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 17 26666706 26666706 + Silent SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr17:26666706C>T c.159C>T c.(157-159)ctC>ctT p.L53L BLCA 17 26667448 26667448 + Missense_Mutation SNP G G A TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr17:26667448G>A c.319G>A c.(319-321)Gaa>Aaa p.E107K BLCA 17 26669328 26669328 + Missense_Mutation SNP C C T TCGA-GC-A3OO-01A-11D-A22Z-08 TCGA-GC-A3OO-10C-01D-A22Z-08 g.chr17:26669328C>T c.574C>T c.(574-576)Cgc>Tgc p.R192C BLCA 17 26669438 26669438 + Silent SNP C C T TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr17:26669438C>T c.684C>T c.(682-684)atC>atT p.I228I BRCA 17 26671409 26671409 + Missense_Mutation SNP G G A TCGA-AC-A2FM-01A-11D-A19Y-09 TCGA-AC-A2FM-11B-32D-A19Y-09 g.chr17:26671409G>A c.734G>A c.(733-735)cGa>cAa p.R245Q COAD 17 26668321 26668321 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr17:26668321A>G c.434A>G c.(433-435)gAg>gGg p.E145G COAD 17 26668433 26668433 + Missense_Mutation SNP G G A TCGA-AD-6888-01A-11D-1924-10 TCGA-AD-6888-10A-01D-1924-10 g.chr17:26668433G>A c.469G>A c.(469-471)Gtg>Atg p.V157M COAD 17 26669304 26669304 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:26669304G>A c.550G>A c.(550-552)Gag>Aag p.E184K COAD 17 26669341 26669341 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:26669341G>A c.587G>A c.(586-588)cGc>cAc p.R196H COADREAD 17 26668321 26668321 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr17:26668321A>G c.434A>G c.(433-435)gAg>gGg p.E145G COADREAD 17 26668433 26668433 + Missense_Mutation SNP G G A TCGA-AD-6888-01A-11D-1924-10 TCGA-AD-6888-10A-01D-1924-10 g.chr17:26668433G>A c.469G>A c.(469-471)Gtg>Atg p.V157M COADREAD 17 26669303 26669303 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:26669303C>T c.549C>T c.(547-549)atC>atT p.I183I COADREAD 17 26669304 26669304 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:26669304G>A c.550G>A c.(550-552)Gag>Aag p.E184K COADREAD 17 26669341 26669341 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:26669341G>A c.587G>A c.(586-588)cGc>cAc p.R196H ESCA 17 26667392 26667392 + Missense_Mutation SNP G G C TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr17:26667392G>C c.263G>C c.(262-264)cGa>cCa p.R88P GBM 17 26666722 26666722 + Missense_Mutation SNP G G A TCGA-19-5959-01A-11D-1696-08 TCGA-19-5959-11A-01D-1696-08 g.chr17:26666722G>A c.175G>A c.(175-177)Ggg>Agg p.G59R GBMLGG 17 26666704 26666704 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:26666704C>T c.157C>T c.(157-159)Ctc>Ttc p.L53F GBMLGG 17 26666722 26666722 + Missense_Mutation SNP G G A TCGA-19-5959-01A-11D-1696-08 TCGA-19-5959-11A-01D-1696-08 g.chr17:26666722G>A c.175G>A c.(175-177)Ggg>Agg p.G59R GBMLGG 17 26668285 26668285 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:26668285C>A c.398C>A c.(397-399)cCt>cAt p.P133H HNSC 17 26666552 26666552 + Missense_Mutation SNP C C T TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr17:26666552C>T c.5C>T c.(4-6)tCg>tTg p.S2L HNSC 17 26669278 26669278 + Missense_Mutation SNP C C G TCGA-CX-7085-01A-21D-2012-08 TCGA-CX-7085-10A-01D-2013-08 g.chr17:26669278C>G c.524C>G c.(523-525)tCt>tGt p.S175C HNSC 17 26671444 26671444 + Missense_Mutation SNP G G A TCGA-D6-A6EQ-01A-11D-A31L-08 TCGA-D6-A6EQ-10A-01D-A31J-08 g.chr17:26671444G>A c.769G>A c.(769-771)Gag>Aag p.E257K HNSC 17 26671454 26671454 + Missense_Mutation SNP G G A TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr17:26671454G>A c.779G>A c.(778-780)cGc>cAc p.R260H KIPAN 17 26667402 26667402 + Silent SNP C C T TCGA-B8-4620-01A-02D-1386-10 TCGA-B8-4620-10A-01D-1251-10 g.chr17:26667402C>T c.273C>T c.(271-273)acC>acT p.T91T KIPAN 17 26669383 26669383 + Missense_Mutation SNP G G A TCGA-CZ-4854-01A-01D-1373-10 TCGA-CZ-4854-11A-01D-1373-10 g.chr17:26669383G>A c.629G>A c.(628-630)tGc>tAc p.C210Y KIRC 17 26667402 26667402 + Silent SNP C C T TCGA-B8-4620-01A-02D-1386-10 TCGA-B8-4620-10A-01D-1251-10 g.chr17:26667402C>T c.273C>T c.(271-273)acC>acT p.T91T KIRC 17 26669383 26669383 + Missense_Mutation SNP G G A TCGA-CZ-4854-01A-01D-1373-10 TCGA-CZ-4854-11A-01D-1373-10 g.chr17:26669383G>A c.629G>A c.(628-630)tGc>tAc p.C210Y LGG 17 26666704 26666704 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:26666704C>T c.157C>T c.(157-159)Ctc>Ttc p.L53F LGG 17 26668285 26668285 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:26668285C>A c.398C>A c.(397-399)cCt>cAt p.P133H LUAD 17 26666553 26666553 + Silent SNP G G A TCGA-86-8668-01A-11D-2393-08 TCGA-86-8668-10A-01D-2393-08 g.chr17:26666553G>A c.6G>A c.(4-6)tcG>tcA p.S2S LUAD 17 26667374 26667374 + Missense_Mutation SNP C C A TCGA-55-7576-01A-11D-2063-08 TCGA-55-7576-10A-01D-2063-08 g.chr17:26667374C>A c.245C>A c.(244-246)aCc>aAc p.T82N PCPG 17 26671480 26671492 + Frame_Shift_Del DEL GCCACAAGCCGTA GCCACAAGCCGTA - TCGA-S7-A7X2-01A-12D-A35I-08 TCGA-S7-A7X2-10A-01D-A35G-08 g.chr17:26671480_26671492delGCCACAAGCCGTA c.805_817delGCCACAAGCCGTA c.(805-819)gccacaagccgtagcfs p.ATSRS269fs PRAD 17 26666643 26666643 + Silent SNP C C A TCGA-KK-A6E7-01A-11D-A31L-08 TCGA-KK-A6E7-11A-11D-A31J-08 g.chr17:26666643C>A c.96C>A c.(94-96)ctC>ctA p.L32L READ 17 26669303 26669303 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:26669303C>T c.549C>T c.(547-549)atC>atT p.I183I SARC 17 26671442 26671442 + Missense_Mutation SNP A A G TCGA-DX-A6YX-01A-11D-A417-09 TCGA-DX-A6YX-10B-01D-A41A-09 g.chr17:26671442A>G c.767A>G c.(766-768)tAt>tGt p.Y256C SKCM 17 26669304 26669304 + Missense_Mutation SNP G G A TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr17:26669304G>A c.550G>A c.(550-552)Gag>Aag p.E184K SKCM 17 26669339 26669339 + Silent SNP C C T TCGA-ER-A19W-06A-41D-A23B-08 TCGA-ER-A19W-10A-01D-A23B-08 g.chr17:26669339C>T c.585C>T c.