Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 17 6927018 6927018 + Missense_Mutation SNP G G C TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr17:6927018G>C c.28G>C c.(28-30)Gcg>Ccg p.A10P BLCA 17 6927475 6927475 + Missense_Mutation SNP G G A TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr17:6927475G>A c.253G>A c.(253-255)Gaa>Aaa p.E85K BLCA 17 6928501 6928501 + Missense_Mutation SNP C C T TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr17:6928501C>T c.871C>T c.(871-873)Cgg>Tgg p.R291W BLCA 17 6930283 6930283 + Silent SNP G G C TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr17:6930283G>C c.1200G>C c.(1198-1200)cgG>cgC p.R400R BRCA 17 6927077 6927077 + Silent SNP C C T TCGA-A7-A4SD-01A-11D-A25Q-09 TCGA-A7-A4SD-11A-43D-A25Q-09 g.chr17:6927077C>T c.87C>T c.(85-87)aaC>aaT p.N29N BRCA 17 6928049 6928050 + Frame_Shift_Del DEL GT GT - TCGA-E9-A22G-01A-11D-A159-09 TCGA-E9-A22G-10A-01D-A159-09 g.chr17:6928049_6928050delGT c.731_732delGT c.(730-732)agtfs p.S244fs BRCA 17 6928491 6928491 + Silent SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr17:6928491A>C c.861A>C c.(859-861)tcA>tcC p.S287S BRCA 17 6929853 6929853 + Missense_Mutation SNP G G T TCGA-A8-A08B-01A-11W-A019-09 TCGA-A8-A08B-10A-01W-A021-09 g.chr17:6929853G>T c.967G>T c.(967-969)Gac>Tac p.D323Y BRCA 17 6930108 6930108 + Missense_Mutation SNP G G T TCGA-GM-A3NW-01A-21D-A228-09 TCGA-GM-A3NW-10A-01D-A22A-09 g.chr17:6930108G>T c.1139G>T c.(1138-1140)gGa>gTa p.G380V CESC 17 6930847 6930847 + Missense_Mutation SNP G G A TCGA-DS-A7WI-01A-12D-A351-09 TCGA-DS-A7WI-10A-01D-A351-09 g.chr17:6930847G>A c.1349G>A c.(1348-1350)cGg>cAg p.R450Q CHOL 17 6928019 6928019 + Missense_Mutation SNP C C G TCGA-W5-AA2R-01A-11D-A417-09 TCGA-W5-AA2R-10A-01D-A41A-09 g.chr17:6928019C>G c.701C>G c.(700-702)tCc>tGc p.S234C CHOL 17 6928019 6928019 + Missense_Mutation SNP C C G TCGA-W5-AA34-01A-11D-A417-09 TCGA-W5-AA34-10A-01D-A41A-09 g.chr17:6928019C>G c.701C>G c.(700-702)tCc>tGc p.S234C COAD 17 6927559 6927559 + Missense_Mutation SNP G G T TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr17:6927559G>T c.337G>T c.(337-339)Gcg>Tcg p.A113S COAD 17 6927746 6927746 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr17:6927746G>A c.428G>A c.(427-429)cGc>cAc p.R143H COAD 17 6928447 6928447 + Missense_Mutation SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr17:6928447A>G c.817A>G c.(817-819)Acc>Gcc p.T273A COAD 17 6928472 6928472 + Missense_Mutation SNP C C A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr17:6928472C>A c.842C>A c.(841-843)gCt>gAt p.A281D COAD 17 6928518 6928518 + Splice_Site SNP G G A TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr17:6928518G>A c.888G>A c.(886-888)ccG>ccA p.P296P COAD 17 6930286 6930286 + Silent SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:6930286G>A c.1203G>A c.(1201-1203)gcG>gcA p.A401A COAD 17 6930396 6930396 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:6930396A>G c.1313A>G c.(1312-1314)aAg>aGg p.K438R COAD 17 6930864 6930864 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:6930864C>T c.1366C>T c.(1366-1368)Cgg>Tgg p.R456W COADREAD 17 6927559 6927559 + Missense_Mutation SNP G G T TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr17:6927559G>T c.337G>T c.(337-339)Gcg>Tcg p.A113S COADREAD 17 6927746 6927746 + Missense_Mutation SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr17:6927746G>A c.428G>A c.(427-429)cGc>cAc p.R143H COADREAD 17 6928447 6928447 + Missense_Mutation SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr17:6928447A>G c.817A>G c.(817-819)Acc>Gcc p.T273A COADREAD 17 6928472 6928472 + Missense_Mutation SNP C C A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr17:6928472C>A c.842C>A c.(841-843)gCt>gAt p.A281D COADREAD 17 6928518 6928518 + Splice_Site SNP G G A TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr17:6928518G>A c.888G>A c.(886-888)ccG>ccA p.P296P COADREAD 17 6930286 6930286 + Silent SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:6930286G>A c.1203G>A c.(1201-1203)gcG>gcA p.A401A COADREAD 17 6930396 6930396 + Missense_Mutation SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:6930396A>G c.1313A>G c.(1312-1314)aAg>aGg p.K438R COADREAD 17 6930824 6930824 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr17:6930824C>T c.1326C>T c.(1324-1326)tgC>tgT p.C442C COADREAD 17 6930864 6930864 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:6930864C>T c.1366C>T c.(1366-1368)Cgg>Tgg p.R456W DLBC 17 6930927 6930927 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr17:6930927G>A c.1429G>A c.(1429-1431)Ggg>Agg p.G477R GBM 17 6929925 6929925 + Missense_Mutation SNP C C T TCGA-12-1597-01B-01D-1495-08 TCGA-12-1597-10A-01D-1495-08 g.chr17:6929925C>T c.1039C>T c.(1039-1041)Cgt>Tgt p.R347C GBMLGG 17 6929875 6929875 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:6929875G>A c.989G>A c.(988-990)tGt>tAt p.C330Y GBMLGG 17 6929925 6929925 + Missense_Mutation SNP C C T TCGA-12-1597-01B-01D-1495-08 TCGA-12-1597-10A-01D-1495-08 g.chr17:6929925C>T c.1039C>T c.(1039-1041)Cgt>Tgt p.R347C HNSC 17 6927486 6927486 + Silent SNP C C G TCGA-F7-7848-01A-11D-2129-08 TCGA-F7-7848-10A-01D-2129-08 g.chr17:6927486C>G c.264C>G c.(262-264)ggC>ggG p.G88G HNSC 17 6927606 6927606 + Missense_Mutation SNP C C A TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr17:6927606C>A c.384C>A c.(382-384)caC>caA p.H128Q HNSC 17 6927875 6927875 + Missense_Mutation SNP G G T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr17:6927875G>T c.557G>T c.(556-558)aGc>aTc p.S186I HNSC 17 6928498 6928498 + Missense_Mutation SNP G G A TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr17:6928498G>A c.868G>A c.(868-870)Gaa>Aaa p.E290K HNSC 17 6930330 6930330 + Missense_Mutation SNP C C A TCGA-CV-5444-01A-02D-1512-08 TCGA-CV-5444-11A-01D-1512-08 g.chr17:6930330C>A c.1247C>A c.(1246-1248)aCc>aAc p.T416N HNSC 17 6930392 6930392 + Missense_Mutation SNP G G C TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chr17:6930392G>C c.1309G>C c.(1309-1311)Gag>Cag p.E437Q KIPAN 17 6928020 6928031 + In_Frame_Del DEL CAGCAGCAGCAG CAGCAGCAGCAG - TCGA-B1-A654-01A-11D-A31X-10 TCGA-B1-A654-10A-01D-A31X-10 g.chr17:6928020_6928031delCAGCAGCAGCAG c.702_713delCAGCAGCAGCAG c.(700-714)tccagcagcagcagc>tcc p.234_238SSSSS>S KIRP 17 6928020 6928031 + In_Frame_Del DEL CAGCAGCAGCAG CAGCAGCAGCAG - TCGA-B1-A654-01A-11D-A31X-10 TCGA-B1-A654-10A-01D-A31X-10 g.chr17:6928020_6928031delCAGCAGCAGCAG c.702_713delCAGCAGCAGCAG c.(700-714)tccagcagcagcagc>tcc p.234_238SSSSS>S LGG 17 6929875 6929875 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:6929875G>A c.989G>A c.(988-990)tGt>tAt p.C330Y LUAD 17 6927438 6927438 + Silent SNP A A G TCGA-97-8174-01A-11D-2284-08 TCGA-97-8174-10A-01D-2284-08 g.chr17:6927438A>G c.216A>G c.(214-216)ggA>ggG p.G72G LUAD 17 6927527 6927527 + Missense_Mutation SNP G G T TCGA-44-A4SU-01A-11D-A24P-08 TCGA-44-A4SU-10A-01D-A24P-08 g.chr17:6927527G>T c.305G>T c.(304-306)cGc>cTc p.R102L LUAD 17 6927597 6927597 + Silent SNP G G A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr17:6927597G>A c.375G>A c.(373-375)caG>caA p.Q125Q LUAD 17 6927841 6927841 + Missense_Mutation SNP C C G TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr17:6927841C>G c.523C>G c.(523-525)Cga>Gga p.R175G LUAD 17 6927925 6927925 + Missense_Mutation SNP A A T TCGA-50-5942-01A-21D-1753-08 TCGA-50-5942-10A-01D-1753-08 g.chr17:6927925A>T c.607A>T c.(607-609)Aac>Tac p.N203Y LUAD 17 6929781 6929781 + Nonsense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr17:6929781G>T c.895G>T c.(895-897)Gaa>Taa p.E299* LUAD 17 6930310 6930310 + Silent SNP G G A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr17:6930310G>A c.1227G>A c.(1225-1227)gaG>gaA p.E409E LUSC 17 6927751 6927751 + Silent SNP C C T TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chr17:6927751C>T c.433C>T c.(433-435)Ctg>Ttg p.L145L PAAD 17 6927434 6927434 + Missense_Mutation SNP C C T TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chr17:6927434C>T c.212C>T c.(211-213)gCg>gTg p.A71V PAAD 17 6927518 6927518 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:6927518C>T c.296C>T c.(295-297)tCg>tTg p.S99L PAAD 17 6927858 6927858 + Frame_Shift_Del DEL C C - TCGA-Q3-A5QY-01A-12D-A32N-08 TCGA-Q3-A5QY-10A-01D-A32N-08 g.chr17:6927858delC c.540delC c.(538-540)ggcfs p.G180fs PRAD 17 6930071 6930071 + Missense_Mutation SNP C C G TCGA-CH-5754-01A-11D-1576-08 TCGA-CH-5754-10A-01D-1576-08 g.chr17:6930071C>G c.1102C>G c.(1102-1104)Cca>Gca p.P368A READ 17 6930824 6930824 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr17:6930824C>T c.1326C>T c.(1324-1326)tgC>tgT p.C442C SARC 17 6928000 6928000 + Missense_Mutation SNP C C A TCGA-PT-A8TR-01A-11D-A37C-09 TCGA-PT-A8TR-10A-01D-A37F-09 g.chr17:6928000C>A c.682C>A c.(682-684)Ccc>Acc p.P228T SARC 17 6930824 6930824 + Silent SNP C C T TCGA-DX-AB32-01A-11D-A417-09 TCGA-DX-AB32-10A-01D-A41A-09 g.chr17:6930824C>T c.1326C>T c.(1324-1326)tgC>tgT p.C442C SKCM 17 6927791 6927791 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr17:6927791C>T c.473C>T c.(472-474)cCa>cTa p.P158L SKCM 17 6927948 6927948 + Silent SNP G G A TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr17:6927948G>A c.630G>A c.(628-630)ggG>ggA p.G210G SKCM 17 6927965 6927965 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:6927965G>A c.647G>A c.(646-648)aGa>aAa p.R216K SKCM 17 6928507 6928507 + Missense_Mutation SNP C C T TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr17:6928507C>T c.877C>T c.(877-879)Cgt>Tgt p.R293C SKCM 17 6928507 6928507 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr17:6928507C>T c.877C>T c.(877-879)Cgt>Tgt p.R293C SKCM 17 6929847 6929847 + Missense_Mutation SNP C C T TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr17:6929847C>T c.961C>T c.(961-963)Cct>Tct p.P321S SKCM 17 6929856 6929856 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr17:6929856G>A c.970G>A c.(970-972)Gaa>Aaa p.E324K SKCM 17 6930093 6930093 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr17:6930093G>A c.1124G>A c.(1123-1125)aGc>aAc p.S375N SKCM 17 6930094 6930094 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr17:6930094C>T c.1125C>T c.(1123-1125)agC>agT p.S375S SKCM 17 6930095 6930095 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr17:6930095C>T c.1126C>T c.(1126-1128)Cgc>Tgc p.R376C SKCM 17 6930106 6930106 + Silent SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr17:6930106G>A c.1137G>A c.(1135-1137)tcG>tcA p.S379S SKCM 17 6930107 6930107 + Missense_Mutation SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr17:6930107G>A c.1138G>A c.(1138-1140)Gga>Aga p.G380R SKCM 17 6930341 6930341 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr17:6930341C>T c.1258C>T c.(1258-1260)Cgc>Tgc p.R420C SKCM 17 6930397 6930397 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:6930397G>A c.1314G>A c.(1312-1314)aaG>aaA p.K438K SKCM 17 6930825 6930825 + Missense_Mutation SNP G G A TCGA-EE-A2GN-06A-11D-A196-08 TCGA-EE-A2GN-10A-01D-A198-08 g.chr17:6930825G>A c.1327G>A c.(1327-1329)Gac>Aac p.D443N SKCM 17 6930932 6930932 + Silent SNP G G A TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr17:6930932G>A c.1434G>A c.(1432-1434)ggG>ggA p.G478G

