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 ACC 9 131418828 131418828 + Missense_Mutation SNP A A C TCGA-OR-A5JD-01A-11D-A29I-10 TCGA-OR-A5JD-10B-01D-A29L-10 g.chr9:131418828A>C c.178T>G c.(178-180)Tgg>Ggg p.W60G ACC 9 131418828 131418828 + Missense_Mutation SNP A A C TCGA-OR-A5JK-01A-11D-A29I-10 TCGA-OR-A5JK-10A-01D-A29L-10 g.chr9:131418828A>C c.178T>G c.(178-180)Tgg>Ggg p.W60G ACC 9 131418828 131418828 + Missense_Mutation SNP A A C TCGA-OR-A5JP-01A-11D-A29I-10 TCGA-OR-A5JP-10A-01D-A29L-10 g.chr9:131418828A>C c.178T>G c.(178-180)Tgg>Ggg p.W60G ACC 9 131418828 131418828 + Missense_Mutation SNP A A C TCGA-OR-A5LD-01A-11D-A29I-10 TCGA-OR-A5LD-10A-01D-A29L-10 g.chr9:131418828A>C c.178T>G c.(178-180)Tgg>Ggg p.W60G ACC 9 131418828 131418828 + Missense_Mutation SNP A A C TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr9:131418828A>C c.178T>G c.(178-180)Tgg>Ggg p.W60G BLCA 9 131396190 131396190 + Nonsense_Mutation SNP C C A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr9:131396190C>A c.1444G>T c.(1444-1446)Gaa>Taa p.E482* BLCA 9 131396209 131396209 + Missense_Mutation SNP C C G TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:131396209C>G c.1425G>C c.(1423-1425)ttG>ttC p.L475F BLCA 9 131396647 131396647 + Silent SNP G G A TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr9:131396647G>A c.1230C>T c.(1228-1230)agC>agT p.S410S BLCA 9 131397156 131397156 + Silent SNP G G A TCGA-BT-A42C-01A-11D-A23M-08 TCGA-BT-A42C-10A-01D-A23K-08 g.chr9:131397156G>A c.1026C>T c.(1024-1026)ttC>ttT p.F342F BLCA 9 131397988 131397988 + Silent SNP C C A TCGA-GV-A3JW-01A-11D-A20D-08 TCGA-GV-A3JW-10A-01D-A20D-08 g.chr9:131397988C>A c.762G>T c.(760-762)ctG>ctT p.L254L BLCA 9 131403068 131403068 + Missense_Mutation SNP G G A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr9:131403068G>A c.337C>T c.(337-339)Cgg>Tgg p.R113W BRCA 9 131397466 131397466 + Silent SNP G G A TCGA-E9-A1RB-01A-11D-A17G-09 TCGA-E9-A1RB-10A-01D-A159-09 g.chr9:131397466G>A c.886C>T c.(886-888)Cta>Tta p.L296L BRCA 9 131403095 131403095 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:131403095C>T c.310G>A c.(310-312)Gac>Aac p.D104N CHOL 9 131396553 131396553 + Missense_Mutation SNP G G A TCGA-3X-AAVC-01A-21D-A417-09 TCGA-3X-AAVC-10A-01D-A41A-09 g.chr9:131396553G>A c.1324C>T c.(1324-1326)Cgc>Tgc p.R442C COAD 9 131396151 131396151 + Missense_Mutation SNP T T C TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr9:131396151T>C c.1483A>G c.(1483-1485)Act>Gct p.T495A COAD 9 131396553 131396553 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:131396553G>A c.1324C>T c.(1324-1326)Cgc>Tgc p.R442C COAD 9 131397114 131397114 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr9:131397114G>A c.1068C>T c.(1066-1068)ggC>ggT p.G356G COAD 9 131397431 131397431 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:131397431C>T c.921G>A c.(919-921)caG>caA p.Q307Q COADREAD 9 131396151 131396151 + Missense_Mutation SNP T T C TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr9:131396151T>C c.1483A>G c.(1483-1485)Act>Gct p.T495A COADREAD 9 131396553 131396553 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:131396553G>A c.1324C>T c.(1324-1326)Cgc>Tgc p.R442C COADREAD 9 131397114 131397114 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr9:131397114G>A c.1068C>T c.(1066-1068)ggC>ggT p.G356G COADREAD 9 131397431 131397431 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:131397431C>T c.921G>A c.(919-921)caG>caA p.Q307Q DLBC 9 131398633 131398633 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr9:131398633C>T c.630G>A c.(628-630)ccG>ccA p.P210P ESCA 9 131403128 131403128 + Missense_Mutation SNP C C T TCGA-L5-A8NG-01A-11D-A37C-09 TCGA-L5-A8NG-11A-11D-A37F-09 g.chr9:131403128C>T c.277G>A c.(277-279)Gtg>Atg p.V93M ESCA 9 131403138 131403138 + Silent SNP C C T TCGA-L5-A8NR-01A-11D-A37C-09 TCGA-L5-A8NR-11A-11D-A37F-09 g.chr9:131403138C>T c.267G>A c.(265-267)acG>acA p.T89T HNSC 9 131396030 131396030 + Missense_Mutation SNP G G A TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr9:131396030G>A c.1604C>T c.(1603-1605)gCg>gTg p.A535V HNSC 9 131396039 131396039 + Missense_Mutation SNP G G T TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr9:131396039G>T c.1595C>A c.(1594-1596)gCa>gAa p.A532E HNSC 9 131397505 131397505 + Missense_Mutation SNP G G A TCGA-HD-7229-01A-11D-2012-08 TCGA-HD-7229-10A-01D-2013-08 g.chr9:131397505G>A c.847C>T c.(847-849)Cgc>Tgc p.R283C LUAD 9 131396070 131396070 + Missense_Mutation SNP G G A TCGA-05-4420-01A-01D-1265-08 TCGA-05-4420-10A-01D-1265-08 g.chr9:131396070G>A c.1564C>T c.(1564-1566)Cgg>Tgg p.R522W LUAD 9 131398630 131398630 + Silent SNP C C T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr9:131398630C>T c.633G>A c.(631-633)tcG>tcA p.S211S LUAD 9 131403138 131403138 + Silent SNP C C T TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr9:131403138C>T c.267G>A c.(265-267)acG>acA p.T89T LUSC 9 131396147 131396147 + Missense_Mutation SNP T T C TCGA-66-2783-01A-01D-1267-08 TCGA-66-2783-11A-01D-1267-08 g.chr9:131396147T>C c.1487A>G c.(1486-1488)cAg>cGg p.Q496R LUSC 9 131396538 131396538 + Missense_Mutation SNP G G A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr9:131396538G>A c.1339C>T c.(1339-1341)Cgg>Tgg p.R447W PAAD 9 131396214 131396214 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:131396214C>A c.1420G>T c.(1420-1422)Gtt>Ttt p.V474F PAAD 9 131397074 131397074 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:131397074C>T c.1108G>A c.(1108-1110)Gcc>Acc p.A370T PAAD 9 131397201 131397201 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:131397201C>A c.e7-1 SKCM 9 131396564 131396564 + Missense_Mutation SNP A A T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr9:131396564A>T c.1313T>A c.(1312-1314)cTg>cAg p.L438Q SKCM 9 131397188 131397188 + Missense_Mutation SNP C C T TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr9:131397188C>T c.994G>A c.(994-996)Gag>Aag p.E332K SKCM 9 131398016 131398016 + Nonsense_Mutation SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr9:131398016C>T c.734G>A c.(733-735)tGg>tAg p.W245* SKCM 9 131418973 131418973 + Silent SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr9:131418973G>A c.33C>T c.(31-33)agC>agT p.S11S

