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 16 3843582 3843582 + Missense_Mutation SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr16:3843582C>A c.1021G>T c.(1021-1023)Gca>Tca p.A341S BLCA 16 3777746 3777746 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr16:3777746C>T c.7302G>A c.(7300-7302)acG>acA p.T2434T BLCA 16 3777906 3777906 + Missense_Mutation SNP C C A TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr16:3777906C>A c.7142G>T c.(7141-7143)gGt>gTt p.G2381V BLCA 16 3777907 3777907 + Missense_Mutation SNP C C A TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr16:3777907C>A c.7141G>T c.(7141-7143)Ggt>Tgt p.G2381C BLCA 16 3778370 3778370 + Silent SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr16:3778370C>T c.6678G>A c.(6676-6678)gcG>gcA p.A2226A BLCA 16 3778456 3778468 + Frame_Shift_Del DEL GCAGCTGCCTCCG GCAGCTGCCTCCG - TCGA-DK-A6B0-01A-11D-A31L-08 TCGA-DK-A6B0-10A-01D-A31J-08 g.chr16:3778456_3778468delGCAGCTGCCTCCG c.6580_6592delCGGAGGCAGCTGC c.(6580-6594)cggaggcagctgctgfs p.RRQLL2194fs BLCA 16 3779153 3779153 + Silent SNP C C T TCGA-GV-A3JV-01A-11D-A21Z-08 TCGA-GV-A3JV-10B-01D-A21Z-08 g.chr16:3779153C>T c.5895G>A c.(5893-5895)gaG>gaA p.E1965E BLCA 16 3779158 3779158 + Missense_Mutation SNP G G A TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr16:3779158G>A c.5890C>T c.(5890-5892)Cgt>Tgt p.R1964C BLCA 16 3779343 3779343 + Missense_Mutation SNP G G A TCGA-KQ-A41O-01A-12D-A34U-08 TCGA-KQ-A41O-10D-01D-A34X-08 g.chr16:3779343G>A c.5705C>T c.(5704-5706)aCg>aTg p.T1902M BLCA 16 3779715 3779715 + Nonsense_Mutation SNP G G T TCGA-FJ-A871-01A-11D-A34U-08 TCGA-FJ-A871-10A-01D-A34X-08 g.chr16:3779715G>T c.5333C>A c.(5332-5334)tCg>tAg p.S1778* BLCA 16 3781305 3781305 + Missense_Mutation SNP G G A TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr16:3781305G>A c.5060C>T c.(5059-5061)tCc>tTc p.S1687F BLCA 16 3781324 3781326 + In_Frame_Del DEL AGG AGG - TCGA-FJ-A3Z9-01A-11D-A26M-08 TCGA-FJ-A3Z9-10A-01D-A26K-08 g.chr16:3781324_3781326delAGG c.5039_5041delCCT c.(5038-5043)tccttg>ttg p.S1680del BLCA 16 3781375 3781375 + Missense_Mutation SNP G G A TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr16:3781375G>A c.4990C>T c.(4990-4992)Cgc>Tgc p.R1664C BLCA 16 3786148 3786148 + Nonsense_Mutation SNP A A C TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr16:3786148A>C c.4617T>G c.(4615-4617)taT>taG p.Y1539* BLCA 16 3786650 3786650 + Splice_Site SNP C C T TCGA-4Z-AA81-01A-11D-A391-08 TCGA-4Z-AA81-10A-01D-A394-08 g.chr16:3786650C>T c.e27+1 BLCA 16 3786659 3786659 + Missense_Mutation SNP C C T TCGA-E7-A7PW-01A-11D-A34U-08 TCGA-E7-A7PW-10A-01D-A34X-08 g.chr16:3786659C>T c.4552G>A c.(4552-4554)Gac>Aac p.D1518N BLCA 16 3786703 3786703 + Missense_Mutation SNP T T C TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr16:3786703T>C c.4508A>G c.(4507-4509)tAc>tGc p.Y1503C BLCA 16 3786706 3786706 + Nonsense_Mutation SNP C C T TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr16:3786706C>T c.4505G>A c.(4504-4506)tGg>tAg p.W1502* BLCA 16 3786760 3786760 + Missense_Mutation SNP A A G TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr16:3786760A>G c.4451T>C c.(4450-4452)tTc>tCc p.F1484S BLCA 16 3788617 3788617 + Missense_Mutation SNP C C A TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr16:3788617C>A c.4337G>T c.(4336-4338)cGc>cTc p.R1446L BLCA 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-FD-A3SP-01A-31D-A22Z-08 TCGA-FD-A3SP-10A-01D-A22Z-08 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C BLCA 16 3788647 3788647 + Missense_Mutation SNP C C T TCGA-C4-A0F0-01A-12D-A10S-08 TCGA-C4-A0F0-10A-01D-A10S-08 g.chr16:3788647C>T c.4307G>A c.(4306-4308)aGt>aAt p.S1436N BLCA 16 3788650 3788650 + Missense_Mutation SNP T T C TCGA-ZF-A9RN-01A-11D-A42E-08 TCGA-ZF-A9RN-10A-01D-A42H-08 g.chr16:3788650T>C c.4304A>G c.(4303-4305)gAt>gGt p.D1435G BLCA 16 3788651 3788651 + Missense_Mutation SNP C C A TCGA-BL-A5ZZ-01A-31D-A30E-08 TCGA-BL-A5ZZ-10A-01D-A30H-08 g.chr16:3788651C>A c.4303G>T c.(4303-4305)Gat>Tat p.D1435Y BLCA 16 3788651 3788651 + Missense_Mutation SNP C C G TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr16:3788651C>G c.4303G>C c.(4303-4305)Gat>Cat p.D1435H BLCA 16 3788651 3788651 + Missense_Mutation SNP C C G TCGA-FD-A3SL-01A-21D-A22Z-08 TCGA-FD-A3SL-10A-01D-A22Z-08 g.chr16:3788651C>G c.4303G>C c.(4303-4305)Gat>Cat p.D1435H BLCA 16 3788653 3788653 + Missense_Mutation SNP A A C TCGA-ZF-AA4R-01A-11D-A38G-08 TCGA-ZF-AA4R-10A-01D-A38J-08 g.chr16:3788653A>C c.4301T>G c.(4300-4302)cTg>cGg p.L1434R BLCA 16 3789685 3789685 + Nonsense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:3789685G>A c.4174C>T c.(4174-4176)Cga>Tga p.R1392* BLCA 16 3795301 3795301 + Silent SNP G G A TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr16:3795301G>A c.3891C>T c.(3889-3891)caC>caT p.H1297H BLCA 16 3799627 3799627 + Splice_Site SNP C C T TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr16:3799627C>T c.e21+1 BLCA 16 3799671 3799671 + Missense_Mutation SNP C C G TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr16:3799671C>G c.3793G>C c.(3793-3795)Gat>Cat p.D1265H BLCA 16 3807879 3807879 + Missense_Mutation SNP C C G TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr16:3807879C>G c.3540G>C c.(3538-3540)aaG>aaC p.K1180N BLCA 16 3807965 3807965 + Nonsense_Mutation SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr16:3807965G>A c.3454C>T c.(3454-3456)Cag>Tag p.Q1152* BLCA 16 3807992 3807992 + Missense_Mutation SNP C C G TCGA-GV-A3QG-01A-11D-A21Z-08 TCGA-GV-A3QG-10A-01D-A21Z-08 g.chr16:3807992C>G c.3427G>C c.(3427-3429)Gac>Cac p.D1143H BLCA 16 3808023 3808023 + Silent SNP G G A TCGA-4Z-AA82-01A-11D-A391-08 TCGA-4Z-AA82-10A-01D-A394-08 g.chr16:3808023G>A c.3396C>T c.(3394-3396)ccC>ccT p.P1132P BLCA 16 3808853 3808853 + Splice_Site SNP A A T TCGA-XF-AAMT-01A-11D-A42E-08 TCGA-XF-AAMT-10A-01D-A42H-08 g.chr16:3808853A>T c.e17+1 BLCA 16 3817738 3817738 + Nonsense_Mutation SNP G G T TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr16:3817738G>T c.3233C>A c.(3232-3234)tCg>tAg p.S1078* BLCA 16 3817750 3817750 + Nonsense_Mutation SNP G G C TCGA-BT-A20O-01A-21D-A14W-08 TCGA-BT-A20O-11A-11D-A14W-08 g.chr16:3817750G>C c.3221C>G c.(3220-3222)tCa>tGa p.S1074* BLCA 16 3819201 3819201 + Missense_Mutation SNP C C T TCGA-FD-A3SM-01A-11D-A22Z-08 TCGA-FD-A3SM-10A-01D-A22Z-08 g.chr16:3819201C>T c.3034G>A c.(3034-3036)Gaa>Aaa p.E1012K BLCA 16 3819231 3819231 + Frame_Shift_Del DEL G G - TCGA-E7-A519-01A-11D-A26M-08 TCGA-E7-A519-10A-01D-A26K-08 g.chr16:3819231delG c.3004delC c.(3004-3006)caafs p.Q1002fs BLCA 16 3820720 3820720 + Nonsense_Mutation SNP G G A TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr16:3820720G>A c.2731C>T c.(2731-2733)Caa>Taa p.Q911* BLCA 16 3820785 3820785 + Nonsense_Mutation SNP G G C TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr16:3820785G>C c.2666C>G c.(2665-2667)tCa>tGa p.S889* BLCA 16 3820792 3820792 + Nonsense_Mutation SNP G G A TCGA-BT-A20T-01A-11D-A14W-08 TCGA-BT-A20T-11A-11D-A14W-08 g.chr16:3820792G>A c.2659C>T c.(2659-2661)Cag>Tag p.Q887* BLCA 16 3820936 3820936 + Nonsense_Mutation SNP G G A TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr16:3820936G>A c.2515C>T c.(2515-2517)Cag>Tag p.Q839* BLCA 16 3820952 3820952 + Silent SNP G G C TCGA-BT-A20T-01A-11D-A14W-08 TCGA-BT-A20T-11A-11D-A14W-08 g.chr16:3820952G>C c.2499C>G c.(2497-2499)ctC>ctG p.L833L BLCA 16 3823904 3823904 + Nonsense_Mutation SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr16:3823904G>A c.2311C>T c.(2311-2313)Cag>Tag p.Q771* BLCA 16 3824685 3824685 + Nonsense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:3824685G>T c.2168C>A c.(2167-2169)tCa>tAa p.S723* BLCA 16 3824690 3824690 + Missense_Mutation SNP C C T TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr16:3824690C>T c.2163G>A c.(2161-2163)atG>atA p.M721I BLCA 16 3828043 3828043 + Silent SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr16:3828043C>T c.2082G>A c.(2080-2082)gtG>gtA p.V694V BLCA 16 3828045 3828045 + Missense_Mutation SNP C C G TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr16:3828045C>G c.2080G>C c.(2080-2082)Gtg>Ctg p.V694L BLCA 16 3828084 3828085 + Frame_Shift_Ins INS - - C TCGA-GC-A3RD-01A-12D-A22Z-08 TCGA-GC-A3RD-10B-01D-A22Z-08 g.chr16:3828084_3828085insC c.2040_2041insG c.(2038-2043)gggaacfs p.N681fs BLCA 16 3828129 3828129 + Missense_Mutation SNP C C G TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr16:3828129C>G c.1996G>C c.(1996-1998)Gaa>Caa p.E666Q BLCA 16 3828757 3828778 + Frame_Shift_Del DEL GGTTTTCCATGCGGCGATCCTT GGTTTTCCATGCGGCGATCCTT - TCGA-CF-A9FL-01A-11D-A38G-08 TCGA-CF-A9FL-10A-01D-A38J-08 g.chr16:3828757_3828778delGGTTTTCCATGCGGCGATCCTT c.1864_1885delAAGGATCGCCGCATGGAAAACC c.(1864-1887)aaggatcgccgcatggaaaacctgfs p.KDRRMENL622fs BLCA 16 3830776 3830776 + Nonsense_Mutation SNP C C A TCGA-E7-A6ME-01A-22D-A32B-08 TCGA-E7-A6ME-10B-01D-A329-08 g.chr16:3830776C>A c.1780G>T c.(1780-1782)Gaa>Taa p.E594* BLCA 16 3831263 3831263 + Nonsense_Mutation SNP G G A TCGA-K4-AAQO-01A-11D-A38G-08 TCGA-K4-AAQO-10A-01D-A38J-08 g.chr16:3831263G>A c.1618C>T c.(1618-1620)Cag>Tag p.Q540* BLCA 16 3831263 3831263 + Nonsense_Mutation SNP G G A TCGA-ZF-A9RG-01A-21D-A42E-08 TCGA-ZF-A9RG-10A-01D-A42H-08 g.chr16:3831263G>A c.1618C>T c.(1618-1620)Cag>Tag p.Q540* BLCA 16 3841997 3841997 + Nonsense_Mutation SNP T T A TCGA-PQ-A6FI-01A-11D-A31L-08 TCGA-PQ-A6FI-10A-01D-A31J-08 g.chr16:3841997T>A c.1315A>T c.(1315-1317)Aag>Tag p.K439* BLCA 16 3900804 3900804 + Missense_Mutation SNP C C A TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr16:3900804C>A c.292G>T c.(292-294)Ggc>Tgc p.G98C BLCA 16 3900805 3900805 + Silent SNP C C T TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr16:3900805C>T c.291G>A c.(289-291)caG>caA p.Q97Q BLCA 16 3900861 3900861 + Missense_Mutation SNP C C T TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr16:3900861C>T c.235G>A c.(235-237)Ggc>Agc p.G79S BRCA 16 3777933 3777933 + Missense_Mutation SNP G G A TCGA-C8-A26V-01A-11D-A16D-09 TCGA-C8-A26V-10A-01D-A16D-09 g.chr16:3777933G>A c.7115C>T c.(7114-7116)tCg>tTg p.S2372L BRCA 16 3778245 3778245 + Missense_Mutation SNP A A G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr16:3778245A>G c.6803T>C c.(6802-6804)aTg>aCg p.M2268T BRCA 16 3778745 3778745 + Missense_Mutation SNP G G C TCGA-BH-A0W7-01A-11D-A10Y-09 TCGA-BH-A0W7-10A-01D-A110-09 g.chr16:3778745G>C c.6303C>G c.(6301-6303)atC>atG p.I2101M BRCA 16 3778897 3778898 + Frame_Shift_Ins INS - - C TCGA-AN-A0AR-01A-11W-A019-09 TCGA-AN-A0AR-10A-01W-A021-09 g.chr16:3778897_3778898insC c.6150_6151insG c.(6148-6153)gggcccfs p.P2051fs BRCA 16 3779066 3779066 + Missense_Mutation SNP C C G TCGA-D8-A27H-01A-11D-A16D-09 TCGA-D8-A27H-10A-01D-A16D-09 g.chr16:3779066C>G c.5982G>C c.(5980-5982)caG>caC p.Q1994H BRCA 16 3779642 3779642 + Silent SNP C C G TCGA-A8-A097-01A-11W-A050-09 TCGA-A8-A097-10A-01D-A047-09 g.chr16:3779642C>G c.5406G>C c.(5404-5406)gtG>gtC p.V1802V BRCA 16 3781302 3781302 + Missense_Mutation SNP G G A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr16:3781302G>A c.5063C>T c.(5062-5064)aCg>aTg p.T1688M BRCA 16 3781803 3781803 + Missense_Mutation SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr16:3781803A>G c.4864T>C c.(4864-4866)Tat>Cat p.Y1622H BRCA 16 3781889 3781889 + Missense_Mutation SNP G G T TCGA-B6-A1KF-01A-11D-A13L-09 TCGA-B6-A1KF-10A-01W-A14R-09 g.chr16:3781889G>T c.4778C>A c.(4777-4779)aCc>aAc p.T1593N BRCA 16 3789684 3789684 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr16:3789684C>T c.4175G>A c.(4174-4176)cGa>cAa p.R1392Q BRCA 16 3795332 3795332 + Missense_Mutation SNP C C T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr16:3795332C>T c.3860G>A c.(3859-3861)gGc>gAc p.G1287D BRCA 16 3807914 3807914 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr16:3807914G>A c.3505C>T c.(3505-3507)Cgc>Tgc p.R1169C BRCA 16 3808953 3808953 + Missense_Mutation SNP G G A TCGA-C8-A1HE-01A-11D-A188-09 TCGA-C8-A1HE-10A-01D-A13O-09 g.chr16:3808953G>A c.3271C>T c.(3271-3273)Cgc>Tgc p.R1091C BRCA 16 3823824 3823825 + Frame_Shift_Ins INS - - T TCGA-AN-A0AT-01A-11D-A045-09 TCGA-AN-A0AT-10A-01W-A055-09 g.chr16:3823824_3823825insT c.2390_2391insA c.(2389-2391)aacfs p.N797fs BRCA 16 3827658 3827658 + Splice_Site SNP T T C TCGA-A2-A1G1-01A-21D-A13L-09 TCGA-A2-A1G1-10A-01D-A13O-09 g.chr16:3827658T>C c.2114A>G c.(2113-2115)aAt>aGt p.N705S BRCA 16 3900518 3900518 + Missense_Mutation SNP G G C TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr16:3900518G>C c.578C>G c.(577-579)tCt>tGt p.S193C BRCA 16 3900661 3900661 + Silent SNP G G T TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr16:3900661G>T c.435C>A c.(433-435)ccC>ccA p.P145P BRCA 16 3900736 3900736 + Silent SNP C C T TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr16:3900736C>T c.360G>A c.(358-360)aaG>aaA p.K120K CESC 16 3778628 3778628 + Silent SNP C C T TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr16:3778628C>T c.6420G>A c.(6418-6420)caG>caA p.Q2140Q CESC 16 3779771 3779771 + Silent SNP T T A TCGA-EA-A3QD-01A-32D-A22X-09 TCGA-EA-A3QD-10A-01D-A22X-09 g.chr16:3779771T>A c.5277A>T c.(5275-5277)ccA>ccT p.P1759P CESC 16 3781798 3781798 + Silent SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr16:3781798G>T c.4869C>A c.(4867-4869)gcC>gcA p.A1623A CESC 16 3786138 3786138 + Missense_Mutation SNP C C G TCGA-EA-A1QT-01A-11D-A14W-08 TCGA-EA-A1QT-10A-01D-A14W-08 g.chr16:3786138C>G c.4627G>C c.(4627-4629)Gat>Cat p.D1543H CESC 16 3786748 3786748 + Missense_Mutation SNP G G C TCGA-C5-A2LX-01A-11D-A18J-09 TCGA-C5-A2LX-10A-01D-A18J-09 g.chr16:3786748G>C c.4463C>G c.(4462-4464)cCa>cGa p.P1488R CESC 16 3786798 3786798 + Missense_Mutation SNP G G C TCGA-DG-A2KM-01A-11D-A17W-09 TCGA-DG-A2KM-10A-01D-A17W-09 g.chr16:3786798G>C c.4413C>G c.(4411-4413)atC>atG p.I1471M CESC 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C CESC 16 3794922 3794922 + Nonsense_Mutation SNP G G A TCGA-EK-A2RC-01A-11D-A18J-09 TCGA-EK-A2RC-10A-01D-A18J-09 g.chr16:3794922G>A c.3955C>T c.(3955-3957)Cga>Tga p.R1319* CESC 16 3799625 3799626 + Intron INS - - A TCGA-Q1-A6DV-01A-11D-A32I-09 TCGA-Q1-A6DV-10A-01D-A32I-09 g.chr16:3799625_3799626insA CESC 16 3801726 3801726 + Splice_Site SNP C C T TCGA-FU-A3TX-01A-11D-A22X-09 TCGA-FU-A3TX-10A-01D-A22X-09 g.chr16:3801726C>T c.e20+1 CESC 16 3817784 3817784 + Nonsense_Mutation SNP C C A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr16:3817784C>A c.3187G>T c.(3187-3189)Gaa>Taa p.E1063* CESC 16 3817799 3817799 + Nonsense_Mutation SNP C C A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr16:3817799C>A c.3172G>T c.(3172-3174)Gaa>Taa p.E1058* CESC 16 3900422 3900422 + Missense_Mutation SNP G G A TCGA-C5-A1BJ-01A-11D-A13W-08 TCGA-C5-A1BJ-10A-01D-A13W-08 g.chr16:3900422G>A c.674C>T c.(673-675)cCg>cTg p.P225L CESC 16 3900459 3900459 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr16:3900459G>A c.637C>T c.(637-639)Ctt>Ttt p.L213F CESC 16 3900710 3900710 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr16:3900710G>A c.386C>T c.(385-387)tCa>tTa p.S129L CESC 16 3900710 3900710 + Nonsense_Mutation SNP G G T TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr16:3900710G>T c.386C>A c.(385-387)tCa>tAa p.S129* CESC 16 3900884 3900884 + Missense_Mutation SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr16:3900884G>A c.212C>T c.(211-213)tCg>tTg p.S71L CESC 16 3900914 3900914 + Missense_Mutation SNP G G A TCGA-FU-A23K-01A-11D-A16O-08 TCGA-FU-A23K-10A-01D-A16O-08 g.chr16:3900914G>A c.182C>T c.(181-183)cCa>cTa p.P61L CESC 16 3901001 3901001 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr16:3901001G>A c.95C>T c.(94-96)tCa>tTa p.S32L COAD 16 3777817 3777817 + Frame_Shift_Del DEL G G - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:3777817delG c.7231delC c.(7231-7233)cagfs p.Q2411fs COAD 16 3777941 3777941 + Silent SNP G G A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr16:3777941G>A c.7107C>T c.(7105-7107)ccC>ccT p.P2369P COAD 16 3778452 3778452 + Missense_Mutation SNP T T A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:3778452T>A c.6596A>T c.(6595-6597)cAg>cTg p.Q2199L COAD 16 3778597 3778597 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr16:3778597G>A c.6451C>T c.(6451-6453)Cgg>Tgg p.R2151W COAD 16 3778833 3778833 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr16:3778833C>T c.6215G>A c.(6214-6216)cGg>cAg p.R2072Q COAD 16 3778976 3778976 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:3778976C>T c.6072G>A c.(6070-6072)gcG>gcA p.A2024A COAD 16 3779278 3779278 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:3779278C>T c.5770G>A c.(5770-5772)Gtg>Atg p.V1924M COAD 16 3779387 3779387 + Silent SNP T T C TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr16:3779387T>C c.5661A>G c.(5659-5661)tcA>tcG p.S1887S COAD 16 3779388 3779388 + Nonsense_Mutation SNP G G T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr16:3779388G>T c.5660C>A c.(5659-5661)tCa>tAa p.S1887* COAD 16 3779534 3779534 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr16:3779534G>A c.5514C>T c.(5512-5514)tgC>tgT p.C1838C COAD 16 3779624 3779624 + Nonsense_Mutation SNP G G T TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chr16:3779624G>T c.5424C>A c.(5422-5424)tgC>tgA p.C1808* COAD 16 3779766 3779766 + Nonsense_Mutation SNP G G T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr16:3779766G>T c.5282C>A c.(5281-5283)tCa>tAa p.S1761* COAD 16 3779829 3779829 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3779829T>C c.5219A>G c.(5218-5220)cAt>cGt p.H1740R COAD 16 3779844 3779844 + Missense_Mutation SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3779844G>A c.5204C>T c.(5203-5205)aCg>aTg p.T1735M COAD 16 3781278 3781278 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3781278T>C c.5087A>G c.(5086-5088)cAc>cGc p.H1696R COAD 16 3781301 3781301 + Silent SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr16:3781301C>T c.5064G>A c.(5062-5064)acG>acA p.T1688T COAD 16 3781317 3781317 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:3781317C>T c.5048G>A c.(5047-5049)cGc>cAc p.R1683H COAD 16 3781324 3781326 + In_Frame_Del DEL AGG AGG - TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:3781324_3781326delAGG c.5039_5041delCCT c.(5038-5043)tccttg>ttg p.S1680del COAD 16 3781414 3781414 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr16:3781414C>T c.4951G>A c.(4951-4953)Gac>Aac p.D1651N COAD 16 3781472 3781472 + Silent SNP G G T TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr16:3781472G>T c.4893C>A c.(4891-4893)gtC>gtA p.V1631V COAD 16 3781793 3781793 + Missense_Mutation SNP A A G TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr16:3781793A>G c.4874T>C c.(4873-4875)aTg>aCg p.M1625T COAD 16 3781797 3781797 + Missense_Mutation SNP T T G TCGA-AA-3973-01A-01W-0995-10 TCGA-AA-3973-10A-01W-0999-10 g.chr16:3781797T>G c.4870A>C c.(4870-4872)Acc>Ccc p.T1624P COAD 16 3781827 3781827 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3781827A>G c.4840T>C c.(4840-4842)Tcc>Ccc p.S1614P COAD 16 3781830 3781830 + Missense_Mutation SNP C C T TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr16:3781830C>T c.4837G>A c.(4837-4839)Gtg>Atg p.V1613M COAD 16 3781845 3781845 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr16:3781845G>A c.4822C>T c.(4822-4824)Ccc>Tcc p.P1608S COAD 16 3781854 3781854 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:3781854T>C c.4813A>G c.(4813-4815)Aag>Gag p.K1605E COAD 16 3786076 3786076 + Silent SNP C C T TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr16:3786076C>T c.4689G>A c.(4687-4689)agG>agA p.R1563R COAD 16 3786076 3786076 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3786076C>T c.4689G>A c.(4687-4689)agG>agA p.R1563R COAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COAD 16 3786704 3786704 + Missense_Mutation SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr16:3786704A>G c.4507T>C c.(4507-4509)Tac>Cac p.Y1503H COAD 16 3786705 3786705 + Nonsense_Mutation SNP C C T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr16:3786705C>T c.4506G>A c.(4504-4506)tgG>tgA p.W1502* COAD 16 3786712 3786712 + Missense_Mutation SNP T T C TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr16:3786712T>C c.4499A>G c.(4498-4500)cAg>cGg p.Q1500R COAD 16 3786713 3786713 + Nonsense_Mutation SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr16:3786713G>A c.4498C>T c.(4498-4500)Cag>Tag p.Q1500* COAD 16 3786752 3786752 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr16:3786752G>A c.4459C>T c.(4459-4461)Cac>Tac p.H1487Y COAD 16 3786763 3786763 + Missense_Mutation SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3786763A>G c.4448T>C c.(4447-4449)aTc>aCc p.I1483T COAD 16 3786765 3786765 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3786765G>A c.4446C>T c.(4444-4446)taC>taT p.Y1482Y COAD 16 3786766 3786766 + Missense_Mutation SNP T T A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3786766T>A c.4445A>T c.(4444-4446)tAc>tTc p.Y1482F COAD 16 3786766 3786766 + Missense_Mutation SNP T T A TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr16:3786766T>A c.4445A>T c.(4444-4446)tAc>tTc p.Y1482F COAD 16 3786784 3786784 + Missense_Mutation SNP G G A TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr16:3786784G>A c.4427C>T c.(4426-4428)cCa>cTa p.P1476L COAD 16 3788652 3788652 + Silent SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr16:3788652C>A c.4302G>T c.(4300-4302)ctG>ctT p.L1434L COAD 16 3788672 3788672 + Splice_Site SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr16:3788672G>A c.4282C>T c.(4282-4284)Cgt>Tgt p.R1428C COAD 16 3789646 3789646 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:3789646C>T c.4213G>A c.(4213-4215)Gtg>Atg p.V1405M COAD 16 3789693 3789693 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3789693A>G c.4166T>C c.(4165-4167)tTc>tCc p.F1389S COAD 16 3790454 3790454 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:3790454C>T c.4079G>A c.(4078-4080)cGa>cAa p.R1360Q COAD 16 3790455 3790455 + Silent SNP G G T TCGA-A6-2671-01A-01D-1408-10 TCGA-A6-2671-10A-01D-1408-10 g.chr16:3790455G>T c.4078C>A c.(4078-4080)Cga>Aga p.R1360R COAD 16 3790455 3790455 + Silent SNP G G T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3790455G>T c.4078C>A c.(4078-4080)Cga>Aga p.R1360R COAD 16 3790470 3790470 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr16:3790470C>T c.4063G>A c.(4063-4065)Ggg>Agg p.G1355R COAD 16 3790511 3790511 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr16:3790511C>A c.4022G>T c.(4021-4023)cGa>cTa p.R1341L COAD 16 3790512 3790512 + Nonsense_Mutation SNP G G A TCGA-AA-A029-01A-01W-A00E-09 TCGA-AA-A029-10A-01W-A00E-09 g.chr16:3790512G>A c.4021C>T c.(4021-4023)Cga>Tga p.R1341* COAD 16 3790512 3790512 + Silent SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3790512G>T c.4021C>A c.(4021-4023)Cga>Aga p.R1341R COAD 16 3790519 3790519 + Silent SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:3790519C>T c.4014G>A c.(4012-4014)ttG>ttA p.L1338L COAD 16 3790520 3790520 + Missense_Mutation SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr16:3790520A>G c.4013T>C c.(4012-4014)tTg>tCg p.L1338S COAD 16 3790521 3790521 + Silent SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3790521A>G c.4012T>C c.(4012-4014)Ttg>Ctg p.L1338L COAD 16 3794917 3794917 + Silent SNP T T C TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr16:3794917T>C c.3960A>G c.(3958-3960)aaA>aaG p.K1320K COAD 16 3794917 3794917 + Silent SNP T T C TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr16:3794917T>C c.3960A>G c.(3958-3960)aaA>aaG p.K1320K COAD 16 3795310 3795310 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:3795310G>A c.3882C>T c.(3880-3882)tgC>tgT p.C1294C COAD 16 3801786 3801786 + Silent SNP A A G TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr16:3801786A>G c.3720T>C c.(3718-3720)tgT>tgC p.C1240C COAD 16 3801786 3801786 + Silent SNP A A G TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr16:3801786A>G c.3720T>C c.(3718-3720)tgT>tgC p.C1240C COAD 16 3807900 3807900 + Silent SNP T T C TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:3807900T>C c.3519A>G c.(3517-3519)cgA>cgG p.R1173R COAD 16 3807902 3807902 + Nonsense_Mutation SNP G G A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr16:3807902G>A c.3517C>T c.(3517-3519)Cga>Tga p.R1173* COAD 16 3807902 3807902 + Silent SNP G G T TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:3807902G>T c.3517C>A c.(3517-3519)Cga>Aga p.R1173R COAD 16 3807902 3807902 + Silent SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3807902G>T c.3517C>A c.(3517-3519)Cga>Aga p.R1173R COAD 16 3807912 3807912 + Silent SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr16:3807912G>A c.3507C>T c.(3505-3507)cgC>cgT p.R1169R COAD 16 3807914 3807914 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr16:3807914G>A c.3505C>T c.(3505-3507)Cgc>Tgc p.R1169C COAD 16 3807926 3807926 + Missense_Mutation SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:3807926A>G c.3493T>C c.(3493-3495)Tgg>Cgg p.W1165R COAD 16 3808046 3808046 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3808046A>G c.3373T>C c.(3373-3375)Tat>Cat p.Y1125H COAD 16 3808863 3808863 + Nonsense_Mutation SNP C C A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr16:3808863C>A c.3361G>T c.(3361-3363)Gga>Tga p.G1121* COAD 16 3808955 3808955 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3808955A>G c.3269T>C c.(3268-3270)tTa>tCa p.L1090S COAD 16 3808956 3808956 + Silent SNP A A G TCGA-A6-6649-01A-11D-1771-10 TCGA-A6-6649-10A-01D-1771-10 g.chr16:3808956A>G c.3268T>C c.(3268-3270)Tta>Cta p.L1090L COAD 16 3817812 3817812 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:3817812A>G c.3159T>C c.(3157-3159)ccT>ccC p.P1053P COAD 16 3817813 3817813 + Missense_Mutation SNP G G T TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr16:3817813G>T c.3158C>A c.(3157-3159)cCt>cAt p.P1053H COAD 16 3819176 3819176 + Splice_Site SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr16:3819176T>C c.3059A>G c.(3058-3060)gAg>gGg p.E1020G COAD 16 3820640 3820640 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:3820640C>T c.2811G>A c.(2809-2811)ccG>ccA p.P937P COAD 16 3820773 3820773 + Missense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3820773G>A c.2678C>T c.(2677-2679)tCg>tTg p.S893L COAD 16 3820774 3820774 + Missense_Mutation SNP A A G TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr16:3820774A>G c.2677T>C c.(2677-2679)Tcg>Ccg p.S893P COAD 16 3820774 3820774 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:3820774A>G c.2677T>C c.(2677-2679)Tcg>Ccg p.S893P COAD 16 3820934 3820934 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr16:3820934C>A c.2517G>T c.(2515-2517)caG>caT p.Q839H COAD 16 3820935 3820935 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr16:3820935T>C c.2516A>G c.(2515-2517)cAg>cGg p.Q839R COAD 16 3823907 3823907 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr16:3823907G>A c.2308C>T c.(2308-2310)Cct>Tct p.P770S COAD 16 3824575 3824575 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr16:3824575G>A c.2278C>T c.(2278-2280)Cca>Tca p.P760S COAD 16 3824598 3824598 + Missense_Mutation SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr16:3824598T>C c.2255A>G c.(2254-2256)cAg>cGg p.Q752R COAD 16 3824675 3824675 + Silent SNP G G A TCGA-AA-3695-01A-01W-0900-09 TCGA-AA-3695-10A-01W-0900-09 g.chr16:3824675G>A c.2178C>T c.(2176-2178)ccC>ccT p.P726P COAD 16 3824694 3824694 + Splice_Site SNP C C A TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr16:3824694C>A c.2159G>T c.(2158-2160)gGg>gTg p.G720V COAD 16 3828175 3828175 + Nonsense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3828175A>C c.1950T>G c.(1948-1950)taT>taG p.Y650* COAD 16 3828184 3828184 + Splice_Site SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:3828184C>A c.e10-1 COAD 16 3830755 3830755 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:3830755G>A c.1801C>T c.(1801-1803)Cgg>Tgg p.R601W COAD 16 3832829 3832829 + Missense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr16:3832829C>T c.1429G>A c.(1429-1431)Gac>Aac p.D477N COAD 16 3832857 3832857 + Silent SNP G G T TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr16:3832857G>T c.1401C>A c.(1399-1401)gcC>gcA p.A467A COAD 16 3832858 3832858 + Missense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr16:3832858G>A c.1400C>T c.(1399-1401)gCc>gTc p.A467V COAD 16 3841993 3841993 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3841993C>T c.1319G>A c.(1318-1320)cGa>cAa p.R440Q COAD 16 3900336 3900336 + Missense_Mutation SNP C C T TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr16:3900336C>T c.760G>A c.(760-762)Gcg>Acg p.A254T COAD 16 3900430 3900430 + Silent SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr16:3900430A>G c.666T>C c.(664-666)gcT>gcC p.A222A COAD 16 3900435 3900435 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3900435C>T c.661G>A c.(661-663)Gga>Aga p.G221R COAD 16 3900630 3900630 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:3900630G>T c.466C>A c.(466-468)Caa>Aaa p.Q156K COAD 16 3900697 3900697 + Silent SNP C C G TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:3900697C>G c.399G>C c.(397-399)ctG>ctC p.L133L COAD 16 3900740 3900740 + Missense_Mutation SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:3900740C>A c.356G>T c.(355-357)gGc>gTc p.G119V COAD 16 3900826 3900826 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3900826G>A c.270C>T c.(268-270)agC>agT p.S90S COAD 16 3900872 3900872 + Missense_Mutation SNP C C A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3900872C>A c.224G>T c.(223-225)cGa>cTa p.R75L COADREAD 16 3777817 3777817 + Frame_Shift_Del DEL G G - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:3777817delG c.7231delC c.(7231-7233)cagfs p.Q2411fs COADREAD 16 3777941 3777941 + Silent SNP G G A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr16:3777941G>A c.7107C>T c.(7105-7107)ccC>ccT p.P2369P COADREAD 16 3778018 3778018 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3778018G>A c.7030C>T c.(7030-7032)Cgg>Tgg p.R2344W COADREAD 16 3778452 3778452 + Missense_Mutation SNP T T A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:3778452T>A c.6596A>T c.(6595-6597)cAg>cTg p.Q2199L COADREAD 16 3778597 3778597 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr16:3778597G>A c.6451C>T c.(6451-6453)Cgg>Tgg p.R2151W COADREAD 16 3778833 3778833 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr16:3778833C>T c.6215G>A c.(6214-6216)cGg>cAg p.R2072Q COADREAD 16 3778976 3778976 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr16:3778976C>T c.6072G>A c.(6070-6072)gcG>gcA p.A2024A COADREAD 16 3779278 3779278 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:3779278C>T c.5770G>A c.(5770-5772)Gtg>Atg p.V1924M COADREAD 16 3779387 3779387 + Silent SNP T T C TCGA-AF-6672-01A-11D-1826-10 TCGA-AF-6672-10A-01D-1826-10 g.chr16:3779387T>C c.5661A>G c.(5659-5661)tcA>tcG p.S1887S COADREAD 16 3779387 3779387 + Silent SNP T T C TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr16:3779387T>C c.5661A>G c.(5659-5661)tcA>tcG p.S1887S COADREAD 16 3779388 3779388 + Nonsense_Mutation SNP G G T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr16:3779388G>T c.5660C>A c.(5659-5661)tCa>tAa p.S1887* COADREAD 16 3779534 3779534 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr16:3779534G>A c.5514C>T c.(5512-5514)tgC>tgT p.C1838C COADREAD 16 3779578 3779578 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3779578C>T c.5470G>A c.(5470-5472)Gcc>Acc p.A1824T COADREAD 16 3779624 3779624 + Nonsense_Mutation SNP G G T TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chr16:3779624G>T c.5424C>A c.(5422-5424)tgC>tgA p.C1808* COADREAD 16 3779766 3779766 + Nonsense_Mutation SNP G G T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr16:3779766G>T c.5282C>A c.(5281-5283)tCa>tAa p.S1761* COADREAD 16 3779829 3779829 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3779829T>C c.5219A>G c.(5218-5220)cAt>cGt p.H1740R COADREAD 16 3779844 3779844 + Missense_Mutation SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3779844G>A c.5204C>T c.(5203-5205)aCg>aTg p.T1735M COADREAD 16 3781278 3781278 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3781278T>C c.5087A>G c.(5086-5088)cAc>cGc p.H1696R COADREAD 16 3781301 3781301 + Silent SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr16:3781301C>T c.5064G>A c.(5062-5064)acG>acA p.T1688T COADREAD 16 3781317 3781317 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:3781317C>T c.5048G>A c.(5047-5049)cGc>cAc p.R1683H COADREAD 16 3781324 3781326 + In_Frame_Del DEL AGG AGG - TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:3781324_3781326delAGG c.5039_5041delCCT c.(5038-5043)tccttg>ttg p.S1680del COADREAD 16 3781414 3781414 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr16:3781414C>T c.4951G>A c.(4951-4953)Gac>Aac p.D1651N COADREAD 16 3781472 3781472 + Silent SNP G G T TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr16:3781472G>T c.4893C>A c.(4891-4893)gtC>gtA p.V1631V COADREAD 16 3781793 3781793 + Missense_Mutation SNP A A G TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr16:3781793A>G c.4874T>C c.(4873-4875)aTg>aCg p.M1625T COADREAD 16 3781797 3781797 + Missense_Mutation SNP T T G TCGA-AA-3973-01A-01W-0995-10 TCGA-AA-3973-10A-01W-0999-10 g.chr16:3781797T>G c.4870A>C c.(4870-4872)Acc>Ccc p.T1624P COADREAD 16 3781827 3781827 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3781827A>G c.4840T>C c.(4840-4842)Tcc>Ccc p.S1614P COADREAD 16 3781830 3781830 + Missense_Mutation SNP C C T TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr16:3781830C>T c.4837G>A c.(4837-4839)Gtg>Atg p.V1613M COADREAD 16 3781845 3781845 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr16:3781845G>A c.4822C>T c.(4822-4824)Ccc>Tcc p.P1608S COADREAD 16 3781854 3781854 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr16:3781854T>C c.4813A>G c.(4813-4815)Aag>Gag p.K1605E COADREAD 16 3786076 3786076 + Silent SNP C C T TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr16:3786076C>T c.4689G>A c.(4687-4689)agG>agA p.R1563R COADREAD 16 3786076 3786076 + Silent SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3786076C>T c.4689G>A c.(4687-4689)agG>agA p.R1563R COADREAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AH-6549-01A-11D-1826-10 TCGA-AH-6549-10A-01D-1826-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COADREAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AH-6643-01A-11D-1826-10 TCGA-AH-6643-11A-01D-1826-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COADREAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COADREAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COADREAD 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G COADREAD 16 3786704 3786704 + Missense_Mutation SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr16:3786704A>G c.4507T>C c.(4507-4509)Tac>Cac p.Y1503H COADREAD 16 3786705 3786705 + Nonsense_Mutation SNP C C T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr16:3786705C>T c.4506G>A c.(4504-4506)tgG>tgA p.W1502* COADREAD 16 3786712 3786712 + Missense_Mutation SNP T T C TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr16:3786712T>C c.4499A>G c.(4498-4500)cAg>cGg p.Q1500R COADREAD 16 3786713 3786713 + Nonsense_Mutation SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr16:3786713G>A c.4498C>T c.(4498-4500)Cag>Tag p.Q1500* COADREAD 16 3786752 3786752 + Missense_Mutation SNP G G A TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr16:3786752G>A c.4459C>T c.(4459-4461)Cac>Tac p.H1487Y COADREAD 16 3786763 3786763 + Missense_Mutation SNP A A G TCGA-F5-6812-01A-11D-1826-10 TCGA-F5-6812-10A-01D-1826-10 g.chr16:3786763A>G c.4448T>C c.(4447-4449)aTc>aCc p.I1483T COADREAD 16 3786763 3786763 + Missense_Mutation SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3786763A>G c.4448T>C c.(4447-4449)aTc>aCc p.I1483T COADREAD 16 3786765 3786765 + Silent SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3786765G>A c.4446C>T c.(4444-4446)taC>taT p.Y1482Y COADREAD 16 3786766 3786766 + Missense_Mutation SNP T T A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3786766T>A c.4445A>T c.(4444-4446)tAc>tTc p.Y1482F COADREAD 16 3786766 3786766 + Missense_Mutation SNP T T A TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr16:3786766T>A c.4445A>T c.(4444-4446)tAc>tTc p.Y1482F COADREAD 16 3786783 3786783 + Silent SNP T T A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:3786783T>A c.4428A>T c.(4426-4428)ccA>ccT p.P1476P COADREAD 16 3786784 3786784 + Missense_Mutation SNP G G A TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr16:3786784G>A c.4427C>T c.(4426-4428)cCa>cTa p.P1476L COADREAD 16 3788618 3788618 + Missense_Mutation SNP G G T TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr16:3788618G>T c.4336C>A c.(4336-4338)Cgc>Agc p.R1446S COADREAD 16 3788652 3788652 + Silent SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr16:3788652C>A c.4302G>T c.(4300-4302)ctG>ctT p.L1434L COADREAD 16 3788672 3788672 + Splice_Site SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr16:3788672G>A c.4282C>T c.(4282-4284)Cgt>Tgt p.R1428C COADREAD 16 3789646 3789646 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:3789646C>T c.4213G>A c.(4213-4215)Gtg>Atg p.V1405M COADREAD 16 3789693 3789693 + Missense_Mutation SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3789693A>G c.4166T>C c.(4165-4167)tTc>tCc p.F1389S COADREAD 16 3789726 3789726 + Splice_Site SNP C C T TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr16:3789726C>T c.e25-1 COADREAD 16 3790454 3790454 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:3790454C>T c.4079G>A c.(4078-4080)cGa>cAa p.R1360Q COADREAD 16 3790455 3790455 + Silent SNP G G T TCGA-A6-2671-01A-01D-1408-10 TCGA-A6-2671-10A-01D-1408-10 g.chr16:3790455G>T c.4078C>A c.(4078-4080)Cga>Aga p.R1360R COADREAD 16 3790455 3790455 + Silent SNP G G T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3790455G>T c.4078C>A c.(4078-4080)Cga>Aga p.R1360R COADREAD 16 3790470 3790470 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr16:3790470C>T c.4063G>A c.(4063-4065)Ggg>Agg p.G1355R COADREAD 16 3790511 3790511 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr16:3790511C>A c.4022G>T c.(4021-4023)cGa>cTa p.R1341L COADREAD 16 3790511 3790511 + Missense_Mutation SNP C C A TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr16:3790511C>A c.4022G>T c.(4021-4023)cGa>cTa p.R1341L COADREAD 16 3790512 3790512 + Nonsense_Mutation SNP G G A TCGA-AA-A029-01A-01W-A00E-09 TCGA-AA-A029-10A-01W-A00E-09 g.chr16:3790512G>A c.4021C>T c.(4021-4023)Cga>Tga p.R1341* COADREAD 16 3790512 3790512 + Silent SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3790512G>T c.4021C>A c.(4021-4023)Cga>Aga p.R1341R COADREAD 16 3790519 3790519 + Silent SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:3790519C>T c.4014G>A c.(4012-4014)ttG>ttA p.L1338L COADREAD 16 3790520 3790520 + Missense_Mutation SNP A A G TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr16:3790520A>G c.4013T>C c.(4012-4014)tTg>tCg p.L1338S COADREAD 16 3790521 3790521 + Silent SNP A A G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3790521A>G c.4012T>C c.(4012-4014)Ttg>Ctg p.L1338L COADREAD 16 3794917 3794917 + Silent SNP T T C TCGA-A6-6654-01A-21D-1835-10 TCGA-A6-6654-10A-01D-1835-10 g.chr16:3794917T>C c.3960A>G c.(3958-3960)aaA>aaG p.K1320K COADREAD 16 3794917 3794917 + Silent SNP T T C TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr16:3794917T>C c.3960A>G c.(3958-3960)aaA>aaG p.K1320K COADREAD 16 3795310 3795310 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:3795310G>A c.3882C>T c.(3880-3882)tgC>tgT p.C1294C COADREAD 16 3801731 3801731 + Nonsense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:3801731G>A c.3775C>T c.(3775-3777)Cag>Tag p.Q1259* COADREAD 16 3801786 3801786 + Silent SNP A A G TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr16:3801786A>G c.3720T>C c.(3718-3720)tgT>tgC p.C1240C COADREAD 16 3801786 3801786 + Silent SNP A A G TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr16:3801786A>G c.3720T>C c.(3718-3720)tgT>tgC p.C1240C COADREAD 16 3807900 3807900 + Silent SNP T T C TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:3807900T>C c.3519A>G c.(3517-3519)cgA>cgG p.R1173R COADREAD 16 3807902 3807902 + Nonsense_Mutation SNP G G A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr16:3807902G>A c.3517C>T c.(3517-3519)Cga>Tga p.R1173* COADREAD 16 3807902 3807902 + Silent SNP G G T TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:3807902G>T c.3517C>A c.(3517-3519)Cga>Aga p.R1173R COADREAD 16 3807902 3807902 + Silent SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3807902G>T c.3517C>A c.(3517-3519)Cga>Aga p.R1173R COADREAD 16 3807912 3807912 + Silent SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr16:3807912G>A c.3507C>T c.(3505-3507)cgC>cgT p.R1169R COADREAD 16 3807914 3807914 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr16:3807914G>A c.3505C>T c.(3505-3507)Cgc>Tgc p.R1169C COADREAD 16 3807926 3807926 + Missense_Mutation SNP A A G TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:3807926A>G c.3493T>C c.(3493-3495)Tgg>Cgg p.W1165R COADREAD 16 3808046 3808046 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:3808046A>G c.3373T>C c.(3373-3375)Tat>Cat p.Y1125H COADREAD 16 3808863 3808863 + Nonsense_Mutation SNP C C A TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr16:3808863C>A c.3361G>T c.(3361-3363)Gga>Tga p.G1121* COADREAD 16 3808955 3808955 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3808955A>G c.3269T>C c.(3268-3270)tTa>tCa p.L1090S COADREAD 16 3808956 3808956 + Silent SNP A A G TCGA-A6-6649-01A-11D-1771-10 TCGA-A6-6649-10A-01D-1771-10 g.chr16:3808956A>G c.3268T>C c.(3268-3270)Tta>Cta p.L1090L COADREAD 16 3817735 3817735 + Missense_Mutation SNP T T C TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:3817735T>C c.3236A>G c.(3235-3237)cAg>cGg p.Q1079R COADREAD 16 3817735 3817735 + Missense_Mutation SNP T T C TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr16:3817735T>C c.3236A>G c.(3235-3237)cAg>cGg p.Q1079R COADREAD 16 3817812 3817812 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:3817812A>G c.3159T>C c.(3157-3159)ccT>ccC p.P1053P COADREAD 16 3817813 3817813 + Missense_Mutation SNP G G T TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr16:3817813G>T c.3158C>A c.(3157-3159)cCt>cAt p.P1053H COADREAD 16 3819176 3819176 + Splice_Site SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr16:3819176T>C c.3059A>G c.(3058-3060)gAg>gGg p.E1020G COADREAD 16 3820640 3820640 + Silent SNP C C T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:3820640C>T c.2811G>A c.(2809-2811)ccG>ccA p.P937P COADREAD 16 3820703 3820703 + Silent SNP A A G TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3820703A>G c.2748T>C c.(2746-2748)ccT>ccC p.P916P COADREAD 16 3820773 3820773 + Missense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:3820773G>A c.2678C>T c.(2677-2679)tCg>tTg p.S893L COADREAD 16 3820774 3820774 + Missense_Mutation SNP A A G TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr16:3820774A>G c.2677T>C c.(2677-2679)Tcg>Ccg p.S893P COADREAD 16 3820774 3820774 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:3820774A>G c.2677T>C c.(2677-2679)Tcg>Ccg p.S893P COADREAD 16 3820934 3820934 + Missense_Mutation SNP C C A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr16:3820934C>A c.2517G>T c.(2515-2517)caG>caT p.Q839H COADREAD 16 3820935 3820935 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr16:3820935T>C c.2516A>G c.(2515-2517)cAg>cGg p.Q839R COADREAD 16 3823907 3823907 + Missense_Mutation SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr16:3823907G>A c.2308C>T c.(2308-2310)Cct>Tct p.P770S COADREAD 16 3824575 3824575 + Missense_Mutation SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr16:3824575G>A c.2278C>T c.(2278-2280)Cca>Tca p.P760S COADREAD 16 3824598 3824598 + Missense_Mutation SNP T T C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr16:3824598T>C c.2255A>G c.(2254-2256)cAg>cGg p.Q752R COADREAD 16 3824675 3824675 + Silent SNP G G A TCGA-AA-3695-01A-01W-0900-09 TCGA-AA-3695-10A-01W-0900-09 g.chr16:3824675G>A c.2178C>T c.(2176-2178)ccC>ccT p.P726P COADREAD 16 3824694 3824694 + Splice_Site SNP C C A TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr16:3824694C>A c.2159G>T c.(2158-2160)gGg>gTg p.G720V COADREAD 16 3828111 3828111 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3828111G>A c.2014C>T c.(2014-2016)Cgt>Tgt p.R672C COADREAD 16 3828175 3828175 + Nonsense_Mutation SNP A A C TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3828175A>C c.1950T>G c.(1948-1950)taT>taG p.Y650* COADREAD 16 3828184 3828184 + Splice_Site SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr16:3828184C>A c.e10-1 COADREAD 16 3830755 3830755 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr16:3830755G>A c.1801C>T c.(1801-1803)Cgg>Tgg p.R601W COADREAD 16 3832829 3832829 + Missense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr16:3832829C>T c.1429G>A c.(1429-1431)Gac>Aac p.D477N COADREAD 16 3832857 3832857 + Silent SNP G G T TCGA-DM-A28C-01A-11D-A16V-10 TCGA-DM-A28C-10A-01D-A16V-10 g.chr16:3832857G>T c.1401C>A c.(1399-1401)gcC>gcA p.A467A COADREAD 16 3832858 3832858 + Missense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr16:3832858G>A c.1400C>T c.(1399-1401)gCc>gTc p.A467V COADREAD 16 3841993 3841993 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3841993C>T c.1319G>A c.(1318-1320)cGa>cAa p.R440Q COADREAD 16 3900336 3900336 + Missense_Mutation SNP C C T TCGA-AD-6963-01A-11D-1924-10 TCGA-AD-6963-10A-01D-1924-10 g.chr16:3900336C>T c.760G>A c.(760-762)Gcg>Acg p.A254T COADREAD 16 3900430 3900430 + Silent SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr16:3900430A>G c.666T>C c.(664-666)gcT>gcC p.A222A COADREAD 16 3900435 3900435 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr16:3900435C>T c.661G>A c.(661-663)Gga>Aga p.G221R COADREAD 16 3900630 3900630 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:3900630G>T c.466C>A c.(466-468)Caa>Aaa p.Q156K COADREAD 16 3900697 3900697 + Silent SNP C C G TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr16:3900697C>G c.399G>C c.(397-399)ctG>ctC p.L133L COADREAD 16 3900740 3900740 + Missense_Mutation SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:3900740C>A c.356G>T c.(355-357)gGc>gTc p.G119V COADREAD 16 3900775 3900775 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3900775C>T c.321G>A c.(319-321)ccG>ccA p.P107P COADREAD 16 3900826 3900826 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3900826G>A c.270C>T c.(268-270)agC>agT p.S90S COADREAD 16 3900860 3900860 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3900860C>A c.236G>T c.(235-237)gGc>gTc p.G79V COADREAD 16 3900872 3900872 + Missense_Mutation SNP C C A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3900872C>A c.224G>T c.(223-225)cGa>cTa p.R75L DLBC 16 3781324 3781326 + In_Frame_Del DEL AGG AGG - TCGA-GS-A9TX-01A-11D-A382-10 TCGA-GS-A9TX-10A-01D-A385-10 g.chr16:3781324_3781326delAGG c.5039_5041delCCT c.(5038-5043)tccttg>ttg p.S1680del DLBC 16 3786764 3786764 + Missense_Mutation SNP T T A TCGA-GR-A4D4-01A-11D-A31X-10 TCGA-GR-A4D4-10A-01D-A31X-10 g.chr16:3786764T>A c.4447A>T c.(4447-4449)Atc>Ttc p.I1483F DLBC 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C DLBC 16 3789597 3789597 + Missense_Mutation SNP C C A TCGA-GR-A4D9-01B-11D-A31X-10 TCGA-GR-A4D9-10A-01D-A31X-10 g.chr16:3789597C>A c.4262G>T c.(4261-4263)tGc>tTc p.C1421F DLBC 16 3808872 3808872 + Nonsense_Mutation SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr16:3808872G>A c.3352C>T c.(3352-3354)Cag>Tag p.Q1118* DLBC 16 3828721 3828721 + Missense_Mutation SNP A A G TCGA-FA-A7Q1-01A-11D-A382-10 TCGA-FA-A7Q1-10A-01D-A385-10 g.chr16:3828721A>G c.1921T>C c.(1921-1923)Tac>Cac p.Y641H ESCA 16 3778029 3778029 + Missense_Mutation SNP C C T TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr16:3778029C>T c.7019G>A c.(7018-7020)aGt>aAt p.S2340N ESCA 16 3778125 3778125 + Frame_Shift_Del DEL G G - TCGA-R6-A6Y2-01B-11D-A33E-09 TCGA-R6-A6Y2-10A-01D-A33H-09 g.chr16:3778125delG c.6923delC c.(6922-6924)ccafs p.P2308fs ESCA 16 3781439 3781439 + Silent SNP G G A TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chr16:3781439G>A c.4926C>T c.(4924-4926)gtC>gtT p.V1642V ESCA 16 3786138 3786138 + Missense_Mutation SNP C C G TCGA-L5-A43H-01A-11D-A247-09 TCGA-L5-A43H-11A-11D-A247-09 g.chr16:3786138C>G c.4627G>C c.(4627-4629)Gat>Cat p.D1543H ESCA 16 3788617 3788617 + Missense_Mutation SNP C C A TCGA-VR-AA7D-01A-11D-A403-09 TCGA-VR-AA7D-10A-01D-A403-09 g.chr16:3788617C>A c.4337G>T c.(4336-4338)cGc>cTc p.R1446L ESCA 16 3789596 3789596 + Nonsense_Mutation SNP G G T TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr16:3789596G>T c.4263C>A c.(4261-4263)tgC>tgA p.C1421* ESCA 16 3807902 3807902 + Nonsense_Mutation SNP G G A TCGA-LN-A49K-01A-11D-A247-09 TCGA-LN-A49K-10A-01D-A247-09 g.chr16:3807902G>A c.3517C>T c.(3517-3519)Cga>Tga p.R1173* ESCA 16 3820588 3820588 + Nonsense_Mutation SNP G G A TCGA-JY-A6FE-01A-11D-A33E-09 TCGA-JY-A6FE-10A-01D-A33H-09 g.chr16:3820588G>A c.2863C>T c.(2863-2865)Cag>Tag p.Q955* ESCA 16 3820633 3820633 + Missense_Mutation SNP C C A TCGA-LN-A49W-01A-11D-A27G-09 TCGA-LN-A49W-10A-01D-A27G-09 g.chr16:3820633C>A c.2818G>T c.(2818-2820)Gct>Tct p.A940S ESCA 16 3820668 3820668 + Missense_Mutation SNP G G T TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr16:3820668G>T c.2783C>A c.(2782-2784)cCg>cAg p.P928Q ESCA 16 3824652 3824652 + Nonsense_Mutation SNP A A T TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr16:3824652A>T c.2201T>A c.(2200-2202)tTg>tAg p.L734* ESCA 16 3828084 3828085 + Frame_Shift_Ins INS - - C TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr16:3828084_3828085insC c.2040_2041insG c.(2038-2043)gggaacfs p.N681fs ESCA 16 3843431 3843431 + Missense_Mutation SNP A A G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr16:3843431A>G c.1172T>C c.(1171-1173)gTt>gCt p.V391A ESCA 16 3900661 3900661 + Frame_Shift_Del DEL G G - TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr16:3900661delG c.435delC c.(433-435)cccfs p.P145fs GBM 16 3779062 3779062 + Missense_Mutation SNP C C T TCGA-28-2514-01A-02D-1494-08 TCGA-28-2514-10A-01D-1494-08 g.chr16:3779062C>T c.5986G>A c.(5986-5988)Gcc>Acc p.A1996T GBM 16 3807844 3807844 + Missense_Mutation SNP A A G TCGA-06-0154-01A-03D-1491-08 TCGA-06-0154-10A-01D-1491-08 g.chr16:3807844A>G c.3575T>C c.(3574-3576)gTc>gCc p.V1192A GBM 16 3842056 3842056 + Nonsense_Mutation SNP C C T TCGA-06-0749-01A-01W-0348-08 TCGA-06-0749-10A-01W-0348-08 g.chr16:3842056C>T c.1256G>A c.(1255-1257)tGg>tAg p.W419* GBM 16 3843446 3843446 + Frame_Shift_Del DEL C C - TCGA-02-0047-01A-01D-1490-08 TCGA-02-0047-10A-01D-1490-08 g.chr16:3843446delC c.1157delG c.(1156-1158)cgafs p.R386fs GBMLGG 16 3779062 3779062 + Missense_Mutation SNP C C T TCGA-28-2514-01A-02D-1494-08 TCGA-28-2514-10A-01D-1494-08 g.chr16:3779062C>T c.5986G>A c.(5986-5988)Gcc>Acc p.A1996T GBMLGG 16 3781317 3781317 + Missense_Mutation SNP C C G TCGA-DU-6405-01A-11D-1705-08 TCGA-DU-6405-10A-01D-1705-08 g.chr16:3781317C>G c.5048G>C c.(5047-5049)cGc>cCc p.R1683P GBMLGG 16 3781375 3781375 + Missense_Mutation SNP G G A TCGA-HT-8110-01A-11D-2395-08 TCGA-HT-8110-10A-01D-2396-08 g.chr16:3781375G>A c.4990C>T c.(4990-4992)Cgc>Tgc p.R1664C GBMLGG 16 3781930 3781930 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3781930C>A c.4737G>T c.(4735-4737)caG>caT p.Q1579H GBMLGG 16 3786041 3786041 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3786041G>T c.4724C>A c.(4723-4725)aCt>aAt p.T1575N GBMLGG 16 3807844 3807844 + Missense_Mutation SNP A A G TCGA-06-0154-01A-03D-1491-08 TCGA-06-0154-10A-01D-1491-08 g.chr16:3807844A>G c.3575T>C c.(3574-3576)gTc>gCc p.V1192A GBMLGG 16 3817888 3817888 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3817888C>T c.3083G>A c.(3082-3084)gGa>gAa p.G1028E GBMLGG 16 3828795 3828795 + Frame_Shift_Del DEL G G - TCGA-HT-8011-01A-11D-2395-08 TCGA-HT-8011-10A-01D-2396-08 g.chr16:3828795delG c.1847delC c.(1846-1848)cctfs p.P616fs GBMLGG 16 3832889 3832889 + Missense_Mutation SNP T T C TCGA-DH-A66F-01A-11D-A29Q-08 TCGA-DH-A66F-10A-01D-A29Q-08 g.chr16:3832889T>C c.1369A>G c.(1369-1371)Att>Gtt p.I457V GBMLGG 16 3842056 3842056 + Nonsense_Mutation SNP C C T TCGA-06-0749-01A-01W-0348-08 TCGA-06-0749-10A-01W-0348-08 g.chr16:3842056C>T c.1256G>A c.(1255-1257)tGg>tAg p.W419* GBMLGG 16 3843446 3843446 + Frame_Shift_Del DEL C C - TCGA-02-0047-01A-01D-1490-08 TCGA-02-0047-10A-01D-1490-08 g.chr16:3843446delC c.1157delG c.(1156-1158)cgafs p.R386fs GBMLGG 16 3843551 3843551 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3843551C>T c.1052G>A c.(1051-1053)cGc>cAc p.R351H GBMLGG 16 3929833 3929833 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3929833C>A c.85G>T c.(85-87)Gat>Tat p.D29Y HNSC 16 3777767 3777767 + Silent SNP G G A TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr16:3777767G>A c.7281C>T c.(7279-7281)gtC>gtT p.V2427V HNSC 16 3778359 3778359 + Missense_Mutation SNP T T A TCGA-CV-6951-01A-11D-1912-08 TCGA-CV-6951-10A-01D-1912-08 g.chr16:3778359T>A c.6689A>T c.(6688-6690)cAg>cTg p.Q2230L HNSC 16 3778856 3778856 + Silent SNP G G A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr16:3778856G>A c.6192C>T c.(6190-6192)ccC>ccT p.P2064P HNSC 16 3778902 3778902 + Missense_Mutation SNP G G T TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr16:3778902G>T c.6146C>A c.(6145-6147)gCt>gAt p.A2049D HNSC 16 3779048 3779048 + Silent SNP C C T TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr16:3779048C>T c.6000G>A c.(5998-6000)ctG>ctA p.L2000L HNSC 16 3779447 3779447 + Silent SNP C C T TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chr16:3779447C>T c.5601G>A c.(5599-5601)cgG>cgA p.R1867R HNSC 16 3779591 3779591 + Nonsense_Mutation SNP G G T TCGA-CV-7429-01A-11D-2129-08 TCGA-CV-7429-10A-01D-2129-08 g.chr16:3779591G>T c.5457C>A c.(5455-5457)tgC>tgA p.C1819* HNSC 16 3779596 3779596 + Missense_Mutation SNP C C A TCGA-UF-A7JJ-01A-11D-A34J-08 TCGA-UF-A7JJ-10A-01D-A34M-08 g.chr16:3779596C>A c.5452G>T c.(5452-5454)Gtg>Ttg p.V1818L HNSC 16 3779766 3779766 + Nonsense_Mutation SNP G G C TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr16:3779766G>C c.5282C>G c.(5281-5283)tCa>tGa p.S1761* HNSC 16 3781253 3781253 + Silent SNP G G C TCGA-CR-6471-01A-11D-1870-08 TCGA-CR-6471-10A-01D-1870-08 g.chr16:3781253G>C c.5112C>G c.(5110-5112)gtC>gtG p.V1704V HNSC 16 3781357 3781357 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr16:3781357G>A c.5008C>T c.(5008-5010)Ctc>Ttc p.L1670F HNSC 16 3781358 3781358 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr16:3781358G>A c.5007C>T c.