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 17 6927523 6927523 single base substitution C A intron_variant BLCA-CN 17 6927523 6927523 single base substitution C A missense_variant L101M 301C>A BLCA-CN 17 6927523 6927523 single base substitution C A upstream_gene_variant BLCA-CN 17 6927951 6927951 single base substitution C T downstream_gene_variant BLCA-CN 17 6927951 6927951 single base substitution C T synonymous_variant S211S 633C>T BLCA-CN 17 6927951 6927951 single base substitution C T upstream_gene_variant BLCA-US 17 6927018 6927018 single base substitution G C exon_variant BLCA-US 17 6927018 6927018 single base substitution G C missense_variant A10P 28G>C BLCA-US 17 6927018 6927018 single base substitution G C upstream_gene_variant BLCA-US 17 6928501 6928501 single base substitution C T downstream_gene_variant BLCA-US 17 6928501 6928501 single base substitution C T missense_variant R291W 871C>T BLCA-US 17 6928501 6928501 single base substitution C T upstream_gene_variant BLCA-US 17 6930283 6930283 single base substitution G C downstream_gene_variant BLCA-US 17 6930283 6930283 single base substitution G C exon_variant BLCA-US 17 6930283 6930283 single base substitution G C synonymous_variant R400R 1200G>C BLCA-US 17 6930283 6930283 single base substitution G C synonymous_variant R89R 267G>C BRCA-EU 17 6922434 6922434 single base substitution C T upstream_gene_variant BRCA-EU 17 6923489 6923489 single base substitution G A upstream_gene_variant BRCA-EU 17 6923617 6923617 single base substitution T C upstream_gene_variant BRCA-EU 17 6924111 6924111 single base substitution C T upstream_gene_variant BRCA-EU 17 6930012 6930012 single base substitution C A downstream_gene_variant BRCA-EU 17 6930012 6930012 single base substitution C A intron_variant BRCA-EU 17 6930012 6930012 single base substitution C A upstream_gene_variant BRCA-EU 17 6931759 6931759 single base substitution G T 3_prime_UTR_variant BRCA-EU 17 6931759 6931759 single base substitution G T downstream_gene_variant BRCA-EU 17 6931759 6931759 single base substitution G T intron_variant BRCA-EU 17 6932270 6932274 deletion of <=200bp GTAAC - 3_prime_UTR_variant BRCA-EU 17 6932270 6932274 deletion of <=200bp GTAAC - downstream_gene_variant BRCA-EU 17 6932270 6932274 deletion of <=200bp GTAAC - intron_variant BRCA-EU 17 6934386 6934386 single base substitution C G downstream_gene_variant BRCA-EU 17 6935691 6935691 single base substitution G C downstream_gene_variant BRCA-EU 17 6937538 6937538 insertion of <=200bp - C downstream_gene_variant BRCA-FR 17 6923489 6923489 single base substitution G A upstream_gene_variant BRCA-FR 17 6931759 6931759 single base substitution G T 3_prime_UTR_variant BRCA-FR 17 6931759 6931759 single base substitution G T downstream_gene_variant BRCA-FR 17 6931759 6931759 single base substitution G T intron_variant BRCA-FR 17 6934386 6934386 single base substitution C G downstream_gene_variant BRCA-FR 17 6935691 6935691 single base substitution G C downstream_gene_variant BRCA-UK 17 6926503 6926503 single base substitution G C intron_variant BRCA-UK 17 6926503 6926503 single base substitution G C upstream_gene_variant BRCA-US 17 6927077 6927077 single base substitution C T exon_variant BRCA-US 17 6927077 6927077 single base substitution C T synonymous_variant N29N 87C>T BRCA-US 17 6927077 6927077 single base substitution C T upstream_gene_variant BRCA-US 17 6928049 6928050 deletion of <=200bp GT - downstream_gene_variant BRCA-US 17 6928049 6928050 deletion of <=200bp GT - frameshift_variant S244 BRCA-US 17 6928049 6928050 deletion of <=200bp GT - upstream_gene_variant BRCA-US 17 6928491 6928491 single base substitution A C downstream_gene_variant BRCA-US 17 6928491 6928491 single base substitution A C synonymous_variant S287S 861A>C BRCA-US 17 6928491 6928491 single base substitution A C upstream_gene_variant BRCA-US 17 6929853 6929853 single base substitution G T downstream_gene_variant BRCA-US 17 6929853 6929853 single base substitution G T missense_variant D12Y 34G>T BRCA-US 17 6929853 6929853 single base substitution G T missense_variant D323Y 967G>T BRCA-US 17 6929853 6929853 single base substitution G T upstream_gene_variant BRCA-US 17 6930108 6930108 single base substitution G T downstream_gene_variant BRCA-US 17 6930108 6930108 single base substitution G T missense_variant G380V 1139G>T BRCA-US 17 6930108 6930108 single base substitution G T missense_variant G69V 206G>T BRCA-US 17 6930108 6930108 single base substitution G T upstream_gene_variant BTCA-JP 17 6927188 6927188 single base substitution G C intron_variant BTCA-JP 17 6927188 6927188 single base substitution G C upstream_gene_variant CESC-US 17 6930847 6930847 single base substitution G A downstream_gene_variant CESC-US 17 6930847 6930847 single base substitution G A intron_variant CESC-US 17 6930847 6930847 single base substitution G A missense_variant R450Q 1349G>A COAD-US 17 6927559 6927559 single base substitution G T downstream_gene_variant COAD-US 17 6927559 6927559 single base substitution G T exon_variant COAD-US 17 6927559 6927559 single base substitution G T missense_variant A113S 337G>T COAD-US 17 6927559 6927559 single base substitution G T upstream_gene_variant COAD-US 17 6927746 6927746 single base substitution G A downstream_gene_variant COAD-US 17 6927746 6927746 single base substitution G A exon_variant COAD-US 17 6927746 6927746 single base substitution G A missense_variant R143H 428G>A COAD-US 17 6927746 6927746 single base substitution G A upstream_gene_variant COAD-US 17 6928518 6928518 single base substitution G A downstream_gene_variant COAD-US 17 6928518 6928518 single base substitution G A splice_region_variant COAD-US 17 6928518 6928518 single base substitution G A upstream_gene_variant COAD-US 17 6930286 6930286 single base substitution G A downstream_gene_variant COAD-US 17 6930286 6930286 single base substitution G A exon_variant COAD-US 17 6930286 6930286 single base substitution G A synonymous_variant A401A 1203G>A COAD-US 17 6930286 6930286 single base substitution G A synonymous_variant A90A 270G>A COAD-US 17 6930301 6930301 single base substitution C T downstream_gene_variant COAD-US 17 6930301 6930301 single base substitution C T exon_variant COAD-US 17 6930301 6930301 single base substitution C T synonymous_variant H406H 1218C>T COAD-US 17 6930301 6930301 single base substitution C T synonymous_variant H95H 285C>T COAD-US 17 6930864 6930864 single base substitution C T downstream_gene_variant COAD-US 17 6930864 6930864 single base substitution C T intron_variant COAD-US 17 6930864 6930864 single base substitution C T missense_variant R456W 1366C>T COCA-CN 17 6927520 6927520 single base substitution C T intron_variant COCA-CN 17 6927520 6927520 single base substitution C T missense_variant R100C 298C>T COCA-CN 17 6927520 6927520 single base substitution C T upstream_gene_variant COCA-CN 17 6928104 6928104 single base substitution G T downstream_gene_variant COCA-CN 17 6928104 6928104 single base substitution G T intron_variant COCA-CN 17 6928104 6928104 single base substitution G T upstream_gene_variant COCA-CN 17 6928363 6928363 single base substitution C A downstream_gene_variant COCA-CN 17 6928363 6928363 single base substitution C A intron_variant COCA-CN 17 6928363 6928363 single base substitution C A upstream_gene_variant COCA-CN 17 6928501 6928501 single base substitution C T downstream_gene_variant COCA-CN 17 6928501 6928501 single base substitution C T missense_variant R291W 871C>T COCA-CN 17 6928501 6928501 single base substitution C T upstream_gene_variant COCA-CN 17 6933237 6933237 single base substitution C A 3_prime_UTR_variant COCA-CN 17 6933237 6933237 single base substitution C A downstream_gene_variant COCA-CN 17 6933237 6933237 single base substitution C A exon_variant ESAD-UK 17 6923229 6923229 insertion of <=200bp - C upstream_gene_variant ESAD-UK 17 6927520 6927520 single base substitution C T intron_variant ESAD-UK 17 6927520 6927520 single base substitution C T missense_variant R100C 298C>T ESAD-UK 17 6927520 6927520 single base substitution C T upstream_gene_variant ESAD-UK 17 6933519 6933519 single base substitution C A 3_prime_UTR_variant ESAD-UK 17 6933519 6933519 single base substitution C A downstream_gene_variant ESAD-UK 17 6937294 6937294 single base substitution C A downstream_gene_variant ESAD-UK 17 6937322 6937322 insertion of <=200bp - C downstream_gene_variant ESAD-UK 17 6937536 6937536 single base substitution A C downstream_gene_variant ESAD-UK 