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 131394424 131394424 single base substitution C T downstream_gene_variant BLCA-CN 9 131397479 131397479 single base substitution G A downstream_gene_variant BLCA-CN 9 131397479 131397479 single base substitution G A exon_variant BLCA-CN 9 131397479 131397479 single base substitution G A synonymous_variant T291T 873C>T BLCA-US 9 131392643 131392643 single base substitution G A downstream_gene_variant BLCA-US 9 131394948 131394948 single base substitution G A downstream_gene_variant BLCA-US 9 131395126 131395126 single base substitution G A downstream_gene_variant BLCA-US 9 131396209 131396209 single base substitution C G downstream_gene_variant BLCA-US 9 131396209 131396209 single base substitution C G missense_variant L475F 1425G>C BLCA-US 9 131396647 131396647 single base substitution G A downstream_gene_variant BLCA-US 9 131396647 131396647 single base substitution G A synonymous_variant S410S 1230C>T BLCA-US 9 131397156 131397156 single base substitution G A downstream_gene_variant BLCA-US 9 131397156 131397156 single base substitution G A exon_variant BLCA-US 9 131397156 131397156 single base substitution G A synonymous_variant F342F 1026C>T BLCA-US 9 131397988 131397988 single base substitution C A downstream_gene_variant BLCA-US 9 131397988 131397988 single base substitution C A exon_variant BLCA-US 9 131397988 131397988 single base substitution C A synonymous_variant L254L 762G>T BRCA-EU 9 131392257 131392257 single base substitution A G downstream_gene_variant BRCA-EU 9 131392277 131392277 single base substitution C T downstream_gene_variant BRCA-EU 9 131392347 131392347 single base substitution G A downstream_gene_variant BRCA-EU 9 131392528 131392528 single base substitution G C downstream_gene_variant BRCA-EU 9 131392811 131392811 single base substitution C T downstream_gene_variant BRCA-EU 9 131395657 131395657 single base substitution G A downstream_gene_variant BRCA-EU 9 131396425 131396425 single base substitution C G downstream_gene_variant BRCA-EU 9 131396425 131396425 single base substitution C G intron_variant BRCA-EU 9 131397475 131397475 single base substitution C T downstream_gene_variant BRCA-EU 9 131397475 131397475 single base substitution C T exon_variant BRCA-EU 9 131397475 131397475 single base substitution C T missense_variant G293R 877G>A BRCA-EU 9 131399677 131399677 single base substitution C T intron_variant BRCA-EU 9 131399677 131399677 single base substitution C T upstream_gene_variant BRCA-EU 9 131403205 131403205 single base substitution G A exon_variant BRCA-EU 9 131403205 131403205 single base substitution G A missense_variant T52M 155C>T BRCA-EU 9 131403205 131403205 single base substitution G A missense_variant T58M 173C>T BRCA-EU 9 131403205 131403205 single base substitution G A missense_variant T67M 200C>T BRCA-EU 9 131403205 131403205 single base substitution G A upstream_gene_variant BRCA-EU 9 131405033 131405033 single base substitution C T intron_variant BRCA-EU 9 131405169 131405169 insertion of <=200bp - A intron_variant BRCA-EU 9 131406105 131406105 single base substitution G C intron_variant BRCA-EU 9 131406460 131406460 single base substitution A T intron_variant BRCA-EU 9 131408871 131408871 single base substitution G A intron_variant BRCA-EU 9 131411841 131411841 single base substitution G A intron_variant BRCA-EU 9 131415115 131415115 single base substitution T A intron_variant BRCA-EU 9 131415141 131415141 single base substitution G A intron_variant BRCA-EU 9 131415426 131415426 single base substitution T A intron_variant BRCA-EU 9 131416128 131416128 single base substitution A G intron_variant BRCA-EU 9 131416217 131416217 single base substitution G C intron_variant BRCA-EU 9 131417863 131417863 single base substitution G T intron_variant BRCA-EU 9 131418327 131418327 single base substitution A T intron_variant BRCA-EU 9 131418549 131418549 single base substitution C T intron_variant BRCA-EU 9 131419352 131419352 single base substitution C T upstream_gene_variant BRCA-EU 9 131420215 131420215 insertion of <=200bp - T upstream_gene_variant BRCA-EU 9 131421675 131421675 single base substitution G A upstream_gene_variant BRCA-EU 9 131421751 131421751 single base substitution G C upstream_gene_variant BRCA-EU 9 131422458 131422458 single base substitution G A upstream_gene_variant BRCA-EU 9 131422709 131422709 single base substitution A T upstream_gene_variant BRCA-EU 9 131422901 131422901 single base substitution C G upstream_gene_variant BRCA-EU 9 131423099 131423099 single base substitution C G upstream_gene_variant BRCA-EU 9 131423674 131423674 single base substitution G A upstream_gene_variant BRCA-FR 9 131397475 131397475 single base substitution C T downstream_gene_variant BRCA-FR 9 131397475 131397475 single base substitution C T exon_variant BRCA-FR 9 131397475 131397475 single base substitution C T missense_variant G293R 877G>A BRCA-FR 9 131406105 131406105 single base substitution G C intron_variant BRCA-FR 9 131408871 131408871 single base substitution G A intron_variant BRCA-FR 9 131421751 131421751 single base substitution G C upstream_gene_variant BRCA-FR 9 131423099 131423099 single base substitution C G upstream_gene_variant BRCA-KR 9 131419009 131419009 single base substitution G A 5_prime_UTR_variant BRCA-KR 9 131419009 131419009 single base substitution G A upstream_gene_variant BRCA-UK 9 131395124 131395124 single base substitution A G downstream_gene_variant BRCA-UK 9 131404816 131404816 single base substitution G A intron_variant BRCA-UK 9 131415426 131415426 single base substitution T A intron_variant BRCA-UK 9 131419486 131419486 single base substitution C T upstream_gene_variant BRCA-US 9 131394575 131394575 single base substitution A G downstream_gene_variant BRCA-US 9 131397466 131397466 single base substitution G A downstream_gene_variant BRCA-US 9 131397466 131397466 single base substitution G A exon_variant BRCA-US 9 131397466 131397466 single base substitution G A synonymous_variant L296L 886C>T BRCA-US 9 131403095 131403095 single base substitution C T exon_variant BRCA-US 9 131403095 131403095 single base substitution C T missense_variant D104N 310G>A BRCA-US 9 131403095 131403095 single base substitution C T missense_variant D89N 265G>A BRCA-US 9 131403095 131403095 single base substitution C T missense_variant D95N 283G>A BRCA-US 9 131403095 