Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 5530029 5530029 + Missense_Mutation SNP G G T TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr11:5530029G>T c.760C>A c.(760-762)Ctt>Att p.L254I BLCA 11 5528897 5528897 + Missense_Mutation SNP C C G TCGA-E7-A6ME-01A-22D-A32B-08 TCGA-E7-A6ME-10B-01D-A329-08 g.chr11:5528897C>G c.1892G>C c.(1891-1893)cGt>cCt p.R631P BLCA 11 5529035 5529035 + Missense_Mutation SNP G G A TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr11:5529035G>A c.1754C>T c.(1753-1755)tCt>tTt p.S585F BLCA 11 5529441 5529441 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:5529441C>A c.1348G>T c.(1348-1350)Gat>Tat p.D450Y BLCA 11 5530371 5530371 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:5530371G>A c.418C>T c.(418-420)Ctc>Ttc p.L140F BLCA 11 5530516 5530516 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr11:5530516G>A c.273C>T c.(271-273)atC>atT p.I91I BRCA 11 5529582 5529582 + Missense_Mutation SNP T T G TCGA-AQ-A0Y5-01A-11D-A14K-09 TCGA-AQ-A0Y5-10A-01D-A17G-09 g.chr11:5529582T>G c.1207A>C c.(1207-1209)Atc>Ctc p.I403L BRCA 11 5529922 5529922 + Silent SNP G G A TCGA-EW-A1IW-01A-11D-A13L-09 TCGA-EW-A1IW-10A-01D-A13O-09 g.chr11:5529922G>A c.867C>T c.(865-867)acC>acT p.T289T BRCA 11 5530467 5530467 + Missense_Mutation SNP G G A TCGA-AR-A24N-01A-11D-A167-09 TCGA-AR-A24N-10A-01D-A167-09 g.chr11:5530467G>A c.322C>T c.(322-324)Cct>Tct p.P108S CESC 11 5529679 5529679 + Silent SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr11:5529679G>A c.1110C>T c.(1108-1110)agC>agT p.S370S CESC 11 5529891 5529891 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:5529891C>G c.898G>C c.(898-900)Gac>Cac p.D300H COAD 11 5528825 5528825 + Missense_Mutation SNP G G A TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr11:5528825G>A c.1964C>T c.(1963-1965)tCg>tTg p.S655L COAD 11 5528925 5528925 + Missense_Mutation SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:5528925G>T c.1864C>A c.(1864-1866)Caa>Aaa p.Q622K COAD 11 5528951 5528951 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:5528951T>C c.1838A>G c.(1837-1839)gAg>gGg p.E613G COAD 11 5529111 5529111 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:5529111C>T c.1678G>A c.(1678-1680)Gag>Aag p.E560K COAD 11 5529314 5529314 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:5529314T>C c.1475A>G c.(1474-1476)aAt>aGt p.N492S COAD 11 5529332 5529332 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:5529332A>G c.1457T>C c.(1456-1458)cTg>cCg p.L486P COAD 11 5529384 5529384 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:5529384G>A c.1405C>T c.(1405-1407)Cct>Tct p.P469S COAD 11 5529441 5529441 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:5529441C>A c.1348G>T c.(1348-1350)Gat>Tat p.D450Y COAD 11 5529472 5529472 + Silent SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr11:5529472T>C c.1317A>G c.(1315-1317)acA>acG p.T439T COAD 11 5529474 5529474 + Missense_Mutation SNP T T C TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:5529474T>C c.1315A>G c.(1315-1317)Aca>Gca p.T439A COAD 11 5529594 5529594 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:5529594C>T c.1195G>A c.(1195-1197)Gag>Aag p.E399K COAD 11 5529665 5529665 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr11:5529665G>T c.1124C>A c.(1123-1125)cCa>cAa p.P375Q COAD 11 5529961 5529961 + Silent SNP A A G TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:5529961A>G c.828T>C c.(826-828)aaT>aaC p.N276N COAD 11 5530400 5530400 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:5530400delG c.389delC c.(388-390)cctfs p.P130fs COAD 11 5530614 5530614 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:5530614C>T c.175G>A c.(175-177)Gat>Aat p.D59N COAD 11 5530615 5530615 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:5530615G>A c.174C>T c.(172-174)ccC>ccT p.P58P COAD 11 5530754 5530754 + Missense_Mutation SNP C C G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr11:5530754C>G c.35G>C c.(34-36)aGc>aCc p.S12T COADREAD 11 5528825 5528825 + Missense_Mutation SNP G G A TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr11:5528825G>A c.1964C>T c.(1963-1965)tCg>tTg p.S655L COADREAD 11 5528925 5528925 + Missense_Mutation SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:5528925G>T c.1864C>A c.(1864-1866)Caa>Aaa p.Q622K COADREAD 11 5528951 5528951 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:5528951T>C c.1838A>G c.(1837-1839)gAg>gGg p.E613G COADREAD 11 5528988 5528988 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:5528988C>A c.1801G>T c.(1801-1803)Gat>Tat p.D601Y COADREAD 11 5529111 5529111 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:5529111C>T c.1678G>A c.(1678-1680)Gag>Aag p.E560K COADREAD 11 5529314 5529314 + Missense_Mutation SNP T T C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:5529314T>C c.1475A>G c.(1474-1476)aAt>aGt p.N492S COADREAD 11 5529332 5529332 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:5529332A>G c.1457T>C c.(1456-1458)cTg>cCg p.L486P COADREAD 11 5529384 5529384 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:5529384G>A c.1405C>T c.(1405-1407)Cct>Tct p.P469S COADREAD 11 5529441 5529441 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:5529441C>A c.1348G>T c.(1348-1350)Gat>Tat p.D450Y COADREAD 11 5529472 5529472 + Silent SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr11:5529472T>C c.1317A>G c.(1315-1317)acA>acG p.T439T COADREAD 11 5529474 5529474 + Missense_Mutation SNP T T C TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:5529474T>C c.1315A>G c.(1315-1317)Aca>Gca p.T439A COADREAD 11 5529594 5529594 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:5529594C>T c.1195G>A c.(1195-1197)Gag>Aag p.E399K COADREAD 11 5529665 5529665 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr11:5529665G>T c.1124C>A c.(1123-1125)cCa>cAa p.P375Q COADREAD 11 5529738 5529738 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:5529738C>T c.1051G>A c.(1051-1053)Gag>Aag p.E351K COADREAD 11 5529961 5529961 + Silent SNP A A G TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:5529961A>G c.828T>C c.(826-828)aaT>aaC p.N276N COADREAD 11 5530318 5530318 + Silent SNP C C A TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chr11:5530318C>A c.471G>T c.(469-471)ctG>ctT p.L157L COADREAD 11 5530400 5530400 + Frame_Shift_Del DEL G G - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:5530400delG c.389delC c.(388-390)cctfs p.P130fs COADREAD 11 5530440 5530440 + Missense_Mutation SNP G G C TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr11:5530440G>C c.349C>G c.(349-351)Ctc>Gtc p.L117V COADREAD 11 5530484 5530484 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:5530484C>T c.305G>A c.(304-306)tGc>tAc p.C102Y COADREAD 11 5530614 5530614 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:5530614C>T c.175G>A c.(175-177)Gat>Aat p.D59N COADREAD 11 5530615 5530615 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:5530615G>A c.174C>T c.(172-174)ccC>ccT p.P58P COADREAD 11 5530754 5530754 + Missense_Mutation SNP C C G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr11:5530754C>G c.35G>C c.(34-36)aGc>aCc p.S12T ESCA 11 5529456 5529456 + Missense_Mutation SNP C C G TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr11:5529456C>G c.1333G>C c.(1333-1335)Gtc>Ctc p.V445L ESCA 11 5529807 5529807 + Missense_Mutation SNP C C A TCGA-IG-A5S3-01A-11D-A28B-09 TCGA-IG-A5S3-10A-01D-A28E-09 g.chr11:5529807C>A c.982G>T c.(982-984)Gac>Tac p.D328Y ESCA 11 5530157 5530157 + Missense_Mutation SNP A A C TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr11:5530157A>C c.632T>G c.(631-633)cTt>cGt p.L211R ESCA 11 5530201 5530201 + Missense_Mutation SNP A A T TCGA-L5-A8NN-01A-11D-A37C-09 TCGA-L5-A8NN-11A-11D-A37F-09 g.chr11:5530201A>T c.588T>A c.(586-588)caT>caA p.H196Q ESCA 11 5530262 5530262 + Missense_Mutation SNP A A G TCGA-L5-A8NF-01A-11D-A37C-09 TCGA-L5-A8NF-11A-11D-A37F-09 g.chr11:5530262A>G c.527T>C c.(526-528)tTc>tCc p.F176S GBM 11 5529018 5529018 + Missense_Mutation SNP G G A TCGA-32-5222-01A-01D-1486-08 TCGA-32-5222-10A-01D-1486-08 g.chr11:5529018G>A c.1771C>T c.(1771-1773)Ctt>Ttt p.L591F GBM 11 5529360 5529360 + Silent SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr11:5529360G>A c.1429C>T c.(1429-1431)Ctg>Ttg p.L477L GBM 11 5529867 5529867 + Missense_Mutation SNP A A T TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr11:5529867A>T c.922T>A c.(922-924)Tcc>Acc p.S308T GBMLGG 11 5529018 5529018 + Missense_Mutation SNP G G A TCGA-32-5222-01A-01D-1486-08 TCGA-32-5222-10A-01D-1486-08 g.chr11:5529018G>A c.1771C>T c.(1771-1773)Ctt>Ttt p.L591F GBMLGG 11 5529360 5529360 + Silent SNP G G A TCGA-19-4068-01A-01D-1353-08 TCGA-19-4068-10A-01D-1353-08 g.chr11:5529360G>A c.1429C>T c.(1429-1431)Ctg>Ttg p.L477L GBMLGG 11 5529867 5529867 + Missense_Mutation SNP A A T TCGA-06-0686-01A-01W-0348-08 TCGA-06-0686-10A-01W-0348-08 g.chr11:5529867A>T c.922T>A c.(922-924)Tcc>Acc p.S308T GBMLGG 11 5529965 5529965 + Missense_Mutation SNP C C T TCGA-FG-A4MU-01B-11D-A289-08 TCGA-FG-A4MU-10A-01D-A289-08 g.chr11:5529965C>T c.824G>A c.(823-825)gGc>gAc p.G275D GBMLGG 11 5530632 5530632 + Missense_Mutation SNP G G A TCGA-DU-8161-01A-11D-2253-08 TCGA-DU-8161-10A-01D-2253-08 g.chr11:5530632G>A c.157C>T c.(157-159)Cgc>Tgc p.R53C HNSC 11 5529368 5529368 + Missense_Mutation SNP G G T TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr11:5529368G>T c.1421C>A c.(1420-1422)cCt>cAt p.P474H HNSC 11 5529406 5529406 + Silent SNP A A G TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chr11:5529406A>G c.1383T>C c.(1381-1383)tcT>tcC p.S461S HNSC 11 5529680 5529680 + Missense_Mutation SNP C C T TCGA-IQ-A61O-01A-11D-A30E-08 TCGA-IQ-A61O-10A-01D-A30H-08 g.chr11:5529680C>T c.1109G>A c.(1108-1110)aGc>aAc p.S370N HNSC 11 5529987 5529987 + Missense_Mutation SNP C C T TCGA-CV-5436-01A-01D-1512-08 TCGA-CV-5436-10A-01D-1870-08 g.chr11:5529987C>T c.802G>A c.(802-804)Gca>Aca p.A268T HNSC 11 5530115 5530115 + Missense_Mutation SNP C C T TCGA-MT-A67A-01A-11D-A30E-08 TCGA-MT-A67A-10A-01D-A30H-08 g.chr11:5530115C>T c.674G>A c.(673-675)cGt>cAt p.R225H HNSC 11 5530434 5530434 + Missense_Mutation SNP G G C TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr11:5530434G>C c.355C>G c.(355-357)Cag>Gag p.Q119E HNSC 11 5530436 5530436 + Missense_Mutation SNP G G T TCGA-CV-7242-01A-11D-2012-08 TCGA-CV-7242-10A-01D-2013-08 g.chr11:5530436G>T c.353C>A c.(352-354)cCt>cAt p.P118H HNSC 11 5530480 5530480 + Silent SNP T T G TCGA-CN-6024-01A-11D-1683-08 TCGA-CN-6024-10A-01D-1683-08 g.chr11:5530480T>G c.309A>C c.(307-309)ccA>ccC p.P103P KICH 11 5530008 5530008 + Missense_Mutation SNP T T C TCGA-KN-8432-01A-11D-2310-10 TCGA-KN-8432-11A-01D-2311-10 g.chr11:5530008T>C c.781A>G c.(781-783)Att>Gtt p.I261V KIPAN 11 5528857 5528857 + Silent SNP G G A TCGA-B0-5710-01A-11D-1669-08 TCGA-B0-5710-11A-01D-1669-08 g.chr11:5528857G>A c.1932C>T c.(1930-1932)gaC>gaT p.D644D KIPAN 11 5529517 5529517 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:5529517A>G c.1272T>C c.(1270-1272)ggT>ggC p.G424G KIPAN 11 5530008 5530008 + Missense_Mutation SNP T T C TCGA-KN-8432-01A-11D-2310-10 TCGA-KN-8432-11A-01D-2311-10 g.chr11:5530008T>C c.781A>G c.(781-783)Att>Gtt p.I261V KIPAN 11 5530266 5530266 + Missense_Mutation SNP G G T TCGA-Y8-A8S1-01A-11D-A36X-10 TCGA-Y8-A8S1-10A-01D-A370-10 g.chr11:5530266G>T c.523C>A c.(523-525)Ccc>Acc p.P175T KIRC 11 5528857 5528857 + Silent SNP G G A TCGA-B0-5710-01A-11D-1669-08 TCGA-B0-5710-11A-01D-1669-08 g.chr11:5528857G>A c.1932C>T c.(1930-1932)gaC>gaT p.D644D KIRC 11 5529517 5529517 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:5529517A>G c.1272T>C c.(1270-1272)ggT>ggC p.G424G KIRP 11 5530266 5530266 + Missense_Mutation SNP G G T TCGA-Y8-A8S1-01A-11D-A36X-10 TCGA-Y8-A8S1-10A-01D-A370-10 g.chr11:5530266G>T c.523C>A c.(523-525)Ccc>Acc p.P175T LGG 11 5529965 5529965 + Missense_Mutation SNP C C T TCGA-FG-A4MU-01B-11D-A289-08 TCGA-FG-A4MU-10A-01D-A289-08 g.chr11:5529965C>T c.824G>A c.(823-825)gGc>gAc p.G275D LGG 11 5530632 5530632 + Missense_Mutation SNP G G A TCGA-DU-8161-01A-11D-2253-08 TCGA-DU-8161-10A-01D-2253-08 g.chr11:5530632G>A c.157C>T c.(157-159)Cgc>Tgc p.R53C LIHC 11 5528949 5528949 + Missense_Mutation SNP C C G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr11:5528949C>G c.1840G>C c.(1840-1842)Gct>Cct p.A614P LIHC 11 5529136 5529136 + Silent SNP C C A TCGA-DD-A4NG-01A-11D-A27I-10 TCGA-DD-A4NG-10A-01D-A27I-10 g.chr11:5529136C>A c.1653G>T c.(1651-1653)ggG>ggT p.G551G LIHC 11 5529234 5529234 + Frame_Shift_Del DEL G G - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr11:5529234delG c.1555delC c.(1555-1557)cgtfs p.R519fs LIHC 11 5530073 5530073 + Missense_Mutation SNP C C G TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr11:5530073C>G c.716G>C c.(715-717)cGg>cCg p.R239P LUAD 11 5528910 5528910 + Missense_Mutation SNP C C G TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr11:5528910C>G c.1879G>C c.