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 9 34088357 34088357 + Silent SNP G G T TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr9:34088357G>T c.1353C>A c.(1351-1353)ctC>ctA p.L451L BLCA 9 34088385 34088385 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr9:34088385G>A c.1325C>T c.(1324-1326)tCa>tTa p.S442L BLCA 9 34088417 34088417 + Silent SNP C C T TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr9:34088417C>T c.1293G>A c.(1291-1293)acG>acA p.T431T BLCA 9 34098449 34098449 + Missense_Mutation SNP C C T TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr9:34098449C>T c.668G>A c.(667-669)aGa>aAa p.R223K BLCA 9 34107359 34107359 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr9:34107359C>T c.538G>A c.(538-540)Gat>Aat p.D180N BLCA 9 34107382 34107382 + Missense_Mutation SNP G G T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr9:34107382G>T c.515C>A c.(514-516)aCg>aAg p.T172K BLCA 9 34107398 34107398 + Missense_Mutation SNP T T C TCGA-CF-A3MF-01A-12D-A21A-08 TCGA-CF-A3MF-10A-01D-A21A-08 g.chr9:34107398T>C c.499A>G c.(499-501)Atc>Gtc p.I167V BLCA 9 34107456 34107456 + Missense_Mutation SNP C C G TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr9:34107456C>G c.441G>C c.(439-441)gaG>gaC p.E147D BLCA 9 34107461 34107461 + Missense_Mutation SNP T T C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr9:34107461T>C c.436A>G c.(436-438)Atc>Gtc p.I146V BLCA 9 34125056 34125056 + Missense_Mutation SNP G G C TCGA-YC-A8S6-01A-31D-A38G-08 TCGA-YC-A8S6-10A-01D-A38J-08 g.chr9:34125056G>C c.298C>G c.(298-300)Cat>Gat p.H100D BLCA 9 34125197 34125197 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr9:34125197G>A c.157C>T c.(157-159)Cgg>Tgg p.R53W BLCA 9 34125208 34125208 + Missense_Mutation SNP T T A TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr9:34125208T>A c.146A>T c.(145-147)tAc>tTc p.Y49F BLCA 9 34125217 34125217 + Missense_Mutation SNP A A G TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr9:34125217A>G c.137T>C c.(136-138)tTa>tCa p.L46S BLCA 9 34126363 34126363 + Nonsense_Mutation SNP G G A TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr9:34126363G>A c.67C>T c.(67-69)Cag>Tag p.Q23* BLCA 9 34126369 34126369 + Missense_Mutation SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr9:34126369C>T c.61G>A c.(61-63)Gac>Aac p.D21N BRCA 9 34093425 34093425 + Missense_Mutation SNP A A G TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:34093425A>G c.883T>C c.(883-885)Tat>Cat p.Y295H BRCA 9 34125207 34125207 + Silent SNP G G A TCGA-A2-A3Y0-01A-11D-A23C-09 TCGA-A2-A3Y0-10A-01D-A23C-09 g.chr9:34125207G>A c.147C>T c.(145-147)taC>taT p.Y49Y BRCA 9 34125232 34125232 + Missense_Mutation SNP G G A TCGA-AO-A12D-01A-11D-A10Y-09 TCGA-AO-A12D-10A-01D-A110-09 g.chr9:34125232G>A c.122C>T c.(121-123)cCt>cTt p.P41L COAD 9 34088426 34088426 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:34088426C>T c.1284G>A c.(1282-1284)tcG>tcA p.S428S COAD 9 34098321 34098321 + Splice_Site SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:34098321C>T c.e5+1 COAD 9 34098342 34098342 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:34098342C>T c.775G>A c.(775-777)Gcc>Acc p.A259T COAD 9 34098471 34098473 + In_Frame_Del DEL CAT CAT - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr9:34098471_34098473delCAT c.644_646delATG c.(643-648)gatgtt>gtt p.D215del COAD 9 34107504 34107504 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:34107504C>T c.393G>A c.(391-393)cgG>cgA p.R131R COAD 9 34125223 34125223 + Missense_Mutation SNP C C T TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr9:34125223C>T c.131G>A c.(130-132)aGa>aAa p.R44K COADREAD 9 34088426 34088426 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:34088426C>T c.1284G>A c.(1282-1284)tcG>tcA p.S428S COADREAD 9 34098321 34098321 + Splice_Site SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:34098321C>T c.e5+1 COADREAD 9 34098342 34098342 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:34098342C>T c.775G>A c.(775-777)Gcc>Acc p.A259T COADREAD 9 34098471 34098473 + In_Frame_Del DEL CAT CAT - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr9:34098471_34098473delCAT c.644_646delATG c.(643-648)gatgtt>gtt p.D215del COADREAD 9 34107504 34107504 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:34107504C>T c.393G>A c.(391-393)cgG>cgA p.R131R COADREAD 9 34125223 34125223 + Missense_Mutation SNP C C T TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr9:34125223C>T c.131G>A c.(130-132)aGa>aAa p.R44K COADREAD 9 34125241 34125241 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:34125241C>A c.113G>T c.(112-114)aGa>aTa p.R38I DLBC 9 34125210 34125210 + Silent SNP G G A TCGA-VB-A8QN-01A-11D-A382-10 TCGA-VB-A8QN-10A-01D-A385-10 g.chr9:34125210G>A c.144C>T c.(142-144)taC>taT p.Y48Y ESCA 9 34089557 34089557 + Silent SNP G G T TCGA-IG-A625-01A-11D-A31U-09 TCGA-IG-A625-10A-01D-A31U-09 g.chr9:34089557G>T c.1056C>A c.(1054-1056)atC>atA p.I352I ESCA 9 34093300 34093301 + Missense_Mutation DNP GG GG TA TCGA-IG-A3QL-01A-11D-A247-09 TCGA-IG-A3QL-10A-01D-A247-09 g.chr9:34093300_34093301GG>TA c.1007_1008CC>TA c.(1006-1008)tCC>tTA p.S336L ESCA 9 34125063 34125063 + Missense_Mutation SNP C C A TCGA-L5-A8NL-01A-12D-A37C-09 TCGA-L5-A8NL-11A-12D-A37F-09 g.chr9:34125063C>A c.291G>T c.(289-291)tgG>tgT p.W97C HNSC 9 34093292 34093292 + Missense_Mutation SNP C C T TCGA-P3-A6T4-01A-11D-A34J-08 TCGA-P3-A6T4-10A-01D-A34M-08 g.chr9:34093292C>T c.1016G>A c.(1015-1017)cGa>cAa p.R339Q HNSC 9 34098412 34098412 + Missense_Mutation SNP G G C TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr9:34098412G>C c.705C>G c.(703-705)atC>atG p.I235M HNSC 9 34107381 34107381 + Silent SNP C C A TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr9:34107381C>A c.516G>T c.(514-516)acG>acT p.T172T HNSC 9 34107496 34107496 + Missense_Mutation SNP C C G TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr9:34107496C>G c.401G>C c.(400-402)gGa>gCa p.G134A HNSC 9 34125196 34125196 + Missense_Mutation SNP C C G TCGA-HD-7229-01A-11D-2012-08 TCGA-HD-7229-10A-01D-2013-08 g.chr9:34125196C>G c.158G>C c.(157-159)cGg>cCg p.R53P LIHC 9 34089528 34089528 + Missense_Mutation SNP A A G TCGA-RG-A7D4-01A-12D-A33Q-10 TCGA-RG-A7D4-10A-01D-A33Q-10 g.chr9:34089528A>G c.1085T>C c.(1084-1086)cTg>cCg p.L362P LUAD 9 34089569 34089569 + Silent SNP G G A TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr9:34089569G>A c.1044C>T c.(1042-1044)ttC>ttT p.F348F LUAD 9 34093435 34093435 + Silent SNP G G T TCGA-75-6205-01A-11D-1753-08 TCGA-75-6205-10A-01D-1753-08 g.chr9:34093435G>T c.873C>A c.(871-873)acC>acA p.T291T LUAD 9 34098434 34098434 + Missense_Mutation SNP C C G TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr9:34098434C>G c.683G>C c.(682-684)cGg>cCg p.R228P LUAD 9 34107400 34107400 + Missense_Mutation SNP G G T TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chr9:34107400G>T c.497C>A c.(496-498)gCc>gAc p.A166D LUAD 9 34107422 34107422 + Missense_Mutation SNP C C T TCGA-55-A48Y-01A-11D-A24D-08 TCGA-55-A48Y-10A-01D-A24F-08 g.chr9:34107422C>T c.475G>A c.(475-477)Gga>Aga p.G159R LUAD 9 34125044 34125044 + Missense_Mutation SNP C C A TCGA-17-Z013-01A-01W-0746-08 TCGA-17-Z013-11A-01W-0746-08 g.chr9:34125044C>A c.310G>T c.(310-312)Gtg>Ttg p.V104L LUAD 9 34125082 34125084 + In_Frame_Del DEL TTA TTA - TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr9:34125082_34125084delTTA c.270_272delTAA c.(268-273)aataaa>aaa p.N90del LUAD 9 34125105 34125106 + Frame_Shift_Del DEL CT CT - TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr9:34125105_34125106delCT c.248_249delAG c.(247-249)gagfs p.E83fs LUAD 9 34126386 34126386 + Missense_Mutation SNP G G A TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr9:34126386G>A c.44C>T c.(43-45)tCg>tTg p.S15L LUSC 9 34098402 34098402 + Missense_Mutation SNP C C A TCGA-22-4593-01A-21D-1817-08 TCGA-22-4593-11A-01D-1817-08 g.chr9:34098402C>A c.715G>T c.(715-717)Gcc>Tcc p.A239S READ 9 34125241 34125241 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:34125241C>A c.113G>T c.(112-114)aGa>aTa p.R38I SARC 9 34098374 34098374 + Missense_Mutation SNP G G A TCGA-3B-A9HT-01A-11D-A38Z-09 TCGA-3B-A9HT-10A-01D-A38Z-09 g.chr9:34098374G>A c.743C>T c.(742-744)aCa>aTa p.T248I SKCM 9 34096763 34096763 + Missense_Mutation SNP G G A TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr9:34096763G>A c.812C>T c.(811-813)tCt>tTt p.S271F SKCM 9 34107373 34107373 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr9:34107373G>A c.524C>T c.(523-525)cCt>cTt p.P175L SKCM 9 34125095 34125095 + Missense_Mutation SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr9:34125095C>A c.259G>T c.(259-261)Ggg>Tgg p.G87W

