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 15 51755647 51755647 + Missense_Mutation SNP G G A TCGA-OR-A5J8-01A-11D-A29I-10 TCGA-OR-A5J8-10A-01D-A29L-10 g.chr15:51755647G>A c.7852C>T c.(7852-7854)Ctt>Ttt p.L2618F ACC 15 51756879 51756879 + Missense_Mutation SNP G G T TCGA-OR-A5KS-01A-11D-A30A-10 TCGA-OR-A5KS-10A-01D-A30A-10 g.chr15:51756879G>T c.7798C>A c.(7798-7800)Cca>Aca p.P2600T BLCA 15 51741195 51741195 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:51741195G>T c.9097C>A c.(9097-9099)Ctt>Att p.L3033I BLCA 15 51741202 51741202 + Missense_Mutation SNP G G T TCGA-G2-A3IB-01A-11D-A20D-08 TCGA-G2-A3IB-10A-01D-A20D-08 g.chr15:51741202G>T c.9090C>A c.(9088-9090)aaC>aaA p.N3030K BLCA 15 51741241 51741241 + Silent SNP C C A TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr15:51741241C>A c.9051G>T c.(9049-9051)ctG>ctT p.L3017L BLCA 15 51741242 51741242 + Missense_Mutation SNP A A G TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr15:51741242A>G c.9050T>C c.(9049-9051)cTg>cCg p.L3017P BLCA 15 51742421 51742421 + Missense_Mutation SNP G G T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr15:51742421G>T c.8806C>A c.(8806-8808)Cac>Aac p.H2936N BLCA 15 51745781 51745781 + Missense_Mutation SNP G G C TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr15:51745781G>C c.8596C>G c.(8596-8598)Cta>Gta p.L2866V BLCA 15 51749535 51749535 + Missense_Mutation SNP C C G TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr15:51749535C>G c.8261G>C c.(8260-8262)gGa>gCa p.G2754A BLCA 15 51749644 51749644 + Missense_Mutation SNP G G A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr15:51749644G>A c.8152C>T c.(8152-8154)Cgt>Tgt p.R2718C BLCA 15 51750971 51750971 + Missense_Mutation SNP G G A TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr15:51750971G>A c.7945C>T c.(7945-7947)Cca>Tca p.P2649S BLCA 15 51755626 51755626 + Nonsense_Mutation SNP G G A TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr15:51755626G>A c.7873C>T c.(7873-7875)Caa>Taa p.Q2625* BLCA 15 51757070 51757070 + Missense_Mutation SNP A A G TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr15:51757070A>G c.7607T>C c.(7606-7608)cTg>cCg p.L2536P BLCA 15 51758397 51758397 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:51758397C>T c.7501G>A c.(7501-7503)Gat>Aat p.D2501N BLCA 15 51758463 51758463 + Missense_Mutation SNP C C T TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr15:51758463C>T c.7435G>A c.(7435-7437)Gaa>Aaa p.E2479K BLCA 15 51758502 51758502 + Missense_Mutation SNP G G C TCGA-BT-A20R-01A-12D-A16O-08 TCGA-BT-A20R-11A-11D-A16O-08 g.chr15:51758502G>C c.7396C>G c.(7396-7398)Ctt>Gtt p.L2466V BLCA 15 51768876 51768876 + Missense_Mutation SNP G G C TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr15:51768876G>C c.6871C>G c.(6871-6873)Caa>Gaa p.Q2291E BLCA 15 51772275 51772275 + Missense_Mutation SNP G G A TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr15:51772275G>A c.6626C>T c.(6625-6627)tCa>tTa p.S2209L BLCA 15 51772275 51772275 + Missense_Mutation SNP G G A TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr15:51772275G>A c.6626C>T c.(6625-6627)tCa>tTa p.S2209L BLCA 15 51772766 51772766 + Silent SNP G G C TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr15:51772766G>C c.6537C>G c.(6535-6537)ctC>ctG p.L2179L BLCA 15 51772832 51772832 + Silent SNP T T A TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr15:51772832T>A c.6471A>T c.(6469-6471)gtA>gtT p.V2157V BLCA 15 51772908 51772908 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:51772908C>G c.6395G>C c.(6394-6396)aGa>aCa p.R2132T BLCA 15 51772963 51772963 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:51772963C>T c.6340G>A c.(6340-6342)Gaa>Aaa p.E2114K BLCA 15 51772972 51772972 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:51772972C>G c.6331G>C c.(6331-6333)Gat>Cat p.D2111H BLCA 15 51772975 51772975 + Silent SNP G G A TCGA-XF-A9SZ-01A-11D-A391-08 TCGA-XF-A9SZ-10A-01D-A394-08 g.chr15:51772975G>A c.6328C>T c.(6328-6330)Ctg>Ttg p.L2110L BLCA 15 51772987 51772987 + Missense_Mutation SNP C C G TCGA-FD-A5BX-01A-11D-A26M-08 TCGA-FD-A5BX-10A-01D-A26K-08 g.chr15:51772987C>G c.6316G>C c.(6316-6318)Gag>Cag p.E2106Q BLCA 15 51773227 51773227 + Missense_Mutation SNP C C G TCGA-FD-A5C1-01A-11D-A289-08 TCGA-FD-A5C1-10A-01D-A289-08 g.chr15:51773227C>G c.6076G>C c.(6076-6078)Gag>Cag p.E2026Q BLCA 15 51773374 51773374 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:51773374C>G c.5929G>C c.(5929-5931)Gat>Cat p.D1977H BLCA 15 51773566 51773566 + Missense_Mutation SNP T T C TCGA-BT-A20N-01A-11D-A14W-08 TCGA-BT-A20N-11A-11D-A14W-08 g.chr15:51773566T>C c.5737A>G c.(5737-5739)Aaa>Gaa p.K1913E BLCA 15 51778370 51778370 + Frame_Shift_Del DEL A A - TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr15:51778370delA c.5382delT c.(5380-5382)gatfs p.D1794fs BLCA 15 51778495 51778495 + Missense_Mutation SNP C C T TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr15:51778495C>T c.5257G>A c.(5257-5259)Gtt>Att p.V1753I BLCA 15 51780153 51780153 + Missense_Mutation SNP C C G TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr15:51780153C>G c.5215G>C c.(5215-5217)Gag>Cag p.E1739Q BLCA 15 51780819 51780819 + Silent SNP C C T TCGA-E7-A97Q-01A-11D-A38G-08 TCGA-E7-A97Q-10A-01D-A38J-08 g.chr15:51780819C>T c.4977G>A c.(4975-4977)agG>agA p.R1659R BLCA 15 51783938 51783938 + Missense_Mutation SNP G G C TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr15:51783938G>C c.4790C>G c.(4789-4791)tCt>tGt p.S1597C BLCA 15 51790751 51790751 + Missense_Mutation SNP G G A TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr15:51790751G>A c.4670C>T c.(4669-4671)tCa>tTa p.S1557L BLCA 15 51791053 51791054 + Frame_Shift_Ins INS - - T TCGA-ZF-AA4T-01A-11D-A38G-08 TCGA-ZF-AA4T-10A-01D-A38J-08 g.chr15:51791053_51791054insT c.4367_4368insA c.(4366-4368)tatfs p.Y1456fs BLCA 15 51791498 51791498 + Missense_Mutation SNP C C G TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr15:51791498C>G c.3923G>C c.(3922-3924)aGa>aCa p.R1308T BLCA 15 51791720 51791720 + Missense_Mutation SNP C C G TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr15:51791720C>G c.3701G>C c.(3700-3702)aGa>aCa p.R1234T BLCA 15 51791720 51791720 + Missense_Mutation SNP C C T TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr15:51791720C>T c.3701G>A c.(3700-3702)aGa>aAa p.R1234K BLCA 15 51791785 51791785 + Silent SNP A A G TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr15:51791785A>G c.3636T>C c.(3634-3636)gcT>gcC p.A1212A BLCA 15 51792343 51792343 + Missense_Mutation SNP G G C TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr15:51792343G>C c.3078C>G c.(3076-3078)ttC>ttG p.F1026L BLCA 15 51795035 51795035 + Missense_Mutation SNP G G A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr15:51795035G>A c.2960C>T c.(2959-2961)tCa>tTa p.S987L BLCA 15 51827926 51827926 + Silent SNP C C G TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr15:51827926C>G c.2370G>C c.(2368-2370)ctG>ctC p.L790L BLCA 15 51829744 51829744 + Missense_Mutation SNP G G C TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr15:51829744G>C c.1558C>G c.(1558-1560)Cta>Gta p.L520V BLCA 15 51834543 51834543 + Silent SNP G G A TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr15:51834543G>A c.1092C>T c.(1090-1092)atC>atT p.I364I BLCA 15 51834638 51834638 + Missense_Mutation SNP C C G TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr15:51834638C>G c.997G>C c.(997-999)Gaa>Caa p.E333Q BLCA 15 51837962 51837962 + Splice_Site SNP C C A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr15:51837962C>A c.748G>T c.(748-750)Ggt>Tgt p.G250C BLCA 15 51857288 51857288 + Missense_Mutation SNP G G C TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr15:51857288G>C c.361C>G c.(361-363)Caa>Gaa p.Q121E BRCA 15 51742471 51742471 + Missense_Mutation SNP C C T TCGA-E2-A1IH-01A-11D-A188-09 TCGA-E2-A1IH-10A-01D-A13O-09 g.chr15:51742471C>T c.8756G>A c.(8755-8757)gGt>gAt p.G2919D BRCA 15 51756941 51756941 + Missense_Mutation SNP A A T TCGA-A7-A5ZV-01A-11D-A28B-09 TCGA-A7-A5ZV-10A-01D-A28E-09 g.chr15:51756941A>T c.7736T>A c.(7735-7737)cTt>cAt p.L2579H BRCA 15 51766573 51766575 + In_Frame_Del DEL ACA ACA - TCGA-AC-A2QH-01A-11D-A18P-09 TCGA-AC-A2QH-10A-01D-A18P-09 g.chr15:51766573_51766575delACA c.7176_7178delTGT c.(7174-7179)gttgtg>gtg p.2392_2393VV>V BRCA 15 51766785 51766785 + Silent SNP C C G TCGA-AR-A1AI-01A-11D-A12Q-09 TCGA-AR-A1AI-10A-01D-A12Q-09 g.chr15:51766785C>G c.6966G>C c.(6964-6966)gtG>gtC p.V2322V BRCA 15 51772888 51772888 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:51772888C>G c.6415G>C c.(6415-6417)Gag>Cag p.E2139Q BRCA 15 51773047 51773047 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:51773047C>T c.6256G>A c.(6256-6258)Gag>Aag p.E2086K BRCA 15 51773279 51773279 + Silent SNP T T C TCGA-EW-A1P4-01A-21D-A142-09 TCGA-EW-A1P4-10A-01D-A142-09 g.chr15:51773279T>C c.6024A>G c.(6022-6024)aaA>aaG p.K2008K BRCA 15 51773348 51773348 + Silent SNP G G A TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr15:51773348G>A c.5955C>T c.(5953-5955)gcC>gcT p.A1985A BRCA 15 51773769 51773769 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:51773769C>T c.5534G>A c.(5533-5535)cGa>cAa p.R1845Q BRCA 15 51778354 51778354 + Missense_Mutation SNP G G A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr15:51778354G>A c.5398C>T c.(5398-5400)Ctt>Ttt p.L1800F BRCA 15 51778522 51778522 + Missense_Mutation SNP T T G TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:51778522T>G c.5230A>C c.(5230-5232)Aaa>Caa p.K1744Q BRCA 15 51778534 51778534 + Splice_Site SNP C C A TCGA-A8-A094-01A-11W-A019-09 TCGA-A8-A094-10A-01W-A021-09 g.chr15:51778534C>A c.5218G>T c.(5218-5220)Gta>Tta p.V1740L BRCA 15 51780803 51780803 + Missense_Mutation SNP C C G TCGA-E9-A3QA-01A-61D-A228-09 TCGA-E9-A3QA-10A-01D-A22A-09 g.chr15:51780803C>G c.4993G>C c.(4993-4995)Gat>Cat p.D1665H BRCA 15 51780830 51780830 + Frame_Shift_Del DEL A A - TCGA-AQ-A54O-01A-11D-A25Q-09 TCGA-AQ-A54O-10A-01D-A25Q-09 g.chr15:51780830delA c.4966delT c.(4966-4968)tctfs p.S1656fs BRCA 15 51783884 51783884 + Missense_Mutation SNP T T C TCGA-A8-A097-01A-11W-A050-09 TCGA-A8-A097-10A-01D-A047-09 g.chr15:51783884T>C c.4844A>G c.(4843-4845)aAt>aGt p.N1615S BRCA 15 51787275 51787275 + Missense_Mutation SNP T T C TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr15:51787275T>C c.4729A>G c.(4729-4731)Aca>Gca p.T1577A BRCA 15 51790768 51790768 + Frame_Shift_Del DEL G G - TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr15:51790768delG c.4653delC c.(4651-4653)agcfs p.S1551fs BRCA 15 51790773 51790774 + Frame_Shift_Del DEL CA CA - TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr15:51790773_51790774delCA c.4647_4648delTG c.(4645-4650)gatgaafs p.D1549fs BRCA 15 51791403 51791403 + Missense_Mutation SNP G G T TCGA-E9-A1NC-01A-12W-A16L-09 TCGA-E9-A1NC-10A-01D-A159-09 g.chr15:51791403G>T c.4018C>A c.(4018-4020)Ctt>Att p.L1340I BRCA 15 51791547 51791547 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:51791547C>T c.3874G>A c.(3874-3876)Gag>Aag p.E1292K BRCA 15 51792037 51792037 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:51792037C>A c.3384G>T c.(3382-3384)ttG>ttT p.L1128F BRCA 15 51799419 51799419 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:51799419G>T c.2676C>A c.(2674-2676)ttC>ttA p.F892L BRCA 15 51828435 51828435 + Missense_Mutation SNP T T G TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr15:51828435T>G c.2242A>C c.(2242-2244)Att>Ctt p.I748L BRCA 15 51828902 51828902 + Nonsense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr15:51828902G>C c.1775C>G c.(1774-1776)tCa>tGa p.S592* BRCA 15 51828921 51828921 + Missense_Mutation SNP C C G TCGA-A2-A04T-01A-21W-A050-09 TCGA-A2-A04T-10A-01W-A055-09 g.chr15:51828921C>G c.1756G>C c.(1756-1758)Gta>Cta p.V586L BRCA 15 51837848 51837848 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr15:51837848T>G c.862A>C c.(862-864)Act>Cct p.T288P BRCA 15 51857358 51857358 + Silent SNP G G C TCGA-AC-A2B8-01A-11D-A17D-09 TCGA-AC-A2B8-10A-01D-A17D-09 g.chr15:51857358G>C c.291C>G c.(289-291)ctC>ctG p.L97L CESC 15 51748511 51748511 + Missense_Mutation SNP T T C TCGA-HG-A2PA-01A-11D-A20U-09 TCGA-HG-A2PA-10B-01D-A20U-09 g.chr15:51748511T>C c.8327A>G c.(8326-8328)cAa>cGa p.Q2776R CESC 15 51748512 51748512 + Missense_Mutation SNP G G C TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr15:51748512G>C c.8326C>G c.(8326-8328)Caa>Gaa p.Q2776E CESC 15 51755661 51755661 + Missense_Mutation SNP C C T TCGA-DS-A0VN-01A-21D-A10S-08 TCGA-DS-A0VN-10A-01D-A10S-08 g.chr15:51755661C>T c.7838G>A c.(7837-7839)cGa>cAa p.R2613Q CESC 15 51768825 51768825 + Missense_Mutation SNP C C G TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr15:51768825C>G c.6922G>C c.(6922-6924)Gaa>Caa p.E2308Q CESC 15 51768828 51768828 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr15:51768828C>T c.6919G>A c.(6919-6921)Gaa>Aaa p.E2307K CESC 15 51773272 51773272 + Missense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr15:51773272C>G c.6031G>C c.(6031-6033)Gat>Cat p.D2011H CESC 15 51778394 51778394 + Silent SNP G G A TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr15:51778394G>A c.5358C>T c.(5356-5358)ttC>ttT p.F1786F CESC 15 51790822 51790822 + Silent SNP G G A TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr15:51790822G>A c.4599C>T c.(4597-4599)ttC>ttT p.F1533F CESC 15 51828558 51828558 + Missense_Mutation SNP G G C TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr15:51828558G>C c.2119C>G c.(2119-2121)Ctt>Gtt p.L707V CESC 15 51857317 51857317 + Missense_Mutation SNP G G A TCGA-LP-A7HU-01A-11D-A33O-09 TCGA-LP-A7HU-10A-01D-A33O-09 g.chr15:51857317G>A c.332C>T c.(331-333)tCt>tTt p.S111F CESC 15 51868299 51868299 + Missense_Mutation SNP C C G TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr15:51868299C>G c.167G>C c.(166-168)gGa>gCa p.G56A CHOL 15 51741202 51741202 + Missense_Mutation SNP G G T TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr15:51741202G>T c.9090C>A c.(9088-9090)aaC>aaA p.N3030K CHOL 15 51766722 51766722 + Silent SNP C C T TCGA-YR-A95A-01A-12D-A417-09 TCGA-YR-A95A-10A-01D-A41A-09 g.chr15:51766722C>T c.7029G>A c.(7027-7029)ttG>ttA p.L2343L CHOL 15 51778485 51778485 + Missense_Mutation SNP C C T TCGA-ZH-A8Y6-01A-11D-A417-09 TCGA-ZH-A8Y6-10A-01D-A41A-09 g.chr15:51778485C>T c.5267G>A c.(5266-5268)cGt>cAt p.R1756H CHOL 15 51780309 51780309 + Missense_Mutation SNP G G T TCGA-W5-AA30-01A-31D-A417-09 TCGA-W5-AA30-10A-01D-A41A-09 g.chr15:51780309G>T c.5059C>A c.(5059-5061)Cat>Aat p.H1687N CHOL 15 51809289 51809289 + Missense_Mutation SNP C C T TCGA-3X-AAV9-01A-72D-A417-09 TCGA-3X-AAV9-10A-01D-A41A-09 g.chr15:51809289C>T c.2512G>A c.(2512-2514)Gca>Aca p.A838T COAD 15 51747414 51747414 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr15:51747414C>T c.8472G>A c.(8470-8472)gcG>gcA p.A2824A COAD 15 51749621 51749621 + Silent SNP A A G TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr15:51749621A>G c.8175T>C c.(8173-8175)taT>taC p.Y2725Y COAD 15 51750763 51750763 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51750763G>T c.8072C>A c.(8071-8073)tCt>tAt p.S2691Y COAD 15 51766596 51766596 + Frame_Shift_Del DEL A A - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr15:51766596delA c.7155delT c.(7153-7155)tttfs p.F2385fs COAD 15 51766615 51766615 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51766615C>T c.7136G>A c.(7135-7137)cGa>cAa p.R2379Q COAD 15 51766616 51766616 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51766616G>A c.7135C>T c.(7135-7137)Cga>Tga p.R2379* COAD 15 51766705 51766705 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51766705A>G c.7046T>C c.(7045-7047)gTt>gCt p.V2349A COAD 15 51766772 51766772 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:51766772T>G c.6979A>C c.(6979-6981)Aat>Cat p.N2327H COAD 15 51772872 51772872 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr15:51772872C>T c.6431G>A c.(6430-6432)cGa>cAa p.R2144Q COAD 15 51772926 51772926 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51772926C>T c.6377G>A c.(6376-6378)cGc>cAc p.R2126H COAD 15 51773461 51773461 + Missense_Mutation SNP A A G TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr15:51773461A>G c.5842T>C c.(5842-5844)Tct>Cct p.S1948P COAD 15 51778315 51778315 + Missense_Mutation SNP C C T TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr15:51778315C>T c.5437G>A c.(5437-5439)Gac>Aac p.D1813N COAD 15 51780207 51780207 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:51780207A>G c.5161T>C c.(5161-5163)Ttt>Ctt p.F1721L COAD 15 51780284 51780284 + Frame_Shift_Del DEL A A - TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr15:51780284delA c.5084delT c.(5083-5085)ttcfs p.F1695fs COAD 15 51783802 51783802 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51783802A>C c.4926T>G c.(4924-4926)atT>atG p.I1642M COAD 15 51783889 51783889 + Silent SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51783889C>A c.4839G>T c.(4837-4839)ctG>ctT p.L1613L COAD 15 51790932 51790932 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51790932T>G c.4489A>C c.(4489-4491)Aat>Cat p.N1497H COAD 15 51791307 51791307 + Missense_Mutation SNP C C A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr15:51791307C>A c.4114G>T c.(4114-4116)Gta>Tta p.V1372L COAD 15 51791395 51791395 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:51791395A>G c.4026T>C c.(4024-4026)ccT>ccC p.P1342P COAD 15 51791627 51791627 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:51791627T>C c.3794A>G c.(3793-3795)gAt>gGt p.D1265G COAD 15 51791933 51791933 + Missense_Mutation SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr15:51791933G>A c.3488C>T c.(3487-3489)cCg>cTg p.P1163L COAD 15 51792098 51792098 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:51792098T>G c.3323A>C c.(3322-3324)gAa>gCa p.E1108A COAD 15 51792126 51792126 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51792126C>A c.3295G>T c.(3295-3297)Gaa>Taa p.E1099* COAD 15 51792233 51792233 + Missense_Mutation SNP C C T TCGA-AA-3869-01A-01W-0995-10 TCGA-AA-3869-10A-01W-0995-10 g.chr15:51792233C>T c.3188G>A c.(3187-3189)aGt>aAt p.S1063N COAD 15 51792348 51792348 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:51792348G>T c.3073C>A c.(3073-3075)Cgc>Agc p.R1025S COAD 15 51795014 51795014 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:51795014G>A c.2981C>T c.(2980-2982)aCg>aTg p.T994M COAD 15 51795023 51795023 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:51795023A>G c.2972T>C c.(2971-2973)aTa>aCa p.I991T COAD 15 51795175 51795175 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:51795175C>A c.2820G>T c.(2818-2820)aaG>aaT p.K940N COAD 15 51799364 51799364 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:51799364G>A c.2731C>T c.(2731-2733)Cac>Tac p.H911Y COAD 15 51809275 51809275 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51809275T>G c.2526A>C c.(2524-2526)caA>caC p.Q842H COAD 15 51809289 51809289 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:51809289C>T c.2512G>A c.(2512-2514)Gca>Aca p.A838T COAD 15 51809289 51809289 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:51809289C>T c.2512G>A c.(2512-2514)Gca>Aca p.A838T COAD 15 51827950 51827950 + Silent SNP A A G TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr15:51827950A>G c.2346T>C c.(2344-2346)ttT>ttC p.F782F COAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-AZ-4323-01A-21D-1835-10 TCGA-AZ-4323-10A-01D-1835-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COAD 15 51828437 51828437 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51828437C>T c.2240G>A c.(2239-2241)cGa>cAa p.R747Q COAD 15 51828909 51828909 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51828909G>A c.1768C>T c.(1768-1770)Cac>Tac p.H590Y COAD 15 51828932 51828932 + Missense_Mutation SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:51828932T>C c.1745A>G c.(1744-1746)gAg>gGg p.E582G COAD 15 51828933 51828933 + Missense_Mutation SNP C C T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr15:51828933C>T c.1744G>A c.(1744-1746)Gag>Aag p.E582K COAD 15 51828974 51828974 + Missense_Mutation SNP A A T TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr15:51828974A>T c.1703T>A c.(1702-1704)aTa>aAa p.I568K COAD 15 51829785 51829785 + Missense_Mutation SNP G G T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:51829785G>T c.1517C>A c.(1516-1518)cCt>cAt p.P506H COAD 15 51829812 51829812 + Missense_Mutation SNP G G A TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr15:51829812G>A c.1490C>T c.(1489-1491)aCg>aTg p.T497M COAD 15 51829839 51829839 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr15:51829839G>A c.1463C>T c.(1462-1464)aCg>aTg p.T488M COAD 15 51829847 51829847 + Silent SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr15:51829847T>C c.1455A>G c.(1453-1455)ccA>ccG p.P485P COAD 15 51829847 51829847 + Silent SNP T T C TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr15:51829847T>C c.1455A>G c.(1453-1455)ccA>ccG p.P485P COAD 15 51829848 51829848 + Missense_Mutation SNP G G A TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr15:51829848G>A c.1454C>T c.(1453-1455)cCa>cTa p.P485L COAD 15 51830542 51830542 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:51830542C>T c.1213G>A c.(1213-1215)Gaa>Aaa p.E405K COAD 15 51834582 51834582 + Silent SNP A A G TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:51834582A>G c.1053T>C c.(1051-1053)caT>caC p.H351H COAD 15 51839448 51839448 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51839448T>G c.725A>C c.(724-726)aAa>aCa p.K242T COAD 15 51839455 51839455 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr15:51839455A>G c.718T>C c.(718-720)Tgg>Cgg p.W240R COAD 15 51857322 51857323 + Frame_Shift_Ins INS - - A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr15:51857322_51857323insA c.326_327insT c.(325-327)ttgfs p.L109fs COAD 15 51860691 51860691 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:51860691C>A c.278G>T c.(277-279)aGa>aTa p.R93I COAD 15 51860704 51860704 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51860704T>G c.265A>C c.(265-267)Aat>Cat p.N89H COAD 15 51860704 51860704 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51860704T>G c.265A>C c.(265-267)Aat>Cat p.N89H COADREAD 15 51747414 51747414 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr15:51747414C>T c.8472G>A c.(8470-8472)gcG>gcA p.A2824A COADREAD 15 51749621 51749621 + Silent SNP A A G TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr15:51749621A>G c.8175T>C c.(8173-8175)taT>taC p.Y2725Y COADREAD 15 51750763 51750763 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51750763G>T c.8072C>A c.(8071-8073)tCt>tAt p.S2691Y COADREAD 15 51766596 51766596 + Frame_Shift_Del DEL A A - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr15:51766596delA c.7155delT c.(7153-7155)tttfs p.F2385fs COADREAD 15 51766615 51766615 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51766615C>T c.7136G>A c.(7135-7137)cGa>cAa p.R2379Q COADREAD 15 51766616 51766616 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51766616G>A c.7135C>T c.(7135-7137)Cga>Tga p.R2379* COADREAD 15 51766705 51766705 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51766705A>G c.7046T>C c.(7045-7047)gTt>gCt p.V2349A COADREAD 15 51766772 51766772 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:51766772T>G c.6979A>C c.(6979-6981)Aat>Cat p.N2327H COADREAD 15 51772872 51772872 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr15:51772872C>T c.6431G>A c.(6430-6432)cGa>cAa p.R2144Q COADREAD 15 51772926 51772926 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51772926C>T c.6377G>A c.(6376-6378)cGc>cAc p.R2126H COADREAD 15 51773461 51773461 + Missense_Mutation SNP A A G TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr15:51773461A>G c.5842T>C c.(5842-5844)Tct>Cct p.S1948P COADREAD 15 51778315 51778315 + Missense_Mutation SNP C C T TCGA-AA-3842-01A-01W-0995-10 TCGA-AA-3842-10A-01W-0995-10 g.chr15:51778315C>T c.5437G>A c.(5437-5439)Gac>Aac p.D1813N COADREAD 15 51780207 51780207 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:51780207A>G c.5161T>C c.(5161-5163)Ttt>Ctt p.F1721L COADREAD 15 51780284 51780284 + Frame_Shift_Del DEL A A - TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr15:51780284delA c.5084delT c.(5083-5085)ttcfs p.F1695fs COADREAD 15 51783802 51783802 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51783802A>C c.4926T>G c.(4924-4926)atT>atG p.I1642M COADREAD 15 51783889 51783889 + Silent SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:51783889C>A c.4839G>T c.(4837-4839)ctG>ctT p.L1613L COADREAD 15 51790932 51790932 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51790932T>G c.4489A>C c.(4489-4491)Aat>Cat p.N1497H COADREAD 15 51791231 51791231 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51791231C>T c.4190G>A c.(4189-4191)cGa>cAa p.R1397Q COADREAD 15 51791307 51791307 + Missense_Mutation SNP C C A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr15:51791307C>A c.4114G>T c.(4114-4116)Gta>Tta p.V1372L COADREAD 15 51791395 51791395 + Silent SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:51791395A>G c.4026T>C c.(4024-4026)ccT>ccC p.P1342P COADREAD 15 51791627 51791627 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:51791627T>C c.3794A>G c.(3793-3795)gAt>gGt p.D1265G COADREAD 15 51791933 51791933 + Missense_Mutation SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr15:51791933G>A c.3488C>T c.(3487-3489)cCg>cTg p.P1163L COADREAD 15 51792098 51792098 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:51792098T>G c.3323A>C c.(3322-3324)gAa>gCa p.E1108A COADREAD 15 51792126 51792126 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51792126C>A c.3295G>T c.(3295-3297)Gaa>Taa p.E1099* COADREAD 15 51792233 51792233 + Missense_Mutation SNP C C T TCGA-AA-3869-01A-01W-0995-10 TCGA-AA-3869-10A-01W-0995-10 g.chr15:51792233C>T c.3188G>A c.(3187-3189)aGt>aAt p.S1063N COADREAD 15 51792348 51792348 + Missense_Mutation SNP G G T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:51792348G>T c.3073C>A c.(3073-3075)Cgc>Agc p.R1025S COADREAD 15 51795011 51795011 + Missense_Mutation SNP G G T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr15:51795011G>T c.2984C>A c.(2983-2985)cCt>cAt p.P995H COADREAD 15 51795014 51795014 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:51795014G>A c.2981C>T c.(2980-2982)aCg>aTg p.T994M COADREAD 15 51795023 51795023 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:51795023A>G c.2972T>C c.(2971-2973)aTa>aCa p.I991T COADREAD 15 51795175 51795175 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:51795175C>A c.2820G>T c.(2818-2820)aaG>aaT p.K940N COADREAD 15 51799364 51799364 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr15:51799364G>A c.2731C>T c.(2731-2733)Cac>Tac p.H911Y COADREAD 15 51806663 51806663 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51806663C>A c.2620G>T c.(2620-2622)Gaa>Taa p.E874* COADREAD 15 51809275 51809275 + Splice_Site SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51809275T>G c.2526A>C c.(2524-2526)caA>caC p.Q842H COADREAD 15 51809289 51809289 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr15:51809289C>T c.2512G>A c.(2512-2514)Gca>Aca p.A838T COADREAD 15 51809289 51809289 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:51809289C>T c.2512G>A c.(2512-2514)Gca>Aca p.A838T COADREAD 15 51827950 51827950 + Silent SNP A A G TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr15:51827950A>G c.2346T>C c.(2344-2346)ttT>ttC p.F782F COADREAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COADREAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-AZ-4323-01A-21D-1835-10 TCGA-AZ-4323-10A-01D-1835-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COADREAD 15 51827952 51827952 + Missense_Mutation SNP A A G TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr15:51827952A>G c.2344T>C c.(2344-2346)Ttt>Ctt p.F782L COADREAD 15 51828437 51828437 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51828437C>T c.2240G>A c.(2239-2241)cGa>cAa p.R747Q COADREAD 15 51828668 51828668 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51828668T>G c.2009A>C c.(2008-2010)cAt>cCt p.H670P COADREAD 15 51828909 51828909 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51828909G>A c.1768C>T c.(1768-1770)Cac>Tac p.H590Y COADREAD 15 51828932 51828932 + Missense_Mutation SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:51828932T>C c.1745A>G c.(1744-1746)gAg>gGg p.E582G COADREAD 15 51828933 51828933 + Missense_Mutation SNP C C T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr15:51828933C>T c.1744G>A c.(1744-1746)Gag>Aag p.E582K COADREAD 15 51828974 51828974 + Missense_Mutation SNP A A T TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr15:51828974A>T c.1703T>A c.(1702-1704)aTa>aAa p.I568K COADREAD 15 51829785 51829785 + Missense_Mutation SNP G G T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:51829785G>T c.1517C>A c.(1516-1518)cCt>cAt p.P506H COADREAD 15 51829812 51829812 + Missense_Mutation SNP G G A TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr15:51829812G>A c.1490C>T c.(1489-1491)aCg>aTg p.T497M COADREAD 15 51829839 51829839 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr15:51829839G>A c.1463C>T c.(1462-1464)aCg>aTg p.T488M COADREAD 15 51829847 51829847 + Silent SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr15:51829847T>C c.1455A>G c.(1453-1455)ccA>ccG p.P485P COADREAD 15 51829847 51829847 + Silent SNP T T C TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr15:51829847T>C c.1455A>G c.(1453-1455)ccA>ccG p.P485P COADREAD 15 51829848 51829848 + Missense_Mutation SNP G G A TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr15:51829848G>A c.1454C>T c.(1453-1455)cCa>cTa p.P485L COADREAD 15 51829848 51829848 + Missense_Mutation SNP G G T TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr15:51829848G>T c.1454C>A c.(1453-1455)cCa>cAa p.P485Q COADREAD 15 51830542 51830542 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:51830542C>T c.1213G>A c.(1213-1215)Gaa>Aaa p.E405K COADREAD 15 51834582 51834582 + Silent SNP A A G TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:51834582A>G c.1053T>C c.(1051-1053)caT>caC p.H351H COADREAD 15 51839448 51839448 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51839448T>G c.725A>C c.(724-726)aAa>aCa p.K242T COADREAD 15 51839455 51839455 + Missense_Mutation SNP A A G TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr15:51839455A>G c.718T>C c.(718-720)Tgg>Cgg p.W240R COADREAD 15 51839564 51839564 + Nonsense_Mutation SNP C C T TCGA-AG-3878-01A-02W-0899-10 TCGA-AG-3878-10A-01W-0901-10 g.chr15:51839564C>T c.609G>A c.(607-609)tgG>tgA p.W203* COADREAD 15 51857322 51857323 + Frame_Shift_Ins INS - - A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr15:51857322_51857323insA c.326_327insT c.(325-327)ttgfs p.L109fs COADREAD 15 51860691 51860691 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:51860691C>A c.278G>T c.(277-279)aGa>aTa p.R93I COADREAD 15 51860704 51860704 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:51860704T>G c.265A>C c.(265-267)Aat>Cat p.N89H COADREAD 15 51860704 51860704 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:51860704T>G c.265A>C c.(265-267)Aat>Cat p.N89H ESCA 15 51742397 51742397 + Missense_Mutation SNP C C T TCGA-R6-A8WG-01A-11D-A37C-09 TCGA-R6-A8WG-10A-01D-A37F-09 g.chr15:51742397C>T c.8830G>A c.(8830-8832)Gct>Act p.A2944T ESCA 15 51742484 51742484 + Missense_Mutation SNP G G T TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr15:51742484G>T c.8743C>A c.(8743-8745)Cta>Ata p.L2915I ESCA 15 51763434 51763434 + Missense_Mutation SNP A A C TCGA-L5-A4OR-01A-11D-A27G-09 TCGA-L5-A4OR-11A-11D-A27G-09 g.chr15:51763434A>C c.7375T>G c.(7375-7377)Tat>Gat p.Y2459D ESCA 15 51773127 51773127 + Missense_Mutation SNP G G T TCGA-VR-AA4G-01A-11D-A37C-09 TCGA-VR-AA4G-10A-01D-A37F-09 g.chr15:51773127G>T c.6176C>A c.(6175-6177)gCt>gAt p.A2059D ESCA 15 51773255 51773255 + Missense_Mutation SNP G G T TCGA-R6-A6DN-01B-11D-A31U-09 TCGA-R6-A6DN-10A-01D-A31U-09 g.chr15:51773255G>T c.6048C>A c.(6046-6048)gaC>gaA p.D2016E ESCA 15 51787281 51787281 + Missense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:51787281G>T c.4723C>A c.(4723-4725)Cta>Ata p.L1575I ESCA 15 51791379 51791379 + Missense_Mutation SNP G G A TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr15:51791379G>A c.4042C>T c.(4042-4044)Cat>Tat p.H1348Y ESCA 15 51828604 51828604 + Silent SNP T T C TCGA-R6-A8WG-01A-11D-A37C-09 TCGA-R6-A8WG-10A-01D-A37F-09 g.chr15:51828604T>C c.2073A>G c.(2071-2073)agA>agG p.R691R ESCA 15 51839582 51839582 + Nonsense_Mutation SNP C C T TCGA-R6-A8WC-01A-11D-A37C-09 TCGA-R6-A8WC-10A-01D-A37F-09 g.chr15:51839582C>T c.591G>A c.(589-591)tgG>tgA p.W197* ESCA 15 51857295 51857295 + Missense_Mutation SNP C C G TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr15:51857295C>G c.354G>C c.(352-354)tgG>tgC p.W118C ESCA 15 51860757 51860758 + Splice_Site INS - - A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:51860757_51860758insA c.e3-2 GBMLGG 15 51750758 51750758 + Missense_Mutation SNP G G C TCGA-E1-A7YI-01A-11D-A34A-08 TCGA-E1-A7YI-10A-01D-A34A-08 g.chr15:51750758G>C c.8077C>G c.(8077-8079)Ctg>Gtg p.L2693V GBMLGG 15 51766595 51766595 + Missense_Mutation SNP C C T TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chr15:51766595C>T c.7156G>A c.(7156-7158)Gga>Aga p.G2386R GBMLGG 15 51772245 51772245 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:51772245A>G c.6656T>C c.(6655-6657)aTa>aCa p.I2219T GBMLGG 15 51772904 51772906 + In_Frame_Del DEL TCT TCT - TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr15:51772904_51772906delTCT c.6397_6399delAGA c.(6397-6399)agadel p.R2133del GBMLGG 15 51773679 51773679 + Missense_Mutation SNP T T C TCGA-DU-8165-01A-11D-2253-08 TCGA-DU-8165-10A-01D-2253-08 g.chr15:51773679T>C c.5624A>G c.(5623-5625)gAt>gGt p.D1875G GBMLGG 15 51791722 51791724 + In_Frame_Del DEL AAG AAG - TCGA-E1-5305-01A-01D-1893-08 TCGA-E1-5305-10A-01D-1893-08 g.chr15:51791722_51791724delAAG c.3697_3699delCTT c.(3697-3699)cttdel p.L1233del GBMLGG 15 51828821 51828821 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:51828821C>T c.1856G>A c.(1855-1857)gGt>gAt p.G619D HNSC 15 51741298 51741298 + Missense_Mutation SNP C C T TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr15:51741298C>T c.8994G>A c.(8992-8994)atG>atA p.M2998I HNSC 15 51741321 51741321 + Nonsense_Mutation SNP G G A TCGA-CQ-6227-01A-11D-1912-08 TCGA-CQ-6227-10A-01D-1912-08 g.chr15:51741321G>A c.8971C>T c.(8971-8973)Cga>Tga p.R2991* HNSC 15 51743860 51743860 + Missense_Mutation SNP C C T TCGA-D6-A6EN-01A-11D-A31L-08 TCGA-D6-A6EN-10A-01D-A31J-08 g.chr15:51743860C>T c.8665G>A c.(8665-8667)Gga>Aga p.G2889R HNSC 15 51757808 51757808 + Missense_Mutation SNP G G A TCGA-CN-4738-01A-02D-1512-08 TCGA-CN-4738-10A-01D-1512-08 g.chr15:51757808G>A c.7558C>T c.(7558-7560)Cac>Tac p.H2520Y HNSC 15 51763484 51763484 + Missense_Mutation SNP C C G TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr15:51763484C>G c.7325G>C c.(7324-7326)aGa>aCa p.R2442T HNSC 15 51772275 51772275 + Missense_Mutation SNP G G A TCGA-P3-A6T3-01A-11D-A34J-08 TCGA-P3-A6T3-10A-01D-A34M-08 g.chr15:51772275G>A c.6626C>T c.(6625-6627)tCa>tTa p.S2209L HNSC 15 51773096 51773096 + Silent SNP G G A TCGA-P3-A6SW-01A-11D-A34J-08 TCGA-P3-A6SW-10A-01D-A34M-08 g.chr15:51773096G>A c.6207C>T c.(6205-6207)ctC>ctT p.L2069L HNSC 15 51773152 51773152 + Missense_Mutation SNP G G T TCGA-CV-6951-01A-11D-1912-08 TCGA-CV-6951-10A-01D-1912-08 g.chr15:51773152G>T c.6151C>A c.(6151-6153)Ctt>Att p.L2051I HNSC 15 51773320 51773320 + Missense_Mutation SNP C C G TCGA-P3-A6T6-01A-11D-A34J-08 TCGA-P3-A6T6-10A-01D-A34M-08 g.chr15:51773320C>G c.5983G>C c.(5983-5985)Ggt>Cgt p.G1995R HNSC 15 51778300 51778300 + Missense_Mutation SNP G G C TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr15:51778300G>C c.5452C>G c.(5452-5454)Caa>Gaa p.Q1818E HNSC 15 51787314 51787314 + Missense_Mutation SNP C C T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr15:51787314C>T c.4690G>A c.(4690-4692)Gag>Aag p.E1564K HNSC 15 51790872 51790872 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr15:51790872G>A c.4549C>T c.(4549-4551)Cat>Tat p.H1517Y HNSC 15 51791379 51791379 + Missense_Mutation SNP G G A TCGA-CN-A640-01A-21D-A30E-08 TCGA-CN-A640-10A-01D-A30H-08 g.chr15:51791379G>A c.4042C>T c.(4042-4044)Cat>Tat p.H1348Y HNSC 15 51791702 51791702 + Missense_Mutation SNP G G C TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr15:51791702G>C c.3719C>G c.(3718-3720)tCt>tGt p.S1240C HNSC 15 51806663 51806663 + Missense_Mutation SNP C C G TCGA-BA-5556-01A-01D-1512-08 TCGA-BA-5556-10A-01D-1512-08 g.chr15:51806663C>G c.2620G>C c.(2620-2622)Gaa>Caa p.E874Q HNSC 15 51806687 51806687 + Missense_Mutation SNP C C T TCGA-UF-A7JA-01A-12D-A34J-08 TCGA-UF-A7JA-10A-01D-A34M-08 g.chr15:51806687C>T c.2596G>A c.(2596-2598)Gaa>Aaa p.E866K HNSC 15 51809332 51809332 + Silent SNP G G A TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr15:51809332G>A c.2469C>T c.(2467-2469)agC>agT p.S823S HNSC 15 51809333 51809333 + Missense_Mutation SNP C C T TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr15:51809333C>T c.2468G>A c.(2467-2469)aGc>aAc p.S823N HNSC 15 51828991 51828991 + Silent SNP G G A TCGA-UF-A7JA-01A-12D-A34J-08 TCGA-UF-A7JA-10A-01D-A34M-08 g.chr15:51828991G>A c.1686C>T c.(1684-1686)atC>atT p.I562I HNSC 15 51837835 51837835 + Missense_Mutation SNP G G T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr15:51837835G>T c.875C>A c.(874-876)gCc>gAc p.A292D HNSC 15 51914710 51914710 + Silent SNP G G A TCGA-UF-A71B-01A-12D-A34J-08 TCGA-UF-A71B-10B-01D-A34M-08 g.chr15:51914710G>A c.33C>T c.(31-33)gtC>gtT p.V11V KICH 15 51768854 51768854 + Missense_Mutation SNP C C A TCGA-KM-8438-01A-11D-2310-10 TCGA-KM-8438-10A-01D-2311-10 g.chr15:51768854C>A c.6893G>T c.(6892-6894)cGt>cTt p.R2298L KICH 15 51787229 51787229 + Missense_Mutation SNP A A G TCGA-KN-8418-01A-11D-2310-10 TCGA-KN-8418-11A-01D-2310-10 g.chr15:51787229A>G c.4775T>C c.(4774-4776)cTt>cCt p.L1592P KIPAN 15 51741365 51741365 + Missense_Mutation SNP A A G TCGA-B0-4852-01A-01D-1501-10 TCGA-B0-4852-11A-01D-1501-10 g.chr15:51741365A>G c.8927T>C c.(8926-8928)cTa>cCa p.L2976P KIPAN 15 51749533 51749533 + Missense_Mutation SNP C C A TCGA-2Z-A9J3-01A-12D-A382-10 TCGA-2Z-A9J3-10A-01D-A385-10 g.chr15:51749533C>A c.8263G>T c.(8263-8265)Gct>Tct p.A2755S KIPAN 15 51758502 51758502 + Missense_Mutation SNP G G A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr15:51758502G>A c.7396C>T c.(7396-7398)Ctt>Ttt p.L2466F KIPAN 15 51768854 51768854 + Missense_Mutation SNP C C A TCGA-KM-8438-01A-11D-2310-10 TCGA-KM-8438-10A-01D-2311-10 g.chr15:51768854C>A c.6893G>T c.(6892-6894)cGt>cTt p.R2298L KIPAN 15 51778458 51778458 + Nonsense_Mutation SNP G G T TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr15:51778458G>T c.5294C>A c.(5293-5295)tCa>tAa p.S1765* KIPAN 15 51778460 51778460 + Silent SNP A A G TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr15:51778460A>G c.5292T>C c.(5290-5292)acT>acC p.T1764T KIPAN 15 51783940 51783940 + Silent SNP G G A TCGA-UZ-A9Q1-01A-11D-A42J-10 TCGA-UZ-A9Q1-10A-01D-A42M-10 g.chr15:51783940G>A c.4788C>T c.(4786-4788)gtC>gtT p.V1596V KIPAN 15 51787229 51787229 + Missense_Mutation SNP A A G TCGA-KN-8418-01A-11D-2310-10 TCGA-KN-8418-11A-01D-2310-10 g.chr15:51787229A>G c.4775T>C c.(4774-4776)cTt>cCt p.L1592P KIPAN 15 51790800 51790800 + Missense_Mutation SNP C C A TCGA-CZ-4861-01A-01D-1373-10 TCGA-CZ-4861-11A-01D-1373-10 g.chr15:51790800C>A c.4621G>T c.(4621-4623)Gtg>Ttg p.V1541L KIPAN 15 51792075 51792075 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr15:51792075C>T c.3346G>A c.(3346-3348)Gag>Aag p.E1116K KIPAN 15 51799330 51799330 + Splice_Site SNP C C T TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr15:51799330C>T c.e16+1 KIPAN 15 51828461 51828461 + Missense_Mutation SNP G G C TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr15:51828461G>C c.2216C>G c.(2215-2217)aCt>aGt p.T739S KIPAN 15 51837940 51837940 + Nonsense_Mutation SNP A A C TCGA-A3-3370-01A-02D-1421-08 TCGA-A3-3370-11A-01D-1421-08 g.chr15:51837940A>C c.770T>G c.(769-771)tTa>tGa p.L257* KIPAN 15 51839582 51839582 + Missense_Mutation SNP C C G TCGA-B0-4852-01A-01D-1501-10 TCGA-B0-4852-11A-01D-1501-10 g.chr15:51839582C>G c.591G>C c.(589-591)tgG>tgC p.W197C KIPAN 15 51857284 51857284 + Splice_Site SNP C C A TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr15:51857284C>A c.e4+1 KIRC 15 51741365 51741365 + Missense_Mutation SNP A A G TCGA-B0-4852-01A-01D-1501-10 TCGA-B0-4852-11A-01D-1501-10 g.chr15:51741365A>G c.8927T>C c.(8926-8928)cTa>cCa p.L2976P KIRC 15 51778458 51778458 + Nonsense_Mutation SNP G G T TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr15:51778458G>T c.5294C>A c.(5293-5295)tCa>tAa p.S1765* KIRC 15 51778460 51778460 + Silent SNP A A G TCGA-B0-5709-01A-11D-1534-10 TCGA-B0-5709-11A-01D-1534-10 g.chr15:51778460A>G c.5292T>C c.(5290-5292)acT>acC p.T1764T KIRC 15 51790800 51790800 + Missense_Mutation SNP C C A TCGA-CZ-4861-01A-01D-1373-10 TCGA-CZ-4861-11A-01D-1373-10 g.chr15:51790800C>A c.4621G>T c.(4621-4623)Gtg>Ttg p.V1541L KIRC 15 51828461 51828461 + Missense_Mutation SNP G G C TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr15:51828461G>C c.2216C>G c.(2215-2217)aCt>aGt p.T739S KIRC 15 51837940 51837940 + Nonsense_Mutation SNP A A C TCGA-A3-3370-01A-02D-1421-08 TCGA-A3-3370-11A-01D-1421-08 g.chr15:51837940A>C c.770T>G c.(769-771)tTa>tGa p.L257* KIRC 15 51839582 51839582 + Missense_Mutation SNP C C G TCGA-B0-4852-01A-01D-1501-10 TCGA-B0-4852-11A-01D-1501-10 g.chr15:51839582C>G c.591G>C c.(589-591)tgG>tgC p.W197C KIRP 15 51749533 51749533 + Missense_Mutation SNP C C A TCGA-2Z-A9J3-01A-12D-A382-10 TCGA-2Z-A9J3-10A-01D-A385-10 g.chr15:51749533C>A c.8263G>T c.(8263-8265)Gct>Tct p.A2755S KIRP 15 51758502 51758502 + Missense_Mutation SNP G G A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr15:51758502G>A c.7396C>T c.(7396-7398)Ctt>Ttt p.L2466F KIRP 15 51783940 51783940 + Silent SNP G G A TCGA-UZ-A9Q1-01A-11D-A42J-10 TCGA-UZ-A9Q1-10A-01D-A42M-10 g.chr15:51783940G>A c.4788C>T c.(4786-4788)gtC>gtT p.V1596V KIRP 15 51792075 51792075 + Missense_Mutation SNP C C T TCGA-GL-A9DE-01A-11D-A36X-10 TCGA-GL-A9DE-10A-01D-A370-10 g.chr15:51792075C>T c.3346G>A c.(3346-3348)Gag>Aag p.E1116K KIRP 15 51799330 51799330 + Splice_Site SNP C C T TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr15:51799330C>T c.e16+1 KIRP 15 51857284 51857284 + Splice_Site SNP C C A TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr15:51857284C>A c.e4+1 LGG 15 51750758 51750758 + Missense_Mutation SNP G G C TCGA-E1-A7YI-01A-11D-A34A-08 TCGA-E1-A7YI-10A-01D-A34A-08 g.chr15:51750758G>C c.8077C>G c.(8077-8079)Ctg>Gtg p.L2693V LGG 15 51766595 51766595 + Missense_Mutation SNP C C T TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chr15:51766595C>T c.7156G>A c.(7156-7158)Gga>Aga p.G2386R LGG 15 51772245 51772245 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:51772245A>G c.6656T>C c.(6655-6657)aTa>aCa p.I2219T LGG 15 51772904 51772906 + In_Frame_Del DEL TCT TCT - TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr15:51772904_51772906delTCT c.6397_6399delAGA c.(6397-6399)agadel p.R2133del LGG 15 51773679 51773679 + Missense_Mutation SNP T T C TCGA-DU-8165-01A-11D-2253-08 TCGA-DU-8165-10A-01D-2253-08 g.chr15:51773679T>C c.5624A>G c.(5623-5625)gAt>gGt p.D1875G LGG 15 51791722 51791724 + In_Frame_Del DEL AAG AAG - TCGA-E1-5305-01A-01D-1893-08 TCGA-E1-5305-10A-01D-1893-08 g.chr15:51791722_51791724delAAG c.3697_3699delCTT c.(3697-3699)cttdel p.L1233del LGG 15 51828821 51828821 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:51828821C>T c.1856G>A c.(1855-1857)gGt>gAt p.G619D LIHC 15 51748508 51748508 + Missense_Mutation SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr15:51748508T>C c.8330A>G c.(8329-8331)tAc>tGc p.Y2777C LIHC 15 51756896 51756896 + Missense_Mutation SNP A A C TCGA-BW-A5NQ-01A-11D-A27I-10 TCGA-BW-A5NQ-10A-01D-A27I-10 g.chr15:51756896A>C c.7781T>G c.(7780-7782)cTa>cGa p.L2594R LIHC 15 51766616 51766616 + Silent SNP G G T TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr15:51766616G>T c.7135C>A c.(7135-7137)Cga>Aga p.R2379R LIHC 15 51768790 51768790 + Frame_Shift_Del DEL C C - TCGA-DD-AACF-01A-11D-A40R-10 TCGA-DD-AACF-10A-01D-A40U-10 g.chr15:51768790delC c.6957delG c.(6955-6957)tggfs p.W2319fs LIHC 15 51772972 51772972 + Missense_Mutation SNP C C G TCGA-DD-AADO-01A-11D-A40R-10 TCGA-DD-AADO-10A-01D-A40U-10 g.chr15:51772972C>G c.6331G>C c.(6331-6333)Gat>Cat p.D2111H LIHC 15 51791589 51791589 + Missense_Mutation SNP C C G TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr15:51791589C>G c.3832G>C c.(3832-3834)Gtc>Ctc p.V1278L LIHC 15 51791589 51791589 + Missense_Mutation SNP C C G TCGA-DD-A1EL-01A-11D-A152-10 TCGA-DD-A1EL-10A-01D-A152-10 g.chr15:51791589C>G c.3832G>C c.(3832-3834)Gtc>Ctc p.V1278L LIHC 15 51828802 51828802 + Silent SNP T T A TCGA-CC-5259-01A-31D-A20W-10 TCGA-CC-5259-10A-01D-A20W-10 g.chr15:51828802T>A c.1875A>T c.(1873-1875)gcA>gcT p.A625A LIHC 15 51839582 51839582 + Nonsense_Mutation SNP C C T TCGA-DD-A3A7-01A-11D-A22F-10 TCGA-DD-A3A7-11A-11D-A22F-10 g.chr15:51839582C>T c.591G>A c.(589-591)tgG>tgA p.W197* LIHC 15 51860705 51860705 + Silent SNP T T A TCGA-DD-AAW1-01A-11D-A40P-10 TCGA-DD-AAW1-10A-01D-A40P-10 g.chr15:51860705T>A c.264A>T c.(262-264)atA>atT p.I88I LIHC 15 51914662 51914662 + Frame_Shift_Del DEL G G - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr15:51914662delG c.81delC c.(79-81)cccfs p.P27fs LUAD 15 51741321 51741321 + Nonsense_Mutation SNP G G A TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr15:51741321G>A c.8971C>T c.(8971-8973)Cga>Tga p.R2991* LUAD 15 51741321 51741321 + Nonsense_Mutation SNP G G A TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr15:51741321G>A c.8971C>T c.(8971-8973)Cga>Tga p.R2991* LUAD 15 51741341 51741341 + Missense_Mutation SNP T T A TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr15:51741341T>A c.8951A>T c.(8950-8952)cAt>cTt p.H2984L LUAD 15 51743895 51743895 + Splice_Site SNP C C G TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr15:51743895C>G c.e41-1 LUAD 15 51755682 51755682 + Missense_Mutation SNP G G A TCGA-75-6211-01A-11D-1753-08 TCGA-75-6211-10A-01D-1753-08 g.chr15:51755682G>A c.7817C>T c.