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 11 65365763 65365763 + 5'Flank SNP C C G TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr11:65365763C>G BLCA 11 65375760 65375760 + Missense_Mutation SNP G G A TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr11:65375760G>A c.128C>T c.(127-129)tCt>tTt p.S43F BLCA 11 65375774 65375774 + Silent SNP C C T TCGA-E7-A3Y1-01A-11D-A22Z-08 TCGA-E7-A3Y1-10A-01D-A22Z-08 g.chr11:65375774C>T c.114G>A c.(112-114)aaG>aaA p.K38K BLCA 11 65380753 65380753 + 5'Flank SNP C C A TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr11:65380753C>A BLCA 11 65380813 65380813 + 5'Flank SNP C C T TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr11:65380813C>T BLCA 11 65381077 65381077 + 5'Flank SNP C C G TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr11:65381077C>G BRCA 11 65365763 65365763 + 5'Flank SNP C C G TCGA-AO-A03V-01A-11D-A10Y-09 TCGA-AO-A03V-10A-01D-A110-09 g.chr11:65365763C>G BRCA 11 65365835 65365835 + 5'Flank DEL C C - TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr11:65365835delC BRCA 11 65374961 65374961 + Silent SNP C C T TCGA-D8-A13Y-01A-11D-A10Y-09 TCGA-D8-A13Y-10A-01D-A110-09 g.chr11:65374961C>T c.498G>A c.(496-498)gaG>gaA p.E166E BRCA 11 65380777 65380777 + 5'Flank SNP C C T TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr11:65380777C>T BRCA 11 65380870 65380870 + 5'Flank SNP C C A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr11:65380870C>A CESC 11 65375232 65375232 + Silent SNP C C T TCGA-JW-A5VK-01A-11D-A28B-09 TCGA-JW-A5VK-10A-01D-A28E-09 g.chr11:65375232C>T c.354G>A c.(352-354)caG>caA p.Q118Q CHOL 11 65373425 65373425 + Missense_Mutation SNP C C G TCGA-3X-AAV9-01A-72D-A417-09 TCGA-3X-AAV9-10A-01D-A41A-09 g.chr11:65373425C>G c.960G>C c.(958-960)caG>caC p.Q320H COAD 11 65365834 65365835 + 5'Flank INS - - C TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:65365834_65365835insC COAD 11 65365955 65365955 + 5'Flank SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:65365955G>A COAD 11 65365977 65365977 + 5'Flank SNP C C A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:65365977C>A COAD 11 65366066 65366066 + 5'Flank SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:65366066C>T COAD 11 65366078 65366078 + 5'Flank SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr11:65366078G>A COAD 11 65366866 65366866 + Splice_Site SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:65366866G>A c.1434C>T c.(1432-1434)cgC>cgT p.R478R COAD 11 65366953 65366953 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:65366953C>T c.1347G>A c.(1345-1347)ccG>ccA p.P449P COAD 11 65366954 65366954 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:65366954G>A c.1346C>T c.(1345-1347)cCg>cTg p.P449L COAD 11 65367034 65367034 + Frame_Shift_Del DEL G G - TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr11:65367034delG c.1266delC c.(1264-1266)cccfs p.P422fs COAD 11 65373508 65373508 + Frame_Shift_Del DEL G G - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:65373508delG c.877delC c.(877-879)cgafs p.R294fs COAD 11 65375277 65375277 + Silent SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:65375277C>T c.309G>A c.(307-309)gcG>gcA p.A103A COAD 11 65375494 65375494 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:65375494C>T c.197G>A c.(196-198)cGt>cAt p.R66H COAD 11 65380572 65380572 + 5'Flank SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:65380572G>A COAD 11 65380789 65380789 + 5'Flank SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr11:65380789G>A COADREAD 11 65365834 65365835 + 5'Flank INS - - C TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:65365834_65365835insC COADREAD 11 65365955 65365955 + 5'Flank SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:65365955G>A COADREAD 11 65365977 65365977 + 5'Flank SNP C C A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:65365977C>A COADREAD 11 65366066 65366066 + 5'Flank SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:65366066C>T COADREAD 11 65366078 65366078 + 5'Flank SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr11:65366078G>A COADREAD 11 65366866 65366866 + Splice_Site SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:65366866G>A c.1434C>T c.(1432-1434)cgC>cgT p.R478R COADREAD 11 65366953 65366953 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:65366953C>T c.1347G>A c.(1345-1347)ccG>ccA p.P449P COADREAD 11 65366954 65366954 + Missense_Mutation SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:65366954G>A c.1346C>T c.(1345-1347)cCg>cTg p.P449L COADREAD 11 65367034 65367034 + Frame_Shift_Del DEL G G - TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr11:65367034delG c.1266delC c.(1264-1266)cccfs p.P422fs COADREAD 11 65373508 65373508 + Frame_Shift_Del DEL G G - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:65373508delG c.877delC c.(877-879)cgafs p.R294fs COADREAD 11 65375277 65375277 + Silent SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:65375277C>T c.309G>A c.(307-309)gcG>gcA p.A103A COADREAD 11 65375494 65375494 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:65375494C>T c.197G>A c.(196-198)cGt>cAt p.R66H COADREAD 11 65380572 65380572 + 5'Flank SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:65380572G>A COADREAD 11 65380783 65380783 + 5'Flank SNP C C T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr11:65380783C>T COADREAD 11 65380789 65380789 + 5'Flank SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr11:65380789G>A DLBC 11 65367223 65367223 + Silent SNP A A G TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr11:65367223A>G c.1077T>C c.(1075-1077)ccT>ccC p.P359P DLBC 11 65373249 65373249 + Missense_Mutation SNP G G T TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr11:65373249G>T c.1043C>A c.(1042-1044)aCa>aAa p.T348K ESCA 11 65373507 65373507 + Missense_Mutation SNP C C T TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr11:65373507C>T c.878G>A c.(877-879)cGa>cAa p.R293Q ESCA 11 65374944 65374944 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr11:65374944C>T c.515G>A c.(514-516)cGc>cAc p.R172H ESCA 11 65375494 65375494 + Missense_Mutation SNP C C T TCGA-VR-AA4D-01A-11D-A37C-09 TCGA-VR-AA4D-10A-01D-A37F-09 g.chr11:65375494C>T c.197G>A c.(196-198)cGt>cAt p.R66H ESCA 11 65380856 65380856 + 5'Flank SNP G G A TCGA-L5-A4OG-01A-11D-A27G-09 TCGA-L5-A4OG-11A-12D-A27G-09 g.chr11:65380856G>A GBM 11 65367001 65367001 + Silent SNP C C A TCGA-28-5214-01A-01D-1486-08 TCGA-28-5214-10A-01D-1486-08 g.chr11:65367001C>A c.1299G>T c.(1297-1299)ccG>ccT p.P433P GBM 11 65375157 65375157 + Silent SNP C C T TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr11:65375157C>T c.429G>A c.(427-429)aaG>aaA p.K143K GBMLGG 11 65366003 65366003 + 5'Flank SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65366003C>T GBMLGG 11 65367001 65367001 + Silent SNP C C A TCGA-28-5214-01A-01D-1486-08 TCGA-28-5214-10A-01D-1486-08 g.chr11:65367001C>A c.1299G>T c.(1297-1299)ccG>ccT p.P433P GBMLGG 11 65375157 65375157 + Silent SNP C C T TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr11:65375157C>T c.429G>A c.(427-429)aaG>aaA p.K143K HNSC 11 65365776 65365776 + 5'Flank SNP C C T TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr11:65365776C>T HNSC 11 65367018 65367019 + Frame_Shift_Del DEL GC GC - TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr11:65367018_65367019delGC c.1281_1282delGC c.(1279-1284)gcgcccfs p.P428fs HNSC 11 65375418 65375418 + Frame_Shift_Del DEL G G - TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr11:65375418delG c.273delC c.(271-273)cccfs p.P91fs HNSC 11 65375490 65375490 + Silent SNP G G C TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr11:65375490G>C c.201C>G c.(199-201)ggC>ggG p.G67G HNSC 11 65380600 65380600 + 5'Flank SNP C C T TCGA-CV-5431-01A-01D-1512-08 TCGA-CV-5431-11A-01D-1512-08 g.chr11:65380600C>T HNSC 11 65380700 65380700 + 5'Flank SNP G G T TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chr11:65380700G>T KIPAN 11 65375920 65375920 + Splice_Site SNP C C A TCGA-BP-5194-01A-02D-1429-08 TCGA-BP-5194-11A-01D-1429-08 g.chr11:65375920C>A c.e2-1 KIPAN 11 65380540 65380540 + 5'Flank SNP G G A TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chr11:65380540G>A KIRC 11 65375920 65375920 + Splice_Site SNP C C A TCGA-BP-5194-01A-02D-1429-08 TCGA-BP-5194-11A-01D-1429-08 g.chr11:65375920C>A c.e2-1 KIRC 11 65380540 65380540 + 5'Flank SNP G G A TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chr11:65380540G>A LGG 11 65366003 65366003 + 5'Flank SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65366003C>T LIHC 11 65365864 65365864 + 5'Flank SNP G G T TCGA-5R-AA1C-01A-11D-A40R-10 TCGA-5R-AA1C-10A-01D-A40U-10 g.chr11:65365864G>T LIHC 11 65365896 65365896 + 5'Flank SNP T T C TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr11:65365896T>C LIHC 11 65373551 65373551 + Splice_Site SNP C C T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:65373551C>T c.834G>A c.(832-834)ttG>ttA p.L278L LIHC 11 65380603 65380603 + 5'Flank SNP G G A TCGA-XR-A8TD-01A-12D-A38X-10 TCGA-XR-A8TD-10A-01D-A38X-10 g.chr11:65380603G>A LIHC 11 65380716 65380716 + 5'Flank SNP A A T TCGA-G3-A5SL-01A-11D-A27I-10 TCGA-G3-A5SL-10A-01D-A27I-10 g.chr11:65380716A>T LUAD 11 65365945 65365945 + 5'Flank SNP C C A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr11:65365945C>A LUAD 11 65365946 65365946 + 5'Flank SNP C C A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr11:65365946C>A LUAD 11 65373321 65373321 + Missense_Mutation SNP C C T TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr11:65373321C>T c.971G>A c.(970-972)aGa>aAa p.R324K LUAD 11 65375118 65375118 + Missense_Mutation SNP C C G TCGA-38-6178-01A-11D-1753-08 TCGA-38-6178-10A-01D-1753-08 g.chr11:65375118C>G c.468G>C c.(466-468)aaG>aaC p.K156N LUAD 11 65375408 65375408 + Missense_Mutation SNP C C A TCGA-50-5936-01A-11D-1625-08 TCGA-50-5936-11A-01D-1625-08 g.chr11:65375408C>A c.283G>T c.(283-285)Gca>Tca p.A95S LUAD 11 65375749 65375749 + Missense_Mutation SNP C C T TCGA-05-5423-01A-01D-1625-08 TCGA-05-5423-10A-01D-1625-08 g.chr11:65375749C>T c.139G>A c.(139-141)Gac>Aac p.D47N LUAD 11 65380566 65380566 + 5'Flank SNP T T C TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:65380566T>C LUAD 11 65380732 65380732 + 5'Flank SNP G G C TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr11:65380732G>C LUSC 11 65373256 65373256 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:65373256G>A c.1036C>T c.(1036-1038)Cct>Tct p.P346S LUSC 11 65375242 65375242 + Missense_Mutation SNP A A G TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr11:65375242A>G c.344T>C c.(343-345)aTc>aCc p.I115T LUSC 11 65375870 65375870 + Silent SNP C C T TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr11:65375870C>T c.18G>A c.(16-18)ctG>ctA p.L6L PRAD 11 65365835 65365835 + 5'Flank DEL C C - TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr11:65365835delC PRAD 11 65366866 65366866 + Splice_Site SNP G G A TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr11:65366866G>A c.1434C>T c.(1432-1434)cgC>cgT p.R478R PRAD 11 65375265 65375265 + Silent SNP G G A TCGA-HC-8266-01A-11D-2260-08 TCGA-HC-8266-10A-01D-2260-08 g.chr11:65375265G>A c.321C>T c.(319-321)caC>caT p.H107H READ 11 65380783 65380783 + 5'Flank SNP C C T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr11:65380783C>T SARC 11 65374848 65374848 + Missense_Mutation SNP A A T TCGA-DX-A6B8-01A-11D-A307-09 TCGA-DX-A6B8-10A-01D-A307-09 g.chr11:65374848A>T c.611T>A c.(610-612)cTg>cAg p.L204Q SARC 11 65381110 65381110 + 5'Flank SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:65381110C>T SKCM 11 65366005 65366005 + 5'Flank SNP A A T TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr11:65366005A>T SKCM 11 65366868 65366868 + Missense_Mutation SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr11:65366868G>A c.1432C>T c.(1432-1434)Cgc>Tgc p.R478C SKCM 11 65366992 65366992 + Silent SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr11:65366992G>A c.1308C>T c.(1306-1308)tcC>tcT p.S436S SKCM 11 65367008 65367008 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:65367008G>A c.1292C>T c.(1291-1293)aCc>aTc p.T431I SKCM 11 65367011 65367011 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr11:65367011G>A c.1289C>T c.(1288-1290)cCg>cTg p.P430L SKCM 11 65367187 65367187 + Silent SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr11:65367187G>A c.1113C>T c.(1111-1113)ccC>ccT p.P371P SKCM 11 65367188 65367188 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr11:65367188G>A c.1112C>T c.(1111-1113)cCc>cTc p.P371L SKCM 11 65373427 65373427 + Nonsense_Mutation SNP G G A TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr11:65373427G>A c.958C>T c.(958-960)Cag>Tag p.Q320* SKCM 11 65373447 65373447 + Missense_Mutation SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr11:65373447G>A c.938C>T c.(937-939)tCc>tTc p.S313F SKCM 11 65373509 65373509 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:65373509G>A c.876C>T c.(874-876)ccC>ccT p.P292P SKCM 11 65374967 65374967 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr11:65374967C>T c.492G>A c.(490-492)gaG>gaA p.E164E SKCM 11 65375207 65375207 + Silent SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr11:65375207G>A c.379C>T c.(379-381)Cta>Tta p.L127L SKCM 11 65375744 65375744 + Silent SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr11:65375744G>A c.144C>T c.(142-144)gtC>gtT p.V48V SKCM 11 65380868 65380868 + 5'Flank SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr11:65380868C>T