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 34096731 34096731 single base substitution C T downstream_gene_variant BLCA-CN 9 34096731 34096731 single base substitution C T missense_variant E282K 844G>A BLCA-CN 9 34096731 34096731 single base substitution C T upstream_gene_variant BLCA-CN 9 34096751 34096751 single base substitution T C downstream_gene_variant BLCA-CN 9 34096751 34096751 single base substitution T C missense_variant Y275C 824A>G BLCA-CN 9 34096751 34096751 single base substitution T C upstream_gene_variant BLCA-CN 9 34107528 34107528 single base substitution G C exon_variant BLCA-CN 9 34107528 34107528 single base substitution G C synonymous_variant T102T 306C>G BLCA-CN 9 34107528 34107528 single base substitution G C synonymous_variant T105T 315C>G BLCA-CN 9 34107528 34107528 single base substitution G C synonymous_variant T123T 369C>G BLCA-CN 9 34125204 34125204 single base substitution C T exon_variant BLCA-CN 9 34125204 34125204 single base substitution C T synonymous_variant L29L 87G>A BLCA-CN 9 34125204 34125204 single base substitution C T synonymous_variant L32L 96G>A BLCA-CN 9 34125204 34125204 single base substitution C T synonymous_variant L50L 150G>A BLCA-CN 9 34125213 34125213 single base substitution T C exon_variant BLCA-CN 9 34125213 34125213 single base substitution T C synonymous_variant V26V 78A>G BLCA-CN 9 34125213 34125213 single base substitution T C synonymous_variant V29V 87A>G BLCA-CN 9 34125213 34125213 single base substitution T C synonymous_variant V47V 141A>G BLCA-US 9 34107359 34107359 single base substitution C T exon_variant BLCA-US 9 34107359 34107359 single base substitution C T missense_variant D159N 475G>A BLCA-US 9 34107359 34107359 single base substitution C T missense_variant D162N 484G>A BLCA-US 9 34107359 34107359 single base substitution C T missense_variant D180N 538G>A BLCA-US 9 34107398 34107398 single base substitution T C exon_variant BLCA-US 9 34107398 34107398 single base substitution T C missense_variant I146V 436A>G BLCA-US 9 34107398 34107398 single base substitution T C missense_variant I149V 445A>G BLCA-US 9 34107398 34107398 single base substitution T C missense_variant I167V 499A>G BLCA-US 9 34125197 34125197 single base substitution G A exon_variant BLCA-US 9 34125197 34125197 single base substitution G A missense_variant R32W 94C>T BLCA-US 9 34125197 34125197 single base substitution G A missense_variant R35W 103C>T BLCA-US 9 34125197 34125197 single base substitution G A missense_variant R53W 157C>T BLCA-US 9 34125208 34125208 single base substitution T A exon_variant BLCA-US 9 34125208 34125208 single base substitution T A missense_variant Y28F 83A>T BLCA-US 9 34125208 34125208 single base substitution T A missense_variant Y31F 92A>T BLCA-US 9 34125208 34125208 single base substitution T A missense_variant Y49F 146A>T BRCA-EU 9 34082585 34082585 single base substitution G C downstream_gene_variant BRCA-EU 9 34082833 34082833 single base substitution G A downstream_gene_variant BRCA-EU 9 34083015 34083015 single base substitution T A downstream_gene_variant BRCA-EU 9 34084280 34084280 single base substitution G A downstream_gene_variant BRCA-EU 9 34084583 34084583 single base substitution G C downstream_gene_variant BRCA-EU 9 34085771 34085771 single base substitution C A downstream_gene_variant BRCA-EU 9 34087204 34087204 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 34087204 34087204 single base substitution G A downstream_gene_variant BRCA-EU 9 34088621 34088621 single base substitution C T downstream_gene_variant BRCA-EU 9 34088621 34088621 single base substitution C T intron_variant BRCA-EU 9 34089581 34089581 single base substitution C T exon_variant BRCA-EU 9 34089581 34089581 single base substitution C T synonymous_variant R344R 1032G>A BRCA-EU 9 34090481 34090481 single base substitution C G intron_variant BRCA-EU 9 34091232 34091232 single base substitution G A intron_variant BRCA-EU 9 34092462 34092462 single base substitution G A intron_variant BRCA-EU 9 34093098 34093098 single base substitution C T intron_variant BRCA-EU 9 34093149 34093149 single base substitution C T intron_variant BRCA-EU 9 34095028 34095028 single base substitution A T downstream_gene_variant BRCA-EU 9 34095028 34095028 single base substitution A T intron_variant BRCA-EU 9 34095028 34095028 single base substitution A T upstream_gene_variant BRCA-EU 9 34096761 34096761 single base substitution G A downstream_gene_variant BRCA-EU 9 34096761 34096761 single base substitution G A synonymous_variant L272L 814C>T BRCA-EU 9 34096761 34096761 single base substitution G A upstream_gene_variant BRCA-EU 9 34097897 34097897 single base substitution C A downstream_gene_variant BRCA-EU 9 34097897 34097897 single base substitution C A intron_variant BRCA-EU 9 34097897 34097897 single base substitution C A upstream_gene_variant BRCA-EU 9 34099846 34099846 single base substitution T A intron_variant BRCA-EU 9 34100384 34100384 single base substitution G C intron_variant BRCA-EU 9 34101250 34101250 deletion of <=200bp T - intron_variant BRCA-EU 9 34104237 34104237 single base substitution G A downstream_gene_variant BRCA-EU 9 34104237 34104237 single base substitution G A intron_variant BRCA-EU 9 34105667 34105667 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 34105667 34105667 deletion of <=200bp A - intron_variant BRCA-EU 9 34106040 34106040 single base substitution C A downstream_gene_variant BRCA-EU 9 34106040 34106040 single base substitution C A intron_variant BRCA-EU 9 34107944 34107944 single base substitution A T intron_variant BRCA-EU 9 34108813 34108813 insertion of <=200bp - AA intron_variant BRCA-EU 9 34110159 34110159 single base substitution G A intron_variant BRCA-EU 9 34111373 34111373 single base substitution G A intron_variant BRCA-EU 9 34111447 34111447 single base substitution A C intron_variant BRCA-EU 9 34112329 34112329 single base substitution C A intron_variant BRCA-EU 9 34113522 34113522 single base substitution G C intron_variant BRCA-EU 9 34113557 34113557 single base substitution C T intron_variant BRCA-EU 9 34114876 34114876 single base substitution G A intron_variant BRCA-EU 9 34115090 34115090 single base substitution A T intron_variant BRCA-EU 9 34115238 34115238 single base substitution G C intron_variant BRCA-EU 9 34115619 34115619 single base substitution C T intron_variant BRCA-EU 9 34115856 34115856 single base substitution T G intron_variant BRCA-EU 9 34116581 34116581 single base substitution G A intron_variant BRCA-EU 9 34116841 34116841 single base substitution C T intron_variant BRCA-EU 9 34117906 34117906 single base substitution C G intron_variant BRCA-EU 9 34119075 34119075 single base substitution G A intron_variant BRCA-EU 9 34119077 34119077 single base substitution G A intron_variant BRCA-EU 9 34120562 34120562 deletion of <=200bp G - intron_variant BRCA-EU 9 34120771 34120771 single base substitution G C intron_variant BRCA-EU 9 34121833 34121833 single base substitution C G intron_variant BRCA-EU 9 34123482 34123482 single base substitution G C intron_variant BRCA-EU 9 34124869 34124869 single base substitution G C intron_variant BRCA-EU 9 34125440 34125440 single base substitution C G intron_variant BRCA-EU 9 34125500 34125500 single base substitution G A exon_variant BRCA-EU 9 34125500 34125500 single base substitution G A intron_variant BRCA-EU 9 34125893 34125893 single base substitution T C intron_variant BRCA-EU 9 34125893 34125893 single base substitution T C upstream_gene_variant BRCA-EU 9 34126067 34126067 single base substitution C A intron_variant BRCA-EU 9 34126067 34126067 single base substitution C A upstream_gene_variant BRCA-EU 9 34126798 34126798 single base substitution C G intron_variant BRCA-EU 9 34126798 34126798 single base substitution C G upstream_gene_variant BRCA-EU 9 34126820 34126820 single base substitution C G intron_variant BRCA-EU 9 34126820 34126820 single base substitution C G upstream_gene_variant BRCA-EU 9 34128000 34128000 single base substitution C T upstream_gene_variant BRCA-EU 9 34128624 34128624 single base substitution C G upstream_gene_variant BRCA-EU 9 34129449 34129449 single base substitution C A upstream_gene_variant BRCA-EU 9 34129452 34129452 single base substitution G A upstream_gene_variant BRCA-EU 9 34129574 34129574 single base substitution C T upstream_gene_variant BRCA-EU 9 34129581 34129581 single base substitution G A upstream_gene_variant BRCA-EU 9 34130986 34130986 single base substitution G C upstream_gene_variant BRCA-EU 9 34131447 34131447 single base substitution C T upstream_gene_variant BRCA-EU 9 34131973 34131973 single base substitution G A upstream_gene_variant BRCA-EU 9 34132104 34132104 single base substitution G A upstream_gene_variant BRCA-FR 9 34093149 34093149 single base substitution C T intron_variant BRCA-FR 9 34100384 34100384 single base substitution G C intron_variant BRCA-FR 9 34113522 34113522 single base substitution G C intron_variant BRCA-FR 9 34117270 34117270 single base substitution A T intron_variant BRCA-FR 9 34117906 34117906 single base substitution C G