Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 598468 598468 + Silent SNP G G A TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr11:598468G>A c.990G>A c.(988-990)acG>acA p.T330T ACC 11 607214 607214 + Missense_Mutation SNP A A T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr11:607214A>T c.1758A>T c.(1756-1758)caA>caT p.Q586H ACC 11 608624 608625 + Frame_Shift_Ins INS - - GACCGCTCCAG TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr11:608624_608625insGACCGCTCCAG c.3168_3169insGACCGCTCCAG c.(3169-3171)gacfs p.-1057fs ACC 11 610978 610978 + Missense_Mutation SNP G G A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr11:610978G>A c.4702G>A c.(4702-4704)Gag>Aag p.E1568K BLCA 11 591414 591414 + Missense_Mutation SNP C C G TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr11:591414C>G c.451C>G c.(451-453)Cta>Gta p.L151V BLCA 11 591423 591423 + Missense_Mutation SNP T T A TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr11:591423T>A c.460T>A c.(460-462)Tgc>Agc p.C154S BLCA 11 592637 592637 + Missense_Mutation SNP G G A TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr11:592637G>A c.583G>A c.(583-585)Gag>Aag p.E195K BLCA 11 596980 596980 + Silent SNP C C T TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr11:596980C>T c.678C>T c.(676-678)ttC>ttT p.F226F BLCA 11 597514 597514 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr11:597514G>A c.838G>A c.(838-840)Gag>Aag p.E280K BLCA 11 598428 598428 + Missense_Mutation SNP C C T TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr11:598428C>T c.950C>T c.(949-951)gCg>gTg p.A317V BLCA 11 598443 598443 + Missense_Mutation SNP C C G TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr11:598443C>G c.965C>G c.(964-966)aCt>aGt p.T322S BLCA 11 598454 598454 + Missense_Mutation SNP C C G TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr11:598454C>G c.976C>G c.(976-978)Cag>Gag p.Q326E BLCA 11 601682 601682 + Missense_Mutation SNP G G C TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chr11:601682G>C c.1133G>C c.(1132-1134)aGa>aCa p.R378T BLCA 11 605261 605261 + Missense_Mutation SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:605261C>T c.1295C>T c.(1294-1296)tCt>tTt p.S432F BLCA 11 607297 607297 + Missense_Mutation SNP G G A TCGA-C4-A0F7-01A-11D-A10S-08 TCGA-C4-A0F7-10A-01D-A10S-08 g.chr11:607297G>A c.1841G>A c.(1840-1842)cGg>cAg p.R614Q BLCA 11 607589 607589 + Silent SNP C C A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:607589C>A c.2133C>A c.(2131-2133)atC>atA p.I711I BLCA 11 607922 607922 + Silent SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:607922G>A c.2466G>A c.(2464-2466)acG>acA p.T822T BLCA 11 608431 608431 + Missense_Mutation SNP G G T TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr11:608431G>T c.2975G>T c.(2974-2976)cGg>cTg p.R992L BLCA 11 608501 608501 + Silent SNP A A G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr11:608501A>G c.3045A>G c.(3043-3045)ggA>ggG p.G1015G BLCA 11 608811 608811 + Missense_Mutation SNP C C T TCGA-5N-A9KI-01A-31D-A42E-08 TCGA-5N-A9KI-10A-01D-A42H-08 g.chr11:608811C>T c.3355C>T c.(3355-3357)Cgg>Tgg p.R1119W BLCA 11 608824 608824 + Missense_Mutation SNP G G A TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr11:608824G>A c.3368G>A c.(3367-3369)tGc>tAc p.C1123Y BLCA 11 609398 609398 + Silent SNP G G A TCGA-BT-A20V-01A-11D-A14W-08 TCGA-BT-A20V-11A-11D-A14W-08 g.chr11:609398G>A c.3942G>A c.(3940-3942)ctG>ctA p.L1314L BLCA 11 609574 609574 + Missense_Mutation SNP C C T TCGA-PQ-A6FI-01A-11D-A31L-08 TCGA-PQ-A6FI-10A-01D-A31J-08 g.chr11:609574C>T c.4118C>T c.(4117-4119)tCt>tTt p.S1373F BLCA 11 611697 611697 + Missense_Mutation SNP G G A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr11:611697G>A c.4870G>A c.(4870-4872)Gtg>Atg p.V1624M BRCA 11 591405 591405 + Missense_Mutation SNP G G A TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr11:591405G>A c.442G>A c.(442-444)Gat>Aat p.D148N BRCA 11 601669 601669 + Nonsense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:601669C>T c.1120C>T c.(1120-1122)Cga>Tga p.R374* BRCA 11 605238 605238 + Silent SNP G G A TCGA-E9-A1R7-01A-11D-A14K-09 TCGA-E9-A1R7-10A-01D-A14K-09 g.chr11:605238G>A c.1272G>A c.(1270-1272)gcG>gcA p.A424A BRCA 11 607853 607853 + Silent SNP G G C TCGA-A2-A0T3-01A-21D-A10Y-09 TCGA-A2-A0T3-10A-01D-A110-09 g.chr11:607853G>C c.2397G>C c.(2395-2397)acG>acC p.T799T BRCA 11 607938 607938 + Missense_Mutation SNP G G A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr11:607938G>A c.2482G>A c.(2482-2484)Gag>Aag p.E828K BRCA 11 608125 608125 + Missense_Mutation SNP C C T TCGA-AN-A0FX-01A-11W-A050-09 TCGA-AN-A0FX-10A-01W-A055-09 g.chr11:608125C>T c.2669C>T c.(2668-2670)aCa>aTa p.T890I BRCA 11 608991 608991 + Missense_Mutation SNP C C T TCGA-A1-A0SI-01A-11D-A142-09 TCGA-A1-A0SI-10B-01D-A142-09 g.chr11:608991C>T c.3535C>T c.(3535-3537)Cgg>Tgg p.R1179W BRCA 11 609477 609477 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr11:609477A>C c.4021A>C c.(4021-4023)Acc>Ccc p.T1341P BRCA 11 610989 610991 + In_Frame_Del DEL GGA GGA - TCGA-C8-A12O-01A-11D-A10Y-09 TCGA-C8-A12O-10A-01D-A110-09 g.chr11:610989_610991delGGA c.4713_4715delGGA c.(4711-4716)gtggag>gtg p.E1573del CESC 11 591399 591399 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:591399C>G c.436C>G c.(436-438)Cca>Gca p.P146A CESC 11 605255 605255 + Missense_Mutation SNP C C G TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr11:605255C>G c.1289C>G c.(1288-1290)tCt>tGt p.S430C CESC 11 606580 606580 + Silent SNP C C G TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr11:606580C>G c.1593C>G c.(1591-1593)ctC>ctG p.L531L CESC 11 607352 607352 + Silent SNP C C T TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr11:607352C>T c.1896C>T c.(1894-1896)ttC>ttT p.F632F CESC 11 608208 608208 + Missense_Mutation SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr11:608208G>C c.2752G>C c.(2752-2754)Gag>Cag p.E918Q CESC 11 608302 608302 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr11:608302G>A c.2846G>A c.(2845-2847)tGc>tAc p.C949Y CESC 11 610993 610993 + Missense_Mutation SNP G G A TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr11:610993G>A c.4717G>A c.(4717-4719)Gag>Aag p.E1573K COAD 11 582025 582025 + Missense_Mutation SNP G G T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:582025G>T c.158G>T c.(157-159)gGc>gTc p.G53V COAD 11 591435 591435 + Silent SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:591435C>A c.472C>A c.(472-474)Cga>Aga p.R158R COAD 11 592566 592566 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:592566T>C c.512T>C c.(511-513)gTg>gCg p.V171A COAD 11 592602 592602 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr11:592602C>T c.548C>T c.(547-549)cCg>cTg p.P183L COAD 11 601665 601665 + Silent SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:601665A>G c.1116A>G c.(1114-1116)caA>caG p.Q372Q COAD 11 605170 605170 + Missense_Mutation SNP C C A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr11:605170C>A c.1204C>A c.(1204-1206)Cct>Act p.P402T COAD 11 605710 605710 + Silent SNP C C T TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:605710C>T c.1440C>T c.(1438-1440)tcC>tcT p.S480S COAD 11 605711 605711 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:605711G>A c.1441G>A c.(1441-1443)Gtg>Atg p.V481M COAD 11 607394 607394 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:607394G>A c.1938G>A c.(1936-1938)gcG>gcA p.A646A COAD 11 607462 607462 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:607462C>A c.2006C>A c.(2005-2007)cCa>cAa p.P669Q COAD 11 608472 608472 + Missense_Mutation SNP A A C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:608472A>C c.3016A>C c.(3016-3018)Aag>Cag p.K1006Q COAD 11 608864 608864 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:608864G>A c.3408G>A c.(3406-3408)aaG>aaA p.K1136K COAD 11 609288 609288 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:609288G>A c.3832G>A c.(3832-3834)Gcc>Acc p.A1278T COAD 11 609628 609628 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:609628delC c.4172delC c.(4171-4173)accfs p.T1391fs COADREAD 11 582025 582025 + Missense_Mutation SNP G G T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:582025G>T c.158G>T c.(157-159)gGc>gTc p.G53V COADREAD 11 591435 591435 + Silent SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:591435C>A c.472C>A c.(472-474)Cga>Aga p.R158R COADREAD 11 592566 592566 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:592566T>C c.512T>C c.(511-513)gTg>gCg p.V171A COADREAD 11 592602 592602 + Missense_Mutation SNP C C T TCGA-AA-3994-01A-01W-1073-09 TCGA-AA-3994-10A-01W-1073-09 g.chr11:592602C>T c.548C>T c.(547-549)cCg>cTg p.P183L COADREAD 11 601665 601665 + Silent SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:601665A>G c.1116A>G c.(1114-1116)caA>caG p.Q372Q COADREAD 11 605170 605170 + Missense_Mutation SNP C C A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr11:605170C>A c.1204C>A c.(1204-1206)Cct>Act p.P402T COADREAD 11 605710 605710 + Silent SNP C C T TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:605710C>T c.1440C>T c.(1438-1440)tcC>tcT p.S480S COADREAD 11 605711 605711 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr11:605711G>A c.1441G>A c.(1441-1443)Gtg>Atg p.V481M COADREAD 11 607394 607394 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:607394G>A c.1938G>A c.(1936-1938)gcG>gcA p.A646A COADREAD 11 607462 607462 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:607462C>A c.2006C>A c.(2005-2007)cCa>cAa p.P669Q COADREAD 11 608472 608472 + Missense_Mutation SNP A A C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:608472A>C c.3016A>C c.(3016-3018)Aag>Cag p.K1006Q COADREAD 11 608864 608864 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:608864G>A c.3408G>A c.(3406-3408)aaG>aaA p.K1136K COADREAD 11 609068 609068 + Silent SNP G G A TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr11:609068G>A c.3612G>A c.(3610-3612)gcG>gcA p.A1204A COADREAD 11 609288 609288 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:609288G>A c.3832G>A c.(3832-3834)Gcc>Acc p.A1278T COADREAD 11 609553 609553 + Missense_Mutation SNP C C T TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr11:609553C>T c.4097C>T c.(4096-4098)gCg>gTg p.A1366V COADREAD 11 609628 609628 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:609628delC c.4172delC c.(4171-4173)accfs p.T1391fs DLBC 11 582056 582056 + Silent SNP G G A TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr11:582056G>A c.189G>A c.(187-189)gaG>gaA p.E63E DLBC 11 608546 608546 + Silent SNP G G A TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr11:608546G>A c.3090G>A c.(3088-3090)tcG>tcA p.S1030S ESCA 11 597555 597555 + Silent SNP G G A TCGA-L5-A4OQ-01A-11D-A27G-09 TCGA-L5-A4OQ-11A-12D-A27G-09 g.chr11:597555G>A c.879G>A c.(877-879)acG>acA p.T293T ESCA 11 601669 601669 + Nonsense_Mutation SNP C C T TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr11:601669C>T c.1120C>T c.(1120-1122)Cga>Tga p.R374* ESCA 11 608012 608012 + Silent SNP C C T TCGA-2H-A9GM-01A-11D-A37C-09 TCGA-2H-A9GM-11A-11D-A37F-09 g.chr11:608012C>T c.2556C>T c.(2554-2556)ccC>ccT p.P852P GBM 11 607162 607162 + Missense_Mutation SNP C C A TCGA-41-2572-01A-01D-1353-08 TCGA-41-2572-10A-01D-1353-08 g.chr11:607162C>A c.1706C>A c.(1705-1707)cCg>cAg p.P569Q GBM 11 607393 607393 + Missense_Mutation SNP C C T TCGA-28-2499-01A-01D-1494-08 TCGA-28-2499-10A-01D-1494-08 g.chr11:607393C>T c.1937C>T c.(1936-1938)gCg>gTg p.A646V GBM 11 608268 608268 + Missense_Mutation SNP C C T TCGA-41-2573-01A-01D-1495-08 TCGA-41-2573-10A-01D-1495-08 g.chr11:608268C>T c.2812C>T c.(2812-2814)Cca>Tca p.P938S GBM 11 608380 608380 + Missense_Mutation SNP A A T TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chr11:608380A>T c.2924A>T c.(2923-2925)gAc>gTc p.D975V GBMLGG 11 587330 587330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:587330G>A c.286G>A c.(286-288)Gct>Act p.A96T GBMLGG 11 587410 587410 + Silent SNP G G A TCGA-S9-A6UB-01A-21D-A33T-08 TCGA-S9-A6UB-10A-01D-A33W-08 g.chr11:587410G>A c.366G>A c.(364-366)acG>acA p.T122T GBMLGG 11 592586 592588 + In_Frame_Del DEL GAG GAG - TCGA-DU-A5TY-01A-11D-A289-08 TCGA-DU-A5TY-10A-01D-A289-08 g.chr11:592586_592588delGAG c.532_534delGAG c.(532-534)gagdel p.E181del GBMLGG 11 592614 592614 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:592614A>G c.560A>G c.(559-561)gAg>gGg p.E187G GBMLGG 11 607162 607162 + Missense_Mutation SNP C C A TCGA-41-2572-01A-01D-1353-08 TCGA-41-2572-10A-01D-1353-08 g.chr11:607162C>A c.1706C>A c.(1705-1707)cCg>cAg p.P569Q GBMLGG 11 607285 607285 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:607285C>T c.1829C>T c.(1828-1830)gCg>gTg p.A610V GBMLGG 11 607393 607393 + Missense_Mutation SNP C C T TCGA-28-2499-01A-01D-1494-08 TCGA-28-2499-10A-01D-1494-08 g.chr11:607393C>T c.1937C>T c.(1936-1938)gCg>gTg p.A646V GBMLGG 11 608157 608157 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:608157G>A c.2701G>A c.(2701-2703)Gcc>Acc p.A901T GBMLGG 11 608259 608259 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:608259C>T c.2803C>T c.(2803-2805)Cca>Tca p.P935S GBMLGG 11 608268 608268 + Missense_Mutation SNP C C T TCGA-41-2573-01A-01D-1495-08 TCGA-41-2573-10A-01D-1495-08 g.chr11:608268C>T c.2812C>T c.(2812-2814)Cca>Tca p.P938S GBMLGG 11 608380 608380 + Missense_Mutation SNP A A T TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chr11:608380A>T c.2924A>T c.(2923-2925)gAc>gTc p.D975V GBMLGG 11 608555 608555 + Silent SNP G G A TCGA-DU-7015-01A-11D-2024-08 TCGA-DU-7015-10B-01D-2024-08 g.chr11:608555G>A c.3099G>A c.(3097-3099)gcG>gcA p.A1033A GBMLGG 11 609157 609157 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:609157C>T c.3701C>T c.(3700-3702)aCg>aTg p.T1234M GBMLGG 11 609277 609277 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:609277T>G c.3821T>G c.(3820-3822)tTc>tGc p.F1274C HNSC 11 587346 587346 + Missense_Mutation SNP C C G TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr11:587346C>G c.302C>G c.(301-303)tCt>tGt p.S101C HNSC 11 587351 587351 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr11:587351G>A c.307G>A c.(307-309)Gat>Aat p.D103N HNSC 11 587453 587453 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr11:587453G>A c.409G>A c.(409-411)Gaa>Aaa p.E137K HNSC 11 592631 592631 + Missense_Mutation SNP G G A TCGA-F7-A50I-01A-11D-A28R-08 TCGA-F7-A50I-10A-01D-A28U-08 g.chr11:592631G>A c.577G>A c.(577-579)Gac>Aac p.D193N HNSC 11 596953 596953 + Silent SNP C C G TCGA-CN-A49A-01A-11D-A24D-08 TCGA-CN-A49A-10A-01D-A24F-08 g.chr11:596953C>G c.651C>G c.(649-651)ctC>ctG p.L217L HNSC 11 601588 601588 + Missense_Mutation SNP G G C TCGA-UF-A7JH-01A-21D-A34J-08 TCGA-UF-A7JH-10A-01D-A34M-08 g.chr11:601588G>C c.1039G>C c.(1039-1041)Gtg>Ctg p.V347L HNSC 11 605232 605232 + Silent SNP G G A TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr11:605232G>A c.1266G>A c.(1264-1266)ctG>ctA p.L422L HNSC 11 605263 605263 + Missense_Mutation SNP C C G TCGA-CX-7219-01A-11D-2012-08 TCGA-CX-7219-10A-01D-2013-08 g.chr11:605263C>G c.1297C>G c.(1297-1299)Ctg>Gtg p.L433V HNSC 11 606519 606519 + Missense_Mutation SNP C C G TCGA-CN-6013-01A-11D-1683-08 TCGA-CN-6013-10A-01D-1683-08 g.chr11:606519C>G c.1532C>G c.(1531-1533)tCg>tGg p.S511W HNSC 11 607230 607230 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:607230C>T c.1774C>T c.(1774-1776)Ccc>Tcc p.P592S HNSC 11 607244 607244 + Silent SNP G G A TCGA-CX-7086-01A-11D-2078-08 TCGA-CX-7086-10D-01D-2078-08 g.chr11:607244G>A c.1788G>A c.(1786-1788)gcG>gcA p.A596A HNSC 11 607585 607590 + In_Frame_Del DEL GCATCA GCATCA - TCGA-MT-A67D-01A-31D-A30E-08 TCGA-MT-A67D-10A-01D-A30H-08 g.chr11:607585_607590delGCATCA c.2129_2134delGCATCA c.(2128-2136)tgcatcagc>tgc p.IS711del HNSC 11 607619 607619 + Silent SNP G G A TCGA-H7-A6C5-01A-11D-A30E-08 TCGA-H7-A6C5-10A-01D-A30H-08 g.chr11:607619G>A c.2163G>A c.(2161-2163)ggG>ggA p.G721G HNSC 11 607897 607897 + Missense_Mutation SNP C C T TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chr11:607897C>T c.2441C>T c.(2440-2442)tCa>tTa p.S814L HNSC 11 608214 608214 + Missense_Mutation SNP G G C TCGA-H7-8501-01A-11D-2394-08 TCGA-H7-8501-10A-01D-2394-08 g.chr11:608214G>C c.2758G>C c.(2758-2760)Gag>Cag p.E920Q HNSC 11 608731 608731 + Missense_Mutation SNP G G T TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr11:608731G>T c.3275G>T c.(3274-3276)cGg>cTg p.R1092L HNSC 11 608969 608969 + Missense_Mutation SNP G G T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr11:608969G>T c.3513G>T c.(3511-3513)agG>agT p.R1171S HNSC 11 608998 608998 + Missense_Mutation SNP G G T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:608998G>T c.3542G>T c.(3541-3543)cGt>cTt p.R1181L HNSC 11 609228 609228 + Missense_Mutation SNP G G A TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr11:609228G>A c.3772G>A c.(3772-3774)Gac>Aac p.D1258N HNSC 11 609574 609574 + Missense_Mutation SNP C C G TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr11:609574C>G c.4118C>G c.(4117-4119)tCt>tGt p.S1373C HNSC 11 611008 611008 + Missense_Mutation SNP A A T TCGA-HD-7832-01A-11D-2129-08 TCGA-HD-7832-10A-01D-2129-08 g.chr11:611008A>T c.4732A>T c.(4732-4734)Atc>Ttc p.I1578F HNSC 11 611692 611692 + Missense_Mutation SNP C C T TCGA-HD-7229-01A-11D-2012-08 TCGA-HD-7229-10A-01D-2013-08 g.chr11:611692C>T c.4865C>T c.(4864-4866)gCg>gTg p.A1622V KICH 11 605169 605169 + Missense_Mutation SNP G G T TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr11:605169G>T c.1203G>T c.(1201-1203)agG>agT p.R401S KIPAN 11 598434 598434 + Missense_Mutation SNP G G A TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr11:598434G>A c.956G>A c.(955-957)gGc>gAc p.G319D KIPAN 11 601639 601639 + Missense_Mutation SNP T T C TCGA-BQ-5885-01A-11D-1589-08 TCGA-BQ-5885-11A-01D-1589-08 g.chr11:601639T>C c.1090T>C c.(1090-1092)Tca>Cca p.S364P KIPAN 11 605169 605169 + Missense_Mutation SNP G G T TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr11:605169G>T c.1203G>T c.(1201-1203)agG>agT p.R401S KIPAN 11 605692 605692 + Silent SNP C C T TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr11:605692C>T c.1422C>T c.(1420-1422)ccC>ccT p.P474P KIPAN 11 608267 608267 + Silent SNP C C A TCGA-BP-5180-01A-01D-1429-08 TCGA-BP-5180-11A-01D-1429-08 g.chr11:608267C>A c.2811C>A c.(2809-2811)ccC>ccA p.P937P KIPAN 11 608822 608822 + Silent SNP G G A TCGA-CW-5589-01A-01D-1534-10 TCGA-CW-5589-11A-01D-1535-10 g.chr11:608822G>A c.3366G>A c.(3364-3366)gaG>gaA p.E1122E KIRC 11 608267 608267 + Silent SNP C C A TCGA-BP-5180-01A-01D-1429-08 TCGA-BP-5180-11A-01D-1429-08 g.chr11:608267C>A c.2811C>A c.(2809-2811)ccC>ccA p.P937P KIRC 11 608822 608822 + Silent SNP G G A TCGA-CW-5589-01A-01D-1534-10 TCGA-CW-5589-11A-01D-1535-10 g.chr11:608822G>A c.3366G>A c.(3364-3366)gaG>gaA p.E1122E KIRP 11 598434 598434 + Missense_Mutation SNP G G A TCGA-SX-A71S-01A-11D-A33Q-10 TCGA-SX-A71S-10A-01D-A33Q-10 g.chr11:598434G>A c.956G>A c.(955-957)gGc>gAc p.G319D KIRP 11 601639 601639 + Missense_Mutation SNP T T C TCGA-BQ-5885-01A-11D-1589-08 TCGA-BQ-5885-11A-01D-1589-08 g.chr11:601639T>C c.1090T>C c.(1090-1092)Tca>Cca p.S364P KIRP 11 605692 605692 + Silent SNP C C T TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr11:605692C>T c.1422C>T c.(1420-1422)ccC>ccT p.P474P LGG 11 587330 587330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:587330G>A c.286G>A c.(286-288)Gct>Act p.A96T LGG 11 587410 587410 + Silent SNP G G A TCGA-S9-A6UB-01A-21D-A33T-08 TCGA-S9-A6UB-10A-01D-A33W-08 g.chr11:587410G>A c.366G>A c.(364-366)acG>acA p.T122T LGG 11 592586 592588 + In_Frame_Del DEL GAG GAG - TCGA-DU-A5TY-01A-11D-A289-08 TCGA-DU-A5TY-10A-01D-A289-08 g.chr11:592586_592588delGAG c.532_534delGAG c.(532-534)gagdel p.E181del LGG 11 592614 592614 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:592614A>G c.560A>G c.(559-561)gAg>gGg p.E187G LGG 11 607285 607285 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:607285C>T c.1829C>T c.(1828-1830)gCg>gTg p.A610V LGG 11 608157 608157 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:608157G>A c.2701G>A c.(2701-2703)Gcc>Acc p.A901T LGG 11 608259 608259 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:608259C>T c.2803C>T c.(2803-2805)Cca>Tca p.P935S LGG 11 608555 608555 + Silent SNP G G A TCGA-DU-7015-01A-11D-2024-08 TCGA-DU-7015-10B-01D-2024-08 g.chr11:608555G>A c.3099G>A c.(3097-3099)gcG>gcA p.A1033A LGG 11 609157 609157 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:609157C>T c.3701C>T c.(3700-3702)aCg>aTg p.T1234M LGG 11 609277 609277 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:609277T>G c.3821T>G c.(3820-3822)tTc>tGc p.F1274C LIHC 11 587380 587380 + Silent SNP C C A TCGA-G3-A5SJ-01A-11D-A27I-10 TCGA-G3-A5SJ-10A-01D-A27I-10 g.chr11:587380C>A c.336C>A c.(334-336)ctC>ctA p.L112L LIHC 11 592654 592654 + Silent SNP C C G TCGA-RC-A7SF-01A-11D-A34Z-10 TCGA-RC-A7SF-10A-01D-A34Z-10 g.chr11:592654C>G c.600C>G c.(598-600)ctC>ctG p.L200L LIHC 11 597422 597422 + Missense_Mutation SNP T T G TCGA-DD-AAEH-01A-11D-A40R-10 TCGA-DD-AAEH-10A-01D-A40U-10 g.chr11:597422T>G c.746T>G c.(745-747)gTc>gGc p.V249G LIHC 11 606503 606503 + Silent SNP C C T TCGA-DD-A73G-01A-22D-A32G-10 TCGA-DD-A73G-10A-01D-A32G-10 g.chr11:606503C>T c.1516C>T c.(1516-1518)Ctg>Ttg p.L506L LIHC 11 607103 607103 + Silent SNP C C A TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:607103C>A c.1647C>A c.(1645-1647)tcC>tcA p.S549S LIHC 11 608299 608299 + Missense_Mutation SNP C C T TCGA-BC-A10Y-01A-11D-A12Z-10 TCGA-BC-A10Y-11A-11D-A12Z-10 g.chr11:608299C>T c.2843C>T c.(2842-2844)tCt>tTt p.S948F LIHC 11 608998 608998 + Missense_Mutation SNP G G T TCGA-MI-A75C-01A-11D-A32G-10 TCGA-MI-A75C-10A-01D-A32G-10 g.chr11:608998G>T c.3542G>T c.(3541-3543)cGt>cTt p.R1181L LIHC 11 609135 609135 + Missense_Mutation SNP C C G TCGA-CC-A7IG-01A-11D-A33K-10 TCGA-CC-A7IG-10A-01D-A33K-10 g.chr11:609135C>G c.3679C>G c.(3679-3681)Cat>Gat p.H1227D LIHC 11 609548 609548 + Silent SNP G G A TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:609548G>A c.4092G>A c.(4090-4092)gcG>gcA p.A1364A LIHC 11 610529 610529 + Missense_Mutation SNP C C T TCGA-KR-A7K7-01A-11D-A33K-10 TCGA-KR-A7K7-10A-01D-A33K-10 g.chr11:610529C>T c.4445C>T c.(4444-4446)cCg>cTg p.P1482L LIHC 11 610607 610607 + Missense_Mutation SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:610607C>T c.4523C>T c.(4522-4524)cCg>cTg p.P1508L LIHC 11 611702 611702 + Missense_Mutation SNP C C A TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr11:611702C>A c.4875C>A c.(4873-4875)gaC>gaA p.D1625E LUAD 11 587399 587399 + Missense_Mutation SNP G G C TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr11:587399G>C c.355G>C c.(355-357)Gcc>Ccc p.A119P LUAD 11 591441 591441 + Missense_Mutation SNP C C G TCGA-MP-A4TI-01A-21D-A24P-08 TCGA-MP-A4TI-10A-01D-A24P-08 g.chr11:591441C>G c.478C>G c.(478-480)Caa>Gaa p.Q160E LUAD 11 591448 591448 + Missense_Mutation SNP G G T TCGA-62-8394-01A-11D-2323-08 TCGA-62-8394-10A-01D-2323-08 g.chr11:591448G>T c.485G>T c.(484-486)gGt>gTt p.G162V LUAD 11 605711 605711 + Missense_Mutation SNP G G T TCGA-J2-A4AG-01A-11D-A24D-08 TCGA-J2-A4AG-10A-01D-A24F-08 g.chr11:605711G>T c.1441G>T c.(1441-1443)Gtg>Ttg p.V481L LUAD 11 607393 607393 + Missense_Mutation SNP C C T TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr11:607393C>T c.1937C>T c.(1936-1938)gCg>gTg p.A646V LUAD 11 607913 607913 + Missense_Mutation SNP C C G TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr11:607913C>G c.2457C>G c.(2455-2457)atC>atG p.I819M LUAD 11 608054 608064 + Frame_Shift_Del DEL CAGCCCGAAGG CAGCCCGAAGG - TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr11:608054_608064delCAGCCCGAAGG c.2598_2608delCAGCCCGAAGG c.(2596-2610)aacagcccgaaggccfs p.SPKA867fs LUAD 11 608231 608231 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr11:608231C>A c.2775C>A c.(2773-2775)agC>agA p.S925R LUAD 11 608234 608234 + Missense_Mutation SNP G G T TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr11:608234G>T c.2778G>T c.(2776-2778)caG>caT p.Q926H LUAD 11 608852 608852 + Silent SNP C C G TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr11:608852C>G c.3396C>G c.