IG-A4QS-10A-01D-A27G-09 g.chr15:101169730G>A c.300G>A c.(298-300)atG>atA p.M100I ESCA 15 101170231 101170231 + Silent SNP C C T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr15:101170231C>T c.801C>T c.(799-801)ttC>ttT p.F267F GBMLGG 15 101170214 101170214 + Nonsense_Mutation SNP C C T TCGA-HT-8104-01A-11D-2395-08 TCGA-HT-8104-10A-01D-2396-08 g.chr15:101170214C>T c.784C>T c.(784-786)Cga>Tga p.R262* KICH 15 101170058 101170058 + Missense_Mutation SNP C C T TCGA-KO-8407-01A-11D-2310-10 TCGA-KO-8407-11A-01D-2311-10 g.chr15:101170058C>T c.628C>T c.(628-630)Cgc>Tgc p.R210C KIPAN 15 101170058 101170058 + Missense_Mutation SNP C C T TCGA-KO-8407-01A-11D-2310-10 TCGA-KO-8407-11A-01D-2311-10 g.chr15:101170058C>T c.628C>T c.(628-630)Cgc>Tgc p.R210C LGG 15 101170214 101170214 + Nonsense_Mutation SNP C C T TCGA-HT-8104-01A-11D-2395-08 TCGA-HT-8104-10A-01D-2396-08 g.chr15:101170214C>T c.784C>T c.(784-786)Cga>Tga p.R262* LIHC 15 101152549 101152549 + Missense_Mutation SNP G G A TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr15:101152549G>A c.128G>A c.(127-129)cGa>cAa p.R43Q LUAD 15 101170046 101170046 + Missense_Mutation SNP A A T TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr15:101170046A>T c.616A>T c.(616-618)Aca>Tca p.T206S LUAD 15 101170058 101170058 + Missense_Mutation SNP C C T TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr15:101170058C>T c.628C>T c.(628-630)Cgc>Tgc p.R210C LUAD 15 101170138 101170138 + Silent SNP C C T TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr15:101170138C>T c.708C>T c.(706-708)taC>taT p.Y236Y LUSC 15 101169888 101169888 + Missense_Mutation SNP C C T TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr15:101169888C>T c.458C>T c.(457-459)cCg>cTg p.P153L LUSC 15 101169983 101169983 + Nonsense_Mutation SNP C C T TCGA-34-5232-01A-21D-1817-08 TCGA-34-5232-10A-01D-1817-08 g.chr15:101169983C>T c.553C>T c.(553-555)Cga>Tga p.R185* LUSC 15 101188614 101188614 + Missense_Mutation SNP C C G TCGA-66-2781-01A-01D-1522-08 TCGA-66-2781-11A-01D-1522-08 g.chr15:101188614C>G c.904C>G c.(904-906)Cca>Gca p.P302A PRAD 15 101169708 101169708 + Missense_Mutation SNP G G A TCGA-HC-7232-01A-11D-2114-08 TCGA-HC-7232-10A-01D-2115-08 g.chr15:101169708G>A c.278G>A c.(277-279)cGg>cAg p.R93Q READ 15 101169898 101169898 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:101169898C>T c.468C>T c.(466-468)ctC>ctT p.L156L READ 15 101188573 101188573 + Missense_Mutation SNP A A G TCGA-DC-6683-01A-11D-1826-10 TCGA-DC-6683-10A-01D-1826-10 g.chr15:101188573A>G c.863A>G c.(862-864)cAa>cGa p.Q288R READ 15 101188654 101188654 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr15:101188654T>G c.944T>G c.(943-945)tTt>tGt p.F315C SKCM 15 101188569 101188569 + Nonsense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:101188569C>T c.859C>T c.(859-861)Cga>Tga p.R287*

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 15 101181321 101181321 single base substitution G T intron_variant BRCA-EU 15 101142789 101142789 single base substitution A G 5_prime_UTR_variant BRCA-EU 15 101142789 101142789 single base substitution A G upstream_gene_variant BRCA-EU 15 101144391 101144391 single base substitution G C intron_variant BRCA-EU 15 101145120 101145120 single base substitution G A intron_variant BRCA-EU 15 101145120 101145120 single base substitution G A upstream_gene_variant BRCA-EU 15 101148070 101148070 single base substitution T G intron_variant BRCA-EU 15 101148070 101148070 single base substitution T G upstream_gene_variant BRCA-EU 15 101149608 101149608 single base substitution G A intron_variant BRCA-EU 15 101149608 101149608 single base substitution G A upstream_gene_variant BRCA-EU 15 101149774 101149774 single base substitution G C exon_variant BRCA-EU 15 101149774 101149774 single base substitution G C intron_variant BRCA-EU 15 101150171 101150171 single base substitution T C intron_variant BRCA-EU 15 101151268 101151268 single base substitution G C intron_variant BRCA-EU 15 101151538 101151538 single base substitution C A intron_variant BRCA-EU 15 101152070 101152070 single base substitution G A intron_variant BRCA-EU 15 101152565 101152565 single base substitution G A exon_variant BRCA-EU 15 101152565 101152565 single base substitution G A stop_gained W48* 144G>A BRCA-EU 15 101153239 101153239 single base substitution T C downstream_gene_variant BRCA-EU 15 101153239 101153239 single base substitution T C intron_variant BRCA-EU 15 101153549 101153549 single base substitution A G downstream_gene_variant BRCA-EU 15 101153549 101153549 single base substitution A G intron_variant BRCA-EU 15 101154237 101154237 single base substitution G T downstream_gene_variant BRCA-EU 15 101154237 101154237 single base substitution G T intron_variant BRCA-EU 15 101154283 101154283 single base substitution G A downstream_gene_variant BRCA-EU 15 101154283 101154283 single base substitution G A intron_variant BRCA-EU 15 101155940 101155940 single base substitution C G downstream_gene_variant BRCA-EU 15 101155940 101155940 single base substitution C G intron_variant BRCA-EU 15 101156413 101156413 single base substitution A G downstream_gene_variant BRCA-EU 15 101156413 101156413 single base substitution A G intron_variant BRCA-EU 15 101157986 101157986 single base substitution G C intron_variant BRCA-EU 15 101158319 101158319 single base substitution T A intron_variant BRCA-EU 15 101159979 101159979 single base substitution G C intron_variant BRCA-EU 15 101163865 101163865 single base substitution G T intron_variant BRCA-EU 15 101163869 101163869 deletion of <=200bp A - intron_variant BRCA-EU 15 101165012 101165012 single base substitution C T intron_variant BRCA-EU 15 101165849 101165849 single base substitution G C intron_variant BRCA-EU 15 101166209 101166209 single base substitution T A intron_variant BRCA-EU 15 101166883 101166883 single base substitution T C intron_variant BRCA-EU 15 101172069 101172069 single base substitution A G downstream_gene_variant BRCA-EU 15 101172069 101172069 single base substitution A G intron_variant BRCA-EU 15 101172243 101172243 single base substitution G A downstream_gene_variant BRCA-EU 15 101172243 101172243 single base substitution G A intron_variant BRCA-EU 15 101172253 101172253 single base substitution G T downstream_gene_variant BRCA-EU 15 101172253 101172253 single base substitution G T intron_variant BRCA-EU 15 101174228 101174228 single base substitution G A downstream_gene_variant BRCA-EU 15 101174228 101174228 single base substitution G A intron_variant BRCA-EU 15 101175737 101175737 single base substitution G T intron_variant BRCA-EU 15 101176384 101176384 single base substitution C G intron_variant BRCA-EU 15 101176483 101176483 single base substitution G C intron_variant BRCA-EU 15 101177044 101177044 single base substitution G A intron_variant BRCA-EU 15 101177283 101177283 single base substitution C T intron_variant BRCA-EU 15 101178832 101178832 single base substitution T C intron_variant BRCA-EU 15 101179161 101179161 single base substitution C T intron_variant BRCA-EU 15 101180413 101180413 