(583-585)ggC>ggT p.G195G SKCM 17 26671537 26671537 + Silent SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr17:26671537C>T c.862C>T c.(862-864)Ctg>Ttg p.L288L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 17 26669328 26669328 single base substitution C T downstream_gene_variant BLCA-US 17 26669328 26669328 single base substitution C T exon_variant BLCA-US 17 26669328 26669328 single base substitution C T missense_variant R192C 574C>T BLCA-US 17 26669328 26669328 single base substitution C T missense_variant R88C 262C>T BRCA-EU 17 26658428 26658428 single base substitution C T upstream_gene_variant BRCA-EU 17 26660966 26660966 single base substitution A C upstream_gene_variant BRCA-EU 17 26660968 26660968 single base substitution C A upstream_gene_variant BRCA-EU 17 26660969 26660969 insertion of <=200bp - A upstream_gene_variant BRCA-EU 17 26661758 26661758 single base substitution T C upstream_gene_variant BRCA-EU 17 26662835 26662835 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 17 26662835 26662835 single base substitution C T exon_variant BRCA-EU 17 26662835 26662835 single base substitution C T intron_variant BRCA-EU 17 26662835 26662835 single base substitution C T upstream_gene_variant BRCA-EU 17 26664421 26664421 single base substitution T G intron_variant BRCA-EU 17 26664421 26664421 single base substitution T G upstream_gene_variant BRCA-EU 17 26665248 26665248 single base substitution C T intron_variant BRCA-EU 17 26665248 26665248 single base substitution C T upstream_gene_variant BRCA-EU 17 26665510 26665510 single base substitution C A intron_variant BRCA-EU 17 26665510 26665510 single base substitution C A upstream_gene_variant BRCA-EU 17 26669007 26669007 single base substitution C G downstream_gene_variant BRCA-EU 17 26669007 26669007 single base substitution C G intron_variant BRCA-EU 17 26669158 26669159 deletion of <=200bp TC - downstream_gene_variant BRCA-EU 17 26669158 26669159 deletion of <=200bp TC - intron_variant BRCA-EU 17 26670583 26670583 single base substitution C A downstream_gene_variant BRCA-EU 17 26670583 26670583 single base substitution C A intron_variant BRCA-EU 17 26671534 26671534 single base substitution G C downstream_gene_variant BRCA-EU 17 26671534 26671534 single base substitution G C exon_variant BRCA-EU 17 26671534 26671534 single base substitution G C missense_variant E183Q 547G>C BRCA-EU 17 26671534 26671534 single base substitution G C missense_variant E287Q 859G>C BRCA-EU 17 26671884 26671884 single base substitution C G 3_prime_UTR_variant BRCA-EU 17 26671884 26671884 single base substitution C G downstream_gene_variant BRCA-EU 17 26672301 26672301 single base substitution G C 3_prime_UTR_variant BRCA-EU 17 26672301 26672301 single base substitution G C downstream_gene_variant BRCA-EU 17 26673133 26673133 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 26673133 26673133 single base substitution C T downstream_gene_variant BRCA-EU 17 26673275 26673275 single base substitution G A 3_prime_UTR_variant BRCA-EU 17 26673275 26673275 single base substitution G A downstream_gene_variant BRCA-EU 17 26673315 26673315 single base substitution G C 3_prime_UTR_variant BRCA-EU 17 26673315 26673315 single base substitution G C downstream_gene_variant BRCA-EU 17 26673480 26673480 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 26673480 26673480 single base substitution C T downstream_gene_variant BRCA-EU 17 26674143 26674143 single base substitution A T downstream_gene_variant BRCA-EU 17 26677181 26677181 single base substitution C T downstream_gene_variant BRCA-FR 17 26662894 26662894 single base substitution G A intron_variant BRCA-FR 17 26662894 26662894 single base substitution G A upstream_gene_variant BRCA-FR 17 26673016 26673016 single base substitution G A 3_prime_UTR_variant BRCA-FR 17 26673016 26673016 single base substitution G A downstream_gene_variant BRCA-UK 17 26657862 26657862 single base substitution C T upstream_gene_variant BRCA-UK 17 26669875 26669875 single base substitution G A downstream_gene_variant BRCA-UK 17 26669875 26669875 single base substitution G A intron_variant BRCA-UK 17 26678520 26678520 single base substitution C T downstream_gene_variant BRCA-US 17 26658938 26658938 single base substitution T A upstream_gene_variant BRCA-US 17 26671409 26671409 single base substitution G A downstream_gene_variant BRCA-US 17 26671409 26671409 single base substitution G A exon_variant BRCA-US 17 26671409 26671409 single base substitution G A missense_variant R141Q 422G>A BRCA-US 17 26671409 26671409 single base substitution G A missense_variant R245Q 734G>A BRCA-US 17 26677509 26677509 single base substitution G A downstream_gene_variant BTCA-JP 17 26671553 26671553 single base substitution G A downstream_gene_variant BTCA-JP 17 26671553 26671553 single base substitution G A missense_variant R189H 566G>A BTCA-JP 17 26671553 26671553 single base substitution G A missense_variant R293H 878G>A BTCA-JP 17 26676044 26676044 single base substitution T G downstream_gene_variant COAD-US 17 26668433 26668433 single base substitution G A downstream_gene_variant COAD-US 17 26668433 26668433 single base substitution G A exon_variant COAD-US 17 26668433 26668433 single base substitution G A missense_variant V157M 469G>A COAD-US 17 26668433 26668433 single base substitution G A missense_variant V53M 157G>A COCA-CN 17 26669381 26669381 single base substitution C T downstream_gene_variant COCA-CN 17 26669381 26669381 single base substitution C T exon_variant COCA-CN 17 26669381 26669381 single base substitution C T synonymous_variant C105C 315C>T COCA-CN 17 26669381 26669381 single base substitution C T synonymous_variant C209C 627C>T ESAD-UK 17 26658114 26658114 single