(3394-3396)ctC>ctG p.L1132L LUAD 11 609112 609112 + Missense_Mutation SNP G G A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:609112G>A c.3656G>A c.(3655-3657)aGg>aAg p.R1219K LUAD 11 609288 609288 + Missense_Mutation SNP G G A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr11:609288G>A c.3832G>A c.(3832-3834)Gcc>Acc p.A1278T LUAD 11 609458 609458 + Silent SNP C C T TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr11:609458C>T c.4002C>T c.(4000-4002)ccC>ccT p.P1334P LUAD 11 611697 611697 + Missense_Mutation SNP G G A TCGA-69-8254-01A-11D-2284-08 TCGA-69-8254-10A-01D-2284-08 g.chr11:611697G>A c.4870G>A c.(4870-4872)Gtg>Atg p.V1624M LUSC 11 601622 601622 + Missense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr11:601622C>G c.1073C>G c.(1072-1074)tCc>tGc p.S358C LUSC 11 607998 607998 + Missense_Mutation SNP G G A TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr11:607998G>A c.2542G>A c.(2542-2544)Gag>Aag p.E848K LUSC 11 608235 608235 + Missense_Mutation SNP G G T TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr11:608235G>T c.2779G>T c.(2779-2781)Ggc>Tgc p.G927C LUSC 11 608509 608509 + Missense_Mutation SNP G G T TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chr11:608509G>T c.3053G>T c.(3052-3054)cGc>cTc p.R1018L LUSC 11 608828 608828 + Silent SNP C C T TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr11:608828C>T c.3372C>T c.(3370-3372)tcC>tcT p.S1124S LUSC 11 611692 611692 + Missense_Mutation SNP C C G TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr11:611692C>G c.4865C>G c.(4864-4866)gCg>gGg p.A1622G OV 11 592610 592610 + Missense_Mutation SNP T T A TCGA-29-1703-01A-01W-0633-09 TCGA-29-1703-10A-01W-0633-09 g.chr11:592610T>A c.556T>A c.(556-558)Tgt>Agt p.C186S PAAD 11 587346 587346 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:587346C>A c.302C>A c.(301-303)tCt>tAt p.S101Y PAAD 11 592586 592588 + In_Frame_Del DEL GAG GAG - TCGA-2J-AABP-01A-11D-A40W-08 TCGA-2J-AABP-10A-01D-A40W-08 g.chr11:592586_592588delGAG c.532_534delGAG c.(532-534)gagdel p.E181del PAAD 11 592586 592588 + In_Frame_Del DEL GAG GAG - TCGA-3A-A9IR-01A-11D-A38G-08 TCGA-3A-A9IR-10A-01D-A38J-08 g.chr11:592586_592588delGAG c.532_534delGAG c.(532-534)gagdel p.E181del PAAD 11 592586 592588 + In_Frame_Del DEL GAG GAG - TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr11:592586_592588delGAG c.532_534delGAG c.(532-534)gagdel p.E181del PCPG 11 605191 605191 + Missense_Mutation SNP C C T TCGA-QR-A70P-01A-11D-A35D-08 TCGA-QR-A70P-10A-01D-A35B-08 g.chr11:605191C>T c.1225C>T c.(1225-1227)Ccg>Tcg p.P409S PRAD 11 581559 581559 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:581559C>T c.47C>T c.(46-48)cCg>cTg p.P16L PRAD 11 597506 597506 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:597506G>A c.830G>A c.(829-831)cGg>cAg p.R277Q PRAD 11 607296 607296 + Silent SNP C C A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr11:607296C>A c.1840C>A c.(1840-1842)Cgg>Agg p.R614R PRAD 11 608013 608013 + Missense_Mutation SNP G G A TCGA-KK-A59Y-01A-11D-A26M-08 TCGA-KK-A59Y-11A-11D-A26K-08 g.chr11:608013G>A c.2557G>A c.(2557-2559)Ggc>Agc p.G853S READ 11 609068 609068 + Silent SNP G G A TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr11:609068G>A c.3612G>A c.(3610-3612)gcG>gcA p.A1204A READ 11 609553 609553 + Missense_Mutation SNP C C T TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr11:609553C>T c.4097C>T c.(4096-4098)gCg>gTg p.A1366V SARC 11 591456 591456 + Missense_Mutation SNP A A G TCGA-DX-A8BZ-01A-11D-A37C-09 TCGA-DX-A8BZ-10A-01D-A37F-09 g.chr11:591456A>G c.493A>G c.(493-495)Atc>Gtc p.I165V SARC 11 598385 598385 + Missense_Mutation SNP C C T TCGA-X6-A8C6-01A-11D-A36J-09 TCGA-X6-A8C6-10A-01D-A36M-09 g.chr11:598385C>T c.907C>T c.(907-909)Cgc>Tgc p.R303C SARC 11 605246 605246 + Missense_Mutation SNP G G T TCGA-3B-A9I1-01A-11D-A38Z-09 TCGA-3B-A9I1-10A-01D-A38Z-09 g.chr11:605246G>T c.1280G>T c.(1279-1281)gGa>gTa p.G427V SARC 11 610995 610995 + Missense_Mutation SNP G G C TCGA-N1-A6IA-01A-12D-A32I-09 TCGA-N1-A6IA-11A-11D-A32I-09 g.chr11:610995G>C c.4719G>C c.(4717-4719)gaG>gaC p.E1573D SKCM 11 587263 587263 + Silent SNP C C T TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr11:587263C>T c.219C>T c.(217-219)tcC>tcT p.S73S SKCM 11 587401 587401 + Silent SNP C C A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:587401C>A c.357C>A c.(355-357)gcC>gcA p.A119A SKCM 11 587429 587429 + Missense_Mutation SNP T T G TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr11:587429T>G c.385T>G c.(385-387)Tac>Gac p.Y129D SKCM 11 591394 591394 + Missense_Mutation SNP C C T TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr11:591394C>T c.431C>T c.(430-432)tCc>tTc p.S144F SKCM 11 591435 591435 + Nonsense_Mutation SNP C C T TCGA-EE-A3AD-06A-11D-A196-08 TCGA-EE-A3AD-10A-01D-A198-08 g.chr11:591435C>T c.472C>T c.(472-474)Cga>Tga p.R158* SKCM 11 597425 597425 + Missense_Mutation SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr11:597425C>T c.749C>T c.(748-750)tCc>tTc p.S250F SKCM 11 605145 605145 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:605145C>T c.1179C>T c.(1177-1179)atC>atT p.I393I SKCM 11 605665 605665 + Silent SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr11:605665C>T c.1395C>T c.(1393-1395)tcC>tcT p.S465S SKCM 11 607121 607121 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:607121C>T c.1665C>T c.(1663-1665)ttC>ttT p.F555F SKCM 11 607444 607444 + Missense_Mutation SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr11:607444C>T c.1988C>T c.(1987-1989)cCg>cTg p.P663L SKCM 11 607720 607720 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr11:607720C>T c.2264C>T c.(2263-2265)tCc>tTc p.S755F SKCM 11 607766 607766 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:607766C>T c.2310C>T c.(2308-2310)gtC>gtT p.V770V SKCM 11 608886 608886 + Missense_Mutation SNP G G A TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr11:608886G>A c.3430G>A c.(3430-3432)Gag>Aag p.E1144K SKCM 11 608893 608893 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr11:608893C>T c.3437C>T c.(3436-3438)cCa>cTa p.P1146L SKCM 11 609185 609185 + Silent SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr11:609185C>T c.3729C>T c.(3727-3729)ccC>ccT p.P1243P SKCM 11 609256 609256 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr11:609256C>T c.3800C>T c.(3799-3801)gCc>gTc p.A1267V SKCM 11 609257 609257 + Silent SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr11:609257C>T c.3801C>T c.(3799-3801)gcC>gcT p.A1267A SKCM 11 609395 609395 + Silent SNP C C T TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr11:609395C>T c.3939C>T c.(3937-3939)agC>agT p.S1313S SKCM 11 609396 609396 + Silent SNP C C T TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr11:609396C>T c.3940C>T c.(3940-3942)Ctg>Ttg p.L1314L SKCM 11 609451 609451 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:609451C>T c.3995C>T c.(3994-3996)tCg>tTg p.S1332L SKCM 11 611069 611069 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:611069A>G c.4793A>G c.(4792-4794)aAg>aGg p.K1598R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 11 601624 601624 single base substitution G A exon_variant AML-US 11 601624 601624 single base substitution G A missense_variant A355T 1063G>A AML-US 11 601624 601624 single base substitution G A missense_variant A358T 1072G>A AML-US 11 601624 601624 single base substitution G A missense_variant A359T 1075G>A AML-US 11 601624 601624 single base substitution G A upstream_gene_variant BLCA-CN 11 611029 611029 single base substitution A G 3_prime_UTR_variant BLCA-CN 11 611029 611029 single base substitution A G downstream_gene_variant BLCA-CN 11 611029 611029 single base substitution A G missense_variant R1581G 4741A>G BLCA-CN 11 611029 611029 single base substitution A G missense_variant R1583G 4747A>G BLCA-CN 11 611029 611029 single base substitution A G missense_variant R1584G 4750A>G BLCA-CN 11 611029 611029 single base substitution A G missense_variant R1585G 4753A>G BLCA-US 11 597514 597514 single base substitution G A exon_variant BLCA-US 11 597514 597514 single base substitution G A missense_variant E276K 826G>A BLCA-US 11 597514 597514 single base substitution G A missense_variant E279K 835G>A BLCA-US 11 597514 597514 single base substitution G A missense_variant E280K 838G>A BLCA-US 11 597514 597514 single base substitution G A upstream_gene_variant BLCA-US 11 607297 607297 single base substitution G A downstream_gene_variant BLCA-US 11 607297 607297 single base substitution G A exon_variant BLCA-US 11 607297 607297 single base substitution G A missense_variant R610Q 1829G>A BLCA-US 11 607297 607297 single base substitution G A missense_variant R612Q 1835G>A BLCA-US 11 607297 607297 single base substitution G A missense_variant R613Q 1838G>A BLCA-US 11 607297 607297 single base substitution G A missense_variant R614Q 1841G>A BLCA-US 11 608824 608824 single base substitution G A downstream_gene_variant BLCA-US 11 608824 608824 single base substitution G A exon_variant BLCA-US 11 608824 608824 single base substitution G A missense_variant C1119Y 3356G>A BLCA-US 11 608824 608824 single base substitution G A missense_variant C1121Y 3362G>A BLCA-US 11 608824 608824 single base substitution G A missense_variant C1122Y 3365G>A BLCA-US 11 608824 608824 single base substitution G A missense_variant C1123Y 3368G>A BLCA-US 11 612784 612784 single base substitution C A downstream_gene_variant BOCA-FR 11 574037 574037 single base substitution G C upstream_gene_variant BRCA-EU 11 571649 571649 single base substitution G A upstream_gene_variant BRCA-EU 11 573441 573441 single base substitution C T upstream_gene_variant BRCA-EU 11 574034 574034 single base substitution A G upstream_gene_variant BRCA-EU 11 574697 574697 single base substitution C T upstream_gene_variant BRCA-EU 11 577366 577366 single base substitution G A intron_variant BRCA-EU 11 578829 578829 single base substitution G A intron_variant BRCA-EU 11 581889 581889 single base substitution G A intron_variant BRCA-EU 11 583117 583117 single base substitution G A intron_variant BRCA-EU 11 584169 584169 single base substitution C T intron_variant BRCA-EU 11 584840 584840 single base substitution C T intron_variant BRCA-EU 11 585765 585765 single base substitution C G intron_variant BRCA-EU 11 588147 588147 single base substitution C T intron_variant BRCA-EU 11 588471 588471 single base substitution C G intron_variant BRCA-EU 11 588589 588589 single base substitution G A intron_variant BRCA-EU 11 588692 588692 insertion of <=200bp - T intron_variant BRCA-EU 11 591948 591948 single base substitution C A intron_variant BRCA-EU 11 593815 593815 single base substitution G A intron_variant BRCA-EU 11 594145 594145 single base substitution C T intron_variant BRCA-EU 11 594217 594217 single base substitution G C intron_variant BRCA-EU 11 595962 595962 single base substitution G C intron_variant BRCA-EU 11 596570 596570 single base substitution C G intron_variant BRCA-EU 11 599533 599533 single base substitution C G intron_variant BRCA-EU 11 599533 599533 single base substitution C G upstream_gene_variant BRCA-EU 11 600738 600738 single base substitution G A intron_variant BRCA-EU 11 600738 600738 single base substitution G A upstream_gene_variant BRCA-EU 11 605654 605654 single base substitution C T exon_variant BRCA-EU 11 605654 605654 single base substitution C T missense_variant R458W 1372C>T BRCA-EU 11 605654 605654 single base substitution C T missense_variant R460W 1378C>T BRCA-EU 11 605654 605654 single base substitution C T missense_variant R461W 1381C>T BRCA-EU 11 605654 605654 single base substitution C T missense_variant R462W 1384C>T BRCA-EU 11 606703 606703 deletion of <=200bp G - exon_variant BRCA-EU 11 606703 606703 deletion of <=200bp G - intron_variant BRCA-EU 11 606849 606849 single base substitution T G downstream_gene_variant BRCA-EU 11 606849 606849 single base substitution T G intron_variant BRCA-EU 11 608837 608837 single base substitution C A downstream_gene_variant BRCA-EU 11 608837 608837 single base substitution C A exon_variant BRCA-EU 11 608837 608837 single base substitution C A missense_variant S1123R 3369C>A BRCA-EU 11 608837 608837 single base substitution C A missense_variant S1125R 3375C>A BRCA-EU 11 608837 608837 single base substitution C A missense_variant S1126R 3378C>A BRCA-EU 11 608837 608837 single base substitution C A missense_variant S1127R 3381C>A BRCA-EU 11 609280 609280 single base substitution C T downstream_gene_variant BRCA-EU 11 609280 609280 single base substitution C T exon_variant BRCA-EU 11 609280 609280 single base substitution C T missense_variant S1271L 3812C>T BRCA-EU 11 609280 609280 single base substitution C T missense_variant S1273L 3818C>T BRCA-EU 11 609280 609280 single base substitution C T missense_variant S1274L 3821C>T BRCA-EU 11 609280 609280 single base substitution C T missense_variant S1275L 3824C>T BRCA-EU 11 609654 609654 single base substitution G C downstream_gene_variant BRCA-EU 11 609654 609654 single base substitution G C exon_variant BRCA-EU 11 609654 609654 single base substitution G C missense_variant V1396L 4186G>C BRCA-EU 11 609654 609654 single base substitution G C missense_variant V1398L 4192G>C BRCA-EU 11 609654 609654 single base substitution G C missense_variant V1399L 4195G>C BRCA-EU 11 609654 609654 single base substitution G C missense_variant V1400L 4198G>C BRCA-EU 11 610144 610144 single base substitution C G downstream_gene_variant BRCA-EU 11 610144 610144 single base substitution C G intron_variant BRCA-EU 11 612269 612269 single base substitution C G downstream_gene_variant BRCA-EU 11 612653 612653 single base substitution G A downstream_gene_variant BRCA-EU 11 613493 613493 deletion of <=200bp G - downstream_gene_variant BRCA-EU 11 614123 614123 single base substitution C G downstream_gene_variant BRCA-EU 11 615592 615592 single base substitution G T downstream_gene_variant BRCA-EU 11 616448 616448 single base substitution C T downstream_gene_variant BRCA-EU 11 617023 617023 single base substitution C G downstream_gene_variant BRCA-FR 11 584840 584840 single base substitution C T intron_variant BRCA-FR 11 588471 588471 single base substitution C G intron_variant BRCA-FR 11 593943 593943 single base substitution C T intron_variant BRCA-FR 11 609622 609622 single base substitution C T downstream_gene_variant BRCA-FR 11 609622 609622 single base substitution C T exon_variant BRCA-FR 11 609622 609622 single base substitution C T missense_variant S1385L 4154C>T BRCA-FR 11 609622 609622 single base substitution C T missense_variant S1387L 4160C>T BRCA-FR 11 609622 609622 single base substitution C T missense_variant S1388L 4163C>T BRCA-FR 11 609622 609622 single base substitution C T missense_variant S1389L 4166C>T BRCA-FR 11 616193 616193 single base substitution T G downstream_gene_variant BRCA-KR 11 587389 587389 single base substitution C T exon_variant BRCA-KR 11 587389 587389 single base substitution C T synonymous_variant F111F 333C>T BRCA-KR 11 587389 587389 single base substitution C T synonymous_variant F114F 342C>T BRCA-KR 11 587389 587389 single base substitution C T synonymous_variant F115F 345C>T BRCA-KR 11 612717 612717 single base substitution G C downstream_gene_variant BRCA-UK 11 611286 611286 single base substitution G A downstream_gene_variant BRCA-UK 11 611286 611286 single base substitution G A intron_variant BRCA-US 11 591405 591405 single base substitution G A exon_variant BRCA-US 11 591405 591405 single base substitution G A missense_variant D144N 430G>A BRCA-US 11 591405 591405 single base substitution G A missense_variant D147N 439G>A BRCA-US 11 591405 591405 single base substitution G A missense_variant D148N 442G>A BRCA-US 11 601669 601669 single base substitution C T exon_variant BRCA-US 11 601669 601669 single base substitution C T stop_gained R370* 1108C>T BRCA-US 11 601669 601669 single base substitution C T stop_gained R373* 1117C>T BRCA-US 11 601669 601669 single base substitution C T stop_gained R374* 1120C>T BRCA-US 11 605238 605238 single base substitution G A exon_variant BRCA-US 11 605238 605238 single base substitution G A synonymous_variant A420A 1260G>A BRCA-US 11 605238 605238 single base substitution G A synonymous_variant A423A 1269G>A BRCA-US 11 605238 605238 single base substitution G A synonymous_variant A424A 1272G>A BRCA-US 11 607853 607853 single base substitution G C downstream_gene_variant BRCA-US 11 607853 607853 single base substitution G C exon_variant BRCA-US 11 607853 607853 single base substitution G C synonymous_variant T795T 2385G>C BRCA-US 11 607853 607853 single base substitution G C synonymous_variant T797T 2391G>C BRCA-US 11 607853 607853 single base substitution G C synonymous_variant T798T 2394G>C BRCA-US 11 607853 607853 single base substitution G C synonymous_variant T799T 2397G>C BRCA-US 11 607938 607938 single base substitution G A downstream_gene_variant BRCA-US 11 607938 607938 single base substitution G A exon_variant BRCA-US 11 607938 607938 single base substitution G A missense_variant E824K 2470G>A BRCA-US 11 607938 607938 single base substitution G A missense_variant E826K 2476G>A BRCA-US 11 607938 607938 single base substitution G A missense_variant E827K 2479G>A BRCA-US 11 607938 607938 single base substitution G A missense_variant E828K 2482G>A BRCA-US 11 608125 608125 single base substitution C T downstream_gene_variant BRCA-US 11 608125 608125 single base substitution C T exon_variant BRCA-US 11 608125 608125 single base substitution C T missense_variant T886I 2657C>T BRCA-US 11 608125 608125 single base substitution C T missense_variant T888I 2663C>T BRCA-US 11 608125 608125 single base substitution C T missense_variant T889I 2666C>T BRCA-US 11 608125 608125 single base substitution C T missense_variant T890I 2669C>T BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - downstream_gene_variant BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - exon_variant BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1012R BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1014R BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1015R BRCA-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1016R BRCA-US 11 608991 608991 single base substitution C T downstream_gene_variant BRCA-US 11 608991 608991 single base substitution C T exon_variant BRCA-US 11 608991 608991 single base substitution C T missense_variant R1175W 3523C>T BRCA-US 11 608991 608991 single base substitution C T missense_variant R1177W 3529C>T BRCA-US 11 608991 608991 single base substitution C T missense_variant R1178W 3532C>T BRCA-US 11 608991 608991 single base substitution C T missense_variant R1179W 3535C>T BRCA-US 11 609477 609477 single base substitution A C downstream_gene_variant BRCA-US 11 609477 609477 single base substitution A C exon_variant BRCA-US 11 609477 609477 single base substitution A C missense_variant T1337P 4009A>C BRCA-US 11 609477 609477 single base substitution A C missense_variant T1339P 4015A>C BRCA-US 11 609477 609477 single base substitution A C missense_variant T1340P 4018A>C BRCA-US 11 609477 609477 single base substitution A C missense_variant T1341P 4021A>C BRCA-US 11 610989 610991 deletion of <=200bp GGA - 3_prime_UTR_variant BRCA-US 11 610989 610991 deletion of <=200bp GGA - downstream_gene_variant BRCA-US 11 610989 610991 deletion of <=200bp GGA - inframe_deletion VE1567V BRCA-US 11 610989 610991 deletion of <=200bp GGA - inframe_deletion VE1569V BRCA-US 11 610989 610991 deletion of <=200bp GGA - inframe_deletion VE1570V BRCA-US 11 610989 610991 deletion of <=200bp GGA - inframe_deletion VE1571V BRCA-US 11 611789 611789 single base substitution C T 3_prime_UTR_variant BRCA-US 11 611789 611789 single base substitution C T downstream_gene_variant BRCA-US 11 612739 612739 deletion of <=200bp A - downstream_gene_variant BRCA-US 11 615281 615281 single base substitution G A downstream_gene_variant BTCA-JP 11 587385 587385 single base substitution C T exon_variant BTCA-JP 11 587385 587385 single base substitution C T missense_variant A110V 329C>T BTCA-JP 11 587385 587385 single base substitution C T missense_variant A113V 338C>T BTCA-JP 11 587385 587385 single base substitution C T missense_variant A114V 341C>T BTCA-JP 11 596964 596964 single base substitution C T exon_variant BTCA-JP 11 596964 596964 single base substitution C T missense_variant P217L 650C>T BTCA-JP 11 596964 596964 single base substitution C T missense_variant P220L 659C>T BTCA-JP 11 596964 596964 single base substitution C T missense_variant P221L 662C>T BTCA-JP 11 596964 596964 single base substitution C T upstream_gene_variant BTCA-JP 11 598578 598578 single base substitution C T intron_variant BTCA-JP 11 598578 598578 single base substitution C T upstream_gene_variant BTCA-JP 11 607098 607098 single base substitution C G downstream_gene_variant BTCA-JP 11 607098 607098 single base substitution C G exon_variant BTCA-JP 11 607098 607098 single base substitution C G missense_variant L544V 1630C>G BTCA-JP 11 607098 607098 single base substitution C G missense_variant L546V 1636C>G BTCA-JP 11 607098 607098 single base substitution C G missense_variant L547V 1639C>G BTCA-JP 11 607098 607098 single base substitution C G missense_variant L548V 1642C>G BTCA-JP 11 607834 607834 single base substitution G A downstream_gene_variant BTCA-JP 11 607834 607834 single base substitution G A exon_variant BTCA-JP 11 607834 607834 single base substitution G A missense_variant S789N 2366G>A BTCA-JP 11 607834 607834 single base substitution G A missense_variant S791N 2372G>A BTCA-JP 11 607834 607834 single base substitution G A missense_variant S792N 2375G>A BTCA-JP 11 607834 607834 single base substitution G A missense_variant S793N 2378G>A BTCA-JP 11 608985 608985 single base substitution C T downstream_gene_variant BTCA-JP 11 608985 608985 single base substitution C T exon_variant BTCA-JP 11 608985 608985 single base substitution C T missense_variant R1173W 3517C>T BTCA-JP 11 608985 608985 single base substitution C T missense_variant R1175W 3523C>T BTCA-JP 11 608985 608985 single base substitution C T missense_variant R1176W 3526C>T BTCA-JP 11 608985 608985 single base substitution C T missense_variant R1177W 3529C>T BTCA-JP 11 612705 612705 single base substitution G A downstream_gene_variant CESC-US 11 591399 591399 single base substitution C G exon_variant CESC-US 11 591399 591399 single base substitution C G missense_variant P142A 424C>G CESC-US 11 591399 591399 single base substitution C G missense_variant P145A 433C>G CESC-US 11 591399 591399 single base substitution C G missense_variant P146A 436C>G CESC-US 11 605255 605255 single base substitution C G exon_variant CESC-US 11 605255 605255 single base substitution C G missense_variant S426C 1277C>G CESC-US 11 605255 605255 single base substitution C G missense_variant S429C 1286C>G CESC-US 11 605255 605255 single base substitution C G missense_variant S430C 1289C>G CESC-US 11 606580 606580 single base substitution C G exon_variant CESC-US 11 606580 606580 single base substitution C G synonymous_variant L527L 1581C>G CESC-US 11 606580 606580 single base substitution C G synonymous_variant L529L 1587C>G CESC-US 11 606580 606580 single base substitution C G synonymous_variant L530L 1590C>G CESC-US 11 606580 606580 single base substitution C G synonymous_variant L531L 1593C>G CESC-US 11 607352 607352 single base substitution C T downstream_gene_variant CESC-US 11 607352 607352 single base substitution C T exon_variant CESC-US 11 607352 607352 single base substitution C T synonymous_variant F628F 1884C>T CESC-US 11 607352 607352 single base substitution C T synonymous_variant F630F 1890C>T CESC-US 11 607352 607352 single base substitution C T synonymous_variant F631F 1893C>T CESC-US 11 607352 607352 single base substitution C T synonymous_variant F632F 1896C>T CESC-US 11 608208 608208 single base substitution G C downstream_gene_variant CESC-US 11 608208 608208 single base substitution G C exon_variant CESC-US 