Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 15 50757299 50757299 + Missense_Mutation SNP G G C TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr15:50757299G>C c.597G>C c.(595-597)ttG>ttC p.L199F BLCA 15 50757369 50757369 + Missense_Mutation SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr15:50757369G>A c.667G>A c.(667-669)Gaa>Aaa p.E223K BLCA 15 50763921 50763921 + Missense_Mutation SNP G G C TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr15:50763921G>C c.778G>C c.(778-780)Gac>Cac p.D260H BLCA 15 50769147 50769147 + Silent SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr15:50769147C>T c.951C>T c.(949-951)gtC>gtT p.V317V BLCA 15 50769184 50769184 + Missense_Mutation SNP A A G TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr15:50769184A>G c.988A>G c.(988-990)Atc>Gtc p.I330V BLCA 15 50769684 50769684 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr15:50769684G>A c.1206G>A c.(1204-1206)aaG>aaA p.K402K BLCA 15 50773678 50773678 + Splice_Site SNP A A T TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr15:50773678A>T c.1219A>T c.(1219-1221)Att>Ttt p.I407F BLCA 15 50773824 50773824 + Silent SNP C C T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr15:50773824C>T c.1365C>T c.(1363-1365)ctC>ctT p.L455L BLCA 15 50773861 50773861 + Missense_Mutation SNP G G A TCGA-XF-AAMY-01A-11D-A42E-08 TCGA-XF-AAMY-10A-01D-A42H-08 g.chr15:50773861G>A c.1402G>A c.(1402-1404)Gaa>Aaa p.E468K BLCA 15 50774154 50774154 + Missense_Mutation SNP G G C TCGA-YC-A9TC-01A-22D-A391-08 TCGA-YC-A9TC-10A-01D-A394-08 g.chr15:50774154G>C c.1695G>C c.(1693-1695)aaG>aaC p.K565N BLCA 15 50776508 50776508 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:50776508C>A c.1840C>A c.(1840-1842)Cta>Ata p.L614I BLCA 15 50776527 50776527 + Missense_Mutation SNP G G A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr15:50776527G>A c.1859G>A c.(1858-1860)aGa>aAa p.R620K BLCA 15 50782478 50782478 + Missense_Mutation SNP G G A TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr15:50782478G>A c.1990G>A c.(1990-1992)Gga>Aga p.G664R BLCA 15 50782585 50782585 + Missense_Mutation SNP G G C TCGA-FD-A3NA-01A-11D-A21A-08 TCGA-FD-A3NA-10A-01D-A21A-08 g.chr15:50782585G>C c.2097G>C c.(2095-2097)aaG>aaC p.K699N BLCA 15 50782647 50782647 + Missense_Mutation SNP C C A TCGA-BT-A0S7-01A-11D-A10S-08 TCGA-BT-A0S7-10A-01D-A10S-08 g.chr15:50782647C>A c.2159C>A c.(2158-2160)cCa>cAa p.P720Q BLCA 15 50784944 50784944 + Missense_Mutation SNP C C G TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr15:50784944C>G c.2281C>G c.(2281-2283)Cag>Gag p.Q761E BLCA 15 50785037 50785037 + Silent SNP T T C TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr15:50785037T>C c.2374T>C c.(2374-2376)Ttg>Ctg p.L792L BLCA 15 50789403 50789403 + Missense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr15:50789403C>T c.3013C>T c.(3013-3015)Cct>Tct p.P1005S BLCA 15 50790854 50790854 + Missense_Mutation SNP A A T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:50790854A>T c.3100A>T c.(3100-3102)Aat>Tat p.N1034Y BRCA 15 50741617 50741617 + Silent SNP T T G TCGA-E2-A1LK-01A-21D-A14G-09 TCGA-E2-A1LK-11A-12D-A14G-09 g.chr15:50741617T>G c.270T>G c.(268-270)ctT>ctG p.L90L BRCA 15 50751285 50751285 + Missense_Mutation SNP G G A TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr15:50751285G>A c.424G>A c.(424-426)Gga>Aga p.G142R BRCA 15 50769138 50769138 + Silent SNP T T C TCGA-A2-A1G4-01A-11D-A13L-09 TCGA-A2-A1G4-10A-01W-A14R-09 g.chr15:50769138T>C c.942T>C c.(940-942)aaT>aaC p.N314N BRCA 15 50773883 50773883 + Missense_Mutation SNP A A C TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:50773883A>C c.1424A>C c.(1423-1425)aAa>aCa p.K475T BRCA 15 50773900 50773900 + Nonsense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:50773900G>T c.1441G>T c.(1441-1443)Gaa>Taa p.E481* BRCA 15 50782481 50782481 + Missense_Mutation SNP A A C TCGA-A7-A3J1-01A-11D-A20S-09 TCGA-A7-A3J1-10A-01D-A20S-09 g.chr15:50782481A>C c.1993A>C c.(1993-1995)Acc>Ccc p.T665P BRCA 15 50782646 50782646 + Missense_Mutation SNP C C G TCGA-E2-A10B-01A-11D-A10M-09 TCGA-E2-A10B-10A-01D-A10M-09 g.chr15:50782646C>G c.2158C>G c.(2158-2160)Cca>Gca p.P720A BRCA 15 50784950 50784950 + Missense_Mutation SNP C C T TCGA-OL-A66K-01A-11D-A29N-09 TCGA-OL-A66K-10A-01D-A29N-09 g.chr15:50784950C>T c.2287C>T c.(2287-2289)Cgg>Tgg p.R763W BRCA 15 50784955 50784955 + Missense_Mutation SNP C C A TCGA-OL-A66K-01A-11D-A29N-09 TCGA-OL-A66K-10A-01D-A29N-09 g.chr15:50784955C>A c.2292C>A c.(2290-2292)aaC>aaA p.N764K BRCA 15 50786430 50786430 + Missense_Mutation SNP G G C TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr15:50786430G>C c.2611G>C c.(2611-2613)Gaa>Caa p.E871Q CESC 15 50741664 50741664 + Missense_Mutation SNP C C G TCGA-HM-A4S6-01A-11D-A26G-09 TCGA-HM-A4S6-10A-01D-A26G-09 g.chr15:50741664C>G c.317C>G c.(316-318)tCt>tGt p.S106C CESC 15 50751336 50751336 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr15:50751336G>C c.475G>C c.(475-477)Gat>Cat p.D159H CESC 15 50776513 50776513 + Silent SNP G G A TCGA-IR-A3LI-01A-11D-A20U-09 TCGA-IR-A3LI-10A-01D-A20U-09 g.chr15:50776513G>A c.1845G>A c.(1843-1845)agG>agA p.R615R CESC 15 50782647 50782647 + Missense_Mutation SNP C C A TCGA-C5-A1BI-01B-11D-A13W-08 TCGA-C5-A1BI-10A-01D-A13W-08 g.chr15:50782647C>A c.2159C>A c.(2158-2160)cCa>cAa p.P720Q CESC 15 50785054 50785054 + Silent SNP C C T TCGA-DG-A2KH-01A-21D-A22X-09 TCGA-DG-A2KH-10A-01D-A22X-09 g.chr15:50785054C>T c.2391C>T c.(2389-2391)aaC>aaT p.N797N CESC 15 50786321 50786321 + Missense_Mutation SNP G G T TCGA-EK-A3GJ-01A-21D-A20U-09 TCGA-EK-A3GJ-11A-11D-A20U-09 g.chr15:50786321G>T c.2502G>T c.(2500-2502)atG>atT p.M834I CESC 15 50788052 50788052 + Missense_Mutation SNP A A C TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr15:50788052A>C c.2666A>C c.(2665-2667)aAt>aCt p.N889T CHOL 15 50785016 50785016 + Missense_Mutation SNP A A G TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr15:50785016A>G c.2353A>G c.(2353-2355)Act>Gct p.T785A CHOL 15 50785054 50785054 + Silent SNP C C T TCGA-W5-AA2H-01A-31D-A417-09 TCGA-W5-AA2H-10A-01D-A41A-09 g.chr15:50785054C>T c.2391C>T c.(2389-2391)aaC>aaT p.N797N CHOL 15 50785054 50785054 + Silent SNP C C T TCGA-W5-AA2T-01A-12D-A417-09 TCGA-W5-AA2T-10A-01D-A41A-09 g.chr15:50785054C>T c.2391C>T c.(2389-2391)aaC>aaT p.N797N CHOL 15 50785054 50785054 + Silent SNP C C T TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr15:50785054C>T c.2391C>T c.(2389-2391)aaC>aaT p.N797N COAD 15 50731368 50731368 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:50731368C>A c.98C>A c.(97-99)aCt>aAt p.T33N COAD 15 50733601 50733601 + Missense_Mutation SNP C C T TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr15:50733601C>T c.160C>T c.(160-162)Cgt>Tgt p.R54C COAD 15 50733660 50733661 + Frame_Shift_Ins INS - - A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:50733660_50733661insA c.219_220insA c.(220-222)aaafs p.K74fs COAD 15 50733676 50733676 + Missense_Mutation SNP T T C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:50733676T>C c.235T>C c.(235-237)Ttc>Ctc p.F79L COAD 15 50733676 50733676 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr15:50733676T>C c.235T>C c.(235-237)Ttc>Ctc p.F79L COAD 15 50733678 50733678 + Missense_Mutation SNP C C A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr15:50733678C>A c.237C>A c.(235-237)ttC>ttA p.F79L COAD 15 50751267 50751268 + Frame_Shift_Ins INS - - A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:50751267_50751268insA c.406_407insA c.(406-408)caafs p.Q136fs COAD 15 50763915 50763915 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:50763915C>T c.772C>T c.(772-774)Ctt>Ttt p.L258F COAD 15 50769174 50769174 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:50769174A>C c.978A>C c.(976-978)gaA>gaC p.E326D COAD 15 50773954 50773954 + Nonsense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr15:50773954C>T c.1495C>T c.(1495-1497)Caa>Taa p.Q499* COAD 15 50782025 50782025 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:50782025C>T c.1918C>T c.(1918-1920)Cga>Tga p.R640* COAD 15 50782562 50782562 + Missense_Mutation SNP A A G TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr15:50782562A>G c.2074A>G c.(2074-2076)Acc>Gcc p.T692A COAD 15 50788249 50788249 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:50788249C>T c.2863C>T c.(2863-2865)Cca>Tca p.P955S COAD 15 50789322 50789322 + Missense_Mutation SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:50789322A>C c.2932A>C c.(2932-2934)Aca>Cca p.T978P COADREAD 15 50731368 50731368 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:50731368C>A c.98C>A c.(97-99)aCt>aAt p.T33N COADREAD 15 50733601 50733601 + Missense_Mutation SNP C C T TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr15:50733601C>T c.160C>T c.(160-162)Cgt>Tgt p.R54C COADREAD 15 50733660 50733661 + Frame_Shift_Ins INS - - A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:50733660_50733661insA c.219_220insA c.(220-222)aaafs p.K74fs COADREAD 15 50733676 50733676 + Missense_Mutation SNP T T C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:50733676T>C c.235T>C c.(235-237)Ttc>Ctc p.F79L COADREAD 15 50733676 50733676 + Missense_Mutation SNP T T C TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr15:50733676T>C c.235T>C c.(235-237)Ttc>Ctc p.F79L COADREAD 15 50733678 50733678 + Missense_Mutation SNP C C A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr15:50733678C>A c.237C>A c.(235-237)ttC>ttA p.F79L COADREAD 15 50751267 50751268 + Frame_Shift_Ins INS - - A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:50751267_50751268insA c.406_407insA c.(406-408)caafs p.Q136fs COADREAD 15 50763915 50763915 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:50763915C>T c.772C>T c.(772-774)Ctt>Ttt p.L258F COADREAD 15 50769174 50769174 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:50769174A>C c.978A>C c.(976-978)gaA>gaC p.E326D COADREAD 15 50773953 50773953 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:50773953A>G c.1494A>G c.(1492-1494)gaA>gaG p.E498E COADREAD 15 50773954 50773954 + Nonsense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr15:50773954C>T c.1495C>T c.(1495-1497)Caa>Taa p.Q499* COADREAD 15 50782025 50782025 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:50782025C>T c.1918C>T c.(1918-1920)Cga>Tga p.R640* COADREAD 15 50782562 50782562 + Missense_Mutation SNP A A G TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr15:50782562A>G c.2074A>G c.(2074-2076)Acc>Gcc p.T692A COADREAD 15 50782647 50782647 + Missense_Mutation SNP C C A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr15:50782647C>A c.2159C>A c.(2158-2160)cCa>cAa p.P720Q COADREAD 15 50784958 50784958 + Silent SNP C C A TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr15:50784958C>A c.2295C>A c.(2293-2295)ctC>ctA p.L765L COADREAD 15 50786372 50786372 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:50786372A>C c.2553A>C c.(2551-2553)aaA>aaC p.K851N COADREAD 15 50788249 50788249 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr15:50788249C>T c.2863C>T c.(2863-2865)Cca>Tca p.P955S COADREAD 15 50789322 50789322 + Missense_Mutation SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:50789322A>C c.2932A>C c.(2932-2934)Aca>Cca p.T978P ESCA 15 50733646 50733646 + Missense_Mutation SNP G G T TCGA-JY-A6F8-01A-11D-A33E-09 TCGA-JY-A6F8-10A-01D-A33H-09 g.chr15:50733646G>T c.205G>T c.(205-207)Gtt>Ttt p.V69F ESCA 15 50774176 50774176 + Frame_Shift_Del DEL A A - TCGA-Z6-A9VB-01A-21D-A37C-09 TCGA-Z6-A9VB-10A-01D-A37F-09 g.chr15:50774176delA c.1717delA c.(1717-1719)aaafs p.K573fs ESCA 15 50784950 50784950 + Missense_Mutation SNP C C T TCGA-LN-A49X-01A-31D-A27G-09 TCGA-LN-A49X-10A-01D-A27G-09 g.chr15:50784950C>T c.2287C>T c.(2287-2289)Cgg>Tgg p.R763W ESCA 15 50784955 50784955 + Missense_Mutation SNP C C A TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr15:50784955C>A c.2292C>A c.(2290-2292)aaC>aaA p.N764K ESCA 15 50785016 50785016 + Missense_Mutation SNP A A G TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr15:50785016A>G c.2353A>G c.(2353-2355)Act>Gct p.T785A ESCA 15 50785054 50785054 + Silent SNP C C T TCGA-LN-A4A2-01A-31D-A27G-09 TCGA-LN-A4A2-10A-01D-A27G-09 g.chr15:50785054C>T c.2391C>T c.(2389-2391)aaC>aaT p.N797N GBM 15 50788098 50788098 + Silent SNP T T C TCGA-14-0862-01B-01D-1845-08 TCGA-14-0862-10C-01D-1845-08 g.chr15:50788098T>C c.2712T>C c.(2710-2712)ttT>ttC p.F904F GBMLGG 15 50769066 50769066 + Silent SNP G G C TCGA-P5-A5F0-01A-11D-A289-08 TCGA-P5-A5F0-10A-01D-A289-08 g.chr15:50769066G>C c.870G>C c.(868-870)ctG>ctC p.L290L GBMLGG 15 50769490 50769490 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:50769490T>C c.1012T>C c.(1012-1014)Tca>Cca p.S338P GBMLGG 15 50784986 50784986 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:50784986G>A c.2323G>A c.(2323-2325)Gct>Act p.A775T GBMLGG 15 50788098 50788098 + Silent SNP T T C TCGA-14-0862-01B-01D-1845-08 TCGA-14-0862-10C-01D-1845-08 g.chr15:50788098T>C c.2712T>C c.(2710-2712)ttT>ttC p.F904F HNSC 15 50733619 50733619 + Missense_Mutation SNP T T G TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr15:50733619T>G c.178T>G c.(178-180)Tat>Gat p.Y60D HNSC 15 50763967 50763967 + Missense_Mutation SNP G G A TCGA-UF-A718-01A-22D-A34J-08 TCGA-UF-A718-10A-01D-A34M-08 g.chr15:50763967G>A c.824G>A c.(823-825)cGg>cAg p.R275Q HNSC 15 50763974 50763974 + Silent SNP G G C TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr15:50763974G>C c.831G>C c.(829-831)ctG>ctC p.L277L HNSC 15 50769168 50769168 + Silent SNP G G A TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr15:50769168G>A c.972G>A c.(970-972)caG>caA p.Q324Q HNSC 15 50769638 50769638 + Missense_Mutation SNP C C G TCGA-CV-6952-01A-11D-1912-08 TCGA-CV-6952-10A-01D-1912-08 g.chr15:50769638C>G c.1160C>G c.(1159-1161)tCt>tGt p.S387C HNSC 15 50773685 50773685 + Missense_Mutation SNP G G T TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr15:50773685G>T c.1226G>T c.(1225-1227)cGt>cTt p.R409L HNSC 15 50773966 50773966 + Missense_Mutation SNP G G C TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chr15:50773966G>C c.1507G>C c.(1507-1509)Gcc>Ccc p.A503P HNSC 15 50774167 50774167 + Missense_Mutation SNP G G C TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr15:50774167G>C c.1708G>C c.(1708-1710)Gat>Cat p.D570H HNSC 15 50784907 50784907 + Missense_Mutation SNP T T G TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr15:50784907T>G c.2244T>G c.(2242-2244)tgT>tgG p.C748W HNSC 15 50784949 50784949 + Silent SNP T T A TCGA-D6-A74Q-01A-11D-A34J-08 TCGA-D6-A74Q-10A-02D-A34M-08 g.chr15:50784949T>A c.2286T>A c.(2284-2286)atT>atA p.I762I HNSC 15 50786338 50786338 + Missense_Mutation SNP G G A TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr15:50786338G>A c.2519G>A c.(2518-2520)gGa>gAa p.G840E HNSC 15 50788043 50788043 + Splice_Site SNP A A T TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr15:50788043A>T c.e17-1 HNSC 15 50788056 50788056 + Silent SNP G G C TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr15:50788056G>C c.2670G>C c.(2668-2670)cgG>cgC p.R890R HNSC 15 50790834 50790834 + Missense_Mutation SNP C C G TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr15:50790834C>G c.3080C>G c.(3079-3081)tCt>tGt p.S1027C HNSC 15 50790857 50790857 + Missense_Mutation SNP C C G TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr15:50790857C>G c.3103C>G c.(3103-3105)Ctt>Gtt p.L1035V HNSC 15 50791262 50791262 + Nonsense_Mutation SNP C C T TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr15:50791262C>T c.3334C>T c.(3334-3336)Cga>Tga p.R1112* KICH 15 50784990 50784990 + Missense_Mutation SNP T T C TCGA-KL-8346-01A-11D-2310-10 TCGA-KL-8346-11A-01D-2310-10 g.chr15:50784990T>C c.2327T>C c.(2326-2328)cTt>cCt p.L776P KIPAN 15 50763851 50763851 + Silent SNP A A G TCGA-BP-4967-01A-01D-1462-08 TCGA-BP-4967-11A-01D-1462-08 g.chr15:50763851A>G c.708A>G c.(706-708)gaA>gaG p.E236E KIPAN 15 50784990 50784990 + Missense_Mutation SNP T T C TCGA-KL-8346-01A-11D-2310-10 TCGA-KL-8346-11A-01D-2310-10 g.chr15:50784990T>C c.2327T>C c.(2326-2328)cTt>cCt p.L776P KIPAN 15 50791105 50791105 + Missense_Mutation SNP C C G TCGA-B0-5080-01A-01D-1501-10 TCGA-B0-5080-11A-01D-1501-10 g.chr15:50791105C>G c.3177C>G c.(3175-3177)caC>caG p.H1059Q KIRC 15 50763851 50763851 + Silent SNP A A G TCGA-BP-4967-01A-01D-1462-08 TCGA-BP-4967-11A-01D-1462-08 g.chr15:50763851A>G c.708A>G c.(706-708)gaA>gaG p.E236E KIRC 15 50791105 50791105 + Missense_Mutation SNP C C G TCGA-B0-5080-01A-01D-1501-10 TCGA-B0-5080-11A-01D-1501-10 g.chr15:50791105C>G c.3177C>G c.(3175-3177)caC>caG p.H1059Q LGG 15 50769066 50769066 + Silent SNP G G C TCGA-P5-A5F0-01A-11D-A289-08 TCGA-P5-A5F0-10A-01D-A289-08 g.chr15:50769066G>C c.870G>C c.(868-870)ctG>ctC p.L290L LGG 15 50769490 50769490 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:50769490T>C c.1012T>C c.(1012-1014)Tca>Cca p.S338P LGG 15 50784986 50784986 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:50784986G>A c.2323G>A c.(2323-2325)Gct>Act p.A775T LIHC 15 50751310 50751310 + Missense_Mutation SNP C C T TCGA-DD-AACZ-01A-11D-A40R-10 TCGA-DD-AACZ-10A-01D-A40U-10 g.chr15:50751310C>T c.449C>T c.(448-450)gCt>gTt p.A150V LIHC 15 50757317 50757317 + Silent SNP A A T TCGA-DD-AAEA-01A-11D-A40R-10 TCGA-DD-AAEA-10A-01D-A40U-10 g.chr15:50757317A>T c.615A>T c.(613-615)cgA>cgT p.R205R LIHC 15 50782610 50782610 + Missense_Mutation SNP A A G TCGA-ED-A459-01A-11D-A25V-10 TCGA-ED-A459-10A-01D-A25V-10 g.chr15:50782610A>G c.2122A>G c.(2122-2124)Agg>Ggg p.R708G LIHC 15 50789394 50789394 + Missense_Mutation SNP A A C TCGA-2Y-A9H9-01A-21D-A38X-10 TCGA-2Y-A9H9-10A-01D-A38X-10 g.chr15:50789394A>C c.3004A>C c.(3004-3006)Aag>Cag p.K1002Q LIHC 15 50789399 50789401 + In_Frame_Del DEL ACC ACC - TCGA-2Y-A9H9-01A-21D-A38X-10 TCGA-2Y-A9H9-10A-01D-A38X-10 g.chr15:50789399_50789401delACC c.3009_3011delACC c.(3007-3012)ttacca>tta p.P1005del LIHC 15 50791193 50791193 + Missense_Mutation SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr15:50791193T>C c.3265T>C c.(3265-3267)Tct>Cct p.S1089P LUAD 15 50741619 50741619 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr15:50741619G>T c.272G>T c.(271-273)gGa>gTa p.G91V LUAD 15 50769116 50769116 + Missense_Mutation SNP G G T TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr15:50769116G>T c.920G>T c.(919-921)tGt>tTt p.C307F LUAD 15 50769167 50769167 + Missense_Mutation SNP A A G TCGA-05-4420-01A-01D-1265-08 TCGA-05-4420-10A-01D-1265-08 g.chr15:50769167A>G c.971A>G c.(970-972)cAg>cGg p.Q324R LUAD 15 50769639 50769639 + Silent SNP T T G TCGA-50-5936-01A-11D-1625-08 TCGA-50-5936-11A-01D-1625-08 g.chr15:50769639T>G c.1161T>G c.(1159-1161)tcT>tcG p.S387S LUAD 15 50773724 50773724 + Missense_Mutation SNP G G C TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr15:50773724G>C c.1265G>C c.(1264-1266)aGa>aCa p.R422T LUAD 15 50774206 50774206 + Nonsense_Mutation SNP A A T TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr15:50774206A>T c.1747A>T c.(1747-1749)Aag>Tag p.K583* LUAD 15 50782020 50782020 + Missense_Mutation SNP G G A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr15:50782020G>A c.1913G>A c.(1912-1914)aGa>aAa p.R638K LUAD 15 50782020 50782020 + Missense_Mutation SNP G G C TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr15:50782020G>C c.1913G>C c.(1912-1914)aGa>aCa p.R638T LUAD 15 50782575 50782575 + Missense_Mutation SNP A A C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr15:50782575A>C c.2087A>C c.(2086-2088)cAt>cCt p.H696P LUAD 15 50789393 50789393 + Nonsense_Mutation SNP G G A TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr15:50789393G>A c.3003G>A c.(3001-3003)tgG>tgA p.W1001* LUAD 15 50791203 50791203 + Missense_Mutation SNP C C G TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr15:50791203C>G c.3275C>G c.(3274-3276)tCc>tGc p.S1092C LUAD 15 50791225 50791225 + Silent SNP A A T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr15:50791225A>T c.3297A>T c.(3295-3297)tcA>tcT p.S1099S LUSC 15 50733609 50733609 + Silent SNP G G A TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr15:50733609G>A c.168G>A c.(166-168)gaG>gaA p.E56E LUSC 15 50757333 50757333 + Missense_Mutation SNP C C G TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr15:50757333C>G c.631C>G c.(631-633)Cag>Gag p.Q211E LUSC 15 50769081 50769081 + Missense_Mutation SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr15:50769081G>T c.885G>T c.(883-885)ttG>ttT p.L295F LUSC 15 50769124 50769124 + Nonsense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:50769124C>T c.928C>T c.(928-930)Cag>Tag p.Q310* LUSC 15 50786304 50786304 + Missense_Mutation SNP G G C TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr15:50786304G>C c.2485G>C c.