(7816-7818)tCt>tTt p.S2606F LUAD 15 51756966 51756966 + Missense_Mutation SNP A A C TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr15:51756966A>C c.7711T>G c.(7711-7713)Tat>Gat p.Y2571D LUAD 15 51772810 51772810 + Missense_Mutation SNP G G A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr15:51772810G>A c.6493C>T c.(6493-6495)Cat>Tat p.H2165Y LUAD 15 51780177 51780177 + Missense_Mutation SNP C C A TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr15:51780177C>A c.5191G>T c.(5191-5193)Gct>Tct p.A1731S LUAD 15 51780775 51780775 + Missense_Mutation SNP T T C TCGA-35-4123-01A-01D-1105-08 TCGA-35-4123-10A-01D-1105-08 g.chr15:51780775T>C c.5021A>G c.(5020-5022)aAg>aGg p.K1674R LUAD 15 51791155 51791155 + Silent SNP C C T TCGA-97-8176-01A-11D-2393-08 TCGA-97-8176-10B-01D-2393-08 g.chr15:51791155C>T c.4266G>A c.(4264-4266)gaG>gaA p.E1422E LUAD 15 51791717 51791717 + Missense_Mutation SNP G G T TCGA-73-7499-01A-11D-2184-08 TCGA-73-7499-10A-01D-2184-08 g.chr15:51791717G>T c.3704C>A c.(3703-3705)tCt>tAt p.S1235Y LUAD 15 51792347 51792347 + Missense_Mutation SNP C C T TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr15:51792347C>T c.3074G>A c.(3073-3075)cGc>cAc p.R1025H LUAD 15 51792375 51792375 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr15:51792375C>A c.3046G>T c.(3046-3048)Gtt>Ttt p.V1016F LUAD 15 51830521 51830521 + Nonsense_Mutation SNP G G A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr15:51830521G>A c.1234C>T c.(1234-1236)Cga>Tga p.R412* LUAD 15 51834664 51834664 + Missense_Mutation SNP C C A TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr15:51834664C>A c.971G>T c.(970-972)aGg>aTg p.R324M LUAD 15 51837821 51837821 + Missense_Mutation SNP G G A TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr15:51837821G>A c.889C>T c.(889-891)Cat>Tat p.H297Y LUAD 15 51855592 51855592 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr15:51855592C>A c.553G>T c.(553-555)Gct>Tct p.A185S LUAD 15 51856388 51856388 + Missense_Mutation SNP T T A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr15:51856388T>A c.434A>T c.(433-435)gAg>gTg p.E145V LUAD 15 51860697 51860697 + Missense_Mutation SNP T T A TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chr15:51860697T>A c.272A>T c.(271-273)cAt>cTt p.H91L LUSC 15 51750748 51750748 + Missense_Mutation SNP T T A TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr15:51750748T>A c.8087A>T c.(8086-8088)cAg>cTg p.Q2696L LUSC 15 51755631 51755631 + Missense_Mutation SNP A A G TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr15:51755631A>G c.7868T>C c.(7867-7869)gTc>gCc p.V2623A LUSC 15 51757049 51757049 + Missense_Mutation SNP C C A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr15:51757049C>A c.7628G>T c.(7627-7629)gGt>gTt p.G2543V LUSC 15 51792045 51792045 + Missense_Mutation SNP C C T TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr15:51792045C>T c.3376G>A c.(3376-3378)Gat>Aat p.D1126N LUSC 15 51828679 51828679 + Missense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr15:51828679C>G c.1998G>C c.(1996-1998)ttG>ttC p.L666F LUSC 15 51828946 51828946 + Silent SNP C C A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr15:51828946C>A c.1731G>T c.(1729-1731)acG>acT p.T577T LUSC 15 51828999 51828999 + Missense_Mutation SNP T T C TCGA-56-1622-01A-01D-1521-08 TCGA-56-1622-11A-01D-1521-08 g.chr15:51828999T>C c.1678A>G c.(1678-1680)Aaa>Gaa p.K560E LUSC 15 51830482 51830483 + Missense_Mutation DNP CA CA AC TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr15:51830482_51830483CA>AC c.1272_1273TG>GT c.(1270-1275)gaTGat>gaGTat p.424_425DD>EY LUSC 15 51839432 51839432 + Missense_Mutation SNP C C A TCGA-22-5471-01A-01D-1632-08 TCGA-22-5471-11A-01D-1632-08 g.chr15:51839432C>A c.741G>T c.(739-741)atG>atT p.M247I LUSC 15 51839475 51839475 + Missense_Mutation SNP C C T TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr15:51839475C>T c.698G>A c.(697-699)cGa>cAa p.R233Q OV 15 51741380 51741380 + Missense_Mutation SNP A A C TCGA-29-1768-01A-01W-0633-09 TCGA-29-1768-10A-01W-0634-09 g.chr15:51741380A>C c.8912T>G c.(8911-8913)tTg>tGg p.L2971W OV 15 51742416 51742416 + Silent SNP C C T TCGA-29-1710-01A-02W-0633-09 TCGA-29-1710-10A-01W-0633-09 g.chr15:51742416C>T c.8811G>A c.(8809-8811)acG>acA p.T2937T OV 15 51773448 51773448 + Nonsense_Mutation SNP C C T TCGA-13-2071-01A-02D-1526-09 TCGA-13-2071-10A-01D-1526-09 g.chr15:51773448C>T c.5855G>A c.(5854-5856)tGg>tAg p.W1952* OV 15 51791851 51791851 + Missense_Mutation SNP A A T TCGA-24-1567-01A-01W-0615-10 TCGA-24-1567-10A-01W-0615-10 g.chr15:51791851A>T c.3570T>A c.(3568-3570)aaT>aaA p.N1190K OV 15 51795104 51795104 + Missense_Mutation SNP A A G TCGA-23-1124-01A-01W-0488-09 TCGA-23-1124-10A-01W-0488-09 g.chr15:51795104A>G c.2891T>C c.(2890-2892)cTt>cCt p.L964P OV 15 51799402 51799402 + Missense_Mutation SNP T T A TCGA-13-2061-01A-01D-1526-09 TCGA-13-2061-10A-01D-1526-09 g.chr15:51799402T>A c.2693A>T c.(2692-2694)gAg>gTg p.E898V OV 15 51827951 51827951 + Missense_Mutation SNP A A G TCGA-04-1343-01A-01W-0488-09 TCGA-04-1343-10A-01W-0489-09 g.chr15:51827951A>G c.2345T>C c.(2344-2346)tTt>tCt p.F782S OV 15 51828931 51828931 + Missense_Mutation SNP C C G TCGA-59-2351-01A-01W-0799-08 TCGA-59-2351-10A-01W-0800-08 g.chr15:51828931C>G c.1746G>C c.(1744-1746)gaG>gaC p.E582D OV 15 51828974 51828974 + Missense_Mutation SNP A A C TCGA-09-2056-01B-01W-0722-08 TCGA-09-2056-11A-01W-0722-08 g.chr15:51828974A>C c.1703T>G c.(1702-1704)aTa>aGa p.I568R OV 15 51829060 51829060 + Splice_Site SNP C C A TCGA-29-1696-01A-01W-0633-09 TCGA-29-1696-10A-01W-0633-09 g.chr15:51829060C>A c.e12-1 OV 15 51829847 51829847 + Silent SNP T T G TCGA-24-1563-01A-01W-0553-09 TCGA-24-1563-10A-01W-0553-09 g.chr15:51829847T>G c.1455A>C c.(1453-1455)ccA>ccC p.P485P PAAD 15 51750948 51750948 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:51750948G>T c.7968C>A c.(7966-7968)atC>atA p.I2656I PAAD 15 51763499 51763499 + Missense_Mutation SNP G G T TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr15:51763499G>T c.7310C>A c.(7309-7311)cCg>cAg p.P2437Q PAAD 15 51772810 51772810 + Missense_Mutation SNP G G A TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr15:51772810G>A c.6493C>T c.(6493-6495)Cat>Tat p.H2165Y PAAD 15 51772901 51772901 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:51772901C>T c.6402G>A c.(6400-6402)ttG>ttA p.L2134L PAAD 15 51780219 51780219 + Nonsense_Mutation SNP C C A TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr15:51780219C>A c.5149G>T c.(5149-5151)Gga>Tga p.G1717* PAAD 15 51791633 51791633 + Missense_Mutation SNP C C T TCGA-F2-A7TX-01A-33D-A38G-08 TCGA-F2-A7TX-10B-01D-A38J-08 g.chr15:51791633C>T c.3788G>A c.(3787-3789)gGa>gAa p.G1263E PAAD 15 51791720 51791720 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:51791720C>T c.3701G>A c.(3700-3702)aGa>aAa p.R1234K PAAD 15 51860756 51860756 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:51860756C>A c.e3-1 PRAD 15 51750826 51750826 + Splice_Site SNP T T C TCGA-EJ-5518-01A-01D-1576-08 TCGA-EJ-5518-10A-01D-1577-08 g.chr15:51750826T>C c.e35-2 PRAD 15 51795002 51795002 + Splice_Site SNP C C T TCGA-G9-6378-01A-11D-1786-08 TCGA-G9-6378-10A-01D-1786-08 g.chr15:51795002C>T c.e17+1 PRAD 15 51795013 51795013 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:51795013C>T c.2982G>A c.(2980-2982)acG>acA p.T994T PRAD 15 51855614 51855614 + Nonsense_Mutation SNP C C T TCGA-EJ-5532-01A-01D-1576-08 TCGA-EJ-5532-10A-01D-1577-08 g.chr15:51855614C>T c.531G>A c.(529-531)tgG>tgA p.W177* READ 15 51791231 51791231 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51791231C>T c.4190G>A c.(4189-4191)cGa>cAa p.R1397Q READ 15 51795011 51795011 + Missense_Mutation SNP G G T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr15:51795011G>T c.2984C>A c.(2983-2985)cCt>cAt p.P995H READ 15 51806663 51806663 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51806663C>A c.2620G>T c.(2620-2622)Gaa>Taa p.E874* READ 15 51828668 51828668 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:51828668T>G c.2009A>C c.(2008-2010)cAt>cCt p.H670P READ 15 51829848 51829848 + Missense_Mutation SNP G G T TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr15:51829848G>T c.1454C>A c.(1453-1455)cCa>cAa p.P485Q READ 15 51839564 51839564 + Nonsense_Mutation SNP C C T TCGA-AG-3878-01A-02W-0899-10 TCGA-AG-3878-10A-01W-0901-10 g.chr15:51839564C>T c.609G>A c.(607-609)tgG>tgA p.W203* SARC 15 51773074 51773074 + Missense_Mutation SNP G G A TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr15:51773074G>A c.6229C>T c.(6229-6231)Ctt>Ttt p.L2077F SARC 15 51791871 51791871 + Missense_Mutation SNP T T A TCGA-DX-AB2P-01A-11D-A387-09 TCGA-DX-AB2P-10A-01D-A38A-09 g.chr15:51791871T>A c.3550A>T c.(3550-3552)Aca>Tca p.T1184S SARC 15 51828631 51828631 + Silent SNP C C T TCGA-MB-A5YA-01A-11D-A29N-09 TCGA-MB-A5YA-10A-01D-A29N-09 g.chr15:51828631C>T c.2046G>A c.(2044-2046)caG>caA p.Q682Q SARC 15 51828727 51828727 + Silent SNP T T C TCGA-QQ-A5VA-01A-12D-A32I-09 TCGA-QQ-A5VA-11A-11D-A32I-09 g.chr15:51828727T>C c.1950A>G c.(1948-1950)cgA>cgG p.R650R SKCM 15 51741329 51741329 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr15:51741329G>A c.8963C>T c.(8962-8964)tCc>tTc p.S2988F SKCM 15 51741329 51741329 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:51741329G>A c.8963C>T c.(8962-8964)tCc>tTc p.S2988F SKCM 15 51741366 51741366 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:51741366G>A c.8926C>T c.(8926-8928)Cta>Tta p.L2976L SKCM 15 51742477 51742477 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr15:51742477G>A c.8750C>T c.(8749-8751)tCg>tTg p.S2917L SKCM 15 51742477 51742477 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:51742477G>A c.8750C>T c.(8749-8751)tCg>tTg p.S2917L SKCM 15 51742485 51742485 + Silent SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr15:51742485G>A c.8742C>T c.(8740-8742)ctC>ctT p.L2914L SKCM 15 51749620 51749620 + Nonsense_Mutation SNP G G A TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr15:51749620G>A c.8176C>T c.(8176-8178)Caa>Taa p.Q2726* SKCM 15 51757773 51757773 + Silent SNP C C T TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr15:51757773C>T c.7593G>A c.(7591-7593)ctG>ctA p.L2531L SKCM 15 51757791 51757791 + Silent SNP G G A TCGA-EE-A29H-06A-12D-A197-08 TCGA-EE-A29H-10A-01D-A199-08 g.chr15:51757791G>A c.7575C>T c.(7573-7575)ttC>ttT p.F2525F SKCM 15 51758421 51758421 + Missense_Mutation SNP C C T TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr15:51758421C>T c.7477G>A c.(7477-7479)Gat>Aat p.D2493N SKCM 15 51758498 51758498 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:51758498G>A c.7400C>T c.(7399-7401)cCt>cTt p.P2467L SKCM 15 51758499 51758499 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:51758499G>A c.7399C>T c.(7399-7401)Cct>Tct p.P2467S SKCM 15 51763533 51763533 + Missense_Mutation SNP G G A TCGA-FS-A4FB-06A-11D-A25O-08 TCGA-FS-A4FB-10B-01D-A25O-08 g.chr15:51763533G>A c.7276C>T c.(7276-7278)Cct>Tct p.P2426S SKCM 15 51763564 51763564 + Silent SNP G G A TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr15:51763564G>A c.7245C>T c.(7243-7245)caC>caT p.H2415H SKCM 15 51766543 51766543 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr15:51766543G>A c.7208C>T c.(7207-7209)tCa>tTa p.S2403L SKCM 15 51766660 51766660 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr15:51766660G>A c.7091C>T c.(7090-7092)tCc>tTc p.S2364F SKCM 15 51772772 51772772 + Missense_Mutation SNP C C T TCGA-D3-A2JC-06A-11D-A19A-08 TCGA-D3-A2JC-10A-01D-A19A-08 g.chr15:51772772C>T c.6531G>A c.(6529-6531)atG>atA p.M2177I SKCM 15 51772866 51772866 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:51772866G>A c.6437C>T c.(6436-6438)tCg>tTg p.S2146L SKCM 15 51772994 51772994 + Silent SNP G G A TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr15:51772994G>A c.6309C>T c.(6307-6309)tcC>tcT p.S2103S SKCM 15 51773239 51773239 + Frame_Shift_Del DEL T T - TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr15:51773239delT c.6064delA c.(6064-6066)acafs p.T2022fs SKCM 15 51773525 51773525 + Silent SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr15:51773525G>A c.5778C>T c.(5776-5778)ttC>ttT p.F1926F SKCM 15 51773612 51773612 + Silent SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:51773612G>A c.5691C>T c.(5689-5691)tgC>tgT p.C1897C SKCM 15 51778369 51778369 + Missense_Mutation SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr15:51778369G>A c.5383C>T c.(5383-5385)Cct>Tct p.P1795S SKCM 15 51780227 51780227 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr15:51780227G>A c.5141C>T c.(5140-5142)tCc>tTc p.S1714F SKCM 15 51780227 51780227 + Missense_Mutation SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr15:51780227G>A c.5141C>T c.(5140-5142)tCc>tTc p.S1714F SKCM 15 51783792 51783792 + Silent SNP G G T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr15:51783792G>T c.4936C>A c.(4936-4938)Cga>Aga p.R1646R SKCM 15 51790822 51790822 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr15:51790822G>A c.4599C>T c.(4597-4599)ttC>ttT p.F1533F SKCM 15 51790919 51790919 + Missense_Mutation SNP T T C TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr15:51790919T>C c.4502A>G c.(4501-4503)tAt>tGt p.Y1501C SKCM 15 51791010 51791010 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:51791010G>A c.4411C>T c.(4411-4413)Ctg>Ttg p.L1471L SKCM 15 51791142 51791142 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr15:51791142G>A c.4279C>T c.(4279-4281)Cct>Tct p.P1427S SKCM 15 51791231 51791231 + Missense_Mutation SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:51791231C>T c.4190G>A c.(4189-4191)cGa>cAa p.R1397Q SKCM 15 51791313 51791313 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:51791313G>A c.4108C>T c.(4108-4110)Cat>Tat p.H1370Y SKCM 15 51791364 51791364 + Silent SNP A A G TCGA-EE-A2GH-06A-11D-A196-08 TCGA-EE-A2GH-10A-01D-A198-08 g.chr15:51791364A>G c.4057T>C c.(4057-4059)Tta>Cta p.L1353L SKCM 15 51791468 51791468 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:51791468G>A c.3953C>T c.(3952-3954)tCt>tTt p.S1318F SKCM 15 51791510 51791510 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:51791510T>G c.3911A>C c.(3910-3912)aAt>aCt p.N1304T SKCM 15 51792133 51792133 + Silent SNP A A T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:51792133A>T c.3288T>A c.(3286-3288)gtT>gtA p.V1096V SKCM 15 51792266 51792266 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:51792266G>A c.3155C>T c.(3154-3156)cCt>cTt p.P1052L SKCM 15 51795147 51795147 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr15:51795147G>A c.2848C>T c.(2848-2850)Cct>Tct p.P950S SKCM 15 51795149 51795149 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:51795149G>A c.2846C>T c.(2845-2847)tCt>tTt p.S949F SKCM 15 51795182 51795182 + Missense_Mutation SNP C C A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr15:51795182C>A c.2813G>T c.(2812-2814)gGa>gTa p.G938V SKCM 15 51795209 51795209 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:51795209G>A c.2786C>T c.(2785-2787)tCc>tTc p.S929F SKCM 15 51828531 51828531 + Missense_Mutation SNP G G A TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr15:51828531G>A c.2146C>T c.(2146-2148)Cat>Tat p.H716Y SKCM 15 51828912 51828912 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:51828912G>A c.1765C>T c.(1765-1767)Cct>Tct p.P589S SKCM 15 51829948 51829948 + Silent SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr15:51829948G>A c.1354C>T c.(1354-1356)Ctg>Ttg p.L452L SKCM 15 51829950 51829950 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr15:51829950G>A c.1352C>T c.(1351-1353)tCc>tTc p.S451F SKCM 15 51830432 51830432 + Silent SNP A A G TCGA-EE-A17Y-06A-11D-A196-08 TCGA-EE-A17Y-10B-01D-A198-08 g.chr15:51830432A>G c.1323T>C c.(1321-1323)ggT>ggC p.G441G SKCM 15 51830440 51830440 + Nonsense_Mutation SNP C C A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr15:51830440C>A c.1315G>T c.(1315-1317)Gaa>Taa p.E439* SKCM 15 51834628 51834628 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:51834628G>A c.1007C>T c.(1006-1008)cCc>cTc p.P336L SKCM 15 51837933 51837933 + Silent SNP T T A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr15:51837933T>A c.777A>T c.(775-777)tcA>tcT p.S259S SKCM 15 51839457 51839457 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr15:51839457G>A c.716C>T c.(715-717)tCg>tTg p.S239L SKCM 15 51839476 51839476 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:51839476G>A c.697C>T c.(697-699)Cga>Tga p.R233* SKCM 15 51839578 51839578 + Missense_Mutation SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr15:51839578G>A c.595C>T c.(595-597)Cct>Tct p.P199S SKCM 15 51857296 51857296 + Nonsense_Mutation SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr15:51857296C>T c.353G>A c.(352-354)tGg>tAg p.W118*

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 15 51772336 51772336 single base substitution C T missense_variant E1553K 4657G>A BLCA-CN 15 51772336 51772336 single base substitution C T missense_variant E2189K 6565G>A BLCA-CN 15 51772336 51772336 single base substitution C T missense_variant E313K 937G>A BLCA-CN 15 51787328 51787328 single base substitution C T missense_variant R1559K 4676G>A BLCA-CN 15 51787328 51787328 single base substitution C T missense_variant R923K 2768G>A BLCA-CN 15 51791561 51791561 single base substitution C A intron_variant BLCA-CN 15 51791561 51791561 single base substitution C A missense_variant S1287I 3860G>T BLCA-US 15 51741202 51741202 single base substitution G T downstream_gene_variant BLCA-US 15 51741202 51741202 single base substitution G T exon_variant BLCA-US 15 51741202 51741202 single base substitution G T missense_variant N1176K 3528C>A BLCA-US 15 51741202 51741202 single base substitution G T missense_variant N2394K 7182C>A BLCA-US 15 51741202 51741202 single base substitution G T missense_variant N3030K 9090C>A BLCA-US 15 51741202 51741202 single base substitution G T missense_variant N3031K 9093C>A BLCA-US 15 51758463 51758463 single base substitution C T exon_variant BLCA-US 15 51758463 51758463 single base substitution C T missense_variant E1843K 5527G>A BLCA-US 15 51758463 51758463 single base substitution C T missense_variant E2479K 7435G>A BLCA-US 15 51758463 51758463 single base substitution C T missense_variant E2480K 7438G>A BLCA-US 15 51758463 51758463 single base substitution C T missense_variant E604K 1810G>A BLCA-US 15 51758502 51758502 single base substitution G C exon_variant BLCA-US 15 51758502 51758502 single base substitution G C missense_variant L1830V 5488C>G BLCA-US 15 51758502 51758502 single base substitution G C missense_variant L2466V 7396C>G BLCA-US 15 51758502 51758502 single base substitution G C missense_variant L2467V 7399C>G BLCA-US 15 51758502 51758502 single base substitution G C missense_variant L591V 1771C>G BLCA-US 15 51772766 51772766 single base substitution G C synonymous_variant L1543L 4629C>G BLCA-US 15 51772766 51772766 single base substitution G C synonymous_variant L2179L 6537C>G BLCA-US 15 51772766 51772766 single base substitution G C synonymous_variant L303L 909C>G BLCA-US 15 51772908 51772908 single base substitution C G missense_variant R1496T 4487G>C BLCA-US 15 51772908 51772908 single base substitution C G missense_variant R2132T 6395G>C BLCA-US 15 51772908 51772908 single base substitution C G missense_variant R256T 767G>C BLCA-US 15 51772963 51772963 single base substitution C T missense_variant E1478K 4432G>A BLCA-US 15 51772963 51772963 single base substitution C T missense_variant E2114K 6340G>A BLCA-US 15 51772963 51772963 single base substitution C T missense_variant E238K 712G>A BLCA-US 15 51772972 51772972 single base substitution C G missense_variant D1475H 4423G>C BLCA-US 15 51772972 51772972 single base substitution C G missense_variant D2111H 6331G>C BLCA-US 15 51772972 51772972 single base substitution C G missense_variant D235H 703G>C BLCA-US 15 51773374 51773374 single base substitution C G missense_variant D101H 301G>C BLCA-US 15 51773374 51773374 single base substitution C G missense_variant D1341H 4021G>C BLCA-US 15 51773374 51773374 single base substitution C G missense_variant D1977H 5929G>C BLCA-US 15 51773566 51773566 single base substitution T C missense_variant K1277E 3829A>G BLCA-US 15 51773566 51773566 single base substitution T C missense_variant K1913E 5737A>G BLCA-US 15 51773566 51773566 single base substitution T C missense_variant K37E 109A>G BLCA-US 15 51778370 51778370 deletion of <=200bp A - frameshift_variant D1158 BLCA-US 15 51778370 51778370 deletion of <=200bp A - frameshift_variant D1794 BLCA-US 15 51778370 51778370 deletion of <=200bp A - upstream_gene_variant BLCA-US 15 51783938 51783938 single base substitution G C missense_variant S1597C 4790C>G BLCA-US 15 51783938 51783938 single base substitution G C missense_variant S961C 2882C>G BLCA-US 15 51791720 51791720 single base substitution C G intron_variant BLCA-US 15 51791720 51791720 single base substitution C G missense_variant R1234T 3701G>C BLCA-US 15 51791720 51791720 single base substitution C T intron_variant BLCA-US 15 51791720 51791720 single base substitution C T missense_variant R1234K 3701G>A BLCA-US 15 51792343 51792343 single base substitution G C intron_variant BLCA-US 15 51792343 51792343 single base substitution G C missense_variant F1026L 3078C>G BLCA-US 15 51795035 51795035 single base substitution G A intron_variant BLCA-US 15 51795035 51795035 single base substitution G A missense_variant S987L 2960C>T BOCA-FR 15 51758851 51758851 single base substitution T C intron_variant BOCA-FR 15 51878129 51878129 single base substitution C T intron_variant BOCA-FR 15 51910908 51910908 single base substitution C T intron_variant BRCA-EU 15 51735138 51735138 single base substitution G A downstream_gene_variant BRCA-EU 15 51735167 51735167 single base substitution C T downstream_gene_variant BRCA-EU 15 51735925 51735925 single base substitution A G downstream_gene_variant BRCA-EU 15 51736287 51736287 single base substitution C G downstream_gene_variant BRCA-EU 15 51737172 51737172 single base substitution C G downstream_gene_variant BRCA-EU 15 51737378 51737378 single base substitution G A downstream_gene_variant BRCA-EU 15 51737382 51737382 single base substitution C T downstream_gene_variant BRCA-EU 15 51737570 51737570 single base substitution A G downstream_gene_variant BRCA-EU 15 51739631 51739631 single base substitution C G downstream_gene_variant BRCA-EU 15 51742552 51742552 single base substitution G A downstream_gene_variant BRCA-EU 15 51742552 51742552 single base substitution G A exon_variant BRCA-EU 15 51742552 51742552 single base substitution G A intron_variant BRCA-EU 15 51742552 51742552 single base substitution G C downstream_gene_variant BRCA-EU 15 51742552 51742552 single base substitution G C exon_variant BRCA-EU 15 51742552 51742552 single base substitution G C intron_variant BRCA-EU 15 51742770 51742770 single base substitution G C downstream_gene_variant BRCA-EU 15 51742770 51742770 single base substitution G C exon_variant BRCA-EU 15 51742770 51742770 single base substitution G C intron_variant BRCA-EU 15 51743724 51743724 single base substitution C T downstream_gene_variant BRCA-EU 15 51743724 51743724 single base substitution C T intron_variant BRCA-EU 15 51743724 51743724 single base substitution C T upstream_gene_variant BRCA-EU 15 51745759 51745759 single base substitution G A downstream_gene_variant BRCA-EU 15 51745759 51745759 single base substitution G A exon_variant BRCA-EU 15 51745759 51745759 single base substitution G A missense_variant S1019F 3056C>T BRCA-EU 15 51745759 51745759 single base substitution G A missense_variant S2237F 6710C>T BRCA-EU 15 51745759 51745759 single base substitution G A missense_variant S2873F 8618C>T BRCA-EU 15 51745759 51745759 single base substitution G A missense_variant S2874F 8621C>T BRCA-EU 15 51745759 51745759 single base substitution G A missense_variant S48F 143C>T BRCA-EU 15 51745759 51745759 single base substitution G A upstream_gene_variant BRCA-EU 15 51746061 51746061 single base substitution A G downstream_gene_variant BRCA-EU 15 51746061 51746061 single base substitution A G intron_variant BRCA-EU 15 51746061 51746061 single base substitution A G upstream_gene_variant BRCA-EU 15 51746972 51746972 single base substitution G A downstream_gene_variant BRCA-EU 15 51746972 51746972 single base substitution G A intron_variant BRCA-EU 15 51746972 51746972 single base substitution G A upstream_gene_variant BRCA-EU 15 51747602 51747602 single base substitution T A downstream_gene_variant BRCA-EU 15 51747602 51747602 single base substitution T A intron_variant BRCA-EU 15 51747602 51747602 single base substitution T A upstream_gene_variant BRCA-EU 15 51750124 51750124 insertion of <=200bp - A intron_variant BRCA-EU 15 51750124 51750124 insertion of <=200bp - A upstream_gene_variant BRCA-EU 15 51750491 51750491 single base substitution A T downstream_gene_variant BRCA-EU 15 51750491 51750491 single base substitution A T intron_variant BRCA-EU 15 51750491 51750491 single base substitution A T upstream_gene_variant BRCA-EU 15 51753545 51753545 single base substitution G A downstream_gene_variant BRCA-EU 15 51753545 51753545 single base substitution G A intron_variant BRCA-EU 15 51753545 51753545 single base substitution G A upstream_gene_variant BRCA-EU 15 51755688 51755688 single base substitution C T exon_variant BRCA-EU 15 51755688 51755688 single base substitution C T intron_variant BRCA-EU 15 51755688 51755688 single base substitution C T missense_variant R1968Q 5903G>A BRCA-EU 15 51755688 51755688 single base substitution C T missense_variant R2604Q 7811G>A BRCA-EU 15 51755688 51755688 single base substitution C T missense_variant R2605Q 7814G>A BRCA-EU 15 51755688 51755688 single base substitution C T missense_variant R729Q 2186G>A BRCA-EU 15 51755688 51755688 single base substitution C T upstream_gene_variant BRCA-EU 15 51756727 51756727 single base substitution A T intron_variant BRCA-EU 15 51756727 51756727 single base substitution A T upstream_gene_variant BRCA-EU 15 51756839 51756839 single base substitution C T intron_variant BRCA-EU 15 51756839 51756839 single base substitution C T upstream_gene_variant BRCA-EU 15 51757578 51757578 single base substitution C T intron_variant BRCA-EU 15 51757849 51757849 single base substitution C T splice_acceptor_variant BRCA-EU 15 51759976 51759976 single base substitution C A intron_variant BRCA-EU 15 51761546 51761546 single base substitution T A intron_variant BRCA-EU 15 51762505 51762505 insertion of <=200bp - T intron_variant BRCA-EU 15 51762956 51762956 single base substitution C A intron_variant BRCA-EU 15 51764766 51764766 single base substitution C G intron_variant BRCA-EU 15 51764766 51764766 single base substitution C G upstream_gene_variant BRCA-EU 15 51767473 51767473 single base substitution G A intron_variant BRCA-EU 15 51767473 51767473 single base substitution G A upstream_gene_variant BRCA-EU 15 51769666 51769666 single base substitution C A intron_variant BRCA-EU 15 51771112 51771112 single base substitution A G intron_variant BRCA-EU 15 51771803 51771803 single base substitution T G intron_variant BRCA-EU 15 51772539 51772539 single base substitution C G intron_variant BRCA-EU 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K1285K? BRCA-EU 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K1921K? BRCA-EU 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K45K? BRCA-EU 15 51777753 51777753 single base substitution G C intron_variant BRCA-EU 15 51777753 51777753 single base substitution G C upstream_gene_variant BRCA-EU 15 51777755 51777755 single base substitution A T intron_variant BRCA-EU 15 51777755 51777755 single base substitution A T upstream_gene_variant BRCA-EU 15 51779152 51779152 deletion of <=200bp A - intron_variant BRCA-EU 15 51781894 51781894 single base substitution A T intron_variant BRCA-EU 15 51782738 51782738 single base substitution G C intron_variant BRCA-EU 15 51785086 51785086 single base substitution A C intron_variant BRCA-EU 15 51786063 51786063 single base substitution G T intron_variant BRCA-EU 15 51791169 51791169 single base substitution G A intron_variant BRCA-EU 15 51791169 51791169 single base substitution G A stop_gained R1418* 4252C>T BRCA-EU 15 51792362 51792362 single base substitution G C intron_variant BRCA-EU 15 51792362 51792362 single base substitution G C missense_variant S1020C 3059C>G BRCA-EU 15 51794618 51794618 single base substitution C G intron_variant BRCA-EU 15 51794875 51794875 single base substitution G C intron_variant BRCA-EU 15 51794980 51794980 single base substitution G C intron_variant BRCA-EU 15 51795990 51795990 single base substitution C T intron_variant BRCA-EU 15 51796010 51796010 single base substitution C A intron_variant BRCA-EU 15 51796237 51796237 single base substitution G A intron_variant BRCA-EU 15 51797558 51797558 single base substitution T C intron_variant BRCA-EU 15 51797685 51797685 single base substitution G C intron_variant BRCA-EU 15 51799727 51799727 single base substitution C A intron_variant BRCA-EU 15 51801057 51801057 single base substitution A G intron_variant BRCA-EU 15 51802035 51802035 single base substitution C T intron_variant BRCA-EU 15 51802619 51802619 single base substitution G A intron_variant BRCA-EU 15 51802682 51802682 single base substitution A C intron_variant BRCA-EU 15 51803552 51803552 single base substitution T C intron_variant BRCA-EU 15 51804486 51804486 single base substitution G A intron_variant BRCA-EU 15 51805346 51805346 single base substitution G A intron_variant BRCA-EU 15 51807840 51807840 single base substitution T A intron_variant BRCA-EU 15 51807962 51807963 deletion of <=200bp TG - intron_variant BRCA-EU 15 51810142 51810142 deletion of <=200bp A - intron_variant BRCA-EU 15 51810266 51810266 single base substitution C T intron_variant BRCA-EU 15 51810320 51810320 single base substitution G T intron_variant BRCA-EU 15 51810718 51810718 single base substitution C G intron_variant BRCA-EU 15 51811147 51811147 single base substitution A G intron_variant BRCA-EU 15 51811489 51811489 deletion of <=200bp T - intron_variant BRCA-EU 15 51811583 51811583 single base substitution G T intron_variant BRCA-EU 15 51814080 51814080 single base substitution G C intron_variant BRCA-EU 15 51816013 51816013 single base substitution C T intron_variant BRCA-EU 15 51816391 51816391 single base substitution C G intron_variant BRCA-EU 15 51816472 51816472 single base substitution G C intron_variant BRCA-EU 15 51817316 51817316 single base substitution C T intron_variant BRCA-EU 15 51817541 51817541 single base substitution T G intron_variant BRCA-EU 15 51817677 51817677 single base substitution C A intron_variant BRCA-EU 15 51817763 51817763 single base substitution C A intron_variant BRCA-EU 15 51818253 51818253 single base substitution G A intron_variant BRCA-EU 15 51820774 51820774 single base substitution C A intron_variant BRCA-EU 15 51821036 51821036 single base substitution G A intron_variant BRCA-EU 15 51821697 51821697 single base substitution C G intron_variant BRCA-EU 15 51821722 51821722 single base substitution A G intron_variant BRCA-EU 15 51823086 51823086 insertion of <=200bp - A intron_variant BRCA-EU 15 51823891 51823891 single base substitution A C intron_variant BRCA-EU 15 51824853 51824853 single base substitution C G intron_variant BRCA-EU 15 51825132 51825132 single base substitution C T intron_variant BRCA-EU 15 51827068 51827068 insertion of <=200bp - TC intron_variant BRCA-EU 15 51828184 51828184 single base substitution C G intron_variant BRCA-EU 15 51828519 51828519 single base substitution C T missense_variant A720T 2158G>A BRCA-EU 15 51829891 51829891 single base substitution C G missense_variant E471Q 1411G>C BRCA-EU 15 51830321 51830321 single base substitution G C intron_variant BRCA-EU 15 51831074 51831074 single base substitution G T intron_variant BRCA-EU 15 51833005 51833005 single base substitution G A intron_variant BRCA-EU 15 51834826 51834826 single base substitution G C downstream_gene_variant BRCA-EU 15 51834826 51834826 single base substitution G C intron_variant BRCA-EU 15 51835420 51835420 single base substitution T G downstream_gene_variant BRCA-EU 15 51835420 51835420 single base substitution T G intron_variant BRCA-EU 15 51836372 51836372 single base substitution G A downstream_gene_variant BRCA-EU 15 51836372 51836372 single base substitution G A intron_variant BRCA-EU 15 51837914 51837914 single base substitution G A downstream_gene_variant BRCA-EU 15 51837914 51837914 single base substitution G A missense_variant R266W 796C>T BRCA-EU 15 51838931 51838931 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 51838931 51838931 deletion of <=200bp A - intron_variant BRCA-EU 15 51839004 51839004 single base substitution C T downstream_gene_variant BRCA-EU 15 51839004 51839004 single base substitution C T intron_variant BRCA-EU 15 51841010 51841010 single base substitution A C intron_variant BRCA-EU 15 51841020 51841020 single base substitution T A intron_variant BRCA-EU 15 51841157 51841157 single base substitution T A intron_variant BRCA-EU 15 51842066 51842066 single base substitution C T intron_variant BRCA-EU 15 51842201 51842201 single base substitution G A intron_variant BRCA-EU 15 51842811 51842811 single base substitution T A intron_variant BRCA-EU 15 51842823 51842823 single base substitution C G intron_variant BRCA-EU 15 51843631 51843631 insertion of <=200bp - G intron_variant BRCA-EU 15 51845674 51845674 deletion of <=200bp A - intron_variant BRCA-EU 15 51846204 51846204 single base substitution C T intron_variant BRCA-EU 15 51846677 51846677 single base substitution C G intron_variant BRCA-EU 15 51847800 51847800 single base substitution A G intron_variant BRCA-EU 15 51847871 51847871 single base substitution T C intron_variant BRCA-EU 15 51848674 51848674 single base substitution A C intron_variant BRCA-EU 15 51850189 51850189 single base substitution A T intron_variant BRCA-EU 15 51851750 51851750 deletion of <=200bp A - intron_variant BRCA-EU 15 51852626 51852626 single base substitution T A intron_variant BRCA-EU 15 51854426 51854426 insertion of <=200bp - AT downstream_gene_variant BRCA-EU 15 51854426 51854426 insertion of <=200bp - AT intron_variant BRCA-EU 15 51855688 51855688 single base substitution T A downstream_gene_variant BRCA-EU 15 51855688 51855688 single base substitution T A intron_variant BRCA-EU 15 51858207 51858207 single base substitution C A downstream_gene_variant BRCA-EU 15 51858207 51858207 single base substitution C A intron_variant BRCA-EU 15 51861081 51861081 single base substitution T A intron_variant BRCA-EU 15 51861241 51861241 single base substitution G C intron_variant BRCA-EU 15 51862736 51862736 single base substitution G C intron_variant BRCA-EU 15 51863207 51863207 single base substitution G A intron_variant BRCA-EU 15 51863816 51863816 single base substitution G A intron_variant BRCA-EU 15 51864155 51864155 single base substitution G T intron_variant BRCA-EU 15 51864704 51864704 single base substitution G A intron_variant BRCA-EU 15 51865567 51865567 single base substitution C T intron_variant BRCA-EU 15 51865736 51865736 single base substitution C A intron_variant BRCA-EU 15 51867549 51867549 single base substitution A G intron_variant BRCA-EU 15 51867709 51867709 single base substitution G A intron_variant BRCA-EU 15 51868570 51868570 single base substitution C T intron_variant BRCA-EU 15 51869250 51869250 single base substitution G C intron_variant BRCA-EU 15 51869811 51869811 single base substitution A C intron_variant BRCA-EU 15 51871434 51871434 single base substitution C T intron_variant BRCA-EU 15 51871785 51871785 single base substitution A C intron_variant BRCA-EU 15 51871860 51871860 single base substitution G C intron_variant BRCA-EU 15 51874083 51874083 deletion of <=200bp A - intron_variant BRCA-EU 15 51878188 51878188 single base substitution G A intron_variant BRCA-EU 15 51878644 51878644 single base substitution G T intron_variant BRCA-EU 15 51885228 51885228 single base substitution A T intron_variant BRCA-EU 15 51885889 51885889 single base substitution G C intron_variant BRCA-EU 15 51886737 51886737 single base substitution G A intron_variant BRCA-EU 15 51887081 51887081 single base substitution C T intron_variant BRCA-EU 15 51887791 51887791 single base substitution C A intron_variant BRCA-EU 15 51888400 51888400 single base substitution T C intron_variant BRCA-EU 15 51888834 51888834 single base substitution C T intron_variant BRCA-EU 15 51889044 51889044 single base substitution C T intron_variant BRCA-EU 15 51889972 51889972 single base substitution A G intron_variant BRCA-EU 15 51890332 51890332 single base substitution A G intron_variant BRCA-EU 15 51890447 51890447 single base substitution T C intron_variant BRCA-EU 15 51892393 51892393 single base substitution G A intron_variant BRCA-EU 15 51892811 51892811 single base substitution G A intron_variant BRCA-EU 15 51893531 51893531 single base substitution A G intron_variant BRCA-EU 15 51895113 51895113 single base substitution T C intron_variant BRCA-EU 15 51895690 51895690 single base substitution G A intron_variant BRCA-EU 15 51896041 51896041 single base substitution G A intron_variant BRCA-EU 15 51896041 51896041 single base substitution G A upstream_gene_variant BRCA-EU 15 51896287 51896287 single base substitution G C intron_variant BRCA-EU 15 51896287 51896287 single base substitution G C upstream_gene_variant BRCA-EU 15 51896821 51896821 deletion of <=200bp T - intron_variant BRCA-EU 15 51896821 51896821 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 51897000 51897000 single base substitution G A intron_variant BRCA-EU 15 51897000 51897000 single base substitution G A upstream_gene_variant BRCA-EU 15 51897409 51897409 deletion of <=200bp T - intron_variant BRCA-EU 15 51897409 51897409 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 51897452 51897452 single base substitution C T intron_variant BRCA-EU 15 51897452 51897452 single base substitution C T upstream_gene_variant BRCA-EU 15 51899256 51899256 single base substitution G A intron_variant BRCA-EU 15 51899256 51899256 single base substitution G A upstream_gene_variant BRCA-EU 15 51899631 51899631 single base substitution C T intron_variant BRCA-EU 15 51899631 51899631 single base substitution C T upstream_gene_variant BRCA-EU 15 51899668 51899668 insertion of <=200bp - A intron_variant BRCA-EU 15 51899668 51899668 insertion of <=200bp - A upstream_gene_variant BRCA-EU 15 51899943 51899943 single base substitution A G intron_variant BRCA-EU 15 51899943 51899943 single base substitution A G upstream_gene_variant BRCA-EU 15 51903403 51903403 single base substitution A T intron_variant BRCA-EU 15 51903513 51903513 single base substitution C T intron_variant BRCA-EU 15 51904530 51904530 single base substitution G A intron_variant BRCA-EU 15 51905365 51905365 single base substitution G A intron_variant BRCA-EU 15 51906564 51906564 single base substitution G C intron_variant BRCA-EU 15 51906730 51906730 single base substitution T C intron_variant BRCA-EU 15 51907911 51907911 single base substitution T C intron_variant BRCA-EU 15 51911306 51911306 single base substitution G C intron_variant BRCA-EU 15 51911390 51911390 single base substitution G A intron_variant BRCA-EU 15 51911987 51911987 single base substitution C G intron_variant BRCA-EU 15 51912483 51912483 single base substitution G C intron_variant BRCA-EU 15 51912835 51912835 single base substitution G C intron_variant BRCA-EU 15 51912849 51912849 single base substitution G A intron_variant BRCA-EU 15 51914267 51914267 single base substitution A C intron_variant BRCA-EU 15 51914545 51914545 single base substitution G A intron_variant BRCA-EU 15 51918490 51918490 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 51918621 51918621 single base substitution A G upstream_gene_variant BRCA-EU 15 51919923 51919923 single base substitution T C upstream_gene_variant BRCA-FR 15 51745759 51745759 single base substitution G A downstream_gene_variant BRCA-FR 15 51745759 51745759 single base substitution G A exon_variant BRCA-FR 15 51745759 51745759 single base substitution G A missense_variant S1019F 3056C>T BRCA-FR 15 51745759 51745759 single base substitution G A missense_variant S2237F 6710C>T BRCA-FR 15 51745759 51745759 single base substitution G A missense_variant S2873F 8618C>T BRCA-FR 15 51745759 51745759 single base substitution G A missense_variant S2874F 8621C>T BRCA-FR 15 51745759 51745759 single base substitution G A missense_variant S48F 143C>T BRCA-FR 15 51745759 51745759 single base substitution G A upstream_gene_variant BRCA-FR 15 51746972 51746972 single base substitution G A downstream_gene_variant BRCA-FR 15 51746972 51746972 single base substitution G A intron_variant BRCA-FR 15 51746972 51746972 single base substitution G A upstream_gene_variant BRCA-FR 15 51750491 51750491 single base substitution A T downstream_gene_variant BRCA-FR 15 51750491 51750491 single base substitution A T intron_variant BRCA-FR 15 51750491 51750491 single base substitution A T upstream_gene_variant BRCA-FR 15 51755688 51755688 single base substitution C T exon_variant BRCA-FR 15 51755688 51755688 single base substitution C T intron_variant BRCA-FR 15 51755688 51755688 single base substitution C T missense_variant R1968Q 5903G>A BRCA-FR 15 51755688 51755688 single base substitution C T missense_variant R2604Q 7811G>A BRCA-FR 15 51755688 51755688 single base substitution C T missense_variant R2605Q 7814G>A BRCA-FR 15 51755688 51755688 single base substitution C T missense_variant R729Q 2186G>A BRCA-FR 15 51755688 51755688 single base substitution C T upstream_gene_variant BRCA-FR 15 51757551 51757551 single base substitution C T intron_variant BRCA-FR 15 51764766 51764766 single base substitution C G intron_variant BRCA-FR 15 51764766 51764766 single base substitution C G upstream_gene_variant BRCA-FR 15 51769666 51769666 single base substitution C A intron_variant BRCA-FR 15 51775501 51775501 single base substitution C T intron_variant BRCA-FR 15 51775501 51775501 single base substitution C T upstream_gene_variant BRCA-FR 15 51790338 51790338 single base substitution G A intron_variant BRCA-FR 15 51791169 51791169 single base substitution G A intron_variant BRCA-FR 15 51791169 51791169 single base substitution G A stop_gained R1418* 4252C>T BRCA-FR 15 51794875 51794875 single base substitution G C intron_variant BRCA-FR 15 51797685 51797685 single base substitution G C intron_variant BRCA-FR 15 51806351 51806351 single base substitution T C intron_variant BRCA-FR 15 51814080 51814080 single base substitution G C intron_variant BRCA-FR 15 51816391 51816391 single base substitution C G intron_variant BRCA-FR 15 51839004 51839004 single base substitution C T downstream_gene_variant BRCA-FR 15 51839004 51839004 single base substitution C T intron_variant BRCA-FR 15 51841020 51841020 single base substitution T A intron_variant BRCA-FR 15 51841324 51841324 single base substitution C T intron_variant BRCA-FR 15 51842823 51842823 single base substitution C G intron_variant BRCA-FR 15 51843460 51843460 single base substitution G A intron_variant BRCA-FR 15 51846677 51846677 single base substitution C G intron_variant BRCA-FR 15 51847800 51847800 single base substitution A G intron_variant BRCA-FR 15 51859845 51859845 single base substitution G A exon_variant BRCA-FR 15 51859845 51859845 single base substitution G A intron_variant BRCA-FR 15 51861241 51861241 single base substitution G C intron_variant BRCA-FR 15 51863816 51863816 single base substitution G A intron_variant BRCA-FR 15 51864155 51864155 single base substitution G T intron_variant BRCA-FR 15 51884139 51884139 single base substitution T C intron_variant BRCA-FR 15 51890332 51890332 single base substitution A G intron_variant BRCA-FR 15 51892653 51892653 single base substitution A G intron_variant BRCA-FR 15 51893505 51893505 single base substitution T A intron_variant BRCA-FR 15 51906564 51906564 single base substitution G C intron_variant BRCA-FR 15 51911306 51911306 single base substitution G C intron_variant BRCA-FR 15 51911390 51911390 single base substitution G A intron_variant BRCA-FR 15 51912483 51912483 single base substitution G C intron_variant BRCA-FR 15 51919835 51919835 single base substitution G A upstream_gene_variant BRCA-UK 15 51749407 51749407 single base substitution C T downstream_gene_variant BRCA-UK 15 51749407 51749407 single base substitution C T intron_variant BRCA-UK 15 51749407 51749407 single base substitution C T upstream_gene_variant BRCA-UK 15 51756727 51756727 single base substitution A T intron_variant BRCA-UK 15 51756727 51756727 single base substitution A T upstream_gene_variant BRCA-UK 15 51757849 51757849 single base substitution C T splice_acceptor_variant BRCA-UK 15 51758156 51758156 single base substitution C T intron_variant BRCA-UK 15 51770217 51770217 single base substitution C G intron_variant BRCA-UK 15 51780241 51780241 single base substitution C G missense_variant L1073F 3219G>C BRCA-UK 15 51780241 51780241 single base substitution C G missense_variant L1709F 5127G>C BRCA-UK 15 51802619 51802619 single base substitution G A intron_variant BRCA-UK 15 51805217 51805217 single base substitution G C intron_variant BRCA-UK 15 51810474 51810474 single base substitution G A intron_variant BRCA-UK 15 51818253 51818253 single base substitution G A intron_variant BRCA-UK 15 51848527 51848527 single base substitution G A intron_variant BRCA-UK 15 51855581 51855581 single base substitution T C downstream_gene_variant BRCA-UK 15 51855581 51855581 single base substitution T C exon_variant BRCA-UK 15 51855581 51855581 single base substitution T C synonymous_variant G188G 564A>G BRCA-UK 15 51869811 51869811 single base substitution A C intron_variant BRCA-US 15 51742471 51742471 single base substitution C T downstream_gene_variant BRCA-US 15 51742471 51742471 single base substitution C T exon_variant BRCA-US 15 51742471 51742471 single base substitution C T missense_variant G1065D 3194G>A BRCA-US 