single base substitution G C intron_variant BRCA-EU 15 101182083 101182083 single base substitution G C intron_variant BRCA-EU 15 101186275 101186275 single base substitution T A intron_variant BRCA-EU 15 101187115 101187115 single base substitution G C intron_variant BRCA-EU 15 101187549 101187549 single base substitution C G intron_variant BRCA-EU 15 101187657 101187657 single base substitution A G intron_variant BRCA-EU 15 101188503 101188503 single base substitution C T intron_variant BRCA-EU 15 101188752 101188752 single base substitution A T 3_prime_UTR_variant BRCA-EU 15 101191260 101191260 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 101191260 101191260 single base substitution G A downstream_gene_variant BRCA-EU 15 101193084 101193084 single base substitution G C downstream_gene_variant BRCA-EU 15 101193951 101193951 single base substitution G T downstream_gene_variant BRCA-EU 15 101195102 101195102 single base substitution C T downstream_gene_variant BRCA-EU 15 101195583 101195583 single base substitution C G downstream_gene_variant BRCA-EU 15 101195939 101195939 single base substitution G A downstream_gene_variant BRCA-EU 15 101196699 101196699 single base substitution C T downstream_gene_variant BRCA-EU 15 101196844 101196844 single base substitution G T downstream_gene_variant BRCA-FR 15 101152565 101152565 single base substitution G A exon_variant BRCA-FR 15 101152565 101152565 single base substitution G A stop_gained W48* 144G>A BRCA-FR 15 101155940 101155940 single base substitution C G downstream_gene_variant BRCA-FR 15 101155940 101155940 single base substitution C G intron_variant BRCA-FR 15 101157986 101157986 single base substitution G C intron_variant BRCA-FR 15 101164691 101164691 single base substitution G A intron_variant BRCA-FR 15 101170819 101170819 single base substitution A G downstream_gene_variant BRCA-FR 15 101170819 101170819 single base substitution A G intron_variant BRCA-FR 15 101176483 101176483 single base substitution G C intron_variant BRCA-FR 15 101182083 101182083 single base substitution G C intron_variant BRCA-FR 15 101183131 101183131 single base substitution G T intron_variant BRCA-FR 15 101193084 101193084 single base substitution G C downstream_gene_variant BRCA-FR 15 101196699 101196699 single base substitution C T downstream_gene_variant BRCA-UK 15 101169856 101169856 single base substitution G A intron_variant BRCA-UK 15 101169856 101169856 single base substitution G A synonymous_variant E142E 426G>A BRCA-US 15 101152633 101152636 deletion of <=200bp GTGA - exon_variant BRCA-US 15 101152633 101152636 deletion of <=200bp GTGA - splice_donor_variant BRCA-US 15 101169774 101169774 single base substitution A G intron_variant BRCA-US 15 101169774 101169774 single base substitution A G missense_variant N115S 344A>G BRCA-US 15 101188558 101188558 single base substitution G A missense_variant R283Q 848G>A BRCA-US 15 101188558 101188558 single base substitution G A missense_variant R81Q 242G>A CLLE-ES 15 101151175 101151175 single base substitution C T intron_variant CLLE-ES 15 101159823 101159823 single base substitution A C intron_variant CLLE-ES 15 101177461 101177461 single base substitution C T intron_variant CLLE-ES 15 101181243 101181243 single base substitution G C intron_variant CLLE-ES 15 101191955 101191955 single base substitution G A downstream_gene_variant COAD-US 15 101152537 101152537 deletion of <=200bp C - exon_variant COAD-US 15 101152537 101152537 deletion of <=200bp C - frameshift_variant S39 COAD-US 15 101169722 101169722 single base substitution C T intron_variant COAD-US 15 101169722 101169722 single base substitution C T missense_variant R98C 292C>T COAD-US 15 101169889 101169889 single base substitution G A intron_variant COAD-US 15 101169889 101169889 single base substitution G A synonymous_variant P153P 459G>A COAD-US 15 101170215 101170215 single base substitution G A intron_variant COAD-US 15 101170215 101170215 single base substitution G A missense_variant R262Q 785G>A COCA-CN 15 101171527 101171527 single base substitution C T downstream_gene_variant COCA-CN 15 101171527 101171527 single base substitution C T intron_variant ESAD-UK 15 101138735 101138735 single base substitution G A upstream_gene_variant ESAD-UK 15 101139803 101139803 single base substitution T C upstream_gene_variant ESAD-UK 15 101141545 101141545 single base substitution T C upstream_gene_variant ESAD-UK 15 101142362 101142362 single base substitution C T upstream_gene_variant ESAD-UK 15 101143712 101143712 single base substitution A T intron_variant ESAD-UK 15 101145923 101145923 single base substitution G A intron_variant ESAD-UK 15 101145923 101145923 single base substitution G A upstream_gene_variant ESAD-UK 15 101148591 101148591 single base substitution G T intron_variant ESAD-UK 15 101148591 101148591 single base substitution G T upstream_gene_variant ESAD-UK 15 101149949 101149949 single base substitution T G 5_prime_UTR_variant ESAD-UK 15 101149949 101149949 single base substitution T G exon_variant ESAD-UK 15 101154326 101154326 single base substitution A T downstream_gene_variant ESAD-UK 15 101154326 101154326 single base substitution A T intron_variant ESAD-UK 15 101157102 101157102 single base substitution T C downstream_gene_variant ESAD-UK 15 101157102 101157102 single base substitution T C intron_variant ESAD-UK 15 101161261 101161261 single base substitution G A intron_variant ESAD-UK 15 101162068 101162068 single base substitution A G intron_variant ESAD-UK 15 101164148 101164148 single base substitution G A intron_variant ESAD-UK 15 101164482 101164482 single base substitution A G intron_variant ESAD-UK 15 101166168 101166168 single base substitution G A intron_variant ESAD-UK 15 101167493 101167493 single base substitution G A intron_variant ESAD-UK 15 101167991 101167991 single base substitution A T intron_variant ESAD-UK 15 101168204 101168204 single base substitution A C intron_variant ESAD-UK 15 101172134 101172134 single base substitution A T downstream_gene_variant ESAD-UK 15 101172134 101172134 single base substitution A T intron_variant ESAD-UK 15 101173068 101173068 single base substitution A C downstream_gene_variant ESAD-UK 15 101173068 101173068 single base substitution A C intron_variant ESAD-UK 15 101175504 101175504 single base substitution C T intron_variant ESAD-UK 15 101177354 101177354 single base substitution G A intron_variant ESAD-UK 15 101178222 101178222 single base substitution G T intron_variant ESAD-UK 15 101179134 101179134 single base substitution A G intron_variant ESAD-UK 15 101181568 101181568 deletion of <=200bp A - intron_variant ESAD-UK 15 101184674 101184674 single base substitution C A intron_variant ESAD-UK 15 101185419 101185419 single base substitution A G intron_variant ESAD-UK 15 101190010 101190010 single base substitution C A 3_prime_UTR_variant ESAD-UK 15 101190010 101190010 single base substitution C A downstream_gene_variant ESAD-UK 15 101190904 101190904 single base substitution T A 3_prime_UTR_variant ESAD-UK 15 101190904 101190904 