Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 3 52437564 52437565 + Frame_Shift_Ins INS - - A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr3:52437564_52437565insA c.1596_1597insT c.(1594-1599)tttggafs p.G533fs ACC 3 52438537 52438537 + Silent SNP G G A TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr3:52438537G>A c.1182C>T c.(1180-1182)taC>taT p.Y394Y BLCA 3 52436687 52436687 + Missense_Mutation SNP C C G TCGA-HQ-A2OE-01A-11D-A202-08 TCGA-HQ-A2OE-10A-01D-A202-08 g.chr3:52436687C>G c.1987G>C c.(1987-1989)Gat>Cat p.D663H BLCA 3 52436687 52436687 + Missense_Mutation SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr3:52436687C>T c.1987G>A c.(1987-1989)Gat>Aat p.D663N BLCA 3 52436810 52436810 + Missense_Mutation SNP C C G TCGA-HQ-A2OE-01A-11D-A202-08 TCGA-HQ-A2OE-10A-01D-A202-08 g.chr3:52436810C>G c.1968G>C c.(1966-1968)aaG>aaC p.K656N BLCA 3 52436887 52436887 + Splice_Site SNP C C A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr3:52436887C>A c.1891G>T c.(1891-1893)Gag>Tag p.E631* BLCA 3 52436887 52436887 + Splice_Site SNP C C G TCGA-FJ-A3Z7-01A-12D-A23M-08 TCGA-FJ-A3Z7-10A-01D-A23K-08 g.chr3:52436887C>G c.1891G>C c.(1891-1893)Gag>Cag p.E631Q BLCA 3 52437315 52437315 + Splice_Site SNP C C G TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr3:52437315C>G c.e14-1 BLCA 3 52437490 52437490 + Missense_Mutation SNP G G C TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr3:52437490G>C c.1671C>G c.(1669-1671)atC>atG p.I557M BLCA 3 52437805 52437805 + Silent SNP G G C TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr3:52437805G>C c.1356C>G c.(1354-1356)ctC>ctG p.L452L BLCA 3 52437911 52437911 + Splice_Site SNP C C G TCGA-4Z-AA89-01A-11D-A391-08 TCGA-4Z-AA89-10A-01D-A394-08 g.chr3:52437911C>G c.e13-1 BLCA 3 52439230 52439230 + Missense_Mutation SNP G G A TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr3:52439230G>A c.1012C>T c.(1012-1014)Cct>Tct p.P338S BLCA 3 52439898 52439898 + Nonsense_Mutation SNP G G A TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr3:52439898G>A c.814C>T c.(814-816)Cag>Tag p.Q272* BLCA 3 52440365 52440370 + In_Frame_Del DEL GTTGAA GTTGAA - TCGA-XF-A8HI-01A-11D-A38G-08 TCGA-XF-A8HI-10A-01D-A38J-08 g.chr3:52440365_52440370delGTTGAA c.682_687delTTCAAC c.(682-687)ttcaacdel p.FN228del BLCA 3 52440379 52440379 + Missense_Mutation SNP C C G TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr3:52440379C>G c.673G>C c.(673-675)Gac>Cac p.D225H BLCA 3 52441219 52441219 + Missense_Mutation SNP T T G TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr3:52441219T>G c.551A>C c.(550-552)gAt>gCt p.D184A BLCA 3 52441220 52441220 + Missense_Mutation SNP C C T TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr3:52441220C>T c.550G>A c.(550-552)Gat>Aat p.D184N BLCA 3 52441221 52441221 + Silent SNP C C T TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr3:52441221C>T c.549G>A c.(547-549)ctG>ctA p.L183L BLCA 3 52441226 52441226 + Missense_Mutation SNP C C T TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr3:52441226C>T c.544G>A c.(544-546)Gag>Aag p.E182K BLCA 3 52441328 52441328 + Missense_Mutation SNP C C T TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr3:52441328C>T c.442G>A c.(442-444)Gag>Aag p.E148K BLCA 3 52441434 52441434 + Missense_Mutation SNP C C T TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr3:52441434C>T c.418G>A c.(418-420)Gcc>Acc p.A140T BLCA 3 52442080 52442080 + 5'Flank SNP G G C TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr3:52442080G>C BLCA 3 52442604 52442604 + 5'Flank SNP G G C TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr3:52442604G>C BLCA 3 52443754 52443754 + 5'Flank SNP A A C TCGA-DK-A6AV-01A-12D-A30E-08 TCGA-DK-A6AV-10A-01D-A30H-08 g.chr3:52443754A>C BRCA 3 52437465 52437465 + Missense_Mutation SNP C C T TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr3:52437465C>T c.1696G>A c.(1696-1698)Gag>Aag p.E566K BRCA 3 52437870 52437870 + Missense_Mutation SNP C C T TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr3:52437870C>T c.1291G>A c.(1291-1293)Ggt>Agt p.G431S BRCA 3 52440862 52440862 + Missense_Mutation SNP G G C TCGA-HN-A2OB-01A-21D-A27P-09 TCGA-HN-A2OB-10B-01D-A27P-09 g.chr3:52440862G>C c.642C>G c.(640-642)atC>atG p.I214M BRCA 3 52440864 52440865 + Frame_Shift_Ins INS - - A TCGA-AC-A62X-01A-11D-A29N-09 TCGA-AC-A62X-10A-01D-A29N-09 g.chr3:52440864_52440865insA c.639_640insT c.(637-642)cgtatcfs p.I214fs BRCA 3 52442072 52442072 + 5'Flank SNP T T C TCGA-E2-A573-01A-11D-A29N-09 TCGA-E2-A573-10A-01D-A29N-09 g.chr3:52442072T>C BRCA 3 52442600 52442600 + 5'Flank SNP G G C TCGA-A2-A0EQ-01A-11W-A050-09 TCGA-A2-A0EQ-10A-01W-A055-09 g.chr3:52442600G>C BRCA 3 52442611 52442611 + 5'Flank SNP C C T TCGA-A2-A0YE-01A-11D-A10G-09 TCGA-A2-A0YE-10A-01D-A10G-09 g.chr3:52442611C>T CESC 3 52437782 52437782 + Nonsense_Mutation SNP G G C TCGA-C5-A1BM-01A-11D-A13W-08 TCGA-C5-A1BM-10A-01D-A13W-08 g.chr3:52437782G>C c.1379C>G c.(1378-1380)tCa>tGa p.S460* CESC 3 52437848 52437848 + Nonsense_Mutation SNP G G C TCGA-EK-A2RC-01A-11D-A18J-09 TCGA-EK-A2RC-10A-01D-A18J-09 g.chr3:52437848G>C c.1313C>G c.(1312-1314)tCa>tGa p.S438* CESC 3 52439883 52439883 + Nonsense_Mutation SNP G G A TCGA-EA-A44S-01A-12D-A26G-09 TCGA-EA-A44S-10A-01D-A26G-09 g.chr3:52439883G>A c.829C>T c.(829-831)Caa>Taa p.Q277* CESC 3 52439883 52439883 + Nonsense_Mutation SNP G G A TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chr3:52439883G>A c.829C>T c.(829-831)Caa>Taa p.Q277* CHOL 3 52436651 52436667 + Frame_Shift_Del DEL TGAACTCATCGTAGTTG TGAACTCATCGTAGTTG - TCGA-3X-AAVE-01A-11D-A417-09 TCGA-3X-AAVE-10A-01D-A41A-09 g.chr3:52436651_52436667delTGAACTCATCGTAGTTG c.2007_2023delCAACTACGATGAGTTCA c.(2005-2025)cacaactacgatgagttcatcfs p.NYDEFI670fs CHOL 3 52437221 52437221 + Frame_Shift_Del DEL T T - TCGA-ZH-A8Y4-01A-11D-A417-09 TCGA-ZH-A8Y4-10A-01D-A41A-09 g.chr3:52437221delT c.1823delA c.(1822-1824)gacfs p.D608fs CHOL 3 52437802 52437802 + Frame_Shift_Del DEL T T - TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr3:52437802delT c.1359delA c.(1357-1359)aaafs p.K453fs CHOL 3 52437805 52437805 + Silent SNP G G A TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr3:52437805G>A c.1356C>T c.(1354-1356)ctC>ctT p.L452L CHOL 3 52439916 52439916 + Missense_Mutation SNP T T G TCGA-4G-AAZT-01A-11D-A417-09 TCGA-4G-AAZT-10A-01D-A41A-09 g.chr3:52439916T>G c.796A>C c.(796-798)Aca>Cca p.T266P CHOL 3 52439930 52439930 + Splice_Site SNP T T C TCGA-4G-AAZT-01A-11D-A417-09 TCGA-4G-AAZT-10A-01D-A41A-09 g.chr3:52439930T>C c.e10-2 CHOL 3 52440307 52440307 + Nonsense_Mutation SNP T T A TCGA-W5-AA2W-01A-11D-A417-09 TCGA-W5-AA2W-10A-01D-A41A-09 g.chr3:52440307T>A c.745A>T c.(745-747)Aag>Tag p.K249* CHOL 3 52440916 52440916 + Nonsense_Mutation SNP C C T TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr3:52440916C>T c.588G>A c.(586-588)tgG>tgA p.W196* CHOL 3 52441997 52441997 + 5'Flank SNP A A C TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr3:52441997A>C CHOL 3 52442599 52442599 + 5'Flank SNP A A G TCGA-ZH-A8Y2-01A-11D-A417-09 TCGA-ZH-A8Y2-10A-01D-A41A-09 g.chr3:52442599A>G COAD 3 52436306 52436306 + Nonstop_Mutation SNP A A G TCGA-F4-6807-01A-11D-1835-10 TCGA-F4-6807-10A-01D-1835-10 g.chr3:52436306A>G c.2188T>C c.(2188-2190)Tga>Cga p.*730R COAD 3 52436342 52436342 + Missense_Mutation SNP G G A TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr3:52436342G>A c.2152C>T c.(2152-2154)Cgg>Tgg p.R718W COAD 3 52436619 52436619 + Splice_Site SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr3:52436619T>C c.2055A>G c.(2053-2055)gaA>gaG p.E685E COAD 3 52436804 52436804 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr3:52436804C>T c.1974G>A c.(1972-1974)aaG>aaA p.K658K COAD 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R COAD 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R COAD 3 52437235 52437235 + Silent SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:52437235G>A c.1809C>T c.(1807-1809)gtC>gtT p.V603V COAD 3 52437627 52437627 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr3:52437627G>A c.1534C>T c.(1534-1536)Cgc>Tgc p.R512C COAD 3 52437823 52437823 + Silent SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr3:52437823G>A c.1338C>T c.(1336-1338)aaC>aaT p.N446N COAD 3 52438537 52438537 + Silent SNP G G A TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr3:52438537G>A c.1182C>T c.(1180-1182)taC>taT p.Y394Y COAD 3 52438566 52438566 + Nonsense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr3:52438566G>A c.1153C>T c.(1153-1155)Cga>Tga p.R385* COAD 3 52439816 52439816 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:52439816T>C c.896A>G c.(895-897)aAc>aGc p.N299S COAD 3 52439898 52439898 + Nonsense_Mutation SNP G G A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr3:52439898G>A c.814C>T c.(814-816)Cag>Tag p.Q272* COAD 3 52439930 52439930 + Splice_Site SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr3:52439930T>A c.e10-2 COAD 3 52439930 52439930 + Splice_Site SNP T T A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr3:52439930T>A c.e10-2 COAD 3 52440295 52440295 + Missense_Mutation SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:52440295G>T c.757C>A c.(757-759)Cag>Aag p.Q253K COAD 3 52440885 52440885 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr3:52440885G>A c.619C>T c.(619-621)Cgg>Tgg p.R207W COAD 3 52440917 52440917 + Nonsense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:52440917C>T c.587G>A c.(586-588)tGg>tAg p.W196* COAD 3 52441212 52441212 + Silent SNP C C T TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr3:52441212C>T c.558G>A c.(556-558)ctG>ctA p.L186L COAD 3 52442076 52442076 + 5'Flank SNP A A G TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:52442076A>G COAD 3 52442076 52442076 + 5'Flank SNP A A G TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr3:52442076A>G COAD 3 52442078 52442078 + 5'Flank SNP A A G TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr3:52442078A>G COAD 3 52442503 52442503 + 5'Flank SNP A A G TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr3:52442503A>G COAD 3 52442504 52442504 + 5'Flank SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:52442504A>G COAD 3 52442558 52442558 + 5'Flank SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr3:52442558A>G COAD 3 52442558 52442558 + 5'Flank SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr3:52442558A>G COAD 3 52443572 52443572 + 5'Flank SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr3:52443572C>T COAD 3 52443586 52443586 + 5'Flank SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr3:52443586G>A COADREAD 3 52436306 52436306 + Nonstop_Mutation SNP A A G TCGA-F4-6807-01A-11D-1835-10 TCGA-F4-6807-10A-01D-1835-10 g.chr3:52436306A>G c.2188T>C c.(2188-2190)Tga>Cga p.*730R COADREAD 3 52436342 52436342 + Missense_Mutation SNP G G A TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr3:52436342G>A c.2152C>T c.(2152-2154)Cgg>Tgg p.R718W COADREAD 3 52436345 52436345 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:52436345G>A c.2149C>T c.(2149-2151)Cgg>Tgg p.R717W COADREAD 3 52436619 52436619 + Splice_Site SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr3:52436619T>C c.2055A>G c.(2053-2055)gaA>gaG p.E685E COADREAD 3 52436804 52436804 + Silent SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr3:52436804C>T c.1974G>A c.(1972-1974)aaG>aaA p.K658K COADREAD 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R COADREAD 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R COADREAD 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R COADREAD 3 52437235 52437235 + Silent SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:52437235G>A c.1809C>T c.(1807-1809)gtC>gtT p.V603V COADREAD 3 52437627 52437627 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr3:52437627G>A c.1534C>T c.(1534-1536)Cgc>Tgc p.R512C COADREAD 3 52437823 52437823 + Silent SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr3:52437823G>A c.1338C>T c.(1336-1338)aaC>aaT p.N446N COADREAD 3 52438537 52438537 + Silent SNP G G A TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr3:52438537G>A c.1182C>T c.(1180-1182)taC>taT p.Y394Y COADREAD 3 52438566 52438566 + Nonsense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr3:52438566G>A c.1153C>T c.(1153-1155)Cga>Tga p.R385* COADREAD 3 52439816 52439816 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr3:52439816T>C c.896A>G c.(895-897)aAc>aGc p.N299S COADREAD 3 52439898 52439898 + Nonsense_Mutation SNP G G A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr3:52439898G>A c.814C>T c.(814-816)Cag>Tag p.Q272* COADREAD 3 52439930 52439930 + Splice_Site SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr3:52439930T>A c.e10-2 COADREAD 3 52439930 52439930 + Splice_Site SNP T T A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr3:52439930T>A c.e10-2 COADREAD 3 52440295 52440295 + Missense_Mutation SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr3:52440295G>T c.757C>A c.(757-759)Cag>Aag p.Q253K COADREAD 3 52440885 52440885 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr3:52440885G>A c.619C>T c.(619-621)Cgg>Tgg p.R207W COADREAD 3 52440917 52440917 + Nonsense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:52440917C>T c.587G>A c.(586-588)tGg>tAg p.W196* COADREAD 3 52441212 52441212 + Silent SNP C C T TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr3:52441212C>T c.558G>A c.(556-558)ctG>ctA p.L186L COADREAD 3 52442076 52442076 + 5'Flank SNP A A G TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr3:52442076A>G COADREAD 3 52442076 52442076 + 5'Flank SNP A A G TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr3:52442076A>G COADREAD 3 52442078 52442078 + 5'Flank SNP A A G TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr3:52442078A>G COADREAD 3 52442503 52442503 + 5'Flank SNP A A G TCGA-G4-6626-01A-11D-1771-10 TCGA-G4-6626-10A-01D-1771-10 g.chr3:52442503A>G COADREAD 3 52442504 52442504 + 5'Flank SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:52442504A>G COADREAD 3 52442558 52442558 + 5'Flank SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr3:52442558A>G COADREAD 3 52442558 52442558 + 5'Flank SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr3:52442558A>G COADREAD 3 52443572 52443572 + 5'Flank SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr3:52443572C>T COADREAD 3 52443586 52443586 + 5'Flank SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr3:52443586G>A ESCA 3 52439267 52439267 + Silent SNP G G A TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr3:52439267G>A c.975C>T c.