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 137019624 137019624 + Missense_Mutation SNP C C A TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr9:137019624C>A c.668C>A c.(667-669)tCc>tAc p.S223Y BRCA 9 137005008 137005010 + In_Frame_Del DEL GGA GGA - TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr9:137005008_137005010delGGA c.9_11delGGA c.(7-12)acggag>acg p.E5del BRCA 9 137013427 137013427 + Silent SNP T T C TCGA-OL-A66I-01A-21D-A29N-09 TCGA-OL-A66I-10A-01D-A29N-09 g.chr9:137013427T>C c.546T>C c.(544-546)gaT>gaC p.D182D BRCA 9 137021657 137021657 + Silent SNP T T A TCGA-A8-A06Z-01A-11W-A019-09 TCGA-A8-A06Z-10A-01W-A021-09 g.chr9:137021657T>A c.846T>A c.(844-846)ctT>ctA p.L282L COAD 9 137005842 137005842 + Silent SNP A A G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:137005842A>G c.99A>G c.(97-99)ccA>ccG p.P33P COAD 9 137007763 137007763 + Silent SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr9:137007763C>T c.450C>T c.(448-450)gaC>gaT p.D150D COAD 9 137013408 137013408 + Splice_Site SNP A A G TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr9:137013408A>G c.e8-1 COAD 9 137013455 137013455 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:137013455G>A c.574G>A c.(574-576)Gat>Aat p.D192N COAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COAD 9 137021685 137021685 + Missense_Mutation SNP G G C TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr9:137021685G>C c.874G>C c.(874-876)Gag>Cag p.E292Q COADREAD 9 137005842 137005842 + Silent SNP A A G TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr9:137005842A>G c.99A>G c.(97-99)ccA>ccG p.P33P COADREAD 9 137007763 137007763 + Silent SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr9:137007763C>T c.450C>T c.(448-450)gaC>gaT p.D150D COADREAD 9 137013408 137013408 + Splice_Site SNP A A G TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr9:137013408A>G c.e8-1 COADREAD 9 137013455 137013455 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:137013455G>A c.574G>A c.(574-576)Gat>Aat p.D192N COADREAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COADREAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COADREAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs COADREAD 9 137021685 137021685 + Missense_Mutation SNP G G C TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr9:137021685G>C c.874G>C c.(874-876)Gag>Cag p.E292Q ESCA 9 137013436 137013436 + Missense_Mutation SNP G G T TCGA-R6-A8W5-01B-11D-A37C-09 TCGA-R6-A8W5-10A-01D-A37F-09 g.chr9:137013436G>T c.555G>T c.(553-555)ttG>ttT p.L185F GBMLGG 9 137005847 137005847 + Missense_Mutation SNP A A G TCGA-FG-6690-01A-11D-1893-08 TCGA-FG-6690-10A-01D-1893-08 g.chr9:137005847A>G c.104A>G c.(103-105)tAt>tGt p.Y35C HNSC 9 137005026 137005026 + Missense_Mutation SNP G G C TCGA-DQ-7591-01A-11D-2078-08 TCGA-DQ-7591-10A-01D-2078-08 g.chr9:137005026G>C c.27G>C c.(25-27)gaG>gaC p.E9D HNSC 9 137017113 137017113 + Nonsense_Mutation SNP G G A TCGA-CR-7367-01A-11D-2012-08 TCGA-CR-7367-10A-01D-2013-08 g.chr9:137017113G>A c.593G>A c.(592-594)tGg>tAg p.W198* KIPAN 9 137006663 137006663 + Silent SNP G G A TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr9:137006663G>A c.222G>A c.(220-222)gcG>gcA p.A74A KIPAN 9 137007499 137007499 + Missense_Mutation SNP T T G TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chr9:137007499T>G c.399T>G c.(397-399)ttT>ttG p.F133L KIRC 9 137006663 137006663 + Silent SNP G G A TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr9:137006663G>A c.222G>A c.(220-222)gcG>gcA p.A74A KIRC 9 137007499 137007499 + Missense_Mutation SNP T T G TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chr9:137007499T>G c.399T>G c.(397-399)ttT>ttG p.F133L LGG 9 137005847 137005847 + Missense_Mutation SNP A A G TCGA-FG-6690-01A-11D-1893-08 TCGA-FG-6690-10A-01D-1893-08 g.chr9:137005847A>G c.104A>G c.(103-105)tAt>tGt p.Y35C LIHC 9 137023031 137023031 + Silent SNP A A T TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chr9:137023031A>T c.921A>T c.(919-921)acA>acT p.T307T LIHC 9 137023062 137023062 + Missense_Mutation SNP T T C TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr9:137023062T>C c.952T>C c.(952-954)Tct>Cct p.S318P LUAD 9 137005059 137005059 + Silent SNP G G T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr9:137005059G>T c.60G>T c.(58-60)tcG>tcT p.S20S LUAD 9 137007123 137007123 + Nonsense_Mutation SNP C C G TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr9:137007123C>G c.317C>G c.(316-318)tCa>tGa p.S106* LUAD 9 137007537 137007537 + Nonsense_Mutation SNP C C G TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr9:137007537C>G c.437C>G c.(436-438)tCa>tGa p.S146* LUAD 9 137017125 137017125 + Missense_Mutation SNP C C T TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr9:137017125C>T c.605C>T c.(604-606)tCa>tTa p.S202L PAAD 9 137017152 137017152 + Splice_Site SNP G G A TCGA-3A-A9IS-01A-21D-A397-08 TCGA-3A-A9IS-10A-01D-A39A-08 g.chr9:137017152G>A c.e9+1 PAAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs PAAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-RB-AA9M-01A-11D-A397-08 TCGA-RB-AA9M-10A-01D-A39A-08 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs PAAD 9 137019598 137019598 + Frame_Shift_Del DEL C C - TCGA-RL-AAAS-01A-32D-A397-08 TCGA-RL-AAAS-10A-01D-A39A-08 g.chr9:137019598delC c.642delC c.(640-642)aacfs p.N214fs PAAD 9 137019649 137019649 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:137019649C>T c.693C>T c.(691-693)gcC>gcT p.A231A PRAD 9 137023095 137023095 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:137023095C>T c.985C>T c.(985-987)Ctg>Ttg p.L329L SKCM 9 137007496 137007496 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:137007496C>T c.396C>T c.(394-396)gtC>gtT p.V132V SKCM 9 137007825 137007825 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr9:137007825C>T c.512C>T c.(511-513)tCg>tTg p.S171L SKCM 9 137013422 137013422 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr9:137013422C>T c.541C>T c.(541-543)Cgt>Tgt p.R181C