11 608208 608208 single base substitution G C missense_variant E914Q 2740G>C CESC-US 11 608208 608208 single base substitution G C missense_variant E916Q 2746G>C CESC-US 11 608208 608208 single base substitution G C missense_variant E917Q 2749G>C CESC-US 11 608208 608208 single base substitution G C missense_variant E918Q 2752G>C CESC-US 11 608302 608302 single base substitution G A downstream_gene_variant CESC-US 11 608302 608302 single base substitution G A exon_variant CESC-US 11 608302 608302 single base substitution G A missense_variant C945Y 2834G>A CESC-US 11 608302 608302 single base substitution G A missense_variant C947Y 2840G>A CESC-US 11 608302 608302 single base substitution G A missense_variant C948Y 2843G>A CESC-US 11 608302 608302 single base substitution G A missense_variant C949Y 2846G>A CESC-US 11 610993 610993 single base substitution G A 3_prime_UTR_variant CESC-US 11 610993 610993 single base substitution G A downstream_gene_variant CESC-US 11 610993 610993 single base substitution G A missense_variant E1569K 4705G>A CESC-US 11 610993 610993 single base substitution G A missense_variant E1571K 4711G>A CESC-US 11 610993 610993 single base substitution G A missense_variant E1572K 4714G>A CESC-US 11 610993 610993 single base substitution G A missense_variant E1573K 4717G>A CESC-US 11 613210 613210 single base substitution G A downstream_gene_variant CESC-US 11 613857 613857 single base substitution C T downstream_gene_variant CESC-US 11 613863 613863 single base substitution C A downstream_gene_variant CESC-US 11 614216 614216 single base substitution C G downstream_gene_variant CLLE-ES 11 591942 591942 single base substitution G T intron_variant CLLE-ES 11 610642 610642 single base substitution C T downstream_gene_variant CLLE-ES 11 610642 610642 single base substitution C T intron_variant CLLE-ES 11 610642 610642 single base substitution C T missense_variant P1516S 4546C>T CLLE-ES 11 610642 610642 single base substitution C T missense_variant P1518S 4552C>T CLLE-ES 11 610642 610642 single base substitution C T missense_variant P1519S 4555C>T CLLE-ES 11 610642 610642 single base substitution C T missense_variant P1520S 4558C>T COAD-US 11 582025 582025 single base substitution G T exon_variant COAD-US 11 582025 582025 single base substitution G T missense_variant G49V 146G>T COAD-US 11 582025 582025 single base substitution G T missense_variant G52V 155G>T COAD-US 11 582025 582025 single base substitution G T missense_variant G53V 158G>T COAD-US 11 587278 587278 single base substitution C T exon_variant COAD-US 11 587278 587278 single base substitution C T synonymous_variant D74D 222C>T COAD-US 11 587278 587278 single base substitution C T synonymous_variant D77D 231C>T COAD-US 11 587278 587278 single base substitution C T synonymous_variant D78D 234C>T COAD-US 11 591435 591435 single base substitution C A exon_variant COAD-US 11 591435 591435 single base substitution C A synonymous_variant R154R 460C>A COAD-US 11 591435 591435 single base substitution C A synonymous_variant R157R 469C>A COAD-US 11 591435 591435 single base substitution C A synonymous_variant R158R 472C>A COAD-US 11 592566 592566 single base substitution T C exon_variant COAD-US 11 592566 592566 single base substitution T C missense_variant V167A 500T>C COAD-US 11 592566 592566 single base substitution T C missense_variant V170A 509T>C COAD-US 11 592566 592566 single base substitution T C missense_variant V171A 512T>C COAD-US 11 598459 598459 deletion of <=200bp C - exon_variant COAD-US 11 598459 598459 deletion of <=200bp C - frameshift_variant R323 COAD-US 11 598459 598459 deletion of <=200bp C - frameshift_variant R326 COAD-US 11 598459 598459 deletion of <=200bp C - frameshift_variant R327 COAD-US 11 598459 598459 deletion of <=200bp C - upstream_gene_variant COAD-US 11 601665 601665 single base substitution A G exon_variant COAD-US 11 601665 601665 single base substitution A G synonymous_variant Q368Q 1104A>G COAD-US 11 601665 601665 single base substitution A G synonymous_variant Q371Q 1113A>G COAD-US 11 601665 601665 single base substitution A G synonymous_variant Q372Q 1116A>G COAD-US 11 605170 605170 single base substitution C A exon_variant COAD-US 11 605170 605170 single base substitution C A missense_variant P398T 1192C>A COAD-US 11 605170 605170 single base substitution C A missense_variant P401T 1201C>A COAD-US 11 605170 605170 single base substitution C A missense_variant P402T 1204C>A COAD-US 11 605710 605710 single base substitution C T exon_variant COAD-US 11 605710 605710 single base substitution C T synonymous_variant S476S 1428C>T COAD-US 11 605710 605710 single base substitution C T synonymous_variant S478S 1434C>T COAD-US 11 605710 605710 single base substitution C T synonymous_variant S479S 1437C>T COAD-US 11 605710 605710 single base substitution C T synonymous_variant S480S 1440C>T COAD-US 11 605711 605711 single base substitution G A exon_variant COAD-US 11 605711 605711 single base substitution G A missense_variant V477M 1429G>A COAD-US 11 605711 605711 single base substitution G A missense_variant V479M 1435G>A COAD-US 11 605711 605711 single base substitution G A missense_variant V480M 1438G>A COAD-US 11 605711 605711 single base substitution G A missense_variant V481M 1441G>A COAD-US 11 607394 607394 single base substitution G A downstream_gene_variant COAD-US 11 607394 607394 single base substitution G A exon_variant COAD-US 11 607394 607394 single base substitution G A synonymous_variant A642A 1926G>A COAD-US 11 607394 607394 single base substitution G A synonymous_variant A644A 1932G>A COAD-US 11 607394 607394 single base substitution G A synonymous_variant A645A 1935G>A COAD-US 11 607394 607394 single base substitution G A synonymous_variant A646A 1938G>A COAD-US 11 607462 607462 single base substitution C A downstream_gene_variant COAD-US 11 607462 607462 single base substitution C A exon_variant COAD-US 11 607462 607462 single base substitution C A missense_variant P665Q 1994C>A COAD-US 11 607462 607462 single base substitution C A missense_variant P667Q 2000C>A COAD-US 11 607462 607462 single base substitution C A missense_variant P668Q 2003C>A COAD-US 11 607462 607462 single base substitution C A missense_variant P669Q 2006C>A COAD-US 11 608472 608472 single base substitution A C downstream_gene_variant COAD-US 11 608472 608472 single base substitution A C exon_variant COAD-US 11 608472 608472 single base substitution A C missense_variant K1002Q 3004A>C COAD-US 11 608472 608472 single base substitution A C missense_variant K1004Q 3010A>C COAD-US 11 608472 608472 single base substitution A C missense_variant K1005Q 3013A>C COAD-US 11 608472 608472 single base substitution A C missense_variant K1006Q 3016A>C COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - downstream_gene_variant COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - exon_variant COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1012R COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1014R COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1015R COAD-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1016R COAD-US 11 608864 608864 single base substitution G A downstream_gene_variant COAD-US 11 608864 608864 single base substitution G A exon_variant COAD-US 11 608864 608864 single base substitution G A synonymous_variant K1132K 3396G>A COAD-US 11 608864 608864 single base substitution G A synonymous_variant K1134K 3402G>A COAD-US 11 608864 608864 single base substitution G A synonymous_variant K1135K 3405G>A COAD-US 11 608864 608864 single base substitution G A synonymous_variant K1136K 3408G>A COAD-US 11 609068 609068 single base substitution G A downstream_gene_variant COAD-US 11 609068 609068 single base substitution G A exon_variant COAD-US 11 609068 609068 single base substitution G A synonymous_variant A1200A 3600G>A COAD-US 11 609068 609068 single base substitution G A synonymous_variant A1202A 3606G>A COAD-US 11 609068 609068 single base substitution G A synonymous_variant A1203A 3609G>A COAD-US 11 609068 609068 single base substitution G A synonymous_variant A1204A 3612G>A COAD-US 11 609628 609628 deletion of <=200bp C - downstream_gene_variant COAD-US 11 609628 609628 deletion of <=200bp C - exon_variant COAD-US 11 609628 609628 deletion of <=200bp C - frameshift_variant T1387 COAD-US 11 609628 609628 deletion of <=200bp C - frameshift_variant T1389 COAD-US 11 609628 609628 deletion of <=200bp C - frameshift_variant T1390 COAD-US 11 609628 609628 deletion of <=200bp C - frameshift_variant T1391 COAD-US 11 609697 609697 deletion of <=200bp C - downstream_gene_variant COAD-US 11 609697 609697 deletion of <=200bp C - exon_variant COAD-US 11 609697 609697 deletion of <=200bp C - frameshift_variant A1410 COAD-US 11 609697 609697 deletion of <=200bp C - frameshift_variant A1412 COAD-US 11 609697 609697 deletion of <=200bp C - frameshift_variant A1413 COAD-US 11 609697 609697 deletion of <=200bp C - frameshift_variant A1414 COAD-US 11 612798 612798 single base substitution C T downstream_gene_variant COAD-US 11 613285 613285 single base substitution G A downstream_gene_variant COAD-US 11 613286 613286 single base substitution G T downstream_gene_variant COAD-US 11 613300 613300 single base substitution G A downstream_gene_variant COAD-US 11 613429 613429 single base substitution C T downstream_gene_variant COAD-US 11 614864 614864 single base substitution C T downstream_gene_variant COAD-US 11 615103 615103 single base substitution G A downstream_gene_variant COCA-CN 11 582255 582255 single base substitution A T intron_variant COCA-CN 11 584999 584999 single base substitution A G intron_variant COCA-CN 11 585441 585441 single base substitution C T intron_variant COCA-CN 11 585474 585474 single base substitution T A intron_variant COCA-CN 11 585487 585487 single base substitution C T intron_variant COCA-CN 11 585589 585589 single base substitution T A intron_variant COCA-CN 11 585640 585640 single base substitution G A intron_variant COCA-CN 11 587372 587372 single base substitution A G exon_variant COCA-CN 11 587372 587372 single base substitution A G missense_variant I106V 316A>G COCA-CN 11 587372 587372 single base substitution A G missense_variant I109V 325A>G COCA-CN 11 587372 587372 single base substitution A G missense_variant I110V 328A>G COCA-CN 11 587384 587384 single base substitution G A exon_variant COCA-CN 11 587384 587384 single base substitution G A missense_variant A110T 328G>A COCA-CN 11 587384 587384 single base substitution G A missense_variant A113T 337G>A COCA-CN 11 587384 587384 single base substitution G A missense_variant A114T 340G>A COCA-CN 11 589811 589811 single base substitution A G intron_variant COCA-CN 11 589839 589839 single base substitution A T intron_variant COCA-CN 11 592597 592597 single base substitution G T exon_variant COCA-CN 11 592597 592597 single base substitution G T missense_variant E177D 531G>T COCA-CN 11 592597 592597 single base substitution G T missense_variant E180D 540G>T COCA-CN 11 592597 592597 single base substitution G T missense_variant E181D 543G>T COCA-CN 11 597045 597045 single base substitution G T intron_variant COCA-CN 11 597045 597045 single base substitution G T upstream_gene_variant COCA-CN 11 598405 598405 single base substitution G A exon_variant COCA-CN 11 598405 598405 single base substitution G A synonymous_variant L305L 915G>A COCA-CN 11 598405 598405 single base substitution G A synonymous_variant L308L 924G>A COCA-CN 11 598405 598405 single base substitution G A synonymous_variant L309L 927G>A COCA-CN 11 598405 598405 single base substitution G A upstream_gene_variant COCA-CN 11 599788 599788 single base substitution G A intron_variant COCA-CN 11 599788 599788 single base substitution G A upstream_gene_variant COCA-CN 11 599790 599790 single base substitution C T intron_variant COCA-CN 11 599790 599790 single base substitution C T upstream_gene_variant COCA-CN 11 605141 605141 single base substitution G A exon_variant COCA-CN 11 605141 605141 single base substitution G A missense_variant R388Q 1163G>A COCA-CN 11 605141 605141 single base substitution G A missense_variant R391Q 1172G>A COCA-CN 11 605141 605141 single base substitution G A missense_variant R392Q 1175G>A COCA-CN 11 605153 605153 single base substitution C T exon_variant COCA-CN 11 605153 605153 single base substitution C T missense_variant T392M 1175C>T COCA-CN 11 605153 605153 single base substitution C T missense_variant T395M 1184C>T COCA-CN 11 605153 605153 single base substitution C T missense_variant T396M 1187C>T COCA-CN 11 607106 607106 single base substitution A G downstream_gene_variant COCA-CN 11 607106 607106 single base substitution A G exon_variant COCA-CN 11 607106 607106 single base substitution A G synonymous_variant R546R 1638A>G COCA-CN 11 607106 607106 single base substitution A G synonymous_variant R548R 1644A>G COCA-CN 11 607106 607106 single base substitution A G synonymous_variant R549R 1647A>G COCA-CN 11 607106 607106 single base substitution A G synonymous_variant R550R 1650A>G COCA-CN 11 608013 608013 single base substitution G A downstream_gene_variant COCA-CN 11 608013 608013 single base substitution G A exon_variant COCA-CN 11 608013 608013 single base substitution G A missense_variant G849S 2545G>A COCA-CN 11 608013 608013 single base substitution G A missense_variant G851S 2551G>A COCA-CN 11 608013 608013 single base substitution G A missense_variant G852S 2554G>A COCA-CN 11 608013 608013 single base substitution G A missense_variant G853S 2557G>A COCA-CN 11 608578 608578 single base substitution G A downstream_gene_variant COCA-CN 11 608578 608578 single base substitution G A exon_variant COCA-CN 11 608578 608578 single base substitution G A missense_variant R1037H 3110G>A COCA-CN 11 608578 608578 single base substitution G A missense_variant R1039H 3116G>A COCA-CN 11 608578 608578 single base substitution G A missense_variant R1040H 3119G>A COCA-CN 11 608578 608578 single base substitution G A missense_variant R1041H 3122G>A COCA-CN 11 608937 608937 single base substitution C T downstream_gene_variant COCA-CN 11 608937 608937 single base substitution C T exon_variant COCA-CN 11 608937 608937 single base substitution C T missense_variant R1157W 3469C>T COCA-CN 11 608937 608937 single base substitution C T missense_variant R1159W 3475C>T COCA-CN 11 608937 608937 single base substitution C T missense_variant R1160W 3478C>T COCA-CN 11 608937 608937 single base substitution C T missense_variant R1161W 3481C>T COCA-CN 11 610142 610142 single base substitution T C downstream_gene_variant COCA-CN 11 610142 610142 single base substitution T C intron_variant COCA-CN 11 610776 610776 single base substitution C T downstream_gene_variant COCA-CN 11 610776 610776 single base substitution C T intron_variant COCA-CN 11 610958 610958 single base substitution T C 3_prime_UTR_variant COCA-CN 11 610958 610958 single base substitution T C downstream_gene_variant COCA-CN 11 610958 610958 single base substitution T C missense_variant M1557T 4670T>C COCA-CN 11 610958 610958 single base substitution T C missense_variant M1559T 4676T>C COCA-CN 11 610958 610958 single base substitution T C missense_variant M1560T 4679T>C COCA-CN 11 610958 610958 single base substitution T C missense_variant M1561T 4682T>C COCA-CN 11 611869 611869 single base substitution G A 3_prime_UTR_variant COCA-CN 11 613052 613052 single base substitution C T downstream_gene_variant COCA-CN 11 614934 614934 single base substitution G A downstream_gene_variant COCA-CN 11 615139 615139 single base substitution G A downstream_gene_variant COCA-CN 11 616815 616815 single base substitution G A downstream_gene_variant EOPC-DE 11 609760 609760 single base substitution A C downstream_gene_variant EOPC-DE 11 609760 609760 single base substitution A C intron_variant EOPC-DE 11 609819 609819 single base substitution T C downstream_gene_variant EOPC-DE 11 609819 609819 single base substitution T C intron_variant ESAD-UK 11 572292 572292 single base substitution T A upstream_gene_variant ESAD-UK 11 577782 577782 single base substitution G A intron_variant ESAD-UK 11 579253 579253 single base substitution C T intron_variant ESAD-UK 11 582706 582706 single base substitution A G intron_variant ESAD-UK 11 583434 583434 single base substitution T C intron_variant ESAD-UK 11 586511 586511 single base substitution G A intron_variant ESAD-UK 11 586638 586638 single base substitution C G intron_variant ESAD-UK 11 592635 592635 single base substitution G A exon_variant ESAD-UK 11 592635 592635 single base substitution G A missense_variant R190H 569G>A ESAD-UK 11 592635 592635 single base substitution G A missense_variant R193H 578G>A ESAD-UK 11 592635 592635 single base substitution G A missense_variant R194H 581G>A ESAD-UK 11 595271 595271 single base substitution C T intron_variant ESAD-UK 11 604741 604741 single base substitution G T intron_variant ESAD-UK 11 604944 604944 single base substitution C T intron_variant ESAD-UK 11 608248 608248 single base substitution G T downstream_gene_variant ESAD-UK 11 608248 608248 single base substitution G T exon_variant ESAD-UK 11 608248 608248 single base substitution G T missense_variant R927L 2780G>T ESAD-UK 11 608248 608248 single base substitution G T missense_variant R929L 2786G>T ESAD-UK 11 608248 608248 single base substitution G T missense_variant R930L 2789G>T ESAD-UK 11 608248 608248 single base substitution G T missense_variant R931L 2792G>T ESAD-UK 11 609171 609171 single base substitution C T downstream_gene_variant ESAD-UK 11 609171 609171 single base substitution C T exon_variant ESAD-UK 11 609171 609171 single base substitution C T missense_variant P1235S 3703C>T ESAD-UK 11 609171 609171 single base substitution C T missense_variant P1237S 3709C>T ESAD-UK 11 609171 609171 single base substitution C T missense_variant P1238S 3712C>T ESAD-UK 11 609171 609171 single base substitution C T missense_variant P1239S 3715C>T ESAD-UK 11 609200 609200 single base substitution G A downstream_gene_variant ESAD-UK 11 609200 609200 single base substitution G A exon_variant ESAD-UK 11 609200 609200 single base substitution G A synonymous_variant V1244V 3732G>A ESAD-UK 11 609200 609200 single base substitution G A synonymous_variant V1246V 3738G>A ESAD-UK 11 609200 609200 single base substitution G A synonymous_variant V1247V 3741G>A ESAD-UK 11 609200 609200 single base substitution G A synonymous_variant V1248V 3744G>A ESAD-UK 11 614890 614890 single base substitution T A downstream_gene_variant ESAD-UK 11 615423 615423 single base substitution G A downstream_gene_variant ESAD-UK 11 615898 615898 single base substitution T C downstream_gene_variant ESCA-CN 11 597432 597432 single base substitution C A exon_variant ESCA-CN 11 597432 597432 single base substitution C A synonymous_variant L248L 744C>A ESCA-CN 11 597432 597432 single base substitution C A synonymous_variant L251L 753C>A ESCA-CN 11 597432 597432 single base substitution C A synonymous_variant L252L 756C>A ESCA-CN 11 597432 597432 single base substitution C A upstream_gene_variant ESCA-CN 11 606580 606580 single base substitution C T exon_variant ESCA-CN 11 606580 606580 single base substitution C T synonymous_variant L527L 1581C>T ESCA-CN 11 606580 606580 single base substitution C T synonymous_variant L529L 1587C>T ESCA-CN 11 606580 606580 single base substitution C T synonymous_variant L530L 1590C>T ESCA-CN 11 606580 606580 single base substitution C T synonymous_variant L531L 1593C>T ESCA-CN 11 608200 608200 single base substitution C G downstream_gene_variant ESCA-CN 11 608200 608200 single base substitution C G exon_variant ESCA-CN 11 608200 608200 single base substitution C G missense_variant S911C 2732C>G ESCA-CN 11 608200 608200 single base substitution C G missense_variant S913C 2738C>G ESCA-CN 11 608200 608200 single base substitution C G missense_variant S914C 2741C>G ESCA-CN 11 608200 608200 single base substitution C G missense_variant S915C 2744C>G ESCA-CN 11 608974 608974 single base substitution G A downstream_gene_variant ESCA-CN 11 608974 608974 single base substitution G A exon_variant ESCA-CN 11 608974 608974 single base substitution G A missense_variant R1169Q 3506G>A ESCA-CN 11 608974 608974 single base substitution G A missense_variant R1171Q 3512G>A ESCA-CN 11 608974 608974 single base substitution G A missense_variant R1172Q 3515G>A ESCA-CN 11 608974 608974 single base substitution G A missense_variant R1173Q 3518G>A ESCA-CN 11 609291 609291 single base substitution G A downstream_gene_variant ESCA-CN 11 609291 609291 single base substitution G A exon_variant ESCA-CN 11 609291 609291 single base substitution G A missense_variant V1275I 3823G>A ESCA-CN 11 609291 609291 single base substitution G A missense_variant V1277I 3829G>A ESCA-CN 11 609291 609291 single base substitution G A missense_variant V1278I 3832G>A ESCA-CN 11 609291 609291 single base substitution G A missense_variant V1279I 3835G>A ESCA-CN 11 610177 610177 single base substitution C T downstream_gene_variant ESCA-CN 11 610177 610177 single base substitution C T intron_variant ESCA-CN 11 613843 613843 single base substitution G T downstream_gene_variant GBM-US 11 607162 607162 single base substitution C A downstream_gene_variant GBM-US 11 607162 607162 single base substitution C A exon_variant GBM-US 11 607162 607162 single base substitution C A missense_variant P565Q 1694C>A GBM-US 11 607162 607162 single base substitution C A missense_variant P567Q 1700C>A GBM-US 11 607162 607162 single base substitution C A missense_variant P568Q 1703C>A GBM-US 11 607162 607162 single base substitution C A missense_variant P569Q 1706C>A GBM-US 11 607393 607393 single base substitution C T downstream_gene_variant GBM-US 11 607393 607393 single base substitution C T exon_variant GBM-US 11 607393 607393 single base substitution C T missense_variant A642V 1925C>T GBM-US 11 607393 607393 single base substitution C T missense_variant A644V 1931C>T GBM-US 11 607393 607393 single base substitution C T missense_variant A645V 1934C>T GBM-US 11 607393 607393 single base substitution C T missense_variant A646V 1937C>T GBM-US 11 608268 608268 single base substitution C T downstream_gene_variant GBM-US 11 608268 608268 single base substitution C T exon_variant GBM-US 11 608268 608268 single base substitution C T missense_variant P934S 2800C>T GBM-US 11 608268 608268 single base substitution C T missense_variant P936S 2806C>T GBM-US 11 608268 608268 single base substitution C T missense_variant P937S 2809C>T GBM-US 11 608268 608268 single base substitution C T missense_variant P938S 2812C>T GBM-US 11 608380 608380 single base substitution A T downstream_gene_variant GBM-US 11 608380 608380 single base substitution A T exon_variant GBM-US 11 608380 608380 single base substitution A T missense_variant D971V 2912A>T GBM-US 11 608380 608380 single base substitution A T missense_variant D973V 2918A>T GBM-US 11 608380 608380 single base substitution A T missense_variant D974V 2921A>T GBM-US 11 608380 608380 single base substitution A T missense_variant D975V 2924A>T KIRC-US 11 608267 608267 single base substitution C A downstream_gene_variant KIRC-US 11 608267 608267 single base substitution C A exon_variant KIRC-US 11 608267 608267 single base substitution C A synonymous_variant P933P 2799C>A KIRC-US 11 608267 608267 single base substitution C A synonymous_variant P935P 2805C>A KIRC-US 11 608267 608267 single base substitution C A synonymous_variant P936P 2808C>A KIRC-US 11 608267 608267 single base substitution C A synonymous_variant P937P 2811C>A KIRC-US 11 608822 608822 single base substitution G A downstream_gene_variant KIRC-US 11 608822 608822 single base substitution G A exon_variant KIRC-US 11 608822 608822 single base substitution G A synonymous_variant E1118E 3354G>A KIRC-US 11 608822 608822 single base substitution G A synonymous_variant E1120E 3360G>A KIRC-US 11 608822 608822 single base substitution G A