(5005-5007)acC>acT p.T1669T HNSC 16 3781465 3781465 + Missense_Mutation SNP C C A TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr16:3781465C>A c.4900G>T c.(4900-4902)Gtg>Ttg p.V1634L HNSC 16 3781794 3781794 + Missense_Mutation SNP T T C TCGA-CQ-A4CI-01A-11D-A25Y-08 TCGA-CQ-A4CI-10A-01D-A25Y-08 g.chr16:3781794T>C c.4873A>G c.(4873-4875)Atg>Gtg p.M1625V HNSC 16 3781826 3781826 + Missense_Mutation SNP G G A TCGA-CV-5432-01A-02D-1683-08 TCGA-CV-5432-10A-01D-1870-08 g.chr16:3781826G>A c.4841C>T c.(4840-4842)tCc>tTc p.S1614F HNSC 16 3786099 3786099 + Missense_Mutation SNP G G C TCGA-BA-4074-01A-01D-1434-08 TCGA-BA-4074-10A-01D-1434-08 g.chr16:3786099G>C c.4666C>G c.(4666-4668)Cta>Gta p.L1556V HNSC 16 3786674 3786674 + Missense_Mutation SNP C C T TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr16:3786674C>T c.4537G>A c.(4537-4539)Gag>Aag p.E1513K HNSC 16 3786770 3786770 + Missense_Mutation SNP C C T TCGA-CR-6478-01A-11D-1870-08 TCGA-CR-6478-10A-01D-1870-08 g.chr16:3786770C>T c.4441G>A c.(4441-4443)Gat>Aat p.D1481N HNSC 16 3786795 3786795 + Missense_Mutation SNP C C A TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr16:3786795C>A c.4416G>T c.(4414-4416)tgG>tgT p.W1472C HNSC 16 3788605 3788605 + Missense_Mutation SNP T T C TCGA-CV-6962-01A-11D-1912-08 TCGA-CV-6962-10A-01D-1912-08 g.chr16:3788605T>C c.4349A>G c.(4348-4350)tAc>tGc p.Y1450C HNSC 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C HNSC 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C HNSC 16 3788645 3788646 + Missense_Mutation DNP TA TA AC TCGA-CV-7434-01A-11D-2129-08 TCGA-CV-7434-10A-01D-2129-08 g.chr16:3788645_3788646TA>AC c.4308_4309TA>GT c.(4306-4311)agTAtt>agGTtt p.1436_1437SI>RF HNSC 16 3788663 3788663 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:3788663T>C c.4291A>G c.(4291-4293)Att>Gtt p.I1431V HNSC 16 3789597 3789597 + Missense_Mutation SNP C C A TCGA-QK-A6IJ-01A-11D-A31L-08 TCGA-QK-A6IJ-10A-01D-A31J-08 g.chr16:3789597C>A c.4262G>T c.(4261-4263)tGc>tTc p.C1421F HNSC 16 3789610 3789610 + Missense_Mutation SNP A A G TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr16:3789610A>G c.4249T>C c.(4249-4251)Tac>Cac p.Y1417H HNSC 16 3789616 3789616 + Nonsense_Mutation SNP G G A TCGA-UF-A7JA-01A-12D-A34J-08 TCGA-UF-A7JA-10A-01D-A34M-08 g.chr16:3789616G>A c.4243C>T c.(4243-4245)Caa>Taa p.Q1415* HNSC 16 3790493 3790493 + Missense_Mutation SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr16:3790493C>T c.4040G>A c.(4039-4041)cGg>cAg p.R1347Q HNSC 16 3790495 3790496 + Frame_Shift_Ins INS - - A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:3790495_3790496insA c.4037_4038insT c.(4036-4038)ttgfs p.L1346fs HNSC 16 3801777 3801777 + Missense_Mutation SNP C C G TCGA-DQ-7592-01A-11D-2078-08 TCGA-DQ-7592-10A-01D-2078-08 g.chr16:3801777C>G c.3729G>C c.(3727-3729)gaG>gaC p.E1243D HNSC 16 3817904 3817904 + Missense_Mutation SNP C C T TCGA-CN-4736-01A-01D-1434-08 TCGA-CN-4736-10A-01D-1434-08 g.chr16:3817904C>T c.3067G>A c.(3067-3069)Gag>Aag p.E1023K HNSC 16 3819189 3819189 + Nonsense_Mutation SNP C C A TCGA-CQ-5333-01A-01D-2394-08 TCGA-CQ-5333-10A-01D-2394-08 g.chr16:3819189C>A c.3046G>T c.(3046-3048)Gag>Tag p.E1016* HNSC 16 3819250 3819250 + Silent SNP C C T TCGA-CV-A6JE-01A-11D-A31L-08 TCGA-CV-A6JE-10A-01D-A31J-08 g.chr16:3819250C>T c.2985G>A c.(2983-2985)ctG>ctA p.L995L HNSC 16 3820572 3820572 + Splice_Site SNP G G C TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr16:3820572G>C c.2879C>G c.(2878-2880)cCg>cGg p.P960R HNSC 16 3820641 3820641 + Frame_Shift_Del DEL G G - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:3820641delG c.2810delC c.(2809-2811)ccgfs p.P937fs HNSC 16 3820792 3820792 + Nonsense_Mutation SNP G G A TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr16:3820792G>A c.2659C>T c.(2659-2661)Cag>Tag p.Q887* HNSC 16 3820844 3820844 + Silent SNP G G C TCGA-CN-4740-01A-01D-1434-08 TCGA-CN-4740-10A-01D-1434-08 g.chr16:3820844G>C c.2607C>G c.(2605-2607)ctC>ctG p.L869L HNSC 16 3823862 3823862 + Missense_Mutation SNP C C T TCGA-BB-A5HY-01A-11D-A28R-08 TCGA-BB-A5HY-10A-01D-A28U-08 g.chr16:3823862C>T c.2353G>A c.(2353-2355)Gcc>Acc p.A785T HNSC 16 3828020 3828020 + Missense_Mutation SNP C C G TCGA-IQ-7631-01A-11D-2078-08 TCGA-IQ-7631-10A-01D-2078-08 g.chr16:3828020C>G c.2105G>C c.(2104-2106)aGa>aCa p.R702T HNSC 16 3828790 3828790 + Missense_Mutation SNP G G T TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr16:3828790G>T c.1852C>A c.(1852-1854)Ccc>Acc p.P618T HNSC 16 3830807 3830809 + In_Frame_Del DEL AGG AGG - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:3830807_3830809delAGG c.1747_1749delCCT c.(1747-1749)cctdel p.P583del HNSC 16 3830809 3830809 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr16:3830809G>A c.1747C>T c.(1747-1749)Cct>Tct p.P583S HNSC 16 3843540 3843541 + Frame_Shift_Ins INS - - T TCGA-BA-A6D8-01A-31D-A31L-08 TCGA-BA-A6D8-10A-01D-A31J-08 g.chr16:3843540_3843541insT c.1062_1063insA c.(1060-1065)atacagfs p.Q355fs HNSC 16 3900396 3900396 + Missense_Mutation SNP C C G TCGA-CN-6988-01A-11D-1912-08 TCGA-CN-6988-10A-01D-1912-08 g.chr16:3900396C>G c.700G>C c.(700-702)Gcc>Ccc p.A234P HNSC 16 3900762 3900762 + Missense_Mutation SNP T T C TCGA-CV-A6JE-01A-11D-A31L-08 TCGA-CV-A6JE-10A-01D-A31J-08 g.chr16:3900762T>C c.334A>G c.(334-336)Atg>Gtg p.M112V HNSC 16 3900963 3900963 + Missense_Mutation SNP T T C TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chr16:3900963T>C c.133A>G c.(133-135)Ata>Gta p.I45V KICH 16 3817815 3817815 + Silent SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr16:3817815T>C c.3156A>G c.(3154-3156)aaA>aaG p.K1052K KIPAN 16 3778974 3778974 + Missense_Mutation SNP G G T TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr16:3778974G>T c.6074C>A c.(6073-6075)cCc>cAc p.P2025H KIPAN 16 3779018 3779018 + Silent SNP C C T TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr16:3779018C>T c.6030G>A c.(6028-6030)ggG>ggA p.G2010G KIPAN 16 3779274 3779274 + Missense_Mutation SNP G G C TCGA-2Z-A9J6-01A-11D-A382-10 TCGA-2Z-A9J6-10A-01D-A385-10 g.chr16:3779274G>C c.5774C>G c.(5773-5775)gCc>gGc p.A1925G KIPAN 16 3786685 3786685 + Missense_Mutation SNP T T C TCGA-4A-A93Y-01A-11D-A36X-10 TCGA-4A-A93Y-10A-01D-A370-10 g.chr16:3786685T>C c.4526A>G c.(4525-4527)aAg>aGg p.K1509R KIPAN 16 3807365 3807365 + Missense_Mutation SNP G G T TCGA-BP-4331-01A-01D-1366-10 TCGA-BP-4331-11A-01D-1366-10 g.chr16:3807365G>T c.3622C>A c.(3622-3624)Cca>Aca p.P1208T KIPAN 16 3807907 3807907 + Missense_Mutation SNP G G A TCGA-A4-7997-01A-11D-2201-08 TCGA-A4-7997-10A-01D-2201-08 g.chr16:3807907G>A c.3512C>T c.(3511-3513)aCa>aTa p.T1171I KIPAN 16 3808859 3808859 + Missense_Mutation SNP A A G TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr16:3808859A>G c.3365T>C c.(3364-3366)aTt>aCt p.I1122T KIPAN 16 3817815 3817815 + Silent SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr16:3817815T>C c.3156A>G c.(3154-3156)aaA>aaG p.K1052K KIPAN 16 3817823 3817823 + Nonsense_Mutation SNP C C A TCGA-P4-A5EA-01A-11D-A28G-10 TCGA-P4-A5EA-11A-11D-A28G-10 g.chr16:3817823C>A c.3148G>T c.(3148-3150)Gaa>Taa p.E1050* KIPAN 16 3843626 3843626 + Splice_Site SNP G G A TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr16:3843626G>A c.977C>T c.(976-978)tCt>tTt p.S326F KIPAN 16 3860637 3860637 + Silent SNP G G A TCGA-G7-A4TM-01A-11D-A31X-10 TCGA-G7-A4TM-10B-01D-A31X-10 g.chr16:3860637G>A c.942C>T c.(940-942)atC>atT p.I314I KIPAN 16 3860645 3860645 + Missense_Mutation SNP T T C TCGA-MH-A856-01A-11D-A34Z-10 TCGA-MH-A856-10A-01D-A34Z-10 g.chr16:3860645T>C c.934A>G c.(934-936)Aca>Gca p.T312A KIPAN 16 3860701 3860701 + Missense_Mutation SNP A A G TCGA-B0-5706-01A-11D-1534-10 TCGA-B0-5706-11A-01D-1534-10 g.chr16:3860701A>G c.878T>C c.(877-879)gTg>gCg p.V293A KIPAN 16 3901001 3901001 + Missense_Mutation SNP G G A TCGA-HE-A5NJ-01A-11D-A26P-10 TCGA-HE-A5NJ-10A-01D-A26P-10 g.chr16:3901001G>A c.95C>T c.(94-96)tCa>tTa p.S32L KIRC 16 3807365 3807365 + Missense_Mutation SNP G G T TCGA-BP-4331-01A-01D-1366-10 TCGA-BP-4331-11A-01D-1366-10 g.chr16:3807365G>T c.3622C>A c.(3622-3624)Cca>Aca p.P1208T KIRC 16 3843626 3843626 + Splice_Site SNP G G A TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr16:3843626G>A c.977C>T c.(976-978)tCt>tTt p.S326F KIRC 16 3860701 3860701 + Missense_Mutation SNP A A G TCGA-B0-5706-01A-11D-1534-10 TCGA-B0-5706-11A-01D-1534-10 g.chr16:3860701A>G c.878T>C c.(877-879)gTg>gCg p.V293A KIRP 16 3778974 3778974 + Missense_Mutation SNP G G T TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr16:3778974G>T c.6074C>A c.(6073-6075)cCc>cAc p.P2025H KIRP 16 3779018 3779018 + Silent SNP C C T TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr16:3779018C>T c.6030G>A c.(6028-6030)ggG>ggA p.G2010G KIRP 16 3779274 3779274 + Missense_Mutation SNP G G C TCGA-2Z-A9J6-01A-11D-A382-10 TCGA-2Z-A9J6-10A-01D-A385-10 g.chr16:3779274G>C c.5774C>G c.(5773-5775)gCc>gGc p.A1925G KIRP 16 3786685 3786685 + Missense_Mutation SNP T T C TCGA-4A-A93Y-01A-11D-A36X-10 TCGA-4A-A93Y-10A-01D-A370-10 g.chr16:3786685T>C c.4526A>G c.(4525-4527)aAg>aGg p.K1509R KIRP 16 3807907 3807907 + Missense_Mutation SNP G G A TCGA-A4-7997-01A-11D-2201-08 TCGA-A4-7997-10A-01D-2201-08 g.chr16:3807907G>A c.3512C>T c.(3511-3513)aCa>aTa p.T1171I KIRP 16 3808859 3808859 + Missense_Mutation SNP A A G TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr16:3808859A>G c.3365T>C c.(3364-3366)aTt>aCt p.I1122T KIRP 16 3817823 3817823 + Nonsense_Mutation SNP C C A TCGA-P4-A5EA-01A-11D-A28G-10 TCGA-P4-A5EA-11A-11D-A28G-10 g.chr16:3817823C>A c.3148G>T c.(3148-3150)Gaa>Taa p.E1050* KIRP 16 3860637 3860637 + Silent SNP G G A TCGA-G7-A4TM-01A-11D-A31X-10 TCGA-G7-A4TM-10B-01D-A31X-10 g.chr16:3860637G>A c.942C>T c.(940-942)atC>atT p.I314I KIRP 16 3860645 3860645 + Missense_Mutation SNP T T C TCGA-MH-A856-01A-11D-A34Z-10 TCGA-MH-A856-10A-01D-A34Z-10 g.chr16:3860645T>C c.934A>G c.(934-936)Aca>Gca p.T312A KIRP 16 3901001 3901001 + Missense_Mutation SNP G G A TCGA-HE-A5NJ-01A-11D-A26P-10 TCGA-HE-A5NJ-10A-01D-A26P-10 g.chr16:3901001G>A c.95C>T c.(94-96)tCa>tTa p.S32L LGG 16 3781317 3781317 + Missense_Mutation SNP C C G TCGA-DU-6405-01A-11D-1705-08 TCGA-DU-6405-10A-01D-1705-08 g.chr16:3781317C>G c.5048G>C c.(5047-5049)cGc>cCc p.R1683P LGG 16 3781375 3781375 + Missense_Mutation SNP G G A TCGA-HT-8110-01A-11D-2395-08 TCGA-HT-8110-10A-01D-2396-08 g.chr16:3781375G>A c.4990C>T c.(4990-4992)Cgc>Tgc p.R1664C LGG 16 3781930 3781930 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3781930C>A c.4737G>T c.(4735-4737)caG>caT p.Q1579H LGG 16 3786041 3786041 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3786041G>T c.4724C>A c.(4723-4725)aCt>aAt p.T1575N LGG 16 3817888 3817888 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3817888C>T c.3083G>A c.(3082-3084)gGa>gAa p.G1028E LGG 16 3828795 3828795 + Frame_Shift_Del DEL G G - TCGA-HT-8011-01A-11D-2395-08 TCGA-HT-8011-10A-01D-2396-08 g.chr16:3828795delG c.1847delC c.(1846-1848)cctfs p.P616fs LGG 16 3832889 3832889 + Missense_Mutation SNP T T C TCGA-DH-A66F-01A-11D-A29Q-08 TCGA-DH-A66F-10A-01D-A29Q-08 g.chr16:3832889T>C c.1369A>G c.(1369-1371)Att>Gtt p.I457V LGG 16 3843551 3843551 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3843551C>T c.1052G>A c.(1051-1053)cGc>cAc p.R351H LGG 16 3929833 3929833 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3929833C>A c.85G>T c.(85-87)Gat>Tat p.D29Y LIHC 16 3777763 3777763 + Frame_Shift_Del DEL C C - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr16:3777763delC c.7285delG c.(7285-7287)gacfs p.D2429fs LIHC 16 3778015 3778015 + Missense_Mutation SNP A A G TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr16:3778015A>G c.7033T>C c.(7033-7035)Tct>Cct p.S2345P LIHC 16 3778391 3778391 + Silent SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr16:3778391G>T c.6657C>A c.(6655-6657)gcC>gcA p.A2219A LIHC 16 3778436 3778436 + Silent SNP C C T TCGA-WQ-A9G7-01A-11D-A36X-10 TCGA-WQ-A9G7-10A-01D-A370-10 g.chr16:3778436C>T c.6612G>A c.(6610-6612)caG>caA p.Q2204Q LIHC 16 3778620 3778620 + Missense_Mutation SNP T T C TCGA-DD-A1EA-01A-11D-A12Z-10 TCGA-DD-A1EA-10A-01D-A12Z-10 g.chr16:3778620T>C c.6428A>G c.(6427-6429)aAt>aGt p.N2143S LIHC 16 3788625 3788625 + Silent SNP A A G TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr16:3788625A>G c.4329T>C c.(4327-4329)cgT>cgC p.R1443R LIHC 16 3799678 3799678 + Silent SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr16:3799678A>G c.3786T>C c.(3784-3786)atT>atC p.I1262I LIHC 16 3807812 3807812 + Nonsense_Mutation SNP T T A TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr16:3807812T>A c.3607A>T c.(3607-3609)Aag>Tag p.K1203* LIHC 16 3830772 3830772 + Missense_Mutation SNP T T C TCGA-G3-A7M7-01A-12D-A34Z-10 TCGA-G3-A7M7-10A-01D-A34Z-10 g.chr16:3830772T>C c.1784A>G c.(1783-1785)cAt>cGt p.H595R LIHC 16 3843532 3843532 + Silent SNP C C T TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr16:3843532C>T c.1071G>A c.(1069-1071)caG>caA p.Q357Q LIHC 16 3860606 3860606 + Missense_Mutation SNP T T A TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr16:3860606T>A c.973A>T c.(973-975)Atg>Ttg p.M325L LUAD 16 3777847 3777847 + Missense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr16:3777847C>A c.7201G>T c.(7201-7203)Ggg>Tgg p.G2401W LUAD 16 3777990 3777990 + Missense_Mutation SNP C C A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr16:3777990C>A c.7058G>T c.(7057-7059)cGg>cTg p.R2353L LUAD 16 3778085 3778085 + Silent SNP G G C TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr16:3778085G>C c.6963C>G c.(6961-6963)ctC>ctG p.L2321L LUAD 16 3778145 3778145 + Missense_Mutation SNP C C T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr16:3778145C>T c.6903G>A c.(6901-6903)atG>atA p.M2301I LUAD 16 3778569 3778569 + Missense_Mutation SNP G G A TCGA-17-Z059-01A-01W-0747-08 TCGA-17-Z059-11A-01W-0747-08 g.chr16:3778569G>A c.6479C>T c.(6478-6480)gCg>gTg p.A2160V LUAD 16 3778778 3778778 + Silent SNP G G C TCGA-17-Z053-01A-01W-0747-08 TCGA-17-Z053-11A-01W-0747-08 g.chr16:3778778G>C c.6270C>G c.(6268-6270)ctC>ctG p.L2090L LUAD 16 3778918 3778918 + Missense_Mutation SNP C C A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr16:3778918C>A c.6130G>T c.(6130-6132)Gcc>Tcc p.A2044S LUAD 16 3778942 3778942 + Missense_Mutation SNP G G C TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr16:3778942G>C c.6106C>G c.(6106-6108)Ccc>Gcc p.P2036A LUAD 16 3779424 3779424 + Missense_Mutation SNP C C A TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr16:3779424C>A c.5624G>T c.(5623-5625)cGc>cTc p.R1875L LUAD 16 3779779 3779779 + Missense_Mutation SNP C C A TCGA-99-8033-01A-11D-2238-08 TCGA-99-8033-10A-01D-2238-08 g.chr16:3779779C>A c.5269G>T c.(5269-5271)Ggc>Tgc p.G1757C LUAD 16 3779782 3779782 + Nonsense_Mutation SNP G G A TCGA-05-4426-01A-01D-1265-08 TCGA-05-4426-10A-01D-1265-08 g.chr16:3779782G>A c.5266C>T c.(5266-5268)Cag>Tag p.Q1756* LUAD 16 3781195 3781195 + Missense_Mutation SNP C C T TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr16:3781195C>T c.5170G>A c.(5170-5172)Gag>Aag p.E1724K LUAD 16 3781236 3781236 + Missense_Mutation SNP C C G TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr16:3781236C>G c.5129G>C c.(5128-5130)tGc>tCc p.C1710S LUAD 16 3781862 3781862 + Missense_Mutation SNP C C A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr16:3781862C>A c.4805G>T c.(4804-4806)cGc>cTc p.R1602L LUAD 16 3781863 3781863 + Missense_Mutation SNP G G A TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr16:3781863G>A c.4804C>T c.(4804-4806)Cgc>Tgc p.R1602C LUAD 16 3786117 3786117 + Missense_Mutation SNP C C T TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr16:3786117C>T c.4648G>A c.(4648-4650)Gaa>Aaa p.E1550K LUAD 16 3786795 3786795 + Missense_Mutation SNP C C A TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr16:3786795C>A c.4416G>T c.(4414-4416)tgG>tgT p.W1472C LUAD 16 3789613 3789613 + Missense_Mutation SNP C C G TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr16:3789613C>G c.4246G>C c.(4246-4248)Gaa>Caa p.E1416Q LUAD 16 3790432 3790432 + Missense_Mutation SNP C C G TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr16:3790432C>G c.4101G>C c.(4099-4101)aaG>aaC p.K1367N LUAD 16 3795338 3795338 + Missense_Mutation SNP T T C TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr16:3795338T>C c.3854A>G c.(3853-3855)gAg>gGg p.E1285G LUAD 16 3801726 3801726 + Splice_Site SNP C C A TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr16:3801726C>A c.e20+1 LUAD 16 3807317 3807317 + Missense_Mutation SNP C C A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr16:3807317C>A c.3670G>T c.(3670-3672)Gat>Tat p.D1224Y LUAD 16 3817765 3817765 + Missense_Mutation SNP C C T TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr16:3817765C>T c.3206G>A c.(3205-3207)gGc>gAc p.G1069D LUAD 16 3817811 3817811 + Missense_Mutation SNP C C T TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr16:3817811C>T c.3160G>A c.(3160-3162)Gaa>Aaa p.E1054K LUAD 16 3831292 3831292 + Missense_Mutation SNP T T A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr16:3831292T>A c.1589A>T c.(1588-1590)aAc>aTc p.N530I LUAD 16 3843416 3843416 + Missense_Mutation SNP G G C TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr16:3843416G>C c.1187C>G c.(1186-1188)aCg>aGg p.T396R LUAD 16 3843558 3843558 + Nonsense_Mutation SNP C C A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr16:3843558C>A c.1045G>T c.(1045-1047)Gaa>Taa p.E349* LUAD 16 3860676 3860676 + Missense_Mutation SNP C C A TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr16:3860676C>A c.903G>T c.(901-903)caG>caT p.Q301H LUAD 16 3860755 3860755 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr16:3860755G>T c.824C>A c.(823-825)cCa>cAa p.P275Q LUAD 16 3900443 3900443 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr16:3900443C>A c.653G>T c.(652-654)aGa>aTa p.R218I LUAD 16 3900576 3900576 + Missense_Mutation SNP C C G TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr16:3900576C>G c.520G>C c.(520-522)Ggt>Cgt p.G174R LUAD 16 3900688 3900688 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr16:3900688C>A c.408G>T c.(406-408)caG>caT p.Q136H LUSC 16 3777896 3777896 + Missense_Mutation SNP G G T TCGA-18-3412-01A-01D-0983-08 TCGA-18-3412-11A-01D-0983-08 g.chr16:3777896G>T c.7152C>A c.(7150-7152)caC>caA p.H2384Q LUSC 16 3778059 3778059 + Missense_Mutation SNP A A C TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr16:3778059A>C c.6989T>G c.(6988-6990)cTc>cGc p.L2330R LUSC 16 3778105 3778105 + Missense_Mutation SNP T T A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr16:3778105T>A c.6943A>T c.(6943-6945)Agc>Tgc p.S2315C LUSC 16 3779748 3779748 + Missense_Mutation SNP G G A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr16:3779748G>A c.5300C>T c.(5299-5301)tCa>tTa p.S1767L LUSC 16 3788606 3788606 + Missense_Mutation SNP A A C TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr16:3788606A>C c.4348T>G c.(4348-4350)Tac>Gac p.Y1450D LUSC 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C LUSC 16 3788651 3788651 + Missense_Mutation SNP C C A TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr16:3788651C>A c.4303G>T c.(4303-4305)Gat>Tat p.D1435Y LUSC 16 3789636 3789636 + Missense_Mutation SNP C C T TCGA-18-3407-01A-01D-0983-08 TCGA-18-3407-11A-01D-0983-08 g.chr16:3789636C>T c.4223G>A c.(4222-4224)tGc>tAc p.C1408Y LUSC 16 3795299 3795299 + Missense_Mutation SNP T T C TCGA-21-1081-01A-01D-1521-08 TCGA-21-1081-10B-01D-1521-08 g.chr16:3795299T>C c.3893A>G c.(3892-3894)tAt>tGt p.Y1298C LUSC 16 3808000 3808000 + Missense_Mutation SNP C C T TCGA-18-3408-01A-01D-0983-08 TCGA-18-3408-11A-01D-0983-08 g.chr16:3808000C>T c.3419G>A c.(3418-3420)cGg>cAg p.R1140Q LUSC 16 3820624 3820624 + Nonsense_Mutation SNP G G A TCGA-21-1081-01A-01D-1521-08 TCGA-21-1081-10B-01D-1521-08 g.chr16:3820624G>A c.2827C>T c.(2827-2829)Cag>Tag p.Q943* LUSC 16 3823774 3823774 + Missense_Mutation SNP G G A TCGA-46-6025-01A-11D-1817-08 TCGA-46-6025-10A-01D-1817-08 g.chr16:3823774G>A c.2441C>T c.(2440-2442)cCa>cTa p.P814L LUSC 16 3823884 3823884 + Silent SNP A A G TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chr16:3823884A>G c.2331T>C c.(2329-2331)ggT>ggC p.G777G LUSC 16 3828022 3828022 + Silent SNP C C T TCGA-60-2719-01A-01D-1522-08 TCGA-60-2719-11A-01D-1522-08 g.chr16:3828022C>T c.2103G>A c.(2101-2103)gtG>gtA p.V701V LUSC 16 3828795 3828795 + Missense_Mutation SNP G G C TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr16:3828795G>C c.1847C>G c.(1846-1848)cCt>cGt p.P616R LUSC 16 3830746 3830746 + Silent SNP G G A TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr16:3830746G>A c.1810C>T c.(1810-1812)Cta>Tta p.L604L LUSC 16 3832751 3832751 + Nonsense_Mutation SNP G G A TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr16:3832751G>A c.1507C>T c.(1507-1509)Cag>Tag p.Q503* LUSC 16 3832794 3832794 + Silent SNP G G T TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr16:3832794G>T c.1464C>A c.(1462-1464)ctC>ctA p.L488L LUSC 16 3843455 3843455 + Missense_Mutation SNP G G C TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr16:3843455G>C c.1148C>G c.(1147-1149)cCg>cGg p.P383R LUSC 16 3900414 3900414 + Missense_Mutation SNP T T C TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chr16:3900414T>C c.682A>G c.(682-684)Act>Gct p.T228A LUSC 16 3900926 3900926 + Missense_Mutation SNP C C A TCGA-18-3411-01A-01D-0983-08 TCGA-18-3411-11A-01D-0983-08 g.chr16:3900926C>A c.170G>T c.(169-171)gGg>gTg p.G57V OV 16 3786810 3786810 + Silent SNP C C G TCGA-09-2049-01D-01W-0799-08 TCGA-09-2049-10A-01W-0799-08 g.chr16:3786810C>G c.4401G>C c.(4399-4401)gtG>gtC p.V1467V OV 16 3788596 3788596 + Missense_Mutation SNP A A G TCGA-31-1950-01A-01W-0699-08 TCGA-31-1950-10A-01W-0699-08 g.chr16:3788596A>G c.4358T>C c.(4357-4359)aTc>aCc p.I1453T OV 16 3789578 3789578 + Splice_Site SNP C C A TCGA-29-1703-01A-01W-0633-09 TCGA-29-1703-10A-01W-0633-09 g.chr16:3789578C>A c.e25+1 OV 16 3789724 3789724 + Splice_Site SNP A A C TCGA-04-1338-01A-01W-0484-10 TCGA-04-1338-11A-01W-0485-10 g.chr16:3789724A>C c.4135T>G c.(4135-4137)Ttt>Gtt p.F1379V OV 16 3790512 3790512 + Nonsense_Mutation SNP G G A TCGA-25-1631-01A-01W-0615-10 TCGA-25-1631-10A-01W-0615-10 g.chr16:3790512G>A c.4021C>T c.(4021-4023)Cga>Tga p.R1341* OV 16 3790520 3790520 + Missense_Mutation SNP A A G TCGA-24-0966-01A-01W-0977-09 TCGA-24-0966-10A-01W-0421-09 g.chr16:3790520A>G c.4013T>C c.(4012-4014)tTg>tCg p.L1338S OV 16 3795268 3795281 + Splice_Site DEL AACAACTCACCCTG AACAACTCACCCTG - TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr16:3795268_3795281delAACAACTCACCCTG c.3911_3915delCAGGGTGAGTTGTT c.(3910-3915)tcaggg>t p.SG1304fs OV 16 3819257 3819257 + Frame_Shift_Del DEL G G - TCGA-04-1525-01A-01W-0615-10 TCGA-04-1525-10A-01W-0615-10 g.chr16:3819257delG c.2978delC c.(2977-2979)cctfs p.P993fs OV 16 3820801 3820801 + Missense_Mutation SNP C C T TCGA-04-1350-01A-01W-0490-10 TCGA-04-1350-11A-01W-0490-10 g.chr16:3820801C>T c.2650G>A c.(2650-2652)Gct>Act p.A884T OV 16 3820936 3820942 + Frame_Shift_Del DEL GAGGCCC GAGGCCC - TCGA-13-0724-01A-01W-0372-09 TCGA-13-0724-10B-01W-0372-09 g.chr16:3820936_3820942delGAGGCCC c.2509_2515delGGGCCTC c.(2509-2517)gggcctcagfs p.GPQ837fs OV 16 3843433 3843433 + Missense_Mutation SNP G G C TCGA-29-1705-01A-01W-0633-09 TCGA-29-1705-10A-01W-0633-09 g.chr16:3843433G>C c.1170C>G c.(1168-1170)aaC>aaG p.N390K OV 16 3860721 3860721 + Missense_Mutation SNP C C A TCGA-29-1699-01A-01W-0633-09 TCGA-29-1699-10A-01W-0633-09 g.chr16:3860721C>A c.858G>T c.(856-858)caG>caT p.Q286H PAAD 16 3778862 3778862 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3778862G>A c.6186C>T c.(6184-6186)atC>atT p.I2062I PAAD 16 3801767 3801767 + Missense_Mutation SNP C C T TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr16:3801767C>T c.3739G>A c.(3739-3741)Gag>Aag p.E1247K PAAD 16 3807335 3807335 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3807335G>T c.3652C>A c.(3652-3654)Ctg>Atg p.L1218M PAAD 16 3823809 3823809 + Silent SNP G G A TCGA-YH-A8SY-01A-11D-A377-08 TCGA-YH-A8SY-10A-01D-A37A-08 g.chr16:3823809G>A c.2406C>T c.(2404-2406)tcC>tcT p.S802S PAAD 16 3824628 3824628 + Missense_Mutation SNP C C A TCGA-US-A779-01A-11D-A32N-08 TCGA-US-A779-11A-11D-A32N-08 g.chr16:3824628C>A c.2225G>T c.(2224-2226)cGt>cTt p.R742L PRAD 16 3778253 3778253 + Silent SNP C C T TCGA-CH-5788-01A-11D-1576-08 TCGA-CH-5788-10A-01D-1576-08 g.chr16:3778253C>T c.6795G>A c.(6793-6795)gcG>gcA p.A2265A PRAD 16 3778439 3778451 + Frame_Shift_Del DEL TTGCTGCTGCTGC TTGCTGCTGCTGC - TCGA-EJ-7115-01A-11D-2114-08 TCGA-EJ-7115-10A-01D-2114-08 g.chr16:3778439_3778451delTTGCTGCTGCTGC c.6597_6609delGCAGCAGCAGCAA c.(6595-6609)cagcagcagcagcaafs p.QQQQQ2209fs PRAD 16 3778738 3778738 + Missense_Mutation SNP G G A TCGA-HC-A6AN-01A-11D-A30E-08 TCGA-HC-A6AN-10A-01D-A30H-08 g.chr16:3778738G>A c.6310C>T c.(6310-6312)Cgc>Tgc p.R2104C PRAD 16 3778981 3778981 + Missense_Mutation SNP G G C TCGA-KC-A4BV-01A-31D-A26M-08 TCGA-KC-A4BV-10A-01D-A26K-08 g.chr16:3778981G>C c.6067C>G c.(6067-6069)Cag>Gag p.Q2023E PRAD 16 3779041 3779041 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3779041G>A c.6007C>T c.(6007-6009)Ccc>Tcc p.P2003S PRAD 16 3779687 3779687 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3779687G>A c.5361C>T c.(5359-5361)aaC>aaT p.N1787N PRAD 16 3781218 3781218 + Missense_Mutation SNP G G A TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr16:3781218G>A c.5147C>T c.(5146-5148)aCg>aTg p.T1716M PRAD 16 3786756 3786756 + Silent SNP A A G TCGA-CH-5748-01A-11D-1576-08 TCGA-CH-5748-10A-01D-1576-08 g.chr16:3786756A>G c.4455T>C c.(4453-4455)caT>caC p.H1485H PRAD 16 3807828 3807828 + Silent SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3807828T>C c.3591A>G c.(3589-3591)ggA>ggG p.G1197G PRAD 16 3817735 3817735 + Missense_Mutation SNP T T C TCGA-J4-A83K-01A-11D-A34U-08 TCGA-J4-A83K-10A-01D-A34X-08 g.chr16:3817735T>C c.3236A>G c.(3235-3237)cAg>cGg p.Q1079R PRAD 16 3832871 3832871 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3832871C>A c.1387G>T c.(1387-1389)Ggg>Tgg p.G463W PRAD 16 3842029 3842029 + Missense_Mutation SNP G G T TCGA-CH-5769-01A-11D-1576-08 TCGA-CH-5769-11A-01D-1576-08 g.chr16:3842029G>T c.1283C>A c.(1282-1284)cCt>cAt p.P428H READ 16 3778018 3778018 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3778018G>A c.7030C>T c.(7030-7032)Cgg>Tgg p.R2344W READ 16 3779387 3779387 + Silent SNP T T C TCGA-AF-6672-01A-11D-1826-10 TCGA-AF-6672-10A-01D-1826-10 g.chr16:3779387T>C c.5661A>G c.(5659-5661)tcA>tcG p.S1887S READ 16 3779578 3779578 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3779578C>T c.5470G>A c.(5470-5472)Gcc>Acc p.A1824T READ 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AH-6549-01A-11D-1826-10 TCGA-AH-6549-10A-01D-1826-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G READ 16 3786078 3786078 + Missense_Mutation SNP T T C TCGA-AH-6643-01A-11D-1826-10 TCGA-AH-6643-11A-01D-1826-10 g.chr16:3786078T>C c.4687A>G c.(4687-4689)Agg>Ggg p.R1563G READ 16 3786763 3786763 + Missense_Mutation SNP A A G TCGA-F5-6812-01A-11D-1826-10 TCGA-F5-6812-10A-01D-1826-10 g.chr16:3786763A>G c.4448T>C c.(4447-4449)aTc>aCc p.I1483T READ 16 3786783 3786783 + Silent SNP T T A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:3786783T>A c.4428A>T c.(4426-4428)ccA>ccT p.P1476P READ 16 3788618 3788618 + Missense_Mutation SNP G G T TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr16:3788618G>T c.4336C>A c.(4336-4338)Cgc>Agc p.R1446S READ 16 3789726 3789726 + Splice_Site SNP C C T TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr16:3789726C>T c.e25-1 READ 16 3790511 3790511 + Missense_Mutation SNP C C A TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr16:3790511C>A c.4022G>T c.(4021-4023)cGa>cTa p.R1341L READ 16 3801731 3801731 + Nonsense_Mutation SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr16:3801731G>A c.3775C>T c.(3775-3777)Cag>Tag p.Q1259* READ 16 3817735 3817735 + Missense_Mutation SNP T T C TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:3817735T>C c.3236A>G c.(3235-3237)cAg>cGg p.Q1079R READ 16 3817735 3817735 + Missense_Mutation SNP T T C TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr16:3817735T>C c.3236A>G c.(3235-3237)cAg>cGg p.Q1079R READ 16 3820703 3820703 + Silent SNP A A G TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3820703A>G c.2748T>C c.(2746-2748)ccT>ccC p.P916P READ 16 3828111 3828111 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr16:3828111G>A c.2014C>T c.(2014-2016)Cgt>Tgt p.R672C READ 16 3900775 3900775 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3900775C>T c.321G>A c.(319-321)ccG>ccA p.P107P READ 16 3900860 3900860 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3900860C>A c.236G>T c.(235-237)gGc>gTc p.G79V SARC 16 3779184 3779184 + Missense_Mutation SNP G G A TCGA-3B-A9HL-01A-11D-A387-09 TCGA-3B-A9HL-10A-01D-A38A-09 g.chr16:3779184G>A c.5864C>T c.(5863-5865)gCg>gTg p.A1955V SARC 16 3819196 3819196 + Frame_Shift_Del DEL G G - TCGA-QC-A6FX-01A-11D-A32I-09 TCGA-QC-A6FX-10B-01D-A32I-09 g.chr16:3819196delG c.3039delC c.(3037-3039)tccfs p.S1013fs SARC 16 3832702 3832702 + Missense_Mutation SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr16:3832702C>T c.1556G>A c.(1555-1557)aGg>aAg p.R519K SARC 16 3900553 3900553 + Frame_Shift_Del DEL A A - TCGA-DX-AB2J-01A-11D-A387-09 TCGA-DX-AB2J-10A-01D-A38A-09 g.chr16:3900553delA c.543delT c.(541-543)tttfs p.F181fs SKCM 16 3777725 3777725 + Silent SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr16:3777725G>A c.7323C>T c.(7321-7323)ggC>ggT p.G2441G SKCM 16 3777767 3777767 + Silent SNP G G A TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr16:3777767G>A c.7281C>T c.(7279-7281)gtC>gtT p.V2427V SKCM 16 3777936 3777936 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3777936G>A c.7112C>T c.(7111-7113)cCt>cTt p.P2371L SKCM 16 3777962 3777962 + Silent SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr16:3777962G>A c.7086C>T c.(7084-7086)agC>agT p.S2362S SKCM 16 3778043 3778043 + Silent SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr16:3778043G>A c.7005C>T c.(7003-7005)atC>atT p.I2335I SKCM 16 3778737 3778737 + Missense_Mutation SNP C C G TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr16:3778737C>G c.6311G>C c.(6310-6312)cGc>cCc p.R2104P SKCM 16 3778993 3778993 + Missense_Mutation SNP C C A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr16:3778993C>A c.6055G>T c.(6055-6057)Ggg>Tgg p.G2019W SKCM 16 3779649 3779649 + Missense_Mutation SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr16:3779649C>T c.5399G>A c.(5398-5400)cGg>cAg p.R1800Q SKCM 16 3779715 3779715 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:3779715G>A c.5333C>T c.(5332-5334)tCg>tTg p.S1778L SKCM 16 3786113 3786113 + Missense_Mutation SNP T T C TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr16:3786113T>C c.4652A>G c.(4651-4653)gAg>gGg p.E1551G SKCM 16 3786779 3786779 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr16:3786779C>T c.4432G>A c.(4432-4434)Gaa>Aaa p.E1478K SKCM 16 3788618 3788618 + Missense_Mutation SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr16:3788618G>A c.4336C>T c.(4336-4338)Cgc>Tgc p.R1446C SKCM 16 3790455 3790455 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3790455G>A c.4078C>T c.(4078-4080)Cga>Tga p.R1360* SKCM 16 3794898 3794898 + Nonsense_Mutation SNP T T A TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr16:3794898T>A c.3979A>T c.(3979-3981)Aag>Tag p.K1327* SKCM 16 3795308 3795308 + Missense_Mutation SNP A A G TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr16:3795308A>G c.3884T>C c.(3883-3885)gTt>gCt p.V1295A SKCM 16 3795352 3795352 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3795352G>A c.3840C>T c.(3838-3840)ttC>ttT p.F1280F SKCM 16 3808895 3808895 + Missense_Mutation SNP G G C TCGA-D3-A2J7-06A-11D-A196-08 TCGA-D3-A2J7-10A-01D-A198-08 g.chr16:3808895G>C c.3329C>G c.(3328-3330)cCt>cGt p.P1110R SKCM 16 3817765 3817765 + Missense_Mutation SNP C C T TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr16:3817765C>T c.3206G>A c.(3205-3207)gGc>gAc p.G1069D SKCM 16 3819272 3819272 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr16:3819272G>A c.2963C>T c.(2962-2964)cCa>cTa p.P988L SKCM 16 3820669 3820669 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr16:3820669G>A c.2782C>T c.(2782-2784)Ccg>Tcg p.P928S SKCM 16 3824617 3824617 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr16:3824617G>A c.2236C>T c.(2236-2238)Cca>Tca p.P746S SKCM 16 3827650 3827650 + Silent SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr16:3827650G>A c.2122C>T c.(2122-2124)Ctg>Ttg p.L708L SKCM 16 3828033 3828033 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr16:3828033C>T c.2092G>A c.(2092-2094)Gca>Aca p.A698T SKCM 16 3828034 3828034 + Silent SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr16:3828034C>T c.2091G>A c.(2089-2091)caG>caA p.Q697Q SKCM 16 3828061 3828061 + Silent SNP C C T TCGA-D3-A1Q8-06A-11D-A19A-08 TCGA-D3-A1Q8-10A-01D-A19A-08 g.chr16:3828061C>T c.2064G>A c.(2062-2064)ccG>ccA p.P688P SKCM 16 3828796 3828796 + Missense_Mutation SNP G G A TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr16:3828796G>A c.1846C>T c.(1846-1848)Cct>Tct p.P616S SKCM 16 3832835 3832835 + Missense_Mutation SNP G G A TCGA-D9-A3Z3-06A-11D-A23B-08 TCGA-D9-A3Z3-10A-01D-A23B-08 g.chr16:3832835G>A c.1423C>T c.(1423-1425)Ccc>Tcc p.P475S SKCM 16 3842066 3842066 + Missense_Mutation SNP T T C TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr16:3842066T>C c.1246A>G c.(1246-1248)Atc>Gtc p.I416V SKCM 16 3843402 3843402 + Missense_Mutation SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr16:3843402C>A c.1201G>T c.(1201-1203)Ggg>Tgg p.G401W SKCM 16 3860727 3860727 + Silent SNP T T A TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr16:3860727T>A c.852A>T c.(850-852)ggA>ggT p.G284G SKCM 16 3900298 3900298 + Splice_Site SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:3900298C>T c.798G>A c.(796-798)aaG>aaA p.K266K SKCM 16 3900527 3900527 + Missense_Mutation SNP T T A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr16:3900527T>A c.569A>T c.(568-570)aAt>aTt p.N190I SKCM 16 3900705 3900705 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:3900705G>A c.391C>T c.(391-393)Ccc>Tcc p.P131S SKCM 16 3900838 3900838 + Silent SNP T T A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr16:3900838T>A c.258A>T c.(256-258)atA>atT p.I86I

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 16 3788617 3788617 single base substitution C T downstream_gene_variant ALL-US 16 3788617 3788617 single base substitution C T intron_variant ALL-US 16 3788617 3788617 single base substitution C T missense_variant R1408H 4223G>A ALL-US 16 3788617 3788617 single base substitution C T missense_variant R1446H 4337G>A ALL-US 16 3788617 3788617 single base substitution C T upstream_gene_variant ALL-US 16 3788632 3788632 single base substitution C G downstream_gene_variant ALL-US 16 3788632 3788632 single base substitution C G intron_variant ALL-US 16 3788632 3788632 single base substitution C G missense_variant R1403P 4208G>C ALL-US 16 3788632 3788632 single base substitution C G missense_variant R1441P 4322G>C ALL-US 16 3788632 3788632 single base substitution C G upstream_gene_variant ALL-US 16 3801783 3801783 single base substitution G A intron_variant ALL-US 16 3801783 3801783 single base substitution G A synonymous_variant F1203F 3609C>T ALL-US 16 3801783 3801783 single base substitution G A synonymous_variant F1241F 3723C>T ALL-US 16 3801783 3801783 single base substitution G A synonymous_variant F9F 27C>T AML-US 16 3779612 3779612 single base substitution G A downstream_gene_variant AML-US 16 3779612 3779612 single base substitution G A synonymous_variant T1774T 5322C>T AML-US 16 3779612 3779612 single base substitution G A synonymous_variant T1812T 5436C>T AML-US 16 3830795 3830795 insertion of <=200bp - C frameshift_variant G24G? AML-US 16 3830795 3830795 insertion of <=200bp - C frameshift_variant G549G? AML-US 16 3830795 3830795 insertion of <=200bp - C frameshift_variant G587G? AML-US 16 3830795 3830795 insertion of <=200bp - C upstream_gene_variant BLCA-CN 16 3778065 3778065 single base substitution G A downstream_gene_variant BLCA-CN 16 3778065 3778065 single base substitution G A missense_variant S2290L 6869C>T BLCA-CN 16 3778065 3778065 single base substitution G A missense_variant S2328L 6983C>T BLCA-CN 16 3778535 3778535 single base substitution C T downstream_gene_variant BLCA-CN 16 3778535 3778535 single base substitution C T synonymous_variant L2133L 6399G>A BLCA-CN 16 3778535 3778535 single base substitution C T synonymous_variant L2171L 6513G>A BLCA-CN 16 3786705 3786705 single base substitution C A downstream_gene_variant BLCA-CN 16 3786705 3786705 single base substitution C A exon_variant BLCA-CN 16 3786705 3786705 single base substitution C A missense_variant W1464C 4392G>T BLCA-CN 16 3786705 3786705 single base substitution C A missense_variant W1502C 4506G>T BLCA-CN 16 3788618 3788618 single base substitution G C downstream_gene_variant BLCA-CN 16 3788618 3788618 single base substitution G C intron_variant BLCA-CN 16 3788618 3788618 single base substitution G C missense_variant R1408G 4222C>G BLCA-CN 16 3788618 3788618 single base substitution G C missense_variant R1446G 4336C>G BLCA-CN 16 3788618 3788618 single base substitution G C upstream_gene_variant BLCA-CN 16 3795318 3795318 single base substitution G A exon_variant BLCA-CN 16 3795318 3795318 single base substitution G A stop_gained Q1254* 3760C>T BLCA-CN 16 3795318 3795318 single base substitution G A stop_gained Q1292* 3874C>T BLCA-CN 16 3795318 3795318 single base substitution G A stop_gained Q165* 493C>T BLCA-CN 16 3795318 3795318 single base substitution G A stop_gained Q60* 178C>T BLCA-CN 16 3795318 3795318 single base substitution G A upstream_gene_variant BLCA-CN 16 3801726 3801726 single base substitution C A intron_variant BLCA-CN 16 3801726 3801726 single base substitution C A splice_donor_variant BLCA-CN 16 3807298 3807298 single base substitution T C intron_variant BLCA-CN 16 3807298 3807298 single base substitution T C missense_variant Y1192C 3575A>G BLCA-CN 16 3807298 3807298 single base substitution T C missense_variant Y1230C 3689A>G BLCA-CN 16 3807902 3807902 single base substitution G A stop_gained R1135* 3403C>T BLCA-CN 16 3807902 3807902 single base substitution G A stop_gained R1173* 3517C>T BLCA-CN 16 3807902 3807902 single base substitution G A stop_gained R127* 379C>T BLCA-CN 16 3808901 3808901 single base substitution G T stop_gained S1070* 3209C>A BLCA-CN 16 3808901 3808901 single base substitution G T stop_gained S1108* 3323C>A BLCA-CN 16 3808901 3808901 single base substitution G T stop_gained S62* 185C>A BLCA-CN 16 3817754 3817754 single base substitution G A exon_variant BLCA-CN 16 3817754 3817754 single base substitution G A stop_gained Q1035* 3103C>T BLCA-CN 16 3817754 3817754 single base substitution G A stop_gained Q1073* 3217C>T BLCA-CN 16 3817754 3817754 single base substitution G A stop_gained Q27* 79C>T BLCA-CN 16 3820936 3820936 single base substitution G A downstream_gene_variant BLCA-CN 16 3820936 3820936 single base substitution G A stop_gained Q801* 2401C>T BLCA-CN 16 3820936 3820936 single base substitution G A stop_gained Q839* 2515C>T BLCA-CN 16 3820936 3820936 single base substitution G A upstream_gene_variant BLCA-CN 16 3842054 3842054 single base substitution T A intron_variant BLCA-CN 16 3842054 3842054 single base substitution T A stop_gained K420* 1258A>T BLCA-CN 16 3843540 3843540 single base substitution G A stop_gained Q355* 1063C>T BLCA-CN 16 3900786 3900786 single base substitution G A stop_gained Q104* 310C>T BLCA-CN 16 3900810 3900810 single base substitution G A stop_gained Q96* 286C>T BLCA-US 16 3777746 3777746 single base substitution C T downstream_gene_variant BLCA-US 16 3777746 3777746 single base substitution C T synonymous_variant T2396T 7188G>A BLCA-US 16 3777746 3777746 single base substitution C T synonymous_variant T2434T 7302G>A BLCA-US 16 3779153 3779153 single base substitution C T downstream_gene_variant BLCA-US 16 3779153 3779153 single base substitution C T synonymous_variant E1927E 5781G>A BLCA-US 16 3779153 3779153 single base substitution C T synonymous_variant E1965E 5895G>A BLCA-US 16 3820952 3820952 single base substitution G C downstream_gene_variant BLCA-US 16 3820952 3820952 single base substitution G C synonymous_variant L795L 2385C>G BLCA-US 16 3820952 3820952 single base substitution G C synonymous_variant L833L 2499C>G BLCA-US 16 3820952 3820952 single base substitution G C upstream_gene_variant BLCA-US 16 3828084 3828084 insertion of <=200bp - C frameshift_variant N118R? BLCA-US 16 3828084 3828084 insertion of <=200bp - C frameshift_variant N30R? BLCA-US 16 3828084 3828084 insertion of <=200bp - C frameshift_variant N643R? BLCA-US 16 3828084 3828084 insertion of <=200bp - C frameshift_variant N681R? BLCA-US 16 3828084 3828084 insertion of <=200bp - C upstream_gene_variant BRCA-EU 16 3770294 3770294 single base substitution G C downstream_gene_variant BRCA-EU 16 3770711 3770711 single base substitution G A downstream_gene_variant BRCA-EU 16 3770821 3770821 single base substitution C A downstream_gene_variant BRCA-EU 16 3771918 3771918 single base substitution C G downstream_gene_variant BRCA-EU 16 3772038 3772038 single base substitution C A downstream_gene_variant BRCA-EU 16 3773021 3773021 single base substitution C G downstream_gene_variant BRCA-EU 16 3774163 3774163 single base substitution C A downstream_gene_variant BRCA-EU 16 3776284 3776284 deletion of <=200bp G - 3_prime_UTR_variant BRCA-EU 16 3776284 3776284 deletion of <=200bp G - downstream_gene_variant BRCA-EU 16 3779137 3779137 single base substitution G A downstream_gene_variant BRCA-EU 16 3779137 3779137 single base substitution G A missense_variant H1933Y 5797C>T BRCA-EU 16 3779137 3779137 single base substitution G A missense_variant H1971Y 5911C>T BRCA-EU 16 3780492 3780492 single base substitution C A downstream_gene_variant BRCA-EU 16 3780492 3780492 single base substitution C A intron_variant BRCA-EU 16 3781995 3781995 single base substitution G T downstream_gene_variant BRCA-EU 16 3781995 3781995 single base substitution G T intron_variant BRCA-EU 16 3783149 3783149 single base substitution G T downstream_gene_variant BRCA-EU 16 3783149 3783149 single base substitution G T intron_variant BRCA-EU 16 3783231 3783231 single base substitution C T downstream_gene_variant BRCA-EU 16 3783231 3783231 single base substitution C T intron_variant BRCA-EU 16 3785174 3785174 single base substitution C T downstream_gene_variant BRCA-EU 16 3785174 3785174 single base substitution C T intron_variant BRCA-EU 16 3785988 3785988 single base substitution C G downstream_gene_variant BRCA-EU 16 3785988 3785988 single base substitution C G intron_variant BRCA-EU 16 3789582 3789582 single base substitution G A downstream_gene_variant BRCA-EU 16 3789582 3789582 single base substitution G A exon_variant BRCA-EU 16 3789582 3789582 single base substitution G A intron_variant BRCA-EU 16 3789582 3789582 single base substitution G A missense_variant T1388M 4163C>T BRCA-EU 16 3789582 3789582 single base substitution G A missense_variant T1426M 4277C>T BRCA-EU 16 3789582 3789582 single base substitution G A missense_variant T194M 581C>T BRCA-EU 16 3789582 3789582 single base substitution G A upstream_gene_variant BRCA-EU 16 3791711 3791711 single base substitution C T exon_variant BRCA-EU 16 3791711 3791711 single base substitution C T intron_variant BRCA-EU 16 3791711 3791711 single base substitution C T upstream_gene_variant BRCA-EU 16 3792145 3792145 single base substitution C T exon_variant BRCA-EU 16 3792145 3792145 single base substitution C T intron_variant BRCA-EU 16 3792226 3792226 single base substitution G A exon_variant BRCA-EU 16 3792226 3792226 single base substitution G A intron_variant BRCA-EU 16 3796323 3796323 single base substitution G A intron_variant BRCA-EU 16 3796323 3796323 single base substitution G A upstream_gene_variant BRCA-EU 16 3796439 3796440 deletion of <=200bp CC - intron_variant BRCA-EU 16 3796439 3796440 deletion of <=200bp CC - upstream_gene_variant BRCA-EU 16 3796512 3796512 single base substitution G C intron_variant BRCA-EU 16 3796512 3796512 single base substitution G C upstream_gene_variant BRCA-EU 16 3796813 3796813 single base substitution G A intron_variant BRCA-EU 16 3796813 3796813 single base substitution G A upstream_gene_variant BRCA-EU 16 3797906 3797906 single base substitution T C intron_variant BRCA-EU 16 3797906 3797906 single base substitution T C upstream_gene_variant BRCA-EU 16 3798775 3798775 single base substitution A C intron_variant BRCA-EU 16 3798775 3798775 single base substitution A C upstream_gene_variant BRCA-EU 16 3799734 3799734 single base substitution G C intron_variant BRCA-EU 16 3799734 3799734 single base substitution G C upstream_gene_variant BRCA-EU 16 3799895 3799895 single base substitution C G intron_variant BRCA-EU 16 3799895 3799895 single base substitution C G upstream_gene_variant BRCA-EU 16 3801151 3801151 single base substitution C T intron_variant BRCA-EU 16 3802349 3802349 single base substitution G A intron_variant BRCA-EU 16 3802349 3802349 single base substitution G A upstream_gene_variant BRCA-EU 16 3804480 3804480 single base substitution T G intron_variant BRCA-EU 16 3804480 3804480 single base substitution T G upstream_gene_variant BRCA-EU 16 3804519 3804519 single base substitution T C intron_variant BRCA-EU 16 3804519 3804519 single base substitution T C upstream_gene_variant BRCA-EU 16 3805981 3805981 insertion of <=200bp - A intron_variant BRCA-EU 16 3805981 3805981 insertion of <=200bp - A upstream_gene_variant BRCA-EU 16 3806607 3806607 single base substitution C T intron_variant BRCA-EU 16 3806607 3806607 single base substitution C T upstream_gene_variant BRCA-EU 16 3806830 3806830 single base substitution G C intron_variant BRCA-EU 16 3807078 3807078 single base substitution C T intron_variant BRCA-EU 16 3807189 3807189 deletion of <=200bp T - intron_variant BRCA-EU 16 3807364 3807364 insertion of <=200bp - G frameshift_variant P1170P? BRCA-EU 16 3807364 3807364 insertion of <=200bp - G frameshift_variant P1208P? BRCA-EU 16 3807364 3807364 insertion of <=200bp - G intron_variant BRCA-EU 16 3811661 3811661 single base substitution G A intron_variant BRCA-EU 16 3812129 3812129 insertion of <=200bp - GCT intron_variant BRCA-EU 16 3813169 3813169 single base substitution A T downstream_gene_variant BRCA-EU 16 3813169 3813169 single base substitution A T intron_variant BRCA-EU 16 3813449 3813449 single base substitution C G downstream_gene_variant BRCA-EU 16 3813449 3813449 single base substitution C G intron_variant BRCA-EU 16 3814033 3814033 single base substitution G C downstream_gene_variant BRCA-EU 16 3814033 3814033 single base substitution G C intron_variant BRCA-EU 16 3814080 3814080 single base substitution G A downstream_gene_variant BRCA-EU 16 3814080 3814080 single base substitution G A intron_variant BRCA-EU 16 3814641 3814641 single base substitution A G downstream_gene_variant BRCA-EU 16 3814641 3814641 single base substitution A G intron_variant BRCA-EU 16 3815015 3815015 single base substitution C G downstream_gene_variant BRCA-EU 16 3815015 3815015 single base substitution C G intron_variant BRCA-EU 16 3815035 3815035 single base substitution C T downstream_gene_variant BRCA-EU 16 3815035 3815035 single base substitution C T intron_variant BRCA-EU 16 3816054 3816054 deletion of <=200bp T - downstream_gene_variant BRCA-EU 16 3816054 3816054 deletion of <=200bp T - intron_variant BRCA-EU 16 3816123 3816123 deletion of <=200bp A - downstream_gene_variant BRCA-EU 16 3816123 3816123 deletion of <=200bp A - intron_variant BRCA-EU 16 3817354 3817354 single base substitution T G exon_variant BRCA-EU 16 3817354 3817354 single base substitution T G intron_variant BRCA-EU 16 3817476 3817476 single base substitution C G exon_variant BRCA-EU 16 3817476 3817476 single base substitution C G intron_variant BRCA-EU 16 3817655 3817655 single base substitution C A exon_variant BRCA-EU 16 3817655 3817655 single base substitution C A intron_variant BRCA-EU 16 3817721 3817721 deletion of <=200bp T - exon_variant BRCA-EU 16 3817721 3817721 deletion of <=200bp T - frameshift_variant I1046 BRCA-EU 16 3817721 3817721 deletion of <=200bp T - frameshift_variant I1084 BRCA-EU 16 3817721 3817721 deletion of <=200bp T - frameshift_variant I38 BRCA-EU 16 3818046 3818046 single base substitution C G intron_variant BRCA-EU 16 3818046 3818046 single base substitution C G upstream_gene_variant BRCA-EU 16 3820417 3820417 single base substitution G C downstream_gene_variant BRCA-EU 16 3820417 3820417 single base substitution G C intron_variant BRCA-EU 16 3820417 3820417 single base substitution G C upstream_gene_variant BRCA-EU 16 3820624 3820624 single base substitution G A downstream_gene_variant BRCA-EU 16 3820624 3820624 single base substitution G A exon_variant BRCA-EU 16 3820624 3820624 single base substitution G A stop_gained Q905* 2713C>T BRCA-EU 16 3820624 3820624 single base substitution G A stop_gained Q943* 2827C>T BRCA-EU 16 3820624 3820624 single base substitution G A upstream_gene_variant BRCA-EU 16 3821028 3821028 single base substitution G A downstream_gene_variant BRCA-EU 16 3821028 3821028 single base substitution G A intron_variant BRCA-EU 16 3821028 3821028 single base substitution G A upstream_gene_variant BRCA-EU 16 3821078 3821078 single base substitution T A downstream_gene_variant BRCA-EU 16 3821078 3821078 single base substitution T A intron_variant BRCA-EU 16 3821078 3821078 single base substitution T A upstream_gene_variant BRCA-EU 16 3821402 3821402 single base substitution G C downstream_gene_variant BRCA-EU 16 3821402 3821402 single base substitution G C intron_variant BRCA-EU 16 3821402 3821402 single base substitution G C upstream_gene_variant BRCA-EU 16 3823754 3823754 single base substitution G A exon_variant BRCA-EU 16 3823754 3823754 single base substitution G A stop_gained Q170* 508C>T BRCA-EU 16 3823754 3823754 single base substitution G A stop_gained Q243* 727C>T BRCA-EU 16 3823754 3823754 single base substitution G A stop_gained Q783* 2347C>T BRCA-EU 16 3823754 3823754 single base substitution G A stop_gained Q821* 2461C>T BRCA-EU 16 3823754 3823754 single base substitution G A upstream_gene_variant BRCA-EU 16 3824314 3824314 single base substitution C T intron_variant BRCA-EU 16 3824314 3824314 single base substitution C T upstream_gene_variant BRCA-EU 16 3824754 3824754 single base substitution A T intron_variant BRCA-EU 16 3824754 3824754 single base substitution A T upstream_gene_variant BRCA-EU 16 3824843 3824843 single base substitution G A intron_variant BRCA-EU 16 3824843 3824843 single base substitution G A upstream_gene_variant BRCA-EU 16 3825854 3825854 single base substitution G T intron_variant BRCA-EU 16 3825854 3825854 single base substitution G T upstream_gene_variant BRCA-EU 16 3827394 3827394 single base substitution T A intron_variant BRCA-EU 16 3827394 3827394 single base substitution T A upstream_gene_variant BRCA-EU 16 3828367 3828367 single base substitution C A intron_variant BRCA-EU 16 3828367 3828367 single base substitution C A upstream_gene_variant BRCA-EU 16 3829740 3829740 deletion of <=200bp A - intron_variant BRCA-EU 16 3829740 3829740 deletion of <=200bp A - upstream_gene_variant BRCA-EU 16 3831215 3831215 single base substitution C T missense_variant G518R 1552G>A BRCA-EU 16 3831215 3831215 single base substitution C T missense_variant G556R 1666G>A BRCA-EU 16 3831215 3831215 single base substitution C T upstream_gene_variant BRCA-EU 16 3832419 3832419 single base substitution A G intron_variant BRCA-EU 16 3832419 3832419 single base substitution A G upstream_gene_variant BRCA-EU 16 3832943 3832943 single base substitution G A intron_variant BRCA-EU 16 3832943 3832943 single base substitution G A upstream_gene_variant BRCA-EU 16 3833009 3833009 single base substitution G C intron_variant BRCA-EU 16 3833009 3833009 single base substitution G C upstream_gene_variant BRCA-EU 16 3833105 3833105 single base substitution C T intron_variant BRCA-EU 16 3833105 3833105 single base substitution C T upstream_gene_variant BRCA-EU 16 3835685 3835685 single base substitution C A intron_variant BRCA-EU 16 3835685 3835685 single base substitution C A upstream_gene_variant BRCA-EU 16 3835919 3835919 single base substitution C T intron_variant BRCA-EU 16 3837581 3837581 single base substitution G C intron_variant BRCA-EU 16 3838511 3838511 single base substitution C A intron_variant BRCA-EU 16 3838787 3838787 single base substitution T C intron_variant BRCA-EU 16 3839886 3839886 single base substitution A T intron_variant BRCA-EU 16 3839916 3839916 single base substitution C G intron_variant BRCA-EU 16 3840352 3840352 single base substitution C G intron_variant BRCA-EU 16 3841156 3841156 single base substitution C G intron_variant BRCA-EU 16 3843102 3843102 single base substitution C T intron_variant BRCA-EU 16 3843961 3843961 single base substitution T A intron_variant BRCA-EU 16 3844482 3844482 single base substitution T A intron_variant BRCA-EU 16 3845290 3845290 single base substitution T C intron_variant BRCA-EU 16 3846617 3846617 single base substitution A T intron_variant BRCA-EU 16 3846651 3846651 single base substitution G A intron_variant BRCA-EU 16 3847243 3847243 single base substitution T C intron_variant BRCA-EU 16 3847488 3847488 single base substitution C T intron_variant BRCA-EU 16 3847775 3847775 single base substitution T G intron_variant BRCA-EU 16 3849050 3849050 single base substitution C A intron_variant BRCA-EU 16 3849483 3849483 single base substitution C T intron_variant BRCA-EU 16 3851468 3851468 single base substitution G C intron_variant BRCA-EU 16 3853903 3853903 single base substitution G A intron_variant BRCA-EU 16 3853919 3853919 deletion of <=200bp A - intron_variant BRCA-EU 16 3854347 3854347 insertion of <=200bp - A intron_variant BRCA-EU 16 3854882 3854882 single base substitution A T intron_variant BRCA-EU 16 3854990 3854990 single base substitution G C intron_variant BRCA-EU 16 3858374 3858374 single base substitution G C intron_variant BRCA-EU 16 3858453 3858453 single base substitution A G intron_variant BRCA-EU 16 3859062 3859062 single base substitution G C intron_variant BRCA-EU 16 3860247 3860247 single base substitution G A intron_variant BRCA-EU 16 3861410 3861410 single base substitution G C intron_variant BRCA-EU 16 3861730 3861730 single base substitution G C intron_variant BRCA-EU 16 3861733 3861733 single