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BRCA-EU 9 136996267 136996267 single base substitution G C upstream_gene_variant BRCA-EU 9 136997232 136997232 single base substitution C T upstream_gene_variant BRCA-EU 9 136999070 136999070 single base substitution C G upstream_gene_variant BRCA-EU 9 137000467 137000467 single base substitution C A upstream_gene_variant BRCA-EU 9 137001597 137001597 single base substitution G C intron_variant BRCA-EU 9 137001597 137001597 single base substitution G C upstream_gene_variant BRCA-EU 9 137002365 137002365 single base substitution G T intron_variant BRCA-EU 9 137002365 137002365 single base substitution G T upstream_gene_variant BRCA-EU 9 137004313 137004313 single base substitution C T intron_variant BRCA-EU 9 137004313 137004313 single base substitution C T upstream_gene_variant BRCA-EU 9 137005752 137005752 single base substitution A C intron_variant BRCA-EU 9 137006089 137006118 deletion of <=200bp TGTGAGCTCAGTGCTGGTTGAAATTGCCCG - downstream_gene_variant BRCA-EU 9 137006089 137006118 deletion of <=200bp TGTGAGCTCAGTGCTGGTTGAAATTGCCCG - intron_variant BRCA-EU 9 137010113 137010122 deletion of <=200bp CTTTAAATAA - downstream_gene_variant BRCA-EU 9 137010113 137010122 deletion of <=200bp CTTTAAATAA - intron_variant BRCA-EU 9 137011978 137011978 single base substitution G A downstream_gene_variant BRCA-EU 9 137011978 137011978 single base substitution G A intron_variant BRCA-EU 9 137014284 137014284 deletion of <=200bp G - intron_variant BRCA-EU 9 137014323 137014323 single base substitution C T intron_variant BRCA-EU 9 137015014 137015014 single base substitution G C intron_variant BRCA-EU 9 137015536 137015536 single base substitution G A intron_variant BRCA-EU 9 137017447 137017447 single base substitution A G intron_variant BRCA-EU 9 137020250 137020255 deletion of <=200bp ATACTT - intron_variant BRCA-EU 9 137020384 137020384 single base substitution G A intron_variant BRCA-EU 9 137020456 137020456 single base substitution T C splice_region_variant BRCA-EU 9 137021495 137021495 single base substitution G A intron_variant BRCA-EU 9 137021759 137021759 single base substitution G A intron_variant BRCA-EU 9 137021906 137021906 single base substitution C G intron_variant BRCA-EU 9 137022018 137022018 single base substitution C T intron_variant BRCA-EU 9 137023007 137023007 single base substitution G A intron_variant BRCA-EU 9 137023042 137023042 single base substitution C A missense_variant P311Q 932C>A BRCA-EU 9 137023485 137023485 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 137024295 137024295 single base substitution G T 3_prime_UTR_variant BRCA-EU 9 137024522 137024522 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 137026176 137026176 single base substitution G A downstream_gene_variant BRCA-EU 9 137026178 137026178 single base substitution A G downstream_gene_variant BRCA-EU 9 137026928 137026928 single base substitution G C downstream_gene_variant BRCA-EU 9 137027201 137027201 single base substitution C G downstream_gene_variant BRCA-EU 9 137028264 137028264 single base substitution C G downstream_gene_variant BRCA-EU 9 137028521 137028521 single base substitution C T downstream_gene_variant BRCA-EU 9 137029222 137029222 single base substitution A G downstream_gene_variant BRCA-EU 9 137029691 137029691 single base substitution C A downstream_gene_variant BRCA-EU 9 137029834 137029834 single base substitution C T downstream_gene_variant BRCA-EU 9 137029837 137029837 single base substitution C T downstream_gene_variant BRCA-EU 9 137029983 137029983 single base substitution A T downstream_gene_variant BRCA-FR 9 137001597 137001597 single base substitution G C intron_variant BRCA-FR 9 137001597 137001597 single base substitution G C upstream_gene_variant BRCA-FR 9 137002365 137002365 single base substitution G T intron_variant BRCA-FR 9 137002365 137002365 single base substitution G T upstream_gene_variant BRCA-FR 9 137021759 137021759 single base substitution G A intron_variant BRCA-FR 9 137021906 137021906 single base substitution C G intron_variant BRCA-FR 9 137022018 137022018 single base substitution C T intron_variant BRCA-FR 9 137023485 137023485 single base substitution G A 3_prime_UTR_variant BRCA-FR 9 137026176 137026176 single base substitution G A downstream_gene_variant BRCA-FR 9 137028264 137028264 single base substitution C G downstream_gene_variant BRCA-FR 9 137028521 137028521 single base substitution C T downstream_gene_variant BRCA-UK 9 136999704 136999704 single base substitution G A upstream_gene_variant BRCA-UK 9 137028764 137028764 single base substitution C T downstream_gene_variant BRCA-US 9 137005008 137005010 deletion of <=200bp GGA - inframe_deletion TE3T BRCA-US 9 137013427 137013427 single base substitution T C synonymous_variant D182D 546T>C BRCA-US 9 137019597 137019597 insertion of <=200bp - C frameshift_variant N214T? BRCA-US 9 137021657 137021657 single base substitution T A synonymous_variant L282L 846T>A BTCA-JP 9 137005053 137005053 single base substitution C T synonymous_variant T18T 54C>T BTCA-JP 9 137007730 137007730 single base substitution A G downstream_gene_variant BTCA-JP 9 137007730 137007730 single base substitution A G intron_variant BTCA-JP 9 137017120 137017120 single base substitution C T synonymous_variant T200T 600C>T BTCA-JP 9 137017290 137017290 