17 6937657 6937657 single base substitution C T downstream_gene_variant ESAD-UK 17 6938277 6938277 single base substitution G T downstream_gene_variant ESCA-CN 17 6928502 6928502 single base substitution G A downstream_gene_variant ESCA-CN 17 6928502 6928502 single base substitution G A missense_variant R291Q 872G>A ESCA-CN 17 6928502 6928502 single base substitution G A upstream_gene_variant GBM-US 17 6929925 6929925 single base substitution C T downstream_gene_variant GBM-US 17 6929925 6929925 single base substitution C T missense_variant R347C 1039C>T GBM-US 17 6929925 6929925 single base substitution C T missense_variant R36C 106C>T GBM-US 17 6929925 6929925 single base substitution C T upstream_gene_variant KIRP-US 17 6927003 6927003 single base substitution G T exon_variant KIRP-US 17 6927003 6927003 single base substitution G T missense_variant A5S 13G>T KIRP-US 17 6927003 6927003 single base substitution G T upstream_gene_variant LAML-KR 17 6928608 6928608 single base substitution G C downstream_gene_variant LAML-KR 17 6928608 6928608 single base substitution G C intron_variant LAML-KR 17 6928608 6928608 single base substitution G C upstream_gene_variant LAML-KR 17 6930139 6930139 single base substitution C T downstream_gene_variant LAML-KR 17 6930139 6930139 single base substitution C T exon_variant LAML-KR 17 6930139 6930139 single base substitution C T synonymous_variant G390G 1170C>T LAML-KR 17 6930139 6930139 single base substitution C T synonymous_variant G79G 237C>T LICA-CN 17 6928463 6928463 single base substitution C T downstream_gene_variant LICA-CN 17 6928463 6928463 single base substitution C T missense_variant T278I 833C>T LICA-CN 17 6928463 6928463 single base substitution C T upstream_gene_variant LICA-FR 17 6929909 6929909 single base substitution C T downstream_gene_variant LICA-FR 17 6929909 6929909 single base substitution C T synonymous_variant G30G 90C>T LICA-FR 17 6929909 6929909 single base substitution C T synonymous_variant G341G 1023C>T LICA-FR 17 6929909 6929909 single base substitution C T upstream_gene_variant LICA-FR 17 6935478 6935481 deletion of <=200bp ACAC - downstream_gene_variant LIHC-US 17 6927950 6927950 single base substitution G T downstream_gene_variant LIHC-US 17 6927950 6927950 single base substitution G T missense_variant S211I 632G>T LIHC-US 17 6927950 6927950 single base substitution G T upstream_gene_variant LINC-JP 17 6922640 6922640 single base substitution T C upstream_gene_variant LINC-JP 17 6926244 6926244 single base substitution C T upstream_gene_variant LINC-JP 17 6927641 6927641 single base substitution G A downstream_gene_variant LINC-JP 17 6927641 6927641 single base substitution G A intron_variant LINC-JP 17 6927641 6927641 single base substitution G A upstream_gene_variant LIRI-JP 17 6928020 6928020 insertion of <=200bp - CAG downstream_gene_variant LIRI-JP 17 6928020 6928020 insertion of <=200bp - CAG inframe_insertion S234SS LIRI-JP 17 6928020 6928020 insertion of <=200bp - CAG upstream_gene_variant LIRI-JP 17 6932306 6932306 single base substitution G A 3_prime_UTR_variant LIRI-JP 17 6932306 6932306 single base substitution G A downstream_gene_variant LIRI-JP 17 6932306 6932306 single base substitution G A intron_variant LIRI-JP 17 6934939 6934939 single base substitution A C downstream_gene_variant LIRI-JP 17 6936404 6936404 single base substitution G A downstream_gene_variant LIRI-JP 17 6936595 6936595 single base substitution C T downstream_gene_variant LIRI-JP 17 6938514 6938514 single base substitution G T downstream_gene_variant LUSC-KR 17 6931808 6931808 single base substitution G C 3_prime_UTR_variant LUSC-KR 17 6931808 6931808 single base substitution G C downstream_gene_variant LUSC-KR 17 6931808 6931808 single base substitution G C intron_variant LUSC-US 17 6927751 6927751 single base substitution C T downstream_gene_variant LUSC-US 17 6927751 6927751 single base substitution C T exon_variant LUSC-US 17 6927751 6927751 single base substitution C T synonymous_variant L145L 433C>T LUSC-US 17 6927751 6927751 single base substitution C T upstream_gene_variant MALY-DE 17 6927291 6927291 single base substitution G A intron_variant MALY-DE 17 6927291 6927291 single base substitution G A upstream_gene_variant MALY-DE 17 6933981 6933981 single base substitution C T downstream_gene_variant MALY-DE 17 6938310 6938310 single base substitution A C downstream_gene_variant MELA-AU 17 6921349 6921349 single base substitution G A upstream_gene_variant MELA-AU 17 6922857 6922857 single base substitution G A upstream_gene_variant MELA-AU 17 6922891 6922891 single base substitution C T upstream_gene_variant MELA-AU 17 6923118 6923118 single base substitution C G upstream_gene_variant MELA-AU 17 6923364 6923364 single base substitution C T upstream_gene_variant MELA-AU 17 6923485 6923485 single base substitution G A upstream_gene_variant MELA-AU 17 6923784 6923784 single base substitution C T upstream_gene_variant MELA-AU 17 6924131 6924131 single base substitution C T upstream_gene_variant MELA-AU 17 6924657 6924657 single base substitution T C upstream_gene_variant MELA-AU 17 6925468 6925468 single base substitution C T upstream_gene_variant MELA-AU 17 6925748 6925748 single base substitution G A upstream_gene_variant MELA-AU 17 6925988 6925988 single base substitution G A upstream_gene_variant MELA-AU 17 6926005 6926005 single base substitution T C upstream_gene_variant MELA-AU 17 6926206 6926207 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 6926284 6926284 single base substitution G A upstream_gene_variant MELA-AU 17 6926364 6926364 single base substitution G A 5_prime_UTR_variant MELA-AU 17 6926364 6926364 single base substitution G A upstream_gene_variant MELA-AU 17 6926382 6926383 multiple base substitution (>=2bp and <=200bp) CC TT 5_prime_UTR_variant MELA-AU 17 6926382 6926383 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 6926519 6926519 single base substitution G A intron_variant MELA-AU 17 6926519 6926519 single base substitution G A upstream_gene_variant MELA-AU 17 6926841 6926852 deletion of <=200bp TAGGAGGGAGGC - 5_prime_UTR_variant MELA-AU 17 6926841 6926852 deletion of <=200bp TAGGAGGGAGGC - intron_variant MELA-AU 17 6926841 6926852 deletion of <=200bp TAGGAGGGAGGC - upstream_gene_variant MELA-AU 17 6927356 6927356 single base substitution C T intron_variant MELA-AU 17 6927356 6927356 single base substitution C T upstream_gene_variant MELA-AU 17 6927686 6927686 single base substitution G A downstream_gene_variant MELA-AU 17 6927686 6927686 single base substitution G A intron_variant MELA-AU 17 6927686 6927686 single base substitution G A upstream_gene_variant MELA-AU 17 6928148 6928148 single base substitution C T downstream_gene_variant MELA-AU 17 6928148 6928148 single base substitution C T intron_variant MELA-AU 17 6928148 6928148 single base substitution C T upstream_gene_variant MELA-AU 17 6928342 6928342 single base substitution C T downstream_gene_variant MELA-AU 17 6928342 6928342 single base substitution C T intron_variant MELA-AU 17 6928342 6928342 single base substitution C T upstream_gene_variant MELA-AU 17 6928365 6928365 single base substitution C T downstream_gene_variant MELA-AU 17 6928365 6928365 single base substitution C T intron_variant MELA-AU 17 6928365 6928365 single base substitution C T upstream_gene_variant MELA-AU 17 6928458 6928458 single base substitution C T downstream_gene_variant MELA-AU 17 6928458 6928458 single base substitution C T synonymous_variant L276L 828C>T MELA-AU 17 6928458 6928458 single base substitution C T upstream_gene_variant MELA-AU 17 6928487 6928487 single base substitution G A downstream_gene_variant MELA-AU 17 6928487 6928487 single base substitution G A missense_variant G286E 857G>A MELA-AU 17 6928487 6928487 single base substitution G A upstream_gene_variant MELA-AU 17 6928680 6928681 multiple base substitution (>=2bp and <=200bp) TA AT downstream_gene_variant MELA-AU 17 6928680 6928681 multiple base substitution (>=2bp and <=200bp) TA AT intron_variant MELA-AU 17 6928680 6928681 multiple base substitution (>=2bp and <=200bp) TA AT upstream_gene_variant MELA-AU 17 6929466 6929466 single base substitution C T downstream_gene_variant MELA-AU 17 6929466 6929466 single base substitution C T intron_variant MELA-AU 17 6929466 6929466 single base substitution C T upstream_gene_variant MELA-AU 17 6930028 6930028 single base substitution A G downstream_gene_variant MELA-AU 17 6930028 6930028 single base substitution A G synonymous_variant E353E 1059A>G MELA-AU 17 6930028 6930028 single base substitution A G synonymous_variant E42E 126A>G MELA-AU 17 6930028 6930028 single base substitution A G upstream_gene_variant MELA-AU 17 6930053 6930053 single base substitution G A downstream_gene_variant MELA-AU 17 6930053 6930053 single base substitution G A missense_variant G362R 1084G>A MELA-AU 17 6930053 6930053 single base substitution G A missense_variant G51R 151G>A MELA-AU 17 6930053 6930053 single base substitution G A upstream_gene_variant MELA-AU 17 6930106 6930107 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 17 6930106 6930107 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SG379SR MELA-AU 17 6930106 6930107 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SG68SR MELA-AU 17 6930106 6930107 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 6930223 6930223 single base substitution G A downstream_gene_variant MELA-AU 17 6930223 6930223 single base substitution G A exon_variant MELA-AU 17 6930223 6930223 single base substitution G A intron_variant MELA-AU 17 6930231 6930231 single base substitution C T downstream_gene_variant MELA-AU 17 6930231 6930231 single base substitution C T exon_variant MELA-AU 17 6930231 6930231 single base substitution C T intron_variant MELA-AU 17 6930377 6930377 single base substitution C T