15 51742471 51742471 single base substitution C T missense_variant G2283D 6848G>A BRCA-US 15 51742471 51742471 single base substitution C T missense_variant G2919D 8756G>A BRCA-US 15 51742471 51742471 single base substitution C T missense_variant G2920D 8759G>A BRCA-US 15 51742471 51742471 single base substitution C T synonymous_variant G76G 228G>A BRCA-US 15 51751869 51751869 single base substitution C A downstream_gene_variant BRCA-US 15 51751869 51751869 single base substitution C A exon_variant BRCA-US 15 51751869 51751869 single base substitution C A intron_variant BRCA-US 15 51751869 51751869 single base substitution C A upstream_gene_variant BRCA-US 15 51756941 51756941 single base substitution A T exon_variant BRCA-US 15 51756941 51756941 single base substitution A T intron_variant BRCA-US 15 51756941 51756941 single base substitution A T missense_variant L1943H 5828T>A BRCA-US 15 51756941 51756941 single base substitution A T missense_variant L2579H 7736T>A BRCA-US 15 51756941 51756941 single base substitution A T missense_variant L2580H 7739T>A BRCA-US 15 51756941 51756941 single base substitution A T missense_variant L704H 2111T>A BRCA-US 15 51756941 51756941 single base substitution A T upstream_gene_variant BRCA-US 15 51766573 51766575 deletion of <=200bp ACA - disruptive_inframe_deletion VV1756V BRCA-US 15 51766573 51766575 deletion of <=200bp ACA - disruptive_inframe_deletion VV2392V BRCA-US 15 51766573 51766575 deletion of <=200bp ACA - disruptive_inframe_deletion VV2393V BRCA-US 15 51766573 51766575 deletion of <=200bp ACA - disruptive_inframe_deletion VV517V BRCA-US 15 51766573 51766575 deletion of <=200bp ACA - upstream_gene_variant BRCA-US 15 51766785 51766785 single base substitution C G synonymous_variant V1686V 5058G>C BRCA-US 15 51766785 51766785 single base substitution C G synonymous_variant V2322V 6966G>C BRCA-US 15 51766785 51766785 single base substitution C G synonymous_variant V2323V 6969G>C BRCA-US 15 51766785 51766785 single base substitution C G synonymous_variant V447V 1341G>C BRCA-US 15 51766785 51766785 single base substitution C G upstream_gene_variant BRCA-US 15 51772888 51772888 single base substitution C G missense_variant E1503Q 4507G>C BRCA-US 15 51772888 51772888 single base substitution C G missense_variant E2139Q 6415G>C BRCA-US 15 51772888 51772888 single base substitution C G missense_variant E263Q 787G>C BRCA-US 15 51773047 51773047 single base substitution C T missense_variant E1450K 4348G>A BRCA-US 15 51773047 51773047 single base substitution C T missense_variant E2086K 6256G>A BRCA-US 15 51773047 51773047 single base substitution C T missense_variant E210K 628G>A BRCA-US 15 51773279 51773279 single base substitution T C synonymous_variant K132K 396A>G BRCA-US 15 51773279 51773279 single base substitution T C synonymous_variant K1372K 4116A>G BRCA-US 15 51773279 51773279 single base substitution T C synonymous_variant K2008K 6024A>G BRCA-US 15 51773348 51773348 single base substitution G A synonymous_variant A109A 327C>T BRCA-US 15 51773348 51773348 single base substitution G A synonymous_variant A1349A 4047C>T BRCA-US 15 51773348 51773348 single base substitution G A synonymous_variant A1985A 5955C>T BRCA-US 15 51773769 51773769 single base substitution C T missense_variant R1209Q 3626G>A BRCA-US 15 51773769 51773769 single base substitution C T missense_variant R1845Q 5534G>A BRCA-US 15 51773769 51773769 single base substitution C T upstream_gene_variant BRCA-US 15 51778354 51778354 single base substitution G A missense_variant L1164F 3490C>T BRCA-US 15 51778354 51778354 single base substitution G A missense_variant L1800F 5398C>T BRCA-US 15 51778354 51778354 single base substitution G A upstream_gene_variant BRCA-US 15 51778522 51778522 single base substitution T G missense_variant K1108Q 3322A>C BRCA-US 15 51778522 51778522 single base substitution T G missense_variant K1744Q 5230A>C BRCA-US 15 51778522 51778522 single base substitution T G upstream_gene_variant BRCA-US 15 51778534 51778534 single base substitution C A missense_variant V1104L 3310G>T BRCA-US 15 51778534 51778534 single base substitution C A missense_variant V1740L 5218G>T BRCA-US 15 51778534 51778534 single base substitution C A upstream_gene_variant BRCA-US 15 51780803 51780803 single base substitution C G missense_variant D1029H 3085G>C BRCA-US 15 51780803 51780803 single base substitution C G missense_variant D1665H 4993G>C BRCA-US 15 51780830 51780830 deletion of <=200bp A - frameshift_variant S1020 BRCA-US 15 51780830 51780830 deletion of <=200bp A - frameshift_variant S1656 BRCA-US 15 51783884 51783884 single base substitution T C missense_variant N1615S 4844A>G BRCA-US 15 51783884 51783884 single base substitution T C missense_variant N979S 2936A>G BRCA-US 15 51787275 51787275 single base substitution T C missense_variant T1577A 4729A>G BRCA-US 15 51787275 51787275 single base substitution T C missense_variant T941A 2821A>G BRCA-US 15 51790768 51790768 deletion of <=200bp G - frameshift_variant S1551 BRCA-US 15 51790768 51790768 deletion of <=200bp G - intron_variant BRCA-US 15 51790773 51790774 deletion of <=200bp CA - frameshift_variant DE1549 BRCA-US 15 51790773 51790774 deletion of <=200bp CA - intron_variant BRCA-US 15 51791547 51791547 single base substitution C T intron_variant BRCA-US 15 51791547 51791547 single base substitution C T missense_variant E1292K 3874G>A BRCA-US 15 51792037 51792037 single base substitution C A intron_variant BRCA-US 15 51792037 51792037 single base substitution C A missense_variant L1128F 3384G>T BRCA-US 15 51799419 51799419 single base substitution G T missense_variant F892L 2676C>A BRCA-US 15 51828435 51828435 single base substitution T G missense_variant I748L 2242A>C BRCA-US 15 51828902 51828902 single base substitution G C stop_gained S592* 1775C>G BRCA-US 15 51828921 51828921 single base substitution C G missense_variant V586L 1756G>C BRCA-US 15 51837848 51837848 single base substitution T G downstream_gene_variant BRCA-US 15 51837848 51837848 single base substitution T G missense_variant T288P 862A>C BRCA-US 15 51857358 51857358 single base substitution G C downstream_gene_variant BRCA-US 15 51857358 51857358 single base substitution G C exon_variant BRCA-US 15 51857358 51857358 single base substitution G C synonymous_variant L97L 291C>G BTCA-JP 15 51749411 51749411 single base substitution G A downstream_gene_variant BTCA-JP 15 51749411 51749411 single base substitution G A intron_variant BTCA-JP 15 51749411 51749411 single base substitution G A upstream_gene_variant BTCA-JP 15 51766475 51766475 insertion of <=200bp - A intron_variant BTCA-JP 15 51766475 51766475 insertion of <=200bp - A upstream_gene_variant BTCA-JP 15 51766637 51766637 single base substitution C A missense_variant A1736S 5206G>T BTCA-JP 15 51766637 51766637 single base substitution C A missense_variant A2372S 7114G>T BTCA-JP 15 51766637 51766637 single base substitution C A missense_variant A2373S 7117G>T BTCA-JP 15 51766637 51766637 single base substitution C A missense_variant A497S 1489G>T BTCA-JP 15 51766637 51766637 single base substitution C A upstream_gene_variant BTCA-JP 15 51780056 51780056 single base substitution A G intron_variant BTCA-JP 15 51780838 51780838 single base substitution G A missense_variant A1017V 3050C>T BTCA-JP 15 51780838 51780838 single base substitution G A missense_variant A1653V 4958C>T BTCA-JP 15 51783797 51783797 single base substitution G A missense_variant T1008M 3023C>T BTCA-JP 15 51783797 51783797 single base substitution G A missense_variant T1644M 4931C>T BTCA-JP 15 51791717 51791717 single base substitution G C intron_variant BTCA-JP 15 51791717 51791717 single base substitution G C missense_variant S1235C 3704C>G BTCA-JP 15 51791774 51791774 single base substitution A G intron_variant BTCA-JP 15 51791774 51791774 single base substitution A G missense_variant L1216S 3647T>C BTCA-JP 15 51827922 51827922 single base substitution G A missense_variant L792F 2374C>T BTCA-JP 15 51828933 51828933 single base substitution C G missense_variant E582Q 1744G>C CESC-US 15 51748511 51748511 single base substitution T C downstream_gene_variant CESC-US 15 51748511 51748511 single base substitution T C exon_variant CESC-US 15 51748511 51748511 single base substitution T C missense_variant Q2140R 6419A>G CESC-US 15 51748511 51748511 single base substitution T C missense_variant Q2776R 8327A>G CESC-US 15 51748511 51748511 single base substitution T C missense_variant Q2777R 8330A>G CESC-US 15 51748511 51748511 single base substitution T C missense_variant Q922R 2765A>G CESC-US 15 51748511 51748511 single base substitution T C upstream_gene_variant CESC-US 15 51748512 51748512 single base substitution G C downstream_gene_variant CESC-US 15 51748512 51748512 single base substitution G C exon_variant CESC-US 15 51748512 51748512 single base substitution G C missense_variant Q2140E 6418C>G CESC-US 15 51748512 51748512 single base substitution G C missense_variant Q2776E 8326C>G CESC-US 15 51748512 51748512 single base substitution G C missense_variant Q2777E 8329C>G CESC-US 15 51748512 51748512 single base substitution G C missense_variant Q922E 2764C>G CESC-US 15 51748512 51748512 single base substitution G C upstream_gene_variant CESC-US 15 51755661 51755661 single base substitution C T exon_variant CESC-US 15 51755661 51755661 single base substitution C T intron_variant CESC-US 15 51755661 51755661 single base substitution C T missense_variant R1977Q 5930G>A CESC-US 15 51755661 51755661 single base substitution C T missense_variant R2613Q 7838G>A CESC-US 15 51755661 51755661 single base substitution C T missense_variant R2614Q 7841G>A CESC-US 15 51755661 51755661 single base substitution C T missense_variant R738Q 2213G>A CESC-US 15 51755661 51755661 single base substitution C T upstream_gene_variant CESC-US 15 51768825 51768825 single base substitution C G missense_variant E1672Q 5014G>C CESC-US 15 51768825 51768825 single base substitution C G missense_variant E2308Q 6922G>C CESC-US 15 51768825 51768825 single base substitution C G missense_variant E2309Q 6925G>C CESC-US 15 51768825 51768825 single base substitution C G missense_variant E433Q 1297G>C CESC-US 15 51768828 51768828 single base substitution C T missense_variant E1671K 5011G>A CESC-US 15 51768828 51768828 single base substitution C T missense_variant E2307K 6919G>A CESC-US 15 51768828 51768828 single base substitution C T missense_variant E2308K 6922G>A CESC-US 15 51768828 51768828 single base substitution C T missense_variant E432K 1294G>A CESC-US 15 51773272 51773272 single base substitution C G missense_variant D135H 403G>C CESC-US 15 51773272 51773272 single base substitution C G missense_variant D1375H 4123G>C CESC-US 15 51773272 51773272 single base substitution C G missense_variant D2011H 6031G>C CESC-US 15 51778394 51778394 single base substitution G A synonymous_variant F1150F 3450C>T CESC-US 15 51778394 51778394 single base substitution G A synonymous_variant F1786F 5358C>T CESC-US 15 51778394 51778394 single base substitution G A upstream_gene_variant CESC-US 15 51790822 51790822 single base substitution G A intron_variant CESC-US 15 51790822 51790822 single base substitution G A synonymous_variant F1533F 4599C>T CESC-US 15 51828558 51828558 single base substitution G C missense_variant L707V 2119C>G CESC-US 15 51857317 51857317 single base substitution G A downstream_gene_variant CESC-US 15 51857317 51857317 single base substitution G A exon_variant CESC-US 15 51857317 51857317 single base substitution G A missense_variant S111F 332C>T CESC-US 15 51868299 51868299 single base substitution C G exon_variant CESC-US 15 51868299 51868299 single base substitution C G missense_variant G56A 167G>C CLLE-ES 15 51737050 51737050 single base substitution C T downstream_gene_variant CLLE-ES 15 51737559 51737559 single base substitution C T downstream_gene_variant CLLE-ES 15 51737645 51737645 single base substitution C A downstream_gene_variant CLLE-ES 15 51745273 51745273 single base substitution G A downstream_gene_variant CLLE-ES 15 51745273 51745273 single base substitution G A intron_variant CLLE-ES 15 51745273 51745273 single base substitution G A upstream_gene_variant CLLE-ES 15 51755631 51755631 single base substitution A G exon_variant CLLE-ES 15 51755631 51755631 single base substitution A G intron_variant CLLE-ES 15 51755631 51755631 single base substitution A G missense_variant V1987A 5960T>C CLLE-ES 15 51755631 51755631 single base substitution A G missense_variant V2623A 7868T>C CLLE-ES 15 51755631 51755631 single base substitution A G missense_variant V2624A 7871T>C CLLE-ES 15 51755631 51755631 single base substitution A G missense_variant V748A 2243T>C CLLE-ES 15 51755631 51755631 single base substitution A G upstream_gene_variant CLLE-ES 15 51765062 51765062 single base substitution C A intron_variant CLLE-ES 15 51765062 51765062 single base substitution C A upstream_gene_variant CLLE-ES 15 51773533 51773533 single base substitution G A missense_variant P1288S 3862C>T CLLE-ES 15 51773533 51773533 single base substitution G A missense_variant P1924S 5770C>T CLLE-ES 15 51773533 51773533 single base substitution G A missense_variant P48S 142C>T CLLE-ES 15 51780210 51780210 single base substitution G A missense_variant R1084C 3250C>T CLLE-ES 15 51780210 51780210 single base substitution G A missense_variant R1720C 5158C>T CLLE-ES 15 51788402 51788402 single base substitution G A intron_variant CLLE-ES 15 51796025 51796025 single base substitution A C intron_variant CLLE-ES 15 51800024 51800025 deletion of <=200bp TT - intron_variant CLLE-ES 15 51810276 51810276 single base substitution T A intron_variant CLLE-ES 15 51820881 51820881 single base substitution G A intron_variant CLLE-ES 15 51841829 51841829 single base substitution G T intron_variant CLLE-ES 15 51862803 51862803 single base substitution C T intron_variant CLLE-ES 15 51872149 51872149 single base substitution A G intron_variant CLLE-ES 15 51878053 51878053 single base substitution C T intron_variant COAD-US 15 51749621 51749621 single base substitution A G downstream_gene_variant COAD-US 15 51749621 51749621 single base substitution A G exon_variant COAD-US 15 51749621 51749621 single base substitution A G synonymous_variant Y2089Y 6267T>C COAD-US 15 51749621 51749621 single base substitution A G synonymous_variant Y2725Y 8175T>C COAD-US 15 51749621 51749621 single base substitution A G synonymous_variant Y2726Y 8178T>C COAD-US 15 51749621 51749621 single base substitution A G synonymous_variant Y871Y 2613T>C COAD-US 15 51749621 51749621 single base substitution A G upstream_gene_variant COAD-US 15 51766596 51766596 deletion of <=200bp A - frameshift_variant F1749 COAD-US 15 51766596 51766596 deletion of <=200bp A - frameshift_variant F2385 COAD-US 15 51766596 51766596 deletion of <=200bp A - frameshift_variant F2386 COAD-US 15 51766596 51766596 deletion of <=200bp A - frameshift_variant F510 COAD-US 15 51766596 51766596 deletion of <=200bp A - upstream_gene_variant COAD-US 15 51766772 51766772 single base substitution T G missense_variant N1691H 5071A>C COAD-US 15 51766772 51766772 single base substitution T G missense_variant N2327H 6979A>C COAD-US 15 51766772 51766772 single base substitution T G missense_variant N2328H 6982A>C COAD-US 15 51766772 51766772 single base substitution T G missense_variant N452H 1354A>C COAD-US 15 51766772 51766772 single base substitution T G upstream_gene_variant COAD-US 15 51780207 51780207 single base substitution A G missense_variant F1085L 3253T>C COAD-US 15 51780207 51780207 single base substitution A G missense_variant F1721L 5161T>C COAD-US 15 51780284 51780284 deletion of <=200bp A - frameshift_variant F1059 COAD-US 15 51780284 51780284 deletion of <=200bp A - frameshift_variant F1695 COAD-US 15 51790932 51790932 single base substitution T G intron_variant COAD-US 15 51790932 51790932 single base substitution T G missense_variant N1497H 4489A>C COAD-US 15 51791307 51791307 single base substitution C A intron_variant COAD-US 15 51791307 51791307 single base substitution C A missense_variant V1372L 4114G>T COAD-US 15 51791627 51791627 single base substitution T C intron_variant COAD-US 15 51791627 51791627 single base substitution T C missense_variant D1265G 3794A>G COAD-US 15 51791933 51791933 single base substitution G A intron_variant COAD-US 15 51791933 51791933 single base substitution G A missense_variant P1163L 3488C>T COAD-US 15 51795023 51795023 single base substitution A G intron_variant COAD-US 15 51795023 51795023 single base substitution A G missense_variant I991T 2972T>C COAD-US 15 51795175 51795175 single base substitution C A intron_variant COAD-US 15 51795175 51795175 single base substitution C A missense_variant K940N 2820G>T COAD-US 15 51799364 51799364 single base substitution G A missense_variant H911Y 2731C>T COAD-US 15 51809289 51809289 single base substitution C T missense_variant A838T 2512G>A COAD-US 15 51828437 51828437 single base substitution C T missense_variant R747Q 2240G>A COAD-US 15 51828909 51828909 single base substitution G A missense_variant H590Y 1768C>T COAD-US 15 51829839 51829839 single base substitution G A missense_variant T488M 1463C>T COAD-US 15 51830542 51830542 single base substitution C T missense_variant E405K 1213G>A COAD-US 15 51860704 51860704 single base substitution T G exon_variant COAD-US 15 51860704 51860704 single base substitution T G missense_variant N89H 265A>C COAD-US 15 51868381 51868381 deletion of <=200bp A - splice_region_variant COAD-US 15 51868381 51868384 deletion of <=200bp AAAA - splice_region_variant COCA-CN 15 51742545 51742545 single base substitution T C downstream_gene_variant COCA-CN 15 51742545 51742545 single base substitution T C exon_variant COCA-CN 15 51742545 51742545 single base substitution T C splice_acceptor_variant COCA-CN 15 51747469 51747469 single base substitution A C downstream_gene_variant COCA-CN 15 51747469 51747469 single base substitution A C intron_variant COCA-CN 15 51747469 51747469 single base substitution A C upstream_gene_variant COCA-CN 15 51748575 51748575 single base substitution G A downstream_gene_variant COCA-CN 15 51748575 51748575 single base substitution G A intron_variant COCA-CN 15 51748575 51748575 single base substitution G A upstream_gene_variant COCA-CN 15 51750732 51750732 single base substitution G A 3_prime_UTR_variant COCA-CN 15 51750732 51750732 single base substitution G A downstream_gene_variant COCA-CN 15 51750732 51750732 single base substitution G A exon_variant COCA-CN 15 51750732 51750732 single base substitution G A synonymous_variant I2065I 6195C>T COCA-CN 15 51750732 51750732 single base substitution G A synonymous_variant I2701I 8103C>T COCA-CN 15 51750732 51750732 single base substitution G A synonymous_variant I2702I 8106C>T COCA-CN 15 51750732 51750732 single base substitution G A synonymous_variant I847I 2541C>T COCA-CN 15 51750732 51750732 single base substitution G A upstream_gene_variant COCA-CN 15 51750846 51750846 single base substitution G A downstream_gene_variant COCA-CN 15 51750846 51750846 single base substitution G A exon_variant COCA-CN 15 51750846 51750846 single base substitution G A intron_variant COCA-CN 15 51750846 51750846 single base substitution G A upstream_gene_variant COCA-CN 15 51750958 51750958 single base substitution G A 3_prime_UTR_variant COCA-CN 15 51750958 51750958 single base substitution G A downstream_gene_variant COCA-CN 15 51750958 51750958 single base substitution G A exon_variant COCA-CN 15 51750958 51750958 single base substitution G A missense_variant A2017V 6050C>T COCA-CN 15 51750958 51750958 single base substitution G A missense_variant A2653V 7958C>T COCA-CN 15 51750958 51750958 single base substitution G A missense_variant A2654V 7961C>T COCA-CN 15 51750958 51750958 single base substitution G A missense_variant A799V 2396C>T COCA-CN 15 51750958 51750958 single base substitution G A upstream_gene_variant COCA-CN 15 51751848 51751848 single base substitution C A downstream_gene_variant COCA-CN 15 51751848 51751848 single base substitution C A exon_variant COCA-CN 15 51751848 51751848 single base substitution C A intron_variant COCA-CN 15 51751848 51751848 single base substitution C A stop_gained E770* 2308G>T COCA-CN 15 51751848 51751848 single base substitution C A upstream_gene_variant COCA-CN 15 51766615 51766615 single base substitution C T missense_variant R1743Q 5228G>A COCA-CN 15 51766615 51766615 single base substitution C T missense_variant R2379Q 7136G>A COCA-CN 15 51766615 51766615 single base substitution C T missense_variant R2380Q 7139G>A COCA-CN 15 51766615 51766615 single base substitution C T missense_variant R504Q 1511G>A COCA-CN 15 51766615 51766615 single base substitution C T upstream_gene_variant COCA-CN 15 51768761 51768761 single base substitution T G intron_variant COCA-CN 15 51773664 51773664 single base substitution A G missense_variant I1244T 3731T>C COCA-CN 15 51773664 51773664 single base substitution A G missense_variant I1880T 5639T>C COCA-CN 15 51773664 51773664 single base substitution A G missense_variant I4T 11T>C COCA-CN 15 51783836 51783836 single base substitution C A missense_variant R1631I 4892G>T COCA-CN 15 51783836 51783836 single base substitution C A missense_variant R995I 2984G>T COCA-CN 15 51790707 51790707 single base substitution C A intron_variant COCA-CN 15 51790804 51790804 single base substitution A T intron_variant COCA-CN 15 51790804 51790804 single base substitution A T missense_variant D1539E 4617T>A COCA-CN 15 51791588 51791588 single base substitution A G intron_variant COCA-CN 15 51791588 51791588 single base substitution A G missense_variant V1278A 3833T>C COCA-CN 15 51791613 51791613 single base substitution C A intron_variant COCA-CN 15 51791613 51791613 single base substitution C A missense_variant V1270L 3808G>T COCA-CN 15 51806872 51806872 single base substitution C A intron_variant COCA-CN 15 51809122 51809122 single base substitution T C intron_variant COCA-CN 15 51828498 51828498 single base substitution G T missense_variant L727M 2179C>A COCA-CN 15 51828608 51828608 single base substitution C A missense_variant S690I 2069G>T COCA-CN 15 51830052 51830052 single base substitution C A intron_variant COCA-CN 15 51834574 51834574 single base substitution G A downstream_gene_variant COCA-CN 15 51834574 51834574 single base substitution G A missense_variant A354V 1061C>T COCA-CN 15 51837696 51837696 single base substitution G A downstream_gene_variant COCA-CN 15 51837696 51837696 single base substitution G A intron_variant COCA-CN 15 51838103 51838103 single base substitution C A downstream_gene_variant COCA-CN 15 51838103 51838103 single base substitution C A intron_variant EOPC-DE 15 51750958 51750958 single base substitution G A 3_prime_UTR_variant EOPC-DE 15 51750958 51750958 single base substitution G A downstream_gene_variant EOPC-DE 15 51750958 51750958 single base substitution G A exon_variant EOPC-DE 15 51750958 51750958 single base substitution G A missense_variant A2017V 6050C>T EOPC-DE 15 51750958 51750958 single base substitution G A missense_variant A2653V 7958C>T EOPC-DE 15 51750958 51750958 single base substitution G A missense_variant A2654V 7961C>T EOPC-DE 15 51750958 51750958 single base substitution G A missense_variant A799V 2396C>T EOPC-DE 15 51750958 51750958 single base substitution G A upstream_gene_variant EOPC-DE 15 51753534 51753534 single base substitution C T downstream_gene_variant EOPC-DE 15 51753534 51753534 single base substitution C T intron_variant EOPC-DE 15 51753534 51753534 single base substitution C T upstream_gene_variant EOPC-DE 15 51770544 51770544 single base substitution C A missense_variant V1617L 4849G>T EOPC-DE 15 51770544 51770544 single base substitution C A missense_variant V2253L 6757G>T EOPC-DE 15 51770544 51770544 single base substitution C A missense_variant V377L 1129G>T EOPC-DE 15 51844226 51844226 single base substitution T G intron_variant EOPC-DE 15 51849105 51849105 single base substitution C G intron_variant EOPC-DE 15 51883859 51883859 single base substitution A C intron_variant ESAD-UK 15 51735512 51735512 single base substitution C A downstream_gene_variant ESAD-UK 15 51736441 51736441 single base substitution A G downstream_gene_variant ESAD-UK 15 51738847 51738847 single base substitution G A downstream_gene_variant ESAD-UK 15 51740980 51740980 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 15 51740980 51740980 deletion of <=200bp T - downstream_gene_variant ESAD-UK 15 51740980 51740980 deletion of <=200bp T - exon_variant ESAD-UK 15 51742040 51742040 single base substitution C A downstream_gene_variant ESAD-UK 15 51742040 51742040 single base substitution C A intron_variant ESAD-UK 15 51742319 51742319 single base substitution G A downstream_gene_variant ESAD-UK 15 51742319 51742319 single base substitution G A intron_variant ESAD-UK 15 51742319 51742319 single base substitution G A splice_region_variant ESAD-UK 15 51742497 51742497 single base substitution G C downstream_gene_variant ESAD-UK 15 51742497 51742497 single base substitution G C exon_variant ESAD-UK 15 51742497 51742497 single base substitution G C missense_variant Q68E 202C>G ESAD-UK 15 51742497 51742497 single base substitution G C synonymous_variant P1056P 3168C>G ESAD-UK 15 51742497 51742497 single base substitution G C synonymous_variant P2274P 6822C>G ESAD-UK 15 51742497 51742497 single base substitution G C synonymous_variant P2910P 8730C>G ESAD-UK 15 51742497 51742497 single base substitution G C synonymous_variant P2911P 8733C>G ESAD-UK 15 51743719 51743719 single base substitution T G downstream_gene_variant ESAD-UK 15 51743719 51743719 single base substitution T G intron_variant ESAD-UK 15 51743719 51743719 single base substitution T G upstream_gene_variant ESAD-UK 15 51744403 51744403 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 51744403 51744403 deletion of <=200bp A - intron_variant ESAD-UK 15 51744403 51744403 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 51745355 51745355 single base substitution C T downstream_gene_variant ESAD-UK 15 51745355 51745355 single base substitution C T intron_variant ESAD-UK 15 51745355 51745355 single base substitution C T upstream_gene_variant ESAD-UK 15 51749241 51749241 single base substitution C T downstream_gene_variant ESAD-UK 15 51749241 51749241 single base substitution C T intron_variant ESAD-UK 15 51749241 51749241 single base substitution C T upstream_gene_variant ESAD-UK 15 51752622 51752622 single base substitution G A downstream_gene_variant ESAD-UK 15 51752622 51752622 single base substitution G A intron_variant ESAD-UK 15 51752622 51752622 single base substitution G A upstream_gene_variant ESAD-UK 15 51755699 51755699 deletion of <=200bp A - intron_variant ESAD-UK 15 51755699 51755699 deletion of <=200bp A - splice_region_variant ESAD-UK 15 51755699 51755699 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 51756951 51756951 single base substitution G A exon_variant ESAD-UK 15 51756951 51756951 single base substitution G A intron_variant ESAD-UK 15 51756951 51756951 single base substitution G A missense_variant P1940S 5818C>T ESAD-UK 15 51756951 51756951 single base substitution G A missense_variant P2576S 7726C>T ESAD-UK 15 51756951 51756951 single base substitution G A missense_variant P2577S 7729C>T ESAD-UK 15 51756951 51756951 single base substitution G A missense_variant P701S 2101C>T ESAD-UK 15 51756951 51756951 single base substitution G A upstream_gene_variant ESAD-UK 15 51762523 51762523 single base substitution G A intron_variant ESAD-UK 15 51763047 51763047 single base substitution A T intron_variant ESAD-UK 15 51767766 51767766 deletion of <=200bp A - intron_variant ESAD-UK 15 51767766 51767766 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 51770465 51770465 single base substitution T A splice_region_variant ESAD-UK 15 51770868 51770868 single base substitution T C intron_variant ESAD-UK 15 51771292 51771292 single base substitution T A intron_variant ESAD-UK 15 51776263 51776263 single base substitution A G intron_variant ESAD-UK 15 51776263 51776263 single base substitution A G upstream_gene_variant ESAD-UK 15 51776714 51776714 single base substitution G A intron_variant ESAD-UK 15 51776714 51776714 single base substitution G A upstream_gene_variant ESAD-UK 15 51776927 51776927 single base substitution C T intron_variant ESAD-UK 15 51776927 51776927 single base substitution C T upstream_gene_variant ESAD-UK 15 51777407 51777407 single base substitution C A intron_variant ESAD-UK 15 51777407 51777407 single base substitution C A upstream_gene_variant ESAD-UK 15 51778255 51778255 single base substitution C T intron_variant ESAD-UK 15 51778255 51778255 single base substitution C T upstream_gene_variant ESAD-UK 15 51779590 51779590 single base substitution T A intron_variant ESAD-UK 15 51780095 51780095 single base substitution C T intron_variant ESAD-UK 15 51780621 51780621 single base substitution C T intron_variant ESAD-UK 15 51780786 51780786 single base substitution G A synonymous_variant Y1034Y 3102C>T ESAD-UK 15 51780786 51780786 single base substitution G A synonymous_variant Y1670Y 5010C>T ESAD-UK 15 51785299 51785299 single base substitution G A intron_variant ESAD-UK 15 51787690 51787690 single base substitution A G intron_variant ESAD-UK 15 51788392 51788392 single base substitution T G intron_variant ESAD-UK 15 51788890 51788890 single base substitution G A intron_variant ESAD-UK 15 51789861 51789861 single base substitution A C intron_variant ESAD-UK 15 51790662 51790662 single base substitution C T intron_variant ESAD-UK 15 51791659 51791659 single base substitution C T intron_variant ESAD-UK 15 51791659 51791659 single base substitution C T stop_gained W1254* 3762G>A ESAD-UK 15 51793383 51793383 single base substitution T G intron_variant ESAD-UK 15 51794810 51794810 single base substitution G A intron_variant ESAD-UK 15 51796534 51796534 single base substitution G A intron_variant ESAD-UK 15 51800091 51800091 single base substitution T A intron_variant ESAD-UK 15 51803127 51803127 single base substitution C G intron_variant ESAD-UK 15 51804174 51804174 single base substitution T G intron_variant ESAD-UK 15 51806133 51806146 deletion of <=200bp TACTTACTTTCACA - intron_variant ESAD-UK 15 51808402 51808402 single base substitution T C intron_variant ESAD-UK 15 51808746 51808746 single base substitution G A intron_variant ESAD-UK 15 51811507 51811507 single base substitution G A intron_variant ESAD-UK 15 51813245 51813245 single base substitution C T intron_variant ESAD-UK 15 51816919 51816919 single base substitution G A intron_variant ESAD-UK 15 51819358 51819358 single base substitution A G intron_variant ESAD-UK 15 51819417 51819417 single base substitution C T intron_variant ESAD-UK 15 51819606 51819606 insertion of <=200bp - A intron_variant ESAD-UK 15 51820765 51820765 single base substitution A T intron_variant ESAD-UK 15 51821405 51821408 deletion of <=200bp AAGC - intron_variant ESAD-UK 15 51821961 51821961 single base substitution G A intron_variant ESAD-UK 15 51824815 51824815 single base substitution A G intron_variant ESAD-UK 15 51824876 51824876 single base substitution T A intron_variant ESAD-UK 15 51824884 51824884 single base substitution T A intron_variant ESAD-UK 15 51826320 51826320 single base substitution C A intron_variant ESAD-UK 15 51827512 51827512 single base substitution A G intron_variant ESAD-UK 15 51828067 51828067 deletion of <=200bp T - intron_variant ESAD-UK 15 51828545 51828545 single base substitution G A missense_variant A711V 2132C>T ESAD-UK 15 51828546 51828546 single base substitution C G missense_variant A711P 2131G>C ESAD-UK 15 51829383 51829395 deletion of <=200bp GATTCACATTTTC - intron_variant ESAD-UK 15 51829756 51829756 single base substitution C A missense_variant D516Y 1546G>T ESAD-UK 15 51830271 51830271 single base substitution A T intron_variant ESAD-UK 15 51833477 51833477 single base substitution C T intron_variant ESAD-UK 15 51834005 51834005 single base substitution C T intron_variant ESAD-UK 15 51834217 51834217 single base substitution T C intron_variant ESAD-UK 15 51835050 51835050 single base substitution C A downstream_gene_variant ESAD-UK 15 51835050 51835050 single base substitution C A intron_variant ESAD-UK 15 51838047 51838047 single base substitution G C downstream_gene_variant ESAD-UK 15 51838047 51838047 single base substitution G C intron_variant ESAD-UK 15 51839498 51839498 single base substitution A C downstream_gene_variant ESAD-UK 15 51839498 51839498 single base substitution A C synonymous_variant S225S 675T>G ESAD-UK 15 51840376 51840376 single base substitution A G intron_variant ESAD-UK 15 51840602 51840602 deletion of <=200bp T - intron_variant ESAD-UK 15 51843900 51843900 single base substitution C T intron_variant ESAD-UK 15 51848815 51848815 single base substitution C G intron_variant ESAD-UK 15 51851054 51851054 single base substitution T C intron_variant ESAD-UK 15 51851491 51851491 single base substitution C A intron_variant ESAD-UK 15 51853397 51853397 single base substitution G T intron_variant ESAD-UK 15 51856313 51856313 single base substitution G A downstream_gene_variant ESAD-UK 15 51856313 51856313 single base substitution G A intron_variant ESAD-UK 15 51857323 51857323 insertion of <=200bp - A downstream_gene_variant ESAD-UK 15 51857323 51857323 insertion of <=200bp - A exon_variant ESAD-UK 15 51857323 51857323 insertion of <=200bp - A frameshift_variant L109F? ESAD-UK 15 51860972 51860972 single base substitution G A intron_variant ESAD-UK 15 51861412 51861412 single base substitution G A intron_variant ESAD-UK 15 51861680 51861680 single base substitution G T intron_variant ESAD-UK 15 51863310 51863310 deletion of <=200bp A - intron_variant ESAD-UK 15 51863336 51863336 single base substitution G C intron_variant ESAD-UK 15 51873708 51873708 single base substitution G T intron_variant ESAD-UK 15 51873867 51873867 single base substitution A G intron_variant ESAD-UK 15 51874644 51874644 single base substitution A G intron_variant ESAD-UK 15 51874890 51874890 single base substitution C T intron_variant ESAD-UK 15 51878390 51878390 single base substitution A G intron_variant ESAD-UK 15 51879227 51879227 single base substitution C T intron_variant ESAD-UK 15 51881806 51881806 single base substitution T C intron_variant ESAD-UK 15 51883755 51883755 single base substitution G A intron_variant ESAD-UK 15 51892739 51892739 single base substitution G A intron_variant ESAD-UK 15 51894525 51894525 deletion of <=200bp T - intron_variant ESAD-UK 15 51896991 51896991 deletion of <=200bp A - intron_variant ESAD-UK 15 51896991 51896991 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 51896999 51896999 single base substitution A G intron_variant ESAD-UK 15 51896999 51896999 single base substitution A G upstream_gene_variant ESAD-UK 15 51897499 51897499 single base substitution G C intron_variant ESAD-UK 15 51897499 51897499 single base substitution G C upstream_gene_variant ESAD-UK 15 51901379 51901379 single base substitution T C intron_variant ESAD-UK 15 51904265 51904265 single base substitution C T intron_variant ESAD-UK 15 51906655 51906655 single base substitution C A intron_variant ESAD-UK 15 51909622 51909622 single base substitution C T intron_variant ESAD-UK 15 51914985 51914985 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 15 51914985 51914985 single base substitution T A upstream_gene_variant ESAD-UK 15 51915275 51915275 single base substitution C T upstream_gene_variant ESAD-UK 15 51916877 51916877 single base substitution G T upstream_gene_variant ESAD-UK 15 51918575 51918575 single base substitution G A upstream_gene_variant ESAD-UK 15 51919342 51919342 single base substitution G A upstream_gene_variant ESAD-UK 15 51919897 51919897 single base substitution T A upstream_gene_variant ESCA-CN 15 51791278 51791278 single base substitution T A intron_variant ESCA-CN 15 51791278 51791278 single base substitution T A synonymous_variant I1381I 4143A>T ESCA-CN 15 51809399 51809399 insertion of <=200bp - A intron_variant ESCA-CN 15 51837855 51837855 single base substitution C G downstream_gene_variant ESCA-CN 15 51837855 51837855 single base substitution C G missense_variant E285D 855G>C ESCA-CN 15 51856581 51856581 single base substitution A T downstream_gene_variant ESCA-CN 15 51856581 51856581 single base substitution A T intron_variant KIRC-US 15 51741365 51741365 single base substitution A G downstream_gene_variant KIRC-US 15 51741365 51741365 single base substitution A G exon_variant KIRC-US 15 51741365 51741365 single base substitution A G missense_variant L1122P 3365T>C KIRC-US 15 51741365 51741365 single base substitution A G missense_variant L2340P 7019T>C KIRC-US 15 51741365 51741365 single base substitution A G missense_variant L2976P 8927T>C KIRC-US 15 51741365 51741365 single base substitution A G missense_variant L2977P 8930T>C KIRC-US 15 51773209 51773209 single base substitution C A missense_variant D1396Y 4186G>T KIRC-US 15 51773209 51773209 single base substitution C A missense_variant D156Y 466G>T KIRC-US 15 51773209 51773209 single base substitution C A missense_variant D2032Y 6094G>T KIRC-US 15 51778458 51778458 single base substitution G T stop_gained S1129* 3386C>A KIRC-US 15 51778458 51778458 single base substitution G T stop_gained S1765* 5294C>A KIRC-US 15 51778458 51778458 single base substitution G T upstream_gene_variant KIRC-US 15 51778460 51778460 single base substitution A G synonymous_variant T1128T 3384T>C KIRC-US 15 51778460 51778460 single base substitution A G synonymous_variant T1764T 5292T>C KIRC-US 15 51778460 51778460 single base substitution A G upstream_gene_variant KIRC-US 15 51790800 51790800 single base substitution C A intron_variant KIRC-US 15 51790800 51790800 single base substitution C A missense_variant V1541L 4621G>T KIRC-US 15 51837940 51837940 single base substitution A C downstream_gene_variant KIRC-US 15 51837940 51837940 single base substitution A C stop_gained L257* 770T>G KIRC-US 15 51839582 51839582 single base substitution C G exon_variant KIRC-US 15 51839582 51839582 single base substitution C G missense_variant W197C 591G>C KIRP-US 15 51773559 51773559 single base substitution G A missense_variant S1279F 3836C>T KIRP-US 15 51773559 51773559 single base substitution G A missense_variant S1915F 5744C>T KIRP-US 15 51773559 51773559 single base substitution G A missense_variant S39F 116C>T KIRP-US 15 51783908 51783908 single base substitution G A missense_variant S1607F 4820C>T KIRP-US 15 51783908 51783908 single base substitution G A missense_variant S971F 2912C>T KIRP-US 15 51790750 51790750 single base substitution T G intron_variant KIRP-US 15 51790750 51790750 single base substitution T G splice_region_variant KIRP-US 15 51828388 51828388 single base substitution T G synonymous_variant P763P 2289A>C LAML-KR 15 51748081 51748081 single base substitution A G downstream_gene_variant LAML-KR 15 51748081 51748081 single base substitution A G intron_variant LAML-KR 15 51748081 51748081 single base substitution A G upstream_gene_variant LAML-KR 15 51788341 51788341 single base substitution C T intron_variant LAML-KR 15 51801635 51801635 single base substitution A C intron_variant LGG-US 15 51766595 51766595 single base substitution C T missense_variant G1750R 5248G>A LGG-US 15 51766595 51766595 single base substitution C T missense_variant G2386R 7156G>A LGG-US 15 51766595 51766595 single base substitution C T missense_variant G2387R 7159G>A LGG-US 15 51766595 51766595 single base substitution C T missense_variant G511R 1531G>A LGG-US 15 51766595 51766595 single base substitution C T upstream_gene_variant LGG-US 15 51773679 51773679 single base substitution T C missense_variant D1239G 3716A>G LGG-US 15 51773679 51773679 single base substitution T C missense_variant D1875G 5624A>G LGG-US 15 51773679 51773679 single base substitution T C upstream_gene_variant LGG-US 15 51791722 51791724 deletion of <=200bp AAG - inframe_deletion L1233 LGG-US 15 51791722 51791724 deletion of <=200bp AAG - intron_variant LICA-CN 15 51742507 51742507 single base substitution T A downstream_gene_variant LICA-CN 15 51742507 51742507 single base substitution T A exon_variant LICA-CN 15 51742507 51742507 single base substitution T A missense_variant Q1053L 3158A>T LICA-CN 15 51742507 51742507 single base substitution T A missense_variant Q2271L 6812A>T LICA-CN 15 51742507 51742507 single base substitution T A missense_variant Q2907L 8720A>T LICA-CN 15 51742507 51742507 single base substitution T A missense_variant Q2908L 8723A>T LICA-CN 15 51742507 51742507 single base substitution T A synonymous_variant A64A 192A>T LICA-CN 15 51757827 51757827 single base substitution T A exon_variant LICA-CN 15 51757827 51757827 single base substitution T A synonymous_variant T1877T 5631A>T LICA-CN 15 51757827 51757827 single base substitution T A synonymous_variant T2513T 7539A>T LICA-CN 15 51757827 51757827 single base substitution T A synonymous_variant T2514T 7542A>T LICA-CN 15 51757827 51757827 single base substitution T A synonymous_variant T638T 1914A>T LICA-CN 15 51773070 51773070 single base substitution T A missense_variant E1442V 4325A>T LICA-CN 15 51773070 51773070 single base substitution T A missense_variant E202V 605A>T LICA-CN 15 51773070 51773070 single base substitution T A missense_variant E2078V 6233A>T LICA-CN 15 51780764 51780764 single base substitution C A missense_variant V1042L 3124G>T LICA-CN 15 51780764 51780764 single base substitution C A missense_variant V1678L 5032G>T LICA-CN 15 51791126 51791126 single base substitution T C intron_variant LICA-CN 15 51791126 51791126 single base substitution T C missense_variant Y1432C 4295A>G LICA-CN 15 51791776 51791776 single base substitution A G intron_variant LICA-CN 15 51791776 51791776 single base substitution A G synonymous_variant T1215T 3645T>C LICA-CN 15 51792224 51792224 single base substitution C T intron_variant LICA-CN 15 51792224 51792224 single base substitution C T missense_variant S1066N 3197G>A LICA-FR 15 51739293 51739293 single base substitution A G downstream_gene_variant LICA-FR 15 51779866 51779866 single base substitution G A intron_variant LICA-FR 15 51780745 51780745 single base substitution C T missense_variant R1048K 3143G>A LICA-FR 15 51780745 51780745 single base substitution C T missense_variant R1684K 5051G>A LICA-FR 15 51788273 51788273 single base substitution C T intron_variant LICA-FR 15 51791834 51791834 single base substitution C T intron_variant LICA-FR 15 51791834 51791834 single base substitution C T missense_variant R1196K 3587G>A LICA-FR 15 51795965 51795965 single base substitution T A intron_variant LICA-FR 15 51796423 51796423 deletion of <=200bp G - intron_variant LICA-FR 15 51797087 51797087 single base substitution C A intron_variant LICA-FR 15 51813191 51813191 single base substitution T C intron_variant LICA-FR 15 51817316 51817316 single base substitution C A intron_variant LICA-FR 15 51829060 51829060 single base substitution C T splice_acceptor_variant LICA-FR 15 51829119 51829119 single base substitution T A intron_variant LICA-FR 15 51886453 51886453 single base substitution A G intron_variant LICA-FR 15 51886462 51886462 single base substitution C A intron_variant LICA-FR 15 51887132 51887132 single base substitution T C intron_variant LICA-FR 15 51888047 51888047 single base substitution G A intron_variant LICA-FR 15 51890867 51890867 single base substitution C T intron_variant LIHC-US 15 51748508 51748508 single base substitution T C downstream_gene_variant LIHC-US 15 51748508 51748508 single base substitution T C missense_variant Y2141C 6422A>G LIHC-US 15 51748508 51748508 single base substitution T C missense_variant Y2777C 8330A>G LIHC-US 15 51748508 51748508 single base substitution T C missense_variant Y2778C 8333A>G LIHC-US 15 51748508 51748508 single base substitution T C missense_variant Y923C 2768A>G LIHC-US 15 51748508 51748508 single base substitution T C splice_region_variant LIHC-US 15 51748508 51748508 single base substitution T C upstream_gene_variant LIHC-US 15 51756896 51756896 single base substitution A C exon_variant LIHC-US 15 51756896 51756896 single base substitution A C intron_variant LIHC-US 15 51756896 51756896 single base substitution A C missense_variant L1958R 5873T>G LIHC-US 15 51756896 51756896 single base substitution A C missense_variant L2594R 7781T>G LIHC-US 15 51756896 51756896 single base substitution A C missense_variant L2595R 7784T>G LIHC-US 15 51756896 51756896 single base substitution A C missense_variant L719R 2156T>G LIHC-US 15 51756896 51756896 single base substitution A C upstream_gene_variant LIHC-US 15 51757753 51757761 deletion of <=200bp CCAAACTCA - splice_donor_variant LIHC-US 15 51791589 51791589 single base substitution C G intron_variant LIHC-US 15 51791589 51791589 single base substitution C G missense_variant V1278L 3832G>C LIHC-US 15 51828802 51828802 single base substitution T A synonymous_variant A625A 1875A>T LIHC-US 15 51839582 51839582 single base substitution C T exon_variant LIHC-US 15 51839582 51839582 single base substitution C T stop_gained W197* 591G>A LIHC-US 15 51868294 51868294 single base substitution T C exon_variant LIHC-US 15 51868294 51868294 single base substitution T C missense_variant I58V 172A>G LINC-JP 15 51735269 51735269 single base substitution T A downstream_gene_variant LINC-JP 15 51740678 51740678 single base substitution C T 3_prime_UTR_variant LINC-JP 15 51740678 51740678 single base substitution C T downstream_gene_variant LINC-JP 15 51740678 51740678 single base substitution C T exon_variant LINC-JP 15 51741320 51741320 single base substitution C T downstream_gene_variant LINC-JP 15 51741320 51741320 single base substitution C T exon_variant LINC-JP 15 51741320 51741320 single base substitution C T missense_variant R1137Q 3410G>A LINC-JP 15 51741320 51741320 single base substitution C T missense_variant R2355Q 7064G>A LINC-JP 15 51741320 51741320 single base substitution C T missense_variant R2991Q 8972G>A LINC-JP 15 51741320 