base substitution C T upstream_gene_variant ESAD-UK 17 26660816 26660816 single base substitution A G upstream_gene_variant ESAD-UK 17 26663463 26663463 single base substitution G T intron_variant ESAD-UK 17 26663463 26663463 single base substitution G T upstream_gene_variant ESAD-UK 17 26663467 26663467 single base substitution G T intron_variant ESAD-UK 17 26663467 26663467 single base substitution G T upstream_gene_variant ESAD-UK 17 26663577 26663577 single base substitution G T 5_prime_UTR_variant ESAD-UK 17 26663577 26663577 single base substitution G T intron_variant ESAD-UK 17 26663577 26663577 single base substitution G T upstream_gene_variant ESAD-UK 17 26667678 26667678 single base substitution C T downstream_gene_variant ESAD-UK 17 26667678 26667678 single base substitution C T intron_variant ESAD-UK 17 26670768 26670768 single base substitution A G downstream_gene_variant ESAD-UK 17 26670768 26670768 single base substitution A G intron_variant ESAD-UK 17 26672094 26672094 single base substitution A G 3_prime_UTR_variant ESAD-UK 17 26672094 26672094 single base substitution A G downstream_gene_variant ESAD-UK 17 26673327 26673327 single base substitution T C 3_prime_UTR_variant ESAD-UK 17 26673327 26673327 single base substitution T C downstream_gene_variant ESAD-UK 17 26676081 26676081 single base substitution G C downstream_gene_variant ESAD-UK 17 26676900 26676900 single base substitution T G downstream_gene_variant ESCA-CN 17 26667456 26667456 single base substitution G T downstream_gene_variant ESCA-CN 17 26667456 26667456 single base substitution G T intron_variant ESCA-CN 17 26667456 26667456 single base substitution G T missense_variant K109N 327G>T ESCA-CN 17 26667456 26667456 single base substitution G T missense_variant K5N 15G>T ESCA-CN 17 26668320 26668320 single base substitution G A downstream_gene_variant ESCA-CN 17 26668320 26668320 single base substitution G A exon_variant ESCA-CN 17 26668320 26668320 single base substitution G A missense_variant E145K 433G>A ESCA-CN 17 26668320 26668320 single base substitution G A missense_variant E41K 121G>A ESCA-CN 17 26668338 26668338 single base substitution G A downstream_gene_variant ESCA-CN 17 26668338 26668338 single base substitution G A exon_variant ESCA-CN 17 26668338 26668338 single base substitution G A missense_variant E151K 451G>A ESCA-CN 17 26668338 26668338 single base substitution G A missense_variant E47K 139G>A ESCA-CN 17 26671462 26671462 single base substitution G A downstream_gene_variant ESCA-CN 17 26671462 26671462 single base substitution G A exon_variant ESCA-CN 17 26671462 26671462 single base substitution G A missense_variant D159N 475G>A ESCA-CN 17 26671462 26671462 single base substitution G A missense_variant D263N 787G>A GBM-US 17 26675209 26675209 single base substitution C A downstream_gene_variant KIRC-US 17 26667402 26667402 single base substitution C T 5_prime_UTR_variant KIRC-US 17 26667402 26667402 single base substitution C T intron_variant KIRC-US 17 26667402 26667402 single base substitution C T synonymous_variant T91T 273C>T KIRC-US 17 26667402 26667402 single base substitution C T upstream_gene_variant KIRC-US 17 26669383 26669383 single base substitution G A downstream_gene_variant KIRC-US 17 26669383 26669383 single base substitution G A exon_variant KIRC-US 17 26669383 26669383 single base substitution G A missense_variant C106Y 317G>A KIRC-US 17 26669383 26669383 single base substitution G A missense_variant C210Y 629G>A KIRP-US 17 26675218 26675218 deletion of <=200bp A - downstream_gene_variant LAML-KR 17 26678960 26678960 single base substitution G C downstream_gene_variant LICA-FR 17 26660099 26660099 insertion of <=200bp - ACACAC upstream_gene_variant LICA-FR 17 26666267 26666267 single base substitution G A intron_variant LICA-FR 17 26666267 26666267 single base substitution G A upstream_gene_variant LICA-FR 17 26666268 26666268 deletion of <=200bp A - intron_variant LICA-FR 17 26666268 26666268 deletion of <=200bp A - upstream_gene_variant LICA-FR 17 26673325 26673325 single base substitution A C 3_prime_UTR_variant LICA-FR 17 26673325 26673325 single base substitution A C downstream_gene_variant LINC-JP 17 26659065 26659065 single base substitution T C upstream_gene_variant LINC-JP 17 26660098 26660098 single base substitution A C upstream_gene_variant LINC-JP 17 26660134 26660134 single base substitution A C upstream_gene_variant LINC-JP 17 26661611 26661611 single base substitution C T upstream_gene_variant LINC-JP 17 26668194 26668194 single base substitution A C downstream_gene_variant LINC-JP 17 26668194 26668194 single base substitution A C intron_variant LINC-JP 17 26668234 26668234 single base substitution A C downstream_gene_variant LINC-JP 17 26668234 26668234 single base substitution A C intron_variant LINC-JP 17 26671714 26671714 single base substitution T G 3_prime_UTR_variant LINC-JP 17 26671714 26671714 single base substitution T G downstream_gene_variant LINC-JP 17 26674132 26674143 deletion of <=200bp AGCCAGGTCGTA - downstream_gene_variant LINC-JP 17 26675120 26675120 insertion of <=200bp - GG downstream_gene_variant LINC-JP 17 26677532 26677532 single base substitution G A downstream_gene_variant LIRI-JP 17 26658389 26658389 single base substitution C T upstream_gene_variant LIRI-JP 17 26659119 26659165 deletion of <=200bp CAGGTGTTCCAAAGGATCCCCGTTCCCTCTGCCACCACCTCTCTGAG - upstream_gene_variant LIRI-JP 17 26659361 26659361 single base substitution C A upstream_gene_variant LIRI-JP 17 26659837 26659837 single base substitution A T upstream_gene_variant LIRI-JP 17 26660782 26660782 single base substitution T C upstream_gene_variant LIRI-JP 17 26665006 26665006 single base substitution G A intron_variant