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 23 53561133 53561133 + Missense_Mutation SNP C C T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:53561133C>T c.12857G>A c.(12856-12858)cGt>cAt p.R4286H ACC 23 53591626 53591626 + Missense_Mutation SNP A A C TCGA-OR-A5K5-01A-11D-A29I-10 TCGA-OR-A5K5-10A-01D-A29L-10 g.chrX:53591626A>C c.6938T>G c.(6937-6939)gTg>gGg p.V2313G ACC 23 53602737 53602737 + Missense_Mutation SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:53602737C>A c.5896G>T c.(5896-5898)Gat>Tat p.D1966Y ACC 23 53607986 53607986 + Splice_Site SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chrX:53607986C>A c.5521G>T c.(5521-5523)Gtt>Ttt p.V1841F ACC 23 53616611 53616611 + Missense_Mutation SNP C C T TCGA-OR-A5J4-01A-11D-A29I-10 TCGA-OR-A5J4-10A-01D-A29L-10 g.chrX:53616611C>T c.4357G>A c.(4357-4359)Gag>Aag p.E1453K ACC 23 53634661 53634661 + Splice_Site SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:53634661C>A c.e24-1 BLCA 23 53561612 53561612 + Silent SNP C C T TCGA-E7-A5KE-01A-11D-A289-08 TCGA-E7-A5KE-10A-01D-A289-08 g.chrX:53561612C>T c.12696G>A c.(12694-12696)gaG>gaA p.E4232E BLCA 23 53564591 53564591 + Silent SNP G G C TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chrX:53564591G>C c.12063C>G c.(12061-12063)gtC>gtG p.V4021V BLCA 23 53564649 53564649 + Missense_Mutation SNP C C A TCGA-XF-A9SX-01A-21D-A391-08 TCGA-XF-A9SX-10A-01D-A394-08 g.chrX:53564649C>A c.12005G>T c.(12004-12006)cGc>cTc p.R4002L BLCA 23 53565383 53565383 + Missense_Mutation SNP G G A TCGA-HQ-A2OF-01A-11D-A26M-08 TCGA-HQ-A2OF-10B-01D-A26K-08 g.chrX:53565383G>A c.11911C>T c.(11911-11913)Cgg>Tgg p.R3971W BLCA 23 53574783 53574785 + In_Frame_Del DEL GTG GTG - TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chrX:53574783_53574785delGTG c.10485_10487delCAC c.(10483-10488)accact>act p.3495_3496TT>T BLCA 23 53574942 53574942 + Missense_Mutation SNP A A G TCGA-GD-A76B-01A-11D-A32B-08 TCGA-GD-A76B-10A-01D-A329-08 g.chrX:53574942A>G c.10328T>C c.(10327-10329)aTc>aCc p.I3443T BLCA 23 53575134 53575134 + Missense_Mutation SNP G G A TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chrX:53575134G>A c.10136C>T c.(10135-10137)tCc>tTc p.S3379F BLCA 23 53575138 53575138 + Nonsense_Mutation SNP G G A TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chrX:53575138G>A c.10132C>T c.(10132-10134)Cag>Tag p.Q3378* BLCA 23 53576080 53576080 + Missense_Mutation SNP G G A TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chrX:53576080G>A c.9875C>T c.(9874-9876)gCa>gTa p.A3292V BLCA 23 53577926 53577926 + Silent SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chrX:53577926G>C c.9321C>G c.(9319-9321)ctC>ctG p.L3107L BLCA 23 53578103 53578103 + Silent SNP C C T TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chrX:53578103C>T c.9144G>A c.(9142-9144)caG>caA p.Q3048Q BLCA 23 53578136 53578136 + Missense_Mutation SNP C C G TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chrX:53578136C>G c.9111G>C c.(9109-9111)caG>caC p.Q3037H BLCA 23 53578272 53578272 + Silent SNP C C G TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chrX:53578272C>G c.9051G>C c.(9049-9051)gtG>gtC p.V3017V BLCA 23 53587226 53587226 + Silent SNP C C T TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chrX:53587226C>T c.7659G>A c.(7657-7659)ctG>ctA p.L2553L BLCA 23 53592082 53592082 + Missense_Mutation SNP C C T TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chrX:53592082C>T c.6826G>A c.(6826-6828)Gag>Aag p.E2276K BLCA 23 53595718 53595718 + Missense_Mutation SNP C C T TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chrX:53595718C>T c.6641G>A c.(6640-6642)cGg>cAg p.R2214Q BLCA 23 53602629 53602629 + Missense_Mutation SNP C C T TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chrX:53602629C>T c.6004G>A c.(6004-6006)Gat>Aat p.D2002N BLCA 23 53602710 53602710 + Missense_Mutation SNP C C G TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chrX:53602710C>G c.5923G>C c.(5923-5925)Gag>Cag p.E1975Q BLCA 23 53602723 53602723 + Silent SNP C C T TCGA-FD-A5BZ-01A-11D-A289-08 TCGA-FD-A5BZ-10A-01D-A289-08 g.chrX:53602723C>T c.5910G>A c.(5908-5910)ggG>ggA p.G1970G BLCA 23 53603879 53603879 + Silent SNP T T C TCGA-C4-A0F6-01A-11D-A10S-08 TCGA-C4-A0F6-10A-01D-A10S-08 g.chrX:53603879T>C c.5865A>G c.(5863-5865)gcA>gcG p.A1955A BLCA 23 53607868 53607868 + Missense_Mutation SNP C C G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chrX:53607868C>G c.5639G>C c.(5638-5640)cGc>cCc p.R1880P BLCA 23 53611145 53611145 + Splice_Site SNP C C T TCGA-XF-A9SZ-01A-11D-A391-08 TCGA-XF-A9SZ-10A-01D-A394-08 g.chrX:53611145C>T c.e40+1 BLCA 23 53611263 53611263 + Missense_Mutation SNP G G C TCGA-GC-A6I3-01A-11D-A31L-08 TCGA-GC-A6I3-10A-01D-A31J-08 g.chrX:53611263G>C c.5044C>G c.(5044-5046)Ctc>Gtc p.L1682V BLCA 23 53615408 53615408 + Silent SNP C C T TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chrX:53615408C>T c.4548G>A c.(4546-4548)caG>caA p.Q1516Q BLCA 23 53617425 53617425 + Missense_Mutation SNP C C G TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chrX:53617425C>G c.4130G>C c.(4129-4131)aGa>aCa p.R1377T BLCA 23 53619390 53619390 + Missense_Mutation SNP C C T TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chrX:53619390C>T c.3940G>A c.(3940-3942)Gaa>Aaa p.E1314K BLCA 23 53620499 53620499 + Nonsense_Mutation SNP G G C TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chrX:53620499G>C c.3566C>G c.(3565-3567)tCa>tGa p.S1189* BLCA 23 53620515 53620515 + Missense_Mutation SNP C C G TCGA-ZF-AA56-01A-31D-A391-08 TCGA-ZF-AA56-10A-01D-A394-08 g.chrX:53620515C>G c.3550G>C c.(3550-3552)Gag>Cag p.E1184Q BLCA 23 53621517 53621517 + Missense_Mutation SNP G G A TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chrX:53621517G>A c.3445C>T c.(3445-3447)Ccc>Tcc p.P1149S BLCA 23 53630453 53630453 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chrX:53630453G>A c.2752C>T c.(2752-2754)Cgt>Tgt p.R918C BLCA 23 53631583 53631583 + Missense_Mutation SNP G G C TCGA-CF-A27C-01A-11D-A16O-08 TCGA-CF-A27C-10A-01D-A16O-08 g.chrX:53631583G>C c.2709C>G c.(2707-2709)atC>atG p.I903M BLCA 23 53631594 53631594 + Missense_Mutation SNP G G A TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chrX:53631594G>A c.2698C>T c.(2698-2700)Cat>Tat p.H900Y BLCA 23 53634540 53634540 + Missense_Mutation SNP C C G TCGA-E7-A677-01A-11D-A30E-08 TCGA-E7-A677-10A-01D-A30H-08 g.chrX:53634540C>G c.2440G>C c.(2440-2442)Gac>Cac p.D814H BLCA 23 53654791 53654791 + Missense_Mutation SNP A A C TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chrX:53654791A>C c.1282T>G c.(1282-1284)Ttt>Gtt p.F428V BLCA 23 53655540 53655540 + Frame_Shift_Del DEL A A - TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chrX:53655540delA c.1146delT c.(1144-1146)tttfs p.F382fs BLCA 23 53672365 53672365 + Silent SNP G G A TCGA-BL-A3JM-01A-12D-A21A-08 TCGA-BL-A3JM-11A-31D-A21A-08 g.chrX:53672365G>A c.402C>T c.(400-402)gtC>gtT p.V134V BLCA 23 53674349 53674349 + Missense_Mutation SNP C C T TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chrX:53674349C>T c.313G>A c.(313-315)Gag>Aag p.E105K BRCA 23 53560294 53560294 + Silent SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:53560294G>A c.13101C>T c.(13099-13101)tgC>tgT p.C4367C BRCA 23 53560335 53560335 + Missense_Mutation SNP C C G TCGA-A8-A09I-01A-22W-A050-09 TCGA-A8-A09I-10A-01W-A055-09 g.chrX:53560335C>G c.13060G>C c.(13060-13062)Gag>Cag p.E4354Q BRCA 23 53561010 53561010 + Missense_Mutation SNP C C T TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chrX:53561010C>T c.12980G>A c.(12979-12981)cGa>cAa p.R4327Q BRCA 23 53561598 53561598 + Missense_Mutation SNP C C T TCGA-D8-A27P-01A-11D-A16D-09 TCGA-D8-A27P-10A-01D-A16D-09 g.chrX:53561598C>T c.12710G>A c.(12709-12711)cGc>cAc p.R4237H BRCA 23 53561637 53561637 + Missense_Mutation SNP G G A TCGA-A2-A3XY-01A-11D-A23C-09 TCGA-A2-A3XY-10A-01D-A23C-09 g.chrX:53561637G>A c.12671C>T c.(12670-12672)gCg>gTg p.A4224V BRCA 23 53562391 53562391 + Missense_Mutation SNP C C G TCGA-A8-A09I-01A-22W-A050-09 TCGA-A8-A09I-10A-01W-A055-09 g.chrX:53562391C>G c.12603G>C c.(12601-12603)gaG>gaC p.E4201D BRCA 23 53562452 53562452 + Missense_Mutation SNP A A C TCGA-E2-A1II-01A-11D-A142-09 TCGA-E2-A1II-10A-01D-A142-09 g.chrX:53562452A>C c.12542T>G c.(12541-12543)tTt>tGt p.F4181C BRCA 23 53563167 53563167 + Missense_Mutation SNP C C T TCGA-EW-A1PC-01B-11D-A21Q-09 TCGA-EW-A1PC-10A-01D-A21Q-09 g.chrX:53563167C>T c.12472G>A c.(12472-12474)Gtt>Att p.V4158I BRCA 23 53563526 53563526 + Missense_Mutation SNP C C G TCGA-B6-A0I6-01A-11D-A128-09 TCGA-B6-A0I6-10A-01W-A055-09 g.chrX:53563526C>G c.12240G>C c.(12238-12240)ttG>ttC p.L4080F BRCA 23 53565354 53565354 + Silent SNP C C A TCGA-A8-A09M-01A-11W-A019-09 TCGA-A8-A09M-10A-01W-A021-09 g.chrX:53565354C>A c.11940G>T c.(11938-11940)ggG>ggT p.G3980G BRCA 23 53566024 53566024 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:53566024C>T c.11650G>A c.(11650-11652)Gag>Aag p.E3884K BRCA 23 53570803 53570803 + Splice_Site SNP G G A TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chrX:53570803G>A c.11378C>T c.(11377-11379)aCg>aTg p.T3793M BRCA 23 53570824 53570824 + Missense_Mutation SNP C C T TCGA-A2-A0ER-01A-21W-A050-09 TCGA-A2-A0ER-10A-01W-A055-09 g.chrX:53570824C>T c.11357G>A c.(11356-11358)cGg>cAg p.R3786Q BRCA 23 53573461 53573461 + Silent SNP G G A TCGA-A8-A06Z-01A-11W-A019-09 TCGA-A8-A06Z-10A-01W-A021-09 g.chrX:53573461G>A c.10851C>T c.(10849-10851)gaC>gaT p.D3617D BRCA 23 53573667 53573667 + Missense_Mutation SNP C C G TCGA-A8-A06X-01A-21W-A019-09 TCGA-A8-A06X-10A-01W-A021-09 g.chrX:53573667C>G c.10756G>C c.(10756-10758)Gag>Cag p.E3586Q BRCA 23 53574688 53574688 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:53574688C>T c.10582G>A c.(10582-10584)Gta>Ata p.V3528I BRCA 23 53575140 53575140 + Nonsense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chrX:53575140G>C c.10130C>G c.(10129-10131)tCa>tGa p.S3377* BRCA 23 53575991 53575991 + Missense_Mutation SNP C C T TCGA-A2-A3XT-01A-11D-A22X-09 TCGA-A2-A3XT-10A-01D-A22X-09 g.chrX:53575991C>T c.9964G>A c.(9964-9966)Gtc>Atc p.V3322I BRCA 23 53577889 53577889 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:53577889C>T c.9358G>A c.(9358-9360)Gca>Aca p.A3120T BRCA 23 53579640 53579640 + Frame_Shift_Del DEL C C - TCGA-A8-A07J-01A-11W-A019-09 TCGA-A8-A07J-10A-01W-A021-09 g.chrX:53579640delC c.8709delG c.(8707-8709)aggfs p.R2903fs BRCA 23 53579644 53579645 + Frame_Shift_Del DEL CC CC - TCGA-A8-A07J-01A-11W-A019-09 TCGA-A8-A07J-10A-01W-A021-09 g.chrX:53579644_53579645delCC c.8704_8705delGG c.(8704-8706)ggcfs p.G2902fs BRCA 23 53579648 53579649 + Frame_Shift_Ins INS - - C TCGA-A8-A07J-01A-11W-A019-09 TCGA-A8-A07J-10A-01W-A021-09 g.chrX:53579648_53579649insC c.8700_8701insG c.(8698-8703)gtgcaafs p.Q2901fs BRCA 23 53581746 53581746 + Missense_Mutation SNP C C T TCGA-D8-A27F-01A-11D-A16D-09 TCGA-D8-A27F-10A-01D-A16D-09 g.chrX:53581746C>T c.8342G>A c.(8341-8343)gGa>gAa p.G2781E BRCA 23 53587267 53587267 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chrX:53587267T>G c.7618A>C c.(7618-7620)Acc>Ccc p.T2540P BRCA 23 53588774 53588774 + Missense_Mutation SNP G G A TCGA-BH-A1FM-01A-11D-A13L-09 TCGA-BH-A1FM-11B-23D-A188-09 g.chrX:53588774G>A c.7450C>T c.(7450-7452)Cgc>Tgc p.R2484C BRCA 23 53589093 53589093 + Silent SNP C C T TCGA-EW-A1IZ-01A-11D-A188-09 TCGA-EW-A1IZ-10A-01D-A13O-09 g.chrX:53589093C>T c.7317G>A c.(7315-7317)gaG>gaA p.E2439E BRCA 23 53589161 53589161 + Missense_Mutation SNP G G C TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chrX:53589161G>C c.7249C>G c.(7249-7251)Cag>Gag p.Q2417E BRCA 23 53589797 53589797 + Missense_Mutation SNP C C T TCGA-BH-A0B0-01A-21D-A10Y-09 TCGA-BH-A0B0-10A-01D-A110-09 g.chrX:53589797C>T c.7199G>A c.(7198-7200)cGa>cAa p.R2400Q BRCA 23 53589824 53589824 + Missense_Mutation SNP C C G TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chrX:53589824C>G c.7172G>C c.(7171-7173)aGc>aCc p.S2391T BRCA 23 53596651 53596651 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chrX:53596651A>C c.6449T>G c.(6448-6450)gTg>gGg p.V2150G BRCA 23 53602625 53602625 + Missense_Mutation SNP G G A TCGA-A7-A3J1-01A-11D-A20S-09 TCGA-A7-A3J1-10A-01D-A20S-09 g.chrX:53602625G>A c.6008C>T c.(6007-6009)aCg>aTg p.T2003M BRCA 23 53610641 53610641 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:53610641C>G c.5397G>C c.(5395-5397)aaG>aaC p.K1799N BRCA 23 53610743 53610743 + Missense_Mutation SNP C C A TCGA-LL-A5YP-01A-21D-A28B-09 TCGA-LL-A5YP-10A-01D-A28E-09 g.chrX:53610743C>A c.5295G>T c.(5293-5295)atG>atT p.M1765I BRCA 23 53616683 53616683 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chrX:53616683C>T c.4285G>A c.(4285-4287)Gac>Aac p.D1429N BRCA 23 53617397 53617397 + Missense_Mutation SNP A A T TCGA-BH-A0BZ-01A-31D-A12Q-09 TCGA-BH-A0BZ-11A-61D-A12Q-09 g.chrX:53617397A>T c.4158T>A c.(4156-4158)gaT>gaA p.D1386E BRCA 23 53631552 53631552 + Missense_Mutation SNP G G C TCGA-LL-A5YN-01A-11D-A28B-09 TCGA-LL-A5YN-10A-01D-A28E-09 g.chrX:53631552G>C c.2740C>G c.(2740-2742)Cag>Gag p.Q914E BRCA 23 53631744 53631744 + Missense_Mutation SNP A A C TCGA-C8-A27B-01A-11D-A167-09 TCGA-C8-A27B-10A-01D-A167-09 g.chrX:53631744A>C c.2548T>G c.(2548-2550)Tcc>Gcc p.S850A BRCA 23 53642741 53642741 + Silent SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:53642741G>A c.2013C>T c.(2011-2013)ccC>ccT p.P671P BRCA 23 53644041 53644041 + Missense_Mutation SNP C C A TCGA-BH-A18P-01A-11D-A12B-09 TCGA-BH-A18P-11A-43D-A12B-09 g.chrX:53644041C>A c.1847G>T c.(1846-1848)cGa>cTa p.R616L BRCA 23 53644083 53644083 + Missense_Mutation SNP C C G TCGA-A8-A09A-01A-11W-A019-09 TCGA-A8-A09A-10A-01W-A062-09 g.chrX:53644083C>G c.1805G>C c.(1804-1806)gGc>gCc p.G602A BRCA 23 53652126 53652126 + Missense_Mutation SNP A A G TCGA-A2-A1FW-01A-11D-A13L-09 TCGA-A2-A1FW-10A-01D-A13O-09 g.chrX:53652126A>G c.1583T>C c.(1582-1584)aTa>aCa p.I528T BRCA 23 53655570 53655570 + Splice_Site SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chrX:53655570A>G c.1116T>C c.(1114-1116)gaT>gaC p.D372D BRCA 23 53661226 53661226 + Missense_Mutation SNP A A T TCGA-AN-A0XW-01A-11D-A10G-09 TCGA-AN-A0XW-10A-01D-A10G-09 g.chrX:53661226A>T c.529T>A c.(529-531)Ttt>Att p.F177I BRCA 23 53675211 53675211 + Missense_Mutation SNP T T C TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chrX:53675211T>C c.88A>G c.(88-90)Aat>Gat p.N30D CESC 23 53560326 53560326 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:53560326G>A c.13069C>T c.(13069-13071)Cgc>Tgc p.R4357C CESC 23 53564520 53564520 + Missense_Mutation SNP C C T TCGA-C5-A7CO-01A-11D-A351-09 TCGA-C5-A7CO-10A-01D-A351-09 g.chrX:53564520C>T c.12134G>A c.(12133-12135)cGa>cAa p.R4045Q CESC 23 53564617 53564617 + Missense_Mutation SNP G G A TCGA-FU-A3TX-01A-11D-A22X-09 TCGA-FU-A3TX-10A-01D-A22X-09 g.chrX:53564617G>A c.12037C>T c.(12037-12039)Cgg>Tgg p.R4013W CESC 23 53579331 53579331 + Missense_Mutation SNP C C T TCGA-C5-A1MK-01A-11D-A14W-08 TCGA-C5-A1MK-10A-01D-A14W-08 g.chrX:53579331C>T c.8822G>A c.(8821-8823)cGa>cAa p.R2941Q CESC 23 53579708 53579708 + Missense_Mutation SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chrX:53579708C>T c.8641G>A c.(8641-8643)Gag>Aag p.E2881K CESC 23 53579732 53579732 + Missense_Mutation SNP C C T TCGA-IR-A3LI-01A-11D-A20U-09 TCGA-IR-A3LI-10A-01D-A20U-09 g.chrX:53579732C>T c.8617G>A c.(8617-8619)Gac>Aac p.D2873N CESC 23 53588727 53588727 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:53588727G>C c.7497C>G c.(7495-7497)ttC>ttG p.F2499L CESC 23 53589104 53589104 + Missense_Mutation SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:53589104C>T c.7306G>A c.(7306-7308)Gag>Aag p.E2436K CESC 23 53589158 53589158 + Nonsense_Mutation SNP C C A TCGA-EK-A3GJ-01A-21D-A20U-09 TCGA-EK-A3GJ-11A-11D-A20U-09 g.chrX:53589158C>A c.7252G>T c.(7252-7254)Gaa>Taa p.E2418* CESC 23 53589843 53589843 + Missense_Mutation SNP C C T TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chrX:53589843C>T c.7153G>A c.(7153-7155)Gaa>Aaa p.E2385K CESC 23 53591561 53591561 + Missense_Mutation SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chrX:53591561C>G c.7003G>C c.(7003-7005)Gag>Cag p.E2335Q CESC 23 53615416 53615416 + Missense_Mutation SNP T T C TCGA-HM-A3JK-01A-11D-A21Q-09 TCGA-HM-A3JK-10A-01D-A21Q-09 g.chrX:53615416T>C c.4540A>G c.(4540-4542)Ata>Gta p.I1514V CESC 23 53643957 53643957 + Missense_Mutation SNP C C T TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chrX:53643957C>T c.1931G>A c.(1930-1932)cGg>cAg p.R644Q CESC 23 53644394 53644394 + Silent SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chrX:53644394C>T c.1686G>A c.(1684-1686)gtG>gtA p.V562V CESC 23 53655822 53655822 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:53655822G>C c.995C>G c.(994-996)aCa>aGa p.T332R CESC 23 53672359 53672359 + Missense_Mutation SNP A A C TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chrX:53672359A>C c.408T>G c.(406-408)aaT>aaG p.N136K CESC 23 53675225 53675225 + Missense_Mutation SNP T T G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chrX:53675225T>G c.74A>C c.(73-75)aAa>aCa p.K25T CHOL 23 53570921 53570921 + Missense_Mutation SNP C C A TCGA-W5-AA38-01A-11D-A417-09 TCGA-W5-AA38-10A-01D-A41A-09 g.chrX:53570921C>A c.11260G>T c.(11260-11262)Ggt>Tgt p.G3754C COAD 23 53562355 53562355 + Missense_Mutation SNP C C G TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chrX:53562355C>G c.12639G>C c.(12637-12639)atG>atC p.M4213I COAD 23 53562375 53562375 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:53562375C>T c.12619G>A c.(12619-12621)Gta>Ata p.V4207I COAD 23 53563202 53563202 + Missense_Mutation SNP A A G TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chrX:53563202A>G c.12437T>C c.(12436-12438)aTg>aCg p.M4146T COAD 23 53563519 53563519 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:53563519T>C c.12247A>G c.(12247-12249)Acc>Gcc p.T4083A COAD 23 53563520 53563520 + Silent SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chrX:53563520A>G c.12246T>C c.(12244-12246)cgT>cgC p.R4082R COAD 23 53563522 53563522 + Missense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chrX:53563522G>A c.12244C>T c.(12244-12246)Cgt>Tgt p.R4082C COAD 23 53563522 53563522 + Missense_Mutation SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chrX:53563522G>A c.12244C>T c.(12244-12246)Cgt>Tgt p.R4082C COAD 23 53563522 53563522 + Missense_Mutation SNP G G T TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chrX:53563522G>T c.12244C>A c.(12244-12246)Cgt>Agt p.R4082S COAD 23 53564590 53564590 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:53564590G>A c.12064C>T c.(12064-12066)Cgt>Tgt p.R4022C COAD 23 53564590 53564590 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:53564590G>A c.12064C>T c.(12064-12066)Cgt>Tgt p.R4022C COAD 23 53565307 53565307 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53565307A>G c.11987T>C c.(11986-11988)gTc>gCc p.V3996A COAD 23 53565948 53565948 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chrX:53565948G>A c.11726C>T c.(11725-11727)gCa>gTa p.A3909V COAD 23 53565984 53565984 + Missense_Mutation SNP T T C TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chrX:53565984T>C c.11690A>G c.(11689-11691)aAg>aGg p.K3897R COAD 23 53566740 53566740 + Missense_Mutation SNP T T A TCGA-AA-3854-01A-01W-0900-09 TCGA-AA-3854-10A-01W-0900-09 g.chrX:53566740T>A c.11510A>T c.(11509-11511)aAg>aTg p.K3837M COAD 23 53570859 53570859 + Silent SNP G G A TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chrX:53570859G>A c.11322C>T c.(11320-11322)gcC>gcT p.A3774A COAD 23 53571521 53571521 + Splice_Site SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chrX:53571521C>A c.11251G>T c.(11251-11253)Ggt>Tgt p.G3751C COAD 23 53571567 53571567 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:53571567G>A c.11205C>T c.(11203-11205)gaC>gaT p.D3735D COAD 23 53571600 53571600 + Missense_Mutation SNP C C G TCGA-AA-A02F-01A-01W-A00E-09 TCGA-AA-A02F-10A-01W-A00E-09 g.chrX:53571600C>G c.11172G>C c.(11170-11172)ttG>ttC p.L3724F COAD 23 53571652 53571652 + Missense_Mutation SNP A A G TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:53571652A>G c.11120T>C c.(11119-11121)cTg>cCg p.L3707P COAD 23 53573424 53573424 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53573424G>A c.10888C>T c.(10888-10890)Ctg>Ttg p.L3630L COAD 23 53573497 53573497 + Silent SNP T T C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53573497T>C c.10815A>G c.(10813-10815)ctA>ctG p.L3605L COAD 23 53574943 53574943 + Missense_Mutation SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:53574943T>C c.10327A>G c.(10327-10329)Atc>Gtc p.I3443V COAD 23 53576154 53576154 + Silent SNP A A G TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chrX:53576154A>G c.9801T>C c.(9799-9801)cgT>cgC p.R3267R COAD 23 53576156 53576156 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:53576156G>A c.9799C>T c.(9799-9801)Cgt>Tgt p.R3267C COAD 23 53576434 53576434 + Missense_Mutation SNP C C T TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chrX:53576434C>T c.9521G>A c.(9520-9522)cGc>cAc p.R3174H COAD 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q COAD 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q COAD 23 53577972 53577972 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:53577972T>C c.9275A>G c.(9274-9276)gAg>gGg p.E3092G COAD 23 53579614 53579614 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chrX:53579614T>C c.8735A>G c.(8734-8736)cAg>cGg p.Q2912R COAD 23 53581673 53581673 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53581673C>T c.8415G>A c.(8413-8415)gaG>gaA p.E2805E COAD 23 53581681 53581681 + Missense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chrX:53581681G>A c.8407C>T c.(8407-8409)Cct>Tct p.P2803S COAD 23 53587174 53587174 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chrX:53587174G>A c.7711C>T c.(7711-7713)Ccc>Tcc p.P2571S COAD 23 53587256 53587256 + Silent SNP G G A TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chrX:53587256G>A c.7629C>T c.(7627-7629)atC>atT p.I2543I COAD 23 53589856 53589856 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chrX:53589856G>A c.7140C>T c.(7138-7140)gaC>gaT p.D2380D COAD 23 53591617 53591617 + Missense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:53591617C>A c.6947G>T c.(6946-6948)gGg>gTg p.G2316V COAD 23 53595719 53595719 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:53595719G>A c.6640C>T c.(6640-6642)Cgg>Tgg p.R2214W COAD 23 53596606 53596606 + Missense_Mutation SNP G G C TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chrX:53596606G>C c.6494C>G c.(6493-6495)gCt>gGt p.A2165G COAD 23 53602132 53602132 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:53602132C>A c.6080G>T c.(6079-6081)gGg>gTg p.G2027V COAD 23 53603879 53603879 + Silent SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chrX:53603879T>C c.5865A>G c.(5863-5865)gcA>gcG p.A1955A COAD 23 53610812 53610812 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:53610812G>A c.5226C>T c.(5224-5226)atC>atT p.I1742I COAD 23 53610837 53610837 + Missense_Mutation SNP T T C TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chrX:53610837T>C c.5201A>G c.(5200-5202)gAg>gGg p.E1734G COAD 23 53613484 53613484 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chrX:53613484G>A c.4790C>T c.(4789-4791)gCc>gTc p.A1597V COAD 23 53615446 53615446 + Missense_Mutation SNP T T G TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:53615446T>G c.4510A>C c.(4510-4512)Aca>Cca p.T1504P COAD 23 53616554 53616554 + Missense_Mutation SNP T T C TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chrX:53616554T>C c.4414A>G c.(4414-4416)Aat>Gat p.N1472D COAD 23 53616678 53616678 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53616678C>T c.4290G>A c.(4288-4290)ccG>ccA p.P1430P COAD 23 53616745 53616745 + Missense_Mutation SNP C C A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chrX:53616745C>A c.4223G>T c.(4222-4224)cGg>cTg p.R1408L COAD 23 53620419 53620419 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:53620419G>T c.3646C>A c.(3646-3648)Ctt>Att p.L1216I COAD 23 53622234 53622234 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:53622234G>A c.3293C>T c.(3292-3294)gCg>gTg p.A1098V COAD 23 53631607 53631607 + Silent SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chrX:53631607T>C c.2685A>G c.(2683-2685)gcA>gcG p.A895A COAD 23 53644317 53644317 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53644317G>A c.1763C>T c.(1762-1764)gCa>gTa p.A588V COAD 23 53654407 53654407 + Silent SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chrX:53654407T>C c.1443A>G c.(1441-1443)agA>agG p.R481R COAD 23 53654407 53654407 + Silent SNP T T C TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chrX:53654407T>C c.1443A>G c.(1441-1443)agA>agG p.R481R COAD 23 53654409 53654409 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chrX:53654409T>C c.1441A>G c.(1441-1443)Aga>Gga p.R481G COAD 23 53654409 53654409 + Missense_Mutation SNP T T C TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chrX:53654409T>C c.1441A>G c.(1441-1443)Aga>Gga p.R481G COAD 23 53654789 53654789 + Missense_Mutation SNP A A C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:53654789A>C c.1284T>G c.(1282-1284)ttT>ttG p.F428L COAD 23 53654811 53654811 + Missense_Mutation SNP T T C TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chrX:53654811T>C c.1262A>G c.(1261-1263)gAt>gGt p.D421G COAD 23 53655545 53655545 + Nonsense_Mutation SNP G G A TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chrX:53655545G>A c.1141C>T c.(1141-1143)Cag>Tag p.Q381* COAD 23 53655545 53655545 + Nonsense_Mutation SNP G G A TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chrX:53655545G>A c.1141C>T c.(1141-1143)Cag>Tag p.Q381* COAD 23 53658403 53658403 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:53658403G>A c.725C>T c.(724-726)tCt>tTt p.S242F COAD 23 53672374 53672374 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:53672374C>T c.393G>A c.(391-393)gtG>gtA p.V131V COAD 23 53674479 53674479 + Silent SNP G G A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chrX:53674479G>A c.183C>T c.(181-183)ttC>ttT p.F61F COADREAD 23 53561010 53561010 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:53561010C>T c.12980G>A c.(12979-12981)cGa>cAa p.R4327Q COADREAD 23 53562355 53562355 + Missense_Mutation SNP C C G TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chrX:53562355C>G c.12639G>C c.(12637-12639)atG>atC p.M4213I COADREAD 23 53562375 53562375 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:53562375C>T c.12619G>A c.(12619-12621)Gta>Ata p.V4207I COADREAD 23 53563202 53563202 + Missense_Mutation SNP A A G TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chrX:53563202A>G c.12437T>C c.(12436-12438)aTg>aCg p.M4146T COADREAD 23 53563519 53563519 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:53563519T>C c.12247A>G c.(12247-12249)Acc>Gcc p.T4083A COADREAD 23 53563520 53563520 + Silent SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chrX:53563520A>G c.12246T>C c.(12244-12246)cgT>cgC p.R4082R COADREAD 23 53563522 53563522 + Missense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chrX:53563522G>A c.12244C>T c.(12244-12246)Cgt>Tgt p.R4082C COADREAD 23 53563522 53563522 + Missense_Mutation SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chrX:53563522G>A c.12244C>T c.(12244-12246)Cgt>Tgt p.R4082C COADREAD 23 53563522 53563522 + Missense_Mutation SNP G G T TCGA-CM-6167-01A-11D-1650-10 TCGA-CM-6167-10A-01D-1650-10 g.chrX:53563522G>T c.12244C>A c.(12244-12246)Cgt>Agt p.R4082S COADREAD 23 53564590 53564590 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:53564590G>A c.12064C>T c.(12064-12066)Cgt>Tgt p.R4022C COADREAD 23 53564590 53564590 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:53564590G>A c.12064C>T c.(12064-12066)Cgt>Tgt p.R4022C COADREAD 23 53565307 53565307 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53565307A>G c.11987T>C c.(11986-11988)gTc>gCc p.V3996A COADREAD 23 53565406 53565406 + Missense_Mutation SNP C C T TCGA-AG-A020-01A-21W-A096-10 TCGA-AG-A020-11A-11W-A096-10 g.chrX:53565406C>T c.11888G>A c.(11887-11889)cGc>cAc p.R3963H COADREAD 23 53565948 53565948 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chrX:53565948G>A c.11726C>T c.(11725-11727)gCa>gTa p.A3909V COADREAD 23 53565984 53565984 + Missense_Mutation SNP T T C TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chrX:53565984T>C c.11690A>G c.(11689-11691)aAg>aGg p.K3897R COADREAD 23 53566740 53566740 + Missense_Mutation SNP T T A TCGA-AA-3854-01A-01W-0900-09 TCGA-AA-3854-10A-01W-0900-09 g.chrX:53566740T>A c.11510A>T c.(11509-11511)aAg>aTg p.K3837M COADREAD 23 53570859 53570859 + Silent SNP G G A TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chrX:53570859G>A c.11322C>T c.(11320-11322)gcC>gcT p.A3774A COADREAD 23 53571521 53571521 + Splice_Site SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chrX:53571521C>A c.11251G>T c.(11251-11253)Ggt>Tgt p.G3751C COADREAD 23 53571567 53571567 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:53571567G>A c.11205C>T c.(11203-11205)gaC>gaT p.D3735D COADREAD 23 53571600 53571600 + Missense_Mutation SNP C C G TCGA-AA-A02F-01A-01W-A00E-09 TCGA-AA-A02F-10A-01W-A00E-09 g.chrX:53571600C>G c.11172G>C c.(11170-11172)ttG>ttC p.L3724F COADREAD 23 53571652 53571652 + Missense_Mutation SNP A A G TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chrX:53571652A>G c.11120T>C c.(11119-11121)cTg>cCg p.L3707P COADREAD 23 53573424 53573424 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53573424G>A c.10888C>T c.(10888-10890)Ctg>Ttg p.L3630L COADREAD 23 53573497 53573497 + Silent SNP T T C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53573497T>C c.10815A>G c.(10813-10815)ctA>ctG p.L3605L COADREAD 23 53574917 53574917 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:53574917C>A c.10353G>T c.(10351-10353)gaG>gaT p.E3451D COADREAD 23 53574943 53574943 + Missense_Mutation SNP T T C TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:53574943T>C c.10327A>G c.(10327-10329)Atc>Gtc p.I3443V COADREAD 23 53576154 53576154 + Silent SNP A A G TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chrX:53576154A>G c.9801T>C c.(9799-9801)cgT>cgC p.R3267R COADREAD 23 53576156 53576156 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:53576156G>A c.9799C>T c.(9799-9801)Cgt>Tgt p.R3267C COADREAD 23 53576434 53576434 + Missense_Mutation SNP C C T TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chrX:53576434C>T c.9521G>A c.(9520-9522)cGc>cAc p.R3174H COADREAD 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q COADREAD 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q COADREAD 23 53577972 53577972 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:53577972T>C c.9275A>G c.(9274-9276)gAg>gGg p.E3092G COADREAD 23 53579614 53579614 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chrX:53579614T>C c.8735A>G c.(8734-8736)cAg>cGg p.Q2912R COADREAD 23 53581673 53581673 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53581673C>T c.8415G>A c.(8413-8415)gaG>gaA p.E2805E COADREAD 23 53581681 53581681 + Missense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chrX:53581681G>A c.8407C>T c.(8407-8409)Cct>Tct p.P2803S COADREAD 23 53587174 53587174 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chrX:53587174G>A c.7711C>T c.(7711-7713)Ccc>Tcc p.P2571S COADREAD 23 53587256 53587256 + Silent SNP G G A TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chrX:53587256G>A c.7629C>T c.(7627-7629)atC>atT p.I2543I COADREAD 23 53589856 53589856 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chrX:53589856G>A c.7140C>T c.(7138-7140)gaC>gaT p.D2380D COADREAD 23 53591617 53591617 + Missense_Mutation SNP C C A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:53591617C>A c.6947G>T c.(6946-6948)gGg>gTg p.G2316V COADREAD 23 53595719 53595719 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:53595719G>A c.6640C>T c.(6640-6642)Cgg>Tgg p.R2214W COADREAD 23 53596606 53596606 + Missense_Mutation SNP G G C TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chrX:53596606G>C c.6494C>G c.(6493-6495)gCt>gGt p.A2165G COADREAD 23 53602132 53602132 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:53602132C>A c.6080G>T c.(6079-6081)gGg>gTg p.G2027V COADREAD 23 53603879 53603879 + Silent SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chrX:53603879T>C c.5865A>G c.(5863-5865)gcA>gcG p.A1955A COADREAD 23 53610679 53610679 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chrX:53610679G>A c.5359C>T c.(5359-5361)Cgg>Tgg p.R1787W COADREAD 23 53610812 53610812 + Silent SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:53610812G>A c.5226C>T c.(5224-5226)atC>atT p.I1742I COADREAD 23 53610837 53610837 + Missense_Mutation SNP T T C TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chrX:53610837T>C c.5201A>G c.(5200-5202)gAg>gGg p.E1734G COADREAD 23 53613484 53613484 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chrX:53613484G>A c.4790C>T c.(4789-4791)gCc>gTc p.A1597V COADREAD 23 53615446 53615446 + Missense_Mutation SNP T T G TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chrX:53615446T>G c.4510A>C c.(4510-4512)Aca>Cca p.T1504P COADREAD 23 53616547 53616547 + Missense_Mutation SNP G G C TCGA-DY-A1DF-01A-11D-A152-10 TCGA-DY-A1DF-10A-01D-A152-10 g.chrX:53616547G>C c.4421C>G c.(4420-4422)gCa>gGa p.A1474G COADREAD 23 53616554 53616554 + Missense_Mutation SNP T T C TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chrX:53616554T>C c.4414A>G c.(4414-4416)Aat>Gat p.N1472D COADREAD 23 53616678 53616678 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:53616678C>T c.4290G>A c.(4288-4290)ccG>ccA p.P1430P COADREAD 23 53616745 53616745 + Missense_Mutation SNP C C A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chrX:53616745C>A c.4223G>T c.(4222-4224)cGg>cTg p.R1408L COADREAD 23 53620419 53620419 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:53620419G>T c.3646C>A c.(3646-3648)Ctt>Att p.L1216I COADREAD 23 53622234 53622234 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:53622234G>A c.3293C>T c.(3292-3294)gCg>gTg p.A1098V COADREAD 23 53631607 53631607 + Silent SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chrX:53631607T>C c.2685A>G c.(2683-2685)gcA>gcG p.A895A COADREAD 23 53642763 53642763 + Missense_Mutation SNP T T A TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chrX:53642763T>A c.1991A>T c.(1990-1992)gAt>gTt p.D664V COADREAD 23 53644317 53644317 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:53644317G>A c.1763C>T c.(1762-1764)gCa>gTa p.A588V COADREAD 23 53654407 53654407 + Silent SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chrX:53654407T>C c.1443A>G c.(1441-1443)agA>agG p.R481R COADREAD 23 53654407 53654407 + Silent SNP T T C TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chrX:53654407T>C c.1443A>G c.(1441-1443)agA>agG p.R481R COADREAD 23 53654409 53654409 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chrX:53654409T>C c.1441A>G c.(1441-1443)Aga>Gga p.R481G COADREAD 23 53654409 53654409 + Missense_Mutation SNP T T C TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chrX:53654409T>C c.1441A>G c.(1441-1443)Aga>Gga p.R481G COADREAD 23 53654789 53654789 + Missense_Mutation SNP A A C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chrX:53654789A>C c.1284T>G c.(1282-1284)ttT>ttG p.F428L COADREAD 23 53654811 53654811 + Missense_Mutation SNP T T C TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chrX:53654811T>C c.1262A>G c.(1261-1263)gAt>gGt p.D421G COADREAD 23 53655545 53655545 + Nonsense_Mutation SNP G G A TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chrX:53655545G>A c.1141C>T c.(1141-1143)Cag>Tag p.Q381* COADREAD 23 53655545 53655545 + Nonsense_Mutation SNP G G A TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chrX:53655545G>A c.1141C>T c.(1141-1143)Cag>Tag p.Q381* COADREAD 23 53658403 53658403 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:53658403G>A c.725C>T c.(724-726)tCt>tTt p.S242F COADREAD 23 53672374 53672374 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:53672374C>T c.393G>A c.(391-393)gtG>gtA p.V131V COADREAD 23 53674479 53674479 + Silent SNP G G A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chrX:53674479G>A c.183C>T c.(181-183)ttC>ttT p.F61F DLBC 23 53654402 53654402 + Missense_Mutation SNP T T C TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chrX:53654402T>C c.1448A>G c.(1447-1449)aAt>aGt p.N483S ESCA 23 53561025 53561025 + Missense_Mutation SNP T T C TCGA-L5-A893-01A-11D-A36J-09 TCGA-L5-A893-11A-21D-A36M-09 g.chrX:53561025T>C c.12965A>G c.(12964-12966)aAg>aGg p.K4322R ESCA 23 53562355 53562355 + Missense_Mutation SNP C C T TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chrX:53562355C>T c.12639G>A c.(12637-12639)atG>atA p.M4213I ESCA 23 53565335 53565335 + Missense_Mutation SNP C C T TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chrX:53565335C>T c.11959G>A c.(11959-11961)Gac>Aac p.D3987N ESCA 23 53570860 53570860 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chrX:53570860G>A c.11321C>T c.(11320-11322)gCc>gTc p.A3774V ESCA 23 53573489 53573489 + Missense_Mutation SNP A A C TCGA-LN-A4A5-01A-21D-A27G-09 TCGA-LN-A4A5-10A-01D-A27G-09 g.chrX:53573489A>C c.10823T>G c.(10822-10824)cTc>cGc p.L3608R ESCA 23 53575129 53575129 + Missense_Mutation SNP T T C TCGA-Q9-A6FU-01A-11D-A31U-09 TCGA-Q9-A6FU-10A-01D-A31U-09 g.chrX:53575129T>C c.10141A>G c.(10141-10143)Agc>Ggc p.S3381G ESCA 23 53575167 53575167 + Missense_Mutation SNP C C T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chrX:53575167C>T c.10103G>A c.(10102-10104)gGc>gAc p.G3368D ESCA 23 53576031 53576031 + Frame_Shift_Del DEL C C - TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chrX:53576031delC c.9924delG c.(9922-9924)gggfs p.G3308fs ESCA 23 53576405 53576405 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chrX:53576405C>T c.9550G>A c.(9550-9552)Gaa>Aaa p.E3184K ESCA 23 53577971 53577971 + Missense_Mutation SNP C C A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chrX:53577971C>A c.9276G>T c.(9274-9276)gaG>gaT p.E3092D ESCA 23 53579695 53579695 + Missense_Mutation SNP G G T TCGA-LN-A49R-01A-11D-A247-09 TCGA-LN-A49R-10A-01D-A247-09 g.chrX:53579695G>T c.8654C>A c.(8653-8655)gCa>gAa p.A2885E ESCA 23 53587251 53587251 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chrX:53587251C>T c.7634G>A c.(7633-7635)cGc>cAc p.R2545H ESCA 23 53596600 53596600 + Missense_Mutation SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chrX:53596600G>T c.6500C>A c.(6499-6501)gCt>gAt p.A2167D ESCA 23 53600757 53600757 + Missense_Mutation SNP T T A TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chrX:53600757T>A c.6265A>T c.(6265-6267)Att>Ttt p.I2089F ESCA 23 53600796 53600796 + Missense_Mutation SNP C C T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chrX:53600796C>T c.6226G>A c.(6226-6228)Gca>Aca p.A2076T ESCA 23 53602122 53602122 + Missense_Mutation SNP T T A TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chrX:53602122T>A c.6090A>T c.(6088-6090)caA>caT p.Q2030H ESCA 23 53602169 53602169 + Missense_Mutation SNP C C T TCGA-L5-A8NT-01A-11D-A37C-09 TCGA-L5-A8NT-11A-11D-A37F-09 g.chrX:53602169C>T c.6043G>A c.(6043-6045)Gct>Act p.A2015T ESCA 23 53630391 53630391 + Missense_Mutation SNP G G T TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chrX:53630391G>T c.2814C>A c.(2812-2814)agC>agA p.S938R ESCA 23 53631641 53631641 + Missense_Mutation SNP G G T TCGA-VR-A8EW-01A-11D-A36J-09 TCGA-VR-A8EW-10A-01D-A36M-09 g.chrX:53631641G>T c.2651C>A c.(2650-2652)aCc>aAc p.T884N ESCA 23 53635828 53635828 + Missense_Mutation SNP A A T TCGA-L5-A4OG-01A-11D-A27G-09 TCGA-L5-A4OG-11A-12D-A27G-09 g.chrX:53635828A>T c.2304T>A c.(2302-2304)gaT>gaA p.D768E ESCA 23 53641613 53641613 + Missense_Mutation SNP G G T TCGA-IG-A3QL-01A-11D-A247-09 TCGA-IG-A3QL-10A-01D-A247-09 g.chrX:53641613G>T c.2143C>A c.(2143-2145)Ccc>Acc p.P715T ESCA 23 53658551 53658551 + Missense_Mutation SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chrX:53658551G>T c.661C>A c.(661-663)Cta>Ata p.L221I ESCA 23 53661227 53661227 + Silent SNP G G T TCGA-L5-A8NJ-01A-11D-A36J-09 TCGA-L5-A8NJ-11A-11D-A36M-09 g.chrX:53661227G>T c.528C>A c.(526-528)ggC>ggA p.G176G GBM 23 53569470 53569470 + Missense_Mutation SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chrX:53569470G>A c.11410C>T c.(11410-11412)Cgg>Tgg p.R3804W GBM 23 53571567 53571567 + Silent SNP G G A TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chrX:53571567G>A c.11205C>T c.(11203-11205)gaC>gaT p.D3735D GBM 23 53573431 53573431 + Silent SNP G G A TCGA-06-0876-01A-01W-0424-08 TCGA-06-0876-10A-01W-0424-08 g.chrX:53573431G>A c.10881C>T c.(10879-10881)gcC>gcT p.A3627A GBM 23 53576344 53576344 + Missense_Mutation SNP C C T TCGA-12-0616-01A-01D-1492-08 TCGA-12-0616-10A-01D-1492-08 g.chrX:53576344C>T c.9611G>A c.(9610-9612)cGt>cAt p.R3204H GBM 23 53590731 53590731 + Missense_Mutation SNP C C T TCGA-14-1823-01A-01W-0643-08 TCGA-14-1823-10A-01W-0644-08 g.chrX:53590731C>T c.7081G>A c.(7081-7083)Gga>Aga p.G2361R GBM 23 53591568 53591568 + Frame_Shift_Del DEL C C - TCGA-19-5959-01A-11D-1696-08 TCGA-19-5959-11A-01D-1696-08 g.chrX:53591568delC c.6996delG c.(6994-6996)gggfs p.G2332fs GBM 23 53600812 53600812 + Silent SNP A A G TCGA-06-1804-01A-01D-1696-08 TCGA-06-1804-10A-01D-1696-08 g.chrX:53600812A>G c.6210T>C c.(6208-6210)acT>acC p.T2070T GBM 23 53612010 53612010 + Nonsense_Mutation SNP G G A TCGA-16-1045-01B-01W-0611-08 TCGA-16-1045-10B-01W-0611-08 g.chrX:53612010G>A c.4963C>T c.(4963-4965)Cga>Tga p.R1655* GBMLGG 23 53561480 53561480 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53561480A>C c.12828T>G c.(12826-12828)atT>atG p.I4276M GBMLGG 23 53569470 53569470 + Missense_Mutation SNP G G A TCGA-28-5218-01A-01D-1486-08 TCGA-28-5218-10A-01D-1486-08 g.chrX:53569470G>A c.11410C>T c.(11410-11412)Cgg>Tgg p.R3804W GBMLGG 23 53571567 53571567 + Silent SNP G G A TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chrX:53571567G>A c.11205C>T c.(11203-11205)gaC>gaT p.D3735D GBMLGG 23 53573431 53573431 + Silent SNP G G A TCGA-06-0876-01A-01W-0424-08 TCGA-06-0876-10A-01W-0424-08 g.chrX:53573431G>A c.10881C>T c.(10879-10881)gcC>gcT p.A3627A GBMLGG 23 53576145 53576145 + Missense_Mutation SNP G G T TCGA-P5-A781-01A-11D-A32B-08 TCGA-P5-A781-10A-01D-A329-08 g.chrX:53576145G>T c.9810C>A c.(9808-9810)gaC>gaA p.D3270E GBMLGG 23 53576344 53576344 + Missense_Mutation SNP C C T TCGA-12-0616-01A-01D-1492-08 TCGA-12-0616-10A-01D-1492-08 g.chrX:53576344C>T c.9611G>A c.(9610-9612)cGt>cAt p.R3204H GBMLGG 23 53579402 53579402 + Splice_Site SNP G G C TCGA-P5-A731-01A-11D-A32B-08 TCGA-P5-A731-10A-01D-A329-08 g.chrX:53579402G>C c.8751C>G c.(8749-8751)agC>agG p.S2917R GBMLGG 23 53590731 53590731 + Missense_Mutation SNP C C T TCGA-14-1823-01A-01W-0643-08 TCGA-14-1823-10A-01W-0644-08 g.chrX:53590731C>T c.7081G>A c.(7081-7083)Gga>Aga p.G2361R GBMLGG 23 53591568 53591568 + Frame_Shift_Del DEL C C - TCGA-19-5959-01A-11D-1696-08 TCGA-19-5959-11A-01D-1696-08 g.chrX:53591568delC c.6996delG c.(6994-6996)gggfs p.G2332fs GBMLGG 23 53600812 53600812 + Silent SNP A A G TCGA-06-1804-01A-01D-1696-08 TCGA-06-1804-10A-01D-1696-08 g.chrX:53600812A>G c.6210T>C c.(6208-6210)acT>acC p.T2070T GBMLGG 23 53612010 53612010 + Nonsense_Mutation SNP G G A TCGA-16-1045-01B-01W-0611-08 TCGA-16-1045-10B-01W-0611-08 g.chrX:53612010G>A c.4963C>T c.(4963-4965)Cga>Tga p.R1655* GBMLGG 23 53612074 53612074 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53612074G>A c.4899C>T c.(4897-4899)agC>agT p.S1633S GBMLGG 23 53613509 53613509 + Silent SNP G G A TCGA-TQ-A7RN-01A-11D-A33T-08 TCGA-TQ-A7RN-10A-01D-A33W-08 g.chrX:53613509G>A c.4765C>T c.(4765-4767)Ctg>Ttg p.L1589L GBMLGG 23 53618082 53618082 + Splice_Site SNP G G C TCGA-EZ-7264-01A-11D-2024-08 TCGA-EZ-7264-10A-01D-2024-08 g.chrX:53618082G>C c.3973C>G c.(3973-3975)Ctc>Gtc p.L1325V GBMLGG 23 53641542 53641542 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53641542C>T c.2214G>A c.(2212-2214)atG>atA p.M738I GBMLGG 23 53644041 53644041 + Missense_Mutation SNP C C A TCGA-S9-A6WH-01A-12D-A33T-08 TCGA-S9-A6WH-10A-01D-A33W-08 g.chrX:53644041C>A c.1847G>T c.(1846-1848)cGa>cTa p.R616L GBMLGG 23 53654434 53654434 + Silent SNP C C T TCGA-DU-7012-01A-11D-2024-08 TCGA-DU-7012-10A-01D-2024-08 g.chrX:53654434C>T c.1416G>A c.(1414-1416)ccG>ccA p.P472P GBMLGG 23 53654813 53654813 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53654813G>A c.1260C>T c.(1258-1260)ggC>ggT p.G420G HNSC 23 53560286 53560286 + Missense_Mutation SNP C C T TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chrX:53560286C>T c.13109G>A c.(13108-13110)gGc>gAc p.G4370D HNSC 23 53560308 53560308 + Missense_Mutation SNP C C A TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chrX:53560308C>A c.13087G>T c.(13087-13089)Gct>Tct p.A4363S HNSC 23 53560365 53560365 + Missense_Mutation SNP G G C TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chrX:53560365G>C c.13030C>G c.(13030-13032)Cag>Gag p.Q4344E HNSC 23 53560975 53560975 + Missense_Mutation SNP G G A TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chrX:53560975G>A c.13015C>T c.(13015-13017)Cac>Tac p.H4339Y HNSC 23 53560984 53560984 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:53560984G>A c.13006C>T c.(13006-13008)Cct>Tct p.P4336S HNSC 23 53560990 53560990 + Missense_Mutation SNP G G A TCGA-CV-7406-01A-11D-2078-08 TCGA-CV-7406-10A-01D-2078-08 g.chrX:53560990G>A c.13000C>T c.(13000-13002)Cgc>Tgc p.R4334C HNSC 23 53561067 53561067 + Missense_Mutation SNP A A C TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chrX:53561067A>C c.12923T>G c.(12922-12924)cTg>cGg p.L4308R HNSC 23 53561522 53561522 + Silent SNP C C G TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chrX:53561522C>G c.12786G>C c.(12784-12786)ctG>ctC p.L4262L HNSC 23 53562351 53562351 + Missense_Mutation SNP T T C TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chrX:53562351T>C c.12643A>G c.(12643-12645)Atg>Gtg p.M4215V HNSC 23 53562382 53562384 + In_Frame_Del DEL CTT CTT - TCGA-CQ-5330-01A-01D-1683-08 TCGA-CQ-5330-10A-01D-1683-08 g.chrX:53562382_53562384delCTT c.12610_12612delAAG c.(12610-12612)aagdel p.K4204del HNSC 23 53562382 53562384 + In_Frame_Del DEL CTT CTT - TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chrX:53562382_53562384delCTT c.12610_12612delAAG c.(12610-12612)aagdel p.K4204del HNSC 23 53563110 53563110 + Missense_Mutation SNP C C T TCGA-CN-A642-01A-12D-A30E-08 TCGA-CN-A642-10A-01D-A30H-08 g.chrX:53563110C>T c.12529G>A c.(12529-12531)Gag>Aag p.E4177K HNSC 23 53563110 53563110 + Missense_Mutation SNP C C T TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chrX:53563110C>T c.12529G>A c.(12529-12531)Gag>Aag p.E4177K HNSC 23 53563190 53563190 + Missense_Mutation SNP T T A TCGA-QK-A652-01A-11D-A30E-08 TCGA-QK-A652-10A-01D-A30H-08 g.chrX:53563190T>A c.12449A>T c.(12448-12450)gAt>gTt p.D4150V HNSC 23 53563194 53563194 + Missense_Mutation SNP C C T TCGA-CQ-7068-01A-11D-2078-08 TCGA-CQ-7068-10A-01D-2078-08 g.chrX:53563194C>T c.12445G>A c.(12445-12447)Gaa>Aaa p.E4149K HNSC 23 53563554 53563554 + Missense_Mutation SNP C C T TCGA-DQ-7596-01A-11D-2229-08 TCGA-DQ-7596-10D-01D-2229-08 g.chrX:53563554C>T c.12212G>A c.(12211-12213)cGa>cAa p.R4071Q HNSC 23 53563587 53563589 + In_Frame_Del DEL CCA CCA - TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chrX:53563587_53563589delCCA c.12177_12179delTGG c.(12175-12180)ggtggg>ggg p.4059_4060GG>G HNSC 23 53570870 53570870 + Missense_Mutation SNP C C T TCGA-BA-5557-01A-01D-1512-08 TCGA-BA-5557-10A-01D-1512-08 g.chrX:53570870C>T c.11311G>A c.(11311-11313)Gag>Aag p.E3771K HNSC 23 53570870 53570870 + Missense_Mutation SNP C C T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chrX:53570870C>T c.11311G>A c.(11311-11313)Gag>Aag p.E3771K HNSC 23 53571556 53571556 + Missense_Mutation SNP C C T TCGA-HD-7832-01A-11D-2129-08 TCGA-HD-7832-10A-01D-2129-08 g.chrX:53571556C>T c.11216G>A c.(11215-11217)cGg>cAg p.R3739Q HNSC 23 53571657 53571657 + Silent SNP G G C TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chrX:53571657G>C c.11115C>G c.(11113-11115)ctC>ctG p.L3705L HNSC 23 53571698 53571698 + Missense_Mutation SNP T T G TCGA-D6-6824-01A-11D-1912-08 TCGA-D6-6824-10A-01D-1912-08 g.chrX:53571698T>G c.11074A>C c.(11074-11076)Att>Ctt p.I3692L HNSC 23 53572036 53572036 + Missense_Mutation SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chrX:53572036C>T c.11002G>A c.(11002-11004)Gag>Aag p.E3668K HNSC 23 53573400 53573400 + Missense_Mutation SNP T T C TCGA-CQ-5334-01A-01D-1683-08 TCGA-CQ-5334-10A-01D-1683-08 g.chrX:53573400T>C c.10912A>G c.(10912-10914)Ata>Gta p.I3638V HNSC 23 53573555 53573555 + Splice_Site SNP T T A TCGA-CV-5442-01A-01D-1512-08 TCGA-CV-5442-11A-01D-1512-08 g.chrX:53573555T>A c.e69-2 HNSC 23 53575991 53575991 + Missense_Mutation SNP C C T TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chrX:53575991C>T c.9964G>A c.(9964-9966)Gtc>Atc p.V3322I HNSC 23 53577938 53577938 + Silent SNP C C A TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chrX:53577938C>A c.9309G>T c.(9307-9309)cgG>cgT p.R3103R HNSC 23 53577973 53577973 + Missense_Mutation SNP C C T TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chrX:53577973C>T c.9274G>A c.(9274-9276)Gag>Aag p.E3092K HNSC 23 53581597 53581597 + Missense_Mutation SNP T T C TCGA-D6-A6EK-01A-11D-A31L-08 TCGA-D6-A6EK-10A-01D-A31J-08 g.chrX:53581597T>C c.8491A>G c.(8491-8493)Ata>Gta p.I2831V HNSC 23 53587364 53587365 + Frame_Shift_Ins INS - - G TCGA-CR-6471-01A-11D-1870-08 TCGA-CR-6471-10A-01D-1870-08 g.chrX:53587364_53587365insG c.7520_7521insC c.(7519-7521)ccafs p.P2507fs HNSC 23 53588762 53588762 + Missense_Mutation SNP C C G TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chrX:53588762C>G c.7462G>C c.(7462-7464)Gag>Cag p.E2488Q HNSC 23 53588762 53588762 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chrX:53588762C>T c.7462G>A c.(7462-7464)Gag>Aag p.E2488K HNSC 23 53589155 53589155 + Missense_Mutation SNP C C T TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chrX:53589155C>T c.7255G>A c.(7255-7257)Gag>Aag p.E2419K HNSC 23 53589797 53589797 + Missense_Mutation SNP C C T TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chrX:53589797C>T c.7199G>A c.(7198-7200)cGa>cAa p.R2400Q HNSC 23 53592084 53592087 + Frame_Shift_Del DEL GACT GACT - TCGA-QK-A6II-01A-11D-A31L-08 TCGA-QK-A6II-10A-01D-A31J-08 g.chrX:53592084_53592087delGACT c.6821_6824delAGTC c.(6820-6825)aagtctfs p.KS2274fs HNSC 23 53600715 53600715 + Nonsense_Mutation SNP T T A TCGA-F7-A61W-01A-11D-A28R-08 TCGA-F7-A61W-10A-01D-A28U-08 g.chrX:53600715T>A c.6307A>T c.(6307-6309)Aaa>Taa p.K2103* HNSC 23 53602642 53602642 + Missense_Mutation SNP C C G TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chrX:53602642C>G c.5991G>C c.(5989-5991)caG>caC p.Q1997H HNSC 23 53612084 53612084 + Missense_Mutation SNP T T C TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chrX:53612084T>C c.4889A>G c.(4888-4890)tAc>tGc p.Y1630C HNSC 23 53613475 53613475 + Nonsense_Mutation SNP G G C TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chrX:53613475G>C c.4799C>G c.(4798-4800)tCa>tGa p.S1600* HNSC 23 53617986 53617986 + Missense_Mutation SNP G G A TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chrX:53617986G>A c.4069C>T c.(4069-4071)Cct>Tct p.P1357S HNSC 23 53618007 53618007 + Missense_Mutation SNP C C T TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chrX:53618007C>T c.4048G>A c.(4048-4050)Gag>Aag p.E1350K HNSC 23 53619384 53619384 + Missense_Mutation SNP G G C TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chrX:53619384G>C c.3946C>G c.(3946-3948)Caa>Gaa p.Q1316E HNSC 23 53619397 53619397 + Silent SNP G G A TCGA-CV-5978-01A-11D-1683-08 TCGA-CV-5978-11A-01D-1683-08 g.chrX:53619397G>A c.3933C>T c.(3931-3933)tcC>tcT p.S1311S HNSC 23 53619411 53619411 + Missense_Mutation SNP C C G TCGA-CQ-A4CB-01A-11D-A25D-08 TCGA-CQ-A4CB-10A-01D-A25E-08 g.chrX:53619411C>G c.3919G>C c.(3919-3921)Gag>Cag p.E1307Q HNSC 23 53620323 53620323 + Splice_Site SNP C C A TCGA-CV-A6JZ-01A-11D-A31L-08 TCGA-CV-A6JZ-10A-01D-A31J-08 g.chrX:53620323C>A c.e31+1 HNSC 23 53620464 53620464 + Missense_Mutation SNP C C T TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chrX:53620464C>T c.3601G>A c.(3601-3603)Gcc>Acc p.A1201T HNSC 23 53622348 53622348 + Missense_Mutation SNP C C T TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chrX:53622348C>T c.3179G>A c.(3178-3180)gGc>gAc p.G1060D HNSC 23 53631658 53631658 + Silent SNP G G A TCGA-BA-6871-01A-11D-1870-08 TCGA-BA-6871-10A-01D-1870-08 g.chrX:53631658G>A c.2634C>T c.(2632-2634)ggC>ggT p.G878G HNSC 23 53634558 53634558 + Missense_Mutation SNP G G A TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chrX:53634558G>A c.2422C>T c.(2422-2424)Ctt>Ttt p.L808F HNSC 23 53641650 53641650 + Silent SNP T T C TCGA-UF-A7J9-01A-12D-A34J-08 TCGA-UF-A7J9-10A-01D-A34M-08 g.chrX:53641650T>C c.2106A>G c.(2104-2106)ccA>ccG p.P702P HNSC 23 53654387 53654387 + Missense_Mutation SNP C C T TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chrX:53654387C>T c.1463G>A c.(1462-1464)gGa>gAa p.G488E HNSC 23 53655770 53655771 + Frame_Shift_Del DEL AC AC - TCGA-CV-A465-01A-11D-A25Y-08 TCGA-CV-A465-10A-01D-A25Y-08 g.chrX:53655770_53655771delAC c.1046_1047delGT c.(1045-1047)tgtfs p.C349fs HNSC 23 53658553 53658553 + Missense_Mutation SNP G G C TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chrX:53658553G>C c.659C>G c.(658-660)aCa>aGa p.T220R HNSC 23 53672318 53672318 + Missense_Mutation SNP C C G TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chrX:53672318C>G c.449G>C c.(448-450)cGt>cCt p.R150P HNSC 23 53674496 53674496 + Missense_Mutation SNP C C T TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chrX:53674496C>T c.166G>A c.(166-168)Gac>Aac p.D56N KICH 23 53586462 53586462 + Missense_Mutation SNP G G T TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chrX:53586462G>T c.7768C>A c.(7768-7770)Ctt>Att p.L2590I KICH 23 53615355 53615355 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:53615355G>A c.4601C>T c.(4600-4602)aCg>aTg p.T1534M KIPAN 23 53563622 53563622 + Missense_Mutation SNP T T C TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chrX:53563622T>C c.12144A>G c.(12142-12144)atA>atG p.I4048M KIPAN 23 53564526 53564526 + Missense_Mutation SNP T T G TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chrX:53564526T>G c.12128A>C c.(12127-12129)aAg>aCg p.K4043T KIPAN 23 53565805 53565805 + Missense_Mutation SNP G G T TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chrX:53565805G>T c.11869C>A c.(11869-11871)Cgc>Agc p.R3957S KIPAN 23 53565885 53565885 + Missense_Mutation SNP G G A TCGA-SX-A71W-01A-12D-A34Z-10 TCGA-SX-A71W-10A-01D-A34Z-10 g.chrX:53565885G>A c.11789C>T c.(11788-11790)tCc>tTc p.S3930F KIPAN 23 53566667 53566667 + Silent SNP C C A TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chrX:53566667C>A c.11583G>T c.(11581-11583)ggG>ggT p.G3861G KIPAN 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-CZ-4862-01A-01D-1373-10 TCGA-CZ-4862-11A-01D-1373-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q KIPAN 23 53579648 53579648 + Missense_Mutation SNP G G T TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chrX:53579648G>T c.8701C>A c.(8701-8703)Caa>Aaa p.Q2901K KIPAN 23 53579772 53579772 + Silent SNP T T A TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chrX:53579772T>A c.8577A>T c.(8575-8577)acA>acT p.T2859T KIPAN 23 53584383 53584383 + Silent SNP A A G TCGA-GL-A59T-01A-21D-A28G-10 TCGA-GL-A59T-10A-01D-A28G-10 g.chrX:53584383A>G c.8166T>C c.(8164-8166)acT>acC p.T2722T KIPAN 23 53585980 53585980 + Missense_Mutation SNP C C T TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chrX:53585980C>T c.7957G>A c.(7957-7959)Gaa>Aaa p.E2653K KIPAN 23 53586385 53586385 + Silent SNP G G T TCGA-B8-4143-01A-01D-1806-10 TCGA-B8-4143-11A-01D-1251-10 g.chrX:53586385G>T c.7845C>A c.(7843-7845)atC>atA p.I2615I KIPAN 23 53586462 53586462 + Missense_Mutation SNP G G T TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chrX:53586462G>T c.7768C>A c.(7768-7770)Ctt>Att p.L2590I KIPAN 23 53589174 53589174 + Silent SNP C C T TCGA-B3-8121-01A-21D-2396-08 TCGA-B3-8121-10A-01D-2396-08 g.chrX:53589174C>T c.7236G>A c.(7234-7236)gaG>gaA p.E2412E KIPAN 23 53595734 53595734 + Missense_Mutation SNP T T C TCGA-CJ-4900-01A-01D-1462-08 TCGA-CJ-4900-11A-01D-1462-08 g.chrX:53595734T>C c.6625A>G c.(6625-6627)Atg>Gtg p.M2209V KIPAN 23 53612105 53612105 + Missense_Mutation SNP C C A TCGA-BP-4991-01A-01D-1462-08 TCGA-BP-4991-11A-01D-1462-08 g.chrX:53612105C>A c.4868G>T c.(4867-4869)cGc>cTc p.R1623L KIPAN 23 53615355 53615355 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:53615355G>A c.4601C>T c.(4600-4602)aCg>aTg p.T1534M KIPAN 23 53615356 53615356 + Missense_Mutation SNP T T A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chrX:53615356T>A c.4600A>T c.(4600-4602)Acg>Tcg p.T1534S KIPAN 23 53616526 53616526 + Missense_Mutation SNP A A T TCGA-F9-A8NY-01A-11D-A35Z-10 TCGA-F9-A8NY-10A-01D-A35Z-10 g.chrX:53616526A>T c.4442T>A c.(4441-4443)cTg>cAg p.L1481Q KIPAN 23 53619440 53619440 + Missense_Mutation SNP C C T TCGA-5P-A9K0-01A-11D-A42J-10 TCGA-5P-A9K0-10A-01D-A42M-10 g.chrX:53619440C>T c.3890G>A c.(3889-3891)gGg>gAg p.G1297E KIPAN 23 53622278 53622278 + Missense_Mutation SNP C C A TCGA-BP-4774-01A-01D-1366-10 TCGA-BP-4774-11A-01D-1367-10 g.chrX:53622278C>A c.3249G>T c.(3247-3249)agG>agT p.R1083S KIPAN 23 53627271 53627271 + Splice_Site SNP T T C TCGA-2Z-A9JJ-01A-11D-A42J-10 TCGA-2Z-A9JJ-10A-01D-A42M-10 g.chrX:53627271T>C c.e28-2 KIPAN 23 53641606 53641606 + Missense_Mutation SNP C C G TCGA-UZ-A9PM-01A-21D-A382-10 TCGA-UZ-A9PM-10A-01D-A385-10 g.chrX:53641606C>G c.2150G>C c.(2149-2151)aGg>aCg p.R717T KIPAN 23 53674403 53674403 + Missense_Mutation SNP C C G TCGA-B0-5085-01A-01D-1462-08 TCGA-B0-5085-11A-01D-1462-08 g.chrX:53674403C>G c.259G>C c.(259-261)Gag>Cag p.E87Q KIPAN 23 53675215 53675215 + Silent SNP A A C TCGA-CJ-4897-01A-03D-1429-08 TCGA-CJ-4897-11A-01D-1429-08 g.chrX:53675215A>C c.84T>G c.(82-84)gtT>gtG p.V28V KIRC 23 53563622 53563622 + Missense_Mutation SNP T T C TCGA-B0-5712-01A-11D-1669-08 TCGA-B0-5712-11A-01D-1669-08 g.chrX:53563622T>C c.12144A>G c.(12142-12144)atA>atG p.I4048M KIRC 23 53564526 53564526 + Missense_Mutation SNP T T G TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chrX:53564526T>G c.12128A>C c.(12127-12129)aAg>aCg p.K4043T KIRC 23 53577912 53577912 + Missense_Mutation SNP A A T TCGA-CZ-4862-01A-01D-1373-10 TCGA-CZ-4862-11A-01D-1373-10 g.chrX:53577912A>T c.9335T>A c.(9334-9336)cTg>cAg p.L3112Q KIRC 23 53579648 53579648 + Missense_Mutation SNP G G T TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chrX:53579648G>T c.8701C>A c.(8701-8703)Caa>Aaa p.Q2901K KIRC 23 53579772 53579772 + Silent SNP T T A TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chrX:53579772T>A c.8577A>T c.(8575-8577)acA>acT p.T2859T KIRC 23 53585980 53585980 + Missense_Mutation SNP C C T TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chrX:53585980C>T c.7957G>A c.(7957-7959)Gaa>Aaa p.E2653K KIRC 23 53586385 53586385 + Silent SNP G G T TCGA-B8-4143-01A-01D-1806-10 TCGA-B8-4143-11A-01D-1251-10 g.chrX:53586385G>T c.7845C>A c.(7843-7845)atC>atA p.I2615I KIRC 23 53595734 53595734 + Missense_Mutation SNP T T C TCGA-CJ-4900-01A-01D-1462-08 TCGA-CJ-4900-11A-01D-1462-08 g.chrX:53595734T>C c.6625A>G c.(6625-6627)Atg>Gtg p.M2209V KIRC 23 53612105 53612105 + Missense_Mutation SNP C C A TCGA-BP-4991-01A-01D-1462-08 TCGA-BP-4991-11A-01D-1462-08 g.chrX:53612105C>A c.4868G>T c.(4867-4869)cGc>cTc p.R1623L KIRC 23 53615356 53615356 + Missense_Mutation SNP T T A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chrX:53615356T>A c.4600A>T c.(4600-4602)Acg>Tcg p.T1534S KIRC 23 53622278 53622278 + Missense_Mutation SNP C C A TCGA-BP-4774-01A-01D-1366-10 TCGA-BP-4774-11A-01D-1367-10 g.chrX:53622278C>A c.3249G>T c.(3247-3249)agG>agT p.R1083S KIRC 23 53674403 53674403 + Missense_Mutation SNP C C G TCGA-B0-5085-01A-01D-1462-08 TCGA-B0-5085-11A-01D-1462-08 g.chrX:53674403C>G c.259G>C c.(259-261)Gag>Cag p.E87Q KIRC 23 53675215 53675215 + Silent SNP A A C TCGA-CJ-4897-01A-03D-1429-08 TCGA-CJ-4897-11A-01D-1429-08 g.chrX:53675215A>C c.84T>G c.(82-84)gtT>gtG p.V28V KIRP 23 53565805 53565805 + Missense_Mutation SNP G G T TCGA-2Z-A9J5-01A-21D-A382-10 TCGA-2Z-A9J5-10A-01D-A385-10 g.chrX:53565805G>T c.11869C>A c.(11869-11871)Cgc>Agc p.R3957S KIRP 23 53565885 53565885 + Missense_Mutation SNP G G A TCGA-SX-A71W-01A-12D-A34Z-10 TCGA-SX-A71W-10A-01D-A34Z-10 g.chrX:53565885G>A c.11789C>T c.(11788-11790)tCc>tTc p.S3930F KIRP 23 53566667 53566667 + Silent SNP C C A TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chrX:53566667C>A c.11583G>T c.(11581-11583)ggG>ggT p.G3861G KIRP 23 53584383 53584383 + Silent SNP A A G TCGA-GL-A59T-01A-21D-A28G-10 TCGA-GL-A59T-10A-01D-A28G-10 g.chrX:53584383A>G c.8166T>C c.(8164-8166)acT>acC p.T2722T KIRP 23 53589174 53589174 + Silent SNP C C T TCGA-B3-8121-01A-21D-2396-08 TCGA-B3-8121-10A-01D-2396-08 g.chrX:53589174C>T c.7236G>A c.(7234-7236)gaG>gaA p.E2412E KIRP 23 53616526 53616526 + Missense_Mutation SNP A A T TCGA-F9-A8NY-01A-11D-A35Z-10 TCGA-F9-A8NY-10A-01D-A35Z-10 g.chrX:53616526A>T c.4442T>A c.(4441-4443)cTg>cAg p.L1481Q KIRP 23 53619440 53619440 + Missense_Mutation SNP C C T TCGA-5P-A9K0-01A-11D-A42J-10 TCGA-5P-A9K0-10A-01D-A42M-10 g.chrX:53619440C>T c.3890G>A c.(3889-3891)gGg>gAg p.G1297E KIRP 23 53627271 53627271 + Splice_Site SNP T T C TCGA-2Z-A9JJ-01A-11D-A42J-10 TCGA-2Z-A9JJ-10A-01D-A42M-10 g.chrX:53627271T>C c.e28-2 KIRP 23 53641606 53641606 + Missense_Mutation SNP C C G TCGA-UZ-A9PM-01A-21D-A382-10 TCGA-UZ-A9PM-10A-01D-A385-10 g.chrX:53641606C>G c.2150G>C c.(2149-2151)aGg>aCg p.R717T LGG 23 53561480 53561480 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53561480A>C c.12828T>G c.(12826-12828)atT>atG p.I4276M LGG 23 53576145 53576145 + Missense_Mutation SNP G G T TCGA-P5-A781-01A-11D-A32B-08 TCGA-P5-A781-10A-01D-A329-08 g.chrX:53576145G>T c.9810C>A c.(9808-9810)gaC>gaA p.D3270E LGG 23 53579402 53579402 + Splice_Site SNP G G C TCGA-P5-A731-01A-11D-A32B-08 TCGA-P5-A731-10A-01D-A329-08 g.chrX:53579402G>C c.8751C>G c.(8749-8751)agC>agG p.S2917R LGG 23 53612074 53612074 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53612074G>A c.4899C>T c.(4897-4899)agC>agT p.S1633S LGG 23 53613509 53613509 + Silent SNP G G A TCGA-TQ-A7RN-01A-11D-A33T-08 TCGA-TQ-A7RN-10A-01D-A33W-08 g.chrX:53613509G>A c.4765C>T c.(4765-4767)Ctg>Ttg p.L1589L LGG 23 53618082 53618082 + Splice_Site SNP G G C TCGA-EZ-7264-01A-11D-2024-08 TCGA-EZ-7264-10A-01D-2024-08 g.chrX:53618082G>C c.3973C>G c.(3973-3975)Ctc>Gtc p.L1325V LGG 23 53641542 53641542 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53641542C>T c.2214G>A c.(2212-2214)atG>atA p.M738I LGG 23 53644041 53644041 + Missense_Mutation SNP C C A TCGA-S9-A6WH-01A-12D-A33T-08 TCGA-S9-A6WH-10A-01D-A33W-08 g.chrX:53644041C>A c.1847G>T c.(1846-1848)cGa>cTa p.R616L LGG 23 53654434 53654434 + Silent SNP C C T TCGA-DU-7012-01A-11D-2024-08 TCGA-DU-7012-10A-01D-2024-08 g.chrX:53654434C>T c.1416G>A c.(1414-1416)ccG>ccA p.P472P LGG 23 53654813 53654813 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:53654813G>A c.1260C>T c.(1258-1260)ggC>ggT p.G420G LIHC 23 53561499 53561499 + Missense_Mutation SNP T T A TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chrX:53561499T>A c.12809A>T c.(12808-12810)aAg>aTg p.K4270M LIHC 23 53563161 53563161 + Missense_Mutation SNP G G C TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chrX:53563161G>C c.12478C>G c.(12478-12480)Ctg>Gtg p.L4160V LIHC 23 53565344 53565344 + Missense_Mutation SNP C C T TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chrX:53565344C>T c.11950G>A c.(11950-11952)Gtc>Atc p.V3984I LIHC 23 53574709 53574709 + Missense_Mutation SNP T T C TCGA-ZP-A9CY-01A-11D-A382-10 TCGA-ZP-A9CY-10B-01D-A385-10 g.chrX:53574709T>C c.10561A>G c.(10561-10563)Acg>Gcg p.T3521A LIHC 23 53579402 53579402 + Splice_Site SNP G G T TCGA-XR-A8TD-01A-12D-A38X-10 TCGA-XR-A8TD-10A-01D-A38X-10 g.chrX:53579402G>T c.8751C>A c.(8749-8751)agC>agA p.S2917R LIHC 23 53579727 53579727 + Silent SNP A A T TCGA-ED-A8O5-01A-11D-A35Z-10 TCGA-ED-A8O5-10A-01D-A35Z-10 g.chrX:53579727A>T c.8622T>A c.(8620-8622)acT>acA p.T2874T LIHC 23 53579842 53579842 + Missense_Mutation SNP G G T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chrX:53579842G>T c.8507C>A c.(8506-8508)cCa>cAa p.P2836Q LIHC 23 53591649 53591649 + Silent SNP A A G TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chrX:53591649A>G c.6915T>C c.