synonymous_variant E1121E 3363G>A KIRC-US 11 608822 608822 single base substitution G A synonymous_variant E1122E 3366G>A KIRC-US 11 611078 611078 single base substitution A C 3_prime_UTR_variant KIRC-US 11 611078 611078 single base substitution A C downstream_gene_variant KIRC-US 11 611078 611078 single base substitution A C missense_variant Q1597P 4790A>C KIRC-US 11 611078 611078 single base substitution A C missense_variant Q1599P 4796A>C KIRC-US 11 611078 611078 single base substitution A C missense_variant Q1600P 4799A>C KIRC-US 11 611078 611078 single base substitution A C missense_variant Q1601P 4802A>C KIRC-US 11 614301 614301 single base substitution G A downstream_gene_variant KIRP-US 11 601639 601639 single base substitution T C exon_variant KIRP-US 11 601639 601639 single base substitution T C missense_variant S360P 1078T>C KIRP-US 11 601639 601639 single base substitution T C missense_variant S363P 1087T>C KIRP-US 11 601639 601639 single base substitution T C missense_variant S364P 1090T>C KIRP-US 11 601639 601639 single base substitution T C upstream_gene_variant LAML-KR 11 574178 574178 single base substitution A G upstream_gene_variant LAML-KR 11 574225 574225 single base substitution G T upstream_gene_variant LAML-KR 11 581356 581356 single base substitution T A intron_variant LAML-KR 11 581629 581629 single base substitution G A intron_variant LAML-KR 11 589885 589885 single base substitution C G intron_variant LGG-US 11 592586 592588 deletion of <=200bp GAG - exon_variant LGG-US 11 592586 592588 deletion of <=200bp GAG - inframe_deletion E174 LGG-US 11 592586 592588 deletion of <=200bp GAG - inframe_deletion E177 LGG-US 11 592586 592588 deletion of <=200bp GAG - inframe_deletion E178 LGG-US 11 608555 608555 single base substitution G A downstream_gene_variant LGG-US 11 608555 608555 single base substitution G A exon_variant LGG-US 11 608555 608555 single base substitution G A synonymous_variant A1029A 3087G>A LGG-US 11 608555 608555 single base substitution G A synonymous_variant A1031A 3093G>A LGG-US 11 608555 608555 single base substitution G A synonymous_variant A1032A 3096G>A LGG-US 11 608555 608555 single base substitution G A synonymous_variant A1033A 3099G>A LICA-CN 11 587426 587426 single base substitution C A exon_variant LICA-CN 11 587426 587426 single base substitution C A missense_variant H124N 370C>A LICA-CN 11 587426 587426 single base substitution C A missense_variant H127N 379C>A LICA-CN 11 587426 587426 single base substitution C A missense_variant H128N 382C>A LICA-CN 11 607914 607914 single base substitution A T downstream_gene_variant LICA-CN 11 607914 607914 single base substitution A T exon_variant LICA-CN 11 607914 607914 single base substitution A T stop_gained K816* 2446A>T LICA-CN 11 607914 607914 single base substitution A T stop_gained K818* 2452A>T LICA-CN 11 607914 607914 single base substitution A T stop_gained K819* 2455A>T LICA-CN 11 607914 607914 single base substitution A T stop_gained K820* 2458A>T LICA-CN 11 608970 608970 single base substitution G T downstream_gene_variant LICA-CN 11 608970 608970 single base substitution G T exon_variant LICA-CN 11 608970 608970 single base substitution G T missense_variant A1168S 3502G>T LICA-CN 11 608970 608970 single base substitution G T missense_variant A1170S 3508G>T LICA-CN 11 608970 608970 single base substitution G T missense_variant A1171S 3511G>T LICA-CN 11 608970 608970 single base substitution G T missense_variant A1172S 3514G>T LICA-FR 11 582265 582266 deletion of <=200bp TT - intron_variant LICA-FR 11 585543 585543 single base substitution T A intron_variant LICA-FR 11 585556 585556 single base substitution C T intron_variant LICA-FR 11 585773 585773 single base substitution C A intron_variant LICA-FR 11 588787 588787 single base substitution A G intron_variant LICA-FR 11 605169 605169 single base substitution G T exon_variant LICA-FR 11 605169 605169 single base substitution G T missense_variant R397S 1191G>T LICA-FR 11 605169 605169 single base substitution G T missense_variant R400S 1200G>T LICA-FR 11 605169 605169 single base substitution G T missense_variant R401S 1203G>T LICA-FR 11 606595 606595 single base substitution G T exon_variant LICA-FR 11 606595 606595 single base substitution G T splice_region_variant LICA-FR 11 607688 607688 single base substitution C T downstream_gene_variant LICA-FR 11 607688 607688 single base substitution C T exon_variant LICA-FR 11 607688 607688 single base substitution C T synonymous_variant H740H 2220C>T LICA-FR 11 607688 607688 single base substitution C T synonymous_variant H742H 2226C>T LICA-FR 11 607688 607688 single base substitution C T synonymous_variant H743H 2229C>T LICA-FR 11 607688 607688 single base substitution C T synonymous_variant H744H 2232C>T LICA-FR 11 609109 609109 single base substitution C G downstream_gene_variant LICA-FR 11 609109 609109 single base substitution C G exon_variant LICA-FR 11 609109 609109 single base substitution C G missense_variant T1214S 3641C>G LICA-FR 11 609109 609109 single base substitution C G missense_variant T1216S 3647C>G LICA-FR 11 609109 609109 single base substitution C G missense_variant T1217S 3650C>G LICA-FR 11 609109 609109 single base substitution C G missense_variant T1218S 3653C>G LICA-FR 11 615265 615265 single base substitution G T downstream_gene_variant LIHC-US 11 587380 587380 single base substitution C A exon_variant LIHC-US 11 587380 587380 single base substitution C A synonymous_variant L108L 324C>A LIHC-US 11 587380 587380 single base substitution C A synonymous_variant L111L 333C>A LIHC-US 11 587380 587380 single base substitution C A synonymous_variant L112L 336C>A LIHC-US 11 592654 592654 single base substitution C G exon_variant LIHC-US 11 592654 592654 single base substitution C G synonymous_variant L196L 588C>G LIHC-US 11 592654 592654 single base substitution C G synonymous_variant L199L 597C>G LIHC-US 11 592654 592654 single base substitution C G synonymous_variant L200L 600C>G LIHC-US 11 606503 606503 single base substitution C T exon_variant LIHC-US 11 606503 606503 single base substitution C T synonymous_variant L502L 1504C>T LIHC-US 11 606503 606503 single base substitution C T synonymous_variant L504L 1510C>T LIHC-US 11 606503 606503 single base substitution C T synonymous_variant L505L 1513C>T LIHC-US 11 606503 606503 single base substitution C T synonymous_variant L506L 1516C>T LIHC-US 11 608299 608299 single base substitution C T downstream_gene_variant LIHC-US 11 608299 608299 single base substitution C T exon_variant LIHC-US 11 608299 608299 single base substitution C T missense_variant S944F 2831C>T LIHC-US 11 608299 608299 single base substitution C T missense_variant S946F 2837C>T LIHC-US 11 608299 608299 single base substitution C T missense_variant S947F 2840C>T LIHC-US 11 608299 608299 single base substitution C T missense_variant S948F 2843C>T LIHC-US 11 608998 608998 single base substitution G T downstream_gene_variant LIHC-US 11 608998 608998 single base substitution G T exon_variant LIHC-US 11 608998 608998 single base substitution G T missense_variant R1177L 3530G>T LIHC-US 11 608998 608998 single base substitution G T missense_variant R1179L 3536G>T LIHC-US 11 608998 608998 single base substitution G T missense_variant R1180L 3539G>T LIHC-US 11 608998 608998 single base substitution G T missense_variant R1181L 3542G>T LIHC-US 11 609135 609135 single base substitution C G downstream_gene_variant LIHC-US 11 609135 609135 single base substitution C G exon_variant LIHC-US 11 609135 609135 single base substitution C G missense_variant H1223D 3667C>G LIHC-US 11 609135 609135 single base substitution C G missense_variant H1225D 3673C>G LIHC-US 11 609135 609135 single base substitution C G missense_variant H1226D 3676C>G LIHC-US 11 609135 609135 single base substitution C G missense_variant H1227D 3679C>G LIHC-US 11 609443 609443 single base substitution A G downstream_gene_variant LIHC-US 11 609443 609443 single base substitution A G exon_variant LIHC-US 11 609443 609443 single base substitution A G synonymous_variant E1325E 3975A>G LIHC-US 11 609443 609443 single base substitution A G synonymous_variant E1327E 3981A>G LIHC-US 11 609443 609443 single base substitution A G synonymous_variant E1328E 3984A>G LIHC-US 11 609443 609443 single base substitution A G synonymous_variant E1329E 3987A>G LIHC-US 11 610529 610529 single base substitution C T downstream_gene_variant LIHC-US 11 610529 610529 single base substitution C T intron_variant LIHC-US 11 610529 610529 single base substitution C T missense_variant P1478L 4433C>T LIHC-US 11 610529 610529 single base substitution C T missense_variant P1480L 4439C>T LIHC-US 11 610529 610529 single base substitution C T missense_variant P1481L 4442C>T LIHC-US 11 610529 610529 single base substitution C T missense_variant P1482L 4445C>T LIHC-US 11 611702 611702 single base substitution C A 3_prime_UTR_variant LIHC-US 11 611702 611702 single base substitution C A downstream_gene_variant LIHC-US 11 611702 611702 single base substitution C A missense_variant D1621E 4863C>A LIHC-US 11 611702 611702 single base substitution C A missense_variant D1623E 4869C>A LIHC-US 11 611702 611702 single base substitution C A missense_variant D1624E 4872C>A LIHC-US 11 611702 611702 single base substitution C A missense_variant D1625E 4875C>A LIHC-US 11 611703 611703 single base substitution A G 3_prime_UTR_variant LIHC-US 11 611703 611703 single base substitution A G downstream_gene_variant LIHC-US 11 611703 611703 single base substitution A G missense_variant K1622E 4864A>G LIHC-US 11 611703 611703 single base substitution A G missense_variant K1624E 4870A>G LIHC-US 11 611703 611703 single base substitution A G missense_variant K1625E 4873A>G LIHC-US 11 611703 611703 single base substitution A G missense_variant K1626E 4876A>G LINC-JP 11 582281 582281 single base substitution T G intron_variant LINC-JP 11 591485 591485 single base substitution C T intron_variant LINC-JP 11 592596 592596 single base substitution A G exon_variant LINC-JP 11 592596 592596 single base substitution A G missense_variant E177G 530A>G LINC-JP 11 592596 592596 single base substitution A G missense_variant E180G 539A>G LINC-JP 11 592596 592596 single base substitution A G missense_variant E181G 542A>G LINC-JP 11 595536 595536 single base substitution C G intron_variant LINC-JP 11 596964 596964 single base substitution C T exon_variant LINC-JP 11 596964 596964 single base substitution C T missense_variant P217L 650C>T LINC-JP 11 596964 596964 single base substitution C T missense_variant P220L 659C>T LINC-JP 11 596964 596964 single base substitution C T missense_variant P221L 662C>T LINC-JP 11 596964 596964 single base substitution C T upstream_gene_variant LINC-JP 11 597005 597005 single base substitution G T exon_variant LINC-JP 11 597005 597005 single base substitution G T missense_variant V231F 691G>T LINC-JP 11 597005 597005 single base substitution G T missense_variant V234F 700G>T LINC-JP 11 597005 597005 single base substitution G T missense_variant V235F 703G>T LINC-JP 11 597005 597005 single base substitution G T upstream_gene_variant LINC-JP 11 597008 597008 single base substitution G T exon_variant LINC-JP 11 597008 597008 single base substitution G T missense_variant V232F 694G>T LINC-JP 11 597008 597008 single base substitution G T missense_variant V235F 703G>T LINC-JP 11 597008 597008 single base substitution G T missense_variant V236F 706G>T LINC-JP 11 597008 597008 single base substitution G T upstream_gene_variant LINC-JP 11 605549 605549 single base substitution G C intron_variant LINC-JP 11 609053 609053 single base substitution G T downstream_gene_variant LINC-JP 11 609053 609053 single base substitution G T exon_variant LINC-JP 11 609053 609053 single base substitution G T missense_variant R1195S 3585G>T LINC-JP 11 609053 609053 single base substitution G T missense_variant R1197S 3591G>T LINC-JP 11 609053 609053 single base substitution G T missense_variant R1198S 3594G>T LINC-JP 11 609053 609053 single base substitution G T missense_variant R1199S 3597G>T LINC-JP 11 609361 609361 single base substitution A G downstream_gene_variant LINC-JP 11 609361 609361 single base substitution A G exon_variant LINC-JP 11 609361 609361 single base substitution A G missense_variant D1298G 3893A>G LINC-JP 11 609361 609361 single base substitution A G missense_variant D1300G 3899A>G LINC-JP 11 609361 609361 single base substitution A G missense_variant D1301G 3902A>G LINC-JP 11 609361 609361 single base substitution A G missense_variant D1302G 3905A>G LINC-JP 11 609848 609848 single base substitution G A downstream_gene_variant LINC-JP 11 609848 609848 single base substitution G A intron_variant LINC-JP 11 610292 610292 single base substitution C T downstream_gene_variant LINC-JP 11 610292 610292 single base substitution C T exon_variant LINC-JP 11 610292 610292 single base substitution C T missense_variant P1450L 4349C>T LINC-JP 11 610292 610292 single base substitution C T missense_variant P1452L 4355C>T LINC-JP 11 610292 610292 single base substitution C T missense_variant P1453L 4358C>T LINC-JP 11 610292 610292 single base substitution C T missense_variant P1454L 4361C>T LINC-JP 11 610493 610493 single base substitution C T downstream_gene_variant LINC-JP 11 610493 610493 single base substitution C T intron_variant LINC-JP 11 610493 610493 single base substitution C T splice_region_variant LINC-JP 11 611145 611145 single base substitution C G downstream_gene_variant LINC-JP 11 611145 611145 single base substitution C G intron_variant LINC-JP 11 611618 611654 deletion of <=200bp GCACCTCTTTCTCCAGATCTGCCACAGCAAGAGTGGA - downstream_gene_variant LINC-JP 11 611618 611654 deletion of <=200bp GCACCTCTTTCTCCAGATCTGCCACAGCAAGAGTGGA - splice_acceptor_variant LINC-JP 11 613042 613042 single base substitution A G downstream_gene_variant LINC-JP 11 616860 616860 single base substitution G A downstream_gene_variant LINC-JP 11 617080 617080 single base substitution G A downstream_gene_variant LIRI-JP 11 572098 572098 single base substitution T C upstream_gene_variant LIRI-JP 11 577995 577995 single base substitution A T intron_variant LIRI-JP 11 579800 579800 single base substitution T G intron_variant LIRI-JP 11 579812 579812 single base substitution G A intron_variant LIRI-JP 11 581957 581957 single base substitution T G splice_region_variant LIRI-JP 11 583925 583925 single base substitution T C intron_variant LIRI-JP 11 584111 584111 single base substitution C T intron_variant LIRI-JP 11 586350 586350 single base substitution C T intron_variant LIRI-JP 11 586618 586618 single base substitution T C intron_variant LIRI-JP 11 586941 586941 single base substitution G A intron_variant LIRI-JP 11 587598 587598 single base substitution A G intron_variant LIRI-JP 11 589639 589642 deletion of <=200bp CGGA - intron_variant LIRI-JP 11 591745 591745 single base substitution G T intron_variant LIRI-JP 11 593107 593107 single base substitution C T intron_variant LIRI-JP 11 593532 593532 single base substitution C T intron_variant LIRI-JP 11 594024 594024 single base substitution G T intron_variant LIRI-JP 11 595330 595330 single base substitution G A intron_variant LIRI-JP 11 596815 596815 single base substitution C T intron_variant LIRI-JP 11 596815 596815 single base substitution C T upstream_gene_variant LIRI-JP 11 598621 598621 single base substitution T A intron_variant LIRI-JP 11 598621 598621 single base substitution T A upstream_gene_variant LIRI-JP 11 599143 599143 single base substitution A G intron_variant LIRI-JP 11 599143 599143 single base substitution A G upstream_gene_variant LIRI-JP 11 599658 599658 single base substitution A T intron_variant LIRI-JP 11 599658 599658 single base substitution A T upstream_gene_variant LIRI-JP 11 603659 603659 single base substitution G C intron_variant LIRI-JP 11 607116 607116 single base substitution G T downstream_gene_variant LIRI-JP 11 607116 607116 single base substitution G T exon_variant LIRI-JP 11 607116 607116 single base substitution G T stop_gained G550* 1648G>T LIRI-JP 11 607116 607116 single base substitution G T stop_gained G552* 1654G>T LIRI-JP 11 607116 607116 single base substitution G T stop_gained G553* 1657G>T LIRI-JP 11 607116 607116 single base substitution G T stop_gained G554* 1660G>T LIRI-JP 11 608811 608811 single base substitution C T downstream_gene_variant LIRI-JP 11 608811 608811 single base substitution C T exon_variant LIRI-JP 11 608811 608811 single base substitution C T missense_variant R1115W 3343C>T LIRI-JP 11 608811 608811 single base substitution C T missense_variant R1117W 3349C>T LIRI-JP 11 608811 608811 single base substitution C T missense_variant R1118W 3352C>T LIRI-JP 11 608811 608811 single base substitution C T missense_variant R1119W 3355C>T LIRI-JP 11 611107 611107 single base substitution T G downstream_gene_variant LIRI-JP 11 611107 611107 single base substitution T G intron_variant LIRI-JP 11 614374 614374 single base substitution G T downstream_gene_variant LUSC-KR 11 573577 573577 single base substitution C G upstream_gene_variant LUSC-KR 11 573995 573995 single base substitution C G upstream_gene_variant LUSC-KR 11 574178 574178 single base substitution A G upstream_gene_variant LUSC-KR 11 574225 574225 single base substitution G T upstream_gene_variant LUSC-KR 11 576760 576760 single base substitution C G intron_variant LUSC-KR 11 578890 578890 single base substitution C T intron_variant LUSC-KR 11 580936 580936 single base substitution G C intron_variant LUSC-KR 11 582593 582593 single base substitution C T intron_variant LUSC-KR 11 585395 585395 single base substitution C T intron_variant LUSC-KR 11 585635 585635 single base substitution T A intron_variant LUSC-KR 11 589855 589855 single base substitution C T intron_variant LUSC-KR 11 593297 593297 single base substitution G C intron_variant LUSC-KR 11 600317 600317 single base substitution A T intron_variant LUSC-KR 11 600317 600317 single base substitution A T upstream_gene_variant LUSC-KR 11 601392 601392 single base substitution G T intron_variant LUSC-KR 11 601392 601392 single base substitution G T upstream_gene_variant LUSC-KR 11 601805 601805 single base substitution G T intron_variant LUSC-KR 11 609270 609270 single base substitution G C downstream_gene_variant LUSC-KR 11 609270 609270 single base substitution G C exon_variant LUSC-KR 11 609270 609270 single base substitution G C missense_variant D1268H 3802G>C LUSC-KR 11 609270 609270 single base substitution G C missense_variant D1270H 3808G>C LUSC-KR 11 609270 609270 single base substitution G C missense_variant D1271H 3811G>C LUSC-KR 11 609270 609270 single base substitution G C missense_variant D1272H 3814G>C LUSC-KR 11 609564 609564 single base substitution G T downstream_gene_variant LUSC-KR 11 609564 609564 single base substitution G T exon_variant LUSC-KR 11 609564 609564 single base substitution G T missense_variant D1366Y 4096G>T LUSC-KR 11 609564 609564 single base substitution G T missense_variant D1368Y 4102G>T LUSC-KR 11 609564 609564 single base substitution G T missense_variant D1369Y 4105G>T LUSC-KR 11 609564 609564 single base substitution G T missense_variant D1370Y 4108G>T LUSC-US 11 601622 601622 single base substitution C G exon_variant LUSC-US 11 601622 601622 single base substitution C G missense_variant S354C 1061C>G LUSC-US 11 601622 601622 single base substitution C G missense_variant S357C 1070C>G LUSC-US 11 601622 601622 single base substitution C G missense_variant S358C 1073C>G LUSC-US 11 601622 601622 single base substitution C G upstream_gene_variant LUSC-US 11 607998 607998 single base substitution G A downstream_gene_variant LUSC-US 11 607998 607998 single base substitution G A exon_variant LUSC-US 11 607998 607998 single base substitution G A missense_variant E844K 2530G>A LUSC-US 11 607998 607998 single base substitution G A missense_variant E846K 2536G>A LUSC-US 11 607998 607998 single base substitution G A missense_variant E847K 2539G>A LUSC-US 11 607998 607998 single base substitution G A missense_variant E848K 2542G>A LUSC-US 11 608235 608235 single base substitution G T downstream_gene_variant LUSC-US 11 608235 608235 single base substitution G T exon_variant LUSC-US 11 608235 608235 single base substitution G T missense_variant G923C 2767G>T LUSC-US 11 608235 608235 single base substitution G T missense_variant G925C 2773G>T LUSC-US 11 608235 608235 single base substitution G T missense_variant G926C 2776G>T LUSC-US 11 608235 608235 single base substitution G T missense_variant G927C 2779G>T LUSC-US 11 608509 608509 single base substitution G T downstream_gene_variant LUSC-US 11 608509 608509 single base substitution G T exon_variant LUSC-US 11 608509 608509 single base substitution G T missense_variant R1014L 3041G>T LUSC-US 11 608509 608509 single base substitution G T missense_variant R1016L 3047G>T LUSC-US 11 608509 608509 single base substitution G T missense_variant R1017L 3050G>T LUSC-US 11 608509 608509 single base substitution G T missense_variant R1018L 3053G>T LUSC-US 11 608828 608828 single base substitution C T downstream_gene_variant LUSC-US 11 608828 608828 single base substitution C T exon_variant LUSC-US 11 608828 608828 single base substitution C T synonymous_variant S1120S 3360C>T LUSC-US 11 608828 608828 single base substitution C T synonymous_variant S1122S 3366C>T LUSC-US 11 608828 608828 single base substitution C T synonymous_variant S1123S 3369C>T LUSC-US 11 608828 608828 single base substitution C T synonymous_variant S1124S 3372C>T LUSC-US 11 611692 611692 single base substitution C G 3_prime_UTR_variant LUSC-US 11 611692 611692 single base substitution C G downstream_gene_variant LUSC-US 11 611692 611692 single base substitution C G missense_variant A1618G 4853C>G LUSC-US 11 611692 611692 single base substitution C G missense_variant A1620G 4859C>G LUSC-US 11 611692 611692 single base substitution C G missense_variant A1621G 4862C>G LUSC-US 11 611692 611692 single base substitution C G missense_variant A1622G 4865C>G LUSC-US 11 612717 612717 single base substitution G A downstream_gene_variant MALY-DE 11 572776 572776 single base substitution G T upstream_gene_variant MALY-DE 11 577046 577046 single base substitution C T intron_variant MALY-DE 11 582484 582484 single base substitution C G intron_variant MALY-DE 11 583432 583432 single base substitution G A intron_variant MALY-DE 11 594323 594323 single base substitution G A intron_variant MALY-DE 11 597616 597616 single base substitution A G intron_variant MALY-DE 11 597616 597616 single base substitution A G upstream_gene_variant MALY-DE 11 601802 601802 single base substitution C T intron_variant MALY-DE 11 610573 610573 single base substitution C T downstream_gene_variant MALY-DE 11 610573 610573 single base substitution C T intron_variant MALY-DE 11 610573 610573 single base substitution C T missense_variant P1493S 4477C>T MALY-DE 11 610573 610573 single base substitution C T missense_variant P1495S 4483C>T MALY-DE 11 610573 610573 single base substitution C T missense_variant P1496S 4486C>T MALY-DE 11 610573 610573 single base substitution C T missense_variant P1497S 4489C>T MELA-AU 11 572768 572768 single base substitution G A upstream_gene_variant MELA-AU 11 572806 572806 single base substitution A G upstream_gene_variant MELA-AU 11 574165 574165 single base substitution G A upstream_gene_variant MELA-AU 11 576157 576157 single base substitution G A upstream_gene_variant MELA-AU 11 577223 577223 single base substitution T C intron_variant MELA-AU 11 577916 577916 single base substitution C T intron_variant MELA-AU 11 578303 578303 single base substitution A G intron_variant MELA-AU 11 578457 578457 single base substitution C A intron_variant MELA-AU 11 579571 579571 single base substitution G T intron_variant MELA-AU 11 581023 581023 single base substitution C T intron_variant MELA-AU 11 581665 581665 single base substitution C T intron_variant