(1879-1881)Ggc>Cgc p.G627R LUAD 11 5528911 5528911 + Missense_Mutation SNP C C A TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr11:5528911C>A c.1878G>T c.(1876-1878)atG>atT p.M626I LUAD 11 5529023 5529023 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:5529023C>A c.1766G>T c.(1765-1767)gGc>gTc p.G589V LUAD 11 5529338 5529338 + Missense_Mutation SNP C C T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr11:5529338C>T c.1451G>A c.(1450-1452)aGa>aAa p.R484K LUAD 11 5529464 5529464 + Missense_Mutation SNP G G C TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr11:5529464G>C c.1325C>G c.(1324-1326)cCt>cGt p.P442R LUAD 11 5529501 5529501 + Missense_Mutation SNP C C A TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chr11:5529501C>A c.1288G>T c.(1288-1290)Gca>Tca p.A430S LUAD 11 5529609 5529609 + Missense_Mutation SNP G G T TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr11:5529609G>T c.1180C>A c.(1180-1182)Cag>Aag p.Q394K LUAD 11 5529627 5529627 + Nonsense_Mutation SNP G G A TCGA-97-7547-01A-11D-2036-08 TCGA-97-7547-10A-01D-2036-08 g.chr11:5529627G>A c.1162C>T c.(1162-1164)Cag>Tag p.Q388* LUAD 11 5529784 5529784 + Missense_Mutation SNP G G C TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:5529784G>C c.1005C>G c.(1003-1005)aaC>aaG p.N335K LUAD 11 5529825 5529825 + Missense_Mutation SNP C C A TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr11:5529825C>A c.964G>T c.(964-966)Ggg>Tgg p.G322W LUAD 11 5529959 5529959 + Missense_Mutation SNP G G A TCGA-MP-A4T7-01A-11D-A24P-08 TCGA-MP-A4T7-10A-01D-A24P-08 g.chr11:5529959G>A c.830C>T c.(829-831)cCc>cTc p.P277L LUAD 11 5530050 5530050 + Missense_Mutation SNP T T G TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr11:5530050T>G c.739A>C c.(739-741)Att>Ctt p.I247L LUAD 11 5530072 5530072 + Silent SNP C C A TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr11:5530072C>A c.717G>T c.(715-717)cgG>cgT p.R239R LUAD 11 5530285 5530285 + Silent SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr11:5530285C>A c.504G>T c.(502-504)gtG>gtT p.V168V LUAD 11 5530472 5530472 + Missense_Mutation SNP G G C TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr11:5530472G>C c.317C>G c.(316-318)tCt>tGt p.S106C LUAD 11 5530488 5530488 + Missense_Mutation SNP C C T TCGA-97-8176-01A-11D-2393-08 TCGA-97-8176-10B-01D-2393-08 g.chr11:5530488C>T c.301G>A c.(301-303)Gag>Aag p.E101K LUAD 11 5530523 5530523 + Missense_Mutation SNP A A T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr11:5530523A>T c.266T>A c.(265-267)cTg>cAg p.L89Q LUAD 11 5530631 5530631 + Missense_Mutation SNP C C T TCGA-38-4629-01A-02D-1265-08 TCGA-38-4629-11A-01D-1265-08 g.chr11:5530631C>T c.158G>A c.(157-159)cGc>cAc p.R53H LUAD 11 5530649 5530649 + Missense_Mutation SNP T T A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr11:5530649T>A c.140A>T c.(139-141)aAg>aTg p.K47M LUAD 11 5530683 5530683 + Missense_Mutation SNP A A T TCGA-44-6145-01A-11D-1753-08 TCGA-44-6145-10A-01D-1753-08 g.chr11:5530683A>T c.106T>A c.(106-108)Tca>Aca p.S36T LUAD 11 5530706 5530706 + Missense_Mutation SNP G G T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:5530706G>T c.83C>A c.(82-84)aCg>aAg p.T28K LUSC 11 5529151 5529151 + Missense_Mutation SNP C C T TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr11:5529151C>T c.1638G>A c.(1636-1638)atG>atA p.M546I LUSC 11 5529258 5529258 + Missense_Mutation SNP G G A TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr11:5529258G>A c.1531C>T c.(1531-1533)Ctt>Ttt p.L511F LUSC 11 5529375 5529375 + Missense_Mutation SNP G G T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr11:5529375G>T c.1414C>A c.(1414-1416)Cct>Act p.P472T LUSC 11 5529644 5529644 + Frame_Shift_Del DEL G G - TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr11:5529644delG c.1145delC c.(1144-1146)ccafs p.P382fs LUSC 11 5530016 5530016 + Missense_Mutation SNP T T C TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr11:5530016T>C c.773A>G c.(772-774)tAc>tGc p.Y258C LUSC 11 5530073 5530073 + Missense_Mutation SNP C C A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:5530073C>A c.716G>T c.(715-717)cGg>cTg p.R239L LUSC 11 5530093 5530093 + Missense_Mutation SNP C C A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr11:5530093C>A c.696G>T c.(694-696)gaG>gaT p.E232D LUSC 11 5530345 5530345 + Silent SNP A A G TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr11:5530345A>G c.444T>C c.(442-444)cgT>cgC p.R148R OV 11 5528898 5528898 + Missense_Mutation SNP G G C TCGA-36-1571-01A-01W-0615-10 TCGA-36-1571-10A-01W-0615-10 g.chr11:5528898G>C c.1891C>G c.(1891-1893)Cgt>Ggt p.R631G OV 11 5529473 5529473 + Missense_Mutation SNP G G A TCGA-24-2267-01A-01W-0799-08 TCGA-24-2267-11A-01W-0799-08 g.chr11:5529473G>A c.1316C>T c.(1315-1317)aCa>aTa p.T439I OV 11 5530137 5530137 + Missense_Mutation SNP G G A TCGA-13-0893-01B-01W-0494-09 TCGA-13-0893-10A-01W-0494-09 g.chr11:5530137G>A c.652C>T c.(652-654)Cgg>Tgg p.R218W PAAD 11 5529987 5529987 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:5529987C>T c.802G>A c.(802-804)Gca>Aca p.A268T PAAD 11 5530082 5530082 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:5530082C>T c.707G>A c.(706-708)aGc>aAc p.S236N PAAD 11 5530259 5530259 + Missense_Mutation SNP A A T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:5530259A>T c.530T>A c.(529-531)aTc>aAc p.I177N PAAD 11 5530451 5530451 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:5530451C>A c.338G>T c.(337-339)aGt>aTt p.S113I PRAD 11 5529067 5529067 + Missense_Mutation SNP A A C TCGA-VN-A88K-01A-11D-A34U-08 TCGA-VN-A88K-10A-01D-A34X-08 g.chr11:5529067A>C c.1722T>G c.(1720-1722)aaT>aaG p.N574K PRAD 11 5529391 5529391 + Silent SNP T T C TCGA-CH-5763-01A-11D-1576-08 TCGA-CH-5763-11A-01D-1576-08 g.chr11:5529391T>C c.1398A>G c.(1396-1398)gcA>gcG p.A466A PRAD 11 5530165 5530165 + Silent SNP C C T TCGA-XJ-A9DX-01A-11D-A377-08 TCGA-XJ-A9DX-10A-01D-A37A-08 g.chr11:5530165C>T c.624G>A c.(622-624)ggG>ggA p.G208G READ 11 5528988 5528988 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:5528988C>A c.1801G>T c.(1801-1803)Gat>Tat p.D601Y READ 11 5529738 5529738 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:5529738C>T c.1051G>A c.(1051-1053)Gag>Aag p.E351K READ 11 5530318 5530318 + Silent SNP C C A TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chr11:5530318C>A c.471G>T c.(469-471)ctG>ctT p.L157L READ 11 5530440 5530440 + Missense_Mutation SNP G G C TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr11:5530440G>C c.349C>G c.(349-351)Ctc>Gtc p.L117V READ 11 5530484 5530484 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:5530484C>T c.305G>A c.(304-306)tGc>tAc p.C102Y SARC 11 5529535 5529535 + Silent SNP C C T TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr11:5529535C>T c.1254G>A c.(1252-1254)gaG>gaA p.E418E SARC 11 5529648 5529648 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:5529648G>A c.1141C>T c.(1141-1143)Ccc>Tcc p.P381S SKCM 11 5528910 5528910 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:5528910C>T c.1879G>A c.(1879-1881)Ggc>Agc p.G627S SKCM 11 5529119 5529119 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr11:5529119C>T c.1670G>A c.(1669-1671)gGa>gAa p.G557E SKCM 11 5529150 5529150 + Missense_Mutation SNP G G A TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr11:5529150G>A c.1639C>T c.(1639-1641)Cct>Tct p.P547S SKCM 11 5529171 5529171 + Missense_Mutation SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr11:5529171G>A c.1618C>T c.(1618-1620)Cgc>Tgc p.R540C SKCM 11 5529180 5529180 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr11:5529180C>T c.1609G>A c.(1609-1611)Gaa>Aaa p.E537K SKCM 11 5529328 5529328 + Missense_Mutation SNP C C G TCGA-D3-A3BZ-06A-12D-A196-08 TCGA-D3-A3BZ-10A-01D-A198-08 g.chr11:5529328C>G c.1461G>C c.(1459-1461)agG>agC p.R487S SKCM 11 5529376 5529376 + Silent SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr11:5529376G>A c.1413C>T c.(1411-1413)atC>atT p.I471I SKCM 11 5529400 5529400 + Silent SNP G G A TCGA-D3-A3C6-06A-12D-A196-08 TCGA-D3-A3C6-10A-01D-A198-08 g.chr11:5529400G>A c.1389C>T c.(1387-1389)tcC>tcT p.S463S SKCM 11 5529428 5529428 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr11:5529428C>T c.1361G>A c.(1360-1362)aGg>aAg p.R454K SKCM 11 5529451 5529451 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:5529451C>T c.1338G>A c.(1336-1338)tcG>tcA p.S446S SKCM 11 5529462 5529462 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:5529462C>T c.1327G>A c.(1327-1329)Gat>Aat p.D443N SKCM 11 5529468 5529468 + Silent SNP A A G TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr11:5529468A>G c.1321T>C c.(1321-1323)Ttg>Ctg p.L441L SKCM 11 5529496 5529496 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:5529496C>T c.1293G>A c.(1291-1293)ggG>ggA p.G431G SKCM 11 5529560 5529560 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr11:5529560G>A c.1229C>T c.(1228-1230)cCa>cTa p.P410L SKCM 11 5529598 5529598 + Silent SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr11:5529598G>A c.1191C>T c.(1189-1191)ccC>ccT p.P397P SKCM 11 5529600 5529600 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr11:5529600G>A c.1189C>T c.(1189-1191)Ccc>Tcc p.P397S SKCM 11 5529638 5529638 + Missense_Mutation SNP G G A TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr11:5529638G>A c.1151C>T c.(1150-1152)tCa>tTa p.S384L SKCM 11 5529680 5529680 + Missense_Mutation SNP C C T TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:5529680C>T c.1109G>A c.(1108-1110)aGc>aAc p.S370N SKCM 11 5529719 5529719 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:5529719C>T c.1070G>A c.(1069-1071)gGa>gAa p.G357E SKCM 11 5529724 5529724 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr11:5529724G>A c.1065C>T c.(1063-1065)tcC>tcT p.S355S SKCM 11 5529732 5529732 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:5529732G>A c.1057C>T c.(1057-1059)Ccc>Tcc p.P353S SKCM 11 5529751 5529751 + Silent SNP G G A TCGA-ER-A2NH-06A-11D-A196-08 TCGA-ER-A2NH-10A-01D-A198-08 g.chr11:5529751G>A c.1038C>T c.(1036-1038)ctC>ctT p.L346L SKCM 11 5529823 5529823 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr11:5529823C>T c.966G>A c.(964-966)ggG>ggA p.G322G SKCM 11 5529829 5529829 + Silent SNP C C T TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr11:5529829C>T c.960G>A c.(958-960)caG>caA p.Q320Q SKCM 11 5529837 5529837 + Missense_Mutation SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr11:5529837C>T c.952G>A c.(952-954)Gga>Aga p.G318R SKCM 11 5530011 5530011 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr11:5530011C>T c.778G>A c.(778-780)Gat>Aat p.D260N SKCM 11 5530056 5530056 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr11:5530056C>T c.733G>A c.(733-735)Gag>Aag p.E245K SKCM 11 5530148 5530148 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:5530148G>A c.641C>T c.(640-642)cCg>cTg p.P214L SKCM 11 5530191 5530191 + Silent SNP G G A TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr11:5530191G>A c.598C>T c.(598-600)Ctg>Ttg p.L200L SKCM 11 5530321 5530321 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr11:5530321G>A c.468C>T c.(466-468)tcC>tcT p.S156S SKCM 11 5530396 5530396 + Silent SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr11:5530396G>A c.393C>T c.(391-393)gcC>gcT p.A131A SKCM 11 5530463 5530463 + Missense_Mutation SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr11:5530463G>A c.326C>T c.(325-327)aCc>aTc p.T109I SKCM 11 5530614 5530614 + Missense_Mutation SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr11:5530614C>T c.175G>A c.(175-177)Gat>Aat p.D59N SKCM 11 5530692 5530692 + Missense_Mutation SNP C C T TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr11:5530692C>T c.97G>A c.(97-99)Gag>Aag p.E33K