downstream_gene_variant MELA-AU 17 6930377 6930377 single base substitution C T exon_variant MELA-AU 17 6930377 6930377 single base substitution C T missense_variant R121C 361C>T MELA-AU 17 6930377 6930377 single base substitution C T missense_variant R432C 1294C>T MELA-AU 17 6931172 6931172 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6931172 6931172 single base substitution G A downstream_gene_variant MELA-AU 17 6931172 6931172 single base substitution G A intron_variant MELA-AU 17 6931188 6931189 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 17 6931188 6931189 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 17 6931188 6931189 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 17 6931224 6931224 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6931224 6931224 single base substitution G A downstream_gene_variant MELA-AU 17 6931224 6931224 single base substitution G A intron_variant MELA-AU 17 6931226 6931226 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6931226 6931226 single base substitution G A downstream_gene_variant MELA-AU 17 6931226 6931226 single base substitution G A intron_variant MELA-AU 17 6931777 6931777 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6931777 6931777 single base substitution G A downstream_gene_variant MELA-AU 17 6931777 6931777 single base substitution G A intron_variant MELA-AU 17 6931794 6931794 single base substitution C T 3_prime_UTR_variant MELA-AU 17 6931794 6931794 single base substitution C T downstream_gene_variant MELA-AU 17 6931794 6931794 single base substitution C T intron_variant MELA-AU 17 6932052 6932052 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6932052 6932052 single base substitution G A downstream_gene_variant MELA-AU 17 6932052 6932052 single base substitution G A intron_variant MELA-AU 17 6933170 6933170 single base substitution C T 3_prime_UTR_variant MELA-AU 17 6933170 6933170 single base substitution C T downstream_gene_variant MELA-AU 17 6933170 6933170 single base substitution C T exon_variant MELA-AU 17 6933358 6933358 single base substitution G A 3_prime_UTR_variant MELA-AU 17 6933358 6933358 single base substitution G A downstream_gene_variant MELA-AU 17 6933540 6933540 single base substitution C T 3_prime_UTR_variant MELA-AU 17 6933540 6933540 single base substitution C T downstream_gene_variant MELA-AU 17 6933849 6933849 single base substitution G A downstream_gene_variant MELA-AU 17 6934043 6934043 single base substitution C T downstream_gene_variant MELA-AU 17 6934260 6934260 single base substitution G A downstream_gene_variant MELA-AU 17 6934643 6934643 single base substitution G A downstream_gene_variant MELA-AU 17 6934793 6934793 single base substitution C T downstream_gene_variant MELA-AU 17 6934812 6934812 single base substitution C T downstream_gene_variant MELA-AU 17 6935036 6935036 single base substitution G A downstream_gene_variant MELA-AU 17 6935308 6935308 single base substitution C T downstream_gene_variant MELA-AU 17 6935336 6935337 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 17 6935646 6935646 single base substitution T C downstream_gene_variant MELA-AU 17 6935813 6935813 single base substitution C T downstream_gene_variant MELA-AU 17 6936857 6936857 single base substitution G A downstream_gene_variant MELA-AU 17 6936920 6936921 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 6937361 6937361 single base substitution G C downstream_gene_variant MELA-AU 17 6937781 6937782 multiple base substitution (>=2bp and <=200bp) AA CT downstream_gene_variant MELA-AU 17 6938480 6938480 single base substitution T C downstream_gene_variant MELA-AU 17 6938532 6938532 single base substitution G A downstream_gene_variant ORCA-IN 17 6927615 6927615 single base substitution C A downstream_gene_variant ORCA-IN 17 6927615 6927615 single base substitution C A exon_variant ORCA-IN 17 6927615 6927615 single base substitution C A synonymous_variant I131I 393C>A ORCA-IN 17 6927615 6927615 single base substitution C A upstream_gene_variant ORCA-IN 17 6927858 6927858 single base substitution C A downstream_gene_variant ORCA-IN 17 6927858 6927858 single base substitution C A exon_variant ORCA-IN 17 6927858 6927858 single base substitution C A synonymous_variant G180G 540C>A ORCA-IN 17 6927858 6927858 single base substitution C A upstream_gene_variant ORCA-IN 17 6928050 6928050 single base substitution T C downstream_gene_variant ORCA-IN 17 6928050 6928050 single base substitution T C synonymous_variant S244S 732T>C ORCA-IN 17 6928050 6928050 single base substitution T C upstream_gene_variant ORCA-IN 17 6934857 6934857 single base substitution G A downstream_gene_variant ORCA-IN 17 6935478 6935485 deletion of <=200bp ACACACAC - downstream_gene_variant OV-AU 17 6925768 6925768 single base substitution G A upstream_gene_variant OV-AU 17 6926877 6926877 single base substitution G A 5_prime_UTR_variant OV-AU 17 6926877 6926877 single base substitution G A intron_variant OV-AU 17 6926877 6926877 single base substitution G A upstream_gene_variant OV-AU 17 6927416 6927416 single base substitution C T intron_variant OV-AU 17 6927416 6927416 single base substitution C T missense_variant S65L 194C>T OV-AU 17 6927416 6927416 single base substitution C T upstream_gene_variant OV-AU 17 6927446 6927446 single base substitution T G intron_variant OV-AU 17 6927446 6927446 single base substitution T G missense_variant V75G 224T>G OV-AU 17 6927446 6927446 single base substitution T G upstream_gene_variant OV-AU 17 6929390 6929390 single base substitution G A downstream_gene_variant OV-AU 17 6929390 6929390 single base substitution G A intron_variant OV-AU 17 6929390 6929390 single base substitution G A upstream_gene_variant OV-AU 17 6934891 6934891 single base substitution A C downstream_gene_variant PACA-AU 17 6928918 6928918 single base substitution A C downstream_gene_variant PACA-AU 17 6928918 6928918 single base substitution A C intron_variant PACA-AU 17 6928918 6928918 single base substitution A C upstream_gene_variant PACA-CA 17 6921465 6921465 single base substitution C T upstream_gene_variant PACA-CA 17 6929926 6929926 single base substitution G A downstream_gene_variant PACA-CA 17 6929926 6929926 single base substitution G A missense_variant R347H 1040G>A PACA-CA 17 6929926 6929926 single base substitution G A missense_variant R36H 107G>A PACA-CA 17 6929926 6929926 single base substitution G A upstream_gene_variant PACA-CA 17 6930281 6930281 single base substitution C T downstream_gene_variant PACA-CA 17 6930281 6930281 single base substitution C T exon_variant PACA-CA 17 6930281 6930281 single base substitution C T missense_variant R400W 1198C>T PACA-CA 17 6930281 6930281 single base substitution C T missense_variant R89W 265C>T PACA-CA 17 6935802 6935802 single base substitution C T downstream_gene_variant PACA-CA 17 6935867 6935867 single base substitution G A downstream_gene_variant PAEN-AU 17 6921339 6921339 single base substitution T G upstream_gene_variant PBCA-DE 17 6929018 6929018 single base substitution C T downstream_gene_variant PBCA-DE 17 6929018 6929018 single base substitution C T intron_variant PBCA-DE 17 6929018 6929018 single base substitution C T upstream_gene_variant PBCA-DE 17 6932947 6932947 single base substitution G T 3_prime_UTR_variant PBCA-DE 17 6932947 6932947 single base substitution G T downstream_gene_variant PBCA-DE 17 6932947 6932947 single base substitution G T intron_variant PRAD-CA 17 6926176 6926176 single base substitution G C upstream_gene_variant PRAD-CA 17 6934130 6934130 single base substitution C A downstream_gene_variant PRAD-US 17 6930071 6930071 single base substitution C G downstream_gene_variant PRAD-US 17 6930071 6930071 single base substitution C G missense_variant P368A 1102C>G PRAD-US 17 6930071 6930071 single base substitution C G missense_variant P57A 169C>G PRAD-US 17 6930071 6930071 single base substitution C G upstream_gene_variant READ-US 17 6928507 6928507 single base substitution C T downstream_gene_variant READ-US 17 6928507 6928507 single base substitution C T missense_variant R293C 877C>T READ-US 17 6928507 6928507 single base substitution C T upstream_gene_variant READ-US 17 6930824 6930824 single base substitution C T downstream_gene_variant READ-US 17 6930824 6930824 single base substitution C T intron_variant READ-US 17 6930824 6930824 single base substitution C T splice_region_variant RECA-EU 17 6934135 6934135 single base substitution T G downstream_gene_variant RECA-EU 17 6938192 6938192 single base substitution C A downstream_gene_variant SKCA-BR 17 6921339 6921339 single base substitution T G upstream_gene_variant SKCA-BR 17 6922612 6922612 single base substitution A C upstream_gene_variant SKCA-BR 17 6923071 6923071 single base substitution G A upstream_gene_variant SKCA-BR 17 6923683 6923683 single base substitution C T upstream_gene_variant SKCA-BR 17 6925627 6925627 single base substitution C T upstream_gene_variant SKCA-BR 17 6926997 6926997 single base substitution T C exon_variant SKCA-BR 17 6926997 6926997 single base substitution T C missense_variant S3P 7T>C SKCA-BR 17 6926997 6926997 single base substitution T C upstream_gene_variant SKCA-BR 17 6927707 6927707 single base substitution A C downstream_gene_variant SKCA-BR 17 6927707 6927707 single base substitution A C intron_variant SKCA-BR 17 6927707 6927707 single base substitution A C upstream_gene_variant SKCA-BR 17 6927827 6927827 single base substitution C A downstream_gene_variant SKCA-BR 17 6927827 6927827 single base substitution C A exon_variant SKCA-BR 17 6927827 6927827 single base substitution C A missense_variant P170Q 509C>A SKCA-BR 17 6927827 6927827 single base substitution C A upstream_gene_variant SKCA-BR 17 6928019 6928019 insertion of <=200bp - CCAG downstream_gene_variant SKCA-BR 17 6928019 6928019 insertion of <=200bp - CCAG frameshift_variant S234SS? SKCA-BR 17 6928019 6928019 insertion of <=200bp - CCAG upstream_gene_variant SKCA-BR 17 6930059 6930059 single base substitution C T downstream_gene_variant SKCA-BR 17 6930059 6930059 single base substitution C T missense_variant R364C 1090C>T SKCA-BR 17 6930059 6930059 single base substitution C T missense_variant R53C 157C>T SKCA-BR 17 6930059 6930059 single base substitution C T upstream_gene_variant SKCA-BR 17 6931755 6931755 insertion of <=200bp - CCTGGAGGCTGTGGGTGTGGGGGATTCTGTATCTGGATTCCGTATCACTCCAA 3_prime_UTR_variant SKCA-BR 17 6931755 6931755 insertion of <=200bp - CCTGGAGGCTGTGGGTGTGGGGGATTCTGTATCTGGATTCCGTATCACTCCAA downstream_gene_variant SKCA-BR 17 6931755 6931755 insertion of <=200bp - CCTGGAGGCTGTGGGTGTGGGGGATTCTGTATCTGGATTCCGTATCACTCCAA intron_variant SKCA-BR 17 6931808 6931808 single base substitution G C 3_prime_UTR_variant SKCA-BR 17 6931808 6931808 single base substitution G C downstream_gene_variant SKCA-BR 17 6931808 6931808 single base substitution G C intron_variant SKCA-BR 17 6932820 6932820 single base substitution G A 3_prime_UTR_variant SKCA-BR 17 6932820 6932820 single base substitution G A downstream_gene_variant SKCA-BR 17 6932820 6932820 single base substitution G A intron_variant SKCA-BR 17 6935099 6935099 single base substitution G A downstream_gene_variant SKCA-BR 17 6936162 6936162 insertion of <=200bp - TTTC downstream_gene_variant SKCM-US 17 6927791 6927791 single base substitution C T downstream_gene_variant SKCM-US 17 6927791 6927791 single base substitution C T exon_variant SKCM-US 17 6927791 6927791 single base substitution C T missense_variant P158L 473C>T SKCM-US 17 6927791 6927791 single base substitution C T upstream_gene_variant SKCM-US 17 6927948 6927948 single base substitution G A downstream_gene_variant SKCM-US 17 6927948 6927948 single base substitution G A exon_variant SKCM-US 17 6927948 6927948 single base substitution G A synonymous_variant G210G 630G>A SKCM-US 17 6927948 6927948 single base substitution G A upstream_gene_variant SKCM-US 17 6927965 6927965 single base substitution G A downstream_gene_variant SKCM-US 17 6927965 6927965 single base substitution G A missense_variant R216K 647G>A SKCM-US 17 6927965 6927965 single base substitution G A upstream_gene_variant SKCM-US 17 6928507 6928507 single base substitution C T downstream_gene_variant SKCM-US 17 6928507 6928507 single base substitution C T missense_variant R293C 877C>T SKCM-US 17 6928507 6928507 single base substitution C T upstream_gene_variant SKCM-US 17 6929847 6929847 single base substitution C T downstream_gene_variant SKCM-US 17 6929847 6929847 single base substitution C T missense_variant P10S 28C>T SKCM-US 17 6929847 6929847 single base substitution C T missense_variant P321S 961C>T SKCM-US 17 6929847 6929847 single base substitution C T upstream_gene_variant SKCM-US 17 6929856 6929856 single base substitution G A downstream_gene_variant SKCM-US 17 6929856 6929856 single base substitution G A missense_variant E13K 37G>A SKCM-US 17 6929856 6929856 single base substitution G A missense_variant E324K 970G>A SKCM-US 17 6929856 6929856 single base substitution G A upstream_gene_variant SKCM-US 17 6930093 6930093 single base substitution G A downstream_gene_variant SKCM-US 17 6930093 6930093 single base substitution G A missense_variant S375N 1124G>A SKCM-US 17 6930093 6930093 single base substitution G A missense_variant S64N 191G>A SKCM-US 17 6930093 6930093 single base substitution G A upstream_gene_variant SKCM-US 17 6930341 6930341 single base substitution C T downstream_gene_variant SKCM-US 17 6930341 6930341 single base substitution C T exon_variant SKCM-US 17 6930341 6930341 single base substitution C T missense_variant R109C 325C>T SKCM-US 17 6930341 6930341 single base substitution C T missense_variant R420C 1258C>T SKCM-US 17 6930397 6930397 single base substitution G A downstream_gene_variant SKCM-US 17 6930397 6930397 single base substitution G A exon_variant SKCM-US 17 6930397 6930397 single base substitution G A synonymous_variant K127K 381G>A SKCM-US 17 6930397 6930397 single base substitution G A synonymous_variant K438K 1314G>A SKCM-US 17 6930825 6930825 single base substitution G A downstream_gene_variant SKCM-US 17 6930825 6930825 single base substitution G A intron_variant SKCM-US 17 6930825 6930825 single base substitution G A missense_variant D443N 1327G>A SKCM-US 17 6930932 6930932 single base substitution G A downstream_gene_variant SKCM-US 17 6930932 6930932 single base substitution G A intron_variant SKCM-US 17 6930932 6930932 single base substitution G A synonymous_variant G478G 1434G>A STAD-US 17 6927125 6927125 single base substitution C T exon_variant STAD-US 17 6927125 6927125 single base substitution C T synonymous_variant G45G 135C>T STAD-US 17 6927125 6927125 single base substitution C T upstream_gene_variant STAD-US 17 6927474 6927474 single base substitution C T intron_variant STAD-US 17 6927474 6927474 single base substitution C T synonymous_variant P84P 252C>T STAD-US 17 6927474 6927474 single base substitution C T upstream_gene_variant STAD-US 17 6927479 6927479 single base substitution C T intron_variant STAD-US 17 6927479 6927479 single base substitution C T missense_variant A86V 257C>T STAD-US 17 6927479 6927479 single base substitution C T upstream_gene_variant STAD-US 17 6927489 6927489 single base substitution C T intron_variant STAD-US 17 6927489 6927489 single base substitution C T synonymous_variant F89F 267C>T STAD-US 17 6927489 6927489 single base substitution C T upstream_gene_variant STAD-US 17 6927490 6927490 single base substitution G A intron_variant STAD-US 17 6927490 6927490 single base substitution G A missense_variant A90T 268G>A STAD-US 17 6927490 6927490 single base substitution G A upstream_gene_variant STAD-US 17 6927588 6927588 single base substitution C T downstream_gene_variant STAD-US 17 6927588 6927588 single base substitution C T exon_variant STAD-US 17 6927588 6927588 single base substitution C T synonymous_variant H122H 366C>T STAD-US 17 6927588 6927588 single base substitution C T upstream_gene_variant STAD-US 17 6927806 6927806 single base substitution G A downstream_gene_variant STAD-US 17 6927806 6927806 single base substitution G A exon_variant STAD-US 17 6927806 6927806 single base substitution G A missense_variant R163H 488G>A STAD-US 17 6927806 6927806 single base substitution G A upstream_gene_variant STAD-US 17 6927811 6927811 single base substitution G A downstream_gene_variant STAD-US 17 6927811 6927811 single base substitution G A exon_variant STAD-US 17 6927811 6927811 single base substitution G A missense_variant E165K 493G>A STAD-US 17 6927811 6927811 single base substitution G A upstream_gene_variant STAD-US 17 6927843 6927843 single base substitution A G downstream_gene_variant STAD-US 17 6927843 6927843 single base substitution A G exon_variant STAD-US 17 6927843 6927843 single base substitution A G synonymous_variant R175R 525A>G STAD-US 17 6927843 6927843 single base substitution A G upstream_gene_variant STAD-US 17 6927858 6927858 deletion of <=200bp C - downstream_gene_variant STAD-US 17 6927858 6927858 deletion of <=200bp C - exon_variant STAD-US 17 6927858 6927858 deletion of <=200bp C - frameshift_variant G180 STAD-US 17 6927858 6927858 deletion of <=200bp C - upstream_gene_variant STAD-US 17 6927858 6927858 insertion of <=200bp - C downstream_gene_variant STAD-US 17 6927858 6927858 insertion of <=200bp - C exon_variant STAD-US 17 6927858 6927858 insertion of <=200bp - C frameshift_variant G180G? STAD-US 17 6927858 6927858 insertion of <=200bp - C upstream_gene_variant STAD-US 17 6929846 6929846 single base substitution T C downstream_gene_variant STAD-US 17 6929846 6929846 single base substitution T C synonymous_variant V320V 960T>C STAD-US 17 6929846 6929846 single base substitution T C synonymous_variant V9V 27T>C STAD-US 17 6929846 6929846 single base substitution T C upstream_gene_variant STAD-US 17 6930069 6930069 single base substitution G A downstream_gene_variant STAD-US 17 6930069 6930069 single base substitution G A missense_variant R367Q 1100G>A STAD-US 17 6930069 6930069 single base substitution G A missense_variant R56Q 167G>A STAD-US 17 6930069 6930069 single base substitution G A upstream_gene_variant STAD-US 17 6930312 6930312 single base substitution A C downstream_gene_variant STAD-US 17 6930312 6930312 single base substitution A C exon_variant STAD-US 17 6930312 6930312 single base substitution A C missense_variant K410T 1229A>C STAD-US 17 6930312 6930312 single base substitution A C missense_variant K99T 296A>C STAD-US 17 6930865 6930865 single base substitution G A downstream_gene_variant STAD-US 17 6930865 6930865 single base substitution G A intron_variant STAD-US 17 6930865 6930865 single base substitution G A missense_variant R456Q 1367G>A STAD-US 17 6930927 6930927 deletion of <=200bp G - downstream_gene_variant STAD-US 17 6930927 6930927 deletion of <=200bp G - frameshift_variant G477 STAD-US 17 6930927 6930927 deletion of <=200bp G - intron_variant UCEC-US 17 6927434 6927434 single base substitution C T intron_variant UCEC-US 17 6927434 6927434 single base substitution C T missense_variant A71V 212C>T UCEC-US 17 6927434 6927434 single base substitution C T upstream_gene_variant UCEC-US 17 6927466 6927466 single base substitution G A intron_variant UCEC-US 17 6927466 6927466 single base substitution G A missense_variant G82R 244G>A UCEC-US 17 6927466 6927466 single base substitution G A upstream_gene_variant UCEC-US 17 6927842 6927842 single base substitution G A downstream_gene_variant UCEC-US 17 6927842 6927842 single base substitution G A exon_variant UCEC-US 17 6927842 6927842 single base substitution G A missense_variant R175Q 524G>A UCEC-US 17 6927842 6927842 single base substitution G A