(6913-6915)gaT>gaC p.D2305D LIHC 23 53591670 53591670 + Silent SNP T T C TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chrX:53591670T>C c.6894A>G c.(6892-6894)gaA>gaG p.E2298E LIHC 23 53603872 53603872 + Missense_Mutation SNP C C T TCGA-DD-AADW-01A-11D-A38X-10 TCGA-DD-AADW-10A-01D-A38X-10 g.chrX:53603872C>T c.5872G>A c.(5872-5874)Gct>Act p.A1958T LIHC 23 53617377 53617377 + Missense_Mutation SNP G G A TCGA-DD-AACH-01A-11D-A40R-10 TCGA-DD-AACH-10A-01D-A40U-10 g.chrX:53617377G>A c.4178C>T c.(4177-4179)gCa>gTa p.A1393V LIHC 23 53619443 53619443 + Missense_Mutation SNP T T A TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chrX:53619443T>A c.3887A>T c.(3886-3888)gAg>gTg p.E1296V LIHC 23 53630379 53630379 + Silent SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chrX:53630379A>G c.2826T>C c.(2824-2826)tgT>tgC p.C942C LIHC 23 53672263 53672263 + Splice_Site SNP C C T TCGA-DD-AAE2-01A-11D-A40R-10 TCGA-DD-AAE2-10A-01D-A40U-10 g.chrX:53672263C>T c.504G>A c.(502-504)gaG>gaA p.E168E LIHC 23 53672381 53672381 + Missense_Mutation SNP T T A TCGA-ED-A459-01A-11D-A25V-10 TCGA-ED-A459-10A-01D-A25V-10 g.chrX:53672381T>A c.386A>T c.(385-387)cAa>cTa p.Q129L LIHC 23 53674399 53674399 + Missense_Mutation SNP T T C TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chrX:53674399T>C c.263A>G c.(262-264)cAa>cGa p.Q88R LIHC 23 53674402 53674402 + Missense_Mutation SNP T T C TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chrX:53674402T>C c.260A>G c.(259-261)gAg>gGg p.E87G LIHC 23 53674404 53674404 + Silent SNP T T C TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chrX:53674404T>C c.258A>G c.(256-258)agA>agG p.R86R LUAD 23 53560323 53560323 + Frame_Shift_Del DEL G G - TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chrX:53560323delG c.13072delC c.(13072-13074)cacfs p.H4358fs LUAD 23 53560975 53560975 + Missense_Mutation SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chrX:53560975G>T c.13015C>A c.(13015-13017)Cac>Aac p.H4339N LUAD 23 53561122 53561122 + Missense_Mutation SNP G G T TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chrX:53561122G>T c.12868C>A c.(12868-12870)Caa>Aaa p.Q4290K LUAD 23 53563173 53563173 + Missense_Mutation SNP C C A TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chrX:53563173C>A c.12466G>T c.(12466-12468)Ggt>Tgt p.G4156C LUAD 23 53563335 53563339 + Splice_Site DEL CCTCA CCTCA - TCGA-97-8174-01A-11D-2284-08 TCGA-97-8174-10A-01D-2284-08 g.chrX:53563335_53563339delCCTCA c.e78+1 LUAD 23 53563456 53563456 + Missense_Mutation SNP G G C TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:53563456G>C c.12310C>G c.(12310-12312)Ctc>Gtc p.L4104V LUAD 23 53565946 53565946 + Frame_Shift_Del DEL G G - TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chrX:53565946delG c.11728delC c.(11728-11730)cacfs p.H3910fs LUAD 23 53566629 53566629 + Missense_Mutation SNP T T A TCGA-55-8090-01A-11D-2238-08 TCGA-55-8090-10A-01D-2238-08 g.chrX:53566629T>A c.11621A>T c.(11620-11622)cAt>cTt p.H3874L LUAD 23 53571562 53571562 + Missense_Mutation SNP G G T TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:53571562G>T c.11210C>A c.(11209-11211)aCg>aAg p.T3737K LUAD 23 53571671 53571671 + Missense_Mutation SNP C C A TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chrX:53571671C>A c.11101G>T c.(11101-11103)Ggt>Tgt p.G3701C LUAD 23 53571684 53571684 + Missense_Mutation SNP C C G TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chrX:53571684C>G c.11088G>C c.(11086-11088)caG>caC p.Q3696H LUAD 23 53571710 53571710 + Nonsense_Mutation SNP C C A TCGA-78-7147-01A-11D-2036-08 TCGA-78-7147-10A-01D-2036-08 g.chrX:53571710C>A c.11062G>T c.(11062-11064)Gag>Tag p.E3688* LUAD 23 53573739 53573739 + Missense_Mutation SNP C C A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chrX:53573739C>A c.10684G>T c.(10684-10686)Ggg>Tgg p.G3562W LUAD 23 53574724 53574724 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chrX:53574724C>A c.10546G>T c.(10546-10548)Gcc>Tcc p.A3516S LUAD 23 53574893 53574893 + Silent SNP G G C TCGA-97-A4M3-01A-11D-A24P-08 TCGA-97-A4M3-10A-01D-A24P-08 g.chrX:53574893G>C c.10377C>G c.(10375-10377)ctC>ctG p.L3459L LUAD 23 53576030 53576030 + Missense_Mutation SNP G G A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chrX:53576030G>A c.9925C>T c.(9925-9927)Cgt>Tgt p.R3309C LUAD 23 53577916 53577916 + Missense_Mutation SNP G G C TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chrX:53577916G>C c.9331C>G c.(9331-9333)Cgt>Ggt p.R3111G LUAD 23 53578038 53578038 + Missense_Mutation SNP C C A TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chrX:53578038C>A c.9209G>T c.(9208-9210)cGc>cTc p.R3070L LUAD 23 53578045 53578045 + Missense_Mutation SNP C C G TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chrX:53578045C>G c.9202G>C c.(9202-9204)Gac>Cac p.D3068H LUAD 23 53578103 53578103 + Silent SNP C C T TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chrX:53578103C>T c.9144G>A c.(9142-9144)caG>caA p.Q3048Q LUAD 23 53578301 53578301 + Missense_Mutation SNP C C A TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chrX:53578301C>A c.9022G>T c.(9022-9024)Gtg>Ttg p.V3008L LUAD 23 53578370 53578370 + Silent SNP G G A TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chrX:53578370G>A c.8953C>T c.(8953-8955)Cta>Tta p.L2985L LUAD 23 53578393 53578393 + Missense_Mutation SNP G G T TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chrX:53578393G>T c.8930C>A c.(8929-8931)cCt>cAt p.P2977H LUAD 23 53579703 53579703 + Missense_Mutation SNP C C G TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chrX:53579703C>G c.8646G>C c.(8644-8646)caG>caC p.Q2882H LUAD 23 53579742 53579742 + Silent SNP C C T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chrX:53579742C>T c.8607G>A c.(8605-8607)gaG>gaA p.E2869E LUAD 23 53581872 53581872 + Missense_Mutation SNP G G A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:53581872G>A c.8216C>T c.(8215-8217)cCt>cTt p.P2739L LUAD 23 53585705 53585705 + Missense_Mutation SNP C C G TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chrX:53585705C>G c.8071G>C c.(8071-8073)Gag>Cag p.E2691Q LUAD 23 53585707 53585707 + Missense_Mutation SNP C C A TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chrX:53585707C>A c.8069G>T c.(8068-8070)cGa>cTa p.R2690L LUAD 23 53591561 53591561 + Missense_Mutation SNP C C G TCGA-55-A493-01A-11D-A24D-08 TCGA-55-A493-10A-01D-A24F-08 g.chrX:53591561C>G c.7003G>C c.(7003-7005)Gag>Cag p.E2335Q LUAD 23 53591627 53591627 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chrX:53591627C>A c.6937G>T c.(6937-6939)Gtg>Ttg p.V2313L LUAD 23 53591666 53591666 + Missense_Mutation SNP C C G TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chrX:53591666C>G c.6898G>C c.(6898-6900)Gaa>Caa p.E2300Q LUAD 23 53596699 53596699 + Missense_Mutation SNP A A T TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chrX:53596699A>T c.6401T>A c.(6400-6402)cTg>cAg p.L2134Q LUAD 23 53596787 53596787 + Splice_Site SNP C C T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chrX:53596787C>T c.6313G>A c.(6313-6315)Gac>Aac p.D2105N LUAD 23 53607798 53607798 + Silent SNP T T A TCGA-73-4662-01A-01D-1265-08 TCGA-73-4662-11A-01D-1265-08 g.chrX:53607798T>A c.5709A>T c.(5707-5709)tcA>tcT p.S1903S LUAD 23 53607906 53607906 + Silent SNP G G T TCGA-55-7913-01B-11D-2238-08 TCGA-55-7913-10A-01D-2238-08 g.chrX:53607906G>T c.5601C>A c.(5599-5601)atC>atA p.I1867I LUAD 23 53610524 53610524 + Missense_Mutation SNP C C A TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chrX:53610524C>A c.5514G>T c.(5512-5514)atG>atT p.M1838I LUAD 23 53610529 53610529 + Missense_Mutation SNP T T C TCGA-50-5935-01A-11D-1753-08 TCGA-50-5935-11A-01D-1753-08 g.chrX:53610529T>C c.5509A>G c.(5509-5511)Acc>Gcc p.T1837A LUAD 23 53610740 53610740 + Silent SNP C C A TCGA-97-A4M3-01A-11D-A24P-08 TCGA-97-A4M3-10A-01D-A24P-08 g.chrX:53610740C>A c.5298G>T c.(5296-5298)ctG>ctT p.L1766L LUAD 23 53611279 53611279 + Silent SNP G G T TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chrX:53611279G>T c.5028C>A c.(5026-5028)cgC>cgA p.R1676R LUAD 23 53612061 53612061 + Missense_Mutation SNP T T C TCGA-91-7771-01A-11D-2167-08 TCGA-91-7771-10A-01D-2167-08 g.chrX:53612061T>C c.4912A>G c.(4912-4914)Att>Gtt p.I1638V LUAD 23 53616620 53616620 + Missense_Mutation SNP G G T TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chrX:53616620G>T c.4348C>A c.(4348-4350)Ctt>Att p.L1450I LUAD 23 53616745 53616745 + Missense_Mutation SNP C C A TCGA-MP-A4T7-01A-11D-A24P-08 TCGA-MP-A4T7-10A-01D-A24P-08 g.chrX:53616745C>A c.4223G>T c.(4222-4224)cGg>cTg p.R1408L LUAD 23 53617988 53617988 + Missense_Mutation SNP G G T TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chrX:53617988G>T c.4067C>A c.(4066-4068)cCt>cAt p.P1356H LUAD 23 53621555 53621555 + Missense_Mutation SNP C C T TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chrX:53621555C>T c.3407G>A c.(3406-3408)gGt>gAt p.G1136D LUAD 23 53629547 53629547 + Silent SNP C C A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:53629547C>A c.2949G>T c.(2947-2949)acG>acT p.T983T LUAD 23 53634598 53634598 + Silent SNP C C T TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chrX:53634598C>T c.2382G>A c.(2380-2382)gtG>gtA p.V794V LUAD 23 53634608 53634608 + Missense_Mutation SNP T T A TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chrX:53634608T>A c.2372A>T c.(2371-2373)cAg>cTg p.Q791L LUAD 23 53641508 53641508 + Missense_Mutation SNP C C G TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chrX:53641508C>G c.2248G>C c.(2248-2250)Gag>Cag p.E750Q LUAD 23 53641577 53641577 + Missense_Mutation SNP T T A TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chrX:53641577T>A c.2179A>T c.(2179-2181)Agt>Tgt p.S727C LUAD 23 53642720 53642720 + Silent SNP C C A TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chrX:53642720C>A c.2034G>T c.(2032-2034)acG>acT p.T678T LUAD 23 53643940 53643940 + Missense_Mutation SNP C C T TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chrX:53643940C>T c.1948G>A c.(1948-1950)Gat>Aat p.D650N LUAD 23 53644083 53644083 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chrX:53644083C>A c.1805G>T c.(1804-1806)gGc>gTc p.G602V LUAD 23 53644371 53644371 + Missense_Mutation SNP G G A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chrX:53644371G>A c.1709C>T c.(1708-1710)cCa>cTa p.P570L LUAD 23 53652124 53652124 + Nonsense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chrX:53652124G>A c.1585C>T c.(1585-1587)Cga>Tga p.R529* LUAD 23 53655812 53655812 + Silent SNP G G C TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chrX:53655812G>C c.1005C>G c.(1003-1005)gtC>gtG p.V335V LUAD 23 53661217 53661217 + Missense_Mutation SNP C C T TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chrX:53661217C>T c.538G>A c.(538-540)Gca>Aca p.A180T LUAD 23 53672299 53672299 + Missense_Mutation SNP C C G TCGA-50-6595-01A-12D-1855-08 TCGA-50-6595-11A-01D-1855-08 g.chrX:53672299C>G c.468G>C c.(466-468)agG>agC p.R156S LUAD 23 53672342 53672342 + Missense_Mutation SNP C C G TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chrX:53672342C>G c.425G>C c.(424-426)aGc>aCc p.S142T LUAD 23 53674396 53674396 + Missense_Mutation SNP A A T TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chrX:53674396A>T c.266T>A c.(265-267)cTg>cAg p.L89Q LUAD 23 53675171 53675171 + Missense_Mutation SNP G G A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chrX:53675171G>A c.128C>T c.(127-129)aCa>aTa p.T43I LUSC 23 53563496 53563496 + Silent SNP G G A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chrX:53563496G>A c.12270C>T c.(12268-12270)acC>acT p.T4090T LUSC 23 53564623 53564623 + Missense_Mutation SNP C C A TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chrX:53564623C>A c.12031G>T c.(12031-12033)Ggg>Tgg p.G4011W LUSC 23 53573708 53573708 + Missense_Mutation SNP A A T TCGA-60-2710-01A-01D-1522-08 TCGA-60-2710-11A-01D-1522-08 g.chrX:53573708A>T c.10715T>A c.(10714-10716)gTg>gAg p.V3572E LUSC 23 53574675 53574675 + Missense_Mutation SNP G G T TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chrX:53574675G>T c.10595C>A c.(10594-10596)aCc>aAc p.T3532N LUSC 23 53574688 53574689 + Missense_Mutation DNP CG CG AA TCGA-21-1070-01A-01D-1521-08 TCGA-21-1070-11A-01D-1521-08 g.chrX:53574688_53574689CG>AA c.10581_10582CG>TT c.(10579-10584)gtCGta>gtTTta p.V3528L LUSC 23 53574823 53574823 + Missense_Mutation SNP T T C TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chrX:53574823T>C c.10447A>G c.(10447-10449)Acc>Gcc p.T3483A LUSC 23 53578044 53578044 + Missense_Mutation SNP T T C TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chrX:53578044T>C c.9203A>G c.(9202-9204)gAc>gGc p.D3068G LUSC 23 53578078 53578078 + Missense_Mutation SNP C C A TCGA-46-6025-01A-11D-1817-08 TCGA-46-6025-10A-01D-1817-08 g.chrX:53578078C>A c.9169G>T c.(9169-9171)Gac>Tac p.D3057Y LUSC 23 53581603 53581603 + Missense_Mutation SNP G G C TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chrX:53581603G>C c.8485C>G c.(8485-8487)Ccc>Gcc p.P2829A LUSC 23 53584372 53584372 + Nonsense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chrX:53584372G>C c.8177C>G c.(8176-8178)tCa>tGa p.S2726* LUSC 23 53587154 53587154 + Silent SNP C C A TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chrX:53587154C>A c.7731G>T c.(7729-7731)ctG>ctT p.L2577L LUSC 23 53592131 53592131 + Missense_Mutation SNP C C G TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chrX:53592131C>G c.6777G>C c.(6775-6777)caG>caC p.Q2259H LUSC 23 53596671 53596671 + Silent SNP C C A TCGA-60-2710-01A-01D-1522-08 TCGA-60-2710-11A-01D-1522-08 g.chrX:53596671C>A c.6429G>T c.(6427-6429)ggG>ggT p.G2143G LUSC 23 53610791 53610791 + Silent SNP G G T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chrX:53610791G>T c.5247C>A c.(5245-5247)ggC>ggA p.G1749G LUSC 23 53611204 53611204 + Missense_Mutation SNP C C A TCGA-34-5232-01A-21D-1817-08 TCGA-34-5232-10A-01D-1817-08 g.chrX:53611204C>A c.5103G>T c.(5101-5103)gaG>gaT p.E1701D LUSC 23 53616585 53616585 + Silent SNP C C A TCGA-60-2720-01A-01D-1522-08 TCGA-60-2720-11A-01D-1522-08 g.chrX:53616585C>A c.4383G>T c.(4381-4383)gtG>gtT p.V1461V LUSC 23 53634648 53634648 + Missense_Mutation SNP C C T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chrX:53634648C>T c.2332G>A c.(2332-2334)Gaa>Aaa p.E778K LUSC 23 53641579 53641579 + Missense_Mutation SNP G G C TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chrX:53641579G>C c.2177C>G c.(2176-2178)tCt>tGt p.S726C LUSC 23 53642764 53642764 + Missense_Mutation SNP C C T TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chrX:53642764C>T c.1990G>A c.(1990-1992)Gat>Aat p.D664N LUSC 23 53659447 53659447 + Missense_Mutation SNP C C T TCGA-66-2800-01A-01D-1267-08 TCGA-66-2800-11A-01D-1267-08 g.chrX:53659447C>T c.637G>A c.(637-639)Gag>Aag p.E213K LUSC 23 53661239 53661240 + Missense_Mutation DNP TC TC AA TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chrX:53661239_53661240TC>AA c.515_516GA>TT c.(514-516)gGA>gTT p.G172V LUSC 23 53674517 53674517 + Splice_Site SNP A A G TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chrX:53674517A>G c.145T>C c.(145-147)Tgc>Cgc p.C49R OV 23 53563449 53563449 + Missense_Mutation SNP T T A TCGA-61-1907-01A-01W-0639-09 TCGA-61-1907-11A-01W-0640-09 g.chrX:53563449T>A c.12317A>T c.(12316-12318)tAc>tTc p.Y4106F OV 23 53571652 53571652 + Missense_Mutation SNP A A T TCGA-10-0926-01A-01W-0420-08 TCGA-10-0926-11A-01D-0399-08 g.chrX:53571652A>T c.11120T>A c.(11119-11121)cTg>cAg p.L3707Q OV 23 53576264 53576264 + Missense_Mutation SNP G G T TCGA-29-1777-01A-01W-0639-09 TCGA-29-1777-10A-01W-0639-09 g.chrX:53576264G>T c.9691C>A c.(9691-9693)Cag>Aag p.Q3231K OV 23 53577911 53577911 + Silent SNP C C G TCGA-13-0885-01A-02W-0421-09 TCGA-13-0885-10A-01W-0421-09 g.chrX:53577911C>G c.9336G>C c.(9334-9336)ctG>ctC p.L3112L OV 23 53577921 53577921 + Missense_Mutation SNP T T C TCGA-36-1577-01A-01W-0615-10 TCGA-36-1577-10A-01W-0615-10 g.chrX:53577921T>C c.9326A>G c.(9325-9327)cAt>cGt p.H3109R OV 23 53578127 53578127 + Missense_Mutation SNP C C A TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chrX:53578127C>A c.9120G>T c.(9118-9120)gaG>gaT p.E3040D OV 23 53578151 53578151 + Splice_Site SNP C C A TCGA-13-0887-01A-01W-0421-09 TCGA-13-0887-10A-01W-0421-09 g.chrX:53578151C>A c.e64-1 OV 23 53579651 53579651 + Missense_Mutation SNP C C T TCGA-61-2097-01A-02W-0722-08 TCGA-61-2097-11A-01W-0723-08 g.chrX:53579651C>T c.8698G>A c.(8698-8700)Gtg>Atg p.V2900M OV 23 53602136 53602136 + Missense_Mutation SNP A A G TCGA-24-1614-01A-01W-0552-10 TCGA-24-1614-10A-01W-0552-10 g.chrX:53602136A>G c.6076T>C c.(6076-6078)Tct>Cct p.S2026P OV 23 53607799 53607799 + Nonsense_Mutation SNP G G C TCGA-09-2050-01A-01W-0799-08 TCGA-09-2050-10A-01W-0799-08 g.chrX:53607799G>C c.5708C>G c.(5707-5709)tCa>tGa p.S1903* OV 23 53612055 53612055 + Missense_Mutation SNP A A T TCGA-13-0886-01A-01W-0420-08 TCGA-13-0886-10A-01D-0399-08 g.chrX:53612055A>T c.4918T>A c.(4918-4920)Tct>Act p.S1640T OV 23 53622190 53622190 + Silent SNP A A G TCGA-29-1691-01A-01W-0633-09 TCGA-29-1691-10A-01W-0633-09 g.chrX:53622190A>G c.3337T>C c.(3337-3339)Tta>Cta p.L1113L OV 23 53655545 53655545 + Missense_Mutation SNP G G T TCGA-25-1630-01A-01W-0615-10 TCGA-25-1630-10A-01W-0615-10 g.chrX:53655545G>T c.1141C>A c.(1141-1143)Cag>Aag p.Q381K OV 23 53672376 53672376 + Missense_Mutation SNP C C A TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chrX:53672376C>A c.391G>T c.(391-393)Gtg>Ttg p.V131L PAAD 23 53566769 53566769 + Silent SNP G G T TCGA-LB-A9Q5-01A-11D-A397-08 TCGA-LB-A9Q5-10A-01D-A39A-08 g.chrX:53566769G>T c.11481C>A c.(11479-11481)tcC>tcA p.S3827S PAAD 23 53575044 53575044 + Missense_Mutation SNP T T A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:53575044T>A c.10226A>T c.(10225-10227)aAg>aTg p.K3409M PAAD 23 53579602 53579602 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:53579602T>C c.8747A>G c.(8746-8748)gAc>gGc p.D2916G PAAD 23 53631738 53631738 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:53631738G>A c.2554C>T c.(2554-2556)Ctc>Ttc p.L852F PAAD 23 53674485 53674485 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:53674485G>A c.177C>T c.(175-177)gaC>gaT p.D59D PCPG 23 53570843 53570843 + Missense_Mutation SNP G G A TCGA-QR-A70A-01A-11D-A35D-08 TCGA-QR-A70A-10A-01D-A35B-08 g.chrX:53570843G>A c.11338C>T c.(11338-11340)Cgt>Tgt p.R3780C PCPG 23 53588818 53588818 + Missense_Mutation SNP T T C TCGA-QR-A70E-01A-11D-A35D-08 TCGA-QR-A70E-10A-01D-A35B-08 g.chrX:53588818T>C c.7406A>G c.(7405-7407)gAg>gGg p.E2469G PCPG 23 53602646 53602646 + Missense_Mutation SNP C C A TCGA-SP-A6QJ-01A-11D-A35I-08 TCGA-SP-A6QJ-10A-01D-A35G-08 g.chrX:53602646C>A c.5987G>T c.(5986-5988)cGt>cTt p.R1996L PRAD 23 53561001 53561001 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chrX:53561001C>A c.12989G>T c.(12988-12990)aGg>aTg p.R4330M PRAD 23 53563401 53563401 + Missense_Mutation SNP C C T TCGA-VN-A88O-01A-11D-A34U-08 TCGA-VN-A88O-10A-01D-A34X-08 g.chrX:53563401C>T c.12365G>A c.(12364-12366)cGt>cAt p.R4122H PRAD 23 53576284 53576284 + Missense_Mutation SNP C C A TCGA-ZG-A8QZ-01A-11D-A377-08 TCGA-ZG-A8QZ-10A-01D-A37A-08 g.chrX:53576284C>A c.9671G>T c.(9670-9672)cGc>cTc p.R3224L PRAD 23 53578098 53578098 + Missense_Mutation SNP G G A TCGA-QU-A6IM-01A-11D-A31L-08 TCGA-QU-A6IM-10A-01D-A31J-08 g.chrX:53578098G>A c.9149C>T c.(9148-9150)gCc>gTc p.A3050V PRAD 23 53586378 53586378 + Missense_Mutation SNP G G C TCGA-XK-AAJT-01A-11D-A41K-08 TCGA-XK-AAJT-10A-01D-A41N-08 g.chrX:53586378G>C c.7852C>G c.(7852-7854)Cgt>Ggt p.R2618G PRAD 23 53618049 53618049 + Missense_Mutation SNP T T C TCGA-G9-7510-01A-11D-2260-08 TCGA-G9-7510-10A-01D-2260-08 g.chrX:53618049T>C c.4006A>G c.(4006-4008)Atg>Gtg p.M1336V PRAD 23 53620387 53620387 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chrX:53620387C>T c.3678G>A c.(3676-3678)ttG>ttA p.L1226L PRAD 23 53621471 53621471 + Missense_Mutation SNP T T C TCGA-ZG-A9L5-01A-12D-A41K-08 TCGA-ZG-A9L5-10A-01D-A41N-08 g.chrX:53621471T>C c.3491A>G c.(3490-3492)aAt>aGt p.N1164S PRAD 23 53657925 53657925 + Missense_Mutation SNP T T C TCGA-EJ-5508-01A-02D-1576-08 TCGA-EJ-5508-10A-01D-1577-08 g.chrX:53657925T>C c.824A>G c.(823-825)cAg>cGg p.Q275R READ 23 53561010 53561010 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:53561010C>T c.12980G>A c.(12979-12981)cGa>cAa p.R4327Q READ 23 53565406 53565406 + Missense_Mutation SNP C C T TCGA-AG-A020-01A-21W-A096-10 TCGA-AG-A020-11A-11W-A096-10 g.chrX:53565406C>T c.11888G>A c.(11887-11889)cGc>cAc p.R3963H READ 23 53574917 53574917 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:53574917C>A c.10353G>T c.(10351-10353)gaG>gaT p.E3451D READ 23 53610679 53610679 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chrX:53610679G>A c.5359C>T c.(5359-5361)Cgg>Tgg p.R1787W READ 23 53616547 53616547 + Missense_Mutation SNP G G C TCGA-DY-A1DF-01A-11D-A152-10 TCGA-DY-A1DF-10A-01D-A152-10 g.chrX:53616547G>C c.4421C>G c.(4420-4422)gCa>gGa p.A1474G READ 23 53642763 53642763 + Missense_Mutation SNP T T A TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chrX:53642763T>A c.1991A>T c.(1990-1992)gAt>gTt p.D664V SARC 23 53573735 53573735 + Missense_Mutation SNP C C G TCGA-IE-A4EI-01A-11D-A24N-09 TCGA-IE-A4EI-10A-01D-A24N-09 g.chrX:53573735C>G c.10688G>C c.(10687-10689)gGc>gCc p.G3563A SARC 23 53589091 53589093 + In_Frame_Del DEL TCC TCC - TCGA-MB-A8JK-01A-11D-A36J-09 TCGA-MB-A8JK-10A-01D-A36M-09 g.chrX:53589091_53589093delTCC c.7317_7319delGGA c.(7315-7320)gaggaa>gaa p.2439_2440EE>E SARC 23 53619440 53619440 + Missense_Mutation SNP C C T TCGA-PC-A5DO-01A-11D-A26G-09 TCGA-PC-A5DO-10A-01D-A26G-09 g.chrX:53619440C>T c.3890G>A c.(3889-3891)gGg>gAg p.G1297E SARC 23 53620560 53620560 + Splice_Site SNP T T C TCGA-K1-A3PN-01A-11D-A228-09 TCGA-K1-A3PN-10A-01D-A22A-09 g.chrX:53620560T>C c.3505A>G c.(3505-3507)Act>Gct p.T1169A SARC 23 53631666 53631666 + Missense_Mutation SNP A A G TCGA-DX-A8BM-01A-11D-A417-09 TCGA-DX-A8BM-10B-01D-A41A-09 g.chrX:53631666A>G c.2626T>C c.(2626-2628)Tgc>Cgc p.C876R SKCM 23 53563540 53563540 + Missense_Mutation SNP G G A TCGA-D9-A6EA-06A-11D-A30X-08 TCGA-D9-A6EA-10A-01D-A30X-08 g.chrX:53563540G>A c.12226C>T c.(12226-12228)Cct>Tct p.P4076S SKCM 23 53563559 53563559 + Silent SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chrX:53563559G>A c.12207C>T c.(12205-12207)atC>atT p.I4069I SKCM 23 53564554 53564554 + Silent SNP G G A TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chrX:53564554G>A c.12100C>T c.(12100-12102)Ctg>Ttg p.L4034L SKCM 23 53565956 53565956 + Silent SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chrX:53565956G>A c.11718C>T c.(11716-11718)agC>agT p.S3906S SKCM 23 53566728 53566728 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chrX:53566728G>A c.11522C>T c.(11521-11523)cCa>cTa p.P3841L SKCM 23 53566768 53566768 + Missense_Mutation SNP C C A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:53566768C>A c.11482G>T c.(11482-11484)Gat>Tat p.D3828Y SKCM 23 53573412 53573412 + Missense_Mutation SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chrX:53573412G>A c.10900C>T c.(10900-10902)Ctt>Ttt p.L3634F SKCM 23 53573714 53573714 + Missense_Mutation SNP T T C TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chrX:53573714T>C c.10709A>G c.(10708-10710)aAg>aGg p.K3570R SKCM 23 53574783 53574785 + In_Frame_Del DEL GTG GTG - TCGA-EE-A29A-06A-12D-A196-08 TCGA-EE-A29A-10A-01D-A198-08 g.chrX:53574783_53574785delGTG c.10485_10487delCAC c.(10483-10488)accact>act p.3495_3496TT>T SKCM 23 53575230 53575230 + Missense_Mutation SNP A A T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chrX:53575230A>T c.10040T>A c.(10039-10041)tTt>tAt p.F3347Y SKCM 23 53576162 53576162 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chrX:53576162C>T c.9793G>A c.(9793-9795)Gag>Aag p.E3265K SKCM 23 53576271 53576271 + Silent SNP G G A TCGA-ER-A19M-06A-61D-A23B-08 TCGA-ER-A19M-10A-01D-A23B-08 g.chrX:53576271G>A c.9684C>T c.(9682-9684)tcC>tcT p.S3228S SKCM 23 53577633 53577633 + Missense_Mutation SNP T T C TCGA-FS-A4FB-06A-11D-A25O-08 TCGA-FS-A4FB-10B-01D-A25O-08 g.chrX:53577633T>C c.9482A>G c.(9481-9483)cAt>cGt p.H3161R SKCM 23 53581619 53581619 + Missense_Mutation SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chrX:53581619C>T c.8469G>A c.(8467-8469)atG>atA p.M2823I SKCM 23 53581758 53581758 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:53581758G>A c.8330C>T c.(8329-8331)cCa>cTa p.P2777L SKCM 23 53585694 53585694 + Silent SNP C C T TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chrX:53585694C>T c.8082G>A c.(8080-8082)agG>agA p.R2694R SKCM 23 53592178 53592178 + Missense_Mutation SNP T T C TCGA-D3-A2JC-06A-11D-A19A-08 TCGA-D3-A2JC-10A-01D-A19A-08 g.chrX:53592178T>C c.6730A>G c.(6730-6732)Aat>Gat p.N2244D SKCM 23 53595718 53595718 + Missense_Mutation SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chrX:53595718C>T c.6641G>A c.(6640-6642)cGg>cAg p.R2214Q SKCM 23 53600725 53600725 + Silent SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chrX:53600725A>G c.6297T>C c.(6295-6297)tcT>tcC p.S2099S SKCM 23 53600921 53600921 + Missense_Mutation SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chrX:53600921G>A c.6101C>T c.(6100-6102)tCa>tTa p.S2034L SKCM 23 53610870 53610870 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:53610870G>A c.5168C>T c.(5167-5169)cCt>cTt p.P1723L SKCM 23 53611302 53611302 + Missense_Mutation SNP T T C TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chrX:53611302T>C c.5005A>G c.(5005-5007)Aat>Gat p.N1669D SKCM 23 53613787 53613787 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:53613787G>A c.4697C>T c.(4696-4698)cCc>cTc p.P1566L SKCM 23 53616539 53616539 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chrX:53616539G>A c.4429C>T c.(4429-4431)Cgt>Tgt p.R1477C SKCM 23 53617393 53617393 + Missense_Mutation SNP G G A TCGA-D3-A1QB-06A-11D-A19A-08 TCGA-D3-A1QB-10A-01D-A19A-08 g.chrX:53617393G>A c.4162C>T c.(4162-4164)Cca>Tca p.P1388S SKCM 23 53617456 53617456 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:53617456G>A c.4099C>T c.(4099-4101)Ctc>Ttc p.L1367F SKCM 23 53619423 53619423 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chrX:53619423C>T c.3907G>A c.(3907-3909)Gat>Aat p.D1303N SKCM 23 53620471 53620471 + Silent SNP G G A TCGA-FS-A1YW-06A-11D-A197-08 TCGA-FS-A1YW-10A-01D-A199-08 g.chrX:53620471G>A c.3594C>T c.(3592-3594)ttC>ttT p.F1198F SKCM 23 53621488 53621488 + Silent SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chrX:53621488G>A c.3474C>T c.(3472-3474)ctC>ctT p.L1158L SKCM 23 53622156 53622156 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chrX:53622156G>A c.3371C>T c.(3370-3372)cCc>cTc p.P1124L SKCM 23 53630443 53630443 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:53630443G>A c.2762C>T c.(2761-2763)tCc>tTc p.S921F SKCM 23 53631699 53631699 + Missense_Mutation SNP G G A TCGA-EE-A29C-06A-21D-A197-08 TCGA-EE-A29C-10A-01D-A199-08 g.chrX:53631699G>A c.2593C>T c.(2593-2595)Cct>Tct p.P865S SKCM 23 53642793 53642793 + Missense_Mutation SNP T T G TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chrX:53642793T>G c.1961A>C c.(1960-1962)gAt>gCt p.D654A SKCM 23 53642794 53642794 + Missense_Mutation SNP C C T TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chrX:53642794C>T c.1960G>A c.(1960-1962)Gat>Aat p.D654N SKCM 23 53643934 53643934 + Missense_Mutation SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chrX:53643934G>A c.1954C>T c.(1954-1956)Ctt>Ttt p.L652F SKCM 23 53652121 53652121 + Missense_Mutation SNP G G C TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chrX:53652121G>C c.1588C>G c.(1588-1590)Cat>Gat p.H530D SKCM 23 53652212 53652212 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chrX:53652212C>G c.1497G>C c.(1495-1497)caG>caC p.Q499H SKCM 23 53654416 53654416 + Silent SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chrX:53654416C>T c.1434G>A c.(1432-1434)aaG>aaA p.K478K SKCM 23 53654425 53654425 + Silent SNP G G A TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chrX:53654425G>A c.1425C>T c.(1423-1425)atC>atT p.I475I SKCM 23 53654436 53654436 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:53654436G>A c.1414C>T c.(1414-1416)Ccg>Tcg p.P472S SKCM 23 53657952 53657952 + Missense_Mutation SNP C C T TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chrX:53657952C>T c.797G>A c.(796-798)gGc>gAc p.G266D SKCM 23 53674318 53674318 + Missense_Mutation SNP G G A TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chrX:53674318G>A c.344C>T c.(343-345)tCc>tTc p.S115F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US X 53619497 53619497 single base substitution C T missense_variant C1278Y 3833G>A ALL-US X 53619497 53619497 single base substitution C T missense_variant C311Y 932G>A BLCA-CN X 53576095 53576095 single base substitution G A missense_variant S124L 371C>T BLCA-CN X 53576095 53576095 single base substitution G A missense_variant S2320L 6959C>T BLCA-CN X 53576095 53576095 single base substitution G A missense_variant S3287L 9860C>T BLCA-CN X 53576095 53576095 single base substitution G A upstream_gene_variant BLCA-CN X 53576355 53576355 single base substitution G A synonymous_variant L2233L 6699C>T BLCA-CN X 53576355 53576355 single base substitution G A synonymous_variant L3200L 9600C>T BLCA-CN X 53576355 53576355 single base substitution G A synonymous_variant L37L 111C>T BLCA-CN X 53576355 53576355 single base substitution G A upstream_gene_variant BLCA-CN X 53585645 53585645 single base substitution C T missense_variant D1744N 5230G>A BLCA-CN X 53585645 53585645 single base substitution C T missense_variant D2711N 8131G>A BLCA-CN X 53619381 53619381 single base substitution C T missense_variant V1317I 3949G>A BLCA-CN X 53619381 53619381 single base substitution C T missense_variant V350I 1048G>A BLCA-US X 53575134 53575134 single base substitution G A missense_variant S216F 647C>T BLCA-US X 53575134 53575134 single base substitution G A missense_variant S2412F 7235C>T BLCA-US X 53575134 53575134 single base substitution G A missense_variant S3379F 10136C>T BLCA-US X 53575134 53575134 single base substitution G A upstream_gene_variant BLCA-US X 53578103 53578103 single base substitution C T synonymous_variant Q2081Q 6243G>A BLCA-US X 53578103 53578103 single base substitution C T synonymous_variant Q3048Q 9144G>A BLCA-US X 53578103 53578103 single base substitution C T upstream_gene_variant BLCA-US X 53578136 53578136 single base substitution C G missense_variant Q2070H 6210G>C BLCA-US X 53578136 53578136 single base substitution C G missense_variant Q3037H 9111G>C BLCA-US X 53578136 53578136 single base substitution C G upstream_gene_variant BLCA-US X 53578272 53578272 single base substitution C G synonymous_variant V2050V 6150G>C BLCA-US X 53578272 53578272 single base substitution C G synonymous_variant V3017V 9051G>C BLCA-US X 53578272 53578272 single base substitution C G upstream_gene_variant BLCA-US X 53587226 53587226 single base substitution C T synonymous_variant L1586L 4758G>A BLCA-US X 53587226 53587226 single base substitution C T synonymous_variant L2553L 7659G>A BLCA-US X 53603879 53603879 single base substitution T C synonymous_variant A1955A 5865A>G BLCA-US X 53603879 53603879 single base substitution T C synonymous_variant A988A 2964A>G BLCA-US X 53617425 53617425 single base substitution C G missense_variant R1377T 4130G>C BLCA-US X 53617425 53617425 single base substitution C G missense_variant R410T 1229G>C BLCA-US X 53620499 53620499 single base substitution G C stop_gained S1189* 3566C>G BLCA-US X 53620499 53620499 single base substitution G C stop_gained S222* 665C>G BLCA-US X 53631583 53631583 single base substitution G C missense_variant I903M 2709C>G BLCA-US X 53631583 53631583 single base substitution G C upstream_gene_variant BLCA-US X 53655540 53655540 deletion of <=200bp A - downstream_gene_variant BLCA-US X 53655540 53655540 deletion of <=200bp A - frameshift_variant F382 BLCA-US X 53655540 53655540 deletion of <=200bp A - upstream_gene_variant BLCA-US X 53672365 53672365 single base substitution G A downstream_gene_variant BLCA-US X 53672365 53672365 single base substitution G A synonymous_variant V134V 402C>T BOCA-FR X 53688745 53688745 single base substitution T A intron_variant BRCA-EU X 53554458 53554458 single base substitution C T downstream_gene_variant BRCA-EU X 53554824 53554824 single base substitution C T downstream_gene_variant BRCA-EU X 53556726 53556726 single base substitution C A downstream_gene_variant BRCA-EU X 53557378 53557378 single base substitution T C downstream_gene_variant BRCA-EU X 53557582 53557582 single base substitution G C downstream_gene_variant BRCA-EU X 53558064 53558064 single base substitution C G downstream_gene_variant BRCA-EU X 53558957 53558957 single base substitution T G downstream_gene_variant BRCA-EU X 53559876 53559876 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU X 53559876 53559876 deletion of <=200bp A - downstream_gene_variant BRCA-EU X 53560237 53560237 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU X 53560237 53560237 insertion of <=200bp - A downstream_gene_variant BRCA-EU X 53560716 53560716 single base substitution C G downstream_gene_variant BRCA-EU X 53560716 53560716 single base substitution C G exon_variant BRCA-EU X 53560716 53560716 single base substitution C G intron_variant BRCA-EU X 53561622 53561622 single base substitution C A downstream_gene_variant BRCA-EU X 53561622 53561622 single base substitution C A missense_variant G1051V 3152G>T BRCA-EU X 53561622 53561622 single base substitution C A missense_variant G3262V 9785G>T BRCA-EU X 53561622 53561622 single base substitution C A missense_variant G4229V 12686G>T BRCA-EU X 53561622 53561622 single base substitution C A upstream_gene_variant BRCA-EU X 53562251 53562251 single base substitution C T downstream_gene_variant BRCA-EU X 53562251 53562251 single base substitution C T intron_variant BRCA-EU X 53562251 53562251 single base substitution C T upstream_gene_variant BRCA-EU X 53562982 53562982 single base substitution G T downstream_gene_variant BRCA-EU X 53562982 53562982 single base substitution G T exon_variant BRCA-EU X 53562982 53562982 single base substitution G T intron_variant BRCA-EU X 53562982 53562982 single base substitution G T upstream_gene_variant BRCA-EU X 53564487 53564487 single base substitution G A downstream_gene_variant BRCA-EU X 53564487 53564487 single base substitution G A exon_variant BRCA-EU X 53564487 53564487 single base substitution G A intron_variant BRCA-EU X 53564487 53564487 single base substitution G A upstream_gene_variant BRCA-EU X 53564642 53564642 single base substitution C T downstream_gene_variant BRCA-EU X 53564642 53564642 single base substitution C T exon_variant BRCA-EU X 53564642 53564642 single base substitution C T synonymous_variant E3037E 9111G>A BRCA-EU X 53564642 53564642 single base substitution C T synonymous_variant E4004E 12012G>A BRCA-EU X 53564642 53564642 single base substitution C T synonymous_variant E826E 2478G>A BRCA-EU X 53564642 53564642 single base substitution C T upstream_gene_variant BRCA-EU X 53565311 53565311 single base substitution C G downstream_gene_variant BRCA-EU X 53565311 53565311 single base substitution C G exon_variant BRCA-EU X 53565311 53565311 single base substitution C G missense_variant D3028H 9082G>C BRCA-EU X 53565311 53565311 single base substitution C G missense_variant D3995H 11983G>C BRCA-EU X 53565311 53565311 single base substitution C G missense_variant D817H 2449G>C BRCA-EU X 53565311 53565311 single base substitution C G upstream_gene_variant BRCA-EU X 53565994 53565994 single base substitution G A downstream_gene_variant BRCA-EU X 53565994 53565994 single base substitution G A missense_variant R2927W 8779C>T BRCA-EU X 53565994 53565994 single base substitution G A missense_variant R3894W 11680C>T BRCA-EU X 53565994 53565994 single base substitution G A missense_variant R716W 2146C>T BRCA-EU X 53565994 53565994 single base substitution G A upstream_gene_variant BRCA-EU X 53566431 53566431 deletion of <=200bp C - downstream_gene_variant BRCA-EU X 53566431 53566431 deletion of <=200bp C - intron_variant BRCA-EU X 53566431 53566431 deletion of <=200bp C - upstream_gene_variant BRCA-EU X 53566846 53566846 single base substitution G A downstream_gene_variant BRCA-EU X 53566846 53566846 single base substitution G A intron_variant BRCA-EU X 53566846 53566846 single base substitution G A upstream_gene_variant BRCA-EU X 53567064 53567064 single base substitution C T downstream_gene_variant BRCA-EU X 53567064 53567064 single base substitution C T intron_variant BRCA-EU X 53567064 53567064 single base substitution C T upstream_gene_variant BRCA-EU X 53568669 53568669 single base substitution A T downstream_gene_variant BRCA-EU X 53568669 53568669 single base substitution A T intron_variant BRCA-EU X 53568669 53568669 single base substitution A T upstream_gene_variant BRCA-EU X 53568671 53568671 single base substitution A C downstream_gene_variant BRCA-EU X 53568671 53568671 single base substitution A C intron_variant BRCA-EU X 53568671 53568671 single base substitution A C upstream_gene_variant BRCA-EU X 53569469 53569469 single base substitution C T downstream_gene_variant BRCA-EU X 53569469 53569469 single base substitution C T exon_variant BRCA-EU X 53569469 53569469 single base substitution C T missense_variant R2837Q 8510G>A BRCA-EU X 53569469 53569469 single base substitution C T missense_variant R3804Q 11411G>A BRCA-EU X 53569469 53569469 single base substitution C T missense_variant R626Q 1877G>A BRCA-EU X 53569469 53569469 single base substitution C T upstream_gene_variant BRCA-EU X 53569497 53569497 single base substitution C G downstream_gene_variant BRCA-EU X 53569497 53569497 single base substitution C G exon_variant BRCA-EU X 53569497 53569497 single base substitution C G missense_variant E2828Q 8482G>C BRCA-EU X 53569497 53569497 single base substitution C G missense_variant E3795Q 11383G>C BRCA-EU X 53569497 53569497 single base substitution C G missense_variant E617Q 1849G>C BRCA-EU X 53569497 53569497 single base substitution C G upstream_gene_variant BRCA-EU X 53569498 53569498 single base substitution C T downstream_gene_variant BRCA-EU X 53569498 53569498 single base substitution C T exon_variant BRCA-EU X 53569498 53569498 single base substitution C T splice_region_variant BRCA-EU X 53569498 53569498 single base substitution C T upstream_gene_variant BRCA-EU X 53570824 53570824 single base substitution C T exon_variant BRCA-EU X 53570824 53570824 single base substitution C T intron_variant BRCA-EU X 53570824 53570824 single base substitution C T missense_variant R2819Q 8456G>A BRCA-EU X 53570824 53570824 single base substitution C T missense_variant R3786Q 11357G>A BRCA-EU X 53570824 53570824 single base substitution C T upstream_gene_variant BRCA-EU X 53572002 53572002 single base substitution T G exon_variant BRCA-EU X 53572002 53572002 single base substitution T G missense_variant K2712T 8135A>C BRCA-EU X 53572002 53572002 single base substitution T G missense_variant K3679T 11036A>C BRCA-EU X 53572002 53572002 single base substitution T G missense_variant K516T 1547A>C BRCA-EU X 53572002 53572002 single base substitution T G upstream_gene_variant BRCA-EU X 53572863 53572863 single base substitution C T intron_variant BRCA-EU X 53572863 53572863 single base substitution C T upstream_gene_variant BRCA-EU X 53573193 53573193 single base substitution C A intron_variant BRCA-EU X 53573193 53573193 single base substitution C A upstream_gene_variant BRCA-EU X 53573429 53573429 single base substitution C T exon_variant BRCA-EU X 53573429 53573429 single base substitution C T missense_variant R2661H 7982G>A BRCA-EU X 53573429 53573429 single base substitution C T missense_variant R3628H 10883G>A BRCA-EU X 53573429 53573429 single base substitution C T missense_variant R465H 1394G>A BRCA-EU X 53573429 53573429 single base substitution C T upstream_gene_variant BRCA-EU X 53573916 53573916 single base substitution C T intron_variant BRCA-EU X 53573916 53573916 single base substitution C T upstream_gene_variant BRCA-EU X 53574164 53574164 single base substitution C G intron_variant BRCA-EU X 53574164 53574164 single base substitution C G upstream_gene_variant BRCA-EU X 53575024 53575024 single base substitution C T missense_variant G2449S 7345G>A BRCA-EU X 53575024 53575024 single base substitution C T missense_variant G253S 757G>A BRCA-EU X 53575024 53575024 single base substitution C T missense_variant G3416S 10246G>A BRCA-EU X 53575024 53575024 single base substitution C T upstream_gene_variant BRCA-EU X 53577199 53577199 single base substitution A G intron_variant BRCA-EU X 53577199 53577199 single base substitution A G upstream_gene_variant BRCA-EU X 53577343 53577343 single base substitution C T intron_variant BRCA-EU X 53577343 53577343 single base substitution C T upstream_gene_variant BRCA-EU X 53578577 53578577 single base substitution C A intron_variant BRCA-EU X 53578577 53578577 single base substitution C A upstream_gene_variant BRCA-EU X 53579683 53579683 single base substitution G T missense_variant T1922N 5765C>A BRCA-EU X 53579683 53579683 single base substitution G T missense_variant T2889N 8666C>A BRCA-EU X 53579683 53579683 single base substitution G T upstream_gene_variant BRCA-EU X 53580167 53580167 single base substitution C G intron_variant BRCA-EU X 53580167 53580167 single base substitution C G upstream_gene_variant BRCA-EU X 53580173 53580173 single base substitution C T intron_variant BRCA-EU X 53580173 53580173 single base substitution C T upstream_gene_variant BRCA-EU X 53580395 53580395 single base substitution G C intron_variant BRCA-EU X 53580395 53580395 single base substitution G C upstream_gene_variant BRCA-EU X 53581189 53581189 deletion of <=200bp T - intron_variant BRCA-EU X 53581189 53581189 deletion of <=200bp T - upstream_gene_variant BRCA-EU X 53581327 53581327 single base substitution T C intron_variant BRCA-EU X 53581327 53581327 single base substitution T C upstream_gene_variant BRCA-EU X 53584218 53584218 single base substitution C T intron_variant BRCA-EU X 53584248 53584248 single base substitution C G intron_variant BRCA-EU X 53584286 53584286 single base substitution C G intron_variant BRCA-EU X 53586669 53586669 single base substitution A C intron_variant BRCA-EU X 53586874 53586874 single base substitution G T intron_variant BRCA-EU X 53587091 53587091 single base substitution A C intron_variant BRCA-EU X 53587127 53587127 single base substitution C A intron_variant BRCA-EU X 53590186 53590186 single base substitution C T intron_variant BRCA-EU X 53590567 53590567 single base substitution C A intron_variant BRCA-EU X 53591850 53591850 single base substitution C A intron_variant BRCA-EU X 53591937 53591937 single base substitution A C intron_variant BRCA-EU X 53592886 53592886 single base substitution A G intron_variant BRCA-EU X 53594854 53594854 single base substitution A G intron_variant BRCA-EU X 53597187 53597187 single base substitution T C intron_variant BRCA-EU X 53597305 53597305 single base substitution T G intron_variant BRCA-EU X 53597329 53597329 single base substitution G A intron_variant BRCA-EU X 53599321 53599321 single base substitution C T intron_variant BRCA-EU X 53599570 53599570 single base substitution G C intron_variant BRCA-EU X 53599985 53599985 single base substitution C G intron_variant BRCA-EU X 53600420 53600420 single base substitution C T intron_variant BRCA-EU X 53601404 53601404 single base substitution G A intron_variant BRCA-EU X 53601741 53601741 single base substitution G T intron_variant BRCA-EU X 53602284 53602284 single base substitution C G intron_variant BRCA-EU X 53602714 53602714 single base substitution G T synonymous_variant T1006T 3018C>A BRCA-EU X 53602714 53602714 single base substitution G T synonymous_variant T1973T 5919C>A BRCA-EU X 53602845 53602845 single base substitution C G intron_variant BRCA-EU X 53609242 53609242 single base substitution C G downstream_gene_variant BRCA-EU X 53609242 53609242 single base substitution C G intron_variant BRCA-EU X 53610717 53610717 single base substitution G A downstream_gene_variant BRCA-EU X 53610717 53610717 single base substitution G A missense_variant T1774I 5321C>T BRCA-EU X 53610717 53610717 single base substitution G A missense_variant T807I 2420C>T BRCA-EU X 53611416 53611416 single base substitution C A intron_variant BRCA-EU X 53611745 53611745 single base substitution T G intron_variant BRCA-EU X 53614171 53614171 single base substitution T A intron_variant BRCA-EU X 53614834 53614834 single base substitution C G intron_variant BRCA-EU X 53615025 53615025 single base substitution A T intron_variant BRCA-EU X 53615171 53615171 single base substitution G A intron_variant BRCA-EU X 53615201 53615201 single base substitution C A intron_variant BRCA-EU X 53615546 53615546 single base substitution T G intron_variant BRCA-EU X 53615595 53615595 single base substitution C A intron_variant BRCA-EU X 53615831 53615832 deletion of <=200bp TC - intron_variant BRCA-EU X 53616165 53616165 single base substitution C A intron_variant BRCA-EU X 53616181 53616181 single base substitution C A intron_variant BRCA-EU X 53616589 53616589 single base substitution C T missense_variant R1460H 4379G>A BRCA-EU X 53616589 53616589 single base substitution C T missense_variant R493H 1478G>A BRCA-EU X 53616752 53616752 single base substitution C G missense_variant E1406Q 4216G>C BRCA-EU X 53616752 53616752 single base substitution C G missense_variant E439Q 1315G>C BRCA-EU X 53617021 53617021 single base substitution C T intron_variant BRCA-EU X 53618198 53618198 single base substitution G T intron_variant BRCA-EU X 53619325 53619325 single base substitution T C intron_variant BRCA-EU X 53620639 53620639 single base substitution C A intron_variant BRCA-EU X 53621057 53621057 insertion of <=200bp - A intron_variant BRCA-EU X 53626463 53626463 deletion of <=200bp A - intron_variant BRCA-EU X 53626468 53626468 single base substitution A C intron_variant BRCA-EU X 53628215 53628215 single base substitution C T intron_variant BRCA-EU X 53628265 53628265 single base substitution C A intron_variant BRCA-EU X 53628457 53628457 single base substitution T A intron_variant BRCA-EU X 53628497 53628497 deletion of <=200bp T - intron_variant BRCA-EU X 53629539 53629539 single base substitution C G intron_variant BRCA-EU X 53629539 53629539 single base substitution C G missense_variant G986A 2957G>C BRCA-EU X 53630412 53630412 single base substitution C G synonymous_variant L931L 2793G>C BRCA-EU X 53630412 53630412 single base substitution C G upstream_gene_variant BRCA-EU X 53630995 53630995 single base substitution C G intron_variant BRCA-EU X 53630995 53630995 single base substitution C G upstream_gene_variant BRCA-EU X 53632065 53632065 single base substitution G A intron_variant BRCA-EU X 53632065 53632065 single base substitution G A upstream_gene_variant BRCA-EU X 53632342 53632342 single base substitution T C intron_variant BRCA-EU X 53632342 53632342 single base substitution T C upstream_gene_variant BRCA-EU X 53632379 53632379 single base substitution G C intron_variant BRCA-EU X 53632379 53632379 single base substitution G C upstream_gene_variant BRCA-EU X 53632560 53632560 single base substitution G C intron_variant BRCA-EU X 53632560 53632560 single base substitution G C upstream_gene_variant BRCA-EU X 53632747 53632747 single base substitution G C intron_variant BRCA-EU X 53632747 53632747 single base substitution G C upstream_gene_variant BRCA-EU X 53632798 53632798 single base substitution G C intron_variant BRCA-EU X 53632798 53632798 single base substitution G C upstream_gene_variant BRCA-EU X 53632843 53632843 single base substitution G A intron_variant BRCA-EU X 53632843 53632843 single base substitution G A upstream_gene_variant BRCA-EU X 53632844 53632844 single base substitution A C intron_variant BRCA-EU X 53632844 53632844 single base substitution A C upstream_gene_variant BRCA-EU X 53632912 53632912 single base substitution C T intron_variant BRCA-EU X 53632912 53632912 single base substitution C T upstream_gene_variant BRCA-EU X 53632964 53632964 single base substitution G C intron_variant BRCA-EU X 53632964 53632964 single base substitution G C upstream_gene_variant BRCA-EU X 53633272 53633272 single base substitution G C intron_variant BRCA-EU X 53633272 53633272 single base substitution G C upstream_gene_variant BRCA-EU X 53633626 53633626 single base substitution G T intron_variant BRCA-EU X 53633626 53633626 single base substitution G T upstream_gene_variant BRCA-EU X 53633647 53633647 single base substitution G A intron_variant BRCA-EU X 53633647 53633647 single base substitution G A upstream_gene_variant BRCA-EU X 53633792 53633792 single base substitution G A intron_variant BRCA-EU X 53633792 53633792 single base substitution G A upstream_gene_variant BRCA-EU X 53633793 53633793 single base substitution A G intron_variant BRCA-EU X 53633793 53633793 single base substitution A G upstream_gene_variant BRCA-EU X 53634260 53634260 single base substitution G C intron_variant BRCA-EU X 53634260 53634260 single base substitution G C upstream_gene_variant BRCA-EU X 53635219 53635219 single base substitution G C intron_variant BRCA-EU X 53635219 53635219 single base substitution G C upstream_gene_variant BRCA-EU X 53635281 53635281 single base substitution G A intron_variant BRCA-EU X 53635281 53635281 single base substitution G A upstream_gene_variant BRCA-EU X 53635368 53635368 single base substitution G T intron_variant BRCA-EU X 53635934 53635934 single base substitution G C intron_variant BRCA-EU X 53636339 53636339 single base substitution A G intron_variant BRCA-EU X 53638740 53638740 single base substitution A T downstream_gene_variant BRCA-EU X 53638740 53638740 single base substitution A T intron_variant BRCA-EU X 53639762 53639762 single base substitution G A downstream_gene_variant BRCA-EU X 53639762 53639762 single base substitution G A intron_variant BRCA-EU X 53640688 53640688 single base substitution G A downstream_gene_variant BRCA-EU X 53640688 53640688 single base substitution G A intron_variant BRCA-EU X 53641041 53641041 single base substitution C T downstream_gene_variant BRCA-EU X 53641041 53641041 single base substitution C T intron_variant BRCA-EU X 53642812 53642812 single base substitution G T intron_variant BRCA-EU X 53644410 53644410 deletion of <=200bp A - splice_region_variant BRCA-EU X 53644421 53644421 single base substitution A C intron_variant BRCA-EU X 53645843 53645843 single base substitution A G intron_variant BRCA-EU X 53645844 53645844 single base substitution A G intron_variant BRCA-EU X 53646448 53646448 single base substitution A T intron_variant BRCA-EU X 53648010 53648015 deletion of <=200bp AATCTT - downstream_gene_variant BRCA-EU X 53648010 53648015 deletion of <=200bp AATCTT - intron_variant BRCA-EU X 53648801 53648801 single base substitution C T downstream_gene_variant BRCA-EU X 53648801 53648801 single base substitution C T intron_variant BRCA-EU X 53650294 53650294 single base substitution C A downstream_gene_variant BRCA-EU X 53650294 53650294 single base substitution C A intron_variant BRCA-EU X 53650325 53650325 insertion of <=200bp - A downstream_gene_variant BRCA-EU X 53650325 53650325 insertion of <=200bp - A intron_variant BRCA-EU X 53650700 53650700 single base substitution G C downstream_gene_variant BRCA-EU X 53650700 53650700 single base substitution G C intron_variant BRCA-EU X 53651088 53651088 single base substitution G A downstream_gene_variant BRCA-EU X 53651088 53651088 single base substitution G A intron_variant BRCA-EU X 53651893 53651893 single base substitution A G intron_variant BRCA-EU X 53651914 53651914 deletion of <=200bp A - intron_variant BRCA-EU X 53653749 53653749 single base substitution C T downstream_gene_variant BRCA-EU X 53653749 53653749 single base substitution C T intron_variant BRCA-EU X 53653749 53653749 single base substitution C T upstream_gene_variant BRCA-EU X 53654145 53654145 single base substitution G A downstream_gene_variant BRCA-EU X 53654145 53654145 single base substitution G A intron_variant BRCA-EU X 53654145 53654145 single base substitution G A upstream_gene_variant BRCA-EU X 53654388 53654390 deletion of <=200bp CTT - disruptive_inframe_deletion EG487G BRCA-EU X 53654388 53654390 deletion of <=200bp CTT - disruptive_inframe_deletion EG84G BRCA-EU X 53654388 53654390 deletion of <=200bp CTT - downstream_gene_variant BRCA-EU X 53654388 53654390 deletion of <=200bp CTT - upstream_gene_variant BRCA-EU X 53654518 53654518 single base substitution A T downstream_gene_variant BRCA-EU X 53654518 53654518 single base substitution A T intron_variant BRCA-EU X 53654518 53654518 single base substitution A T upstream_gene_variant BRCA-EU X 53657230 53657230 single base substitution C G downstream_gene_variant BRCA-EU X 53657230 53657230 single base substitution C G intron_variant BRCA-EU X 53657230 53657230 single base substitution C G upstream_gene_variant BRCA-EU X 53658815 53658815 single base substitution C T intron_variant BRCA-EU X 53658815 53658815 single base substitution C T upstream_gene_variant BRCA-EU X 53658832 53658832 insertion of <=200bp - T intron_variant BRCA-EU X 53658832 53658832 insertion of <=200bp - T upstream_gene_variant BRCA-EU X 53658868 53658868 single base substitution T C intron_variant BRCA-EU X 53658868 53658868 single base substitution T C upstream_gene_variant BRCA-EU X 53658922 53658922 single base substitution G C intron_variant BRCA-EU X 53658922 53658922 single base substitution G C upstream_gene_variant BRCA-EU X 53660189 53660189 single base substitution G T intron_variant BRCA-EU X 53660189 53660189 single base substitution G T upstream_gene_variant BRCA-EU X 53661564 53661564 single base substitution G A intron_variant BRCA-EU X 53661564 53661564 single base substitution G A upstream_gene_variant BRCA-EU X 53661717 53661717 single base substitution C T intron_variant BRCA-EU X 53661717 53661717 single base substitution C T upstream_gene_variant BRCA-EU X 53662682 53662682 single base substitution C G intron_variant BRCA-EU X 53662682 53662682 single base substitution C G upstream_gene_variant BRCA-EU X 53662983 53662983 single base substitution C G intron_variant BRCA-EU X 53662983 53662983 single base substitution C G upstream_gene_variant BRCA-EU X 53663970 53663970 single base substitution G C intron_variant BRCA-EU X 53665278 53665278 single base substitution C G intron_variant BRCA-EU X 53665732 53665732 single base substitution C G intron_variant BRCA-EU X 53666005 53666005 single base substitution T A intron_variant BRCA-EU X 53666006 53666006 single base substitution C T intron_variant BRCA-EU X 53668154 53668154 single base substitution T C intron_variant BRCA-EU X 53668275 53668275 single base substitution C A intron_variant BRCA-EU X 53668642 53668642 single base substitution T C intron_variant BRCA-EU X 53669527 53669527 single base substitution G A downstream_gene_variant BRCA-EU X 53669527 53669527 single base substitution G A intron_variant BRCA-EU X 53671826 53671826 single base substitution G A downstream_gene_variant BRCA-EU X 53671826 53671826 single base substitution G A intron_variant BRCA-EU X 53672013 53672013 single base substitution C A downstream_gene_variant BRCA-EU X 53672013 53672013 single base substitution C A intron_variant BRCA-EU X 53673291 53673291 single base substitution G A downstream_gene_variant BRCA-EU X 53673291 53673291 single base substitution G A intron_variant BRCA-EU X 53677445 53677445 single base substitution T A intron_variant BRCA-EU X 53678138 53678138 single base substitution C G intron_variant BRCA-EU X 53678610 53678610 single base substitution C A intron_variant BRCA-EU X 53678844 53678844 single base substitution C G intron_variant BRCA-EU X 53678969 53678969 single base substitution C T intron_variant BRCA-EU X 53679481 53679481 single base substitution T G intron_variant BRCA-EU X 53680923 53680923 single base substitution G T intron_variant BRCA-EU X 53681028 53681028 single base substitution C A synonymous_variant L8L 24G>T BRCA-EU X 53681218 53681218 single base substitution C G intron_variant BRCA-EU X 53681850 53681850 single base substitution G C intron_variant BRCA-EU X 53682225 53682225 single base substitution A T intron_variant BRCA-EU X 53682545 53682545 single base substitution C G intron_variant BRCA-EU X 53682640 53682640 single base substitution C T intron_variant BRCA-EU X 53683350 53683350 single base substitution G T intron_variant BRCA-EU X 53683664 53683664 single base substitution T C intron_variant BRCA-EU X 53684371 53684371 single base substitution G C intron_variant BRCA-EU X 53684942 53684942 single base substitution G A intron_variant BRCA-EU X 53685595 53685595 deletion of <=200bp G - intron_variant BRCA-EU X 53686836 53686836 single base substitution C T intron_variant BRCA-EU X 53688291 53688291 single base substitution C T intron_variant BRCA-EU X 53688801 53688801 single base substitution G T intron_variant BRCA-EU X 53689880 53689880 deletion of <=200bp A - intron_variant BRCA-EU X 53690531 53690531 single base substitution A G intron_variant BRCA-EU X 53693100 53693100 single base substitution C A intron_variant BRCA-EU X 53693319 53693319 single base substitution G C intron_variant BRCA-EU X 53694951 53694951 insertion of <=200bp - T intron_variant BRCA-EU X 53695579 53695579 single base substitution A G intron_variant BRCA-EU X 53696234 53696234 single base substitution G C intron_variant BRCA-EU X 53699014 53699014 single base substitution C A intron_variant BRCA-EU X 53699064 53699064 single base substitution C G intron_variant BRCA-EU X 53699248 53699248 single base substitution C A intron_variant BRCA-EU X 53699286 53699286 single base substitution C G intron_variant BRCA-EU X 53699321 53699321 single base substitution G A intron_variant BRCA-EU X 53700497 53700497 single base substitution G C intron_variant BRCA-EU X 53701613 53701613 single base substitution G T intron_variant BRCA-EU X 53703080 53703080 single base substitution T A intron_variant BRCA-EU X 53704254 53704254 single base substitution C T intron_variant BRCA-EU X 53706591 53706591 deletion of <=200bp A - intron_variant BRCA-EU X 53707355 53707355 single base substitution C A intron_variant BRCA-EU X 53707750 53707750 single base substitution G A intron_variant BRCA-EU X 53708496 53708496 single base substitution C T intron_variant BRCA-EU X 53709427 53709427 single base substitution T C intron_variant BRCA-EU X 53709881 53709881 single base substitution C A intron_variant BRCA-EU X 53710234 53710234 single base substitution G T intron_variant BRCA-EU X 53710289 53710289 single base substitution G A intron_variant BRCA-EU X 53710664 53710664 single base substitution T A intron_variant BRCA-EU X 53710665 53710665 single base substitution C A intron_variant BRCA-EU X 53710916 53710916 single base substitution C T 5_prime_UTR_variant BRCA-EU X 53710916 53710916 single base substitution C T intron_variant BRCA-EU X 53711538 53711538 single base substitution A C intron_variant BRCA-EU X 53711538 53711538 single base substitution A C upstream_gene_variant BRCA-EU X 53712298 53712298 single base substitution C G intron_variant BRCA-EU X 53712298 53712298 single base substitution C G upstream_gene_variant BRCA-EU X 53712643 53712643 single base substitution A G intron_variant BRCA-EU X 53712643 53712643 single base substitution A G upstream_gene_variant BRCA-EU X 53712921 53712921 single base substitution G T intron_variant BRCA-EU X 53712921 53712921 single base substitution G T upstream_gene_variant BRCA-EU X 53713158 53713158 single base substitution G A intron_variant BRCA-EU X 53713158 53713158 single base substitution G A upstream_gene_variant BRCA-EU X 53713443 53713443 deletion of <=200bp C - intron_variant BRCA-EU X 53713443 53713443 deletion of <=200bp C - upstream_gene_variant BRCA-EU X 53713486 53713486 single base substitution G A intron_variant BRCA-EU X 53713486 53713486 single base substitution G A upstream_gene_variant BRCA-EU X 53715298 53715298 insertion of <=200bp - T upstream_gene_variant BRCA-EU X 53715436 53715436 single base substitution G A upstream_gene_variant BRCA-EU X 53715682 53715682 single base substitution C G upstream_gene_variant BRCA-EU X 53715833 53715833 single base substitution C G upstream_gene_variant BRCA-EU X 53715937 53715938 deletion of <=200bp TC - upstream_gene_variant BRCA-EU X 53716181 53716181 single base substitution G T upstream_gene_variant BRCA-EU X 53716369 53716369 single base substitution C T upstream_gene_variant BRCA-EU X 53717223 53717223 insertion of <=200bp - C upstream_gene_variant BRCA-EU X 53717442 53717442 single base substitution G A upstream_gene_variant BRCA-EU X 53717502 53717502 single base substitution G T upstream_gene_variant BRCA-EU X 53717586 53717586 single base substitution C G upstream_gene_variant BRCA-FR X 53559728 53559728 single base substitution G C 3_prime_UTR_variant BRCA-FR X 53559728 53559728 single base substitution G C downstream_gene_variant BRCA-FR X 53561622 53561622 single base substitution C A downstream_gene_variant BRCA-FR X 53561622 53561622 single base substitution C A missense_variant G1051V 3152G>T BRCA-FR X 53561622 53561622 single base substitution C A missense_variant G3262V 9785G>T BRCA-FR X 53561622 53561622 single base substitution C A missense_variant G4229V 12686G>T BRCA-FR X 53561622 53561622 single base substitution C A upstream_gene_variant BRCA-FR X 53566662 53566662 single base substitution C A downstream_gene_variant BRCA-FR X 53566662 53566662 single base substitution C A exon_variant BRCA-FR X 53566662 53566662 single base substitution C A missense_variant C2896F 8687G>T BRCA-FR X 53566662 53566662 single base substitution C A missense_variant C3863F 11588G>T BRCA-FR X 53566662 53566662 single base substitution C A missense_variant C685F 2054G>T BRCA-FR X 53566662 53566662 single base substitution C A upstream_gene_variant BRCA-FR X 53573916 53573916 single base substitution C T intron_variant BRCA-FR X 53573916 53573916 single base substitution C T upstream_gene_variant BRCA-FR X 53577343 53577343 single base substitution C T intron_variant BRCA-FR X 53577343 53577343 single base substitution C T upstream_gene_variant BRCA-FR X 53590423 53590423 single base substitution C T intron_variant BRCA-FR X 53614834 53614834 single base substitution C G intron_variant BRCA-FR X 53615546 53615546 single base substitution T G intron_variant BRCA-FR X 53616165 53616165 single base substitution C A intron_variant BRCA-FR X 53616752 53616752 single base substitution C G missense_variant E1406Q 4216G>C BRCA-FR X 53616752 53616752 single base substitution C G missense_variant E439Q 1315G>C BRCA-FR X 53621762 53621762 single base substitution C G intron_variant BRCA-FR X 53624929 53624929 single base substitution A G intron_variant BRCA-FR X 53627885 53627885 single base substitution C G intron_variant BRCA-FR X 53628215 53628215 single base substitution C T intron_variant BRCA-FR X 53632881 53632881 single base substitution G T intron_variant BRCA-FR X 53632881 53632881 single base substitution G T upstream_gene_variant BRCA-FR X 53633792 53633792 single base substitution G A intron_variant BRCA-FR X 53633792 53633792 single base substitution G A upstream_gene_variant BRCA-FR X 53639762 53639762 single base substitution G A downstream_gene_variant BRCA-FR X 53639762 53639762 single base substitution G A intron_variant BRCA-FR X 53651893 53651893 single base substitution A G intron_variant BRCA-FR X 53655909 53655909 single base substitution C G downstream_gene_variant BRCA-FR X 53655909 53655909 single base substitution C G intron_variant BRCA-FR X 53655909 53655909 single base substitution C G upstream_gene_variant BRCA-FR X 53657230 53657230 single base substitution C G downstream_gene_variant BRCA-FR X 53657230 53657230 single base substitution C G intron_variant BRCA-FR X 53657230 53657230 single base substitution C G upstream_gene_variant BRCA-FR X 53658922 53658922 single base substitution G C intron_variant BRCA-FR X 53658922 53658922 single base substitution G C