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 5530579 5530579 single base substitution G C synonymous_variant L70L 210C>G BLCA-US 11 5530516 5530516 single base substitution G A synonymous_variant I91I 273C>T BOCA-FR 11 5527552 5527552 single base substitution A G downstream_gene_variant BRCA-EU 11 5523713 5523713 single base substitution C A downstream_gene_variant BRCA-EU 11 5524677 5524677 single base substitution G A downstream_gene_variant BRCA-EU 11 5526726 5526726 single base substitution C T downstream_gene_variant BRCA-EU 11 5528940 5528940 single base substitution G A downstream_gene_variant BRCA-EU 11 5528940 5528940 single base substitution G A stop_gained Q617* 1849C>T BRCA-EU 11 5529513 5529513 single base substitution C A downstream_gene_variant BRCA-EU 11 5529513 5529513 single base substitution C A missense_variant D426Y 1276G>T BRCA-EU 11 5530544 5530544 single base substitution C T missense_variant R82Q 245G>A BRCA-EU 11 5531236 5531236 single base substitution G A upstream_gene_variant BRCA-EU 11 5531596 5531596 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 5531968 5531968 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 5532950 5532950 single base substitution G T upstream_gene_variant BRCA-EU 11 5533755 5533755 single base substitution C T upstream_gene_variant BRCA-EU 11 5534385 5534385 single base substitution C T upstream_gene_variant BRCA-EU 11 5534791 5534791 single base substitution C G upstream_gene_variant BRCA-EU 11 5535373 5535373 single base substitution G A upstream_gene_variant BRCA-EU 11 5535576 5535576 single base substitution A G upstream_gene_variant BRCA-EU 11 5535580 5535580 single base substitution T C upstream_gene_variant BRCA-EU 11 5535941 5535941 single base substitution C T upstream_gene_variant BRCA-FR 11 5524677 5524677 single base substitution G A downstream_gene_variant BRCA-FR 11 5532950 5532950 single base substitution G T upstream_gene_variant BRCA-FR 11 5534791 5534791 single base substitution C G upstream_gene_variant BRCA-FR 11 5535373 5535373 single base substitution G A upstream_gene_variant BRCA-UK 11 5529333 5529333 single base substitution G A downstream_gene_variant BRCA-UK 11 5529333 5529333 single base substitution G A synonymous_variant L486L 1456C>T BRCA-US 11 5529582 5529582 single base substitution T G downstream_gene_variant BRCA-US 11 5529582 5529582 single base substitution T G missense_variant I403L 1207A>C BRCA-US 11 5529922 5529922 single base substitution G A downstream_gene_variant BRCA-US 11 5529922 5529922 single base substitution G A synonymous_variant T289T 867C>T BRCA-US 11 5530467 5530467 single base substitution G A missense_variant P108S 322C>T BTCA-JP 11 5529134 5529134 single base substitution G A downstream_gene_variant BTCA-JP 11 5529134 5529134 single base substitution G A missense_variant T552M 1655C>T BTCA-JP 11 5529163 5529163 single base substitution T A downstream_gene_variant BTCA-JP 11 5529163 5529163 single base substitution T A synonymous_variant L542L 1626A>T BTCA-JP 11 5529285 5529285 single base substitution G T downstream_gene_variant BTCA-JP 11 5529285 5529285 single base substitution G T missense_variant Q502K 1504C>A BTCA-JP 11 5530148 5530148 single base substitution G A missense_variant P214L 641C>T BTCA-JP 11 5530227 5530227 single base substitution G A missense_variant R188C 562C>T BTCA-JP 11 5530631 5530631 single base substitution C T missense_variant R53H 158G>A BTCA-JP 11 5530730 5530730 single base substitution T A missense_variant H20L 59A>T CESC-US 11 5529679 5529679 single base substitution G A downstream_gene_variant CESC-US 11 5529679 5529679 single base substitution G A synonymous_variant S370S 1110C>T CESC-US 11 5529891 5529891 single base substitution C G downstream_gene_variant CESC-US 11 5529891 5529891 single base substitution C G missense_variant D300H 898G>C CLLE-ES 11 5532756 5532756 single base substitution C A upstream_gene_variant COAD-US 11 5528918 5528918 single base substitution C T downstream_gene_variant COAD-US 11 5528918 5528918 single base substitution C T missense_variant R624Q 1871G>A COAD-US 11 5528925 5528925 single base substitution G T downstream_gene_variant COAD-US 11 5528925 5528925 single base substitution G T missense_variant Q622K 1864C>A COAD-US 11 5528951 5528951 single base substitution T C downstream_gene_variant COAD-US 11 5528951 5528951 single base substitution T C missense_variant E613G 1838A>G COAD-US 11 5529139 5529139 single base substitution T C downstream_gene_variant COAD-US 11 5529139 5529139 single base substitution T C synonymous_variant A550A 1650A>G COAD-US 11 5529314 5529314 single base substitution T C downstream_gene_variant COAD-US 11 5529314 5529314 single base substitution T C missense_variant N492S 1475A>G COAD-US 11 5529332 5529332 single base substitution A G downstream_gene_variant COAD-US 11 5529332 5529332 single base substitution A G missense_variant L486P 1457T>C COAD-US 11 5529384 5529384 single base substitution G A downstream_gene_variant COAD-US 11 5529384 5529384 single base substitution G A missense_variant P469S 1405C>T COAD-US 11 5529594 5529594 single base substitution C T downstream_gene_variant COAD-US 11 5529594 5529594 single base substitution C T missense_variant E399K 1195G>A COAD-US 11 5529961 5529961 single base substitution A G downstream_gene_variant COAD-US 11 5529961 5529961 single base substitution A G synonymous_variant N276N 828T>C COAD-US 11 5529987 5529987 single base substitution C T downstream_gene_variant COAD-US 11 5529987 5529987 single base substitution C T missense_variant A268T 802G>A COAD-US 11 5530135 5530135 single base substitution C T synonymous_variant R218R 654G>A COAD-US 11 5530400 5530400 deletion of <=200bp G - frameshift_variant P130 COAD-US 11 5530615 5530615 single base substitution G A synonymous_variant P58P 174C>T COAD-US 11 5530651 5530651 single base substitution C A synonymous_variant L46L 138G>T COCA-CN 11 5528804 5528804 single base substitution T C 3_prime_UTR_variant COCA-CN 11 5528804 5528804 single base substitution T C downstream_gene_variant COCA-CN 11 5529215 5529215 single base substitution C T downstream_gene_variant COCA-CN 11 5529215 5529215 single base substitution C T missense_variant R525Q 1574G>A COCA-CN 11 5529791 5529791 single base substitution A G downstream_gene_variant COCA-CN 11 5529791 5529791 single base substitution A G missense_variant F333S 998T>C ESAD-UK 11 5523568 5523568 single base substitution T C downstream_gene_variant ESAD-UK 11 5523777 5523777 single base substitution C G downstream_gene_variant ESAD-UK 11 5524013 5524013 single base substitution T A downstream_gene_variant ESAD-UK 11 5524052 5524052 single base substitution A C downstream_gene_variant ESAD-UK 11 5524063 5524063 single base substitution A C downstream_gene_variant ESAD-UK 11 5525110 5525110 single base substitution A G downstream_gene_variant ESAD-UK 11 5525445 5525445 single base substitution A C downstream_gene_variant ESAD-UK 11 5525589 5525589 single base substitution T C downstream_gene_variant ESAD-UK 11 5525792 5525792 single base substitution T A downstream_gene_variant ESAD-UK 11 5525862 5525862 single base substitution A G downstream_gene_variant ESAD-UK 11 5526177 5526177 single base substitution A C downstream_gene_variant ESAD-UK 11 5526497 5526497 single base substitution T G downstream_gene_variant ESAD-UK 11 5526875 5526875 deletion of <=200bp A - downstream_gene_variant ESAD-UK 11 5526881 5526881 single base substitution A G downstream_gene_variant ESAD-UK 11 5527307 5527307 single base substitution C A downstream_gene_variant ESAD-UK 11 5527331 5527331 single base substitution T C downstream_gene_variant ESAD-UK 11 5527357 5527357 single base substitution C T downstream_gene_variant ESAD-UK 11 5527403 5527403 single base substitution A G downstream_gene_variant ESAD-UK 11 5527569 5527569 single base substitution A C downstream_gene_variant ESAD-UK 11 5527667 5527667 single base substitution C A downstream_gene_variant ESAD-UK 11 5527789 5527789 single base substitution T G downstream_gene_variant ESAD-UK 11 5527842 5527842 deletion of <=200bp T - downstream_gene_variant ESAD-UK 11 5528012 5528012 single base substitution G A downstream_gene_variant ESAD-UK 11 5528088 5528088 single base substitution G A downstream_gene_variant ESAD-UK 11 5528181 5528181 single base substitution C T downstream_gene_variant ESAD-UK 11 5528187 5528187 deletion of <=200bp G - downstream_gene_variant ESAD-UK 11 5528649 5528649 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 5528649 5528649 single base substitution T G downstream_gene_variant ESAD-UK 11 5528708 5528708 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 5528708 5528708 single base substitution T G downstream_gene_variant ESAD-UK 11 5529223 5529223 single base substitution T G downstream_gene_variant ESAD-UK 11 5529223 5529223 single base substitution T G missense_variant Q522H 1566A>C ESAD-UK 11 5529999 5529999 single base substitution G C downstream_gene_variant ESAD-UK 11 5529999 5529999 single base substitution G C missense_variant P264A 790C>G ESAD-UK 11 5530138 5530138 single base substitution C A missense_variant M217I 651G>T ESAD-UK 11 5530379 5530379 single base substitution A G missense_variant L137P 410T>C ESAD-UK 11 5530614 5530614 single base substitution C A missense_variant D59Y 175G>T ESAD-UK 11 5530631 5530631 single base substitution C T missense_variant R53H 158G>A ESAD-UK 11 5530778 5530778 single base substitution C A missense_variant G4V 11G>T ESAD-UK 11 5530933 5530933 single base substitution G A intron_variant ESAD-UK 11 5531052 5531052 single base substitution G T intron_variant ESAD-UK 11 5531342 5531342 single base substitution A C upstream_gene_variant ESAD-UK 11 5531446 5531446 single base substitution T G upstream_gene_variant ESAD-UK 11 5531560 5531560 single base substitution T G upstream_gene_variant ESAD-UK 11 5531998 5531998 single base substitution A C upstream_gene_variant ESAD-UK 11 5532533 5532533 single base substitution A C upstream_gene_variant ESAD-UK 11 5532826 5532826 single base substitution G A upstream_gene_variant ESAD-UK 11 5533071 5533071 single base substitution A C upstream_gene_variant ESAD-UK 11 5533401 5533401 single base substitution G A upstream_gene_variant ESAD-UK 11 5533404 5533404 single base substitution T G upstream_gene_variant ESAD-UK 11 5533576 5533576 single base substitution C T upstream_gene_variant ESAD-UK 11 5534190 5534190 single base substitution A C upstream_gene_variant ESAD-UK 11 5534347 5534347 single base substitution T G upstream_gene_variant ESAD-UK 11 5535170 5535170 single base substitution A G upstream_gene_variant ESAD-UK 11 5535177 5535177 single base substitution C A upstream_gene_variant ESAD-UK 11 5535362 5535362 single base substitution T G upstream_gene_variant ESAD-UK 11 5535586 5535586 single base substitution T C upstream_gene_variant ESAD-UK 11 5535749 5535749 single base substitution G A upstream_gene_variant ESCA-CN 11 5529081 5529081 single base substitution C T downstream_gene_variant ESCA-CN 11 5529081 5529081 single base substitution C T missense_variant D570N 1708G>A GBM-US 11 5529018 5529018 single base substitution G A downstream_gene_variant GBM-US 11 5529018 5529018 single base substitution G A missense_variant L591F 1771C>T GBM-US 11 5529360 5529360 single base substitution G A downstream_gene_variant GBM-US 11 5529360 5529360 single base substitution G A synonymous_variant L477L 1429C>T GBM-US 11 5529867 5529867 single base substitution A T downstream_gene_variant GBM-US 11 5529867 5529867 single base substitution A T missense_variant S308T 922T>A GBM-US 11 5529918 5529920 deletion of <=200bp TGG - disruptive_inframe_deletion TS290S GBM-US 11 5529918 5529920 deletion of <=200bp TGG - downstream_gene_variant KIRC-US 11 5528857 5528857 single base substitution G A downstream_gene_variant KIRC-US 11 5528857 5528857 single base substitution G A synonymous_variant D644D 1932C>T LGG-US 11 5530632 5530632 single base substitution G A missense_variant R53C 157C>T LICA-CN 11 5529331 5529331 single base substitution C G downstream_gene_variant LICA-CN 11 5529331 5529331 single base substitution C G synonymous_variant L486L 1458G>C LICA-FR 11 5525159 5525159 single base substitution G C downstream_gene_variant LICA-FR 11 5528962 5528962 single base substitution C T downstream_gene_variant LICA-FR 11 5528962 5528962 single base substitution C T synonymous_variant Q609Q 1827G>A LICA-FR 11 5529613 5529613 single base substitution T C downstream_gene_variant LICA-FR 11 5529613 5529613 single base substitution T C synonymous_variant S392S 1176A>G LICA-FR 11 5529900 5529900 single base substitution C G downstream_gene_variant LICA-FR 11 5529900 5529900 single base substitution C G missense_variant E297Q 889G>C LICA-FR 11 5530045 5530045 single base substitution A T downstream_gene_variant LICA-FR 11 5530045 5530045 single base substitution A T synonymous_variant P248P 744T>A LICA-FR 11 5530111 5530111 single base substitution G A downstream_gene_variant LICA-FR 11 5530111 5530111 single base substitution G A synonymous_variant N226N 678C>T LICA-FR 11 5535948 5535948 single base substitution T C upstream_gene_variant LIHC-US 11 5528949 5528949 single base substitution C G downstream_gene_variant LIHC-US 11 5528949 5528949 single base substitution C G missense_variant A614P 1840G>C LIHC-US 11 5529136 5529136 single base substitution C A downstream_gene_variant LIHC-US 11 5529136 5529136 single base substitution C A synonymous_variant G551G 1653G>T LIHC-US 11 5530137 5530137 single base substitution G A missense_variant R218W 652C>T LINC-JP 11 5526589 5526589 single base substitution C T downstream_gene_variant LINC-JP 11 5528286 5528286 single base substitution C T downstream_gene_variant LINC-JP 11 5528597 5528597 single base substitution C A 3_prime_UTR_variant LINC-JP 11 5528597 5528597 single base substitution C A downstream_gene_variant LINC-JP 11 5528598 5528598 single base substitution C G 3_prime_UTR_variant LINC-JP 11 5528598 5528598 single base substitution C G downstream_gene_variant LINC-JP 11 5528861 5528861 insertion of <=200bp - C downstream_gene_variant LINC-JP 11 5528861 5528861 insertion