MELA-AU 11 583006 583006 single base substitution C T intron_variant MELA-AU 11 583262 583262 single base substitution C T intron_variant MELA-AU 11 583305 583305 single base substitution C T intron_variant MELA-AU 11 584216 584216 single base substitution G A intron_variant MELA-AU 11 585006 585006 single base substitution G T intron_variant MELA-AU 11 585184 585184 single base substitution C T intron_variant MELA-AU 11 585262 585262 single base substitution C T intron_variant MELA-AU 11 586510 586510 single base substitution C T intron_variant MELA-AU 11 588077 588077 single base substitution C T intron_variant MELA-AU 11 588103 588103 single base substitution C T intron_variant MELA-AU 11 588203 588203 single base substitution T C intron_variant MELA-AU 11 589105 589105 single base substitution C T intron_variant MELA-AU 11 589543 589543 single base substitution T A intron_variant MELA-AU 11 589558 589558 single base substitution G A intron_variant MELA-AU 11 589644 589644 single base substitution G A intron_variant MELA-AU 11 589657 589657 single base substitution C T intron_variant MELA-AU 11 590259 590259 single base substitution C T intron_variant MELA-AU 11 590694 590694 single base substitution C T intron_variant MELA-AU 11 591215 591215 single base substitution G A intron_variant MELA-AU 11 591394 591394 single base substitution C T exon_variant MELA-AU 11 591394 591394 single base substitution C T missense_variant S140F 419C>T MELA-AU 11 591394 591394 single base substitution C T missense_variant S143F 428C>T MELA-AU 11 591394 591394 single base substitution C T missense_variant S144F 431C>T MELA-AU 11 591544 591544 single base substitution G A intron_variant MELA-AU 11 591622 591622 single base substitution C T intron_variant MELA-AU 11 592292 592292 single base substitution C T intron_variant MELA-AU 11 592327 592327 single base substitution C T intron_variant MELA-AU 11 592555 592555 single base substitution C T splice_region_variant MELA-AU 11 592673 592673 single base substitution G A missense_variant G203R 607G>A MELA-AU 11 592673 592673 single base substitution G A missense_variant G206R 616G>A MELA-AU 11 592673 592673 single base substitution G A missense_variant G207R 619G>A MELA-AU 11 592673 592673 single base substitution G A splice_region_variant MELA-AU 11 593000 593001 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 593150 593150 single base substitution C T intron_variant MELA-AU 11 593297 593297 single base substitution G A intron_variant MELA-AU 11 593317 593317 single base substitution C T intron_variant MELA-AU 11 593762 593762 single base substitution C T intron_variant MELA-AU 11 593878 593878 single base substitution C T intron_variant MELA-AU 11 594021 594021 single base substitution C T intron_variant MELA-AU 11 594399 594399 single base substitution C T intron_variant MELA-AU 11 594483 594483 single base substitution C T intron_variant MELA-AU 11 595059 595059 single base substitution C T intron_variant MELA-AU 11 595291 595292 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 595909 595909 single base substitution C T intron_variant MELA-AU 11 596293 596294 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 596584 596584 single base substitution C T intron_variant MELA-AU 11 596642 596643 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 596704 596704 single base substitution G A intron_variant MELA-AU 11 596704 596704 single base substitution G A upstream_gene_variant MELA-AU 11 597426 597426 single base substitution C T exon_variant MELA-AU 11 597426 597426 single base substitution C T synonymous_variant S246S 738C>T MELA-AU 11 597426 597426 single base substitution C T synonymous_variant S249S 747C>T MELA-AU 11 597426 597426 single base substitution C T synonymous_variant S250S 750C>T MELA-AU 11 597426 597426 single base substitution C T upstream_gene_variant MELA-AU 11 597839 597840 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 11 597839 597840 multiple base substitution (>=2bp and <=200bp) CC GT upstream_gene_variant MELA-AU 11 597841 597841 single base substitution C T intron_variant MELA-AU 11 597841 597841 single base substitution C T upstream_gene_variant MELA-AU 11 597854 597854 single base substitution C T intron_variant MELA-AU 11 597854 597854 single base substitution C T upstream_gene_variant MELA-AU 11 597873 597873 single base substitution C T intron_variant MELA-AU 11 597873 597873 single base substitution C T upstream_gene_variant MELA-AU 11 599234 599234 single base substitution T A intron_variant MELA-AU 11 599234 599234 single base substitution T A upstream_gene_variant MELA-AU 11 599449 599449 single base substitution C T intron_variant MELA-AU 11 599449 599449 single base substitution C T upstream_gene_variant MELA-AU 11 601144 601144 single base substitution C T intron_variant MELA-AU 11 601144 601144 single base substitution C T upstream_gene_variant MELA-AU 11 601204 601204 single base substitution G A intron_variant MELA-AU 11 601204 601204 single base substitution G A upstream_gene_variant MELA-AU 11 601568 601568 single base substitution C T splice_region_variant MELA-AU 11 601568 601568 single base substitution C T upstream_gene_variant MELA-AU 11 601782 601782 single base substitution C T intron_variant MELA-AU 11 602996 602996 single base substitution C T intron_variant MELA-AU 11 603121 603121 single base substitution C T intron_variant MELA-AU 11 603146 603146 single base substitution C T intron_variant MELA-AU 11 603991 603991 single base substitution C T intron_variant MELA-AU 11 604180 604180 single base substitution G A intron_variant MELA-AU 11 604413 604413 single base substitution G A intron_variant MELA-AU 11 605451 605451 single base substitution T C intron_variant MELA-AU 11 605529 605529 single base substitution C T intron_variant MELA-AU 11 606060 606060 single base substitution G T intron_variant MELA-AU 11 606246 606253 deletion of <=200bp CTCCCTCC - intron_variant MELA-AU 11 607075 607075 single base substitution C T downstream_gene_variant MELA-AU 11 607075 607075 single base substitution C T exon_variant MELA-AU 11 607075 607075 single base substitution C T missense_variant S536F 1607C>T MELA-AU 11 607075 607075 single base substitution C T missense_variant S538F 1613C>T MELA-AU 11 607075 607075 single base substitution C T missense_variant S539F 1616C>T MELA-AU 11 607075 607075 single base substitution C T missense_variant S540F 1619C>T MELA-AU 11 607306 607306 single base substitution C T downstream_gene_variant MELA-AU 11 607306 607306 single base substitution C T exon_variant MELA-AU 11 607306 607306 single base substitution C T missense_variant S613L 1838C>T MELA-AU 11 607306 607306 single base substitution C T missense_variant S615L 1844C>T MELA-AU 11 607306 607306 single base substitution C T missense_variant S616L 1847C>T MELA-AU 11 607306 607306 single base substitution C T missense_variant S617L 1850C>T MELA-AU 11 607313 607313 single base substitution G A downstream_gene_variant MELA-AU 11 607313 607313 single base substitution G A exon_variant MELA-AU 11 607313 607313 single base substitution G A synonymous_variant G615G 1845G>A MELA-AU 11 607313 607313 single base substitution G A synonymous_variant G617G 1851G>A MELA-AU 11 607313 607313 single base substitution G A synonymous_variant G618G 1854G>A MELA-AU 11 607313 607313 single base substitution G A synonymous_variant G619G 1857G>A MELA-AU 11 607722 607722 single base substitution C T downstream_gene_variant MELA-AU 11 607722 607722 single base substitution C T exon_variant MELA-AU 11 607722 607722 single base substitution C T missense_variant H752Y 2254C>T MELA-AU 11 607722 607722 single base substitution C T missense_variant H754Y 2260C>T MELA-AU 11 607722 607722 single base substitution C T missense_variant H755Y 2263C>T MELA-AU 11 607722 607722 single base substitution C T missense_variant H756Y 2266C>T MELA-AU 11 608932 608932 single base substitution G A downstream_gene_variant MELA-AU 11 608932 608932 single base substitution G A exon_variant MELA-AU 11 608932 608932 single base substitution G A missense_variant R1155K 3464G>A MELA-AU 11 608932 608932 single base substitution G A missense_variant R1157K 3470G>A MELA-AU 11 608932 608932 single base substitution G A missense_variant R1158K 3473G>A MELA-AU 11 608932 608932 single base substitution G A missense_variant R1159K 3476G>A MELA-AU 11 609603 609603 single base substitution C T downstream_gene_variant MELA-AU 11 609603 609603 single base substitution C T exon_variant MELA-AU 11 609603 609603 single base substitution C T missense_variant R1379W 4135C>T MELA-AU 11 609603 609603 single base substitution C T missense_variant R1381W 4141C>T MELA-AU 11 609603 609603 single base substitution C T missense_variant R1382W 4144C>T MELA-AU 11 609603 609603 single base substitution C T missense_variant R1383W 4147C>T MELA-AU 11 609798 609798 single base substitution C T downstream_gene_variant MELA-AU 11 609798 609798 single base substitution C T intron_variant MELA-AU 11 609814 609814 single base substitution C T downstream_gene_variant MELA-AU 11 609814 609814 single base substitution C T intron_variant MELA-AU 11 609837 609837 single base substitution C T downstream_gene_variant MELA-AU 11 609837 609837 single base substitution C T intron_variant MELA-AU 11 609893 609893 single base substitution C T downstream_gene_variant MELA-AU 11 609893 609893 single base substitution C T intron_variant MELA-AU 11 610548 610548 single base substitution C T downstream_gene_variant MELA-AU 11 610548 610548 single base substitution C T intron_variant MELA-AU 11 610548 610548 single base substitution C T synonymous_variant I1484I 4452C>T MELA-AU 11 610548 610548 single base substitution C T synonymous_variant I1486I 4458C>T MELA-AU 11 610548 610548 single base substitution C T synonymous_variant I1487I 4461C>T MELA-AU 11 610548 610548 single base substitution C T synonymous_variant I1488I 4464C>T MELA-AU 11 610603 610603 single base substitution C T downstream_gene_variant MELA-AU 11 610603 610603 single base substitution C T intron_variant MELA-AU 11 610603 610603 single base substitution C T synonymous_variant L1503L 4507C>T MELA-AU 11 610603 610603 single base substitution C T synonymous_variant L1505L 4513C>T MELA-AU 11 610603 610603 single base substitution C T synonymous_variant L1506L 4516C>T MELA-AU 11 610603 610603 single base substitution C T synonymous_variant L1507L 4519C>T MELA-AU 11 612126 612126 single base substitution T C 3_prime_UTR_variant MELA-AU 11 612126 612126 single base substitution T C downstream_gene_variant MELA-AU 11 612281 612281 single base substitution G A downstream_gene_variant MELA-AU 11 612317 612317 single base substitution G A downstream_gene_variant MELA-AU 11 612745 612745 single base substitution G A downstream_gene_variant MELA-AU 11 615225 615226 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 615894 615895 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 615945 615945 single base substitution C T downstream_gene_variant MELA-AU 11 616526 616526 single base substitution C T downstream_gene_variant ORCA-IN 11 581157 581157 single base substitution G A intron_variant ORCA-IN 11 587225 587225 single base substitution C G intron_variant ORCA-IN 11 601682 601682 single base substitution G T exon_variant ORCA-IN 11 601682 601682 single base substitution G T missense_variant R374I 1121G>T ORCA-IN 11 601682 601682 single base substitution G T missense_variant R377I 1130G>T ORCA-IN 11 601682 601682 single base substitution G T missense_variant R378I 1133G>T ORCA-IN 11 609346 609346 single base substitution C T downstream_gene_variant ORCA-IN 11 609346 609346 single base substitution C T exon_variant ORCA-IN 11 609346 609346 single base substitution C T missense_variant S1293F 3878C>T ORCA-IN 11 609346 609346 single base substitution C T missense_variant S1295F 3884C>T ORCA-IN 11 609346 609346 single base substitution C T missense_variant S1296F 3887C>T ORCA-IN 11 609346 609346 single base substitution C T missense_variant S1297F 3890C>T OV-AU 11 575527 575527 single base substitution G T upstream_gene_variant OV-AU 11 584130 584130 single base substitution A T intron_variant OV-AU 11 586260 586260 single base substitution C T intron_variant OV-AU 11 594004 594004 single base substitution C G intron_variant OV-AU 11 598305 598305 single base substitution A T intron_variant OV-AU 11 598305 598305 single base substitution A T upstream_gene_variant OV-AU 11 598390 598390 single base substitution C T exon_variant OV-AU 11 598390 598390 single base substitution C T synonymous_variant L300L 900C>T OV-AU 11 598390 598390 single base substitution C T synonymous_variant L303L 909C>T OV-AU 11 598390 598390 single base substitution C T synonymous_variant L304L 912C>T OV-AU 11 598390 598390 single base substitution C T upstream_gene_variant OV-AU 11 602565 602565 single base substitution C T intron_variant OV-AU 11 602831 602831 single base substitution C T intron_variant OV-AU 11 607372 607372 single base substitution C A downstream_gene_variant OV-AU 11 607372 607372 single base substitution C A exon_variant OV-AU 11 607372 607372 single base substitution C A missense_variant T635N 1904C>A OV-AU 11 607372 607372 single base substitution C A missense_variant T637N 1910C>A OV-AU 11 607372 607372 single base substitution C A missense_variant T638N 1913C>A OV-AU 11 607372 607372 single base substitution C A missense_variant T639N 1916C>A OV-AU 11 614905 614905 single base substitution G A downstream_gene_variant PACA-AU 11 577856 577856 single base substitution C T intron_variant PACA-AU 11 578303 578303 single base substitution A G intron_variant PACA-AU 11 578349 578349 single base substitution G A intron_variant PACA-AU 11 584145 584145 single base substitution C T intron_variant PACA-AU 11 588389 588389 single base substitution G T intron_variant PACA-AU 11 593161 593161 single base substitution G C intron_variant PACA-AU 11 594820 594822 deletion of <=200bp TTA - intron_variant PACA-AU 11 598247 598247 single base substitution C T intron_variant PACA-AU 11 598247 598247 single base substitution C T upstream_gene_variant PACA-AU 11 599604 599604 single base substitution C T intron_variant PACA-AU 11 599604 599604 single base substitution C T upstream_gene_variant PACA-AU 11 599915 599915 single base substitution T A intron_variant PACA-AU 11 599915 599915 single base substitution T A upstream_gene_variant PACA-AU 11 603681 603681 single base substitution A T intron_variant PACA-AU 11 604707 604707 single base substitution G C intron_variant PACA-AU 11 613470 613470 single base substitution C A downstream_gene_variant PACA-AU 11 616089 616089 single base substitution C T downstream_gene_variant PACA-AU 11 616721 616721 single base substitution T C downstream_gene_variant PACA-CA 11 571593 571593 single base substitution G T upstream_gene_variant PACA-CA 11 571870 571870 single base substitution G A upstream_gene_variant PACA-CA 11 572527 572527 single base substitution T G upstream_gene_variant PACA-CA 11 583357 583357 single base substitution C A intron_variant PACA-CA 11 584637 584637 single base substitution G C intron_variant PACA-CA 11 586041 586041 single base substitution T A intron_variant PACA-CA 11 588283 588283 single base substitution C T intron_variant PACA-CA 11 588859 588859 single base substitution C T intron_variant PACA-CA 11 591461 591464 deletion of <=200bp AAGA - exon_variant PACA-CA 11 591461 591464 deletion of <=200bp AAGA - frameshift_variant LR162 PACA-CA 11 591461 591464 deletion of <=200bp AAGA - frameshift_variant LR165 PACA-CA 11 591461 591464 deletion of <=200bp AAGA - frameshift_variant LR166 PACA-CA 11 597135 597135 single base substitution G A intron_variant PACA-CA 11 597135 597135 single base substitution G A upstream_gene_variant PACA-CA 11 598385 598385 single base substitution C T exon_variant PACA-CA 11 598385 598385 single base substitution C T missense_variant R299C 895C>T PACA-CA 11 598385 598385 single base substitution C T missense_variant R302C 904C>T PACA-CA 11 598385 598385 single base substitution C T missense_variant R303C 907C>T PACA-CA 11 598385 598385 single base substitution C T upstream_gene_variant PACA-CA 11 599040 599040 single base substitution C T intron_variant PACA-CA 11 599040 599040 single base substitution C T upstream_gene_variant PACA-CA 11 600961 600961 single base substitution G A intron_variant PACA-CA 11 600961 600961 single base substitution G A upstream_gene_variant PACA-CA 11 600961 600961 single base substitution G C intron_variant PACA-CA 11 600961 600961 single base substitution G C upstream_gene_variant PACA-CA 11 600965 600965 insertion of <=200bp - A intron_variant PACA-CA 11 600965 600965 insertion of <=200bp - A upstream_gene_variant PACA-CA 11 603613 603613 single base substitution G T intron_variant PACA-CA 11 607767 607767 single base substitution G A downstream_gene_variant PACA-CA 11 607767 607767 single base substitution G A exon_variant PACA-CA 11 607767 607767 single base substitution G A missense_variant G767R 2299G>A PACA-CA 11 607767 607767 single base substitution G A missense_variant G769R 2305G>A PACA-CA 11 607767 607767 single base substitution G A missense_variant G770R 2308G>A PACA-CA 11 607767 607767 single base substitution G A missense_variant G771R 2311G>A PACA-CA 11 608890 608890 single base substitution G A downstream_gene_variant PACA-CA 11 608890 608890 single base substitution G A exon_variant PACA-CA 11 608890 608890 single base substitution G A missense_variant R1141Q 3422G>A PACA-CA 11 608890 608890 single base substitution G A missense_variant R1143Q 3428G>A PACA-CA 11 608890 608890 single base substitution G A missense_variant R1144Q 3431G>A PACA-CA 11 608890 608890 single base substitution G A missense_variant R1145Q 3434G>A PACA-CA 11 610115 610115 single base substitution C T downstream_gene_variant PACA-CA 11 610115 610115 single base substitution C T intron_variant PACA-CA 11 612372 612372 single base substitution G A downstream_gene_variant PAEN-IT 11 612184 612184 single base substitution G A 3_prime_UTR_variant PAEN-IT 11 612184 612184 single base substitution G A downstream_gene_variant PBCA-DE 11 573762 573762 single base substitution C T upstream_gene_variant PBCA-DE 11 576738 576738 single base substitution C A intron_variant PBCA-DE 11 588919 588919 insertion of <=200bp - CC intron_variant PBCA-DE 11 596765 596765 single base substitution G A intron_variant PBCA-DE 11 596765 596765 single base substitution G A upstream_gene_variant PBCA-DE 11 598487 598487 single base substitution C T exon_variant PBCA-DE 11 598487 598487 single base substitution C T missense_variant R333W 997C>T PBCA-DE 11 598487 598487 single base substitution C T missense_variant R336W 1006C>T PBCA-DE 11 598487 598487 single base substitution C T missense_variant R337W 1009C>T PBCA-DE 11 598487 598487 single base substitution C T upstream_gene_variant PBCA-DE 11 602750 602750 single base substitution G T intron_variant PBCA-DE 11 609429 609429 single base substitution T C downstream_gene_variant PBCA-DE 11 609429 609429 single base substitution T C exon_variant PBCA-DE 11 609429 609429 single base substitution T C synonymous_variant L1321L 3961T>C PBCA-DE 11 609429 609429 single base substitution T C synonymous_variant L1323L 3967T>C PBCA-DE 11 609429 609429 single base substitution T C synonymous_variant L1324L 3970T>C PBCA-DE 11 609429 609429 single base substitution T C synonymous_variant L1325L 3973T>C PBCA-DE 11 616164 616164 deletion of <=200bp A - downstream_gene_variant PRAD-CA 11 574178 574178 single base substitution A G upstream_gene_variant PRAD-CA 11 574252 574252 single base substitution G C upstream_gene_variant PRAD-CA 11 589855 589855 single base substitution C T intron_variant PRAD-CA 11 589864 589864 single base substitution C T intron_variant PRAD-CA 11 590029 590029 single base substitution T C intron_variant PRAD-CA 11 591377 591377 single base substitution C T splice_region_variant PRAD-CA 11 593268 593268 single base substitution A G intron_variant PRAD-CA 11 593860 593860 single base substitution C T intron_variant PRAD-CA 11 600512 600512 single base substitution A G intron_variant PRAD-CA 11 600512 600512 single base substitution A G upstream_gene_variant PRAD-CA 11 602750 602750 single base substitution G T intron_variant PRAD-CA 11 609808 609808 single base substitution A G downstream_gene_variant PRAD-CA 11 609808 609808 single base substitution A G intron_variant PRAD-UK 11 575800 575800 single base substitution T C upstream_gene_variant PRAD-UK 11 576916 576916 single base substitution A T intron_variant PRAD-UK 11 591482 591482 single base substitution T G intron_variant PRAD-UK 11 598649 598649 single base substitution C T intron_variant PRAD-UK 11 598649 598649 single base substitution C T upstream_gene_variant PRAD-UK 11 604485 604485 single base substitution G A intron_variant PRAD-UK 11 605696 605696 single base substitution G A exon_variant PRAD-UK 11 605696 605696 single base substitution G A missense_variant A472T 1414G>A PRAD-UK 11 605696 605696 single base substitution G A missense_variant A474T 1420G>A PRAD-UK 11 605696 605696 single base substitution G A missense_variant A475T 1423G>A PRAD-UK 11 605696 605696 single base substitution G A missense_variant A476T 1426G>A PRAD-UK 11 609162 609162 single base substitution G A downstream_gene_variant PRAD-UK 11 609162 609162 single base substitution G A exon_variant PRAD-UK 11 609162 609162 single base substitution G A missense_variant D1232N 3694G>A PRAD-UK 11 609162 609162 single base substitution G A missense_variant D1234N 3700G>A PRAD-UK 11 609162 609162 single base substitution G A missense_variant D1235N 3703G>A PRAD-UK 11 609162 609162 single base substitution G A missense_variant D1236N 3706G>A PRAD-UK 11 609578 609578 single base substitution G A downstream_gene_variant PRAD-UK 11 609578 609578 single base substitution G A exon_variant PRAD-UK 11 609578 609578 single base substitution G A synonymous_variant A1370A 4110G>A PRAD-UK 11 609578 609578 single base substitution G A synonymous_variant A1372A 4116G>A PRAD-UK 11 609578 609578 single base substitution G A synonymous_variant A1373A 4119G>A PRAD-UK 11 609578 609578 single base substitution G A synonymous_variant A1374A 4122G>A PRAD-US 11 607296 607296 single base substitution C A downstream_gene_variant PRAD-US 11 607296 607296 single base substitution C A exon_variant PRAD-US 11 607296 607296 single base substitution C A synonymous_variant R610R 1828C>A PRAD-US 11 607296 607296 single base substitution C A synonymous_variant R612R 1834C>A PRAD-US 11 607296 607296 single base substitution C A synonymous_variant R613R 1837C>A PRAD-US 11 607296 607296 single base substitution C A synonymous_variant R614R 1840C>A PRAD-US 11 608013 608013 single base substitution G A downstream_gene_variant PRAD-US 11 608013 608013 single base substitution G A exon_variant PRAD-US 11 608013 608013 single base substitution G A missense_variant G849S 2545G>A PRAD-US 11 608013 608013 single base substitution G A missense_variant G851S 2551G>A PRAD-US 11 608013 608013 single base substitution G A missense_variant G852S 2554G>A PRAD-US 11 608013 608013 single base substitution G A missense_variant G853S 2557G>A READ-US 11 607979 607979 single base substitution C T downstream_gene_variant READ-US 11 607979 607979 single base substitution C T exon_variant READ-US 11 607979 607979 single base substitution C T synonymous_variant S837S 2511C>T READ-US 11 607979 607979 single base substitution C T synonymous_variant S839S 2517C>T READ-US 11 607979 607979 single base substitution C T synonymous_variant S840S 2520C>T READ-US 11 607979 607979 single base substitution C T synonymous_variant S841S 2523C>T READ-US 11 608730 608730 single base substitution C T downstream_gene_variant READ-US 11 608730 608730 single base substitution C T