(2485-2487)Gaa>Caa p.E829Q OV 15 50769603 50769603 + Silent SNP G G A TCGA-42-2582-01A-01D-1526-09 TCGA-42-2582-10A-01D-1526-09 g.chr15:50769603G>A c.1125G>A c.(1123-1125)ctG>ctA p.L375L PAAD 15 50741645 50741645 + Frame_Shift_Del DEL G G - TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr15:50741645delG c.298delG c.(298-300)gaafs p.E101fs PAAD 15 50782531 50782531 + Silent SNP G G A TCGA-2L-AAQE-01A-11D-A397-08 TCGA-2L-AAQE-11A-11D-A39A-08 g.chr15:50782531G>A c.2043G>A c.(2041-2043)ccG>ccA p.P681P PAAD 15 50782713 50782713 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:50782713G>A c.2225G>A c.(2224-2226)cGg>cAg p.R742Q PAAD 15 50786282 50786282 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:50786282G>A c.2463G>A c.(2461-2463)ggG>ggA p.G821G PAAD 15 50788095 50788095 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:50788095C>T c.2709C>T c.(2707-2709)gaC>gaT p.D903D PRAD 15 50782019 50782019 + Missense_Mutation SNP A A G TCGA-J9-A8CP-01A-11D-A34U-08 TCGA-J9-A8CP-10A-01D-A34X-08 g.chr15:50782019A>G c.1912A>G c.(1912-1914)Aga>Gga p.R638G PRAD 15 50788105 50788105 + Missense_Mutation SNP G G T TCGA-QU-A6IN-01A-11D-A31L-08 TCGA-QU-A6IN-10A-01D-A31J-08 g.chr15:50788105G>T c.2719G>T c.(2719-2721)Gca>Tca p.A907S PRAD 15 50790907 50790907 + Silent SNP T T C TCGA-HC-8261-01A-11D-2260-08 TCGA-HC-8261-10A-01D-2260-08 g.chr15:50790907T>C c.3153T>C c.(3151-3153)taT>taC p.Y1051Y READ 15 50773953 50773953 + Silent SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:50773953A>G c.1494A>G c.(1492-1494)gaA>gaG p.E498E READ 15 50782647 50782647 + Missense_Mutation SNP C C A TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr15:50782647C>A c.2159C>A c.(2158-2160)cCa>cAa p.P720Q READ 15 50784958 50784958 + Silent SNP C C A TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr15:50784958C>A c.2295C>A c.(2293-2295)ctC>ctA p.L765L READ 15 50786372 50786372 + Missense_Mutation SNP A A C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:50786372A>C c.2553A>C c.(2551-2553)aaA>aaC p.K851N SARC 15 50784950 50784950 + Missense_Mutation SNP C C T TCGA-Z4-A9VC-01A-11D-A37C-09 TCGA-Z4-A9VC-10A-01D-A37F-09 g.chr15:50784950C>T c.2287C>T c.(2287-2289)Cgg>Tgg p.R763W SARC 15 50784955 50784955 + Missense_Mutation SNP C C A TCGA-Z4-A9VC-01A-11D-A37C-09 TCGA-Z4-A9VC-10A-01D-A37F-09 g.chr15:50784955C>A c.2292C>A c.(2290-2292)aaC>aaA p.N764K SKCM 15 50733667 50733667 + Nonsense_Mutation SNP A A T TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr15:50733667A>T c.226A>T c.(226-228)Aga>Tga p.R76* SKCM 15 50741605 50741605 + Silent SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr15:50741605C>T c.258C>T c.(256-258)ttC>ttT p.F86F SKCM 15 50774163 50774163 + Silent SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:50774163A>C c.1704A>C c.(1702-1704)gtA>gtC p.V568V SKCM 15 50774164 50774164 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:50774164G>A c.1705G>A c.(1705-1707)Gaa>Aaa p.E569K SKCM 15 50782062 50782062 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:50782062C>T c.1955C>T c.(1954-1956)cCt>cTt p.P652L SKCM 15 50782595 50782595 + Missense_Mutation SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr15:50782595C>T c.2107C>T c.(2107-2109)Cct>Tct p.P703S SKCM 15 50782595 50782595 + Missense_Mutation SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr15:50782595C>T c.2107C>T c.(2107-2109)Cct>Tct p.P703S SKCM 15 50785001 50785001 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:50785001C>T c.2338C>T c.(2338-2340)Cgt>Tgt p.R780C SKCM 15 50786292 50786292 + Missense_Mutation SNP G G A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr15:50786292G>A c.2473G>A c.(2473-2475)Gaa>Aaa p.E825K SKCM 15 50786354 50786354 + Silent SNP C C T TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr15:50786354C>T c.2535C>T c.(2533-2535)atC>atT p.I845I SKCM 15 50786460 50786460 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr15:50786460C>G c.2641C>G c.(2641-2643)Cat>Gat p.H881D SKCM 15 50788176 50788176 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:50788176C>T c.2790C>T c.(2788-2790)ttC>ttT p.F930F SKCM 15 50791221 50791221 + Missense_Mutation SNP C C T TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr15:50791221C>T c.3293C>T c.(3292-3294)tCt>tTt p.S1098F

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 50782647 50782647 single base substitution C G downstream_gene_variant BLCA-CN 15 50782647 50782647 single base substitution C G missense_variant P614R 1841C>G BLCA-CN 15 50782647 50782647 single base substitution C G missense_variant P720R 2159C>G BLCA-CN 15 50782647 50782647 single base substitution C G upstream_gene_variant BLCA-US 15 50757369 50757369 single base substitution G A 3_prime_UTR_variant BLCA-US 15 50757369 50757369 single base substitution G A downstream_gene_variant BLCA-US 15 50757369 50757369 single base substitution G A exon_variant BLCA-US 15 50757369 50757369 single base substitution G A intron_variant BLCA-US 15 50757369 50757369 single base substitution G A missense_variant E146K 436G>A BLCA-US 15 50757369 50757369 single base substitution G A missense_variant E223K 667G>A BLCA-US 15 50769684 50769684 single base substitution G A 3_prime_UTR_variant BLCA-US 15 50769684 50769684 single base substitution G A exon_variant BLCA-US 15 50769684 50769684 single base substitution G A synonymous_variant K325K 975G>A BLCA-US 15 50769684 50769684 single base substitution G A synonymous_variant K402K 1206G>A BLCA-US 15 50776527 50776527 single base substitution G A downstream_gene_variant BLCA-US 15 50776527 50776527 single base substitution G A intron_variant BLCA-US 15 50776527 50776527 single base substitution G A missense_variant R620K 1859G>A BLCA-US 15 50782585 50782585 single base substitution G C exon_variant BLCA-US 15 50782585 50782585 single base substitution G C missense_variant K593N 1779G>C BLCA-US 15 50782585 50782585 single base substitution G C missense_variant K699N 2097G>C BLCA-US 15 50782585 50782585 single base substitution G C upstream_gene_variant BLCA-US 15 50782647 50782647 single base substitution C A downstream_gene_variant BLCA-US 15 50782647 50782647 single base substitution C A missense_variant P614Q 1841C>A BLCA-US 15 50782647 50782647 single base substitution C A missense_variant P720Q 2159C>A BLCA-US 15 50782647 50782647 single base substitution C A upstream_gene_variant BLCA-US 15 50784944 50784944 single base substitution C G downstream_gene_variant BLCA-US 15 50784944 50784944 single base substitution C G missense_variant Q655E 1963C>G BLCA-US 15 50784944 50784944 single base substitution C G missense_variant Q761E 2281C>G BLCA-US 15 50784944 50784944 single base substitution C G upstream_gene_variant BOCA-FR 15 50717866 50717866 single base substitution A C intron_variant BOCA-FR 15 50717866 50717866 single base substitution A C upstream_gene_variant BRCA-EU 15 50712789 50712789 single base substitution A G upstream_gene_variant BRCA-EU 15 50713060 50713060 single base substitution G C upstream_gene_variant BRCA-EU 15 50713189 50713189 single base substitution A C upstream_gene_variant BRCA-EU 15 50714602 50714602 single base substitution T C upstream_gene_variant BRCA-EU 15 50714893 50714893 single base substitution C G upstream_gene_variant BRCA-EU 15 50715559 50715559 single base substitution C A upstream_gene_variant BRCA-EU 15 50717184 50717184 single base substitution A T intron_variant BRCA-EU 15 50717184 50717184 single base substitution A T upstream_gene_variant BRCA-EU 15 50717977 50717977 deletion of <=200bp T - intron_variant BRCA-EU 15 50717977 50717977 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 50719311 50719311 deletion of <=200bp T - intron_variant BRCA-EU 15 50720579 50720579 single base substitution G A intron_variant BRCA-EU 15 50721097 50721097 single base substitution G A intron_variant BRCA-EU 15 50723692 50723692 insertion of <=200bp - T intron_variant BRCA-EU 15 50723790 50723790 single base substitution G T intron_variant BRCA-EU 15 50724451 50724451 single base substitution T A intron_variant BRCA-EU 15 50724549 50724549 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 15 50724549 50724549 single base substitution C G intron_variant BRCA-EU 15 50726181 50726181 insertion of <=200bp - TCTTTA intron_variant BRCA-EU 15 50727013 50727013 single base substitution C T intron_variant BRCA-EU 15 50727013 50727013 single base substitution C T upstream_gene_variant BRCA-EU 15 50728391 50728391 deletion of <=200bp T - intron_variant BRCA-EU 15 50728391 50728391 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 50729149 50729149 single base substitution G A intron_variant BRCA-EU 15 50729149 50729149 single base substitution G A upstream_gene_variant BRCA-EU 15 50729151 50729151 single base substitution G A intron_variant BRCA-EU 15 50729151 50729151 single base substitution G A upstream_gene_variant BRCA-EU 15 50729498 50729498 single base substitution A G intron_variant BRCA-EU 15 50729498 50729498 single base substitution A G upstream_gene_variant BRCA-EU 15 50729888 50729888 single base substitution T C intron_variant BRCA-EU 15 50729888 50729888 single base substitution T C upstream_gene_variant BRCA-EU 15 50730686 50730686 single base substitution G C intron_variant BRCA-EU 15 50730686 50730686 single base substitution G C upstream_gene_variant BRCA-EU 15 50732444 50732444 single base substitution A G intron_variant BRCA-EU 15 50732511 50732511 single base substitution A G intron_variant BRCA-EU 15 50734020 50734020 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 50734020 50734020 deletion of <=200bp T - intron_variant BRCA-EU 15 50734423 50734423 single base substitution G A downstream_gene_variant BRCA-EU 15 50734423 50734423 single base substitution G A intron_variant BRCA-EU 15 50734765 50734765 single base substitution A G downstream_gene_variant BRCA-EU 15 50734765 50734765 single base substitution A G intron_variant BRCA-EU 15 50734848 50734848 single base substitution A G downstream_gene_variant BRCA-EU 15 50734848 50734848 single base substitution A G intron_variant BRCA-EU 15 50734909 50734909 single base substitution T C downstream_gene_variant BRCA-EU 15 50734909 50734909 single base substitution T C intron_variant BRCA-EU 15 50737344 50737344 single base substitution A G downstream_gene_variant BRCA-EU 15 50737344 50737344 single base substitution A G intron_variant BRCA-EU 15 50739594 50739594 single base substitution C T downstream_gene_variant BRCA-EU 15 50739594 50739594 single base substitution C T intron_variant BRCA-EU 15 50741897 50741897 single base substitution A G downstream_gene_variant BRCA-EU 15 50741897 50741897 single base substitution A G intron_variant BRCA-EU 15 50742207 50742207 single base substitution C T downstream_gene_variant BRCA-EU 15 50742207 50742207 single base substitution C T intron_variant BRCA-EU 15 50742556 50742556 insertion of <=200bp - A downstream_gene_variant BRCA-EU 15 50742556 50742556 insertion of <=200bp - A intron_variant BRCA-EU 15 50745625 50745625 single base substitution A C downstream_gene_variant BRCA-EU 15 50745625 50745625 single base substitution A C intron_variant BRCA-EU 15 50745871 50745871 single base substitution G T downstream_gene_variant BRCA-EU 15 50745871 50745871 single base substitution G T intron_variant BRCA-EU 15 50745871 50745871 single base substitution G T upstream_gene_variant BRCA-EU 15 50748039 50748053 deletion of <=200bp GCAATTTGGGCAAGT - intron_variant BRCA-EU 15 50748039 50748053 deletion of <=200bp GCAATTTGGGCAAGT - upstream_gene_variant BRCA-EU 15 50748104 50748104 single base substitution G T intron_variant BRCA-EU 15 50748104 50748104 single base substitution G T upstream_gene_variant BRCA-EU 15 50749321 50749321 single base substitution G C intron_variant BRCA-EU 15 50749321 50749321 single base substitution G C upstream_gene_variant BRCA-EU 15 50749631 50749631 single base substitution G A intron_variant BRCA-EU 15 50749631 50749631 single base substitution G A upstream_gene_variant BRCA-EU 15 50750374 50750374 single base substitution A G intron_variant BRCA-EU 15 50750374 50750374 single base substitution A G upstream_gene_variant BRCA-EU 15 50750545 50750545 single base substitution A G intron_variant BRCA-EU 15 50750545 50750545 single base substitution A G upstream_gene_variant BRCA-EU 15 50751508 50751508 single base substitution C T downstream_gene_variant BRCA-EU 15 50751508 50751508 single base substitution C T intron_variant BRCA-EU 15 50751616 50751616 single base substitution A G downstream_gene_variant BRCA-EU 15 50751616 50751616 single base substitution A G intron_variant BRCA-EU 15 50751782 50751782 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 50751782 50751782 deletion of <=200bp A - intron_variant BRCA-EU 15 50752279 50752279 single base substitution C T downstream_gene_variant BRCA-EU 15 50752279 50752279 single base substitution C T intron_variant BRCA-EU 15 50756506 50756506 single base substitution A G downstream_gene_variant BRCA-EU 15 50756506 50756506 single base substitution A G intron_variant BRCA-EU 15 50758113 50758113 single base substitution G A downstream_gene_variant BRCA-EU 15 50758113 50758113 single base substitution G A intron_variant BRCA-EU 15 50759841 50759841 single base substitution C T downstream_gene_variant BRCA-EU 15 50759841 50759841 single base substitution C T intron_variant BRCA-EU 15 50760600 50760600 single base substitution C T downstream_gene_variant BRCA-EU 15 50760600 50760600 single base substitution C T intron_variant BRCA-EU 15 50763405 50763405 single base substitution G A intron_variant BRCA-EU 15 50764559 50764559 single base substitution G A downstream_gene_variant BRCA-EU 15 50764559 50764559 single base substitution G A intron_variant BRCA-EU 15 50765642 50765642 single base substitution G C downstream_gene_variant BRCA-EU 15 50765642 50765642 single base substitution G C intron_variant BRCA-EU 15 50769508 50769508 single base substitution C A 3_prime_UTR_variant BRCA-EU 15 50769508 50769508 single base substitution C A exon_variant BRCA-EU 15 50769508 50769508 single base substitution C A missense_variant P267T 799C>A BRCA-EU 15 50769508 50769508 single base substitution C A missense_variant P344T 1030C>A BRCA-EU 15 50770050 50770050 deletion of <=200bp G - intron_variant BRCA-EU 15 50770165 50770165 single base substitution C T intron_variant BRCA-EU 15 50771041 50771041 single base substitution C T intron_variant BRCA-EU 15 50772325 50772325 single base substitution G A intron_variant BRCA-EU 15 50775513 50775513 single base substitution C T downstream_gene_variant BRCA-EU 15 50775513 50775513 single base substitution C T intron_variant BRCA-EU 15 50777521 50777521 single base substitution C T downstream_gene_variant BRCA-EU 15 50777521 50777521 single base substitution C T intron_variant BRCA-EU 15 50777521 50777521 single base substitution C T upstream_gene_variant BRCA-EU 15 50777801 50777801 single base substitution C G downstream_gene_variant BRCA-EU 15 50777801 50777801 single base substitution C G intron_variant BRCA-EU 15 50777801 50777801 single base substitution C G upstream_gene_variant BRCA-EU 15 50778527 50778527 single base substitution T C downstream_gene_variant BRCA-EU 15 50778527 50778527 single base substitution T C intron_variant BRCA-EU 15 50778527 50778527 single base substitution T C upstream_gene_variant BRCA-EU 15 50778673 50778673 single base substitution G A downstream_gene_variant BRCA-EU 15 50778673 50778673 single base substitution G A intron_variant BRCA-EU 15 50778673 50778673 single base substitution G A upstream_gene_variant BRCA-EU 15 50779433 50779433 single base substitution G A intron_variant BRCA-EU 15 50779433 50779433 single base substitution G A upstream_gene_variant BRCA-EU 15 50780548 50780548 single base substitution G C intron_variant BRCA-EU 15 50780548 50780548 single base substitution G C upstream_gene_variant BRCA-EU 15 50781023 50781023 single base substitution G A intron_variant BRCA-EU 15 50781023 50781023 single base substitution G A upstream_gene_variant BRCA-EU 15 50781315 50781315 single base substitution C G intron_variant BRCA-EU 15 50781315 50781315 single base substitution C G upstream_gene_variant BRCA-EU 15 50781331 50781331 single base substitution G A intron_variant BRCA-EU 15 50781331 50781331 single base substitution G A upstream_gene_variant BRCA-EU 15 50782347 50782347 single base substitution G A intron_variant BRCA-EU 15 50782347 50782347 single base substitution G A upstream_gene_variant BRCA-EU 15 50783399 50783399 single base substitution G A downstream_gene_variant BRCA-EU 15 50783399 50783399 single base substitution G A intron_variant BRCA-EU 15 50783399 50783399 single base substitution G A upstream_gene_variant BRCA-EU 15 50783807 50783807 single base substitution C G downstream_gene_variant BRCA-EU 15 50783807 50783807 single base substitution C G intron_variant BRCA-EU 15 50783807 50783807 single base substitution C G upstream_gene_variant BRCA-EU 15 50785078 50785078 single base substitution C G downstream_gene_variant BRCA-EU 15 50785078 50785078 single base substitution C G missense_variant F699L 2097C>G BRCA-EU 15 50785078 50785078 single base substitution C G missense_variant F805L 2415C>G BRCA-EU 15 50785078 50785078 single base substitution C G upstream_gene_variant BRCA-EU 15 50785268 50785268 single base substitution G C downstream_gene_variant BRCA-EU 15 50785268 50785268 single base substitution G C intron_variant BRCA-EU 15 50785268 50785268 single base substitution G C upstream_gene_variant BRCA-EU 15 50785874 50785874 single base substitution C G downstream_gene_variant BRCA-EU 15 50785874 50785874 single base substitution C G exon_variant BRCA-EU 15 50785874 50785874 single base substitution C G intron_variant BRCA-EU 15 50785874 50785874 single base substitution C G upstream_gene_variant BRCA-EU 15 50787185 50787185 single base substitution C A downstream_gene_variant BRCA-EU 15 50787185 50787185 single base substitution C A intron_variant BRCA-EU 15 50787185 50787185 single base substitution C A upstream_gene_variant BRCA-EU 15 50787759 50787759 single base substitution A G intron_variant BRCA-EU 15 50787759 50787759 single base substitution A G upstream_gene_variant BRCA-EU 15 50788714 50788714 single base substitution C T intron_variant BRCA-EU 15 50788714 50788714 single base substitution C T upstream_gene_variant BRCA-EU 15 50789932 50789932 single base substitution C T intron_variant BRCA-EU 15 50789932 50789932 single base substitution C T upstream_gene_variant BRCA-EU 15 50793707 50793707 single base substitution T C downstream_gene_variant BRCA-EU 15 50794367 50794367 single base substitution C A downstream_gene_variant BRCA-EU 15 50795756 50795756 single base substitution C T downstream_gene_variant BRCA-EU 15 50797172 50797172 single base substitution C T downstream_gene_variant BRCA-FR 15 50713189 50713189 single base substitution A C upstream_gene_variant BRCA-FR 15 50721097 50721097 single base substitution G A intron_variant BRCA-FR 15 50729149 50729149 single base substitution G A intron_variant BRCA-FR 15 50729149 50729149 single base substitution G A upstream_gene_variant BRCA-FR 15 50729151 50729151 single base substitution G A intron_variant BRCA-FR 15 50729151 50729151 single base substitution G A upstream_gene_variant BRCA-FR 15 50736878 50736878 single base substitution C T downstream_gene_variant BRCA-FR 15 50736878 50736878 single base substitution C T intron_variant BRCA-FR 15 50751616 50751616 single base substitution A G downstream_gene_variant BRCA-FR 15 50751616 50751616 single base substitution A G intron_variant BRCA-FR 15 50759841 50759841 single base substitution C T downstream_gene_variant BRCA-FR 15 50759841 50759841 single base substitution C T intron_variant BRCA-FR 15 50772825 50772825 single base substitution G C intron_variant BRCA-FR 15 50775513 50775513 single base substitution C T downstream_gene_variant BRCA-FR 15 50775513 50775513 single base substitution C T intron_variant BRCA-FR 15 50785078 50785078 single base substitution C G downstream_gene_variant BRCA-FR 15 50785078 50785078 single base substitution C G missense_variant F699L 2097C>G BRCA-FR 15 50785078 50785078 single base substitution C G missense_variant F805L 2415C>G BRCA-FR 15 50785078 50785078 single base substitution C G upstream_gene_variant BRCA-FR 15 50794339 50794339 single base substitution C T downstream_gene_variant BRCA-UK 15 50763590 50763590 single base substitution C T intron_variant BRCA-UK 15 50767170 50767170 single base substitution A G downstream_gene_variant BRCA-UK 15 50767170 50767170 single base substitution A G intron_variant BRCA-US 15 50741617 50741617 single base substitution T G downstream_gene_variant