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 11 65360538 65360538 single base substitution C T downstream_gene_variant BLCA-US 11 65360568 65360568 single base substitution C T downstream_gene_variant BLCA-US 11 65363055 65363055 single base substitution C A downstream_gene_variant BLCA-US 11 65375774 65375774 single base substitution C T downstream_gene_variant BLCA-US 11 65375774 65375774 single base substitution C T exon_variant BLCA-US 11 65375774 65375774 single base substitution C T synonymous_variant K295K 885G>A BLCA-US 11 65375774 65375774 single base substitution C T synonymous_variant K38K 114G>A BLCA-US 11 65375774 65375774 single base substitution C T synonymous_variant K45K 135G>A BLCA-US 11 65375774 65375774 single base substitution C T upstream_gene_variant BLCA-US 11 65385501 65385501 single base substitution A G upstream_gene_variant BRCA-EU 11 65360317 65360317 single base substitution T C downstream_gene_variant BRCA-EU 11 65363393 65363393 single base substitution G C downstream_gene_variant BRCA-EU 11 65364022 65364022 single base substitution C T downstream_gene_variant BRCA-EU 11 65367211 65367211 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 65367211 65367211 single base substitution G A exon_variant BRCA-EU 11 65367211 65367211 single base substitution G A synonymous_variant P363P 1089C>T BRCA-EU 11 65367211 65367211 single base substitution G A synonymous_variant P36P 108C>T BRCA-EU 11 65367211 65367211 single base substitution G A synonymous_variant P620P 1860C>T BRCA-EU 11 65368007 65368007 single base substitution A G intron_variant BRCA-EU 11 65368533 65368533 single base substitution C A downstream_gene_variant BRCA-EU 11 65368533 65368533 single base substitution C A intron_variant BRCA-EU 11 65368805 65368805 single base substitution C A downstream_gene_variant BRCA-EU 11 65368805 65368805 single base substitution C A intron_variant BRCA-EU 11 65369293 65369293 single base substitution G A downstream_gene_variant BRCA-EU 11 65369293 65369293 single base substitution G A intron_variant BRCA-EU 11 65372163 65372163 single base substitution C G downstream_gene_variant BRCA-EU 11 65372163 65372163 single base substitution C G intron_variant BRCA-EU 11 65372859 65372859 single base substitution C T downstream_gene_variant BRCA-EU 11 65372859 65372859 single base substitution C T intron_variant BRCA-EU 11 65373550 65373550 single base substitution C G downstream_gene_variant BRCA-EU 11 65373550 65373550 single base substitution C G exon_variant BRCA-EU 11 65373550 65373550 single base substitution C G missense_variant E279Q 835G>C BRCA-EU 11 65373550 65373550 single base substitution C G missense_variant E536Q 1606G>C BRCA-EU 11 65373550 65373550 single base substitution C G splice_region_variant BRCA-EU 11 65373661 65373661 single base substitution C A downstream_gene_variant BRCA-EU 11 65373661 65373661 single base substitution C A exon_variant BRCA-EU 11 65373661 65373661 single base substitution C A intron_variant BRCA-EU 11 65373977 65373977 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 65373977 65373977 deletion of <=200bp A - exon_variant BRCA-EU 11 65373977 65373977 deletion of <=200bp A - intron_variant BRCA-EU 11 65373977 65373977 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 65374124 65374124 deletion of <=200bp G - downstream_gene_variant BRCA-EU 11 65374124 65374124 deletion of <=200bp G - exon_variant BRCA-EU 11 65374124 65374124 deletion of <=200bp G - intron_variant BRCA-EU 11 65374124 65374124 deletion of <=200bp G - upstream_gene_variant BRCA-EU 11 65374130 65374130 single base substitution C T downstream_gene_variant BRCA-EU 11 65374130 65374130 single base substitution C T exon_variant BRCA-EU 11 65374130 65374130 single base substitution C T intron_variant BRCA-EU 11 65374130 65374130 single base substitution C T upstream_gene_variant BRCA-EU 11 65374229 65374229 single base substitution C A 3_prime_UTR_variant BRCA-EU 11 65374229 65374229 single base substitution C A 5_prime_UTR_variant BRCA-EU 11 65374229 65374229 single base substitution C A downstream_gene_variant BRCA-EU 11 65374229 65374229 single base substitution C A exon_variant BRCA-EU 11 65374229 65374229 single base substitution C A synonymous_variant R255R 765G>T BRCA-EU 11 65374229 65374229 single base substitution C A synonymous_variant R512R 1536G>T BRCA-EU 11 65374229 65374229 single base substitution C A upstream_gene_variant BRCA-EU 11 65375487 65375487 single base substitution A T downstream_gene_variant BRCA-EU 11 65375487 65375487 single base substitution A T exon_variant BRCA-EU 11 65375487 65375487 single base substitution A T synonymous_variant I325I 975T>A BRCA-EU 11 65375487 65375487 single base substitution A T synonymous_variant I68I 204T>A BRCA-EU 11 65375487 65375487 single base substitution A T synonymous_variant I75I 225T>A BRCA-EU 11 65375487 65375487 single base substitution A T upstream_gene_variant BRCA-EU 11 65380049 65380049 single base substitution G C exon_variant BRCA-EU 11 65380049 65380049 single base substitution G C intron_variant BRCA-EU 11 65380049 65380049 single base substitution G C upstream_gene_variant BRCA-EU 11 65380077 65380077 single base substitution G T exon_variant BRCA-EU 11 65380077 65380077 single base substitution G T intron_variant BRCA-EU 11 65380077 65380077 single base substitution G T upstream_gene_variant BRCA-EU 11 65384526 65384526 single base substitution G T upstream_gene_variant BRCA-EU 11 65386319 65386319 single base substitution A C upstream_gene_variant BRCA-FR 11 65368805 65368805 single base substitution C A downstream_gene_variant BRCA-FR 11 65368805 65368805 single base substitution C A intron_variant BRCA-FR 11 65380276 65380276 single base substitution C G exon_variant BRCA-FR 11 65380276 65380276 single base substitution C G intron_variant BRCA-FR 11 65380276 65380276 single base substitution C G upstream_gene_variant BRCA-FR 11 65382187 65382187 single base substitution C T exon_variant BRCA-FR 11 65382187 65382187 single base substitution C T upstream_gene_variant BRCA-UK 11 65372859 65372859 single base substitution C T downstream_gene_variant BRCA-UK 11 65372859 65372859 single base substitution C T intron_variant BRCA-US 11 65360593 65360593 single base substitution G C downstream_gene_variant BRCA-US 11 65365763 65365763 single base substitution C G 3_prime_UTR_variant BRCA-US 11 65365763 65365763 single base substitution C G downstream_gene_variant BRCA-US 11 65365763 65365763 single base substitution C G stop_lost *264S 791G>C BRCA-US 11 65365763 65365763 single base substitution C G stop_lost *591S 1772G>C BRCA-US 11 65365763 65365763 single base substitution C G stop_lost *848S 2543G>C BRCA-US 11 65365835 65365835 deletion of <=200bp C - 3_prime_UTR_variant BRCA-US 11 65365835 65365835 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G240 BRCA-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G567 BRCA-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G824 BRCA-US 11 65374961 65374961 single base substitution C T downstream_gene_variant BRCA-US 11 65374961 65374961 single base substitution C T exon_variant BRCA-US 11 65374961 65374961 single base substitution C T synonymous_variant E166E 498G>A BRCA-US 11 65374961 65374961 single base substitution C T synonymous_variant E423E 1269G>A BRCA-US 11 65374961 65374961 single base substitution C T upstream_gene_variant BRCA-US 11 65380777 65380777 single base substitution C T exon_variant BRCA-US 11 65380777 65380777 single base substitution C T intron_variant BRCA-US 11 65380777 65380777 single base substitution C T missense_variant D151N 451G>A BRCA-US 11 65380777 65380777 single base substitution C T upstream_gene_variant BRCA-US 11 65380870 65380870 single base substitution C A exon_variant BRCA-US 11 65380870 65380870 single base substitution C A intron_variant BRCA-US 11 65380870 65380870 single base substitution C A stop_gained E120* 358G>T BRCA-US 11 65380870 65380870 single base substitution C A upstream_gene_variant BRCA-US 11 65384451 65384451 single base substitution G C upstream_gene_variant BRCA-US 11 65384757 65384757 single base substitution C G upstream_gene_variant BRCA-US 11 65384797 65384797 single base substitution G C upstream_gene_variant BRCA-US 11 65387069 65387069 single base substitution G A upstream_gene_variant BTCA-JP 11 65361257 65361257 single base substitution G T downstream_gene_variant BTCA-JP 11 65363317 65363317 single base substitution C A downstream_gene_variant BTCA-JP 11 65367001 65367001 single base substitution C T 3_prime_UTR_variant BTCA-JP 11 65367001 65367001 single base substitution C T exon_variant BTCA-JP 11 65367001 65367001 single base substitution C T synonymous_variant P106P 318G>A BTCA-JP 11 65367001 65367001 single base substitution C T synonymous_variant P433P 1299G>A BTCA-JP 11 65367001 65367001 single base substitution C T synonymous_variant P690P 2070G>A BTCA-JP 11 65374926 65374926 single base substitution G A downstream_gene_variant BTCA-JP 11 65374926 65374926 single base substitution G A exon_variant BTCA-JP 11 65374926 65374926 single base substitution G A missense_variant A178V 533C>T BTCA-JP 11 65374926 65374926 single base substitution G A missense_variant A435V 1304C>T BTCA-JP 11 65374926 65374926 single base substitution G A upstream_gene_variant BTCA-JP 11 65374945 65374945 single base substitution G A downstream_gene_variant BTCA-JP 11 65374945 65374945 single base substitution G A exon_variant BTCA-JP 11 65374945 65374945 single base substitution G A missense_variant R172C 514C>T BTCA-JP 11 65374945 65374945 single base substitution G A missense_variant R429C 1285C>T BTCA-JP 11 65374945 65374945 single base substitution G A upstream_gene_variant BTCA-JP 11 65375777 65375777 single base substitution G A downstream_gene_variant BTCA-JP 11 65375777 65375777 single base substitution G A exon_variant BTCA-JP 11 65375777 65375777 single base substitution G A synonymous_variant I294I 882C>T BTCA-JP 11 65375777 65375777 single base substitution G A synonymous_variant I37I 111C>T BTCA-JP 11 65375777 65375777 single base substitution G A synonymous_variant I44I 132C>T BTCA-JP 11 65375777 65375777 single base substitution G A upstream_gene_variant BTCA-JP 11 65380628 65380628 single base substitution G A exon_variant BTCA-JP 11 65380628 65380628 single base substitution G A intron_variant BTCA-JP 11 65380628 65380628 single base substitution G A synonymous_variant P200P 600C>T BTCA-JP 11 65380628 65380628 single base substitution G A upstream_gene_variant BTCA-JP 11 65385461 65385461 single base substitution G C upstream_gene_variant BTCA-JP 11 65385705 65385705 single base substitution C T upstream_gene_variant BTCA-JP 11 65385743 65385743 single base substitution G A upstream_gene_variant BTCA-JP 11 65387818 65387818 single base substitution C T upstream_gene_variant CESC-US 11 65375232 65375232 single base substitution C T downstream_gene_variant CESC-US 11 65375232 65375232 single base substitution C T exon_variant CESC-US 11 65375232 65375232 single base substitution C T intron_variant CESC-US 11 65375232 65375232 single base substitution C T synonymous_variant Q118Q 354G>A CESC-US 11 65375232 65375232 single base substitution C T synonymous_variant Q375Q 1125G>A CESC-US 11 65375232 65375232 single base substitution C T upstream_gene_variant CESC-US 11 65383829 65383829 single base substitution C T upstream_gene_variant CLLE-ES 11 65371735 65371735 single base substitution G A downstream_gene_variant CLLE-ES 11 65371735 65371735 single base substitution G A intron_variant COAD-US 11 65360924 65360924 single base substitution C T downstream_gene_variant COAD-US 11 65361059 65361059 single base substitution G A downstream_gene_variant COAD-US 11 65361256 65361256 single base substitution C T downstream_gene_variant COAD-US 11 65361321 65361321 single base substitution G A downstream_gene_variant COAD-US 11 65363022 65363022 single base substitution C T downstream_gene_variant COAD-US 11 65363148 65363148 single base substitution C A downstream_gene_variant COAD-US 11 65363227 65363227 single base substitution G A downstream_gene_variant COAD-US 11 65365834 65365834 insertion of <=200bp - C 3_prime_UTR_variant COAD-US 11 65365834 65365834 insertion of <=200bp - C downstream_gene_variant COAD-US 11 65365834 65365834 insertion of <=200bp - C frameshift_variant G240G? COAD-US 11 65365834 65365834 insertion of <=200bp - C frameshift_variant G567G? COAD-US 11 65365834 65365834 insertion of <=200bp - C frameshift_variant G824G? COAD-US 11 65365955 65365955 single base substitution G A 3_prime_UTR_variant COAD-US 11 65365955 65365955 single base substitution G A downstream_gene_variant COAD-US 11 65365955 65365955 single base substitution G A missense_variant A200V 599C>T COAD-US 11 65365955 65365955 single base substitution G A missense_variant A527V 1580C>T COAD-US 11 65365955 65365955 single base substitution G A missense_variant A784V 2351C>T COAD-US 11 65366066 65366066 single base substitution C T downstream_gene_variant COAD-US 11 65366066 65366066 single base substitution C T intron_variant COAD-US 11 65366066 65366066 single base substitution C T missense_variant R163H 488G>A COAD-US 