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 6 149983114 149983114 + Nonsense_Mutation SNP C C T TCGA-K4-A5RI-01A-11D-A289-08 TCGA-K4-A5RI-10A-01D-A289-08 g.chr6:149983114C>T c.3144G>A c.(3142-3144)tgG>tgA p.W1048* BLCA 6 150001017 150001017 + Missense_Mutation SNP G G C TCGA-CF-A3MG-01A-11D-A20D-08 TCGA-CF-A3MG-10A-01D-A20D-08 g.chr6:150001017G>C c.2587C>G c.(2587-2589)Cag>Gag p.Q863E BLCA 6 150001083 150001083 + Missense_Mutation SNP G G A TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr6:150001083G>A c.2521C>T c.(2521-2523)Cat>Tat p.H841Y BLCA 6 150001152 150001152 + Missense_Mutation SNP T T C TCGA-2F-A9KW-01A-11D-A38G-08 TCGA-2F-A9KW-10A-01D-A38J-08 g.chr6:150001152T>C c.2452A>G c.(2452-2454)Agt>Ggt p.S818G BLCA 6 150001312 150001312 + Nonsense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr6:150001312C>T c.2292G>A c.(2290-2292)tgG>tgA p.W764* BLCA 6 150001317 150001317 + Missense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr6:150001317C>T c.2287G>A c.(2287-2289)Gaa>Aaa p.E763K BLCA 6 150001347 150001347 + Missense_Mutation SNP C C G TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr6:150001347C>G c.2257G>C c.(2257-2259)Gag>Cag p.E753Q BLCA 6 150001347 150001347 + Missense_Mutation SNP C C G TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr6:150001347C>G c.2257G>C c.(2257-2259)Gag>Cag p.E753Q BLCA 6 150001523 150001523 + Missense_Mutation SNP C C T TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr6:150001523C>T c.2081G>A c.(2080-2082)cGt>cAt p.R694H BLCA 6 150004798 150004798 + Missense_Mutation SNP G G A TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr6:150004798G>A c.1427C>T c.(1426-1428)tCt>tTt p.S476F BLCA 6 150004840 150004840 + Nonsense_Mutation SNP G G C TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr6:150004840G>C c.1385C>G c.(1384-1386)tCa>tGa p.S462* BLCA 6 150004847 150004847 + Missense_Mutation SNP C C T TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr6:150004847C>T c.1378G>A c.(1378-1380)Gtg>Atg p.V460M BLCA 6 150004897 150004897 + Nonsense_Mutation SNP G G C TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr6:150004897G>C c.1328C>G c.(1327-1329)tCa>tGa p.S443* BLCA 6 150004901 150004901 + Missense_Mutation SNP G G T TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr6:150004901G>T c.1324C>A c.(1324-1326)Cag>Aag p.Q442K BLCA 6 150005006 150005006 + Nonsense_Mutation SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr6:150005006G>A c.1219C>T c.(1219-1221)Cag>Tag p.Q407* BLCA 6 150005065 150005065 + Missense_Mutation SNP G G A TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr6:150005065G>A c.1160C>T c.(1159-1161)tCt>tTt p.S387F BLCA 6 150005093 150005093 + Silent SNP G G A TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr6:150005093G>A c.1132C>T c.(1132-1134)Ctg>Ttg p.L378L BLCA 6 150005361 150005361 + Missense_Mutation SNP G G C TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr6:150005361G>C c.864C>G c.(862-864)atC>atG p.I288M BLCA 6 150005575 150005575 + Missense_Mutation SNP C C T TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr6:150005575C>T c.650G>A c.(649-651)gGa>gAa p.G217E BLCA 6 150005691 150005691 + Nonsense_Mutation SNP C C T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr6:150005691C>T c.534G>A c.(532-534)tgG>tgA p.W178* BLCA 6 150023112 150023112 + Missense_Mutation SNP C C T TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr6:150023112C>T c.151G>A c.(151-153)Gag>Aag p.E51K BLCA 6 150023160 150023160 + Missense_Mutation SNP G G A TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr6:150023160G>A c.103C>T c.(103-105)Cgg>Tgg p.R35W BLCA 6 150023254 150023254 + Silent SNP C C T TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr6:150023254C>T c.9G>A c.(7-9)agG>agA p.R3R BRCA 6 149983176 149983176 + Missense_Mutation SNP G G C TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr6:149983176G>C c.3082C>G c.(3082-3084)Cct>Gct p.P1028A BRCA 6 149983263 149983263 + Missense_Mutation SNP T T C TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:149983263T>C c.2995A>G c.(2995-2997)Aat>Gat p.N999D BRCA 6 150001092 150001092 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:150001092G>C c.2512C>G c.(2512-2514)Cgt>Ggt p.R838G BRCA 6 150005196 150005196 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:150005196C>T c.1029G>A c.(1027-1029)ggG>ggA p.G343G BRCA 6 150023155 150023155 + Missense_Mutation SNP T T A TCGA-C8-A26V-01A-11D-A16D-09 TCGA-C8-A26V-10A-01D-A16D-09 g.chr6:150023155T>A c.108A>T c.(106-108)gaA>gaT p.E36D CESC 6 149983239 149983239 + Missense_Mutation SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr6:149983239G>A c.3019C>T c.(3019-3021)Cat>Tat p.H1007Y CESC 6 149997435 149997435 + Silent SNP A A C TCGA-R2-A69V-01A-11D-A32I-09 TCGA-R2-A69V-10A-01D-A32I-09 g.chr6:149997435A>C c.2844T>G c.(2842-2844)ccT>ccG p.P948P CESC 6 149997469 149997469 + Missense_Mutation SNP C C A TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chr6:149997469C>A c.2810G>T c.(2809-2811)gGt>gTt p.G937V CESC 6 149997697 149997697 + Nonsense_Mutation SNP G G A TCGA-EX-A69M-01A-11D-A32I-09 TCGA-EX-A69M-10A-01D-A32I-09 g.chr6:149997697G>A c.2770C>T c.(2770-2772)Cga>Tga p.R924* CESC 6 150001486 150001486 + Silent SNP C C A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr6:150001486C>A c.2118G>T c.(2116-2118)gtG>gtT p.V706V CESC 6 150001559 150001559 + Missense_Mutation SNP C C G TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr6:150001559C>G c.2045G>C c.(2044-2046)aGa>aCa p.R682T CESC 6 150004568 150004568 + Missense_Mutation SNP G G C TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr6:150004568G>C c.1657C>G c.(1657-1659)Caa>Gaa p.Q553E CESC 6 150004621 150004621 + Missense_Mutation SNP C C T TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr6:150004621C>T c.1604G>A c.(1603-1605)gGa>gAa p.G535E CESC 6 150005408 150005408 + Nonsense_Mutation SNP G G A TCGA-EA-A6QX-01A-12D-A33O-09 TCGA-EA-A6QX-10B-01D-A33O-09 g.chr6:150005408G>A c.817C>T c.(817-819)Caa>Taa p.Q273* CESC 6 150005474 150005474 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr6:150005474G>C c.751C>G c.(751-753)Cca>Gca p.P251A CESC 6 150005552 150005552 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr6:150005552G>C c.673C>G c.(673-675)Caa>Gaa p.Q225E CESC 6 150005605 150005605 + Nonsense_Mutation SNP G G C TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr6:150005605G>C c.620C>G c.(619-621)tCa>tGa p.S207* CESC 6 150016267 150016267 + Nonsense_Mutation SNP G G A TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chr6:150016267G>A c.439C>T c.(439-441)Cga>Tga p.R147* COAD 6 149982976 149982976 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:149982976C>T c.3282G>A c.(3280-3282)ccG>ccA p.P1094P COAD 6 149983088 149983088 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:149983088A>G c.3170T>C c.(3169-3171)gTa>gCa p.V1057A COAD 6 149983289 149983289 + Missense_Mutation SNP C C T TCGA-AA-A02H-01A-01W-A00E-09 TCGA-AA-A02H-10A-01W-A00E-09 g.chr6:149983289C>T c.2969G>A c.(2968-2970)cGa>cAa p.R990Q COAD 6 149997822 149997822 + Missense_Mutation SNP G G T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr6:149997822G>T c.2645C>A c.(2644-2646)cCc>cAc p.P882H COAD 6 150001188 150001188 + Nonsense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:150001188G>A c.2416C>T c.(2416-2418)Cga>Tga p.R806* COAD 6 150001190 150001190 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr6:150001190G>A c.2414C>T c.(2413-2415)gCa>gTa p.A805V COAD 6 150001235 150001235 + Missense_Mutation SNP A A G TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr6:150001235A>G c.2369T>C c.(2368-2370)aTg>aCg p.M790T COAD 6 150001373 150001373 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:150001373C>T c.2231G>A c.(2230-2232)cGa>cAa p.R744Q COAD 6 150001448 150001448 + Missense_Mutation SNP A A G TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:150001448A>G c.2156T>C c.(2155-2157)gTc>gCc p.V719A COAD 6 150001448 150001448 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr6:150001448A>G c.2156T>C c.(2155-2157)gTc>gCc p.V719A COAD 6 150001474 150001474 + Silent SNP T T C TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr6:150001474T>C c.2130A>G c.(2128-2130)acA>acG p.T710T COAD 6 150001494 150001494 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:150001494T>C c.2110A>G c.(2110-2112)Atg>Gtg p.M704V COAD 6 150001540 150001540 + Frame_Shift_Del DEL T T - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:150001540delT c.2064delA c.(2062-2064)aaafs p.K688fs COAD 6 150004239 150004239 + Frame_Shift_Del DEL T T - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:150004239delT c.1986delA c.(1984-1986)aaafs p.K662fs COAD 6 150004302 150004302 + Missense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:150004302G>T c.1923C>A c.(1921-1923)ttC>ttA p.F641L COAD 6 150004719 150004719 + Silent SNP A A G TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COAD 6 150004719 150004719 + Silent SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COAD 6 150004719 150004719 + Silent SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C COAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C COAD 6 150005219 150005219 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:150005219T>C c.1006A>G c.(1006-1008)Agc>Ggc p.S336G COAD 6 150005323 150005323 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:150005323G>T c.902C>A c.(901-903)cCt>cAt p.P301H COAD 6 150005460 150005460 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr6:150005460A>G c.765T>C c.(763-765)acT>acC p.T255T COAD 6 150005462 150005462 + Missense_Mutation SNP T T C TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr6:150005462T>C c.763A>G c.(763-765)Act>Gct p.T255A COAD 6 150005462 150005462 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr6:150005462T>C c.763A>G c.(763-765)Act>Gct p.T255A COAD 6 150005469 150005469 + Silent SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COAD 6 150005469 150005469 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COAD 6 150005469 150005469 + Silent SNP T T C TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COAD 6 150005471 150005471 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:150005471T>C c.754A>G c.(754-756)Aga>Gga p.R252G COAD 6 150005471 150005471 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:150005471T>C c.754A>G c.(754-756)Aga>Gga p.R252G COAD 6 150023084 150023084 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:150023084T>C c.179A>G c.(178-180)gAa>gGa p.E60G COAD 6 150023094 150023094 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:150023094T>C c.169A>G c.(169-171)Atg>Gtg p.M57V COADREAD 6 149982976 149982976 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:149982976C>T c.3282G>A c.(3280-3282)ccG>ccA p.P1094P COADREAD 6 149983088 149983088 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:149983088A>G c.3170T>C c.(3169-3171)gTa>gCa p.V1057A COADREAD 6 149983274 149983274 + Missense_Mutation SNP C C T TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr6:149983274C>T c.2984G>A c.(2983-2985)cGc>cAc p.R995H COADREAD 6 149983289 149983289 + Missense_Mutation SNP C C T TCGA-AA-A02H-01A-01W-A00E-09 TCGA-AA-A02H-10A-01W-A00E-09 g.chr6:149983289C>T c.2969G>A c.(2968-2970)cGa>cAa p.R990Q COADREAD 6 149997822 149997822 + Missense_Mutation SNP G G T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr6:149997822G>T c.2645C>A c.(2644-2646)cCc>cAc p.P882H COADREAD 6 150001188 150001188 + Nonsense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:150001188G>A c.2416C>T c.(2416-2418)Cga>Tga p.R806* COADREAD 6 150001190 150001190 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr6:150001190G>A c.2414C>T c.(2413-2415)gCa>gTa p.A805V COADREAD 6 150001235 150001235 + Missense_Mutation SNP A A G TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr6:150001235A>G c.2369T>C c.(2368-2370)aTg>aCg p.M790T COADREAD 6 150001373 150001373 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:150001373C>T c.2231G>A c.(2230-2232)cGa>cAa p.R744Q COADREAD 6 150001395 150001395 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:150001395G>A c.2209C>T c.(2209-2211)Cga>Tga p.R737* COADREAD 6 150001448 150001448 + Missense_Mutation SNP A A G TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:150001448A>G c.2156T>C c.(2155-2157)gTc>gCc p.V719A COADREAD 6 150001448 150001448 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr6:150001448A>G c.2156T>C c.(2155-2157)gTc>gCc p.V719A COADREAD 6 150001474 150001474 + Silent SNP T T C TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr6:150001474T>C c.2130A>G c.(2128-2130)acA>acG p.T710T COADREAD 6 150001494 150001494 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:150001494T>C c.2110A>G c.(2110-2112)Atg>Gtg p.M704V COADREAD 6 150001540 150001540 + Frame_Shift_Del DEL T T - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:150001540delT c.2064delA c.(2062-2064)aaafs p.K688fs COADREAD 6 150004239 150004239 + Frame_Shift_Del DEL T T - TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr6:150004239delT c.1986delA c.(1984-1986)aaafs p.K662fs COADREAD 6 150004302 150004302 + Missense_Mutation SNP G G T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr6:150004302G>T c.1923C>A c.(1921-1923)ttC>ttA p.F641L COADREAD 6 150004719 150004719 + Silent SNP A A G TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COADREAD 6 150004719 150004719 + Silent SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COADREAD 6 150004719 150004719 + Silent SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr6:150004719A>G c.1506T>C c.(1504-1506)cgT>cgC p.R502R COADREAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C COADREAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C COADREAD 6 150005219 150005219 + Missense_Mutation SNP T T C TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:150005219T>C c.1006A>G c.(1006-1008)Agc>Ggc p.S336G COADREAD 6 150005323 150005323 + Missense_Mutation SNP G G T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr6:150005323G>T c.902C>A c.(901-903)cCt>cAt p.P301H COADREAD 6 150005395 150005395 + Missense_Mutation SNP T T C TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr6:150005395T>C c.830A>G c.(829-831)tAt>tGt p.Y277C COADREAD 6 150005460 150005460 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr6:150005460A>G c.765T>C c.(763-765)acT>acC p.T255T COADREAD 6 150005462 150005462 + Missense_Mutation SNP T T C TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr6:150005462T>C c.763A>G c.(763-765)Act>Gct p.T255A COADREAD 6 150005462 150005462 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr6:150005462T>C c.763A>G c.(763-765)Act>Gct p.T255A COADREAD 6 150005469 150005469 + Silent SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COADREAD 6 150005469 150005469 + Silent SNP T T C TCGA-D5-6534-01A-21D-1924-10 TCGA-D5-6534-10A-01D-1924-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COADREAD 6 150005469 150005469 + Silent SNP T T C TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr6:150005469T>C c.756A>G c.(754-756)agA>agG p.R252R COADREAD 6 150005471 150005471 + Missense_Mutation SNP T T C TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr6:150005471T>C c.754A>G c.(754-756)Aga>Gga p.R252G COADREAD 6 150005471 150005471 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:150005471T>C c.754A>G c.(754-756)Aga>Gga p.R252G COADREAD 6 150023084 150023084 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:150023084T>C c.179A>G c.(178-180)gAa>gGa p.E60G COADREAD 6 150023094 150023094 + Missense_Mutation SNP T T C TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:150023094T>C c.169A>G c.(169-171)Atg>Gtg p.M57V ESCA 6 149983001 149983001 + Missense_Mutation SNP T T A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr6:149983001T>A c.3257A>T c.(3256-3258)gAc>gTc p.D1086V ESCA 6 149997781 149997781 + Silent SNP G G T TCGA-XP-A8T7-01A-11D-A36J-09 TCGA-XP-A8T7-10A-01D-A36M-09 g.chr6:149997781G>T c.2686C>A c.(2686-2688)Cgg>Agg p.R896R ESCA 6 150005070 150005070 + Missense_Mutation SNP G G T TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr6:150005070G>T c.1155C>A c.(1153-1155)agC>agA p.S385R ESCA 6 150005477 150005477 + Missense_Mutation SNP G G T TCGA-XP-A8T6-01A-11D-A36J-09 TCGA-XP-A8T6-10A-01D-A36M-09 g.chr6:150005477G>T c.748C>A c.(748-750)Cct>Act p.P250T GBMLGG 6 150001374 150001376 + In_Frame_Del DEL GAA GAA - TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr6:150001374_150001376delGAA c.2228_2230delTTC c.(2227-2232)cttcga>cga p.L743del GBMLGG 6 150005294 150005294 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:150005294T>C c.931A>G c.(931-933)Aat>Gat p.N311D GBMLGG 6 150005421 150005421 + Nonsense_Mutation SNP C C T TCGA-WY-A85D-01A-11D-A36O-08 TCGA-WY-A85D-10A-01D-A367-08 g.chr6:150005421C>T c.804G>A c.(802-804)tgG>tgA p.W268* GBMLGG 6 150005515 150005515 + Frame_Shift_Del DEL G G - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr6:150005515delG c.710delC c.(709-711)ccafs p.P240fs HNSC 6 149983190 149983190 + Missense_Mutation SNP G G C TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr6:149983190G>C c.3068C>G c.(3067-3069)tCt>tGt p.S1023C HNSC 6 149997417 149997417 + Silent SNP T T A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr6:149997417T>A c.2862A>T c.(2860-2862)acA>acT p.T954T HNSC 6 150001095 150001095 + Missense_Mutation SNP C C G TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr6:150001095C>G c.2509G>C c.(2509-2511)Gat>Cat p.D837H HNSC 6 150001304 150001304 + Missense_Mutation SNP C C A TCGA-D6-6517-01A-11D-1870-08 TCGA-D6-6517-10A-01D-1870-08 g.chr6:150001304C>A c.2300G>T c.(2299-2301)cGt>cTt p.R767L HNSC 6 150004897 150004897 + Nonsense_Mutation SNP G G C TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr6:150004897G>C c.1328C>G c.(1327-1329)tCa>tGa p.S443* HNSC 6 150005093 150005093 + Silent SNP G G A TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr6:150005093G>A c.1132C>T c.(1132-1134)Ctg>Ttg p.L378L HNSC 6 150005102 150005102 + Missense_Mutation SNP G G A TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr6:150005102G>A c.1123C>T c.(1123-1125)Cca>Tca p.P375S HNSC 6 150005544 150005544 + Missense_Mutation SNP G G C TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr6:150005544G>C c.681C>G c.(679-681)caC>caG p.H227Q HNSC 6 150005651 150005651 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr6:150005651G>A c.574C>T c.