single base substitution T A downstream_gene_variant ESAD-UK 15 101192704 101192704 single base substitution G C downstream_gene_variant ESAD-UK 15 101193944 101193944 single base substitution T A downstream_gene_variant ESAD-UK 15 101194960 101194960 single base substitution T C downstream_gene_variant ESCA-CN 15 101152512 101152512 single base substitution C T exon_variant ESCA-CN 15 101152512 101152512 single base substitution C T stop_gained R31* 91C>T ESCA-CN 15 101170058 101170058 single base substitution C T intron_variant ESCA-CN 15 101170058 101170058 single base substitution C T missense_variant R210C 628C>T KIRP-US 15 101152488 101152488 single base substitution G A exon_variant KIRP-US 15 101152488 101152488 single base substitution G A missense_variant A23T 67G>A LGG-US 15 101170214 101170214 single base substitution C T intron_variant LGG-US 15 101170214 101170214 single base substitution C T stop_gained R262* 784C>T LICA-FR 15 101142455 101142455 single base substitution G C upstream_gene_variant LICA-FR 15 101146445 101146445 single base substitution A G intron_variant LICA-FR 15 101146445 101146445 single base substitution A G upstream_gene_variant LICA-FR 15 101173859 101173859 single base substitution G T downstream_gene_variant LICA-FR 15 101173859 101173859 single base substitution G T intron_variant LICA-FR 15 101182160 101182160 single base substitution G A intron_variant LICA-FR 15 101184901 101184901 single base substitution T C intron_variant LICA-FR 15 101185681 101185681 single base substitution G A intron_variant LINC-JP 15 101142415 101142415 single base substitution C A upstream_gene_variant LINC-JP 15 101160759 101160759 single base substitution T C intron_variant LINC-JP 15 101172322 101172322 single base substitution G C downstream_gene_variant LINC-JP 15 101172322 101172322 single base substitution G C intron_variant LINC-JP 15 101175344 101175344 single base substitution G A downstream_gene_variant LINC-JP 15 101175344 101175344 single base substitution G A intron_variant LINC-JP 15 101186445 101186445 single base substitution A C intron_variant LINC-JP 15 101191403 101191403 deletion of <=200bp T - 3_prime_UTR_variant LINC-JP 15 101191403 101191403 deletion of <=200bp T - downstream_gene_variant LIRI-JP 15 101138038 101138038 single base substitution C T upstream_gene_variant LIRI-JP 15 101139770 101139770 single base substitution C T upstream_gene_variant LIRI-JP 15 101140907 101140907 single base substitution T C upstream_gene_variant LIRI-JP 15 101144222 101144222 single base substitution T G intron_variant LIRI-JP 15 101146837 101146837 single base substitution G A intron_variant LIRI-JP 15 101146837 101146837 single base substitution G A upstream_gene_variant LIRI-JP 15 101149307 101149307 single base substitution A T intron_variant LIRI-JP 15 101149307 101149307 single base substitution A T upstream_gene_variant LIRI-JP 15 101150128 101150128 single base substitution A G intron_variant LIRI-JP 15 101154405 101154405 single base substitution G T downstream_gene_variant LIRI-JP 15 101154405 101154405 single base substitution G T intron_variant LIRI-JP 15 101154763 101154763 single base substitution T C downstream_gene_variant LIRI-JP 15 101154763 101154763 single base substitution T C intron_variant LIRI-JP 15 101155109 101155109 single base substitution A G downstream_gene_variant LIRI-JP 15 101155109 101155109 single base substitution A G intron_variant LIRI-JP 15 101155238 101155238 single base substitution C T downstream_gene_variant LIRI-JP 15 101155238 101155238 single base substitution C T intron_variant LIRI-JP 15 101155472 101155472 single base substitution T C downstream_gene_variant LIRI-JP 15 101155472 101155472 single base substitution T C intron_variant LIRI-JP 15 101158980 101158980 single base substitution C T intron_variant LIRI-JP 15 101159730 101159730 single base substitution G T intron_variant LIRI-JP 15 101162099 101162099 single base substitution C T intron_variant LIRI-JP 15 101162793 101162793 single base substitution G T intron_variant LIRI-JP 15 101162865 101162865 single base substitution A G intron_variant LIRI-JP 15 101165801 101165801 single base substitution A G intron_variant LIRI-JP 15 101167131 101167131 single base substitution A T intron_variant LIRI-JP 15 101168875 101168875 deletion of <=200bp T - intron_variant LIRI-JP 15 101168938 101168938 single base substitution G A intron_variant LIRI-JP 15 101177193 101177193 single base substitution G A intron_variant LIRI-JP 15 101178572 101178572 single base substitution A T intron_variant LIRI-JP 15 101185482 101185482 single base substitution A G intron_variant LIRI-JP 15 101191588 101191588 single base substitution A G 3_prime_UTR_variant LIRI-JP 15 101191588 101191588 single base substitution A G downstream_gene_variant LIRI-JP 15 101193153 101193153 single base substitution A G downstream_gene_variant LIRI-JP 15 101196467 101196467 single base substitution G A downstream_gene_variant LUSC-KR 15 101143243 101143243 single base substitution A T 5_prime_UTR_variant LUSC-KR 15 101148414 101148414 single base substitution A G intron_variant LUSC-KR 15 101148414 101148414 single base substitution A G upstream_gene_variant LUSC-KR 15 101153234 101153234 single base substitution G T downstream_gene_variant LUSC-KR 15 101153234 101153234 single base substitution G T intron_variant LUSC-KR 15 101168639 101168639 single base substitution C G intron_variant LUSC-KR 15 101173558 101173558 single base substitution G A downstream_gene_variant LUSC-KR 15 101173558 101173558 single base substitution G A intron_variant LUSC-KR 15 101176504 101176504 single base substitution C G intron_variant LUSC-KR 15 101180650 101180650 single base substitution T A intron_variant LUSC-KR 15 101181940 101181940 single base substitution G T intron_variant LUSC-KR 15 101181941 101181941 single base substitution A T intron_variant LUSC-KR 15 101185115 101185115 single base substitution G T intron_variant LUSC-KR 15 101186310 101186310 single base substitution G A intron_variant LUSC-KR 15 101186633 101186633 single base substitution G T intron_variant LUSC-KR 15 101186834 101186834 single base substitution G T intron_variant LUSC-KR 15 101186917 101186917 single base substitution G A intron_variant LUSC-KR 15 101187210 101187210 single base substitution T C intron_variant LUSC-KR 15 101191829 101191829 single base substitution A G 3_prime_UTR_variant LUSC-KR 15 101191829 101191829 single base substitution A G downstream_gene_variant LUSC-US 15 101169888 101169888 single base substitution C T intron_variant LUSC-US 15 101169888 101169888 single base substitution C T missense_variant P153L 458C>T LUSC-US 15 101169983 101169983 single base substitution C T intron_variant LUSC-US 15 101169983 101169983 single base substitution C T stop_gained R185* 553C>T LUSC-US 15 101188614 101188614 single base substitution C G missense_variant P100A 298C>G LUSC-US 15 101188614 101188614 single base substitution C G missense_variant P302A 904C>G MALY-DE 15 101141762 101141765 