11 65366066 65366066 single base substitution C T missense_variant R490H 1469G>A COAD-US 11 65366066 65366066 single base substitution C T missense_variant R747H 2240G>A COAD-US 11 65366078 65366078 single base substitution G A downstream_gene_variant COAD-US 11 65366078 65366078 single base substitution G A intron_variant COAD-US 11 65366078 65366078 single base substitution G A missense_variant P159L 476C>T COAD-US 11 65366078 65366078 single base substitution G A missense_variant P486L 1457C>T COAD-US 11 65366078 65366078 single base substitution G A missense_variant P743L 2228C>T COAD-US 11 65366866 65366866 single base substitution G A downstream_gene_variant COAD-US 11 65366866 65366866 single base substitution G A splice_region_variant COAD-US 11 65366953 65366953 single base substitution C T 3_prime_UTR_variant COAD-US 11 65366953 65366953 single base substitution C T exon_variant COAD-US 11 65366953 65366953 single base substitution C T synonymous_variant P122P 366G>A COAD-US 11 65366953 65366953 single base substitution C T synonymous_variant P449P 1347G>A COAD-US 11 65366953 65366953 single base substitution C T synonymous_variant P706P 2118G>A COAD-US 11 65366954 65366954 single base substitution G A 3_prime_UTR_variant COAD-US 11 65366954 65366954 single base substitution G A exon_variant COAD-US 11 65366954 65366954 single base substitution G A missense_variant P122L 365C>T COAD-US 11 65366954 65366954 single base substitution G A missense_variant P449L 1346C>T COAD-US 11 65366954 65366954 single base substitution G A missense_variant P706L 2117C>T COAD-US 11 65367022 65367022 single base substitution G A 3_prime_UTR_variant COAD-US 11 65367022 65367022 single base substitution G A exon_variant COAD-US 11 65367022 65367022 single base substitution G A synonymous_variant P426P 1278C>T COAD-US 11 65367022 65367022 single base substitution G A synonymous_variant P683P 2049C>T COAD-US 11 65367022 65367022 single base substitution G A synonymous_variant P99P 297C>T COAD-US 11 65373508 65373508 deletion of <=200bp G - 3_prime_UTR_variant COAD-US 11 65373508 65373508 deletion of <=200bp G - 5_prime_UTR_variant COAD-US 11 65373508 65373508 deletion of <=200bp G - downstream_gene_variant COAD-US 11 65373508 65373508 deletion of <=200bp G - exon_variant COAD-US 11 65373508 65373508 deletion of <=200bp G - frameshift_variant R293 COAD-US 11 65373508 65373508 deletion of <=200bp G - frameshift_variant R550 COAD-US 11 65375277 65375277 single base substitution C T downstream_gene_variant COAD-US 11 65375277 65375277 single base substitution C T exon_variant COAD-US 11 65375277 65375277 single base substitution C T intron_variant COAD-US 11 65375277 65375277 single base substitution C T synonymous_variant A103A 309G>A COAD-US 11 65375277 65375277 single base substitution C T synonymous_variant A110A 330G>A COAD-US 11 65375277 65375277 single base substitution C T synonymous_variant A360A 1080G>A COAD-US 11 65375277 65375277 single base substitution C T upstream_gene_variant COAD-US 11 65380572 65380572 single base substitution G A exon_variant COAD-US 11 65380572 65380572 single base substitution G A intron_variant COAD-US 11 65380572 65380572 single base substitution G A missense_variant A219V 656C>T COAD-US 11 65380572 65380572 single base substitution G A upstream_gene_variant COAD-US 11 65383815 65383815 deletion of <=200bp G - upstream_gene_variant COAD-US 11 65384727 65384727 single base substitution C T upstream_gene_variant COAD-US 11 65386001 65386001 single base substitution C T upstream_gene_variant COAD-US 11 65386151 65386151 single base substitution C T upstream_gene_variant COAD-US 11 65386336 65386336 single base substitution C T upstream_gene_variant COAD-US 11 65386339 65386339 single base substitution T G upstream_gene_variant COAD-US 11 65386484 65386484 single base substitution G A upstream_gene_variant COAD-US 11 65387815 65387815 single base substitution C T upstream_gene_variant COCA-CN 11 65364777 65364777 single base substitution G T downstream_gene_variant COCA-CN 11 65374214 65374214 single base substitution G A 3_prime_UTR_variant COCA-CN 11 65374214 65374214 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 11 65374214 65374214 single base substitution G A downstream_gene_variant COCA-CN 11 65374214 65374214 single base substitution G A exon_variant COCA-CN 11 65374214 65374214 single base substitution G A synonymous_variant F260F 780C>T COCA-CN 11 65374214 65374214 single base substitution G A synonymous_variant F517F 1551C>T COCA-CN 11 65374214 65374214 single base substitution G A upstream_gene_variant COCA-CN 11 65374263 65374263 single base substitution C T 5_prime_UTR_variant COCA-CN 11 65374263 65374263 single base substitution C T downstream_gene_variant COCA-CN 11 65374263 65374263 single base substitution C T exon_variant COCA-CN 11 65374263 65374263 single base substitution C T missense_variant R244H 731G>A COCA-CN 11 65374263 65374263 single base substitution C T missense_variant R501H 1502G>A COCA-CN 11 65374263 65374263 single base substitution C T upstream_gene_variant COCA-CN 11 65374735 65374735 single base substitution C A downstream_gene_variant COCA-CN 11 65374735 65374735 single base substitution C A exon_variant COCA-CN 11 65374735 65374735 single base substitution C A splice_region_variant COCA-CN 11 65374735 65374735 single base substitution C A upstream_gene_variant COCA-CN 11 65375383 65375383 single base substitution G A downstream_gene_variant COCA-CN 11 65375383 65375383 single base substitution G A exon_variant COCA-CN 11 65375383 65375383 single base substitution G A intron_variant COCA-CN 11 65375383 65375383 single base substitution G A upstream_gene_variant COCA-CN 11 65384808 65384808 single base substitution C A upstream_gene_variant COCA-CN 11 65385884 65385884 single base substitution G A upstream_gene_variant COCA-CN 11 65387781 65387781 single base substitution G A upstream_gene_variant ESAD-UK 11 65362289 65362289 single base substitution C G downstream_gene_variant ESAD-UK 11 65366006 65366006 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 65366006 65366006 single base substitution G A downstream_gene_variant ESAD-UK 11 65366006 65366006 single base substitution G A missense_variant P183L 548C>T ESAD-UK 11 65366006 65366006 single base substitution G A missense_variant P510L 1529C>T ESAD-UK 11 65366006 65366006 single base substitution G A missense_variant P767L 2300C>T ESAD-UK 11 65368475 65368475 single base substitution C A downstream_gene_variant ESAD-UK 11 65368475 65368475 single base substitution C A intron_variant ESAD-UK 11 65369341 65369341 single base substitution C T downstream_gene_variant ESAD-UK 11 65369341 65369341 single base substitution C T intron_variant ESAD-UK 11 65374241 65374241 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 11 65374241 65374241 single base substitution G A downstream_gene_variant ESAD-UK 11 65374241 65374241 single base substitution G A exon_variant ESAD-UK 11 65374241 65374241 single base substitution G A synonymous_variant P251P 753C>T ESAD-UK 11 65374241 65374241 single base substitution G A synonymous_variant P508P 1524C>T ESAD-UK 11 65374241 65374241 single base substitution G A upstream_gene_variant ESAD-UK 11 65375067 65375067 single base substitution C A downstream_gene_variant ESAD-UK 11 65375067 65375067 single base substitution C A intron_variant ESAD-UK 11 65375067 65375067 single base substitution C A upstream_gene_variant ESAD-UK 11 65381906 65381906 single base substitution C G exon_variant ESAD-UK 11 65381906 65381906 single base substitution C G upstream_gene_variant ESAD-UK 11 65382595 65382595 single base substitution G A exon_variant ESAD-UK 11 65382595 65382595 single base substitution G A upstream_gene_variant ESAD-UK 11 65385029 65385029 single base substitution C T upstream_gene_variant ESAD-UK 11 65386832 65386832 single base substitution T A upstream_gene_variant ESAD-UK 11 65386833 65386833 single base substitution C A upstream_gene_variant ESAD-UK 11 65387588 65387588 single base substitution A C upstream_gene_variant GBM-US 11 65367001 65367001 single base substitution C A 3_prime_UTR_variant GBM-US 11 65367001 65367001 single base substitution C A exon_variant GBM-US 11 65367001 65367001 single base substitution C A synonymous_variant P106P 318G>T GBM-US 11 65367001 65367001 single base substitution C A synonymous_variant P433P 1299G>T GBM-US 11 65367001 65367001 single base substitution C A synonymous_variant P690P 2070G>T GBM-US 11 65375157 65375157 single base substitution C T downstream_gene_variant GBM-US 11 65375157 65375157 single base substitution C T exon_variant GBM-US 11 65375157 65375157 single base substitution C T synonymous_variant K143K 429G>A GBM-US 11 65375157 65375157 single base substitution C T synonymous_variant K400K 1200G>A GBM-US 11 65375157 65375157 single base substitution C T upstream_gene_variant GBM-US 11 65381159 65381159 single base substitution A C exon_variant GBM-US 11 65381159 65381159 single base substitution A C intron_variant GBM-US 11 65381159 65381159 single base substitution A C synonymous_variant G23G 69T>G GBM-US 11 65381159 65381159 single base substitution A C upstream_gene_variant KIRC-US 11 65375920 65375920 single base substitution C A downstream_gene_variant KIRC-US 11 65375920 65375920 single base substitution C A exon_variant KIRC-US 11 65375920 65375920 single base substitution C A intron_variant KIRC-US 11 65375920 65375920 single base substitution C A splice_acceptor_variant KIRC-US 11 65375920 65375920 single base substitution C A upstream_gene_variant KIRC-US 11 65384727 65384727 single base substitution C T upstream_gene_variant KIRC-US 11 65386188 65386188 single base substitution G A upstream_gene_variant LAML-KR 11 65364639 65364639 single base substitution A T downstream_gene_variant LAML-KR 11 65364796 65364796 single base substitution C T downstream_gene_variant LAML-KR 11 65364804 65364804 single base substitution T C downstream_gene_variant LICA-CN 11 65365898 65365898 single base substitution C A 3_prime_UTR_variant LICA-CN 11 65365898 65365898 single base substitution C A downstream_gene_variant LICA-CN 11 65365898 65365898 single base substitution C A missense_variant W219L 656G>T LICA-CN 11 65365898 65365898 single base substitution C A missense_variant W546L 1637G>T LICA-CN 11 65365898 65365898 single base substitution C A missense_variant W803L 2408G>T LICA-FR 11 65360390 65360390 single base substitution A G downstream_gene_variant LICA-FR 11 65361108 65361134 deletion of <=200bp GGCAGCAGCACAAAGCTGCTGGCCACC - downstream_gene_variant LICA-FR 11 65365905 65365905 single base substitution C T 3_prime_UTR_variant LICA-FR 11 65365905 65365905 single base substitution C T downstream_gene_variant LICA-FR 11 65365905 65365905 single base substitution C T missense_variant A217T 649G>A LICA-FR 11 65365905 65365905 single base substitution C T missense_variant A544T 1630G>A LICA-FR 11 65365905 65365905 single base substitution C T missense_variant A801T 2401G>A LICA-FR 11 65366021 65366021 single base substitution C A 3_prime_UTR_variant LICA-FR 11 65366021 65366021 single base substitution C A downstream_gene_variant LICA-FR 11 65366021 65366021 single base substitution C A missense_variant G178V 533G>T LICA-FR 11 65366021 65366021 single base substitution C A missense_variant G505V 1514G>T LICA-FR 11 65366021 65366021 single base substitution C A missense_variant G762V 2285G>T LICA-FR 11 65371473 65371473 single base substitution A G downstream_gene_variant LICA-FR 11 65371473 65371473 single base substitution A G intron_variant LICA-FR 11 65371489 65371489 single base substitution T C downstream_gene_variant LICA-FR 11 65371489 65371489 single base substitution T C intron_variant LICA-FR 11 65375130 65375130 single base substitution C T downstream_gene_variant LICA-FR 11 65375130 65375130 single base substitution C T exon_variant LICA-FR 11 65375130 65375130 single base substitution C T synonymous_variant E152E 456G>A LICA-FR 11 65375130 65375130 single base substitution C T synonymous_variant E409E 1227G>A LICA-FR 11 65375130 65375130 single base substitution C T upstream_gene_variant LICA-FR 11 65386456 65386456 single base substitution G T upstream_gene_variant LIHC-US 11 65365896 65365896 single base substitution T C 3_prime_UTR_variant LIHC-US 11 65365896 65365896 single base substitution T C downstream_gene_variant LIHC-US 11 65365896 65365896 single base substitution T C missense_variant T220A 658A>G LIHC-US 11 65365896 65365896 single base substitution T C missense_variant T547A 1639A>G LIHC-US 11 65365896 65365896 single base substitution T C missense_variant T804A 2410A>G LIHC-US 11 65380716 65380716 single base substitution A T exon_variant LIHC-US 11 65380716 65380716 single base substitution A T intron_variant LIHC-US 11 65380716 65380716 single base substitution A T missense_variant L171Q 512T>A LIHC-US 11 65380716 65380716 single base substitution A T upstream_gene_variant LINC-JP 11 65360616 65360616 single base substitution C T downstream_gene_variant LINC-JP 11 65366936 65366936 single base substitution A T 3_prime_UTR_variant LINC-JP 11 65366936 65366936 single base substitution A T exon_variant LINC-JP 11 65366936 65366936 single base substitution A T missense_variant L128Q 383T>A LINC-JP 11 65366936 