intron_variant BRCA-FR 9 34125500 34125500 single base substitution G A exon_variant BRCA-FR 9 34125500 34125500 single base substitution G A intron_variant BRCA-FR 9 34128789 34128789 single base substitution G A upstream_gene_variant BRCA-UK 9 34084583 34084583 single base substitution G C downstream_gene_variant BRCA-UK 9 34085305 34085305 single base substitution G A downstream_gene_variant BRCA-UK 9 34090907 34090907 single base substitution C T intron_variant BRCA-UK 9 34104237 34104237 single base substitution G A downstream_gene_variant BRCA-UK 9 34104237 34104237 single base substitution G A intron_variant BRCA-UK 9 34113307 34113307 single base substitution C T intron_variant BRCA-US 9 34093425 34093425 single base substitution A G downstream_gene_variant BRCA-US 9 34093425 34093425 single base substitution A G exon_variant BRCA-US 9 34093425 34093425 single base substitution A G missense_variant Y295H 883T>C BRCA-US 9 34125207 34125207 single base substitution G A exon_variant BRCA-US 9 34125207 34125207 single base substitution G A synonymous_variant Y28Y 84C>T BRCA-US 9 34125207 34125207 single base substitution G A synonymous_variant Y31Y 93C>T BRCA-US 9 34125207 34125207 single base substitution G A synonymous_variant Y49Y 147C>T BRCA-US 9 34125232 34125232 single base substitution G A exon_variant BRCA-US 9 34125232 34125232 single base substitution G A missense_variant P20L 59C>T BRCA-US 9 34125232 34125232 single base substitution G A missense_variant P23L 68C>T BRCA-US 9 34125232 34125232 single base substitution G A missense_variant P41L 122C>T BTCA-JP 9 34088274 34088274 deletion of <=200bp A - 3_prime_UTR_variant BTCA-JP 9 34088274 34088274 deletion of <=200bp A - downstream_gene_variant CLLE-ES 9 34096815 34096815 single base substitution C A downstream_gene_variant CLLE-ES 9 34096815 34096815 single base substitution C A intron_variant CLLE-ES 9 34096815 34096815 single base substitution C A upstream_gene_variant CLLE-ES 9 34110447 34110447 single base substitution T G intron_variant CLLE-ES 9 34114978 34114978 single base substitution C A intron_variant CLLE-ES 9 34119073 34119073 single base substitution T C intron_variant CLLE-ES 9 34119440 34119440 single base substitution T C intron_variant CLLE-ES 9 34120686 34120686 deletion of <=200bp G - intron_variant COAD-US 9 34088426 34088426 single base substitution C T downstream_gene_variant COAD-US 9 34088426 34088426 single base substitution C T synonymous_variant S428S 1284G>A COAD-US 9 34098321 34098321 single base substitution C T downstream_gene_variant COAD-US 9 34098321 34098321 single base substitution C T splice_donor_variant COAD-US 9 34098321 34098321 single base substitution C T upstream_gene_variant COAD-US 9 34098471 34098473 deletion of <=200bp CAT - disruptive_inframe_deletion DV197V COAD-US 9 34098471 34098473 deletion of <=200bp CAT - disruptive_inframe_deletion DV215V COAD-US 9 34098471 34098473 deletion of <=200bp CAT - downstream_gene_variant COAD-US 9 34098471 34098473 deletion of <=200bp CAT - upstream_gene_variant COAD-US 9 34107504 34107504 single base substitution C T exon_variant COAD-US 9 34107504 34107504 single base substitution C T synonymous_variant R110R 330G>A COAD-US 9 34107504 34107504 single base substitution C T synonymous_variant R113R 339G>A COAD-US 9 34107504 34107504 single base substitution C T synonymous_variant R131R 393G>A COAD-US 9 34125223 34125223 single base substitution C T exon_variant COAD-US 9 34125223 34125223 single base substitution C T missense_variant R23K 68G>A COAD-US 9 34125223 34125223 single base substitution C T missense_variant R26K 77G>A COAD-US 9 34125223 34125223 single base substitution C T missense_variant R44K 131G>A COCA-CN 9 34089378 34089378 single base substitution G A downstream_gene_variant COCA-CN 9 34089378 34089378 single base substitution G A intron_variant COCA-CN 9 34097533 34097533 single base substitution C T downstream_gene_variant COCA-CN 9 34097533 34097533 single base substitution C T intron_variant COCA-CN 9 34097533 34097533 single base substitution C T upstream_gene_variant COCA-CN 9 34102676 34102676 single base substitution A C downstream_gene_variant COCA-CN 9 34102676 34102676 single base substitution A C intron_variant COCA-CN 9 34107310 34107310 single base substitution G A downstream_gene_variant COCA-CN 9 34107310 34107310 single base substitution G A intron_variant COCA-CN 9 34108800 34108800 single base substitution T A intron_variant COCA-CN 9 34108810 34108810 single base substitution A T intron_variant COCA-CN 9 34115355 34115355 single base substitution C T intron_variant COCA-CN 9 34128332 34128332 single base substitution T G upstream_gene_variant COCA-CN 9 34128427 34128427 single base substitution C T upstream_gene_variant COCA-CN 9 34132387 34132387 single base substitution T G upstream_gene_variant EOPC-DE 9 34117903 34117903 single base substitution A C intron_variant ESAD-UK 9 34082544 34082544 single base substitution C T downstream_gene_variant ESAD-UK 9 34084267 34084267 single base substitution A C downstream_gene_variant ESAD-UK 9 34084682 34084682 single base substitution A C downstream_gene_variant ESAD-UK 9 34086799 34086799 single base substitution T C 3_prime_UTR_variant ESAD-UK 9 34086799 34086799 single base substitution T C downstream_gene_variant ESAD-UK 9 34087919 34087919 single base substitution A T 3_prime_UTR_variant ESAD-UK 9 34087919 34087919 single base substitution A T downstream_gene_variant ESAD-UK 9 34090952 34090952 single base substitution G A intron_variant ESAD-UK 9 34092142 34092142 single base substitution C T intron_variant ESAD-UK 9 34094170 34094170 single base substitution A C downstream_gene_variant ESAD-UK 9 34094170 34094170 single base substitution A C intron_variant ESAD-UK 9 34094170 34094170 single base substitution A C upstream_gene_variant ESAD-UK 9 34094622 34094622 single base substitution G C downstream_gene_variant ESAD-UK 9 34094622 34094622 single base substitution G C intron_variant ESAD-UK 9 34094622 34094622 single base substitution G C upstream_gene_variant ESAD-UK 9 34096410 34096410 single base substitution A C downstream_gene_variant ESAD-UK 9 34096410 34096410 single base substitution A C intron_variant ESAD-UK 9 34096410 34096410 single base substitution A C upstream_gene_variant ESAD-UK 9 34099211 34099211 single base substitution G A intron_variant ESAD-UK 9 34099333 34099333 single base substitution C T intron_variant ESAD-UK 9 34108507 34108507 single base substitution G T intron_variant ESAD-UK 9 34109903 34109903 single base substitution G A intron_variant ESAD-UK 9 34112884 34112884 single base substitution G A intron_variant ESAD-UK 9 34112926 34112926 single base substitution C G intron_variant ESAD-UK 9 34115145 34115145 single base substitution G A intron_variant ESAD-UK 9 34115606 34115606 single base substitution A C intron_variant ESAD-UK 9 34117135 34117135 single base substitution C T intron_variant ESAD-UK 9 34117321 34117321 single base substitution T A intron_variant ESAD-UK 9 34117795 34117795 single base substitution C T intron_variant ESAD-UK 9 34118631 34118631 single base substitution G A intron_variant ESAD-UK 9 34120300 34120300 single base substitution C T intron_variant ESAD-UK 9 34121377 34121377 single base substitution T A intron_variant ESAD-UK 9 34121421 34121421 single base substitution G A intron_variant ESAD-UK 9 34122038 34122038 single base substitution G A intron_variant ESAD-UK 9 34128241 34128241 single base substitution G A upstream_gene_variant ESAD-UK 9 34128516 34128516 single base substitution C T upstream_gene_variant ESAD-UK 9 34129273 34129273 single base substitution C T upstream_gene_variant ESAD-UK 9 34131209 34131209 single base substitution G A upstream_gene_variant ESAD-UK 9 34132343 34132343 single base substitution G A upstream_gene_variant ESAD-UK 9 34132385 34132385 single base substitution A T upstream_gene_variant ESCA-CN 9 34088701 34088701 single base substitution C T downstream_gene_variant ESCA-CN 9 34088701 34088701 single base substitution C T intron_variant ESCA-CN 9 34093274 34093274 single base substitution G C intron_variant LAML-KR 9 34093371 34093371 single base substitution C A exon_variant LAML-KR 9 34093371 34093371 single base substitution C A missense_variant V313L 937G>T LAML-KR 9 34099100 34099100 single base substitution C T intron_variant LICA-FR 9 34081902 34081902 deletion of <=200bp A - downstream_gene_variant LICA-FR 9 34107483 34107483 single base substitution C T exon_variant LICA-FR 9 34107483 34107483 single base substitution C T synonymous_variant Q117Q 351G>A LICA-FR 9 34107483 34107483 single base substitution C T synonymous_variant Q120Q 360G>A LICA-FR 9 34107483 34107483 single base substitution C T synonymous_variant Q138Q 414G>A LICA-FR 9 34110984 34110984 deletion of <=200bp T - intron_variant