upstream_gene_variant BRCA-FR X 53662120 53662120 single base substitution A G intron_variant BRCA-FR X 53662120 53662120 single base substitution A G upstream_gene_variant BRCA-FR X 53666005 53666005 single base substitution T A intron_variant BRCA-FR X 53666006 53666006 single base substitution C T intron_variant BRCA-FR X 53672013 53672013 single base substitution C A downstream_gene_variant BRCA-FR X 53672013 53672013 single base substitution C A intron_variant BRCA-FR X 53681218 53681218 single base substitution C G intron_variant BRCA-FR X 53688801 53688801 single base substitution G T intron_variant BRCA-FR X 53695579 53695579 single base substitution A G intron_variant BRCA-FR X 53696234 53696234 single base substitution G C intron_variant BRCA-FR X 53697444 53697444 single base substitution C T intron_variant BRCA-FR X 53701613 53701613 single base substitution G T intron_variant BRCA-FR X 53707355 53707355 single base substitution C A intron_variant BRCA-FR X 53710664 53710664 single base substitution T A intron_variant BRCA-FR X 53710665 53710665 single base substitution C A intron_variant BRCA-FR X 53711532 53711532 single base substitution G A intron_variant BRCA-FR X 53711532 53711532 single base substitution G A upstream_gene_variant BRCA-FR X 53712298 53712298 single base substitution C G intron_variant BRCA-FR X 53712298 53712298 single base substitution C G upstream_gene_variant BRCA-FR X 53717150 53717150 single base substitution C T upstream_gene_variant BRCA-FR X 53717442 53717442 single base substitution G A upstream_gene_variant BRCA-KR X 53566696 53566696 single base substitution T A downstream_gene_variant BRCA-KR X 53566696 53566696 single base substitution T A exon_variant BRCA-KR X 53566696 53566696 single base substitution T A missense_variant S2885C 8653A>T BRCA-KR X 53566696 53566696 single base substitution T A missense_variant S3852C 11554A>T BRCA-KR X 53566696 53566696 single base substitution T A missense_variant S674C 2020A>T BRCA-KR X 53566696 53566696 single base substitution T A upstream_gene_variant BRCA-UK X 53560813 53560813 single base substitution C G downstream_gene_variant BRCA-UK X 53560813 53560813 single base substitution C G exon_variant BRCA-UK X 53560813 53560813 single base substitution C G intron_variant BRCA-UK X 53561008 53561008 single base substitution C G downstream_gene_variant BRCA-UK X 53561008 53561008 single base substitution C G exon_variant BRCA-UK X 53561008 53561008 single base substitution C G missense_variant D1150H 3448G>C BRCA-UK X 53561008 53561008 single base substitution C G missense_variant D3361H 10081G>C BRCA-UK X 53561008 53561008 single base substitution C G missense_variant D4328H 12982G>C BRCA-UK X 53581629 53581629 single base substitution G T missense_variant T1853K 5558C>A BRCA-UK X 53581629 53581629 single base substitution G T missense_variant T2820K 8459C>A BRCA-UK X 53581633 53581633 single base substitution C G missense_variant E1852Q 5554G>C BRCA-UK X 53581633 53581633 single base substitution C G missense_variant E2819Q 8455G>C BRCA-UK X 53587091 53587091 single base substitution A C intron_variant BRCA-UK X 53589773 53589773 single base substitution C G intron_variant BRCA-UK X 53610717 53610717 single base substitution G A downstream_gene_variant BRCA-UK X 53610717 53610717 single base substitution G A missense_variant T1774I 5321C>T BRCA-UK X 53610717 53610717 single base substitution G A missense_variant T807I 2420C>T BRCA-UK X 53611186 53611186 single base substitution G T 3_prime_UTR_variant BRCA-UK X 53611186 53611186 single base substitution G T missense_variant S1707R 5121C>A BRCA-UK X 53611186 53611186 single base substitution G T missense_variant S740R 2220C>A BRCA-UK X 53650700 53650700 single base substitution G C downstream_gene_variant BRCA-UK X 53650700 53650700 single base substitution G C intron_variant BRCA-UK X 53672311 53672311 single base substitution T C downstream_gene_variant BRCA-UK X 53672311 53672311 single base substitution T C synonymous_variant G152G 456A>G BRCA-UK X 53677445 53677445 single base substitution T A intron_variant BRCA-UK X 53686704 53686715 multiple base substitution (>=2bp and <=200bp) GAGATGTTGATA T intron_variant BRCA-UK X 53695988 53695988 single base substitution C G intron_variant BRCA-UK X 53698596 53698596 single base substitution A T intron_variant BRCA-UK X 53698616 53698616 single base substitution A G intron_variant BRCA-UK X 53698635 53698635 single base substitution T A intron_variant BRCA-UK X 53712921 53712921 single base substitution G T intron_variant BRCA-UK X 53712921 53712921 single base substitution G T upstream_gene_variant BRCA-UK X 53714088 53714088 single base substitution C A upstream_gene_variant BRCA-US X 53560294 53560294 single base substitution G A downstream_gene_variant BRCA-US X 53560294 53560294 single base substitution G A synonymous_variant C1189C 3567C>T BRCA-US X 53560294 53560294 single base substitution G A synonymous_variant C3400C 10200C>T BRCA-US X 53560294 53560294 single base substitution G A synonymous_variant C4367C 13101C>T BRCA-US X 53560335 53560335 single base substitution C G downstream_gene_variant BRCA-US X 53560335 53560335 single base substitution C G missense_variant E1176Q 3526G>C BRCA-US X 53560335 53560335 single base substitution C G missense_variant E3387Q 10159G>C BRCA-US X 53560335 53560335 single base substitution C G missense_variant E4354Q 13060G>C BRCA-US X 53561010 53561010 single base substitution C T downstream_gene_variant BRCA-US X 53561010 53561010 single base substitution C T exon_variant BRCA-US X 53561010 53561010 single base substitution C T missense_variant R1149Q 3446G>A BRCA-US X 53561010 53561010 single base substitution C T missense_variant R3360Q 10079G>A BRCA-US X 53561010 53561010 single base substitution C T missense_variant R4327Q 12980G>A BRCA-US X 53561598 53561598 single base substitution C T downstream_gene_variant BRCA-US X 53561598 53561598 single base substitution C T exon_variant BRCA-US X 53561598 53561598 single base substitution C T missense_variant R1059H 3176G>A BRCA-US X 53561598 53561598 single base substitution C T missense_variant R3270H 9809G>A BRCA-US X 53561598 53561598 single base substitution C T missense_variant R4237H 12710G>A BRCA-US X 53561637 53561637 single base substitution G A downstream_gene_variant BRCA-US X 53561637 53561637 single base substitution G A missense_variant A1046V 3137C>T BRCA-US X 53561637 53561637 single base substitution G A missense_variant A3257V 9770C>T BRCA-US X 53561637 53561637 single base substitution G A missense_variant A4224V 12671C>T BRCA-US X 53561637 53561637 single base substitution G A upstream_gene_variant BRCA-US X 53562391 53562391 single base substitution C G downstream_gene_variant BRCA-US X 53562391 53562391 single base substitution C G missense_variant E1023D 3069G>C BRCA-US X 53562391 53562391 single base substitution C G missense_variant E3234D 9702G>C BRCA-US X 53562391 53562391 single base substitution C G missense_variant E4201D 12603G>C BRCA-US X 53562391 53562391 single base substitution C G upstream_gene_variant BRCA-US X 53562452 53562452 single base substitution A C downstream_gene_variant BRCA-US X 53562452 53562452 single base substitution A C missense_variant F1003C 3008T>G BRCA-US X 53562452 53562452 single base substitution A C missense_variant F3214C 9641T>G BRCA-US X 53562452 53562452 single base substitution A C missense_variant F4181C 12542T>G BRCA-US X 53562452 53562452 single base substitution A C upstream_gene_variant BRCA-US X 53563167 53563167 single base substitution C T downstream_gene_variant BRCA-US X 53563167 53563167 single base substitution C T exon_variant BRCA-US X 53563167 53563167 single base substitution C T missense_variant V3191I 9571G>A BRCA-US X 53563167 53563167 single base substitution C T missense_variant V4158I 12472G>A BRCA-US X 53563167 53563167 single base substitution C T missense_variant V980I 2938G>A BRCA-US X 53563167 53563167 single base substitution C T upstream_gene_variant BRCA-US X 53563526 53563526 single base substitution C G downstream_gene_variant BRCA-US X 53563526 53563526 single base substitution C G exon_variant BRCA-US X 53563526 53563526 single base substitution C G missense_variant L3113F 9339G>C BRCA-US X 53563526 53563526 single base substitution C G missense_variant L4080F 12240G>C BRCA-US X 53563526 53563526 single base substitution C G missense_variant L902F 2706G>C BRCA-US X 53563526 53563526 single base substitution C G upstream_gene_variant BRCA-US X 53565354 53565354 single base substitution C A downstream_gene_variant BRCA-US X 53565354 53565354 single base substitution C A exon_variant BRCA-US X 53565354 53565354 single base substitution C A synonymous_variant G3013G 9039G>T BRCA-US X 53565354 53565354 single base substitution C A synonymous_variant G3980G 11940G>T BRCA-US X 53565354 53565354 single base substitution C A synonymous_variant G802G 2406G>T BRCA-US X 53565354 53565354 single base substitution C A upstream_gene_variant BRCA-US X 53566024 53566024 single base substitution C T downstream_gene_variant BRCA-US X 53566024 53566024 single base substitution C T missense_variant E2917K 8749G>A BRCA-US X 53566024 53566024 single base substitution C T missense_variant E3884K 11650G>A BRCA-US X 53566024 53566024 single base substitution C T missense_variant E706K 2116G>A BRCA-US X 53566024 53566024 single base substitution C T upstream_gene_variant BRCA-US X 53570803 53570803 single base substitution G A exon_variant BRCA-US X 53570803 53570803 single base substitution G A intron_variant BRCA-US X 53570803 53570803 single base substitution G A missense_variant T2826M 8477C>T BRCA-US X 53570803 53570803 single base substitution G A missense_variant T3793M 11378C>T BRCA-US X 53570803 53570803 single base substitution G A upstream_gene_variant BRCA-US X 53570824 53570824 single base substitution C T exon_variant BRCA-US X 53570824 53570824 single base substitution C T intron_variant BRCA-US X 53570824 53570824 single base substitution C T missense_variant R2819Q 8456G>A BRCA-US X 53570824 53570824 single base substitution C T missense_variant R3786Q 11357G>A BRCA-US X 53570824 53570824 single base substitution C T upstream_gene_variant BRCA-US X 53573461 53573461 single base substitution G A exon_variant BRCA-US X 53573461 53573461 single base substitution G A synonymous_variant D2650D 7950C>T BRCA-US X 53573461 53573461 single base substitution G A synonymous_variant D3617D 10851C>T BRCA-US X 53573461 53573461 single base substitution G A synonymous_variant D454D 1362C>T BRCA-US X 53573461 53573461 single base substitution G A upstream_gene_variant BRCA-US X 53573667 53573667 single base substitution C G missense_variant E2619Q 7855G>C BRCA-US X 53573667 53573667 single base substitution C G missense_variant E3586Q 10756G>C BRCA-US X 53573667 53573667 single base substitution C G missense_variant E423Q 1267G>C BRCA-US X 53573667 53573667 single base substitution C G splice_region_variant BRCA-US X 53573667 53573667 single base substitution C G upstream_gene_variant BRCA-US X 53574688 53574688 single base substitution C T exon_variant BRCA-US X 53574688 53574688 single base substitution C T missense_variant V2561I 7681G>A BRCA-US X 53574688 53574688 single base substitution C T missense_variant V3528I 10582G>A BRCA-US X 53574688 53574688 single base substitution C T missense_variant V365I 1093G>A BRCA-US X 53574688 53574688 single base substitution C T upstream_gene_variant BRCA-US X 53575140 53575140 single base substitution G C stop_gained S214* 641C>G BRCA-US X 53575140 53575140 single base substitution G C stop_gained S2410* 7229C>G BRCA-US X 53575140 53575140 single base substitution G C stop_gained S3377* 10130C>G BRCA-US X 53575140 53575140 single base substitution G C upstream_gene_variant BRCA-US X 53575991 53575991 single base substitution C T missense_variant V159I 475G>A BRCA-US X 53575991 53575991 single base substitution C T missense_variant V2355I 7063G>A BRCA-US X 53575991 53575991 single base substitution C T missense_variant V3322I 9964G>A BRCA-US X 53575991 53575991 single base substitution C T upstream_gene_variant BRCA-US X 53577889 53577889 single base substitution C T missense_variant A2153T 6457G>A BRCA-US X 53577889 53577889 single base substitution C T missense_variant A3120T 9358G>A BRCA-US X 53577889 53577889 single base substitution C T upstream_gene_variant BRCA-US X 53581746 53581746 single base substitution C T missense_variant G1814E 5441G>A BRCA-US X 53581746 53581746 single base substitution C T missense_variant G2781E 8342G>A BRCA-US X 53587267 53587267 single base substitution T G missense_variant T1573P 4717A>C BRCA-US X 53587267 53587267 single base substitution T G missense_variant T2540P 7618A>C BRCA-US X 53588774 53588774 single base substitution G A missense_variant R1517C 4549C>T BRCA-US X 53588774 53588774 single base substitution G A missense_variant R2484C 7450C>T BRCA-US X 53589093 53589093 single base substitution C T synonymous_variant E1472E 4416G>A BRCA-US X 53589093 53589093 single base substitution C T synonymous_variant E2439E 7317G>A BRCA-US X 53589161 53589161 single base substitution G C missense_variant Q1450E 4348C>G BRCA-US X 53589161 53589161 single base substitution G C missense_variant Q2417E 7249C>G BRCA-US X 53589797 53589797 single base substitution C T missense_variant R1433Q 4298G>A BRCA-US X 53589797 53589797 single base substitution C T missense_variant R2400Q 7199G>A BRCA-US X 53589824 53589824 single base substitution C G missense_variant S1424T 4271G>C BRCA-US X 53589824 53589824 single base substitution C G missense_variant S2391T 7172G>C BRCA-US X 53596651 53596651 single base substitution A C missense_variant V1183G 3548T>G BRCA-US X 53596651 53596651 single base substitution A C missense_variant V2150G 6449T>G BRCA-US X 53602625 53602625 single base substitution G A missense_variant T1036M 3107C>T BRCA-US X 53602625 53602625 single base substitution G A missense_variant T2003M 6008C>T BRCA-US X 53610641 53610641 single base substitution C G downstream_gene_variant BRCA-US X 53610641 53610641 single base substitution C G missense_variant K1799N 5397G>C BRCA-US X 53610641 53610641 single base substitution C G missense_variant K832N 2496G>C BRCA-US X 53610743 53610743 single base substitution C A downstream_gene_variant BRCA-US X 53610743 53610743 single base substitution C A missense_variant M1765I 5295G>T BRCA-US X 53610743 53610743 single base substitution C A missense_variant M798I 2394G>T BRCA-US X 53616683 53616683 single base substitution C T missense_variant D1429N 4285G>A BRCA-US X 53616683 53616683 single base substitution C T missense_variant D462N 1384G>A BRCA-US X 53616739 53616739 single base substitution G T missense_variant A1410D 4229C>A BRCA-US X 53616739 53616739 single base substitution G T missense_variant A443D 1328C>A BRCA-US X 53617397 53617397 single base substitution A T missense_variant D1386E 4158T>A BRCA-US X 53617397 53617397 single base substitution A T missense_variant D419E 1257T>A BRCA-US X 53631552 53631552 single base substitution G C missense_variant Q914E 2740C>G BRCA-US X 53631552 53631552 single base substitution G C upstream_gene_variant BRCA-US X 53631744 53631744 single base substitution A C missense_variant S850A 2548T>G BRCA-US X 53631744 53631744 single base substitution A C upstream_gene_variant BRCA-US X 53642741 53642741 single base substitution G A exon_variant BRCA-US X 53642741 53642741 single base substitution G A synonymous_variant P671P 2013C>T BRCA-US X 53644041 53644041 single base substitution C A exon_variant BRCA-US X 53644041 53644041 single base substitution C A missense_variant R616L 1847G>T BRCA-US X 53644083 53644083 single base substitution C G exon_variant BRCA-US X 53644083 53644083 single base substitution C G missense_variant G602A 1805G>C BRCA-US X 53652126 53652126 single base substitution A G exon_variant BRCA-US X 53652126 53652126 single base substitution A G missense_variant I206T 617T>C BRCA-US X 53652126 53652126 single base substitution A G missense_variant I528T 1583T>C BRCA-US X 53655570 53655570 single base substitution A G downstream_gene_variant BRCA-US X 53655570 53655570 single base substitution A G splice_region_variant BRCA-US X 53655570 53655570 single base substitution A G upstream_gene_variant BRCA-US X 53661226 53661226 single base substitution A T missense_variant F177I 529T>A BRCA-US X 53661226 53661226 single base substitution A T upstream_gene_variant BRCA-US X 53675211 53675211 single base substitution T C missense_variant N30D 88A>G BTCA-JP X 53563261 53563261 single base substitution A T downstream_gene_variant BTCA-JP X 53563261 53563261 single base substitution A T intron_variant BTCA-JP X 53563261 53563261 single base substitution A T upstream_gene_variant BTCA-JP X 53569486 53569486 single base substitution C T downstream_gene_variant BTCA-JP X 53569486 53569486 single base substitution C T exon_variant BTCA-JP X 53569486 53569486 single base substitution C T synonymous_variant Q2831Q 8493G>A BTCA-JP X 53569486 53569486 single base substitution C T synonymous_variant Q3798Q 11394G>A BTCA-JP X 53569486 53569486 single base substitution C T synonymous_variant Q620Q 1860G>A BTCA-JP X 53569486 53569486 single base substitution C T upstream_gene_variant BTCA-JP X 53570870 53570870 single base substitution C T exon_variant BTCA-JP X 53570870 53570870 single base substitution C T missense_variant E2804K 8410G>A BTCA-JP X 53570870 53570870 single base substitution C T missense_variant E3771K 11311G>A BTCA-JP X 53570870 53570870 single base substitution C T missense_variant E608K 1822G>A BTCA-JP X 53570870 53570870 single base substitution C T upstream_gene_variant BTCA-JP X 53576057 53576057 single base substitution T G missense_variant I137L 409A>C BTCA-JP X 53576057 53576057 single base substitution T G missense_variant I2333L 6997A>C BTCA-JP X 53576057 53576057 single base substitution T G missense_variant I3300L 9898A>C BTCA-JP X 53576057 53576057 single base substitution T G upstream_gene_variant BTCA-JP X 53584155 53584155 single base substitution T A intron_variant BTCA-JP X 53585617 53585617 single base substitution T C missense_variant Q1753R 5258A>G BTCA-JP X 53585617 53585617 single base substitution T C missense_variant Q2720R 8159A>G BTCA-JP X 53589990 53589990 deletion of <=200bp T - intron_variant BTCA-JP X 53591593 53591593 single base substitution T C missense_variant E1357G 4070A>G BTCA-JP X 53591593 53591593 single base substitution T C missense_variant E2324G 6971A>G BTCA-JP X 53630307 53630307 insertion of <=200bp - AG intron_variant BTCA-JP X 53630487 53630487 single base substitution C A intron_variant BTCA-JP X 53630487 53630487 single base substitution C A upstream_gene_variant BTCA-JP X 53630517 53630517 deletion of <=200bp A - intron_variant BTCA-JP X 53630517 53630517 deletion of <=200bp A - upstream_gene_variant BTCA-JP X 53644054 53644054 single base substitution A G exon_variant BTCA-JP X 53644054 53644054 single base substitution A G missense_variant C612R 1834T>C BTCA-JP X 53644156 53644156 single base substitution T C intron_variant BTCA-JP X 53654518 53654518 single base substitution A T downstream_gene_variant BTCA-JP X 53654518 53654518 single base substitution A T intron_variant BTCA-JP X 53654518 53654518 single base substitution A T upstream_gene_variant BTCA-JP X 53656390 53656390 single base substitution C A downstream_gene_variant BTCA-JP X 53656390 53656390 single base substitution C A intron_variant BTCA-JP X 53656390 53656390 single base substitution C A upstream_gene_variant BTCA-JP X 53658442 53658442 deletion of <=200bp A - exon_variant BTCA-JP X 53658442 53658442 deletion of <=200bp A - splice_region_variant BTCA-JP X 53658442 53658442 deletion of <=200bp A - upstream_gene_variant BTCA-JP X 53659499 53659499 single base substitution T C synonymous_variant A195A 585A>G BTCA-JP X 53659499 53659499 single base substitution T C upstream_gene_variant CESC-US X 53560326 53560326 single base substitution G A downstream_gene_variant CESC-US X 53560326 53560326 single base substitution G A missense_variant R1179C 3535C>T CESC-US X 53560326 53560326 single base substitution G A missense_variant R3390C 10168C>T CESC-US X 53560326 53560326 single base substitution G A missense_variant R4357C 13069C>T CESC-US X 53564520 53564520 single base substitution C T downstream_gene_variant CESC-US X 53564520 53564520 single base substitution C T exon_variant CESC-US X 53564520 53564520 single base substitution C T missense_variant R3078Q 9233G>A CESC-US X 53564520 53564520 single base substitution C T missense_variant R4045Q 12134G>A CESC-US X 53564520 53564520 single base substitution C T missense_variant R867Q 2600G>A CESC-US X 53564520 53564520 single base substitution C T upstream_gene_variant CESC-US X 53564617 53564617 single base substitution G A downstream_gene_variant CESC-US X 53564617 53564617 single base substitution G A exon_variant CESC-US X 53564617 53564617 single base substitution G A missense_variant R3046W 9136C>T CESC-US X 53564617 53564617 single base substitution G A missense_variant R4013W 12037C>T CESC-US X 53564617 53564617 single base substitution G A missense_variant R835W 2503C>T CESC-US X 53564617 53564617 single base substitution G A upstream_gene_variant CESC-US X 53579331 53579331 single base substitution C T missense_variant R1974Q 5921G>A CESC-US X 53579331 53579331 single base substitution C T missense_variant R2941Q 8822G>A CESC-US X 53579331 53579331 single base substitution C T upstream_gene_variant CESC-US X 53579708 53579708 single base substitution C T missense_variant E1914K 5740G>A CESC-US X 53579708 53579708 single base substitution C T missense_variant E2881K 8641G>A CESC-US X 53579708 53579708 single base substitution C T upstream_gene_variant CESC-US X 53579732 53579732 single base substitution C T missense_variant D1906N 5716G>A CESC-US X 53579732 53579732 single base substitution C T missense_variant D2873N 8617G>A CESC-US X 53579732 53579732 single base substitution C T upstream_gene_variant CESC-US X 53588727 53588727 single base substitution G C missense_variant F1532L 4596C>G CESC-US X 53588727 53588727 single base substitution G C missense_variant F2499L 7497C>G CESC-US X 53589104 53589104 single base substitution C T missense_variant E1469K 4405G>A CESC-US X 53589104 53589104 single base substitution C T missense_variant E2436K 7306G>A CESC-US X 53589158 53589158 single base substitution C A stop_gained E1451* 4351G>T CESC-US X 53589158 53589158 single base substitution C A stop_gained E2418* 7252G>T CESC-US X 53589843 53589843 single base substitution C T missense_variant E1418K 4252G>A CESC-US X 53589843 53589843 single base substitution C T missense_variant E2385K 7153G>A CESC-US X 53591561 53591561 single base substitution C G missense_variant E1368Q 4102G>C CESC-US X 53591561 53591561 single base substitution C G missense_variant E2335Q 7003G>C CESC-US X 53615416 53615416 single base substitution T C missense_variant I1514V 4540A>G CESC-US X 53615416 53615416 single base substitution T C missense_variant I547V 1639A>G CESC-US X 53643957 53643957 single base substitution C T exon_variant CESC-US X 53643957 53643957 single base substitution C T missense_variant R644Q 1931G>A CESC-US X 53644394 53644394 single base substitution C T exon_variant CESC-US X 53644394 53644394 single base substitution C T synonymous_variant V562V 1686G>A CESC-US X 53655822 53655822 single base substitution G C downstream_gene_variant CESC-US X 53655822 53655822 single base substitution G C missense_variant T332R 995C>G CESC-US X 53655822 53655822 single base substitution G C upstream_gene_variant CESC-US X 53672359 53672359 single base substitution A C downstream_gene_variant CESC-US X 53672359 53672359 single base substitution A C missense_variant N136K 408T>G CESC-US X 53675225 53675225 single base substitution T G missense_variant K25T 74A>C CLLE-ES X 53617165 53617165 single base substitution C T intron_variant CLLE-ES X 53628548 53628548 single base substitution A T intron_variant CLLE-ES X 53640418 53640418 single base substitution T G downstream_gene_variant CLLE-ES X 53640418 53640418 single base substitution T G intron_variant CLLE-ES X 53654776 53654776 single base substitution C T downstream_gene_variant CLLE-ES X 53654776 53654776 single base substitution C T missense_variant V30I 88G>A CLLE-ES X 53654776 53654776 single base substitution C T missense_variant V433I 1297G>A CLLE-ES X 53654776 53654776 single base substitution C T upstream_gene_variant CLLE-ES X 53705552 53705552 single base substitution A C intron_variant CLLE-ES X 53717702 53717702 single base substitution T G upstream_gene_variant COAD-US X 53562355 53562355 single base substitution C G downstream_gene_variant COAD-US X 53562355 53562355 single base substitution C G missense_variant M1035I 3105G>C COAD-US X 53562355 53562355 single base substitution C G missense_variant M3246I 9738G>C COAD-US X 53562355 53562355 single base substitution C G missense_variant M4213I 12639G>C COAD-US X 53562355 53562355 single base substitution C G upstream_gene_variant COAD-US X 53564590 53564590 single base substitution G A downstream_gene_variant COAD-US X 53564590 53564590 single base substitution G A exon_variant COAD-US X 53564590 53564590 single base substitution G A missense_variant R3055C 9163C>T COAD-US X 53564590 53564590 single base substitution G A missense_variant R4022C 12064C>T COAD-US X 53564590 53564590 single base substitution G A missense_variant R844C 2530C>T COAD-US X 53564590 53564590 single base substitution G A upstream_gene_variant COAD-US X 53565307 53565307 single base substitution A G downstream_gene_variant COAD-US X 53565307 53565307 single base substitution A G exon_variant COAD-US X 53565307 53565307 single base substitution A G missense_variant V3029A 9086T>C COAD-US X 53565307 53565307 single base substitution A G missense_variant V3996A 11987T>C COAD-US X 53565307 53565307 single base substitution A G missense_variant V818A 2453T>C COAD-US X 53565307 53565307 single base substitution A G upstream_gene_variant COAD-US X 53565948 53565948 single base substitution G A downstream_gene_variant COAD-US X 53565948 53565948 single base substitution G A missense_variant A2942V 8825C>T COAD-US X 53565948 53565948 single base substitution G A missense_variant A3909V 11726C>T COAD-US X 53565948 53565948 single base substitution G A missense_variant A731V 2192C>T COAD-US X 53565948 53565948 single base substitution G A upstream_gene_variant COAD-US X 53571521 53571521 single base substitution C A intron_variant COAD-US X 53571521 53571521 single base substitution C A missense_variant G2784C 8350G>T COAD-US X 53571521 53571521 single base substitution C A missense_variant G3751C 11251G>T COAD-US X 53571521 53571521 single base substitution C A missense_variant G588C 1762G>T COAD-US X 53571521 53571521 single base substitution C A splice_region_variant COAD-US X 53571521 53571521 single base substitution C A upstream_gene_variant COAD-US X 53573497 53573497 single base substitution T C exon_variant COAD-US X 53573497 53573497 single base substitution T C synonymous_variant L2638L 7914A>G COAD-US X 53573497 53573497 single base substitution T C synonymous_variant L3605L 10815A>G COAD-US X 53573497 53573497 single base substitution T C synonymous_variant L442L 1326A>G COAD-US X 53573497 53573497 single base substitution T C upstream_gene_variant COAD-US X 53574943 53574943 single base substitution T C exon_variant COAD-US X 53574943 53574943 single base substitution T C missense_variant I2476V 7426A>G COAD-US X 53574943 53574943 single base substitution T C missense_variant I280V 838A>G COAD-US X 53574943 53574943 single base substitution T C missense_variant I3443V 10327A>G COAD-US X 53574943 53574943 single base substitution T C upstream_gene_variant COAD-US X 53575170 53575170 single base substitution C A missense_variant R204M 611G>T COAD-US X 53575170 53575170 single base substitution C A missense_variant R2400M 7199G>T COAD-US X 53575170 53575170 single base substitution C A missense_variant R3367M 10100G>T COAD-US X 53575170 53575170 single base substitution C A upstream_gene_variant COAD-US X 53577972 53577972 single base substitution T C missense_variant E2125G 6374A>G COAD-US X 53577972 53577972 single base substitution T C missense_variant E3092G 9275A>G COAD-US X 53577972 53577972 single base substitution T C upstream_gene_variant COAD-US X 53587174 53587174 single base substitution G A missense_variant P1604S 4810C>T COAD-US X 53587174 53587174 single base substitution G A missense_variant P2571S 7711C>T COAD-US X 53589090 53589090 single base substitution T C synonymous_variant E1473E 4419A>G COAD-US X 53589090 53589090 single base substitution T C synonymous_variant E2440E 7320A>G COAD-US X 53603879 53603879 single base substitution T C synonymous_variant A1955A 5865A>G COAD-US X 53603879 53603879 single base substitution T C synonymous_variant A988A 2964A>G COAD-US X 53611170 53611170 single base substitution T C downstream_gene_variant COAD-US X 53611170 53611170 single base substitution T C missense_variant K1713E 5137A>G COAD-US X 53611170 53611170 single base substitution T C missense_variant K746E 2236A>G COAD-US X 53613484 53613484 single base substitution G A missense_variant A1597V 4790C>T COAD-US X 53613484 53613484 single base substitution G A missense_variant A630V 1889C>T COAD-US X 53616554 53616554 single base substitution T C missense_variant N1472D 4414A>G COAD-US X 53616554 53616554 single base substitution T C missense_variant N505D 1513A>G COAD-US X 53616678 53616678 single base substitution C T synonymous_variant P1430P 4290G>A COAD-US X 53616678 53616678 single base substitution C T synonymous_variant P463P 1389G>A COAD-US X 53620419 53620419 single base substitution G T missense_variant L1216I 3646C>A COAD-US X 53620419 53620419 single base substitution G T missense_variant L249I 745C>A COAD-US X 53622234 53622234 single base substitution G A missense_variant A1098V 3293C>T COAD-US X 53622234 53622234 single base substitution G A missense_variant A131V 392C>T COAD-US X 53644410 53644410 deletion of <=200bp A - splice_region_variant COAD-US X 53657957 53657957 single base substitution G T exon_variant COAD-US X 53657957 53657957 single base substitution G T synonymous_variant A264A 792C>A COAD-US X 53657957 53657957 single base substitution G T upstream_gene_variant COAD-US X 53658403 53658403 single base substitution G A exon_variant COAD-US X 53658403 53658403 single base substitution G A missense_variant S242F 725C>T COAD-US X 53658403 53658403 single base substitution G A upstream_gene_variant COAD-US X 53672374 53672374 single base substitution C T downstream_gene_variant COAD-US X 53672374 53672374 single base substitution C T synonymous_variant V131V 393G>A COAD-US X 53674479 53674479 single base substitution G A synonymous_variant F61F 183C>T COCA-CN X 53562270 53562270 single base substitution A G downstream_gene_variant COCA-CN X 53562270 53562270 single base substitution A G intron_variant COCA-CN X 53562270 53562270 single base substitution A G upstream_gene_variant COCA-CN X 53572077 53572077 single base substitution C T exon_variant COCA-CN X 53572077 53572077 single base substitution C T missense_variant R2687Q 8060G>A COCA-CN X 53572077 53572077 single base substitution C T missense_variant R3654Q 10961G>A COCA-CN X 53572077 53572077 single base substitution C T missense_variant R491Q 1472G>A COCA-CN X 53572077 53572077 single base substitution C T upstream_gene_variant COCA-CN X 53573477 53573477 single base substitution T C exon_variant COCA-CN X 53573477 53573477 single base substitution T C missense_variant D2645G 7934A>G COCA-CN X 53573477 53573477 single base substitution T C missense_variant D3612G 10835A>G COCA-CN X 53573477 53573477 single base substitution T C missense_variant D449G 1346A>G COCA-CN X 53573477 53573477 single base substitution T C upstream_gene_variant COCA-CN X 53574936 53574936 single base substitution C T exon_variant COCA-CN X 53574936 53574936 single base substitution C T missense_variant R2478Q 7433G>A COCA-CN X 53574936 53574936 single base substitution C T missense_variant R282Q 845G>A COCA-CN X 53574936 53574936 single base substitution C T missense_variant R3445Q 10334G>A COCA-CN X 53574936 53574936 single base substitution C T upstream_gene_variant COCA-CN X 53575239 53575239 single base substitution C T splice_region_variant COCA-CN X 53575239 53575239 single base substitution C T upstream_gene_variant COCA-CN X 53576344 53576344 single base substitution C T missense_variant R2237H 6710G>A COCA-CN X 53576344 53576344 single base substitution C T missense_variant R3204H 9611G>A COCA-CN X 53576344 53576344 single base substitution C T missense_variant R41H 122G>A COCA-CN X 53576344 53576344 single base substitution C T upstream_gene_variant COCA-CN X 53577693 53577693 single base substitution T G missense_variant Q2174P 6521A>C COCA-CN X 53577693 53577693 single base substitution T G missense_variant Q3141P 9422A>C COCA-CN X 53577693 53577693 single base substitution T G upstream_gene_variant COCA-CN X 53578039 53578039 single base substitution G A missense_variant R2103C 6307C>T COCA-CN X 53578039 53578039 single base substitution G A missense_variant R3070C 9208C>T COCA-CN X 53578039 53578039 single base substitution G A upstream_gene_variant COCA-CN X 53578475 53578475 single base substitution G A intron_variant COCA-CN X 53578475 53578475 single base substitution G A upstream_gene_variant COCA-CN X 53579525 53579525 single base substitution A C intron_variant COCA-CN X 53579525 53579525 single base substitution A C upstream_gene_variant COCA-CN X 53584251 53584251 single base substitution T C intron_variant COCA-CN X 53586516 53586516 single base substitution A G intron_variant COCA-CN X 53589216 53589216 single base substitution G T intron_variant COCA-CN X 53595881 53595881 single base substitution C A intron_variant COCA-CN X 53596624 53596624 single base substitution G A missense_variant A1192V 3575C>T COCA-CN X 53596624 53596624 single base substitution G A missense_variant A2159V 6476C>T COCA-CN X 53602555 53602555 single base substitution G A intron_variant COCA-CN X 53607782 53607782 single base substitution G A downstream_gene_variant COCA-CN X 53607782 53607782 single base substitution G A intron_variant COCA-CN X 53611280 53611280 single base substitution C T intron_variant COCA-CN X 53611280 53611280 single base substitution C T missense_variant R1676H 5027G>A COCA-CN X 53611280 53611280 single base substitution C T missense_variant R709H 2126G>A COCA-CN X 53615449 53615449 single base substitution T C missense_variant T1503A 4507A>G COCA-CN X 53615449 53615449 single base substitution T C missense_variant T536A 1606A>G COCA-CN X 53622236 53622236 single base substitution G A synonymous_variant A1097A 3291C>T COCA-CN X 53622236 53622236 single base substitution G A synonymous_variant A130A 390C>T COCA-CN X 53622276 53622276 single base substitution C T missense_variant S1084N 3251G>A COCA-CN X 53622276 53622276 single base substitution C T missense_variant S117N 350G>A COCA-CN X 53629638 53629638 single base substitution T C intron_variant COCA-CN X 53641692 53641692 single base substitution G T downstream_gene_variant COCA-CN X 53641692 53641692 single base substitution G T synonymous_variant I688I 2064C>A COCA-CN X 53652772 53652772 single base substitution G A intron_variant COCA-CN X 53652772 53652772 single base substitution G A synonymous_variant P166P 498C>T COCA-CN X 53652772 53652772 single base substitution G A upstream_gene_variant COCA-CN X 53652787 53652787 single base substitution A G intron_variant COCA-CN X 53652787 53652787 single base substitution A G synonymous_variant G161G 483T>C COCA-CN X 53652787 53652787 single base substitution A G upstream_gene_variant COCA-CN X 53652790 53652790 single base substitution A G intron_variant COCA-CN X 53652790 53652790 single base substitution A G synonymous_variant P160P 480T>C COCA-CN X 53652790 53652790 single base substitution A G upstream_gene_variant COCA-CN X 53652793 53652793 single base substitution A G intron_variant COCA-CN X 53652793 53652793 single base substitution A G synonymous_variant G159G 477T>C COCA-CN X 53652793 53652793 single base substitution A G upstream_gene_variant COCA-CN X 53652808 53652808 single base substitution G A intron_variant COCA-CN X 53652808 53652808 single base substitution G A synonymous_variant P154P 462C>T COCA-CN X 53652808 53652808 single base substitution G A upstream_gene_variant COCA-CN X 53652814 53652814 single base substitution A G intron_variant COCA-CN X 53652814 53652814 single base substitution A G synonymous_variant P152P 456T>C COCA-CN X 53652814 53652814 single base substitution A G upstream_gene_variant COCA-CN X 53652840 53652840 single base substitution G T downstream_gene_variant COCA-CN X 53652840 53652840 single base substitution G T intron_variant COCA-CN X 53652840 53652840 single base substitution G T missense_variant P144T 430C>A COCA-CN X 53652840 53652840 single base substitution G T upstream_gene_variant COCA-CN X 53652846 53652846 single base substitution G T downstream_gene_variant COCA-CN X 53652846 53652846 single base substitution G T intron_variant COCA-CN X 53652846 53652846 single base substitution G T missense_variant P142T 424C>A COCA-CN X 53652846 53652846 single base substitution G T upstream_gene_variant COCA-CN X 53654376 53654376 single base substitution C A downstream_gene_variant COCA-CN X 53654376 53654376 single base substitution C A stop_gained E492* 1474G>T COCA-CN X 53654376 53654376 single base substitution C A stop_gained E89* 265G>T COCA-CN X 53654376 53654376 single base substitution C A upstream_gene_variant COCA-CN X 53654520 53654520 single base substitution T A downstream_gene_variant COCA-CN X 53654520 53654520 single base substitution T A intron_variant COCA-CN X 53654520 53654520 single base substitution T A upstream_gene_variant COCA-CN X 53655746 53655746 single base substitution T C downstream_gene_variant COCA-CN X 53655746 53655746 single base substitution T C synonymous_variant G357G 1071A>G COCA-CN X 53655746 53655746 single base substitution T C upstream_gene_variant COCA-CN X 53656390 53656390 single base substitution C A downstream_gene_variant COCA-CN X 53656390 53656390 single base substitution C A intron_variant COCA-CN X 53656390 53656390 single base substitution C A upstream_gene_variant EOPC-DE X 53570311 53570311 single base substitution T A downstream_gene_variant EOPC-DE X 53570311 53570311 single base substitution T A intron_variant EOPC-DE X 53570311 53570311 single base substitution T A upstream_gene_variant EOPC-DE X 53574779 53574779 single base substitution G A exon_variant EOPC-DE X 53574779 53574779 single base substitution G A synonymous_variant A2530A 7590C>T EOPC-DE X 53574779 53574779 single base substitution G A synonymous_variant A334A 1002C>T EOPC-DE X 53574779 53574779 single base substitution G A synonymous_variant A3497A 10491C>T EOPC-DE X 53574779 53574779 single base substitution G A upstream_gene_variant EOPC-DE X 53587628 53587628 single base substitution G C intron_variant ESCA-CN X 53560061 53560061 single base substitution G A 3_prime_UTR_variant ESCA-CN X 53560061 53560061 single base substitution G A downstream_gene_variant ESCA-CN X 53563194 53563194 single base substitution C T downstream_gene_variant ESCA-CN X 53563194 53563194 single base substitution C T exon_variant ESCA-CN X 53563194 53563194 single base substitution C T missense_variant E3182K 9544G>A ESCA-CN X 53563194 53563194 single base substitution C T missense_variant E4149K 12445G>A ESCA-CN X 53563194 53563194 single base substitution C T missense_variant E971K 2911G>A ESCA-CN X 53563194 53563194 single base substitution C T upstream_gene_variant ESCA-CN X 53563542 53563542 single base substitution T C downstream_gene_variant ESCA-CN X 53563542 53563542 single base substitution T C exon_variant ESCA-CN X 53563542 53563542 single base substitution T C missense_variant N3108S 9323A>G ESCA-CN X 53563542 53563542 single base substitution T C missense_variant N4075S 12224A>G ESCA-CN X 53563542 53563542 single base substitution T C missense_variant N897S 2690A>G ESCA-CN X 53563542 53563542 single base substitution T C upstream_gene_variant ESCA-CN X 53573441 53573441 single base substitution A G exon_variant ESCA-CN X 53573441 53573441 single base substitution A G missense_variant L2657P 7970T>C ESCA-CN X 53573441 53573441 single base substitution A G missense_variant L3624P 10871T>C ESCA-CN X 53573441 53573441 single base substitution A G missense_variant L461P 1382T>C ESCA-CN X 53573441 53573441 single base substitution A G upstream_gene_variant ESCA-CN X 53573758 53573758 single base substitution A C exon_variant ESCA-CN X 53573758 53573758 single base substitution A C synonymous_variant S2588S 7764T>G ESCA-CN X 53573758 53573758 single base substitution A C synonymous_variant S3555S 10665T>G ESCA-CN X 53573758 53573758 single base substitution A C synonymous_variant S392S 1176T>G ESCA-CN X 53573758 53573758 single base substitution A C upstream_gene_variant ESCA-CN X 53584420 53584420 single base substitution C T intron_variant ESCA-CN X 53587276 53587276 single base substitution T C missense_variant T1570A 4708A>G ESCA-CN X 53587276 53587276 single base substitution T C missense_variant T2537A 7609A>G ESCA-CN X 53611997 53611997 single base substitution G A missense_variant T1659M 4976C>T ESCA-CN X 53611997 53611997 single base substitution G A missense_variant T692M 2075C>T ESCA-CN X 53612105 53612105 single base substitution C A missense_variant R1623L 4868G>T ESCA-CN X 53612105 53612105 single base substitution C A missense_variant R656L 1967G>T ESCA-CN X 53620463 53620463 insertion of <=200bp - C frameshift_variant A1201A? ESCA-CN X 53620463 53620463 insertion of <=200bp - C frameshift_variant A234A? ESCA-CN X 53652808 53652808 single base substitution G A intron_variant ESCA-CN X 53652808 53652808 single base substitution G A synonymous_variant P154P 462C>T ESCA-CN X 53652808 53652808 single base substitution G A upstream_gene_variant GBM-US X 53569470 53569470 single base substitution G A downstream_gene_variant GBM-US X 53569470 53569470 single base substitution G A exon_variant GBM-US X 53569470 53569470 single base substitution G A missense_variant R2837W 8509C>T GBM-US X 53569470 53569470 single base substitution G A missense_variant R3804W 11410C>T GBM-US X 53569470 53569470 single base substitution G A missense_variant R626W 1876C>T GBM-US X 53569470 53569470 single base substitution G A upstream_gene_variant GBM-US X 53571567 53571567 single base substitution G A exon_variant GBM-US X 53571567 53571567 single base substitution G A intron_variant GBM-US X 53571567 53571567 single base substitution G A synonymous_variant D2768D 8304C>T GBM-US X 53571567 53571567 single base substitution G A synonymous_variant D3735D 11205C>T GBM-US X 53571567 53571567 single base substitution G A synonymous_variant D572D 1716C>T GBM-US X 53571567 53571567 single base substitution G A upstream_gene_variant GBM-US X 53573431 53573431 single base substitution G A exon_variant GBM-US X 53573431 53573431 single base substitution G A synonymous_variant A2660A 7980C>T GBM-US X 53573431 53573431 single base substitution G A synonymous_variant A3627A 10881C>T GBM-US X 53573431 53573431 single base substitution G A synonymous_variant A464A 1392C>T GBM-US X 53573431 53573431 single base substitution G A upstream_gene_variant GBM-US X 53576344 53576344 single base substitution C T missense_variant R2237H 6710G>A GBM-US X 53576344 53576344 single base substitution C T missense_variant R3204H 9611G>A GBM-US X 53576344 53576344 single base substitution C T missense_variant R41H 122G>A GBM-US X 53576344 53576344 single base substitution C T upstream_gene_variant GBM-US X 53590731 53590731 single base substitution C T missense_variant G1394R 4180G>A GBM-US X 53590731 53590731 single base substitution C T missense_variant G2361R 7081G>A GBM-US X 53600812 53600812 single base substitution A G synonymous_variant T1103T 3309T>C GBM-US X 53600812 53600812 single base substitution A G synonymous_variant T2070T 6210T>C GBM-US X 53612010 53612010 single base substitution G A stop_gained R1655* 4963C>T GBM-US X 53612010 53612010 single base substitution G A stop_gained R688* 2062C>T KIRC-US X 53577912 53577912 single base substitution A T missense_variant L2145Q 6434T>A KIRC-US X 53577912 53577912 single base substitution A T missense_variant L3112Q 9335T>A KIRC-US X 53577912 53577912 single base substitution A T upstream_gene_variant KIRC-US X 53578289 53578289 single base substitution G T missense_variant P2045T 6133C>A KIRC-US X 53578289 53578289 single base substitution G T missense_variant P3012T 9034C>A KIRC-US X 53578289 53578289 single base substitution G T upstream_gene_variant KIRC-US X 53579648 53579648 single base substitution G T missense_variant Q1934K 5800C>A KIRC-US X 53579648 53579648 single base substitution G T missense_variant Q2901K 8701C>A KIRC-US X 53579648 53579648 single base substitution G T upstream_gene_variant KIRC-US X 53579772 53579772 single base substitution T A synonymous_variant T1892T 5676A>T KIRC-US X 53579772 53579772 single base substitution T A synonymous_variant T2859T 8577A>T KIRC-US X 53579772 53579772 single base substitution T A upstream_gene_variant KIRC-US X 53585980 53585980 single base substitution C T missense_variant E1686K 5056G>A KIRC-US X 53585980 53585980 single base substitution C T missense_variant E2653K 7957G>A KIRC-US X 53586385 53586385 single base substitution G T synonymous_variant I1648I 4944C>A KIRC-US X 53586385 53586385 single base substitution G T synonymous_variant I2615I 7845C>A KIRC-US X 53612105 53612105 single base substitution C A missense_variant R1623L 4868G>T KIRC-US X 53612105 53612105 single base substitution C A missense_variant R656L 1967G>T KIRC-US X 53615356 53615356 single base substitution T A missense_variant T1534S 4600A>T KIRC-US X 53615356 53615356 single base substitution T A missense_variant T567S 1699A>T KIRC-US X 53622278 53622278 single base substitution C A missense_variant R1083S 3249G>T KIRC-US X 53622278 53622278 single base substitution C A missense_variant R116S 348G>T KIRC-US X 53674403 53674403 single base substitution C G missense_variant E87Q 259G>C KIRC-US X 53675215 53675215 single base substitution A C synonymous_variant V28V 84T>G KIRP-US X 53564649 53564649 single base substitution C T downstream_gene_variant KIRP-US X 53564649 53564649 single base substitution C T exon_variant KIRP-US X 53564649 53564649 single base substitution C T missense_variant R3035H 9104G>A KIRP-US X 53564649 53564649 single base substitution C T missense_variant R4002H 12005G>A KIRP-US X 53564649 53564649 single base substitution C T missense_variant R824H 2471G>A KIRP-US X 53564649 53564649 single base substitution C T upstream_gene_variant KIRP-US X 53584383 53584383 single base substitution A G synonymous_variant T1755T 5265T>C KIRP-US X 53584383 53584383 single base substitution A G synonymous_variant T2722T 8166T>C KIRP-US X 53589174 53589174 single base substitution C T synonymous_variant E1445E 4335G>A KIRP-US X 53589174 53589174 single base substitution C T synonymous_variant E2412E 7236G>A KIRP-US X 53641559 53641559 single base substitution C T downstream_gene_variant KIRP-US X 53641559 53641559 single base substitution C T missense_variant E733K 2197G>A LAML-CN X 53560325 53560325 single base substitution C T downstream_gene_variant LAML-CN X 53560325 53560325 single base substitution C T missense_variant R1179H 3536G>A LAML-CN X 53560325 53560325 single base substitution C T missense_variant R3390H 10169G>A LAML-CN X 53560325 53560325 single base substitution C T missense_variant R4357H 13070G>A LAML-KR X 53559120 53559120 single base substitution C T 3_prime_UTR_variant LAML-KR X 53559120 53559120 single base substitution C T downstream_gene_variant LAML-KR X 53596493 53596493 single base substitution C A intron_variant LAML-KR X 53652838 53652838 single base substitution G A downstream_gene_variant LAML-KR X 53652838 53652838 single base substitution G A intron_variant LAML-KR X 53652838 53652838 single base substitution G A synonymous_variant P144P 432C>T LAML-KR X 53652838 53652838 single base substitution G A upstream_gene_variant LAML-KR X 53652846 53652846 single base substitution G T downstream_gene_variant LAML-KR X 53652846 53652846 single base substitution G T intron_variant LAML-KR X 53652846 53652846 single base substitution G T missense_variant P142T 424C>A LAML-KR X 53652846 53652846 single base substitution G T upstream_gene_variant LAML-KR X 53652852 53652852 single base substitution T G downstream_gene_variant LAML-KR X 53652852 53652852 single base substitution T G intron_variant LAML-KR X 53652852 53652852 single base substitution T G missense_variant T140P 418A>C LAML-KR X 53652852 53652852 single base substitution T G upstream_gene_variant LAML-KR X 53683002 53683002 single base substitution A G intron_variant LGG-US X 53618082 53618082 single base substitution G C missense_variant L1325V 3973C>G LGG-US X 53618082 53618082 single base substitution G C missense_variant L358V 1072C>G LGG-US X 53654434 53654434 single base substitution C T downstream_gene_variant LGG-US X 53654434 53654434 single base substitution C T synonymous_variant P472P 1416G>A LGG-US X 53654434 53654434 single base substitution C T synonymous_variant P69P 207G>A LGG-US X 53654434 53654434 single base substitution C T upstream_gene_variant LICA-CN X 53565376 53565376 single base substitution G A downstream_gene_variant LICA-CN X 53565376 53565376 single base substitution G A exon_variant LICA-CN X 53565376 53565376 single base substitution G A missense_variant S3006F 9017C>T LICA-CN X 53565376 53565376 single base substitution G A missense_variant S3973F 11918C>T LICA-CN X 53565376 53565376 single base substitution G A missense_variant S795F 2384C>T LICA-CN X 53565376 53565376 single base substitution G A upstream_gene_variant LICA-CN X 53595747 53595747 single base substitution G A synonymous_variant T1237T 3711C>T LICA-CN X 53595747 53595747 single base substitution G A synonymous_variant T2204T 6612C>T LICA-CN X 53611207 53611207 single base substitution T A 3_prime_UTR_variant LICA-CN X 53611207 53611207 single base substitution T A synonymous_variant L1700L 5100A>T LICA-CN X 53611207 53611207 single base substitution T A synonymous_variant L733L 2199A>T LICA-CN X 53620563 53620563 single base substitution T C splice_acceptor_variant LICA-FR X 53559711 53559711 insertion of <=200bp - T 3_prime_UTR_variant LICA-FR X 53559711 53559711 insertion of <=200bp - T downstream_gene_variant LICA-FR X 53561015 53561015 single base substitution G A downstream_gene_variant LICA-FR X 53561015 53561015 single base substitution G A exon_variant LICA-FR X 53561015 53561015 single base substitution G A synonymous_variant I1147I 3441C>T LICA-FR X 53561015 53561015 single base substitution G A synonymous_variant I3358I 10074C>T LICA-FR X 53561015 53561015 single base substitution G A synonymous_variant I4325I 12975C>T LICA-FR X 53571645 53571645 single base substitution A T exon_variant LICA-FR X 53571645 53571645 single base substitution A T intron_variant LICA-FR X 53571645 53571645 single base substitution A T synonymous_variant S2742S 8226T>A LICA-FR X 53571645 53571645 single base substitution A T synonymous_variant S3709S 11127T>A LICA-FR X 53571645 53571645 single base substitution A T synonymous_variant S546S 1638T>A LICA-FR X 53571645 53571645 single base substitution A T upstream_gene_variant LICA-FR X 53572006 53572006 single base substitution C A exon_variant LICA-FR X 53572006 53572006 single base substitution C A missense_variant G2711C 8131G>T LICA-FR X 53572006 53572006 single base substitution C A missense_variant G3678C 11032G>T LICA-FR X 53572006 53572006 single base substitution C A missense_variant G515C 1543G>T LICA-FR X 53572006 53572006 single base substitution C A upstream_gene_variant LICA-FR X 53575159 53575159 single base substitution C T missense_variant A208T 622G>A LICA-FR X 53575159 53575159 single base substitution C T missense_variant A2404T 7210G>A LICA-FR X 53575159 53575159 single base substitution C T missense_variant A3371T 10111G>A LICA-FR X 53575159 53575159 single base substitution C T upstream_gene_variant LICA-FR X 53576299 53576299 single base substitution C A missense_variant R2252L 6755G>T LICA-FR X 53576299 53576299 single base substitution C A missense_variant R3219L 9656G>T LICA-FR X 53576299 53576299 single base substitution C A missense_variant R56L 167G>T LICA-FR X 53576299 53576299 single base substitution C A upstream_gene_variant LICA-FR X 53581856 53581856 single base substitution G C stop_gained Y1777* 5331C>G LICA-FR X 53581856 53581856 single base substitution G C stop_gained Y2744* 8232C>G LICA-FR X 53595827 53595827 single base substitution C A missense_variant A1211S 3631G>T LICA-FR X 53595827 53595827 single base substitution C A missense_variant A2178S 6532G>T LICA-FR X 53595834 53595834 single base substitution C T splice_region_variant LICA-FR X 53604571 53604571 single base substitution C A intron_variant LICA-FR X 53604935 53604935 single base substitution G C intron_variant LICA-FR X 53605156 53605156 single base substitution C T intron_variant LICA-FR X 53622235 53622235 single base substitution C A missense_variant A1098S 3292G>T LICA-FR X 53622235 53622235 single base substitution C A missense_variant A131S 391G>T LICA-FR X 53643936 53643936 insertion of <=200bp - GGAT exon_variant LICA-FR X 53643936 53643936 insertion of <=200bp - GGAT frameshift_variant P651PS? LICA-FR X 53644075 53644075 single base substitution G C exon_variant LICA-FR X 53644075 53644075 single base substitution G C missense_variant P605A 1813C>G LICA-FR X 53646552 53646552 deletion of <=200bp A - intron_variant LICA-FR X 53685270 53685270 single base substitution C T intron_variant LICA-FR X 53688844 53688844 single base substitution T C intron_variant LICA-FR X 53717867 53717867 single base substitution T A upstream_gene_variant LIHC-US X 53563161 53563161 single base substitution G C downstream_gene_variant LIHC-US X 53563161 53563161 single base substitution G C exon_variant LIHC-US X 53563161 53563161 single base substitution G C missense_variant L3193V 9577C>G LIHC-US X 53563161 53563161 single base substitution G C missense_variant L4160V 12478C>G LIHC-US X 53563161 53563161 single base substitution G C missense_variant L982V 2944C>G LIHC-US X 53563161 53563161 single base substitution G C upstream_gene_variant LIHC-US X 53577955 53577955 single base substitution G T synonymous_variant R2131R 6391C>A LIHC-US X 53577955 53577955 single base substitution G T synonymous_variant R3098R 9292C>A LIHC-US X 53577955 53577955 single base substitution G T upstream_gene_variant LIHC-US X 53579842 53579842 single base substitution G T missense_variant P1869Q 5606C>A LIHC-US X 53579842 53579842 single base substitution G T missense_variant P2836Q 8507C>A LIHC-US X 53579842 53579842 single base substitution G T upstream_gene_variant LIHC-US X 53588743 53588743 single base substitution T C missense_variant E1527G 4580A>G LIHC-US X 53588743 53588743 single base substitution T C missense_variant E2494G 7481A>G LIHC-US X 53655712 53655712 single base substitution C T downstream_gene_variant LIHC-US X 53655712 53655712 single base substitution C T missense_variant A369T 1105G>A LIHC-US X 53655712 53655712 single base substitution C T upstream_gene_variant LIHC-US X 53672381 53672381 single base substitution T A downstream_gene_variant LIHC-US X 53672381 53672381 single base substitution T A missense_variant Q129L 386A>T LINC-JP X 53565338 53565338 single base substitution C G downstream_gene_variant LINC-JP X 53565338 53565338 single base substitution C G exon_variant LINC-JP X 53565338 53565338 single base substitution C G missense_variant V3019L 9055G>C LINC-JP X 53565338 53565338 single base substitution C G missense_variant V3986L 11956G>C LINC-JP X 53565338 53565338 single base substitution C G missense_variant V808L 2422G>C LINC-JP X 53565338 53565338 single base substitution C G upstream_gene_variant LINC-JP X 53574498 53574498 single base substitution A C intron_variant LINC-JP X 53574498 53574498 single base substitution A C upstream_gene_variant LINC-JP X 53581083 53581083 single base substitution T C intron_variant LINC-JP X 53581083 53581083 single base substitution T C upstream_gene_variant LINC-JP X 53587582 53587582 single base substitution C A intron_variant LINC-JP X 53589554 53589554 single base substitution T C intron_variant LINC-JP X 53601622 53601622 single base substitution A G intron_variant LINC-JP X 53601731 53601731 single base substitution G A intron_variant LINC-JP X 53614205 53614205 single base substitution T A intron_variant LINC-JP X 53619514 53619514 single base substitution C A synonymous_variant S1272S 3816G>T LINC-JP X 53619514 53619514 single base substitution C A synonymous_variant S305S 915G>T LINC-JP X 53620684 53620684 single base substitution C T intron_variant LINC-JP X 53626144 53626144 single base substitution C A intron_variant LINC-JP X 53635849 53635849 single base substitution A G synonymous_variant R761R 2283T>C LINC-JP X 53636665 53636665 single base substitution T C intron_variant LINC-JP X 53650897 53650905 deletion of <=200bp TTTAGCGTT - downstream_gene_variant LINC-JP X 53650897 53650905 deletion of <=200bp TTTAGCGTT - intron_variant LINC-JP X 53653098 53653098 single base substitution G T downstream_gene_variant LINC-JP X 53653098 53653098 single base substitution G T intron_variant LINC-JP X 53653098 53653098 single base substitution G T upstream_gene_variant LINC-JP X 53653099 53653099 single base substitution A T downstream_gene_variant LINC-JP X 53653099 53653099 single base substitution A T intron_variant LINC-JP X 53653099 53653099 single base substitution A T upstream_gene_variant LINC-JP X 53654763 53654763 single base substitution T C downstream_gene_variant LINC-JP X 53654763 53654763 single base substitution T C missense_variant D34G 101A>G LINC-JP X 53654763 53654763 single base substitution T C missense_variant D437G 1310A>G LINC-JP X 53654763 53654763 single base substitution T C upstream_gene_variant LINC-JP X 53674065 53674065 single base substitution T C downstream_gene_variant LINC-JP X 53674065 53674065 single base substitution T C intron_variant LINC-JP X 53679839 53679839 single base substitution G A intron_variant LINC-JP X 53687071 53687071 single base substitution A T intron_variant LIRI-JP X 53554398 53554398 single base substitution G A downstream_gene_variant LIRI-JP X 53556056 53556056 single base substitution T C downstream_gene_variant LIRI-JP X 53556257 53556257 single base substitution C T downstream_gene_variant LIRI-JP X 53558820 53558820 single base substitution A C downstream_gene_variant LIRI-JP X 53559146 53559146 single base substitution C A 3_prime_UTR_variant LIRI-JP X 53559146 53559146 single base substitution C A downstream_gene_variant LIRI-JP X 53559282 53559282 single base substitution T C 3_prime_UTR_variant LIRI-JP X 53559282 53559282 single base substitution T C downstream_gene_variant LIRI-JP X 53559797 53559797 single base substitution G C 3_prime_UTR_variant LIRI-JP X 53559797 53559797 single base substitution G C downstream_gene_variant LIRI-JP X 53561497 53561497 single base substitution A G downstream_gene_variant LIRI-JP X 53561497 53561497 single base substitution A G exon_variant LIRI-JP X 53561497 53561497 single base substitution A G missense_variant Y1093H 3277T>C LIRI-JP X 53561497 53561497 single base substitution A G missense_variant Y3304H 9910T>C LIRI-JP X 53561497 53561497 single base substitution A G missense_variant Y4271H 12811T>C LIRI-JP X 53564361 53564361 single base substitution A C downstream_gene_variant LIRI-JP X 53564361 53564361 single base substitution A C exon_variant LIRI-JP X 53564361 53564361 single base substitution A C intron_variant LIRI-JP X 53564361 53564361 single base substitution A C upstream_gene_variant LIRI-JP X 53565014 53565014 single base substitution C T downstream_gene_variant LIRI-JP X 53565014 53565014 single base substitution C T intron_variant LIRI-JP X 53565014 53565014 single base substitution C T upstream_gene_variant LIRI-JP X 53565784 53565784 single base substitution A T downstream_gene_variant LIRI-JP X 53565784 53565784 single base substitution A T intron_variant LIRI-JP X 53565784 53565784 single base substitution A T upstream_gene_variant LIRI-JP X 53570819 53570819 single base substitution G A exon_variant LIRI-JP X 53570819 53570819 single base substitution G A intron_variant LIRI-JP X 53570819 53570819 single base substitution G A stop_gained Q2821* 8461C>T LIRI-JP X 53570819 53570819 single base substitution G A stop_gained Q3788* 11362C>T LIRI-JP X 53570819 53570819 single base substitution G A upstream_gene_variant LIRI-JP X 53572220 53572220 single base substitution T C intron_variant LIRI-JP X 53572220 53572220 single base substitution T C upstream_gene_variant LIRI-JP X 53572273 53572273 single base substitution A T intron_variant LIRI-JP X 53572273 53572273 single base substitution A T upstream_gene_variant LIRI-JP X 53573399 53573399 single base substitution A T missense_variant I2671K 8012T>A LIRI-JP X 53573399 53573399 single base substitution A T missense_variant I3638K 10913T>A LIRI-JP X 53573399 53573399 single base substitution A T missense_variant I475K 1424T>A LIRI-JP X 53573399 53573399 single base substitution A T splice_region_variant LIRI-JP X 53573399 53573399 single base substitution A T upstream_gene_variant LIRI-JP X 53573987 53573987 single base substitution C T intron_variant LIRI-JP X 53573987 53573987 single base substitution C T upstream_gene_variant LIRI-JP X 53574808 53574808 single base substitution A T exon_variant LIRI-JP X 53574808 53574808 single base substitution A T missense_variant S2521T 7561T>A LIRI-JP X 53574808 53574808 single base substitution A T missense_variant S325T 973T>A LIRI-JP X 53574808 53574808 single base substitution A T missense_variant S3488T 10462T>A LIRI-JP X 53574808 53574808 single base substitution A T upstream_gene_variant LIRI-JP X 53575059 53575059 single base substitution C G missense_variant G241A 722G>C LIRI-JP X 53575059 53575059 single base substitution C G missense_variant G2437A 7310G>C LIRI-JP X 53575059 53575059 single base substitution C G missense_variant G3404A 10211G>C LIRI-JP X 53575059 53575059 single base substitution C G upstream_gene_variant LIRI-JP X 53575483 53575483 single base substitution G A intron_variant LIRI-JP X 53575483 53575483 single base substitution G A upstream_gene_variant LIRI-JP X 53578436 53578436 single base substitution T A missense_variant S1996C 5986A>T LIRI-JP X 53578436 53578436 single base substitution T A missense_variant S2963C 8887A>T LIRI-JP X 53578436 53578436 single base substitution T A upstream_gene_variant LIRI-JP X 53578527 53578527 single base substitution T C intron_variant LIRI-JP X 53578527 53578527 single base substitution T C upstream_gene_variant LIRI-JP X 53580652 53580652 single base substitution T C intron_variant LIRI-JP X 53580652 53580652 single base substitution T C upstream_gene_variant LIRI-JP X 53581002 53581002 single base substitution G A intron_variant LIRI-JP X 53581002 53581002 single base substitution G A upstream_gene_variant LIRI-JP X 53581180 53581180 single base substitution T A intron_variant LIRI-JP X 53581180 53581180 single base substitution T A upstream_gene_variant LIRI-JP X 53583440 53583440 single base substitution T C intron_variant LIRI-JP X 53584146 53584146 single base substitution G A intron_variant LIRI-JP X 53585978 53585978 single base substitution T G missense_variant E1686D 5058A>C LIRI-JP X 