deletion of <=200bp CTAT - upstream_gene_variant MALY-DE 15 101143907 101143907 single base substitution C G intron_variant MALY-DE 15 101156774 101156774 single base substitution T G downstream_gene_variant MALY-DE 15 101156774 101156774 single base substitution T G intron_variant MALY-DE 15 101168177 101168177 single base substitution C T intron_variant MALY-DE 15 101174715 101174715 single base substitution G A downstream_gene_variant MALY-DE 15 101174715 101174715 single base substitution G A intron_variant MALY-DE 15 101175328 101175328 deletion of <=200bp G - downstream_gene_variant MALY-DE 15 101175328 101175328 deletion of <=200bp G - intron_variant MALY-DE 15 101194618 101194618 single base substitution C T downstream_gene_variant MELA-AU 15 101137826 101137826 single base substitution C A upstream_gene_variant MELA-AU 15 101138255 101138255 single base substitution C A upstream_gene_variant MELA-AU 15 101138370 101138370 single base substitution G A upstream_gene_variant MELA-AU 15 101139321 101139321 single base substitution G A upstream_gene_variant MELA-AU 15 101139663 101139663 single base substitution G A upstream_gene_variant MELA-AU 15 101141991 101141991 single base substitution A G upstream_gene_variant MELA-AU 15 101142224 101142224 single base substitution G A upstream_gene_variant MELA-AU 15 101142445 101142445 single base substitution G A upstream_gene_variant MELA-AU 15 101142613 101142613 single base substitution G A upstream_gene_variant MELA-AU 15 101142700 101142700 single base substitution C T upstream_gene_variant MELA-AU 15 101143260 101143260 single base substitution C T intron_variant MELA-AU 15 101143376 101143376 single base substitution C T intron_variant MELA-AU 15 101143859 101143860 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 101144551 101144551 single base substitution C T intron_variant MELA-AU 15 101145519 101145519 single base substitution T C intron_variant MELA-AU 15 101145519 101145519 single base substitution T C upstream_gene_variant MELA-AU 15 101145566 101145566 single base substitution C T intron_variant MELA-AU 15 101145566 101145566 single base substitution C T upstream_gene_variant MELA-AU 15 101145772 101145772 single base substitution G A intron_variant MELA-AU 15 101145772 101145772 single base substitution G A upstream_gene_variant MELA-AU 15 101146319 101146319 single base substitution C T intron_variant MELA-AU 15 101146319 101146319 single base substitution C T upstream_gene_variant MELA-AU 15 101148972 101148972 single base substitution C T intron_variant MELA-AU 15 101148972 101148972 single base substitution C T upstream_gene_variant MELA-AU 15 101150000 101150000 single base substitution C T 5_prime_UTR_variant MELA-AU 15 101150000 101150000 single base substitution C T exon_variant MELA-AU 15 101150008 101150008 single base substitution C T 5_prime_UTR_variant MELA-AU 15 101150008 101150008 single base substitution C T exon_variant MELA-AU 15 101150305 101150305 single base substitution C T intron_variant MELA-AU 15 101150372 101150372 single base substitution C T intron_variant MELA-AU 15 101151200 101151200 single base substitution C T intron_variant MELA-AU 15 101152613 101152613 single base substitution G A exon_variant MELA-AU 15 101152613 101152613 single base substitution G A synonymous_variant R64R 192G>A MELA-AU 15 101152833 101152833 single base substitution T A downstream_gene_variant MELA-AU 15 101152833 101152833 single base substitution T A intron_variant MELA-AU 15 101152886 101152886 single base substitution C T downstream_gene_variant MELA-AU 15 101152886 101152886 single base substitution C T intron_variant MELA-AU 15 101153055 101153055 single base substitution C T downstream_gene_variant MELA-AU 15 101153055 101153055 single base substitution C T intron_variant MELA-AU 15 101153145 101153145 single base substitution G A downstream_gene_variant MELA-AU 15 101153145 101153145 single base substitution G A intron_variant MELA-AU 15 101153310 101153310 single base substitution C T downstream_gene_variant MELA-AU 15 101153310 101153310 single base substitution C T intron_variant MELA-AU 15 101153974 101153974 single base substitution A C downstream_gene_variant MELA-AU 15 101153974 101153974 single base substitution A C intron_variant MELA-AU 15 101154472 101154472 single base substitution C T downstream_gene_variant MELA-AU 15 101154472 101154472 single base substitution C T intron_variant MELA-AU 15 101156582 101156582 single base substitution T C downstream_gene_variant MELA-AU 15 101156582 101156582 single base substitution T C intron_variant MELA-AU 15 101156617 101156617 single base substitution T C downstream_gene_variant MELA-AU 15 101156617 101156617 single base substitution T C intron_variant MELA-AU 15 101156863 101156863 single base substitution T A downstream_gene_variant MELA-AU 15 101156863 101156863 single base substitution T A intron_variant MELA-AU 15 101157327 101157327 single base substitution C T downstream_gene_variant MELA-AU 15 101157327 101157327 single base substitution C T intron_variant MELA-AU 15 101157348 101157348 single base substitution T G downstream_gene_variant MELA-AU 15 101157348 101157348 single base substitution T G intron_variant MELA-AU 15 101157432 101157432 single base substitution C T downstream_gene_variant MELA-AU 15 101157432 101157432 single base substitution C T intron_variant MELA-AU 15 101157497 101157497 single base substitution C T downstream_gene_variant MELA-AU 15 101157497 101157497 single base substitution C T intron_variant MELA-AU 15 101157731 101157731 single base substitution C T intron_variant MELA-AU 15 101158208 101158208 single base substitution G A intron_variant MELA-AU 15 101158267 101158267 single base substitution C T intron_variant MELA-AU 15 101160105 101160105 single base substitution C T intron_variant MELA-AU 15 101160540 101160540 single base substitution C T intron_variant MELA-AU 15 101160947 101160947 single base substitution C T intron_variant MELA-AU 15 101162068 101162068 single base substitution A G intron_variant MELA-AU 15 101162643 101162643 single base substitution C T intron_variant MELA-AU 15 101162749 101162750 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 101162908 101162908 single base substitution C T intron_variant MELA-AU 15 101164277 101164277 single base substitution C T intron_variant MELA-AU 15 101165049 101165049 single base substitution C T intron_variant MELA-AU 15 101165341 101165341 single base substitution G A intron_variant MELA-AU 15 101165360 101165360 single base substitution C T intron_variant MELA-AU 15 101165780 101165780 single base substitution C T intron_variant MELA-AU 15 101167308 101167308 single base substitution C T intron_variant MELA-AU 15 101167340 101167340 single base substitution C T intron_variant MELA-AU 15 101168224 101168224 single base substitution C T intron_variant MELA-AU 15 101168373 101168373 single base substitution T A intron_variant MELA-AU 15 101169029 101169029 single base substitution C T intron_variant MELA-AU 15 