(574-576)Ccg>Tcg p.P192S HNSC 6 150005729 150005729 + Splice_Site SNP C C T TCGA-CQ-5324-01A-01D-1683-08 TCGA-CQ-5324-10A-01D-1683-08 g.chr6:150005729C>T c.e4-1 KIPAN 6 149997827 149997827 + Silent SNP C C G TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr6:149997827C>G c.2640G>C c.(2638-2640)ggG>ggC p.G880G KIPAN 6 150001249 150001249 + Silent SNP A A G TCGA-BP-4807-01A-01D-1373-10 TCGA-BP-4807-11A-01D-1373-10 g.chr6:150001249A>G c.2355T>C c.(2353-2355)atT>atC p.I785I KIPAN 6 150004253 150004253 + Missense_Mutation SNP G G C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr6:150004253G>C c.1972C>G c.(1972-1974)Cta>Gta p.L658V KIPAN 6 150004564 150004564 + Missense_Mutation SNP C C T TCGA-BP-4989-01A-01D-1462-08 TCGA-BP-4989-11A-01D-1462-08 g.chr6:150004564C>T c.1661G>A c.(1660-1662)gGa>gAa p.G554E KIPAN 6 150005370 150005370 + Silent SNP G G T TCGA-BQ-7048-01A-11D-1961-08 TCGA-BQ-7048-11A-01D-1961-08 g.chr6:150005370G>T c.855C>A c.(853-855)atC>atA p.I285I KIPAN 6 150023180 150023180 + Missense_Mutation SNP C C T TCGA-B0-5710-01A-11D-1669-08 TCGA-B0-5710-11A-01D-1669-08 g.chr6:150023180C>T c.83G>A c.(82-84)cGg>cAg p.R28Q KIRC 6 150001249 150001249 + Silent SNP A A G TCGA-BP-4807-01A-01D-1373-10 TCGA-BP-4807-11A-01D-1373-10 g.chr6:150001249A>G c.2355T>C c.(2353-2355)atT>atC p.I785I KIRC 6 150004564 150004564 + Missense_Mutation SNP C C T TCGA-BP-4989-01A-01D-1462-08 TCGA-BP-4989-11A-01D-1462-08 g.chr6:150004564C>T c.1661G>A c.(1660-1662)gGa>gAa p.G554E KIRC 6 150023180 150023180 + Missense_Mutation SNP C C T TCGA-B0-5710-01A-11D-1669-08 TCGA-B0-5710-11A-01D-1669-08 g.chr6:150023180C>T c.83G>A c.(82-84)cGg>cAg p.R28Q KIRP 6 149997827 149997827 + Silent SNP C C G TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr6:149997827C>G c.2640G>C c.(2638-2640)ggG>ggC p.G880G KIRP 6 150004253 150004253 + Missense_Mutation SNP G G C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr6:150004253G>C c.1972C>G c.(1972-1974)Cta>Gta p.L658V KIRP 6 150005370 150005370 + Silent SNP G G T TCGA-BQ-7048-01A-11D-1961-08 TCGA-BQ-7048-11A-01D-1961-08 g.chr6:150005370G>T c.855C>A c.(853-855)atC>atA p.I285I LGG 6 150001374 150001376 + In_Frame_Del DEL GAA GAA - TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr6:150001374_150001376delGAA c.2228_2230delTTC c.(2227-2232)cttcga>cga p.L743del LGG 6 150005294 150005294 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:150005294T>C c.931A>G c.(931-933)Aat>Gat p.N311D LGG 6 150005421 150005421 + Nonsense_Mutation SNP C C T TCGA-WY-A85D-01A-11D-A36O-08 TCGA-WY-A85D-10A-01D-A367-08 g.chr6:150005421C>T c.804G>A c.(802-804)tgG>tgA p.W268* LGG 6 150005515 150005515 + Frame_Shift_Del DEL G G - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr6:150005515delG c.710delC c.(709-711)ccafs p.P240fs LIHC 6 149997708 149997708 + Missense_Mutation SNP T T C TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr6:149997708T>C c.2759A>G c.(2758-2760)gAa>gGa p.E920G LIHC 6 149997737 149997737 + Silent SNP C C T TCGA-G3-A5SI-01A-31D-A27I-10 TCGA-G3-A5SI-10A-01D-A27I-10 g.chr6:149997737C>T c.2730G>A c.(2728-2730)ttG>ttA p.L910L LIHC 6 149997738 149997738 + Missense_Mutation SNP A A G TCGA-DD-AAEG-01A-11D-A38X-10 TCGA-DD-AAEG-10A-01D-A38X-10 g.chr6:149997738A>G c.2729T>C c.(2728-2730)tTg>tCg p.L910S LIHC 6 150001056 150001058 + In_Frame_Del DEL AGA AGA - TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr6:150001056_150001058delAGA c.2546_2548delTCT c.(2545-2550)ctctgc>cgc p.849_850LC>R LIHC 6 150001298 150001298 + Missense_Mutation SNP T T C TCGA-DD-AAEE-01A-11D-A40R-10 TCGA-DD-AAEE-10A-01D-A40U-10 g.chr6:150001298T>C c.2306A>G c.(2305-2307)tAt>tGt p.Y769C LIHC 6 150001577 150001577 + Missense_Mutation SNP T T C TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr6:150001577T>C c.2027A>G c.(2026-2028)gAt>gGt p.D676G LIHC 6 150004716 150004717 + De_novo_Start_OutOfFrame INS - - ACACGCATACTTTTCACAGGCTGTTGAATAGG TCGA-RC-A6M6-01A-11D-A32G-10 TCGA-RC-A6M6-10A-01D-A32G-10 g.chr6:150004716_150004717insACACGCATACTTTTCACAGGCTGTTGAATAGG LIHC 6 150005471 150005471 + Nonsense_Mutation SNP T T A TCGA-RC-A6M4-01A-11D-A32G-10 TCGA-RC-A6M4-10A-01D-A32G-10 g.chr6:150005471T>A c.754A>T c.(754-756)Aga>Tga p.R252* LUAD 6 149982925 149982925 + Silent SNP C C A TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr6:149982925C>A c.3333G>T c.(3331-3333)tcG>tcT p.S1111S LUAD 6 149983170 149983170 + Missense_Mutation SNP T T C TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chr6:149983170T>C c.3088A>G c.(3088-3090)Atc>Gtc p.I1030V LUAD 6 149983376 149983376 + Splice_Site SNP T T A TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr6:149983376T>A c.e8-2 LUAD 6 150001145 150001145 + Missense_Mutation SNP T T C TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr6:150001145T>C c.2459A>G c.(2458-2460)cAt>cGt p.H820R LUAD 6 150001196 150001196 + Missense_Mutation SNP C C G TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr6:150001196C>G c.2408G>C c.(2407-2409)aGt>aCt p.S803T LUAD 6 150001244 150001244 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr6:150001244C>A c.2360G>T c.(2359-2361)gGg>gTg p.G787V LUAD 6 150001319 150001319 + Missense_Mutation SNP T T C TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr6:150001319T>C c.2285A>G c.(2284-2286)aAt>aGt p.N762S LUAD 6 150001332 150001332 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr6:150001332C>A c.2272G>T c.(2272-2274)Gct>Tct p.A758S LUAD 6 150001333 150001333 + Silent SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr6:150001333C>A c.2271G>T c.(2269-2271)ctG>ctT p.L757L LUAD 6 150001373 150001373 + Missense_Mutation SNP C C A TCGA-75-5147-01A-01D-1625-08 TCGA-75-5147-10A-01D-1625-08 g.chr6:150001373C>A c.2231G>T c.(2230-2232)cGa>cTa p.R744L LUAD 6 150004668 150004668 + Missense_Mutation SNP C C G TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr6:150004668C>G c.1557G>C c.(1555-1557)tgG>tgC p.W519C LUAD 6 150004813 150004813 + Missense_Mutation SNP T T C TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr6:150004813T>C c.1412A>G c.(1411-1413)aAt>aGt p.N471S LUAD 6 150004837 150004837 + Missense_Mutation SNP T T C TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr6:150004837T>C c.1388A>G c.(1387-1389)aAt>aGt p.N463S LUAD 6 150004968 150004968 + Missense_Mutation SNP C C T TCGA-80-5611-01A-01D-1625-08 TCGA-80-5611-10A-01D-1625-08 g.chr6:150004968C>T c.1257G>A c.(1255-1257)atG>atA p.M419I LUAD 6 150004976 150004976 + Missense_Mutation SNP G G C TCGA-91-6840-01A-11D-1945-08 TCGA-91-6840-10A-01D-1946-08 g.chr6:150004976G>C c.1249C>G c.(1249-1251)Cat>Gat p.H417D LUAD 6 150005349 150005349 + Frame_Shift_Del DEL T T - TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr6:150005349delT c.876delA c.(874-876)ccafs p.P293fs LUAD 6 150005698 150005698 + Missense_Mutation SNP T T A TCGA-MP-A4TC-01A-11D-A24P-08 TCGA-MP-A4TC-10A-01D-A24P-08 g.chr6:150005698T>A c.527A>T c.(526-528)cAg>cTg p.Q176L LUSC 6 149983278 149983278 + Missense_Mutation SNP C C T TCGA-66-2783-01A-01D-1267-08 TCGA-66-2783-11A-01D-1267-08 g.chr6:149983278C>T c.2980G>A c.(2980-2982)Gat>Aat p.D994N LUSC 6 149983369 149983369 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr6:149983369G>A c.2889C>T c.(2887-2889)atC>atT p.I963I LUSC 6 150001043 150001043 + Missense_Mutation SNP C C T TCGA-22-4604-01A-01D-1267-08 TCGA-22-4604-11A-01D-1267-08 g.chr6:150001043C>T c.2561G>A c.(2560-2562)aGa>aAa p.R854K LUSC 6 150004302 150004302 + Silent SNP G G A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr6:150004302G>A c.1923C>T c.(1921-1923)ttC>ttT p.F641F LUSC 6 150004707 150004707 + Silent SNP T T C TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chr6:150004707T>C c.1518A>G c.(1516-1518)ccA>ccG p.P506P LUSC 6 150005649 150005649 + Silent SNP C C A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr6:150005649C>A c.576G>T c.(574-576)ccG>ccT p.P192P LUSC 6 150023190 150023190 + Missense_Mutation SNP C C A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr6:150023190C>A c.73G>T c.(73-75)Gtc>Ttc p.V25F OV 6 149983176 149983176 + Missense_Mutation SNP G G T TCGA-13-0714-01A-01W-0370-10 TCGA-13-0714-10B-01W-0370-10 g.chr6:149983176G>T c.3082C>A c.(3082-3084)Cct>Act p.P1028T OV 6 149983199 149983199 + Missense_Mutation SNP C C G TCGA-04-1331-01A-01W-0486-08 TCGA-04-1331-10A-01W-0486-08 g.chr6:149983199C>G c.3059G>C c.(3058-3060)aGa>aCa p.R1020T OV 6 149997787 149997787 + Missense_Mutation SNP A A T TCGA-29-1699-01A-01W-0633-09 TCGA-29-1699-10A-01W-0633-09 g.chr6:149997787A>T c.2680T>A c.(2680-2682)Tta>Ata p.L894I OV 6 150001362 150001362 + Missense_Mutation SNP C C T TCGA-24-1419-01A-01W-0545-08 TCGA-24-1419-10A-01W-0545-08 g.chr6:150001362C>T c.2242G>A c.(2242-2244)Gct>Act p.A748T OV 6 150001524 150001524 + Missense_Mutation SNP G G A TCGA-24-1603-01A-01W-0551-08 TCGA-24-1603-10A-01W-0551-08 g.chr6:150001524G>A c.2080C>T c.(2080-2082)Cgt>Tgt p.R694C OV 6 150004239 150004239 + Silent SNP T T C TCGA-13-1489-01A-01W-0549-09 TCGA-13-1489-10A-01W-0549-09 g.chr6:150004239T>C c.1986A>G c.(1984-1986)aaA>aaG p.K662K OV 6 150004708 150004708 + Missense_Mutation SNP G G C TCGA-13-1483-01A-01W-0549-09 TCGA-13-1483-10A-01W-0549-09 g.chr6:150004708G>C c.1517C>G c.(1516-1518)cCa>cGa p.P506R OV 6 150023030 150023030 + Frame_Shift_Del DEL A A - TCGA-30-1891-01A-01W-0699-08 TCGA-30-1891-10A-01W-0699-08 g.chr6:150023030delA c.233delT c.(232-234)ttgfs p.L78fs PAAD 6 149982884 149982884 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:149982884C>T c.3374G>A c.(3373-3375)cGc>cAc p.R1125H PAAD 6 149983251 149983251 + Nonsense_Mutation SNP C C A TCGA-FB-AAQ3-01A-11D-A40W-08 TCGA-FB-AAQ3-11A-11D-A40W-08 g.chr6:149983251C>A c.3007G>T c.(3007-3009)Gaa>Taa p.E1003* PAAD 6 150001515 150001515 + Missense_Mutation SNP T T C TCGA-XN-A8T5-01A-12D-A36O-08 TCGA-XN-A8T5-10A-01D-A367-08 g.chr6:150001515T>C c.2089A>G c.(2089-2091)Agg>Ggg p.R697G PAAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-3A-A9I5-01A-11D-A38G-08 TCGA-3A-A9I5-10A-01D-A38J-08 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C PAAD 6 150004721 150004721 + Missense_Mutation SNP G G A TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr6:150004721G>A c.1504C>T c.(1504-1506)Cgt>Tgt p.R502C PRAD 6 150023045 150023045 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:150023045G>A c.218C>T c.(217-219)aCg>aTg p.T73M READ 6 149983274 149983274 + Missense_Mutation SNP C C T TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr6:149983274C>T c.2984G>A c.(2983-2985)cGc>cAc p.R995H READ 6 150001395 150001395 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:150001395G>A c.2209C>T c.(2209-2211)Cga>Tga p.R737* READ 6 150005395 150005395 + Missense_Mutation SNP T T C TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr6:150005395T>C c.830A>G c.(829-831)tAt>tGt p.Y277C SKCM 6 150004522 150004522 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr6:150004522G>A c.1703C>T c.(1702-1704)cCa>cTa p.P568L SKCM 6 150004748 150004748 + Missense_Mutation SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr6:150004748G>A c.1477C>T c.(1477-1479)Cct>Tct p.P493S SKCM 6 150005324 150005324 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr6:150005324G>A c.901C>T c.(901-903)Cct>Tct p.P301S SKCM 6 150005350 150005350 + Missense_Mutation SNP G G A TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr6:150005350G>A c.875C>T c.(874-876)cCa>cTa p.P292L SKCM 6 150005366 150005366 + Nonsense_Mutation SNP G G A TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr6:150005366G>A c.859C>T c.(859-861)Cga>Tga p.R287* SKCM 6 150005367 150005367 + Silent SNP G G A TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr6:150005367G>A c.858C>T c.(856-858)tcC>tcT p.S286S SKCM 6 150005421 150005421 + Nonsense_Mutation SNP C C T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr6:150005421C>T c.804G>A c.(802-804)tgG>tgA p.W268* SKCM 6 150022976 150022976 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr6:150022976C>T c.287G>A c.(286-288)cGg>cAg p.R96Q

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 6 150004708 150004708 single base substitution G A 3_prime_UTR_variant BLCA-CN 6 150004708 150004708 single base substitution G A downstream_gene_variant BLCA-CN 6 150004708 150004708 single base substitution G A exon_variant BLCA-CN 6 150004708 150004708 single base substitution G A missense_variant P506L 1517C>T BLCA-CN 6 150022925 150022925 single base substitution C T exon_variant BLCA-CN 6 150022925 150022925 single base substitution C T intron_variant BLCA-CN 6 150022925 150022925 single base substitution C T missense_variant G113E 338G>A BLCA-US 6 150001017 150001017 single base substitution G C 3_prime_UTR_variant BLCA-US 6 150001017 150001017 single base substitution G C downstream_gene_variant BLCA-US 6 150001017 150001017 single base substitution G C exon_variant BLCA-US 6 150001017 150001017 single base substitution G C missense_variant Q863E 2587C>G BLCA-US 6 150005065 150005065 single base substitution G A 3_prime_UTR_variant BLCA-US 6 150005065 150005065 single base substitution G A downstream_gene_variant BLCA-US 6 150005065 150005065 single base substitution G A exon_variant BLCA-US 6 150005065 150005065 single base substitution G A missense_variant S387F 1160C>T BLCA-US 6 150005361 150005361 single base substitution G C 3_prime_UTR_variant BLCA-US 6 150005361 150005361 single base substitution G C downstream_gene_variant BLCA-US 6 150005361 150005361 single base substitution G C exon_variant BLCA-US 6 150005361 150005361 single base substitution G C missense_variant I288M 864C>G BLCA-US 6 150023160 150023160 single base substitution G A exon_variant BLCA-US 6 150023160 150023160 single base substitution G A intron_variant BLCA-US 6 150023160 150023160 single base substitution G A missense_variant R35W 103C>T BLCA-US 6 150023160 150023160 single base substitution G A upstream_gene_variant BRCA-EU 6 149975539 149975539 single base substitution G A downstream_gene_variant BRCA-EU 6 149975850 149975850 single base substitution C G downstream_gene_variant BRCA-EU 6 149976148 149976148 single base substitution G A downstream_gene_variant BRCA-EU 6 149976749 149976749 single base substitution C T downstream_gene_variant BRCA-EU 6 149976854 149976854 single base substitution C G downstream_gene_variant BRCA-EU 6 149977888 149977888 single base substitution G C downstream_gene_variant BRCA-EU 6 149978209 149978209 single base substitution C T downstream_gene_variant BRCA-EU 6 149978620 149978620 single base substitution C G downstream_gene_variant BRCA-EU 6 149978928 149978928 single base substitution A C downstream_gene_variant BRCA-EU 6 149979066 149979066 single base substitution A G downstream_gene_variant BRCA-EU 6 149979235 149979235 single base substitution T C downstream_gene_variant BRCA-EU 6 149980181 149980234 multiple base substitution (>=2bp and <=200bp) AGTAGATGTAGTTTTGGAATAAGATAGCTGATAAGTATATCCAAACTGTTAAAA ATAGAATATACT 3_prime_UTR_variant BRCA-EU 6 149980181 149980234 multiple base substitution (>=2bp and <=200bp) AGTAGATGTAGTTTTGGAATAAGATAGCTGATAAGTATATCCAAACTGTTAAAA ATAGAATATACT downstream_gene_variant BRCA-EU 6 149980238 149980238 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 149980238 149980238 single base substitution C T downstream_gene_variant BRCA-EU 6 149980301 149980301 single base substitution T A 3_prime_UTR_variant BRCA-EU 6 149980301 149980301 single base substitution T A downstream_gene_variant BRCA-EU 6 149981298 149981298 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 6 149981298 149981298 deletion of <=200bp T - downstream_gene_variant BRCA-EU 6 149982912 149982912 single base substitution G C 3_prime_UTR_variant BRCA-EU 6 149982912 149982912 single base substitution G C missense_variant Q1116E 3346C>G BRCA-EU 6 149983043 149983043 single base substitution T C 3_prime_UTR_variant BRCA-EU 6 149983043 149983043 single base substitution T C missense_variant E1072G 3215A>G BRCA-EU 6 149986117 149986117 single base substitution C G intron_variant BRCA-EU 6 149986756 149986756 single base substitution C T intron_variant BRCA-EU 6 149987200 149987200 single base substitution C G intron_variant BRCA-EU 6 149987866 149987866 single base substitution C G intron_variant BRCA-EU 6 149988175 149988175 single base substitution G T intron_variant BRCA-EU 6 149989955 149989955 single base substitution G T intron_variant BRCA-EU 6 149991735 149991735 single base substitution C T intron_variant BRCA-EU 6 149991859 149991859 insertion of <=200bp - T downstream_gene_variant BRCA-EU 6 149991859 149991859 insertion of <=200bp - T intron_variant BRCA-EU 6 149992458 149992458 single base substitution C T downstream_gene_variant BRCA-EU 6 149992458 149992458 single base substitution C T intron_variant BRCA-EU 6 149992931 149992931 single base substitution C A downstream_gene_variant BRCA-EU 6 149992931 149992931 single base substitution C A intron_variant BRCA-EU 6 149993685 149993685 single base substitution C G downstream_gene_variant BRCA-EU 6 149993685 149993685 single base substitution C G intron_variant BRCA-EU 6 149996181 149996181 single base substitution C T downstream_gene_variant BRCA-EU 6 149996181 149996181 single base substitution C T intron_variant BRCA-EU 6 149997533 149997533 single base substitution T A intron_variant BRCA-EU 6 149997706 149997706 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 149997706 149997706 single base substitution C T exon_variant BRCA-EU 6 149997706 149997706 single base substitution C T missense_variant V921M 2761G>A BRCA-EU 6 149997801 149997801 single base substitution T C 3_prime_UTR_variant BRCA-EU 6 149997801 149997801 single base substitution T C exon_variant BRCA-EU 6 149997801 149997801 single base substitution T C missense_variant D889G 2666A>G BRCA-EU 6 149998220 149998220 single base substitution C T intron_variant BRCA-EU 6 149999793 149999793 single base substitution T C downstream_gene_variant BRCA-EU 6 149999793 149999793 single base substitution T C intron_variant BRCA-EU 6 149999886 149999886 single base substitution A T downstream_gene_variant BRCA-EU 6 149999886 149999886 single base substitution A T intron_variant BRCA-EU 6 150000118 150000118 single base substitution G T downstream_gene_variant BRCA-EU 6 150000118 150000118 single base substitution G T intron_variant BRCA-EU 6 150000372 150000372 single base substitution G C downstream_gene_variant BRCA-EU 6 150000372 150000372 single base substitution G C intron_variant BRCA-EU 6 150000883 150000883 single base substitution C G downstream_gene_variant BRCA-EU 6 150000883 150000883 single base substitution C G intron_variant BRCA-EU 6 150000921 150000921 single base substitution C G downstream_gene_variant BRCA-EU 6 150000921 