65366936 single base substitution A T missense_variant L455Q 1364T>A LINC-JP 11 65366936 65366936 single base substitution A T missense_variant L712Q 2135T>A LINC-JP 11 65374837 65374837 single base substitution C T downstream_gene_variant LINC-JP 11 65374837 65374837 single base substitution C T exon_variant LINC-JP 11 65374837 65374837 single base substitution C T missense_variant D208N 622G>A LINC-JP 11 65374837 65374837 single base substitution C T missense_variant D465N 1393G>A LINC-JP 11 65374837 65374837 single base substitution C T upstream_gene_variant LINC-JP 11 65380493 65380493 single base substitution G A exon_variant LINC-JP 11 65380493 65380493 single base substitution G A intron_variant LINC-JP 11 65380493 65380493 single base substitution G A synonymous_variant N245N 735C>T LINC-JP 11 65380493 65380493 single base substitution G A upstream_gene_variant LINC-JP 11 65380685 65380685 single base substitution A C exon_variant LINC-JP 11 65380685 65380685 single base substitution A C intron_variant LINC-JP 11 65380685 65380685 single base substitution A C synonymous_variant A181A 543T>G LINC-JP 11 65380685 65380685 single base substitution A C upstream_gene_variant LINC-JP 11 65381684 65381684 single base substitution G C 5_prime_UTR_variant LINC-JP 11 65381684 65381684 single base substitution G C exon_variant LINC-JP 11 65381684 65381684 single base substitution G C upstream_gene_variant LINC-JP 11 65381690 65381690 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 11 65381690 65381690 single base substitution G A exon_variant LINC-JP 11 65381690 65381690 single base substitution G A upstream_gene_variant LINC-JP 11 65383809 65383809 single base substitution G A upstream_gene_variant LINC-JP 11 65385630 65385630 single base substitution C A upstream_gene_variant LIRI-JP 11 65363699 65363699 single base substitution T A downstream_gene_variant LIRI-JP 11 65366620 65366620 single base substitution T C downstream_gene_variant LIRI-JP 11 65366620 65366620 single base substitution T C intron_variant LIRI-JP 11 65366915 65366915 single base substitution G C 3_prime_UTR_variant LIRI-JP 11 65366915 65366915 single base substitution G C downstream_gene_variant LIRI-JP 11 65366915 65366915 single base substitution G C missense_variant P135R 404C>G LIRI-JP 11 65366915 65366915 single base substitution G C missense_variant P462R 1385C>G LIRI-JP 11 65366915 65366915 single base substitution G C missense_variant P719R 2156C>G LIRI-JP 11 65368954 65368954 single base substitution G T downstream_gene_variant LIRI-JP 11 65368954 65368954 single base substitution G T intron_variant LIRI-JP 11 65369009 65369009 single base substitution C T downstream_gene_variant LIRI-JP 11 65369009 65369009 single base substitution C T intron_variant LIRI-JP 11 65369013 65369013 single base substitution G A downstream_gene_variant LIRI-JP 11 65369013 65369013 single base substitution G A intron_variant LIRI-JP 11 65371468 65371468 single base substitution C A downstream_gene_variant LIRI-JP 11 65371468 65371468 single base substitution C A intron_variant LIRI-JP 11 65371900 65371900 single base substitution C T downstream_gene_variant LIRI-JP 11 65371900 65371900 single base substitution C T intron_variant LIRI-JP 11 65379483 65379483 single base substitution G T exon_variant LIRI-JP 11 65379483 65379483 single base substitution G T intron_variant LIRI-JP 11 65379483 65379483 single base substitution G T upstream_gene_variant LIRI-JP 11 65380534 65380534 single base substitution C A exon_variant LIRI-JP 11 65380534 65380534 single base substitution C A intron_variant LIRI-JP 11 65380534 65380534 single base substitution C A stop_gained E232* 694G>T LIRI-JP 11 65380534 65380534 single base substitution C A upstream_gene_variant LIRI-JP 11 65386187 65386187 single base substitution T C upstream_gene_variant LIRI-JP 11 65386211 65386211 single base substitution G A upstream_gene_variant LUSC-KR 11 65363399 65363399 single base substitution T G downstream_gene_variant LUSC-KR 11 65365958 65365958 single base substitution G T 3_prime_UTR_variant LUSC-KR 11 65365958 65365958 single base substitution G T downstream_gene_variant LUSC-KR 11 65365958 65365958 single base substitution G T stop_gained S199* 596C>A LUSC-KR 11 65365958 65365958 single base substitution G T stop_gained S526* 1577C>A LUSC-KR 11 65365958 65365958 single base substitution G T stop_gained S783* 2348C>A LUSC-KR 11 65376676 65376676 single base substitution C G exon_variant LUSC-KR 11 65376676 65376676 single base substitution C G intron_variant LUSC-KR 11 65376676 65376676 single base substitution C G upstream_gene_variant LUSC-KR 11 65382937 65382937 single base substitution G A upstream_gene_variant LUSC-KR 11 65387012 65387012 single base substitution C T upstream_gene_variant LUSC-US 11 65360632 65360632 single base substitution G A downstream_gene_variant LUSC-US 11 65373256 65373256 single base substitution G A 3_prime_UTR_variant LUSC-US 11 65373256 65373256 single base substitution G A downstream_gene_variant LUSC-US 11 65373256 65373256 single base substitution G A exon_variant LUSC-US 11 65373256 65373256 single base substitution G A missense_variant P19S 55C>T LUSC-US 11 65373256 65373256 single base substitution G A missense_variant P346S 1036C>T LUSC-US 11 65373256 65373256 single base substitution G A missense_variant P603S 1807C>T LUSC-US 11 65375242 65375242 single base substitution A G downstream_gene_variant LUSC-US 11 65375242 65375242 single base substitution A G exon_variant LUSC-US 11 65375242 65375242 single base substitution A G intron_variant LUSC-US 11 65375242 65375242 single base substitution A G missense_variant I115T 344T>C LUSC-US 11 65375242 65375242 single base substitution A G missense_variant I372T 1115T>C LUSC-US 11 65375242 65375242 single base substitution A G upstream_gene_variant LUSC-US 11 65375870 65375870 single base substitution C T downstream_gene_variant LUSC-US 11 65375870 65375870 single base substitution C T exon_variant LUSC-US 11 65375870 65375870 single base substitution C T synonymous_variant L13L 39G>A LUSC-US 11 65375870 65375870 single base substitution C T synonymous_variant L263L 789G>A LUSC-US 11 65375870 65375870 single base substitution C T synonymous_variant L6L 18G>A LUSC-US 11 65375870 65375870 single base substitution C T upstream_gene_variant LUSC-US 11 65384478 65384478 single base substitution C A upstream_gene_variant LUSC-US 11 65385808 65385808 single base substitution C T upstream_gene_variant MALY-DE 11 65378665 65378665 single base substitution G T 5_prime_UTR_variant MALY-DE 11 65378665 65378665 single base substitution G T exon_variant MALY-DE 11 65378665 65378665 single base substitution G T intron_variant MALY-DE 11 65378665 65378665 single base substitution G T upstream_gene_variant MALY-DE 11 65382186 65382186 single base substitution T G exon_variant MALY-DE 11 65382186 65382186 single base substitution T G upstream_gene_variant MALY-DE 11 65385248 65385248 single base substitution T C upstream_gene_variant MELA-AU 11 65361542 65361542 single base substitution G A downstream_gene_variant MELA-AU 11 65362932 65362933 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 65362965 65362965 single base substitution G A downstream_gene_variant MELA-AU 11 65363186 65363186 single base substitution C T downstream_gene_variant MELA-AU 11 65363280 65363280 single base substitution C T downstream_gene_variant MELA-AU 11 65363390 65363390 single base substitution G A downstream_gene_variant MELA-AU 11 65363638 65363638 single base substitution C T downstream_gene_variant MELA-AU 11 65363653 65363653 single base substitution G A downstream_gene_variant MELA-AU 11 65363680 65363680 single base substitution A G downstream_gene_variant MELA-AU 11 65363886 65363886 single base substitution G A downstream_gene_variant MELA-AU 11 65364219 65364219 single base substitution A C downstream_gene_variant MELA-AU 11 65364402 65364402 single base substitution C T downstream_gene_variant MELA-AU 11 65364692 65364692 single base substitution T C downstream_gene_variant MELA-AU 11 65364718 65364718 single base substitution G A downstream_gene_variant MELA-AU 11 65365995 65365995 single base substitution G T 3_prime_UTR_variant MELA-AU 11 65365995 65365995 single base substitution G T downstream_gene_variant MELA-AU 11 65365995 65365995 single base substitution G T missense_variant P187T 559C>A MELA-AU 11 65365995 65365995 single base substitution G T missense_variant P514T 1540C>A MELA-AU 11 65365995 65365995 single base substitution G T missense_variant P771T 2311C>A MELA-AU 11 65367011 65367011 single base substitution G A 3_prime_UTR_variant MELA-AU 11 65367011 65367011 single base substitution G A exon_variant MELA-AU 11 65367011 65367011 single base substitution G A missense_variant P103L 308C>T MELA-AU 11 65367011 65367011 single base substitution G A missense_variant P430L 1289C>T MELA-AU 11 65367011 65367011 single base substitution G A missense_variant P687L 2060C>T MELA-AU 11 65367360 65367360 single base substitution G A intron_variant MELA-AU 11 65368102 65368102 single base substitution G A intron_variant MELA-AU 11 65368811 65368811 single base substitution A G downstream_gene_variant MELA-AU 11 65368811 65368811 single base substitution A G intron_variant MELA-AU 11 65370044 65370044 single base substitution G A downstream_gene_variant MELA-AU 11 65370044 65370044 single base substitution G A intron_variant MELA-AU 11 65370598 65370598 single base substitution G A downstream_gene_variant MELA-AU 11 65370598 65370598 single base substitution G A intron_variant MELA-AU 11 65370778 65370779 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 65370778 65370779 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 65371126 65371126 single base substitution A C downstream_gene_variant MELA-AU 11 65371126 65371126 single base substitution A C intron_variant MELA-AU 11 65371698 65371698 single base substitution G A downstream_gene_variant MELA-AU 11 65371698 65371698 single base substitution G A intron_variant MELA-AU 11 65372960 65372960 single base substitution G A downstream_gene_variant MELA-AU 11 65372960 65372960 single base substitution G A intron_variant MELA-AU 11 65373123 65373123 single base substitution G A downstream_gene_variant MELA-AU 11 65373123 65373123 single base substitution G A intron_variant MELA-AU 11 65373513 65373513 single base substitution G A 3_prime_UTR_variant MELA-AU 11 65373513 65373513 single base substitution G A 5_prime_UTR_variant MELA-AU 11 65373513 65373513 single base substitution G A downstream_gene_variant MELA-AU 11 65373513 65373513 single base substitution G A exon_variant MELA-AU 11 65373513 65373513 single base substitution G A missense_variant S291F 872C>T MELA-AU 11 65373513 65373513 single base substitution G A missense_variant S548F 1643C>T MELA-AU 11 65373722 65373722 single base substitution G A downstream_gene_variant MELA-AU 11 65373722 65373722 single base substitution G A exon_variant MELA-AU 11 65373722 65373722 single base substitution G A intron_variant MELA-AU 11 65374044 65374044 single base substitution G A downstream_gene_variant MELA-AU 11 65374044 65374044 single base substitution G A exon_variant MELA-AU 11 65374044 65374044 single base substitution G A intron_variant MELA-AU 11 65374044 65374044 single base substitution G A upstream_gene_variant MELA-AU 11 65374294 65374294 single base substitution G A 5_prime_UTR_variant MELA-AU 11 65374294 65374294 single base substitution G A downstream_gene_variant MELA-AU 11 65374294 65374294 single base substitution G A intron_variant MELA-AU 11 65374294 65374294 single base substitution G A upstream_gene_variant MELA-AU 11 65375409 65375409 single base substitution G A downstream_gene_variant MELA-AU 11 65375409 65375409 single base substitution G A exon_variant MELA-AU 11 65375409 65375409 single base substitution G A synonymous_variant F101F 303C>T MELA-AU 11 65375409 65375409 single base substitution G A synonymous_variant F351F 1053C>T MELA-AU 11 65375409 65375409 single base substitution G A synonymous_variant F94F 282C>T MELA-AU 11 65375409 65375409 single base substitution G A upstream_gene_variant MELA-AU 11 65376632 65376632 single base substitution G A exon_variant MELA-AU 11 65376632 65376632 single base substitution G A intron_variant MELA-AU 11 65376632 65376632 single base substitution G A upstream_gene_variant MELA-AU 11 65376912 65376912 single base substitution G A exon_variant MELA-AU 11 65376912 65376912 single base substitution G A intron_variant MELA-AU 11 65376912 65376912 single base substitution G A upstream_gene_variant MELA-AU 11 65378316 65378316 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 65378316 65378316 single base substitution T A exon_variant MELA-AU 11 65378316 65378316 single base substitution T A intron_variant MELA-AU 11 65378316 65378316 single base substitution T A upstream_gene_variant MELA-AU 11 65378824 65378824 single base substitution A G exon_variant MELA-AU 11 65378824 65378824 single base substitution A G intron_variant MELA-AU 11 65378824 65378824 single base substitution A G upstream_gene_variant MELA-AU 11 65378910 65378910 single base substitution G A exon_variant MELA-AU 11 65378910 65378910 single base substitution G A intron_variant MELA-AU 11 65378910 65378910 single base