Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 11 70255949 70255949 + Silent SNP G G C TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr11:70255949G>C c.174G>C c.(172-174)ctG>ctC p.L58L BLCA 11 70263227 70263227 + Missense_Mutation SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr11:70263227G>A c.566G>A c.(565-567)aGa>aAa p.R189K BLCA 11 70265929 70265929 + Missense_Mutation SNP C C G TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr11:70265929C>G c.646C>G c.(646-648)Caa>Gaa p.Q216E BLCA 11 70266505 70266505 + Splice_Site SNP G G C TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr11:70266505G>C c.e10-1 BLCA 11 70267647 70267647 + Missense_Mutation SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr11:70267647G>A c.862G>A c.(862-864)Gat>Aat p.D288N BLCA 11 70269092 70269092 + Silent SNP G G A TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr11:70269092G>A c.948G>A c.(946-948)cgG>cgA p.R316R BLCA 11 70277332 70277332 + Silent SNP G G C TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr11:70277332G>C c.1212G>C c.(1210-1212)gtG>gtC p.V404V BLCA 11 70279261 70279261 + Missense_Mutation SNP G G A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr11:70279261G>A c.1321G>A c.(1321-1323)Gag>Aag p.E441K BLCA 11 70279289 70279289 + Missense_Mutation SNP C C G TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr11:70279289C>G c.1349C>G c.(1348-1350)gCc>gGc p.A450G BLCA 11 70279317 70279317 + Silent SNP G G A TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chr11:70279317G>A c.1377G>A c.(1375-1377)caG>caA p.Q459Q BLCA 11 70281143 70281143 + Missense_Mutation SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr11:70281143G>A c.1528G>A c.(1528-1530)Gag>Aag p.E510K BLCA 11 70281161 70281161 + Missense_Mutation SNP G G A TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr11:70281161G>A c.1546G>A c.(1546-1548)Gat>Aat p.D516N BLCA 11 70281184 70281184 + Missense_Mutation SNP G G C TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr11:70281184G>C c.1569G>C c.(1567-1569)gaG>gaC p.E523D BLCA 11 70281229 70281229 + Silent SNP C C T TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr11:70281229C>T c.1614C>T c.(1612-1614)taC>taT p.Y538Y BRCA 11 70256029 70256029 + Missense_Mutation SNP G G C TCGA-A8-A07B-01A-11W-A019-09 TCGA-A8-A07B-10A-01W-A021-09 g.chr11:70256029G>C c.254G>C c.(253-255)gGa>gCa p.G85A BRCA 11 70279792 70279792 + Missense_Mutation SNP T T G TCGA-OL-A5DA-01A-11D-A27P-09 TCGA-OL-A5DA-10A-01D-A27P-09 g.chr11:70279792T>G c.1484T>G c.(1483-1485)aTc>aGc p.I495S CESC 11 70275181 70275181 + Missense_Mutation SNP G G C TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr11:70275181G>C c.1052G>C c.(1051-1053)aGa>aCa p.R351T COAD 11 70253451 70253451 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:70253451C>T c.48C>T c.(46-48)gaC>gaT p.D16D COAD 11 70260715 70260715 + Missense_Mutation SNP G G T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr11:70260715G>T c.359G>T c.(358-360)gGc>gTc p.G120V COAD 11 70260753 70260753 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:70260753G>T c.397G>T c.(397-399)Gat>Tat p.D133Y COAD 11 70263207 70263207 + Silent SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:70263207G>A c.546G>A c.(544-546)acG>acA p.T182T COAD 11 70269075 70269075 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr11:70269075G>A c.931G>A c.(931-933)Ggg>Agg p.G311R COAD 11 70269076 70269076 + Missense_Mutation SNP G G A TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:70269076G>A c.932G>A c.(931-933)gGg>gAg p.G311E COAD 11 70277323 70277323 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:70277323G>A c.1203G>A c.(1201-1203)acG>acA p.T401T COAD 11 70281196 70281196 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:70281196C>T c.1581C>T c.(1579-1581)gaC>gaT p.D527D COAD 11 70281208 70281208 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:70281208C>T c.1593C>T c.(1591-1593)cgC>cgT p.R531R COADREAD 11 70253451 70253451 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:70253451C>T c.48C>T c.(46-48)gaC>gaT p.D16D COADREAD 11 70260715 70260715 + Missense_Mutation SNP G G T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr11:70260715G>T c.359G>T c.(358-360)gGc>gTc p.G120V COADREAD 11 70260753 70260753 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:70260753G>T c.397G>T c.(397-399)Gat>Tat p.D133Y COADREAD 11 70263207 70263207 + Silent SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:70263207G>A c.546G>A c.(544-546)acG>acA p.T182T COADREAD 11 70265868 70265868 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:70265868C>T c.585C>T c.(583-585)ttC>ttT p.F195F COADREAD 11 70269075 70269075 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr11:70269075G>A c.931G>A c.(931-933)Ggg>Agg p.G311R COADREAD 11 70269076 70269076 + Missense_Mutation SNP G G A TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr11:70269076G>A c.932G>A c.(931-933)gGg>gAg p.G311E COADREAD 11 70277323 70277323 + Silent SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:70277323G>A c.1203G>A c.(1201-1203)acG>acA p.T401T COADREAD 11 70277323 70277323 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:70277323G>A c.1203G>A c.(1201-1203)acG>acA p.T401T COADREAD 11 70279774 70279774 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:70279774A>G c.1466A>G c.(1465-1467)tAc>tGc p.Y489C COADREAD 11 70281196 70281196 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:70281196C>T c.1581C>T c.(1579-1581)gaC>gaT p.D527D COADREAD 11 70281208 70281208 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:70281208C>T c.1593C>T c.(1591-1593)cgC>cgT p.R531R DLBC 11 70265880 70265880 + Silent SNP C C T TCGA-RQ-A68N-01A-11D-A31X-10 TCGA-RQ-A68N-10A-01D-A31X-10 g.chr11:70265880C>T c.597C>T c.(595-597)taC>taT p.Y199Y DLBC 11 70279759 70279759 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:70279759G>A c.1451G>A c.(1450-1452)aGc>aAc p.S484N ESCA 11 70277335 70277335 + Silent SNP G G A TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr11:70277335G>A c.1215G>A c.(1213-1215)tcG>tcA p.S405S ESCA 11 70281137 70281137 + Missense_Mutation SNP G G A TCGA-LN-A8I1-01A-11D-A36J-09 TCGA-LN-A8I1-10A-01D-A36M-09 g.chr11:70281137G>A c.1522G>A c.(1522-1524)Gat>Aat p.D508N GBM 11 70255986 70255986 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 g.chr11:70255986G>A c.211G>A c.(211-213)Gag>Aag p.E71K GBM 11 70266538 70266538 + Missense_Mutation SNP G G A TCGA-26-6174-01A-21D-1845-08 TCGA-26-6174-10A-01D-1845-08 g.chr11:70266538G>A c.712G>A c.(712-714)Gtg>Atg p.V238M GBM 11 70279266 70279266 + Silent SNP G G A TCGA-06-5410-01A-01D-1696-08 TCGA-06-5410-10A-01D-1696-08 g.chr11:70279266G>A c.1326G>A c.(1324-1326)ccG>ccA p.P442P GBMLGG 11 70255986 70255986 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 g.chr11:70255986G>A c.211G>A c.(211-213)Gag>Aag p.E71K GBMLGG 11 70261803 70261803 + Missense_Mutation SNP A A G TCGA-E1-5322-01A-01D-1468-08 TCGA-E1-5322-10A-01D-1468-08 g.chr11:70261803A>G c.437A>G c.(436-438)gAg>gGg p.E146G GBMLGG 11 70266538 70266538 + Missense_Mutation SNP G G A TCGA-26-6174-01A-21D-1845-08 TCGA-26-6174-10A-01D-1845-08 g.chr11:70266538G>A c.712G>A c.(712-714)Gtg>Atg p.V238M GBMLGG 11 70275272 70275272 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:70275272G>A c.1143G>A c.(1141-1143)cgG>cgA p.R381R GBMLGG 11 70279266 70279266 + Silent SNP G G A TCGA-06-5410-01A-01D-1696-08 TCGA-06-5410-10A-01D-1696-08 g.chr11:70279266G>A c.1326G>A c.(1324-1326)ccG>ccA p.P442P HNSC 11 70253636 70253636 + Missense_Mutation SNP G G A TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr11:70253636G>A c.100G>A c.(100-102)Gag>Aag p.E34K HNSC 11 70253658 70253658 + Missense_Mutation SNP C C G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:70253658C>G c.122C>G c.(121-123)gCc>gGc p.A41G HNSC 11 70260656 70260656 + Silent SNP C C T TCGA-BB-4225-01A-01D-1434-08 TCGA-BB-4225-10A-01D-1434-08 g.chr11:70260656C>T c.300C>T c.(298-300)gtC>gtT p.V100V HNSC 11 70263146 70263146 + Missense_Mutation SNP A A G TCGA-CV-6952-01A-11D-1912-08 TCGA-CV-6952-10A-01D-1912-08 g.chr11:70263146A>G c.485A>G c.(484-486)tAt>tGt p.Y162C HNSC 11 70263192 70263192 + Missense_Mutation SNP C C A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr11:70263192C>A c.531C>A c.(529-531)gaC>gaA p.D177E HNSC 11 70265886 70265886 + Silent SNP C C T TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chr11:70265886C>T c.603C>T c.(601-603)atC>atT p.I201I HNSC 11 70267604 70267604 + Silent SNP C C T TCGA-BA-6872-01A-11D-1870-08 TCGA-BA-6872-10A-01D-1870-08 g.chr11:70267604C>T c.819C>T c.(817-819)ttC>ttT p.F273F HNSC 11 70271437 70271437 + Splice_Site SNP G G A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr11:70271437G>A c.e13-1 HNSC 11 70275169 70275178 + Frame_Shift_Del DEL CAAGTAACAT CAAGTAACAT - TCGA-CN-6989-01A-11D-1912-08 TCGA-CN-6989-10A-01D-1912-08 g.chr11:70275169_70275178delCAAGTAACAT c.1040_1049delCAAGTAACAT c.(1039-1050)acaagtaacatcfs p.TSNI347fs HNSC 11 70281209 70281209 + Missense_Mutation SNP G G T TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr11:70281209G>T c.1594G>T c.(1594-1596)Ggg>Tgg p.G532W HNSC 11 70281210 70281210 + Missense_Mutation SNP G G T TCGA-CV-5444-01A-02D-1512-08 TCGA-CV-5444-11A-01D-1512-08 g.chr11:70281210G>T c.1595G>T c.(1594-1596)gGg>gTg p.G532V HNSC 11 70281216 70281216 + Missense_Mutation SNP G G C TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr11:70281216G>C c.1601G>C c.(1600-1602)tGc>tCc p.C534S HNSC 11 70281261 70281261 + Missense_Mutation SNP G G A TCGA-CV-5970-01A-11D-1683-08 TCGA-CV-5970-10A-01D-1870-08 g.chr11:70281261G>A c.1646G>A c.(1645-1647)cGg>cAg p.R549Q HNSC 11 70281676 70281676 + 3'UTR SNP G G A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr11:70281676G>A HNSC 11 70281737 70281737 + 3'UTR SNP G G C TCGA-BA-4078-01A-01D-1434-08 TCGA-BA-4078-10A-01D-1434-08 g.chr11:70281737G>C HNSC 11 70282397 70282397 + 3'UTR SNP C C T TCGA-C9-A47Z-01A-11D-A24D-08 TCGA-C9-A47Z-10A-01D-A24F-08 g.chr11:70282397C>T HNSC 11 70282397 70282397 + 3'UTR SNP C C T TCGA-CN-A498-01A-11D-A24D-08 TCGA-CN-A498-10A-01D-A24F-08 g.chr11:70282397C>T LGG 11 70261803 70261803 + Missense_Mutation SNP A A G TCGA-E1-5322-01A-01D-1468-08 TCGA-E1-5322-10A-01D-1468-08 g.chr11:70261803A>G c.437A>G c.(436-438)gAg>gGg p.E146G LGG 11 70275272 70275272 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:70275272G>A c.1143G>A c.(1141-1143)cgG>cgA p.R381R LIHC 11 70260723 70260723 + Missense_Mutation SNP G G A TCGA-FV-A23B-01A-11D-A16V-10 TCGA-FV-A23B-11A-11D-A16V-10 g.chr11:70260723G>A c.367G>A c.(367-369)Ggc>Agc p.G123S LIHC 11 70269063 70269063 + Missense_Mutation SNP G G A TCGA-DD-A4NK-01A-11D-A28X-10 TCGA-DD-A4NK-10A-01D-A28X-10 g.chr11:70269063G>A c.919G>A c.(919-921)Ggc>Agc p.G307S LIHC 11 70279767 70279767 + Missense_Mutation SNP G G T TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chr11:70279767G>T c.1459G>T c.(1459-1461)Gat>Tat p.D487Y LUAD 11 70253623 70253623 + Splice_Site SNP G G C TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr11:70253623G>C c.e4-1 LUAD 11 70263174 70263174 + Missense_Mutation SNP G G T TCGA-05-4420-01A-01D-1265-08 TCGA-05-4420-10A-01D-1265-08 g.chr11:70263174G>T c.513G>T c.(511-513)aaG>aaT p.K171N LUAD 11 70277324 70277324 + Frame_Shift_Del DEL C C - TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr11:70277324delC c.1204delC c.(1204-1206)cccfs p.P403fs LUAD 11 70279240 70279240 + Nonsense_Mutation SNP A A T TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr11:70279240A>T c.1300A>T c.(1300-1302)Aga>Tga p.R434* LUAD 11 70279260 70279260 + Silent SNP G G A TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr11:70279260G>A c.1320G>A c.(1318-1320)acG>acA p.T440T LUAD 11 70279299 70279299 + Silent SNP C C T TCGA-55-7728-01A-11D-2184-08 TCGA-55-7728-10A-01D-2184-08 g.chr11:70279299C>T c.1359C>T c.(1357-1359)taC>taT p.Y453Y LUAD 11 70279327 70279327 + Missense_Mutation SNP G G C TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr11:70279327G>C c.1387G>C c.(1387-1389)Gcc>Ccc p.A463P LUAD 11 70279782 70279782 + Missense_Mutation SNP G G T TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr11:70279782G>T c.1474G>T c.(1474-1476)Gat>Tat p.D492Y LUAD 11 70281797 70281797 + 3'UTR SNP C C T TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr11:70281797C>T LUAD 11 70282409 70282409 + 3'UTR SNP G G T TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr11:70282409G>T LUSC 11 70255985 70255985 + Missense_Mutation SNP G G T TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr11:70255985G>T c.210G>T c.(208-210)aaG>aaT p.K70N LUSC 11 70260667 70260667 + Missense_Mutation SNP A A G TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chr11:70260667A>G c.311A>G c.(310-312)tAt>tGt p.Y104C LUSC 11 70266527 70266527 + Missense_Mutation SNP G G A TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chr11:70266527G>A c.701G>A c.(700-702)gGa>gAa p.G234E LUSC 11 70277370 70277370 + Nonsense_Mutation SNP C C A TCGA-18-3412-01A-01D-0983-08 TCGA-18-3412-11A-01D-0983-08 g.chr11:70277370C>A c.1250C>A c.(1249-1251)tCg>tAg p.S417* LUSC 11 70281197 70281197 + Missense_Mutation SNP G G C TCGA-22-4604-01A-01D-1267-08 TCGA-22-4604-11A-01D-1267-08 g.chr11:70281197G>C c.1582G>C c.(1582-1584)Ggc>Cgc p.G528R OV 11 70269076 70269076 + Missense_Mutation SNP G G C TCGA-13-1512-01A-01W-0545-08 TCGA-13-1512-10A-01W-0546-08 g.chr11:70269076G>C c.932G>C c.(931-933)gGg>gCg p.G311A PAAD 11 70256068 70256068 + Splice_Site SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:70256068T>C c.e5+2 PAAD 11 70281225 70281225 + Missense_Mutation SNP G G A TCGA-3A-A9IC-01A-11D-A38G-08 TCGA-3A-A9IC-10A-01D-A38J-08 g.chr11:70281225G>A c.1610G>A c.(1609-1611)cGg>cAg p.R537Q PRAD 11 70265948 70265948 + Missense_Mutation SNP A A G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:70265948A>G c.665A>G c.(664-666)cAc>cGc p.H222R PRAD 11 70282413 70282413 + 3'UTR SNP C C T TCGA-J4-A6G3-01A-11D-A30X-08 TCGA-J4-A6G3-10A-01D-A30X-08 g.chr11:70282413C>T READ 11 70265868 70265868 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:70265868C>T c.585C>T c.(583-585)ttC>ttT p.F195F READ 11 70277323 70277323 + Silent SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr11:70277323G>A c.1203G>A c.(1201-1203)acG>acA p.T401T READ 11 70279774 70279774 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:70279774A>G c.1466A>G c.(1465-1467)tAc>tGc p.Y489C SARC 11 70255965 70255965 + Nonsense_Mutation SNP C C T TCGA-DX-A2J1-01A-11D-A21Q-09 TCGA-DX-A2J1-10A-01D-A21Q-09 g.chr11:70255965C>T c.190C>T c.(190-192)Caa>Taa p.Q64* SARC 11 70265954 70265954 + Frame_Shift_Del DEL C C - TCGA-MB-A8JK-01A-11D-A36J-09 TCGA-MB-A8JK-10A-01D-A36M-09 g.chr11:70265954delC c.671delC c.(670-672)tccfs p.S224fs SARC 11 70269070 70269070 + Missense_Mutation SNP A A G TCGA-K1-A3PN-01A-11D-A228-09 TCGA-K1-A3PN-10A-01D-A22A-09 g.chr11:70269070A>G c.926A>G c.(925-927)aAg>aGg p.K309R SARC 11 70281823 70281823 + 3'UTR SNP G G A TCGA-SG-A6Z4-01A-22D-A33E-09 TCGA-SG-A6Z4-10A-01D-A33H-09 g.chr11:70281823G>A SKCM 11 70260694 70260694 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:70260694C>T c.338C>T c.(337-339)tCg>tTg p.S113L SKCM 11 70260710 70260710 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:70260710C>T c.354C>T c.(352-354)gtC>gtT p.V118V SKCM 11 70263215 70263215 + Missense_Mutation SNP A A T TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr11:70263215A>T c.554A>T c.(553-555)cAc>cTc p.H185L SKCM 11 70265886 70265886 + Silent SNP C C T TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr11:70265886C>T c.603C>T c.(601-603)atC>atT p.I201I SKCM 11 70267599 70267599 + Missense_Mutation SNP A A G TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr11:70267599A>G c.814A>G c.(814-816)Aaa>Gaa p.K272E SKCM 11 70275245 70275245 + Silent SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr11:70275245G>A c.1116G>A c.(1114-1116)gaG>gaA p.E372E SKCM 11 70279378 70279378 + Missense_Mutation SNP C C T TCGA-GN-A4U8-06A-11D-A32N-08 TCGA-GN-A4U8-10B-01D-A32N-08 g.chr11:70279378C>T c.1438C>T c.(1438-1440)Ccc>Tcc p.P480S SKCM 11 70281742 70281742 + 3'UTR SNP G G C TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:70281742G>C

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 70266524 70266524 single base substitution G A 5_prime_UTR_variant BLCA-CN 11 70266524 70266524 single base substitution G A downstream_gene_variant BLCA-CN 11 70266524 70266524 single base substitution G A exon_variant BLCA-CN 11 70266524 70266524 single base substitution G A missense_variant G233E 698G>A BLCA-CN 11 70266524 70266524 single base substitution G A upstream_gene_variant BLCA-CN 11 70271437 70271437 single base substitution G A downstream_gene_variant BLCA-CN 11 70271437 70271437 single base substitution G A splice_acceptor_variant BLCA-CN 11 70271437 70271437 single base substitution G A upstream_gene_variant BLCA-CN 11 70279755 70279755 single base substitution G A downstream_gene_variant BLCA-CN 11 70279755 70279755 single base substitution G A exon_variant BLCA-CN 11 70279755 70279755 single base substitution G A missense_variant D140N 418G>A BLCA-CN 11 70279755 70279755 single base substitution G A missense_variant D167N 499G>A BLCA-CN 11 70279755 70279755 single base substitution G A missense_variant D446N 1336G>A BLCA-CN 11 70279755 70279755 single base substitution G A missense_variant D483N 1447G>A BLCA-CN 11 70279755 70279755 single base substitution G A splice_region_variant BLCA-US 11 70265929 70265929 single base substitution C G downstream_gene_variant BLCA-US 11 70265929 70265929 single base substitution C G exon_variant BLCA-US 11 70265929 70265929 single base substitution C G missense_variant Q197E 589C>G BLCA-US 11 70265929 70265929 single base substitution C G missense_variant Q216E 646C>G BLCA-US 11 70265929 70265929 single base substitution C G upstream_gene_variant BLCA-US 11 70277332 70277332 single base substitution G C 3_prime_UTR_variant BLCA-US 11 70277332 70277332 single base substitution G C downstream_gene_variant BLCA-US 11 70277332 70277332 single base substitution G C exon_variant BLCA-US 11 70277332 70277332 single base substitution G C synonymous_variant V367V 1101G>C BLCA-US 11 70277332 70277332 single base substitution G C synonymous_variant V404V 1212G>C BLCA-US 11 70277332 70277332 single base substitution G C synonymous_variant V61V 183G>C BLCA-US 11 70277332 70277332 single base substitution G C synonymous_variant V88V 264G>C BLCA-US 11 70281143 70281143 single base substitution G A 3_prime_UTR_variant BLCA-US 11 70281143 70281143 single base substitution G A missense_variant E167K 499G>A BLCA-US 11 70281143 70281143 single base substitution G A missense_variant E194K 580G>A BLCA-US 11 70281143 70281143 single base substitution G A missense_variant E473K 1417G>A BLCA-US 11 70281143 70281143 single base substitution G A missense_variant E510K 1528G>A BLCA-US 11 70281229 70281229 single base substitution C T 3_prime_UTR_variant BLCA-US 11 70281229 70281229 single base substitution C T splice_region_variant BLCA-US 11 70281229 70281229 single base substitution C T synonymous_variant Y501Y 1503C>T BLCA-US 11 70281229 70281229 single base substitution C T synonymous_variant Y538Y 1614C>T BRCA-EU 11 70239618 70239618 single base substitution G C upstream_gene_variant BRCA-EU 11 70239710 70239710 single base substitution