131403095 single base substitution C T upstream_gene_variant BTCA-JP 9 131394901 131394901 single base substitution C G downstream_gene_variant BTCA-JP 9 131396217 131396217 single base substitution T G downstream_gene_variant BTCA-JP 9 131396217 131396217 single base substitution T G missense_variant T473P 1417A>C BTCA-JP 9 131398122 131398122 single base substitution C T downstream_gene_variant BTCA-JP 9 131398122 131398122 single base substitution C T exon_variant BTCA-JP 9 131398122 131398122 single base substitution C T intron_variant BTCA-JP 9 131398633 131398633 single base substitution C T 3_prime_UTR_variant BTCA-JP 9 131398633 131398633 single base substitution C T exon_variant BTCA-JP 9 131398633 131398633 single base substitution C T synonymous_variant P201P 603G>A BTCA-JP 9 131398633 131398633 single base substitution C T synonymous_variant P210P 630G>A BTCA-JP 9 131398633 131398633 single base substitution C T upstream_gene_variant CESC-US 9 131395165 131395165 single base substitution G A downstream_gene_variant CESC-US 9 131395181 131395181 single base substitution C T downstream_gene_variant CLLE-ES 9 131413796 131413796 single base substitution T A intron_variant COAD-US 9 131394910 131394910 single base substitution G A downstream_gene_variant COAD-US 9 131394992 131394992 single base substitution G A downstream_gene_variant COAD-US 9 131395091 131395091 single base substitution G T downstream_gene_variant COAD-US 9 131395517 131395517 single base substitution C G downstream_gene_variant COAD-US 9 131395553 131395553 single base substitution C T downstream_gene_variant COAD-US 9 131396553 131396553 single base substitution G A downstream_gene_variant COAD-US 9 131396553 131396553 single base substitution G A missense_variant R442C 1324C>T COAD-US 9 131397114 131397114 single base substitution G A downstream_gene_variant COAD-US 9 131397114 131397114 single base substitution G A exon_variant COAD-US 9 131397114 131397114 single base substitution G A synonymous_variant G356G 1068C>T COAD-US 9 131397431 131397431 single base substitution C T downstream_gene_variant COAD-US 9 131397431 131397431 single base substitution C T exon_variant COAD-US 9 131397431 131397431 single base substitution C T synonymous_variant Q307Q 921G>A COAD-US 9 131398636 131398636 single base substitution C T 3_prime_UTR_variant COAD-US 9 131398636 131398636 single base substitution C T exon_variant COAD-US 9 131398636 131398636 single base substitution C T synonymous_variant Q200Q 600G>A COAD-US 9 131398636 131398636 single base substitution C T synonymous_variant Q209Q 627G>A COAD-US 9 131398636 131398636 single base substitution C T upstream_gene_variant COAD-US 9 131399200 131399200 single base substitution C T exon_variant COAD-US 9 131399200 131399200 single base substitution C T intron_variant COAD-US 9 131399200 131399200 single base substitution C T missense_variant G172D 515G>A COAD-US 9 131399200 131399200 single base substitution C T missense_variant G181D 542G>A COAD-US 9 131399200 131399200 single base substitution C T upstream_gene_variant COCA-CN 9 131394561 131394561 single base substitution C T downstream_gene_variant COCA-CN 9 131395403 131395403 single base substitution G A downstream_gene_variant COCA-CN 9 131396635 131396635 single base substitution G A downstream_gene_variant COCA-CN 9 131396635 131396635 single base substitution G A synonymous_variant D414D 1242C>T COCA-CN 9 131397657 131397657 single base substitution A G downstream_gene_variant COCA-CN 9 131397657 131397657 single base substitution A G exon_variant COCA-CN 9 131397657 131397657 single base substitution A G intron_variant COCA-CN 9 131401956 131401956 single base substitution T G intron_variant COCA-CN 9 131401956 131401956 single base substitution T G upstream_gene_variant COCA-CN 9 131402182 131402182 single base substitution T G intron_variant COCA-CN 9 131402182 131402182 single base substitution T G upstream_gene_variant COCA-CN 9 131415865 131415865 single base substitution T C intron_variant ESAD-UK 9 131392226 131392226 single base substitution C G downstream_gene_variant ESAD-UK 9 131393256 131393256 single base substitution G A downstream_gene_variant ESAD-UK 9 131395916 131395916 single base substitution A G downstream_gene_variant ESAD-UK 9 131395956 131395956 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 131395956 131395956 single base substitution C T downstream_gene_variant ESAD-UK 9 131396227 131396227 single base substitution G T downstream_gene_variant ESAD-UK 9 131396227 131396227 single base substitution G T synonymous_variant S469S 1407C>A ESAD-UK 9 131396659 131396659 single base substitution A T downstream_gene_variant ESAD-UK 9 131396659 131396659 single base substitution A T missense_variant N406K 1218T>A ESAD-UK 9 131396944 131396944 single base substitution G A downstream_gene_variant ESAD-UK 9 131396944 131396944 single base substitution G A intron_variant ESAD-UK 9 131400602 131400602 single base substitution C A intron_variant ESAD-UK 9 131400602 131400602 single base substitution C A upstream_gene_variant ESAD-UK 9 131400980 131400980 single base substitution C T intron_variant ESAD-UK 9 131400980 131400980 single base substitution C T upstream_gene_variant ESAD-UK 9 131401946 131401946 deletion of <=200bp T - intron_variant ESAD-UK 9 131401946 131401946 deletion of <=200bp T - upstream_gene_variant ESAD-UK 9 131404950 131404950 single base substitution C T intron_variant ESAD-UK 9 131405129 131405129 single base substitution C T intron_variant ESAD-UK 9 131405538 131405538 single base substitution G C intron_variant ESAD-UK 9 131405560 131405560 single base substitution C T intron_variant ESAD-UK 9 131406057 131406057 single base substitution G A intron_variant ESAD-UK 9 131408207 131408207 single base substitution C G intron_variant ESAD-UK 9 131416049 131416049 single base substitution G A intron_variant ESAD-UK 9 131416073 131416073 single base substitution G A intron_variant ESAD-UK 9 131419187 131419187 single base substitution A G upstream_gene_variant ESAD-UK 9 131419849 131419849 single base substitution A C upstream_gene_variant ESAD-UK 9 131422488 131422488 single base substitution C T upstream_gene_variant ESAD-UK 9 131423514 131423514 single base substitution C T