53585978 53585978 single base substitution T G missense_variant E2653D 7959A>C LIRI-JP X 53586802 53586802 single base substitution T C intron_variant LIRI-JP X 53587622 53587622 single base substitution G A intron_variant LIRI-JP X 53588213 53588213 single base substitution C T intron_variant LIRI-JP X 53588547 53588547 single base substitution T C intron_variant LIRI-JP X 53588720 53588720 single base substitution C T missense_variant A1535T 4603G>A LIRI-JP X 53588720 53588720 single base substitution C T missense_variant A2502T 7504G>A LIRI-JP X 53589091 53589093 deletion of <=200bp TCC - disruptive_inframe_deletion EE1472E LIRI-JP X 53589091 53589093 deletion of <=200bp TCC - disruptive_inframe_deletion EE2439E LIRI-JP X 53593376 53593376 single base substitution G A intron_variant LIRI-JP X 53594054 53594054 single base substitution G C intron_variant LIRI-JP X 53594969 53594969 single base substitution G T intron_variant LIRI-JP X 53595730 53595730 single base substitution T C missense_variant N1243S 3728A>G LIRI-JP X 53595730 53595730 single base substitution T C missense_variant N2210S 6629A>G LIRI-JP X 53595803 53595803 single base substitution T C missense_variant I1219V 3655A>G LIRI-JP X 53595803 53595803 single base substitution T C missense_variant I2186V 6556A>G LIRI-JP X 53599521 53599521 single base substitution T A intron_variant LIRI-JP X 53599839 53599839 single base substitution T C intron_variant LIRI-JP X 53600132 53600132 single base substitution G C intron_variant LIRI-JP X 53601375 53601375 single base substitution A T intron_variant LIRI-JP X 53601531 53601531 single base substitution T C intron_variant LIRI-JP X 53602483 53602483 single base substitution A G intron_variant LIRI-JP X 53608513 53608513 single base substitution T C downstream_gene_variant LIRI-JP X 53608513 53608513 single base substitution T C intron_variant LIRI-JP X 53610163 53610163 single base substitution G T downstream_gene_variant LIRI-JP X 53610163 53610163 single base substitution G T intron_variant LIRI-JP X 53610243 53610243 single base substitution G C downstream_gene_variant LIRI-JP X 53610243 53610243 single base substitution G C intron_variant LIRI-JP X 53611480 53611480 single base substitution T C intron_variant LIRI-JP X 53613503 53613503 single base substitution C A missense_variant D1591Y 4771G>T LIRI-JP X 53613503 53613503 single base substitution C A missense_variant D624Y 1870G>T LIRI-JP X 53613637 53613637 single base substitution G A intron_variant LIRI-JP X 53613638 53613638 single base substitution A T intron_variant LIRI-JP X 53614859 53614859 single base substitution T A intron_variant LIRI-JP X 53616829 53616829 single base substitution A C intron_variant LIRI-JP X 53617037 53617037 single base substitution C T intron_variant LIRI-JP X 53617322 53617322 single base substitution T C intron_variant LIRI-JP X 53621327 53621327 single base substitution G C intron_variant LIRI-JP X 53622347 53622347 single base substitution G A synonymous_variant G1060G 3180C>T LIRI-JP X 53622347 53622347 single base substitution G A synonymous_variant G93G 279C>T LIRI-JP X 53634338 53634338 single base substitution A T intron_variant LIRI-JP X 53634338 53634338 single base substitution A T upstream_gene_variant LIRI-JP X 53635096 53635096 single base substitution T C intron_variant LIRI-JP X 53635096 53635096 single base substitution T C upstream_gene_variant LIRI-JP X 53638030 53638030 single base substitution C A downstream_gene_variant LIRI-JP X 53638030 53638030 single base substitution C A intron_variant LIRI-JP X 53642498 53642498 single base substitution T G downstream_gene_variant LIRI-JP X 53642498 53642498 single base substitution T G intron_variant LIRI-JP X 53645073 53645073 single base substitution G A intron_variant LIRI-JP X 53647632 53647632 single base substitution T C downstream_gene_variant LIRI-JP X 53647632 53647632 single base substitution T C intron_variant LIRI-JP X 53649330 53649330 single base substitution A G downstream_gene_variant LIRI-JP X 53649330 53649330 single base substitution A G intron_variant LIRI-JP X 53649964 53649964 single base substitution T C downstream_gene_variant LIRI-JP X 53649964 53649964 single base substitution T C intron_variant LIRI-JP X 53650637 53650637 single base substitution A C downstream_gene_variant LIRI-JP X 53650637 53650637 single base substitution A C intron_variant LIRI-JP X 53652182 53652182 single base substitution T C exon_variant LIRI-JP X 53652182 53652182 single base substitution T C synonymous_variant K187K 561A>G LIRI-JP X 53652182 53652182 single base substitution T C synonymous_variant K509K 1527A>G LIRI-JP X 53653430 53653430 single base substitution T C downstream_gene_variant LIRI-JP X 53653430 53653430 single base substitution T C intron_variant LIRI-JP X 53653430 53653430 single base substitution T C upstream_gene_variant LIRI-JP X 53657718 53657718 single base substitution G C downstream_gene_variant LIRI-JP X 53657718 53657718 single base substitution G C intron_variant LIRI-JP X 53657718 53657718 single base substitution G C upstream_gene_variant LIRI-JP X 53660458 53660458 single base substitution A C intron_variant LIRI-JP X 53660458 53660458 single base substitution A C upstream_gene_variant LIRI-JP X 53660845 53660845 single base substitution T C intron_variant LIRI-JP X 53660845 53660845 single base substitution T C upstream_gene_variant LIRI-JP X 53663090 53663090 single base substitution T C intron_variant LIRI-JP X 53663090 53663090 single base substitution T C upstream_gene_variant LIRI-JP X 53664211 53664211 single base substitution C A intron_variant LIRI-JP X 53664849 53664849 single base substitution T C intron_variant LIRI-JP X 53665517 53665517 single base substitution T C intron_variant LIRI-JP X 53666885 53666885 single base substitution T C intron_variant LIRI-JP X 53668846 53668846 single base substitution C G intron_variant LIRI-JP X 53675464 53675464 single base substitution C T intron_variant LIRI-JP X 53676018 53676018 single base substitution T C intron_variant LIRI-JP X 53676073 53676073 single base substitution G A intron_variant LIRI-JP X 53677193 53677193 single base substitution C T intron_variant LIRI-JP X 53677733 53677733 single base substitution A G intron_variant LIRI-JP X 53678667 53678667 single base substitution T C intron_variant LIRI-JP X 53679110 53679110 single base substitution T C intron_variant LIRI-JP X 53679918 53679918 single base substitution C T intron_variant LIRI-JP X 53680552 53680552 single base substitution T C intron_variant LIRI-JP X 53681653 53681653 single base substitution C T intron_variant LIRI-JP X 53681661 53681661 single base substitution T C intron_variant LIRI-JP X 53683590 53683590 single base substitution T C intron_variant LIRI-JP X 53683753 53683753 single base substitution T C intron_variant LIRI-JP X 53684352 53684352 single base substitution C T intron_variant LIRI-JP X 53687228 53687228 single base substitution T A intron_variant LIRI-JP X 53688631 53688631 single base substitution C T intron_variant LIRI-JP X 53689593 53689593 single base substitution G A intron_variant LIRI-JP X 53690925 53690925 single base substitution T C intron_variant LIRI-JP X 53691630 53691630 single base substitution T C intron_variant LIRI-JP X 53694445 53694445 single base substitution A G intron_variant LIRI-JP X 53695482 53695482 single base substitution G A intron_variant LIRI-JP X 53696030 53696030 single base substitution G T intron_variant LIRI-JP X 53697407 53697407 single base substitution A G intron_variant LIRI-JP X 53699761 53699761 single base substitution G T intron_variant LIRI-JP X 53700115 53700115 single base substitution A T intron_variant LIRI-JP X 53700357 53700357 single base substitution T A intron_variant LIRI-JP X 53704684 53704684 single base substitution A G intron_variant LIRI-JP X 53704830 53704830 single base substitution T C intron_variant LIRI-JP X 53710584 53710584 single base substitution C T intron_variant LIRI-JP X 53713902 53713902 single base substitution T A upstream_gene_variant LIRI-JP X 53716654 53716654 single base substitution A G upstream_gene_variant LIRI-JP X 53718391 53718391 single base substitution G A upstream_gene_variant LUSC-KR X 53560025 53560025 single base substitution C T 3_prime_UTR_variant LUSC-KR X 53560025 53560025 single base substitution C T downstream_gene_variant LUSC-KR X 53563840 53563840 single base substitution A C downstream_gene_variant LUSC-KR X 53563840 53563840 single base substitution A C intron_variant LUSC-KR X 53563840 53563840 single base substitution A C upstream_gene_variant LUSC-KR X 53575016 53575016 single base substitution C T synonymous_variant E2451E 7353G>A LUSC-KR X 53575016 53575016 single base substitution C T synonymous_variant E255E 765G>A LUSC-KR X 53575016 53575016 single base substitution C T synonymous_variant E3418E 10254G>A LUSC-KR X 53575016 53575016 single base substitution C T upstream_gene_variant LUSC-KR X 53577492 53577492 single base substitution C A intron_variant LUSC-KR X 53577492 53577492 single base substitution C A upstream_gene_variant LUSC-KR X 53585434 53585434 single base substitution C A intron_variant LUSC-KR X 53589773 53589773 single base substitution C G intron_variant LUSC-KR X 53604582 53604582 single base substitution G T intron_variant LUSC-KR X 53604716 53604716 single base substitution G A intron_variant LUSC-KR X 53605015 53605015 single base substitution G T intron_variant LUSC-KR X 53605302 53605302 single base substitution T C intron_variant LUSC-KR X 53606015 53606015 single base substitution C T intron_variant LUSC-KR X 53621306 53621306 single base substitution T C intron_variant LUSC-KR X 53634697 53634697 single base substitution G A intron_variant LUSC-KR X 53634697 53634697 single base substitution G A upstream_gene_variant LUSC-KR X 53651424 53651424 single base substitution T C downstream_gene_variant LUSC-KR X 53651424 53651424 single base substitution T C intron_variant LUSC-KR X 53663468 53663468 single base substitution G C intron_variant LUSC-KR X 53663468 53663468 single base substitution G C upstream_gene_variant LUSC-KR X 53664179 53664179 single base substitution C A intron_variant LUSC-KR X 53708395 53708395 single base substitution T A intron_variant LUSC-US X 53563496 53563496 single base substitution G A downstream_gene_variant LUSC-US X 53563496 53563496 single base substitution G A exon_variant LUSC-US X 53563496 53563496 single base substitution G A synonymous_variant T3123T 9369C>T LUSC-US X 53563496 53563496 single base substitution G A synonymous_variant T4090T 12270C>T LUSC-US X 53563496 53563496 single base substitution G A synonymous_variant T912T 2736C>T LUSC-US X 53563496 53563496 single base substitution G A upstream_gene_variant LUSC-US X 53564623 53564623 single base substitution C A downstream_gene_variant LUSC-US X 53564623 53564623 single base substitution C A exon_variant LUSC-US X 53564623 53564623 single base substitution C A missense_variant G3044W 9130G>T LUSC-US X 53564623 53564623 single base substitution C A missense_variant G4011W 12031G>T LUSC-US X 53564623 53564623 single base substitution C A missense_variant G833W 2497G>T LUSC-US X 53564623 53564623 single base substitution C A upstream_gene_variant LUSC-US X 53573708 53573708 single base substitution A T exon_variant LUSC-US X 53573708 53573708 single base substitution A T missense_variant V2605E 7814T>A LUSC-US X 53573708 53573708 single base substitution A T missense_variant V3572E 10715T>A LUSC-US X 53573708 53573708 single base substitution A T missense_variant V409E 1226T>A LUSC-US X 53573708 53573708 single base substitution A T upstream_gene_variant LUSC-US X 53574675 53574675 single base substitution G T exon_variant LUSC-US X 53574675 53574675 single base substitution G T missense_variant T2565N 7694C>A LUSC-US X 53574675 53574675 single base substitution G T missense_variant T3532N 10595C>A LUSC-US X 53574675 53574675 single base substitution G T missense_variant T369N 1106C>A LUSC-US X 53574675 53574675 single base substitution G T upstream_gene_variant LUSC-US X 53574688 53574688 single base substitution C A exon_variant LUSC-US X 53574688 53574688 single base substitution C A missense_variant V2561L 7681G>T LUSC-US X 53574688 53574688 single base substitution C A missense_variant V3528L 10582G>T LUSC-US X 53574688 53574688 single base substitution C A missense_variant V365L 1093G>T LUSC-US X 53574688 53574688 single base substitution C A upstream_gene_variant LUSC-US X 53574689 53574689 single base substitution G A exon_variant LUSC-US X 53574689 53574689 single base substitution G A synonymous_variant V2560V 7680C>T LUSC-US X 53574689 53574689 single base substitution G A synonymous_variant V3527V 10581C>T LUSC-US X 53574689 53574689 single base substitution G A synonymous_variant V364V 1092C>T LUSC-US X 53574689 53574689 single base substitution G A upstream_gene_variant LUSC-US X 53574823 53574823 single base substitution T C exon_variant LUSC-US X 53574823 53574823 single base substitution T C missense_variant T2516A 7546A>G LUSC-US X 53574823 53574823 single base substitution T C missense_variant T320A 958A>G LUSC-US X 53574823 53574823 single base substitution T C missense_variant T3483A 10447A>G LUSC-US X 53574823 53574823 single base substitution T C upstream_gene_variant LUSC-US X 53578044 53578044 single base substitution T C missense_variant D2101G 6302A>G LUSC-US X 53578044 53578044 single base substitution T C missense_variant D3068G 9203A>G LUSC-US X 53578044 53578044 single base substitution T C upstream_gene_variant LUSC-US X 53578078 53578078 single base substitution C A missense_variant D2090Y 6268G>T LUSC-US X 53578078 53578078 single base substitution C A missense_variant D3057Y 9169G>T LUSC-US X 53578078 53578078 single base substitution C A upstream_gene_variant LUSC-US X 53581603 53581603 single base substitution G C missense_variant P1862A 5584C>G LUSC-US X 53581603 53581603 single base substitution G C missense_variant P2829A 8485C>G LUSC-US X 53584372 53584372 single base substitution G C stop_gained S1759* 5276C>G LUSC-US X 53584372 53584372 single base substitution G C stop_gained S2726* 8177C>G LUSC-US X 53587154 53587154 single base substitution C A synonymous_variant L1610L 4830G>T LUSC-US X 53587154 53587154 single base substitution C A synonymous_variant L2577L 7731G>T LUSC-US X 53592131 53592131 single base substitution C G missense_variant Q1292H 3876G>C LUSC-US X 53592131 53592131 single base substitution C G missense_variant Q2259H 6777G>C LUSC-US X 53596671 53596671 single base substitution C A synonymous_variant G1176G 3528G>T LUSC-US X 53596671 53596671 single base substitution C A synonymous_variant G2143G 6429G>T LUSC-US X 53610791 53610791 single base substitution G T downstream_gene_variant LUSC-US X 53610791 53610791 single base substitution G T synonymous_variant G1749G 5247C>A LUSC-US X 53610791 53610791 single base substitution G T synonymous_variant G782G 2346C>A LUSC-US X 53611204 53611204 single base substitution C A 3_prime_UTR_variant LUSC-US X 53611204 53611204 single base substitution C A missense_variant E1701D 5103G>T LUSC-US X 53611204 53611204 single base substitution C A missense_variant E734D 2202G>T LUSC-US X 53616585 53616585 single base substitution C A synonymous_variant V1461V 4383G>T LUSC-US X 53616585 53616585 single base substitution C A synonymous_variant V494V 1482G>T LUSC-US X 53634648 53634648 single base substitution C T missense_variant E778K 2332G>A LUSC-US X 53634648 53634648 single base substitution C T upstream_gene_variant LUSC-US X 53641579 53641579 single base substitution G C downstream_gene_variant LUSC-US X 53641579 53641579 single base substitution G C missense_variant S726C 2177C>G LUSC-US X 53642764 53642764 single base substitution C T exon_variant LUSC-US X 53642764 53642764 single base substitution C T missense_variant D664N 1990G>A LUSC-US X 53659447 53659447 single base substitution C T missense_variant E213K 637G>A LUSC-US X 53659447 53659447 single base substitution C T upstream_gene_variant LUSC-US X 53661239 53661239 single base substitution T A synonymous_variant G172G 516A>T LUSC-US X 53661239 53661239 single base substitution T A upstream_gene_variant LUSC-US X 53661240 53661240 single base substitution C A missense_variant G172V 515G>T LUSC-US X 53661240 53661240 single base substitution C A upstream_gene_variant LUSC-US X 53674517 53674517 single base substitution A G missense_variant C49R 145T>C MALY-DE X 53557764 53557764 single base substitution A C downstream_gene_variant MALY-DE X 53557939 53557939 single base substitution T C downstream_gene_variant MALY-DE X 53561133 53561133 single base substitution C T downstream_gene_variant MALY-DE X 53561133 53561133 single base substitution C T exon_variant MALY-DE X 53561133 53561133 single base substitution C T missense_variant R1108H 3323G>A MALY-DE X 53561133 53561133 single base substitution C T missense_variant R3319H 9956G>A MALY-DE X 53561133 53561133 single base substitution C T missense_variant R4286H 12857G>A MALY-DE X 53563785 53563785 single base substitution G A downstream_gene_variant MALY-DE X 53563785 53563785 single base substitution G A intron_variant MALY-DE X 53563785 53563785 single base substitution G A upstream_gene_variant MALY-DE X 53568395 53568395 insertion of <=200bp - A downstream_gene_variant MALY-DE X 53568395 53568395 insertion of <=200bp - A intron_variant MALY-DE X 53568395 53568395 insertion of <=200bp - A upstream_gene_variant MALY-DE X 53572083 53572083 single base substitution T C exon_variant MALY-DE X 53572083 53572083 single base substitution T C missense_variant Q2685R 8054A>G MALY-DE X 53572083 53572083 single base substitution T C missense_variant Q3652R 10955A>G MALY-DE X 53572083 53572083 single base substitution T C missense_variant Q489R 1466A>G MALY-DE X 53572083 53572083 single base substitution T C upstream_gene_variant MALY-DE X 53573806 53573806 single base substitution A T intron_variant MALY-DE X 53573806 53573806 single base substitution A T upstream_gene_variant MALY-DE X 53582664 53582664 single base substitution G A intron_variant MALY-DE X 53582769 53582769 single base substitution A T intron_variant MALY-DE X 53588257 53588257 single base substitution C G intron_variant MALY-DE X 53589265 53589265 single base substitution G A intron_variant MALY-DE X 53592354 53592354 single base substitution A T intron_variant MALY-DE X 53594101 53594101 single base substitution C T intron_variant MALY-DE X 53618130 53618130 single base substitution T A intron_variant MALY-DE X 53618313 53618313 single base substitution C A intron_variant MALY-DE X 53620590 53620590 single base substitution A C intron_variant MALY-DE X 53629137 53629137 single base substitution T A intron_variant MALY-DE X 53631137 53631137 single base substitution A T intron_variant MALY-DE X 53631137 53631137 single base substitution A T upstream_gene_variant MALY-DE X 53631391 53631391 single base substitution A C intron_variant MALY-DE X 53631391 53631391 single base substitution A C upstream_gene_variant MALY-DE X 53637449 53637449 single base substitution A C intron_variant MALY-DE X 53638828 53638828 single base substitution A T downstream_gene_variant MALY-DE X 53638828 53638828 single base substitution A T intron_variant MALY-DE X 53649622 53649622 single base substitution T G downstream_gene_variant MALY-DE X 53649622 53649622 single base substitution T G intron_variant MALY-DE X 53649645 53649645 single base substitution T A downstream_gene_variant MALY-DE X 53649645 53649645 single base substitution T A intron_variant MALY-DE X 53649764 53649764 single base substitution T C downstream_gene_variant MALY-DE X 53649764 53649764 single base substitution T C intron_variant MALY-DE X 53650269 53650269 single base substitution G C downstream_gene_variant MALY-DE X 53650269 53650269 single base substitution G C intron_variant MALY-DE X 53650506 53650506 single base substitution A C downstream_gene_variant MALY-DE X 53650506 53650506 single base substitution A C intron_variant MALY-DE X 53651285 53651285 single base substitution A T downstream_gene_variant MALY-DE X 53651285 53651285 single base substitution A T intron_variant MALY-DE X 53651723 53651723 single base substitution A G intron_variant MALY-DE X 53653786 53653786 single base substitution T G downstream_gene_variant MALY-DE X 53653786 53653786 single base substitution T G intron_variant MALY-DE X 53653786 53653786 single base substitution T G upstream_gene_variant MALY-DE X 53654520 53654520 single base substitution T A downstream_gene_variant MALY-DE X 53654520 53654520 single base substitution T A intron_variant MALY-DE X 53654520 53654520 single base substitution T A upstream_gene_variant MALY-DE X 53656081 53656081 single base substitution A C downstream_gene_variant MALY-DE X 53656081 53656081 single base substitution A C intron_variant MALY-DE X 53656081 53656081 single base substitution A C upstream_gene_variant MALY-DE X 53657363 53657363 single base substitution T A downstream_gene_variant MALY-DE X 53657363 53657363 single base substitution T A intron_variant MALY-DE X 53657363 53657363 single base substitution T A upstream_gene_variant MALY-DE X 53664398 53664398 single base substitution A G intron_variant MALY-DE X 53664412 53664412 single base substitution T C intron_variant MALY-DE X 53664566 53664566 single base substitution A G intron_variant MALY-DE X 53664614 53664614 single base substitution A C intron_variant MALY-DE X 53665006 53665006 single base substitution C T intron_variant MALY-DE X 53668506 53668506 single base substitution A G intron_variant MALY-DE X 53669824 53669824 insertion of <=200bp - T downstream_gene_variant MALY-DE X 53669824 53669824 insertion of <=200bp - T intron_variant MALY-DE X 53671369 53671369 single base substitution C G downstream_gene_variant MALY-DE X 53671369 53671369 single base substitution C G intron_variant MALY-DE X 53679599 53679599 single base substitution G A intron_variant MALY-DE X 53693735 53693735 single base substitution T C intron_variant MALY-DE X 53706599 53706599 single base substitution C A intron_variant MALY-DE X 53711870 53711870 single base substitution C A intron_variant MALY-DE X 53711870 53711870 single base substitution C A upstream_gene_variant MELA-AU X 53554197 53554197 single base substitution G A downstream_gene_variant MELA-AU X 53554228 53554228 single base substitution A T downstream_gene_variant MELA-AU X 53554501 53554501 single base substitution G A downstream_gene_variant MELA-AU X 53554958 53554958 single base substitution G A downstream_gene_variant MELA-AU X 53554986 53554986 single base substitution G A downstream_gene_variant MELA-AU X 53555046 53555046 single base substitution A T downstream_gene_variant MELA-AU X 53555363 53555363 single base substitution C T downstream_gene_variant MELA-AU X 53557131 53557131 single base substitution C T downstream_gene_variant MELA-AU X 53557395 53557395 single base substitution T G downstream_gene_variant MELA-AU X 53557522 53557522 single base substitution C T downstream_gene_variant MELA-AU X 53558032 53558032 single base substitution T A downstream_gene_variant MELA-AU X 53558462 53558462 single base substitution G A downstream_gene_variant MELA-AU X 53558801 53558801 single base substitution C T downstream_gene_variant MELA-AU X 53559218 53559219 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU X 53559218 53559219 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 53559453 53559453 single base substitution G A 3_prime_UTR_variant MELA-AU X 53559453 53559453 single base substitution G A downstream_gene_variant MELA-AU X 53559663 53559663 single base substitution G A 3_prime_UTR_variant MELA-AU X 53559663 53559663 single base substitution G A downstream_gene_variant MELA-AU X 53559794 53559794 single base substitution G A 3_prime_UTR_variant MELA-AU X 53559794 53559794 single base substitution G A downstream_gene_variant MELA-AU X 53560089 53560089 single base substitution G A 3_prime_UTR_variant MELA-AU X 53560089 53560089 single base substitution G A downstream_gene_variant MELA-AU X 53560457 53560457 single base substitution C T downstream_gene_variant MELA-AU X 53560457 53560457 single base substitution C T intron_variant MELA-AU X 53560960 53560960 single base substitution C T downstream_gene_variant MELA-AU X 53560960 53560960 single base substitution C T exon_variant MELA-AU X 53560960 53560960 single base substitution C T splice_region_variant MELA-AU X 53561382 53561382 single base substitution C T downstream_gene_variant MELA-AU X 53561382 53561382 single base substitution C T intron_variant MELA-AU X 53561922 53561922 single base substitution G A downstream_gene_variant MELA-AU X 53561922 53561922 single base substitution G A intron_variant MELA-AU X 53561922 53561922 single base substitution G A upstream_gene_variant MELA-AU X 53562358 53562358 single base substitution C T downstream_gene_variant MELA-AU X 53562358 53562358 single base substitution C T synonymous_variant Q1034Q 3102G>A MELA-AU X 53562358 53562358 single base substitution C T synonymous_variant Q3245Q 9735G>A MELA-AU X 53562358 53562358 single base substitution C T synonymous_variant Q4212Q 12636G>A MELA-AU X 53562358 53562358 single base substitution C T upstream_gene_variant MELA-AU X 53562562 53562562 single base substitution G A downstream_gene_variant MELA-AU X 53562562 53562562 single base substitution G A intron_variant MELA-AU X 53562562 53562562 single base substitution G A upstream_gene_variant MELA-AU X 53562631 53562631 single base substitution G A downstream_gene_variant MELA-AU X 53562631 53562631 single base substitution G A intron_variant MELA-AU X 53562631 53562631 single base substitution G A upstream_gene_variant MELA-AU X 53562727 53562727 single base substitution G A downstream_gene_variant MELA-AU X 53562727 53562727 single base substitution G A intron_variant MELA-AU X 53562727 53562727 single base substitution G A upstream_gene_variant MELA-AU X 53563512 53563512 single base substitution G A downstream_gene_variant MELA-AU X 53563512 53563512 single base substitution G A exon_variant MELA-AU X 53563512 53563512 single base substitution G A missense_variant P3118L 9353C>T MELA-AU X 53563512 53563512 single base substitution G A missense_variant P4085L 12254C>T MELA-AU X 53563512 53563512 single base substitution G A missense_variant P907L 2720C>T MELA-AU X 53563512 53563512 single base substitution G A upstream_gene_variant MELA-AU X 53565681 53565681 single base substitution A T downstream_gene_variant MELA-AU X 53565681 53565681 single base substitution A T intron_variant MELA-AU X 53565681 53565681 single base substitution A T upstream_gene_variant MELA-AU X 53565689 53565689 single base substitution T A downstream_gene_variant MELA-AU X 53565689 53565689 single base substitution T A intron_variant MELA-AU X 53565689 53565689 single base substitution T A upstream_gene_variant MELA-AU X 53565852 53565852 single base substitution G A downstream_gene_variant MELA-AU X 53565852 53565852 single base substitution G A missense_variant S2974F 8921C>T MELA-AU X 53565852 53565852 single base substitution G A missense_variant S3941F 11822C>T MELA-AU X 53565852 53565852 single base substitution G A missense_variant S763F 2288C>T MELA-AU X 53565852 53565852 single base substitution G A upstream_gene_variant MELA-AU X 53566769 53566769 single base substitution G A downstream_gene_variant MELA-AU X 53566769 53566769 single base substitution G A exon_variant MELA-AU X 53566769 53566769 single base substitution G A synonymous_variant S2860S 8580C>T MELA-AU X 53566769 53566769 single base substitution G A synonymous_variant S3827S 11481C>T MELA-AU X 53566769 53566769 single base substitution G A synonymous_variant S649S 1947C>T MELA-AU X 53566769 53566769 single base substitution G A upstream_gene_variant MELA-AU X 53568531 53568531 single base substitution G A downstream_gene_variant MELA-AU X 53568531 53568531 single base substitution G A intron_variant MELA-AU X 53568531 53568531 single base substitution G A upstream_gene_variant MELA-AU X 53569129 53569129 single base substitution G A downstream_gene_variant MELA-AU X 53569129 53569129 single base substitution G A intron_variant MELA-AU X 53569129 53569129 single base substitution G A upstream_gene_variant MELA-AU X 53569577 53569577 single base substitution C T downstream_gene_variant MELA-AU X 53569577 53569577 single base substitution C T exon_variant MELA-AU X 53569577 53569577 single base substitution C T intron_variant MELA-AU X 53569577 53569577 single base substitution C T upstream_gene_variant MELA-AU X 53569707 53569707 single base substitution C T downstream_gene_variant MELA-AU X 53569707 53569707 single base substitution C T exon_variant MELA-AU X 53569707 53569707 single base substitution C T intron_variant MELA-AU X 53569707 53569707 single base substitution C T upstream_gene_variant MELA-AU X 53570721 53570721 single base substitution G A exon_variant MELA-AU X 53570721 53570721 single base substitution G A intron_variant MELA-AU X 53570721 53570721 single base substitution G A upstream_gene_variant MELA-AU X 53570752 53570752 single base substitution G A exon_variant MELA-AU X 53570752 53570752 single base substitution G A intron_variant MELA-AU X 53570752 53570752 single base substitution G A upstream_gene_variant MELA-AU X 53571054 53571055 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 53571054 53571055 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 53571147 53571147 single base substitution G A intron_variant MELA-AU X 53571147 53571147 single base substitution G A upstream_gene_variant MELA-AU X 53571170 53571170 single base substitution G A intron_variant MELA-AU X 53571170 53571170 single base substitution G A upstream_gene_variant MELA-AU X 53571333 53571333 single base substitution G A intron_variant MELA-AU X 53571333 53571333 single base substitution G A upstream_gene_variant MELA-AU X 53571339 53571339 single base substitution C T intron_variant MELA-AU X 53571339 53571339 single base substitution C T upstream_gene_variant MELA-AU X 53573177 53573177 single base substitution G A intron_variant MELA-AU X 53573177 53573177 single base substitution G A upstream_gene_variant MELA-AU X 53574446 53574446 single base substitution G A intron_variant MELA-AU X 53574446 53574446 single base substitution G A upstream_gene_variant MELA-AU X 53574742 53574742 single base substitution G A exon_variant MELA-AU X 53574742 53574742 single base substitution G A missense_variant P2543S 7627C>T MELA-AU X 53574742 53574742 single base substitution G A missense_variant P347S 1039C>T MELA-AU X 53574742 53574742 single base substitution G A missense_variant P3510S 10528C>T MELA-AU X 53574742 53574742 single base substitution G A upstream_gene_variant MELA-AU X 53575690 53575690 single base substitution G A intron_variant MELA-AU X 53575690 53575690 single base substitution G A upstream_gene_variant MELA-AU X 53575897 53575897 single base substitution G A intron_variant MELA-AU X 53575897 53575897 single base substitution G A upstream_gene_variant MELA-AU X 53576272 53576272 single base substitution G A missense_variant S2261F 6782C>T MELA-AU X 53576272 53576272 single base substitution G A missense_variant S3228F 9683C>T MELA-AU X 53576272 53576272 single base substitution G A missense_variant S65F 194C>T MELA-AU X 53576272 53576272 single base substitution G A upstream_gene_variant MELA-AU X 53576408 53576408 single base substitution G A missense_variant H20Y 58C>T MELA-AU X 53576408 53576408 single base substitution G A missense_variant H2216Y 6646C>T MELA-AU X 53576408 53576408 single base substitution G A missense_variant H3183Y 9547C>T MELA-AU X 53576408 53576408 single base substitution G A upstream_gene_variant MELA-AU X 53576491 53576491 single base substitution G A intron_variant MELA-AU X 53576491 53576491 single base substitution G A upstream_gene_variant MELA-AU X 53576788 53576788 single base substitution C A intron_variant MELA-AU X 53576788 53576788 single base substitution C A upstream_gene_variant MELA-AU X 53576793 53576793 single base substitution A G intron_variant MELA-AU X 53576793 53576793 single base substitution A G upstream_gene_variant MELA-AU X 53576975 53576976 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU X 53576975 53576976 multiple base substitution (>=2bp and <=200bp) AG TA upstream_gene_variant MELA-AU X 53577872 53577872 single base substitution G A synonymous_variant L2158L 6474C>T MELA-AU X 53577872 53577872 single base substitution G A synonymous_variant L3125L 9375C>T MELA-AU X 53577872 53577872 single base substitution G A upstream_gene_variant MELA-AU X 53578413 53578413 single base substitution G C synonymous_variant P2003P 6009C>G MELA-AU X 53578413 53578413 single base substitution G C synonymous_variant P2970P 8910C>G MELA-AU X 53578413 53578413 single base substitution G C upstream_gene_variant MELA-AU X 53579004 53579004 single base substitution C T intron_variant MELA-AU X 53579004 53579004 single base substitution C T upstream_gene_variant MELA-AU X 53579114 53579114 single base substitution G A intron_variant MELA-AU X 53579114 53579114 single base substitution G A upstream_gene_variant MELA-AU X 53580237 53580237 single base substitution G T intron_variant MELA-AU X 53580237 53580237 single base substitution G T upstream_gene_variant MELA-AU X 53580412 53580412 single base substitution G A intron_variant MELA-AU X 53580412 53580412 single base substitution G A upstream_gene_variant MELA-AU X 53581214 53581214 single base substitution G A intron_variant MELA-AU X 53581214 53581214 single base substitution G A upstream_gene_variant MELA-AU X 53582322 53582322 single base substitution T A intron_variant MELA-AU X 53583113 53583113 single base substitution C T intron_variant MELA-AU X 53583860 53583860 single base substitution G A intron_variant MELA-AU X 53585096 53585096 single base substitution C T intron_variant MELA-AU X 53585652 53585652 single base substitution G C synonymous_variant G1741G 5223C>G MELA-AU X 53585652 53585652 single base substitution G C synonymous_variant G2708G 8124C>G MELA-AU X 53585658 53585658 single base substitution A T missense_variant D1739E 5217T>A MELA-AU X 53585658 53585658 single base substitution A T missense_variant D2706E 8118T>A MELA-AU X 53586028 53586028 single base substitution G A splice_region_variant MELA-AU X 53586226 53586226 single base substitution C T intron_variant MELA-AU X 53586411 53586411 single base substitution G A synonymous_variant L1640L 4918C>T MELA-AU X 53586411 53586411 single base substitution G A synonymous_variant L2607L 7819C>T MELA-AU X 53587446 53587446 single base substitution C G intron_variant MELA-AU X 53587475 53587475 single base substitution G A intron_variant MELA-AU X 53587676 53587676 single base substitution G A intron_variant MELA-AU X 53588892 53588892 single base substitution G A splice_region_variant MELA-AU X 53588968 53588968 single base substitution G A intron_variant MELA-AU X 53589083 53589083 single base substitution C T missense_variant E1476K 4426G>A MELA-AU X 53589083 53589083 single base substitution C T missense_variant E2443K 7327G>A MELA-AU X 53589276 53589276 single base substitution G A intron_variant MELA-AU X 53590006 53590006 single base substitution G A intron_variant MELA-AU X 53590291 53590291 single base substitution C T intron_variant MELA-AU X 53590514 53590514 single base substitution C A intron_variant MELA-AU X 53590680 53590680 single base substitution G A intron_variant MELA-AU X 53591126 53591126 single base substitution C T intron_variant MELA-AU X 53591207 53591207 single base substitution C T intron_variant MELA-AU X 53592211 53592211 single base substitution G A intron_variant MELA-AU X 53592611 53592611 single base substitution G A intron_variant MELA-AU X 53593016 53593016 single base substitution C T intron_variant MELA-AU X 53593098 53593098 single base substitution A G intron_variant MELA-AU X 53593227 53593227 single base substitution G A intron_variant MELA-AU X 53593396 53593396 single base substitution G A intron_variant MELA-AU X 53593416 53593416 single base substitution G A intron_variant MELA-AU X 53594134 53594134 single base substitution C T intron_variant MELA-AU X 53594171 53594171 single base substitution G A intron_variant MELA-AU X 53595230 53595230 single base substitution C T intron_variant MELA-AU X 53595442 53595442 single base substitution G A intron_variant MELA-AU X 53595711 53595711 single base substitution G A synonymous_variant F1249F 3747C>T MELA-AU X 53595711 53595711 single base substitution G A synonymous_variant F2216F 6648C>T MELA-AU X 53595843 53595843 single base substitution G A intron_variant MELA-AU X 53595972 53595972 single base substitution A G intron_variant MELA-AU X 53596181 53596181 deletion of <=200bp G - intron_variant MELA-AU X 53596482 53596482 single base substitution G A intron_variant MELA-AU X 53598935 53598935 single base substitution G A intron_variant MELA-AU X 53599254 53599254 single base substitution G A intron_variant MELA-AU X 53599420 53599420 single base substitution T C intron_variant MELA-AU X 53599867 53599867 single base substitution C T intron_variant MELA-AU X 53599871 53599871 single base substitution A G intron_variant MELA-AU X 53600253 53600253 single base substitution G A intron_variant MELA-AU X 53600538 53600538 single base substitution G A intron_variant MELA-AU X 53600808 53600808 single base substitution G A missense_variant L1105F 3313C>T MELA-AU X 53600808 53600808 single base substitution G A missense_variant L2072F 6214C>T MELA-AU X 53601559 53601559 single base substitution A G intron_variant MELA-AU X 53602078 53602078 single base substitution G A intron_variant MELA-AU X 53602206 53602206 single base substitution C T intron_variant MELA-AU X 53602753 53602753 single base substitution G A splice_region_variant MELA-AU X 53603514 53603514 single base substitution C T intron_variant MELA-AU X 53604263 53604263 single base substitution G A intron_variant MELA-AU X 53606917 53606917 single base substitution T A downstream_gene_variant MELA-AU X 53606917 53606917 single base substitution T A intron_variant MELA-AU X 53607561 53607561 single base substitution G A downstream_gene_variant MELA-AU X 53607561 53607561 single base substitution G A intron_variant MELA-AU X 53608017 53608017 single base substitution T C downstream_gene_variant MELA-AU X 53608017 53608017 single base substitution T C intron_variant MELA-AU X 53610812 53610812 single base substitution G A downstream_gene_variant MELA-AU X 53610812 53610812 single base substitution G A synonymous_variant I1742I 5226C>T MELA-AU X 53610812 53610812 single base substitution G A synonymous_variant I775I 2325C>T MELA-AU X 53610888 53610888 single base substitution G A downstream_gene_variant MELA-AU X 53610888 53610888 single base substitution G A intron_variant MELA-AU X 53610894 53610894 single base substitution A G downstream_gene_variant MELA-AU X 53610894 53610894 single base substitution A G intron_variant MELA-AU X 53611027 53611027 single base substitution G A downstream_gene_variant MELA-AU X 53611027 53611027 single base substitution G A intron_variant MELA-AU X 53611302 53611302 single base substitution T A intron_variant MELA-AU X 53611302 53611302 single base substitution T A missense_variant N1669Y 5005A>T MELA-AU X 53611302 53611302 single base substitution T A missense_variant N702Y 2104A>T MELA-AU X 53611839 53611839 single base substitution G A intron_variant MELA-AU X 53612640 53612640 single base substitution T C intron_variant MELA-AU X 53612789 53612789 single base substitution G A intron_variant MELA-AU X 53614263 53614264 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 53614328 53614328 single base substitution G A intron_variant MELA-AU X 53614396 53614396 single base substitution G A intron_variant MELA-AU X 53614977 53614977 single base substitution C T intron_variant MELA-AU X 53615803 53615803 single base substitution A G intron_variant MELA-AU X 53615904 53615904 single base substitution C T intron_variant MELA-AU X 53616241 53616241 single base substitution G A intron_variant MELA-AU X 53616291 53616291 single base substitution G T intron_variant MELA-AU X 53616611 53616611 single base substitution C T missense_variant E1453K 4357G>A MELA-AU X 53616611 53616611 single base substitution C T missense_variant E486K 1456G>A MELA-AU X 53617258 53617258 single base substitution C T intron_variant MELA-AU X 53617507 53617507 single base substitution G A intron_variant MELA-AU X 53617573 53617573 single base substitution G A intron_variant MELA-AU X 53617905 53617905 single base substitution G A intron_variant MELA-AU X 53618127 53618160 deletion of <=200bp AAATACATTTTTAAAAGGAAGGAACCTTTTCAAG - intron_variant MELA-AU X 53618197 53618197 single base substitution A C intron_variant MELA-AU X 53618253 53618253 single base substitution T C intron_variant MELA-AU X 53620105 53620105 single base substitution G A intron_variant MELA-AU X 53620256 53620256 single base substitution G A intron_variant MELA-AU X 53620745 53620745 single base substitution C T intron_variant MELA-AU X 53620993 53620993 single base substitution C T intron_variant MELA-AU X 53621973 53621973 single base substitution G A intron_variant MELA-AU X 53622156 53622156 single base substitution G A missense_variant P1124L 3371C>T MELA-AU X 53622156 53622156 single base substitution G A missense_variant P157L 470C>T MELA-AU X 53622919 53622919 single base substitution G A intron_variant MELA-AU X 53623088 53623088 single base substitution C T intron_variant MELA-AU X 53623297 53623297 single base substitution G A intron_variant MELA-AU X 53623876 53623876 single base substitution G A intron_variant MELA-AU X 53624982 53624982 single base substitution A G intron_variant MELA-AU X 53625947 53625947 single base substitution G A intron_variant MELA-AU X 53626319 53626319 single base substitution G A intron_variant MELA-AU X 53627035 53627035 single base substitution G A intron_variant MELA-AU X 53628578 53628578 single base substitution A T intron_variant MELA-AU X 53629127 53629127 single base substitution G A intron_variant MELA-AU X 53629428 53629428 single base substitution G A intron_variant MELA-AU X 53630442 53630442 single base substitution G A synonymous_variant S921S 2763C>T MELA-AU X 53630442 53630442 single base substitution G A upstream_gene_variant MELA-AU X 53630453 53630453 single base substitution G A missense_variant R918C 2752C>T MELA-AU X 53630453 53630453 single base substitution G A upstream_gene_variant MELA-AU X 53631035 53631035 single base substitution C T intron_variant MELA-AU X 53631035 53631035 single base substitution C T upstream_gene_variant MELA-AU X 53631783 53631783 single base substitution C T missense_variant E837K 2509G>A MELA-AU X 53631783 53631783 single base substitution C T upstream_gene_variant MELA-AU X 53632106 53632106 single base substitution C A intron_variant MELA-AU X 53632106 53632106 single base substitution C A upstream_gene_variant MELA-AU X 53632175 53632175 single base substitution C T intron_variant MELA-AU X 53632175 53632175 single base substitution C T upstream_gene_variant MELA-AU X 53632656 53632656 single base substitution G A intron_variant MELA-AU X 53632656 53632656 single base substitution G A upstream_gene_variant MELA-AU X 53632835 53632835 single base substitution G A intron_variant MELA-AU X 53632835 53632835 single base substitution G A upstream_gene_variant MELA-AU X 53633391 53633391 single base substitution G A intron_variant MELA-AU X 53633391 53633391 single base substitution G A upstream_gene_variant MELA-AU X 53634116 53634116 single base substitution G A intron_variant MELA-AU X 53634116 53634116 single base substitution G A upstream_gene_variant MELA-AU X 53634181 53634181 single base substitution G A intron_variant MELA-AU X 53634181 53634181 single base substitution G A upstream_gene_variant MELA-AU X 53635110 53635110 single base substitution G A intron_variant MELA-AU X 53635110 53635110 single base substitution G A upstream_gene_variant MELA-AU X 53635877 53635877 single base substitution G A splice_region_variant MELA-AU X 53635937 53635937 single base substitution G A intron_variant MELA-AU X 53636023 53636023 single base substitution C T intron_variant MELA-AU X 53636439 53636439 single base substitution G A intron_variant MELA-AU X 53636615 53636615 single base substitution T A intron_variant MELA-AU X 53636991 53636991 single base substitution A G intron_variant MELA-AU X 53637550 53637550 single base substitution T C intron_variant MELA-AU X 53638065 53638065 single base substitution T C downstream_gene_variant MELA-AU X 53638065 53638065 single base substitution T C intron_variant MELA-AU X 53638427 53638427 single base substitution A T downstream_gene_variant MELA-AU X 53638427 53638427 single base substitution A T intron_variant MELA-AU X 53638934 53638951 deletion of <=200bp ATGGATATGGAGGAAGGG - downstream_gene_variant MELA-AU X 53638934 53638951 deletion of <=200bp ATGGATATGGAGGAAGGG - intron_variant MELA-AU X 53639120 53639120 single base substitution A G downstream_gene_variant MELA-AU X 53639120 53639120 single base substitution A G intron_variant MELA-AU X 53639161 53639161 single base substitution T A downstream_gene_variant MELA-AU X 53639161 53639161 single base substitution T A intron_variant MELA-AU X 53639521 53639521 single base substitution G A downstream_gene_variant MELA-AU X 53639521 53639521 single base substitution G A intron_variant MELA-AU X 53641090 53641090 single base substitution G A downstream_gene_variant MELA-AU X 53641090 53641090 single base substitution G A intron_variant MELA-AU X 53641341 53641341 single base substitution G A downstream_gene_variant MELA-AU X 53641341 53641341 single base substitution G A intron_variant MELA-AU X 53642190 53642190 single base substitution G A downstream_gene_variant MELA-AU X 53642190 53642190 single base substitution G A intron_variant MELA-AU X 53643038 53643038 single base substitution G A intron_variant MELA-AU X 53643273 53643273 single base substitution G A intron_variant MELA-AU X 53643397 53643397 single base substitution A C intron_variant MELA-AU X 53643954 53643954 single base substitution C T exon_variant MELA-AU X 53643954 53643954 single base substitution C T missense_variant R645K 1934G>A MELA-AU X 53645531 53645531 single base substitution T A intron_variant MELA-AU X 53645992 53645992 single base substitution T C intron_variant MELA-AU X 53646682 53646682 single base substitution G A downstream_gene_variant MELA-AU X 53646682 53646682 single base substitution G A intron_variant MELA-AU X 53647308 53647308 single base substitution C T downstream_gene_variant MELA-AU X 53647308 53647308 single base substitution C T intron_variant MELA-AU X 53647398 53647398 single base substitution C T downstream_gene_variant MELA-AU X 53647398 53647398 single base substitution C T intron_variant MELA-AU X 53647703 53647703 single base substitution C T downstream_gene_variant MELA-AU X 53647703 53647703 single base substitution C T intron_variant MELA-AU X 53648006 53648006 single base substitution G T downstream_gene_variant MELA-AU X 53648006 53648006 single base substitution G T intron_variant MELA-AU X 53648256 53648256 single base substitution G A downstream_gene_variant MELA-AU X 53648256 53648256 single base substitution G A intron_variant MELA-AU X 53649231 53649231 single base substitution C T downstream_gene_variant MELA-AU X 53649231 53649231 single base substitution C T intron_variant MELA-AU X 53651204 53651204 single base substitution C T downstream_gene_variant MELA-AU X 53651204 53651204 single base substitution C T intron_variant MELA-AU X 53651740 53651740 single base substitution A C intron_variant MELA-AU X 53654518 53654518 single base substitution A T downstream_gene_variant MELA-AU X 53654518 53654518 single base substitution A T intron_variant MELA-AU X 53654518 53654518 single base substitution A T upstream_gene_variant MELA-AU X 53654548 53654548 single base substitution G A downstream_gene_variant MELA-AU X 53654548 53654548 single base substitution G A intron_variant MELA-AU X 53654548 53654548 single base substitution G A upstream_gene_variant MELA-AU X 53654729 53654729 single base substitution T C downstream_gene_variant MELA-AU X 53654729 53654729 single base substitution T C synonymous_variant Q448Q 1344A>G MELA-AU X 53654729 53654729 single base substitution T C synonymous_variant Q45Q 135A>G MELA-AU X 53654729 53654729 single base substitution T C upstream_gene_variant MELA-AU X 53656306 53656306 single base substitution G A downstream_gene_variant MELA-AU X 53656306 53656306 single base substitution G A intron_variant MELA-AU X 53656306 53656306 single base substitution G A upstream_gene_variant MELA-AU X 53656804 53656804 single base substitution G A downstream_gene_variant MELA-AU X 53656804 53656804 single base substitution G A intron_variant MELA-AU X 53656804 53656804 single base substitution G A upstream_gene_variant MELA-AU X 53657562 53657562 single base substitution G A downstream_gene_variant MELA-AU X 53657562 53657562 single base substitution G A intron_variant MELA-AU X 53657562 53657562 single base substitution G A upstream_gene_variant MELA-AU X 53657950 53657950 single base substitution A C exon_variant MELA-AU X 53657950 53657950 single base substitution A C missense_variant F267V 799T>G MELA-AU X 53657950 53657950 single base substitution A C upstream_gene_variant MELA-AU X 53659406 53659406 single base substitution G A intron_variant MELA-AU X 53659406 53659406 single base substitution G A upstream_gene_variant MELA-AU X 53661824 53661824 single base substitution G A intron_variant MELA-AU X 53661824 53661824 single base substitution G A upstream_gene_variant MELA-AU X 53661907 53661907 single base substitution T C intron_variant MELA-AU X 53661907 53661907 single base substitution T C upstream_gene_variant MELA-AU X 53662076 53662076 single base substitution G A intron_variant MELA-AU X 53662076 53662076 single base substitution G A upstream_gene_variant MELA-AU X 53662215 53662215 single base substitution A G intron_variant MELA-AU X 53662215 53662215 single base substitution A G upstream_gene_variant MELA-AU X 53662508 53662508 single base substitution G A intron_variant MELA-AU X 53662508 53662508 single base substitution G A upstream_gene_variant MELA-AU X 53663333 53663333 single base substitution G A intron_variant MELA-AU X 53663333 53663333 single base substitution G A upstream_gene_variant MELA-AU X 53664998 53664998 single base substitution G A intron_variant MELA-AU X 53665823 53665823 single base substitution C T intron_variant MELA-AU X 53666121 53666121 single base substitution A G intron_variant MELA-AU X 53667132 53667132 single base substitution G A intron_variant MELA-AU X 53668751 53668752 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 53670574 53670574 single base substitution G A downstream_gene_variant MELA-AU X 53670574 53670574 single base substitution G A intron_variant MELA-AU X 53670626 53670626 single base substitution T C downstream_gene_variant MELA-AU X 53670626 53670626 single base substitution T C intron_variant MELA-AU X 53670839 53670839 single base substitution G A downstream_gene_variant MELA-AU X 53670839 53670839 single base substitution G A intron_variant MELA-AU X 53671034 53671035 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU X 53671034 53671035 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 53671580 53671580 single base substitution A T downstream_gene_variant MELA-AU X 53671580 53671580 single base substitution A T intron_variant MELA-AU X 53671747 53671747 single base substitution G A downstream_gene_variant MELA-AU X 53671747 53671747 single base substitution G A intron_variant MELA-AU X 53672236 53672236 single base substitution C T downstream_gene_variant MELA-AU X 53672236 53672236 single base substitution C T intron_variant MELA-AU X 53672744 53672744 single base substitution A G downstream_gene_variant MELA-AU X 53672744 53672744 single base substitution A G intron_variant MELA-AU X 53673533 53673533 single base substitution A G downstream_gene_variant MELA-AU X 53673533 53673533 single base substitution A G intron_variant MELA-AU X 53673697 53673697 single base substitution G A downstream_gene_variant MELA-AU X 53673697 53673697 single base substitution G A intron_variant MELA-AU X 53675036 53675036 single base substitution G C intron_variant MELA-AU X 53675325 53675325 single base substitution G A intron_variant MELA-AU X 53675830 53675830 single base substitution C T intron_variant MELA-AU X 53675963 53675964 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU X 53676164 53676164 single base substitution C T intron_variant MELA-AU X 53676747 53676747 single base substitution T G intron_variant MELA-AU X 53677104 53677104 single base substitution C T intron_variant MELA-AU X 53677882 53677882 single base substitution G A intron_variant MELA-AU X 53677982 53677982 single base substitution C T intron_variant MELA-AU X 53678510 53678510 single base substitution A G intron_variant MELA-AU X 53678840 53678841 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU X 53679262 53679262 single base substitution A C intron_variant MELA-AU X 53680118 53680118 single base substitution G A intron_variant MELA-AU X 53680265 53680265 single base substitution G A intron_variant MELA-AU X 53680980 53680980 single base substitution A G intron_variant MELA-AU X 53681320 53681320 single base substitution G A intron_variant MELA-AU X 53681769 53681769 single base substitution A G intron_variant MELA-AU X 53682895 53682895 single base substitution C T intron_variant MELA-AU X 53683035 53683035 single base substitution G A intron_variant MELA-AU X 53683444 53683444 single base substitution C T intron_variant MELA-AU X 53684424 53684424 single base substitution C T intron_variant MELA-AU X 53685530 53685530 single base substitution G A intron_variant MELA-AU X 53685979 53685979 single base substitution G A intron_variant MELA-AU X 53686526 53686526 single base substitution G A intron_variant MELA-AU X 53688282 53688282 single base substitution C T intron_variant MELA-AU X 53688355 53688355 single base substitution G A intron_variant MELA-AU X 53689221 53689221 single base substitution C T intron_variant MELA-AU X 53689712 53689712 single base substitution G C intron_variant MELA-AU X 53689836 53689836 single base substitution A G intron_variant MELA-AU X 53689953 53689953 single base substitution G A intron_variant MELA-AU X 53690472 53690472 single base substitution G A intron_variant MELA-AU X 53690692 53690692 single base substitution A C intron_variant MELA-AU X 53690693 53690693 single base substitution G A intron_variant MELA-AU X 53690854 53690854 single base substitution G A intron_variant MELA-AU X 53691232 53691232 single base substitution C T intron_variant MELA-AU X 53691645 53691645 single base substitution C T intron_variant MELA-AU X 53692356 53692356 single base substitution G A intron_variant MELA-AU X 53693179 53693180 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 53693634 53693634 single base substitution C T intron_variant MELA-AU X 53694005 53694005 single base substitution G A intron_variant MELA-AU X 53694022 53694022 single base substitution G A intron_variant MELA-AU X 53694697 53694697 single base substitution G A intron_variant MELA-AU X 53695476 53695476 single base substitution G A intron_variant MELA-AU X 53695624 53695625 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 53696441 53696441 single base substitution A G intron_variant MELA-AU X 53696615 53696615 single base substitution G T intron_variant MELA-AU X 53697744 53697744 single base substitution G A intron_variant MELA-AU X 53698082 53698082 single base substitution G A intron_variant MELA-AU X 53698122 53698122 single base substitution T C intron_variant MELA-AU X 53698585 53698585 single base substitution A T intron_variant MELA-AU X 53698694 53698694 single base substitution G A intron_variant MELA-AU X 53698727 53698727 single base substitution G A intron_variant MELA-AU X 53698873 53698873 single base substitution G A intron_variant MELA-AU X 53699406 53699406 single base substitution G A intron_variant MELA-AU X 53699433 53699433 single base substitution C T intron_variant MELA-AU X 53701392 53701392 single base substitution C T intron_variant MELA-AU X 53701477 53701477 single base substitution G A intron_variant MELA-AU X 53701866 53701866 single base substitution G C intron_variant MELA-AU X 53702049 53702049 single base substitution G A intron_variant MELA-AU X 53702782 53702782 single base substitution G A intron_variant MELA-AU X 53703229 53703229 single base substitution G A intron_variant MELA-AU X 53703490 53703490 single base substitution C T intron_variant MELA-AU X 53703793 53703793 single base substitution G A intron_variant MELA-AU X 53704099 53704099 single base substitution G C intron_variant MELA-AU X 53704166 53704166 single base substitution G A intron_variant MELA-AU X 53704772 53704772 single base substitution G T intron_variant MELA-AU X 53705512 53705512 single base substitution G A intron_variant MELA-AU X 53708156 53708157 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 53708616 53708616 single base substitution G A intron_variant MELA-AU X 53709409 53709409 single base substitution G A intron_variant MELA-AU X 53711344 53711344 single base substitution G A intron_variant MELA-AU X 53711344 53711344 single base substitution G A upstream_gene_variant MELA-AU X 53711345 53711345 single base substitution G A intron_variant MELA-AU X 53711345 53711345 single base substitution G A upstream_gene_variant MELA-AU X 53711449 53711449 single base substitution C T intron_variant MELA-AU X 53711449 53711449 single base substitution C T upstream_gene_variant MELA-AU X 53712526 53712526 single base substitution C T intron_variant MELA-AU X 53712526 53712526 single base substitution C T upstream_gene_variant MELA-AU X 53712588 53712588 single base substitution G A intron_variant MELA-AU X 53712588 53712588 single base substitution G A upstream_gene_variant MELA-AU X 53712848 53712848 single base substitution C T intron_variant MELA-AU X 53712848 53712848 single base substitution C T upstream_gene_variant MELA-AU X 53715231 53715231 single base substitution C T upstream_gene_variant MELA-AU X 53715798 53715798 single base substitution C T upstream_gene_variant MELA-AU X 53715819 53715819 single base substitution C T upstream_gene_variant MELA-AU X 53715975 53715975 single base substitution C T upstream_gene_variant MELA-AU X 53716000 53716000 single base substitution C T upstream_gene_variant MELA-AU X 53716154 53716154 single base substitution A G upstream_gene_variant MELA-AU X 53717814 53717814 single base substitution T G upstream_gene_variant MELA-AU X 53718324 53718324 single base substitution C T upstream_gene_variant ORCA-IN X 53561566 53561566 single base substitution C T downstream_gene_variant ORCA-IN X 53561566 53561566 single base substitution C T exon_variant ORCA-IN X 53561566 53561566 single base substitution C T missense_variant E1070K 3208G>A ORCA-IN X 53561566 53561566 single base substitution C T missense_variant E3281K 9841G>A ORCA-IN X 53561566 53561566 single base substitution C T missense_variant E4248K 12742G>A ORCA-IN X 53562615 53562615 single base substitution C A downstream_gene_variant ORCA-IN X 53562615 53562615 single base substitution C A intron_variant ORCA-IN X 53562615 53562615 single base substitution C A upstream_gene_variant ORCA-IN X 53563206 53563206 single base substitution C T downstream_gene_variant ORCA-IN X 53563206 53563206 single base substitution C T exon_variant ORCA-IN X 53563206 53563206 single base substitution C T missense_variant D3178N 9532G>A ORCA-IN X 53563206 53563206 single base substitution C T missense_variant D4145N 12433G>A ORCA-IN X 53563206 53563206 single base substitution C T missense_variant D967N 2899G>A ORCA-IN X 53563206 53563206 single base substitution C T upstream_gene_variant ORCA-IN X 53565382 53565382 single base substitution C A downstream_gene_variant ORCA-IN X 53565382 53565382 single base substitution C A exon_variant ORCA-IN X 53565382 53565382 single base substitution C A missense_variant R3004L 9011G>T ORCA-IN X 53565382 53565382 single base substitution C A missense_variant R3971L 11912G>T ORCA-IN X 53565382 53565382 single base substitution C A missense_variant R793L 2378G>T ORCA-IN X 53565382 53565382 single base substitution C A upstream_gene_variant ORCA-IN X 53565410 53565410 single base substitution G C downstream_gene_variant ORCA-IN X 53565410 53565410 single base substitution G C exon_variant ORCA-IN X 53565410 53565410 single base substitution G C missense_variant H2995D 8983C>G ORCA-IN X 53565410 53565410 single base substitution G C missense_variant H3962D 11884C>G ORCA-IN X 53565410 53565410 single base substitution G C missense_variant H784D 2350C>G ORCA-IN X 53565410 53565410 single base substitution G C upstream_gene_variant ORCA-IN X 53570452 53570452 single base substitution G C downstream_gene_variant ORCA-IN X 53570452 53570452 single base substitution G C intron_variant ORCA-IN X 53570452 53570452 single base substitution G C upstream_gene_variant ORCA-IN X 53571560 53571560 single base substitution G T exon_variant ORCA-IN X 53571560 53571560 single base substitution G T intron_variant ORCA-IN X 53571560 53571560 single base substitution G T missense_variant R2771S 8311C>A ORCA-IN X 53571560 53571560 single base substitution G T missense_variant R3738S 11212C>A ORCA-IN X 53571560 53571560 single base substitution G T missense_variant R575S 1723C>A ORCA-IN X 53571560 53571560 single base substitution G T upstream_gene_variant ORCA-IN X 53588834 53588834 single base substitution C T missense_variant E1497K 4489G>A ORCA-IN X 53588834 53588834 single base substitution C T missense_variant E2464K 7390G>A ORCA-IN X 53589074 53589074 single base substitution G A stop_gained Q1479* 4435C>T ORCA-IN X 53589074 53589074 single base substitution G A stop_gained Q2446* 7336C>T ORCA-IN X 53589206 53589206 single base substitution C G splice_acceptor_variant ORCA-IN X 53591546 53591546 single base substitution G T missense_variant Q1373K 4117C>A ORCA-IN X 53591546 53591546 single base substitution G T missense_variant Q2340K 7018C>A ORCA-IN X 53617444 53617444 single base substitution C T missense_variant E1371K 4111G>A ORCA-IN X 53617444 53617444 single base substitution C T missense_variant E404K 1210G>A ORCA-IN X 53631792 53631792 single base substitution G T missense_variant L834M 2500C>A ORCA-IN X 53631792 53631792 single base substitution G T upstream_gene_variant ORCA-IN X 53654360 53654360 single base substitution C A downstream_gene_variant ORCA-IN X 53654360 53654360 single base substitution C A splice_donor_variant ORCA-IN X 53654360 53654360 single base substitution C A upstream_gene_variant ORCA-IN X 53672314 53672314 single base substitution C T downstream_gene_variant ORCA-IN X 53672314 53672314 single base substitution C T synonymous_variant L151L 453G>A ORCA-IN X 53677396 53677396 single base substitution G A intron_variant ORCA-IN X 53701769 53701769 single base substitution C G intron_variant ORCA-IN X 53702098 53702098 single base substitution G C intron_variant OV-AU X 53554851 53554851 single base substitution C T downstream_gene_variant OV-AU X 53558057 53558057 single base substitution G C downstream_gene_variant OV-AU X 53563073 53563073 single base substitution C A downstream_gene_variant OV-AU X 53563073 53563073 single base substitution C A exon_variant OV-AU X 53563073 53563073 single base substitution C A intron_variant OV-AU X 53563073 53563073 single base substitution C A upstream_gene_variant OV-AU X 53568853 53568853 single base substitution