C G upstream_gene_variant BRCA-EU 11 70242104 70242104 single base substitution G A upstream_gene_variant BRCA-EU 11 70242785 70242785 single base substitution A T upstream_gene_variant BRCA-EU 11 70242786 70242786 single base substitution T A upstream_gene_variant BRCA-EU 11 70243412 70243412 single base substitution C G upstream_gene_variant BRCA-EU 11 70243581 70243581 single base substitution C T upstream_gene_variant BRCA-EU 11 70245615 70245615 single base substitution C A intron_variant BRCA-EU 11 70245658 70245658 single base substitution T C intron_variant BRCA-EU 11 70245931 70245931 single base substitution G A intron_variant BRCA-EU 11 70249423 70249423 single base substitution T C intron_variant BRCA-EU 11 70249423 70249423 single base substitution T C upstream_gene_variant BRCA-EU 11 70249424 70249424 single base substitution A C intron_variant BRCA-EU 11 70249424 70249424 single base substitution A C upstream_gene_variant BRCA-EU 11 70249534 70249534 single base substitution C T intron_variant BRCA-EU 11 70249534 70249534 single base substitution C T upstream_gene_variant BRCA-EU 11 70250839 70250839 single base substitution T C intron_variant BRCA-EU 11 70250839 70250839 single base substitution T C upstream_gene_variant BRCA-EU 11 70252097 70252097 single base substitution C A intron_variant BRCA-EU 11 70252097 70252097 single base substitution C A upstream_gene_variant BRCA-EU 11 70252476 70252476 single base substitution A G intron_variant BRCA-EU 11 70252476 70252476 single base substitution A G upstream_gene_variant BRCA-EU 11 70253199 70253199 single base substitution C T intron_variant BRCA-EU 11 70253199 70253199 single base substitution C T upstream_gene_variant BRCA-EU 11 70253972 70253972 single base substitution C G exon_variant BRCA-EU 11 70253972 70253972 single base substitution C G intron_variant BRCA-EU 11 70254156 70254156 single base substitution G A exon_variant BRCA-EU 11 70254156 70254156 single base substitution G A intron_variant BRCA-EU 11 70256079 70256079 single base substitution C T downstream_gene_variant BRCA-EU 11 70256079 70256079 single base substitution C T intron_variant BRCA-EU 11 70256079 70256079 single base substitution C T upstream_gene_variant BRCA-EU 11 70256515 70256515 single base substitution G A downstream_gene_variant BRCA-EU 11 70256515 70256515 single base substitution G A exon_variant BRCA-EU 11 70256515 70256515 single base substitution G A intron_variant BRCA-EU 11 70256515 70256515 single base substitution G A upstream_gene_variant BRCA-EU 11 70256558 70256558 single base substitution C T downstream_gene_variant BRCA-EU 11 70256558 70256558 single base substitution C T intron_variant BRCA-EU 11 70256558 70256558 single base substitution C T upstream_gene_variant BRCA-EU 11 70257267 70257267 single base substitution G C downstream_gene_variant BRCA-EU 11 70257267 70257267 single base substitution G C intron_variant BRCA-EU 11 70257267 70257267 single base substitution G C upstream_gene_variant BRCA-EU 11 70258249 70258249 single base substitution C G downstream_gene_variant BRCA-EU 11 70258249 70258249 single base substitution C G intron_variant BRCA-EU 11 70258249 70258249 single base substitution C G upstream_gene_variant BRCA-EU 11 70259461 70259461 single base substitution C A downstream_gene_variant BRCA-EU 11 70259461 70259461 single base substitution C A intron_variant BRCA-EU 11 70259461 70259461 single base substitution C A upstream_gene_variant BRCA-EU 11 70260119 70260119 single base substitution C T downstream_gene_variant BRCA-EU 11 70260119 70260119 single base substitution C T intron_variant BRCA-EU 11 70260119 70260119 single base substitution C T upstream_gene_variant BRCA-EU 11 70261561 70261561 single base substitution C A intron_variant BRCA-EU 11 70261561 70261561 single base substitution C A upstream_gene_variant BRCA-EU 11 70262325 70262325 single base substitution C G downstream_gene_variant BRCA-EU 11 70262325 70262325 single base substitution C G intron_variant BRCA-EU 11 70262325 70262325 single base substitution C G upstream_gene_variant BRCA-EU 11 70262663 70262663 single base substitution A G downstream_gene_variant BRCA-EU 11 70262663 70262663 single base substitution A G intron_variant BRCA-EU 11 70262663 70262663 single base substitution A G upstream_gene_variant BRCA-EU 11 70263946 70263946 single base substitution C A downstream_gene_variant BRCA-EU 11 70263946 70263946 single base substitution C A intron_variant BRCA-EU 11 70263946 70263946 single base substitution C A upstream_gene_variant BRCA-EU 11 70264564 70264564 single base substitution C G downstream_gene_variant BRCA-EU 11 70264564 70264564 single base substitution C G intron_variant BRCA-EU 11 70264564 70264564 single base substitution C G upstream_gene_variant BRCA-EU 11 70264631 70264631 single base substitution G C downstream_gene_variant BRCA-EU 11 70264631 70264631 single base substitution G C intron_variant BRCA-EU 11 70264631 70264631 single base substitution G C upstream_gene_variant BRCA-EU 11 70265072 70265072 single base substitution G A downstream_gene_variant BRCA-EU 11 70265072 70265072 single base substitution G A intron_variant BRCA-EU 11 70265072 70265072 single base substitution G A upstream_gene_variant BRCA-EU 11 70265193 70265193 single base substitution T A downstream_gene_variant BRCA-EU 11 70265193 70265193 single base substitution T A intron_variant BRCA-EU 11 70265193 70265193 single base substitution T A upstream_gene_variant BRCA-EU 11 70265851 70265851 single base substitution G C downstream_gene_variant BRCA-EU 11 70265851 70265851 single base substitution G C splice_acceptor_variant BRCA-EU 11 70265851 70265851 single base substitution G C upstream_gene_variant BRCA-EU 11 70266279 70266279 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 70266279 70266279 single base substitution G C 5_prime_UTR_variant BRCA-EU 11 70266279 70266279 single base substitution G C downstream_gene_variant BRCA-EU 11 70266279 70266279 single base substitution G C intron_variant BRCA-EU 11 70266279 70266279 single base substitution G C upstream_gene_variant BRCA-EU 11 70266333 70266333 single base substitution C A 3_prime_UTR_variant BRCA-EU 11 70266333 70266333 single base substitution C A 5_prime_UTR_variant BRCA-EU 11 70266333 70266333 single base substitution C A downstream_gene_variant BRCA-EU 11 70266333 70266333 single base substitution C A exon_variant BRCA-EU 11 70266333 70266333 single base substitution C A intron_variant BRCA-EU 11 70266333 70266333 single base substitution C A upstream_gene_variant BRCA-EU 11 70267288 70267288 single base substitution G C downstream_gene_variant BRCA-EU 11 70267288 70267288 single base substitution G C intron_variant BRCA-EU 11 70267288 70267288 single base substitution G C upstream_gene_variant BRCA-EU 11 70267633 70267633 single base substitution C T downstream_gene_variant BRCA-EU 11 70267633 70267633 single base substitution C T exon_variant BRCA-EU 11 70267633 70267633 single base substitution C T intron_variant BRCA-EU 11 70267633 70267633 single base substitution C T missense_variant A283V 848C>T BRCA-EU 11 70267633 70267633 single base substitution C T upstream_gene_variant BRCA-EU 11 70268223 70268223 single base substitution G A downstream_gene_variant BRCA-EU 11 70268223 70268223 single base substitution G A exon_variant BRCA-EU 11 70268223 70268223 single base substitution G A intron_variant BRCA-EU 11 70268223 70268223 single base substitution G A upstream_gene_variant BRCA-EU 11 70270468 70270468 single base substitution G C downstream_gene_variant BRCA-EU 11 70270468 70270468 single base substitution G C intron_variant BRCA-EU 11 70270468 70270468 single base substitution G C upstream_gene_variant BRCA-EU 11 70272310 70272310 single base substitution G A downstream_gene_variant BRCA-EU 11 70272310 70272310 single base substitution G A intron_variant BRCA-EU 11 70272310 70272310 single base substitution G A upstream_gene_variant BRCA-EU 11 70272531 70272531 single base substitution A G downstream_gene_variant BRCA-EU 11 70272531 70272531 single base substitution A G intron_variant BRCA-EU 11 70272531 70272531 single base substitution A G upstream_gene_variant BRCA-EU 11 70272974 70272974 single base substitution G C downstream_gene_variant BRCA-EU 11 70272974 70272974 single base substitution G C intron_variant BRCA-EU 11 70272974 70272974 single base substitution G C upstream_gene_variant BRCA-EU 11 70276122 70276122 single base substitution T C downstream_gene_variant BRCA-EU 11 70276122 70276122 single base substitution T C intron_variant BRCA-EU 11 70276665 70276665 single base substitution A G downstream_gene_variant BRCA-EU 11 70276665 70276665 single base substitution A G intron_variant BRCA-EU 11 70277497 70277497 single base substitution A T downstream_gene_variant BRCA-EU 11 70277497 70277497 single base substitution A T intron_variant BRCA-EU 11 70278090 70278090 single base substitution G A downstream_gene_variant BRCA-EU 11 70278090 70278090 single base substitution G A intron_variant BRCA-EU 11 70279105 70279105 single base substitution G T downstream_gene_variant BRCA-EU 11 70279105 70279105 single base substitution G T intron_variant BRCA-EU 11 70279259 70279259 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 70279259 70279259 single base substitution C T downstream_gene_variant BRCA-EU 11 70279259 70279259 single base substitution C T exon_variant BRCA-EU 11 70279259 70279259 single base substitution C T missense_variant T124M 371C>T BRCA-EU 11 70279259 70279259 single base substitution C T missense_variant T403M 1208C>T BRCA-EU 11 70279259 70279259 single base substitution C T missense_variant T440M 1319C>T BRCA-EU 11 70279259 70279259 single base substitution C T missense_variant T97M 290C>T BRCA-EU 11 70280769 70280769 single base substitution C G intron_variant BRCA-EU 11 70281584 70281584 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 70281584 70281584 single base substitution C T downstream_gene_variant BRCA-EU 11 70281584 70281584 single base substitution C T synonymous_variant L198L 594C>T BRCA-EU 11 70281584 70281584 single base substitution C T synonymous_variant L225L 675C>T BRCA-EU 11 70281584 70281584 single base substitution C T synonymous_variant L504L 1512C>T BRCA-EU 11 70281659 70281659 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 70281659 70281659 single base substitution C G downstream_gene_variant BRCA-EU 11 70281659 70281659 single base substitution C G splice_region_variant BRCA-EU 11 70281659 70281659 single base substitution C G synonymous_variant L250L 750C>G BRCA-EU 11 70281659 70281659 single base substitution C G synonymous_variant L529L 1587C>G BRCA-EU 11 70283214 70283214 single base substitution C G downstream_gene_variant BRCA-EU 11 70283683 70283683 single base substitution G C downstream_gene_variant BRCA-EU 11 70284127 70284127 single base substitution G A downstream_gene_variant BRCA-EU 11 70285043 70285043 single base substitution C T downstream_gene_variant BRCA-EU 11 70285269 70285269 single base substitution A T downstream_gene_variant BRCA-EU 11 70286485 70286485 single base substitution G C downstream_gene_variant BRCA-FR 11 70254156 70254156 single base substitution G A exon_variant BRCA-FR 11 70254156 70254156 single base substitution G A intron_variant BRCA-FR 11 70262853 70262853 single base substitution C G downstream_gene_variant BRCA-FR 11 70262853 70262853 single base substitution C G exon_variant BRCA-FR 11 70262853 70262853 single base substitution C G intron_variant BRCA-FR 11 70262853 70262853 single base substitution C G upstream_gene_variant BRCA-FR 11 70267288 70267288 single base substitution G C downstream_gene_variant BRCA-FR 11 70267288 70267288 single base substitution G C intron_variant BRCA-FR 11 70267288 70267288 single base substitution G C upstream_gene_variant BRCA-FR 11 70268223 70268223 single base substitution G A downstream_gene_variant BRCA-FR 11 70268223 70268223 single base substitution G A exon_variant BRCA-FR 11 70268223 70268223 single base substitution G A intron_variant BRCA-FR 11 70268223 70268223 single base substitution G A upstream_gene_variant BRCA-FR 11 70269547 70269547 single base substitution C T downstream_gene_variant BRCA-FR 11 70269547 70269547 single base substitution C T intron_variant BRCA-FR 11 70269607 70269607 single base substitution T C downstream_gene_variant BRCA-FR 11 70269607 70269607 single base substitution T C intron_variant BRCA-FR 11 70285043 70285043 single base substitution C T downstream_gene_variant BRCA-FR 11 70286485 70286485 single base substitution G C downstream_gene_variant BRCA-FR 11 70286588 70286588 single base substitution G T downstream_gene_variant BRCA-FR 11 70286636 70286636 single base substitution G C downstream_gene_variant BRCA-FR 11 70286678 70286678 single base substitution G C downstream_gene_variant BRCA-UK 11 70257341 70257341 single base substitution T A downstream_gene_variant BRCA-UK 11 70257341 70257341 single base substitution T A intron_variant BRCA-UK 11 70257341 70257341 single base substitution T A upstream_gene_variant BRCA-UK 11 70277114 70277114 single base substitution G A downstream_gene_variant BRCA-UK 11 70277114 70277114 single base substitution G A intron_variant BRCA-UK 11 70277207 70277207 single base substitution G C downstream_gene_variant BRCA-UK 11 70277207 70277207 single base substitution G C intron_variant BRCA-UK 11 70277354 70277354 single base substitution G A 3_prime_UTR_variant BRCA-UK 11 70277354 70277354 single base substitution G A downstream_gene_variant BRCA-UK 11 70277354 70277354 single base substitution G A exon_variant BRCA-UK 11 70277354 70277354 single base substitution G A missense_variant E375K 1123G>A BRCA-UK 11 70277354 70277354 single base substitution G A missense_variant E412K 1234G>A BRCA-UK 11 70277354 70277354 single base substitution G A missense_variant E69K 205G>A BRCA-UK 11 70277354 70277354 single base substitution G A missense_variant E96K 286G>A BRCA-UK 11 70277432 70277432 single base substitution G C downstream_gene_variant BRCA-UK 11 70277432 70277432 single base substitution G C intron_variant BRCA-UK 11 70279788 70279788 single base substitution G C 3_prime_UTR_variant BRCA-UK 11 70279788 70279788 single base substitution G C downstream_gene_variant BRCA-UK 11 70279788 70279788 single base substitution G C missense_variant G151R 451G>C BRCA-UK 11 70279788 70279788 single base substitution G C missense_variant G178R 532G>C BRCA-UK 11 70279788 70279788 single base substitution G C missense_variant G457R 1369G>C BRCA-UK 11 70279788 70279788 single base substitution G C missense_variant G494R 1480G>C BRCA-US 11 70256029 70256029 single base substitution G C downstream_gene_variant BRCA-US 11 70256029 70256029 single base substitution G C exon_variant BRCA-US 11 70256029 70256029 single base substitution G C missense_variant G66A 197G>C BRCA-US 11 70256029 70256029 single base substitution G C missense_variant G85A 254G>C BRCA-US 11 70256029 70256029 single base substitution G C upstream_gene_variant BRCA-US 11 70279792 70279792 single base substitution T G 3_prime_UTR_variant BRCA-US 11 70279792 70279792 single base substitution T G downstream_gene_variant BRCA-US 11 70279792 70279792 single base substitution T G missense_variant I152S 455T>G BRCA-US 11 70279792 70279792 single base substitution T G missense_variant I179S 536T>G BRCA-US 11 70279792 70279792 single base substitution T G missense_variant I458S 1373T>G BRCA-US 11 70279792 70279792 single base substitution T G missense_variant I495S 1484T>G BTCA-JP 11 70260677 70260677 single base substitution A G downstream_gene_variant BTCA-JP 11 70260677 70260677 single base substitution A G synonymous_variant K107K 321A>G BTCA-JP 11 70260677 70260677 single base substitution A G synonymous_variant K88K 264A>G BTCA-JP 11 70260677 70260677 single base substitution A G upstream_gene_variant BTCA-JP 11 70261744 70261744 single base substitution T C intron_variant BTCA-JP 11 70261744 70261744 single base substitution T C upstream_gene_variant BTCA-JP 11 70261857 70261857 single base substitution C T exon_variant BTCA-JP 11 70261857 70261857 single base substitution C T intron_variant BTCA-JP 11 70261857 70261857 single base substitution C T upstream_gene_variant BTCA-JP 11 70265914 70265914 single base substitution G A downstream_gene_variant BTCA-JP 11 70265914 70265914 single base substitution G A exon_variant BTCA-JP 11 70265914 70265914 single base substitution G A missense_variant V192I 574G>A BTCA-JP 11 70265914 70265914 single base substitution G A missense_variant V211I 631G>A BTCA-JP 11 70265914 70265914 single base substitution G A upstream_gene_variant BTCA-JP 11 70266470 70266470 deletion of <=200bp T - 5_prime_UTR_variant BTCA-JP 11 70266470 70266470 deletion of <=200bp T - downstream_gene_variant BTCA-JP 11 70266470 70266470 deletion of <=200bp T - exon_variant BTCA-JP 11 70266470 70266470 deletion of <=200bp T - intron_variant BTCA-JP 11 70266470 70266470 deletion of <=200bp T - upstream_gene_variant BTCA-JP 11 70266513 70266513 single base substitution G C 5_prime_UTR_variant BTCA-JP 11 70266513 70266513 single base substitution G C downstream_gene_variant BTCA-JP 11 70266513 70266513 single base substitution G C exon_variant BTCA-JP 11 70266513 70266513 single base substitution G C synonymous_variant V229V 687G>C BTCA-JP 11 70266513 70266513 single base substitution G C upstream_gene_variant BTCA-JP 11 70268540 70268540 single base substitution G A downstream_gene_variant BTCA-JP 11 70268540 70268540 single base substitution G A exon_variant BTCA-JP 11 70268540 70268540 single base substitution G A intron_variant BTCA-JP 11 70268540 70268540 single base substitution G A upstream_gene_variant BTCA-JP 11 70268693 70268693 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BTCA-JP 11 70268693 70268693 single base substitution G A downstream_gene_variant BTCA-JP 11 70268693 70268693 single base substitution G A exon_variant BTCA-JP 11 70268693 70268693 single base substitution G A intron_variant CESC-US 11 70275181 70275181 single base substitution G C 3_prime_UTR_variant CESC-US 11 70275181 70275181 single base substitution G C downstream_gene_variant CESC-US 11 70275181 70275181 single base substitution G C missense_variant R314T 941G>C CESC-US 11 70275181 70275181 single base substitution G C missense_variant R351T 1052G>C CESC-US 11 70275181 70275181 single base substitution G C missense_variant R35T 104G>C CESC-US 11 70275181 70275181 single base substitution G C missense_variant R8T 23G>C CESC-US 11 70275181 70275181 single base substitution G C upstream_gene_variant CLLE-ES 11 70250977 70250977 single base substitution G A intron_variant CLLE-ES 11 70250977 70250977 single base substitution G A upstream_gene_variant CLLE-ES 11 70251018 70251018 single base substitution G T intron_variant CLLE-ES 11 70251018 70251018 single base substitution G T upstream_gene_variant CLLE-ES 11 70252647 70252647 single base substitution A T intron_variant CLLE-ES 11 70252647 70252647 single base substitution A T upstream_gene_variant CLLE-ES 11 70260778 70260778 single base substitution G T downstream_gene_variant CLLE-ES 11 70260778 70260778 single base substitution G T intron_variant