single base substitution G A intron_variant BTCA-JP 9 137021833 137021833 single base substitution C T intron_variant CLLE-ES 9 137029560 137029560 single base substitution A T downstream_gene_variant COAD-US 9 137007763 137007763 single base substitution C T downstream_gene_variant COAD-US 9 137007763 137007763 single base substitution C T synonymous_variant D150D 450C>T COAD-US 9 137013408 137013408 single base substitution A G splice_acceptor_variant COAD-US 9 137019598 137019598 deletion of <=200bp C - frameshift_variant N214 COAD-US 9 137021685 137021685 single base substitution G C missense_variant E292Q 874G>C COCA-CN 9 137005008 137005008 single base substitution G A synonymous_variant T3T 9G>A COCA-CN 9 137005961 137005961 single base substitution T C downstream_gene_variant COCA-CN 9 137005961 137005961 single base substitution T C intron_variant COCA-CN 9 137006687 137006687 single base substitution C T downstream_gene_variant COCA-CN 9 137006687 137006687 single base substitution C T synonymous_variant T82T 246C>T COCA-CN 9 137007298 137007298 single base substitution G A downstream_gene_variant COCA-CN 9 137007298 137007298 single base substitution G A intron_variant COCA-CN 9 137010225 137010225 single base substitution T G downstream_gene_variant COCA-CN 9 137010225 137010225 single base substitution T G intron_variant COCA-CN 9 137020750 137020750 single base substitution C T intron_variant COCA-CN 9 137021803 137021803 single base substitution C T intron_variant COCA-CN 9 137028160 137028160 single base substitution C T downstream_gene_variant EOPC-DE 9 137011020 137011020 single base substitution G C downstream_gene_variant EOPC-DE 9 137011020 137011020 single base substitution G C intron_variant ESAD-UK 9 136995996 136995996 single base substitution A C upstream_gene_variant ESAD-UK 9 136998298 136998298 single base substitution A G upstream_gene_variant ESAD-UK 9 136998826 136998826 single base substitution G A upstream_gene_variant ESAD-UK 9 137006206 137006206 single base substitution G A downstream_gene_variant ESAD-UK 9 137006206 137006206 single base substitution G A intron_variant ESAD-UK 9 137008181 137008181 single base substitution C T downstream_gene_variant ESAD-UK 9 137008181 137008181 single base substitution C T intron_variant ESAD-UK 9 137008762 137008762 single base substitution C T downstream_gene_variant ESAD-UK 9 137008762 137008762 single base substitution C T intron_variant ESAD-UK 9 137009975 137009975 single base substitution G A downstream_gene_variant ESAD-UK 9 137009975 137009975 single base substitution G A intron_variant ESAD-UK 9 137011758 137011758 single base substitution G A downstream_gene_variant ESAD-UK 9 137011758 137011758 single base substitution G A intron_variant ESAD-UK 9 137012009 137012009 single base substitution C A downstream_gene_variant ESAD-UK 9 137012009 137012009 single base substitution C A intron_variant ESAD-UK 9 137013047 137013047 single base substitution C T intron_variant ESAD-UK 9 137018692 137018692 single base substitution A G intron_variant ESAD-UK 9 137020320 137020320 single base substitution C T intron_variant ESAD-UK 9 137021237 137021237 single base substitution A T intron_variant ESAD-UK 9 137022400 137022400 single base substitution C T intron_variant ESAD-UK 9 137023211 137023211 deletion of <=200bp G - 3_prime_UTR_variant ESAD-UK 9 137023359 137023359 single base substitution G A 3_prime_UTR_variant ESAD-UK 9 137023434 137023434 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 9 137024909 137024909 single base substitution G A 3_prime_UTR_variant ESAD-UK 9 137028995 137028995 single base substitution G A downstream_gene_variant ESAD-UK 9 137029903 137029903 single base substitution A C downstream_gene_variant ESAD-UK 9 137029983 137029983 single base substitution A T downstream_gene_variant ESCA-CN 9 137007292 137007292 single base substitution T G downstream_gene_variant ESCA-CN 9 137007292 137007292 single base substitution T G intron_variant ESCA-CN 9 137007970 137007970 single base substitution G A downstream_gene_variant ESCA-CN 9 137007970 137007970 single base substitution G A intron_variant KIRC-US 9 137006663 137006663 single base substitution G A downstream_gene_variant KIRC-US 9 137006663 137006663 single base substitution G A synonymous_variant A74A 222G>A LAML-KR 9 137010239 137010239 single base substitution G T downstream_gene_variant LAML-KR 9 137010239 137010239 single base substitution G T intron_variant LICA-FR 9 136995812 136995812 single base substitution G A upstream_gene_variant LICA-FR 9 137005118 137005118 single base substitution C T intron_variant LICA-FR 9 137008923 137008923 single base substitution C T downstream_gene_variant LICA-FR 9 137008923 137008923 single base substitution C T intron_variant LINC-JP 9 136998889 136998889 single base substitution A G upstream_gene_variant LINC-JP 9 136998891 136998891 single base substitution A G upstream_gene_variant LINC-JP 9 136999445 136999445 single base substitution G A upstream_gene_variant LINC-JP 9 137005003 137005003 single base substitution G C missense_variant A2P 4G>C LINC-JP 9 137005115 137005115 single base substitution G A intron_variant LINC-JP 9 137005293 137005293 single base substitution A G intron_variant LINC-JP 9 137006420 137006420 single base substitution G C downstream_gene_variant LINC-JP 9 137006420 137006420 single base substitution G C intron_variant LINC-JP 9 137014109 137014109 single base substitution G A intron_variant LIRI-JP 9 136995882 136995882 single base substitution A T upstream_gene_variant LIRI-JP 9 136998959 136998959 deletion of <=200bp C - upstream_gene_variant LIRI-JP 