upstream_gene_variant ESCA-CN 9 131397479 131397479 single base substitution G A downstream_gene_variant ESCA-CN 9 131397479 131397479 single base substitution G A exon_variant ESCA-CN 9 131397479 131397479 single base substitution G A synonymous_variant T291T 873C>T GBM-US 9 131395212 131395212 single base substitution T A downstream_gene_variant KIRP-US 9 131394992 131394992 single base substitution G A downstream_gene_variant LAML-KR 9 131398409 131398409 single base substitution G A 3_prime_UTR_variant LAML-KR 9 131398409 131398409 single base substitution G A intron_variant LAML-KR 9 131398409 131398409 single base substitution G A upstream_gene_variant LAML-KR 9 131418147 131418147 single base substitution G A intron_variant LAML-KR 9 131418225 131418225 single base substitution A G intron_variant LICA-CN 9 131396142 131396142 single base substitution A C downstream_gene_variant LICA-CN 9 131396142 131396142 single base substitution A C missense_variant L498V 1492T>G LICA-CN 9 131397185 131397185 single base substitution T C downstream_gene_variant LICA-CN 9 131397185 131397185 single base substitution T C exon_variant LICA-CN 9 131397185 131397185 single base substitution T C missense_variant T333A 997A>G LICA-FR 9 131395509 131395509 single base substitution G T downstream_gene_variant LICA-FR 9 131397127 131397127 single base substitution A G downstream_gene_variant LICA-FR 9 131397127 131397127 single base substitution A G exon_variant LICA-FR 9 131397127 131397127 single base substitution A G missense_variant L352P 1055T>C LICA-FR 9 131397375 131397375 single base substitution T C downstream_gene_variant LICA-FR 9 131397375 131397375 single base substitution T C exon_variant LICA-FR 9 131397375 131397375 single base substitution T C missense_variant K326R 977A>G LICA-FR 9 131400500 131400500 deletion of <=200bp A - intron_variant LICA-FR 9 131400500 131400500 deletion of <=200bp A - upstream_gene_variant LICA-FR 9 131422343 131422343 single base substitution C A upstream_gene_variant LINC-JP 9 131392721 131392721 single base substitution C A downstream_gene_variant LINC-JP 9 131395164 131395164 single base substitution A G downstream_gene_variant LINC-JP 9 131395172 131395172 single base substitution A T downstream_gene_variant LINC-JP 9 131395698 131395698 deletion of <=200bp A - downstream_gene_variant LINC-JP 9 131412117 131412117 single base substitution C T intron_variant LINC-JP 9 131418459 131418459 single base substitution A G intron_variant LINC-JP 9 131421421 131421421 single base substitution C T upstream_gene_variant LIRI-JP 9 131392402 131392402 single base substitution T G downstream_gene_variant LIRI-JP 9 131394297 131394297 single base substitution A T downstream_gene_variant LIRI-JP 9 131395250 131395250 single base substitution G A downstream_gene_variant LIRI-JP 9 131401954 131401954 single base substitution T C intron_variant LIRI-JP 9 131401954 131401954 single base substitution T C upstream_gene_variant LIRI-JP 9 131405285 131405285 single base substitution T C intron_variant LIRI-JP 9 131408652 131408652 single base substitution T C intron_variant LIRI-JP 9 131411343 131411343 single base substitution C A intron_variant LIRI-JP 9 131411667 131411667 single base substitution A T intron_variant LIRI-JP 9 131412299 131412299 single base substitution A C intron_variant LIRI-JP 9 131414895 131414895 single base substitution T A intron_variant LIRI-JP 9 131417339 131417339 single base substitution C T intron_variant LIRI-JP 9 131418532 131418532 single base substitution G C intron_variant LIRI-JP 9 131423504 131423504 single base substitution C T upstream_gene_variant LIRI-JP 9 131424027 131424028 deletion of <=200bp TG - upstream_gene_variant LUSC-KR 9 131397479 131397479 single base substitution G A downstream_gene_variant LUSC-KR 9 131397479 131397479 single base substitution G A exon_variant LUSC-KR 9 131397479 131397479 single base substitution G A synonymous_variant T291T 873C>T LUSC-KR 9 131402305 131402305 single base substitution G T intron_variant LUSC-KR 9 131402305 131402305 single base substitution G T upstream_gene_variant LUSC-KR 9 131407537 131407537 single base substitution G C intron_variant LUSC-KR 9 131414747 131414747 single base substitution C A intron_variant LUSC-KR 9 131423603 131423603 single base substitution C A upstream_gene_variant LUSC-US 9 131396147 131396147 single base substitution T C downstream_gene_variant LUSC-US 9 131396147 131396147 single base substitution T C missense_variant Q496R 1487A>G LUSC-US 9 131396538 131396538 single base substitution G A downstream_gene_variant LUSC-US 9 131396538 131396538 single base substitution G A missense_variant R447W 1339C>T MALY-DE 9 131407201 131407201 single base substitution C T intron_variant MELA-AU 9 131391077 131391077 single base substitution C T downstream_gene_variant MELA-AU 9 131391462 131391462 single base substitution G A downstream_gene_variant MELA-AU 9 131391476 131391476 single base substitution C T downstream_gene_variant MELA-AU 9 131391653 131391653 single base substitution C A downstream_gene_variant MELA-AU 9 131391899 131391899 single base substitution C T downstream_gene_variant MELA-AU 9 131392411 131392412 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 131394197 131394197 single base substitution A G downstream_gene_variant MELA-AU 9 131394781 131394781 single base substitution C A downstream_gene_variant MELA-AU 9 131395180 131395180 single base substitution C T downstream_gene_variant MELA-AU 9 131395507 131395508 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 9 131395563 131395564 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 9 131395761 131395761 single base substitution C T downstream_gene_variant MELA-AU 9 131396215 131396216 deletion of <=200bp TG - downstream_gene_variant MELA-AU 9 131396215 131396216 deletion of <=200bp TG - frameshift_variant T473 MELA-AU 9 131397559 131397559 single base substitution G A downstream_gene_variant MELA-AU 9 131397559 131397559 single base substitution G A intron_variant MELA-AU 9 131398522 131398522 single base substitution C T 3_prime_UTR_variant MELA-AU 9 131398522 131398522 single base substitution C T intron_variant MELA-AU 9 131398522 131398522 single base substitution C T synonymous_variant R238R 714G>A