Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 17 1631404 1631404 + Missense_Mutation SNP C C G TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr17:1631404C>G c.3151C>G c.(3151-3153)Ccc>Gcc p.P1051A BLCA 17 1631642 1631642 + Frame_Shift_Del DEL C C - TCGA-GC-A3I6-01A-11D-A20D-08 TCGA-GC-A3I6-10A-01D-A20D-08 g.chr17:1631642delC c.3389delC c.(3388-3390)gccfs p.A1130fs BLCA 17 1631759 1631759 + Missense_Mutation SNP A A G TCGA-K4-A3WV-01A-11D-A22Z-08 TCGA-K4-A3WV-10A-01D-A22Z-08 g.chr17:1631759A>G c.3506A>G c.(3505-3507)gAg>gGg p.E1169G BLCA 17 1633731 1633731 + Missense_Mutation SNP C C G TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr17:1633731C>G c.3725C>G c.(3724-3726)tCt>tGt p.S1242C BLCA 17 1634499 1634499 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr17:1634499C>G c.4104C>G c.(4102-4104)atC>atG p.I1368M BLCA 17 1634506 1634506 + Missense_Mutation SNP G G A TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr17:1634506G>A c.4111G>A c.(4111-4113)Gag>Aag p.E1371K BLCA 17 1635658 1635658 + Silent SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr17:1635658G>A c.4197G>A c.(4195-4197)gtG>gtA p.V1399V BLCA 17 1635761 1635761 + Nonsense_Mutation SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr17:1635761C>T c.4300C>T c.(4300-4302)Cag>Tag p.Q1434* BLCA 17 1636047 1636047 + Missense_Mutation SNP G G A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr17:1636047G>A c.4411G>A c.(4411-4413)Gcc>Acc p.A1471T BLCA 17 1636082 1636082 + Silent SNP G G A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr17:1636082G>A c.4446G>A c.(4444-4446)ctG>ctA p.L1482L BLCA 17 1636853 1636853 + Missense_Mutation SNP G G A TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr17:1636853G>A c.4522G>A c.(4522-4524)Gag>Aag p.E1508K BLCA 17 1637095 1637095 + Silent SNP G G C TCGA-LC-A66R-01A-41D-A30E-08 TCGA-LC-A66R-10A-01D-A30H-08 g.chr17:1637095G>C c.4764G>C c.(4762-4764)gtG>gtC p.V1588V BLCA 17 1637151 1637151 + Missense_Mutation SNP C C T TCGA-CF-A47S-01A-11D-A23U-08 TCGA-CF-A47S-10A-01D-A23U-08 g.chr17:1637151C>T c.4820C>T c.(4819-4821)cCg>cTg p.P1607L BLCA 17 1637420 1637420 + Missense_Mutation SNP C C A TCGA-E7-A6ME-01A-22D-A32B-08 TCGA-E7-A6ME-10B-01D-A329-08 g.chr17:1637420C>A c.5089C>A c.(5089-5091)Cgc>Agc p.R1697S BLCA 17 1639411 1639411 + Missense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr17:1639411G>A c.5404G>A c.(5404-5406)Gtg>Atg p.V1802M BLCA 17 1640893 1640893 + Missense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr17:1640893G>A c.5740G>A c.(5740-5742)Ggc>Agc p.G1914S BRCA 17 1628873 1628874 + Frame_Shift_Ins INS - - C TCGA-AN-A0FF-01A-11W-A050-09 TCGA-AN-A0FF-10A-01W-A055-09 g.chr17:1628873_1628874insC c.620_621insC c.(619-624)tgccccfs p.CP207fs BRCA 17 1630415 1630415 + Missense_Mutation SNP T T G TCGA-AO-A129-01A-21D-A10M-09 TCGA-AO-A129-10A-01D-A10M-09 g.chr17:1630415T>G c.2162T>G c.(2161-2163)cTt>cGt p.L721R BRCA 17 1630714 1630714 + Missense_Mutation SNP G G A TCGA-BH-A0BL-01A-11D-A10Y-09 TCGA-BH-A0BL-11A-12D-A10Y-09 g.chr17:1630714G>A c.2461G>A c.(2461-2463)Gtg>Atg p.V821M BRCA 17 1636026 1636026 + Missense_Mutation SNP C C G TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr17:1636026C>G c.4390C>G c.(4390-4392)Cag>Gag p.Q1464E BRCA 17 1636972 1636972 + Silent SNP G G A TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr17:1636972G>A c.4641G>A c.(4639-4641)ggG>ggA p.G1547G CESC 17 1629218 1629218 + Missense_Mutation SNP A A G TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr17:1629218A>G c.965A>G c.(964-966)gAt>gGt p.D322G CESC 17 1629270 1629270 + Silent SNP C C A TCGA-RA-A741-01A-11D-A33O-09 TCGA-RA-A741-10B-01D-A33O-09 g.chr17:1629270C>A c.1017C>A c.(1015-1017)ccC>ccA p.P339P CESC 17 1629280 1629280 + Nonsense_Mutation SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr17:1629280G>T c.1027G>T c.(1027-1029)Gag>Tag p.E343* CESC 17 1629456 1629456 + Silent SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr17:1629456G>A c.1203G>A c.(1201-1203)aaG>aaA p.K401K CESC 17 1629541 1629541 + Missense_Mutation SNP G G C TCGA-FU-A3TX-01A-11D-A22X-09 TCGA-FU-A3TX-10A-01D-A22X-09 g.chr17:1629541G>C c.1288G>C c.(1288-1290)Ggc>Cgc p.G430R CESC 17 1629718 1629718 + Missense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr17:1629718G>A c.1465G>A c.(1465-1467)Gat>Aat p.D489N CESC 17 1634405 1634405 + Missense_Mutation SNP G G A TCGA-MU-A5YI-01A-11D-A32I-09 TCGA-MU-A5YI-10A-01D-A32I-09 g.chr17:1634405G>A c.4010G>A c.(4009-4011)cGt>cAt p.R1337H CESC 17 1634415 1634415 + Silent SNP G G A TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr17:1634415G>A c.4020G>A c.(4018-4020)gcG>gcA p.A1340A CESC 17 1634540 1634540 + Missense_Mutation SNP C C T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr17:1634540C>T c.4145C>T c.(4144-4146)tCc>tTc p.S1382F CESC 17 1637014 1637014 + Silent SNP C C T TCGA-EK-A2GZ-01A-11D-A17W-09 TCGA-EK-A2GZ-10A-01D-A17W-09 g.chr17:1637014C>T c.4683C>T c.(4681-4683)agC>agT p.S1561S CESC 17 1637052 1637052 + Missense_Mutation SNP C C T TCGA-EA-A78R-01A-11D-A32I-09 TCGA-EA-A78R-10A-01D-A32I-09 g.chr17:1637052C>T c.4721C>T c.(4720-4722)tCt>tTt p.S1574F CESC 17 1639342 1639342 + Nonsense_Mutation SNP C C T TCGA-C5-A1BI-01B-11D-A13W-08 TCGA-C5-A1BI-10A-01D-A13W-08 g.chr17:1639342C>T c.5335C>T c.(5335-5337)Cga>Tga p.R1779* CHOL 17 1628548 1628548 + Missense_Mutation SNP C C T TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr17:1628548C>T c.295C>T c.(295-297)Cct>Tct p.P99S COAD 17 1629654 1629654 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:1629654C>T c.1401C>T c.(1399-1401)gtC>gtT p.V467V COAD 17 1629795 1629795 + Silent SNP G G T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr17:1629795G>T c.1542G>T c.(1540-1542)gtG>gtT p.V514V COAD 17 1630593 1630593 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1630593G>T c.2340G>T c.(2338-2340)gaG>gaT p.E780D COAD 17 1630802 1630802 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr17:1630802C>A c.2549C>A c.(2548-2550)cCt>cAt p.P850H COAD 17 1631119 1631119 + Frame_Shift_Del DEL A A - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:1631119delA c.2866delA c.(2866-2868)aaafs p.K956fs COAD 17 1631568 1631568 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr17:1631568G>A c.3315G>A c.(3313-3315)ctG>ctA p.L1105L COAD 17 1635623 1635623 + Missense_Mutation SNP C C T TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr17:1635623C>T c.4162C>T c.(4162-4164)Cca>Tca p.P1388S COAD 17 1635692 1635692 + Missense_Mutation SNP C C T TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr17:1635692C>T c.4231C>T c.(4231-4233)Cgc>Tgc p.R1411C COAD 17 1635692 1635692 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1635692C>T c.4231C>T c.(4231-4233)Cgc>Tgc p.R1411C COAD 17 1635700 1635700 + Silent SNP A A T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr17:1635700A>T c.4239A>T c.(4237-4239)ggA>ggT p.G1413G COAD 17 1636003 1636003 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:1636003C>A c.4367C>A c.(4366-4368)cCa>cAa p.P1456Q COAD 17 1637429 1637429 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:1637429G>A c.5098G>A c.(5098-5100)Gtc>Atc p.V1700I COAD 17 1638901 1638901 + Missense_Mutation SNP C C T TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr17:1638901C>T c.5215C>T c.(5215-5217)Cgg>Tgg p.R1739W COAD 17 1638935 1638935 + Frame_Shift_Del DEL C C - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:1638935delC c.5249delC c.(5248-5250)gccfs p.A1750fs COAD 17 1639342 1639342 + Nonsense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:1639342C>T c.5335C>T c.(5335-5337)Cga>Tga p.R1779* COAD 17 1639351 1639351 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1639351G>A c.5344G>A c.(5344-5346)Ggt>Agt p.G1782S COAD 17 1640793 1640793 + Silent SNP C C T TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr17:1640793C>T c.5640C>T c.(5638-5640)agC>agT p.S1880S COADREAD 17 1628758 1628758 + Missense_Mutation SNP T T C TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr17:1628758T>C c.505T>C c.(505-507)Tca>Cca p.S169P COADREAD 17 1629654 1629654 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:1629654C>T c.1401C>T c.(1399-1401)gtC>gtT p.V467V COADREAD 17 1629795 1629795 + Silent SNP G G T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr17:1629795G>T c.1542G>T c.(1540-1542)gtG>gtT p.V514V COADREAD 17 1630593 1630593 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1630593G>T c.2340G>T c.(2338-2340)gaG>gaT p.E780D COADREAD 17 1630802 1630802 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr17:1630802C>A c.2549C>A c.(2548-2550)cCt>cAt p.P850H COADREAD 17 1631119 1631119 + Frame_Shift_Del DEL A A - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:1631119delA c.2866delA c.(2866-2868)aaafs p.K956fs COADREAD 17 1631568 1631568 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr17:1631568G>A c.3315G>A c.(3313-3315)ctG>ctA p.L1105L COADREAD 17 1635623 1635623 + Missense_Mutation SNP C C T TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr17:1635623C>T c.4162C>T c.(4162-4164)Cca>Tca p.P1388S COADREAD 17 1635692 1635692 + Missense_Mutation SNP C C T TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr17:1635692C>T c.4231C>T c.