C G downstream_gene_variant OV-AU X 53568853 53568853 single base substitution C G intron_variant OV-AU X 53568853 53568853 single base substitution C G upstream_gene_variant OV-AU X 53569864 53569864 single base substitution C T downstream_gene_variant OV-AU X 53569864 53569864 single base substitution C T intron_variant OV-AU X 53569864 53569864 single base substitution C T upstream_gene_variant OV-AU X 53580168 53580168 single base substitution A T intron_variant OV-AU X 53580168 53580168 single base substitution A T upstream_gene_variant OV-AU X 53587409 53587409 single base substitution C T intron_variant OV-AU X 53591637 53591637 single base substitution A T synonymous_variant T1342T 4026T>A OV-AU X 53591637 53591637 single base substitution A T synonymous_variant T2309T 6927T>A OV-AU X 53599794 53599794 single base substitution C T intron_variant OV-AU X 53602507 53602507 single base substitution T C intron_variant OV-AU X 53615291 53615291 single base substitution T A intron_variant OV-AU X 53617507 53617507 single base substitution G C intron_variant OV-AU X 53619105 53619105 single base substitution C A intron_variant OV-AU X 53620624 53620624 single base substitution C T intron_variant OV-AU X 53628691 53628691 single base substitution C T intron_variant OV-AU X 53632718 53632718 single base substitution C G intron_variant OV-AU X 53632718 53632718 single base substitution C G upstream_gene_variant OV-AU X 53641281 53641281 single base substitution C G downstream_gene_variant OV-AU X 53641281 53641281 single base substitution C G intron_variant OV-AU X 53642776 53642776 single base substitution C T exon_variant OV-AU X 53642776 53642776 single base substitution C T missense_variant G660R 1978G>A OV-AU X 53645496 53645496 single base substitution A G intron_variant OV-AU X 53650616 53650616 single base substitution A T downstream_gene_variant OV-AU X 53650616 53650616 single base substitution A T intron_variant OV-AU X 53652328 53652328 single base substitution A G exon_variant OV-AU X 53652328 53652328 single base substitution A G intron_variant OV-AU X 53654648 53654648 single base substitution G A downstream_gene_variant OV-AU X 53654648 53654648 single base substitution G A intron_variant OV-AU X 53654648 53654648 single base substitution G A upstream_gene_variant OV-AU X 53660451 53660451 single base substitution G A intron_variant OV-AU X 53660451 53660451 single base substitution G A upstream_gene_variant OV-AU X 53661021 53661021 single base substitution G C intron_variant OV-AU X 53661021 53661021 single base substitution G C upstream_gene_variant OV-AU X 53663486 53663486 single base substitution C G intron_variant OV-AU X 53663486 53663486 single base substitution C G upstream_gene_variant OV-AU X 53694081 53694081 single base substitution A G intron_variant OV-AU X 53701377 53701377 single base substitution T C intron_variant OV-AU X 53702950 53702950 single base substitution A T intron_variant OV-AU X 53705582 53705582 single base substitution T G intron_variant OV-AU X 53710735 53710735 single base substitution G T intron_variant OV-AU X 53717303 53717303 single base substitution T C upstream_gene_variant OV-US X 53577911 53577911 single base substitution C G synonymous_variant L2145L 6435G>C OV-US X 53577911 53577911 single base substitution C G synonymous_variant L3112L 9336G>C OV-US X 53577911 53577911 single base substitution C G upstream_gene_variant OV-US X 53578151 53578151 single base substitution C A splice_acceptor_variant OV-US X 53578151 53578151 single base substitution C A upstream_gene_variant PACA-AU X 53561496 53561496 single base substitution T C downstream_gene_variant PACA-AU X 53561496 53561496 single base substitution T C exon_variant PACA-AU X 53561496 53561496 single base substitution T C missense_variant Y1093C 3278A>G PACA-AU X 53561496 53561496 single base substitution T C missense_variant Y3304C 9911A>G PACA-AU X 53561496 53561496 single base substitution T C missense_variant Y4271C 12812A>G PACA-AU X 53562355 53562355 single base substitution C T downstream_gene_variant PACA-AU X 53562355 53562355 single base substitution C T missense_variant M1035I 3105G>A PACA-AU X 53562355 53562355 single base substitution C T missense_variant M3246I 9738G>A PACA-AU X 53562355 53562355 single base substitution C T missense_variant M4213I 12639G>A PACA-AU X 53562355 53562355 single base substitution C T upstream_gene_variant PACA-AU X 53563408 53563408 single base substitution C T downstream_gene_variant PACA-AU X 53563408 53563408 single base substitution C T exon_variant PACA-AU X 53563408 53563408 single base substitution C T missense_variant D3153N 9457G>A PACA-AU X 53563408 53563408 single base substitution C T missense_variant D4120N 12358G>A PACA-AU X 53563408 53563408 single base substitution C T missense_variant D942N 2824G>A PACA-AU X 53563408 53563408 single base substitution C T upstream_gene_variant PACA-AU X 53568124 53568124 single base substitution C G downstream_gene_variant PACA-AU X 53568124 53568124 single base substitution C G intron_variant PACA-AU X 53568124 53568124 single base substitution C G upstream_gene_variant PACA-AU X 53574519 53574519 single base substitution C G intron_variant PACA-AU X 53574519 53574519 single base substitution C G upstream_gene_variant PACA-AU X 53576502 53576502 single base substitution G A intron_variant PACA-AU X 53576502 53576502 single base substitution G A upstream_gene_variant PACA-AU X 53577703 53577703 single base substitution G A missense_variant R2171C 6511C>T PACA-AU X 53577703 53577703 single base substitution G A missense_variant R3138C 9412C>T PACA-AU X 53577703 53577703 single base substitution G A upstream_gene_variant PACA-AU X 53578764 53578764 single base substitution G A intron_variant PACA-AU X 53578764 53578764 single base substitution G A upstream_gene_variant PACA-AU X 53593075 53593075 insertion of <=200bp - TGTG intron_variant PACA-AU X 53593082 53593082 single base substitution G A intron_variant PACA-AU X 53593095 53593095 insertion of <=200bp - TGTA intron_variant PACA-AU X 53594000 53594000 single base substitution T C intron_variant PACA-AU X 53597720 53597720 insertion of <=200bp - T intron_variant PACA-AU X 53599917 53599917 single base substitution A G intron_variant PACA-AU X 53608978 53608978 single base substitution C T downstream_gene_variant PACA-AU X 53608978 53608978 single base substitution C T intron_variant PACA-AU X 53624991 53624991 single base substitution T C intron_variant PACA-AU X 53644410 53644410 deletion of <=200bp A - splice_region_variant PACA-AU X 53657638 53657638 single base substitution A G downstream_gene_variant PACA-AU X 53657638 53657638 single base substitution A G intron_variant PACA-AU X 53657638 53657638 single base substitution A G upstream_gene_variant PACA-AU X 53659378 53659378 single base substitution G A intron_variant PACA-AU X 53659378 53659378 single base substitution G A upstream_gene_variant PACA-AU X 53667048 53667048 single base substitution C T intron_variant PACA-AU X 53668558 53668558 single base substitution A C intron_variant PACA-AU X 53671713 53671713 single base substitution C G downstream_gene_variant PACA-AU X 53671713 53671713 single base substitution C G intron_variant PACA-AU X 53674514 53674514 single base substitution C T missense_variant E50K 148G>A PACA-AU X 53681226 53681226 single base substitution C G intron_variant PACA-AU X 53681513 53681513 single base substitution A G intron_variant PACA-AU X 53682723 53682723 single base substitution G A intron_variant PACA-AU X 53686577 53686579 deletion of <=200bp TGT - intron_variant PACA-AU X 53696982 53696990 deletion of <=200bp ACAAGCAGG - intron_variant PACA-AU X 53698299 53698299 single base substitution T C intron_variant PACA-AU X 53699214 53699214 single base substitution C T intron_variant PACA-CA X 53554609 53554609 single base substitution C T downstream_gene_variant PACA-CA X 53556213 53556213 single base substitution G A downstream_gene_variant PACA-CA X 53572280 53572280 single base substitution G A intron_variant PACA-CA X 53572280 53572280 single base substitution G A upstream_gene_variant PACA-CA X 53574096 53574096 single base substitution T G intron_variant PACA-CA X 53574096 53574096 single base substitution T G upstream_gene_variant PACA-CA X 53575787 53575787 single base substitution C A intron_variant PACA-CA X 53575787 53575787 single base substitution C A upstream_gene_variant PACA-CA X 53584370 53584370 single base substitution T C missense_variant N1760D 5278A>G PACA-CA X 53584370 53584370 single base substitution T C missense_variant N2727D 8179A>G PACA-CA X 53591253 53591253 single base substitution G A intron_variant PACA-CA X 53598558 53598558 deletion of <=200bp A - intron_variant PACA-CA X 53610957 53610957 single base substitution C T downstream_gene_variant PACA-CA X 53610957 53610957 single base substitution C T intron_variant PACA-CA X 53612705 53612705 single base substitution G A intron_variant PACA-CA X 53613492 53613492 single base substitution T C synonymous_variant E1594E 4782A>G PACA-CA X 53613492 53613492 single base substitution T C synonymous_variant E627E 1881A>G PACA-CA X 53613871 53613871 single base substitution T C splice_acceptor_variant PACA-CA X 53617566 53617566 single base substitution G A intron_variant PACA-CA X 53621056 53621056 insertion of <=200bp - A intron_variant PACA-CA X 53623824 53623824 single base substitution C T intron_variant PACA-CA X 53625204 53625204 insertion of <=200bp - T intron_variant PACA-CA X 53625889 53625889 single base substitution C T intron_variant PACA-CA X 53627384 53627384 single base substitution G A intron_variant PACA-CA X 53629815 53629815 single base substitution C T intron_variant PACA-CA X 53629906 53629906 single base substitution G A intron_variant PACA-CA X 53629969 53629969 single base substitution C T intron_variant PACA-CA X 53634403 53634403 single base substitution C A intron_variant PACA-CA X 53634403 53634403 single base substitution C A upstream_gene_variant PACA-CA X 53637977 53637977 single base substitution A G downstream_gene_variant PACA-CA X 53637977 53637977 single base substitution A G intron_variant PACA-CA X 53638828 53638828 single base substitution A T downstream_gene_variant PACA-CA X 53638828 53638828 single base substitution A T intron_variant PACA-CA X 53642063 53642063 single base substitution C G downstream_gene_variant PACA-CA X 53642063 53642063 single base substitution C G intron_variant PACA-CA X 53642397 53642397 single base substitution C A downstream_gene_variant PACA-CA X 53642397 53642397 single base substitution C A intron_variant PACA-CA X 53649082 53649082 single base substitution C A downstream_gene_variant PACA-CA X 53649082 53649082 single base substitution C A intron_variant PACA-CA X 53654518 53654518 single base substitution A T downstream_gene_variant PACA-CA X 53654518 53654518 single base substitution A T intron_variant PACA-CA X 53654518 53654518 single base substitution A T upstream_gene_variant PACA-CA X 53656382 53656382 insertion of <=200bp - C downstream_gene_variant PACA-CA X 53656382 53656382 insertion of <=200bp - C intron_variant PACA-CA X 53656382 53656382 insertion of <=200bp - C upstream_gene_variant PACA-CA X 53657847 53657847 single base substitution T A exon_variant PACA-CA X 53657847 53657847 single base substitution T A intron_variant PACA-CA X 53657847 53657847 single base substitution T A upstream_gene_variant PACA-CA X 53662826 53662826 single base substitution T C intron_variant PACA-CA X 53662826 53662826 single base substitution T C upstream_gene_variant PACA-CA X 53665291 53665291 insertion of <=200bp - A intron_variant PACA-CA X 53669417 53669417 single base substitution T C downstream_gene_variant PACA-CA X 53669417 53669417 single base substitution T C intron_variant PACA-CA X 53670492 53670492 single base substitution T C downstream_gene_variant PACA-CA X 53670492 53670492 single base substitution T C intron_variant PACA-CA X 53680779 53680779 single base substitution C T intron_variant PACA-CA X 53683505 53683505 single base substitution A G intron_variant PACA-CA X 53683554 53683554 single base substitution G T intron_variant PACA-CA X 53688292 53688292 insertion of <=200bp - T intron_variant PACA-CA X 53690415 53690415 single base substitution C T intron_variant PACA-CA X 53690996 53690996 single base substitution T G intron_variant PACA-CA X 53692360 53692360 single base substitution T G intron_variant PACA-CA X 53697177 53697177 single base substitution A C intron_variant PACA-CA X 53697656 53697656 single base substitution A T intron_variant PACA-CA X 53708867 53708867 single base substitution C T intron_variant PACA-CA X 53712171 53712171 insertion of <=200bp - T intron_variant PACA-CA X 53712171 53712171 insertion of <=200bp - T upstream_gene_variant PACA-CA X 53715249 53715249 insertion of <=200bp - T upstream_gene_variant PACA-CA X 53716257 53716257 single base substitution A G upstream_gene_variant PACA-CA X 53717906 53717906 deletion of <=200bp C - upstream_gene_variant PAEN-AU X 53557690 53557690 single base substitution C A downstream_gene_variant PAEN-AU X 53583759 53583759 single base substitution C T intron_variant PAEN-AU X 53638784 53638784 single base substitution A C downstream_gene_variant PAEN-AU X 53638784 53638784 single base substitution A C intron_variant PAEN-AU X 53683351 53683351 single base substitution T G intron_variant PAEN-AU X 53704947 53704947 single base substitution C G intron_variant PAEN-IT X 53597336 53597336 single base substitution T C intron_variant PAEN-IT X 53629835 53629835 single base substitution C G intron_variant PAEN-IT X 53632176 53632176 single base substitution T C intron_variant PAEN-IT X 53632176 53632176 single base substitution T C upstream_gene_variant PAEN-IT X 53638441 53638441 single base substitution A G downstream_gene_variant PAEN-IT X 53638441 53638441 single base substitution A G intron_variant PBCA-DE X 53554729 53554729 single base substitution T C downstream_gene_variant PBCA-DE X 53557408 53557408 deletion of <=200bp T - downstream_gene_variant PBCA-DE X 53562252 53562252 single base substitution A G downstream_gene_variant PBCA-DE X 53562252 53562252 single base substitution A G intron_variant PBCA-DE X 53562252 53562252 single base substitution A G upstream_gene_variant PBCA-DE X 53564100 53564100 single base substitution G A downstream_gene_variant PBCA-DE X 53564100 53564100 single base substitution G A intron_variant PBCA-DE X 53564100 53564100 single base substitution G A upstream_gene_variant PBCA-DE X 53567466 53567466 single base substitution T G downstream_gene_variant PBCA-DE X 53567466 53567466 single base substitution T G intron_variant PBCA-DE X 53567466 53567466 single base substitution T G upstream_gene_variant PBCA-DE X 53568658 53568658 single base substitution T A downstream_gene_variant PBCA-DE X 53568658 53568658 single base substitution T A intron_variant PBCA-DE X 53568658 53568658 single base substitution T A upstream_gene_variant PBCA-DE X 53577153 53577153 insertion of <=200bp - GGTA intron_variant PBCA-DE X 53577153 53577153 insertion of <=200bp - GGTA upstream_gene_variant PBCA-DE X 53583345 53583345 single base substitution G C intron_variant PBCA-DE X 53586500 53586500 single base substitution G A splice_region_variant PBCA-DE X 53588765 53588765 single base substitution G A missense_variant R1520W 4558C>T PBCA-DE X 53588765 53588765 single base substitution G A missense_variant R2487W 7459C>T PBCA-DE X 53593433 53593433 single base substitution G A intron_variant PBCA-DE X 53610953 53610953 single base substitution T C downstream_gene_variant PBCA-DE X 53610953 53610953 single base substitution T C intron_variant PBCA-DE X 53618491 53618491 single base substitution G T intron_variant PBCA-DE X 53627217 53627217 single base substitution T A missense_variant L1008F 3024A>T PBCA-DE X 53627217 53627217 single base substitution T A missense_variant L41F 123A>T PBCA-DE X 53627905 53627905 single base substitution T A intron_variant PBCA-DE X 53629879 53629879 deletion of <=200bp T - intron_variant PBCA-DE X 53635113 53635113 insertion of <=200bp - T intron_variant PBCA-DE X 53635113 53635113 insertion of <=200bp - T upstream_gene_variant PBCA-DE X 53640524 53640524 single base substitution A G downstream_gene_variant PBCA-DE X 53640524 53640524 single base substitution A G intron_variant PBCA-DE X 53645307 53645307 single base substitution T A intron_variant PBCA-DE X 53650325 53650325 deletion of <=200bp A - downstream_gene_variant PBCA-DE X 53650325 53650325 deletion of <=200bp A - intron_variant PBCA-DE X 53652838 53652838 single base substitution G A downstream_gene_variant PBCA-DE X 53652838 53652838 single base substitution G A intron_variant PBCA-DE X 53652838 53652838 single base substitution G A synonymous_variant P144P 432C>T PBCA-DE X 53652838 53652838 single base substitution G A upstream_gene_variant PBCA-DE X 53654501 53654502 deletion of <=200bp TA - downstream_gene_variant PBCA-DE X 53654501 53654502 deletion of <=200bp TA - intron_variant PBCA-DE X 53654501 53654502 deletion of <=200bp TA - upstream_gene_variant PBCA-DE X 53656077 53656077 single base substitution A G downstream_gene_variant PBCA-DE X 53656077 53656077 single base substitution A G intron_variant PBCA-DE X 53656077 53656077 single base substitution A G upstream_gene_variant PBCA-DE X 53656390 53656390 single base substitution C A downstream_gene_variant PBCA-DE X 53656390 53656390 single base substitution C A intron_variant PBCA-DE X 53656390 53656390 single base substitution C A upstream_gene_variant PBCA-DE X 53658298 53658298 single base substitution C A intron_variant PBCA-DE X 53658298 53658298 single base substitution C A upstream_gene_variant PBCA-DE X 53666448 53666448 single base substitution G A intron_variant PBCA-DE X 53678958 53678958 single base substitution C T intron_variant PBCA-DE X 53689872 53689872 insertion of <=200bp - G intron_variant PBCA-DE X 53692003 53692003 single base substitution T C intron_variant PBCA-DE X 53694450 53694450 single base substitution C A intron_variant PBCA-DE X 53707627 53707627 deletion of <=200bp C - 5_prime_UTR_variant PBCA-DE X 53707627 53707627 deletion of <=200bp C - intron_variant PBCA-DE X 53713020 53713021 deletion of <=200bp TG - intron_variant PBCA-DE X 53713020 53713021 deletion of <=200bp TG - upstream_gene_variant PBCA-DE X 53713616 53713616 single base substitution C T 5_prime_UTR_variant PBCA-DE X 53713616 53713616 single base substitution C T upstream_gene_variant PBCA-DE X 53718247 53718247 single base substitution C A upstream_gene_variant PRAD-CA X 53555782 53555782 single base substitution G C downstream_gene_variant PRAD-CA X 53558543 53558543 single base substitution A C downstream_gene_variant PRAD-CA X 53565683 53565683 single base substitution A T downstream_gene_variant PRAD-CA X 53565683 53565683 single base substitution A T intron_variant PRAD-CA X 53565683 53565683 single base substitution A T upstream_gene_variant PRAD-CA X 53593096 53593096 single base substitution A G intron_variant PRAD-CA X 53593098 53593098 single base substitution A G intron_variant PRAD-CA X 53610811 53610811 single base substitution C A downstream_gene_variant PRAD-CA X 53610811 53610811 single base substitution C A missense_variant G1743W 5227G>T PRAD-CA X 53610811 53610811 single base substitution C A missense_variant G776W 2326G>T PRAD-CA X 53612715 53612715 single base substitution C T intron_variant PRAD-CA X 53666672 53666672 single base substitution A C intron_variant PRAD-CA X 53688811 53688811 single base substitution T A intron_variant PRAD-CA X 53703126 53703126 single base substitution T C intron_variant PRAD-UK X 53554331 53554331 single base substitution C G downstream_gene_variant PRAD-UK X 53623340 53623340 single base substitution A G intron_variant PRAD-UK X 53631410 53631410 single base substitution A C intron_variant PRAD-UK X 53631410 53631410 single base substitution A C upstream_gene_variant PRAD-UK X 53635112 53635112 single base substitution A T intron_variant PRAD-UK X 53635112 53635112 single base substitution A T upstream_gene_variant PRAD-UK X 53636790 53636790 single base substitution A C intron_variant PRAD-UK X 53640564 53640564 single base substitution T C downstream_gene_variant PRAD-UK X 53640564 53640564 single base substitution T C intron_variant PRAD-UK X 53665279 53665279 single base substitution G T intron_variant PRAD-UK X 53666512 53666512 single base substitution A C intron_variant PRAD-UK X 53709238 53709238 single base substitution A C intron_variant PRAD-UK X 53716181 53716181 single base substitution G T upstream_gene_variant PRAD-US X 53578098 53578098 single base substitution G A missense_variant A2083V 6248C>T PRAD-US X 53578098 53578098 single base substitution G A missense_variant A3050V 9149C>T PRAD-US X 53578098 53578098 single base substitution G A upstream_gene_variant PRAD-US X 53618049 53618049 single base substitution T C missense_variant M1336V 4006A>G PRAD-US X 53618049 53618049 single base substitution T C missense_variant M369V 1105A>G PRAD-US X 53657925 53657925 single base substitution T C exon_variant PRAD-US X 53657925 53657925 single base substitution T C missense_variant Q275R 824A>G PRAD-US X 53657925 53657925 single base substitution T C upstream_gene_variant READ-US X 53577717 53577717 single base substitution C T missense_variant R2166H 6497G>A READ-US X 53577717 53577717 single base substitution C T missense_variant R3133H 9398G>A READ-US X 53577717 53577717 single base substitution C T upstream_gene_variant READ-US X 53587180 53587180 single base substitution G A missense_variant R1602C 4804C>T READ-US X 53587180 53587180 single base substitution G A missense_variant R2569C 7705C>T READ-US X 53610679 53610679 single base substitution G A downstream_gene_variant READ-US X 53610679 53610679 single base substitution G A missense_variant R1787W 5359C>T READ-US X 53610679 53610679 single base substitution G A missense_variant R820W 2458C>T READ-US X 53616547 53616547 single base substitution G C missense_variant A1474G 4421C>G READ-US X 53616547 53616547 single base substitution G C missense_variant A507G 1520C>G RECA-EU X 53559370 53559370 single base substitution T A 3_prime_UTR_variant RECA-EU X 53559370 53559370 single base substitution T A downstream_gene_variant RECA-EU X 53564820 53564820 single base substitution A G downstream_gene_variant RECA-EU X 53564820 53564820 single base substitution A G intron_variant RECA-EU X 53564820 53564820 single base substitution A G upstream_gene_variant RECA-EU X 53565710 53565710 single base substitution C G downstream_gene_variant RECA-EU X 53565710 53565710 single base substitution C G intron_variant RECA-EU X 53565710 53565710 single base substitution C G upstream_gene_variant RECA-EU X 53577155 53577155 single base substitution G C intron_variant RECA-EU X 53577155 53577155 single base substitution G C upstream_gene_variant RECA-EU X 53579517 53579517 single base substitution T A intron_variant RECA-EU X 53579517 53579517 single base substitution T A upstream_gene_variant RECA-EU X 53585186 53585186 single base substitution T A intron_variant RECA-EU X 53589559 53589559 single base substitution G C intron_variant RECA-EU X 53590937 53590937 single base substitution C G intron_variant RECA-EU X 53596381 53596381 single base substitution T A intron_variant RECA-EU X 53621189 53621189 single base substitution A T intron_variant RECA-EU X 53623468 53623468 single base substitution T C intron_variant RECA-EU X 53632714 53632714 single base substitution C A intron_variant RECA-EU X 53632714 53632714 single base substitution C A upstream_gene_variant RECA-EU X 53633560 53633560 single base substitution G A intron_variant RECA-EU X 53633560 53633560 single base substitution G A upstream_gene_variant RECA-EU X 53655266 53655266 single base substitution A T downstream_gene_variant RECA-EU X 53655266 53655266 single base substitution A T intron_variant RECA-EU X 53655266 53655266 single base substitution A T upstream_gene_variant RECA-EU X 53675684 53675684 single base substitution G A intron_variant RECA-EU X 53708862 53708862 single base substitution G T intron_variant SKCA-BR X 53558390 53558390 single base substitution G A downstream_gene_variant SKCA-BR X 53558534 53558534 single base substitution G A downstream_gene_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACTCT downstream_gene_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACTCT intron_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACTCT upstream_gene_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACT downstream_gene_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACT intron_variant SKCA-BR X 53565683 53565683 insertion of <=200bp - ACT upstream_gene_variant SKCA-BR X 53567182 53567182 single base substitution G A downstream_gene_variant SKCA-BR X 53567182 53567182 single base substitution G A intron_variant SKCA-BR X 53567182 53567182 single base substitution G A upstream_gene_variant SKCA-BR X 53572158 53572158 single base substitution C T intron_variant SKCA-BR X 53572158 53572158 single base substitution C T upstream_gene_variant SKCA-BR X 53574895 53574895 single base substitution G A exon_variant SKCA-BR X 53574895 53574895 single base substitution G A missense_variant L2492F 7474C>T SKCA-BR X 53574895 53574895 single base substitution G A missense_variant L296F 886C>T SKCA-BR X 53574895 53574895 single base substitution G A missense_variant L3459F 10375C>T SKCA-BR X 53574895 53574895 single base substitution G A upstream_gene_variant SKCA-BR X 53579198 53579198 single base substitution G A intron_variant SKCA-BR X 53579198 53579198 single base substitution G A upstream_gene_variant SKCA-BR X 53587415 53587415 single base substitution G A intron_variant SKCA-BR X 53587457 53587457 single base substitution G A intron_variant SKCA-BR X 53592742 53592742 single base substitution G A intron_variant SKCA-BR X 53593096 53593096 single base substitution A G intron_variant SKCA-BR X 53596718 53596718 single base substitution T G missense_variant T1161P 3481A>C SKCA-BR X 53596718 53596718 single base substitution T G missense_variant T2128P 6382A>C SKCA-BR X 53596777 53596777 single base substitution A C missense_variant V1141G 3422T>G SKCA-BR X 53596777 53596777 single base substitution A C missense_variant V2108G 6323T>G SKCA-BR X 53601121 53601121 single base substitution G A intron_variant SKCA-BR X 53603385 53603385 single base substitution G A intron_variant SKCA-BR X 53604716 53604716 single base substitution G A intron_variant SKCA-BR X 53611583 53611583 single base substitution G A intron_variant SKCA-BR X 53615212 53615212 single base substitution A T intron_variant SKCA-BR X 53616312 53616312 single base substitution C T intron_variant SKCA-BR X 53616737 53616737 single base substitution G A missense_variant R1411W 4231C>T SKCA-BR X 53616737 53616737 single base substitution G A missense_variant R444W 1330C>T SKCA-BR X 53617832 53617832 single base substitution G A intron_variant SKCA-BR X 53623739 53623739 single base substitution T C intron_variant SKCA-BR X 53629294 53629294 insertion of <=200bp - GT intron_variant SKCA-BR X 53632244 53632244 single base substitution G A intron_variant SKCA-BR X 53632244 53632244 single base substitution G A upstream_gene_variant SKCA-BR X 53633590 53633590 single base substitution G A intron_variant SKCA-BR X 53633590 53633590 single base substitution G A upstream_gene_variant SKCA-BR X 53633591 53633591 single base substitution G A intron_variant SKCA-BR X 53633591 53633591 single base substitution G A upstream_gene_variant SKCA-BR X 53635311 53635311 single base substitution G A intron_variant SKCA-BR X 53635311 53635311 single base substitution G A upstream_gene_variant SKCA-BR X 53636399 53636399 single base substitution G A intron_variant SKCA-BR X 53637792 53637792 single base substitution C T downstream_gene_variant SKCA-BR X 53637792 53637792 single base substitution C T intron_variant SKCA-BR X 53639415 53639415 single base substitution G A downstream_gene_variant SKCA-BR X 53639415 53639415 single base substitution G A intron_variant SKCA-BR X 53641880 53641880 single base substitution G A downstream_gene_variant SKCA-BR X 53641880 53641880 single base substitution G A intron_variant SKCA-BR X 53642043 53642043 single base substitution T G downstream_gene_variant SKCA-BR X 53642043 53642043 single base substitution T G intron_variant SKCA-BR X 53647258 53647258 single base substitution C T downstream_gene_variant SKCA-BR X 53647258 53647258 single base substitution C T intron_variant SKCA-BR X 53649165 53649165 single base substitution C G downstream_gene_variant SKCA-BR X 53649165 53649165 single base substitution C G intron_variant SKCA-BR X 53651399 53651399 single base substitution A G downstream_gene_variant SKCA-BR X 53651399 53651399 single base substitution A G intron_variant SKCA-BR X 53653171 53653173 deletion of <=200bp CGT - downstream_gene_variant SKCA-BR X 53653171 53653173 deletion of <=200bp CGT - intron_variant SKCA-BR X 53653171 53653173 deletion of <=200bp CGT - upstream_gene_variant SKCA-BR X 53654828 53654828 single base substitution G A downstream_gene_variant SKCA-BR X 53654828 53654828 single base substitution G A splice_region_variant SKCA-BR X 53654828 53654828 single base substitution G A upstream_gene_variant SKCA-BR X 53660378 53660378 single base substitution G A intron_variant SKCA-BR X 53660378 53660378 single base substitution G A upstream_gene_variant SKCA-BR X 53664481 53664481 single base substitution C T intron_variant SKCA-BR X 53669326 53669326 single base substitution G A intron_variant SKCA-BR X 53669531 53669531 single base substitution T A downstream_gene_variant SKCA-BR X 53669531 53669531 single base substitution T A intron_variant SKCA-BR X 53672168 53672168 single base substitution G A downstream_gene_variant SKCA-BR X 53672168 53672168 single base substitution G A intron_variant SKCA-BR X 53673323 53673323 single base substitution A C downstream_gene_variant SKCA-BR X 53673323 53673323 single base substitution A C intron_variant SKCA-BR X 53683181 53683181 single base substitution G A intron_variant SKCA-BR X 53683533 53683533 single base substitution G A intron_variant SKCA-BR X 53685352 53685352 single base substitution G A intron_variant SKCA-BR X 53690296 53690296 single base substitution G C intron_variant SKCA-BR X 53695478 53695478 single base substitution A G intron_variant SKCA-BR X 53696217 53696217 single base substitution G A intron_variant SKCA-BR X 53699524 53699524 single base substitution C T intron_variant SKCA-BR X 53700005 53700005 single base substitution A C intron_variant SKCA-BR X 53702506 53702506 single base substitution T C intron_variant SKCA-BR X 53708844 53708844 single base substitution T G intron_variant SKCA-BR X 53709574 53709574 single base substitution G A intron_variant SKCA-BR X 53713601 53713601 single base substitution C T 5_prime_UTR_variant SKCA-BR X 53713601 53713601 single base substitution C T upstream_gene_variant SKCA-BR X 53713787 53713787 single base substitution G A upstream_gene_variant SKCA-BR X 53713941 53713941 single base substitution T A upstream_gene_variant SKCA-BR X 53714177 53714177 single base substitution A G upstream_gene_variant SKCA-BR X 53715287 53715287 single base substitution C T upstream_gene_variant SKCA-BR X 53715373 53715374 deletion of <=200bp AT - upstream_gene_variant SKCA-BR X 53716187 53716187 single base substitution G A upstream_gene_variant SKCM-US X 53563540 53563540 single base substitution G A downstream_gene_variant SKCM-US X 53563540 53563540 single base substitution G A exon_variant SKCM-US X 53563540 53563540 single base substitution G A missense_variant P3109S 9325C>T SKCM-US X 53563540 53563540 single base substitution G A missense_variant P4076S 12226C>T SKCM-US X 53563540 53563540 single base substitution G A missense_variant P898S 2692C>T SKCM-US X 53563540 53563540 single base substitution G A upstream_gene_variant SKCM-US X 53563559 53563559 single base substitution G A downstream_gene_variant SKCM-US X 53563559 53563559 single base substitution G A exon_variant SKCM-US X 53563559 53563559 single base substitution G A synonymous_variant I3102I 9306C>T SKCM-US X 53563559 53563559 single base substitution G A synonymous_variant I4069I 12207C>T SKCM-US X 53563559 53563559 single base substitution G A synonymous_variant I891I 2673C>T SKCM-US X 53563559 53563559 single base substitution G A upstream_gene_variant SKCM-US X 53564540 53564540 single base substitution G A downstream_gene_variant SKCM-US X 53564540 53564540 single base substitution G A exon_variant SKCM-US X 53564540 53564540 single base substitution G A synonymous_variant S3071S 9213C>T SKCM-US X 53564540 53564540 single base substitution G A synonymous_variant S4038S 12114C>T SKCM-US X 53564540 53564540 single base substitution G A synonymous_variant S860S 2580C>T SKCM-US X 53564540 53564540 single base substitution G A upstream_gene_variant SKCM-US X 53564554 53564554 single base substitution G A downstream_gene_variant SKCM-US X 53564554 53564554 single base substitution G A exon_variant SKCM-US X 53564554 53564554 single base substitution G A synonymous_variant L3067L 9199C>T SKCM-US X 53564554 53564554 single base substitution G A synonymous_variant L4034L 12100C>T SKCM-US X 53564554 53564554 single base substitution G A synonymous_variant L856L 2566C>T SKCM-US X 53564554 53564554 single base substitution G A upstream_gene_variant SKCM-US X 53565956 53565956 single base substitution G A downstream_gene_variant SKCM-US X 53565956 53565956 single base substitution G A synonymous_variant S2939S 8817C>T SKCM-US X 53565956 53565956 single base substitution G A synonymous_variant S3906S 11718C>T SKCM-US X 53565956 53565956 single base substitution G A synonymous_variant S728S 2184C>T SKCM-US X 53565956 53565956 single base substitution G A upstream_gene_variant SKCM-US X 53566728 53566728 single base substitution G A downstream_gene_variant SKCM-US X 53566728 53566728 single base substitution G A exon_variant SKCM-US X 53566728 53566728 single base substitution G A missense_variant P2874L 8621C>T SKCM-US X 53566728 53566728 single base substitution G A missense_variant P3841L 11522C>T SKCM-US X 53566728 53566728 single base substitution G A missense_variant P663L 1988C>T SKCM-US X 53566728 53566728 single base substitution G A upstream_gene_variant SKCM-US X 53566768 53566768 single base substitution C A downstream_gene_variant SKCM-US X 53566768 53566768 single base substitution C A exon_variant SKCM-US X 53566768 53566768 single base substitution C A missense_variant D2861Y 8581G>T SKCM-US X 53566768 53566768 single base substitution C A missense_variant D3828Y 11482G>T SKCM-US X 53566768 53566768 single base substitution C A missense_variant D650Y 1948G>T SKCM-US X 53566768 53566768 single base substitution C A upstream_gene_variant SKCM-US X 53573412 53573412 single base substitution G A exon_variant SKCM-US X 53573412 53573412 single base substitution G A missense_variant L2667F 7999C>T SKCM-US X 53573412 53573412 single base substitution G A missense_variant L3634F 10900C>T SKCM-US X 53573412 53573412 single base substitution G A missense_variant L471F 1411C>T SKCM-US X 53573412 53573412 single base substitution G A upstream_gene_variant SKCM-US X 53573714 53573714 single base substitution T C exon_variant SKCM-US X 53573714 53573714 single base substitution T C missense_variant K2603R 7808A>G SKCM-US X 53573714 53573714 single base substitution T C missense_variant K3570R 10709A>G SKCM-US X 53573714 53573714 single base substitution T C missense_variant K407R 1220A>G SKCM-US X 53573714 53573714 single base substitution T C upstream_gene_variant SKCM-US X 53574695 53574695 single base substitution G A exon_variant SKCM-US X 53574695 53574695 single base substitution G A synonymous_variant T2558T 7674C>T SKCM-US X 53574695 53574695 single base substitution G A synonymous_variant T3525T 10575C>T SKCM-US X 53574695 53574695 single base substitution G A synonymous_variant T362T 1086C>T SKCM-US X 53574695 53574695 single base substitution G A upstream_gene_variant SKCM-US X 53574783 53574785 deletion of <=200bp GTG - disruptive_inframe_deletion TT2528T SKCM-US X 53574783 53574785 deletion of <=200bp GTG - disruptive_inframe_deletion TT332T SKCM-US X 53574783 53574785 deletion of <=200bp GTG - disruptive_inframe_deletion TT3495T SKCM-US X 53574783 53574785 deletion of <=200bp GTG - exon_variant SKCM-US X 53574783 53574785 deletion of <=200bp GTG - upstream_gene_variant SKCM-US X 53574852 53574852 single base substitution T C exon_variant SKCM-US X 53574852 53574852 single base substitution T C missense_variant Q2506R 7517A>G SKCM-US X 53574852 53574852 single base substitution T C missense_variant Q310R 929A>G SKCM-US X 53574852 53574852 single base substitution T C missense_variant Q3473R 10418A>G SKCM-US X 53574852 53574852 single base substitution T C upstream_gene_variant SKCM-US X 53575230 53575230 single base substitution A T missense_variant F184Y 551T>A SKCM-US X 53575230 53575230 single base substitution A T missense_variant F2380Y 7139T>A SKCM-US X 53575230 53575230 single base substitution A T missense_variant F3347Y 10040T>A SKCM-US X 53575230 53575230 single base substitution A T upstream_gene_variant SKCM-US X 53576039 53576039 insertion of <=200bp - ACGC frameshift_variant S143CV? SKCM-US X 53576039 53576039 insertion of <=200bp - ACGC frameshift_variant S2339CV? SKCM-US X 53576039 53576039 insertion of <=200bp - ACGC frameshift_variant S3306CV? SKCM-US X 53576039 53576039 insertion of <=200bp - ACGC upstream_gene_variant SKCM-US X 53576162 53576162 single base substitution C T missense_variant E102K 304G>A SKCM-US X 53576162 53576162 single base substitution C T missense_variant E2298K 6892G>A SKCM-US X 53576162 53576162 single base substitution C T missense_variant E3265K 9793G>A SKCM-US X 53576162 53576162 single base substitution C T upstream_gene_variant SKCM-US X 53576271 53576271 single base substitution G A synonymous_variant S2261S 6783C>T SKCM-US X 53576271 53576271 single base substitution G A synonymous_variant S3228S 9684C>T SKCM-US X 53576271 53576271 single base substitution G A synonymous_variant S65S 195C>T SKCM-US X 53576271 53576271 single base substitution G A upstream_gene_variant SKCM-US X 53577633 53577633 single base substitution T C missense_variant H2194R 6581A>G SKCM-US X 53577633 53577633 single base substitution T C missense_variant H3161R 9482A>G SKCM-US X 53577633 53577633 single base substitution T C upstream_gene_variant SKCM-US X 53581619 53581619 single base substitution C T missense_variant M1856I 5568G>A SKCM-US X 53581619 53581619 single base substitution C T missense_variant M2823I 8469G>A SKCM-US X 53581758 53581758 single base substitution G A missense_variant P1810L 5429C>T SKCM-US X 53581758 53581758 single base substitution G A missense_variant P2777L 8330C>T SKCM-US X 53585694 53585694 single base substitution C T synonymous_variant R1727R 5181G>A SKCM-US X 53585694 53585694 single base substitution C T synonymous_variant R2694R 8082G>A SKCM-US X 53592178 53592178 single base substitution T C missense_variant N1277D 3829A>G SKCM-US X 53592178 53592178 single base substitution T C missense_variant N2244D 6730A>G SKCM-US X 53595718 53595718 single base substitution C T missense_variant R1247Q 3740G>A SKCM-US X 53595718 53595718 single base substitution C T missense_variant R2214Q 6641G>A SKCM-US X 53600725 53600725 single base substitution A G synonymous_variant S1132S 3396T>C SKCM-US X 53600725 53600725 single base substitution A G synonymous_variant S2099S 6297T>C SKCM-US X 53600921 53600921 single base substitution G A missense_variant S1067L 3200C>T SKCM-US X 53600921 53600921 single base substitution G A missense_variant S2034L 6101C>T SKCM-US X 53607976 53607976 single base substitution G A downstream_gene_variant SKCM-US X 53607976 53607976 single base substitution G A missense_variant S1844L 5531C>T SKCM-US X 53607976 53607976 single base substitution G A missense_variant S877L 2630C>T SKCM-US X 53610870 53610870 single base substitution G A downstream_gene_variant SKCM-US X 53610870 53610870 single base substitution G A missense_variant P1723L 5168C>T SKCM-US X 53610870 53610870 single base substitution G A missense_variant P756L 2267C>T SKCM-US X 53611302 53611302 single base substitution T C intron_variant SKCM-US X 53611302 53611302 single base substitution T C missense_variant N1669D 5005A>G SKCM-US X 53611302 53611302 single base substitution T C missense_variant N702D 2104A>G SKCM-US X 53612009 53612009 single base substitution C T missense_variant R1655Q 4964G>A SKCM-US X 53612009 53612009 single base substitution C T missense_variant R688Q 2063G>A SKCM-US X 53613787 53613787 single base substitution G A missense_variant P1566L 4697C>T SKCM-US X 53613787 53613787 single base substitution G A missense_variant P599L 1796C>T SKCM-US X 53616539 53616539 single base substitution G A missense_variant R1477C 4429C>T SKCM-US X 53616539 53616539 single base substitution G A missense_variant R510C 1528C>T SKCM-US X 53617393 53617393 single base substitution G A missense_variant P1388S 4162C>T SKCM-US X 53617393 53617393 single base substitution G A missense_variant P421S 1261C>T SKCM-US X 53617456 53617456 single base substitution G A missense_variant L1367F 4099C>T SKCM-US X 53617456 53617456 single base substitution G A missense_variant L400F 1198C>T SKCM-US X 53619423 53619423 single base substitution C T missense_variant D1303N 3907G>A SKCM-US X 53619423 53619423 single base substitution C T missense_variant D336N 1006G>A SKCM-US X 53620471 53620471 single base substitution G A synonymous_variant F1198F 3594C>T SKCM-US X 53620471 53620471 single base substitution G A synonymous_variant F231F 693C>T SKCM-US X 53621488 53621488 single base substitution G A synonymous_variant L1158L 3474C>T SKCM-US X 53621488 53621488 single base substitution G A synonymous_variant L191L 573C>T SKCM-US X 53622156 53622156 single base substitution G A missense_variant P1124L 3371C>T SKCM-US X 53622156 53622156 single base substitution G A missense_variant P157L 470C>T SKCM-US X 53630442 53630442 single base substitution G A synonymous_variant S921S 2763C>T SKCM-US X 53630442 53630442 single base substitution G A upstream_gene_variant SKCM-US X 53630443 53630443 single base substitution G A missense_variant S921F 2762C>T SKCM-US X 53630443 53630443 single base substitution G A upstream_gene_variant SKCM-US X 53631699 53631699 single base substitution G A missense_variant P865S 2593C>T SKCM-US X 53631699 53631699 single base substitution G A upstream_gene_variant SKCM-US X 53642793 53642793 single base substitution T G exon_variant SKCM-US X 53642793 53642793 single base substitution T G missense_variant D654A 1961A>C SKCM-US X 53642794 53642794 single base substitution C T missense_variant D654N 1960G>A SKCM-US X 53642794 53642794 single base substitution C T splice_region_variant SKCM-US X 53643934 53643934 single base substitution G A exon_variant SKCM-US X 53643934 53643934 single base substitution G A missense_variant L652F 1954C>T SKCM-US X 53654416 53654416 single base substitution C T downstream_gene_variant SKCM-US X 53654416 53654416 single base substitution C T synonymous_variant K478K 1434G>A SKCM-US X 53654416 53654416 single base substitution C T synonymous_variant K75K 225G>A SKCM-US X 53654416 53654416 single base substitution C T upstream_gene_variant SKCM-US X 53654425 53654425 single base substitution G A downstream_gene_variant SKCM-US X 53654425 53654425 single base substitution G A synonymous_variant I475I 1425C>T SKCM-US X 53654425 53654425 single base substitution G A synonymous_variant I72I 216C>T SKCM-US X 53654425 53654425 single base substitution G A upstream_gene_variant SKCM-US X 53654436 53654436 single base substitution G A downstream_gene_variant SKCM-US X 53654436 53654436 single base substitution G A missense_variant P472S 1414C>T SKCM-US X 53654436 53654436 single base substitution G A missense_variant P69S 205C>T SKCM-US X 53654436 53654436 single base substitution G A upstream_gene_variant SKCM-US X 53657952 53657952 single base substitution C T exon_variant SKCM-US X 53657952 53657952 single base substitution C T missense_variant G266D 797G>A SKCM-US X 53657952 53657952 single base substitution C T upstream_gene_variant SKCM-US X 53674318 53674318 single base substitution G A downstream_gene_variant SKCM-US X 53674318 53674318 single base substitution G A missense_variant S115F 344C>T STAD-US X 53562382 53562384 deletion of <=200bp CTT - downstream_gene_variant STAD-US X 53562382 53562384 deletion of <=200bp CTT - inframe_deletion K1026 STAD-US X 53562382 53562384 deletion of <=200bp CTT - inframe_deletion K3237 STAD-US X 53562382 53562384 deletion of <=200bp CTT - inframe_deletion K4204 STAD-US X 53562382 53562384 deletion of <=200bp CTT - upstream_gene_variant STAD-US X 53562434 53562434 single base substitution C T downstream_gene_variant STAD-US X 53562434 53562434 single base substitution C T missense_variant R1009H 3026G>A STAD-US X 53562434 53562434 single base substitution C T missense_variant R3220H 9659G>A STAD-US X 53562434 53562434 single base substitution C T missense_variant R4187H 12560G>A STAD-US X 53562434 53562434 single base substitution C T upstream_gene_variant STAD-US X 53563191 53563191 single base substitution C G downstream_gene_variant STAD-US X 53563191 53563191 single base substitution C G exon_variant STAD-US X 53563191 53563191 single base substitution C G missense_variant D3183H 9547G>C STAD-US X 53563191 53563191 single base substitution C G missense_variant D4150H 12448G>C STAD-US X 53563191 53563191 single base substitution C G missense_variant D972H 2914G>C STAD-US X 53563191 53563191 single base substitution C G upstream_gene_variant STAD-US X 53563521 53563521 single base substitution C T downstream_gene_variant STAD-US X 53563521 53563521 single base substitution C T exon_variant STAD-US X 53563521 53563521 single base substitution C T missense_variant R3115H 9344G>A STAD-US X 53563521 53563521 single base substitution C T missense_variant R4082H 12245G>A STAD-US X 53563521 53563521 single base substitution C T missense_variant R904H 2711G>A STAD-US X 53563521 53563521 single base substitution C T upstream_gene_variant STAD-US X 53564520 53564520 single base substitution C T downstream_gene_variant STAD-US X 53564520 53564520 single base substitution C T exon_variant STAD-US X 53564520 53564520 single base substitution C T missense_variant R3078Q 9233G>A STAD-US X 53564520 53564520 single base substitution C T missense_variant R4045Q 12134G>A STAD-US X 53564520 53564520 single base substitution C T missense_variant R867Q 2600G>A STAD-US X 53564520 53564520 single base substitution C T upstream_gene_variant STAD-US X 53566005 53566005 single base substitution T C downstream_gene_variant STAD-US X 53566005 53566005 single base substitution T C missense_variant H2923R 8768A>G STAD-US X 53566005 53566005 single base substitution T C missense_variant H3890R 11669A>G STAD-US X 53566005 53566005 single base substitution T C missense_variant H712R 2135A>G STAD-US X 53566005 53566005 single base substitution T C upstream_gene_variant STAD-US X 53569478 53569478 single base substitution G A downstream_gene_variant STAD-US X 53569478 53569478 single base substitution G A exon_variant STAD-US X 53569478 53569478 single base substitution G A missense_variant A2834V 8501C>T STAD-US X 53569478 53569478 single base substitution G A missense_variant A3801V 11402C>T STAD-US X 53569478 53569478 single base substitution G A missense_variant A623V 1868C>T STAD-US X 53569478 53569478 single base substitution G A upstream_gene_variant STAD-US X 53573484 53573484 single base substitution G A exon_variant STAD-US X 53573484 53573484 single base substitution G A missense_variant R2643W 7927C>T STAD-US X 53573484 53573484 single base substitution G A missense_variant R3610W 10828C>T STAD-US X 53573484 53573484 single base substitution G A missense_variant R447W 1339C>T STAD-US X 53573484 53573484 single base substitution G A upstream_gene_variant STAD-US X 53574690 53574690 single base substitution A G exon_variant STAD-US X 53574690 53574690 single base substitution A G missense_variant V2560A 7679T>C STAD-US X 53574690 53574690 single base substitution A G missense_variant V3527A 10580T>C STAD-US X 53574690 53574690 single base substitution A G missense_variant V364A 1091T>C STAD-US X 53574690 53574690 single base substitution A G upstream_gene_variant STAD-US X 53574768 53574768 single base substitution G A exon_variant STAD-US X 53574768 53574768 single base substitution G A missense_variant T2534M 7601C>T STAD-US X 53574768 53574768 single base substitution G A missense_variant T338M 1013C>T STAD-US X 53574768 53574768 single base substitution G A missense_variant T3501M 10502C>T STAD-US X 53574768 53574768 single base substitution G A upstream_gene_variant STAD-US X 53574996 53574996 single base substitution C T exon_variant STAD-US X 53574996 53574996 single base substitution C T missense_variant S2458N 7373G>A STAD-US X 53574996 53574996 single base substitution C T missense_variant S262N 785G>A STAD-US X 53574996 53574996 single base substitution C T missense_variant S3425N 10274G>A STAD-US X 53574996 53574996 single base substitution C T upstream_gene_variant STAD-US X 53575028 53575028 single base substitution G A synonymous_variant S2447S 7341C>T STAD-US X 53575028 53575028 single base substitution G A synonymous_variant S251S 753C>T STAD-US X 53575028 53575028 single base substitution G A synonymous_variant S3414S 10242C>T STAD-US X 53575028 53575028 single base substitution G A upstream_gene_variant STAD-US X 53575080 53575080 single base substitution T C missense_variant N234S 701A>G STAD-US X 53575080 53575080 single base substitution T C missense_variant N2430S 7289A>G STAD-US X 53575080 53575080 single base substitution T C missense_variant N3397S 10190A>G STAD-US X 53575080 53575080 single base substitution T C upstream_gene_variant STAD-US X 53575177 53575177 single base substitution G A missense_variant R202W 604C>T STAD-US X 53575177 53575177 single base substitution G A missense_variant R2398W 7192C>T STAD-US X 53575177 53575177 single base substitution G A missense_variant R3365W 10093C>T STAD-US X 53575177 53575177 single base substitution G A upstream_gene_variant STAD-US X 53576031 53576031 insertion of <=200bp - C frameshift_variant G145G? STAD-US X 53576031 53576031 insertion of <=200bp - C frameshift_variant G2341G? STAD-US X 53576031 53576031 insertion of <=200bp - C frameshift_variant G3308G? STAD-US X 53576031 53576031 insertion of <=200bp - C upstream_gene_variant STAD-US X 53576261 53576261 single base substitution G A missense_variant R2265C 6793C>T STAD-US X 53576261 53576261 single base substitution G A missense_variant R3232C 9694C>T STAD-US X 53576261 53576261 single base substitution G A missense_variant R69C 205C>T STAD-US X 53576261 53576261 single base substitution G A upstream_gene_variant STAD-US X 53579769 53579769 single base substitution G A synonymous_variant S1893S 5679C>T STAD-US X 53579769 53579769 single base substitution G A synonymous_variant S2860S 8580C>T STAD-US X 53579769 53579769 single base substitution G A upstream_gene_variant STAD-US X 53581651 53581651 single base substitution T G synonymous_variant R1846R 5536A>C STAD-US X 53581651 53581651 single base substitution T G synonymous_variant R2813R 8437A>C STAD-US X 53586338 53586338 single base substitution T C missense_variant Q1664R 4991A>G STAD-US X 53586338 53586338 single base substitution T C missense_variant Q2631R 7892A>G STAD-US X 53586416 53586416 single base substitution C T missense_variant R1638H 4913G>A STAD-US X 53586416 53586416 single base substitution C T missense_variant R2605H 7814G>A STAD-US X 53586422 53586422 single base substitution C T missense_variant R1636Q 4907G>A STAD-US X 53586422 53586422 single base substitution C T missense_variant R2603Q 7808G>A STAD-US X 53587255 53587255 single base substitution C T missense_variant G1577R 4729G>A STAD-US X 53587255 53587255 single base substitution C T missense_variant G2544R 7630G>A STAD-US X 53587313 53587313 single base substitution G A synonymous_variant D1557D 4671C>T STAD-US X 53587313 53587313 single base substitution G A synonymous_variant D2524D 7572C>T STAD-US X 53588851 53588851 single base substitution T C missense_variant D1491G 4472A>G STAD-US X 53588851 53588851 single base substitution T C missense_variant D2458G 7373A>G STAD-US X 53589102 53589102 single base substitution C T synonymous_variant E1469E 4407G>A STAD-US X 53589102 53589102 single base substitution C T synonymous_variant E2436E 7308G>A STAD-US X 53589856 53589856 single base substitution G A synonymous_variant D1413D 4239C>T STAD-US X 53589856 53589856 single base substitution G A synonymous_variant D2380D 7140C>T STAD-US X 53590731 53590731 single base substitution C T missense_variant G1394R 4180G>A STAD-US X 53590731 53590731 single base substitution C T missense_variant G2361R 7081G>A STAD-US X 53590779 53590779 single base substitution C T missense_variant E1378K 4132G>A STAD-US X 53590779 53590779 single base substitution C T missense_variant E2345K 7033G>A STAD-US X 53600835 53600835 single base substitution T C missense_variant K1096E 3286A>G STAD-US X 53600835 53600835 single base substitution T C missense_variant K2063E 6187A>G STAD-US X 53607904 53607904 single base substitution T C downstream_gene_variant STAD-US X 53607904 53607904 single base substitution T C missense_variant N1868S 5603A>G STAD-US X 53607904 53607904 single base substitution T C missense_variant N901S 2702A>G STAD-US X 53610583 53610583 single base substitution G A downstream_gene_variant STAD-US X 53610583 53610583 single base substitution G A synonymous_variant L1819L 5455C>T STAD-US X 53610583 53610583 single base substitution G A synonymous_variant L852L 2554C>T STAD-US X 53613488 53613488 single base substitution T C missense_variant T1596A 4786A>G STAD-US X 53613488 53613488 single base substitution T C missense_variant T629A 1885A>G STAD-US X 53622292 53622292 single base substitution C A missense_variant V1079F 3235G>T STAD-US X 53622292 53622292 single base substitution C A missense_variant V112F 334G>T STAD-US X 53630414 53630414 single base substitution G A synonymous_variant L931L 2791C>T STAD-US X 53630414 53630414 single base substitution G A upstream_gene_variant STAD-US X 53631667 53631667 single base substitution A C synonymous_variant A875A 2625T>G STAD-US X 53631667 53631667 single base substitution A C upstream_gene_variant STAD-US X 53631775 53631775 single base substitution T G missense_variant K839N 2517A>C STAD-US X 53631775 53631775 single base substitution T G upstream_gene_variant STAD-US X 53641546 53641546 single base substitution G A downstream_gene_variant STAD-US X 53641546 53641546 single base substitution G A missense_variant A737V 2210C>T STAD-US X 53643948 53643950 deletion of <=200bp CTC - disruptive_inframe_deletion RR646R STAD-US X 53643948 53643950 deletion of <=200bp CTC - exon_variant STAD-US X 53652155 53652155 single base substitution G A exon_variant STAD-US X 53652155 53652155 single base substitution G A synonymous_variant A196A 588C>T STAD-US X 53652155 53652155 single base substitution G A synonymous_variant A518A 1554C>T STAD-US X 53654765 53654765 single base substitution A G downstream_gene_variant STAD-US X 53654765 53654765 single base substitution A G synonymous_variant V33V 99T>C STAD-US X 53654765 53654765 single base substitution A G synonymous_variant V436V 1308T>C STAD-US X 53654765 53654765 single base substitution A G upstream_gene_variant STAD-US X 53655775 53655775 single base substitution C T downstream_gene_variant STAD-US X 53655775 53655775 single base substitution C T missense_variant D348N 1042G>A STAD-US X 53655775 53655775 single base substitution C T upstream_gene_variant STAD-US X 53655786 53655786 single base substitution C A downstream_gene_variant STAD-US X 53655786 53655786 single base substitution C A missense_variant S344I 1031G>T STAD-US X 53655786 53655786 single base substitution C A upstream_gene_variant STAD-US X 53657955 53657955 single base substitution T C exon_variant STAD-US X 53657955 53657955 single base substitution T C missense_variant H265R 794A>G STAD-US X 53657955 53657955 single base substitution T C upstream_gene_variant STAD-US X 53672407 53672407 single base substitution T C downstream_gene_variant STAD-US X 53672407 53672407 single base substitution T C synonymous_variant T120T 360A>G STAD-US X 53674333 53674333 single base substitution C T downstream_gene_variant STAD-US X 53674333 53674333 single base substitution C T missense_variant R110Q 329G>A THCA-US X 53575049 53575049 single base substitution G A synonymous_variant S2440S 7320C>T THCA-US X 53575049 53575049 single base substitution G A synonymous_variant S244S 732C>T THCA-US X 53575049 53575049 single base substitution G A synonymous_variant S3407S 10221C>T THCA-US X 53575049 53575049 single base substitution G A upstream_gene_variant THCA-US X 53654447 53654447 single base substitution C T downstream_gene_variant THCA-US X 53654447 53654447 single base substitution C T missense_variant R468Q 1403G>A THCA-US X 53654447 53654447 single base substitution C T missense_variant R65Q 194G>A THCA-US X 53654447 53654447 single base substitution C T upstream_gene_variant UCEC-US X 53560307 53560307 single base substitution G A downstream_gene_variant UCEC-US X 53560307 53560307 single base substitution G A missense_variant A1185V 3554C>T UCEC-US X 53560307 53560307 single base substitution G A missense_variant A3396V 10187C>T UCEC-US X 53560307 53560307 single base substitution G A missense_variant A4363V 13088C>T UCEC-US X 53561082 53561082 single base substitution G A downstream_gene_variant UCEC-US X 53561082 53561082 single base substitution G A exon_variant UCEC-US X 53561082 53561082 single base substitution G A missense_variant T1125I 3374C>T UCEC-US X 53561082 53561082 single base substitution G A missense_variant T3336I 10007C>T UCEC-US X 53561082 53561082 single base substitution G A missense_variant T4303I 12908C>T UCEC-US X 53561130 53561130 single base substitution G T downstream_gene_variant UCEC-US X 53561130 53561130 single base substitution G T exon_variant UCEC-US X 53561130 53561130 single base substitution G T missense_variant S1109Y 3326C>A UCEC-US X 53561130 53561130 single base substitution G T missense_variant S3320Y 9959C>A UCEC-US X 53561130 53561130 single base substitution G T missense_variant S4287Y 12860C>A UCEC-US X 53561525 53561525 single base substitution A G downstream_gene_variant UCEC-US X 53561525 53561525 single base substitution A G exon_variant UCEC-US X 53561525 53561525 single base substitution A G synonymous_variant D1083D 3249T>C UCEC-US X 53561525 53561525 single base substitution A G synonymous_variant D3294D 9882T>C UCEC-US X 53561525 53561525 single base substitution A G synonymous_variant D4261D 12783T>C UCEC-US X 53561531 53561531 single base substitution G A downstream_gene_variant UCEC-US X 53561531 53561531 single base substitution G A exon_variant UCEC-US X 53561531 53561531 single base substitution G A synonymous_variant I1081I 3243C>T UCEC-US X 53561531 53561531 single base substitution G A synonymous_variant I3292I 9876C>T UCEC-US X 53561531 53561531 single base substitution G A synonymous_variant I4259I 12777C>T UCEC-US X 53562406 53562406 single base substitution G T downstream_gene_variant UCEC-US X 53562406 53562406 single base substitution G T synonymous_variant I1018I 3054C>A UCEC-US X 53562406 53562406 single base substitution G T synonymous_variant I3229I 9687C>A UCEC-US X 53562406 53562406 single base substitution G T synonymous_variant I4196I 12588C>A UCEC-US X 53562406 53562406 single base substitution G T upstream_gene_variant UCEC-US X 53563196 53563196 single base substitution C A downstream_gene_variant UCEC-US X 53563196 53563196 single base substitution C A exon_variant UCEC-US X 53563196 53563196 single base substitution C A missense_variant S3181I 9542G>T UCEC-US X 53563196 53563196 single base substitution C A missense_variant S4148I 12443G>T UCEC-US X 53563196 53563196 single base substitution C A missense_variant S970I 2909G>T UCEC-US X 53563196 53563196 single base substitution C A upstream_gene_variant UCEC-US X 53563516 53563516 single base substitution A G downstream_gene_variant UCEC-US X 53563516 53563516 single base substitution A G exon_variant UCEC-US X 53563516 53563516 single base substitution A G missense_variant S3117P 9349T>C UCEC-US X 53563516 53563516 single base substitution A G missense_variant S4084P 12250T>C UCEC-US X 53563516 53563516 single base substitution A G missense_variant S906P 2716T>C UCEC-US X 53563516 53563516 single base substitution A G upstream_gene_variant UCEC-US X 53563539 53563539 single base substitution G T downstream_gene_variant UCEC-US X 53563539 53563539 single base substitution G T exon_variant UCEC-US X 53563539 53563539 single base substitution G T missense_variant P3109H 9326C>A UCEC-US X 53563539 53563539 single base substitution G T missense_variant P4076H 12227C>A UCEC-US X 53563539 53563539 single base substitution G T missense_variant P898H 2693C>A UCEC-US X 53563539 53563539 single base substitution G T upstream_gene_variant UCEC-US X 53563593 53563593 single base substitution G A downstream_gene_variant UCEC-US X 53563593 53563593 single base substitution G A exon_variant UCEC-US X 53563593 53563593 single base substitution G A missense_variant A3091V 9272C>T UCEC-US X 53563593 53563593 single base substitution G A missense_variant A4058V 12173C>T UCEC-US X 53563593 53563593 single base substitution G A missense_variant A880V 2639C>T UCEC-US X 53563593 53563593 single base substitution G A upstream_gene_variant UCEC-US X 53564536 53564536 single base substitution C A downstream_gene_variant UCEC-US X 53564536 53564536 single base substitution C A exon_variant UCEC-US X 53564536 53564536 single base substitution C A stop_gained E3073* 9217G>T UCEC-US X 53564536 53564536 single base substitution C A stop_gained E4040* 12118G>T UCEC-US X 53564536 53564536 single base substitution C A stop_gained E862* 2584G>T UCEC-US X 53564536 53564536 single base substitution C A upstream_gene_variant UCEC-US X 53564636 53564636 single base substitution C A downstream_gene_variant UCEC-US X 53564636 53564636 single base substitution C A exon_variant UCEC-US X 53564636 53564636 single base substitution C A missense_variant E3039D 9117G>T UCEC-US X 53564636 53564636 single base substitution C A missense_variant E4006D 12018G>T UCEC-US X 53564636 53564636 single base substitution C A missense_variant E828D 2484G>T UCEC-US X 53564636 53564636 single base substitution C A upstream_gene_variant UCEC-US X 53565301 53565301 single base substitution C T downstream_gene_variant UCEC-US X 53565301 53565301 single base substitution C T exon_variant UCEC-US X 53565301 53565301 single base substitution C T missense_variant R3031H 9092G>A UCEC-US X 53565301 53565301 single base substitution C T missense_variant R3998H 11993G>A UCEC-US X 53565301 53565301 single base substitution C T missense_variant R820H 2459G>A UCEC-US X 53565301 53565301 single base substitution C T upstream_gene_variant UCEC-US X 53565352 53565352 single base substitution G T downstream_gene_variant UCEC-US X 53565352 53565352 single base substitution G T exon_variant UCEC-US X 53565352 53565352 single base substitution G T missense_variant P3014H 9041C>A UCEC-US X 53565352 53565352 single base substitution G T missense_variant P3981H 11942C>A UCEC-US X 53565352 53565352 single base substitution G T missense_variant P803H 2408C>A UCEC-US X 53565352 53565352 single base substitution G T upstream_gene_variant