CLLE-ES 11 70260778 70260778 single base substitution G T upstream_gene_variant CLLE-ES 11 70273567 70273567 single base substitution G T downstream_gene_variant CLLE-ES 11 70273567 70273567 single base substitution G T intron_variant CLLE-ES 11 70273567 70273567 single base substitution G T upstream_gene_variant COAD-US 11 70253451 70253451 single base substitution C T exon_variant COAD-US 11 70253451 70253451 single base substitution C T synonymous_variant D16D 48C>T COAD-US 11 70253451 70253451 single base substitution C T upstream_gene_variant COAD-US 11 70253475 70253475 single base substitution C T exon_variant COAD-US 11 70253475 70253475 single base substitution C T synonymous_variant T24T 72C>T COAD-US 11 70253475 70253475 single base substitution C T synonymous_variant T5T 15C>T COAD-US 11 70260715 70260715 single base substitution G T downstream_gene_variant COAD-US 11 70260715 70260715 single base substitution G T missense_variant G101V 302G>T COAD-US 11 70260715 70260715 single base substitution G T missense_variant G120V 359G>T COAD-US 11 70260715 70260715 single base substitution G T upstream_gene_variant COAD-US 11 70260753 70260753 single base substitution G T downstream_gene_variant COAD-US 11 70260753 70260753 single base substitution G T exon_variant COAD-US 11 70260753 70260753 single base substitution G T missense_variant D114Y 340G>T COAD-US 11 70260753 70260753 single base substitution G T missense_variant D133Y 397G>T COAD-US 11 70260753 70260753 single base substitution G T upstream_gene_variant COAD-US 11 70263207 70263207 single base substitution G A downstream_gene_variant COAD-US 11 70263207 70263207 single base substitution G A exon_variant COAD-US 11 70263207 70263207 single base substitution G A synonymous_variant T163T 489G>A COAD-US 11 70263207 70263207 single base substitution G A synonymous_variant T182T 546G>A COAD-US 11 70263207 70263207 single base substitution G A upstream_gene_variant COAD-US 11 70277323 70277323 single base substitution G A 3_prime_UTR_variant COAD-US 11 70277323 70277323 single base substitution G A downstream_gene_variant COAD-US 11 70277323 70277323 single base substitution G A exon_variant COAD-US 11 70277323 70277323 single base substitution G A synonymous_variant T364T 1092G>A COAD-US 11 70277323 70277323 single base substitution G A synonymous_variant T401T 1203G>A COAD-US 11 70277323 70277323 single base substitution G A synonymous_variant T58T 174G>A COAD-US 11 70277323 70277323 single base substitution G A synonymous_variant T85T 255G>A COAD-US 11 70281208 70281208 single base substitution C T 3_prime_UTR_variant COAD-US 11 70281208 70281208 single base substitution C T synonymous_variant R188R 564C>T COAD-US 11 70281208 70281208 single base substitution C T synonymous_variant R215R 645C>T COAD-US 11 70281208 70281208 single base substitution C T synonymous_variant R494R 1482C>T COAD-US 11 70281208 70281208 single base substitution C T synonymous_variant R531R 1593C>T COCA-CN 11 70249762 70249762 single base substitution A T intron_variant COCA-CN 11 70249762 70249762 single base substitution A T upstream_gene_variant COCA-CN 11 70255911 70255911 single base substitution T G downstream_gene_variant COCA-CN 11 70255911 70255911 single base substitution T G intron_variant COCA-CN 11 70255911 70255911 single base substitution T G upstream_gene_variant COCA-CN 11 70256020 70256020 single base substitution A G downstream_gene_variant COCA-CN 11 70256020 70256020 single base substitution A G exon_variant COCA-CN 11 70256020 70256020 single base substitution A G missense_variant H63R 188A>G COCA-CN 11 70256020 70256020 single base substitution A G missense_variant H82R 245A>G COCA-CN 11 70256020 70256020 single base substitution A G upstream_gene_variant COCA-CN 11 70260760 70260760 single base substitution T C downstream_gene_variant COCA-CN 11 70260760 70260760 single base substitution T C splice_donor_variant COCA-CN 11 70260760 70260760 single base substitution T C upstream_gene_variant COCA-CN 11 70265811 70265811 single base substitution C T downstream_gene_variant COCA-CN 11 70265811 70265811 single base substitution C T intron_variant COCA-CN 11 70265811 70265811 single base substitution C T upstream_gene_variant COCA-CN 11 70268910 70268910 single base substitution C T downstream_gene_variant COCA-CN 11 70268910 70268910 single base substitution C T exon_variant COCA-CN 11 70268910 70268910 single base substitution C T intron_variant COCA-CN 11 70269152 70269152 single base substitution G T downstream_gene_variant COCA-CN 11 70269152 70269152 single base substitution G T intron_variant COCA-CN 11 70279927 70279927 single base substitution G A downstream_gene_variant COCA-CN 11 70279927 70279927 single base substitution G A intron_variant COCA-CN 11 70282360 70282360 single base substitution C A 3_prime_UTR_variant COCA-CN 11 70282360 70282360 single base substitution C A downstream_gene_variant COCA-CN 11 70282360 70282360 single base substitution C A intron_variant EOPC-DE 11 70265987 70265987 single base substitution C A downstream_gene_variant EOPC-DE 11 70265987 70265987 single base substitution C A intron_variant EOPC-DE 11 70265987 70265987 single base substitution C A missense_variant S216Y 647C>A EOPC-DE 11 70265987 70265987 single base substitution C A upstream_gene_variant ESAD-UK 11 70239834 70239834 single base substitution G C upstream_gene_variant ESAD-UK 11 70239898 70239898 single base substitution T G upstream_gene_variant ESAD-UK 11 70239990 70239990 single base substitution G C upstream_gene_variant ESAD-UK 11 70240031 70240031 single base substitution G A upstream_gene_variant ESAD-UK 11 70240089 70240089 single base substitution G A upstream_gene_variant ESAD-UK 11 70240137 70240137 single base substitution G C upstream_gene_variant ESAD-UK 11 70240323 70240323 single base substitution G T upstream_gene_variant ESAD-UK 11 70240446 70240446 single base substitution C T upstream_gene_variant ESAD-UK 11 70241162 70241162 single base substitution C T upstream_gene_variant ESAD-UK 11 70241768 70241768 single base substitution G C upstream_gene_variant ESAD-UK 11 70243126 70243126 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 70244539 70244539 single base substitution C T 5_prime_UTR_variant ESAD-UK 11 70244539 70244539 single base substitution C T upstream_gene_variant ESAD-UK 11 70247508 70247508 single base substitution C T intron_variant ESAD-UK 11 70248885 70248885 single base substitution T G intron_variant ESAD-UK 11 70248885 70248885 single base substitution T G upstream_gene_variant ESAD-UK 11 70252344 70252344 single base substitution C T intron_variant ESAD-UK 11 70252344 70252344 single base substitution C T upstream_gene_variant ESAD-UK 11 70255141 70255141 single base substitution A G downstream_gene_variant ESAD-UK 11 70255141 70255141 single base substitution A G intron_variant ESAD-UK 11 70255195 70255195 single base substitution C T downstream_gene_variant ESAD-UK 11 70255195 70255195 single base substitution C T intron_variant ESAD-UK 11 70255281 70255281 single base substitution C T downstream_gene_variant ESAD-UK 11 70255281 70255281 single base substitution C T intron_variant ESAD-UK 11 70256178 70256178 single base substitution G C downstream_gene_variant ESAD-UK 11 70256178 70256178 single base substitution G C intron_variant ESAD-UK 11 70256178 70256178 single base substitution G C upstream_gene_variant ESAD-UK 11 70258185 70258185 single base substitution C T downstream_gene_variant ESAD-UK 11 70258185 70258185 single base substitution C T intron_variant ESAD-UK 11 70258185 70258185 single base substitution C T upstream_gene_variant ESAD-UK 11 70260427 70260427 single base substitution G A downstream_gene_variant ESAD-UK 11 70260427 70260427 single base substitution G A intron_variant ESAD-UK 11 70260427 70260427 single base substitution G A upstream_gene_variant ESAD-UK 11 70260813 70260813 single base substitution G A downstream_gene_variant ESAD-UK 11 70260813 70260813 single base substitution G A intron_variant ESAD-UK 11 70260813 70260813 single base substitution G A upstream_gene_variant ESAD-UK 11 70262295 70262295 single base substitution G A exon_variant ESAD-UK 11 70262295 70262295 single base substitution G A intron_variant ESAD-UK 11 70262295 70262295 single base substitution G A upstream_gene_variant ESAD-UK 11 70264271 70264271 single base substitution G A downstream_gene_variant ESAD-UK 11 70264271 70264271 single base substitution G A intron_variant ESAD-UK 11 70264271 70264271 single base substitution G A upstream_gene_variant ESAD-UK 11 70265291 70265291 single base substitution A G downstream_gene_variant ESAD-UK 11 70265291 70265291 single base substitution A G intron_variant ESAD-UK 11 70265291 70265291 single base substitution A G upstream_gene_variant ESAD-UK 11 70268223 70268223 single base substitution G A downstream_gene_variant ESAD-UK 11 70268223 70268223 single base substitution G A exon_variant ESAD-UK 11 70268223 70268223 single base substitution G A intron_variant ESAD-UK 11 70268223 70268223 single base substitution G A upstream_gene_variant ESAD-UK 11 70268746 70268746 single base substitution G A downstream_gene_variant ESAD-UK 11 70268746 70268746 single base substitution G A exon_variant ESAD-UK 11 70268746 70268746 single base substitution G A intron_variant ESAD-UK 11 70269337 70269337 single base substitution C T downstream_gene_variant ESAD-UK 11 70269337 70269337 single base substitution C T intron_variant ESAD-UK 11 70269380 70269380 single base substitution G A downstream_gene_variant ESAD-UK 11 70269380 70269380 single base substitution G A intron_variant ESAD-UK 11 70270063 70270063 single base substitution C T downstream_gene_variant ESAD-UK 11 70270063 70270063 single base substitution C T intron_variant ESAD-UK 11 70275255 70275255 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 70275255 70275255 single base substitution C T downstream_gene_variant ESAD-UK 11 70275255 70275255 single base substitution C T exon_variant ESAD-UK 11 70275255 70275255 single base substitution C T missense_variant R339W 1015C>T ESAD-UK 11 70275255 70275255 single base substitution C T missense_variant R33W 97C>T ESAD-UK 11 70275255 70275255 single base substitution C T missense_variant R376W 1126C>T ESAD-UK 11 70275255 70275255 single base substitution C T missense_variant R60W 178C>T ESAD-UK 11 70276097 70276097 single base substitution C T downstream_gene_variant ESAD-UK 11 70276097 70276097 single base substitution C T intron_variant ESAD-UK 11 70276531 70276531 single base substitution T G downstream_gene_variant ESAD-UK 11 70276531 70276531 single base substitution T G intron_variant ESAD-UK 11 70277527 70277527 single base substitution G A downstream_gene_variant ESAD-UK 11 70277527 70277527 single base substitution G A intron_variant ESAD-UK 11 70279154 70279154 single base substitution C A downstream_gene_variant ESAD-UK 11 70279154 70279154 single base substitution C A intron_variant ESAD-UK 11 70279301 70279301 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 70279301 70279301 single base substitution G A downstream_gene_variant ESAD-UK 11 70279301 70279301 single base substitution G A exon_variant ESAD-UK 11 70279301 70279301 single base substitution G A missense_variant R111Q 332G>A ESAD-UK 11 70279301 70279301 single base substitution G A missense_variant R138Q 413G>A ESAD-UK 11 70279301 70279301 single base substitution G A missense_variant R417Q 1250G>A ESAD-UK 11 70279301 70279301 single base substitution G A missense_variant R454Q 1361G>A ESAD-UK 11 70279378 70279378 single base substitution C G 3_prime_UTR_variant ESAD-UK 11 70279378 70279378 single base substitution C G downstream_gene_variant ESAD-UK 11 70279378 70279378 single base substitution C G exon_variant ESAD-UK 11 70279378 70279378 single base substitution C G missense_variant P137A 409C>G ESAD-UK 11 70279378 70279378 single base substitution C G missense_variant P164A 490C>G ESAD-UK 11 70279378 70279378 single base substitution C G missense_variant P443A 1327C>G ESAD-UK 11 70279378 70279378 single base substitution C G missense_variant P480A 1438C>G ESAD-UK 11 70279560 70279560 single base substitution G T downstream_gene_variant ESAD-UK 11 70279560 70279560 single base substitution G T intron_variant ESAD-UK 11 70280447 70280447 single base substitution C T intron_variant ESAD-UK 11 70281000 70281000 single base substitution G A intron_variant ESAD-UK 11 70282670 70282670 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 11 70282670 70282670 deletion of <=200bp T - downstream_gene_variant ESAD-UK 11 70283120 70283120 single base substitution A G downstream_gene_variant ESAD-UK 11 70285835 70285835 single base substitution T A downstream_gene_variant ESCA-CN 11 70281607 70281607 single base substitution C G 3_prime_UTR_variant ESCA-CN 11 70281607 70281607 single base substitution C G downstream_gene_variant ESCA-CN 11 70281607 70281607 single base substitution C G missense_variant A206G 617C>G ESCA-CN 11 70281607 70281607 single base substitution C G missense_variant A233G 698C>G ESCA-CN 11 70281607 70281607 single base substitution C G missense_variant A512G 1535C>G ESCA-CN 11 70281724 70281724 single base substitution C T 3_prime_UTR_variant ESCA-CN 11 70281724 70281724 single base substitution C T downstream_gene_variant ESCA-CN 11 70281724 70281724 single base substitution C T intron_variant ESCA-CN 11 70281724 70281724 single base substitution C T missense_variant S272L 815C>T ESCA-CN 11 70281724 70281724 single base substitution C T missense_variant S551L 1652C>T GBM-US 11 70255986 70255986 single base substitution G A downstream_gene_variant GBM-US 11 70255986 70255986 single base substitution G A exon_variant GBM-US 11 70255986 70255986 single base substitution G A missense_variant E52K 154G>A GBM-US 11 70255986 70255986 single base substitution G A missense_variant E71K 211G>A GBM-US 11 70255986 70255986 single base substitution G A upstream_gene_variant GBM-US 11 70266538 70266538 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant GBM-US 11 70266538 70266538 single base substitution G A downstream_gene_variant GBM-US 11 70266538 70266538 single base substitution G A exon_variant GBM-US 11 70266538 70266538 single base substitution G A missense_variant V238M 712G>A GBM-US 11 70266538 70266538 single base substitution G A upstream_gene_variant GBM-US 11 70279266 70279266 single base substitution G A 3_prime_UTR_variant GBM-US 11 70279266 70279266 single base substitution G A downstream_gene_variant GBM-US 11 70279266 70279266 single base substitution G A exon_variant GBM-US 11 70279266 70279266 single base substitution G A synonymous_variant P126P 378G>A GBM-US 11 70279266 70279266 single base substitution G A synonymous_variant P405P 1215G>A GBM-US 11 70279266 70279266 single base substitution G A synonymous_variant P442P 1326G>A GBM-US 11 70279266 70279266 single base substitution G A synonymous_variant P99P 297G>A LAML-KR 11 70257290 70257290 single base substitution A G downstream_gene_variant LAML-KR 11 70257290 70257290 single base substitution A G intron_variant LAML-KR 11 70257290 70257290 single base substitution A G upstream_gene_variant LAML-KR 11 70257291 70257291 single base substitution A T downstream_gene_variant LAML-KR 11 70257291 70257291 single base substitution A T intron_variant LAML-KR 11 70257291 70257291 single base substitution A T upstream_gene_variant LAML-KR 11 70257539 70257539 single base substitution T A downstream_gene_variant LAML-KR 11 70257539 70257539 single base substitution T A intron_variant LAML-KR 11 70257539 70257539 single base substitution T A upstream_gene_variant LAML-KR 11 70282004 70282004 single base substitution C A 3_prime_UTR_variant LAML-KR 11 70282004 70282004 single base substitution C A downstream_gene_variant LAML-KR 11 70282004 70282004 single base substitution C A intron_variant LGG-US 11 70261803 70261803 single base substitution A G exon_variant LGG-US 11 70261803 70261803 single base substitution A G missense_variant E127G 380A>G LGG-US 11 70261803 70261803 single base substitution A G missense_variant E146G 437A>G LGG-US 11 70261803 70261803 single base substitution A G upstream_gene_variant LICA-CN 11 70253472 70253472 single base substitution G A exon_variant LICA-CN 11 70253472 70253472 single base substitution G A synonymous_variant E23E 69G>A LICA-CN 11 70253472 70253472 single base substitution G A synonymous_variant E4E 12G>A LICA-FR 11 70263630 70263630 single base substitution C T downstream_gene_variant LICA-FR 11 70263630 70263630 single base substitution C T intron_variant LICA-FR 11 70263630 70263630 single base substitution C T upstream_gene_variant LICA-FR 11 70279341 70279341 single base substitution G A 3_prime_UTR_variant LICA-FR 11 70279341 70279341 single base substitution G A downstream_gene_variant LICA-FR 11 70279341 70279341 single base substitution G A exon_variant LICA-FR 11 70279341 70279341 single base substitution G A synonymous_variant E124E 372G>A LICA-FR 11 70279341 70279341 single base substitution G A synonymous_variant E151E 453G>A LICA-FR 11 70279341 70279341 single base substitution G A synonymous_variant E430E 1290G>A LICA-FR 11 70279341 70279341 single base substitution G A synonymous_variant E467E 1401G>A LIHC-US 11 70260723 70260723 single base substitution G A downstream_gene_variant LIHC-US 11 70260723 70260723 single base substitution G A exon_variant LIHC-US 11 70260723 70260723 single base substitution G A missense_variant G104S 310G>A LIHC-US 11 70260723 70260723 single base substitution G A missense_variant G123S 367G>A LIHC-US 11 70260723 70260723 single base substitution G A upstream_gene_variant LIHC-US 11 70269063 70269063 single base substitution G A 5_prime_UTR_variant LIHC-US 11 70269063 70269063 single base substitution G A downstream_gene_variant LIHC-US 11 70269063 70269063 single base substitution G A exon_variant LIHC-US 11 70269063 70269063 single base substitution G A missense_variant G270S 808G>A LIHC-US 11 70269063 70269063 single base substitution G A missense_variant G307S 919G>A LINC-JP 11 70254252 70254252 single base substitution G C exon_variant LINC-JP 11 70254252 70254252 single base substitution G C intron_variant LINC-JP 11 70260755 70260755 single base substitution T A downstream_gene_variant LINC-JP 11 70260755 70260755 single base substitution T A exon_variant LINC-JP 11 70260755 70260755 single base substitution T A missense_variant D114E 342T>A LINC-JP 11 70260755 70260755 single base substitution T A missense_variant D133E 399T>A LINC-JP 11 70260755 70260755 single base substitution T A upstream_gene_variant LINC-JP 11 70260756 70260756 single base substitution C A downstream_gene_variant LINC-JP 11 70260756 70260756 single base substitution C A missense_variant Q115K 343C>A LINC-JP 11 70260756 70260756 single base substitution C A missense_variant Q134K 400C>A LINC-JP 11 70260756 70260756 single base substitution C A splice_region_variant LINC-JP 11 70260756 70260756 single base substitution C A upstream_gene_variant LINC-JP 11 70261300 70261300 single base substitution C T downstream_gene_variant LINC-JP 11 70261300 70261300 single base substitution C T intron_variant LINC-JP 11 70261300 70261300 single base