101169034 101169034 single base substitution A G intron_variant MELA-AU 15 101169901 101169901 single base substitution C T intron_variant MELA-AU 15 101169901 101169901 single base substitution C T synonymous_variant A157A 471C>T MELA-AU 15 101170177 101170177 single base substitution C T intron_variant MELA-AU 15 101170177 101170177 single base substitution C T synonymous_variant T249T 747C>T MELA-AU 15 101170433 101170433 single base substitution A T downstream_gene_variant MELA-AU 15 101170433 101170433 single base substitution A T intron_variant MELA-AU 15 101170436 101170436 single base substitution C T downstream_gene_variant MELA-AU 15 101170436 101170436 single base substitution C T intron_variant MELA-AU 15 101170638 101170638 single base substitution C T downstream_gene_variant MELA-AU 15 101170638 101170638 single base substitution C T intron_variant MELA-AU 15 101170639 101170639 single base substitution C T downstream_gene_variant MELA-AU 15 101170639 101170639 single base substitution C T intron_variant MELA-AU 15 101170836 101170837 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 101170836 101170837 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 101170840 101170841 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 101170840 101170841 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 101171107 101171107 single base substitution T A downstream_gene_variant MELA-AU 15 101171107 101171107 single base substitution T A intron_variant MELA-AU 15 101172719 101172719 single base substitution G A downstream_gene_variant MELA-AU 15 101172719 101172719 single base substitution G A intron_variant MELA-AU 15 101173067 101173067 single base substitution A C downstream_gene_variant MELA-AU 15 101173067 101173067 single base substitution A C intron_variant MELA-AU 15 101174120 101174120 single base substitution C T downstream_gene_variant MELA-AU 15 101174120 101174120 single base substitution C T intron_variant MELA-AU 15 101174497 101174497 single base substitution G A downstream_gene_variant MELA-AU 15 101174497 101174497 single base substitution G A intron_variant MELA-AU 15 101174837 101174837 single base substitution C A downstream_gene_variant MELA-AU 15 101174837 101174837 single base substitution C A intron_variant MELA-AU 15 101175226 101175226 single base substitution C T downstream_gene_variant MELA-AU 15 101175226 101175226 single base substitution C T intron_variant MELA-AU 15 101175360 101175360 single base substitution T G downstream_gene_variant MELA-AU 15 101175360 101175360 single base substitution T G intron_variant MELA-AU 15 101176189 101176189 single base substitution C T intron_variant MELA-AU 15 101176194 101176194 single base substitution C T intron_variant MELA-AU 15 101176219 101176219 single base substitution G A intron_variant MELA-AU 15 101177055 101177055 single base substitution G A intron_variant MELA-AU 15 101177075 101177075 single base substitution G A intron_variant MELA-AU 15 101177164 101177164 single base substitution C T intron_variant MELA-AU 15 101177968 101177968 single base substitution C T intron_variant MELA-AU 15 101178219 101178219 single base substitution A G intron_variant MELA-AU 15 101178773 101178773 single base substitution C T intron_variant MELA-AU 15 101179068 101179068 single base substitution C T intron_variant MELA-AU 15 101179347 101179347 single base substitution T C intron_variant MELA-AU 15 101179444 101179444 single base substitution T C intron_variant MELA-AU 15 101179723 101179723 single base substitution C T intron_variant MELA-AU 15 101179833 101179833 single base substitution T G intron_variant MELA-AU 15 101180284 101180284 single base substitution C T intron_variant MELA-AU 15 101180809 101180809 single base substitution C T intron_variant MELA-AU 15 101181392 101181392 single base substitution C G intron_variant MELA-AU 15 101182757 101182757 single base substitution C T intron_variant MELA-AU 15 101182830 101182830 single base substitution T A intron_variant MELA-AU 15 101183255 101183256 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 15 101183518 101183518 single base substitution G A intron_variant MELA-AU 15 101183914 101183914 single base substitution G A intron_variant MELA-AU 15 101184953 101184953 single base substitution C T intron_variant MELA-AU 15 101185093 101185093 single base substitution C T intron_variant MELA-AU 15 101187429 101187429 single base substitution G A intron_variant MELA-AU 15 101187672 101187672 single base substitution C T intron_variant MELA-AU 15 101187752 101187752 single base substitution C T intron_variant MELA-AU 15 101189188 101189188 single base substitution T A 3_prime_UTR_variant MELA-AU 15 101189977 101189977 single base substitution C T 3_prime_UTR_variant MELA-AU 15 101189977 101189977 single base substitution C T downstream_gene_variant MELA-AU 15 101190031 101190031 single base substitution C T 3_prime_UTR_variant MELA-AU 15 101190031 101190031 single base substitution C T downstream_gene_variant MELA-AU 15 101191730 101191730 single base substitution C T 3_prime_UTR_variant MELA-AU 15 101191730 101191730 single base substitution C T downstream_gene_variant MELA-AU 15 101192162 101192162 single base substitution C T downstream_gene_variant MELA-AU 15 101192913 101192914 multiple base substitution (>=2bp and <=200bp) TT GG downstream_gene_variant MELA-AU 15 101192948 101192948 single base substitution C T downstream_gene_variant MELA-AU 15 101193777 101193777 single base substitution A G downstream_gene_variant MELA-AU 15 101193794 101193794 single base substitution C T downstream_gene_variant MELA-AU 15 101194892 101194892 single base substitution C T downstream_gene_variant MELA-AU 15 101194973 101194973 single base substitution C T downstream_gene_variant MELA-AU 15 101195008 101195008 single base substitution C T downstream_gene_variant MELA-AU 15 101195081 101195081 single base substitution C T downstream_gene_variant MELA-AU 15 101195240 101195240 single base substitution C T downstream_gene_variant MELA-AU 15 101196384 101196384 single base substitution G A downstream_gene_variant MELA-AU 15 101196403 101196403 single base substitution C T downstream_gene_variant ORCA-IN 15 101156749 101156749 single base substitution C G downstream_gene_variant ORCA-IN 15 101156749 101156749 single base substitution C G intron_variant ORCA-IN 15 101157909 101157909 single base substitution C G intron_variant ORCA-IN 15 101187795 101187795 single base substitution G A intron_variant ORCA-IN 15 101195088 101195088 single base substitution G A downstream_gene_variant OV-AU 15 101142359 101142359 single base substitution C T upstream_gene_variant OV-AU 15 101145604 101145604 single base substitution G A intron_variant OV-AU 15 101145604 101145604 single base substitution G A upstream_gene_variant OV-AU 15 101153848 101153848 single base substitution G T downstream_gene_variant OV-AU 15 101153848 101153848 single base substitution G T intron_variant OV-AU 15 101154669 101154669 single base substitution C T downstream_gene_variant