51741320 single base substitution C T missense_variant R2992Q 8975G>A LINC-JP 15 51747602 51747602 single base substitution T A downstream_gene_variant LINC-JP 15 51747602 51747602 single base substitution T A intron_variant LINC-JP 15 51747602 51747602 single base substitution T A upstream_gene_variant LINC-JP 15 51750816 51750816 single base substitution A G 3_prime_UTR_variant LINC-JP 15 51750816 51750816 single base substitution A G downstream_gene_variant LINC-JP 15 51750816 51750816 single base substitution A G exon_variant LINC-JP 15 51750816 51750816 single base substitution A G synonymous_variant C2037C 6111T>C LINC-JP 15 51750816 51750816 single base substitution A G synonymous_variant C2673C 8019T>C LINC-JP 15 51750816 51750816 single base substitution A G synonymous_variant C2674C 8022T>C LINC-JP 15 51750816 51750816 single base substitution A G synonymous_variant C819C 2457T>C LINC-JP 15 51750816 51750816 single base substitution A G upstream_gene_variant LINC-JP 15 51750868 51750868 single base substitution A C downstream_gene_variant LINC-JP 15 51750868 51750868 single base substitution A C exon_variant LINC-JP 15 51750868 51750868 single base substitution A C intron_variant LINC-JP 15 51750868 51750868 single base substitution A C upstream_gene_variant LINC-JP 15 51751543 51751543 single base substitution A T downstream_gene_variant LINC-JP 15 51751543 51751543 single base substitution A T intron_variant LINC-JP 15 51751543 51751543 single base substitution A T upstream_gene_variant LINC-JP 15 51772119 51772119 single base substitution T C intron_variant LINC-JP 15 51772961 51772961 single base substitution T C synonymous_variant E1478E 4434A>G LINC-JP 15 51772961 51772961 single base substitution T C synonymous_variant E2114E 6342A>G LINC-JP 15 51772961 51772961 single base substitution T C synonymous_variant E238E 714A>G LINC-JP 15 51783806 51783806 single base substitution T G missense_variant N1005T 3014A>C LINC-JP 15 51783806 51783806 single base substitution T G missense_variant N1641T 4922A>C LINC-JP 15 51787256 51787256 single base substitution A T missense_variant L1583Q 4748T>A LINC-JP 15 51787256 51787256 single base substitution A T missense_variant L947Q 2840T>A LINC-JP 15 51791054 51791054 single base substitution T C intron_variant LINC-JP 15 51791054 51791054 single base substitution T C missense_variant Y1456C 4367A>G LINC-JP 15 51825180 51825180 single base substitution C T intron_variant LINC-JP 15 51836287 51836287 single base substitution T C downstream_gene_variant LINC-JP 15 51836287 51836287 single base substitution T C intron_variant LINC-JP 15 51849259 51849259 single base substitution A G intron_variant LINC-JP 15 51853351 51853351 single base substitution T C intron_variant LINC-JP 15 51857685 51857685 single base substitution C A downstream_gene_variant LINC-JP 15 51857685 51857685 single base substitution C A intron_variant LINC-JP 15 51868338 51868338 single base substitution T C exon_variant LINC-JP 15 51868338 51868338 single base substitution T C missense_variant D43G 128A>G LINC-JP 15 51871319 51871319 single base substitution G A intron_variant LINC-JP 15 51910461 51910461 single base substitution C T intron_variant LINC-JP 15 51911550 51911550 single base substitution T C intron_variant LIRI-JP 15 51734941 51734941 single base substitution T C downstream_gene_variant LIRI-JP 15 51736926 51736926 single base substitution T A downstream_gene_variant LIRI-JP 15 51738587 51738587 single base substitution C T downstream_gene_variant LIRI-JP 15 51739383 51739383 single base substitution G A downstream_gene_variant LIRI-JP 15 51739403 51739403 single base substitution C A downstream_gene_variant LIRI-JP 15 51739912 51739912 single base substitution T C 3_prime_UTR_variant LIRI-JP 15 51739912 51739912 single base substitution T C downstream_gene_variant LIRI-JP 15 51741802 51741802 single base substitution C A downstream_gene_variant LIRI-JP 15 51741802 51741802 single base substitution C A intron_variant LIRI-JP 15 51743345 51743345 single base substitution C T downstream_gene_variant LIRI-JP 15 51743345 51743345 single base substitution C T intron_variant LIRI-JP 15 51743345 51743345 single base substitution C T upstream_gene_variant LIRI-JP 15 51743555 51743555 single base substitution T C downstream_gene_variant LIRI-JP 15 51743555 51743555 single base substitution T C intron_variant LIRI-JP 15 51743555 51743555 single base substitution T C upstream_gene_variant LIRI-JP 15 51744709 51744709 single base substitution C T downstream_gene_variant LIRI-JP 15 51744709 51744709 single base substitution C T intron_variant LIRI-JP 15 51744709 51744709 single base substitution C T upstream_gene_variant LIRI-JP 15 51745809 51745809 single base substitution A G downstream_gene_variant LIRI-JP 15 51745809 51745809 single base substitution A G exon_variant LIRI-JP 15 51745809 51745809 single base substitution A G synonymous_variant S1002S 3006T>C LIRI-JP 15 51745809 51745809 single base substitution A G synonymous_variant S2220S 6660T>C LIRI-JP 15 51745809 51745809 single base substitution A G synonymous_variant S2856S 8568T>C LIRI-JP 15 51745809 51745809 single base substitution A G synonymous_variant S2857S 8571T>C LIRI-JP 15 51745809 51745809 single base substitution A G synonymous_variant S31S 93T>C LIRI-JP 15 51745809 51745809 single base substitution A G upstream_gene_variant LIRI-JP 15 51751933 51751933 single base substitution G A downstream_gene_variant LIRI-JP 15 51751933 51751933 single base substitution G A exon_variant LIRI-JP 15 51751933 51751933 single base substitution G A intron_variant LIRI-JP 15 51751933 51751933 single base substitution G A upstream_gene_variant LIRI-JP 15 51751934 51751934 single base substitution C A downstream_gene_variant LIRI-JP 15 51751934 51751934 single base substitution C A exon_variant LIRI-JP 15 51751934 51751934 single base substitution C A intron_variant LIRI-JP 15 51751934 51751934 single base substitution C A upstream_gene_variant LIRI-JP 15 51752743 51752743 single base substitution G C downstream_gene_variant LIRI-JP 15 51752743 51752743 single base substitution G C intron_variant LIRI-JP 15 51752743 51752743 single base substitution G C upstream_gene_variant LIRI-JP 15 51756458 51756458 single base substitution C T intron_variant LIRI-JP 15 51756458 51756458 single base substitution C T upstream_gene_variant LIRI-JP 15 51758003 51758003 single base substitution C A intron_variant LIRI-JP 15 51758753 51758753 single base substitution A G intron_variant LIRI-JP 15 51759602 51759602 single base substitution C G intron_variant LIRI-JP 15 51759916 51759916 single base substitution C T intron_variant LIRI-JP 15 51760900 51760900 single base substitution T A intron_variant LIRI-JP 15 51764151 51764151 single base substitution T C intron_variant LIRI-JP 15 51764151 51764151 single base substitution T C upstream_gene_variant LIRI-JP 15 51764323 51764323 single base substitution A C intron_variant LIRI-JP 15 51764323 51764323 single base substitution A C upstream_gene_variant LIRI-JP 15 51766456 51766456 single base substitution T C intron_variant LIRI-JP 15 51766456 51766456 single base substitution T C upstream_gene_variant LIRI-JP 15 51768496 51768496 single base substitution T C intron_variant LIRI-JP 15 51768496 51768496 single base substitution T C upstream_gene_variant LIRI-JP 15 51768594 51768594 single base substitution A G intron_variant LIRI-JP 15 51772046 51772046 single base substitution A G intron_variant LIRI-JP 15 51772159 51772159 single base substitution T C missense_variant I1612V 4834A>G LIRI-JP 15 51772159 51772159 single base substitution T C missense_variant I2248V 6742A>G LIRI-JP 15 51772159 51772159 single base substitution T C missense_variant I372V 1114A>G LIRI-JP 15 51773615 51773615 single base substitution T C synonymous_variant G1260G 3780A>G LIRI-JP 15 51773615 51773615 single base substitution T C synonymous_variant G1896G 5688A>G LIRI-JP 15 51773615 51773615 single base substitution T C synonymous_variant G20G 60A>G LIRI-JP 15 51774099 51774099 single base substitution C G intron_variant LIRI-JP 15 51774099 51774099 single base substitution C G upstream_gene_variant LIRI-JP 15 51774858 51774858 single base substitution A T intron_variant LIRI-JP 15 51774858 51774858 single base substitution A T upstream_gene_variant LIRI-JP 15 51775447 51775447 single base substitution T C intron_variant LIRI-JP 15 51775447 51775447 single base substitution T C upstream_gene_variant LIRI-JP 15 51779585 51779585 single base substitution A C intron_variant LIRI-JP 15 51779845 51779845 single base substitution G C intron_variant LIRI-JP 15 51779906 51779906 single base substitution T C intron_variant LIRI-JP 15 51781370 51781370 single base substitution G A intron_variant LIRI-JP 15 51781669 51781669 single base substitution C T intron_variant LIRI-JP 15 51782205 51782205 single base substitution T C intron_variant LIRI-JP 15 51784611 51784611 deletion of <=200bp T - intron_variant LIRI-JP 15 51784643 51784643 single base substitution C T intron_variant LIRI-JP 15 51785105 51785105 single base substitution T C intron_variant LIRI-JP 15 51787217 51787217 single base substitution T G splice_region_variant LIRI-JP 15 51787817 51787817 single base substitution C A intron_variant LIRI-JP 15 51789514 51789514 single base substitution A G intron_variant LIRI-JP 15 51789572 51789572 single base substitution A T intron_variant LIRI-JP 15 51790388 51790388 single base substitution G T intron_variant LIRI-JP 15 51791432 51791432 single base substitution T C intron_variant LIRI-JP 15 51791432 51791432 single base substitution T C missense_variant D1330G 3989A>G LIRI-JP 15 51791798 51791798 single base substitution T G intron_variant LIRI-JP 15 51791798 51791798 single base substitution T G missense_variant K1208T 3623A>C LIRI-JP 15 51791868 51791868 single base substitution C T intron_variant LIRI-JP 15 51791868 51791868 single base substitution C T missense_variant V1185M 3553G>A LIRI-JP 15 51794644 51794644 single base substitution C A intron_variant LIRI-JP 15 51797730 51797730 single base substitution G T intron_variant LIRI-JP 15 51798089 51798089 single base substitution C T intron_variant LIRI-JP 15 51798852 51798852 single base substitution A C intron_variant LIRI-JP 15 51799684 51799684 single base substitution T C intron_variant LIRI-JP 15 51799992 51799992 single base substitution T C intron_variant LIRI-JP 15 51800280 51800280 single base substitution A C intron_variant LIRI-JP 15 51803097 51803097 single base substitution C T intron_variant LIRI-JP 15 51805870 51805870 single base substitution T C intron_variant LIRI-JP 15 51805899 51805899 single base substitution T C intron_variant LIRI-JP 15 51807124 51807124 single base substitution G A intron_variant LIRI-JP 15 51808010 51808010 insertion of <=200bp - A intron_variant LIRI-JP 15 51808481 51808481 single base substitution T C intron_variant LIRI-JP 15 51811997 51811997 single base substitution A G intron_variant LIRI-JP 15 51816085 51816085 single base substitution C A intron_variant LIRI-JP 15 51816339 51816339 single base substitution A G intron_variant LIRI-JP 15 51817203 51817203 single base substitution G C intron_variant LIRI-JP 15 51820665 51820665 single base substitution T G intron_variant LIRI-JP 15 51821167 51821167 single base substitution C T intron_variant LIRI-JP 15 51822886 51822886 single base substitution C T intron_variant LIRI-JP 15 51824130 51824130 single base substitution A G intron_variant LIRI-JP 15 51825534 51825534 single base substitution A G intron_variant LIRI-JP 15 51826290 51826290 single base substitution G A intron_variant LIRI-JP 15 51826992 51826992 single base substitution C G intron_variant LIRI-JP 15 51827011 51827011 single base substitution C T intron_variant LIRI-JP 15 51829569 51829569 single base substitution G A intron_variant LIRI-JP 15 51830764 51830764 single base substitution T C intron_variant LIRI-JP 15 51830867 51830867 insertion of <=200bp - A intron_variant LIRI-JP 15 51832728 51832728 single base substitution A C intron_variant LIRI-JP 15 51840436 51840436 single base substitution T C intron_variant LIRI-JP 15 51843011 51843011 single base substitution C T intron_variant LIRI-JP 15 51843682 51843682 single base substitution T A intron_variant LIRI-JP 15 51844946 51844946 single base substitution A T intron_variant LIRI-JP 15 51849674 51849674 single base substitution A G intron_variant LIRI-JP 15 51850131 51850131 single base substitution G C intron_variant LIRI-JP 15 51850797 51850797 single base substitution T C intron_variant LIRI-JP 15 51851876 51851876 single base substitution C A intron_variant LIRI-JP 15 51853324 51853324 single base substitution G T intron_variant LIRI-JP 15 51853483 51853483 single base substitution T C intron_variant LIRI-JP 15 51853948 51853948 single base substitution A C intron_variant LIRI-JP 15 51854366 51854366 single base substitution A G downstream_gene_variant LIRI-JP 15 51854366 51854366 single base substitution A G intron_variant LIRI-JP 15 51855660 51855660 single base substitution T G downstream_gene_variant LIRI-JP 15 51855660 51855660 single base substitution T G intron_variant LIRI-JP 15 51857282 51857282 single base substitution T C downstream_gene_variant LIRI-JP 15 51857282 51857282 single base substitution T C splice_region_variant LIRI-JP 15 51857819 51857819 single base substitution T C downstream_gene_variant LIRI-JP 15 51857819 51857819 single base substitution T C intron_variant LIRI-JP 15 51861531 51861531 single base substitution C A intron_variant LIRI-JP 15 51861641 51861641 single base substitution C A intron_variant LIRI-JP 15 51865919 51865919 single base substitution T C intron_variant LIRI-JP 15 51870144 51870144 single base substitution C T intron_variant LIRI-JP 15 51871249 51871249 single base substitution C T intron_variant LIRI-JP 15 51873794 51873794 single base substitution C A intron_variant LIRI-JP 15 51874931 51874931 single base substitution T C intron_variant LIRI-JP 15 51877597 51877597 single base substitution T A intron_variant LIRI-JP 15 51877811 51877811 single base substitution A C intron_variant LIRI-JP 15 51877815 51877815 single base substitution A G intron_variant LIRI-JP 15 51879323 51879323 single base substitution T C intron_variant LIRI-JP 15 51881680 51881680 single base substitution G A intron_variant LIRI-JP 15 51884552 51884552 single base substitution G C intron_variant LIRI-JP 15 51886614 51886614 single base substitution T C intron_variant LIRI-JP 15 51887689 51887689 single base substitution C T intron_variant LIRI-JP 15 51894217 51894217 single base substitution G A intron_variant LIRI-JP 15 51895802 51895802 single base substitution G A intron_variant LIRI-JP 15 51895802 51895802 single base substitution G A splice_donor_variant LIRI-JP 15 51898041 51898041 insertion of <=200bp - ATA intron_variant LIRI-JP 15 51898041 51898041 insertion of <=200bp - ATA upstream_gene_variant LIRI-JP 15 51898217 51898217 single base substitution A G intron_variant LIRI-JP 15 51898217 51898217 single base substitution A G upstream_gene_variant LIRI-JP 15 51898546 51898546 single base substitution G A intron_variant LIRI-JP 15 51898546 51898546 single base substitution G A upstream_gene_variant LIRI-JP 15 51899966 51899966 single base substitution T A intron_variant LIRI-JP 15 51899966 51899966 single base substitution T A upstream_gene_variant LIRI-JP 15 51901187 51901187 single base substitution T C intron_variant LIRI-JP 15 51902208 51902208 single base substitution T C intron_variant LIRI-JP 15 51902249 51902249 single base substitution T A intron_variant LIRI-JP 15 51902250 51902250 single base substitution T A intron_variant LIRI-JP 15 51902367 51902367 single base substitution C T intron_variant LIRI-JP 15 51903901 51903901 single base substitution T C intron_variant LIRI-JP 15 51904144 51904144 single base substitution G A intron_variant LIRI-JP 15 51905513 51905513 single base substitution G A intron_variant LIRI-JP 15 51907702 51907702 single base substitution C T intron_variant LIRI-JP 15 51908234 51908236 deletion of <=200bp AAC - intron_variant LIRI-JP 15 51912221 51912221 single base substitution G A intron_variant LIRI-JP 15 51913512 51913512 single base substitution T C intron_variant LIRI-JP 15 51915119 51915119 single base substitution G A upstream_gene_variant LIRI-JP 15 51915711 51915711 single base substitution T G upstream_gene_variant LIRI-JP 15 51918457 51918457 single base substitution C T upstream_gene_variant LUSC-KR 15 51735852 51735852 single base substitution G C downstream_gene_variant LUSC-KR 15 51738466 51738466 single base substitution C A downstream_gene_variant LUSC-KR 15 51748583 51748583 single base substitution T A downstream_gene_variant LUSC-KR 15 51748583 51748583 single base substitution T A intron_variant LUSC-KR 15 51748583 51748583 single base substitution T A upstream_gene_variant LUSC-KR 15 51749474 51749474 single base substitution G A downstream_gene_variant LUSC-KR 15 51749474 51749474 single base substitution G A intron_variant LUSC-KR 15 51749474 51749474 single base substitution G A upstream_gene_variant LUSC-KR 15 51749762 51749762 single base substitution T G intron_variant LUSC-KR 15 51749762 51749762 single base substitution T G upstream_gene_variant LUSC-KR 15 51751300 51751300 single base substitution C T downstream_gene_variant LUSC-KR 15 51751300 51751300 single base substitution C T exon_variant LUSC-KR 15 51751300 51751300 single base substitution C T intron_variant LUSC-KR 15 51751300 51751300 single base substitution C T upstream_gene_variant LUSC-KR 15 51761071 51761071 single base substitution G A intron_variant LUSC-KR 15 51773357 51773357 single base substitution G A synonymous_variant H106H 318C>T LUSC-KR 15 51773357 51773357 single base substitution G A synonymous_variant H1346H 4038C>T LUSC-KR 15 51773357 51773357 single base substitution G A synonymous_variant H1982H 5946C>T LUSC-KR 15 51774634 51774634 single base substitution C A intron_variant LUSC-KR 15 51774634 51774634 single base substitution C A upstream_gene_variant LUSC-KR 15 51780371 51780371 single base substitution G A intron_variant LUSC-KR 15 51785507 51785507 single base substitution C T intron_variant LUSC-KR 15 51788885 51788885 single base substitution G A intron_variant LUSC-KR 15 51794153 51794153 single base substitution C A intron_variant LUSC-KR 15 51794194 51794194 single base substitution G T intron_variant LUSC-KR 15 51797299 51797299 single base substitution A C intron_variant LUSC-KR 15 51798963 51798963 single base substitution T G intron_variant LUSC-KR 15 51801617 51801617 single base substitution T A intron_variant LUSC-KR 15 51801635 51801635 single base substitution A C intron_variant LUSC-KR 15 51803518 51803518 single base substitution T G intron_variant LUSC-KR 15 51808332 51808332 single base substitution T G intron_variant LUSC-KR 15 51810940 51810940 single base substitution T C intron_variant LUSC-KR 15 51814208 51814208 single base substitution T C intron_variant LUSC-KR 15 51820641 51820641 single base substitution T C intron_variant LUSC-KR 15 51824133 51824133 single base substitution A G intron_variant LUSC-KR 15 51825642 51825642 single base substitution C A intron_variant LUSC-KR 15 51826948 51826948 single base substitution C A intron_variant LUSC-KR 15 51827416 51827416 single base substitution G A intron_variant LUSC-KR 15 51835056 51835056 single base substitution T A downstream_gene_variant LUSC-KR 15 51835056 51835056 single base substitution T A intron_variant LUSC-KR 15 51838680 51838680 single base substitution C G downstream_gene_variant LUSC-KR 15 51838680 51838680 single base substitution C G intron_variant LUSC-KR 15 51840766 51840766 single base substitution T C intron_variant LUSC-KR 15 51842542 51842542 single base substitution C A intron_variant LUSC-KR 15 51855705 51855705 single base substitution T C downstream_gene_variant LUSC-KR 15 51855705 51855705 single base substitution T C intron_variant LUSC-KR 15 51856143 51856143 single base substitution T C downstream_gene_variant LUSC-KR 15 51856143 51856143 single base substitution T C intron_variant LUSC-KR 15 51861841 51861841 single base substitution T C intron_variant LUSC-KR 15 51868614 51868614 single base substitution G A intron_variant LUSC-KR 15 51872100 51872100 single base substitution C A intron_variant LUSC-KR 15 51876309 51876309 single base substitution G A intron_variant LUSC-KR 15 51876535 51876535 single base substitution C G intron_variant LUSC-KR 15 51876611 51876611 single base substitution G A intron_variant LUSC-KR 15 51876650 51876650 single base substitution T C intron_variant LUSC-KR 15 51878373 51878373 single base substitution C T intron_variant LUSC-KR 15 51882163 51882163 single base substitution T A intron_variant LUSC-KR 15 51883601 51883601 single base substitution C A intron_variant LUSC-KR 15 51884971 51884971 single base substitution G C intron_variant LUSC-KR 15 51888164 51888164 single base substitution C A intron_variant LUSC-KR 15 51888510 51888510 single base substitution T C intron_variant LUSC-KR 15 51890192 51890192 single base substitution G C intron_variant LUSC-KR 15 51907914 51907914 single base substitution G T intron_variant LUSC-US 15 51750748 51750748 single base substitution T A 3_prime_UTR_variant LUSC-US 15 51750748 51750748 single base substitution T A downstream_gene_variant LUSC-US 15 51750748 51750748 single base substitution T A exon_variant LUSC-US 15 51750748 51750748 single base substitution T A missense_variant Q2060L 6179A>T LUSC-US 15 51750748 51750748 single base substitution T A missense_variant Q2696L 8087A>T LUSC-US 15 51750748 51750748 single base substitution T A missense_variant Q2697L 8090A>T LUSC-US 15 51750748 51750748 single base substitution T A missense_variant Q842L 2525A>T LUSC-US 15 51750748 51750748 single base substitution T A upstream_gene_variant LUSC-US 15 51755631 51755631 single base substitution A G exon_variant LUSC-US 15 51755631 51755631 single base substitution A G intron_variant LUSC-US 15 51755631 51755631 single base substitution A G missense_variant V1987A 5960T>C LUSC-US 15 51755631 51755631 single base substitution A G missense_variant V2623A 7868T>C LUSC-US 15 51755631 51755631 single base substitution A G missense_variant V2624A 7871T>C LUSC-US 15 51755631 51755631 single base substitution A G missense_variant V748A 2243T>C LUSC-US 15 51755631 51755631 single base substitution A G upstream_gene_variant LUSC-US 15 51757049 51757049 single base substitution C A exon_variant LUSC-US 15 51757049 51757049 single base substitution C A intron_variant LUSC-US 15 51757049 51757049 single base substitution C A missense_variant G1907V 5720G>T LUSC-US 15 51757049 51757049 single base substitution C A missense_variant G2543V 7628G>T LUSC-US 15 51757049 51757049 single base substitution C A missense_variant G2544V 7631G>T LUSC-US 15 51757049 51757049 single base substitution C A missense_variant G668V 2003G>T LUSC-US 15 51792045 51792045 single base substitution C T intron_variant LUSC-US 15 51792045 51792045 single base substitution C T missense_variant D1126N 3376G>A LUSC-US 15 51828679 51828679 single base substitution C G missense_variant L666F 1998G>C LUSC-US 15 51828946 51828946 single base substitution C A synonymous_variant T577T 1731G>T LUSC-US 15 51828999 51828999 single base substitution T C missense_variant K560E 1678A>G LUSC-US 15 51830482 51830482 single base substitution C A missense_variant D425Y 1273G>T LUSC-US 15 51830483 51830483 single base substitution A C missense_variant D424E 1272T>G LUSC-US 15 51839432 51839432 single base substitution C A downstream_gene_variant LUSC-US 15 51839432 51839432 single base substitution C A missense_variant M247I 741G>T LUSC-US 15 51839475 51839475 single base substitution C T downstream_gene_variant LUSC-US 15 51839475 51839475 single base substitution C T missense_variant R233Q 698G>A MALY-DE 15 51737832 51737832 deletion of <=200bp T - downstream_gene_variant MALY-DE 15 51750132 51750132 single base substitution G A intron_variant MALY-DE 15 51750132 51750132 single base substitution G A upstream_gene_variant MALY-DE 15 51751459 51751459 single base substitution T C downstream_gene_variant MALY-DE 15 51751459 51751459 single base substitution T C intron_variant MALY-DE 15 51751459 51751459 single base substitution T C upstream_gene_variant MALY-DE 15 51759459 51759459 single base substitution T C intron_variant MALY-DE 15 51759750 51759750 single base substitution C T intron_variant MALY-DE 15 51764180 51764180 single base substitution T C intron_variant MALY-DE 15 51764180 51764180 single base substitution T C upstream_gene_variant MALY-DE 15 51770325 51770325 single base substitution T C intron_variant MALY-DE 15 51773472 51773472 single base substitution C G missense_variant G1308A 3923G>C MALY-DE 15 51773472 51773472 single base substitution C G missense_variant G1944A 5831G>C MALY-DE 15 51773472 51773472 single base substitution C G missense_variant G68A 203G>C MALY-DE 15 51793186 51793186 single base substitution G C intron_variant MALY-DE 15 51796061 51796061 single base substitution A T intron_variant MALY-DE 15 51797658 51797658 single base substitution C A intron_variant MALY-DE 15 51798939 51798939 single base substitution C T intron_variant MALY-DE 15 51798971 51798971 single base substitution G T intron_variant MALY-DE 15 51802708 51802708 single base substitution G T intron_variant MALY-DE 15 51813659 51813661 deletion of <=200bp GTG - intron_variant MALY-DE 15 51814350 51814350 single base substitution A T intron_variant MALY-DE 15 51815250 51815250 single base substitution A C intron_variant MALY-DE 15 51816755 51816755 single base substitution C A intron_variant MALY-DE 15 51819768 51819768 insertion of <=200bp - AAAT intron_variant MALY-DE 15 51823086 51823086 deletion of <=200bp A - intron_variant MALY-DE 15 51824883 51824883 single base substitution A T intron_variant MALY-DE 15 51827080 51827080 single base substitution C T intron_variant MALY-DE 15 51837209 51837209 single base substitution C T downstream_gene_variant MALY-DE 15 51837209 51837209 single base substitution C T intron_variant MALY-DE 15 51844824 51844824 single base substitution C T intron_variant MALY-DE 15 51846777 51846777 single base substitution T C intron_variant MALY-DE 15 51850591 51850591 single base substitution A C intron_variant MALY-DE 15 51852625 51852625 single base substitution A T intron_variant MALY-DE 15 51856777 51856777 single base substitution C T downstream_gene_variant MALY-DE 15 51856777 51856777 single base substitution C T intron_variant MALY-DE 15 51857857 51857857 single base substitution G A downstream_gene_variant MALY-DE 15 51857857 51857857 single base substitution G A intron_variant MALY-DE 15 51860536 51860536 single base substitution A C exon_variant MALY-DE 15 51860536 51860536 single base substitution A C intron_variant MALY-DE 15 51864307 51864307 single base substitution A C intron_variant MALY-DE 15 51882765 51882765 deletion of <=200bp T - intron_variant MALY-DE 15 51893964 51893964 single base substitution A C intron_variant MALY-DE 15 51898074 51898074 single base substitution A G intron_variant MALY-DE 15 51898074 51898074 single base substitution A G upstream_gene_variant MALY-DE 15 51900960 51900960 deletion of <=200bp A - intron_variant MALY-DE 15 51901898 51901898 single base substitution G A intron_variant MALY-DE 15 51906985 51906985 insertion of <=200bp - G intron_variant MALY-DE 15 51907603 51907603 single base substitution T G intron_variant MALY-DE 15 51910754 51910754 insertion of <=200bp - A intron_variant MALY-DE 15 51918533 51918533 single base substitution T G upstream_gene_variant MELA-AU 15 51734924 51734924 single base substitution C G downstream_gene_variant MELA-AU 15 51735233 51735233 single base substitution G A downstream_gene_variant MELA-AU 15 51735252 51735252 single base substitution G A downstream_gene_variant MELA-AU 15 51735283 51735283 single base substitution G A downstream_gene_variant MELA-AU 15 51735925 51735925 single base substitution A C downstream_gene_variant MELA-AU 15 51735946 51735946 single base substitution G A downstream_gene_variant MELA-AU 15 51736064 51736064 single base substitution G A downstream_gene_variant MELA-AU 15 51736074 51736074 single base substitution G A downstream_gene_variant MELA-AU 15 51736147 51736147 single base substitution G A downstream_gene_variant MELA-AU 15 51736316 51736316 single base substitution G A downstream_gene_variant MELA-AU 15 51737456 51737456 single base substitution C T downstream_gene_variant MELA-AU 15 51737793 51737793 single base substitution C T downstream_gene_variant MELA-AU 15 51738431 51738431 single base substitution G A downstream_gene_variant MELA-AU 15 51738593 51738593 single base substitution G A downstream_gene_variant MELA-AU 15 51738632 51738632 single base substitution T C downstream_gene_variant MELA-AU 15 51738696 51738696 single base substitution G A downstream_gene_variant MELA-AU 15 51738865 51738865 single base substitution C T downstream_gene_variant MELA-AU 15 51738929 51738929 single base substitution G A downstream_gene_variant MELA-AU 15 51739337 51739337 single base substitution C A downstream_gene_variant MELA-AU 15 51739503 51739503 single base substitution G A downstream_gene_variant MELA-AU 15 51739624 51739624 single base substitution C T downstream_gene_variant MELA-AU 15 51739733 51739733 single base substitution C T downstream_gene_variant MELA-AU 15 51739871 51739871 single base substitution C T downstream_gene_variant MELA-AU 15 51740149 51740149 single base substitution A G 3_prime_UTR_variant MELA-AU 15 51740149 51740149 single base substitution A G downstream_gene_variant MELA-AU 15 51740149 51740149 single base substitution A G exon_variant MELA-AU 15 51740340 51740340 single base substitution T A 3_prime_UTR_variant MELA-AU 15 51740340 51740340 single base substitution T A downstream_gene_variant MELA-AU 15 51740340 51740340 single base substitution T A exon_variant MELA-AU 15 51740343 51740355 deletion of <=200bp ATTTTAATTATGA - 3_prime_UTR_variant MELA-AU 15 51740343 51740355 deletion of <=200bp ATTTTAATTATGA - downstream_gene_variant MELA-AU 15 51740343 51740355 deletion of <=200bp ATTTTAATTATGA - exon_variant MELA-AU 15 51740424 51740424 single base substitution G A 3_prime_UTR_variant MELA-AU 15 51740424 51740424 single base substitution G A downstream_gene_variant MELA-AU 15 51740424 51740424 single base substitution G A exon_variant MELA-AU 15 51740639 51740639 single base substitution G A 3_prime_UTR_variant MELA-AU 15 51740639 51740639 single base substitution G A downstream_gene_variant MELA-AU 15 51740639 51740639 single base substitution G A exon_variant MELA-AU 15 51740663 51740663 single base substitution G A 3_prime_UTR_variant MELA-AU 15 51740663 51740663 single base substitution G A downstream_gene_variant MELA-AU 15 51740663 51740663 single base substitution G A exon_variant MELA-AU 15 51741558 51741558 single base substitution G A downstream_gene_variant MELA-AU 15 51741558 51741558 single base substitution G A intron_variant MELA-AU 15 51741616 51741616 single base substitution A G downstream_gene_variant MELA-AU 15 51741616 51741616 single base substitution A G intron_variant MELA-AU 15 51741993 51741993 single base substitution G A downstream_gene_variant MELA-AU 15 51741993 51741993 single base substitution G A intron_variant MELA-AU 15 51743801 51743801 single base substitution C T downstream_gene_variant MELA-AU 15 51743801 51743801 single base substitution C T intron_variant MELA-AU 15 51743801 51743801 single base substitution C T upstream_gene_variant MELA-AU 15 51744139 51744139 single base substitution G A downstream_gene_variant MELA-AU 15 51744139 51744139 single base substitution G A intron_variant MELA-AU 15 51744139 51744139 single base substitution G A upstream_gene_variant MELA-AU 15 51744596 51744596 single base substitution G T downstream_gene_variant MELA-AU 15 51744596 51744596 single base substitution G T intron_variant MELA-AU 15 51744596 51744596 single base substitution G T upstream_gene_variant MELA-AU 15 51744651 51744651 single base substitution T C downstream_gene_variant MELA-AU 15 51744651 51744651 single base substitution T C intron_variant MELA-AU 15 51744651 51744651 single base substitution T C upstream_gene_variant MELA-AU 15 51744739 51744739 single base substitution G A downstream_gene_variant MELA-AU 15 51744739 51744739 single base substitution G A intron_variant MELA-AU 15 51744739 51744739 single base substitution G A upstream_gene_variant MELA-AU 15 51745036 51745036 single base substitution A G downstream_gene_variant MELA-AU 15 51745036 51745036 single base substitution A G intron_variant MELA-AU 15 51745036 51745036 single base substitution A G upstream_gene_variant MELA-AU 15 51745266 51745266 single base substitution G A downstream_gene_variant MELA-AU 15 51745266 51745266 single base substitution G A intron_variant MELA-AU 15 51745266 51745266 single base substitution G A upstream_gene_variant MELA-AU 15 51745454 51745454 single base substitution G A downstream_gene_variant MELA-AU 15 51745454 51745454 single base substitution G A exon_variant MELA-AU 15 51745454 51745454 single base substitution G A intron_variant MELA-AU 15 51745454 51745454 single base substitution G A upstream_gene_variant MELA-AU 15 51746084 51746084 single base substitution C T downstream_gene_variant MELA-AU 15 51746084 51746084 single base substitution C T intron_variant MELA-AU 15 51746084 51746084 single base substitution C T upstream_gene_variant MELA-AU 15 51746690 51746690 single base substitution G A downstream_gene_variant MELA-AU 15 51746690 51746690 single base substitution G A intron_variant MELA-AU 15 51746690 51746690 single base substitution G A upstream_gene_variant MELA-AU 15 51746828 51746829 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 51746828 51746829 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51746828 51746829 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 51746839 51746839 single base substitution A C downstream_gene_variant MELA-AU 15 51746839 51746839 single base substitution A C intron_variant MELA-AU 15 51746839 51746839 single base substitution A C upstream_gene_variant MELA-AU 15 51746882 51746882 single base substitution G A downstream_gene_variant MELA-AU 15 51746882 51746882 single base substitution G A intron_variant MELA-AU 15 51746882 51746882 single base substitution G A upstream_gene_variant MELA-AU 15 51747160 51747160 single base substitution G A downstream_gene_variant MELA-AU 15 51747160 51747160 single base substitution G A intron_variant MELA-AU 15 51747160 51747160 single base substitution G A upstream_gene_variant MELA-AU 15 51747327 51747327 single base substitution G A downstream_gene_variant MELA-AU 15 51747327 51747327 single base substitution G A intron_variant MELA-AU 15 51747327 51747327 single base substitution G A upstream_gene_variant MELA-AU 15 51747493 51747493 single base substitution G A downstream_gene_variant MELA-AU 15 51747493 51747493 single base substitution G A intron_variant MELA-AU 15 51747493 51747493 single base substitution G A upstream_gene_variant MELA-AU 15 51747947 51747947 single base substitution G A downstream_gene_variant MELA-AU 15 51747947 51747947 single base substitution G A intron_variant MELA-AU 15 51747947 51747947 single base substitution G A upstream_gene_variant MELA-AU 15 51748348 51748348 single base substitution C T downstream_gene_variant MELA-AU 15 51748348 51748348 single base substitution C T exon_variant MELA-AU 15 51748348 51748348 single base substitution C T stop_gained W2156* 6467G>A MELA-AU 15 51748348 51748348 single base substitution C T stop_gained W2792* 8375G>A MELA-AU 15 51748348 51748348 single base substitution C T stop_gained W2793* 8378G>A MELA-AU 15 51748348 51748348 single base substitution C T stop_gained W938* 2813G>A MELA-AU 15 51748348 51748348 single base substitution C T upstream_gene_variant MELA-AU 15 51748622 51748622 single base substitution G A downstream_gene_variant MELA-AU 15 51748622 51748622 single base substitution G A intron_variant MELA-AU 15 51748622 51748622 single base substitution G A upstream_gene_variant MELA-AU 15 51748816 51748816 single base substitution C T downstream_gene_variant MELA-AU 15 51748816 51748816 single base substitution C T intron_variant MELA-AU 15 51748816 51748816 single base substitution C T upstream_gene_variant MELA-AU 15 51749005 51749005 single base substitution G A downstream_gene_variant MELA-AU 15 51749005 51749005 single base substitution G A intron_variant MELA-AU 15 51749005 51749005 single base substitution G A upstream_gene_variant MELA-AU 15 51749339 51749339 single base substitution A T downstream_gene_variant MELA-AU 15 51749339 51749339 single base substitution A T intron_variant MELA-AU 15 51749339 51749339 single base substitution A T upstream_gene_variant MELA-AU 15 51749988 51749988 single base substitution G A intron_variant MELA-AU 15 51749988 51749988 single base substitution G A upstream_gene_variant MELA-AU 15 51750132 51750132 single base substitution G A intron_variant MELA-AU 15 51750132 51750132 single base substitution G A upstream_gene_variant MELA-AU 15 51750329 51750329 single base substitution G A downstream_gene_variant MELA-AU 15 51750329 51750329 single base substitution G A intron_variant MELA-AU 15 51750329 51750329 single base substitution G A upstream_gene_variant MELA-AU 15 51750475 51750475 single base substitution G A downstream_gene_variant MELA-AU 15 51750475 51750475 single base substitution G A intron_variant MELA-AU 15 51750475 51750475 single base substitution G A upstream_gene_variant MELA-AU 15 51750787 51750787 single base substitution T C 3_prime_UTR_variant MELA-AU 15 51750787 51750787 single base substitution T C downstream_gene_variant MELA-AU 15 51750787 51750787 single base substitution T C exon_variant MELA-AU 15 51750787 51750787 single base substitution T C missense_variant D2047G 6140A>G MELA-AU 15 51750787 51750787 single base substitution T C missense_variant D2683G 8048A>G MELA-AU 15 51750787 51750787 single base substitution T C missense_variant D2684G 8051A>G MELA-AU 15 51750787 51750787 single base substitution T C missense_variant D829G 2486A>G MELA-AU 15 51750787 51750787 single base substitution T C upstream_gene_variant MELA-AU 15 51751076 51751076 single base substitution G A downstream_gene_variant MELA-AU 15 51751076 51751076 single base substitution G A exon_variant MELA-AU 15 51751076 51751076 single base substitution G A intron_variant MELA-AU 15 51751076 51751076 single base substitution G A upstream_gene_variant MELA-AU 15 51751149 51751149 single base substitution G A downstream_gene_variant MELA-AU 15 51751149 51751149 single base substitution G A exon_variant MELA-AU 15 51751149 51751149 single base substitution G A intron_variant MELA-AU 15 51751149 51751149 single base substitution G A upstream_gene_variant MELA-AU 15 51751546 51751546 single base substitution C T downstream_gene_variant MELA-AU 15 51751546 51751546 single base substitution C T intron_variant MELA-AU 15 51751546 51751546 single base substitution C T upstream_gene_variant MELA-AU 15 51751687 51751687 single base substitution T C downstream_gene_variant MELA-AU 15 51751687 51751687 single base substitution T C intron_variant MELA-AU 15 51751687 51751687 single base substitution T C upstream_gene_variant MELA-AU 15 51751762 51751762 single base substitution G A downstream_gene_variant MELA-AU 15 51751762 51751762 single base substitution G A intron_variant MELA-AU 15 51751762 51751762 single base substitution G A upstream_gene_variant MELA-AU 15 51751904 51751904 single base substitution G A downstream_gene_variant MELA-AU 15 51751904 51751904 single base substitution G A exon_variant MELA-AU 15 51751904 51751904 single base substitution G A intron_variant MELA-AU 15 51751904 51751904 single base substitution G A upstream_gene_variant MELA-AU 15 51751960 51751960 single base substitution G A downstream_gene_variant MELA-AU 15 51751960 51751960 single base substitution G A exon_variant MELA-AU 15 51751960 51751960 single base substitution G A intron_variant MELA-AU 15 51751960 51751960 single base substitution G A upstream_gene_variant MELA-AU 15 51752008 51752008 single base substitution A T downstream_gene_variant MELA-AU 15 51752008 51752008 single base substitution A T intron_variant MELA-AU 15 51752008 51752008 single base substitution A T upstream_gene_variant MELA-AU 15 51752300 51752301 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 51752300 51752301 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51752300 51752301 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 51752972 51752972 single base substitution G A downstream_gene_variant MELA-AU 15 51752972 51752972 single base substitution G A intron_variant MELA-AU 15 51752972 51752972 single base substitution G A upstream_gene_variant MELA-AU 15 51753527 51753527 single base substitution G A downstream_gene_variant MELA-AU 15 51753527 51753527 single base substitution G A intron_variant MELA-AU 15 51753527 51753527 single base substitution G A upstream_gene_variant MELA-AU 15 51753535 51753535 single base substitution G A downstream_gene_variant MELA-AU 15 51753535 51753535 single base substitution G A intron_variant MELA-AU 15 51753535 51753535 single base substitution G A upstream_gene_variant MELA-AU 15 51753787 51753787 single base substitution C T downstream_gene_variant MELA-AU 15 51753787 51753787 single base substitution C T intron_variant MELA-AU 15 51753787 51753787 single base substitution C T upstream_gene_variant MELA-AU 15 51754237 51754237 single base substitution G A downstream_gene_variant MELA-AU 15 51754237 51754237 single base substitution G A intron_variant MELA-AU 15 51754237 51754237 single base substitution G A upstream_gene_variant MELA-AU 15 51754367 51754367 single base substitution G A downstream_gene_variant MELA-AU 15 51754367 51754367 single base substitution G A intron_variant MELA-AU 15 51754367 51754367 single base substitution G A upstream_gene_variant MELA-AU 15 51754446 51754446 single base substitution G A downstream_gene_variant MELA-AU 15 51754446 51754446 single base substitution G A intron_variant MELA-AU 15 51754446 51754446 single base substitution G A upstream_gene_variant MELA-AU 15 51754726 51754726 single base substitution G A downstream_gene_variant MELA-AU 15 51754726 51754726 single base substitution G A intron_variant MELA-AU 15 51754726 51754726 single base substitution G A upstream_gene_variant MELA-AU 15 51754772 51754772 single base substitution G A downstream_gene_variant MELA-AU 15 51754772 51754772 single base substitution G A intron_variant MELA-AU 15 51754772 51754772 single base substitution G A upstream_gene_variant MELA-AU 15 51754803 51754803 single base substitution G A downstream_gene_variant MELA-AU 15 51754803 51754803 single base substitution G A intron_variant MELA-AU 15 51754803 51754803 single base substitution G A upstream_gene_variant MELA-AU 15 51754930 51754930 single base substitution G A downstream_gene_variant MELA-AU 15 51754930 51754930 single base substitution G A intron_variant MELA-AU 15 51754930 51754930 single base substitution G A upstream_gene_variant MELA-AU 15 51754951 51754952 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 51754951 51754952 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51754951 51754952 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 51755671 51755671 single base substitution G A exon_variant MELA-AU 15 51755671 51755671 single base substitution G A intron_variant MELA-AU 15 51755671 51755671 single base substitution G A missense_variant P1974S 5920C>T MELA-AU 15 51755671 51755671 single base substitution G A missense_variant P2610S 7828C>T MELA-AU 15 51755671 51755671 single base substitution G A missense_variant P2611S 7831C>T MELA-AU 15 51755671 51755671 single base substitution G A missense_variant P735S 2203C>T MELA-AU 15 51755671 51755671 single base substitution G A upstream_gene_variant MELA-AU 15 51755672 51755672 single base substitution A G exon_variant MELA-AU 15 51755672 51755672 single base substitution A G intron_variant MELA-AU 15 51755672 51755672 single base substitution A G synonymous_variant F1973F 5919T>C MELA-AU 15 51755672 51755672 single base substitution A G synonymous_variant F2609F 7827T>C MELA-AU 15 51755672 51755672 single base substitution A G synonymous_variant F2610F 7830T>C MELA-AU 15 51755672 51755672 single base substitution A G synonymous_variant F734F 2202T>C MELA-AU 15 51755672 51755672 single base substitution A G upstream_gene_variant MELA-AU 15 51756171 51756171 single base substitution A T intron_variant MELA-AU 15 51756171 51756171 single base substitution A T upstream_gene_variant MELA-AU 15 51756706 51756706 single base substitution A T intron_variant MELA-AU 15 51756706 51756706 single base substitution A T upstream_gene_variant MELA-AU 15 51756911 51756911 single base substitution C T exon_variant MELA-AU 15 51756911 51756911 single base substitution C T intron_variant MELA-AU 15 51756911 51756911 single base substitution C T missense_variant R1953Q 5858G>A MELA-AU 15 51756911 51756911 single base substitution C T missense_variant R2589Q 7766G>A MELA-AU 15 51756911 51756911 single base substitution C T missense_variant R2590Q 7769G>A MELA-AU 15 51756911 51756911 single base substitution C T missense_variant R714Q 2141G>A MELA-AU 15 51756911 51756911 single base substitution C T upstream_gene_variant MELA-AU 15 51756950 51756950 single base substitution G A exon_variant MELA-AU 15 51756950 51756950 single base substitution G A intron_variant MELA-AU 15 51756950 51756950 single base substitution G A missense_variant P1940L 5819C>T MELA-AU 15 51756950 51756950 single base substitution G A missense_variant P2576L 7727C>T MELA-AU 15 51756950 51756950 