BRCA-US 15 50741617 50741617 single base substitution T G exon_variant BRCA-US 15 50741617 50741617 single base substitution T G intron_variant BRCA-US 15 50741617 50741617 single base substitution T G synonymous_variant L90L 270T>G BRCA-US 15 50751285 50751285 single base substitution G A 3_prime_UTR_variant BRCA-US 15 50751285 50751285 single base substitution G A downstream_gene_variant BRCA-US 15 50751285 50751285 single base substitution G A exon_variant BRCA-US 15 50751285 50751285 single base substitution G A intron_variant BRCA-US 15 50751285 50751285 single base substitution G A missense_variant G142R 424G>A BRCA-US 15 50751285 50751285 single base substitution G A missense_variant G65R 193G>A BRCA-US 15 50769138 50769138 single base substitution T C 3_prime_UTR_variant BRCA-US 15 50769138 50769138 single base substitution T C exon_variant BRCA-US 15 50769138 50769138 single base substitution T C intron_variant BRCA-US 15 50769138 50769138 single base substitution T C synonymous_variant N237N 711T>C BRCA-US 15 50769138 50769138 single base substitution T C synonymous_variant N314N 942T>C BRCA-US 15 50773883 50773883 single base substitution A C 3_prime_UTR_variant BRCA-US 15 50773883 50773883 single base substitution A C exon_variant BRCA-US 15 50773883 50773883 single base substitution A C missense_variant K398T 1193A>C BRCA-US 15 50773883 50773883 single base substitution A C missense_variant K475T 1424A>C BRCA-US 15 50773900 50773900 single base substitution G T 3_prime_UTR_variant BRCA-US 15 50773900 50773900 single base substitution G T downstream_gene_variant BRCA-US 15 50773900 50773900 single base substitution G T stop_gained E404* 1210G>T BRCA-US 15 50773900 50773900 single base substitution G T stop_gained E481* 1441G>T BRCA-US 15 50782481 50782481 single base substitution A C exon_variant BRCA-US 15 50782481 50782481 single base substitution A C missense_variant T559P 1675A>C BRCA-US 15 50782481 50782481 single base substitution A C missense_variant T665P 1993A>C BRCA-US 15 50782481 50782481 single base substitution A C upstream_gene_variant BRCA-US 15 50782646 50782646 single base substitution C G downstream_gene_variant BRCA-US 15 50782646 50782646 single base substitution C G missense_variant P614A 1840C>G BRCA-US 15 50782646 50782646 single base substitution C G missense_variant P720A 2158C>G BRCA-US 15 50782646 50782646 single base substitution C G upstream_gene_variant BRCA-US 15 50784950 50784950 single base substitution C T downstream_gene_variant BRCA-US 15 50784950 50784950 single base substitution C T missense_variant R657W 1969C>T BRCA-US 15 50784950 50784950 single base substitution C T missense_variant R763W 2287C>T BRCA-US 15 50784950 50784950 single base substitution C T upstream_gene_variant BRCA-US 15 50784955 50784955 single base substitution C A downstream_gene_variant BRCA-US 15 50784955 50784955 single base substitution C A missense_variant N658K 1974C>A BRCA-US 15 50784955 50784955 single base substitution C A missense_variant N764K 2292C>A BRCA-US 15 50784955 50784955 single base substitution C A upstream_gene_variant BRCA-US 15 50786430 50786430 single base substitution G C downstream_gene_variant BRCA-US 15 50786430 50786430 single base substitution G C exon_variant BRCA-US 15 50786430 50786430 single base substitution G C missense_variant E765Q 2293G>C BRCA-US 15 50786430 50786430 single base substitution G C missense_variant E871Q 2611G>C BRCA-US 15 50786430 50786430 single base substitution G C upstream_gene_variant BTCA-JP 15 50731525 50731525 single base substitution T G intron_variant BTCA-JP 15 50741716 50741716 single base substitution A C downstream_gene_variant BTCA-JP 15 50741716 50741716 single base substitution A C intron_variant BTCA-JP 15 50754346 50754346 insertion of <=200bp - T downstream_gene_variant BTCA-JP 15 50754346 50754346 insertion of <=200bp - T intron_variant BTCA-JP 15 50785083 50785083 single base substitution G A downstream_gene_variant BTCA-JP 15 50785083 50785083 single base substitution G A missense_variant R701Q 2102G>A BTCA-JP 15 50785083 50785083 single base substitution G A missense_variant R807Q 2420G>A BTCA-JP 15 50785083 50785083 single base substitution G A upstream_gene_variant BTCA-JP 15 50788116 50788116 single base substitution C A exon_variant BTCA-JP 15 50788116 50788116 single base substitution C A synonymous_variant A804A 2412C>A BTCA-JP 15 50788116 50788116 single base substitution C A synonymous_variant A910A 2730C>A BTCA-JP 15 50788116 50788116 single base substitution C A upstream_gene_variant CESC-US 15 50741664 50741664 single base substitution C G downstream_gene_variant CESC-US 15 50741664 50741664 single base substitution C G exon_variant CESC-US 15 50741664 50741664 single base substitution C G intron_variant CESC-US 15 50741664 50741664 single base substitution C G missense_variant S106C 317C>G CESC-US 15 50751336 50751336 single base substitution G C 3_prime_UTR_variant CESC-US 15 50751336 50751336 single base substitution G C downstream_gene_variant CESC-US 15 50751336 50751336 single base substitution G C exon_variant CESC-US 15 50751336 50751336 single base substitution G C intron_variant CESC-US 15 50751336 50751336 single base substitution G C missense_variant D159H 475G>C CESC-US 15 50751336 50751336 single base substitution G C missense_variant D82H 244G>C CESC-US 15 50776513 50776513 single base substitution G A downstream_gene_variant CESC-US 15 50776513 50776513 single base substitution G A intron_variant CESC-US 15 50776513 50776513 single base substitution G A synonymous_variant R615R 1845G>A CESC-US 15 50782647 50782647 single base substitution C A downstream_gene_variant CESC-US 15 50782647 50782647 single base substitution C A missense_variant P614Q 1841C>A CESC-US 15 50782647 50782647 single base substitution C A missense_variant P720Q 2159C>A CESC-US 15 50782647 50782647 single base substitution C A upstream_gene_variant CESC-US 15 50785054 50785054 single base substitution C T downstream_gene_variant CESC-US 15 50785054 50785054 single base substitution C T synonymous_variant N691N 2073C>T CESC-US 15 50785054 50785054 single base substitution C T synonymous_variant N797N 2391C>T CESC-US 15 50785054 50785054 single base substitution C T upstream_gene_variant CESC-US 15 50786321 50786321 single base substitution G T downstream_gene_variant CESC-US 15 50786321 50786321 single base substitution G T exon_variant CESC-US 15 50786321 50786321 single base substitution G T missense_variant M728I 2184G>T CESC-US 15 50786321 50786321 single base substitution G T missense_variant M834I 2502G>T CESC-US 15 50786321 50786321 single base substitution G T upstream_gene_variant CESC-US 15 50788052 50788052 single base substitution A C exon_variant CESC-US 15 50788052 50788052 single base substitution A C missense_variant N783T 2348A>C CESC-US 15 50788052 50788052 single base substitution A C missense_variant N889T 2666A>C CESC-US 15 50788052 50788052 single base substitution A C upstream_gene_variant CESC-US 15 50789248 50789248 single base substitution G A intron_variant CESC-US 15 50789248 50789248 single base substitution G A upstream_gene_variant CLLE-ES 15 50765742 50765742 single base substitution A T downstream_gene_variant CLLE-ES 15 50765742 50765742 single base substitution A T intron_variant CLLE-ES 15 50783793 50783793 single base substitution T C downstream_gene_variant CLLE-ES 15 50783793 50783793 single base substitution T C intron_variant CLLE-ES 15 50783793 50783793 single base substitution T C upstream_gene_variant CLLE-ES 15 50796744 50796744 single base substitution G A downstream_gene_variant COAD-US 15 50731368 50731368 single base substitution C A exon_variant COAD-US 15 50731368 50731368 single base substitution C A intron_variant COAD-US 15 50731368 50731368 single base substitution C A missense_variant T33N 98C>A COAD-US 15 50733660 50733660 insertion of <=200bp - A exon_variant COAD-US 15 50733660 50733660 insertion of <=200bp - A frameshift_variant I73I? COAD-US 15 50733660 50733660 insertion of <=200bp - A intron_variant COAD-US 15 50763915 50763915 single base substitution C T 3_prime_UTR_variant COAD-US 15 50763915 50763915 single base substitution C T exon_variant COAD-US 15 50763915 50763915 single base substitution C T intron_variant COAD-US 15 50763915 50763915 single base substitution C T missense_variant L181F 541C>T COAD-US 15 50763915 50763915 single base substitution C T missense_variant L258F 772C>T COAD-US 15 50773954 50773954 single base substitution C T downstream_gene_variant COAD-US 15 50773954 50773954 single base substitution C T stop_gained Q422* 1264C>T COAD-US 15 50773954 50773954 single base substitution C T stop_gained Q499* 1495C>T COAD-US 15 50782025 50782025 single base substitution C T exon_variant COAD-US 15 50782025 50782025 single base substitution C T stop_gained R534* 1600C>T COAD-US 15 50782025 50782025 single base substitution C T stop_gained R640* 1918C>T COAD-US 15 50782025 50782025 single base substitution C T upstream_gene_variant COAD-US 15 50785016 50785016 single base substitution A G downstream_gene_variant COAD-US 15 50785016 50785016 single base substitution A G missense_variant T679A 2035A>G COAD-US 15 50785016 50785016 single base substitution A G missense_variant T785A 2353A>G COAD-US 15 50785016 50785016 single base substitution A G upstream_gene_variant COAD-US 15 50789322 50789322 single base substitution A C exon_variant COAD-US 15 50789322 50789322 single base substitution A C missense_variant T872P 2614A>C COAD-US 15 50789322 50789322 single base substitution A C missense_variant T978P 2932A>C COAD-US 15 50789322 50789322 single base substitution A C upstream_gene_variant COAD-US 15 50789375 50789375 deletion of <=200bp A - exon_variant COAD-US 15 50789375 50789375 deletion of <=200bp A - frameshift_variant L889 COAD-US 15 50789375 50789375 deletion of <=200bp A - frameshift_variant L995 COAD-US 15 50789375 50789375 deletion of <=200bp A - upstream_gene_variant COAD-US 15 50793007 50793007 single base substitution G T 3_prime_UTR_variant COAD-US 15 50793007 50793007 single base substitution G T downstream_gene_variant COCA-CN 15 50731526 50731526 single base substitution C T intron_variant COCA-CN 15 50757198 50757198 single base substitution T C downstream_gene_variant COCA-CN 15 50757198 50757198 single base substitution T C intron_variant COCA-CN 15 50785083 50785083 single base substitution G A downstream_gene_variant COCA-CN 15 50785083 50785083 single base substitution G A missense_variant R701Q 2102G>A COCA-CN 15 50785083 50785083 single base substitution G A missense_variant R807Q 2420G>A COCA-CN 15 50785083 50785083 single base substitution G A upstream_gene_variant COCA-CN 15 50785570 50785570 single base substitution G T downstream_gene_variant COCA-CN 15 50785570 50785570 single base substitution G T exon_variant COCA-CN 15 50785570 50785570 single base substitution G T intron_variant COCA-CN 15 50793089 50793089 single base substitution G A 3_prime_UTR_variant COCA-CN 15 50793089 50793089 single base substitution G A downstream_gene_variant ESAD-UK 15 50712510 50712510 single base substitution A G upstream_gene_variant ESAD-UK 15 50713998 50713998 single base substitution G T upstream_gene_variant ESAD-UK 15 50714667 50714667 single base substitution G A upstream_gene_variant ESAD-UK 15 50715429 50715429 single base substitution T A upstream_gene_variant ESAD-UK 15 50718326 50718326 single base substitution A G intron_variant ESAD-UK 15 50718326 50718326 single base substitution A G upstream_gene_variant ESAD-UK 15 50718358 50718358 single base substitution A C intron_variant ESAD-UK 15 50718358 50718358 single base substitution A C upstream_gene_variant ESAD-UK 15 50718451 50718451 single base substitution C T intron_variant ESAD-UK 15 50718451 50718451 single base substitution C T upstream_gene_variant ESAD-UK 15 50719311 50719311 single base substitution T C intron_variant ESAD-UK 15 50719937 50719937 single base substitution G C intron_variant ESAD-UK 15 50724840 50724840 single base substitution T A intron_variant ESAD-UK 15 50725264 50725264 deletion of <=200bp C - intron_variant ESAD-UK 15 50726403 50726403 single base substitution G A intron_variant ESAD-UK 15 50726403 50726403 single base substitution G A upstream_gene_variant ESAD-UK 15 50735675 50735675 deletion of <=200bp T - downstream_gene_variant ESAD-UK 15 50735675 50735675 deletion of <=200bp T - intron_variant ESAD-UK 15 50735836 50735836 single base substitution A G downstream_gene_variant ESAD-UK 15 50735836 50735836 single base substitution A G intron_variant ESAD-UK 15 50736457 50736457 single base substitution C T downstream_gene_variant ESAD-UK 15 50736457 50736457 single base substitution C T intron_variant ESAD-UK 15 50740989 50740989 single base substitution T C downstream_gene_variant ESAD-UK 15 50740989 50740989 single base substitution T C intron_variant ESAD-UK 15 50744866 50744866 deletion of <=200bp T - downstream_gene_variant ESAD-UK 15 50744866 50744866 deletion of <=200bp T - intron_variant ESAD-UK 15 50747233 50747233 single base substitution G T intron_variant ESAD-UK 15 50747233 50747233 single base substitution G T upstream_gene_variant ESAD-UK 15 50747532 50747532 single base substitution C T intron_variant ESAD-UK 15 50747532 50747532 single base substitution C T upstream_gene_variant ESAD-UK 15 50748897 50748897 single base substitution A C intron_variant ESAD-UK 15 50748897 50748897 single base substitution A C upstream_gene_variant ESAD-UK 15 50754838 50754838 single base substitution G A downstream_gene_variant ESAD-UK 15 50754838 50754838 single base substitution G A intron_variant ESAD-UK 15 50756659 50756659 single base substitution G A downstream_gene_variant ESAD-UK 15 50756659 50756659 single base substitution G A intron_variant ESAD-UK 15 50758651 50758651 single base substitution G A downstream_gene_variant ESAD-UK 15 50758651 50758651 single base substitution G A intron_variant ESAD-UK 15 50764558 50764558 single base substitution T G downstream_gene_variant ESAD-UK 15 50764558 50764558 single base substitution T G intron_variant ESAD-UK 15 50766015 50766015 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 50766015 50766015 deletion of <=200bp A - intron_variant ESAD-UK 15 50768287 50768287 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 50768287 50768287 deletion of <=200bp A - intron_variant ESAD-UK 15 50771543 50771543 single base substitution C T intron_variant ESAD-UK 15 50771743 50771743 single base substitution G C intron_variant ESAD-UK 15 50773849 50773849 single base substitution C T 3_prime_UTR_variant ESAD-UK 15 50773849 50773849 single base substitution C T exon_variant ESAD-UK 15 50773849 50773849 single base substitution C T missense_variant R387C 1159C>T ESAD-UK 15 50773849 50773849 single base substitution C T missense_variant R464C 1390C>T ESAD-UK 15 50775768 50775768 single base substitution G A downstream_gene_variant ESAD-UK 15 50775768 50775768 single base substitution G A intron_variant ESAD-UK 15 50776588 50776588 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 50776588 50776588 deletion of <=200bp A - intron_variant ESAD-UK 15 50777388 50777388 single base substitution G A downstream_gene_variant ESAD-UK 15 50777388 50777388 single base substitution G A intron_variant ESAD-UK 15 50777388 50777388 single base substitution G A upstream_gene_variant ESAD-UK 15 50778742 50778742 single base substitution T G downstream_gene_variant ESAD-UK 15 50778742 50778742 single base substitution T G intron_variant ESAD-UK 15 50778742 50778742 single base substitution T G upstream_gene_variant ESAD-UK 15 50779324 50779324 single base substitution A G intron_variant ESAD-UK 15 50779324 50779324 single base substitution A G upstream_gene_variant ESAD-UK 15 50779326 50779326 single base substitution A G intron_variant ESAD-UK 15 50779326 50779326 single base substitution A G upstream_gene_variant ESAD-UK 15 50779912 50779912 single base substitution G T intron_variant ESAD-UK 15 50779912 50779912 single base substitution G T upstream_gene_variant ESAD-UK 15 50781520 50781520 single base substitution G A intron_variant ESAD-UK 15 50781520 50781520 single base substitution G A upstream_gene_variant ESAD-UK 15 50782342 50782342 single base substitution T A intron_variant ESAD-UK 15 50782342 50782342 single base substitution T A upstream_gene_variant ESAD-UK 15 50782713 50782713 single base substitution G A downstream_gene_variant ESAD-UK 15 50782713 50782713 single base substitution G A missense_variant R636Q 1907G>A ESAD-UK 15 50782713 50782713 single base substitution G A missense_variant R742Q 2225G>A ESAD-UK 15 50782713 50782713 single base substitution G A upstream_gene_variant ESAD-UK 15 50784654 50784654 single base substitution C T downstream_gene_variant ESAD-UK 15 50784654 50784654 single base substitution C T intron_variant ESAD-UK 15 50784654 50784654 single base substitution C T upstream_gene_variant ESAD-UK 15 50785770 50785770 single base substitution G A downstream_gene_variant ESAD-UK 15 50785770 50785770 single base substitution G A exon_variant ESAD-UK 15 50785770 50785770 single base substitution G A intron_variant ESAD-UK 15 50785770 50785770 single base substitution G A upstream_gene_variant ESAD-UK 15 50787394 50787394 deletion of <=200bp T - downstream_gene_variant ESAD-UK 15 50787394 50787394 deletion of <=200bp T - intron_variant ESAD-UK 15 50787394 50787394 deletion of <=200bp T - upstream_gene_variant ESAD-UK 15 50787430 50787430 insertion of <=200bp - TA downstream_gene_variant ESAD-UK 15 50787430 50787430 insertion of <=200bp - TA intron_variant ESAD-UK 15 50787430 50787430 insertion of <=200bp - TA upstream_gene_variant ESAD-UK 15 50789587 50789587 single base substitution T C intron_variant ESAD-UK 15 50789587 50789587 single base substitution T C upstream_gene_variant ESAD-UK 15 50789721 50789721 single base substitution T G intron_variant ESAD-UK 15 50789721 50789721 single base substitution T G upstream_gene_variant ESAD-UK 15 50795520 50795520 single base substitution C T downstream_gene_variant GBM-US 15 50788098 50788098 single base substitution T C exon_variant GBM-US 15 50788098 50788098 single base substitution T C synonymous_variant F798F 2394T>C GBM-US 15 50788098 50788098 single base substitution T C synonymous_variant F904F 2712T>C GBM-US 15 50788098 50788098 single base substitution T C upstream_gene_variant KIRC-US 15 50763851 50763851 single base substitution A G 3_prime_UTR_variant KIRC-US 15 50763851 50763851 single base substitution A G exon_variant KIRC-US 15 50763851 50763851 single base substitution A G intron_variant KIRC-US 15 50763851 50763851 single base substitution A G synonymous_variant E159E 477A>G KIRC-US 15 50763851 50763851 single base substitution A G synonymous_variant E236E 708A>G KIRC-US 15 50791105 50791105 single base substitution C G exon_variant KIRC-US 15 50791105 50791105 single base substitution C G missense_variant H1059Q 3177C>G KIRC-US 15 50791105 50791105 single base substitution C G missense_variant H953Q 2859C>G LAML-KR 15 50742281 50742281 single base substitution G A downstream_gene_variant LAML-KR 15 50742281 50742281 single base substitution G A intron_variant LAML-KR 15 50751050 50751050 single base substitution T C intron_variant LAML-KR 15 50751297 50751297 single base substitution G A 3_prime_UTR_variant LAML-KR 15 50751297 50751297 single base substitution G A downstream_gene_variant LAML-KR 15 50751297 50751297 single base substitution G A exon_variant LAML-KR 15 50751297 50751297 single base substitution G A intron_variant LAML-KR 15 50751297 50751297 single base substitution G A missense_variant G146S 436G>A LAML-KR 15 50751297 50751297 single base substitution G A missense_variant G69S 205G>A LAML-KR 15 50752194 50752194 single base substitution T C downstream_gene_variant LAML-KR 15 50752194 50752194 single base substitution T C intron_variant LAML-KR 15 50782836 50782836 single base substitution A C downstream_gene_variant LAML-KR 15 50782836 50782836 single base substitution A C intron_variant LAML-KR 15 50782836 50782836 single base substitution A C upstream_gene_variant LAML-KR 15 50784950 50784950 single base substitution C T downstream_gene_variant LAML-KR 15 50784950 50784950 single base substitution C T missense_variant R657W 1969C>T LAML-KR 15 50784950 50784950 single base substitution C T missense_variant R763W 2287C>T LAML-KR 15 50784950 50784950 single base substitution C T upstream_gene_variant LAML-KR 15 50784955 50784955 single base substitution C A downstream_gene_variant LAML-KR 15 50784955 50784955 single base substitution