MELA-AU 9 131398522 131398522 single base substitution C T upstream_gene_variant MELA-AU 9 131400135 131400135 single base substitution G A intron_variant MELA-AU 9 131400135 131400135 single base substitution G A upstream_gene_variant MELA-AU 9 131401451 131401451 single base substitution G A intron_variant MELA-AU 9 131401451 131401451 single base substitution G A upstream_gene_variant MELA-AU 9 131401994 131401994 single base substitution G T intron_variant MELA-AU 9 131401994 131401994 single base substitution G T upstream_gene_variant MELA-AU 9 131403068 131403068 single base substitution G A exon_variant MELA-AU 9 131403068 131403068 single base substitution G A missense_variant R104W 310C>T MELA-AU 9 131403068 131403068 single base substitution G A missense_variant R113W 337C>T MELA-AU 9 131403068 131403068 single base substitution G A missense_variant R98W 292C>T MELA-AU 9 131403068 131403068 single base substitution G A upstream_gene_variant MELA-AU 9 131403522 131403522 single base substitution G A intron_variant MELA-AU 9 131403522 131403522 single base substitution G A upstream_gene_variant MELA-AU 9 131403999 131403999 single base substitution C T intron_variant MELA-AU 9 131403999 131403999 single base substitution C T upstream_gene_variant MELA-AU 9 131404667 131404668 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 131406060 131406060 single base substitution C T intron_variant MELA-AU 9 131406448 131406448 single base substitution G A intron_variant MELA-AU 9 131406541 131406541 single base substitution G A intron_variant MELA-AU 9 131406804 131406804 single base substitution C G intron_variant MELA-AU 9 131406812 131406812 single base substitution C T intron_variant MELA-AU 9 131407369 131407369 single base substitution C G intron_variant MELA-AU 9 131407414 131407414 single base substitution G A intron_variant MELA-AU 9 131407548 131407548 single base substitution G A intron_variant MELA-AU 9 131408622 131408622 single base substitution G A intron_variant MELA-AU 9 131408916 131408916 single base substitution C G intron_variant MELA-AU 9 131409279 131409279 single base substitution C T intron_variant MELA-AU 9 131409797 131409797 single base substitution G A intron_variant MELA-AU 9 131410392 131410392 single base substitution G A intron_variant MELA-AU 9 131410764 131410764 single base substitution A G intron_variant MELA-AU 9 131411211 131411211 single base substitution G A intron_variant MELA-AU 9 131411354 131411354 single base substitution G A intron_variant MELA-AU 9 131411590 131411590 single base substitution G A intron_variant MELA-AU 9 131411624 131411624 single base substitution G A intron_variant MELA-AU 9 131411941 131411941 single base substitution C T intron_variant MELA-AU 9 131414191 131414191 single base substitution C T intron_variant MELA-AU 9 131414687 131414687 single base substitution G A intron_variant MELA-AU 9 131415520 131415520 single base substitution G A intron_variant MELA-AU 9 131415762 131415762 single base substitution G A intron_variant MELA-AU 9 131417143 131417143 single base substitution C T intron_variant MELA-AU 9 131418675 131418675 single base substitution T A intron_variant MELA-AU 9 131418932 131418932 single base substitution C T exon_variant MELA-AU 9 131418932 131418932 single base substitution C T missense_variant G10E 29G>A MELA-AU 9 131418932 131418932 single base substitution C T missense_variant G16E 47G>A MELA-AU 9 131418932 131418932 single base substitution C T missense_variant G25E 74G>A MELA-AU 9 131419104 131419104 single base substitution A G upstream_gene_variant MELA-AU 9 131420091 131420091 single base substitution A T upstream_gene_variant MELA-AU 9 131420994 131420994 single base substitution G A upstream_gene_variant MELA-AU 9 131421487 131421488 multiple base substitution (>=2bp and <=200bp) AC GT upstream_gene_variant MELA-AU 9 131421584 131421584 single base substitution C T upstream_gene_variant MELA-AU 9 131422360 131422360 single base substitution C T upstream_gene_variant MELA-AU 9 131422472 131422472 single base substitution C T upstream_gene_variant MELA-AU 9 131422478 131422478 single base substitution C T upstream_gene_variant MELA-AU 9 131423516 131423516 single base substitution G A upstream_gene_variant MELA-AU 9 131423800 131423801 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant ORCA-IN 9 131395574 131395574 single base substitution C T downstream_gene_variant ORCA-IN 9 131414644 131414644 single base substitution G C intron_variant ORCA-IN 9 131415520 131415520 single base substitution G C intron_variant ORCA-IN 9 131416807 131416807 single base substitution G A intron_variant OV-AU 9 131393535 131393535 single base substitution G A downstream_gene_variant OV-AU 9 131416760 131416760 single base substitution C G intron_variant OV-AU 9 131417976 131417976 single base substitution C A intron_variant PACA-AU 9 131394055 131394055 single base substitution C T downstream_gene_variant PACA-AU 9 131394425 131394425 single base substitution G A downstream_gene_variant PACA-AU 9 131394618 131394618 single base substitution G A downstream_gene_variant PACA-AU 9 131402429 131402429 single base substitution G T intron_variant PACA-AU 9 131402429 131402429 single base substitution G T upstream_gene_variant PACA-AU 9 131415072 131415072 single base substitution C T intron_variant PACA-AU 9 131421516 131421516 single base substitution C T upstream_gene_variant PACA-AU 9 131422372 131422374 deletion of <=200bp ATT - upstream_gene_variant PACA-CA 9 131392180 131392180 single base substitution G A downstream_gene_variant PACA-CA 9 131392328 131392328 single base substitution C G downstream_gene_variant PACA-CA 9 131392481 131392481 insertion of <=200bp - AAC downstream_gene_variant PACA-CA 9 131392483 131392483 deletion of <=200bp G - downstream_gene_variant PACA-CA 9 131394375 131394375 single base substitution G A downstream_gene_variant PACA-CA 9 131395994 131395994 single base substitution G C 3_prime_UTR_variant PACA-CA 9 131395994 131395994 single base substitution G C downstream_gene_variant PACA-CA 9 131402822 131402822 single base substitution C A intron_variant PACA-CA 9 131402822 131402822 single base substitution C A upstream_gene_variant PACA-CA 9 131405761 131405761 single base substitution