LIRI-JP 17 26665006 26665006 single base substitution G A upstream_gene_variant LIRI-JP 17 26665785 26665785 single base substitution T A intron_variant LIRI-JP 17 26665785 26665785 single base substitution T A upstream_gene_variant LIRI-JP 17 26665854 26665854 deletion of <=200bp G - intron_variant LIRI-JP 17 26665854 26665854 deletion of <=200bp G - upstream_gene_variant LIRI-JP 17 26666791 26666791 single base substitution G T intron_variant LIRI-JP 17 26666791 26666791 single base substitution G T upstream_gene_variant LIRI-JP 17 26668747 26668747 single base substitution T A downstream_gene_variant LIRI-JP 17 26668747 26668747 single base substitution T A intron_variant LIRI-JP 17 26670793 26670793 single base substitution C A downstream_gene_variant LIRI-JP 17 26670793 26670793 single base substitution C A intron_variant LIRI-JP 17 26670888 26670888 single base substitution A G downstream_gene_variant LIRI-JP 17 26670888 26670888 single base substitution A G intron_variant LIRI-JP 17 26671382 26671382 single base substitution A G downstream_gene_variant LIRI-JP 17 26671382 26671382 single base substitution A G intron_variant LIRI-JP 17 26671388 26671388 single base substitution A G downstream_gene_variant LIRI-JP 17 26671388 26671388 single base substitution A G splice_acceptor_variant LIRI-JP 17 26671395 26671395 single base substitution A C downstream_gene_variant LIRI-JP 17 26671395 26671395 single base substitution A C exon_variant LIRI-JP 17 26671395 26671395 single base substitution A C missense_variant E136D 408A>C LIRI-JP 17 26671395 26671395 single base substitution A C missense_variant E240D 720A>C LIRI-JP 17 26671986 26671986 single base substitution C A 3_prime_UTR_variant LIRI-JP 17 26671986 26671986 single base substitution C A downstream_gene_variant LIRI-JP 17 26672379 26672380 deletion of <=200bp AG - 3_prime_UTR_variant LIRI-JP 17 26672379 26672380 deletion of <=200bp AG - downstream_gene_variant LIRI-JP 17 26672433 26672433 single base substitution G A 3_prime_UTR_variant LIRI-JP 17 26672433 26672433 single base substitution G A downstream_gene_variant LIRI-JP 17 26672489 26672489 single base substitution G T 3_prime_UTR_variant LIRI-JP 17 26672489 26672489 single base substitution G T downstream_gene_variant LIRI-JP 17 26673478 26673478 single base substitution T G 3_prime_UTR_variant LIRI-JP 17 26673478 26673478 single base substitution T G downstream_gene_variant LIRI-JP 17 26674000 26674001 deletion of <=200bp AA - 3_prime_UTR_variant LIRI-JP 17 26674000 26674001 deletion of <=200bp AA - downstream_gene_variant LIRI-JP 17 26674107 26674107 single base substitution T C downstream_gene_variant LIRI-JP 17 26674405 26674405 single base substitution T C downstream_gene_variant LIRI-JP 17 26676179 26676179 single base substitution A C downstream_gene_variant LIRI-JP 17 26676278 26676278 single base substitution A C downstream_gene_variant LIRI-JP 17 26677950 26677950 single base substitution A G downstream_gene_variant LIRI-JP 17 26678506 26678506 single base substitution C G downstream_gene_variant LUSC-KR 17 26669890 26669890 single base substitution A G downstream_gene_variant LUSC-KR 17 26669890 26669890 single base substitution A G intron_variant LUSC-KR 17 26673316 26673316 single base substitution A T 3_prime_UTR_variant LUSC-KR 17 26673316 26673316 single base substitution A T downstream_gene_variant LUSC-KR 17 26674713 26674713 single base substitution C T downstream_gene_variant LUSC-KR 17 26677544 26677544 single base substitution G A downstream_gene_variant MALY-DE 17 26675956 26675956 single base substitution G T downstream_gene_variant MALY-DE 17 26675957 26675957 single base substitution A T downstream_gene_variant MELA-AU 17 26658088 26658088 single base substitution C T upstream_gene_variant MELA-AU 17 26658421 26658421 single base substitution G A upstream_gene_variant MELA-AU 17 26658681 26658681 single base substitution G A upstream_gene_variant MELA-AU 17 26659789 26659789 single base substitution A G upstream_gene_variant MELA-AU 17 26659834 26659834 single base substitution A T upstream_gene_variant MELA-AU 17 26660251 26660251 single base substitution G A upstream_gene_variant MELA-AU 17 26661720 26661720 single base substitution G A upstream_gene_variant MELA-AU 17 26662101 26662101 single base substitution C T upstream_gene_variant MELA-AU 17 26662523 26662523 single base substitution G A upstream_gene_variant MELA-AU 17 26662581 26662581 single base substitution G A upstream_gene_variant MELA-AU 17 26662584 26662584 single base substitution C T upstream_gene_variant MELA-AU 17 26662678 26662678 single base substitution C T 5_prime_UTR_variant MELA-AU 17 26662678 26662678 single base substitution C T upstream_gene_variant MELA-AU 17 26662726 26662726 single base substitution C T 5_prime_UTR_variant MELA-AU 17 26662726 26662726 single base substitution C T upstream_gene_variant MELA-AU 17 26662811 26662811 single base substitution G A 5_prime_UTR_variant MELA-AU 17 26662811 26662811 single base substitution G A exon_variant MELA-AU 17 26662811 26662811 single base substitution G A intron_variant MELA-AU 17 26662811 26662811 single base substitution G A upstream_gene_variant MELA-AU 17 26662893 26662893 single base substitution G A intron_variant MELA-AU 17 26662893 26662893 single base substitution G A upstream_gene_variant MELA-AU 17 26663698 26663698 single base substitution G T intron_variant MELA-AU 17 26663698 26663698 single base substitution G T upstream_gene_variant MELA-AU 17 26664350 26664350 single base substitution C T intron_variant MELA-AU 17 26664350 26664350 single base substitution C T upstream_gene_variant MELA-AU 17 26664588 26664588 single base substitution C T