C A missense_variant N658K 1974C>A LAML-KR 15 50784955 50784955 single base substitution C A missense_variant N764K 2292C>A LAML-KR 15 50784955 50784955 single base substitution C A upstream_gene_variant LGG-US 15 50769066 50769066 single base substitution G C 3_prime_UTR_variant LGG-US 15 50769066 50769066 single base substitution G C exon_variant LGG-US 15 50769066 50769066 single base substitution G C intron_variant LGG-US 15 50769066 50769066 single base substitution G C synonymous_variant L213L 639G>C LGG-US 15 50769066 50769066 single base substitution G C synonymous_variant L290L 870G>C LICA-CN 15 50741656 50741656 single base substitution A T downstream_gene_variant LICA-CN 15 50741656 50741656 single base substitution A T exon_variant LICA-CN 15 50741656 50741656 single base substitution A T intron_variant LICA-CN 15 50741656 50741656 single base substitution A T missense_variant E103D 309A>T LICA-FR 15 50712360 50712360 deletion of <=200bp T - upstream_gene_variant LICA-FR 15 50712360 50712360 insertion of <=200bp - TT upstream_gene_variant LICA-FR 15 50716657 50716657 single base substitution G A 5_prime_UTR_variant LICA-FR 15 50716657 50716657 single base substitution G A exon_variant LICA-FR 15 50716657 50716657 single base substitution G A upstream_gene_variant LICA-FR 15 50720652 50720652 single base substitution A T intron_variant LICA-FR 15 50729831 50729831 single base substitution T A intron_variant LICA-FR 15 50729831 50729831 single base substitution T A upstream_gene_variant LICA-FR 15 50739346 50739346 single base substitution C T downstream_gene_variant LICA-FR 15 50739346 50739346 single base substitution C T intron_variant LICA-FR 15 50755300 50755300 single base substitution G A downstream_gene_variant LICA-FR 15 50755300 50755300 single base substitution G A intron_variant LICA-FR 15 50761831 50761831 single base substitution A G downstream_gene_variant LICA-FR 15 50761831 50761831 single base substitution A G intron_variant LICA-FR 15 50766205 50766205 single base substitution T C downstream_gene_variant LICA-FR 15 50766205 50766205 single base substitution T C intron_variant LICA-FR 15 50786350 50786350 single base substitution A G downstream_gene_variant LICA-FR 15 50786350 50786350 single base substitution A G exon_variant LICA-FR 15 50786350 50786350 single base substitution A G missense_variant Y738C 2213A>G LICA-FR 15 50786350 50786350 single base substitution A G missense_variant Y844C 2531A>G LICA-FR 15 50786350 50786350 single base substitution A G upstream_gene_variant LICA-FR 15 50787215 50787215 deletion of <=200bp A - downstream_gene_variant LICA-FR 15 50787215 50787215 deletion of <=200bp A - intron_variant LICA-FR 15 50787215 50787215 deletion of <=200bp A - upstream_gene_variant LICA-FR 15 50793033 50793033 deletion of <=200bp T - 3_prime_UTR_variant LICA-FR 15 50793033 50793033 deletion of <=200bp T - downstream_gene_variant LIHC-US 15 50782610 50782610 single base substitution A G exon_variant LIHC-US 15 50782610 50782610 single base substitution A G missense_variant R602G 1804A>G LIHC-US 15 50782610 50782610 single base substitution A G missense_variant R708G 2122A>G LIHC-US 15 50782610 50782610 single base substitution A G upstream_gene_variant LINC-JP 15 50715600 50715600 single base substitution T G upstream_gene_variant LINC-JP 15 50715613 50715613 single base substitution T C upstream_gene_variant LINC-JP 15 50729182 50729182 deletion of <=200bp T - intron_variant LINC-JP 15 50729182 50729182 deletion of <=200bp T - upstream_gene_variant LINC-JP 15 50731132 50731132 deletion of <=200bp T - intron_variant LINC-JP 15 50731132 50731132 deletion of <=200bp T - upstream_gene_variant LINC-JP 15 50737594 50737594 single base substitution T C downstream_gene_variant LINC-JP 15 50737594 50737594 single base substitution T C intron_variant LINC-JP 15 50743282 50743282 single base substitution C T downstream_gene_variant LINC-JP 15 50743282 50743282 single base substitution C T intron_variant LINC-JP 15 50761759 50761759 single base substitution T G downstream_gene_variant LINC-JP 15 50761759 50761759 single base substitution T G intron_variant LINC-JP 15 50762656 50762656 single base substitution G T intron_variant LINC-JP 15 50772831 50772831 deletion of <=200bp T - intron_variant LINC-JP 15 50776221 50776221 single base substitution A T downstream_gene_variant LINC-JP 15 50776221 50776221 single base substitution A T intron_variant LINC-JP 15 50777108 50777108 single base substitution T G downstream_gene_variant LINC-JP 15 50777108 50777108 single base substitution T G intron_variant LINC-JP 15 50777108 50777108 single base substitution T G upstream_gene_variant LINC-JP 15 50783916 50783916 single base substitution A G downstream_gene_variant LINC-JP 15 50783916 50783916 single base substitution A G intron_variant LINC-JP 15 50783916 50783916 single base substitution A G upstream_gene_variant LINC-JP 15 50785371 50785371 single base substitution A C downstream_gene_variant LINC-JP 15 50785371 50785371 single base substitution A C intron_variant LINC-JP 15 50785371 50785371 single base substitution A C upstream_gene_variant LINC-JP 15 50785793 50785793 single base substitution T A downstream_gene_variant LINC-JP 15 50785793 50785793 single base substitution T A exon_variant LINC-JP 15 50785793 50785793 single base substitution T A intron_variant LINC-JP 15 50785793 50785793 single base substitution T A upstream_gene_variant LINC-JP 15 50790976 50790976 single base substitution A G intron_variant LIRI-JP 15 50717703 50717703 single base substitution T A intron_variant LIRI-JP 15 50717703 50717703 single base substitution T A upstream_gene_variant LIRI-JP 15 50718130 50718130 single base substitution C A intron_variant LIRI-JP 15 50718130 50718130 single base substitution C A upstream_gene_variant LIRI-JP 15 50718146 50718146 single base substitution C A intron_variant LIRI-JP 15 50718146 50718146 single base substitution C A upstream_gene_variant LIRI-JP 15 50720293 50720293 single base substitution A C intron_variant LIRI-JP 15 50720294 50720294 single base substitution C T intron_variant LIRI-JP 15 50721390 50721390 single base substitution T A intron_variant LIRI-JP 15 50723059 50723059 single base substitution G A intron_variant LIRI-JP 15 50727552 50727552 single base substitution T C intron_variant LIRI-JP 15 50727552 50727552 single base substitution T C upstream_gene_variant LIRI-JP 15 50727696 50727696 single base substitution T G intron_variant LIRI-JP 15 50727696 50727696 single base substitution T G upstream_gene_variant LIRI-JP 15 50728118 50728118 single base substitution T C intron_variant LIRI-JP 15 50728118 50728118 single base substitution T C upstream_gene_variant LIRI-JP 15 50728232 50728232 single base substitution T C intron_variant LIRI-JP 15 50728232 50728232 single base substitution T C upstream_gene_variant LIRI-JP 15 50728807 50728807 single base substitution A T intron_variant LIRI-JP 15 50728807 50728807 single base substitution A T upstream_gene_variant LIRI-JP 15 50735749 50735749 single base substitution C T downstream_gene_variant LIRI-JP 15 50735749 50735749 single base substitution C T intron_variant LIRI-JP 15 50736629 50736629 single base substitution A G downstream_gene_variant LIRI-JP 15 50736629 50736629 single base substitution A G intron_variant LIRI-JP 15 50736902 50736902 single base substitution A G downstream_gene_variant LIRI-JP 15 50736902 50736902 single base substitution A G intron_variant LIRI-JP 15 50737033 50737033 single base substitution C G downstream_gene_variant LIRI-JP 15 50737033 50737033 single base substitution C G intron_variant LIRI-JP 15 50737351 50737351 single base substitution T C downstream_gene_variant LIRI-JP 15 50737351 50737351 single base substitution T C intron_variant LIRI-JP 15 50738725 50738725 single base substitution A G downstream_gene_variant LIRI-JP 15 50738725 50738725 single base substitution A G intron_variant LIRI-JP 15 50740528 50740528 single base substitution A G downstream_gene_variant LIRI-JP 15 50740528 50740528 single base substitution A G intron_variant LIRI-JP 15 50742576 50742576 single base substitution A G downstream_gene_variant LIRI-JP 15 50742576 50742576 single base substitution A G intron_variant LIRI-JP 15 50745325 50745325 single base substitution C T downstream_gene_variant LIRI-JP 15 50745325 50745325 single base substitution C T intron_variant LIRI-JP 15 50745555 50745555 single base substitution A G downstream_gene_variant LIRI-JP 15 50745555 50745555 single base substitution A G intron_variant LIRI-JP 15 50746251 50746251 single base substitution G A downstream_gene_variant LIRI-JP 15 50746251 50746251 single base substitution G A intron_variant LIRI-JP 15 50746251 50746251 single base substitution G A upstream_gene_variant LIRI-JP 15 50746262 50746262 single base substitution T A downstream_gene_variant LIRI-JP 15 50746262 50746262 single base substitution T A intron_variant LIRI-JP 15 50746262 50746262 single base substitution T A upstream_gene_variant LIRI-JP 15 50747857 50747857 single base substitution A G intron_variant LIRI-JP 15 50747857 50747857 single base substitution A G upstream_gene_variant LIRI-JP 15 50752086 50752086 single base substitution T C downstream_gene_variant LIRI-JP 15 50752086 50752086 single base substitution T C intron_variant LIRI-JP 15 50757008 50757008 single base substitution G T downstream_gene_variant LIRI-JP 15 50757008 50757008 single base substitution G T intron_variant LIRI-JP 15 50758144 50758144 single base substitution A G downstream_gene_variant LIRI-JP 15 50758144 50758144 single base substitution A G intron_variant LIRI-JP 15 50758497 50758497 single base substitution A C downstream_gene_variant LIRI-JP 15 50758497 50758497 single base substitution A C intron_variant LIRI-JP 15 50762141 50762141 single base substitution G A downstream_gene_variant LIRI-JP 15 50762141 50762141 single base substitution G A intron_variant LIRI-JP 15 50763815 50763815 single base substitution A G intron_variant LIRI-JP 15 50767393 50767393 single base substitution C G downstream_gene_variant LIRI-JP 15 50767393 50767393 single base substitution C G intron_variant LIRI-JP 15 50769038 50769038 single base substitution A G intron_variant LIRI-JP 15 50769038 50769038 single base substitution A G splice_region_variant LIRI-JP 15 50770349 50770349 single base substitution T G intron_variant LIRI-JP 15 50770949 50770949 single base substitution C T intron_variant LIRI-JP 15 50772535 50772535 single base substitution T C intron_variant LIRI-JP 15 50775347 50775347 single base substitution A G downstream_gene_variant LIRI-JP 15 50775347 50775347 single base substitution A G intron_variant LIRI-JP 15 50776929 50776929 single base substitution A C downstream_gene_variant LIRI-JP 15 50776929 50776929 single base substitution A C intron_variant LIRI-JP 15 50776929 50776929 single base substitution A C upstream_gene_variant LIRI-JP 15 50777567 50777567 single base substitution A G downstream_gene_variant LIRI-JP 15 50777567 50777567 single base substitution A G intron_variant LIRI-JP 15 50777567 50777567 single base substitution A G upstream_gene_variant LIRI-JP 15 50778299 50778299 single base substitution T A downstream_gene_variant LIRI-JP 15 50778299 50778299 single base substitution T A intron_variant LIRI-JP 15 50778299 50778299 single base substitution T A upstream_gene_variant LIRI-JP 15 50781050 50781050 single base substitution G A intron_variant LIRI-JP 15 50781050 50781050 single base substitution G A upstream_gene_variant LIRI-JP 15 50781366 50781366 single base substitution T G intron_variant LIRI-JP 15 50781366 50781366 single base substitution T G upstream_gene_variant LIRI-JP 15 50781515 50781515 single base substitution A G intron_variant LIRI-JP 15 50781515 50781515 single base substitution A G upstream_gene_variant LIRI-JP 15 50783172 50783172 single base substitution A G downstream_gene_variant LIRI-JP 15 50783172 50783172 single base substitution A G intron_variant LIRI-JP 15 50783172 50783172 single base substitution A G upstream_gene_variant LIRI-JP 15 50783174 50783174 single base substitution A G downstream_gene_variant LIRI-JP 15 50783174 50783174 single base substitution A G intron_variant LIRI-JP 15 50783174 50783174 single base substitution A G upstream_gene_variant LIRI-JP 15 50783294 50783294 single base substitution T G downstream_gene_variant LIRI-JP 15 50783294 50783294 single base substitution T G intron_variant LIRI-JP 15 50783294 50783294 single base substitution T G upstream_gene_variant LIRI-JP 15 50783597 50783597 single base substitution A G downstream_gene_variant LIRI-JP 15 50783597 50783597 single base substitution A G intron_variant LIRI-JP 15 50783597 50783597 single base substitution A G upstream_gene_variant LIRI-JP 15 50791761 50791761 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 50791761 50791761 single base substitution T G downstream_gene_variant LIRI-JP 15 50791761 50791761 single base substitution T G exon_variant LIRI-JP 15 50793356 50793373 deletion of <=200bp ACAATAAGAAGATAATTC - downstream_gene_variant LIRI-JP 15 50793734 50793734 single base substitution A G downstream_gene_variant LIRI-JP 15 50794072 50794072 single base substitution A G downstream_gene_variant LIRI-JP 15 50797804 50797804 single base substitution A G downstream_gene_variant LUSC-KR 15 50711720 50711720 single base substitution G T upstream_gene_variant LUSC-KR 15 50722292 50722292 single base substitution G T intron_variant LUSC-KR 15 50735512 50735512 single base substitution A T downstream_gene_variant LUSC-KR 15 50735512 50735512 single base substitution A T intron_variant LUSC-KR 15 50735753 50735753 single base substitution T A downstream_gene_variant LUSC-KR 15 50735753 50735753 single base substitution T A intron_variant LUSC-KR 15 50737734 50737734 single base substitution G C downstream_gene_variant LUSC-KR 15 50737734 50737734 single base substitution G C intron_variant LUSC-KR 15 50744624 50744624 single base substitution G A downstream_gene_variant LUSC-KR 15 50744624 50744624 single base substitution G A intron_variant LUSC-KR 15 50746080 50746080 single base substitution G T downstream_gene_variant LUSC-KR 15 50746080 50746080 single base substitution G T intron_variant LUSC-KR 15 50746080 50746080 single base substitution G T upstream_gene_variant LUSC-KR 15 50751931 50751931 single base substitution G T downstream_gene_variant LUSC-KR 15 50751931 50751931 single base substitution G T intron_variant LUSC-KR 15 50753742 50753742 single base substitution G C downstream_gene_variant LUSC-KR 15 50753742 50753742 single base substitution G C intron_variant LUSC-KR 15 50758577 50758577 single base substitution C T downstream_gene_variant LUSC-KR 15 50758577 50758577 single base substitution C T intron_variant LUSC-KR 15 50767723 50767723 single base substitution A G downstream_gene_variant LUSC-KR 15 50767723 50767723 single base substitution A G intron_variant LUSC-KR 15 50776962 50776962 single base substitution T G downstream_gene_variant LUSC-KR 15 50776962 50776962 single base substitution T G intron_variant LUSC-KR 15 50776962 50776962 single base substitution T G upstream_gene_variant LUSC-KR 15 50782446 50782446 single base substitution C T intron_variant LUSC-KR 15 50782446 50782446 single base substitution C T upstream_gene_variant LUSC-KR 15 50784950 50784950 single base substitution C T downstream_gene_variant LUSC-KR 15 50784950 50784950 single base substitution C T missense_variant R657W 1969C>T LUSC-KR 15 50784950 50784950 single base substitution C T missense_variant R763W 2287C>T LUSC-KR 15 50784950 50784950 single base substitution C T upstream_gene_variant LUSC-KR 15 50784955 50784955 single base substitution C A downstream_gene_variant LUSC-KR 15 50784955 50784955 single base substitution C A missense_variant N658K 1974C>A LUSC-KR 15 50784955 50784955 single base substitution C A missense_variant N764K 2292C>A LUSC-KR 15 50784955 50784955 single base substitution C A upstream_gene_variant LUSC-US 15 50733609 50733609 single base substitution G A exon_variant LUSC-US 15 50733609 50733609 single base substitution G A intron_variant LUSC-US 15 50733609 50733609 single base substitution G A synonymous_variant E56E 168G>A LUSC-US 15 50757333 50757333 single base substitution C G 3_prime_UTR_variant LUSC-US 15 50757333 50757333 single base substitution C G downstream_gene_variant LUSC-US 15 50757333 50757333 single base substitution C G exon_variant LUSC-US 15 50757333 50757333 single base substitution C G intron_variant LUSC-US 15 50757333 50757333 single base substitution C G missense_variant Q134E 400C>G LUSC-US 15 50757333 50757333 single base substitution C G missense_variant Q211E 631C>G LUSC-US 15 50769081 50769081 single base substitution G T 3_prime_UTR_variant LUSC-US 15 50769081 50769081 single base substitution G T exon_variant LUSC-US 15 50769081 50769081 single base substitution G T intron_variant LUSC-US 15 50769081 50769081 single base substitution G T missense_variant L218F 654G>T LUSC-US 15 50769081 50769081 single base substitution G T missense_variant L295F 885G>T LUSC-US 15 50769124 50769124 single base substitution C T 3_prime_UTR_variant LUSC-US 15 50769124 50769124 single base substitution C T exon_variant LUSC-US 15 50769124 50769124 single base substitution C T intron_variant LUSC-US 15 50769124 50769124 single base substitution C T stop_gained Q233* 697C>T LUSC-US 15 50769124 50769124 single base substitution C T stop_gained Q310* 928C>T LUSC-US 15 50786304 50786304 single base substitution G C downstream_gene_variant LUSC-US 15 50786304 50786304 single base substitution G C exon_variant LUSC-US 15 50786304 50786304 single base substitution G C missense_variant E723Q 2167G>C LUSC-US 15 50786304 50786304 single base substitution G C missense_variant E829Q 2485G>C LUSC-US 15 50786304 50786304 single base substitution G C upstream_gene_variant MALY-DE 15 50711713 50711713 single base substitution A G upstream_gene_variant MALY-DE 15 50715431 50715431 single base substitution C A upstream_gene_variant MALY-DE 15 50727479 50727479 single base substitution A T intron_variant MALY-DE 15 50727479 50727479 single base substitution A T upstream_gene_variant MALY-DE 15 50728540 50728540 single base substitution A T intron_variant MALY-DE 15 50728540 50728540 single base substitution A T upstream_gene_variant MALY-DE 15 50731391 50731391 single base substitution G A intron_variant MALY-DE 15 50733475 50733475 single base substitution A T intron_variant MALY-DE 15 50735674 50735674 single base substitution G T downstream_gene_variant MALY-DE 15 50735674 50735674 single base substitution G T intron_variant MALY-DE 15 50736988 50736988 single base substitution C G downstream_gene_variant MALY-DE 15 50736988 50736988 single base substitution C G intron_variant MALY-DE 15 50740731 50740731 single base substitution T G downstream_gene_variant MALY-DE 15 50740731 50740731 single base substitution T G intron_variant MALY-DE 15 50745355 50745355 insertion of <=200bp - A downstream_gene_variant MALY-DE 15 50745355 50745355 insertion of <=200bp - A intron_variant MALY-DE 15 50761942 50761942 single base substitution T A downstream_gene_variant MALY-DE 15 50761942 50761942 single base substitution T A intron_variant MALY-DE 15 50770937 50770937 single base substitution T G intron_variant MALY-DE 15 50780537 50780537 single base substitution T G intron_variant MALY-DE 15 50780537 50780537 single base substitution T G upstream_gene_variant MALY-DE 15 50780556 50780556 single base substitution T C intron_variant MALY-DE 15 50780556 50780556 single base substitution T C upstream_gene_variant MALY-DE 15 50782497 50782497 single base substitution A G exon_variant MALY-DE 15 50782497 50782497 single base substitution A G missense_variant H564R 1691A>G MALY-DE 15 50782497 50782497 single base substitution A G missense_variant H670R 2009A>G MALY-DE 15 50782497 50782497 single base substitution A G upstream_gene_variant MALY-DE 15 50782653 50782653 single base substitution T A downstream_gene_variant MALY-DE 15 50782653 50782653 single base substitution T A missense_variant I616K 1847T>A MALY-DE 15 50782653 50782653 single base substitution T A missense_variant I722K 2165T>A MALY-DE 15 50782653 50782653 single base substitution T A upstream_gene_variant MALY-DE 15 50782669 50782669 single base substitution A G downstream_gene_variant MALY-DE 15 50782669 50782669 single base substitution A G synonymous_variant Q621Q 1863A>G MALY-DE 15 50782669 50782669 single base substitution A G synonymous_variant Q727Q 2181A>G MALY-DE 15 50782669 50782669 single base