150000921 single base substitution C G intron_variant BRCA-EU 6 150005768 150005768 deletion of <=200bp T - intron_variant BRCA-EU 6 150005778 150005778 single base substitution C G intron_variant BRCA-EU 6 150010191 150010191 single base substitution C A intron_variant BRCA-EU 6 150011466 150011466 single base substitution C G intron_variant BRCA-EU 6 150014401 150014401 single base substitution C G intron_variant BRCA-EU 6 150017058 150017058 single base substitution G A intron_variant BRCA-EU 6 150017494 150017494 single base substitution C T intron_variant BRCA-EU 6 150019555 150019555 insertion of <=200bp - T intron_variant BRCA-EU 6 150019769 150019769 single base substitution C A intron_variant BRCA-EU 6 150019841 150019841 single base substitution C A intron_variant BRCA-EU 6 150020290 150020290 single base substitution G C intron_variant BRCA-EU 6 150021603 150021603 single base substitution C T intron_variant BRCA-EU 6 150021966 150021966 single base substitution C A intron_variant BRCA-EU 6 150022839 150022839 single base substitution G A intron_variant BRCA-EU 6 150023329 150023329 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 6 150023329 150023329 single base substitution G C intron_variant BRCA-EU 6 150023329 150023329 single base substitution G C upstream_gene_variant BRCA-EU 6 150023619 150023619 single base substitution T A intron_variant BRCA-EU 6 150023619 150023619 single base substitution T A upstream_gene_variant BRCA-EU 6 150023874 150023874 single base substitution C G intron_variant BRCA-EU 6 150023874 150023874 single base substitution C G upstream_gene_variant BRCA-EU 6 150024335 150024335 single base substitution T A intron_variant BRCA-EU 6 150024335 150024335 single base substitution T A upstream_gene_variant BRCA-EU 6 150025421 150025421 single base substitution G A intron_variant BRCA-EU 6 150025421 150025421 single base substitution G A upstream_gene_variant BRCA-EU 6 150026193 150026193 single base substitution C T intron_variant BRCA-EU 6 150026193 150026193 single base substitution C T upstream_gene_variant BRCA-EU 6 150026982 150026982 single base substitution C G intron_variant BRCA-EU 6 150026982 150026982 single base substitution C G upstream_gene_variant BRCA-EU 6 150027538 150027538 single base substitution C A intron_variant BRCA-EU 6 150027538 150027538 single base substitution C A upstream_gene_variant BRCA-EU 6 150027800 150027800 single base substitution C A intron_variant BRCA-EU 6 150027800 150027800 single base substitution C A upstream_gene_variant BRCA-EU 6 150029158 150029158 deletion of <=200bp A - intron_variant BRCA-EU 6 150031473 150031473 single base substitution C G intron_variant BRCA-EU 6 150031484 150031484 single base substitution G A intron_variant BRCA-EU 6 150031525 150031525 single base substitution T C intron_variant BRCA-EU 6 150035939 150035939 single base substitution T C intron_variant BRCA-EU 6 150036448 150036448 single base substitution G A intron_variant BRCA-EU 6 150038801 150038801 single base substitution C T intron_variant BRCA-EU 6 150038801 150038801 single base substitution C T upstream_gene_variant BRCA-EU 6 150038942 150038942 single base substitution G T intron_variant BRCA-EU 6 150038942 150038942 single base substitution G T upstream_gene_variant BRCA-EU 6 150040360 150040360 single base substitution C T upstream_gene_variant BRCA-EU 6 150041820 150041820 single base substitution A G upstream_gene_variant BRCA-FR 6 149978209 149978209 single base substitution C T downstream_gene_variant BRCA-FR 6 149990132 149990132 single base substitution A T intron_variant BRCA-FR 6 149998220 149998220 single base substitution C T intron_variant BRCA-FR 6 150017494 150017494 single base substitution C T intron_variant BRCA-FR 6 150020290 150020290 single base substitution G C intron_variant BRCA-UK 6 149978928 149978928 single base substitution A C downstream_gene_variant BRCA-UK 6 149982912 149982912 single base substitution G C 3_prime_UTR_variant BRCA-UK 6 149982912 149982912 single base substitution G C missense_variant Q1116E 3346C>G BRCA-UK 6 150001755 150001755 single base substitution C T downstream_gene_variant BRCA-UK 6 150001755 150001755 single base substitution C T intron_variant BRCA-UK 6 150016283 150016283 single base substitution C T 3_prime_UTR_variant BRCA-UK 6 150016283 150016283 single base substitution C T exon_variant BRCA-UK 6 150016283 150016283 single base substitution C T missense_variant M141I 423G>A BRCA-UK 6 150016283 150016283 single base substitution C T missense_variant M87I 261G>A BRCA-UK 6 150025548 150025548 single base substitution C G intron_variant BRCA-UK 6 150025548 150025548 single base substitution C G upstream_gene_variant BRCA-UK 6 150034165 150034165 single base substitution C T intron_variant BRCA-US 6 149983176 149983176 single base substitution G C 3_prime_UTR_variant BRCA-US 6 149983176 149983176 single base substitution G C missense_variant P1028A 3082C>G BRCA-US 6 149983263 149983263 single base substitution T C 3_prime_UTR_variant BRCA-US 6 149983263 149983263 single base substitution T C missense_variant N999D 2995A>G BRCA-US 6 150001092 150001092 single base substitution G C 3_prime_UTR_variant BRCA-US 6 150001092 150001092 single base substitution G C downstream_gene_variant BRCA-US 6 150001092 150001092 single base substitution G C exon_variant BRCA-US 6 150001092 150001092 single base substitution G C missense_variant R838G 2512C>G BRCA-US 6 150005196 150005196 single base substitution C T 3_prime_UTR_variant BRCA-US 6 150005196 150005196 single base substitution C T downstream_gene_variant BRCA-US 6 150005196 150005196 single base substitution C T exon_variant BRCA-US 6 150005196 150005196 single base substitution C T synonymous_variant G343G 1029G>A BRCA-US 6 150023155 150023155 single base substitution T A exon_variant BRCA-US 6 150023155 150023155 single base substitution T A intron_variant BRCA-US 6 150023155 150023155 single base substitution T A missense_variant E36D 108A>T BRCA-US 6 150023155 150023155 single base substitution T A upstream_gene_variant BRCA-US 6 150039148 150039148 single base substitution G A 5_prime_UTR_variant BRCA-US 6 150039148 150039148 single base substitution G A missense_variant S8L 23C>T BRCA-US 6 150039148 150039148 single base substitution G A upstream_gene_variant BTCA-JP 6 149983071 149983071 single base substitution C A 3_prime_UTR_variant BTCA-JP 6 149983071 149983071 single base substitution C A stop_gained G1063* 3187G>T BTCA-JP 6 150004239 150004239 deletion of <=200bp T - 3_prime_UTR_variant BTCA-JP 6 150004239 150004239 deletion of <=200bp T - downstream_gene_variant BTCA-JP 6 150004239 150004239 deletion of <=200bp T - exon_variant BTCA-JP 6 150004239 150004239 deletion of <=200bp T - frameshift_variant K662 BTCA-JP 6 150004910 150004910 single base substitution C T 3_prime_UTR_variant BTCA-JP 6 150004910 150004910 single base substitution C T downstream_gene_variant BTCA-JP 6 150004910 150004910 single base substitution C T exon_variant BTCA-JP 6 150004910 150004910 single base substitution C T missense_variant A439T 1315G>A CESC-US 6 149983239 149983239 single base substitution G A 3_prime_UTR_variant CESC-US 6 149983239 149983239 single base substitution G A missense_variant H1007Y 3019C>T CESC-US 6 149997435 149997435 single base substitution A C 3_prime_UTR_variant CESC-US 6 149997435 149997435 single base substitution A C exon_variant CESC-US 6 149997435 149997435 single base substitution A C synonymous_variant P948P 2844T>G CESC-US 6 149997469 149997469 single base substitution C A 3_prime_UTR_variant CESC-US 6 149997469 149997469 single base substitution C A exon_variant CESC-US 6 149997469 149997469 single base substitution C A missense_variant G937V 2810G>T CESC-US 6 149997697 149997697 single base substitution G A 3_prime_UTR_variant CESC-US 6 149997697 149997697 single base substitution G A exon_variant CESC-US 6 149997697 149997697 single base substitution G A stop_gained R924* 2770C>T CESC-US 6 150001486 150001486 single base substitution C A 3_prime_UTR_variant CESC-US 6 150001486 150001486 single base substitution C A downstream_gene_variant CESC-US 6 150001486 150001486 single base substitution C A exon_variant CESC-US 6 150001486 150001486 single base substitution C A synonymous_variant V706V 2118G>T CESC-US 6 150001559 150001559 single base substitution C G 3_prime_UTR_variant CESC-US 6 150001559 150001559 single base substitution C G downstream_gene_variant CESC-US 6 150001559 150001559 single base substitution C G exon_variant CESC-US 6 150001559 150001559 single base substitution C G missense_variant R682T 2045G>C CESC-US 6 150004568 150004568 single base substitution G C 3_prime_UTR_variant CESC-US 6 150004568 150004568 single base substitution G C downstream_gene_variant CESC-US 6 150004568 150004568 single base substitution G C exon_variant CESC-US 6 150004568 150004568 single base substitution G C missense_variant Q553E 1657C>G CESC-US 6 150004621 150004621 single base substitution C T 3_prime_UTR_variant CESC-US 6 150004621 150004621 single base substitution C T downstream_gene_variant CESC-US 6 150004621 150004621 single base substitution C T exon_variant CESC-US 6 150004621 150004621 single base substitution C T missense_variant G535E 1604G>A CESC-US 6 150005408 150005408 single base substitution G A 3_prime_UTR_variant CESC-US 6 150005408 150005408 single base substitution G A downstream_gene_variant CESC-US 6 150005408 150005408 single base substitution G A exon_variant CESC-US 6 150005408 150005408 single base substitution G A stop_gained Q273* 817C>T CESC-US 6 150005474 150005474 single base substitution G C 3_prime_UTR_variant CESC-US 6 150005474 150005474 single base substitution G C downstream_gene_variant CESC-US 6 150005474 150005474 single base substitution G C exon_variant CESC-US 6 150005474 150005474 single base substitution G C missense_variant P197A 589C>G CESC-US 6 150005474 150005474 single base substitution G C missense_variant P251A 751C>G CESC-US 6 150005552 150005552 single base substitution G C 3_prime_UTR_variant CESC-US 6 150005552 150005552 single base substitution G C exon_variant CESC-US 6 150005552 150005552 single base substitution G C missense_variant Q171E 511C>G CESC-US 6 150005552 150005552 single base substitution G C missense_variant Q225E 673C>G CESC-US 6 150005605 150005605 single base substitution G C 3_prime_UTR_variant CESC-US 6 150005605 150005605 single base substitution G C exon_variant CESC-US 6 150005605 150005605 single base substitution G C stop_gained S153* 458C>G CESC-US 6 150005605 150005605 single base substitution G C stop_gained S207* 620C>G CESC-US 6 150016267 150016267 single base substitution G A 3_prime_UTR_variant CESC-US 6 150016267 150016267 single base substitution G A exon_variant CESC-US 6 150016267 150016267 single base substitution G A stop_gained R147* 439C>T CESC-US 6 150016267 150016267 single base substitution G A stop_gained R93* 277C>T CLLE-ES 6 150025628 150025628 single base substitution T G intron_variant CLLE-ES 6 150025628 150025628 single base substitution T G upstream_gene_variant COAD-US 6 149982976 149982976 single base substitution C T 3_prime_UTR_variant COAD-US 6 149982976 149982976 single base substitution C T synonymous_variant P1094P 3282G>A COAD-US 6 149983216 149983216 single base substitution G A 3_prime_UTR_variant COAD-US 6 149983216 149983216 single base substitution G A synonymous_variant D1014D 3042C>T COAD-US 6 149997822 149997822 single base substitution G T 3_prime_UTR_variant COAD-US 6 149997822 149997822 single base substitution G T exon_variant COAD-US 6 149997822 149997822 single base substitution G T missense_variant P882H 2645C>A COAD-US 6 150001188 150001188 single base substitution G A 3_prime_UTR_variant COAD-US 6 150001188 150001188 single base substitution G A downstream_gene_variant COAD-US 6 150001188 150001188 single base substitution G A exon_variant COAD-US 6 150001188 150001188 single base substitution G A stop_gained R806* 2416C>T COAD-US 6 150001540 150001540 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 6 150001540 150001540 deletion of <=200bp T - downstream_gene_variant COAD-US 6 150001540 150001540 deletion of <=200bp T - exon_variant COAD-US 6 150001540 150001540 deletion of <=200bp T - frameshift_variant K688 COAD-US 6 150004239 150004239 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 6 150004239 150004239 deletion of <=200bp T - downstream_gene_variant COAD-US 6 150004239 150004239 deletion of <=200bp T - exon_variant COAD-US 6 150004239 150004239 deletion of <=200bp T - frameshift_variant K662 COAD-US 6 150004556 150004556 single base substitution G A 3_prime_UTR_variant COAD-US 6 150004556 150004556 single base substitution G A downstream_gene_variant COAD-US 6 150004556 150004556 single base substitution G A exon_variant COAD-US 6 150004556 150004556 single base substitution G A missense_variant P557S 1669C>T COAD-US 6 150004779 150004779 single base substitution A G 3_prime_UTR_variant COAD-US 6 150004779 150004779 single base substitution A G downstream_gene_variant COAD-US 6 150004779 150004779 single base substitution A G exon_variant COAD-US 6 150004779 150004779 single base substitution A G synonymous_variant S482S 1446T>C COAD-US 6 150005250 150005250 single base substitution A G 3_prime_UTR_variant COAD-US 6 150005250 150005250 single base substitution A G downstream_gene_variant COAD-US 6 150005250 150005250 single base substitution A G exon_variant COAD-US 6 150005250 150005250 single base substitution A G synonymous_variant V325V 975T>C COAD-US 6 150023084 150023084 single base substitution T C exon_variant COAD-US 6 150023084 150023084 single base substitution T C intron_variant COAD-US 6 150023084 150023084 single base substitution T C missense_variant E60G 179A>G COCA-CN 6 149982836 149982836 single base substitution A C 3_prime_UTR_variant COCA-CN 6 149983262 149983262 single base substitution T G 3_prime_UTR_variant COCA-CN 6 149983262 149983262 single base substitution T G missense_variant N999T 2996A>C COCA-CN 6 149997697 149997697 single base substitution G A 3_prime_UTR_variant COCA-CN 6 149997697 149997697 single base substitution G A exon_variant COCA-CN 6 149997697 149997697 single base substitution G A stop_gained R924* 2770C>T COCA-CN 6 149999105 149999105 single base substitution G A downstream_gene_variant COCA-CN 6 149999105 149999105 single base substitution G A intron_variant COCA-CN 6 150001373 150001373 single base substitution C T 3_prime_UTR_variant COCA-CN 6 150001373 150001373 single base substitution C T downstream_gene_variant COCA-CN 6 150001373 150001373 single base substitution C T exon_variant COCA-CN 6 150001373 150001373 single base substitution C T missense_variant R744Q 2231G>A COCA-CN 6 150001394 150001394 single base substitution C T 3_prime_UTR_variant COCA-CN 6 150001394 150001394 single base substitution C T downstream_gene_variant COCA-CN 6 150001394 150001394 single base substitution C T exon_variant COCA-CN 6 150001394 150001394 single base substitution C T missense_variant R737Q 2210G>A COCA-CN 6 150004506 150004506 single base substitution G A 3_prime_UTR_variant COCA-CN 6 150004506 150004506 single base substitution G A downstream_gene_variant COCA-CN 6 150004506 150004506 single base substitution G A exon_variant COCA-CN 6 150004506 150004506 single base substitution G A synonymous_variant Y573Y 1719C>T COCA-CN 6 150004671 150004671 single base substitution A C 3_prime_UTR_variant COCA-CN 6 150004671 150004671 single base substitution A C downstream_gene_variant COCA-CN 6 150004671 150004671 single base substitution A C exon_variant COCA-CN 6 150004671 150004671 single base substitution A C synonymous_variant S518S 1554T>G COCA-CN 6 150004703 150004703 single base substitution G A 3_prime_UTR_variant COCA-CN 6 150004703 150004703 single base substitution G A downstream_gene_variant COCA-CN 6 150004703 150004703 single base substitution G A exon_variant COCA-CN 6 150004703 150004703 single base substitution G A synonymous_variant L508L 1522C>T COCA-CN 6 150005760 150005760 single base substitution G T intron_variant COCA-CN 6 150018266 150018266 single base substitution A C exon_variant COCA-CN 6 150018266 150018266 single base substitution A C intron_variant COCA-CN 6 150022982 150022982 single base substitution G T exon_variant COCA-CN 6 150022982 150022982 single base substitution G T intron_variant COCA-CN 6 150022982 150022982 single base substitution G T missense_variant S94Y 281C>A COCA-CN 6 150023019 150023019 single base substitution G A exon_variant COCA-CN 6 150023019 150023019 single base substitution G A intron_variant COCA-CN 6 150023019 150023019 single base substitution G A stop_gained R82* 244C>T COCA-CN 6 150039271 150039271 single base substitution C T 5_prime_UTR_variant COCA-CN 6 150039271 150039271 single base substitution C T upstream_gene_variant EOPC-DE 6 150011744 150011744 single base substitution G A intron_variant ESAD-UK 6 149974834 149974834 single base substitution T G downstream_gene_variant ESAD-UK 6 149974989 149974989 single base substitution A C downstream_gene_variant ESAD-UK 6 149975560 149975560 single base substitution C T downstream_gene_variant ESAD-UK 6 149975622 149975622 single base substitution T G downstream_gene_variant ESAD-UK 6 149976279 149976279 deletion of <=200bp T - downstream_gene_variant ESAD-UK 6 149976310 149976310 single base substitution A G downstream_gene_variant ESAD-UK 6 149976603 149976603 single base substitution G C downstream_gene_variant ESAD-UK 6 149979138 149979138 single base substitution G A downstream_gene_variant ESAD-UK 6 149979416 149979416 single base substitution G A 3_prime_UTR_variant ESAD-UK 6 149979416 149979416 single base substitution G A downstream_gene_variant ESAD-UK 6 149985028 149985028 single base substitution C T intron_variant ESAD-UK 6 149985134 149985134 single base substitution C T intron_variant ESAD-UK 6 149985330 149985330 single base substitution A T intron_variant ESAD-UK 6 149988252 149988252 deletion of <=200bp A - intron_variant ESAD-UK 6 149988537 149988537 single base substitution C T intron_variant ESAD-UK 6 149989173 149989173 single base substitution C T intron_variant ESAD-UK 6 149990126 149990126 single base substitution A T intron_variant ESAD-UK 6 149990386 149990386 single base substitution C T intron_variant ESAD-UK 6 149994240 149994240 single base substitution T C downstream_gene_variant ESAD-UK 6 149994240 149994240 single base