substitution G A upstream_gene_variant MELA-AU 11 65379018 65379018 single base substitution G A exon_variant MELA-AU 11 65379018 65379018 single base substitution G A intron_variant MELA-AU 11 65379018 65379018 single base substitution G A upstream_gene_variant MELA-AU 11 65379050 65379050 single base substitution C T exon_variant MELA-AU 11 65379050 65379050 single base substitution C T intron_variant MELA-AU 11 65379050 65379050 single base substitution C T upstream_gene_variant MELA-AU 11 65379209 65379209 insertion of <=200bp - T exon_variant MELA-AU 11 65379209 65379209 insertion of <=200bp - T intron_variant MELA-AU 11 65379209 65379209 insertion of <=200bp - T upstream_gene_variant MELA-AU 11 65380157 65380157 single base substitution G A exon_variant MELA-AU 11 65380157 65380157 single base substitution G A intron_variant MELA-AU 11 65380157 65380157 single base substitution G A upstream_gene_variant MELA-AU 11 65380435 65380435 single base substitution G A exon_variant MELA-AU 11 65380435 65380435 single base substitution G A intron_variant MELA-AU 11 65380435 65380435 single base substitution G A upstream_gene_variant MELA-AU 11 65380553 65380553 single base substitution C T exon_variant MELA-AU 11 65380553 65380553 single base substitution C T intron_variant MELA-AU 11 65380553 65380553 single base substitution C T synonymous_variant G225G 675G>A MELA-AU 11 65380553 65380553 single base substitution C T upstream_gene_variant MELA-AU 11 65382848 65382848 single base substitution G A exon_variant MELA-AU 11 65382848 65382848 single base substitution G A upstream_gene_variant MELA-AU 11 65382853 65382853 single base substitution C T exon_variant MELA-AU 11 65382853 65382853 single base substitution C T upstream_gene_variant MELA-AU 11 65382896 65382896 single base substitution G A upstream_gene_variant MELA-AU 11 65382940 65382940 single base substitution G A upstream_gene_variant MELA-AU 11 65382942 65382942 single base substitution G A upstream_gene_variant MELA-AU 11 65383036 65383036 single base substitution C T upstream_gene_variant MELA-AU 11 65383221 65383221 single base substitution C T upstream_gene_variant MELA-AU 11 65383222 65383222 single base substitution C T upstream_gene_variant MELA-AU 11 65383647 65383648 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 65384686 65384686 single base substitution G A upstream_gene_variant MELA-AU 11 65384895 65384895 single base substitution C T upstream_gene_variant MELA-AU 11 65385193 65385193 single base substitution G A upstream_gene_variant MELA-AU 11 65385226 65385226 single base substitution C T upstream_gene_variant MELA-AU 11 65385397 65385397 single base substitution C T upstream_gene_variant MELA-AU 11 65385419 65385419 single base substitution C T upstream_gene_variant MELA-AU 11 65385488 65385489 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 65385677 65385677 single base substitution C T upstream_gene_variant MELA-AU 11 65385853 65385853 single base substitution C T upstream_gene_variant MELA-AU 11 65385938 65385938 single base substitution G A upstream_gene_variant MELA-AU 11 65386041 65386041 single base substitution C T upstream_gene_variant MELA-AU 11 65386229 65386229 single base substitution C T upstream_gene_variant MELA-AU 11 65387173 65387173 single base substitution G T upstream_gene_variant ORCA-IN 11 65361309 65361309 deletion of <=200bp T - downstream_gene_variant ORCA-IN 11 65364533 65364533 single base substitution C T downstream_gene_variant ORCA-IN 11 65366128 65366128 single base substitution C T downstream_gene_variant ORCA-IN 11 65366128 65366128 single base substitution C T intron_variant OV-AU 11 65360259 65360259 single base substitution G C downstream_gene_variant OV-AU 11 65366036 65366036 single base substitution C T 3_prime_UTR_variant OV-AU 11 65366036 65366036 single base substitution C T downstream_gene_variant OV-AU 11 65366036 65366036 single base substitution C T missense_variant R173H 518G>A OV-AU 11 65366036 65366036 single base substitution C T missense_variant R500H 1499G>A OV-AU 11 65366036 65366036 single base substitution C T missense_variant R757H 2270G>A OV-AU 11 65366825 65366825 single base substitution G A downstream_gene_variant OV-AU 11 65366825 65366825 single base substitution G A intron_variant OV-AU 11 65367140 65367140 single base substitution G A 3_prime_UTR_variant OV-AU 11 65367140 65367140 single base substitution G A exon_variant OV-AU 11 65367140 65367140 single base substitution G A missense_variant A387V 1160C>T OV-AU 11 65367140 65367140 single base substitution G A missense_variant A60V 179C>T OV-AU 11 65367140 65367140 single base substitution G A missense_variant A644V 1931C>T OV-AU 11 65368672 65368672 single base substitution T G downstream_gene_variant OV-AU 11 65368672 65368672 single base substitution T G intron_variant OV-AU 11 65375224 65375224 single base substitution G A downstream_gene_variant OV-AU 11 65375224 65375224 single base substitution G A exon_variant OV-AU 11 65375224 65375224 single base substitution G A intron_variant OV-AU 11 65375224 65375224 single base substitution G A missense_variant A121V 362C>T OV-AU 11 65375224 65375224 single base substitution G A missense_variant A378V 1133C>T OV-AU 11 65375224 65375224 single base substitution G A upstream_gene_variant OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - downstream_gene_variant OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - exon_variant OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - frameshift_variant I247 OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - intron_variant OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - splice_acceptor_variant OV-AU 11 65375919 65375935 deletion of <=200bp ACTAGAGAAGAGGGGCC - upstream_gene_variant OV-AU 11 65376828 65376828 single base substitution G A exon_variant OV-AU 11 65376828 65376828 single base substitution G A intron_variant OV-AU 11 65376828 65376828 single base substitution G A upstream_gene_variant OV-AU 11 65380904 65380904 single base substitution G C exon_variant OV-AU 11 65380904 65380904 single base substitution G C intron_variant OV-AU 11 65380904 65380904 single base substitution G C synonymous_variant P108P 324C>G OV-AU 11 65380904 65380904 single base substitution G C upstream_gene_variant OV-AU 11 65385099 65385099 single base substitution C T upstream_gene_variant PACA-AU 11 65367615 65367615 single base substitution C T intron_variant PACA-AU 11 65376338 65376338 single base substitution C T exon_variant PACA-AU 11 65376338 65376338 single base substitution C T intron_variant PACA-AU 11 65376338 65376338 single base substitution C T upstream_gene_variant PACA-AU 11 65376381 65376381 single base substitution G A exon_variant PACA-AU 11 65376381 65376381 single base substitution G A intron_variant PACA-AU 11 65376381 65376381 single base substitution G A upstream_gene_variant PACA-AU 11 65379099 65379099 single base substitution C T exon_variant PACA-AU 11 65379099 65379099 single base substitution C T intron_variant PACA-AU 11 65379099 65379099 single base substitution C T upstream_gene_variant PACA-AU 11 65381752 65381752 single base substitution G C exon_variant PACA-AU 11 65381752 65381752 single base substitution G C upstream_gene_variant PACA-AU 11 65385027 65385027 single base substitution G T upstream_gene_variant PACA-AU 11 65385028 65385028 single base substitution G T upstream_gene_variant PACA-AU 11 65385272 65385272 single base substitution T C upstream_gene_variant PACA-CA 11 65361560 65361560 single base substitution G T downstream_gene_variant PACA-CA 11 65363902 65363902 single base substitution G T downstream_gene_variant PACA-CA 11 65364465 65364465 insertion of <=200bp - T downstream_gene_variant PACA-CA 11 65365673 65365673 single base substitution C T 3_prime_UTR_variant PACA-CA 11 65365673 65365673 single base substitution C T downstream_gene_variant PACA-CA 11 65366794 65366794 single base substitution A C downstream_gene_variant PACA-CA 11 65366794 65366794 single base substitution A C intron_variant PACA-CA 11 65367704 65367704 single base substitution T G intron_variant PACA-CA 11 65367947 65367947 single base substitution C T intron_variant PACA-CA 11 65370056 65370056 single base substitution G A downstream_gene_variant PACA-CA 11 65370056 65370056 single base substitution G A intron_variant PACA-CA 11 65373123 65373123 single base substitution G C downstream_gene_variant PACA-CA 11 65373123 65373123 single base substitution G C intron_variant PACA-CA 11 65374179 65374179 single base substitution C G 3_prime_UTR_variant PACA-CA 11 65374179 65374179 single base substitution C G 5_prime_UTR_variant PACA-CA 11 65374179 65374179 single base substitution C G downstream_gene_variant PACA-CA 11 65374179 65374179 single base substitution C G exon_variant PACA-CA 11 65374179 65374179 single base substitution C G missense_variant R272P 815G>C PACA-CA 11 65374179 65374179 single base substitution C G missense_variant R529P 1586G>C PACA-CA 11 65374179 65374179 single base substitution C G upstream_gene_variant PACA-CA 11 65377887 65377887 single base substitution C T exon_variant PACA-CA 11 65377887 65377887 single base substitution C T intron_variant PACA-CA 11 65377887 65377887 single base substitution C T upstream_gene_variant PACA-CA 11 65381100 65381100 single base substitution T C exon_variant PACA-CA 11 65381100 65381100 single base substitution T C intron_variant PACA-CA 11 65381100 65381100 single base substitution T C missense_variant N43S 128A>G PACA-CA 11 65381100 65381100 single base substitution T C upstream_gene_variant PACA-CA 11 65381777 65381777 single base substitution C T exon_variant PACA-CA 11 65381777 65381777 single base substitution C T upstream_gene_variant PACA-CA 11 65382704 65382704 single base substitution G A exon_variant PACA-CA 11 65382704 65382704 single base substitution G A upstream_gene_variant PACA-CA 11 65386633 65386633 single base substitution G C upstream_gene_variant PBCA-DE 11 65361038 65361038 single base substitution C T downstream_gene_variant PBCA-DE 11 65364639 65364639 single base substitution A T downstream_gene_variant PBCA-DE 11 65364640 65364640 insertion of <=200bp - T downstream_gene_variant PBCA-DE 11 65374730 65374730 single base substitution C A downstream_gene_variant PBCA-DE 11 65374730 65374730 single base substitution C A exon_variant PBCA-DE 11 65374730 65374730 single base substitution C A intron_variant PBCA-DE 11 65374730 65374730 single base substitution C A upstream_gene_variant PBCA-DE 11 65382893 65382893 single base substitution C A upstream_gene_variant PBCA-DE 11 65386397 65386397 single base substitution A G upstream_gene_variant PRAD-CA 11 65364306 65364306 single base substitution T A downstream_gene_variant PRAD-UK 11 65368727 65368727 single base substitution T C downstream_gene_variant PRAD-UK 11 65368727 65368727 single base substitution T C intron_variant PRAD-UK 11 65374804 65374804 single base substitution C T downstream_gene_variant PRAD-UK 11 65374804 65374804 single base substitution C T exon_variant PRAD-UK 11 65374804 65374804 single base substitution C T missense_variant G219R 655G>A PRAD-UK 11 65374804 65374804 single base substitution C T missense_variant G476R 1426G>A PRAD-UK 11 65374804 65374804 single base substitution C T upstream_gene_variant PRAD-UK 11 65378535 65378535 single base substitution G T 5_prime_UTR_variant PRAD-UK 11 65378535 65378535 single base substitution G T exon_variant PRAD-UK 11 65378535 65378535 single base substitution G T intron_variant PRAD-UK 11 65378535 65378535 single base substitution G T upstream_gene_variant PRAD-US 11 65365835 65365835 deletion of <=200bp C - 3_prime_UTR_variant PRAD-US 11 65365835 65365835 deletion of <=200bp C - downstream_gene_variant PRAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G240 PRAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G567 PRAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G824 PRAD-US 11 65366866 65366866 single base substitution G A downstream_gene_variant PRAD-US 11 65366866 65366866 single base substitution G A splice_region_variant PRAD-US 11 65375265 65375265 single base substitution G A downstream_gene_variant PRAD-US 11 65375265 65375265 single base substitution G A exon_variant PRAD-US 11 65375265 65375265 single base substitution G A intron_variant PRAD-US 11 65375265 65375265 single base substitution G A synonymous_variant H107H 321C>T PRAD-US 11 65375265 65375265 single base substitution G A synonymous_variant H364H 1092C>T PRAD-US 11 65375265 65375265 single base substitution G A upstream_gene_variant READ-US 11 65375494 65375494 single base substitution C T downstream_gene_variant READ-US 11 65375494 65375494 single base substitution C T exon_variant READ-US 11 65375494 65375494 single base substitution C T missense_variant R323H 968G>A READ-US 11 65375494 65375494 single base substitution C T missense_variant R66H 197G>A READ-US 11 65375494 65375494 single base substitution C T missense_variant R73H 218G>A READ-US 11 65375494 65375494 single base substitution C T upstream_gene_variant READ-US 11 65380783 65380783 single base substitution C T exon_variant READ-US 11 65380783 65380783 single base substitution C T intron_variant READ-US 11 65380783 65380783 single base substitution C T missense_variant D149N 445G>A