base substitution G A intron_variant BRCA-EU 16 3861735 3861735 single base substitution T A intron_variant BRCA-EU 16 3863289 3863289 single base substitution G A intron_variant BRCA-EU 16 3863604 3863604 deletion of <=200bp T - intron_variant BRCA-EU 16 3864362 3864362 single base substitution T G intron_variant BRCA-EU 16 3864804 3864804 single base substitution G A intron_variant BRCA-EU 16 3869329 3869329 single base substitution C T intron_variant BRCA-EU 16 3870199 3870199 single base substitution T G intron_variant BRCA-EU 16 3870569 3870569 single base substitution G A intron_variant BRCA-EU 16 3870623 3870623 single base substitution G C intron_variant BRCA-EU 16 3871756 3871756 single base substitution C T intron_variant BRCA-EU 16 3872088 3872088 single base substitution A G intron_variant BRCA-EU 16 3872393 3872393 single base substitution G A intron_variant BRCA-EU 16 3872616 3872616 single base substitution C T intron_variant BRCA-EU 16 3872875 3872875 single base substitution G C intron_variant BRCA-EU 16 3873181 3873181 single base substitution A T intron_variant BRCA-EU 16 3875239 3875239 single base substitution C A intron_variant BRCA-EU 16 3875822 3875822 single base substitution G A intron_variant BRCA-EU 16 3876949 3876949 single base substitution G A intron_variant BRCA-EU 16 3877849 3877849 single base substitution A G intron_variant BRCA-EU 16 3879474 3879474 single base substitution G A intron_variant BRCA-EU 16 3880921 3880921 single base substitution C G intron_variant BRCA-EU 16 3881138 3881138 single base substitution G C intron_variant BRCA-EU 16 3882372 3882372 insertion of <=200bp - A intron_variant BRCA-EU 16 3882435 3882435 single base substitution A G intron_variant BRCA-EU 16 3883050 3883050 single base substitution G A intron_variant BRCA-EU 16 3883902 3883902 single base substitution A G intron_variant BRCA-EU 16 3884227 3884227 single base substitution G C intron_variant BRCA-EU 16 3887788 3887788 single base substitution G A intron_variant BRCA-EU 16 3888331 3888331 single base substitution T C intron_variant BRCA-EU 16 3890195 3890195 single base substitution G A intron_variant BRCA-EU 16 3891006 3891006 single base substitution C T intron_variant BRCA-EU 16 3891029 3891029 single base substitution C T intron_variant BRCA-EU 16 3891542 3891542 single base substitution T A intron_variant BRCA-EU 16 3892913 3892913 single base substitution G C intron_variant BRCA-EU 16 3894271 3894271 single base substitution G C intron_variant BRCA-EU 16 3894492 3894492 single base substitution C T intron_variant BRCA-EU 16 3894635 3894635 deletion of <=200bp A - intron_variant BRCA-EU 16 3894659 3894659 single base substitution A G intron_variant BRCA-EU 16 3896673 3896673 single base substitution G C intron_variant BRCA-EU 16 3896689 3896689 single base substitution G A intron_variant BRCA-EU 16 3896985 3896985 single base substitution G A intron_variant BRCA-EU 16 3897448 3897448 single base substitution T C intron_variant BRCA-EU 16 3898441 3898441 single base substitution A T intron_variant BRCA-EU 16 3898807 3898807 single base substitution T C intron_variant BRCA-EU 16 3898893 3898893 single base substitution G C intron_variant BRCA-EU 16 3899613 3899613 single base substitution C G intron_variant BRCA-EU 16 3902319 3902319 single base substitution A G intron_variant BRCA-EU 16 3903669 3903669 single base substitution A G intron_variant BRCA-EU 16 3903675 3903675 single base substitution T C intron_variant BRCA-EU 16 3903676 3903676 single base substitution G A intron_variant BRCA-EU 16 3904274 3904274 single base substitution G C intron_variant BRCA-EU 16 3904424 3904424 single base substitution C G intron_variant BRCA-EU 16 3906331 3906331 single base substitution T C intron_variant BRCA-EU 16 3906425 3906425 single base substitution G C intron_variant BRCA-EU 16 3907611 3907611 single base substitution G C intron_variant BRCA-EU 16 3907915 3907915 single base substitution A C intron_variant BRCA-EU 16 3908401 3908401 single base substitution G A intron_variant BRCA-EU 16 3908733 3908733 single base substitution G C intron_variant BRCA-EU 16 3909441 3909441 single base substitution C T intron_variant BRCA-EU 16 3909546 3909546 single base substitution G C intron_variant BRCA-EU 16 3910328 3910328 single base substitution G A intron_variant BRCA-EU 16 3910653 3910653 single base substitution A C intron_variant BRCA-EU 16 3911271 3911271 single base substitution A C intron_variant BRCA-EU 16 3915237 3915237 single base substitution C T intron_variant BRCA-EU 16 3915599 3915599 single base substitution G A intron_variant BRCA-EU 16 3915695 3915695 single base substitution A C intron_variant BRCA-EU 16 3915927 3915927 single base substitution G A intron_variant BRCA-EU 16 3917206 3917206 single base substitution G C intron_variant BRCA-EU 16 3918031 3918031 single base substitution G C intron_variant BRCA-EU 16 3920562 3920562 single base substitution G A intron_variant BRCA-EU 16 3921491 3921491 single base substitution A T intron_variant BRCA-EU 16 3924325 3924325 single base substitution G A intron_variant BRCA-EU 16 3924422 3924422 single base substitution A G intron_variant BRCA-EU 16 3925552 3925552 single base substitution T G intron_variant BRCA-EU 16 3926507 3926507 single base substitution T C intron_variant BRCA-EU 16 3926626 3926626 single base substitution A C intron_variant BRCA-EU 16 3926850 3926850 single base substitution G A intron_variant BRCA-EU 16 3927008 3927008 single base substitution G A intron_variant BRCA-EU 16 3928594 3928594 deletion of <=200bp T - intron_variant BRCA-EU 16 3928919 3928919 single base substitution G T intron_variant BRCA-EU 16 3929000 3929000 insertion of <=200bp - T intron_variant BRCA-EU 16 3929330 3929330 single base substitution C A intron_variant BRCA-EU 16 3929703 3929703 single base substitution G A intron_variant BRCA-EU 16 3930777 3930777 insertion of <=200bp - G upstream_gene_variant BRCA-EU 16 3930927 3930927 single base substitution C T upstream_gene_variant BRCA-EU 16 3931881 3931881 single base substitution T A upstream_gene_variant BRCA-EU 16 3932020 3932020 single base substitution G A upstream_gene_variant BRCA-EU 16 3933818 3933818 single base substitution C T upstream_gene_variant BRCA-EU 16 3934406 3934406 single base substitution G T upstream_gene_variant BRCA-EU 16 3935425 3935425 single base substitution G T upstream_gene_variant BRCA-FR 16 3770294 3770294 single base substitution G C downstream_gene_variant BRCA-FR 16 3772038 3772038 single base substitution C A downstream_gene_variant BRCA-FR 16 3774395 3774395 single base substitution G T downstream_gene_variant BRCA-FR 16 3789582 3789582 single base substitution G A downstream_gene_variant BRCA-FR 16 3789582 3789582 single base substitution G A exon_variant BRCA-FR 16 3789582 3789582 single base substitution G A intron_variant BRCA-FR 16 3789582 3789582 single base substitution G A missense_variant T1388M 4163C>T BRCA-FR 16 3789582 3789582 single base substitution G A missense_variant T1426M 4277C>T BRCA-FR 16 3789582 3789582 single base substitution G A missense_variant T194M 581C>T BRCA-FR 16 3789582 3789582 single base substitution G A upstream_gene_variant BRCA-FR 16 3792145 3792145 single base substitution C T exon_variant BRCA-FR 16 3792145 3792145 single base substitution C T intron_variant BRCA-FR 16 3796512 3796512 single base substitution G C intron_variant BRCA-FR 16 3796512 3796512 single base substitution G C upstream_gene_variant BRCA-FR 16 3799895 3799895 single base substitution C G intron_variant BRCA-FR 16 3799895 3799895 single base substitution C G upstream_gene_variant BRCA-FR 16 3801151 3801151 single base substitution C T intron_variant BRCA-FR 16 3802349 3802349 single base substitution G A intron_variant BRCA-FR 16 3802349 3802349 single base substitution G A upstream_gene_variant BRCA-FR 16 3806830 3806830 single base substitution G C intron_variant BRCA-FR 16 3819586 3819586 single base substitution G C downstream_gene_variant BRCA-FR 16 3819586 3819586 single base substitution G C intron_variant BRCA-FR 16 3819586 3819586 single base substitution G C upstream_gene_variant BRCA-FR 16 3821028 3821028 single base substitution G A downstream_gene_variant BRCA-FR 16 3821028 3821028 single base substitution G A intron_variant BRCA-FR 16 3821028 3821028 single base substitution G A upstream_gene_variant BRCA-FR 16 3825854 3825854 single base substitution G T intron_variant BRCA-FR 16 3825854 3825854 single base substitution G T upstream_gene_variant BRCA-FR 16 3827394 3827394 single base substitution T A intron_variant BRCA-FR 16 3827394 3827394 single base substitution T A upstream_gene_variant BRCA-FR 16 3828367 3828367 single base substitution C A intron_variant BRCA-FR 16 3828367 3828367 single base substitution C A upstream_gene_variant BRCA-FR 16 3831215 3831215 single base substitution C T missense_variant G518R 1552G>A BRCA-FR 16 3831215 3831215 single base substitution C T missense_variant G556R 1666G>A BRCA-FR 16 3831215 3831215 single base substitution C T upstream_gene_variant BRCA-FR 16 3833009 3833009 single base substitution G C intron_variant BRCA-FR 16 3833009 3833009 single base substitution G C upstream_gene_variant BRCA-FR 16 3847020 3847020 single base substitution G T intron_variant BRCA-FR 16 3849050 3849050 single base substitution C A intron_variant BRCA-FR 16 3851468 3851468 single base substitution G C intron_variant BRCA-FR 16 3856918 3856918 single base substitution T A intron_variant BRCA-FR 16 3858188 3858188 single base substitution G C intron_variant BRCA-FR 16 3858374 3858374 single base substitution G C intron_variant BRCA-FR 16 3863632 3863632 single base substitution G A intron_variant BRCA-FR 16 3872875 3872875 single base substitution G C intron_variant BRCA-FR 16 3875751 3875751 single base substitution C A intron_variant BRCA-FR 16 3877496 3877496 single base substitution G C intron_variant BRCA-FR 16 3883902 3883902 single base substitution A G intron_variant BRCA-FR 16 3887788 3887788 single base substitution G A intron_variant BRCA-FR 16 3900075 3900075 single base substitution G A intron_variant BRCA-FR 16 3920562 3920562 single base substitution G A intron_variant BRCA-FR 16 3927287 3927287 single base substitution G C intron_variant BRCA-FR 16 3928919 3928919 single base substitution G T intron_variant BRCA-FR 16 3929330 3929330 single base substitution C A intron_variant BRCA-FR 16 3929703 3929703 single base substitution G A intron_variant BRCA-KR 16 3779843 3779843 single base substitution C T downstream_gene_variant BRCA-KR 16 3779843 3779843 single base substitution C T synonymous_variant T1697T 5091G>A BRCA-KR 16 3779843 3779843 single base substitution C T synonymous_variant T1735T 5205G>A BRCA-UK 16 3772243 3772243 single base substitution C T downstream_gene_variant BRCA-UK 16 3774163 3774163 single base substitution C A downstream_gene_variant BRCA-UK 16 3780406 3780406 single base substitution G A downstream_gene_variant BRCA-UK 16 3780406 3780406 single base substitution G A intron_variant BRCA-UK 16 3786079 3786079 single base substitution C T downstream_gene_variant BRCA-UK 16 3786079 3786079 single base substitution C T exon_variant BRCA-UK 16 3786079 3786079 single base substitution C T synonymous_variant E1524E 4572G>A BRCA-UK 16 3786079 3786079 single base substitution C T synonymous_variant E1562E 4686G>A BRCA-UK 16 3807189 3807189 deletion of <=200bp T - intron_variant BRCA-UK 16 3813449 3813449 single base substitution C G downstream_gene_variant BRCA-UK 16 3813449 3813449 single base substitution C G intron_variant BRCA-UK 16 3814080 3814080 single base substitution G A downstream_gene_variant BRCA-UK 16 3814080 3814080 single base substitution G A intron_variant BRCA-UK 16 3852163 3852163 single base substitution C T intron_variant BRCA-UK 16 3872088 3872088 single base substitution A G intron_variant BRCA-UK 16 3879661 3879661 single base substitution G C intron_variant BRCA-UK 16 3898807 3898807 single base substitution T C intron_variant BRCA-UK 16 3904274 3904274 single base substitution G C intron_variant BRCA-UK 16 3926850 3926850 single base substitution G A intron_variant BRCA-US 16 3777933 3777933 single base substitution G A downstream_gene_variant BRCA-US 16 3777933 3777933 single base substitution G A missense_variant S2334L 7001C>T BRCA-US 16 3777933 3777933 single base substitution G A missense_variant S2372L 7115C>T BRCA-US 16 3778245 3778245 single base substitution A G downstream_gene_variant BRCA-US 16 3778245 3778245 single base substitution A G missense_variant M2230T 6689T>C BRCA-US 16 3778245 3778245 single base substitution A G missense_variant M2268T 6803T>C BRCA-US 16 3778745 3778745 single base substitution G C downstream_gene_variant BRCA-US 16 3778745 3778745 single base substitution G C missense_variant I2063M 6189C>G BRCA-US 16 3778745 3778745 single base substitution G C missense_variant I2101M 6303C>G BRCA-US 16 3778897 3778897 insertion of <=200bp - C downstream_gene_variant BRCA-US 16 3778897 3778897 insertion of <=200bp - C frameshift_variant P2013R? BRCA-US 16 3778897 3778897 insertion of <=200bp - C frameshift_variant P2051R? BRCA-US 16 3779066 3779066 single base substitution C G downstream_gene_variant BRCA-US 16 3779066 3779066 single base substitution C G missense_variant Q1956H 5868G>C BRCA-US 16 3779066 3779066 single base substitution C G missense_variant Q1994H 5982G>C BRCA-US 16 3779642 3779642 single base substitution C G downstream_gene_variant BRCA-US 16 3779642 3779642 single base substitution C G synonymous_variant V1764V 5292G>C BRCA-US 16 3779642 3779642 single base substitution C G synonymous_variant V1802V 5406G>C BRCA-US 16 3781302 3781302 single base substitution G A downstream_gene_variant BRCA-US 16 3781302 3781302 single base substitution G A missense_variant T1650M 4949C>T BRCA-US 16 3781302 3781302 single base substitution G A missense_variant T1688M 5063C>T BRCA-US 16 3781803 3781803 single base substitution A G downstream_gene_variant BRCA-US 16 3781803 3781803 single base substitution A G missense_variant Y1584H 4750T>C BRCA-US 16 3781803 3781803 single base substitution A G missense_variant Y1622H 4864T>C BRCA-US 16 3781889 3781889 single base substitution G T downstream_gene_variant BRCA-US 16 3781889 3781889 single base substitution G T missense_variant T1555N 4664C>A BRCA-US 16 3781889 3781889 single base substitution G T missense_variant T1593N 4778C>A BRCA-US 16 3789684 3789684 single base substitution C T downstream_gene_variant BRCA-US 16 3789684 3789684 single base substitution C T exon_variant BRCA-US 16 3789684 3789684 single base substitution C T intron_variant BRCA-US 16 3789684 3789684 single base substitution C T missense_variant R1354Q 4061G>A BRCA-US 16 3789684 3789684 single base substitution C T missense_variant R1392Q 4175G>A BRCA-US 16 3789684 3789684 single base substitution C T missense_variant R160Q 479G>A BRCA-US 16 3789684 3789684 single base substitution C T missense_variant R265Q 794G>A BRCA-US 16 3789684 3789684 single base substitution C T upstream_gene_variant BRCA-US 16 3795332 3795332 single base substitution C T exon_variant BRCA-US 16 3795332 3795332 single base substitution C T missense_variant G1249D 3746G>A BRCA-US 16 3795332 3795332 single base substitution C T missense_variant G1287D 3860G>A BRCA-US 16 3795332 3795332 single base substitution C T missense_variant G160D 479G>A BRCA-US 16 3795332 3795332 single base substitution C T missense_variant G55D 164G>A BRCA-US 16 3795332 3795332 single base substitution C T upstream_gene_variant BRCA-US 16 3807914 3807914 single base substitution G A missense_variant R1131C 3391C>T BRCA-US 16 3807914 3807914 single base substitution G A missense_variant R1169C 3505C>T BRCA-US 16 3807914 3807914 single base substitution G A missense_variant R123C 367C>T BRCA-US 16 3808953 3808953 single base substitution G A missense_variant R1053C 3157C>T BRCA-US 16 3808953 3808953 single base substitution G A missense_variant R1091C 3271C>T BRCA-US 16 3808953 3808953 single base substitution G A missense_variant R45C 133C>T BRCA-US 16 3823824 3823824 insertion of <=200bp - T exon_variant BRCA-US 16 3823824 3823824 insertion of <=200bp - T frameshift_variant N146N? BRCA-US 16 3823824 3823824 insertion of <=200bp - T frameshift_variant N219N? BRCA-US 16 3823824 3823824 insertion of <=200bp - T frameshift_variant N759N? BRCA-US 16 3823824 3823824 insertion of <=200bp - T frameshift_variant N797N? BRCA-US 16 3823824 3823824 insertion of <=200bp - T upstream_gene_variant BRCA-US 16 3827658 3827658 single base substitution T C intron_variant BRCA-US 16 3827658 3827658 single base substitution T C missense_variant N54S 161A>G BRCA-US 16 3827658 3827658 single base substitution T C missense_variant N667S 2000A>G BRCA-US 16 3827658 3827658 single base substitution T C missense_variant N705S 2114A>G BRCA-US 16 3827658 3827658 single base substitution T C upstream_gene_variant BRCA-US 16 3900518 3900518 single base substitution G C missense_variant S193C 578C>G BRCA-US 16 3900736 3900736 single base substitution C T synonymous_variant K120K 360G>A BTCA-JP 16 3779453 3779453 single base substitution C T downstream_gene_variant BTCA-JP 16 3779453 3779453 single base substitution C T missense_variant M1827I 5481G>A BTCA-JP 16 3779453 3779453 single base substitution C T missense_variant M1865I 5595G>A BTCA-JP 16 3779578 3779578 single base substitution C T downstream_gene_variant BTCA-JP 16 3779578 3779578 single base substitution C T missense_variant A1786T 5356G>A BTCA-JP 16 3779578 3779578 single base substitution C T missense_variant A1824T 5470G>A BTCA-JP 16 3823712 3823712 single base substitution T A 3_prime_UTR_variant BTCA-JP 16 3823712 3823712 single base substitution T A downstream_gene_variant BTCA-JP 16 3823712 3823712 single base substitution T A intron_variant BTCA-JP 16 3823712 3823712 single base substitution T A upstream_gene_variant BTCA-JP 16 3828862 3828862 deletion of <=200bp T - intron_variant BTCA-JP 16 3828862 3828862 deletion of <=200bp T - upstream_gene_variant BTCA-JP 16 3842114 3842114 single base substitution C T intron_variant BTCA-JP 16 3843454 3843454 single base substitution C T synonymous_variant P383P 1149G>A BTCA-JP 16 3843525 3843525 single base substitution G C missense_variant L360V 1078C>G BTCA-JP 16 3843551 3843551 single base substitution C A missense_variant R351L 1052G>T BTCA-JP 16 3900680 3900680 single base substitution C T missense_variant S139N 416G>A BTCA-JP 16 3929765 3929765 single base substitution G C intron_variant CESC-US 16 3778628 3778628 single base substitution C T downstream_gene_variant CESC-US 16 3778628 3778628 single base substitution C T synonymous_variant Q2102Q 6306G>A CESC-US 16 3778628 3778628 single base substitution C T synonymous_variant Q2140Q 6420G>A CESC-US 16 3779771 3779771 single base substitution T A downstream_gene_variant CESC-US 16 3779771 3779771 single base substitution T A synonymous_variant P1721P 5163A>T CESC-US 16 3779771 3779771 single base substitution T A synonymous_variant P1759P 5277A>T CESC-US 16 3781798 3781798 single base substitution G T downstream_gene_variant CESC-US 16 3781798 3781798 single base substitution G T synonymous_variant A1585A 4755C>A CESC-US 16 3781798 3781798 single base substitution G T synonymous_variant A1623A 4869C>A CESC-US 16 3786138 3786138 single base substitution C G downstream_gene_variant CESC-US 16 3786138 3786138 single base substitution C G exon_variant CESC-US 16 3786138 3786138 single base substitution C G missense_variant D1505H 4513G>C CESC-US 16 3786138 3786138 single base substitution C G missense_variant D1543H 4627G>C CESC-US 16 3786748 3786748 single base substitution G C downstream_gene_variant CESC-US 16 3786748 3786748 single base substitution G C exon_variant CESC-US 16 3786748 3786748 single base substitution G C missense_variant P1450R 4349C>G CESC-US 16 3786748 3786748 single base substitution G C missense_variant P1488R 4463C>G CESC-US 16 3786798 3786798 single base substitution G C downstream_gene_variant CESC-US 16 3786798 3786798 single base substitution G C exon_variant CESC-US 16 3786798 3786798 single base substitution G C missense_variant I1433M 4299C>G CESC-US 16 3786798 3786798 single base substitution G C missense_variant I1471M 4413C>G CESC-US 16 3788618 3788618 single base substitution G A downstream_gene_variant CESC-US 16 3788618 3788618 single base substitution G A intron_variant CESC-US 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T CESC-US 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T CESC-US 16 3788618 3788618 single base substitution G A upstream_gene_variant CESC-US 16 3794922 3794922 single base substitution G A exon_variant CESC-US 16 3794922 3794922 single base substitution G A stop_gained R1281* 3841C>T CESC-US 16 3794922 3794922 single base substitution G A stop_gained R1319* 3955C>T CESC-US 16 3794922 3794922 single base substitution G A stop_gained R192* 574C>T CESC-US 16 3794922 3794922 single base substitution G A stop_gained R87* 259C>T CESC-US 16 3794922 3794922 single base substitution G A upstream_gene_variant CESC-US 16 3799625 3799625 insertion of <=200bp - A splice_region_variant CESC-US 16 3799625 3799625 insertion of <=200bp - A upstream_gene_variant CESC-US 16 3801726 3801726 single base substitution C T intron_variant CESC-US 16 3801726 3801726 single base substitution C T splice_donor_variant CESC-US 16 3817784 3817784 single base substitution C A exon_variant CESC-US 16 3817784 3817784 single base substitution C A stop_gained E1025* 3073G>T CESC-US 16 3817784 3817784 single base substitution C A stop_gained E1063* 3187G>T CESC-US 16 3817784 3817784 single base substitution C A stop_gained E17* 49G>T CESC-US 16 3817799 3817799 single base substitution C A exon_variant CESC-US 16 3817799 3817799 single base substitution C A stop_gained E1020* 3058G>T CESC-US 16 3817799 3817799 single base substitution C A stop_gained E1058* 3172G>T CESC-US 16 3817799 3817799 single base substitution C A stop_gained E12* 34G>T CESC-US 16 3900422 3900422 single base substitution G A missense_variant P225L 674C>T CESC-US 16 3900459 3900459 single base substitution G A missense_variant L213F 637C>T CESC-US 16 3900710 3900710 single base substitution G A missense_variant S129L 386C>T CESC-US 16 3900710 3900710 single base substitution G T stop_gained S129* 386C>A CESC-US 16 3900884 3900884 single base substitution G A missense_variant S71L 212C>T CESC-US 16 3900914 3900914 single base substitution G A missense_variant P61L 182C>T CESC-US 16 3901001 3901001 single base substitution G A missense_variant S32L 95C>T CLLE-ES 16 3786166 3786166 single base substitution A G downstream_gene_variant CLLE-ES 16 3786166 3786166 single base substitution A G exon_variant CLLE-ES 16 3786166 3786166 single base substitution A G synonymous_variant S1495S 4485T>C CLLE-ES 16 3786166 3786166 single base substitution A G synonymous_variant S1533S 4599T>C CLLE-ES 16 3792434 3792434 single base substitution T C exon_variant CLLE-ES 16 3792434 3792434 single base substitution T C intron_variant CLLE-ES 16 3817724 3817724 single base substitution T A exon_variant CLLE-ES 16 3817724 3817724 single base substitution T A stop_gained K1045* 3133A>T CLLE-ES 16 3817724 3817724 single base substitution T A stop_gained K1083* 3247A>T CLLE-ES 16 3817724 3817724 single base substitution T A stop_gained K37* 109A>T CLLE-ES 16 3821321 3821321 single base substitution C T downstream_gene_variant CLLE-ES 16 3821321 3821321 single base substitution C T intron_variant CLLE-ES 16 3821321 3821321 single base substitution C T upstream_gene_variant CLLE-ES 16 3831615 3831615 single base substitution A G intron_variant CLLE-ES 16 3831615 3831615 single base substitution A G upstream_gene_variant CLLE-ES 16 3836066 3836066 single base substitution G A intron_variant CLLE-ES 16 3845668 3845668 single base substitution A C intron_variant CLLE-ES 16 3921232 3921232 single base substitution A C intron_variant CLLE-ES 16 3930763 3930763 single base substitution G A upstream_gene_variant COAD-US 16 3777817 3777817 deletion of <=200bp G - downstream_gene_variant COAD-US 16 3777817 3777817 deletion of <=200bp G - frameshift_variant Q2373 COAD-US 16 3777817 3777817 deletion of <=200bp G - frameshift_variant Q2411 COAD-US 16 3778452 3778452 single base substitution T A downstream_gene_variant COAD-US 16 3778452 3778452 single base substitution T A missense_variant Q2161L 6482A>T COAD-US 16 3778452 3778452 single base substitution T A missense_variant Q2199L 6596A>T COAD-US 16 3778976 3778976 single base substitution C T downstream_gene_variant COAD-US 16 3778976 3778976 single base substitution C T synonymous_variant A1986A 5958G>A COAD-US 16 3778976 3778976 single base substitution C T synonymous_variant A2024A 6072G>A COAD-US 16 3779252 3779252 single base substitution C A downstream_gene_variant COAD-US 16 3779252 3779252 single base substitution C A synonymous_variant T1894T 5682G>T COAD-US 16 3779252 3779252 single base substitution C A synonymous_variant T1932T 5796G>T COAD-US 16 3779278 3779278 single base substitution C T downstream_gene_variant COAD-US 16 3779278 3779278 single base substitution C T missense_variant V1886M 5656G>A COAD-US 16 3779278 3779278 single base substitution C T missense_variant V1924M 5770G>A COAD-US 16 3779692 3779692 single base substitution G A downstream_gene_variant COAD-US 16 3779692 3779692 single base substitution G A missense_variant R1748C 5242C>T COAD-US 16 3779692 3779692 single base substitution G A missense_variant R1786C 5356C>T COAD-US 16 3779844 3779844 single base substitution G A downstream_gene_variant COAD-US 16 3779844 3779844 single base substitution G A missense_variant T1697M 5090C>T COAD-US 16 3779844 3779844 single base substitution G A missense_variant T1735M 5204C>T COAD-US 16 3781301 3781301 single base substitution C T downstream_gene_variant COAD-US 16 3781301 3781301 single base substitution C T synonymous_variant T1650T 4950G>A COAD-US 16 3781301 3781301 single base substitution C T synonymous_variant T1688T 5064G>A COAD-US 16 3788618 3788618 single base substitution G A downstream_gene_variant COAD-US 16 3788618 3788618 single base substitution G A intron_variant COAD-US 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T COAD-US 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T COAD-US 16 3788618 3788618 single base substitution G A upstream_gene_variant COAD-US 16 3789646 3789646 single base substitution C T downstream_gene_variant COAD-US 16 3789646 3789646 single base substitution C T exon_variant COAD-US 16 3789646 3789646 single base substitution C T intron_variant COAD-US 16 3789646 3789646 single base substitution C T missense_variant V1367M 4099G>A COAD-US 16 3789646 3789646 single base substitution C T missense_variant V1405M 4213G>A COAD-US 16 3789646 3789646 single base substitution C T missense_variant V173M 517G>A COAD-US 16 3789646 3789646 single base substitution C T missense_variant V278M 832G>A COAD-US 16 3789646 3789646 single base substitution C T upstream_gene_variant COAD-US 16 3795310 3795310 single base substitution G A exon_variant COAD-US 16 3795310 3795310 single base substitution G A synonymous_variant C1256C 3768C>T COAD-US 16 3795310 3795310 single base substitution G A synonymous_variant C1294C 3882C>T COAD-US 16 3795310 3795310 single base substitution G A synonymous_variant C167C 501C>T COAD-US 16 3795310 3795310 single base substitution G A synonymous_variant C62C 186C>T COAD-US 16 3795310 3795310 single base substitution G A upstream_gene_variant COAD-US 16 3807912 3807912 single base substitution G A synonymous_variant R1131R 3393C>T COAD-US 16 3807912 3807912 single base substitution G A synonymous_variant R1169R 3507C>T COAD-US 16 3807912 3807912 single base substitution G A synonymous_variant R123R 369C>T COAD-US 16 3807914 3807914 single base substitution G A missense_variant R1131C 3391C>T COAD-US 16 3807914 3807914 single base substitution G A missense_variant R1169C 3505C>T COAD-US 16 3807914 3807914 single base substitution G A missense_variant R123C 367C>T COAD-US 16 3807926 3807926 single base substitution A G missense_variant W1127R 3379T>C COAD-US 16 3807926 3807926 single base substitution A G missense_variant W1165R 3493T>C COAD-US 16 3807926 3807926 single base substitution A G missense_variant W119R 355T>C COAD-US 16 3817720 3817720 insertion of <=200bp - T exon_variant COAD-US 16 3817720 3817720 insertion of <=200bp - T splice_donor_variant COAD-US 16 3820934 3820934 single base substitution C A downstream_gene_variant COAD-US 16 3820934 3820934 single base substitution C A missense_variant Q801H 2403G>T COAD-US 16 3820934 3820934 single base substitution C A missense_variant Q839H 2517G>T COAD-US 16 3820934 3820934 single base substitution C A upstream_gene_variant COAD-US 16 3828184 3828184 single base substitution C A splice_acceptor_variant COAD-US 16 3828184 3828184 single base substitution C A upstream_gene_variant COAD-US 16 3830755 3830755 single base substitution G A missense_variant R38W 112C>T COAD-US 16 3830755 3830755 single base substitution G A missense_variant R563W 1687C>T COAD-US 16 3830755 3830755 single base substitution G A missense_variant R601W 1801C>T COAD-US 16 3830755 3830755 single base substitution G A upstream_gene_variant COAD-US 16 3842083 3842083 single base substitution G A intron_variant COAD-US 16 3842083 3842083 single base substitution G A missense_variant A410V 1229C>T COAD-US 16 3900740 3900740 single base substitution C A missense_variant G119V 356G>T COCA-CN 16 3778025 3778025 single base substitution G T downstream_gene_variant COCA-CN 16 3778025 3778025 single base substitution G T missense_variant N2303K 6909C>A COCA-CN 16 3778025 3778025 single base substitution G T missense_variant N2341K 7023C>A COCA-CN 16 3781374 3781374 single base substitution C T downstream_gene_variant COCA-CN 16 3781374 3781374 single base substitution C T missense_variant R1626H 4877G>A COCA-CN 16 3781374 3781374 single base substitution C T missense_variant R1664H 4991G>A COCA-CN 16 3788637 3788637 single base substitution G T downstream_gene_variant COCA-CN 16 3788637 3788637 single base substitution G T intron_variant COCA-CN 16 3788637 3788637 single base substitution G T missense_variant F1401L 4203C>A COCA-CN 16 3788637 3788637 single base substitution G T missense_variant F1439L 4317C>A COCA-CN 16 3788637 3788637 single base substitution G T upstream_gene_variant COCA-CN 16 3789537 3789537 single base substitution G A 3_prime_UTR_variant COCA-CN 16 3789537 3789537 single base substitution G A downstream_gene_variant COCA-CN 16 3789537 3789537 single base substitution G A intron_variant COCA-CN 16 3789537 3789537 single base substitution G A upstream_gene_variant COCA-CN 16 3817907 3817907 single base substitution T C exon_variant COCA-CN 16 3817907 3817907 single base substitution T C missense_variant M1022V 3064A>G COCA-CN 16 3817907 3817907 single base substitution T C missense_variant M984V 2950A>G COCA-CN 16 3817907 3817907 single base substitution T C upstream_gene_variant COCA-CN 16 3821133 3821133 single base substitution G A downstream_gene_variant COCA-CN 16 3821133 3821133 single base substitution G A intron_variant COCA-CN 16 3821133 3821133 single base substitution G A upstream_gene_variant COCA-CN 16 3821820 3821820 single base substitution T A downstream_gene_variant COCA-CN 16 3821820 3821820 single base substitution T A intron_variant COCA-CN 16 3821820 3821820 single base substitution T A upstream_gene_variant COCA-CN 16 3824547 3824547 single base substitution G T intron_variant COCA-CN 16 3824547 3824547 single base substitution G T upstream_gene_variant COCA-CN 16 3824704 3824704 single base substitution T C exon_variant COCA-CN 16 3824704 3824704 single base substitution T C intron_variant COCA-CN 16 3824704 3824704 single base substitution T C upstream_gene_variant COCA-CN 16 3827744 3827744 single base substitution G A intron_variant COCA-CN 16 3827744 3827744 single base substitution G A upstream_gene_variant COCA-CN 16 3841914 3841914 single base substitution C A intron_variant EOPC-DE 16 3903527 3903527 single base substitution C T intron_variant EOPC-DE 16 3921517 3921517 single base substitution G T intron_variant ESAD-UK 16 3770055 3770055 single base substitution T C downstream_gene_variant ESAD-UK 16 3770572 3770572 single base substitution G A downstream_gene_variant ESAD-UK 16 3772217 3772217 single base substitution C T downstream_gene_variant ESAD-UK 16 3772593 3772593 single base substitution T A downstream_gene_variant ESAD-UK 16 3774765 3774765 single base substitution C T downstream_gene_variant ESAD-UK 16 3782056 3782056 single base substitution C A downstream_gene_variant ESAD-UK 16 3782056 3782056 single base substitution C A intron_variant ESAD-UK 16 3782570 3782570 insertion of <=200bp - T downstream_gene_variant ESAD-UK 16 3782570 3782570 insertion of <=200bp - T intron_variant ESAD-UK 16 3788302 3788302 single base substitution G A downstream_gene_variant ESAD-UK 16 3788302 3788302 single base substitution G A intron_variant ESAD-UK 16 3788302 3788302 single base substitution G A upstream_gene_variant ESAD-UK 16 3789745 3789745 single base substitution C T downstream_gene_variant ESAD-UK 16 3789745 3789745 single base substitution C T intron_variant ESAD-UK 16 3789745 3789745 single base substitution C T upstream_gene_variant ESAD-UK 16 3790001 3790001 single base substitution C T downstream_gene_variant ESAD-UK 16 3790001 3790001 single base substitution C T intron_variant ESAD-UK 16 3790001 3790001 single base substitution C T upstream_gene_variant ESAD-UK 16 3791236 3791236 single base substitution G C exon_variant ESAD-UK 16 3791236 3791236 single base substitution G C intron_variant ESAD-UK 16 3791236 3791236 single base substitution G C upstream_gene_variant ESAD-UK 16 3794761 3794761 single base substitution G A intron_variant ESAD-UK 16 3794761 3794761 single base substitution G A upstream_gene_variant ESAD-UK 16 3795984 3795984 single base substitution C A intron_variant ESAD-UK 16 3795984 3795984 single base substitution C A upstream_gene_variant ESAD-UK 16 3796008 3796008 single base substitution C T intron_variant ESAD-UK 16 3796008 3796008 single base substitution C T upstream_gene_variant ESAD-UK 16 3799102 3799102 single base substitution C G intron_variant ESAD-UK 16 3799102 3799102 single base substitution C G upstream_gene_variant ESAD-UK 16 3799627 3799627 single base substitution C T splice_donor_variant ESAD-UK 16 3799627 3799627 single base substitution C T upstream_gene_variant ESAD-UK 16 3800870 3800870 single base substitution G A intron_variant ESAD-UK 16 3801419 3801419 single base substitution C T intron_variant ESAD-UK 16 3801777 3801777 single base substitution C T intron_variant ESAD-UK 16 3801777 3801777 single base substitution C T synonymous_variant E11E 33G>A ESAD-UK 16 3801777 3801777 single base substitution C T synonymous_variant E1205E 3615G>A ESAD-UK 16 3801777 3801777 single base substitution C T synonymous_variant E1243E 3729G>A ESAD-UK 16 3803893 3803893 single base substitution G A intron_variant ESAD-UK 16 3803893 3803893 single base substitution G A upstream_gene_variant ESAD-UK 16 3806205 3806205 single base substitution G C intron_variant ESAD-UK 16 3806205 3806205 single base substitution G C upstream_gene_variant ESAD-UK 16 3806602 3806602 single base substitution G T intron_variant ESAD-UK 16 3806602 3806602 single base substitution G T upstream_gene_variant ESAD-UK 16 3806851 3806851 single base substitution G A intron_variant ESAD-UK 16 3806943 3806943 single base substitution C G intron_variant ESAD-UK 16 3807154 3807154 single base substitution C T intron_variant ESAD-UK 16 3813240 3813240 single base substitution T G downstream_gene_variant ESAD-UK 16 3813240 3813240 single base substitution T G intron_variant ESAD-UK 16 3814145 3814145 deletion of <=200bp T - downstream_gene_variant ESAD-UK 16 3814145 3814145 deletion of <=200bp T - intron_variant ESAD-UK 16 3814759 3814759 insertion of <=200bp - T downstream_gene_variant ESAD-UK 16 3814759 3814759 insertion of <=200bp - T intron_variant ESAD-UK 16 3817721 3817721 insertion of <=200bp - T exon_variant ESAD-UK 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I1046N? ESAD-UK 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I1084N? ESAD-UK 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I38N? ESAD-UK 16 3818332 3818332 single base substitution G A intron_variant ESAD-UK 16 3818332 3818332 single base substitution G A upstream_gene_variant ESAD-UK 16 3820494 3820494 single base substitution G A downstream_gene_variant ESAD-UK 16 3820494 3820494 single base substitution G A intron_variant ESAD-UK 16 3820494 3820494 single base substitution G A upstream_gene_variant ESAD-UK 16 3826233 3826233 single base substitution C A intron_variant ESAD-UK 16 3826233 3826233 single base substitution C A upstream_gene_variant ESAD-UK 16 3826383 3826383 single base substitution T C intron_variant ESAD-UK 16 3826383 3826383 single base substitution T C upstream_gene_variant ESAD-UK 16 3830747 3830752 deletion of <=200bp ATGGCT - inframe_deletion SH39 ESAD-UK 16 3830747 3830752 deletion of <=200bp ATGGCT - inframe_deletion SH564 ESAD-UK 16 3830747 3830752 deletion of <=200bp ATGGCT - inframe_deletion SH602 ESAD-UK 16 3830747 3830752 deletion of <=200bp ATGGCT - upstream_gene_variant ESAD-UK 16 3830755 3830757 deletion of <=200bp GCA - disruptive_inframe_deletion LR37R ESAD-UK 16 3830755 3830757 deletion of <=200bp GCA - disruptive_inframe_deletion LR562R ESAD-UK 16 3830755 3830757 deletion of <=200bp GCA - disruptive_inframe_deletion LR600R ESAD-UK 16 3830755 3830757 deletion of <=200bp GCA - upstream_gene_variant ESAD-UK 16 3830764 3830766 deletion of <=200bp GAG - disruptive_inframe_deletion TQ34K ESAD-UK 16 3830764 3830766 deletion of <=200bp GAG - disruptive_inframe_deletion TQ559K ESAD-UK 16 3830764 3830766 deletion of <=200bp GAG - disruptive_inframe_deletion TQ597K ESAD-UK 16 3830764 3830766 deletion of <=200bp GAG - upstream_gene_variant ESAD-UK 16 3830768 3830768 deletion of <=200bp G - frameshift_variant V33 ESAD-UK 16 3830768 3830768 deletion of <=200bp G - frameshift_variant V558 ESAD-UK 16 3830768 3830768 deletion of <=200bp G - frameshift_variant V596 ESAD-UK 16 3830768 3830768 deletion of <=200bp G - upstream_gene_variant ESAD-UK 16 3830772 3830774 deletion of <=200bp TGT - disruptive_inframe_deletion EH31D ESAD-UK 16 3830772 3830774 deletion of <=200bp TGT - disruptive_inframe_deletion EH556D ESAD-UK 16 3830772 3830774 deletion of <=200bp TGT - disruptive_inframe_deletion EH594D ESAD-UK 16 3830772 3830774 deletion of <=200bp TGT - upstream_gene_variant ESAD-UK 16 3830853 3830853 single base substitution G C missense_variant S530C 1589C>G ESAD-UK 16 3830853 3830853 single base substitution G C missense_variant S568C 1703C>G ESAD-UK 16 3830853 3830853 single base substitution G C missense_variant S5C 14C>G ESAD-UK 16 3830853 3830853 single base substitution G C upstream_gene_variant ESAD-UK 16 3830982 3830982 single base substitution A T intron_variant ESAD-UK 16 3830982 3830982 single base substitution A T upstream_gene_variant ESAD-UK 16 3833707 3833707 single base substitution C A intron_variant ESAD-UK 16 3833707 3833707 single base substitution C A upstream_gene_variant ESAD-UK 16 3837927 3837927 single base substitution A C intron_variant ESAD-UK 16 3837928 3837928 single base substitution C T intron_variant ESAD-UK 16 3838576 3838576 single base substitution T C intron_variant ESAD-UK 16 3839052 3839052 single base substitution A G intron_variant ESAD-UK 16 3839461 3839461 single base substitution A T intron_variant ESAD-UK 16 3842019 3842019 single base substitution G A intron_variant ESAD-UK 16 3842019 3842019 single base substitution G A synonymous_variant L431L 1293C>T ESAD-UK 16 3843670 3843670 single base substitution G A intron_variant ESAD-UK 16 3847390 3847390 single base substitution C A intron_variant ESAD-UK 16 3847838 3847838 single base substitution T A intron_variant ESAD-UK 16 3849149 3849149 single base substitution G A intron_variant ESAD-UK 16 3850495 3850495 single base substitution T A intron_variant ESAD-UK 16 3850677 3850677 single base substitution G T intron_variant ESAD-UK 16 3851157 3851157 single base substitution G C intron_variant ESAD-UK 16 3853167 3853167 single base substitution T A intron_variant ESAD-UK 16 3853168 3853168 insertion of <=200bp - A intron_variant ESAD-UK 16 3853168 3853168 single base substitution A T intron_variant ESAD-UK 16 3854837 3854837 single base substitution T A intron_variant ESAD-UK 16 3856730 3856730 single base substitution C T intron_variant ESAD-UK 16 3857129 3857129 single base substitution C T intron_variant ESAD-UK 16 3858117 3858117 single base substitution G C intron_variant ESAD-UK 16 3859148 3859148 single base substitution G C intron_variant ESAD-UK 16 3863318 3863318 single base substitution C T intron_variant ESAD-UK 16 3864051 3864051 single base substitution C A intron_variant ESAD-UK 16 3869061 3869061 single base substitution C T intron_variant ESAD-UK 16 3870266 3870266 single base substitution C G intron_variant ESAD-UK 16 3870496 3870496 single base substitution G T intron_variant ESAD-UK 16 3871037 3871037 single base substitution C T intron_variant ESAD-UK 16 3872552 3872552 single base substitution G A intron_variant ESAD-UK 16 3875479 3875479 single base substitution T G intron_variant ESAD-UK 16 3881507 3881507 single base substitution C T intron_variant ESAD-UK 16 3885526 3885526 single base substitution C T intron_variant ESAD-UK 16 3887344 3887344 single base substitution C T intron_variant ESAD-UK 16 3887657 3887657 single base substitution T A intron_variant ESAD-UK 16 3888733 3888733 single base substitution T G intron_variant ESAD-UK 16 3891664 3891664 single base substitution G A intron_variant ESAD-UK 16 3892575 3892575 single base substitution A T intron_variant ESAD-UK 16 3897502 3897502 deletion of <=200bp A - intron_variant ESAD-UK 16 3898960 3898960 single base substitution G A intron_variant ESAD-UK 16 3902825 3902825 single base substitution T A intron_variant ESAD-UK 16 3909673 3909673 single base substitution G A intron_variant ESAD-UK 16 3910347 3910347 deletion of <=200bp T - intron_variant ESAD-UK 16 3912480 3912480 single base substitution A T intron_variant ESAD-UK 16 3914412 3914412 single base substitution G A intron_variant ESAD-UK 16 3915071 3915071 single base substitution G T intron_variant ESAD-UK 16 3916723 3916723 single base substitution C T intron_variant ESAD-UK 16 3917035 3917035 single base substitution A C intron_variant ESAD-UK 16 3918555 3918555 single base substitution A C intron_variant ESAD-UK 16 3923579 3923579 single base substitution C T intron_variant ESAD-UK 16 3931014 3931014 single base substitution G T upstream_gene_variant ESAD-UK 16 3932326 3932326 single base substitution T G upstream_gene_variant ESCA-CN 16 3778714 3778714 single base substitution G C downstream_gene_variant ESCA-CN 16 3778714 3778714 single base substitution G C missense_variant Q2074E 6220C>G ESCA-CN 16 3778714 3778714 single base substitution G C missense_variant Q2112E 6334C>G ESCA-CN 16 3779388 3779388 single base substitution G C downstream_gene_variant ESCA-CN 16 3779388 3779388 single base substitution G C stop_gained S1849* 5546C>G ESCA-CN 16 3779388 3779388 single base substitution G C stop_gained S1887* 5660C>G ESCA-CN 16 3779662 3779662 single base substitution G A downstream_gene_variant ESCA-CN 16 3779662 3779662 single base substitution G A stop_gained Q1758* 5272C>T ESCA-CN 16 3779662 3779662 single base substitution G A stop_gained Q1796* 5386C>T ESCA-CN 16 3781336 3781336 single base substitution C T downstream_gene_variant ESCA-CN 16 3781336 3781336 single base substitution C T missense_variant E1639K 4915G>A ESCA-CN 16 3781336 3781336 single base substitution C T missense_variant E1677K 5029G>A ESCA-CN 16 3781793 3781793 single base substitution A G downstream_gene_variant ESCA-CN 16 3781793 3781793 single base substitution A G missense_variant M1587T 4760T>C ESCA-CN 16 3781793 3781793 single base substitution A G missense_variant M1625T 4874T>C ESCA-CN 16 3786197 3786197 deletion of <=200bp A - downstream_gene_variant ESCA-CN 16 3786197 3786197 deletion of <=200bp A - exon_variant ESCA-CN 16 3786197 3786197 deletion of <=200bp A - frameshift_variant F1485 ESCA-CN 16 3786197 3786197 deletion of <=200bp A - frameshift_variant F1523 ESCA-CN 16 3788651 3788651 single base substitution C G downstream_gene_variant ESCA-CN 16 3788651 3788651 single base substitution C G intron_variant ESCA-CN 16 3788651 3788651 single base substitution C G missense_variant D1397H 4189G>C ESCA-CN 16 3788651 3788651 single base substitution C G missense_variant D1435H 4303G>C ESCA-CN 16 3788651 3788651 single base substitution C G upstream_gene_variant ESCA-CN 16 3795292 3795292 single base substitution G T exon_variant ESCA-CN 16 3795292 3795292 single base substitution G T synonymous_variant I1262I 3786C>A ESCA-CN 16 3795292 3795292 single base substitution G T synonymous_variant I1300I 3900C>A ESCA-CN 16 3795292 3795292 single base substitution G T synonymous_variant I173I 519C>A ESCA-CN 16 3795292 3795292 single base substitution G T synonymous_variant I68I 204C>A ESCA-CN 16 3795292 3795292 single base substitution G T upstream_gene_variant ESCA-CN 16 3817754 3817754 single base substitution G C exon_variant ESCA-CN 16 3817754 3817754 single base substitution G C missense_variant Q1035E 3103C>G ESCA-CN 16 3817754 3817754 single base substitution G C missense_variant Q1073E 3217C>G ESCA-CN 16 3817754 3817754 single base substitution G C missense_variant Q27E 79C>G ESCA-CN 16 3828769 3828769 single base substitution G A missense_variant R587C 1759C>T ESCA-CN 16 3828769 3828769 single base substitution G A missense_variant R625C 1873C>T ESCA-CN 16 3828769 3828769 single base substitution G A missense_variant R62C 184C>T ESCA-CN 16 3828769 3828769 single base substitution G A upstream_gene_variant GBM-US 16 3779062 3779062 single base substitution C T downstream_gene_variant GBM-US 16 3779062 3779062 single base substitution C T missense_variant A1958T 5872G>A GBM-US 16 3779062 3779062 single base substitution C T missense_variant A1996T 5986G>A GBM-US 16 3790494 3790494 single base substitution G A exon_variant GBM-US 16 3790494 3790494 single base substitution G A missense_variant R115W 343C>T GBM-US 16 3790494 3790494 single base substitution G A missense_variant R1309W 3925C>T GBM-US 16 3790494 3790494 single base substitution G A missense_variant R1347W 4039C>T GBM-US 16 3790494 3790494 single base substitution G A missense_variant R220W 658C>T GBM-US 16 3790494 3790494 single base substitution G A upstream_gene_variant GBM-US 16 3807844 3807844 single base substitution A G intron_variant GBM-US 16 3807844 3807844 single base substitution A G missense_variant V1154A 3461T>C GBM-US 16 3807844 3807844 single base substitution A G missense_variant V1192A 3575T>C GBM-US 16 3820625 3820625 single base substitution A G downstream_gene_variant GBM-US 16 3820625 3820625 single base substitution A G exon_variant GBM-US 16 3820625 3820625 single base substitution A G synonymous_variant P904P 2712T>C GBM-US 16 3820625 3820625 single base substitution A G synonymous_variant P942P 2826T>C GBM-US 16 3820625 3820625 single base substitution A G upstream_gene_variant GBM-US 16 3842056 3842056 single base substitution C T intron_variant GBM-US 16 3842056 3842056 single base substitution C T stop_gained W419* 1256G>A GBM-US 16 3843446 3843446 deletion of <=200bp C - frameshift_variant R386 KIRC-US 16 3807365 3807365 single base substitution G T intron_variant KIRC-US 16 3807365 3807365 single base substitution G T missense_variant P1170T 3508C>A KIRC-US 16 3807365 3807365 single base substitution G T missense_variant P1208T 3622C>A KIRC-US 16 3820642 3820642 single base substitution G T downstream_gene_variant KIRC-US 16 3820642 3820642 single base substitution G T exon_variant KIRC-US 16 3820642 3820642 single base substitution G T missense_variant P899T 2695C>A KIRC-US 16 3820642 3820642 single base substitution G T missense_variant P937T 2809C>A KIRC-US 16 3820642 3820642 single base substitution G T upstream_gene_variant KIRC-US 16 3843626 3843626 single base substitution G A missense_variant S326F 977C>T KIRC-US 16 3860701 3860701 single base substitution A G missense_variant V293A 878T>C KIRP-US 16 3779018 3779018 single base substitution C T downstream_gene_variant KIRP-US 16 3779018 3779018 single base substitution C T synonymous_variant G1972G 5916G>A KIRP-US 16 3779018 3779018 single base substitution C T synonymous_variant G2010G 6030G>A KIRP-US 16 3807907 3807907 single base substitution G A missense_variant T1133I 3398C>T KIRP-US 16 3807907 3807907 single base substitution G A missense_variant T1171I 3512C>T KIRP-US 16 3807907 3807907 single base substitution G A missense_variant T125I 374C>T KIRP-US 16 3817823 3817823 single base substitution C A exon_variant KIRP-US 16 3817823 3817823 single base substitution C A stop_gained E1012* 3034G>T KIRP-US 16 3817823 3817823 single base substitution C A stop_gained E1050* 3148G>T KIRP-US 16 3817823 3817823 single base substitution C A stop_gained E4* 10G>T KIRP-US 16 3860637 3860637 single base substitution G A synonymous_variant I314I 942C>T KIRP-US 16 3901001 3901001 single base substitution G A missense_variant S32L 95C>T LAML-KR 16 3787470 3787470 single base substitution G T downstream_gene_variant LAML-KR 16 3787470 3787470 single base substitution G T intron_variant LAML-KR 16 3787470 3787470 single base substitution G T upstream_gene_variant LAML-KR 16 3791824 3791824 single base substitution T C exon_variant LAML-KR 16 3791824 3791824 single base substitution T C intron_variant LAML-KR 16 3791824 3791824 single base substitution T C upstream_gene_variant LAML-KR 16 3791831 3791831 single base substitution T C exon_variant LAML-KR 16 3791831 3791831 single base substitution T C intron_variant LAML-KR 16 3791831 3791831 single base substitution T C upstream_gene_variant LAML-KR 16 3809106 3809106 single base substitution T C intron_variant LAML-KR 16 3820667 3820667 single base substitution C T downstream_gene_variant LAML-KR 16 3820667 3820667 single base substitution C T exon_variant LAML-KR 16 3820667 3820667 single base substitution C T synonymous_variant P890P 2670G>A LAML-KR 16 3820667 3820667 single base substitution C T synonymous_variant P928P 2784G>A LAML-KR 16 3820667 3820667 single base substitution C T upstream_gene_variant LAML-KR 16 3826973 3826973 single base substitution C G intron_variant LAML-KR 16 3826973 3826973 single base substitution C G upstream_gene_variant LAML-KR 16 3827082 3827082 single base substitution T G intron_variant LAML-KR 16 3827082 3827082 single base substitution T G upstream_gene_variant LAML-KR 16 3827553 3827553 single base substitution G A intron_variant LAML-KR 16 3827553 3827553 single base substitution G A upstream_gene_variant LAML-KR 16 3827931 3827931 single base substitution T C intron_variant LAML-KR 16 3827931 3827931 single base substitution T C upstream_gene_variant LGG-US 16 3781317 3781317 single base substitution C G downstream_gene_variant LGG-US 16 3781317 3781317 single base substitution C G missense_variant R1645P 4934G>C LGG-US 16 3781317 3781317 single base substitution C G missense_variant R1683P 5048G>C LGG-US 16 3781375 3781375 single base substitution G A downstream_gene_variant LGG-US 16 3781375 3781375 single base substitution G A missense_variant R1626C 4876C>T LGG-US 16 3781375 3781375 single base substitution G A missense_variant R1664C 4990C>T LGG-US 16 3828795 3828795 deletion of <=200bp G - frameshift_variant P53 LGG-US 16 3828795 3828795 deletion of <=200bp G - frameshift_variant P578 LGG-US 16 3828795 3828795 deletion of <=200bp G - frameshift_variant P616 LGG-US 16 3828795 3828795 deletion of <=200bp G - upstream_gene_variant LGG-US 16 3832889 3832889 single base substitution T C missense_variant I419V 1255A>G LGG-US 16 3832889 3832889 single base substitution T C missense_variant I457V 1369A>G LGG-US 16 3832889 3832889 single base substitution T C upstream_gene_variant LICA-CN 16 3778278 3778278 single base substitution T A downstream_gene_variant LICA-CN 16 3778278 3778278 single base substitution T A missense_variant Q2219L 6656A>T LICA-CN 16 3778278 3778278 single base substitution T A missense_variant Q2257L 6770A>T LICA-CN 16 3828185 3828185 single base substitution T C splice_acceptor_variant LICA-CN 16 3828185 3828185 single base substitution T C upstream_gene_variant LICA-CN 16 3828727 3828727 single base substitution C A missense_variant D601Y 1801G>T LICA-CN 16 3828727 3828727 single base substitution C A missense_variant D639Y 1915G>T LICA-CN 16 3828727 3828727 single base substitution C A missense_variant D76Y 226G>T LICA-CN 16 3828727 3828727 single base substitution C A upstream_gene_variant LICA-CN 16 3900433 3900433 single base substitution T A synonymous_variant G221G 663A>T LICA-FR 16 3778756 3778756 single base substitution C T downstream_gene_variant LICA-FR 16 3778756 3778756 single base substitution C T missense_variant A2060T 6178G>A LICA-FR 16 3778756 3778756 single base substitution C T missense_variant A2098T 6292G>A LICA-FR 16 3779036 3779036 single base substitution T A downstream_gene_variant LICA-FR 16 3779036 3779036 single base substitution T A synonymous_variant R1966R 5898A>T LICA-FR 16 3779036 3779036 single base substitution T A synonymous_variant R2004R 6012A>T LICA-FR 16 3786797 3786797 single base substitution A T downstream_gene_variant LICA-FR 16 3786797 3786797 single base substitution A T exon_variant LICA-FR 16 3786797 3786797 single base substitution A T missense_variant W1434R 4300T>A LICA-FR 16 3786797 3786797 single base substitution A T missense_variant W1472R 4414T>A LICA-FR 16 3789646 3789646 single base substitution C G downstream_gene_variant LICA-FR 16 3789646 3789646 single base substitution C G exon_variant LICA-FR 16 3789646 3789646 single base substitution C G intron_variant LICA-FR 16 3789646 3789646 single base substitution C G missense_variant V1367L 4099G>C LICA-FR 16 3789646 3789646 single base substitution C G missense_variant V1405L 4213G>C LICA-FR 16 3789646 3789646 