upstream_gene_variant UCEC-US 17 6927918 6927918 single base substitution C T downstream_gene_variant UCEC-US 17 6927918 6927918 single base substitution C T exon_variant UCEC-US 17 6927918 6927918 single base substitution C T synonymous_variant I200I 600C>T UCEC-US 17 6927918 6927918 single base substitution C T upstream_gene_variant UCEC-US 17 6928019 6928019 insertion of <=200bp - CAG disruptive_inframe_insertion S234SA UCEC-US 17 6928019 6928019 insertion of <=200bp - CAG downstream_gene_variant UCEC-US 17 6928019 6928019 insertion of <=200bp - CAG upstream_gene_variant UCEC-US 17 6929795 6929795 single base substitution C T downstream_gene_variant UCEC-US 17 6929795 6929795 single base substitution C T synonymous_variant C303C 909C>T UCEC-US 17 6929795 6929795 single base substitution C T upstream_gene_variant UCEC-US 17 6929886 6929886 single base substitution C T downstream_gene_variant UCEC-US 17 6929886 6929886 single base substitution C T missense_variant R23W 67C>T UCEC-US 17 6929886 6929886 single base substitution C T missense_variant R334W 1000C>T UCEC-US 17 6929886 6929886 single base substitution C T upstream_gene_variant UCEC-US 17 6930052 6930052 single base substitution C T downstream_gene_variant UCEC-US 17 6930052 6930052 single base substitution C T synonymous_variant C361C 1083C>T UCEC-US 17 6930052 6930052 single base substitution C T synonymous_variant C50C 150C>T UCEC-US 17 6930052 6930052 single base substitution C T upstream_gene_variant UCEC-US 17 6930059 6930059 single base substitution C T downstream_gene_variant UCEC-US 17 6930059 6930059 single base substitution C T missense_variant R364C 1090C>T UCEC-US 17 6930059 6930059 single base substitution C T missense_variant R53C 157C>T UCEC-US 17 6930059 6930059 single base substitution C T upstream_gene_variant UCEC-US 17 6930334 6930334 single base substitution C T downstream_gene_variant UCEC-US 17 6930334 6930334 single base substitution C T exon_variant UCEC-US 17 6930334 6930334 single base substitution C T synonymous_variant C106C 318C>T UCEC-US 17 6930334 6930334 single base substitution C T synonymous_variant C417C 1251C>T UCEC-US 17 6930373 6930373 single base substitution C T downstream_gene_variant UCEC-US 17 6930373 6930373 single base substitution C T exon_variant UCEC-US 17 6930373 6930373 single base substitution C T synonymous_variant H119H 357C>T UCEC-US 17 6930373 6930373 single base substitution C T synonymous_variant H430H 1290C>T UCEC-US 17 6930407 6930407 single base substitution G A downstream_gene_variant UCEC-US 17 6930407 6930407 single base substitution G A splice_donor_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand WSU-HN6 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + WSU-HN8 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + UM-SCC-2 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + ID01 COSM1166709 c.1013G>A p.R338H Substitution - Missense 17:7026580-7026580 + TCGA-BR-8382-01 COSM4069136 c.1367G>A p.R456Q Substitution - Missense 17:7027546-7027546 + PCSI_0083_Pa_X COSM5420447 c.1198C>T p.R400W Substitution - Missense 17:7026962-7026962 + TCGA-D5-6924-01 COSM1385667 c.888G>A p.P296P Substitution - coding silent 17:7025199-7025199 + TCGA-BS-A0UF-01 COSM983706 c.600C>T p.I200I Substitution - coding silent 17:7024599-7024599 + TCGA-ER-A19H-06 COSM3521510 c.1434G>A p.G478G Substitution - coding silent 17:7027613-7027613 + TCGA-IZ-A6M9-01 COSM3989280 c.13G>T p.A5S Substitution - Missense 17:7023684-7023684 + TCGA-A5-A0GD-01 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + T3092 COSM4665440 c.1221C>T p.T407T Substitution - coding silent 17:7026985-7026985 + WSU-HN8 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-AP-A0LM-01 COSM983699 c.212C>T p.A71V Substitution - Missense 17:7024115-7024115 + TCGA-CD-A4MG-01 COSM4069116 c.257C>T p.A86V Substitution - Missense 17:7024160-7024160 + CAL27 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-BS-A0TG-01 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + D-03 COSM4766380 c.1001G>A p.R334Q Substitution - Missense 17:7026568-7026568 + TCGA-AX-A05Z-01 COSM983705 c.600C>T p.I200I Substitution - coding silent 17:7024599-7024599 + TCGA-HU-A4H4-01 COSM4069133 c.1229A>C p.K410T Substitution - Missense 17:7026993-7026993 + TCGA-BS-A0TG-01 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-EE-A2GN-06 COSM3521508 c.1327G>A p.D443N Substitution - Missense 17:7027506-7027506 + LS411 COSM4614469 c.540delC p.S183fs*20 Deletion - Frameshift 17:7024539-7024539 + S00539 COSM5658764 c.1186-3C>A p.? Unknown 17:7026947-7026947 + Pat_24_A COSM5853353 c.1390G>A p.G464R Substitution - Missense 17:7027569-7027569 + sysucc-1163T COSM5458647 c.298C>T p.R100C Substitution - Missense 17:7024201-7024201 + ESCC_116 COSM5639876 c.632G>A p.S211N Substitution - Missense 17:7024631-7024631 + HCC058T COSM5804418 c.833C>T p.T278I Substitution - Missense 17:7025144-7025144 + TCGA-AY-4071-01 COSM308638 c.539_540insC p.S183fs*6 Insertion - Frameshift 17:7024538-7024539 + UM-SCC-47 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-12-1597-01 COSM2976073 c.1039C>T p.R347C Substitution - Missense 17:7026606-7026606 + TCGA-A5-A0GA-01 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + NOKSI COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + UPCI:SCC090 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + PTC-14C COSM4130540 c.1328A>C p.D443A Substitution - Missense 17:7027507-7027507 + SCC-25 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-CK-5913-01 COSM1385664 c.842C>A p.A281D Substitution - Missense 17:7025153-7025153 + NOKSI COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CHC896T COSM4953603 c.1023C>T p.G341G Substitution - coding silent 17:7026590-7026590 + TCGA-EI-6917-01 COSM3421862 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + TCGA-EI-6507-01 COSM1563667 c.1326C>T p.C442C Substitution - coding silent 17:7027505-7027505 + TCGA-ER-A19H-06 COSM3521509 c.1434G>A p.G478G Substitution - coding silent 17:7027613-7027613 + TCGA-CH-5754-01 COSM1130181 c.1102C>G p.P368A Substitution - Missense 17:7026752-7026752 + CSCC-27-T COSM4499823 c.550C>T p.P184S Substitution - Missense 17:7024549-7024549 + T3446 COSM4665437 c.404A>G p.Y135C Substitution - Missense 17:7024403-7024403 + Z138 COSM1741109 c.726_727insAAG p.S242_S243insK Insertion - In frame 17:7024725-7024726 + TCGA-EE-A2MR-06 COSM3521500 c.647G>A p.R216K Substitution - Missense 17:7024646-7024646 + WSU-HN6 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + PTC-14C COSM4130539 c.1328A>C p.D443A Substitution - Missense 17:7027507-7027507 + TCGA-EE-A3J4-06 COSM3890286 c.630G>A p.G210G Substitution - coding silent 17:7024629-7024629 + TCGA-D1-A174-01 COSM983701 c.244G>A p.G82R Substitution - Missense 17:7024147-7024147 + AOCS-130-1-0 COSM4139779 c.194C>T p.S65L Substitution - Missense 17:7024097-7024097 + TCGA-AP-A0LM-01 COSM983714 c.1083C>T p.C361C Substitution - coding silent 17:7026733-7026733 + TCGA-B5-A0K6-01 COSM983723 c.1379G>A p.R460H Substitution - Missense 17:7027558-7027558 + TCGA-AA-3672-01 COSM266087 c.817A>G p.T273A Substitution - Missense 17:7025128-7025128 + 93VU147T COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-BR-A4QL-01 COSM4069131 c.1100G>A p.R367Q Substitution - Missense 17:7026750-7026750 + UM-SCC-4 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + OSCC-GB_01240111 COSM4270561 c.732T>C p.S244S Substitution - coding silent 17:7024731-7024731 + CHC896T COSM4953603 c.1023C>T p.G341G Substitution - coding silent 17:7026590-7026590 + TCGA-K4-A3WU-01 COSM2976066 c.871C>T p.R291W Substitution - Missense 17:7025182-7025182 + S01512 COSM309453 c.545C>T p.P182L Substitution - Missense 17:7024544-7024544 + C086 COSM3521502 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + CN-AML-08-T COSM5426075 c.1170C>T p.G390G Substitution - coding silent 17:7026820-7026820 + TCGA-A8-A08B-01 COSM437258 c.967G>T p.D323Y Substitution - Missense 17:7026534-7026534 + TCGA-AA-3818-01 COSM308638 c.539_540insC p.S183fs*6 Insertion - Frameshift 17:7024538-7024539 + TCGA-D1-A17Q-01 COSM983703 c.524G>A p.R175Q Substitution - Missense 17:7024523-7024523 + ORL-48 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-HU-A4H4-01 COSM4069134 c.1229A>C p.K410T Substitution - Missense 17:7026993-7026993 + C086 COSM3521501 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + B84-Tumor COSM3932711 c.301C>A p.L101M Substitution - Missense 17:7024204-7024204 + 19M COSM5578110 c.1172C>T p.S391L Substitution - Missense 17:7026822-7026822 + PT46 COSM5929706 c.541C>T p.P181S Substitution - Missense 17:7024540-7024540 + B59-Tumor COSM3932712 c.633C>T p.S211S Substitution - coding silent 17:7024632-7024632 + PCSI_0049_Pa_X COSM3787416 c.1040G>A p.R347H Substitution - Missense 17:7026607-7026607 + TCGA-BR-4362-01 COSM4069111 c.135C>T p.G45G Substitution - coding silent 17:7023806-7023806 + OSCC-GB_00140111 COSM3712431 c.393C>A p.I131I Substitution - coding silent 17:7024296-7024296 + TCGA-BS-A0UF-01 COSM983705 c.600C>T p.I200I Substitution - coding silent 17:7024599-7024599 + TCGA-AP-A0LM-01 COSM983718 c.1251C>T p.C417C Substitution - coding silent 17:7027015-7027015 + S02246 COSM5678909 c.406G>T p.E136* Substitution - Nonsense 17:7024405-7024405 + pfg127T COSM4749385 c.1207G>A p.V403M Substitution - Missense 17:7026971-7026971 + S01512 COSM5668780 c.545C>T p.P182L Substitution - Missense 17:7024544-7024544 + Pat_06_A COSM4614468 c.540delC p.S183fs*20 Deletion - Frameshift 17:7024539-7024539 + TCGA-HU-A4GN-01 COSM4069119 c.268G>A p.A90T Substitution - Missense 17:7024171-7024171 + TCGA-CG-5733-01 COSM4069118 c.267C>T p.F89F Substitution - coding silent 17:7024170-7024170 + PCSI_0083_Pa_X COSM5420446 c.1198C>T p.R400W Substitution - Missense 17:7026962-7026962 + SCC-9 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-HF-7132-01 COSM4069128 c.525A>G