(4231-4233)Cgc>Tgc p.R1411C COADREAD 17 1635692 1635692 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1635692C>T c.4231C>T c.(4231-4233)Cgc>Tgc p.R1411C COADREAD 17 1635700 1635700 + Silent SNP A A T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr17:1635700A>T c.4239A>T c.(4237-4239)ggA>ggT p.G1413G COADREAD 17 1636003 1636003 + Missense_Mutation SNP C C A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:1636003C>A c.4367C>A c.(4366-4368)cCa>cAa p.P1456Q COADREAD 17 1637429 1637429 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:1637429G>A c.5098G>A c.(5098-5100)Gtc>Atc p.V1700I COADREAD 17 1638901 1638901 + Missense_Mutation SNP C C T TCGA-CM-6675-01A-11D-1835-10 TCGA-CM-6675-10A-01D-1835-10 g.chr17:1638901C>T c.5215C>T c.(5215-5217)Cgg>Tgg p.R1739W COADREAD 17 1638935 1638935 + Frame_Shift_Del DEL C C - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:1638935delC c.5249delC c.(5248-5250)gccfs p.A1750fs COADREAD 17 1639342 1639342 + Nonsense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:1639342C>T c.5335C>T c.(5335-5337)Cga>Tga p.R1779* COADREAD 17 1639351 1639351 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1639351G>A c.5344G>A c.(5344-5346)Ggt>Agt p.G1782S COADREAD 17 1640793 1640793 + Silent SNP C C T TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr17:1640793C>T c.5640C>T c.(5638-5640)agC>agT p.S1880S DLBC 17 1634183 1634183 + Missense_Mutation SNP C C T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr17:1634183C>T c.3910C>T c.(3910-3912)Cgc>Tgc p.R1304C DLBC 17 1636950 1636950 + Missense_Mutation SNP C C A TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr17:1636950C>A c.4619C>A c.(4618-4620)cCc>cAc p.P1540H ESCA 17 1619894 1619894 + Missense_Mutation SNP C C A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr17:1619894C>A c.25C>A c.(25-27)Ctg>Atg p.L9M ESCA 17 1628919 1628919 + Missense_Mutation SNP G G T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr17:1628919G>T c.666G>T c.(664-666)gaG>gaT p.E222D ESCA 17 1629539 1629539 + Missense_Mutation SNP C C T TCGA-VR-A8EO-01A-11D-A36J-09 TCGA-VR-A8EO-10A-01D-A36M-09 g.chr17:1629539C>T c.1286C>T c.(1285-1287)gCg>gTg p.A429V ESCA 17 1631342 1631343 + Missense_Mutation DNP AG AG CT TCGA-LN-A7HW-01A-22D-A351-09 TCGA-LN-A7HW-10A-01D-A351-09 g.chr17:1631342_1631343AG>CT c.3089_3090AG>CT c.(3088-3090)gAG>gCT p.E1030A ESCA 17 1631464 1631464 + Missense_Mutation SNP G G T TCGA-L5-A4OS-01A-11D-A28B-09 TCGA-L5-A4OS-11A-11D-A28E-09 g.chr17:1631464G>T c.3211G>T c.(3211-3213)Gtc>Ttc p.V1071F ESCA 17 1637131 1637131 + Silent SNP C C T TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr17:1637131C>T c.4800C>T c.(4798-4800)aaC>aaT p.N1600N ESCA 17 1637328 1637328 + Missense_Mutation SNP G G A TCGA-LN-A4A1-01A-21D-A27G-09 TCGA-LN-A4A1-10A-01D-A27G-09 g.chr17:1637328G>A c.4997G>A c.(4996-4998)gGc>gAc p.G1666D ESCA 17 1639332 1639332 + Splice_Site SNP G G T TCGA-IG-A3QL-01A-11D-A247-09 TCGA-IG-A3QL-10A-01D-A247-09 g.chr17:1639332G>T c.e9-1 ESCA 17 1640737 1640737 + Missense_Mutation SNP A A G TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr17:1640737A>G c.5584A>G c.(5584-5586)Acc>Gcc p.T1862A GBM 17 1634533 1634533 + Missense_Mutation SNP C C G TCGA-27-1837-01A-01D-1494-08 TCGA-27-1837-10A-01D-1494-08 g.chr17:1634533C>G c.4138C>G c.(4138-4140)Ctc>Gtc p.L1380V GBMLGG 17 1631740 1631740 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1631740G>A c.3487G>A c.(3487-3489)Gtg>Atg p.V1163M GBMLGG 17 1633762 1633762 + Silent SNP G G A TCGA-VM-A8CH-01A-12D-A36O-08 TCGA-VM-A8CH-10A-01D-A367-08 g.chr17:1633762G>A c.3756G>A c.(3754-3756)ctG>ctA p.L1252L GBMLGG 17 1634379 1634379 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1634379C>A c.3984C>A c.(3982-3984)gcC>gcA p.A1328A GBMLGG 17 1634533 1634533 + Missense_Mutation SNP C C G TCGA-27-1837-01A-01D-1494-08 TCGA-27-1837-10A-01D-1494-08 g.chr17:1634533C>G c.4138C>G c.(4138-4140)Ctc>Gtc p.L1380V GBMLGG 17 1636086 1636086 + Missense_Mutation SNP A A G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chr17:1636086A>G c.4450A>G c.(4450-4452)Atg>Gtg p.M1484V GBMLGG 17 1636832 1636832 + Missense_Mutation SNP C C T TCGA-S9-A6TX-01A-21D-A32B-08 TCGA-S9-A6TX-10A-01D-A329-08 g.chr17:1636832C>T c.4501C>T c.(4501-4503)Cgg>Tgg p.R1501W GBMLGG 17 1636912 1636912 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1636912C>A c.4581C>A c.(4579-4581)aaC>aaA p.N1527K GBMLGG 17 1637326 1637326 + Silent SNP C C T TCGA-IK-7675-01A-11D-2086-08 TCGA-IK-7675-10A-01D-2086-08 g.chr17:1637326C>T c.4995C>T c.(4993-4995)agC>agT p.S1665S GBMLGG 17 1639495 1639495 + Missense_Mutation SNP G G A TCGA-HW-8321-01A-11D-2395-08 TCGA-HW-8321-10A-01D-2396-08 g.chr17:1639495G>A c.5488G>A c.(5488-5490)Gac>Aac p.D1830N GBMLGG 17 1640869 1640869 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1640869A>G c.5716A>G c.(5716-5718)Aag>Gag p.K1906E GBMLGG 17 1640948 1640949 + Frame_Shift_Ins INS - - G TCGA-QH-A6CZ-01A-11D-A32B-08 TCGA-QH-A6CZ-10B-01D-A329-08 g.chr17:1640948_1640949insG c.5795_5796insG c.(5794-5799)tcagacfs p.D1933fs HNSC 17 1634142 1634142 + Missense_Mutation SNP T T G TCGA-H7-8501-01A-11D-2394-08 TCGA-H7-8501-10A-01D-2394-08 g.chr17:1634142T>G c.3869T>G c.(3868-3870)aTc>aGc p.I1290S HNSC 17 1634161 1634161 + Silent SNP C C T TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr17:1634161C>T c.3888C>T c.(3886-3888)ctC>ctT p.L1296L HNSC 17 1634467 1634467 + Missense_Mutation SNP G G A TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr17:1634467G>A c.4072G>A c.(4072-4074)Gac>Aac p.D1358N HNSC 17 1635682 1635682 + Silent SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr17:1635682C>T c.4221C>T c.(4219-4221)ctC>ctT p.L1407L HNSC 17 1636020 1636020 + Missense_Mutation SNP G G A TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr17:1636020G>A c.4384G>A c.(4384-4386)Gat>Aat p.D1462N HNSC 17 1636853 1636853 + Missense_Mutation SNP G G C TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr17:1636853G>C c.4522G>C c.(4522-4524)Gag>Cag p.E1508Q HNSC 17 1639389 1639389 + Silent SNP C C T TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr17:1639389C>T c.5382C>T c.(5380-5382)atC>atT p.I1794I KIPAN 17 1628392 1628392 + Missense_Mutation SNP C C T TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr17:1628392C>T c.139C>T c.(139-141)Ccg>Tcg p.P47S KIPAN 17 1629728 1629728 + Frame_Shift_Del DEL T T - TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr17:1629728delT c.1475delT c.(1474-1476)attfs p.I492fs KIPAN 17 1630052 1630052 + Missense_Mutation SNP C C T TCGA-B1-A47N-01A-11D-A25F-10 TCGA-B1-A47N-10A-01D-A25F-10 g.chr17:1630052C>T c.1799C>T c.(1798-1800)cCc>cTc p.P600L KIPAN 17 1630178 1630178 + Missense_Mutation SNP C C G TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr17:1630178C>G c.1925C>G c.(1924-1926)cCc>cGc p.P642R KIPAN 17 1630298 1630298 + Missense_Mutation SNP C C T TCGA-A4-A57E-01A-11D-A26P-10 TCGA-A4-A57E-10A-01D-A26P-10 g.chr17:1630298C>T c.2045C>T c.(2044-2046)tCc>tTc p.S682F KIPAN 17 1631524 1631524 + Missense_Mutation SNP G G A TCGA-BQ-7062-01A-11D-1961-08 TCGA-BQ-7062-11A-01D-1961-08 g.chr17:1631524G>A c.3271G>A c.(3271-3273)Gtg>Atg p.V1091M KIPAN 17 1633695 1633695 + Missense_Mutation SNP G G T TCGA-B0-4815-01A-01D-1501-10 TCGA-B0-4815-11A-02D-1501-10 g.chr17:1633695G>T c.3689G>T c.(3688-3690)cGc>cTc p.R1230L KIPAN 17 1633711 1633711 + Silent SNP G G A TCGA-A4-8515-01A-11D-2396-08 TCGA-A4-8515-10A-01D-2396-08 g.chr17:1633711G>A c.3705G>A c.(3703-3705)aaG>aaA p.K1235K KIPAN 17 1633775 1633775 + Missense_Mutation SNP T T C TCGA-BP-5009-01A-01D-1462-08 TCGA-BP-5009-11A-01D-1462-08 g.chr17:1633775T>C c.3769T>C c.(3769-3771)Tat>Cat p.Y1257H KIPAN 17 1634093 1634093 + Frame_Shift_Del DEL C C - TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr17:1634093delC c.3820delC c.(3820-3822)ccgfs p.P1274fs KIPAN 17 1634163 1634164 + Frame_Shift_Ins INS - - A TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr17:1634163_1634164insA c.3890_3891insA c.(3889-3894)agctgcfs p.SC1297fs KIPAN 17 1634217 1634217 + Missense_Mutation SNP A A T TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr17:1634217A>T c.3944A>T c.(3943-3945)tAc>tTc p.Y1315F KIPAN 17 1636960 1636960 + Frame_Shift_Del DEL C C - TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr17:1636960delC c.4629delC c.(4627-4629)gacfs p.D1543fs KIRC 17 1633695 1633695 + Missense_Mutation SNP G G T TCGA-B0-4815-01A-01D-1501-10 TCGA-B0-4815-11A-02D-1501-10 g.chr17:1633695G>T c.3689G>T c.(3688-3690)cGc>cTc p.R1230L KIRC 17 1633775 1633775 + Missense_Mutation SNP T T C TCGA-BP-5009-01A-01D-1462-08 TCGA-BP-5009-11A-01D-1462-08 g.chr17:1633775T>C c.3769T>C c.(3769-3771)Tat>Cat p.Y1257H KIRC 17 1634217 1634217 + Missense_Mutation SNP A A T TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr17:1634217A>T c.3944A>T c.(3943-3945)tAc>tTc p.Y1315F KIRC 17 1636960 1636960 + Frame_Shift_Del DEL C C - TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr17:1636960delC c.4629delC c.(4627-4629)gacfs p.D1543fs KIRP 17 1628392 1628392 + Missense_Mutation SNP C C T TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr17:1628392C>T c.139C>T c.(139-141)Ccg>Tcg p.P47S KIRP 17 1629728 1629728 + Frame_Shift_Del DEL T T - TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr17:1629728delT c.1475delT c.