UCEC-US X 53565805 53565805 single base substitution G A downstream_gene_variant UCEC-US X 53565805 53565805 single base substitution G A missense_variant R2990C 8968C>T UCEC-US X 53565805 53565805 single base substitution G A missense_variant R3957C 11869C>T UCEC-US X 53565805 53565805 single base substitution G A missense_variant R779C 2335C>T UCEC-US X 53565805 53565805 single base substitution G A upstream_gene_variant UCEC-US X 53565906 53565906 single base substitution A G downstream_gene_variant UCEC-US X 53565906 53565906 single base substitution A G missense_variant L2956S 8867T>C UCEC-US X 53565906 53565906 single base substitution A G missense_variant L3923S 11768T>C UCEC-US X 53565906 53565906 single base substitution A G missense_variant L745S 2234T>C UCEC-US X 53565906 53565906 single base substitution A G upstream_gene_variant UCEC-US X 53566025 53566025 single base substitution G A downstream_gene_variant UCEC-US X 53566025 53566025 single base substitution G A synonymous_variant V2916V 8748C>T UCEC-US X 53566025 53566025 single base substitution G A synonymous_variant V3883V 11649C>T UCEC-US X 53566025 53566025 single base substitution G A synonymous_variant V705V 2115C>T UCEC-US X 53566025 53566025 single base substitution G A upstream_gene_variant UCEC-US X 53566739 53566739 single base substitution C A downstream_gene_variant UCEC-US X 53566739 53566739 single base substitution C A exon_variant UCEC-US X 53566739 53566739 single base substitution C A missense_variant K2870N 8610G>T UCEC-US X 53566739 53566739 single base substitution C A missense_variant K3837N 11511G>T UCEC-US X 53566739 53566739 single base substitution C A missense_variant K659N 1977G>T UCEC-US X 53566739 53566739 single base substitution C A upstream_gene_variant UCEC-US X 53569441 53569441 single base substitution G T downstream_gene_variant UCEC-US X 53569441 53569441 single base substitution G T exon_variant UCEC-US X 53569441 53569441 single base substitution G T missense_variant D2846E 8538C>A UCEC-US X 53569441 53569441 single base substitution G T missense_variant D3813E 11439C>A UCEC-US X 53569441 53569441 single base substitution G T missense_variant D635E 1905C>A UCEC-US X 53569441 53569441 single base substitution G T upstream_gene_variant UCEC-US X 53569498 53569498 single base substitution C T downstream_gene_variant UCEC-US X 53569498 53569498 single base substitution C T exon_variant UCEC-US X 53569498 53569498 single base substitution C T splice_region_variant UCEC-US X 53569498 53569498 single base substitution C T upstream_gene_variant UCEC-US X 53571546 53571546 single base substitution C A exon_variant UCEC-US X 53571546 53571546 single base substitution C A intron_variant UCEC-US X 53571546 53571546 single base substitution C A missense_variant K2775N 8325G>T UCEC-US X 53571546 53571546 single base substitution C A missense_variant K3742N 11226G>T UCEC-US X 53571546 53571546 single base substitution C A missense_variant K579N 1737G>T UCEC-US X 53571546 53571546 single base substitution C A upstream_gene_variant UCEC-US X 53571562 53571562 single base substitution G A exon_variant UCEC-US X 53571562 53571562 single base substitution G A intron_variant UCEC-US X 53571562 53571562 single base substitution G A missense_variant T2770M 8309C>T UCEC-US X 53571562 53571562 single base substitution G A missense_variant T3737M 11210C>T UCEC-US X 53571562 53571562 single base substitution G A missense_variant T574M 1721C>T UCEC-US X 53571562 53571562 single base substitution G A upstream_gene_variant UCEC-US X 53571575 53571575 single base substitution G T exon_variant UCEC-US X 53571575 53571575 single base substitution G T intron_variant UCEC-US X 53571575 53571575 single base substitution G T missense_variant L2766I 8296C>A UCEC-US X 53571575 53571575 single base substitution G T missense_variant L3733I 11197C>A UCEC-US X 53571575 53571575 single base substitution G T missense_variant L570I 1708C>A UCEC-US X 53571575 53571575 single base substitution G T upstream_gene_variant UCEC-US X 53571677 53571677 single base substitution G A exon_variant UCEC-US X 53571677 53571677 single base substitution G A intron_variant UCEC-US X 53571677 53571677 single base substitution G A missense_variant P2732S 8194C>T UCEC-US X 53571677 53571677 single base substitution G A missense_variant P3699S 11095C>T UCEC-US X 53571677 53571677 single base substitution G A missense_variant P536S 1606C>T UCEC-US X 53571677 53571677 single base substitution G A upstream_gene_variant UCEC-US X 53573451 53573451 single base substitution T C exon_variant UCEC-US X 53573451 53573451 single base substitution T C missense_variant K2654E 7960A>G UCEC-US X 53573451 53573451 single base substitution T C missense_variant K3621E 10861A>G UCEC-US X 53573451 53573451 single base substitution T C missense_variant K458E 1372A>G UCEC-US X 53573451 53573451 single base substitution T C upstream_gene_variant UCEC-US X 53573707 53573707 single base substitution C T exon_variant UCEC-US X 53573707 53573707 single base substitution C T synonymous_variant V2605V 7815G>A UCEC-US X 53573707 53573707 single base substitution C T synonymous_variant V3572V 10716G>A UCEC-US X 53573707 53573707 single base substitution C T synonymous_variant V409V 1227G>A UCEC-US X 53573707 53573707 single base substitution C T upstream_gene_variant UCEC-US X 53574656 53574656 single base substitution C T exon_variant UCEC-US X 53574656 53574656 single base substitution C T synonymous_variant T2571T 7713G>A UCEC-US X 53574656 53574656 single base substitution C T synonymous_variant T3538T 10614G>A UCEC-US X 53574656 53574656 single base substitution C T synonymous_variant T375T 1125G>A UCEC-US X 53574656 53574656 single base substitution C T upstream_gene_variant UCEC-US X 53574732 53574732 single base substitution G A exon_variant UCEC-US X 53574732 53574732 single base substitution G A missense_variant S2546F 7637C>T UCEC-US X 53574732 53574732 single base substitution G A missense_variant S350F 1049C>T UCEC-US X 53574732 53574732 single base substitution G A missense_variant S3513F 10538C>T UCEC-US X 53574732 53574732 single base substitution G A upstream_gene_variant UCEC-US X 53574861 53574861 single base substitution G A exon_variant UCEC-US X 53574861 53574861 single base substitution G A missense_variant S2503L 7508C>T UCEC-US X 53574861 53574861 single base substitution G A missense_variant S307L 920C>T UCEC-US X 53574861 53574861 single base substitution G A missense_variant S3470L 10409C>T UCEC-US X 53574861 53574861 single base substitution G A upstream_gene_variant UCEC-US X 53574888 53574888 single base substitution G A exon_variant UCEC-US X 53574888 53574888 single base substitution G A missense_variant S2494L 7481C>T UCEC-US X 53574888 53574888 single base substitution G A missense_variant S298L 893C>T UCEC-US X 53574888 53574888 single base substitution G A missense_variant S3461L 10382C>T UCEC-US X 53574888 53574888 single base substitution G A upstream_gene_variant UCEC-US X 53575022 53575022 single base substitution G A synonymous_variant G2449G 7347C>T UCEC-US X 53575022 53575022 single base substitution G A synonymous_variant G253G 759C>T UCEC-US X 53575022 53575022 single base substitution G A synonymous_variant G3416G 10248C>T UCEC-US X 53575022 53575022 single base substitution G A upstream_gene_variant UCEC-US X 53575177 53575177 single base substitution G A missense_variant R202W 604C>T UCEC-US X 53575177 53575177 single base substitution G A missense_variant R2398W 7192C>T UCEC-US X 53575177 53575177 single base substitution G A missense_variant R3365W 10093C>T UCEC-US X 53575177 53575177 single base substitution G A upstream_gene_variant UCEC-US X 53576064 53576064 single base substitution C A missense_variant R134S 402G>T UCEC-US X 53576064 53576064 single base substitution C A missense_variant R2330S 6990G>T UCEC-US X 53576064 53576064 single base substitution C A missense_variant R3297S 9891G>T UCEC-US X 53576064 53576064 single base substitution C A upstream_gene_variant UCEC-US X 53576321 53576321 single base substitution G T missense_variant L2245I 6733C>A UCEC-US X 53576321 53576321 single base substitution G T missense_variant L3212I 9634C>A UCEC-US X 53576321 53576321 single base substitution G T missense_variant L49I 145C>A UCEC-US X 53576321 53576321 single base substitution G T upstream_gene_variant UCEC-US X 53576406 53576406 single base substitution G A synonymous_variant H20H 60C>T UCEC-US X 53576406 53576406 single base substitution G A synonymous_variant H2216H 6648C>T UCEC-US X 53576406 53576406 single base substitution G A synonymous_variant H3183H 9549C>T UCEC-US X 53576406 53576406 single base substitution G A upstream_gene_variant UCEC-US X 53576423 53576423 single base substitution G A missense_variant R15W 43C>T UCEC-US X 53576423 53576423 single base substitution G A missense_variant R2211W 6631C>T UCEC-US X 53576423 53576423 single base substitution G A missense_variant R3178W 9532C>T UCEC-US X 53576423 53576423 single base substitution G A upstream_gene_variant UCEC-US X 53576425 53576425 single base substitution C T missense_variant G14E 41G>A UCEC-US X 53576425 53576425 single base substitution C T missense_variant G2210E 6629G>A UCEC-US X 53576425 53576425 single base substitution C T missense_variant G3177E 9530G>A UCEC-US X 53576425 53576425 single base substitution C T upstream_gene_variant UCEC-US X 53577915 53577915 single base substitution C T missense_variant R2144H 6431G>A UCEC-US X 53577915 53577915 single base substitution C T missense_variant R3111H 9332G>A UCEC-US X 53577915 53577915 single base substitution C T upstream_gene_variant UCEC-US X 53578035 53578035 single base substitution C T missense_variant R2104H 6311G>A UCEC-US X 53578035 53578035 single base substitution C T missense_variant R3071H 9212G>A UCEC-US X 53578035 53578035 single base substitution C T upstream_gene_variant UCEC-US X 53579313 53579313 single base substitution G A missense_variant P1980L 5939C>T UCEC-US X 53579313 53579313 single base substitution G A missense_variant P2947L 8840C>T UCEC-US X 53579313 53579313 single base substitution G A upstream_gene_variant UCEC-US X 53579824 53579824 single base substitution G T missense_variant S1875Y 5624C>A UCEC-US X 53579824 53579824 single base substitution G T missense_variant S2842Y 8525C>A UCEC-US X 53579824 53579824 single base substitution G T upstream_gene_variant UCEC-US X 53579836 53579836 single base substitution C T missense_variant R1871K 5612G>A UCEC-US X 53579836 53579836 single base substitution C T missense_variant R2838K 8513G>A UCEC-US X 53579836 53579836 single base substitution C T upstream_gene_variant UCEC-US X 53581811 53581811 single base substitution C A missense_variant K1792N 5376G>T UCEC-US X 53581811 53581811 single base substitution C A missense_variant K2759N 8277G>T UCEC-US X 53585660 53585660 single base substitution C T missense_variant D1739N 5215G>A UCEC-US X 53585660 53585660 single base substitution C T missense_variant D2706N 8116G>A UCEC-US X 53585965 53585965 single base substitution G A missense_variant L1691F 5071C>T UCEC-US X 53585965 53585965 single base substitution G A missense_variant L2658F 7972C>T UCEC-US X 53585965 53585965 single base substitution G T missense_variant L1691I 5071C>A UCEC-US X 53585965 53585965 single base substitution G T missense_variant L2658I 7972C>A UCEC-US X 53588799 53588799 single base substitution G A synonymous_variant N1508N 4524C>T UCEC-US X 53588799 53588799 single base substitution G A synonymous_variant N2475N 7425C>T UCEC-US X 53588830 53588830 single base substitution A G missense_variant M1498T 4493T>C UCEC-US X 53588830 53588830 single base substitution A G missense_variant M2465T 7394T>C UCEC-US X 53590732 53590732 single base substitution G A synonymous_variant G1393G 4179C>T UCEC-US X 53590732 53590732 single base substitution G A synonymous_variant G2360G 7080C>T UCEC-US X 53591584 53591584 single base substitution G T stop_gained S1360* 4079C>A UCEC-US X 53591584 53591584 single base substitution G T stop_gained S2327* 6980C>A UCEC-US X 53591641 53591641 single base substitution A G missense_variant V1341A 4022T>C UCEC-US X 53591641 53591641 single base substitution A G missense_variant V2308A 6923T>C UCEC-US X 53591681 53591681 single base substitution C T missense_variant E1328K 3982G>A UCEC-US X 53591681 53591681 single base substitution C T missense_variant E2295K 6883G>A UCEC-US X 53595719 53595719 single base substitution G A missense_variant R1247W 3739C>T UCEC-US X 53595719 53595719 single base substitution G A missense_variant R2214W 6640C>T UCEC-US X 53595723 53595723 single base substitution G T synonymous_variant I1245I 3735C>A UCEC-US X 53595723 53595723 single base substitution G T synonymous_variant I2212I 6636C>A UCEC-US X 53595725 53595725 single base substitution T C missense_variant I1245V 3733A>G UCEC-US X 53595725 53595725 single base substitution T C missense_variant I2212V 6634A>G UCEC-US X 53595736 53595736 single base substitution C T missense_variant G1241D 3722G>A UCEC-US X 53595736 53595736 single base substitution C T missense_variant G2208D 6623G>A UCEC-US X 53596580 53596580 single base substitution C T missense_variant A1207T 3619G>A UCEC-US X 53596580 53596580 single base substitution C T missense_variant A2174T 6520G>A UCEC-US X 53596641 53596641 single base substitution C A synonymous_variant V1186V 3558G>T UCEC-US X 53596641 53596641 single base substitution C A synonymous_variant V2153V 6459G>T UCEC-US X 53596773 53596773 single base substitution T C synonymous_variant L1142L 3426A>G UCEC-US X 53596773 53596773 single base substitution T C synonymous_variant L2109L 6327A>G UCEC-US X 53600893 53600893 single base substitution C A missense_variant K1076N 3228G>T UCEC-US X 53600893 53600893 single base substitution C A missense_variant K2043N 6129G>T UCEC-US X 53602139 53602139 single base substitution C T missense_variant A1058T 3172G>A UCEC-US X 53602139 53602139 single base substitution C T missense_variant A2025T 6073G>A UCEC-US X 53607796 53607796 single base substitution C T downstream_gene_variant UCEC-US X 53607796 53607796 single base substitution C T missense_variant G1904E 5711G>A UCEC-US X 53607796 53607796 single base substitution C T missense_variant G937E 2810G>A UCEC-US X 53607797 53607797 single base substitution C A downstream_gene_variant UCEC-US X 53607797 53607797 single base substitution C A stop_gained G1904* 5710G>T UCEC-US X 53607797 53607797 single base substitution C A stop_gained G937* 2809G>T UCEC-US X 53607838 53607838 single base substitution T C downstream_gene_variant UCEC-US X 53607838 53607838 single base substitution T C missense_variant N1890S 5669A>G UCEC-US X 53607838 53607838 single base substitution T C missense_variant N923S 2768A>G UCEC-US X 53610571 53610571 single base substitution G A downstream_gene_variant UCEC-US X 53610571 53610571 single base substitution G A missense_variant L1823F 5467C>T UCEC-US X 53610571 53610571 single base substitution G A missense_variant L856F 2566C>T UCEC-US X 53610699 53610699 single base substitution C T downstream_gene_variant UCEC-US X 53610699 53610699 single base substitution C T missense_variant R1780H 5339G>A UCEC-US X 53610699 53610699 single base substitution C T missense_variant R813H 2438G>A UCEC-US X 53610721 53610721 single base substitution C A downstream_gene_variant UCEC-US X 53610721 53610721 single base substitution C A missense_variant D1773Y 5317G>T UCEC-US X 53610721 53610721 single base substitution C A missense_variant D806Y 2416G>T UCEC-US X 53610781 53610781 single base substitution C A downstream_gene_variant UCEC-US X 53610781 53610781 single base substitution C A missense_variant D1753Y 5257G>T UCEC-US X 53610781 53610781 single base substitution C A missense_variant D786Y 2356G>T UCEC-US X 53610792 53610792 single base substitution C A downstream_gene_variant UCEC-US X 53610792 53610792 single base substitution C A missense_variant G1749V 5246G>T UCEC-US X 53610792 53610792 single base substitution C A missense_variant G782V 2345G>T UCEC-US X 53611182 53611182 single base substitution C A 3_prime_UTR_variant UCEC-US X 53611182 53611182 single base substitution C A stop_gained E1709* 5125G>T UCEC-US X 53611182 53611182 single base substitution C A stop_gained E742* 2224G>T UCEC-US X 53613850 53613850 single base substitution G A missense_variant A1545V 4634C>T UCEC-US X 53613850 53613850 single base substitution G A missense_variant A578V 1733C>T UCEC-US X 53615346 53615346 single base substitution A C missense_variant F1537C 4610T>G UCEC-US X 53615346 53615346 single base substitution A C missense_variant F570C 1709T>G UCEC-US X 53615366 53615366 single base substitution G T synonymous_variant I1530I 4590C>A UCEC-US X 53615366 53615366 single base substitution G T synonymous_variant I563I 1689C>A UCEC-US X 53615460 53615460 single base substitution G T missense_variant A1499D 4496C>A UCEC-US X 53615460 53615460 single base substitution G T missense_variant A532D 1595C>A UCEC-US X 53616665 53616665 single base substitution C A stop_gained E1435* 4303G>T UCEC-US X 53616665 53616665 single base substitution C A stop_gained E468* 1402G>T UCEC-US X 53616678 53616678 single base substitution C T synonymous_variant P1430P 4290G>A UCEC-US X 53616678 53616678 single base substitution C T synonymous_variant P463P 1389G>A UCEC-US X 53618076 53618076 single base substitution C A missense_variant D1327Y 3979G>T UCEC-US X 53618076 53618076 single base substitution C A missense_variant D360Y 1078G>T UCEC-US X 53620411 53620411 single base substitution A G synonymous_variant S1218S 3654T>C UCEC-US X 53620411 53620411 single base substitution A G synonymous_variant S251S 753T>C UCEC-US X 53620424 53620424 single base substitution G A missense_variant T1214M 3641C>T UCEC-US X 53620424 53620424 single base substitution G A missense_variant T247M 740C>T UCEC-US X 53627121 53627121 single base substitution T C synonymous_variant P1040P 3120A>G UCEC-US X 53627121 53627121 single base substitution T C synonymous_variant P73P 219A>G UCEC-US X 53627127 53627127 single base substitution G A synonymous_variant I1038I 3114C>T UCEC-US X 53627127 53627127 single base substitution G A synonymous_variant I71I 213C>T UCEC-US X 53627240 53627240 single base substitution T C missense_variant M1001V 3001A>G UCEC-US X 53627240 53627240 single base substitution T C missense_variant M34V 100A>G UCEC-US X 53629526 53629526 single base substitution T C intron_variant UCEC-US X 53629526 53629526 single base substitution T C splice_region_variant UCEC-US X 53630408 53630408 single base substitution C T missense_variant V933I 2797G>A UCEC-US X 53630408 53630408 single base substitution C T upstream_gene_variant UCEC-US X 53634621 53634621 single base substitution C A missense_variant D787Y 2359G>T UCEC-US X 53634621 53634621 single base substitution C A upstream_gene_variant UCEC-US X 53634626 53634626 single base substitution G A missense_variant T785I 2354C>T UCEC-US X 53634626 53634626 single base substitution G A upstream_gene_variant UCEC-US X 53634632 53634632 single base substitution T C missense_variant N783S 2348A>G UCEC-US X 53634632 53634632 single base substitution T C upstream_gene_variant UCEC-US X 53641672 53641672 single base substitution G T downstream_gene_variant UCEC-US X 53641672 53641672 single base substitution G T missense_variant P695H 2084C>A UCEC-US X 53644087 53644087 single base substitution G T exon_variant UCEC-US X 53644087 53644087 single base substitution G T missense_variant L601I 1801C>A UCEC-US X 53644303 53644303 single base substitution C A missense_variant D593Y 1777G>T UCEC-US X 53644303 53644303 single base substitution C A splice_region_variant UCEC-US X 53651562 53651562 single base substitution G T downstream_gene_variant UCEC-US X 53651562 53651562 single base substitution G T exon_variant UCEC-US X 53651562 53651562 single base substitution G T missense_variant L556I 1666C>A UCEC-US X 53652152 53652152 single base substitution G A exon_variant UCEC-US X 53652152 53652152 single base substitution G A synonymous_variant I197I 591C>T UCEC-US X 53652152 53652152 single base substitution G A synonymous_variant I519I 1557C>T UCEC-US X 53654453 53654453 single base substitution A G downstream_gene_variant UCEC-US X 53654453 53654453 single base substitution A G missense_variant L466S 1397T>C UCEC-US X 53654453 53654453 single base substitution A G missense_variant L63S 188T>C UCEC-US X 53654453 53654453 single base substitution A G upstream_gene_variant UCEC-US X 53655837 53655837 single base substitution G T downstream_gene_variant UCEC-US X 53655837 53655837 single base substitution G T missense_variant S327Y 980C>A UCEC-US X 53655837 53655837 single base substitution G T upstream_gene_variant UCEC-US X 53672376 53672376 single base substitution C T downstream_gene_variant UCEC-US X 53672376 53672376 single base substitution C T missense_variant V131M 391G>A UCEC-US X 53674313 53674313 single base substitution C A downstream_gene_variant UCEC-US X 53674313 53674313 single base substitution C A stop_gained E117* 349G>T UCEC-US X 53674385 53674385 single base substitution G A missense_variant L93F 277C>T UCEC-US X 53674385 53674385 single base substitution G A synonymous_variant ?93 UCEC-US X 53674407 53674407 single base substitution T G missense_variant E85D 255A>C UCEC-US X 53675182 53675182 single base substitution C T synonymous_variant Q39Q 117G>A UCEC-US X 53681048 53681048 single base substitution T G missense_variant K2Q 4A>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-24-2289-01 COSM117000 c.6618G>T p.Q2206H Substitution - Missense 23:53564574-53564574 - TCGA-B5-A0JY-01 COSM1123085 c.11869C>T p.R3957C Substitution - Missense 23:53538844-53538844 - TARGET-30-PARHUX COSM1285457 c.8200G>T p.A2734S Substitution - Missense 23:53552858-53552858 - TCGA-E2-A1II-01 COSM1491087 c.12212T>G p.F4071C Substitution - Missense 23:53535491-53535491 - TCGA-10-0926-01 COSM71121 c.10790T>A p.L3597Q Substitution - Missense 23:53544691-53544691 - 587234 COSM1210176 c.7396C>T p.R2466W Substitution - Missense 23:53559462-53559462 - CSCC-44-T COSM4451377 c.11905A>G p.I3969V Substitution - Missense 23:53538428-53538428 - PD5925a COSM5788349 c.11983G>C p.D3995H Substitution - Missense 23:53538350-53538350 - PD6637a COSM3719911 c.7060G>T p.E2354* Substitution - Nonsense 23:53563791-53563791 - PCA78-2 COSM5415755 c.3362A>G p.N1121S Substitution - Missense 23:53592597-53592597 - ESCC-D20 COSM5046019 c.9144G>T p.Q3048H Substitution - Missense 23:53551142-53551142 - PCSI_0090_Pa_X COSM3379655 c.4615-2A>G p.? Unknown 23:53586911-53586911 - 215 COSM4424614 c.818G>A p.R273Q Substitution - Missense 23:53630979-53630979 - CHC1211T COSM4955001 c.9326G>T p.R3109L Substitution - Missense 23:53549338-53549338 - TCGA-BS-A0UV-01 COSM1123122 c.9763C>T p.R3255W Substitution - Missense 23:53548216-53548216 - TCGA-AP-A059-01 COSM1123110 c.10386G>A p.V3462V Substitution - coding silent 23:53546746-53546746 - TCGA-BS-A0UF-01 COSM1123176 c.6459G>T p.V2153V Substitution - coding silent 23:53569681-53569681 - TCGA-BR-8680-01 COSM4110151 c.10580T>C p.V3527A Substitution - Missense 23:53547729-53547729 - J33_T COSM3965370 c.10254G>A p.E3418E Substitution - coding silent 23:53548055-53548055 - 19M COSM5578726 c.2885C>T p.S962F Substitution - Missense 23:53602650-53602650 - TCGA-FP-8631-01 COSM4110159 c.8580C>T p.S2860S Substitution - coding silent 23:53552808-53552808 - PTC-14C COSM4156906 c.7117G>T p.G2373* Substitution - Nonsense 23:53562918-53562918 - Gp2D COSM2968243 c.12610delC p.L4204fs*4 Deletion - Frameshift 23:53534089-53534089 - 3N24-VS-3T24 COSM4979872 c.5603C>G p.S1868* Substitution - Nonsense 23:53575659-53575659 - OSCC-GB_01360111 COSM5955647 c.12103G>A p.D4035N Substitution - Missense 23:53536245-53536245 - TCGA-A8-A0A6-01 COSM3845057 c.6449T>G p.V2150G Substitution - Missense 23:53569691-53569691 - HT115 COSM1468621 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - TCGA-B5-A11H-01 COSM1123063 c.12783T>C p.D4261D Substitution - coding silent 23:53534564-53534564 - RK177_C01 COSM1636571 c.8887A>T p.S2963C Substitution - Missense 23:53551475-53551475 - CHC1715T COSM4789410 c.2881G>T p.A961S Substitution - Missense 23:53595275-53595275 - CSCC-44-T COSM4564011 c.11906_11907TC>AT p.I3969N Substitution - Missense 23:53538426-53538427 - TCGA-ER-A19M-06 COSM3562371 c.9354C>T p.S3118S Substitution - coding silent 23:53549310-53549310 - TCGA-29-1691-01 COSM1331792 c.3337T>C p.L1113L Substitution - coding silent 23:53595230-53595230 - RK177_C01 COSM1636572 c.8557A>T p.S2853C Substitution - Missense 23:53551475-53551475 - TCGA-D8-A1XK-01 COSM3845070 c.1116T>C p.D372D Substitution - coding silent 23:53628619-53628619 - PD6417a COSM5800352 c.9916G>A p.G3306S Substitution - Missense 23:53548063-53548063 - OSCC-GB_00290111 COSM3713965 c.7205-1G>C p.? Unknown 23:53562245-53562245 - TCGA-B5-A11H-01 COSM1123064 c.12453T>C p.D4151D Substitution - coding silent 23:53534564-53534564 - PAPLDL COSM5004429 c.3422G>A p.C1141Y Substitution - Missense 23:53592537-53592537 - S02237 COSM5676669 c.11206C>A p.L3736M Substitution - Missense 23:53539753-53539753 - TCGA-BH-A0BZ-01 COSM457753 c.3747T>A p.D1249E Substitution - Missense 23:53590437-53590437 - TCGA-AC-A23H-01 COSM3845067 c.2013C>T p.P671P Substitution - coding silent 23:53615780-53615780 - PAPNNX COSM2968492 c.5564G>A p.R1855Q Substitution - Missense 23:53575698-53575698 - EGC15 COSM4110150 c.10498C>T p.R3500W Substitution - Missense 23:53546523-53546523 - PCSI_0066_Pa_X COSM3379654 c.4371A>G p.E1457E Substitution - coding silent 23:53586532-53586532 - TCGA-34-5232-01 COSM756897 c.4692G>T p.E1564D Substitution - Missense 23:53584244-53584244 - LUAD-B02216 COSM356328 c.797G>C p.G266A Substitution - Missense 23:53631000-53631000 - TCGA-BH-A18P-01 COSM457755 c.1847G>T p.R616L Substitution - Missense 23:53617080-53617080 - TCGA-32-2495-01 COSM3406478 c.11205C>T p.D3735D Substitution - coding silent 23:53544606-53544606 - TCGA-D1-A103-01 COSM1123079 c.12018G>T p.E4006D Substitution - Missense 23:53537675-53537675 - SJLGG037 COSM1716226 c.6624G>A p.E2208E Substitution - coding silent 23:53563816-53563816 - CSCC-31-T COSM4508347 c.7720C>T p.P2574S Substitution - Missense 23:53560204-53560204 - I2L-P19Tb-Tumor-Organoid COSM5367075 c.12006C>T p.R4002R Substitution - coding silent 23:53537687-53537687 - TCGA-D7-A4YV-01 COSM4110187 c.2625T>G p.A875A Substitution - coding silent 23:53604706-53604706 - S01563 COSM311891 c.6307G>A p.A2103T Substitution - Missense 23:53565229-53565229 - HCT-15 COSM1682637 c.9646G>A p.A3216T Substitution - Missense 23:53549348-53549348 - TCGA-D1-A16X-01 COSM1123058 c.12860C>T p.A4287V Substitution - Missense 23:53533346-53533346 - TCGA-B5-A11E-01 COSM1123062 c.12530C>A p.S4177Y Substitution - Missense 23:53534169-53534169 - PD6417a COSM5800351 c.10246G>A p.G3416S Substitution - Missense 23:53548063-53548063 - CSCC-18-T COSM4513700 c.9150C>T p.S3050S Substitution - coding silent 23:53550674-53550674 - PT47 COSM5930393 c.11633-7A>G p.? Unknown 23:53539087-53539087 - TCGA-60-2698-01 COSM756907 c.7811C>G p.S2604* Substitution - Nonsense 23:53557411-53557411 - TCGA-AM-5820-01 COSM2968623 c.792C>A p.A264A Substitution - coding silent 23:53631005-53631005 - HCC2998 COSM1682628 c.10966C>T p.R3656W Substitution - Missense 23:53543924-53543924 - TCGA-B0-4713-01 COSM3364164 c.9034C>A p.P3012T Substitution - Missense 23:53551328-53551328 - J33_T COSM3965371 c.9924G>A p.E3308E Substitution - coding silent 23:53548055-53548055 - S00539 COSM5658972 c.444C>A p.I148I Substitution - coding silent 23:53645371-53645371 - TCGA-G4-6302-01 COSM3694650 c.4726A>G p.K1576E Substitution - Missense 23:53584210-53584210 - TCGA-AN-A0AK-01 COSM3845072 c.88A>G p.N30D Substitution - Missense 23:53648268-53648268 - TCGA-HJ-7597-01 COSM4110139 c.12230G>A p.R4077H Substitution - Missense 23:53535473-53535473 - TCGA-A8-A09M-01 COSM3845035 c.11940G>T p.G3980G Substitution - coding silent 23:53538393-53538393 - TCGA-B5-A0JY-01 COSM1123202 c.5125G>T p.E1709* Substitution - Nonsense 23:53584222-53584222 - TCGA-BP-4774-01 COSM2968567 c.3249G>T p.R1083S Substitution - Missense 23:53595318-53595318 - YUGEMA COSM5412852 c.8040C>T p.F2680F Substitution - coding silent 23:53558775-53558775 - 8051974 COSM3390713 c.9412C>T p.R3138C Substitution - Missense 23:53550742-53550742 - TCGA-A2-A3XY-01 COSM3845032 c.12341C>T p.A4114V Substitution - Missense 23:53534676-53534676 - LOXIMVI COSM1682634 c.10506C>G p.D3502E Substitution - Missense 23:53546515-53546515 - SNU-175 COSM2968350 c.9891C>T p.S3297S Substitution - coding silent 23:53548088-53548088 - LUAD-B02077 COSM356285 c.1078C>G p.P360A Substitution - Missense 23:53628788-53628788 - YUPROST COSM1715007 c.759G>C p.K253N Substitution - Missense 23:53631417-53631417 - Pat_32_B COSM5878056 c.6906_6908delGGA p.E2303delE Deletion - In frame 23:53562130-53562132 - TCGA-BS-A0UF-01 COSM1123067 c.12588C>A p.I4196I Substitution - coding silent 23:53535445-53535445 - TCGA-AP-A0LM-01 COSM1123126 c.9304C>A p.L3102I Substitution - Missense 23:53549360-53549360 - TCGA-AP-A056-01 COSM1123146 c.7561C>T p.L2521F Substitution - Missense 23:53559004-53559004 - TCGA-AN-A046-01 COSM3845029 c.13101C>T p.C4367C Substitution - coding silent 23:53533333-53533333 - TCGA-BS-A0UF-01 COSM1123139 c.8513G>A p.R2838K Substitution - Missense 23:53552875-53552875 - CHC1061T COSM250784 c.7866C>G p.Y2622* Substitution - Nonsense 23:53554895-53554895 - PD3890a COSM219182 c.4910C>T p.T1637I Substitution - Missense 23:53583757-53583757 - TCGA-CD-8535-01 COSM4110181 c.5044C>T p.L1682L Substitution - coding silent 23:53583623-53583623 - TCGA-GF-A3OT-06 COSM3562348 c.12207C>T p.I4069I Substitution - coding silent 23:53536598-53536598 - TCGA-AP-A056-01 COSM1123172 c.6623G>A p.G2208D Substitution - Missense 23:53568776-53568776 - TCGA-IR-A3LK-01 COSM4817900 c.995C>G p.T332R Substitution - Missense 23:53628871-53628871 - I2L-P19Tb-Tumor-Biopsy COSM5367075 c.12006C>T p.R4002R Substitution - coding silent 23:53537687-53537687 - T3049 COSM3390714 c.9082C>T p.R3028C Substitution - Missense 23:53550742-53550742 - PAPLDL COSM5004428 c.3833G>A p.C1278Y Substitution - Missense 23:53592537-53592537 - D01 COSM5543928 c.3227G>A p.G1076E Substitution - Missense 23:53595340-53595340 - 215 COSM4424615 c.818G>A p.R273Q Substitution - Missense 23:53630979-53630979 - TCGA-BS-A0UF-01 COSM1123187 c.5299G>T p.G1767* Substitution - Nonsense 23:53580837-53580837 - TCGA-B5-A11E-01 COSM1123104 c.10867C>A p.L3623I Substitution - Missense 23:53544614-53544614 - PD5008a COSM3719490 c.11405A>G p.K3802R Substitution - Missense 23:53538978-53538978 - 5_FL COSM4171956 c.4188A>T p.L1396F Substitution - Missense 23:53588397-53588397 - SNUH_G76_S1 COSM4419894 c.2109A>G p.S703S Substitution - coding silent 23:53614686-53614686 - T1154 COSM4691576 c.8543T>C p.V2848A Substitution - Missense 23:53552845-53552845 - ESCC-D7 COSM5046453 c.94G>A p.E32K Substitution - Missense 23:53648262-53648262 - PD8984a COSM5769413 c.10553G>A p.R3518H Substitution - Missense 23:53546468-53546468 - TCGA-B0-5712-01 COSM1497255 c.11814A>G p.I3938M Substitution - Missense 23:53536661-53536661 - YUOTHO COSM5412849 c.9417G>A p.E3139E Substitution - coding silent 23:53549247-53549247 - T2940 COSM4691581 c.7261G>T p.G2421C Substitution - Missense 23:53560252-53560252 - CHC1556T COSM4787714 c.10797T>A p.S3599S Substitution - coding silent 23:53544684-53544684 - TARGET-30-PARHUX COSM1285456 c.8530G>T p.A2844S Substitution - Missense 23:53552858-53552858 - TCGA-A8-A09A-01 COSM457756 c.1805G>C p.G602A Substitution - Missense 23:53617122-53617122 - LUAD-E01014 COSM403502 c.717C>T p.I239I Substitution - coding silent 23:53631459-53631459 - 587220 COSM1210157 c.148G>A p.E50K Substitution - Missense 23:53647571-53647571 - TCGA-61-1900-01 COSM1331790 c.391G>T p.V131L Substitution - Missense 23:53645424-53645424 - TCGA-EI-6882-01 COSM3424859 c.7294C>T p.R2432C Substitution - Missense 23:53560219-53560219 - TCGA-66-2759-01 COSM756888 c.2177C>G p.S726C Substitution - Missense 23:53614618-53614618 - TCGA-60-2710-01 COSM756926 c.10715T>A p.V3572E Substitution - Missense 23:53546747-53546747 - HCC2998 COSM1682625 c.11356C>T p.R3786W Substitution - Missense 23:53543864-53543864 - TCGA-FU-A3TX-01 COSM4849372 c.11707C>T p.R3903W Substitution - Missense 23:53537656-53537656 - 61 COSM5742292 c.12577G>T p.G4193W Substitution - Missense 23:53535456-53535456 - S00837 COSM5701642 c.9778_9779GG>CT p.G3260L Substitution - Missense 23:53549215-53549216 - TCGA-D3-A2J8-06 COSM3562416 c.344C>T p.S115F Substitution - Missense 23:53647375-53647375 - HCC2998 COSM1682630 c.10850T>G p.L3617R Substitution - Missense 23:53544631-53544631 - TCGA-D3-A3C7-06 COSM3562366 c.10040T>A p.F3347Y Substitution - Missense 23:53548269-53548269 - CHC892T COSM4796435 c.6525G>A p.R2175R Substitution - coding silent 23:53568874-53568874 - ATL032 COSM5711709 c.10012C>G p.L3338V Substitution - Missense 23:53547967-53547967 - TCGA-EE-A2MR-06 COSM3562400 c.2763C>T p.S921S Substitution - coding silent 23:53603481-53603481 - TCGA-CG-4449-01 COSM4110143 c.12134G>A p.R4045Q Substitution - Missense 23:53537559-53537559 - TCGA-CG-4449-01 COSM4110144 c.11804G>A p.R3935Q Substitution - Missense 23:53537559-53537559 - TCGA-25-1630-01 COSM77874 c.1141C>A p.Q381K Substitution - Missense 23:53628594-53628594 - Gp2D COSM2968565 c.3294G>A p.A1098A Substitution - coding silent 23:53595273-53595273 - TCGA-BR-4292-01 COSM4110167 c.7572C>T p.D2524D Substitution - coding silent 23:53560352-53560352 - CSCC-49-T COSM3562378 c.8082G>A p.R2694R Substitution - coding silent 23:53558733-53558733 - NCI-H23 COSM1196502 c.10621A>T p.T3541S Substitution - Missense 23:53547688-53547688 - OSCC-GB_00920111 COSM4881791 c.11912G>T p.R3971L Substitution - Missense 23:53538421-53538421 - 587344 COSM1210162 c.11024C>T p.A3675V Substitution - Missense 23:53543866-53543866 - TCGA-G2-A3VY-01 COSM3800671 c.10136C>T p.S3379F Substitution - Missense 23:53548173-53548173 - YUPAER COSM5412855 c.6100G>A p.E2034K Substitution - Missense 23:53569629-53569629 - TCGA-AP-A051-01 COSM1123059 c.12908C>T p.T4303I Substitution - Missense 23:53534121-53534121 - Gp2D COSM2968549 c.3697T>A p.F1233I Substitution - Missense 23:53593408-53593408 - TCGA-BR-6452-01 COSM4110178 c.5603A>G p.N1868S Substitution - Missense 23:53580944-53580944 - T407 COSM4691587 c.6781G>A p.A2261T Substitution - Missense 23:53562843-53562843 - TCGA-29-1777-01 COSM1331796 c.9691C>A p.Q3231K Substitution - Missense 23:53549303-53549303 - TCGA-D1-A103-01 COSM1123132 c.9200G>A p.G3067E Substitution - Missense 23:53549464-53549464 - TCGA-B5-A11E-01 COSM1123074 c.11897C>A p.P3966H Substitution - Missense 23:53536578-53536578 - 188 COSM1741676 c.5725A>G p.K1909E Substitution - Missense 23:53573926-53573926 - TCGA-B7-5816-01 COSM4110190 c.2517A>C p.K839N Substitution - Missense 23:53604814-53604814 - T3104 COSM4691563 c.11976C>T p.L3992L Substitution - coding silent 23:53538357-53538357 - 526T COSM4383219 c.10798A>G p.M3600V Substitution - Missense 23:53544683-53544683 - TARGET-30-PAPLSD COSM1285455 c.5728G>A p.E1910K Substitution - Missense 23:53573923-53573923 - SJTALL005 COSM305980 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - TCGA-B7-5816-01 COSM2968412 c.7630G>A p.G2544R Substitution - Missense 23:53560294-53560294 - 201 COSM3722120 c.4944C>T p.L1648L Substitution - coding silent 23:53583723-53583723 - TCGA-RP-A695-06 COSM4896892 c.4594A>G p.N1532D Substitution - Missense 23:53584342-53584342 - S0045 COSM5885059 c.883G>T p.E295* Substitution - Nonsense 23:53629596-53629596 - CHEWS002 COSM4589483 c.9756G>A p.E3252E Substitution - coding silent 23:53548223-53548223 - RK076_C01 COSM2968568 c.3180C>T p.G1060G Substitution - coding silent 23:53595387-53595387 - TCGA-ER-A19S-06 COSM3562378 c.8082G>A p.R2694R Substitution - coding silent 23:53558733-53558733 - TCGA-BP-4991-01 COSM488478 c.4457G>T p.R1486L Substitution - Missense 23:53585145-53585145 - TCGA-BR-4361-01 COSM4110186 c.2791C>T p.L931L Substitution - coding silent 23:53603453-53603453 - CSCC-56-T COSM4472036 c.1756C>A p.L586M Substitution - Missense 23:53617363-53617363 - RK130_C01 COSM1636576 c.1527A>G p.K509K Substitution - coding silent 23:53625221-53625221 - CHC1556T COSM4787713 c.11127T>A p.S3709S Substitution - coding silent 23:53544684-53544684 - DLBCL-PatientD COSM220316 c.10562G>A p.G3521D Substitution - Missense 23:53546459-53546459 - TCGA-16-1045-01 COSM3406483 c.4552C>T p.R1518* Substitution - Nonsense 23:53585050-53585050 - TCGA-HM-A3JK-01 COSM4854893 c.4129A>G p.I1377V Substitution - Missense 23:53588456-53588456 - SWE-8 COSM1178735 c.2688C>T p.L896L Substitution - coding silent 23:53604643-53604643 - BD114T COSM5504775 c.585A>G p.A195A Substitution - coding silent 23:53632547-53632547 - 585267 COSM325519 c.2758A>G p.I920V Substitution - Missense 23:53603486-53603486 - TCGA-29-1691-01 COSM1331793 c.2926T>C p.L976L Substitution - coding silent 23:53595230-53595230 - RK119_C01 COSM3766993 c.10913T>A p.I3638K Substitution - Missense 23:53546438-53546438 - TCGA-BR-8487-01 COSM4110162 c.8071A>C p.R2691R Substitution - coding silent 23:53554690-53554690 - Pat_08_B COSM5878055 c.7317_7319delGGA p.E2440delE Deletion - In frame 23:53562130-53562132 - 1N64-VS-1T64 COSM4978097 c.7008G>A p.V2336V Substitution - coding silent 23:53564595-53564595 - T207 COSM4691590 c.5641A>G p.N1881D Substitution - Missense 23:53580906-53580906 - TCGA-46-3769-01 COSM756881 c.516A>T p.G172G Substitution - coding silent 23:53634287-53634287 - CSCC-60-T COSM4522819 c.11482G>T p.E3828* Substitution - Nonsense 23:53538901-53538901 - TCGA-A3-3374-01 COSM1497257 c.12799A>T p.N4267Y Substitution - Missense 23:53533407-53533407 - ESCC-F51 COSM5047979 c.4066C>A p.P1356T Substitution - Missense 23:53591029-53591029 - AOCS-092-3-3 COSM4149126 c.1978G>A p.G660R Substitution - Missense 23:53615815-53615815 - BCM759T COSM5348804 c.1952_1953insATCC p.L652fs*15 Insertion - Frameshift 23:53616974-53616975 - TCGA-AP-A051-01 COSM1123083 c.11942C>A p.P3981H Substitution - Missense 23:53538391-53538391 - TCGA-BL-A3JM-01 COSM1315601 c.402C>T p.V134V Substitution - coding silent 23:53645413-53645413 - TCGA-BR-8078-01 COSM4110146 c.11339A>G p.H3780R Substitution - Missense 23:53539044-53539044 - TCGA-FW-A3R5-06 COSM3914075 c.4697C>T p.P1566L Substitution - Missense 23:53586827-53586827 - TCGA-CJ-4900-01 COSM1497251 c.6214A>G p.M2072V Substitution - Missense 23:53568774-53568774 - CMLPh-002 COSM1285459 c.9146G>C p.S3049T Substitution - Missense 23:53550678-53550678 - sysucc-783T COSM5485168 c.6065C>T p.A2022V Substitution - Missense 23:53569664-53569664 - S02384 COSM5698689 c.3775C>T p.R1259W Substitution - Missense 23:53592595-53592595 - TCGA-HE-7130-01 COSM3722114 c.2197G>A p.E733K Substitution - Missense 23:53614598-53614598 - TCGA-06-1804-01 COSM3406480 c.6210T>C p.T2070T Substitution - coding silent 23:53573852-53573852 - B59-Tumor COSM1757282 c.3538G>A p.V1180I Substitution - Missense 23:53592421-53592421 - CSCC-18-T COSM4572874 c.8916T>A p.F2972L Substitution - Missense 23:53551446-53551446 - DF01 COSM5759345 c.612A>C p.A204A Substitution - coding silent 23:53632520-53632520 - TCGA-14-1823-01 COSM220519 c.6670G>A p.G2224R Substitution - Missense 23:53563770-53563770 - TCGA-CF-A27C-01 COSM1315598 c.2709C>G p.I903M Substitution - Missense 23:53604622-53604622 - TCGA-D8-A27F-01 COSM1491089 c.7976G>A p.G2659E Substitution - Missense 23:53554785-53554785 - SNU-175 COSM2968522 c.4627C>T p.L1543L Substitution - coding silent 23:53584309-53584309 - AOCS-164-1-7 COSM4422234 c.6516T>A p.T2172T Substitution - coding silent 23:53564676-53564676 - BD124T COSM5494284 c.694-8delT p.? Unknown 23:53631490-53631490 - MedB-1 COSM5621019 c.10243G>A p.A3415T Substitution - Missense 23:53548066-53548066 - HT115 COSM1123065 c.12777C>T p.I4259I Substitution - coding silent 23:53534570-53534570 - TCGA-B5-A0JY-01 COSM1123086 c.11539C>T p.R3847C Substitution - Missense 23:53538844-53538844 - TCGA-A7-A26F-01 COSM3845066 c.3818C>A p.A1273D Substitution - Missense 23:53589779-53589779 - H23 COSM1196502 c.10621A>T p.T3541S Substitution - Missense 23:53547688-53547688 - TCGA-EE-A3JI-06 COSM3562360 c.10900C>T p.L3634F Substitution - Missense 23:53546451-53546451 - B104-0 COSM1757275 c.9860C>T p.S3287L Substitution - Missense 23:53549134-53549134 - Gp5D COSM2968617 c.1259G>A p.G420D Substitution - Missense 23:53627863-53627863 - T2944 COSM4691562 c.12004C>T p.R4002C Substitution - Missense 23:53536471-53536471 - PM-2 COSM5619728 c.4205G>A p.R1402Q Substitution - Missense 23:53589803-53589803 - 2011-2373:2012-1301-T COSM4604254 c.12868G>C p.E4290Q Substitution - Missense 23:53533338-53533338 - TCGA-EK-A3GJ-01 COSM4852570 c.6841G>T p.E2281* Substitution - Nonsense 23:53562197-53562197 - HCC033T COSM5817921 c.11918C>T p.S3973F Substitution - Missense 23:53538415-53538415 - TCGA-AA-3713-01 COSM1468586 c.9997A>G p.I3333V Substitution - Missense 23:53547982-53547982 - TCGA-AP-A059-01 COSM1123228 c.2797G>A p.V933I Substitution - Missense 23:53603447-53603447 - TCGA-AC-A5XS-01 COSM261351 c.12650G>A p.R4217Q Substitution - Missense 23:53534049-53534049 - 1517_PT COSM5757551 c.9424T>C p.Y3142H Substitution - Missense 23:53550730-53550730 - TCGA-16-1045-01 COSM3406482 c.4963C>T p.R1655* Substitution - Nonsense 23:53585050-53585050 - TCGA-AP-A0LM-01 COSM1123128 c.9219C>T p.H3073H Substitution - coding silent 23:53549445-53549445 - TCGA-12-0616 COSM2153569 c.9281G>A p.R3094H Substitution - Missense 23:53549383-53549383 - TCGA-EI-6882-01 COSM3424858 c.7705C>T p.R2569C Substitution - Missense 23:53560219-53560219 - CHC1745T COSM4805848 c.10702G>T p.G3568C Substitution - Missense 23:53545045-53545045 - TCGA-D1-A103-01 COSM1123167 c.6225C>A p.I2075I Substitution - coding silent 23:53568763-53568763 - 2492723 COSM5723309 c.8477C>T p.S2826F Substitution - Missense 23:53554650-53554650 - CSCC-27-T COSM4506399 c.7198C>T p.R2400* Substitution - Nonsense 23:53562837-53562837 - TCGA-B5-A0JY-01 COSM1123207 c.4199T>G p.F1400C Substitution - Missense 23:53588386-53588386 - ME009T COSM224122 c.5792C>T p.T1931I Substitution - Missense 23:53573859-53573859 - TCGA-A8-A09I-01 COSM457741 c.12832G>C p.E4278Q Substitution - Missense 23:53533374-53533374 - TCGA-D3-A2JO-06 COSM3562383 c.6230G>A p.R2077Q Substitution - Missense 23:53568758-53568758 - 2012-1349:2012-1312-T COSM4604541 c.1792C>A p.R598S Substitution - Missense 23:53617135-53617135 - PT38 COSM3562390 c.4429C>T p.R1477C Substitution - Missense 23:53589579-53589579 - TCGA-BI-A0VR-01 COSM462204 c.12942C>T p.L4314L Substitution - coding silent 23:53534087-53534087 - CLL135 COSM1293033 c.3329A>C p.K1110T Substitution - Missense 23:53593365-53593365 - CLN4 COSM5024736 c.2825G>T p.C942F Substitution - Missense 23:53600125-53600125 - TCGA-B5-A11E-01 COSM1123103 c.11197C>A p.L3733I Substitution - Missense 23:53544614-53544614 - 2492729 COSM5726788 c.326C>T p.S109F Substitution - Missense 23:53647393-53647393 - TCGA-AX-A0J1-01 COSM1123135 c.8840C>T p.P2947L Substitution - Missense 23:53552352-53552352 - TCGA-B6-A0I6-01 COSM457745 c.11910G>C p.L3970F Substitution - Missense 23:53536565-53536565 - LS180 COSM2968546 c.3455A>G p.E1152G Substitution - Missense 23:53592504-53592504 - TCGA-BS-A0UV-01 COSM1123199 c.4846G>T p.D1616Y Substitution - Missense 23:53583821-53583821 - TCGA-EW-A1PC-01 COSM3845033 c.12472G>A p.V4158I Substitution - Missense 23:53536206-53536206 - TCGA-BR-4184-01 COSM4110191 c.2210C>T p.A737V Substitution - Missense 23:53614585-53614585 - TCGA-D3-A2JC-06 COSM3562381 c.6319A>G p.N2107D Substitution - Missense 23:53565217-53565217 - PD9567a COSM5801343 c.1460_1462delAAG p.E487delE Deletion - In frame 23:53627437-53627439 - Gp2D COSM2968371 c.9511A>G p.T3171A Substitution - Missense 23:53549483-53549483 - CSCC-31-T COSM4492199 c.3934C>T p.R1312C Substitution - Missense 23:53592436-53592436 - TCGA-AP-A056-01 COSM1123082 c.11663G>A p.R3888H Substitution - Missense 23:53538340-53538340 - Pat_55_A COSM5878057 c.5172_5173GG>AA p.A1725T Substitution - Missense 23:53583905-53583906 - 3N63-VS-3T63 COSM4984617 c.1033A>G p.S345G Substitution - Missense 23:53628833-53628833 - TCGA-D8-A1JA-01 COSM3845045 c.10130C>G p.S3377* Substitution - Nonsense 23:53548179-53548179 - TCGA-BS-A0UV-01 COSM1123071 c.12250T>C p.S4084P Substitution - Missense 23:53536555-53536555 - TCGA-AX-A0J0-01 COSM1123077 c.12118G>T p.E4040* Substitution - Nonsense 23:53537575-53537575 - TCGA-BR-4292-01 COSM4110168 c.7161C>T p.D2387D Substitution - coding silent 23:53560352-53560352 - TCGA-BS-A0UF-01 COSM1123158 c.6569C>A p.S2190* Substitution - Nonsense 23:53564623-53564623 - TCGA-BR-6452-01 COSM4110179 c.5192A>G p.N1731S Substitution - Missense 23:53580944-53580944 - TCGA-A2-A3XT-01 COSM3845047 c.9964G>A p.V3322I Substitution - Missense 23:53549030-53549030 - TCGA-12-0616-01 COSM2153569 c.9281G>A p.R3094H Substitution - Missense 23:53549383-53549383 - TCGA-BR-8487-01 COSM4110169 c.7373A>G p.D2458G Substitution - Missense 23:53561890-53561890 - XHDG39 COSM4770035 c.7634G>A p.R2545H Substitution - Missense 23:53560290-53560290 - TCGA-AP-A0LM-01 COSM1123229 c.2359G>T p.D787Y Substitution - Missense 23:53607660-53607660 - HT-29 COSM1682632 c.10565A>C p.Y3522S Substitution - Missense 23:53546456-53546456 - TCGA-G4-6302-01 COSM3694647 c.7320A>G p.E2440E Substitution - coding silent 23:53562129-53562129 - CHC892T COSM4796435 c.6525G>A p.R2175R Substitution - coding silent 23:53568874-53568874 - I2L-P10-Tumor-Organoid COSM5366793 c.10742T>C p.V3581A Substitution - Missense 23:53544739-53544739 - CSCC-60-T COSM4522818 c.11812G>T p.E3938* Substitution - Nonsense 23:53538901-53538901 - PT33 COSM5910015 c.10721C>T p.S3574F Substitution - Missense 23:53546741-53546741 - sysucc-627T COSM5468123 c.10334G>A p.R3445Q Substitution - Missense 23:53547975-53547975 - ATL027 COSM5711707 c.11737C>T p.R3913C Substitution - Missense 23:53537626-53537626 - LUAD-NYU739 COSM376327 c.6458T>A p.V2153E Substitution - Missense 23:53569682-53569682 - TCGA-EE-A2GO-06 COSM3562411 c.1414C>T p.P472S Substitution - Missense 23:53627485-53627485 - SJLGG037_D COSM1716225 c.7035G>A p.E2345E Substitution - coding silent 23:53563816-53563816 - 18472 COSM5616342 c.5972A>G p.Y1991C Substitution - Missense 23:53575701-53575701 - TCGA-BR-A4QL-01 COSM4110202 c.794A>G p.H265R Substitution - Missense 23:53631003-53631003 - TCGA-B5-A11E-01 COSM1123250 c.391G>A p.V131M Substitution - Missense 23:53645424-53645424 - 116 COSM4169977 c.6694+2T>C p.? Unknown 23:53563744-53563744 - TCGA-A8-A0A6-01 COSM3845058 c.6038T>G p.V2013G Substitution - Missense 23:53569691-53569691 - LS180 COSM2968508 c.5030A>G p.N1677S Substitution - Missense 23:53583637-53583637 - COLO205 COSM612992 c.2034G>T p.T678T Substitution - coding silent 23:53615759-53615759 - Gp5D COSM2968372 c.9181A>G p.T3061A Substitution - Missense 23:53549483-53549483 - Gp2D COSM2968372 c.9181A>G p.T3061A Substitution - Missense 23:53549483-53549483 - TCGA-28-5218-01 COSM3406476 c.11410C>T p.R3804W Substitution - Missense 23:53542509-53542509 - TCGA-BR-8680-01 COSM4110152 c.10250T>C p.V3417A Substitution - Missense 23:53547729-53547729 - TCGA-IR-A3LI-01 COSM4846211 c.8617G>A p.D2873N Substitution - Missense 23:53552771-53552771 - AB COSM5414947 c.9765G>T p.R3255R Substitution - coding silent 23:53548214-53548214 - CCK81 COSM2968618 c.1125G>T p.M375I Substitution - Missense 23:53628610-53628610 - TCGA-FW-A3R5-06 COSM3914078 c.3688C>T p.L1230F Substitution - Missense 23:53590496-53590496 - CSCC-27-T COSM4506400 c.6787C>T p.R2263* Substitution - Nonsense 23:53562837-53562837 - OSCC-GB_01380111 COSM5953762 c.3700G>A p.E1234K Substitution - Missense 23:53590484-53590484 - D1 COSM5007716 c.1958G>A p.G653E Substitution - Missense 23:53615835-53615835 - TCGA-BT-A0YX-01 COSM422537 c.7659G>A p.L2553L Substitution - coding silent 23:53560265-53560265 - 06-15922 COSM220519 c.6670G>A p.G2224R Substitution - Missense 23:53563770-53563770 - sysucc-863T COSM2153569 c.9281G>A p.R3094H Substitution - Missense 23:53549383-53549383 - TCGA-EE-A29L-06 COSM3562399 c.2960C>T p.P987L Substitution - Missense 23:53595196-53595196 - CSCC-20-T COSM4448737 c.11831_11833delAAG p.E3944delE Deletion - In frame 23:53536642-53536644 - BRC11 COSM5028930 c.5333G>A p.R1778K Substitution - Missense 23:53577040-53577040 - BD171T COSM5494821 c.10981G>A p.E3661K Substitution - Missense 23:53543909-53543909 - 35M COSM5581338 c.4425C>T p.S1475S Substitution - coding silent 23:53585177-53585177 - BD241T COSM5497439 c.1834T>C p.C612R Substitution - Missense 23:53617093-53617093 - TCGA-EJ-5508-01 COSM3783611 c.824A>G p.Q275R Substitution - Missense 23:53630973-53630973 - TCGA-IR-A3LK-01 COSM4816595 c.13069C>T p.R4357C Substitution - Missense 23:53533365-53533365 - TCGA-EB-A42Y-01 COSM3562364 c.10418A>G p.Q3473R Substitution - Missense 23:53547891-53547891 - TCGA-21-1070-01 COSM756922 c.10582G>T p.V3528L Substitution - Missense 23:53547727-53547727 - SJOS004_D COSM5023549 c.3040C>G p.H1014D Substitution - Missense 23:53594551-53594551 - TCGA-BP-4774-01 COSM23130 c.2838G>T p.R946S Substitution - Missense 23:53595318-53595318 - TCGA-61-1900-01 COSM1331795 c.8790G>T p.E2930D Substitution - Missense 23:53551166-53551166 - HCT-116 COSM1682639 c.6484C>T p.R2162W Substitution - Missense 23:53569656-53569656 - 2011-2366:2012-1295-T COSM4605449 c.4704C>G p.L1568L Substitution - coding silent 23:53586820-53586820 - TCGA-13-0885-01 COSM81284 c.9006G>C p.L3002L Substitution - coding silent 23:53550950-53550950 - PD3890a COSM219182 c.4910C>T p.T1637I Substitution - Missense 23:53583757-53583757 - TCGA-IR-A3LK-01 COSM4817525 c.7306G>A p.E2436K Substitution - Missense 23:53562143-53562143 - T3021 COSM50797 c.9470G>A p.R3157H Substitution - Missense 23:53549194-53549194 - TCGA-AX-A2H5-01 COSM1123143 c.8116G>A p.D2706N Substitution - Missense 23:53558699-53558699 - TCGA-ER-A19F-06 COSM3562404 c.1961A>C p.D654A Substitution - Missense 23:53615832-53615832 - ESCC_4 COSM5623035 c.12852A>G p.L4284L Substitution - coding silent 23:53533354-53533354 - VLTS-5 COSM5702734 c.153A>T p.L51F Substitution - Missense 23:53647566-53647566 - TCGA-46-3769-01 COSM756878 c.515G>T p.G172V Substitution - Missense 23:53634288-53634288 - sysucc-1030T COSM5452361 c.10505A>G p.D3502G Substitution - Missense 23:53546516-53546516 - LC_S18 COSM1190562 c.5599A>G p.I1867V Substitution - Missense 23:53580948-53580948 - TCGA-EB-A431-01 COSM3562363 c.10245C>T p.T3415T Substitution - coding silent 23:53547734-53547734 - TCGA-A3-3316-01 COSM1497252 c.7441C>T p.R2481* Substitution - Nonsense 23:53561822-53561822 - B96 COSM1757279 c.8131G>A p.D2711N Substitution - Missense 23:53558684-53558684 - HCC96T COSM3708671 c.11956G>C p.V3986L Substitution - Missense 23:53538377-53538377 - TCGA-EE-A182-06 COSM3562352 c.12100C>T p.L4034L Substitution - coding silent 23:53537593-53537593 - LS411 COSM2968636 c.692A>G p.K231R Substitution - Missense 23:53631568-53631568 - LUAD-GU4I3 COSM367850 c.8882G>A p.R2961H Substitution - Missense 23:53551074-53551074 - TCGA-EE-A3AE-06 COSM3914079 c.3907G>A p.D1303N Substitution - Missense 23:53592463-53592463 - CHC429T COSM5349423 c.1813C>G p.P605A Substitution - Missense 23:53617114-53617114 - 2492703 COSM5715750 c.8820C>T p.S2940S Substitution - coding silent 23:53552372-53552372 - TCGA-CM-6674-01 COSM1468596 c.7300C>T p.P2434S Substitution - Missense 23:53560213-53560213 - pfg103T COSM4755430 c.6131A>G p.K2044R Substitution - Missense 23:53573931-53573931 - B96-Tumor COSM1757280 c.7720G>A p.D2574N Substitution - Missense 23:53558684-53558684 - TCGA-BR-A4PD-01 COSM4110184 c.3235G>T p.V1079F Substitution - Missense 23:53595332-53595332 - EWS502 COSM4589486 c.3495T>C p.A1165A Substitution - coding silent 23:53594507-53594507 - 041T COSM1729601 c.9811A>T p.S3271C Substitution - Missense 23:53548168-53548168 - CCK81 COSM2968249 c.12445A>G p.I4149V Substitution - Missense 23:53534572-53534572 - TCGA-LL-A5YN-01 COSM4391464 c.2740C>G p.Q914E Substitution - Missense 23:53604591-53604591 - pfg151T COSM4755420 c.12038G>A p.R4013Q Substitution - Missense 23:53537655-53537655 - App2312 COSM4169092 c.8762A>G p.E2921G Substitution - Missense 23:53551270-53551270 - KYSE-180 COSM756912 c.9169G>T p.D3057Y Substitution - Missense 23:53551117-53551117 - TCGA-G2-A3VY-01 COSM3800672 c.9806C>T p.S3269F Substitution - Missense 23:53548173-53548173 - PAPNNX COSM2968491 c.5975G>A p.R1992Q Substitution - Missense 23:53575698-53575698 - TCGA-B0-5712-01 COSM1497254 c.12144A>G p.I4048M Substitution - Missense 23:53536661-53536661 - TCGA-BH-A18G-01 COSM3845063 c.4285G>A p.D1429N Substitution - Missense 23:53589723-53589723 - sysucc-311T COSM5467901 c.5716+9C>T p.? Unknown 23:53580822-53580822 - CCK81 COSM2968625 c.780_781delCA p.I261fs*8 Deletion - Frameshift 23:53631016-53631017 - TCGA-BR-7707-01 COSM4110165 c.7814G>A p.R2605H Substitution - Missense 23:53559455-53559455 - RK130_C01 COSM1636575 c.1527A>G p.K509K Substitution - coding silent 23:53625221-53625221 - SW403 COSM4655473 c.8217C>T p.S2739S Substitution - coding silent 23:53552841-53552841 - TCGA-ER-A19M-06 COSM3562370 c.9684C>T p.S3228S Substitution - coding silent 23:53549310-53549310 - ESCC_4 COSM5623034 c.13080A>G p.L4360L Substitution - coding silent 23:53533354-53533354 - TCGA-AP-A051-01 COSM1123196 c.5317G>T p.D1773Y Substitution - Missense 23:53583761-53583761 - PT34 COSM5911131 c.12259G>A p.D4087N Substitution - Missense 23:53536546-53536546 - TCGA-33-4532-01 COSM756917 c.10117A>G p.T3373A Substitution - Missense 23:53547862-53547862 - PD22357a COSM5784092 c.8666C>A p.T2889N Substitution - Missense 23:53552722-53552722 - Mx43 COSM50187 c.12280_12282delAAG p.K4094del Deletion - In frame 23:53535421-53535423 - TCGA-BQ-5875-01 COSM3992538 c.12005G>A p.R4002H Substitution - Missense 23:53537688-53537688 - TCGA-BS-A0UF-01 COSM1123193 c.5056C>T p.L1686F Substitution - Missense 23:53583611-53583611 - CHC1211T COSM4955001 c.9326G>T p.R3109L Substitution - Missense 23:53549338-53549338 - TCGA-13-0887-01 COSM4946832 c.9097-1G>T p.? Unknown 23:53551190-53551190 - TCGA-AP-A0LM-01 COSM1123142 c.7911G>T p.K2637N Substitution - Missense 23:53554850-53554850 - pfg005T COSM4755426 c.7050C>A p.D2350E Substitution - Missense 23:53563801-53563801 - 585272 COSM325521 c.12188G>A p.R4063Q Substitution - Missense 23:53536617-53536617 - sysucc-1510T COSM5764101 c.10631G>A p.R3544Q Substitution - Missense 23:53545116-53545116 - LUAD-S01409 COSM388237 c.9772G>T p.G3258C Substitution - Missense 23:53548207-53548207 - TCGA-D1-A17Q-01 COSM1123251 c.349G>T p.E117* Substitution - Nonsense 23:53647370-53647370 - Gp2D COSM2968616 c.1259G>A p.G420D Substitution - Missense 23:53627863-53627863 - NPC42F COSM4997148 c.5834A>G p.Y1945C Substitution - Missense 23:53573817-53573817 - TCGA-ED-A459-01 COSM4935658 c.386A>T p.Q129L Substitution - Missense 23:53645429-53645429 - 392 COSM3722114 c.2197G>A p.E733K Substitution - Missense 23:53614598-53614598 - TCGA-BP-4352-01 COSM3364166 c.7957G>A p.E2653K Substitution - Missense 23:53559019-53559019 - 2011-2373:2012-1301-T COSM457741 c.12832G>C p.E4278Q Substitution - Missense 23:53533374-53533374 - OSCC-GB_01240111 COSM5954143 c.12412G>A p.E4138K Substitution - Missense 23:53534605-53534605 - C709 COSM4444199 c.6920A>G p.D2307G Substitution - Missense 23:53564683-53564683 - TCGA-C5-A1MK-01 COSM4826821 c.8492G>A p.R2831Q Substitution - Missense 23:53552370-53552370 - 90879 COSM329406 c.6349T>C p.S2117P Substitution - Missense 23:53565187-53565187 - ESO-640 COSM1254539 c.1018A>G p.T340A Substitution - Missense 23:53628848-53628848 - 2492712 COSM5718834 c.2833-7C>T p.? Unknown 23:53595330-53595330 - TCGA-A8-A06Z-01 COSM3845042 c.10521C>T p.D3507D Substitution - coding silent 23:53546500-53546500 - TCGA-DK-A1A6-01 COSM1315590 c.9144G>A p.Q3048Q Substitution - coding silent 23:53551142-53551142 - CSCC-41-T COSM4509333 c.8041C>T p.L2681L Substitution - coding silent 23:53558774-53558774 - OSCC-GB_00530111 COSM4883294 c.2500C>A p.L834M Substitution - Missense 23:53604831-53604831 - TCGA-GV-A3JX-01 COSM1315594 c.4130G>C p.R1377T Substitution - Missense 23:53590465-53590465 - OSCC-GB_00670111 COSM4883908 c.1489+1G>T p.? Unknown 23:53627409-53627409 - TCGA-46-6025-01 COSM756912 c.9169G>T p.D3057Y Substitution - Missense 23:53551117-53551117 - 53M COSM5594698 c.1005C>T p.V335V Substitution - coding silent 23:53628861-53628861 - TCGA-DM-A1DA-01 COSM3694644 c.12064C>T p.R4022C Substitution - Missense 23:53537629-53537629 - 2492720 COSM5723310 c.8111C>T p.S2704F Substitution - Missense 23:53554650-53554650 - ESCC-038T COSM3940042 c.10871T>C p.L3624P Substitution - Missense 23:53546480-53546480 - RK183_C01 COSM3766999 c.4771G>T p.D1591Y Substitution - Missense 23:53586543-53586543 - TCGA-DM-A1DA-01 COSM191505 c.11734C>T p.R3912C Substitution - Missense 23:53537629-53537629 - SJACT005_D COSM4968004 c.6826G>C p.E2276Q Substitution - Missense 23:53562212-53562212 - TCGA-43-6770-01 COSM756902 c.6777G>C p.Q2259H Substitution - Missense 23:53565170-53565170 - TCGA-BS-A0UV-01 COSM1123092 c.11181G>T p.K3727N Substitution - Missense 23:53539778-53539778 - TCGA-AP-A0LM-01 COSM1123113 c.10538C>T p.S3513F Substitution - Missense 23:53547771-53547771 - I2L-P5-Tumor-Organoid COSM5367339 c.5987G>A p.R1996H Substitution - Missense 23:53575686-53575686 - YUJUBE COSM5412846 c.10571C>T p.S3524F Substitution - Missense 23:53547738-53547738 - MSK-PCa1_organoid COSM5423580 c.961_962insA p.M321fs*4 Insertion - Frameshift 23:53629517-53629518 - TCGA-EE-A2GM-06 COSM3562396 c.3474C>T p.L1158L Substitution - coding silent 23:53594528-53594528 - T155 COSM1176457 c.7808G>A p.R2603Q Substitution - Missense 23:53559461-53559461 - TCGA-EE-A29D-06 COSM3562377 c.7964C>T p.P2655L Substitution - Missense 23:53554797-53554797 - TCGA-B5-A0JY-01 COSM1123111 c.10614G>A p.T3538T Substitution - coding silent 23:53547695-53547695 - TCGA-61-1900-01 COSM1331794 c.9120G>T p.E3040D Substitution - Missense 23:53551166-53551166 - TCGA-CG-5720-01 COSM4110140 c.12448G>C p.D4150H Substitution - Missense 23:53536230-53536230 - BN24 COSM1625987 c.2283T>C p.R761R Substitution - coding silent 23:53608888-53608888 - TARGET-30-PAPLSD COSM1285454 c.6139G>A p.E2047K Substitution - Missense 23:53573923-53573923 - HCC2218 COSM23130 c.2838G>T p.R946S Substitution - Missense 23:53595318-53595318 - ATL032 COSM5711708 c.10342C>G p.L3448V Substitution - Missense 23:53547967-53547967 - TCGA-B5-A0JY-01 COSM1123148 c.7561C>A p.L2521I Substitution - Missense 23:53559004-53559004 - TCGA-AP-A059-01 COSM1123133 c.9332G>A p.R3111H Substitution - Missense 23:53550954-53550954 - TCGA-EE-A2GM-06 COSM3562384 c.6101C>T p.S2034L Substitution - Missense 23:53573961-53573961 - HN_62861 COSM123680 c.12035G>A p.R4012H Substitution - Missense 23:53536440-53536440 - TCGA-BR-8680-01 COSM4110183 c.4375A>G p.T1459A Substitution - Missense 23:53586528-53586528 - cSCCP4 COSM139242 c.11764C>T p.R3922C Substitution - Missense 23:53537599-53537599 - TCGA-66-2773-01 COSM756890 c.2332G>A p.E778K Substitution - Missense 23:53607687-53607687 - E20 COSM1666208 c.5971A>C p.T1991P Substitution - Missense 23:53569758-53569758 - 2492701 COSM5715751 c.8490C>T p.S2830S Substitution - coding silent 23:53552372-53552372 - CLL119 COSM1293030 c.6775C>T p.Q2259* Substitution - Nonsense 23:53565172-53565172 - TCGA-DK-A1A6-01 COSM1315592 c.9111G>C p.Q3037H Substitution - Missense 23:53551175-53551175 - TCGA-D1-A16X-01 COSM1123237 c.1801C>A p.L601I Substitution - Missense 23:53617126-53617126 - sysucc-1163T COSM2968523 c.5027G>A p.R1676H Substitution - Missense 23:53584320-53584320 - TCGA-ER-A19S-06 COSM3562379 c.7671G>A p.R2557R Substitution - coding silent 23:53558733-53558733 - T256 COSM4691568 c.9504G>A p.K3168K Substitution - coding silent 23:53549160-53549160 - B104-0-Tumor COSM1757276 c.9530C>T p.S3177L Substitution - Missense 23:53549134-53549134 - TCGA-EE-A2GO-06 COSM3562359 c.11152G>T p.D3718Y Substitution - Missense 23:53539807-53539807 - TCGA-AP-A051-01 COSM1123174 c.6520G>A p.A2174T Substitution - Missense 23:53569620-53569620 - TCGA-AP-A0LG-01 COSM1123188 c.5669A>G p.N1890S Substitution - Missense 23:53580878-53580878 - RK180_C02 COSM1636569 c.10211G>C p.G3404A Substitution - Missense 23:53548098-53548098 - TCGA-C5-A7CL-01 COSM4837835 c.1931G>A p.R644Q Substitution - Missense 23:53616996-53616996 - S01023 COSM5666903 c.11953C>A p.L3985M Substitution - Missense 23:53538380-53538380 - 61 COSM5742295 c.11702G>A p.G3901E Substitution - Missense 23:53537661-53537661 - ICC009T COSM5823559 c.6612C>T p.T2204T Substitution - coding silent 23:53568787-53568787 - TCGA-D9-A6EA-06 COSM4398471 c.11896C>T p.P3966S Substitution - Missense 23:53536579-53536579 - TCGA-CG-5722-01 COSM4110200 c.1031G>T p.S344I Substitution - Missense 23:53628835-53628835 - TCGA-CJ-4897-01 COSM488483 c.84T>G p.V28V Substitution - coding silent 23:53648272-53648272 - BD171T COSM5494820 c.11311G>A p.E3771K Substitution - Missense 23:53543909-53543909 - PTC-28C COSM4156910 c.3934C>G p.R1312G Substitution - Missense 23:53592436-53592436 - CSCC-49-T COSM3562379 c.7671G>A p.R2557R Substitution - coding silent 23:53558733-53558733 - OSCC-GB_01360111 COSM5955646 c.12433G>A p.D4145N Substitution - Missense 23:53536245-53536245 - CSCC-18-T COSM4513699 c.9480C>T p.S3160S Substitution - coding silent 23:53550674-53550674 - VLTS-5 COSM5702735 c.153A>T p.L51F Substitution - Missense 23:53647566-53647566 - TCGA-CG-5720-01 COSM4110141 c.12118G>C p.D4040H Substitution - Missense 23:53536230-53536230 - 2293776 COSM4608091 c.4311G>T p.Q1437H Substitution - Missense 23:53586802-53586802 - TCGA-A6-5665-01 COSM1468583 c.10815A>G p.L3605L Substitution - coding silent 23:53546536-53546536 - TCGA-AP-A0LM-01 COSM1123114 c.10208C>T p.S3403F Substitution - Missense 23:53547771-53547771 - TTC466 COSM4589485 c.8285G>T p.G2762V Substitution - Missense 23:53552773-53552773 - TCGA-B5-A11N-01 COSM1123231 c.2354C>T p.T785I Substitution - Missense 23:53607665-53607665 - I2L-P10-Tumor-Organoid COSM5366792 c.11072T>C p.V3691A Substitution - Missense 23:53544739-53544739 - TCGA-AP-A051-01 COSM1123197 c.4906G>T p.D1636Y Substitution - Missense 23:53583761-53583761 - TCGA-G9-7510-01 COSM1472219 c.4006A>G p.M1336V Substitution - Missense 23:53591089-53591089 - SA235 COSM212783 c.12289G>A p.V4097I Substitution - Missense 23:53535414-53535414 - HCC96 COSM3708671 c.11956G>C p.V3986L Substitution - Missense 23:53538377-53538377 - TCGA-BR-A4CS-01 COSM4110174 c.7033G>A p.E2345K Substitution - Missense 23:53563818-53563818 - 2011-2289:2012-1332-T COSM4604425 c.1591+1G>T p.? Unknown 23:53625156-53625156 - TCGA-66-2734-01 COSM756899 c.4836C>A p.G1612G Substitution - coding silent 23:53583831-53583831 - SNUH_G26_S1 COSM4002321 c.9360A>G p.A3120A Substitution - coding silent 23:53550926-53550926 - LUAD_E00522 COSM388778 c.5929G>A p.G1977S Substitution - Missense 23:53575744-53575744 - 587284 COSM1210169 c.1240A>G p.K414E Substitution - Missense 23:53628495-53628495 - T3038 COSM4691583 c.6969C>T p.D2323D Substitution - coding silent 23:53561883-53561883 - PD8637a COSM3720358 c.7073T>C p.F2358S Substitution - Missense 23:53561779-53561779 - PD8637a COSM3720357 c.7484T>C p.F2495S Substitution - Missense 23:53561779-53561779 - TCGA-CD-8535-01 COSM4110180 c.5455C>T p.L1819L Substitution - coding silent 23:53583623-53583623 - TCGA-D3-A1QB-06 COSM3562393 c.3751C>T p.P1251S Substitution - Missense 23:53590433-53590433 - PT34 COSM5911133 c.1783C>T p.P595S Substitution - Missense 23:53617144-53617144 - T3724 COSM4691595 c.2673T>G p.P891P Substitution - coding silent 23:53604658-53604658 - TCGA-B5-A11E-01 COSM1123180 c.6129G>T p.K2043N Substitution - Missense 23:53573933-53573933 - BD114T COSM5504776 c.585A>G p.A195A Substitution - coding silent 23:53632547-53632547 - TCGA-66-2734-01 COSM756898 c.5247C>A p.G1749G Substitution - coding silent 23:53583831-53583831 - SJLGG037_D COSM1716226 c.6624G>A p.E2208E Substitution - coding silent 23:53563816-53563816 - TCGA-EZ-7264-01 COSM3973736 c.3973C>G p.L1325V Substitution - Missense 23:53591122-53591122 - TCGA-D1-A17Q-01 COSM1123252 c.349G>T p.E117* Substitution - Nonsense 23:53647370-53647370 - TCGA-AD-6964-01 COSM1468601 c.4790C>T p.A1597V Substitution - Missense 23:53586524-53586524 - TCGA-D1-A17A-01 COSM1123168 c.6635T>G p.I2212S Substitution - Missense 23:53568764-53568764 - YUAKER COSM1715004 c.3404C>T p.S1135L Substitution - Missense 23:53592555-53592555 - LUAD-S01346 COSM404348 c.12526C>T p.R4176C Substitution - Missense 23:53534173-53534173 - RK197_C01 COSM3766995 c.10462T>A p.S3488T Substitution - Missense 23:53547847-53547847 - PTC-14C COSM4156907 c.6706G>T p.G2236* Substitution - Nonsense 23:53562918-53562918 - LUAD-B00416 COSM355518 c.861A>G p.L287L Substitution - coding silent 23:53630936-53630936 - TCGA-HJ-7597-01 COSM4110138 c.12560G>A p.R4187H Substitution - Missense 23:53535473-53535473 - TCGA-B5-A0JY-01 COSM1123217 c.3568G>T p.D1190Y Substitution - Missense 23:53591116-53591116 - 2293776 COSM4608090 c.4722G>T p.Q1574H Substitution - Missense 23:53586802-53586802 - TCGA-AP-A0LM-01 COSM1123125 c.9634C>A p.L3212I Substitution - Missense 23:53549360-53549360 - TCGA-ES-A2HS-01 COSM4910589 c.8507C>A p.P2836Q Substitution - Missense 23:53552881-53552881 - 1N58-VS-1T58 COSM4977520 c.12896A>G p.