substitution C T upstream_gene_variant LINC-JP 11 70261919 70261919 single base substitution T C exon_variant LINC-JP 11 70261919 70261919 single base substitution T C intron_variant LINC-JP 11 70261919 70261919 single base substitution T C upstream_gene_variant LINC-JP 11 70266538 70266538 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 11 70266538 70266538 single base substitution G T downstream_gene_variant LINC-JP 11 70266538 70266538 single base substitution G T exon_variant LINC-JP 11 70266538 70266538 single base substitution G T missense_variant V238L 712G>T LINC-JP 11 70266538 70266538 single base substitution G T upstream_gene_variant LINC-JP 11 70280916 70280916 single base substitution A G intron_variant LIRI-JP 11 70239866 70239866 single base substitution G A upstream_gene_variant LIRI-JP 11 70251181 70251181 single base substitution T G intron_variant LIRI-JP 11 70251181 70251181 single base substitution T G upstream_gene_variant LIRI-JP 11 70257977 70257977 single base substitution C A downstream_gene_variant LIRI-JP 11 70257977 70257977 single base substitution C A intron_variant LIRI-JP 11 70257977 70257977 single base substitution C A upstream_gene_variant LIRI-JP 11 70258254 70258254 single base substitution C A downstream_gene_variant LIRI-JP 11 70258254 70258254 single base substitution C A intron_variant LIRI-JP 11 70258254 70258254 single base substitution C A upstream_gene_variant LIRI-JP 11 70259048 70259048 single base substitution C T downstream_gene_variant LIRI-JP 11 70259048 70259048 single base substitution C T intron_variant LIRI-JP 11 70259048 70259048 single base substitution C T upstream_gene_variant LIRI-JP 11 70263160 70263160 single base substitution G A downstream_gene_variant LIRI-JP 11 70263160 70263160 single base substitution G A exon_variant LIRI-JP 11 70263160 70263160 single base substitution G A missense_variant D148N 442G>A LIRI-JP 11 70263160 70263160 single base substitution G A missense_variant D167N 499G>A LIRI-JP 11 70263160 70263160 single base substitution G A upstream_gene_variant LIRI-JP 11 70263179 70263179 single base substitution C T downstream_gene_variant LIRI-JP 11 70263179 70263179 single base substitution C T exon_variant LIRI-JP 11 70263179 70263179 single base substitution C T missense_variant A154V 461C>T LIRI-JP 11 70263179 70263179 single base substitution C T missense_variant A173V 518C>T LIRI-JP 11 70263179 70263179 single base substitution C T upstream_gene_variant LIRI-JP 11 70263994 70263994 single base substitution C T downstream_gene_variant LIRI-JP 11 70263994 70263994 single base substitution C T intron_variant LIRI-JP 11 70263994 70263994 single base substitution C T upstream_gene_variant LIRI-JP 11 70267086 70267086 single base substitution A G downstream_gene_variant LIRI-JP 11 70267086 70267086 single base substitution A G intron_variant LIRI-JP 11 70267086 70267086 single base substitution A G upstream_gene_variant LIRI-JP 11 70267767 70267767 single base substitution C A downstream_gene_variant LIRI-JP 11 70267767 70267767 single base substitution C A exon_variant LIRI-JP 11 70267767 70267767 single base substitution C A intron_variant LIRI-JP 11 70267767 70267767 single base substitution C A upstream_gene_variant LIRI-JP 11 70271587 70271587 single base substitution G A downstream_gene_variant LIRI-JP 11 70271587 70271587 single base substitution G A intron_variant LIRI-JP 11 70271587 70271587 single base substitution G A upstream_gene_variant LIRI-JP 11 70274854 70274854 single base substitution A G downstream_gene_variant LIRI-JP 11 70274854 70274854 single base substitution A G intron_variant LIRI-JP 11 70274854 70274854 single base substitution A G upstream_gene_variant LIRI-JP 11 70281127 70281127 single base substitution C A intron_variant LIRI-JP 11 70281127 70281127 single base substitution C A splice_region_variant LIRI-JP 11 70282866 70282866 single base substitution G T downstream_gene_variant LIRI-JP 11 70284265 70284265 single base substitution C T downstream_gene_variant LIRI-JP 11 70284303 70284309 deletion of <=200bp CTGGCCA - downstream_gene_variant LIRI-JP 11 70285138 70285138 single base substitution G T downstream_gene_variant LIRI-JP 11 70286609 70286609 single base substitution C T downstream_gene_variant LIRI-JP 11 70286911 70286911 single base substitution A G downstream_gene_variant LIRI-JP 11 70287167 70287167 single base substitution G A downstream_gene_variant LUSC-KR 11 70247646 70247646 single base substitution C T intron_variant LUSC-KR 11 70252977 70252977 single base substitution A G intron_variant LUSC-KR 11 70252977 70252977 single base substitution A G upstream_gene_variant LUSC-KR 11 70257380 70257380 single base substitution C T downstream_gene_variant LUSC-KR 11 70257380 70257380 single base substitution C T intron_variant LUSC-KR 11 70257380 70257380 single base substitution C T upstream_gene_variant LUSC-KR 11 70257974 70257974 single base substitution C T downstream_gene_variant LUSC-KR 11 70257974 70257974 single base substitution C T intron_variant LUSC-KR 11 70257974 70257974 single base substitution C T upstream_gene_variant LUSC-KR 11 70268734 70268734 single base substitution A T 5_prime_UTR_variant LUSC-KR 11 70268734 70268734 single base substitution A T downstream_gene_variant LUSC-KR 11 70268734 70268734 single base substitution A T exon_variant LUSC-KR 11 70268734 70268734 single base substitution A T intron_variant LUSC-KR 11 70269186 70269186 single base substitution C G downstream_gene_variant LUSC-KR 11 70269186 70269186 single base substitution C G intron_variant LUSC-KR 11 70269706 70269706 single base substitution C T downstream_gene_variant LUSC-KR 11 70269706 70269706 single base substitution C T intron_variant LUSC-KR 11 70272009 70272009 single base substitution C T downstream_gene_variant LUSC-KR 11 70272009 70272009 single base substitution C T intron_variant LUSC-KR 11 70272009 70272009 single base substitution C T upstream_gene_variant LUSC-KR 11 70272373 70272373 single base substitution C T downstream_gene_variant LUSC-KR 11 70272373 70272373 single base substitution C T intron_variant LUSC-KR 11 70272373 70272373 single base substitution C T upstream_gene_variant LUSC-KR 11 70279158 70279158 single base substitution C G downstream_gene_variant LUSC-KR 11 70279158 70279158 single base substitution C G intron_variant LUSC-KR 11 70279927 70279927 single base substitution G A downstream_gene_variant LUSC-KR 11 70279927 70279927 single base substitution G A intron_variant LUSC-KR 11 70285873 70285873 single base substitution G A downstream_gene_variant LUSC-KR 11 70286197 70286197 single base substitution C T downstream_gene_variant LUSC-KR 11 70287652 70287652 single base substitution G T downstream_gene_variant LUSC-US 11 70255985 70255985 single base substitution G T downstream_gene_variant LUSC-US 11 70255985 70255985 single base substitution G T exon_variant LUSC-US 11 70255985 70255985 single base substitution G T missense_variant K51N 153G>T LUSC-US 11 70255985 70255985 single base substitution G T missense_variant K70N 210G>T LUSC-US 11 70255985 70255985 single base substitution G T upstream_gene_variant LUSC-US 11 70260667 70260667 single base substitution A G downstream_gene_variant LUSC-US 11 70260667 70260667 single base substitution A G missense_variant Y104C 311A>G LUSC-US 11 70260667 70260667 single base substitution A G missense_variant Y85C 254A>G LUSC-US 11 70260667 70260667 single base substitution A G upstream_gene_variant LUSC-US 11 70266527 70266527 single base substitution G A 5_prime_UTR_variant LUSC-US 11 70266527 70266527 single base substitution G A downstream_gene_variant LUSC-US 11 70266527 70266527 single base substitution G A exon_variant LUSC-US 11 70266527 70266527 single base substitution G A missense_variant G234E 701G>A LUSC-US 11 70266527 70266527 single base substitution G A upstream_gene_variant LUSC-US 11 70277370 70277370 single base substitution C A 3_prime_UTR_variant LUSC-US 11 70277370 70277370 single base substitution C A downstream_gene_variant LUSC-US 11 70277370 70277370 single base substitution C A exon_variant LUSC-US 11 70277370 70277370 single base substitution C A stop_gained S101* 302C>A LUSC-US 11 70277370 70277370 single base substitution C A stop_gained S380* 1139C>A LUSC-US 11 70277370 70277370 single base substitution C A stop_gained S417* 1250C>A LUSC-US 11 70277370 70277370 single base substitution C A stop_gained S74* 221C>A LUSC-US 11 70281197 70281197 single base substitution G C 3_prime_UTR_variant LUSC-US 11 70281197 70281197 single base substitution G C missense_variant G185R 553G>C LUSC-US 11 70281197 70281197 single base substitution G C missense_variant G212R 634G>C LUSC-US 11 70281197 70281197 single base substitution G C missense_variant G491R 1471G>C LUSC-US 11 70281197 70281197 single base substitution G C missense_variant G528R 1582G>C MALY-DE 11 70244532 70244532 single base substitution C G 5_prime_UTR_variant MALY-DE 11 70244532 70244532 single base substitution C G upstream_gene_variant MALY-DE 11 70245100 70245100 single base substitution G A intron_variant MALY-DE 11 70251109 70251109 insertion of <=200bp - A intron_variant MALY-DE 11 70251109 70251109 insertion of <=200bp - A upstream_gene_variant MALY-DE 11 70251607 70251607 single base substitution C A intron_variant MALY-DE 11 70251607 70251607 single base substitution C A upstream_gene_variant MALY-DE 11 70252651 70252651 single base substitution T A intron_variant MALY-DE 11 70252651 70252651 single base substitution T A upstream_gene_variant MALY-DE 11 70253709 70253709 single base substitution C T exon_variant MALY-DE 11 70253709 70253709 single base substitution C T intron_variant MALY-DE 11 70258309 70258309 single base substitution G A downstream_gene_variant MALY-DE 11 70258309 70258309 single base substitution G A intron_variant MALY-DE 11 70258309 70258309 single base substitution G A upstream_gene_variant MALY-DE 11 70261681 70261681 single base substitution A C intron_variant MALY-DE 11 70261681 70261681 single base substitution A C upstream_gene_variant MALY-DE 11 70266123 70266123 single base substitution C T 3_prime_UTR_variant MALY-DE 11 70266123 70266123 single base substitution C T downstream_gene_variant MALY-DE 11 70266123 70266123 single base substitution C T intron_variant MALY-DE 11 70266123 70266123 single base substitution C T upstream_gene_variant MALY-DE 11 70266443 70266443 single base substitution C G 5_prime_UTR_variant MALY-DE 11 70266443 70266443 single base substitution C G downstream_gene_variant MALY-DE 11 70266443 70266443 single base substitution C G exon_variant MALY-DE 11 70266443 70266443 single base substitution C G intron_variant MALY-DE 11 70266443 70266443 single base substitution C G upstream_gene_variant MALY-DE 11 70267893 70267893 single base substitution G C downstream_gene_variant MALY-DE 11 70267893 70267893 single base substitution G C exon_variant MALY-DE 11 70267893 70267893 single base substitution G C intron_variant MALY-DE 11 70267893 70267893 single base substitution G C upstream_gene_variant MALY-DE 11 70273648 70273648 single base substitution G A downstream_gene_variant MALY-DE 11 70273648 70273648 single base substitution G A intron_variant MALY-DE 11 70273648 70273648 single base substitution G A upstream_gene_variant MALY-DE 11 70280779 70280779 single base substitution C T intron_variant MALY-DE 11 70282646 70282646 single base substitution A T 3_prime_UTR_variant MALY-DE 11 70282646 70282646 single base substitution A T downstream_gene_variant MELA-AU 11 70240488 70240488 single base substitution G A upstream_gene_variant MELA-AU 11 70240627 70240627 single base substitution C T upstream_gene_variant MELA-AU 11 70240914 70240914 single base substitution G A upstream_gene_variant MELA-AU 11 70241098 70241098 single base substitution C T upstream_gene_variant MELA-AU 11 70242004 70242004 single base substitution G A upstream_gene_variant MELA-AU 11 70243957 70243957 single base substitution G A upstream_gene_variant MELA-AU 11 70244203 70244203 single base substitution C T upstream_gene_variant MELA-AU 11 70244388 70244389 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 70244636 70244636 single base substitution G A 5_prime_UTR_variant MELA-AU 11 70244636 70244636 single base substitution G A upstream_gene_variant MELA-AU 11 70244769 70244769 single base substitution T G intron_variant MELA-AU 11 70246419 70246419 single base substitution G A intron_variant MELA-AU 11 70246647 70246647 single base substitution C T intron_variant MELA-AU 11 70247005 70247005 single base substitution G A intron_variant MELA-AU 11 70247829 70247829 single base substitution A T intron_variant MELA-AU 11 70249151 70249151 single base substitution C T intron_variant MELA-AU 11 70249151 70249151 single base substitution C T upstream_gene_variant MELA-AU 11 70249475 70249475 single base substitution C T intron_variant MELA-AU 11 70249475 70249475 single base substitution C T upstream_gene_variant MELA-AU 11 70249661 70249661 single base substitution C T intron_variant MELA-AU 11 70249661 70249661 single base substitution C T upstream_gene_variant MELA-AU 11 70250529 70250529 insertion of <=200bp - AACC intron_variant MELA-AU 11 70250529 70250529 insertion of <=200bp - AACC upstream_gene_variant MELA-AU 11 70250542 70250542 single base substitution C T intron_variant MELA-AU 11 70250542 70250542 single base substitution C T upstream_gene_variant MELA-AU 11 70250867 70250867 single base substitution G A intron_variant MELA-AU 11 70250867 70250867 single base substitution G A upstream_gene_variant MELA-AU 11 70250991 70250991 single base substitution C T intron_variant MELA-AU 11 70250991 70250991 single base substitution C T upstream_gene_variant MELA-AU 11 70251383 70251383 single base substitution C T 5_prime_UTR_variant MELA-AU 11 70251383 70251383 single base substitution C T exon_variant MELA-AU 11 70251383 70251383 single base substitution C T upstream_gene_variant MELA-AU 11 70251452 70251452 single base substitution C T 5_prime_UTR_variant MELA-AU 11 70251452 70251452 single base substitution C T exon_variant MELA-AU 11 70251452 70251452 single base substitution C T upstream_gene_variant MELA-AU 11 70251953 70251953 single base substitution C T intron_variant MELA-AU 11 70251953 70251953 single base substitution C T upstream_gene_variant MELA-AU 11 70252180 70252180 single base substitution C T intron_variant MELA-AU 11 70252180 70252180 single base substitution C T upstream_gene_variant MELA-AU 11 70252664 70252664 single base substitution C T intron_variant MELA-AU 11 70252664 70252664 single base substitution C T upstream_gene_variant MELA-AU 11 70252771 70252771 single base substitution C A intron_variant MELA-AU 11 70252771 70252771 single base substitution C A upstream_gene_variant MELA-AU 11 70253909 70253909 single base substitution C T exon_variant MELA-AU 11 70253909 70253909 single base substitution C T intron_variant MELA-AU 11 70253932 70253932 single base substitution C T exon_variant MELA-AU 11 70253932 70253932 single base substitution C T intron_variant MELA-AU 11 70254106 70254106 single base substitution G A exon_variant MELA-AU 11 70254106 70254106 single base substitution G A intron_variant MELA-AU 11 70254335 70254335 single base substitution C T exon_variant MELA-AU 11 70254335 70254335 single base substitution C T intron_variant MELA-AU 11 70254419 70254419 single base substitution C T exon_variant MELA-AU 11 70254419 70254419 single base substitution C T intron_variant MELA-AU 11 70254519 70254519 single base substitution T C downstream_gene_variant MELA-AU 11 70254519 70254519 single base substitution T C intron_variant MELA-AU 11 70254594 70254594 single base substitution C T downstream_gene_variant MELA-AU 11 70254594 70254594 single base substitution C T intron_variant MELA-AU 11 70254861 70254862 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 70254861 70254862 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 70254881 70254881 single base substitution C T downstream_gene_variant MELA-AU 11 70254881 70254881 single base substitution C T intron_variant MELA-AU 11 70254945 70254945 single base substitution C T downstream_gene_variant MELA-AU 11 70254945 70254945 single base substitution C T intron_variant MELA-AU 11 70255222 70255222 single base substitution C T downstream_gene_variant MELA-AU 11 70255222 70255222 single base substitution C T intron_variant MELA-AU 11 70255386 70255386 single base substitution C T downstream_gene_variant MELA-AU 11 70255386 70255386 single base substitution C T intron_variant MELA-AU 11 70256052 70256052 single base substitution G A downstream_gene_variant MELA-AU 11 70256052 70256052 single base substitution G A exon_variant MELA-AU 11 70256052 70256052 single base substitution G A missense_variant D74N 220G>A MELA-AU 11 70256052 70256052 single base substitution G A missense_variant D93N 277G>A MELA-AU 11 70256052 70256052 single base substitution G A upstream_gene_variant MELA-AU 11 70256299 70256299 single base substitution G T downstream_gene_variant MELA-AU 11 70256299 70256299 single base substitution G T intron_variant MELA-AU 11 70256299 70256299 single base substitution G T upstream_gene_variant MELA-AU 11 70256754 70256754 single base substitution C T downstream_gene_variant MELA-AU 11 70256754 70256754 single base substitution C T intron_variant MELA-AU 11 70256754 70256754 single base substitution C T upstream_gene_variant MELA-AU 11 70257307 70257307 single base substitution C A downstream_gene_variant MELA-AU 11 70257307 70257307 single base substitution C A intron_variant MELA-AU 11 70257307 70257307 single base substitution C A upstream_gene_variant MELA-AU 11 70257513 70257513 single base substitution C T downstream_gene_variant MELA-AU 11 70257513 70257513 single base substitution C T intron_variant MELA-AU 11 70257513 70257513 single base substitution C T upstream_gene_variant MELA-AU 11 70257960 70257960 single base substitution C T downstream_gene_variant MELA-AU 11 70257960 70257960 single base substitution C T intron_variant MELA-AU 11 70257960 70257960 single base substitution C T upstream_gene_variant MELA-AU 11 70258111 70258111 single base substitution C T downstream_gene_variant MELA-AU 11 70258111 70258111 single base substitution C T intron_variant MELA-AU 11 70258111 70258111 single base substitution C T upstream_gene_variant MELA-AU 11 70258147 70258147 single base substitution A C downstream_gene_variant MELA-AU 11 70258147 70258147 single base substitution A C intron_variant MELA-AU 11 70258147 70258147 single base substitution A C upstream_gene_variant MELA-AU 11 70258876 70258876 single base substitution C T downstream_gene_variant MELA-AU 11 70258876 70258876 single base substitution C T intron_variant MELA-AU 11 70258876 70258876 single base substitution C T upstream_gene_variant MELA-AU 11 70258932 70258932 single base substitution C T downstream_gene_variant MELA-AU 11 70258932 70258932 single base substitution C T intron_variant MELA-AU 11 70258932 70258932 single base substitution C T upstream_gene_variant MELA-AU 11 70258955 70258955 single base substitution C T downstream_gene_variant MELA-AU 11 70258955 70258955 single base substitution C T intron_variant