single base substitution G A missense_variant P2577L 7730C>T MELA-AU 15 51756950 51756950 single base substitution G A missense_variant P701L 2102C>T MELA-AU 15 51756950 51756950 single base substitution G A upstream_gene_variant MELA-AU 15 51756990 51756990 single base substitution G A exon_variant MELA-AU 15 51756990 51756990 single base substitution G A intron_variant MELA-AU 15 51756990 51756990 single base substitution G A stop_gained Q1927* 5779C>T MELA-AU 15 51756990 51756990 single base substitution G A stop_gained Q2563* 7687C>T MELA-AU 15 51756990 51756990 single base substitution G A stop_gained Q2564* 7690C>T MELA-AU 15 51756990 51756990 single base substitution G A stop_gained Q688* 2062C>T MELA-AU 15 51757118 51757118 single base substitution G A intron_variant MELA-AU 15 51757353 51757353 single base substitution G A intron_variant MELA-AU 15 51757879 51757879 single base substitution A C intron_variant MELA-AU 15 51758365 51758365 single base substitution G A intron_variant MELA-AU 15 51759620 51759620 single base substitution G A intron_variant MELA-AU 15 51759626 51759626 single base substitution G A intron_variant MELA-AU 15 51759783 51759783 single base substitution G A intron_variant MELA-AU 15 51760480 51760480 single base substitution G A intron_variant MELA-AU 15 51760622 51760622 single base substitution A G intron_variant MELA-AU 15 51760733 51760733 single base substitution C T intron_variant MELA-AU 15 51760980 51760980 single base substitution G A intron_variant MELA-AU 15 51761178 51761178 single base substitution G A intron_variant MELA-AU 15 51762099 51762099 single base substitution G A intron_variant MELA-AU 15 51762169 51762169 single base substitution G A intron_variant MELA-AU 15 51762281 51762281 single base substitution G A intron_variant MELA-AU 15 51762763 51762764 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51764080 51764080 single base substitution G A intron_variant MELA-AU 15 51764080 51764080 single base substitution G A upstream_gene_variant MELA-AU 15 51764143 51764143 single base substitution G A intron_variant MELA-AU 15 51764143 51764143 single base substitution G A upstream_gene_variant MELA-AU 15 51764206 51764206 single base substitution G A intron_variant MELA-AU 15 51764206 51764206 single base substitution G A upstream_gene_variant MELA-AU 15 51764236 51764236 single base substitution G A intron_variant MELA-AU 15 51764236 51764236 single base substitution G A upstream_gene_variant MELA-AU 15 51764331 51764331 single base substitution G A intron_variant MELA-AU 15 51764331 51764331 single base substitution G A upstream_gene_variant MELA-AU 15 51764792 51764792 single base substitution G A intron_variant MELA-AU 15 51764792 51764792 single base substitution G A upstream_gene_variant MELA-AU 15 51765149 51765150 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51765149 51765150 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 51765191 51765191 single base substitution A T intron_variant MELA-AU 15 51765191 51765191 single base substitution A T upstream_gene_variant MELA-AU 15 51765397 51765397 single base substitution C A intron_variant MELA-AU 15 51765397 51765397 single base substitution C A upstream_gene_variant MELA-AU 15 51765870 51765870 single base substitution A T intron_variant MELA-AU 15 51765870 51765870 single base substitution A T upstream_gene_variant MELA-AU 15 51765947 51765947 single base substitution G A intron_variant MELA-AU 15 51765947 51765947 single base substitution G A upstream_gene_variant MELA-AU 15 51765989 51765989 single base substitution G A intron_variant MELA-AU 15 51765989 51765989 single base substitution G A upstream_gene_variant MELA-AU 15 51766572 51766572 single base substitution C T synonymous_variant V1757V 5271G>A MELA-AU 15 51766572 51766572 single base substitution C T synonymous_variant V2393V 7179G>A MELA-AU 15 51766572 51766572 single base substitution C T synonymous_variant V2394V 7182G>A MELA-AU 15 51766572 51766572 single base substitution C T synonymous_variant V518V 1554G>A MELA-AU 15 51766572 51766572 single base substitution C T upstream_gene_variant MELA-AU 15 51766719 51766719 single base substitution T A synonymous_variant L1708L 5124A>T MELA-AU 15 51766719 51766719 single base substitution T A synonymous_variant L2344L 7032A>T MELA-AU 15 51766719 51766719 single base substitution T A synonymous_variant L2345L 7035A>T MELA-AU 15 51766719 51766719 single base substitution T A synonymous_variant L469L 1407A>T MELA-AU 15 51766719 51766719 single base substitution T A upstream_gene_variant MELA-AU 15 51766853 51766853 single base substitution C T intron_variant MELA-AU 15 51766853 51766853 single base substitution C T upstream_gene_variant MELA-AU 15 51767216 51767216 single base substitution G A intron_variant MELA-AU 15 51767216 51767216 single base substitution G A upstream_gene_variant MELA-AU 15 51768159 51768159 single base substitution G A intron_variant MELA-AU 15 51768159 51768159 single base substitution G A upstream_gene_variant MELA-AU 15 51768324 51768324 single base substitution G A intron_variant MELA-AU 15 51768324 51768324 single base substitution G A upstream_gene_variant MELA-AU 15 51768681 51768681 single base substitution G A intron_variant MELA-AU 15 51769033 51769033 single base substitution C T intron_variant MELA-AU 15 51769578 51769578 single base substitution T A intron_variant MELA-AU 15 51769785 51769785 single base substitution G A intron_variant MELA-AU 15 51770065 51770065 single base substitution G A intron_variant MELA-AU 15 51770159 51770159 single base substitution G A intron_variant MELA-AU 15 51770189 51770189 single base substitution A G intron_variant MELA-AU 15 51770372 51770372 single base substitution G A intron_variant MELA-AU 15 51770389 51770389 single base substitution G A intron_variant MELA-AU 15 51770934 51770934 single base substitution G A intron_variant MELA-AU 15 51771037 51771037 single base substitution G A intron_variant MELA-AU 15 51771516 51771516 single base substitution G A intron_variant MELA-AU 15 51771517 51771517 single base substitution G A intron_variant MELA-AU 15 51771951 51771951 single base substitution G A intron_variant MELA-AU 15 51772060 51772060 single base substitution C T intron_variant MELA-AU 15 51772066 51772066 single base substitution A C intron_variant MELA-AU 15 51772523 51772523 single base substitution G A intron_variant MELA-AU 15 51772841 51772841 single base substitution G A synonymous_variant L1518L 4554C>T MELA-AU 15 51772841 51772841 single base substitution G A synonymous_variant L2154L 6462C>T MELA-AU 15 51772841 51772841 single base substitution G A synonymous_variant L278L 834C>T MELA-AU 15 51772969 51772969 single base substitution G A stop_gained Q1476* 4426C>T MELA-AU 15 51772969 51772969 single base substitution G A stop_gained Q2112* 6334C>T MELA-AU 15 51772969 51772969 single base substitution G A stop_gained Q236* 706C>T MELA-AU 15 51773217 51773217 single base substitution G A missense_variant P1393L 4178C>T MELA-AU 15 51773217 51773217 single base substitution G A missense_variant P153L 458C>T MELA-AU 15 51773217 51773217 single base substitution G A missense_variant P2029L 6086C>T MELA-AU 15 51773525 51773525 single base substitution G A synonymous_variant F1290F 3870C>T MELA-AU 15 51773525 51773525 single base substitution G A synonymous_variant F1926F 5778C>T MELA-AU 15 51773525 51773525 single base substitution G A synonymous_variant F50F 150C>T MELA-AU 15 51773642 51773642 single base substitution G A synonymous_variant T11T 33C>T MELA-AU 15 51773642 51773642 single base substitution G A synonymous_variant T1251T 3753C>T MELA-AU 15 51773642 51773642 single base substitution G A synonymous_variant T1887T 5661C>T MELA-AU 15 51773724 51773724 single base substitution C T missense_variant G1224E 3671G>A MELA-AU 15 51773724 51773724 single base substitution C T missense_variant G1860E 5579G>A MELA-AU 15 51773724 51773724 single base substitution C T upstream_gene_variant MELA-AU 15 51773794 51773795 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant VA1200VT MELA-AU 15 51773794 51773795 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant VA1836VT MELA-AU 15 51773794 51773795 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 51773937 51773937 single base substitution G A intron_variant MELA-AU 15 51773937 51773937 single base substitution G A upstream_gene_variant MELA-AU 15 51773975 51773975 single base substitution T A intron_variant MELA-AU 15 51773975 51773975 single base substitution T A upstream_gene_variant MELA-AU 15 51773998 51773998 single base substitution C T intron_variant MELA-AU 15 51773998 51773998 single base substitution C T upstream_gene_variant MELA-AU 15 51774012 51774012 single base substitution G A intron_variant MELA-AU 15 51774012 51774012 single base substitution G A upstream_gene_variant MELA-AU 15 51774668 51774668 single base substitution A G intron_variant MELA-AU 15 51774668 51774668 single base substitution A G upstream_gene_variant MELA-AU 15 51774686 51774686 single base substitution G A intron_variant MELA-AU 15 51774686 51774686 single base substitution G A upstream_gene_variant MELA-AU 15 51774946 51774946 single base substitution C T intron_variant MELA-AU 15 51774946 51774946 single base substitution C T upstream_gene_variant MELA-AU 15 51775100 51775100 single base substitution G A intron_variant MELA-AU 15 51775100 51775100 single base substitution G A upstream_gene_variant MELA-AU 15 51775109 51775109 single base substitution A G intron_variant MELA-AU 15 51775109 51775109 single base substitution A G upstream_gene_variant MELA-AU 15 51775253 51775253 single base substitution G A intron_variant MELA-AU 15 51775253 51775253 single base substitution G A upstream_gene_variant MELA-AU 15 51775889 51775889 single base substitution G A intron_variant MELA-AU 15 51775889 51775889 single base substitution G A upstream_gene_variant MELA-AU 15 51776334 51776334 single base substitution G A intron_variant MELA-AU 15 51776334 51776334 single base substitution G A upstream_gene_variant MELA-AU 15 51776439 51776439 single base substitution G A intron_variant MELA-AU 15 51776439 51776439 single base substitution G A upstream_gene_variant MELA-AU 15 51776607 51776624 deletion of <=200bp GCAAACTCTTTCAGCCTA - intron_variant MELA-AU 15 51776607 51776624 deletion of <=200bp GCAAACTCTTTCAGCCTA - upstream_gene_variant MELA-AU 15 51777182 51777182 single base substitution A C intron_variant MELA-AU 15 51777182 51777182 single base substitution A C upstream_gene_variant MELA-AU 15 51777213 51777213 single base substitution G A intron_variant MELA-AU 15 51777213 51777213 single base substitution G A upstream_gene_variant MELA-AU 15 51777355 51777355 single base substitution A T intron_variant MELA-AU 15 51777355 51777355 single base substitution A T upstream_gene_variant MELA-AU 15 51777360 51777360 single base substitution G A intron_variant MELA-AU 15 51777360 51777360 single base substitution G A upstream_gene_variant MELA-AU 15 51778007 51778007 single base substitution C T intron_variant MELA-AU 15 51778007 51778007 single base substitution C T upstream_gene_variant MELA-AU 15 51778014 51778014 single base substitution A T intron_variant MELA-AU 15 51778014 51778014 single base substitution A T upstream_gene_variant MELA-AU 15 51778234 51778234 single base substitution A G intron_variant MELA-AU 15 51778234 51778234 single base substitution A G upstream_gene_variant MELA-AU 15 51778249 51778249 single base substitution G A intron_variant MELA-AU 15 51778249 51778249 single base substitution G A upstream_gene_variant MELA-AU 15 51778443 51778443 single base substitution G A missense_variant S1134F 3401C>T MELA-AU 15 51778443 51778443 single base substitution G A missense_variant S1770F 5309C>T MELA-AU 15 51778443 51778443 single base substitution G A upstream_gene_variant MELA-AU 15 51778728 51778728 single base substitution C T intron_variant MELA-AU 15 51779172 51779172 single base substitution C T intron_variant MELA-AU 15 51779370 51779370 single base substitution G A intron_variant MELA-AU 15 51779516 51779516 single base substitution A C intron_variant MELA-AU 15 51779650 51779650 single base substitution G A intron_variant MELA-AU 15 51779689 51779689 single base substitution C T intron_variant MELA-AU 15 51779792 51779792 single base substitution C T intron_variant MELA-AU 15 51779981 51779981 single base substitution G A intron_variant MELA-AU 15 51780227 51780227 single base substitution G A missense_variant S1078F 3233C>T MELA-AU 15 51780227 51780227 single base substitution G A missense_variant S1714F 5141C>T MELA-AU 15 51780877 51780877 single base substitution G A intron_variant MELA-AU 15 51781259 51781259 single base substitution G A intron_variant MELA-AU 15 51781349 51781349 single base substitution C T intron_variant MELA-AU 15 51781994 51781994 single base substitution A T intron_variant MELA-AU 15 51782062 51782062 single base substitution G A intron_variant MELA-AU 15 51782470 51782470 single base substitution A G intron_variant MELA-AU 15 51782684 51782684 single base substitution G A intron_variant MELA-AU 15 51782948 51782948 single base substitution A C intron_variant MELA-AU 15 51783306 51783306 single base substitution A T intron_variant MELA-AU 15 51783311 51783311 single base substitution G A intron_variant MELA-AU 15 51783347 51783347 single base substitution A T intron_variant MELA-AU 15 51783546 51783546 single base substitution G A intron_variant MELA-AU 15 51783552 51783552 single base substitution C T intron_variant MELA-AU 15 51783644 51783644 single base substitution A G intron_variant MELA-AU 15 51783992 51783992 single base substitution G A intron_variant MELA-AU 15 51784150 51784150 single base substitution C T intron_variant MELA-AU 15 51784189 51784189 single base substitution A T intron_variant MELA-AU 15 51784195 51784195 single base substitution G A intron_variant MELA-AU 15 51784463 51784463 single base substitution C G intron_variant MELA-AU 15 51784578 51784578 single base substitution G A intron_variant MELA-AU 15 51785089 51785089 single base substitution T C intron_variant MELA-AU 15 51785308 51785308 single base substitution C T intron_variant MELA-AU 15 51785569 51785569 single base substitution C G intron_variant MELA-AU 15 51786062 51786062 single base substitution G A intron_variant MELA-AU 15 51786562 51786563 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 51786897 51786897 single base substitution C T intron_variant MELA-AU 15 51786920 51786920 single base substitution C T intron_variant MELA-AU 15 51787702 51787702 single base substitution G A intron_variant MELA-AU 15 51788220 51788220 single base substitution T A intron_variant MELA-AU 15 51788511 51788511 single base substitution G A intron_variant MELA-AU 15 51789496 51789496 single base substitution C T intron_variant MELA-AU 15 51790251 51790251 single base substitution G A intron_variant MELA-AU 15 51791932 51791932 single base substitution C T intron_variant MELA-AU 15 51791932 51791932 single base substitution C T synonymous_variant P1163P 3489G>A MELA-AU 15 51792321 51792321 single base substitution T C intron_variant MELA-AU 15 51792321 51792321 single base substitution T C missense_variant N1034D 3100A>G MELA-AU 15 51793402 51793402 single base substitution A G intron_variant MELA-AU 15 51793710 51793711 multiple base substitution (>=2bp and <=200bp) AT TA intron_variant MELA-AU 15 51793905 51793905 single base substitution C T intron_variant MELA-AU 15 51793980 51793980 single base substitution G A intron_variant MELA-AU 15 51794045 51794045 single base substitution A G intron_variant MELA-AU 15 51794822 51794822 single base substitution G A intron_variant MELA-AU 15 51795186 51795186 single base substitution G A intron_variant MELA-AU 15 51795186 51795186 single base substitution G A missense_variant P937S 2809C>T MELA-AU 15 51796141 51796141 single base substitution A T intron_variant MELA-AU 15 51796460 51796460 single base substitution C T intron_variant MELA-AU 15 51796788 51796788 single base substitution C T intron_variant MELA-AU 15 51797260 51797260 single base substitution A T intron_variant MELA-AU 15 51797625 51797625 single base substitution G A intron_variant MELA-AU 15 51798179 51798179 single base substitution C T intron_variant MELA-AU 15 51798280 51798280 single base substitution G A intron_variant MELA-AU 15 51798281 51798281 single base substitution G A intron_variant MELA-AU 15 51798566 51798566 single base substitution T C intron_variant MELA-AU 15 51799432 51799432 single base substitution A T missense_variant F888Y 2663T>A MELA-AU 15 51800467 51800467 single base substitution A G intron_variant MELA-AU 15 51800792 51800792 single base substitution T A intron_variant MELA-AU 15 51800939 51800939 single base substitution G A intron_variant MELA-AU 15 51801220 51801220 single base substitution G A intron_variant MELA-AU 15 51801644 51801644 single base substitution G A intron_variant MELA-AU 15 51801875 51801875 single base substitution A G intron_variant MELA-AU 15 51801993 51801993 single base substitution G A intron_variant MELA-AU 15 51802562 51802562 single base substitution G A intron_variant MELA-AU 15 51802753 51802753 single base substitution G A intron_variant MELA-AU 15 51802797 51802797 single base substitution G A intron_variant MELA-AU 15 51802860 51802860 single base substitution G C intron_variant MELA-AU 15 51803228 51803229 multiple base substitution (>=2bp and <=200bp) CA AC intron_variant MELA-AU 15 51803501 51803501 single base substitution G A intron_variant MELA-AU 15 51804011 51804011 single base substitution G A intron_variant MELA-AU 15 51804150 51804150 single base substitution A T intron_variant MELA-AU 15 51804566 51804566 single base substitution T A intron_variant MELA-AU 15 51804677 51804677 single base substitution G A intron_variant MELA-AU 15 51804701 51804701 single base substitution G A intron_variant MELA-AU 15 51804723 51804723 single base substitution G A intron_variant MELA-AU 15 51804953 51804953 single base substitution C T intron_variant MELA-AU 15 51805038 51805038 single base substitution G A intron_variant MELA-AU 15 51805768 51805768 single base substitution G A intron_variant MELA-AU 15 51805844 51805844 single base substitution G A intron_variant MELA-AU 15 51806017 51806017 single base substitution T A intron_variant MELA-AU 15 51806064 51806064 single base substitution G A intron_variant MELA-AU 15 51806152 51806152 single base substitution G A intron_variant MELA-AU 15 51806273 51806273 single base substitution G A intron_variant MELA-AU 15 51806553 51806553 single base substitution A G intron_variant MELA-AU 15 51807103 51807103 single base substitution G A intron_variant MELA-AU 15 51807479 51807479 single base substitution G A intron_variant MELA-AU 15 51807740 51807740 single base substitution T A intron_variant MELA-AU 15 51807834 51807834 single base substitution G A intron_variant MELA-AU 15 51808125 51808125 single base substitution G A intron_variant MELA-AU 15 51808278 51808278 single base substitution A T intron_variant MELA-AU 15 51808674 51808674 single base substitution G A intron_variant MELA-AU 15 51809244 51809244 single base substitution G A intron_variant MELA-AU 15 51809715 51809715 single base substitution G A intron_variant MELA-AU 15 51810057 51810057 single base substitution G A intron_variant MELA-AU 15 51810177 51810177 single base substitution G A intron_variant MELA-AU 15 51810318 51810318 single base substitution T A intron_variant MELA-AU 15 51810337 51810337 single base substitution C T intron_variant MELA-AU 15 51811103 51811103 single base substitution G A intron_variant MELA-AU 15 51811540 51811540 single base substitution C T intron_variant MELA-AU 15 51811947 51811947 single base substitution C T intron_variant MELA-AU 15 51812651 51812651 single base substitution G A intron_variant MELA-AU 15 51813029 51813029 single base substitution G A intron_variant MELA-AU 15 51813560 51813560 single base substitution A G intron_variant MELA-AU 15 51814193 51814193 single base substitution G A intron_variant MELA-AU 15 51814298 51814298 single base substitution G A intron_variant MELA-AU 15 51815316 51815316 single base substitution G A intron_variant MELA-AU 15 51815476 51815476 single base substitution G A intron_variant MELA-AU 15 51815492 51815492 single base substitution C T intron_variant MELA-AU 15 51815638 51815638 single base substitution G A intron_variant MELA-AU 15 51815729 51815729 single base substitution T A intron_variant MELA-AU 15 51816125 51816125 single base substitution G A intron_variant MELA-AU 15 51816127 51816127 single base substitution G A intron_variant MELA-AU 15 51816435 51816435 single base substitution G A intron_variant MELA-AU 15 51816601 51816601 single base substitution A G intron_variant MELA-AU 15 51816612 51816612 single base substitution G A intron_variant MELA-AU 15 51816741 51816741 single base substitution C T intron_variant MELA-AU 15 51817352 51817352 single base substitution G A intron_variant MELA-AU 15 51817371 51817371 single base substitution G A intron_variant MELA-AU 15 51817752 51817752 single base substitution G A intron_variant MELA-AU 15 51817815 51817815 single base substitution G A intron_variant MELA-AU 15 51817832 51817832 single base substitution G A intron_variant MELA-AU 15 51818390 51818390 single base substitution G A intron_variant MELA-AU 15 51818441 51818441 single base substitution G A intron_variant MELA-AU 15 51818777 51818777 single base substitution G A intron_variant MELA-AU 15 51818783 51818783 single base substitution G A intron_variant MELA-AU 15 51819138 51819138 single base substitution A C intron_variant MELA-AU 15 51819325 51819325 single base substitution G A intron_variant MELA-AU 15 51819814 51819814 single base substitution G A intron_variant MELA-AU 15 51819900 51819900 single base substitution A G intron_variant MELA-AU 15 51820033 51820033 single base substitution G A intron_variant MELA-AU 15 51820331 51820331 single base substitution A T intron_variant MELA-AU 15 51820559 51820559 single base substitution G A intron_variant MELA-AU 15 51820948 51820948 single base substitution T A intron_variant MELA-AU 15 51821009 51821009 single base substitution C T intron_variant MELA-AU 15 51821150 51821150 single base substitution G A intron_variant MELA-AU 15 51821469 51821469 deletion of <=200bp T - intron_variant MELA-AU 15 51821607 51821607 single base substitution G A intron_variant MELA-AU 15 51821709 51821709 single base substitution G A intron_variant MELA-AU 15 51821932 51821932 single base substitution G A intron_variant MELA-AU 15 51822185 51822185 single base substitution G A intron_variant MELA-AU 15 51822509 51822509 single base substitution G A intron_variant MELA-AU 15 51822645 51822645 single base substitution G A intron_variant MELA-AU 15 51822778 51822778 single base substitution C T intron_variant MELA-AU 15 51822957 51822957 single base substitution C T intron_variant MELA-AU 15 51823243 51823243 single base substitution G A intron_variant MELA-AU 15 51824236 51824236 single base substitution G A intron_variant MELA-AU 15 51824615 51824615 single base substitution T G intron_variant MELA-AU 15 51824751 51824751 single base substitution G A intron_variant MELA-AU 15 51824793 51824794 multiple base substitution (>=2bp and <=200bp) GA TT intron_variant MELA-AU 15 51825488 51825488 single base substitution G A intron_variant MELA-AU 15 51825732 51825732 single base substitution G A intron_variant MELA-AU 15 51825763 51825763 single base substitution G A intron_variant MELA-AU 15 51825897 51825897 single base substitution G A intron_variant MELA-AU 15 51825979 51825979 single base substitution G A intron_variant MELA-AU 15 51826350 51826350 single base substitution G A intron_variant MELA-AU 15 51826765 51826766 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51827475 51827475 single base substitution G A intron_variant MELA-AU 15 51828097 51828097 single base substitution C T intron_variant MELA-AU 15 51829383 51829383 single base substitution G A intron_variant MELA-AU 15 51829635 51829635 single base substitution C T intron_variant MELA-AU 15 51829950 51829950 single base substitution G A missense_variant S451F 1352C>T MELA-AU 15 51830352 51830352 single base substitution G A intron_variant MELA-AU 15 51830950 51830950 single base substitution T A intron_variant MELA-AU 15 51831199 51831199 single base substitution G A intron_variant MELA-AU 15 51831741 51831741 single base substitution C T intron_variant MELA-AU 15 51831818 51831818 single base substitution A C intron_variant MELA-AU 15 51832021 51832021 single base substitution C T intron_variant MELA-AU 15 51832370 51832370 single base substitution G A intron_variant MELA-AU 15 51832727 51832727 single base substitution G A intron_variant MELA-AU 15 51833046 51833046 single base substitution G A intron_variant MELA-AU 15 51833702 51833702 single base substitution G A intron_variant MELA-AU 15 51834479 51834479 single base substitution T A intron_variant MELA-AU 15 51834523 51834523 single base substitution C T splice_region_variant MELA-AU 15 51834661 51834661 single base substitution G A downstream_gene_variant MELA-AU 15 51834661 51834661 single base substitution G A missense_variant S325L 974C>T MELA-AU 15 51835568 51835568 single base substitution C T downstream_gene_variant MELA-AU 15 51835568 51835568 single base substitution C T intron_variant MELA-AU 15 51837077 51837077 single base substitution A T downstream_gene_variant MELA-AU 15 51837077 51837077 single base substitution A T intron_variant MELA-AU 15 51837081 51837081 single base substitution A T downstream_gene_variant MELA-AU 15 51837081 51837081 single base substitution A T intron_variant MELA-AU 15 51837253 51837253 single base substitution A T downstream_gene_variant MELA-AU 15 51837253 51837253 single base substitution A T intron_variant MELA-AU 15 51837919 51837919 single base substitution A T downstream_gene_variant MELA-AU 15 51837919 51837919 single base substitution A T missense_variant V264E 791T>A MELA-AU 15 51837989 51837989 single base substitution G A downstream_gene_variant MELA-AU 15 51837989 51837989 single base substitution G A intron_variant MELA-AU 15 51838015 51838015 single base substitution A C downstream_gene_variant MELA-AU 15 51838015 51838015 single base substitution A C intron_variant MELA-AU 15 51838199 51838199 single base substitution G A downstream_gene_variant MELA-AU 15 51838199 51838199 single base substitution G A intron_variant MELA-AU 15 51838404 51838404 single base substitution G A downstream_gene_variant MELA-AU 15 51838404 51838404 single base substitution G A intron_variant MELA-AU 15 51839031 51839031 single base substitution C T downstream_gene_variant MELA-AU 15 51839031 51839031 single base substitution C T intron_variant MELA-AU 15 51839457 51839457 single base substitution G A downstream_gene_variant MELA-AU 15 51839457 51839457 single base substitution G A missense_variant S239L 716C>T MELA-AU 15 51840044 51840044 single base substitution C T intron_variant MELA-AU 15 51840139 51840139 single base substitution T C intron_variant MELA-AU 15 51840153 51840153 single base substitution C T intron_variant MELA-AU 15 51840937 51840937 single base substitution A G intron_variant MELA-AU 15 51841015 51841015 single base substitution G A intron_variant MELA-AU 15 51841102 51841102 single base substitution G A intron_variant MELA-AU 15 51841103 51841103 single base substitution G A intron_variant MELA-AU 15 51841870 51841870 single base substitution C T intron_variant MELA-AU 15 51842307 51842307 single base substitution G A intron_variant MELA-AU 15 51842443 51842443 single base substitution C A intron_variant MELA-AU 15 51842823 51842823 single base substitution C G intron_variant MELA-AU 15 51842901 51842901 single base substitution G A intron_variant MELA-AU 15 51842932 51842932 single base substitution C T intron_variant MELA-AU 15 51843216 51843216 single base substitution G A intron_variant MELA-AU 15 51843377 51843377 single base substitution G A intron_variant MELA-AU 15 51844020 51844020 single base substitution G A intron_variant MELA-AU 15 51844450 51844451 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51844843 51844843 single base substitution C T intron_variant MELA-AU 15 51844890 51844890 single base substitution C T intron_variant MELA-AU 15 51845216 51845216 single base substitution C T intron_variant MELA-AU 15 51845351 51845351 single base substitution G A intron_variant MELA-AU 15 51846144 51846144 single base substitution G A intron_variant MELA-AU 15 51846248 51846248 single base substitution G A intron_variant MELA-AU 15 51846491 51846491 single base substitution C T intron_variant MELA-AU 15 51846648 51846648 single base substitution G A intron_variant MELA-AU 15 51847203 51847203 single base substitution A G intron_variant MELA-AU 15 51847588 51847589 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51848467 51848467 single base substitution G A intron_variant MELA-AU 15 51848992 51848992 single base substitution C T intron_variant MELA-AU 15 51849258 51849258 single base substitution G A intron_variant MELA-AU 15 51849294 51849294 single base substitution A G intron_variant MELA-AU 15 51849350 51849350 single base substitution G A intron_variant MELA-AU 15 51849693 51849693 single base substitution G A intron_variant MELA-AU 15 51850369 51850369 single base substitution A T intron_variant MELA-AU 15 51850483 51850483 single base substitution T C intron_variant MELA-AU 15 51851844 51851844 single base substitution G A intron_variant MELA-AU 15 51852617 51852617 single base substitution G A intron_variant MELA-AU 15 51853100 51853100 single base substitution T C intron_variant MELA-AU 15 51853583 51853583 single base substitution T C intron_variant MELA-AU 15 51854872 51854872 single base substitution A T downstream_gene_variant MELA-AU 15 51854872 51854872 single base substitution A T intron_variant MELA-AU 15 51855009 51855009 single base substitution G A downstream_gene_variant MELA-AU 15 51855009 51855009 single base substitution G A intron_variant MELA-AU 15 51855136 51855136 single base substitution G A downstream_gene_variant MELA-AU 15 51855136 51855136 single base substitution G A intron_variant MELA-AU 15 51855424 51855424 single base substitution G A downstream_gene_variant MELA-AU 15 51855424 51855424 single base substitution G A intron_variant MELA-AU 15 51855657 51855657 single base substitution G A downstream_gene_variant MELA-AU 15 51855657 51855657 single base substitution G A intron_variant MELA-AU 15 51855715 51855715 single base substitution G A downstream_gene_variant MELA-AU 15 51855715 51855715 single base substitution G A intron_variant MELA-AU 15 51856745 51856745 single base substitution G A downstream_gene_variant MELA-AU 15 51856745 51856745 single base substitution G A intron_variant MELA-AU 15 51857789 51857789 single base substitution G A downstream_gene_variant MELA-AU 15 51857789 51857789 single base substitution G A intron_variant MELA-AU 15 51857998 51857998 single base substitution C T downstream_gene_variant MELA-AU 15 51857998 51857998 single base substitution C T intron_variant MELA-AU 15 51858025 51858025 single base substitution G T downstream_gene_variant MELA-AU 15 51858025 51858025 single base substitution G T intron_variant MELA-AU 15 51858724 51858724 single base substitution G A downstream_gene_variant MELA-AU 15 51858724 51858724 single base substitution G A intron_variant MELA-AU 15 51859341 51859341 single base substitution G A exon_variant MELA-AU 15 51859341 51859341 single base substitution G A intron_variant MELA-AU 15 51859437 51859437 single base substitution A G exon_variant MELA-AU 15 51859437 51859437 single base substitution A G intron_variant MELA-AU 15 51859581 51859581 single base substitution A C exon_variant MELA-AU 15 51859581 51859581 single base substitution A C intron_variant MELA-AU 15 51859987 51859987 single base substitution G A exon_variant MELA-AU 15 51859987 51859987 single base substitution G A intron_variant MELA-AU 15 51860252 51860252 single base substitution G A exon_variant MELA-AU 15 51860252 51860252 single base substitution G A intron_variant MELA-AU 15 51860294 51860294 single base substitution G A exon_variant MELA-AU 15 51860294 51860294 single base substitution G A intron_variant MELA-AU 15 51860979 51860979 single base substitution T A intron_variant MELA-AU 15 51861319 51861319 single base substitution G A intron_variant MELA-AU 15 51861553 51861554 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 51861557 51861557 single base substitution G A intron_variant MELA-AU 15 51862247 51862248 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51862459 51862459 single base substitution G A intron_variant MELA-AU 15 51862537 51862537 single base substitution G A intron_variant MELA-AU 15 51862714 51862714 single base substitution G A intron_variant MELA-AU 15 51862871 51862871 single base substitution C T intron_variant MELA-AU 15 51864081 51864081 single base substitution A T intron_variant MELA-AU 15 51864155 51864155 single base substitution G A intron_variant MELA-AU 15 51864590 51864590 single base substitution C T intron_variant MELA-AU 15 51865182 51865182 single base substitution G A intron_variant MELA-AU 15 51865906 51865906 single base substitution G A intron_variant MELA-AU 15 51866738 51866738 single base substitution G A intron_variant MELA-AU 15 51866889 51866889 single base substitution G C intron_variant MELA-AU 15 51866926 51866926 single base substitution T C intron_variant MELA-AU 15 51867407 51867407 single base substitution A C intron_variant MELA-AU 15 51867411 51867411 single base substitution A G intron_variant MELA-AU 15 51868550 51868550 single base substitution A G intron_variant MELA-AU 15 51868689 51868689 single base substitution T G intron_variant MELA-AU 15 51871310 51871310 single base substitution G A intron_variant MELA-AU 15 51872550 51872550 single base substitution G A intron_variant MELA-AU 15 51872837 51872837 single base substitution G A intron_variant MELA-AU 15 51872935 51872935 single base substitution G A intron_variant MELA-AU 15 51873357 51873357 single base substitution G A intron_variant MELA-AU 15 51873691 51873691 single base substitution G A intron_variant MELA-AU 15 51873862 51873862 single base substitution C T intron_variant MELA-AU 15 51874775 51874775 single base substitution C T intron_variant MELA-AU 15 51875146 51875146 single base substitution C T intron_variant MELA-AU 15 51875148 51875148 single base substitution G A intron_variant MELA-AU 15 51877851 51877851 single base substitution G A intron_variant MELA-AU 15 51878163 51878163 single base substitution G A intron_variant MELA-AU 15 51878442 51878442 single base substitution G A intron_variant MELA-AU 15 51878543 51878543 single base substitution G C intron_variant MELA-AU 15 51878733 51878733 single base substitution A C intron_variant MELA-AU 15 51878926 51878926 single base substitution C T intron_variant MELA-AU 15 51879646 51879647 multiple base substitution (>=2bp and <=200bp) GA AC intron_variant MELA-AU 15 51880489 51880489 single base substitution G A intron_variant MELA-AU 15 51880628 51880628 single base substitution A G intron_variant MELA-AU 15 51880944 51880944 single base substitution C A intron_variant MELA-AU 15 51881246 51881246 single base substitution T G intron_variant MELA-AU 15 51881511 51881511 single base substitution G A intron_variant MELA-AU 15 51882036 51882036 single base substitution A T intron_variant MELA-AU 15 51882259 51882259 single base substitution G A intron_variant MELA-AU 15 51882439 51882439 single base substitution A G intron_variant MELA-AU 15 51882486 51882486 single base substitution G C intron_variant MELA-AU 15 51882724 51882724 single base substitution C T intron_variant MELA-AU 15 51882825 51882825 single base substitution G C intron_variant MELA-AU 15 51883018 51883018 single base substitution G A intron_variant MELA-AU 15 51883375 51883375 single base substitution C T intron_variant MELA-AU 15 51883692 51883692 single base substitution A C intron_variant MELA-AU 15 51884086 51884087 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 51884210 51884210 single base substitution C T intron_variant MELA-AU 15 51884222 51884222 single base substitution G A intron_variant MELA-AU 15 51884302 51884302 single base substitution A C intron_variant MELA-AU 15 51884323 51884323 single base substitution G A intron_variant MELA-AU 15 51884540 51884540 single base substitution G A intron_variant MELA-AU 15 51884755 51884755 single base substitution T A intron_variant MELA-AU 15 51884826 51884826 single base substitution G A intron_variant MELA-AU 15 51884838 51884838 single base substitution G A intron_variant MELA-AU 15 51884887 51884887 single base substitution G C intron_variant MELA-AU 15 51885480 51885480 single base substitution G A intron_variant MELA-AU 15 51885872 51885872 single base substitution C T intron_variant MELA-AU 15 51886322 51886322 single base substitution G A intron_variant MELA-AU 15 51886354 51886354 single base substitution G A intron_variant MELA-AU 15 51886687 51886687 single base substitution G A intron_variant MELA-AU 15 51889034 51889034 single base substitution C T intron_variant MELA-AU 15 51889057 51889057 single base substitution G A intron_variant MELA-AU 15 51889139 51889139 single base substitution G A intron_variant MELA-AU 15 51889609 51889609 single base substitution A C intron_variant MELA-AU 15 51890902 51890902 single base substitution G A intron_variant MELA-AU 15 51891069 51891069 single base substitution G A intron_variant MELA-AU 15 51891288 51891288 single base substitution T C intron_variant MELA-AU 15 51891393 51891393 single base substitution C T intron_variant MELA-AU 15 51891463 51891463 single base substitution C T intron_variant MELA-AU 15 51892089 51892089 single base substitution G A intron_variant MELA-AU 15 51892412 51892412 single base substitution C T intron_variant MELA-AU 15 51892609 51892609 single base substitution A G intron_variant MELA-AU 15 51892783 51892783 single base substitution G A intron_variant MELA-AU 15 51893407 51893407 single base substitution G A intron_variant MELA-AU 15 51893437 51893437 single base substitution G A intron_variant MELA-AU 15 51894197 51894197 single base substitution C T intron_variant MELA-AU 15 51894502 51894502 single base substitution G A intron_variant MELA-AU 15 51894503 51894503 single base substitution G A intron_variant MELA-AU 15 51894796 51894796 single base substitution C T intron_variant MELA-AU 15 51894806 51894806 single base substitution G A intron_variant MELA-AU 15 51894968 51894968 single base substitution G A intron_variant MELA-AU 15 51895234 51895235 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 51895384 51895384 single base substitution G A intron_variant MELA-AU 15 51895503 51895503 single base substitution G A intron_variant MELA-AU 15 51895635 51895635 single base substitution T A intron_variant MELA-AU 15 51895883 51895883 single base substitution G A exon_variant MELA-AU 15 51895883 51895883 single base substitution G A intron_variant MELA-AU 15 51895973 51895973 single base substitution G A intron_variant MELA-AU 15 51895973 51895973 single base substitution G A upstream_gene_variant MELA-AU 15 51896278 51896278 single base substitution G A intron_variant MELA-AU 15 51896278 51896278 single base substitution G A upstream_gene_variant MELA-AU 15 51896960 51896960 single base substitution G A intron_variant MELA-AU 15 51896960 51896960 single base substitution G A upstream_gene_variant MELA-AU 15 51898138 51898138 single base substitution A T intron_variant MELA-AU 15 51898138 51898138 single base substitution A T upstream_gene_variant MELA-AU 15 51898336 51898336 single base substitution A T intron_variant MELA-AU 15 51898336 51898336 single base substitution A T upstream_gene_variant MELA-AU 15 51898913 51898913 single base substitution G A intron_variant MELA-AU 15 51898913 51898913 single base substitution G A upstream_gene_variant MELA-AU 15 51898914 51898914 single base substitution G A intron_variant MELA-AU 15 51898914 51898914 single base substitution G A upstream_gene_variant MELA-AU 15 51899152 51899152 single base substitution C T intron_variant MELA-AU 15 51899152 51899152 single base substitution C T upstream_gene_variant MELA-AU 15 51899430 51899430 single base substitution G A intron_variant MELA-AU 15 51899430 51899430 single base substitution G A upstream_gene_variant MELA-AU 15 51900386 51900386 insertion of <=200bp - G intron_variant MELA-AU 15 51900386 51900386 insertion of <=200bp - G upstream_gene_variant MELA-AU 15 51900396 51900396 single base substitution G A intron_variant MELA-AU 15 51900396 51900396 single base substitution G A upstream_gene_variant MELA-AU 15 51901608 51901608 single base substitution G A intron_variant MELA-AU 15 51902670 51902670 single base substitution G A intron_variant MELA-AU 15 51903215 51903215 single base substitution C T intron_variant MELA-AU 15 51903284 51903284 single base substitution A C intron_variant MELA-AU 15 51903416 51903416 single base substitution C T intron_variant MELA-AU 15 51903790 51903790 single base substitution G A intron_variant MELA-AU 15 51904050 51904050 single base substitution G A intron_variant MELA-AU 15 51904052 51904052 single base substitution G A intron_variant MELA-AU 15 51904073 51904073 single base substitution C A intron_variant MELA-AU 15 51904305 51904305 single base substitution G A intron_variant MELA-AU 15 51904588 51904588 single base substitution G A intron_variant MELA-AU 15 51904753 51904753 single base substitution C T intron_variant MELA-AU 15 51905059 51905059 single base substitution C T intron_variant MELA-AU 15 51905121 51905121 single base substitution G A intron_variant MELA-AU 15 51905172 51905172 single base substitution G A intron_variant MELA-AU 15 51906986 51906986 single base substitution G A intron_variant MELA-AU 15 51907011 51907011 single base substitution G A intron_variant MELA-AU 15 51907304 51907304 single base substitution A T intron_variant MELA-AU 15 51907477 51907477 single base substitution G A intron_variant MELA-AU 15 51907826 51907826 single base substitution G A intron_variant MELA-AU 15 51908139 51908139 single base substitution A T intron_variant MELA-AU 15 51908346 51908346 single base substitution G A intron_variant MELA-AU 15 51908461 51908461 single base substitution G A intron_variant MELA-AU 15 51908521 51908521 single base substitution G A intron_variant MELA-AU 15 51908684 51908684 single base substitution C T intron_variant MELA-AU 15 51909463 51909463 single base substitution G A intron_variant MELA-AU 15 51909469 51909469 single base substitution G A intron_variant MELA-AU 15 51909511 51909511 single base substitution C T intron_variant MELA-AU 15 51911009 51911009 single base substitution A C intron_variant MELA-AU 15 51911177 51911177 single base substitution C A intron_variant MELA-AU 15 51911181 51911181 single base substitution A T intron_variant MELA-AU 15 51911436 51911436 single base substitution G A intron_variant MELA-AU 15 51911990 51911990 single base substitution T A intron_variant MELA-AU 15 51912058 51912058 single base substitution C G intron_variant MELA-AU 15 51912961 51912961 single base substitution G A intron_variant MELA-AU 15 51913012 51913016 deletion of <=200bp AAGTG - intron_variant MELA-AU 15 51915244 51915244 single base substitution C T upstream_gene_variant MELA-AU 15 51916109 51916109 single base substitution G A upstream_gene_variant MELA-AU 15 51916864 51916864 single base substitution G A upstream_gene_variant MELA-AU 15 51917274 51917274 single base substitution C T upstream_gene_variant MELA-AU 15 51918093 51918093 single base substitution G A upstream_gene_variant MELA-AU 15 51918104 51918104 single base substitution C T upstream_gene_variant MELA-AU 15 51918236 51918236 single base substitution C T upstream_gene_variant MELA-AU 15 51918287 51918287 single base substitution G A upstream_gene_variant MELA-AU 15 51918489 51918489 single base substitution C T upstream_gene_variant MELA-AU 15 51918507 51918507 single base substitution G A upstream_gene_variant MELA-AU 15 51919077 51919077 single base substitution G A upstream_gene_variant MELA-AU 15 51919519 51919519 deletion of <=200bp T - upstream_gene_variant MELA-AU 15 51919607 51919607 single base substitution G A upstream_gene_variant ORCA-IN 15 51744792 51744792 single base substitution A G downstream_gene_variant ORCA-IN 15 51744792 51744792 single base substitution A G intron_variant ORCA-IN 15 51744792 51744792 single base substitution A G upstream_gene_variant ORCA-IN 15 51756929 51756929 single base substitution G A exon_variant ORCA-IN 15 51756929 51756929 single base substitution G A intron_variant ORCA-IN 15 51756929 51756929 single base substitution G A missense_variant A1947V 5840C>T ORCA-IN 15 51756929 51756929 single base substitution G A missense_variant A2583V 7748C>T ORCA-IN 15 51756929 51756929 single base substitution G A missense_variant A2584V 7751C>T ORCA-IN 15 51756929 51756929 single base substitution G A missense_variant A708V 2123C>T ORCA-IN 15 51756929 51756929 single base substitution G A upstream_gene_variant ORCA-IN 15 51790939 51790939 single base substitution T A intron_variant ORCA-IN 15 51790939 51790939 single base substitution T A missense_variant K1494N 4482A>T ORCA-IN 15 51792650 51792650 single base substitution A C intron_variant ORCA-IN 15 51883171 51883171 single base substitution G C intron_variant ORCA-IN 15 51895785 51895785 single base substitution C T intron_variant OV-AU 15 51742443 51742443 single base substitution G A 3_prime_UTR_variant OV-AU 15 51742443 51742443 single base substitution G A downstream_gene_variant OV-AU 15 51742443 51742443 