p.R175R Substitution - coding silent 17:7024524-7024524 + T469 COSM4665434 c.248G>A p.G83D Substitution - Missense 17:7024151-7024151 + TCGA-FW-A3R5-06 COSM3890289 c.1314G>A p.K438K Substitution - coding silent 17:7027078-7027078 + TCGA-BF-A3DJ-01 COSM3521501 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + TCGA-CG-5733-01 COSM4069117 c.267C>T p.F89F Substitution - coding silent 17:7024170-7024170 + S00539 COSM5658763 c.1186-3C>A p.? Unknown 17:7026947-7026947 + UM-SCC-17B COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + D-03 COSM4766381 c.1001G>A p.R334Q Substitution - Missense 17:7026568-7026568 + TCGA-BR-A4QL-01 COSM4069132 c.1100G>A p.R367Q Substitution - Missense 17:7026750-7026750 + ORL-48 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-FW-A3R5-06 COSM3890290 c.1314G>A p.K438K Substitution - coding silent 17:7027078-7027078 + GHE0776 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-HU-A4GQ-01 COSM4069125 c.493G>A p.E165K Substitution - Missense 17:7024492-7024492 + TCGA-EE-A29E-06 COSM3521503 c.1124G>A p.S375N Substitution - Missense 17:7026774-7026774 + TCGA-E9-A22G-01 COSM5833374 c.731_732delGT p.S244fs*46 Deletion - Frameshift 17:7024730-7024731 + TCGA-A6-A567-01 COSM2976084 c.1149G>A p.P383P Substitution - coding silent 17:7026799-7026799 + TCGA-CD-A4MG-01 COSM4069129 c.960T>C p.V320V Substitution - coding silent 17:7026527-7026527 + SCC-15 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + WSU-HN13 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + PT48 COSM5933527 c.314C>T p.P105L Substitution - Missense 17:7024217-7024217 + UM-SCC-17B COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + GHE0776 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + UM-SCC-11B COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-G4-6320-01 COSM3691758 c.1218C>T p.H406H Substitution - coding silent 17:7026982-7026982 + OSCC-GB_01240111 COSM4270560 c.732T>C p.S244S Substitution - coding silent 17:7024731-7024731 + TCGA-12-1597-01 COSM2976072 c.1039C>T p.R347C Substitution - Missense 17:7026606-7026606 + UPCI:SCC090 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + C058 COSM5524635 c.1007C>T p.S336L Substitution - Missense 17:7026574-7026574 + S02299 COSM5701423 c.454_455insC p.T154fs*7 Insertion - Frameshift 17:7024453-7024454 + TCGA-FD-A3SS-01 COSM3796016 c.28G>C p.A10P Substitution - Missense 17:7023699-7023699 + S01512 COSM309453 c.545C>T p.P182L Substitution - Missense 17:7024544-7024544 + BICR_22 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + HCC2998 COSM1679444 c.115G>A p.D39N Substitution - Missense 17:7023786-7023786 + HCC2998 COSM1679444 c.115G>A p.D39N Substitution - Missense 17:7023786-7023786 + OSCC-GB_00080111 COSM3718510 c.540C>A p.G180G Substitution - coding silent 17:7024539-7024539 + CN-AML-NR-08-Dx COSM5426076 c.1170C>T p.G390G Substitution - coding silent 17:7026820-7026820 + OSCC-GB_00080111 COSM3718511 c.540C>A p.G180G Substitution - coding silent 17:7024539-7024539 + PT49 COSM5524634 c.1007C>T p.S336L Substitution - Missense 17:7026574-7026574 + TCGA-CH-5754-01 COSM1130180 c.1102C>G p.P368A Substitution - Missense 17:7026752-7026752 + TCGA-GM-A3NW-01 COSM3820417 c.1139G>T p.G380V Substitution - Missense 17:7026789-7026789 + TCGA-HF-7132-01 COSM4069127 c.525A>G p.R175R Substitution - coding silent 17:7024524-7024524 + WSU-HN13 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-A2-A0T5-01 COSM3820416 c.861A>C p.S287S Substitution - coding silent 17:7025172-7025172 + ESCC_25 COSM4270563 c.733G>A p.E245K Substitution - Missense 17:7024732-7024732 + TCGA-G3-A25W-01 COSM4927260 c.632G>T p.S211I Substitution - Missense 17:7024631-7024631 + TCGA-AP-A0LM-01 COSM983717 c.1251C>T p.C417C Substitution - coding silent 17:7027015-7027015 + S02273 COSM5681709 c.618C>A p.A206A Substitution - coding silent 17:7024617-7024617 + TCGA-D3-A5GO-06 COSM3521506 c.1258C>T p.R420C Substitution - Missense 17:7027022-7027022 + PT46 COSM5929707 c.541C>T p.P181S Substitution - Missense 17:7024540-7024540 + TCGA-AX-A0J0-01 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + UD-SCC-2 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + SC_9081 COSM4069121 c.366C>T p.H122H Substitution - coding silent 17:7024269-7024269 + TCGA-AX-A05Z-01 COSM983706 c.600C>T p.I200I Substitution - coding silent 17:7024599-7024599 + Pat_24_A COSM5853354 c.1390G>A p.G464R Substitution - Missense 17:7027569-7027569 + HCC2998 COSM1679445 c.115G>A p.D39N Substitution - Missense 17:7023786-7023786 + B59-Tumor COSM3932713 c.633C>T p.S211S Substitution - coding silent 17:7024632-7024632 + TCGA-DA-A1I7-06 COSM3890287 c.961C>T p.P321S Substitution - Missense 17:7026528-7026528 + ESCC_25 COSM4270562 c.733G>A p.E245K Substitution - Missense 17:7024732-7024732 + TCGA-A5-A0GD-01 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + YUKAT COSM5387164 c.1299C>T p.I433I Substitution - coding silent 17:7027063-7027063 + 587284 COSM1184597 c.1105G>T p.A369S Substitution - Missense 17:7026755-7026755 + ESCC_BICR_016T COSM5439527 c.872G>A p.R291Q Substitution - Missense 17:7025183-7025183 + TCGA-AZ-6598-01 COSM1385672 c.1203G>A p.A401A Substitution - coding silent 17:7026967-7026967 + TCGA-BR-4201-01 COSM4069122 c.366C>T p.H122H Substitution - coding silent 17:7024269-7024269 + PT37 COSM5921091 c.1056G>A p.G352G Substitution - coding silent 17:7026706-7026706 + 14T COSM3712430 c.393C>A p.I131I Substitution - coding silent 17:7024296-7024296 + ESCC_116 COSM5639875 c.632G>A p.S211N Substitution - Missense 17:7024631-7024631 + 93VU147T COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CHC896T COSM4953602 c.1023C>T p.G341G Substitution - coding silent 17:7026590-7026590 + LPJ119 COSM1316805 c.887C>A p.P296Q Substitution - Missense 17:7025198-7025198 + SC_9081 COSM4069122 c.366C>T p.H122H Substitution - coding silent 17:7024269-7024269 + PT20_1 COSM5900610 c.890-4C>T p.? Unknown 17:7026453-7026453 + TCGA-AP-A059-01 COSM983710 c.909C>T p.C303C Substitution - coding silent 17:7026476-7026476 + CN-AML-NR-08-Dx COSM5426075 c.1170C>T p.G390G Substitution - coding silent 17:7026820-7026820 + C058 COSM5524634 c.1007C>T p.S336L Substitution - Missense 17:7026574-7026574 + TCGA-B5-A11Y-01 COSM983715 c.1090C>T p.R364C Substitution - Missense 17:7026740-7026740 + HCC058T COSM5804417 c.833C>T p.T278I Substitution - Missense 17:7025144-7025144 + PT37 COSM5921092 c.1056G>A p.G352G Substitution - coding silent 17:7026706-7026706 + S02299 COSM5701424 c.454_455insC p.T154fs*7 Insertion - Frameshift 17:7024453-7024454 + CSCC-7-T COSM4459594 c.1131C>T p.I377I Substitution - coding silent 17:7026781-7026781 + T2269 COSM4665439 c.1074C>T p.C358C Substitution - coding silent 17:7026724-7026724 + TCGA-AA-3971-01 COSM297221 c.807T>C p.A269A Substitution - coding silent 17:7025118-7025118 + YUKAT COSM5387165 c.1299C>T p.I433I Substitution - coding silent 17:7027063-7027063 + TCGA-G3-A25W-01 COSM4927259 c.632G>T p.S211I Substitution - Missense 17:7024631-7024631 + WSU-HN30 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CN-AML-08-T COSM5426076 c.1170C>T p.G390G Substitution - coding silent 17:7026820-7026820 + TCGA-A7-A4SD-01 COSM3820413 c.87C>T p.N29N Substitution - coding silent 17:7023758-7023758 + Detroit_562 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-EE-A2MR-06 COSM3521499 c.647G>A p.R216K Substitution - Missense 17:7024646-7024646 + TCGA-AZ-6598-01 COSM1385673 c.1203G>A p.A401A Substitution - coding silent 17:7026967-7026967 + CAL27 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + PT20_1 COSM5900611 c.890-4C>T p.? Unknown 17:7026453-7026453 + TCGA-D7-6820-01 COSM4069114 c.252C>T p.P84P Substitution - coding silent 17:7024155-7024155 + 6 COSM5732369 c.256G>T p.A86S Substitution - Missense 17:7024159-7024159 + AOCS-086-3-2 COSM4139780 c.224T>G p.V75G Substitution - Missense 17:7024127-7024127 + TCGA-FS-A1ZA-06 COSM3421861 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + TCGA-EE-A2GJ-06 COSM3521502 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + TCGA-AX-A0J1-01 COSM983712 c.1000C>T p.R334W Substitution - Missense 17:7026567-7026567 + T3092 COSM4665441 c.1221C>T p.T407T Substitution - coding silent 17:7026985-7026985 + 6 COSM5732370 c.256G>T p.A86S Substitution - Missense 17:7024159-7024159 + TCGA-AA-3492-01 COSM1385674 c.1313A>G p.K438R Substitution - Missense 17:7027077-7027077 + TCGA-CD-A4MG-01 COSM4069115 c.257C>T p.A86V Substitution - Missense 17:7024160-7024160 + S02246 COSM5678910 c.406G>T p.E136* Substitution - Nonsense 17:7024405-7024405 + sysucc-1163T COSM5458646 c.298C>T p.R100C Substitution - Missense 17:7024201-7024201 + PT49 COSM5524635 c.1007C>T p.S336L Substitution - Missense 17:7026574-7026574 + TCGA-GM-A3NW-01 COSM3820418 c.1139G>T p.G380V Substitution - Missense 17:7026789-7026789 + UM-SCC-4 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + 230 COSM3730398 c.427C>T p.R143C Substitution - Missense 17:7024426-7024426 + TCGA-BG-A0W1-01 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-43-2578-01 COSM707426 c.433C>T p.L145L Substitution - coding silent 17:7024432-7024432 + TCGA-EE-A29E-06 COSM3521504 c.1124G>A p.S375N Substitution - Missense 17:7026774-7026774 + Pat_06_A COSM4614469 c.540delC p.S183fs*20 Deletion - Frameshift 17:7024539-7024539 + TCGA-DM-A1HA-01 COSM1385660 c.337G>T p.A113S Substitution - Missense 17:7024240-7024240 + UM-SCC-11B COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CAL33 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-A2-A0T5-01 COSM3820415 c.861A>C p.S287S Substitution - coding silent 17:7025172-7025172 + TCGA-DM-A1HA-01 COSM1385661 c.337G>T p.A113S Substitution - Missense 17:7024240-7024240 + LPJ119 COSM1316806 c.887C>A p.P296Q Substitution - Missense 17:7025198-7025198 + VCB-PH-10T COSM4770701 c.1168G>T p.G390C Substitution - Missense 17:7026818-7026818 + TCGA-AX-A0J1-01 COSM983711 c.1000C>T