(1474-1476)attfs p.I492fs KIRP 17 1630052 1630052 + Missense_Mutation SNP C C T TCGA-B1-A47N-01A-11D-A25F-10 TCGA-B1-A47N-10A-01D-A25F-10 g.chr17:1630052C>T c.1799C>T c.(1798-1800)cCc>cTc p.P600L KIRP 17 1630178 1630178 + Missense_Mutation SNP C C G TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr17:1630178C>G c.1925C>G c.(1924-1926)cCc>cGc p.P642R KIRP 17 1630298 1630298 + Missense_Mutation SNP C C T TCGA-A4-A57E-01A-11D-A26P-10 TCGA-A4-A57E-10A-01D-A26P-10 g.chr17:1630298C>T c.2045C>T c.(2044-2046)tCc>tTc p.S682F KIRP 17 1631524 1631524 + Missense_Mutation SNP G G A TCGA-BQ-7062-01A-11D-1961-08 TCGA-BQ-7062-11A-01D-1961-08 g.chr17:1631524G>A c.3271G>A c.(3271-3273)Gtg>Atg p.V1091M KIRP 17 1633711 1633711 + Silent SNP G G A TCGA-A4-8515-01A-11D-2396-08 TCGA-A4-8515-10A-01D-2396-08 g.chr17:1633711G>A c.3705G>A c.(3703-3705)aaG>aaA p.K1235K KIRP 17 1634093 1634093 + Frame_Shift_Del DEL C C - TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr17:1634093delC c.3820delC c.(3820-3822)ccgfs p.P1274fs KIRP 17 1634163 1634164 + Frame_Shift_Ins INS - - A TCGA-SX-A7SL-01A-11D-A34Z-10 TCGA-SX-A7SL-10A-01D-A34Z-10 g.chr17:1634163_1634164insA c.3890_3891insA c.(3889-3894)agctgcfs p.SC1297fs LGG 17 1631740 1631740 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1631740G>A c.3487G>A c.(3487-3489)Gtg>Atg p.V1163M LGG 17 1633762 1633762 + Silent SNP G G A TCGA-VM-A8CH-01A-12D-A36O-08 TCGA-VM-A8CH-10A-01D-A367-08 g.chr17:1633762G>A c.3756G>A c.(3754-3756)ctG>ctA p.L1252L LGG 17 1634379 1634379 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1634379C>A c.3984C>A c.(3982-3984)gcC>gcA p.A1328A LGG 17 1636086 1636086 + Missense_Mutation SNP A A G TCGA-DU-A5TU-01A-11D-A289-08 TCGA-DU-A5TU-10A-01D-A289-08 g.chr17:1636086A>G c.4450A>G c.(4450-4452)Atg>Gtg p.M1484V LGG 17 1636832 1636832 + Missense_Mutation SNP C C T TCGA-S9-A6TX-01A-21D-A32B-08 TCGA-S9-A6TX-10A-01D-A329-08 g.chr17:1636832C>T c.4501C>T c.(4501-4503)Cgg>Tgg p.R1501W LGG 17 1636912 1636912 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1636912C>A c.4581C>A c.(4579-4581)aaC>aaA p.N1527K LGG 17 1637326 1637326 + Silent SNP C C T TCGA-IK-7675-01A-11D-2086-08 TCGA-IK-7675-10A-01D-2086-08 g.chr17:1637326C>T c.4995C>T c.(4993-4995)agC>agT p.S1665S LGG 17 1639495 1639495 + Missense_Mutation SNP G G A TCGA-HW-8321-01A-11D-2395-08 TCGA-HW-8321-10A-01D-2396-08 g.chr17:1639495G>A c.5488G>A c.(5488-5490)Gac>Aac p.D1830N LGG 17 1640869 1640869 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1640869A>G c.5716A>G c.(5716-5718)Aag>Gag p.K1906E LGG 17 1640948 1640949 + Frame_Shift_Ins INS - - G TCGA-QH-A6CZ-01A-11D-A32B-08 TCGA-QH-A6CZ-10B-01D-A329-08 g.chr17:1640948_1640949insG c.5795_5796insG c.(5794-5799)tcagacfs p.D1933fs LIHC 17 1630159 1630159 + Missense_Mutation SNP C C T TCGA-DD-AADP-01A-11D-A38X-10 TCGA-DD-AADP-10A-01D-A38X-10 g.chr17:1630159C>T c.1906C>T c.(1906-1908)Cca>Tca p.P636S LIHC 17 1630783 1630783 + Nonsense_Mutation SNP C C T TCGA-G3-A5SM-01A-12D-A28X-10 TCGA-G3-A5SM-10A-01D-A28X-10 g.chr17:1630783C>T c.2530C>T c.(2530-2532)Caa>Taa p.Q844* LIHC 17 1634133 1634133 + Missense_Mutation SNP T T C TCGA-DD-A39V-01A-11D-A20W-10 TCGA-DD-A39V-11A-11D-A20W-10 g.chr17:1634133T>C c.3860T>C c.(3859-3861)cTg>cCg p.L1287P LUAD 17 1631425 1631425 + Missense_Mutation SNP G G T TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr17:1631425G>T c.3172G>T c.(3172-3174)Gcc>Tcc p.A1058S LUAD 17 1634230 1634230 + Missense_Mutation SNP C C G TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr17:1634230C>G c.3957C>G c.(3955-3957)atC>atG p.I1319M LUAD 17 1636085 1636085 + Missense_Mutation SNP G G T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr17:1636085G>T c.4449G>T c.(4447-4449)gaG>gaT p.E1483D LUAD 17 1637107 1637107 + Silent SNP C C A TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chr17:1637107C>A c.4776C>A c.(4774-4776)ggC>ggA p.G1592G LUAD 17 1639474 1639474 + Missense_Mutation SNP G G A TCGA-44-A47F-01A-11D-A24D-08 TCGA-44-A47F-10A-01D-A24F-08 g.chr17:1639474G>A c.5467G>A c.(5467-5469)Ggc>Agc p.G1823S LUAD 17 1640811 1640811 + Silent SNP C C T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr17:1640811C>T c.5658C>T c.(5656-5658)acC>acT p.T1886T LUAD 17 1640949 1640949 + Silent SNP A A T TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr17:1640949A>T c.5796A>T c.(5794-5796)tcA>tcT p.S1932S LUAD 17 1640965 1640965 + Missense_Mutation SNP C C T TCGA-50-5044-01A-21D-1855-08 TCGA-50-5044-10A-01D-1855-08 g.chr17:1640965C>T c.5812C>T c.(5812-5814)Cgc>Tgc p.R1938C LUSC 17 1638985 1638985 + Missense_Mutation SNP G G A TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr17:1638985G>A c.5299G>A c.(5299-5301)Gtg>Atg p.V1767M OV 17 1636852 1636852 + Missense_Mutation SNP C C A TCGA-29-2429-01A-01D-1526-09 TCGA-29-2429-10A-01D-1526-09 g.chr17:1636852C>A c.4521C>A c.(4519-4521)caC>caA p.H1507Q PRAD 17 1633695 1633695 + Missense_Mutation SNP G G T TCGA-EJ-5527-01A-01D-1576-08 TCGA-EJ-5527-10A-01D-1577-08 g.chr17:1633695G>T c.3689G>T c.(3688-3690)cGc>cTc p.R1230L PRAD 17 1635978 1635978 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1635978G>A c.4342G>A c.(4342-4344)Gcg>Acg p.A1448T PRAD 17 1637102 1637102 + Frame_Shift_Del DEL G G - TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr17:1637102delG c.4771delG c.(4771-4773)gggfs p.G1592fs PRAD 17 1637344 1637344 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1637344C>T c.5013C>T c.(5011-5013)acC>acT p.T1671T READ 17 1628758 1628758 + Missense_Mutation SNP T T C TCGA-DC-6157-01A-11D-1657-10 TCGA-DC-6157-10A-01D-1657-10 g.chr17:1628758T>C c.505T>C c.(505-507)Tca>Cca p.S169P SARC 17 1630298 1630298 + Missense_Mutation SNP C C T TCGA-DX-A3UF-01A-11D-A307-09 TCGA-DX-A3UF-10A-01D-A307-09 g.chr17:1630298C>T c.2045C>T c.(2044-2046)tCc>tTc p.S682F SARC 17 1630732 1630732 + Nonsense_Mutation SNP C C T TCGA-X6-A8C6-01A-11D-A36J-09 TCGA-X6-A8C6-10A-01D-A36M-09 g.chr17:1630732C>T c.2479C>T c.(2479-2481)Cag>Tag p.Q827* SARC 17 1631292 1631292 + Silent SNP G G A TCGA-WK-A8XX-01A-11D-A37C-09 TCGA-WK-A8XX-10A-01D-A37F-09 g.chr17:1631292G>A c.3039G>A c.(3037-3039)gcG>gcA p.A1013A SKCM 17 1631537 1631537 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr17:1631537C>T c.3284C>T c.(3283-3285)cCc>cTc p.P1095L SKCM 17 1631593 1631593 + Missense_Mutation SNP A A G TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr17:1631593A>G c.3340A>G c.(3340-3342)Acc>Gcc p.T1114A SKCM 17 1631646 1631646 + Silent SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr17:1631646C>T c.3393C>T c.(3391-3393)ccC>ccT p.P1131P SKCM 17 1631701 1631701 + Missense_Mutation SNP G G C TCGA-GN-A268-06A-11D-A196-08 TCGA-GN-A268-10A-01D-A198-08 g.chr17:1631701G>C c.3448G>C c.(3448-3450)Gag>Cag p.E1150Q SKCM 17 1636905 1636905 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr17:1636905G>A c.4574G>A c.(4573-4575)aGt>aAt p.S1525N SKCM 17 1637215 1637215 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:1637215C>T c.4884C>T c.(4882-4884)agC>agT p.S1628S SKCM 17 1637235 1637235 + Missense_Mutation SNP A A T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr17:1637235A>T c.4904A>T c.(4903-4905)cAc>cTc p.H1635L SKCM 17 1637434 1637434 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr17:1637434C>T c.5103C>T c.(5101-5103)ttC>ttT p.F1701F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 17 1617119 1617119 single base substitution T A upstream_gene_variant BLCA-CN 17 1634195 1634195 single base substitution G A 5_prime_UTR_variant BLCA-CN 17 1634195 1634195 single base substitution G A downstream_gene_variant BLCA-CN 17 1634195 1634195 single base substitution G A exon_variant BLCA-CN 17 1634195 1634195 single base substitution G A intron_variant BLCA-CN 17 1634195 1634195 single base substitution G A missense_variant E105K 313G>A BLCA-CN 17 1634195 1634195 single base substitution G A missense_variant E1308K 3922G>A BLCA-CN 17 1634195 1634195 single base substitution G A missense_variant E188K 562G>A BLCA-CN 17 1634195 1634195 single base substitution G A missense_variant E257K 769G>A BLCA-CN 17 1634195 1634195 single base substitution G A missense_variant E81K 241G>A BLCA-CN 17 1634195 1634195 single base substitution G A synonymous_variant G2G 6G>A BLCA-CN 17 1634195 1634195 single base substitution G A upstream_gene_variant BLCA-CN 17 1636934 1636934 single base substitution A G downstream_gene_variant BLCA-CN 17 1636934 1636934 single base substitution A G exon_variant BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M120V 358A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M1535V 4603A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M166V 496A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M170V 508A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M174V 520A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M308V 922A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M332V 994A>G BLCA-CN 17 1636934 1636934 single base substitution A G missense_variant M484V 1450A>G BLCA-US 17 1639411 1639411 single base substitution G A downstream_gene_variant BLCA-US 17 1639411 1639411 single base substitution G A exon_variant BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V1802M 5404G>A BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V433M 1297G>A BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V441M 1321G>A BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V575M 1723G>A BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V599M 1795G>A BLCA-US 17 1639411 1639411 single base substitution G A missense_variant V751M 2251G>A BLCA-US 17 1640893 1640893 single base substitution G A downstream_gene_variant BLCA-US 17 1640893 1640893 single base substitution G A exon_variant BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G1914S 5740G>A BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G545S 1633G>A BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G553S 1657G>A BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G687S 2059G>A BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G711S 2131G>A BLCA-US 17 1640893 1640893 single base substitution G A missense_variant G863S 2587G>A BRCA-EU 17 1615300 1615300 single base substitution A C upstream_gene_variant BRCA-EU 17 1615832 1615832 single base substitution C T upstream_gene_variant BRCA-EU 17 1616612 1616612 single base substitution C A upstream_gene_variant BRCA-EU 17 1617388 1617388 single base substitution G T upstream_gene_variant BRCA-EU 17 1618300 1618300 single base substitution C G upstream_gene_variant BRCA-EU 17 1623456 1623456 single base substitution C T intron_variant BRCA-EU 17 1623456 1623456 single base substitution C T upstream_gene_variant BRCA-EU 17 1626804 1626804 single base substitution G A intron_variant BRCA-EU 17 1626804 1626804 single base substitution G A upstream_gene_variant BRCA-EU 17 1628881 1628881 single base substitution C T intron_variant BRCA-EU 17 1628881 1628881 single base substitution C T missense_variant R210W 628C>T BRCA-EU 17 1628881 1628881 single base substitution C T upstream_gene_variant BRCA-EU 17 1629600 1629600 single base substitution G A intron_variant BRCA-EU 17 1629600 1629600 single base substitution G A synonymous_variant T449T 1347G>A BRCA-EU 17 1629600 1629600 single base substitution G A upstream_gene_variant BRCA-EU 17 1629652 1629652 single base substitution G A intron_variant BRCA-EU 17 1629652 1629652 single base substitution G A missense_variant V467I 1399G>A BRCA-EU 17 1629652 1629652 single base substitution G A upstream_gene_variant BRCA-EU 17 1631075 1631075 single base substitution C T exon_variant BRCA-EU 17 1631075 1631075 single base substitution C T intron_variant BRCA-EU 17 1631075 1631075 single base substitution C T missense_variant T941M 2822C>T BRCA-EU 17 1631075 1631075 single base substitution C T upstream_gene_variant BRCA-EU 17 1631891 1631891 single base substitution C G exon_variant BRCA-EU 17 1631891 1631891 single base substitution C G intron_variant BRCA-EU 17 1631891 1631891 single base substitution C G stop_gained S1213* 3638C>G BRCA-EU 17 1631891 1631891 single base substitution C G stop_gained S129* 386C>G BRCA-EU 17 1631891 1631891 single base substitution C G stop_gained S162* 485C>G BRCA-EU 17 1631891 1631891 single base substitution C G upstream_gene_variant BRCA-EU 17 1632538 1632538 single base substitution C T intron_variant BRCA-EU 17 1632538 1632538 single base substitution C T upstream_gene_variant BRCA-EU 17 1633181 1633181 single base substitution G A intron_variant BRCA-EU 17 1633181 1633181 single base substitution G A upstream_gene_variant BRCA-EU 17 1638550 1638550 single base substitution C T downstream_gene_variant BRCA-EU 17 1638550 1638550 single base substitution C T intron_variant BRCA-EU 17 1642946 1642946 single base substitution A G downstream_gene_variant BRCA-EU 17 1644024 1644024 single base substitution G A downstream_gene_variant BRCA-EU 17 1644681 1644681 single base substitution T C downstream_gene_variant BRCA-EU 17 1646119 1646119 single base substitution G T downstream_gene_variant BRCA-EU 17 1646120 1646120 single base substitution C T downstream_gene_variant BRCA-EU 17 1646808 1646808 single base substitution G A downstream_gene_variant BRCA-FR 17 1615832 1615832 single base substitution C T upstream_gene_variant BRCA-FR 17 1618300 1618300 single base substitution C G upstream_gene_variant BRCA-FR 17 1624176 1624176 single base substitution T C intron_variant BRCA-FR 17 1624176 1624176 single base substitution T C upstream_gene_variant BRCA-FR 17 1632196 1632196 single base substitution G C intron_variant BRCA-FR 17 1632196 1632196 single base substitution G C upstream_gene_variant BRCA-FR 17 1633157 1633157 single base substitution G A intron_variant BRCA-FR 17 1633157 1633157 single base substitution G A upstream_gene_variant BRCA-FR 17 1638550 1638550 single base substitution C T downstream_gene_variant BRCA-FR 17 1638550 1638550 single base substitution C T intron_variant BRCA-UK 17 1643756 1643756 single base substitution A C downstream_gene_variant BRCA-US 17 1628873 1628873 insertion of <=200bp - C frameshift_variant C207S? BRCA-US 17 1628873 1628873 insertion of <=200bp - C intron_variant BRCA-US 17 1628873 1628873 insertion of <=200bp - C upstream_gene_variant BRCA-US 17 1630415 1630415 single base substitution T G intron_variant BRCA-US 17 1630415 1630415 single base substitution T G missense_variant L721R 2162T>G BRCA-US 17 1630415 1630415 single base substitution T G upstream_gene_variant BRCA-US 17 1630714 1630714 single base substitution G A intron_variant BRCA-US 17 1630714 1630714 single base substitution G A missense_variant V821M 2461G>A BRCA-US 17 1630714 1630714 single base substitution G A upstream_gene_variant BRCA-US 17 1636026 1636026 single base substitution C G 3_prime_UTR_variant BRCA-US 17 1636026 1636026 single base substitution C G downstream_gene_variant BRCA-US 17 1636026 1636026 single base substitution C G exon_variant BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q103E 307C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q1464E 4390C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q237E 709C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q261E 781C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q413E 1237C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q49E 145C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q95E 283C>G BRCA-US 17 1636026 1636026 single base substitution C G missense_variant Q99E 295C>G BRCA-US 17 1636972 1636972 single base substitution G A downstream_gene_variant BRCA-US 17 1636972 1636972 single base substitution G A exon_variant BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G132G 396G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G1547G 4641G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G178G 534G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G186G 558G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G320G 960G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G344G 1032G>A BRCA-US 17 1636972 1636972 single base substitution G A synonymous_variant G496G 1488G>A BTCA-JP 17 1631149 1631149 single base substitution C T exon_variant BTCA-JP 17 1631149 1631149 single base substitution C T intron_variant BTCA-JP 17 1631149 1631149 single base substitution C T missense_variant L966F 2896C>T BTCA-JP 17 1631149 1631149 single base substitution C T upstream_gene_variant BTCA-JP 17 1636841 1636841 single base substitution A G downstream_gene_variant BTCA-JP 17 1636841 1636841 single base substitution A G exon_variant BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I135V 403A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I139V 415A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I143V 427A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I1504V 4510A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I277V 829A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I301V 901A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I453V 1357A>G BTCA-JP 17 1636841 1636841 single base substitution A G missense_variant I89V 265A>G CESC-US 17 1616845 1616845 single base substitution C T upstream_gene_variant CESC-US 17 1629218 1629218 single base substitution A G intron_variant CESC-US 17 1629218 1629218 single base substitution A G missense_variant D322G 965A>G CESC-US 17 1629218 1629218 single base substitution A G upstream_gene_variant CESC-US 17 1629270 1629270 single base substitution C A intron_variant CESC-US 17 1629270 1629270 single base substitution C A synonymous_variant P339P 1017C>A CESC-US 17 1629270 1629270 single base substitution C A upstream_gene_variant CESC-US 17 1629280 1629280 single base substitution G T intron_variant CESC-US 17 1629280 1629280 single base substitution G T stop_gained E343* 1027G>T CESC-US 17 1629280 1629280 single base substitution G T upstream_gene_variant CESC-US 17 1629456 1629456 single base substitution G A intron_variant CESC-US 17 1629456 1629456 single base substitution G A synonymous_variant K401K 1203G>A CESC-US 17 1629456 1629456 single base substitution G A upstream_gene_variant CESC-US 17 1629541 1629541 single base substitution G C intron_variant CESC-US 17 1629541 1629541 single base substitution G C missense_variant G430R 1288G>C CESC-US 17 1629541 1629541 single base substitution G C upstream_gene_variant CESC-US 17 1629718 1629718 single base substitution G A intron_variant CESC-US 17 1629718 1629718 single base substitution G A missense_variant D489N 