substitution T C intron_variant ESAD-UK 6 149995221 149995221 deletion of <=200bp T - downstream_gene_variant ESAD-UK 6 149995221 149995221 deletion of <=200bp T - intron_variant ESAD-UK 6 149995485 149995485 single base substitution A G downstream_gene_variant ESAD-UK 6 149995485 149995485 single base substitution A G intron_variant ESAD-UK 6 149998078 149998078 deletion of <=200bp A - intron_variant ESAD-UK 6 149998344 149998344 single base substitution T C intron_variant ESAD-UK 6 150000548 150000548 single base substitution C T downstream_gene_variant ESAD-UK 6 150000548 150000548 single base substitution C T intron_variant ESAD-UK 6 150000791 150000791 single base substitution A T downstream_gene_variant ESAD-UK 6 150000791 150000791 single base substitution A T intron_variant ESAD-UK 6 150002020 150002020 insertion of <=200bp - A downstream_gene_variant ESAD-UK 6 150002020 150002020 insertion of <=200bp - A intron_variant ESAD-UK 6 150002305 150002329 deletion of <=200bp ATGAAAATATCAAAAAATAGATTAA - downstream_gene_variant ESAD-UK 6 150002305 150002329 deletion of <=200bp ATGAAAATATCAAAAAATAGATTAA - intron_variant ESAD-UK 6 150002573 150002573 single base substitution T A downstream_gene_variant ESAD-UK 6 150002573 150002573 single base substitution T A intron_variant ESAD-UK 6 150004449 150004449 single base substitution C G 3_prime_UTR_variant ESAD-UK 6 150004449 150004449 single base substitution C G downstream_gene_variant ESAD-UK 6 150004449 150004449 single base substitution C G exon_variant ESAD-UK 6 150004449 150004449 single base substitution C G missense_variant E592D 1776G>C ESAD-UK 6 150007548 150007548 single base substitution C A intron_variant ESAD-UK 6 150008517 150008517 single base substitution G A intron_variant ESAD-UK 6 150009408 150009408 single base substitution C G intron_variant ESAD-UK 6 150009603 150009603 single base substitution C T intron_variant ESAD-UK 6 150011619 150011619 single base substitution G A intron_variant ESAD-UK 6 150012439 150012439 single base substitution C T intron_variant ESAD-UK 6 150013717 150013717 single base substitution A G intron_variant ESAD-UK 6 150014748 150014751 deletion of <=200bp AAAC - intron_variant ESAD-UK 6 150016700 150016700 single base substitution C T intron_variant ESAD-UK 6 150018907 150018907 single base substitution G A intron_variant ESAD-UK 6 150019597 150019597 single base substitution G C intron_variant ESAD-UK 6 150020688 150020688 single base substitution C T intron_variant ESAD-UK 6 150024266 150024266 single base substitution C T intron_variant ESAD-UK 6 150024266 150024266 single base substitution C T upstream_gene_variant ESAD-UK 6 150024325 150024325 single base substitution G A intron_variant ESAD-UK 6 150024325 150024325 single base substitution G A upstream_gene_variant ESAD-UK 6 150025628 150025628 single base substitution T G intron_variant ESAD-UK 6 150025628 150025628 single base substitution T G upstream_gene_variant ESAD-UK 6 150025629 150025629 single base substitution G T intron_variant ESAD-UK 6 150025629 150025629 single base substitution G T upstream_gene_variant ESAD-UK 6 150026957 150026957 single base substitution G C intron_variant ESAD-UK 6 150026957 150026957 single base substitution G C upstream_gene_variant ESAD-UK 6 150027489 150027489 insertion of <=200bp - A intron_variant ESAD-UK 6 150027489 150027489 insertion of <=200bp - A upstream_gene_variant ESAD-UK 6 150034048 150034048 deletion of <=200bp T - intron_variant ESAD-UK 6 150034701 150034701 single base substitution C T intron_variant ESAD-UK 6 150036741 150036741 deletion of <=200bp A - intron_variant ESAD-UK 6 150039376 150039376 single base substitution T C 5_prime_UTR_variant ESAD-UK 6 150039376 150039376 single base substitution T C upstream_gene_variant ESCA-CN 6 150001170 150001170 single base substitution G A 3_prime_UTR_variant ESCA-CN 6 150001170 150001170 single base substitution G A downstream_gene_variant ESCA-CN 6 150001170 150001170 single base substitution G A exon_variant ESCA-CN 6 150001170 150001170 single base substitution G A missense_variant L812F 2434C>T ESCA-CN 6 150039148 150039148 single base substitution G A 5_prime_UTR_variant ESCA-CN 6 150039148 150039148 single base substitution G A missense_variant S8L 23C>T ESCA-CN 6 150039148 150039148 single base substitution G A upstream_gene_variant KIRC-US 6 150001249 150001249 single base substitution A G 3_prime_UTR_variant KIRC-US 6 150001249 150001249 single base substitution A G downstream_gene_variant KIRC-US 6 150001249 150001249 single base substitution A G exon_variant KIRC-US 6 150001249 150001249 single base substitution A G synonymous_variant I785I 2355T>C KIRC-US 6 150004564 150004564 single base substitution C T 3_prime_UTR_variant KIRC-US 6 150004564 150004564 single base substitution C T downstream_gene_variant KIRC-US 6 150004564 150004564 single base substitution C T exon_variant KIRC-US 6 150004564 150004564 single base substitution C T missense_variant G554E 1661G>A KIRC-US 6 150023180 150023180 single base substitution C T exon_variant KIRC-US 6 150023180 150023180 single base substitution C T intron_variant KIRC-US 6 150023180 150023180 single base substitution C T missense_variant R28Q 83G>A KIRC-US 6 150023180 150023180 single base substitution C T upstream_gene_variant KIRP-US 6 149997827 149997827 single base substitution C G 3_prime_UTR_variant KIRP-US 6 149997827 149997827 single base substitution C G exon_variant KIRP-US 6 149997827 149997827 single base substitution C G synonymous_variant G880G 2640G>C KIRP-US 6 150001515 150001515 single base substitution T C 3_prime_UTR_variant KIRP-US 6 150001515 150001515 single base substitution T C downstream_gene_variant KIRP-US 6 150001515 150001515 single base substitution T C exon_variant KIRP-US 6 150001515 150001515 single base substitution T C missense_variant R697G 2089A>G KIRP-US 6 150005370 150005370 single base substitution G T 3_prime_UTR_variant KIRP-US 6 150005370 150005370 single base substitution G T downstream_gene_variant KIRP-US 6 150005370 150005370 single base substitution G T exon_variant KIRP-US 6 150005370 150005370 single base substitution G T synonymous_variant I285I 855C>A LAML-KR 6 149997657 149997657 single base substitution T C intron_variant LAML-KR 6 150001120 150001120 single base substitution A G 3_prime_UTR_variant LAML-KR 6 150001120 150001120 single base substitution A G downstream_gene_variant LAML-KR 6 150001120 150001120 single base substitution A G exon_variant LAML-KR 6 150001120 150001120 single base substitution A G synonymous_variant D828D 2484T>C LAML-KR 6 150014690 150014690 single base substitution G A intron_variant LGG-US 6 150005515 150005515 deletion of <=200bp G - 3_prime_UTR_variant LGG-US 6 150005515 150005515 deletion of <=200bp G - downstream_gene_variant LGG-US 6 150005515 150005515 deletion of <=200bp G - exon_variant LGG-US 6 150005515 150005515 deletion of <=200bp G - frameshift_variant P183 LGG-US 6 150005515 150005515 deletion of <=200bp G - frameshift_variant P237 LICA-CN 6 150004821 150004821 single base substitution T C 3_prime_UTR_variant LICA-CN 6 150004821 150004821 single base substitution T C downstream_gene_variant LICA-CN 6 150004821 150004821 single base substitution T C exon_variant LICA-CN 6 150004821 150004821 single base substitution T C synonymous_variant P468P 1404A>G LICA-CN 6 150023259 150023259 single base substitution T C exon_variant LICA-CN 6 150023259 150023259 single base substitution T C intron_variant LICA-CN 6 150023259 150023259 single base substitution T C missense_variant K2E 4A>G LICA-CN 6 150023259 150023259 single base substitution T C upstream_gene_variant LICA-CN 6 150023262 150023262 single base substitution T A exon_variant LICA-CN 6 150023262 150023262 single base substitution T A initiator_codon_variant M1L 1A>T LICA-CN 6 150023262 150023262 single base substitution T A intron_variant LICA-CN 6 150023262 150023262 single base substitution T A upstream_gene_variant LICA-FR 6 149997395 149997395 single base substitution C A exon_variant LICA-FR 6 149997395 149997395 single base substitution C A splice_donor_variant LICA-FR 6 150018353 150018353 single base substitution A C intron_variant LIHC-US 6 149997708 149997708 single base substitution T C 3_prime_UTR_variant LIHC-US 6 149997708 149997708 single base substitution T C exon_variant LIHC-US 6 149997708 149997708 single base substitution T C missense_variant E920G 2759A>G LIHC-US 6 150001056 150001058 deletion of <=200bp AGA - 3_prime_UTR_variant LIHC-US 6 150001056 150001058 deletion of <=200bp AGA - disruptive_inframe_deletion LC849R LIHC-US 6 150001056 150001058 deletion of <=200bp AGA - downstream_gene_variant LIHC-US 6 150001056 150001058 deletion of <=200bp AGA - exon_variant LINC-JP 6 149983228 149983228 single base substitution A T 3_prime_UTR_variant LINC-JP 6 149983228 149983228 single base substitution A T missense_variant F1010L 3030T>A LINC-JP 6 149983333 149983333 single base substitution A G 3_prime_UTR_variant LINC-JP 6 149983333 149983333 single base substitution A G synonymous_variant A975A 2925T>C LINC-JP 6 149983644 149983644 single base substitution T C intron_variant LINC-JP 6 149994337 149994337 single base substitution G C downstream_gene_variant LINC-JP 6 149994337 149994337 single base substitution G C intron_variant LINC-JP 6 149997729 149997729 single base substitution G A 3_prime_UTR_variant LINC-JP 6 149997729 149997729 single base substitution G A exon_variant LINC-JP 6 149997729 149997729 single base substitution G A missense_variant T913I 2738C>T LINC-JP 6 149997819 149997819 single base substitution G C 3_prime_UTR_variant LINC-JP 6 149997819 149997819 single base substitution G C exon_variant LINC-JP 6 149997819 149997819 single base substitution G C stop_gained S883* 2648C>G LINC-JP 6 150001319 150001319 single base substitution T A 3_prime_UTR_variant LINC-JP 6 150001319 150001319 single base substitution T A downstream_gene_variant LINC-JP 6 150001319 150001319 single base substitution T A exon_variant LINC-JP 6 150001319 150001319 single base substitution T A missense_variant N762I 2285A>T LINC-JP 6 150002814 150002814 single base substitution T A downstream_gene_variant LINC-JP 6 150002814 150002814 single base substitution T A intron_variant LINC-JP 6 150007041 150007041 single base substitution T C intron_variant LINC-JP 6 150008525 150008525 single base substitution C A intron_variant LINC-JP 6 150022994 150022994 single base substitution T C exon_variant LINC-JP 6 150022994 150022994 single base substitution T C intron_variant LINC-JP 6 150022994 150022994 single base substitution T C missense_variant N90S 269A>G LINC-JP 6 150023088 150023088 single base substitution T C exon_variant LINC-JP 6 150023088 150023088 single base substitution T C intron_variant LINC-JP 6 150023088 150023088 single base substitution T C missense_variant T59A 175A>G LINC-JP 6 150024122 150024122 single base substitution G A intron_variant LINC-JP 6 150024122 150024122 single base substitution G A upstream_gene_variant LINC-JP 6 150028650 150028650 single base substitution T C intron_variant LINC-JP 6 150033256 150033264 deletion of <=200bp CAGGGCCCA - intron_variant LINC-JP 6 150036406 150036406 single base substitution T C intron_variant LINC-JP 6 150038098 150038098 single base substitution C T intron_variant LINC-JP 6 150038098 150038098 single base substitution C T upstream_gene_variant LINC-JP 6 150038100 150038100 single base substitution G T intron_variant LINC-JP 6 150038100 150038100 single base substitution G T upstream_gene_variant LIRI-JP 6 149975085 149975086 deletion of <=200bp TT - downstream_gene_variant LIRI-JP 6 149975552 149975552 single base substitution C A downstream_gene_variant LIRI-JP 6 149975719 149975719 single base substitution G A downstream_gene_variant LIRI-JP 6 149976364 149976364 single base substitution G A downstream_gene_variant LIRI-JP 6 149976459 149976459 single base substitution A G downstream_gene_variant LIRI-JP 6 149979976 149979976 insertion of <=200bp - T 3_prime_UTR_variant LIRI-JP 6 149979976 149979976 insertion of <=200bp - T downstream_gene_variant LIRI-JP 6 149980118 149980118 single base substitution A G 3_prime_UTR_variant LIRI-JP 6 149980118 149980118 single base substitution A G downstream_gene_variant LIRI-JP 6 149981438 149981438 single base substitution C T 3_prime_UTR_variant LIRI-JP 6 149981438 149981438 single base substitution C T downstream_gene_variant LIRI-JP 6 149982725 149982725 insertion of <=200bp - A 3_prime_UTR_variant LIRI-JP 6 149982725 149982725 insertion of <=200bp - A downstream_gene_variant LIRI-JP 6 149983909 149983909 single base substitution G T intron_variant LIRI-JP 6 149988247 149988247 single base substitution A G intron_variant LIRI-JP 6 149988722 149988722 single base substitution C T intron_variant LIRI-JP 6 149988975 149988975 single base substitution T C intron_variant LIRI-JP 6 149992544 149992544 single base substitution A T downstream_gene_variant LIRI-JP 6 149992544 149992544 single base substitution A T intron_variant LIRI-JP 6 149994937 149994937 single base substitution T C downstream_gene_variant LIRI-JP 6 149994937 149994937 single base substitution T C intron_variant LIRI-JP 6 149998667 149998667 single base substitution T C intron_variant LIRI-JP 6 149999372 149999372 single base substitution C T downstream_gene_variant LIRI-JP 6 149999372 149999372 single base substitution C T intron_variant LIRI-JP 6 150001247 150001247 single base substitution G T 3_prime_UTR_variant LIRI-JP 6 150001247 150001247 single base substitution G T downstream_gene_variant LIRI-JP 6 150001247 150001247 single base substitution G T exon_variant LIRI-JP 6 150001247 150001247 single base substitution G T missense_variant P786H 2357C>A LIRI-JP 6 150001315 150001315 single base substitution T C 3_prime_UTR_variant LIRI-JP 6 150001315 150001315 single base substitution T C downstream_gene_variant LIRI-JP 6 150001315 150001315 single base substitution T C exon_variant LIRI-JP 6 150001315 150001315 single base substitution T C synonymous_variant E763E 2289A>G LIRI-JP 6 150001524 150001524 single base substitution G A 3_prime_UTR_variant LIRI-JP 6 150001524 150001524 single base substitution G A downstream_gene_variant LIRI-JP 6 150001524 150001524 single base substitution G A exon_variant LIRI-JP 6 150001524 150001524 single base substitution G A missense_variant R694C 2080C>T LIRI-JP 6 150002051 150002051 single base substitution T C downstream_gene_variant LIRI-JP 6 150002051 150002051 single base substitution T C intron_variant LIRI-JP 6 150002603 150002603 single base substitution A G downstream_gene_variant LIRI-JP 6 150002603 150002603 single base substitution A G intron_variant LIRI-JP 6 150004294 150004294 single base substitution T C 3_prime_UTR_variant LIRI-JP 6 150004294 150004294 single base substitution T C downstream_gene_variant LIRI-JP 6 150004294 150004294 single base substitution T C exon_variant LIRI-JP 6 150004294 150004294 single base substitution T C missense_variant E644G 1931A>G LIRI-JP 6 150006549 150006549 single base substitution C T intron_variant LIRI-JP 6 150007177 150007177 single base substitution T C intron_variant LIRI-JP 6 150008517 150008517 single base substitution G A intron_variant LIRI-JP 6 150008861 150008861 single base substitution G A intron_variant LIRI-JP 6 150010160 150010160 single base substitution T A intron_variant LIRI-JP 6 150010920 150010920 single base substitution G A intron_variant LIRI-JP 6 150011599 150011599 single base substitution C A intron_variant LIRI-JP 6 150012193 150012193 single base substitution T C intron_variant LIRI-JP 6 150013066 150013066 single base substitution T C intron_variant LIRI-JP 6 150017353 150017356 deletion of <=200bp TATA - intron_variant LIRI-JP 6 150020800 150020800 single base substitution C A intron_variant LIRI-JP 6 150023783 150023783 single base substitution T C intron_variant LIRI-JP 6 150023783 150023783 single base substitution T C upstream_gene_variant LIRI-JP 6 150025358 150025358 single base substitution C T intron_variant LIRI-JP 6 150025358 150025358 single base substitution C T upstream_gene_variant LIRI-JP 6 150026088 150026088 single base substitution A G intron_variant LIRI-JP 6 150026088 150026088 single base substitution A G upstream_gene_variant LIRI-JP 6 150026423 150026423 single base substitution G C intron_variant LIRI-JP 6 150026423 150026423 single base substitution G C upstream_gene_variant LIRI-JP 6 150028081 150028081 single base substitution A G intron_variant LIRI-JP 6 150028081 150028081 single base substitution A G upstream_gene_variant LIRI-JP 6 150028425 150028425 single base substitution C T intron_variant LIRI-JP 6 150028425 150028425 single base substitution C T upstream_gene_variant LIRI-JP 6 150030590 150030590 single base substitution A G intron_variant LIRI-JP 6 150030634 150030634 single base substitution T C intron_variant LIRI-JP 6 150033114 150033114 single base substitution G A intron_variant LIRI-JP 6 150035988 150035988 single base substitution G T intron_variant LIRI-JP 6 150036455 150036455 single base substitution T C intron_variant LIRI-JP 6 150039698 150039698 single base substitution C A upstream_gene_variant LIRI-JP 6 150041075 150041075 single base substitution T C upstream_gene_variant LUSC-KR 6 149978821 149978821 single base substitution G A downstream_gene_variant LUSC-KR 6 149980133 149980133 single base substitution T C 3_prime_UTR_variant LUSC-KR 6 149980133 149980133 single base substitution T C downstream_gene_variant LUSC-KR 6 149987425 149987425 single base substitution C A intron_variant LUSC-KR 6 149989468 149989468 single base substitution C G intron_variant LUSC-KR 6 150004271 150004271 single base substitution T C 3_prime_UTR_variant LUSC-KR 6 150004271 150004271 single base substitution T C downstream_gene_variant LUSC-KR 6 150004271 150004271 single base substitution T C exon_variant LUSC-KR 6 150004271 150004271 single base substitution T C missense_variant K652E 1954A>G LUSC-KR 6 150008245 150008245 single base substitution G T intron_variant LUSC-KR 6 150011330 150011330 single base substitution T C intron_variant LUSC-KR 6 150028169 150028169 single base substitution G T intron_variant LUSC-KR 6 150028169 150028169 single base substitution G T upstream_gene_variant LUSC-KR 6 150030620 150030620 single base substitution G C intron_variant LUSC-US 6 149983278 149983278 single base substitution C T 3_prime_UTR_variant LUSC-US 6 149983278 