p.R334W Substitution - Missense 17:7026567-7026567 + KM12 COSM4612762 c.538_539insC p.G180fs*9 Insertion - Frameshift 17:7024537-7024538 + KM12 COSM4612761 c.538_539insC p.G180fs*9 Insertion - Frameshift 17:7024537-7024538 + 230 COSM3730397 c.427C>T p.R143C Substitution - Missense 17:7024426-7024426 + TCGA-AP-A0LM-01 COSM983713 c.1083C>T p.C361C Substitution - coding silent 17:7026733-7026733 + TCGA-D7-6820-01 COSM4069113 c.252C>T p.P84P Substitution - coding silent 17:7024155-7024155 + S02273 COSM5681708 c.618C>A p.A206A Substitution - coding silent 17:7024617-7024617 + ESCC_BICR_016T COSM5439526 c.872G>A p.R291Q Substitution - Missense 17:7025183-7025183 + TCGA-EE-A2GJ-06 COSM3521501 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + TCGA-HU-A4GQ-01 COSM4069126 c.493G>A p.E165K Substitution - Missense 17:7024492-7024492 + PT48 COSM5933528 c.314C>T p.P105L Substitution - Missense 17:7024217-7024217 + TCGA-AX-A0J0-01 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-EE-A3J4-06 COSM3890285 c.630G>A p.G210G Substitution - coding silent 17:7024629-7024629 + TCGA-D3-A5GO-06 COSM3521505 c.1258C>T p.R420C Substitution - Missense 17:7027022-7027022 + VCB-PH-10T COSM4770702 c.1168G>T p.G390C Substitution - Missense 17:7026818-7026818 + PCSI_0049_Pa_X COSM3787417 c.1040G>A p.R347H Substitution - Missense 17:7026607-7026607 + TCGA-EE-A2GN-06 COSM3521507 c.1327G>A p.D443N Substitution - Missense 17:7027506-7027506 + TCGA-A5-A0GB-01 COSM983721 c.1323+1G>A p.? Unknown 17:7027088-7027088 + BICR_22 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CHC896T COSM4953602 c.1023C>T p.G341G Substitution - coding silent 17:7026590-7026590 + Z138 COSM1741108 c.726_727insAAG p.S242_S243insK Insertion - In frame 17:7024725-7024726 + pfg127T COSM4749386 c.1207G>A p.V403M Substitution - Missense 17:7026971-7026971 + CSCC-29-T COSM4513871 c.953C>T p.S318F Substitution - Missense 17:7026520-7026520 + B84-Tumor COSM3932710 c.301C>A p.L101M Substitution - Missense 17:7024204-7024204 + Detroit_562 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CSCC-29-T COSM4513870 c.953C>T p.S318F Substitution - Missense 17:7026520-7026520 + S00934 COSM5662755 c.614A>T p.Q205L Substitution - Missense 17:7024613-7024613 + TCGA-A7-A4SD-01 COSM3820414 c.87C>T p.N29N Substitution - coding silent 17:7023758-7023758 + UM-SCC-2 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + CSCC-7-T COSM4459595 c.1131C>T p.I377I Substitution - coding silent 17:7026781-7026781 + TCGA-AA-3715-01 COSM4614468 c.540delC p.S183fs*20 Deletion - Frameshift 17:7024539-7024539 + TCGA-EE-A3JD-06 COSM4395247 c.473C>T p.P158L Substitution - Missense 17:7024472-7024472 + TCGA-D1-A17Q-01 COSM983704 c.524G>A p.R175Q Substitution - Missense 17:7024523-7024523 + TCGA-DK-A1A3-01 COSM417367 c.1200G>C p.R400R Substitution - coding silent 17:7026964-7026964 + T2269 COSM4665438 c.1074C>T p.C358C Substitution - coding silent 17:7026724-7026724 + TCGA-BR-4184-01 COSM4069123 c.488G>A p.R163H Substitution - Missense 17:7024487-7024487 + OSCC-GB_00140111 COSM3712430 c.393C>A p.I131I Substitution - coding silent 17:7024296-7024296 + TCGA-AA-3713-01 COSM2976084 c.1149G>A p.P383P Substitution - coding silent 17:7026799-7026799 + UD-SCC-2 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + 14T COSM3712431 c.393C>A p.I131I Substitution - coding silent 17:7024296-7024296 + TCGA-A5-A0GA-01 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + SCC-9 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-FD-A3SS-01 COSM3796015 c.28G>C p.A10P Substitution - Missense 17:7023699-7023699 + HCC2998 COSM1679445 c.115G>A p.D39N Substitution - Missense 17:7023786-7023786 + TCGA-EI-6917-01 COSM3421861 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + SCC-25 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-FS-A1ZW-06 COSM3421861 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + LIM2551 COSM4644103 c.297G>A p.S99S Substitution - coding silent 17:7024200-7024200 + TCGA-IZ-A6M9-01 COSM3989281 c.13G>T p.A5S Substitution - Missense 17:7023684-7023684 + TCGA-EI-6507-01 COSM1563668 c.1326C>T p.C442C Substitution - coding silent 17:7027505-7027505 + TCGA-DA-A1I7-06 COSM3890288 c.961C>T p.P321S Substitution - Missense 17:7026528-7026528 + WSU-HN30 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-BR-4184-01 COSM4069124 c.488G>A p.R163H Substitution - Missense 17:7024487-7024487 + TCGA-K4-A3WU-01 COSM2976067 c.871C>T p.R291W Substitution - Missense 17:7025182-7025182 + UM-SCC-47 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-BF-A3DJ-01 COSM3521502 c.970G>A p.E324K Substitution - Missense 17:7026537-7026537 + TCGA-BR-4362-01 COSM4069112 c.135C>T p.G45G Substitution - coding silent 17:7023806-7023806 + TCGA-B5-A11Y-01 COSM983716 c.1090C>T p.R364C Substitution - Missense 17:7026740-7026740 + LIM2551 COSM4644102 c.297G>A p.S99S Substitution - coding silent 17:7024200-7024200 + AOCS-086-3-2 COSM4139781 c.224T>G p.V75G Substitution - Missense 17:7024127-7024127 + TCGA-FS-A1ZA-06 COSM3421862 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + TCGA-D5-6924-01 COSM1385666 c.888G>A p.P296P Substitution - coding silent 17:7025199-7025199 + TCGA-AP-A059-01 COSM983709 c.909C>T p.C303C Substitution - coding silent 17:7026476-7026476 + TCGA-BR-4201-01 COSM4069121 c.366C>T p.H122H Substitution - coding silent 17:7024269-7024269 + TCGA-FS-A1ZW-06 COSM3421862 c.877C>T p.R293C Substitution - Missense 17:7025188-7025188 + TCGA-AZ-6601-01 COSM1385678 c.1366C>T p.R456W Substitution - Missense 17:7027545-7027545 + SCC-15 COSM983707 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + S00934 COSM5662754 c.614A>T p.Q205L Substitution - Missense 17:7024613-7024613 + TCGA-CD-A4MG-01 COSM4069130 c.960T>C p.V320V Substitution - coding silent 17:7026527-7026527 + TCGA-AZ-6601-01 COSM1385677 c.1366C>T p.R456W Substitution - Missense 17:7027545-7027545 + 8T COSM3718510 c.540C>A p.G180G Substitution - coding silent 17:7024539-7024539 + TCGA-A8-A08B-01 COSM1479932 c.967G>T p.D323Y Substitution - Missense 17:7026534-7026534 + TCGA-E9-A22G-01 COSM5833375 c.731_732delGT p.S244fs*46 Deletion - Frameshift 17:7024730-7024731 + CSCC-27-T COSM4499822 c.550C>T p.P184S Substitution - Missense 17:7024549-7024549 + TCGA-G4-6320-01 COSM3691759 c.1218C>T p.H406H Substitution - coding silent 17:7026982-7026982 + TCGA-EE-A3JD-06 COSM4395246 c.473C>T p.P158L Substitution - Missense 17:7024472-7024472 + TCGA-AP-A059-01 COSM983719 c.1290C>T p.H430H Substitution - coding silent 17:7027054-7027054 + CAL33 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-F4-6856-01 COSM1385663 c.428G>A p.R143H Substitution - Missense 17:7024427-7024427 + TCGA-HU-A4GN-01 COSM4069120 c.268G>A p.A90T Substitution - Missense 17:7024171-7024171 + 585208 COSM324809 c.946C>A p.L316M Substitution - Missense 17:7026513-7026513 + TCGA-AP-A059-01 COSM983720 c.1290C>T p.H430H Substitution - coding silent 17:7027054-7027054 + S00936 COSM308638 c.539_540insC p.S183fs*6 Insertion - Frameshift 17:7024538-7024539 + TCGA-BR-8382-01 COSM4069135 c.1367G>A p.R456Q Substitution - Missense 17:7027546-7027546 + T469 COSM4665435 c.248G>A p.G83D Substitution - Missense 17:7024151-7024151 + AOCS-130-1-0 COSM4139778 c.194C>T p.S65L Substitution - Missense 17:7024097-7024097 + TCGA-BG-A0W1-01 COSM983708 c.701_702insCAG p.S244_E245insS Insertion - In frame 17:7024700-7024701 + TCGA-F4-6856-01 COSM1385662 c.428G>A p.R143H Substitution - Missense 17:7024427-7024427 + 8T COSM3718511 c.540C>A p.G180G Substitution - coding silent 17:7024539-7024539 + LS411 COSM4614468 c.540delC p.S183fs*20 Deletion - Frameshift 17:7024539-7024539 + T3446 COSM4665436 c.404A>G p.Y135C Substitution - Missense 17:7024403-7024403 + TCGA-AP-A0LM-01 COSM983700 c.212C>T p.A71V Substitution - Missense 17:7024115-7024115 + MZ7-mel COSM21781 c.511C>T p.P171S Substitution - Missense 17:7024510-7024510 + 19M COSM5578109 c.1172C>T p.S391L Substitution - Missense 17:7026822-7026822 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.22566;Hs.22571;Hs.22575 17p13.1 608992

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T Missense p.N203Y c.607A>T 17 6927925 LUAD C A Missense p.L316M c.946C>A 17 6929832 SCLC C A Missense p.Q454K c.1360C>A 17 6930858 CM CC TT Missense p.R376C c.1125_1126delinsTT 17 6930094 CM - C Frameshift p.S183Qfs*6 c.546dupC 17 6927858 BRCA - C Frameshift p.S183Qfs*6 c.546dupC 17 6927859 SCLC C G Missense p.H378D c.1132C>G 17 6930101 CM C G Missense p.P368A c.1102C>G 17 6930071 PRAD C G Synonymous p.G88G c.264C>G 17 6927486 HNSC C T Missense p.A401V c.1202C>T 17 6930285 STAD C T Missense p.H434Y c.1300C>T 17 6930383 CM C T Missense p.P158L c.473C>T 17 6927791 CM C T Missense p.P182L c.545C>T 17 6927863 SCLC C T Missense p.P321S c.961C>T 17 6929847 CM C T Missense p.R293C c.877C>T 17 6928507 CM C T Missense p.R347C c.1039C>T 17 6929925 GBM C T Missense p.R364C c.1090C>T 17 6930059 UCEC C T Missense p.R432C c.1294C>T 17 6930377 CM C T Missense p.S279F c.836C>T 17 6928466 CM C T Synonymous p.F89F c.267C>T 17 6927489 STAD C T Synonymous p.H122H c.366C>T 17 6927588 STAD C T Synonymous p.L145L c.433C>T 17 6927751 LUSC C T Synonymous p.P84P c.252C>T 17 6927474 STAD G A Missense p.C222Y c.665G>A 17 6927983 HNSC G A Missense p.D443N c.1327G>A 17 6930825 CM G A Missense p.E324K c.970G>A 17 6929856 CM G A Missense p.G82R c.244G>A 17 6927466 UCEC G A SpliceDonorSNV . c.1323+1G>A 17 6930407 UCEC G A Synonymous p.G210G c.630G>A 17 6927948 CM G A Synonymous p.G478G c.1434G>A 17 6930932 CM G A Synonymous p.T154T c.462G>A 17 6927780 CM G C Missense p.E437Q c.1309G>C 17 6930392 HNSC G C Synonymous p.R400R c.1200G>C 17 6930283 BLCA GG AA Missense p.G380R c.1137_1138delinsAA 17 6930106 CM G T Missense p.D323Y c.967G>T 17 6929853 BRCA G T Nonsense p.E299* c.895G>T 17 6929781 LUAD G T Synonymous p.G478G c.1434G>T 17 6930932 HNSC T C Synonymous p.A269A c.807T>C 17 6928437 COREAD