LICA-FR 9 34111979 34111979 insertion of <=200bp - AA intron_variant LICA-FR 9 34115668 34115668 single base substitution T C intron_variant LICA-FR 9 34119701 34119702 deletion of <=200bp TT - intron_variant LICA-FR 9 34122472 34122472 deletion of <=200bp T - intron_variant LICA-FR 9 34126363 34126363 single base substitution G T intron_variant LICA-FR 9 34126363 34126363 single base substitution G T missense_variant Q23K 67C>A LICA-FR 9 34126363 34126363 single base substitution G T upstream_gene_variant LIHC-US 9 34089528 34089528 single base substitution A G exon_variant LIHC-US 9 34089528 34089528 single base substitution A G missense_variant L362P 1085T>C LINC-JP 9 34082210 34082210 single base substitution C T downstream_gene_variant LINC-JP 9 34088366 34088367 deletion of <=200bp AT - downstream_gene_variant LINC-JP 9 34088366 34088367 deletion of <=200bp AT - frameshift_variant Y448 LINC-JP 9 34088495 34088495 single base substitution T A downstream_gene_variant LINC-JP 9 34088495 34088495 single base substitution T A missense_variant E405D 1215A>T LINC-JP 9 34089706 34089706 single base substitution C A intron_variant LINC-JP 9 34097355 34097355 single base substitution T C downstream_gene_variant LINC-JP 9 34097355 34097355 single base substitution T C intron_variant LINC-JP 9 34097355 34097355 single base substitution T C upstream_gene_variant LINC-JP 9 34125244 34125244 single base substitution T C exon_variant LINC-JP 9 34125244 34125244 single base substitution T C missense_variant K16R 47A>G LINC-JP 9 34125244 34125244 single base substitution T C missense_variant K19R 56A>G LINC-JP 9 34125244 34125244 single base substitution T C missense_variant K37R 110A>G LINC-JP 9 34126102 34126102 single base substitution C G intron_variant LINC-JP 9 34126102 34126102 single base substitution C G upstream_gene_variant LIRI-JP 9 34081583 34081583 single base substitution G A downstream_gene_variant LIRI-JP 9 34082705 34082705 single base substitution G C downstream_gene_variant LIRI-JP 9 34086985 34086985 single base substitution G C 3_prime_UTR_variant LIRI-JP 9 34086985 34086985 single base substitution G C downstream_gene_variant LIRI-JP 9 34087058 34087058 single base substitution G A 3_prime_UTR_variant LIRI-JP 9 34087058 34087058 single base substitution G A downstream_gene_variant LIRI-JP 9 34087276 34087276 single base substitution T G 3_prime_UTR_variant LIRI-JP 9 34087276 34087276 single base substitution T G downstream_gene_variant LIRI-JP 9 34088886 34088886 single base substitution T C downstream_gene_variant LIRI-JP 9 34088886 34088886 single base substitution T C intron_variant LIRI-JP 9 34088908 34088908 single base substitution G C downstream_gene_variant LIRI-JP 9 34088908 34088908 single base substitution G C intron_variant LIRI-JP 9 34090022 34090022 single base substitution T C intron_variant LIRI-JP 9 34090780 34090780 single base substitution G A intron_variant LIRI-JP 9 34092246 34092246 single base substitution C T intron_variant LIRI-JP 9 34092500 34092500 single base substitution A G intron_variant LIRI-JP 9 34092856 34092856 single base substitution T G intron_variant LIRI-JP 9 34095532 34095532 single base substitution T C downstream_gene_variant LIRI-JP 9 34095532 34095532 single base substitution T C intron_variant LIRI-JP 9 34095532 34095532 single base substitution T C upstream_gene_variant LIRI-JP 9 34095544 34095544 single base substitution T C downstream_gene_variant LIRI-JP 9 34095544 34095544 single base substitution T C intron_variant LIRI-JP 9 34095544 34095544 single base substitution T C upstream_gene_variant LIRI-JP 9 34096609 34096609 single base substitution A T downstream_gene_variant LIRI-JP 9 34096609 34096609 single base substitution A T intron_variant LIRI-JP 9 34096609 34096609 single base substitution A T upstream_gene_variant LIRI-JP 9 34098112 34098112 single base substitution C A downstream_gene_variant LIRI-JP 9 34098112 34098112 single base substitution C A intron_variant LIRI-JP 9 34098112 34098112 single base substitution C A upstream_gene_variant LIRI-JP 9 34100357 34100357 single base substitution T C intron_variant LIRI-JP 9 34101247 34101247 single base substitution T A intron_variant LIRI-JP 9 34103001 34103001 single base substitution T C downstream_gene_variant LIRI-JP 9 34103001 34103001 single base substitution T C intron_variant LIRI-JP 9 34110605 34110605 deletion of <=200bp T - intron_variant LIRI-JP 9 34111465 34111465 single base substitution C A intron_variant LIRI-JP 9 34117133 34117133 single base substitution T A intron_variant LIRI-JP 9 34117470 34117470 single base substitution C G intron_variant LIRI-JP 9 34117653 34117653 single base substitution C T intron_variant LIRI-JP 9 34123517 34123517 single base substitution C G intron_variant LIRI-JP 9 34123885 34123885 single base substitution G C intron_variant LIRI-JP 9 34129957 34129957 single base substitution A C upstream_gene_variant LUSC-KR 9 34083171 34083171 single base substitution G T downstream_gene_variant LUSC-KR 9 34085759 34085759 single base substitution G C downstream_gene_variant LUSC-KR 9 34087360 34087360 single base substitution T C 3_prime_UTR_variant LUSC-KR 9 34087360 34087360 single base substitution T C downstream_gene_variant LUSC-KR 9 34089395 34089395 single base substitution T C downstream_gene_variant LUSC-KR 9 34089395 34089395 single base substitution T C intron_variant LUSC-KR 9 34091375 34091375 single base substitution T A intron_variant LUSC-KR 9 34093274 34093274 single base substitution G C intron_variant LUSC-KR 9 34096597 34096597 single base substitution G A downstream_gene_variant LUSC-KR 9 34096597 34096597 single base substitution G A intron_variant LUSC-KR 9 34096597 34096597 single base substitution G A upstream_gene_variant LUSC-KR 9 34096873 34096873 single base substitution T C downstream_gene_variant LUSC-KR 9 34096873 34096873 single base substitution T C intron_variant LUSC-KR 9 34096873 34096873 single base substitution T C upstream_gene_variant LUSC-KR 9 34105108 34105108 single base substitution T A downstream_gene_variant LUSC-KR 9 34105108 34105108 single base substitution T A intron_variant LUSC-KR 9 34106410 34106410 single base substitution C T downstream_gene_variant LUSC-KR 9 34106410 34106410 single base substitution C T intron_variant LUSC-KR 9 34112485 34112485 single base substitution G A intron_variant LUSC-KR 9 34113022 34113022 single base substitution C T intron_variant LUSC-KR 9 34119378 34119378 single base substitution T A intron_variant LUSC-KR 9 34124513 34124513 single base substitution A G intron_variant LUSC-KR 9 34130977 34130977 single base substitution G C upstream_gene_variant LUSC-US 9 34098402 34098402 single base substitution C A downstream_gene_variant LUSC-US 9 34098402 34098402 single base substitution C A missense_variant A221S 661G>T LUSC-US 9 34098402 34098402 single base substitution C A missense_variant A239S 715G>T LUSC-US 9 34098402 34098402 single base substitution C A upstream_gene_variant MALY-DE 9 34083454 34083454 single base substitution T G downstream_gene_variant MALY-DE 9 34088440 34088440 single base substitution G C downstream_gene_variant MALY-DE 9 34088440 34088440 single base substitution G C missense_variant H424D 1270C>G MALY-DE 9 34091742 34091742 single base substitution A G intron_variant MALY-DE 9 34092180 34092180 single base substitution T C intron_variant MALY-DE 9 34093375 34093375 single base substitution A G exon_variant MALY-DE 9 34093375 34093375 single base substitution A G synonymous_variant Y311Y 933T>C MALY-DE 9 34095371 34095379 deletion of <=200bp TTTTTTTTT - downstream_gene_variant MALY-DE 9 34095371 34095379 deletion of <=200bp TTTTTTTTT - intron_variant MALY-DE 9 34095371 34095379 deletion of <=200bp TTTTTTTTT - upstream_gene_variant MALY-DE 9 34095620 34095620 single base substitution C T downstream_gene_variant MALY-DE 9 34095620 34095620 single base substitution C T intron_variant MALY-DE 9 34095620 34095620 single base substitution C T upstream_gene_variant MALY-DE 9 34100892 34100892 single base substitution C T intron_variant MALY-DE 9 34105780 34105780 insertion of <=200bp - A downstream_gene_variant MALY-DE 9 34105780 34105780 insertion of <=200bp - A intron_variant MALY-DE 9 34110648 34110648 single base substitution G T intron_variant MALY-DE 9 34123349 34123349 single base substitution A G intron_variant MALY-DE 9 34123826 34123826 single base substitution G T intron_variant MELA-AU 9 34082088 34082088 single base substitution C T downstream_gene_variant MELA-AU 9 34082256 34082256 single base substitution C T downstream_gene_variant MELA-AU 9 34083003 34083003 single base substitution C T downstream_gene_variant MELA-AU 9 34083157 34083157 single base substitution T C downstream_gene_variant MELA-AU 9 34084106 34084106 single base substitution C T downstream_gene_variant