single base substitution G A exon_variant OV-AU 15 51742443 51742443 single base substitution G A synonymous_variant D1074D 3222C>T OV-AU 15 51742443 51742443 single base substitution G A synonymous_variant D2292D 6876C>T OV-AU 15 51742443 51742443 single base substitution G A synonymous_variant D2928D 8784C>T OV-AU 15 51742443 51742443 single base substitution G A synonymous_variant D2929D 8787C>T OV-AU 15 51753022 51753022 single base substitution C G downstream_gene_variant OV-AU 15 51753022 51753022 single base substitution C G intron_variant OV-AU 15 51753022 51753022 single base substitution C G upstream_gene_variant OV-AU 15 51761156 51761156 single base substitution A G intron_variant OV-AU 15 51772182 51772182 single base substitution A C missense_variant M1604R 4811T>G OV-AU 15 51772182 51772182 single base substitution A C missense_variant M2240R 6719T>G OV-AU 15 51772182 51772182 single base substitution A C missense_variant M364R 1091T>G OV-AU 15 51773225 51773225 single base substitution C A missense_variant E1390D 4170G>T OV-AU 15 51773225 51773225 single base substitution C A missense_variant E150D 450G>T OV-AU 15 51773225 51773225 single base substitution C A missense_variant E2026D 6078G>T OV-AU 15 51780803 51780803 single base substitution C T missense_variant D1029N 3085G>A OV-AU 15 51780803 51780803 single base substitution C T missense_variant D1665N 4993G>A OV-AU 15 51781527 51781527 single base substitution G C intron_variant OV-AU 15 51794217 51794217 single base substitution G A intron_variant OV-AU 15 51794252 51794252 single base substitution C A intron_variant OV-AU 15 51794270 51794270 single base substitution A G intron_variant OV-AU 15 51812249 51812249 single base substitution A C intron_variant OV-AU 15 51816314 51816314 single base substitution C A intron_variant OV-AU 15 51837678 51837678 single base substitution T C downstream_gene_variant OV-AU 15 51837678 51837678 single base substitution T C intron_variant OV-AU 15 51837719 51837719 single base substitution G A downstream_gene_variant OV-AU 15 51837719 51837719 single base substitution G A intron_variant OV-AU 15 51839126 51839126 single base substitution A G downstream_gene_variant OV-AU 15 51839126 51839126 single base substitution A G intron_variant OV-AU 15 51850752 51850752 single base substitution C T intron_variant OV-AU 15 51851142 51851142 single base substitution C T intron_variant OV-AU 15 51855295 51855295 single base substitution G C downstream_gene_variant OV-AU 15 51855295 51855295 single base substitution G C intron_variant OV-AU 15 51855818 51855818 single base substitution T G downstream_gene_variant OV-AU 15 51855818 51855818 single base substitution T G intron_variant OV-AU 15 51859248 51859248 single base substitution T C exon_variant OV-AU 15 51859248 51859248 single base substitution T C intron_variant OV-AU 15 51860117 51860117 single base substitution G A exon_variant OV-AU 15 51860117 51860117 single base substitution G A intron_variant OV-AU 15 51865255 51865255 single base substitution T A intron_variant OV-AU 15 51866004 51866004 single base substitution C T intron_variant OV-AU 15 51879082 51879082 single base substitution A C intron_variant OV-AU 15 51881985 51881985 single base substitution T C intron_variant OV-AU 15 51894277 51894277 single base substitution A G intron_variant OV-AU 15 51894381 51894381 single base substitution G T intron_variant OV-AU 15 51902123 51902123 single base substitution G C intron_variant OV-AU 15 51919727 51919727 single base substitution C T upstream_gene_variant OV-US 15 51795104 51795104 single base substitution A G intron_variant OV-US 15 51795104 51795104 single base substitution A G missense_variant L964P 2891T>C OV-US 15 51827951 51827951 single base substitution A G missense_variant F782S 2345T>C OV-US 15 51829847 51829847 single base substitution T G synonymous_variant P485P 1455A>C PACA-AU 15 51735446 51735446 single base substitution G A downstream_gene_variant PACA-AU 15 51745630 51745630 single base substitution A G downstream_gene_variant PACA-AU 15 51745630 51745630 single base substitution A G exon_variant PACA-AU 15 51745630 51745630 single base substitution A G intron_variant PACA-AU 15 51745630 51745630 single base substitution A G upstream_gene_variant PACA-AU 15 51751875 51751875 single base substitution G A downstream_gene_variant PACA-AU 15 51751875 51751875 single base substitution G A exon_variant PACA-AU 15 51751875 51751875 single base substitution G A intron_variant PACA-AU 15 51751875 51751875 single base substitution G A upstream_gene_variant PACA-AU 15 51752813 51752813 single base substitution G A downstream_gene_variant PACA-AU 15 51752813 51752813 single base substitution G A intron_variant PACA-AU 15 51752813 51752813 single base substitution G A upstream_gene_variant PACA-AU 15 51754746 51754746 single base substitution C G downstream_gene_variant PACA-AU 15 51754746 51754746 single base substitution C G intron_variant PACA-AU 15 51754746 51754746 single base substitution C G upstream_gene_variant PACA-AU 15 51760955 51760955 single base substitution G T intron_variant PACA-AU 15 51760980 51760980 single base substitution G A intron_variant PACA-AU 15 51772693 51772693 single base substitution G T intron_variant PACA-AU 15 51799444 51799444 single base substitution C T missense_variant R884H 2651G>A PACA-AU 15 51820710 51820710 single base substitution G A intron_variant PACA-AU 15 51822172 51822186 deletion of <=200bp CAACAGAATGAAGGA - intron_variant PACA-AU 15 51827984 51827984 single base substitution G A splice_region_variant PACA-AU 15 51837952 51837952 single base substitution C T downstream_gene_variant PACA-AU 15 51837952 51837952 single base substitution C T missense_variant C253Y 758G>A PACA-AU 15 51842809 51842809 deletion of <=200bp T - intron_variant PACA-AU 15 51846688 51846688 single base substitution T C intron_variant PACA-AU 15 51853738 51853738 single base substitution A T intron_variant PACA-AU 15 51856660 51856660 single base substitution A G downstream_gene_variant PACA-AU 15 51856660 51856660 single base substitution A G intron_variant PACA-AU 15 51864939 51864966 deletion of <=200bp ATGCTAAAAACTCTCAATAAACTAGGTA - intron_variant PACA-AU 15 51871635 51871635 single base substitution T G intron_variant PACA-AU 15 51873193 51873193 single base substitution G C intron_variant PACA-AU 15 51881550 51881550 single base substitution A G intron_variant PACA-AU 15 51886373 51886373 single base substitution T C intron_variant PACA-AU 15 51896595 51896595 single base substitution T A intron_variant PACA-AU 15 51896595 51896595 single base substitution T A upstream_gene_variant PACA-AU 15 51901130 51901130 single base substitution A G intron_variant PACA-AU 15 51908874 51908874 single base substitution C T intron_variant PACA-AU 15 51916863 51916863 single base substitution G A upstream_gene_variant PACA-AU 15 51919926 51919926 single base substitution A T upstream_gene_variant PACA-AU 15 51919927 51919927 single base substitution G T upstream_gene_variant PACA-AU 15 51919996 51919996 single base substitution C A upstream_gene_variant PACA-CA 15 51738466 51738466 single base substitution C T downstream_gene_variant PACA-CA 15 51740366 51740366 single base substitution T A 3_prime_UTR_variant PACA-CA 15 51740366 51740366 single base substitution T A downstream_gene_variant PACA-CA 15 51740366 51740366 single base substitution T A exon_variant PACA-CA 15 51742470 51742470 insertion of <=200bp - C downstream_gene_variant PACA-CA 15 51742470 51742470 insertion of <=200bp - C exon_variant PACA-CA 15 51742470 51742470 insertion of <=200bp - C frameshift_variant *77*? PACA-CA 15 51742470 51742470 insertion of <=200bp - C frameshift_variant G1065G? PACA-CA 15 51742470 51742470 insertion of <=200bp - C frameshift_variant G2283G? PACA-CA 15 51742470 51742470 insertion of <=200bp - C frameshift_variant G2919G? PACA-CA 15 51742470 51742470 insertion of <=200bp - C frameshift_variant G2920G? PACA-CA 15 51743295 51743295 single base substitution T C downstream_gene_variant PACA-CA 15 51743295 51743295 single base substitution T C intron_variant PACA-CA 15 51743295 51743295 single base substitution T C upstream_gene_variant PACA-CA 15 51746914 51746914 single base substitution G A downstream_gene_variant PACA-CA 15 51746914 51746914 single base substitution G A intron_variant PACA-CA 15 51746914 51746914 single base substitution G A upstream_gene_variant PACA-CA 15 51747076 51747076 insertion of <=200bp - A downstream_gene_variant PACA-CA 15 51747076 51747076 insertion of <=200bp - A intron_variant PACA-CA 15 51747076 51747076 insertion of <=200bp - A upstream_gene_variant PACA-CA 15 51752156 51752156 single base substitution T C downstream_gene_variant PACA-CA 15 51752156 51752156 single base substitution T C intron_variant PACA-CA 15 51752156 51752156 single base substitution T C upstream_gene_variant PACA-CA 15 51752221 51752221 single base substitution G C downstream_gene_variant PACA-CA 15 51752221 51752221 single base substitution G C intron_variant PACA-CA 15 51752221 51752221 single base substitution G C upstream_gene_variant PACA-CA 15 51755793 51755793 single base substitution G T intron_variant PACA-CA 15 51755793 51755793 single base substitution G T upstream_gene_variant PACA-CA 15 51767730 51767730 deletion of <=200bp A - intron_variant PACA-CA 15 51767730 51767730 deletion of <=200bp A - upstream_gene_variant PACA-CA 15 51770873 51770873 single base substitution A T intron_variant PACA-CA 15 51773234 51773234 single base substitution A G synonymous_variant P1387P 4161T>C PACA-CA 15 51773234 51773234 single base substitution A G synonymous_variant P147P 441T>C PACA-CA 15 51773234 51773234 single base substitution A G synonymous_variant P2023P 6069T>C PACA-CA 15 51774088 51774088 single base substitution C T intron_variant PACA-CA 15 51774088 51774088 single base substitution C T upstream_gene_variant PACA-CA 15 51775385 51775385 single base substitution G A intron_variant PACA-CA 15 51775385 51775385 single base substitution G A upstream_gene_variant PACA-CA 15 51775691 51775691 single base substitution G T intron_variant PACA-CA 15 51775691 51775691 single base substitution G T upstream_gene_variant PACA-CA 15 51775932 51775932 single base substitution C T intron_variant PACA-CA 15 51775932 51775932 single base substitution C T upstream_gene_variant PACA-CA 15 51777704 51777704 single base substitution T G intron_variant PACA-CA 15 51777704 51777704 single base substitution T G upstream_gene_variant PACA-CA 15 51778184 51778184 single base substitution G T intron_variant PACA-CA 15 51778184 51778184 single base substitution G T upstream_gene_variant PACA-CA 15 51779694 51779694 single base substitution G A intron_variant PACA-CA 15 51781007 51781007 single base substitution C A intron_variant PACA-CA 15 51782743 51782743 single base substitution G A intron_variant PACA-CA 15 51787394 51787394 single base substitution G T intron_variant PACA-CA 15 51795528 51795528 single base substitution C T intron_variant PACA-CA 15 51796483 51796483 single base substitution G A intron_variant PACA-CA 15 51801181 51801181 single base substitution C A intron_variant PACA-CA 15 51808385 51808385 single base substitution C G intron_variant PACA-CA 15 51810746 51810746 deletion of <=200bp A - intron_variant PACA-CA 15 51812905 51812905 single base substitution T G intron_variant PACA-CA 15 51815755 51815755 deletion of <=200bp A - intron_variant PACA-CA 15 51819787 51819787 single base substitution G A intron_variant PACA-CA 15 51828736 51828736 single base substitution G A synonymous_variant C647C 1941C>T PACA-CA 15 51829547 51829547 single base substitution A T intron_variant PACA-CA 15 51830521 51830521 single base substitution G A stop_gained R412* 1234C>T PACA-CA 15 51831485 51831485 single base substitution T G intron_variant PACA-CA 15 51831870 51831870 single base substitution G A intron_variant PACA-CA 15 51835650 51835650 single base substitution C T downstream_gene_variant PACA-CA 15 51835650 51835650 single base substitution C T intron_variant PACA-CA 15 51837511 51837511 single base substitution A G downstream_gene_variant PACA-CA 15 51837511 51837511 single base substitution A G intron_variant PACA-CA 15 51841913 51841913 single base substitution T C intron_variant PACA-CA 15 51849092 51849092 insertion of <=200bp - A intron_variant PACA-CA 15 51849560 51849560 single base substitution T C intron_variant PACA-CA 15 51849610 51849610 single base substitution C T intron_variant PACA-CA 15 51850066 51850066 single base substitution T G intron_variant PACA-CA 15 51858893 51858893 insertion of <=200bp - A downstream_gene_variant PACA-CA 15 51858893 51858893 insertion of <=200bp - A intron_variant PACA-CA 15 51870597 51870597 single base substitution T A intron_variant PACA-CA 15 51873381 51873381 single base substitution C T intron_variant PACA-CA 15 51873508 51873508 single base substitution C A intron_variant PACA-CA 15 51874478 51874478 single base substitution T C intron_variant PACA-CA 15 51875061 51875061 single base substitution C T intron_variant PACA-CA 15 51877897 51877897 single base substitution C T intron_variant PACA-CA 15 51880859 51880859 single base substitution C T intron_variant PACA-CA 15 51883306 51883306 single base substitution G A intron_variant PACA-CA 15 51884276 51884276 single base substitution G C intron_variant PACA-CA 15 51891220 51891220 single base substitution A G intron_variant PACA-CA 15 51898406 51898406 single base substitution T G intron_variant PACA-CA 15 51898406 51898406 single base substitution T G upstream_gene_variant PACA-CA 15 51901233 51901233 single base substitution A G intron_variant PACA-CA 15 51901837 51901837 single base substitution C T intron_variant PACA-CA 15 51906471 51906471 single base substitution A G intron_variant PACA-CA 15 51909460 51909460 single base substitution C T intron_variant PACA-CA 15 51911782 51911782 deletion of <=200bp A - intron_variant PACA-CA 15 51914730 51914730 single base substitution G A exon_variant PACA-CA 15 51914730 51914730 single base substitution G A stop_gained Q5* 13C>T PACA-CA 15 51916107 51916107 single base substitution A T upstream_gene_variant PACA-CA 15 51918343 51918343 single base substitution C T upstream_gene_variant PACA-CA 15 51919304 51919304 single base substitution G T upstream_gene_variant PAEN-AU 15 51745289 51745289 single base substitution T G downstream_gene_variant PAEN-AU 15 51745289 51745289 single base substitution T G intron_variant PAEN-AU 15 51745289 51745289 single base substitution T G upstream_gene_variant PAEN-AU 15 51769871 51769871 single base substitution G C intron_variant PAEN-AU 15 51785382 51785382 single base substitution C A intron_variant PAEN-AU 15 51831699 51831699 single base substitution G A intron_variant PAEN-IT 15 51743160 51743160 single base substitution C A downstream_gene_variant PAEN-IT 15 51743160 51743160 single base substitution C A intron_variant PAEN-IT 15 51743160 51743160 single base substitution C A upstream_gene_variant PAEN-IT 15 51750916 51750916 single base substitution G T 3_prime_UTR_variant PAEN-IT 15 51750916 51750916 single base substitution G T downstream_gene_variant PAEN-IT 15 51750916 51750916 single base substitution G T exon_variant PAEN-IT 15 51750916 51750916 single base substitution G T missense_variant S2031Y 6092C>A PAEN-IT 15 51750916 51750916 single base substitution G T missense_variant S2667Y 8000C>A PAEN-IT 15 51750916 51750916 single base substitution G T missense_variant S2668Y 8003C>A PAEN-IT 15 51750916 51750916 single base substitution G T missense_variant S813Y 2438C>A PAEN-IT 15 51750916 51750916 single base substitution G T upstream_gene_variant PAEN-IT 15 51813539 51813539 single base substitution G T intron_variant PAEN-IT 15 51870431 51870431 single base substitution G T intron_variant PAEN-IT 15 51887815 51887815 single base substitution C A intron_variant PBCA-DE 15 51766637 51766637 single base substitution C A missense_variant A1736S 5206G>T PBCA-DE 15 51766637 51766637 single base substitution C A missense_variant A2372S 7114G>T PBCA-DE 15 51766637 51766637 single base substitution C A missense_variant A2373S 7117G>T PBCA-DE 15 51766637 51766637 single base substitution C A missense_variant A497S 1489G>T PBCA-DE 15 51766637 51766637 single base substitution C A upstream_gene_variant PBCA-DE 15 51778089 51778089 single base substitution C T intron_variant PBCA-DE 15 51778089 51778089 single base substitution C T upstream_gene_variant PBCA-DE 15 51795362 51795362 single base substitution A G intron_variant PBCA-DE 15 51796204 51796204 single base substitution A C intron_variant PBCA-DE 15 51807013 51807013 single base substitution C T intron_variant PBCA-DE 15 51822731 51822731 insertion of <=200bp - CT intron_variant PBCA-DE 15 51829166 51829166 insertion of <=200bp - T intron_variant PBCA-DE 15 51832395 51832395 insertion of <=200bp - T intron_variant PBCA-DE 15 51835685 51835685 single base substitution T C downstream_gene_variant PBCA-DE 15 51835685 51835685 single base substitution T C intron_variant PBCA-DE 15 51836891 51836891 single base substitution A T downstream_gene_variant PBCA-DE 15 51836891 51836891 single base substitution A T intron_variant PBCA-DE 15 51844113 51844113 single base substitution T C intron_variant PBCA-DE 15 51851750 51851750 insertion of <=200bp - A intron_variant PBCA-DE 15 51856023 51856023 single base substitution C T downstream_gene_variant PBCA-DE 15 51856023 51856023 single base substitution C T intron_variant PBCA-DE 15 51872155 51872155 single base substitution C T intron_variant PBCA-DE 15 51872743 51872743 single base substitution C G intron_variant PBCA-DE 15 51875053 51875053 insertion of <=200bp - G intron_variant PBCA-DE 15 51899843 51899846 deletion of <=200bp CAAG - intron_variant PBCA-DE 15 51899843 51899846 deletion of <=200bp CAAG - upstream_gene_variant PBCA-DE 15 51902083 51902083 single base substitution C T intron_variant PBCA-DE 15 51911111 51911111 deletion of <=200bp G - intron_variant PRAD-CA 15 51738591 51738591 single base substitution G A downstream_gene_variant PRAD-CA 15 51768855 51768855 single base substitution G A missense_variant R1662C 4984C>T PRAD-CA 15 51768855 51768855 single base substitution G A missense_variant R2298C 6892C>T PRAD-CA 15 51768855 51768855 single base substitution G A missense_variant R2299C 6895C>T PRAD-CA 15 51768855 51768855 single base substitution G A missense_variant R423C 1267C>T PRAD-CA 15 51778176 51778176 single base substitution C A intron_variant PRAD-CA 15 51778176 51778176 single base substitution C A upstream_gene_variant PRAD-CA 15 51778360 51778360 single base substitution G A missense_variant R1162C 3484C>T PRAD-CA 15 51778360 51778360 single base substitution G A missense_variant R1798C 5392C>T PRAD-CA 15 51778360 51778360 single base substitution G A upstream_gene_variant PRAD-CA 15 51784494 51784494 single base substitution A T intron_variant PRAD-CA 15 51831713 51831713 single base substitution G A intron_variant PRAD-CA 15 51848552 51848552 single base substitution G A intron_variant PRAD-CA 15 51862687 51862687 single base substitution A T intron_variant PRAD-CA 15 51880759 51880759 single base substitution C T intron_variant PRAD-CA 15 51894449 51894449 single base substitution A C intron_variant PRAD-CA 15 51907504 51907504 single base substitution T C intron_variant PRAD-CA 15 51916010 51916010 single base substitution T C upstream_gene_variant PRAD-UK 15 51740125 51740125 single base substitution G A 3_prime_UTR_variant PRAD-UK 15 51740125 51740125 single base substitution G A downstream_gene_variant PRAD-UK 15 51740125 51740125 single base substitution G A exon_variant PRAD-UK 15 51778012 51778012 single base substitution T G intron_variant PRAD-UK 15 51778012 51778012 single base substitution T G upstream_gene_variant PRAD-UK 15 51797116 51797116 single base substitution G C intron_variant PRAD-UK 15 51852622 51852622 single base substitution A C intron_variant PRAD-UK 15 51864552 51864552 single base substitution T C intron_variant PRAD-UK 15 51903536 51903536 single base substitution T A intron_variant PRAD-UK 15 51914793 51914793 single base substitution G A 5_prime_UTR_variant PRAD-UK 15 51914793 51914793 single base substitution G A exon_variant PRAD-UK 15 51919035 51919035 single base substitution C T upstream_gene_variant PRAD-US 15 51750826 51750826 single base substitution T C downstream_gene_variant PRAD-US 15 51750826 51750826 single base substitution T C exon_variant PRAD-US 15 51750826 51750826 single base substitution T C splice_acceptor_variant PRAD-US 15 51750826 51750826 single base substitution T C upstream_gene_variant PRAD-US 15 51795002 51795002 single base substitution C T intron_variant PRAD-US 15 51795002 51795002 single base substitution C T splice_donor_variant PRAD-US 15 51855614 51855614 single base substitution C T downstream_gene_variant PRAD-US 15 51855614 51855614 single base substitution C T exon_variant PRAD-US 15 51855614 51855614 single base substitution C T stop_gained W177* 531G>A READ-US 15 51741273 51741273 single base substitution G T downstream_gene_variant READ-US 15 51741273 51741273 single base substitution G T exon_variant READ-US 15 51741273 51741273 single base substitution G T synonymous_variant R1153R 3457C>A READ-US 15 51741273 51741273 single base substitution G T synonymous_variant R2371R 7111C>A READ-US 15 51741273 51741273 single base substitution G T synonymous_variant R3007R 9019C>A READ-US 15 51741273 51741273 single base substitution G T synonymous_variant R3008R 9022C>A READ-US 15 51772220 51772220 single base substitution A C missense_variant N1591K 4773T>G READ-US 15 51772220 51772220 single base substitution A C missense_variant N2227K 6681T>G READ-US 15 51772220 51772220 single base substitution A C missense_variant N351K 1053T>G READ-US 15 51783791 51783791 single base substitution C T missense_variant R1010Q 3029G>A READ-US 15 51783791 51783791 single base substitution C T missense_variant R1646Q 4937G>A READ-US 15 51791854 51791854 single base substitution C T intron_variant READ-US 15 51791854 51791854 single base substitution C T synonymous_variant A1189A 3567G>A READ-US 15 51828428 51828428 single base substitution G T missense_variant S750Y 2249C>A READ-US 15 51829730 51829730 single base substitution C A synonymous_variant V524V 1572G>T READ-US 15 51839523 51839523 single base substitution C A downstream_gene_variant READ-US 15 51839523 51839523 single base substitution C A missense_variant R217M 650G>T READ-US 15 51860688 51860688 single base substitution T G exon_variant READ-US 15 51860688 51860688 single base substitution T G missense_variant N94T 281A>C RECA-EU 15 51743947 51743947 single base substitution G A downstream_gene_variant RECA-EU 15 51743947 51743947 single base substitution G A intron_variant RECA-EU 15 51743947 51743947 single base substitution G A upstream_gene_variant RECA-EU 15 51756063 51756063 single base substitution A T intron_variant RECA-EU 15 51756063 51756063 single base substitution A T upstream_gene_variant RECA-EU 15 51756683 51756683 single base substitution A G intron_variant RECA-EU 15 51756683 51756683 single base substitution A G upstream_gene_variant RECA-EU 15 51775734 51775734 single base substitution A G intron_variant RECA-EU 15 51775734 51775734 single base substitution A G upstream_gene_variant RECA-EU 15 51777405 51777405 single base substitution C A intron_variant RECA-EU 15 51777405 51777405 single base substitution C A upstream_gene_variant RECA-EU 15 51778155 51778155 single base substitution T A intron_variant RECA-EU 15 51778155 51778155 single base substitution T A upstream_gene_variant RECA-EU 15 51797194 51797194 single base substitution G T intron_variant RECA-EU 15 51809533 51809533 single base substitution G A intron_variant RECA-EU 15 51814857 51814857 single base substitution T A intron_variant RECA-EU 15 51817675 51817675 single base substitution C T intron_variant RECA-EU 15 51824220 51824220 single base substitution A T intron_variant RECA-EU 15 51824574 51824574 single base substitution C T intron_variant RECA-EU 15 51825707 51825707 single base substitution G A intron_variant RECA-EU 15 51827359 51827359 single base substitution A G intron_variant RECA-EU 15 51836785 51836785 single base substitution C T downstream_gene_variant RECA-EU 15 51836785 51836785 single base substitution C T intron_variant RECA-EU 15 51842459 51842459 single base substitution G A intron_variant RECA-EU 15 51847879 51847879 single base substitution C T intron_variant RECA-EU 15 51848913 51848913 single base substitution G A intron_variant RECA-EU 15 51869844 51869844 single base substitution G C intron_variant RECA-EU 15 51871121 51871121 single base substitution G A intron_variant RECA-EU 15 51880911 51880911 single base substitution T A intron_variant RECA-EU 15 51891700 51891700 single base substitution A T intron_variant RECA-EU 15 51897423 51897423 single base substitution C T intron_variant RECA-EU 15 51897423 51897423 single base substitution C T upstream_gene_variant RECA-EU 15 51897538 51897538 single base substitution C A intron_variant RECA-EU 15 51897538 51897538 single base substitution C A upstream_gene_variant RECA-EU 15 51900111 51900111 single base substitution C A intron_variant RECA-EU 15 51900111 51900111 single base substitution C A upstream_gene_variant RECA-EU 15 51910387 51910387 single base substitution G A intron_variant RECA-EU 15 51910388 51910388 single base substitution C T intron_variant SKCA-BR 15 51735788 51735788 single base substitution C T downstream_gene_variant SKCA-BR 15 51738703 51738703 single base substitution G A downstream_gene_variant SKCA-BR 15 51739119 51739119 single base substitution G A downstream_gene_variant SKCA-BR 15 51744528 51744528 single base substitution G A downstream_gene_variant SKCA-BR 15 51744528 51744528 single base substitution G A intron_variant SKCA-BR 15 51744528 51744528 single base substitution G A upstream_gene_variant SKCA-BR 15 51745399 51745399 single base substitution C A downstream_gene_variant SKCA-BR 15 51745399 51745399 single base substitution C A intron_variant SKCA-BR 15 51745399 51745399 single base substitution C A upstream_gene_variant SKCA-BR 15 51746591 51746591 single base substitution A G downstream_gene_variant SKCA-BR 15 51746591 51746591 single base substitution A G intron_variant SKCA-BR 15 51746591 51746591 single base substitution A G upstream_gene_variant SKCA-BR 15 51750350 51750350 single base substitution G A downstream_gene_variant SKCA-BR 15 51750350 51750350 single base substitution G A intron_variant SKCA-BR 15 51750350 51750350 single base substitution G A upstream_gene_variant SKCA-BR 15 51750609 51750609 single base substitution C T downstream_gene_variant SKCA-BR 15 51750609 51750609 single base substitution C T intron_variant SKCA-BR 15 51750609 51750609 single base substitution C T upstream_gene_variant SKCA-BR 15 51753939 51753939 single base substitution G A downstream_gene_variant SKCA-BR 15 51753939 51753939 single base substitution G A intron_variant SKCA-BR 15 51753939 51753939 single base substitution G A upstream_gene_variant SKCA-BR 15 51755033 51755033 single base substitution C A downstream_gene_variant SKCA-BR 15 51755033 51755033 single base substitution C A intron_variant SKCA-BR 15 51755033 51755033 single base substitution C A upstream_gene_variant SKCA-BR 15 51757911 51757911 single base substitution G C intron_variant SKCA-BR 15 51758432 51758432 single base substitution G A exon_variant SKCA-BR 15 51758432 51758432 single base substitution G A missense_variant A1853V 5558C>T SKCA-BR 15 51758432 51758432 single base substitution G A missense_variant A2489V 7466C>T SKCA-BR 15 51758432 51758432 single base substitution G A missense_variant A2490V 7469C>T SKCA-BR 15 51758432 51758432 single base substitution G A missense_variant A614V 1841C>T SKCA-BR 15 51759074 51759074 single base substitution G A intron_variant SKCA-BR 15 51759473 51759473 single base substitution G A intron_variant SKCA-BR 15 51759627 51759627 single base substitution G A intron_variant SKCA-BR 15 51759926 51759926 insertion of <=200bp - CT intron_variant SKCA-BR 15 51760425 51760425 single base substitution T C intron_variant SKCA-BR 15 51765191 51765191 insertion of <=200bp - ACT intron_variant SKCA-BR 15 51765191 51765191 insertion of <=200bp - ACT upstream_gene_variant SKCA-BR 15 51765947 51765947 single base substitution G A intron_variant SKCA-BR 15 51765947 51765947 single base substitution G A upstream_gene_variant SKCA-BR 15 51769046 51769046 single base substitution A C intron_variant SKCA-BR 15 51770295 51770295 single base substitution G A intron_variant SKCA-BR 15 51782978 51782978 single base substitution C A intron_variant SKCA-BR 15 51788874 51788874 single base substitution G A intron_variant SKCA-BR 15 51788991 51788991 single base substitution G C intron_variant SKCA-BR 15 51791397 51791397 single base substitution G A intron_variant SKCA-BR 15 51791397 51791397 single base substitution G A missense_variant P1342S 4024C>T SKCA-BR 15 51791559 51791559 single base substitution A G intron_variant SKCA-BR 15 51791559 51791559 single base substitution A G missense_variant S1288P 3862T>C SKCA-BR 15 51793754 51793754 single base substitution A G intron_variant SKCA-BR 15 51794237 51794237 single base substitution C G intron_variant SKCA-BR 15 51794428 51794428 insertion of <=200bp - TA intron_variant SKCA-BR 15 51794503 51794503 insertion of <=200bp - TTGTGTGTG intron_variant SKCA-BR 15 51794598 51794598 single base substitution C T intron_variant SKCA-BR 15 51798132 51798132 single base substitution G A intron_variant SKCA-BR 15 51798608 51798608 single base substitution C T intron_variant SKCA-BR 15 51800059 51800059 single base substitution G A intron_variant SKCA-BR 15 51802797 51802797 single base substitution G A intron_variant SKCA-BR 15 51804119 51804119 single base substitution C T intron_variant SKCA-BR 15 51804315 51804315 single base substitution C T intron_variant SKCA-BR 15 51806872 51806872 single base substitution C A intron_variant SKCA-BR 15 51807021 51807022 deletion of <=200bp GA - intron_variant SKCA-BR 15 51807039 51807039 single base substitution G A intron_variant SKCA-BR 15 51807406 51807406 single base substitution C G intron_variant SKCA-BR 15 51808339 51808339 single base substitution C T intron_variant SKCA-BR 15 51811261 51811261 single base substitution G A intron_variant SKCA-BR 15 51813611 51813623 deletion of <=200bp CTAGTAGTAGTAG - intron_variant SKCA-BR 15 51813649 51813649 single base substitution A G intron_variant SKCA-BR 15 51814061 51814061 single base substitution G A intron_variant SKCA-BR 15 51815414 51815414 single base substitution G A intron_variant SKCA-BR 15 51815860 51815860 insertion of <=200bp - ACAGAGGCAGACTG intron_variant SKCA-BR 15 51818622 51818622 single base substitution G A intron_variant SKCA-BR 15 51819068 51819068 single base substitution G A intron_variant SKCA-BR 15 51819500 51819500 single base substitution C T intron_variant SKCA-BR 15 51819507 51819507 single base substitution G A intron_variant SKCA-BR 15 51822192 51822192 single base substitution G A intron_variant SKCA-BR 15 51824957 51824957 single base substitution G A intron_variant SKCA-BR 15 51825659 51825659 single base substitution A T intron_variant SKCA-BR 15 51830233 51830233 single base substitution G A intron_variant SKCA-BR 15 51831171 51831171 single base substitution G A intron_variant SKCA-BR 15 51832345 51832345 single base substitution G T intron_variant SKCA-BR 15 51832374 51832374 single base substitution C T intron_variant SKCA-BR 15 51832465 51832465 single base substitution G A intron_variant SKCA-BR 15 51836686 51836686 single base substitution C T downstream_gene_variant SKCA-BR 15 51836686 51836686 single base substitution C T intron_variant SKCA-BR 15 51838190 51838190 single base substitution G A downstream_gene_variant SKCA-BR 15 51838190 51838190 single base substitution G A intron_variant SKCA-BR 15 51840413 51840413 single base substitution G A intron_variant SKCA-BR 15 51842110 51842110 single base substitution C T intron_variant SKCA-BR 15 51842344 51842344 single base substitution A G intron_variant SKCA-BR 15 51842688 51842688 single base substitution T A intron_variant SKCA-BR 15 51846451 51846451 single base substitution G A intron_variant SKCA-BR 15 51847593 51847593 single base substitution G C intron_variant SKCA-BR 15 51848196 51848196 single base substitution G A intron_variant SKCA-BR 15 51848685 51848685 single base substitution G C intron_variant SKCA-BR 15 51849686 51849686 single base substitution C T intron_variant SKCA-BR 15 51851605 51851605 single base substitution G A intron_variant SKCA-BR 15 51852647 51852647 single base substitution T A intron_variant SKCA-BR 15 51852651 51852651 single base substitution T A intron_variant SKCA-BR 15 51852681 51852681 single base substitution T A intron_variant SKCA-BR 15 51852885 51852885 single base substitution G A intron_variant SKCA-BR 15 51856066 51856066 single base substitution T A downstream_gene_variant SKCA-BR 15 51856066 51856066 single base substitution T A intron_variant SKCA-BR 15 51856929 51856929 single base substitution G A downstream_gene_variant SKCA-BR 15 51856929 51856929 single base substitution G A intron_variant SKCA-BR 15 51859462 51859462 single base substitution A C exon_variant SKCA-BR 15 51859462 51859462 single base substitution A C intron_variant SKCA-BR 15 51862552 51862552 single base substitution T C intron_variant SKCA-BR 15 51864463 51864463 single base substitution G C intron_variant SKCA-BR 15 51864465 51864465 single base substitution G A intron_variant SKCA-BR 15 51865483 51865483 single base substitution G A intron_variant SKCA-BR 15 51867191 51867191 single base substitution C G intron_variant SKCA-BR 15 51868373 51868373 single base substitution A G exon_variant SKCA-BR 15 51868373 51868373 single base substitution A G synonymous_variant Y31Y 93T>C SKCA-BR 15 51873582 51873582 single base substitution C T intron_variant SKCA-BR 15 51873583 51873583 single base substitution C T intron_variant SKCA-BR 15 51875014 51875014 single base substitution G A intron_variant SKCA-BR 15 51875318 51875318 single base substitution C T intron_variant SKCA-BR 15 51875646 51875646 single base substitution T C intron_variant SKCA-BR 15 51877397 51877397 single base substitution A T intron_variant SKCA-BR 15 51880012 51880012 single base substitution T A intron_variant SKCA-BR 15 51882080 51882080 single base substitution C T intron_variant SKCA-BR 15 51882303 51882303 single base substitution G A intron_variant SKCA-BR 15 51884583 51884583 single base substitution G A intron_variant SKCA-BR 15 51885891 51885891 single base substitution A C intron_variant SKCA-BR 15 51886651 51886651 single base substitution G A intron_variant SKCA-BR 15 51893104 51893104 single base substitution T C intron_variant SKCA-BR 15 51893174 51893174 single base substitution G A intron_variant SKCA-BR 15 51896513 51896513 single base substitution G A intron_variant SKCA-BR 15 51896513 51896513 single base substitution G A upstream_gene_variant SKCA-BR 15 51896909 51896909 single base substitution G A intron_variant SKCA-BR 15 51896909 51896909 single base substitution G A upstream_gene_variant SKCA-BR 15 51897238 51897238 insertion of <=200bp - CA intron_variant SKCA-BR 15 51897238 51897238 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 15 51900649 51900649 single base substitution T C intron_variant SKCA-BR 15 51900649 51900649 single base substitution T C upstream_gene_variant SKCA-BR 15 51900959 51900960 deletion of <=200bp GA - intron_variant SKCA-BR 15 51902127 51902128 deletion of <=200bp TA - intron_variant SKCA-BR 15 51907536 51907536 single base substitution G A intron_variant SKCA-BR 15 51907567 51907567 single base substitution G A intron_variant SKCA-BR 15 51908481 51908481 single base substitution G A intron_variant SKCA-BR 15 51908498 51908498 single base substitution C T intron_variant SKCA-BR 15 51909776 51909776 single base substitution G C intron_variant SKCA-BR 15 51912971 51912971 single base substitution A G intron_variant SKCA-BR 15 51913085 51913085 single base substitution A C intron_variant SKCA-BR 15 51913098 51913098 single base substitution G T intron_variant SKCA-BR 15 51914807 51914807 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 15 51914807 51914807 single base substitution G A exon_variant SKCA-BR 15 51914980 51914980 single base substitution C G 5_prime_UTR_variant SKCA-BR 15 51914980 51914980 single base substitution C G upstream_gene_variant SKCM-US 15 51741329 51741329 single base substitution G A downstream_gene_variant SKCM-US 15 51741329 51741329 single base substitution G A exon_variant SKCM-US 15 51741329 51741329 single base substitution G A missense_variant S1134F 3401C>T SKCM-US 15 51741329 51741329 single base substitution G A missense_variant S2352F 7055C>T SKCM-US 15 51741329 51741329 single base substitution G A missense_variant S2988F 8963C>T SKCM-US 15 51741329 51741329 single base substitution G A missense_variant S2989F 8966C>T SKCM-US 15 51741366 51741366 single base substitution G A downstream_gene_variant SKCM-US 15 51741366 51741366 single base substitution G A exon_variant SKCM-US 15 51741366 51741366 single base substitution G A synonymous_variant L1122L 3364C>T SKCM-US 15 51741366 51741366 single base substitution G A synonymous_variant L2340L 7018C>T SKCM-US 15 51741366 51741366 single base substitution G A synonymous_variant L2976L 8926C>T SKCM-US 15 51741366 51741366 single base substitution G A synonymous_variant L2977L 8929C>T SKCM-US 15 51742477 51742477 single base substitution G A downstream_gene_variant SKCM-US 15 51742477 51742477 single base substitution G A exon_variant SKCM-US 15 51742477 51742477 single base substitution G A missense_variant S1063L 3188C>T SKCM-US 15 51742477 51742477 single base substitution G A missense_variant S2281L 6842C>T SKCM-US 15 51742477 51742477 single base substitution G A missense_variant S2917L 8750C>T SKCM-US 15 51742477 51742477 single base substitution G A missense_variant S2918L 8753C>T SKCM-US 15 51742477 51742477 single base substitution G A synonymous_variant L74L 222C>T SKCM-US 15 51742485 51742485 single base substitution G A downstream_gene_variant SKCM-US 15 51742485 51742485 single base substitution G A exon_variant SKCM-US 15 51742485 51742485 single base substitution G A missense_variant P72S 214C>T SKCM-US 15 51742485 51742485 single base substitution G A synonymous_variant L1060L 3180C>T SKCM-US 15 51742485 51742485 single base substitution G A synonymous_variant L2278L 6834C>T SKCM-US 15 51742485 51742485 single base substitution G A synonymous_variant L2914L 8742C>T SKCM-US 15 51742485 51742485 single base substitution G A synonymous_variant L2915L 8745C>T SKCM-US 15 51749620 51749620 single base substitution G A downstream_gene_variant SKCM-US 15 51749620 51749620 single base substitution G A exon_variant SKCM-US 15 51749620 51749620 single base substitution G A stop_gained Q2090* 6268C>T SKCM-US 15 51749620 51749620 single base substitution G A stop_gained Q2726* 8176C>T SKCM-US 15 51749620 51749620 single base substitution G A stop_gained Q2727* 8179C>T SKCM-US 15 51749620 51749620 single base substitution G A stop_gained Q872* 2614C>T SKCM-US 15 51749620 51749620 single base substitution G A upstream_gene_variant SKCM-US 15 51755594 51755594 single base substitution C T exon_variant SKCM-US 15 51755594 51755594 single base substitution C T intron_variant SKCM-US 15 51755594 51755594 single base substitution C T synonymous_variant K1999K 5997G>A SKCM-US 15 51755594 51755594 single base substitution C T synonymous_variant K2635K 7905G>A SKCM-US 15 51755594 51755594 single base substitution C T synonymous_variant K2636K 7908G>A SKCM-US 15 51755594 51755594 single base substitution C T synonymous_variant K760K 2280G>A SKCM-US 15 51755594 51755594 single base substitution C T upstream_gene_variant SKCM-US 15 51757773 51757773 single base substitution C T exon_variant SKCM-US 15 51757773 51757773 single base substitution C T synonymous_variant L1895L 5685G>A SKCM-US 15 51757773 51757773 single base substitution C T synonymous_variant L2531L 7593G>A SKCM-US 15 51757773 51757773 single base substitution C T synonymous_variant L2532L 7596G>A SKCM-US 15 51757773 51757773 single base substitution C T synonymous_variant L656L 1968G>A SKCM-US 15 51757791 51757791 single base substitution G A exon_variant SKCM-US 15 51757791 51757791 single base substitution G A synonymous_variant F1889F 5667C>T SKCM-US 15 51757791 51757791 single base substitution G A synonymous_variant F2525F 7575C>T SKCM-US 15 51757791 51757791 single base substitution G A synonymous_variant F2526F 7578C>T SKCM-US 15 51757791 51757791 single base substitution G A synonymous_variant F650F 1950C>T SKCM-US 15 51758421 51758421 single base substitution C T exon_variant SKCM-US 15 51758421 51758421 single base substitution C T missense_variant D1857N 5569G>A SKCM-US 15 51758421 51758421 single base substitution C T missense_variant D2493N 7477G>A SKCM-US 15 51758421 51758421 single base substitution C T missense_variant D2494N 7480G>A SKCM-US 15 51758421 51758421 single base substitution C T missense_variant D618N 1852G>A SKCM-US 15 51763533 51763533 single base substitution G A exon_variant SKCM-US 15 51763533 51763533 single base substitution G A missense_variant P1790S 5368C>T SKCM-US 15 51763533 51763533 single base substitution G A missense_variant P2426S 7276C>T SKCM-US 15 51763533 51763533 single base substitution G A missense_variant P2427S 7279C>T SKCM-US 15 51763533 51763533 single base substitution G A missense_variant P551S 1651C>T SKCM-US 15 51763533 51763533 single base substitution G A upstream_gene_variant SKCM-US 15 51763564 51763564 single base substitution G A synonymous_variant H1779H 5337C>T SKCM-US 15 51763564 51763564 single base substitution G A synonymous_variant H2415H 7245C>T SKCM-US 15 51763564 51763564 single base substitution G A synonymous_variant H2416H 7248C>T SKCM-US 15 51763564 51763564 single base substitution G A synonymous_variant H540H 1620C>T SKCM-US 15 51763564 51763564 single base substitution G A upstream_gene_variant SKCM-US 15 51766543 51766543 single base substitution G A missense_variant S1767L 5300C>T SKCM-US 15 51766543 51766543 single base substitution G A missense_variant S2403L 7208C>T SKCM-US 15 51766543 51766543 single base substitution G A missense_variant S2404L 7211C>T SKCM-US 15 51766543 51766543 single base substitution G A missense_variant S528L 1583C>T SKCM-US 15 51766543 51766543 single base substitution G A upstream_gene_variant SKCM-US 15 51766660 51766660 single base substitution G A missense_variant S1728F 5183C>T SKCM-US 15 51766660 51766660 single base substitution G A missense_variant S2364F 7091C>T SKCM-US 15 51766660 51766660 single base substitution G A missense_variant S2365F 7094C>T SKCM-US 15 51766660 51766660 single base substitution G A missense_variant S489F 1466C>T SKCM-US 15 51766660 51766660 single base substitution G A upstream_gene_variant SKCM-US 15 51772772 51772772 single base substitution C T missense_variant M1541I 4623G>A SKCM-US 15 51772772 51772772 single base substitution C T missense_variant M2177I 6531G>A SKCM-US 15 51772772 51772772 single base substitution C T missense_variant M301I 903G>A SKCM-US 15 51772866 51772866 single base substitution G A missense_variant S1510L 4529C>T SKCM-US 15 51772866 51772866 single base substitution G A missense_variant S2146L 6437C>T SKCM-US 15 51772866 51772866 single base substitution G A missense_variant S270L 809C>T SKCM-US 15 51772994 51772994 single base substitution G A synonymous_variant S1467S 4401C>T SKCM-US 15 51772994 51772994 single base substitution G A synonymous_variant S2103S 6309C>T SKCM-US 15 51772994 51772994 single base substitution G A synonymous_variant S227S 681C>T SKCM-US 15 51773152 51773152 single base substitution G A missense_variant L1415F 4243C>T SKCM-US 15 51773152 51773152 single base substitution G A missense_variant L175F 523C>T SKCM-US 15 51773152 51773152 single base substitution G A missense_variant L2051F 6151C>T SKCM-US 15 51773239 51773239 deletion of <=200bp T - frameshift_variant T1386 SKCM-US 15 51773239 51773239 deletion of <=200bp T - frameshift_variant T146 SKCM-US 15 51773239 51773239 deletion of <=200bp T - frameshift_variant T2022 SKCM-US 15 51773525 51773525 single base substitution G A synonymous_variant F1290F 3870C>T SKCM-US 15 51773525 51773525 single base substitution G A synonymous_variant F1926F 5778C>T SKCM-US 15 51773525 51773525 single base substitution G A synonymous_variant F50F 150C>T SKCM-US 15 51773612 51773612 single base substitution G A synonymous_variant C1261C 3783C>T SKCM-US 15 51773612 51773612 single base substitution G A synonymous_variant C1897C 5691C>T SKCM-US 15 51773612 51773612 single base substitution G A synonymous_variant C21C 63C>T SKCM-US 15 51778369 51778369 single base substitution G A missense_variant P1159S 3475C>T SKCM-US 15 51778369 51778369 single base substitution G A missense_variant P1795S 5383C>T SKCM-US 15 51778369 51778369 single base substitution G A upstream_gene_variant SKCM-US 15 51780227 51780227 single base substitution G A missense_variant S1078F 3233C>T SKCM-US 15 51780227 51780227 single base substitution G A missense_variant S1714F 5141C>T SKCM-US 15 51783792 51783792 single base substitution G T synonymous_variant R1010R 3028C>A SKCM-US 15 51783792 51783792 single base substitution G T synonymous_variant R1646R 4936C>A SKCM-US 15 51790919 51790919 single base substitution T C intron_variant SKCM-US 15 51790919 51790919 single base substitution T C missense_variant Y1501C 4502A>G SKCM-US 15 51791010 51791010 single base substitution G A intron_variant SKCM-US 15 51791010 51791010 single base substitution G A synonymous_variant L1471L 4411C>T