1465G>A CESC-US 17 1629718 1629718 single base substitution G A upstream_gene_variant CESC-US 17 1634405 1634405 single base substitution G A 5_prime_UTR_variant CESC-US 17 1634405 1634405 single base substitution G A downstream_gene_variant CESC-US 17 1634405 1634405 single base substitution G A exon_variant CESC-US 17 1634405 1634405 single base substitution G A intron_variant CESC-US 17 1634405 1634405 single base substitution G A missense_variant R110H 329G>A CESC-US 17 1634405 1634405 single base substitution G A missense_variant R1337H 4010G>A CESC-US 17 1634405 1634405 single base substitution G A missense_variant R134H 401G>A CESC-US 17 1634405 1634405 single base substitution G A missense_variant R286H 857G>A CESC-US 17 1634405 1634405 single base substitution G A upstream_gene_variant CESC-US 17 1634415 1634415 single base substitution G A 5_prime_UTR_variant CESC-US 17 1634415 1634415 single base substitution G A downstream_gene_variant CESC-US 17 1634415 1634415 single base substitution G A exon_variant CESC-US 17 1634415 1634415 single base substitution G A intron_variant CESC-US 17 1634415 1634415 single base substitution G A synonymous_variant A113A 339G>A CESC-US 17 1634415 1634415 single base substitution G A synonymous_variant A1340A 4020G>A CESC-US 17 1634415 1634415 single base substitution G A synonymous_variant A137A 411G>A CESC-US 17 1634415 1634415 single base substitution G A synonymous_variant A289A 867G>A CESC-US 17 1634415 1634415 single base substitution G A upstream_gene_variant CESC-US 17 1634540 1634540 single base substitution C T downstream_gene_variant CESC-US 17 1634540 1634540 single base substitution C T exon_variant CESC-US 17 1634540 1634540 single base substitution C T intron_variant CESC-US 17 1634540 1634540 single base substitution C T missense_variant S1382F 4145C>T CESC-US 17 1634540 1634540 single base substitution C T missense_variant S155F 464C>T CESC-US 17 1634540 1634540 single base substitution C T missense_variant S179F 536C>T CESC-US 17 1634540 1634540 single base substitution C T missense_variant S21F 62C>T CESC-US 17 1634540 1634540 single base substitution C T missense_variant S331F 992C>T CESC-US 17 1637014 1637014 single base substitution C T downstream_gene_variant CESC-US 17 1637014 1637014 single base substitution C T exon_variant CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S1561S 4683C>T CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S192S 576C>T CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S200S 600C>T CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S334S 1002C>T CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S358S 1074C>T CESC-US 17 1637014 1637014 single base substitution C T synonymous_variant S510S 1530C>T CESC-US 17 1637052 1637052 single base substitution C T downstream_gene_variant CESC-US 17 1637052 1637052 single base substitution C T exon_variant CESC-US 17 1637052 1637052 single base substitution C T missense_variant S1574F 4721C>T CESC-US 17 1637052 1637052 single base substitution C T missense_variant S205F 614C>T CESC-US 17 1637052 1637052 single base substitution C T missense_variant S213F 638C>T CESC-US 17 1637052 1637052 single base substitution C T missense_variant S347F 1040C>T CESC-US 17 1637052 1637052 single base substitution C T missense_variant S371F 1112C>T CESC-US 17 1637052 1637052 single base substitution C T missense_variant S523F 1568C>T CESC-US 17 1639342 1639342 single base substitution C T downstream_gene_variant CESC-US 17 1639342 1639342 single base substitution C T exon_variant CESC-US 17 1639342 1639342 single base substitution C T stop_gained R1779* 5335C>T CESC-US 17 1639342 1639342 single base substitution C T stop_gained R410* 1228C>T CESC-US 17 1639342 1639342 single base substitution C T stop_gained R418* 1252C>T CESC-US 17 1639342 1639342 single base substitution C T stop_gained R552* 1654C>T CESC-US 17 1639342 1639342 single base substitution C T stop_gained R576* 1726C>T CESC-US 17 1639342 1639342 single base substitution C T stop_gained R728* 2182C>T CESC-US 17 1641656 1641656 single base substitution G C 3_prime_UTR_variant CESC-US 17 1641656 1641656 single base substitution G C downstream_gene_variant CESC-US 17 1641656 1641656 single base substitution G C exon_variant CESC-US 17 1641719 1641719 single base substitution G C 3_prime_UTR_variant CESC-US 17 1641719 1641719 single base substitution G C downstream_gene_variant CESC-US 17 1641719 1641719 single base substitution G C exon_variant CESC-US 17 1641739 1641739 single base substitution C G 3_prime_UTR_variant CESC-US 17 1641739 1641739 single base substitution C G downstream_gene_variant CESC-US 17 1641739 1641739 single base substitution C G exon_variant CESC-US 17 1641793 1641793 single base substitution G C 3_prime_UTR_variant CESC-US 17 1641793 1641793 single base substitution G C downstream_gene_variant CESC-US 17 1641793 1641793 single base substitution G C exon_variant CLLE-ES 17 1626760 1626760 insertion of <=200bp - TT intron_variant CLLE-ES 17 1626760 1626760 insertion of <=200bp - TT upstream_gene_variant CLLE-ES 17 1643831 1643831 single base substitution C T downstream_gene_variant COAD-US 17 1628274 1628274 single base substitution G T intron_variant COAD-US 17 1628274 1628274 single base substitution G T synonymous_variant G7G 21G>T COAD-US 17 1628274 1628274 single base substitution G T upstream_gene_variant COAD-US 17 1629654 1629654 single base substitution C T intron_variant COAD-US 17 1629654 1629654 single base substitution C T synonymous_variant V467V 1401C>T COAD-US 17 1629654 1629654 single base substitution C T upstream_gene_variant COAD-US 17 1629795 1629795 single base substitution G T intron_variant COAD-US 17 1629795 1629795 single base substitution G T synonymous_variant V514V 1542G>T COAD-US 17 1629795 1629795 single base substitution G T upstream_gene_variant COAD-US 17 1630802 1630802 single base substitution C A intron_variant COAD-US 17 1630802 1630802 single base substitution C A missense_variant P850H 2549C>A COAD-US 17 1630802 1630802 single base substitution C A upstream_gene_variant COAD-US 17 1630992 1630992 single base substitution G A exon_variant COAD-US 17 1630992 1630992 single base substitution G A intron_variant COAD-US 17 1630992 1630992 single base substitution G A synonymous_variant L913L 2739G>A COAD-US 17 1630992 1630992 single base substitution G A upstream_gene_variant COAD-US 17 1631341 1631343 deletion of <=200bp GAG - 5_prime_UTR_variant COAD-US 17 1631341 1631343 deletion of <=200bp GAG - exon_variant COAD-US 17 1631341 1631343 deletion of <=200bp GAG - inframe_deletion E1030 COAD-US 17 1631341 1631343 deletion of <=200bp GAG - intron_variant COAD-US 17 1631341 1631343 deletion of <=200bp GAG - upstream_gene_variant COAD-US 17 1634052 1634052 single base substitution C A 5_prime_UTR_variant COAD-US 17 1634052 1634052 single base substitution C A exon_variant COAD-US 17 1634052 1634052 single base substitution C A intron_variant COAD-US 17 1634052 1634052 single base substitution C A missense_variant P1260H 3779C>A COAD-US 17 1634052 1634052 single base substitution C A missense_variant P140H 419C>A COAD-US 17 1634052 1634052 single base substitution C A missense_variant P209H 626C>A COAD-US 17 1634052 1634052 single base substitution C A missense_variant P33H 98C>A COAD-US 17 1634052 1634052 single base substitution C A missense_variant P57H 170C>A COAD-US 17 1634052 1634052 single base substitution C A upstream_gene_variant COAD-US 17 1635623 1635623 single base substitution C T 5_prime_UTR_variant COAD-US 17 1635623 1635623 single base substitution C T downstream_gene_variant COAD-US 17 1635623 1635623 single base substitution C T exon_variant COAD-US 17 1635623 1635623 single base substitution C T missense_variant P1388S 4162C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P161S 481C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P185S 553C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P19S 55C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P23S 67C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P27S 79C>T COAD-US 17 1635623 1635623 single base substitution C T missense_variant P337S 1009C>T COAD-US 17 1635692 1635692 single base substitution C T 5_prime_UTR_variant COAD-US 17 1635692 1635692 single base substitution C T downstream_gene_variant COAD-US 17 1635692 1635692 single base substitution C T exon_variant COAD-US 17 1635692 1635692 single base substitution C T missense_variant R1411C 4231C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R184C 550C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R208C 622C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R360C 1078C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R42C 124C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R46C 136C>T COAD-US 17 1635692 1635692 single base substitution C T missense_variant R50C 148C>T COAD-US 17 1635700 1635700 single base substitution A T 5_prime_UTR_variant COAD-US 17 1635700 1635700 single base substitution A T downstream_gene_variant COAD-US 17 1635700 1635700 single base substitution A T exon_variant COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G1413G 