9 137001876 137001876 single base substitution C T intron_variant LIRI-JP 9 137001876 137001876 single base substitution C T upstream_gene_variant LIRI-JP 9 137002228 137002228 single base substitution A G intron_variant LIRI-JP 9 137002228 137002228 single base substitution A G upstream_gene_variant LIRI-JP 9 137003468 137003468 insertion of <=200bp - C intron_variant LIRI-JP 9 137003468 137003468 insertion of <=200bp - C upstream_gene_variant LIRI-JP 9 137004757 137004757 single base substitution G T intron_variant LIRI-JP 9 137004757 137004757 single base substitution G T upstream_gene_variant LIRI-JP 9 137011650 137011650 single base substitution G A downstream_gene_variant LIRI-JP 9 137011650 137011650 single base substitution G A intron_variant LIRI-JP 9 137011732 137011732 single base substitution C A downstream_gene_variant LIRI-JP 9 137011732 137011732 single base substitution C A intron_variant LIRI-JP 9 137012380 137012380 single base substitution C T intron_variant LIRI-JP 9 137013689 137013689 single base substitution T C intron_variant LIRI-JP 9 137015953 137015953 single base substitution T C intron_variant LIRI-JP 9 137015976 137015976 single base substitution A G intron_variant LIRI-JP 9 137024954 137024954 single base substitution G A 3_prime_UTR_variant LIRI-JP 9 137027353 137027353 single base substitution A C downstream_gene_variant LIRI-JP 9 137027801 137027801 single base substitution A T downstream_gene_variant LIRI-JP 9 137029731 137029731 single base substitution T C downstream_gene_variant LIRI-JP 9 137029895 137029895 single base substitution T G downstream_gene_variant LUSC-KR 9 136999023 136999023 single base substitution T C upstream_gene_variant LUSC-KR 9 137007123 137007123 single base substitution C T downstream_gene_variant LUSC-KR 9 137007123 137007123 single base substitution C T missense_variant S106L 317C>T LUSC-KR 9 137010225 137010225 single base substitution T G downstream_gene_variant LUSC-KR 9 137010225 137010225 single base substitution T G intron_variant LUSC-KR 9 137013006 137013006 single base substitution G A intron_variant LUSC-KR 9 137014915 137014915 single base substitution G T intron_variant LUSC-KR 9 137015655 137015655 single base substitution C T intron_variant LUSC-KR 9 137016621 137016621 single base substitution G T intron_variant LUSC-KR 9 137019776 137019776 single base substitution G A intron_variant LUSC-KR 9 137020474 137020474 single base substitution C T synonymous_variant L240L 720C>T LUSC-KR 9 137022157 137022157 single base substitution A T intron_variant LUSC-KR 9 137024963 137024963 single base substitution G T 3_prime_UTR_variant LUSC-KR 9 137024964 137024964 single base substitution G T 3_prime_UTR_variant LUSC-KR 9 137029691 137029691 single base substitution C G downstream_gene_variant LUSC-KR 9 137029794 137029794 single base substitution C T downstream_gene_variant MALY-DE 9 136997917 136997917 single base substitution A C upstream_gene_variant MALY-DE 9 137010062 137010062 single base substitution T C downstream_gene_variant MALY-DE 9 137010062 137010062 single base substitution T C intron_variant MALY-DE 9 137027800 137027800 single base substitution C T downstream_gene_variant MELA-AU 9 136995496 136995496 single base substitution C T upstream_gene_variant MELA-AU 9 136995586 136995586 single base substitution C T upstream_gene_variant MELA-AU 9 136995634 136995634 single base substitution G A upstream_gene_variant MELA-AU 9 136996255 136996255 single base substitution C T upstream_gene_variant MELA-AU 9 136996333 136996333 single base substitution G A upstream_gene_variant MELA-AU 9 136996334 136996334 single base substitution G A upstream_gene_variant MELA-AU 9 136996343 136996343 single base substitution C T upstream_gene_variant MELA-AU 9 136996432 136996432 single base substitution G A upstream_gene_variant MELA-AU 9 136996815 136996815 single base substitution G A upstream_gene_variant MELA-AU 9 136997190 136997190 single base substitution G A upstream_gene_variant MELA-AU 9 136997208 136997208 single base substitution G A upstream_gene_variant MELA-AU 9 136997487 136997487 single base substitution G A upstream_gene_variant MELA-AU 9 136997703 136997703 single base substitution G A upstream_gene_variant MELA-AU 9 136997899 136997899 single base substitution G A upstream_gene_variant MELA-AU 9 136998185 136998185 single base substitution G A upstream_gene_variant MELA-AU 9 136999210 136999210 single base substitution T A upstream_gene_variant MELA-AU 9 136999425 136999425 single base substitution G A upstream_gene_variant MELA-AU 9 136999605 136999606 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 9 136999808 136999808 single base substitution G A upstream_gene_variant MELA-AU 9 137000064 137000064 single base substitution G A upstream_gene_variant MELA-AU 9 137000366 137000366 single base substitution G A upstream_gene_variant MELA-AU 9 137002706 137002706 single base substitution T C intron_variant MELA-AU 9 137002706 137002706 single base substitution T C upstream_gene_variant MELA-AU 9 137003099 137003099 single base substitution C T intron_variant MELA-AU 9 137003099 137003099 single base substitution C T upstream_gene_variant MELA-AU 9 137003162 137003162 single base substitution C T intron_variant MELA-AU 9 137003162 137003162 single base substitution C T upstream_gene_variant MELA-AU 9 137003240 137003240 single base substitution T C intron_variant MELA-AU 9 137003240 137003240 single base substitution T C upstream_gene_variant MELA-AU 9 137003310 137003310 single base substitution C T intron_variant MELA-AU 9 137003310 137003310 single base substitution C T upstream_gene_variant