of <=200bp - C frameshift_variant G643G? LINC-JP 11 5529113 5529113 single base substitution A G downstream_gene_variant LINC-JP 11 5529113 5529113 single base substitution A G missense_variant I559T 1676T>C LINC-JP 11 5530170 5530170 single base substitution T A missense_variant I207F 619A>T LINC-JP 11 5530400 5530400 single base substitution G A missense_variant P130L 389C>T LIRI-JP 11 5526677 5526677 single base substitution T C downstream_gene_variant LIRI-JP 11 5528982 5528982 single base substitution C G downstream_gene_variant LIRI-JP 11 5528982 5528982 single base substitution C G missense_variant V603L 1807G>C LIRI-JP 11 5529611 5529611 single base substitution C A downstream_gene_variant LIRI-JP 11 5529611 5529611 single base substitution C A missense_variant G393V 1178G>T LIRI-JP 11 5530430 5530430 single base substitution G A missense_variant P120L 359C>T LIRI-JP 11 5531141 5531141 single base substitution C T 5_prime_UTR_variant LIRI-JP 11 5531292 5531292 single base substitution T A upstream_gene_variant LIRI-JP 11 5532060 5532060 single base substitution G C upstream_gene_variant LIRI-JP 11 5534319 5534319 single base substitution T A upstream_gene_variant LIRI-JP 11 5534755 5534755 single base substitution T C upstream_gene_variant LIRI-JP 11 5535122 5535122 single base substitution C T upstream_gene_variant LIRI-JP 11 5535470 5535470 single base substitution T C upstream_gene_variant LIRI-JP 11 5535505 5535505 single base substitution T C upstream_gene_variant LUSC-KR 11 5524947 5524947 single base substitution T C downstream_gene_variant LUSC-KR 11 5527028 5527028 single base substitution A C downstream_gene_variant LUSC-KR 11 5528918 5528918 single base substitution C T downstream_gene_variant LUSC-KR 11 5528918 5528918 single base substitution C T missense_variant R624Q 1871G>A LUSC-KR 11 5529139 5529139 single base substitution T C downstream_gene_variant LUSC-KR 11 5529139 5529139 single base substitution T C synonymous_variant A550A 1650A>G LUSC-KR 11 5529192 5529192 single base substitution C T downstream_gene_variant LUSC-KR 11 5529192 5529192 single base substitution C T missense_variant V533I 1597G>A LUSC-KR 11 5529920 5529920 single base substitution G C downstream_gene_variant LUSC-KR 11 5529920 5529920 single base substitution G C missense_variant T290S 869C>G LUSC-KR 11 5533354 5533354 single base substitution C A upstream_gene_variant LUSC-KR 11 5533858 5533858 single base substitution G T upstream_gene_variant LUSC-US 11 5529151 5529151 single base substitution C T downstream_gene_variant LUSC-US 11 5529151 5529151 single base substitution C T missense_variant M546I 1638G>A LUSC-US 11 5529258 5529258 single base substitution G A downstream_gene_variant LUSC-US 11 5529258 5529258 single base substitution G A missense_variant L511F 1531C>T LUSC-US 11 5529375 5529375 single base substitution G T downstream_gene_variant LUSC-US 11 5529375 5529375 single base substitution G T missense_variant P472T 1414C>A LUSC-US 11 5529644 5529644 deletion of <=200bp G - downstream_gene_variant LUSC-US 11 5529644 5529644 deletion of <=200bp G - frameshift_variant P382 LUSC-US 11 5530016 5530016 single base substitution T C downstream_gene_variant LUSC-US 11 5530016 5530016 single base substitution T C missense_variant Y258C 773A>G LUSC-US 11 5530073 5530073 single base substitution C A downstream_gene_variant LUSC-US 11 5530073 5530073 single base substitution C A missense_variant R239L 716G>T LUSC-US 11 5530093 5530093 single base substitution C A downstream_gene_variant LUSC-US 11 5530093 5530093 single base substitution C A missense_variant E232D 696G>T LUSC-US 11 5530345 5530345 single base substitution A G synonymous_variant R148R 444T>C MALY-DE 11 5523823 5523831 deletion of <=200bp ATAGAAGTG - downstream_gene_variant MALY-DE 11 5525168 5525168 single base substitution C T downstream_gene_variant MALY-DE 11 5526374 5526374 single base substitution C G downstream_gene_variant MALY-DE 11 5526402 5526402 single base substitution A G downstream_gene_variant MELA-AU 11 5523534 5523534 single base substitution C T downstream_gene_variant MELA-AU 11 5523582 5523582 single base substitution C T downstream_gene_variant MELA-AU 11 5523594 5523594 single base substitution C T downstream_gene_variant MELA-AU 11 5523713 5523713 single base substitution C T downstream_gene_variant MELA-AU 11 5524073 5524073 single base substitution G A downstream_gene_variant MELA-AU 11 5524148 5524148 single base substitution C T downstream_gene_variant MELA-AU 11 5524228 5524228 single base substitution G A downstream_gene_variant MELA-AU 11 5524229 5524229 single base substitution G A downstream_gene_variant MELA-AU 11 5524230 5524230 insertion of <=200bp - A downstream_gene_variant MELA-AU 11 5524363 5524363 single base substitution C T downstream_gene_variant MELA-AU 11 5524524 5524524 single base substitution G A downstream_gene_variant MELA-AU 11 5524545 5524545 single base substitution C T downstream_gene_variant MELA-AU 11 5524677 5524677 single base substitution G A downstream_gene_variant MELA-AU 11 5524685 5524685 single base substitution C T downstream_gene_variant MELA-AU 11 5524699 5524699 single base substitution G A downstream_gene_variant MELA-AU 11 5524734 5524734 single base substitution C T downstream_gene_variant MELA-AU 11 5524779 5524779 single base substitution G A downstream_gene_variant MELA-AU 11 5524880 5524880 single base substitution C T downstream_gene_variant MELA-AU 11 5524997 5524997 single base substitution C T downstream_gene_variant MELA-AU 11 5525256 5525256 single base substitution A T downstream_gene_variant MELA-AU 11 5525268 5525268 single base substitution C T downstream_gene_variant MELA-AU 11 5525614 5525614 single base substitution C T downstream_gene_variant MELA-AU 11 5525708 5525708 single base substitution C T downstream_gene_variant MELA-AU 11 5525814 5525814 single base substitution G A downstream_gene_variant MELA-AU 11 5525881 5525881 single base substitution C T downstream_gene_variant MELA-AU 11 5526076 5526076 single base substitution G A downstream_gene_variant MELA-AU 11 5526113 5526113 single base substitution G A downstream_gene_variant MELA-AU 11 5526138 5526138 single base substitution C T downstream_gene_variant MELA-AU 11 5526151 5526151 single base substitution G A downstream_gene_variant MELA-AU 11 5526246 5526246 single base substitution C T downstream_gene_variant MELA-AU 11 5526288 5526288 single base substitution C T downstream_gene_variant MELA-AU 11 5526301 5526301 single base substitution G A downstream_gene_variant MELA-AU 11 5526373 5526373 single base substitution C T downstream_gene_variant MELA-AU 11 5526495 5526495 single base substitution C T downstream_gene_variant MELA-AU 11 5526550 5526550 single base substitution C T downstream_gene_variant MELA-AU 11 5526603 5526603 single base substitution G A downstream_gene_variant MELA-AU 11 5526640 5526640 single base substitution C A downstream_gene_variant MELA-AU 11 5526803 5526803 single base substitution C T downstream_gene_variant MELA-AU 11 5526854 5526854 single base substitution C T downstream_gene_variant MELA-AU 11 5526947 5526947 single base substitution G A downstream_gene_variant MELA-AU 11 5526985 5526985 single base substitution C T downstream_gene_variant MELA-AU 11 5527018 5527018 single base substitution G A downstream_gene_variant MELA-AU 11 5527059 5527059 single base substitution G A downstream_gene_variant MELA-AU 11 5527136 5527136 single base substitution G A downstream_gene_variant MELA-AU 11 5527222 5527222 single base substitution C T downstream_gene_variant MELA-AU 11 5527479 5527479 single base substitution A T downstream_gene_variant MELA-AU 11 5527512 5527512 single base substitution G A downstream_gene_variant MELA-AU 11 5527583 5527583 single base substitution G A downstream_gene_variant MELA-AU 11 5527609 5527609 single base substitution G A downstream_gene_variant MELA-AU 11 5527626 5527626 single base substitution C T downstream_gene_variant MELA-AU 11 5527793 5527793 single base substitution C T downstream_gene_variant MELA-AU 11 5527982 5527982 single base substitution C T downstream_gene_variant MELA-AU 11 5528167 5528167 single base substitution C T downstream_gene_variant MELA-AU 11 5528236 5528236 single base substitution C T downstream_gene_variant MELA-AU 11 5528490 5528490 single base substitution C T downstream_gene_variant MELA-AU 11 5528503 5528503 single base substitution C T downstream_gene_variant MELA-AU 11 5528627 5528627 single base substitution C T 3_prime_UTR_variant MELA-AU 11 5528627 5528627 single base substitution C T downstream_gene_variant MELA-AU 11 5528663 5528663 single base substitution C T 3_prime_UTR_variant MELA-AU 11 5528663 5528663 single base substitution C T downstream_gene_variant MELA-AU 11 5528769 5528769 single base substitution G A 3_prime_UTR_variant MELA-AU 11 5528769 5528769 single base substitution G A downstream_gene_variant MELA-AU 11 5528776 5528776 single base substitution G A 3_prime_UTR_variant MELA-AU 11 5528776 5528776 single base substitution G A downstream_gene_variant MELA-AU 11 5528946 5528946 single base substitution G A downstream_gene_variant MELA-AU 11 5528946 5528946 single base substitution G A missense_variant H615Y 1843C>T MELA-AU 11 5529078 5529078 single base substitution G A downstream_gene_variant MELA-AU 11 5529078 5529078 single base substitution G A missense_variant P571S 1711C>T MELA-AU 11 5529150 5529150 single base substitution G A downstream_gene_variant MELA-AU 11 5529150 5529150 single base substitution G A missense_variant P547S 1639C>T MELA-AU 11 5529221 5529221 single base substitution G A downstream_gene_variant MELA-AU 11 5529221 5529221 single base substitution G A missense_variant A523V 1568C>T MELA-AU 11 5529496 5529496 single base substitution C T downstream_gene_variant MELA-AU 11 5529496 5529496 single base substitution C T synonymous_variant G431G 1293G>A MELA-AU 11 5529562 5529562 single base substitution G A downstream_gene_variant MELA-AU 11 5529562 5529562 single base substitution G A synonymous_variant C409C 1227C>T MELA-AU 11 5529601 5529601 single base substitution G A downstream_gene_variant MELA-AU 11 5529601 5529601 single base substitution G A synonymous_variant L396L 1188C>T MELA-AU 11 5529784 5529784 single base substitution G A downstream_gene_variant MELA-AU 11 5529784 5529784 single base substitution G A synonymous_variant N335N 1005C>T MELA-AU 11 5529824 5529824 single base substitution C T downstream_gene_variant MELA-AU 11 5529824 5529824 single base substitution C T missense_variant G322E 965G>A MELA-AU 11 5529836 5529836 single base substitution C T downstream_gene_variant MELA-AU 11 5529836 5529836 single base substitution C T missense_variant G318E 953G>A MELA-AU 11 5529911 5529911 single base substitution G A downstream_gene_variant MELA-AU 11 5529911 5529911 single base substitution G A missense_variant P293L 878C>T MELA-AU 11 5530011 5530011 single base substitution C T downstream_gene_variant MELA-AU 11 5530011 5530011 single base substitution C T missense_variant D260N 778G>A MELA-AU 11 5530011 5530012 multiple base substitution (>=2bp and <=200bp) CT TC downstream_gene_variant MELA-AU 11 5530011 5530012 multiple base substitution (>=2bp and <=200bp) CT TC missense_variant TD259TN MELA-AU 11 5530090 5530090 single base substitution C T downstream_gene_variant MELA-AU 11 5530090 5530090 single base substitution C T missense_variant M233I 699G>A MELA-AU 11 5530175 5530175 single base substitution G A missense_variant P205L 614C>T MELA-AU 11 5530186 5530186 single base substitution G A synonymous_variant I201I 603C>T MELA-AU 11 5530256 5530256 single base substitution G A missense_variant P178L 533C>T MELA-AU 11 5530367 5530367 single base substitution C T missense_variant S141N 422G>A MELA-AU 11 5530575 5530575 single base substitution C T missense_variant D72N 214G>A MELA-AU 11 5530614 5530614 single base substitution C T missense_variant D59N 175G>A MELA-AU 11 5530648 5530648 single base substitution C T synonymous_variant K47K 141G>A MELA-AU 11 5530734 5530734 single base substitution G A missense_variant P19S 55C>T MELA-AU 11 5530843 5530843 single base substitution G A 5_prime_UTR_variant MELA-AU 11 5530843 5530843 single base substitution G A intron_variant MELA-AU 11 5530858 5530858 single base substitution C T intron_variant MELA-AU 11 5530858 5530858 single base substitution C T splice_acceptor_variant MELA-AU 11 5530888 5530888 single base substitution G A intron_variant MELA-AU 11 5530894 5530894 single base substitution G A intron_variant MELA-AU 11 5530921 5530921 single base substitution G A intron_variant MELA-AU 11 5530941 5530941 single base substitution G A intron_variant MELA-AU 11 5531011 5531011 single base substitution G A intron_variant MELA-AU 11 5531078 5531078 single base substitution G A intron_variant MELA-AU 11 5531085 5531085 