exon_variant READ-US 11 608730 608730 single base substitution C T missense_variant R1088W 3262C>T READ-US 11 608730 608730 single base substitution C T missense_variant R1090W 3268C>T READ-US 11 608730 608730 single base substitution C T missense_variant R1091W 3271C>T READ-US 11 608730 608730 single base substitution C T missense_variant R1092W 3274C>T READ-US 11 609553 609553 single base substitution C T downstream_gene_variant READ-US 11 609553 609553 single base substitution C T exon_variant READ-US 11 609553 609553 single base substitution C T missense_variant A1362V 4085C>T READ-US 11 609553 609553 single base substitution C T missense_variant A1364V 4091C>T READ-US 11 609553 609553 single base substitution C T missense_variant A1365V 4094C>T READ-US 11 609553 609553 single base substitution C T missense_variant A1366V 4097C>T RECA-EU 11 577539 577539 single base substitution T G intron_variant RECA-EU 11 586070 586070 single base substitution A T intron_variant RECA-EU 11 598951 598951 single base substitution T C intron_variant RECA-EU 11 598951 598951 single base substitution T C upstream_gene_variant RECA-EU 11 599352 599352 single base substitution G A intron_variant RECA-EU 11 599352 599352 single base substitution G A upstream_gene_variant RECA-EU 11 604706 604706 single base substitution G A intron_variant RECA-EU 11 608970 608970 single base substitution G C downstream_gene_variant RECA-EU 11 608970 608970 single base substitution G C exon_variant RECA-EU 11 608970 608970 single base substitution G C missense_variant A1168P 3502G>C RECA-EU 11 608970 608970 single base substitution G C missense_variant A1170P 3508G>C RECA-EU 11 608970 608970 single base substitution G C missense_variant A1171P 3511G>C RECA-EU 11 608970 608970 single base substitution G C missense_variant A1172P 3514G>C SKCA-BR 11 574783 574783 single base substitution A C upstream_gene_variant SKCA-BR 11 574801 574801 single base substitution T C upstream_gene_variant SKCA-BR 11 574805 574805 single base substitution T C upstream_gene_variant SKCA-BR 11 579257 579257 single base substitution C T intron_variant SKCA-BR 11 579458 579458 single base substitution A T intron_variant SKCA-BR 11 581402 581402 single base substitution A G intron_variant SKCA-BR 11 583399 583399 single base substitution C T intron_variant SKCA-BR 11 583731 583735 deletion of <=200bp TCAAA - intron_variant SKCA-BR 11 584112 584112 single base substitution G A intron_variant SKCA-BR 11 585543 585543 single base substitution T A intron_variant SKCA-BR 11 585640 585640 single base substitution G A intron_variant SKCA-BR 11 586655 586655 single base substitution G A intron_variant SKCA-BR 11 587779 587779 single base substitution T G intron_variant SKCA-BR 11 589380 589380 single base substitution T G intron_variant SKCA-BR 11 589579 589579 insertion of <=200bp - GGA intron_variant SKCA-BR 11 589855 589855 single base substitution C T intron_variant SKCA-BR 11 590102 590102 single base substitution G C intron_variant SKCA-BR 11 593504 593504 single base substitution A C intron_variant SKCA-BR 11 597071 597071 single base substitution A T intron_variant SKCA-BR 11 597071 597071 single base substitution A T upstream_gene_variant SKCA-BR 11 602770 602770 insertion of <=200bp - GT intron_variant SKCA-BR 11 603728 603729 deletion of <=200bp TG - intron_variant SKCA-BR 11 603776 603776 single base substitution T C intron_variant SKCA-BR 11 604964 604964 single base substitution G A intron_variant SKCA-BR 11 606790 606790 single base substitution C T exon_variant SKCA-BR 11 606790 606790 single base substitution C T intron_variant SKCA-BR 11 606900 606900 single base substitution T G downstream_gene_variant SKCA-BR 11 606900 606900 single base substitution T G intron_variant SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - downstream_gene_variant SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - exon_variant SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - frameshift_variant RTRSG1012 SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - frameshift_variant RTRSG1014 SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - frameshift_variant RTRSG1015 SKCA-BR 11 608502 608514 deletion of <=200bp CGGACGCGCTCTG - frameshift_variant RTRSG1016 SKCA-BR 11 608921 608921 single base substitution C T downstream_gene_variant SKCA-BR 11 608921 608921 single base substitution C T exon_variant SKCA-BR 11 608921 608921 single base substitution C T synonymous_variant P1151P 3453C>T SKCA-BR 11 608921 608921 single base substitution C T synonymous_variant P1153P 3459C>T SKCA-BR 11 608921 608921 single base substitution C T synonymous_variant P1154P 3462C>T SKCA-BR 11 608921 608921 single base substitution C T synonymous_variant P1155P 3465C>T SKCA-BR 11 609760 609760 single base substitution A C downstream_gene_variant SKCA-BR 11 609760 609760 single base substitution A C intron_variant SKCA-BR 11 609774 609774 single base substitution T C downstream_gene_variant SKCA-BR 11 609774 609774 single base substitution T C intron_variant SKCA-BR 11 615669 615669 single base substitution C A downstream_gene_variant SKCA-BR 11 617126 617126 single base substitution T G downstream_gene_variant SKCM-US 11 587263 587263 single base substitution C T exon_variant SKCM-US 11 587263 587263 single base substitution C T synonymous_variant S69S 207C>T SKCM-US 11 587263 587263 single base substitution C T synonymous_variant S72S 216C>T SKCM-US 11 587263 587263 single base substitution C T synonymous_variant S73S 219C>T SKCM-US 11 587401 587401 single base substitution C A exon_variant SKCM-US 11 587401 587401 single base substitution C A synonymous_variant A115A 345C>A SKCM-US 11 587401 587401 single base substitution C A synonymous_variant A118A 354C>A SKCM-US 11 587401 587401 single base substitution C A synonymous_variant A119A 357C>A SKCM-US 11 587429 587429 single base substitution T G exon_variant SKCM-US 11 587429 587429 single base substitution T G missense_variant Y125D 373T>G SKCM-US 11 587429 587429 single base substitution T G missense_variant Y128D 382T>G SKCM-US 11 587429 587429 single base substitution T G missense_variant Y129D 385T>G SKCM-US 11 591394 591394 single base substitution C T exon_variant SKCM-US 11 591394 591394 single base substitution C T missense_variant S140F 419C>T SKCM-US 11 591394 591394 single base substitution C T missense_variant S143F 428C>T SKCM-US 11 591394 591394 single base substitution C T missense_variant S144F 431C>T SKCM-US 11 591435 591435 single base substitution C T exon_variant SKCM-US 11 591435 591435 single base substitution C T stop_gained R154* 460C>T SKCM-US 11 591435 591435 single base substitution C T stop_gained R157* 469C>T SKCM-US 11 591435 591435 single base substitution C T stop_gained R158* 472C>T SKCM-US 11 597425 597425 single base substitution C T exon_variant SKCM-US 11 597425 597425 single base substitution C T missense_variant S246F 737C>T SKCM-US 11 597425 597425 single base substitution C T missense_variant S249F 746C>T SKCM-US 11 597425 597425 single base substitution C T missense_variant S250F 749C>T SKCM-US 11 597425 597425 single base substitution C T upstream_gene_variant SKCM-US 11 598398 598398 single base substitution C T exon_variant SKCM-US 11 598398 598398 single base substitution C T missense_variant S303F 908C>T SKCM-US 11 598398 598398 single base substitution C T missense_variant S306F 917C>T SKCM-US 11 598398 598398 single base substitution C T missense_variant S307F 920C>T SKCM-US 11 598398 598398 single base substitution C T upstream_gene_variant SKCM-US 11 605145 605145 single base substitution C T exon_variant SKCM-US 11 605145 605145 single base substitution C T synonymous_variant I389I 1167C>T SKCM-US 11 605145 605145 single base substitution C T synonymous_variant I392I 1176C>T SKCM-US 11 605145 605145 single base substitution C T synonymous_variant I393I 1179C>T SKCM-US 11 605665 605665 single base substitution C T exon_variant SKCM-US 11 605665 605665 single base substitution C T synonymous_variant S461S 1383C>T SKCM-US 11 605665 605665 single base substitution C T synonymous_variant S463S 1389C>T SKCM-US 11 605665 605665 single base substitution C T synonymous_variant S464S 1392C>T SKCM-US 11 605665 605665 single base substitution C T synonymous_variant S465S 1395C>T SKCM-US 11 607121 607121 single base substitution C T downstream_gene_variant SKCM-US 11 607121 607121 single base substitution C T exon_variant SKCM-US 11 607121 607121 single base substitution C T synonymous_variant F551F 1653C>T SKCM-US 11 607121 607121 single base substitution C T synonymous_variant F553F 1659C>T SKCM-US 11 607121 607121 single base substitution C T synonymous_variant F554F 1662C>T SKCM-US 11 607121 607121 single base substitution C T synonymous_variant F555F 1665C>T SKCM-US 11 607444 607444 single base substitution C T downstream_gene_variant SKCM-US 11 607444 607444 single base substitution C T exon_variant SKCM-US 11 607444 607444 single base substitution C T missense_variant P659L 1976C>T SKCM-US 11 607444 607444 single base substitution C T missense_variant P661L 1982C>T SKCM-US 11 607444 607444 single base substitution C T missense_variant P662L 1985C>T SKCM-US 11 607444 607444 single base substitution C T missense_variant P663L 1988C>T SKCM-US 11 607720 607720 single base substitution C T downstream_gene_variant SKCM-US 11 607720 607720 single base substitution C T exon_variant SKCM-US 11 607720 607720 single base substitution C T missense_variant S751F 2252C>T SKCM-US 11 607720 607720 single base substitution C T missense_variant S753F 2258C>T SKCM-US 11 607720 607720 single base substitution C T missense_variant S754F 2261C>T SKCM-US 11 607720 607720 single base substitution C T missense_variant S755F 2264C>T SKCM-US 11 607766 607766 single base substitution C T downstream_gene_variant SKCM-US 11 607766 607766 single base substitution C T exon_variant SKCM-US 11 607766 607766 single base substitution C T synonymous_variant V766V 2298C>T SKCM-US 11 607766 607766 single base substitution C T synonymous_variant V768V 2304C>T SKCM-US 11 607766 607766 single base substitution C T synonymous_variant V769V 2307C>T SKCM-US 11 607766 607766 single base substitution C T synonymous_variant V770V 2310C>T SKCM-US 11 608545 608545 single base substitution C T downstream_gene_variant SKCM-US 11 608545 608545 single base substitution C T exon_variant SKCM-US 11 608545 608545 single base substitution C T missense_variant S1026L 3077C>T SKCM-US 11 608545 608545 single base substitution C T missense_variant S1028L 3083C>T SKCM-US 11 608545 608545 single base substitution C T missense_variant S1029L 3086C>T SKCM-US 11 608545 608545 single base substitution C T missense_variant S1030L 3089C>T SKCM-US 11 608886 608886 single base substitution G A downstream_gene_variant SKCM-US 11 608886 608886 single base substitution G A exon_variant SKCM-US 11 608886 608886 single base substitution G A missense_variant E1140K 3418G>A SKCM-US 11 608886 608886 single base substitution G A missense_variant E1142K 3424G>A SKCM-US 11 608886 608886 single base substitution G A missense_variant E1143K 3427G>A SKCM-US 11 608886 608886 single base substitution G A missense_variant E1144K 3430G>A SKCM-US 11 608893 608893 single base substitution C T downstream_gene_variant SKCM-US 11 608893 608893 single base substitution C T exon_variant SKCM-US 11 608893 608893 single base substitution C T missense_variant P1142L 3425C>T SKCM-US 11 608893 608893 single base substitution C T missense_variant P1144L 3431C>T SKCM-US 11 608893 608893 single base substitution C T missense_variant P1145L 3434C>T SKCM-US 11 608893 608893 single base substitution C T missense_variant P1146L 3437C>T SKCM-US 11 608919 608919 single base substitution C T downstream_gene_variant SKCM-US 11 608919 608919 single base substitution C T exon_variant SKCM-US 11 608919 608919 single base substitution C T missense_variant P1151S 3451C>T SKCM-US 11 608919 608919 single base substitution C T missense_variant P1153S 3457C>T SKCM-US 11 608919 608919 single base substitution C T missense_variant P1154S 3460C>T SKCM-US 11 608919 608919 single base substitution C T missense_variant P1155S 3463C>T SKCM-US 11 609122 609122 single base substitution C T downstream_gene_variant SKCM-US 11 609122 609122 single base substitution C T exon_variant SKCM-US 11 609122 609122 single base substitution C T synonymous_variant A1218A 3654C>T SKCM-US 11 609122 609122 single base substitution C T synonymous_variant A1220A 3660C>T SKCM-US 11 609122 609122 single base substitution C T synonymous_variant A1221A 3663C>T SKCM-US 11 609122 609122 single base substitution C T synonymous_variant A1222A 3666C>T SKCM-US 11 609185 609185 single base substitution C T downstream_gene_variant SKCM-US 11 609185 609185 single base substitution C T exon_variant SKCM-US 11 609185 609185 single base substitution C T synonymous_variant P1239P 3717C>T SKCM-US 11 609185 609185 single base substitution C T synonymous_variant P1241P 3723C>T SKCM-US 11 609185 609185 single base substitution C T synonymous_variant P1242P 3726C>T SKCM-US 11 609185 609185 single base substitution C T synonymous_variant P1243P 3729C>T SKCM-US 11 609451 609451 single base substitution C T downstream_gene_variant SKCM-US 11 609451 609451 single base substitution C T exon_variant SKCM-US 11 609451 609451 single base substitution C T missense_variant S1328L 3983C>T SKCM-US 11 609451 609451 single base substitution C T missense_variant S1330L 3989C>T SKCM-US 11 609451 609451 single base substitution C T missense_variant S1331L 3992C>T SKCM-US 11 609451 609451 single base substitution C T missense_variant S1332L 3995C>T SKCM-US 11 611069 611069 single base substitution A G 3_prime_UTR_variant SKCM-US 11 611069 611069 single base substitution A G downstream_gene_variant SKCM-US 11 611069 611069 single base substitution A G missense_variant K1594R 4781A>G SKCM-US 11 611069 611069 single base substitution A G missense_variant K1596R 4787A>G SKCM-US 11 611069 611069 single base substitution A G missense_variant K1597R 4790A>G SKCM-US 11 611069 611069 single base substitution A G missense_variant K1598R 4793A>G SKCM-US 11 612695 612695 single base substitution G A downstream_gene_variant SKCM-US 11 612716 612716 single base substitution A G downstream_gene_variant SKCM-US 11 613290 613290 single base substitution C T downstream_gene_variant SKCM-US 11 615007 615007 single base substitution C T downstream_gene_variant SKCM-US 11 615225 615225 single base substitution G A downstream_gene_variant STAD-US 11 582040 582040 single base substitution A G exon_variant STAD-US 11 582040 582040 single base substitution A G missense_variant D54G 161A>G STAD-US 11 582040 582040 single base substitution A G missense_variant D57G 170A>G STAD-US 11 582040 582040 single base substitution A G missense_variant D58G 173A>G STAD-US 11 592628 592628 single base substitution A G exon_variant STAD-US 11 592628 592628 single base substitution A G missense_variant S188G 562A>G STAD-US 11 592628 592628 single base substitution A G missense_variant S191G 571A>G STAD-US 11 592628 592628 single base substitution A G missense_variant S192G 574A>G STAD-US 11 596998 596998 single base substitution G A exon_variant STAD-US 11 596998 596998 single base substitution G A synonymous_variant A228A 684G>A STAD-US 11 596998 596998 single base substitution G A synonymous_variant A231A 693G>A STAD-US 11 596998 596998 single base substitution G A synonymous_variant A232A 696G>A STAD-US 11 596998 596998 single base substitution G A upstream_gene_variant STAD-US 11 598394 598394 single base substitution T A exon_variant STAD-US 11 598394 598394 single base substitution T A missense_variant S302T 904T>A STAD-US 11 598394 598394 single base substitution T A missense_variant S305T 913T>A STAD-US 11 598394 598394 single base substitution T A missense_variant S306T 916T>A STAD-US 11 598394 598394 single base substitution T A upstream_gene_variant STAD-US 11 598413 598413 single base substitution C T exon_variant STAD-US 11 598413 598413 single base substitution C T missense_variant A308V 923C>T STAD-US 11 598413 598413 single base substitution C T missense_variant A311V 932C>T STAD-US 11 598413 598413 single base substitution C T missense_variant A312V 935C>T STAD-US 11 598413 598413 single base substitution C T upstream_gene_variant STAD-US 11 598418 598418 single base substitution G A exon_variant STAD-US 11 598418 598418 single base substitution G A missense_variant E310K 928G>A STAD-US 11 598418 598418 single base substitution G A missense_variant E313K 937G>A STAD-US 11 598418 598418 single base substitution G A missense_variant E314K 940G>A STAD-US 11 598418 598418 single base substitution G A upstream_gene_variant STAD-US 11 598487 598487 single base substitution C T exon_variant STAD-US 11 598487 598487 single base substitution C T missense_variant R333W 997C>T STAD-US 11 598487 598487 single base substitution C T missense_variant R336W 1006C>T STAD-US 11 598487 598487 single base substitution C T missense_variant R337W 1009C>T STAD-US 11 598487 598487 single base substitution C T upstream_gene_variant STAD-US 11 601629 601629 single base substitution A T exon_variant STAD-US 11 601629 601629 single base substitution A T missense_variant K356N 1068A>T STAD-US 11 601629 601629 single base substitution A T missense_variant K359N 1077A>T STAD-US 11 601629 601629 single base substitution A T missense_variant K360N 1080A>T STAD-US 11 601629 601629 single base substitution A T upstream_gene_variant STAD-US 11 605153 605153 single base substitution C T exon_variant STAD-US 11 605153 605153 single base substitution C T missense_variant T392M 1175C>T STAD-US 11 605153 605153 single base substitution C T missense_variant T395M 1184C>T STAD-US 11 605153 605153 single base substitution C T missense_variant T396M 1187C>T STAD-US 11 605238 605238 single base substitution G A exon_variant STAD-US 11 605238 605238 single base substitution G A synonymous_variant A420A 1260G>A STAD-US 11 605238 605238 single base substitution G A synonymous_variant A423A 1269G>A STAD-US 11 605238 605238 single base substitution G A synonymous_variant A424A 1272G>A STAD-US 11 607110 607112 deletion of <=200bp GAA - downstream_gene_variant STAD-US 11 607110 607112 deletion of <=200bp GAA - exon_variant STAD-US 11 607110 607112 deletion of <=200bp GAA - inframe_deletion E548 STAD-US 11 607110 607112 deletion of <=200bp GAA - inframe_deletion E550 STAD-US 11 607110 607112 deletion of <=200bp GAA - inframe_deletion E551 STAD-US 11 607110 607112 deletion of <=200bp GAA - inframe_deletion E552 STAD-US 11 607264 607264 single base substitution A G downstream_gene_variant STAD-US 11 607264 607264 single base substitution A G exon_variant STAD-US 11 607264 607264 single base substitution A G missense_variant D599G 1796A>G STAD-US 11 607264 607264 single base substitution A G missense_variant D601G 1802A>G STAD-US 11 607264 607264 single base substitution A G missense_variant D602G 1805A>G STAD-US 11 607264 607264 single base substitution A G missense_variant D603G 1808A>G STAD-US 11 607394 607394 single base substitution G A downstream_gene_variant STAD-US 11 607394 607394 single base substitution G A exon_variant STAD-US 11 607394 607394 single base substitution G A synonymous_variant A642A 1926G>A STAD-US 11 607394 607394 single base substitution G A synonymous_variant A644A 1932G>A STAD-US 11 607394 607394 single base substitution G A synonymous_variant A645A 1935G>A STAD-US 11 607394 607394 single base substitution G A synonymous_variant A646A 1938G>A STAD-US 11 607923 607923 single base substitution A G downstream_gene_variant STAD-US 11 607923 607923 single base substitution A G exon_variant STAD-US 11 607923 607923 single base substitution A G missense_variant K819E 2455A>G STAD-US 11 607923 607923 single base substitution A G missense_variant K821E 2461A>G STAD-US 11 607923 607923 single base substitution A G missense_variant K822E 2464A>G STAD-US 11 607923 607923 single base substitution A G missense_variant K823E 2467A>G STAD-US 11 608145 608145 single base substitution G A downstream_gene_variant STAD-US 11 608145 608145 single base substitution G A exon_variant STAD-US 11 608145 608145 single base substitution G A missense_variant G893R 2677G>A STAD-US 11 608145 608145 single base substitution G A missense_variant G895R 2683G>A STAD-US 11 608145 608145 single base substitution G A missense_variant G896R 2686G>A STAD-US 11 608145 608145 single base substitution G A missense_variant G897R 2689G>A STAD-US 11 608437 608437 single base substitution G A downstream_gene_variant STAD-US 11 608437 608437 single base substitution G A exon_variant STAD-US 11 608437 608437 single base substitution G A missense_variant R990H 2969G>A STAD-US 11 608437 608437 single base substitution G A missense_variant R992H 2975G>A STAD-US 11 608437 608437 single base substitution G A missense_variant R993H 2978G>A STAD-US 11 608437 608437 single base substitution G A missense_variant R994H 2981G>A STAD-US 11 608501 608501 single base substitution A G downstream_gene_variant STAD-US 11 608501 608501 single base substitution A G exon_variant STAD-US 11 608501 608501 single base substitution A G synonymous_variant G1011G 3033A>G STAD-US 11 608501 608501 single base substitution A G synonymous_variant G1013G 3039A>G STAD-US 11 608501 608501 single base substitution A G synonymous_variant G1014G 3042A>G STAD-US 11 608501 608501 single base substitution A G synonymous_variant G1015G 3045A>G STAD-US 11 608885 608885 single base substitution C T downstream_gene_variant STAD-US 11 608885 608885 single base substitution C T exon_variant STAD-US 11 608885 608885 single base substitution C T synonymous_variant H1139H 3417C>T STAD-US 11 608885 608885 single base substitution C T synonymous_variant H1141H 3423C>T STAD-US 11 608885 608885 single base substitution C T synonymous_variant H1142H 3426C>T STAD-US 11 608885 608885 single base substitution C T synonymous_variant H1143H 3429C>T STAD-US 11 609019 609019 single base substitution G A downstream_gene_variant STAD-US 11 609019 609019 single base substitution G A exon_variant STAD-US 11 609019 609019 single base substitution G A missense_variant R1184Q 3551G>A STAD-US 11 609019 609019 single base substitution G A missense_variant R1186Q 3557G>A STAD-US 11 609019 609019 single base substitution G A missense_variant R1187Q 3560G>A STAD-US 11 609019 609019 single base substitution G A missense_variant R1188Q 3563G>A STAD-US 11 609248 609248 single base substitution C T downstream_gene_variant STAD-US 11 609248 609248 single base substitution C T exon_variant STAD-US 11 609248 609248 single base substitution C T synonymous_variant S1260S 3780C>T STAD-US 11 609248 609248 single base substitution C T synonymous_variant S1262S 3786C>T STAD-US 11 609248 609248 single base substitution C T synonymous_variant S1263S 3789C>T STAD-US 11 609248 609248 single base substitution C T synonymous_variant S1264S 3792C>T STAD-US 11 609301 609301 single base substitution A T downstream_gene_variant STAD-US 11 609301 609301 single base substitution A T exon_variant STAD-US 11 609301 609301 single base substitution A T missense_variant Q1278L 3833A>T STAD-US 11 609301 609301 single base substitution A T missense_variant Q1280L 3839A>T STAD-US 11 609301 609301 single base substitution A T missense_variant Q1281L 3842A>T STAD-US 11 609301 609301 single base substitution A T missense_variant Q1282L 3845A>T STAD-US 11 610707 610709 deletion of <=200bp GGA - downstream_gene_variant STAD-US 11 610707 610709 deletion of <=200bp GGA - exon_variant STAD-US 11 610707 610709 deletion of <=200bp GGA - inframe_deletion SE1537S STAD-US 11 610707 610709 deletion of <=200bp GGA - inframe_deletion SE1539S STAD-US 11 610707 610709 deletion of <=200bp GGA - inframe_deletion SE1540S STAD-US 11 610707 610709 deletion of <=200bp GGA - inframe_deletion