MELA-AU 9 137006891 137006891 single base substitution C T downstream_gene_variant MELA-AU 9 137006891 137006891 single base substitution C T intron_variant MELA-AU 9 137007396 137007396 single base substitution C T downstream_gene_variant MELA-AU 9 137007396 137007396 single base substitution C T intron_variant MELA-AU 9 137007650 137007650 single base substitution C T downstream_gene_variant MELA-AU 9 137007650 137007650 single base substitution C T intron_variant MELA-AU 9 137007995 137007995 single base substitution G A downstream_gene_variant MELA-AU 9 137007995 137007995 single base substitution G A intron_variant MELA-AU 9 137009689 137009689 single base substitution C T downstream_gene_variant MELA-AU 9 137009689 137009689 single base substitution C T intron_variant MELA-AU 9 137009914 137009914 single base substitution T C downstream_gene_variant MELA-AU 9 137009914 137009914 single base substitution T C intron_variant MELA-AU 9 137012040 137012040 single base substitution A G downstream_gene_variant MELA-AU 9 137012040 137012040 single base substitution A G intron_variant MELA-AU 9 137012919 137012919 single base substitution A T intron_variant MELA-AU 9 137013074 137013074 single base substitution C T intron_variant MELA-AU 9 137013329 137013329 single base substitution T C intron_variant MELA-AU 9 137013405 137013405 single base substitution C T splice_region_variant MELA-AU 9 137014555 137014555 single base substitution G A intron_variant MELA-AU 9 137014749 137014749 single base substitution C T intron_variant MELA-AU 9 137015314 137015314 single base substitution G A intron_variant MELA-AU 9 137015782 137015782 single base substitution C T intron_variant MELA-AU 9 137016950 137016950 single base substitution G A intron_variant MELA-AU 9 137017279 137017279 single base substitution C T intron_variant MELA-AU 9 137017283 137017283 single base substitution C T intron_variant MELA-AU 9 137017669 137017669 single base substitution C T intron_variant MELA-AU 9 137018119 137018119 single base substitution C T intron_variant MELA-AU 9 137018181 137018181 single base substitution C T intron_variant MELA-AU 9 137018267 137018268 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 137018518 137018518 single base substitution T C intron_variant MELA-AU 9 137018796 137018796 single base substitution C T intron_variant MELA-AU 9 137019284 137019284 single base substitution C T intron_variant MELA-AU 9 137019430 137019430 single base substitution C T intron_variant MELA-AU 9 137019536 137019536 single base substitution C T intron_variant MELA-AU 9 137019573 137019573 single base substitution C T intron_variant MELA-AU 9 137019574 137019574 single base substitution C T intron_variant MELA-AU 9 137019704 137019704 single base substitution C T intron_variant MELA-AU 9 137019972 137019972 single base substitution C T intron_variant MELA-AU 9 137020191 137020191 single base substitution C T intron_variant MELA-AU 9 137020952 137020952 single base substitution C T intron_variant MELA-AU 9 137021608 137021608 single base substitution C T intron_variant MELA-AU 9 137021770 137021770 single base substitution C T intron_variant MELA-AU 9 137022027 137022027 single base substitution C T intron_variant MELA-AU 9 137022033 137022033 single base substitution C T intron_variant MELA-AU 9 137022207 137022207 single base substitution C T intron_variant MELA-AU 9 137022418 137022418 single base substitution C T intron_variant MELA-AU 9 137023119 137023119 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137023127 137023127 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137023394 137023394 single base substitution T C 3_prime_UTR_variant MELA-AU 9 137023594 137023594 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137023967 137023967 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137024095 137024095 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137024495 137024496 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 9 137024503 137024503 single base substitution C T 3_prime_UTR_variant MELA-AU 9 137025823 137025823 single base substitution C T downstream_gene_variant MELA-AU 9 137026198 137026198 single base substitution C T downstream_gene_variant MELA-AU 9 137026247 137026247 single base substitution C T downstream_gene_variant MELA-AU 9 137026642 137026642 single base substitution G A downstream_gene_variant MELA-AU 9 137026807 137026807 single base substitution C T downstream_gene_variant MELA-AU 9 137026986 137026986 single base substitution G A downstream_gene_variant MELA-AU 9 137027368 137027368 single base substitution G A downstream_gene_variant MELA-AU 9 137027992 137027992 single base substitution G A downstream_gene_variant MELA-AU 9 137029584 137029584 single base substitution G A downstream_gene_variant MELA-AU 9 137029619 137029619 single base substitution G T downstream_gene_variant MELA-AU 9 137029639 137029639 single base substitution C T downstream_gene_variant MELA-AU 9 137029640 137029640 single base substitution C T downstream_gene_variant MELA-AU 9 137029652 137029652 single base substitution G A downstream_gene_variant MELA-AU 9 137029720 137029720 single base substitution G A downstream_gene_variant MELA-AU 9 137029767 137029767 single base substitution C T downstream_gene_variant MELA-AU 9 137029768 137029768 single base substitution A G downstream_gene_variant MELA-AU 9 137029795 137029795 single base substitution G A downstream_gene_variant MELA-AU 9 137029861 137029861 single base substitution G A downstream_gene_variant MELA-AU 9 137029867 137029867 single base substitution A G downstream_gene_variant MELA-AU 9 137029886 137029886 