(973-975)tcC>tcT p.S325S GBM 3 52442518 52442518 + 5'Flank SNP A A G TCGA-26-5133-01A-01D-1486-08 TCGA-26-5133-10A-01D-1486-08 g.chr3:52442518A>G GBMLGG 3 52442518 52442518 + 5'Flank SNP A A G TCGA-26-5133-01A-01D-1486-08 TCGA-26-5133-10A-01D-1486-08 g.chr3:52442518A>G HNSC 3 52437163 52437163 + Silent SNP G G A TCGA-F7-A61S-01A-11D-A28R-08 TCGA-F7-A61S-10A-01D-A28U-08 g.chr3:52437163G>A c.1881C>T c.(1879-1881)taC>taT p.Y627Y HNSC 3 52437288 52437288 + Missense_Mutation SNP T T G TCGA-CN-5364-01A-01D-1434-08 TCGA-CN-5364-10A-01D-1434-08 g.chr3:52437288T>G c.1756A>C c.(1756-1758)Atc>Ctc p.I586L HNSC 3 52439912 52439913 + Frame_Shift_Del DEL TG TG - TCGA-CV-7263-01A-11D-2012-08 TCGA-CV-7263-10A-01D-2013-08 g.chr3:52439912_52439913delTG c.799_800delCA c.(799-801)cagfs p.Q267fs HNSC 3 52441440 52441440 + Missense_Mutation SNP C C T TCGA-BA-5556-01A-01D-1512-08 TCGA-BA-5556-10A-01D-1512-08 g.chr3:52441440C>T c.412G>A c.(412-414)Gcc>Acc p.A138T KIPAN 3 52436345 52436345 + Frame_Shift_Del DEL G G - TCGA-B8-4151-01A-01D-1806-10 TCGA-B8-4151-10A-01D-1251-10 g.chr3:52436345delG c.2149delC c.(2149-2151)cggfs p.R718fs KIPAN 3 52436362 52436362 + Frame_Shift_Del DEL T T - TCGA-B0-5699-01A-11D-1534-10 TCGA-B0-5699-11A-01D-1534-10 g.chr3:52436362delT c.2132delA c.(2131-2133)aagfs p.K711fs KIPAN 3 52436397 52436397 + Frame_Shift_Del DEL C C - TCGA-BP-5174-01A-01D-1429-08 TCGA-BP-5174-11A-01D-1429-08 g.chr3:52436397delC c.2097delG c.(2095-2097)cggfs p.R701fs KIPAN 3 52436403 52436403 + Frame_Shift_Del DEL G G - TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr3:52436403delG c.2091delC c.(2089-2091)tccfs p.S697fs KIPAN 3 52437163 52437163 + Nonsense_Mutation SNP G G C TCGA-B8-4143-01A-01D-1806-10 TCGA-B8-4143-11A-01D-1251-10 g.chr3:52437163G>C c.1881C>G c.(1879-1881)taC>taG p.Y627* KIPAN 3 52437168 52437168 + Nonsense_Mutation SNP T T A TCGA-CJ-4923-01A-01D-1429-08 TCGA-CJ-4923-11A-01D-1429-08 g.chr3:52437168T>A c.1876A>T c.(1876-1878)Aaa>Taa p.K626* KIPAN 3 52437530 52437533 + Frame_Shift_Del DEL ATGC ATGC - TCGA-CW-6097-01A-11D-1669-08 TCGA-CW-6097-11A-01D-1669-08 g.chr3:52437530_52437533delATGC c.1628_1631delGCAT c.(1627-1632)tgcatafs p.CI543fs KIPAN 3 52437652 52437652 + Frame_Shift_Del DEL G G - TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr3:52437652delG c.1509delC c.(1507-1509)ttcfs p.F503fs KIPAN 3 52437657 52437657 + Missense_Mutation SNP C C G TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr3:52437657C>G c.1504G>C c.(1504-1506)Gct>Cct p.A502P KIPAN 3 52437709 52437709 + Frame_Shift_Del DEL G G - TCGA-G7-A8LD-01A-11D-A35Z-10 TCGA-G7-A8LD-10A-01D-A35Z-10 g.chr3:52437709delG c.1452delC c.(1450-1452)cccfs p.P484fs KIPAN 3 52437782 52437782 + Nonsense_Mutation SNP G G C TCGA-B0-5095-01A-01D-1421-08 TCGA-B0-5095-11A-01D-1421-08 g.chr3:52437782G>C c.1379C>G c.(1378-1380)tCa>tGa p.S460* KIPAN 3 52437846 52437846 + Missense_Mutation SNP C C A TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr3:52437846C>A c.1315G>T c.(1315-1317)Gtg>Ttg p.V439L KIPAN 3 52437889 52437889 + Frame_Shift_Del DEL C C - TCGA-AL-3473-01A-01D-1252-08 TCGA-AL-3473-10A-01D-1252-08 g.chr3:52437889delC c.1272delG c.(1270-1272)gggfs p.G424fs KIPAN 3 52438499 52438499 + Frame_Shift_Del DEL T T - TCGA-CZ-5452-01A-01D-1501-10 TCGA-CZ-5452-11A-01D-1501-10 g.chr3:52438499delT c.1220delA c.(1219-1221)gatfs p.D408fs KIPAN 3 52438515 52438515 + Nonsense_Mutation SNP C C A TCGA-A3-3317-01A-01D-0966-08 TCGA-A3-3317-11A-01D-0966-08 g.chr3:52438515C>A c.1204G>T c.(1204-1206)Gag>Tag p.E402* KIPAN 3 52439133 52439133 + Missense_Mutation SNP G G T TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr3:52439133G>T c.1109C>A c.(1108-1110)cCc>cAc p.P370H KIPAN 3 52439196 52439196 + Frame_Shift_Del DEL T T - TCGA-CJ-4869-01A-02D-1429-08 TCGA-CJ-4869-11A-01D-1429-08 g.chr3:52439196delT c.1046delA c.(1045-1047)aacfs p.N349fs KIPAN 3 52439219 52439238 + Frame_Shift_Del DEL GCTGCCTGGAGGCTTCACCA GCTGCCTGGAGGCTTCACCA - TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr3:52439219_52439238delGCTGCCTGGAGGCTTCACCA c.1004_1023delTGGTGAAGCCTCCAGGCAGC c.(1003-1023)gtggtgaagcctccaggcagcfs p.VVKPPGS335fs KIPAN 3 52439271 52439271 + Frame_Shift_Del DEL G G - TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr3:52439271delG c.971delC c.(970-972)ccafs p.P324fs KIPAN 3 52439275 52439275 + Missense_Mutation SNP C C A TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr3:52439275C>A c.967G>T c.(967-969)Gcc>Tcc p.A323S KIPAN 3 52439306 52439306 + Silent SNP A A C TCGA-B0-4842-01A-02D-1421-08 TCGA-B0-4842-11A-01D-1421-08 g.chr3:52439306A>C c.936T>G c.(934-936)ggT>ggG p.G312G KIPAN 3 52439311 52439311 + Splice_Site SNP C C A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr3:52439311C>A c.e11-1 KIPAN 3 52439781 52439781 + Splice_Site SNP C C A TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr3:52439781C>A c.931G>T c.(931-933)Gat>Tat p.D311Y KIPAN 3 52439864 52439864 + Frame_Shift_Del DEL T T - TCGA-B0-4827-01A-02D-1421-08 TCGA-B0-4827-11A-01D-1421-08 g.chr3:52439864delT c.848delA c.(847-849)gagfs p.E284fs KIPAN 3 52439876 52439876 + Nonsense_Mutation SNP G G T TCGA-BP-4163-01A-02D-1386-10 TCGA-BP-4163-11A-01D-1251-10 g.chr3:52439876G>T c.836C>A c.(835-837)tCa>tAa p.S279* KIPAN 3 52439900 52439900 + Missense_Mutation SNP A A G TCGA-BQ-5877-01A-11D-1589-08 TCGA-BQ-5877-11A-01D-1589-08 g.chr3:52439900A>G c.812T>C c.(811-813)aTt>aCt p.I271T KIPAN 3 52439913 52439913 + Nonsense_Mutation SNP G G A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr3:52439913G>A c.799C>T c.(799-801)Cag>Tag p.Q267* KIPAN 3 52440295 52440295 + Nonsense_Mutation SNP G G A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr3:52440295G>A c.757C>T c.(757-759)Cag>Tag p.Q253* KIPAN 3 52440367 52440367 + Missense_Mutation SNP T T G TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr3:52440367T>G c.685A>C c.(685-687)Aac>Cac p.N229H KIPAN 3 52441190 52441190 + Splice_Site SNP C C T TCGA-BQ-5875-01A-11D-1589-08 TCGA-BQ-5875-11A-01D-1589-08 g.chr3:52441190C>T c.580G>A c.(580-582)Ggg>Agg p.G194R KIPAN 3 52441229 52441230 + Frame_Shift_Del DEL AG AG - TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr3:52441229_52441230delAG c.540_541delCT c.(538-543)ctctttfs p.F181fs KIPAN 3 52441261 52441261 + Missense_Mutation SNP A A C TCGA-CZ-5469-01A-01D-1501-10 TCGA-CZ-5469-11A-01D-1501-10 g.chr3:52441261A>C c.509T>G c.(508-510)tTt>tGt p.F170C KIPAN 3 52441262 52441262 + Missense_Mutation SNP A A C TCGA-B0-5097-01A-01D-1421-08 TCGA-B0-5097-11A-01D-1421-08 g.chr3:52441262A>C c.508T>G c.(508-510)Ttt>Gtt p.F170V KIPAN 3 52441304 52441304 + Nonsense_Mutation SNP G G A TCGA-CJ-4641-01A-02D-1386-10 TCGA-CJ-4641-11A-01D-1251-10 g.chr3:52441304G>A c.466C>T c.(466-468)Cag>Tag p.Q156* KIPAN 3 52441417 52441417 + Silent SNP G G C TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr3:52441417G>C c.435C>G c.(433-435)gcC>gcG p.A145A KIPAN 3 52441418 52441418 + Missense_Mutation SNP G G C TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr3:52441418G>C c.434C>G c.(433-435)gCc>gGc p.A145G KIPAN 3 52441470 52441470 + Nonsense_Mutation SNP C C A TCGA-B0-4691-01A-01D-1361-10 TCGA-B0-4691-11A-01D-1361-10 g.chr3:52441470C>A c.382G>T c.(382-384)Gga>Tga p.G128* KIPAN 3 52442023 52442023 + 5'Flank SNP C C A TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr3:52442023C>A KIPAN 3 52442512 52442512 + 5'Flank SNP T T C TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr3:52442512T>C KIPAN 3 52442512 52442512 + 5'Flank SNP T T C TCGA-CJ-4637-01A-02D-1386-10 TCGA-CJ-4637-11A-01D-1251-10 g.chr3:52442512T>C KIPAN 3 52442521 52442521 + 5'Flank SNP T T C TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr3:52442521T>C KIPAN 3 52442523 52442523 + 5'Flank DEL A A - TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr3:52442523delA KIPAN 3 52442567 52442567 + 5'Flank SNP G G A TCGA-BP-4337-01A-01D-1366-10 TCGA-BP-4337-11A-01D-1366-10 g.chr3:52442567G>A KIPAN 3 52442600 52442600 + 5'Flank SNP G G C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr3:52442600G>C KIPAN 3 52443568 52443568 + 5'Flank SNP A A G TCGA-CJ-4636-01A-02D-1386-10 TCGA-CJ-4636-11A-01D-1251-10 g.chr3:52443568A>G KIPAN 3 52443568 52443568 + 5'Flank SNP A A T TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr3:52443568A>T KIPAN 3 52443574 52443574 + 5'Flank SNP G G A TCGA-CJ-4638-01A-02D-1386-10 TCGA-CJ-4638-11A-01D-1251-10 g.chr3:52443574G>A KIPAN 3 52443594 52443594 + 5'Flank SNP T T C TCGA-G7-A8LE-01A-11D-A35Z-10 TCGA-G7-A8LE-10A-01D-A35Z-10 g.chr3:52443594T>C KIPAN 3 52443600 52443600 + 5'Flank SNP T T C TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr3:52443600T>C KIPAN 3 52443600 52443600 + 5'Flank SNP T T G TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr3:52443600T>G KIPAN 3 52443623 52443647 + 5'Flank DEL ACCTGCGATGAGGAAAGGAAAGCAG ACCTGCGATGAGGAAAGGAAAGCAG - TCGA-CZ-5470-01A-01D-1501-10 TCGA-CZ-5470-11A-01D-1501-10 g.chr3:52443623_52443647delACCTGCGATGAGGAAAGGAAAGCAG KIPAN 3 52443729 52443729 + 5'Flank SNP C C T TCGA-B8-5551-01A-01D-1534-10 TCGA-B8-5551-10A-01D-1535-10 g.chr3:52443729C>T KIPAN 3 52443747 52443747 + 5'Flank SNP A A G TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr3:52443747A>G KIPAN 3 52443866 52443866 + 5'Flank SNP C C G TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr3:52443866C>G KIPAN 3 52443866 52443866 + 5'Flank SNP C C T TCGA-BQ-5892-01A-11D-1589-08 TCGA-BQ-5892-11A-01D-1589-08 g.chr3:52443866C>T KIPAN 3 52443892 52443892 + 5'Flank SNP C C T TCGA-BP-4962-01A-01D-1462-08 TCGA-BP-4962-11A-01D-1462-08 g.chr3:52443892C>T KIPAN 3 52443892 52443892 + 5'Flank SNP C C T TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr3:52443892C>T KIPAN 3 52443894 52443894 + 5'Flank SNP T T C TCGA-B0-5096-01A-01D-1421-08 TCGA-B0-5096-11A-01D-1421-08 g.chr3:52443894T>C KIRC 3 52436345 52436345 + Frame_Shift_Del DEL G G - TCGA-B8-4151-01A-01D-1806-10 TCGA-B8-4151-10A-01D-1251-10 g.chr3:52436345delG c.2149delC c.(2149-2151)cggfs p.R718fs KIRC 3 52436362 52436362 + Frame_Shift_Del DEL T T - TCGA-B0-5699-01A-11D-1534-10 TCGA-B0-5699-11A-01D-1534-10 g.chr3:52436362delT c.2132delA c.(2131-2133)aagfs p.K711fs KIRC 3 52436397 52436397 + Frame_Shift_Del DEL C C - TCGA-BP-5174-01A-01D-1429-08 TCGA-BP-5174-11A-01D-1429-08 g.chr3:52436397delC c.2097delG c.(2095-2097)cggfs p.R701fs KIRC 3 52436403 52436403 + Frame_Shift_Del DEL G G - TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr3:52436403delG c.2091delC c.(2089-2091)tccfs p.S697fs KIRC 3 52437163 52437163 + Nonsense_Mutation SNP G G C TCGA-B8-4143-01A-01D-1806-10 TCGA-B8-4143-11A-01D-1251-10 g.chr3:52437163G>C c.1881C>G c.(1879-1881)taC>taG p.Y627* KIRC 3 52437168 52437168 + Nonsense_Mutation SNP T T A TCGA-CJ-4923-01A-01D-1429-08 TCGA-CJ-4923-11A-01D-1429-08 g.chr3:52437168T>A c.1876A>T c.(1876-1878)Aaa>Taa p.K626* KIRC 3 52437530 52437533 + Frame_Shift_Del DEL ATGC ATGC - TCGA-CW-6097-01A-11D-1669-08 TCGA-CW-6097-11A-01D-1669-08 g.chr3:52437530_52437533delATGC c.1628_1631delGCAT c.(1627-1632)tgcatafs p.CI543fs KIRC 3 52437782 52437782 + Nonsense_Mutation SNP G G C TCGA-B0-5095-01A-01D-1421-08 TCGA-B0-5095-11A-01D-1421-08 g.chr3:52437782G>C c.1379C>G c.(1378-1380)tCa>tGa p.S460* KIRC 3 52438499 52438499 + Frame_Shift_Del DEL T T - TCGA-CZ-5452-01A-01D-1501-10 TCGA-CZ-5452-11A-01D-1501-10 g.chr3:52438499delT c.1220delA c.(1219-1221)gatfs p.D408fs KIRC 3 52438515 52438515 + Nonsense_Mutation SNP C C A TCGA-A3-3317-01A-01D-0966-08 TCGA-A3-3317-11A-01D-0966-08 g.chr3:52438515C>A c.1204G>T c.(1204-1206)Gag>Tag p.E402* KIRC 3 52439196 52439196 + Frame_Shift_Del DEL T T - TCGA-CJ-4869-01A-02D-1429-08 TCGA-CJ-4869-11A-01D-1429-08 g.chr3:52439196delT c.1046delA c.(1045-1047)aacfs p.N349fs KIRC 3 52439219 52439238 + Frame_Shift_Del DEL GCTGCCTGGAGGCTTCACCA GCTGCCTGGAGGCTTCACCA - TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr3:52439219_52439238delGCTGCCTGGAGGCTTCACCA c.1004_1023delTGGTGAAGCCTCCAGGCAGC c.(1003-1023)gtggtgaagcctccaggcagcfs p.VVKPPGS335fs KIRC 3 52439306 52439306 + Silent SNP A A C TCGA-B0-4842-01A-02D-1421-08 TCGA-B0-4842-11A-01D-1421-08 g.chr3:52439306A>C c.936T>G c.(934-936)ggT>ggG p.G312G KIRC 3 52439311 52439311 + Splice_Site SNP C C A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr3:52439311C>A c.e11-1 KIRC 3 52439864 52439864 + Frame_Shift_Del DEL T T - TCGA-B0-4827-01A-02D-1421-08 TCGA-B0-4827-11A-01D-1421-08 g.chr3:52439864delT c.848delA c.(847-849)gagfs p.E284fs KIRC 3 52439876 52439876 + Nonsense_Mutation SNP G G T TCGA-BP-4163-01A-02D-1386-10 TCGA-BP-4163-11A-01D-1251-10 g.chr3:52439876G>T c.836C>A c.(835-837)tCa>tAa p.S279* KIRC 3 52439913 52439913 + Nonsense_Mutation SNP G G A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr3:52439913G>A c.799C>T c.(799-801)Cag>Tag p.Q267* KIRC 3 52440295 52440295 + Nonsense_Mutation SNP G G A TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr3:52440295G>A c.757C>T c.(757-759)Cag>Tag p.Q253* KIRC 3 52440367 52440367 + Missense_Mutation SNP T T G TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr3:52440367T>G c.685A>C c.(685-687)Aac>Cac p.N229H KIRC 3 52441261 52441261 + Missense_Mutation SNP A A C TCGA-CZ-5469-01A-01D-1501-10 TCGA-CZ-5469-11A-01D-1501-10 g.chr3:52441261A>C c.509T>G c.(508-510)tTt>tGt p.F170C KIRC 3 52441262 52441262 + Missense_Mutation SNP A A C TCGA-B0-5097-01A-01D-1421-08 TCGA-B0-5097-11A-01D-1421-08 g.chr3:52441262A>C c.508T>G c.(508-510)Ttt>Gtt p.F170V KIRC 3 52441304 52441304 + Nonsense_Mutation SNP G G A TCGA-CJ-4641-01A-02D-1386-10 TCGA-CJ-4641-11A-01D-1251-10 g.chr3:52441304G>A c.466C>T c.(466-468)Cag>Tag p.Q156* KIRC 3 52441418 52441418 + Missense_Mutation SNP G G C TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr3:52441418G>C c.434C>G c.(433-435)gCc>gGc p.A145G KIRC 3 52441470 52441470 + Nonsense_Mutation SNP C C A TCGA-B0-4691-01A-01D-1361-10 TCGA-B0-4691-11A-01D-1361-10 g.chr3:52441470C>A c.382G>T c.