4239A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G186G 558A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G210G 630A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G362G 1086A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G44G 132A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G48G 144A>T COAD-US 17 1635700 1635700 single base substitution A T synonymous_variant G52G 156A>T COAD-US 17 1636950 1636950 single base substitution C A downstream_gene_variant COAD-US 17 1636950 1636950 single base substitution C A exon_variant COAD-US 17 1636950 1636950 single base substitution C A missense_variant P125H 374C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P1540H 4619C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P171H 512C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P179H 536C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P313H 938C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P337H 1010C>A COAD-US 17 1636950 1636950 single base substitution C A missense_variant P489H 1466C>A COAD-US 17 1637302 1637302 single base substitution A G downstream_gene_variant COAD-US 17 1637302 1637302 single base substitution A G exon_variant COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L1657L 4971A>G COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L288L 864A>G COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L296L 888A>G COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L430L 1290A>G COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L454L 1362A>G COAD-US 17 1637302 1637302 single base substitution A G synonymous_variant L606L 1818A>G COAD-US 17 1637429 1637429 single base substitution G A downstream_gene_variant COAD-US 17 1637429 1637429 single base substitution G A exon_variant COAD-US 17 1637429 1637429 single base substitution G A missense_variant V1700I 5098G>A COAD-US 17 1637429 1637429 single base substitution G A missense_variant V331I 991G>A COAD-US 17 1637429 1637429 single base substitution G A missense_variant V339I 1015G>A COAD-US 17 1637429 1637429 single base substitution G A missense_variant V473I 1417G>A COAD-US 17 1637429 1637429 single base substitution G A missense_variant V497I 1489G>A COAD-US 17 1637429 1637429 single base substitution G A missense_variant V649I 1945G>A COAD-US 17 1637458 1637458 single base substitution G A downstream_gene_variant COAD-US 17 1637458 1637458 single base substitution G A exon_variant COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P1709P 5127G>A COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P340P 1020G>A COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P348P 1044G>A COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P482P 1446G>A COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P506P 1518G>A COAD-US 17 1637458 1637458 single base substitution G A synonymous_variant P658P 1974G>A COAD-US 17 1638901 1638901 single base substitution C T downstream_gene_variant COAD-US 17 1638901 1638901 single base substitution C T exon_variant COAD-US 17 1638901 1638901 single base substitution C T missense_variant R1739W 5215C>T COAD-US 17 1638901 1638901 single base substitution C T missense_variant R370W 1108C>T COAD-US 17 1638901 1638901 single base substitution C T missense_variant R378W 1132C>T COAD-US 17 1638901 1638901 single base substitution C T missense_variant R512W 1534C>T COAD-US 17 1638901 1638901 single base substitution C T missense_variant R536W 1606C>T COAD-US 17 1638901 1638901 single base substitution C T missense_variant R688W 2062C>T COAD-US 17 1638935 1638935 deletion of <=200bp C - downstream_gene_variant COAD-US 17 1638935 1638935 deletion of <=200bp C - exon_variant COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A1750 COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A381 COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A389 COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A523 COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A547 COAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A699 COAD-US 17 1639342 1639342 single base substitution C T downstream_gene_variant COAD-US 17 1639342 1639342 single base substitution C T exon_variant COAD-US 17 1639342 1639342 single base substitution C T stop_gained R1779* 5335C>T COAD-US 17 1639342 1639342 single base substitution C T stop_gained R410* 1228C>T COAD-US 17 1639342 1639342 single base substitution C T stop_gained R418* 1252C>T COAD-US 17 1639342 1639342 single base substitution C T stop_gained R552* 1654C>T COAD-US 17 1639342 1639342 single base substitution C T stop_gained R576* 1726C>T COAD-US 17 1639342 1639342 single base substitution C T stop_gained R728* 2182C>T COAD-US 17 1639351 1639351 single base substitution G A downstream_gene_variant COAD-US 17 1639351 1639351 single base substitution G A exon_variant COAD-US 17 1639351 1639351 single base substitution G A missense_variant G1782S 5344G>A COAD-US 17 1639351 1639351 single base substitution G A missense_variant G413S 1237G>A COAD-US 17 1639351 1639351 single base substitution G A missense_variant G421S 1261G>A COAD-US 17 1639351 1639351 single base substitution G A missense_variant G555S 1663G>A COAD-US 17 1639351 1639351 single base substitution G A missense_variant G579S 1735G>A COAD-US 17 1639351 1639351 single base substitution G A missense_variant G731S 2191G>A COAD-US 17 1639403 1639403 single base substitution G A downstream_gene_variant COAD-US 17 1639403 1639403 single base substitution G A exon_variant COAD-US 17 1639403 1639403 single base substitution G A missense_variant R1799H 5396G>A COAD-US 17 1639403 1639403 single base substitution G A missense_variant R430H 1289G>A COAD-US 17 1639403 1639403 single base substitution G A missense_variant R438H 1313G>A COAD-US 17 1639403 1639403 single base substitution G A missense_variant R572H 1715G>A COAD-US 17 1639403 1639403 single base substitution G A missense_variant R596H 1787G>A COAD-US 17 1639403 1639403 single base substitution G A missense_variant R748H 2243G>A COAD-US 17 1639458 1639458 single base substitution A G downstream_gene_variant COAD-US 17 1639458 1639458 single base substitution A G exon_variant COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T1817T 5451A>G COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T448T 1344A>G COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T456T 1368A>G COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T590T 1770A>G COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T614T 1842A>G COAD-US 17 1639458 1639458 single base substitution A G synonymous_variant T766T 2298A>G COAD-US 17 1640793 1640793 single base substitution C T downstream_gene_variant COAD-US 17 1640793 1640793 single base substitution C T exon_variant COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S1880S 5640C>T COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S511S 1533C>T COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S519S 1557C>T COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S653S 1959C>T COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S677S 2031C>T COAD-US 17 1640793 1640793 single base substitution C T synonymous_variant S829S 2487C>T COCA-CN 17 1616912 1616912 single base substitution G T upstream_gene_variant COCA-CN 17 1619924 1619924 single base substitution C A 5_prime_UTR_variant COCA-CN 17 1619924 1619924 single base substitution C A exon_variant COCA-CN 17 1619924 1619924 single base substitution C A missense_variant A20D 59C>A COCA-CN 17 1619924 1619924 single base substitution C A missense_variant L19I 55C>A COCA-CN 17 1628987 1628987 single base substitution T C intron_variant COCA-CN 17 1628987 1628987 single base substitution T C missense_variant V245A 734T>C COCA-CN 17 1628987 1628987 single base substitution T C upstream_gene_variant COCA-CN 17 1629405 1629405 single base substitution C A intron_variant COCA-CN 17 1629405 1629405 single base substitution C A synonymous_variant P384P 1152C>A COCA-CN 17 1629405 1629405 single base substitution C A upstream_gene_variant COCA-CN 17 1629644 1629644 single base substitution G A intron_variant COCA-CN 17 1629644 1629644 single base substitution G A missense_variant C464Y 1391G>A COCA-CN 17 1629644 1629644 single base substitution G A upstream_gene_variant COCA-CN 17 1630105 1630105 single base substitution G A intron_variant COCA-CN 17 1630105 1630105 single base substitution G A missense_variant G618S 1852G>A COCA-CN 17 1630105 1630105 single base substitution G A upstream_gene_variant COCA-CN 17 1630615 1630615 single base substitution C T intron_variant COCA-CN 17 1630615 1630615 single base substitution C T missense_variant R788W 2362C>T COCA-CN 17 1630615 1630615 single base substitution C T upstream_gene_variant COCA-CN 17 1635614 1635614 single base substitution T C downstream_gene_variant COCA-CN 17 1635614 1635614 single base substitution T C splice_region_variant COCA-CN 17 1636784 1636784 single base substitution T C downstream_gene_variant COCA-CN 17 1636784 1636784 single base substitution T C intron_variant COCA-CN 17 1637331 1637331 single base substitution G A downstream_gene_variant COCA-CN 17 1637331 1637331 single base substitution G A exon_variant COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S1667N 5000G>A COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S298N 893G>A COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S306N 917G>A COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S440N 1319G>A COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S464N 1391G>A COCA-CN 17 1637331 1637331 single base substitution G A missense_variant S616N 1847G>A COCA-CN 17 1637579 1637579 single base substitution C T downstream_gene_variant COCA-CN 17 1637579 1637579 single base substitution C T intron_variant COCA-CN 17 1642727 1642727 single base substitution C T downstream_gene_variant COCA-CN 17 1642743 1642743 single base substitution T C downstream_gene_variant COCA-CN 17 1642817 1642817 single base substitution G C downstream_gene_variant EOPC-DE 17 1643756 1643756 single base substitution A C downstream_gene_variant EOPC-DE 17 1646101 1646101 single base substitution A G downstream_gene_variant ESAD-UK 17 1618023 1618023 single base substitution T A upstream_gene_variant ESAD-UK 17 1622855 1622855 single base substitution A C intron_variant ESAD-UK 17 1622855 1622855 single base substitution A C upstream_gene_variant ESAD-UK 17 1624238 1624238 single base substitution G A intron_variant ESAD-UK 17 1624238 1624238 single base substitution G A upstream_gene_variant ESAD-UK 17 1627092 1627092 single base substitution A T intron_variant ESAD-UK 17 1627092 1627092 single base substitution A T upstream_gene_variant ESAD-UK 17 1629660 1629660 single base substitution G A intron_variant ESAD-UK 17 1629660 1629660 single base substitution G A synonymous_variant A469A 1407G>A ESAD-UK 17 1629660 1629660 single base substitution G A upstream_gene_variant ESAD-UK 17 1636634 1636634 single base substitution G T downstream_gene_variant ESAD-UK 17 1636634 1636634 single base substitution G T intron_variant ESAD-UK 17 1637020 1637020 single base substitution G C downstream_gene_variant ESAD-UK 17 1637020 1637020 single base substitution G C exon_variant ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L1563L 4689G>C ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L194L 582G>C ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L202L 606G>C ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L336L 1008G>C ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L360L 1080G>C ESAD-UK 17 1637020 1637020 single base substitution G C synonymous_variant L512L 1536G>C ESAD-UK 17 1639491 1639491 single base substitution G C downstream_gene_variant ESAD-UK 17 1639491 1639491 single base substitution G C exon_variant ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E1828D 5484G>C ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E459D 1377G>C ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E467D 1401G>C ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E601D 1803G>C ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E625D 1875G>C ESAD-UK 17 1639491 1639491 single base substitution G C missense_variant E777D 2331G>C ESAD-UK 17 1640576 1640576 single base substitution C T downstream_gene_variant ESAD-UK 17 1640576 1640576 single base substitution C T intron_variant ESAD-UK 17 1645722 1645722 single base substitution G C downstream_gene_variant ESAD-UK 17 1646166 1646166 single base substitution G C downstream_gene_variant ESAD-UK 17 1646209 1646209 single base substitution G A downstream_gene_variant ESAD-UK 17 1646214 1646214 insertion of <=200bp - C downstream_gene_variant ESAD-UK 17 1646789 1646789 single base substitution C A downstream_gene_variant ESCA-CN 17 1631913 1631913 single base substitution C T exon_variant ESCA-CN 17 1631913 1631913 single base substitution C T intron_variant ESCA-CN 17 1631913 1631913 single base substitution C T synonymous_variant I1220I 3660C>T ESCA-CN 17 1631913 1631913 single base substitution C T synonymous_variant I136I 408C>T ESCA-CN 17 1631913 1631913 single base substitution C T synonymous_variant I169I 507C>T ESCA-CN 17 1631913 1631913 single base substitution C T upstream_gene_variant ESCA-CN 17 1640761 1640761 single base substitution G A downstream_gene_variant ESCA-CN 17 1640761 1640761 single base substitution G A exon_variant ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D1870N 5608G>A ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D501N 1501G>A ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D509N 1525G>A ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D643N 1927G>A ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D667N 1999G>A ESCA-CN 17 1640761 1640761 single base substitution G A missense_variant D819N 2455G>A GBM-US 17 1634533 1634533 single base substitution C G downstream_gene_variant GBM-US 17 1634533 1634533 single base substitution C G exon_variant GBM-US 17 1634533 1634533 single base substitution C G intron_variant GBM-US 17 1634533 1634533 single base substitution C G missense_variant L1380V 4138C>G GBM-US 17 1634533 1634533 single base substitution C G missense_variant L153V 457C>G GBM-US 17 1634533 1634533 single base substitution C G missense_variant L177V 529C>G GBM-US 17 1634533 1634533 single base substitution C G missense_variant L19V 55C>G GBM-US 17 1634533 1634533 single base substitution C G missense_variant L329V 985C>G KIRC-US 17 1617206 1617206 single base substitution C A upstream_gene_variant KIRC-US 17 1633695 1633695 single base substitution G T exon_variant KIRC-US 17 1633695 1633695 single base substitution G T intron_variant KIRC-US 17 1633695 1633695 single base substitution G T missense_variant R1230L 3689G>T KIRC-US 17 1633695 1633695 single base substitution G T missense_variant R179L 536G>T KIRC-US 17 1633695 1633695 single base substitution G T missense_variant R27L 80G>T KIRC-US 17 1633695 1633695 single base substitution G T missense_variant R3L 8G>T KIRC-US 17 1633695 1633695 single base substitution G T upstream_gene_variant KIRC-US 17 1633775 1633775 single base substitution T C 5_prime_UTR_variant KIRC-US 17 1633775 1633775 single base substitution T C exon_variant KIRC-US 17 1633775 1633775 single base substitution T C intron_variant KIRC-US 17 1633775 1633775 single base substitution T C missense_variant Y1257H 3769T>C KIRC-US 17 1633775 1633775 single base substitution T C missense_variant Y206H 616T>C KIRC-US 17 1633775 1633775 single base substitution T C missense_variant Y30H 88T>C KIRC-US 17 1633775 1633775 single base substitution T C missense_variant Y54H 160T>C KIRC-US 17 1633775 1633775 single base substitution T C upstream_gene_variant KIRC-US 17 1634217 1634217 single base substitution A T 5_prime_UTR_variant KIRC-US 17 1634217 1634217 single base substitution A T downstream_gene_variant KIRC-US 17 1634217 1634217 single base substitution A T exon_variant KIRC-US 17 1634217 1634217 single base substitution A T intron_variant KIRC-US 17 1634217 1634217 single base substitution A T missense_variant T10S 28A>T KIRC-US 17 1634217 1634217 single base substitution A T missense_variant Y112F 335A>T KIRC-US 17 1634217 1634217 single base substitution A T missense_variant Y1315F 3944A>T KIRC-US 17 1634217 1634217 single base substitution A T missense_variant Y195F 584A>T KIRC-US 17 1634217 1634217 single base substitution A T missense_variant Y264F 791A>T KIRC-US 17 1634217 1634217 single base substitution A T missense_variant Y88F 263A>T KIRC-US 17 1634217 1634217 single base substitution A T upstream_gene_variant KIRC-US 17 1636960 1636960 deletion of <=200bp C - downstream_gene_variant KIRC-US 17 1636960 1636960 deletion of <=200bp C - exon_variant KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D128 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D1543 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D174 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D182 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D316 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D340 KIRC-US 17 1636960 1636960 deletion of <=200bp C - frameshift_variant D492 KIRP-US 17 1630052 1630052 single base substitution C T intron_variant KIRP-US 17 1630052 1630052 single base substitution C T missense_variant P600L 1799C>T KIRP-US 17 1630052 1630052 single base substitution C T upstream_gene_variant KIRP-US 17 1630178 1630178 single base substitution C G intron_variant KIRP-US 17 1630178 1630178 single base substitution C G missense_variant P642R 1925C>G KIRP-US 17 1630178 1630178 single base substitution C G upstream_gene_variant KIRP-US 17 1630298 1630298 single base substitution C T intron_variant KIRP-US 17 1630298 1630298 single base substitution C T missense_variant S682F 2045C>T KIRP-US 17 1630298 1630298 single base substitution C T upstream_gene_variant KIRP-US 17 1633711 1633711 single base substitution G A exon_variant KIRP-US 17 1633711 1633711 single base substitution G A intron_variant KIRP-US 17 1633711 1633711 single base substitution G A synonymous_variant K1235K 3705G>A KIRP-US 17 1633711 1633711 single base substitution G A synonymous_variant K184K 552G>A KIRP-US 17 1633711 1633711 single base substitution G A synonymous_variant K32K 96G>A KIRP-US 17 1633711 1633711 single base substitution G A synonymous_variant K8K 24G>A KIRP-US 17 1633711 1633711 single base substitution G A upstream_gene_variant