single base substitution C T downstream_gene_variant MELA-AU 9 137029972 137029972 single base substitution G A downstream_gene_variant MELA-AU 9 137029973 137029973 single base substitution G A downstream_gene_variant MELA-AU 9 137030031 137030031 single base substitution G A downstream_gene_variant MELA-AU 9 137030031 137030032 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 137030032 137030032 single base substitution G A downstream_gene_variant MELA-AU 9 137030036 137030036 single base substitution G A downstream_gene_variant MELA-AU 9 137030050 137030051 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant ORCA-IN 9 137005151 137005151 single base substitution A G intron_variant OV-AU 9 137001090 137001090 single base substitution G T intron_variant OV-AU 9 137001090 137001090 single base substitution G T upstream_gene_variant OV-AU 9 137003722 137003722 single base substitution C G intron_variant OV-AU 9 137003722 137003722 single base substitution C G upstream_gene_variant OV-AU 9 137018670 137018670 single base substitution G A intron_variant OV-AU 9 137022074 137022074 single base substitution A C intron_variant OV-AU 9 137028190 137028190 single base substitution G A downstream_gene_variant OV-AU 9 137029080 137029080 single base substitution G C downstream_gene_variant OV-AU 9 137029738 137029738 single base substitution T C downstream_gene_variant OV-AU 9 137029741 137029741 single base substitution G A downstream_gene_variant OV-AU 9 137029856 137029856 single base substitution T G downstream_gene_variant PACA-AU 9 137001240 137001240 single base substitution T A 5_prime_UTR_variant PACA-AU 9 137001240 137001240 single base substitution T A intron_variant PACA-AU 9 137001240 137001240 single base substitution T A upstream_gene_variant PACA-AU 9 137005619 137005619 single base substitution T G intron_variant PACA-AU 9 137008794 137008794 single base substitution C T downstream_gene_variant PACA-AU 9 137008794 137008794 single base substitution C T intron_variant PACA-AU 9 137008948 137008948 deletion of <=200bp T - downstream_gene_variant PACA-AU 9 137008948 137008948 deletion of <=200bp T - intron_variant PACA-AU 9 137010961 137010961 single base substitution C T downstream_gene_variant PACA-AU 9 137010961 137010961 single base substitution C T intron_variant PACA-AU 9 137014675 137014675 single base substitution A C intron_variant PACA-AU 9 137027297 137027297 single base substitution G T downstream_gene_variant PACA-AU 9 137028998 137028998 single base substitution C A downstream_gene_variant PACA-CA 9 136999013 136999013 single base substitution G A upstream_gene_variant PACA-CA 9 137000187 137000187 single base substitution T C upstream_gene_variant PACA-CA 9 137006681 137006681 single base substitution G A downstream_gene_variant PACA-CA 9 137006681 137006681 single base substitution G A synonymous_variant E80E 240G>A PACA-CA 9 137017213 137017213 single base substitution G T intron_variant PACA-CA 9 137017609 137017609 single base substitution C T intron_variant PACA-CA 9 137019598 137019598 deletion of <=200bp C - frameshift_variant N214 PACA-CA 9 137025481 137025481 single base substitution C T downstream_gene_variant PACA-CA 9 137027629 137027629 single base substitution G T downstream_gene_variant PACA-CA 9 137029773 137029773 single base substitution G A downstream_gene_variant PBCA-DE 9 136997745 136997745 single base substitution G A upstream_gene_variant PBCA-DE 9 137027343 137027343 single base substitution C T downstream_gene_variant PBCA-DE 9 137028578 137028578 single base substitution G A downstream_gene_variant PRAD-CA 9 136996807 136996807 single base substitution C T upstream_gene_variant PRAD-CA 9 137003562 137003562 single base substitution G A intron_variant PRAD-CA 9 137003562 137003562 single base substitution G A upstream_gene_variant PRAD-CA 9 137005235 137005235 single base substitution G A intron_variant PRAD-CA 9 137028107 137028107 single base substitution A C downstream_gene_variant PRAD-UK 9 137014647 137014647 single base substitution G A intron_variant PRAD-UK 9 137016130 137016130 single base substitution C T intron_variant PRAD-UK 9 137017609 137017609 single base substitution C T intron_variant PRAD-UK 9 137018876 137018876 insertion of <=200bp - GG intron_variant PRAD-UK 9 137028540 137028540 single base substitution G A downstream_gene_variant PRAD-UK 9 137028547 137028547 single base substitution C T downstream_gene_variant PRAD-UK 9 137028834 137028834 single base substitution G A downstream_gene_variant RECA-EU 9 136996545 136996545 single base substitution A G upstream_gene_variant RECA-EU 9 137004026 137004026 single base substitution G T intron_variant RECA-EU 9 137004026 137004026 single base substitution G T upstream_gene_variant RECA-EU 9 137007828 137007828 single base substitution A C downstream_gene_variant RECA-EU 9 137007828 137007828 single base substitution A C missense_variant D172A 515A>C RECA-EU 9 137021091 137021091 single base substitution G C intron_variant SKCA-BR 9 136999095 136999095 single base substitution T G upstream_gene_variant SKCA-BR 9 136999144 136999144 single base substitution G A upstream_gene_variant SKCA-BR 9 137000023 137000023 single base substitution G A upstream_gene_variant SKCA-BR 9 137001294 137001294 single base substitution C T 5_prime_UTR_variant SKCA-BR 9 137001294 137001294 single base substitution C T intron_variant SKCA-BR 9 137001294 137001294 single base substitution C T upstream_gene_variant SKCA-BR 9 137001319 137001319 single base substitution G A 5_prime_UTR_variant SKCA-BR 9 137001319 137001319 single base substitution G A intron_variant SKCA-BR 9 137001319 