(382-384)Gga>Tga p.G128* KIRC 3 52442023 52442023 + 5'Flank SNP C C A TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chr3:52442023C>A KIRC 3 52442512 52442512 + 5'Flank SNP T T C TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr3:52442512T>C KIRC 3 52442512 52442512 + 5'Flank SNP T T C TCGA-CJ-4637-01A-02D-1386-10 TCGA-CJ-4637-11A-01D-1251-10 g.chr3:52442512T>C KIRC 3 52442521 52442521 + 5'Flank SNP T T C TCGA-AK-3451-01A-02D-1251-10 TCGA-AK-3451-10A-01D-1251-10 g.chr3:52442521T>C KIRC 3 52442523 52442523 + 5'Flank DEL A A - TCGA-CJ-5680-01A-11D-1534-10 TCGA-CJ-5680-11A-01D-1535-10 g.chr3:52442523delA KIRC 3 52442567 52442567 + 5'Flank SNP G G A TCGA-BP-4337-01A-01D-1366-10 TCGA-BP-4337-11A-01D-1366-10 g.chr3:52442567G>A KIRC 3 52442600 52442600 + 5'Flank SNP G G C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr3:52442600G>C KIRC 3 52443568 52443568 + 5'Flank SNP A A G TCGA-CJ-4636-01A-02D-1386-10 TCGA-CJ-4636-11A-01D-1251-10 g.chr3:52443568A>G KIRC 3 52443568 52443568 + 5'Flank SNP A A T TCGA-CZ-4866-01A-01D-1501-10 TCGA-CZ-4866-11A-01D-1501-10 g.chr3:52443568A>T KIRC 3 52443574 52443574 + 5'Flank SNP G G A TCGA-CJ-4638-01A-02D-1386-10 TCGA-CJ-4638-11A-01D-1251-10 g.chr3:52443574G>A KIRC 3 52443600 52443600 + 5'Flank SNP T T G TCGA-CJ-4882-01A-02D-1429-08 TCGA-CJ-4882-11A-01D-1429-08 g.chr3:52443600T>G KIRC 3 52443623 52443647 + 5'Flank DEL ACCTGCGATGAGGAAAGGAAAGCAG ACCTGCGATGAGGAAAGGAAAGCAG - TCGA-CZ-5470-01A-01D-1501-10 TCGA-CZ-5470-11A-01D-1501-10 g.chr3:52443623_52443647delACCTGCGATGAGGAAAGGAAAGCAG KIRC 3 52443729 52443729 + 5'Flank SNP C C T TCGA-B8-5551-01A-01D-1534-10 TCGA-B8-5551-10A-01D-1535-10 g.chr3:52443729C>T KIRC 3 52443747 52443747 + 5'Flank SNP A A G TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr3:52443747A>G KIRC 3 52443866 52443866 + 5'Flank SNP C C G TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr3:52443866C>G KIRC 3 52443892 52443892 + 5'Flank SNP C C T TCGA-BP-4962-01A-01D-1462-08 TCGA-BP-4962-11A-01D-1462-08 g.chr3:52443892C>T KIRC 3 52443892 52443892 + 5'Flank SNP C C T TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr3:52443892C>T KIRC 3 52443894 52443894 + 5'Flank SNP T T C TCGA-B0-5096-01A-01D-1421-08 TCGA-B0-5096-11A-01D-1421-08 g.chr3:52443894T>C KIRP 3 52437652 52437652 + Frame_Shift_Del DEL G G - TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr3:52437652delG c.1509delC c.(1507-1509)ttcfs p.F503fs KIRP 3 52437657 52437657 + Missense_Mutation SNP C C G TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr3:52437657C>G c.1504G>C c.(1504-1506)Gct>Cct p.A502P KIRP 3 52437709 52437709 + Frame_Shift_Del DEL G G - TCGA-G7-A8LD-01A-11D-A35Z-10 TCGA-G7-A8LD-10A-01D-A35Z-10 g.chr3:52437709delG c.1452delC c.(1450-1452)cccfs p.P484fs KIRP 3 52437846 52437846 + Missense_Mutation SNP C C A TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr3:52437846C>A c.1315G>T c.(1315-1317)Gtg>Ttg p.V439L KIRP 3 52437889 52437889 + Frame_Shift_Del DEL C C - TCGA-AL-3473-01A-01D-1252-08 TCGA-AL-3473-10A-01D-1252-08 g.chr3:52437889delC c.1272delG c.(1270-1272)gggfs p.G424fs KIRP 3 52439133 52439133 + Missense_Mutation SNP G G T TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr3:52439133G>T c.1109C>A c.(1108-1110)cCc>cAc p.P370H KIRP 3 52439271 52439271 + Frame_Shift_Del DEL G G - TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr3:52439271delG c.971delC c.(970-972)ccafs p.P324fs KIRP 3 52439275 52439275 + Missense_Mutation SNP C C A TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr3:52439275C>A c.967G>T c.(967-969)Gcc>Tcc p.A323S KIRP 3 52439781 52439781 + Splice_Site SNP C C A TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr3:52439781C>A c.931G>T c.(931-933)Gat>Tat p.D311Y KIRP 3 52439900 52439900 + Missense_Mutation SNP A A G TCGA-BQ-5877-01A-11D-1589-08 TCGA-BQ-5877-11A-01D-1589-08 g.chr3:52439900A>G c.812T>C c.(811-813)aTt>aCt p.I271T KIRP 3 52441190 52441190 + Splice_Site SNP C C T TCGA-BQ-5875-01A-11D-1589-08 TCGA-BQ-5875-11A-01D-1589-08 g.chr3:52441190C>T c.580G>A c.(580-582)Ggg>Agg p.G194R KIRP 3 52441229 52441230 + Frame_Shift_Del DEL AG AG - TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr3:52441229_52441230delAG c.540_541delCT c.(538-543)ctctttfs p.F181fs KIRP 3 52441417 52441417 + Silent SNP G G C TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr3:52441417G>C c.435C>G c.(433-435)gcC>gcG p.A145A KIRP 3 52443594 52443594 + 5'Flank SNP T T C TCGA-G7-A8LE-01A-11D-A35Z-10 TCGA-G7-A8LE-10A-01D-A35Z-10 g.chr3:52443594T>C KIRP 3 52443600 52443600 + 5'Flank SNP T T C TCGA-2Z-A9J2-01A-11D-A382-10 TCGA-2Z-A9J2-10A-01D-A385-10 g.chr3:52443600T>C KIRP 3 52443866 52443866 + 5'Flank SNP C C T TCGA-BQ-5892-01A-11D-1589-08 TCGA-BQ-5892-11A-01D-1589-08 g.chr3:52443866C>T LIHC 3 52436363 52436363 + Nonsense_Mutation SNP T T A TCGA-DD-AAVR-01A-11D-A40R-10 TCGA-DD-AAVR-10A-01D-A40U-10 g.chr3:52436363T>A c.2131A>T c.(2131-2133)Aag>Tag p.K711* LIHC 3 52436639 52436640 + Frame_Shift_Ins INS - - A TCGA-ED-A7PX-01A-51D-A34Z-10 TCGA-ED-A7PX-10A-01D-A34Z-10 g.chr3:52436639_52436640insA c.2034_2035insT c.(2032-2037)tttatcfs p.I679fs LIHC 3 52436677 52436708 + Splice_Site DEL CTCTGGTCATCAATCTGTAGGAGAGAAGAAGA CTCTGGTCATCAATCTGTAGGAGAGAAGAAGA - TCGA-2Y-A9H3-01A-11D-A382-10 TCGA-2Y-A9H3-10A-01D-A385-10 g.chr3:52436677_52436708delCTCTGGTCATCAATCTGTAGGAGAGAAGAAGA c.1984_1997delTCTTCTTCTCTCCTACAGATTGATGACCAGAG c.(1984-1998)tcttcttctctccta>a p.SSSLL662fs LIHC 3 52436687 52436688 + Frame_Shift_Ins INS - - A TCGA-BC-A10R-01A-11D-A12Z-10 TCGA-BC-A10R-11A-11D-A12Z-10 g.chr3:52436687_52436688insA c.1986_1987insT c.(1984-1989)attgatfs p.D663fs LIHC 3 52437456 52437456 + Frame_Shift_Del DEL C C - TCGA-CC-5260-01A-01D-A12Z-10 TCGA-CC-5260-10B-01D-A12Z-10 g.chr3:52437456delC c.1705delG c.(1705-1707)gtgfs p.V569fs LIHC 3 52437545 52437545 + Missense_Mutation SNP A A T TCGA-ZS-A9CG-01A-11D-A36X-10 TCGA-ZS-A9CG-10A-01D-A370-10 g.chr3:52437545A>T c.1616T>A c.(1615-1617)cTg>cAg p.L539Q LIHC 3 52437795 52437795 + Nonsense_Mutation SNP G G A TCGA-DD-AADA-01A-11D-A40R-10 TCGA-DD-AADA-10A-01D-A40U-10 g.chr3:52437795G>A c.1366C>T c.(1366-1368)Cag>Tag p.Q456* LIHC 3 52437802 52437803 + Frame_Shift_Del DEL TT TT - TCGA-WQ-A9G7-01A-11D-A36X-10 TCGA-WQ-A9G7-10A-01D-A370-10 g.chr3:52437802_52437803delTT c.1358_1359delAA c.(1357-1359)aaafs p.K453fs LIHC 3 52437901 52437901 + Frame_Shift_Del DEL C C - TCGA-DD-AA3A-01A-11D-A36X-10 TCGA-DD-AA3A-10A-01D-A370-10 g.chr3:52437901delC c.1260delG c.(1258-1260)gggfs p.G420fs LIHC 3 52439158 52439167 + Frame_Shift_Del DEL CTAGAAAGGC CTAGAAAGGC - TCGA-2Y-A9H2-01A-12D-A382-10 TCGA-2Y-A9H2-10A-01D-A385-10 g.chr3:52439158_52439167delCTAGAAAGGC c.1075_1084delGCCTTTCTAG c.(1075-1086)gcctttctagacfs p.AFLD359fs LIHC 3 52439294 52439294 + Silent SNP C C T TCGA-DD-AADF-01A-11D-A40R-10 TCGA-DD-AADF-10A-01D-A40U-10 g.chr3:52439294C>T c.948G>A c.(946-948)gcG>gcA p.A316A LIHC 3 52439874 52439874 + Nonsense_Mutation SNP G G A TCGA-G3-A25T-01A-11D-A16V-10 TCGA-G3-A25T-10A-01D-A16V-10 g.chr3:52439874G>A c.838C>T c.(838-840)Cag>Tag p.Q280* LIHC 3 52440270 52440276 + Splice_Site DEL TGCTGCA TGCTGCA - TCGA-DD-A1EF-01A-11D-A12Z-10 TCGA-DD-A1EF-10A-01D-A12Z-10 g.chr3:52440270_52440276delTGCTGCA c.776_782delTGCAGCA c.(775-783)ctgcagcag>cg p.LQQ259fs LIHC 3 52440295 52440295 + Nonsense_Mutation SNP G G A TCGA-DD-A118-01A-11D-A12Z-10 TCGA-DD-A118-11A-11D-A12Z-10 g.chr3:52440295G>A c.757C>T c.(757-759)Cag>Tag p.Q253* LIHC 3 52440340 52440348 + In_Frame_Del DEL TGCGGTCGG TGCGGTCGG - TCGA-BC-A10Q-01A-11D-A12Z-10 TCGA-BC-A10Q-11A-11D-A12Z-10 g.chr3:52440340_52440348delTGCGGTCGG c.704_712delCCGACCGCA c.(703-714)cccgaccgcagg>cgg p.PDR235del LIHC 3 52440899 52440899 + Missense_Mutation SNP C C A TCGA-2Y-A9GU-01A-11D-A382-10 TCGA-2Y-A9GU-10A-01D-A385-10 g.chr3:52440899C>A c.605G>T c.(604-606)tGg>tTg p.W202L LIHC 3 52440918 52440918 + Missense_Mutation SNP A A C TCGA-DD-A4NA-01A-11D-A25V-10 TCGA-DD-A4NA-11A-11D-A25V-10 g.chr3:52440918A>C c.586T>G c.(586-588)Tgg>Ggg p.W196G LIHC 3 52441262 52441262 + Missense_Mutation SNP A A C TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr3:52441262A>C c.508T>G c.(508-510)Ttt>Gtt p.F170V LIHC 3 52441263 52441263 + Missense_Mutation SNP G G C TCGA-DD-A73G-01A-22D-A32G-10 TCGA-DD-A73G-10A-01D-A32G-10 g.chr3:52441263G>C c.507C>G c.(505-507)caC>caG p.H169Q LIHC 3 52441304 52441304 + Nonsense_Mutation SNP G G A TCGA-DD-AADA-01A-11D-A40R-10 TCGA-DD-AADA-10A-01D-A40U-10 g.chr3:52441304G>A c.466C>T c.(466-468)Cag>Tag p.Q156* LIHC 3 52441334 52441334 + Splice_Site SNP T T A TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr3:52441334T>A c.e7-2 LIHC 3 52442000 52442062 + 5'Flank DEL CCTTCATGCGACTCAGGGTGGGTCCCAGGTCCACGCTGCTGCAGTTCAGGAGCACGCTCAGCA CCTTCATGCGACTCAGGGTGGGTCCCAGGTCCACGCTGCTGCAGTTCAGGAGCACGCTCAGCA - TCGA-FV-A3I0-01A-11D-A22F-10 TCGA-FV-A3I0-11A-11D-A22F-10 g.chr3:52442000_52442062delCCTTCATGCGACTCAGGGTGGGTCCCAGGTCCACGCTGCTGCAGTTCAGGAGCACGCTCAGCA LIHC 3 52442001 52442005 + 5'Flank DEL CTTCA CTTCA - TCGA-2Y-A9H6-01A-11D-A38X-10 TCGA-2Y-A9H6-10A-01D-A38X-10 g.chr3:52442001_52442005delCTTCA LIHC 3 52442612 52442612 + 5'Flank SNP C C T TCGA-DD-AAVR-01A-11D-A40R-10 TCGA-DD-AAVR-10A-01D-A40U-10 g.chr3:52442612C>T LUAD 3 52436883 52436883 + Missense_Mutation SNP A A G TCGA-97-A4M6-01A-11D-A24P-08 TCGA-97-A4M6-10A-01D-A24P-08 g.chr3:52436883A>G c.1895T>C c.(1894-1896)cTg>cCg p.L632P LUAD 3 52437152 52437152 + Splice_Site SNP A A G TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr3:52437152A>G c.e14+1 LUAD 3 52437180 52437180 + Missense_Mutation SNP A A T TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr3:52437180A>T c.1864T>A c.(1864-1866)Ttg>Atg p.L622M LUAD 3 52437181 52437181 + Silent SNP G G A TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr3:52437181G>A c.1863C>T c.(1861-1863)ccC>ccT p.P621P LUAD 3 52437500 52437500 + Frame_Shift_Del DEL C C - TCGA-95-7948-01A-11D-2184-08 TCGA-95-7948-10A-01D-2184-08 g.chr3:52437500delC c.1661delG c.(1660-1662)ggtfs p.G554fs LUAD 3 52437782 52437782 + Nonsense_Mutation SNP G G C TCGA-97-A4LX-01A-11D-A24P-08 TCGA-97-A4LX-10A-01D-A24P-08 g.chr3:52437782G>C c.1379C>G c.(1378-1380)tCa>tGa p.S460* LUAD 3 52439224 52439224 + Missense_Mutation SNP C C T TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr3:52439224C>T c.1018G>A c.(1018-1020)Ggc>Agc p.G340S LUAD 3 52441235 52441235 + Missense_Mutation SNP G G A TCGA-49-4510-01A-01D-1265-08 TCGA-49-4510-11A-01D-1265-08 g.chr3:52441235G>A c.535C>T c.(535-537)Cgg>Tgg p.R179W LUAD 3 52442491 52442491 + 5'Flank SNP T T C TCGA-97-A4M0-01A-11D-A24P-08 TCGA-97-A4M0-10A-01D-A24P-08 g.chr3:52442491T>C LUAD 3 52442492 52442492 + 5'Flank SNP G G A TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr3:52442492G>A LUSC 3 52440372 52440372 + Missense_Mutation SNP C C T TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chr3:52440372C>T c.680G>A c.(679-681)cGc>cAc p.R227H LUSC 3 52443746 52443746 + 5'Flank SNP C C A TCGA-60-2708-01A-01D-1522-08 TCGA-60-2708-11A-01D-1522-08 g.chr3:52443746C>A OV 3 52440373 52440373 + Missense_Mutation SNP G G A TCGA-13-0714-01A-01W-0370-10 TCGA-13-0714-10B-01W-0370-10 g.chr3:52440373G>A c.679C>T c.(679-681)Cgc>Tgc p.R227C PAAD 3 52439281 52439281 + Missense_Mutation SNP C C T TCGA-FB-AAQ0-01A-31D-A40W-08 TCGA-FB-AAQ0-11A-11D-A40W-08 g.chr3:52439281C>T c.961G>A c.(961-963)Gca>Aca p.A321T PAAD 3 52439312 52439312 + Splice_Site SNP T T G TCGA-FZ-5922-01A-11D-1609-08 TCGA-FZ-5922-11A-01D-1609-08 g.chr3:52439312T>G c.e11-2 PRAD 3 52437772 52437772 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:52437772C>T c.1389G>A c.(1387-1389)ctG>ctA p.L463L READ 3 52436345 52436345 + Missense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:52436345G>A c.2149C>T c.(2149-2151)Cgg>Tgg p.R717W READ 3 52436805 52436805 + Missense_Mutation SNP T T C TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr3:52436805T>C c.1973A>G c.(1972-1974)aAg>aGg p.K658R SARC 3 52438591 52438591 + Silent SNP G G A TCGA-SI-AA8B-01A-11D-A387-09 TCGA-SI-AA8B-10A-01D-A38A-09 g.chr3:52438591G>A c.1128C>T c.(1126-1128)gaC>gaT p.D376D SKCM 3 52437159 52437159 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr3:52437159G>A c.1885C>T c.(1885-1887)Ccc>Tcc p.P629S SKCM 3 52438469 52438469 + Splice_Site SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr3:52438469C>A c.1250G>T c.(1249-1251)aGg>aTg p.R417M SKCM 3 52438473 52438473 + Missense_Mutation SNP G G A TCGA-EE-A2A5-06A-11D-A197-08 TCGA-EE-A2A5-10A-01D-A199-08 g.chr3:52438473G>A c.1246C>T c.(1246-1248)Ctt>Ttt p.L416F SKCM 3 52439273 52439273 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:52439273G>A c.969C>T c.(967-969)gcC>gcT p.A323A SKCM 3 52441424 52441424 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:52441424C>T c.428G>A c.(427-429)aGc>aAc p.S143N SKCM 3 52441477 52441477 + Splice_Site SNP C C T TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr3:52441477C>T c.e6-1 SKCM 3 52442559 52442559 + 5'Flank SNP G G A TCGA-FS-A4FD-06A-11D-A25O-08 TCGA-FS-A4FD-10B-01D-A25O-08 g.chr3:52442559G>A SKCM 3 52442570 52442570 + 5'Flank SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr3:52442570G>A SKCM 3 52442571 52442571 + 5'Flank SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr3:52442571G>A SKCM 3 52443604 52443604 + 5'Flank SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr3:52443604C>T ACC 1 185069018 185069018 + Nonsense_Mutation SNP C C G TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr1:185069018C>G c.833C>G c.(832-834)tCa>tGa p.S278* BLCA 1 185056735 185056735 + Nonsense_Mutation SNP G G A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr1:185056735G>A c.50G>A c.(49-51)tGg>tAg p.W17* BLCA 1 185056770 185056770 + Nonsense_Mutation SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr1:185056770C>T c.85C>T c.(85-87)Cag>Tag p.Q29* BLCA 1 185067233 185067233 + Missense_Mutation SNP A A G TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr1:185067233A>G c.494A>G c.(493-495)gAa>gGa p.E165G BLCA 1 185067380 185067380 + Missense_Mutation SNP T T A TCGA-DK-AA6Q-01A-11D-A391-08 TCGA-DK-AA6Q-10A-01D-A394-08 g.chr1:185067380T>A c.641T>A c.(640-642)aTg>aAg p.M214K BLCA 1 185069351 185069351 + Missense_Mutation SNP C C T TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr1:185069351C>T c.929C>T c.(928-930)tCt>tTt p.S310F BRCA 1 185060751 185060751 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:185060751G>A c.128G>A c.