intron_variant MELA-AU 17 26664588 26664588 single base substitution C T upstream_gene_variant MELA-AU 17 26664645 26664645 single base substitution C T intron_variant MELA-AU 17 26664645 26664645 single base substitution C T upstream_gene_variant MELA-AU 17 26664738 26664738 single base substitution C T intron_variant MELA-AU 17 26664738 26664738 single base substitution C T upstream_gene_variant MELA-AU 17 26664797 26664797 single base substitution C T intron_variant MELA-AU 17 26664797 26664797 single base substitution C T upstream_gene_variant MELA-AU 17 26664920 26664920 single base substitution C T intron_variant MELA-AU 17 26664920 26664920 single base substitution C T upstream_gene_variant MELA-AU 17 26665370 26665370 single base substitution G A intron_variant MELA-AU 17 26665370 26665370 single base substitution G A upstream_gene_variant MELA-AU 17 26665891 26665891 single base substitution C T intron_variant MELA-AU 17 26665891 26665891 single base substitution C T upstream_gene_variant MELA-AU 17 26666577 26666577 single base substitution C T intron_variant MELA-AU 17 26666577 26666577 single base substitution C T synonymous_variant A10A 30C>T MELA-AU 17 26666577 26666577 single base substitution C T upstream_gene_variant MELA-AU 17 26666800 26666800 single base substitution C T intron_variant MELA-AU 17 26666800 26666800 single base substitution C T upstream_gene_variant MELA-AU 17 26667283 26667283 single base substitution C T intron_variant MELA-AU 17 26667283 26667283 single base substitution C T upstream_gene_variant MELA-AU 17 26668301 26668301 single base substitution C T downstream_gene_variant MELA-AU 17 26668301 26668301 single base substitution C T exon_variant MELA-AU 17 26668301 26668301 single base substitution C T synonymous_variant P138P 414C>T MELA-AU 17 26668301 26668301 single base substitution C T synonymous_variant P34P 102C>T MELA-AU 17 26668412 26668412 single base substitution C T downstream_gene_variant MELA-AU 17 26668412 26668412 single base substitution C T intron_variant MELA-AU 17 26668589 26668589 single base substitution G C downstream_gene_variant MELA-AU 17 26668589 26668589 single base substitution G C intron_variant MELA-AU 17 26668835 26668835 single base substitution C T downstream_gene_variant MELA-AU 17 26668835 26668835 single base substitution C T intron_variant MELA-AU 17 26669795 26669795 single base substitution G T downstream_gene_variant MELA-AU 17 26669795 26669795 single base substitution G T intron_variant MELA-AU 17 26670309 26670309 single base substitution C T downstream_gene_variant MELA-AU 17 26670309 26670309 single base substitution C T intron_variant MELA-AU 17 26670793 26670793 single base substitution C T downstream_gene_variant MELA-AU 17 26670793 26670793 single base substitution C T intron_variant MELA-AU 17 26671342 26671342 single base substitution C T downstream_gene_variant MELA-AU 17 26671342 26671342 single base substitution C T intron_variant MELA-AU 17 26671524 26671524 single base substitution G A downstream_gene_variant MELA-AU 17 26671524 26671524 single base substitution G A exon_variant MELA-AU 17 26671524 26671524 single base substitution G A synonymous_variant E179E 537G>A MELA-AU 17 26671524 26671524 single base substitution G A synonymous_variant E283E 849G>A MELA-AU 17 26671585 26671585 single base substitution G A downstream_gene_variant MELA-AU 17 26671585 26671585 single base substitution G A missense_variant D200N 598G>A MELA-AU 17 26671585 26671585 single base substitution G A missense_variant D304N 910G>A MELA-AU 17 26672361 26672361 single base substitution C T 3_prime_UTR_variant MELA-AU 17 26672361 26672361 single base substitution C T downstream_gene_variant MELA-AU 17 26672549 26672549 single base substitution C T 3_prime_UTR_variant MELA-AU 17 26672549 26672549 single base substitution C T downstream_gene_variant MELA-AU 17 26672995 26672995 single base substitution C T 3_prime_UTR_variant MELA-AU 17 26672995 26672995 single base substitution C T downstream_gene_variant MELA-AU 17 26673186 26673186 single base substitution G A 3_prime_UTR_variant MELA-AU 17 26673186 26673186 single base substitution G A downstream_gene_variant MELA-AU 17 26673188 26673188 single base substitution A T 3_prime_UTR_variant MELA-AU 17 26673188 26673188 single base substitution A T downstream_gene_variant MELA-AU 17 26674466 26674466 single base substitution C T downstream_gene_variant MELA-AU 17 26675407 26675407 single base substitution G A downstream_gene_variant MELA-AU 17 26676119 26676119 single base substitution C A downstream_gene_variant MELA-AU 17 26676251 26676251 single base substitution G A downstream_gene_variant MELA-AU 17 26676289 26676289 single base substitution C T downstream_gene_variant MELA-AU 17 26676804 26676804 single base substitution G A downstream_gene_variant MELA-AU 17 26677249 26677249 single base substitution G A downstream_gene_variant MELA-AU 17 26677987 26677987 single base substitution G A downstream_gene_variant MELA-AU 17 26678632 26678633 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant ORCA-IN 17 26673097 26673097 insertion of <=200bp - A 3_prime_UTR_variant ORCA-IN 17 26673097 26673097 insertion of <=200bp - A downstream_gene_variant ORCA-IN 17 26676834 26676834 single base substitution G A downstream_gene_variant ORCA-IN 17 26677524 26677524 single base substitution C A downstream_gene_variant OV-AU 17 26665021 26665021 single base substitution C G intron_variant OV-AU 17 26665021 26665021 single base substitution C G upstream_gene_variant OV-AU 17 26674469 26674469 single base substitution G A downstream_gene_variant OV-AU 17 26676435 26676435 single base substitution G A downstream_gene_variant PACA-AU 17 26659111 