single base substitution C T intron_variant MELA-AU 11 5531149 5531149 single base substitution C T 5_prime_UTR_variant MELA-AU 11 5531212 5531212 single base substitution C T 5_prime_UTR_variant MELA-AU 11 5531212 5531212 single base substitution C T upstream_gene_variant MELA-AU 11 5531214 5531214 single base substitution C T 5_prime_UTR_variant MELA-AU 11 5531214 5531214 single base substitution C T upstream_gene_variant MELA-AU 11 5531331 5531331 single base substitution C T upstream_gene_variant MELA-AU 11 5531437 5531437 single base substitution T A upstream_gene_variant MELA-AU 11 5531448 5531448 single base substitution C T upstream_gene_variant MELA-AU 11 5531514 5531514 single base substitution G A upstream_gene_variant MELA-AU 11 5531545 5531545 single base substitution C T upstream_gene_variant MELA-AU 11 5531555 5531555 single base substitution T C upstream_gene_variant MELA-AU 11 5531558 5531558 single base substitution G A upstream_gene_variant MELA-AU 11 5531576 5531576 single base substitution G A upstream_gene_variant MELA-AU 11 5531598 5531598 single base substitution T C upstream_gene_variant MELA-AU 11 5531628 5531628 single base substitution C T upstream_gene_variant MELA-AU 11 5531750 5531750 single base substitution G A upstream_gene_variant MELA-AU 11 5531779 5531779 single base substitution A G upstream_gene_variant MELA-AU 11 5531782 5531782 single base substitution C T upstream_gene_variant MELA-AU 11 5531974 5531974 single base substitution A G upstream_gene_variant MELA-AU 11 5531977 5531977 single base substitution G A upstream_gene_variant MELA-AU 11 5531995 5531995 single base substitution C T upstream_gene_variant MELA-AU 11 5532000 5532000 single base substitution G A upstream_gene_variant MELA-AU 11 5532006 5532006 single base substitution G T upstream_gene_variant MELA-AU 11 5532012 5532012 single base substitution C T upstream_gene_variant MELA-AU 11 5532104 5532104 single base substitution G A upstream_gene_variant MELA-AU 11 5532164 5532164 single base substitution G A upstream_gene_variant MELA-AU 11 5532283 5532283 single base substitution C T upstream_gene_variant MELA-AU 11 5532327 5532327 single base substitution C T upstream_gene_variant MELA-AU 11 5532360 5532360 single base substitution G A upstream_gene_variant MELA-AU 11 5532565 5532565 single base substitution G A upstream_gene_variant MELA-AU 11 5532596 5532596 single base substitution G A upstream_gene_variant MELA-AU 11 5532717 5532717 single base substitution G A upstream_gene_variant MELA-AU 11 5532850 5532850 single base substitution G A upstream_gene_variant MELA-AU 11 5532862 5532862 single base substitution G A upstream_gene_variant MELA-AU 11 5532903 5532903 single base substitution G A upstream_gene_variant MELA-AU 11 5532995 5532995 single base substitution G A upstream_gene_variant MELA-AU 11 5533004 5533004 single base substitution G A upstream_gene_variant MELA-AU 11 5533017 5533017 single base substitution G A upstream_gene_variant MELA-AU 11 5533024 5533024 single base substitution C T upstream_gene_variant MELA-AU 11 5533237 5533237 single base substitution G A upstream_gene_variant MELA-AU 11 5533238 5533238 single base substitution A C upstream_gene_variant MELA-AU 11 5533270 5533270 single base substitution C T upstream_gene_variant MELA-AU 11 5533276 5533276 single base substitution G A upstream_gene_variant MELA-AU 11 5533283 5533283 single base substitution C T upstream_gene_variant MELA-AU 11 5533317 5533317 single base substitution G A upstream_gene_variant MELA-AU 11 5533581 5533581 single base substitution G A upstream_gene_variant MELA-AU 11 5533582 5533582 single base substitution G A upstream_gene_variant MELA-AU 11 5533618 5533618 single base substitution C T upstream_gene_variant MELA-AU 11 5533671 5533671 single base substitution G A upstream_gene_variant MELA-AU 11 5533771 5533771 single base substitution T C upstream_gene_variant MELA-AU 11 5533832 5533832 single base substitution G A upstream_gene_variant MELA-AU 11 5534102 5534102 single base substitution C T upstream_gene_variant MELA-AU 11 5534138 5534138 single base substitution C T upstream_gene_variant MELA-AU 11 5534154 5534154 single base substitution A G upstream_gene_variant MELA-AU 11 5534193 5534193 single base substitution G A upstream_gene_variant MELA-AU 11 5534216 5534216 single base substitution C T upstream_gene_variant MELA-AU 11 5534282 5534283 multiple base substitution (>=2bp and <=200bp) TC GT upstream_gene_variant MELA-AU 11 5534395 5534395 single base substitution C T upstream_gene_variant MELA-AU 11 5534414 5534414 single base substitution C T upstream_gene_variant MELA-AU 11 5534796 5534796 single base substitution C T upstream_gene_variant MELA-AU 11 5534860 5534860 single base substitution G A upstream_gene_variant MELA-AU 11 5534914 5534914 single base substitution G A upstream_gene_variant MELA-AU 11 5534956 5534956 single base substitution G A upstream_gene_variant MELA-AU 11 5535258 5535258 single base substitution C T upstream_gene_variant MELA-AU 11 5535624 5535624 single base substitution C T upstream_gene_variant MELA-AU 11 5535992 5535992 single base substitution C T upstream_gene_variant MELA-AU 11 5536102 5536102 single base substitution G A upstream_gene_variant MELA-AU 11 5536113 5536113 single base substitution G A upstream_gene_variant MELA-AU 11 5536124 5536124 single base substitution G A upstream_gene_variant MELA-AU 11 5536131 5536131 single base substitution A G upstream_gene_variant MELA-AU 11 5536175 5536175 single base substitution G A upstream_gene_variant ORCA-IN 11 5526997 5526997 single base substitution G C downstream_gene_variant OV-AU 11 5527334 5527334 single base substitution C A downstream_gene_variant OV-AU 11 5531619 5531619 single base substitution T C upstream_gene_variant OV-AU 11 5531788 5531788 single base substitution T C upstream_gene_variant OV-AU 11 5532752 5532752 single base substitution G T upstream_gene_variant OV-AU 11 5534744 5534744 single base substitution G A upstream_gene_variant OV-AU 11 5535266 5535266 single base substitution A T upstream_gene_variant OV-US 11 5530137 5530137 single base substitution G A missense_variant R218W 652C>T PACA-AU 11 5526977 5526977 single base substitution G A downstream_gene_variant PACA-AU 11 5528490 5528490 single base substitution C T downstream_gene_variant PACA-AU 11 5529216 5529216 single base substitution G A downstream_gene_variant PACA-AU 11 5529216 5529216 single base substitution G A missense_variant R525W 1573C>T PACA-AU 11 5529644 5529644 single base substitution G T downstream_gene_variant PACA-AU 11 5529644 5529644 single base substitution G T missense_variant P382Q 1145C>A PACA-AU 11 5531672 5531672 single base substitution G A upstream_gene_variant PACA-AU 11 5535511 5535511 single base substitution A T upstream_gene_variant PACA-CA 11 5524588 5524588 single base substitution C A downstream_gene_variant PACA-CA 11 5525832 5525832 single base substitution A T downstream_gene_variant PACA-CA 11 5526734 5526734 single base substitution C T downstream_gene_variant PACA-CA 11 5527984 5527984 single base substitution T G downstream_gene_variant PACA-CA 11 5528260 5528260 single base substitution C T downstream_gene_variant PACA-CA 11 5528796 5528796 single base substitution C T 3_prime_UTR_variant PACA-CA 11 5528796 5528796 single base substitution C T downstream_gene_variant PACA-CA 11 5528819 5528819 single base substitution T C 3_prime_UTR_variant PACA-CA 11 5528819 5528819 single base substitution T C downstream_gene_variant PACA-CA 11 5529265 5529265 single base substitution C A downstream_gene_variant PACA-CA 11 5529265 5529265 single base substitution C A synonymous_variant L508L 1524G>T PACA-CA 11 5530931 5530931 single base substitution G A intron_variant PACA-CA 11 5531028 5531028 single base substitution G C intron_variant PACA-CA 11 5531235 5531235 single base substitution C T upstream_gene_variant PACA-CA 11 5533478 5533480 deletion of <=200bp ATT - upstream_gene_variant PACA-CA 11 5534722 5534722 single base substitution A G upstream_gene_variant PACA-CA 11 5535186 5535186 deletion of <=200bp T - upstream_gene_variant PACA-CA 11 5535625 5535625 single base substitution G A upstream_gene_variant PACA-CA 11 5535811 5535811 single base substitution A G upstream_gene_variant PAEN-AU 11 5530630 5530630 single base substitution G T synonymous_variant R53R 159C>A PRAD-CA 11 5526909 5526909 single base substitution T C downstream_gene_variant PRAD-CA 11 5529071 5529071 single base substitution G T downstream_gene_variant PRAD-CA 11 5529071 5529071 single base substitution G T missense_variant P573Q 1718C>A PRAD-UK 11 5528860 5528860 single base substitution G A downstream_gene_variant PRAD-UK 11 5528860 5528860 single base substitution G A synonymous_variant G643G 1929C>T PRAD-UK 11 5532910 5532910 single base substitution T C upstream_gene_variant PRAD-US 11 5529391 5529391 single base substitution T C downstream_gene_variant PRAD-US 11 5529391 5529391 single base substitution T C synonymous_variant A466A 1398A>G PRAD-US 11 5529918 5529920 deletion of <=200bp TGG - disruptive_inframe_deletion TS290S PRAD-US 11 5529918 5529920 deletion of <=200bp TGG - downstream_gene_variant RECA-EU 11 5529496 5529496 single base substitution C T downstream_gene_variant RECA-EU 11 5529496 5529496 single base substitution C T synonymous_variant G431G 1293G>A SKCA-BR 11 5524240 5524240 single base substitution G A downstream_gene_variant SKCA-BR 11 5525063 5525063 single base substitution G A downstream_gene_variant SKCA-BR 11 5525401 5525401 single base substitution G A downstream_gene_variant SKCA-BR 11 5526186 5526186 single base substitution C T downstream_gene_variant SKCA-BR 11 5526695 5526695 single base substitution G A downstream_gene_variant SKCA-BR 11 5527013 5527013 single base substitution G A downstream_gene_variant SKCA-BR 11 5527516 5527516 single base substitution G A downstream_gene_variant SKCA-BR 11 5527619 5527619 single base substitution G A downstream_gene_variant SKCA-BR 11 5528486 5528486 single base substitution C T downstream_gene_variant SKCA-BR 11 5530614 5530614 single base substitution C T missense_variant D59N 175G>A SKCA-BR 11 5530635 5530635 single base substitution G A stop_gained Q52* 154C>T SKCA-BR 11 5531077 5531077 single base substitution G A intron_variant SKCA-BR 11 5531217 5531217 single base substitution C T upstream_gene_variant SKCA-BR 11 5531286 5531286 single base substitution G A upstream_gene_variant SKCA-BR 11 5531523 5531523 single base substitution A C upstream_gene_variant SKCA-BR 11 5531577 5531577 single base substitution G A upstream_gene_variant SKCA-BR 11 5534719 5534719 single base substitution A C upstream_gene_variant SKCA-BR 11 5534809 5534809 single base substitution G A upstream_gene_variant SKCA-BR 11 5535003 5535003 single base substitution G A upstream_gene_variant SKCA-BR 11 5535750 5535750 single base substitution G A upstream_gene_variant SKCM-US 11 5528910 5528910 single base substitution C T downstream_gene_variant SKCM-US 11 5528910 5528910 single base substitution C T missense_variant G627S 1879G>A SKCM-US 11 5529150 5529150 single base substitution G A downstream_gene_variant SKCM-US 11 5529150 5529150 single base substitution G A missense_variant P547S 1639C>T SKCM-US 11 5529171 5529171 single base substitution G A downstream_gene_variant SKCM-US 11 5529171 5529171 single base substitution G A missense_variant R540C 1618C>T SKCM-US 11 5529180 5529180 single base substitution C T downstream_gene_variant SKCM-US 11 5529180 5529180 single base substitution C T missense_variant E537K 1609G>A SKCM-US 11 5529328 5529328 single base substitution C G downstream_gene_variant SKCM-US 11 5529328 5529328 single base substitution C G missense_variant R487S 1461G>C SKCM-US 11 5529376 5529376 single base substitution G A downstream_gene_variant SKCM-US 11 5529376 5529376 single base substitution G A synonymous_variant I471I 1413C>T SKCM-US 11 5529400 5529400 single base substitution G A downstream_gene_variant SKCM-US 11 5529400 5529400 single base substitution G A synonymous_variant S463S 1389C>T SKCM-US 11 5529428 5529428 single base substitution C T downstream_gene_variant SKCM-US 11 5529428 5529428 single base substitution C T missense_variant R454K 1361G>A SKCM-US 11 5529439 5529439 single base substitution A C downstream_gene_variant SKCM-US 11 5529439 5529439 single base substitution A C missense_variant D450E 1350T>G SKCM-US 11 5529451 5529451 single base substitution C T downstream_gene_variant SKCM-US 11 5529451 5529451 single base substitution C T synonymous_variant S446S 1338G>A SKCM-US 11 5529462 5529462 single base substitution C T downstream_gene_variant SKCM-US 11 5529462 5529462 single base substitution C T missense_variant D443N 1327G>A SKCM-US 11 5529468 5529468 single base substitution A G downstream_gene_variant SKCM-US 11 5529468 5529468 single