(127-129)cGa>cAa p.R43Q BRCA 1 185060756 185060756 + Silent SNP C C T TCGA-A2-A0SW-01A-11D-A099-09 TCGA-A2-A0SW-10A-01W-A097-09 g.chr1:185060756C>T c.133C>T c.(133-135)Cta>Tta p.L45L BRCA 1 185062237 185062237 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr1:185062237G>T c.293G>T c.(292-294)aGa>aTa p.R98I BRCA 1 185067212 185067212 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:185067212G>A c.473G>A c.(472-474)cGa>cAa p.R158Q CESC 1 185069364 185069364 + Silent SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr1:185069364C>T c.942C>T c.(940-942)gtC>gtT p.V314V COAD 1 185062283 185062283 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:185062283T>G c.339T>G c.(337-339)atT>atG p.I113M COAD 1 185062312 185062312 + Missense_Mutation SNP A A C TCGA-AA-A00Z-01A-01W-A005-10 TCGA-AA-A00Z-10A-01W-A005-10 g.chr1:185062312A>C c.368A>C c.(367-369)cAt>cCt p.H123P COAD 1 185067316 185067316 + Missense_Mutation SNP A A T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr1:185067316A>T c.577A>T c.(577-579)Agt>Tgt p.S193C COAD 1 185067326 185067326 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr1:185067326G>A c.587G>A c.(586-588)cGg>cAg p.R196Q COAD 1 185069346 185069346 + Frame_Shift_Del DEL T T - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:185069346delT c.924delT c.(922-924)tctfs p.S308fs COADREAD 1 185056762 185056762 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:185056762G>A c.77G>A c.(76-78)cGa>cAa p.R26Q COADREAD 1 185062283 185062283 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr1:185062283T>G c.339T>G c.(337-339)atT>atG p.I113M COADREAD 1 185062312 185062312 + Missense_Mutation SNP A A C TCGA-AA-A00Z-01A-01W-A005-10 TCGA-AA-A00Z-10A-01W-A005-10 g.chr1:185062312A>C c.368A>C c.(367-369)cAt>cCt p.H123P COADREAD 1 185067316 185067316 + Missense_Mutation SNP A A T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr1:185067316A>T c.577A>T c.(577-579)Agt>Tgt p.S193C COADREAD 1 185067326 185067326 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr1:185067326G>A c.587G>A c.(586-588)cGg>cAg p.R196Q COADREAD 1 185069002 185069002 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:185069002C>T c.817C>T c.(817-819)Cga>Tga p.R273* COADREAD 1 185069346 185069346 + Frame_Shift_Del DEL T T - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:185069346delT c.924delT c.(922-924)tctfs p.S308fs ESCA 1 185069041 185069041 + Missense_Mutation SNP G G A TCGA-L5-A8NF-01A-11D-A37C-09 TCGA-L5-A8NF-11A-11D-A37F-09 g.chr1:185069041G>A c.856G>A c.(856-858)Gcc>Acc p.A286T GBM 1 185069006 185069006 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 g.chr1:185069006G>A c.821G>A c.(820-822)aGc>aAc p.S274N GBMLGG 1 185067296 185067296 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:185067296G>T c.557G>T c.(556-558)aGc>aTc p.S186I GBMLGG 1 185067376 185067376 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:185067376G>T c.637G>T c.(637-639)Gca>Tca p.A213S GBMLGG 1 185069006 185069006 + Missense_Mutation SNP G G A TCGA-06-5411-01A-01D-1696-08 TCGA-06-5411-10A-01D-1696-08 g.chr1:185069006G>A c.821G>A c.(820-822)aGc>aAc p.S274N HNSC 1 185062311 185062311 + Missense_Mutation SNP C C A TCGA-QK-A6VC-01A-23D-A34J-08 TCGA-QK-A6VC-10B-01D-A34M-08 g.chr1:185062311C>A c.367C>A c.(367-369)Cat>Aat p.H123N HNSC 1 185062311 185062311 + Missense_Mutation SNP C C T TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr1:185062311C>T c.367C>T c.(367-369)Cat>Tat p.H123Y LGG 1 185067296 185067296 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:185067296G>T c.557G>T c.(556-558)aGc>aTc p.S186I LGG 1 185067376 185067376 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:185067376G>T c.637G>T c.(637-639)Gca>Tca p.A213S LUAD 1 185060780 185060780 + Missense_Mutation SNP A A T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr1:185060780A>T c.157A>T c.(157-159)Att>Ttt p.I53F LUAD 1 185068982 185068982 + Missense_Mutation SNP G G A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr1:185068982G>A c.797G>A c.(796-798)aGg>aAg p.R266K LUAD 1 185069342 185069342 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr1:185069342G>T c.920G>T c.(919-921)gGc>gTc p.G307V READ 1 185056762 185056762 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:185056762G>A c.77G>A c.(76-78)cGa>cAa p.R26Q READ 1 185069002 185069002 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr1:185069002C>T c.817C>T c.(817-819)Cga>Tga p.R273* SKCM 1 185056719 185056719 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr1:185056719C>T c.34C>T c.(34-36)Cca>Tca p.P12S SKCM 1 185062302 185062302 + Missense_Mutation SNP T T C TCGA-D3-A1Q1-06A-21D-A196-08 TCGA-D3-A1Q1-10A-01D-A198-08 g.chr1:185062302T>C c.358T>C c.(358-360)Tat>Cat p.Y120H

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 1 185056735 185056735 single base substitution G A exon_variant BLCA-US 1 185056735 185056735 single base substitution G A stop_gained W17* 50G>A BRCA-EU 1 185009524 185009524 single base substitution A T upstream_gene_variant BRCA-EU 1 185009590 185009590 single base substitution T A upstream_gene_variant BRCA-EU 1 185009734 185009734 single base substitution A C upstream_gene_variant BRCA-EU 1 185011180 185011180 single base substitution T A upstream_gene_variant BRCA-EU 1 185013098 185013098 single base substitution C T upstream_gene_variant BRCA-EU 1 185014270 185014270 single base substitution C G upstream_gene_variant BRCA-EU 1 185014590 185014590 single base substitution C T 5_prime_UTR_variant BRCA-EU 1 185014590 185014590 single base substitution C T upstream_gene_variant BRCA-EU 1 185015153 185015153 single base substitution C T intron_variant BRCA-EU 1 185015153 185015153 single base substitution C T upstream_gene_variant BRCA-EU 1 185016127 185016127 deletion of <=200bp T - intron_variant BRCA-EU 1 185016911 185016921 deletion of <=200bp AGAAAAATAAG - intron_variant BRCA-EU 1 185017481 185017481 single base substitution G C intron_variant BRCA-EU 1 185018335 185018335 single base substitution C T intron_variant BRCA-EU 1 185018900 185018900 single base substitution G T intron_variant BRCA-EU 1 185019064 185019064 deletion of <=200bp C - intron_variant BRCA-EU 1 185020005 185020005 single base substitution C G intron_variant BRCA-EU 1 185020278 185020278 deletion of <=200bp A - intron_variant BRCA-EU 1 185020374 185020374 single base substitution G A intron_variant BRCA-EU 1 185020377 185020377 single base substitution T G intron_variant BRCA-EU 1 185020608 185020608 single base substitution C G intron_variant BRCA-EU 1 185021008 185021008 insertion of <=200bp - A intron_variant BRCA-EU 1 185021432 185021432 deletion of <=200bp A - intron_variant BRCA-EU 1 185021780 185021780 single base substitution C T intron_variant BRCA-EU 1 185021781 185021781 single base substitution G A intron_variant BRCA-EU 1 185023128 185023128 deletion of <=200bp C - intron_variant BRCA-EU 1 185023304 185023304 single base substitution A C intron_variant BRCA-EU 1 185023627 185023627 single base substitution C T intron_variant BRCA-EU 1 185024669 185024669 single base substitution C G intron_variant BRCA-EU 1 185024695 185024695 single base substitution C T intron_variant BRCA-EU 1 185024840 185024840 single base substitution G A intron_variant BRCA-EU 1 185025495 185025495 single base substitution T C intron_variant BRCA-EU 1 185026578 185026578 deletion of <=200bp T - intron_variant BRCA-EU 1 185027938 185027938 single base substitution A T intron_variant BRCA-EU 1 185028164 185028164 single base substitution C G intron_variant BRCA-EU 1 185028390 185028390 single base substitution C G intron_variant BRCA-EU 1 185029064 185029064 single base substitution C T intron_variant BRCA-EU 1 185030344 185030344 single base substitution C G intron_variant BRCA-EU 1 185030376 185030376 single base substitution C T intron_variant BRCA-EU 1 185030504 185030504 deletion of <=200bp A - intron_variant BRCA-EU 1 185030504 185030504 single base substitution A G intron_variant BRCA-EU 1 185030565 185030565 insertion of <=200bp - A intron_variant BRCA-EU 1 185030740 185030740 single base substitution C T intron_variant BRCA-EU 1 185031909 185031909 single base substitution C G intron_variant BRCA-EU 1 185032001 185032001 single base substitution G C intron_variant BRCA-EU 1 185032033 185032033 single base substitution C T intron_variant BRCA-EU 1 185033359 185033359 single base substitution C G intron_variant BRCA-EU 1 185033981 185033981 insertion of <=200bp - T intron_variant BRCA-EU 1 185035999 185035999 insertion of <=200bp - T intron_variant BRCA-EU 1 185038117 185038117 deletion of <=200bp T - intron_variant BRCA-EU 1 185038372 185038372 single base substitution C G intron_variant BRCA-EU 1 185039149 185039149 single base substitution T C intron_variant BRCA-EU 1 185040019 185040019 single base substitution C T intron_variant BRCA-EU 1 185040220 185040220 single base substitution G C intron_variant BRCA-EU 1 185040826 185040826 single base substitution C T intron_variant BRCA-EU 1 185041151 185041151 single base substitution T G intron_variant BRCA-EU 1 185042698 185042698 deletion of <=200bp T - intron_variant BRCA-EU 1 185043280 185043280 single base substitution G A intron_variant BRCA-EU 1 185043814 185043814 deletion of <=200bp A - intron_variant BRCA-EU 1 185045995 185045995 deletion of <=200bp T - intron_variant BRCA-EU 1 185046313 185046313 single base substitution T A intron_variant BRCA-EU 1 185046716 185046716 single base substitution C T intron_variant BRCA-EU 1 185047386 185047386 single base substitution T G intron_variant BRCA-EU 1 185047698 185047698 single base substitution G A intron_variant BRCA-EU 1 185048577 185048577 single base substitution C G intron_variant BRCA-EU 1 185048934 185048934 single base substitution G A intron_variant BRCA-EU 1 185049986 185049986 single base substitution G C intron_variant BRCA-EU 1 185050183 185050183 single base substitution G C intron_variant BRCA-EU 1 185050514 185050514 single base substitution C A intron_variant BRCA-EU 1 185050654 185050654 single base substitution T C intron_variant BRCA-EU 1 185051068 185051068 insertion of <=200bp - T intron_variant BRCA-EU 1 185051199 185051199 single base substitution C T intron_variant BRCA-EU 1 185054797 185054797 single base substitution T C intron_variant BRCA-EU 1 185055202 185055202 deletion of <=200bp T - intron_variant BRCA-EU 1 185055428 185055428 single base substitution G A intron_variant BRCA-EU 1 185055493 185055493 deletion of <=200bp T - intron_variant BRCA-EU 1 185056292 185056292 single base substitution C G intron_variant BRCA-EU 1 185056314 185056314 deletion of <=200bp A - intron_variant BRCA-EU 1 185056482 185056482 single base substitution C G intron_variant BRCA-EU 1 185057933 185057933 single base substitution T C intron_variant BRCA-EU 1 185058102 185058102 single base substitution T C intron_variant BRCA-EU 1 185058212 185058212 single base substitution G A intron_variant BRCA-EU 1 185059063 185059063 deletion of <=200bp T - intron_variant BRCA-EU 1 185059197 185059197 single base substitution G T intron_variant BRCA-EU 1 185060794 185060794 single base substitution G A exon_variant BRCA-EU 1 185060794 185060794 single base substitution G A missense_variant M57I 171G>A BRCA-EU 1 185061357 185061357 single base substitution G A downstream_gene_variant BRCA-EU 1 185061357 185061357 single base substitution G A intron_variant BRCA-EU 1 185061460 185061460 single base substitution C T downstream_gene_variant BRCA-EU 1 185061460 185061460 single base substitution C T intron_variant BRCA-EU 1 185061972 185061972 insertion of <=200bp - T downstream_gene_variant BRCA-EU 1 185061972 185061972 insertion of <=200bp - T intron_variant BRCA-EU 1 185063617 185063617 single base substitution C T downstream_gene_variant BRCA-EU 1 185063617 185063617 single base substitution C T intron_variant BRCA-EU 1 185064166 185064166 single base substitution C G downstream_gene_variant BRCA-EU 1 185064166 185064166 single base substitution C G intron_variant BRCA-EU 1 185064498 185064498 single base substitution C A downstream_gene_variant BRCA-EU 1 185064498 185064498 single base substitution C A intron_variant BRCA-EU 1 185064614 185064614 single base substitution T C downstream_gene_variant BRCA-EU 1 185064614 185064614 single base substitution T C intron_variant BRCA-EU 1 185065736 185065736 single base substitution T C downstream_gene_variant BRCA-EU 1 185065736 185065736 single base substitution T C intron_variant BRCA-EU 1 185066959 185066959 single base substitution G T intron_variant BRCA-EU 1 185067325 185067325 single base substitution C T missense_variant R124W 370C>T BRCA-EU 1 185067325 185067325 single base substitution C T missense_variant R196W 586C>T BRCA-EU 1 185067640 185067640 single base substitution G A intron_variant BRCA-EU 1 185068779 185068779 single base substitution G A intron_variant BRCA-EU 1 185069236 185069236 deletion of <=200bp A - downstream_gene_variant BRCA-EU 1 185069236 185069236 deletion of <=200bp A - intron_variant BRCA-EU 1 185070765 185070765 single base substitution A G 3_prime_UTR_variant BRCA-EU 1 185070765 185070765 single base substitution A G downstream_gene_variant BRCA-EU 1 185070884 185070884 single base substitution C T 3_prime_UTR_variant BRCA-EU 1 185070884 185070884 single base substitution C T downstream_gene_variant BRCA-EU 1 185071190 185071190 single base substitution G C 3_prime_UTR_variant BRCA-EU 1 185071190 185071190 single base substitution G C downstream_gene_variant BRCA-EU 1 185072067 185072067 single base substitution G A downstream_gene_variant BRCA-EU 1 185072510 185072510 insertion of <=200bp - T downstream_gene_variant BRCA-EU 1 185074005 185074005 single base substitution A G downstream_gene_variant BRCA-EU 1 185074413 185074413 single base substitution C A downstream_gene_variant BRCA-EU 1 185074625 185074625 single base substitution C G downstream_gene_variant BRCA-EU 1 185074725 185074725 single base substitution C T downstream_gene_variant BRCA-EU 1 185076616 185076616 single base substitution C G downstream_gene_variant BRCA-FR 1 185011422 185011422 single base substitution G A upstream_gene_variant