single base substitution C G missense_variant V173L 517G>C LICA-FR 16 3789646 3789646 single base substitution C G missense_variant V278L 832G>C LICA-FR 16 3789646 3789646 single base substitution C G upstream_gene_variant LICA-FR 16 3789702 3789702 single base substitution G C downstream_gene_variant LICA-FR 16 3789702 3789702 single base substitution G C exon_variant LICA-FR 16 3789702 3789702 single base substitution G C intron_variant LICA-FR 16 3789702 3789702 single base substitution G C missense_variant S1348C 4043C>G LICA-FR 16 3789702 3789702 single base substitution G C missense_variant S1386C 4157C>G LICA-FR 16 3789702 3789702 single base substitution G C missense_variant S154C 461C>G LICA-FR 16 3789702 3789702 single base substitution G C missense_variant S259C 776C>G LICA-FR 16 3789702 3789702 single base substitution G C upstream_gene_variant LICA-FR 16 3800634 3800634 single base substitution T C intron_variant LICA-FR 16 3800634 3800634 single base substitution T C upstream_gene_variant LICA-FR 16 3801787 3801787 single base substitution C T intron_variant LICA-FR 16 3801787 3801787 single base substitution C T missense_variant C1202Y 3605G>A LICA-FR 16 3801787 3801787 single base substitution C T missense_variant C1240Y 3719G>A LICA-FR 16 3801787 3801787 single base substitution C T missense_variant C8Y 23G>A LICA-FR 16 3814958 3814958 single base substitution T G downstream_gene_variant LICA-FR 16 3814958 3814958 single base substitution T G intron_variant LICA-FR 16 3819258 3819258 single base substitution G A downstream_gene_variant LICA-FR 16 3819258 3819258 single base substitution G A exon_variant LICA-FR 16 3819258 3819258 single base substitution G A missense_variant P955S 2863C>T LICA-FR 16 3819258 3819258 single base substitution G A missense_variant P993S 2977C>T LICA-FR 16 3819258 3819258 single base substitution G A upstream_gene_variant LICA-FR 16 3831261 3831261 single base substitution C A missense_variant Q502H 1506G>T LICA-FR 16 3831261 3831261 single base substitution C A missense_variant Q540H 1620G>T LICA-FR 16 3831261 3831261 single base substitution C A upstream_gene_variant LICA-FR 16 3848064 3848064 single base substitution C T intron_variant LICA-FR 16 3865552 3865552 single base substitution T A intron_variant LICA-FR 16 3874258 3874258 single base substitution G C intron_variant LICA-FR 16 3874678 3874678 single base substitution C G intron_variant LICA-FR 16 3895973 3895973 single base substitution C A intron_variant LICA-FR 16 3896596 3896596 single base substitution T C intron_variant LICA-FR 16 3900415 3900415 single base substitution A T synonymous_variant P227P 681T>A LICA-FR 16 3900595 3900595 single base substitution G A synonymous_variant A167A 501C>T LICA-FR 16 3917827 3917827 single base substitution G A intron_variant LICA-FR 16 3932488 3932488 deletion of <=200bp T - upstream_gene_variant LIHC-US 16 3778391 3778391 single base substitution G T downstream_gene_variant LIHC-US 16 3778391 3778391 single base substitution G T synonymous_variant A2181A 6543C>A LIHC-US 16 3778391 3778391 single base substitution G T synonymous_variant A2219A 6657C>A LIHC-US 16 3778620 3778620 single base substitution T C downstream_gene_variant LIHC-US 16 3778620 3778620 single base substitution T C missense_variant N2105S 6314A>G LIHC-US 16 3778620 3778620 single base substitution T C missense_variant N2143S 6428A>G LIHC-US 16 3801728 3801728 single base substitution T C intron_variant LIHC-US 16 3801728 3801728 single base substitution T C missense_variant T1222A 3664A>G LIHC-US 16 3801728 3801728 single base substitution T C missense_variant T1260A 3778A>G LIHC-US 16 3801728 3801728 single base substitution T C missense_variant T28A 82A>G LIHC-US 16 3807292 3807292 single base substitution T C intron_variant LIHC-US 16 3807292 3807292 single base substitution T C missense_variant N1194S 3581A>G LIHC-US 16 3807292 3807292 single base substitution T C missense_variant N1232S 3695A>G LIHC-US 16 3817806 3817806 single base substitution C T exon_variant LIHC-US 16 3817806 3817806 single base substitution C T synonymous_variant V1017V 3051G>A LIHC-US 16 3817806 3817806 single base substitution C T synonymous_variant V1055V 3165G>A LIHC-US 16 3817806 3817806 single base substitution C T synonymous_variant V9V 27G>A LIHC-US 16 3820965 3820965 single base substitution A G downstream_gene_variant LIHC-US 16 3820965 3820965 single base substitution A G missense_variant L791P 2372T>C LIHC-US 16 3820965 3820965 single base substitution A G missense_variant L829P 2486T>C LIHC-US 16 3820965 3820965 single base substitution A G upstream_gene_variant LIHC-US 16 3830772 3830772 single base substitution T C missense_variant H32R 95A>G LIHC-US 16 3830772 3830772 single base substitution T C missense_variant H557R 1670A>G LIHC-US 16 3830772 3830772 single base substitution T C missense_variant H595R 1784A>G LIHC-US 16 3830772 3830772 single base substitution T C upstream_gene_variant LIHC-US 16 3860606 3860606 single base substitution T A missense_variant M325L 973A>T LINC-JP 16 3781159 3781159 single base substitution C T downstream_gene_variant LINC-JP 16 3781159 3781159 single base substitution C T intron_variant LINC-JP 16 3781501 3781501 single base substitution C A downstream_gene_variant LINC-JP 16 3781501 3781501 single base substitution C A intron_variant LINC-JP 16 3786705 3786705 single base substitution C A downstream_gene_variant LINC-JP 16 3786705 3786705 single base substitution C A exon_variant LINC-JP 16 3786705 3786705 single base substitution C A missense_variant W1464C 4392G>T LINC-JP 16 3786705 3786705 single base substitution C A missense_variant W1502C 4506G>T LINC-JP 16 3786849 3786849 single base substitution G A downstream_gene_variant LINC-JP 16 3786849 3786849 single base substitution G A exon_variant LINC-JP 16 3786849 3786849 single base substitution G A intron_variant LINC-JP 16 3788618 3788618 single base substitution G A downstream_gene_variant LINC-JP 16 3788618 3788618 single base substitution G A intron_variant LINC-JP 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T LINC-JP 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T LINC-JP 16 3788618 3788618 single base substitution G A upstream_gene_variant LINC-JP 16 3798869 3798869 single base substitution G T intron_variant LINC-JP 16 3798869 3798869 single base substitution G T upstream_gene_variant LINC-JP 16 3799627 3799627 single base substitution C T splice_donor_variant LINC-JP 16 3799627 3799627 single base substitution C T upstream_gene_variant LINC-JP 16 3802019 3802019 single base substitution A C intron_variant LINC-JP 16 3802019 3802019 single base substitution A C upstream_gene_variant LINC-JP 16 3807402 3807402 single base substitution T C intron_variant LINC-JP 16 3815313 3815313 single base substitution T A downstream_gene_variant LINC-JP 16 3815313 3815313 single base substitution T A intron_variant LINC-JP 16 3816032 3816032 single base substitution T C downstream_gene_variant LINC-JP 16 3816032 3816032 single base substitution T C intron_variant LINC-JP 16 3823936 3823936 single base substitution G C intron_variant LINC-JP 16 3823936 3823936 single base substitution G C splice_region_variant LINC-JP 16 3823936 3823936 single base substitution G C upstream_gene_variant LINC-JP 16 3825562 3825562 insertion of <=200bp - A intron_variant LINC-JP 16 3825562 3825562 insertion of <=200bp - A upstream_gene_variant LINC-JP 16 3827592 3827592 single base substitution T C intron_variant LINC-JP 16 3827592 3827592 single base substitution T C upstream_gene_variant LINC-JP 16 3832798 3832798 single base substitution G T missense_variant A449D 1346C>A LINC-JP 16 3832798 3832798 single base substitution G T missense_variant A487D 1460C>A LINC-JP 16 3832798 3832798 single base substitution G T upstream_gene_variant LINC-JP 16 3856470 3856470 single base substitution T A intron_variant LINC-JP 16 3856471 3856471 single base substitution C A intron_variant LINC-JP 16 3860518 3860518 single base substitution T C intron_variant LINC-JP 16 3860862 3860862 single base substitution C T intron_variant LINC-JP 16 3875759 3875759 single base substitution T C intron_variant LINC-JP 16 3883644 3883644 single base substitution T C intron_variant LINC-JP 16 3894578 3894578 single base substitution T C intron_variant LINC-JP 16 3896480 3896480 single base substitution C T intron_variant LINC-JP 16 3900862 3900862 single base substitution G A synonymous_variant S78S 234C>T LINC-JP 16 3929207 3929207 single base substitution G T intron_variant LINC-JP 16 3933490 3933490 insertion of <=200bp - A upstream_gene_variant LIRI-JP 16 3770209 3770209 single base substitution G C downstream_gene_variant LIRI-JP 16 3770434 3770434 single base substitution T C downstream_gene_variant LIRI-JP 16 3770914 3770916 deletion of <=200bp CTT - downstream_gene_variant LIRI-JP 16 3774797 3774797 single base substitution C T downstream_gene_variant LIRI-JP 16 3776721 3776721 single base substitution T C 3_prime_UTR_variant LIRI-JP 16 3776721 3776721 single base substitution T C downstream_gene_variant LIRI-JP 16 3777966 3777966 single base substitution G A downstream_gene_variant LIRI-JP 16 3777966 3777966 single base substitution G A missense_variant S2323F 6968C>T LIRI-JP 16 3777966 3777966 single base substitution G A missense_variant S2361F 7082C>T LIRI-JP 16 3782411 3782411 deletion of <=200bp G - downstream_gene_variant LIRI-JP 16 3782411 3782411 deletion of <=200bp G - intron_variant LIRI-JP 16 3783263 3783263 single base substitution T C downstream_gene_variant LIRI-JP 16 3783263 3783263 single base substitution T C intron_variant LIRI-JP 16 3783923 3783923 single base substitution G A downstream_gene_variant LIRI-JP 16 3783923 3783923 single base substitution G A intron_variant LIRI-JP 16 3788186 3788186 single base substitution T C downstream_gene_variant LIRI-JP 16 3788186 3788186 single base substitution T C intron_variant LIRI-JP 16 3788186 3788186 single base substitution T C upstream_gene_variant LIRI-JP 16 3790910 3790910 single base substitution T C exon_variant LIRI-JP 16 3790910 3790910 single base substitution T C intron_variant LIRI-JP 16 3790910 3790910 single base substitution T C upstream_gene_variant LIRI-JP 16 3792660 3792660 single base substitution T C exon_variant LIRI-JP 16 3792660 3792660 single base substitution T C intron_variant LIRI-JP 16 3792789 3792789 single base substitution C G exon_variant LIRI-JP 16 3792789 3792789 single base substitution C G intron_variant LIRI-JP 16 3793298 3793298 single base substitution C A exon_variant LIRI-JP 16 3793298 3793298 single base substitution C A intron_variant LIRI-JP 16 3796175 3796175 single base substitution A C intron_variant LIRI-JP 16 3796175 3796175 single base substitution A C upstream_gene_variant LIRI-JP 16 3796418 3796418 single base substitution C T intron_variant LIRI-JP 16 3796418 3796418 single base substitution C T upstream_gene_variant LIRI-JP 16 3799259 3799259 single base substitution T G intron_variant LIRI-JP 16 3799259 3799259 single base substitution T G upstream_gene_variant LIRI-JP 16 3799317 3799317 single base substitution C T intron_variant LIRI-JP 16 3799317 3799317 single base substitution C T upstream_gene_variant LIRI-JP 16 3801520 3801520 single base substitution G A intron_variant LIRI-JP 16 3802045 3802045 single base substitution G C intron_variant LIRI-JP 16 3802045 3802045 single base substitution G C upstream_gene_variant LIRI-JP 16 3804080 3804080 single base substitution T C intron_variant LIRI-JP 16 3804080 3804080 single base substitution T C upstream_gene_variant LIRI-JP 16 3804866 3804866 single base substitution T C intron_variant LIRI-JP 16 3804866 3804866 single base substitution T C upstream_gene_variant LIRI-JP 16 3808224 3808224 single base substitution C T intron_variant LIRI-JP 16 3809233 3809233 deletion of <=200bp G - intron_variant LIRI-JP 16 3809877 3809877 single base substitution A C intron_variant LIRI-JP 16 3814073 3814073 single base substitution T C downstream_gene_variant LIRI-JP 16 3814073 3814073 single base substitution T C intron_variant LIRI-JP 16 3814248 3814248 single base substitution T C downstream_gene_variant LIRI-JP 16 3814248 3814248 single base substitution T C intron_variant LIRI-JP 16 3814510 3814510 single base substitution T C downstream_gene_variant LIRI-JP 16 3814510 3814510 single base substitution T C intron_variant LIRI-JP 16 3815151 3815151 single base substitution T C downstream_gene_variant LIRI-JP 16 3815151 3815151 single base substitution T C intron_variant LIRI-JP 16 3816878 3816878 single base substitution A C downstream_gene_variant LIRI-JP 16 3816878 3816878 single base substitution A C intron_variant LIRI-JP 16 3818626 3818626 single base substitution T C intron_variant LIRI-JP 16 3818626 3818626 single base substitution T C upstream_gene_variant LIRI-JP 16 3822790 3822790 single base substitution G A downstream_gene_variant LIRI-JP 16 3822790 3822790 single base substitution G A intron_variant LIRI-JP 16 3822790 3822790 single base substitution G A upstream_gene_variant LIRI-JP 16 3824137 3824137 single base substitution C T intron_variant LIRI-JP 16 3824137 3824137 single base substitution C T upstream_gene_variant LIRI-JP 16 3824247 3824247 single base substitution G A intron_variant LIRI-JP 16 3824247 3824247 single base substitution G A upstream_gene_variant LIRI-JP 16 3826805 3826805 single base substitution C T intron_variant LIRI-JP 16 3826805 3826805 single base substitution C T upstream_gene_variant LIRI-JP 16 3827592 3827592 single base substitution T C intron_variant LIRI-JP 16 3827592 3827592 single base substitution T C upstream_gene_variant LIRI-JP 16 3828699 3828699 single base substitution A G splice_donor_variant LIRI-JP 16 3828699 3828699 single base substitution A G upstream_gene_variant LIRI-JP 16 3829081 3829081 single base substitution T C intron_variant LIRI-JP 16 3829081 3829081 single base substitution T C upstream_gene_variant LIRI-JP 16 3830453 3830453 single base substitution G A intron_variant LIRI-JP 16 3830453 3830453 single base substitution G A upstream_gene_variant LIRI-JP 16 3830455 3830455 single base substitution T G intron_variant LIRI-JP 16 3830455 3830455 single base substitution T G upstream_gene_variant LIRI-JP 16 3830550 3830550 single base substitution C T intron_variant LIRI-JP 16 3830550 3830550 single base substitution C T upstream_gene_variant LIRI-JP 16 3832137 3832137 single base substitution C A intron_variant LIRI-JP 16 3832137 3832137 single base substitution C A upstream_gene_variant LIRI-JP 16 3832359 3832359 single base substitution A G intron_variant LIRI-JP 16 3832359 3832359 single base substitution A G upstream_gene_variant LIRI-JP 16 3835253 3835253 single base substitution T G intron_variant LIRI-JP 16 3835253 3835253 single base substitution T G upstream_gene_variant LIRI-JP 16 3835755 3835755 single base substitution C T intron_variant LIRI-JP 16 3835755 3835755 single base substitution C T upstream_gene_variant LIRI-JP 16 3835898 3835898 insertion of <=200bp - A intron_variant LIRI-JP 16 3842314 3842314 single base substitution T A intron_variant LIRI-JP 16 3843272 3843272 single base substitution A C intron_variant LIRI-JP 16 3846984 3846984 single base substitution T C intron_variant LIRI-JP 16 3850037 3850037 insertion of <=200bp - A intron_variant LIRI-JP 16 3852925 3852925 single base substitution G A intron_variant LIRI-JP 16 3853548 3853548 single base substitution A G intron_variant LIRI-JP 16 3856130 3856130 single base substitution C T intron_variant LIRI-JP 16 3859915 3859915 single base substitution C T intron_variant LIRI-JP 16 3860074 3860074 single base substitution T C intron_variant LIRI-JP 16 3860330 3860330 single base substitution G T intron_variant LIRI-JP 16 3861212 3861212 single base substitution C T intron_variant LIRI-JP 16 3861399 3861399 single base substitution C A intron_variant LIRI-JP 16 3863188 3863188 single base substitution T C intron_variant LIRI-JP 16 3863925 3863925 single base substitution T C intron_variant LIRI-JP 16 3864898 3864898 single base substitution C T intron_variant LIRI-JP 16 3867133 3867133 single base substitution C T intron_variant LIRI-JP 16 3870209 3870209 single base substitution A G intron_variant LIRI-JP 16 3870298 3870298 single base substitution T C intron_variant LIRI-JP 16 3871156 3871156 single base substitution G C intron_variant LIRI-JP 16 3871634 3871644 deletion of <=200bp TGCCCCTTTCA - intron_variant LIRI-JP 16 3872958 3872958 single base substitution T C intron_variant LIRI-JP 16 3874261 3874271 deletion of <=200bp GCTACGCCTCT - intron_variant LIRI-JP 16 3874695 3874695 single base substitution G A intron_variant LIRI-JP 16 3875684 3875684 single base substitution A C intron_variant LIRI-JP 16 3877926 3877926 single base substitution C A intron_variant LIRI-JP 16 3878494 3878494 single base substitution T C intron_variant LIRI-JP 16 3878750 3878750 single base substitution T C intron_variant LIRI-JP 16 3879532 3879532 single base substitution T C intron_variant LIRI-JP 16 3881455 3881455 single base substitution C T intron_variant LIRI-JP 16 3885152 3885152 single base substitution T C intron_variant LIRI-JP 16 3885382 3885382 single base substitution A T intron_variant LIRI-JP 16 3888013 3888013 single base substitution C T intron_variant LIRI-JP 16 3888685 3888685 single base substitution G C intron_variant LIRI-JP 16 3889328 3889328 single base substitution T C intron_variant LIRI-JP 16 3893350 3893350 single base substitution G A intron_variant LIRI-JP 16 3897136 3897136 single base substitution T G intron_variant LIRI-JP 16 3897724 3897724 single base substitution A G intron_variant LIRI-JP 16 3900520 3900520 single base substitution G C missense_variant N192K 576C>G LIRI-JP 16 3902636 3902636 single base substitution G T intron_variant LIRI-JP 16 3904151 3904160 deletion of <=200bp CCAGATAAGC - intron_variant LIRI-JP 16 3904682 3904682 single base substitution T C intron_variant LIRI-JP 16 3905359 3905359 single base substitution C T intron_variant LIRI-JP 16 3905555 3905555 single base substitution T C intron_variant LIRI-JP 16 3905932 3905932 single base substitution G A intron_variant LIRI-JP 16 3910238 3910238 single base substitution T C intron_variant LIRI-JP 16 3910301 3910301 single base substitution T C intron_variant LIRI-JP 16 3913029 3913029 single base substitution T C intron_variant LIRI-JP 16 3920023 3920023 single base substitution T C intron_variant LIRI-JP 16 3921542 3921542 single base substitution T C intron_variant LIRI-JP 16 3922120 3922120 single base substitution T C intron_variant LIRI-JP 16 3922353 3922353 single base substitution A G intron_variant LIRI-JP 16 3924068 3924068 single base substitution G C intron_variant LIRI-JP 16 3926131 3926131 single base substitution C T intron_variant LIRI-JP 16 3926313 3926313 single base substitution T G intron_variant LIRI-JP 16 3927793 3927793 single base substitution G A intron_variant LIRI-JP 16 3928139 3928139 single base substitution A T intron_variant LIRI-JP 16 3931721 3931721 single base substitution G A upstream_gene_variant LIRI-JP 16 3933197 3933197 single base substitution C T upstream_gene_variant LUSC-KR 16 3775352 3775352 single base substitution C G 3_prime_UTR_variant LUSC-KR 16 3775352 3775352 single base substitution C G downstream_gene_variant LUSC-KR 16 3775445 3775445 single base substitution G A 3_prime_UTR_variant LUSC-KR 16 3775445 3775445 single base substitution G A downstream_gene_variant LUSC-KR 16 3775962 3775962 single base substitution C T 3_prime_UTR_variant LUSC-KR 16 3775962 3775962 single base substitution C T downstream_gene_variant LUSC-KR 16 3776171 3776171 single base substitution T G 3_prime_UTR_variant LUSC-KR 16 3776171 3776171 single base substitution T G downstream_gene_variant LUSC-KR 16 3780869 3780869 single base substitution C A downstream_gene_variant LUSC-KR 16 3780869 3780869 single base substitution C A intron_variant LUSC-KR 16 3781106 3781106 single base substitution C G downstream_gene_variant LUSC-KR 16 3781106 3781106 single base substitution C G intron_variant LUSC-KR 16 3781308 3781308 single base substitution C T downstream_gene_variant LUSC-KR 16 3781308 3781308 single base substitution C T stop_gained W1648* 4943G>A LUSC-KR 16 3781308 3781308 single base substitution C T stop_gained W1686* 5057G>A LUSC-KR 16 3782734 3782734 single base substitution T C downstream_gene_variant LUSC-KR 16 3782734 3782734 single base substitution T C intron_variant LUSC-KR 16 3786951 3786951 single base substitution C A downstream_gene_variant LUSC-KR 16 3786951 3786951 single base substitution C A exon_variant LUSC-KR 16 3786951 3786951 single base substitution C A intron_variant LUSC-KR 16 3788618 3788618 single base substitution G A downstream_gene_variant LUSC-KR 16 3788618 3788618 single base substitution G A intron_variant LUSC-KR 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T LUSC-KR 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T LUSC-KR 16 3788618 3788618 single base substitution G A upstream_gene_variant LUSC-KR 16 3791717 3791717 single base substitution G C exon_variant LUSC-KR 16 3791717 3791717 single base substitution G C intron_variant LUSC-KR 16 3791717 3791717 single base substitution G C upstream_gene_variant LUSC-KR 16 3807892 3807892 single base substitution T A missense_variant K1138M 3413A>T LUSC-KR 16 3807892 3807892 single base substitution T A missense_variant K1176M 3527A>T LUSC-KR 16 3807892 3807892 single base substitution T A missense_variant K130M 389A>T LUSC-KR 16 3809623 3809623 single base substitution T C intron_variant LUSC-KR 16 3816803 3816803 single base substitution C T downstream_gene_variant LUSC-KR 16 3816803 3816803 single base substitution C T intron_variant LUSC-KR 16 3821820 3821820 single base substitution T A downstream_gene_variant LUSC-KR 16 3821820 3821820 single base substitution T A intron_variant LUSC-KR 16 3821820 3821820 single base substitution T A upstream_gene_variant LUSC-KR 16 3821821 3821821 single base substitution A T downstream_gene_variant LUSC-KR 16 3821821 3821821 single base substitution A T intron_variant LUSC-KR 16 3821821 3821821 single base substitution A T upstream_gene_variant LUSC-KR 16 3831187 3831187 single base substitution T A intron_variant LUSC-KR 16 3831187 3831187 single base substitution T A upstream_gene_variant LUSC-KR 16 3831230 3831230 single base substitution G T missense_variant L513I 1537C>A LUSC-KR 16 3831230 3831230 single base substitution G T missense_variant L551I 1651C>A LUSC-KR 16 3831230 3831230 single base substitution G T upstream_gene_variant LUSC-KR 16 3832959 3832959 single base substitution C A intron_variant LUSC-KR 16 3832959 3832959 single base substitution C A upstream_gene_variant LUSC-KR 16 3834525 3834525 single base substitution C A intron_variant LUSC-KR 16 3834525 3834525 single base substitution C A upstream_gene_variant LUSC-KR 16 3840695 3840695 single base substitution G A intron_variant LUSC-KR 16 3845855 3845855 single base substitution G A intron_variant LUSC-KR 16 3846074 3846074 single base substitution C G intron_variant LUSC-KR 16 3850786 3850786 single base substitution C T intron_variant LUSC-KR 16 3860640 3860640 single base substitution A G synonymous_variant D313D 939T>C LUSC-KR 16 3860839 3860839 single base substitution C T intron_variant LUSC-KR 16 3865551 3865551 single base substitution A T intron_variant LUSC-KR 16 3867151 3867151 single base substitution G C intron_variant LUSC-KR 16 3868168 3868168 single base substitution C T intron_variant LUSC-KR 16 3875137 3875137 single base substitution A G intron_variant LUSC-KR 16 3890792 3890792 single base substitution C A intron_variant LUSC-KR 16 3891114 3891114 single base substitution A C intron_variant LUSC-KR 16 3897216 3897216 single base substitution T C intron_variant LUSC-KR 16 3901213 3901213 single base substitution C A intron_variant LUSC-KR 16 3901861 3901861 single base substitution C A intron_variant LUSC-KR 16 3902059 3902059 single base substitution A C intron_variant LUSC-KR 16 3902064 3902064 single base substitution A C intron_variant LUSC-KR 16 3903861 3903861 single base substitution C A intron_variant LUSC-KR 16 3905455 3905455 single base substitution G A intron_variant LUSC-KR 16 3918508 3918508 single base substitution C A intron_variant LUSC-KR 16 3922700 3922700 single base substitution C A intron_variant LUSC-KR 16 3923930 3923930 single base substitution C A intron_variant LUSC-KR 16 3924420 3924420 single base substitution T A intron_variant LUSC-KR 16 3930892 3930892 single base substitution G A upstream_gene_variant LUSC-US 16 3777896 3777896 single base substitution G T downstream_gene_variant LUSC-US 16 3777896 3777896 single base substitution G T missense_variant H2346Q 7038C>A LUSC-US 16 3777896 3777896 single base substitution G T missense_variant H2384Q 7152C>A LUSC-US 16 3778059 3778059 single base substitution A C downstream_gene_variant LUSC-US 16 3778059 3778059 single base substitution A C missense_variant L2292R 6875T>G LUSC-US 16 3778059 3778059 single base substitution A C missense_variant L2330R 6989T>G LUSC-US 16 3778105 3778105 single base substitution T A downstream_gene_variant LUSC-US 16 3778105 3778105 single base substitution T A missense_variant S2277C 6829A>T LUSC-US 16 3778105 3778105 single base substitution T A missense_variant S2315C 6943A>T LUSC-US 16 3779748 3779748 single base substitution G A downstream_gene_variant LUSC-US 16 3779748 3779748 single base substitution G A missense_variant S1729L 5186C>T LUSC-US 16 3779748 3779748 single base substitution G A missense_variant S1767L 5300C>T LUSC-US 16 3788606 3788606 single base substitution A C downstream_gene_variant LUSC-US 16 3788606 3788606 single base substitution A C intron_variant LUSC-US 16 3788606 3788606 single base substitution A C missense_variant Y1412D 4234T>G LUSC-US 16 3788606 3788606 single base substitution A C missense_variant Y1450D 4348T>G LUSC-US 16 3788606 3788606 single base substitution A C upstream_gene_variant LUSC-US 16 3788618 3788618 single base substitution G A downstream_gene_variant LUSC-US 16 3788618 3788618 single base substitution G A intron_variant LUSC-US 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T LUSC-US 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T LUSC-US 16 3788618 3788618 single base substitution G A upstream_gene_variant LUSC-US 16 3788651 3788651 single base substitution C A downstream_gene_variant LUSC-US 16 3788651 3788651 single base substitution C A intron_variant LUSC-US 16 3788651 3788651 single base substitution C A missense_variant D1397Y 4189G>T LUSC-US 16 3788651 3788651 single base substitution C A missense_variant D1435Y 4303G>T LUSC-US 16 3788651 3788651 single base substitution C A upstream_gene_variant LUSC-US 16 3789636 3789636 single base substitution C T downstream_gene_variant LUSC-US 16 3789636 3789636 single base substitution C T exon_variant LUSC-US 16 3789636 3789636 single base substitution C T intron_variant LUSC-US 16 3789636 3789636 single base substitution C T missense_variant C1370Y 4109G>A LUSC-US 16 3789636 3789636 single base substitution C T missense_variant C1408Y 4223G>A LUSC-US 16 3789636 3789636 single base substitution C T missense_variant C176Y 527G>A LUSC-US 16 3789636 3789636 single base substitution C T missense_variant C281Y 842G>A LUSC-US 16 3789636 3789636 single base substitution C T upstream_gene_variant LUSC-US 16 3795299 3795299 single base substitution T C exon_variant LUSC-US 16 3795299 3795299 single base substitution T C missense_variant Y1260C 3779A>G LUSC-US 16 3795299 3795299 single base substitution T C missense_variant Y1298C 3893A>G LUSC-US 16 3795299 3795299 single base substitution T C missense_variant Y171C 512A>G LUSC-US 16 3795299 3795299 single base substitution T C missense_variant Y66C 197A>G LUSC-US 16 3795299 3795299 single base substitution T C upstream_gene_variant LUSC-US 16 3808000 3808000 single base substitution C T missense_variant R1102Q 3305G>A LUSC-US 16 3808000 3808000 single base substitution C T missense_variant R1140Q 3419G>A LUSC-US 16 3808000 3808000 single base substitution C T missense_variant R94Q 281G>A LUSC-US 16 3820624 3820624 single base substitution G A downstream_gene_variant LUSC-US 16 3820624 3820624 single base substitution G A exon_variant LUSC-US 16 3820624 3820624 single base substitution G A stop_gained Q905* 2713C>T LUSC-US 16 3820624 3820624 single base substitution G A stop_gained Q943* 2827C>T LUSC-US 16 3820624 3820624 single base substitution G A upstream_gene_variant LUSC-US 16 3823774 3823774 single base substitution G A exon_variant LUSC-US 16 3823774 3823774 single base substitution G A missense_variant P163L 488C>T LUSC-US 16 3823774 3823774 single base substitution G A missense_variant P236L 707C>T LUSC-US 16 3823774 3823774 single base substitution G A missense_variant P776L 2327C>T LUSC-US 16 3823774 3823774 single base substitution G A missense_variant P814L 2441C>T LUSC-US 16 3823774 3823774 single base substitution G A upstream_gene_variant LUSC-US 16 3823884 3823884 single base substitution A G exon_variant LUSC-US 16 3823884 3823884 single base substitution A G synonymous_variant G126G 378T>C LUSC-US 16 3823884 3823884 single base substitution A G synonymous_variant G199G 597T>C LUSC-US 16 3823884 3823884 single base substitution A G synonymous_variant G739G 2217T>C LUSC-US 16 3823884 3823884 single base substitution A G synonymous_variant G777G 2331T>C LUSC-US 16 3823884 3823884 single base substitution A G upstream_gene_variant LUSC-US 16 3828022 3828022 single base substitution C T synonymous_variant V138V 414G>A LUSC-US 16 3828022 3828022 single base substitution C T synonymous_variant V50V 150G>A LUSC-US 16 3828022 3828022 single base substitution C T synonymous_variant V663V 1989G>A LUSC-US 16 3828022 3828022 single base substitution C T synonymous_variant V701V 2103G>A LUSC-US 16 3828022 3828022 single base substitution C T upstream_gene_variant LUSC-US 16 3828795 3828795 single base substitution G C missense_variant P53R 158C>G LUSC-US 16 3828795 3828795 single base substitution G C missense_variant P578R 1733C>G LUSC-US 16 3828795 3828795 single base substitution G C missense_variant P616R 1847C>G LUSC-US 16 3828795 3828795 single base substitution G C upstream_gene_variant LUSC-US 16 3830746 3830746 single base substitution G A synonymous_variant L41L 121C>T LUSC-US 16 3830746 3830746 single base substitution G A synonymous_variant L566L 1696C>T LUSC-US 16 3830746 3830746 single base substitution G A synonymous_variant L604L 1810C>T LUSC-US 16 3830746 3830746 single base substitution G A upstream_gene_variant LUSC-US 16 3832751 3832751 single base substitution G A stop_gained Q465* 1393C>T LUSC-US 16 3832751 3832751 single base substitution G A stop_gained Q503* 1507C>T LUSC-US 16 3832751 3832751 single base substitution G A upstream_gene_variant LUSC-US 16 3832794 3832794 single base substitution G T synonymous_variant L450L 1350C>A LUSC-US 16 3832794 3832794 single base substitution G T synonymous_variant L488L 1464C>A LUSC-US 16 3832794 3832794 single base substitution G T upstream_gene_variant LUSC-US 16 3843455 3843455 single base substitution G C missense_variant P383R 1148C>G LUSC-US 16 3900414 3900414 single base substitution T C missense_variant T228A 682A>G LUSC-US 16 3900926 3900926 single base substitution C A missense_variant G57V 170G>T MALY-DE 16 3772299 3772299 single base substitution C T downstream_gene_variant MALY-DE 16 3774047 3774048 deletion of <=200bp TG - downstream_gene_variant MALY-DE 16 3781324 3781326 deletion of <=200bp AGG - disruptive_inframe_deletion SL1642L MALY-DE 16 3781324 3781326 deletion of <=200bp AGG - disruptive_inframe_deletion SL1680L MALY-DE 16 3781324 3781326 deletion of <=200bp AGG - downstream_gene_variant MALY-DE 16 3781421 3781421 deletion of <=200bp G - downstream_gene_variant MALY-DE 16 3781421 3781421 deletion of <=200bp G - frameshift_variant P1610 MALY-DE 16 3781421 3781421 deletion of <=200bp G - frameshift_variant P1648 MALY-DE 16 3781421 3781421 insertion of <=200bp - G downstream_gene_variant MALY-DE 16 3781421 3781421 insertion of <=200bp - G frameshift_variant P1610P? MALY-DE 16 3781421 3781421 insertion of <=200bp - G frameshift_variant P1648P? MALY-DE 16 3786703 3786703 single base substitution T A downstream_gene_variant MALY-DE 16 3786703 3786703 single base substitution T A exon_variant MALY-DE 16 3786703 3786703 single base substitution T A missense_variant Y1465F 4394A>T MALY-DE 16 3786703 3786703 single base substitution T A missense_variant Y1503F 4508A>T MALY-DE 16 3786703 3786703 single base substitution T G downstream_gene_variant MALY-DE 16 3786703 3786703 single base substitution T G exon_variant MALY-DE 16 3786703 3786703 single base substitution T G missense_variant Y1465S 4394A>C MALY-DE 16 3786703 3786703 single base substitution T G missense_variant Y1503S 4508A>C MALY-DE 16 3786704 3786704 single base substitution A C downstream_gene_variant MALY-DE 16 3786704 3786704 single base substitution A C exon_variant MALY-DE 16 3786704 3786704 single base substitution A C missense_variant Y1465D 4393T>G MALY-DE 16 3786704 3786704 single base substitution A C missense_variant Y1503D 4507T>G MALY-DE 16 3786704 3786704 single base substitution A G downstream_gene_variant MALY-DE 16 3786704 3786704 single base substitution A G exon_variant MALY-DE 16 3786704 3786704 single base substitution A G missense_variant Y1465H 4393T>C MALY-DE 16 3786704 3786704 single base substitution A G missense_variant Y1503H 4507T>C MALY-DE 16 3786707 3786707 single base substitution A G downstream_gene_variant MALY-DE 16 3786707 3786707 single base substitution A G exon_variant MALY-DE 16 3786707 3786707 single base substitution A G missense_variant W1464R 4390T>C MALY-DE 16 3786707 3786707 single base substitution A G missense_variant W1502R 4504T>C MALY-DE 16 3786715 3786715 single base substitution A G downstream_gene_variant MALY-DE 16 3786715 3786715 single base substitution A G exon_variant MALY-DE 16 3786715 3786715 single base substitution A G missense_variant L1461P 4382T>C MALY-DE 16 3786715 3786715 single base substitution A G missense_variant L1499P 4496T>C MALY-DE 16 3786715 3786715 single base substitution A T downstream_gene_variant MALY-DE 16 3786715 3786715 single base substitution A T exon_variant MALY-DE 16 3786715 3786715 single base substitution A T missense_variant L1461Q 4382T>A MALY-DE 16 3786715 3786715 single base substitution A T missense_variant L1499Q 4496T>A MALY-DE 16 3786740 3786740 single base substitution G C downstream_gene_variant MALY-DE 16 3786740 3786740 single base substitution G C exon_variant MALY-DE 16 3786740 3786740 single base substitution G C missense_variant Q1453E 4357C>G MALY-DE 16 3786740 3786740 single base substitution G C missense_variant Q1491E 4471C>G MALY-DE 16 3786748 3786748 single base substitution G A downstream_gene_variant MALY-DE 16 3786748 3786748 single base substitution G A exon_variant MALY-DE 16 3786748 3786748 single base substitution G A missense_variant P1450L 4349C>T MALY-DE 16 3786748 3786748 single base substitution G A missense_variant P1488L 4463C>T MALY-DE 16 3786763 3786763 single base substitution A G downstream_gene_variant MALY-DE 16 3786763 3786763 single base substitution A G exon_variant MALY-DE 16 3786763 3786763 single base substitution A G missense_variant I1445T 4334T>C MALY-DE 16 3786763 3786763 single base substitution A G missense_variant I1483T 4448T>C MALY-DE 16 3786767 3786767 single base substitution A G downstream_gene_variant MALY-DE 16 3786767 3786767 single base substitution A G exon_variant MALY-DE 16 3786767 3786767 single base substitution A G missense_variant Y1444H 4330T>C MALY-DE 16 3786767 3786767 single base substitution A G missense_variant Y1482H 4444T>C MALY-DE 16 3788563 3788563 single base substitution A T downstream_gene_variant MALY-DE 16 3788563 3788563 single base substitution A T intron_variant MALY-DE 16 3788563 3788563 single base substitution A T stop_gained L1426* 4277T>A MALY-DE 16 3788563 3788563 single base substitution A T stop_gained L1464* 4391T>A MALY-DE 16 3788563 3788563 single base substitution A T upstream_gene_variant MALY-DE 16 3788618 3788618 single base substitution G A downstream_gene_variant MALY-DE 16 3788618 3788618 single base substitution G A intron_variant MALY-DE 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T MALY-DE 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T MALY-DE 16 3788618 3788618 single base substitution G A upstream_gene_variant MALY-DE 16 3788646 3788646 single base substitution A T downstream_gene_variant MALY-DE 16 3788646 3788646 single base substitution A T intron_variant MALY-DE 16 3788646 3788646 single base substitution A T missense_variant S1398R 4194T>A MALY-DE 16 3788646 3788646 single base substitution A T missense_variant S1436R 4308T>A MALY-DE 16 3788646 3788646 single base substitution A T upstream_gene_variant MALY-DE 16 3788653 3788653 single base substitution A T downstream_gene_variant MALY-DE 16 3788653 3788653 single base substitution A T intron_variant MALY-DE 16 3788653 3788653 single base substitution A T missense_variant L1396Q 4187T>A MALY-DE 16 3788653 3788653 single base substitution A T missense_variant L1434Q 4301T>A MALY-DE 16 3788653 3788653 single base substitution A T upstream_gene_variant MALY-DE 16 3788661 3788661 single base substitution A G downstream_gene_variant MALY-DE 16 3788661 3788661 single base substitution A G intron_variant MALY-DE 16 3788661 3788661 single base substitution A G synonymous_variant I1393I 4179T>C MALY-DE 16 3788661 3788661 single base substitution A G synonymous_variant I1431I 4293T>C MALY-DE 16 3788661 3788661 single base substitution A G upstream_gene_variant MALY-DE 16 3788662 3788662 single base substitution A G downstream_gene_variant MALY-DE 16 3788662 3788662 single base substitution A G intron_variant MALY-DE 16 3788662 3788662 single base substitution A G missense_variant I1393T 4178T>C MALY-DE 16 3788662 3788662 single base substitution A G missense_variant I1431T 4292T>C MALY-DE 16 3788662 3788662 single base substitution A G upstream_gene_variant MALY-DE 16 3788724 3788724 single base substitution T C downstream_gene_variant MALY-DE 16 3788724 3788724 single base substitution T C intron_variant MALY-DE 16 3788724 3788724 single base substitution T C upstream_gene_variant MALY-DE 16 3789616 3789616 single base substitution G A downstream_gene_variant MALY-DE 16 3789616 3789616 single base substitution G A exon_variant MALY-DE 16 3789616 3789616 single base substitution G A intron_variant MALY-DE 16 3789616 3789616 single base substitution G A stop_gained Q1377* 4129C>T MALY-DE 16 3789616 3789616 single base substitution G A stop_gained Q1415* 4243C>T MALY-DE 16 3789616 3789616 single base substitution G A stop_gained Q183* 547C>T MALY-DE 16 3789616 3789616 single base substitution G A synonymous_variant ?288 MALY-DE 16 3789616 3789616 single base substitution G A upstream_gene_variant MALY-DE 16 3790545 3790545 single base substitution G A exon_variant MALY-DE 16 3790545 3790545 single base substitution G A stop_gained Q1292* 3874C>T MALY-DE 16 3790545 3790545 single base substitution G A stop_gained Q1330* 3988C>T MALY-DE 16 3790545 3790545 single base substitution G A stop_gained Q203* 607C>T MALY-DE 16 3790545 3790545 single base substitution G A stop_gained Q98* 292C>T MALY-DE 16 3790545 3790545 single base substitution G A upstream_gene_variant MALY-DE 16 3792038 3792038 single base substitution C T exon_variant MALY-DE 16 3792038 3792038 single base substitution C T intron_variant MALY-DE 16 3799627 3799627 single base substitution C T splice_donor_variant MALY-DE 16 3799627 3799627 single base substitution C T upstream_gene_variant MALY-DE 16 3802414 3802414 single base substitution A C intron_variant MALY-DE 16 3802414 3802414 single base substitution A C upstream_gene_variant MALY-DE 16 3802516 3802516 single base substitution A T intron_variant MALY-DE 16 3802516 3802516 single base substitution A T upstream_gene_variant MALY-DE 16 3806529 3806529 single base substitution C A intron_variant MALY-DE 16 3806529 3806529 single base substitution C A upstream_gene_variant MALY-DE 16 3807810 3807810 single base substitution C T intron_variant MALY-DE 16 3807810 3807810 single base substitution C T splice_region_variant MALY-DE 16 3808044 3808044 single base substitution A T stop_gained Y1087* 3261T>A MALY-DE 16 3808044 3808044 single base substitution A T stop_gained Y1125* 3375T>A MALY-DE 16 3808044 3808044 single base substitution A T stop_gained Y79* 237T>A MALY-DE 16 3808181 3808181 single base substitution A G intron_variant MALY-DE 16 3809104 3809104 single base substitution C T intron_variant MALY-DE 16 3810675 3810675 single base substitution G A intron_variant MALY-DE 16 3813483 3813483 single base substitution C T downstream_gene_variant MALY-DE 16 3813483 3813483 single base substitution C T intron_variant MALY-DE 16 3815388 3815388 deletion of <=200bp G - downstream_gene_variant MALY-DE 16 3815388 3815388 deletion of <=200bp G - intron_variant MALY-DE 16 3815545 3815545 insertion of <=200bp - GACAACT downstream_gene_variant MALY-DE 16 3815545 3815545 insertion of <=200bp - GACAACT intron_variant MALY-DE 16 3815816 3815817 deletion of <=200bp TT - downstream_gene_variant MALY-DE 16 3815816 3815817 deletion of <=200bp TT - intron_variant MALY-DE 16 3817719 3817719 single base substitution A C exon_variant MALY-DE 16 3817719 3817719 single base substitution A C splice_donor_variant MALY-DE 16 3818463 3818463 single base substitution T A intron_variant MALY-DE 16 3818463 3818463 single base substitution T A upstream_gene_variant MALY-DE 16 3823811 3823811 insertion of <=200bp - A exon_variant MALY-DE 16 3823811 3823811 insertion of <=200bp - A frameshift_variant S151F? MALY-DE 16 3823811 3823811 insertion of <=200bp - A frameshift_variant S224F? MALY-DE 16 3823811 3823811 insertion of <=200bp - A frameshift_variant S764F? MALY-DE 16 3823811 3823811 insertion of <=200bp - A frameshift_variant S802F? MALY-DE 16 3823811 3823811 insertion of <=200bp - A upstream_gene_variant MALY-DE 16 3823847 3823847 single base substitution G A exon_variant MALY-DE 16 3823847 3823847 single base substitution G A stop_gained Q139* 415C>T MALY-DE 16 3823847 3823847 single base substitution G A stop_gained Q212* 634C>T MALY-DE 16 3823847 3823847 single base substitution G A stop_gained Q752* 2254C>T MALY-DE 16 3823847 3823847 single base substitution G A stop_gained Q790* 2368C>T MALY-DE 16 3823847 3823847 single base substitution G A upstream_gene_variant MALY-DE 16 3824733 3824733 single base substitution C T exon_variant MALY-DE 16 3824733 3824733 single base substitution C T intron_variant MALY-DE 16 3824733 3824733 single base substitution C T upstream_gene_variant MALY-DE 16 3824823 3824823 single base substitution C A intron_variant MALY-DE 16 3824823 3824823 single base substitution C A upstream_gene_variant MALY-DE 16 3826553 3826553 single base substitution C A intron_variant MALY-DE 16 3826553 3826553 single base substitution C A upstream_gene_variant MALY-DE 16 3827367 3827370 deletion of <=200bp AAAT - intron_variant MALY-DE 16 3827367 3827370 deletion of <=200bp AAAT - upstream_gene_variant MALY-DE 16 3828014 3828014 deletion of <=200bp G - frameshift_variant P141 MALY-DE 16 3828014 3828014 deletion of <=200bp G - frameshift_variant P53 MALY-DE 16 3828014 3828014 deletion of <=200bp G - frameshift_variant P666 MALY-DE 16 3828014 3828014 deletion of <=200bp G - frameshift_variant P704 MALY-DE 16 3828014 3828014 deletion of <=200bp G - upstream_gene_variant MALY-DE 16 3828073 3828076 deletion of <=200bp GGCT - frameshift_variant PA120 MALY-DE 16 3828073 3828076 deletion of <=200bp GGCT - frameshift_variant PA32 MALY-DE 16 3828073 3828076 deletion of <=200bp GGCT - frameshift_variant PA645 MALY-DE 16 3828073 3828076 deletion of <=200bp GGCT - frameshift_variant PA683 MALY-DE 16 3828073 3828076 deletion of <=200bp GGCT - upstream_gene_variant MALY-DE 16 3829610 3829610 single base substitution G C intron_variant MALY-DE 16 3829610 3829610 single base substitution G C upstream_gene_variant MALY-DE 16 3830764 3830764 single base substitution G A stop_gained Q35* 103C>T MALY-DE 16 3830764 3830764 single base substitution G A stop_gained Q560* 1678C>T MALY-DE 16 3830764 3830764 single base substitution G A stop_gained Q598* 1792C>T MALY-DE 16 3830764 3830764 single base substitution G A upstream_gene_variant MALY-DE 16 3830781 3830781 single base substitution C T stop_gained W29* 86G>A MALY-DE 16 3830781 3830781 single base substitution C T stop_gained W554* 1661G>A MALY-DE 16 3830781 3830781 single base substitution C T stop_gained W592* 1775G>A MALY-DE 16 3830781 3830781 single base substitution C T upstream_gene_variant MALY-DE 16 3833490 3833490 single base substitution A G intron_variant MALY-DE 16 3833490 3833490 single base substitution A G upstream_gene_variant MALY-DE 16 3837611 3837611 single base substitution C G intron_variant MALY-DE 16 3838701 3838701 single base substitution C T intron_variant MALY-DE 16 3854048 3854048 single base substitution G A intron_variant MALY-DE 16 3860723 3860723 single base substitution G A stop_gained Q286* 856C>T MALY-DE 16 3870445 3870445 single base substitution G T intron_variant MALY-DE 16 3880784 3880784 single base substitution T G intron_variant MALY-DE 16 3881014 3881014 single base substitution C A intron_variant MALY-DE 16 3881558 3881558 single base substitution C T intron_variant MALY-DE 16 3888587 3888587 single base substitution T C intron_variant MALY-DE 16 3895006 3895006 single base substitution A G intron_variant MALY-DE 16 3897666 3897666 single base substitution G A intron_variant MALY-DE 16 3897828 3897828 single base substitution G C intron_variant MALY-DE 16 3900499 3900502 deletion of <=200bp ATTA - frameshift_variant IN198 MALY-DE 16 3904512 3904512 single base substitution T C intron_variant MALY-DE 16 3906494 3906494 single base substitution T A intron_variant MALY-DE 16 3910868 3910868 single base substitution G C intron_variant MALY-DE 16 3916663 3916663 insertion of <=200bp - A intron_variant MALY-DE 16 3924933 3924933 single base substitution G A intron_variant MALY-DE 16 3925058 3925058 single base substitution C T intron_variant MALY-DE 16 3926331 3926331 single base substitution A G intron_variant MALY-DE 16 3935050 3935050 single base substitution C T upstream_gene_variant MELA-AU 16 3770854 3770854 single base substitution G T downstream_gene_variant MELA-AU 16 3771001 3771001 single base substitution G A downstream_gene_variant MELA-AU 16 3771218 3771218 single base substitution G A downstream_gene_variant MELA-AU 16 3771260 3771260 single base substitution G A downstream_gene_variant MELA-AU 16 3771635 3771635 single base substitution G A downstream_gene_variant MELA-AU 16 3771676 3771676 single base substitution G A downstream_gene_variant MELA-AU 16 3771725 3771725 single base substitution C T downstream_gene_variant MELA-AU 16 3771783 3771783 single base substitution G A downstream_gene_variant MELA-AU 16 3771789 3771789 single base substitution G A downstream_gene_variant MELA-AU 16 3771804 3771804 single base substitution G A downstream_gene_variant MELA-AU 16 3771808 3771808 single base substitution G A downstream_gene_variant MELA-AU 16 3772290 3772290 single base substitution G A downstream_gene_variant MELA-AU 16 3772622 3772622 single base substitution A G downstream_gene_variant MELA-AU 16 3772678 3772678 single base substitution G A downstream_gene_variant MELA-AU 16 3773102 3773102 single base substitution G A downstream_gene_variant MELA-AU 16 3773584 3773584 single base substitution G A downstream_gene_variant MELA-AU 16 3773610 3773610 single base substitution G A downstream_gene_variant MELA-AU 16 3774364 3774364 single base substitution C T downstream_gene_variant MELA-AU 16 3774904 3774905 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 3774984 3774984 single base substitution G A downstream_gene_variant MELA-AU 16 3775180 3775180 deletion of <=200bp G - 3_prime_UTR_variant MELA-AU 16 3775180 3775180 deletion of <=200bp G - downstream_gene_variant MELA-AU 16 3775329 3775329 single base substitution T C 3_prime_UTR_variant MELA-AU 16 3775329 3775329 single base substitution T C downstream_gene_variant MELA-AU 16 3775595 3775595 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3775595 3775595 single base substitution G A downstream_gene_variant MELA-AU 16 3775813 3775813 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3775813 3775813 single base substitution G A downstream_gene_variant MELA-AU 16 3776352 3776352 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3776352 3776352 single base substitution G A downstream_gene_variant MELA-AU 16 3776522 3776522 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3776522 3776522 single base substitution G A downstream_gene_variant MELA-AU 16 3778280 3778280 single base substitution G A downstream_gene_variant MELA-AU 16 3778280 3778280 single base substitution G A synonymous_variant L2218L 6654C>T MELA-AU 16 3778280 3778280 single base substitution G A synonymous_variant L2256L 6768C>T MELA-AU 16 3778285 3778285 single base substitution G A downstream_gene_variant MELA-AU 16 3778285 3778285 single base substitution G A missense_variant P2217S 6649C>T MELA-AU 16 3778285 3778285 single base substitution G A missense_variant P2255S 6763C>T MELA-AU 16 3779649 3779649 single base substitution C T downstream_gene_variant MELA-AU 16 3779649 3779649 single base substitution C T missense_variant R1762Q 5285G>A MELA-AU 16 3779649 3779649 single base substitution C T missense_variant R1800Q 5399G>A MELA-AU 16 3779715 3779715 single base substitution G C downstream_gene_variant MELA-AU 16 3779715 3779715 single base substitution G C missense_variant S1740W 5219C>G MELA-AU 16 3779715 3779715 single base substitution G C missense_variant S1778W 5333C>G MELA-AU 16 3780054 3780054 single base substitution G A downstream_gene_variant MELA-AU 16 3780054 3780054 single base substitution G A intron_variant MELA-AU 16 3780620 3780620 single base substitution G A downstream_gene_variant MELA-AU 16 3780620 3780620 single base substitution G A intron_variant MELA-AU 16 3780729 3780729 single base substitution T C downstream_gene_variant MELA-AU 16 3780729 3780729 single base substitution T C intron_variant MELA-AU 16 3781023 3781023 single base substitution G A downstream_gene_variant MELA-AU 16 3781023 3781023 single base substitution G A intron_variant MELA-AU 16 3781653 3781653 single base substitution C T downstream_gene_variant MELA-AU 16 3781653 3781653 single base substitution C T intron_variant MELA-AU 16 3782431 3782431 single base substitution G A downstream_gene_variant MELA-AU 16 3782431 3782431 single base substitution G A intron_variant MELA-AU 16 3783451 3783451 single base substitution G A downstream_gene_variant MELA-AU 16 3783451 3783451 single base substitution G A intron_variant MELA-AU 16 3783466 3783466 single base substitution G A downstream_gene_variant MELA-AU 16 3783466 3783466 single base substitution G A intron_variant MELA-AU 16 3783692 3783692 single base substitution G A downstream_gene_variant MELA-AU 16 3783692 3783692 single base substitution G A intron_variant MELA-AU 16 3784507 3784507 single base substitution G A downstream_gene_variant MELA-AU 16 3784507 3784507 single base substitution G A intron_variant MELA-AU 16 3784508 3784508 single base substitution G A downstream_gene_variant MELA-AU 16 3784508 3784508 single base substitution G A intron_variant MELA-AU 16 3785187 3785187 single base substitution A G downstream_gene_variant MELA-AU 16 3785187 3785187 single base substitution A G intron_variant MELA-AU 16 3785345 3785345 single base substitution T C downstream_gene_variant MELA-AU 16 3785345 3785345 single base substitution T C intron_variant MELA-AU 16 3785432 3785432 single base substitution G A downstream_gene_variant MELA-AU 16 3785432 3785432 single base substitution G A intron_variant MELA-AU 16 3785598 3785598 single base substitution G A downstream_gene_variant MELA-AU 16 3785598 3785598 single base substitution G A intron_variant MELA-AU 16 3785840 3785840 single base substitution G A downstream_gene_variant MELA-AU 16 3785840 3785840 single base substitution G A intron_variant MELA-AU 16 3786798 3786798 single base substitution G C downstream_gene_variant MELA-AU 16 3786798 3786798 single base substitution G C exon_variant MELA-AU 16 3786798 3786798 single base substitution G C missense_variant I1433M 4299C>G MELA-AU 16 3786798 3786798 single base substitution G C missense_variant I1471M 4413C>G MELA-AU 16 3786857 3786857 single base substitution G A downstream_gene_variant MELA-AU 16 3786857 3786857 single base substitution G A exon_variant MELA-AU 16 3786857 3786857 single base substitution G A intron_variant MELA-AU 16 3786864 3786864 single base substitution G A downstream_gene_variant MELA-AU 16 3786864 3786864 single base substitution G A exon_variant MELA-AU 16 3786864 3786864 single base substitution G A intron_variant MELA-AU 16 3787089 3787089 single base substitution G A downstream_gene_variant MELA-AU 16 3787089 3787089 single base substitution G A intron_variant MELA-AU 16 3787089 3787089 single base substitution G A upstream_gene_variant MELA-AU 16 3787151 3787151 single base substitution G A downstream_gene_variant MELA-AU 16 3787151 3787151 single base substitution G A intron_variant MELA-AU 16 3787151 3787151 single base substitution G A upstream_gene_variant MELA-AU 16 3787353 3787356 deletion of <=200bp GATT - downstream_gene_variant MELA-AU 16 3787353 3787356 deletion of <=200bp GATT - intron_variant MELA-AU 16 3787353 3787356 deletion of <=200bp GATT - upstream_gene_variant MELA-AU 16 3787428 3787428 single base substitution G A downstream_gene_variant MELA-AU 16 3787428 3787428 single base substitution G A intron_variant MELA-AU 16 3787428 3787428 single base substitution G A upstream_gene_variant MELA-AU 16 3787476 3787477 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 3787476 3787477 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3787476 3787477 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 3788273 3788273 single base substitution