*4299* Substitution - coding silent 23:53533310-53533310 - CHC1745T COSM4805847 c.11032G>T p.G3678C Substitution - Missense 23:53545045-53545045 - TCGA-AN-A046-01 COSM3845030 c.12873C>T p.C4291C Substitution - coding silent 23:53533333-53533333 - TCGA-FW-A3R5-06 COSM3914076 c.4286C>T p.P1429L Substitution - Missense 23:53586827-53586827 - COLO201 COSM612992 c.2034G>T p.T678T Substitution - coding silent 23:53615759-53615759 - HX32T COSM3708673 c.3816G>T p.S1272S Substitution - coding silent 23:53592554-53592554 - TCGA-AP-A056-01 COSM1123066 c.12447C>T p.I4149I Substitution - coding silent 23:53534570-53534570 - sysucc-783T COSM5485169 c.3291C>T p.A1097A Substitution - coding silent 23:53595276-53595276 - TCGA-B3-8121-01 COSM3992542 c.7236G>A p.E2412E Substitution - coding silent 23:53562213-53562213 - sysucc-1512T COSM5450821 c.1071A>G p.G357G Substitution - coding silent 23:53628795-53628795 - TCGA-43-5668-01 COSM756876 c.145T>C p.C49R Substitution - Missense 23:53647574-53647574 - sysucc-1163T COSM5459517 c.9422A>C p.Q3141P Substitution - Missense 23:53550732-53550732 - TCGA-AP-A051-01 COSM1123060 c.12578C>T p.T4193I Substitution - Missense 23:53534121-53534121 - TCGA-B5-A11E-01 COSM1123061 c.12860C>A p.S4287Y Substitution - Missense 23:53534169-53534169 - BN24 COSM1625988 c.2283T>C p.R761R Substitution - coding silent 23:53608888-53608888 - TCGA-EE-A2GJ-06 COSM3562391 c.4018C>T p.R1340C Substitution - Missense 23:53589579-53589579 - CSCC-41-T COSM4555323 c.6502G>A p.E2168K Substitution - Missense 23:53569638-53569638 - YUJUBE COSM5412847 c.10241C>T p.S3414F Substitution - Missense 23:53547738-53547738 - 577-01-4TD COSM5418130 c.1297G>A p.V433I Substitution - Missense 23:53627825-53627825 - DF01 COSM5759346 c.612A>C p.A204A Substitution - coding silent 23:53632520-53632520 - LUAD-B00416 COSM355520 c.216G>A p.V72V Substitution - coding silent 23:53647503-53647503 - TCGA-HE-7130-01 COSM3722113 c.2197G>A p.E733K Substitution - Missense 23:53614598-53614598 - TCGA-24-1614-01 COSM77873 c.5665T>C p.S1889P Substitution - Missense 23:53575176-53575176 - 61 COSM5742297 c.10993A>G p.I3665V Substitution - Missense 23:53543897-53543897 - D1 COSM5007715 c.1958G>A p.G653E Substitution - Missense 23:53615835-53615835 - OSCC-GB_00540111 COSM4889547 c.11554C>G p.H3852D Substitution - Missense 23:53538449-53538449 - TCGA-BR-8487-01 COSM4110154 c.10172C>T p.T3391M Substitution - Missense 23:53547807-53547807 - 201 COSM3722119 c.5355C>T p.L1785L Substitution - coding silent 23:53583723-53583723 - TCGA-AX-A0J0-01 COSM1123233 c.2348A>G p.N783S Substitution - Missense 23:53607671-53607671 - YUAKER COSM1714998 c.7135C>T p.H2379Y Substitution - Missense 23:53560378-53560378 - RKO COSM2968510 c.4980A>G p.E1660E Substitution - coding silent 23:53583687-53583687 - HCC19T COSM1625991 c.1310A>G p.D437G Substitution - Missense 23:53627812-53627812 - TCGA-BS-A0UJ-01 COSM1123107 c.10861A>G p.K3621E Substitution - Missense 23:53546490-53546490 - YUKAT COSM5412860 c.2146C>T p.P716S Substitution - Missense 23:53614649-53614649 - TCGA-06-0876 COSM2152061 c.10551C>T p.A3517A Substitution - coding silent 23:53546470-53546470 - TCGA-B0-5085-01 COSM488482 c.259G>C p.E87Q Substitution - Missense 23:53647460-53647460 - TCGA-AP-A051-01 COSM1123236 c.2084C>A p.P695H Substitution - Missense 23:53614711-53614711 - TCGA-BS-A0UV-01 COSM1123205 c.4223C>T p.A1408V Substitution - Missense 23:53586890-53586890 - TCGA-BS-A0UF-01 COSM1123157 c.6980C>A p.S2327* Substitution - Nonsense 23:53564623-53564623 - PA285 COSM1163763 c.7882_7883delTT p.F2628fs*2 Deletion - Frameshift 23:53559386-53559387 - OSCC-GB_00880111 COSM4888027 c.11212C>A p.R3738S Substitution - Missense 23:53544599-53544599 - CSCC-27-T COSM4564190 c.10217_10218CC>TT p.A3406V Substitution - Missense 23:53547761-53547762 - TCGA-BR-4292-01 COSM4110172 c.6897G>A p.E2299E Substitution - coding silent 23:53562141-53562141 - RK007_C01 COSM1636574 c.7548A>C p.E2516D Substitution - Missense 23:53559017-53559017 - TCGA-AP-A0LM-01 COSM1123141 c.8277G>T p.K2759N Substitution - Missense 23:53554850-53554850 - TCGA-AX-A0J0-01 COSM1123234 c.2348A>G p.N783S Substitution - Missense 23:53607671-53607671 - TCGA-AP-A051-01 COSM1123235 c.2084C>A p.P695H Substitution - Missense 23:53614711-53614711 - TCGA-F4-6459-01 COSM1468563 c.12309G>C p.M4103I Substitution - Missense 23:53535394-53535394 - YUAKER COSM1714997 c.7546C>T p.H2516Y Substitution - Missense 23:53560378-53560378 - TCGA-FS-A1YW-06 COSM3562394 c.3594C>T p.F1198F Substitution - coding silent 23:53593511-53593511 - SJACT005_D COSM4968003 c.7237G>C p.E2413Q Substitution - Missense 23:53562212-53562212 - CSCC-27-T COSM4494127 c.4275C>T p.F1425F Substitution - coding silent 23:53589733-53589733 - 2492714 COSM5718833 c.3237C>T p.V1079V Substitution - coding silent 23:53595330-53595330 - YUZINO COSM1715002 c.3658C>T p.P1220S Substitution - Missense 23:53591026-53591026 - 585272 COSM325520 c.11858G>A p.R3953Q Substitution - Missense 23:53536617-53536617 - CMLPh-002 COSM1285458 c.9476G>C p.S3159T Substitution - Missense 23:53550678-53550678 - MO_1316 COSM5549201 c.6581C>A p.A2194D Substitution - Missense 23:53564611-53564611 - TCGA-A2-A1FW-01 COSM1491097 c.1583T>C p.I528T Substitution - Missense 23:53625165-53625165 - TCGA-B5-A0JY-01 COSM1123211 c.4085C>A p.A1362D Substitution - Missense 23:53588500-53588500 - B104-0 COSM1757276 c.9530C>T p.S3177L Substitution - Missense 23:53549134-53549134 - TCGA-EZ-7264-01 COSM3973737 c.3562C>G p.L1188V Substitution - Missense 23:53591122-53591122 - LUAD-E01014 COSM403503 c.717C>T p.I239I Substitution - coding silent 23:53631459-53631459 - SJTALL005 COSM305980 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - 587284 COSM1210168 c.12374C>T p.P4125L Substitution - Missense 23:53534643-53534643 - TCGA-FS-A1YW-06 COSM3562395 c.3183C>T p.F1061F Substitution - coding silent 23:53593511-53593511 - TCGA-CG-5723-01 COSM4110164 c.7481A>G p.Q2494R Substitution - Missense 23:53559377-53559377 - CHC1211T COSM4955000 c.9656G>T p.R3219L Substitution - Missense 23:53549338-53549338 - TCGA-BR-8296-01 COSM2968366 c.9364C>T p.R3122C Substitution - Missense 23:53549300-53549300 - 61 COSM5742299 c.5737C>T p.R1913W Substitution - Missense 23:53573914-53573914 - TCGA-CZ-5985-01 COSM488479 c.4600A>T p.T1534S Substitution - Missense 23:53588396-53588396 - 2492711 COSM5718834 c.2833-7C>T p.? Unknown 23:53595330-53595330 - TCGA-21-1078-01 COSM756910 c.8485C>G p.P2829A Substitution - Missense 23:53554642-53554642 - T1154 COSM4691579 c.7902T>G p.S2634S Substitution - coding silent 23:53554859-53554859 - 587350 COSM1210165 c.7561C>T p.R2521C Substitution - Missense 23:53560363-53560363 - 3N38-VS-3T38 COSM4981449 c.9550G>A p.E3184K Substitution - Missense 23:53549444-53549444 - OSCC-GB_01060111 COSM4882830 c.7018C>A p.Q2340K Substitution - Missense 23:53564585-53564585 - PD3890a COSM219182 c.4910C>T p.T1637I Substitution - Missense 23:53583757-53583757 - HCC19T COSM1625990 c.1310A>G p.D437G Substitution - Missense 23:53627812-53627812 - TCGA-D3-A2JC-06 COSM3562380 c.6730A>G p.N2244D Substitution - Missense 23:53565217-53565217 - Mx34 COSM50795 c.11915G>A p.R3972H Substitution - Missense 23:53536560-53536560 - TCGA-BS-A0UJ-01 COSM1123219 c.3243T>C p.S1081S Substitution - coding silent 23:53593451-53593451 - TCGA-AA-3713-01 COSM1468585 c.10327A>G p.I3443V Substitution - Missense 23:53547982-53547982 - HCC2998 COSM1682630 c.10850T>G p.L3617R Substitution - Missense 23:53544631-53544631 - Gp2D COSM2968550 c.3286T>A p.F1096I Substitution - Missense 23:53593408-53593408 - TCGA-D1-A103-01 COSM1123201 c.4835G>T p.G1612V Substitution - Missense 23:53583832-53583832 - 587302 COSM1210155 c.12679T>G p.L4227V Substitution - Missense 23:53534668-53534668 - TCGA-BR-4362-01 COSM2968644 c.329G>A p.R110Q Substitution - Missense 23:53647390-53647390 - TCGA-FR-A3YO-06 COSM3562374 c.8469G>A p.M2823I Substitution - Missense 23:53554658-53554658 - OSCC-GB_00530111 COSM4883295 c.2500C>A p.L834M Substitution - Missense 23:53604831-53604831 - Patient_1 COSM5414245 c.11980C>T p.L3994F Substitution - Missense 23:53536495-53536495 - TCGA-CG-5721-01 COSM50795 c.11915G>A p.R3972H Substitution - Missense 23:53536560-53536560 - 2492712 COSM5718833 c.3237C>T p.V1079V Substitution - coding silent 23:53595330-53595330 - TCGA-EE-A2GM-06 COSM3562385 c.5690C>T p.S1897L Substitution - Missense 23:53573961-53573961 - TCGA-EE-A29M-06 COSM3562356 c.11522C>T p.P3841L Substitution - Missense 23:53539767-53539767 - TCGA-66-2759-01 COSM756887 c.2177C>G p.S726C Substitution - Missense 23:53614618-53614618 - TCGA-ER-A19S-06 COSM3562406 c.1960G>A p.D654N Substitution - Missense 23:53615833-53615833 - I2L-P20-Tumor-Biopsy COSM5367221 c.3374G>A p.R1125Q Substitution - Missense 23:53595193-53595193 - S02139 COSM5674739 c.6071G>T p.G2024V Substitution - Missense 23:53569658-53569658 - 40 COSM4169975 c.4641G>T p.R1547S Substitution - Missense 23:53584295-53584295 - TCGA-AX-A2H5-01 COSM1123144 c.7705G>A p.D2569N Substitution - Missense 23:53558699-53558699 - PD5008a COSM3719489 c.11735A>G p.K3912R Substitution - Missense 23:53538978-53538978 - T3262 COSM4691566 c.11294C>T p.A3765V Substitution - Missense 23:53539665-53539665 - 587234 COSM1210174 c.8684C>T p.A2895V Substitution - Missense 23:53551348-53551348 - TCGA-B8-4143-01 COSM488475 c.7845C>A p.I2615I Substitution - coding silent 23:53559424-53559424 - LIM1215 COSM4379675 c.2650A>G p.T884A Substitution - Missense 23:53604681-53604681 - 3N63-VS-3T63 COSM4984618 c.1033A>G p.S345G Substitution - Missense 23:53628833-53628833 - CCK81 COSM2968619 c.1125G>T p.M375I Substitution - Missense 23:53628610-53628610 - B104-0-Tumor COSM1757275 c.9860C>T p.S3287L Substitution - Missense 23:53549134-53549134 - HT29 COSM1682631 c.10895A>C p.Y3632S Substitution - Missense 23:53546456-53546456 - TCGA-L6-A4EP-01 COSM3372294 c.1403G>A p.R468Q Substitution - Missense 23:53627496-53627496 - BD241T COSM5497440 c.1834T>C p.C612R Substitution - Missense 23:53617093-53617093 - S01563 COSM5670134 c.6718G>A p.A2240T Substitution - Missense 23:53565229-53565229 - 29T COSM3713965 c.7205-1G>C p.? Unknown 23:53562245-53562245 - HCT15 COSM1682637 c.9646G>A p.A3216T Substitution - Missense 23:53549348-53549348 - TCGA-AA-3966-01 COSM272788 c.3812G>T p.R1271L Substitution - Missense 23:53589785-53589785 - TCGA-D1-A17Q-01 COSM1123070 c.12113G>T p.S4038I Substitution - Missense 23:53536235-53536235 - T155 COSM1176458 c.7397G>A p.R2466Q Substitution - Missense 23:53559461-53559461 - HCC2218 COSM23130 c.2838G>T p.R946S Substitution - Missense 23:53595318-53595318 - TCGA-BR-8368-01 COSM4110150 c.10498C>T p.R3500W Substitution - Missense 23:53546523-53546523 - TCGA-AA-A010-01 COSM281812 c.6229C>T p.R2077W Substitution - Missense 23:53568759-53568759 - AOCS-164-1-7 COSM4422233 c.6927T>A p.T2309T Substitution - coding silent 23:53564676-53564676 - HCC2998 COSM1682628 c.10966C>T p.R3656W Substitution - Missense 23:53543924-53543924 - pfg173T COSM4755429 c.6232C>A p.L2078I Substitution - Missense 23:53568756-53568756 - TCGA-AN-A0XW-01 COSM457758 c.529T>A p.F177I Substitution - Missense 23:53634274-53634274 - TCGA-A2-A0T5-01 COSM3845052 c.7207A>C p.T2403P Substitution - Missense 23:53560306-53560306 - QC2-32-T2 COSM4419894 c.2109A>G p.S703S Substitution - coding silent 23:53614686-53614686 - PDA_049 COSM5000639 c.8397G>T p.Q2799H Substitution - Missense 23:53554730-53554730 - YUPTER COSM5412858 c.3723C>T p.F1241F Substitution - coding silent 23:53593382-53593382 - 2492700 COSM5715751 c.8490C>T p.S2830S Substitution - coding silent 23:53552372-53552372 - H23 COSM1196503 c.10291A>T p.T3431S Substitution - Missense 23:53547688-53547688 - 07-058 COSM3736502 c.12491A>C p.N4164T Substitution - Missense 23:53534526-53534526 - 2492713 COSM5718834 c.2833-7C>T p.? Unknown 23:53595330-53595330 - TCGA-EE-A29L-06 COSM3562398 c.3371C>T p.P1124L Substitution - Missense 23:53595196-53595196 - 587302 COSM1210156 c.12349T>G p.L4117V Substitution - Missense 23:53534668-53534668 - 2492723 COSM5723310 c.8111C>T p.S2704F Substitution - Missense 23:53554650-53554650 - OSCC-GB_01240111 COSM5954142 c.12742G>A p.E4248K Substitution - Missense 23:53534605-53534605 - HCC058T COSM5805544 c.4689A>T p.L1563L Substitution - coding silent 23:53584247-53584247 - 1N58-VS-1T58 COSM4977519 c.13124A>G p.*4375* Substitution - coding silent 23:53533310-53533310 - TCGA-AP-A051-01 COSM1123119 c.10248C>T p.G3416G Substitution - coding silent 23:53548061-53548061 - DM851T COSM673989 c.8632C>A p.Q2878K Substitution - Missense 23:53551400-53551400 - ESCC-F87 COSM5048970 c.12321C>G p.F4107L Substitution - Missense 23:53536484-53536484 - SC_9037 COSM5558940 c.5892G>A p.L1964L Substitution - coding silent 23:53573759-53573759 - 2492701 COSM5715750 c.8820C>T p.S2940S Substitution - coding silent 23:53552372-53552372 - TCGA-BR-4368-01 COSM1176457 c.7808G>A p.R2603Q Substitution - Missense 23:53559461-53559461 - 1517_PT COSM5757552 c.9094T>C p.Y3032H Substitution - Missense 23:53550730-53550730 - HCC2998 COSM1682626 c.11026C>T p.R3676W Substitution - Missense 23:53543864-53543864 - TCGA-BR-4368-01 COSM1176458 c.7397G>A p.R2466Q Substitution - Missense 23:53559461-53559461 - 3N50-VS-3T50 COSM4983208 c.5620-1G>A p.? Unknown 23:53575222-53575222 - STC248 COSM5064762 c.4884G>A p.M1628I Substitution - Missense 23:53583783-53583783 - ESCC-D20 COSM5046020 c.8814G>T p.Q2938H Substitution - Missense 23:53551142-53551142 - TCGA-B5-A0JY-01 COSM1123203 c.4714G>T p.E1572* Substitution - Nonsense 23:53584222-53584222 - TCGA-D9-A6EA-06 COSM4398470 c.12226C>T p.P4076S Substitution - Missense 23:53536579-53536579 - 8665_CLM COSM5757554 c.4264A>G p.K1422E Substitution - Missense 23:53586849-53586849 - KYSE180 COSM756912 c.9169G>T p.D3057Y Substitution - Missense 23:53551117-53551117 - TCGA-BR-6452-01 COSM4110196 c.1308T>C p.V436V Substitution - coding silent 23:53627814-53627814 - TCGA-B5-A11E-01 COSM1123249 c.391G>A p.V131M Substitution - Missense 23:53645424-53645424 - TCGA-34-5232-01 COSM756896 c.5103G>T p.E1701D Substitution - Missense 23:53584244-53584244 - TCGA-BR-A4QL-01 COSM4110201 c.794A>G p.H265R Substitution - Missense 23:53631003-53631003 - PTC-28C COSM4156904 c.9762G>T p.K3254N Substitution - Missense 23:53549232-53549232 - TCGA-ED-A459-01 COSM4935657 c.386A>T p.Q129L Substitution - Missense 23:53645429-53645429 - 3N38-VS-3T38 COSM4981450 c.9220G>A p.E3074K Substitution - Missense 23:53549444-53549444 - 188 COSM1741675 c.6136A>G p.K2046E Substitution - Missense 23:53573926-53573926 - 8058339 COSM3390712 c.12309G>A p.M4103I Substitution - Missense 23:53535394-53535394 - 116 COSM4169976 c.7105+2T>C p.? Unknown 23:53563744-53563744 - ESCC-175T COSM3940044 c.10665T>G p.S3555S Substitution - coding silent 23:53546797-53546797 - HCC96 COSM3708672 c.11626G>C p.V3876L Substitution - Missense 23:53538377-53538377 - TCGA-D1-A17F-01 COSM1123118 c.10052C>T p.S3351L Substitution - Missense 23:53547927-53547927 - TCGA-BR-4368-01 COSM220519 c.6670G>A p.G2224R Substitution - Missense 23:53563770-53563770 - TCGA-AP-A059-01 COSM1123134 c.9002G>A p.R3001H Substitution - Missense 23:53550954-53550954 - ESO-114 COSM1254535 c.1824C>T p.F608F Substitution - coding silent 23:53617103-53617103 - TCGA-D1-A17Q-01 COSM1123069 c.12443G>T p.S4148I Substitution - Missense 23:53536235-53536235 - CSCC-20-T COSM4448736 c.12161_12163delAAG p.E4054delE Deletion - In frame 23:53536642-53536644 - 587388 COSM1210172 c.11962C>T p.H3988Y Substitution - Missense 23:53536513-53536513 - TCGA-BR-A4PD-01 COSM4110185 c.2833-9G>T p.? Unknown 23:53595332-53595332 - PT26 COSM5905338 c.11968C>T p.R3990C Substitution - Missense 23:53538365-53538365 - PD9567a COSM5801344 c.1460_1462delAAG p.E487delE Deletion - In frame 23:53627437-53627439 - HN_62921 COSM123681 c.11929G>A p.D3977N Substitution - Missense 23:53536546-53536546 - TCGA-D1-A16D-01 COSM1123220 c.3641C>T p.T1214M Substitution - Missense 23:53593464-53593464 - TCGA-AD-6964-01 COSM1468602 c.4379C>T p.A1460V Substitution - Missense 23:53586524-53586524 - T3104 COSM4691564 c.11646C>T p.L3882L Substitution - coding silent 23:53538357-53538357 - ESCC-038T COSM3940043 c.10541T>C p.L3514P Substitution - Missense 23:53546480-53546480 - LUAD_E00522 COSM388779 c.5518G>A p.G1840S Substitution - Missense 23:53575744-53575744 - TCGA-BS-A0UF-01 COSM1123186 c.5710G>T p.G1904* Substitution - Nonsense 23:53580837-53580837 - TCGA-AX-A05Z-01 COSM1123240 c.1777G>T p.D593Y Substitution - Missense 23:53617342-53617342 - TCGA-FW-A3R5-06 COSM3914073 c.5168C>T p.P1723L Substitution - Missense 23:53583910-53583910 - sysucc-783T COSM5485167 c.6476C>T p.A2159V Substitution - Missense 23:53569664-53569664 - TCGA-EE-A3JB-06 COSM4898778 c.1425C>T p.I475I Substitution - coding silent 23:53627474-53627474 - BK0020 COSM4186261 c.10148C>A p.T3383N Substitution - Missense 23:53547831-53547831 - LC_C21 COSM1190560 c.10876G>A p.G3626R Substitution - Missense 23:53546475-53546475 - PT34 COSM123681 c.11929G>A p.D3977N Substitution - Missense 23:53536546-53536546 - BD114T COSM5504773 c.11394G>A p.Q3798Q Substitution - coding silent 23:53542525-53542525 - TCGA-33-4532-01 COSM756916 c.10447A>G p.T3483A Substitution - Missense 23:53547862-53547862 - TCGA-CM-6162-01 COSM1468604 c.4003A>G p.N1335D Substitution - Missense 23:53589594-53589594 - TCGA-AP-A056-01 COSM1123243 c.1557C>T p.I519I Substitution - coding silent 23:53625191-53625191 - 2011-2322:2012-352-T COSM4606111 c.8781G>T p.Q2927H Substitution - Missense 23:53551175-53551175 - PD24307a COSM5774406 c.3968G>A p.R1323H Substitution - Missense 23:53589629-53589629 - TCGA-AX-A060-01 COSM367850 c.8882G>A p.R2961H Substitution - Missense 23:53551074-53551074 - TCGA-AA-3663-01 COSM1468605 c.3646C>A p.L1216I Substitution - Missense 23:53593459-53593459 - TCGA-G4-6302-01 COSM3694645 c.10100G>T p.R3367M Substitution - Missense 23:53548209-53548209 - RK095_C01 COSM3701870 c.12481T>C p.Y4161H Substitution - Missense 23:53534536-53534536 - C709 COSM4444200 c.6509A>G p.D2170G Substitution - Missense 23:53564683-53564683 - TCGA-LL-A5YP-01 COSM4391491 c.5295G>T p.M1765I Substitution - Missense 23:53583783-53583783 - T3064 COSM4691573 c.9140delG p.G3047fs*13 Deletion - Frameshift 23:53550684-53550684 - 3N24-VS-3T24 COSM4979871 c.6014C>G p.S2005* Substitution - Nonsense 23:53575659-53575659 - EGC8 COSM5064760 c.12405G>A p.Q4135Q Substitution - coding silent 23:53534612-53534612 - KPOPBR-13-T COSM5963521 c.11224A>T p.S3742C Substitution - Missense 23:53539735-53539735 - DN1401D COSM5961308 c.11588G>T p.C3863F Substitution - Missense 23:53539701-53539701 - SJDOSTEOS006 COSM5759918 c.5151C>G p.T1717T Substitution - coding silent 23:53580985-53580985 - TCGA-HU-8602-01 COSM1123121 c.10093C>T p.R3365W Substitution - Missense 23:53548216-53548216 - LUAD-B02077 COSM356286 c.1078C>G p.P360A Substitution - Missense 23:53628788-53628788 - TCGA-C5-A7CL-01 COSM4837834 c.1931G>A p.R644Q Substitution - Missense 23:53616996-53616996 - Gp5D COSM2968550 c.3286T>A p.F1096I Substitution - Missense 23:53593408-53593408 - TCGA-D1-A103-01 COSM1123257 c.117G>A p.Q39Q Substitution - coding silent 23:53648239-53648239 - TCGA-BR-8368-01 COSM4110149 c.10828C>T p.R3610W Substitution - Missense 23:53546523-53546523 - 61 COSM5742294 c.12032G>A p.G4011E Substitution - Missense 23:53537661-53537661 - I2L-P20-Tumor-Biopsy COSM5367222 c.2963G>A p.R988Q Substitution - Missense 23:53595193-53595193 - RK229_C01 COSM4780361 c.6629A>G p.N2210S Substitution - Missense 23:53568770-53568770 - TCGA-B5-A0JY-01 COSM1123256 c.255A>C p.E85D Substitution - Missense 23:53647464-53647464 - TCGA-IR-A3LK-01 COSM4817526 c.6895G>A p.E2299K Substitution - Missense 23:53562143-53562143 - I2L-P19Tb-Tumor-Organoid COSM5367076 c.11676C>T p.R3892R Substitution - coding silent 23:53537687-53537687 - TCGA-BS-A0UV-01 COSM1123072 c.11920T>C p.S3974P Substitution - Missense 23:53536555-53536555 - TCGA-D3-A2JO-06 COSM3562382 c.6641G>A p.R2214Q Substitution - Missense 23:53568758-53568758 - TCGA-D1-A16X-01 COSM1123238 c.1801C>A p.L601I Substitution - Missense 23:53617126-53617126 - TCGA-B8-4143-01 COSM488476 c.7434C>A p.I2478I Substitution - coding silent 23:53559424-53559424 - TCGA-GF-A3OT-06 COSM3562349 c.11877C>T p.I3959I Substitution - coding silent 23:53536598-53536598 - OSCC-GB_00290111 COSM3713966 c.6794-1G>C p.? Unknown 23:53562245-53562245 - TCGA-FR-A3YO-06 COSM3562375 c.8103G>A p.M2701I Substitution - Missense 23:53554658-53554658 - TCGA-EE-A29C-06 COSM3562402 c.2593C>T p.P865S Substitution - Missense 23:53604738-53604738 - ESCC-F120 COSM5047134 c.8105_8106delCA p.T2702fs*4 Deletion - Frameshift 23:53558709-53558710 - BD124T COSM5494283 c.694-8delT p.? Unknown 23:53631490-53631490 - BD114T COSM5504774 c.11064G>A p.Q3688Q Substitution - coding silent 23:53542525-53542525 - 61 COSM5742296 c.11323A>G p.I3775V Substitution - Missense 23:53543897-53543897 - T3064 COSM4691572 c.9470delG p.G3157fs*13 Deletion - Frameshift 23:53550684-53550684 - TCGA-B0-5085-01 COSM488481 c.259G>C p.E87Q Substitution - Missense 23:53647460-53647460 - HCC1187 COSM23117 c.1442G>A p.R481K Substitution - Missense 23:53627457-53627457 - AOCS-092-3-3 COSM4149127 c.1978G>A p.G660R Substitution - Missense 23:53615815-53615815 - CHEWS002 COSM4589482 c.10086G>A p.E3362E Substitution - coding silent 23:53548223-53548223 - PD4952a COSM5787959 c.12012G>A p.E4004E Substitution - coding silent 23:53537681-53537681 - 587256 COSM1123097 c.11338C>T p.R3780C Substitution - Missense 23:53543882-53543882 - LS180 COSM2968507 c.5441A>G p.N1814S Substitution - Missense 23:53583637-53583637 - TCGA-BR-4363-01 COSM4110176 c.6187A>G p.K2063E Substitution - Missense 23:53573875-53573875 - TCGA-D8-A1XQ-01 COSM3845056 c.6761G>C p.S2254T Substitution - Missense 23:53562863-53562863 - S01023 COSM5666905 c.927G>A p.L309L Substitution - coding silent 23:53629552-53629552 - TCGA-D1-A101-01 COSM1123191 c.5093G>A p.R1698H Substitution - Missense 23:53583574-53583574 - TCGA-A8-A09M-01 COSM3845036 c.11610G>T p.G3870G Substitution - coding silent 23:53538393-53538393 - CHC1715T COSM4789410 c.2881G>T p.A961S Substitution - Missense 23:53595275-53595275 - PT34 COSM5911132 c.1783C>T p.P595S Substitution - Missense 23:53617144-53617144 - PD22360a COSM5796061 c.11383G>C p.E3795Q Substitution - Missense 23:53542536-53542536 - RK180_C02 COSM1636570 c.9881G>C p.G3294A Substitution - Missense 23:53548098-53548098 - RK183_C01 COSM3767000 c.4360G>T p.D1454Y Substitution - Missense 23:53586543-53586543 - YUGEMA COSM5412853 c.7629C>T p.F2543F Substitution - coding silent 23:53558775-53558775 - AA COSM5414948 c.1728C>A p.L576L Substitution - coding silent 23:53617391-53617391 - 587338 COSM1210163 c.12709C>T p.R4237C Substitution - Missense 23:53534638-53534638 - PCSI_0066_Pa_X COSM3379653 c.4782A>G p.E1594E Substitution - coding silent 23:53586532-53586532 - CSCC-38-T COSM4446201 c.1672+3_1672+4AA>GG p.? Unknown 23:53624591-53624592 - TCGA-BS-A0UV-01 COSM1123198 c.5257G>T p.D1753Y Substitution - Missense 23:53583821-53583821 - S00934 COSM5663010 c.11516C>T p.P3839L Substitution - Missense 23:53538867-53538867 - TCGA-BR-6852-01 COSM4110156 c.9944G>A p.S3315N Substitution - Missense 23:53548035-53548035 - HCT-15 COSM1682638 c.9316G>A p.A3106T Substitution - Missense 23:53549348-53549348 - ESCC-184T COSM3940041 c.12115G>A p.E4039K Substitution - Missense 23:53536233-53536233 - 1N64-VS-1T64 COSM4978098 c.6597G>A p.V2199V Substitution - coding silent 23:53564595-53564595 - TCGA-36-1577-01 COSM116655 c.8996A>G p.H2999R Substitution - Missense 23:53550960-53550960 - TCGA-AP-A0LM-01 COSM1123161 c.6883G>A p.E2295K Substitution - Missense 23:53564720-53564720 - TCGA-A6-5665-01 COSM1123214 c.4290G>A p.P1430P Substitution - coding silent 23:53589718-53589718 - SNU-175 COSM2968521 c.5038C>T p.L1680L Substitution - coding silent 23:53584309-53584309 - TCGA-ER-A19F-06 COSM3562403 c.1961A>C p.D654A Substitution - Missense 23:53615832-53615832 - S01522 COSM4386979 c.1934G>A p.R645K Substitution - Missense 23:53616993-53616993 - TCGA-BR-4357-01 COSM4110197 c.1042G>A p.D348N Substitution - Missense 23:53628824-53628824 - TCGA-HU-A4GU-01 COSM2968348 c.9912C>T p.S3304S Substitution - coding silent 23:53548067-53548067 - Pat_27_B COSM5878055 c.7317_7319delGGA p.E2440delE Deletion - In frame 23:53562130-53562132 - HCC107T COSM1625985 c.7460G>T p.R2487L Substitution - Missense 23:53561803-53561803 - T3049 COSM3390713 c.9412C>T p.R3138C Substitution - Missense 23:53550742-53550742 - SJLGG037 COSM1716225 c.7035G>A p.E2345E Substitution - coding silent 23:53563816-53563816 - TCGA-A8-A06X-01 COSM457749 c.10426G>C p.E3476Q Substitution - Missense 23:53546706-53546706 - TCGA-A6-6141-01 COSM1468621 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - Pat_54_A COSM3562372 c.9482A>G p.H3161R Substitution - Missense 23:53550672-53550672 - TCGA-BS-A0UJ-01 COSM1123218 c.3654T>C p.S1218S Substitution - coding silent 23:53593451-53593451 - CHC892T COSM4959885 c.12645C>T p.I4215I Substitution - coding silent 23:53534054-53534054 - 273T COSM1727384 c.6469G>A p.G2157S Substitution - Missense 23:53565067-53565067 - sysucc-863T COSM2153568 c.9611G>A p.R3204H Substitution - Missense 23:53549383-53549383 - TCGA-G4-6302-01 COSM3694648 c.6909A>G p.E2303E Substitution - coding silent 23:53562129-53562129 - TCGA-ES-A2HS-01 COSM4910590 c.8177C>A p.P2726Q Substitution - Missense 23:53552881-53552881 - Pat_24_B COSM5878053 c.7616T>A p.L2539H Substitution - Missense 23:53560308-53560308 - LUAD-B00416 COSM355517 c.9063C>T p.T3021T Substitution - coding silent 23:53550761-53550761 - PDA_049 COSM5000640 c.8031G>T p.Q2677H Substitution - Missense 23:53554730-53554730 - TCGA-FP-8631-01 COSM4110160 c.8250C>T p.S2750S Substitution - coding silent 23:53552808-53552808 - TCGA-AX-A0J0-01 COSM1123078 c.11788G>T p.E3930* Substitution - Nonsense 23:53537575-53537575 - SWE-54A COSM1178529 c.850A>G p.I284V Substitution - Missense 23:53630947-53630947 - TCGA-AX-A0J1-01 COSM1123136 c.8510C>T p.P2837L Substitution - Missense 23:53552352-53552352 - Pat_02_B COSM5878051 c.11216G>A p.R3739Q Substitution - Missense 23:53544595-53544595 - TCGA-B8-4621-01 COSM488474 c.8371C>A p.Q2791K Substitution - Missense 23:53552687-53552687 - 587344 COSM1210161 c.11354C>T p.A3785V Substitution - Missense 23:53543866-53543866 - LS174T COSM2968545 c.3866A>G p.E1289G Substitution - Missense 23:53592504-53592504 - TCGA-C5-A1MH-01 COSM4821042 c.7153G>A p.E2385K Substitution - Missense 23:53562882-53562882 - TCGA-AP-A056-01 COSM1123105 c.11095C>T p.P3699S Substitution - Missense 23:53544716-53544716 - GCT42 COSM1123161 c.6883G>A p.E2295K Substitution - Missense 23:53564720-53564720 - TCGA-AP-A0LM-01 COSM1123162 c.6472G>A p.E2158K Substitution - Missense 23:53564720-53564720 - LOXIMVI COSM1682633 c.10836C>G p.D3612E Substitution - Missense 23:53546515-53546515 - PD8984a COSM5769412 c.10883G>A p.R3628H Substitution - Missense 23:53546468-53546468 - TCGA-06-0876-01 COSM2152060 c.10881C>T p.A3627A Substitution - coding silent 23:53546470-53546470 - SJDOSTEOS006 COSM5759917 c.5562C>G p.T1854T Substitution - coding silent 23:53580985-53580985 - TCGA-D1-A103-01 COSM1123131 c.9530G>A p.G3177E Substitution - Missense 23:53549464-53549464 - HCC2218 COSM23130 c.2838G>T p.R946S Substitution - Missense 23:53595318-53595318 - TCGA-EJ-5508-01 COSM3783612 c.824A>G p.Q275R Substitution - Missense 23:53630973-53630973 - PD9585a COSM5779520 c.2957G>C p.G986A Substitution - Missense 23:53602578-53602578 - TCGA-CG-5722-01 COSM4110199 c.1031G>T p.S344I Substitution - Missense 23:53628835-53628835 - T3038 COSM4691582 c.7380C>T p.D2460D Substitution - coding silent 23:53561883-53561883 - 587306 COSM1210160 c.2738G>T p.G913V Substitution - Missense 23:53604593-53604593 - CLL119 COSM1293031 c.6364C>T p.Q2122* Substitution - Nonsense 23:53565172-53565172 - U2940 COSM5621017 c.11699T>C p.V3900A Substitution - Missense 23:53539014-53539014 - TCGA-BR-4184-01 COSM4110192 c.2210C>T p.A737V Substitution - Missense 23:53614585-53614585 - S01023 COSM5666904 c.11623C>A p.L3875M Substitution - Missense 23:53538380-53538380 - B96 COSM1757280 c.7720G>A p.D2574N Substitution - Missense 23:53558684-53558684 - 2492713 COSM5718833 c.3237C>T p.V1079V Substitution - coding silent 23:53595330-53595330 - TCGA-AU-6004-01 COSM1468607 c.3293C>T p.A1098V Substitution - Missense 23:53595274-53595274 - NYU939 COSM1210165 c.7561C>T p.R2521C Substitution - Missense 23:53560363-53560363 - TCGA-CM-6162-01 COSM1468603 c.4414A>G p.N1472D Substitution - Missense 23:53589594-53589594 - U2940 COSM5621018 c.11369T>C p.V3790A Substitution - Missense 23:53539014-53539014 - TCGA-D1-A17F-01 COSM1123117 c.10382C>T p.S3461L Substitution - Missense 23:53547927-53547927 - PT33 COSM5910016 c.10391C>T p.S3464F Substitution - Missense 23:53546741-53546741 - QC2-22-T2 COSM5653121 c.11606A>G p.D3869G Substitution - Missense 23:53538397-53538397 - TCGA-EK-A3GJ-01 COSM4852569 c.7252G>T p.E2418* Substitution - Nonsense 23:53562197-53562197 - CSCC-27-T COSM4490935 c.3304C>T p.L1102L Substitution - coding silent 23:53593390-53593390 - TCGA-AA-A02F-01 COSM287451 c.10842G>C p.L3614F Substitution - Missense 23:53544639-53544639 - 577-01-4TD COSM5418129 c.1297G>A p.V433I Substitution - Missense 23:53627825-53627825 - 2012-1348:2012-1317-T COSM4604179 c.12216G>C p.E4072D Substitution - Missense 23:53536589-53536589 - TCGA-BR-4184-01 COSM4110148 c.11072C>T p.A3691V Substitution - Missense 23:53542517-53542517 - HCT-116 COSM1682640 c.6073C>T p.R2025W Substitution - Missense 23:53569656-53569656 - TCGA-AP-A051-01 COSM1123254 c.277C>T p.L93F Substitution - Missense 23:53647442-53647442 - TCGA-DC-5869-01 COSM1570126 c.4948C>T p.R1650W Substitution - Missense 23:53583719-53583719 - TCGA-EW-A1IZ-01 COSM1491092 c.7317G>A p.E2439E Substitution - coding silent 23:53562132-53562132 - HT29 COSM1682632 c.10565A>C p.Y3522S Substitution - Missense 23:53546456-53546456 - PD3890a COSM4809958 c.5321C>T p.T1774I Substitution - Missense 23:53583757-53583757 - 587284 COSM1210170 c.1240A>G p.K414E Substitution - Missense 23:53628495-53628495 - HCC1187 COSM23117 c.1442G>A p.R481K Substitution - Missense 23:53627457-53627457 - HCT8 COSM4635814 c.8261C>T p.A2754V Substitution - Missense 23:53554866-53554866 - TCGA-B5-A0JY-01 COSM1123112 c.10284G>A p.T3428T Substitution - coding silent 23:53547695-53547695 - 2492729 COSM5726789 c.326C>T p.S109F Substitution - Missense 23:53647393-53647393 - CSCC-31-T COSM4508348 c.7309C>T p.P2437S Substitution - Missense 23:53560204-53560204 - T407 COSM4691598 c.273G>A p.M91I Substitution - Missense 23:53647446-53647446 - pfg144T COSM4755419 c.12315G>C p.M4105I Substitution - Missense 23:53535388-53535388 - TCGA-DK-A1A6-01 COSM1315591 c.8814G>A p.Q2938Q Substitution - coding silent 23:53551142-53551142 - TCGA-BS-A0UF-01 COSM281812 c.6229C>T p.R2077W Substitution - Missense 23:53568759-53568759 - ESCC_4 COSM5649967 c.13080_13082delACT p.L4362delL Deletion - In frame 23:53533352-53533354 - HCT116 COSM1682640 c.6073C>T p.R2025W Substitution - Missense 23:53569656-53569656 - TCGA-21-1070-01 COSM756919 c.10251C>T p.V3417V Substitution - coding silent 23:53547728-53547728 - GCT42 COSM1123162 c.6472G>A p.E2158K Substitution - Missense 23:53564720-53564720 - S01522 COSM4386980 c.1934G>A p.R645K Substitution - Missense 23:53616993-53616993 - T207 COSM4691591 c.5230A>G p.N1744D Substitution - Missense 23:53580906-53580906 - TCGA-FW-A3R5-06 COSM3914081 c.2762C>T p.S921F Substitution - Missense 23:53603482-53603482 - TCGA-06-1804-01 COSM3406481 c.5799T>C p.T1933T Substitution - coding silent 23:53573852-53573852 - 8665_CLM COSM5757553 c.4675A>G p.K1559E Substitution - Missense 23:53586849-53586849 - S00539 COSM5658970 c.11835delG p.Q3946fs*12 Deletion - Frameshift 23:53536640-53536640 - RKO COSM2968461 c.6853G>A p.D2285N Substitution - Missense 23:53565094-53565094 - 61 COSM5742298 c.6148C>T p.R2050W Substitution - Missense 23:53573914-53573914 - TCGA-JW-A5VL-01 COSM4847858 c.6592G>C p.E2198Q Substitution - Missense 23:53564600-53564600 - TCGA-IR-A3LK-01 COSM4816596 c.12841C>T p.R4281C Substitution - Missense 23:53533365-53533365 - TCGA-66-2763-01 COSM756928 c.12031G>T p.G4011W Substitution - Missense 23:53537662-53537662 - HCC19 COSM1625990 c.1310A>G p.D437G Substitution - Missense 23:53627812-53627812 - Gp5D COSM2968371 c.9511A>G p.T3171A Substitution - Missense 23:53549483-53549483 - RKO COSM2968462 c.6442G>A p.D2148N Substitution - Missense 23:53565094-53565094 - Pat_02_B COSM5878052 c.10886G>A p.R3629Q Substitution - Missense 23:53544595-53544595 - TCGA-JW-A5VL-01 COSM4847857 c.7003G>C p.E2335Q Substitution - Missense 23:53564600-53564600 - T2944 COSM4691561 c.12334C>T p.R4112C Substitution - Missense 23:53536471-53536471 - TCGA-AP-A051-01 COSM1123182 c.6073G>A p.A2025T Substitution - Missense 23:53575179-53575179 - 2012-1348:2012-1317-T COSM4604180 c.11886G>C p.E3962D Substitution - Missense 23:53536589-53536589 - TCGA-CF-A27C-01 COSM1315599 c.2709C>G p.I903M Substitution - Missense 23:53604622-53604622 - TCGA-BG-A0M4-01 COSM1123222 c.3120A>G p.P1040P Substitution - coding silent 23:53600161-53600161 - OSCC-GB_01060111 COSM4882611 c.453G>A p.L151L Substitution - coding silent 23:53645362-53645362 - S00934 COSM5663008 c.12535G>C p.D4179H Substitution - Missense 23:53534164-53534164 - TCGA-BT-A0YX-01 COSM422538 c.7248G>A p.L2416L Substitution - coding silent 23:53560265-53560265 - T2940 COSM4691571 c.9244C>A p.L3082I Substitution - Missense 23:53549420-53549420 - 40 COSM4169974 c.5052G>T p.R1684S Substitution - Missense 23:53584295-53584295 - 2011-2367:2012-1296-T COSM4604211 c.12285G>T p.E4095D Substitution - Missense 23:53535418-53535418 - COLO205 COSM612993 c.2034G>T p.T678T Substitution - coding silent 23:53615759-53615759 - SNUH_G26_S1 COSM4002322 c.9030A>G p.A3010A Substitution - coding silent 23:53550926-53550926 - PD24202a COSM5774299 c.11411G>A p.R3804Q Substitution - Missense 23:53542508-53542508 - LUAD-B00416 COSM355516 c.9393C>T p.T3131T Substitution - coding silent 23:53550761-53550761 - HCC96T COSM3708672 c.11626G>C p.V3876L Substitution - Missense 23:53538377-53538377 - CHC892T COSM4796682 c.9781G>A p.A3261T Substitution - Missense 23:53548198-53548198 - TCGA-EI-6882-01 COSM2968374 c.9068G>A p.R3023H Substitution - Missense 23:53550756-53550756 - LUAD-B00416 COSM355519 c.861A>G p.L287L Substitution - coding silent 23:53630936-53630936 - OSCC-GB_00540111 COSM4889546 c.11884C>G p.H3962D Substitution - Missense 23:53538449-53538449 - TCGA-A3-3374-01 COSM1497256 c.13027A>T p.N4343Y Substitution - Missense 23:53533407-53533407 - TCGA-DD-A3A9-01 COSM4920859 c.12148C>G p.L4050V Substitution - Missense 23:53536200-53536200 - TCGA-A8-A09A-01 COSM457757 c.1805G>C p.G602A Substitution - Missense 23:53617122-53617122 - HCC1187 COSM23117 c.1442G>A p.R481K Substitution - Missense 23:53627457-53627457 - TCGA-13-0886-01 COSM71123 c.4507T>A p.S1503T Substitution - Missense 23:53585095-53585095 - TCGA-B7-5816-01 COSM191513 c.6729C>T p.D2243D Substitution - coding silent 23:53562895-53562895 - TCGA-AP-A056-01 COSM1123212 c.4303G>T p.E1435* Substitution - Nonsense 23:53589705-53589705 - YULLON COSM1714993 c.12818_12819CC>TT p.S4273F Substitution - Missense 23:53534528-53534529 - TCGA-F4-6703-01 COSM5831305 c.1673-3delT p.? Unknown 23:53617449-53617449 - YUSMI COSM5412850 c.9467G>A p.G3156E Substitution - Missense 23:53550687-53550687 - CSCC-27-T COSM4513271 c.9321C>T p.L3107L Substitution - coding silent 23:53550965-53550965 - TCGA-A2-A3XT-01 COSM3845048 c.9634G>A p.V3212I Substitution - Missense 23:53549030-53549030 - TCGA-AP-A059-01 COSM1123160 c.6512T>C p.V2171A Substitution - Missense 23:53564680-53564680 - TCGA-BS-A0UV-01 COSM1123184 c.5711G>A p.G1904E Substitution - Missense 23:53580836-53580836 - SWE-54A COSM1178530 c.850A>G p.I284V Substitution - Missense 23:53630947-53630947 - CX-1 COSM1682632 c.10565A>C p.Y3522S Substitution - Missense 23:53546456-53546456 - LS411 COSM2968637 c.692A>G p.K231R Substitution - Missense 23:53631568-53631568 - TCGA-B0-4837-01 COSM3364052 c.8577A>T p.T2859T Substitution - coding silent 23:53552811-53552811 - PT38 COSM3562391 c.4018C>T p.R1340C Substitution - Missense 23:53589579-53589579 - TCGA-GM-A2D9-01 COSM3845054 c.6838C>G p.Q2280E Substitution - Missense 23:53562200-53562200 - pfg144T COSM4755418 c.12645G>C p.M4215I Substitution - Missense 23:53535388-53535388 - OSCC-GB_01060111 COSM4882612 c.453G>A p.L151L Substitution - coding silent 23:53645362-53645362 - TCGA-AP-A05N-01 COSM1123179 c.5916A>G p.L1972L Substitution - coding silent 23:53569813-53569813 - TCGA-DC-5869-01 COSM1570125 c.5359C>T p.R1787W Substitution - Missense 23:53583719-53583719 - SNU-175 COSM1123097 c.11338C>T p.R3780C Substitution - Missense 23:53543882-53543882 - sysucc-1163T COSM5459518 c.9092A>C p.Q3031P Substitution - Missense 23:53550732-53550732 - pfg173T COSM4755428 c.6643C>A p.L2215I Substitution - Missense 23:53568756-53568756 - 61 COSM5742293 c.12247G>T p.G4083W Substitution - Missense 23:53535456-53535456 - Pat_54_A COSM3562373 c.9152A>G p.H3051R Substitution - Missense 23:53550672-53550672 - TCGA-D1-A16X-01 COSM1123095 c.11382G>A p.S3794S Substitution - coding silent 23:53542537-53542537 - TCGA-DS-A1OC-01 COSM1294589 c.9448G>C p.G3150R Substitution - Missense 23:53550706-53550706 - TCGA-BR-A4CS-01 COSM4110175 c.6622G>A p.E2208K Substitution - Missense 23:53563818-53563818 - TCGA-66-2800-01 COSM756884 c.637G>A p.E213K Substitution - Missense 23:53632495-53632495 - 041T COSM1729600 c.10141A>T p.S3381C Substitution - Missense 23:53548168-53548168 - TCGA-AP-A056-01 COSM1123194 c.5339G>A p.R1780H Substitution - Missense 23:53583739-53583739 - TCGA-D1-A103-01 COSM1123080 c.11688G>T p.E3896D Substitution - Missense 23:53537675-53537675 - TCGA-BS-A0UJ-01 COSM1123108 c.10531A>G p.K3511E Substitution - Missense 23:53546490-53546490 - NB-0038 COSM1285459 c.9146G>C p.S3049T Substitution - Missense 23:53550678-53550678 - TCGA-B5-A11N-01 COSM1123089 c.11649C>T p.V3883V Substitution - coding silent 23:53539064-53539064 - Pat_08_B COSM5878056 c.6906_6908delGGA p.E2303delE Deletion - In frame 23:53562130-53562132 - LUAD-S01405 COSM404565 c.2284A>G p.I762V Substitution - Missense 23:53608887-53608887 - TCGA-AC-A23H-01 COSM3845061 c.5397G>C p.K1799N Substitution - Missense 23:53583681-53583681 - TCGA-DY-A1DF-01 COSM1570123 c.4421C>G p.A1474G Substitution - Missense 23:53589587-53589587 - TCGA-AP-A0LM-01 COSM1123138 c.8195C>A p.S2732Y Substitution - Missense 23:53552863-53552863 - TCGA-B5-A11E-01 COSM1123073 c.12227C>A p.P4076H Substitution - Missense 23:53536578-53536578 - PD4934a COSM161636 c.456A>G p.G152G Substitution - coding silent 23:53645359-53645359 - TCGA-AP-A051-01 COSM1123253 c.277C>T p.L93F Substitution - Missense 23:53647442-53647442 - YURUS COSM1714995 c.12703C>T p.P4235S Substitution - Missense 23:53534644-53534644 - PD3890a COSM4809958 c.5321C>T p.T1774I Substitution - Missense 23:53583757-53583757 - YUROG COSM5412856 c.4660C>T p.L1554F Substitution - Missense 23:53586864-53586864 - YUKAT COSM5412861 c.2146C>T p.P716S Substitution - Missense 23:53614649-53614649 - S00934 COSM5663007 c.12865G>C p.D4289H Substitution - Missense 23:53534164-53534164 - pfg108T COSM4755439 c.1586G>A p.R529Q Substitution - Missense 23:53625162-53625162 - CHC1556T COSM4787713 c.11127T>A p.S3709S Substitution - coding silent 23:53544684-53544684 - TCGA-BH-A18P-01 COSM457754 c.1847G>T p.R616L Substitution - Missense 23:53617080-53617080 - TCGA-IR-A3LK-01 COSM4816423 c.7497C>G p.F2499L Substitution - Missense 23:53561766-53561766 - 2011-2260:2012-1319-T COSM4604234 c.12564G>T p.Q4188H Substitution - Missense 23:53534135-53534135 - pfg005T COSM4755427 c.6639C>A p.D2213E Substitution - Missense 23:53563801-53563801 - TCGA-B7-5816-01 COSM4110189 c.2517A>C p.K839N Substitution - Missense 23:53604814-53604814 - CRC-19T COSM5482343 c.9706-5G>A p.? Unknown 23:53548278-53548278 - SNU-C2B COSM1123136 c.8510C>T p.P2837L Substitution - Missense 23:53552352-53552352 - TCGA-AP-A056-01 COSM1123081 c.11993G>A p.R3998H Substitution - Missense 23:53538340-53538340 - PT52 COSM5941141 c.5495C>T p.P1832L Substitution - Missense 23:53575767-53575767 - CSCC-38-T COSM4461717 c.11854C>T p.L3952L Substitution - coding silent 23:53536621-53536621 - TCGA-BR-8487-01 COSM4110193 c.1554C>T p.A518A Substitution - coding silent 23:53625194-53625194 - SNU-175 COSM2968382 c.8663C>T p.A2888V Substitution - Missense 23:53551369-53551369 - TCGA-BS-A0UF-01 COSM1123226 c.3001A>G p.M1001V Substitution - Missense 23:53600280-53600280 - OSCC-GB_00830111 COSM4506917 c.6925C>T p.Q2309* Substitution - Nonsense 23:53562113-53562113 - TCGA-MK-A4N7-01 COSM2968349 c.10221C>T p.S3407S Substitution - coding silent 23:53548088-53548088 - LUAD-B02216 COSM356327 c.797G>C p.G266A Substitution - Missense 23:53631000-53631000 - TCGA-AZ-6598-01 COSM1468593 c.9275A>G p.E3092G Substitution - Missense 23:53551011-53551011 - SNU-175 COSM2968381 c.8993C>T p.A2998V Substitution - Missense 23:53551369-53551369 - CSCC-27-T COSM4490934 c.3715C>T p.L1239L Substitution - coding silent 23:53593390-53593390 - S02237 COSM5676668 c.11536C>A p.L3846M Substitution - Missense 23:53539753-53539753 - P04-2740 COSM244976 c.10883G>A p.R3628H Substitution - Missense 23:53544598-53544598 - TCGA-66-2763-01 COSM756929 c.11701G>T p.G3901W Substitution - Missense 23:53537662-53537662 - ACINAR06 COSM1734862 c.4425T>A p.D1475E Substitution - Missense 23:53589583-53589583 - HCT116 COSM2968568 c.3180C>T p.G1060G Substitution - coding silent 23:53595387-53595387 - 273T COSM1727383 c.6880G>A p.G2294S Substitution - Missense 23:53565067-53565067 - T3670 COSM4691592 c.3239G>A p.R1080H Substitution - Missense 23:53595328-53595328 - B59 COSM1757282 c.3538G>A p.V1180I Substitution - Missense 23:53592421-53592421 - T3225 COSM4691575 c.8908A>G p.S2970G Substitution - Missense 23:53551048-53551048 - TCGA-BS-A0UV-01 COSM1123204 c.4634C>T p.A1545V Substitution - Missense 23:53586890-53586890 - TCGA-AX-A0J0-01 COSM1123248 c.980C>A p.S327Y Substitution - Missense 23:53628886-53628886 - SWE-8 COSM1178734 c.2688C>T p.L896L Substitution - coding silent 23:53604643-53604643 - TCGA-HU-8602-01 COSM1123122 c.9763C>T p.R3255W Substitution - Missense 23:53548216-53548216 - S02139 COSM5674738 c.6482G>T p.G2161V Substitution - Missense 23:53569658-53569658 - TCGA-BH-A0B0-01 COSM457750 c.7199G>A p.R2400Q Substitution - Missense 23:53562836-53562836 - TCGA-D1-A103-01 COSM1123151 c.7425C>T p.N2475N Substitution - coding silent 23:53561838-53561838 - TCGA-AP-A051-01 COSM1123241 c.1666C>A p.L556I Substitution - Missense 23:53624601-53624601 - PA285 COSM1163764 c.7471_7472delTT p.F2491fs*2 Deletion - Frameshift 23:53559386-53559387 - Pat_41_B COSM5878049 c.11533C>T p.P3845S Substitution - Missense 23:53539756-53539756 - CSCC-38-T COSM4446202 c.1672+3_1672+4AA>GG p.? Unknown 23:53624591-53624592 - PT45 COSM5927956 c.2659G>C p.A887P Substitution - Missense 23:53604672-53604672 - TCGA-AA-3818-01 COSM270837 c.9191G>A p.R3064H Substitution - Missense 23:53549473-53549473 - 587306 COSM1210159 c.2738G>T p.G913V Substitution - Missense 23:53604593-53604593 - LUAD_E00522 COSM388781 c.4453G>A p.D1485N Substitution - Missense 23:53585149-53585149 - TCGA-B5-A0JZ-01 COSM1123094 c.11109C>A p.D3703E Substitution - Missense 23:53542480-53542480 - CSCC-31-T COSM4565408 c.2084_2085CC>TT p.P695L Substitution - Missense 23:53614710-53614711 - TCGA-G4-6302-01 COSM3694649 c.5137A>G p.K1713E Substitution - Missense 23:53584210-53584210 - SJTALL005 COSM1468621 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - BD124T COSM5494282 c.7748A>G p.Q2583R Substitution - Missense 23:53558656-53558656 - 587284 COSM1210167 c.12704C>T p.P4235L Substitution - Missense 23:53534643-53534643 - S00539 COSM5658971 c.444C>A p.I148I Substitution - coding silent 23:53645371-53645371 - Mx34 COSM50797 c.9470G>A p.R3157H Substitution - Missense 23:53549194-53549194 - TCGA-46-3769-01 COSM756882 c.516A>T p.G172G Substitution - coding silent 23:53634287-53634287 - TCGA-AP-A0LM-01 COSM1123137 c.8525C>A p.S2842Y Substitution - Missense 23:53552863-53552863 - TCGA-D9-A3Z1-06 COSM3562408 c.1954C>T p.L652F Substitution - Missense 23:53616973-53616973 - TCGA-A7-A3J1-01 COSM3845060 c.5597C>T p.T1866M Substitution - Missense 23:53575665-53575665 - TCGA-D9-A6EC-06 COSM4400021 c.6297T>C p.S2099S Substitution - coding silent 23:53573765-53573765 - sysucc-311T COSM5467902 c.5305+9C>T p.? Unknown 23:53580822-53580822 - CSCC-27-T COSM4564189 c.10547_10548CC>TT p.A3516V Substitution - Missense 23:53547761-53547762 - TCGA-AP-A0LG-01 COSM1123189 c.5258A>G p.N1753S Substitution - Missense 23:53580878-53580878 - HCC2998 COSM1682626 c.11026C>T p.R3676W Substitution - Missense 23:53543864-53543864 - HCC2998 COSM2968608 c.1540T>C p.F514L Substitution - Missense 23:53625208-53625208 - TCGA-CC-A123-01 COSM4915310 c.7070A>G p.E2357G Substitution - Missense 23:53561782-53561782 - 471 COSM1682628 c.10966C>T p.R3656W Substitution - Missense 23:53543924-53543924 - TCGA-FS-A4FB-06 COSM3562372 c.9482A>G p.H3161R Substitution - Missense 23:53550672-53550672 - TCGA-AA-3837-01 COSM271658 c.4790A>G p.E1597G Substitution - Missense 23:53583877-53583877 - TCGA-43-5668-01 COSM756875 c.145T>C p.C49R Substitution - Missense 23:53647574-53647574 - TCGA-D8-A27P-01 COSM1491085 c.12380G>A p.R4127H Substitution - Missense 23:53534637-53534637 - CSCC-31-T COSM4492200 c.3523C>T p.R1175C Substitution - Missense 23:53592436-53592436 - 2492700 COSM5715750 c.8820C>T p.S2940S Substitution - coding silent 23:53552372-53552372 - ESO-640 COSM1254540 c.1018A>G p.T340A Substitution - Missense 23:53628848-53628848 - sysucc-1116T COSM5483143 c.3251G>A p.S1084N Substitution - Missense 23:53595316-53595316 - TCGA-14-1823-01 COSM3406479 c.7081G>A p.G2361R Substitution - Missense 23:53563770-53563770 - T578 COSM4691559 c.12690C>A p.F4230L Substitution - Missense 23:53534657-53534657 - 8066852 COSM1210157 c.148G>A p.E50K Substitution - Missense 23:53647571-53647571 - MO_1316 COSM5549200 c.6992C>A p.A2331D Substitution - Missense 23:53564611-53564611 - TCGA-AP-A056-01 COSM1123173 c.6212G>A p.G2071D Substitution - Missense 23:53568776-53568776 - 07-058 COSM3736501 c.12821A>C p.N4274T Substitution - Missense 23:53534526-53534526 - PD4112a COSM161633 c.8093C>A p.T2698K Substitution - Missense 23:53554668-53554668 - TCGA-46-6025-01 COSM756913 c.8839G>T p.D2947Y Substitution - Missense 23:53551117-53551117 - 179T COSM1123161 c.6883G>A p.E2295K Substitution - Missense 23:53564720-53564720 - TCGA-D1-A103-01 COSM1123200 c.5246G>T p.G1749V Substitution - Missense 23:53583832-53583832 - TCGA-D1-A1NU-01 COSM1123225 c.2783C>T p.S928L Substitution - Missense 23:53600167-53600167 - 587220 COSM1210158 c.148G>A p.E50K Substitution - Missense 23:53647571-53647571 - TCGA-CZ-4862-01 COSM1468592 c.9005T>A p.L3002Q Substitution - Missense 23:53550951-53550951 - M14 COSM1682636 c.9890C>T p.S3297F Substitution - Missense 23:53548089-53548089 - TCGA-EB-A3XC-01 COSM3562386 c.5531C>T p.S1844L Substitution - Missense 23:53581016-53581016 - TCGA-BR-6452-01 COSM4110195 c.1308T>C p.V436V Substitution - coding silent 23:53627814-53627814 - T407 COSM4691599 c.273G>A p.M91I Substitution - Missense 23:53647446-53647446 - CHC1745T COSM4805848 c.10702G>T p.G3568C Substitution - Missense 23:53545045-53545045 - TCGA-EK-A3GK-01 COSM4853311 c.1686G>A p.V562V Substitution - coding silent 23:53617433-53617433 - TCGA-DY-A1DF-01 COSM1570124 c.4010C>G p.A1337G Substitution - Missense 23:53589587-53589587 - TCGA-AP-A056-01 COSM1123213 c.3892G>T p.E1298* Substitution - Nonsense 23:53589705-53589705 - T1154 COSM4691577 c.8213T>C p.V2738A Substitution - Missense 23:53552845-53552845 - HCC107T COSM1625986 c.7049G>T p.R2350L Substitution - Missense 23:53561803-53561803 - TCGA-AP-A056-01 COSM1123145 c.7972C>T p.L2658F Substitution - Missense 23:53559004-53559004 - TCGA-D3-A51T-06 COSM3562355 c.11388C>T p.S3796S Substitution - coding silent 23:53538995-53538995 - TCGA-AZ-6598-01 COSM1468594 c.8945A>G p.E2982G Substitution - Missense 23:53551011-53551011 - sysucc-1512T COSM5450822 c.1071A>G p.G357G Substitution - coding silent 23:53628795-53628795 - SJBALL021521_D1 COSM4994154 c.8041C>A p.P2681T Substitution - Missense 23:53554720-53554720 - TCGA-43-2578-01 COSM756925 c.10265C>A p.T3422N Substitution - Missense 23:53547714-53547714 - TCGA-A6-6780-01 COSM1468573 c.11726C>T p.A3909V Substitution - Missense 23:53538987-53538987 - RK007_C01 COSM1636573 c.7959A>C p.E2653D Substitution - Missense 23:53559017-53559017 - RKO COSM2968509 c.5391A>G p.E1797E Substitution - coding silent 23:53583687-53583687 - PTC-28C COSM4156911 c.3523C>G p.R1175G Substitution - Missense 23:53592436-53592436 - TCGA-BL-A3JM-01 COSM1315600 c.402C>T p.V134V Substitution - coding silent 23:53645413-53645413 - TCGA-66-2767-01 COSM756886 c.1990G>A p.D664N Substitution - Missense 23:53615803-53615803 - ESO-137 COSM1254538 c.676A>G p.I226V Substitution - Missense 23:53631584-53631584 - 3844_T COSM3965375 c.5754C>T p.G1918G Substitution - coding silent 23:53573897-53573897 - I2L-P19Tb-Tumor-Biopsy COSM5367076 c.11676C>T p.R3892R Substitution - coding silent 23:53537687-53537687 - I2L-P19Ta-Tumor-Organoid COSM5367057 c.2014A>C p.T672P Substitution - Missense 23:53615779-53615779 - S02384 COSM5698691 c.3118C>A p.P1040T Substitution - Missense 23:53600163-53600163 - TCGA-AA-A00N-01 COSM275508 c.4815C>T p.I1605I Substitution - coding silent 23:53583852-53583852 - S00934 COSM5663009 c.11846C>T p.P3949L Substitution - Missense 23:53538867-53538867 - TCGA-LL-A5YN-01 COSM4391463 c.2740C>G p.Q914E Substitution - Missense 23:53604591-53604591 - TCGA-AP-A051-01 COSM1123183 c.5662G>A p.A1888T Substitution - Missense 23:53575179-53575179 - 2011-2297:2012-323-T COSM4605645 c.5413A>G p.I1805V Substitution - Missense 23:53576960-53576960 - SNU-C4 COSM4654565 c.10263G>A p.S3421S Substitution - coding silent 23:53547716-53547716 - 40M COSM5585442 c.10373C>T p.S3458F Substitution - Missense 23:53547936-53547936 - PD24307a COSM5774405 c.4379G>A p.R1460H Substitution - Missense 23:53589629-53589629 - TCGA-BR-7707-01 COSM4110166 c.7403G>A p.R2468H Substitution - Missense 23:53559455-53559455 - TCGA-AN-A046-01 COSM3845049 c.9358G>A p.A3120T Substitution - Missense 23:53550928-53550928 - HCC122T COSM5808595 c.3093-2A>G p.? Unknown 23:53593603-53593603 - TCGA-61-1900-01 COSM1331791 c.391G>T p.V131L Substitution - Missense 23:53645424-53645424 - 169 COSM3729787 c.10845G>T p.R3615S Substitution - Missense 23:53544636-53544636 - OSCC-GB_00830111 COSM4506916 c.7336C>T p.Q2446* Substitution - Nonsense 23:53562113-53562113 - S01023 COSM5666906 c.927G>A p.L309L Substitution - coding silent 23:53629552-53629552 - TCGA-RP-A695-06 COSM4896077 c.10379A>G p.K3460R Substitution - Missense 23:53546753-53546753 - PD24212a COSM5781059 c.10706A>C p.K3569T Substitution - Missense 23:53545041-53545041 - TCGA-AX-A05Z-01 COSM1123239 c.1777G>T p.D593Y Substitution - Missense 23:53617342-53617342 - TCGA-D1-A103-01 COSM1123258 c.117G>A p.Q39Q Substitution - coding silent 23:53648239-53648239 - TCGA-A3-3316-01 COSM1497253 c.7030C>T p.R2344* Substitution - Nonsense 23:53561822-53561822 - TCGA-BP-4991-01 COSM488477 c.4868G>T p.R1623L Substitution - Missense 23:53585145-53585145 - 587232 COSM1210178 c.7427T>G p.V2476G Substitution - Missense 23:53559431-53559431 - TCGA-EB-A3XD-01 COSM3562350 c.12114C>T p.S4038S Substitution - coding silent 23:53537579-53537579 - XHDG32 COSM4769390 c.6334G>T p.V2112F Substitution - Missense 23:53569806-53569806 - TCGA-EK-A3GK-01 COSM4853310 c.1686G>A p.V562V Substitution - coding silent 23:53617433-53617433 - S02255 COSM5681136 c.8284G>T p.G2762C Substitution - Missense 23:53552774-53552774 - TCGA-BR-8078-01 COSM4110145 c.11669A>G p.H3890R Substitution - Missense 23:53539044-53539044 - TCGA-04-1356-01 COSM120009 c.6140G>A p.S2047N Substitution - Missense 23:53568848-53568848 - PD4084a COSM161632 c.4710C>A p.S1570R Substitution - Missense 23:53584226-53584226 - SA212 COSM213911 c.6825G>T p.E2275D Substitution - Missense 23:53562213-53562213 - HCT15 COSM1682638 c.9316G>A p.A3106T Substitution - Missense 23:53549348-53549348 - RK095_C01 COSM3701869 c.12811T>C p.Y4271H Substitution - Missense 23:53534536-53534536 - TCGA-29-1777-01 COSM1331797 c.9361C>A p.Q3121K Substitution - Missense 23:53549303-53549303 - CCK81 COSM2968248 c.12775A>G p.I4259V Substitution - Missense 23:53534572-53534572 - MDA-MB-435 COSM1682635 c.10220C>T p.S3407F Substitution - Missense 23:53548089-53548089 - TCGA-ER-A19S-06 COSM3562405 c.1960G>A p.D654N Substitution - Missense 23:53615833-53615833 - TCGA-BS-A0UV-01 COSM1123208 c.4590C>A p.I1530I Substitution - coding silent 23:53588406-53588406 - TCGA-EI-6882-01 COSM2968373 c.9398G>A p.R3133H Substitution - Missense 23:53550756-53550756 - SNU-C2B COSM2968487 c.6005A>T p.D2002V Substitution - Missense 23:53575668-53575668 - EGC15 COSM4110149 c.10828C>T p.R3610W Substitution - Missense 23:53546523-53546523 - SNU-C4 COSM4654564 c.10593G>A p.S3531S Substitution - coding silent 23:53547716-53547716 - AB COSM5414948 c.1728C>A p.L576L Substitution - coding silent 23:53617391-53617391 - TCGA-AP-A059-01 COSM1123109 c.10716G>A p.V3572V Substitution - coding silent 23:53546746-53546746 - TCGA-HM-A3JK-01 COSM4854892 c.4540A>G p.I1514V Substitution - Missense 23:53588456-53588456 - ME050T COSM230824 c.754G>A p.D252N Substitution - Missense 23:53631422-53631422 - PT45 COSM5927955 c.2659G>C p.A887P Substitution - Missense 23:53604672-53604672 - TCGA-60-2698-01 COSM756906 c.8177C>G p.S2726* Substitution - Nonsense 23:53557411-53557411 - STC248 COSM5064761 c.5295G>A p.M1765I Substitution - Missense 23:53583783-53583783 - TCGA-BS-A0UF-01 COSM1123165 c.6640C>T p.R2214W Substitution - Missense 23:53568759-53568759 - TCGA-MK-A4N7-01 COSM2968350 c.9891C>T p.S3297S Substitution - coding silent 23:53548088-53548088 - NB-0038 COSM1285458 c.9476G>C p.S3159T Substitution - Missense 23:53550678-53550678 - PD4934a COSM4809521 c.456A>G p.G152G Substitution - coding silent 23:53645359-53645359 - ESCC-F51 COSM5047980 c.3655C>A p.P1219T Substitution - Missense 23:53591029-53591029 - MS4 COSM1165433 c.11888G>A p.R3963H Substitution - Missense 23:53538445-53538445 - LUAD-5V8LT COSM403174 c.12659G>C p.R4220P Substitution - Missense 23:53534688-53534688 - KYSE180 COSM756913 c.8839G>T p.D2947Y Substitution - Missense 23:53551117-53551117 - 35M COSM5581337 c.4836C>T p.S1612S Substitution - coding silent 23:53585177-53585177 - 2492703 COSM5715751 c.8490C>T p.S2830S Substitution - coding silent 23:53552372-53552372 - ATL027 COSM5711706 c.12067C>T p.R4023C Substitution - Missense 23:53537626-53537626 - 53M COSM5594697 c.1005C>T p.V335V Substitution - coding silent 23:53628861-53628861 - TCGA-D1-A17A-01 COSM1123169 c.6224T>G p.I2075S Substitution - Missense 23:53568764-53568764 - TCGA-D3-A1QB-06 COSM3562392 c.4162C>T p.P1388S Substitution - Missense 23:53590433-53590433 - S00831 COSM5660704 c.1537A>T p.N513Y Substitution - Missense 23:53625211-53625211 - H1299 COSM1193510 c.11546C>T p.A3849V Substitution - Missense 23:53538837-53538837 - CSCC-44-T COSM4500379 c.5234C>T p.P1745L Substitution - Missense 23:53580902-53580902 - sysucc-783T COSM5485170 c.2880C>T p.A960A Substitution - coding silent 23:53595276-53595276 - HCT8 COSM4635812 c.9747G>T p.E3249D Substitution - Missense 23:53549247-53549247 - SNU-175 COSM1123098 c.11008C>T p.R3670C Substitution - Missense 23:53543882-53543882 - TCGA-B5-A0JY-01 COSM1123255 c.255A>C p.E85D Substitution - Missense 23:53647464-53647464 - TCGA-B5-A11N-01 COSM1123090 c.11319C>T p.V3773V Substitution - coding silent 23:53539064-53539064 - GC_351T-GC_351N COSM4774018 c.5986C>T p.R1996C Substitution - Missense 23:53575687-53575687 - HDC101 COSM4636203 c.6970G>A p.E2324K Substitution - Missense 23:53564633-53564633 - ESCC_BICR_060T COSM5435210 c.12224A>G p.N4075S Substitution - Missense 23:53536581-53536581 - TCGA-IR-A3LK-01 COSM4816424 c.7086C>G p.F2362L Substitution - Missense 23:53561766-53561766 - PD2205a COSM28420 c.12411A>T p.L4137F Substitution - Missense 23:53534606-53534606 - TCGA-EB-A42Y-01 COSM3562365 c.10088A>G p.Q3363R Substitution - Missense 23:53547891-53547891 - TCGA-D3-A3C7-06 COSM3562367 c.9710T>A p.F3237Y Substitution - Missense 23:53548269-53548269 - HCC2998 COSM1682627 c.11296C>T p.R3766W Substitution - Missense 23:53543924-53543924 - ESCC_BICR_050T COSM488477 c.4868G>T p.R1623L Substitution - Missense 23:53585145-53585145 - B101 COSM1757277 c.9600C>T p.L3200L Substitution - coding silent 23:53549394-53549394 - Gp2D COSM2968242 c.12940delC p.L4314fs*4 Deletion - Frameshift 23:53534089-53534089 - TCGA-AP-A051-01 COSM1123175 c.6109G>A p.A2037T Substitution - Missense 23:53569620-53569620 - BCB307T COSM4950136 c.6121G>T p.A2041S Substitution - Missense 23:53568867-53568867 - 8067242 COSM3780516 c.12028G>A p.D4010N Substitution - Missense 23:53536447-53536447 - TCGA-CD-A4MG-01 COSM4110158 c.9860A>G p.N3287S Substitution - Missense 23:53548119-53548119 - TCGA-BS-A0UF-01 COSM1123124 c.9561G>T p.R3187S Substitution - Missense 23:53549103-53549103 - 8052570 COSM3390709 c.12812A>G p.Y4271C Substitution - Missense 23:53534535-53534535 - M14 COSM1682635 c.10220C>T p.S3407F Substitution - Missense 23:53548089-53548089 - TCGA-61-1907-01 COSM1331799 c.11987A>T p.Y3996F Substitution - Missense 23:53536488-53536488 - 2011-2373:2012-1301-T COSM457740 c.13060G>C p.E4354Q Substitution - Missense 23:53533374-53533374 - TCGA-C4-A0F6-01 COSM422535 c.5865A>G p.A1955A Substitution - coding silent 23:53576919-53576919 - PD4203a COSM161635 c.8089G>C p.E2697Q Substitution - Missense 23:53554672-53554672 - 8066852 COSM1210158 c.148G>A p.E50K Substitution - Missense 23:53647571-53647571 - 23 COSM5015752 c.452T>C p.L151P Substitution - Missense 23:53645363-53645363 - CSCC-5-T COSM4451433 c.11828A>G p.E3943G Substitution - Missense 23:53536647-53536647 - BK0020 COSM4186260 c.10478C>A p.T3493N Substitution - Missense 23:53547831-53547831 - 2492702 COSM5715750 c.8820C>T p.S2940S Substitution - coding silent 23:53552372-53552372 - OSCC-GB_00670111 COSM4883909 c.1489+1G>T p.? Unknown 23:53627409-53627409 - OSCC-GB_01060111 COSM4882831 c.6607C>A p.Q2203K Substitution - Missense 23:53564585-53564585 - GC_351T-GC_351N COSM4774019 c.5575C>T p.R1859C Substitution - Missense 23:53575687-53575687 - ICC009T COSM5823560 c.6201C>T p.T2067T Substitution - coding silent 23:53568787-53568787 - TCGA-EB-A3XC-01 COSM3562387 c.5120C>T p.S1707L Substitution - Missense 23:53581016-53581016 - Gp5D COSM2968566 c.2883G>A p.A961A Substitution - coding silent 23:53595273-53595273 - YUZINO COSM1715000 c.6610G>A p.E2204K Substitution - Missense 23:53564582-53564582 - DM851T COSM673992 c.808C>A p.H270N Substitution - Missense 23:53630989-53630989 - TCGA-D8-A27P-01 COSM1491084 c.12710G>A p.R4237H Substitution - Missense 23:53534637-53534637 - pfg103T COSM4755431 c.5720A>G p.K1907R Substitution - Missense 23:53573931-53573931 - TCGA-DA-A1HW-06 COSM3562409 c.1434G>A p.K478K Substitution - coding silent 23:53627465-53627465 - TCGA-B5-A11G-01 COSM1123088 c.11438T>C p.L3813S Substitution - Missense 23:53538945-53538945 - SNUH_G76_S1 COSM4419895 c.2109A>G p.S703S Substitution - coding silent 23:53614686-53614686 - 2492721 COSM5723309 c.8477C>T p.S2826F Substitution - Missense 23:53554650-53554650 - CSCC-41-T COSM4509334 c.7630C>T p.L2544L Substitution - coding silent 23:53558774-53558774 - Pat_41_B COSM5878048 c.12488C>T p.S4163F Substitution - Missense 23:53534529-53534529 - TCGA-BQ-5875-01 COSM3992539 c.11675G>A p.R3892H Substitution - Missense 23:53537688-53537688 - SNU-175 COSM2968349 c.10221C>T p.S3407S Substitution - coding silent 23:53548088-53548088 - CHC892T COSM4796436 c.6114G>A p.R2038R Substitution - coding silent 23:53568874-53568874 - PCA78-2 COSM5415754 c.3773A>G p.N1258S Substitution - Missense 23:53592597-53592597 - TCGA-DK-A1A6-01 COSM1315593 c.8781G>C p.Q2927H Substitution - Missense 23:53551175-53551175 - TCGA-DU-7012-01 COSM3973739 c.1416G>A p.P472P Substitution - coding silent 23:53627483-53627483 - TCGA-A8-A09I-01 COSM457740 c.13060G>C p.E4354Q Substitution - Missense 23:53533374-53533374 - TCGA-AP-A051-01 COSM1123242 c.1666C>A p.L556I Substitution - Missense 23:53624601-53624601 - SW948 COSM2968412 c.7630G>A p.G2544R Substitution - Missense 23:53560294-53560294 - TCGA-IR-A3LI-01 COSM4846212 c.8287G>A p.D2763N Substitution - Missense 23:53552771-53552771 - SJOS004_D COSM5023548 c.3451C>G p.H1151D Substitution - Missense 23:53594551-53594551 - Pat_66_A COSM5878059 c.3935G>A p.R1312H Substitution - Missense 23:53592435-53592435 - TCGA-B0-4713-01 COSM3364165 c.8704C>A p.P2902T Substitution - Missense 23:53551328-53551328 - TCGA-DD-A4NQ-01 COSM4941031 c.1105G>A p.A369T Substitution - Missense 23:53628761-53628761 - Gp2D COSM2968566 c.2883G>A p.A961A Substitution - coding silent 23:53595273-53595273 - CHC1556T COSM4787714 c.10797T>A p.S3599S Substitution - coding silent 23:53544684-53544684 - HCC058T COSM5805543 c.5100A>T p.L1700L Substitution - coding silent 23:53584247-53584247 - TCGA-AP-A0LM-01 COSM1123127 c.9549C>T p.H3183H Substitution - coding silent 23:53549445-53549445 - TCGA-EE-A29M-06 COSM3562357 c.11192C>T p.P3731L Substitution - Missense 23:53539767-53539767 - TCGA-IR-A3LK-01 COSM4817901 c.995C>G p.T332R Substitution - Missense 23:53628871-53628871 - TCGA-AP-A059-01 COSM1123159 c.6923T>C p.V2308A Substitution - Missense 23:53564680-53564680 - ESO-137 COSM1254537 c.676A>G p.I226V Substitution - Missense 23:53631584-53631584 - T2458 COSM4691584 c.7241A>G p.E2414G Substitution - Missense 23:53562208-53562208 - TCGA-A6-5665-01 COSM1468572 c.11657T>C p.V3886A Substitution - Missense 23:53538346-53538346 - TCGA-B0-4837-01 COSM3364053 c.8247A>T p.T2749T Substitution - coding silent 23:53552811-53552811 - TCGA-DD-A73F-01 COSM4935433 c.9292C>A p.R3098R Substitution - coding silent 23:53550994-53550994 - Pat_24_B COSM5878054 c.7205T>A p.L2402H Substitution - Missense 23:53560308-53560308 - Gp5D COSM2968243 c.12610delC p.L4204fs*4 Deletion - Frameshift 23:53534089-53534089 - S02290 COSM5686879 c.2441A>T p.D814V Substitution - Missense 23:53607578-53607578 - TCGA-D1-A16X-01 COSM1123057 c.13088C>T p.A4363V Substitution - Missense 23:53533346-53533346 - TCGA-C4-A0F6-01 COSM422536 c.5454A>G p.A1818A Substitution - coding silent 23:53576919-53576919 - CRC-19T COSM5482342 c.10036-5G>A p.? Unknown 23:53548278-53548278 - TCGA-BR-4357-01 COSM4110198 c.1042G>A p.D348N Substitution - Missense 23:53628824-53628824 - H1299 COSM1193509 c.11876C>T p.A3959V Substitution - Missense 23:53538837-53538837 - TCGA-BH-A2L8-01 COSM3845040 c.11048C>T p.T3683M Substitution - Missense 23:53543842-53543842 - sysucc-627T COSM5468124 c.10004G>A p.R3335Q Substitution - Missense 23:53547975-53547975 - TCGA-AN-A046-01 COSM3845044 c.10252G>A p.V3418I Substitution - Missense 23:53547727-53547727 - BCB307T COSM4950135 c.6532G>T p.A2178S Substitution - Missense 23:53568867-53568867 - TCGA-BH-A1FM-01 COSM1491090 c.7450C>T p.R2484C Substitution - Missense 23:53561813-53561813 - TCGA-AX-A0J0-01 COSM1123247 c.980C>A p.S327Y Substitution - Missense 23:53628886-53628886 - T3262 COSM4691565 c.11624C>T p.A3875V Substitution - Missense 23:53539665-53539665 - 2011-2367:2012-1296-T COSM4604210 c.12615G>T p.E4205D Substitution - Missense 