MELA-AU 9 34084122 34084122 single base substitution A T downstream_gene_variant MELA-AU 9 34084515 34084515 single base substitution G A downstream_gene_variant MELA-AU 9 34085123 34085123 single base substitution C G downstream_gene_variant MELA-AU 9 34085578 34085578 single base substitution C T downstream_gene_variant MELA-AU 9 34086955 34086955 single base substitution G A 3_prime_UTR_variant MELA-AU 9 34086955 34086955 single base substitution G A downstream_gene_variant MELA-AU 9 34087447 34087447 single base substitution G A 3_prime_UTR_variant MELA-AU 9 34087447 34087447 single base substitution G A downstream_gene_variant MELA-AU 9 34088512 34088512 single base substitution G A downstream_gene_variant MELA-AU 9 34088512 34088512 single base substitution G A intron_variant MELA-AU 9 34089398 34089398 single base substitution G A downstream_gene_variant MELA-AU 9 34089398 34089398 single base substitution G A intron_variant MELA-AU 9 34090328 34090328 single base substitution G A intron_variant MELA-AU 9 34090894 34090894 single base substitution G A intron_variant MELA-AU 9 34091642 34091642 single base substitution A T intron_variant MELA-AU 9 34091675 34091675 single base substitution A C intron_variant MELA-AU 9 34092907 34092907 single base substitution G A intron_variant MELA-AU 9 34093573 34093573 single base substitution A C downstream_gene_variant MELA-AU 9 34093573 34093573 single base substitution A C exon_variant MELA-AU 9 34093573 34093573 single base substitution A C intron_variant MELA-AU 9 34094518 34094518 single base substitution G A downstream_gene_variant MELA-AU 9 34094518 34094518 single base substitution G A intron_variant MELA-AU 9 34094518 34094518 single base substitution G A upstream_gene_variant MELA-AU 9 34094741 34094741 single base substitution G A downstream_gene_variant MELA-AU 9 34094741 34094741 single base substitution G A intron_variant MELA-AU 9 34094741 34094741 single base substitution G A upstream_gene_variant MELA-AU 9 34095367 34095367 single base substitution G A downstream_gene_variant MELA-AU 9 34095367 34095367 single base substitution G A intron_variant MELA-AU 9 34095367 34095367 single base substitution G A upstream_gene_variant MELA-AU 9 34095704 34095704 single base substitution G A downstream_gene_variant MELA-AU 9 34095704 34095704 single base substitution G A intron_variant MELA-AU 9 34095704 34095704 single base substitution G A upstream_gene_variant MELA-AU 9 34095823 34095823 single base substitution A G downstream_gene_variant MELA-AU 9 34095823 34095823 single base substitution A G intron_variant MELA-AU 9 34095823 34095823 single base substitution A G upstream_gene_variant MELA-AU 9 34096301 34096301 single base substitution C T downstream_gene_variant MELA-AU 9 34096301 34096301 single base substitution C T intron_variant MELA-AU 9 34096301 34096301 single base substitution C T upstream_gene_variant MELA-AU 9 34097176 34097176 single base substitution G A downstream_gene_variant MELA-AU 9 34097176 34097176 single base substitution G A intron_variant MELA-AU 9 34097176 34097176 single base substitution G A upstream_gene_variant MELA-AU 9 34097857 34097857 single base substitution G A downstream_gene_variant MELA-AU 9 34097857 34097857 single base substitution G A intron_variant MELA-AU 9 34097857 34097857 single base substitution G A upstream_gene_variant MELA-AU 9 34098430 34098430 single base substitution G A downstream_gene_variant MELA-AU 9 34098430 34098430 single base substitution G A synonymous_variant V211V 633C>T MELA-AU 9 34098430 34098430 single base substitution G A synonymous_variant V229V 687C>T MELA-AU 9 34098430 34098430 single base substitution G A upstream_gene_variant MELA-AU 9 34098484 34098484 single base substitution C T downstream_gene_variant MELA-AU 9 34098484 34098484 single base substitution C T synonymous_variant E193E 579G>A MELA-AU 9 34098484 34098484 single base substitution C T synonymous_variant E211E 633G>A MELA-AU 9 34098484 34098484 single base substitution C T upstream_gene_variant MELA-AU 9 34099006 34099006 single base substitution G A intron_variant MELA-AU 9 34099661 34099661 single base substitution G A intron_variant MELA-AU 9 34099972 34099972 single base substitution G A intron_variant MELA-AU 9 34100967 34100967 single base substitution A G intron_variant MELA-AU 9 34101774 34101774 single base substitution A G intron_variant MELA-AU 9 34102545 34102545 single base substitution G A downstream_gene_variant MELA-AU 9 34102545 34102545 single base substitution G A intron_variant MELA-AU 9 34102657 34102657 single base substitution C A downstream_gene_variant MELA-AU 9 34102657 34102657 single base substitution C A intron_variant MELA-AU 9 34103498 34103498 single base substitution G A downstream_gene_variant MELA-AU 9 34103498 34103498 single base substitution G A intron_variant MELA-AU 9 34103866 34103866 single base substitution G A downstream_gene_variant MELA-AU 9 34103866 34103866 single base substitution G A intron_variant MELA-AU 9 34104690 34104690 single base substitution G A downstream_gene_variant MELA-AU 9 34104690 34104690 single base substitution G A intron_variant MELA-AU 9 34105967 34105967 single base substitution C T downstream_gene_variant MELA-AU 9 34105967 34105967 single base substitution C T intron_variant MELA-AU 9 34106824 34106824 single base substitution C A downstream_gene_variant MELA-AU 9 34106824 34106824 single base substitution C A intron_variant MELA-AU 9 34107137 34107137 single base substitution G C downstream_gene_variant MELA-AU 9 34107137 34107137 single base substitution G C intron_variant MELA-AU 9 34107955 34107955 single base substitution G A intron_variant MELA-AU 9 34109705 34109705 single base substitution G A intron_variant MELA-AU 9 34111345 34111345 single base substitution C T intron_variant MELA-AU 9 34111629 34111629 single base substitution G A intron_variant MELA-AU 9 34112884 34112884 single base substitution G A intron_variant MELA-AU 9 34114992 34114992 single base substitution A T intron_variant MELA-AU 9 34115362 34115362 single base substitution G A intron_variant MELA-AU 9 34117102 34117102 single base substitution G A intron_variant MELA-AU 9 34117807 34117807 single base substitution G A intron_variant MELA-AU 9 34119808 34119808 single base substitution T A intron_variant MELA-AU 9 34120127 34120127 single base substitution G A intron_variant MELA-AU 9 34120595 34120595 single base substitution G A intron_variant MELA-AU 9 34120928 34120928 single base substitution G A intron_variant MELA-AU 9 34120944 34120944 single base substitution G A intron_variant MELA-AU 9 34122172 34122172 single base substitution G A intron_variant MELA-AU 9 34122498 34122498 single base substitution G A intron_variant MELA-AU 9 34123021 34123023 deletion of <=200bp CCT - intron_variant MELA-AU 9 34123299 34123299 single base substitution G A intron_variant MELA-AU 9 34123946 34123946 single base substitution G A intron_variant MELA-AU 9 34125903 34125903 single base substitution G A intron_variant MELA-AU 9 34125903 34125903 single base substitution G A upstream_gene_variant MELA-AU 9 34126225 34126225 single base substitution G A intron_variant MELA-AU 9 34126225 34126225 single base substitution G A upstream_gene_variant MELA-AU 9 34126630 34126630 single base substitution G A 5_prime_UTR_variant MELA-AU 9 34126630 34126630 single base substitution G A intron_variant MELA-AU 9 34126630 34126630 single base substitution G A upstream_gene_variant MELA-AU 9 34127326 34127326 single base substitution C T 5_prime_UTR_variant MELA-AU 9 34127326 34127326 single base substitution C T upstream_gene_variant MELA-AU 9 34128162 34128162 single base substitution G A upstream_gene_variant MELA-AU 9 34128242 34128242 single base substitution C G upstream_gene_variant MELA-AU 9 34128312 34128312 single base substitution G A upstream_gene_variant MELA-AU 9 34128507 34128507 single base substitution C T upstream_gene_variant MELA-AU 9 34128727 34128728 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 34129560 34129560 single base substitution G A upstream_gene_variant MELA-AU 9 34130226 34130226 single base substitution G A upstream_gene_variant MELA-AU 9 34130627 34130627 single base substitution C T upstream_gene_variant MELA-AU 9 34130659 34130659 single base substitution C T upstream_gene_variant MELA-AU 9 34130675 34130675 single base substitution C T upstream_gene_variant MELA-AU 9 34131037 34131037 single base substitution C T upstream_gene_variant MELA-AU 9 34131167 34131167 single base substitution G A upstream_gene_variant MELA-AU 9 34131276 34131276 single base substitution G A upstream_gene_variant MELA-AU 9 34131553 34131553 single base substitution G A upstream_gene_variant MELA-AU 9 34131850 34131850 single base substitution G A upstream_gene_variant MELA-AU 9 34131946 34131946 