BRCA-FR 1 185015153 185015153 single base substitution C T intron_variant BRCA-FR 1 185015153 185015153 single base substitution C T upstream_gene_variant BRCA-FR 1 185018900 185018900 single base substitution G T intron_variant BRCA-FR 1 185020164 185020164 single base substitution C T intron_variant BRCA-FR 1 185024669 185024669 single base substitution C G intron_variant BRCA-FR 1 185030376 185030376 single base substitution C T intron_variant BRCA-FR 1 185033359 185033359 single base substitution C G intron_variant BRCA-FR 1 185034794 185034794 single base substitution G A intron_variant BRCA-FR 1 185036430 185036430 single base substitution A C intron_variant BRCA-FR 1 185043280 185043280 single base substitution G A intron_variant BRCA-FR 1 185049986 185049986 single base substitution G C intron_variant BRCA-FR 1 185051199 185051199 single base substitution C T intron_variant BRCA-FR 1 185054797 185054797 single base substitution T C intron_variant BRCA-FR 1 185055428 185055428 single base substitution G A intron_variant BRCA-FR 1 185056482 185056482 single base substitution C G intron_variant BRCA-FR 1 185061794 185061794 single base substitution T C downstream_gene_variant BRCA-FR 1 185061794 185061794 single base substitution T C intron_variant BRCA-FR 1 185074725 185074725 single base substitution C T downstream_gene_variant BRCA-UK 1 185032001 185032001 single base substitution G C intron_variant BRCA-UK 1 185043086 185043086 single base substitution C T intron_variant BRCA-UK 1 185046313 185046313 single base substitution T A intron_variant BRCA-UK 1 185062319 185062319 single base substitution G C downstream_gene_variant BRCA-UK 1 185062319 185062319 single base substitution G C intron_variant BRCA-UK 1 185062319 185062319 single base substitution G C missense_variant E125D 375G>C BRCA-UK 1 185064498 185064498 single base substitution C A downstream_gene_variant BRCA-UK 1 185064498 185064498 single base substitution C A intron_variant BRCA-UK 1 185072067 185072067 single base substitution G A downstream_gene_variant BRCA-US 1 185060751 185060751 single base substitution G A exon_variant BRCA-US 1 185060751 185060751 single base substitution G A missense_variant R43Q 128G>A BRCA-US 1 185060756 185060756 single base substitution C T exon_variant BRCA-US 1 185060756 185060756 single base substitution C T synonymous_variant L45L 133C>T BRCA-US 1 185062237 185062237 single base substitution G T downstream_gene_variant BRCA-US 1 185062237 185062237 single base substitution G T intron_variant BRCA-US 1 185062237 185062237 single base substitution G T missense_variant R98I 293G>T BRCA-US 1 185067212 185067212 single base substitution G A missense_variant R158Q 473G>A BRCA-US 1 185067212 185067212 single base substitution G A missense_variant R86Q 257G>A BTCA-JP 1 185069373 185069373 single base substitution A G downstream_gene_variant BTCA-JP 1 185069373 185069373 single base substitution A G synonymous_variant K245K 735A>G BTCA-JP 1 185069373 185069373 single base substitution A G synonymous_variant K317K 951A>G BTCA-JP 1 185069480 185069480 single base substitution C A 3_prime_UTR_variant BTCA-JP 1 185069480 185069480 single base substitution C A downstream_gene_variant CESC-US 1 185069364 185069364 single base substitution C T downstream_gene_variant CESC-US 1 185069364 185069364 single base substitution C T synonymous_variant V242V 726C>T CESC-US 1 185069364 185069364 single base substitution C T synonymous_variant V314V 942C>T CLLE-ES 1 185068864 185068864 single base substitution G A intron_variant COAD-US 1 185067326 185067326 single base substitution G A missense_variant R124Q 371G>A COAD-US 1 185067326 185067326 single base substitution G A missense_variant R196Q 587G>A COAD-US 1 185069346 185069346 deletion of <=200bp T - downstream_gene_variant COAD-US 1 185069346 185069346 deletion of <=200bp T - frameshift_variant S236 COAD-US 1 185069346 185069346 deletion of <=200bp T - frameshift_variant S308 COCA-CN 1 185056762 185056762 single base substitution G A exon_variant COCA-CN 1 185056762 185056762 single base substitution G A missense_variant R26Q 77G>A ESAD-UK 1 185010034 185010034 single base substitution C T upstream_gene_variant ESAD-UK 1 185012856 185012856 single base substitution G C upstream_gene_variant ESAD-UK 1 185013120 185013120 insertion of <=200bp - T upstream_gene_variant ESAD-UK 1 185014537 185014537 single base substitution C A 5_prime_UTR_variant ESAD-UK 1 185014537 185014537 single base substitution C A upstream_gene_variant ESAD-UK 1 185014891 185014891 single base substitution T G intron_variant ESAD-UK 1 185014891 185014891 single base substitution T G upstream_gene_variant ESAD-UK 1 185015403 185015403 single base substitution G A 5_prime_UTR_variant ESAD-UK 1 185015403 185015403 single base substitution G A intron_variant ESAD-UK 1 185017244 185017244 single base substitution G A intron_variant ESAD-UK 1 185019364 185019364 single base substitution C A intron_variant ESAD-UK 1 185019599 185019599 single base substitution C A intron_variant ESAD-UK 1 185020996 185020996 insertion of <=200bp - AT intron_variant ESAD-UK 1 185022883 185022883 single base substitution C T intron_variant ESAD-UK 1 185023823 185023823 single base substitution T A intron_variant ESAD-UK 1 185024275 185024275 single base substitution A C intron_variant ESAD-UK 1 185030504 185030504 single base substitution A G intron_variant ESAD-UK 1 185031952 185031952 single base substitution C A intron_variant ESAD-UK 1 185032070 185032070 single base substitution T A intron_variant ESAD-UK 1 185033106 185033106 single base substitution C T intron_variant ESAD-UK 1 185033726 185033726 single base substitution G T intron_variant ESAD-UK 1 185033829 185033829 single base substitution G C intron_variant ESAD-UK 1 185035704 185035704 single base substitution C G intron_variant ESAD-UK 1 185037149 185037149 single base substitution T G intron_variant ESAD-UK 1 185037386 185037386 single base substitution T G intron_variant ESAD-UK 1 185037501 185037501 single base substitution G T intron_variant ESAD-UK 1 185039594 185039594 single base substitution C T intron_variant ESAD-UK 1 185041391 185041391 deletion of <=200bp T - intron_variant ESAD-UK 1 185042299 185042299 insertion of <=200bp - T intron_variant ESAD-UK 1 185046461 185046461 deletion of <=200bp T - intron_variant ESAD-UK 1 185048706 185048706 single base substitution C A intron_variant ESAD-UK 1 185050026 185050028 deletion of <=200bp AGA - intron_variant ESAD-UK 1 185050095 185050095 single base substitution G A intron_variant ESAD-UK 1 185051175 185051175 single base substitution G A intron_variant ESAD-UK 1 185052024 185052024 single base substitution T C intron_variant ESAD-UK 1 185052411 185052411 single base substitution G A intron_variant ESAD-UK 1 185052944 185052944 single base substitution G T intron_variant ESAD-UK 1 185053692 185053692 single base substitution T C intron_variant ESAD-UK 1 185054656 185054656 single base substitution C T intron_variant ESAD-UK 1 185055229 185055229 single base substitution G A intron_variant ESAD-UK 1 185055286 185055286 single base substitution C G intron_variant ESAD-UK 1 185055493 185055493 deletion of <=200bp T - intron_variant ESAD-UK 1 185057223 185057223 single base substitution G A intron_variant ESAD-UK 1 185057310 185057310 single base substitution T A intron_variant ESAD-UK 1 185057965 185057965 single base substitution T A intron_variant ESAD-UK 1 185061341 185061341 single base substitution C G downstream_gene_variant ESAD-UK 1 185061341 185061341 single base substitution C G intron_variant ESAD-UK 1 185062218 185062218 insertion of <=200bp - A downstream_gene_variant ESAD-UK 1 185062218 185062218 insertion of <=200bp - A frameshift_variant K92K? ESAD-UK 1 185062218 185062218 insertion of <=200bp - A intron_variant ESAD-UK 1 185062376 185062376 single base substitution T C downstream_gene_variant ESAD-UK 1 185062376 185062376 single base substitution T C intron_variant ESAD-UK 1 185062376 185062376 single base substitution T C synonymous_variant I144I 432T>C ESAD-UK 1 185062776 185062776 single base substitution C T downstream_gene_variant ESAD-UK 1 185062776 185062776 single base substitution C T intron_variant ESAD-UK 1 185063842 185063842 single base substitution A T downstream_gene_variant ESAD-UK 1 185063842 185063842 single base substitution A T intron_variant ESAD-UK 1 185068755 185068755 single base substitution A G intron_variant ESAD-UK 1 185069057 185069057 single base substitution A T downstream_gene_variant ESAD-UK 1 185069057 185069057 single base substitution A T missense_variant Y219F 656A>T ESAD-UK 1 185069057 185069057 single base substitution A T missense_variant Y291F 872A>T ESAD-UK 1 185070019 185070019 single base substitution C G 3_prime_UTR_variant ESAD-UK 1 185070019 185070019 single base substitution C G downstream_gene_variant ESAD-UK 1 185070256 185070256 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 1 185070256 185070256 deletion of <=200bp T - downstream_gene_variant ESAD-UK 1 185070571 185070571 single base substitution A C 3_prime_UTR_variant ESAD-UK 1 185070571 185070571 single base substitution A C downstream_gene_variant ESAD-UK 1 185071111 185071111 single base substitution T G 3_prime_UTR_variant ESAD-UK 1 185071111 185071111 single base substitution T G downstream_gene_variant ESAD-UK 1 185072627 185072627 single base substitution G A downstream_gene_variant GBM-US 1 185069006 185069006 single base substitution G A downstream_gene_variant GBM-US 1 185069006 185069006 single base substitution G A missense_variant S202N 605G>A GBM-US 1 185069006 185069006 single base substitution G A missense_variant S274N 821G>A KIRP-US 1 185060812 185060812 single base substitution T C exon_variant KIRP-US 1 185060812 185060812 single base substitution T C synonymous_variant T63T 189T>C LAML-KR 1 185053059 185053059 single base substitution A T intron_variant LAML-KR 1 185063276 185063276 single base substitution A T downstream_gene_variant LAML-KR 1 185063276 185063276 single base substitution A T intron_variant LICA-FR 1 185020728 185020728 single base substitution A G intron_variant LICA-FR 1 185050054 185050054 single base substitution C A intron_variant LIHC-US 1 185067215 185067215 single base substitution G T missense_variant G159V 476G>T LIHC-US 1 185067215 185067215 single base substitution G T missense_variant G87V 260G>T LINC-JP 1 185018803 185018803 deletion of <=200bp A - intron_variant LINC-JP 1 185029367 185029367 insertion of <=200bp - T intron_variant LINC-JP 1 185029901 185029901 single base substitution G A intron_variant LINC-JP 1 185041184 185041184 single base substitution G A intron_variant LINC-JP 1 185055446 185055446 single base substitution T G intron_variant LINC-JP 1 185055732 185055732 single base substitution T G intron_variant LINC-JP 1 185057145 185057145 single base substitution G A intron_variant LINC-JP 1 185058451 185058451 single base substitution C A intron_variant LINC-JP 1 185069687 185069687 single base substitution C T 3_prime_UTR_variant LINC-JP 1 185069687 185069687 single base substitution C T downstream_gene_variant LINC-JP 1 185073865 185073865 single base substitution G A downstream_gene_variant LIRI-JP 1 185010032 185010032 single base substitution C T upstream_gene_variant LIRI-JP 1 185010790 185010790 single base substitution G C upstream_gene_variant LIRI-JP 1 185016729 185016729 single base substitution C G intron_variant LIRI-JP 1 185018303 185018303 single base substitution C A intron_variant LIRI-JP 1 185023808 185023808 single base substitution T C intron_variant LIRI-JP 1 185024076 185024076 single base substitution C A intron_variant LIRI-JP 1 185024204 185024204 single base substitution G A intron_variant LIRI-JP 1 185027115 185027115 single base substitution G A intron_variant LIRI-JP 1 185027260 185027260 single base substitution A G intron_variant LIRI-JP 1 185028524 185028524 single base substitution G T intron_variant LIRI-JP 1 185028915 185028934 deletion of <=200bp AATTATATTTTTATCTCTAG - intron_variant LIRI-JP 1 185029432 185029432 single base substitution A G intron_variant LIRI-JP 1 185033047 185033047 single base substitution T A intron_variant LIRI-JP 1 185033311 185033311 insertion of <=200bp - A intron_variant LIRI-JP 1 185037873 185037873 single base substitution A T intron_variant LIRI-JP 1 185037886 185037886 single base substitution T G intron_variant LIRI-JP 1 185038360 185038360 single base substitution G A intron_variant LIRI-JP 1 185040024 185040024 single base substitution T C intron_variant LIRI-JP 1 185040025 185040025 single base substitution C T intron_variant LIRI-JP 1 185041654 185041654 single base substitution T C intron_variant LIRI-JP 1 185041803 185041803 single base substitution C A intron_variant LIRI-JP 1 185043152 185043152 single base substitution A G intron_variant LIRI-JP 1 185047640 185047640 single base substitution G A intron_variant LIRI-JP 1 185047744 185047744 single base substitution G T intron_variant LIRI-JP 1 185049839 185049839 single base substitution G A intron_variant LIRI-JP 1 185051967 185051967 single base substitution A C intron_variant LIRI-JP 1 185053096 185053096 single base substitution T G intron_variant LIRI-JP 1 185053159 185053159 single base substitution A G intron_variant LIRI-JP 1 185055265 185055265 single base substitution A G intron_variant LIRI-JP 1 185055449 185055449 single base substitution G T intron_variant LIRI-JP 1 185057437 185057437 single base substitution G C intron_variant LIRI-JP 1 185061791 185061791 single base substitution A G downstream_gene_variant LIRI-JP 1 185061791 185061791 single base substitution A G intron_variant LIRI-JP 1 185062474 185062474 deletion of <=200bp A - downstream_gene_variant LIRI-JP 1 185062474 185062474 deletion of <=200bp A - intron_variant LIRI-JP 1 185065398 185065398 single base substitution A G downstream_gene_variant LIRI-JP 1 185065398 185065398 single base substitution A G intron_variant LIRI-JP 1 185068484 185068484 single base substitution T C intron_variant LIRI-JP 1 185068791 185068791 single base substitution T A intron_variant LIRI-JP 1 185071722 