SKCM-US 15 51791142 51791142 single base substitution G A intron_variant SKCM-US 15 51791142 51791142 single base substitution G A missense_variant P1427S 4279C>T SKCM-US 15 51791231 51791231 single base substitution C T intron_variant SKCM-US 15 51791231 51791231 single base substitution C T missense_variant R1397Q 4190G>A SKCM-US 15 51791364 51791364 single base substitution A G intron_variant SKCM-US 15 51791364 51791364 single base substitution A G synonymous_variant L1353L 4057T>C SKCM-US 15 51791468 51791468 single base substitution G A intron_variant SKCM-US 15 51791468 51791468 single base substitution G A missense_variant S1318F 3953C>T SKCM-US 15 51791510 51791510 single base substitution T G intron_variant SKCM-US 15 51791510 51791510 single base substitution T G missense_variant N1304T 3911A>C SKCM-US 15 51792133 51792133 single base substitution A T intron_variant SKCM-US 15 51792133 51792133 single base substitution A T synonymous_variant V1096V 3288T>A SKCM-US 15 51792261 51792261 single base substitution T G intron_variant SKCM-US 15 51792261 51792261 single base substitution T G missense_variant M1054L 3160A>C SKCM-US 15 51792266 51792266 single base substitution G A intron_variant SKCM-US 15 51792266 51792266 single base substitution G A missense_variant P1052L 3155C>T SKCM-US 15 51795147 51795147 single base substitution G A intron_variant SKCM-US 15 51795147 51795147 single base substitution G A missense_variant P950S 2848C>T SKCM-US 15 51795149 51795149 single base substitution G A intron_variant SKCM-US 15 51795149 51795149 single base substitution G A missense_variant S949F 2846C>T SKCM-US 15 51795182 51795182 single base substitution C A intron_variant SKCM-US 15 51795182 51795182 single base substitution C A missense_variant G938V 2813G>T SKCM-US 15 51795209 51795209 single base substitution G A intron_variant SKCM-US 15 51795209 51795209 single base substitution G A missense_variant S929F 2786C>T SKCM-US 15 51828531 51828531 single base substitution G A missense_variant H716Y 2146C>T SKCM-US 15 51828912 51828912 single base substitution G A missense_variant P589S 1765C>T SKCM-US 15 51829948 51829948 single base substitution G A synonymous_variant L452L 1354C>T SKCM-US 15 51829950 51829950 single base substitution G A missense_variant S451F 1352C>T SKCM-US 15 51830432 51830432 single base substitution A G synonymous_variant G441G 1323T>C SKCM-US 15 51830440 51830440 single base substitution C A stop_gained E439* 1315G>T SKCM-US 15 51830595 51830595 single base substitution C T missense_variant G387D 1160G>A SKCM-US 15 51834628 51834628 single base substitution G A downstream_gene_variant SKCM-US 15 51834628 51834628 single base substitution G A missense_variant P336L 1007C>T SKCM-US 15 51837933 51837933 single base substitution T A downstream_gene_variant SKCM-US 15 51837933 51837933 single base substitution T A synonymous_variant S259S 777A>T SKCM-US 15 51839457 51839457 single base substitution G A downstream_gene_variant SKCM-US 15 51839457 51839457 single base substitution G A missense_variant S239L 716C>T SKCM-US 15 51839476 51839476 single base substitution G A downstream_gene_variant SKCM-US 15 51839476 51839476 single base substitution G A stop_gained R233* 697C>T SKCM-US 15 51839578 51839578 single base substitution G A exon_variant SKCM-US 15 51839578 51839578 single base substitution G A missense_variant P199S 595C>T SKCM-US 15 51857296 51857296 single base substitution C T downstream_gene_variant SKCM-US 15 51857296 51857296 single base substitution C T exon_variant SKCM-US 15 51857296 51857296 single base substitution C T stop_gained W118* 353G>A STAD-US 15 51742428 51742428 single base substitution C T 3_prime_UTR_variant STAD-US 15 51742428 51742428 single base substitution C T downstream_gene_variant STAD-US 15 51742428 51742428 single base substitution C T exon_variant STAD-US 15 51742428 51742428 single base substitution C T synonymous_variant Q1079Q 3237G>A STAD-US 15 51742428 51742428 single base substitution C T synonymous_variant Q2297Q 6891G>A STAD-US 15 51742428 51742428 single base substitution C T synonymous_variant Q2933Q 8799G>A STAD-US 15 51742428 51742428 single base substitution C T synonymous_variant Q2934Q 8802G>A STAD-US 15 51749571 51749571 single base substitution G C downstream_gene_variant STAD-US 15 51749571 51749571 single base substitution G C exon_variant STAD-US 15 51749571 51749571 single base substitution G C missense_variant S2106C 6317C>G STAD-US 15 51749571 51749571 single base substitution G C missense_variant S2742C 8225C>G STAD-US 15 51749571 51749571 single base substitution G C missense_variant S2743C 8228C>G STAD-US 15 51749571 51749571 single base substitution G C missense_variant S888C 2663C>G STAD-US 15 51749571 51749571 single base substitution G C upstream_gene_variant STAD-US 15 51750813 51750813 single base substitution A G 3_prime_UTR_variant STAD-US 15 51750813 51750813 single base substitution A G downstream_gene_variant STAD-US 15 51750813 51750813 single base substitution A G exon_variant STAD-US 15 51750813 51750813 single base substitution A G synonymous_variant N2038N 6114T>C STAD-US 15 51750813 51750813 single base substitution A G synonymous_variant N2674N 8022T>C STAD-US 15 51750813 51750813 single base substitution A G synonymous_variant N2675N 8025T>C STAD-US 15 51750813 51750813 single base substitution A G synonymous_variant N820N 2460T>C STAD-US 15 51750813 51750813 single base substitution A G upstream_gene_variant STAD-US 15 51755589 51755589 single base substitution C A exon_variant STAD-US 15 51755589 51755589 single base substitution C A intron_variant STAD-US 15 51755589 51755589 single base substitution C A missense_variant R2001I 6002G>T STAD-US 15 51755589 51755589 single base substitution C A missense_variant R2637I 7910G>T STAD-US 15 51755589 51755589 single base substitution C A missense_variant R2638I 7913G>T STAD-US 15 51755589 51755589 single base substitution C A missense_variant R762I 2285G>T STAD-US 15 51755589 51755589 single base substitution C A upstream_gene_variant STAD-US 15 51763435 51763435 single base substitution A C exon_variant STAD-US 15 51763435 51763435 single base substitution A C missense_variant D1822E 5466T>G STAD-US 15 51763435 51763435 single base substitution A C missense_variant D2458E 7374T>G STAD-US 15 51763435 51763435 single base substitution A C missense_variant D2459E 7377T>G STAD-US 15 51763435 51763435 single base substitution A C missense_variant D583E 1749T>G STAD-US 15 51763435 51763435 single base substitution A C upstream_gene_variant STAD-US 15 51763453 51763453 single base substitution G A exon_variant STAD-US 15 51763453 51763453 single base substitution G A synonymous_variant P1816P 5448C>T STAD-US 15 51763453 51763453 single base substitution G A synonymous_variant P2452P 7356C>T STAD-US 15 51763453 51763453 single base substitution G A synonymous_variant P2453P 7359C>T STAD-US 15 51763453 51763453 single base substitution G A synonymous_variant P577P 1731C>T STAD-US 15 51763453 51763453 single base substitution G A upstream_gene_variant STAD-US 15 51772201 51772201 single base substitution G C missense_variant L1598V 4792C>G STAD-US 15 51772201 51772201 single base substitution G C missense_variant L2234V 6700C>G STAD-US 15 51772201 51772201 single base substitution G C missense_variant L358V 1072C>G STAD-US 15 51772992 51772992 single base substitution T C missense_variant K1468R 4403A>G STAD-US 15 51772992 51772992 single base substitution T C missense_variant K2104R 6311A>G STAD-US 15 51772992 51772992 single base substitution T C missense_variant K228R 683A>G STAD-US 15 51773499 51773499 single base substitution G T missense_variant P1299H 3896C>A STAD-US 15 51773499 51773499 single base substitution G T missense_variant P1935H 5804C>A STAD-US 15 51773499 51773499 single base substitution G T missense_variant P59H 176C>A STAD-US 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K1285K? STAD-US 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K1921K? STAD-US 15 51773540 51773540 insertion of <=200bp - T frameshift_variant K45K? STAD-US 15 51773769 51773769 single base substitution C T missense_variant R1209Q 3626G>A STAD-US 15 51773769 51773769 single base substitution C T missense_variant R1845Q 5534G>A STAD-US 15 51773769 51773769 single base substitution C T upstream_gene_variant STAD-US 15 51773773 51773773 single base substitution G T missense_variant L1208I 3622C>A STAD-US 15 51773773 51773773 single base substitution G T missense_variant L1844I 5530C>A STAD-US 15 51773773 51773773 single base substitution G T upstream_gene_variant STAD-US 15 51778519 51778519 deletion of <=200bp T - frameshift_variant M1109 STAD-US 15 51778519 51778519 deletion of <=200bp T - frameshift_variant M1745 STAD-US 15 51778519 51778519 deletion of <=200bp T - upstream_gene_variant STAD-US 15 51780825 51780825 insertion of <=200bp - A frameshift_variant F1021F? STAD-US 15 51780825 51780825 insertion of <=200bp - A frameshift_variant F1657F? STAD-US 15 51783905 51783905 single base substitution T G missense_variant E1608A 4823A>C STAD-US 15 51783905 51783905 single base substitution T G missense_variant E972A 2915A>C STAD-US 15 51790812 51790812 single base substitution A T intron_variant STAD-US 15 51790812 51790812 single base substitution A T missense_variant L1537M 4609T>A STAD-US 15 51791197 51791197 single base substitution T G intron_variant STAD-US 15 51791197 51791197 single base substitution T G missense_variant E1408D 4224A>C STAD-US 15 51792058 51792058 single base substitution T C intron_variant STAD-US 15 51792058 51792058 single base substitution T C synonymous_variant Q1121Q 3363A>G STAD-US 15 51799444 51799444 single base substitution C T missense_variant R884H 2651G>A STAD-US 15 51827880 51827880 single base substitution A G synonymous_variant L806L 2416T>C STAD-US 15 51828437 51828437 single base substitution C T missense_variant R747Q 2240G>A STAD-US 15 51828742 51828742 single base substitution T A missense_variant R645S 1935A>T STAD-US 15 51828804 51828804 single base substitution C T missense_variant A625T 1873G>A STAD-US 15 51829690 51829690 single base substitution C G missense_variant V538L 1612G>C STAD-US 15 51830437 51830437 single base substitution G A missense_variant R440W 1318C>T STAD-US 15 51837811 51837811 single base substitution C T downstream_gene_variant STAD-US 15 51837811 51837811 single base substitution C T missense_variant R300K 899G>A STAD-US 15 51856325 51856325 single base substitution C T downstream_gene_variant STAD-US 15 51856325 51856325 single base substitution C T exon_variant STAD-US 15 51856325 51856325 single base substitution C T missense_variant C166Y 497G>A STAD-US 15 51857323 51857323 insertion of <=200bp - A downstream_gene_variant STAD-US 15 51857323 51857323 insertion of <=200bp - A exon_variant STAD-US 15 51857323 51857323 insertion of <=200bp - A frameshift_variant L109F? STAD-US 15 51857327 51857327 single base substitution A C downstream_gene_variant STAD-US 15 51857327 51857327 single base substitution A C exon_variant STAD-US 15 51857327 51857327 single base substitution A C missense_variant F108V 322T>G STAD-US 15 51860757 51860757 single base substitution T A splice_acceptor_variant STAD-US 15 51868358 51868358 single base substitution A G exon_variant STAD-US 15 51868358 51868358 single base substitution A G synonymous_variant D36D 108T>C THCA-US 15 51791873 51791873 single base substitution A G intron_variant THCA-US 15 51791873 51791873 single base substitution A G missense_variant L1183P 3548T>C THCA-US 15 51837864 51837864 single base substitution C A downstream_gene_variant THCA-US 15 51837864 51837864 single base substitution C A missense_variant Q282H 846G>T UCEC-US 15 51741195 51741195 single base substitution G T downstream_gene_variant UCEC-US 15 51741195 51741195 single base substitution G T exon_variant UCEC-US 15 51741195 51741195 single base substitution G T missense_variant L1179I 3535C>A UCEC-US 15 51741195 51741195 single base substitution G T missense_variant L2397I 7189C>A UCEC-US 15 51741195 51741195 single base substitution G T missense_variant L3033I 9097C>A UCEC-US 15 51741195 51741195 single base substitution G T missense_variant L3034I 9100C>A UCEC-US 15 51742382 51742382 single base substitution C T downstream_gene_variant UCEC-US 15 51742382 51742382 single base substitution C T exon_variant UCEC-US 15 51742382 51742382 single base substitution C T missense_variant A1095T 3283G>A UCEC-US 15 51742382 51742382 single base substitution C T missense_variant A2313T 6937G>A UCEC-US 15 51742382 51742382 single base substitution C T missense_variant A2949T 8845G>A UCEC-US 15 51742382 51742382 single base substitution C T missense_variant A2950T 8848G>A UCEC-US 15 51742425 51742425 single base substitution G T 3_prime_UTR_variant UCEC-US 15 51742425 51742425 single base substitution G T downstream_gene_variant UCEC-US 15 51742425 51742425 single base substitution G T exon_variant UCEC-US 15 51742425 51742425 single base substitution G T synonymous_variant L1080L 3240C>A UCEC-US 15 51742425 51742425 single base substitution G T synonymous_variant L2298L 6894C>A UCEC-US 15 51742425 51742425 single base substitution G T synonymous_variant L2934L 8802C>A UCEC-US 15 51742425 51742425 single base substitution G T synonymous_variant L2935L 8805C>A UCEC-US 15 51743895 51743895 single base substitution C A downstream_gene_variant UCEC-US 15 51743895 51743895 single base substitution C A intron_variant UCEC-US 15 51743895 51743895 single base substitution C A splice_acceptor_variant UCEC-US 15 51743895 51743895 single base substitution C A upstream_gene_variant UCEC-US 15 51747401 51747401 single base substitution A C downstream_gene_variant UCEC-US 15 51747401 51747401 single base substitution A C exon_variant UCEC-US 15 51747401 51747401 single base substitution A C missense_variant F2193V 6577T>G UCEC-US 15 51747401 51747401 single base substitution A C missense_variant F2829V 8485T>G UCEC-US 15 51747401 51747401 single base substitution A C missense_variant F2830V 8488T>G UCEC-US 15 51747401 51747401 single base substitution A C missense_variant F4V 10T>G UCEC-US 15 51747401 51747401 single base substitution A C missense_variant F975V 2923T>G UCEC-US 15 51747401 51747401 single base substitution A C upstream_gene_variant UCEC-US 15 51748267 51748267 single base substitution T C downstream_gene_variant UCEC-US 15 51748267 51748267 single base substitution T C exon_variant UCEC-US 15 51748267 51748267 single base substitution T C missense_variant N2183S 6548A>G UCEC-US 15 51748267 51748267 single base substitution T C missense_variant N2819S 8456A>G UCEC-US 15 51748267 51748267 single base substitution T C missense_variant N2820S 8459A>G UCEC-US 15 51748267 51748267 single base substitution T C missense_variant N965S 2894A>G UCEC-US 15 51748267 51748267 single base substitution T C upstream_gene_variant UCEC-US 15 51757797 51757797 single base substitution C A exon_variant UCEC-US 15 51757797 51757797 single base substitution C A missense_variant K1887N 5661G>T UCEC-US 15 51757797 51757797 single base substitution C A missense_variant K2523N 7569G>T UCEC-US 15 51757797 51757797 single base substitution C A missense_variant K2524N 7572G>T UCEC-US 15 51757797 51757797 single base substitution C A missense_variant K648N 1944G>T UCEC-US 15 51763591 51763591 single base substitution A G synonymous_variant P1770P 5310T>C UCEC-US 15 51763591 51763591 single base substitution A G synonymous_variant P2406P 7218T>C UCEC-US 15 51763591 51763591 single base substitution A G synonymous_variant P2407P 7221T>C UCEC-US 15 51763591 51763591 single base substitution A G synonymous_variant P531P 1593T>C UCEC-US 15 51763591 51763591 single base substitution A G upstream_gene_variant UCEC-US 15 51766565 51766565 single base substitution G A stop_gained R1760* 5278C>T UCEC-US 15 51766565 51766565 single base substitution G A stop_gained R2396* 7186C>T UCEC-US 15 51766565 51766565 single base substitution G A stop_gained R2397* 7189C>T UCEC-US 15 51766565 51766565 single base substitution G A stop_gained R521* 1561C>T UCEC-US 15 51766565 51766565 single base substitution G A upstream_gene_variant UCEC-US 15 51766643 51766643 single base substitution G A missense_variant R1734W 5200C>T UCEC-US 15 51766643 51766643 single base substitution G A missense_variant R2370W 7108C>T UCEC-US 15 51766643 51766643 single base substitution G A missense_variant R2371W 7111C>T UCEC-US 15 51766643 51766643 single base substitution G A missense_variant R495W 1483C>T UCEC-US 15 51766643 51766643 single base substitution G A upstream_gene_variant UCEC-US 15 51766690 51766690 single base substitution C T missense_variant S1718N 5153G>A UCEC-US 15 51766690 51766690 single base substitution C T missense_variant S2354N 7061G>A UCEC-US 15 51766690 51766690 single base substitution C T missense_variant S2355N 7064G>A UCEC-US 15 51766690 51766690 single base substitution C T missense_variant S479N 1436G>A UCEC-US 15 51766690 51766690 single base substitution C T upstream_gene_variant UCEC-US 15 51772191 51772191 single base substitution A C missense_variant I1601S 4802T>G UCEC-US 15 51772191 51772191 single base substitution A C missense_variant I2237S 6710T>G UCEC-US 15 51772191 51772191 single base substitution A C missense_variant I361S 1082T>G UCEC-US 15 51772262 51772262 single base substitution C T synonymous_variant A1577A 4731G>A UCEC-US 15 51772262 51772262 single base substitution C T synonymous_variant A2213A 6639G>A UCEC-US 15 51772262 51772262 single base substitution C T synonymous_variant A337A 1011G>A UCEC-US 15 51772896 51772896 single base substitution G A missense_variant A1500V 4499C>T UCEC-US 15 51772896 51772896 single base substitution G A missense_variant A2136V 6407C>T UCEC-US 15 51772896 51772896 single base substitution G A missense_variant A260V 779C>T UCEC-US 15 51772990 51772990 single base substitution C T missense_variant V1469I 4405G>A UCEC-US 15 51772990 51772990 single base substitution C T missense_variant V2105I 6313G>A UCEC-US 15 51772990 51772990 single base substitution C T missense_variant V229I 685G>A UCEC-US 15 51773042 51773042 single base substitution T C missense_variant I1451M 4353A>G UCEC-US 15 51773042 51773042 single base substitution T C missense_variant I2087M 6261A>G UCEC-US 15 51773042 51773042 single base substitution T C missense_variant I211M 633A>G UCEC-US 15 51773810 51773810 single base substitution C T synonymous_variant K1195K 3585G>A UCEC-US 15 51773810 51773810 single base substitution C T synonymous_variant K1831K 5493G>A UCEC-US 15 51773810 51773810 single base substitution C T upstream_gene_variant UCEC-US 15 51778323 51778323 single base substitution C T missense_variant R1174Q 3521G>A UCEC-US 15 51778323 51778323 single base substitution C T missense_variant R1810Q 5429G>A UCEC-US 15 51778323 51778323 single base substitution C T upstream_gene_variant UCEC-US 15 51778324 51778324 single base substitution G A stop_gained R1174* 3520C>T UCEC-US 15 51778324 51778324 single base substitution G A stop_gained R1810* 5428C>T UCEC-US 15 51778324 51778324 single base substitution G A upstream_gene_variant UCEC-US 15 51780829 51780829 single base substitution G T missense_variant S1020Y 3059C>A UCEC-US 15 51780829 51780829 single base substitution G T missense_variant S1656Y 4967C>A UCEC-US 15 51787269 51787269 single base substitution G T missense_variant L1579I 4735C>A UCEC-US 15 51787269 51787269 single base substitution G T missense_variant L943I 2827C>A UCEC-US 15 51787283 51787283 single base substitution C T missense_variant R1574H 4721G>A UCEC-US 15 51787283 51787283 single base substitution C T missense_variant R938H 2813G>A UCEC-US 15 51787326 51787326 single base substitution C A missense_variant D1560Y 4678G>T UCEC-US 15 51787326 51787326 single base substitution C A missense_variant D924Y 2770G>T UCEC-US 15 51790759 51790759 single base substitution C A intron_variant UCEC-US 15 51790759 51790759 single base substitution C A missense_variant K1554N 4662G>T UCEC-US 15 51790926 51790926 single base substitution A C intron_variant UCEC-US 15 51790926 51790926 single base substitution A C missense_variant S1499A 4495T>G UCEC-US 15 51790985 51790985 single base substitution G A intron_variant UCEC-US 15 51790985 51790985 single base substitution G A missense_variant T1479M 4436C>T UCEC-US 15 51791178 51791178 single base substitution C A intron_variant UCEC-US 15 51791178 51791178 single base substitution C A missense_variant D1415Y 4243G>T UCEC-US 15 51791393 51791393 single base substitution G T intron_variant UCEC-US 15 51791393 51791393 single base substitution G T missense_variant T1343N 4028C>A UCEC-US 15 51791647 51791647 single base substitution C T intron_variant UCEC-US 15 51791647 51791647 single base substitution C T synonymous_variant G1258G 3774G>A UCEC-US 15 51791860 51791860 single base substitution G A intron_variant UCEC-US 15 51791860 51791860 single base substitution G A synonymous_variant V1187V 3561C>T UCEC-US 15 51791950 51791950 single base substitution C A intron_variant UCEC-US 15 51791950 51791950 single base substitution C A missense_variant K1157N 3471G>T UCEC-US 15 51792045 51792045 single base substitution C T intron_variant UCEC-US 15 51792045 51792045 single base substitution C T missense_variant D1126N 3376G>A UCEC-US 15 51792126 51792126 single base substitution C A intron_variant UCEC-US 15 51792126 51792126 single base substitution C A stop_gained E1099* 3295G>T UCEC-US 15 51792160 51792160 single base substitution C T intron_variant UCEC-US 15 51792160 51792160 single base substitution C T synonymous_variant K1087K 3261G>A UCEC-US 15 51792189 51792189 single base substitution A G intron_variant UCEC-US 15 51792189 51792189 single base substitution A G missense_variant Y1078H 3232T>C UCEC-US 15 51792233 51792233 single base substitution C G intron_variant UCEC-US 15 51792233 51792233 single base substitution C G missense_variant S1063T 3188G>C UCEC-US 15 51792406 51792406 single base substitution A C intron_variant UCEC-US 15 51792406 51792406 single base substitution A C missense_variant I1005M 3015T>G UCEC-US 15 51795105 51795105 single base substitution G T intron_variant UCEC-US 15 51795105 51795105 single base substitution G T missense_variant L964I 2890C>A UCEC-US 15 51809350 51809350 single base substitution T G missense_variant E817D 2451A>C UCEC-US 15 51828413 51828413 single base substitution G A missense_variant A755V 2264C>T UCEC-US 15 51828437 51828437 single base substitution C T missense_variant R747Q 2240G>A UCEC-US 15 51828531 51828531 single base substitution G T missense_variant H716N 2146C>A UCEC-US 15 51828614 51828614 single base substitution T G missense_variant K688T 2063A>C UCEC-US 15 51828783 51828783 single base substitution A G missense_variant S632P 1894T>C UCEC-US 15 51830521 51830521 single base substitution G A stop_gained R412* 1234C>T UCEC-US 15 51834653 51834653 single base substitution G T downstream_gene_variant UCEC-US 15 51834653 51834653 single base substitution G T missense_variant L328I 982C>A UCEC-US 15 51834686 51834686 single base substitution T A downstream_gene_variant UCEC-US 15 51834686 51834686 single base substitution T A missense_variant N317Y 949A>T UCEC-US 15 51839487 51839487 single base substitution A G downstream_gene_variant UCEC-US 15 51839487 51839487 single base substitution A G missense_variant L229S 686T>C UCEC-US 15 51856380 51856380 single base substitution C A downstream_gene_variant UCEC-US 15 51856380 51856380 single base substitution C A exon_variant UCEC-US 15 51856380 51856380 single base substitution C A stop_gained E148* 442G>T UCEC-US 15 51856382 51856382 single base substitution T G downstream_gene_variant UCEC-US 15 51856382 51856382 single base substitution T G exon_variant UCEC-US 15 51856382 51856382 single base substitution T G missense_variant E147A 440A>C UCEC-US 15 51856450 51856450 single base substitution T G downstream_gene_variant UCEC-US 15 51856450 51856450 single base substitution T G exon_variant UCEC-US 15 51856450 51856450 single base substitution T G missense_variant R124S 372A>C UCEC-US 15 51856455 51856455 single base substitution T C downstream_gene_variant UCEC-US 15 51856455 51856455 single base substitution T C missense_variant N123D 367A>G UCEC-US 15 51856455 51856455 single base substitution T C splice_region_variant UCEC-US 15 51860704 51860704 single base substitution T G exon_variant UCEC-US 15 51860704 51860704 single base substitution T G missense_variant N89H 265A>C UCEC-US 15 51868279 51868279 single base substitution C A exon_variant UCEC-US 15 51868279 51868279 single base substitution C A missense_variant V63L 187G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-D8-A27G-01 COSM3816303 c.5398C>T p.L1800F Substitution - Missense 15:51486157-51486157 - TCGA-EE-A2MJ-06 COSM3502100 c.1315G>T p.E439* Substitution - Nonsense 15:51538243-51538243 - HCC20 COSM1608471 c.4367A>G p.Y1456C Substitution - Missense 15:51498857-51498857 - TCGA-D8-A1JA-01 COSM3816310 c.1775C>G p.S592* Substitution - Nonsense 15:51536705-51536705 - TCGA-A8-A0A6-01 COSM3816312 c.862A>C p.T288P Substitution - Missense 15:51545651-51545651 - TCGA-BR-8589-01 COSM4055517 c.4823A>C p.E1608A Substitution - Missense 15:51491708-51491708 - B106-Tumor COSM1749205 c.4676G>A p.R1559K Substitution - Missense 15:51495131-51495131 - TCGA-EK-A2PM-01 COSM4831425 c.4599C>T p.F1533F Substitution - coding silent 15:51498625-51498625 - SNU-175 COSM962715 c.5428C>T p.R1810* Substitution - Nonsense 15:51486127-51486127 - TCGA-AN-A046-01 COSM3816302 c.5534G>A p.R1845Q Substitution - Missense 15:51481572-51481572 - SNU-C4 COSM962698 c.8845G>A p.A2949T Substitution - Missense 15:51450185-51450185 - CPCG0183-P2 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - TCGA-HU-A4G9-01 COSM4055520 c.3363A>G p.Q1121Q Substitution - coding silent 15:51499861-51499861 - LIM1899 COSM4640005 c.7958C>T p.A2653V Substitution - Missense 15:51458761-51458761 - TCGA-EK-A3GK-01 COSM4854122 c.6919G>A p.E2307K Substitution - Missense 15:51476631-51476631 - T2197 COSM4678207 c.297C>T p.C99C Substitution - coding silent 15:51565155-51565155 - TCGA-DK-A3WW-01 COSM3794235 c.4790C>G p.S1597C Substitution - Missense 15:51491741-51491741 - ESCC_BICR_042T COSM5443667 c.855G>C p.E285D Substitution - Missense 15:51545658-51545658 - PT19_2 COSM5900301 c.4024C>T p.P1342S Substitution - Missense 15:51499200-51499200 - TCGA-CA-6717-01 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - ORL-48 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-BR-4191-01 COSM4055513 c.6700C>G p.L2234V Substitution - Missense 15:51480004-51480004 - TCGA-D1-A103-01 COSM962700 c.8631-1G>T p.? Unknown 15:51451698-51451698 - S02249 COSM5680006 c.4377G>T p.Q1459H Substitution - Missense 15:51498847-51498847 - TCGA-AA-A010-01 COSM280445 c.7135C>T p.R2379* Substitution - Nonsense 15:51474419-51474419 - PTC-77C COSM4128283 c.6717G>C p.Q2239H Substitution - Missense 15:51479987-51479987 - T2932 COSM4055512 c.7356C>T p.P2452P Substitution - coding silent 15:51471256-51471256 - TCGA-AX-A05Z-01 COSM962729 c.3261G>A p.K1087K Substitution - coding silent 15:51499963-51499963 - 587234 COSM1203894 c.2644+2T>C p.? Unknown 15:51514440-51514440 - EOPC-052_tumor_01 COSM5950921 c.6757G>T p.V2253L Substitution - Missense 15:51478347-51478347 - CRC-19T COSM5481253 c.3808G>T p.V1270L Substitution - Missense 15:51499416-51499416 - TCGA-B0-4852-01 COSM470793 c.591G>C p.W197C Substitution - Missense 15:51547385-51547385 - TCGA-EE-A2MS-06 COSM3502069 c.8750C>T p.S2917L Substitution - Missense 15:51450280-51450280 - PTC-515C COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - ML_97_T_01 COSM5038370 c.93T>C p.Y31Y Substitution - coding silent 15:51576176-51576176 - Pat_40_A COSM5849356 c.6154_6155delAT p.M2052fs*2 Deletion - Frameshift 15:51480951-51480952 - TCGA-AC-A2QH-01 COSM5832909 c.7176_7178delTGT p.V2393delV Deletion - In frame 15:51474376-51474378 - 090-05-01TD COSM145323 c.5770C>T p.P1924S Substitution - Missense 15:51481336-51481336 - 13681 COSM5614239 c.1297C>T p.H433Y Substitution - Missense 15:51538261-51538261 - TCGA-EK-A2PG-01 COSM4819772 c.5358C>T p.F1786F Substitution - coding silent 15:51486197-51486197 - TCGA-A8-A094-01 COSM434017 c.5218G>T p.V1740L Substitution - Missense 15:51486337-51486337 - TCGA-B0-4833-01 COSM3361442 c.6094G>T p.D2032Y Substitution - Missense 15:51481012-51481012 - Gp2D COSM4611732 c.5071_5072insA p.M1691fs*10 Insertion - Frameshift 15:51488099-51488100 - Malme-3M COSM1678459 c.7078C>T p.L2360F Substitution - Missense 15:51474476-51474476 - AOCS-158-1-6 COSM3981556 c.6078G>T p.E2026D Substitution - Missense 15:51481028-51481028 - 949_T COSM3956726 c.7822G>T p.A2608S Substitution - Missense 15:51463480-51463480 - D10 COSM5007064 c.6190G>A p.V2064I Substitution - Missense 15:51480916-51480916 - DN11153 COSM5769480 c.4252C>T p.R1418* Substitution - Nonsense 15:51498972-51498972 - Gp5D COSM4611732 c.5071_5072insA p.M1691fs*10 Insertion - Frameshift 15:51488099-51488100 - D28 COSM5544838 c.7352C>T p.P2451L Substitution - Missense 15:51471260-51471260 - TCGA-BS-A0UA-01 COSM962742 c.1234C>T p.R412* Substitution - Nonsense 15:51538324-51538324 - UM-SCC-17B COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-D1-A17Q-01 COSM962734 c.2451A>C p.E817D Substitution - Missense 15:51517153-51517153 - RK024_C COSM1629590 c.8568T>C p.S2856S Substitution - coding silent 15:51453612-51453612 - CSCC-37-T COSM4561274 c.8789G>A p.R2930K Substitution - Missense 15:51450241-51450241 - TCGA-D1-A16X-01 COSM280448 c.265A>C p.N89H Substitution - Missense 15:51568507-51568507 - TCGA-AR-A1AI-01 COSM434016 c.6966G>C p.V2322V Substitution - coding silent 15:51474588-51474588 - TCGA-B4-5836-01 COSM1493418 c.2216C>G p.T739S Substitution - Missense 15:51536264-51536264 - TCGA-AX-A05Z-01 COSM962740 c.1894T>C p.S632P Substitution - Missense 15:51536586-51536586 - CLL007 COSM1290397 c.2770G>A p.A924T Substitution - Missense 15:51503028-51503028 - YUDAB COSM1708175 c.4228G>A p.V1410I Substitution - Missense 15:51498996-51498996 - YURIDA COSM1708174 c.4600C>T p.L1534F Substitution - Missense 15:51498624-51498624 - UPCI:SCC090 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - 12T COSM106982 c.8855C>T p.P2952L Substitution - Missense 15:51450175-51450175 - ESO-081 COSM1243211 c.2651G>A p.R884H Substitution - Missense 15:51507247-51507247 - TCGA-AN-A0AK-01 COSM3816306 c.4729A>G p.T1577A Substitution - Missense 15:51495078-51495078 - 49M COSM5590567 c.577C>T p.L193F Substitution - Missense 15:51547399-51547399 - T578 COSM176027 c.4190G>A p.R1397Q Substitution - Missense 15:51499034-51499034 - TCGA-BW-A5NQ-01 COSM4911787 c.7781T>G p.L2594R Substitution - Missense 15:51464699-51464699 - TCGA-HE-7130-01 COSM3987999 c.5744C>T p.S1915F Substitution - Missense 15:51481362-51481362 - 49M COSM5590566 c.6685C>T p.H2229Y Substitution - Missense 15:51480019-51480019 - 090 COSM145323 c.5770C>T p.P1924S Substitution - Missense 15:51481336-51481336 - TCGA-B5-A0JY-01 COSM962746 c.442G>T p.E148* Substitution - Nonsense 15:51564183-51564183 - WSU-HN6 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - HCC053T COSM5803918 c.5032G>T p.V1678L Substitution - Missense 15:51488567-51488567 - HCC002T COSM5819373 c.7539A>T p.T2513T Substitution - coding silent 15:51465630-51465630 - 2492728 COSM5729705 c.7579C>T p.P2527S Substitution - Missense 15:51465590-51465590 - TCGA-59-2351-01 COSM70470 c.1746G>C p.E582D Substitution - Missense 15:51536734-51536734 - BN13 COSM1608469 c.6342A>G p.E2114E Substitution - coding silent 15:51480764-51480764 - HCC27 COSM3706618 c.8019T>C p.C2673C Substitution - coding silent 15:51458619-51458619 - CAL27 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-33-4566-01 COSM701063 c.7628G>T p.G2543V Substitution - Missense 15:51464852-51464852 - TCGA-AX-A05Z-01 COSM962700 c.8631-1G>T p.? Unknown 15:51451698-51451698 - BHY COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-DU-8165-01 COSM3969151 c.5624A>G p.D1875G Substitution - Missense 15:51481482-51481482 - 71 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - PD4937a COSM160468 c.564A>G p.G188G Substitution - coding silent 15:51563384-51563384 - TCGA-CD-A4MI-01 COSM4055523 c.1873G>A p.A625T Substitution - Missense 15:51536607-51536607 - TCGA-CA-6718-01 COSM1373418 c.6979A>C p.N2327H Substitution - Missense 15:51474575-51474575 - Au1 COSM343478 c.5384C>T p.P1795L Substitution - Missense 15:51486171-51486171 - TCGA-66-2773-01 COSM701059 c.1731G>T p.T577T Substitution - coding silent 15:51536749-51536749 - 090-02-1TD COSM145323 c.5770C>T p.P1924S Substitution - Missense 15:51481336-51481336 - TCGA-22-5471-01 COSM701054 c.741G>T p.M247I Substitution - Missense 15:51547235-51547235 - 6115247 COSM5571734 c.1918G>A p.V640I Substitution - Missense 15:51536562-51536562 - 3206A7_017_T COSM5041313 c.2969T>C p.V990A Substitution - Missense 15:51502829-51502829 - SJRHB011 COSM3737581 c.1498A>C p.T500P Substitution - Missense 15:51537607-51537607 - 07-057 COSM3736131 c.7121A>C p.H2374P Substitution - Missense 15:51474433-51474433 - HN_62426 COSM127816 c.6636T>C p.I2212I Substitution - coding silent 15:51480068-51480068 - LUAD-S01357 COSM386677 c.2921C>G p.S974C Substitution - Missense 15:51502877-51502877 - Pat_76_A COSM5849357 c.5183delT p.F1728fs*3 Deletion - Frameshift 15:51487988-51487988 - PTC-28C COSM4128285 c.2881A>C p.I961L Substitution - Missense 15:51502917-51502917 - TCGA-FS-A1ZZ-06 COSM3502089 c.4279C>T p.P1427S Substitution - Missense 15:51498945-51498945 - TCGA-AP-A051-01 COSM962701 c.8485T>G p.F2829V Substitution - Missense 15:51455204-51455204 - TCGA-CC-A3MA-01 COSM4942842 c.8330A>G p.Y2777C Substitution - Missense 15:51456311-51456311 - CPCG0184-P2 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - TCGA-AP-A059-01 COSM962728 c.3471G>T p.K1157N Substitution - Missense 15:51499753-51499753 - WSU-HN12 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - 2521243 COSM5886874 c.8660C>T p.S2887L Substitution - Missense 15:51451668-51451668 - GC8_T COSM147909 c.2823C>T p.N941N Substitution - coding silent 15:51502975-51502975 - TCGA-FW-A3R5-06 COSM3887126 c.697C>T p.R233* Substitution - Nonsense 15:51547279-51547279 - PT45 COSM1708176 c.716C>T p.S239L Substitution - Missense 15:51547260-51547260 - RMS110_ COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AP-A051-01 COSM962735 c.2264C>T p.A755V Substitution - Missense 15:51536216-51536216 - RK298_C01 COSM3700975 c.4783+4A>C p.? Unknown 15:51495020-51495020 - TCGA-G9-6342-01 COSM3672070 c.803G>T p.W268L Substitution - Missense 15:51545710-51545710 - PD7307a COSM5800354 c.8618C>T p.S2873F Substitution - Missense 15:51453562-51453562 - TCGA-AP-A051-01 COSM962727 c.3561C>T p.V1187V Substitution - coding silent 15:51499663-51499663 - PD8997a COSM5769480 c.4252C>T p.R1418* Substitution - Nonsense 15:51498972-51498972 - CSCC-31-T COSM4495781 c.460C>T p.P154S Substitution - Missense 15:51564165-51564165 - PTC-28C COSM4128286 c.2877A>T p.S959S Substitution - coding silent 15:51502921-51502921 - MO_1013 COSM5556327 c.5089C>A p.H1697N Substitution - Missense 15:51488082-51488082 - CSCC-62-T COSM4489046 c.3423C>T p.V1141V Substitution - coding silent 15:51499801-51499801 - BICR_22 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-G2-A2EO-01 COSM1301215 c.6340G>A p.E2114K Substitution - Missense 15:51480766-51480766 - TCGA-EE-A2MI-06 COSM3502104 c.353G>A p.W118* Substitution - Nonsense 15:51565099-51565099 - B112-Tumor COSM3932113 c.3860G>T p.S1287I Substitution - Missense 15:51499364-51499364 - TCGA-DW-5560-01 COSM3988000 c.4820C>T p.S1607F Substitution - Missense 15:51491711-51491711 - CSCC-55-T COSM4569858 c.2103T>C p.G701G Substitution - coding silent 15:51536377-51536377 - pfg144T COSM4755170 c.6031G>C p.D2011H Substitution - Missense 15:51481075-51481075 - TCGA-FR-A3R1-01 COSM3502085 c.5141C>T p.S1714F Substitution - Missense 15:51488030-51488030 - TCGA-DS-A0VN-01 COSM459008 c.7838G>A p.R2613Q Substitution - Missense 15:51463464-51463464 - 3N57-VS-3T57 COSM4983936 c.2072G>A p.R691K Substitution - Missense 15:51536408-51536408 - TCGA-AP-A0LM-01 COSM962714 c.5429G>A p.R1810Q Substitution - Missense 15:51486126-51486126 - TCGA-BS-A0UV-01 COSM962742 c.1234C>T p.R412* Substitution - Nonsense 15:51538324-51538324 - 46M COSM5587640 c.4536G>A p.R1512R Substitution - coding silent 15:51498688-51498688 - HCC021T COSM5815816 c.6233A>T p.E2078V Substitution - Missense 15:51480873-51480873 - TCGA-AP-A059-01 COSM962707 c.7061G>A p.S2354N Substitution - Missense 15:51474493-51474493 - CSCC-31-T COSM4486435 c.3053C>T p.T1018I Substitution - Missense 15:51500171-51500171 - YUDAB COSM1708176 c.716C>T p.S239L Substitution - Missense 15:51547260-51547260 - PTC-14C COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - OSCC-GB_01350111 COSM5955894 c.7748C>T p.A2583V Substitution - Missense 15:51464732-51464732 - TCGA-LP-A7HU-01 COSM4825765 c.332C>T p.S111F Substitution - Missense 15:51565120-51565120 - TCGA-GL-7773-01 COSM3988001 c.4671A>C p.S1557S Substitution - coding silent 15:51498553-51498553 - TCGA-D3-A2JF-06 COSM3502102 c.777A>T p.S259S Substitution - coding silent 15:51545736-51545736 - TCGA-AX-A0J1-01 COSM962715 c.5428C>T p.R1810* Substitution - Nonsense 15:51486127-51486127 - I2L-P19Ta-Tumor-Organoid COSM5362912 c.4255G>T p.D1419Y Substitution - Missense 15:51498969-51498969 - CSCC-56-T COSM4496589 c.4788C>A p.V1596V Substitution - coding silent 15:51491743-51491743 - CRC-02T COSM5454359 c.5639T>C p.I1880T Substitution - Missense 15:51481467-51481467 - TCGA-29-1696-01 COSM1323950 c.1618-1G>T p.? Unknown 15:51536863-51536863 - HCT-15 COSM1678462 c.4405T>C p.S1469P Substitution - Missense 15:51498819-51498819 - TCGA-CC-5259-01 COSM4928227 c.1875A>T p.A625A Substitution - coding silent 15:51536605-51536605 - TCGA-G9-6378-01 COSM1129180 c.2992+1G>A p.? Unknown 15:51502805-51502805 - 587376 COSM1203896 c.2486G>A p.R829Q Substitution - Missense 15:51517118-51517118 - 39 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - BRC39 COSM5027974 c.2240G>C p.R747P Substitution - Missense 15:51536240-51536240 - TCGA-F5-6814-01 COSM3420410 c.1572G>T p.V524V Substitution - coding silent 15:51537533-51537533 - TCGA-BR-8363-01 COSM4055526 c.899G>A p.R300K Substitution - Missense 15:51545614-51545614 - TCGA-DS-A1OC-01 COSM1293536 c.1798A>C p.S600R Substitution - Missense 15:51536682-51536682 - TCGA-CG-4305-01 COSM4055524 c.1612G>C p.V538L Substitution - Missense 15:51537493-51537493 - RK140_C01 COSM3700976 c.3553G>A p.V1185M Substitution - Missense 15:51499671-51499671 - TCGA-GF-A6C9-06 COSM4903687 c.1765C>T p.P589S Substitution - Missense 15:51536715-51536715 - TCGA-EJ-5532-01 COSM1129179 c.531G>A p.W177* Substitution - Nonsense 15:51563417-51563417 - TCGA-AA-A010-01 COSM280446 c.3295G>T p.E1099* Substitution - Nonsense 15:51499929-51499929 - TCGA-RP-A693-06 COSM4895898 c.7091C>T p.S2364F Substitution - Missense 15:51474463-51474463 - TCGA-FW-A3R5-06 COSM3887124 c.3155C>T p.P1052L Substitution - Missense 15:51500069-51500069 - PCSI_0325_Pa_P_526 COSM4809200 c.1941C>T p.C647C Substitution - coding silent 15:51536539-51536539 - TCGA-DM-A1DB-01 COSM5828247 c.88-3delT p.? Unknown 15:51576184-51576184 - T3091 COSM2216936 c.8756_8757insG p.R2920fs*1 Insertion - Frameshift 15:51450273-51450274 - TCGA-04-1343-01 COSM74387 c.2345T>C p.F782S Substitution - Missense 15:51535754-51535754 - HT115 COSM555593 c.8971C>T p.R2991* Substitution - Nonsense 15:51449124-51449124 - CLL024 COSM1290396 c.6580C>A p.Q2194K Substitution - Missense 15:51480124-51480124 - TCGA-BR-8680-01 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - CHC892T COSM4798316 c.1618-1G>A p.? Unknown 15:51536863-51536863 - YUFERY COSM5383482 c.7766G>A p.R2589Q Substitution - Missense 15:51464714-51464714 - TCGA-AZ-6601-01 COSM1373438 c.1463C>T p.T488M Substitution - Missense 15:51537642-51537642 - RMS106_ COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - RK043_C01 COSM3700974 c.5688A>G p.G1896G Substitution - coding silent 15:51481418-51481418 - PR-01-2492 COSM244066 c.4659T>C p.D1553D Substitution - coding silent 15:51498565-51498565 - TCGA-AP-A056-01 COSM280446 c.3295G>T p.E1099* Substitution - Nonsense 15:51499929-51499929 - HT55 COSM2216969 c.7052T>C p.V2351A Substitution - Missense 15:51474502-51474502 - TCGA-GN-A269-01 COSM3502101 c.1160G>A p.G387D Substitution - Missense 15:51538398-51538398 - TCGA-EE-A2MR-06 COSM3502079 c.6437C>T p.S2146L Substitution - Missense 15:51480669-51480669 - 134 COSM3732932 c.3492_3493insC p.I1165fs*39 Insertion - Frameshift 15:51499731-51499732 - TCGA-HU-8243-01 COSM4055507 c.8799G>A p.Q2933Q Substitution - coding silent 15:51450231-51450231 - TCGA-BR-8589-01 COSM4055514 c.6311A>G p.K2104R Substitution - Missense 15:51480795-51480795 - UM-SCC-2 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-DK-A3IT-01 COSM1301211 c.7435G>A p.E2479K Substitution - Missense 15:51466266-51466266 - TCGA-HR-A2OG-01 COSM3502091 c.3373C>T p.L1125F Substitution - Missense 15:51499851-51499851 - TCGA-AX-A0J0-01 COSM962697 c.9097C>A p.L3033I Substitution - Missense 15:51448998-51448998 - TCGA-G2-A2EO-01 COSM1301214 c.6395G>C p.R2132T Substitution - Missense 15:51480711-51480711 - TCGA-G2-A3IB-01 COSM1301210 c.9090C>A p.N3030K Substitution - Missense 15:51449005-51449005 - SCC-15 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - CHC892T COSM4958558 c.5051G>A p.R1684K Substitution - Missense 15:51488548-51488548 - TCGA-E9-A3QA-01 COSM3816305 c.4993G>C p.D1665H Substitution - Missense 15:51488606-51488606 - HCC066T COSM5821534 c.3645T>C p.T1215T Substitution - coding silent 15:51499579-51499579 - PDA_060 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - NCI-H720 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - T3336 COSM4678204 c.5158C>T p.R1720C Substitution - Missense 15:51488013-51488013 - DN11190 COSM5800354 c.8618C>T p.S2873F Substitution - Missense 15:51453562-51453562 - Pat_36_B COSM5849358 c.2836C>T p.P946S Substitution - Missense 15:51502962-51502962 - S02292 COSM5687473 c.1320G>T p.R440R Substitution - coding silent 15:51538238-51538238 - OSCC-GB_01310111 COSM5954263 c.4482A>T p.K1494N Substitution - Missense 15:51498742-51498742 - HT115 COSM2216948 c.8122G>T p.E2708* Substitution - Nonsense 15:51458516-51458516 - CSCC-7-T COSM4570599 c.295T>G p.C99G Substitution - Missense 15:51565157-51565157 - TCGA-B5-A11E-01 COSM962712 c.6261A>G p.I2087M Substitution - Missense 15:51480845-51480845 - LIM1215 COSM4639398 c.376T>G p.L126V Substitution - Missense 15:51564249-51564249 - TCGA-ER-A19E-06 COSM3502077 c.7245C>T p.H2415H Substitution - coding silent 15:51471367-51471367 - CPCG0249-F1 COSM4879987 c.5392C>T p.R1798C Substitution - Missense 15:51486163-51486163 - TCGA-66-2785-01 COSM701060 c.1998G>C p.L666F Substitution - Missense 15:51536482-51536482 - 587228 COSM1203889 c.3562G>A p.G1188S Substitution - Missense 15:51499662-51499662 - TCGA-AP-A051-01 COSM962713 c.5493G>A p.K1831K Substitution - coding silent 15:51481613-51481613 - UM-SCC-2 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - RKO COSM2216961 c.7533T>C p.H2511H Substitution - coding silent 15:51465636-51465636 - 49 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - TCGA-B5-A11E-01 COSM962745 c.686T>C p.L229S Substitution - Missense 15:51547290-51547290 - TCGA-AN-A046-01 COSM3816304 c.5230A>C p.K1744Q Substitution - Missense 15:51486325-51486325 - BN13T COSM1608469 c.6342A>G p.E2114E Substitution - coding silent 15:51480764-51480764 - TCGA-AP-A0LM-01 COSM962749 c.367A>G p.N123D Substitution - Missense 15:51564258-51564258 - TCGA-D5-6928-01 COSM1373430 c.2512G>A p.A838T Substitution - Missense 15:51517092-51517092 - Au4 COSM5603379 c.2663T>A p.F888Y Substitution - Missense 15:51507235-51507235 - TCGA-EE-A29E-06 COSM3502094 c.2848C>T p.P950S Substitution - Missense 15:51502950-51502950 - 587238 COSM1203888 c.7986G>A p.M2662I Substitution - Missense 15:51458733-51458733 - CSB17 COSM5027975 c.1106-1G>T p.? Unknown 15:51538453-51538453 - 2 COSM4172184 c.7114_7125del12 p.A2372_P2375delAAHP Deletion - In frame 15:51474429-51474440 - TCGA-BR-4361-01 COSM4055527 c.497G>A p.C166Y Substitution - Missense 15:51564128-51564128 - SCC-25 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - PT28 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - 55 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - C658 COSM4443279 c.6706A>G p.T2236A Substitution - Missense 15:51479998-51479998 - SC_9055 COSM4055525 c.1318C>T p.R440W Substitution - Missense 15:51538240-51538240 - TCGA-BR-4361-01 COSM4055525 c.1318C>T p.R440W Substitution - Missense 15:51538240-51538240 - NOKSI COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - PD4115a COSM3664756 c.7518-1G>A p.? Unknown 15:51465652-51465652 - TCGA-BT-A2LB-01 COSM3794236 c.3701G>C p.R1234T Substitution - Missense 15:51499523-51499523 - PTC-46C COSM4128289 c.88G>T p.A30S Substitution - Missense 15:51576181-51576181 - TCGA-AP-A0LM-01 COSM962747 c.440A>C p.E147A Substitution - Missense 15:51564185-51564185 - TCGA-BR-6452-01 COSM4055522 c.1935A>T p.R645S Substitution - Missense 15:51536545-51536545 - TCGA-B5-A0JY-01 COSM962722 c.4495T>G p.S1499A Substitution - Missense 15:51498729-51498729 - TCGA-CK-5916-01 COSM1373416 c.7155delT p.F2385fs*5 Deletion - Frameshift 15:51474399-51474399 - TCGA-DA-A1I7-06 COSM3502096 c.2146C>T p.H716Y Substitution - Missense 15:51536334-51536334 - PD4115a COSM3664756 c.7518-1G>A p.? Unknown 15:51465652-51465652 - TCGA-BS-A0UA-01 COSM962704 c.7218T>C p.P2406P Substitution - coding silent 15:51471394-51471394 - HCC35 COSM1608472 c.128A>G p.D43G Substitution - Missense 15:51576141-51576141 - pfg068T COSM4765772 c.5072_5073insA p.M1691fs*10 Insertion - Frameshift 15:51488098-51488099 - WSU-HN8 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - UM-SCC-4 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-AA-A00N-01 COSM274808 c.7046T>C p.V2349A Substitution - Missense 15:51474508-51474508 - PTC-28C COSM4128284 c.2884G>A p.A962T Substitution - Missense 15:51502914-51502914 - PD9464a