single base substitution G A upstream_gene_variant MELA-AU 9 34132222 34132222 single base substitution G A upstream_gene_variant ORCA-IN 9 34083474 34083474 single base substitution C G downstream_gene_variant ORCA-IN 9 34083583 34083583 single base substitution C G downstream_gene_variant ORCA-IN 9 34084086 34084086 single base substitution C G downstream_gene_variant ORCA-IN 9 34090092 34090092 single base substitution C T intron_variant ORCA-IN 9 34090295 34090295 single base substitution C G intron_variant OV-AU 9 34083058 34083058 single base substitution G A downstream_gene_variant OV-AU 9 34084925 34084925 single base substitution C T downstream_gene_variant OV-AU 9 34097375 34097375 single base substitution C T downstream_gene_variant OV-AU 9 34097375 34097375 single base substitution C T intron_variant OV-AU 9 34097375 34097375 single base substitution C T upstream_gene_variant OV-AU 9 34101814 34101814 single base substitution A G intron_variant OV-AU 9 34105640 34105640 single base substitution T C downstream_gene_variant OV-AU 9 34105640 34105640 single base substitution T C intron_variant OV-AU 9 34118124 34118124 single base substitution C G intron_variant OV-AU 9 34128258 34128258 single base substitution T C upstream_gene_variant OV-AU 9 34130687 34130687 single base substitution G A upstream_gene_variant OV-AU 9 34131264 34131264 single base substitution C A upstream_gene_variant PACA-AU 9 34083159 34083159 single base substitution T C downstream_gene_variant PACA-AU 9 34089002 34089002 single base substitution G A downstream_gene_variant PACA-AU 9 34089002 34089002 single base substitution G A intron_variant PACA-AU 9 34090815 34090815 single base substitution G A intron_variant PACA-AU 9 34095218 34095218 single base substitution G A downstream_gene_variant PACA-AU 9 34095218 34095218 single base substitution G A intron_variant PACA-AU 9 34095218 34095218 single base substitution G A upstream_gene_variant PACA-AU 9 34099602 34099602 deletion of <=200bp T - intron_variant PACA-AU 9 34106487 34106487 single base substitution T C downstream_gene_variant PACA-AU 9 34106487 34106487 single base substitution T C synonymous_variant G161G 483A>G PACA-AU 9 34106487 34106487 single base substitution T C synonymous_variant G164G 492A>G PACA-AU 9 34106487 34106487 single base substitution T C synonymous_variant G182G 546A>G PACA-AU 9 34108982 34108982 single base substitution T A intron_variant PACA-AU 9 34111858 34111858 single base substitution C T intron_variant PACA-AU 9 34122130 34122130 single base substitution C T intron_variant PACA-AU 9 34123186 34123186 single base substitution A G intron_variant PACA-AU 9 34129638 34129638 single base substitution C T upstream_gene_variant PACA-AU 9 34131454 34131454 single base substitution C A upstream_gene_variant PACA-CA 9 34084535 34084535 single base substitution T C downstream_gene_variant PACA-CA 9 34091670 34091672 deletion of <=200bp CCC - intron_variant PACA-CA 9 34092100 34092100 single base substitution T A intron_variant PACA-CA 9 34095838 34095838 deletion of <=200bp C - downstream_gene_variant PACA-CA 9 34095838 34095838 deletion of <=200bp C - intron_variant PACA-CA 9 34095838 34095838 deletion of <=200bp C - upstream_gene_variant PACA-CA 9 34096746 34096746 single base substitution G A downstream_gene_variant PACA-CA 9 34096746 34096746 single base substitution G A missense_variant H277Y 829C>T PACA-CA 9 34096746 34096746 single base substitution G A upstream_gene_variant PACA-CA 9 34106424 34106424 single base substitution A G downstream_gene_variant PACA-CA 9 34106424 34106424 single base substitution A G splice_region_variant PACA-CA 9 34107708 34107708 single base substitution A G intron_variant PACA-CA 9 34113688 34113688 single base substitution C T intron_variant PACA-CA 9 34113734 34113734 single base substitution A G intron_variant PACA-CA 9 34113881 34113881 single base substitution C T intron_variant PACA-CA 9 34114161 34114161 deletion of <=200bp G - intron_variant PACA-CA 9 34117499 34117499 single base substitution G A intron_variant PACA-CA 9 34118037 34118037 single base substitution G A intron_variant PACA-CA 9 34121545 34121545 single base substitution T A intron_variant PACA-CA 9 34128747 34128747 single base substitution G A upstream_gene_variant PAEN-AU 9 34123873 34123873 single base substitution C T intron_variant PAEN-IT 9 34118514 34118514 single base substitution C A intron_variant PAEN-IT 9 34120950 34120950 single base substitution G A intron_variant PAEN-IT 9 34131101 34131101 single base substitution G T upstream_gene_variant PBCA-DE 9 34103319 34103319 single base substitution C T downstream_gene_variant PBCA-DE 9 34103319 34103319 single base substitution C T intron_variant PBCA-DE 9 34115378 34115380 deletion of <=200bp AGG - intron_variant PBCA-DE 9 34115485 34115485 deletion of <=200bp T - intron_variant PBCA-DE 9 34115488 34115488 insertion of <=200bp - T intron_variant PBCA-DE 9 34118470 34118470 single base substitution A G intron_variant PBCA-DE 9 34119015 34119015 single base substitution C T intron_variant PBCA-DE 9 34127093 34127093 single base substitution A G intron_variant PBCA-DE 9 34127093 34127093 single base substitution A G upstream_gene_variant PBCA-DE 9 34128057 34128057 single base substitution G C upstream_gene_variant PBCA-DE 9 34132255 34132255 single base substitution T G upstream_gene_variant PRAD-CA 9 34081396 34081396 single base substitution A T downstream_gene_variant PRAD-CA 9 34093129 34093129 single base substitution A T intron_variant PRAD-CA 9 34099296 34099296 single base substitution G A intron_variant PRAD-CA 9 34128267 34128267 single base substitution G T upstream_gene_variant PRAD-CA 9 34128427 34128427 single base substitution C T upstream_gene_variant PRAD-UK 9 34087918 34087918 insertion of <=200bp - CA 3_prime_UTR_variant PRAD-UK 9 34087918 34087918 insertion of <=200bp - CA downstream_gene_variant PRAD-UK 9 34087930 34087930 insertion of <=200bp - CA 3_prime_UTR_variant PRAD-UK 9 34087930 34087930 insertion of <=200bp - CA downstream_gene_variant PRAD-UK 9 34090666 34090666 deletion of <=200bp T - intron_variant PRAD-UK 9 34098132 34098132 single base substitution A C downstream_gene_variant PRAD-UK 9 34098132 34098132 single base substitution A C intron_variant PRAD-UK 9 34098132 34098132 single base substitution A C upstream_gene_variant PRAD-UK 9 34116987 34116987 single base substitution C T intron_variant PRAD-UK 9 34125509 34125509 single base substitution G A exon_variant PRAD-UK 9 34125509 34125509 single base substitution G A intron_variant PRAD-UK 9 34126273 34126273 single base substitution C T intron_variant PRAD-UK 9 34126273 34126273 single base substitution C T upstream_gene_variant RECA-EU 9 34083839 34083839 single base substitution T C downstream_gene_variant RECA-EU 9 34103784 34103784 single base substitution G A downstream_gene_variant RECA-EU 9 34103784 34103784 single base substitution G A intron_variant RECA-EU 9 34107152 34107152 single base substitution G A downstream_gene_variant RECA-EU 9 34107152 34107152 single base substitution G A intron_variant RECA-EU 9 34119609 34119609 single base substitution C G intron_variant RECA-EU 9 34120156 34120156 single base substitution G A intron_variant RECA-EU 9 34122384 34122384 single base substitution A G intron_variant RECA-EU 9 34123150 34123150 single base substitution G T intron_variant RECA-EU 9 34128402 34128402 single base substitution C T upstream_gene_variant RECA-EU 9 34129838 34129838 single base substitution G T upstream_gene_variant SKCA-BR 9 34083155 34083155 insertion of <=200bp - TTC downstream_gene_variant SKCA-BR 9 34086012 34086012 single base substitution A G downstream_gene_variant SKCA-BR 9 34086469 34086469 single base substitution G A 3_prime_UTR_variant SKCA-BR 9 34086469 34086469 single base substitution G A downstream_gene_variant SKCA-BR 9 34089108 34089108 insertion of <=200bp - CAA downstream_gene_variant SKCA-BR 9 34089108 34089108 insertion of <=200bp - CAA intron_variant SKCA-BR 9 34089187 34089187 single base substitution G A downstream_gene_variant SKCA-BR 9 34089187 34089187 single base substitution G A intron_variant SKCA-BR 9 34092693 34092693 single base substitution A C intron_variant SKCA-BR 9 34094248 34094248 single base substitution C T downstream_gene_variant SKCA-BR 9 34094248 34094248 single base substitution C T intron_variant SKCA-BR 9 34094248 34094248 single base substitution C T upstream_gene_variant SKCA-BR 9 34095717 34095717 single base substitution C T downstream_gene_variant SKCA-BR 9 34095717 34095717 single base substitution C T intron_variant SKCA-BR 9 34095717 34095717 single base substitution C T upstream_gene_variant SKCA-BR 9 34096995 34096995 single base substitution G A downstream_gene_variant SKCA-BR 9 34096995 34096995 single base substitution G A intron_variant