185071722 single base substitution T A 3_prime_UTR_variant LIRI-JP 1 185071722 185071722 single base substitution T A downstream_gene_variant LIRI-JP 1 185073083 185073083 single base substitution A G downstream_gene_variant LIRI-JP 1 185073426 185073426 single base substitution C A downstream_gene_variant LIRI-JP 1 185074240 185074240 single base substitution T C downstream_gene_variant LIRI-JP 1 185075809 185075809 single base substitution T C downstream_gene_variant LUSC-KR 1 185013684 185013684 single base substitution A T upstream_gene_variant LUSC-KR 1 185017375 185017375 single base substitution G A intron_variant LUSC-KR 1 185020742 185020742 single base substitution G A intron_variant LUSC-KR 1 185020845 185020845 single base substitution A T intron_variant LUSC-KR 1 185023859 185023859 single base substitution G T intron_variant LUSC-KR 1 185029755 185029755 single base substitution A T intron_variant LUSC-KR 1 185031190 185031190 single base substitution T A intron_variant LUSC-KR 1 185048570 185048570 single base substitution G T intron_variant LUSC-KR 1 185048677 185048677 single base substitution C A intron_variant LUSC-KR 1 185050684 185050684 single base substitution C A intron_variant LUSC-KR 1 185054261 185054261 single base substitution A C intron_variant LUSC-KR 1 185060988 185060988 single base substitution C A exon_variant LUSC-KR 1 185060988 185060988 single base substitution C A intron_variant LUSC-KR 1 185063276 185063276 single base substitution A T downstream_gene_variant LUSC-KR 1 185063276 185063276 single base substitution A T intron_variant LUSC-KR 1 185067474 185067474 single base substitution G T splice_region_variant LUSC-KR 1 185070375 185070375 single base substitution C G 3_prime_UTR_variant LUSC-KR 1 185070375 185070375 single base substitution C G downstream_gene_variant LUSC-KR 1 185072031 185072031 single base substitution G A downstream_gene_variant MALY-DE 1 185014675 185014675 single base substitution A G 5_prime_UTR_variant MALY-DE 1 185014675 185014675 single base substitution A G exon_variant MALY-DE 1 185014675 185014675 single base substitution A G upstream_gene_variant MALY-DE 1 185017899 185017899 deletion of <=200bp A - intron_variant MALY-DE 1 185018803 185018803 deletion of <=200bp A - intron_variant MALY-DE 1 185023828 185023828 single base substitution T A intron_variant MALY-DE 1 185026951 185026951 single base substitution A C intron_variant MALY-DE 1 185030733 185030733 single base substitution A G intron_variant MALY-DE 1 185031952 185031952 single base substitution C A intron_variant MALY-DE 1 185038441 185038441 single base substitution C A intron_variant MALY-DE 1 185041922 185041922 single base substitution A T intron_variant MALY-DE 1 185047086 185047086 single base substitution A G intron_variant MALY-DE 1 185050630 185050630 single base substitution A G intron_variant MALY-DE 1 185052167 185052167 single base substitution C G intron_variant MALY-DE 1 185057464 185057464 single base substitution G C intron_variant MALY-DE 1 185057465 185057465 insertion of <=200bp - AC intron_variant MALY-DE 1 185060002 185060002 single base substitution C G intron_variant MALY-DE 1 185060497 185060497 single base substitution A G intron_variant MALY-DE 1 185065701 185065701 single base substitution T G downstream_gene_variant MALY-DE 1 185065701 185065701 single base substitution T G intron_variant MALY-DE 1 185071196 185071196 single base substitution T C 3_prime_UTR_variant MALY-DE 1 185071196 185071196 single base substitution T C downstream_gene_variant MELA-AU 1 185009602 185009602 single base substitution G A upstream_gene_variant MELA-AU 1 185009606 185009606 single base substitution G T upstream_gene_variant MELA-AU 1 185009696 185009696 single base substitution C T upstream_gene_variant MELA-AU 1 185009720 185009720 single base substitution C T upstream_gene_variant MELA-AU 1 185009826 185009826 single base substitution G T upstream_gene_variant MELA-AU 1 185010108 185010108 single base substitution A G upstream_gene_variant MELA-AU 1 185010650 185010650 single base substitution C T upstream_gene_variant MELA-AU 1 185011105 185011105 single base substitution G T upstream_gene_variant MELA-AU 1 185011655 185011655 single base substitution A C upstream_gene_variant MELA-AU 1 185011830 185011830 single base substitution G A upstream_gene_variant MELA-AU 1 185011874 185011874 single base substitution G A upstream_gene_variant MELA-AU 1 185011960 185011960 single base substitution T A upstream_gene_variant MELA-AU 1 185012221 185012221 single base substitution G A upstream_gene_variant MELA-AU 1 185012531 185012531 single base substitution C A upstream_gene_variant MELA-AU 1 185012727 185012727 single base substitution C T upstream_gene_variant MELA-AU 1 185012850 185012850 single base substitution G A upstream_gene_variant MELA-AU 1 185013375 185013375 single base substitution G A upstream_gene_variant MELA-AU 1 185013490 185013490 single base substitution G A upstream_gene_variant MELA-AU 1 185013659 185013659 single base substitution G A upstream_gene_variant MELA-AU 1 185014371 185014371 single base substitution G A upstream_gene_variant MELA-AU 1 185014391 185014391 single base substitution C T upstream_gene_variant MELA-AU 1 185017292 185017292 single base substitution C T intron_variant MELA-AU 1 185017348 185017348 single base substitution G A intron_variant MELA-AU 1 185017911 185017911 single base substitution C T intron_variant MELA-AU 1 185018068 185018068 single base substitution G T intron_variant MELA-AU 1 185018147 185018147 single base substitution C T intron_variant MELA-AU 1 185018295 185018295 single base substitution T C intron_variant MELA-AU 1 185018662 185018662 single base substitution C T intron_variant MELA-AU 1 185018944 185018944 single base substitution T G intron_variant MELA-AU 1 185019155 185019155 single base substitution C T intron_variant MELA-AU 1 185019762 185019762 single base substitution T G intron_variant MELA-AU 1 185019791 185019791 single base substitution C T intron_variant MELA-AU 1 185020053 185020053 single base substitution C T intron_variant MELA-AU 1 185020212 185020212 single base substitution C T intron_variant MELA-AU 1 185020686 185020686 single base substitution C T intron_variant MELA-AU 1 185020695 185020695 single base substitution C T intron_variant MELA-AU 1 185021821 185021821 single base substitution C T intron_variant MELA-AU 1 185022351 185022351 single base substitution C T intron_variant MELA-AU 1 185022651 185022651 single base substitution C T intron_variant MELA-AU 1 185022730 185022730 single base substitution C T intron_variant MELA-AU 1 185023449 185023449 single base substitution C T intron_variant MELA-AU 1 185023675 185023675 single base substitution C T intron_variant MELA-AU 1 185023719 185023719 single base substitution C T intron_variant MELA-AU 1 185024378 185024378 single base substitution G A intron_variant MELA-AU 1 185024419 185024419 single base substitution G A intron_variant MELA-AU 1 185024778 185024778 single base substitution C T intron_variant MELA-AU 1 185026439 185026439 single base substitution T A intron_variant MELA-AU 1 185026444 185026444 single base substitution A G intron_variant MELA-AU 1 185027144 185027144 single base substitution T C intron_variant MELA-AU 1 185027436 185027436 single base substitution T C intron_variant MELA-AU 1 185027755 185027755 single base substitution G A intron_variant MELA-AU 1 185028304 185028304 single base substitution G A intron_variant MELA-AU 1 185028945 185028945 single base substitution C T intron_variant MELA-AU 1 185029411 185029411 single base substitution C G intron_variant MELA-AU 1 185029830 185029830 single base substitution C T intron_variant MELA-AU 1 185030457 185030457 single base substitution C T intron_variant MELA-AU 1 185031661 185031661 single base substitution C T intron_variant MELA-AU 1 185032167 185032167 single base substitution C T intron_variant MELA-AU 1 185034999 185034999 deletion of <=200bp T - intron_variant MELA-AU 1 185035007 185035007 single base substitution C T intron_variant MELA-AU 1 185036743 185036743 single base substitution T C intron_variant MELA-AU 1 185037432 185037433 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 185037497 185037497 single base substitution C T intron_variant MELA-AU 1 185038583 185038583 single base substitution C T intron_variant MELA-AU 1 185038705 185038705 single base substitution T G intron_variant MELA-AU 1 185038754 185038754 single base substitution T G intron_variant MELA-AU 1 185039809 185039809 single base substitution C T intron_variant MELA-AU 1 185039844 185039844 single base substitution C T intron_variant MELA-AU 1 185040057 185040057 single base substitution C T intron_variant MELA-AU 1 185041633 185041633 single base substitution T C intron_variant MELA-AU 1 185042386 185042386 single base substitution C T intron_variant MELA-AU 1 185042424 185042424 single base substitution T A intron_variant MELA-AU 1 185042487 185042487 single base substitution C T intron_variant MELA-AU 1 185043080 185043080 single base substitution C A intron_variant MELA-AU 1 185043517 185043517 single base substitution T C intron_variant MELA-AU 1 185043560 185043560 single base substitution C T intron_variant MELA-AU 1 185043561 185043561 single base substitution C T intron_variant MELA-AU 1 185043584 185043584 single base substitution C T intron_variant MELA-AU 1 185044042 185044043 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 1 185044081 185044081 single base substitution C T intron_variant MELA-AU 1 185044920 185044920 single base substitution C T intron_variant MELA-AU 1 185045453 185045453 single base substitution C T intron_variant MELA-AU 1 185046582 185046583 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 185047060 185047060 single base substitution A G intron_variant MELA-AU 1 185047065 185047065 single base substitution C T intron_variant MELA-AU 1 185047143 185047143 single base substitution C T intron_variant MELA-AU 1 185047250 185047250 single base substitution G T intron_variant MELA-AU 1 185047576 185047576 single base substitution G T intron_variant MELA-AU 1 185047912 185047912 single base substitution C T intron_variant MELA-AU 1 185048100 185048100 single base substitution C T intron_variant MELA-AU 1 185048131 185048131 single base substitution C T intron_variant MELA-AU 1 185048691 185048691 single base substitution A G intron_variant MELA-AU 1 185049212 185049212 single base substitution C T intron_variant MELA-AU 1 185049243 185049243 single base substitution C T intron_variant MELA-AU 1 185050373 185050373 single base substitution C T intron_variant MELA-AU 1 185050489 185050489 single base substitution T C intron_variant MELA-AU 1 185051273 185051273 single base substitution G A intron_variant MELA-AU 1 185051573 185051573 single base substitution C T intron_variant MELA-AU 1 185051986 185052001 deletion of <=200bp AAGTCGTTAGCAAAAA - intron_variant MELA-AU 1 185052410 185052410 single base substitution C T intron_variant MELA-AU 1 185053886 185053886 single base substitution A C intron_variant MELA-AU 1 185053949 185053949 single base substitution G A intron_variant MELA-AU 1 185054118 185054118 single base substitution C T intron_variant MELA-AU 1 185054525 185054525 single base substitution C T intron_variant MELA-AU 1 185054617 185054617 single base substitution C T intron_variant MELA-AU 1 185054816 185054816 single base substitution C T intron_variant MELA-AU 1 185055003 185055003 single base substitution C T intron_variant MELA-AU 1 185055210 185055210 single base substitution C T intron_variant MELA-AU 1 185055239 185055239 single base substitution T A intron_variant MELA-AU 1 185055258 185055258 single base substitution C T intron_variant MELA-AU 1 185055519 185055519 single base substitution C T intron_variant MELA-AU 1 185057035 185057035 single base substitution A G intron_variant MELA-AU 1 185057515 185057515 single base substitution C T intron_variant MELA-AU 1 185057682 185057682 single base substitution C T intron_variant MELA-AU 1 185057895 185057895 single base substitution C T intron_variant MELA-AU 1 185058574 185058574 single base substitution C T intron_variant MELA-AU 1 185058691 185058691 single base substitution T C intron_variant MELA-AU 1 185059060 185059060 single base substitution G A intron_variant MELA-AU 1 185059072 185059072 single base substitution G A intron_variant MELA-AU 1 185059074 185059074 single base substitution G A intron_variant MELA-AU 1 185059436 185059436 single base substitution C T intron_variant MELA-AU 1 185059531 185059531 single base substitution C T intron_variant MELA-AU 1 185059564 185059564 single base substitution C T intron_variant MELA-AU 1 185060155 185060155 single base substitution C T intron_variant MELA-AU 1 185060634 185060634 single base substitution C T intron_variant MELA-AU 1 185061468 185061468 single base substitution C T downstream_gene_variant MELA-AU 1 185061468 185061468 single base substitution C T intron_variant MELA-AU 1 185062087 185062087 single base substitution A G downstream_gene_variant MELA-AU 1 185062087 185062087 single base substitution A G intron_variant MELA-AU 1 185062182 185062182 single base substitution C T downstream_gene_variant MELA-AU 1 185062182 185062182 single base substitution C T intron_variant MELA-AU 1 185062648 185062648 single base substitution C T downstream_gene_variant MELA-AU 1 185062648 185062648 single base substitution C T intron_variant MELA-AU 1 185063460 185063460 single base substitution G C downstream_gene_variant MELA-AU 1 185063460 185063460 single base substitution G C intron_variant MELA-AU 1 185063595 185063595 single base substitution T A downstream_gene_variant MELA-AU 1 185063595 185063595 single base substitution T A intron_variant MELA-AU 1 185063809 185063809 single base substitution C T downstream_gene_variant MELA-AU 1 185063809 185063809 single base substitution C T intron_variant MELA-AU 1 185063944 185063944 single base substitution C T downstream_gene_variant MELA-AU 1 185063944 185063944 single base substitution C T intron_variant MELA-AU 1 185063991 