base substitution A G synonymous_variant L441L 1321T>C SKCM-US 11 5529496 5529496 single base substitution C T downstream_gene_variant SKCM-US 11 5529496 5529496 single base substitution C T synonymous_variant G431G 1293G>A SKCM-US 11 5529560 5529560 single base substitution G A downstream_gene_variant SKCM-US 11 5529560 5529560 single base substitution G A missense_variant P410L 1229C>T SKCM-US 11 5529598 5529598 single base substitution G A downstream_gene_variant SKCM-US 11 5529598 5529598 single base substitution G A synonymous_variant P397P 1191C>T SKCM-US 11 5529600 5529600 single base substitution G A downstream_gene_variant SKCM-US 11 5529600 5529600 single base substitution G A missense_variant P397S 1189C>T SKCM-US 11 5529638 5529638 single base substitution G A downstream_gene_variant SKCM-US 11 5529638 5529638 single base substitution G A missense_variant S384L 1151C>T SKCM-US 11 5529653 5529653 single base substitution C T downstream_gene_variant SKCM-US 11 5529653 5529653 single base substitution C T missense_variant R379K 1136G>A SKCM-US 11 5529680 5529680 single base substitution C T downstream_gene_variant SKCM-US 11 5529680 5529680 single base substitution C T missense_variant S370N 1109G>A SKCM-US 11 5529719 5529719 single base substitution C T downstream_gene_variant SKCM-US 11 5529719 5529719 single base substitution C T missense_variant G357E 1070G>A SKCM-US 11 5529724 5529724 single base substitution G A downstream_gene_variant SKCM-US 11 5529724 5529724 single base substitution G A synonymous_variant S355S 1065C>T SKCM-US 11 5529732 5529732 single base substitution G A downstream_gene_variant SKCM-US 11 5529732 5529732 single base substitution G A missense_variant P353S 1057C>T SKCM-US 11 5529751 5529751 single base substitution G A downstream_gene_variant SKCM-US 11 5529751 5529751 single base substitution G A synonymous_variant L346L 1038C>T SKCM-US 11 5529823 5529823 single base substitution C T downstream_gene_variant SKCM-US 11 5529823 5529823 single base substitution C T synonymous_variant G322G 966G>A SKCM-US 11 5529829 5529829 single base substitution C T downstream_gene_variant SKCM-US 11 5529829 5529829 single base substitution C T synonymous_variant Q320Q 960G>A SKCM-US 11 5529836 5529836 single base substitution C T downstream_gene_variant SKCM-US 11 5529836 5529836 single base substitution C T missense_variant G318E 953G>A SKCM-US 11 5529837 5529837 single base substitution C T downstream_gene_variant SKCM-US 11 5529837 5529837 single base substitution C T missense_variant G318R 952G>A SKCM-US 11 5529918 5529920 deletion of <=200bp TGG - disruptive_inframe_deletion TS290S SKCM-US 11 5529918 5529920 deletion of <=200bp TGG - downstream_gene_variant SKCM-US 11 5530011 5530011 single base substitution C T downstream_gene_variant SKCM-US 11 5530011 5530011 single base substitution C T missense_variant D260N 778G>A SKCM-US 11 5530056 5530056 single base substitution C T downstream_gene_variant SKCM-US 11 5530056 5530056 single base substitution C T missense_variant E245K 733G>A SKCM-US 11 5530148 5530148 single base substitution G A missense_variant P214L 641C>T SKCM-US 11 5530321 5530321 single base substitution G A synonymous_variant S156S 468C>T SKCM-US 11 5530396 5530396 single base substitution G A synonymous_variant A131A 393C>T SKCM-US 11 5530445 5530445 single base substitution C T missense_variant G115E 344G>A SKCM-US 11 5530452 5530452 single base substitution T C missense_variant S113G 337A>G SKCM-US 11 5530463 5530463 single base substitution G A missense_variant T109I 326C>T SKCM-US 11 5530614 5530614 single base substitution C T missense_variant D59N 175G>A SKCM-US 11 5530615 5530615 single base substitution G A synonymous_variant P58P 174C>T SKCM-US 11 5530692 5530692 single base substitution C T missense_variant E33K 97G>A STAD-US 11 5528836 5528836 single base substitution C T downstream_gene_variant STAD-US 11 5528836 5528836 single base substitution C T synonymous_variant K651K 1953G>A STAD-US 11 5528867 5528867 single base substitution G A downstream_gene_variant STAD-US 11 5528867 5528867 single base substitution G A missense_variant T641M 1922C>T STAD-US 11 5528897 5528897 single base substitution C T downstream_gene_variant STAD-US 11 5528897 5528897 single base substitution C T missense_variant R631H 1892G>A STAD-US 11 5528945 5528945 single base substitution T G downstream_gene_variant STAD-US 11 5528945 5528945 single base substitution T G missense_variant H615P 1844A>C STAD-US 11 5529133 5529133 single base substitution C T downstream_gene_variant STAD-US 11 5529133 5529133 single base substitution C T synonymous_variant T552T 1656G>A STAD-US 11 5529220 5529220 single base substitution G C downstream_gene_variant STAD-US 11 5529220 5529220 single base substitution G C synonymous_variant A523A 1569C>G STAD-US 11 5529402 5529402 deletion of <=200bp A - downstream_gene_variant STAD-US 11 5529402 5529402 deletion of <=200bp A - frameshift_variant S463 STAD-US 11 5529402 5529402 single base substitution A G downstream_gene_variant STAD-US 11 5529402 5529402 single base substitution A G missense_variant S463P 1387T>C STAD-US 11 5529610 5529610 single base substitution G A downstream_gene_variant STAD-US 11 5529610 5529610 single base substitution G A synonymous_variant G393G 1179C>T STAD-US 11 5529644 5529644 deletion of <=200bp G - downstream_gene_variant STAD-US 11 5529644 5529644 deletion of <=200bp G - frameshift_variant P382 STAD-US 11 5529729 5529729 deletion of <=200bp G - downstream_gene_variant STAD-US 11 5529729 5529729 deletion of <=200bp G - frameshift_variant Q354 STAD-US 11 5529786 5529786 single base substitution T G downstream_gene_variant STAD-US 11 5529786 5529786 single base substitution T G missense_variant N335H 1003A>C STAD-US 11 5529850 5529850 single base substitution T C downstream_gene_variant STAD-US 11 5529850 5529850 single base substitution T C synonymous_variant S313S 939A>G STAD-US 11 5529962 5529962 single base substitution T G downstream_gene_variant STAD-US 11 5529962 5529962 single base substitution T G missense_variant N276T 827A>C STAD-US 11 5530122 5530122 single base substitution A G downstream_gene_variant STAD-US 11 5530122 5530122 single base substitution A G missense_variant F223L 667T>C STAD-US 11 5530154 5530154 single base substitution T C missense_variant N212S 635A>G STAD-US 11 5530452 5530452 single base substitution T C missense_variant S113G 337A>G THCA-SA 11 5528633 5528633 single base substitution C T 3_prime_UTR_variant THCA-SA 11 5528633 5528633 single base substitution C T downstream_gene_variant THCA-US 11 5528997 5528997 single base substitution T C downstream_gene_variant THCA-US 11 5528997 5528997 single base substitution T C missense_variant M598V 1792A>G THCA-US 11 5530349 5530349 single base substitution T C missense_variant Y147C 440A>G THCA-US 11 5530553 5530553 single base substitution C T missense_variant C79Y 236G>A UCEC-US 11 5528821 5528821 single base substitution C A downstream_gene_variant UCEC-US 11 5528821 5528821 single base substitution C A stop_lost *656Y 1968G>T UCEC-US 11 5529180 5529180 single base substitution C A downstream_gene_variant UCEC-US 11 5529180 5529180 single base substitution C A stop_gained E537* 1609G>T UCEC-US 11 5529304 5529304 single base substitution T C downstream_gene_variant UCEC-US 11 5529304 5529304 single base substitution T C synonymous_variant P495P 1485A>G UCEC-US 11 5529349 5529349 single base substitution C T downstream_gene_variant UCEC-US 11 5529349 5529349 single base substitution C T synonymous_variant P480P 1440G>A UCEC-US 11 5529394 5529394 single base substitution C T downstream_gene_variant UCEC-US 11 5529394 5529394 single base substitution C T synonymous_variant T465T 1395G>A UCEC-US 11 5529416 5529416 single base substitution G T downstream_gene_variant UCEC-US 11 5529416 5529416 single base substitution G T missense_variant A458D 1373C>A UCEC-US 11 5529853 5529853 single base substitution G A downstream_gene_variant UCEC-US 11 5529853 5529853 single base substitution G A synonymous_variant G312G 936C>T UCEC-US 11 5530048 5530048 single base substitution A G downstream_gene_variant UCEC-US 11 5530048 5530048 single base substitution A G synonymous_variant I247I 741T>C UCEC-US 11 5530464 5530464 single base substitution T C missense_variant T109A 325A>G UCEC-US 11 5530475 5530475 single base substitution G A missense_variant A105V 314C>T UCEC-US 11 5530614 5530614 single base substitution C T missense_variant D59N 175G>A UCEC-US 11 5530616 5530616 single base substitution G T missense_variant P58H 173C>A UCEC-US 11 5530637 5530637 single base substitution G T missense_variant S51Y 152C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3202 COSM4738790 c.1711C>A p.P571T Substitution - Missense 11:5507848-5507848 - TCGA-RC-A7SF-01 COSM76933 c.652C>T p.R218W Substitution - Missense 11:5508907-5508907 - YUNIBO COSM5372693 c.1906C>T p.Q636* Substitution - Nonsense 11:5507653-5507653 - Pat_53_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - RK189_C01 COSM1628044 c.359C>T p.P120L Substitution - Missense 11:5509200-5509200 - C086 COSM5541290 c.640C>T p.P214S Substitution - Missense 11:5508919-5508919 - LUAD-NYU184 COSM370718 c.1382C>G p.S461C Substitution - Missense 11:5508177-5508177 - T2931 COSM4738795 c.193T>A p.F65I Substitution - Missense 11:5509366-5509366 - TCGA-FS-A1ZQ-06 COSM3448818 c.1618C>T p.R540C Substitution - Missense 11:5507941-5507941 - TCGA-19-5950 COSM2156542 c.822C>T p.G274G Substitution - coding silent 11:5508737-5508737 - PT48 COSM5932924 c.1484C>T p.P495L Substitution - Missense 11:5508075-5508075 - TCGA-AX-A0J0-01 COSM928015 c.173C>A p.P58H Substitution - Missense 11:5509386-5509386 - TCGA-GN-A269-01 COSM1354397 c.174C>T p.P58P Substitution - coding silent 11:5509385-5509385 - Au8 COSM5607186 c.761T>C p.L254P Substitution - Missense 11:5508798-5508798 - 522_T COSM3953251 c.1794G>T p.M598I Substitution - Missense 11:5507765-5507765 - CSCC-49-T COSM928009 c.1395G>A p.T465T Substitution - coding silent 11:5508164-5508164 - 61 COSM5739150 c.1840G>A p.A614T Substitution - Missense 11:5507719-5507719 - PT49 COSM5935817 c.1409G>A p.G470E Substitution - Missense 11:5508150-5508150 - S00472 COSM316335 c.885G>C p.R295S Substitution - Missense 11:5508674-5508674 - ESCC_46 COSM5630472 c.982G>T p.D328Y Substitution - Missense 11:5508577-5508577 - TCGA-AP-A059-01 COSM928011 c.936C>T p.G312G Substitution - coding silent 11:5508623-5508623 - HCC26T COSM3666382 c.1676T>C p.I559T Substitution - Missense 11:5507883-5507883 - TCGA-D3-A3C6-06 COSM3448821 c.1389C>T p.S463S Substitution - coding silent 11:5508170-5508170 - S37_pre COSM5575058 c.1194G>C p.E398D Substitution - Missense 11:5508365-5508365 - CHC1741T COSM4805539 c.678C>T p.N226N Substitution - coding silent 11:5508881-5508881 - TCGA-EM-A2OY-01 COSM3368401 c.1792A>G p.M598V Substitution - Missense 11:5507767-5507767 - PCSI_0085_Pa_P COSM3375841 c.1524G>T p.L508L Substitution - coding silent 11:5508035-5508035 - PCSI_0085_Pa_P_526 COSM3375841 c.1524G>T p.L508L Substitution - coding silent 11:5508035-5508035 - 8031606 COSM3769337 c.1573C>T p.R525W Substitution - Missense 11:5507986-5507986 - YUKAT COSM5372697 c.1234T>G p.F412V Substitution - Missense 11:5508325-5508325 - PT49 COSM5935816 c.1114G>A p.E372K Substitution - Missense 11:5508445-5508445 - SC_9046 COSM4033597 c.1922C>T p.T641M Substitution - Missense 11:5507637-5507637 - TCGA-CH-5763-01 COSM1470456 c.1398A>G p.A466A Substitution - coding silent 11:5508161-5508161 - DLBCL-PatientM COSM221531 c.778G>T p.D260Y Substitution - Missense 11:5508781-5508781 - ATL347 COSM5704037 c.1564C>T p.Q522* Substitution - Nonsense 11:5507995-5507995 - 8057643 COSM4407449 c.159C>A p.R53R Substitution - coding silent 11:5509400-5509400 - TCGA-CA-6717-01 COSM1354382 c.1838A>G p.E613G Substitution - Missense 11:5507721-5507721 - TCGA-D7-6522-01 COSM4033597 c.1922C>T p.T641M Substitution - Missense 11:5507637-5507637 - I2L-P19Tb-Tumor-Organoid COSM4619392 c.475C>T p.R159W Substitution - Missense 11:5509084-5509084 - 49M COSM5593821 c.1157C>T p.S386L Substitution - Missense 11:5508402-5508402 - TCGA-AD-6889-01 COSM1354381 c.1864C>A p.Q622K Substitution - Missense 11:5507695-5507695 - 40M COSM3448845 c.344G>A p.G115E Substitution - Missense 11:5509215-5509215 - TCGA-EE-A2GO-06 COSM3448843 c.468C>T p.S156S Substitution - coding silent 11:5509091-5509091 - TCGA-B0-5710-01 COSM466914 c.1932C>T p.D644D Substitution - coding silent 11:5507627-5507627 - 587226 COSM1231597 c.193T>G p.F65V Substitution - Missense 11:5509366-5509366 - C0008T COSM3869366 c.1293G>A p.G431G Substitution - coding silent 11:5508266-5508266 - 2293773 COSM4607281 c.661C>G p.L221V Substitution - Missense 11:5508898-5508898 - RKO COSM1354396 c.389delC p.P130fs*5 Deletion - Frameshift 11:5509170-5509170 - TCGA-ER-A198-06 COSM3448837 c.960G>A p.Q320Q Substitution - coding silent 11:5508599-5508599 - TCGA-60-2698-01 COSM688979 c.696G>T p.E232D Substitution - Missense 11:5508863-5508863 - 19 COSM5747214 c.1250C>T p.T417I Substitution - Missense 11:5508309-5508309 - TCGA-AZ-4315-01 COSM1354383 c.1475A>G p.N492S Substitution - Missense 11:5508084-5508084 - HT115 COSM928016 c.152C>A p.S51Y Substitution - Missense 11:5509407-5509407 - TCGA-JW-A5VL-01 COSM4847162 c.898G>C p.D300H Substitution - Missense 11:5508661-5508661 - TCGA-66-2759-01 COSM688983 c.1531C>T p.L511F Substitution - Missense 11:5508028-5508028 - CSCC-44-T COSM4194299 c.1069G>A p.G357R Substitution - Missense 11:5508490-5508490 - TCGA-BR-8677-01 COSM4033607 c.667T>C p.F223L Substitution - Missense 11:5508892-5508892 - RK019_C01 COSM1628043 c.1807G>C p.V603L Substitution - Missense 11:5507752-5507752 - MO_1012 COSM5549377 c.842C>T p.A281V Substitution - Missense 11:5508717-5508717 - 260211 COSM3725905 c.757G>T p.V253L Substitution - Missense 11:5508802-5508802 - CSCC-5-T COSM3448825 c.1327G>A p.D443N Substitution - Missense 11:5508232-5508232 - YUDEXA COSM1475513 c.322C>T p.P108S Substitution - Missense 11:5509237-5509237 - 587338 COSM1231599 c.1285G>T p.G429C Substitution - Missense 11:5508274-5508274 - RK019_C COSM1628043 c.1807G>C p.V603L Substitution - Missense 11:5507752-5507752 - SJDES011-R COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - S01563 COSM316336 c.594G>T p.Q198H Substitution - Missense 11:5508965-5508965 - TCGA-EE-A29E-06 COSM3448841 c.733G>A p.E245K Substitution - Missense 11:5508826-5508826 - TCGA-FW-A3R5-06 COSM3869366 c.1293G>A p.G431G Substitution - coding silent 11:5508266-5508266 - sysucc-1150T COSM5452408 c.1574G>A p.R525Q Substitution - Missense 11:5507985-5507985 - S01563 COSM316336 c.594G>T p.Q198H Substitution - Missense 11:5508965-5508965 - CSCC-62-T COSM3448822 c.1361G>A p.R454K Substitution - Missense 11:5508198-5508198 - CSCC-37-T COSM4472327 c.1775C>T p.S592F Substitution - Missense 11:5507784-5507784 - TCGA-EE-A2MR-06 COSM3448825 c.1327G>A p.D443N Substitution - Missense 11:5508232-5508232 - TCGA-19-4068-01 COSM2156459 c.1429C>T p.L477L Substitution - coding silent 11:5508130-5508130 - 40M COSM3869366 c.1293G>A p.G431G Substitution - coding silent 11:5508266-5508266 - S00472 COSM316335 c.885G>C p.R295S Substitution - Missense 11:5508674-5508674 - TCGA-EB-A41B-01 COSM3448831 c.1136G>A p.R379K Substitution - Missense 11:5508423-5508423 - T3118 COSM3769337 c.1573C>T p.R525W Substitution - Missense 11:5507986-5507986 - TCGA-DA-A1I0-06 COSM1703466 c.97G>A p.E33K Substitution - Missense 11:5509462-5509462 - SNU-C4 COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - C086 COSM3869366 c.1293G>A p.G431G Substitution - coding silent 11:5508266-5508266 - HCC118T COSM5813839 c.1458G>C p.L486L Substitution - coding silent 11:5508101-5508101 - ccRCC-8 COSM1664861 c.450C>A p.F150L Substitution - Missense 11:5509109-5509109 - TCGA-24-2267-01 COSM73184 c.1316C>T p.T439I Substitution - Missense 11:5508243-5508243 - CSCC-10-T COSM4468800 c.1564C>A p.Q522K Substitution - Missense 11:5507995-5507995 - TCGA-18-3409-01 COSM688980 c.716G>T p.R239L Substitution - Missense 11:5508843-5508843 - CSCC-7-T COSM4525679 c.1346G>A p.G449E Substitution - Missense 11:5508213-5508213 - 587346 COSM1231598 c.1870C>T p.R624W Substitution - Missense 11:5507689-5507689 - LUAD-B00416 COSM330814 c.1872G>T p.R624R Substitution - coding silent 11:5507687-5507687 - YUWIA COSM5372692 c.1924G>A p.G642R Substitution - Missense 11:5507635-5507635 - TCGA-19-4068 COSM2156459 c.1429C>T p.L477L Substitution - coding silent 11:5508130-5508130 - SW48 COSM4194292 c.1306G>A p.G436R Substitution - Missense 11:5508253-5508253 - 5_PRE-TREATMENT COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - U343 COSM179210 c.175G>A p.D59N Substitution - Missense 11:5509384-5509384 - Pat_15_B COSM5838752 c.533C>T p.P178L Substitution - Missense 11:5509026-5509026 - TCGA-37-4135-01 COSM688984 c.1638G>A p.M546I Substitution - Missense 11:5507921-5507921 - LP6005334-DNA_E01 COSM543515 c.158G>A p.R53H Substitution - Missense 11:5509401-5509401 - TCGA-EB-A41A-01 COSM3448845 c.344G>A p.G115E Substitution - Missense 11:5509215-5509215 - BCM739T COSM4955644 c.1176A>G p.S392S Substitution - coding silent 11:5508383-5508383 - TCGA-AX-A05Z-01 COSM928016 c.152C>A p.S51Y Substitution - Missense 11:5509407-5509407 - YUKSI COSM3448836 c.966G>A p.G322G Substitution - coding silent 11:5508593-5508593 - TCGA-AX-A0J0-01 COSM928005 c.1968G>T p.*656Y Nonstop extension 11:5507591-5507591 - CHC1741T COSM4805539 c.678C>T p.N226N Substitution - coding silent 11:5508881-5508881 - pfg059T COSM3769337 c.1573C>T p.R525W Substitution - Missense 11:5507986-5507986 - T3021 COSM4738794 c.282G>A p.Q94Q Substitution - coding silent 11:5509277-5509277 - CSCC-29-T COSM4456235 c.1001C>T p.P334L Substitution - Missense 11:5508558-5508558 - TCGA-24-2281-01 COSM116766 c.1960C>G p.Q654E Substitution - Missense 11:5507599-5507599 - YUMAN COSM1686148 c.1141C>T p.P381S Substitution - Missense 11:5508418-5508418 - TCGA-AR-A24N-01 COSM1475513 c.322C>T p.P108S Substitution - Missense 11:5509237-5509237 - YULLON COSM1703465 c.532_533CC>TT p.P178L Substitution - Missense 11:5509026-5509027 - ATL014 COSM5575183 c.1165G>T p.E389* Substitution - Nonsense 11:5508394-5508394 - TCGA-EE-A29S-06 COSM3448828 c.1191C>T p.P397P Substitution - coding silent 11:5508368-5508368 - C089 COSM5543574 c.347C>T p.S116L Substitution - Missense 11:5509212-5509212 - Pat_16_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - 11M COSM5372696 c.1236C>T p.F412F Substitution - coding silent 11:5508323-5508323 - TCGA-D3-A2J8-06 COSM3448830 c.1151C>T p.S384L Substitution - Missense 11:5508408-5508408 - YUCLAT COSM1703466 c.97G>A p.E33K Substitution - Missense 11:5509462-5509462 - TCGA-06-0124 COSM2149287 c.1511_1512delAG p.Q504fs*24 Deletion - Frameshift 11:5508047-5508048 - ESCC-178T COSM3935498 c.1708G>A p.D570N Substitution - Missense 11:5507851-5507851 - TCGA-FW-A5DX-01 COSM3448823 c.1350T>G p.D450E Substitution - Missense 11:5508209-5508209 - YUBER COSM1686148 c.1141C>T p.P381S Substitution - Missense 11:5508418-5508418 - CPCG0372-F1 COSM4966590 c.1718C>A p.P573Q Substitution - Missense 11:5507841-5507841 - TCGA-D1-A17Q-01 COSM179210 c.175G>A p.D59N Substitution - Missense 11:5509384-5509384 - SM-4AX84 COSM4412801 c.790C>G p.P264A Substitution - Missense 11:5508769-5508769 - TCGA-FS-A1Z3-06 COSM3448829 c.1189C>T p.P397S Substitution - Missense 11:5508370-5508370 - TCGA-34-5231-01 COSM688978 c.444T>C p.R148R Substitution - coding silent 11:5509115-5509115 - TCGA-ET-A25R-01 COSM3368402 c.440A>G p.Y147C Substitution - Missense 11:5509119-5509119 - CSCC-29-T COSM4472470 c.1786C>T p.L596F Substitution - Missense 11:5507773-5507773 - A6 COSM5349697 c.574C>A p.L192I Substitution - Missense 11:5508985-5508985 - TCGA-BG-A0M8-01 COSM928018 c.48C>A p.V16V Substitution - coding silent 11:5509511-5509511 - TCGA-ER-A2NH-06 COSM3448835 c.1038C>T p.L346L Substitution - coding silent 11:5508521-5508521 - TCGA-AD-5900-01 COSM1354384 c.1457T>C p.L486P Substitution - Missense 11:5508102-5508102 - CSCC-55-T COSM4465529 c.1388C>T p.S463F Substitution - Missense 11:5508171-5508171 - 40M COSM5586949 c.1056C>T p.N352N Substitution - coding silent 11:5508503-5508503 - TCGA-AD-6895-01 COSM1354389 c.828T>C p.N276N Substitution - coding silent 11:5508731-5508731 - TCGA-ER-A193-06 COSM3448824 c.1338G>A p.S446S Substitution - coding silent 11:5508221-5508221 - TCGA-GN-A266-06 COSM3448819 c.1609G>A p.E537K Substitution - Missense 11:5507950-5507950 - 7285 COSM5613383 c.1789C>T p.H597Y Substitution - Missense 11:5507770-5507770 - Pat_40_A COSM5838753 c.287G>A p.R96H Substitution - Missense 11:5509272-5509272 - UM-SCC-17B COSM4599119 c.1803T>G p.D601E Substitution - Missense 11:5507756-5507756 - TCGA-BR-6452-01 COSM4033608 c.635A>G p.N212S Substitution - Missense 11:5508924-5508924 - TCGA-BR-8382-01 COSM4033602 c.1387T>C p.S463P Substitution - Missense 11:5508172-5508172 - TCGA-D1-A103-01 COSM928006 c.1609G>T p.E537* Substitution - Nonsense 11:5507950-5507950 - C086 COSM5541289 c.1375C>T p.P459S Substitution - Missense 11:5508184-5508184 - T155 COSM1176500 c.1744G>A p.A582T Substitution - Missense 11:5507815-5507815 - TCGA-B5-A0JY-01 COSM928007 c.1485A>G p.P495P Substitution - coding silent 11:5508074-5508074 - TCGA-BR-A4QM-01 COSM4033599 c.1844A>C p.H615P Substitution - Missense 11:5507715-5507715 - TCGA-GN-A269-01 COSM3448846 c.337A>G p.S113G Substitution - Missense 11:5509222-5509222 - TCGA-BR-8680-01 COSM4033604 c.1003A>C p.N335H Substitution - Missense 11:5508556-5508556 - BD134T COSM5494454 c.562C>T p.R188C Substitution - Missense 11:5508997-5508997 - YUMOKI COSM5372694 c.1552C>T p.P518S Substitution - Missense 11:5508007-5508007 - S02382 COSM5697731 c.718G>T p.V240L Substitution - Missense 11:5508841-5508841 - HCC60 COSM1604683 c.389C>T p.P130L Substitution - Missense 11:5509170-5509170 - CADO-ES1 COSM4194274 c.1700T>C p.M567T Substitution - Missense 11:5507859-5507859 - LP6005334-DNA_G01 COSM5034913 c.11G>T p.G4V Substitution - Missense 11:5509548-5509548 - TCGA-JX-A3Q0-01 COSM4824289 c.1110C>T p.S370S Substitution - coding silent 11:5508449-5508449 - TCGA-CG-5728-01 COSM4033598 c.1892G>A p.R631H Substitution - Missense 11:5507667-5507667 - CHC313T COSM4949923 c.889G>C p.E297Q Substitution - Missense 11:5508670-5508670 - YUQUEST COSM5372696 c.1236C>T p.F412F Substitution - coding silent 11:5508323-5508323 - 587228 COSM1180757 c.1774delT p.S592fs*11 Deletion - Frameshift 11:5507785-5507785 - TCGA-EE-A2GO-06 COSM3448822 c.1361G>A p.R454K Substitution - Missense 11:5508198-5508198 - TCGA-AP-A051-01 COSM928010 c.1373C>A p.A458D Substitution - Missense 11:5508186-5508186 - T3149 COSM4738789 c.1730C>A p.P577H Substitution - Missense 11:5507829-5507829 - YUOMEGA COSM5372698 c.643G>A p.E215K Substitution - Missense 11:5508916-5508916 - HCC60T COSM1604683 c.389C>T p.P130L Substitution - Missense 11:5509170-5509170 - TCGA-D3-A2JH-06 COSM179210 c.175G>A p.D59N Substitution - Missense 11:5509384-5509384 - HCC56T COSM1604682 c.619A>T p.I207F Substitution - Missense 11:5508940-5508940 - BD148T COSM5521213 c.1626A>T p.L542L Substitution - coding silent 11:5507933-5507933 - TCGA-DA-A1HY-06 COSM3448832 c.1109G>A p.S370N Substitution - Missense 11:5508450-5508450 - YUOMEGA COSM5372695 c.1325C>T p.P442L Substitution - Missense 11:5508234-5508234 - TCGA-AP-A059-01 COSM928013 c.325A>G p.T109A Substitution - Missense 11:5509234-5509234 - BD179T COSM5499876 c.1504C>A p.Q502K Substitution - Missense 11:5508055-5508055 - T3535 COSM4738792 c.1559C>T p.A520V Substitution - Missense 11:5508000-5508000 - Pat_44_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - LUAD-E00897 COSM364287 c.1339G>T p.G447W Substitution - Missense 11:5508220-5508220 - TCGA-18-4083-01 COSM688981 c.773A>G p.Y258C Substitution - Missense 11:5508786-5508786 - 2492714 COSM5607186 c.761T>C p.L254P Substitution - Missense 11:5508798-5508798 - 2492712 COSM5607186 c.761T>C p.L254P Substitution - Missense 11:5508798-5508798 - 49M COSM5593822 c.1782C>T p.P594P Substitution - coding silent 11:5507777-5507777 - TCGA-AZ-6598-01 COSM1354396 c.389delC p.P130fs*5 Deletion - Frameshift 11:5509170-5509170 - HCC2998 COSM4194300 c.1026C>A p.L342L Substitution - coding silent 11:5508533-5508533 - TCGA-EE-A3AA-06 COSM3448840 c.778G>A p.D260N Substitution - Missense 11:5508781-5508781 - HCC56 COSM1604682 c.619A>T p.I207F Substitution - Missense 11:5508940-5508940 - TCGA-D3-A3BZ-06 COSM3869365 c.1461G>C p.R487S Substitution - Missense 11:5508098-5508098 - TCGA-CG-4437-01 COSM4033601 c.1569C>G p.A523A Substitution - coding silent 11:5507990-5507990 - CHC892T COSM4794802 c.1827G>A p.Q609Q Substitution - coding silent 11:5507732-5507732 - TCGA-D9-A6EC-06 COSM4405247 c.1879G>A p.G627S Substitution - Missense 11:5507680-5507680 - TCGA-BF-A1Q0-01 COSM3448838 c.953G>A p.G318E Substitution - Missense 11:5508606-5508606 - sysucc-311T COSM5477640 c.998T>C p.F333S Substitution - Missense 11:5508561-5508561 - TCGA-AX-A05Z-01 COSM928008 c.1440G>A p.P480P Substitution - coding silent 11:5508119-5508119 - 2492711 COSM5607186 c.761T>C p.L254P Substitution - Missense 11:5508798-5508798 - TCGA-EE-A29D-06 COSM3448834 c.1065C>T p.S355S Substitution - coding silent 11:5508494-5508494 - B66 COSM1746307 c.210C>G p.L70L Substitution - coding silent 11:5509349-5509349 - TCGA-EW-A1IW-01 COSM1475512 c.867C>T p.T289T Substitution - coding silent 11:5508692-5508692 - BCM739T COSM4955644 c.1176A>G p.S392S Substitution - coding silent 11:5508383-5508383 - TCGA-F4-6463-01 COSM3687371 c.138G>T p.L46L Substitution - coding silent 11:5509421-5509421 - TCGA-EE-A2MK-06 COSM3448817 c.1639C>T p.P547S Substitution - Missense 11:5507920-5507920 - ESCC_37 COSM5628878 c.967G>C p.D323H Substitution - Missense 11:5508592-5508592 - TCGA-AG-A002-01 COSM264524 c.1801G>T p.D601Y Substitution - Missense 11:5507758-5507758 - TCGA-BG-A0M8-01 COSM928017 c.49C>A p.Q17K Substitution - Missense 