MELA-AU 11 70258955 70258955 single base substitution C T upstream_gene_variant MELA-AU 11 70258956 70258956 single base substitution C T downstream_gene_variant MELA-AU 11 70258956 70258956 single base substitution C T intron_variant MELA-AU 11 70258956 70258956 single base substitution C T upstream_gene_variant MELA-AU 11 70259023 70259023 single base substitution C T downstream_gene_variant MELA-AU 11 70259023 70259023 single base substitution C T intron_variant MELA-AU 11 70259023 70259023 single base substitution C T upstream_gene_variant MELA-AU 11 70259263 70259263 single base substitution C T downstream_gene_variant MELA-AU 11 70259263 70259263 single base substitution C T intron_variant MELA-AU 11 70259263 70259263 single base substitution C T upstream_gene_variant MELA-AU 11 70260589 70260589 single base substitution G A downstream_gene_variant MELA-AU 11 70260589 70260589 single base substitution G A intron_variant MELA-AU 11 70260589 70260589 single base substitution G A upstream_gene_variant MELA-AU 11 70261044 70261044 single base substitution C T downstream_gene_variant MELA-AU 11 70261044 70261044 single base substitution C T intron_variant MELA-AU 11 70261044 70261044 single base substitution C T upstream_gene_variant MELA-AU 11 70262123 70262123 single base substitution C T exon_variant MELA-AU 11 70262123 70262123 single base substitution C T intron_variant MELA-AU 11 70262123 70262123 single base substitution C T upstream_gene_variant MELA-AU 11 70262186 70262186 single base substitution C T exon_variant MELA-AU 11 70262186 70262186 single base substitution C T intron_variant MELA-AU 11 70262186 70262186 single base substitution C T upstream_gene_variant MELA-AU 11 70262518 70262518 single base substitution C T downstream_gene_variant MELA-AU 11 70262518 70262518 single base substitution C T intron_variant MELA-AU 11 70262518 70262518 single base substitution C T upstream_gene_variant MELA-AU 11 70263437 70263437 insertion of <=200bp - T downstream_gene_variant MELA-AU 11 70263437 70263437 insertion of <=200bp - T intron_variant MELA-AU 11 70263437 70263437 insertion of <=200bp - T upstream_gene_variant MELA-AU 11 70263455 70263455 single base substitution T C downstream_gene_variant MELA-AU 11 70263455 70263455 single base substitution T C intron_variant MELA-AU 11 70263455 70263455 single base substitution T C upstream_gene_variant MELA-AU 11 70263821 70263821 single base substitution T C downstream_gene_variant MELA-AU 11 70263821 70263821 single base substitution T C intron_variant MELA-AU 11 70263821 70263821 single base substitution T C upstream_gene_variant MELA-AU 11 70263916 70263916 single base substitution G A downstream_gene_variant MELA-AU 11 70263916 70263916 single base substitution G A intron_variant MELA-AU 11 70263916 70263916 single base substitution G A upstream_gene_variant MELA-AU 11 70264614 70264618 deletion of <=200bp TGTTA - downstream_gene_variant MELA-AU 11 70264614 70264618 deletion of <=200bp TGTTA - intron_variant MELA-AU 11 70264614 70264618 deletion of <=200bp TGTTA - upstream_gene_variant MELA-AU 11 70265510 70265510 single base substitution C T downstream_gene_variant MELA-AU 11 70265510 70265510 single base substitution C T intron_variant MELA-AU 11 70265510 70265510 single base substitution C T upstream_gene_variant MELA-AU 11 70266273 70266273 single base substitution C T 3_prime_UTR_variant MELA-AU 11 70266273 70266273 single base substitution C T 5_prime_UTR_variant MELA-AU 11 70266273 70266273 single base substitution C T downstream_gene_variant MELA-AU 11 70266273 70266273 single base substitution C T intron_variant MELA-AU 11 70266273 70266273 single base substitution C T upstream_gene_variant MELA-AU 11 70266355 70266355 single base substitution C T 3_prime_UTR_variant MELA-AU 11 70266355 70266355 single base substitution C T 5_prime_UTR_variant MELA-AU 11 70266355 70266355 single base substitution C T downstream_gene_variant MELA-AU 11 70266355 70266355 single base substitution C T exon_variant MELA-AU 11 70266355 70266355 single base substitution C T intron_variant MELA-AU 11 70266355 70266355 single base substitution C T upstream_gene_variant MELA-AU 11 70267122 70267122 single base substitution C T downstream_gene_variant MELA-AU 11 70267122 70267122 single base substitution C T intron_variant MELA-AU 11 70267122 70267122 single base substitution C T upstream_gene_variant MELA-AU 11 70267630 70267631 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 70267630 70267631 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 11 70267630 70267631 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 70267630 70267631 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant S282F 845CC>TT MELA-AU 11 70267630 70267631 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 70267714 70267714 single base substitution C T downstream_gene_variant MELA-AU 11 70267714 70267714 single base substitution C T exon_variant MELA-AU 11 70267714 70267714 single base substitution C T intron_variant MELA-AU 11 70267714 70267714 single base substitution C T upstream_gene_variant MELA-AU 11 70268375 70268375 single base substitution C T downstream_gene_variant MELA-AU 11 70268375 70268375 single base substitution C T exon_variant MELA-AU 11 70268375 70268375 single base substitution C T intron_variant MELA-AU 11 70268375 70268375 single base substitution C T upstream_gene_variant MELA-AU 11 70268499 70268499 single base substitution C T downstream_gene_variant MELA-AU 11 70268499 70268499 single base substitution C T exon_variant MELA-AU 11 70268499 70268499 single base substitution C T intron_variant MELA-AU 11 70268499 70268499 single base substitution C T upstream_gene_variant MELA-AU 11 70268920 70268920 single base substitution C T downstream_gene_variant MELA-AU 11 70268920 70268920 single base substitution C T exon_variant MELA-AU 11 70268920 70268920 single base substitution C T intron_variant MELA-AU 11 70269117 70269117 single base substitution C T downstream_gene_variant MELA-AU 11 70269117 70269117 single base substitution C T intron_variant MELA-AU 11 70269605 70269605 single base substitution C T downstream_gene_variant MELA-AU 11 70269605 70269605 single base substitution C T intron_variant MELA-AU 11 70269723 70269723 single base substitution T C downstream_gene_variant MELA-AU 11 70269723 70269723 single base substitution T C intron_variant MELA-AU 11 70269745 70269745 single base substitution G A downstream_gene_variant MELA-AU 11 70269745 70269745 single base substitution G A intron_variant MELA-AU 11 70269759 70269759 single base substitution G A downstream_gene_variant MELA-AU 11 70269759 70269759 single base substitution G A intron_variant MELA-AU 11 70270741 70270741 single base substitution C T downstream_gene_variant MELA-AU 11 70270741 70270741 single base substitution C T intron_variant MELA-AU 11 70270741 70270741 single base substitution C T upstream_gene_variant MELA-AU 11 70271295 70271295 single base substitution G A downstream_gene_variant MELA-AU 11 70271295 70271295 single base substitution G A intron_variant MELA-AU 11 70271295 70271295 single base substitution G A upstream_gene_variant MELA-AU 11 70271346 70271346 single base substitution C T downstream_gene_variant MELA-AU 11 70271346 70271346 single base substitution C T intron_variant MELA-AU 11 70271346 70271346 single base substitution C T upstream_gene_variant MELA-AU 11 70272298 70272298 single base substitution G T downstream_gene_variant MELA-AU 11 70272298 70272298 single base substitution G T intron_variant MELA-AU 11 70272298 70272298 single base substitution G T upstream_gene_variant MELA-AU 11 70272510 70272510 single base substitution C T downstream_gene_variant MELA-AU 11 70272510 70272510 single base substitution C T intron_variant MELA-AU 11 70272510 70272510 single base substitution C T upstream_gene_variant MELA-AU 11 70272759 70272768 deletion of <=200bp GCTCACTGCA - downstream_gene_variant MELA-AU 11 70272759 70272768 deletion of <=200bp GCTCACTGCA - intron_variant MELA-AU 11 70272759 70272768 deletion of <=200bp GCTCACTGCA - upstream_gene_variant MELA-AU 11 70273000 70273001 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 70273000 70273001 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 70273000 70273001 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 70273084 70273084 single base substitution C T downstream_gene_variant MELA-AU 11 70273084 70273084 single base substitution C T intron_variant MELA-AU 11 70273084 70273084 single base substitution C T upstream_gene_variant MELA-AU 11 70273155 70273155 single base substitution C T downstream_gene_variant MELA-AU 11 70273155 70273155 single base substitution C T intron_variant MELA-AU 11 70273155 70273155 single base substitution C T upstream_gene_variant MELA-AU 11 70274600 70274600 single base substitution C T downstream_gene_variant MELA-AU 11 70274600 70274600 single base substitution C T intron_variant MELA-AU 11 70274600 70274600 single base substitution C T upstream_gene_variant MELA-AU 11 70274606 70274606 single base substitution T A downstream_gene_variant MELA-AU 11 70274606 70274606 single base substitution T A intron_variant MELA-AU 11 70274606 70274606 single base substitution T A upstream_gene_variant MELA-AU 11 70275038 70275038 single base substitution C T downstream_gene_variant MELA-AU 11 70275038 70275038 single base substitution C T intron_variant MELA-AU 11 70275038 70275038 single base substitution C T upstream_gene_variant MELA-AU 11 70276262 70276263 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 70276262 70276263 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 70276368 70276368 single base substitution C T downstream_gene_variant MELA-AU 11 70276368 70276368 single base substitution C T intron_variant MELA-AU 11 70276951 70276951 single base substitution G T downstream_gene_variant MELA-AU 11 70276951 70276951 single base substitution G T intron_variant MELA-AU 11 70277514 70277514 single base substitution C T downstream_gene_variant MELA-AU 11 70277514 70277514 single base substitution C T intron_variant MELA-AU 11 70277549 70277549 single base substitution G A downstream_gene_variant MELA-AU 11 70277549 70277549 single base substitution G A intron_variant MELA-AU 11 70277781 70277781 single base substitution G A downstream_gene_variant MELA-AU 11 70277781 70277781 single base substitution G A intron_variant MELA-AU 11 70277907 70277907 single base substitution C T downstream_gene_variant MELA-AU 11 70277907 70277907 single base substitution C T intron_variant MELA-AU 11 70277965 70277966 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 70277965 70277966 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 70278068 70278068 single base substitution C A downstream_gene_variant MELA-AU 11 70278068 70278068 single base substitution C A intron_variant MELA-AU 11 70278385 70278385 single base substitution C T downstream_gene_variant MELA-AU 11 70278385 70278385 single base substitution C T intron_variant MELA-AU 11 70279371 70279371 single base substitution C T 3_prime_UTR_variant MELA-AU 11 70279371 70279371 single base substitution C T downstream_gene_variant MELA-AU 11 70279371 70279371 single base substitution C T exon_variant MELA-AU 11 70279371 70279371 single base substitution C T synonymous_variant G134G 402C>T MELA-AU 11 70279371 70279371 single base substitution C T synonymous_variant G161G 483C>T MELA-AU 11 70279371 70279371 single base substitution C T synonymous_variant G440G 1320C>T MELA-AU 11 70279371 70279371 single base substitution C T synonymous_variant G477G 1431C>T MELA-AU 11 70279980 70279980 single base substitution C T downstream_gene_variant MELA-AU 11 70279980 70279980 single base substitution C T intron_variant MELA-AU 11 70280010 70280010 single base substitution C T downstream_gene_variant MELA-AU 11 70280010 70280010 single base substitution C T intron_variant MELA-AU 11 70280134 70280134 single base substitution C T downstream_gene_variant MELA-AU 11 70280134 70280134 single base substitution C T intron_variant MELA-AU 11 70280320 70280320 single base substitution C T intron_variant MELA-AU 11 70280923 70280923 single base substitution T C intron_variant MELA-AU 11 70281625 70281625 single base substitution G T 3_prime_UTR_variant MELA-AU 11 70281625 70281625 single base substitution G T downstream_gene_variant MELA-AU 11 70281625 70281625 single base substitution G T missense_variant C212F 635G>T MELA-AU 11 70281625 70281625 single base substitution G T missense_variant C239F 716G>T MELA-AU 11 70281625 70281625 single base substitution G T missense_variant C518F 1553G>T MELA-AU 11 70281791 70281791 single base substitution G A 3_prime_UTR_variant MELA-AU 11 70281791 70281791 single base substitution G A downstream_gene_variant MELA-AU 11 70281791 70281791 single base substitution G A intron_variant MELA-AU 11 70281791 70281791 single base substitution G A synonymous_variant R294R 882G>A MELA-AU 11 70281791 70281791 single base substitution G A synonymous_variant R573R 1719G>A MELA-AU 11 70282254 70282254 single base substitution C T 3_prime_UTR_variant MELA-AU 11 70282254 70282254 single base substitution C T downstream_gene_variant MELA-AU 11 70282254 70282254 single base substitution C T intron_variant MELA-AU 11 70283153 70283153 single base substitution C T downstream_gene_variant MELA-AU 11 70283496 70283496 single base substitution G A downstream_gene_variant MELA-AU 11 70283864 70283864 single base substitution C T downstream_gene_variant MELA-AU 11 70283872 70283872 single base substitution C T downstream_gene_variant MELA-AU 11 70284058 70284058 single base substitution C T downstream_gene_variant MELA-AU 11 70284316 70284316 single base substitution G A downstream_gene_variant MELA-AU 11 70284575 70284575 single base substitution C T downstream_gene_variant MELA-AU 11 70284959 70284959 single base substitution G A downstream_gene_variant MELA-AU 11 70285116 70285116 single base substitution C T downstream_gene_variant MELA-AU 11 70285212 70285212 single base substitution A G downstream_gene_variant MELA-AU 11 70285259 70285259 single base substitution C T downstream_gene_variant MELA-AU 11 70285277 70285277 single base substitution C T downstream_gene_variant MELA-AU 11 70285374 70285374 single base substitution C T downstream_gene_variant MELA-AU 11 70285753 70285753 single base substitution G A downstream_gene_variant MELA-AU 11 70285977 70285977 single base substitution C T downstream_gene_variant MELA-AU 11 70286204 70286204 single base substitution C T downstream_gene_variant MELA-AU 11 70286457 70286457 single base substitution C T downstream_gene_variant MELA-AU 11 70286704 70286704 single base substitution G A downstream_gene_variant MELA-AU 11 70287101 70287101 single base substitution G A downstream_gene_variant MELA-AU 11 70287323 70287323 single base substitution G A downstream_gene_variant ORCA-IN 11 70248662 70248662 single base substitution C T intron_variant ORCA-IN 11 70248662 70248662 single base substitution C T upstream_gene_variant ORCA-IN 11 70258040 70258040 single base substitution G A downstream_gene_variant ORCA-IN 11 70258040 70258040 single base substitution G A intron_variant ORCA-IN 11 70258040 70258040 single base substitution G A upstream_gene_variant OV-AU 11 70244918 70244918 single base substitution G A intron_variant OV-AU 11 70251338 70251338 single base substitution C T intron_variant OV-AU 11 70251338 70251338 single base substitution C T upstream_gene_variant OV-AU 11 70252885 70252885 single base substitution A G intron_variant OV-AU 11 70252885 70252885 single base substitution A G upstream_gene_variant OV-AU 11 70274503 70274503 single base substitution C T downstream_gene_variant OV-AU 11 70274503 70274503 single base substitution C T intron_variant OV-AU 11 70274503 70274503 single base substitution C T upstream_gene_variant OV-AU 11 70276411 70276411 single base substitution C T downstream_gene_variant OV-AU 11 70276411 70276411 single base substitution C T intron_variant OV-AU 11 70279420 70279420 single base substitution G A downstream_gene_variant OV-AU 11 70279420 70279420 single base substitution G A intron_variant OV-AU 11 70279496 70279496 single base substitution T C downstream_gene_variant OV-AU 11 70279496 70279496 single base substitution T C intron_variant OV-AU 11 70280928 70280928 single base substitution C T intron_variant OV-AU 11 70283622 70283622 single base substitution G C downstream_gene_variant PACA-AU 11 70239865 70239865 single base substitution C T upstream_gene_variant PACA-AU 11 70241239 70241239 single base substitution G A upstream_gene_variant PACA-AU 11 70243133 70243133 single base substitution A T upstream_gene_variant PACA-AU 11 70245031 70245031 single base substitution G T intron_variant PACA-AU 11 70249069 70249069 single base substitution C T intron_variant PACA-AU 11 70249069 70249069 single base substitution C T upstream_gene_variant PACA-AU 11 70254732 70254732 single base substitution C G downstream_gene_variant PACA-AU 11 70254732 70254732 single base substitution C G intron_variant PACA-AU 11 70257060 70257060 single base substitution G A downstream_gene_variant PACA-AU 11 70257060 70257060 single base substitution G A intron_variant PACA-AU 11 70257060 70257060 single base substitution G A upstream_gene_variant PACA-AU 11 70258262 70258262 insertion of <=200bp - G downstream_gene_variant PACA-AU 11 70258262 70258262 insertion of <=200bp - G intron_variant PACA-AU 11 70258262 70258262 insertion of <=200bp - G upstream_gene_variant PACA-AU 11 70258818 70258818 single base substitution C T downstream_gene_variant PACA-AU 11 70258818 70258818 single base substitution C T intron_variant PACA-AU 11 70258818 70258818 single base substitution C T upstream_gene_variant PACA-AU 11 70263792 70263792 single base substitution G T downstream_gene_variant PACA-AU 11 70263792 70263792 single base substitution G T intron_variant PACA-AU 11 70263792 70263792 single base substitution G T upstream_gene_variant PACA-AU 11 70264633 70264633 single base substitution G T downstream_gene_variant PACA-AU 11 70264633 70264633 single base substitution G T intron_variant PACA-AU 11 70264633 70264633 single base substitution G T upstream_gene_variant PACA-AU 11 70267606 70267606 single base substitution G T downstream_gene_variant PACA-AU 11 70267606 70267606 single base substitution G T exon_variant PACA-AU 11 70267606 70267606 single base substitution G T intron_variant PACA-AU 11 70267606 70267606 single base substitution G T missense_variant G274V 821G>T PACA-AU 11 70267606 70267606 single base substitution G T upstream_gene_variant PACA-AU 11 70267616 70267616 single base substitution G A downstream_gene_variant PACA-AU 11 70267616 70267616 single base substitution G A exon_variant PACA-AU 11 70267616 70267616 single base substitution G A intron_variant PACA-AU 11 70267616 70267616 single base substitution G A synonymous_variant S277S 831G>A PACA-AU 11 70267616 70267616 single base substitution G A upstream_gene_variant PACA-AU 11 70269275 70269275 single base substitution G A downstream_gene_variant PACA-AU 11 70269275 70269275 single base substitution G A intron_variant PACA-AU 11 70273502 70273502 single base substitution C T downstream_gene_variant