185063991 single base substitution G C downstream_gene_variant MELA-AU 1 185063991 185063991 single base substitution G C intron_variant MELA-AU 1 185064211 185064211 single base substitution A T downstream_gene_variant MELA-AU 1 185064211 185064211 single base substitution A T intron_variant MELA-AU 1 185064569 185064569 single base substitution C T downstream_gene_variant MELA-AU 1 185064569 185064569 single base substitution C T intron_variant MELA-AU 1 185064621 185064621 single base substitution C T downstream_gene_variant MELA-AU 1 185064621 185064621 single base substitution C T intron_variant MELA-AU 1 185065522 185065522 single base substitution C G downstream_gene_variant MELA-AU 1 185065522 185065522 single base substitution C G intron_variant MELA-AU 1 185065625 185065625 single base substitution T A downstream_gene_variant MELA-AU 1 185065625 185065625 single base substitution T A intron_variant MELA-AU 1 185065891 185065891 single base substitution G A downstream_gene_variant MELA-AU 1 185065891 185065891 single base substitution G A intron_variant MELA-AU 1 185067192 185067192 single base substitution C T intron_variant MELA-AU 1 185067250 185067250 single base substitution G A missense_variant E171K 511G>A MELA-AU 1 185067250 185067250 single base substitution G A missense_variant E99K 295G>A MELA-AU 1 185067324 185067324 single base substitution A T missense_variant K123N 369A>T MELA-AU 1 185067324 185067324 single base substitution A T missense_variant K195N 585A>T MELA-AU 1 185068274 185068274 single base substitution C A intron_variant MELA-AU 1 185069848 185069848 single base substitution C T 3_prime_UTR_variant MELA-AU 1 185069848 185069848 single base substitution C T downstream_gene_variant MELA-AU 1 185069907 185069907 single base substitution C T 3_prime_UTR_variant MELA-AU 1 185069907 185069907 single base substitution C T downstream_gene_variant MELA-AU 1 185070032 185070032 single base substitution A T 3_prime_UTR_variant MELA-AU 1 185070032 185070032 single base substitution A T downstream_gene_variant MELA-AU 1 185070057 185070057 single base substitution C T 3_prime_UTR_variant MELA-AU 1 185070057 185070057 single base substitution C T downstream_gene_variant MELA-AU 1 185072162 185072162 single base substitution T G downstream_gene_variant MELA-AU 1 185074137 185074137 insertion of <=200bp - T downstream_gene_variant MELA-AU 1 185075467 185075467 single base substitution C T downstream_gene_variant MELA-AU 1 185075669 185075669 single base substitution C T downstream_gene_variant MELA-AU 1 185076072 185076072 single base substitution C T downstream_gene_variant MELA-AU 1 185076136 185076136 single base substitution C T downstream_gene_variant ORCA-IN 1 185010531 185010531 single base substitution C G upstream_gene_variant ORCA-IN 1 185026530 185026530 single base substitution G C intron_variant ORCA-IN 1 185028984 185028984 single base substitution G C intron_variant ORCA-IN 1 185029422 185029422 single base substitution C T intron_variant ORCA-IN 1 185040003 185040003 single base substitution C T intron_variant ORCA-IN 1 185047817 185047817 single base substitution G A intron_variant ORCA-IN 1 185049075 185049075 deletion of <=200bp G - intron_variant ORCA-IN 1 185061763 185061763 single base substitution C T downstream_gene_variant ORCA-IN 1 185061763 185061763 single base substitution C T intron_variant OV-AU 1 185009770 185009770 single base substitution C T upstream_gene_variant OV-AU 1 185012915 185012915 single base substitution G T upstream_gene_variant OV-AU 1 185017977 185017977 single base substitution G C intron_variant OV-AU 1 185018643 185018643 single base substitution C A intron_variant OV-AU 1 185021367 185021367 single base substitution C G intron_variant OV-AU 1 185022018 185022018 single base substitution A G intron_variant OV-AU 1 185025781 185025781 single base substitution G C intron_variant OV-AU 1 185031040 185031040 single base substitution G C intron_variant OV-AU 1 185033971 185033971 single base substitution G A intron_variant OV-AU 1 185035596 185035596 single base substitution C G intron_variant OV-AU 1 185037426 185037426 single base substitution A T intron_variant OV-AU 1 185038801 185038801 single base substitution A T intron_variant OV-AU 1 185054163 185054163 single base substitution C G intron_variant OV-AU 1 185054808 185054808 single base substitution C G intron_variant OV-AU 1 185056686 185056686 single base substitution A G splice_region_variant OV-AU 1 185056686 185056686 single base substitution A G start_lost M1V 1A>G OV-AU 1 185073388 185073388 single base substitution A G downstream_gene_variant OV-AU 1 185074885 185074885 single base substitution T A downstream_gene_variant OV-AU 1 185076087 185076087 single base substitution T G downstream_gene_variant PACA-AU 1 185010435 185010435 single base substitution G T upstream_gene_variant PACA-AU 1 185021072 185021072 single base substitution A C intron_variant PACA-AU 1 185023823 185023823 single base substitution T A intron_variant PACA-AU 1 185026934 185026934 deletion of <=200bp G - intron_variant PACA-AU 1 185028321 185028321 deletion of <=200bp A - intron_variant PACA-AU 1 185032071 185032071 single base substitution A T intron_variant PACA-AU 1 185034142 185034142 single base substitution G A intron_variant PACA-AU 1 185039937 185039937 deletion of <=200bp T - intron_variant PACA-AU 1 185042145 185042145 single base substitution T A intron_variant PACA-AU 1 185045211 185045211 single base substitution A C intron_variant PACA-AU 1 185045824 185045824 single base substitution C A intron_variant PACA-AU 1 185045852 185045852 single base substitution C T intron_variant PACA-AU 1 185046109 185046109 single base substitution C T intron_variant PACA-AU 1 185046366 185046366 single base substitution C A intron_variant PACA-AU 1 185046550 185046550 single base substitution C G intron_variant PACA-AU 1 185047010 185047010 single base substitution C G intron_variant PACA-AU 1 185051174 185051174 single base substitution C T intron_variant PACA-AU 1 185052795 185052795 single base substitution G A intron_variant PACA-AU 1 185052914 185052914 insertion of <=200bp - T intron_variant PACA-AU 1 185053429 185053429 single base substitution C T intron_variant PACA-AU 1 185055479 185055479 single base substitution C T intron_variant PACA-AU 1 185056246 185056246 single base substitution C G intron_variant PACA-AU 1 185056450 185056450 single base substitution C G intron_variant PACA-AU 1 185056500 185056500 single base substitution G A intron_variant PACA-AU 1 185061514 185061514 single base substitution G C downstream_gene_variant PACA-AU 1 185061514 185061514 single base substitution G C intron_variant PACA-AU 1 185062294 185062294 single base substitution G A downstream_gene_variant PACA-AU 1 185062294 185062294 single base substitution G A intron_variant PACA-AU 1 185062294 185062294 single base substitution G A missense_variant R117H 350G>A PACA-AU 1 185064451 185064451 single base substitution C T downstream_gene_variant PACA-AU 1 185064451 185064451 single base substitution C T intron_variant PACA-AU 1 185066688 185066688 single base substitution G C intron_variant PACA-CA 1 185025042 185025042 deletion of <=200bp T - intron_variant PACA-CA 1 185025249 185025249 single base substitution A T intron_variant PACA-CA 1 185028797 185028797 single base substitution A T intron_variant PACA-CA 1 185030640 185030640 single base substitution G T intron_variant PACA-CA 1 185031952 185031952 single base substitution C A intron_variant PACA-CA 1 185032127 185032127 single base substitution C T intron_variant PACA-CA 1 185034545 185034545 single base substitution G C intron_variant PACA-CA 1 185037431 185037431 deletion of <=200bp C - intron_variant PACA-CA 1 185043349 185043349 single base substitution C T intron_variant PACA-CA 1 185052714 185052714 single base substitution G A intron_variant PACA-CA 1 185056432 185056432 single base substitution A G intron_variant PACA-CA 1 185058728 185058728 single base substitution T A intron_variant PACA-CA 1 185058791 185058791 single base substitution C G intron_variant PACA-CA 1 185061536 185061536 single base substitution T G downstream_gene_variant PACA-CA 1 185061536 185061536 single base substitution T G intron_variant PACA-CA 1 185064240 185064240 single base substitution C G downstream_gene_variant PACA-CA 1 185064240 185064240 single base substitution C G intron_variant PACA-CA 1 185064303 185064303 single base substitution G A downstream_gene_variant PACA-CA 1 185064303 185064303 single base substitution G A intron_variant PACA-CA 1 185066135 185066135 single base substitution T C downstream_gene_variant PACA-CA 1 185066135 185066135 single base substitution T C intron_variant PACA-CA 1 185069602 185069602 single base substitution C G 3_prime_UTR_variant PACA-CA 1 185069602 185069602 single base substitution C G downstream_gene_variant PACA-CA 1 185072438 185072438 single base substitution A T downstream_gene_variant PACA-CA 1 185072599 185072599 single base substitution A G downstream_gene_variant PACA-CA 1 185073865 185073865 single base substitution G A downstream_gene_variant PACA-CA 1 185074202 185074202 single base substitution A T downstream_gene_variant PACA-CA 1 185075151 185075151 single base substitution A T downstream_gene_variant PACA-CA 1 185075956 185075956 single base substitution A C downstream_gene_variant PAEN-AU 1 185041859 185041859 single base substitution T G intron_variant PBCA-DE 1 185019275 185019275 single base substitution G A intron_variant PBCA-DE 1 185022644 185022644 deletion of <=200bp T - intron_variant PBCA-DE 1 185027497 185027497 single base substitution A C intron_variant PBCA-DE 1 185031951 185031951 single base substitution C A intron_variant PBCA-DE 1 185039694 185039694 single base substitution T C intron_variant PBCA-DE 1 185045385 185045385 deletion of <=200bp G - intron_variant PBCA-DE 1 185045812 185045812 insertion of <=200bp - T intron_variant PBCA-DE 1 185054825 185054825 single base substitution G A intron_variant PBCA-DE 1 185060674 185060674 deletion of <=200bp T - intron_variant PBCA-DE 1 185066236 185066236 single base substitution C A intron_variant PBCA-DE 1 185075607 185075607 insertion of <=200bp - A downstream_gene_variant PRAD-CA 1 185016143 185016143 single base substitution T A intron_variant PRAD-CA 1 185026527 185026527 single base substitution G C intron_variant PRAD-CA 1 185030504 185030504 single base substitution A G intron_variant PRAD-CA 1 185036017 185036017 single base substitution A G intron_variant PRAD-CA 1 185040987 185040987 single base substitution T C intron_variant PRAD-CA 1 185055592 185055592 single base substitution A G intron_variant PRAD-CA 1 185071995 185071995 single base substitution T C downstream_gene_variant PRAD-UK 1 185014354 185014354 single base substitution A G upstream_gene_variant PRAD-UK 1 185020821 185020821 single base substitution C A intron_variant PRAD-UK 1 185021840 185021840 single base substitution A T intron_variant PRAD-UK 1 185026522 185026522 deletion of <=200bp T - intron_variant PRAD-UK 1 185026527 185026527 single base substitution G C intron_variant PRAD-UK 1 185041033 185041033 single base substitution C G intron_variant PRAD-UK 1 185060234 185060234 single base substitution A C intron_variant PRAD-UK 1 185071640 185071640 single base substitution G T 3_prime_UTR_variant PRAD-UK 1 185071640 185071640 single base substitution G T downstream_gene_variant PRAD-UK 1 185076595 185076595 single base substitution A G downstream_gene_variant READ-US 1 185056762 185056762 single base substitution G A exon_variant READ-US 1 185056762 185056762 single base substitution G A missense_variant R26Q 77G>A READ-US 1 185069003 185069003 single base substitution G A downstream_gene_variant READ-US 1 185069003 185069003 single base substitution G A missense_variant R201Q 602G>A READ-US 1 185069003 185069003 single base substitution G A missense_variant R273Q 818G>A RECA-EU 1 185012312 185012312 single base substitution G C upstream_gene_variant RECA-EU 1 185032049 185032049 single base substitution A G intron_variant RECA-EU 1 185035619 185035619 single base substitution A T intron_variant RECA-EU 1 185036391 185036391 single base substitution C T intron_variant RECA-EU 1 185037757 185037757 single base substitution C T intron_variant RECA-EU 1 185051037 185051037 single base substitution C T intron_variant RECA-EU 1 185055444 185055444 single base substitution A G intron_variant SKCA-BR 1 185010580 185010580 single base substitution G C upstream_gene_variant SKCA-BR 1 185011225 185011225 single base substitution G A upstream_gene_variant SKCA-BR 1 185014461 185014461 single base substitution G A upstream_gene_variant SKCA-BR 1 185015134 185015134 single base substitution C G intron_variant SKCA-BR 1 185015134 185015134 single base substitution C G upstream_gene_variant SKCA-BR 1 185015140 185015140 single base substitution C G intron_variant SKCA-BR 1 185015140 185015140 single base substitution C G upstream_gene_variant SKCA-BR 1 185024813 185024813 single base substitution G A intron_variant SKCA-BR 1 185025733 185025733 single base substitution C G intron_variant SKCA-BR 1 185025740 185025740 single base substitution T G intron_variant SKCA-BR 1 185025747 185025747 single base substitution C T intron_variant SKCA-BR 1 185026813 185026813 single base substitution A G intron_variant SKCA-BR 1 185027610 185027610 single base substitution C T intron_variant SKCA-BR 1 185030260 185030261 deletion of <=200bp CT - intron_variant SKCA-BR 1 185030385 185030385 single base substitution G A intron_variant SKCA-BR 1 185036840 185036841 deletion of <=200bp CT - intron_variant SKCA-BR 1 185038989 185038989 single base substitution T C intron_variant SKCA-BR 1 185040681 185040681 single base substitution A T intron_variant SKCA-BR 1 185040753 185040753 single base substitution A C intron_variant SKCA-BR 1 185041182 185041182 single base substitution G A intron_variant SKCA-BR 1 185042191 185042192 deletion of <=200bp CT - intron_variant SKCA-BR 1 185048211 185048211 insertion of <=200bp - CTT intron_variant SKCA-BR 1 185055672 185055672 