137001319 single base substitution G A upstream_gene_variant SKCA-BR 9 137001555 137001555 single base substitution A C intron_variant SKCA-BR 9 137001555 137001555 single base substitution A C upstream_gene_variant SKCA-BR 9 137002789 137002789 insertion of <=200bp - CAA intron_variant SKCA-BR 9 137002789 137002789 insertion of <=200bp - CAA upstream_gene_variant SKCA-BR 9 137004814 137004814 single base substitution G A intron_variant SKCA-BR 9 137004814 137004814 single base substitution G A upstream_gene_variant SKCA-BR 9 137005051 137005051 single base substitution A C missense_variant T18P 52A>C SKCA-BR 9 137010222 137010222 insertion of <=200bp - TTTG downstream_gene_variant SKCA-BR 9 137010222 137010222 insertion of <=200bp - TTTG intron_variant SKCA-BR 9 137013019 137013019 single base substitution T G intron_variant SKCA-BR 9 137014665 137014665 single base substitution C T intron_variant SKCA-BR 9 137016519 137016519 single base substitution C T intron_variant SKCA-BR 9 137017876 137017876 single base substitution C T intron_variant SKCA-BR 9 137019511 137019511 single base substitution T C intron_variant SKCA-BR 9 137020039 137020039 single base substitution T C intron_variant SKCA-BR 9 137020222 137020222 single base substitution C T intron_variant SKCA-BR 9 137022290 137022290 single base substitution C T intron_variant SKCA-BR 9 137023313 137023313 single base substitution T G 3_prime_UTR_variant SKCA-BR 9 137023539 137023539 single base substitution A T 3_prime_UTR_variant SKCA-BR 9 137023601 137023601 single base substitution T C 3_prime_UTR_variant SKCA-BR 9 137024615 137024615 single base substitution C T 3_prime_UTR_variant SKCA-BR 9 137024676 137024676 single base substitution T G 3_prime_UTR_variant SKCA-BR 9 137025818 137025818 single base substitution T A downstream_gene_variant SKCA-BR 9 137025819 137025819 single base substitution A G downstream_gene_variant SKCA-BR 9 137026261 137026261 single base substitution T C downstream_gene_variant SKCA-BR 9 137026511 137026512 deletion of <=200bp GT - downstream_gene_variant SKCA-BR 9 137026740 137026740 single base substitution C T downstream_gene_variant SKCA-BR 9 137028462 137028462 single base substitution A C downstream_gene_variant SKCA-BR 9 137028495 137028495 single base substitution G A downstream_gene_variant SKCA-BR 9 137029774 137029774 single base substitution G A downstream_gene_variant SKCA-BR 9 137029881 137029881 single base substitution C T downstream_gene_variant SKCM-US 9 137007496 137007496 single base substitution C T downstream_gene_variant SKCM-US 9 137007496 137007496 single base substitution C T synonymous_variant V132V 396C>T SKCM-US 9 137007825 137007825 single base substitution C T downstream_gene_variant SKCM-US 9 137007825 137007825 single base substitution C T missense_variant S171L 512C>T STAD-US 9 137005059 137005059 single base substitution G A synonymous_variant S20S 60G>A STAD-US 9 137007762 137007762 single base substitution A G downstream_gene_variant STAD-US 9 137007762 137007762 single base substitution A G missense_variant D150G 449A>G STAD-US 9 137007769 137007769 single base substitution C T downstream_gene_variant STAD-US 9 137007769 137007769 single base substitution C T synonymous_variant S152S 456C>T STAD-US 9 137019598 137019598 deletion of <=200bp C - frameshift_variant N214 STAD-US 9 137019598 137019598 insertion of <=200bp - C frameshift_variant N214N? STAD-US 9 137023052 137023054 deletion of <=200bp CAT - inframe_deletion NI314N THCA-SA 9 137005023 137005023 single base substitution C T synonymous_variant P8P 24C>T THCA-SA 9 137023952 137023952 single base substitution T C 3_prime_UTR_variant THCA-SA 9 137023979 137023979 single base substitution G A 3_prime_UTR_variant THCA-SA 9 137024067 137024067 single base substitution C T 3_prime_UTR_variant THCA-SA 9 137024248 137024248 single base substitution G C 3_prime_UTR_variant UCEC-US 9 137005034 137005034 single base substitution C G missense_variant A12G 35C>G UCEC-US 9 137007080 137007080 single base substitution G A downstream_gene_variant UCEC-US 9 137007080 137007080 single base substitution G A missense_variant D92N 274G>A UCEC-US 9 137019587 137019587 single base substitution G T splice_acceptor_variant UCEC-US 9 137019605 137019605 single base substitution G A missense_variant V217M 649G>A UCEC-US 9 137020841 137020841 single base substitution G A synonymous_variant K256K 768G>A UCEC-US 9 137021645 137021645 single base substitution A G synonymous_variant S278S 834A>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-29-T COSM4557174 c.717G>A p.K239K Substitution - coding silent 9:134155349-134155349 + PD13302a COSM5796161 c.905-8G>A p.? Unknown 9:134157885-134157885 + PTC-10C COSM4163513 c.951C>G p.A317A Substitution - coding silent 9:134157939-134157939 + HCT-116 COSM1674944 c.778T>C p.Y260H Substitution - Missense 9:134155729-134155729 + 587224 COSM1232606 c.586C>T p.R196C Substitution - Missense 9:134151984-134151984 + TCGA-OL-A66I-01 COSM3847994 c.546T>C p.D182D Substitution - coding silent 9:134148305-134148305 + CRC-06T COSM5457444 c.9G>A p.T3T Substitution - coding silent 9:134139886-134139886 + TCGA-D1-A17F-01 COSM1106569 c.675C>T p.N225N Substitution - coding silent 9:134154509-134154509 + TCGA-F4-6570-01 COSM1460902 c.450C>T p.D150D Substitution - coding silent 9:134142641-134142641 + T2269 COSM4557174 c.717G>A p.K239K Substitution - coding silent 9:134155349-134155349 + S01873 COSM5672397 c.672G>A p.P224P Substitution - coding silent 9:134154506-134154506 + C0083T COSM4138885 c.515A>C p.D172A Substitution - Missense 9:134142706-134142706 + TCGA-A8-A06Z-01 COSM455564 c.846T>A p.L282L