PACA-AU 11 70273502 70273502 single base substitution C T intron_variant PACA-AU 11 70273502 70273502 single base substitution C T upstream_gene_variant PACA-AU 11 70275206 70275206 single base substitution G A 3_prime_UTR_variant PACA-AU 11 70275206 70275206 single base substitution G A downstream_gene_variant PACA-AU 11 70275206 70275206 single base substitution G A synonymous_variant K16K 48G>A PACA-AU 11 70275206 70275206 single base substitution G A synonymous_variant K322K 966G>A PACA-AU 11 70275206 70275206 single base substitution G A synonymous_variant K359K 1077G>A PACA-AU 11 70275206 70275206 single base substitution G A synonymous_variant K43K 129G>A PACA-AU 11 70275206 70275206 single base substitution G A upstream_gene_variant PACA-AU 11 70275212 70275212 single base substitution A G 3_prime_UTR_variant PACA-AU 11 70275212 70275212 single base substitution A G downstream_gene_variant PACA-AU 11 70275212 70275212 single base substitution A G synonymous_variant K18K 54A>G PACA-AU 11 70275212 70275212 single base substitution A G synonymous_variant K324K 972A>G PACA-AU 11 70275212 70275212 single base substitution A G synonymous_variant K361K 1083A>G PACA-AU 11 70275212 70275212 single base substitution A G synonymous_variant K45K 135A>G PACA-AU 11 70275212 70275212 single base substitution A G upstream_gene_variant PACA-AU 11 70275668 70275668 single base substitution C T downstream_gene_variant PACA-AU 11 70275668 70275668 single base substitution C T intron_variant PACA-AU 11 70276060 70276060 single base substitution T C downstream_gene_variant PACA-AU 11 70276060 70276060 single base substitution T C intron_variant PACA-AU 11 70277322 70277322 single base substitution C T 3_prime_UTR_variant PACA-AU 11 70277322 70277322 single base substitution C T downstream_gene_variant PACA-AU 11 70277322 70277322 single base substitution C T exon_variant PACA-AU 11 70277322 70277322 single base substitution C T missense_variant T364M 1091C>T PACA-AU 11 70277322 70277322 single base substitution C T missense_variant T401M 1202C>T PACA-AU 11 70277322 70277322 single base substitution C T missense_variant T58M 173C>T PACA-AU 11 70277322 70277322 single base substitution C T missense_variant T85M 254C>T PACA-AU 11 70278260 70278260 single base substitution C T downstream_gene_variant PACA-AU 11 70278260 70278260 single base substitution C T intron_variant PACA-AU 11 70278436 70278436 deletion of <=200bp G - downstream_gene_variant PACA-AU 11 70278436 70278436 deletion of <=200bp G - intron_variant PACA-AU 11 70281872 70281872 single base substitution G T 3_prime_UTR_variant PACA-AU 11 70281872 70281872 single base substitution G T downstream_gene_variant PACA-AU 11 70281872 70281872 single base substitution G T intron_variant PACA-AU 11 70286074 70286074 single base substitution G T downstream_gene_variant PACA-AU 11 70287152 70287152 single base substitution C T downstream_gene_variant PACA-CA 11 70240137 70240137 single base substitution G C upstream_gene_variant PACA-CA 11 70241736 70241736 single base substitution C T upstream_gene_variant PACA-CA 11 70243133 70243133 single base substitution A T upstream_gene_variant PACA-CA 11 70243245 70243245 single base substitution C T upstream_gene_variant PACA-CA 11 70243519 70243519 single base substitution C T upstream_gene_variant PACA-CA 11 70248857 70248858 deletion of <=200bp TC - intron_variant PACA-CA 11 70248857 70248858 deletion of <=200bp TC - upstream_gene_variant PACA-CA 11 70249114 70249114 single base substitution A T intron_variant PACA-CA 11 70249114 70249114 single base substitution A T upstream_gene_variant PACA-CA 11 70249962 70249962 single base substitution A C intron_variant PACA-CA 11 70249962 70249962 single base substitution A C upstream_gene_variant PACA-CA 11 70249987 70249987 single base substitution T C intron_variant PACA-CA 11 70249987 70249987 single base substitution T C upstream_gene_variant PACA-CA 11 70250864 70250864 single base substitution T G intron_variant PACA-CA 11 70250864 70250864 single base substitution T G upstream_gene_variant PACA-CA 11 70253724 70253724 single base substitution G A exon_variant PACA-CA 11 70253724 70253724 single base substitution G A intron_variant PACA-CA 11 70254493 70254496 deletion of <=200bp ATTT - downstream_gene_variant PACA-CA 11 70254493 70254496 deletion of <=200bp ATTT - intron_variant PACA-CA 11 70255135 70255135 single base substitution A G downstream_gene_variant PACA-CA 11 70255135 70255135 single base substitution A G intron_variant PACA-CA 11 70258681 70258681 single base substitution A G downstream_gene_variant PACA-CA 11 70258681 70258681 single base substitution A G intron_variant PACA-CA 11 70258681 70258681 single base substitution A G upstream_gene_variant PACA-CA 11 70259983 70259983 single base substitution A G downstream_gene_variant PACA-CA 11 70259983 70259983 single base substitution A G intron_variant PACA-CA 11 70259983 70259983 single base substitution A G upstream_gene_variant PACA-CA 11 70261101 70261101 deletion of <=200bp G - downstream_gene_variant PACA-CA 11 70261101 70261101 deletion of <=200bp G - intron_variant PACA-CA 11 70261101 70261101 deletion of <=200bp G - upstream_gene_variant PACA-CA 11 70265452 70265452 single base substitution G A downstream_gene_variant PACA-CA 11 70265452 70265452 single base substitution G A intron_variant PACA-CA 11 70265452 70265452 single base substitution G A upstream_gene_variant PACA-CA 11 70266925 70266925 single base substitution G T downstream_gene_variant PACA-CA 11 70266925 70266925 single base substitution G T intron_variant PACA-CA 11 70266925 70266925 single base substitution G T upstream_gene_variant PACA-CA 11 70267110 70267124 deletion of <=200bp TGGGTGCCCCTTCCC - downstream_gene_variant PACA-CA 11 70267110 70267124 deletion of <=200bp TGGGTGCCCCTTCCC - intron_variant PACA-CA 11 70267110 70267124 deletion of <=200bp TGGGTGCCCCTTCCC - upstream_gene_variant PACA-CA 11 70270465 70270465 single base substitution C T downstream_gene_variant PACA-CA 11 70270465 70270465 single base substitution C T intron_variant PACA-CA 11 70270465 70270465 single base substitution C T upstream_gene_variant PACA-CA 11 70272410 70272410 single base substitution G A downstream_gene_variant PACA-CA 11 70272410 70272410 single base substitution G A intron_variant PACA-CA 11 70272410 70272410 single base substitution G A upstream_gene_variant PACA-CA 11 70277693 70277693 single base substitution G T downstream_gene_variant PACA-CA 11 70277693 70277693 single base substitution G T intron_variant PACA-CA 11 70281100 70281100 single base substitution T G intron_variant PACA-CA 11 70281676 70281676 single base substitution G A 3_prime_UTR_variant PACA-CA 11 70281676 70281676 single base substitution G A downstream_gene_variant PACA-CA 11 70281676 70281676 single base substitution G A intron_variant PACA-CA 11 70281676 70281676 single base substitution G A missense_variant R256Q 767G>A PACA-CA 11 70281676 70281676 single base substitution G A missense_variant R535Q 1604G>A PACA-CA 11 70285553 70285553 single base substitution G A downstream_gene_variant PAEN-IT 11 70243225 70243225 single base substitution C T upstream_gene_variant PAEN-IT 11 70268888 70268888 single base substitution A G downstream_gene_variant PAEN-IT 11 70268888 70268888 single base substitution A G exon_variant PAEN-IT 11 70268888 70268888 single base substitution A G intron_variant PBCA-DE 11 70247413 70247413 deletion of <=200bp A - intron_variant PBCA-DE 11 70251754 70251754 single base substitution C G intron_variant PBCA-DE 11 70251754 70251754 single base substitution C G upstream_gene_variant PBCA-DE 11 70257909 70257919 deletion of <=200bp AGCAGCCTCTG - downstream_gene_variant PBCA-DE 11 70257909 70257919 deletion of <=200bp AGCAGCCTCTG - intron_variant PBCA-DE 11 70257909 70257919 deletion of <=200bp AGCAGCCTCTG - upstream_gene_variant PBCA-DE 11 70261040 70261040 single base substitution G A downstream_gene_variant PBCA-DE 11 70261040 70261040 single base substitution G A intron_variant PBCA-DE 11 70261040 70261040 single base substitution G A upstream_gene_variant PBCA-DE 11 70271900 70271900 single base substitution C T downstream_gene_variant PBCA-DE 11 70271900 70271900 single base substitution C T intron_variant PBCA-DE 11 70271900 70271900 single base substitution C T upstream_gene_variant PBCA-DE 11 70286927 70286927 single base substitution G A downstream_gene_variant PRAD-CA 11 70242349 70242349 single base substitution G A upstream_gene_variant PRAD-CA 11 70245357 70245357 single base substitution G T intron_variant PRAD-CA 11 70268702 70268702 single base substitution C T 5_prime_UTR_variant PRAD-CA 11 70268702 70268702 single base substitution C T downstream_gene_variant PRAD-CA 11 70268702 70268702 single base substitution C T exon_variant PRAD-CA 11 70268702 70268702 single base substitution C T intron_variant PRAD-CA 11 70268702 70268702 single base substitution C T splice_region_variant PRAD-CA 11 70279605 70279605 single base substitution G T downstream_gene_variant PRAD-CA 11 70279605 70279605 single base substitution G T intron_variant PRAD-UK 11 70259542 70259542 single base substitution G C downstream_gene_variant PRAD-UK 11 70259542 70259542 single base substitution G C intron_variant PRAD-UK 11 70259542 70259542 single base substitution G C upstream_gene_variant PRAD-UK 11 70261060 70261060 single base substitution C A downstream_gene_variant PRAD-UK 11 70261060 70261060 single base substitution C A intron_variant PRAD-UK 11 70261060 70261060 single base substitution C A upstream_gene_variant PRAD-UK 11 70265510 70265510 single base substitution C G downstream_gene_variant PRAD-UK 11 70265510 70265510 single base substitution C G intron_variant PRAD-UK 11 70265510 70265510 single base substitution C G upstream_gene_variant PRAD-UK 11 70265904 70265904 single base substitution T C downstream_gene_variant PRAD-UK 11 70265904 70265904 single base substitution T C exon_variant PRAD-UK 11 70265904 70265904 single base substitution T C synonymous_variant D188D 564T>C PRAD-UK 11 70265904 70265904 single base substitution T C synonymous_variant D207D 621T>C PRAD-UK 11 70265904 70265904 single base substitution T C upstream_gene_variant PRAD-UK 11 70271627 70271627 single base substitution C T downstream_gene_variant PRAD-UK 11 70271627 70271627 single base substitution C T intron_variant PRAD-UK 11 70271627 70271627 single base substitution C T upstream_gene_variant PRAD-UK 11 70273406 70273406 single base substitution G A downstream_gene_variant PRAD-UK 11 70273406 70273406 single base substitution G A intron_variant PRAD-UK 11 70273406 70273406 single base substitution G A upstream_gene_variant PRAD-UK 11 70282910 70282910 insertion of <=200bp - T downstream_gene_variant PRAD-UK 11 70286060 70286060 single base substitution G C downstream_gene_variant PRAD-UK 11 70286291 70286291 single base substitution T G downstream_gene_variant PRAD-UK 11 70286854 70286854 single base substitution T A downstream_gene_variant PRAD-UK 11 70286857 70286857 single base substitution T A downstream_gene_variant PRAD-UK 11 70287317 70287317 single base substitution A G downstream_gene_variant PRAD-US 11 70282413 70282413 single base substitution C T 3_prime_UTR_variant PRAD-US 11 70282413 70282413 single base substitution C T downstream_gene_variant PRAD-US 11 70282413 70282413 single base substitution C T missense_variant R233W 697C>T PRAD-US 11 70282413 70282413 single base substitution C T missense_variant R602W 1804C>T READ-US 11 70253451 70253451 single base substitution C T exon_variant READ-US 11 70253451 70253451 single base substitution C T synonymous_variant D16D 48C>T READ-US 11 70253451 70253451 single base substitution C T upstream_gene_variant READ-US 11 70277323 70277323 single base substitution G A 3_prime_UTR_variant READ-US 11 70277323 70277323 single base substitution G A downstream_gene_variant READ-US 11 70277323 70277323 single base substitution G A exon_variant READ-US 11 70277323 70277323 single base substitution G A synonymous_variant T364T 1092G>A READ-US 11 70277323 70277323 single base substitution G A synonymous_variant T401T 1203G>A READ-US 11 70277323 70277323 single base substitution G A synonymous_variant T58T 174G>A READ-US 11 70277323 70277323 single base substitution G A synonymous_variant T85T 255G>A RECA-EU 11 70242840 70242840 single base substitution G A upstream_gene_variant RECA-EU 11 70246408 70246408 single base substitution C T intron_variant RECA-EU 11 70256402 70256402 single base substitution C A downstream_gene_variant RECA-EU 11 70256402 70256402 single base substitution C A intron_variant RECA-EU 11 70256402 70256402 single base substitution C A upstream_gene_variant RECA-EU 11 70256623 70256623 single base substitution A G downstream_gene_variant RECA-EU 11 70256623 70256623 single base substitution A G intron_variant RECA-EU 11 70256623 70256623 single base substitution A G upstream_gene_variant RECA-EU 11 70266238 70266238 single base substitution C T 3_prime_UTR_variant RECA-EU 11 70266238 70266238 single base substitution C T 5_prime_UTR_variant RECA-EU 11 70266238 70266238 single base substitution C T downstream_gene_variant RECA-EU 11 70266238 70266238 single base substitution C T intron_variant RECA-EU 11 70266238 70266238 single base substitution C T upstream_gene_variant RECA-EU 11 70267935 70267935 single base substitution A G downstream_gene_variant RECA-EU 11 70267935 70267935 single base substitution A G exon_variant RECA-EU 11 70267935 70267935 single base substitution A G intron_variant RECA-EU 11 70267935 70267935 single base substitution A G upstream_gene_variant SKCA-BR 11 70243639 70243639 insertion of <=200bp - CG upstream_gene_variant SKCA-BR 11 70243641 70243641 single base substitution A G upstream_gene_variant SKCA-BR 11 70245043 70245043 single base substitution A G intron_variant SKCA-BR 11 70247859 70247859 single base substitution G A intron_variant SKCA-BR 11 70252627 70252627 insertion of <=200bp - GA intron_variant SKCA-BR 11 70252627 70252627 insertion of <=200bp - GA upstream_gene_variant SKCA-BR 11 70253401 70253401 single base substitution C T splice_region_variant SKCA-BR 11 70253401 70253401 single base substitution C T upstream_gene_variant SKCA-BR 11 70253427 70253427 single base substitution C G exon_variant SKCA-BR 11 70253427 70253427 single base substitution C G missense_variant H8Q 24C>G SKCA-BR 11 70253427 70253427 single base substitution C G upstream_gene_variant SKCA-BR 11 70254411 70254411 single base substitution C T exon_variant SKCA-BR 11 70254411 70254411 single base substitution C T intron_variant SKCA-BR 11 70254412 70254412 single base substitution C T exon_variant SKCA-BR 11 70254412 70254412 single base substitution C T intron_variant SKCA-BR 11 70255705 70255705 single base substitution C T downstream_gene_variant SKCA-BR 11 70255705 70255705 single base substitution C T intron_variant SKCA-BR 11 70256385 70256385 single base substitution T C downstream_gene_variant SKCA-BR 11 70256385 70256385 single base substitution T C intron_variant SKCA-BR 11 70256385 70256385 single base substitution T C upstream_gene_variant SKCA-BR 11 70257975 70257975 single base substitution C T downstream_gene_variant SKCA-BR 11 70257975 70257975 single base substitution C T intron_variant SKCA-BR 11 70257975 70257975 single base substitution C T upstream_gene_variant SKCA-BR 11 70258170 70258170 single base substitution A G downstream_gene_variant SKCA-BR 11 70258170 70258170 single base substitution A G intron_variant SKCA-BR 11 70258170 70258170 single base substitution A G upstream_gene_variant SKCA-BR 11 70262872 70262872 single base substitution C T downstream_gene_variant SKCA-BR 11 70262872 70262872 single base substitution C T exon_variant SKCA-BR 11 70262872 70262872 single base substitution C T intron_variant SKCA-BR 11 70262872 70262872 single base substitution C T upstream_gene_variant SKCA-BR 11 70266267 70266267 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 70266267 70266267 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 70266267 70266267 single base substitution G A downstream_gene_variant SKCA-BR 11 70266267 70266267 single base substitution G A intron_variant SKCA-BR 11 70266267 70266267 single base substitution G A upstream_gene_variant SKCA-BR 11 70272678 70272678 single base substitution C T downstream_gene_variant SKCA-BR 11 70272678 70272678 single base substitution C T intron_variant SKCA-BR 11 70272678 70272678 single base substitution C T upstream_gene_variant SKCA-BR 11 70273423 70273423 single base substitution C T downstream_gene_variant SKCA-BR 11 70273423 70273423 single base substitution C T intron_variant SKCA-BR 11 70273423 70273423 single base substitution C T upstream_gene_variant SKCA-BR 11 70278639 70278639 single base substitution C T downstream_gene_variant SKCA-BR 11 70278639 70278639 single base substitution C T intron_variant SKCA-BR 11 70279850 70279850 single base substitution A G downstream_gene_variant SKCA-BR 11 70279850 70279850 single base substitution A G intron_variant SKCA-BR 11 70280144 70280144 single base substitution A C downstream_gene_variant SKCA-BR 11 70280144 70280144 single base substitution A C intron_variant SKCA-BR 11 70280200 70280200 single base substitution C T downstream_gene_variant SKCA-BR 11 70280200 70280200 single base substitution C T intron_variant SKCM-US 11 70260694 70260694 single base substitution C T downstream_gene_variant SKCM-US 11 70260694 70260694 single base substitution C T missense_variant S113L 338C>T SKCM-US 11 70260694 70260694 single base substitution C T missense_variant S94L 281C>T SKCM-US 11 70260694 70260694 single base substitution C T upstream_gene_variant SKCM-US 11 70260710 70260710 single base substitution C T downstream_gene_variant SKCM-US 11 70260710 70260710 single base substitution C T synonymous_variant V118V 354C>T SKCM-US 11 70260710 70260710 single base substitution C T synonymous_variant V99V 297C>T SKCM-US 11 70260710 70260710 single base substitution C T upstream_gene_variant SKCM-US 11 70263215 70263215 single base substitution A T downstream_gene_variant SKCM-US 11 70263215 70263215 single base substitution A T exon_variant SKCM-US 11 70263215 70263215 single base substitution A T missense_variant H166L 497A>T SKCM-US 11 70263215 70263215 single base substitution A T missense_variant H185L 554A>T SKCM-US 11 70263215 70263215 single base substitution A T upstream_gene_variant SKCM-US 11 70265858 70265858 single base substitution C T downstream_gene_variant SKCM-US 11 70265858 70265858 single base substitution C T exon_variant SKCM-US 11 70265858 70265858 single base substitution C T missense_variant S173F 518C>T SKCM-US 11 70265858 70265858 single base substitution C T missense_variant S192F 575C>T SKCM-US 11 70265858 70265858 single base substitution C T upstream_gene_variant SKCM-US 11 70265886 70265886 single base substitution C T downstream_gene_variant SKCM-US 11 70265886 70265886 single base substitution C T exon_variant SKCM-US 11 70265886 70265886 single base substitution C T synonymous_variant I182I 546C>T SKCM-US 11 70265886 70265886 single base substitution C T synonymous_variant I201I 603C>T SKCM-US 11 70265886 70265886 