READ-US 11 65380783 65380783 single base substitution C T upstream_gene_variant READ-US 11 65386302 65386302 single base substitution G A upstream_gene_variant RECA-EU 11 65361906 65361906 single base substitution C T downstream_gene_variant RECA-EU 11 65371516 65371516 single base substitution G A downstream_gene_variant RECA-EU 11 65371516 65371516 single base substitution G A intron_variant SKCA-BR 11 65363459 65363459 single base substitution G A downstream_gene_variant SKCA-BR 11 65363865 65363865 single base substitution A G downstream_gene_variant SKCA-BR 11 65364339 65364339 single base substitution G A downstream_gene_variant SKCA-BR 11 65364348 65364348 single base substitution T A downstream_gene_variant SKCA-BR 11 65365846 65365846 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 65365846 65365846 single base substitution G A downstream_gene_variant SKCA-BR 11 65365846 65365846 single base substitution G A synonymous_variant P236P 708C>T SKCA-BR 11 65365846 65365846 single base substitution G A synonymous_variant P563P 1689C>T SKCA-BR 11 65365846 65365846 single base substitution G A synonymous_variant P820P 2460C>T SKCA-BR 11 65366240 65366240 single base substitution T C downstream_gene_variant SKCA-BR 11 65366240 65366240 single base substitution T C intron_variant SKCA-BR 11 65369673 65369674 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 11 65369673 65369674 deletion of <=200bp CA - intron_variant SKCA-BR 11 65372197 65372204 deletion of <=200bp CTGGGTGG - downstream_gene_variant SKCA-BR 11 65372197 65372204 deletion of <=200bp CTGGGTGG - intron_variant SKCA-BR 11 65374138 65374138 single base substitution G A downstream_gene_variant SKCA-BR 11 65374138 65374138 single base substitution G A exon_variant SKCA-BR 11 65374138 65374138 single base substitution G A intron_variant SKCA-BR 11 65374138 65374138 single base substitution G A upstream_gene_variant SKCA-BR 11 65375265 65375265 single base substitution G A downstream_gene_variant SKCA-BR 11 65375265 65375265 single base substitution G A exon_variant SKCA-BR 11 65375265 65375265 single base substitution G A intron_variant SKCA-BR 11 65375265 65375265 single base substitution G A synonymous_variant H107H 321C>T SKCA-BR 11 65375265 65375265 single base substitution G A synonymous_variant H364H 1092C>T SKCA-BR 11 65375265 65375265 single base substitution G A upstream_gene_variant SKCA-BR 11 65382159 65382159 single base substitution C T exon_variant SKCA-BR 11 65382159 65382159 single base substitution C T upstream_gene_variant SKCA-BR 11 65383545 65383545 single base substitution A C upstream_gene_variant SKCA-BR 11 65385254 65385254 single base substitution C T upstream_gene_variant SKCA-BR 11 65385826 65385826 single base substitution C T upstream_gene_variant SKCM-US 11 65363008 65363008 single base substitution G A downstream_gene_variant SKCM-US 11 65366005 65366005 single base substitution A T 3_prime_UTR_variant SKCM-US 11 65366005 65366005 single base substitution A T downstream_gene_variant SKCM-US 11 65366005 65366005 single base substitution A T synonymous_variant P183P 549T>A SKCM-US 11 65366005 65366005 single base substitution A T synonymous_variant P510P 1530T>A SKCM-US 11 65366005 65366005 single base substitution A T synonymous_variant P767P 2301T>A SKCM-US 11 65366868 65366868 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65366868 65366868 single base substitution G A downstream_gene_variant SKCM-US 11 65366868 65366868 single base substitution G A missense_variant R151C 451C>T SKCM-US 11 65366868 65366868 single base substitution G A missense_variant R478C 1432C>T SKCM-US 11 65366868 65366868 single base substitution G A missense_variant R735C 2203C>T SKCM-US 11 65366992 65366992 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65366992 65366992 single base substitution G A exon_variant SKCM-US 11 65366992 65366992 single base substitution G A synonymous_variant S109S 327C>T SKCM-US 11 65366992 65366992 single base substitution G A synonymous_variant S436S 1308C>T SKCM-US 11 65366992 65366992 single base substitution G A synonymous_variant S693S 2079C>T SKCM-US 11 65367008 65367008 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65367008 65367008 single base substitution G A exon_variant SKCM-US 11 65367008 65367008 single base substitution G A missense_variant T104I 311C>T SKCM-US 11 65367008 65367008 single base substitution G A missense_variant T431I 1292C>T SKCM-US 11 65367008 65367008 single base substitution G A missense_variant T688I 2063C>T SKCM-US 11 65367011 65367011 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65367011 65367011 single base substitution G A exon_variant SKCM-US 11 65367011 65367011 single base substitution G A missense_variant P103L 308C>T SKCM-US 11 65367011 65367011 single base substitution G A missense_variant P430L 1289C>T SKCM-US 11 65367011 65367011 single base substitution G A missense_variant P687L 2060C>T SKCM-US 11 65373427 65373427 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65373427 65373427 single base substitution G A 5_prime_UTR_variant SKCM-US 11 65373427 65373427 single base substitution G A downstream_gene_variant SKCM-US 11 65373427 65373427 single base substitution G A exon_variant SKCM-US 11 65373427 65373427 single base substitution G A stop_gained Q320* 958C>T SKCM-US 11 65373427 65373427 single base substitution G A stop_gained Q577* 1729C>T SKCM-US 11 65373447 65373447 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65373447 65373447 single base substitution G A 5_prime_UTR_variant SKCM-US 11 65373447 65373447 single base substitution G A downstream_gene_variant SKCM-US 11 65373447 65373447 single base substitution G A exon_variant SKCM-US 11 65373447 65373447 single base substitution G A missense_variant S313F 938C>T SKCM-US 11 65373447 65373447 single base substitution G A missense_variant S570F 1709C>T SKCM-US 11 65373509 65373509 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65373509 65373509 single base substitution G A 5_prime_UTR_variant SKCM-US 11 65373509 65373509 single base substitution G A downstream_gene_variant SKCM-US 11 65373509 65373509 single base substitution G A exon_variant SKCM-US 11 65373509 65373509 single base substitution G A synonymous_variant P292P 876C>T SKCM-US 11 65373509 65373509 single base substitution G A synonymous_variant P549P 1647C>T SKCM-US 11 65374967 65374967 single base substitution C T downstream_gene_variant SKCM-US 11 65374967 65374967 single base substitution C T exon_variant SKCM-US 11 65374967 65374967 single base substitution C T synonymous_variant E164E 492G>A SKCM-US 11 65374967 65374967 single base substitution C T synonymous_variant E421E 1263G>A SKCM-US 11 65374967 65374967 single base substitution C T upstream_gene_variant SKCM-US 11 65375207 65375207 single base substitution G A downstream_gene_variant SKCM-US 11 65375207 65375207 single base substitution G A exon_variant SKCM-US 11 65375207 65375207 single base substitution G A intron_variant SKCM-US 11 65375207 65375207 single base substitution G A synonymous_variant L127L 379C>T SKCM-US 11 65375207 65375207 single base substitution G A synonymous_variant L384L 1150C>T SKCM-US 11 65375207 65375207 single base substitution G A upstream_gene_variant SKCM-US 11 65375744 65375744 single base substitution G A downstream_gene_variant SKCM-US 11 65375744 65375744 single base substitution G A exon_variant SKCM-US 11 65375744 65375744 single base substitution G A synonymous_variant V305V 915C>T SKCM-US 11 65375744 65375744 single base substitution G A synonymous_variant V48V 144C>T SKCM-US 11 65375744 65375744 single base substitution G A synonymous_variant V55V 165C>T SKCM-US 11 65375744 65375744 single base substitution G A upstream_gene_variant SKCM-US 11 65380868 65380868 single base substitution C T exon_variant SKCM-US 11 65380868 65380868 single base substitution C T intron_variant SKCM-US 11 65380868 65380868 single base substitution C T synonymous_variant E120E 360G>A SKCM-US 11 65380868 65380868 single base substitution C T upstream_gene_variant SKCM-US 11 65385893 65385893 single base substitution C T upstream_gene_variant SKCM-US 11 65385973 65385973 single base substitution C T upstream_gene_variant SKCM-US 11 65386194 65386194 single base substitution C T upstream_gene_variant SKCM-US 11 65386245 65386245 single base substitution C T upstream_gene_variant STAD-US 11 65360486 65360486 deletion of <=200bp G - downstream_gene_variant STAD-US 11 65360996 65360996 single base substitution G A downstream_gene_variant STAD-US 11 65360998 65360998 single base substitution C T downstream_gene_variant STAD-US 11 65361001 65361001 single base substitution G A downstream_gene_variant STAD-US 11 65361010 65361010 single base substitution G A downstream_gene_variant STAD-US 11 65365835 65365835 deletion of <=200bp C - 3_prime_UTR_variant STAD-US 11 65365835 65365835 deletion of <=200bp C - downstream_gene_variant STAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G240 STAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G567 STAD-US 11 65365835 65365835 deletion of <=200bp C - frameshift_variant G824 STAD-US 11 65365879 65365879 single base substitution T G 3_prime_UTR_variant STAD-US 11 65365879 65365879 single base substitution T G downstream_gene_variant STAD-US 11 65365879 65365879 single base substitution T G synonymous_variant S225S 675A>C STAD-US 11 65365879 65365879 single base substitution T G synonymous_variant S552S 1656A>C STAD-US 11 65365879 65365879 single base substitution T G synonymous_variant S809S 2427A>C STAD-US 11 65365885 65365885 single base substitution C T 3_prime_UTR_variant STAD-US 11 65365885 65365885 single base substitution C T downstream_gene_variant STAD-US 11 65365885 65365885 single base substitution C T synonymous_variant P223P 669G>A STAD-US 11 65365885 65365885 single base substitution C T synonymous_variant P550P 1650G>A STAD-US 11 65365885 65365885 single base substitution C T synonymous_variant P807P 2421G>A STAD-US 11 65366996 65366996 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 11 65366996 65366996 deletion of <=200bp G - exon_variant STAD-US 11 65366996 65366996 deletion of <=200bp G - frameshift_variant P108 STAD-US 11 65366996 65366996 deletion of <=200bp G - frameshift_variant P435 STAD-US 11 65366996 65366996 deletion of <=200bp G - frameshift_variant P692 STAD-US 11 65367021 65367021 single base substitution C T 3_prime_UTR_variant STAD-US 11 65367021 65367021 single base substitution C T exon_variant STAD-US 11 65367021 65367021 single base substitution C T missense_variant A100T 298G>A STAD-US 11 65367021 65367021 single base substitution C T missense_variant A427T 1279G>A STAD-US 11 65367021 65367021 single base substitution C T missense_variant A684T 2050G>A STAD-US 11 65367065 65367065 single base substitution C T 3_prime_UTR_variant STAD-US 11 65367065 65367065 single base substitution C T exon_variant STAD-US 11 65367065 65367065 single base substitution C T missense_variant R412H 1235G>A STAD-US 11 65367065 65367065 single base substitution C T missense_variant R669H 2006G>A STAD-US 11 65367065 65367065 single base substitution C T missense_variant R85H 254G>A STAD-US 11 65374207 65374207 single base substitution C T 3_prime_UTR_variant STAD-US 11 65374207 65374207 single base substitution C T 5_prime_UTR_variant STAD-US 11 65374207 65374207 single base substitution C T downstream_gene_variant STAD-US 11 65374207 65374207 single base substitution C T exon_variant STAD-US 11 65374207 65374207 single base substitution C T missense_variant G263R 787G>A STAD-US 11 65374207 65374207 single base substitution C T missense_variant G520R 1558G>A STAD-US 11 65374207 65374207 single base substitution C T upstream_gene_variant STAD-US 11 65374866 65374866 single base substitution C T downstream_gene_variant STAD-US 11 65374866 65374866 single base substitution C T exon_variant STAD-US 11 65374866 65374866 single base substitution C T missense_variant R198H 593G>A STAD-US 11 65374866 65374866 single base substitution C T missense_variant R455H 1364G>A STAD-US 11 65374866 65374866 single base substitution C T upstream_gene_variant STAD-US 11 65375465 65375465 single base substitution C T downstream_gene_variant STAD-US 11 65375465 65375465 single base substitution C T exon_variant STAD-US 11 65375465 65375465 single base substitution C T missense_variant G333S 997G>A STAD-US 11 65375465 65375465 single base substitution C T missense_variant G76S 226G>A STAD-US 11 65375465 65375465 single base substitution C T missense_variant G83S 247G>A STAD-US 11 65375465 65375465 single base substitution C T upstream_gene_variant STAD-US 11 65375502 65375502 single base substitution C T downstream_gene_variant STAD-US 11 65375502 65375502 single base substitution C T exon_variant STAD-US 11 65375502 65375502 single base substitution C T synonymous_variant V320V 960G>A STAD-US 11 65375502 65375502 single base substitution C T synonymous_variant V63V 189G>A STAD-US 11 65375502 65375502 single base substitution C T synonymous_variant V70V 210G>A STAD-US 11 65375502 65375502 single base substitution C T upstream_gene_variant STAD-US 11 65375538 65375538 deletion of <=200bp A - downstream_gene_variant STAD-US 11 65375538 65375538 deletion of <=200bp A - exon_variant STAD-US 11 65375538 65375538 deletion of <=200bp