Substitution - coding silent 9:134156535-134156535 + 12-P616 COSM4588562 c.80A>G p.K27R Substitution - Missense 9:134139957-134139957 + LS411 COSM1460904 c.641_642insC p.V217fs*42 Insertion - Frameshift 9:134154475-134154476 + CSCC-40-T COSM1460905 c.642delC p.V217fs*4 Deletion - Frameshift 9:134154476-134154476 + Pat_40_B COSM5875800 c.427C>T p.L143F Substitution - Missense 9:134142405-134142405 + TCGA-AU-6004-01 COSM1460905 c.642delC p.V217fs*4 Deletion - Frameshift 9:134154476-134154476 + ESO-0029 COSM1270407 c.636C>T p.D212D Substitution - coding silent 9:134154470-134154470 + TCGA-F4-6809-01 COSM1460906 c.874G>C p.E292Q Substitution - Missense 9:134156563-134156563 + LN229 COSM3214183 c.736G>A p.G246R Substitution - Missense 9:134155368-134155368 + HCT116 COSM1674944 c.778T>C p.Y260H Substitution - Missense 9:134155729-134155729 + TCGA-EE-A3AC-06 COSM3655418 c.512C>T p.S171L Substitution - Missense 9:134142703-134142703 + BD124T COSM5492599 c.600C>T p.T200T Substitution - coding silent 9:134151998-134151998 + SNUH_G73_S1 COSM4415607 c.150C>T p.S50S Substitution - coding silent 9:134140771-134140771 + T3262 COSM3905440 c.456C>T p.S152S Substitution - coding silent 9:134142647-134142647 + RKO COSM1460904 c.641_642insC p.V217fs*42 Insertion - Frameshift 9:134154475-134154476 + TCGA-B5-A11G-01 COSM1106568 c.649G>A p.V217M Substitution - Missense 9:134154483-134154483 + CRC-35T COSM5468848 c.246C>T p.T82T Substitution - coding silent 9:134141565-134141565 + PT46 COSM5929159 c.529-4C>T p.? Unknown 9:134148284-134148284 + TCGA-BH-A18G-01 COSM5218330 c.9_11delGGA p.E5delE Deletion - In frame 9:134139886-134139888 + PT35 COSM5912984 c.647C>T p.P216L Substitution - Missense 9:134154481-134154481 + Gp5D COSM1460904 c.641_642insC p.V217fs*42 Insertion - Frameshift 9:134154475-134154476 + Pat_41_B COSM5875799 c.71C>T p.T24I Substitution - Missense 9:134139948-134139948 + Gp2D COSM1460904 c.641_642insC p.V217fs*42 Insertion - Frameshift 9:134154475-134154476 + PTC-28C COSM4163512 c.911T>G p.V304G Substitution - Missense 9:134157899-134157899 + TCGA-CJ-5680-01 COSM3367629 c.222G>A p.A74A Substitution - coding silent 9:134141541-134141541 + TCGA-AX-A05Z-01 COSM1106566 c.274G>A p.D92N Substitution - Missense 9:134141958-134141958 + TCGA-AP-A0LM-01 COSM1106567 c.632-1G>T p.? Unknown 9:134154465-134154465 + TCGA-AN-A0FY-01 COSM1460904 c.641_642insC p.V217fs*42 Insertion - Frameshift 9:134154475-134154476 + TCGA-D5-6538-01 COSM1460903 c.529-2A>G p.? Unknown 9:134148286-134148286 + LS174T COSM1460905 c.642delC p.V217fs*4 Deletion - Frameshift 9:134154476-134154476 + Pat_06_A COSM1460905 c.642delC p.V217fs*4 Deletion - Frameshift 9:134154476-134154476 + TCGA-CG-5718-01 COSM3905439 c.449A>G p.D150G Substitution - Missense 9:134142640-134142640 + TCGA-AP-A0LM-01 COSM1106570 c.768G>A p.K256K Substitution - coding silent 9:134155719-134155719 + TCGA-B5-A11E-01 COSM1106565 c.35C>G p.A12G Substitution - Missense 9:134139912-134139912 + YULAPE COSM1701905 c.443_444CC>TT p.S148F Substitution - Missense 9:134142421-134142422 + TCGA-FW-A3R5-06 COSM3926398 c.396C>T p.V132V Substitution - coding silent 9:134142374-134142374 + HCC32T COSM3664211 c.4G>C p.A2P Substitution - Missense 9:134139881-134139881 + TCGA-BS-A0UJ-01 COSM1106571 c.834A>G p.S278S Substitution - coding silent 9:134156523-134156523 + U2940 COSM5622169 c.223T>C p.Y75H Substitution - Missense 9:134141542-134141542 + 2334187 COSM324301 c.555G>C p.L185F Substitution - Missense 9:134148314-134148314 + T1154 COSM4740983 c.775A>T p.K259* Substitution - Nonsense 9:134155726-134155726 + TCGA-B0-5695-01 COSM487199 c.845T>C p.L282P Substitution - Missense 9:134156534-134156534 + BD114T COSM5503561 c.54C>T p.T18T Substitution - coding silent 9:134139931-134139931 + TCGA-G4-6309-01 COSM1460905 c.642delC p.V217fs*4 Deletion - Frameshift 9:134154476-134154476 + PTC-54C COSM4163511 c.24C>T p.P8P Substitution - coding silent 9:134139901-134139901 + TCGA-BR-A4QL-01 COSM3905438 c.60G>A p.S20S Substitution - coding silent 9:134139937-134139937 + PT13 COSM5896030 c.670C>T p.P224S Substitution - Missense 9:134154504-134154504 + H1155 COSM1195666 c.601G>A p.A201T Substitution - Missense 9:134151999-134151999 + LOVO COSM3214184 c.830G>A p.G277D Substitution - Missense 9:134156519-134156519 + HCC32 COSM3664211 c.4G>C p.A2P Substitution - Missense 9:134139881-134139881 + 2521243 COSM5886652 c.528+8C>T p.? Unknown 9:134142727-134142727 + PD9569a COSM5769583 c.708-6T>C p.? Unknown 9:134155334-134155334 + TCGA-B0-5712-01 COSM1497024 c.399T>G p.F133L Substitution - Missense 9:134142377-134142377 + TCGA-HU-A4G8-01 COSM3905440 c.456C>T p.S152S Substitution - coding silent 9:134142647-134142647 + PT48 COSM3214182 c.653C>T p.S218F Substitution - Missense 9:134154487-134154487 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.397638 9q34 609012

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G 3-UTRSNV . c.1002+277A>G 9 137023389 HC A G Missense p.D150G c.449A>G 9 137007762 STAD A G Missense p.Y35C c.104A>G 9 137005847 LGG A T SpliceAcceptorSNV . c.265-2A>T 9 137007069 BRCA C T Missense p.S171L c.512C>T 9 137007825 CM C T Missense p.S202L c.605C>T 9 137017125 LUAD C T Synonymous p.D212D c.636C>T 9 137019592 ESCA C T Synonymous p.S148S c.444C>T 9 137007544 CM G A Missense p.D199N c.595G>A 9 137017115 CM G A Missense p.G147E c.440G>A 9 137007540 RCCC G A Missense p.S62N c.185G>A 9 137005928 CM G A Missense p.V217M c.649G>A 9 137019605 UCEC G A Nonsense p.W198* c.593G>A 9 137017113 HNSC G A Synonymous p.A74A c.222G>A 9 137006663 RCCC G C Missense p.E9D c.27G>C 9 137005026 HNSC G C Missense p.L185F c.555G>C 9 137013436 SCLC T A Synonymous p.L282L c.846T>A 9 137021657 BRCA