single base substitution G A intron_variant SKCA-BR 1 185061183 185061183 single base substitution A C downstream_gene_variant SKCA-BR 1 185061183 185061183 single base substitution A C intron_variant SKCA-BR 1 185061494 185061494 single base substitution A G downstream_gene_variant SKCA-BR 1 185061494 185061494 single base substitution A G intron_variant SKCA-BR 1 185061698 185061698 single base substitution C T downstream_gene_variant SKCA-BR 1 185061698 185061698 single base substitution C T intron_variant SKCA-BR 1 185067191 185067191 single base substitution C T intron_variant SKCA-BR 1 185068183 185068183 insertion of <=200bp - CT intron_variant SKCA-BR 1 185069445 185069445 single base substitution C T 3_prime_UTR_variant SKCA-BR 1 185069445 185069445 single base substitution C T downstream_gene_variant SKCA-BR 1 185069545 185069545 single base substitution C T 3_prime_UTR_variant SKCA-BR 1 185069545 185069545 single base substitution C T downstream_gene_variant SKCA-BR 1 185069776 185069776 single base substitution C T 3_prime_UTR_variant SKCA-BR 1 185069776 185069776 single base substitution C T downstream_gene_variant SKCA-BR 1 185070034 185070034 insertion of <=200bp - GT 3_prime_UTR_variant SKCA-BR 1 185070034 185070034 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 1 185070057 185070057 single base substitution C T 3_prime_UTR_variant SKCA-BR 1 185070057 185070057 single base substitution C T downstream_gene_variant SKCA-BR 1 185070542 185070542 single base substitution C G 3_prime_UTR_variant SKCA-BR 1 185070542 185070542 single base substitution C G downstream_gene_variant SKCA-BR 1 185070964 185070965 deletion of <=200bp GT - 3_prime_UTR_variant SKCA-BR 1 185070964 185070965 deletion of <=200bp GT - downstream_gene_variant SKCA-BR 1 185074355 185074355 single base substitution A G downstream_gene_variant SKCA-BR 1 185076326 185076326 single base substitution C T downstream_gene_variant SKCM-US 1 185056719 185056719 single base substitution C T exon_variant SKCM-US 1 185056719 185056719 single base substitution C T missense_variant P12S 34C>T SKCM-US 1 185062302 185062302 single base substitution T C downstream_gene_variant SKCM-US 1 185062302 185062302 single base substitution T C intron_variant SKCM-US 1 185062302 185062302 single base substitution T C missense_variant Y120H 358T>C STAD-US 1 185056762 185056762 single base substitution G A exon_variant STAD-US 1 185056762 185056762 single base substitution G A missense_variant R26Q 77G>A STAD-US 1 185068944 185068944 single base substitution C T downstream_gene_variant STAD-US 1 185068944 185068944 single base substitution C T synonymous_variant N181N 543C>T STAD-US 1 185068944 185068944 single base substitution C T synonymous_variant N253N 759C>T THCA-US 1 185060797 185060797 single base substitution G C exon_variant THCA-US 1 185060797 185060797 single base substitution G C missense_variant L58F 174G>C UCEC-US 1 185056767 185056767 single base substitution C T exon_variant UCEC-US 1 185056767 185056767 single base substitution C T missense_variant P28S 82C>T UCEC-US 1 185060871 185060871 single base substitution G A exon_variant UCEC-US 1 185060871 185060871 single base substitution G A missense_variant G83D 248G>A UCEC-US 1 185060871 185060871 single base substitution G A missense_variant G83E 248G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 260211 COSM3725538 c.591C>T p.T197T Substitution - coding silent 1:185098198-185098198 + T276 COSM4722077 c.988G>A p.A330T Substitution - Missense 1:185100278-185100278 + TCGA-BR-4253-01 COSM2098088 c.759C>T p.N253N Substitution - coding silent 1:185099812-185099812 + Pat_59_B COSM5844800 c.685G>A p.V229I Substitution - Missense 1:185098292-185098292 + ESO-859 COSM1240077 c.900C>T p.G300G Substitution - coding silent 1:185099953-185099953 + 8016470 COSM3385528 c.350G>A p.R117H Substitution - Missense 1:185093162-185093162 + YUSCO COSM1689409 c.344C>T p.P115L Substitution - Missense 1:185093156-185093156 + 107051 COSM95197 c.320A>G p.D107G Substitution - Missense 1:185093132-185093132 + ME011T COSM224181 c.100G>A p.D34N Substitution - Missense 1:185091591-185091591 + ccRCC-33 COSM1663940 c.305C>T p.P102L Substitution - Missense 1:185093117-185093117 + TCGA-DW-7963-01 COSM3984546 c.189T>C p.T63T Substitution - coding silent 1:185091680-185091680 + CHOL07 COSM1744280 c.818G>A p.R273Q Substitution - Missense 1:185099871-185099871 + TCGA-BW-A5NP-01 COSM4942622 c.476G>T p.G159V Substitution - Missense 1:185098083-185098083 + TCGA-EI-6917-01 COSM1744280 c.818G>A p.R273Q Substitution - Missense 1:185099871-185099871 + PD4127a COSM164060 c.375G>C p.E125D Substitution - Missense 1:185093187-185093187 + NB-0433 COSM1287660 c.183C>T p.T61T Substitution - coding silent 1:185091674-185091674 + T1182 COSM4722076 c.472C>T p.R158* Substitution - Nonsense 1:185098079-185098079 + LN18 COSM2098079 c.355G>C p.E119Q Substitution - Missense 1:185093167-185093167 + TCGA-EE-A29M-06 COSM3480144 c.34C>T p.P12S Substitution - Missense 1:185087587-185087587 + SA222 COSM212498 c.258A>C p.E86D Substitution - Missense 1:185093070-185093070 + ccRCC-9 COSM1663939 c.272G>A p.R91Q Substitution - Missense 1:185093084-185093084 + S02342 COSM5692332 c.302G>T p.R101M Substitution - Missense 1:185093114-185093114 + TCGA-06-5411-01 COSM3400093 c.821G>A p.S274N Substitution - Missense 1:185099874-185099874 + ESCC_10 COSM5623749 c.103G>T p.G35C Substitution - Missense 1:185091594-185091594 + 587332 COSM1223953 c.856G>A p.A286T Substitution - Missense 1:185099909-185099909 + TCGA-BT-A2LB-01 COSM3789220 c.50G>A p.W17* Substitution - Nonsense 1:185087603-185087603 + S01453 COSM314850 c.136C>G p.H46D Substitution - Missense 1:185091627-185091627 + TCGA-A2-A0SW-01 COSM424789 c.133C>T p.L45L Substitution - coding silent 1:185091624-185091624 + cSCCP5 COSM137793 c.242G>A p.R81K Substitution - Missense 1:185091733-185091733 + TCGA-BS-A0UL-01 COSM900899 c.11C>T p.A4V Substitution - Missense 1:185087564-185087564 + T3118 COSM1240077 c.900C>T p.G300G Substitution - coding silent 1:185099953-185099953 + UMC11 COSM2098085 c.671G>T p.S224I Substitution - Missense 1:185098278-185098278 + TCGA-AN-A046-01 COSM3803164 c.293G>T p.R98I Substitution - Missense 1:185093105-185093105 + LP6007600 COSM4411650 c.872A>T p.Y291F Substitution - Missense 1:185099925-185099925 + S01453 COSM314850 c.136C>G p.H46D Substitution - Missense 1:185091627-185091627 + TCGA-AN-A046-01 COSM1223954 c.128G>A p.R43Q Substitution - Missense 1:185091619-185091619 + STC263 COSM5052871 c.240T>C p.L80L Substitution - coding silent 1:185091731-185091731 + TCGA-EI-6917-01 COSM167143 c.77G>A p.R26Q Substitution - Missense 1:185087630-185087630 + TCGA-AG-A002-01 COSM263373 c.817C>T p.R273* Substitution - Nonsense 1:185099870-185099870 + TCGA-AP-A051-01 COSM900900 c.82C>T p.P28S Substitution - Missense 1:185087635-185087635 + AOCS-060-1-5 COSM3943203 c.1A>G p.M1V Substitution - Missense 1:185087554-185087554 + MOLT-4 COSM1668273 c.760G>A p.A254T Substitution - Missense 1:185099813-185099813 + XHDG08 COSM4768496 c.746A>C p.K249T Substitution - Missense 1:185099799-185099799 + sysucc-311T COSM167143 c.77G>A p.R26Q Substitution - Missense 1:185087630-185087630 + TCGA-AA-3492-01 COSM1337079 c.924delT p.S310fs*12 Deletion - Frameshift 1:185100214-185100214 + T3670 COSM4722075 c.381A>G p.V127V Substitution - coding silent 1:185093193-185093193 + T2621 COSM167143 c.77G>A p.R26Q Substitution - Missense 1:185087630-185087630 + TCGA-CM-6674-01 COSM1337078 c.587G>A p.R196Q Substitution - Missense 1:185098194-185098194 + SW48 COSM2098073 c.210delT p.C72fs*23 Deletion - Frameshift 1:185091701-185091701 + TCGA-AC-A23H-01 COSM3803165 c.473G>A p.R158Q Substitution - Missense 1:185098080-185098080 + 587376 COSM1223954 c.128G>A p.R43Q Substitution - Missense 1:185091619-185091619 + TCGA-D3-A1Q1-06 COSM3480146 c.358T>C p.Y120H Substitution - Missense 1:185093170-185093170 + BD10T COSM5514486 c.951A>G p.K317K Substitution - coding silent 1:185100241-185100241 + E9 COSM1666343 c.926T>G p.F309C Substitution - Missense 1:185100216-185100216 + TCGA-AX-A060-01 COSM900901 c.248G>A p.G83D Substitution - Missense 1:185091739-185091739 + TCGA-HR-A2OG-01 COSM3480145 c.343C>T p.P115S Substitution - Missense 1:185093155-185093155 + TCGA-ET-A2MY-01 COSM3369465 c.174G>C p.L58F Substitution - Missense 1:185091665-185091665 + TCGA-BR-8680-01 COSM167143 c.77G>A p.R26Q Substitution - Missense 1:185087630-185087630 + DU-145 COSM1668272 c.224G>T p.C75F Substitution - Missense 1:185091715-185091715 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.106674 3p21.31-p21.2 603089 Hs.591490 1q25.3 608985

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer ACCTGCGATGAGGAAAGGAAAGCAG - SpliceAcceptorDeletion . c.68-23_69delCTGCTTTCCTTTCCTCATCGCAGGT 3 52443623 RCCC A C Missense p.F170C c.509T>G 3 52441261 RCCC A C Missense p.F170V c.508T>G 3 52441262 RCCC A C Missense p.W196G c.586T>G 3 52440918 HC A C SpliceDonorSNV . c.67+2T>G 3 52443728 RCCC A C Synonymous p.G312G c.936T>G 3 52439306 RCCC A - Frameshift p.D74Efs*4 c.222delT 3 52442523 RCCC - A Frameshift p.R264Kfs*20 c.788dupT 3 52439924 HC A G Missense p.I643T c.1928T>C 3 52436850 CM A G Missense p.I76T c.227T>C 3 52442518 GBM A G Missense p.L17P c.50T>C 3 52443747 RCCC A G Missense p.V409A c.1226T>C 3 52438493 UCEC A G SpliceDonorSNV . c.122+2T>C 3 52443568 RCCC AG TA Missense p.L622M c.1863_1864delinsTA 3 52437180 LUAD A T Missense p.I662N c.1985T>A 3 52436689 RCCC A T SpliceDonorSNV . c.122+2T>A 3 52443568 RCCC C A Missense p.G109V c.326G>T 3 52442023 RCCC C A Missense p.G4C c.10G>T 3 52443885 STAD C A Missense p.K419N c.1257G>T 3 52437904 PRAD C A Missense p.R417M c.1250G>T 3 52438469 CM C A Nonsense p.E136* c.406G>T 3 52441446 LUAD C A Nonsense p.E402* c.1204G>T 3 52438515 RCCC C A Nonsense p.G128* c.382G>T 3 52441470 RCCC C A SpliceAcceptorSNV . c.932-1G>T 3 52439311 RCCC C A Synonymous p.L17L c.51G>T 3 52443746 LUSC C - Frameshift p.E198Rfs*33 c.592delG 3 52440912 STAD C - Frameshift p.E221Sfs*10 c.661delG 3 52440391 CM C - Frameshift p.R700Gfs*163 c.2097delG 3 52436397 RCCC C G Missense p.D225H c.673G>C 3 52440379 BLCA C G Missense p.D663H c.1987G>C 3 52436687 BLCA C G Missense p.K656N c.1968G>C 3 52436810 BLCA C G Missense p.S10T c.29G>C 3 52443866 RCCC C G Missense p.S123T c.368G>C 3 52441981 ESCA C G SpliceDonorSNV . c.67+1G>C 3 52443729 RCCC C T Missense p.A138T c.412G>A 3 52441440 HNSC C T Missense p.D225N c.673G>A 3 52440379 BRCA C T Missense p.E200K c.598G>A 3 52440906 BRCA C T Missense p.E30K c.88G>A 3 52443604 CM C T Missense p.E54K c.160G>A 3 52442585 RCCC C T Missense p.G340S c.1018G>A 3 52439224 LUAD C T Missense p.G619D c.1856G>A 3 52437188 UCEC C T Missense p.M1I c.3G>A 3 52443892 RCCC C T Missense p.R227H c.680G>A 3 52440372 LUSC C T Missense p.R700Q c.2099G>A 3 52436395 UCEC C T Missense p.V604M c.1810G>A 3 52437234 STAD C T SpliceDonorSNV . c.67+1G>A 3 52443729 RCCC G A IntronicSNV . c.67+8C>T 3 52443722 CM G A Missense p.L416F c.1246C>T 3 52438473 CM G A Missense p.P338S c.1012C>T 3 52439230 BLCA G A Missense p.R179W c.535C>T 3 52441235 LUAD G A Missense p.R227C c.679C>T 3 52440373 OV G A Missense p.R237C c.709C>T 3 52440343 ESCA G A Missense p.T495M c.1484C>T 3 52437677 UCEC G A Nonsense p.Q156* c.466C>T 3 52441304 RCCC G A Nonsense p.Q253* c.757C>T 3 52440295 RCCC G A Nonsense p.Q267* c.799C>T 3 52439913 RCCC G A Nonsense p.Q280* c.838C>T 3 52439874 BRCA G A Nonsense p.Q40* c.118C>T 3 52443574 RCCC G A Nonsense p.Q85* c.253C>T 3 52442492 LUAD G A Nonsense p.R60* c.178C>T 3 52442567 RCCC G C Missense p.A145G c.434C>G 3 52441418 RCCC G C Missense p.I47M c.141C>G 3 52442604 BLCA G C Missense p.L49V c.145C>G 3 52442600 BRCA G C Missense p.L49V c.145C>G 3 52442600 RCCC G C Missense p.S525C c.1574C>G 3 52437587 BRCA G C Nonsense p.S460* c.1379C>G 3 52437782 RCCC G C Nonsense p.Y627* c.1881C>G 3 52437163 RCCC GCTGCCTGGAGGCTTCACCA - Frameshift p.V335Efs*56 c.1004_1023delTGGTGAAGCCTCCAGGCAGC 3 52439219 RCCC G - Frameshift p.R717Gfs*146 c.2149delC 3 52436345 RCCC G T Missense p.P588T c.1762C>A 3 52437282 ESCA G T Nonsense p.S279* c.836C>A 3 52439876 RCCC TAAAGGTGCAGATGAACTCATCGTAG - Frameshift p.Y671Lfs*37 c.2010_2035delCTACGATGAGTTCATCTGCACCTTTA 3 52436639 BRCA T A Missense p.K612M c.1835A>T 3 52437209 CM T A Nonsense p.K626* c.1876A>T 3 52437168 RCCC TCAC - Frameshift p.V77Ifs*9 c.229_232delGTGA 3 52442513 RCCC T C CdsStartSNV . c.1A>G 3 52443894 RCCC T C Missense p.D75G c.224A>G 3 52442521 RCCC T C Missense p.E242G c.725A>G 3 52440327 GBM T C Missense p.E31G c.92A>G 3 52443600 THCA T C Missense p.M211V c.631A>G 3 52440873 UCEC T C Missense p.N344S c.1031A>G 3 52439211 CLL T C Missense p.N78S c.233A>G 3 52442512 RCCC T C SpliceAcceptorSNV . c.932-2A>G 3 52439312 RCCC T - Frameshift p.D407Vfs*23 c.1220delA 3 52438499 RCCC T - Frameshift p.E283Gfs*52 c.848delA 3 52439864 RCCC T - Frameshift p.K711Sfs*152 c.2132delA 3 52436362 RCCC TG - Frameshift p.Q267Afs*16 c.799_800delCA 3 52439912 HNSC T G Missense p.E31A c.92A>C 3 52443600 RCCC T G Missense p.I586L c.1756A>C 3 52437288 HNSC T G Missense p.N229H c.685A>C 3 52440367 RCCC A C Missense p.E86D c.258A>C 1 185062202 BRCA A C Missense p.H123P c.368A>C 1 185062312 COREAD A G Missense p.N209D c.625A>G 1 185067364 CM A T Missense p.I53F c.157A>T 1 185060780 LUAD C A Synonymous p.T292T c.876C>A 1 185069061 CM C G Missense p.H46D c.136C>G 1 185060759 SCLC C T Missense p.H123Y c.367C>T 1 185062311 HNSC C T Missense p.P115S c.343C>T 1 185062287 CM C T Missense p.P12S c.34C>T 1 185056719 CM C T Synonymous p.G300G c.900C>T 1 185069085 ESCA C T Synonymous p.I110I c.330C>T 1 185062274 MM C T Synonymous p.L45L c.133C>T 1 185060756 BRCA C T Synonymous p.N253N c.759C>T 1 185068944 STAD C T Synonymous p.T61T c.183C>T 1 185060806 NB G A Missense p.D34N c.100G>A 1 185060723 CM G A Missense p.G83D c.248G>A 1 185060871 UCEC G A Missense p.S274N c.821G>A 1 185069006 GBM G A Nonsense p.W17* c.50G>A 1 185056735 BLCA G C Missense p.E125D c.375G>C 1 185062319 BRCA G C Missense p.L58F c.174G>C 1 185060797 THCA G T Missense p.G307V c.920G>T 1 185069342 LUAD T A IntronicSNV . c.248+90T>A 1 185060961 CM T C 3-UTRSNV . c.1008+1766T>C 1 185071196 DLBCL T C Missense p.Y120H c.358T>C 1 185062302 CM