G A intron_variant PACA-CA 9 131415398 131415398 single base substitution C A intron_variant PACA-CA 9 131415523 131415523 single base substitution A G intron_variant PACA-CA 9 131419118 131419118 single base substitution C T upstream_gene_variant PACA-CA 9 131419306 131419306 single base substitution C T upstream_gene_variant PACA-CA 9 131420475 131420475 single base substitution C T upstream_gene_variant PACA-CA 9 131420490 131420490 single base substitution G C upstream_gene_variant PACA-CA 9 131422659 131422659 single base substitution G C upstream_gene_variant PACA-CA 9 131423344 131423344 single base substitution G A upstream_gene_variant PACA-CA 9 131423811 131423811 single base substitution C T upstream_gene_variant PAEN-AU 9 131408482 131408482 single base substitution T G intron_variant PAEN-IT 9 131396492 131396492 single base substitution G A downstream_gene_variant PAEN-IT 9 131396492 131396492 single base substitution G A intron_variant PAEN-IT 9 131410489 131410489 single base substitution C A intron_variant PBCA-DE 9 131396915 131396915 single base substitution C T downstream_gene_variant PBCA-DE 9 131396915 131396915 single base substitution C T intron_variant PBCA-DE 9 131412298 131412298 deletion of <=200bp A - intron_variant PBCA-DE 9 131421360 131421360 single base substitution C T upstream_gene_variant PRAD-CA 9 131392570 131392570 single base substitution C A downstream_gene_variant PRAD-CA 9 131397550 131397550 single base substitution G A downstream_gene_variant PRAD-CA 9 131397550 131397550 single base substitution G A intron_variant PRAD-CA 9 131413287 131413287 single base substitution C G intron_variant PRAD-CA 9 131415739 131415739 single base substitution A C intron_variant PRAD-CA 9 131418335 131418335 single base substitution T C intron_variant PRAD-UK 9 131393234 131393234 single base substitution C T downstream_gene_variant PRAD-UK 9 131395932 131395932 single base substitution T C downstream_gene_variant PRAD-UK 9 131411659 131411659 single base substitution G A intron_variant PRAD-UK 9 131418401 131418401 single base substitution G A intron_variant READ-US 9 131418941 131418941 single base substitution G A exon_variant READ-US 9 131418941 131418941 single base substitution G A missense_variant A13V 38C>T READ-US 9 131418941 131418941 single base substitution G A missense_variant A22V 65C>T READ-US 9 131418941 131418941 single base substitution G A missense_variant A7V 20C>T RECA-EU 9 131392510 131392510 single base substitution C A downstream_gene_variant RECA-EU 9 131395756 131395756 single base substitution T C downstream_gene_variant RECA-EU 9 131395759 131395759 single base substitution C A downstream_gene_variant RECA-EU 9 131399345 131399345 single base substitution G A intron_variant RECA-EU 9 131399345 131399345 single base substitution G A upstream_gene_variant RECA-EU 9 131400686 131400686 single base substitution C T intron_variant RECA-EU 9 131400686 131400686 single base substitution C T upstream_gene_variant SKCA-BR 9 131392872 131392872 single base substitution G A downstream_gene_variant SKCA-BR 9 131398473 131398473 single base substitution G C 3_prime_UTR_variant SKCA-BR 9 131398473 131398473 single base substitution G C intron_variant SKCA-BR 9 131398473 131398473 single base substitution G C missense_variant L255V 763C>G SKCA-BR 9 131398473 131398473 single base substitution G C upstream_gene_variant SKCA-BR 9 131399001 131399001 single base substitution A G intron_variant SKCA-BR 9 131399001 131399001 single base substitution A G upstream_gene_variant SKCA-BR 9 131400759 131400759 single base substitution G A intron_variant SKCA-BR 9 131400759 131400759 single base substitution G A upstream_gene_variant SKCA-BR 9 131403861 131403861 single base substitution G A intron_variant SKCA-BR 9 131403861 131403861 single base substitution G A upstream_gene_variant SKCA-BR 9 131404565 131404565 insertion of <=200bp - CA intron_variant SKCA-BR 9 131404732 131404734 deletion of <=200bp CAA - intron_variant SKCA-BR 9 131407467 131407468 deletion of <=200bp TA - intron_variant SKCA-BR 9 131410307 131410307 single base substitution A C intron_variant SKCA-BR 9 131410337 131410337 single base substitution A C intron_variant SKCA-BR 9 131413944 131413944 single base substitution A C intron_variant SKCA-BR 9 131413957 131413957 single base substitution C T intron_variant SKCA-BR 9 131413967 131413967 single base substitution A G intron_variant SKCA-BR 9 131416051 131416051 single base substitution G A intron_variant SKCA-BR 9 131417790 131417791 deletion of <=200bp CA - intron_variant SKCA-BR 9 131418929 131418929 single base substitution A C exon_variant SKCA-BR 9 131418929 131418929 single base substitution A C missense_variant V11G 32T>G SKCA-BR 9 131418929 131418929 single base substitution A C missense_variant V17G 50T>G SKCA-BR 9 131418929 131418929 single base substitution A C missense_variant V26G 77T>G SKCA-BR 9 131421790 131421790 single base substitution A C upstream_gene_variant SKCA-BR 9 131422343 131422343 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 9 131423211 131423211 single base substitution A T upstream_gene_variant SKCM-US 9 131395598 131395598 single base substitution G A downstream_gene_variant SKCM-US 9 131396564 131396564 single base substitution A T downstream_gene_variant SKCM-US 9 131396564 131396564 single base substitution A T missense_variant L438Q 1313T>A SKCM-US 9 131397188 131397188 single base substitution C T downstream_gene_variant SKCM-US 9 131397188 131397188 single base substitution C T exon_variant SKCM-US 9 131397188 131397188 single base substitution C T missense_variant E332K 994G>A SKCM-US 9 131418973 131418973 single base substitution G A synonymous_variant S11S 33C>T SKCM-US 9 131418973 131418973 single base substitution G A synonymous_variant S2S 6C>T SKCM-US 9 131418973 131418973 single base substitution G A upstream_gene_variant STAD-US 9 131392621 131392621 single base substitution G A downstream_gene_variant STAD-US 9 131394978 131394978 single base substitution G A downstream_gene_variant STAD-US 9 131395517 131395517 single base substitution C T downstream_gene_variant STAD-US 9 131395598 131395598 single base substitution G A downstream_gene_variant STAD-US 9 131396155 131396155 single base