SKCA-BR 9 34096995 34096995 single base substitution G A upstream_gene_variant SKCA-BR 9 34099169 34099169 single base substitution G A intron_variant SKCA-BR 9 34099498 34099498 single base substitution G A intron_variant SKCA-BR 9 34099611 34099611 single base substitution A T intron_variant SKCA-BR 9 34101941 34101941 single base substitution G A intron_variant SKCA-BR 9 34104085 34104085 single base substitution G A downstream_gene_variant SKCA-BR 9 34104085 34104085 single base substitution G A intron_variant SKCA-BR 9 34105282 34105282 single base substitution T G downstream_gene_variant SKCA-BR 9 34105282 34105282 single base substitution T G intron_variant SKCA-BR 9 34108791 34108791 insertion of <=200bp - CAAAA intron_variant SKCA-BR 9 34108798 34108798 insertion of <=200bp - AAAAAATATAT intron_variant SKCA-BR 9 34108804 34108804 single base substitution T A intron_variant SKCA-BR 9 34108806 34108806 single base substitution A T intron_variant SKCA-BR 9 34108810 34108810 single base substitution A T intron_variant SKCA-BR 9 34108997 34109002 deletion of <=200bp TATATG - intron_variant SKCA-BR 9 34108999 34109002 deletion of <=200bp TATG - intron_variant SKCA-BR 9 34109004 34109004 single base substitution T G intron_variant SKCA-BR 9 34109330 34109330 single base substitution G A intron_variant SKCA-BR 9 34110983 34110983 insertion of <=200bp - GT intron_variant SKCA-BR 9 34111750 34111750 single base substitution G A intron_variant SKCA-BR 9 34114106 34114106 insertion of <=200bp - CA intron_variant SKCA-BR 9 34114110 34114110 single base substitution A G intron_variant SKCA-BR 9 34117697 34117697 single base substitution G A intron_variant SKCA-BR 9 34117872 34117872 single base substitution A T intron_variant SKCA-BR 9 34120667 34120667 insertion of <=200bp - CA intron_variant SKCA-BR 9 34121850 34121850 single base substitution A G intron_variant SKCA-BR 9 34123130 34123130 single base substitution G A intron_variant SKCA-BR 9 34124312 34124312 single base substitution G C intron_variant SKCA-BR 9 34126550 34126550 single base substitution T A 5_prime_UTR_variant SKCA-BR 9 34126550 34126550 single base substitution T A intron_variant SKCA-BR 9 34126550 34126550 single base substitution T A upstream_gene_variant SKCA-BR 9 34126703 34126703 single base substitution A C 5_prime_UTR_variant SKCA-BR 9 34126703 34126703 single base substitution A C intron_variant SKCA-BR 9 34126703 34126703 single base substitution A C upstream_gene_variant SKCA-BR 9 34126939 34126939 single base substitution C T intron_variant SKCA-BR 9 34126939 34126939 single base substitution C T upstream_gene_variant SKCA-BR 9 34127100 34127100 single base substitution T G intron_variant SKCA-BR 9 34127100 34127100 single base substitution T G upstream_gene_variant SKCA-BR 9 34128253 34128253 single base substitution C T upstream_gene_variant SKCA-BR 9 34129619 34129619 single base substitution C T upstream_gene_variant SKCA-BR 9 34129851 34129851 insertion of <=200bp - AAAAAGAAAAG upstream_gene_variant SKCA-BR 9 34130963 34130963 single base substitution C T upstream_gene_variant SKCA-BR 9 34132234 34132234 insertion of <=200bp - CA upstream_gene_variant SKCM-US 9 34096763 34096763 single base substitution G A downstream_gene_variant SKCM-US 9 34096763 34096763 single base substitution G A missense_variant S271F 812C>T SKCM-US 9 34096763 34096763 single base substitution G A upstream_gene_variant SKCM-US 9 34107373 34107373 single base substitution G A exon_variant SKCM-US 9 34107373 34107373 single base substitution G A missense_variant P154L 461C>T SKCM-US 9 34107373 34107373 single base substitution G A missense_variant P157L 470C>T SKCM-US 9 34107373 34107373 single base substitution G A missense_variant P175L 524C>T SKCM-US 9 34125095 34125095 single base substitution C A exon_variant SKCM-US 9 34125095 34125095 single base substitution C A missense_variant G66W 196G>T SKCM-US 9 34125095 34125095 single base substitution C A missense_variant G69W 205G>T SKCM-US 9 34125095 34125095 single base substitution C A missense_variant G87W 259G>T STAD-US 9 34089583 34089583 single base substitution G A exon_variant STAD-US 9 34089583 34089583 single base substitution G A missense_variant R344W 1030C>T STAD-US 9 34098434 34098434 single base substitution C T downstream_gene_variant STAD-US 9 34098434 34098434 single base substitution C T missense_variant R210Q 629G>A STAD-US 9 34098434 34098434 single base substitution C T missense_variant R228Q 683G>A STAD-US 9 34098434 34098434 single base substitution C T upstream_gene_variant STAD-US 9 34098435 34098435 single base substitution G A downstream_gene_variant STAD-US 9 34098435 34098435 single base substitution G A missense_variant R210W 628C>T STAD-US 9 34098435 34098435 single base substitution G A missense_variant R228W 682C>T STAD-US 9 34098435 34098435 single base substitution G A upstream_gene_variant STAD-US 9 34107458 34107458 single base substitution C T exon_variant STAD-US 9 34107458 34107458 single base substitution C T missense_variant E126K 376G>A STAD-US 9 34107458 34107458 single base substitution C T missense_variant E129K 385G>A STAD-US 9 34107458 34107458 single base substitution C T missense_variant E147K 439G>A STAD-US 9 34125105 34125106 deletion of <=200bp CT - exon_variant STAD-US 9 34125105 34125106 deletion of <=200bp CT - frameshift_variant E62 STAD-US 9 34125105 34125106 deletion of <=200bp CT - frameshift_variant E65 STAD-US 9 34125105 34125106 deletion of <=200bp CT - frameshift_variant E83 STAD-US 9 34125189 34125189 single base substitution G T exon_variant STAD-US 9 34125189 34125189 single base substitution G T synonymous_variant V34V 102C>A STAD-US 9 34125189 34125189 single base substitution G T synonymous_variant V37V 111C>A STAD-US 9 34125189 34125189 single base substitution G T synonymous_variant V55V 165C>A THCA-SA 9 34107505 34107505 single base substitution C T exon_variant THCA-SA 9 34107505 34107505 single base substitution C T missense_variant R110Q 329G>A THCA-SA 9 34107505 34107505 single base substitution C T missense_variant R113Q 338G>A THCA-SA 9 34107505 34107505 single base substitution C T missense_variant R131Q 392G>A THCA-US 9 34107509 34107509 single base substitution C A exon_variant THCA-US 9 34107509 34107509 single base substitution C A missense_variant D109Y 325G>T THCA-US 9 34107509 34107509 single base substitution C A missense_variant D112Y 334G>T THCA-US 9 34107509 34107509 single base substitution C A missense_variant D130Y 388G>T UCEC-US 9 34088427 34088427 single base substitution G A downstream_gene_variant UCEC-US 9 34088427 34088427 single base substitution G A missense_variant S428L 1283C>T UCEC-US 9 34093293 34093293 single base substitution G A exon_variant UCEC-US 9 34093293 34093293 single base substitution G A stop_gained R339* 1015C>T UCEC-US 9 34093317 34093317 single base substitution C T exon_variant UCEC-US 9 34093317 34093317 single base substitution C T missense_variant V331I 991G>A UCEC-US 9 34107400 34107400 single base substitution G A exon_variant UCEC-US 9 34107400 34107400 single base substitution G A missense_variant A145V 434C>T UCEC-US 9 34107400 34107400 single base substitution G A missense_variant A148V 443C>T UCEC-US 9 34107400 34107400 single base substitution G A missense_variant A166V 497C>T UCEC-US 9 34125241 34125241 single base substitution C A exon_variant UCEC-US 9 34125241 34125241 single base substitution C A missense_variant R17I 50G>T UCEC-US 9 34125241 34125241 single base substitution C A missense_variant R20I 59G>T UCEC-US 9 34125241 34125241 single base substitution C A missense_variant R38I 113G>T UCEC-US 9 34126353 34126353 single base substitution T C intron_variant UCEC-US 9 34126353 34126353 single base substitution T C missense_variant Q26R 77A>G UCEC-US 9 34126353 34126353 single base substitution T C upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AO-A12D-01 COSM455861 c.122C>T p.P41L Substitution - Missense 9:34125234-34125234 - TCGA-CA-6717-01 COSM1462108 c.795+1G>A p.? Unknown 9:34098323-34098323 - CSCC-7-T COSM4513978 c.957C>T p.V319V Substitution - coding silent 9:34093353-34093353 - TCGA-AM-5821-01 COSM1462110 c.393G>A p.R131R Substitution - coding silent 9:34107506-34107506 - TCGA-CF-A3MF-01 COSM1314783 c.499A>G p.I167V Substitution - Missense 9:34107400-34107400 - B96-Tumor COSM1756142 c.824A>G p.Y275C Substitution - Missense 9:34096753-34096753 - TCGA-AD-5900-01 COSM1462109 c.644_646delATG p.D215delD Deletion - In frame 9:34098473-34098475 - 3N21-VS-3T21 COSM4979392 c.913G>A p.G305S Substitution - Missense 9:34093397-34093397 - T2269 COSM2772993 c.571G>A p.A191T Substitution - Missense 9:34106464-34106464 - SNUH_G76_S1 COSM4416988 c.1024+10C>T p.? Unknown 9:34093276-34093276 - HX24T COSM3664311 c.110A>G p.K37R Substitution - Missense 9:34125246-34125246 - TCGA-HU-8602-01 