A C downstream_gene_variant MELA-AU 16 3788273 3788273 single base substitution A C intron_variant MELA-AU 16 3788273 3788273 single base substitution A C upstream_gene_variant MELA-AU 16 3788278 3788278 single base substitution G A downstream_gene_variant MELA-AU 16 3788278 3788278 single base substitution G A intron_variant MELA-AU 16 3788278 3788278 single base substitution G A upstream_gene_variant MELA-AU 16 3788380 3788380 single base substitution G A downstream_gene_variant MELA-AU 16 3788380 3788380 single base substitution G A intron_variant MELA-AU 16 3788380 3788380 single base substitution G A upstream_gene_variant MELA-AU 16 3788497 3788497 single base substitution A G downstream_gene_variant MELA-AU 16 3788497 3788497 single base substitution A G intron_variant MELA-AU 16 3788497 3788497 single base substitution A G upstream_gene_variant MELA-AU 16 3788841 3788841 single base substitution G A downstream_gene_variant MELA-AU 16 3788841 3788841 single base substitution G A intron_variant MELA-AU 16 3788841 3788841 single base substitution G A upstream_gene_variant MELA-AU 16 3789319 3789319 single base substitution C A downstream_gene_variant MELA-AU 16 3789319 3789319 single base substitution C A intron_variant MELA-AU 16 3789319 3789319 single base substitution C A upstream_gene_variant MELA-AU 16 3789343 3789343 single base substitution A T downstream_gene_variant MELA-AU 16 3789343 3789343 single base substitution A T intron_variant MELA-AU 16 3789343 3789343 single base substitution A T upstream_gene_variant MELA-AU 16 3791385 3791385 single base substitution G A exon_variant MELA-AU 16 3791385 3791385 single base substitution G A intron_variant MELA-AU 16 3791385 3791385 single base substitution G A upstream_gene_variant MELA-AU 16 3791630 3791630 single base substitution A G exon_variant MELA-AU 16 3791630 3791630 single base substitution A G intron_variant MELA-AU 16 3791630 3791630 single base substitution A G upstream_gene_variant MELA-AU 16 3791727 3791728 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 16 3791727 3791728 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3791727 3791728 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 3791759 3791759 single base substitution G A exon_variant MELA-AU 16 3791759 3791759 single base substitution G A intron_variant MELA-AU 16 3791759 3791759 single base substitution G A upstream_gene_variant MELA-AU 16 3791814 3791814 single base substitution T A exon_variant MELA-AU 16 3791814 3791814 single base substitution T A intron_variant MELA-AU 16 3791814 3791814 single base substitution T A upstream_gene_variant MELA-AU 16 3791826 3791826 single base substitution C T exon_variant MELA-AU 16 3791826 3791826 single base substitution C T intron_variant MELA-AU 16 3791826 3791826 single base substitution C T upstream_gene_variant MELA-AU 16 3791859 3791859 single base substitution G A exon_variant MELA-AU 16 3791859 3791859 single base substitution G A intron_variant MELA-AU 16 3791859 3791859 single base substitution G A upstream_gene_variant MELA-AU 16 3792113 3792113 single base substitution A G exon_variant MELA-AU 16 3792113 3792113 single base substitution A G intron_variant MELA-AU 16 3792414 3792414 single base substitution G A exon_variant MELA-AU 16 3792414 3792414 single base substitution G A intron_variant MELA-AU 16 3793255 3793255 single base substitution G A exon_variant MELA-AU 16 3793255 3793255 single base substitution G A intron_variant MELA-AU 16 3793294 3793294 single base substitution G A exon_variant MELA-AU 16 3793294 3793294 single base substitution G A intron_variant MELA-AU 16 3793718 3793718 single base substitution G A intron_variant MELA-AU 16 3793718 3793718 single base substitution G A upstream_gene_variant MELA-AU 16 3793791 3793791 single base substitution A C intron_variant MELA-AU 16 3793791 3793791 single base substitution A C upstream_gene_variant MELA-AU 16 3793802 3793802 deletion of <=200bp G - intron_variant MELA-AU 16 3793802 3793802 deletion of <=200bp G - upstream_gene_variant MELA-AU 16 3793806 3793806 single base substitution G T intron_variant MELA-AU 16 3793806 3793806 single base substitution G T upstream_gene_variant MELA-AU 16 3793842 3793842 single base substitution G A intron_variant MELA-AU 16 3793842 3793842 single base substitution G A upstream_gene_variant MELA-AU 16 3794321 3794321 single base substitution G A intron_variant MELA-AU 16 3794321 3794321 single base substitution G A upstream_gene_variant MELA-AU 16 3794773 3794773 single base substitution G A intron_variant MELA-AU 16 3794773 3794773 single base substitution G A upstream_gene_variant MELA-AU 16 3794831 3794831 single base substitution G A intron_variant MELA-AU 16 3794831 3794831 single base substitution G A upstream_gene_variant MELA-AU 16 3795532 3795532 single base substitution C T exon_variant MELA-AU 16 3795532 3795532 single base substitution C T intron_variant MELA-AU 16 3795532 3795532 single base substitution C T upstream_gene_variant MELA-AU 16 3795590 3795590 insertion of <=200bp - AAT exon_variant MELA-AU 16 3795590 3795590 insertion of <=200bp - AAT intron_variant MELA-AU 16 3795590 3795590 insertion of <=200bp - AAT upstream_gene_variant MELA-AU 16 3795764 3795764 single base substitution C T intron_variant MELA-AU 16 3795764 3795764 single base substitution C T upstream_gene_variant MELA-AU 16 3796158 3796158 single base substitution G A intron_variant MELA-AU 16 3796158 3796158 single base substitution G A upstream_gene_variant MELA-AU 16 3796527 3796527 single base substitution G A intron_variant MELA-AU 16 3796527 3796527 single base substitution G A upstream_gene_variant MELA-AU 16 3796636 3796636 single base substitution G A intron_variant MELA-AU 16 3796636 3796636 single base substitution G A upstream_gene_variant MELA-AU 16 3796637 3796637 single base substitution G A intron_variant MELA-AU 16 3796637 3796637 single base substitution G A upstream_gene_variant MELA-AU 16 3796871 3796871 single base substitution G C intron_variant MELA-AU 16 3796871 3796871 single base substitution G C upstream_gene_variant MELA-AU 16 3797746 3797746 single base substitution G A intron_variant MELA-AU 16 3797746 3797746 single base substitution G A upstream_gene_variant MELA-AU 16 3797823 3797823 single base substitution G A intron_variant MELA-AU 16 3797823 3797823 single base substitution G A upstream_gene_variant MELA-AU 16 3798067 3798067 single base substitution G A intron_variant MELA-AU 16 3798067 3798067 single base substitution G A upstream_gene_variant MELA-AU 16 3798528 3798528 single base substitution C T intron_variant MELA-AU 16 3798528 3798528 single base substitution C T upstream_gene_variant MELA-AU 16 3798595 3798595 single base substitution G A intron_variant MELA-AU 16 3798595 3798595 single base substitution G A upstream_gene_variant MELA-AU 16 3798669 3798669 single base substitution G A intron_variant MELA-AU 16 3798669 3798669 single base substitution G A upstream_gene_variant MELA-AU 16 3798835 3798835 single base substitution C T intron_variant MELA-AU 16 3798835 3798835 single base substitution C T upstream_gene_variant MELA-AU 16 3799510 3799510 single base substitution A C intron_variant MELA-AU 16 3799510 3799510 single base substitution A C upstream_gene_variant MELA-AU 16 3800164 3800164 single base substitution G T intron_variant MELA-AU 16 3800164 3800164 single base substitution G T upstream_gene_variant MELA-AU 16 3800166 3800166 single base substitution T C intron_variant MELA-AU 16 3800166 3800166 single base substitution T C upstream_gene_variant MELA-AU 16 3801421 3801421 single base substitution T C intron_variant MELA-AU 16 3801667 3801667 single base substitution G A intron_variant MELA-AU 16 3802784 3802784 single base substitution A C intron_variant MELA-AU 16 3802784 3802784 single base substitution A C upstream_gene_variant MELA-AU 16 3803101 3803101 single base substitution G A intron_variant MELA-AU 16 3803101 3803101 single base substitution G A upstream_gene_variant MELA-AU 16 3803118 3803118 single base substitution G A intron_variant MELA-AU 16 3803118 3803118 single base substitution G A upstream_gene_variant MELA-AU 16 3803173 3803173 single base substitution A C intron_variant MELA-AU 16 3803173 3803173 single base substitution A C upstream_gene_variant MELA-AU 16 3803646 3803646 single base substitution C T intron_variant MELA-AU 16 3803646 3803646 single base substitution C T upstream_gene_variant MELA-AU 16 3803887 3803887 deletion of <=200bp A - intron_variant MELA-AU 16 3803887 3803887 deletion of <=200bp A - upstream_gene_variant MELA-AU 16 3804109 3804109 single base substitution G A intron_variant MELA-AU 16 3804109 3804109 single base substitution G A upstream_gene_variant MELA-AU 16 3804529 3804529 single base substitution C T intron_variant MELA-AU 16 3804529 3804529 single base substitution C T upstream_gene_variant MELA-AU 16 3804568 3804568 single base substitution G C intron_variant MELA-AU 16 3804568 3804568 single base substitution G C upstream_gene_variant MELA-AU 16 3805305 3805305 single base substitution G A intron_variant MELA-AU 16 3805305 3805305 single base substitution G A upstream_gene_variant MELA-AU 16 3805587 3805587 single base substitution T C intron_variant MELA-AU 16 3805587 3805587 single base substitution T C upstream_gene_variant MELA-AU 16 3807176 3807176 single base substitution G A intron_variant MELA-AU 16 3808291 3808291 single base substitution G A intron_variant MELA-AU 16 3809491 3809491 single base substitution G A intron_variant MELA-AU 16 3809697 3809697 single base substitution A G intron_variant MELA-AU 16 3811230 3811230 single base substitution G A intron_variant MELA-AU 16 3812256 3812256 single base substitution G A intron_variant MELA-AU 16 3812317 3812317 single base substitution T A downstream_gene_variant MELA-AU 16 3812317 3812317 single base substitution T A intron_variant MELA-AU 16 3813525 3813525 single base substitution G A downstream_gene_variant MELA-AU 16 3813525 3813525 single base substitution G A intron_variant MELA-AU 16 3813774 3813774 single base substitution T G downstream_gene_variant MELA-AU 16 3813774 3813774 single base substitution T G intron_variant MELA-AU 16 3813833 3813833 single base substitution G A downstream_gene_variant MELA-AU 16 3813833 3813833 single base substitution G A intron_variant MELA-AU 16 3816315 3816315 single base substitution G A downstream_gene_variant MELA-AU 16 3816315 3816315 single base substitution G A intron_variant MELA-AU 16 3817536 3817536 single base substitution G C exon_variant MELA-AU 16 3817536 3817536 single base substitution G C intron_variant MELA-AU 16 3817897 3817897 single base substitution T C exon_variant MELA-AU 16 3817897 3817897 single base substitution T C missense_variant D1025G 3074A>G MELA-AU 16 3817897 3817897 single base substitution T C missense_variant D987G 2960A>G MELA-AU 16 3817897 3817897 single base substitution T C upstream_gene_variant MELA-AU 16 3818968 3818968 single base substitution G A downstream_gene_variant MELA-AU 16 3818968 3818968 single base substitution G A intron_variant MELA-AU 16 3818968 3818968 single base substitution G A upstream_gene_variant MELA-AU 16 3818979 3818979 single base substitution C T downstream_gene_variant MELA-AU 16 3818979 3818979 single base substitution C T intron_variant MELA-AU 16 3818979 3818979 single base substitution C T upstream_gene_variant MELA-AU 16 3819211 3819212 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 3819211 3819212 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 16 3819211 3819212 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P1008L 3023CC>TT MELA-AU 16 3819211 3819212 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P970L 2909CC>TT MELA-AU 16 3819211 3819212 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 3819827 3819827 single base substitution G A downstream_gene_variant MELA-AU 16 3819827 3819827 single base substitution G A intron_variant MELA-AU 16 3819827 3819827 single base substitution G A upstream_gene_variant MELA-AU 16 3820515 3820515 single base substitution G A downstream_gene_variant MELA-AU 16 3820515 3820515 single base substitution G A intron_variant MELA-AU 16 3820515 3820515 single base substitution G A upstream_gene_variant MELA-AU 16 3820807 3820807 single base substitution G A downstream_gene_variant MELA-AU 16 3820807 3820807 single base substitution G A missense_variant P844S 2530C>T MELA-AU 16 3820807 3820807 single base substitution G A missense_variant P882S 2644C>T MELA-AU 16 3820807 3820807 single base substitution G A upstream_gene_variant MELA-AU 16 3821741 3821741 single base substitution G A downstream_gene_variant MELA-AU 16 3821741 3821741 single base substitution G A intron_variant MELA-AU 16 3821741 3821741 single base substitution G A upstream_gene_variant MELA-AU 16 3822417 3822417 insertion of <=200bp - AT downstream_gene_variant MELA-AU 16 3822417 3822417 insertion of <=200bp - AT intron_variant MELA-AU 16 3822417 3822417 insertion of <=200bp - AT upstream_gene_variant MELA-AU 16 3823673 3823673 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3823673 3823673 single base substitution G A downstream_gene_variant MELA-AU 16 3823673 3823673 single base substitution G A intron_variant MELA-AU 16 3823673 3823673 single base substitution G A upstream_gene_variant MELA-AU 16 3825580 3825580 single base substitution G A intron_variant MELA-AU 16 3825580 3825580 single base substitution G A upstream_gene_variant MELA-AU 16 3826268 3826268 single base substitution C T intron_variant MELA-AU 16 3826268 3826268 single base substitution C T upstream_gene_variant MELA-AU 16 3826282 3826282 single base substitution G A intron_variant MELA-AU 16 3826282 3826282 single base substitution G A upstream_gene_variant MELA-AU 16 3826934 3826934 single base substitution G A intron_variant MELA-AU 16 3826934 3826934 single base substitution G A upstream_gene_variant MELA-AU 16 3827509 3827509 single base substitution A C intron_variant MELA-AU 16 3827509 3827509 single base substitution A C upstream_gene_variant MELA-AU 16 3827544 3827544 single base substitution G A intron_variant MELA-AU 16 3827544 3827544 single base substitution G A upstream_gene_variant MELA-AU 16 3827906 3827906 single base substitution G A intron_variant MELA-AU 16 3827906 3827906 single base substitution G A upstream_gene_variant MELA-AU 16 3828033 3828034 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant QA134QT MELA-AU 16 3828033 3828034 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant QA46QT MELA-AU 16 3828033 3828034 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant QA659QT MELA-AU 16 3828033 3828034 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant QA697QT MELA-AU 16 3828033 3828034 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 3828789 3828789 single base substitution G A missense_variant P55L 164C>T MELA-AU 16 3828789 3828789 single base substitution G A missense_variant P580L 1739C>T MELA-AU 16 3828789 3828789 single base substitution G A missense_variant P618L 1853C>T MELA-AU 16 3828789 3828789 single base substitution G A upstream_gene_variant MELA-AU 16 3829040 3829040 single base substitution T C intron_variant MELA-AU 16 3829040 3829040 single base substitution T C upstream_gene_variant MELA-AU 16 3829502 3829502 single base substitution A G intron_variant MELA-AU 16 3829502 3829502 single base substitution A G upstream_gene_variant MELA-AU 16 3829783 3829783 single base substitution G A intron_variant MELA-AU 16 3829783 3829783 single base substitution G A upstream_gene_variant MELA-AU 16 3831280 3831280 single base substitution C T missense_variant G496E 1487G>A MELA-AU 16 3831280 3831280 single base substitution C T missense_variant G534E 1601G>A MELA-AU 16 3831280 3831280 single base substitution C T upstream_gene_variant MELA-AU 16 3831457 3831457 single base substitution G A intron_variant MELA-AU 16 3831457 3831457 single base substitution G A upstream_gene_variant MELA-AU 16 3831772 3831772 single base substitution G A intron_variant MELA-AU 16 3831772 3831772 single base substitution G A upstream_gene_variant MELA-AU 16 3832140 3832140 single base substitution G A intron_variant MELA-AU 16 3832140 3832140 single base substitution G A upstream_gene_variant MELA-AU 16 3833140 3833140 single base substitution A G intron_variant MELA-AU 16 3833140 3833140 single base substitution A G upstream_gene_variant MELA-AU 16 3835305 3835305 single base substitution C A intron_variant MELA-AU 16 3835305 3835305 single base substitution C A upstream_gene_variant MELA-AU 16 3835412 3835412 single base substitution C T intron_variant MELA-AU 16 3835412 3835412 single base substitution C T upstream_gene_variant MELA-AU 16 3835691 3835691 single base substitution G A intron_variant MELA-AU 16 3835691 3835691 single base substitution G A upstream_gene_variant MELA-AU 16 3836494 3836494 single base substitution G A intron_variant MELA-AU 16 3836604 3836604 single base substitution G A intron_variant MELA-AU 16 3836692 3836692 single base substitution G A intron_variant MELA-AU 16 3837051 3837051 single base substitution G A intron_variant MELA-AU 16 3837524 3837524 single base substitution A G intron_variant MELA-AU 16 3837627 3837627 single base substitution G A intron_variant MELA-AU 16 3837840 3837840 single base substitution C T intron_variant MELA-AU 16 3838284 3838284 single base substitution A T intron_variant MELA-AU 16 3839020 3839020 single base substitution T G intron_variant MELA-AU 16 3839898 3839898 single base substitution C T intron_variant MELA-AU 16 3840128 3840128 single base substitution G A intron_variant MELA-AU 16 3840696 3840696 single base substitution G A intron_variant MELA-AU 16 3841094 3841094 single base substitution G A intron_variant MELA-AU 16 3841130 3841130 single base substitution G A intron_variant MELA-AU 16 3841203 3841203 single base substitution G A intron_variant MELA-AU 16 3841240 3841240 single base substitution C T intron_variant MELA-AU 16 3841665 3841665 single base substitution G A intron_variant MELA-AU 16 3841809 3841809 single base substitution G A intron_variant MELA-AU 16 3842115 3842115 single base substitution G A intron_variant MELA-AU 16 3842301 3842301 deletion of <=200bp A - intron_variant MELA-AU 16 3842613 3842613 single base substitution A G intron_variant MELA-AU 16 3842862 3842862 single base substitution G A intron_variant MELA-AU 16 3843042 3843042 single base substitution G A intron_variant MELA-AU 16 3843116 3843116 single base substitution G A intron_variant MELA-AU 16 3844110 3844110 single base substitution C A intron_variant MELA-AU 16 3844509 3844509 single base substitution C T intron_variant MELA-AU 16 3845397 3845397 deletion of <=200bp A - intron_variant MELA-AU 16 3845860 3845860 single base substitution G A intron_variant MELA-AU 16 3846052 3846053 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 3846670 3846670 single base substitution G A intron_variant MELA-AU 16 3847699 3847699 single base substitution G A intron_variant MELA-AU 16 3847906 3847906 single base substitution G A intron_variant MELA-AU 16 3848037 3848037 single base substitution A G intron_variant MELA-AU 16 3848082 3848082 single base substitution G A intron_variant MELA-AU 16 3848209 3848209 single base substitution G A intron_variant MELA-AU 16 3848390 3848390 single base substitution G A intron_variant MELA-AU 16 3848870 3848870 single base substitution G A intron_variant MELA-AU 16 3849149 3849149 single base substitution G A intron_variant MELA-AU 16 3849346 3849346 single base substitution T C intron_variant MELA-AU 16 3849365 3849365 single base substitution G A intron_variant MELA-AU 16 3849517 3849517 single base substitution G A intron_variant MELA-AU 16 3849973 3849973 single base substitution G A intron_variant MELA-AU 16 3850570 3850570 single base substitution G A intron_variant MELA-AU 16 3850910 3850910 single base substitution G A intron_variant MELA-AU 16 3852437 3852437 single base substitution C T intron_variant MELA-AU 16 3853057 3853057 single base substitution G A intron_variant MELA-AU 16 3853158 3853158 single base substitution G A intron_variant MELA-AU 16 3853627 3853627 single base substitution G A intron_variant MELA-AU 16 3854586 3854586 single base substitution C T intron_variant MELA-AU 16 3854826 3854826 single base substitution G A intron_variant MELA-AU 16 3854925 3854925 single base substitution G A intron_variant MELA-AU 16 3856019 3856019 single base substitution G A intron_variant MELA-AU 16 3856430 3856430 single base substitution G A intron_variant MELA-AU 16 3856673 3856674 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3857740 3857740 single base substitution G A intron_variant MELA-AU 16 3858160 3858160 single base substitution G A intron_variant MELA-AU 16 3858481 3858481 single base substitution G A intron_variant MELA-AU 16 3858699 3858699 single base substitution G A intron_variant MELA-AU 16 3861487 3861487 single base substitution G A intron_variant MELA-AU 16 3861984 3861984 single base substitution G A intron_variant MELA-AU 16 3862314 3862314 single base substitution G A intron_variant MELA-AU 16 3862553 3862553 single base substitution G A intron_variant MELA-AU 16 3862897 3862897 single base substitution C T intron_variant MELA-AU 16 3863069 3863069 single base substitution C T intron_variant MELA-AU 16 3863775 3863775 single base substitution G A intron_variant MELA-AU 16 3863851 3863851 single base substitution T A intron_variant MELA-AU 16 3865517 3865517 single base substitution G A intron_variant MELA-AU 16 3865521 3865521 single base substitution G A intron_variant MELA-AU 16 3867379 3867379 single base substitution G A intron_variant MELA-AU 16 3867438 3867438 single base substitution A T intron_variant MELA-AU 16 3867784 3867784 single base substitution G A intron_variant MELA-AU 16 3867817 3867817 single base substitution G A intron_variant MELA-AU 16 3867837 3867837 single base substitution G A intron_variant MELA-AU 16 3867917 3867917 single base substitution G A intron_variant MELA-AU 16 3868096 3868096 single base substitution G A intron_variant MELA-AU 16 3868287 3868287 single base substitution T C intron_variant MELA-AU 16 3868582 3868582 single base substitution C T intron_variant MELA-AU 16 3868976 3868976 single base substitution G A intron_variant MELA-AU 16 3871129 3871129 single base substitution C T intron_variant MELA-AU 16 3871261 3871261 single base substitution G A intron_variant MELA-AU 16 3871276 3871276 single base substitution C T intron_variant MELA-AU 16 3871454 3871454 single base substitution G C intron_variant MELA-AU 16 3871852 3871852 single base substitution G A intron_variant MELA-AU 16 3872090 3872090 single base substitution G A intron_variant MELA-AU 16 3872471 3872471 single base substitution G A intron_variant MELA-AU 16 3872868 3872868 single base substitution G A intron_variant MELA-AU 16 3872927 3872927 single base substitution G A intron_variant MELA-AU 16 3872981 3872981 single base substitution C T intron_variant MELA-AU 16 3873338 3873338 single base substitution A G intron_variant MELA-AU 16 3874203 3874203 single base substitution G A intron_variant MELA-AU 16 3874322 3874322 single base substitution G A intron_variant MELA-AU 16 3875682 3875682 single base substitution T C intron_variant MELA-AU 16 3876641 3876641 single base substitution G A intron_variant MELA-AU 16 3878322 3878322 single base substitution A G intron_variant MELA-AU 16 3878832 3878832 single base substitution A G intron_variant MELA-AU 16 3878861 3878861 single base substitution G A intron_variant MELA-AU 16 3879114 3879114 single base substitution G A intron_variant MELA-AU 16 3879222 3879222 single base substitution G A intron_variant MELA-AU 16 3879292 3879292 single base substitution G A intron_variant MELA-AU 16 3880322 3880322 single base substitution C T intron_variant MELA-AU 16 3880346 3880346 single base substitution G A intron_variant MELA-AU 16 3880488 3880488 single base substitution G A intron_variant MELA-AU 16 3880839 3880839 single base substitution G A intron_variant MELA-AU 16 3880886 3880886 single base substitution G A intron_variant MELA-AU 16 3881009 3881009 single base substitution A G intron_variant MELA-AU 16 3881419 3881419 insertion of <=200bp - A intron_variant MELA-AU 16 3881509 3881509 single base substitution C T intron_variant MELA-AU 16 3882287 3882287 single base substitution G A intron_variant MELA-AU 16 3882811 3882811 single base substitution G A intron_variant MELA-AU 16 3883791 3883791 single base substitution C T intron_variant MELA-AU 16 3884018 3884018 single base substitution G A intron_variant MELA-AU 16 3884745 3884745 single base substitution G A intron_variant MELA-AU 16 3885260 3885260 single base substitution G A intron_variant MELA-AU 16 3885308 3885308 single base substitution G T intron_variant MELA-AU 16 3885773 3885773 single base substitution G A intron_variant MELA-AU 16 3886491 3886491 single base substitution G A intron_variant MELA-AU 16 3886512 3886512 single base substitution G A intron_variant MELA-AU 16 3886650 3886650 single base substitution A T intron_variant MELA-AU 16 3886842 3886842 single base substitution G A intron_variant MELA-AU 16 3887208 3887208 single base substitution G A intron_variant MELA-AU 16 3887446 3887446 single base substitution G A intron_variant MELA-AU 16 3887653 3887653 single base substitution A G intron_variant MELA-AU 16 3888666 3888666 single base substitution G A intron_variant MELA-AU 16 3889019 3889019 single base substitution A G intron_variant MELA-AU 16 3891407 3891407 single base substitution G A intron_variant MELA-AU 16 3891463 3891463 single base substitution G A intron_variant MELA-AU 16 3893702 3893702 single base substitution T A intron_variant MELA-AU 16 3893817 3893817 single base substitution T C intron_variant MELA-AU 16 3893827 3893827 single base substitution T G intron_variant MELA-AU 16 3895107 3895107 single base substitution T C intron_variant MELA-AU 16 3896189 3896189 single base substitution G A intron_variant MELA-AU 16 3896753 3896753 single base substitution G A intron_variant MELA-AU 16 3897814 3897814 single base substitution G A intron_variant MELA-AU 16 3898066 3898066 single base substitution G A intron_variant MELA-AU 16 3898799 3898799 single base substitution C T intron_variant MELA-AU 16 3899635 3899635 single base substitution G T intron_variant MELA-AU 16 3899990 3899990 single base substitution C T intron_variant MELA-AU 16 3900243 3900244 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3900663 3900663 single base substitution G A missense_variant P145S 433C>T MELA-AU 16 3901631 3901632 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3901966 3901966 single base substitution G A intron_variant MELA-AU 16 3902024 3902024 single base substitution G A intron_variant MELA-AU 16 3902173 3902173 single base substitution T G intron_variant MELA-AU 16 3902264 3902264 single base substitution G A intron_variant MELA-AU 16 3902305 3902305 single base substitution G A intron_variant MELA-AU 16 3902335 3902335 single base substitution A G intron_variant MELA-AU 16 3903963 3903963 insertion of <=200bp - AC intron_variant MELA-AU 16 3904020 3904020 single base substitution T C intron_variant MELA-AU 16 3904859 3904859 single base substitution G A intron_variant MELA-AU 16 3905093 3905093 single base substitution G A intron_variant MELA-AU 16 3906109 3906109 deletion of <=200bp C - intron_variant MELA-AU 16 3906425 3906425 single base substitution G A intron_variant MELA-AU 16 3906678 3906678 single base substitution C T intron_variant MELA-AU 16 3907923 3907923 single base substitution T C intron_variant MELA-AU 16 3908846 3908846 single base substitution G A intron_variant MELA-AU 16 3909257 3909257 single base substitution G A intron_variant MELA-AU 16 3909730 3909730 single base substitution A C intron_variant MELA-AU 16 3909945 3909946 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3909946 3909946 single base substitution G A intron_variant MELA-AU 16 3910344 3910344 single base substitution G A intron_variant MELA-AU 16 3910984 3910984 single base substitution G A intron_variant MELA-AU 16 3911053 3911053 single base substitution C T intron_variant MELA-AU 16 3912204 3912204 single base substitution G C intron_variant MELA-AU 16 3912374 3912374 single base substitution C T intron_variant MELA-AU 16 3912513 3912513 single base substitution T C intron_variant MELA-AU 16 3912540 3912540 single base substitution T C intron_variant MELA-AU 16 3912710 3912710 single base substitution G A intron_variant MELA-AU 16 3912943 3912943 single base substitution G A intron_variant MELA-AU 16 3913909 3913909 single base substitution G A intron_variant MELA-AU 16 3914783 3914783 single base substitution C A intron_variant MELA-AU 16 3915905 3915905 single base substitution G A intron_variant MELA-AU 16 3915945 3915945 single base substitution G A intron_variant MELA-AU 16 3916800 3916800 single base substitution G A intron_variant MELA-AU 16 3916901 3916902 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 3916928 3916928 single base substitution G A intron_variant MELA-AU 16 3917018 3917018 single base substitution G A intron_variant MELA-AU 16 3917273 3917273 single base substitution G A intron_variant MELA-AU 16 3917487 3917487 single base substitution C T intron_variant MELA-AU 16 3917924 3917924 single base substitution C T intron_variant MELA-AU 16 3918983 3918983 single base substitution G T intron_variant MELA-AU 16 3919223 3919223 single base substitution C T intron_variant MELA-AU 16 3919464 3919464 single base substitution G A intron_variant MELA-AU 16 3919895 3919896 multiple base substitution (>=2bp and <=200bp) CA AT intron_variant MELA-AU 16 3920067 3920067 single base substitution A T intron_variant MELA-AU 16 3920235 3920235 single base substitution A T intron_variant MELA-AU 16 3920756 3920756 single base substitution G A intron_variant MELA-AU 16 3921720 3921720 single base substitution G A intron_variant MELA-AU 16 3922526 3922526 single base substitution A T intron_variant MELA-AU 16 3922802 3922802 single base substitution G A intron_variant MELA-AU 16 3923677 3923677 single base substitution T C intron_variant MELA-AU 16 3923971 3923971 single base substitution G A intron_variant MELA-AU 16 3924209 3924209 single base substitution G A intron_variant MELA-AU 16 3924862 3924863 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3926143 3926143 single base substitution G A intron_variant MELA-AU 16 3927904 3927904 single base substitution G A intron_variant MELA-AU 16 3927924 3927924 single base substitution G A intron_variant MELA-AU 16 3928049 3928068 deletion of <=200bp TACATATAAGGACATGCCTT - intron_variant MELA-AU 16 3928692 3928692 single base substitution G A intron_variant MELA-AU 16 3928906 3928907 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 16 3930823 3930823 single base substitution C T upstream_gene_variant MELA-AU 16 3931428 3931428 single base substitution C T upstream_gene_variant MELA-AU 16 3932517 3932517 single base substitution C T upstream_gene_variant MELA-AU 16 3932560 3932560 single base substitution C T upstream_gene_variant MELA-AU 16 3932676 3932676 single base substitution C T upstream_gene_variant MELA-AU 16 3932773 3932773 single base substitution C T upstream_gene_variant MELA-AU 16 3933201 3933202 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 3933393 3933393 single base substitution C T upstream_gene_variant MELA-AU 16 3933644 3933644 single base substitution G A upstream_gene_variant MELA-AU 16 3933698 3933698 single base substitution G A upstream_gene_variant MELA-AU 16 3934555 3934555 single base substitution A T upstream_gene_variant MELA-AU 16 3934656 3934656 single base substitution C T upstream_gene_variant MELA-AU 16 3934692 3934692 single base substitution C T upstream_gene_variant MELA-AU 16 3934728 3934728 single base substitution C T upstream_gene_variant MELA-AU 16 3934899 3934899 single base substitution C T upstream_gene_variant MELA-AU 16 3935245 3935245 single base substitution G A upstream_gene_variant MELA-AU 16 3935623 3935623 single base substitution C T upstream_gene_variant ORCA-IN 16 3777950 3777950 single base substitution C T downstream_gene_variant ORCA-IN 16 3777950 3777950 single base substitution C T synonymous_variant R2328R 6984G>A ORCA-IN 16 3777950 3777950 single base substitution C T synonymous_variant R2366R 7098G>A ORCA-IN 16 3778982 3778982 single base substitution C T downstream_gene_variant ORCA-IN 16 3778982 3778982 single base substitution C T synonymous_variant Q1984Q 5952G>A ORCA-IN 16 3778982 3778982 single base substitution C T synonymous_variant Q2022Q 6066G>A ORCA-IN 16 3779355 3779355 single base substitution C A downstream_gene_variant ORCA-IN 16 3779355 3779355 single base substitution C A missense_variant S1860I 5579G>T ORCA-IN 16 3779355 3779355 single base substitution C A missense_variant S1898I 5693G>T ORCA-IN 16 3779608 3779608 single base substitution C T downstream_gene_variant ORCA-IN 16 3779608 3779608 single base substitution C T missense_variant G1776R 5326G>A ORCA-IN 16 3779608 3779608 single base substitution C T missense_variant G1814R 5440G>A ORCA-IN 16 3788618 3788618 single base substitution G A downstream_gene_variant ORCA-IN 16 3788618 3788618 single base substitution G A intron_variant ORCA-IN 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T ORCA-IN 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T ORCA-IN 16 3788618 3788618 single base substitution G A upstream_gene_variant ORCA-IN 16 3798105 3798105 single base substitution A C intron_variant ORCA-IN 16 3798105 3798105 single base substitution A C upstream_gene_variant ORCA-IN 16 3849110 3849110 single base substitution G A intron_variant ORCA-IN 16 3854033 3854033 single base substitution G A intron_variant ORCA-IN 16 3879264 3879264 single base substitution G A intron_variant ORCA-IN 16 3931944 3931944 single base substitution T C upstream_gene_variant OV-AU 16 3770723 3770723 single base substitution G A downstream_gene_variant OV-AU 16 3773128 3773128 single base substitution C G downstream_gene_variant OV-AU 16 3776612 3776612 single base substitution T G 3_prime_UTR_variant OV-AU 16 3776612 3776612 single base substitution T G downstream_gene_variant OV-AU 16 3777833 3777833 single base substitution C A downstream_gene_variant OV-AU 16 3777833 3777833 single base substitution C A missense_variant Q2367H 7101G>T OV-AU 16 3777833 3777833 single base substitution C A missense_variant Q2405H 7215G>T OV-AU 16 3788952 3788952 single base substitution C T downstream_gene_variant OV-AU 16 3788952 3788952 single base substitution C T intron_variant OV-AU 16 3788952 3788952 single base substitution C T upstream_gene_variant OV-AU 16 3799917 3799917 single base substitution T G intron_variant OV-AU 16 3799917 3799917 single base substitution T G upstream_gene_variant OV-AU 16 3802653 3802653 single base substitution T C intron_variant OV-AU 16 3802653 3802653 single base substitution T C upstream_gene_variant OV-AU 16 3804435 3804435 single base substitution C G intron_variant OV-AU 16 3804435 3804435 single base substitution C G upstream_gene_variant OV-AU 16 3812107 3812107 single base substitution A T intron_variant OV-AU 16 3816152 3816152 single base substitution C G downstream_gene_variant OV-AU 16 3816152 3816152 single base substitution C G intron_variant OV-AU 16 3818697 3818697 single base substitution A C downstream_gene_variant OV-AU 16 3818697 3818697 single base substitution A C intron_variant OV-AU 16 3818697 3818697 single base substitution A C upstream_gene_variant OV-AU 16 3835353 3835353 single base substitution G A intron_variant OV-AU 16 3835353 3835353 single base substitution G A upstream_gene_variant OV-AU 16 3835797 3835797 single base substitution G C intron_variant OV-AU 16 3835797 3835797 single base substitution G C upstream_gene_variant OV-AU 16 3847262 3847262 single base substitution T C intron_variant OV-AU 16 3851803 3851803 single base substitution T C intron_variant OV-AU 16 3852194 3852194 single base substitution A C intron_variant OV-AU 16 3852365 3852365 single base substitution T A intron_variant OV-AU 16 3853167 3853167 single base substitution T A intron_variant OV-AU 16 3854068 3854068 single base substitution G A intron_variant OV-AU 16 3855258 3855258 single base substitution A G intron_variant OV-AU 16 3860790 3860790 single base substitution A T intron_variant OV-AU 16 3860791 3860791 single base substitution A G intron_variant OV-AU 16 3864330 3864330 single base substitution C T intron_variant OV-AU 16 3866248 3866248 single base substitution G C intron_variant OV-AU 16 3870150 3870150 single base substitution G C intron_variant OV-AU 16 3873272 3873272 single base substitution G A intron_variant OV-AU 16 3873788 3873788 single base substitution T C intron_variant OV-AU 16 3879805 3879805 single base substitution A T intron_variant OV-AU 16 3904675 3904675 single base substitution C T intron_variant OV-AU 16 3906310 3906310 single base substitution A T intron_variant OV-AU 16 3908276 3908276 single base substitution A T intron_variant OV-AU 16 3909548 3909548 single base substitution T C intron_variant OV-AU 16 3911594 3911594 single base substitution T C intron_variant OV-AU 16 3926784 3926784 single base substitution A G intron_variant OV-AU 16 3931402 3931402 single base substitution T G upstream_gene_variant OV-US 16 3790520 3790520 single base substitution A G exon_variant OV-US 16 3790520 3790520 single base substitution A G missense_variant L106S 317T>C OV-US 16 3790520 3790520 single base substitution A G missense_variant L1300S 3899T>C OV-US 16 3790520 3790520 single base substitution A G missense_variant L1338S 4013T>C OV-US 16 3790520 3790520 single base substitution A G missense_variant L211S 632T>C OV-US 16 3790520 3790520 single base substitution A G upstream_gene_variant OV-US 16 3820936 3820942 deletion of <=200bp GAGGCCC - downstream_gene_variant OV-US 16 3820936 3820942 deletion of <=200bp GAGGCCC - frameshift_variant GPQ799 OV-US 16 3820936 3820942 deletion of <=200bp GAGGCCC - frameshift_variant GPQ837 OV-US 16 3820936 3820942 deletion of <=200bp GAGGCCC - upstream_gene_variant PACA-AU 16 3773049 3773049 single base substitution G A downstream_gene_variant PACA-AU 16 3778207 3778207 single base substitution C T downstream_gene_variant PACA-AU 16 3778207 3778207 single base substitution C T missense_variant A2243T 6727G>A PACA-AU 16 3778207 3778207 single base substitution C T missense_variant A2281T 6841G>A PACA-AU 16 3778303 3778305 deletion of <=200bp GCT - disruptive_inframe_deletion QR2210R PACA-AU 16 3778303 3778305 deletion of <=200bp GCT - disruptive_inframe_deletion QR2248R PACA-AU 16 3778303 3778305 deletion of <=200bp GCT - downstream_gene_variant PACA-AU 16 3779705 3779705 single base substitution G A downstream_gene_variant PACA-AU 16 3779705 3779705 single base substitution G A synonymous_variant H1743H 5229C>T PACA-AU 16 3779705 3779705 single base substitution G A synonymous_variant H1781H 5343C>T PACA-AU 16 3779781 3779781 single base substitution T C downstream_gene_variant PACA-AU 16 3779781 3779781 single base substitution T C missense_variant Q1718R 5153A>G PACA-AU 16 3779781 3779781 single base substitution T C missense_variant Q1756R 5267A>G PACA-AU 16 3781850 3781850 single base substitution T C downstream_gene_variant PACA-AU 16 3781850 3781850 single base substitution T C missense_variant K1568R 4703A>G PACA-AU 16 3781850 3781850 single base substitution T C missense_variant K1606R 4817A>G PACA-AU 16 3783662 3783662 single base substitution G T downstream_gene_variant PACA-AU 16 3783662 3783662 single base substitution G T intron_variant PACA-AU 16 3790706 3790706 single base substitution C T exon_variant PACA-AU 16 3790706 3790706 single base substitution C T intron_variant PACA-AU 16 3790706 3790706 single base substitution C T upstream_gene_variant PACA-AU 16 3792038 3792038 single base substitution C A exon_variant PACA-AU 16 3792038 3792038 single base substitution C A intron_variant PACA-AU 16 3794563 3794563 single base substitution G A intron_variant PACA-AU 16 3794563 3794563 single base substitution G A upstream_gene_variant PACA-AU 16 3795018 3795018 single base substitution C T intron_variant PACA-AU 16 3795018 3795018 single base substitution C T upstream_gene_variant PACA-AU 16 3806886 3806886 single base substitution G A intron_variant PACA-AU 16 3809967 3809967 single base substitution C T intron_variant PACA-AU 16 3822042 3822042 single base substitution T C downstream_gene_variant PACA-AU 16 3822042 3822042 single base substitution T C intron_variant PACA-AU 16 3822042 3822042 single base substitution T C upstream_gene_variant PACA-AU 16 3827829 3827829 single base substitution C T intron_variant PACA-AU 16 3827829 3827829 single base substitution C T upstream_gene_variant PACA-AU 16 3832988 3832988 single base substitution G A intron_variant PACA-AU 16 3832988 3832988 single base substitution G A upstream_gene_variant PACA-AU 16 3836455 3836455 single base substitution T C intron_variant PACA-AU 16 3836599 3836599 single base substitution A G intron_variant PACA-AU 16 3837515 3837515 single base substitution G T intron_variant PACA-AU 16 3841334 3841334 single base substitution C T intron_variant PACA-AU 16 3843207 3843241 deletion of <=200bp ACTTCCTGGAGCACCTGACTGTCGTCGCGTGGGGA - intron_variant PACA-AU 16 3848508 3848508 single base substitution T G intron_variant PACA-AU 16 3848710 3848710 single base substitution C G intron_variant PACA-AU 16 3853167 3853167 single base substitution T A intron_variant PACA-AU 16 3854407 3854407 deletion of <=200bp T - intron_variant PACA-AU 16 3854769 3854769 insertion of <=200bp - A intron_variant PACA-AU 16 3864508 3864508 single base substitution C G intron_variant PACA-AU 16 3866222 3866222 single base substitution C T intron_variant PACA-AU 16 3877537 3877537 single base substitution C T intron_variant PACA-AU 16 3877553 3877553 single base substitution C T intron_variant PACA-AU 16 3879792 3879792 single base substitution G C intron_variant PACA-AU 16 3881324 3881324 single base substitution A T intron_variant PACA-AU 16 3883228 3883228 single base substitution A G intron_variant PACA-AU 16 3884109 3884109 deletion of <=200bp G - intron_variant PACA-AU 16 3886853 3886853 single base substitution A G intron_variant PACA-AU 16 3888756 3888756 single base substitution C T intron_variant PACA-AU 16 3889074 3889074 single base substitution T A intron_variant PACA-AU 16 3896265 3896265 single base substitution G C intron_variant PACA-AU 16 3896592 3896592 single base substitution G A intron_variant PACA-AU 16 3897352 3897352 single base substitution C A intron_variant PACA-AU 16 3898519 3898519 single base substitution C A intron_variant PACA-AU 16 3899749 3899749 single base substitution C G intron_variant PACA-AU 16 3902949 3902949 single base substitution A C intron_variant PACA-AU 16 3903428 3903428 single base substitution G A intron_variant PACA-AU 16 3903580 3903580 single base substitution C A intron_variant PACA-AU 16 3903584 3903584 single base substitution C T intron_variant PACA-AU 16 3903921 3903921 single base substitution A G intron_variant PACA-AU 16 3905390 3905390 single base substitution A T intron_variant PACA-AU 16 3906494 3906494 single base substitution T A intron_variant PACA-AU 16 3910109 3910109 single base substitution C G intron_variant PACA-AU 16 3910562 3910562 single base substitution A C intron_variant PACA-AU 16 3911704 3911704 single base substitution C T intron_variant PACA-AU 16 3912121 3912121 single base substitution G T intron_variant PACA-AU 16 3915468 3915468 single base substitution G C intron_variant PACA-AU 16 3916639 3916639 single base substitution A G intron_variant PACA-AU 16 3917056 3917056 single base substitution C T intron_variant PACA-AU 16 3920571 3920571 single base substitution G T intron_variant PACA-AU 16 3921337 3921337 single base substitution C T intron_variant PACA-AU 16 3923631 3923631 single base substitution C T intron_variant PACA-AU 16 3925860 3925860 single base substitution C G intron_variant PACA-CA 16 3771307 3771307 single base substitution C T downstream_gene_variant PACA-CA 16 3772274 3772274 single base substitution C T downstream_gene_variant PACA-CA 16 3772422 3772422 single base substitution C T downstream_gene_variant PACA-CA 16 3773034 3773034 single base substitution C T downstream_gene_variant PACA-CA 16 3781341 3781341 single base substitution T C downstream_gene_variant PACA-CA 16 3781341 3781341 single base substitution T C missense_variant H1637R 4910A>G PACA-CA 16 3781341 3781341 single base substitution T C missense_variant H1675R 5024A>G PACA-CA 16 3782377 3782377 single base substitution G A downstream_gene_variant PACA-CA 16 3782377 3782377 single base substitution G A intron_variant PACA-CA 16 3791766 3791766 single base substitution C A exon_variant PACA-CA 16 3791766 3791766 single base substitution C A intron_variant PACA-CA 16 3791766 3791766 single base substitution C A upstream_gene_variant PACA-CA 16 3800538 3800538 insertion of <=200bp - C intron_variant PACA-CA 16 3800538 3800538 insertion of <=200bp - C upstream_gene_variant PACA-CA 16 3806637 3806637 single base substitution G A intron_variant PACA-CA 16 3806637 3806637 single base substitution G A upstream_gene_variant PACA-CA 16 3808348 3808348 single base substitution C A intron_variant PACA-CA 16 3816588 3816588 single base substitution G A downstream_gene_variant PACA-CA 16 3816588 3816588 single base substitution G A intron_variant PACA-CA 16 3821690 3821690 single base substitution T C downstream_gene_variant PACA-CA 16 3821690 3821690 single base substitution T C intron_variant PACA-CA 16 3821690 3821690 single base substitution T C upstream_gene_variant PACA-CA 16 3825143 3825143 single base substitution C G intron_variant PACA-CA 16 3825143 3825143 single base substitution C G upstream_gene_variant PACA-CA 16 3826814 3826814 single base substitution C T intron_variant PACA-CA 16 3826814 3826814 single base substitution C T upstream_gene_variant PACA-CA 16 3835040 3835040 single base substitution C T intron_variant PACA-CA 16 3835040 3835040 single base substitution C T upstream_gene_variant PACA-CA 16 3835335 3835335 single base substitution G A intron_variant PACA-CA 16 3835335 3835335 single base substitution G A upstream_gene_variant PACA-CA 16 3839433 3839433 single base substitution G T intron_variant PACA-CA 16 3841329 3841329 single base substitution C T intron_variant PACA-CA 16 3853167 3853167 single base substitution T A intron_variant PACA-CA 16 3858673 3858673 single base substitution A G intron_variant PACA-CA 16 3861934 3861934 single base substitution T A intron_variant PACA-CA 16 3864871 3864871 single base substitution C G intron_variant PACA-CA 16 3867520 3867520 insertion of <=200bp - A intron_variant PACA-CA 16 3874680 3874680 single base substitution C T intron_variant PACA-CA 16 3875603 3875622 deletion of <=200bp GAAAATGAGATCTACATCAC - intron_variant PACA-CA 16 3878402 3878402 single base substitution T A intron_variant PACA-CA 16 3881124 3881124 single base substitution T C intron_variant PACA-CA 16 3883424 3883424 deletion of <=200bp A - intron_variant PACA-CA 16 3884745 3884745 single base substitution G A intron_variant PACA-CA 16 3886149 3886149 single base substitution A T intron_variant PACA-CA 16 3886894 3886894 single base substitution A C intron_variant PACA-CA 16 3887795 3887795 single base substitution T C intron_variant PACA-CA 16 3890633 3890635 deletion of <=200bp GAG - intron_variant PACA-CA 16 3893267 3893267 deletion of <=200bp T - intron_variant PACA-CA 16 3893555 3893555 single base substitution G T intron_variant PACA-CA 16 3893604 3893604 single base substitution T A intron_variant PACA-CA 16 3893605 3893605 single base substitution A T intron_variant PACA-CA 16 3893754 3893754 deletion of <=200bp A - intron_variant PACA-CA 16 3894493 3894493 single base substitution G A intron_variant PACA-CA 16 3894969 3894969 single base substitution G A intron_variant PACA-CA 16 3895039 3895039 single base substitution A C intron_variant PACA-CA 16 3897342 3897342 single base substitution A T intron_variant PACA-CA 16 3899227 3899227 insertion of <=200bp - TCCT intron_variant PACA-CA 16 3899753 3899753 single base substitution T C intron_variant PACA-CA 16 3901671 3901671 single base substitution C T intron_variant PACA-CA 16 3901955 3901955 single base substitution C T intron_variant PACA-CA 16 3906335 3906335 single base substitution T C intron_variant PACA-CA 16 3906494 3906494 single base substitution T A intron_variant PACA-CA 16 3911586 3911586 single base substitution A G intron_variant PACA-CA 16 3914668 3914668 single base substitution A G intron_variant PACA-CA 16 3915017 3915017 single base substitution G A intron_variant PACA-CA 16 3918355 3918355 single base substitution G A intron_variant PACA-CA 16 3920390 3920390 single base substitution A C intron_variant PACA-CA 16 3920523 3920523 single base substitution T A intron_variant PACA-CA 16 3920794 3920794 single base substitution A G intron_variant PACA-CA 16 3923347 3923347 single base substitution A C intron_variant PACA-CA 16 3924397 3924404 deletion of <=200bp TGCTCAGA - intron_variant PACA-CA 16 3926215 3926215 single base substitution A T intron_variant PACA-CA 16 3929519 3929519 single base substitution G A intron_variant PACA-CA 16 3932145 3932145 single base substitution C T upstream_gene_variant PACA-CA 16 3933029 3933029 single base substitution G A upstream_gene_variant PAEN-AU 16 3773398 3773398 single base substitution A C downstream_gene_variant PAEN-AU 16 3813649 3813649 single base substitution G C downstream_gene_variant PAEN-AU 16 3813649 3813649 single base substitution G C intron_variant PAEN-AU 16 3818987 3818987 single base substitution T G downstream_gene_variant PAEN-AU 16 3818987 3818987 single base substitution T G intron_variant PAEN-AU 16 3818987 3818987 single base substitution T G upstream_gene_variant PAEN-AU 16 3832375 3832375 single base substitution G A intron_variant PAEN-AU 16 3832375 3832375 single base substitution G A upstream_gene_variant PAEN-AU 16 3874694 3874694 single base substitution C T intron_variant PAEN-AU 16 3886807 3886812 deletion of <=200bp CATACA - intron_variant PAEN-AU 16 3898094 3898094 single base substitution C A intron_variant PAEN-IT 16 3857911 3857911 single base substitution C A intron_variant PAEN-IT 16 3880536 3880536 single base substitution A C intron_variant PAEN-IT 16 3925632 3925632 single base substitution T C intron_variant PBCA-DE 16 3771635 3771635 single base substitution G A downstream_gene_variant PBCA-DE 16 3779665 3779665 single base substitution A G downstream_gene_variant PBCA-DE 16 3779665 3779665 single base substitution A G missense_variant C1757R 5269T>C PBCA-DE 16 3779665 3779665 single base substitution A G missense_variant C1795R 5383T>C PBCA-DE 16 3781324 3781326 deletion of <=200bp AGG - disruptive_inframe_deletion SL1642L PBCA-DE 16 3781324 3781326 deletion of <=200bp AGG - disruptive_inframe_deletion SL1680L PBCA-DE 16 3781324 3781326 deletion of <=200bp AGG - downstream_gene_variant PBCA-DE 16 3782711 3782711 insertion of <=200bp - T downstream_gene_variant PBCA-DE 16 3782711 3782711 insertion of <=200bp - T intron_variant PBCA-DE 16 3786740 3786740 single base substitution G T downstream_gene_variant PBCA-DE 16 3786740 3786740 single base substitution G T exon_variant PBCA-DE 16 3786740 3786740 single base substitution G T missense_variant Q1453K 4357C>A PBCA-DE 16 3786740 3786740 single base substitution G T missense_variant Q1491K 4471C>A PBCA-DE 16 3786764 3786764 single base substitution T A downstream_gene_variant PBCA-DE 16 3786764 3786764 single base substitution T A exon_variant PBCA-DE 16 3786764 3786764 single base substitution T A missense_variant I1445F 4333A>T PBCA-DE 16 3786764 3786764 single base substitution T A missense_variant I1483F 4447A>T PBCA-DE 16 3788617 3788617 single base substitution C A downstream_gene_variant PBCA-DE 16 3788617 3788617 single base substitution C A intron_variant PBCA-DE 16 3788617 3788617 single base substitution C A missense_variant R1408L 4223G>T PBCA-DE 16 3788617 3788617 single base substitution C A missense_variant R1446L 4337G>T PBCA-DE 16 3788617 3788617 single base substitution C A upstream_gene_variant PBCA-DE 16 3788618 3788618 single base substitution G A downstream_gene_variant PBCA-DE 16 3788618 3788618 single base substitution G A intron_variant PBCA-DE 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T PBCA-DE 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T PBCA-DE 16 3788618 3788618 single base substitution G A upstream_gene_variant PBCA-DE 16 3794922 3794922 single base substitution G A exon_variant PBCA-DE 16 3794922 3794922 single base substitution G A stop_gained R1281* 3841C>T PBCA-DE 16 3794922 3794922 single base substitution G A stop_gained R1319* 3955C>T PBCA-DE 16 3794922 3794922 single base substitution G A stop_gained R192* 574C>T PBCA-DE 16 3794922 3794922 single base substitution G A stop_gained R87* 259C>T PBCA-DE 16 3794922 3794922 single base substitution G A upstream_gene_variant PBCA-DE 16 3795533 3795533 single base substitution T C exon_variant PBCA-DE 16 3795533 3795533 single base substitution T C intron_variant PBCA-DE 16 3795533 3795533 single base substitution T C upstream_gene_variant PBCA-DE 16 3804540 3804540 single base substitution T A intron_variant PBCA-DE 16 3804540 3804540 single base substitution T A upstream_gene_variant PBCA-DE 16 3807820 3807820 single base substitution C T intron_variant PBCA-DE 16 3807820 3807820 single base substitution C T missense_variant C1162Y 3485G>A PBCA-DE 16 3807820 3807820 single base substitution C T missense_variant C1200Y 3599G>A PBCA-DE 16 3809421 3809421 single base substitution C T intron_variant PBCA-DE 16 3809481 3809481 single base substitution G A intron_variant PBCA-DE 16 3823018 3823018 single base substitution G A downstream_gene_variant PBCA-DE 16 3823018 3823018 single base substitution G A intron_variant PBCA-DE 16 3823018 3823018 single base substitution G A upstream_gene_variant PBCA-DE 16 3825362 3825362 single base