OV-AU 15 101154669 101154669 single base substitution C T intron_variant OV-AU 15 101158622 101158622 single base substitution G A intron_variant OV-AU 15 101161800 101161800 single base substitution T G intron_variant OV-AU 15 101169086 101169086 single base substitution G C intron_variant OV-AU 15 101169872 101169872 single base substitution G A intron_variant OV-AU 15 101169872 101169872 single base substitution G A missense_variant D148N 442G>A OV-AU 15 101172153 101172153 single base substitution C T downstream_gene_variant OV-AU 15 101172153 101172153 single base substitution C T intron_variant OV-AU 15 101172479 101172479 single base substitution G A downstream_gene_variant OV-AU 15 101172479 101172479 single base substitution G A intron_variant OV-AU 15 101195181 101195181 single base substitution T A downstream_gene_variant PACA-AU 15 101143085 101143085 single base substitution T C 5_prime_UTR_variant PACA-AU 15 101145429 101145429 single base substitution C G intron_variant PACA-AU 15 101145429 101145429 single base substitution C G upstream_gene_variant PACA-AU 15 101149114 101149114 single base substitution G A intron_variant PACA-AU 15 101149114 101149114 single base substitution G A upstream_gene_variant PACA-AU 15 101150560 101150560 single base substitution C T intron_variant PACA-AU 15 101152750 101152753 deletion of <=200bp TCTC - downstream_gene_variant PACA-AU 15 101152750 101152753 deletion of <=200bp TCTC - intron_variant PACA-AU 15 101162252 101162252 single base substitution C A intron_variant PACA-AU 15 101164863 101164863 single base substitution T A intron_variant PACA-AU 15 101165361 101165361 single base substitution C A intron_variant PACA-AU 15 101165996 101165996 single base substitution C T intron_variant PACA-AU 15 101166145 101166145 single base substitution G C intron_variant PACA-AU 15 101168390 101168390 single base substitution A T intron_variant PACA-AU 15 101171093 101171093 single base substitution T C downstream_gene_variant PACA-AU 15 101171093 101171093 single base substitution T C intron_variant PACA-AU 15 101177174 101177174 single base substitution G T intron_variant PACA-AU 15 101177975 101177975 single base substitution G A intron_variant PACA-AU 15 101180889 101180889 single base substitution A C intron_variant PACA-AU 15 101189383 101189383 single base substitution C T 3_prime_UTR_variant PACA-AU 15 101192384 101192384 single base substitution G A downstream_gene_variant PACA-AU 15 101192935 101192937 deletion of <=200bp AAG - downstream_gene_variant PACA-AU 15 101194131 101194131 insertion of <=200bp - A downstream_gene_variant PACA-CA 15 101139683 101139683 single base substitution T C upstream_gene_variant PACA-CA 15 101139763 101139763 single base substitution C T upstream_gene_variant PACA-CA 15 101140070 101140070 single base substitution A T upstream_gene_variant PACA-CA 15 101144883 101144883 single base substitution G C intron_variant PACA-CA 15 101144883 101144883 single base substitution G C upstream_gene_variant PACA-CA 15 101151766 101151766 single base substitution C A intron_variant PACA-CA 15 101154769 101154769 single base substitution T A downstream_gene_variant PACA-CA 15 101154769 101154769 single base substitution T A intron_variant PACA-CA 15 101155710 101155711 deletion of <=200bp TT - downstream_gene_variant PACA-CA 15 101155710 101155711 deletion of <=200bp TT - intron_variant PACA-CA 15 101158965 101158965 single base substitution G T intron_variant PACA-CA 15 101159752 101159752 single base substitution A C intron_variant PACA-CA 15 101160054 101160054 single base substitution C T intron_variant PACA-CA 15 101160198 101160198 single base substitution A T intron_variant PACA-CA 15 101161527 101161527 single base substitution G A intron_variant PACA-CA 15 101163557 101163557 single base substitution G A intron_variant PACA-CA 15 101168730 101168730 single base substitution G T intron_variant PACA-CA 15 101174001 101174001 single base substitution G T downstream_gene_variant PACA-CA 15 101174001 101174001 single base substitution G T intron_variant PACA-CA 15 101191049 101191049 single base substitution A G 3_prime_UTR_variant PACA-CA 15 101191049 101191049 single base substitution A G downstream_gene_variant PACA-CA 15 101192646 101192646 single base substitution C T downstream_gene_variant PACA-CA 15 101194489 101194489 single base substitution A G downstream_gene_variant PAEN-AU 15 101145500 101145500 single base substitution A G intron_variant PAEN-AU 15 101145500 101145500 single base substitution A G upstream_gene_variant PAEN-AU 15 101157382 101157382 single base substitution A T downstream_gene_variant PAEN-AU 15 101157382 101157382 single base substitution A T intron_variant PAEN-AU 15 101166662 101166662 single base substitution G T intron_variant PAEN-AU 15 101180596 101180596 single base substitution C A intron_variant PAEN-AU 15 101186289 101186289 single base substitution A G intron_variant PAEN-IT 15 101154043 101154043 single base substitution A G downstream_gene_variant PAEN-IT 15 101154043 101154043 single base substitution A G intron_variant PAEN-IT 15 101185984 101185984 single base substitution A G intron_variant PBCA-DE 15 101139814 101139814 single base substitution C T upstream_gene_variant PBCA-DE 15 101145536 101145536 single base substitution C A intron_variant PBCA-DE 15 101145536 101145536 single base substitution C A upstream_gene_variant PBCA-DE 15 101147216 101147216 single base substitution G T intron_variant PBCA-DE 15 101147216 101147216 single base substitution G T upstream_gene_variant PBCA-DE 15 101173067 101173067 single base substitution A C downstream_gene_variant PBCA-DE 15 101173067 101173067 single base substitution A C intron_variant PBCA-DE 15 101173953 101173953 single base substitution C T downstream_gene_variant PBCA-DE 15 101173953 101173953 single base substitution C T intron_variant PBCA-DE 15 101187602 101187602 single base substitution C T intron_variant PBCA-DE 15 101189294 101189294 insertion of <=200bp - T 3_prime_UTR_variant PBCA-DE 15 101195227 101195227 single base substitution T C downstream_gene_variant PRAD-CA 15 101176197 101176197 single base substitution T G intron_variant PRAD-CA 15 101182376 101182376 single base substitution G A intron_variant PRAD-CA 15 101196334 101196334 single base substitution G T downstream_gene_variant PRAD-UK 15 101156057 101156057 single base substitution G C downstream_gene_variant PRAD-UK 15 101156057 101156057 single base substitution G C intron_variant PRAD-UK 15 101157608 101157608 single base substitution T G downstream_gene_variant PRAD-UK 15 101157608 101157608 single base substitution T G intron_variant PRAD-UK 15 101186357 101186357 single base substitution C G intron_variant PRAD-UK 15 101188855 101188855 single base substitution A T 3_prime_UTR_variant PRAD-UK 15 101190995 101190995 single base substitution A C 3_prime_UTR_variant PRAD-UK 15 101190995 101190995 single base substitution A C downstream_gene_variant PRAD-US 15 101169708 101169708 single base substitution