SE1541S STAD-US 11 613969 613969 single base substitution G C downstream_gene_variant THCA-SA 11 608866 608866 single base substitution A G downstream_gene_variant THCA-SA 11 608866 608866 single base substitution A G exon_variant THCA-SA 11 608866 608866 single base substitution A G missense_variant H1133R 3398A>G THCA-SA 11 608866 608866 single base substitution A G missense_variant H1135R 3404A>G THCA-SA 11 608866 608866 single base substitution A G missense_variant H1136R 3407A>G THCA-SA 11 608866 608866 single base substitution A G missense_variant H1137R 3410A>G THCA-SA 11 609572 609572 single base substitution C G downstream_gene_variant THCA-SA 11 609572 609572 single base substitution C G exon_variant THCA-SA 11 609572 609572 single base substitution C G synonymous_variant P1368P 4104C>G THCA-SA 11 609572 609572 single base substitution C G synonymous_variant P1370P 4110C>G THCA-SA 11 609572 609572 single base substitution C G synonymous_variant P1371P 4113C>G THCA-SA 11 609572 609572 single base substitution C G synonymous_variant P1372P 4116C>G THCA-US 11 608072 608072 single base substitution G A downstream_gene_variant THCA-US 11 608072 608072 single base substitution G A exon_variant THCA-US 11 608072 608072 single base substitution G A synonymous_variant T868T 2604G>A THCA-US 11 608072 608072 single base substitution G A synonymous_variant T870T 2610G>A THCA-US 11 608072 608072 single base substitution G A synonymous_variant T871T 2613G>A THCA-US 11 608072 608072 single base substitution G A synonymous_variant T872T 2616G>A UCEC-US 11 582050 582050 single base substitution G A exon_variant UCEC-US 11 582050 582050 single base substitution G A synonymous_variant A57A 171G>A UCEC-US 11 582050 582050 single base substitution G A synonymous_variant A60A 180G>A UCEC-US 11 582050 582050 single base substitution G A synonymous_variant A61A 183G>A UCEC-US 11 587453 587453 single base substitution G A exon_variant UCEC-US 11 587453 587453 single base substitution G A missense_variant E133K 397G>A UCEC-US 11 587453 587453 single base substitution G A missense_variant E136K 406G>A UCEC-US 11 587453 587453 single base substitution G A missense_variant E137K 409G>A UCEC-US 11 591409 591409 single base substitution G A exon_variant UCEC-US 11 591409 591409 single base substitution G A missense_variant R145Q 434G>A UCEC-US 11 591409 591409 single base substitution G A missense_variant R148Q 443G>A UCEC-US 11 591409 591409 single base substitution G A missense_variant R149Q 446G>A UCEC-US 11 601669 601669 single base substitution C T exon_variant UCEC-US 11 601669 601669 single base substitution C T stop_gained R370* 1108C>T UCEC-US 11 601669 601669 single base substitution C T stop_gained R373* 1117C>T UCEC-US 11 601669 601669 single base substitution C T stop_gained R374* 1120C>T UCEC-US 11 606568 606568 single base substitution C T exon_variant UCEC-US 11 606568 606568 single base substitution C T synonymous_variant R523R 1569C>T UCEC-US 11 606568 606568 single base substitution C T synonymous_variant R525R 1575C>T UCEC-US 11 606568 606568 single base substitution C T synonymous_variant R526R 1578C>T UCEC-US 11 606568 606568 single base substitution C T synonymous_variant R527R 1581C>T UCEC-US 11 607431 607431 single base substitution C T downstream_gene_variant UCEC-US 11 607431 607431 single base substitution C T exon_variant UCEC-US 11 607431 607431 single base substitution C T missense_variant R655C 1963C>T UCEC-US 11 607431 607431 single base substitution C T missense_variant R657C 1969C>T UCEC-US 11 607431 607431 single base substitution C T missense_variant R658C 1972C>T UCEC-US 11 607431 607431 single base substitution C T missense_variant R659C 1975C>T UCEC-US 11 607474 607474 single base substitution G T downstream_gene_variant UCEC-US 11 607474 607474 single base substitution G T exon_variant UCEC-US 11 607474 607474 single base substitution G T missense_variant R669I 2006G>T UCEC-US 11 607474 607474 single base substitution G T missense_variant R671I 2012G>T UCEC-US 11 607474 607474 single base substitution G T missense_variant R672I 2015G>T UCEC-US 11 607474 607474 single base substitution G T missense_variant R673I 2018G>T UCEC-US 11 607498 607498 single base substitution G T downstream_gene_variant UCEC-US 11 607498 607498 single base substitution G T exon_variant UCEC-US 11 607498 607498 single base substitution G T missense_variant R677M 2030G>T UCEC-US 11 607498 607498 single base substitution G T missense_variant R679M 2036G>T UCEC-US 11 607498 607498 single base substitution G T missense_variant R680M 2039G>T UCEC-US 11 607498 607498 single base substitution G T missense_variant R681M 2042G>T UCEC-US 11 607787 607787 single base substitution C T downstream_gene_variant UCEC-US 11 607787 607787 single base substitution C T exon_variant UCEC-US 11 607787 607787 single base substitution C T synonymous_variant F773F 2319C>T UCEC-US 11 607787 607787 single base substitution C T synonymous_variant F775F 2325C>T UCEC-US 11 607787 607787 single base substitution C T synonymous_variant F776F 2328C>T UCEC-US 11 607787 607787 single base substitution C T synonymous_variant F777F 2331C>T UCEC-US 11 608064 608064 insertion of <=200bp - T downstream_gene_variant UCEC-US 11 608064 608064 insertion of <=200bp - T exon_variant UCEC-US 11 608064 608064 insertion of <=200bp - T frameshift_variant A866C? UCEC-US 11 608064 608064 insertion of <=200bp - T frameshift_variant A868C? UCEC-US 11 608064 608064 insertion of <=200bp - T frameshift_variant A869C? UCEC-US 11 608064 608064 insertion of <=200bp - T frameshift_variant A870C? UCEC-US 11 608470 608470 single base substitution C T downstream_gene_variant UCEC-US 11 608470 608470 single base substitution C T exon_variant UCEC-US 11 608470 608470 single base substitution C T missense_variant A1001V 3002C>T UCEC-US 11 608470 608470 single base substitution C T missense_variant A1003V 3008C>T UCEC-US 11 608470 608470 single base substitution C T missense_variant A1004V 3011C>T UCEC-US 11 608470 608470 single base substitution C T missense_variant A1005V 3014C>T UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - downstream_gene_variant UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - exon_variant UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1012R UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1014R UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1015R UCEC-US 11 608503 608514 deletion of <=200bp GGACGCGCTCTG - inframe_deletion RTRSG1016R UCEC-US 11 608849 608849 single base substitution G A downstream_gene_variant UCEC-US 11 608849 608849 single base substitution G A exon_variant UCEC-US 11 608849 608849 single base substitution G A synonymous_variant R1127R 3381G>A UCEC-US 11 608849 608849 single base substitution G A synonymous_variant R1129R 3387G>A UCEC-US 11 608849 608849 single base substitution G A synonymous_variant R1130R 3390G>A UCEC-US 11 608849 608849 single base substitution G A synonymous_variant R1131R 3393G>A UCEC-US 11 609173 609173 single base substitution C T downstream_gene_variant UCEC-US 11 609173 609173 single base substitution C T exon_variant UCEC-US 11 609173 609173 single base substitution C T synonymous_variant P1235P 3705C>T UCEC-US 11 609173 609173 single base substitution C T synonymous_variant P1237P 3711C>T UCEC-US 11 609173 609173 single base substitution C T synonymous_variant P1238P 3714C>T UCEC-US 11 609173 609173 single base substitution C T synonymous_variant P1239P 3717C>T UCEC-US 11 609285 609285 single base substitution G A downstream_gene_variant UCEC-US 11 609285 609285 single base substitution G A exon_variant UCEC-US 11 609285 609285 single base substitution G A missense_variant D1273N 3817G>A UCEC-US 11 609285 609285 single base substitution G A missense_variant D1275N 3823G>A UCEC-US 11 609285 609285 single base substitution G A missense_variant D1276N 3826G>A UCEC-US 11 609285 609285 single base substitution G A missense_variant D1277N 3829G>A UCEC-US 11 609696 609696 single base substitution G A downstream_gene_variant UCEC-US 11 609696 609696 single base substitution G A exon_variant UCEC-US 11 609696 609696 single base substitution G A missense_variant A1410T 4228G>A UCEC-US 11 609696 609696 single base substitution G A missense_variant A1412T 4234G>A UCEC-US 11 609696 609696 single base substitution G A missense_variant A1413T 4237G>A UCEC-US 11 609696 609696 single base substitution G A missense_variant A1414T 4240G>A UCEC-US 11 610285 610285 single base substitution G A downstream_gene_variant UCEC-US 11 610285 610285 single base substitution G A exon_variant UCEC-US 11 610285 610285 single base substitution G A missense_variant E1448K 4342G>A UCEC-US 11 610285 610285 single base substitution G A missense_variant E1450K 4348G>A UCEC-US 11 610285 610285 single base substitution G A missense_variant E1451K 4351G>A UCEC-US 11 610285 610285 single base substitution G A missense_variant E1452K 4354G>A UCEC-US 11 610557 610557 single base substitution C T downstream_gene_variant UCEC-US 11 610557 610557 single base substitution C T intron_variant UCEC-US 11 610557 610557 single base substitution C T synonymous_variant C1487C 4461C>T UCEC-US 11 610557 610557 single base substitution C T synonymous_variant C1489C 4467C>T UCEC-US 11 610557 610557 single base substitution C T synonymous_variant C1490C 4470C>T UCEC-US 11 610557 610557 single base substitution C T synonymous_variant C1491C 4473C>T UCEC-US 11 610651 610651 single base substitution G A downstream_gene_variant UCEC-US 11 610651 610651 single base substitution G A intron_variant UCEC-US 11 610651 610651 single base substitution G A missense_variant A1519T 4555G>A UCEC-US 11 610651 610651 single base substitution G A missense_variant A1521T 4561G>A UCEC-US 11 610651 610651 single base substitution G A missense_variant A1522T 4564G>A UCEC-US 11 610651 610651 single base substitution G A missense_variant A1523T 4567G>A UCEC-US 11 611774 611774 single base substitution C A 3_prime_UTR_variant UCEC-US 11 611774 611774 single base substitution C A downstream_gene_variant UCEC-US 11 611774 611774 single base substitution C A synonymous_variant G1645G 4935C>A UCEC-US 11 611774 611774 single base substitution C A synonymous_variant G1647G 4941C>A UCEC-US 11 611774 611774 single base substitution C A synonymous_variant G1648G 4944C>A UCEC-US 11 611774 611774 single base substitution C A synonymous_variant G1649G 4947C>A UCEC-US 11 612681 612681 single base substitution G A downstream_gene_variant UCEC-US 11 612704 612704 single base substitution C T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-S01413 COSM346990 c.3272G>T p.R1091L Substitution - Missense 11:608731-608731 + TCGA-D9-A6EC-06 COSM4402337 c.2307C>T p.V769V Substitution - coding silent 11:607766-607766 + TCGA-A2-A0T5-01 COSM3809731 c.4018A>C p.T1340P Substitution - Missense 11:609477-609477 + CHEWS026 COSM4574549 c.3008A>C p.K1003T Substitution - Missense 11:608467-608467 + YUNIBO COSM5372985 c.3030C>T p.S1010S Substitution - coding silent 11:608489-608489 + PT32 COSM5907581 c.1616C>T p.S539F Substitution - Missense 11:607075-607075 + AOCS-139-19-0 COSM3980474 c.1913C>A p.T638N Substitution - Missense 11:607372-607372 + Pat_01_B COSM5838945 c.1973G>C p.R658P Substitution - Missense 11:607432-607432 + 10-P1058 COSM4574545 c.2301A>G p.K767K Substitution - coding silent 11:607760-607760 + 587256 COSM1220481 c.4943G>A p.G1648D Substitution - Missense 11:611773-611773 + 12-P616 COSM4574530 c.1169G>A p.R390H Substitution - Missense 11:605135-605135 + TCGA-B5-A0JY-01 COSM929353 c.2328C>T p.F776F Substitution - coding silent 11:607787-607787 + LUAD-NYU160 COSM370389 c.2553C>T p.P851P Substitution - coding silent 11:608012-608012 + TCGA-AN-A046-01 COSM929213 c.1120C>T p.R374* Substitution - Nonsense 11:601669-601669 + BD124T COSM5492720 c.2375G>A p.S792N Substitution - Missense 11:607834-607834 + T2959 COSM4714181 c.3526C>T p.R1176W Substitution - Missense 11:608985-608985 + TCGA-AN-A0FX-01 COSM3809726 c.2666C>T p.T889I Substitution - Missense 11:608125-608125 + TCGA-D1-A103-01 COSM929456 c.4944C>A p.G1648G Substitution - coding silent 11:611774-611774 + 2521262 COSM5892145 c.1207G>T p.V403F Substitution - Missense 11:605173-605173 + HT115 COSM929014 c.446G>A p.R149Q Substitution - Missense 11:591409-591409 + CSCC-31-T COSM4470171 c.1644C>T p.S548S Substitution - coding silent 11:607103-607103 + RK092_C01 COSM1628114 c.1657G>T p.G553* Substitution - Nonsense 11:607116-607116 + HCT15 COSM4622205 c.4442C>A p.P1481Q Substitution - Missense 11:610529-610529 + HCC167 COSM3666463 c.4358C>T p.P1453L Substitution - Missense 11:610292-610292 + TCGA-D3-A3MR-06 COSM3450530 c.1392C>T p.S464S Substitution - coding silent 11:605665-605665 + DLD1 COSM4622200 c.2154C>A p.G718G Substitution - coding silent 11:607613-607613 + PD6733b COSM5785594 c.3378C>A p.S1126R Substitution - Missense 11:608837-608837 + CSCC-49-T COSM4559244 c.797G>T p.R266L Substitution - Missense 11:597473-597473 + ESCC_144 COSM5644523 c.1A>G p.M1V Substitution - Missense 11:581513-581513 + CSCC-58-T COSM4485493 c.293C>T p.S98F Substitution - Missense 11:587337-587337 + Pat_59_A COSM5838911 c.878C>T p.T293M Substitution - Missense 11:597554-597554 + TCGA-D1-A0ZO-01 COSM929372 c.2730C>T p.A910A Substitution - coding silent 11:608189-608189 + SNUH_G26_S1 COSM3998492 c.381C>A p.A127A Substitution - coding silent 11:587425-587425 + ESO-859 COSM1239826 c.2078G>A p.R693Q Substitution - Missense 11:607537-607537 + 075T COSM1730617 c.2429A>G p.E810G Substitution - Missense 11:607888-607888 + T207 COSM2036974 c.2713C>T p.R905W Substitution - Missense 11:608172-608172 + TCGA-EE-A3AD-06 COSM3450226 c.472C>T p.R158* Substitution - Nonsense 11:591435-591435 + PAPNNX COSM5005067 c.856G>A p.V286M Substitution - Missense 11:597532-597532 + ESCC_68 COSM5633801 c.516G>C p.E172D Substitution - Missense 11:592570-592570 + Pat_06_B COSM4714169 c.532_534delGAG p.E181delE Deletion - In frame 11:592586-592588 + TCGA-FS-A1Z3-06 COSM3450659 c.3726C>T p.P1242P Substitution - coding silent 11:609185-609185 + TCGA-BR-8683-01 COSM4034549 c.3042A>G p.G1014G Substitution - coding silent 11:608501-608501 + 587350 COSM1220477 c.3862C>G p.P1288A Substitution - Missense 11:609321-609321 + ESCC_BICR_051T COSM5443946 c.756C>A p.L252L Substitution - coding silent 11:597432-597432 + TCGA-MI-A75C-01 COSM4923121 c.3539G>T p.R1180L Substitution - Missense 11:608998-608998 + T3174 COSM4714165 c.35G>A p.R12Q Substitution - Missense 11:581547-581547 + ESCC_134 COSM5642671 c.2123C>G p.A708G Substitution - Missense 11:607582-607582 + CHC1756T COSM4804512 c.1605G>T p.A535A Substitution - coding silent 11:606595-606595 + TCGA-29-1703-01 COSM1322349 c.556T>A p.C186S Substitution - Missense 11:592610-592610 + TCGA-BR-4292-01 COSM2036994 c.2978G>A p.R993H Substitution - Missense 11:608437-608437 + I2L-P10-Tumor-Organoid COSM5360480 c.2098G>A p.G700R Substitution - Missense 11:607557-607557 + Pat_37_B COSM3450372 c.920C>T p.S307F Substitution - Missense 11:598398-598398 + AD8 COSM5966171 c.3454G>T p.A1152S Substitution - Missense 11:608913-608913 + HCC122T COSM5808660 c.3511G>T p.A1171S Substitution - Missense 11:608970-608970 + 80 COSM5014970 c.1346C>A p.S449Y Substitution - Missense 11:605619-605619 + TCGA-C4-A0F7-01 COSM415514 c.1838G>A p.R613Q Substitution - Missense 11:607297-607297 + PTC-7C COSM4145963 c.4343T>C p.V1448A Substitution - Missense 11:610277-610277 + SC_9103 COSM5565615 c.994C>T p.R332C Substitution - Missense 11:598472-598472 + TARGET-20-PASPKE-09A-03D COSM2036159 c.1075G>A p.A359T Substitution - Missense 11:601624-601624 + NCI-H716 COSM4646970 c.3538C>T p.R1180C Substitution - Missense 11:608997-608997 + TCGA-AP-A0LM-01 COSM929417 c.4470C>T p.C1490C Substitution - coding silent 11:610557-610557 + T3262 COSM4714173 c.1681C>T p.R561* Substitution - Nonsense 11:607140-607140 + Pat_06_A COSM4714169 c.532_534delGAG p.E181delE Deletion - In frame 11:592586-592588 + 2277217 COSM4422907 c.3059_3060delCG p.R1021fs*2 Deletion - Frameshift 11:608518-608519 + HCC159T COSM3666444 c.703G>T p.V235F Substitution - Missense 11:597005-597005 + B9-Tumor COSM3931365 c.4750A>G p.R1584G Substitution - Missense 11:611029-611029 + TCGA-EE-A29D-06 COSM3450650 c.3434C>T p.P1145L Substitution - Missense 11:608893-608893 + 44 COSM5734160 c.2794C>T p.R932W Substitution - Missense 11:608253-608253 + 07-P8041 COSM4574543 c.1791G>A p.A597A Substitution - coding silent 11:607250-607250 + 08-P8005 COSM4034561 c.3789C>T p.S1263S Substitution - coding silent 11:609248-609248 + PTC_245 COSM5958571 c.3407A>G p.H1136R Substitution - Missense 11:608866-608866 + TCGA-BH-A0B6-01 COSM3809664 c.442G>A p.D148N Substitution - Missense 11:591405-591405 + TCGA-D1-A103-01 COSM929374 c.3011C>T p.A1004V Substitution - Missense 11:608470-608470 + TCGA-AP-A0LM-01 COSM929419 c.4564G>A p.A1522T Substitution - Missense 11:610651-610651 + CCC1 COSM3666442 c.662C>T p.P221L Substitution - Missense 11:596964-596964 + 35M COSM3450159 c.219C>T p.S73S Substitution - coding silent 11:587263-587263 + TCGA-G3-A5SJ-01 COSM4914830 c.336C>A p.L112L Substitution - coding silent 11:587380-587380 + 91890 COSM329527 c.3086C>T p.S1029L Substitution - Missense 11:608545-608545 + AOCS-139-12-5 COSM3980474 c.1913C>A p.T638N Substitution - Missense 11:607372-607372 + TCGA-C8-A12O-01 COSM429397 c.4710_4712delGGA p.E1572delE Deletion - In frame 11:610989-610991 + 1169-01-01TD COSM5417825 c.4555C>T p.P1519S Substitution - Missense 11:610642-610642 + BRC35 COSM5027333 c.2729C>A p.A910D Substitution - Missense 11:608188-608188 + TCGA-CG-5721-01 COSM2036428 c.1187C>T p.T396M Substitution - Missense 11:605153-605153 + pfg181T COSM4765004 c.2804_2805insC p.E938fs*5 Insertion - Frameshift 11:608263-608264 + CHC059T COSM4803088 c.3650C>G p.T1217S Substitution - Missense 11:609109-609109 + T2940 COSM4714177 c.2804delC p.P937fs*23 Deletion - Frameshift 11:608263-608263 + SNUH_G26_S1 COSM3998512 c.3894G>A p.P1298P Substitution - coding silent 11:609353-609353 + ICGC_MB79 COSM3764326 c.3970T>C p.L1324L Substitution - coding silent 11:609429-609429 + 0008_CRUK_PC_0008_T2_DNA COSM3849506 c.1423G>A p.A475T Substitution - Missense 11:605696-605696 + TCGA-EB-A431-01 COSM329527 c.3086C>T p.S1029L Substitution - Missense 11:608545-608545 + CSCC-19-T COSM929392 c.3714C>T p.P1238P Substitution - coding silent 11:609173-609173 + LC_S15 COSM1188110 c.3524G>A p.R1175K Substitution - Missense 11:608983-608983 + CRC-19T COSM5480901 c.3478C>T p.R1160W Substitution - Missense 11:608937-608937 + TCGA-EB-A431-01 COSM3450372 c.920C>T p.S307F Substitution - Missense 11:598398-598398 + PTC-28C COSM4145934 c.1003G>T p.A335S Substitution - Missense 11:598481-598481 + 6 COSM4657549 c.2696C>T p.S899F Substitution - Missense 11:608155-608155 + T2932 COSM4714171 c.647_648insA p.L217fs*24 Insertion - Frameshift 11:596949-596950 + TCGA-B5-A11E-01 COSM929392 c.3714C>T p.P1238P Substitution - coding silent 11:609173-609173 + TCGA-B5-A0K9-01 COSM929376 c.3390G>A p.R1130R Substitution - coding silent 11:608849-608849 + TCGA-BS-A0UF-01 COSM929343 c.2015G>T p.R672I Substitution - Missense 11:607474-607474 + HCC159T COSM3666446 c.706G>T p.V236F Substitution - Missense 11:597008-597008 + TCGA-DR-A0ZM-01 COSM458498 c.2749G>C p.E917Q Substitution - Missense 11:608208-608208 + TCGA-EE-A2GC-06 COSM3450620 c.2261C>T p.S754F Substitution - Missense 11:607720-607720 + TCGA-39-5022-01 COSM689356 c.2539G>A p.E847K Substitution - Missense 11:607998-607998 + 2492720 COSM5721616 c.2982C>T p.S994S Substitution - coding silent 11:608441-608441 + SNU-175 COSM2035866 c.830G>A p.R277Q Substitution - Missense 11:597506-597506 + CSCC-19-T COSM4478496 c.2242C>T p.R748W Substitution - Missense 11:607701-607701 + PDA_025 COSM4999276 c.3445G>T p.E1149* Substitution - Nonsense 11:608904-608904 + MO_1094 COSM5556004 c.2285G>C p.G762A Substitution - Missense 11:607744-607744 + TCGA-A2-A0SX-01 COSM429386 c.3044_3055del12 p.G1019_S1022delGTRS Deletion - In frame 11:608503-608514 + CSCC-10-T COSM4479943 c.2373C>A p.S791S Substitution - coding silent 11:607832-607832 + TCGA-DJ-A3UX-01 COSM3368460 c.2613G>A p.T871T Substitution - coding silent 11:608072-608072 + 443 COSM4434731 c.3008A>G p.K1003R Substitution - Missense 11:608467-608467 + TCGA-AP-A1DQ-01 COSM429386 c.3044_3055del12 p.G1019_S1022delGTRS Deletion - In frame 11:608503-608514 + Pat_41_B COSM5838947 c.2246C>T p.P749L Substitution - Missense 11:607705-607705 + TCGA-28-2499-01 COSM543942 c.1934C>T p.A645V Substitution - Missense 11:607393-607393 + PTC-54C COSM429390 c.3609G>A p.A1203A Substitution - coding silent 11:609068-609068 + CSCC-31-T COSM4517198 c.2964_2965CC>TT p.P989S Substitution - Missense 11:608423-608424 + BL42 COSM3728230 c.4817A>G p.K1606R Substitution - Missense 11:611647-611647 + LOVO COSM2035018 c.323G>A p.C108Y Substitution - Missense 11:587367-587367 + Au3 COSM5602077 c.4640C>T p.P1547L Substitution - Missense 11:610727-610727 + TCGA-EE-A181-06 COSM3450614 c.1662C>T p.F554F Substitution - coding silent 11:607121-607121 + CCK81 COSM2036897 c.2351T>C p.M784T Substitution - Missense 11:607810-607810 + KM12 COSM2037148 c.4125G>A p.G1375G Substitution - coding silent 11:609584-609584 + JEKO-1 COSM1239826 c.2078G>A p.R693Q Substitution - Missense 11:607537-607537 + WSU-HN8 COSM2037106 c.3634C>T p.R1212W Substitution - Missense 11:609093-609093 + TCGA-AZ-6598-01 COSM1355079 c.3013A>C p.K1005Q Substitution - Missense 11:608472-608472 + TCGA-CD-A487-01 COSM4034547 c.2686G>A p.G896R Substitution - Missense 11:608145-608145 + PT08_2 COSM5893601 c.621-7C>T p.? Unknown 11:596916-596916 + ESCC_BICR_060T COSM5434811 c.3832G>A p.V1278I Substitution - Missense 11:609291-609291 + PD9605a COSM5772548 c.1381C>T p.R461W Substitution - Missense 11:605654-605654 + TCGA-A6-6653-01 COSM1355054 c.1438G>A p.V480M Substitution - Missense 11:605711-605711 + HCC57 COSM1604859 c.4414-8C>T p.? Unknown 11:610493-610493 + C008 COSM5523460 c.2254C>T p.P752S Substitution - Missense 11:607713-607713 + 386 COSM4427079 c.1469C>T p.A490V Substitution - Missense 11:606459-606459 + TCGA-D1-A16J-01 COSM929394 c.3826G>A p.D1276N Substitution - Missense 11:609285-609285 + 0052_CRUK_PC_0052_T1_DNA COSM5421846 c.3703G>A p.D1235N Substitution - Missense 11:609162-609162 + T1154 COSM4714175 c.2028T>C p.S676S Substitution - coding silent 11:607487-607487 + T3182 COSM4714183 c.3978C>T p.H1326H Substitution - coding silent 11:609437-609437 + HCC159 COSM3666446 c.706G>T p.V236F Substitution - Missense 11:597008-597008 + TCGA-F4-6856-01 COSM1354804 c.158G>T p.G53V Substitution - Missense 11:582025-582025 + J90_T COSM3953542 c.4105G>A p.D1369N Substitution - Missense 11:609564-609564 + SC_9047 COSM5572375 c.4772A>G p.Y1591C Substitution - Missense 11:611051-611051 + TCGA-D1-A15X-01 COSM929409 c.4351G>A p.E1451K Substitution - Missense 11:610285-610285 + TCGA-BQ-5885-01 COSM3986277 c.1090T>C p.S364P Substitution - Missense 11:601639-601639 + BCM683T COSM4799332 c.2229C>T p.H743H Substitution - coding silent 11:607688-607688 + T22 COSM5341630 c.1344T>A p.L448L Substitution - coding silent 11:605617-605617 + LC_C15 COSM1188108 c.3154C>T p.R1052W Substitution - Missense 11:608613-608613 + CHOL26 COSM1744089 c.2212C>T p.R738W Substitution - Missense 11:607671-607671 + BD72T COSM4714181 c.3526C>T p.R1176W Substitution - Missense 11:608985-608985 + Au3 COSM5602075 c.4631C>T p.T1544I Substitution - Missense 11:610718-610718 + T3527 COSM4714167 c.80C>T p.P27L Substitution - Missense 11:581592-581592 + HCC4 COSM1604854 c.3594G>T p.R1198S Substitution - Missense 11:609053-609053 + 462 COSM4436710 c.4363C>T p.P1455S Substitution - Missense 11:610297-610297 + TCGA-BR-6452-01 COSM4034314 c.574A>G p.S192G Substitution - Missense 11:592628-592628 + AOCS-139-6-3 COSM3980474 c.1913C>A p.T638N Substitution - Missense 11:607372-607372 + PT24_2 COSM5904606 c.1777C>T p.R593C Substitution - Missense 11:607236-607236 + TCGA-BR-4292-01 COSM4034379 c.940G>A p.E314K Substitution - Missense 