26659111 single base substitution C A upstream_gene_variant PACA-AU 17 26665144 26665144 single base substitution T G intron_variant PACA-AU 17 26665144 26665144 single base substitution T G upstream_gene_variant PACA-AU 17 26665283 26665283 single base substitution C G intron_variant PACA-AU 17 26665283 26665283 single base substitution C G upstream_gene_variant PACA-AU 17 26666610 26666610 single base substitution G T intron_variant PACA-AU 17 26666610 26666610 single base substitution G T missense_variant K21N 63G>T PACA-AU 17 26666610 26666610 single base substitution G T upstream_gene_variant PACA-AU 17 26666991 26666991 single base substitution C T intron_variant PACA-AU 17 26666991 26666991 single base substitution C T upstream_gene_variant PACA-AU 17 26671428 26671428 single base substitution C G downstream_gene_variant PACA-AU 17 26671428 26671428 single base substitution C G exon_variant PACA-AU 17 26671428 26671428 single base substitution C G synonymous_variant L147L 441C>G PACA-AU 17 26671428 26671428 single base substitution C G synonymous_variant L251L 753C>G PACA-CA 17 26663758 26663758 single base substitution C T intron_variant PACA-CA 17 26663758 26663758 single base substitution C T upstream_gene_variant PACA-CA 17 26668169 26668169 single base substitution C T downstream_gene_variant PACA-CA 17 26668169 26668169 single base substitution C T intron_variant PACA-CA 17 26669328 26669328 single base substitution C T downstream_gene_variant PACA-CA 17 26669328 26669328 single base substitution C T exon_variant PACA-CA 17 26669328 26669328 single base substitution C T missense_variant R192C 574C>T PACA-CA 17 26669328 26669328 single base substitution C T missense_variant R88C 262C>T PACA-CA 17 26676415 26676415 single base substitution T C downstream_gene_variant PACA-CA 17 26678462 26678462 single base substitution G T downstream_gene_variant PACA-CA 17 26678756 26678756 single base substitution G A downstream_gene_variant PAEN-AU 17 26669562 26669562 single base substitution C T downstream_gene_variant PAEN-AU 17 26669562 26669562 single base substitution C T intron_variant PBCA-DE 17 26660957 26660957 insertion of <=200bp - A upstream_gene_variant PBCA-DE 17 26661444 26661444 single base substitution A G upstream_gene_variant PBCA-DE 17 26668794 26668794 single base substitution T C downstream_gene_variant PBCA-DE 17 26668794 26668794 single base substitution T C intron_variant PBCA-DE 17 26668986 26668986 single base substitution C A downstream_gene_variant PBCA-DE 17 26668986 26668986 single base substitution C A intron_variant PBCA-DE 17 26672812 26672812 single base substitution C T 3_prime_UTR_variant PBCA-DE 17 26672812 26672812 single base substitution C T downstream_gene_variant PRAD-CA 17 26661730 26661730 single base substitution T C upstream_gene_variant PRAD-CA 17 26668943 26668943 single base substitution C T downstream_gene_variant PRAD-CA 17 26668943 26668943 single base substitution C T intron_variant PRAD-CA 17 26673241 26673241 single base substitution A G 3_prime_UTR_variant PRAD-CA 17 26673241 26673241 single base substitution A G downstream_gene_variant PRAD-UK 17 26658828 26658828 single base substitution G A upstream_gene_variant PRAD-UK 17 26661285 26661285 single base substitution G C upstream_gene_variant PRAD-US 17 26666643 26666643 single base substitution C A intron_variant PRAD-US 17 26666643 26666643 single base substitution C A synonymous_variant L32L 96C>A PRAD-US 17 26666643 26666643 single base substitution C A upstream_gene_variant RECA-EU 17 26674236 26674236 single base substitution T G downstream_gene_variant SKCA-BR 17 26659340 26659340 single base substitution C T upstream_gene_variant SKCA-BR 17 26664374 26664374 single base substitution T C intron_variant SKCA-BR 17 26664374 26664374 single base substitution T C upstream_gene_variant SKCA-BR 17 26667038 26667038 single base substitution T G intron_variant SKCA-BR 17 26667038 26667038 single base substitution T G upstream_gene_variant SKCA-BR 17 26670568 26670568 single base substitution T G downstream_gene_variant SKCA-BR 17 26670568 26670568 single base substitution T G intron_variant SKCA-BR 17 26670576 26670576 single base substitution A G downstream_gene_variant SKCA-BR 17 26670576 26670576 single base substitution A G intron_variant SKCA-BR 17 26676950 26676950 single base substitution C T downstream_gene_variant SKCM-US 17 26659002 26659002 single base substitution C T upstream_gene_variant SKCM-US 17 26666622 26666622 single base substitution G A intron_variant SKCM-US 17 26666622 26666622 single base substitution G A synonymous_variant L25L 75G>A SKCM-US 17 26666622 26666622 single base substitution G A upstream_gene_variant SKCM-US 17 26667480 26667480 single base substitution G A downstream_gene_variant SKCM-US 17 26667480 26667480 single base substitution G A intron_variant SKCM-US 17 26667480 26667480 single base substitution G A synonymous_variant V117V 351G>A SKCM-US 17 26667480 26667480 single base substitution G A synonymous_variant V13V 39G>A SKCM-US 17 26669304 26669304 single base substitution G A downstream_gene_variant SKCM-US 17 26669304 26669304 single base substitution G A exon_variant SKCM-US 17 26669304 26669304 single base substitution G A missense_variant E184K 550G>A SKCM-US 17 26669304 26669304 single base substitution G A missense_variant E80K 238G>A SKCM-US 17 26669339 26669339 single base substitution C T downstream_gene_variant SKCM-US 17 26669339 26669339 single base substitution C T exon_variant SKCM-US 17 26669339 26669339 single base substitution C T synonymous_variant G195G 585C>T SKCM-US 17 26669339 26669339 single base substitution C T synonymous_variant G91G 273C>T SKCM-US 17 26671537 