A - frameshift_variant F308 STAD-US 11 65375538 65375538 deletion of <=200bp A - frameshift_variant F51 STAD-US 11 65375538 65375538 deletion of <=200bp A - frameshift_variant F58 STAD-US 11 65375538 65375538 deletion of <=200bp A - upstream_gene_variant STAD-US 11 65375801 65375801 single base substitution G A downstream_gene_variant STAD-US 11 65375801 65375801 single base substitution G A exon_variant STAD-US 11 65375801 65375801 single base substitution G A synonymous_variant Y286Y 858C>T STAD-US 11 65375801 65375801 single base substitution G A synonymous_variant Y29Y 87C>T STAD-US 11 65375801 65375801 single base substitution G A synonymous_variant Y36Y 108C>T STAD-US 11 65375801 65375801 single base substitution G A upstream_gene_variant STAD-US 11 65380788 65380788 single base substitution C T exon_variant STAD-US 11 65380788 65380788 single base substitution C T intron_variant STAD-US 11 65380788 65380788 single base substitution C T missense_variant R147H 440G>A STAD-US 11 65380788 65380788 single base substitution C T upstream_gene_variant STAD-US 11 65380977 65380977 single base substitution C A exon_variant STAD-US 11 65380977 65380977 single base substitution C A intron_variant STAD-US 11 65380977 65380977 single base substitution C A missense_variant W84L 251G>T STAD-US 11 65380977 65380977 single base substitution C A upstream_gene_variant STAD-US 11 65385537 65385537 single base substitution C T upstream_gene_variant STAD-US 11 65385540 65385540 single base substitution C A upstream_gene_variant STAD-US 11 65385650 65385650 single base substitution C T upstream_gene_variant STAD-US 11 65386029 65386029 single base substitution G A upstream_gene_variant STAD-US 11 65386142 65386142 single base substitution C T upstream_gene_variant STAD-US 11 65386239 65386239 deletion of <=200bp G - upstream_gene_variant STAD-US 11 65386337 65386337 single base substitution C T upstream_gene_variant STAD-US 11 65387008 65387008 single base substitution C T upstream_gene_variant STAD-US 11 65387251 65387251 single base substitution G A upstream_gene_variant STAD-US 11 65387389 65387389 single base substitution T G upstream_gene_variant THCA-SA 11 65361256 65361256 single base substitution C T downstream_gene_variant THCA-SA 11 65363275 65363275 single base substitution G A downstream_gene_variant THCA-SA 11 65365318 65365318 single base substitution T C 3_prime_UTR_variant THCA-SA 11 65365318 65365318 single base substitution T C downstream_gene_variant THCA-SA 11 65373458 65373458 single base substitution C A 3_prime_UTR_variant THCA-SA 11 65373458 65373458 single base substitution C A 5_prime_UTR_variant THCA-SA 11 65373458 65373458 single base substitution C A downstream_gene_variant THCA-SA 11 65373458 65373458 single base substitution C A exon_variant THCA-SA 11 65373458 65373458 single base substitution C A missense_variant W309C 927G>T THCA-SA 11 65373458 65373458 single base substitution C A missense_variant W566C 1698G>T THCA-SA 11 65386206 65386206 single base substitution C G upstream_gene_variant THCA-SA 11 65386261 65386261 single base substitution G A upstream_gene_variant UCEC-US 11 65361004 65361004 single base substitution C T downstream_gene_variant UCEC-US 11 65365772 65365772 single base substitution G A 3_prime_UTR_variant UCEC-US 11 65365772 65365772 single base substitution G A downstream_gene_variant UCEC-US 11 65365772 65365772 single base substitution G A missense_variant A261V 782C>T UCEC-US 11 65365772 65365772 single base substitution G A missense_variant A588V 1763C>T UCEC-US 11 65365772 65365772 single base substitution G A missense_variant A845V 2534C>T UCEC-US 11 65366882 65366882 single base substitution C T 3_prime_UTR_variant UCEC-US 11 65366882 65366882 single base substitution C T downstream_gene_variant UCEC-US 11 65366882 65366882 single base substitution C T missense_variant R146H 437G>A UCEC-US 11 65366882 65366882 single base substitution C T missense_variant R473H 1418G>A UCEC-US 11 65366882 65366882 single base substitution C T missense_variant R730H 2189G>A UCEC-US 11 65373232 65373232 single base substitution C A downstream_gene_variant UCEC-US 11 65373232 65373232 single base substitution C A exon_variant UCEC-US 11 65373232 65373232 single base substitution C A missense_variant G27C 79G>T UCEC-US 11 65373232 65373232 single base substitution C A missense_variant G354C 1060G>T UCEC-US 11 65373232 65373232 single base substitution C A missense_variant G611C 1831G>T UCEC-US 11 65373232 65373232 single base substitution C A splice_region_variant UCEC-US 11 65373292 65373292 single base substitution A G 3_prime_UTR_variant UCEC-US 11 65373292 65373292 single base substitution A G downstream_gene_variant UCEC-US 11 65373292 65373292 single base substitution A G exon_variant UCEC-US 11 65373292 65373292 single base substitution A G missense_variant Y334H 1000T>C UCEC-US 11 65373292 65373292 single base substitution A G missense_variant Y591H 1771T>C UCEC-US 11 65373292 65373292 single base substitution A G missense_variant Y7H 19T>C UCEC-US 11 65375136 65375136 single base substitution G A downstream_gene_variant UCEC-US 11 65375136 65375136 single base substitution G A exon_variant UCEC-US 11 65375136 65375136 single base substitution G A synonymous_variant F150F 450C>T UCEC-US 11 65375136 65375136 single base substitution G A synonymous_variant F407F 1221C>T UCEC-US 11 65375136 65375136 single base substitution G A upstream_gene_variant UCEC-US 11 65375752 65375752 single base substitution T C downstream_gene_variant UCEC-US 11 65375752 65375752 single base substitution T C exon_variant UCEC-US 11 65375752 65375752 single base substitution T C missense_variant S303G 907A>G UCEC-US 11 65375752 65375752 single base substitution T C missense_variant S46G 136A>G UCEC-US 11 65375752 65375752 single base substitution T C missense_variant S53G 157A>G UCEC-US 11 65375752 65375752 single base substitution T C upstream_gene_variant UCEC-US 11 65375814 65375814 single base substitution G A downstream_gene_variant UCEC-US 11 65375814 65375814 single base substitution G A exon_variant UCEC-US 11 65375814 65375814 single base substitution G A missense_variant A25V 74C>T UCEC-US 11 65375814 65375814 single base substitution G A missense_variant A282V 845C>T UCEC-US 11 65375814 65375814 single base substitution G A missense_variant A32V 95C>T UCEC-US 11 65375814 65375814 single base substitution G A upstream_gene_variant UCEC-US 11 65380717 65380717 single base substitution G A exon_variant UCEC-US 11 65380717 65380717 single base substitution G A intron_variant UCEC-US 11 65380717 65380717 single base substitution G A synonymous_variant L171L 511C>T UCEC-US 11 65380717 65380717 single base substitution G A upstream_gene_variant UCEC-US 11 65384320 65384320 single base substitution C T upstream_gene_variant UCEC-US 11 65385142 65385142 single base substitution G A upstream_gene_variant UCEC-US 11 65385983 65385983 single base substitution A G upstream_gene_variant UCEC-US 11 65387853 65387853 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 LIM2405 COSM4613271 c.1841delC p.P614fs*27 Deletion - Frameshift 11:65599759-65599759 - CHC892T COSM4793611 c.2401G>A p.A801T Substitution - Missense 11:65598434-65598434 - T3033 COSM4700284 c.56G>A p.S19N Substitution - Missense 11:65613701-65613701 - Au3 COSM5601775 c.432G>A p.K144K Substitution - coding silent 11:65613325-65613325 - PCSI_0090_Pa_P COSM3788025 c.128A>G p.N43S Substitution - Missense 11:65613629-65613629 - TCGA-22-4613-01 COSM689999 c.1115T>C p.I372T Substitution - Missense 11:65607771-65607771 - TCGA-BR-8361-01 COSM4035467 c.251G>T p.W84L Substitution - Missense 11:65613506-65613506 - TCGA-DA-A1I1-06 COSM3451843 c.1729C>T p.Q577* Substitution - Nonsense 11:65605956-65605956 - sysucc-1397T COSM5473200 c.1502G>A p.R501H Substitution - Missense 11:65606792-65606792 - HCC74T COSM1605024 c.2135T>A p.L712Q Substitution - Missense 11:65599465-65599465 - TCGA-76-6286-01 COSM3398047 c.1200G>A p.K400K Substitution - coding silent 11:65607686-65607686 - TCGA-B0-5712-01 COSM1239395 c.688C>T p.H230Y Substitution - Missense 11:65613069-65613069 - CSCC-38-T COSM4563080 c.957G>A p.E319E Substitution - coding silent 11:65608034-65608034 - TCGA-AC-A5XS-01 COSM4391075 c.358G>T p.E120* Substitution - Nonsense 11:65613399-65613399 - AOCS-078-1-9 COSM3980559 c.1931C>T p.A644V Substitution - Missense 11:65599669-65599669 - TCGA-AC-A5XS-01 COSM4391017 c.451G>A p.D151N Substitution - Missense 11:65613306-65613306 - TCGA-D1-A15X-01 COSM930455 c.907A>G p.S303G Substitution - Missense 11:65608281-65608281 - TCGA-EE-A2GR-06 COSM3451845 c.1150C>T p.L384L Substitution - coding silent 11:65607736-65607736 - T2417 COSM4700277 c.1948G>A p.A650T Substitution - Missense 11:65599652-65599652 - BN02 COSM1605026 c.543T>G p.A181A Substitution - coding silent 11:65613214-65613214 - 61 COSM5739318 c.1291C>T p.Q431* Substitution - Nonsense 11:65607468-65607468 - Pat_76_A COSM5839253 c.1246-1G>A p.? Unknown 11:65607514-65607514 - T2969 COSM4700282 c.674G>A p.G225E Substitution - Missense 11:65613083-65613083 - BN02T COSM1605026 c.543T>G p.A181A Substitution - coding silent 11:65613214-65613214 - 101047 COSM94664 c.628G>A p.V210M Substitution - Missense 11:65613129-65613129 - TCGA-BR-8382-01 COSM4035457 c.2427A>C p.S809S Substitution - coding silent 11:65598408-65598408 - 37M COSM5583741 c.1043C>T p.P348L Substitution - Missense 11:65607948-65607948 - 2492722 COSM5721729 c.592G>A p.G198S Substitution - Missense 11:65613165-65613165 - LUAD-F00162 COSM391661 c.308delG p.G103fs*20 Deletion - Frameshift 11:65613449-65613449 - 51T COSM110554 c.2047C>T p.P683S Substitution - Missense 11:65599553-65599553 - TCGA-B5-A11E-01 COSM930456 c.845C>T p.A282V Substitution - Missense 11:65608343-65608343 - ESO-859 COSM1239395 c.688C>T p.H230Y Substitution - Missense 11:65613069-65613069 - T2417 COSM4700275 c.2039C>T p.T680M Substitution - Missense 11:65599561-65599561 - T1764 COSM4700280 c.1225G>A p.E409K Substitution - Missense 11:65607661-65607661 - TCGA-HU-8245-01 COSM4035463 c.997G>A p.G333S Substitution - Missense 11:65607994-65607994 - AOCS-134-3-9 COSM1214389 c.2270G>A p.R757H Substitution - Missense 11:65598565-65598565 - RK047_C01 COSM1628168 c.694G>T p.E232* Substitution - Nonsense 11:65613063-65613063 - CSCC-62-T COSM4516514 c.1993_1994GG>AA p.G665K Substitution - Missense 11:65599606-65599607 - sysucc-774T COSM5461532 c.1069+10C>T p.? Unknown 11:65607912-65607912 - ESCC_55 COSM5631705 c.940G>A p.E314K Substitution - Missense 11:65608051-65608051 - T2269 COSM930454 c.1221C>T p.F407F Substitution - coding silent 11:65607665-65607665 - YUOMEGA COSM5373276 c.1049C>T p.P350L Substitution - Missense 11:65607942-65607942 - T2417 COSM3451842 c.2060C>T p.P687L Substitution - Missense 11:65599540-65599540 - AOCS-139-12-5 COSM3980561 c.324C>G p.P108P Substitution - coding silent 11:65613433-65613433 - GC_370T-GC_370N COSM4773147 c.1184T>A p.M395K Substitution - Missense 11:65607702-65607702 - HCC155 COSM3703610 c.1393G>A p.D465N Substitution - Missense 11:65607366-65607366 - 587338 COSM1214390 c.965A>G p.Y322C Substitution - Missense 11:65608026-65608026 - TCGA-A6-5661-01 COSM1355980 c.2240G>A p.R747H Substitution - Missense 11:65598595-65598595 - TCGA-G4-6586-01 COSM1355983 c.2118G>A p.P706P Substitution - coding silent 11:65599482-65599482 - T3080 COSM4700279 c.1341G>A p.Q447Q Substitution - coding silent 11:65607418-65607418 - CHC892T COSM4793687 c.1227G>A p.E409E Substitution - coding silent 11:65607659-65607659 - PTC_441 COSM5957363 c.1698G>T p.W566C Substitution - Missense 11:65605987-65605987 - 6115114 COSM5562910 c.2248C>T p.P750S Substitution - Missense 11:65598587-65598587 - YUMER COSM1704244 c.1204G>C p.E402Q Substitution - Missense 11:65607682-65607682 - HCC74 COSM1605024 c.2135T>A p.L712Q Substitution - Missense 11:65599465-65599465 - TCGA-BR-7851-01 COSM4035459 c.2050G>A p.A684T Substitution - Missense 11:65599550-65599550 - TCGA-EB-A41A-01 COSM3451843 c.1729C>T p.Q577* Substitution - Nonsense 11:65605956-65605956 - PCSI_0492_Pa_P_526 COSM4964818 c.1586G>C p.R529P Substitution - Missense 11:65606708-65606708 - TCGA-AA-3966-01 COSM272922 c.439C>T p.R147C Substitution - Missense 11:65613318-65613318 - TCGA-CM-5861-01 COSM1355984 c.2117C>T p.P706L Substitution - Missense 11:65599483-65599483 - 451 COSM1742462 c.377G>A p.G126E Substitution - Missense 11:65613380-65613380 - BN20T COSM1605025 c.735C>T p.N245N Substitution - coding silent 11:65613022-65613022 - 587256 COSM1214393 c.623G>A p.R208Q Substitution - Missense 11:65613134-65613134 - 587350 COSM1214391 c.2024C>T p.P675L Substitution - Missense 11:65599576-65599576 - BCB111T COSM4949834 c.2285G>T p.G762V Substitution - Missense 11:65598550-65598550 - TCGA-BR-8680-01 COSM4035466 c.440G>A p.R147H Substitution - Missense 11:65613317-65613317 - 2171660 COSM4422996 c.1750C>T p.R584C Substitution - Missense 11:65605842-65605842 - CSCC-29-T COSM4476053 c.2037C>T p.P679P Substitution - coding silent 11:65599563-65599563 - TCGA-BR-7707-01 COSM4035460 c.2006G>A p.R669H Substitution - Missense 11:65599594-65599594 - CHC892T COSM4793611 c.2401G>A p.A801T Substitution - Missense 11:65598434-65598434 - 1_PRE-TREATMENT COSM1719450 c.847G>A p.A283T Substitution - Missense 11:65608341-65608341 - AOCS-139-19-0 COSM3980561 c.324C>G p.P108P Substitution - coding silent 