11:598418-598418 + 0008_CRUK_PC_0008_T1_DNA COSM3849506 c.1423G>A p.A475T Substitution - Missense 11:605696-605696 + TCGA-D7-8575-01 COSM4034559 c.3560G>A p.R1187Q Substitution - Missense 11:609019-609019 + SC_9008 COSM5561542 c.4043C>T p.P1348L Substitution - Missense 11:609502-609502 + TCGA-41-2572-01 COSM3747889 c.1703C>A p.P568Q Substitution - Missense 11:607162-607162 + HT115 COSM2036785 c.1625G>A p.R542Q Substitution - Missense 11:607084-607084 + TCGA-KK-A59Y-01 COSM4877941 c.2554G>A p.G852S Substitution - Missense 11:608013-608013 + HCC159 COSM3666444 c.703G>T p.V235F Substitution - Missense 11:597005-597005 + ESO-859 COSM1239824 c.1062G>A p.P354P Substitution - coding silent 11:601611-601611 + pfg072T COSM4748330 c.1034A>G p.K345R Substitution - Missense 11:601583-601583 + PCSI_0284_Pa_P_526 COSM2037061 c.3431G>A p.R1144Q Substitution - Missense 11:608890-608890 + TCGA-BR-8368-01 COSM1475606 c.1272G>A p.A424A Substitution - coding silent 11:605238-605238 + ESO-0459 COSM1262123 c.811C>T p.R271W Substitution - Missense 11:597487-597487 + TCGA-D1-A17Q-01 COSM928939 c.409G>A p.E137K Substitution - Missense 11:587453-587453 + TCGA-A1-A0SI-01 COSM3809729 c.3532C>T p.R1178W Substitution - Missense 11:608991-608991 + PT34 COSM5910760 c.2639C>T p.S880F Substitution - Missense 11:608098-608098 + TCGA-CM-6171-01 COSM1355070 c.1935G>A p.A645A Substitution - coding silent 11:607394-607394 + CAL33 COSM2036827 c.1781C>T p.T594I Substitution - Missense 11:607240-607240 + TCGA-BR-4361-01 COSM4034554 c.3426C>T p.H1142H Substitution - coding silent 11:608885-608885 + PTC-7C COSM3998512 c.3894G>A p.P1298P Substitution - coding silent 11:609353-609353 + sysucc-880T COSM5462037 c.927G>A p.L309L Substitution - coding silent 11:598405-598405 + TCGA-EE-A3JA-06 COSM3450652 c.3460C>T p.P1154S Substitution - Missense 11:608919-608919 + TCGA-66-2785-01 COSM689439 c.1073C>G p.S358C Substitution - Missense 11:601622-601622 + TCGA-G4-6628-01 COSM1355072 c.2003C>A p.P668Q Substitution - Missense 11:607462-607462 + 408 COSM4430358 c.3557C>T p.T1186I Substitution - Missense 11:609016-609016 + TCGA-ER-A3PL-06 COSM3450163 c.385T>G p.Y129D Substitution - Missense 11:587429-587429 + HCT15 COSM2036152 c.1057A>G p.T353A Substitution - Missense 11:601606-601606 + 0085_CRUK_PC_0085_T1_DNA COSM5421315 c.4119G>A p.A1373A Substitution - coding silent 11:609578-609578 + TCGA-D9-A6EC-06 COSM4400976 c.4790A>G p.K1597R Substitution - Missense 11:611069-611069 + TCGA-BR-4370-01 COSM4034561 c.3789C>T p.S1263S Substitution - coding silent 11:609248-609248 + sysucc-311T COSM5477696 c.340G>A p.A114T Substitution - Missense 11:587384-587384 + TCGA-EB-A3Y7-01 COSM3450657 c.3663C>T p.A1221A Substitution - coding silent 11:609122-609122 + CHC2113T COSM4788341 c.1203G>T p.R401S Substitution - Missense 11:605169-605169 + PT23_2 COSM5903797 c.2552C>T p.P851L Substitution - Missense 11:608011-608011 + TCGA-AZ-4615-01 COSM429386 c.3044_3055del12 p.G1019_S1022delGTRS Deletion - In frame 11:608503-608514 + TCGA-EE-A2MR-06 COSM3450517 c.1179C>T p.I393I Substitution - coding silent 11:605145-605145 + TCGA-DU-7015-01 COSM3967675 c.3096G>A p.A1032A Substitution - coding silent 11:608555-608555 + ccRCC-59 COSM1659718 c.1357C>T p.L453F Substitution - Missense 11:605630-605630 + S00938 COSM5663215 c.120G>A p.G40G Substitution - coding silent 11:581987-581987 + TARGET-30-PAPWFY COSM1287119 c.977A>G p.Q326R Substitution - Missense 11:598455-598455 + HCC77T COSM1604809 c.542A>G p.E181G Substitution - Missense 11:592596-592596 + BZ30 COSM4427079 c.1469C>T p.A490V Substitution - Missense 11:606459-606459 + OSCC-GB_00060111 COSM3710201 c.1133G>T p.R378I Substitution - Missense 11:601682-601682 + HCC89 COSM1604856 c.3902A>G p.D1301G Substitution - Missense 11:609361-609361 + CRC-06T COSM5456150 c.4679T>C p.M1560T Substitution - Missense 11:610958-610958 + AOCS-064-3-3 COSM3980461 c.912C>T p.L304L Substitution - coding silent 11:598390-598390 + ESO-114 COSM1262125 c.2546C>T p.S849F Substitution - Missense 11:608005-608005 + sysucc-1370T COSM5469667 c.543G>T p.E181D Substitution - Missense 11:592597-592597 + TCGA-G3-A25V-01 COSM4914612 c.4873A>G p.K1625E Substitution - Missense 11:611703-611703 + 46M COSM5588634 c.1031G>A p.R344Q Substitution - Missense 11:601580-601580 + TCGA-AA-3713-01 COSM5826989 c.981delC p.L329fs*1 Deletion - Frameshift 11:598459-598459 + TCGA-EI-6882-01 COSM3416050 c.3271C>T p.R1091W Substitution - Missense 11:608730-608730 + HCC167T COSM3666463 c.4358C>T p.P1453L Substitution - Missense 11:610292-610292 + SJDES014-R2 COSM4574499 c.68G>T p.G23V Substitution - Missense 11:581580-581580 + TCGA-DS-A1OC-01 COSM1293418 c.3826G>T p.D1276Y Substitution - Missense 11:609285-609285 + TCGA-KR-A7K7-01 COSM4922830 c.4442C>T p.P1481L Substitution - Missense 11:610529-610529 + 1517_CLM COSM5753735 c.1436C>T p.S479F Substitution - Missense 11:605709-605709 + TCGA-18-3406-01 COSM689321 c.4862C>G p.A1621G Substitution - Missense 11:611692-611692 + 587342 COSM1220479 c.1265T>C p.L422P Substitution - Missense 11:605231-605231 + TCGA-AU-6004-01 COSM429390 c.3609G>A p.A1203A Substitution - coding silent 11:609068-609068 + TCGA-DR-A0ZM-01 COSM458500 c.1893C>T p.F631F Substitution - coding silent 11:607352-607352 + TCGA-ER-A2NC-06 COSM2035862 c.749C>T p.S250F Substitution - Missense 11:597425-597425 + BCM683T COSM4799332 c.2229C>T p.H743H Substitution - coding silent 11:607688-607688 + KPOPBR-60-T COSM5963754 c.345C>T p.F115F Substitution - coding silent 11:587389-587389 + TCGA-CC-A7IG-01 COSM4943015 c.3676C>G p.H1226D Substitution - Missense 11:609135-609135 + U2940 COSM5621506 c.2992T>C p.S998P Substitution - Missense 11:608451-608451 + RKO COSM2037104 c.3628C>T p.P1210S Substitution - Missense 11:609087-609087 + TCGA-KK-A59V-01 COSM4878329 c.1837C>A p.R613R Substitution - coding silent 11:607296-607296 + 2492722 COSM5721616 c.2982C>T p.S994S Substitution - coding silent 11:608441-608441 + SNU-C2B COSM2035486 c.602G>A p.C201Y Substitution - Missense 11:592656-592656 + EGC15 COSM2036847 c.2064C>T p.D688D Substitution - coding silent 11:607523-607523 + TCGA-02-0055-01 COSM3397964 c.2921A>T p.D974V Substitution - Missense 11:608380-608380 + HCC57T COSM1604859 c.4414-8C>T p.? Unknown 11:610493-610493 + 6T COSM3710201 c.1133G>T p.R378I Substitution - Missense 11:601682-601682 + HCC017T COSM5815015 c.2455A>T p.K819* Substitution - Nonsense 11:607914-607914 + sysucc-783T COSM2036428 c.1187C>T p.T396M Substitution - Missense 11:605153-605153 + TCGA-ER-A2NC-06 COSM3450618 c.1985C>T p.P662L Substitution - Missense 11:607444-607444 + CSCC-29-T COSM4480695 c.2442C>T p.P814P Substitution - coding silent 11:607901-607901 + TCGA-B0-4833-01 COSM3359268 c.4799A>C p.Q1600P Substitution - Missense 11:611078-611078 + LUAD-CHTN-MAD06-00668 COSM358473 c.1424C>A p.A475D Substitution - Missense 11:605697-605697 + SNU-175 COSM2036602 c.1591A>G p.S531G Substitution - Missense 11:606581-606581 + TCGA-EP-A26S-01 COSM4913471 c.3984A>G p.E1328E Substitution - coding silent 11:609443-609443 + Pat_74_A COSM5838953 c.2416G>T p.E806* Substitution - Nonsense 11:607875-607875 + TCGA-D1-A0ZO-01 COSM929313 c.1578C>T p.R526R Substitution - coding silent 11:606568-606568 + LIM2405 COSM4613263 c.3261_3266delGTCCCG p.R1091_S1092delRS Deletion - In frame 11:608720-608725 + J13_T COSM3953540 c.1667G>T p.G556V Substitution - Missense 11:607126-607126 + TCGA-DD-A3A9-01 COSM4920748 c.4872C>A p.D1624E Substitution - Missense 11:611702-611702 + TCGA-GC-A3RC-01 COSM3791652 c.3365G>A p.C1122Y Substitution - Missense 11:608824-608824 + CSCC-31-T COSM4490487 c.3647C>T p.P1216L Substitution - Missense 11:609106-609106 + HCC4T COSM1604854 c.3594G>T p.R1198S Substitution - Missense 11:609053-609053 + TCGA-G4-6309-01 COSM1355052 c.1437C>T p.S479S Substitution - coding silent 11:605710-605710 + TCGA-BC-A10Y-01 COSM2036988 c.2840C>T p.S947F Substitution - Missense 11:608299-608299 + CSCC-31-T COSM4516944 c.2550_2551CC>TT p.P851S Substitution - Missense 11:608009-608010 + T11 COSM3998512 c.3894G>A p.P1298P Substitution - coding silent 11:609353-609353 + LUAD-YINHD COSM348474 c.261G>T p.A87A Substitution - coding silent 11:587305-587305 + BD216T COSM3666442 c.662C>T p.P221L Substitution - Missense 11:596964-596964 + Au10 COSM4402337 c.2307C>T p.V769V Substitution - coding silent 11:607766-607766 + TCGA-EE-A2ML-06 COSM3450224 c.431C>T p.S144F Substitution - Missense 11:591394-591394 + OSCC-GB_01210111 COSM5955033 c.3887C>T p.S1296F Substitution - Missense 11:609346-609346 + TCGA-CG-5726-01 COSM4034372 c.696G>A p.A232A Substitution - coding silent 11:596998-596998 + TCGA-AX-A06H-01 COSM928849 c.183G>A p.A61A Substitution - coding silent 11:582050-582050 + sysucc-882T COSM5446932 c.3119G>A p.R1040H Substitution - Missense 11:608578-608578 + TCGA-C5-A1BL-01 COSM4837111 c.4714G>A p.E1572K Substitution - Missense 11:610993-610993 + DLD1 COSM4622202 c.2473C>T p.R825W Substitution - Missense 11:607932-607932 + H522 COSM1197017 c.1724A>G p.N575S Substitution - Missense 11:607183-607183 + TCGA-66-2793-01 COSM689354 c.2776G>T p.G926C Substitution - Missense 11:608235-608235 + PT46 COSM5929336 c.367C>T p.P123S Substitution - Missense 11:587411-587411 + TCGA-DK-A1AC-01 COSM1298254 c.838G>A p.E280K Substitution - Missense 11:597514-597514 + 480 COSM4439097 c.1949G>T p.S650I Substitution - Missense 11:607408-607408 + HCC77 COSM1604809 c.542A>G p.E181G Substitution - Missense 11:592596-592596 + TCGA-EE-A2MG-06 COSM3450159 c.219C>T p.S73S Substitution - coding silent 11:587263-587263 + C0050T COSM4165867 c.3511G>C p.A1171P Substitution - Missense 11:608970-608970 + TCGA-A2-A0T3-01 COSM429380 c.2394G>C p.T798T Substitution - coding silent 11:607853-607853 + RK091_C01 COSM1628116 c.3352C>T p.R1118W Substitution - Missense 11:608811-608811 + Pat_74_B COSM5838953 c.2416G>T p.E806* Substitution - Nonsense 11:607875-607875 + TCGA-BR-8081-01 COSM4034381 c.1009C>T p.R337W Substitution - Missense 11:598487-598487 + TCGA-DC-6157-01 COSM1561319 c.4094C>T p.A1365V Substitution - Missense 11:609553-609553 + TCGA-CD-A4MG-01 COSM1355070 c.1935G>A p.A645A Substitution - coding silent 11:607394-607394 + LUAD-CHTN-Z4716A COSM361531 c.2168G>T p.G723V Substitution - Missense 11:607627-607627 + TCGA-B5-A0JY-01 COSM929014 c.446G>A p.R149Q Substitution - Missense 11:591409-591409 + SW403 COSM4655189 c.1751G>T p.C584F Substitution - Missense 11:607210-607210 + TCGA-B5-A11E-01 COSM929341 c.1972C>T p.R658C Substitution - Missense 11:607431-607431 + S00501 COSM5621506 c.2992T>C p.S998P Substitution - Missense 11:608451-608451 + T3724 COSM4714187 c.4929G>A p.T1643T Substitution - coding silent 11:611759-611759 + CHC1756T COSM4804512 c.1605G>T p.A535A Substitution - coding silent 11:606595-606595 + NCI-H716 COSM4646972 c.3892C>G p.P1298A Substitution - Missense 11:609351-609351 + AOCS-064-1-6 COSM3980461 c.912C>T p.L304L Substitution - coding silent 11:598390-598390 + T3203 COSM4714169 c.532_534delGAG p.E181delE Deletion - In frame 11:592586-592588 + HCT15 COSM4622200 c.2154C>A p.G718G Substitution - coding silent 11:607613-607613 + RKO COSM2035847 c.695C>T p.A232V Substitution - Missense 11:596997-596997 + TCGA-EE-A2MS-06 COSM3450161 c.357C>A p.A119A Substitution - coding silent 11:587401-587401 + TCGA-CW-5589-01 COSM467083 c.3363G>A p.E1121E Substitution - coding silent 11:608822-608822 + T3262 COSM2037085 c.3470G>A p.R1157Q Substitution - Missense 11:608929-608929 + ESCC_BICR_053T COSM5442053 c.3515G>A p.R1172Q Substitution - Missense 11:608974-608974 + 2492729 COSM5725757 c.2690C>T p.P897L Substitution - Missense 11:608149-608149 + TCGA-FU-A3HY-01 COSM4838531 c.1289C>G p.S430C Substitution - Missense 11:605255-605255 + TCGA-BR-6452-01 COSM4034375 c.916T>A p.S306T Substitution - Missense 11:598394-598394 + TCGA-CA-6717-01 COSM1354935 c.472C>A p.R158R Substitution - coding silent 11:591435-591435 + TCGA-41-2573-01 COSM3397962 c.2809C>T p.P937S Substitution - Missense 11:608268-608268 + 2492721 COSM5721616 c.2982C>T p.S994S Substitution - coding silent 11:608441-608441 + HCC89T COSM1604856 c.3902A>G p.D1301G Substitution - Missense 11:609361-609361 + C008 COSM5523462 c.2253C>T p.A751A Substitution - coding silent 11:607712-607712 + S00941 COSM5663622 c.2630G>C p.C877S Substitution - Missense 11:608089-608089 + 353 COSM3723047 c.4688T>G p.L1563R Substitution - Missense 11:610967-610967 + S02248 COSM5679409 c.4932G>A p.Q1644Q Substitution - coding silent 11:611762-611762 + CSCC-20-T COSM4509099 c.796C>T p.R266* Substitution - Nonsense 11:597472-597472 + TCGA-AZ-4315-01 COSM1355020 c.1116A>G p.Q372Q Substitution - coding silent 11:601665-601665 + TCGA-DR-A0ZM-01 COSM458504 c.1590C>G p.L530L Substitution - coding silent 11:606580-606580 + PD11367a COSM5773061 c.4195G>C p.V1399L Substitution - Missense 11:609654-609654 + PTC-73C COSM4145958 c.3134G>A p.R1045Q Substitution - Missense 11:608593-608593 + PT50 COSM5937507 c.4675-8C>T p.? Unknown 11:610946-610946 + CHEWS002 COSM4574519 c.951G>A p.A317A Substitution - coding silent 11:598429-598429 + TCGA-BR-6565-01 COSM4034523 c.1805A>G p.D602G Substitution - Missense 11:607264-607264 + ESCC_139 COSM5643199 c.2478C>T p.S826S Substitution - coding silent 11:607937-607937 + HX13T COSM1604854 c.3594G>T p.R1198S Substitution - Missense 11:609053-609053 + 345973 COSM3726571 c.2212C>G p.R738G Substitution - Missense 11:607671-607671 + TCGA-G4-6315-01 COSM1355047 c.1204C>A p.P402T Substitution - Missense 11:605170-605170 + TCGA-JW-A5VL-01 COSM4846646 c.436C>G p.P146A Substitution - Missense 11:591399-591399 + TARGET-30-PARDIW COSM1287121 c.2479G>A p.E827K Substitution - Missense 11:607938-607938 + HCT8 COSM4622205 c.4442C>A p.P1481Q Substitution - Missense 11:610529-610529 + TCGA-G4-6588-01 COSM1355082 c.3405G>A p.K1135K Substitution - coding silent 11:608864-608864 + CRC-03T COSM4877941 c.2554G>A p.G852S Substitution - Missense 11:608013-608013 + CHEWS026 COSM4574547 c.3007A>G p.K1003E Substitution - Missense 11:608466-608466 + ESCC_BICR_051T COSM5443950 c.2741C>G p.S914C Substitution - Missense 11:608200-608200 + ESCC_BICR_051T COSM5443948 c.1590C>T p.L530L Substitution - coding silent 11:606580-606580 + TCGA-FW-A3R5-06 COSM3869697 c.3992C>T p.S1331L Substitution - Missense 11:609451-609451 + T3152 COSM4714185 c.4653G>A p.A1551A Substitution - coding silent 11:610740-610740 + C058 COSM5525422 c.2685C>T p.L895L Substitution - coding silent 11:608144-608144 + TCGA-ER-A198-06 COSM3450648 c.3427G>A p.E1143K Substitution - Missense 11:608886-608886 + CHC2113T COSM4788341 c.1203G>T p.R401S Substitution - Missense 11:605169-605169 + TCGA-AC-A5XS-01 COSM1287121 c.2479G>A p.E827K Substitution - Missense 11:607938-607938 + S02209 COSM5675098 c.2479G>T p.E827* Substitution - Nonsense 11:607938-607938 + TCGA-BR-6452-01 COSM4034182 c.173A>G p.D58G Substitution - Missense 11:582040-582040 + sysucc-311T COSM5477717 c.1175G>A p.R392Q Substitution - Missense 11:605141-605141 + EWS834 COSM4574543 c.1791G>A p.A597A Substitution - coding silent 11:607250-607250 + TCGA-66-2782-01 COSM689350 c.3369C>T p.S1123S Substitution - coding silent 11:608828-608828 + ESO-859 COSM1239828 c.3318_3320delGAA p.K1110delK Deletion - In frame 11:608777-608779 + TCGA-AY-6197-01 COSM1355101 c.4169delC p.L1392fs*8 Deletion - Frameshift 11:609628-609628 + CPCG0268-F1 COSM4881048 c.421-7C>T p.? Unknown 11:591377-591377 + ESCC_134 COSM5642675 c.2398C>T p.R800W Substitution - Missense 11:607857-607857 + TCGA-G4-6586-01 COSM1354944 c.512T>C p.V171A Substitution - Missense 11:592566-592566 + TCGA-AX-A05Z-01 COSM929213 c.1120C>T p.R374* Substitution - Nonsense 11:601669-601669 + TCGA-E9-A1R7-01 COSM1475606 c.1272G>A p.A424A Substitution - coding silent 11:605238-605238 + PDA_086 COSM5002817 c.2084C>T p.A695V Substitution - Missense 11:607543-607543 + CCC1T COSM3666442 c.662C>T p.P221L Substitution - Missense 11:596964-596964 + TCGA-BR-6565-01 COSM4034377 c.935C>T p.A312V Substitution - Missense 11:598413-598413 + TCGA-BR-8487-01 COSM4034545 c.2464A>G p.K822E Substitution - Missense 11:607923-607923 + HCT8 COSM4622200 c.2154C>A p.G718G Substitution - coding silent 11:607613-607613 + SC_9109 COSM5556139 c.2717G>A p.G906D Substitution - Missense 11:608176-608176 + CRC-19T COSM5480899 c.1647A>G p.R549R Substitution - coding silent 11:607106-607106 + Pat_41_B COSM5838909 c.848G>A p.R283K Substitution - Missense 11:597524-597524 + CSCC-44-T COSM4483306 c.268C>T p.Q90* Substitution - Nonsense 11:587312-587312 + YUOMEGA COSM5372990 c.3998C>T p.P1333L Substitution - Missense 11:609457-609457 + PTC-6C COSM5446640 c.3056_3067del12 p.G1019_S1022delGTRS Deletion - In frame 11:608515-608526 + UM-SCC-2 COSM4599362 c.3610C>T p.P1204S Substitution - Missense 11:609069-609069 + TCGA-BR-8077-01 COSM4034413 c.1080A>T p.K360N Substitution - Missense 11:601629-601629 + TCGA-D1-A167-01 COSM929345 c.2039G>T p.R680M Substitution - Missense 11:607498-607498 + TCGA-G4-6320-01 COSM3687400 c.234C>T p.D78D Substitution - coding silent 11:587278-587278 + TCGA-BP-5180-01 COSM467081 c.2808C>A p.P936P Substitution - coding silent 11:608267-608267 + CSCC-27-T COSM4494906 c.4424C>T p.P1475L Substitution - Missense 11:610511-610511 + PTC-7C COSM429376 c.1716G>A p.P572P Substitution - coding silent 11:607175-607175 + STC252 COSM5050942 c.3798C>T p.A1266A Substitution - coding silent 11:609257-609257 + CHC059T COSM4803088 c.3650C>G p.T1217S Substitution - Missense 11:609109-609109 + BD236T COSM5519009 c.341C>T p.A114V Substitution - Missense 11:587385-587385 + YUGATOR COSM4509099 c.796C>T p.R266* Substitution - Nonsense 11:597472-597472 + TCGA-AH-6644-01 COSM3416048 c.2520C>T p.S840S Substitution - coding silent 11:607979-607979 + S0004 COSM5882096 c.4454C>G p.S1485* Substitution - Nonsense 11:610541-610541 + TCGA-BT-A20V-01 COSM415511 c.3939G>A p.L1313L Substitution - coding silent 11:609398-609398 + ESCC_134 COSM5642673 c.2397C>G p.F799L Substitution - Missense 11:607856-607856 + HCC097T COSM5816432 c.382C>A p.H128N Substitution - Missense 11:587426-587426 + pfg212T COSM4748332 c.4433C>T p.P1478L Substitution - Missense 11:610520-610520 + 2492723 COSM5721616 c.2982C>T p.S994S Substitution - coding silent 11:608441-608441 + TCGA-DD-A73G-01 COSM4941272 c.1513C>T p.L505L Substitution - coding silent 11:606503-606503 + ATL071 COSM5704094 c.1394G>A p.R465Q Substitution - Missense 11:605667-605667 + Pat_44_B COSM1239826 c.2078G>A p.R693Q Substitution - Missense 11:607537-607537 + TCGA-43-6770-01 COSM689352 c.3050G>T p.R1017L Substitution - Missense 11:608509-608509 + TCGA-D1-A174-01 COSM929396 c.4237G>A p.A1413T Substitution - Missense 11:609696-609696 + TCGA-AY-6197-01 COSM5136312 c.4238delC p.A1415fs*94 Deletion - Frameshift 11:609697-609697 + TCGA-AP-A0LH-01 COSM929370 c.2605_2606insT p.A869fs*47 Insertion - Frameshift 11:608064-608065 + C106 COSM4616163 c.4791G>A p.K1597K Substitution - coding silent 11:611070-611070 + AOCS-139-1-5 COSM3980474 c.1913C>A p.T638N Substitution - Missense 11:607372-607372 + T3024 COSM4714179 c.2944_2945delAG p.R982fs*41 Deletion - Frameshift 11:608403-608404 + DLD1 COSM4622205 c.4442C>A p.P1481Q Substitution - Missense 11:610529-610529 + SH-0622 COSM5017342 c.2803_2804insC p.E938fs*5 Insertion - Frameshift 11:608262-608263 + NB-1375 COSM1287123 c.3040G>A p.G1014R Substitution - Missense 11:608499-608499 + TCGA-HU-A4GQ-01 COSM4034563 c.3842A>T p.Q1281L Substitution - Missense 11:609301-609301 + Pat_06_A COSM5838907 c.715G>A p.A239T Substitution - Missense 11:597017-597017 + TCGA-RC-A7SF-01 COSM4923137 c.600C>G p.L200L Substitution - coding silent 11:592654-592654 + PT08_1 COSM5893601 c.621-7C>T p.? Unknown 11:596916-596916 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.325838 11p15.5 611780

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.Q1600P c.4799A>C 11 611078 RCCC A G IntronicSNV . c.420+134A>G 11 587598 HC A G Missense p.D602G c.1805A>G 11 607264 STAD A G Missense p.Q326R c.977A>G 11 598455 NB A G Synonymous p.P146P c.438A>G 11 591401 HNSC A T Missense p.D974V c.2921A>T 11 608380 GBM A T Missense p.I1577F c.4729A>T 11 611008 HNSC A T Missense p.S1607C c.4819A>T 11 611649 MM C A Missense p.A910D c.2729C>A 11 608188 BRCA C A Missense p.P1360T c.4078C>A 11 609537 LUAD C A Missense p.P568Q c.1703C>A 11 607162 GBM C A Synonymous p.A119A c.357C>A 11 587401 CM C A Synonymous p.P936P c.2808C>A 11 608267 RCCC CC TT Missense p.A1266V c.3797_3798delinsTT 11 609256 CM CC TT Missense p.P354S c.1059_1060delinsTT 11 601608 CM CC TT Missense p.R1089W c.3264_3265delinsTT 11 608723 CM CC TT Synonymous p.(=) c.3936_3937delinsTT 11 609395 CM C G Missense p.A1621G c.4862C>G 11 611692 LUSC C G Missense p.I818M c.2454C>G 11 607913 LUAD C G Missense p.L433V c.1297C>G 11 605263 HNSC C G Missense p.S101C c.302C>G 11 587346 HNSC C G Missense p.S1372C c.4115C>G 11 609574 HNSC C G Missense p.S510W c.1529C>G 11 606519 HNSC C T IntronicSNV . c.505-112C>T 11 592447 CM C T IntronicSNV . c.95-12C>T 11 581950 CM C T Missense p.A1621V c.4862C>T 11 611692 HNSC C T Missense p.A312V c.935C>T 11 598413 STAD C T Missense p.A645V c.1934C>T 11 607393 GBM C T Missense p.A645V c.1934C>T 11 607393 LUAD C T Missense p.P1154S c.3460C>T 11 608919 CM C T Missense p.P183L c.548C>T 11 592602 COREAD C T Missense p.P662L c.1985C>T 11 607444 CM C T Missense p.P937S c.2809C>T 11 608268 GBM C T Missense p.S144F c.431C>T 11 591394 CM C T Missense p.S250F c.749C>T 11 597425 CM C T Missense p.S754F c.2261C>T 11 607720 CM C T Missense p.S813L c.2438C>T 11 607897 HNSC C T Missense p.S849F c.2546C>T 11 608005 ESCA C T Nonsense p.R158* c.472C>T 11 591435 CM C T Synonymous p.D1235D c.3705C>T 11 609164 CM C T Synonymous p.D1593D c.4779C>T 11 611058 BRCA C T Synonymous p.F1302F c.3906C>T 11 609365 CM C T Synonymous p.F554F c.1662C>T 11 607121 CM C T Synonymous p.P1242P c.3726C>T 11 609185 CM C T Synonymous p.R526R c.1578C>T 11 606568 UCEC C T Synonymous p.S1123S c.3369C>T 11 608828 LUSC C T Synonymous p.S1263S c.3789C>T 11 609248 STAD C T Synonymous p.S464S c.1392C>T 11 605665 CM C T Synonymous p.S73S c.219C>T 11 587263 CM C T Synonymous p.S747S c.2241C>T 11 607700 CM GAA - InFrameDeletion p.K1110delK c.3327_3329delGAA 11 608777 ESCA G A Missense p.A1413T c.4237G>A 11 609696 UCEC G A Missense p.C134Y c.401G>A 11 587445 THCA G A Missense p.D103N c.307G>A 11 587351 HNSC G A Missense p.D1276N c.3826G>A 11 609285 UCEC G A Missense p.E1143K c.3427G>A 11 608886 CM G A Missense p.E137K c.409G>A 11 587453 HNSC G A Missense p.E314K c.940G>A 11 598418 STAD G A Missense p.E827K c.2479G>A 11 607938 NB G A Missense p.E847K c.2539G>A 11 607998 LUSC G A Missense p.G1014R c.3040G>A 11 608499 NB G A Missense p.G852S c.2554G>A 11 608013 PRAD G A Missense p.R613Q c.1838G>A 11 607297 BLCA G A Missense p.R993H c.2978G>A 11 608437 STAD G A Synonymous p.A232A c.696G>A 11 596998 STAD G A Synonymous p.A424A c.1272G>A 11 605238 BRCA G A Synonymous p.A595A c.1785G>A 11 607244 HNSC G A Synonymous p.A61A c.183G>A 11 582050 UCEC G A Synonymous p.E1121E c.3363G>A 11 608822 RCCC G A Synonymous p.E857E c.2571G>A 11 608030 STAD G A Synonymous p.L1313L c.3939G>A 11 609398 BLCA G A Synonymous p.L422L c.1266G>A 11 605232 HNSC G A Synonymous p.P354P c.1062G>A 11 601611 BRCA G A Synonymous p.P354P c.1062G>A 11 601611 ESCA G A Synonymous p.R1130R c.3390G>A 11 608849 UCEC G A Synonymous p.T871T c.2613G>A 11 608072 THCA G C Missense p.A119P c.355G>C 11 587399 LUAD G C Missense p.R957P c.2870G>C 11 608329 LUAD G C Synonymous p.T798T c.2394G>C 11 607853 BRCA GGA - InFrameDeletion p.E1572delE c.4715_4717delAGG 11 610989 BRCA G T Missense p.A127S c.379G>T 11 587423 PAAD G T Missense p.A900S c.2698G>T 11 608157 LUAD G T Missense p.D193Y c.577G>T 11 592631 HNSC G T Missense p.G926C c.2776G>T 11 608235 LUSC G T Missense p.K1556N c.4668G>T 11 610755 CM G T Missense p.R1017L c.3050G>T 11 608509 LUSC G T Missense p.R1091L c.3272G>T 11 608731 HNSC G T Nonsense p.G553* c.1657G>T 11 607116 HC G T Synonymous p.A424A c.1272G>T 11 605238 CM G T Synonymous p.L504L c.1512G>T 11 606502 OV T C Synonymous p.L1324L c.3970T>C 11 609429 MB - T Frameshift p.Q870Pfs*46 c.2606_2607insT 11 608065 UCEC