substitution A G upstream_gene_variant MALY-DE 15 50782695 50782695 single base substitution T C downstream_gene_variant MALY-DE 15 50782695 50782695 single base substitution T C missense_variant V630A 1889T>C MALY-DE 15 50782695 50782695 single base substitution T C missense_variant V736A 2207T>C MALY-DE 15 50782695 50782695 single base substitution T C upstream_gene_variant MALY-DE 15 50785029 50785029 single base substitution A G downstream_gene_variant MALY-DE 15 50785029 50785029 single base substitution A G missense_variant N683S 2048A>G MALY-DE 15 50785029 50785029 single base substitution A G missense_variant N789S 2366A>G MALY-DE 15 50785029 50785029 single base substitution A G upstream_gene_variant MALY-DE 15 50787387 50787388 deletion of <=200bp AT - downstream_gene_variant MALY-DE 15 50787387 50787388 deletion of <=200bp AT - intron_variant MALY-DE 15 50787387 50787388 deletion of <=200bp AT - upstream_gene_variant MELA-AU 15 50712025 50712025 single base substitution C T upstream_gene_variant MELA-AU 15 50712113 50712113 single base substitution G A upstream_gene_variant MELA-AU 15 50712670 50712670 single base substitution G A upstream_gene_variant MELA-AU 15 50713152 50713152 single base substitution G A upstream_gene_variant MELA-AU 15 50713443 50713443 single base substitution A G upstream_gene_variant MELA-AU 15 50713447 50713447 single base substitution C T upstream_gene_variant MELA-AU 15 50713872 50713872 single base substitution C T upstream_gene_variant MELA-AU 15 50714138 50714138 single base substitution A G upstream_gene_variant MELA-AU 15 50714488 50714488 single base substitution C T upstream_gene_variant MELA-AU 15 50716015 50716015 single base substitution C T upstream_gene_variant MELA-AU 15 50716397 50716397 single base substitution G A upstream_gene_variant MELA-AU 15 50716519 50716519 single base substitution G A upstream_gene_variant MELA-AU 15 50716556 50716556 single base substitution G A upstream_gene_variant MELA-AU 15 50716557 50716557 single base substitution G A upstream_gene_variant MELA-AU 15 50716892 50716892 single base substitution C T intron_variant MELA-AU 15 50716892 50716892 single base substitution C T upstream_gene_variant MELA-AU 15 50717602 50717602 single base substitution T A intron_variant MELA-AU 15 50717602 50717602 single base substitution T A upstream_gene_variant MELA-AU 15 50717911 50717911 single base substitution T A intron_variant MELA-AU 15 50717911 50717911 single base substitution T A upstream_gene_variant MELA-AU 15 50718460 50718460 single base substitution G A intron_variant MELA-AU 15 50718460 50718460 single base substitution G A upstream_gene_variant MELA-AU 15 50721616 50721616 single base substitution C T intron_variant MELA-AU 15 50721981 50721981 single base substitution T A intron_variant MELA-AU 15 50722441 50722442 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 50722503 50722503 single base substitution C T intron_variant MELA-AU 15 50722883 50722883 single base substitution G A intron_variant MELA-AU 15 50723701 50723701 single base substitution C T intron_variant MELA-AU 15 50723883 50723883 single base substitution C T intron_variant MELA-AU 15 50724037 50724037 single base substitution G A intron_variant MELA-AU 15 50724154 50724154 single base substitution G A intron_variant MELA-AU 15 50724248 50724248 single base substitution G A intron_variant MELA-AU 15 50725446 50725446 single base substitution T G intron_variant MELA-AU 15 50725629 50725629 single base substitution G A intron_variant MELA-AU 15 50725806 50725806 single base substitution T C intron_variant MELA-AU 15 50725808 50725808 single base substitution T C intron_variant MELA-AU 15 50726407 50726407 single base substitution T A intron_variant MELA-AU 15 50726407 50726407 single base substitution T A upstream_gene_variant MELA-AU 15 50726450 50726450 single base substitution C A intron_variant MELA-AU 15 50726450 50726450 single base substitution C A upstream_gene_variant MELA-AU 15 50727569 50727569 single base substitution A G intron_variant MELA-AU 15 50727569 50727569 single base substitution A G upstream_gene_variant MELA-AU 15 50728029 50728029 single base substitution C T intron_variant MELA-AU 15 50728029 50728029 single base substitution C T upstream_gene_variant MELA-AU 15 50728376 50728376 single base substitution C T intron_variant MELA-AU 15 50728376 50728376 single base substitution C T upstream_gene_variant MELA-AU 15 50728989 50728989 single base substitution C T intron_variant MELA-AU 15 50728989 50728989 single base substitution C T upstream_gene_variant MELA-AU 15 50729244 50729244 single base substitution C T intron_variant MELA-AU 15 50729244 50729244 single base substitution C T upstream_gene_variant MELA-AU 15 50729279 50729279 single base substitution C T intron_variant MELA-AU 15 50729279 50729279 single base substitution C T upstream_gene_variant MELA-AU 15 50730288 50730288 single base substitution T C intron_variant MELA-AU 15 50730288 50730288 single base substitution T C upstream_gene_variant MELA-AU 15 50731526 50731526 single base substitution C T intron_variant MELA-AU 15 50731807 50731807 single base substitution G A intron_variant MELA-AU 15 50732027 50732028 multiple base substitution (>=2bp and <=200bp) TT AA intron_variant MELA-AU 15 50732106 50732106 single base substitution G A intron_variant MELA-AU 15 50732200 50732200 single base substitution C T intron_variant MELA-AU 15 50732293 50732293 single base substitution G A intron_variant MELA-AU 15 50733122 50733122 single base substitution C T intron_variant MELA-AU 15 50734307 50734307 single base substitution G A downstream_gene_variant MELA-AU 15 50734307 50734307 single base substitution G A intron_variant MELA-AU 15 50734444 50734444 single base substitution T G downstream_gene_variant MELA-AU 15 50734444 50734444 single base substitution T G intron_variant MELA-AU 15 50734493 50734493 single base substitution C T downstream_gene_variant MELA-AU 15 50734493 50734493 single base substitution C T intron_variant MELA-AU 15 50734609 50734609 single base substitution G C downstream_gene_variant MELA-AU 15 50734609 50734609 single base substitution G C intron_variant MELA-AU 15 50735208 50735208 single base substitution C T downstream_gene_variant MELA-AU 15 50735208 50735208 single base substitution C T intron_variant MELA-AU 15 50735346 50735346 single base substitution C T downstream_gene_variant MELA-AU 15 50735346 50735346 single base substitution C T intron_variant MELA-AU 15 50735447 50735447 single base substitution C T downstream_gene_variant MELA-AU 15 50735447 50735447 single base substitution C T intron_variant MELA-AU 15 50735575 50735575 single base substitution T C downstream_gene_variant MELA-AU 15 50735575 50735575 single base substitution T C intron_variant MELA-AU 15 50735666 50735666 single base substitution G A downstream_gene_variant MELA-AU 15 50735666 50735666 single base substitution G A intron_variant MELA-AU 15 50735804 50735804 single base substitution C T downstream_gene_variant MELA-AU 15 50735804 50735804 single base substitution C T intron_variant MELA-AU 15 50736134 50736134 single base substitution C T downstream_gene_variant MELA-AU 15 50736134 50736134 single base substitution C T intron_variant MELA-AU 15 50737288 50737288 single base substitution C T downstream_gene_variant MELA-AU 15 50737288 50737288 single base substitution C T intron_variant MELA-AU 15 50737302 50737302 single base substitution C T downstream_gene_variant MELA-AU 15 50737302 50737302 single base substitution C T intron_variant MELA-AU 15 50739882 50739882 single base substitution C T downstream_gene_variant MELA-AU 15 50739882 50739882 single base substitution C T intron_variant MELA-AU 15 50740025 50740025 single base substitution C T downstream_gene_variant MELA-AU 15 50740025 50740025 single base substitution C T intron_variant MELA-AU 15 50740189 50740189 single base substitution C T downstream_gene_variant MELA-AU 15 50740189 50740189 single base substitution C T intron_variant MELA-AU 15 50740975 50740975 single base substitution C T downstream_gene_variant MELA-AU 15 50740975 50740975 single base substitution C T intron_variant MELA-AU 15 50742131 50742132 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 50742131 50742132 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 50742548 50742548 single base substitution A T downstream_gene_variant MELA-AU 15 50742548 50742548 single base substitution A T intron_variant MELA-AU 15 50742999 50742999 single base substitution C T downstream_gene_variant MELA-AU 15 50742999 50742999 single base substitution C T intron_variant MELA-AU 15 50743303 50743303 single base substitution C T downstream_gene_variant MELA-AU 15 50743303 50743303 single base substitution C T intron_variant MELA-AU 15 50743815 50743815 single base substitution G A downstream_gene_variant MELA-AU 15 50743815 50743815 single base substitution G A intron_variant MELA-AU 15 50743980 50743980 single base substitution C T downstream_gene_variant MELA-AU 15 50743980 50743980 single base substitution C T intron_variant MELA-AU 15 50744912 50744912 single base substitution C T downstream_gene_variant MELA-AU 15 50744912 50744912 single base substitution C T intron_variant MELA-AU 15 50745049 50745049 single base substitution C T downstream_gene_variant MELA-AU 15 50745049 50745049 single base substitution C T intron_variant MELA-AU 15 50745847 50745847 single base substitution C T downstream_gene_variant MELA-AU 15 50745847 50745847 single base substitution C T intron_variant MELA-AU 15 50745847 50745847 single base substitution C T upstream_gene_variant MELA-AU 15 50746425 50746425 single base substitution C T downstream_gene_variant MELA-AU 15 50746425 50746425 single base substitution C T intron_variant MELA-AU 15 50746425 50746425 single base substitution C T upstream_gene_variant MELA-AU 15 50746426 50746426 single base substitution C T downstream_gene_variant MELA-AU 15 50746426 50746426 single base substitution C T intron_variant MELA-AU 15 50746426 50746426 single base substitution C T upstream_gene_variant MELA-AU 15 50746835 50746835 single base substitution A G intron_variant MELA-AU 15 50746835 50746835 single base substitution A G upstream_gene_variant MELA-AU 15 50746983 50746983 single base substitution C T intron_variant MELA-AU 15 50746983 50746983 single base substitution C T upstream_gene_variant MELA-AU 15 50747133 50747133 single base substitution C T intron_variant MELA-AU 15 50747133 50747133 single base substitution C T upstream_gene_variant MELA-AU 15 50747283 50747283 single base substitution C T intron_variant MELA-AU 15 50747283 50747283 single base substitution C T upstream_gene_variant MELA-AU 15 50747284 50747284 deletion of <=200bp T - intron_variant MELA-AU 15 50747284 50747284 deletion of <=200bp T - upstream_gene_variant MELA-AU 15 50747691 50747691 single base substitution T C intron_variant MELA-AU 15 50747691 50747691 single base substitution T C upstream_gene_variant MELA-AU 15 50748361 50748361 single base substitution G A intron_variant MELA-AU 15 50748361 50748361 single base substitution G A upstream_gene_variant MELA-AU 15 50749149 50749149 single base substitution C T intron_variant MELA-AU 15 50749149 50749149 single base substitution C T upstream_gene_variant MELA-AU 15 50749168 50749168 single base substitution G A intron_variant MELA-AU 15 50749168 50749168 single base substitution G A upstream_gene_variant MELA-AU 15 50749289 50749289 single base substitution G T intron_variant MELA-AU 15 50749289 50749289 single base substitution G T upstream_gene_variant MELA-AU 15 50749552 50749552 single base substitution C T intron_variant MELA-AU 15 50749552 50749552 single base substitution C T upstream_gene_variant MELA-AU 15 50750006 50750006 single base substitution C T intron_variant MELA-AU 15 50750006 50750006 single base substitution C T upstream_gene_variant MELA-AU 15 50750395 50750395 single base substitution C T intron_variant MELA-AU 15 50750395 50750395 single base substitution C T upstream_gene_variant MELA-AU 15 50750664 50750664 single base substitution G A intron_variant MELA-AU 15 50750664 50750664 single base substitution G A upstream_gene_variant MELA-AU 15 50750828 50750828 single base substitution C T intron_variant MELA-AU 15 50751046 50751046 single base substitution C T intron_variant MELA-AU 15 50751424 50751424 single base substitution G A downstream_gene_variant MELA-AU 15 50751424 50751424 single base substitution G A intron_variant MELA-AU 15 50751840 50751840 single base substitution C T downstream_gene_variant MELA-AU 15 50751840 50751840 single base substitution C T intron_variant MELA-AU 15 50752188 50752188 single base substitution C G downstream_gene_variant MELA-AU 15 50752188 50752188 single base substitution C G intron_variant MELA-AU 15 50752951 50752951 single base substitution C T downstream_gene_variant MELA-AU 15 50752951 50752951 single base substitution C T intron_variant MELA-AU 15 50752971 50752971 single base substitution C T downstream_gene_variant MELA-AU 15 50752971 50752971 single base substitution C T intron_variant MELA-AU 15 50753119 50753119 single base substitution C T downstream_gene_variant MELA-AU 15 50753119 50753119 single base substitution C T intron_variant MELA-AU 15 50753219 50753219 single base substitution C T downstream_gene_variant MELA-AU 15 50753219 50753219 single base substitution C T intron_variant MELA-AU 15 50753323 50753323 single base substitution G A downstream_gene_variant MELA-AU 15 50753323 50753323 single base substitution G A intron_variant MELA-AU 15 50753368 50753368 single base substitution T G downstream_gene_variant MELA-AU 15 50753368 50753368 single base substitution T G intron_variant MELA-AU 15 50753584 50753584 single base substitution C T downstream_gene_variant MELA-AU 15 50753584 50753584 single base substitution C T intron_variant MELA-AU 15 50754111 50754111 single base substitution T A downstream_gene_variant MELA-AU 15 50754111 50754111 single base substitution T A intron_variant MELA-AU 15 50754127 50754127 single base substitution A T downstream_gene_variant MELA-AU 15 50754127 50754127 single base substitution A T intron_variant MELA-AU 15 50754386 50754386 single base substitution G A downstream_gene_variant MELA-AU 15 50754386 50754386 single base substitution G A intron_variant MELA-AU 15 50754393 50754393 single base substitution C T downstream_gene_variant MELA-AU 15 50754393 50754393 single base substitution C T intron_variant MELA-AU 15 50754735 50754735 single base substitution C T downstream_gene_variant MELA-AU 15 50754735 50754735 single base substitution C T intron_variant MELA-AU 15 50755091 50755091 single base substitution C T downstream_gene_variant MELA-AU 15 50755091 50755091 single base substitution C T intron_variant MELA-AU 15 50755160 50755160 single base substitution C T downstream_gene_variant MELA-AU 15 50755160 50755160 single base substitution C T intron_variant MELA-AU 15 50755211 50755211 single base substitution C T downstream_gene_variant MELA-AU 15 50755211 50755211 single base substitution C T intron_variant MELA-AU 15 50755252 50755252 single base substitution C T downstream_gene_variant MELA-AU 15 50755252 50755252 single base substitution C T intron_variant MELA-AU 15 50755265 50755265 single base substitution T C downstream_gene_variant MELA-AU 15 50755265 50755265 single base substitution T C intron_variant MELA-AU 15 50755433 50755433 single base substitution C T downstream_gene_variant MELA-AU 15 50755433 50755433 single base substitution C T intron_variant MELA-AU 15 50755546 50755546 single base substitution G A downstream_gene_variant MELA-AU 15 50755546 50755546 single base substitution G A intron_variant MELA-AU 15 50755907 50755907 single base substitution G A downstream_gene_variant MELA-AU 15 50755907 50755907 single base substitution G A intron_variant MELA-AU 15 50756574 50756574 single base substitution C T downstream_gene_variant MELA-AU 15 50756574 50756574 single base substitution C T intron_variant MELA-AU 15 50756809 50756809 single base substitution T C downstream_gene_variant MELA-AU 15 50756809 50756809 single base substitution T C intron_variant MELA-AU 15 50756983 50756983 single base substitution G C downstream_gene_variant MELA-AU 15 50756983 50756983 single base substitution G C intron_variant MELA-AU 15 50757275 50757275 single base substitution G A 3_prime_UTR_variant MELA-AU 15 50757275 50757275 single base substitution G A downstream_gene_variant MELA-AU 15 50757275 50757275 single base substitution G A exon_variant MELA-AU 15 50757275 50757275 single base substitution G A intron_variant MELA-AU 15 50757275 50757275 single base substitution G A missense_variant M114I 342G>A MELA-AU 15 50757275 50757275 single base substitution G A missense_variant M191I 573G>A MELA-AU 15 50758517 50758517 single base substitution C T downstream_gene_variant MELA-AU 15 50758517 50758517 single base substitution C T intron_variant MELA-AU 15 50759140 50759140 single base substitution T A downstream_gene_variant MELA-AU 15 50759140 50759140 single base substitution T A intron_variant MELA-AU 15 50759157 50759157 single base substitution C T downstream_gene_variant MELA-AU 15 50759157 50759157 single base substitution C T intron_variant MELA-AU 15 50760170 50760170 single base substitution C T downstream_gene_variant MELA-AU 15 50760170 50760170 single base substitution C T intron_variant MELA-AU 15 50760889 50760889 single base substitution C T downstream_gene_variant MELA-AU 15 50760889 50760889 single base substitution C T intron_variant MELA-AU 15 50761129 50761129 single base substitution C T downstream_gene_variant MELA-AU 15 50761129 50761129 single base substitution C T intron_variant MELA-AU 15 50761663 50761663 single base substitution T C downstream_gene_variant MELA-AU 15 50761663 50761663 single base substitution T C intron_variant MELA-AU 15 50761703 50761703 single base substitution C T downstream_gene_variant MELA-AU 15 50761703 50761703 single base substitution C T intron_variant MELA-AU 15 50761725 50761725 single base substitution C T downstream_gene_variant MELA-AU 15 50761725 50761725 single base substitution C T intron_variant MELA-AU 15 50761801 50761801 single base substitution A G downstream_gene_variant MELA-AU 15 50761801 50761801 single base substitution A G intron_variant MELA-AU 15 50762026 50762026 single base substitution C T downstream_gene_variant MELA-AU 15 50762026 50762026 single base substitution C T intron_variant MELA-AU 15 50764094 50764094 single base substitution C T downstream_gene_variant MELA-AU 15 50764094 50764094 single base substitution C T intron_variant MELA-AU 15 50764282 50764282 single base substitution G A downstream_gene_variant MELA-AU 15 50764282 50764282 single base substitution G A intron_variant MELA-AU 15 50764617 50764618 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 50764617 50764618 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 50765026 50765026 single base substitution G A downstream_gene_variant MELA-AU 15 50765026 50765026 single base substitution G A intron_variant MELA-AU 15 50765096 50765096 single base substitution G A downstream_gene_variant MELA-AU 15 50765096 50765096 single base substitution G A intron_variant MELA-AU 15 50766040 50766040 single base substitution T G downstream_gene_variant MELA-AU 15 50766040 50766040 single base substitution T G intron_variant MELA-AU 15 50766457 50766457 single base substitution C T downstream_gene_variant MELA-AU 15 50766457 50766457 single base substitution C T intron_variant MELA-AU 15 50768684 50768684 single base substitution G C downstream_gene_variant MELA-AU 15 50768684 50768684 single base substitution G C intron_variant MELA-AU 15 50769122 50769122 single base substitution C T 3_prime_UTR_variant MELA-AU 15 50769122 50769122 single base substitution C T exon_variant MELA-AU 15 50769122 50769122 single base substitution C T intron_variant MELA-AU 15 50769122 50769122 single base substitution C T missense_variant P232L 695C>T MELA-AU 15 50769122 50769122 single base substitution C T missense_variant P309L 926C>T MELA-AU 15 50769252 50769252 single base substitution C T intron_variant MELA-AU 15 50770519 50770519 single base substitution C T intron_variant MELA-AU 15 50771860 50771860 single base substitution T C intron_variant MELA-AU 15 50771990 50771990 single base substitution C T intron_variant MELA-AU 15 50773069 50773069 single base substitution C T intron_variant MELA-AU 15 50773684 50773684 single base substitution C T 3_prime_UTR_variant MELA-AU 15 50773684 50773684 single