11:65613433-65613433 - HCC2998 COSM1676181 c.512T>G p.L171R Substitution - Missense 11:65613245-65613245 - 1_PRE-TREATMENT COSM1719449 c.2036C>T p.P679L Substitution - Missense 11:65599564-65599564 - PTC-28C COSM3998538 c.312C>T p.G104G Substitution - coding silent 11:65613445-65613445 - Br09P COSM39634 c.1976G>A p.R659H Substitution - Missense 11:65599624-65599624 - TCGA-AD-5900-01 COSM1355986 c.1080G>A p.A360A Substitution - coding silent 11:65607806-65607806 - S00836 COSM312730 c.2046G>A p.T682T Substitution - coding silent 11:65599554-65599554 - PT46 COSM5929297 c.322C>T p.P108S Substitution - Missense 11:65613435-65613435 - TCGA-JW-A5VK-01 COSM4855136 c.1125G>A p.Q375Q Substitution - coding silent 11:65607761-65607761 - T3152 COSM4700273 c.2476delC p.Q826fs*>22 Deletion - Frameshift 11:65598359-65598359 - T3080 COSM4700278 c.1585C>T p.R529W Substitution - Missense 11:65606709-65606709 - BD236T COSM5519058 c.1285C>T p.R429C Substitution - Missense 11:65607474-65607474 - TCGA-D7-6524-01 COSM4035461 c.1558G>A p.G520R Substitution - Missense 11:65606736-65606736 - BD115T COSM5500707 c.1304C>T p.A435V Substitution - Missense 11:65607455-65607455 - TCGA-DC-6682-01 COSM1561663 c.445G>A p.D149N Substitution - Missense 11:65613312-65613312 - Au10 COSM5598478 c.2454C>T p.A818A Substitution - coding silent 11:65598381-65598381 - sysucc-880T COSM5462069 c.1489+6G>T p.? Unknown 11:65607264-65607264 - TCGA-BP-5194-01 COSM467234 c.740-1G>T p.? Unknown 11:65608449-65608449 - 587278 COSM272922 c.439C>T p.R147C Substitution - Missense 11:65613318-65613318 - CSCC-27-T COSM4475088 c.1961C>T p.S654L Substitution - Missense 11:65599639-65599639 - TCGA-D5-6930-01 COSM3687526 c.2049C>T p.P683P Substitution - coding silent 11:65599551-65599551 - CSCC-5-T COSM2165950 c.2073C>T p.P691P Substitution - coding silent 11:65599527-65599527 - TCGA-BR-8363-01 COSM4035465 c.858C>T p.Y286Y Substitution - coding silent 11:65608330-65608330 - TCGA-DD-A3A9-01 COSM4920375 c.2410A>G p.T804A Substitution - Missense 11:65598425-65598425 - BD124T COSM5492825 c.882C>T p.I294I Substitution - coding silent 11:65608306-65608306 - TCGA-J9-A52C-01 COSM1355982 c.2205C>T p.R735R Substitution - coding silent 11:65599395-65599395 - 10-P1058 COSM4574667 c.2405C>T p.P802L Substitution - Missense 11:65598430-65598430 - TCGA-F5-6864-01 COSM194246 c.968G>A p.R323H Substitution - Missense 11:65608023-65608023 - TCGA-D3-A5GO-06 COSM3451840 c.2079C>T p.S693S Substitution - coding silent 11:65599521-65599521 - YULETA COSM3451843 c.1729C>T p.Q577* Substitution - Nonsense 11:65605956-65605956 - 2492723 COSM5721729 c.592G>A p.G198S Substitution - Missense 11:65613165-65613165 - AOCS-135-3-1 COSM3980560 c.1133C>T p.A378V Substitution - Missense 11:65607753-65607753 - HCC2998 COSM1676181 c.512T>G p.L171R Substitution - Missense 11:65613245-65613245 - T2932 COSM4700283 c.668C>T p.A223V Substitution - Missense 11:65613089-65613089 - PT23_1 COSM5902974 c.1245G>A p.K415K Substitution - coding silent 11:65607641-65607641 - T3724 COSM4700274 c.2106G>A p.T702T Substitution - coding silent 11:65599494-65599494 - TCGA-AP-A056-01 COSM930453 c.1771T>C p.Y591H Substitution - Missense 11:65605821-65605821 - TCGA-AA-3663-01 COSM1355987 c.656C>T p.A219V Substitution - Missense 11:65613101-65613101 - TCGA-B5-A11E-01 COSM930450 c.2534C>T p.A845V Substitution - Missense 11:65598301-65598301 - TCGA-D1-A16X-01 COSM930457 c.511C>T p.L171L Substitution - coding silent 11:65613246-65613246 - HRA19 COSM4637639 c.1044C>T p.P348P Substitution - coding silent 11:65607947-65607947 - AOCS-135-8-X COSM3980560 c.1133C>T p.A378V Substitution - Missense 11:65607753-65607753 - TCGA-A6-6653-01 COSM1355978 c.2471_2472insG p.Q826fs*>23 Insertion - Frameshift 11:65598363-65598364 - TCGA-D3-A2JH-06 COSM1704243 c.1709C>T p.S570F Substitution - Missense 11:65605976-65605976 - TCGA-A6-6781-01 COSM1355979 c.2351C>T p.A784V Substitution - Missense 11:65598484-65598484 - TCGA-FW-A3R5-06 COSM3869913 c.1647C>T p.P549P Substitution - coding silent 11:65606038-65606038 - TCGA-BH-A18G-01 COSM5218196 c.2471delG p.G824fs*>24 Deletion - Frameshift 11:65598364-65598364 - BCB111T COSM4949834 c.2285G>T p.G762V Substitution - Missense 11:65598550-65598550 - MOLT-4 COSM1676182 c.364G>A p.V122M Substitution - Missense 11:65613393-65613393 - TCGA-D5-6920-01 COSM1355981 c.2228C>T p.P743L Substitution - Missense 11:65598607-65598607 - T368 COSM4700281 c.930G>A p.V310V Substitution - coding silent 11:65608061-65608061 - STC297 COSM5051025 c.1501C>T p.R501C Substitution - Missense 11:65606793-65606793 - SC_9008 COSM4613271 c.1841delC p.P614fs*27 Deletion - Frameshift 11:65599759-65599759 - C086 COSM2165993 c.287C>T p.P96L Substitution - Missense 11:65613470-65613470 - TCGA-12-0688-01 COSM3747895 c.69T>G p.G23G Substitution - coding silent 11:65613688-65613688 - 100879 COSM94663 c.1731G>C p.Q577H Substitution - Missense 11:65605954-65605954 - 7b COSM4657704 c.1102G>C p.D368H Substitution - Missense 11:65607784-65607784 - BD124T COSM5492824 c.2070G>A p.P690P Substitution - coding silent 11:65599530-65599530 - 1_RESISTANT COSM1719449 c.2036C>T p.P679L Substitution - Missense 11:65599564-65599564 - TCGA-E7-A3Y1-01 COSM3791804 c.885G>A p.K295K Substitution - coding silent 11:65608303-65608303 - 64 COSM2165981 c.670C>T p.R224C Substitution - Missense 11:65613087-65613087 - LIM1215 COSM4639346 c.2513A>G p.Q838R Substitution - Missense 11:65598322-65598322 - CSCC-31-T COSM4476158 c.2048C>T p.P683L Substitution - Missense 11:65599552-65599552 - TCGA-G3-A5SL-01 COSM4929562 c.512T>A p.L171Q Substitution - Missense 11:65613245-65613245 - BD221T COSM5496393 c.600C>T p.P200P Substitution - coding silent 11:65613157-65613157 - 2492720 COSM5721729 c.592G>A p.G198S Substitution - Missense 11:65613165-65613165 - 107529 COSM96007 c.12G>A p.L4L Substitution - coding silent 11:65613745-65613745 - SC_9018 COSM96007 c.12G>A p.L4L Substitution - coding silent 11:65613745-65613745 - 587316 COSM1214389 c.2270G>A p.R757H Substitution - Missense 11:65598565-65598565 - TCGA-D3-A1Q6-06 COSM3451846 c.915C>T p.V305V Substitution - coding silent 11:65608273-65608273 - TCGA-EE-A3AE-06 COSM3451844 c.1263G>A p.E421E Substitution - coding silent 11:65607496-65607496 - TCGA-EE-A3JI-06 COSM3451839 c.2301T>A p.P767P Substitution - coding silent 11:65598534-65598534 - CSCC-31-T COSM4471312 c.1710C>T p.S570S Substitution - coding silent 11:65605975-65605975 - TCGA-18-3409-01 COSM690000 c.1807C>T p.P603S Substitution - Missense 11:65605785-65605785 - CSCC-47-T COSM4460374 c.1163C>T p.P388L Substitution - Missense 11:65607723-65607723 - 12924 COSM5613440 c.2203C>A p.R735S Substitution - Missense 11:65599397-65599397 - PT14_1 COSM2165957 c.1811C>T p.S604F Substitution - Missense 11:65605781-65605781 - ESO-752 COSM1257262 c.484C>T p.R162C Substitution - Missense 11:65613273-65613273 - T3446 COSM4700276 c.1988C>T p.P663L Substitution - Missense 11:65599612-65599612 - TCGA-D8-A13Y-01 COSM429611 c.1269G>A p.E423E Substitution - coding silent 11:65607490-65607490 - TCGA-HC-8266-01 COSM4392824 c.1092C>T p.H364H Substitution - coding silent 11:65607794-65607794 - TCGA-EE-A2MI-06 COSM3451841 c.2063C>T p.T688I Substitution - Missense 11:65599537-65599537 - TCGA-EE-A3JB-06 COSM4898811 c.2203C>T p.R735C Substitution - Missense 11:65599397-65599397 - 2492721 COSM5721729 c.592G>A p.G198S Substitution - Missense 11:65613165-65613165 - TCGA-BG-A0W2-01 COSM930451 c.2189G>A p.R730H Substitution - Missense 11:65599411-65599411 - S00472 COSM5657655 c.1251A>G p.L417L Substitution - coding silent 11:65607508-65607508 - C086 COSM5534247 c.2314C>T p.L772F Substitution - Missense 11:65598521-65598521 - AOCS-139-1-5 COSM3980561 c.324C>G p.P108P Substitution - coding silent 11:65613433-65613433 - HCC155T COSM3703610 c.1393G>A p.D465N Substitution - Missense 11:65607366-65607366 - TCGA-B5-A11Y-01 COSM930452 c.1831G>T p.G611C Substitution - Missense 11:65605761-65605761 - BN20 COSM1605025 c.735C>T p.N245N Substitution - coding silent 11:65613022-65613022 - TCGA-CG-4306-01 COSM4035458 c.2421G>A p.P807P Substitution - coding silent 11:65598414-65598414 - 587342 COSM1214392 c.608G>A p.R203Q Substitution - Missense 11:65613149-65613149 - TCGA-EE-A29L-06 COSM3451842 c.2060C>T p.P687L Substitution - Missense 11:65599540-65599540 - AOCS-139-6-3 COSM3980561 c.324C>G p.P108P Substitution - coding silent 11:65613433-65613433 - LUAD-D02185 COSM338452 c.1123C>G p.Q375E Substitution - Missense 11:65607763-65607763 - NCI-H322M COSM1194885 c.526A>G p.I176V Substitution - Missense 11:65613231-65613231 - TCGA-G4-6588-01 COSM1355982 c.2205C>T p.R735R Substitution - coding silent 11:65599395-65599395 - YUKLAB COSM1704243 c.1709C>T p.S570F Substitution - Missense 11:65605976-65605976 - CHC892T COSM4793687 c.1227G>A p.E409E Substitution - coding silent 11:65607659-65607659 - T36 COSM4613271 c.1841delC p.P614fs*27 Deletion - Frameshift 11:65599759-65599759 - 2492729 COSM5729779 c.1401G>A p.E467E Substitution - coding silent 11:65607358-65607358 - H358 COSM1193965 c.530T>C p.I177T Substitution - Missense 11:65613227-65613227 - PD7321a COSM5769185 c.1860C>T p.P620P Substitution - coding silent 11:65599740-65599740 - H322T COSM1194885 c.526A>G p.I176V Substitution - Missense 11:65613231-65613231 - 107529 COSM96006 c.789G>A p.L263L Substitution - coding silent 11:65608399-65608399 - CSCC-56-T COSM4485324 c.291C>T p.S97S Substitution - coding silent 11:65613466-65613466 - TCGA-CM-4743-01 COSM1355985 c.1648delC p.R550fs*51 Deletion - Frameshift 11:65606037-65606037 - TCGA-39-5031-01 COSM96006 c.789G>A p.L263L Substitution - coding silent 11:65608399-65608399 - 2173 COSM5015025 c.2165A>T p.Q722L Substitution - Missense 11:65599435-65599435 - SNUH_G16_S1 COSM3998538 c.312C>T p.G104G Substitution - coding silent 11:65613445-65613445 - TCGA-CD-A4MG-01 COSM4035462 c.1364G>A p.R455H Substitution - Missense 11:65607395-65607395 - 3N48-VS-3T48 COSM4982678 c.1090C>T p.H364Y Substitution - Missense 11:65607796-65607796 - TCGA-AO-A03V-01 COSM429610 c.2543G>C p.*848S Nonstop extension 11:65598292-65598292 - TCGA-B7-5816-01 COSM4035464 c.960G>A p.V320V Substitution - coding silent 11:65608031-65608031 - TCGA-D1-A16X-01 COSM930454 c.1221C>T p.F407F Substitution - coding silent 11:65607665-65607665 - TCGA-EE-A2GI-06 COSM3451847 c.360G>A p.E120E Substitution - coding silent 11:65613397-65613397 - BZ04 COSM5757796 c.2467G>T p.G823W Substitution - Missense 11:65598368-65598368 - RK219_C01 COSM3739230 c.2156C>G p.P719R Substitution - Missense 11:65599444-65599444 - HCC054T COSM5809576 c.2408G>T p.W803L Substitution - Missense 11:65598427-65598427 - STC291 COSM5051026 c.1057C>T p.Q353* Substitution - Nonsense 11:65607934-65607934 - TCGA-28-5214-01 COSM3398046 c.2070G>T p.P690P Substitution - coding silent 11:65599530-65599530 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.502872 11q13.1-q13.3 600050 2406298|CGAP|BC011263|A/G|non-coding||3468|Validated; 2406298|CGAP|BC064543|A/G|non-coding||3439|Validated; 2406299|CGAP|BC011263|C/T|non-coding||3501|Candidate; 2406299|CGAP|BC064543|C/T|non-coding||3472|Candidate; 2406300|CGAP|BC011263|C/T|non-coding||3212|Candidate; 2406300|CGAP|BC064543|C/T|non-coding||3183|Candidate; 1527382|dbSNP|BC011263|A/G|non-coding||3468|Candidate; 1527382|dbSNP|BC064543|A/G|non-coding||3439|Candidate; 1527384|dbSNP|BC011263|C/T|non-coding||3501|Candidate; 1527384|dbSNP|BC064543|C/T|non-coding||3472|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I372T c.1115T>C 11 65375242 LUSC A T Synonymous p.P767P c.2301T>A 11 65366005 CM C A IntronicSNV . c.740-108G>T 11 65376027 HC C A Missense p.A352S c.1054G>T 11 65375408 LUAD C A Missense p.G520W c.1558G>T 11 65374207 LUAD C A Missense p.G611C c.1831G>T 11 65373232 UCEC C A Nonsense p.E232* c.694G>T 11 65380534 HC C A SpliceAcceptorSNV . c.740-1G>T 11 65375920 RCCC C A Synonymous p.P690P c.2070G>T 11 65367001 GBM C - Frameshift p.G824Afs*111 c.2471delG 11 65365835 STAD C G 3-UTRSNV . c.2541+2G>C 11 65365763 BRCA C G Missense p.K413N c.1239G>C 11 65375118 LUAD C G Missense p.R529P c.1586G>C 11 65374179 CM C T Missense p.A335T c.1003G>A 11 65375459 LUAD C T Missense p.D304N c.910G>A 11 65375749 LUAD C T Missense p.G520R c.1558G>A 11 65374207 STAD C T Missense p.R581K c.1742G>A 11 65373321 LUAD C T Missense p.V210M c.628G>A 11 65380600 HNSC C T Synonymous p.E120E c.360G>A 11 65380868 CM C T Synonymous p.L263L c.789G>A 11 65375870 LUSC C T Synonymous p.P807P c.2421G>A 11 65365885 STAD C T Synonymous p.T682T c.2046G>A 11 65367025 SCLC C T Synonymous p.V320V c.960G>A 11 65375502 STAD G A Missense p.H230Y c.688C>T 11 65380540 ESCA G A Missense p.P599S c.1795C>T 11 65373268 CM G A Missense p.P687L c.2060C>T 11 65367011 CM G A Missense p.P778L c.2333C>T 11 65365973 CM G A Missense p.P778S c.2332C>T 11 65365974 CM G A Missense p.R659H c.1976G>A 11 65367095 GBM G A Missense p.R775C c.2323C>T 11 65365983 CM G A Missense p.S570F c.1709C>T 11 65373447 CM G A Missense p.T688I c.2063C>T 11 65367008 CM G A Nonsense p.Q577* c.1729C>T 11 65373427 CM G A Synonymous p.H364H c.1092C>T 11 65375265 PRAD G A Synonymous p.I718I c.2154C>T 11 65366917 CM G A Synonymous p.L242L c.726C>T 11 65380502 CM G A Synonymous p.L384L c.1150C>T 11 65375207 CM G A Synonymous p.V305V c.915C>T 11 65375744 CM GG AA Missense p.P628L c.1883_1884delinsTT 11 65367187 CM G T Missense p.R735S c.2203C>A 11 65366868 NSCLC G T Synonymous p.I176I c.528C>A 11 65380700 HNSC