substitution C T downstream_gene_variant STAD-US 9 131396155 131396155 single base substitution C T synonymous_variant Q493Q 1479G>A STAD-US 9 131396198 131396198 single base substitution G A downstream_gene_variant STAD-US 9 131396198 131396198 single base substitution G A missense_variant T479I 1436C>T STAD-US 9 131396974 131396974 single base substitution A G downstream_gene_variant STAD-US 9 131396974 131396974 single base substitution A G exon_variant STAD-US 9 131396974 131396974 single base substitution A G missense_variant F403S 1208T>C STAD-US 9 131399202 131399202 single base substitution G A exon_variant STAD-US 9 131399202 131399202 single base substitution G A intron_variant STAD-US 9 131399202 131399202 single base substitution G A synonymous_variant Y171Y 513C>T STAD-US 9 131399202 131399202 single base substitution G A synonymous_variant Y180Y 540C>T STAD-US 9 131399202 131399202 single base substitution G A upstream_gene_variant STAD-US 9 131399212 131399212 single base substitution G A exon_variant STAD-US 9 131399212 131399212 single base substitution G A intron_variant STAD-US 9 131399212 131399212 single base substitution G A missense_variant A168V 503C>T STAD-US 9 131399212 131399212 single base substitution G A missense_variant A177V 530C>T STAD-US 9 131399212 131399212 single base substitution G A upstream_gene_variant THCA-SA 9 131396039 131396039 single base substitution G A downstream_gene_variant THCA-SA 9 131396039 131396039 single base substitution G A missense_variant A532V 1595C>T THCA-SA 9 131418828 131418828 single base substitution A C exon_variant THCA-SA 9 131418828 131418828 single base substitution A C missense_variant W45G 133T>G THCA-SA 9 131418828 131418828 single base substitution A C missense_variant W51G 151T>G THCA-SA 9 131418828 131418828 single base substitution A C missense_variant W60G 178T>G THCA-US 9 131397416 131397416 single base substitution G A downstream_gene_variant THCA-US 9 131397416 131397416 single base substitution G A exon_variant THCA-US 9 131397416 131397416 single base substitution G A synonymous_variant F312F 936C>T UCEC-US 9 131394407 131394407 single base substitution G A downstream_gene_variant UCEC-US 9 131394744 131394744 single base substitution G T downstream_gene_variant UCEC-US 9 131394965 131394965 single base substitution C T downstream_gene_variant UCEC-US 9 131394971 131394971 single base substitution A G downstream_gene_variant UCEC-US 9 131395093 131395093 single base substitution C T downstream_gene_variant UCEC-US 9 131395574 131395574 single base substitution C T downstream_gene_variant UCEC-US 9 131395575 131395575 single base substitution G A downstream_gene_variant UCEC-US 9 131396588 131396588 single base substitution G A downstream_gene_variant UCEC-US 9 131396588 131396588 single base substitution G A missense_variant S430L 1289C>T UCEC-US 9 131397170 131397170 insertion of <=200bp - G downstream_gene_variant UCEC-US 9 131397170 131397170 insertion of <=200bp - G exon_variant UCEC-US 9 131397170 131397170 insertion of <=200bp - G frameshift_variant T338T? UCEC-US 9 131398650 131398650 single base substitution G T 3_prime_UTR_variant UCEC-US 9 131398650 131398650 single base substitution G T exon_variant UCEC-US 9 131398650 131398650 single base substitution G T missense_variant L196M 586C>A UCEC-US 9 131398650 131398650 single base substitution G T missense_variant L205M 613C>A UCEC-US 9 131398650 131398650 single base substitution G T upstream_gene_variant UCEC-US 9 131398669 131398669 single base substitution C A 3_prime_UTR_variant UCEC-US 9 131398669 131398669 single base substitution C A exon_variant UCEC-US 9 131398669 131398669 single base substitution C A missense_variant W189C 567G>T UCEC-US 9 131398669 131398669 single base substitution C A missense_variant W198C 594G>T UCEC-US 9 131398669 131398669 single base substitution C A upstream_gene_variant UCEC-US 9 131403014 131403014 single base substitution C T exon_variant UCEC-US 9 131403014 131403014 single base substitution C T missense_variant A116T 346G>A UCEC-US 9 131403014 131403014 single base substitution C T missense_variant A122T 364G>A UCEC-US 9 131403014 131403014 single base substitution C T missense_variant A131T 391G>A UCEC-US 9 131403014 131403014 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-5V8LT COSM403128 c.1520T>C p.V507A Substitution - Missense 9:128633835-128633835 - PTC_407 COSM1580233 c.178T>G p.W60G Substitution - Missense 9:128656549-128656549 - TCGA-BR-6452-01 COSM3904531 c.530C>T p.A177V Substitution - Missense 9:128636933-128636933 - H1703 COSM1196541 c.904G>A p.G302R Substitution - Missense 9:128635169-128635169 - TCGA-AP-A059-01 COSM1105687 c.594G>T p.W198C Substitution - Missense 9:128636390-128636390 - TCGA-CU-A3YL-01 COSM3779712 c.1230C>T p.S410S Substitution - coding silent 9:128634368-128634368 - TCGA-EE-A2GI-06 COSM3654703 c.1313T>A p.L438Q Substitution - Missense 9:128634285-128634285 - SE21PT COSM1580233 c.178T>G p.W60G Substitution - Missense 9:128656549-128656549 - Pat_74_A COSM5875625 c.298C>T p.P100S Substitution - Missense 9:128640828-128640828 - TCGA-DK-A2I4-01 COSM3779711 c.1425G>C p.L475F Substitution - Missense 9:128633930-128633930 - TCGA-AZ-6601-01 COSM3699446 c.542G>A p.G181D Substitution - Missense 9:128636921-128636921 - S02139 COSM5674657 c.198G>T p.Q66H Substitution - Missense 9:128640928-128640928 - TCGA-CG-5728-01 COSM3904529 c.540C>T p.Y180Y Substitution - coding silent 9:128636923-128636923 - TCGA-AH-6544-01 COSM3432892 c.65C>T p.A22V Substitution - Missense 9:128656662-128656662 - TCGA-BR-4363-01 COSM3904528 c.1208T>C p.F403S Substitution - Missense 9:128634695-128634695 - TCGA-AP-A056-01 COSM1105684 c.1289C>T p.S430L Substitution - Missense 9:128634309-128634309 - UM-SCC-4 COSM4599880 c.332T>A p.F111Y Substitution - Missense 9:128640794-128640794 - TCGA-E9-A1RB-01 COSM3847774 c.886C>T p.L296L Substitution - coding silent 9:128635187-128635187 - Pat_74_B COSM5875625 c.298C>T p.P100S Substitution - Missense 9:128640828-128640828 - 587228 COSM1232575 c.605G>A p.R202Q Substitution - Missense 9:128636379-128636379 - TCGA-BR-4201-01 COSM3904526 c.1479G>A p.Q493Q Substitution - coding silent 9:128633876-128633876 - C086 COSM5541709 c.792C>T p.T264T Substitution - coding silent 9:128635679-128635679 - TCGA-CG-4438-01 COSM3904527 c.1436C>T p.T479I Substitution - Missense 9:128633919-128633919 - CHC1079T COSM4791063 c.1055T>C p.L352P Substitution - Missense 9:128634848-128634848 - 2492730 COSM5729132 c.1513G>A p.G505S Substitution - Missense 9:128633842-128633842 - TCGA-66-2783-01 COSM752608 c.1487A>G p.Q496R Substitution - Missense 9:128633868-128633868 - TCGA-EE-A2GJ-06 COSM3654705 c.33C>T p.S11S Substitution - coding silent 9:128656694-128656694 - TCGA-AN-A046-01 COSM3847775 c.310G>A p.D104N Substitution - Missense 9:128640816-128640816 - H1155 COSM1195223 c.1366G>A p.G456R Substitution - Missense 9:128634232-128634232 - TCGA-BT-A42C-01 COSM4390144 c.1026C>T p.F342F Substitution - coding silent 9:128634877-128634877 - TCGA-AP-A059-01 COSM1105686 c.613C>A p.L205M Substitution - Missense 9:128636371-128636371 - 9583_PT COSM5757320 c.1283T>C p.L428S Substitution - Missense 9:128634315-128634315 - C91 COSM4445187 c.937G>A p.A313T Substitution - Missense 9:128635136-128635136 - QGP1 COSM3327529 c.277G>A p.V93M Substitution - Missense 9:128640849-128640849 - SW48 COSM4616036 c.1171_1172insC p.H391fs*24 Insertion - Frameshift 9:128634731-128634732 - T1154 COSM3327532 c.201G>A p.T67T Substitution - coding silent 9:128640925-128640925 - TCGA-A6-5665-01 COSM1460295 c.1068C>T p.G356G Substitution - coding silent 9:128634835-128634835 - SJBALL020625_D1 COSM4993812 c.267G>C p.T89T Substitution - coding silent 9:128640859-128640859 - CSCC-32-T COSM4508632 c.782C>G p.T261R Substitution - Missense 9:128635689-128635689 - TCGA-CK-5916-01 COSM1460295 c.1068C>T p.G356G Substitution - coding silent 9:128634835-128634835 - 9583_CLM COSM5757320 c.1283T>C p.L428S Substitution - Missense 9:128634315-128634315 - TCGA-EE-A2MT-06 COSM3654704 c.994G>A p.E332K Substitution - Missense 9:128634909-128634909 - TCGA-CK-4950-01 COSM455423 c.627G>A p.Q209Q Substitution - coding silent 9:128636357-128636357 - sysucc-1370T COSM5472671 c.1242C>T p.D414D Substitution - coding silent 9:128634356-128634356 - B15 COSM253887 c.1521G>T p.V507V Substitution - coding silent 9:128633834-128633834 - BD57T COSM5510382 c.630G>A p.P210P Substitution - coding silent 9:128636354-128636354 - pfg008T COSM1643751 c.1272G>T p.Q424H Substitution - Missense 9:128634326-128634326 - CHC2216T COSM4806012 c.977A>G p.K326R Substitution - Missense 9:128635096-128635096 - TCGA-ET-A2MY-01 COSM3375112 c.936C>T p.F312F Substitution - coding silent 9:128635137-128635137 - PD9573a COSM5796365 c.200C>T p.T67M Substitution - Missense 9:128640926-128640926 - C80 COSM4619919 c.671C>G p.A224G Substitution - Missense 9:128636313-128636313 - DN110CD COSM5779880 c.877G>A p.G293R Substitution - Missense 9:128635196-128635196 - ZZUFHECRKL-G060T COSM4007061 c.873C>T p.T291T Substitution - coding silent 9:128635200-128635200 - 447 COSM4435178 c.1108_1109insG p.A370fs*45 Insertion - Frameshift 9:128634794-128634795 - BD10T COSM5514530 c.1417A>C p.T473P Substitution - Missense 9:128633938-128633938 - 12-P279 COSM3327525 c.390C>T p.H130H Substitution - coding silent 9:128640736-128640736 - TCGA-AA-3663-01 COSM1460296 c.921G>A p.Q307Q Substitution - coding silent 9:128635152-128635152 - CHC1079T COSM4791063 c.1055T>C p.L352P Substitution - Missense 9:128634848-128634848 - Br27P COSM40762 c.475G>A p.A159T Substitution - Missense 9:128636988-128636988 - TCGA-66-2767-01 COSM752607 c.1339C>T p.R447W Substitution - Missense 9:128634259-128634259 - TCGA-AP-A0LM-01 COSM1105690 c.391G>A p.A131T Substitution - Missense 9:128640735-128640735 - HCC123T COSM5816897 c.1492T>G p.L498V Substitution - Missense 9:128633863-128633863 - TCGA-GV-A3JW-01 COSM1314527 c.762G>T p.L254L Substitution - coding silent 9:128635709-128635709 - PD13162a COSM5779880 c.877G>A p.G293R Substitution - Missense 9:128635196-128635196 - CHC2216T COSM4806012 c.977A>G p.K326R Substitution - Missense 9:128635096-128635096 - HCC043T COSM5811990 c.997A>G p.T333A Substitution - Missense 9:128634906-128634906 - TCGA-G4-6628-01 COSM1460294 c.1324C>T p.R442C Substitution - Missense 9:128634274-128634274 - TCGA-AZ-4615-01 COSM455423 c.627G>A p.Q209Q Substitution - coding silent 9:128636357-128636357 - TCGA-AP-A0LH-01 COSM1105685 c.1011_1012insC p.T338fs*9 Insertion - Frameshift 9:128634891-128634892 - PTC-7C COSM455423 c.627G>A p.Q209Q Substitution - coding silent 9:128636357-128636357 - B80-13-Tumor COSM4007061 c.873C>T p.T291T Substitution - coding silent 9:128635200-128635200 - Br27P COSM40761 c.1484C>T p.T495I Substitution - Missense 9:128633871-128633871 - LIM1899 COSM4640893 c.476C>T p.A159V Substitution - Missense 9:128636987-128636987 - KM12 COSM3327496 c.1512G>A p.Q504Q Substitution - coding silent 9:128633843-128633843 - PTC_435 COSM5957064 c.1595C>T p.A532V Substitution - Missense 9:128633760-128633760 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.495240 9q34.11 613363 2415384|CGAP|BC001614|C/T|coding|Thr174Thr|831|Validated; 2415384|CGAP|BC011874|C/T|coding|Thr174Thr|933|Validated; 2415390|CGAP|BC001614|A/G|coding|Gln92Gln|585|Validated; 2415390|CGAP|BC011874|A/G|coding|Gln92Gln|687|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.F403S c.1208T>C 9 131396974 STAD A - IntronicDeletion . c.814-89delT 9 131397627 STAD A T Missense p.L438Q c.1313T>A 9 131396564 CM C A Missense p.G331W c.991G>T 9 131397191 CM C A Missense p.Q424H c.1272G>T 9 131396605 STAD C A Synonymous p.L254L c.762G>T 9 131397988 BLCA C A Synonymous p.T354T c.1062G>T 9 131397120 STAD C G Missense p.L475F c.1425G>C 9 131396209 BLCA C T Missense p.E332K c.994G>A 9 131397188 CM C T Missense p.T495I c.1484C>T 9 131396150 GBM C T Nonsense p.W245* c.734G>A 9 131398016 CM C T Synonymous p.Q493Q c.1479G>A 9 131396155 STAD C T Synonymous p.S211S c.633G>A 9 131398630 LUAD G A Missense p.A159T c.475G>A 9 131399267 GBM G A Missense p.R283C c.847C>T 9 131397505 HNSC G A Missense p.R447W c.1339C>T 9 131396538 LUSC G A Missense p.R522W c.1564C>T 9 131396070 LUAD G A Missense p.T479I c.1436C>T 9 131396198 STAD G A Synonymous p.F312F c.936C>T 9 131397416 THCA G A Synonymous p.S11S c.33C>T 9 131418973 CM G A Synonymous p.Y180Y c.540C>T 9 131399202 STAD - G Frameshift p.T338Hfs*9 c.1011dupC 9 131397171 UCEC G T Missense p.A532E c.1595C>A 9 131396039 HNSC T C Missense p.H226R c.677A>G 9 131398586 BRCA T C Missense p.Q496R c.1487A>G 9 131396147 LUSC