11:5509510-5509510 - ESO-049 COSM1269649 c.400T>C p.L134L Substitution - coding silent 11:5509159-5509159 - ATL045 COSM5704038 c.497A>C p.E166A Substitution - Missense 11:5509062-5509062 - TCGA-32-5222-01 COSM3397773 c.1771C>T p.L591F Substitution - Missense 11:5507788-5507788 - TCGA-ER-A193-06 COSM3448836 c.966G>A p.G322G Substitution - coding silent 11:5508593-5508593 - S02328 COSM5691780 c.309A>T p.P103P Substitution - coding silent 11:5509250-5509250 - Pat_37_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - C086 COSM5541288 c.1723C>T p.P575S Substitution - Missense 11:5507836-5507836 - TCGA-A5-A0G9-01 COSM248181 c.823G>A p.G275S Substitution - Missense 11:5508736-5508736 - TCGA-B0-5098-01 COSM1492589 c.1272T>C p.G424G Substitution - coding silent 11:5508287-5508287 - TCGA-36-1571-01 COSM78744 c.1891C>G p.R631G Substitution - Missense 11:5507668-5507668 - TCGA-HU-8604-01 COSM3448846 c.337A>G p.S113G Substitution - Missense 11:5509222-5509222 - CSCC-11-T COSM4489020 c.341C>T p.P114L Substitution - Missense 11:5509218-5509218 - LUAD-B01145 COSM333223 c.1327G>T p.D443Y Substitution - Missense 11:5508232-5508232 - PR-00-1165 COSM248181 c.823G>A p.G275S Substitution - Missense 11:5508736-5508736 - TCGA-CD-A4MG-01 COSM4033600 c.1656G>A p.T552T Substitution - coding silent 11:5507903-5507903 - TCGA-DD-A39Z-01 COSM4916040 c.1840G>C p.A614P Substitution - Missense 11:5507719-5507719 - B66-Tumor COSM1746307 c.210C>G p.L70L Substitution - coding silent 11:5509349-5509349 - CHC892T COSM4794802 c.1827G>A p.Q609Q Substitution - coding silent 11:5507732-5507732 - BD217T COSM3448842 c.641C>T p.P214L Substitution - Missense 11:5508918-5508918 - TCGA-AM-5820-01 COSM429159 c.1871G>A p.R624Q Substitution - Missense 11:5507688-5507688 - TCGA-AM-5820-01 COSM3687369 c.802G>A p.A268T Substitution - Missense 11:5508757-5508757 - 587344 COSM1231598 c.1870C>T p.R624W Substitution - Missense 11:5507689-5507689 - Pat_15_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - C086 COSM5541291 c.600G>A p.L200L Substitution - coding silent 11:5508959-5508959 - ATL370 COSM4194287 c.1439C>T p.P480L Substitution - Missense 11:5508120-5508120 - C037 COSM4194269 c.1849C>T p.Q617* Substitution - Nonsense 11:5507710-5507710 - 587376 COSM1231600 c.5C>T p.A2V Substitution - Missense 11:5509554-5509554 - pfg060T COSM4033597 c.1922C>T p.T641M Substitution - Missense 11:5507637-5507637 - TCGA-EE-A2MR-06 COSM3448833 c.1070G>A p.G357E Substitution - Missense 11:5508489-5508489 - TCGA-CG-5728-01 COSM4033605 c.939A>G p.S313S Substitution - coding silent 11:5508620-5508620 - BD8T COSM543515 c.158G>A p.R53H Substitution - Missense 11:5509401-5509401 - TCGA-EE-A2MR-06 COSM3448842 c.641C>T p.P214L Substitution - Missense 11:5508918-5508918 - C70 COSM4619392 c.475C>T p.R159W Substitution - Missense 11:5509084-5509084 - TCGA-CM-6171-01 COSM1354397 c.174C>T p.P58P Substitution - coding silent 11:5509385-5509385 - HT115 COSM4194317 c.417C>A p.G139G Substitution - coding silent 11:5509142-5509142 - PS-155-3D COSM4423716 c.707G>T p.S236I Substitution - Missense 11:5508852-5508852 - PTC-7C COSM429159 c.1871G>A p.R624Q Substitution - Missense 11:5507688-5507688 - TCGA-DU-8161-01 COSM3967579 c.157C>T p.R53C Substitution - Missense 11:5509402-5509402 - HCC2998 COSM4194282 c.1517C>T p.P506L Substitution - Missense 11:5508042-5508042 - ME044T COSM229189 c.947G>A p.R316K Substitution - Missense 11:5508612-5508612 - STC246 COSM1354397 c.174C>T p.P58P Substitution - coding silent 11:5509385-5509385 - TCGA-FS-A4F5-06 COSM3448847 c.326C>T p.T109I Substitution - Missense 11:5509233-5509233 - TCGA-FW-A3R5-06 COSM3869367 c.1057C>T p.P353S Substitution - Missense 11:5508502-5508502 - TCGA-AA-3510-01 COSM1354385 c.1405C>T p.P469S Substitution - Missense 11:5508154-5508154 - TCGA-06-0686-01 COSM3397774 c.922T>A p.S308T Substitution - Missense 11:5508637-5508637 - TCGA-BR-4280-01 COSM4033596 c.1953G>A p.K651K Substitution - coding silent 11:5507606-5507606 - 8066491 COSM3769338 c.1145C>A p.P382Q Substitution - Missense 11:5508414-5508414 - PD7069a COSM5788800 c.1276G>T p.D426Y Substitution - Missense 11:5508283-5508283 - ME020T COSM225665 c.1109G>T p.S370I Substitution - Missense 11:5508450-5508450 - TCGA-AA-A010-01 COSM286250 c.1348G>T p.D450Y Substitution - Missense 11:5508211-5508211 - CSCC-31-T COSM4477746 c.217C>T p.P73S Substitution - Missense 11:5509342-5509342 - TCGA-AZ-4615-01 COSM3687370 c.654G>A p.R218R Substitution - coding silent 11:5508905-5508905 - Pat_58_B COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - SNUH_G73_S1 COSM429159 c.1871G>A p.R624Q Substitution - Missense 11:5507688-5507688 - Pat_41_B COSM4194289 c.1396G>A p.A466T Substitution - Missense 11:5508163-5508163 - TCGA-BR-6802-01 COSM4033603 c.1179C>T p.G393G Substitution - coding silent 11:5508380-5508380 - LUAD_E00565 COSM388958 c.850G>T p.D284Y Substitution - Missense 11:5508709-5508709 - HCC26 COSM3666382 c.1676T>C p.I559T Substitution - Missense 11:5507883-5507883 - TCGA-DA-A1HV-06 COSM3448844 c.393C>T p.A131A Substitution - coding silent 11:5509166-5509166 - YUKLAB COSM1703463 c.935G>C p.G312A Substitution - Missense 11:5508624-5508624 - PCSI_0085_Pa_X COSM3375841 c.1524G>T p.L508L Substitution - coding silent 11:5508035-5508035 - CSCC-17-T COSM4562554 c.931G>A p.G311R Substitution - Missense 11:5508628-5508628 - CHC313T COSM4949923 c.889G>C p.E297Q Substitution - Missense 11:5508670-5508670 - 513 COSM3724067 c.383G>T p.G128V Substitution - Missense 11:5509176-5509176 - CLL151 COSM1289564 c.1118C>G p.P373R Substitution - Missense 11:5508441-5508441 - 2492713 COSM5607186 c.761T>C p.L254P Substitution - Missense 11:5508798-5508798 - STC297 COSM5050874 c.1050C>T p.H350H Substitution - coding silent 11:5508509-5508509 - TCGA-A6-6140-01 COSM429159 c.1871G>A p.R624Q Substitution - Missense 11:5507688-5507688 - RK028_C01 COSM3739107 c.1178G>T p.G393V Substitution - Missense 11:5508381-5508381 - TCGA-AP-A059-01 COSM928014 c.314C>T p.A105V Substitution - Missense 11:5509245-5509245 - TCGA-46-3769-01 COSM688982 c.1414C>A p.P472T Substitution - Missense 11:5508145-5508145 - TCGA-AP-A054-01 COSM928012 c.741T>C p.I247I Substitution - coding silent 11:5508818-5508818 - 19M COSM5579928 c.1085G>A p.G362E Substitution - Missense 11:5508474-5508474 - BD130T COSM5516028 c.59A>T p.H20L Substitution - Missense 11:5509500-5509500 - CSCC-4-T COSM4518941 c.884_885GG>AA p.R295K Substitution - Missense 11:5508674-5508675 - 0012_CRUK_PC_0012_T1_DNA COSM4194266 c.1929C>T p.G643G Substitution - coding silent 11:5507630-5507630 - ATLL_A-01 COSM5575183 c.1165G>T p.E389* Substitution - Nonsense 11:5508394-5508394 - TCGA-D3-A3ML-06 COSM3448839 c.952G>A p.G318R Substitution - Missense 11:5508607-5508607 - TCGA-ET-A39N-01 COSM3368403 c.236G>A p.C79Y Substitution - Missense 11:5509323-5509323 - CSCC-54-T COSM4457954 c.1066C>T p.L356L Substitution - coding silent 11:5508493-5508493 - T263 COSM4738793 c.627T>C p.H209H Substitution - coding silent 11:5508932-5508932 - ME100L COSM231236 c.1690G>A p.D564N Substitution - Missense 11:5507869-5507869 - TCGA-EE-A29E-06 COSM3448827 c.1229C>T p.P410L Substitution - Missense 11:5508330-5508330 - YUBAN COSM1703464 c.694G>A p.E232K Substitution - Missense 11:5508865-5508865 - TCGA-12-0618 COSM2149287 c.1511_1512delAG p.Q504fs*24 Deletion - Frameshift 11:5508047-5508048 - TCGA-B7-5818-01 COSM4033606 c.827A>C p.N276T Substitution - Missense 11:5508732-5508732 - TCGA-AP-A0LM-01 COSM928009 c.1395G>A p.T465T Substitution - coding silent 11:5508164-5508164 - TCGA-EE-A3AE-06 COSM3448820 c.1413C>T p.I471I Substitution - coding silent 11:5508146-5508146 - 5_RESISTANT COSM1724855 c.869_871delCCA p.T290delT Deletion - In frame 11:5508688-5508690 - STC248 COSM5050875 c.992A>G p.N331S Substitution - Missense 11:5508567-5508567 - TCGA-AM-5820-01 COSM3752450 c.1650A>G p.A550A Substitution - coding silent 11:5507909-5507909 - TCGA-AQ-A0Y5-01 COSM1475511 c.1207A>C p.I403L Substitution - Missense 11:5508352-5508352 - PD4601a COSM165379 c.1456C>T p.L486L Substitution - coding silent 11:5508103-5508103 - 585210 COSM324159 c.1218G>T p.R406S Substitution - Missense 11:5508341-5508341 - S37_post COSM5575058 c.1194G>C p.E398D Substitution - Missense 11:5508365-5508365 - SKCO-1 COSM4194266 c.1929C>T p.G643G Substitution - coding silent 11:5507630-5507630 - 3844_T COSM3953252 c.132G>T p.Q44H Substitution - Missense 11:5509427-5509427 - CHC1629T COSM4791909 c.744T>A p.P248P Substitution - coding silent 11:5508815-5508815 - TCGA-DD-A4NG-01 COSM4926038 c.1653G>T p.G551G Substitution - coding silent 11:5507906-5507906 - YUFLA COSM1703462 c.1142C>T p.P381L Substitution - Missense 11:5508417-5508417 - TCGA-DK-A3WW-01 COSM3791553 c.273C>T p.I91I Substitution - coding silent 11:5509286-5509286 - CHC1629T COSM4791909 c.744T>A p.P248P Substitution - coding silent 11:5508815-5508815 - T578 COSM4738791 c.1612G>T p.A538S Substitution - Missense 11:5507947-5507947 - SNUH_G73_S1 COSM3752450 c.1650A>G p.A550A Substitution - coding silent 11:5507909-5507909 - TCGA-13-0893-01 COSM76933 c.652C>T p.R218W Substitution - Missense 11:5508907-5508907 - LUAD-RT-S01840 COSM384729 c.1546G>A p.A516T Substitution - Missense 11:5508013-5508013 - TCGA-CA-6717-01 COSM1354388 c.1195G>A p.E399K Substitution - Missense 11:5508364-5508364 - TCGA-EE-A3J5-06 COSM3448826 c.1321T>C p.L441L Substitution - coding silent 11:5508238-5508238 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.189184 11p15 605473 2399235|CGAP|BC036743|A/G|non-coding||2256|Validated; 2154635|dbSNP|BC036743|A/G|coding|Thr28Thr|184|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A Frameshift p.G642Wfs*45 c.1923_1924insT 11 5528865 COREAD A G Missense p.F65L c.193T>C 11 5530596 STAD A T Missense p.S308T c.922T>A 11 5529867 GBM A T Missense p.S36T c.106T>A 11 5530683 LUAD C A Missense p.G322W c.964G>T 11 5529825 LUAD C A Missense p.Q198H c.594G>T 11 5530195 SCLC C A Missense p.R406S c.1218G>T 11 5529571 SCLC C A Missense p.R454M c.1361G>T 11 5529428 LUAD C A Missense p.S370I c.1109G>T 11 5529680 CM C A Nonsense p.E528* c.1582G>T 11 5529207 CM C G Missense p.R295S c.885G>C 11 5529904 SCLC C G Missense p.R487S c.1461G>C 11 5529328 CM C G Missense p.V603L c.1807G>C 11 5528982 HC C T Missense p.A268T c.802G>A 11 5529987 HNSC C T Missense p.C79Y c.236G>A 11 5530553 THCA C T Missense p.D260N c.778G>A 11 5530011 CM C T Missense p.D34N c.100G>A 11 5530689 CM C T Missense p.D564N c.1690G>A 11 5529099 CM C T Missense p.D59N c.175G>A 11 5530614 CM C T Missense p.E33K c.97G>A 11 5530692 CM C T Missense p.E621K c.1861G>A 11 5528928 CM C T Missense p.G318E c.953G>A 11 5529836 CM C T Missense p.G318R c.952G>A 11 5529837 CM C T Missense p.M296I c.888G>A 11 5529901 CM C T Missense p.M546I c.1638G>A 11 5529151 LUSC C T Missense p.R316K c.947G>A 11 5529842 CM C T Missense p.R454K c.1361G>A 11 5529428 CM C T Missense p.R53H c.158G>A 11 5530631 LUAD C T Missense p.R631H c.1892G>A 11 5528897 STAD C T Missense p.S370N c.1109G>A 11 5529680 CM G A Missense p.H597Y c.1789C>T 11 5529000 CM G A Missense p.H597Y c.1789C>T 11 5529000 NSCLC G A Missense p.L511F c.1531C>T 11 5529258 LUSC G A Missense p.L591F c.1771C>T 11 5529018 GBM G A Missense p.P108S c.322C>T 11 5530467 BRCA G A Missense p.P397S c.1189C>T 11 5529600 CM G A Missense p.P547S c.1639C>T 11 5529150 CM G A Missense p.P577S c.1729C>T 11 5529060 CM G A Missense p.R218W c.652C>T 11 5530137 OV G A Missense p.R53C c.157C>T 11 5530632 LGG G A Missense p.R540C c.1618C>T 11 5529171 CM G A Missense p.S156F c.467C>T 11 5530322 CM G A Missense p.S384L c.1151C>T 11 5529638 CM G A Missense p.S408F c.1223C>T 11 5529566 CM G A Missense p.S655L c.1964C>T 11 5528825 COREAD G A Missense p.T439I c.1316C>T 11 5529473 OV G C Missense p.L63V c.187C>G 11 5530602 ALL G C Missense p.N335K c.1005C>G 11 5529784 LUAD G C Missense p.P373R c.1118C>G 11 5529671 CLL G C Missense p.P442R c.1325C>G 11 5529464 LUAD G C Missense p.Q119E c.355C>G 11 5530434 HNSC G C Missense p.Q654E c.1960C>G 11 5528829 OV G C Missense p.R631G c.1891C>G 11 5528898 OV G - Frameshift p.P382Hfs*20 c.1145delC 11 5529644 LUSC GG TA Missense p.P29L c.86_87delinsTA 11 5530702 CM G T Missense p.L543I c.1627C>A 11 5529162 STAD G T Missense p.P118H c.353C>A 11 5530436 HNSC G T Missense p.P472T c.1414C>A 11 5529375 LUSC G T Missense p.P474H c.1421C>A 11 5529368 HNSC T A Missense p.K47M c.140A>T 11 5530649 LUAD T A Missense p.M197L c.589A>T 11 5530200 CM T C Missense p.M598V c.1792A>G 11 5528997 THCA T C Missense p.N335S c.1004A>G 11 5529785 CM T C Missense p.S113G c.337A>G 11 5530452 CM T C Missense p.Y147C c.440A>G 11 5530349 THCA T C Missense p.Y258C c.773A>G 11 5530016 LUSC TGG - InFrameDeletion p.T290delT c.869_871delCCA 11 5529918 CM TGG - InFrameDeletion p.T290delT c.869_871delCCA 11 5529918 GBM TGG - InFrameDeletion p.T290delT c.869_871delCCA 11 5529918 HNSC TGG - InFrameDeletion p.T290delT c.869_871delCCA 11 5529918 PRAD T G Missense p.I403L c.1207A>C 11 5529582 BRCA T G Missense p.N276T c.827A>C 11 5529962 STAD