149983278 single base substitution C T missense_variant D994N 2980G>A LUSC-US 6 149983369 149983369 single base substitution G A 3_prime_UTR_variant LUSC-US 6 149983369 149983369 single base substitution G A synonymous_variant I963I 2889C>T LUSC-US 6 150001043 150001043 single base substitution C T 3_prime_UTR_variant LUSC-US 6 150001043 150001043 single base substitution C T downstream_gene_variant LUSC-US 6 150001043 150001043 single base substitution C T exon_variant LUSC-US 6 150001043 150001043 single base substitution C T missense_variant R854K 2561G>A LUSC-US 6 150004302 150004302 single base substitution G A 3_prime_UTR_variant LUSC-US 6 150004302 150004302 single base substitution G A downstream_gene_variant LUSC-US 6 150004302 150004302 single base substitution G A exon_variant LUSC-US 6 150004302 150004302 single base substitution G A synonymous_variant F641F 1923C>T LUSC-US 6 150004707 150004707 single base substitution T C 3_prime_UTR_variant LUSC-US 6 150004707 150004707 single base substitution T C downstream_gene_variant LUSC-US 6 150004707 150004707 single base substitution T C exon_variant LUSC-US 6 150004707 150004707 single base substitution T C synonymous_variant P506P 1518A>G LUSC-US 6 150005649 150005649 single base substitution C A 3_prime_UTR_variant LUSC-US 6 150005649 150005649 single base substitution C A exon_variant LUSC-US 6 150005649 150005649 single base substitution C A synonymous_variant P138P 414G>T LUSC-US 6 150005649 150005649 single base substitution C A synonymous_variant P192P 576G>T LUSC-US 6 150023190 150023190 single base substitution C A exon_variant LUSC-US 6 150023190 150023190 single base substitution C A intron_variant LUSC-US 6 150023190 150023190 single base substitution C A missense_variant V25F 73G>T LUSC-US 6 150023190 150023190 single base substitution C A upstream_gene_variant MALY-DE 6 149977291 149977291 deletion of <=200bp G - downstream_gene_variant MALY-DE 6 149977295 149977297 deletion of <=200bp AAT - downstream_gene_variant MALY-DE 6 149984183 149984192 deletion of <=200bp AGACTACCTA - intron_variant MALY-DE 6 149987405 149987405 single base substitution A T intron_variant MALY-DE 6 149988975 149988975 insertion of <=200bp - T intron_variant MALY-DE 6 149989436 149989436 single base substitution T G intron_variant MALY-DE 6 149990865 149990865 single base substitution A G intron_variant MALY-DE 6 149994559 149994559 single base substitution T A downstream_gene_variant MALY-DE 6 149994559 149994559 single base substitution T A intron_variant MALY-DE 6 150006380 150006380 single base substitution A T intron_variant MALY-DE 6 150008227 150008227 single base substitution T G intron_variant MALY-DE 6 150013707 150013707 single base substitution C A intron_variant MALY-DE 6 150020358 150020358 single base substitution C T intron_variant MALY-DE 6 150026244 150026244 single base substitution T G intron_variant MALY-DE 6 150026244 150026244 single base substitution T G upstream_gene_variant MALY-DE 6 150034985 150034985 single base substitution G C intron_variant MALY-DE 6 150037221 150037221 single base substitution T A intron_variant MELA-AU 6 149974337 149974337 single base substitution G A downstream_gene_variant MELA-AU 6 149974643 149974643 single base substitution G A downstream_gene_variant MELA-AU 6 149974948 149974948 single base substitution C T downstream_gene_variant MELA-AU 6 149975304 149975304 single base substitution G T downstream_gene_variant MELA-AU 6 149976019 149976019 single base substitution G A downstream_gene_variant MELA-AU 6 149976911 149976911 single base substitution G A downstream_gene_variant MELA-AU 6 149977251 149977251 single base substitution G A downstream_gene_variant MELA-AU 6 149978088 149978088 single base substitution G A downstream_gene_variant MELA-AU 6 149978103 149978104 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 6 149978295 149978295 single base substitution G A downstream_gene_variant MELA-AU 6 149978453 149978453 single base substitution A G downstream_gene_variant MELA-AU 6 149980683 149980683 single base substitution G A 3_prime_UTR_variant MELA-AU 6 149980683 149980683 single base substitution G A downstream_gene_variant MELA-AU 6 149980768 149980768 single base substitution A C 3_prime_UTR_variant MELA-AU 6 149980768 149980768 single base substitution A C downstream_gene_variant MELA-AU 6 149980779 149980779 single base substitution G A 3_prime_UTR_variant MELA-AU 6 149980779 149980779 single base substitution G A downstream_gene_variant MELA-AU 6 149980933 149980933 single base substitution G A 3_prime_UTR_variant MELA-AU 6 149980933 149980933 single base substitution G A downstream_gene_variant MELA-AU 6 149981253 149981253 single base substitution C A 3_prime_UTR_variant MELA-AU 6 149981253 149981253 single base substitution C A downstream_gene_variant MELA-AU 6 149982732 149982732 single base substitution G A 3_prime_UTR_variant MELA-AU 6 149982732 149982732 single base substitution G A downstream_gene_variant MELA-AU 6 149983272 149983272 single base substitution A C 3_prime_UTR_variant MELA-AU 6 149983272 149983272 single base substitution A C missense_variant L996V 2986T>G MELA-AU 6 149983931 149983931 single base substitution C T intron_variant MELA-AU 6 149984220 149984220 single base substitution C T intron_variant MELA-AU 6 149984222 149984222 single base substitution T A intron_variant MELA-AU 6 149985622 149985622 single base substitution A G intron_variant MELA-AU 6 149986680 149986680 single base substitution G A intron_variant MELA-AU 6 149986712 149986712 single base substitution G A intron_variant MELA-AU 6 149986833 149986833 single base substitution G A intron_variant MELA-AU 6 149986876 149986876 single base substitution G A intron_variant MELA-AU 6 149987092 149987092 single base substitution A G intron_variant MELA-AU 6 149988175 149988175 single base substitution G A intron_variant MELA-AU 6 149988183 149988183 single base substitution A T intron_variant MELA-AU 6 149988452 149988452 single base substitution C G intron_variant MELA-AU 6 149988626 149988626 single base substitution A T intron_variant MELA-AU 6 149989218 149989218 single base substitution G A intron_variant MELA-AU 6 149989529 149989529 single base substitution G A intron_variant MELA-AU 6 149989851 149989851 single base substitution G A intron_variant MELA-AU 6 149989922 149989922 single base substitution A G intron_variant MELA-AU 6 149989974 149989974 single base substitution T A intron_variant MELA-AU 6 149990081 149990081 single base substitution G A intron_variant MELA-AU 6 149991234 149991234 single base substitution G A intron_variant MELA-AU 6 149992098 149992098 single base substitution G A downstream_gene_variant MELA-AU 6 149992098 149992098 single base substitution G A intron_variant MELA-AU 6 149992702 149992702 single base substitution T G downstream_gene_variant MELA-AU 6 149992702 149992702 single base substitution T G intron_variant MELA-AU 6 149992819 149992819 deletion of <=200bp A - downstream_gene_variant MELA-AU 6 149992819 149992819 deletion of <=200bp A - intron_variant MELA-AU 6 149993622 149993622 single base substitution G A downstream_gene_variant MELA-AU 6 149993622 149993622 single base substitution G A intron_variant MELA-AU 6 149993829 149993829 single base substitution C T downstream_gene_variant MELA-AU 6 149993829 149993829 single base substitution C T intron_variant MELA-AU 6 149993975 149993976 deletion of <=200bp GA - downstream_gene_variant MELA-AU 6 149993975 149993976 deletion of <=200bp GA - intron_variant MELA-AU 6 149994096 149994096 single base substitution G A downstream_gene_variant MELA-AU 6 149994096 149994096 single base substitution G A intron_variant MELA-AU 6 149994369 149994369 single base substitution G A downstream_gene_variant MELA-AU 6 149994369 149994369 single base substitution G A intron_variant MELA-AU 6 149994892 149994892 single base substitution C T downstream_gene_variant MELA-AU 6 149994892 149994892 single base substitution C T intron_variant MELA-AU 6 149995068 149995076 deletion of <=200bp CCCAAAGTG - downstream_gene_variant MELA-AU 6 149995068 149995076 deletion of <=200bp CCCAAAGTG - intron_variant MELA-AU 6 149996661 149996661 single base substitution G A downstream_gene_variant MELA-AU 6 149996661 149996661 single base substitution G A intron_variant MELA-AU 6 149997048 149997048 single base substitution G A exon_variant MELA-AU 6 149997048 149997048 single base substitution G A intron_variant MELA-AU 6 149998066 149998066 single base substitution G A intron_variant MELA-AU 6 149998142 149998142 single base substitution G A intron_variant MELA-AU 6 149998533 149998533 single base substitution G A intron_variant MELA-AU 6 149998699 149998699 single base substitution G A intron_variant MELA-AU 6 149998755 149998755 single base substitution A C intron_variant MELA-AU 6 149999217 149999217 single base substitution G A downstream_gene_variant MELA-AU 6 149999217 149999217 single base substitution G A intron_variant MELA-AU 6 149999556 149999556 single base substitution G A downstream_gene_variant MELA-AU 6 149999556 149999556 single base substitution G A intron_variant MELA-AU 6 149999909 149999909 single base substitution G A downstream_gene_variant MELA-AU 6 149999909 149999909 single base substitution G A intron_variant MELA-AU 6 150000195 150000195 single base substitution A T downstream_gene_variant MELA-AU 6 150000195 150000195 single base substitution A T intron_variant MELA-AU 6 150000619 150000619 single base substitution G A downstream_gene_variant MELA-AU 6 150000619 150000619 single base substitution G A intron_variant MELA-AU 6 150001535 150001535 single base substitution G A 3_prime_UTR_variant MELA-AU 6 150001535 150001535 single base substitution G A downstream_gene_variant MELA-AU 6 150001535 150001535 single base substitution G A exon_variant MELA-AU 6 150001535 150001535 single base substitution G A missense_variant S690F 2069C>T MELA-AU 6 150002496 150002496 single base substitution C T downstream_gene_variant MELA-AU 6 150002496 150002496 single base substitution C T intron_variant MELA-AU 6 150003611 150003611 single base substitution G A downstream_gene_variant MELA-AU 6 150003611 150003611 single base substitution G A intron_variant MELA-AU 6 150003996 150003996 single base substitution G A downstream_gene_variant MELA-AU 6 150003996 150003996 single base substitution G A intron_variant MELA-AU 6 150004011 150004011 single base substitution G A downstream_gene_variant MELA-AU 6 150004011 150004011 single base substitution G A intron_variant MELA-AU 6 150004522 150004522 single base substitution G A 3_prime_UTR_variant MELA-AU 6 150004522 150004522 single base substitution G A downstream_gene_variant MELA-AU 6 150004522 150004522 single base substitution G A exon_variant MELA-AU 6 150004522 150004522 single base substitution G A missense_variant P568L 1703C>T MELA-AU 6 150005204 150005204 single base substitution G A 3_prime_UTR_variant MELA-AU 6 150005204 150005204 single base substitution G A downstream_gene_variant MELA-AU 6 150005204 150005204 single base substitution G A exon_variant MELA-AU 6 150005204 150005204 single base substitution G A missense_variant P341S 1021C>T MELA-AU 6 150005370 150005370 single base substitution G A 3_prime_UTR_variant MELA-AU 6 150005370 150005370 single base substitution G A downstream_gene_variant MELA-AU 6 150005370 150005370 single base substitution G A exon_variant MELA-AU 6 150005370 150005370 single base substitution G A synonymous_variant I285I 855C>T MELA-AU 6 150006030 150006030 single base substitution T A intron_variant MELA-AU 6 150006790 150006790 single base substitution G A intron_variant MELA-AU 6 150008733 150008733 single base substitution T A intron_variant MELA-AU 6 150009910 150009910 single base substitution G A intron_variant MELA-AU 6 150011607 150011607 single base substitution C T intron_variant MELA-AU 6 150013834 150013834 single base substitution G A intron_variant MELA-AU 6 150014363 150014363 single base substitution A T intron_variant MELA-AU 6 150014748 150014755 deletion of <=200bp AAACAAAC - intron_variant MELA-AU 6 150015426 150015426 single base substitution A C intron_variant MELA-AU 6 150015941 150015941 single base substitution G A intron_variant MELA-AU 6 150016798 150016798 single base substitution G A intron_variant MELA-AU 6 150016837 150016837 single base substitution A T intron_variant MELA-AU 6 150017313 150017313 single base substitution G A intron_variant MELA-AU 6 150017686 150017686 single base substitution A G intron_variant MELA-AU 6 150018705 150018705 single base substitution A G intron_variant MELA-AU 6 150019596 150019596 single base substitution G A intron_variant MELA-AU 6 150021316 150021316 single base substitution A G intron_variant MELA-AU 6 150021731 150021731 single base substitution G A intron_variant MELA-AU 6 150022976 150022977 multiple base substitution (>=2bp and <=200bp) CG TA exon_variant MELA-AU 6 150022976 150022977 multiple base substitution (>=2bp and <=200bp) CG TA intron_variant MELA-AU 6 150022976 150022977 multiple base substitution (>=2bp and <=200bp) CG TA stop_gained R96* 286CG>TA MELA-AU 6 150023985 150023985 single base substitution A G intron_variant MELA-AU 6 150023985 150023985 single base substitution A G upstream_gene_variant MELA-AU 6 150024342 150024342 single base substitution C T intron_variant MELA-AU 6 150024342 150024342 single base substitution C T upstream_gene_variant MELA-AU 6 150025211 150025211 single base substitution C T intron_variant MELA-AU 6 150025211 150025211 single base substitution C T upstream_gene_variant MELA-AU 6 150025359 150025359 single base substitution G A intron_variant MELA-AU 6 150025359 150025359 single base substitution G A upstream_gene_variant MELA-AU 6 150026498 150026498 single base substitution A C intron_variant MELA-AU 6 150026498 150026498 single base substitution A C upstream_gene_variant MELA-AU 6 150027623 150027623 single base substitution G A intron_variant MELA-AU 6 150027623 150027623 single base substitution G A upstream_gene_variant MELA-AU 6 150028137 150028137 single base substitution C T intron_variant MELA-AU 6 150028137 150028137 single base substitution C T upstream_gene_variant MELA-AU 6 150028366 150028366 single base substitution G A intron_variant MELA-AU 6 150028366 150028366 single base substitution G A upstream_gene_variant MELA-AU 6 150029318 150029318 single base substitution A C intron_variant MELA-AU 6 150031519 150031519 single base substitution C T intron_variant MELA-AU 6 150032748 150032748 single base substitution T C intron_variant MELA-AU 6 150033076 150033076 single base substitution G T intron_variant MELA-AU 6 150033110 150033110 single base substitution G A intron_variant MELA-AU 6 150033523 150033523 single base substitution G A intron_variant MELA-AU 6 150033610 150033610 single base substitution G A intron_variant MELA-AU 6 150034901 150034901 single base substitution T C intron_variant MELA-AU 6 150035192 150035192 single base substitution C T intron_variant MELA-AU 6 150036728 150036728 single base substitution G A intron_variant MELA-AU 6 150036823 150036823 single base substitution G A intron_variant MELA-AU 6 150037008 150037008 single base substitution A T intron_variant MELA-AU 6 150039150 150039150 single base substitution G A 5_prime_UTR_variant MELA-AU 6 150039150 150039150 single base substitution G A synonymous_variant S7S 21C>T MELA-AU 6 150039150 150039150 single base substitution G A upstream_gene_variant MELA-AU 6 150039590 150039590 single base substitution G A upstream_gene_variant MELA-AU 6 150039780 150039780 single base substitution G A upstream_gene_variant MELA-AU 6 150040868 150040868 single base substitution C A upstream_gene_variant MELA-AU 6 150041500 150041500 single base substitution G A upstream_gene_variant MELA-AU 6 150042513 150042513 single base substitution C T upstream_gene_variant MELA-AU 6 150043319 150043319 single base substitution C A upstream_gene_variant MELA-AU 6 150043814 150043814 single base substitution C T upstream_gene_variant MELA-AU 6 150043935 150043935 single base substitution G A upstream_gene_variant MELA-AU 6 150044112 150044112 single base substitution C T upstream_gene_variant ORCA-IN 6 149986707 149986707 single base substitution G C intron_variant ORCA-IN 6 150032390 150032391 deletion of <=200bp AT - intron_variant ORCA-IN 6 150042097 150042097 single base substitution G A upstream_gene_variant OV-AU 6 149974869 149974869 single base substitution G A downstream_gene_variant OV-AU 6 149983268 149983268 single base substitution C A 3_prime_UTR_variant OV-AU 6 149983268 149983268 single base substitution C A missense_variant G997V 2990G>T OV-AU 6 149997715 149997715 single base substitution C A 3_prime_UTR_variant OV-AU 6 149997715 149997715 single base substitution C A exon_variant OV-AU 6 149997715 149997715 single base substitution C A missense_variant A918S 2752G>T OV-AU 6 150001061 150001061 single base substitution C A 3_prime_UTR_variant OV-AU 6 150001061 150001061 single base substitution C A downstream_gene_variant OV-AU 6 150001061 150001061 single base substitution C A exon_variant OV-AU 6 150001061 150001061 single base substitution C A missense_variant G848V 2543G>T OV-AU 6 150001329 150001329 single base substitution C T 3_prime_UTR_variant OV-AU 6 150001329 150001329 single base substitution C T downstream_gene_variant OV-AU 6 150001329 150001329 single base substitution C T exon_variant OV-AU 6 150001329 150001329 single base substitution C T missense_variant E759K 2275G>A OV-AU 6 150001623 150001623 single base substitution A G downstream_gene_variant OV-AU 6 150001623 150001623 single base substitution A G intron_variant OV-AU 6 150014683 150014683 single base substitution T C intron_variant OV-AU 6 150019566 150019566 single base substitution G C intron_variant OV-AU 6 150026734 150026734 single base substitution G A intron_variant OV-AU 6 150026734 150026734 single base substitution G A upstream_gene_variant OV-AU 6 150041565 150041565 single base substitution T A upstream_gene_variant OV-US 6 150004239 150004239 single base substitution T C 3_prime_UTR_variant OV-US 6 150004239 150004239 single base substitution T C downstream_gene_variant OV-US 6 150004239 150004239 single base substitution T C exon_variant OV-US 6 150004239 150004239 single base substitution T C synonymous_variant K662K 1986A>G OV-US 6 150004708 150004708 single base substitution G C 3_prime_UTR_variant