COSM5792472 c.796C>T p.R266W Substitution - Missense 15:51545717-51545717 - ORL-48 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - CPCG0184-P4 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - SA054 COSM213079 c.8153G>A p.R2718H Substitution - Missense 15:51457446-51457446 - TCGA-AA-A010-01 COSM280444 c.8072C>A p.S2691Y Substitution - Missense 15:51458566-51458566 - BD55T COSM5509504 c.3704C>G p.S1235C Substitution - Missense 15:51499520-51499520 - SMS-CTR COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - RK261_C01 COSM4778291 c.3623A>C p.K1208T Substitution - Missense 15:51499601-51499601 - HN_62506 COSM126657 c.2730G>A p.W910* Substitution - Nonsense 15:51507168-51507168 - C135 COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - BD55T COSM5509505 c.3647T>C p.L1216S Substitution - Missense 15:51499577-51499577 - YUHEF COSM1708177 c.143A>T p.Q48L Substitution - Missense 15:51576126-51576126 - TCGA-29-1710-01 COSM1323953 c.8811G>A p.T2937T Substitution - coding silent 15:51450219-51450219 - HCT-116 COSM1678458 c.8788A>G p.R2930G Substitution - Missense 15:51450242-51450242 - TCGA-F5-6814-01 COSM3420409 c.2249C>A p.S750Y Substitution - Missense 15:51536231-51536231 - TCGA-AP-A056-01 COSM962748 c.372A>C p.R124S Substitution - Missense 15:51564253-51564253 - RMS77_ COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - Pat_14_A COSM5849355 c.7400C>T p.P2467L Substitution - Missense 15:51466301-51466301 - B86-Tumor COSM1749204 c.6565G>A p.E2189K Substitution - Missense 15:51480139-51480139 - TCGA-EE-A2GO-06 COSM3502069 c.8750C>T p.S2917L Substitution - Missense 15:51450280-51450280 - ESCC_92 COSM213079 c.8153G>A p.R2718H Substitution - Missense 15:51457446-51457446 - ESCC-F43 COSM5047799 c.2270C>G p.S757C Substitution - Missense 15:51536210-51536210 - Gp2D COSM2216988 c.5605delA p.T1869fs*12 Deletion - Frameshift 15:51481501-51481501 - TCGA-AP-A0LM-01 COSM962720 c.4678G>T p.D1560Y Substitution - Missense 15:51495129-51495129 - S02402 COSM5700167 c.721C>T p.R241C Substitution - Missense 15:51547255-51547255 - PD4120a COSM160467 c.5127G>C p.L1709F Substitution - Missense 15:51488044-51488044 - TCGA-DM-A28K-01 COSM1373414 c.8175T>C p.Y2725Y Substitution - coding silent 15:51457424-51457424 - T578 COSM2216940 c.8404C>T p.R2802C Substitution - Missense 15:51456122-51456122 - TCGA-CM-6674-01 COSM1373420 c.5084delT p.F1695fs*15 Deletion - Frameshift 15:51488087-51488087 - 49 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - TCGA-BT-A3PJ-01 COSM3794237 c.3701G>A p.R1234K Substitution - Missense 15:51499523-51499523 - sysucc-1024T COSM4640005 c.7958C>T p.A2653V Substitution - Missense 15:51458761-51458761 - 228 COSM4426080 c.2315G>A p.G772D Substitution - Missense 15:51535784-51535784 - TCGA-EE-A3AB-06 COSM3502087 c.4502A>G p.Y1501C Substitution - Missense 15:51498722-51498722 - HT115 COSM2216990 c.5558G>T p.R1853I Substitution - Missense 15:51481548-51481548 - TCGA-D3-A2JC-06 COSM3502078 c.6531G>A p.M2177I Substitution - Missense 15:51480575-51480575 - TCGA-HU-A4GU-01 COSM1243211 c.2651G>A p.R884H Substitution - Missense 15:51507247-51507247 - 84 COSM3732831 c.3488C>A p.P1163Q Substitution - Missense 15:51499736-51499736 - T3021 COSM4678206 c.4749G>A p.L1583L Substitution - coding silent 15:51495058-51495058 - HCC058T COSM5804966 c.8720A>T p.Q2907L Substitution - Missense 15:51450310-51450310 - TCGA-AP-A0LM-01 COSM962725 c.4028C>A p.T1343N Substitution - Missense 15:51499196-51499196 - MD-127 COSM302069 c.7491G>A p.Q2497Q Substitution - coding silent 15:51466210-51466210 - Pat_60_B COSM5849359 c.1820_1836del17 p.A607fs*3 Deletion - Frameshift 15:51536644-51536660 - TCGA-EE-A2GJ-06 COSM3502083 c.5691C>T p.C1897C Substitution - coding silent 15:51481415-51481415 - TCGA-22-4613-01 COSM701064 c.7868T>C p.V2623A Substitution - Missense 15:51463434-51463434 - 391 COSM3721507 c.6638C>T p.A2213V Substitution - Missense 15:51480066-51480066 - SCC-25 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-56-1622-01 COSM701058 c.1678A>G p.K560E Substitution - Missense 15:51536802-51536802 - T3454 COSM4678201 c.8380C>T p.R2794W Substitution - Missense 15:51456146-51456146 - KYSE110 COSM5049497 c.3011C>T p.S1004L Substitution - Missense 15:51500213-51500213 - TCGA-GF-A3OT-06 COSM3502103 c.595C>T p.P199S Substitution - Missense 15:51547381-51547381 - PT36 COSM5916419 c.3896C>T p.S1299L Substitution - Missense 15:51499328-51499328 - 68 COSM5012883 c.1865A>G p.N622S Substitution - Missense 15:51536615-51536615 - TCGA-F5-6814-01 COSM3420411 c.650G>T p.R217M Substitution - Missense 15:51547326-51547326 - TCGA-EE-A29M-06 COSM3502068 c.8963C>T p.S2988F Substitution - Missense 15:51449132-51449132 - AOCS-139-19-0 COSM3981557 c.4993G>A p.D1665N Substitution - Missense 15:51488606-51488606 - TCGA-AQ-A54O-01 COSM5832910 c.4966delT p.S1656fs*9 Deletion - Frameshift 15:51488633-51488633 - TCGA-FS-A4FC-06 COSM3502084 c.5383C>T p.P1795S Substitution - Missense 15:51486172-51486172 - 9 COSM4166956 c.2354C>G p.S785C Substitution - Missense 15:51535745-51535745 - TCGA-AA-A00N-01 COSM298641 c.4839G>T p.L1613L Substitution - coding silent 15:51491692-51491692 - 749-02-16TD COSM701064 c.7868T>C p.V2623A Substitution - Missense 15:51463434-51463434 - TCGA-D1-A15X-01 COSM962711 c.6313G>A p.V2105I Substitution - Missense 15:51480793-51480793 - TCGA-GF-A6C9-06 COSM4901937 c.3953C>T p.S1318F Substitution - Missense 15:51499271-51499271 - 587342 COSM1203892 c.8381G>A p.R2794Q Substitution - Missense 15:51456145-51456145 - S02273 COSM5681647 c.4288C>T p.P1430S Substitution - Missense 15:51498936-51498936 - TCGA-EE-A3JD-06 COSM4393862 c.8926C>T p.L2976L Substitution - coding silent 15:51449169-51449169 - 1N37-VS-1T37 COSM4975015 c.1710G>A p.A570A Substitution - coding silent 15:51536770-51536770 - LUAD-NYU160 COSM370438 c.1771G>C p.G591R Substitution - Missense 15:51536709-51536709 - Gp5D COSM2216988 c.5605delA p.T1869fs*12 Deletion - Frameshift 15:51481501-51481501 - PET052T COSM5824778 c.8000C>A p.S2667Y Substitution - Missense 15:51458719-51458719 - TCGA-CG-5721-01 COSM4055521 c.2416T>C p.L806L Substitution - coding silent 15:51535683-51535683 - 19 COSM5747645 c.7480A>G p.T2494A Substitution - Missense 15:51466221-51466221 - TCGA-A2-A04T-01 COSM3816311 c.1756G>C p.V586L Substitution - Missense 15:51536724-51536724 - TCGA-37-4141-01 COSM701065 c.8087A>T p.Q2696L Substitution - Missense 15:51458551-51458551 - RK024_C01 COSM1629590 c.8568T>C p.S2856S Substitution - coding silent 15:51453612-51453612 - TCGA-BR-A4CQ-01 COSM4055512 c.7356C>T p.P2452P Substitution - coding silent 15:51471256-51471256 - TCGA-AN-A046-01 COSM3816309 c.2676C>A p.F892L Substitution - Missense 15:51507222-51507222 - SNU-C2B COSM2217077 c.385A>G p.T129A Substitution - Missense 15:51564240-51564240 - TCGA-AA-3713-01 COSM1373428 c.2731C>T p.H911Y Substitution - Missense 15:51507167-51507167 - TCGA-HG-A2PA-01 COSM4823661 c.8327A>G p.Q2776R Substitution - Missense 15:51456314-51456314 - TCGA-29-1768-01 COSM1323954 c.8912T>G p.L2971W Substitution - Missense 15:51449183-51449183 - T3080 COSM2217027 c.2982G>A p.T994T Substitution - coding silent 15:51502816-51502816 - TCGA-AN-A046-01 COSM3816308 c.3384G>T p.L1128F Substitution - Missense 15:51499840-51499840 - 1255_T COSM3956728 c.2038G>T p.D680Y Substitution - Missense 15:51536442-51536442 - CCK81 COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - TCGA-13-2071-01 COSM1323952 c.5855G>A p.W1952* Substitution - Nonsense 15:51481251-51481251 - CHC892T COSM4958558 c.5051G>A p.R1684K Substitution - Missense 15:51488548-51488548 - TCGA-FS-A4FC-06 COSM3502073 c.7593G>A p.L2531L Substitution - coding silent 15:51465576-51465576 - PTC-28C COSM4128287 c.2875T>A p.S959T Substitution - Missense 15:51502923-51502923 - CRC-06T COSM5456487 c.8684-2A>G p.? Unknown 15:51450348-51450348 - TCGA-BT-A20N-01 COSM416904 c.5737A>G p.K1913E Substitution - Missense 15:51481369-51481369 - TCGA-FW-A3R5-06 COSM3887125 c.2846C>T p.S949F Substitution - Missense 15:51502952-51502952 - TCGA-JX-A3Q0-01 COSM4824878 c.8326C>G p.Q2776E Substitution - Missense 15:51456315-51456315 - TCGA-BS-A0UV-01 COSM962744 c.949A>T p.N317Y Substitution - Missense 15:51542489-51542489 - PT46 COSM5929563 c.4247G>A p.G1416D Substitution - Missense 15:51498977-51498977 - TCGA-24-1563-01 COSM81097 c.1455A>C p.P485P Substitution - coding silent 15:51537650-51537650 - TCGA-B5-A0JY-01 COSM962733 c.2890C>A p.L964I Substitution - Missense 15:51502908-51502908 - TCGA-A7-A5ZV-01 COSM3816298 c.7736T>A p.L2579H Substitution - Missense 15:51464744-51464744 - Case5 COSM1579482 c.4093A>G p.K1365E Substitution - Missense 15:51499131-51499131 - TCGA-G2-A2EO-01 COSM1301217 c.5929G>C p.D1977H Substitution - Missense 15:51481177-51481177 - LUAD-YINHD COSM349050 c.7099G>A p.E2367K Substitution - Missense 15:51474455-51474455 - TCGA-F5-6814-01 COSM3420406 c.6681T>G p.N2227K Substitution - Missense 15:51480023-51480023 - TCGA-AA-A00N-01 COSM274810 c.4926T>G p.I1642M Substitution - Missense 15:51491605-51491605 - 234 COSM3731158 c.2186G>A p.R729H Substitution - Missense 15:51536294-51536294 - TCGA-CK-5916-01 COSM5828248 c.88-6_88-3delTTTT p.? Unknown 15:51576184-51576187 - TCGA-B5-A0JY-01 COSM962743 c.982C>A p.L328I Substitution - Missense 15:51542456-51542456 - TCGA-EE-A2MD-06 COSM3502098 c.1352C>T p.S451F Substitution - Missense 15:51537753-51537753 - PTC-28C COSM4128290 c.81C>T p.P27P Substitution - coding silent 15:51622465-51622465 - ESCC_143 COSM5644086 c.8757_8758insG p.R2920fs*9 Insertion - Frameshift 15:51450272-51450273 - T3080 COSM4678203 c.5788A>G p.R1930G Substitution - Missense 15:51481318-51481318 - TCGA-BS-A0UV-01 COSM962738 c.2146C>A p.H716N Substitution - Missense 15:51536334-51536334 - TCGA-AC-A23H-01 COSM3816299 c.6415G>C p.E2139Q Substitution - Missense 15:51480691-51480691 - C391 COSM4441643 c.8353G>A p.G2785S Substitution - Missense 15:51456173-51456173 - HCC126 COSM3706619 c.4748T>A p.L1583Q Substitution - Missense 15:51495059-51495059 - 126T COSM1725606 c.8011-1G>A p.? Unknown 15:51458628-51458628 - GC8_T COSM147907 c.4908A>G p.G1636G Substitution - coding silent 15:51491623-51491623 - 721LT COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - TCGA-D1-A17Q-01 COSM701061 c.3376G>A p.D1126N Substitution - Missense 15:51499848-51499848 - UPCI:SCC090 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-AO-A128-01 COSM5832911 c.4653delC p.S1551fs*12 Deletion - Frameshift 15:51498571-51498571 - TCGA-ER-A19H-06 COSM3502075 c.7477G>A p.D2493N Substitution - Missense 15:51466224-51466224 - T1154 COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - ESCC_82 COSM5636044 c.8461-2A>G p.? Unknown 15:51455230-51455230 - SNUH_G16_S1 COSM3999555 c.4908A>T p.G1636G Substitution - coding silent 15:51491623-51491623 - SNUH_G15_S1 COSM3678223 c.5932T>G p.W1978G Substitution - Missense 15:51481174-51481174 - TCGA-EE-A2GJ-06 COSM176027 c.4190G>A p.R1397Q Substitution - Missense 15:51499034-51499034 - HCT15 COSM1678462 c.4405T>C p.S1469P Substitution - Missense 15:51498819-51498819 - CHEWS006 COSM4578325 c.1436G>A p.R479Q Substitution - Missense 15:51537669-51537669 - TCGA-ER-A193-06 COSM3502095 c.2813G>T p.G938V Substitution - Missense 15:51502985-51502985 - RK268_C01 COSM4945424 c.3989A>G p.D1330G Substitution - Missense 15:51499235-51499235 - GCT27 COSM5749550 c.6553G>A p.E2185K Substitution - Missense 15:51480553-51480553 - PTC-515C COSM4128290 c.81C>T p.P27P Substitution - coding silent 15:51622465-51622465 - TCGA-24-1567-01 COSM77589 c.3570T>A p.N1190K Substitution - Missense 15:51499654-51499654 - CHC892T COSM4798316 c.1618-1G>A p.? Unknown 15:51536863-51536863 - 49M COSM5590568 c.7092C>T p.S2364S Substitution - coding silent 15:51474462-51474462 - TCGA-B0-4852-01 COSM470787 c.8927T>C p.L2976P Substitution - Missense 15:51449168-51449168 - TCGA-CZ-4861-01 COSM3361443 c.4621G>T p.V1541L Substitution - Missense 15:51498603-51498603 - PT37 COSM5920807 c.8384C>T p.P2795L Substitution - Missense 15:51456142-51456142 - TCGA-F5-6814-01 COSM3420412 c.281A>C p.N94T Substitution - Missense 15:51568491-51568491 - TCGA-AO-A128-01 COSM5832912 c.4647_4648delTG p.D1549fs*5 Deletion - Frameshift 15:51498576-51498577 - SJRHB011_D COSM3737581 c.1498A>C p.T500P Substitution - Missense 15:51537607-51537607 - TCGA-BR-4191-01 COSM4055518 c.4609T>A p.L1537M Substitution - Missense 15:51498615-51498615 - SNUH_G16_S1 COSM147909 c.2823C>T p.N941N Substitution - coding silent 15:51502975-51502975 - CSCC-27-T COSM4475301 c.1979C>T p.S660L Substitution - Missense 15:51536501-51536501 - LS411 COSM2216973 c.6598C>A p.P2200T Substitution - Missense 15:51480106-51480106 - LS411 COSM2217004 c.4895C>T p.A1632V Substitution - Missense 15:51491636-51491636 - HCC27T COSM3706618 c.8019T>C p.C2673C Substitution - coding silent 15:51458619-51458619 - 74 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - pfg068T COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - TCGA-ER-A193-06 COSM3887123 c.7208C>T p.S2403L Substitution - Missense 15:51474346-51474346 - HCT116 COSM1678458 c.8788A>G p.R2930G Substitution - Missense 15:51450242-51450242 - PT35 COSM5913658 c.118T>A p.L40M Substitution - Missense 15:51576151-51576151 - JEKO-1 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - UM-SCC-4 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AP-A059-01 COSM962705 c.7186C>T p.R2396* Substitution - Nonsense 15:51474368-51474368 - HX33T COSM3706618 c.8019T>C p.C2673C Substitution - coding silent 15:51458619-51458619 - 1N57-VS-1T57 COSM4977346 c.5579G>A p.G1860E Substitution - Missense 15:51481527-51481527 - CAL33 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - PD4115a COSM3664756 c.7518-1G>A p.? Unknown 15:51465652-51465652 - TCGA-BR-7707-01 COSM4055516 c.5530C>A p.L1844I Substitution - Missense 15:51481576-51481576 - TCGA-EW-A1P4-01 COSM1478184 c.6024A>G p.K2008K Substitution - coding silent 15:51481082-51481082 - TCGA-CA-6718-01 COSM1373427 c.2820G>T p.K940N Substitution - Missense 15:51502978-51502978 - HCC35T COSM1608472 c.128A>G p.D43G Substitution - Missense 15:51576141-51576141 - TCGA-B0-5709-01 COSM470789 c.5294C>A p.S1765* Substitution - Nonsense 15:51486261-51486261 - C086 COSM1708176 c.716C>T p.S239L Substitution - Missense 15:51547260-51547260 - CPCG0184-P1 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - Pat_16_A COSM1373415 c.7474delT p.S2492fs*21 Deletion - Frameshift 15:51466227-51466227 - CSCC-31-T COSM4508707 c.7852C>T p.L2618F Substitution - Missense 15:51463450-51463450 - ESO-555 COSM1250295 c.3315T>A p.C1105* Substitution - Nonsense 15:51499909-51499909 - HDC87 COSM4636928 c.1820C>T p.A607V Substitution - Missense 15:51536660-51536660 - TCGA-BS-A0UV-01 COSM962721 c.4662G>T p.K1554N Substitution - Missense 15:51498562-51498562 - TCGA-BT-A3PK-01 COSM3794238 c.3078C>G p.F1026L Substitution - Missense 15:51500146-51500146 - CSCC-49-T COSM4550517 c.5022G>A p.K1674K Substitution - coding silent 15:51488577-51488577 - TCGA-BS-A0UJ-01 COSM962717 c.4967C>A p.S1656Y Substitution - Missense 15:51488632-51488632 - 39 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - 05-P8014 COSM4578324 c.5763delA p.D1922fs*20 Deletion - Frameshift 15:51481343-51481343 - UD-SCC-2 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - PAPNNX COSM5004648 c.6438G>A p.S2146S Substitution - coding silent 15:51480668-51480668 - SC_9096 COSM5556666 c.1770C>T p.H590H Substitution - coding silent 15:51536710-51536710 - RKO COSM4647823 c.7329A>G p.P2443P Substitution - coding silent 15:51471283-51471283 - NCI-H322M COSM1678463 c.110T>C p.I37T Substitution - Missense 15:51576159-51576159 - CPCG_0184_Pr_P_P2 COSM2217013 c.4144G>A p.V1382I Substitution - Missense 15:51499080-51499080 - CSCC-29-T COSM4561587 c.8902G>A p.V2968I Substitution - Missense 15:51449193-51449193 - TCGA-B5-A11Y-01 COSM962750 c.187G>T p.V63L Substitution - Missense 15:51576082-51576082 - Patient_1 COSM5414120 c.6961G>C p.G2321R Substitution - Missense 15:51476589-51476589 - 4095_T COSM3956727 c.3093G>T p.M1031I Substitution - Missense 15:51500131-51500131 - SCC-15 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AC-A2B8-01 COSM3816313 c.291C>G p.L97L Substitution - coding silent 15:51565161-51565161 - SNU-C4 COSM4652608 c.2265G>A p.A755A Substitution - coding silent 15:51536215-51536215 - HCC17 COSM1608468 c.8972G>A p.R2991Q Substitution - Missense 15:51449123-51449123 - CSCC-31-T COSM4508679 c.7840C>T p.L2614F Substitution - Missense 15:51463462-51463462 - 8066738 COSM3769607 c.2315-3C>T p.? Unknown 15:51535787-51535787 - TCGA-AX-A0J0-01 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - TCGA-D1-A16X-01 COSM962739 c.2063A>C p.K688T Substitution - Missense 15:51536417-51536417 - CHEWS007 COSM4578323 c.9071A>G p.N3024S Substitution - Missense 15:51449024-51449024 - TCGA-AP-A059-01 COSM962723 c.4436C>T p.T1479M Substitution - Missense 15:51498788-51498788 - TCGA-IR-A3LK-01 COSM4755170 c.6031G>C p.D2011H Substitution - Missense 15:51481075-51481075 - 3206A7_017_T COSM5039284 c.979G>T p.V327F Substitution - Missense 15:51542459-51542459 - TCGA-B7-5816-01 COSM4055515 c.5804C>A p.P1935H Substitution - Missense 15:51481302-51481302 - TCGA-DA-A1IC-06 COSM3502097 c.1354C>T p.L452L Substitution - coding silent 15:51537751-51537751 - TCGA-EE-A3AE-06 COSM3502085 c.5141C>T p.S1714F Substitution - Missense 15:51488030-51488030 - TCGA-23-1124-01 COSM74386 c.2891T>C p.L964P Substitution - Missense 15:51502907-51502907 - TCGA-EE-A29L-06 COSM1708176 c.716C>T p.S239L Substitution - Missense 15:51547260-51547260 - TCGA-BR-8680-01 COSM4055519 c.4224A>C p.E1408D Substitution - Missense 15:51499000-51499000 - CSCC-60-T COSM4509480 c.8082C>T p.A2694A Substitution - coding silent 15:51458556-51458556 - HCC39T COSM1608470 c.4922A>C p.N1641T Substitution - Missense 15:51491609-51491609 - HCC2998 COSM2216975 c.6450A>C p.K2150N Substitution - Missense 15:51480656-51480656 - TCGA-DD-A1EL-01 COSM4925851 c.3832G>C p.V1278L Substitution - Missense 15:51499392-51499392 - T3080 COSM4678205 c.4807T>C p.W1603R Substitution - Missense 15:51491724-51491724 - TCGA-D9-A6EC-06 COSM4403469 c.3911A>C p.N1304T Substitution - Missense 15:51499313-51499313 - TCGA-BT-A2LB-01 COSM3794239 c.2960C>T p.S987L Substitution - Missense 15:51502838-51502838 - CRC-18T COSM5460623 c.1061C>T p.A354V Substitution - Missense 15:51542377-51542377 - TCGA-KV-A6GD-01 COSM3988002 c.2289A>C p.P763P Substitution - coding silent 15:51536191-51536191 - PT41 COSM555593 c.8971C>T p.R2991* Substitution - Nonsense 15:51449124-51449124 - CLL149 COSM1290398 c.402G>T p.L134F Substitution - Missense 15:51564223-51564223 - SNUH_G76_S1 COSM4419038 c.5946C>T p.H1982H Substitution - coding silent 15:51481160-51481160 - 587342 COSM1203893 c.2809C>A p.P937T Substitution - Missense 15:51502989-51502989 - 18T COSM106466 c.6834-5A>G p.? Unknown 15:51476721-51476721 - NCI-H226 COSM1678461 c.5420A>C p.D1807A Substitution - Missense 15:51486135-51486135 - TCGA-EB-A3Y7-01 COSM3502072 c.7905G>A p.K2635K Substitution - coding silent 15:51463397-51463397 - ESCC-018T COSM3936780 c.4143A>T p.I1381I Substitution - coding silent 15:51499081-51499081 - PR-00-1165 COSM244065 c.7272C>T p.L2424L Substitution - coding silent 15:51471340-51471340 - TCGA-22-5473-01 COSM701061 c.3376G>A p.D1126N Substitution - Missense 15:51499848-51499848 - WSU-HN13 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - ESO-161 COSM1250294 c.7381G>C p.V2461L Substitution - Missense 15:51471231-51471231 - TCGA-34-2600-01 COSM701053 c.698G>A p.R233Q Substitution - Missense 15:51547278-51547278 - HCT116 COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - TCGA-A6-5665-01 COSM1373430 c.2512G>A p.A838T Substitution - Missense 15:51517092-51517092 - TCGA-DD-A3A7-01 COSM4916216 c.591G>A p.W197* Substitution - Nonsense 15:51547385-51547385 - TCGA-24-2289-01 COSM117334 c.5946C>A p.H1982Q Substitution - Missense 15:51481160-51481160 - CPCG0413-F1 COSM4881132 c.6892C>T p.R2298C Substitution - Missense 15:51476658-51476658 - TCGA-H2-A2K9-01 COSM3370202 c.846G>T p.Q282H Substitution - Missense 15:51545667-51545667 - TCGA-HU-A4GH-01 COSM4055528 c.322T>G p.F108V Substitution - Missense 15:51565130-51565130 - ESCC-F93 COSM5049141 c.6094G>A p.D2032N Substitution - Missense 15:51481012-51481012 - cSCCP6 COSM137004 c.5558G>A p.R1853K Substitution - Missense 15:51481548-51481548 - CAL33 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - 199-06-01TD COSM4678204 c.5158C>T p.R1720C Substitution - Missense 15:51488013-51488013 - CSCC-27-T COSM4509007 c.7945C>T p.P2649S Substitution - Missense 15:51458774-51458774 - B106 COSM1749205 c.4676G>A p.R1559K Substitution - Missense 15:51495131-51495131 - 1 COSM4172184 c.7114_7125del12 p.A2372_P2375delAAHP Deletion - In frame 15:51474429-51474440 - TCGA-AC-A23H-01 COSM3816307 c.3874G>A p.E1292K Substitution - Missense 15:51499350-51499350 - MAVER-1 COSM1740176 c.8201C>A p.A2734E Substitution - Missense 15:51457398-51457398 - TCGA-CH-5738-01 COSM1129181 c.7432G>T p.D2478Y Substitution - Missense 15:51466269-51466269 - TCGA-13-2061-01 COSM1323951 c.2693A>T p.E898V Substitution - Missense 15:51507205-51507205 - BICR_22 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - UM-SCC-11B COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-AC-A5XS-01 COSM4391014 c.2242A>C p.I748L Substitution - Missense 15:51536238-51536238 - 108 COSM5016798 c.4777C>A p.H1593N Substitution - Missense 15:51495030-51495030 - ESO-887 COSM1250296 c.2713T>G p.S905A Substitution - Missense 15:51507185-51507185 - CSCC-27-T COSM4489502 c.3487C>T p.P1163S Substitution - Missense 15:51499737-51499737 - PT46 COSM5929564 c.7216C>T p.P2406S Substitution - Missense 15:51471396-51471396 - TCGA-D8-A1JA-01 COSM3816301 c.5955C>T p.A1985A Substitution - coding silent 15:51481151-51481151 - TCGA-AY-6197-01 COSM1373419 c.5161T>C p.F1721L Substitution - Missense 15:51488010-51488010 - GC8_T COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - LUAD-F00365 COSM340422 c.7285C>T p.P2429S Substitution - Missense 15:51471327-51471327 - BD6T COSM5499213 c.4931C>T p.T1644M Substitution - Missense 15:51491600-51491600 - CPCG0103-P8 COSM3396211 c.6008C>A p.A2003D Substitution - Missense 15:51481098-51481098 - TCGA-CG-4444-01 COSM4055509 c.8022T>C p.N2674N Substitution - coding silent 15:51458616-51458616 - TCGA-DR-A0ZM-01 COSM459007 c.6922G>C p.E2308Q Substitution - Missense 15:51476628-51476628 - CSCC-40-T COSM1203896 c.2486G>A p.R829Q Substitution - Missense 15:51517118-51517118 - SNUH_G16_S1 COSM147908 c.3862T>C p.S1288P Substitution - Missense 15:51499362-51499362 - YURUS COSM1708176 c.716C>T p.S239L Substitution - Missense 15:51547260-51547260 - 473 COSM4438100 c.6318G>C p.E2106D Substitution - Missense 15:51480788-51480788 - TCGA-D3-A3C8-06 COSM3502068 c.8963C>T p.S2988F Substitution - Missense 15:51449132-51449132 - 587222 COSM1203890 c.4085G>A p.R1362Q Substitution - Missense 15:51499139-51499139 - TCGA-EJ-5518-01 COSM1129182 c.8011-2A>G p.? Unknown 15:51458629-51458629 - PDA_074 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - SNUH_G76_S1 COSM1373437 c.1490C>T p.T497M Substitution - Missense 15:51537615-51537615 - PT52 COSM5940507 c.209G>A p.G70E Substitution - Missense 15:51576060-51576060 - TCGA-AA-A00N-01 COSM274809 c.6377G>A p.R2126H Substitution - Missense 15:51480729-51480729 - PTC-14C COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AP-A0L9-01 COSM962742 c.1234C>T p.R412* Substitution - Nonsense 15:51538324-51538324 - UM-SCC-47 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - HCC2998 COSM1678460 c.5655C>A p.F1885L Substitution - Missense 15:51481451-51481451 - B86 COSM1749204 c.6565G>A p.E2189K Substitution - Missense 15:51480139-51480139 - TCGA-09-2056-01 COSM70471 c.1703T>G p.I568R Substitution - Missense 15:51536777-51536777 - RKO COSM2217034 c.2631_2632insT p.Q878fs*21 Insertion - Frameshift 15:51514454-51514455 - CSCC-56-T COSM4461180 c.1195C>T p.H399Y Substitution - Missense 15:51538363-51538363 - CSCC-29-T COSM4545354 c.3769G>A p.D1257N Substitution - Missense 15:51499455-51499455 - TCGA-BR-8680-01 COSM4055511 c.7374T>G p.D2458E Substitution - Missense 15:51471238-51471238 - WA48 COSM239589 c.8341G>T p.G2781C Substitution - Missense 15:51456185-51456185 - PD24205a COSM5787270 c.3059C>G p.S1020C Substitution - Missense 15:51500165-51500165 - Au4 COSM5603380 c.3100A>G p.N1034D Substitution - Missense 15:51500124-51500124 - RKO COSM4647824 c.986T>C p.V329A Substitution - Missense 15:51542452-51542452 - LC_C6 COSM1189007 c.7696G>T p.G2566C Substitution - Missense 15:51464784-51464784 - TCGA-EE-A2MR-06 COSM3502092 c.3288T>A p.V1096V Substitution - coding silent 15:51499936-51499936 - PCA17-2 COSM5415751 c.2863A>G p.M955V Substitution - Missense 15:51502935-51502935 - UM-SCC-47 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-BS-A0UM-01 COSM962719 c.4721G>A p.R1574H Substitution - Missense 15:51495086-51495086 - TCGA-G2-A2EO-01 COSM1301216 c.6331G>C p.D2111H Substitution - Missense 15:51480775-51480775 - TCGA-D3-A51T-06 COSM3502086 c.4936C>A p.R1646R Substitution - coding silent 15:51491595-51491595 - Pat_24_A COSM5383482 c.7766G>A p.R2589Q Substitution - Missense 15:51464714-51464714 - BCM695T COSM4802862 c.3587G>A p.R1196K Substitution - Missense 15:51499637-51499637 - TCGA-AX-A0J0-01 COSM962703 c.7569G>T p.K2523N Substitution - Missense 15:51465600-51465600 - NOKSI COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-AP-A0LM-01 COSM962708 c.6710T>G p.I2237S Substitution - Missense 15:51479994-51479994 - TCGA-BK-A139-01 COSM962731 c.3188G>C p.S1063T Substitution - Missense 15:51500036-51500036 - TCGA-CA-6717-01 COSM1373421 c.4489A>C p.N1497H Substitution - Missense 15:51498735-51498735 - BD72T COSM5513088 c.2374C>T p.L792F Substitution - Missense 15:51535725-51535725 - SCC-9 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - DLD1 COSM1678462 c.4405T>C p.S1469P Substitution - Missense 15:51498819-51498819 - TCGA-AA-A010-01 COSM280448 c.265A>C p.N89H Substitution - Missense 15:51568507-51568507 - 169 COSM1373415 c.7474delT p.S2492fs*21 Deletion - Frameshift 15:51466227-51466227 - TCGA-HT-7689-01 COSM3969150 c.7156G>A p.G2386R Substitution - Missense 15:51474398-51474398 - LS174T COSM1373443 c.326delT p.L109fs*1 Deletion - Frameshift 15:51565126-51565126 - HCC122T COSM5808603 c.4295A>G p.Y1432C Substitution - Missense 15:51498929-51498929 - TCGA-DI-A0WH-01 COSM962716 c.5384C>A p.P1795H Substitution - Missense 15:51486171-51486171 - TCGA-HU-A4GP-01 COSM3816302 c.5534G>A p.R1845Q Substitution - Missense 15:51481572-51481572 - TCGA-ER-A19D-06 COSM3502080 c.6309C>T p.S2103S Substitution - coding silent 15:51480797-51480797 - TCGA-EE-A2GR-06 COSM3502070 c.8742C>T p.L2914L Substitution - coding silent 15:51450288-51450288 - TCGA-BR-8487-01 COSM4055530 c.108T>C p.D36D Substitution - coding silent 15:51576161-51576161 - LUAD-YINHD COSM349049 c.8146G>A p.D2716N Substitution - Missense 15:51457453-51457453 - 39 COSM3732718 c.4475A>C p.K1492T Substitution - Missense 15:51498749-51498749 - GHE0609 COSM5713464 c.2620_2621delGA p.E874fs*24 Deletion - Frameshift 15:51514465-51514466 - CAL27 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - RK223_C01 COSM4943666 c.364+3A>G p.? Unknown 15:51565085-51565085 - ESCC-D13 COSM5045368 c.2011C>T p.H671Y Substitution - Missense 15:51536469-51536469 - PTC-46C COSM4128288 c.89C>T p.A30V Substitution - Missense 15:51576180-51576180 - pfg316T COSM4755171 c.5336G>A p.C1779Y Substitution - Missense 15:51486219-51486219 - PT48 COSM5828247 c.88-3delT p.? Unknown 15:51576184-51576184 - TCGA-AX-A0J0-01 COSM962699 c.8802C>A p.L2934L Substitution - coding silent 15:51450228-51450228 - AOCS-133-1-9 COSM3981554 c.8784C>T p.D2928D Substitution - coding silent 15:51450246-51450246 - TCGA-B5-A0JY-01 COSM962706 c.7108C>T p.R2370W Substitution - Missense 15:51474446-51474446 - HCC39 COSM1608470 c.4922A>C p.N1641T Substitution - Missense 15:51491609-51491609 - RK057_C01 COSM3700973 c.6742A>G p.I2248V Substitution - Missense 15:51479962-51479962 - TCGA-BS-A0UV-01 COSM962732 c.3015T>G p.I1005M Substitution - Missense 15:51500209-51500209 - TCGA-BS-A0UF-01 COSM962698 c.8845G>A p.A2949T Substitution - Missense 15:51450185-51450185 - T2944 COSM555593 c.8971C>T p.R2991* Substitution - Nonsense 15:51449124-51449124 - BK0038 COSM4187166 c.8867A>G p.Y2956C Substitution - Missense 15:51450163-51450163 - PDA_083 COSM5002608 c.4015G>T p.V1339L Substitution - Missense 15:51499209-51499209 - PT48 COSM5933356 c.4953G>A p.K1651K Substitution - coding silent 15:51491578-51491578 - sysucc-311T COSM5478921 c.8103C>T p.I2701I Substitution - coding silent 15:51458535-51458535 - YUCHIME COSM1708172 c.7619C>T p.S2540L Substitution - Missense 15:51464861-51464861 - TCGA-ER-A19N-06 COSM3502071 c.8176C>T p.Q2726* Substitution - Nonsense 15:51457423-51457423 - TCGA-33-4583-01 COSM701057 c.1273G>T p.D425Y Substitution - Missense 15:51538285-51538285 - TCGA-AP-A0LM-01 COSM962718 c.4735C>A p.L1579I Substitution - Missense 15:51495072-51495072 - 587376 COSM1203895 c.6880C>A p.L2294I Substitution - Missense 15:51476670-51476670 - Pat_54_A COSM3502076 c.7276C>T p.P2426S Substitution - Missense 15:51471336-51471336 - TCGA-AP-A0LM-01 COSM962709 c.6639G>A p.A2213A Substitution - coding silent 15:51480065-51480065 - WSU-HN13 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AP-A056-01 COSM962724 c.4243G>T p.D1415Y Substitution - Missense 15:51498981-51498981 - UM-SCC-17B COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - WSU-HN8 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - AOCS-139-6-3 COSM3981557 c.4993G>A p.D1665N Substitution - Missense 15:51488606-51488606 - BRC16 COSM5027973 c.6430C>T p.R2144* Substitution - Nonsense 15:51480676-51480676 - TCGA-GF-A6C9-06 COSM4900411 c.1007C>T p.P336L Substitution - Missense 15:51542431-51542431 - WSU-HN6 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - 24T COSM107064 c.4473C>A p.N1491K Substitution - Missense 15:51498751-51498751 - 93VU147T COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - TCGA-F1-6875-01 COSM4055508 c.8225C>G p.S2742C Substitution - Missense 15:51457374-51457374 - YUPROST COSM1708171 c.8789_8790GG>CT p.R2930T Substitution - Missense 15:51450240-51450241 - CDGLIV0707A0251_T COSM5040469 c.5540A>T p.H1847L Substitution - Missense 15:51481566-51481566 - QC2-22-T2 COSM5249724 c.3697_3699delCTT p.L1233delL Deletion - In frame 15:51499525-51499527 - TCGA-EI-6917-01 COSM3420408 c.4937G>A p.R1646Q Substitution - Missense 15:51491594-51491594 - HCC20T COSM1608471 c.4367A>G p.Y1456C Substitution - Missense 15:51498857-51498857 - ESCC_107 COSM5638450 c.3832G>A p.V1278I Substitution - Missense 15:51499392-51499392 - WSU-HN30 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - CSCC-27-T COSM4495555 c.4567C>T p.L1523L Substitution - coding silent 15:51498657-51498657 - TCGA-AA-3510-01 COSM1373441 c.1213G>A p.E405K Substitution - Missense 15:51538345-51538345 - TCGA-EE-A3AA-06 COSM3502082 c.5778C>T p.F1926F Substitution - coding silent 15:51481328-51481328 - TCGA-AK-3430-01 COSM470794 c.566A>G p.K189R Substitution - Missense 15:51563382-51563382 - T3080 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - HCC2998 COSM1678460 c.5655C>A p.F1885L Substitution - Missense 15:51481451-51481451 - TCGA-CA-6717-01 COSM1373433 c.1768C>T p.H590Y Substitution - Missense 15:51536712-51536712 - YUPAER COSM5383483 c.6293C>T p.S2098F Substitution - Missense 15:51480813-51480813 - SJHGG056_A COSM4971062 c.8539-4G>A p.? Unknown 15:51453645-51453645 - BD120T COSM5514682 c.1744G>C p.E582Q Substitution - Missense 15:51536736-51536736 - PTC-28C COSM4128291 c.27A>G p.G9G Substitution - coding silent 15:51622519-51622519 - HCC03T COSM131172 c.5351C>T p.S1784L Substitution - Missense 15:51486204-51486204 - TCGA-G4-6588-01 COSM1373423 c.3794A>G p.D1265G Substitution - Missense 15:51499430-51499430 - 8067242 COSM2217070 c.758G>A p.C253Y Substitution - Missense 15:51545755-51545755 - YUPAER COSM5383484 c.5944C>T p.H1982Y Substitution - Missense 15:51481162-51481162 - TCGA-D1-A17H-01 COSM962737 c.2185C>T p.R729C Substitution - Missense 15:51536295-51536295 - 8015299 COSM1243211 c.2651G>A p.R884H Substitution - Missense 15:51507247-51507247 - TCGA-DD-A4NS-01 COSM4926382 c.172A>G p.I58V Substitution - Missense 15:51576097-51576097 - TCGA-A6-5665-01 COSM1373426 c.2972T>C p.I991T Substitution - Missense 15:51502826-51502826 - TCGA-B0-5709-01 COSM470790 c.5292T>C p.T1764T Substitution - coding silent 15:51486263-51486263 - T3225 COSM1373420 c.5084delT p.F1695fs*15 Deletion - Frameshift 15:51488087-51488087 - TCGA-JW-A5VJ-01 COSM4818615 c.167G>C p.G56A Substitution - Missense 15:51576102-51576102 - HCC126T COSM3706619 c.4748T>A p.L1583Q Substitution - Missense 15:51495059-51495059 - TCGA-DR-A0ZM-01 COSM459006 c.781C>A p.H261N Substitution - Missense 15:51545732-51545732 - TCGA-EI-6917-01 COSM2217021 c.3567G>A p.A1189A Substitution - coding silent 15:51499657-51499657 - HCC028T COSM5807741 c.3197G>A p.S1066N Substitution - Missense 15:51500027-51500027 - TCGA-AC-A23H-01 COSM3816300 c.6256G>A p.E2086K Substitution - Missense 15:51480850-51480850 - TCGA-EB-A24D-01 COSM3502093 c.3160A>C p.M1054L Substitution - Missense 15:51500064-51500064 - AOCS-097-1-X COSM3981555 c.6719T>G p.M2240R Substitution - Missense 15:51479985-51479985 - UM-SCC-11B COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-BS-A0UF-01 COSM962710 c.6407C>T p.A2136V Substitution - Missense 15:51480699-51480699 - TCGA-FS-A4FB-06 COSM3502076 c.7276C>T p.P2426S Substitution - Missense 15:51471336-51471336 - TCGA-CA-6717-01 COSM280448 c.265A>C p.N89H Substitution - Missense 15:51568507-51568507 - 75 COSM3732775 c.5976T>A p.D1992E Substitution - Missense 15:51481130-51481130 - TCGA-BR-8680-01 COSM4055510 c.7910G>T p.R2637I Substitution - Missense 15:51463392-51463392 - TCGA-EE-A29H-06 COSM3502074 c.7575C>T p.F2525F Substitution - coding silent 15:51465594-51465594 - TCGA-A8-A097-01 COSM434018 c.4844A>G p.N1615S Substitution - Missense 15:51491687-51491687 - TCGA-BG-A0M4-01 COSM962741 c.1730C>T p.T577M Substitution - Missense 15:51536750-51536750 - TCGA-33-4583-01 COSM701055 c.1272T>G p.D424E Substitution - Missense 15:51538286-51538286 - QC2-25-T2 COSM5653348 c.6046G>C p.D2016H Substitution - Missense 15:51481060-51481060 - TCGA-BT-A20R-01 COSM1301212 c.7396C>G p.L2466V Substitution - Missense 15:51466305-51466305 - TCGA-ET-A2MY-01 COSM3370201 c.3548T>C p.L1183P Substitution - Missense 15:51499676-51499676 - WSU-HN30 COSM4128282 c.7114G>T p.A2372S Substitution - Missense 15:51474440-51474440 - STC291 COSM5054338 c.5973C>T p.D1991D Substitution - coding silent 15:51481133-51481133 - TCGA-EI-6884-01 COSM3420405 c.9019C>A p.R3007R Substitution - coding silent 15:51449076-51449076 - YUKLAB COSM1708173 c.5210C>T p.A1737V Substitution - Missense 15:51487961-51487961 - PDA_052 COSM5000776 c.5978C>T p.A1993V Substitution - Missense 15:51481128-51481128 - TCGA-B5-A11E-01 COSM962736 c.2240G>A p.R747Q Substitution - Missense 15:51536240-51536240 - TCGA-GN-A26C-01 COSM3502081 c.6151C>T p.L2051F Substitution - Missense 15:51480955-51480955 - TCGA-E2-A1IH-01 COSM1478183 c.8756G>A p.G2919D Substitution - Missense 15:51450274-51450274 - 587350 COSM1203891 c.2617A>C p.T873P Substitution - Missense 15:51514469-51514469 - BCM695T COSM4802862 c.3587G>A p.R1196K Substitution - Missense 15:51499637-51499637 - EOPC-030_tumor COSM4640005 c.7958C>T p.A2653V Substitution - Missense 15:51458761-51458761 - HCC17T COSM1608468 c.8972G>A p.R2991Q Substitution - Missense 15:51449123-51449123 - TCGA-C4-A0EZ-01 COSM416903 c.4670C>T p.S1557L Substitution - Missense 15:51498554-51498554 - S00050 COSM317240 c.3421G>C p.V1141L Substitution - Missense 15:51499803-51499803 - TCGA-BR-8361-01 COSM4055529 c.214-2A>T p.? Unknown 15:51568560-51568560 - CSCC-49-T COSM4572547 c.7802T>G p.F2601C Substitution - Missense 15:51464678-51464678 - T578 COSM4678202 c.7599C>A p.F2533L Substitution - Missense 15:51465570-51465570 - TCGA-B5-A0JY-01 COSM962702 c.8456A>G p.N2819S Substitution - Missense 15:51456070-51456070 - TCGA-EE-A2MR-06 COSM3502088 c.4411C>T p.L1471L Substitution - coding silent 15:51498813-51498813 - TCGA-G4-6293-01 COSM1373424 c.3488C>T p.P1163L Substitution - Missense 15:51499736-51499736 - pfg065T COSM4747235 c.2625_2626delAT p.F877fs*21 Deletion - Frameshift 15:51514460-51514461 - 61 COSM5740343 c.7319C>T p.A2440V Substitution - Missense 15:51471293-51471293 - 1N26-VS-1T26 COSM4973483 c.1487A>G p.E496G Substitution - Missense 15:51537618-51537618 - HCT8 COSM4633987 c.4635T>C p.S1545S Substitution - coding silent 15:51498589-51498589 - TCGA-GD-A3OP-01 COSM1301213 c.6537C>G p.L2179L Substitution - coding silent 15:51480569-51480569 - 2290930 COSM4440391 c.6649delA p.T2217fs*3 Deletion - Frameshift 15:51480055-51480055 - ESCC_168 COSM5648716 c.33C>G p.V11V Substitution - coding silent 15:51622513-51622513 - I2L-P19Ta-Tumor-Biopsy COSM5362912 c.4255G>T p.D1419Y Substitution - Missense 15:51498969-51498969 - LUAD-S01306 COSM343478 c.5384C>T p.P1795L Substitution - Missense 15:51486171-51486171 - TCGA-AA-3662-01 COSM1373422 c.4114G>T p.V1372L Substitution - Missense 15:51499110-51499110 - BHY COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AP-A0LP-01 COSM962730 c.3232T>C p.Y1078H Substitution - Missense 15:51499992-51499992 - TCGA-EE-A2GH-06 COSM3502090 c.4057T>C p.L1353L Substitution - coding silent 15:51499167-51499167 - PTC-515C COSM4128291 c.27A>G p.G9G Substitution - coding silent 15:51622519-51622519 - CSCC-5-T COSM4555969 c.6745G>A p.E2249K Substitution - Missense 15:51479959-51479959 - TCGA-A3-3370-01 COSM470792 c.770T>G p.L257* Substitution - Nonsense 15:51545743-51545743 - TCGA-AA-A010-01 COSM280447 c.725A>C p.K242T Substitution - Missense 15:51547251-51547251 - TCGA-GF-A6C9-06 COSM4900670 c.2786C>T p.S929F Substitution - Missense 15:51503012-51503012 - WSU-HN12 COSM1740185 c.7115C>T p.A2372V Substitution - Missense 15:51474439-51474439 - TCGA-AA-3833-01 COSM271211 c.718T>C p.W240R Substitution - Missense 15:51547258-51547258 - 2492729 COSM5729705 c.7579C>T p.P2527S Substitution - Missense 15:51465590-51465590 - TCGA-EE-A17Y-06 COSM3502099 c.1323T>C p.G441G Substitution - coding silent 15:51538235-51538235 - TCGA-AP-A051-01 COSM962726 c.3774G>A p.G1258G Substitution - coding silent 15:51499450-51499450 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.511367;Hs.511386 15q21.2 612186

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - InFrameDeletion p.L1233delL c.3697_3699delCTT 15 51791722 LGG A C IntronicSNV . c.285+148T>G 15 51860536 DLBCL A C Missense p.D424E c.1272T>G 15 51830483 LUSC A C Missense p.I568R c.1703T>G 15 51828974 OV A C Missense p.S905A c.2713T>G 15 51799382 ESCA A C Missense p.Y2572D c.7714T>G 15 51756966 LUAD A C Nonsense p.L257* c.770T>G 15 51837940 RCCC A G IntronicSNV . c.88-3771T>C 15 51872149 CLL A G Missense p.F782S c.2345T>C 15 51827951 OV A G Missense p.L1183P c.3548T>C 15 51791873 THCA A G Missense p.L2977P c.8930T>C 15 51741365 RCCC A G Missense p.L964P c.2891T>C 15 51795104 OV A G Missense p.V2624A c.7871T>C 15 51755631 LUSC A G Missense p.V2788A c.8363T>C 15 51748363 STAD A G Missense p.Y1078H c.3232T>C 15 51792189 UCEC A G Synonymous p.F1893F c.5679T>C 15 51773624 CM A G Synonymous p.G441G c.1323T>C 15 51830432 CM A G Synonymous p.I2212I c.6636T>C 15 51772265 HNSC A G Synonymous p.L1353L c.4057T>C 15 51791364 CM A G Synonymous p.N2675N c.8025T>C 15 51750813 STAD A G Synonymous p.P2407P c.7221T>C 15 51763591 UCEC A G Synonymous p.S2857S c.8571T>C 15 51745809 HC A G Synonymous p.T1764T c.5292T>C 15 51778460 RCCC A - IntronicDeletion . c.7214-19delT 15 51763617 STAD A T Missense p.L1537M c.4609T>A 15 51790812 STAD A T Missense p.N1190K c.3570T>A 15 51791851 OV A T Nonsense p.C1105* c.3315T>A 15 51792106 ESCA C A IntronicSNV . c.7214-1464G>T 15 51765062 CLL C A Missense p.D2032Y c.6094G>T 15 51773209 RCCC C A Missense p.D2563Y c.7687G>T 15 51756993 COREAD C A Missense p.D425Y c.1273G>T 15 51830482 LUSC C A Missense p.G938V c.2813G>T 15 51795182 CM C A Missense p.L134F c.402G>T 15 51856420 CLL C A Missense p.M247I c.741G>T 15 51839432 LUSC C A Missense p.Q282H c.846G>T 15 51837864 THCA C A Missense p.V1541L c.4621G>T 15 51790800 RCCC C A Missense p.V1740L c.5218G>T 15 51778534 BRCA C A Missense p.V63L c.187G>T 15 51868279 UCEC C A Missense p.W268L c.803G>T 15 51837907 STAD C A Nonsense p.E439* c.1315G>T 15 51830440 CM C A SpliceAcceptorSNV . c.1106-1G>T 15 51830650 BRCA C A Synonymous p.L452L c.1356G>T 15 51829946 LUAD C A Synonymous p.T577T c.1731G>T 15 51828946 LUSC C G Missense p.D1977H c.5929G>C 15 51773374 BLCA C G Missense p.D2111H c.6331G>C 15 51772972 BLCA C G Missense p.E455Q c.1363G>C 15 51829939 BRCA C G Missense p.E471Q c.1411G>C 15 51829891 BRCA C G Missense p.E582D c.1746G>C 15 51828931 OV C G Missense p.E874Q c.2620G>C 15 51806663 HNSC C G Missense p.G1258R c.3772G>C 15 51791649 RCCC C G Missense p.L1709F c.5127G>C 15 51780241 BRCA C G Missense p.R1234T c.3701G>C 15 51791720 BLCA C G Missense p.R2132T c.6395G>C 15 51772908 BLCA C G Missense p.R747P c.2240G>C 15 51828437 BRCA C G Missense p.S1063T c.3188G>C 15 51792233 UCEC C G Missense p.V1141L c.3421G>C 15 51792000 SCLC C G Missense p.V1541L c.4621G>C 15 51790800 STAD C G Missense p.V2462L c.7384G>C 15 51763428 ESCA C G Missense p.V538L c.1612G>C 15 51829690 STAD C G Missense p.W197C c.591G>C 15 51839582 RCCC C G SpliceAcceptorSNV . c.8634-1G>C 15 51743895 LUAD C G Synonymous p.V2323V c.6969G>C 15 51766785 BRCA C T IntronicSNV . c.8274+37G>A 15 51749488 CM C T Missense p.A924T c.2770G>A 15 51795225 CLL C T Missense p.D1126N c.3376G>A 15 51792045 LUSC C T Missense p.D1813N c.5437G>A 15 51778315 COREAD C T Missense p.D2494N c.7480G>A 15 51758421 CM C T Missense p.E2114K c.6340G>A 15 51772963 BLCA C T Missense p.E2480K c.7438G>A 15 51758463 BLCA C T Missense p.E926K c.2776G>A 15 51795219 CM C T Missense p.G1225R c.3673G>A 15 51791748 CM C T Missense p.G2387R c.7159G>A 15 51766595 LGG C T Missense p.G2920D c.8759G>A 15 51742471 BRCA C T Missense p.G387D c.1160G>A 15 51830595 CM C T Missense p.M2177I c.6531G>A 15 51772772 CM C T Missense p.R1025H c.3074G>A 15 51792347 LUAD C T Missense p.R1234K c.3701G>A 15 51791720 BLCA C T Missense p.R1397Q c.4190G>A 15 51791231 CM C T Missense p.R1574H c.4721G>A 15 51787283 MM C T Missense p.R1574H c.4721G>A 15 51787283 UCEC C T Missense p.R1705Q c.5114G>A 15 51780254 STAD C T Missense p.R2144Q c.6431G>A 15 51772872 COREAD C T Missense p.R233Q c.698G>A 15 51839475 LUSC C T Missense p.R2719H c.8156G>A 15 51749643 BRCA C T Missense p.S1063N c.3188G>A 15 51792233 COREAD C T Missense p.V419I c.1255G>A 15 51830500 CM C T Nonsense p.W118* c.353G>A 15 51857296 CM C T Nonsense p.W177* c.531G>A 15 51855614 PRAD C T Nonsense p.W203* c.609G>A 15 51839564 COREAD C T Nonsense p.W910* c.2730G>A 15 51799365 HNSC C T SpliceDonorSNV . c.2992+1G>A 15 51795002 PRAD G A IntronicSNV . c.7927-84C>T 15 51751076 CM G A IntronicSNV . c.8014-25C>T 15 51750849 CM G A Missense p.A1916V c.5747C>T 15 51773556 CM G A Missense p.A2360V c.7079C>T 15 51766675 CM G A Missense p.H1517Y c.4549C>T 15 51790872 HNSC G A Missense p.H2521Y c.7561C>T 15 51757808 HNSC G A Missense p.H433Y c.1297C>T 15 51830458 NSCLC G A Missense p.H716Y c.2146C>T 15 51828531 CM G A Missense p.L1125F c.3373C>T 15 51792048 CM G A Missense p.L1844F c.5530C>T 15 51773773 CM G A Missense p.L2051F c.6151C>T 15 51773152 CM G A Missense p.P1427S c.4279C>T 15 51791142 CM G A Missense p.S1557L c.4670C>T 15 51790751 BLCA G A Missense p.S1714F c.5141C>T 15 51780227 CM G A Missense p.S2123F c.6368C>T 15 51772935 CM G A Missense p.S239L c.716C>T 15 51839457 CM G A Missense p.S2404L c.7211C>T 15 51766543 CM G A Missense p.S2607F c.7820C>T 15 51755682 LUAD G A Missense p.S2918L c.8753C>T 15 51742477 CM G A Missense p.S2989F c.8966C>T 15 51741329 CM G A Missense p.S451F c.1352C>T 15 51829950 CM G A Missense p.S987L c.2960C>T 15 51795035 BLCA G A Nonsense p.Q2727* c.8179C>T 15 51749620 CM G A Nonsense p.Q539* c.1615C>T 15 51829687 BRCA G A Nonsense p.Q96* c.286C>T 15 51857363 CM G A Nonsense p.R2144* c.6430C>T 15 51772873 BRCA G A Nonsense p.R2992* c.8974C>T 15 51741321 HNSC G A Nonsense p.R2992* c.8974C>T 15 51741321 LUAD G A Synonymous p.C1897C c.5691C>T 15 51773612 CM G A Synonymous p.C99C c.297C>T 15 51857352 STAD G A Synonymous p.D856D c.2568C>T 15 51806715 CM G A Synonymous p.F1533F c.4599C>T 15 51790822 CM G A Synonymous p.F1926F c.5778C>T 15 51773525 CM G A Synonymous p.F2526F c.7578C>T 15 51757791 CM G A Synonymous p.G34G c.102C>T 15 51868364 CM G A Synonymous p.H2416H c.7248C>T 15 51763564 CM G A Synonymous p.L2977L c.8929C>T 15 51741366 CM G A Synonymous p.L452L c.1354C>T 15 51829948 CM G A Synonymous p.S2103S c.6309C>T 15 51772994 CM GC AT Missense p.S823N c.2468_2469delinsAT 15 51809332 HNSC G C IntronicSNV . c.214-50C>G 15 51860805 NSCLC G C IntronicSNV . c.7927-1751C>G 15 51752743 HC G C Missense p.F1026L c.3078C>G 15 51792343 BLCA G C Missense p.L2234V c.6700C>G 15 51772201 STAD G C Missense p.L2467V c.7399C>G 15 51758502 BLCA G C Missense p.Q1818E c.5452C>G 15 51778300 HNSC G C Synonymous p.L2179L c.6537C>G 15 51772766 BLCA G T Missense p.A1602D c.4805C>A 15 51783923 STAD G T Missense p.H1982Q c.5946C>A 15 51773357 OV G T Missense p.L1340I c.4018C>A 15 51791403 BRCA G T Missense p.L2051I c.6151C>A 15 51773152 HNSC G T Missense p.N3031K c.9093C>A 15 51741202 BLCA G T Missense p.Q2194K c.6580C>A 15 51772321 CLL G T Nonsense p.S1765* c.5294C>A 15 51778458 RCCC T A Missense p.H2985L c.8954A>T 15 51741341 LUAD T A Missense p.Q2697L c.8090A>T 15 51750748 LUSC T A Synonymous p.S259S c.777A>T 15 51837933 CM T C IntronicSNV . c.285+561A>G 15 51860123 HC T C Missense p.D1875G c.5624A>G 15 51773679 LGG T C Missense p.K1674R c.5021A>G 15 51780775 LUAD T C Missense p.K1913E c.5737A>G 15 51773566 BLCA T C Missense p.K560E c.1678A>G 15 51828999 LUSC T C Missense p.N1615S c.4844A>G 15 51783884 BRCA T C Missense p.Q2496R c.7487A>G 15 51758414 RCCC T C Missense p.Y1501C c.4502A>G 15 51790919 CM T C SpliceAcceptorSNV . c.8014-2A>G 15 51750826 PRAD T C Synonymous p.G188G c.564A>G 15 51855581 BRCA T C Synonymous p.K2008K c.6024A>G 15 51773279 BRCA T - Frameshift p.T2022Hfs*16 c.6064delA 15 51773239 CM T G Missense p.M1054L c.3160A>C 15 51792261 CM T G Synonymous p.P485P c.1455A>C 15 51829847 OV