substitution C T intron_variant PBCA-DE 16 3825362 3825362 single base substitution C T upstream_gene_variant PBCA-DE 16 3828164 3828164 single base substitution A T stop_gained L3* 8T>A PBCA-DE 16 3828164 3828164 single base substitution A T stop_gained L616* 1847T>A PBCA-DE 16 3828164 3828164 single base substitution A T stop_gained L654* 1961T>A PBCA-DE 16 3828164 3828164 single base substitution A T stop_gained L91* 272T>A PBCA-DE 16 3828164 3828164 single base substitution A T upstream_gene_variant PBCA-DE 16 3830388 3830388 single base substitution T C intron_variant PBCA-DE 16 3830388 3830388 single base substitution T C upstream_gene_variant PBCA-DE 16 3846675 3846675 single base substitution A G intron_variant PBCA-DE 16 3863973 3863973 single base substitution A G intron_variant PBCA-DE 16 3864166 3864167 deletion of <=200bp GT - intron_variant PBCA-DE 16 3870627 3870627 single base substitution C T intron_variant PBCA-DE 16 3891880 3891880 single base substitution T G intron_variant PBCA-DE 16 3901631 3901631 insertion of <=200bp - CAT intron_variant PBCA-DE 16 3902316 3902316 single base substitution C T intron_variant PBCA-DE 16 3920612 3920612 single base substitution C G intron_variant PBCA-DE 16 3930764 3930764 single base substitution A G upstream_gene_variant PBCA-DE 16 3930770 3930770 single base substitution T G upstream_gene_variant PBCA-DE 16 3931946 3931946 single base substitution A C upstream_gene_variant PRAD-CA 16 3791304 3791304 single base substitution T A exon_variant PRAD-CA 16 3791304 3791304 single base substitution T A intron_variant PRAD-CA 16 3791304 3791304 single base substitution T A upstream_gene_variant PRAD-CA 16 3801263 3801263 single base substitution C T intron_variant PRAD-CA 16 3821820 3821820 single base substitution T A downstream_gene_variant PRAD-CA 16 3821820 3821820 single base substitution T A intron_variant PRAD-CA 16 3821820 3821820 single base substitution T A upstream_gene_variant PRAD-CA 16 3865552 3865552 single base substitution T A intron_variant PRAD-CA 16 3865894 3865894 single base substitution T C intron_variant PRAD-CA 16 3886488 3886488 single base substitution G A intron_variant PRAD-CA 16 3908681 3908681 single base substitution T C intron_variant PRAD-UK 16 3781641 3781641 single base substitution C A downstream_gene_variant PRAD-UK 16 3781641 3781641 single base substitution C A intron_variant PRAD-UK 16 3804620 3804620 single base substitution T C intron_variant PRAD-UK 16 3804620 3804620 single base substitution T C upstream_gene_variant PRAD-UK 16 3805817 3805817 single base substitution C T intron_variant PRAD-UK 16 3805817 3805817 single base substitution C T upstream_gene_variant PRAD-UK 16 3817954 3817954 single base substitution T C intron_variant PRAD-UK 16 3817954 3817954 single base substitution T C upstream_gene_variant PRAD-UK 16 3835233 3835233 single base substitution C G intron_variant PRAD-UK 16 3835233 3835233 single base substitution C G upstream_gene_variant PRAD-UK 16 3841571 3841571 single base substitution C A intron_variant PRAD-UK 16 3860799 3860799 single base substitution A C intron_variant PRAD-UK 16 3867455 3867455 single base substitution C G intron_variant PRAD-UK 16 3908048 3908048 single base substitution C A intron_variant PRAD-UK 16 3908872 3908872 single base substitution A C intron_variant PRAD-UK 16 3912517 3912517 single base substitution T C intron_variant PRAD-UK 16 3912581 3912581 single base substitution G A intron_variant PRAD-UK 16 3918242 3918242 single base substitution T C intron_variant PRAD-US 16 3778253 3778253 single base substitution C T downstream_gene_variant PRAD-US 16 3778253 3778253 single base substitution C T synonymous_variant A2227A 6681G>A PRAD-US 16 3778253 3778253 single base substitution C T synonymous_variant A2265A 6795G>A PRAD-US 16 3778439 3778451 deletion of <=200bp TTGCTGCTGCTGC - downstream_gene_variant PRAD-US 16 3778439 3778451 deletion of <=200bp TTGCTGCTGCTGC - frameshift_variant QQQQQ2161 PRAD-US 16 3778439 3778451 deletion of <=200bp TTGCTGCTGCTGC - frameshift_variant QQQQQ2199 PRAD-US 16 3778738 3778738 single base substitution G A downstream_gene_variant PRAD-US 16 3778738 3778738 single base substitution G A missense_variant R2066C 6196C>T PRAD-US 16 3778738 3778738 single base substitution G A missense_variant R2104C 6310C>T PRAD-US 16 3781218 3781218 single base substitution G A downstream_gene_variant PRAD-US 16 3781218 3781218 single base substitution G A missense_variant T1678M 5033C>T PRAD-US 16 3781218 3781218 single base substitution G A missense_variant T1716M 5147C>T PRAD-US 16 3786756 3786756 single base substitution A G downstream_gene_variant PRAD-US 16 3786756 3786756 single base substitution A G exon_variant PRAD-US 16 3786756 3786756 single base substitution A G synonymous_variant H1447H 4341T>C PRAD-US 16 3786756 3786756 single base substitution A G synonymous_variant H1485H 4455T>C READ-US 16 3799632 3799632 single base substitution C T missense_variant E1240K 3718G>A READ-US 16 3799632 3799632 single base substitution C T missense_variant E1278K 3832G>A READ-US 16 3799632 3799632 single base substitution C T missense_variant E151K 451G>A READ-US 16 3799632 3799632 single base substitution C T missense_variant E46K 136G>A READ-US 16 3799632 3799632 single base substitution C T upstream_gene_variant READ-US 16 3801731 3801731 single base substitution G A intron_variant READ-US 16 3801731 3801731 single base substitution G A stop_gained Q1221* 3661C>T READ-US 16 3801731 3801731 single base substitution G A stop_gained Q1259* 3775C>T READ-US 16 3801731 3801731 single base substitution G A stop_gained Q27* 79C>T READ-US 16 3828135 3828135 single base substitution C A stop_gained E101* 301G>T READ-US 16 3828135 3828135 single base substitution C A stop_gained E13* 37G>T READ-US 16 3828135 3828135 single base substitution C A stop_gained E626* 1876G>T READ-US 16 3828135 3828135 single base substitution C A stop_gained E664* 1990G>T READ-US 16 3828135 3828135 single base substitution C A upstream_gene_variant READ-US 16 3860669 3860669 single base substitution C T missense_variant V304I 910G>A READ-US 16 3900884 3900884 single base substitution G A missense_variant S71L 212C>T RECA-EU 16 3773549 3773549 single base substitution A T downstream_gene_variant RECA-EU 16 3785852 3785852 single base substitution T A downstream_gene_variant RECA-EU 16 3785852 3785852 single base substitution T A intron_variant RECA-EU 16 3788917 3788917 single base substitution T A downstream_gene_variant RECA-EU 16 3788917 3788917 single base substitution T A intron_variant RECA-EU 16 3788917 3788917 single base substitution T A upstream_gene_variant RECA-EU 16 3790545 3790545 single base substitution G C exon_variant RECA-EU 16 3790545 3790545 single base substitution G C missense_variant Q1292E 3874C>G RECA-EU 16 3790545 3790545 single base substitution G C missense_variant Q1330E 3988C>G RECA-EU 16 3790545 3790545 single base substitution G C missense_variant Q203E 607C>G RECA-EU 16 3790545 3790545 single base substitution G C missense_variant Q98E 292C>G RECA-EU 16 3790545 3790545 single base substitution G C upstream_gene_variant RECA-EU 16 3815456 3815456 single base substitution A C downstream_gene_variant RECA-EU 16 3815456 3815456 single base substitution A C intron_variant RECA-EU 16 3818584 3818584 single base substitution G A intron_variant RECA-EU 16 3818584 3818584 single base substitution G A upstream_gene_variant RECA-EU 16 3829456 3829456 single base substitution G T intron_variant RECA-EU 16 3829456 3829456 single base substitution G T upstream_gene_variant RECA-EU 16 3841175 3841175 single base substitution C T intron_variant RECA-EU 16 3847924 3847924 single base substitution A T intron_variant RECA-EU 16 3851340 3851340 single base substitution G A intron_variant RECA-EU 16 3853936 3853936 single base substitution T C intron_variant RECA-EU 16 3857170 3857170 single base substitution C T intron_variant RECA-EU 16 3873782 3873782 single base substitution A G intron_variant RECA-EU 16 3882749 3882749 single base substitution A G intron_variant RECA-EU 16 3885085 3885085 single base substitution G A intron_variant RECA-EU 16 3886265 3886265 single base substitution T A intron_variant RECA-EU 16 3890083 3890083 single base substitution T C intron_variant RECA-EU 16 3904543 3904543 single base substitution T C intron_variant RECA-EU 16 3906224 3906224 single base substitution T C intron_variant RECA-EU 16 3913803 3913803 single base substitution G A intron_variant RECA-EU 16 3916363 3916363 single base substitution G T intron_variant RECA-EU 16 3917900 3917900 single base substitution C T intron_variant RECA-EU 16 3927209 3927209 single base substitution A G intron_variant SKCA-BR 16 3776246 3776246 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 3776246 3776246 single base substitution G A downstream_gene_variant SKCA-BR 16 3776994 3776994 single base substitution A C 3_prime_UTR_variant SKCA-BR 16 3776994 3776994 single base substitution A C downstream_gene_variant SKCA-BR 16 3779210 3779210 single base substitution T G downstream_gene_variant SKCA-BR 16 3779210 3779210 single base substitution T G synonymous_variant P1908P 5724A>C SKCA-BR 16 3779210 3779210 single base substitution T G synonymous_variant P1946P 5838A>C SKCA-BR 16 3780076 3780093 deletion of <=200bp GATGGGATCATGGACAAC - downstream_gene_variant SKCA-BR 16 3780076 3780093 deletion of <=200bp GATGGGATCATGGACAAC - intron_variant SKCA-BR 16 3780429 3780429 single base substitution G A downstream_gene_variant SKCA-BR 16 3780429 3780429 single base substitution G A intron_variant SKCA-BR 16 3781678 3781678 single base substitution T C downstream_gene_variant SKCA-BR 16 3781678 3781678 single base substitution T C intron_variant SKCA-BR 16 3782899 3782899 single base substitution C G downstream_gene_variant SKCA-BR 16 3782899 3782899 single base substitution C G intron_variant SKCA-BR 16 3783087 3783087 single base substitution G A downstream_gene_variant SKCA-BR 16 3783087 3783087 single base substitution G A intron_variant SKCA-BR 16 3785548 3785548 single base substitution C T downstream_gene_variant SKCA-BR 16 3785548 3785548 single base substitution C T intron_variant SKCA-BR 16 3788891 3788891 single base substitution G A downstream_gene_variant SKCA-BR 16 3788891 3788891 single base substitution G A intron_variant SKCA-BR 16 3788891 3788891 single base substitution G A upstream_gene_variant SKCA-BR 16 3789537 3789537 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 3789537 3789537 single base substitution G A downstream_gene_variant SKCA-BR 16 3789537 3789537 single base substitution G A intron_variant SKCA-BR 16 3789537 3789537 single base substitution G A upstream_gene_variant SKCA-BR 16 3790683 3790683 single base substitution G A exon_variant SKCA-BR 16 3790683 3790683 single base substitution G A intron_variant SKCA-BR 16 3790683 3790683 single base substitution G A upstream_gene_variant SKCA-BR 16 3795260 3795260 single base substitution C T intron_variant SKCA-BR 16 3795260 3795260 single base substitution C T upstream_gene_variant SKCA-BR 16 3796028 3796028 single base substitution A C intron_variant SKCA-BR 16 3796028 3796028 single base substitution A C upstream_gene_variant SKCA-BR 16 3797739 3797739 single base substitution G A intron_variant SKCA-BR 16 3797739 3797739 single base substitution G A upstream_gene_variant SKCA-BR 16 3801124 3801124 single base substitution A G intron_variant SKCA-BR 16 3801997 3801997 single base substitution G A intron_variant SKCA-BR 16 3801997 3801997 single base substitution G A upstream_gene_variant SKCA-BR 16 3808215 3808215 single base substitution C T intron_variant SKCA-BR 16 3809418 3809418 single base substitution C T intron_variant SKCA-BR 16 3809731 3809731 single base substitution A G intron_variant SKCA-BR 16 3810351 3810351 single base substitution C T intron_variant SKCA-BR 16 3812362 3812362 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 16 3812362 3812362 insertion of <=200bp - CT intron_variant SKCA-BR 16 3816254 3816254 single base substitution C T downstream_gene_variant SKCA-BR 16 3816254 3816254 single base substitution C T intron_variant SKCA-BR 16 3817048 3817048 single base substitution T C downstream_gene_variant SKCA-BR 16 3817048 3817048 single base substitution T C intron_variant SKCA-BR 16 3818141 3818141 single base substitution T G intron_variant SKCA-BR 16 3818141 3818141 single base substitution T G upstream_gene_variant SKCA-BR 16 3818585 3818585 single base substitution T G intron_variant SKCA-BR 16 3818585 3818585 single base substitution T G upstream_gene_variant SKCA-BR 16 3818615 3818615 single base substitution A G intron_variant SKCA-BR 16 3818615 3818615 single base substitution A G upstream_gene_variant SKCA-BR 16 3821401 3821401 single base substitution G A downstream_gene_variant SKCA-BR 16 3821401 3821401 single base substitution G A intron_variant SKCA-BR 16 3821401 3821401 single base substitution G A upstream_gene_variant SKCA-BR 16 3822216 3822216 single base substitution A T downstream_gene_variant SKCA-BR 16 3822216 3822216 single base substitution A T intron_variant SKCA-BR 16 3822216 3822216 single base substitution A T upstream_gene_variant SKCA-BR 16 3822944 3822944 single base substitution C T downstream_gene_variant SKCA-BR 16 3822944 3822944 single base substitution C T intron_variant SKCA-BR 16 3822944 3822944 single base substitution C T upstream_gene_variant SKCA-BR 16 3825909 3825909 single base substitution C T intron_variant SKCA-BR 16 3825909 3825909 single base substitution C T upstream_gene_variant SKCA-BR 16 3827581 3827581 single base substitution C A intron_variant SKCA-BR 16 3827581 3827581 single base substitution C A upstream_gene_variant SKCA-BR 16 3828345 3828345 single base substitution C T intron_variant SKCA-BR 16 3828345 3828345 single base substitution C T upstream_gene_variant SKCA-BR 16 3835692 3835692 single base substitution G A intron_variant SKCA-BR 16 3835692 3835692 single base substitution G A upstream_gene_variant SKCA-BR 16 3841311 3841311 single base substitution G A intron_variant SKCA-BR 16 3849676 3849676 single base substitution G A intron_variant SKCA-BR 16 3849756 3849756 single base substitution C T intron_variant SKCA-BR 16 3856850 3856850 single base substitution C T intron_variant SKCA-BR 16 3867580 3867580 single base substitution C A intron_variant SKCA-BR 16 3870442 3870442 single base substitution G A intron_variant SKCA-BR 16 3871151 3871151 single base substitution A C intron_variant SKCA-BR 16 3871805 3871805 single base substitution T G intron_variant SKCA-BR 16 3871827 3871827 single base substitution T G intron_variant SKCA-BR 16 3873555 3873555 single base substitution C T intron_variant SKCA-BR 16 3875997 3875997 single base substitution T G intron_variant SKCA-BR 16 3881100 3881100 single base substitution A G intron_variant SKCA-BR 16 3883224 3883224 single base substitution A G intron_variant SKCA-BR 16 3886738 3886738 single base substitution G A intron_variant SKCA-BR 16 3889722 3889722 single base substitution A G intron_variant SKCA-BR 16 3890488 3890488 single base substitution C T intron_variant SKCA-BR 16 3897360 3897360 single base substitution C T intron_variant SKCA-BR 16 3897491 3897491 single base substitution G A intron_variant SKCA-BR 16 3901001 3901001 single base substitution G A missense_variant S32L 95C>T SKCA-BR 16 3902154 3902160 deletion of <=200bp ATTTGTT - intron_variant SKCA-BR 16 3903926 3903926 single base substitution G A intron_variant SKCA-BR 16 3906289 3906289 single base substitution T C intron_variant SKCA-BR 16 3914126 3914126 single base substitution T C intron_variant SKCA-BR 16 3915059 3915059 insertion of <=200bp - CA intron_variant SKCA-BR 16 3918183 3918183 single base substitution C T intron_variant SKCA-BR 16 3921198 3921198 single base substitution A T intron_variant SKCA-BR 16 3927932 3927932 single base substitution G A intron_variant SKCA-BR 16 3930770 3930770 single base substitution T G upstream_gene_variant SKCA-BR 16 3932064 3932064 single base substitution C T upstream_gene_variant SKCA-BR 16 3932326 3932326 single base substitution T A upstream_gene_variant SKCM-US 16 3777725 3777725 single base substitution G A downstream_gene_variant SKCM-US 16 3777725 3777725 single base substitution G A synonymous_variant G2403G 7209C>T SKCM-US 16 3777725 3777725 single base substitution G A synonymous_variant G2441G 7323C>T SKCM-US 16 3777767 3777767 single base substitution G A downstream_gene_variant SKCM-US 16 3777767 3777767 single base substitution G A synonymous_variant V2389V 7167C>T SKCM-US 16 3777767 3777767 single base substitution G A synonymous_variant V2427V 7281C>T SKCM-US 16 3777936 3777936 single base substitution G A downstream_gene_variant SKCM-US 16 3777936 3777936 single base substitution G A missense_variant P2333L 6998C>T SKCM-US 16 3777936 3777936 single base substitution G A missense_variant P2371L 7112C>T SKCM-US 16 3777962 3777962 single base substitution G A downstream_gene_variant SKCM-US 16 3777962 3777962 single base substitution G A synonymous_variant S2324S 6972C>T SKCM-US 16 3777962 3777962 single base substitution G A synonymous_variant S2362S 7086C>T SKCM-US 16 3777981 3777981 single base substitution G A downstream_gene_variant SKCM-US 16 3777981 3777981 single base substitution G A missense_variant S2318F 6953C>T SKCM-US 16 3777981 3777981 single base substitution G A missense_variant S2356F 7067C>T SKCM-US 16 3778043 3778043 single base substitution G A downstream_gene_variant SKCM-US 16 3778043 3778043 single base substitution G A synonymous_variant I2297I 6891C>T SKCM-US 16 3778043 3778043 single base substitution G A synonymous_variant I2335I 7005C>T SKCM-US 16 3778303 3778305 deletion of <=200bp GCT - disruptive_inframe_deletion QR2210R SKCM-US 16 3778303 3778305 deletion of <=200bp GCT - disruptive_inframe_deletion QR2248R SKCM-US 16 3778303 3778305 deletion of <=200bp GCT - downstream_gene_variant SKCM-US 16 3778737 3778737 single base substitution C G downstream_gene_variant SKCM-US 16 3778737 3778737 single base substitution C G missense_variant R2066P 6197G>C SKCM-US 16 3778737 3778737 single base substitution C G missense_variant R2104P 6311G>C SKCM-US 16 3778993 3778993 single base substitution C A downstream_gene_variant SKCM-US 16 3778993 3778993 single base substitution C A missense_variant G1981W 5941G>T SKCM-US 16 3778993 3778993 single base substitution C A missense_variant G2019W 6055G>T SKCM-US 16 3779649 3779649 single base substitution C T downstream_gene_variant SKCM-US 16 3779649 3779649 single base substitution C T missense_variant R1762Q 5285G>A SKCM-US 16 3779649 3779649 single base substitution C T missense_variant R1800Q 5399G>A SKCM-US 16 3779715 3779715 single base substitution G A downstream_gene_variant SKCM-US 16 3779715 3779715 single base substitution G A missense_variant S1740L 5219C>T SKCM-US 16 3779715 3779715 single base substitution G A missense_variant S1778L 5333C>T SKCM-US 16 3786113 3786113 single base substitution T C downstream_gene_variant SKCM-US 16 3786113 3786113 single base substitution T C exon_variant SKCM-US 16 3786113 3786113 single base substitution T C missense_variant E1513G 4538A>G SKCM-US 16 3786113 3786113 single base substitution T C missense_variant E1551G 4652A>G SKCM-US 16 3786779 3786779 single base substitution C T downstream_gene_variant SKCM-US 16 3786779 3786779 single base substitution C T exon_variant SKCM-US 16 3786779 3786779 single base substitution C T missense_variant E1440K 4318G>A SKCM-US 16 3786779 3786779 single base substitution C T missense_variant E1478K 4432G>A SKCM-US 16 3788618 3788618 single base substitution G A downstream_gene_variant SKCM-US 16 3788618 3788618 single base substitution G A intron_variant SKCM-US 16 3788618 3788618 single base substitution G A missense_variant R1408C 4222C>T SKCM-US 16 3788618 3788618 single base substitution G A missense_variant R1446C 4336C>T SKCM-US 16 3788618 3788618 single base substitution G A upstream_gene_variant SKCM-US 16 3790455 3790455 single base substitution G A exon_variant SKCM-US 16 3790455 3790455 single base substitution G A stop_gained R128* 382C>T SKCM-US 16 3790455 3790455 single base substitution G A stop_gained R1322* 3964C>T SKCM-US 16 3790455 3790455 single base substitution G A stop_gained R1360* 4078C>T SKCM-US 16 3790455 3790455 single base substitution G A stop_gained R233* 697C>T SKCM-US 16 3790455 3790455 single base substitution G A upstream_gene_variant SKCM-US 16 3794898 3794898 single base substitution T A exon_variant SKCM-US 16 3794898 3794898 single base substitution T A stop_gained K1289* 3865A>T SKCM-US 16 3794898 3794898 single base substitution T A stop_gained K1327* 3979A>T SKCM-US 16 3794898 3794898 single base substitution T A stop_gained K200* 598A>T SKCM-US 16 3794898 3794898 single base substitution T A stop_gained K95* 283A>T SKCM-US 16 3794898 3794898 single base substitution T A upstream_gene_variant SKCM-US 16 3795308 3795308 single base substitution A G exon_variant SKCM-US 16 3795308 3795308 single base substitution A G missense_variant V1257A 3770T>C SKCM-US 16 3795308 3795308 single base substitution A G missense_variant V1295A 3884T>C SKCM-US 16 3795308 3795308 single base substitution A G missense_variant V168A 503T>C SKCM-US 16 3795308 3795308 single base substitution A G missense_variant V63A 188T>C SKCM-US 16 3795308 3795308 single base substitution A G upstream_gene_variant SKCM-US 16 3795352 3795352 single base substitution G A exon_variant SKCM-US 16 3795352 3795352 single base substitution G A synonymous_variant F1242F 3726C>T SKCM-US 16 3795352 3795352 single base substitution G A synonymous_variant F1280F 3840C>T SKCM-US 16 3795352 3795352 single base substitution G A synonymous_variant F153F 459C>T SKCM-US 16 3795352 3795352 single base substitution G A synonymous_variant F48F 144C>T SKCM-US 16 3795352 3795352 single base substitution G A upstream_gene_variant SKCM-US 16 3808895 3808895 single base substitution G C missense_variant P1072R 3215C>G SKCM-US 16 3808895 3808895 single base substitution G C missense_variant P1110R 3329C>G SKCM-US 16 3808895 3808895 single base substitution G C missense_variant P64R 191C>G SKCM-US 16 3817765 3817765 single base substitution C T exon_variant SKCM-US 16 3817765 3817765 single base substitution C T missense_variant G1031D 3092G>A SKCM-US 16 3817765 3817765 single base substitution C T missense_variant G1069D 3206G>A SKCM-US 16 3817765 3817765 single base substitution C T missense_variant G23D 68G>A SKCM-US 16 3819257 3819257 single base substitution G T downstream_gene_variant SKCM-US 16 3819257 3819257 single base substitution G T exon_variant SKCM-US 16 3819257 3819257 single base substitution G T missense_variant P955H 2864C>A SKCM-US 16 3819257 3819257 single base substitution G T missense_variant P993H 2978C>A SKCM-US 16 3819257 3819257 single base substitution G T upstream_gene_variant SKCM-US 16 3819272 3819272 single base substitution G A downstream_gene_variant SKCM-US 16 3819272 3819272 single base substitution G A exon_variant SKCM-US 16 3819272 3819272 single base substitution G A missense_variant P950L 2849C>T SKCM-US 16 3819272 3819272 single base substitution G A missense_variant P988L 2963C>T SKCM-US 16 3819272 3819272 single base substitution G A upstream_gene_variant SKCM-US 16 3820669 3820669 single base substitution G A downstream_gene_variant SKCM-US 16 3820669 3820669 single base substitution G A exon_variant SKCM-US 16 3820669 3820669 single base substitution G A missense_variant P890S 2668C>T SKCM-US 16 3820669 3820669 single base substitution G A missense_variant P928S 2782C>T SKCM-US 16 3820669 3820669 single base substitution G A upstream_gene_variant SKCM-US 16 3824617 3824617 single base substitution G A exon_variant SKCM-US 16 3824617 3824617 single base substitution G A missense_variant P168S 502C>T SKCM-US 16 3824617 3824617 single base substitution G A missense_variant P708S 2122C>T SKCM-US 16 3824617 3824617 single base substitution G A missense_variant P746S 2236C>T SKCM-US 16 3824617 3824617 single base substitution G A missense_variant P95S 283C>T SKCM-US 16 3824617 3824617 single base substitution G A upstream_gene_variant SKCM-US 16 3827650 3827650 single base substitution G A intron_variant SKCM-US 16 3827650 3827650 single base substitution G A synonymous_variant L57L 169C>T SKCM-US 16 3827650 3827650 single base substitution G A synonymous_variant L670L 2008C>T SKCM-US 16 3827650 3827650 single base substitution G A synonymous_variant L708L 2122C>T SKCM-US 16 3827650 3827650 single base substitution G A upstream_gene_variant SKCM-US 16 3828061 3828061 single base substitution C T synonymous_variant P125P 375G>A SKCM-US 16 3828061 3828061 single base substitution C T synonymous_variant P37P 111G>A SKCM-US 16 3828061 3828061 single base substitution C T synonymous_variant P650P 1950G>A SKCM-US 16 3828061 3828061 single base substitution C T synonymous_variant P688P 2064G>A SKCM-US 16 3828061 3828061 single base substitution C T upstream_gene_variant SKCM-US 16 3828796 3828796 single base substitution G A missense_variant P53S 157C>T SKCM-US 16 3828796 3828796 single base substitution G A missense_variant P578S 1732C>T SKCM-US 16 3828796 3828796 single base substitution G A missense_variant P616S 1846C>T SKCM-US 16 3828796 3828796 single base substitution G A upstream_gene_variant SKCM-US 16 3832835 3832835 single base substitution G A missense_variant P437S 1309C>T SKCM-US 16 3832835 3832835 single base substitution G A missense_variant P475S 1423C>T SKCM-US 16 3832835 3832835 single base substitution G A upstream_gene_variant SKCM-US 16 3842066 3842066 single base substitution T C intron_variant SKCM-US 16 3842066 3842066 single base substitution T C missense_variant I416V 1246A>G SKCM-US 16 3843402 3843402 single base substitution C A missense_variant G401W 1201G>T SKCM-US 16 3860727 3860727 single base substitution T A synonymous_variant G284G 852A>T SKCM-US 16 3900298 3900298 single base substitution C T splice_region_variant SKCM-US 16 3900527 3900527 single base substitution T A missense_variant N190I 569A>T SKCM-US 16 3900705 3900705 single base substitution G A missense_variant P131S 391C>T SKCM-US 16 3900838 3900838 single base substitution T A synonymous_variant I86I 258A>T STAD-US 16 3777763 3777763 single base substitution C T downstream_gene_variant STAD-US 16 3777763 3777763 single base substitution C T missense_variant D2391N 7171G>A STAD-US 16 3777763 3777763 single base substitution C T missense_variant D2429N 7285G>A STAD-US 16 3777887 3777887 single base substitution G A downstream_gene_variant STAD-US 16 3777887 3777887 single base substitution G A synonymous_variant L2349L 7047C>T STAD-US 16 3777887 3777887 single base substitution G A synonymous_variant L2387L 7161C>T STAD-US 16 3777898 3777898 deletion of <=200bp G - downstream_gene_variant STAD-US 16 3777898 3777898 deletion of <=200bp G - frameshift_variant H2346 STAD-US 16 3777898 3777898 deletion of <=200bp G - frameshift_variant H2384 STAD-US 16 3778018 3778018 single base substitution G A downstream_gene_variant STAD-US 16 3778018 3778018 single base substitution G A missense_variant R2306W 6916C>T STAD-US 16 3778018 3778018 single base substitution G A missense_variant R2344W 7030C>T STAD-US 16 3778282 3778282 deletion of <=200bp G - downstream_gene_variant STAD-US 16 3778282 3778282 deletion of <=200bp G - frameshift_variant L2218 STAD-US 16 3778282 3778282 deletion of <=200bp G - frameshift_variant L2256 STAD-US 16 3778387 3778387 single base substitution T C downstream_gene_variant STAD-US 16 3778387 3778387 single base substitution T C missense_variant M2183V 6547A>G STAD-US 16 3778387 3778387 single base substitution T C missense_variant M2221V 6661A>G STAD-US 16 3778427 3778427 single base substitution T C downstream_gene_variant STAD-US 16 3778427 3778427 single base substitution T C synonymous_variant Q2169Q 6507A>G STAD-US 16 3778427 3778427 single base substitution T C synonymous_variant Q2207Q 6621A>G STAD-US 16 3778452 3778452 single base substitution T A downstream_gene_variant STAD-US 16 3778452 3778452 single base substitution T A missense_variant Q2161L 6482A>T STAD-US 16 3778452 3778452 single base substitution T A missense_variant Q2199L 6596A>T STAD-US 16 3778617 3778617 single base substitution G A downstream_gene_variant STAD-US 16 3778617 3778617 single base substitution G A missense_variant A2106V 6317C>T STAD-US 16 3778617 3778617 single base substitution G A missense_variant A2144V 6431C>T STAD-US 16 3778706 3778706 single base substitution G A downstream_gene_variant STAD-US 16 3778706 3778706 single base substitution G A synonymous_variant G2076G 6228C>T STAD-US 16 3778706 3778706 single base substitution G A synonymous_variant G2114G 6342C>T STAD-US 16 3778795 3778795 single base substitution G A downstream_gene_variant STAD-US 16 3778795 3778795 single base substitution G A stop_gained Q2047* 6139C>T STAD-US 16 3778795 3778795 single base substitution G A stop_gained Q2085* 6253C>T STAD-US 16 3778834 3778834 single base substitution G A downstream_gene_variant STAD-US 16 3778834 3778834 single base substitution G A missense_variant R2034W 6100C>T STAD-US 16 3778834 3778834 single base substitution G A missense_variant R2072W 6214C>T STAD-US 16 3779597 3779597 single base substitution C T downstream_gene_variant STAD-US 16 3779597 3779597 single base substitution C T synonymous_variant P1779P 5337G>A STAD-US 16 3779597 3779597 single base substitution C T synonymous_variant P1817P 5451G>A STAD-US 16 3779644 3779644 single base substitution C T downstream_gene_variant STAD-US 16 3779644 3779644 single base substitution C T missense_variant V1764M 5290G>A STAD-US 16 3779644 3779644 single base substitution C T missense_variant V1802M 5404G>A STAD-US 16 3781199 3781199 single base substitution C T downstream_gene_variant STAD-US 16 3781199 3781199 single base substitution C T synonymous_variant V1684V 5052G>A STAD-US 16 3781199 3781199 single base substitution C T synonymous_variant V1722V 5166G>A STAD-US 16 3781302 3781302 single base substitution G A downstream_gene_variant STAD-US 16 3781302 3781302 single base substitution G A missense_variant T1650M 4949C>T STAD-US 16 3781302 3781302 single base substitution G A missense_variant T1688M 5063C>T STAD-US 16 3781373 3781373 single base substitution G A downstream_gene_variant STAD-US 16 3781373 3781373 single base substitution G A synonymous_variant R1626R 4878C>T STAD-US 16 3781373 3781373 single base substitution G A synonymous_variant R1664R 4992C>T STAD-US 16 3781384 3781384 single base substitution T C downstream_gene_variant STAD-US 16 3781384 3781384 single base substitution T C missense_variant M1623V 4867A>G STAD-US 16 3781384 3781384 single base substitution T C missense_variant M1661V 4981A>G STAD-US 16 3781417 3781417 single base substitution C T downstream_gene_variant STAD-US 16 3781417 3781417 single base substitution C T missense_variant V1612I 4834G>A STAD-US 16 3781417 3781417 single base substitution C T missense_variant V1650I 4948G>A STAD-US 16 3781465 3781465 single base substitution C T downstream_gene_variant STAD-US 16 3781465 3781465 single base substitution C T missense_variant V1596M 4786G>A STAD-US 16 3781465 3781465 single base substitution C T missense_variant V1634M 4900G>A STAD-US 16 3781793 3781793 single base substitution A G downstream_gene_variant STAD-US 16 3781793 3781793 single base substitution A G missense_variant M1587T 4760T>C STAD-US 16 3781793 3781793 single base substitution A G missense_variant M1625T 4874T>C STAD-US 16 3781863 3781863 single base substitution G A downstream_gene_variant STAD-US 16 3781863 3781863 single base substitution G A missense_variant R1564C 4690C>T STAD-US 16 3781863 3781863 single base substitution G A missense_variant R1602C 4804C>T STAD-US 16 3781927 3781927 single base substitution G A downstream_gene_variant STAD-US 16 3781927 3781927 single base substitution G A exon_variant STAD-US 16 3781927 3781927 single base substitution G A synonymous_variant G1542G 4626C>T STAD-US 16 3781927 3781927 single base substitution G A synonymous_variant G1580G 4740C>T STAD-US 16 3786141 3786141 single base substitution C T downstream_gene_variant STAD-US 16 3786141 3786141 single base substitution C T exon_variant STAD-US 16 3786141 3786141 single base substitution C T missense_variant G1504S 4510G>A STAD-US 16 3786141 3786141 single base substitution C T missense_variant G1542S 4624G>A STAD-US 16 3786655 3786655 single base substitution T C downstream_gene_variant STAD-US 16 3786655 3786655 single base substitution T C exon_variant STAD-US 16 3786655 3786655 single base substitution T C missense_variant Y1481C 4442A>G STAD-US 16 3786655 3786655 single base substitution T C missense_variant Y1519C 4556A>G STAD-US 16 3786719 3786719 single base substitution G A downstream_gene_variant STAD-US 16 3786719 3786719 single base substitution G A exon_variant STAD-US 16 3786719 3786719 single base substitution G A stop_gained R1460* 4378C>T STAD-US 16 3786719 3786719 single base substitution G A stop_gained R1498* 4492C>T STAD-US 16 3786799 3786799 single base substitution A T downstream_gene_variant STAD-US 16 3786799 3786799 single base substitution A T exon_variant STAD-US 16 3786799 3786799 single base substitution A T missense_variant I1433N 4298T>A STAD-US 16 3786799 3786799 single base substitution A T missense_variant I1471N 4412T>A STAD-US 16 3788617 3788617 single base substitution C T downstream_gene_variant STAD-US 16 3788617 3788617 single base substitution C T intron_variant STAD-US 16 3788617 3788617 single base substitution C T missense_variant R1408H 4223G>A STAD-US 16 3788617 3788617 single base substitution C T missense_variant R1446H 4337G>A STAD-US 16 3788617 3788617 single base substitution C T upstream_gene_variant STAD-US 16 3789629 3789629 deletion of <=200bp A - downstream_gene_variant STAD-US 16 3789629 3789629 deletion of <=200bp A - exon_variant STAD-US 16 3789629 3789629 deletion of <=200bp A - frameshift_variant F1372 STAD-US 16 3789629 3789629 deletion of <=200bp A - frameshift_variant F1410 STAD-US 16 3789629 3789629 deletion of <=200bp A - frameshift_variant F178 STAD-US 16 3789629 3789629 deletion of <=200bp A - frameshift_variant F283 STAD-US 16 3789629 3789629 deletion of <=200bp A - intron_variant STAD-US 16 3789629 3789629 deletion of <=200bp A - upstream_gene_variant STAD-US 16 3789647 3789647 single base substitution G A downstream_gene_variant STAD-US 16 3789647 3789647 single base substitution G A exon_variant STAD-US 16 3789647 3789647 single base substitution G A intron_variant STAD-US 16 3789647 3789647 single base substitution G A synonymous_variant G1366G 4098C>T STAD-US 16 3789647 3789647 single base substitution G A synonymous_variant G1404G 4212C>T STAD-US 16 3789647 3789647 single base substitution G A synonymous_variant G172G 516C>T STAD-US 16 3789647 3789647 single base substitution G A synonymous_variant G277G 831C>T STAD-US 16 3789647 3789647 single base substitution G A upstream_gene_variant STAD-US 16 3790455 3790455 single base substitution G A exon_variant STAD-US 16 3790455 3790455 single base substitution G A stop_gained R128* 382C>T STAD-US 16 3790455 3790455 single base substitution G A stop_gained R1322* 3964C>T STAD-US 16 3790455 3790455 single base substitution G A stop_gained R1360* 4078C>T STAD-US 16 3790455 3790455 single base substitution G A stop_gained R233* 697C>T STAD-US 16 3790455 3790455 single base substitution G A upstream_gene_variant STAD-US 16 3795299 3795299 single base substitution T C exon_variant STAD-US 16 3795299 3795299 single base substitution T C missense_variant Y1260C 3779A>G STAD-US 16 3795299 3795299 single base substitution T C missense_variant Y1298C 3893A>G STAD-US 16 3795299 3795299 single base substitution T C missense_variant Y171C 512A>G STAD-US 16 3795299 3795299 single base substitution T C missense_variant Y66C 197A>G STAD-US 16 3795299 3795299 single base substitution T C upstream_gene_variant STAD-US 16 3799628 3799628 single base substitution G A missense_variant P1241L 3722C>T STAD-US 16 3799628 3799628 single base substitution G A missense_variant P1279L 3836C>T STAD-US 16 3799628 3799628 single base substitution G A missense_variant P152L 455C>T STAD-US 16 3799628 3799628 single base substitution G A missense_variant P47L 140C>T STAD-US 16 3799628 3799628 single base substitution G A upstream_gene_variant STAD-US 16 3807913 3807913 single base substitution C T missense_variant R1131H 3392G>A STAD-US 16 3807913 3807913 single base substitution C T missense_variant R1169H 3506G>A STAD-US 16 3807913 3807913 single base substitution C T missense_variant R123H 368G>A STAD-US 16 3808004 3808004 single base substitution T C missense_variant K1101E 3301A>G STAD-US 16 3808004 3808004 single base substitution T C missense_variant K1139E 3415A>G STAD-US 16 3808004 3808004 single base substitution T C missense_variant K93E 277A>G STAD-US 16 3808953 3808953 single base substitution G A missense_variant R1053C 3157C>T STAD-US 16 3808953 3808953 single base substitution G A missense_variant R1091C 3271C>T STAD-US 16 3808953 3808953 single base substitution G A missense_variant R45C 133C>T STAD-US 16 3817721 3817721 insertion of <=200bp - T exon_variant STAD-US 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I1046N? STAD-US 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I1084N? STAD-US 16 3817721 3817721 insertion of <=200bp - T frameshift_variant I38N? STAD-US 16 3820608 3820608 single base substitution T C downstream_gene_variant STAD-US 16 3820608 3820608 single base substitution T C exon_variant STAD-US 16 3820608 3820608 single base substitution T C missense_variant Q910R 2729A>G STAD-US 16 3820608 3820608 single base substitution T C missense_variant Q948R 2843A>G STAD-US 16 3820608 3820608 single base substitution T C upstream_gene_variant STAD-US 16 3820836 3820836 single base substitution G A downstream_gene_variant STAD-US 16 3820836 3820836 single base substitution G A missense_variant T834M 2501C>T STAD-US 16 3820836 3820836 single base substitution G A missense_variant T872M 2615C>T STAD-US 16 3820836 3820836 single base substitution G A upstream_gene_variant STAD-US 16 3820945 3820945 single base substitution G T downstream_gene_variant STAD-US 16 3820945 3820945 single base substitution G T missense_variant L798M 2392C>A STAD-US 16 3820945 3820945 single base substitution G T missense_variant L836M 2506C>A STAD-US 16 3820945 3820945 single base substitution G T upstream_gene_variant STAD-US 16 3823777 3823777 single base substitution G A exon_variant STAD-US 16 3823777 3823777 single base substitution G A missense_variant P162L 485C>T STAD-US 16 3823777 3823777 single base substitution G A missense_variant P235L 704C>T STAD-US 16 3823777 3823777 single base substitution G A missense_variant P775L 2324C>T STAD-US 16 3823777 3823777 single base substitution G A missense_variant P813L 2438C>T STAD-US 16 3823777 3823777 single base substitution G A upstream_gene_variant STAD-US 16 3824574 3824574 single base substitution G T exon_variant STAD-US 16 3824574 3824574 single base substitution G T missense_variant P109Q 326C>A STAD-US 16 3824574 3824574 single base substitution G T missense_variant P182Q 545C>A STAD-US 16 3824574 3824574 single base substitution G T missense_variant P722Q 2165C>A STAD-US 16 3824574 3824574 single base substitution G T missense_variant P760Q 2279C>A STAD-US 16 3824574 3824574 single base substitution G T upstream_gene_variant STAD-US 16 3824616 3824616 insertion of <=200bp - G exon_variant STAD-US 16 3824616 3824616 insertion of <=200bp - G frameshift_variant P168P? STAD-US 16 3824616 3824616 insertion of <=200bp - G frameshift_variant P708P? STAD-US 16 3824616 3824616 insertion of <=200bp - G frameshift_variant P746P? STAD-US 16 3824616 3824616 insertion of <=200bp - G frameshift_variant P95P? STAD-US 16 3824616 3824616 insertion of <=200bp - G upstream_gene_variant STAD-US 16 3828749 3828749 single base substitution G T synonymous_variant A593A 1779C>A STAD-US 16 3828749 3828749 single base substitution G T synonymous_variant A631A 1893C>A STAD-US 16 3828749 3828749 single base substitution G T synonymous_variant A68A 204C>A STAD-US 16 3828749 3828749 single base substitution G T upstream_gene_variant STAD-US 16 3828769 3828769 single base substitution G A missense_variant R587C 1759C>T STAD-US 16 3828769 3828769 single base substitution G A missense_variant R625C 1873C>T STAD-US 16 3828769 3828769 single base substitution G A missense_variant R62C 184C>T STAD-US 16 3828769 3828769 single base substitution G A upstream_gene_variant STAD-US 16 3828788 3828788 single base substitution G A synonymous_variant P55P 165C>T STAD-US 16 3828788 3828788 single base substitution G A synonymous_variant P580P 1740C>T STAD-US 16 3828788 3828788 single base substitution G A synonymous_variant P618P 1854C>T STAD-US 16 3828788 3828788 single base substitution G A upstream_gene_variant STAD-US 16 3843416 3843416 single base substitution G A missense_variant T396M 1187C>T STAD-US 16 3843433 3843433 single base substitution G A synonymous_variant N390N 1170C>T STAD-US 16 3900321 3900321 single base substitution C T missense_variant A259T 775G>A STAD-US 16 3900561 3900561 single base substitution C T missense_variant A179T 535G>A THCA-US 16 3828107 3828107 single base substitution A T stop_gained L110* 329T>A THCA-US 16 3828107 3828107 single base substitution A T stop_gained L22* 65T>A THCA-US 16 3828107 3828107 single base substitution A T stop_gained L635* 1904T>A THCA-US 16 3828107 3828107 single base substitution A T stop_gained L673* 2018T>A THCA-US 16 3828107 3828107 single base substitution A T upstream_gene_variant UCEC-US 16 3777856 3777856 single base substitution C A downstream_gene_variant UCEC-US 16 3777856 3777856 single base substitution C A stop_gained G2360* 7078G>T UCEC-US 16 3777856 3777856 single base substitution C A stop_gained G2398* 7192G>T UCEC-US 16 3777959 3777959 single base substitution C T downstream_gene_variant UCEC-US 16 3777959 3777959 single base substitution C T synonymous_variant P2325P 6975G>A UCEC-US 16 3777959 3777959 single base substitution C T synonymous_variant P2363P 7089G>A UCEC-US 16 3778099 3778099 single base substitution G T downstream_gene_variant UCEC-US 16 3778099 3778099 single base substitution G T missense_variant Q2279K 6835C>A UCEC-US 16 3778099 3778099 single base substitution G T missense_variant Q2317K 6949C>A UCEC-US 16 3778177 3778177 single base substitution G T downstream_gene_variant UCEC-US 16 3778177 3778177 single base substitution G T missense_variant L2253M 6757C>A UCEC-US 16 3778177 3778177 single base substitution G T missense_variant L2291M 6871C>A UCEC-US 16 3778607 3778607 single base substitution A C downstream_gene_variant UCEC-US 16 3778607 3778607 single base substitution A C synonymous_variant A2109A 6327T>G UCEC-US 16 3778607 3778607 single base substitution A C synonymous_variant A2147A 6441T>G UCEC-US 16 3778624 3778624 single base substitution G T downstream_gene_variant UCEC-US 16 3778624 3778624 single base substitution G T missense_variant L2104M 6310C>A UCEC-US 16 3778624 3778624 single base substitution G T missense_variant L2142M 6424C>A UCEC-US 16 3778738 3778738 single base substitution G A downstream_gene_variant UCEC-US 16 3778738 3778738 single base substitution G A missense_variant R2066C 6196C>T UCEC-US 16 3778738 3778738 single base substitution G A missense_variant R2104C 6310C>T UCEC-US 16 3778767 3778767 single base substitution G A downstream_gene_variant UCEC-US 16 3778767 3778767 single base substitution G A missense_variant P2056L 6167C>T UCEC-US 16 3778767 3778767 single base substitution G A missense_variant P2094L 6281C>T UCEC-US 16 3779350 3779350 single base substitution G C downstream_gene_variant UCEC-US 16 3779350 3779350 single base substitution G C missense_variant P1862A 5584C>G UCEC-US 16 3779350 3779350 single base substitution G C missense_variant P1900A 5698C>G UCEC-US 16 3779704 3779704 single base substitution C T downstream_gene_variant UCEC-US 16 3779704 3779704 single base substitution C T missense_variant A1744T 5230G>A UCEC-US 16 3779704 3779704 single base substitution C T missense_variant A1782T 5344G>A UCEC-US 16 3781241 3781241 single base substitution G A downstream_gene_variant UCEC-US 16 3781241 3781241 single base substitution G A synonymous_variant N1670N 5010C>T UCEC-US 16 3781241 3781241 single base substitution G A synonymous_variant N1708N 5124C>T UCEC-US 16 3781321 3781321 single base substitution G A downstream_gene_variant UCEC-US 16 3781321 3781321 single base substitution G A missense_variant R1644C 4930C>T UCEC-US 16 3781321 3781321 single base substitution G A missense_variant R1682C 5044C>T UCEC-US 16 3781464 3781464 single base substitution A G downstream_gene_variant UCEC-US 16 3781464 3781464 single base substitution A G missense_variant V1596A 4787T>C UCEC-US 16 3781464 3781464 single base substitution A G missense_variant V1634A 4901T>C UCEC-US 16 3786666 3786666 single base substitution G C downstream_gene_variant UCEC-US 16 3786666 3786666 single base substitution G C exon_variant UCEC-US 16 3786666 3786666 single base substitution G C missense_variant I1477M 4431C>G UCEC-US 16 3786666 3786666 single base substitution G C missense_variant I1515M 4545C>G UCEC-US 16 3786728 3786728 single base substitution T A downstream_gene_variant UCEC-US 16 3786728 3786728 single base substitution T A exon_variant UCEC-US 16 3786728 3786728 single base substitution T A stop_gained K1457* 4369A>T UCEC-US 16 3786728 3786728 single base substitution T A stop_gained K1495* 4483A>T UCEC-US 16 3786792 3786792 deletion of <=200bp G - downstream_gene_variant UCEC-US 16 3786792 3786792 deletion of <=200bp G - exon_variant UCEC-US 16 3786792 3786792 deletion of <=200bp G - frameshift_variant A1435 UCEC-US 16 3786792 3786792 deletion of <=200bp G - frameshift_variant A1473 UCEC-US 16 3788637 3788637 single base substitution G T downstream_gene_variant UCEC-US 16 3788637 3788637 single base substitution G T intron_variant UCEC-US 16 3788637 3788637 single base substitution G T missense_variant F1401L 4203C>A UCEC-US 16 3788637 3788637 single base substitution G T missense_variant F1439L 4317C>A UCEC-US 16 3788637 3788637 single base substitution G T upstream_gene_variant UCEC-US 16 3788643 3788643 single base substitution A C downstream_gene_variant UCEC-US 16 3788643 3788643 single base substitution A C intron_variant UCEC-US 16 3788643 3788643 single base substitution A C missense_variant I1399M 4197T>G UCEC-US 16 3788643 3788643 single base substitution A C missense_variant I1437M 4311T>G UCEC-US 16 3788643 3788643 single base substitution A C upstream_gene_variant UCEC-US 16 3789608 3789608 single base substitution G T downstream_gene_variant UCEC-US 16 3789608 3789608 single base substitution G T exon_variant UCEC-US 16 3789608 3789608 single base substitution G T intron_variant UCEC-US 16 3789608 3789608 single base substitution G T stop_gained Y1379* 4137C>A UCEC-US 16 3789608 3789608 single base substitution G T stop_gained Y1417* 4251C>A UCEC-US 16 3789608 3789608 single base substitution G T stop_gained Y185* 555C>A UCEC-US 16 3789608 3789608 single base substitution G T upstream_gene_variant UCEC-US 16 3789648 3789648 single base substitution C A downstream_gene_variant UCEC-US 16 3789648 3789648 single base substitution C A exon_variant UCEC-US 16 3789648 3789648 single base substitution C A intron_variant UCEC-US 16 3789648 3789648 single base substitution C A missense_variant G1366V 4097G>T UCEC-US 16 3789648 3789648 single base substitution C A missense_variant G1404V 4211G>T UCEC-US 16 3789648 3789648 single base substitution C A missense_variant G172V 515G>T UCEC-US 16 3789648 3789648 single base substitution C A missense_variant G277V 830G>T UCEC-US 16 3789648 3789648 single base substitution C A upstream_gene_variant UCEC-US 16 3790499 3790499 single base substitution A C exon_variant UCEC-US 16 3790499 3790499 single base substitution A C missense_variant F113C 338T>G UCEC-US 16 3790499 3790499 single base substitution A C missense_variant F1307C 3920T>G UCEC-US 16 3790499 3790499 single base substitution A C missense_variant F1345C 4034T>G UCEC-US 16 3790499 3790499 single base substitution A C missense_variant F218C 653T>G UCEC-US 16 3790499 3790499 single base substitution A C upstream_gene_variant UCEC-US 16 3794921 3794921 single base substitution C T exon_variant UCEC-US 16 3794921 3794921 single base substitution C T missense_variant R1281Q 3842G>A UCEC-US 16 3794921 3794921 single base substitution C T missense_variant R1319Q 3956G>A UCEC-US 16 3794921 3794921 single base substitution C T missense_variant R192Q 575G>A UCEC-US 16 3794921 3794921 single base substitution C T missense_variant R87Q 260G>A UCEC-US 16 3794921 3794921 single base substitution C T upstream_gene_variant UCEC-US 16 3801769 3801769 single base substitution C T intron_variant UCEC-US 16 3801769 3801769 single base substitution C T missense_variant G1208D 3623G>A UCEC-US 16 3801769 3801769 single base substitution C T missense_variant G1246D 3737G>A UCEC-US 16 3801769 3801769 single base substitution C T missense_variant G14D 41G>A UCEC-US 16 3807984 3807984 single base substitution C T synonymous_variant G1107G 3321G>A UCEC-US 16 3807984 3807984 single base substitution C T synonymous_variant G1145G 3435G>A UCEC-US 16 3807984 3807984 single base substitution C T synonymous_variant G99G 297G>A UCEC-US 16 3808903 3808903 single base substitution C T synonymous_variant E1069E 3207G>A UCEC-US 16 3808903 3808903 single base substitution C T synonymous_variant E1107E 3321G>A UCEC-US 16 3808903 3808903 single base substitution C T synonymous_variant E61E 183G>A UCEC-US 16 3817857 3817857 single base substitution T C exon_variant UCEC-US 16 3817857 3817857 single base substitution T C missense_variant I1000M 3000A>G UCEC-US 16 3817857 3817857 single base substitution T C missense_variant I1038M 3114A>G UCEC-US 16 3817857 3817857 single base substitution T C upstream_gene_variant UCEC-US 16 3820640 3820640 single base substitution C T downstream_gene_variant UCEC-US 16 3820640 3820640 single base substitution C T exon_variant UCEC-US 16 3820640 3820640 single base substitution C T synonymous_variant P899P 2697G>A UCEC-US 16 3820640 3820640 single base substitution C T synonymous_variant P937P 2811G>A UCEC-US 16 3820640 3820640 single base substitution C T upstream_gene_variant UCEC-US 16 3820743 3820743 single base substitution G T downstream_gene_variant UCEC-US 16 3820743 3820743 single base substitution G T missense_variant P865H 2594C>A UCEC-US 16 3820743 3820743 single base substitution G T missense_variant P903H 2708C>A UCEC-US 16 3820743 3820743 single base substitution G T upstream_gene_variant UCEC-US 16 3820878 3820878 single base substitution G A downstream_gene_variant UCEC-US 16 3820878 3820878 single base substitution G A missense_variant P820L 2459C>T UCEC-US 16 3820878 3820878 single base substitution G A missense_variant P858L 2573C>T UCEC-US 16 3820878 3820878 single base substitution G A upstream_gene_variant UCEC-US 16 3823921 3823921 single base substitution G T exon_variant UCEC-US 16 3823921 3823921 single base substitution G T missense_variant S114Y 341C>A UCEC-US 16 3823921 3823921 single base substitution G T missense_variant S187Y 560C>A UCEC-US 16 3823921 3823921 single base substitution G T missense_variant S727Y 2180C>A UCEC-US 16 3823921 3823921 single base substitution G T missense_variant S765Y 2294C>A UCEC-US 16 3823921 3823921 single base substitution G T upstream_gene_variant UCEC-US 16 3827632 3827632 single base substitution G A intron_variant UCEC-US 16 3827632 3827632 single base substitution G A missense_variant R63C 187C>T UCEC-US 16 3827632 3827632 single base substitution G A missense_variant R676C 2026C>T UCEC-US 16 3827632 3827632 single base substitution G A missense_variant R714C 2140C>T UCEC-US 16 3827632 3827632 single base substitution G A upstream_gene_variant UCEC-US 16 3828110 3828110 single base substitution C T missense_variant R109H 326G>A UCEC-US 16 3828110 3828110 single base substitution C T missense_variant R21H 62G>A UCEC-US 16 3828110 3828110 single base substitution C T missense_variant R634H 1901G>A UCEC-US 16 3828110 3828110 single base substitution C T missense_variant R672H 2015G>A UCEC-US 16 3828110 3828110 single base substitution C T upstream_gene_variant UCEC-US 16 3828768 3828768 single base substitution C T missense_variant R587H 1760G>A UCEC-US 16 3828768 3828768 single base substitution C T missense_variant R625H 1874G>A UCEC-US 16 3828768 3828768 single base substitution C T missense_variant R62H 185G>A UCEC-US 16 3828768 3828768 single base substitution C T upstream_gene_variant UCEC-US 16 3831269 3831269 single base substitution T G missense_variant T500P 1498A>C UCEC-US 16 3831269 3831269 single base substitution T G missense_variant T538P 1612A>C UCEC-US 16 3831269 3831269 single base substitution T G upstream_gene_variant UCEC-US 16 3843499 3843499 insertion of <=200bp - T frameshift_variant Q368Q? UCEC-US 16 3900321 3900321 single base substitution C T missense_variant A259T 775G>A UCEC-US 16 3900364 3900364 single base substitution C T synonymous_variant T244T 732G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 18T COSM109403 c.758A>T p.H253L Substitution - Missense 16:3850337-3850337 - TCGA-AP-A051-01 COSM970556 c.5044C>T p.R1682C Substitution - Missense 16:3731320-3731320 - LUAD-RT-S01832 COSM384618 c.424G>C p.G142R Substitution - Missense 16:3850671-3850671 - Pat_06_A COSM5850891 c.3841G>A p.V1281I Substitution - Missense 16:3745350-3745350 - SA214 COSM213966 c.3242G>A p.R1081H Substitution - Missense 16:3767728-3767728 - TCGA-06-0749 COSM2151925 c.1256G>A p.W419* Substitution - Nonsense 16:3792055-3792055 - PD6924a COSM4384864 c.6823G>A p.G2275R Substitution - Missense 16:3728224-3728224 - WT025 COSM5351901 c.5457C>A p.C1819* Substitution - Nonsense 16:3729590-3729590 - tumor_4177601 COSM166411 c.3836+1G>A p.? Unknown 16:3749626-3749626 - WA16 COSM237245 c.1389G>A p.G463G Substitution - coding silent 16:3782868-3782868 - 2209 COSM88755 c.223C>T p.R75* Substitution - Nonsense 16:3850872-3850872 - 177T COSM1726101 c.5399G>A p.R1800Q Substitution - Missense 16:3729648-3729648 - B37 COSM254627 c.310C>T p.Q104* Substitution - Nonsense 16:3850785-3850785 - 8066506 COSM3771943 c.4817A>G p.K1606R Substitution - Missense 16:3731849-3731849 - 9227_T COSM1377824 c.4506G>A p.W1502* Substitution - Nonsense 16:3736704-3736704 - ESCC_1 COSM5622421 c.2302C>T p.R768* Substitution - Nonsense 16:3773912-3773912 - B62-0 COSM254630 c.3323C>A p.S1108* Substitution - Nonsense 16:3758900-3758900 - M-07e COSM96470 c.6624A>C p.Q2208H Substitution - Missense 16:3728423-3728423 - DLBCL701 COSM1580738 c.4309A>T p.I1437F Substitution - Missense 16:3738644-3738644 - BN26 COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - FL26 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - S02242 COSM5663064 c.2464G>T p.G822* Substitution - Nonsense 16:3770986-3770986 - SJHYPO002 COSM4775397 c.1167_1184del18 p.N390_M395delNVLNHM Deletion - In frame 16:3793418-3793435 - TCGA-D7-8575-01 COSM4060703 c.4900G>A p.V1634M Substitution - Missense 16:3731464-3731464 - TCGA-FU-A3TX-01 COSM4849366 c.3779+1G>A p.? Unknown 16:3751725-3751725 - STC246 COSM1640477 c.3468C>T p.D1156D Substitution - coding silent 16:3757950-3757950 - 1524409 COSM96444 c.5660C>G p.S1887* Substitution - Nonsense 16:3729387-3729387 - B59 COSM254629 c.3217C>T p.Q1073* Substitution - Nonsense 16:3767753-3767753 - TCGA-BG-A18B-01 COSM970574 c.4211G>T p.G1404V Substitution - Missense 16:3739647-3739647 - LPJ128 COSM1316916 c.4414T>G p.W1472G Substitution - Missense 16:3736796-3736796 - UM-SCC-11B COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - TCGA-MY-A5BD-01 COSM4855569 c.386C>A p.S129* Substitution - Nonsense 16:3850709-3850709 - PD7017a COSM4384865 c.6364C>T p.Q2122* Substitution - Nonsense 16:3728683-3728683 - SJMB028 COSM255965 c.1447C>T p.R483* Substitution - Nonsense 16:3782810-3782810 - TCGA-AA-A010-01 COSM280130 c.4166T>C p.F1389S Substitution - Missense 16:3739692-3739692 - 104929 COSM95589 c.4735C>T p.Q1579* Substitution - Nonsense 16:3731931-3731931 - TCGA-AA-3525-01 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - 587376 COSM1202274 c.1855G>A p.A619T Substitution - Missense 16:3778786-3778786 - PD6171a COSM4384867 c.5545A>T p.K1849* Substitution - Nonsense 16:3729502-3729502 - 587284 COSM417011 c.4990C>T p.R1664C Substitution - Missense 16:3731374-3731374 - P62 COSM5009752 c.5444G>A p.G1815D Substitution - Missense 16:3729603-3729603 - CHEWS015 COSM4579030 c.6763C>T p.P2255S Substitution - Missense 16:3728284-3728284 - TCGA-D8-A27H-01 COSM1478866 c.5982G>C p.Q1994H Substitution - Missense 16:3729065-3729065 - OSCC-GB_00410111 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - B59-0 COSM1745405 c.2685delC p.Q897fs*30 Deletion - Frameshift 16:3770765-3770765 - B80-13-Tumor COSM254633 c.2515C>T p.Q839* Substitution - Nonsense 16:3770935-3770935 - RKO COSM2920019 c.2597T>C p.M866T Substitution - Missense 16:3770853-3770853 - SNU-C2B COSM2920065 c.617C>T p.A206V Substitution - Missense 16:3850478-3850478 - TCGA-D3-A1Q8-06 COSM3509563 c.2064G>A p.P688P Substitution - coding silent 16:3778060-3778060 - PAPJIB COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - tumor_4105105 COSM3356830 c.4293T>C p.I1431I Substitution - coding silent 16:3738660-3738660 - TCGA-HU-8602-01 COSM4060705 c.4740C>T p.G1580G Substitution - coding silent 16:3731926-3731926 - 39_FL COSM4170759 c.3982+2T>A p.? Unknown 16:3744892-3744892 - PD4877a COSM5025098 c.5790delC p.T1931fs*45 Deletion - Frameshift 16:3729257-3729257 - PD6116a COSM4384871 c.3484A>G p.N1162D Substitution - Missense 16:3757934-3757934 - 47_tFL COSM4170760 c.3061-2A>G p.? Unknown 16:3767911-3767911 - TCGA-31-1950-01 COSM70300 c.4358T>C p.I1453T Substitution - Missense 16:3738595-3738595 - LUAD-S01409 COSM346449 c.3452G>T p.W1151L Substitution - Missense 16:3757966-3757966 - TCGA-CC-5258-01 COSM4933407 c.2486T>C p.L829P Substitution - Missense 16:3770964-3770964 - T3091 COSM4674653 c.2237_2238insC p.M747fs*85 Insertion - Frameshift 16:3774614-3774615 - TCGA-AA-A010-01 COSM280129 c.4840T>C p.S1614P Substitution - Missense 16:3731826-3731826 - Gp2D COSM2919930 c.5410C>T p.H1804Y Substitution - Missense 16:3729637-3729637 - TCGA-DH-A66F-01 COSM3969560 c.1369A>G p.I457V Substitution - Missense 16:3782888-3782888 - KOPT-K1 COSM96462 c.5065C>T p.L1689F Substitution - Missense 16:3731299-3731299 - HCT-15 COSM1678808 c.3449C>A p.P1150H Substitution - Missense 16:3757969-3757969 - 292_T COSM3957565 c.4627G>T p.D1543Y Substitution - Missense 16:3736137-3736137 - 1781 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - T3090 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - tumor_4105105 COSM3356829 c.4301T>A p.L1434Q Substitution - Missense 16:3738652-3738652 - 471 COSM4437808 c.3874C>A p.Q1292K Substitution - Missense 16:3745317-3745317 - 4496 COSM5751280 c.4174C>CT p.R1392fs*9 Complex - frameshift 16:3739684-3739684 - ESCC_35 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-DK-A2I1-01 COSM1301961 c.1996G>C p.E666Q Substitution - Missense 16:3778128-3778128 - TCGA-CD-A4MG-01 COSM703031 c.3893A>G p.Y1298C Substitution - Missense 16:3745298-3745298 - 2_tFL COSM4170752 c.5040_5042delCTT p.L1681delL Deletion - In frame 16:3731322-3731324 - CHC1715T COSM4789576 c.501C>T p.A167A Substitution - coding silent 16:3850594-3850594 - B98 COSM1756924 c.6513G>A p.L2171L Substitution - coding silent 16:3728534-3728534 - ICGC_PA110 COSM3670194 c.5383T>C p.C1795R Substitution - Missense 16:3729664-3729664 - P134 COSM5010118 c.5408A>G p.Q1803R Substitution - Missense 16:3729639-3729639 - B109 COSM254625 c.4336C>G p.R1446G Substitution - Missense 16:3738617-3738617 - LUAD-S01357 COSM386711 c.3044G>T p.G1015V Substitution - Missense 16:3769190-3769190 - 258 COSM3732528 c.4396_4397insT p.Y1466fs*13 Insertion - Frameshift 16:3736813-3736814 - TCGA-BR-8360-01 COSM4060716 c.1893C>A p.A631A Substitution - coding silent 16:3778748-3778748 - KOPT-K1 COSM96459 c.2141G>A p.R714H Substitution - Missense 16:3777630-3777630 - PT49 COSM5936198 c.4295C>T p.S1432F Substitution - Missense 16:3738658-3738658 - T3225 COSM4674645 c.5954G>A p.R1985H Substitution - Missense 16:3729093-3729093 - CHC1715T COSM4789576 c.501C>T p.A167A Substitution - coding silent 16:3850594-3850594 - TCGA-AZ-4315-01 COSM1377858 c.1801C>T p.R601W Substitution - Missense 16:3780754-3780754 - SUDHL10 COSM88772 c.5831delC p.P1946fs*30 Deletion - Frameshift 16:3729216-3729216 - HCT116 COSM280131 c.270C>T p.S90S Substitution - coding silent 16:3850825-3850825 - BD59T COSM2920068 c.416G>A p.S139N Substitution - Missense 16:3850679-3850679 - HCC020T COSM5809132 c.6770A>T p.Q2257L Substitution - Missense 16:3728277-3728277 - 1524424 COSM96454 c.? p.? Unknown 2191 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - 1649669 COSM166406 c.4231G>A p.G1411R Substitution - Missense 16:3739627-3739627 - B89-4 COSM254635 c.1258A>T p.K420* Substitution - Nonsense 16:3792053-3792053 - B66-Tumor COSM254631 c.6983C>T p.S2328L Substitution - Missense 16:3728064-3728064 - CCK81 COSM2920044 c.1445A>G p.Q482R Substitution - Missense 16:3782812-3782812 - TCGA-BS-A0UF-01 COSM970578 c.3956G>A p.R1319Q Substitution - Missense 16:3744920-3744920 - TCGA-AP-A059-01 COSM970554 c.5124C>T p.N1708N Substitution - coding silent 16:3731240-3731240 - SJHGG019_S COSM4969328 c.4765delA p.N1589fs*46 Deletion - Frameshift 16:3731901-3731901 - S12-11594-TP COSM4990893 c.598C>T p.Q200* Substitution - Nonsense 16:3850497-3850497 - SC-her2-068 COSM2919997 c.3323C>T p.S1108L Substitution - Missense 16:3758900-3758900 - HN_62740 COSM126635 c.1507C>T p.Q503* Substitution - Nonsense 16:3782750-3782750 - PD23565a COSM5752819 c.3623_3624insC p.Q1209fs*25 Insertion - Frameshift 16:3757362-3757363 - TCGA-D8-A27G-01 COSM3817965 c.578C>G p.S193C Substitution - Missense 16:3850517-3850517 - TCGA-D1-A103-01 COSM970544 c.6424C>A p.L2142M Substitution - Missense 16:3728623-3728623 - 22T COSM107062 c.2126C>T p.S709F Substitution - Missense 16:3777645-3777645 - PT47 COSM5136933 c.3307C>T p.R1103* Substitution - Nonsense 16:3758916-3758916 - LUAD-RT-S01818 COSM383874 c.5603G>T p.R1868L Substitution - Missense 16:3729444-3729444 - TCGA-FD-A3N5-01 COSM1301962 c.235G>A p.G79S Substitution - Missense 16:3850860-3850860 - QC2-07-T2 COSM5652013 c.3915-1G>A p.? Unknown 16:3744962-3744962 - RK206_C01 COSM3741918 c.7082C>T p.S2361F Substitution - Missense 16:3727965-3727965 - TCGA-BS-A0TA-01 COSM970558 c.4996G>A p.A1666T Substitution - Missense 16:3731368-3731368 - CLL067 COSM1290518 c.6952C>G p.Q2318E Substitution - Missense 16:3728095-3728095 - BD180T COSM5495182 c.1052G>T p.R351L Substitution - Missense 16:3793550-3793550 - 86564 COSM95816 c.3546A>G p.A1182A Substitution - coding silent 16:3757872-3757872 - TCGA-AP-A059-01 COSM970572 c.4251C>A p.Y1417* Substitution - Nonsense 16:3739607-3739607 - 8030137 COSM1159410 c.1216G>C p.V406L Substitution - Missense 16:3793386-3793386 - DN12102 COSM5787046 c.4277C>T p.T1426M Substitution - Missense 16:3739581-3739581 - TCGA-G2-A2EO-01 COSM1301954 c.7302G>A p.T2434T Substitution - coding silent 16:3727745-3727745 - PT49 COSM5136933 c.3307C>T p.R1103* Substitution - Nonsense 16:3758916-3758916 - LB2518-MEL COSM21764 c.5271C>T p.G1757G Substitution - coding silent 16:3729776-3729776 - CLL44 COSM88754 c.4865A>G p.Y1622C Substitution - Missense 16:3731801-3731801 - T36 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - TCGA-HU-A4GX-01 COSM1478868 c.3271C>T p.R1091C Substitution - Missense 16:3758952-3758952 - 127T COSM5576002 c.712G>A p.V238M Substitution - Missense 16:3850383-3850383 - TARGET-20-PARCVS-03A-01D COSM5487609 c.1760_1761insG p.V588fs*20 Insertion - Frameshift 16:3780794-3780795 - I2L-P9-Tumor-Biopsy COSM1249109 c.4209C>T p.D1403D Substitution - coding silent 16:3739649-3739649 - ICGC_MB56 COSM166408 c.4471C>A p.Q1491K Substitution - Missense 16:3736739-3736739 - tumor_4125240 COSM1161163 c.4243C>T p.Q1415* Substitution - Nonsense 16:3739615-3739615 - 17_FL COSM4170756 c.4448T>A p.I1483N Substitution - Missense 16:3736762-3736762 - Au4 COSM4851689 c.4413C>G p.I1471M Substitution - Missense 16:3736797-3736797 - 41 COSM5015351 c.2863C>T p.Q955* Substitution - Nonsense 16:3770587-3770587 - 10539 COSM5751535 c.5799_5800insC p.S1934fs*32 Insertion - Frameshift 16:3729247-3729248 - TCGA-AD-5900-01 COSM1377810 c.7231delC p.Q2411fs*2 Deletion - Frameshift 16:3727816-3727816 - 2492729 COSM5725859 c.3060+1G>A p.? Unknown 16:3769173-3769173 - I2L-P7-Tumor-Organoid COSM5363732 c.4504T>C p.W1502R Substitution - Missense 16:3736706-3736706 - TCGA-24-0966-01 COSM74259 c.4013T>C p.L1338S Substitution - Missense 16:3740519-3740519 - TCGA-BR-8361-01 COSM4060694 c.6342C>T p.G2114G Substitution - coding silent 16:3728705-3728705 - DM34 COSM5608144 c.4971C>T p.S1657S Substitution - coding silent 16:3731393-3731393 - DM17 COSM5608139 c.5061C>T p.S1687S Substitution - coding silent 16:3731303-3731303 - QC2-20-T2 COSM5656319 c.5034_5036delCTC p.S1680delS Deletion - In frame 16:3731328-3731330 - 15_tFL COSM4170755 c.4450T>G p.F1484V Substitution - Missense 16:3736760-3736760 - ESCC_BICR_010T COSM5435932 c.6334C>G p.Q2112E Substitution - Missense 16:3728713-3728713 - TCGA-EE-A2GP-06 COSM3509568 c.852A>T p.G284G Substitution - coding silent 16:3810726-3810726 - 34t COSM88740 c.4427C>G p.P1476R Substitution - Missense 16:3736783-3736783 - BV-173 COSM96467 c.4873A>T p.M1625L Substitution - Missense 16:3731793-3731793 - GC8_T COSM148010 c.2784G>A p.P928P Substitution - coding silent 16:3770666-3770666 - SC-her2-035 COSM4777506 c.220C>G p.L74V Substitution - Missense 16:3850875-3850875 - 2152 COSM88756 c.286C>T p.Q96* Substitution - Nonsense 16:3850809-3850809 - TCGA-AA-3966-01 COSM272537 c.2516A>G p.Q839R Substitution - Missense 16:3770934-3770934 - tumor_4159170 COSM1161162 c.4508A>C p.Y1503S Substitution - Missense 16:3736702-3736702 - CHC1747T COSM4788085 c.4414T>A p.W1472R Substitution - Missense 16:3736796-3736796 - B109 COSM254625 c.4336C>G p.R1446G Substitution - Missense 16:3738617-3738617 - PT15_1 COSM5897923 c.4118C>T p.P1373L Substitution - Missense 16:3740414-3740414 - T3340 COSM4674646 c.4327C>T p.R1443C Substitution - Missense 16:3738626-3738626 - CHC917T COSM3667851 c.6012A>T p.R2004R Substitution - coding silent 16:3729035-3729035 - Pat_66_A COSM5850897 c.824C>T p.P275L Substitution - Missense 16:3810754-3810754 - TCGA-F1-6874-01 COSM2920017 c.2615C>T p.T872M Substitution - Missense 16:3770835-3770835 - TCGA-FU-A3HZ-01 COSM3420984 c.212C>T p.S71L Substitution - Missense 16:3850883-3850883 - TCGA-A5-A0G9-01 COSM970612 c.775G>A p.A259T Substitution - Missense 16:3850320-3850320 - 101 COSM3402318 c.4039C>T p.R1347W Substitution - Missense 16:3740493-3740493 - LP6005500-DNA_D01 COSM5036155 c.1703C>G p.S568C Substitution - Missense 16:3780852-3780852 - TCGA-AA-3695-01 COSM293366 c.2178C>T p.P726P Substitution - coding silent 16:3774674-3774674 - TCGA-61-1740-01 COSM1324453 c.3911_3914+10delCAGGGTGAGTTGTT p.? Unknown 16:3745267-3745280 - TCGA-HJ-7597-01 COSM4060718 c.1187C>T p.T396M Substitution - Missense 16:3793415-3793415 - TARGET-20-PANGJY-09A-03D COSM5487399 c.5436C>T p.T1812T Substitution - coding silent 16:3729611-3729611 - 2492703 COSM5599342 c.7047C>T p.V2349V Substitution - coding silent 16:3728000-3728000 - 2073443 COSM1735705 c.? p.E1035* Substitution - Nonsense RPMI-8402 COSM96471 c.6938C>T p.P2313L Substitution - Missense 16:3728109-3728109 - tumor_4166503 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-AZ-6601-01 COSM1377854 c.2517G>T p.Q839H Substitution - Missense 16:3770933-3770933 - P111 COSM1736424 c.1945G>A p.E649K Substitution - Missense 16:3778179-3778179 - 403 COSM2920056 c.1123G>T p.G375* Substitution - Nonsense 16:3793479-3793479 - CSCC-44-T COSM4544795 c.3645G>A p.G1215G Substitution - coding silent 16:3757341-3757341 - ESCC_6 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - PD12803a COSM3770093 c.5293C>T p.Q1765* Substitution - Nonsense 16:3729754-3729754 - B63 COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - CSCC-27-T COSM4502816 c.6237C>T p.S2079S Substitution - coding silent 16:3728810-3728810 - HN_62739 COSM122354 c.4561G>T p.D1521Y Substitution - Missense 16:3736203-3736203 - H1048 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - SUDHL7 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - SNU-175 COSM4650376 c.6709C>A p.P2237T Substitution - Missense 16:3728338-3728338 - ESCC-F92 COSM5049061 c.3414C>G p.I1138M Substitution - Missense 16:3758004-3758004 - ICGC_0060 COSM1159410 c.1216G>C p.V406L Substitution - Missense 16:3793386-3793386 - TCGA-B5-A11Y-01 COSM970552 c.5344G>A p.A1782T Substitution - Missense 16:3729703-3729703 - TCGA-EK-A2RC-01 COSM4848624 c.3955C>T p.R1319* Substitution - Nonsense 16:3744921-3744921 - TCGA-BR-4201-01 COSM4060720 c.535G>A p.A179T Substitution - Missense 16:3850560-3850560 - TCGA-CH-5748-01 COSM1128960 c.4455T>C p.H1485H Substitution - coding silent 16:3736755-3736755 - DM29 COSM5608142 c.1899T>C p.A633A Substitution - coding silent 16:3778742-3778742 - CHC892T COSM4961351 c.6292G>A p.A2098T Substitution - Missense 16:3728755-3728755 - 2524310 COSM1238064 c.? p.? Unknown HCC35T COSM1609322 c.1647_1654delAGCTCTTC p.A550fs*18 Deletion - Frameshift 16:3781226-3781233 - SW403 COSM4260257 c.687A>T p.P229P Substitution - coding silent 16:3850408-3850408 - TCGA-IR-A3LK-01 COSM4414487 c.95C>T p.S32L Substitution - Missense 16:3851000-3851000 - CHC121T COSM3667852 c.2977C>T p.P993S Substitution - Missense 16:3769257-3769257 - ICGC_MB60 COSM3764561 c.3599G>A p.C1200Y Substitution - Missense 16:3757819-3757819 - MN-296 COSM1578556 c.2491_2497delAACCCTC p.N831fs*16 Deletion - Frameshift 16:3770953-3770959 - 1968392 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - CSCC-16-T COSM4589684 c.4478_4479insA p.P1494fs*25 Insertion - Frameshift 16:3736731-3736732 - SH-102782 COSM5021088 c.5052C>T p.S1684S Substitution - coding silent 16:3731312-3731312 - CRC-02T COSM5454450 c.7023C>A p.N2341K Substitution - Missense 16:3728024-3728024 - 4-1030604-T1 COSM88760 c.3517C>T p.R1173* Substitution - Nonsense 16:3757901-3757901 - LUAD-E00897 COSM364389 c.1844C>T p.T615I Substitution - Missense 16:3778797-3778797 - BL3 COSM1161163 c.4243C>T p.Q1415* Substitution - Nonsense 16:3739615-3739615 - WSU-HN12 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - BD72T COSM260287 c.5470G>A p.A1824T Substitution - Missense 16:3729577-3729577 - T1743 COSM2919940 c.5139C>T p.H1713H Substitution - coding silent 16:3731225-3731225 - 103591 COSM94089 c.7130C>T p.S2377L Substitution - Missense 16:3727917-3727917 - CH-60-T2 COSM5651302 c.4451T>G p.F1484C Substitution - Missense 16:3736759-3736759 - ESCC_47 COSM5630720 c.2311C>A p.Q771K Substitution - Missense 16:3773903-3773903 - B110-Tumor COSM88756 c.286C>T p.Q96* Substitution - Nonsense 16:3850809-3850809 - 2043 COSM96481 c.?_?del? p.? Unknown B105-0 COSM1745389 c.4300_4325del26 p.L1434fs*10 Deletion - Frameshift 16:3738628-3738653 - TCGA-EE-A184-06 COSM3509552 c.6055G>T p.G2019W Substitution - Missense 16:3728992-3728992 - 6P2-1 COSM3734328 c.6484G>C p.G2162R Substitution - Missense 16:3728563-3728563 - AD76 COSM5966846 c.58C>A p.P20T Substitution - Missense 16:3879859-3879859 - tumor_4115001 COSM5947555 c.4391T>A p.L1464* Substitution - Nonsense 16:3738562-3738562 - 1526884 COSM96515 c.? p.? Unknown SNU-C2B COSM4651265 c.6033C>T p.P2011P Substitution - coding silent 16:3729014-3729014 - S06-38853-TP COSM4990887 c.3004C>T p.Q1002* Substitution - Nonsense 16:3769230-3769230 - CHC304T COSM4788451 c.4157C>G p.S1386C Substitution - Missense 16:3739701-3739701 - RMS2049 COSM5880665 c.346A>G p.S116G Substitution - Missense 16:3850749-3850749 - 166T COSM5576101 c.2181G>A p.M727I Substitution - Missense 16:3774671-3774671 - OVCAR5 COSM96416 c.3211G>A p.A1071T Substitution - Missense 16:3767759-3767759 - 53M COSM3888515 c.3840C>T p.F1280F Substitution - coding silent 16:3745351-3745351 - HCC53T COSM1609323 c.1460C>A p.A487D Substitution - Missense 16:3782797-3782797 - tumor_4113191 COSM88745 c.4508A>T p.Y1503F Substitution - Missense 16:3736702-3736702 - S02-15015-TP COSM4990882 c.4278G>A p.T1426T Substitution - coding silent 16:3739580-3739580 - TCGA-AA-3713-01 COSM3690996 c.5796G>T p.T1932T Substitution - coding silent 16:3729251-3729251 - 2492701 COSM5599342 c.7047C>T p.V2349V Substitution - coding silent 16:3728000-3728000 - B105 COSM88760 c.3517C>T p.R1173* Substitution - Nonsense 16:3757901-3757901 - 1524424 COSM96446 c.? p.L470* Substitution - Nonsense 1524373 COSM96481 c.?_?del? p.? Unknown 2075 COSM96481 c.?_?del? p.? Unknown TCGA-GN-A26C-01 COSM3509558 c.2978C>A p.P993H Substitution - Missense 16:3769256-3769256 - 103515 COSM95817 c.1557G>A p.R519R Substitution - coding silent 16:3782700-3782700 - BICR_22 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - 34_tFL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-39-5031-01 COSM703038 c.6943A>T p.S2315C Substitution - Missense 16:3728104-3728104 - ATL020 COSM5706124 c.6893A>G p.Q2298R Substitution - Missense 16:3728154-3728154 - tumor_4145056 COSM5363732 c.4504T>C p.W1502R Substitution - Missense 16:3736706-3736706 - SJHYPO040 COSM4775684 c.3833_3836+19del23 p.? Unknown 16:3749608-3749630 - 587256 COSM970552 c.5344G>A p.A1782T Substitution - Missense 16:3729703-3729703 - CSCC-31-T COSM4545799 c.3867G>A p.K1289K Substitution - coding silent 16:3745324-3745324 - S00936 COSM317185 c.4280+2T>C p.? Unknown 16:3739576-3739576 - SE2 COSM970536 c.7089G>A p.P2363P Substitution - coding silent 16:3727958-3727958 - TCGA-AP-A056-01 COSM970576 c.4034T>G p.F1345C Substitution - Missense 16:3740498-3740498 - TCGA-AA-A01Z-01 COSM300410 c.4893C>A p.V1631V Substitution - coding silent 16:3731471-3731471 - TCGA-66-2795-01 COSM703025 c.1847C>G p.P616R Substitution - Missense 16:3778794-3778794 - TCGA-46-6025-01 COSM703028 c.2441C>T p.P814L Substitution - Missense 16:3773773-3773773 - YUDEXA COSM1708693 c.3394C>T p.P1132S Substitution - Missense 16:3758024-3758024 - LC_S13 COSM1191083 c.3883_3884insT p.L1296fs*4 Insertion - Frameshift 16:3745307-3745308 - TCGA-AA-3818-01 COSM270820 c.5424C>A p.C1808* Substitution - Nonsense 16:3729623-3729623 - I2L-P19Ta-Tumor-Organoid COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - tumor_4128477 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-BP-4331-01 COSM3361760 c.3622C>A p.P1208T Substitution - Missense 16:3757364-3757364 - TCGA-D1-A16J-01 COSM970586 c.3299C>A p.A1100E Substitution - Missense 16:3758924-3758924 - TCGA-18-3412-01 COSM703040 c.7152C>A p.H2384Q Substitution - Missense 16:3727895-3727895 - QC2-20-T2 COSM5656318 c.1942-1G>A p.? Unknown 16:3778183-3778183 - TCGA-EE-A2MI-06 COSM3509571 c.258A>T p.I86I Substitution - coding silent 16:3850837-3850837 - LUAD-B00416 COSM330979 c.7285G>T p.D2429Y Substitution - Missense 16:3727762-3727762 - 2_tFL COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - 1649669 COSM166407 c.4262G>A p.C1421Y Substitution - Missense 16:3739596-3739596 - 33 COSM4169928 c.3671A>G p.D1224G Substitution - Missense 16:3757315-3757315 - FL15 COSM88738 c.4337G>T p.R1446L Substitution - Missense 16:3738616-3738616 - 3N43-VS-3T43 COSM4982033 c.3198C>T p.S1066S Substitution - coding silent 16:3767772-3767772 - CHC1744T COSM4792357 c.3719G>A p.C1240Y Substitution - Missense 16:3751786-3751786 - 12T COSM106942 c.7318G>A p.E2440K Substitution - Missense 16:3727729-3727729 - TCGA-EE-A2MR-06 COSM3509570 c.391C>T p.P131S Substitution - Missense 16:3850704-3850704 - 2164865 COSM3736955 c.4298A>G p.Y1433C Substitution - Missense 16:3738655-3738655 - 10 COSM5762852 c.6980C>T p.A2327V Substitution - Missense 16:3728067-3728067 - 2015 COSM88743 c.4507T>G p.Y1503D Substitution - Missense 16:3736703-3736703 - TL20 COSM5751709 c.2272_2273insA p.S758fs*74 Insertion - Frameshift 16:3774579-3774580 - TCGA-EE-A2GR-06 COSM3509559 c.2963C>T p.P988L Substitution - Missense 16:3769271-3769271 - B62-0 COSM254630 c.3323C>A p.S1108* Substitution - Nonsense 16:3758900-3758900 - ESCC_BICR_012T COSM5433071 c.5029G>A p.E1677K Substitution - Missense 16:3731335-3731335 - B80-13 COSM254633 c.2515C>T p.Q839* Substitution - Nonsense 16:3770935-3770935 - PD7726a COSM5945319 c.1780G>T p.E594* Substitution - Nonsense 16:3780775-3780775 - S02-14875-TP COSM4990891 c.1489C>T p.Q497* Substitution - Nonsense 16:3782768-3782768 - PAPLDL COSM5004450 c.4322G>C p.R1441P Substitution - Missense 16:3738631-3738631 - ESCC_4 COSM5622779 c.1909G>C p.E637Q Substitution - Missense 16:3778732-3778732 - FL22 COSM88747 c.4304A>G p.D1435G Substitution - Missense 16:3738649-3738649 - HCC41T COSM1609321 c.2284-5C>G p.? Unknown 16:3773935-3773935 - TCGA-25-1631-01 COSM79348 c.4021C>T p.R1341* Substitution - Nonsense 16:3740511-3740511 - DLBCL832 COSM88745 c.4508A>T p.Y1503F Substitution - Missense 16:3736702-3736702 - T3094 COSM4674637 c.7175C>T p.A2392V Substitution - Missense 16:3727872-3727872 - HCC49 COSM1609324 c.234C>T p.S78S Substitution - coding silent 16:3850861-3850861 - TCGA-D1-A15X-01 COSM970588 c.3114A>G p.I1038M Substitution - Missense 16:3767856-3767856 - PD3186a COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - CLL103 COSM1290519 c.35C>A p.P12H Substitution - Missense 16:3879882-3879882 - tumor_4124542 COSM3356828 c.4463C>T p.P1488L Substitution - Missense 16:3736747-3736747 - QC2-32-T2 COSM5656319 c.5034_5036delCTC p.S1680delS Deletion - In frame 16:3731328-3731330 - TCGA-EA-A3QD-01 COSM4821768 c.5277A>T p.P1759P Substitution - coding silent 16:3729770-3729770 - SA214 COSM212243 c.3334C>T p.R1112W Substitution - Missense 16:3758889-3758889 - TCGA-BR-8382-01 COSM1202269 c.6596A>T p.Q2199L Substitution - Missense 16:3728451-3728451 - 53M COSM2919944 c.5039C>T p.S1680F Substitution - Missense 16:3731325-3731325 - ICGC_0034 COSM218493 c.2950A>C p.N984H Substitution - Missense 16:3769284-3769284 - S12-11594-TP COSM4990892 c.931C>T p.P311S Substitution - Missense 16:3810647-3810647 - NB07C COSM1236407 c.4681G>T p.E1561* Substitution - Nonsense 16:3736083-3736083 - ESCC_164 COSM5648206 c.324C>A p.N108K Substitution - Missense 16:3850771-3850771 - TCGA-MI-A75G-01 COSM4940015 c.973A>T p.M325L Substitution - Missense 16:3810605-3810605 - TCGA-AP-A056-01 COSM970592 c.2708C>A p.P903H Substitution - Missense 16:3770742-3770742 - TCGA-AO-A128-01 COSM3817960 c.6803T>C p.M2268T Substitution - Missense 16:3728244-3728244 - PD23565a COSM5802063 c.3622_3623insC p.Q1209fs*25 Insertion - Frameshift 16:3757363-3757364 - Pat_05_B COSM5850892 c.3023_3024CC>TT p.P1008L Substitution - Missense 16:3769210-3769211 - 677-07-01TD COSM5419554 c.3247A>T p.K1083* Substitution - Nonsense 16:3767723-3767723 - T3446 COSM4674644 c.6132C>A p.A2044A Substitution - coding silent 16:3728915-3728915 - TCGA-RP-A695-06 COSM4896231 c.7323C>T p.G2441G Substitution - coding silent 16:3727724-3727724 - TCGA-13-0724-01 COSM69054 c.2509_2515delGGGCCTC p.G837fs*10 Deletion - Frameshift 16:3770935-3770941 - WSU-HN13 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - RA37T COSM1737915 c.3689A>C p.Y1230S Substitution - Missense 16:3757297-3757297 - TCGA-B7-5816-01 COSM4060695 c.6253C>T p.Q2085* Substitution - Nonsense 16:3728794-3728794 - MedB-1 COSM5620544 c.4345G>A p.V1449I Substitution - Missense 16:3738608-3738608 - ML_77_T_01 COSM5034000 c.5838A>C p.P1946P Substitution - coding silent 16:3729209-3729209 - tumor_4175837 COSM88743 c.4507T>G p.Y1503D Substitution - Missense 16:3736703-3736703 - PD8934a COSM4384869 c.4640A>G p.N1547S Substitution - Missense 16:3736124-3736124 - DLD1 COSM4623334 c.1065G>A p.Q355Q Substitution - coding silent 16:3793537-3793537 - HCC030T COSM5658750 c.1942-2A>G p.? Unknown 16:3778184-3778184 - 1524381 COSM96445 c.4689G>C p.R1563S Substitution - Missense 16:3736075-3736075 - tumor_4103141 COSM5949821 c.3609G>A p.K1203K Substitution - coding silent 16:3757809-3757809 - TCGA-C4-A0F1-01 COSM417011 c.4990C>T p.R1664C Substitution - Missense 16:3731374-3731374 - T3202 COSM260287 c.5470G>A p.A1824T Substitution - Missense 16:3729577-3729577 - HCC079T COSM5808005 c.663A>T p.G221G Substitution - coding silent 16:3850432-3850432 - TCGA-GV-A3QG-01 COSM1301958 c.3427G>C p.D1143H Substitution - Missense 16:3757991-3757991 - LUAD-NYU408 COSM392000 c.4887_4888delGG p.E1630fs*29 Deletion - Frameshift 16:3731778-3731779 - QC2-20-T2 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - T3225 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - LOVO COSM2920037 c.1717A>G p.T573A Substitution - Missense 16:3780838-3780838 - TCGA-HF-7132-01 COSM4060689 c.7285G>A p.D2429N Substitution - Missense 16:3727762-3727762 - OV207 COSM252981 c.3370-4delT p.? Unknown 16:3758052-3758052 - 2334202 COSM260287 c.5470G>A p.A1824T Substitution - Missense 16:3729577-3729577 - 1514 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - DLBCL-PatientL COSM221505 c.3310C>T p.Q1104* Substitution - Nonsense 16:3758913-3758913 - CoCM-1 COSM4621018 c.6292G>T p.A2098S Substitution - Missense 16:3728755-3728755 - CSCC-16-T COSM4490056 c.3570C>T p.D1190D Substitution - coding silent 16:3757848-3757848 - QC2-05-T2 COSM5652006 c.3234_3250+31del48 p.? Unknown 16:3767689-3767736 - TCGA-AG-A002-01 COSM260287 c.5470G>A p.A1824T Substitution - Missense 16:3729577-3729577 - PD6098a COSM221505 c.3310C>T p.Q1104* Substitution - Nonsense 16:3758913-3758913 - RIVA COSM88763 c.4078C>T p.R1360* Substitution - Nonsense 16:3740454-3740454 - N-Thy002 COSM5094765 c.1040_1041delAT p.D347fs*2 Deletion - Frameshift 16:3793561-3793562 - DM10 COSM5608137 c.2012C>A p.S671* Substitution - Nonsense 16:3778112-3778112 - BD57T COSM5510778 c.1149G>A p.P383P Substitution - coding silent 16:3793453-3793453 - LPJ021 COSM1315875 c.4445A>G p.Y1482C Substitution - Missense 16:3736765-3736765 - S03-45671-TP COSM4990880 c.6498C>T p.P2166P Substitution - coding silent 16:3728549-3728549 - PD9694a COSM703029 c.2827C>T p.Q943* Substitution - Nonsense 16:3770623-3770623 - TCGA-AN-A0AR-01 COSM5833082 c.6150_6151insG p.P2051fs*290 Insertion - Frameshift 16:3728896-3728897 - TL42 COSM5751858 c.2701_2702insA p.P901fs*69 Insertion - Frameshift 16:3770748-3770749 - TCGA-BR-6566-01 COSM1159754 c.4492C>T p.R1498* Substitution - Nonsense 16:3736718-3736718 - OSCC-GB_00750111 COSM4891091 c.7098G>A p.R2366R Substitution - coding silent 16:3727949-3727949 - I2L-P19Ta-Tumor-Organoid COSM2920035 c.1802G>A p.R601Q Substitution - Missense 16:3780753-3780753 - B80-13 COSM254633 c.2515C>T p.Q839* Substitution - Nonsense 16:3770935-3770935 - TCGA-G2-A2EL-01 COSM1301957 c.4505G>A p.W1502* Substitution - Nonsense 16:3736705-3736705 - 9906_124 COSM303848 c.5367C>A p.N1789K Substitution - Missense 16:3729680-3729680 - 06-24881 COSM220500 c.4873A>G p.M1625V Substitution - Missense 16:3731793-3731793 - ov51 COSM96414 c.4061C>T p.A1354V Substitution - Missense 16:3740471-3740471 - TCGA-66-2742-01 COSM703027 c.2331T>C p.G777G Substitution - coding silent 16:3773883-3773883 - B66 COSM254632 c.3689A>G p.Y1230C Substitution - Missense 16:3757297-3757297 - B110 COSM96415 c.5932A>G p.N1978D Substitution - Missense 16:3729115-3729115 - 2134 COSM88741 c.4444T>C p.Y1482H Substitution - Missense 16:3736766-3736766 - TCGA-CH-5788-01 COSM1128962 c.6795G>A p.A2265A Substitution - coding silent 16:3728252-3728252 - TCGA-DK-A1AD-01 COSM1301956 c.4617T>G p.Y1539* Substitution - Nonsense 16:3736147-3736147 - pfg008T COSM1640477 c.3468C>T p.D1156D Substitution - coding silent 16:3757950-3757950 - B89-4 COSM254634 c.3779+1G>T p.? Unknown 16:3751725-3751725 - TCGA-09-2049-01 COSM79693 c.4401G>C p.V1467V Substitution - coding silent 16:3736809-3736809 - TCGA-BR-8690-01 COSM4060708 c.4412T>A p.I1471N Substitution - Missense 16:3736798-3736798 - OVCAR-8 COSM1678809 c.2678C>A p.S893* Substitution - Nonsense 16:3770772-3770772 - S17_post COSM5574530 c.5888A>G p.E1963G Substitution - Missense 16:3729159-3729159 - ESO-0009 COSM1249109 c.4209C>T p.D1403D Substitution - coding silent 16:3739649-3739649 - TCGA-C5-A2LX-01 COSM220498 c.4463C>G p.P1488R Substitution - Missense 16:3736747-3736747 - SK00102_M COSM79348 c.4021C>T p.R1341* Substitution - Nonsense 16:3740511-3740511 - LUAD-S01345 COSM396944 c.2499C>G p.L833L Substitution - coding silent 16:3770951-3770951 - S00935 COSM166408 c.4471C>A p.Q1491K Substitution - Missense 16:3736739-3736739 - B66-Tumor COSM254632 c.3689A>G p.Y1230C Substitution - Missense 16:3757297-3757297 - YUKSI COSM5384869 c.6490C>T p.L2164L Substitution - coding silent 16:3728557-3728557 - 3844_T COSM3957563 c.5604G>A p.R1868R Substitution - coding silent 16:3729443-3729443 - TCGA-60-2719-01 COSM703026 c.2103G>A p.V701V Substitution - coding silent 16:3778021-3778021 - PASFXA COSM5005801 c.3723C>T p.F1241F Substitution - coding silent 16:3751782-3751782 - T3080 COSM4674641 c.6548C>T p.A2183V Substitution - Missense 16:3728499-3728499 - PR-09-5094 COSM242504 c.3461T>C p.V1154A Substitution - Missense 16:3757957-3757957 - CMLPh-001 COSM4384868 c.5234G>A p.W1745* Substitution - Nonsense 16:3729813-3729813 - tumor_4110378 COSM5946446 c.3988C>T p.Q1330* Substitution - Nonsense 16:3740544-3740544 - 2183 COSM88766 c.1334_1335insCCAT p.L446fs*7 Insertion - Frameshift 16:3782922-3782923 - QC2-03-T2 COSM5656297 c.3373_3374delTA p.Y1125fs*2 Deletion - Frameshift 16:3758044-3758045 - QC2-12-T2 COSM5656310 c.4478T>A p.I1493K Substitution - Missense 16:3736732-3736732 - PD3195a COSM1658798 c.4051delC p.H1351fs*25 Deletion - Frameshift 16:3740481-3740481 - QC2-42-T2 COSM1316076 c.4303G>A p.D1435N Substitution - Missense 16:3738650-3738650 - NCI-H835 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 1524413 COSM96443 c.4499A>C p.Q1500P Substitution - Missense 16:3736711-3736711 - 380 COSM96469 c.5933A>G p.N1978S Substitution - Missense 16:3729114-3729114 - SNU_19_S1 COSM4420002 c.6551G>A p.S2184N Substitution - Missense 16:3728496-3728496 - WSU-HN8 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - 12-P8001 COSM4579032 c.3611A>T p.Y1204F Substitution - Missense 16:3757375-3757375 - HN_62897 COSM122356 c.760G>C p.A254P Substitution - Missense 16:3850335-3850335 - SJRHB024 COSM3737590 c.152T>G p.L51* Substitution - Nonsense 16:3850943-3850943 - S00539 COSM317183 c.3697A>T p.R1233W Substitution - Missense 16:3757289-3757289 - B66 COSM254632 c.3689A>G p.Y1230C Substitution - Missense 16:3757297-3757297 - TCGA-21-1081-01 COSM703031 c.3893A>G p.Y1298C Substitution - Missense 16:3745298-3745298 - 2492702 COSM5599342 c.7047C>T p.V2349V Substitution - coding silent 16:3728000-3728000 - 443 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - MT-260-T2 COSM5651493 c.4445A>C p.Y1482S Substitution - Missense 16:3736765-3736765 - 05-24006 COSM88752 c.4496T>C p.L1499P Substitution - Missense 16:3736714-3736714 - GB07 COSM1743091 c.3205G>C p.G1069R Substitution - Missense 16:3767765-3767765 - RK220_C01 COSM3741919 c.1941+2T>C p.? Unknown 16:3778698-3778698 - LS411 COSM2919907 c.6213G>A p.L2071L Substitution - coding silent 16:3728834-3728834 - TCGA-DG-A2KM-01 COSM4851689 c.4413C>G p.I1471M Substitution - Missense 16:3736797-3736797 - NOKSI COSM4595334 c.5264_5283del20 p.S1755fs*204 Deletion - Frameshift 16:3729764-3729783 - LUAD-B00523 COSM331816 c.6689A>G p.Q2230R Substitution - Missense 16:3728358-3728358 - 1649666 COSM166405 c.4232G>A p.G1411E Substitution - Missense 16:3739626-3739626 - TCGA-D8-A1XK-01 COSM3817962 c.4864T>C p.Y1622H Substitution - Missense 16:3731802-3731802 - SPEC1187 COSM220499 c.4444T>A p.Y1482N Substitution - Missense 16:3736766-3736766 - S00188 COSM5700965 c.4355A>T p.E1452V Substitution - Missense 16:3738598-3738598 - 251 COSM1741884 c.3251-4G>A p.? Unknown 16:3758976-3758976 - TCGA-AP-A051-01 COSM970580 c.3737G>A p.G1246D Substitution - Missense 16:3751768-3751768 - 2228003 COSM1238064 c.? p.? Unknown TCGA-FW-A3R5-06 COSM88763 c.4078C>T p.R1360* Substitution - Nonsense 16:3740454-3740454 - 23_FL COSM4170753 c.4501_4503delGAG p.E1501delE Deletion - In frame 16:3736707-3736709 - T3090 COSM4674638 c.7150delC p.H2384fs*12 Deletion - Frameshift 16:3727897-3727897 - 10-654 COSM1645445 c.2455G>A p.V819M Substitution - Missense 16:3773759-3773759 - AOCS-060-1-5 COSM3948542 c.7215G>T p.Q2405H Substitution - Missense 16:3727832-3727832 - TCGA-AU-6004-01 COSM1202269 c.6596A>T p.Q2199L Substitution - Missense 16:3728451-3728451 - tumor_4134005 COSM5949890 c.4944delC p.I1649fs*95 Deletion - Frameshift 16:3731420-3731420 - 8057700 COSM4388026 c.5267A>G p.Q1756R Substitution - Missense 16:3729780-3729780 - TCGA-EE-A2GI-06 COSM3509550 c.7005C>T p.I2335I Substitution - coding silent 16:3728042-3728042 - K116 COSM249379 c.5418G>C p.K1806N Substitution - Missense 16:3729629-3729629 - B89-4 COSM254634 c.3779+1G>T p.? Unknown 16:3751725-3751725 - LOVO COSM2919915 c.5717delC p.P1906fs*9 Deletion - Frameshift 16:3729330-3729330 - H7 COSM1238064 c.? p.? Unknown DM36 COSM5608145 c.690C>T p.A230A Substitution - coding silent 16:3850405-3850405 - PD7103a COSM4384873 c.868G>A p.A290T Substitution - Missense 16:3810710-3810710 - 4043 COSM5751227 c.6141_6142insA p.V2048fs*293 Insertion - Frameshift 16:3728905-3728906 - 20_tFL COSM4170758 c.4112T>A p.V1371D Substitution - Missense 16:3740420-3740420 - TCGA-BS-A0UV-01 COSM970548 c.6281C>T p.P2094L Substitution - Missense 16:3728766-3728766 - TCGA-18-3419-01 COSM703039 c.6989T>G p.L2330R Substitution - Missense 16:3728058-3728058 - T3658 COSM4674655 c.1669G>A p.A557T Substitution - Missense 16:3781211-3781211 - TCGA-29-1705-01 COSM1324452 c.1170C>G p.N390K Substitution - Missense 16:3793432-3793432 - TCGA-76-4925-01 COSM3402318 c.4039C>T p.R1347W Substitution - Missense 16:3740493-3740493 - SW403 COSM4655243 c.2325G>A p.M775I Substitution - Missense 16:3773889-3773889 - OSCC-GB_01090111 COSM4886380 c.5693G>T p.S1898I Substitution - Missense 16:3729354-3729354 - 203T COSM1377820 c.4837G>A p.V1613M Substitution - Missense 16:3731829-3731829 - HCC41 COSM1609321 c.2284-5C>G p.? Unknown 16:3773935-3773935 - 1524434 COSM96450 c.? p.R386* Substitution - Nonsense TCGA-34-2600-01 COSM703024 c.1810C>T p.L604L Substitution - coding silent 16:3780745-3780745 - 4_tFL COSM4170754 c.4451T>C p.F1484S Substitution - Missense 16:3736759-3736759 - SC-her2-038 COSM4777507 c.6569G>A p.R2190Q Substitution - Missense 16:3728478-3728478 - 2_FL COSM4170752 c.5040_5042delCTT p.L1681delL Deletion - In frame 16:3731322-3731324 - 2069 COSM88771 c.4707_4708insGCACT p.A1571fs*66 Insertion - Frameshift 16:3736056-3736057 - TCGA-04-1350-01 COSM117417 c.2650G>A p.A884T Substitution - Missense 16:3770800-3770800 - 2026 COSM88736 c.4022G>A p.R1341Q Substitution - Missense 16:3740510-3740510 - 2147 COSM96542 c.?_?del? p.? Unknown TCGA-DA-A1HV-06 COSM3509560 c.2782C>T p.P928S Substitution - Missense 16:3770668-3770668 - TCGA-D3-A51G-06 COSM3509555 c.3979A>T p.K1327* Substitution - Nonsense 16:3744897-3744897 - S01728 COSM317186 c.1157_1158insCATTGTCG p.T387fs*5 Insertion - Frameshift 16:3793444-3793445 - PD23579a COSM5752622 c.2461C>T p.Q821* Substitution - Nonsense 16:3773753-3773753 - SC_9058 COSM5567769 c.7066T>C p.S2356P Substitution - Missense 16:3727981-3727981 - MKB-1 COSM96458 c.7105C>A p.P2369T Substitution - Missense 16:3727942-3727942 - CHC304T COSM4788451 c.4157C>G p.S1386C Substitution - Missense 16:3739701-3739701 - PT35 COSM5913754 c.4678G>A p.E1560K Substitution - Missense 16:3736086-3736086 - TCGA-18-3408-01 COSM703030 c.3419G>A p.R1140Q Substitution - Missense 16:3757999-3757999 - CSCC-11-T COSM4537527 c.2431G>A p.G811R Substitution - Missense 16:3773783-3773783 - Pat_41_B COSM5850894 c.2654C>T p.P885L Substitution - Missense 16:3770796-3770796 - ESCC-F96 COSM5049210 c.573T>A p.S191R Substitution - Missense 16:3850522-3850522 - TCGA-LP-A4AV-01 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - tumor_4147081 COSM88741 c.4444T>C p.Y1482H Substitution - Missense 16:3736766-3736766 - Sample_1 COSM5021858 c.2129T>C p.L710P Substitution - Missense 16:3777642-3777642 - TCGA-BR-6452-01 COSM4060693 c.6431C>T p.A2144V Substitution - Missense 16:3728616-3728616 - TCGA-AU-6004-01 COSM1377813 c.5770G>A p.V1924M Substitution - Missense 16:3729277-3729277 - TCGA-AN-A046-01 COSM3817963 c.4175G>A p.R1392Q Substitution - Missense 16:3739683-3739683 - HPB-ALL COSM96468 c.(5830_5832)insC p.?fs Insertion - Frameshift S01728 COSM5679514 c.4237C>T p.H1413Y Substitution - Missense 16:3739621-3739621 - TCGA-A8-A09Z-01 COSM3817964 c.3860G>A p.G1287D Substitution - Missense 16:3745331-3745331 - FL6 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-BS-A0UF-01 COSM970598 c.2140C>T p.R714C Substitution - Missense 16:3777631-3777631 - 17_tFL COSM4170756 c.4448T>A p.I1483N Substitution - Missense 16:3736762-3736762 - 2492714 COSM5606450 c.3862C>T p.R1288W Substitution - Missense 16:3745329-3745329 - TCGA-FS-A1ZP-06 COSM3509562 c.2122C>T p.L708L Substitution - coding silent 16:3777649-3777649 - TCGA-06-2558 COSM2152630 c.5266_5267delCA p.Q1756fs*209 Deletion - Frameshift 16:3729780-3729781 - BOR COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - CHC2200T COSM4952925 c.1620G>T p.Q540H Substitution - Missense 16:3781260-3781260 - TCGA-DK-A1AD-01 COSM1301960 c.2080G>C p.V694L Substitution - Missense 16:3778044-3778044 - SC_9047 COSM5563371 c.5723A>G p.Q1908R Substitution - Missense 16:3729324-3729324 - TCGA-85-6561-01 COSM703022 c.1148C>G p.P383R Substitution - Missense 16:3793454-3793454 - ICGC_MB60 COSM3764561 c.3599G>A p.C1200Y Substitution - Missense 16:3757819-3757819 - LP6005334-DNA_E01 COSM4412648 c.1293C>T p.L431L Substitution - coding silent 16:3792018-3792018 - B89-4-Tumor COSM254634 c.3779+1G>T p.? Unknown 16:3751725-3751725 - TCGA-A4-7997-01 COSM3988469 c.3512C>T p.T1171I Substitution - Missense 16:3757906-3757906 - 2492712 COSM5606450 c.3862C>T p.R1288W Substitution - Missense 16:3745329-3745329 - KPOPBR-51-T COSM5964258 c.5205G>A p.T1735T Substitution - coding silent 16:3729842-3729842 - 2492700 COSM5599342 c.7047C>T p.V2349V Substitution - coding silent 16:3728000-3728000 - TCGA-FW-A3R5-06 COSM2919890 c.7112C>T p.P2371L Substitution - Missense 16:3727935-3727935 - S0051 COSM5882714 c.2998G>A p.E1000K Substitution - Missense 16:3769236-3769236 - B62-0-Tumor COSM254630 c.3323C>A p.S1108* Substitution - Nonsense 16:3758900-3758900 - NBL5 COSM1284301 c.4094C>A p.S1365* Substitution - Nonsense 16:3740438-3740438 - B13 COSM254626 c.3874C>T p.Q1292* Substitution - Nonsense 16:3745317-3745317 - TCGA-HC-A6AN-01 COSM970546 c.6310C>T p.R2104C Substitution - Missense 16:3728737-3728737 - TCGA-A6-5665-01 COSM1377817 c.5204C>T p.T1735M Substitution - Missense 16:3729843-3729843 - AOCS-130-1-0 COSM3948543 c.799-10T>A p.? Unknown 16:3810789-3810789 - TCGA-D1-A0ZO-01 COSM970540 c.6871C>A p.L2291M Substitution - Missense 16:3728176-3728176 - CRC-02T COSM2919946 c.4991G>A p.R1664H Substitution - Missense 16:3731373-3731373 - PT33 COSM5909495 c.1655C>T p.P552L Substitution - Missense 16:3781225-3781225 - 2073444 COSM1735705 c.? p.E1035* Substitution - Nonsense FARAGE COSM88733 c.3237G>T p.Q1079H Substitution - Missense 16:3767733-3767733 - pfg020T COSM1640478 c.3305A>G p.Y1102C Substitution - Missense 16:3758918-3758918 - 169 COSM3728526 c.1923C>T p.Y641Y Substitution - coding silent 16:3778718-3778718 - TCGA-HT-8110-01 COSM417011 c.4990C>T p.R1664C Substitution - Missense 16:3731374-3731374 - TCGA-DK-A1A3-01 COSM417010 c.3454C>T p.Q1152* Substitution - Nonsense 16:3757964-3757964 - 112377 COSM95814 c.5475C>G p.L1825L Substitution - coding silent 16:3729572-3729572 - MBRep_T56 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-BR-4361-01 COSM4060712 c.2843A>G p.Q948R Substitution - Missense 16:3770607-3770607 - 1524518 COSM96481 c.?_?del? p.? Unknown S02255 COSM5658750 c.1942-2A>G p.? Unknown 16:3778184-3778184 - 1524432 COSM96455 c.5282C>G p.S1761* Substitution - Nonsense 16:3729765-3729765 - TCGA-AA-A029-01 COSM79348 c.4021C>T p.R1341* Substitution - Nonsense 16:3740511-3740511 - 1536 COSM88773 c.4224delC p.F1410fs*49 Deletion - Frameshift 16:3739634-3739634 - S02294 COSM703032 c.4223G>A p.C1408Y Substitution - Missense 16:3739635-3739635 - TCGA-C8-A26V-01 COSM1478865 c.7115C>T p.S2372L Substitution - Missense 16:3727932-3727932 - FL-PatientA COSM88741 c.4444T>C p.Y1482H Substitution - Missense 16:3736766-3736766 - 1524519 COSM96481 c.?_?del? p.? Unknown 587238 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - S01546 COSM4387385 c.1955A>G p.H652R Substitution - Missense 16:3778169-3778169 - ESCC-F23 COSM5047361 c.6457G>A p.G2153S Substitution - Missense 16:3728590-3728590 - cSCCP8 COSM140751 c.2356C>A p.Q786K Substitution - Missense 16:3773858-3773858 - TCGA-EE-A3J7-06 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 587342 COSM1202273 c.6154C>T p.R2052W Substitution - Missense 16:3728893-3728893 - TCGA-D9-A3Z3-06 COSM3509565 c.1423C>T p.P475S Substitution - Missense 16:3782834-3782834 - TCGA-ED-A5KG-01 COSM4921193 c.3165G>A p.V1055V Substitution - coding silent 16:3767805-3767805 - 2073445 COSM1735705 c.? p.E1035* Substitution - Nonsense FL-PatientA COSM220463 c.3034G>A p.E1012K Substitution - Missense 16:3769200-3769200 - TCGA-AP-A054-01 COSM970564 c.4483A>T p.K1495* Substitution - Nonsense 16:3736727-3736727 - 1524520 COSM96481 c.?_?del? p.? Unknown 193 COSM1741789 c.4094C>G p.S1365* Substitution - Nonsense 16:3740438-3740438 - 1524408 COSM96444 c.5660C>G p.S1887* Substitution - Nonsense 16:3729387-3729387 - TCGA-D1-A17Q-01 COSM970596 c.2294C>A p.S765Y Substitution - Missense 16:3773920-3773920 - TCGA-IR-A3LK-01 COSM4816636 c.386C>T p.S129L Substitution - Missense 16:3850709-3850709 - 16461 COSM5616858 c.6450G>A p.P2150P Substitution - coding silent 16:3728597-3728597 - BD246T COSM5496272 c.1078C>G p.L360V Substitution - Missense 16:3793524-3793524 - LUAD-NYU1210 COSM369651 c.4132C>T p.R1378W Substitution - Missense 16:3740400-3740400 - 587256 COSM1202275 c.5720C>T p.A1907V Substitution - Missense 16:3729327-3729327 - 1649676 COSM166408 c.4471C>A p.Q1491K Substitution - Missense 16:3736739-3736739 - B13-Tumor COSM254626 c.3874C>T p.Q1292* Substitution - Nonsense 16:3745317-3745317 - TCGA-EB-A5UL-06 COSM557988 c.3206G>A p.G1069D Substitution - Missense 16:3767764-3767764 - 1647 COSM88745 c.4508A>T p.Y1503F Substitution - Missense 16:3736702-3736702 - PCSI_0083_Pa_P_526 COSM3787160 c.5024A>G p.H1675R Substitution - Missense 16:3731340-3731340 - 42_tFL COSM4170761 c.2608C>T p.Q870* Substitution - Nonsense 16:3770842-3770842 - 6_tFL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - 587228 COSM1202270 c.5891G>A p.R1964H Substitution - Missense 16:3729156-3729156 - ME100L COSM231338 c.7088C>T p.P2363L Substitution - Missense 16:3727959-3727959 - 851 COSM1159753 c.4991G>T p.R1664L Substitution - Missense 16:3731373-3731373 - NCI-H322M COSM96413 c.2678C>T p.S893L Substitution - Missense 16:3770772-3770772 - SCI-1 COSM88745 c.4508A>T p.Y1503F Substitution - Missense 16:3736702-3736702 - CHC917T COSM3667851 c.6012A>T p.R2004R Substitution - coding silent 16:3729035-3729035 - TCGA-06-0154-01 COSM3402319 c.3575T>C p.V1192A Substitution - Missense 16:3757843-3757843 - TCGA-AP-A0LG-01 COSM970602 c.1937G>A p.S646N Substitution - Missense 16:3778704-3778704 - LIM2405 COSM4613429 c.4268delC p.P1423fs*36 Deletion - Frameshift 16:3739590-3739590 - SC-her2-015 COSM4771563 c.3162_3169delAGTGAAAG p.E1054fs*4 Deletion - Frameshift 16:3767801-3767808 - S02-14875-TP COSM4990884 c.4270C>T p.P1424S Substitution - Missense 16:3739588-3739588 - S0078 COSM5882713 c.3670_3691del22 p.D1224fs*19 Deletion - Frameshift 16:3757295-3757316 - tumor_4144951 COSM5948931 c.4943_4944insC p.I1649fs*11 Insertion - Frameshift 16:3731420-3731421 - PD11177a COSM5945316 c.4246G>T p.E1416* Substitution - Nonsense 16:3739612-3739612 - T231 COSM4674642 c.6325G>A p.V2109M Substitution - Missense 16:3728722-3728722 - 10-P083 COSM4579033 c.113delA p.N38fs*7 Deletion - Frameshift 16:3850982-3850982 - PR-02-2072 COSM243844 c.759C>T p.H253H Substitution - coding silent 16:3850336-3850336 - tumor_4113825 COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - 03-31713 COSM220497 c.4496T>A p.L1499Q Substitution - Missense 16:3736714-3736714 - 745 COSM1159744 c.5038_5039insT p.S1680fs*55 Insertion - Frameshift 16:3731325-3731326 - pfg212T COSM4748954 c.3937A>C p.K1313Q Substitution - Missense 16:3744939-3744939 - TCGA-AP-A059-01 COSM970582 c.3435G>A p.G1145G Substitution - coding silent 16:3757983-3757983 - TCGA-CD-A4MG-01 COSM4060710 c.3836C>T p.P1279L Substitution - Missense 16:3749627-3749627 - SH-0348 COSM5019155 c.5454G>A p.V1818V Substitution - coding silent 16:3729593-3729593 - CSCC-29-T COSM4506277 c.7153C>T p.P2385S Substitution - Missense 16:3727894-3727894 - CHC121T COSM3667852 c.2977C>T p.P993S Substitution - Missense 16:3769257-3769257 - TCGA-AG-3592-01 COSM3420984 c.212C>T p.S71L Substitution - Missense 16:3850883-3850883 - LPJ041 COSM1316076 c.4303G>A p.D1435N Substitution - Missense 16:3738650-3738650 - CSCC-41-T COSM4571305 c.4288T>G p.Y1430D Substitution - Missense 16:3738665-3738665 - TCGA-CZ-5453-01 COSM471710 c.4668A>G p.L1556L Substitution - coding silent 16:3736096-3736096 - TCGA-B8-4621-01 COSM471711 c.977C>T p.S326F Substitution - Missense 16:3793625-3793625 - 215 COSM252982 c.3370-5_3370-4delTT p.? Unknown 16:3758052-3758053 - T3535 COSM3509563 c.2064G>A p.P688P Substitution - coding silent 16:3778060-3778060 - SUP-T1 COSM96468 c.(5830_5832)insC p.?fs Insertion - Frameshift ESCC_51 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-GV-A3JX-01 COSM1301959 c.2666C>G p.S889* Substitution - Nonsense 16:3770784-3770784 - 9T COSM109344 c.1689C>G p.N563K Substitution - Missense 16:3780866-3780866 - B110 COSM88756 c.286C>T p.Q96* Substitution - Nonsense 16:3850809-3850809 - S10-47754-TP COSM4990888 c.2587G>A p.A863T Substitution - Missense 16:3770863-3770863 - TCGA-G4-6311-01 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-29-1703-01 COSM1324454 c.4280+1G>T p.? Unknown 16:3739577-3739577 - S02248 COSM5658241 c.3610-1G>T p.? Unknown 16:3757377-3757377 - TCGA-HU-A4GU-01 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - BN26T COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - CSCC-31-T COSM4502116 c.6052C>T p.P2018S Substitution - Missense 16:3728995-3728995 - TCGA-D1-A177-01 COSM970548 c.6281C>T p.P2094L Substitution - Missense 16:3728766-3728766 - TCGA-B0-5706-01 COSM471712 c.878T>C p.V293A Substitution - Missense 16:3810700-3810700 - 9114_T COSM5041339 c.2068G>C p.A690P Substitution - Missense 16:3778056-3778056 - S00935 COSM5666476 c.4473A>T p.Q1491H Substitution - Missense 16:3736737-3736737 - TCGA-P4-A5EB-01 COSM3988468 c.6030G>A p.G2010G Substitution - coding silent 16:3729017-3729017 - 2126 COSM88738 c.4337G>T p.R1446L Substitution - Missense 16:3738616-3738616 - TCGA-21-1078-01 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - SC_9072 COSM5561772 c.5450C>T p.P1817L Substitution - Missense 16:3729597-3729597 - 2011-2280:2012-366-T COSM4605415 c.4577C>T p.A1526V Substitution - Missense 16:3736187-3736187 - S00935 COSM317184 c.4471_4473delCAA p.Q1491delQ Deletion - In frame 16:3736737-3736739 - SJBALL020994_D1 COSM4989851 c.? p.P1053L Substitution - Missense HN_62506 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - BOR COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - ESCC_BICR_021T COSM5434284 c.4303G>C p.D1435H Substitution - Missense 16:3738650-3738650 - 2206 COSM5012968 c.3828C>A p.D1276E Substitution - Missense 16:3749635-3749635 - PR-00-1165 COSM243843 c.6984G>A p.S2328S Substitution - coding silent 16:3728063-3728063 - T3064 COSM4674648 c.3969A>G p.K1323K Substitution - coding silent 16:3744907-3744907 - 6 COSM88739 c.4349A>G p.Y1450C Substitution - Missense 16:3738604-3738604 - TCGA-CM-6166-01 COSM1377818 c.5064G>A p.T1688T Substitution - coding silent 16:3731300-3731300 - TCGA-FU-A23K-01 COSM460546 c.182C>T p.P61L Substitution - Missense 16:3850913-3850913 - TCGA-D7-6815-01 COSM4060697 c.5451G>A p.P1817P Substitution - coding silent 16:3729596-3729596 - 1649677 COSM88751 c.4448T>G p.I1483S Substitution - Missense 16:3736762-3736762 - GC8_T COSM148008 c.3900C>A p.I1300I Substitution - coding silent 16:3745291-3745291 - CSCC-10-T COSM4542415 c.3183G>A p.E1061E Substitution - coding silent 16:3767787-3767787 - CSCC-56-T COSM4549005 c.4627G>A p.D1543N Substitution - Missense 16:3736137-3736137 - 671204 COSM1644510 c.1187C>G p.T396R Substitution - Missense 16:3793415-3793415 - Patient_3_Relapse COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-AD-6964-01 COSM2920000 c.3250_3250+1insA p.I1084fs*3 Unknown 16:3767719-3767720 - CSCC-29-T COSM4567442 c.7154_7155CC>TA p.P2385L Substitution - Missense 16:3727892-3727893 - BCM325T COSM4798976 c.4213G>C p.V1405L Substitution - Missense 16:3739645-3739645 - KM12 COSM417011 c.4990C>T p.R1664C Substitution - Missense 16:3731374-3731374 - PTC-7C COSM4129054 c.2604T>A p.S868S Substitution - coding silent 16:3770846-3770846 - 40M COSM5584914 c.2488C>T p.P830S Substitution - Missense 16:3770962-3770962 - TCGA-BR-8368-01 COSM4060702 c.4948G>A p.V1650I Substitution - Missense 16:3731416-3731416 - BL42 COSM3728000 c.4263_4264insC p.P1424fs*13 Insertion - Frameshift 16:3739594-3739595 - DM34 COSM5608143 c.4732A>T p.S1578C Substitution - Missense 16:3731934-3731934 - J65_T COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - LUAD_E00522 COSM352596 c.4648G>C p.E1550Q Substitution - Missense 16:3736116-3736116 - UD-SCC-2 COSM4260243 c.4471C>G p.Q1491E Substitution - Missense 16:3736739-3736739 - ESCC-139T COSM96444 c.5660C>G p.S1887* Substitution - Nonsense 16:3729387-3729387 - 2209 COSM88755 c.223C>T p.R75* Substitution - Nonsense 16:3850872-3850872 - TCGA-DJ-A2Q8-01 COSM3370431 c.2018T>A p.L673* Substitution - Nonsense 16:3778106-3778106 - 2170 COSM88770 c.3301_3302ins41 p.L1101fs*12 Insertion - Frameshift 16:3758921-3758922 - 3_tFL COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - Pat_16_A COSM5850893 c.2930C>T p.S977L Substitution - Missense 16:3769304-3769304 - T164 COSM307690 c.3779+1delG p.? Unknown 16:3751725-3751725 - TCGA-BR-6452-01 COSM4060719 c.1170C>T p.N390N Substitution - coding silent 16:3793432-3793432 - B110 COSM88756 c.286C>T p.Q96* Substitution - Nonsense 16:3850809-3850809 - TCGA-EE-A182-06 COSM3509554 c.4432G>A p.E1478K Substitution - Missense 16:3736778-3736778 - TCGA-BS-A0UA-01 COSM970548 c.6281C>T p.P2094L Substitution - Missense 16:3728766-3728766 - 8062308 COSM84329 c.6841G>A p.A2281T Substitution - Missense 16:3728206-3728206 - LUAD-RT-S01702 COSM379083 c.1133G>A p.R378Q Substitution - Missense 16:3793469-3793469 - 587238 COSM1202269 c.6596A>T p.Q2199L Substitution - Missense 16:3728451-3728451 - 1524371 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - FL17 COSM88765 c.3702T>G p.Y1234* Substitution - Nonsense 16:3751803-3751803 - QC2-05-T2 COSM5656383 c.3233_3250+30del48 p.? Unknown 16:3767690-3767737 - B37-Tumor COSM254627 c.310C>T p.Q104* Substitution - Nonsense 16:3850785-3850785 - pfg043T COSM4748955 c.3722T>A p.F1241Y Substitution - Missense 16:3751783-3751783 - Pat_76_A COSM5850895 c.2296_2297CC>TT p.P766F Substitution - Missense 16:3773917-3773918 - 04-39108 COSM220498 c.4463C>G p.P1488R Substitution - Missense 16:3736747-3736747 - TCGA-BT-A20O-01 COSM417009 c.3221C>G p.S1074* Substitution - Nonsense 16:3767749-3767749 - SH-1641 COSM5019178 c.7212A>G p.E2404E Substitution - coding silent 16:3727835-3727835 - 587224 COSM970546 c.6310C>T p.R2104C Substitution - Missense 16:3728737-3728737 - TCGA-D5-6920-01 COSM1377844 c.3507C>T p.R1169R Substitution - coding silent 16:3757911-3757911 - PD6486a COSM4384868 c.5234G>A p.W1745* Substitution - Nonsense 16:3729813-3729813 - B63 COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - ICGC_MB68 COSM88738 c.4337G>T p.R1446L Substitution - Missense 16:3738616-3738616 - LUAD-CHTN-Z4716A COSM361828 c.4198G>T p.E1400* Substitution - Nonsense 16:3739660-3739660 - SUDHL8 COSM88775 c.1573+2T>C p.? Unknown 16:3782682-3782682 - 2101 COSM96481 c.?