OV-US 6 150004708 150004708 single base substitution G C downstream_gene_variant OV-US 6 150004708 150004708 single base substitution G C exon_variant OV-US 6 150004708 150004708 single base substitution G C missense_variant P506R 1517C>G PACA-AU 6 149976736 149976736 single base substitution G A downstream_gene_variant PACA-AU 6 149979294 149979294 single base substitution A C 3_prime_UTR_variant PACA-AU 6 149979294 149979294 single base substitution A C downstream_gene_variant PACA-AU 6 149980865 149980865 single base substitution C T 3_prime_UTR_variant PACA-AU 6 149980865 149980865 single base substitution C T downstream_gene_variant PACA-AU 6 149983094 149983094 single base substitution T G 3_prime_UTR_variant PACA-AU 6 149983094 149983094 single base substitution T G missense_variant E1055A 3164A>C PACA-AU 6 149983363 149983363 single base substitution C A 3_prime_UTR_variant PACA-AU 6 149983363 149983363 single base substitution C A missense_variant W965C 2895G>T PACA-AU 6 149987370 149987382 deletion of <=200bp AAACAAAAAACAA - intron_variant PACA-AU 6 149991074 149991074 single base substitution G A intron_variant PACA-AU 6 149994478 149994478 single base substitution A C downstream_gene_variant PACA-AU 6 149994478 149994478 single base substitution A C intron_variant PACA-AU 6 149996794 149996794 single base substitution G C downstream_gene_variant PACA-AU 6 149996794 149996794 single base substitution G C intron_variant PACA-AU 6 149999601 149999601 single base substitution T C downstream_gene_variant PACA-AU 6 149999601 149999601 single base substitution T C intron_variant PACA-AU 6 150000946 150000946 single base substitution T G downstream_gene_variant PACA-AU 6 150000946 150000946 single base substitution T G intron_variant PACA-AU 6 150004475 150004475 single base substitution G A 3_prime_UTR_variant PACA-AU 6 150004475 150004475 single base substitution G A downstream_gene_variant PACA-AU 6 150004475 150004475 single base substitution G A exon_variant PACA-AU 6 150004475 150004475 single base substitution G A stop_gained Q584* 1750C>T PACA-AU 6 150004887 150004887 single base substitution G C 3_prime_UTR_variant PACA-AU 6 150004887 150004887 single base substitution G C downstream_gene_variant PACA-AU 6 150004887 150004887 single base substitution G C exon_variant PACA-AU 6 150004887 150004887 single base substitution G C missense_variant S446R 1338C>G PACA-AU 6 150009687 150009687 single base substitution G A intron_variant PACA-AU 6 150014953 150014953 single base substitution C T intron_variant PACA-AU 6 150016377 150016377 single base substitution A T intron_variant PACA-AU 6 150018132 150018132 single base substitution C T intron_variant PACA-AU 6 150018322 150018322 single base substitution C T intron_variant PACA-AU 6 150018322 150018322 single base substitution C T splice_region_variant PACA-AU 6 150026721 150026721 insertion of <=200bp - AG intron_variant PACA-AU 6 150026721 150026721 insertion of <=200bp - AG upstream_gene_variant PACA-AU 6 150036308 150036308 single base substitution G A intron_variant PACA-AU 6 150038727 150038727 single base substitution G T intron_variant PACA-AU 6 150038727 150038727 single base substitution G T upstream_gene_variant PACA-AU 6 150038803 150038803 single base substitution C T intron_variant PACA-AU 6 150038803 150038803 single base substitution C T upstream_gene_variant PACA-AU 6 150038808 150038808 single base substitution C G intron_variant PACA-AU 6 150038808 150038808 single base substitution C G upstream_gene_variant PACA-CA 6 149975651 149975651 insertion of <=200bp - A downstream_gene_variant PACA-CA 6 149975766 149975766 single base substitution G C downstream_gene_variant PACA-CA 6 149981613 149981613 single base substitution C T 3_prime_UTR_variant PACA-CA 6 149981613 149981613 single base substitution C T downstream_gene_variant PACA-CA 6 149985122 149985122 single base substitution T C intron_variant PACA-CA 6 149985863 149985863 single base substitution T A intron_variant PACA-CA 6 149992308 149992308 single base substitution A G downstream_gene_variant PACA-CA 6 149992308 149992308 single base substitution A G intron_variant PACA-CA 6 149992376 149992376 single base substitution C T downstream_gene_variant PACA-CA 6 149992376 149992376 single base substitution C T intron_variant PACA-CA 6 149994083 149994083 single base substitution A G downstream_gene_variant PACA-CA 6 149994083 149994083 single base substitution A G intron_variant PACA-CA 6 149998173 149998173 single base substitution C T intron_variant PACA-CA 6 150009230 150009230 single base substitution C T intron_variant PACA-CA 6 150015527 150015527 single base substitution G C intron_variant PACA-CA 6 150018321 150018321 single base substitution T C intron_variant PACA-CA 6 150018321 150018321 single base substitution T C splice_region_variant PACA-CA 6 150020618 150020618 single base substitution A T intron_variant PACA-CA 6 150020751 150020751 single base substitution T C intron_variant PACA-CA 6 150022695 150022716 deletion of <=200bp CAGAATTTAGTGATACATATCA - intron_variant PACA-CA 6 150023206 150023206 insertion of <=200bp - G exon_variant PACA-CA 6 150023206 150023206 insertion of <=200bp - G frameshift_variant P19P? PACA-CA 6 150023206 150023206 insertion of <=200bp - G intron_variant PACA-CA 6 150023206 150023206 insertion of <=200bp - G upstream_gene_variant PACA-CA 6 150027661 150027661 single base substitution T C intron_variant PACA-CA 6 150027661 150027661 single base substitution T C upstream_gene_variant PACA-CA 6 150028619 150028619 single base substitution A C intron_variant PACA-CA 6 150032389 150032389 single base substitution A T intron_variant PACA-CA 6 150039458 150039458 single base substitution C A upstream_gene_variant PACA-CA 6 150042679 150042679 single base substitution C T upstream_gene_variant PACA-CA 6 150043581 150043581 single base substitution G C upstream_gene_variant PACA-CA 6 150043836 150043836 single base substitution A C upstream_gene_variant PAEN-IT 6 149974902 149974902 single base substitution G T downstream_gene_variant PAEN-IT 6 149986617 149986617 single base substitution T C intron_variant PBCA-DE 6 149975539 149975539 single base substitution G A downstream_gene_variant PBCA-DE 6 149977960 149977960 single base substitution G A downstream_gene_variant PBCA-DE 6 149994409 149994409 insertion of <=200bp - T downstream_gene_variant PBCA-DE 6 149994409 149994409 insertion of <=200bp - T intron_variant PBCA-DE 6 149995907 149995907 deletion of <=200bp A - downstream_gene_variant PBCA-DE 6 149995907 149995907 deletion of <=200bp A - intron_variant PBCA-DE 6 150006940 150006940 deletion of <=200bp A - intron_variant PBCA-DE 6 150024549 150024549 single base substitution A G intron_variant PBCA-DE 6 150024549 150024549 single base substitution A G upstream_gene_variant PBCA-DE 6 150030026 150030026 single base substitution C T intron_variant PBCA-DE 6 150037185 150037185 deletion of <=200bp T - intron_variant PRAD-CA 6 150012180 150012180 single base substitution C A intron_variant PRAD-CA 6 150024082 150024082 single base substitution T A intron_variant PRAD-CA 6 150024082 150024082 single base substitution T A upstream_gene_variant PRAD-CA 6 150033718 150033718 single base substitution C G intron_variant PRAD-UK 6 149981798 149981798 single base substitution G A 3_prime_UTR_variant PRAD-UK 6 149981798 149981798 single base substitution G A downstream_gene_variant PRAD-UK 6 149983491 149983491 single base substitution A G intron_variant PRAD-UK 6 149995400 149995400 single base substitution A G downstream_gene_variant PRAD-UK 6 149995400 149995400 single base substitution A G intron_variant PRAD-UK 6 149995409 149995409 single base substitution C A downstream_gene_variant PRAD-UK 6 149995409 149995409 single base substitution C A intron_variant PRAD-UK 6 150024838 150024843 deletion of <=200bp AAAAAA - intron_variant PRAD-UK 6 150024838 150024843 deletion of <=200bp AAAAAA - upstream_gene_variant PRAD-UK 6 150037812 150037812 single base substitution T A intron_variant PRAD-UK 6 150037812 150037812 single base substitution T A upstream_gene_variant READ-US 6 149983274 149983274 single base substitution C T 3_prime_UTR_variant READ-US 6 149983274 149983274 single base substitution C T missense_variant R995H 2984G>A READ-US 6 150004506 150004506 single base substitution G A 3_prime_UTR_variant READ-US 6 150004506 150004506 single base substitution G A downstream_gene_variant READ-US 6 150004506 150004506 single base substitution G A exon_variant READ-US 6 150004506 150004506 single base substitution G A synonymous_variant Y573Y 1719C>T READ-US 6 150005395 150005395 single base substitution T C 3_prime_UTR_variant READ-US 6 150005395 150005395 single base substitution T C downstream_gene_variant READ-US 6 150005395 150005395 single base substitution T C exon_variant READ-US 6 150005395 150005395 single base substitution T C missense_variant Y277C 830A>G READ-US 6 150023019 150023019 single base substitution G A exon_variant READ-US 6 150023019 150023019 single base substitution G A intron_variant READ-US 6 150023019 150023019 single base substitution G A stop_gained R82* 244C>T RECA-EU 6 149974300 149974300 single base substitution C A downstream_gene_variant RECA-EU 6 149974796 149974796 single base substitution A G downstream_gene_variant RECA-EU 6 149975997 149975997 single base substitution G A downstream_gene_variant RECA-EU 6 149979407 149979407 single base substitution G A 3_prime_UTR_variant RECA-EU 6 149979407 149979407 single base substitution G A downstream_gene_variant RECA-EU 6 149984256 149984256 single base substitution C T intron_variant RECA-EU 6 149999038 149999038 single base substitution T G intron_variant RECA-EU 6 150017879 150017879 single base substitution G T intron_variant RECA-EU 6 150022147 150022147 single base substitution G A intron_variant RECA-EU 6 150022149 150022149 single base substitution C T intron_variant RECA-EU 6 150022408 150022408 single base substitution T A intron_variant RECA-EU 6 150027573 150027573 single base substitution G C intron_variant RECA-EU 6 150027573 150027573 single base substitution G C upstream_gene_variant RECA-EU 6 150028152 150028152 single base substitution T C intron_variant RECA-EU 6 150028152 150028152 single base substitution T C upstream_gene_variant RECA-EU 6 150030262 150030262 single base substitution C A intron_variant RECA-EU 6 150038232 150038232 single base substitution A G intron_variant RECA-EU 6 150038232 150038232 single base substitution A G upstream_gene_variant RECA-EU 6 150042716 150042716 single base substitution G T upstream_gene_variant SKCA-BR 6 149975572 149975572 single base substitution G A downstream_gene_variant SKCA-BR 6 149978758 149978758 single base substitution T A downstream_gene_variant SKCA-BR 6 149979349 149979349 single base substitution G A 3_prime_UTR_variant SKCA-BR 6 149979349 149979349 single base substitution G A downstream_gene_variant SKCA-BR 6 149980523 149980523 single base substitution A C 3_prime_UTR_variant SKCA-BR 6 149980523 149980523 single base substitution A C downstream_gene_variant SKCA-BR 6 149980571 149980571 single base substitution G A 3_prime_UTR_variant SKCA-BR 6 149980571 149980571 single base substitution G A downstream_gene_variant SKCA-BR 6 149984130 149984130 single base substitution T A intron_variant SKCA-BR 6 149985297 149985298 deletion of <=200bp CA - intron_variant SKCA-BR 6 149988079 149988079 insertion of <=200bp - CA intron_variant SKCA-BR 6 149989744 149989745 deletion of <=200bp AT - intron_variant SKCA-BR 6 149991326 149991330 deletion of <=200bp AAAAG - intron_variant SKCA-BR 6 149991330 149991330 single base substitution G A intron_variant SKCA-BR 6 149996351 149996352 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 6 149996351 149996352 deletion of <=200bp CA - intron_variant SKCA-BR 6 150002686 150002686 single base substitution G A downstream_gene_variant SKCA-BR 6 150002686 150002686 single base substitution G A intron_variant SKCA-BR 6 150004104 150004104 single base substitution A G 3_prime_UTR_variant SKCA-BR 6 150004104 150004104 single base substitution A G downstream_gene_variant SKCA-BR 6 150004104 150004104 single base substitution A G intron_variant SKCA-BR 6 150011107 150011107 insertion of <=200bp - TA intron_variant SKCA-BR 6 150012478 150012478 single base substitution A C intron_variant SKCA-BR 6 150013813 150013813 insertion of <=200bp - CT intron_variant SKCA-BR 6 150017103 150017103 single base substitution C T intron_variant SKCA-BR 6 150017723 150017723 single base substitution G A intron_variant SKCA-BR 6 150017778 150017778 single base substitution C T intron_variant SKCA-BR 6 150019618 150019618 single base substitution G A intron_variant SKCA-BR 6 150019674 150019674 single base substitution A C intron_variant SKCA-BR 6 150027600 150027600 single base substitution T A intron_variant SKCA-BR 6 150027600 150027600 single base substitution T A upstream_gene_variant SKCA-BR 6 150027601 150027601 single base substitution G A intron_variant SKCA-BR 6 150027601 150027601 single base substitution G A upstream_gene_variant SKCA-BR 6 150028338 150028338 single base substitution G A intron_variant SKCA-BR 6 150028338 150028338 single base substitution G A upstream_gene_variant SKCA-BR 6 150030136 150030136 single base substitution G A intron_variant SKCA-BR 6 150033941 150033941 single base substitution G A intron_variant SKCA-BR 6 150039085 150039085 single base substitution G T 5_prime_UTR_variant SKCA-BR 6 150039085 150039085 single base substitution G T missense_variant P29H 86C>A SKCA-BR 6 150039085 150039085 single base substitution G T upstream_gene_variant SKCA-BR 6 150043855 150043855 single base substitution G A upstream_gene_variant SKCM-US 6 149983316 149983316 single base substitution G A 3_prime_UTR_variant SKCM-US 6 149983316 149983316 single base substitution G A missense_variant A981V 2942C>T SKCM-US 6 150004522 150004522 single base substitution G A 3_prime_UTR_variant SKCM-US 6 150004522 150004522 single base substitution G A downstream_gene_variant SKCM-US 6 150004522 150004522 single base substitution G A exon_variant SKCM-US 6 150004522 150004522 single base substitution G A missense_variant P568L 1703C>T SKCM-US 6 150005324 150005324 single base substitution G A 3_prime_UTR_variant SKCM-US 6 150005324 150005324 single base substitution G A downstream_gene_variant SKCM-US 6 150005324 150005324 single base substitution G A exon_variant SKCM-US 6 150005324 150005324 single base substitution G A missense_variant P301S 901C>T SKCM-US 6 150005350 150005350 single base substitution G A 3_prime_UTR_variant SKCM-US 6 150005350 150005350 single base substitution G A downstream_gene_variant SKCM-US 6 150005350 150005350 single base substitution G A exon_variant SKCM-US 6 150005350 150005350 single base substitution G A missense_variant P292L 875C>T SKCM-US 6 150005421 150005421 single base substitution C T 3_prime_UTR_variant SKCM-US 6 150005421 150005421 single base substitution C T downstream_gene_variant SKCM-US 6 150005421 150005421 single base substitution C T exon_variant SKCM-US 6 150005421 150005421 single base substitution C T stop_gained W268* 804G>A SKCM-US 6 150022976 150022976 single base substitution C T exon_variant SKCM-US 6 150022976 150022976 single base substitution C T intron_variant SKCM-US 6 150022976 150022976 single base substitution C T missense_variant R96Q 287G>A STAD-US 6 149983002 149983002 single base substitution C A 3_prime_UTR_variant STAD-US 6 149983002 149983002 single base substitution C A missense_variant D1086Y 3256G>T STAD-US 6 149983013 149983013 single base substitution C T 3_prime_UTR_variant STAD-US 6 149983013 149983013 single base substitution C T missense_variant R1082K 3245G>A STAD-US 6 149983146 149983146 single base substitution T G 3_prime_UTR_variant STAD-US 6 149983146 149983146 single base substitution T G missense_variant N1038H 3112A>C STAD-US 6 149983213 149983213 single base substitution G T 3_prime_UTR_variant STAD-US 6 149983213 149983213 single base substitution G T missense_variant F1015L 3045C>A STAD-US 6 150001244 150001244 single base substitution C G 3_prime_UTR_variant STAD-US 6 150001244 150001244 single base substitution C G downstream_gene_variant STAD-US 6 150001244 150001244 single base substitution C G exon_variant STAD-US 6 150001244 150001244 single base substitution C G missense_variant G787A 2360G>C STAD-US 6 150001426 150001426 single base substitution A G 3_prime_UTR_variant STAD-US 6 150001426 150001426 single base substitution A G downstream_gene_variant STAD-US 6 150001426 150001426 single base substitution A G exon_variant STAD-US 6 150001426 150001426 single base substitution A G synonymous_variant D726D 2178T>C STAD-US 6 150001447 150001447 single base substitution G A 3_prime_UTR_variant STAD-US 6 150001447 150001447 single base substitution G A downstream_gene_variant STAD-US 6 150001447 150001447 single base substitution G A exon_variant STAD-US 6 150001447 150001447 single base substitution G A synonymous_variant V719V 2157C>T STAD-US 6 150001570 150001570 single base substitution C A 3_prime_UTR_variant STAD-US 6 150001570 150001570 single base substitution C A downstream_gene_variant STAD-US 6 150001570 150001570 single base substitution C A exon_variant STAD-US 6 150001570 150001570 single base substitution C A missense_variant Q678H 2034G>T STAD-US 6 150004383 150004383 single base substitution A G 3_prime_UTR_variant STAD-US 6 150004383 150004383 single base substitution A G downstream_gene_variant STAD-US 6 150004383 150004383 single base substitution A G exon_variant STAD-US 6 150004383 150004383 single base substitution A G synonymous_variant P614P 1842T>C STAD-US 6 150004573 150004573 single base substitution T C 3_prime_UTR_variant STAD-US 6 150004573 150004573 single base substitution T C downstream_gene_variant STAD-US 6 150004573 150004573 single base substitution T C exon_variant STAD-US 6 150004573 150004573 single base substitution T C missense_variant N551S 1652A>G STAD-US 6 150004580 150004580 single base substitution C A 3_prime_UTR_variant STAD-US 6 150004580 150004580 single base substitution C A downstream_gene_variant STAD-US 6 150004580 150004580 single base substitution C A exon_variant STAD-US 6 150004580 150004580 single base substitution C A missense_variant A549S 1645G>T STAD-US 6 150004716 150004716 single base substitution T C 3_prime_UTR_variant STAD-US 6 150004716 150004716 