single base substitution C T upstream_gene_variant SKCM-US 11 70267599 70267599 single base substitution A G downstream_gene_variant SKCM-US 11 70267599 70267599 single base substitution A G exon_variant SKCM-US 11 70267599 70267599 single base substitution A G intron_variant SKCM-US 11 70267599 70267599 single base substitution A G missense_variant K272E 814A>G SKCM-US 11 70267599 70267599 single base substitution A G upstream_gene_variant SKCM-US 11 70275168 70275168 single base substitution A G 3_prime_UTR_variant SKCM-US 11 70275168 70275168 single base substitution A G downstream_gene_variant SKCM-US 11 70275168 70275168 single base substitution A G missense_variant T310A 928A>G SKCM-US 11 70275168 70275168 single base substitution A G missense_variant T31A 91A>G SKCM-US 11 70275168 70275168 single base substitution A G missense_variant T347A 1039A>G SKCM-US 11 70275168 70275168 single base substitution A G missense_variant T4A 10A>G SKCM-US 11 70275168 70275168 single base substitution A G upstream_gene_variant SKCM-US 11 70275245 70275245 single base substitution G A 3_prime_UTR_variant SKCM-US 11 70275245 70275245 single base substitution G A downstream_gene_variant SKCM-US 11 70275245 70275245 single base substitution G A exon_variant SKCM-US 11 70275245 70275245 single base substitution G A synonymous_variant E29E 87G>A SKCM-US 11 70275245 70275245 single base substitution G A synonymous_variant E335E 1005G>A SKCM-US 11 70275245 70275245 single base substitution G A synonymous_variant E372E 1116G>A SKCM-US 11 70275245 70275245 single base substitution G A synonymous_variant E56E 168G>A STAD-US 11 70253656 70253656 single base substitution T C exon_variant STAD-US 11 70253656 70253656 single base substitution T C synonymous_variant G21G 63T>C STAD-US 11 70253656 70253656 single base substitution T C synonymous_variant G40G 120T>C STAD-US 11 70261793 70261793 single base substitution G A exon_variant STAD-US 11 70261793 70261793 single base substitution G A missense_variant G124R 370G>A STAD-US 11 70261793 70261793 single base substitution G A missense_variant G143R 427G>A STAD-US 11 70261793 70261793 single base substitution G A upstream_gene_variant STAD-US 11 70265913 70265913 single base substitution C A downstream_gene_variant STAD-US 11 70265913 70265913 single base substitution C A exon_variant STAD-US 11 70265913 70265913 single base substitution C A synonymous_variant A191A 573C>A STAD-US 11 70265913 70265913 single base substitution C A synonymous_variant A210A 630C>A STAD-US 11 70265913 70265913 single base substitution C A upstream_gene_variant STAD-US 11 70265939 70265939 single base substitution C T downstream_gene_variant STAD-US 11 70265939 70265939 single base substitution C T exon_variant STAD-US 11 70265939 70265939 single base substitution C T missense_variant T200M 599C>T STAD-US 11 70265939 70265939 single base substitution C T missense_variant T219M 656C>T STAD-US 11 70265939 70265939 single base substitution C T upstream_gene_variant STAD-US 11 70266592 70266592 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 70266592 70266592 single base substitution T A downstream_gene_variant STAD-US 11 70266592 70266592 single base substitution T A exon_variant STAD-US 11 70266592 70266592 single base substitution T A missense_variant L256M 766T>A STAD-US 11 70266592 70266592 single base substitution T A upstream_gene_variant STAD-US 11 70266595 70266595 single base substitution C T 5_prime_UTR_variant STAD-US 11 70266595 70266595 single base substitution C T downstream_gene_variant STAD-US 11 70266595 70266595 single base substitution C T exon_variant STAD-US 11 70266595 70266595 single base substitution C T stop_gained Q257* 769C>T STAD-US 11 70266595 70266595 single base substitution C T upstream_gene_variant STAD-US 11 70275243 70275244 deletion of <=200bp GA - 3_prime_UTR_variant STAD-US 11 70275243 70275244 deletion of <=200bp GA - downstream_gene_variant STAD-US 11 70275243 70275244 deletion of <=200bp GA - exon_variant STAD-US 11 70275243 70275244 deletion of <=200bp GA - frameshift_variant E29 STAD-US 11 70275243 70275244 deletion of <=200bp GA - frameshift_variant E335 STAD-US 11 70275243 70275244 deletion of <=200bp GA - frameshift_variant E372 STAD-US 11 70275243 70275244 deletion of <=200bp GA - frameshift_variant E56 STAD-US 11 70277339 70277339 single base substitution G A 3_prime_UTR_variant STAD-US 11 70277339 70277339 single base substitution G A downstream_gene_variant STAD-US 11 70277339 70277339 single base substitution G A exon_variant STAD-US 11 70277339 70277339 single base substitution G A missense_variant A370T 1108G>A STAD-US 11 70277339 70277339 single base substitution G A missense_variant A407T 1219G>A STAD-US 11 70277339 70277339 single base substitution G A missense_variant A64T 190G>A STAD-US 11 70277339 70277339 single base substitution G A missense_variant A91T 271G>A STAD-US 11 70279801 70279801 single base substitution T C 3_prime_UTR_variant STAD-US 11 70279801 70279801 single base substitution T C downstream_gene_variant STAD-US 11 70279801 70279801 single base substitution T C missense_variant V155A 464T>C STAD-US 11 70279801 70279801 single base substitution T C missense_variant V182A 545T>C STAD-US 11 70279801 70279801 single base substitution T C missense_variant V461A 1382T>C STAD-US 11 70279801 70279801 single base substitution T C missense_variant V498A 1493T>C THCA-US 11 70282508 70282508 single base substitution C T 3_prime_UTR_variant THCA-US 11 70282508 70282508 single base substitution C T downstream_gene_variant THCA-US 11 70282508 70282508 single base substitution C T synonymous_variant C264C 792C>T THCA-US 11 70282508 70282508 single base substitution C T synonymous_variant C633C 1899C>T UCEC-US 11 70260674 70260674 single base substitution G A downstream_gene_variant UCEC-US 11 70260674 70260674 single base substitution G A synonymous_variant S106S 318G>A UCEC-US 11 70260674 70260674 single base substitution G A synonymous_variant S87S 261G>A UCEC-US 11 70260674 70260674 single base substitution G A upstream_gene_variant UCEC-US 11 70263163 70263163 single base substitution C T downstream_gene_variant UCEC-US 11 70263163 70263163 single base substitution C T exon_variant UCEC-US 11 70263163 70263163 single base substitution C T stop_gained R149* 445C>T UCEC-US 11 70263163 70263163 single base substitution C T stop_gained R168* 502C>T UCEC-US 11 70263163 70263163 single base substitution C T upstream_gene_variant UCEC-US 11 70265910 70265910 single base substitution C T downstream_gene_variant UCEC-US 11 70265910 70265910 single base substitution C T exon_variant UCEC-US 11 70265910 70265910 single base substitution C T synonymous_variant S190S 570C>T UCEC-US 11 70265910 70265910 single base substitution C T synonymous_variant S209S 627C>T UCEC-US 11 70265910 70265910 single base substitution C T upstream_gene_variant UCEC-US 11 70269062 70269062 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 11 70269062 70269062 single base substitution C T downstream_gene_variant UCEC-US 11 70269062 70269062 single base substitution C T exon_variant UCEC-US 11 70269062 70269062 single base substitution C T synonymous_variant F269F 807C>T UCEC-US 11 70269062 70269062 single base substitution C T synonymous_variant F306F 918C>T UCEC-US 11 70275184 70275184 single base substitution C T 3_prime_UTR_variant UCEC-US 11 70275184 70275184 single base substitution C T downstream_gene_variant UCEC-US 11 70275184 70275184 single base substitution C T missense_variant A315V 944C>T UCEC-US 11 70275184 70275184 single base substitution C T missense_variant A352V 1055C>T UCEC-US 11 70275184 70275184 single base substitution C T missense_variant A36V 107C>T UCEC-US 11 70275184 70275184 single base substitution C T missense_variant A9V 26C>T UCEC-US 11 70275184 70275184 single base substitution C T upstream_gene_variant UCEC-US 11 70279211 70279211 single base substitution C T 3_prime_UTR_variant UCEC-US 11 70279211 70279211 single base substitution C T downstream_gene_variant UCEC-US 11 70279211 70279211 single base substitution C T exon_variant UCEC-US 11 70279211 70279211 single base substitution C T missense_variant A108V 323C>T UCEC-US 11 70279211 70279211 single base substitution C T missense_variant A387V 1160C>T UCEC-US 11 70279211 70279211 single base substitution C T missense_variant A424V 1271C>T UCEC-US 11 70279211 70279211 single base substitution C T missense_variant A81V 242C>T UCEC-US 11 70279799 70279799 single base substitution C T 3_prime_UTR_variant UCEC-US 11 70279799 70279799 single base substitution C T downstream_gene_variant UCEC-US 11 70279799 70279799 single base substitution C T synonymous_variant A154A 462C>T UCEC-US 11 70279799 70279799 single base substitution C T synonymous_variant A181A 543C>T UCEC-US 11 70279799 70279799 single base substitution C T synonymous_variant A460A 1380C>T UCEC-US 11 70279799 70279799 single base substitution C T synonymous_variant A497A 1491C>T UCEC-US 11 70281136 70281136 single base substitution C T 3_prime_UTR_variant UCEC-US 11 70281136 70281136 single base substitution C T synonymous_variant G164G 492C>T UCEC-US 11 70281136 70281136 single base substitution C T synonymous_variant G191G 573C>T UCEC-US 11 70281136 70281136 single base substitution C T synonymous_variant G470G 1410C>T UCEC-US 11 70281136 70281136 single base substitution C T synonymous_variant G507G 1521C>T UCEC-US 11 70281162 70281162 single base substitution A T 3_prime_UTR_variant UCEC-US 11 70281162 70281162 single base substitution A T missense_variant D173V 518A>T UCEC-US 11 70281162 70281162 single base substitution A T missense_variant D200V 599A>T UCEC-US 11 70281162 70281162 single base substitution A T missense_variant D479V 1436A>T UCEC-US 11 70281162 70281162 single base substitution A T missense_variant D516V 1547A>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T2197 COSM4675503 c.1473C>T p.N491N Substitution - coding silent 11:70433675-70433675 + B98 COSM1746539 c.1447G>A p.D483N Substitution - Missense 11:70433649-70433649 + PTC-7C COSM4146252 c.705A>G p.K235K Substitution - coding silent 11:70420425-70420425 + CHC892T COSM4961399 c.1401G>A p.E467E Substitution - coding silent 11:70433235-70433235 + LAU165 COSM232114 c.286G>A p.D96N Substitution - Missense 11:70409955-70409955 + 587338 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + CSCC-31-T COSM2043970 c.1427C>T p.P476L Substitution - Missense 11:70433261-70433261 + Pat_26_A COSM5839476 c.1445-2_1445-1delAG p.? Unknown 11:70433645-70433646 + MO_1071 COSM4036300 c.427G>A p.G143R Substitution - Missense 11:70415687-70415687 + 8064632 COSM3383794 c.1077G>A p.K359K Substitution - coding silent 11:70429100-70429100 + 8066440 COSM3769433 c.821G>T p.G274V Substitution - Missense 11:70421500-70421500 + LUAD-NYU195 COSM371013 c.791-1G>A p.? Unknown 11:70421469-70421469 + TCGA-EI-6512-01 COSM1356654 c.48C>T p.D16D Substitution - coding silent 11:70407345-70407345 + TCGA-GV-A3QI-01 COSM1298551 c.1212G>C p.V404V Substitution - coding silent 11:70431226-70431226 + T256 COSM4675506 c.1494C>T p.V498V Substitution - coding silent 11:70433696-70433696 + 8066081 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + T84 COSM2043943 c.819C>T p.F273F Substitution - coding silent 11:70421498-70421498 + Pat_24_A COSM5839471 c.503G>A p.R168Q Substitution - Missense 11:70417058-70417058 + TCGA-D9-A1JW-06 COSM3452734 c.1116G>A p.E372E Substitution - coding silent 11:70429139-70429139 + TCGA-ER-A19K-01 COSM3452725 c.575C>T p.S192F Substitution - Missense 11:70419752-70419752 + TCGA-AX-A0J1-01 COSM1585973 c.627C>T p.S209S Substitution - coding silent 11:70419804-70419804 + PDA_094 COSM5003192 c.1180C>A p.Q394K Substitution - Missense 11:70431194-70431194 + HCC19T COSM3703667 c.400C>A p.Q134K Substitution - Missense 11:70414650-70414650 + 587300 COSM1202650 c.1072G>A p.A358T Substitution - Missense 11:70429095-70429095 + PD4120a COSM160270 c.1234G>A p.E412K Substitution - Missense 11:70431248-70431248 + TCGA-AX-A06H-01 COSM931486 c.1521C>T p.G507G Substitution - coding silent 11:70435030-70435030 + PD5964a COSM5778612 c.569-1G>C p.? Unknown 11:70419745-70419745 + TCGA-G4-6586-01 COSM1356675 c.1593C>T p.R531R Substitution - coding silent 11:70435102-70435102 + HT55 COSM2043941 c.750G>T p.W250C Substitution - Missense 11:70420470-70420470 + PT38 COSM5922879 c.292-4C>T p.? Unknown 11:70414538-70414538 + TCGA-FV-A23B-01 COSM4914015 c.367G>A p.G123S Substitution - Missense 11:70414617-70414617 + TCGA-F4-6856-01 COSM1356672 c.1203G>A p.T401T Substitution - coding silent 11:70431217-70431217 + B98-Tumor COSM1746540 c.1447G>A p.D483N Substitution - Missense 11:70433649-70433649 + ESCC_109 COSM5638846 c.675G>A p.Q225Q Substitution - coding silent 11:70419852-70419852 + HCC19T COSM3703668 c.400C>A p.Q134K Substitution - Missense 11:70414650-70414650 + LP6007404-DNA_A01 COSM4416420 c.1126C>T p.R376W Substitution - Missense 11:70429149-70429149 + TCGA-CM-4746-01 COSM1356664 c.546G>A p.T182T Substitution - coding silent 11:70417101-70417101 + 578 COSM3721376 c.485A>G p.Y162C Substitution - Missense 11:70417040-70417040 + HCC19T COSM3703664 c.399T>A p.D133E Substitution - Missense 11:70414649-70414649 + TCGA-CG-4305-01 COSM4036315 c.1219G>A p.A407T Substitution - Missense 11:70431233-70431233 + HCC19 COSM3703668 c.400C>A p.Q134K Substitution - Missense 11:70414650-70414650 + TCGA-BR-8589-01 COSM4036318 c.1493T>C p.V498A Substitution - Missense 11:70433695-70433695 + TCGA-OL-A5DA-01 COSM3810310 c.1484T>G p.I495S Substitution - Missense 11:70433686-70433686 + TCGA-AP-A056-01 COSM931485 c.1271C>T p.A424V Substitution - Missense 11:70433105-70433105 + MO_1013 COSM5553124 c.68A>T p.E23V Substitution - Missense 11:70407365-70407365 + TCGA-HU-A4H4-01 COSM4036297 c.120T>C p.G40G Substitution - coding silent 11:70407550-70407550 + LUAD-B01811 COSM333836 c.53G>T p.G18V Substitution - Missense 11:70407350-70407350 + TCGA-66-2780-01 COSM690153 c.701G>A p.G234E Substitution - Missense 11:70420421-70420421 + 585223 COSM319739 c.163A>T p.I55L Substitution - Missense 11:70409832-70409832 + PR-03-870 COSM243911 c.1387G>A p.A463T Substitution - Missense 11:70433221-70433221 + 8064632 COSM3383795 c.1077G>A p.K359K Substitution - coding silent 11:70429100-70429100 + BD173T COSM5500509 c.321A>G p.K107K Substitution - coding silent 11:70414571-70414571 + CRC-06T COSM1192196 c.245A>G p.H82R Substitution - Missense 11:70409914-70409914 + AA1924 COSM4169006 c.517G>T p.A173S Substitution - Missense 11:70417072-70417072 + RK280_C01 COSM4944395 c.1517-5C>A p.? Unknown 11:70435021-70435021 + 6_tFL COSM4170352 c.1318A>C p.T440P Substitution - Missense 11:70433152-70433152 + T2197 COSM4675502 c.1473C>T p.N491N Substitution - coding silent 11:70433675-70433675 + ccRCC-61 COSM1661329 c.1309G>C p.V437L Substitution - Missense 11:70433143-70433143 + pfg043T COSM4757029 c.982A>G p.T328A Substitution - Missense 11:70425356-70425356 + CSCC-31-T COSM2043971 c.1427C>T p.P476L Substitution - Missense 11:70433261-70433261 + HCC19T COSM3703665 c.399T>A p.D133E Substitution - Missense 11:70414649-70414649 + RKO COSM2043986 c.1518G>A p.A506A Substitution - coding silent 11:70435027-70435027 + TCGA-AP-A059-01 COSM1585965 c.1547A>T p.D516V Substitution - Missense 11:70435056-70435056 + TCGA-22-4604-01 COSM690149 c.1582G>C p.G528R Substitution - Missense 11:70435091-70435091 + TCGA-HU-A4H4-01 COSM4036296 c.120T>C p.G40G Substitution - coding silent 11:70407550-70407550 + B83 COSM1746537 c.958-1G>A p.? Unknown 11:70425331-70425331 + TCGA-BR-4361-01 COSM4036306 c.656C>T p.T219M Substitution - Missense 11:70419833-70419833 + TCGA-66-2744-01 COSM1146776 c.210G>T p.K70N Substitution - Missense 11:70409879-70409879 + PTC-7C COSM4146251 c.705A>G p.K235K Substitution - coding silent 11:70420425-70420425 + C086 COSM5529398 c.186C>T p.V62V Substitution - coding silent 11:70409855-70409855 + B98-Tumor COSM1746539 c.1447G>A p.D483N Substitution - Missense 11:70433649-70433649 + TCGA-ER-A19K-01 COSM3452726 c.575C>T p.S192F Substitution - Missense 11:70419752-70419752 + NPC9D COSM4995044 c.1533C>G p.I511M Substitution - Missense 11:70435042-70435042 + MO_1013 COSM5553123 c.68A>T p.E23V Substitution - Missense 11:70407365-70407365 + TCGA-BG-A18B-01 COSM931481 c.502C>T p.R168* Substitution - Nonsense 11:70417057-70417057 + TCGA-EA-A1QT-01 COSM458410 c.1459G>A p.D487N Substitution - Missense 11:70433661-70433661 + 251 COSM1741892 c.88-8C>G p.? Unknown 11:70407510-70407510 + PT49 COSM5935707 c.140C>T p.S47F Substitution - Missense 11:70407570-70407570 + RK197_C01 COSM2043929 c.499G>A p.D167N Substitution - Missense 11:70417054-70417054 + LC_C8 COSM1188340 c.1232C>T p.T411I Substitution - Missense 11:70431246-70431246 + PD23574a COSM5793676 c.848C>T p.A283V Substitution - Missense 11:70421527-70421527 + HCC009T COSM5819852 c.69G>A p.E23E Substitution - coding silent 11:70407366-70407366 + LIM2405 COSM1585967 c.1271C>T p.A424V Substitution - Missense 11:70433105-70433105 + TCGA-FV-A23B-01 COSM4914016 c.367G>A p.G123S Substitution - Missense 11:70414617-70414617 + TCGA-D5-6930-01 COSM1356654 c.48C>T p.D16D Substitution - coding silent 11:70407345-70407345 + TCGA-CG-5721-01 COSM4036303 c.630C>A p.A210A Substitution - coding silent 11:70419807-70419807 + TCGA-BS-A0U8-01 COSM1152395 c.1491C>T p.A497A Substitution - coding silent 11:70433693-70433693 + TCGA-FW-A3R5-06 COSM2043913 c.338C>T p.S113L Substitution - Missense 11:70414588-70414588 + TCGA-DD-A4NK-01 COSM4935208 c.919G>A p.G307S Substitution - Missense 11:70422957-70422957 + sysucc-880T COSM5462082 c.402+2T>C p.? Unknown 11:70414654-70414654 + T3503 COSM4675496 c.1325C>T p.P442L Substitution - Missense 11:70433159-70433159 + TCGA-06-5410-01 COSM3398106 c.1326G>A p.P442P Substitution - coding silent 11:70433160-70433160 + 251 COSM1741891 c.88-8C>G p.? Unknown 11:70407510-70407510 + pfg043T COSM4757030 c.982A>G p.T328A Substitution - Missense 11:70425356-70425356 + YUPAT COSM1704326 c.590G>A p.G197D Substitution - Missense 11:70419767-70419767 + TCGA-26-6174-01 COSM3398104 c.712G>A p.V238M Substitution - Missense 11:70420432-70420432 + T256 COSM4675505 c.1494C>T p.V498V Substitution - coding silent 11:70433696-70433696 + PT38 COSM5922880 c.292-4C>T p.? Unknown 11:70414538-70414538 + TCGA-GV-A3QI-01 COSM1298550 c.1212G>C p.V404V Substitution - coding silent 11:70431226-70431226 + TCGA-E1-5322-01 COSM3967810 c.437A>G p.E146G Substitution - Missense 11:70415697-70415697 + C086 COSM5529397 c.186C>T p.V62V Substitution - coding silent 11:70409855-70409855 + YUFIT COSM5373469 c.1277C>T p.S426F Substitution - Missense 11:70433111-70433111 + BD173T COSM5500508 c.321A>G p.K107K Substitution - coding silent 11:70414571-70414571 + Pat_06_B COSM5839474 c.970T>C p.F324L Substitution - Missense 11:70425344-70425344 + CSCC-47-T COSM1356670 c.932G>A p.G311E Substitution - Missense 11:70422970-70422970 + CSCC-31-T COSM4508648 c.782C>T p.S261F Substitution - Missense 11:70420502-70420502 + HCC19 COSM3703664 c.399T>A p.D133E Substitution - Missense 11:70414649-70414649 + PT50 COSM5937476 c.679+8C>T p.? Unknown 11:70419864-70419864 + TCGA-EK-A2RJ-01 COSM4831759 c.1052G>C p.R351T Substitution - Missense 11:70429075-70429075 + HT55 COSM2043940 c.750G>T p.W250C Substitution - Missense 11:70420470-70420470 + TCGA-GV-A3JZ-01 