G A intron_variant PRAD-US 15 101169708 101169708 single base substitution G A missense_variant R93Q 278G>A RECA-EU 15 101138099 101138099 single base substitution A G upstream_gene_variant RECA-EU 15 101141414 101141414 single base substitution G A upstream_gene_variant RECA-EU 15 101145588 101145588 single base substitution A T intron_variant RECA-EU 15 101145588 101145588 single base substitution A T upstream_gene_variant RECA-EU 15 101150041 101150041 single base substitution G A intron_variant RECA-EU 15 101150041 101150041 single base substitution G A splice_region_variant RECA-EU 15 101155297 101155297 single base substitution C T downstream_gene_variant RECA-EU 15 101155297 101155297 single base substitution C T intron_variant RECA-EU 15 101170552 101170552 single base substitution A G downstream_gene_variant RECA-EU 15 101170552 101170552 single base substitution A G intron_variant RECA-EU 15 101173067 101173067 single base substitution A C downstream_gene_variant RECA-EU 15 101173067 101173067 single base substitution A C intron_variant RECA-EU 15 101173467 101173467 single base substitution G T downstream_gene_variant RECA-EU 15 101173467 101173467 single base substitution G T intron_variant RECA-EU 15 101182701 101182701 single base substitution T C intron_variant RECA-EU 15 101183685 101183685 single base substitution T C intron_variant RECA-EU 15 101187477 101187477 single base substitution C T intron_variant RECA-EU 15 101188220 101188220 single base substitution A G intron_variant SKCA-BR 15 101142637 101142637 single base substitution T G upstream_gene_variant SKCA-BR 15 101143622 101143622 insertion of <=200bp - AC intron_variant SKCA-BR 15 101145245 101145245 single base substitution G A intron_variant SKCA-BR 15 101145245 101145245 single base substitution G A upstream_gene_variant SKCA-BR 15 101148600 101148600 single base substitution C T intron_variant SKCA-BR 15 101148600 101148600 single base substitution C T upstream_gene_variant SKCA-BR 15 101149882 101149882 single base substitution C T exon_variant SKCA-BR 15 101149882 101149882 single base substitution C T intron_variant SKCA-BR 15 101150890 101150890 single base substitution C T intron_variant SKCA-BR 15 101151021 101151021 single base substitution T A intron_variant SKCA-BR 15 101152128 101152128 single base substitution C T intron_variant SKCA-BR 15 101153957 101153957 single base substitution C T downstream_gene_variant SKCA-BR 15 101153957 101153957 single base substitution C T intron_variant SKCA-BR 15 101154802 101154802 single base substitution T G downstream_gene_variant SKCA-BR 15 101154802 101154802 single base substitution T G intron_variant SKCA-BR 15 101156338 101156338 single base substitution G T downstream_gene_variant SKCA-BR 15 101156338 101156338 single base substitution G T intron_variant SKCA-BR 15 101156363 101156363 single base substitution A C downstream_gene_variant SKCA-BR 15 101156363 101156363 single base substitution A C intron_variant SKCA-BR 15 101162193 101162193 single base substitution G A intron_variant SKCA-BR 15 101162405 101162405 insertion of <=200bp - CAAAAAGA intron_variant SKCA-BR 15 101169080 101169080 single base substitution T G intron_variant SKCA-BR 15 101169197 101169197 single base substitution T A intron_variant SKCA-BR 15 101169198 101169198 single base substitution C T intron_variant SKCA-BR 15 101173431 101173431 single base substitution G A downstream_gene_variant SKCA-BR 15 101173431 101173431 single base substitution G A intron_variant SKCA-BR 15 101178632 101178632 single base substitution C T intron_variant SKCA-BR 15 101179193 101179193 single base substitution G A intron_variant SKCA-BR 15 101180811 101180811 single base substitution A G intron_variant SKCA-BR 15 101182809 101182810 deletion of <=200bp AG - intron_variant SKCA-BR 15 101183557 101183557 single base substitution C T intron_variant SKCA-BR 15 101186237 101186237 single base substitution C T intron_variant SKCA-BR 15 101195536 101195536 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 15 101196459 101196459 single base substitution A G downstream_gene_variant SKCA-BR 15 101196732 101196732 single base substitution G A downstream_gene_variant SKCM-US 15 101169997 101169997 single base substitution C T intron_variant SKCM-US 15 101169997 101169997 single base substitution C T synonymous_variant I189I 567C>T SKCM-US 15 101188569 101188569 single base substitution C T stop_gained R287* 859C>T SKCM-US 15 101188569 101188569 single base substitution C T stop_gained R85* 253C>T STAD-US 15 101152540 101152540 single base substitution C T exon_variant STAD-US 15 101152540 101152540 single base substitution C T missense_variant P40L 119C>T STAD-US 15 101152629 101152629 single base substitution G A exon_variant STAD-US 15 101152629 101152629 single base substitution G A missense_variant G70R 208G>A STAD-US 15 101169958 101169958 single base substitution C T intron_variant STAD-US 15 101169958 101169958 single base substitution C T synonymous_variant I176I 528C>T STAD-US 15 101169989 101169989 single base substitution G A intron_variant STAD-US 15 101169989 101169989 single base substitution G A missense_variant A187T 559G>A STAD-US 15 101170038 101170038 single base substitution G T intron_variant STAD-US 15 101170038 101170038 single base substitution G T missense_variant G203V 608G>T STAD-US 15 101170069 101170069 single base substitution C T intron_variant STAD-US 15 101170069 101170069 single base substitution C T synonymous_variant D213D 639C>T STAD-US 15 101170100 101170100 single base substitution A G intron_variant STAD-US 15 101170100 101170100 single base substitution A G missense_variant R224G 670A>G STAD-US 15 101170193 101170193 single base substitution A G intron_variant STAD-US 15 101170193 101170193 single base substitution A G missense_variant I255V 763A>G STAD-US 15 101188577 101188577 single base substitution T C synonymous_variant C289C 867T>C STAD-US 15 101188577 101188577 single base substitution T C synonymous_variant C87C 261T>C THCA-SA 15 101190032 101190032 single base substitution G A 3_prime_UTR_variant THCA-SA 15 101190032 101190032 single base substitution G A downstream_gene_variant UCEC-US 15 101152580 101152580 single base substitution C A exon_variant UCEC-US 15 101152580 101152580 single base substitution C A missense_variant F53L 159C>A UCEC-US 15 101152611 101152611 single base substitution C T exon_variant UCEC-US 15 101152611 101152611 single base substitution C T missense_variant R64W 190C>T UCEC-US 15 101152628 101152628 single base substitution C T exon_variant UCEC-US 15 101152628 101152628 single base substitution C T synonymous_variant H69H 207C>T UCEC-US 15 101169707 101169707 single base substitution C T intron_variant UCEC-US 15 101169707 101169707 single base substitution C T missense_variant R93W 277C>T UCEC-US 15 101188569 101188569 single base substitution C T stop_gained R287* 859C>T UCEC-US 15 101188569 101188569 single base substitution C T stop_gained R85* 253C>T UCEC-US 15 101188602 101188602 single