23:53535418-53535418 - PD24212a COSM5781058 c.11036A>C p.K3679T Substitution - Missense 23:53545041-53545041 - E20 COSM1666207 c.6382A>C p.T2128P Substitution - Missense 23:53569758-53569758 - ESCC-F10 COSM5046683 c.10987G>C p.D3663H Substitution - Missense 23:53543903-53543903 - CHC1061T COSM250784 c.7866C>G p.Y2622* Substitution - Nonsense 23:53554895-53554895 - LUAD-B00416 COSM355521 c.216G>A p.V72V Substitution - coding silent 23:53647503-53647503 - 471 COSM1682627 c.11296C>T p.R3766W Substitution - Missense 23:53543924-53543924 - TCGA-60-2720-01 COSM756895 c.3972G>T p.V1324V Substitution - coding silent 23:53589625-53589625 - TCGA-EW-A1IZ-01 COSM1491093 c.6906G>A p.E2302E Substitution - coding silent 23:53562132-53562132 - TCGA-FU-A3TX-01 COSM4849371 c.12037C>T p.R4013W Substitution - Missense 23:53537656-53537656 - TCGA-DD-A73F-01 COSM4935434 c.8962C>A p.R2988R Substitution - coding silent 23:53550994-53550994 - TCGA-F4-6703-01 COSM5831304 c.1673-3delT p.? Unknown 23:53617449-53617449 - SC_9037 COSM5558939 c.6303G>A p.L2101L Substitution - coding silent 23:53573759-53573759 - S02347 COSM5694401 c.2164G>T p.A722S Substitution - Missense 23:53614631-53614631 - D-11 COSM4766775 c.3182G>C p.R1061P Substitution - Missense 23:53595385-53595385 - TCGA-BS-A0UJ-01 COSM1123227 c.2970A>G p.S990S Substitution - coding silent 23:53602565-53602565 - LUAD-YINHD COSM388586 c.8109G>T p.K2703N Substitution - Missense 23:53558706-53558706 - CSCC-5-T COSM4451432 c.12158A>G p.E4053G Substitution - Missense 23:53536647-53536647 - TCGA-FW-A3R5-06 COSM3914077 c.4099C>T p.L1367F Substitution - Missense 23:53590496-53590496 - LUAD-F00057 COSM365530 c.6694+1G>T p.? Unknown 23:53563745-53563745 - HCC2998 COSM1682627 c.11296C>T p.R3766W Substitution - Missense 23:53543924-53543924 - 587234 COSM1210173 c.9014C>T p.A3005V Substitution - Missense 23:53551348-53551348 - 8052570 COSM3390710 c.12482A>G p.Y4161C Substitution - Missense 23:53534535-53534535 - Pat_40_A COSM5878061 c.3802C>T p.R1268* Substitution - Nonsense 23:53592568-53592568 - TCGA-AZ-4315-01 COSM1468617 c.725C>T p.S242F Substitution - Missense 23:53631451-53631451 - TCGA-D8-A1XK-01 COSM3845069 c.1116T>C p.D372D Substitution - coding silent 23:53628619-53628619 - T578 COSM4691560 c.12360C>A p.F4120L Substitution - Missense 23:53534657-53534657 - YUOTHO COSM5412848 c.9747G>A p.E3249E Substitution - coding silent 23:53549247-53549247 - TCGA-D9-A6EC-06 COSM4400022 c.5886T>C p.S1962S Substitution - coding silent 23:53573765-53573765 - CSCC-44-T COSM4500378 c.5645C>T p.P1882L Substitution - Missense 23:53580902-53580902 - CSCC-44-T COSM4564012 c.11576_11577TC>AT p.I3859N Substitution - Missense 23:53538426-53538427 - TCGA-EE-A3AE-06 COSM3914080 c.3496G>A p.D1166N Substitution - Missense 23:53592463-53592463 - 201 COSM3722118 c.4943T>C p.L1648P Substitution - Missense 23:53583724-53583724 - ESCC-184T COSM3940040 c.12445G>A p.E4149K Substitution - Missense 23:53536233-53536233 - LUAD-NYU739 COSM376328 c.6047T>A p.V2016E Substitution - Missense 23:53569682-53569682 - TCGA-EE-A3AF-06 COSM3562368 c.9793G>A p.E3265K Substitution - Missense 23:53549201-53549201 - TCGA-GV-A3JX-01 COSM1315595 c.3719G>C p.R1240T Substitution - Missense 23:53590465-53590465 - TCGA-BH-A0BZ-01 COSM457752 c.4158T>A p.D1386E Substitution - Missense 23:53590437-53590437 - 2217529 COSM4421639 c.11787C>T p.P3929P Substitution - coding silent 23:53537576-53537576 - TCGA-06-0876-01 COSM2152061 c.10551C>T p.A3517A Substitution - coding silent 23:53546470-53546470 - TCGA-B5-A11E-01 COSM1123129 c.9532C>T p.R3178W Substitution - Missense 23:53549462-53549462 - 2492721 COSM5723310 c.8111C>T p.S2704F Substitution - Missense 23:53554650-53554650 - TCGA-E2-A1II-01 COSM1491086 c.12542T>G p.F4181C Substitution - Missense 23:53535491-53535491 - ESCC-175T COSM3940045 c.10335T>G p.S3445S Substitution - coding silent 23:53546797-53546797 - TCGA-C5-A1MH-01 COSM4821043 c.6742G>A p.E2248K Substitution - Missense 23:53562882-53562882 - TCGA-BR-8487-01 COSM4110170 c.6962A>G p.D2321G Substitution - Missense 23:53561890-53561890 - 61 COSM3562365 c.10088A>G p.Q3363R Substitution - Missense 23:53547891-53547891 - RK181_C01 COSM3766997 c.7504G>A p.A2502T Substitution - Missense 23:53561759-53561759 - TCGA-D7-A4YV-01 COSM4110188 c.2625T>G p.A875A Substitution - coding silent 23:53604706-53604706 - 2011-2283:2012-316-T COSM4604683 c.2052A>G p.L684L Substitution - coding silent 23:53614743-53614743 - T3724 COSM4691594 c.2673T>G p.P891P Substitution - coding silent 23:53604658-53604658 - PM-3 COSM5619975 c.10480A>C p.T3494P Substitution - Missense 23:53547829-53547829 - YURUS COSM1714996 c.12373C>T p.P4125S Substitution - Missense 23:53534644-53534644 - PM-3 COSM5619976 c.10150A>C p.T3384P Substitution - Missense 23:53547829-53547829 - B101-Tumor COSM1757278 c.9270C>T p.L3090L Substitution - coding silent 23:53549394-53549394 - TCGA-BR-8487-01 COSM4110161 c.8437A>C p.R2813R Substitution - coding silent 23:53554690-53554690 - EWS502 COSM4589487 c.3084T>C p.A1028A Substitution - coding silent 23:53594507-53594507 - TCGA-C8-A27B-01 COSM1491094 c.2548T>G p.S850A Substitution - Missense 23:53604783-53604783 - CHC429T COSM250785 c.1813C>G p.P605A Substitution - Missense 23:53617114-53617114 - TCGA-B5-A11Y-01 COSM1123076 c.11843C>T p.A3948V Substitution - Missense 23:53536632-53536632 - TCGA-AG-A002-01 COSM261351 c.12650G>A p.R4217Q Substitution - Missense 23:53534049-53534049 - 90879 COSM329407 c.6760T>C p.S2254P Substitution - Missense 23:53565187-53565187 - TCGA-DK-A3IU-01 COSM3800673 c.9051G>C p.V3017V Substitution - coding silent 23:53551311-53551311 - TCGA-43-6143-01 COSM756914 c.9203A>G p.D3068G Substitution - Missense 23:53551083-53551083 - S00539 COSM5658969 c.12165delG p.Q4056fs*12 Deletion - Frameshift 23:53536640-53536640 - PD4203a COSM4810202 c.8455G>C p.E2819Q Substitution - Missense 23:53554672-53554672 - 587388 COSM1210171 c.12292C>T p.H4098Y Substitution - Missense 23:53536513-53536513 - TCGA-CM-6674-01 COSM1468595 c.7711C>T p.P2571S Substitution - Missense 23:53560213-53560213 - B101-Tumor COSM1757277 c.9600C>T p.L3200L Substitution - coding silent 23:53549394-53549394 - PM-1 COSM5619976 c.10150A>C p.T3384P Substitution - Missense 23:53547829-53547829 - TCGA-AP-A05N-01 COSM1123178 c.6327A>G p.L2109L Substitution - coding silent 23:53569813-53569813 - TCGA-A6-6780-01 COSM1468574 c.11396C>T p.A3799V Substitution - Missense 23:53538987-53538987 - TCGA-BG-A0M4-01 COSM1123097 c.11338C>T p.R3780C Substitution - Missense 23:53543882-53543882 - TCGA-FW-A3TU-06 COSM3562413 c.797G>A p.G266D Substitution - Missense 23:53631000-53631000 - SNU-175 COSM2968355 c.9951C>T p.S3317S Substitution - coding silent 23:53549043-53549043 - TCGA-CU-A3KJ-01 COSM1315596 c.3566C>G p.S1189* Substitution - Nonsense 23:53593539-53593539 - 587232 COSM1210177 c.7838T>G p.V2613G Substitution - Missense 23:53559431-53559431 - MO_1012 COSM5565832 c.11009G>A p.R3670H Substitution - Missense 23:53543881-53543881 - 2492702 COSM5715751 c.8490C>T p.S2830S Substitution - coding silent 23:53552372-53552372 - OSCC-GB_00020111 COSM3713964 c.6979G>A p.E2327K Substitution - Missense 23:53561873-53561873 - 526T COSM4382098 c.9671G>A p.R3224H Substitution - Missense 23:53549323-53549323 - 2492711 COSM5718833 c.3237C>T p.V1079V Substitution - coding silent 23:53595330-53595330 - 8067242 COSM3780515 c.12358G>A p.D4120N Substitution - Missense 23:53536447-53536447 - 40M COSM5585443 c.10043C>T p.S3348F Substitution - Missense 23:53547936-53547936 - T3306 COSM4691588 c.6968C>A p.A2323D Substitution - Missense 23:53564635-53564635 - T2940 COSM4691580 c.7672G>T p.G2558C Substitution - Missense 23:53560252-53560252 - TCGA-66-2773-01 COSM756889 c.2332G>A p.E778K Substitution - Missense 23:53607687-53607687 - TCGA-AU-6004-01 COSM1468608 c.2882C>T p.A961V Substitution - Missense 23:53595274-53595274 - 23 COSM5015751 c.452T>C p.L151P Substitution - Missense 23:53645363-53645363 - MedB-1 COSM5621020 c.9913G>A p.A3305T Substitution - Missense 23:53548066-53548066 - Pat_32_B COSM5878055 c.7317_7319delGGA p.E2440delE Deletion - In frame 23:53562130-53562132 - LUAD-S01409 COSM388236 c.10102G>T p.G3368C Substitution - Missense 23:53548207-53548207 - TCGA-D8-A1XQ-01 COSM3845055 c.7172G>C p.S2391T Substitution - Missense 23:53562863-53562863 - MT-439-T2 COSM5651633 c.12050A>G p.Y4017C Substitution - Missense 23:53536425-53536425 - TCGA-AP-A0LM-01 COSM1123230 c.2359G>T p.D787Y Substitution - Missense 23:53607660-53607660 - CLL094 COSM1293028 c.11199C>A p.L3733L Substitution - coding silent 23:53544612-53544612 - TCGA-F4-6459-01 COSM1468562 c.12639G>C p.M4213I Substitution - Missense 23:53535394-53535394 - TCGA-13-0885-01 COSM4947471 c.9336G>C p.L3112L Substitution - coding silent 23:53550950-53550950 - TCGA-BR-4184-01 COSM4110147 c.11402C>T p.A3801V Substitution - Missense 23:53542517-53542517 - QC2-32-T2 COSM4419895 c.2109A>G p.S703S Substitution - coding silent 23:53614686-53614686 - TCGA-BR-8484-01 COSM4110204 c.360A>G p.T120T Substitution - coding silent 23:53645455-53645455 - EGC8 COSM5064759 c.12735G>A p.Q4245Q Substitution - coding silent 23:53534612-53534612 - TCGA-AD-6895-01 COSM1468580 c.10921G>T p.G3641C Substitution - Missense 23:53544560-53544560 - TCGA-AP-A056-01 COSM1123106 c.10765C>T p.P3589S Substitution - Missense 23:53544716-53544716 - HX32T COSM3708674 c.3405G>T p.S1135S Substitution - coding silent 23:53592554-53592554 - HCT116 COSM1682639 c.6484C>T p.R2162W Substitution - Missense 23:53569656-53569656 - PD22360a COSM5796062 c.11053G>C p.E3685Q Substitution - Missense 23:53542536-53542536 - TCGA-BP-4352-01 COSM3364167 c.7546G>A p.E2516K Substitution - Missense 23:53559019-53559019 - PD4120a COSM161634 c.12652G>C p.D4218H Substitution - Missense 23:53534047-53534047 - TCGA-32-2495-01 COSM191507 c.10875C>T p.D3625D Substitution - coding silent 23:53544606-53544606 - TCGA-FI-A2F8-01 COSM1123149 c.7934C>A p.P2645H Substitution - Missense 23:53559042-53559042 - TCGA-12-0616 COSM2153568 c.9611G>A p.R3204H Substitution - Missense 23:53549383-53549383 - S00831 COSM5660705 c.1537A>T p.N513Y Substitution - Missense 23:53625211-53625211 - TCGA-D1-A103-01 COSM1123152 c.7014C>T p.N2338N Substitution - coding silent 23:53561838-53561838 - Pat_55_A COSM5878058 c.4761_4762GG>AA p.A1588T Substitution - Missense 23:53583905-53583906 - ESO-250 COSM1254534 c.6882_6885delTCAG p.S2294fs*43 Deletion - Frameshift 23:53562153-53562156 - S0045 COSM5885058 c.883G>T p.E295* Substitution - Nonsense 23:53629596-53629596 - YUZINO COSM1714999 c.7021G>A p.E2341K Substitution - Missense 23:53564582-53564582 - OSCC-GB_01380111 COSM5953761 c.4111G>A p.E1371K Substitution - Missense 23:53590484-53590484 - YUSMI COSM5412851 c.9137G>A p.G3046E Substitution - Missense 23:53550687-53550687 - TCGA-AC-A23H-01 COSM3845068 c.2013C>T p.P671P Substitution - coding silent 23:53615780-53615780 - ESCC-F120 COSM5047135 c.7694_7695delCA p.T2565fs*4 Deletion - Frameshift 23:53558709-53558710 - MSK-PCa1_organoid COSM5423581 c.961_962insA p.M321fs*4 Insertion - Frameshift 23:53629517-53629518 - PD8621a COSM5789315 c.5919C>A p.T1973T Substitution - coding silent 23:53575754-53575754 - EOPC-139_tumor_01 COSM5950312 c.10161C>T p.A3387A Substitution - coding silent 23:53547818-53547818 - 2012-1349:2012-1312-T COSM4604540 c.1792C>A p.R598S Substitution - Missense 23:53617135-53617135 - TCGA-A2-A3XY-01 COSM3845031 c.12671C>T p.A4224V Substitution - Missense 23:53534676-53534676 - TCGA-G4-6302-01 COSM3694646 c.9770G>T p.R3257M Substitution - Missense 23:53548209-53548209 - BCB307T COSM4950136 c.6121G>T p.A2041S Substitution - Missense 23:53568867-53568867 - CLN4 COSM5024735 c.3156G>T p.L1052F Substitution - Missense 23:53600125-53600125 - T3670 COSM4691593 c.2833-5G>A p.? Unknown 23:53595328-53595328 - TCGA-A6-5665-01 COSM1468571 c.11987T>C p.V3996A Substitution - Missense 23:53538346-53538346 - YUNUFF COSM1715006 c.2104C>G p.P702A Substitution - Missense 23:53614691-53614691 - CHC892T COSM4796681 c.10111G>A p.A3371T Substitution - Missense 23:53548198-53548198 - Pat_27_B COSM5878056 c.6906_6908delGGA p.E2303delE Deletion - In frame 23:53562130-53562132 - XHDG32 COSM4769391 c.5923G>T p.V1975F Substitution - Missense 23:53569806-53569806 - CSCC-31-T COSM4565407 c.2084_2085CC>TT p.P695L Substitution - Missense 23:53614710-53614711 - TCGA-HU-A4GU-01 COSM2968347 c.10242C>T p.S3414S Substitution - coding silent 23:53548067-53548067 - sysucc-1163T COSM2968524 c.4616G>A p.R1539H Substitution - Missense 23:53584320-53584320 - TCGA-D8-A27F-01 COSM1491088 c.8342G>A p.G2781E Substitution - Missense 23:53554785-53554785 - sysucc-1030T COSM5452360 c.10835A>G p.D3612G Substitution - Missense 23:53546516-53546516 - TCGA-B8-4621-01 COSM488473 c.8701C>A p.Q2901K Substitution - Missense 23:53552687-53552687 - CHC892T COSM4959884 c.12975C>T p.I4325I Substitution - coding silent 23:53534054-53534054 - HN_63080 COSM123679 c.12199G>A p.E4067K Substitution - Missense 23:53536149-53536149 - TCGA-C8-A27B-01 COSM1491095 c.2548T>G p.S850A Substitution - Missense 23:53604783-53604783 - 526T COSM4382099 c.9341G>A p.R3114H Substitution - Missense 23:53549323-53549323 - CHC1715T COSM4789409 c.3292G>T p.A1098S Substitution - Missense 23:53595275-53595275 - TCGA-BS-A0UF-01 COSM1123140 c.8183G>A p.R2728K Substitution - Missense 23:53552875-53552875 - TCGA-34-2600-01 COSM756905 c.7320G>T p.L2440L Substitution - coding silent 23:53560193-53560193 - CLL094 COSM1293029 c.10869C>A p.L3623L Substitution - coding silent 23:53544612-53544612 - TCGA-BF-A1PV-01 COSM3562389 c.4553G>A p.R1518Q Substitution - Missense 23:53585049-53585049 - TCGA-43-6143-01 COSM756915 c.8873A>G p.D2958G Substitution - Missense 23:53551083-53551083 - CCK81 COSM2968624 c.780_781delCA p.I261fs*8 Deletion - Frameshift 23:53631016-53631017 - sysucc-1116T COSM5483144 c.2840G>A p.S947N Substitution - Missense 23:53595316-53595316 - LUAD-5V8LT COSM403175 c.12329G>C p.R4110P Substitution - Missense 23:53534688-53534688 - TCGA-21-1078-01 COSM756911 c.8119C>G p.P2707A Substitution - Missense 23:53554642-53554642 - T3090 COSM4492199 c.3934C>T p.R1312C Substitution - Missense 23:53592436-53592436 - AB COSM5414949 c.1728C>A p.L576L Substitution - coding silent 23:53617391-53617391 - HCC19 COSM1625991 c.1310A>G p.D437G Substitution - Missense 23:53627812-53627812 - TCGA-FU-A3HZ-01 COSM4840577 c.74A>C p.K25T Substitution - Missense 23:53648282-53648282 - TCGA-BH-A2L8-01 COSM3845039 c.11378C>T p.T3793M Substitution - Missense 23:53543842-53543842 - DM851T COSM673990 c.8962C>A p.Q2988K Substitution - Missense 23:53551400-53551400 - sysucc-1397T COSM5475350 c.9208C>T p.R3070C Substitution - Missense 23:53551078-53551078 - PT47 COSM5930394 c.11303-7A>G p.? Unknown 23:53539087-53539087 - SNU-C2B COSM2968488 c.5594A>T p.D1865V Substitution - Missense 23:53575668-53575668 - TCGA-B5-A0JY-01 COSM1123216 c.3979G>T p.D1327Y Substitution - Missense 23:53591116-53591116 - 29T COSM3713966 c.6794-1G>C p.? Unknown 23:53562245-53562245 - TCGA-D1-A16Y-01 COSM1123171 c.6223A>G p.I2075V Substitution - Missense 23:53568765-53568765 - TCGA-AN-A046-01 COSM3845037 c.11650G>A p.E3884K Substitution - Missense 23:53539063-53539063 - RK229_C01 COSM4780362 c.6218A>G p.N2073S Substitution - Missense 23:53568770-53568770 - S02347 COSM5694400 c.2164G>T p.A722S Substitution - Missense 23:53614631-53614631 - S0087 COSM5885056 c.10238T>G p.V3413G Substitution - Missense 23:53548071-53548071 - TCGA-60-2720-01 COSM756894 c.4383G>T p.V1461V Substitution - coding silent 23:53589625-53589625 - TCGA-61-1907-01 COSM1331798 c.12317A>T p.Y4106F Substitution - Missense 23:53536488-53536488 - 2492722 COSM5723310 c.8111C>T p.S2704F Substitution - Missense 23:53554650-53554650 - TCGA-G9-7510-01 COSM1472220 c.3595A>G p.M1199V Substitution - Missense 23:53591089-53591089 - 587338 COSM1210164 c.12379C>T p.R4127C Substitution - Missense 23:53534638-53534638 - TCGA-BG-A0M4-01 COSM1123098 c.11008C>T p.R3670C Substitution - Missense 23:53543882-53543882 - PTC-77C COSM4156908 c.6091G>A p.G2031R Substitution - Missense 23:53575161-53575161 - MDA-N COSM1682635 c.10220C>T p.S3407F Substitution - Missense 23:53548089-53548089 - MDA-N COSM1682636 c.9890C>T p.S3297F Substitution - Missense 23:53548089-53548089 - 2011-2289:2012-1332-T COSM4604424 c.1591+1G>T p.? Unknown 23:53625156-53625156 - QC2-22-T2 COSM5653120 c.11936A>G p.D3979G Substitution - Missense 23:53538397-53538397 - QC2-35-T2 COSM5655175 c.2409T>C p.V803V Substitution - coding silent 23:53607610-53607610 - TCGA-BS-A0UV-01 COSM1123185 c.5300G>A p.G1767E Substitution - Missense 23:53580836-53580836 - Pat_41_B COSM5878050 c.11203C>T p.P3735S Substitution - Missense 23:53539756-53539756 - TCGA-AP-A0LM-01 COSM1123259 c.4A>C p.K2Q Substitution - Missense 23:53654104-53654104 - CHC1061T COSM5349505 c.8232C>G p.Y2744* Substitution - Nonsense 23:53554895-53554895 - CLL135 COSM1293032 c.3740A>C p.K1247T Substitution - Missense 23:53593365-53593365 - TCGA-A2-A0ER-01 COSM457746 c.11357G>A p.R3786Q Substitution - Missense 23:53543863-53543863 - TCGA-BS-A0UF-01 COSM1123154 c.6983T>C p.M2328T Substitution - Missense 23:53561869-53561869 - HDC101 COSM4636204 c.6559G>A p.E2187K Substitution - Missense 23:53564633-53564633 - sysucc-1397T COSM5475351 c.8878C>T p.R2960C Substitution - Missense 23:53551078-53551078 - TCGA-FW-A3R5-06 COSM3914074 c.4757C>T p.P1586L Substitution - Missense 23:53583910-53583910 - TCGA-QU-A6IM-01 COSM4393188 c.9149C>T p.A3050V Substitution - Missense 23:53551137-53551137 - PD24202a COSM5774300 c.11081G>A p.R3694Q Substitution - Missense 23:53542508-53542508 - TCGA-EB-A431-01 COSM3562362 c.10575C>T p.T3525T Substitution - coding silent 23:53547734-53547734 - ESCC_BICR_017T COSM5442993 c.3601_3602insG p.A1201fs*17 Insertion - Frameshift 23:53593503-53593504 - T3021 COSM4691569 c.9800G>A p.R3267H Substitution - Missense 23:53549194-53549194 - Hx218 COSM50798 c.1261G>T p.D421Y Substitution - Missense 23:53627861-53627861 - PTC-28C COSM4156905 c.9432G>T p.K3144N Substitution - Missense 23:53549232-53549232 - CSCC-15-T COSM4506916 c.7336C>T p.Q2446* Substitution - Nonsense 23:53562113-53562113 - BB61T COSM50796 c.10990G>T p.A3664S Substitution - Missense 23:53543900-53543900 - TCGA-60-2710-01 COSM756900 c.6429G>T p.G2143G Substitution - coding silent 23:53569711-53569711 - TCGA-BS-A0UF-01 COSM1123192 c.5467C>T p.L1823F Substitution - Missense 23:53583611-53583611 - TCGA-A6-5665-01 COSM1123215 c.3879G>A p.P1293P Substitution - coding silent 23:53589718-53589718 - TCGA-BR-8487-01 COSM4110194 c.1554C>T p.A518A Substitution - coding silent 23:53625194-53625194 - TCGA-A7-A3J1-01 COSM3845059 c.6008C>T p.T2003M Substitution - Missense 23:53575665-53575665 - 8051974 COSM3390714 c.9082C>T p.R3028C Substitution - Missense 23:53550742-53550742 - TCGA-EB-A3XD-01 COSM3562351 c.11784C>T p.S3928S Substitution - coding silent 23:53537579-53537579 - TCGA-AP-A056-01 COSM1123065 c.12777C>T p.I4259I Substitution - coding silent 23:53534570-53534570 - T2458 COSM4691585 c.6830A>G p.E2277G Substitution - Missense 23:53562208-53562208 - TCGA-AX-A0J0-01 COSM1123100 c.10896G>T p.K3632N Substitution - Missense 23:53544585-53544585 - TCGA-B5-A0JY-01 COSM1123210 c.4496C>A p.A1499D Substitution - Missense 23:53588500-53588500 - TTC466 COSM4589484 c.8615G>T p.G2872V Substitution - Missense 23:53552773-53552773 - CHC1745T COSM4805847 c.11032G>T p.G3678C Substitution - Missense 23:53545045-53545045 - LUAD-GU4I3 COSM367849 c.9212G>A p.R3071H Substitution - Missense 23:53551074-53551074 - TCGA-AN-A046-01 COSM3845043 c.10582G>A p.V3528I Substitution - Missense 23:53547727-53547727 - T276 COSM4691596 c.1673-1_1673insT p.A558fs*3 Unknown 23:53617446-53617447 - SW948 COSM2968413 c.7219G>A p.G2407R Substitution - Missense 23:53560294-53560294 - 2011-2297:2012-323-T COSM4605644 c.5824A>G p.I1942V Substitution - Missense 23:53576960-53576960 - Gp5D COSM2968616 c.1259G>A p.G420D Substitution - Missense 23:53627863-53627863 - 2492722 COSM5723309 c.8477C>T p.S2826F Substitution - Missense 23:53554650-53554650 - HCC2998 COSM1682629 c.11180T>G p.L3727R Substitution - Missense 23:53544631-53544631 - TCGA-AX-A0J0-01 COSM1123156 c.6669C>T p.G2223G Substitution - coding silent 23:53563771-53563771 - T3225 COSM4691574 c.9238A>G p.S3080G Substitution - Missense 23:53551048-53551048 - TCGA-BR-6852-01 COSM4110155 c.10274G>A p.S3425N Substitution - Missense 23:53548035-53548035 - YUZINO COSM1715001 c.4069C>T p.P1357S Substitution - Missense 23:53591026-53591026 - TCGA-BS-A0UF-01 COSM1123153 c.7394T>C p.M2465T Substitution - Missense 23:53561869-53561869 - TCGA-RP-A695-06 COSM4896891 c.5005A>G p.N1669D Substitution - Missense 23:53584342-53584342 - TCGA-C5-A1MK-01 COSM4826820 c.8822G>A p.R2941Q Substitution - Missense 23:53552370-53552370 - PD6637a COSM3719912 c.6649G>T p.E2217* Substitution - Nonsense 23:53563791-53563791 - CSCC-41-T COSM4555324 c.6091G>A p.E2031K Substitution - Missense 23:53569638-53569638 - Pat_41_B COSM5878047 c.12818C>T p.S4273F Substitution - Missense 23:53534529-53534529 - TCGA-DA-A1HW-06 COSM3562410 c.1434G>A p.K478K Substitution - coding silent 23:53627465-53627465 - T256 COSM4691567 c.9834G>A p.K3278K Substitution - coding silent 23:53549160-53549160 - TCGA-D3-A2J8-06 COSM3562415 c.344C>T p.S115F Substitution - Missense 23:53647375-53647375 - LAU63 COSM232515 c.7733G>A p.R2578K Substitution - Missense 23:53558671-53558671 - TCGA-A2-A1FW-01 COSM1491096 c.1583T>C p.I528T Substitution - Missense 23:53625165-53625165 - TCGA-A6-5665-01 COSM1468584 c.10485A>G p.L3495L Substitution - coding silent 23:53546536-53546536 - TCGA-BK-A0C9-01 COSM1123164 c.6367C>T p.P2123S Substitution - Missense 23:53565169-53565169 - TCGA-BI-A0VR-01 COSM462205 c.12612C>T p.L4204L Substitution - coding silent 23:53534087-53534087 - CSCC-38-T COSM4461716 c.12184C>T p.L4062L Substitution - coding silent 23:53536621-53536621 - TCGA-61-2097-01 COSM71122 c.8368G>A p.V2790M Substitution - Missense 23:53552690-53552690 - TCGA-AA-3854-01 COSM271932 c.11180A>T p.K3727M Substitution - Missense 23:53539779-53539779 - Gp2D COSM2968617 c.1259G>A p.G420D Substitution - Missense 23:53627863-53627863 - CML036T COSM5803059 c.13070G>A p.R4357H Substitution - Missense 23:53533364-53533364 - 631056 COSM320897 c.11960C>G p.S3987C Substitution - Missense 23:53536515-53536515 - HCC2998 COSM1682629 c.11180T>G p.L3727R Substitution - Missense 23:53544631-53544631 - DM851T COSM673991 c.808C>A p.H270N Substitution - Missense 23:53630989-53630989 - ESCC_BICR_060T COSM5435211 c.11894A>G p.N3965S Substitution - Missense 23:53536581-53536581 - TCGA-EE-A2GO-06 COSM3562412 c.1414C>T p.P472S Substitution - Missense 23:53627485-53627485 - TCGA-AD-6964-01 COSM422535 c.5865A>G p.A1955A Substitution - coding silent 23:53576919-53576919 - TCGA-A6-6141-01 COSM305980 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - K154 COSM249439 c.7202G>T p.R2401L Substitution - Missense 23:53560311-53560311 - QC2-35-T2 COSM5655176 c.2409T>C p.V803V Substitution - coding silent 23:53607610-53607610 - TCGA-FU-A3HZ-01 COSM4840578 c.74A>C p.K25T Substitution - Missense 23:53648282-53648282 - HT115 COSM1123066 c.12447C>T p.I4149I Substitution - coding silent 23:53534570-53534570 - TCGA-AP-A051-01 COSM1123120 c.9918C>T p.G3306G Substitution - coding silent 23:53548061-53548061 - ACINAR06 COSM1734863 c.4014T>A p.D1338E Substitution - Missense 23:53589583-53589583 - TCGA-C5-A7CO-01 COSM4110143 c.12134G>A p.R4045Q Substitution - Missense 23:53537559-53537559 - ESCC_31 COSM4110140 c.12448G>C p.D4150H Substitution - Missense 23:53536230-53536230 - LIM1215 COSM4379676 c.2650A>G p.T884A Substitution - Missense 23:53604681-53604681 - LUAD-S01405 COSM404566 c.2284A>G p.I762V Substitution - Missense 23:53608887-53608887 - PD4112a COSM4810015 c.8459C>A p.T2820K Substitution - Missense 23:53554668-53554668 - 2011-2337:2012-307-T COSM4604243 c.13015C>G p.H4339D Substitution - Missense 23:53534014-53534014 - TCGA-66-2767-01 COSM756885 c.1990G>A p.D664N Substitution - Missense 23:53615803-53615803 - I2L-P5-Tumor-Organoid COSM5367340 c.5576G>A p.R1859H Substitution - Missense 23:53575686-53575686 - 587350 COSM1210166 c.7150C>T p.R2384C Substitution - Missense 23:53560363-53560363 - TCGA-B5-A11Y-01 COSM1123075 c.12173C>T p.A4058V Substitution - Missense 23:53536632-53536632 - PCSI_0090_Pa_X COSM3379656 c.4204-2A>G p.? Unknown 23:53586911-53586911 - TCGA-B5-A0JY-01 COSM1123206 c.4610T>G p.F1537C Substitution - Missense 23:53588386-53588386 - B59-Tumor COSM1757281 c.3949G>A p.V1317I Substitution - Missense 23:53592421-53592421 - CSCC-18-T COSM4572875 c.8586T>A p.F2862L Substitution - Missense 23:53551446-53551446 - 8058339 COSM3390711 c.12639G>A p.M4213I Substitution - Missense 23:53535394-53535394 - TCGA-B5-A11E-01 COSM1123181 c.5718G>T p.K1906N Substitution - Missense 23:53573933-53573933 - 169 COSM3729786 c.11175G>T p.R3725S Substitution - Missense 23:53544636-53544636 - B16 COSM1745399 c.3211_3219delGTTAAACTT p.V1071_L1073delVKL Deletion - In frame 23:53595348-53595356 - TCGA-43-6770-01 COSM756903 c.6366G>C p.Q2122H Substitution - Missense 23:53565170-53565170 - TCGA-CZ-4862-01 COSM1468591 c.9335T>A p.L3112Q Substitution - Missense 23:53550951-53550951 - CSCC-10-T COSM4488934 c.3401C>T p.S1134L Substitution - Missense 23:53594601-53594601 - 5_FL COSM4171955 c.4599A>T p.L1533F Substitution - Missense 23:53588397-53588397 - TCGA-D1-A16D-01 COSM1123221 c.3230C>T p.T1077M Substitution - Missense 23:53593464-53593464 - HCC2998 COSM1682625 c.11356C>T p.R3786W Substitution - Missense 23:53543864-53543864 - TCGA-BH-A18G-01 COSM3845064 c.3874G>A p.D1292N Substitution - Missense 23:53589723-53589723 - TCGA-GL-A59T-01 COSM3992540 c.8166T>C p.T2722T Substitution - coding silent 23:53557422-53557422 - AB COSM5414946 c.10095G>T p.R3365R Substitution - coding silent 23:53548214-53548214 - CHC1211T COSM4955000 c.9656G>T p.R3219L Substitution - Missense 23:53549338-53549338 - CML036T COSM5803060 c.12842G>A p.R4281H Substitution - Missense 23:53533364-53533364 - Pat_55_A COSM5878064 c.1517C>G p.A506G Substitution - Missense 23:53625231-53625231 - TCGA-C5-A7CO-01 COSM4110144 c.11804G>A p.R3935Q Substitution - Missense 23:53537559-53537559 - TCGA-B5-A0JZ-01 COSM1123093 c.11439C>A p.D3813E Substitution - Missense 23:53542480-53542480 - LS174T COSM2968546 c.3455A>G p.E1152G Substitution - Missense 23:53592504-53592504 - TCGA-FW-A3TU-06 COSM3562414 c.797G>A p.G266D Substitution - Missense 23:53631000-53631000 - ESCC_4 COSM5649968 c.12852_12854delACT p.L4286delL Deletion - In frame 23:53533352-53533354 - B96-Tumor COSM1757279 c.8131G>A p.D2711N Substitution - Missense 23:53558684-53558684 - CHC892T COSM4796682 c.9781G>A p.A3261T Substitution - Missense 23:53548198-53548198 - Gp5D COSM2968242 c.12940delC p.L4314fs*4 Deletion - Frameshift 23:53534089-53534089 - CSCC-10-T COSM4515490 c.11085_11086GG>AA p.E3696K Substitution - Missense 23:53542503-53542504 - ESCC-F10 COSM5046682 c.11317G>C p.D3773H Substitution - Missense 23:53543903-53543903 - S02290 COSM5686880 c.2441A>T p.D814V Substitution - Missense 23:53607578-53607578 - I2L-P19Ta-Tumor-Organoid COSM5367056 c.2014A>C p.T672P Substitution - Missense 23:53615779-53615779 - CHC429T COSM250785 c.1813C>G p.P605A Substitution - Missense 23:53617114-53617114 - TCGA-BR-4292-01 COSM4110171 c.7308G>A p.E2436E Substitution - coding silent 23:53562141-53562141 - TCGA-34-2600-01 COSM756904 c.7731G>T p.L2577L Substitution - coding silent 23:53560193-53560193 - LUAD-YINHD COSM388587 c.7698G>T p.K2566N Substitution - Missense 23:53558706-53558706 - TCGA-BF-A1PV-01 COSM3562388 c.4964G>A p.R1655Q Substitution - Missense 23:53585049-53585049 - YULLON COSM1714994 c.12488_12489CC>TT p.S4163F Substitution - Missense 23:53534528-53534529 - TCGA-D1-A16B-01 COSM1123116 c.10079C>T p.S3360L Substitution - Missense 23:53547900-53547900 - 2492729 COSM5726787 c.9275C>T p.T3092I Substitution - Missense 23:53549389-53549389 - OSCC-GB_00920111 COSM4881792 c.11582G>T p.R3861L Substitution - Missense 23:53538421-53538421 - CSCC-44-T COSM4451378 c.11575A>G p.I3859V Substitution - Missense 23:53538428-53538428 - CHC892T COSM4959884 c.12975C>T p.I4325I Substitution - coding silent 23:53534054-53534054 - KPOPBR-13-T COSM5963520 c.11554A>T p.S3852C Substitution - Missense 23:53539735-53539735 - T3306 COSM4691589 c.6557C>A p.A2186D Substitution - Missense 23:53564635-53564635 - 575 COSM3722116 c.12256A>G p.I4086V Substitution - Missense 23:53535447-53535447 - YUAKER COSM1715003 c.3815C>T p.S1272L Substitution - Missense 23:53592555-53592555 - S0087 COSM5885057 c.9908T>G p.V3303G Substitution - Missense 23:53548071-53548071 - TCGA-GM-A2D9-01 COSM3845053 c.7249C>G p.Q2417E Substitution - Missense 23:53562200-53562200 - TCGA-FS-A4FB-06 COSM3562373 c.9152A>G p.H3051R Substitution - Missense 23:53550672-53550672 - TCGA-AA-3492-01 COSM1468619 c.393G>A p.V131V Substitution - coding silent 23:53645422-53645422 - TCGA-B5-A11J-01 COSM1123102 c.10880C>T p.T3627M Substitution - Missense 23:53544601-53544601 - Pat_55_A COSM5878063 c.1517C>G p.A506G Substitution - Missense 23:53625231-53625231 - 2011-2267:2012-369-T COSM3992538 c.12005G>A p.R4002H Substitution - Missense 23:53537688-53537688 - 575 COSM3722115 c.12586A>G p.I4196V Substitution - Missense 23:53535447-53535447 - CSCC-27-T COSM4513272 c.8991C>T p.L2997L Substitution - coding silent 23:53550965-53550965 - Pat_40_A COSM5878062 c.3391C>T p.R1131* Substitution - Nonsense 23:53592568-53592568 - LC_C21 COSM1190561 c.10546G>A p.G3516R Substitution - Missense 23:53546475-53546475 - TCGA-AX-A060-01 COSM367849 c.9212G>A p.R3071H Substitution - Missense 23:53551074-53551074 - B59 COSM1757281 c.3949G>A p.V1317I Substitution - Missense 23:53592421-53592421 - TCGA-QU-A6IM-01 COSM4393189 c.8819C>T p.A2940V Substitution - Missense 23:53551137-53551137 - MO_1012 COSM5565831 c.11339G>A p.R3780H Substitution - Missense 23:53543881-53543881 - TCGA-AP-A051-01 COSM1123084 c.11612C>A p.P3871H Substitution - Missense 23:53538391-53538391 - CSCC-10-T COSM4488935 c.2990C>T p.S997L Substitution - Missense 23:53594601-53594601 - HCC122T COSM5808594 c.3504-2A>G p.? Unknown 23:53593603-53593603 - TCGA-AD-6964-01 COSM422536 c.5454A>G p.A1818A Substitution - coding silent 23:53576919-53576919 - Gp5D COSM2968565 c.3294G>A p.A1098A Substitution - coding silent 23:53595273-53595273 - 3844_T COSM3965374 c.6165C>T p.G2055G Substitution - coding silent 23:53573897-53573897 - TCGA-LL-A5YP-01 COSM4391492 c.4884G>T p.M1628I Substitution - Missense 23:53583783-53583783 - TCGA-AD-6895-01 COSM1468579 c.11251G>T p.G3751C Substitution - Missense 23:53544560-53544560 - TCGA-BS-A0UF-01 COSM1123068 c.12258C>A p.I4086I Substitution - coding silent 23:53535445-53535445 - XHDG39 COSM4770036 c.7223G>A p.R2408H Substitution - Missense 23:53560290-53560290 - BCM759T COSM5348805 c.1952_1953insATCC p.L652fs*15 Insertion - Frameshift 23:53616974-53616975 - MS4 COSM169409 c.11558G>A p.R3853H Substitution - Missense 23:53538445-53538445 - TCGA-BH-A0B0-01 COSM457751 c.6788G>A p.R2263Q Substitution - Missense 23:53562836-53562836 - TCGA-60-2710-01 COSM756901 c.6018G>T p.G2006G Substitution - coding silent 23:53569711-53569711 - Gp5D COSM2968549 c.3697T>A p.F1233I Substitution - Missense 23:53593408-53593408 - OSCC-GB_00020111 COSM3713963 c.7390G>A p.E2464K Substitution - Missense 23:53561873-53561873 - ESCC_31 COSM4110141 c.12118G>C p.D4040H Substitution - Missense 23:53536230-53536230 - 2011-2322:2012-352-T COSM4606110 c.9111G>T p.Q3037H Substitution - Missense 23:53551175-53551175 - 2011-2283:2012-316-T COSM4604684 c.2052A>G p.L684L Substitution - coding silent 23:53614743-53614743 - TCGA-BR-8484-01 COSM4110203 c.360A>G p.T120T Substitution - coding silent 23:53645455-53645455 - 2492720 COSM5723309 c.8477C>T p.S2826F Substitution - Missense 23:53554650-53554650 - S02384 COSM5698692 c.2787C>A p.H929Q Substitution - Missense 23:53600163-53600163 - TCGA-GL-A59T-01 COSM3992541 c.7800T>C p.T2600T Substitution - coding silent 23:53557422-53557422 - 2011-2267:2012-369-T COSM3992539 c.11675G>A p.R3892H Substitution - Missense 23:53537688-53537688 - TCGA-43-2578-01 COSM756924 c.10595C>A p.T3532N Substitution - Missense 23:53547714-53547714 - COLO201 COSM612993 c.2034G>T p.T678T Substitution - coding silent 23:53615759-53615759 - TCGA-A2-A0T5-01 COSM3845051 c.7618A>C p.T2540P Substitution - Missense 23:53560306-53560306 - T276 COSM4691597 c.1673-1_1673insT p.A558fs*3 Unknown 23:53617446-53617447 - TCGA-AZ-4315-01 COSM1468618 c.725C>T p.S242F Substitution - Missense 23:53631451-53631451 - TCGA-BS-A0UV-01 COSM1123091 c.11511G>T p.K3837N Substitution - Missense 23:53539778-53539778 - RK119_C01 COSM3766994 c.10583T>A p.I3528K Substitution - Missense 23:53546438-53546438 - CHC1715T COSM4789409 c.3292G>T p.A1098S Substitution - Missense 23:53595275-53595275 - TCGA-DD-A3A9-01 COSM4920858 c.12478C>G p.L4160V Substitution - Missense 23:53536200-53536200 - TCGA-B7-5816-01 COSM4110173 c.7140C>T p.D2380D Substitution - coding silent 23:53562895-53562895 - YUPROST COSM1715008 c.759G>C p.K253N Substitution - Missense 23:53631417-53631417 - OLID15 COSM132707 c.12203T>C p.V4068A Substitution - Missense 23:53535500-53535500 - TCGA-CJ-4900-01 COSM1497250 c.6625A>G p.M2209V Substitution - Missense 23:53568774-53568774 - HT115 COSM305980 c.183C>T p.F61F Substitution - coding silent 23:53647536-53647536 - TCGA-12-0616-01 COSM2153568 c.9611G>A p.R3204H Substitution - Missense 23:53549383-53549383 - TCGA-BR-8680-01 COSM4110182 c.4786A>G p.T1596A Substitution - Missense 23:53586528-53586528 - 2011-2260:2012-1319-T COSM4604233 c.12894G>T p.Q4298H Substitution - Missense 23:53534135-53534135 - PD4084a COSM4809997 c.5121C>A p.S1707R Substitution - Missense 23:53584226-53584226 - TCGA-AC-A23H-01 COSM3845062 c.4986G>C p.K1662N Substitution - Missense 23:53583681-53583681 - ESCC-F87 COSM5048971 c.11991C>G p.F3997L Substitution - Missense 23:53536484-53536484 - pfg108T COSM4755440 c.1586G>A p.R529Q Substitution - Missense 23:53625162-53625162 - TCGA-21-1070-01 COSM756918 c.10581C>T p.V3527V Substitution - coding silent 23:53547728-53547728 - 526T COSM4383218 c.11128A>G p.M3710V Substitution - Missense 23:53544683-53544683 - TCGA-D1-A103-01 COSM1123166 c.6636C>A p.I2212I Substitution - coding silent 23:53568763-53568763 - ESCC-240T COSM3940048 c.4976C>T p.T1659M Substitution - Missense 23:53585037-53585037 - TCGA-B3-8121-01 COSM3992543 c.6825G>A p.E2275E Substitution - coding silent 23:53562213-53562213 - S00837 COSM311890 c.9448_9449GG>CT p.G3150>? Complex 23:53549215-53549216 - TCGA-EE-A2GJ-06 COSM3562390 c.4429C>T p.R1477C Substitution - Missense 23:53589579-53589579 - Pat_66_A COSM5878060 c.3524G>A p.R1175H Substitution - Missense 23:53592435-53592435 - PM-2 COSM5619729 c.3794G>A p.R1265Q Substitution - Missense 23:53589803-53589803 - SNU-C2B COSM1123135 c.8840C>T p.P2947L Substitution - Missense 23:53552352-53552352 - S02384 COSM5698690 c.3364C>T p.R1122W Substitution - Missense 23:53592595-53592595 - RK181_C01 COSM3766998 c.7093G>A p.A2365T Substitution - Missense 23:53561759-53561759 - TCGA-EE-A3AF-06 COSM3562369 c.9463G>A p.E3155K Substitution - Missense 23:53549201-53549201 - TCGA-EE-A2GO-06 COSM3562358 c.11482G>T p.D3828Y Substitution - Missense 23:53539807-53539807 - TCGA-60-2710-01 COSM756927 c.10385T>A p.V3462E Substitution - Missense 23:53546747-53546747 - NYU939 COSM1210166 c.7150C>T p.R2384C Substitution - Missense 23:53560363-53560363 - TCGA-B5-A11Y-01 COSM1123215 c.3879G>A p.P1293P Substitution - coding silent 23:53589718-53589718 - T1154 COSM4691578 c.8268T>G p.S2756S Substitution - coding silent 23:53554859-53554859 - TCGA-BS-A0UV-01 COSM1123209 c.4179C>A p.I1393I Substitution - coding silent 23:53588406-53588406 - TCGA-06-0876 COSM2152060 c.10881C>T p.A3627A Substitution - coding silent 23:53546470-53546470 - 2011-2366:2012-1295-T COSM4605450 c.4293C>G p.L1431L Substitution - coding silent 23:53586820-53586820 - TCGA-D1-A17Q-01 COSM1123246 c.1397T>C p.L466S Substitution - Missense 23:53627502-53627502 - TCGA-AN-A046-01 COSM3845038 c.11320G>A p.E3774K Substitution - Missense 23:53539063-53539063 - TCGA-AP-A056-01 COSM1123195 c.4928G>A p.R1643H Substitution - Missense 23:53583739-53583739 - TCGA-CZ-5985-01 COSM488480 c.4189A>T p.T1397S Substitution - Missense 23:53588396-53588396 - CSCC-29-T COSM4569653 c.191T>C p.I64T Substitution - Missense 23:53647528-53647528 - TCGA-22-1016-01 COSM756930 c.12270C>T p.T4090T Substitution - coding silent 23:53536535-53536535 - TCGA-DK-A3IU-01 COSM3800674 c.8721G>C p.V2907V Substitution - coding silent 23:53551311-53551311 - TCGA-BR-8487-01 COSM4110153 c.10502C>T p.T3501M Substitution - Missense 23:53547807-53547807 - ESCC_101 COSM5637985 c.10612T>A p.Y3538N Substitution - Missense 23:53545135-53545135 - TCGA-DS-A1OC-01 COSM1294590 c.9118G>C p.G3040R Substitution - Missense 23:53550706-53550706 - CHC892T COSM4959885 c.12645C>T p.I4215I Substitution - coding silent 23:53534054-53534054 - TCGA-13-0887-01 COSM69357 c.8767-1G>T p.? Unknown 23:53551190-53551190 - TCGA-FI-A2F8-01 COSM1123150 c.7523C>A p.P2508H Substitution - Missense 23:53559042-53559042 - TCGA-A7-A26F-01 COSM3845065 c.4229C>A p.A1410D Substitution - Missense 23:53589779-53589779 - CSCC-15-T COSM4506917 c.6925C>T p.Q2309* Substitution - Nonsense 23:53562113-53562113 - T407 COSM4691586 c.7192G>A p.A2398T Substitution - Missense 23:53562843-53562843 - BRC11 COSM5028929 c.5744G>A p.R1915K Substitution - Missense 23:53577040-53577040 - TCGA-B6-A0I6-01 COSM457744 c.12240G>C p.L4080F Substitution - Missense 23:53536565-53536565 - TCGA-DU-7012-01 COSM3973738 c.1416G>A p.P472P Substitution - coding silent 23:53627483-53627483 - PD5925a COSM5788350 c.11653G>C p.D3885H Substitution - Missense 23:53538350-53538350 - 61 COSM3562364 c.10418A>G p.Q3473R Substitution - Missense 23:53547891-53547891 - 4095_T COSM3965373 c.6415G>C p.E2139Q Substitution - Missense 23:53565121-53565121 - TCGA-66-2800-01 COSM756883 c.637G>A p.E213K Substitution - Missense 23:53632495-53632495 - TCGA-BR-4368-01 COSM3406479 c.7081G>A p.G2361R Substitution - Missense 23:53563770-53563770 - NPC42F COSM4997147 c.6245A>G p.Y2082C Substitution - Missense 23:53573817-53573817 - TCGA-BR-4363-01 COSM4110177 c.5776A>G p.K1926E Substitution - Missense 23:53573875-53573875 - TCGA-CG-5721-01 COSM4110142 c.12245G>A p.R4082H Substitution - Missense 23:53536560-53536560 - TCGA-B5-A11E-01 COSM1123130 c.9202C>T p.R3068W Substitution - Missense 23:53549462-53549462 - ESCC_BICR_050T COSM488478 c.4457G>T p.R1486L Substitution - Missense 23:53585145-53585145 - TCGA-BK-A0C9-01 COSM1123163 c.6778C>T p.P2260S Substitution - Missense 23:53565169-53565169 - 587234 COSM1210175 c.7807C>T p.R2603W Substitution - Missense 23:53559462-53559462 - CX-1 COSM1682631 c.10895A>C p.Y3632S Substitution - Missense 23:53546456-53546456 - 3N50-VS-3T50 COSM4983207 c.6031-1G>A p.? Unknown 23:53575222-53575222 - S01563 COSM311891 c.6307G>A p.A2103T Substitution - Missense 23:53565229-53565229 - BN24T COSM1625987 c.2283T>C p.R761R Substitution - coding silent 23:53608888-53608888 - TCGA-EW-A1PC-01 COSM3845034 c.12142G>A p.V4048I Substitution - Missense 23:53536206-53536206 - TCGA-D1-A1NU-01 COSM1123224 c.3114C>T p.I1038I Substitution - coding silent 23:53600167-53600167 - T2940 COSM4691570 c.9574C>A p.L3192I Substitution - Missense 23:53549420-53549420 - TCGA-AP-A0LM-01 COSM1123260 c.4A>C p.K2Q Substitution - Missense 23:53654104-53654104 - 201 COSM3722117 c.5354T>C p.L1785P Substitution - Missense 23:53583724-53583724 - Patient_1 COSM5414244 c.12310C>T p.L4104F Substitution - Missense 23:53536495-53536495 - 2217529 COSM4421638 c.12117C>T p.P4039P Substitution - coding silent 23:53537576-53537576 - EOPC-139_tumor_01 COSM5950311 c.10491C>T p.A3497A Substitution - coding silent 23:53547818-53547818 - PD22357a COSM5784093 c.8336C>A p.T2779N Substitution - Missense 23:53552722-53552722 - CSCC-29-T COSM4569654 c.191T>C p.I64T Substitution - Missense 23:53647528-53647528 - TCGA-AA-3663-01 COSM1468606 c.3235C>A p.L1079I Substitution - Missense 23:53593459-53593459 - PD2205a COSM28420 c.12411A>T p.L4137F Substitution - Missense 23:53534606-53534606 - TCGA-AN-A0XW-01 COSM457759 c.529T>A p.F177I Substitution - Missense 23:53634274-53634274 - TCGA-B5-A11Y-01 COSM1123214 c.4290G>A p.P1430P Substitution - coding silent 23:53589718-53589718 - HT-29 COSM1682631 c.10895A>C p.Y3632S Substitution - Missense 23:53546456-53546456 - TCGA-AN-A046-01 COSM3845050 c.9028G>A p.A3010T Substitution - Missense 23:53550928-53550928 - TCGA-CD-A4MG-01 COSM4110157 c.10190A>G p.N3397S Substitution - Missense 23:53548119-53548119 - TCGA-RP-A695-06 COSM4896076 c.10709A>G p.K3570R Substitution - Missense 23:53546753-53546753 - PM-1 COSM5619975 c.10480A>C p.T3494P Substitution - Missense 23:53547829-53547829 - TCGA-AN-A0AK-01 COSM3845071 c.88A>G p.N30D Substitution - Missense 23:53648268-53648268 - TCGA-BR-4362-01 COSM2968645 c.329G>A p.R110Q Substitution - Missense 23:53647390-53647390 - TCGA-EE-A3JB-06 COSM4898779 c.1425C>T p.I475I Substitution - coding silent 23:53627474-53627474 - CHC892T COSM4796681 c.10111G>A p.A3371T Substitution - Missense 23:53548198-53548198 - 392 COSM3722113 c.2197G>A p.E733K Substitution - Missense 23:53614598-53614598 - S00837 COSM311890 c.9448_9449GG>CT p.G3150>? Complex 23:53549215-53549216 - TCGA-D1-A17Q-01 COSM1123245 c.1397T>C p.L466S Substitution - Missense 23:53627502-53627502 - TCGA-BS-A0UF-01 COSM1123123 c.9891G>T p.R3297S Substitution - Missense 23:53549103-53549103 - TCGA-B5-A11J-01 COSM1123101 c.11210C>T p.T3737M Substitution - Missense 23:53544601-53544601 - TCGA-A8-A06Z-01 COSM3845041 c.10851C>T p.D3617D Substitution - coding silent 23:53546500-53546500 - TCGA-A8-A09I-01 COSM457742 c.12603G>C p.E4201D Substitution - Missense 23:53535430-53535430 - 179T COSM1123162 c.6472G>A p.E2158K Substitution - Missense 23:53564720-53564720 - TCGA-AA-3492-01 COSM1468620 c.393G>A p.V131V Substitution - coding silent 23:53645422-53645422 - MDA-MB-435 COSM1682636 c.9890C>T p.S3297F Substitution - Missense 23:53548089-53548089 - TCGA-28-5218-01 COSM3406477 c.11080C>T p.R3694W Substitution - Missense 23:53542509-53542509 - 2T COSM3713963 c.7390G>A p.E2464K Substitution - Missense 23:53561873-53561873 - CSCC-10-T COSM4515489 c.11415_11416GG>AA p.E3806K Substitution - Missense 23:53542503-53542504 - 2011-2373:2012-1301-T COSM4604253 c.13096G>C p.E4366Q Substitution - Missense 23:53533338-53533338 - ESCC-240T COSM3940049 c.4565C>T p.T1522M Substitution - Missense 23:53585037-53585037 - HCT8 COSM4635813 c.9417G>T p.E3139D Substitution - Missense 23:53549247-53549247 - HCC2998 COSM2968607 c.1540T>C p.F514L Substitution - Missense 23:53625208-53625208 - TCGA-21-1070-01 COSM756923 c.10252G>T p.V3418L Substitution - Missense 23:53547727-53547727 - TCGA-CJ-4897-01 COSM488484 c.84T>G p.V28V Substitution - coding silent 23:53648272-53648272 - SNU-175 COSM2968356 c.9621C>T p.S3207S Substitution - coding silent 23:53549043-53549043 - 2T COSM3713964 c.6979G>A p.E2327K Substitution - Missense 23:53561873-53561873 - TCGA-AP-A056-01 COSM1123244 c.1557C>T p.I519I Substitution - coding silent 23:53625191-53625191 - TCGA-22-1016-01 COSM756931 c.11940C>T p.T3980T Substitution - coding silent 23:53536535-53536535 - CHC892T COSM4796436 c.6114G>A p.R2038R Substitution - coding silent 23:53568874-53568874 - TCGA-EE-A182-06 COSM3562353 c.11770C>T p.L3924L Substitution - coding silent 23:53537593-53537593 - PT26 COSM5905339 c.11638C>T p.R3880C Substitution - Missense 23:53538365-53538365 - HCC033T COSM5817922 c.11588C>T p.S3863F Substitution - Missense 23:53538415-53538415 - TCGA-D1-A16B-01 COSM1123115 c.10409C>T p.S3470L Substitution - Missense 23:53547900-53547900 - cSCCP7 COSM140326 c.8456G>C p.R2819T Substitution - Missense 23:53552406-53552406 - ESCC-164T COSM3940047 c.7198A>G p.T2400A Substitution - Missense 23:53560315-53560315 - T3090 COSM4492200 c.3523C>T p.R1175C Substitution - Missense 23:53592436-53592436 - S01542 COSM5669861 c.4819G>T p.E1607* Substitution - Nonsense 23:53583848-53583848 - sysucc-1510T COSM5764100 c.10961G>A p.R3654Q Substitution - Missense 23:53545116-53545116 - 2492714 COSM5718834 c.2833-7C>T p.? Unknown 23:53595330-53595330 - TCGA-AC-A5XS-01 COSM4390828 c.12980G>A p.R4327Q Substitution - Missense 23:53534049-53534049 - LUAD-S01346 COSM404347 c.12856C>T p.R4286C Substitution - Missense 23:53534173-53534173 - HCC2218 COSM23130 c.2838G>T p.R946S Substitution - Missense 23:53595318-53595318 - YUNUFF COSM1715005 c.2104C>G p.P702A Substitution - Missense 23:53614691-53614691 - 2492729 COSM5726786 c.9605C>T p.T3202I Substitution - Missense 23:53549389-53549389 - TCGA-EE-A3JI-06 COSM3562361 c.10570C>T p.L3524F Substitution - Missense 23:53546451-53546451 - LS180 COSM2968545 c.3866A>G p.E1289G Substitution - Missense 23:53592504-53592504 - TCGA-B5-A11G-01 COSM1123087 c.11768T>C p.L3923S Substitution - Missense 23:53538945-53538945 - TCGA-AX-A0J0-01 COSM1123155 c.7080C>T p.G2360G Substitution - coding silent 23:53563771-53563771 - TCGA-BS-A0UF-01 COSM1123177 c.6048G>T p.V2016V Substitution - coding silent 23:53569681-53569681 - BN24T COSM1625988 c.2283T>C p.R761R Substitution - coding silent 23:53608888-53608888 - TCGA-CG-5723-01 COSM4110163 c.7892A>G p.Q2631R Substitution - Missense 23:53559377-53559377 - TCGA-CC-A123-01 COSM4915309 c.7481A>G p.E2494G Substitution - Missense 23:53561782-53561782 - TCGA-A2-A0ER-01 COSM457747 c.11027G>A p.R3676Q Substitution - Missense 23:53543863-53543863 - BD124T COSM5494281 c.8159A>G p.Q2720R Substitution - Missense 23:53558656-53558656 - SJBALL021521_D1 COSM4994153 c.8407C>A p.P2803T Substitution - Missense 23:53554720-53554720 - YUPTER COSM5412859 c.3312C>T p.F1104F Substitution - coding silent 23:53593382-53593382 - ESCC_101 COSM5637984 c.10942T>A p.Y3648N Substitution - Missense 23:53545135-53545135 - PD8621a COSM5789316 c.5508C>A p.T1836T Substitution - coding silent 23:53575754-53575754 - 4095_T COSM3965372 c.6826G>C p.E2276Q Substitution - Missense 23:53565121-53565121 - PTC-77C COSM4156909 c.5680G>A p.G1894R Substitution - Missense 23:53575161-53575161 - AA COSM5414949 c.1728C>A p.L576L Substitution - coding silent 23:53617391-53617391 - S01542 COSM5669860 c.5230G>T p.E1744* Substitution - Nonsense 23:53583848-53583848 - YUROG COSM5412857 c.4249C>T p.L1417F Substitution - Missense 23:53586864-53586864 - ESO-114 COSM1254536 c.1824C>T p.F608F Substitution - coding silent 23:53617103-53617103 - LUAD_E00522 COSM388780 c.4864G>A p.D1622N Substitution - Missense 23:53585149-53585149 - ESCC-164T COSM3940046 c.7609A>G p.T2537A Substitution - Missense 23:53560315-53560315 - TCGA-A8-A06X-01 COSM457748 c.10756G>C p.E3586Q Substitution - Missense 23:53546706-53546706 - RK202_C01 COSM3766992 c.11032C>T p.Q3678* Substitution - Nonsense 23:53543858-53543858 - ESO-250 COSM1254533 c.7293_7296delTCAG p.S2431fs*43 Deletion - Frameshift 23:53562153-53562156 - TCGA-B5-A11N-01 COSM1123232 c.2354C>T p.T785I Substitution - Missense 23:53607665-53607665 - TCGA-D9-A3Z1-06 COSM3562407 c.1954C>T p.L652F Substitution - Missense 23:53616973-53616973 - RK197_C01 COSM3766996 c.10132T>A p.S3378T Substitution - Missense 23:53547847-53547847 - ESCC-D7 COSM5046452 c.94G>A p.E32K Substitution - Missense 23:53648262-53648262 - TCGA-B7-5816-01 COSM2968413 c.7219G>A p.G2407R Substitution - Missense 23:53560294-53560294 - HCT8 COSM4635815 c.7895C>T p.A2632V Substitution - Missense 23:53554866-53554866 - 18472 COSM5616343 c.5561A>G p.Y1854C Substitution - Missense 23:53575701-53575701 - TCGA-D1-A16Y-01 COSM1123170 c.6634A>G p.I2212V Substitution - Missense 23:53568765-53568765 - TCGA-EE-A29C-06 COSM3562401 c.2593C>T p.P865S Substitution - Missense 23:53604738-53604738 - YUPAER COSM5412854 c.6511G>A p.E2171K Substitution - Missense 23:53569629-53569629 - TCGA-D1-A101-01 COSM1123190 c.5504G>A p.R1835H Substitution - Missense 23:53583574-53583574 - TCGA-L6-A4EP-01 COSM3372295 c.1403G>A p.R468Q Substitution - Missense 23:53627496-53627496 - TCGA-AX-A0J0-01 COSM1123099 c.11226G>T p.K3742N Substitution - Missense 23:53544585-53544585 - LUAD-F00057 COSM365529 c.7105+1G>T p.? Unknown 23:53563745-53563745 - DN1401D COSM5961309 c.11258G>T p.C3753F Substitution - Missense 23:53539701-53539701 - TCGA-46-3769-01 COSM756877 c.515G>T p.G172V Substitution - Missense 23:53634288-53634288 - NCI-H23 COSM1196503 c.10291A>T p.T3431S Substitution - Missense 23:53547688-53547688 - PT52 COSM5941140 c.5906C>T p.P1969L Substitution - Missense 23:53575767-53575767 - TCGA-AM-5820-01 COSM2968622 c.792C>A p.A264A Substitution - coding silent 23:53631005-53631005 - TCGA-D3-A51T-06 COSM3562354 c.11718C>T p.S3906S Substitution - coding silent 23:53538995-53538995 - TCGA-D8-A1JA-01 COSM3845046 c.9800C>G p.S3267* Substitution - Nonsense 23:53548179-53548179 - P04-2666 COSM244975 c.3202C>T p.L1068L Substitution - coding silent 23:53593492-53593492 - TCGA-BR-8296-01 COSM2968365 c.9694C>T p.R3232C Substitution - Missense 23:53549300-53549300 - KYSE-180 COSM756913 c.8839G>T p.D2947Y Substitution - Missense 23:53551117-53551117 - RK202_C01 COSM3766991 c.11362C>T p.Q3788* Substitution - Nonsense 23:53543858-53543858 - App2312 COSM4169091 c.9092A>G p.E3031G Substitution - Missense 23:53551270-53551270 - BCB307T COSM4950135 c.6532G>T p.A2178S Substitution - Missense 23:53568867-53568867 - MT-439-T2 COSM5651632 c.12380A>G p.Y4127C Substitution - Missense 23:53536425-53536425 - B101 COSM1757278 c.9270C>T p.L3090L Substitution - coding silent 23:53549394-53549394 - TCGA-A8-A09I-01 COSM457743 c.12273G>C p.E4091D Substitution - Missense 23:53535430-53535430 - TCGA-BG-A0M4-01 COSM1123223 c.2789A>G p.Q930R Substitution - Missense 23:53600161-53600161 - TCGA-BH-A1FM-01 COSM1491091 c.7039C>T p.R2347C Substitution - Missense 23:53561813-53561813 - TCGA-B5-A0JY-01 COSM1123147 c.7972C>A p.L2658I Substitution - Missense 23:53559004-53559004 - TCGA-DD-A4NQ-01 COSM4941030 c.1105G>A p.A369T Substitution - Missense 23:53628761-53628761 - TCGA-EE-A29D-06 COSM3562376 c.8330C>T p.P2777L Substitution - Missense 23:53554797-53554797 - pfg151T COSM4755421 c.11708G>A p.R3903Q Substitution - Missense 23:53537655-53537655 - CSCC-56-T COSM4472037 c.1756C>A p.L586M Substitution - Missense 23:53617363-53617363 - TCGA-BS-A0UV-01 COSM1123121 c.10093C>T p.R3365W Substitution - Missense 23:53548216-53548216 - TCGA-09-2050-01 COSM78966 c.5297C>G p.S1766* Substitution - Nonsense 23:53580839-53580839 - PD4952a COSM5787960 c.11682G>A p.E3894E Substitution - coding silent 23:53537681-53537681 - TCGA-CU-A3KJ-01 COSM1315597 c.3155C>G p.S1052* Substitution - Nonsense 23:53593539-53593539 - S02255 COSM5681135 c.8614G>T p.G2872C Substitution - Missense 23:53552774-53552774 - SW403 COSM4655472 c.8547C>T p.S2849S Substitution - coding silent 23:53552841-53552841 - 587256 COSM1123098 c.11008C>T p.R3670C Substitution - Missense 23:53543882-53543882 - TCGA-EE-A2GM-06 COSM3562397 c.3063C>T p.L1021L Substitution - coding silent 23:53594528-53594528 - CSCC-27-T COSM4494128 c.3864C>T p.F1288F Substitution - coding silent 23:53589733-53589733 - TCGA-D1-A16X-01 COSM1123096 c.11052G>A p.S3684S Substitution - coding silent 23:53542537-53542537 - LC_S18 COSM1190563 c.5188A>G p.I1730V Substitution - Missense 23:53580948-53580948 - ESCC_BICR_017T COSM5442994 c.3190_3191insG p.A1064fs*17 Insertion - Frameshift 23:53593503-53593504 - OSCC-GB_00880111 COSM4888028 c.10882C>A p.R3628S Substitution - Missense 23:53544599-53544599 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.136905 Xp11.22 300697

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.1-24501T>G X 53705552 CLL A C Missense p.F4181C c.12542T>G X 53562452 BRCA A C Missense p.H3264Q c.9792T>G X 53576163 CM A C Missense p.S850A c.2548T>G X 53631744 BRCA A C Synonymous p.V28V c.84T>G X 53675215 RCCC A G Missense p.C49R c.145T>C X 53674517 LUSC A G Missense p.I528T c.1583T>C X 53652126 BRCA A G Missense p.L3923S c.11768T>C X 53565906 UCEC A G Missense p.S2026P c.6076T>C X 53602136 OV A G Synonymous p.D4261D c.12783T>C X 53561525 UCEC A G Synonymous p.P2296P c.6888T>C X 53591676 BRCA A G Synonymous p.T2070T c.6210T>C X 53600812 GBM - A IntronicInsertion . c.5717-62dupT X 53604089 ESCA A T IntronicSNV . c.2971+977T>A X 53628548 CLL A T Missense p.D1386E c.4158T>A X 53617397 BRCA A T Missense p.F177I c.529T>A X 53661226 BRCA A T Missense p.F3347Y c.10040T>A X 53575230 CM A T Missense p.L3112Q c.9335T>A X 53577912 RCCC A T Missense p.L3707Q c.11120T>A X 53571652 OV A T Missense p.L89Q c.266T>A X 53674396 LUAD A T Missense p.S1640T c.4918T>A X 53612055 OV A T Missense p.V3572E c.10715T>A X 53573708 LUSC A T Synonymous p.G2006G c.6018T>A X 53602615 BRCA C A IntronicSNV . c.8206+141G>T X 53584202 LGG C A Missense p.A2844S c.8530G>T X 53579819 NB C A Missense p.A3516S c.10546G>T X 53574724 LUAD C A Missense p.A4363S c.13087G>T X 53560308 HNSC C A Missense p.D3057Y c.9169G>T X 53578078 LUSC C A Missense p.E1701D c.5103G>T X 53611204 LUSC C A Missense p.E2412D c.7236G>T X 53589174 BRCA C A Missense p.G172V c.515G>T X 53661240 LUSC C A Missense p.G4011W c.12031G>T X 53564623 LUSC C A Missense p.G4156C c.12466G>T X 53563173 LUAD C A Missense p.G602V c.1805G>T X 53644083 LUAD C A Missense p.Q2343H c.7029G>T X 53591535 OV C A Missense p.R1083S c.3249G>T X 53622278 RCCC C A Missense p.R1623L c.4868G>T X 53612105 RCCC C A Missense p.R2690L c.8069G>T X 53585707 LUAD C A Missense p.S344I c.1031G>T X 53655786 STAD C A Missense p.V3528L c.10582G>T X 53574688 LUSC C A Missense p.V4178F c.12532G>T X 53562462 MM C A SpliceAcceptorSNV . c.9097-1G>T X 53578151 OV C A Synonymous p.G2143G c.6429G>T X 53596671 LUSC C A Synonymous p.L2577L c.7731G>T X 53587154 LUSC C A Synonymous p.R1259R c.3777G>T X 53619553 STAD C A Synonymous p.R3103R c.9309G>T X 53577938 HNSC C A Synonymous p.T678T c.2034G>T X 53642720 LUAD C A Synonymous p.V1461V c.4383G>T X 53616585 LUSC CC AG Missense p.G3260L c.9778_9779delinsCT X 53576176 SCLC CCA - InFrameDeletion p.G4060delG c.12177_12179delTGG X 53563587 HNSC C - Frameshift p.Q2333Sfs*19 c.6996delG X 53591568 GBM C G IntronicSNV . c.2049+33G>C X 53642672 NSCLC C G Missense p.D4328H c.12982G>C X 53561008 BRCA C G Missense p.E2819Q c.8455G>C X 53581633 BRCA C G Missense p.E3586Q c.10756G>C X 53573667 BRCA C G Missense p.E4201D c.12603G>C X 53562391 BRCA C G Missense p.E4354Q c.13060G>C X 53560335 BRCA C G Missense p.E87Q c.259G>C X 53674403 RCCC C G Missense p.G602A c.1805G>C X 53644083 BRCA C G Missense p.L3724F c.11172G>C X 53571600 COREAD C G Missense p.L4080F c.12240G>C X 53563526 BRCA C G Missense p.Q1997H c.5991G>C X 53602642 HNSC C G Missense p.Q2259H c.6777G>C X 53592131 LUSC C G Missense p.Q3037H c.9111G>C X 53578136 BLCA C G Missense p.Q499H c.1497G>C X 53652212 CM C G Missense p.R1377T c.4130G>C X 53617425 BLCA C G Missense p.R150P c.449G>C X 53672318 HNSC C G Missense p.R156S c.468G>C X 53672299 LUAD C G Synonymous p.L3112L c.9336G>C X 53577911 OV C G Synonymous p.V3017V c.9051G>C X 53578272 BLCA CTGA - Frameshift p.S2431Rfs*43 c.7293_7296delTCAG X 53589114 ESCA C T IntronicSNV . c.8881+32G>A X 53579240 NSCLC C T Missense p.A1201T c.3601G>A X 53620464 HNSC C T Missense p.A2240T c.6718G>A X 53592190 SCLC C T Missense p.D1031N c.3091G>A X 53627150 CM C T Missense p.D1303N c.3907G>A X 53619423 CM C T Missense p.D1986N c.5956G>A X 53602677 CM C T Missense p.D252N c.754G>A X 53658374 CM C T Missense p.D2611N c.7831G>A X 53586399 STAD C T Missense p.D2706N c.8116G>A X 53585660 UCEC C T Missense p.D348N c.1042G>A X 53655775 STAD C T Missense p.D3828N c.11482G>A X 53566768 BRCA C T Missense p.D4087N c.12259G>A X 53563507 HNSC C T Missense p.D56N c.166G>A X 53674496 HNSC C T Missense p.D650N c.1948G>A X 53643940 LUAD C T Missense p.D654N c.1960G>A X 53642794 CM C T Missense p.D664N c.1990G>A X 53642764 LUSC C T Missense p.E1350K c.4048G>A X 53618007 HNSC C T Missense p.E2047K c.6139G>A X 53600883 NB C T Missense p.E213K c.637G>A X 53659447 LUSC C T Missense p.E2419K c.7255G>A X 53589155 HNSC C T Missense p.E2653K c.7957G>A X 53585980 RCCC C T Missense p.E3265K c.9793G>A X 53576162 CM C T Missense p.E3771K c.11311G>A X 53570870 HNSC C T Missense p.E4149K c.12445G>A X 53563194 CM C T Missense p.E4149K c.12445G>A X 53563194 HNSC C T Missense p.E4177K c.12529G>A X 53563110 HNSC C T Missense p.E734K c.2200G>A X 53641556 CM C T Missense p.E778K c.2332G>A X 53634648 LUSC C T Missense p.G1060D c.3179G>A X 53622348 HNSC C T Missense p.G2361R c.7081G>A X 53590731 GBM C T Missense p.G2361R c.7081G>A X 53590731 STAD C T Missense p.G2781E c.8342G>A X 53581746 BRCA C T Missense p.G488E c.1463G>A X 53654387 HNSC C T Missense p.R1288Q c.3863G>A X 53619467 CM C T Missense p.R1655Q c.4964G>A X 53612009 CM C T Missense p.R1894H c.5681G>A X 53607826 LUAD C T Missense p.R1915K c.5744G>A X 53604000 BRCA C T Missense p.R2400Q c.7199G>A X 53589797 BRCA C T Missense p.R2400Q c.7199G>A X 53589797 HNSC C T Missense p.R2603Q c.7808G>A X 53586422 STAD C T Missense p.R3071H c.9212G>A X 53578035 UCEC C T Missense p.R3174H c.9521G>A X 53576434 COREAD C T Missense p.R3204H c.9611G>A X 53576344 GBM C T Missense p.R3739Q c.11216G>A X 53571556 HNSC C T Missense p.R3786Q c.11357G>A X 53570824 BRCA C T Missense p.R3963H c.11888G>A X 53565406 COREAD C T Missense p.R4045Q c.12134G>A X 53564520 STAD C T Missense p.R4063Q c.12188G>A X 53563578 SCLC C T Missense p.R4122H c.12365G>A X 53563401 HNSC C T Missense p.R4237H c.12710G>A X 53561598 BRCA C T Missense p.S2184N c.6551G>A X 53595808 OV C T Missense p.S3425N c.10274G>A X 53574996 STAD C T Missense p.V1510M c.4528G>A X 53615428 LUAD C T Missense p.V2900M c.8698G>A X 53579651 OV C T Missense p.V4207I c.12619G>A X 53562375 BRCA C T Synonymous p.E2436E c.7308G>A X 53589102 STAD C T Synonymous p.K478K c.1434G>A X 53654416 CM C T Synonymous p.L2553L c.7659G>A X 53587226 BLCA C T Synonymous p.P1430P c.4290G>A X 53616678 UCEC C T Synonymous p.Q3048Q c.9144G>A X 53578103 BLCA C T Synonymous p.R2694R c.8082G>A X 53585694 CM CTT - InFrameDeletion p.K4204delK c.12610_12612delAAG X 53562382 HNSC G A 5-UTRSNV . c.1-22C>T X 53681073 CM G A Missense p.A3050V c.9149C>T X 53578098 PRAD G A Missense p.A4058V c.12173C>T X 53563593 UCEC G A Missense p.L1554F c.4660C>T X 53613824 CM G A Missense p.L3457F c.10369C>T X 53574901 CM G A Missense p.L3634F c.10900C>T X 53573412 CM G A Missense p.L808F c.2422C>T X 53634558 HNSC G A Missense p.P1124L c.3371C>T X 53622156 CM G A Missense p.P1357S c.4069C>T X 53617986 HNSC G A Missense p.P1388S c.4162C>T X 53617393 CM G A Missense p.P3128S c.9382C>T X 53577865 CM G A Missense p.P3841L c.11522C>T X 53566728 CM G A Missense p.P3949L c.11846C>T X 53565828 CM G A Missense p.P472S c.1414C>T X 53654436 CM G A Missense p.P865S c.2593C>T X 53631699 CM G A Missense p.R1477C c.4429C>T X 53616539 CM G A Missense p.R2484C c.7450C>T X 53588774 BRCA G A Missense p.R3309C c.9925C>T X 53576030 LUAD G A Missense p.R3804W c.11410C>T X 53569470 GBM G A Missense p.R4334C c.13000C>T X 53560990 HNSC G A Missense p.S1139F c.3416C>T X 53621546 MM G A Missense p.S115F c.344C>T X 53674318 CM G A Missense p.S2034L c.6101C>T X 53600921 CM G A Missense p.S3407F c.10220C>T X 53575050 CM G A Missense p.S3461L c.10382C>T X 53574888 UCEC G A Missense p.S3470L c.10409C>T X 53574861 UCEC G A Missense p.S3929F c.11786C>T X 53565888 CM G A Missense p.S4030F c.12089C>T X 53564565 CM G A Missense p.S603F c.1808C>T X 53644080 CM G A Missense p.T1214M c.3641C>T X 53620424 UCEC G A Missense p.T2068I c.6203C>T X 53600819 CM G A Missense p.T3737M c.11210C>T X 53571562 UCEC G A Missense p.T43I c.128C>T X 53675171 LUAD G A Nonsense p.Q2259* c.6775C>T X 53592133 CLL G A Nonsense p.R1655* c.4963C>T X 53612010 GBM G A Synonymous p.A3627A c.10881C>T X 53573431 GBM G A Synonymous p.C49C c.147C>T X 53674515 STAD G A Synonymous p.D2380D c.7140C>T X 53589856 STAD G A Synonymous p.D2524D c.7572C>T X 53587313 STAD G A Synonymous p.D3735D c.11205C>T X 53571567 GBM G A Synonymous p.F1198F c.3594C>T X 53620471 CM G A Synonymous p.F2196F c.6588C>T X 53595771 BRCA G A Synonymous p.F608F c.1824C>T X 53644064 ESCA G A Synonymous p.G3319G c.9957C>T X 53575998 CM G A Synonymous p.G420G c.1260C>T X 53654813 STAD G A Synonymous p.G878G c.2634C>T X 53631658 HNSC G A Synonymous p.I1038I c.3114C>T X 53627127 UCEC G A Synonymous p.I2543I c.7629C>T X 53587256 COREAD G A Synonymous p.I475I c.1425C>T X 53654425 CM G A Synonymous p.L1158L c.3474C>T X 53621488 CM G A Synonymous p.L2592L c.7774C>T X 53586456 CM G A Synonymous p.L2985L c.8953C>T X 53578370 LUAD G A Synonymous p.L4034L c.12100C>T X 53564554 CM G A Synonymous p.S1311S c.3933C>T X 53619397 HNSC G A Synonymous p.T4090T c.12270C>T X 53563496 LUSC G A Synonymous p.V134V c.402C>T X 53672365 BLCA G A Synonymous p.V3527V c.10581C>T X 53574689 LUSC GCCGGGGCCGGGGCCGGGGCCGGT - IntronicDeletion . c.1490-633_1490-610delACCGGCCCCGGCCCCGGCCCCGGC X 53652829 STAD GCCGGT - IntronicDeletion . c.1490-633_1490-628delACCGGC X 53652847 STAD G C Missense p.A2165G c.6494C>G X 53596606 COREAD G C Missense p.H530D c.1588C>G X 53652121 THCA G C Missense p.I903M c.2709C>G X 53631583 BLCA G C Missense p.L1325V c.3973C>G X 53618082 LGG G C Missense p.L4104V c.12310C>G X 53563456 LUAD G C Missense p.P2829A c.8485C>G X 53581603 LUSC G C Missense p.Q1316E c.3946C>G X 53619384 HNSC G C Missense p.S2789C c.8366C>G X 53581722 LUAD G C Missense p.S4097C c.12290C>G X 53563476 SCLC G C Missense p.S726C c.2177C>G X 53641579 LUSC G C Missense p.T220R c.659C>G X 53658553 HNSC G C Nonsense p.S1189* c.3566C>G X 53620499 BLCA G C Nonsense p.S1600* c.4799C>G X 53613475 HNSC G C Nonsense p.S1903* c.5708C>G X 53607799 OV - G Frameshift p.S2508Ifs*81 c.7520dupC X 53587365 HNSC GT AA Missense p.H3273Y c.9816_9817delinsTT X 53576138 CM GTG - InFrameDeletion p.T3496delT c.10485_10487delCAC X 53574783 CM G T Missense p.A180E c.539C>A X 53661216 LGG G T Missense p.D3813E c.11439C>A X 53569441 UCEC G T Missense p.L3269M c.9805C>A X 53576150 CM G T Missense p.P1140T c.3418C>A X 53621544 CM G T Missense p.P1223T c.3667C>A X 53620398 CM G T Missense p.P2977H c.8930C>A X 53578393 LUAD G T Missense p.P3012T c.9034C>A X 53578289 RCCC G T Missense p.Q2901K c.8701C>A X 53579648 RCCC G T Missense p.Q2912K c.8734C>A X 53579615 CM G T Missense p.Q381K c.1141C>A X 53655545 OV G T Missense p.R3628S c.10882C>A X 53573430 CM G T Missense p.S1707R c.5121C>A X 53611186 BRCA G T Missense p.S3936Y c.11807C>A X 53565867 STAD G T Missense p.T2820K c.8459C>A X 53581629 BRCA G T Missense p.T3532N c.10595C>A X 53574675 LUSC G T Synonymous p.G1749G c.5247C>A X 53610791 LUSC G T Synonymous p.I2615I c.7845C>A X 53586385 RCCC G T Synonymous p.L3733L c.11199C>A X 53571573 CLL G T Synonymous p.T984T c.2952C>A X 53629544 LUAD T A Missense p.D664V c.1991A>T X 53642763 COREAD T A Missense p.K3837M c.11510A>T X 53566740 COREAD T A Missense p.Q791L c.2372A>T X 53634608 LUAD T A Missense p.S727C c.2179A>T X 53641577 LUAD T A Missense p.T1534S c.4600A>T X 53615356 RCCC T A SpliceAcceptorSNV . c.10759-2A>T X 53573555 HNSC T A Synonymous p.G172G c.516A>T X 53661239 LUSC T A Synonymous p.S1903S c.5709A>T X 53607798 LUAD T A Synonymous p.T2859T c.8577A>T X 53579772 RCCC T C Missense p.D3068G c.9203A>G X 53578044 LUSC T C Missense p.E1734G c.5201A>G X 53610837 COREAD T C Missense p.H3109R c.9326A>G X 53577921 OV T C Missense p.I2212V c.6634A>G X 53595725 UCEC T C Missense p.I226V c.676A>G X 53658536 ESCA T C Missense p.I3638V c.10912A>G X 53573400 HNSC T C Missense p.I920V c.2758A>G X 53630447 SCLC T C Missense p.K2063E c.6187A>G X 53600835 STAD T C Missense p.M1336V c.4006A>G X 53618049 PRAD T C Missense p.N1717S c.5150A>G X 53611157 STAD T C Missense p.N1890S c.5669A>G X 53607838 UCEC T C Missense p.N2244D c.6730A>G X 53592178 CM T C Missense p.T1837A c.5509A>G X 53610529 LUAD T C Missense p.T340A c.1018A>G X 53655799 ESCA T C Missense p.T3483A c.10447A>G X 53574823 LUSC T C Missense p.Y1991C c.5972A>G X 53602661 NSCLC T C Synonymous p.A1955A c.5865A>G X 53603879 BLCA T C Synonymous p.G152G c.456A>G X 53672311 BRCA T C Synonymous p.K509K c.1527A>G X 53652182 HC T C Synonymous p.L2109L c.6327A>G X 53596773 UCEC T C Synonymous p.P1040P c.3120A>G X 53627121 UCEC T C Synonymous p.Q3094Q c.9282A>G X 53577965 CM T G Missense p.D654A c.1961A>C X 53642793 CM T G Missense p.E2653D c.7959A>C X 53585978 HC T G Missense p.I3692L c.11074A>C X 53571698 HNSC T G Missense p.K1247T c.3740A>C X 53620325 CLL T G Missense p.K839N c.2517A>C X 53631775 STAD