base substitution C T exon_variant MELA-AU 15 50773684 50773684 single base substitution C T missense_variant R332C 994C>T MELA-AU 15 50773684 50773684 single base substitution C T missense_variant R409C 1225C>T MELA-AU 15 50774834 50774834 deletion of <=200bp T - downstream_gene_variant MELA-AU 15 50774834 50774834 deletion of <=200bp T - intron_variant MELA-AU 15 50774984 50774984 single base substitution G A downstream_gene_variant MELA-AU 15 50774984 50774984 single base substitution G A intron_variant MELA-AU 15 50776569 50776569 single base substitution T C downstream_gene_variant MELA-AU 15 50776569 50776569 single base substitution T C intron_variant MELA-AU 15 50777012 50777012 single base substitution G A downstream_gene_variant MELA-AU 15 50777012 50777012 single base substitution G A intron_variant MELA-AU 15 50777012 50777012 single base substitution G A upstream_gene_variant MELA-AU 15 50779128 50779128 single base substitution G A intron_variant MELA-AU 15 50779128 50779128 single base substitution G A upstream_gene_variant MELA-AU 15 50779579 50779579 single base substitution G C intron_variant MELA-AU 15 50779579 50779579 single base substitution G C upstream_gene_variant MELA-AU 15 50782205 50782205 single base substitution C T intron_variant MELA-AU 15 50782205 50782205 single base substitution C T upstream_gene_variant MELA-AU 15 50783300 50783300 single base substitution C T downstream_gene_variant MELA-AU 15 50783300 50783300 single base substitution C T intron_variant MELA-AU 15 50783300 50783300 single base substitution C T upstream_gene_variant MELA-AU 15 50783609 50783609 single base substitution A G downstream_gene_variant MELA-AU 15 50783609 50783609 single base substitution A G intron_variant MELA-AU 15 50783609 50783609 single base substitution A G upstream_gene_variant MELA-AU 15 50784927 50784927 single base substitution C T downstream_gene_variant MELA-AU 15 50784927 50784927 single base substitution C T missense_variant S649L 1946C>T MELA-AU 15 50784927 50784927 single base substitution C T missense_variant S755L 2264C>T MELA-AU 15 50784927 50784927 single base substitution C T upstream_gene_variant MELA-AU 15 50785385 50785385 single base substitution C T downstream_gene_variant MELA-AU 15 50785385 50785385 single base substitution C T exon_variant MELA-AU 15 50785385 50785385 single base substitution C T intron_variant MELA-AU 15 50785386 50785386 single base substitution C T downstream_gene_variant MELA-AU 15 50785386 50785386 single base substitution C T exon_variant MELA-AU 15 50785386 50785386 single base substitution C T intron_variant MELA-AU 15 50785778 50785778 single base substitution C T downstream_gene_variant MELA-AU 15 50785778 50785778 single base substitution C T exon_variant MELA-AU 15 50785778 50785778 single base substitution C T intron_variant MELA-AU 15 50785778 50785778 single base substitution C T upstream_gene_variant MELA-AU 15 50786460 50786460 single base substitution C T downstream_gene_variant MELA-AU 15 50786460 50786460 single base substitution C T exon_variant MELA-AU 15 50786460 50786460 single base substitution C T missense_variant H775Y 2323C>T MELA-AU 15 50786460 50786460 single base substitution C T missense_variant H881Y 2641C>T MELA-AU 15 50786460 50786460 single base substitution C T upstream_gene_variant MELA-AU 15 50786512 50786512 single base substitution C T downstream_gene_variant MELA-AU 15 50786512 50786512 single base substitution C T intron_variant MELA-AU 15 50786512 50786512 single base substitution C T upstream_gene_variant MELA-AU 15 50787594 50787595 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 15 50787594 50787595 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 15 50787594 50787595 multiple base substitution (>=2bp and <=200bp) CC AT upstream_gene_variant MELA-AU 15 50787834 50787834 single base substitution C T intron_variant MELA-AU 15 50787834 50787834 single base substitution C T upstream_gene_variant MELA-AU 15 50789056 50789056 single base substitution C T intron_variant MELA-AU 15 50789056 50789056 single base substitution C T upstream_gene_variant MELA-AU 15 50789116 50789116 single base substitution C T intron_variant MELA-AU 15 50789116 50789116 single base substitution C T upstream_gene_variant MELA-AU 15 50789895 50789895 single base substitution C T intron_variant MELA-AU 15 50789895 50789895 single base substitution C T upstream_gene_variant MELA-AU 15 50790317 50790317 single base substitution C T intron_variant MELA-AU 15 50790317 50790317 single base substitution C T upstream_gene_variant MELA-AU 15 50790657 50790657 single base substitution C T intron_variant MELA-AU 15 50790657 50790657 single base substitution C T upstream_gene_variant MELA-AU 15 50790683 50790683 single base substitution T G intron_variant MELA-AU 15 50790683 50790683 single base substitution T G upstream_gene_variant MELA-AU 15 50790924 50790924 single base substitution C T missense_variant S1057L 3170C>T MELA-AU 15 50790924 50790924 single base substitution C T missense_variant S951L 2852C>T MELA-AU 15 50790924 50790924 single base substitution C T splice_region_variant MELA-AU 15 50791491 50791491 single base substitution A T 3_prime_UTR_variant MELA-AU 15 50791491 50791491 single base substitution A T exon_variant MELA-AU 15 50791499 50791499 single base substitution C G 3_prime_UTR_variant MELA-AU 15 50791499 50791499 single base substitution C G exon_variant MELA-AU 15 50791537 50791537 deletion of <=200bp T - 3_prime_UTR_variant MELA-AU 15 50791537 50791537 deletion of <=200bp T - exon_variant MELA-AU 15 50791585 50791585 single base substitution C T 3_prime_UTR_variant MELA-AU 15 50791585 50791585 single base substitution C T exon_variant MELA-AU 15 50794051 50794051 single base substitution C A downstream_gene_variant MELA-AU 15 50794109 50794109 single base substitution C T downstream_gene_variant MELA-AU 15 50794139 50794139 single base substitution C A downstream_gene_variant MELA-AU 15 50794208 50794208 single base substitution C T downstream_gene_variant MELA-AU 15 50794333 50794333 single base substitution C T downstream_gene_variant MELA-AU 15 50794403 50794403 single base substitution C T downstream_gene_variant MELA-AU 15 50794883 50794883 single base substitution C T downstream_gene_variant MELA-AU 15 50794952 50794952 single base substitution C T downstream_gene_variant MELA-AU 15 50794987 50794987 single base substitution G A downstream_gene_variant MELA-AU 15 50796279 50796279 single base substitution G A downstream_gene_variant MELA-AU 15 50796530 50796530 single base substitution C T downstream_gene_variant MELA-AU 15 50797865 50797865 single base substitution T A downstream_gene_variant MELA-AU 15 50798185 50798185 single base substitution T A downstream_gene_variant ORCA-IN 15 50755364 50755364 single base substitution C T downstream_gene_variant ORCA-IN 15 50755364 50755364 single base substitution C T intron_variant ORCA-IN 15 50782488 50782488 single base substitution G A exon_variant ORCA-IN 15 50782488 50782488 single base substitution G A missense_variant R561H 1682G>A ORCA-IN 15 50782488 50782488 single base substitution G A missense_variant R667H 2000G>A ORCA-IN 15 50782488 50782488 single base substitution G A upstream_gene_variant ORCA-IN 15 50787435 50787492 deletion of <=200bp ATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - downstream_gene_variant ORCA-IN 15 50787435 50787492 deletion of <=200bp ATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - intron_variant ORCA-IN 15 50787435 50787492 deletion of <=200bp ATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - upstream_gene_variant OV-AU 15 50716270 50716270 single base substitution C G upstream_gene_variant OV-AU 15 50716567 50716567 single base substitution G A upstream_gene_variant OV-AU 15 50721035 50721035 single base substitution A C intron_variant OV-AU 15 50724042 50724042 single base substitution G C intron_variant OV-AU 15 50727875 50727875 single base substitution A G intron_variant OV-AU 15 50727875 50727875 single base substitution A G upstream_gene_variant OV-AU 15 50730110 50730110 single base substitution A G intron_variant OV-AU 15 50730110 50730110 single base substitution A G upstream_gene_variant OV-AU 15 50730122 50730122 single base substitution G A intron_variant OV-AU 15 50730122 50730122 single base substitution G A upstream_gene_variant OV-AU 15 50730236 50730236 single base substitution C G intron_variant OV-AU 15 50730236 50730236 single base substitution C G upstream_gene_variant OV-AU 15 50737450 50737450 single base substitution T C downstream_gene_variant OV-AU 15 50737450 50737450 single base substitution T C intron_variant OV-AU 15 50737452 50737452 single base substitution A G downstream_gene_variant OV-AU 15 50737452 50737452 single base substitution A G intron_variant OV-AU 15 50743162 50743162 single base substitution G C downstream_gene_variant OV-AU 15 50743162 50743162 single base substitution G C intron_variant OV-AU 15 50748523 50748523 single base substitution C A intron_variant OV-AU 15 50748523 50748523 single base substitution C A upstream_gene_variant OV-AU 15 50756212 50756212 single base substitution G A downstream_gene_variant OV-AU 15 50756212 50756212 single base substitution G A intron_variant OV-AU 15 50763963 50763963 single base substitution C A 3_prime_UTR_variant OV-AU 15 50763963 50763963 single base substitution C A downstream_gene_variant OV-AU 15 50763963 50763963 single base substitution C A exon_variant OV-AU 15 50763963 50763963 single base substitution C A intron_variant OV-AU 15 50763963 50763963 single base substitution C A missense_variant L197I 589C>A OV-AU 15 50763963 50763963 single base substitution C A missense_variant L274I 820C>A OV-AU 15 50774576 50774576 single base substitution A G downstream_gene_variant OV-AU 15 50774576 50774576 single base substitution A G intron_variant OV-AU 15 50791846 50791846 single base substitution T G 3_prime_UTR_variant OV-AU 15 50791846 50791846 single base substitution T G downstream_gene_variant OV-AU 15 50791846 50791846 single base substitution T G exon_variant PACA-AU 15 50716990 50716990 single base substitution T C intron_variant PACA-AU 15 50716990 50716990 single base substitution T C upstream_gene_variant PACA-AU 15 50730350 50730350 single base substitution G A intron_variant PACA-AU 15 50730350 50730350 single base substitution G A upstream_gene_variant PACA-AU 15 50732029 50732029 single base substitution T A intron_variant PACA-AU 15 50733640 50733640 single base substitution G A exon_variant PACA-AU 15 50733640 50733640 single base substitution G A intron_variant PACA-AU 15 50733640 50733640 single base substitution G A missense_variant V67M 199G>A PACA-AU 15 50733661 50733661 deletion of <=200bp A - downstream_gene_variant PACA-AU 15 50733661 50733661 deletion of <=200bp A - exon_variant PACA-AU 15 50733661 50733661 deletion of <=200bp A - frameshift_variant K74 PACA-AU 15 50733661 50733661 deletion of <=200bp A - intron_variant PACA-AU 15 50737271 50737271 insertion of <=200bp - T downstream_gene_variant PACA-AU 15 50737271 50737271 insertion of <=200bp - T intron_variant PACA-AU 15 50737472 50737472 single base substitution A G downstream_gene_variant PACA-AU 15 50737472 50737472 single base substitution A G intron_variant PACA-AU 15 50738444 50738444 single base substitution A C downstream_gene_variant PACA-AU 15 50738444 50738444 single base substitution A C intron_variant PACA-AU 15 50741523 50741523 single base substitution T G downstream_gene_variant PACA-AU 15 50741523 50741523 single base substitution T G intron_variant PACA-AU 15 50742091 50742091 single base substitution T C downstream_gene_variant PACA-AU 15 50742091 50742091 single base substitution T C intron_variant PACA-AU 15 50742092 50742092 single base substitution T C downstream_gene_variant PACA-AU 15 50742092 50742092 single base substitution T C intron_variant PACA-AU 15 50757556 50757556 deletion of <=200bp G - downstream_gene_variant PACA-AU 15 50757556 50757556 deletion of <=200bp G - intron_variant PACA-AU 15 50758370 50758370 single base substitution C G downstream_gene_variant PACA-AU 15 50758370 50758370 single base substitution C G intron_variant PACA-AU 15 50765117 50765117 single base substitution C A downstream_gene_variant PACA-AU 15 50765117 50765117 single base substitution C A intron_variant PACA-AU 15 50767710 50767710 single base substitution C T downstream_gene_variant PACA-AU 15 50767710 50767710 single base substitution C T intron_variant PACA-AU 15 50774748 50774748 single base substitution A C downstream_gene_variant PACA-AU 15 50774748 50774748 single base substitution A C intron_variant PACA-AU 15 50775611 50775611 single base substitution T A downstream_gene_variant PACA-AU 15 50775611 50775611 single base substitution T A intron_variant PACA-AU 15 50775612 50775612 single base substitution A T downstream_gene_variant PACA-AU 15 50775612 50775612 single base substitution A T intron_variant PACA-AU 15 50776292 50776308 deletion of <=200bp AGTTCTTTAGTTTTTTA - downstream_gene_variant PACA-AU 15 50776292 50776308 deletion of <=200bp AGTTCTTTAGTTTTTTA - intron_variant PACA-AU 15 50781973 50781973 single base substitution A T exon_variant PACA-AU 15 50781973 50781973 single base substitution A T intron_variant PACA-AU 15 50781973 50781973 single base substitution A T upstream_gene_variant PACA-CA 15 50712805 50712805 single base substitution G A upstream_gene_variant PACA-CA 15 50713335 50713335 single base substitution C T upstream_gene_variant PACA-CA 15 50715470 50715470 single base substitution T A upstream_gene_variant PACA-CA 15 50716480 50716480 single base substitution A T upstream_gene_variant PACA-CA 15 50717821 50717821 single base substitution T C intron_variant PACA-CA 15 50717821 50717821 single base substitution T C upstream_gene_variant PACA-CA 15 50727307 50727307 single base substitution C T intron_variant PACA-CA 15 50727307 50727307 single base substitution C T upstream_gene_variant PACA-CA 15 50727953 50727953 single base substitution G A intron_variant PACA-CA 15 50727953 50727953 single base substitution G A upstream_gene_variant PACA-CA 15 50733174 50733174 single base substitution G T intron_variant PACA-CA 15 50734784 50734784 insertion of <=200bp - A downstream_gene_variant PACA-CA 15 50734784 50734784 insertion of <=200bp - A intron_variant PACA-CA 15 50741353 50741353 single base substitution T G downstream_gene_variant PACA-CA 15 50741353 50741353 single base substitution T G intron_variant PACA-CA 15 50741519 50741519 single base substitution G T downstream_gene_variant PACA-CA 15 50741519 50741519 single base substitution G T intron_variant PACA-CA 15 50742157 50742157 single base substitution C T downstream_gene_variant PACA-CA 15 50742157 50742157 single base substitution C T intron_variant PACA-CA 15 50743375 50743375 single base substitution C T downstream_gene_variant PACA-CA 15 50743375 50743375 single base substitution C T intron_variant PACA-CA 15 50750887 50750887 single base substitution T G intron_variant PACA-CA 15 50752285 50752285 single base substitution C G downstream_gene_variant PACA-CA 15 50752285 50752285 single base substitution C G intron_variant PACA-CA 15 50752790 50752790 single base substitution G A downstream_gene_variant PACA-CA 15 50752790 50752790 single base substitution G A intron_variant PACA-CA 15 50756018 50756020 deletion of <=200bp ACT - downstream_gene_variant PACA-CA 15 50756018 50756020 deletion of <=200bp ACT - intron_variant PACA-CA 15 50766897 50766898 deletion of <=200bp TC - downstream_gene_variant PACA-CA 15 50766897 50766898 deletion of <=200bp TC - intron_variant PACA-CA 15 50767783 50767783 single base substitution C T downstream_gene_variant PACA-CA 15 50767783 50767783 single base substitution C T intron_variant PACA-CA 15 50769124 50769124 single base substitution C T 3_prime_UTR_variant PACA-CA 15 50769124 50769124 single base substitution C T exon_variant PACA-CA 15 50769124 50769124 single base substitution C T intron_variant PACA-CA 15 50769124 50769124 single base substitution C T stop_gained Q233* 697C>T PACA-CA 15 50769124 50769124 single base substitution C T stop_gained Q310* 928C>T PACA-CA 15 50776588 50776588 deletion of <=200bp A - downstream_gene_variant PACA-CA 15 50776588 50776588 deletion of <=200bp A - intron_variant PACA-CA 15 50778814 50778814 deletion of <=200bp A - downstream_gene_variant PACA-CA 15 50778814 50778814 deletion of <=200bp A - intron_variant PACA-CA 15 50778814 50778814 deletion of <=200bp A - upstream_gene_variant PACA-CA 15 50781962 50781962 single base substitution A T exon_variant PACA-CA 15 50781962 50781962 single base substitution A T intron_variant PACA-CA 15 50781962 50781962 single base substitution A T upstream_gene_variant PACA-CA 15 50781972 50781972 single base substitution A T exon_variant PACA-CA 15 50781972 50781972 single base substitution A T intron_variant PACA-CA 15 50781972 50781972 single base substitution A T upstream_gene_variant PACA-CA 15 50782456 50782456 single base substitution T A intron_variant PACA-CA 15 50782456 50782456 single base substitution T A splice_region_variant PACA-CA 15 50782456 50782456 single base substitution T A upstream_gene_variant PACA-CA 15 50785151 50785151 single base substitution G C downstream_gene_variant PACA-CA 15 50785151 50785151 single base substitution G C intron_variant PACA-CA 15 50785151 50785151 single base substitution G C upstream_gene_variant PACA-CA 15 50794198 50794198 single base substitution C A downstream_gene_variant PACA-CA 15 50798195 50798195 single base substitution G C downstream_gene_variant PAEN-AU 15 50751916 50751916 single base substitution A G downstream_gene_variant PAEN-AU 15 50751916 50751916 single base substitution A G intron_variant PAEN-AU 15 50787680 50787680 single base substitution T G intron_variant PAEN-AU 15 50787680 50787680 single base substitution T G upstream_gene_variant PBCA-DE 15 50711636 50711637 deletion of <=200bp AC - upstream_gene_variant PBCA-DE 15 50714666 50714666 single base substitution T A upstream_gene_variant PBCA-DE 15 50717975 50717975 single base substitution C T intron_variant PBCA-DE 15 50717975 50717975 single base substitution C T upstream_gene_variant PBCA-DE 15 50727946 50727948 deletion of <=200bp ATT - intron_variant PBCA-DE 15 50727946 50727948 deletion of <=200bp ATT - upstream_gene_variant PBCA-DE 15 50749081 50749081 insertion of <=200bp - A intron_variant PBCA-DE 15 50749081 50749081 insertion of <=200bp - A upstream_gene_variant PBCA-DE 15 50750388 50750388 insertion of <=200bp - G intron_variant PBCA-DE 15 50750388 50750388 insertion of <=200bp - G upstream_gene_variant PBCA-DE 15 50752994 50752994 deletion of <=200bp T - downstream_gene_variant PBCA-DE 15 50752994 50752994 deletion of <=200bp T - intron_variant PBCA-DE 15 50760601 50760601 single base substitution G A downstream_gene_variant PBCA-DE 15 50760601 50760601 single base substitution G A intron_variant PBCA-DE 15 50772831 50772831 insertion of <=200bp - T intron_variant PBCA-DE 15 50778853 50778853 single base substitution C T downstream_gene_variant PBCA-DE 15 50778853 50778853 single base substitution C T intron_variant PBCA-DE 15 50778853 50778853 single base substitution C T upstream_gene_variant PBCA-DE 15 50781964 50781964 single base substitution T A exon_variant PBCA-DE 15 50781964 50781964 single base substitution T A intron_variant PBCA-DE 15 50781964 50781964 single base substitution T A upstream_gene_variant PBCA-DE 15 50784990 50784990 single base substitution T C downstream_gene_variant PBCA-DE 15 50784990 50784990 single base substitution T C missense_variant L670P 2009T>C PBCA-DE 15 50784990 50784990 single base substitution T C missense_variant L776P 2327T>C PBCA-DE 15 50784990 50784990 single base substitution T C upstream_gene_variant PBCA-DE 15 50786266 50786266 single base substitution G A downstream_gene_variant PBCA-DE 15 50786266 50786266 single base substitution G A exon_variant PBCA-DE 15 50786266 50786266 single base substitution G A splice_acceptor_variant PBCA-DE 15 50786266 50786266 single base substitution G A upstream_gene_variant PBCA-DE 15 50787387 50787388 deletion of <=200bp AT - downstream_gene_variant PBCA-DE 15 50787387 50787388 deletion of <=200bp AT - intron_variant PBCA-DE 15 50787387 50787388 deletion of <=200bp AT - upstream_gene_variant PBCA-DE 15 50788701 50788701 single base substitution T G intron_variant PBCA-DE 15 50788701 50788701 single base substitution T G upstream_gene_variant PRAD-CA 15 50722606 50722606 single base substitution A G intron_variant PRAD-CA 15 50733001 50733001 single