COSM3906974 c.682C>T p.R228W Substitution - Missense 9:34098437-34098437 - TCGA-A6-6653-01 COSM1462107 c.1284G>A p.S428S Substitution - coding silent 9:34088428-34088428 - TCGA-AD-6899-01 COSM1462111 c.131G>A p.R44K Substitution - Missense 9:34125225-34125225 - TCGA-EL-A3T6-01 COSM3375231 c.388G>T p.D130Y Substitution - Missense 9:34107511-34107511 - T38 COSM5345781 c.271A>G p.K91E Substitution - Missense 9:34125085-34125085 - B18-Tumor COSM1756141 c.844G>A p.E282K Substitution - Missense 9:34096733-34096733 - SS6003137 COSM3665380 c.890G>A p.R297H Substitution - Missense 9:34093420-34093420 - TCGA-22-4593-01 COSM753591 c.715G>T p.A239S Substitution - Missense 9:34098404-34098404 - tumor_4108101 COSM3358334 c.1270C>G p.H424D Substitution - Missense 9:34088442-34088442 - BN50T COSM1624919 c.1215A>T p.E405D Substitution - Missense 9:34088497-34088497 - 8016470 COSM3395796 c.546A>G p.G182G Substitution - coding silent 9:34106489-34106489 - CN-AML-NR-37-Dx COSM5427962 c.937G>T p.V313L Substitution - Missense 9:34093373-34093373 - 587278 COSM1203039 c.925T>A p.S309T Substitution - Missense 9:34093385-34093385 - Pat_41_B COSM5876148 c.889C>T p.R297C Substitution - Missense 9:34093421-34093421 - TCGA-ER-A19P-06 COSM3656993 c.259G>T p.G87W Substitution - Missense 9:34125097-34125097 - B111 COSM1756143 c.369C>G p.T123T Substitution - coding silent 9:34107530-34107530 - TCGA-B0-5399-01 COSM487395 c.1262T>C p.V421A Substitution - Missense 9:34088450-34088450 - CSCC-49-T COSM4458862 c.1101C>T p.I367I Substitution - coding silent 9:34089514-34089514 - TCGA-FR-A3YN-06 COSM3656990 c.812C>T p.S271F Substitution - Missense 9:34096765-34096765 - Gp5D COSM2772997 c.407T>C p.V136A Substitution - Missense 9:34107492-34107492 - B85-0 COSM1756144 c.150G>A p.L50L Substitution - coding silent 9:34125206-34125206 - CHC433T COSM3670024 c.67C>A p.Q23K Substitution - Missense 9:34126365-34126365 - B18 COSM1756141 c.844G>A p.E282K Substitution - Missense 9:34096733-34096733 - ccRCC-30 COSM1665430 c.47_49delCGG p.P16_G17>R Complex - deletion inframe 9:34126383-34126385 - TCGA-BS-A0UM-01 COSM1108408 c.534A>G p.V178V Substitution - coding silent 9:34107365-34107365 - TCGA-BR-4255-01 COSM3906971 c.1030C>T p.R344W Substitution - Missense 9:34089585-34089585 - TCGA-G2-A2EO-01 COSM1314782 c.538G>A p.D180N Substitution - Missense 9:34107361-34107361 - SJOS001118_D1 COSM5024009 c.121C>G p.P41A Substitution - Missense 9:34125235-34125235 - CHC892T COSM4796065 c.414G>A p.Q138Q Substitution - coding silent 9:34107485-34107485 - CHC892T COSM4796065 c.414G>A p.Q138Q Substitution - coding silent 9:34107485-34107485 - HCC62T COSM1624918 c.1343_1344delAT p.Y448fs*>6 Deletion - Frameshift 9:34088368-34088369 - Gp2D COSM2772997 c.407T>C p.V136A Substitution - Missense 9:34107492-34107492 - TCGA-G2-A2EL-01 COSM1314781 c.1353C>A p.L451L Substitution - coding silent 9:34088359-34088359 - 188 COSM1741669 c.926C>G p.S309* Substitution - Nonsense 9:34093384-34093384 - ESCC_162 COSM5647956 c.178G>C p.E60Q Substitution - Missense 9:34125178-34125178 - 587376 COSM1203041 c.540+2T>C p.? Unknown 9:34107357-34107357 - WA33 COSM239521 c.457A>G p.T153A Substitution - Missense 9:34107442-34107442 - TCGA-BS-A0UV-01 COSM1108404 c.1283C>T p.S428L Substitution - Missense 9:34088429-34088429 - TCGA-B5-A11H-01 COSM1108406 c.991G>A p.V331I Substitution - Missense 9:34093319-34093319 - 587386 COSM1203040 c.1349G>A p.G450E Substitution - Missense 9:34088363-34088363 - B85-0-Tumor COSM1756144 c.150G>A p.L50L Substitution - coding silent 9:34125206-34125206 - B111-Tumor COSM1756143 c.369C>G p.T123T Substitution - coding silent 9:34107530-34107530 - 313 COSM1742089 c.709C>G p.H237D Substitution - Missense 9:34098410-34098410 - ZZUFHECRKL-G068T COSM3982834 c.1024+10C>G p.? Unknown 9:34093276-34093276 - C106 COSM4616383 c.730C>T p.P244S Substitution - Missense 9:34098389-34098389 - TCGA-D1-A103-01 COSM1108410 c.77A>G p.Q26R Substitution - Missense 9:34126355-34126355 - TCGA-CA-6718-01 COSM1462110 c.393G>A p.R131R Substitution - coding silent 9:34107506-34107506 - TCGA-EE-A29E-06 COSM3656991 c.524C>T p.P175L Substitution - Missense 9:34107375-34107375 - TCGA-AP-A051-01 COSM1108405 c.1015C>T p.R339* Substitution - Nonsense 9:34093295-34093295 - ESCC_11 COSM5624735 c.1314T>G p.G438G Substitution - coding silent 9:34088398-34088398 - SCMC_RM2_ COSM4989055 c.781A>G p.N261D Substitution - Missense 9:34098338-34098338 - CN-AML-37-T COSM5427962 c.937G>T p.V313L Substitution - Missense 9:34093373-34093373 - UM-SCC-2 COSM2772977 c.1239C>A p.D413E Substitution - Missense 9:34088473-34088473 - PT49 COSM5935471 c.864C>T p.L288L Substitution - coding silent 9:34093446-34093446 - SNUH_G45_S1 COSM3982834 c.1024+10C>G p.? Unknown 9:34093276-34093276 - TCGA-BR-8680-01 COSM3906976 c.439G>A p.E147K Substitution - Missense 9:34107460-34107460 - TCGA-AX-A0J1-01 COSM1108409 c.497C>T p.A166V Substitution - Missense 9:34107402-34107402 - B96 COSM1756142 c.824A>G p.Y275C Substitution - Missense 9:34096753-34096753 - TCGA-G2-A2ES-01 COSM1314785 c.146A>T p.Y49F Substitution - Missense 9:34125210-34125210 - TCGA-BR-8487-01 COSM3906972 c.683G>A p.R228Q Substitution - Missense 9:34098436-34098436 - LUAD-74TBW COSM355326 c.88G>A p.D30N Substitution - Missense 9:34125268-34125268 - TCGA-DK-A1AC-01 COSM1314784 c.157C>T p.R53W Substitution - Missense 9:34125199-34125199 - SNU-C1 COSM2772989 c.700C>T p.H234Y Substitution - Missense 9:34098419-34098419 - PD6413a COSM5772120 c.1032G>A p.R344R Substitution - coding silent 9:34089583-34089583 - B85-2 COSM1756145 c.141A>G p.V47V Substitution - coding silent 9:34125215-34125215 - CHC433T COSM3670024 c.67C>A p.Q23K Substitution - Missense 9:34126365-34126365 - BN50 COSM1624919 c.1215A>T p.E405D Substitution - Missense 9:34088497-34088497 - TCGA-BS-A0UF-01 COSM168266 c.113G>T p.R38I Substitution - Missense 9:34125243-34125243 - TCGA-AN-A046-01 COSM3848379 c.883T>C p.Y295H Substitution - Missense 9:34093427-34093427 - CSCC-31-T COSM4564637 c.1320_1321CC>TT p.P441S Substitution - Missense 9:34088391-34088392 - RMS208 COSM5880853 c.368C>T p.T123I Substitution - Missense 9:34107531-34107531 - TCGA-D1-A17T-01 COSM1108407 c.666G>A p.A222A Substitution - coding silent 9:34098453-34098453 - 587222 COSM1203038 c.89A>C p.D30A Substitution - Missense 9:34125267-34125267 - tumor_4135350 COSM1161781 c.933T>C p.Y311Y Substitution - coding silent 9:34093377-34093377 - CSCC-27-T COSM4457762 c.1059C>T p.I353I Substitution - coding silent 9:34089556-34089556 - T3225 COSM4676314 c.535G>T p.G179* Substitution - Nonsense 9:34107364-34107364 - BK0084 COSM4188722 c.1208A>C p.H403P Substitution - Missense 9:34088504-34088504 - ASHPC_0003_Pa_P_2 COSM3782237 c.829C>T p.H277Y Substitution - Missense 9:34096748-34096748 - B85-2-Tumor COSM1756145 c.141A>G p.V47V Substitution - coding silent 9:34125215-34125215 - S02194 COSM5674967 c.152A>G p.K51R Substitution - Missense 9:34125204-34125204 - TCGA-A2-A3Y0-01 COSM3848380 c.147C>T p.Y49Y Substitution - coding silent 9:34125209-34125209 - TCGA-BR-8369-01 COSM3906978 c.165C>A p.V55V Substitution - coding silent 9:34125191-34125191 - SWE-2A COSM1178212 c.1180C>A p.L394I Substitution - Missense 9:34089435-34089435 - TCGA-RG-A7D4-01 COSM4918696 c.1085T>C p.L362P Substitution - Missense 9:34089530-34089530 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.493750 9p13.3 2418072|CGAP|BC063823|A/G|non-coding||2614|Validated; 1529196|dbSNP|BC008893|A/G|non-coding||2268|Validated; 1529196|dbSNP|BC063823|A/G|non-coding||2614|Validated Hs.741268;Hs.741270 9p13.3 600207 2418072|CGAP|BC063823|A/G|non-coding||2614|Validated; 1529196|dbSNP|BC008893|A/G|non-coding||2268|Validated; 1529196|dbSNP|BC063823|A/G|non-coding||2614|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Synonymous p.Y311Y c.933T>C 9 34093375 DLBCL A T IntronicSNV . c.861+105T>A 9 34096609 HC C A IntronicSNV . c.796-36G>T 9 34096815 CLL C A Missense p.A239S c.715G>T 9 34098402 LUSC C A Missense p.D130Y c.388G>T 9 34107509 THCA C A Missense p.G87W c.259G>T 9 34125095 CM C A Missense p.V104L c.310G>T 9 34125044 LUAD C G Missense p.R53P c.158G>C 9 34125196 HNSC C G Missense p.V334L c.1000G>C 9 34093308 BRCA C T Missense p.D180N c.538G>A 9 34107359 BLCA C T Missense p.V331I c.991G>A 9 34093317 UCEC G A IntronicSNV . c.334-1782C>T 9 34109345 CM G A IntronicSNV . c.334-2179C>T 9 34109742 CM G A Missense p.P41L c.122C>T 9 34125232 BRCA G A Missense p.R344W c.1030C>T 9 34089583 STAD G A Missense p.S15L c.44C>T 9 34126386 LUAD G C Missense p.H424D c.1270C>G 9 34088440 DLBCL G C Missense p.I235M c.705C>G 9 34098412 HNSC G C Synonymous p.G140G c.420C>G 9 34107477 HNSC G T Synonymous p.L451L c.1353C>A 9 34088357 BLCA G T Synonymous p.T291T c.873C>A 9 34093435 LUAD T A Missense p.Y49F c.146A>T 9 34125208 BLCA T C IntronicSNV . c.1025-434A>G 9 34090022 HC T C IntronicSNV . c.333+5948A>G 9 34119073 CLL T C Missense p.I167V c.499A>G 9 34107398 BLCA