single base substitution T C downstream_gene_variant STAD-US 6 150004716 150004716 single base substitution T C exon_variant STAD-US 6 150004716 150004716 single base substitution T C synonymous_variant V503V 1509A>G STAD-US 6 150004778 150004778 single base substitution C T 3_prime_UTR_variant STAD-US 6 150004778 150004778 single base substitution C T downstream_gene_variant STAD-US 6 150004778 150004778 single base substitution C T exon_variant STAD-US 6 150004778 150004778 single base substitution C T missense_variant A483T 1447G>A STAD-US 6 150004891 150004891 single base substitution G A 3_prime_UTR_variant STAD-US 6 150004891 150004891 single base substitution G A downstream_gene_variant STAD-US 6 150004891 150004891 single base substitution G A exon_variant STAD-US 6 150004891 150004891 single base substitution G A missense_variant P445L 1334C>T STAD-US 6 150004895 150004895 single base substitution A G 3_prime_UTR_variant STAD-US 6 150004895 150004895 single base substitution A G downstream_gene_variant STAD-US 6 150004895 150004895 single base substitution A G exon_variant STAD-US 6 150004895 150004895 single base substitution A G missense_variant S444P 1330T>C STAD-US 6 150005125 150005125 single base substitution G A 3_prime_UTR_variant STAD-US 6 150005125 150005125 single base substitution G A downstream_gene_variant STAD-US 6 150005125 150005125 single base substitution G A exon_variant STAD-US 6 150005125 150005125 single base substitution G A missense_variant T367I 1100C>T STAD-US 6 150005455 150005455 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 6 150005455 150005455 deletion of <=200bp G - downstream_gene_variant STAD-US 6 150005455 150005455 deletion of <=200bp G - exon_variant STAD-US 6 150005455 150005455 deletion of <=200bp G - frameshift_variant P257 STAD-US 6 150005576 150005579 deletion of <=200bp CAGA - 3_prime_UTR_variant STAD-US 6 150005576 150005579 deletion of <=200bp CAGA - exon_variant STAD-US 6 150005576 150005579 deletion of <=200bp CAGA - frameshift_variant SG162 STAD-US 6 150005576 150005579 deletion of <=200bp CAGA - frameshift_variant SG216 STAD-US 6 150005721 150005721 single base substitution C T 3_prime_UTR_variant STAD-US 6 150005721 150005721 single base substitution C T exon_variant STAD-US 6 150005721 150005721 single base substitution C T synonymous_variant V114V 342G>A STAD-US 6 150005721 150005721 single base substitution C T synonymous_variant V168V 504G>A STAD-US 6 150016224 150016224 single base substitution G A 3_prime_UTR_variant STAD-US 6 150016224 150016224 single base substitution G A exon_variant STAD-US 6 150016224 150016224 single base substitution G A missense_variant A107V 320C>T STAD-US 6 150016224 150016224 single base substitution G A missense_variant A161V 482C>T STAD-US 6 150016247 150016247 single base substitution T A 3_prime_UTR_variant STAD-US 6 150016247 150016247 single base substitution T A exon_variant STAD-US 6 150016247 150016247 single base substitution T A synonymous_variant A153A 459A>T STAD-US 6 150016247 150016247 single base substitution T A synonymous_variant A99A 297A>T STAD-US 6 150023018 150023018 single base substitution C T exon_variant STAD-US 6 150023018 150023018 single base substitution C T intron_variant STAD-US 6 150023018 150023018 single base substitution C T missense_variant R82Q 245G>A STAD-US 6 150023031 150023031 single base substitution A G exon_variant STAD-US 6 150023031 150023031 single base substitution A G intron_variant STAD-US 6 150023031 150023031 single base substitution A G synonymous_variant L78L 232T>C THCA-SA 6 149982417 149982417 single base substitution A G 3_prime_UTR_variant THCA-SA 6 149982417 149982417 single base substitution A G downstream_gene_variant THCA-SA 6 149983216 149983216 single base substitution G A 3_prime_UTR_variant THCA-SA 6 149983216 149983216 single base substitution G A synonymous_variant D1014D 3042C>T THCA-SA 6 150004779 150004779 single base substitution A G 3_prime_UTR_variant THCA-SA 6 150004779 150004779 single base substitution A G downstream_gene_variant THCA-SA 6 150004779 150004779 single base substitution A G exon_variant THCA-SA 6 150004779 150004779 single base substitution A G synonymous_variant S482S 1446T>C THCA-SA 6 150023348 150023348 single base substitution C G 5_prime_UTR_variant THCA-SA 6 150023348 150023348 single base substitution C G intron_variant THCA-SA 6 150023348 150023348 single base substitution C G upstream_gene_variant THCA-SA 6 150039148 150039148 single base substitution G A 5_prime_UTR_variant THCA-SA 6 150039148 150039148 single base substitution G A missense_variant S8L 23C>T THCA-SA 6 150039148 150039148 single base substitution G A upstream_gene_variant THCA-SA 6 150039293 150039293 single base substitution T C 5_prime_UTR_variant THCA-SA 6 150039293 150039293 single base substitution T C upstream_gene_variant THCA-SA 6 150039361 150039361 single base substitution C G 5_prime_UTR_variant THCA-SA 6 150039361 150039361 single base substitution C G upstream_gene_variant UCEC-US 6 149997763 149997772 deletion of <=200bp GCTGGCGTGC - 3_prime_UTR_variant UCEC-US 6 149997763 149997772 deletion of <=200bp GCTGGCGTGC - exon_variant UCEC-US 6 149997763 149997772 deletion of <=200bp GCTGGCGTGC - frameshift_variant ARQH899 UCEC-US 6 149997856 149997856 single base substitution C A 3_prime_UTR_variant UCEC-US 6 149997856 149997856 single base substitution C A exon_variant UCEC-US 6 149997856 149997856 single base substitution C A missense_variant D871Y 2611G>T UCEC-US 6 150001374 150001374 single base substitution G A 3_prime_UTR_variant UCEC-US 6 150001374 150001374 single base substitution G A downstream_gene_variant UCEC-US 6 150001374 150001374 single base substitution G A exon_variant UCEC-US 6 150001374 150001374 single base substitution G A stop_gained R744* 2230C>T UCEC-US 6 150001395 150001395 single base substitution G A 3_prime_UTR_variant UCEC-US 6 150001395 150001395 single base substitution G A downstream_gene_variant UCEC-US 6 150001395 150001395 single base substitution G A exon_variant UCEC-US 6 150001395 150001395 single base substitution G A stop_gained R737* 2209C>T UCEC-US 6 150004256 150004256 single base substitution G A 3_prime_UTR_variant UCEC-US 6 150004256 150004256 single base substitution G A downstream_gene_variant UCEC-US 6 150004256 150004256 single base substitution G A exon_variant UCEC-US 6 150004256 150004256 single base substitution G A missense_variant R657C 1969C>T UCEC-US 6 150004302 150004302 single base substitution G T 3_prime_UTR_variant UCEC-US 6 150004302 150004302 single base substitution G T downstream_gene_variant UCEC-US 6 150004302 150004302 single base substitution G T exon_variant UCEC-US 6 150004302 150004302 single base substitution G T missense_variant F641L 1923C>A UCEC-US 6 150004404 150004404 single base substitution C A 3_prime_UTR_variant UCEC-US 6 150004404 150004404 single base substitution C A downstream_gene_variant UCEC-US 6 150004404 150004404 single base substitution C A exon_variant UCEC-US 6 150004404 150004404 single base substitution C A missense_variant K607N 1821G>T UCEC-US 6 150004490 150004490 single base substitution G A 3_prime_UTR_variant UCEC-US 6 150004490 150004490 single base substitution G A downstream_gene_variant UCEC-US 6 150004490 150004490 single base substitution G A exon_variant UCEC-US 6 150004490 150004490 single base substitution G A missense_variant P579S 1735C>T UCEC-US 6 150005070 150005070 single base substitution G A 3_prime_UTR_variant UCEC-US 6 150005070 150005070 single base substitution G A downstream_gene_variant UCEC-US 6 150005070 150005070 single base substitution G A exon_variant UCEC-US 6 150005070 150005070 single base substitution G A synonymous_variant S385S 1155C>T UCEC-US 6 150005526 150005526 single base substitution T G 3_prime_UTR_variant UCEC-US 6 150005526 150005526 single base substitution T G downstream_gene_variant UCEC-US 6 150005526 150005526 single base substitution T G exon_variant UCEC-US 6 150005526 150005526 single base substitution T G missense_variant R179S 537A>C UCEC-US 6 150005526 150005526 single base substitution T G missense_variant R233S 699A>C UCEC-US 6 150022965 150022965 single base substitution C A exon_variant UCEC-US 6 150022965 150022965 single base substitution C A intron_variant UCEC-US 6 150022965 150022965 single base substitution C A stop_gained E100* 298G>T UCEC-US 6 150023019 150023019 single base substitution G A exon_variant UCEC-US 6 150023019 150023019 single base substitution G A intron_variant UCEC-US 6 150023019 150023019 single base substitution G A stop_gained R82* 244C>T UCEC-US 6 150023129 150023129 single base substitution G T exon_variant UCEC-US 6 150023129 150023129 single base substitution G T intron_variant UCEC-US 6 150023129 150023129 single base substitution G T missense_variant S45Y 134C>A UCEC-US 6 150023129 150023129 single base substitution G T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BP-4989-01 COSM483526 c.1661G>A p.G554E Substitution - Missense 6:149683428-149683428 - HCC159T COSM3662038 c.2648C>G p.S883* Substitution - Nonsense 6:149676683-149676683 - TCGA-AX-A063-01 COSM1074457 c.1735C>T p.P579S Substitution - Missense 6:149683354-149683354 - 2521259 COSM5869494 c.2656C>T p.R886* Substitution - Nonsense 6:149676675-149676675 - B109 COSM1754589 c.338G>A p.G113E Substitution - Missense 6:149701789-149701789 - I2L-P19Ta-Tumor-Biopsy COSM5357280 c.2234A>G p.N745S Substitution - Missense 6:149680234-149680234 - TCGA-13-1489-01 COSM4947519 c.1986A>G p.K662K Substitution - coding silent 6:149683103-149683103 - PD3945a COSM219259 c.3346C>G p.Q1116E Substitution - Missense 6:149661776-149661776 - TCGA-BS-A0UV-01 COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - C135 COSM4618573 c.3156C>T p.N1052N Substitution - coding silent 6:149661966-149661966 - HX13T COSM1621052 c.175A>G p.T59A Substitution - Missense 6:149701952-149701952 - TCGA-AM-5821-01 COSM3761536 c.975T>C p.V325V Substitution - coding silent 6:149684114-149684114 - TCGA-CD-A4MJ-01 COSM3859026 c.1447G>A p.A483T Substitution - Missense 6:149683642-149683642 - TCGA-BR-4280-01 COSM3018707 c.3245G>A p.R1082K Substitution - Missense 6:149661877-149661877 - TCGA-A5-A0G9-01 COSM1074451 c.1969C>T p.R657C Substitution - Missense 6:149683120-149683120 - TCGA-A8-A07R-01 COSM450665 c.3082C>G p.P1028A Substitution - Missense 6:149662040-149662040 - TCGA-AC-A23H-01 COSM3829277 c.2512C>G p.R838G Substitution - Missense 6:149679956-149679956 - ESCC_BICR_049T COSM5433342 c.2434C>T p.L812F Substitution - Missense 6:149680034-149680034 - PT43 COSM5943882 c.2884-12_2887del16 p.? Unknown 6:149662235-149662250 - HCT116 COSM3018782 c.1596delT p.P533fs*8 Deletion - Frameshift 6:149683493-149683493 - TCGA-AM-5821-01 COSM3761531 c.3042C>T p.D1014D Substitution - coding silent 6:149662080-149662080 - HCT15 COSM1672832 c.2552C>T p.T851I Substitution - Missense 6:149679916-149679916 - KM12 COSM3018826 c.326T>C p.L109S Substitution - Missense 6:149701801-149701801 - pfg052T COSM4762512 c.2481A>T p.R827S Substitution - Missense 6:149679987-149679987 - Pat_26_B COSM5869494 c.2656C>T p.R886* Substitution - Nonsense 6:149676675-149676675 - TCGA-B5-A0JY-01 COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - TCGA-CF-A1HR-01 COSM421036 c.864C>G p.I288M Substitution - Missense 6:149684225-149684225 - TCGA-AD-6889-01 COSM1441120 c.2416C>T p.R806* Substitution - Nonsense 6:149680052-149680052 - TCGA-66-2767-01 COSM740639 c.576G>T p.P192P Substitution - coding silent 6:149684513-149684513 - DLD1 COSM1672832 c.2552C>T p.T851I Substitution - Missense 6:149679916-149679916 - CSCC-1-T COSM4451396 c.119A>G p.N40S Substitution - Missense 6:149702008-149702008 - Au1 COSM5596968 c.897C>T p.G299G Substitution - coding silent 6:149684192-149684192 - PT51 COSM5938150 c.445G>A p.E149K Substitution - Missense 6:149695125-149695125 - HCC4 COSM1621052 c.175A>G p.T59A Substitution - Missense 6:149701952-149701952 - TCGA-P4-A5EB-01 COSM3994647 c.2640G>C p.G880G Substitution - coding silent 6:149676691-149676691 - TCGA-BR-8591-01 COSM3859010 c.2157C>T p.V719V Substitution - coding silent 6:149680311-149680311 - CSCC-16-T COSM4456146 c.2349_2350CT>AC p.D783_Y784>EH Complex - compound substitution 6:149680118-149680119 - 8069060 COSM3781579 c.2895G>T p.W965C Substitution - Missense 6:149662227-149662227 - TCGA-D3-A51R-06 COSM3621398 c.875C>T p.P292L Substitution - Missense 6:149684214-149684214 - TCGA-BP-4992-01 COSM483528 c.1323C>T p.A441A Substitution - coding silent 6:149683766-149683766 - TCGA-FP-7829-01 COSM3859035 c.1100C>T p.T367I Substitution - Missense 6:149683989-149683989 - LOXIMVI COSM1672830 c.2984G>T p.R995L Substitution - Missense 6:149662138-149662138 - 2521262 COSM5891933 c.877C>T p.P293S Substitution - Missense 6:149684212-149684212 - TCGA-BR-8384-01 COSM3859006 c.2360G>C p.G787A Substitution - Missense 6:149680108-149680108 - TCGA-A5-A0G9-01 COSM1074447 c.2530T>A p.L844M Substitution - Missense 6:149679938-149679938 - TCGA-EI-6917-01 COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - TCGA-Q1-A73O-01 COSM4836249 c.2118G>T p.V706V Substitution - coding silent 6:149680350-149680350 - 71 COSM5014653 c.2002A>G p.M668V Substitution - Missense 6:149683087-149683087 - 3402_T COSM3948148 c.2011-2A>C p.? Unknown 6:149680459-149680459 - 2290929 COSM4440058 c.3286C>T p.P1096S Substitution - Missense 6:149661836-149661836 - ccRCC-41 COSM1662563 c.2917C>A p.P973T Substitution - Missense 6:149662205-149662205 - TCGA-BQ-7048-01 COSM3994651 c.855C>A p.I285I Substitution - coding silent 6:149684234-149684234 - TCGA-AA-A00N-01 COSM275822 c.3170T>C p.V1057A Substitution - Missense 6:149661952-149661952 - CHC1053T COSM251014 c.2883+1G>T p.? Unknown 6:149676259-149676259 - RK050_C01 COSM1634559 c.2357C>A p.P786H Substitution - Missense 6:149680111-149680111 - 18 COSM5744901 c.143C>A p.A48D Substitution - Missense 6:149701984-149701984 - LUAD-CHTN-MAD06-00668 COSM360251 c.472C>T p.P158S Substitution - Missense 6:149695098-149695098 - TCGA-AX-A05Z-01 COSM1074449 c.2230C>T p.R744* Substitution - Nonsense 6:149680238-149680238 - TCGA-AX-A0J1-01 COSM1074467 c.134C>A p.S45Y Substitution - Missense 6:149701993-149701993 - TCGA-EK-A2H0-01 COSM4819046 c.1657C>G p.Q553E Substitution - Missense 6:149683432-149683432 - PD3945a COSM219259 c.3346C>G p.Q1116E Substitution - Missense 6:149661776-149661776 - TCGA-HU-A4H5-01 COSM3859000 c.3256G>T p.D1086Y Substitution - Missense 6:149661866-149661866 - TCGA-BS-A0UV-01 COSM1074445 c.2611G>T p.D871Y Substitution - Missense 6:149676720-149676720 - UM-SCC-17B COSM4598665 c.673C>G p.Q225E Substitution - Missense 6:149684416-149684416 - B74 COSM1754587 c.1517C>T p.P506L Substitution - Missense 6:149683572-149683572 - Gp2D COSM3018768 c.1950A>G p.V650V Substitution - coding silent 6:149683139-149683139 - STC252 COSM5061485 c.954A>G p.R318R Substitution - coding silent 6:149684135-149684135 - C135 COSM175052 c.2209C>T p.R737* Substitution - Nonsense 6:149680259-149680259 - HT115 COSM3018765 c.2065G>T p.E689* Substitution - Nonsense 6:149680403-149680403 - LUAD-RT-S01702 COSM392165 c.797delC p.P266fs*19 Deletion - Frameshift 6:149684292-149684292 - CHC1053T COSM251014 c.2883+1G>T p.? Unknown 6:149676259-149676259 - TCGA-BR-7851-01 COSM3859044 c.459A>T p.A153A Substitution - coding silent 6:149695111-149695111 - Gp5D COSM3018824 c.393A>G p.I131M Substitution - Missense 6:149695177-149695177 - T3024 COSM4697498 c.2008C>T p.R670W Substitution - Missense 6:149683081-149683081 - sysucc-1370T COSM3430102 c.1719C>T p.Y573Y Substitution - coding silent 6:149683370-149683370 - TCGA-BR-A4QL-01 COSM3859029 c.1334C>T p.P445L Substitution - Missense 6:149683755-149683755 - BN38 COSM3662196 c.2285A>T p.N762I Substitution - Missense 6:149680183-149680183 - TCGA-AC-A23H-01 COSM3829279 c.1029G>A p.G343G Substitution - coding silent 6:149684060-149684060 - TCGA-AZ-4315-01 COSM1441116 c.3282G>A p.P1094P Substitution - coding silent 6:149661840-149661840 - TCGA-C8-A26V-01 COSM1487312 c.108A>T p.E36D Substitution - Missense 6:149702019-149702019 - TCGA-AP-A0LD-01 COSM1074459 c.1155C>T p.S385S Substitution - coding silent 6:149683934-149683934 - ESCC_44 COSM5314048 c.3088A>G p.I1030V Substitution - Missense 6:149662034-149662034 - 8065650 COSM3393852 c.3164A>C p.E1055A Substitution - Missense 6:149661958-149661958 - CHC1053T COSM217373 c.2883+1C>A p.? Unknown TCGA-AA-3492-01 COSM1441140 c.179A>G p.E60G Substitution - Missense 6:149701948-149701948 - BN26 COSM1621050 c.2738C>T p.T913I Substitution - Missense 6:149676593-149676593 - T3080 COSM4697496 c.2241C>T p.V747V Substitution - coding silent 6:149680227-149680227 - ESO-2143 COSM1256339 c.245G>A p.R82Q Substitution - Missense 6:149701882-149701882 - Au1 COSM5596965 c.766C>T p.P256S Substitution - Missense 6:149684323-149684323 - LS411 COSM3018788 c.1419A>G p.A473A Substitution - coding silent 6:149683670-149683670 - TCGA-CL-5918-01 COSM1568018 c.2984G>A p.R995H Substitution - Missense 6:149662138-149662138 - TCGA-EK-A2RB-01 COSM4820020 c.2810G>T p.G937V Substitution - Missense 6:149676333-149676333 - PT17_1 COSM5898888 c.1597C>T p.P533S Substitution - Missense 6:149683492-149683492 - BN26T COSM1621050 c.2738C>T p.T913I Substitution - Missense 6:149676593-149676593 - BD134T COSM5494424 c.1315G>A p.A439T Substitution - Missense 6:149683774-149683774 - UM-SCC-17B COSM4598643 c.605C>T p.S202F Substitution - Missense 6:149684484-149684484 - SA106 COSM213788 c.962G>C p.S321T Substitution - Missense 6:149684127-149684127 - HCC121 COSM1621046 c.3030T>A p.F1010L Substitution - Missense 6:149662092-149662092 - NPC115D COSM4996616 c.1774G>A p.E592K Substitution - Missense 6:149683315-149683315 - EGC15 COSM5061483 c.3375C>T p.R1125R Substitution - coding silent 6:149661747-149661747 - TCGA-30-1891-01 COSM111362 c.233delT p.L78fs*54 Deletion - Frameshift 6:149701894-149701894 - 23 COSM4697498 c.2008C>T p.R670W Substitution - Missense 6:149683081-149683081 - TCGA-13-1483-01 COSM4946779 c.1517C>G p.P506R Substitution - Missense 6:149683572-149683572 - 3206A7_017_T COSM5038721 c.867_884del18 p.P290_A295delPVPPGA Deletion - In frame 6:149684205-149684222 - TCGA-Q1-A73O-01 COSM4835890 c.2045G>C p.R682T Substitution - Missense 6:149680423-149680423 - I2L-P10-Tumor-Organoid COSM5357118 c.3225C>A p.F1075L Substitution - Missense 6:149661897-149661897 - TCGA-CF-A3MG-01 COSM1311657 c.2587C>G p.Q863E Substitution - Missense 6:149679881-149679881 - RK307_C01 COSM3702905 c.2080C>T p.R694C Substitution - Missense 6:149680388-149680388 - B74-Tumor COSM1754587 