26671537 single base substitution C T downstream_gene_variant SKCM-US 17 26671537 26671537 single base substitution C T synonymous_variant L184L 550C>T SKCM-US 17 26671537 26671537 single base substitution C T synonymous_variant L288L 862C>T STAD-US 17 26666694 26666694 single base substitution C T intron_variant STAD-US 17 26666694 26666694 single base substitution C T synonymous_variant H49H 147C>T STAD-US 17 26666694 26666694 single base substitution C T upstream_gene_variant STAD-US 17 26667474 26667474 single base substitution G A downstream_gene_variant STAD-US 17 26667474 26667474 single base substitution G A intron_variant STAD-US 17 26667474 26667474 single base substitution G A synonymous_variant G115G 345G>A STAD-US 17 26667474 26667474 single base substitution G A synonymous_variant G11G 33G>A STAD-US 17 26669336 26669336 single base substitution C T downstream_gene_variant STAD-US 17 26669336 26669336 single base substitution C T exon_variant STAD-US 17 26669336 26669336 single base substitution C T synonymous_variant N194N 582C>T STAD-US 17 26669336 26669336 single base substitution C T synonymous_variant N90N 270C>T STAD-US 17 26669397 26669397 single base substitution G A downstream_gene_variant STAD-US 17 26669397 26669397 single base substitution G A exon_variant STAD-US 17 26669397 26669397 single base substitution G A missense_variant G111S 331G>A STAD-US 17 26669397 26669397 single base substitution G A missense_variant G215S 643G>A STAD-US 17 26671447 26671447 single base substitution A T downstream_gene_variant STAD-US 17 26671447 26671447 single base substitution A T exon_variant STAD-US 17 26671447 26671447 single base substitution A T missense_variant T154S 460A>T STAD-US 17 26671447 26671447 single base substitution A T missense_variant T258S 772A>T STAD-US 17 26671481 26671481 single base substitution C T downstream_gene_variant STAD-US 17 26671481 26671481 single base substitution C T exon_variant STAD-US 17 26671481 26671481 single base substitution C T missense_variant A165V 494C>T STAD-US 17 26671481 26671481 single base substitution C T missense_variant A269V 806C>T STAD-US 17 26671585 26671585 single base substitution G A downstream_gene_variant STAD-US 17 26671585 26671585 single base substitution G A missense_variant D200N 598G>A STAD-US 17 26671585 26671585 single base substitution G A missense_variant D304N 910G>A STAD-US 17 26675234 26675234 single base substitution G C downstream_gene_variant STAD-US 17 26676190 26676190 single base substitution T G downstream_gene_variant UCEC-US 17 26666726 26666726 single base substitution G A intron_variant UCEC-US 17 26666726 26666726 single base substitution G A missense_variant R60H 179G>A UCEC-US 17 26666726 26666726 single base substitution G A upstream_gene_variant UCEC-US 17 26667447 26667447 single base substitution T G intron_variant UCEC-US 17 26667447 26667447 single base substitution T G synonymous_variant A106A 318T>G UCEC-US 17 26667447 26667447 single base substitution T G synonymous_variant A2A 6T>G UCEC-US 17 26668262 26668262 single base substitution G T downstream_gene_variant UCEC-US 17 26668262 26668262 single base substitution G T splice_acceptor_variant UCEC-US 17 26668329 26668329 single base substitution C T downstream_gene_variant UCEC-US 17 26668329 26668329 single base substitution C T exon_variant UCEC-US 17 26668329 26668329 single base substitution C T missense_variant R148W 442C>T UCEC-US 17 26668329 26668329 single base substitution C T missense_variant R44W 130C>T UCEC-US 17 26675217 26675217 single base substitution C G downstream_gene_variant UCEC-US 17 26677487 26677487 single base substitution G A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESCC_BICR_024T COSM5440881 c.327G>T p.K109N Substitution - Missense 17:28340430-28340430 + 2334199 COSM323900 c.682A>G p.I228V Substitution - Missense 17:28342410-28342410 + T2950 COSM4734844 c.287A>G p.Q96R Substitution - Missense 17:28340390-28340390 + ESCC-003T COSM3937296 c.451G>A p.E151K Substitution - Missense 17:28341312-28341312 + PR-00-1165 COSM247919 c.262C>T p.R88* Substitution - Nonsense 17:28340365-28340365 + TCGA-BR-8591-01 COSM4064884 c.643G>A p.G215S Substitution - Missense 17:28342371-28342371 + TCGA-B8-4620-01 COSM472461 c.273C>T p.T91T Substitution - coding silent 17:28340376-28340376 + NOKSI COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + CHEWS021 COSM4579538 c.800T>C p.L267S Substitution - Missense 17:28344449-28344449 + PT38 COSM5923245 c.697G>A p.E233K Substitution - Missense 17:28342425-28342425 + YUROG COSM3937295 c.433G>A p.E145K Substitution - Missense 17:28341294-28341294 + Au10 COSM5598884 c.450C>T p.I150I Substitution - coding silent 17:28341311-28341311 + TCGA-B5-A11E-01 COSM976845 c.318T>G p.A106A Substitution - coding silent 17:28340421-28340421 + I2L-P7-Tumor-Organoid COSM5363875 c.847_849delGAG p.E284delE Deletion - In frame 17:28344496-28344498 + TCGA-CZ-4854-01 COSM3362038 c.629G>A p.C210Y Substitution - Missense 17:28342357-28342357 + WSU-HN13 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + CRC-02T COSM5454524 c.627C>T p.C209C Substitution - coding silent 17:28342355-28342355 + ESCC-015T COSM3937295 c.433G>A p.E145K Substitution - Missense 17:28341294-28341294 + TCGA-AC-A2FM-01 COSM3819089 c.734G>A p.R245Q Substitution - Missense 17:28344383-28344383 + WSU-HN12 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + 44_T COSM3958129 c.816T>C p.R272R Substitution - coding silent 17:28344465-28344465 + TCGA-ER-A194-01 COSM3515318 c.351G>A p.V117V Substitution - coding silent 17:28340454-28340454 + LIM2551 COSM4644051 c.195C>T p.T65T Substitution - coding silent 17:28339716-28339716 + pfg016T COSM1640616 c.356T>C p.M119T Substitution - Missense 17:28340459-28340459 + SCC-15 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + TCGA-AD-6888-01 COSM1381632 c.469G>A p.V157M Substitution - Missense 17:28341407-28341407 + SCC-25 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + WSU-HN8 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + SNU-175 COSM2800042 c.672C>T p.C224C Substitution - coding silent 17:28342400-28342400 + 8061103 COSM3771294 c.753C>G p.L251L Substitution - coding silent 17:28344402-28344402 + SW403 COSM4264986 c.179G>T p.R60L Substitution - Missense 17:28339700-28339700 + TCGA-BR-8078-01 COSM4064881 c.147C>T p.H49H Substitution - coding silent 17:28339668-28339668 + PCSI_0083_Pa_P_526 COSM3787289 c.574C>T p.R192C Substitution - Missense 17:28342302-28342302 + BICR_22 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + CSCC-45-T COSM4503296 c.636C>T p.S212S Substitution - coding silent 17:28342364-28342364 + 8016470 COSM3387758 c.63G>T p.K21N Substitution - Missense 17:28339584-28339584 + TCGA-19-5959-01 COSM3402682 c.175G>A p.G59R Substitution - Missense 17:28339696-28339696 + YUMOBER COSM5385886 c.700A>C p.K234Q Substitution - Missense 17:28342428-28342428 + CAL33 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + 585223 COSM326706 c.1A>T p.M1L Substitution - Missense 17:28339522-28339522 + 587284 COSM1229860 c.814C>T p.R272C Substitution - Missense 17:28344463-28344463 + TCGA-D1-A17L-01 COSM976847 c.442C>T p.R148W Substitution - Missense 17:28341303-28341303 + 587226 COSM1229859 c.910G>A p.D304N Substitution - Missense 17:28344559-28344559 + TCGA-FS-A1ZW-06 COSM3515319 c.862C>T p.L288L Substitution - coding silent 17:28344511-28344511 + TCGA-AG-A002-01 COSM264109 c.549C>T p.I183I Substitution - coding silent 17:28342277-28342277 + UM-SCC-47 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + CSCC-18-T COSM4447346 c.519-3C>T p.? Unknown 17:28342244-28342244 + TCGA-AA-A010-01 COSM285839 c.550G>A p.E184K Substitution - Missense 17:28342278-28342278 + WSU-HN12 COSM4601192 c.133G>C p.A45P Substitution - Missense 17:28339654-28339654 + S00825 COSM5659123 c.148G>C p.D50H Substitution - Missense 17:28339669-28339669 + TCGA-HU-A4H3-01 COSM4064886 c.806C>T p.A269V Substitution - Missense 17:28344455-28344455 + TCGA-ER-A19W-06 COSM4399038 c.585C>T p.G195G Substitution - coding silent 17:28342313-28342313 + SCC-9 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + TCGA-D1-A17D-01 COSM976846 c.376-1G>T p.? Unknown 17:28341236-28341236 + BD57T COSM5510891 c.878G>A p.R293H Substitution - Missense 17:28344527-28344527 + PD24209a COSM5781006 c.859G>C p.E287Q Substitution - Missense 17:28344508-28344508 + TCGA-CG-5721-01 COSM1229859 c.910G>A p.D304N Substitution - Missense 17:28344559-28344559 + LUAD-NYU282 COSM372420 c.103G>T p.G35C Substitution - Missense 17:28339624-28339624 + TCGA-BR-7197-01 COSM4064885 c.772A>T p.T258S Substitution - Missense 17:28344421-28344421 + 169 COSM3728701 c.669G>A p.V223V Substitution - coding silent 17:28342397-28342397 + TCGA-BS-A0V6-01 COSM976848 c.678C>T p.T226T Substitution - coding silent 17:28342406-28342406 + TCGA-KK-A6E7-01 COSM4876527 c.96C>A p.L32L Substitution - coding silent 17:28339617-28339617 + TCGA-GC-A3OO-01 COSM3787289 c.574C>T p.R192C Substitution - Missense 17:28342302-28342302 + ESCC-249T COSM3937297 c.787G>A p.D263N Substitution - Missense 17:28344436-28344436 + TCGA-GN-A26C-01 COSM3515317 c.75G>A p.L25L Substitution - coding silent 17:28339596-28339596 + WSU-HN30 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + 93VU147T COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + TCGA-AP-A051-01 COSM976844 c.179G>A p.R60H Substitution - Missense 17:28339700-28339700 + TCGA-DA-A1I5-06 COSM285839 c.550G>A p.E184K Substitution - Missense 17:28342278-28342278 + SC_9035 COSM5558445 c.347T>C p.L116P Substitution - Missense 17:28340450-28340450 + Au4 COSM5605153 c.849G>A p.E283E Substitution - coding silent 17:28344498-28344498 + TCGA-BR-4370-01 COSM4064883 c.582C>T p.N194N Substitution - coding silent 17:28342310-28342310 + TARGET-30-PASAAN COSM1288530 c.489C>A p.N163K Substitution - Missense 17:28341427-28341427 + 39 COSM5733823 c.925G>A p.G309S Substitution - Missense 17:28344574-28344574 + BHY COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + UM-SCC-2 COSM4590118 c.139A>C p.T47P Substitution - Missense 17:28339660-28339660 + TCGA-BR-8297-01 COSM4064882 c.345G>A p.G115G Substitution - coding silent 17:28340448-28340448 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.76090 17q22-q23 191161 2450106|CGAP|BC001643|C/T|non-coding||1545|Candidate; 2450106|CGAP|BC001949|C/T|non-coding||1545|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G IntronicSNV . c.518+46A>G 17 26668528 NSCLC A G Missense p.I228V c.682A>G 17 26669436 SCLC A T CdsStartSNV . c.1A>T 17 26666548 SCLC C A Missense p.N163K c.489C>A 17 26668453 NB C A Synonymous p.L32L c.96C>A 17 26666643 PRAD C G Missense p.S175C c.524C>G 17 26669278 HNSC C T 3-UTRSNV . c.948+1189C>T 17 26672812 MB C T Missense p.R148W c.442C>T 17 26668329 UCEC C T Missense p.S2L c.5C>T 17 26666552 HNSC C T Synonymous p.L288L c.862C>T 17 26671537 CM C T Synonymous p.N194N c.582C>T 17 26669336 STAD C T Synonymous p.T91T c.273C>T 17 26667402 RCCC G A 3-UTRSNV . c.948+810G>A 17 26672433 HC G A Missense p.C210Y c.629G>A 17 26669383 RCCC G A Missense p.D129N c.385G>A 17 26668272 CM G A Missense p.E184K c.550G>A 17 26669304 CM G A Missense p.G59R c.175G>A 17 26666722 GBM G A Missense p.R148Q c.443G>A 17 26668330 CM G A Synonymous p.L25L c.75G>A 17 26666622 CM G A Synonymous p.V117V c.351G>A 17 26667480 CM G T SpliceAcceptorSNV . c.376-1G>T 17 26668262 UCEC T C Missense p.M119T c.356T>C 17 26667485 STAD TG GT Missense p.L25C c.74_75delinsGT 17 26666621 CM