base substitution C T missense_variant L298F 892C>T UCEC-US 15 101188602 101188602 single base substitution C T missense_variant L96F 286C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BS-A0TJ-01 COSM959578 c.277C>T p.R93W Substitution - Missense 15:100629502-100629502 + TCGA-IN-7808-01 COSM4053442 c.559G>A p.A187T Substitution - Missense 15:100629784-100629784 + TCGA-BR-4368-01 COSM4053440 c.208G>A p.G70R Substitution - Missense 15:100612424-100612424 + LUAD-S00484 COSM392348 c.908delT p.I303fs*5 Deletion - Frameshift 15:100648413-100648413 + PT36 COSM5916412 c.154C>T p.H52Y Substitution - Missense 15:100612370-100612370 + HCC2998 COSM2200346 c.632T>C p.L211S Substitution - Missense 15:100629857-100629857 + KYSE-450 COSM2200350 c.827G>A p.R276K Substitution - Missense 15:100648332-100648332 + TCGA-HT-8104-01 COSM3968998 c.784C>T p.R262* Substitution - Nonsense 15:100630009-100630009 + TCGA-D1-A16X-01 COSM959579 c.859C>T p.R287* Substitution - Nonsense 15:100648364-100648364 + TCGA-G4-6320-01 COSM3690321 c.292C>T p.R98C Substitution - Missense 15:100629517-100629517 + ccRCC-53 COSM1660640 c.56A>T p.Q19L Substitution - Missense 15:100612272-100612272 + TCGA-BS-A0UL-01 COSM959577 c.207C>T p.H69H Substitution - coding silent 15:100612423-100612423 + PD11346a COSM5793958 c.144G>A p.W48* Substitution - Nonsense 15:100612360-100612360 + TCGA-34-5232-01 COSM699642 c.553C>T p.R185* Substitution - Nonsense 15:100629778-100629778 + TCGA-DM-A0XD-01 COSM1375676 c.785G>A p.R262Q Substitution - Missense 15:100630010-100630010 + HT115 COSM959579 c.859C>T p.R287* Substitution - Nonsense 15:100648364-100648364 + CSCC-49-T COSM4553920 c.605G>A p.R202K Substitution - Missense 15:100629830-100629830 + ZZUFHECRKL-G019T COSM554361 c.628C>T p.R210C Substitution - Missense 15:100629853-100629853 + TCGA-FP-A4BE-01 COSM4053443 c.608G>T p.G203V Substitution - Missense 15:100629833-100629833 + SNU-C4 COSM1375675 c.459G>A p.P153P Substitution - coding silent 15:100629684-100629684 + TCGA-GF-A6C9-06 COSM959579 c.859C>T p.R287* Substitution - Nonsense 15:100648364-100648364 + TCGA-B7-5818-01 COSM4053444 c.639C>T p.D213D Substitution - coding silent 15:100629864-100629864 + TCGA-B5-A11Y-01 COSM959576 c.190C>T p.R64W Substitution - Missense 15:100612406-100612406 + TCGA-AP-A0LM-01 COSM959579 c.859C>T p.R287* Substitution - Nonsense 15:100648364-100648364 + TCGA-BF-A1PX-01 COSM4905103 c.567C>T p.I189I Substitution - coding silent 15:100629792-100629792 + TCGA-HC-7232-01 COSM4393621 c.278G>A p.R93Q Substitution - Missense 15:100629503-100629503 + WA20 COSM238855 c.199C>G p.L67V Substitution - Missense 15:100612415-100612415 + ESCC-004T COSM2200335 c.91C>T p.R31* Substitution - Nonsense 15:100612307-100612307 + pfg050T COSM554361 c.628C>T p.R210C Substitution - Missense 15:100629853-100629853 + 587222 COSM256353 c.944T>G p.F315C Substitution - Missense 15:100648449-100648449 + TCGA-AG-3892-01 COSM256353 c.944T>G p.F315C Substitution - Missense 15:100648449-100648449 + 587376 COSM1183746 c.910G>T p.A304S Substitution - Missense 15:100648415-100648415 + TCGA-A7-A0DA-01 COSM433590 c.211+1_211+4delGTGA p.? Unknown AOCS-079-1-1 COSM3943949 c.442G>A p.D148N Substitution - Missense 15:100629667-100629667 + NOKSI COSM4595370 c.230A>T p.D77V Substitution - Missense 15:100629455-100629455 + U2940 COSM2200350 c.827G>A p.R276K Substitution - Missense 15:100648332-100648332 + TCGA-CG-4441-01 COSM4053441 c.528C>T p.I176I Substitution - coding silent 15:100629753-100629753 + TCGA-AD-6890-01 COSM1375675 c.459G>A p.P153P Substitution - coding silent 15:100629684-100629684 + TCGA-HE-A5NI-01 COSM4414184 c.67G>A p.A23T Substitution - Missense 15:100612283-100612283 + TCGA-85-6560-01 COSM699643 c.458C>T p.P153L Substitution - Missense 15:100629683-100629683 + TCGA-D5-6928-01 COSM1375674 c.116delC p.P40fs*28 Deletion - Frameshift 15:100612332-100612332 + C086 COSM5527007 c.59C>T p.A20V Substitution - Missense 15:100612275-100612275 + TCGA-CD-8525-01 COSM4053446 c.763A>G p.I255V Substitution - Missense 15:100629988-100629988 + TCGA-BR-4256-01 COSM4053447 c.867T>C p.C289C Substitution - coding silent 15:100648372-100648372 + TCGA-D1-A103-01 COSM959580 c.892C>T p.L298F Substitution - Missense 15:100648397-100648397 + BRC4 COSM4053439 c.119C>T p.P40L Substitution - Missense 15:100612335-100612335 + LS174T COSM4645890 c.371C>T p.A124V Substitution - Missense 15:100629596-100629596 + TCGA-AN-A0AL-01 COSM433591 c.344A>G p.N115S Substitution - Missense 15:100629569-100629569 + Pat_63_A COSM5848856 c.562G>A p.V188M Substitution - Missense 15:100629787-100629787 + TCGA-AP-A056-01 COSM959575 c.159C>A p.F53L Substitution - Missense 15:100612375-100612375 + TCGA-B8-4151-01 COSM470416 c.408C>T p.L136L Substitution - coding silent 15:100629633-100629633 + DN12035 COSM5793958 c.144G>A p.W48* Substitution - Nonsense 15:100612360-100612360 + CSCC-32-T COSM4532795 c.191G>A p.R64Q Substitution - Missense 15:100612407-100612407 + TCGA-BR-8591-01 COSM4053439 c.119C>T p.P40L Substitution - Missense 15:100612335-100612335 + PD4100a COSM159215 c.426G>A p.E142E Substitution - coding silent 15:100629651-100629651 + TCGA-BR-4201-01 COSM4053445 c.670A>G p.R224G Substitution - Missense 15:100629895-100629895 + 24T COSM108520 c.194T>G p.V65G Substitution - Missense 15:100612410-100612410 + TCGA-AN-A046-01 COSM3815659 c.848G>A p.R283Q Substitution - Missense 15:100648353-100648353 + ccRCC-53 COSM1660641 c.57G>T p.Q19H Substitution - Missense 15:100612273-100612273 + ME009T COSM223820 c.320G>A p.S107N Substitution - Missense 15:100629545-100629545 + TCGA-66-2781-01 COSM699641 c.904C>G p.P302A Substitution - Missense 15:100648409-100648409 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.31841;Hs.31845

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.M100V c.298A>G 15 101169728 COREAD A G Missense p.N115S c.344A>G 15 101169774 BRCA A G Missense p.R224G c.670A>G 15 101170100 STAD A T IntronicSNV . c.817+8325A>T 15 101178572 HC A T Missense p.T206S c.616A>T 15 101170046 LUAD C G Missense p.P302A c.904C>G 15 101188614 LUSC C T 5-UTRSNV . c.1-43C>T 15 101152379 CM C T Missense p.P153L c.458C>T 15 101169888 LUSC C T Missense p.P40L c.119C>T 15 101152540 BRCA C T Missense p.R210C c.628C>T 15 101170058 LUAD C T Missense p.R64W c.190C>T 15 101152611 UCEC C T Missense p.R93W c.277C>T 15 101169707 UCEC C T Nonsense p.R185* c.553C>T 15 101169983 LUSC C T Synonymous p.D213D c.639C>T 15 101170069 STAD C T Synonymous p.H69H c.207C>T 15 101152628 UCEC C T Synonymous p.I176I c.528C>T 15 101169958 STAD C T Synonymous p.I189I c.567C>T 15 101169997 CM C T Synonymous p.Y236Y c.708C>T 15 101170138 LUAD G A IntronicSNV . c.818-1808G>A 15 101186720 CM G A Missense p.A112T c.334G>A 15 101169764 HNSC G A Missense p.G70R c.208G>A 15 101152629 STAD G A Missense p.R93Q c.278G>A 15 101169708 PRAD G A Missense p.S107N c.320G>A 15 101169750 CM G A Synonymous p.E142E c.426G>A 15 101169856 BRCA GTGA - SpliceDonorDeletion . c.211+3_211+6delGAGT 15 101152633 BRCA T C IntronicSNV . c.817+60T>C 15 101170307 CM T C Synonymous p.C289C c.867T>C 15 101188577 STAD