base substitution A T intron_variant PRAD-CA 15 50745315 50745315 single base substitution G A downstream_gene_variant PRAD-CA 15 50745315 50745315 single base substitution G A intron_variant PRAD-CA 15 50750587 50750587 single base substitution A G intron_variant PRAD-CA 15 50750587 50750587 single base substitution A G upstream_gene_variant PRAD-CA 15 50778450 50778450 single base substitution C A downstream_gene_variant PRAD-CA 15 50778450 50778450 single base substitution C A intron_variant PRAD-CA 15 50778450 50778450 single base substitution C A upstream_gene_variant PRAD-CA 15 50795821 50795821 single base substitution G T downstream_gene_variant PRAD-UK 15 50715470 50715470 single base substitution T A upstream_gene_variant PRAD-UK 15 50719295 50719295 single base substitution C G intron_variant PRAD-UK 15 50722665 50722665 single base substitution A T intron_variant PRAD-UK 15 50750880 50750880 single base substitution T A intron_variant PRAD-UK 15 50752597 50752597 single base substitution G A downstream_gene_variant PRAD-UK 15 50752597 50752597 single base substitution G A intron_variant PRAD-UK 15 50756816 50756816 single base substitution C T downstream_gene_variant PRAD-UK 15 50756816 50756816 single base substitution C T intron_variant PRAD-UK 15 50758533 50758533 single base substitution C T downstream_gene_variant PRAD-UK 15 50758533 50758533 single base substitution C T intron_variant PRAD-UK 15 50758726 50758726 single base substitution A C downstream_gene_variant PRAD-UK 15 50758726 50758726 single base substitution A C intron_variant PRAD-UK 15 50775789 50775789 single base substitution A G downstream_gene_variant PRAD-UK 15 50775789 50775789 single base substitution A G intron_variant PRAD-UK 15 50782477 50782477 single base substitution T G exon_variant PRAD-UK 15 50782477 50782477 single base substitution T G synonymous_variant T557T 1671T>G PRAD-UK 15 50782477 50782477 single base substitution T G synonymous_variant T663T 1989T>G PRAD-UK 15 50782477 50782477 single base substitution T G upstream_gene_variant PRAD-UK 15 50791357 50791357 single base substitution T C 3_prime_UTR_variant PRAD-UK 15 50791357 50791357 single base substitution T C exon_variant PRAD-US 15 50788105 50788105 single base substitution G T exon_variant PRAD-US 15 50788105 50788105 single base substitution G T missense_variant A801S 2401G>T PRAD-US 15 50788105 50788105 single base substitution G T missense_variant A907S 2719G>T PRAD-US 15 50788105 50788105 single base substitution G T upstream_gene_variant PRAD-US 15 50790907 50790907 single base substitution T C exon_variant PRAD-US 15 50790907 50790907 single base substitution T C synonymous_variant Y1051Y 3153T>C PRAD-US 15 50790907 50790907 single base substitution T C synonymous_variant Y945Y 2835T>C RECA-EU 15 50722931 50722931 single base substitution A T intron_variant RECA-EU 15 50728049 50728049 single base substitution C T intron_variant RECA-EU 15 50728049 50728049 single base substitution C T upstream_gene_variant RECA-EU 15 50728989 50728989 single base substitution C A intron_variant RECA-EU 15 50728989 50728989 single base substitution C A upstream_gene_variant RECA-EU 15 50734162 50734162 single base substitution A G downstream_gene_variant RECA-EU 15 50734162 50734162 single base substitution A G intron_variant RECA-EU 15 50742724 50742724 single base substitution A T downstream_gene_variant RECA-EU 15 50742724 50742724 single base substitution A T intron_variant RECA-EU 15 50747192 50747192 single base substitution C T intron_variant RECA-EU 15 50747192 50747192 single base substitution C T upstream_gene_variant RECA-EU 15 50786483 50786483 single base substitution A T downstream_gene_variant RECA-EU 15 50786483 50786483 single base substitution A T intron_variant RECA-EU 15 50786483 50786483 single base substitution A T splice_region_variant RECA-EU 15 50786483 50786483 single base substitution A T upstream_gene_variant SKCA-BR 15 50713982 50713982 single base substitution T C upstream_gene_variant SKCA-BR 15 50714052 50714052 single base substitution C T upstream_gene_variant SKCA-BR 15 50714080 50714080 single base substitution T G upstream_gene_variant SKCA-BR 15 50715387 50715387 single base substitution G A upstream_gene_variant SKCA-BR 15 50717023 50717023 insertion of <=200bp - GT intron_variant SKCA-BR 15 50717023 50717023 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 15 50720828 50720846 deletion of <=200bp ATATAGTGTAATAAAAGTT - intron_variant SKCA-BR 15 50721613 50721613 single base substitution C T intron_variant SKCA-BR 15 50722055 50722055 single base substitution C T intron_variant SKCA-BR 15 50723887 50723887 single base substitution C T intron_variant SKCA-BR 15 50725647 50725647 single base substitution T G intron_variant SKCA-BR 15 50725992 50725992 single base substitution C T intron_variant SKCA-BR 15 50726023 50726023 single base substitution T C intron_variant SKCA-BR 15 50726182 50726182 single base substitution C T intron_variant SKCA-BR 15 50739283 50739283 single base substitution A T downstream_gene_variant SKCA-BR 15 50739283 50739283 single base substitution A T intron_variant SKCA-BR 15 50741505 50741505 single base substitution T C downstream_gene_variant SKCA-BR 15 50741505 50741505 single base substitution T C intron_variant SKCA-BR 15 50746057 50746057 insertion of <=200bp - CTT downstream_gene_variant SKCA-BR 15 50746057 50746057 insertion of <=200bp - CTT intron_variant SKCA-BR 15 50746057 50746057 insertion of <=200bp - CTT upstream_gene_variant SKCA-BR 15 50746402 50746402 single base substitution C T downstream_gene_variant SKCA-BR 15 50746402 50746402 single base substitution C T intron_variant SKCA-BR 15 50746402 50746402 single base substitution C T upstream_gene_variant SKCA-BR 15 50748651 50748651 single base substitution T C intron_variant SKCA-BR 15 50748651 50748651 single base substitution T C upstream_gene_variant SKCA-BR 15 50749795 50749795 single base substitution C T intron_variant SKCA-BR 15 50749795 50749795 single base substitution C T upstream_gene_variant SKCA-BR 15 50751529 50751529 single base substitution C T downstream_gene_variant SKCA-BR 15 50751529 50751529 single base substitution C T intron_variant SKCA-BR 15 50752193 50752193 insertion of <=200bp - CCT downstream_gene_variant SKCA-BR 15 50752193 50752193 insertion of <=200bp - CCT intron_variant SKCA-BR 15 50754367 50754367 single base substitution C G downstream_gene_variant SKCA-BR 15 50754367 50754367 single base substitution C G intron_variant SKCA-BR 15 50754778 50754778 single base substitution C T downstream_gene_variant SKCA-BR 15 50754778 50754778 single base substitution C T intron_variant SKCA-BR 15 50757920 50757920 single base substitution C T downstream_gene_variant SKCA-BR 15 50757920 50757920 single base substitution C T intron_variant SKCA-BR 15 50759064 50759064 single base substitution C T downstream_gene_variant SKCA-BR 15 50759064 50759064 single base substitution C T intron_variant SKCA-BR 15 50761703 50761703 single base substitution C T downstream_gene_variant SKCA-BR 15 50761703 50761703 single base substitution C T intron_variant SKCA-BR 15 50767966 50767966 single base substitution A T downstream_gene_variant SKCA-BR 15 50767966 50767966 single base substitution A T intron_variant SKCA-BR 15 50771059 50771059 single base substitution C A intron_variant SKCA-BR 15 50777646 50777646 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 15 50777646 50777646 insertion of <=200bp - CA intron_variant SKCA-BR 15 50777646 50777646 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 15 50777747 50777759 deletion of <=200bp ATTTTTTTTTTTT - downstream_gene_variant SKCA-BR 15 50777747 50777759 deletion of <=200bp ATTTTTTTTTTTT - intron_variant SKCA-BR 15 50777747 50777759 deletion of <=200bp ATTTTTTTTTTTT - upstream_gene_variant SKCA-BR 15 50782836 50782836 single base substitution A C downstream_gene_variant SKCA-BR 15 50782836 50782836 single base substitution A C intron_variant SKCA-BR 15 50782836 50782836 single base substitution A C upstream_gene_variant SKCA-BR 15 50787434 50787492 deletion of <=200bp TATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - downstream_gene_variant SKCA-BR 15 50787434 50787492 deletion of <=200bp TATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - intron_variant SKCA-BR 15 50787434 50787492 deletion of <=200bp TATATATACGTGTATATATACATACATATATACACATATATATACACATACATATATAC - upstream_gene_variant SKCA-BR 15 50788603 50788603 single base substitution T G intron_variant SKCA-BR 15 50788603 50788603 single base substitution T G upstream_gene_variant SKCA-BR 15 50788966 50788966 single base substitution A G intron_variant SKCA-BR 15 50788966 50788966 single base substitution A G upstream_gene_variant SKCA-BR 15 50789408 50789408 single base substitution G A exon_variant SKCA-BR 15 50789408 50789408 single base substitution G A synonymous_variant V1006V 3018G>A SKCA-BR 15 50789408 50789408 single base substitution G A synonymous_variant V900V 2700G>A SKCA-BR 15 50789408 50789408 single base substitution G A upstream_gene_variant SKCM-US 15 50733667 50733667 single base substitution A T downstream_gene_variant SKCM-US 15 50733667 50733667 single base substitution A T exon_variant SKCM-US 15 50733667 50733667 single base substitution A T intron_variant SKCM-US 15 50733667 50733667 single base substitution A T stop_gained R76* 226A>T SKCM-US 15 50741605 50741605 single base substitution C T downstream_gene_variant SKCM-US 15 50741605 50741605 single base substitution C T exon_variant SKCM-US 15 50741605 50741605 single base substitution C T intron_variant SKCM-US 15 50741605 50741605 single base substitution C T synonymous_variant F86F 258C>T SKCM-US 15 50782062 50782062 single base substitution C T exon_variant SKCM-US 15 50782062 50782062 single base substitution C T missense_variant P546L 1637C>T SKCM-US 15 50782062 50782062 single base substitution C T missense_variant P652L 1955C>T SKCM-US 15 50782062 50782062 single base substitution C T upstream_gene_variant SKCM-US 15 50782595 50782595 single base substitution C T exon_variant SKCM-US 15 50782595 50782595 single base substitution C T missense_variant P597S 1789C>T SKCM-US 15 50782595 50782595 single base substitution C T missense_variant P703S 2107C>T SKCM-US 15 50782595 50782595 single base substitution C T upstream_gene_variant SKCM-US 15 50782635 50782635 single base substitution C T downstream_gene_variant SKCM-US 15 50782635 50782635 single base substitution C T missense_variant S610F 1829C>T SKCM-US 15 50782635 50782635 single base substitution C T missense_variant S716F 2147C>T SKCM-US 15 50782635 50782635 single base substitution C T upstream_gene_variant SKCM-US 15 50785001 50785001 single base substitution C T downstream_gene_variant SKCM-US 15 50785001 50785001 single base substitution C T missense_variant R674C 2020C>T SKCM-US 15 50785001 50785001 single base substitution C T missense_variant R780C 2338C>T SKCM-US 15 50785001 50785001 single base substitution C T upstream_gene_variant SKCM-US 15 50786292 50786292 single base substitution G A downstream_gene_variant SKCM-US 15 50786292 50786292 single base substitution G A exon_variant SKCM-US 15 50786292 50786292 single base substitution G A missense_variant E719K 2155G>A SKCM-US 15 50786292 50786292 single base substitution G A missense_variant E825K 2473G>A SKCM-US 15 50786292 50786292 single base substitution G A upstream_gene_variant SKCM-US 15 50786354 50786354 single base substitution C T downstream_gene_variant SKCM-US 15 50786354 50786354 single base substitution C T exon_variant SKCM-US 15 50786354 50786354 single base substitution C T synonymous_variant I739I 2217C>T SKCM-US 15 50786354 50786354 single base substitution C T synonymous_variant I845I 2535C>T SKCM-US 15 50786354 50786354 single base substitution C T upstream_gene_variant SKCM-US 15 50788176 50788176 single base substitution C T exon_variant SKCM-US 15 50788176 50788176 single base substitution C T synonymous_variant F824F 2472C>T SKCM-US 15 50788176 50788176 single base substitution C T synonymous_variant F930F 2790C>T SKCM-US 15 50788176 50788176 single base substitution C T upstream_gene_variant SKCM-US 15 50791221 50791221 single base substitution C T exon_variant SKCM-US 15 50791221 50791221 single base substitution C T missense_variant S1098F 3293C>T SKCM-US 15 50791221 50791221 single base substitution C T missense_variant S992F 2975C>T STAD-US 15 50733661 50733661 deletion of <=200bp A - downstream_gene_variant STAD-US 15 50733661 50733661 deletion of <=200bp A - exon_variant STAD-US 15 50733661 50733661 deletion of <=200bp A - frameshift_variant K74 STAD-US 15 50733661 50733661 deletion of <=200bp A - intron_variant STAD-US 15 50763891 50763891 insertion of <=200bp - G 3_prime_UTR_variant STAD-US 15 50763891 50763891 insertion of <=200bp - G exon_variant STAD-US 15 50763891 50763891 insertion of <=200bp - G frameshift_variant R173E? STAD-US 15 50763891 50763891 insertion of <=200bp - G frameshift_variant R250E? STAD-US 15 50763891 50763891 insertion of <=200bp - G intron_variant STAD-US 15 50763892 50763892 insertion of <=200bp - G 3_prime_UTR_variant STAD-US 15 50763892 50763892 insertion of <=200bp - G exon_variant STAD-US 15 50763892 50763892 insertion of <=200bp - G frameshift_variant R173R? STAD-US 15 50763892 50763892 insertion of <=200bp - G frameshift_variant R250R? STAD-US 15 50763892 50763892 insertion of <=200bp - G intron_variant STAD-US 15 50769071 50769071 single base substitution A G 3_prime_UTR_variant STAD-US 15 50769071 50769071 single base substitution A G exon_variant STAD-US 15 50769071 50769071 single base substitution A G intron_variant STAD-US 15 50769071 50769071 single base substitution A G missense_variant N215S 644A>G STAD-US 15 50769071 50769071 single base substitution A G missense_variant N292S 875A>G STAD-US 15 50774185 50774185 single base substitution C A downstream_gene_variant STAD-US 15 50774185 50774185 single base substitution C A missense_variant P499T 1495C>A STAD-US 15 50774185 50774185 single base substitution C A missense_variant P576T 1726C>A STAD-US 15 50782631 50782631 single base substitution C T downstream_gene_variant STAD-US 15 50782631 50782631 single base substitution C T missense_variant R609C 1825C>T STAD-US 15 50782631 50782631 single base substitution C T missense_variant R715C 2143C>T STAD-US 15 50782631 50782631 single base substitution C T upstream_gene_variant STAD-US 15 50785029 50785029 single base substitution A G downstream_gene_variant STAD-US 15 50785029 50785029 single base substitution A G missense_variant N683S 2048A>G STAD-US 15 50785029 50785029 single base substitution A G missense_variant N789S 2366A>G STAD-US 15 50785029 50785029 single base substitution A G upstream_gene_variant STAD-US 15 50791187 50791187 single base substitution G C exon_variant STAD-US 15 50791187 50791187 single base substitution G C missense_variant E1087Q 3259G>C STAD-US 15 50791187 50791187 single base substitution G C missense_variant E981Q 2941G>C THCA-SA 15 50776525 50776525 single base substitution T C downstream_gene_variant THCA-SA 15 50776525 50776525 single base substitution T C intron_variant THCA-SA 15 50776525 50776525 single base substitution T C synonymous_variant F619F 1857T>C THCA-SA 15 50784950 50784950 single base substitution C T downstream_gene_variant THCA-SA 15 50784950 50784950 single base substitution C T missense_variant R657W 1969C>T THCA-SA 15 50784950 50784950 single base substitution C T missense_variant R763W 2287C>T THCA-SA 15 50784950 50784950 single base substitution C T upstream_gene_variant THCA-SA 15 50785054 50785054 single base substitution C T downstream_gene_variant THCA-SA 15 50785054 50785054 single base substitution C T synonymous_variant N691N 2073C>T THCA-SA 15 50785054 50785054 single base substitution C T synonymous_variant N797N 2391C>T THCA-SA 15 50785054 50785054 single base substitution C T upstream_gene_variant THCA-SA 15 50785055 50785055 single base substitution G C downstream_gene_variant THCA-SA 15 50785055 50785055 single base substitution G C missense_variant A692P 2074G>C THCA-SA 15 50785055 50785055 single base substitution G C missense_variant A798P 2392G>C THCA-SA 15 50785055 50785055 single base substitution G C upstream_gene_variant UCEC-US 15 50731298 50731298 single base substitution G T exon_variant UCEC-US 15 50731298 50731298 single base substitution G T intron_variant UCEC-US 15 50731298 50731298 single base substitution G T stop_gained E10* 28G>T UCEC-US 15 50751197 50751197 single base substitution A T intron_variant UCEC-US 15 50751197 50751197 single base substitution A T missense_variant R112S 336A>T UCEC-US 15 50751197 50751197 single base substitution A T missense_variant R35S 105A>T UCEC-US 15 50751197 50751197 single base substitution A T splice_region_variant UCEC-US 15 50751275 50751275 single base substitution G A 3_prime_UTR_variant UCEC-US 15 50751275 50751275 single base substitution G A downstream_gene_variant UCEC-US 15 50751275 50751275 single base substitution G A exon_variant UCEC-US 15 50751275 50751275 single base substitution G A intron_variant UCEC-US 15 50751275 50751275 single base substitution G A synonymous_variant R138R 414G>A UCEC-US 15 50751275 50751275 single base substitution G A synonymous_variant R61R 183G>A UCEC-US 15 50769531 50769531 single base substitution G A 3_prime_UTR_variant UCEC-US 15 50769531 50769531 single base substitution G A exon_variant UCEC-US 15 50769531 50769531 single base substitution G A synonymous_variant T274T 822G>A UCEC-US 15 50769531 50769531 single base substitution G A synonymous_variant T351T 1053G>A UCEC-US 15 50769543 50769543 single base substitution T C 3_prime_UTR_variant UCEC-US 15 50769543 50769543 single base substitution T C exon_variant UCEC-US 15 50769543 50769543 single base substitution T C synonymous_variant S278S 834T>C UCEC-US 15 50769543 50769543 single base substitution T C synonymous_variant S355S 1065T>C UCEC-US 15 50773789 50773789 single base substitution C T 3_prime_UTR_variant UCEC-US 15 50773789 50773789 single base substitution C T exon_variant UCEC-US 15 50773789 50773789 single base substitution C T missense_variant R367C 1099C>T UCEC-US 15 50773789 50773789 single base substitution C T missense_variant R444C 1330C>T UCEC-US 15 50773906 50773906 single base substitution C T downstream_gene_variant UCEC-US 15 50773906 50773906 single base substitution C T missense_variant R406W 1216C>T UCEC-US 15 50773906 50773906 single base substitution C T missense_variant R483W 1447C>T UCEC-US 15 50773935 50773935 single base substitution G T downstream_gene_variant UCEC-US 15 50773935 50773935 single base substitution G T missense_variant E415D 1245G>T UCEC-US 15 50773935 50773935 single base substitution G T missense_variant E492D 1476G>T UCEC-US 15 50782026 50782026 single base substitution G A exon_variant UCEC-US 15 50782026 50782026 single base substitution G A missense_variant R534Q 1601G>A UCEC-US 15 50782026 50782026 single base substitution G A missense_variant R640Q 1919G>A UCEC-US 15 50782026 50782026 single base substitution G A upstream_gene_variant UCEC-US 15 50788072 50788072 single base substitution G T exon_variant UCEC-US 15 50788072 50788072 single base substitution G T stop_gained E790* 2368G>T UCEC-US 15 50788072 50788072 single base substitution G T stop_gained E896* 2686G>T UCEC-US 15 50788072 50788072 single base substitution G T upstream_gene_variant UCEC-US 15 50788200 50788200 single base substitution A G exon_variant UCEC-US 15 50788200 50788200 single base substitution A G synonymous_variant T832T 2496A>G UCEC-US 15 50788200 50788200 single base substitution A G synonymous_variant T938T 2814A>G UCEC-US 15 50788200 50788200 single base substitution A G upstream_gene_variant UCEC-US 15 50789404 50789404 single base substitution C T exon_variant UCEC-US 15 50789404 50789404 single base substitution C T missense_variant P1005L 3014C>T UCEC-US 15 50789404 50789404 single base substitution C T missense_variant P899L 2696C>T UCEC-US 15 50789404 50789404 single base substitution C T upstream_gene_variant UCEC-US 15 50790820 50790820 single base substitution A C exon_variant UCEC-US 15 50790820 50790820 single base substitution A C missense_variant Q1022H 3066A>C UCEC-US 15 50790820 50790820 single base substitution A C missense_variant Q916H 2748A>C UCEC-US 15 50790857 50790857 single base substitution C A exon_variant UCEC-US 15 50790857 50790857 single base substitution C A missense_variant L1035I 3103C>A UCEC-US 15 50790857 50790857 single base substitution C A missense_variant L929I 