_?del? p.? Unknown CAL27 COSM2919889 c.7169C>A p.T2390N Substitution - Missense 16:3727878-3727878 - TCGA-DD-A1EA-01 COSM4920089 c.6428A>G p.N2143S Substitution - Missense 16:3728619-3728619 - I2L-P19Ta-Tumor-Biopsy COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - B59 COSM254629 c.3217C>T p.Q1073* Substitution - Nonsense 16:3767753-3767753 - LC_S3 COSM1189167 c.2965G>T p.G989* Substitution - Nonsense 16:3769269-3769269 - CSCC-40-T COSM1734409 c.2925delC p.S976fs*22 Deletion - Frameshift 16:3769309-3769309 - TCGA-21-1081-01 COSM703029 c.2827C>T p.Q943* Substitution - Nonsense 16:3770623-3770623 - Karpas422 COSM220975 c.3712G>T p.E1238* Substitution - Nonsense 16:3751793-3751793 - 004 COSM4169377 c.4404_4405delAG p.G1469fs*9 Deletion - Frameshift 16:3736805-3736806 - HCC40T COSM166411 c.3836+1G>A p.? Unknown 16:3749626-3749626 - S00501 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - 2334199 COSM319672 c.4395-1G>A p.? Unknown 16:3736816-3736816 - Pat_59_A COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - RK148_C01 COSM1629891 c.576C>G p.N192K Substitution - Missense 16:3850519-3850519 - GLC2 COSM318345 c.5140G>T p.V1714L Substitution - Missense 16:3731224-3731224 - 2040 COSM88735 c.3959A>G p.K1320R Substitution - Missense 16:3744917-3744917 - ESOSCC164T COSM1172330 c.4807G>T p.A1603S Substitution - Missense 16:3731859-3731859 - 4 COSM88739 c.4349A>G p.Y1450C Substitution - Missense 16:3738604-3738604 - ov519A COSM96412 c.1399G>A p.A467T Substitution - Missense 16:3782858-3782858 - S00538 COSM318346 c.4179C>G p.T1393T Substitution - coding silent 16:3739679-3739679 - PD5937a COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - TCGA-C8-A1HE-01 COSM1478868 c.3271C>T p.R1091C Substitution - Missense 16:3758952-3758952 - SC-her2-046 COSM4943266 c.5732C>T p.P1911L Substitution - Missense 16:3729315-3729315 - 6115115 COSM5384870 c.2961G>A p.Q987Q Substitution - coding silent 16:3769273-3769273 - H9 COSM5878670 c.6087G>T p.Q2029H Substitution - Missense 16:3728960-3728960 - TCGA-AA-3672-01 COSM266307 c.6215G>A p.R2072Q Substitution - Missense 16:3728832-3728832 - TCGA-AP-A059-01 COSM970594 c.2573C>T p.P858L Substitution - Missense 16:3770877-3770877 - TCGA-EE-A2GP-06 COSM3509556 c.3884T>C p.V1295A Substitution - Missense 16:3745307-3745307 - B5-Tumor COSM254628 c.1063C>T p.Q355* Substitution - Nonsense 16:3793539-3793539 - tumor_4149246 COSM166409 c.4448T>C p.I1483T Substitution - Missense 16:3736762-3736762 - TCGA-BR-8487-01 COSM4060696 c.6214C>T p.R2072W Substitution - Missense 16:3728833-3728833 - TCGA-EE-A2MD-06 COSM1726101 c.5399G>A p.R1800Q Substitution - Missense 16:3729648-3729648 - TCGA-EI-6507-01 COSM1563118 c.3775C>T p.Q1259* Substitution - Nonsense 16:3751730-3751730 - Au2 COSM5599342 c.7047C>T p.V2349V Substitution - coding silent 16:3728000-3728000 - S01020 COSM5701405 c.1108_1109insT p.R370fs*57 Insertion - Frameshift 16:3793493-3793494 - TCGA-BR-8680-01 COSM970612 c.775G>A p.A259T Substitution - Missense 16:3850320-3850320 - TCGA-EP-A2KA-01 COSM4917655 c.6657C>A p.A2219A Substitution - coding silent 16:3728390-3728390 - 2040 COSM88761 c.3967A>T p.K1323* Substitution - Nonsense 16:3744909-3744909 - CN-AML-NR-08-Dx COSM148010 c.2784G>A p.P928P Substitution - coding silent 16:3770666-3770666 - S01023 COSM318347 c.4232G>T p.G1411V Substitution - Missense 16:3739626-3739626 - 42 COSM5762854 c.2728A>G p.T910A Substitution - Missense 16:3770722-3770722 - PD8138a COSM5945318 c.2283+1G>A p.? Unknown 16:3774568-3774568 - PD9694a COSM703029 c.2827C>T p.Q943* Substitution - Nonsense 16:3770623-3770623 - T3182 COSM4674643 c.6324C>T p.Y2108Y Substitution - coding silent 16:3728723-3728723 - TCGA-ER-A3PL-06 COSM3509564 c.1846C>T p.P616S Substitution - Missense 16:3778795-3778795 - TCGA-AP-A0LP-01 COSM970534 c.7192G>T p.G2398* Substitution - Nonsense 16:3727855-3727855 - HCC49T COSM1609324 c.234C>T p.S78S Substitution - coding silent 16:3850861-3850861 - tumor_4108992 COSM220497 c.4496T>A p.L1499Q Substitution - Missense 16:3736714-3736714 - pfg081T COSM88756 c.286C>T p.Q96* Substitution - Nonsense 16:3850809-3850809 - TCGA-BS-A0TC-01 COSM970568 c.4317C>A p.F1439L Substitution - Missense 16:3738636-3738636 - CSCC-20-T COSM4504844 c.6764C>T p.P2255L Substitution - Missense 16:3728283-3728283 - ESCC-F68 COSM5048309 c.1074_1075insAG p.V359fs*31 Insertion - Frameshift 16:3793527-3793528 - LPJ103 COSM88737 c.4305T>A p.D1435E Substitution - Missense 16:3738648-3738648 - 3N54-VS-3T54 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - MOLT-4 COSM1678810 c.1171G>A p.V391I Substitution - Missense 16:3793431-3793431 - 00-15694 COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - SC_9017 COSM5561951 c.7149C>T p.P2383P Substitution - coding silent 16:3727898-3727898 - TCGA-A5-A0GA-01 COSM970610 c.1103_1104insA p.R369fs*58 Insertion - Frameshift 16:3793498-3793499 - ESO-1481 COSM1249110 c.6452G>A p.R2151Q Substitution - Missense 16:3728595-3728595 - CHC1744T COSM4792357 c.3719G>A p.C1240Y Substitution - Missense 16:3751786-3751786 - ESCC_162 COSM5647832 c.3172G>C p.E1058Q Substitution - Missense 16:3767798-3767798 - S02400 COSM5699767 c.2004delA p.K668fs*27 Deletion - Frameshift 16:3778120-3778120 - GHE1437 COSM5715141 c.3034G>T p.E1012* Substitution - Nonsense 16:3769200-3769200 - NU-DHL-1 COSM220976 c.1307C>T p.A436V Substitution - Missense 16:3792004-3792004 - 6T COSM3734328 c.6484G>C p.G2162R Substitution - Missense 16:3728563-3728563 - PD6780a COSM4384875 c.328G>T p.A110S Substitution - Missense 16:3850767-3850767 - Pat_05_A COSM5850892 c.3023_3024CC>TT p.P1008L Substitution - Missense 16:3769210-3769211 - PD6824a COSM4384866 c.5621C>T p.T1874I Substitution - Missense 16:3729426-3729426 - CSCC-49-T COSM4469317 c.1594C>T p.P532S Substitution - Missense 16:3781286-3781286 - 10-P1058 COSM4579029 c.6933G>A p.P2311P Substitution - coding silent 16:3728114-3728114 - TCGA-BR-4256-01 COSM88763 c.4078C>T p.R1360* Substitution - Nonsense 16:3740454-3740454 - B89-4-Tumor COSM254635 c.1258A>T p.K420* Substitution - Nonsense 16:3792053-3792053 - I2L-P7-Tumor-Organoid COSM5363737 c.556C>T p.P186S Substitution - Missense 16:3850539-3850539 - TCGA-G7-A4TM-01 COSM3988471 c.942C>T p.I314I Substitution - coding silent 16:3810636-3810636 - MKB-1 COSM96472 c.2064delG p.A690fs*5 Deletion - Frameshift 16:3778060-3778060 - ICGC_MB56 COSM166408 c.4471C>A p.Q1491K Substitution - Missense 16:3736739-3736739 - TCGA-AP-A059-01 COSM970538 c.6949C>A p.Q2317K Substitution - Missense 16:3728098-3728098 - Pat_14_A COSM5850889 c.7150C>A p.H2384N Substitution - Missense 16:3727897-3727897 - 2011-2269:2012-1328-T COSM4605184 c.3483C>T p.F1161F Substitution - coding silent 16:3757935-3757935 - TCGA-FP-A4BE-01 COSM172758 c.7030C>T p.R2344W Substitution - Missense 16:3728017-3728017 - TCGA-AP-A059-01 COSM970614 c.732G>A p.T244T Substitution - coding silent 16:3850363-3850363 - B89-4 COSM254635 c.1258A>T p.K420* Substitution - Nonsense 16:3792053-3792053 - tumor_4111326 COSM88743 c.4507T>G p.Y1503D Substitution - Missense 16:3736703-3736703 - TCGA-BR-7851-01 COSM4060707 c.4556A>G p.Y1519C Substitution - Missense 16:3736654-3736654 - 1524517 COSM96453 c.? p.C1408Y Substitution - Missense C086 COSM5529207 c.2099C>T p.P700L Substitution - Missense 16:3778025-3778025 - 2108 COSM88732 c.3158C>T p.P1053L Substitution - Missense 16:3767812-3767812 - GC8_T COSM148009 c.3837-8C>T p.? Unknown 16:3745362-3745362 - B89-1 COSM255051 c.1890_1893delAGCC p.A631fs*23 Deletion - Frameshift 16:3778748-3778751 - S03-45671-TP COSM88759 c.2254C>T p.Q752* Substitution - Nonsense 16:3774598-3774598 - S12-22512-TP COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - S01023 COSM318347 c.4232G>T p.G1411V Substitution - Missense 16:3739626-3739626 - TCGA-FS-A1ZK-06 COSM3509548 c.7086C>T p.S2362S Substitution - coding silent 16:3727961-3727961 - TCGA-F5-6814-01 COSM3420983 c.910G>A p.V304I Substitution - Missense 16:3810668-3810668 - TCGA-06-0749-01 COSM2151925 c.1256G>A p.W419* Substitution - Nonsense 16:3792055-3792055 - ccRCC-18 COSM1659201 c.2159-9C>T p.? Unknown 16:3774702-3774702 - CHC2200T COSM4952925 c.1620G>T p.Q540H Substitution - Missense 16:3781260-3781260 - Pat_41_B COSM5850896 c.1022C>T p.A341V Substitution - Missense 16:3793580-3793580 - ICGC_MB82 COSM3764560 c.4447A>T p.I1483F Substitution - Missense 16:3736763-3736763 - TCGA-BR-8363-01 COSM4060709 c.4212C>T p.G1404G Substitution - coding silent 16:3739646-3739646 - 1524436 COSM96451 c.? p.P688A Substitution - Missense 08-11596 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 1524429 COSM96481 c.?_?del? p.? Unknown FL28 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - LUAD-RT-S01702 COSM379084 c.913A>G p.N305D Substitution - Missense 16:3810665-3810665 - I2L-P19Tb-Tumor-Biopsy COSM2919923 c.5552G>A p.R1851H Substitution - Missense 16:3729495-3729495 - PD8939a COSM4384874 c.485C>T p.A162V Substitution - Missense 16:3850610-3850610 - TCGA-BR-A4QL-01 COSM3937064 c.1873C>T p.R625C Substitution - Missense 16:3778768-3778768 - 1524427 COSM96448 c.? p.P858S Substitution - Missense TCGA-AX-A0J0-01 COSM970606 c.1612A>C p.T538P Substitution - Missense 16:3781268-3781268 - SJMB129 COSM255286 c.1621C>T p.Q541* Substitution - Nonsense 16:3781259-3781259 - OCI-Ly8 COSM88734 c.3718T>C p.C1240R Substitution - Missense 16:3751787-3751787 - TCGA-BS-A0TA-01 COSM970536 c.7089G>A p.P2363P Substitution - coding silent 16:3727958-3727958 - CSCC-47-T COSM4482913 c.2651C>T p.A884V Substitution - Missense 16:3770799-3770799 - CSCC-15-T COSM4495171 c.4480C>A p.P1494T Substitution - Missense 16:3736730-3736730 - SH-5693 COSM5020442 c.4280+8T>C p.? Unknown 16:3739570-3739570 - 1115183 COSM5556130 c.2688G>A p.G896G Substitution - coding silent 16:3770762-3770762 - ESCC_149 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - tumor_4177987 COSM3356828 c.4463C>T p.P1488L Substitution - Missense 16:3736747-3736747 - 101286 COSM95815 c.4860G>A p.K1620K Substitution - coding silent 16:3731806-3731806 - 23_tFL COSM4170753 c.4501_4503delGAG p.E1501delE Deletion - In frame 16:3736707-3736709 - TCGA-43-5668-01 COSM703021 c.682A>G p.T228A Substitution - Missense 16:3850413-3850413 - CHC2351T COSM4801224 c.681T>A p.P227P Substitution - coding silent 16:3850414-3850414 - 2321334 COSM4775059 c.5371T>C p.S1791P Substitution - Missense 16:3729676-3729676 - EGC15 COSM5054884 c.4340C>T p.T1447I Substitution - Missense 16:3738613-3738613 - TCGA-AN-A0AT-01 COSM435238 c.2390_2391insA p.N797fs*35 Insertion - Frameshift 16:3773823-3773824 - HCT15 COSM1678808 c.3449C>A p.P1150H Substitution - Missense 16:3757969-3757969 - TCGA-C4-A0F0-01 COSM220496 c.4307G>A p.S1436N Substitution - Missense 16:3738646-3738646 - PD6063a COSM4384870 c.3829C>G p.P1277A Substitution - Missense 16:3749634-3749634 - B89-1 COSM255051 c.1890_1893delAGCC p.A631fs*23 Deletion - Frameshift 16:3778748-3778751 - MKB-1 COSM96460 c.760G>A p.A254T Substitution - Missense 16:3850335-3850335 - 29_tFL COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - 29_FL COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - TCGA-D1-A16D-01 COSM970570 c.4311T>G p.I1437M Substitution - Missense 16:3738642-3738642 - FL8 COSM88750 c.4301T>C p.L1434P Substitution - Missense 16:3738652-3738652 - 1524435 COSM96451 c.? p.P688A Substitution - Missense UD-SCC-2 COSM4260242 c.4548C>G p.I1516M Substitution - Missense 16:3736662-3736662 - 1524430 COSM96481 c.?_?del? p.? Unknown 2020 COSM79348 c.4021C>T p.R1341* Substitution - Nonsense 16:3740511-3740511 - TCGA-33-4532-01 COSM703034 c.4348T>G p.Y1450D Substitution - Missense 16:3738605-3738605 - OV207 COSM252982 c.3370-5_3370-4delTT p.? Unknown 16:3758052-3758053 - PD8289a COSM4384868 c.5234G>A p.W1745* Substitution - Nonsense 16:3729813-3729813 - CSCC-56-T COSM4455041 c.6476A>T p.Q2159L Substitution - Missense 16:3728571-3728571 - PT48 COSM4990893 c.598C>T p.Q200* Substitution - Nonsense 16:3850497-3850497 - TL79 COSM5752051 c.5848C>CT p.Q1950fs*16 Complex - frameshift 16:3729199-3729199 - Sample_1 COSM4997568 c.5635C>A p.Q1879K Substitution - Missense 16:3729412-3729412 - TCGA-G3-A25S-01 COSM4926947 c.3778A>G p.T1260A Substitution - Missense 16:3751727-3751727 - 223 COSM4425425 c.1644A>G p.E548E Substitution - coding silent 16:3781236-3781236 - PD6083a COSM4384863 c.6910C>T p.Q2304* Substitution - Nonsense 16:3728137-3728137 - ICGC_MB82 COSM3764560 c.4447A>T p.I1483F Substitution - Missense 16:3736763-3736763 - TCGA-G4-6628-01 COSM1377857 c.1942-1G>T p.? Unknown 16:3778183-3778183 - 1373570 COSM5702561 c.4561-1G>A p.? Unknown 16:3736204-3736204 - SH-1439 COSM5019155 c.5454G>A p.V1818V Substitution - coding silent 16:3729593-3729593 - HCT8 COSM4634083 c.5813C>A p.P1938H Substitution - Missense 16:3729234-3729234 - TCGA-HE-A5NJ-01 COSM4414487 c.95C>T p.S32L Substitution - Missense 16:3851000-3851000 - TCGA-29-1699-01 COSM1324451 c.858G>T p.Q286H Substitution - Missense 16:3810720-3810720 - T96 COSM4674654 c.2012C>T p.S671L Substitution - Missense 16:3778112-3778112 - TCGA-P4-A5EA-01 COSM3988470 c.3148G>T p.E1050* Substitution - Nonsense 16:3767822-3767822 - CP66-MEL COSM21712 c.2809C>T p.P937S Substitution - Missense 16:3770641-3770641 - 260211 COSM3726026 c.1521G>T p.Q507H Substitution - Missense 16:3782736-3782736 - TCGA-AP-A059-01 COSM970544 c.6424C>A p.L2142M Substitution - Missense 16:3728623-3728623 - 41T COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - B98-Tumor COSM1756924 c.6513G>A p.L2171L Substitution - coding silent 16:3728534-3728534 - TCGA-D1-A103-01 COSM970560 c.4901T>C p.V1634A Substitution - Missense 16:3731463-3731463 - PDA_100 COSM5003455 c.2900G>A p.S967N Substitution - Missense 16:3769334-3769334 - STC246 COSM5054883 c.4424C>G p.P1475R Substitution - Missense 16:3736786-3736786 - tumor_4111326 COSM5949992 c.1792C>T p.Q598* Substitution - Nonsense 16:3780763-3780763 - QC2-35-T2 COSM5656319 c.5034_5036delCTC p.S1680delS Deletion - In frame 16:3731328-3731330 - 1649664 COSM166410 c.1744_1745CC>TTT p.P582fs*4 Complex - frameshift 16:3780810-3780811 - CHOL09 COSM1744876 c.2498_2499delTC p.L833fs*136 Deletion - Frameshift 16:3770951-3770952 - C709 COSM4443886 c.5944C>T p.P1982S Substitution - Missense 16:3729103-3729103 - 464 COSM1159754 c.4492C>T p.R1498* Substitution - Nonsense 16:3736718-3736718 - TCGA-39-5031-01 COSM703037 c.5300C>T p.S1767L Substitution - Missense 16:3729747-3729747 - TCGA-C8-A26Y-01 COSM3817966 c.360G>A p.K120K Substitution - coding silent 16:3850735-3850735 - CSCC-62-T COSM4481984 c.2562C>T p.H854H Substitution - coding silent 16:3770888-3770888 - HCC40 COSM166411 c.3836+1G>A p.? Unknown 16:3749626-3749626 - B5 COSM254628 c.1063C>T p.Q355* Substitution - Nonsense 16:3793539-3793539 - TCGA-AP-A0LM-01 COSM970584 c.3321G>A p.E1107E Substitution - coding silent 16:3758902-3758902 - pfg068T COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - 3492 COSM1644509 c.4358T>A p.I1453N Substitution - Missense 16:3738595-3738595 - TCGA-ER-A19P-06 COSM3509567 c.1201G>T p.G401W Substitution - Missense 16:3793401-3793401 - TCGA-AM-5820-01 COSM3690998 c.1229C>T p.A410V Substitution - Missense 16:3792082-3792082 - TCGA-14-1453 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - LUAD-D01603 COSM337449 c.3147T>C p.D1049D Substitution - coding silent 16:3767823-3767823 - 1649665 COSM166410 c.1744_1745CC>TTT p.P582fs*4 Complex - frameshift 16:3780810-3780811 - I2L-P9-Tumor-Organoid COSM1249109 c.4209C>T p.D1403D Substitution - coding silent 16:3739649-3739649 - CSCC-31-T COSM2919906 c.6227C>T p.S2076L Substitution - Missense 16:3728820-3728820 - TCGA-EA-A1QT-01 COSM460549 c.4627G>C p.D1543H Substitution - Missense 16:3736137-3736137 - PT55 COSM5942649 c.3329C>T p.P1110L Substitution - Missense 16:3758894-3758894 - BT0167 COSM96413 c.2678C>T p.S893L Substitution - Missense 16:3770772-3770772 - T3094 COSM4674649 c.3605G>A p.R1202H Substitution - Missense 16:3757813-3757813 - B109-Tumor COSM254625 c.4336C>G p.R1446G Substitution - Missense 16:3738617-3738617 - B63-Tumor COSM88753 c.4506G>T p.W1502C Substitution - Missense 16:3736704-3736704 - BZ33 COSM5760507 c.4646T>A p.L1549* Substitution - Nonsense 16:3736118-3736118 - DM59 COSM3420981 c.3832G>A p.E1278K Substitution - Missense 16:3749631-3749631 - TCGA-EI-6917-01 COSM3420981 c.3832G>A p.E1278K Substitution - Missense 16:3749631-3749631 - SH-9248 COSM5019155 c.5454G>A p.V1818V Substitution - coding silent 16:3729593-3729593 - 2492721 COSM5724226 c.2867C>T p.P956L Substitution - Missense 16:3770583-3770583 - S01-27743-TP COSM352596 c.4648G>C p.E1550Q Substitution - Missense 16:3736116-3736116 - CSCC-20-T COSM4491149 c.3759C>T p.D1253D Substitution - coding silent 16:3751746-3751746 - ACINAR03 COSM1734409 c.2925delC p.S976fs*22 Deletion - Frameshift 16:3769309-3769309 - WSU-HN6 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - 1N04-VS-1T04 COSM4972772 c.1095delT p.H365fs*24 Deletion - Frameshift 16:3793507-3793507 - 6_FL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - J30_T COSM3957566 c.3527A>T p.K1176M Substitution - Missense 16:3757891-3757891 - TCGA-BR-6566-01 COSM4060711 c.3415A>G p.K1139E Substitution - Missense 16:3758003-3758003 - PT23_2 COSM88741 c.4444T>C p.Y1482H Substitution - Missense 16:3736766-3736766 - NU-DHL-1 COSM220977 c.508C>T p.Q170* Substitution - Nonsense 16:3850587-3850587 - TCGA-HC-7077-01 COSM3672255 c.4148G>T p.G1383V Substitution - Missense 16:3739710-3739710 - HCC70T COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 587222 COSM1202271 c.2224C>T p.R742C Substitution - Missense 16:3774628-3774628 - TCGA-D3-A3MR-06 COSM3509551 c.6311G>C p.R2104P Substitution - Missense 16:3728736-3728736 - NCI-H2122 COSM21711 c.248A>C p.N83T Substitution - Missense 16:3850847-3850847 - NCI-H2122 COSM21711 c.248A>C p.N83T Substitution - Missense 16:3850847-3850847 - CSCC-55-T COSM2920015 c.2640C>T p.P880P Substitution - coding silent 16:3770810-3770810 - TCGA-D3-A51T-06 COSM3509566 c.1246A>G p.I416V Substitution - Missense 16:3792065-3792065 - TCGA-EE-A2M5-06 COSM3509569 c.569A>T p.N190I Substitution - Missense 16:3850526-3850526 - OCI-Ly1 COSM88768 c.1718delC p.L574fs*15 Deletion - Frameshift 16:3780837-3780837 - TCGA-BR-7851-01 COSM4060690 c.7161C>T p.L2387L Substitution - coding silent 16:3727886-3727886 - C086 COSM5529208 c.2922C>T p.T974T Substitution - coding silent 16:3769312-3769312 - ESCC_BICR_055T COSM148008 c.3900C>A p.I1300I Substitution - coding silent 16:3745291-3745291 - Jurkat COSM96464 c.4071delT p.F1358fs*18 Deletion - Frameshift 16:3740461-3740461 - MT-260-T2 COSM5656359 c.3874_3875insA p.I1293fs*7 Insertion - Frameshift 16:3745316-3745317 - 1649667 COSM166405 c.4232G>A p.G1411E Substitution - Missense 16:3739626-3739626 - 2161 COSM88757 c.466C>T p.Q156* Substitution - Nonsense 16:3850629-3850629 - ov623 COSM96417 c.567delC p.N190fs*8 Deletion - Frameshift 16:3850528-3850528 - TCGA-D3-A2J7-06 COSM3509557 c.3329C>G p.P1110R Substitution - Missense 16:3758894-3758894 - HCC2998 COSM4631608 c.5719G>A p.A1907T Substitution - Missense 16:3729328-3729328 - ML-2 COSM96465 c.3269T>A p.L1090* Substitution - Nonsense 16:3758954-3758954 - TARGET-20-PARCVS-04A-01D COSM5487609 c.1760_1761insG p.V588fs*20 Insertion - Frameshift 16:3780794-3780795 - B66 COSM254631 c.6983C>T p.S2328L Substitution - Missense 16:3728064-3728064 - 041T COSM1729096 c.331A>T p.N111Y Substitution - Missense 16:3850764-3850764 - 44_T COSM3957564 c.5048G>C p.R1683P Substitution - Missense 16:3731316-3731316 - 2492723 COSM5724226 c.2867C>T p.P956L Substitution - Missense 16:3770583-3770583 - TCGA-18-3411-01 COSM703020 c.170G>T p.G57V Substitution - Missense 16:3850925-3850925 - TCGA-EE-A2GC-06 COSM3509561 c.2236C>T p.P746S Substitution - Missense 16:3774616-3774616 - SUDHL6 COSM88767 c.1407delT p.L470fs*1 Deletion - Frameshift 16:3782850-3782850 - TCGA-C5-A1BJ-01 COSM4830676 c.674C>T p.P225L Substitution - Missense 16:3850421-3850421 - S02-14875-TP COSM4990883 c.4271C>T p.P1424L Substitution - Missense 16:3739587-3739587 - PD11131a COSM5945315 c.5284A>T p.K1762* Substitution - Nonsense 16:3729763-3729763 - 8165 COSM5751432 c.1108C>CT p.R370fs*57 Complex - frameshift 16:3793494-3793494 - SUDHL7 COSM88739 c.4349A>G p.Y1450C Substitution - Missense 16:3738604-3738604 - TCGA-DD-A3A8-01 COSM4934881 c.3695A>G p.N1232S Substitution - Missense 16:3757291-3757291 - 2012-693:2012-1306-T COSM4604059 c.1100G>T p.C367F Substitution - Missense 16:3793502-3793502 - TCGA-BR-7851-01 COSM3817961 c.5063C>T p.T1688M Substitution - Missense 16:3731301-3731301 - 24_tFL COSM4170757 c.4307G>T p.S1436I Substitution - Missense 16:3738646-3738646 - OSCC-GB_00880111 COSM4888087 c.5440G>A p.G1814R Substitution - Missense 16:3729607-3729607 - IGROV-1 COSM1678807 c.3478A>G p.M1160V Substitution - Missense 16:3757940-3757940 - 1524438 COSM96452 c.? p.G1069S Substitution - Missense T1194 COSM4674652 c.2667_2669delAAC p.T890delT Deletion - In frame 16:3770781-3770783 - OVCAR-5 COSM96416 c.3211G>A p.A1071T Substitution - Missense 16:3767759-3767759 - CH-60-T2 COSM5651303 c.3091C>T p.Q1031* Substitution - Nonsense 16:3767879-3767879 - 6P2-2 COSM3734328 c.6484G>C p.G2162R Substitution - Missense 16:3728563-3728563 - PD11234a COSM5945317 c.2318C>T p.P773L Substitution - Missense 16:3773896-3773896 - PTC-7C COSM4129055 c.2598G>T p.M866I Substitution - Missense 16:3770852-3770852 - P0041 COSM5885284 c.? p.A138D Substitution - Missense S09-31237-TP COSM4990890 c.1614A>G p.T538T Substitution - coding silent 16:3781266-3781266 - SH-0348 COSM5019178 c.7212A>G p.E2404E Substitution - coding silent 16:3727835-3727835 - TCGA-G4-6628-01 COSM1377839 c.3882C>T p.C1294C Substitution - coding silent 16:3745309-3745309 - LPJ023 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - PT19_1 COSM252981 c.3370-4delT p.? Unknown 16:3758052-3758052 - C135 COSM4610998 c.4680_4682delAGA p.E1562delE Deletion - In frame 16:3736082-3736084 - TCGA-AN-A046-01 COSM1377845 c.3505C>T p.R1169C Substitution - Missense 16:3757913-3757913 - TCGA-EE-A3JD-06 COSM4396124 c.798G>A p.K266K Substitution - coding silent 16:3850297-3850297 - TCGA-CD-A4MG-01 COSM4060713 c.2506C>A p.L836M Substitution - Missense 16:3770944-3770944 - TCGA-B5-A0JS-01 COSM970608 c.1585A>G p.M529V Substitution - Missense 16:3781295-3781295 - 08-P054 COSM4579031 c.5439C>T p.N1813N Substitution - coding silent 16:3729608-3729608 - REX COSM96463 c.3246delA p.I1084fs*15 Deletion - Frameshift 16:3767724-3767724 - H322T COSM96413 c.2678C>T p.S893L Substitution - Missense 16:3770772-3770772 - 32 COSM96413 c.2678C>T p.S893L Substitution - Missense 16:3770772-3770772 - ESCC_160 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - 2109 COSM88746 c.5035_5037delTCC p.S1680delS Deletion - In frame 16:3731327-3731329 - PD4132a COSM160204 c.4686G>A p.E1562E Substitution - coding silent 16:3736078-3736078 - CSCC-11-T COSM4466263 c.1424C>T p.P475L Substitution - Missense 16:3782833-3782833 - PT24_2 COSM5904632 c.4424C>T p.P1475L Substitution - Missense 16:3736786-3736786 - S06-38853-TP COSM4990885 c.3396C>T p.P1132P Substitution - coding silent 16:3758022-3758022 - TCGA-FW-A3R5-06 COSM3888515 c.3840C>T p.F1280F Substitution - coding silent 16:3745351-3745351 - TCGA-F4-6808-01 COSM3690997 c.5356C>T p.R1786C Substitution - Missense 16:3729691-3729691 - TCGA-J9-A52C-01 COSM4877446 c.5147C>T p.T1716M Substitution - Missense 16:3731217-3731217 - UPCI:SCC090 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - PD10941a COSM5945314 c.5566C>T p.Q1856* Substitution - Nonsense 16:3729481-3729481 - 1649683 COSM88747 c.4304A>G p.D1435G Substitution - Missense 16:3738649-3738649 - pfg103T COSM4748966 c.761C>T p.A254V Substitution - Missense 16:3850334-3850334 - BCM325T COSM4798976 c.4213G>C p.V1405L Substitution - Missense 16:3739645-3739645 - DM18 COSM5608140 c.823C>T p.P275S Substitution - Missense 16:3810755-3810755 - T3225 COSM4674657 c.536C>T p.A179V Substitution - Missense 16:3850559-3850559 - PD6165a COSM4384872 c.1594C>A p.P532T Substitution - Missense 16:3781286-3781286 - QC2-04-T2 COSM5651884 c.4463C>A p.P1488Q Substitution - Missense 16:3736747-3736747 - 43_tFL COSM3356828 c.4463C>T p.P1488L Substitution - Missense 16:3736747-3736747 - BZ34 COSM5760508 c.6604C>T p.Q2202* Substitution - Nonsense 16:3728443-3728443 - HN_62814 COSM122355 c.2849C>T p.T950M Substitution - Missense 16:3770601-3770601 - 1649671 COSM166411 c.3836+1G>A p.? Unknown 16:3749626-3749626 - SK00102_P COSM79348 c.4021C>T p.R1341* Substitution - Nonsense 16:3740511-3740511 - TCGA-AA-A010-01 COSM280131 c.270C>T p.S90S Substitution - coding silent 16:3850825-3850825 - TCGA-BH-A0W7-01 COSM435236 c.6303C>G p.I2101M Substitution - Missense 16:3728744-3728744 - B59-Tumor COSM254629 c.3217C>T p.Q1073* Substitution - Nonsense 16:3767753-3767753 - CAL33 COSM4593308 c.6682C>G p.H2228D Substitution - Missense 16:3728365-3728365 - Gp2D COSM4627414 c.1053C>T p.R351R Substitution - coding silent 16:3793549-3793549 - Au8 COSM5606450 c.3862C>T p.R1288W Substitution - Missense 16:3745329-3745329 - 2521243 COSM5886913 c.4174C>T p.R1392* Substitution - Nonsense 16:3739684-3739684 - S02285 COSM5663063 c.5892T>G p.R1964R Substitution - coding silent 16:3729155-3729155 - UM-SCC-47 COSM4600022 c.3274C>T p.Q1092* Substitution - Nonsense 16:3758949-3758949 - TCGA-CD-A4MJ-01 COSM4060691 c.6661A>G p.M2221V Substitution - Missense 16:3728386-3728386 - WSU COSM88742 c.4459C>T p.H1487Y Substitution - Missense 16:3736751-3736751 - C32 COSM352596 c.4648G>C p.E1550Q Substitution - Missense 16:3736116-3736116 - ESCC_36 COSM5628770 c.3986T>C p.L1329P Substitution - Missense 16:3740546-3740546 - DND-41 COSM96466 c.3710G>A p.C1237Y Substitution - Missense 16:3751795-3751795 - 2062 COSM88737 c.4305T>A p.D1435E Substitution - Missense 16:3738648-3738648 - 22_tFL COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - TCGA-BR-8487-01 COSM4060704 c.4804C>T p.R1602C Substitution - Missense 16:3731862-3731862 - TCGA-G3-A7M7-01 COSM4929926 c.1784A>G p.H595R Substitution - Missense 16:3780771-3780771 - HCC70 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 8016470 COSM3387435 c.5343C>T p.H1781H Substitution - coding silent 16:3729704-3729704 - TCGA-HU-A4GN-01 COSM4060701 c.4981A>G p.M1661V Substitution - Missense 16:3731383-3731383 - ESCC-078T COSM3937063 c.5386C>T p.Q1796* Substitution - Nonsense 16:3729661-3729661 - 2_FL COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - TCGA-32-2491-01 COSM3747999 c.2826T>C p.P942P Substitution - coding silent 16:3770624-3770624 - 587222 COSM1202272 c.1238G>A p.R413Q Substitution - Missense 16:3792073-3792073 - 428 COSM4433182 c.5278C>T p.Q1760* Substitution - Nonsense 16:3729769-3729769 - TCGA-BT-A20T-01 COSM417008 c.2659C>T p.Q887* Substitution - Nonsense 16:3770791-3770791 - CDGLIV0707A0251_T COSM5040607 c.4499A>T p.Q1500L Substitution - Missense 16:3736711-3736711 - YUKAT COSM5384870 c.2961G>A p.Q987Q Substitution - coding silent 16:3769273-3769273 - OSCC-GB_00610111 COSM4886682 c.6066G>A p.Q2022Q Substitution - coding silent 16:3728981-3728981 - TCGA-AG-A002-01 COSM260288 c.321G>A p.P107P Substitution - coding silent 16:3850774-3850774 - TCGA-A8-A097-01 COSM435237 c.5406G>C p.V1802V Substitution - coding silent 16:3729641-3729641 - HCC53 COSM1609323 c.1460C>A p.A487D Substitution - Missense 16:3782797-3782797 - 08-067 COSM305487 c.2191A>G p.N731D Substitution - Missense 16:3774661-3774661 - 9906_122 COSM303846 c.5712G>C p.Q1904H Substitution - Missense 16:3729335-3729335 - TCGA-AA-3715-01 COSM268947 c.5087A>G p.H1696R Substitution - Missense 16:3731277-3731277 - TCGA-D1-A15X-01 COSM970550 c.5698C>G p.P1900A Substitution - Missense 16:3729349-3729349 - TCGA-D1-A167-01 COSM970600 c.2015G>A p.R672H Substitution - Missense 16:3778109-3778109 - PA122 COSM1162478 c.1491G>A p.Q497Q Substitution - coding silent 16:3782766-3782766 - FL25 COSM88751 c.4448T>G p.I1483S Substitution - Missense 16:3736762-3736762 - ccRCC-84 COSM1661273 c.2567C>T p.T856I Substitution - Missense 16:3770883-3770883 - PD9364a COSM1563119 c.4134-1G>A p.? Unknown 16:3739725-3739725 - SCC-9 COSM4597500 c.6146C>A p.A2049D Substitution - Missense 16:3728901-3728901 - 2179 COSM88759 c.2254C>T p.Q752* Substitution - Nonsense 16:3774598-3774598 - CN-AML-08-T COSM148010 c.2784G>A p.P928P Substitution - coding silent 16:3770666-3770666 - 39_FL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - QC2-12-T2 COSM5045069 c.4507T>A p.Y1503N Substitution - Missense 16:3736703-3736703 - TCGA-AA-3510-01 COSM1377845 c.3505C>T p.R1169C Substitution - Missense 16:3757913-3757913 - GBM7 COSM4167427 c.5560C>T p.Q1854* Substitution - Nonsense 16:3729487-3729487 - TCGA-Q1-A73O-01 COSM4835292 c.4869C>A p.A1623A Substitution - coding silent 16:3731797-3731797 - B66 COSM254631 c.6983C>T p.S2328L Substitution - Missense 16:3728064-3728064 - ESO-632 COSM1249112 c.2528T>A p.L843Q Substitution - Missense 16:3770922-3770922 - Pat_41_B COSM5850890 c.4957G>A p.D1653N Substitution - Missense 16:3731407-3731407 - PD18047a COSM5787046 c.4277C>T p.T1426M Substitution - Missense 16:3739581-3739581 - QC2-35-T2 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - TCGA-AP-A054-01 COSM970566 c.4419delC p.C1474fs*76 Deletion - Frameshift 16:3736791-3736791 - T3021 COSM1180829 c.3250delA p.I1084fs*15 Deletion - Frameshift 16:3767720-3767720 - 2109 COSM88745 c.4508A>T p.Y1503F Substitution - Missense 16:3736702-3736702 - D28 COSM5544756 c.3552C>T p.V1184V Substitution - coding silent 16:3757866-3757866 - 1524370 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - CSCC-27-T COSM4518557 c.6967_6968GG>AA p.G2323K Substitution - Missense 16:3728079-3728080 - ccRCC-75 COSM1661274 c.1645T>G p.S549A Substitution - Missense 16:3781235-3781235 - 2000756 COSM1644511 c.4415G>C p.W1472S Substitution - Missense 16:3736795-3736795 - T3094 COSM4674640 c.6972G>T p.Q2324H Substitution - Missense 16:3728075-3728075 - Pat_76_B COSM5850895 c.2296_2297CC>TT p.P766F Substitution - Missense 16:3773917-3773918 - 10-76 COSM1645456 c.2861C>A p.A954D Substitution - Missense 16:3770589-3770589 - STC291 COSM5054882 c.5261G>A p.S1754N Substitution - Missense 16:3729786-3729786 - SH-4435 COSM96413 c.2678C>T p.S893L Substitution - Missense 16:3770772-3770772 - TCGA-B5-A11N-01 COSM970546 c.6310C>T p.R2104C Substitution - Missense 16:3728737-3728737 - 2492713 COSM5606450 c.3862C>T p.R1288W Substitution - Missense 16:3745329-3745329 - B37 COSM254627 c.310C>T p.Q104* Substitution - Nonsense 16:3850785-3850785 - 17802 COSM5346608 c.4275C>G p.N1425K Substitution - Missense 16:3739583-3739583 - 33t COSM88743 c.4507T>G p.Y1503D Substitution - Missense 16:3736703-3736703 - SC_9047 COSM5563434 c.6626A>C p.Q2209P Substitution - Missense 16:3728421-3728421 - TCGA-CD-A4MG-01 COSM4060715 c.2279C>A p.P760Q Substitution - Missense 16:3774573-3774573 - TCGA-BT-A20T-01 COSM396944 c.2499C>G p.L833L Substitution - coding silent 16:3770951-3770951 - T3021 COSM4674647 c.4163C>T p.S1388F Substitution - Missense 16:3739695-3739695 - S03-45671-TP COSM4990881 c.4963C>T p.L1655L Substitution - coding silent 16:3731401-3731401 - CHC1747T COSM4788085 c.4414T>A p.W1472R Substitution - Missense 16:3736796-3736796 - T1154 COSM4674658 c.335T>C p.M112T Substitution - Missense 16:3850760-3850760 - 2492722 COSM5724226 c.2867C>T p.P956L Substitution - Missense 16:3770583-3770583 - TCGA-46-3767-01 COSM703023 c.1464C>A p.L488L Substitution - coding silent 16:3782793-3782793 - 9906_129 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 9415 COSM5751472 c.1527_1528insA p.A510fs*18 Insertion - Frameshift 16:3782729-3782730 - ov519A COSM96418 c.4477delA p.I1493fs*57 Deletion - Frameshift 16:3736733-3736733 - 1524412 COSM96443 c.4499A>C p.Q1500P Substitution - Missense 16:3736711-3736711 - YUKLAB COSM1708695 c.3367C>T p.P1123S Substitution - Missense 16:3758856-3758856 - TCGA-28-2514-01 COSM3402317 c.5986G>A p.A1996T Substitution - Missense 16:3729061-3729061 - HT115 COSM260288 c.321G>A p.P107P Substitution - coding silent 16:3850774-3850774 - 39_tFL COSM4170759 c.3982+2T>A p.? Unknown 16:3744892-3744892 - TCGA-EK-A3GK-01 COSM4852899 c.3187G>T p.E1063* Substitution - Nonsense 16:3767783-3767783 - TCGA-DR-A0ZM-01 COSM460547 c.637C>T p.L213F Substitution - Missense 16:3850458-3850458 - Pfieffer COSM166408 c.4471C>A p.Q1491K Substitution - Missense 16:3736739-3736739 - I2L-P19Tb-Tumor-Organoid COSM2919923 c.5552G>A p.R1851H Substitution - Missense 16:3729495-3729495 - PAPLDL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-66-2793-01 COSM703033 c.4303G>T p.D1435Y Substitution - Missense 16:3738650-3738650 - SHIN-3 COSM96507 c.3837-26_3837-5del22 p.? Unknown 16:3745359-3745380 - V-PH-08T COSM4770345 c.7329G>T p.*2443Y Nonstop extension 16:3727718-3727718 - ICGC_MB68 COSM88738 c.4337G>T p.R1446L Substitution - Missense 16:3738616-3738616 - ESO-251 COSM1249111 c.6727G>A p.A2243T Substitution - Missense 16:3728320-3728320 - KM12 COSM417011 c.4990C>T p.R1664C Substitution - Missense 16:3731374-3731374 - TCGA-B6-A1KF-01 COSM1478867 c.4778C>A p.T1593N Substitution - Missense 16:3731888-3731888 - TCGA-AP-A051-01 COSM970604 c.1874G>A p.R625H Substitution - Missense 16:3778767-3778767 - Au4 COSM5603283 c.6080C>T p.P2027L Substitution - Missense 16:3728967-3728967 - PD6080a COSM2919921 c.5573G>A p.R1858H Substitution - Missense 16:3729474-3729474 - MD-325 COSM88738 c.4337G>T p.R1446L Substitution - Missense 16:3738616-3738616 - PD11148a COSM5945320 c.1501C>T p.Q501* Substitution - Nonsense 16:3782756-3782756 - TCGA-AP-A051-01 COSM970548 c.6281C>T p.P2094L Substitution - Missense 16:3728766-3728766 - Pa14C COSM84329 c.6841G>A p.A2281T Substitution - Missense 16:3728206-3728206 - TCGA-CM-6171-01 COSM1377832 c.4213G>A p.V1405M Substitution - Missense 16:3739645-3739645 - TCGA-A2-A1G1-01 COSM1478869 c.2114A>G p.N705S Substitution - Missense 16:3777657-3777657 - 39_tFL COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-HU-A4H0-01 COSM4060706 c.4624G>A p.G1542S Substitution - Missense 16:3736140-3736140 - CP66-MEL COSM21712 c.2809C>T p.P937S Substitution - Missense 16:3770641-3770641 - QC2-12-T2 COSM5656311 c.4788delC p.N1596fs*39 Deletion - Frameshift 16:3731878-3731878 - CHC2351T COSM4801224 c.681T>A p.P227P Substitution - coding silent 16:3850414-3850414 - TCGA-D5-6540-01 COSM1377846 c.3493T>C p.W1165R Substitution - Missense 16:3757925-3757925 - TCGA-EK-A3GK-01 COSM4852995 c.3172G>T p.E1058* Substitution - Nonsense 16:3767798-3767798 - 37_tFL COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - FL012 COSM220496 c.4307G>A p.S1436N Substitution - Missense 16:3738646-3738646 - 587382 COSM1202276 c.7037C>T p.P2346L Substitution - Missense 16:3728010-3728010 - 304_T COSM3957567 c.1823+4C>A p.? Unknown 16:3780728-3780728 - CSCC-49-T COSM4569929 c.2172T>C p.F724F Substitution - coding silent 16:3774680-3774680 - S06-38853-TP COSM4990886 c.3395C>T p.P1132L Substitution - Missense 16:3758023-3758023 - 2492711 COSM5606450 c.3862C>T p.R1288W Substitution - Missense 16:3745329-3745329 - 7313 COSM5614349 c.3776A>G p.Q1259R Substitution - Missense 16:3751729-3751729 - 8014753 COSM218493 c.2950A>C p.N984H Substitution - Missense 16:3769284-3769284 - 1524426 COSM96447 c.? p.G2229S Substitution - Missense 026-08-01TD COSM5416700 c.4599T>C p.S1533S Substitution - coding silent 16:3736165-3736165 - Gp5D COSM2919930 c.5410C>T p.H1804Y Substitution - Missense 16:3729637-3729637 - tumor_4144951 COSM5948954 c.4308T>A p.S1436R Substitution - Missense 16:3738645-3738645 - Patient_1_Relapse COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-BR-4184-01 COSM4060700 c.4992C>T p.R1664R Substitution - coding silent 16:3731372-3731372 - SNUH_G73_S1 COSM148010 c.2784G>A p.P928P Substitution - coding silent 16:3770666-3770666 - TCGA-CG-5721-01 COSM4060717 c.1854C>T p.P618P Substitution - coding silent 16:3778787-3778787 - PTC-515C COSM4129053 c.5670C>T p.P1890P Substitution - coding silent 16:3729377-3729377 - S07-16280-TP COSM4990889 c.1828C>T p.Q610* Substitution - Nonsense 16:3778813-3778813 - TCGA-BR-8680-01 COSM2919990 c.3506G>A p.R1169H Substitution - Missense 16:3757912-3757912 - NCI-ADR-RES COSM1678809 c.2678C>A p.S893* Substitution - Nonsense 16:3770772-3770772 - TCGA-AX-A0J1-01 COSM970614 c.732G>A p.T244T Substitution - coding silent 16:3850363-3850363 - PT55 COSM5942648 c.4198G>A p.E1400K Substitution - Missense 16:3739660-3739660 - I2L-P19Ta-Tumor-Biopsy COSM2920035 c.1802G>A p.R601Q Substitution - Missense 16:3780753-3780753 - 1518 COSM88752 c.4496T>C p.L1499P Substitution - Missense 16:3736714-3736714 - YUPAT COSM1708694 c.3368C>T p.P1123L Substitution - Missense 16:3758855-3758855 - TCGA-04-1525-01 COSM111631 c.2978delC p.P993fs*5 Deletion - Frameshift 16:3769256-3769256 - TCGA-GV-A3JV-01 COSM1301955 c.5895G>A p.E1965E Substitution - coding silent 16:3729152-3729152 - T1154 COSM4674650 c.3135A>G p.P1045P Substitution - coding silent 16:3767835-3767835 - tumor_4136702 COSM5947980 c.1775G>A p.W592* Substitution - Nonsense 16:3780780-3780780 - TCGA-34-2600-01 COSM126635 c.1507C>T p.Q503* Substitution - Nonsense 16:3782750-3782750 - 1524425 COSM96447 c.? p.G2229S Substitution - Missense 4_FL COSM4170754 c.4451T>C p.F1484S Substitution - Missense 16:3736759-3736759 - OCI-Ly8 COSM88769 c.3301_3302delCT p.L1101fs*26 Deletion - Frameshift 16:3758921-3758922 - H1703 COSM1196579 c.4416G>T p.W1472C Substitution - Missense 16:3736794-3736794 - T3225 COSM4674651 c.2879C>T p.P960L Substitution - Missense 16:3770571-3770571 - LPJ108 COSM88748 c.4337G>A p.R1446H Substitution - Missense 16:3738616-3738616 - TCGA-D3-A3MU-06 COSM3509547 c.7281C>T p.V2427V Substitution - coding silent 16:3727766-3727766 - PD8203a COSM5945321 c.1216+5G>A p.? Unknown 16:3793381-3793381 - S17_pre COSM5574530 c.5888A>G p.E1963G Substitution - Missense 16:3729159-3729159 - 6115115 COSM5563114 c.2962C>A p.P988T Substitution - Missense 16:3769272-3769272 - 2492720 COSM5724226 c.2867C>T p.P956L Substitution - Missense 16:3770583-3770583 - UM-SCC-17B COSM96455 c.5282C>G p.S1761* Substitution - Nonsense 16:3729765-3729765 - T3498 COSM2920000 c.3250_3250+1insA p.I1084fs*3 Unknown 16:3767719-3767720 - TCGA-18-3407-01 COSM703032 c.4223G>A p.C1408Y Substitution - Missense 16:3739635-3739635 - TCGA-EE-A29D-06 COSM3888514 c.4652A>G p.E1551G Substitution - Missense 16:3736112-3736112 - 228 COSM166406 c.4231G>A p.G1411R Substitution - Missense 16:3739627-3739627 - 1524432 COSM96449 c.? p.I2101M Substitution - Missense TCGA-DU-6405-01 COSM3957564 c.5048G>C p.R1683P Substitution - Missense 16:3731316-3731316 - LUAD-S01302 COSM395599 c.2510G>T p.G837V Substitution - Missense 16:3770940-3770940 - B105-Tumor COSM88760 c.3517C>T p.R1173* Substitution - Nonsense 16:3757901-3757901 - LB2518-MEL COSM21764 c.5271C>T p.G1757G Substitution - coding silent 16:3729776-3729776 - TCGA-AZ-6599-01 COSM1377864 c.356G>T p.G119V Substitution - Missense 16:3850739-3850739 - VAL COSM88758 c.694C>T p.Q232* Substitution - Nonsense 16:3850401-3850401 - TCGA-D8-A1XQ-01 COSM3817961 c.5063C>T p.T1688M Substitution - Missense 16:3731301-3731301 - LP6007533-DNA_A01 COSM5032981 c.3729G>A p.E1243E Substitution - coding silent 16:3751776-3751776 - TCGA-BP-4762-01 COSM3361761 c.2809C>A p.P937T Substitution - Missense 16:3770641-3770641 - CHC892T COSM4961351 c.6292G>A p.A2098T Substitution - Missense 16:3728755-3728755 - PT14_1 COSM2919990 c.3506G>A p.R1169H Substitution - Missense 16:3757912-3757912 - TCGA-16-0861-01 COSM3747999 c.2826T>C p.P942P Substitution - coding silent 16:3770624-3770624 - TCGA-A6-6781-01 COSM1377812 c.6072G>A p.A2024A Substitution - coding silent 16:3728975-3728975 - T3182 COSM4674656 c.711C>T p.S237S Substitution - coding silent 16:3850384-3850384 - SJHYPO146_D COSM3420981 c.3832G>A p.E1278K Substitution - Missense 16:3749631-3749631 - FL7 COSM88764 c.3375T>A p.Y1125* Substitution - Nonsense 16:3758043-3758043 - TCGA-04-1338-01 COSM77521 c.4135T>G p.F1379V Substitution - Missense 16:3739723-3739723 - DLBCL827 COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - 38_tFL COSM88749 c.4336C>T p.R1446C Substitution - Missense 16:3738617-3738617 - TCGA-BR-4362-01 COSM1377819 c.4874T>C p.M1625T Substitution - Missense 16:3731792-3731792 - QC2-32-T2 COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - LAU618 COSM234574 c.714G>C p.V238V Substitution - coding silent 16:3850381-3850381 - CSCC-18-T COSM1161163 c.4243C>T p.Q1415* Substitution - Nonsense 16:3739615-3739615 - 10-76 COSM1645457 c.2731C>T p.Q911* Substitution - Nonsense 16:3770719-3770719 - XHDG48C COSM4767473 c.6479C>T p.A2160V Substitution - Missense 16:3728568-3728568 - tumor_4189200 COSM88744 c.4507T>C p.Y1503H Substitution - Missense 16:3736703-3736703 - DM42 COSM5608146 c.2389A>T p.N797Y Substitution - Missense 16:3773825-3773825 - TCGA-BR-A4J7-01 COSM4060692 c.6621A>G p.Q2207Q Substitution - coding silent 16:3728426-3728426 - 1093 COSM1159754 c.4492C>T p.R1498* Substitution - Nonsense 16:3736718-3736718 - TCGA-EE-A2MR-06 COSM3509553 c.5333C>T p.S1778L Substitution - Missense 16:3729714-3729714 - TCGA-BG-A0VZ-01 COSM970590 c.2811G>A p.P937P Substitution - coding silent 16:3770639-3770639 - DM18 COSM5608141 c.4240G>A p.V1414I Substitution - Missense 16:3739618-3739618 - tumor_4112447 COSM4260243 c.4471C>G p.Q1491E Substitution - Missense 16:3736739-3736739 - SNUH_G45_S1 COSM3679906 c.2705C>T p.T902I Substitution - Missense 16:3770745-3770745 - 133T COSM5576011 c.5447G>T p.C1816F Substitution - Missense 16:3729600-3729600 - 1524428 COSM96448 c.? p.P858S Substitution - Missense TCGA-AA-3715-01 COSM293624 c.5219A>G p.H1740R Substitution - Missense 16:3729828-3729828 - TCGA-D7-A4Z0-01 COSM4060698 c.5404G>A p.V1802M Substitution - Missense 16:3729643-3729643 - C0061T COSM4151332 c.3988C>G p.Q1330E Substitution - Missense 16:3740544-3740544 - TCGA-BR-8081-01 COSM4060714 c.2438C>T p.P813L Substitution - Missense 16:3773776-3773776 - TCGA-EB-A3XD-01 COSM3509549 c.7067C>T p.S2356F Substitution - Missense 16:3727980-3727980 - 2106 COSM88760 c.3517C>T p.R1173* Substitution - Nonsense 16:3757901-3757901 - ESCC-008T COSM1377819 c.4874T>C p.M1625T Substitution - Missense 16:3731792-3731792 - B5 COSM254628 c.1063C>T p.Q355* Substitution - Nonsense 16:3793539-3793539 - T613 COSM2920000 c.3250_3250+1insA p.I1084fs*3 Unknown 16:3767719-3767720 - 1546 COSM88774 c.3059A>T p.E1020V Substitution - Missense 16:3769175-3769175 - MKB-1 COSM96457 c.6418C>T p.Q2140* Substitution - Nonsense 16:3728629-3728629 - B13 COSM254626 c.3874C>T p.Q1292* Substitution - Nonsense 16:3745317-3745317 - 53 COSM5762853 c.4459C>A p.H1487N Substitution - Missense 16:3736751-3736751 - HCC011T COSM5819992 c.1915G>T p.D639Y Substitution - Missense 16:3778726-3778726 - SJHYPO032 COSM1377845 c.3505C>T p.R1169C Substitution - Missense 16:3757913-3757913 - SJMB028 COSM255965 c.1447C>T p.R483* Substitution - Nonsense 16:3782810-3782810 - S00539 COSM317183 c.3697A>T p.R1233W Substitution - Missense 16:3757289-3757289 - REX COSM96464 c.4071delT p.F1358fs*18 Deletion - Frameshift 16:3740461-3740461 - DM74 COSM254631 c.6983C>T p.S2328L Substitution - Missense 16:3728064-3728064 - 520 COSM5612099 c.913A>C p.N305H Substitution - Missense 16:3810665-3810665 - TCGA-AX-A0J1-01 COSM970542 c.6441T>G p.A2147A Substitution - coding silent 16:3728606-3728606 - DM14 COSM5608138 c.175C>T p.L59F Substitution - Missense 16:3850920-3850920 - WSU-HN8 COSM4603421 c.586_587insT p.S196fs*4 Insertion - Frameshift 16:3850508-3850509 - ICGC_PA110 COSM3670194 c.5383T>C p.C1795R Substitution - Missense 16:3729664-3729664 - 7_tFL COSM291735 c.5039_5041delCCT p.S1680delS Deletion - In frame 16:3731323-3731325 - CSB1 COSM5028062 c.5433G>A p.K1811K Substitution - coding silent 16:3729614-3729614 - ESCC_BICR_054T COSM5444217 c.3217C>G p.Q1073E Substitution - Missense 16:3767753-3767753 - ESCC-011T COSM3937064 c.1873C>T p.R625C Substitution - Missense 16:3778768-3778768 - 7T COSM2919954 c.4690A>G p.K1564E Substitution - Missense 16:3736074-3736074 - TCGA-BR-8372-01 COSM4060699 c.5166G>A p.V1722V Substitution - coding silent 16:3731198-3731198 - TCGA-BG-A0VT-01 COSM970562 c.4545C>G p.I1515M Substitution - Missense 16:3736665-3736665 - DM58 COSM5608147 c.1076T>C p.V359A Substitution - Missense 16:3793526-3793526 - WSU-NHL COSM88742 c.4459C>T p.H1487Y Substitution - Missense 16:3736751-3736751 - TCGA-A3-3316-01 COSM1493694 c.2686G>A p.G896R Substitution - Missense 16:3770764-3770764 - TCGA-EI-6917-01 COSM3420982 c.1990G>T p.E664* Substitution - Nonsense 16:3778134-3778134 - B105 COSM88760 c.3517C>T p.R1173* Substitution - Nonsense 16:3757901-3757901 - LC_S25 COSM1189166 c.4008C>G p.N1336K Substitution - Missense 16:3740524-3740524 - T3094 COSM4674639 c.7059G>T p.R2353R Substitution - coding silent 16:3727988-3727988 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.459725;Hs.459726;Hs.459759 16p13.3 600140

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.85+8601T>G 16 3921232 CLL A C Missense p.F1379V c.4135T>G 16 3789724 OV A C Missense p.I1437M c.4311T>G 16 3788643 UCEC A C Missense p.I314S c.941T>G 16 3860638 CM A C Missense p.L2330R c.6989T>G 16 3778059 LUSC A C Missense p.Y1450D c.4348T>G 16 3788606 LUSC A C Missense p.Y1503D c.4507T>G 16 3786704 DLBCL A C Nonsense p.Y1539* c.4617T>G 16 3786148 BLCA A - Frameshift p.F1410Lfs*49 c.4230delT 16 3789629 STAD AGG - InFrameDeletion p.S1680delS c.5039_5041delCCT 16 3781324 HNSC A G Missense p.C1795R c.5383T>C 16 3779665 PIA A G Missense p.F1484S c.4451T>C 16 3786760 BLCA A G Missense p.I1453T c.4358T>C 16 3788596 OV A G Missense p.L1338S c.4013T>C 16 3790520 OV A G Missense p.V1192A c.3575T>C 16 3807844 GBM A G Missense p.V1295A c.3884T>C 16 3795308 CM A G Missense p.V293A c.878T>C 16 3860701 RCCC A G Missense p.Y1503H c.4507T>C 16 3786704 DLBCL A G SpliceDonorSNV . c.4280+2T>C 16 3789577 SCLC A G Synonymous p.G777G c.2331T>C 16 3823884 LUSC A G Synonymous p.H1485H c.4455T>C 16 3786756 PRAD A G Synonymous p.I1431I c.4293T>C 16 3788661 DLBCL A G Synonymous p.P942P c.2826T>C 16 3820625 GBM A G Synonymous p.S1533S c.4599T>C 16 3786166 CLL ATGTGATTCAAAACGTTT - InFrameDeletion p.N390_M395delNVLNHM c.1167_1184delAAACGTTTTGAATCACAT 16 3843419 ALL A T Missense p.L1434Q c.4301T>A 16 3788653 DLBCL A T Missense p.L843Q c.2528T>A 16 3820923 ESCA A T Nonsense p.L654* c.1961T>A 16 3828164 MB A T Nonsense p.L673* c.2018T>A 16 3828107 THCA C A Missense p.D1435Y c.4303G>T 16 3788651 LUSC C A Missense p.D1521Y c.4561G>T 16 3786204 HNSC C A Missense p.G1383V c.4148G>T 16 3789711 PRAD C A Missense p.G1404V c.4211G>T 16 3789648 UCEC C A Missense p.G2019W c.6055G>T 16 3778993 CM C A Missense p.G401W c.1201G>T 16 3843402 CM C A Missense p.G57V c.170G>T 16 3900926 LUSC C A Missense p.V1634L c.4900G>T 16 3781465 HNSC C A Nonsense p.E1561* c.4681G>T 16 3786084 NB C A Nonsense p.G2398* c.7192G>T 16 3777856 UCEC C A SpliceAcceptorSNV . c.3983-1G>T 16 3790551 BRCA C A Synonymous p.P901P c.2703G>T 16 3820748 LUAD CC TT Missense p.A698T c.2091_2092delinsAA 16 3828033 CM C - Frameshift p.R386Qfs*3 c.1157delG 16 3843446 GBM C G Missense p.A234P c.700G>C 16 3900396 HNSC C G Missense p.A254P c.760G>C 16 3900336 HNSC C G Missense p.D1143H c.3427G>C 16 3807992 BLCA C G Missense p.E1243D c.3729G>C 16 3801777 HNSC C G Missense p.E666Q c.1996G>C 16 3828129 BLCA C G Missense p.G174R c.520G>C 16 3900576 LUAD C G Missense p.Q1994H c.5982G>C 16 3779066 BRCA C G Missense p.R1683P c.5048G>C 16 3781317 LGG C G Missense p.R2104P c.6311G>C 16 3778737 CM C G Missense p.R702T c.2105G>C 16 3828020 HNSC C G Missense p.V406L c.1216G>C 16 3843387 PAAD C G Missense p.V694L c.2080G>C 16 3828045 BLCA C G Synonymous p.V1467V c.4401G>C 16 3786810 OV C G Synonymous p.V1802V c.5406G>C 16 3779642 BRCA C T Missense p.A1782T c.5344G>A 16 3779704 UCEC C T Missense p.A179T c.535G>A 16 3900561 STAD C T Missense p.A1824T c.5470G>A 16 3779578 SCLC C T Missense p.A1996T c.5986G>A 16 3779062 GBM C T Missense p.A2243T c.6727G>A 16 3778321 ESCA C T Missense p.A259T c.775G>A 16 3900321 UCEC C T Missense p.A884T c.2650G>A 16 3820801 OV C T Missense p.A966T c.2896G>A 16 3819339 STAD C T Missense p.C1200Y c.3599G>A 16 3807820 MB C T Missense p.C1408Y c.4223G>A 16 3789636 LUSC C T Missense p.D1481N c.4441G>A 16 3786770 HNSC C T Missense p.E1023K c.3067G>A 16 3817904 HNSC C T Missense p.E1478K c.4432G>A 16 3786779 CM C T Missense p.G1069D c.3206G>A 16 3817765 LUAD C T Missense p.G79S c.235G>A 16 3900861 BLCA C T Missense p.R1081H c.3242G>A 16 3817729 BRCA C T Missense p.R1140Q c.3419G>A 16 3808000 LUSC C T Missense p.R1446H c.4337G>A 16 3788617 HNSC C T Missense p.R1800Q c.5399G>A 16 3779649 CM C T Missense p.R2151Q c.6452G>A 16 3778596 ESCA C T Missense p.S1436N c.4307G>A 16 3788647 BLCA C T Nonsense p.W1502* c.4505G>A 16 3786706 BLCA C T Nonsense p.W419* c.1256G>A 16 3842056 GBM C T SpliceAcceptorSNV . c.4395-1G>A 16 3786817 SCLC C T Synonymous p.A2265A c.6795G>A 16 3778253 PRAD C T Synonymous p.E1562E c.4686G>A 16 3786079 BRCA C T Synonymous p.E1965E c.5895G>A 16 3779153 BLCA C T Synonymous p.K1811K c.5433G>A 16 3779615 BRCA C T Synonymous p.K266K c.798G>A 16 3900298 CM C T Synonymous p.L2000L c.6000G>A 16 3779048 HNSC C T Synonymous p.P1817P c.5451G>A 16 3779597 STAD C T Synonymous p.P2150P c.6450G>A 16 3778598 NSCLC C T Synonymous p.P2363P c.7089G>A 16 3777959 UCEC C T Synonymous p.P688P c.2064G>A 16 3828061 CM C T Synonymous p.P937P c.2811G>A 16 3820640 UCEC C T Synonymous p.T2434T c.7302G>A 16 3777746 BLCA C T Synonymous p.V701V c.2103G>A 16 3828022 LUSC CTTT - IntronicDeletion . c.4560+114_4560+117delAAAG 16 3786534 ESCA GAAATAGCTATATACTTACGGTT - SpliceDonorDeletion . c.3833_3836+19delAACCGTAAGTATATAGCTATTTC 16 3799609 ALL GAGGCCC - Frameshift p.G837Rfs*10 c.2509_2515delGGGCCTC 16 3820936 OV G A Missense p.A2160V c.6479C>T 16 3778569 LUAD G A Missense p.A2281T c.6841G>A 16 3778207 PAAD G A Missense p.P1903S c.5707C>T 16 3779341 CM G A Missense p.P2094L c.6281C>T 16 3778767 UCEC G A Missense p.P2363L c.7088C>T 16 3777960 CM G A Missense p.P2410L c.7229C>T 16 3777819 CM G A Missense p.P344L c.1031C>T 16 3843572 CM G A Missense p.P583S c.1747C>T 16 3830809 HNSC G A Missense p.P746S c.2236C>T 16 3824617 CM G A Missense p.P814L c.2441C>T 16 3823774 LUSC G A Missense p.P855L c.2564C>T 16 3820887 CM G A Missense p.P928S c.2782C>T 16 3820669 CM G A Missense p.P988L c.2963C>T 16 3819272 CM G A Missense p.R1091C c.3271C>T 16 3808953 BRCA G A Missense p.R1112W c.3334C>T 16 3808890 BRCA G A Missense p.R1169C c.3505C>T 16 3807914 ALL G A Missense p.R1347W c.4039C>T 16 3790494 GBM G A Missense p.R1446C c.4336C>T 16 3788618 ALL G A Missense p.R1446C c.4336C>T 16 3788618 CM G A Missense p.R1446C c.4336C>T 16 3788618 LUSC G A Missense p.R1446C c.4336C>T 16 3788618 MB G A Missense p.R1664C c.4990C>T 16 3781375 BLCA G A Missense p.R2104C c.6310C>T 16 3778738 PRAD G A Missense p.S1614F c.4841C>T 16 3781826 HNSC G A Missense p.S1767L c.5300C>T 16 3779748 LUSC G A Missense p.S2328L c.6983C>T 16 3778065 CLL G A Missense p.S2372L c.7115C>T 16 3777933 BRCA G A Missense p.S326F c.977C>T 16 3843626 RCCC G A Missense p.T872M c.2615C>T 16 3820836 STAD G A Missense p.T950M c.2849C>T 16 3820602 HNSC G A Nonsense p.Q104* c.310C>T 16 3900786 CLL G A Nonsense p.Q1152* c.3454C>T 16 3807965 BLCA G A Nonsense p.Q1292* c.3874C>T 16 3795318 CLL G A Nonsense p.Q1415* c.4243C>T 16 3789616 DLBCL G A Nonsense p.Q1756* c.5266C>T 16 3779782 LUAD G A Nonsense p.Q2085* c.6253C>T 16 3778795 STAD G A Nonsense p.Q355* c.1063C>T 16 3843540 CLL G A Nonsense p.Q503* c.1507C>T 16 3832751 HNSC G A Nonsense p.Q503* c.1507C>T 16 3832751 LUSC G A Nonsense p.Q887* c.2659C>T 16 3820792 BLCA G A Nonsense p.Q911* c.2731C>T 16 3820720 CM G A Nonsense p.Q943* c.2827C>T 16 3820624 LUSC G A Nonsense p.R1319* c.3955C>T 16 3794922 MB G A Nonsense p.R1341* c.4021C>T 16 3790512 COREAD G A Nonsense p.R1341* c.4021C>T 16 3790512 OV G A Nonsense p.R1360* c.4078C>T 16 3790455 STAD G A Synonymous p.D1156D c.3468C>T 16 3807951 STAD G A Synonymous p.D1403D c.4209C>T 16 3789650 ESCA G A Synonymous p.F1280F c.3840C>T 16 3795352 CM G A Synonymous p.G2120G c.6360C>T 16 3778688 CM G A Synonymous p.I2335I c.7005C>T 16 3778043 CM G A Synonymous p.L604L c.1810C>T 16 3830746 LUSC G A Synonymous p.L708L c.2122C>T 16 3827650 CM G A Synonymous p.N2402N c.7206C>T 16 3777842 CM G A Synonymous p.P2064P c.6192C>T 16 3778856 HNSC G A Synonymous p.P726P c.2178C>T 16 3824675 COREAD G A Synonymous p.S2362S c.7086C>T 16 3777962 CM G A Synonymous p.S480S c.1440C>T 16 3832818 CM G A Synonymous p.T2073T c.6219C>T 16 3778829 CM G A Synonymous p.V2427V c.7281C>T 16 3777767 CM G A Synonymous p.V2427V c.7281C>T 16 3777767 HNSC G C Missense p.I1515M c.4545C>G 16 3786666 UCEC G C Missense p.I2101M c.6303C>G 16 3778745 BRCA G C Missense p.L1556V c.4666C>G 16 3786099 HNSC G C Missense p.P1110R c.3329C>G 16 3808895 CM G C Missense p.P383R c.1148C>G 16 3843455 LUSC G C Missense p.P616R c.1847C>G 16 3828795 LUSC G C Missense p.P960R c.2879C>G 16 3820572 HNSC G C Missense p.Q2023E c.6067C>G 16 3778981 PRAD G C Missense p.Q2318E c.6952C>G 16 3778096 CLL G C Nonsense p.S1074* c.3221C>G 16 3817750 BLCA G C Nonsense p.S889* c.2666C>G 16 3820785 BLCA G C Synonymous p.L2090L c.6270C>G 16 3778778 LUAD G C Synonymous p.L833L c.2499C>G 16 3820952 BLCA G C Synonymous p.L869L c.2607C>G 16 3820844 HNSC G C Synonymous p.P94P c.282C>G 16 3900814 CM G C Synonymous p.V1704V c.5112C>G 16 3781253 HNSC GCT - InFrameDeletion p.Q2248delQ c.6743_6745delAGC 16 3778303 CM G - Frameshift p.C1474Vfs*76 c.4419delC 16 3786792 UCEC G - Frameshift p.P993Lfs*5 c.2978delC 16 3819257 OV GG AA Missense p.S802F c.2405_2406delinsTT 16 3823809 CM G T Missense p.F1439L c.4317C>A 16 3788637 UCEC G T Missense p.H2384Q c.7152C>A 16 3777896 LUSC G T Missense p.L2291M c.6871C>A 16 3778177 UCEC G T Missense p.P1208T c.3622C>A 16 3807365 RCCC G T Missense p.P12H c.35C>A 16 3929883 CLL G T Missense p.P937T c.2809C>A 16 3820642 RCCC G T Missense p.P993H c.2978C>A 16 3819257 CM G T Missense p.Q1491K c.4471C>A 16 3786740 MB G T Missense p.R1169S c.3505C>A 16 3807914 STAD G T Missense p.T1593N c.4778C>A 16 3781889 BRCA G T Nonsense p.C1808* c.5424C>A 16 3779624 COREAD G T Nonsense p.C1819* c.5457C>A 16 3779591 HNSC G T Nonsense p.S1365* c.4094C>A 16 3790439 NB G T Synonymous p.L488L c.1464C>A 16 3832794 LUSC G T Synonymous p.V1631V c.4893C>A 16 3781472 COREAD TA AC MultiAAMissense p.S1436_I1437delinsRF c.4308_4309delinsGT 16 3788645 HNSC T A Missense p.I1483F c.4447A>T 16 3786764 MB T A Missense p.N190I c.569A>T 16 3900527 CM T A Missense p.Q2230L c.6689A>T 16 3778359 HNSC T A Missense p.R1233W c.3697A>T 16 3807290 SCLC T A Missense p.S2315C c.6943A>T 16 3778105 LUSC T A Nonsense p.K1495* c.4483A>T 16 3786728 UCEC T A Nonsense p.K420* c.1258A>T 16 3842054 CLL T A Synonymous p.G284G c.852A>T 16 3860727 CM T A Synonymous p.I86I c.258A>T 16 3900838 CM T C 3-UTRSNV . c.7326+1001A>G 16 3776721 HC T C Missense p.N705S c.2114A>G 16 3827658 BRCA T C Missense p.Q1259R c.3776A>G 16 3801730 NSCLC T C Missense p.T228A c.682A>G 16 3900414 LUSC T C Missense p.Y1102C c.3305A>G 16 3808919 STAD T C Missense p.Y1230C c.3689A>G 16 3807298 CLL T C Missense p.Y1298C c.3893A>G 16 3795299 LUSC T C Missense p.Y1450C c.4349A>G 16 3788605 HNSC - T Frameshift p.N797Kfs*35 c.2390dupA 16 3823825 BRCA - T Frameshift p.R369Efs*58 c.1103dupA 16 3843500 UCEC T G Missense p.N984H c.2950A>C 16 3819285 PAAD T G Missense p.T1624P c.4870A>C 16 3781797 COREAD T G Missense p.Y1503S c.4508A>C 16 3786703 DLBCL T G Synonymous p.T1144T c.3432A>C 16 3807987 STAD - T IntronicInsertion . c.2464-91dupA 16 3821078 CM TTGCTGCTGCTGC - Frameshift p.Q2199Hfs*99 c.6597_6609delGCAGCAGCAGCAA 16 3778439 PRAD