COSM1298553 c.1528G>A p.E510K Substitution - Missense 11:70435037-70435037 + NPC9D COSM4995040 c.1485C>G p.I495M Substitution - Missense 11:70433687-70433687 + TCGA-CK-4950-01 COSM1356658 c.359G>T p.G120V Substitution - Missense 11:70414609-70414609 + HCC25 COSM1605162 c.712G>T p.V238L Substitution - Missense 11:70420432-70420432 + PD5964a COSM5778611 c.569-1G>C p.? Unknown 11:70419745-70419745 + RK051_C01 COSM1628197 c.518C>T p.A173V Substitution - Missense 11:70417073-70417073 + YUBER COSM1704323 c.242C>T p.S81F Substitution - Missense 11:70409911-70409911 + ESCC_161 COSM5647542 c.1560C>G p.T520T Substitution - coding silent 11:70435069-70435069 + TCGA-51-4081-01 COSM1146778 c.311A>G p.Y104C Substitution - Missense 11:70414561-70414561 + TCGA-D9-A4Z2-01 COSM3452731 c.1039A>G p.T347A Substitution - Missense 11:70429062-70429062 + TCGA-C4-A0F1-01 COSM415756 c.1614C>T p.Y538Y Substitution - coding silent 11:70435123-70435123 + TCGA-51-4081-01 COSM690154 c.311A>G p.Y104C Substitution - Missense 11:70414561-70414561 + CSCC-20-T COSM4518386 c.629_630CC>TT p.A210V Substitution - Missense 11:70419806-70419807 + TCGA-BT-A3PH-01 COSM1298548 c.646C>G p.Q216E Substitution - Missense 11:70419823-70419823 + TCGA-BR-8081-01 COSM4036311 c.769C>T p.Q257* Substitution - Nonsense 11:70420489-70420489 + TCGA-AG-A002-01 COSM260328 c.585C>T p.F195F Substitution - coding silent 11:70419762-70419762 + PR-09-5702 COSM243909 c.1313G>A p.S438N Substitution - Missense 11:70433147-70433147 + TCGA-CK-4950-01 COSM1356657 c.359G>T p.G120V Substitution - Missense 11:70414609-70414609 + TCGA-AZ-4315-01 COSM1356661 c.397G>T p.D133Y Substitution - Missense 11:70414647-70414647 + TCGA-13-1512-01 COSM70338 c.932G>C p.G311A Substitution - Missense 11:70422970-70422970 + DLBCL-PatientD COSM220322 c.989T>A p.V330E Substitution - Missense 11:70425363-70425363 + 8066067 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + T407 COSM4675499 c.1377G>A p.Q459Q Substitution - coding silent 11:70433211-70433211 + 2217539 COSM4421527 c.1139A>G p.E380G Substitution - Missense 11:70429162-70429162 + Pat_06_B COSM5839473 c.970T>C p.F324L Substitution - Missense 11:70425344-70425344 + TCGA-CG-5721-01 COSM4036302 c.630C>A p.A210A Substitution - coding silent 11:70419807-70419807 + 578 COSM3721375 c.485A>G p.Y162C Substitution - Missense 11:70417040-70417040 + TCGA-BR-7707-01 COSM4036300 c.427G>A p.G143R Substitution - Missense 11:70415687-70415687 + CLL123 COSM1289630 c.948G>A p.R316R Substitution - coding silent 11:70422986-70422986 + S00837 COSM310411 c.1616G>T p.G539V Substitution - Missense 11:70435125-70435125 + ICGC_0034 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + LP6007422-DNA_A01 COSM5034389 c.1438C>G p.P480A Substitution - Missense 11:70433272-70433272 + TCGA-FW-A3R5-06 COSM3870085 c.354C>T p.V118V Substitution - coding silent 11:70414604-70414604 + LUAD-D01603 COSM337293 c.1491C>T p.A497A Substitution - coding silent 11:70433693-70433693 + PC-9BRc1 COSM1685056 c.754C>T p.H252Y Substitution - Missense 11:70420474-70420474 + 587338 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + YUFIT COSM5373470 c.1277C>T p.S426F Substitution - Missense 11:70433111-70433111 + BD6T COSM5499109 c.631G>A p.V211I Substitution - Missense 11:70419808-70419808 + PT48 COSM5932741 c.671C>T p.S224F Substitution - Missense 11:70419848-70419848 + LIM2405 COSM931485 c.1271C>T p.A424V Substitution - Missense 11:70433105-70433105 + T407 COSM4675500 c.1377G>A p.Q459Q Substitution - coding silent 11:70433211-70433211 + YUBER COSM1704324 c.242C>T p.S81F Substitution - Missense 11:70409911-70409911 + TCGA-AP-A056-01 COSM1585967 c.1271C>T p.A424V Substitution - Missense 11:70433105-70433105 + TCGA-AX-A06H-01 COSM1152397 c.1521C>T p.G507G Substitution - coding silent 11:70435030-70435030 + TCGA-RP-A693-06 COSM4895408 c.554A>T p.H185L Substitution - Missense 11:70417109-70417109 + LIM1215 COSM4639352 c.49G>A p.A17T Substitution - Missense 11:70407346-70407346 + 8057513 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + TCGA-CM-4746-01 COSM1356663 c.546G>A p.T182T Substitution - coding silent 11:70417101-70417101 + LP6007422-DNA_A01 COSM5034390 c.1438C>G p.P480A Substitution - Missense 11:70433272-70433272 + LUAD-NYU195 COSM371014 c.809G>A p.G270E Substitution - Missense 11:70421488-70421488 + 2492729 COSM5729793 c.568G>A p.D190N Substitution - Missense 11:70417123-70417123 + CLL123 COSM1289629 c.948G>A p.R316R Substitution - coding silent 11:70422986-70422986 + ESCC_161 COSM5647543 c.1560C>G p.T520T Substitution - coding silent 11:70435069-70435069 + 587300 COSM1202649 c.1072G>A p.A358T Substitution - Missense 11:70429095-70429095 + AA1924 COSM4169007 c.517G>T p.A173S Substitution - Missense 11:70417072-70417072 + T84 COSM2043942 c.819C>T p.F273F Substitution - coding silent 11:70421498-70421498 + TCGA-EI-6507-01 COSM1356672 c.1203G>A p.T401T Substitution - coding silent 11:70431217-70431217 + ACINAR28 COSM1735238 c.967A>G p.T323A Substitution - Missense 11:70425341-70425341 + PT49 COSM5935706 c.140C>T p.S47F Substitution - Missense 11:70407570-70407570 + 8057501 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + PDA_094 COSM5003191 c.1180C>A p.Q394K Substitution - Missense 11:70431194-70431194 + RKO COSM2043987 c.1518G>A p.A506A Substitution - coding silent 11:70435027-70435027 + B83 COSM1746536 c.958-1G>A p.? Unknown 11:70425331-70425331 + HCC19 COSM3703667 c.400C>A p.Q134K Substitution - Missense 11:70414650-70414650 + CSCC-20-T COSM4518387 c.629_630CC>TT p.A210V Substitution - Missense 11:70419806-70419807 + YUPAT COSM1704327 c.590G>A p.G197D Substitution - Missense 11:70419767-70419767 + SJBALL020704_D1 COSM4993833 c.1323G>A p.E441E Substitution - coding silent 11:70433157-70433157 + TCGA-EE-A20F-06 COSM3452729 c.603C>T p.I201I Substitution - coding silent 11:70419780-70419780 + 8066081 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + B9-Tumor COSM3931422 c.698G>A p.G233E Substitution - Missense 11:70420418-70420418 + TCGA-22-4604-01 COSM1146788 c.1582G>C p.G528R Substitution - Missense 11:70435091-70435091 + C086 COSM5529394 c.313C>T p.Q105* Substitution - Nonsense 11:70414563-70414563 + TCGA-G4-6586-01 COSM1356676 c.1593C>T p.R531R Substitution - coding silent 11:70435102-70435102 + TCGA-18-3412-01 COSM1146784 c.1250C>A p.S417* Substitution - Nonsense 11:70431264-70431264 + B9-Tumor COSM3931421 c.698G>A p.G233E Substitution - Missense 11:70420418-70420418 + C086 COSM5529395 c.313C>T p.Q105* Substitution - Nonsense 11:70414563-70414563 + 8047810 COSM3383792 c.831G>A p.S277S Substitution - coding silent 11:70421510-70421510 + sysucc-880T COSM5462081 c.402+2T>C p.? Unknown 11:70414654-70414654 + TCGA-HU-A4H8-01 COSM4036308 c.766T>A p.L256M Substitution - Missense 11:70420486-70420486 + TCGA-HU-A4H8-01 COSM4036309 c.766T>A p.L256M Substitution - Missense 11:70420486-70420486 + TCGA-OL-A5DA-01 COSM3810311 c.1484T>G p.I495S Substitution - Missense 11:70433686-70433686 + H650 COSM1194369 c.1597G>T p.V533L Substitution - Missense 11:70435106-70435106 + TCGA-DD-A4NK-01 COSM4935209 c.919G>A p.G307S Substitution - Missense 11:70422957-70422957 + TCGA-66-2780-01 COSM1146781 c.701G>A p.G234E Substitution - Missense 11:70420421-70420421 + ESCC_109 COSM5638845 c.675G>A p.Q225Q Substitution - coding silent 11:70419852-70419852 + TCGA-B5-A11E-01 COSM931483 c.918C>T p.F306F Substitution - coding silent 11:70422956-70422956 + 3N01-VS-3T01 COSM4978251 c.1492G>A p.V498I Substitution - Missense 11:70433694-70433694 + 2217539 COSM4421528 c.1139A>G p.E380G Substitution - Missense 11:70429162-70429162 + 8047810 COSM3383791 c.831G>A p.S277S Substitution - coding silent 11:70421510-70421510 + 3N01-VS-3T01 COSM4978252 c.1492G>A p.V498I Substitution - Missense 11:70433694-70433694 + LIM1215 COSM4639353 c.49G>A p.A17T Substitution - Missense 11:70407346-70407346 + TCGA-F4-6856-01 COSM1356673 c.1203G>A p.T401T Substitution - coding silent 11:70431217-70431217 + NPC9D COSM4995043 c.1533C>G p.I511M Substitution - Missense 11:70435042-70435042 + TCGA-EE-A20F-06 COSM3452728 c.603C>T p.I201I Substitution - coding silent 11:70419780-70419780 + Pat_24_A COSM5839470 c.503G>A p.R168Q Substitution - Missense 11:70417058-70417058 + TCGA-FW-A3R5-06 COSM3870086 c.354C>T p.V118V Substitution - coding silent 11:70414604-70414604 + ESOSCC155T COSM1171836 c.646C>T p.Q216* Substitution - Nonsense 11:70419823-70419823 + TCGA-FW-A3R5-06 COSM2043914 c.338C>T p.S113L Substitution - Missense 11:70414588-70414588 + HCC25 COSM1605161 c.712G>T p.V238L Substitution - Missense 11:70420432-70420432 + PD23574a COSM5793677 c.848C>T p.A283V Substitution - Missense 11:70421527-70421527 + TCGA-EE-A3J7-06 COSM3870088 c.814A>G p.K272E Substitution - Missense 11:70421493-70421493 + TCGA-EI-6512-01 COSM1356655 c.48C>T p.D16D Substitution - coding silent 11:70407345-70407345 + TCGA-66-2744-01 COSM690155 c.210G>T p.K70N Substitution - Missense 11:70409879-70409879 + CSCC-31-T COSM4515915 c.1425_1426CC>TT p.P476S Substitution - Missense 11:70433259-70433260 + PT50 COSM5937475 c.679+8C>T p.? Unknown 11:70419864-70419864 + 259_T COSM3953756 c.1474G>C p.D492H Substitution - Missense 11:70433676-70433676 + CHC892T COSM4961400 c.1401G>A p.E467E Substitution - coding silent 11:70433235-70433235 + TCGA-AX-A0J1-01 COSM931482 c.627C>T p.S209S Substitution - coding silent 11:70419804-70419804 + LP6007404-DNA_A01 COSM4416419 c.1126C>T p.R376W Substitution - Missense 11:70429149-70429149 + TCGA-A8-A07B-01 COSM429771 c.254G>C p.G85A Substitution - Missense 11:70409923-70409923 + LUAD-CHTN-MAD06-00668 COSM358571 c.999C>G p.A333A Substitution - coding silent 11:70425373-70425373 + 8057513 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + TCGA-BR-8589-01 COSM4036317 c.1493T>C p.V498A Substitution - Missense 11:70433695-70433695 + TCGA-RP-A693-06 COSM4895407 c.554A>T p.H185L Substitution - Missense 11:70417109-70417109 + 8066067 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + B98 COSM1746540 c.1447G>A p.D483N Substitution - Missense 11:70433649-70433649 + ccRCC-61 COSM1661328 c.1309G>C p.V437L Substitution - Missense 11:70433143-70433143 + PC-9BRc1 COSM1685057 c.754C>T p.H252Y Substitution - Missense 11:70420474-70420474 + CRC-06T COSM1192195 c.245A>G p.H82R Substitution - Missense 11:70409914-70409914 + TCGA-B5-A11E-01 COSM1585971 c.918C>T p.F306F Substitution - coding silent 11:70422956-70422956 + TCGA-A5-A0GI-01 COSM1585969 c.1055C>T p.A352V Substitution - Missense 11:70429078-70429078 + 2492729 COSM5729792 c.568G>A p.D190N Substitution - Missense 11:70417123-70417123 + RK051_C01 COSM1628198 c.518C>T p.A173V Substitution - Missense 11:70417073-70417073 + 8058336 COSM3383798 c.1083A>G p.K361K Substitution - coding silent 11:70429106-70429106 + ACINAR28 COSM1735239 c.967A>G p.T323A Substitution - Missense 11:70425341-70425341 + 8058336 COSM3383797 c.1083A>G p.K361K Substitution - coding silent 11:70429106-70429106 + TCGA-E1-5322-01 COSM3967809 c.437A>G p.E146G Substitution - Missense 11:70415697-70415697 + TCGA-BS-A0UV-01 COSM1585975 c.318G>A p.S106S Substitution - coding silent 11:70414568-70414568 + Pat_26_A COSM5839477 c.1445-2_1445-1delAG p.? Unknown 11:70433645-70433646 + 259_T COSM3953755 c.1474G>C p.D492H Substitution - Missense 11:70433676-70433676 + TCGA-BR-7707-01 COSM4036299 c.427G>A p.G143R Substitution - Missense 11:70415687-70415687 + TCGA-GV-A3JZ-01 COSM1298554 c.1528G>A p.E510K Substitution - Missense 11:70435037-70435037 + 8066440 COSM3769432 c.821G>T p.G274V Substitution - Missense 11:70421500-70421500 + BD54T COSM5501927 c.687G>C p.V229V Substitution - coding silent 11:70420407-70420407 + MO_1071 COSM4036299 c.427G>A p.G143R Substitution - Missense 11:70415687-70415687 + TCGA-BR-4361-01 COSM4036305 c.656C>T p.T219M Substitution - Missense 11:70419833-70419833 + 8057501 COSM1158986 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + NPC9D COSM4995041 c.1485C>G p.I495M Substitution - Missense 11:70433687-70433687 + TCGA-06-5410-01 COSM3398107 c.1326G>A p.P442P Substitution - coding silent 11:70433160-70433160 + H650 COSM1194368 c.1597G>T p.V533L Substitution - Missense 11:70435106-70435106 + ESOSCC155T COSM1171835 c.646C>T p.Q216* Substitution - Nonsense 11:70419823-70419823 + CSCC-31-T COSM4452200 c.165A>T p.I55I Substitution - coding silent 11:70409834-70409834 + T3503 COSM4675497 c.1325C>T p.P442L Substitution - Missense 11:70433159-70433159 + BD6T COSM5499110 c.631G>A p.V211I Substitution - Missense 11:70419808-70419808 + TCGA-BR-8081-01 COSM4036312 c.769C>T p.Q257* Substitution - Nonsense 11:70420489-70420489 + TCGA-BS-A0UV-01 COSM931480 c.318G>A p.S106S Substitution - coding silent 11:70414568-70414568 + HCC19 COSM3703665 c.399T>A p.D133E Substitution - Missense 11:70414649-70414649 + 8014753 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + CHC892T COSM4961400 c.1401G>A p.E467E Substitution - coding silent 11:70433235-70433235 + TCGA-EI-6507-01 COSM1356673 c.1203G>A p.T401T Substitution - coding silent 11:70431217-70431217 + TCGA-BG-A18B-01 COSM1152393 c.502C>T p.R168* Substitution - Nonsense 11:70417057-70417057 + 6_tFL COSM4170351 c.1318A>C p.T440P Substitution - Missense 11:70433152-70433152 + TCGA-AZ-4315-01 COSM1356660 c.397G>T p.D133Y Substitution - Missense 11:70414647-70414647 + CHC892T COSM4961399 c.1401G>A p.E467E Substitution - coding silent 11:70433235-70433235 + LC_C8 COSM1188341 c.1232C>T p.T411I Substitution - Missense 11:70431246-70431246 + TCGA-EK-A2RJ-01 COSM4831760 c.1052G>C p.R351T Substitution - Missense 11:70429075-70429075 + TCGA-CG-4305-01 COSM4036314 c.1219G>A p.A407T Substitution - Missense 11:70431233-70431233 + TCGA-AM-5821-01 COSM3752707 c.72C>T p.T24T Substitution - coding silent 11:70407369-70407369 + CSCC-31-T COSM4508647 c.782C>T p.S261F Substitution - Missense 11:70420502-70420502 + TCGA-A5-A0GI-01 COSM931484 c.1055C>T p.A352V Substitution - Missense 11:70429078-70429078 + PT48 COSM5932742 c.671C>T p.S224F Substitution - Missense 11:70419848-70419848 + TCGA-BS-A0U8-01 COSM337293 c.1491C>T p.A497A Substitution - coding silent 11:70433693-70433693 + TCGA-EE-A3J7-06 COSM3870087 c.814A>G p.K272E Substitution - Missense 11:70421493-70421493 + TCGA-D9-A1JW-06 COSM3452735 c.1116G>A p.E372E Substitution - coding silent 11:70429139-70429139 + TCGA-06-5411-01 COSM3398101 c.211G>A p.E71K Substitution - Missense 11:70409880-70409880 + TCGA-18-3412-01 COSM690151 c.1250C>A p.S417* Substitution - Nonsense 11:70431264-70431264 + BD54T COSM5501928 c.687G>C p.V229V Substitution - coding silent 11:70420407-70420407 + B83-Tumor COSM1746536 c.958-1G>A p.? Unknown 11:70425331-70425331 + P06-3939 COSM243910 c.637T>G p.F213V Substitution - Missense 11:70419814-70419814 + TCGA-BT-A3PH-01 COSM1298547 c.646C>G p.Q216E Substitution - Missense 11:70419823-70419823 + HCC009T COSM5819851 c.69G>A p.E23E Substitution - coding silent 11:70407366-70407366 + TCGA-AP-A059-01 COSM931487 c.1547A>T p.D516V Substitution - Missense 11:70435056-70435056 + CSCC-31-T COSM4515916 c.1425_1426CC>TT p.P476S Substitution - Missense 11:70433259-70433260 + HCC25T COSM1605161 c.712G>T p.V238L Substitution - Missense 11:70420432-70420432 + CSCC-31-T COSM4452201 c.165A>T p.I55I Substitution - coding silent 11:70409834-70409834 + TCGA-AM-5821-01 COSM3752706 c.72C>T p.T24T Substitution - coding silent 11:70407369-70407369 + SJBALL020704_D1 COSM4993834 c.1323G>A p.E441E Substitution - coding silent 11:70433157-70433157 + TCGA-A8-A07B-01 COSM1475855 c.254G>C p.G85A Substitution - Missense 11:70409923-70409923 + PD4098a COSM160269 c.1480G>C p.G494R Substitution - Missense 11:70433682-70433682 + TCGA-D9-A4Z2-01 COSM3452732 c.1039A>G p.T347A Substitution - Missense 11:70429062-70429062 + RK197_C01 COSM2043928 c.499G>A p.D167N Substitution - Missense 11:70417054-70417054 + TCGA-D5-6930-01 COSM1356655 c.48C>T p.D16D Substitution - coding silent 11:70407345-70407345 + HCC25T COSM1605162 c.712G>T p.V238L Substitution - Missense 11:70420432-70420432 + B83-Tumor COSM1746537 c.958-1G>A p.? Unknown 11:70425331-70425331 + TCGA-06-5411-01 COSM3398100 c.211G>A p.E71K Substitution - Missense 11:70409880-70409880 + TCGA-26-6174-01 COSM3398103 c.712G>A p.V238M Substitution - Missense 11:70420432-70420432 + ICGC_0034 COSM218349 c.1202C>T p.T401M Substitution - Missense 11:70431216-70431216 + CSCC-47-T COSM1356669 c.932G>A p.G311E Substitution - Missense 11:70422970-70422970 + RK280_C01 COSM4944396 c.1517-5C>A p.? Unknown 11:70435021-70435021 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.596139;Hs.596140;Hs.596141;Hs.596142;Hs.596144;Hs.596150;Hs.596151;Hs.596152;Hs.596153;Hs.596158;Hs.596159;Hs.596162;Hs.596163;Hs.596164 11q13 164765 2466207|CGAP|BC008799|C/T|coding|Thr24Thr|239|Validated; 2466207|CGAP|BC033889|C/T|coding|Thr24Thr|247|Validated; 2466209|CGAP|BC008799|A/C|non-coding||3070|Validated; 2466209|CGAP|BC033889|A/C|non-coding||2195|Validated; 2466211|CGAP|BC008799|A/G|non-coding||2053|Candidate; 2466211|CGAP|BC033889|A/G|coding|Val514Met|1715|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G IntronicSNV . c.790+983A>G 11 70267599 CM A G Missense p.E146G c.437A>G 11 70261803 LGG A G Missense p.Y104C c.311A>G 11 70260667 LUSC A G Missense p.Y162C c.485A>G 11 70263146 HNSC A T Missense p.I55L c.163A>T 11 70255938 SCLC CAAGTAACAT - Frameshift p.S311Efs*81 c.931_940delAGTAACATCA 11 70275169 HNSC C A Missense p.Q151K c.451C>A 11 70261817 CM C A Missense p.Q151K c.451C>A 11 70261817 STAD C A Nonsense p.S380* c.1139C>A 11 70277370 LUSC CC TT SpliceDonorBlockSubstitution . c.1497_1498delinsTT 11 70281223 CM C G Missense p.Q216E c.646C>G 11 70265929 BLCA C T IntronicSNV . c.1499+4C>T 11 70281229 BLCA C T IntronicSNV . c.1778+20C>T 11 70281870 CM C T IntronicSNV . c.457+130C>T 11 70261953 CM C T IntronicSNV . c.791-37C>T 11 70269009 CM C T Missense p.A173V c.518C>T 11 70263179 HC C T Missense p.A315V c.944C>T 11 70275184 UCEC C T Missense p.S192F c.575C>T 11 70265858 CM C T Missense p.T364M c.1091C>T 11 70277322 PAAD C T Nonsense p.R168* c.502C>T 11 70263163 UCEC C T Synonymous p.A460A c.1380C>T 11 70279799 UCEC C T Synonymous p.G163G c.489C>T 11 70263150 STAD C T Synonymous p.G470G c.1410C>T 11 70281136 UCEC C T Synonymous p.I201I c.603C>T 11 70265886 CM C T Synonymous p.S294S c.882C>T 11 70271473 CM C T Synonymous p.V100V c.300C>T 11 70260656 HNSC G A IntronicSNV . c.1499+36G>A 11 70281261 HNSC G A Missense p.A370T c.1108G>A 11 70277339 STAD G A Missense p.E375K c.1123G>A 11 70277354 BRCA G A Missense p.E473K c.1417G>A 11 70281143 BLCA G A Missense p.E71K c.211G>A 11 70255986 GBM G A Missense p.G234E c.701G>A 11 70266527 LUSC G A Missense p.R602Q c.1805G>A 11 70282414 STAD G A Missense p.V238M c.712G>A 11 70266538 GBM G A Synonymous p.A332A c.996G>A 11 70275236 BRCA G A Synonymous p.E335E c.1005G>A 11 70275245 CM G A Synonymous p.P405P c.1215G>A 11 70279266 GBM G A Synonymous p.R279R c.837G>A 11 70269092 CLL G C Missense p.G274A c.821G>C 11 70269076 OV G C Missense p.G457R c.1369G>C 11 70279788 BRCA G C Missense p.G491R c.1471G>C 11 70281197 LUSC G C Missense p.G85A c.254G>C 11 70256029 BRCA G C Synonymous p.V367V c.1101G>C 11 70277332 BLCA G T IntronicSNV . c.1334-147G>T 11 70279606 NSCLC G T IntronicSNV . c.1499+6G>T 11 70281231 SCLC G T IntronicSNV . c.917-1590G>T 11 70273567 CLL G T Missense p.D455Y c.1363G>T 11 70279782 LUAD G T Missense p.K171N c.513G>T 11 70263174 LUAD G T Missense p.K70N c.210G>T 11 70255985 LUSC