2785C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-C8-A26Y-01 COSM3816284 c.424G>A p.G142R Substitution - Missense 15:50459088-50459088 + 5-RS COSM1731733 c.2153C>G p.S718C Substitution - Missense 15:50490444-50490444 + TCGA-B5-A0JY-01 COSM962546 c.28G>T p.E10* Substitution - Nonsense 15:50439101-50439101 + PTC-28C COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + PT31 COSM5906968 c.2203A>G p.T735A Substitution - Missense 15:50490494-50490494 + HCT15 COSM2216610 c.3119A>G p.Y1040C Substitution - Missense 15:50498676-50498676 + B105-0 COSM1749198 c.2159C>G p.P720R Substitution - Missense 15:50490450-50490450 + T1204 COSM4739954 c.2772A>T p.A924A Substitution - coding silent 15:50495961-50495961 + 9102_T COSM5041522 c.365T>G p.L122R Substitution - Missense 15:50459029-50459029 + PT15_1 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-24-1564-01 COSM117603 c.578C>T p.T193M Substitution - Missense 15:50465083-50465083 + PTC_248 COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + TCGA-OL-A66K-01 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + tumor_4177601 COSM3356738 c.2165T>A p.I722K Substitution - Missense 15:50490456-50490456 + Br27P COSM40741 c.237C>T p.F79F Substitution - coding silent 15:50441481-50441481 + TCGA-42-2582-01 COSM1323164 c.1125G>A p.L375L Substitution - coding silent 15:50477406-50477406 + CSCC-27-T COSM4513064 c.925C>T p.P309S Substitution - Missense 15:50476924-50476924 + Single_Sample COSM1562903 c.2295C>A p.L765L Substitution - coding silent 15:50492761-50492761 + TCGA-66-2782-01 COSM701090 c.168G>A p.E56E Substitution - coding silent 15:50441412-50441412 + 35M COSM5583016 c.830T>C p.L277P Substitution - Missense 15:50471776-50471776 + ESO-580 COSM1270119 c.177C>G p.A59A Substitution - coding silent 15:50441421-50441421 + CHC361TA COSM2216600 c.2531A>G p.Y844C Substitution - Missense 15:50494153-50494153 + LC_S29 COSM1189004 c.1753A>G p.T585A Substitution - Missense 15:50482015-50482015 + ESCC_142 COSM5643697 c.1226G>A p.R409H Substitution - Missense 15:50481488-50481488 + Single_Sample COSM215607 c.2327T>C p.L776P Substitution - Missense 15:50492793-50492793 + KM12 COSM1373364 c.219_220insA p.R76fs*3 Insertion - Frameshift 15:50441463-50441464 + cSCCP5 COSM138063 c.1859G>A p.R620K Substitution - Missense 15:50484330-50484330 + SW403 COSM4655231 c.317C>A p.S106Y Substitution - Missense 15:50449467-50449467 + YUKAT COSM5383472 c.1935G>A p.G645G Substitution - coding silent 15:50489845-50489845 + 5-RSII COSM1731733 c.2153C>G p.S718C Substitution - Missense 15:50490444-50490444 + TCGA-QU-A6IN-01 COSM4876839 c.2719G>T p.A907S Substitution - Missense 15:50495908-50495908 + LN18 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-D1-A17M-01 COSM962550 c.336A>T p.R112S Substitution - Missense 15:50459000-50459000 + TCGA-EE-A2MR-06 COSM3501988 c.2790C>T p.F930F Substitution - coding silent 15:50495979-50495979 + TARGET-30-PARVNT COSM1288872 c.169G>A p.E57K Substitution - Missense 15:50441413-50441413 + TCGA-14-0862-01 COSM3401807 c.2712T>C p.F904F Substitution - coding silent 15:50495901-50495901 + C004 COSM5521967 c.3275C>T p.S1092F Substitution - Missense 15:50499006-50499006 + TCGA-DK-A3WW-01 COSM3794231 c.1206G>A p.K402K Substitution - coding silent 15:50477487-50477487 + AOCS-088-3-8 COSM3981552 c.820C>A p.L274I Substitution - Missense 15:50471766-50471766 + ESO-135 COSM1270118 c.1909A>T p.T637S Substitution - Missense 15:50489819-50489819 + P05-3436 COSM248261 c.2062G>T p.A688S Substitution - Missense 15:50490353-50490353 + ME009T COSM223766 c.31C>T p.L11F Substitution - Missense 15:50439104-50439104 + TCGA-AP-A059-01 COSM962570 c.3014C>T p.P1005L Substitution - Missense 15:50497207-50497207 + TCGA-DM-A28M-01 COSM404325 c.2353A>G p.T785A Substitution - Missense 15:50492819-50492819 + TCGA-AN-A046-01 COSM3816286 c.1441G>T p.E481* Substitution - Nonsense 15:50481703-50481703 + T3059 COSM4739953 c.2682A>C p.K894N Substitution - Missense 15:50495871-50495871 + TLE55 COSM215607 c.2327T>C p.L776P Substitution - Missense 15:50492793-50492793 + TCGA-AD-6889-01 COSM1373364 c.219_220insA p.R76fs*3 Insertion - Frameshift 15:50441463-50441464 + TCGA-FU-A3HZ-01 COSM4840956 c.2666A>C p.N889T Substitution - Missense 15:50495855-50495855 + YUKAT COSM5383471 c.162T>G p.R54R Substitution - coding silent 15:50441406-50441406 + B105-0-Tumor COSM1749198 c.2159C>G p.P720R Substitution - Missense 15:50490450-50490450 + TCGA-18-3410-01 COSM701089 c.631C>G p.Q211E Substitution - Missense 15:50465136-50465136 + SNUH_G76_S1 COSM4417633 c.1857T>C p.F619F Substitution - coding silent 15:50484328-50484328 + TCGA-BK-A13C-01 COSM962556 c.1065T>C p.S355S Substitution - coding silent 15:50477346-50477346 + PTC_231 COSM4770131 c.2391C>T p.N797N Substitution - coding silent 15:50492857-50492857 + TCGA-D1-A16J-01 COSM962548 c.145G>A p.E49K Substitution - Missense 15:50441389-50441389 + TCGA-BS-A0UF-01 COSM962558 c.1330C>T p.R444C Substitution - Missense 15:50481592-50481592 + ACINAR01 COSM404325 c.2353A>G p.T785A Substitution - Missense 15:50492819-50492819 + C467 COSM215607 c.2327T>C p.L776P Substitution - Missense 15:50492793-50492793 + 01-P459 COSM4442384 c.2144G>A p.R715H Substitution - Missense 15:50490435-50490435 + TCGA-A7-A3J1-01 COSM3816287 c.1993A>C p.T665P Substitution - Missense 15:50490284-50490284 + tumor_4177601 COSM3356739 c.2181A>G p.Q727Q Substitution - coding silent 15:50490472-50490472 + DLD1 COSM2216610 c.3119A>G p.Y1040C Substitution - Missense 15:50498676-50498676 + TCGA-B0-5080-01 COSM470768 c.3177C>G p.H1059Q Substitution - Missense 15:50498908-50498908 + LB647-SCLC COSM24333 c.160C>T p.R54C Substitution - Missense 15:50441404-50441404 + TCGA-AX-A05Z-01 COSM962562 c.1476G>T p.E492D Substitution - Missense 15:50481738-50481738 + 2367115 COSM4997303 c.2150A>G p.Y717C Substitution - Missense 15:50490441-50490441 + TCGA-BS-A0UV-01 COSM962560 c.1447C>T p.R483W Substitution - Missense 15:50481709-50481709 + 578 COSM3724121 c.1160C>G p.S387C Substitution - Missense 15:50477441-50477441 + TCGA-D3-A51R-06 COSM3501987 c.2473G>A p.E825K Substitution - Missense 15:50494095-50494095 + TCGA-18-3409-01 COSM701087 c.928C>T p.Q310* Substitution - Nonsense 15:50476927-50476927 + TCGA-DG-A2KH-01 COSM4770131 c.2391C>T p.N797N Substitution - coding silent 15:50492857-50492857 + TCGA-EK-A3GK-01 COSM2216563 c.475G>C p.D159H Substitution - Missense 15:50459139-50459139 + SJDES011-R COSM4578319 c.528G>C p.E176D Substitution - Missense 15:50462309-50462309 + TCGA-FD-A3NA-01 COSM1301202 c.2097G>C p.K699N Substitution - Missense 15:50490388-50490388 + 88 COSM5015296 c.2648A>G p.D883G Substitution - Missense 15:50494270-50494270 + GCT32 COSM2216596 c.2392G>C p.A798P Substitution - Missense 15:50492858-50492858 + RK280_C01 COSM4944443 c.850-8A>G p.? Unknown 15:50476841-50476841 + LUAD-LC15C COSM341718 c.1116G>T p.M372I Substitution - Missense 15:50477397-50477397 + TCGA-GM-A2D9-01 COSM3816289 c.2611G>C p.E871Q Substitution - Missense 15:50494233-50494233 + TCGA-BT-A2LB-01 COSM138063 c.1859G>A p.R620K Substitution - Missense 15:50484330-50484330 + TCGA-B5-A11E-01 COSM962552 c.414G>A p.R138R Substitution - coding silent 15:50459078-50459078 + PT45 COSM5927748 c.850-7T>C p.? Unknown 15:50476842-50476842 + TCGA-G9-6363-01 COSM404325 c.2353A>G p.T785A Substitution - Missense 15:50492819-50492819 + TCGA-BR-4292-01 COSM4055444 c.1726C>A p.P576T Substitution - Missense 15:50481988-50481988 + PT19_1 COSM5899688 c.2921A>G p.E974G Substitution - Missense 15:50497114-50497114 + TCGA-BR-6452-01 COSM4055443 c.875A>G p.N292S Substitution - Missense 15:50476874-50476874 + HN_62814 COSM130130 c.1075G>C p.D359H Substitution - Missense 15:50477356-50477356 + tumor_4177601 COSM3356740 c.2207T>C p.V736A Substitution - Missense 15:50490498-50490498 + CN-AML-NR-39-Dx COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-AA-3663-01 COSM1373372 c.2932A>C p.T978P Substitution - Missense 15:50497125-50497125 + 2552730 COSM1749198 c.2159C>G p.P720R Substitution - Missense 15:50490450-50490450 + XHDG41 COSM4770131 c.2391C>T p.N797N Substitution - coding silent 15:50492857-50492857 + ESCC_13 COSM5625147 c.1092G>C p.L364F Substitution - Missense 15:50477373-50477373 + HCC021T COSM5815622 c.309A>T p.E103D Substitution - Missense 15:50449459-50449459 + 2367115 COSM4997302 c.2138T>G p.L713R Substitution - Missense 15:50490429-50490429 + TCGA-C5-A1BI-01 COSM416905 c.2159C>A p.P720Q Substitution - Missense 15:50490450-50490450 + T3535 COSM4739951 c.454G>T p.G152C Substitution - Missense 15:50459118-50459118 + PT15_1 COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + TCGA-HC-8261-01 COSM4391848 c.3153T>C p.Y1051Y Substitution - coding silent 15:50498710-50498710 + TCGA-D3-A2JL-06 COSM3501982 c.226A>T p.R76* Substitution - Nonsense 15:50441470-50441470 + TCGA-CM-6171-01 COSM1373371 c.1918C>T p.R640* Substitution - Nonsense 15:50489828-50489828 + TCGA-AA-A010-01 COSM286412 c.1804-6T>G p.? Unknown 15:50484269-50484269 + 587376 COSM1232124 c.2231A>G p.N744S Substitution - Missense 15:50490522-50490522 + TCGA-A2-A1G4-01 COSM1478179 c.942T>C p.N314N Substitution - coding silent 15:50476941-50476941 + TCGA-P5-A5F0-01 COSM4420718 c.870G>C p.L290L Substitution - coding silent 15:50476869-50476869 + TCGA-BR-4361-01 COSM3356741 c.2366A>G p.N789S Substitution - Missense 15:50492832-50492832 + OSCC-GB_01270111 COSM5953920 c.2000G>A p.R667H Substitution - Missense 15:50490291-50490291 + TCGA-AX-A0J0-01 COSM962574 c.3103C>A p.L1035I Substitution - Missense 15:50498660-50498660 + 24-RS COSM1731978 c.2658+2_2658+3insAAGA p.? Unknown 15:50494282-50494283 + ccRCC-100 COSM1664928 c.1888A>G p.K630E Substitution - Missense 15:50484359-50484359 + 91 COSM3724120 c.1270A>C p.K424Q Substitution - Missense 15:50481532-50481532 + CN-AML-NR-39-Dx COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + 8057559 COSM3386923 c.199G>A p.V67M Substitution - Missense 15:50441443-50441443 + PT19_1 COSM5899689 c.2957G>A p.S986N Substitution - Missense 15:50497150-50497150 + B80 COSM1749199 c.2176A>G p.I726V Substitution - Missense 15:50490467-50490467 + BD57T COSM5510732 c.2730C>A p.A910A Substitution - coding silent 15:50495919-50495919 + LUAD-5V8LT COSM401552 c.2193G>T p.K731N Substitution - Missense 15:50490484-50490484 + PT20_1 COSM5900596 c.2933C>T p.T978I Substitution - Missense 15:50497126-50497126 + TCGA-E2-A1LK-01 COSM1478178 c.270T>G p.L90L Substitution - coding silent 15:50449420-50449420 + 2367114 COSM1731733 c.2153C>G p.S718C Substitution - Missense 15:50490444-50490444 + TCGA-G9-6338-01 COSM3672068 c.3181G>T p.G1061C Substitution - Missense 15:50498912-50498912 + TCGA-D1-A16Y-01 COSM962564 c.1919G>A p.R640Q Substitution - Missense 15:50489829-50489829 + TCGA-AZ-4315-01 COSM1373368 c.772C>T p.L258F Substitution - Missense 15:50471718-50471718 + C0031T COSM4150969 c.2658+6A>T p.? Unknown 15:50494286-50494286 + 14-RS COSM1731978 c.2658+2_2658+3insAAGA p.? Unknown 15:50494282-50494283 + CSCC-27-T COSM4568276 c.105T>G p.S35R Substitution - Missense 15:50441349-50441349 + TCGA-D3-A51T-06 COSM3501985 c.2107C>T p.P703S Substitution - Missense 15:50490398-50490398 + TCGA-AP-A051-01 COSM962554 c.1053G>A p.T351T Substitution - coding silent 15:50477334-50477334 + LUAD-B01145 COSM333263 c.2074A>C p.T692P Substitution - Missense 15:50490365-50490365 + TCGA-FW-A3R5-06 COSM3887108 c.2338C>T p.R780C Substitution - Missense 15:50492804-50492804 + TCGA-AN-A046-01 COSM3816285 c.1424A>C p.K475T Substitution - Missense 15:50481686-50481686 + TCGA-85-6560-01 COSM701086 c.2485G>C p.E829Q Substitution - Missense 15:50494107-50494107 + WSU-HN12 COSM4601047 c.547A>G p.I183V Substitution - Missense 15:50465052-50465052 + PT36 COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + CN-AML-CR-45-Dx COSM5424153 c.436G>A p.G146S Substitution - Missense 15:50459100-50459100 + TCGA-BT-A0S7-01 COSM416905 c.2159C>A p.P720Q Substitution - Missense 15:50490450-50490450 + S00935 COSM316425 c.621G>T p.M207I Substitution - Missense 15:50465126-50465126 + TCGA-FS-A1ZQ-06 COSM3501983 c.258C>T p.F86F Substitution - coding silent 15:50449408-50449408 + TCGA-B5-A11E-01 COSM962572 c.3066A>C p.Q1022H Substitution - Missense 15:50498623-50498623 + CN-AML-39-T COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-CG-4436-01 COSM4055446 c.3259G>C p.E1087Q Substitution - Missense 15:50498990-50498990 + PT20_1 COSM5899688 c.2921A>G p.E974G Substitution - Missense 15:50497114-50497114 + 2367111 COSM4997272 c.2151_2153delCTC p.S719delS Deletion - In frame 15:50490442-50490444 + PTC-28C COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-HM-A4S6-01 COSM4855020 c.317C>G p.S106C Substitution - Missense 15:50449467-50449467 + ASHPC_0016_Pa_P COSM701087 c.928C>T p.Q310* Substitution - Nonsense 15:50476927-50476927 + LUAD-S01346 COSM404325 c.2353A>G p.T785A Substitution - Missense 15:50492819-50492819 + BD236T COSM5519306 c.2420G>A p.R807Q Substitution - Missense 15:50492886-50492886 + TCGA-85-6561-01 COSM701088 c.885G>T p.L295F Substitution - Missense 15:50476884-50476884 + PT20_1 COSM5899689 c.2957G>A p.S986N Substitution - Missense 15:50497150-50497150 + TCGA-CA-6717-01 COSM1373363 c.98C>A p.T33N Substitution - Missense 15:50439171-50439171 + S00935 COSM316425 c.621G>T p.M207I Substitution - Missense 15:50465126-50465126 + TCGA-GV-A3JZ-01 COSM1301201 c.667G>A p.E223K Substitution - Missense 15:50465172-50465172 + TCGA-BP-4967-01 COSM470767 c.708A>G p.E236E Substitution - coding silent 15:50471654-50471654 + MB_Exm23 COSM215607 c.2327T>C p.L776P Substitution - Missense 15:50492793-50492793 + TCGA-FS-A1ZP-06 COSM3887109 c.2535C>T p.I845I Substitution - coding silent 15:50494157-50494157 + TCGA-BS-A0UJ-01 COSM962568 c.2814A>G p.T938T Substitution - coding silent 15:50496003-50496003 + CHC361TA COSM2216600 c.2531A>G p.Y844C Substitution - Missense 15:50494153-50494153 + T1743 COSM4739952 c.968G>A p.R323H Substitution - Missense 15:50476967-50476967 + TCGA-OL-A66K-01 COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 + 2476_PT COSM2216573 c.824G>A p.R275Q Substitution - Missense 15:50471770-50471770 + PT31 COSM5906967 c.2225G>A p.R742Q Substitution - Missense 15:50490516-50490516 + 1946219 COSM1578452 c.1624_1625insG p.A542fs*15 Insertion - Frameshift 15:50481886-50481887 + tumor_4188900 COSM3356741 c.2366A>G p.N789S Substitution - Missense 15:50492832-50492832 + PCSI_0509_Pa_P_526 COSM4962027 c.1972-4T>A p.? Unknown 15:50490259-50490259 + 2367113 COSM4997287 c.2152T>C p.S718P Substitution - Missense 15:50490443-50490443 + TCGA-ER-A19F-06 COSM3887110 c.3293C>T p.S1098F Substitution - Missense 15:50499024-50499024 + TCGA-D5-6540-01 COSM1373370 c.1495C>T p.Q499* Substitution - Nonsense 15:50481757-50481757 + TCGA-IR-A3LI-01 COSM4846033 c.1845G>A p.R615R Substitution - coding silent 15:50484316-50484316 + SNU-175 COSM2216600 c.2531A>G p.Y844C Substitution - Missense 15:50494153-50494153 + T3091 COSM2216582 c.1390C>T p.R464C Substitution - Missense 15:50481652-50481652 + PT46 COSM5929627 c.2347G>T p.G783* Substitution - Nonsense 15:50492813-50492813 + CSCC-16-T COSM4510564 c.841C>T p.L281F Substitution - Missense 15:50471787-50471787 + TCGA-AZ-4615-01 COSM5139669 c.2985delA p.K997fs*2 Deletion - Frameshift 15:50497178-50497178 + TCGA-EK-A3GJ-01 COSM4852443 c.2502G>T p.M834I Substitution - Missense 15:50494124-50494124 + TCGA-GN-A26C-01 COSM3501986 c.2147C>T p.S716F Substitution - Missense 15:50490438-50490438 + PTC_27 COSM2216596 c.2392G>C p.A798P Substitution - Missense 15:50492858-50492858 + tumor_4177601 COSM3356737 c.2009A>G p.H670R Substitution - Missense 15:50490300-50490300 + SNU-C4 COSM4652607 c.1148C>T p.P383L Substitution - Missense 15:50477429-50477429 + U373 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-BS-A0UV-01 COSM962566 c.2686G>T p.E896* Substitution - Nonsense 15:50495875-50495875 + PT46 COSM5929628 c.2348G>A p.G783E Substitution - Missense 15:50492814-50492814 + TCGA-H4-A2HQ-01 COSM1301203 c.2281C>G p.Q761E Substitution - Missense 15:50492747-50492747 + 2552728 COSM4997287 c.2152T>C p.S718P Substitution - Missense 15:50490443-50490443 + HN_62857_2 COSM130131 c.2206G>A p.V736I Substitution - Missense 15:50490497-50490497 + TCGA-D3-A2JO-06 COSM3501985 c.2107C>T p.P703S Substitution - Missense 15:50490398-50490398 + DLD1 COSM4623125 c.844T>C p.F282L Substitution - Missense 15:50471790-50471790 + CSCC-31-T COSM4536951 c.2364G>A p.M788I Substitution - Missense 15:50492830-50492830 + Gp2D COSM4627322 c.2051C>T p.A684V Substitution - Missense 15:50490342-50490342 + SWE-21 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + LUAD-YINHD COSM349048 c.1181T>A p.I394K Substitution - Missense 15:50477462-50477462 + ccRCC-28 COSM1664929 c.2056T>G p.S686A Substitution - Missense 15:50490347-50490347 + TCGA-ED-A459-01 COSM4935565 c.2122A>G p.R708G Substitution - Missense 15:50490413-50490413 + C547 COSM4442384 c.2144G>A p.R715H Substitution - Missense 15:50490435-50490435 + PDA_023 COSM4999189 c.1084A>G p.I362V Substitution - Missense 15:50477365-50477365 + TCGA-HU-A4H8-01 COSM4055445 c.2143C>T p.R715C Substitution - Missense 15:50490434-50490434 + 2324293 COSM1179083 c.2292C>A p.N764K Substitution - Missense 15:50492758-50492758 + TCGA-E2-A10B-01 COSM434007 c.2158C>G p.P720A Substitution - Missense 15:50490449-50490449 + TCGA-EE-A2MS-06 COSM3501984 c.1955C>T p.P652L Substitution - Missense 15:50489865-50489865 + TCGA-BS-A0UV-01 COSM962564 c.1919G>A p.R640Q Substitution - Missense 15:50489829-50489829 + CN-AML-39-T COSM3816288 c.2287C>T p.R763W Substitution - Missense 15:50492753-50492753 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.443731 15q21.2 603158

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.Q324R c.971A>G 15 50769167 LUAD A G Synonymous p.E236E c.708A>G 15 50763851 RCCC A T Missense p.R112S c.336A>T 15 50751197 UCEC A T Missense p.T637S c.1909A>T 15 50782016 ESCA A T Nonsense p.R76* c.226A>T 15 50733667 CM C A Missense p.P576T c.1726C>A 15 50774185 STAD C A Missense p.P720Q c.2159C>A 15 50782647 BLCA C G Missense p.H1059Q c.3177C>G 15 50791105 RCCC C G Missense p.H881D c.2641C>G 15 50786460 CM C G Missense p.P720A c.2158C>G 15 50782646 BRCA C G Missense p.Q211E c.631C>G 15 50757333 LUSC C G Missense p.Q761E c.2281C>G 15 50784944 BLCA C G Missense p.S1092C c.3275C>G 15 50791203 LUAD C G Missense p.S387C c.1160C>G 15 50769638 HNSC C G Synonymous p.A59A c.177C>G 15 50733618 ESCA C T IntronicSNV . c.2896-39C>T 15 50789247 CM C T IntronicSNV . c.686+1788C>T 15 50759176 CM C T Missense p.L11F c.31C>T 15 50731301 CM C T Missense p.P652L c.1955C>T 15 50782062 CM C T Missense p.P703S c.2107C>T 15 50782595 CM C T Missense p.R409C c.1225C>T 15 50773684 CM C T Missense p.S1098F c.3293C>T 15 50791221 CM C T Missense p.S716F c.2147C>T 15 50782635 CM C T Missense p.S772F c.2315C>T 15 50784978 CM C T Missense p.T193M c.578C>T 15 50757280 OV C T Nonsense p.R1112* c.3334C>T 15 50791262 HNSC C T Synonymous p.F79F c.237C>T 15 50733678 GBM C T Synonymous p.F86F c.258C>T 15 50741605 CM C T Synonymous p.I647I c.1941C>T 15 50782048 CM C T Synonymous p.I845I c.2535C>T 15 50786354 CM G A Missense p.E223K c.667G>A 15 50757369 BLCA G A Missense p.E511K c.1531G>A 15 50773990 CM G A Missense p.E57K c.169G>A 15 50733610 NB G A Missense p.G840E c.2519G>A 15 50786338 HNSC G A Missense p.R620K c.1859G>A 15 50776527 BLCA G A Missense p.R640Q c.1919G>A 15 50782026 UCEC G A Missense p.V736I c.2206G>A 15 50782694 HNSC G A Nonsense p.W1001* c.3003G>A 15 50789393 LUAD G A Synonymous p.E56E c.168G>A 15 50733609 LUSC G A Synonymous p.K915K c.2745G>A 15 50788131 MM G A Synonymous p.Q324Q c.972G>A 15 50769168 HNSC G C Missense p.D359H c.1075G>C 15 50769553 HNSC G C Missense p.D570H c.1708G>C 15 50774167 HNSC G C Missense p.E1087Q c.3259G>C 15 50791187 STAD G C Missense p.E829Q c.2485G>C 15 50786304 LUSC G C Missense p.K699N c.2097G>C 15 50782585 BLCA G C Synonymous p.L277L c.831G>C 15 50763974 HNSC G C Synonymous p.R890R c.2670G>C 15 50788056 HNSC G T Missense p.A907S c.2719G>T 15 50788105 PRAD G T Missense p.E728D c.2184G>T 15 50782672 STAD G T Missense p.G1061C c.3181G>T 15 50791109 PRAD G T Missense p.G91V c.272G>T 15 50741619 LUAD G T Missense p.L295F c.885G>T 15 50769081 LUSC G T Missense p.M207I c.621G>T 15 50757323 SCLC G T Missense p.R409L c.1226G>T 15 50773685 HNSC T A IntronicSNV . c.2447+18T>A 15 50785128 ESCA T C IntronicSNV . c.2448-33T>C 15 50786234 NSCLC T C Missense p.L776P c.2327T>C 15 50784990 MB T C Synonymous p.F904F c.2712T>C 15 50788098 GBM T C Synonymous p.N314N c.942T>C 15 50769138 BRCA T C Synonymous p.S355S c.1065T>C 15 50769543 UCEC T C Synonymous p.Y1051Y c.3153T>C 15 50790907 PRAD T G 3-UTRSNV . c.3354+479T>G 15 50791761 HC T G Missense p.Y60D c.178T>G 15 50733619 HNSC T G Synonymous p.L90L c.270T>G 15 50741617 BRCA T G Synonymous p.S387S c.1161T>G 15 50769639 LUAD