c.1517C>T p.P506L Substitution - Missense 6:149683572-149683572 - 395 COSM4428715 c.1438C>T p.Q480* Substitution - Nonsense 6:149683651-149683651 - TCGA-R2-A69V-01 COSM4851095 c.2844T>G p.P948P Substitution - coding silent 6:149676299-149676299 - 12-P279 COSM4586306 c.3197A>G p.K1066R Substitution - Missense 6:149661925-149661925 - Pat_63_B COSM5869496 c.197G>A p.R66K Substitution - Missense 6:149701930-149701930 - TCGA-FP-A4BE-01 COSM3859038 c.504G>A p.V168V Substitution - coding silent 6:149684585-149684585 - ESCC_33 COSM5628335 c.3298G>A p.E1100K Substitution - Missense 6:149661824-149661824 - TCGA-BT-A3PJ-01 COSM3777183 c.103C>T p.R35W Substitution - Missense 6:149702024-149702024 - PT13 COSM5895841 c.2983C>T p.R995C Substitution - Missense 6:149662139-149662139 - 267T COSM1727232 c.1988A>T p.Q663L Substitution - Missense 6:149683101-149683101 - HCC159 COSM3662038 c.2648C>G p.S883* Substitution - Nonsense 6:149676683-149676683 - CSCC-11-T COSM4508924 c.791C>T p.P264L Substitution - Missense 6:149684298-149684298 - Gp2D COSM3018824 c.393A>G p.I131M Substitution - Missense 6:149695177-149695177 - TCGA-EE-A20C-06 COSM3621404 c.287G>A p.R96Q Substitution - Missense 6:149701840-149701840 - BK0034 COSM4187013 c.3105T>A p.D1035E Substitution - Missense 6:149662017-149662017 - sysucc-311T COSM5466706 c.2996A>C p.N999T Substitution - Missense 6:149662126-149662126 - S00050 COSM317555 c.599A>C p.Y200S Substitution - Missense 6:149684490-149684490 - YUAKER COSM1698122 c.923C>T p.S308F Substitution - Missense 6:149684166-149684166 - TCGA-CK-5916-01 COSM1441124 c.2064delA p.E689fs*18 Deletion - Frameshift 6:149680404-149680404 - TCGA-EK-A3GK-01 COSM4852985 c.3019C>T p.H1007Y Substitution - Missense 6:149662103-149662103 - AOCS-170-1-8 COSM4149168 c.2990G>T p.G997V Substitution - Missense 6:149662132-149662132 - LUAD-CHTN-3090416 COSM357650 c.2480G>C p.R827T Substitution - Missense 6:149679988-149679988 - TCGA-22-4613-01 COSM740637 c.73G>T p.V25F Substitution - Missense 6:149702054-149702054 - 8057680 COSM3393854 c.1750C>T p.Q584* Substitution - Nonsense 6:149683339-149683339 - 8064580 COSM4389019 c.1338C>G p.S446R Substitution - Missense 6:149683751-149683751 - CSCC-16-T COSM4561503 c.887G>A p.W296* Substitution - Nonsense 6:149684202-149684202 - HCC26T COSM3662040 c.269A>G p.N90S Substitution - Missense 6:149701858-149701858 - PT40 COSM5895841 c.2983C>T p.R995C Substitution - Missense 6:149662139-149662139 - YUMOKI COSM5404559 c.1391C>T p.S464F Substitution - Missense 6:149683698-149683698 - TCGA-EB-A3XC-01 COSM3621390 c.2942C>T p.A981V Substitution - Missense 6:149662180-149662180 - MCF7 COSM1672828 c.3127G>A p.D1043N Substitution - Missense 6:149661995-149661995 - AOCS-142-3-5 COSM4149170 c.2752G>T p.A918S Substitution - Missense 6:149676579-149676579 - TCGA-B5-A0JY-01 COSM1074463 c.298G>T p.E100* Substitution - Nonsense 6:149701829-149701829 - 4_RESISTANT COSM1724567 c.575_576insC p.P193fs*11 Insertion - Frameshift 6:149684513-149684514 - TCGA-F1-6177-01 COSM1256339 c.245G>A p.R82Q Substitution - Missense 6:149701882-149701882 - BD135T COSM5516379 c.3187G>T p.G1063* Substitution - Nonsense 6:149661935-149661935 - 397 COSM3018806 c.800C>T p.S267L Substitution - Missense 6:149684289-149684289 - DLD1 COSM4625689 c.2697A>G p.A899A Substitution - coding silent 6:149676634-149676634 - CSCC-31-T COSM4484729 c.2846C>T p.P949L Substitution - Missense 6:149676297-149676297 - BD165T COSM1441126 c.1986delA p.K662fs*3 Deletion - Frameshift 6:149683103-149683103 - 2521262 COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - LUAD-S01405 COSM399175 c.495A>G p.P165P Substitution - coding silent 6:149695075-149695075 - TCGA-66-2757-01 COSM740641 c.1518A>G p.P506P Substitution - coding silent 6:149683571-149683571 - TCGA-EX-A69M-01 COSM4829197 c.2770C>T p.R924* Substitution - Nonsense 6:149676561-149676561 - TCGA-BP-4807-01 COSM3366217 c.2355T>C p.I785I Substitution - coding silent 6:149680113-149680113 - TCGA-GF-A3OT-06 COSM3621401 c.804G>A p.W268* Substitution - Nonsense 6:149684285-149684285 - C135 COSM4611172 c.1498delA p.S500fs*5 Deletion - Frameshift 6:149683591-149683591 - YURIDA COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - 2492702 COSM5716365 c.3097C>T p.P1033S Substitution - Missense 6:149662025-149662025 - TCGA-CF-A1HR-01 COSM421038 c.1160C>T p.S387F Substitution - Missense 6:149683929-149683929 - RK050_C COSM1634559 c.2357C>A p.P786H Substitution - Missense 6:149680111-149680111 - HCT-15 COSM1672832 c.2552C>T p.T851I Substitution - Missense 6:149679916-149679916 - S00827 COSM312462 c.700G>C p.V234L Substitution - Missense 6:149684389-149684389 - BK0017 COSM4186016 c.3121C>T p.P1041S Substitution - Missense 6:149662001-149662001 - TCGA-AX-A0J0-01 COSM175052 c.2209C>T p.R737* Substitution - Nonsense 6:149680259-149680259 - PD7217a COSM5791859 c.2666A>G p.D889G Substitution - Missense 6:149676665-149676665 - TCGA-HU-A4G9-01 COSM3859048 c.232T>C p.L78L Substitution - coding silent 6:149701895-149701895 - 80 COSM5016166 c.2817_2818insT p.L940fs*3 Insertion - Frameshift 6:149676325-149676326 - HCC086T COSM5813126 c.1A>T p.M1L Substitution - Missense 6:149702126-149702126 - S00827 COSM312462 c.700G>C p.V234L Substitution - Missense 6:149684389-149684389 - CRC-04T COSM5468465 c.1554T>G p.S518S Substitution - coding silent 6:149683535-149683535 - Gp5D COSM3018768 c.1950A>G p.V650V Substitution - coding silent 6:149683139-149683139 - T2225 COSM4697494 c.2968C>T p.R990* Substitution - Nonsense 6:149662154-149662154 - ESCC_25 COSM5626936 c.253C>G p.L85V Substitution - Missense 6:149701874-149701874 - HCC26 COSM3662040 c.269A>G p.N90S Substitution - Missense 6:149701858-149701858 - YUQUEST COSM5404557 c.2711G>A p.R904Q Substitution - Missense 6:149676620-149676620 - RK052_C01 COSM1634561 c.2289A>G p.E763E Substitution - coding silent 6:149680179-149680179 - TCGA-29-1699-01 COSM1329274 c.2680T>A p.L894I Substitution - Missense 6:149676651-149676651 - TCGA-AZ-6598-01 COSM1441126 c.1986delA p.K662fs*3 Deletion - Frameshift 6:149683103-149683103 - TCGA-CI-6624-01 COSM1568016 c.830A>G p.Y277C Substitution - Missense 6:149684259-149684259 - HCC074T COSM5810176 c.4A>G p.K2E Substitution - Missense 6:149702123-149702123 - B109-Tumor COSM1754589 c.338G>A p.G113E Substitution - Missense 6:149701789-149701789 - AOCS-170-3-5 COSM4149168 c.2990G>T p.G997V Substitution - Missense 6:149662132-149662132 - TCGA-IR-A3LK-01 COSM4818260 c.751C>G p.P251A Substitution - Missense 6:149684338-149684338 - HCC4T COSM1621052 c.175A>G p.T59A Substitution - Missense 6:149701952-149701952 - TCGA-F5-6814-01 COSM3430102 c.1719C>T p.Y573Y Substitution - coding silent 6:149683370-149683370 - TCGA-AX-A0J0-01 COSM1074461 c.699A>C p.R233S Substitution - Missense 6:149684390-149684390 - TCGA-CG-5733-01 COSM3859020 c.1645G>T p.A549S Substitution - Missense 6:149683444-149683444 - TCGA-AA-3681-01 COSM268075 c.2369T>C p.M790T Substitution - Missense 6:149680099-149680099 - TCGA-BR-8680-01 COSM3859004 c.3045C>A p.F1015L Substitution - Missense 6:149662077-149662077 - TCGA-CG-5721-01 COSM3859032 c.1330T>C p.S444P Substitution - Missense 6:149683759-149683759 - sysucc-875T COSM1074465 c.244C>T p.R82* Substitution - Nonsense 6:149701883-149701883 - TCGA-A3-3349-01 COSM483524 c.1844T>C p.I615T Substitution - Missense 6:149683245-149683245 - T1154 COSM4697504 c.1074A>G p.I358M Substitution - Missense 6:149684015-149684015 - TCGA-AA-A02H-01 COSM287485 c.2969G>A p.R990Q Substitution - Missense 6:149662153-149662153 - 3N59-VS-3T59 COSM3018794 c.1196C>T p.S399L Substitution - Missense 6:149683893-149683893 - PT40 COSM5923727 c.2740C>T p.P914S Substitution - Missense 6:149676591-149676591 - T3021 COSM4697507 c.238G>T p.E80* Substitution - Nonsense 6:149701889-149701889 - S02294 COSM5688911 c.1879A>T p.R627W Substitution - Missense 6:149683210-149683210 - CRC-08T COSM4829197 c.2770C>T p.R924* Substitution - Nonsense 6:149676561-149676561 - ccRCC-10 COSM1662565 c.1785G>T p.K595N Substitution - Missense 6:149683304-149683304 - C467 COSM4442204 c.1094C>T p.A365V Substitution - Missense 6:149683995-149683995 - S00050 COSM317555 c.599A>C p.Y200S Substitution - Missense 6:149684490-149684490 - AOCS-063-1-3 COSM4149174 c.2275G>A p.E759K Substitution - Missense 6:149680193-149680193 - 464 COSM3702905 c.2080C>T p.R694C Substitution - Missense 6:149680388-149680388 - HCC127T COSM5822949 c.1404A>G p.P468P Substitution - coding silent 6:149683685-149683685 - CHC1053T COSM251014 c.2883+1G>T p.? Unknown 6:149676259-149676259 - LPJ108 COSM1316296 c.2850C>A p.F950L Substitution - Missense 6:149676293-149676293 - TCGA-AM-5821-01 COSM3697571 c.1669C>T p.P557S Substitution - Missense 6:149683420-149683420 - S02404 COSM5700882 c.2836G>T p.G946* Substitution - Nonsense 6:149676307-149676307 - BN38T COSM3662196 c.2285A>T p.N762I Substitution - Missense 6:149680183-149680183 - LAU165 COSM232668 c.787C>T p.P263S Substitution - Missense 6:149684302-149684302 - TCGA-22-4604-01 COSM740645 c.2561G>A p.R854K Substitution - Missense 6:149679907-149679907 - LIM2405 COSM4643054 c.3176A>G p.D1059G Substitution - Missense 6:149661946-149661946 - TCGA-GD-A3OP-01 COSM1311659 c.534G>A p.W178* Substitution - Nonsense 6:149684555-149684555 - TCGA-BS-A0UF-01 COSM275826 c.1923C>A p.F641L Substitution - Missense 6:149683166-149683166 - TCGA-BR-6452-01 COSM3859012 c.2034G>T p.Q678H Substitution - Missense 6:149680434-149680434 - PT08_1 COSM5893139 c.874C>T p.P292S Substitution - Missense 6:149684215-149684215 - 2290930 COSM4440058 c.3286C>T p.P1096S Substitution - Missense 6:149661836-149661836 - PT08_2 COSM5893139 c.874C>T p.P292S Substitution - Missense 6:149684215-149684215 - TCGA-F4-6570-01 COSM1441118 c.2645C>A p.P882H Substitution - Missense 6:149676686-149676686 - TCGA-CG-4443-01 COSM3859023 c.1509A>G p.V503V Substitution - coding silent 6:149683580-149683580 - TCGA-AP-A0LM-01 COSM1074455 c.1821G>T p.K607N Substitution - Missense 6:149683268-149683268 - TCGA-18-3409-01 COSM740647 c.2889C>T p.I963I Substitution - coding silent 6:149662233-149662233 - TCGA-39-5030-01 COSM740643 c.1923C>T p.F641F Substitution - coding silent 6:149683166-149683166 - TCGA-BR-6452-01 COSM3859008 c.2178T>C p.D726D Substitution - coding silent 6:149680290-149680290 - C086 COSM4697501 c.1592C>A p.P531H Substitution - Missense 6:149683497-149683497 - TCGA-EA-A6QX-01 COSM4828807 c.817C>T p.Q273* Substitution - Nonsense 6:149684272-149684272 - pfg019T COSM1642898 c.3373C>T p.R1125C Substitution - Missense 6:149661749-149661749 - 61 COSM1621052 c.175A>G p.T59A Substitution - Missense 6:149701952-149701952 - TCGA-DD-A3A0-01 COSM4934785 c.2759A>G p.E920G Substitution - Missense 6:149676572-149676572 - TCGA-AA-A00N-01 COSM275824 c.2231G>A p.R744Q Substitution - Missense 6:149680237-149680237 - RK133_C01 COSM1634563 c.1931A>G p.E644G Substitution - Missense 6:149683158-149683158 - AOCS-107-1-4 COSM4149172 c.2543G>T p.G848V Substitution - Missense 6:149679925-149679925 - CN-AML-NR-08-Dx COSM5425880 c.2484T>C p.D828D Substitution - coding silent 6:149679984-149679984 - TCGA-AA-A00N-01 COSM275826 c.1923C>A p.F641L Substitution - Missense 6:149683166-149683166 - 19M COSM5578869 c.860G>A p.R287Q Substitution - Missense 6:149684229-149684229 - NYU929 COSM4770784 c.378_379insT p.N127fs*1 Insertion - Frameshift 6:149695191-149695192 - TCGA-AN-A046-01 COSM3829275 c.2995A>G p.N999D Substitution - Missense 6:149662127-149662127 - T3091 COSM4697492 c.3030_3031insT p.K1011fs*1 Insertion - Frameshift 6:149662091-149662092 - ESCC_9 COSM5623678 c.2275G>T p.E759* Substitution - Nonsense 6:149680193-149680193 - TCGA-B9-5156-01 COSM3994649 c.2089A>G p.R697G Substitution - Missense 6:149680379-149680379 - TCGA-EE-A29D-06 COSM3621395 c.901C>T p.P301S Substitution - Missense 6:149684188-149684188 - TCGA-Q1-A5R2-01 COSM4850277 c.439C>T p.R147* Substitution - Nonsense 6:149695131-149695131 - TCGA-D1-A174-01 COSM1074453 c.1949T>C p.V650A Substitution - Missense 6:149683140-149683140 - TCGA-66-2783-01 COSM740649 c.2980G>A p.D994N Substitution - Missense 6:149662142-149662142 - PT40 COSM5923729 c.1573C>T p.Q525* Substitution - Nonsense 6:149683516-149683516 - CSCC-56-T COSM4453190 c.2634A>T p.E878D Substitution - Missense 6:149676697-149676697 - TCGA-EK-A2H0-01 COSM4819073 c.620C>G p.S207* Substitution - Nonsense 6:149684469-149684469 - HCC121T COSM1621046 c.3030T>A p.F1010L Substitution - Missense 6:149662092-149662092 - TCGA-BR-8680-01 COSM3859002 c.3112A>C p.N1038H Substitution - Missense 6:149662010-149662010 - Pat_26_A COSM5869494 c.2656C>T p.R886* Substitution - Nonsense 6:149676675-149676675 - HCT-116 COSM1684091 c.1593delT p.P533fs*8 Deletion - Frameshift 6:149683496-149683496 - CSCC-20-T COSM4453509 c.304A>T p.N102Y Substitution - Missense 6:149701823-149701823 - YUDAB COSM1698120 c.2346G>A p.M782I Substitution - Missense 6:149680122-149680122 - LC_S49 COSM1187176 c.1860C>A p.N620K Substitution - Missense 6:149683229-149683229 - PT13 COSM5895838 c.442C>T p.R148* Substitution - Nonsense 6:149695128-149695128 - T2269 COSM4697501 c.1592C>A p.P531H Substitution - Missense 6:149683497-149683497 - CSCC-17-T COSM4451969 c.1509A>T p.V503V Substitution - coding silent 6:149683580-149683580 - TCGA-DR-A0ZM-01 COSM461882 c.1604G>A p.G535E Substitution - Missense 6:149683485-149683485 - TCGA-CG-5721-01 COSM3859014 c.1842T>C p.P614P Substitution - coding silent 6:149683247-149683247 - CSCC-17-T COSM4539688 c.271G>A p.E91K Substitution - Missense 6:149701856-149701856 - TCGA-IR-A3LK-01 COSM4598665 c.673C>G p.Q225E Substitution - Missense 6:149684416-149684416 - T155 COSM175052 c.2209C>T p.R737* Substitution - Nonsense 6:149680259-149680259 - TCGA-AM-5821-01 COSM3761533 c.1446T>C p.S482S Substitution - coding silent 6:149683643-149683643 - TCGA-BR-4361-01 COSM3859017 c.1652A>G p.N551S Substitution - Missense 6:149683437-149683437 - TCGA-EE-A29L-06 COSM3621392 c.1703C>T p.P568L Substitution - Missense 6:149683386-149683386 - HX5T COSM1621048 c.2925T>C p.A975A Substitution - coding silent 6:149662197-149662197 - CN-AML-08-T COSM5425880 c.2484T>C p.D828D Substitution - coding silent 6:149679984-149679984 - I2L-P19Ta-Tumor-Organoid COSM5357280 c.2234A>G p.N745S Substitution - Missense 6:149680234-149680234 - TCGA-B0-5710-01 COSM483530 c.83G>A p.R28Q Substitution - Missense 6:149702044-149702044 - TCGA-D1-A161-01 COSM1074443 c.2695_2704del10 p.A899fs*5 Deletion - Frameshift 6:149676627-149676636 - TCGA-CD-A4MI-01 COSM3859041 c.482C>T p.A161V Substitution - Missense 6:149695088-149695088 - PT51 COSM5895841 c.2983C>T p.R995C Substitution - Missense 6:149662139-149662139 - 202_T COSM3948150 c.1250A>T p.H417L Substitution - Missense 6:149683839-149683839 - SS6003113 COSM3413919 c.1776G>C p.E592D Substitution - Missense 6:149683313-149683313 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.549077;Hs.549079;Hs.549084 6q25.1 603473

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.L78Cfs*54 c.233delT 6 150023030 OV A G Missense p.M790T c.2369T>C 6 150001235 COREAD A G Synonymous p.I785I c.2355T>C 6 150001249 RCCC A - IntronicDeletion . c.349-20delT 6 150016377 STAD C A Missense p.A549S c.1645G>T 6 150004580 STAD C A Missense p.R252I c.755G>T 6 150005470 LUAD C A Missense p.R744L c.2231G>T 6 150001373 LUAD C A Missense p.R767L c.2300G>T 6 150001304 HNSC C A Missense p.V25F c.73G>T 6 150023190 LUSC C A Synonymous p.P192P c.576G>T 6 150005649 LUSC C A Synonymous p.S1111S c.3333G>T 6 149982925 LUAD C A Synonymous p.S1111S c.3333G>T 6 149982925 STAD CCCT - Frameshift p.G392Dfs*17 c.1173_1176delAGGG 6 150005049 CLL C G Missense p.D837H c.2509G>C 6 150001095 HNSC C G Missense p.M643I c.1929G>C 6 150004296 CM C G Missense p.R1020T c.3059G>C 6 149983199 OV C G Missense p.S321T c.962G>C 6 150005263 BRCA C G Missense p.S803T c.2408G>C 6 150001196 LUAD C G Missense p.V234L c.700G>C 6 150005525 SCLC C G Synonymous p.S1111S c.3333G>C 6 149982925 CM C T Missense p.A748T c.2242G>A 6 150001362 OV C T Missense p.D994N c.2980G>A 6 149983278 LUSC C T Missense p.G554E c.1661G>A 6 150004564 RCCC C T Missense p.M419I c.1257G>A 6 150004968 LUAD C T Missense p.R1082K c.3245G>A 6 149983013 STAD C T Missense p.R28Q c.83G>A 6 150023180 RCCC C T Missense p.R82Q c.245G>A 6 150023018 ESCA C T Missense p.R82Q c.245G>A 6 150023018 STAD C T Missense p.R854K c.2561G>A 6 150001043 LUSC C T Missense p.R96Q c.287G>A 6 150022976 CM C T Missense p.R990Q c.2969G>A 6 149983289 COREAD C T Nonsense p.W178* c.534G>A 6 150005691 BLCA C T SpliceAcceptorSNV . c.497-1G>A 6 150005729 HNSC G A Missense p.H475Y c.1423C>T 6 150004802 CM G A Missense p.P375S c.1123C>T 6 150005102 HNSC G A Missense p.P468S c.1402C>T 6 150004823 CM G A Missense p.P568L c.1703C>T 6 150004522 CM G A Missense p.P579S c.1735C>T 6 150004490 UCEC G A Missense p.R1125C c.3373C>T 6 149982885 STAD G A Missense p.R35W c.103C>T 6 150023160 BLCA G A Missense p.R502C c.1504C>T 6 150004721 LUAD G A Missense p.R502C c.1504C>T 6 150004721 STAD G A Missense p.R657C c.1969C>T 6 150004256 UCEC G A Missense p.R694C c.2080C>T 6 150001524 OV G A Missense p.S387F c.1160C>T 6 150005065 BLCA G A Missense p.S438F c.1313C>T 6 150004912 CM G A Missense p.S84F c.251C>T 6 150023012 MM G A Missense p.V719I c.2155G>A 6 150001449 GBM G A Nonsense p.R737* c.2209C>T 6 150001395 BRCA G A Synonymous p.F641F c.1923C>T 6 150004302 LUSC G A Synonymous p.S385S c.1155C>T 6 150005070 UCEC G C Missense p.I288M c.864C>G 6 150005361 BLCA G C Missense p.P1028A c.3082C>G 6 149983176 BRCA G C Missense p.P506R c.1517C>G 6 150004708 OV G C Missense p.Q863E c.2587C>G 6 150001017 BLCA G C Missense p.S1023C c.3068C>G 6 149983190 HNSC GCTGGCGTGC - Frameshift p.A899Tfs*5 c.2695_2704delGCACGCCAGC 6 149997763 UCEC GG AA Missense p.R287* c.858_859delinsTT 6 150005366 CM GG TA IntronicBlockSubstitution . c.349-1938_349-1937delinsTA 6 150018294 CM G T Missense p.P1028T c.3082C>A 6 149983176 OV G T Missense p.P786H c.2357C>A 6 150001247 HC G T Missense p.T255N c.764C>A 6 150005461 LUAD TAGCAACACTT - Frameshift p.E920Afs*9 c.2759_2769delAAGTGTTGCTA 6 149997698 BRCA T A Missense p.E36D c.108A>T 6 150023155 BRCA T A Synonymous p.T954T c.2862A>T 6 149997417 HNSC T C Missense p.E644G c.1931A>G 6 150004294 HC T C Missense p.H820R c.2459A>G 6 150001145 LUAD T C Missense p.N471S c.1412A>G 6 150004813 LUAD T C Missense p.N762S c.2285A>G 6 150001319 LUAD T C Synonymous p.K662K c.1986A>G 6 150004239 OV T C Synonymous p.P506P c.1518A>G 6 150004707 LUSC T C Synonymous p.V503V c.1509A>G 6 150004716 STAD T - Frameshift p.F88Lfs*44 c.261delA 6 150023002 THCA T G Missense p.Y200S c.599A>C 6 150005626 SCLC T - IntronicDeletion . c.2884-136delA 6 149983510 ESCA