LAML-KR 17 1622610 1622610 single base substitution G A intron_variant LAML-KR 17 1631781 1631781 single base substitution C A exon_variant LAML-KR 17 1631781 1631781 single base substitution C A intron_variant LAML-KR 17 1631781 1631781 single base substitution C A synonymous_variant T1176T 3528C>A LAML-KR 17 1631781 1631781 single base substitution C A synonymous_variant T125T 375C>A LAML-KR 17 1631781 1631781 single base substitution C A synonymous_variant T92T 276C>A LAML-KR 17 1631781 1631781 single base substitution C A upstream_gene_variant LAML-KR 17 1636934 1636934 single base substitution A G downstream_gene_variant LAML-KR 17 1636934 1636934 single base substitution A G exon_variant LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M120V 358A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M1535V 4603A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M166V 496A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M170V 508A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M174V 520A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M308V 922A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M332V 994A>G LAML-KR 17 1636934 1636934 single base substitution A G missense_variant M484V 1450A>G LAML-KR 17 1639071 1639071 single base substitution A T downstream_gene_variant LAML-KR 17 1639071 1639071 single base substitution A T exon_variant LAML-KR 17 1639071 1639071 single base substitution A T intron_variant LAML-KR 17 1642541 1642541 single base substitution G A downstream_gene_variant LAML-KR 17 1643393 1643393 single base substitution A C downstream_gene_variant LAML-KR 17 1643764 1643764 single base substitution G C downstream_gene_variant LAML-KR 17 1644024 1644024 single base substitution G A downstream_gene_variant LAML-KR 17 1644068 1644068 single base substitution C A downstream_gene_variant LAML-KR 17 1644203 1644203 single base substitution C A downstream_gene_variant LAML-KR 17 1644227 1644227 single base substitution G A downstream_gene_variant LAML-KR 17 1644332 1644332 single base substitution G A downstream_gene_variant LGG-US 17 1636086 1636086 single base substitution A G 3_prime_UTR_variant LGG-US 17 1636086 1636086 single base substitution A G downstream_gene_variant LGG-US 17 1636086 1636086 single base substitution A G exon_variant LGG-US 17 1636086 1636086 single base substitution A G missense_variant M115V 343A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M119V 355A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M123V 367A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M1484V 4450A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M257V 769A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M281V 841A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M433V 1297A>G LGG-US 17 1636086 1636086 single base substitution A G missense_variant M69V 205A>G LGG-US 17 1637326 1637326 single base substitution C T downstream_gene_variant LGG-US 17 1637326 1637326 single base substitution C T exon_variant LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S1665S 4995C>T LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S296S 888C>T LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S304S 912C>T LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S438S 1314C>T LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S462S 1386C>T LGG-US 17 1637326 1637326 single base substitution C T synonymous_variant S614S 1842C>T LICA-CN 17 1640859 1640859 single base substitution G T downstream_gene_variant LICA-CN 17 1640859 1640859 single base substitution G T exon_variant LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q1902H 5706G>T LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q533H 1599G>T LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q541H 1623G>T LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q675H 2025G>T LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q699H 2097G>T LICA-CN 17 1640859 1640859 single base substitution G T missense_variant Q851H 2553G>T LICA-FR 17 1627078 1627078 single base substitution C A intron_variant LICA-FR 17 1627078 1627078 single base substitution C A upstream_gene_variant LICA-FR 17 1630392 1630392 single base substitution G A intron_variant LICA-FR 17 1630392 1630392 single base substitution G A synonymous_variant E713E 2139G>A LICA-FR 17 1630392 1630392 single base substitution G A upstream_gene_variant LICA-FR 17 1634431 1634431 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LICA-FR 17 1634431 1634431 single base substitution G A downstream_gene_variant LICA-FR 17 1634431 1634431 single base substitution G A exon_variant LICA-FR 17 1634431 1634431 single base substitution G A intron_variant LICA-FR 17 1634431 1634431 single base substitution G A missense_variant V119M 355G>A LICA-FR 17 1634431 1634431 single base substitution G A missense_variant V1346M 4036G>A LICA-FR 17 1634431 1634431 single base substitution G A missense_variant V143M 427G>A LICA-FR 17 1634431 1634431 single base substitution G A missense_variant V295M 883G>A LICA-FR 17 1634431 1634431 single base substitution G A upstream_gene_variant LICA-FR 17 1638072 1638072 deletion of <=200bp C - downstream_gene_variant LICA-FR 17 1638072 1638072 deletion of <=200bp C - intron_variant LICA-FR 17 1638940 1638940 single base substitution C A downstream_gene_variant LICA-FR 17 1638940 1638940 single base substitution C A exon_variant LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H1752N 5254C>A LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H383N 1147C>A LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H391N 1171C>A LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H525N 1573C>A LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H549N 1645C>A LICA-FR 17 1638940 1638940 single base substitution C A missense_variant H701N 2101C>A LICA-FR 17 1642600 1642600 single base substitution G C downstream_gene_variant LICA-FR 17 1642658 1642658 single base substitution T C downstream_gene_variant LICA-FR 17 1642678 1642678 single base substitution C A downstream_gene_variant LICA-FR 17 1644113 1644113 single base substitution C A downstream_gene_variant LIHC-US 17 1630783 1630783 single base substitution C T intron_variant LIHC-US 17 1630783 1630783 single base substitution C T stop_gained Q844* 2530C>T LIHC-US 17 1630783 1630783 single base substitution C T upstream_gene_variant LIHC-US 17 1634133 1634133 single base substitution T C 5_prime_UTR_variant LIHC-US 17 1634133 1634133 single base substitution T C downstream_gene_variant LIHC-US 17 1634133 1634133 single base substitution T C exon_variant LIHC-US 17 1634133 1634133 single base substitution T C intron_variant LIHC-US 17 1634133 1634133 single base substitution T C missense_variant L1287P 3860T>C LIHC-US 17 1634133 1634133 single base substitution T C missense_variant L167P 500T>C LIHC-US 17 1634133 1634133 single base substitution T C missense_variant L236P 707T>C LIHC-US 17 1634133 1634133 single base substitution T C missense_variant L60P 179T>C LIHC-US 17 1634133 1634133 single base substitution T C missense_variant L84P 251T>C LIHC-US 17 1634133 1634133 single base substitution T C upstream_gene_variant LINC-JP 17 1620566 1620566 single base substitution T C intron_variant LINC-JP 17 1628833 1628837 deletion of <=200bp GAAAC - frameshift_variant ET194 LINC-JP 17 1628833 1628837 deletion of <=200bp GAAAC - intron_variant LINC-JP 17 1628833 1628837 deletion of <=200bp GAAAC - upstream_gene_variant LINC-JP 17 1630184 1630184 single base substitution A T intron_variant LINC-JP 17 1630184 1630184 single base substitution A T missense_variant E644V 1931A>T LINC-JP 17 1630184 1630184 single base substitution A T upstream_gene_variant LINC-JP 17 1633872 1633872 single base substitution C G exon_variant LINC-JP 17 1633872 1633872 single base substitution C G intron_variant LINC-JP 17 1633872 1633872 single base substitution C G upstream_gene_variant LINC-JP 17 1635236 1635236 insertion of <=200bp - TA downstream_gene_variant LINC-JP 17 1635236 1635236 insertion of <=200bp - TA intron_variant LIRI-JP 17 1615371 1615371 single base substitution A G upstream_gene_variant LIRI-JP 17 1617478 1617478 single base substitution G A upstream_gene_variant LIRI-JP 17 1622483 1622483 single base substitution A G intron_variant LIRI-JP 17 1623683 1623683 single base substitution A T intron_variant LIRI-JP 17 1623683 1623683 single base substitution A T upstream_gene_variant LIRI-JP 17 1624497 1624497 single base substitution A G intron_variant LIRI-JP 17 1624497 1624497 single base substitution A G upstream_gene_variant LIRI-JP 17 1636393 1636393 single base substitution G T downstream_gene_variant LIRI-JP 17 1636393 1636393 single base substitution G T intron_variant LIRI-JP 17 1639911 1639911 single base substitution C G downstream_gene_variant LIRI-JP 17 1639911 1639911 single base substitution C G intron_variant LUSC-KR 17 1616040 1616040 single base substitution G T upstream_gene_variant LUSC-KR 17 1616498 1616498 single base substitution G A upstream_gene_variant LUSC-KR 17 1616512 1616512 single base substitution C G upstream_gene_variant LUSC-KR 17 1619679 1619679 single base substitution T G upstream_gene_variant LUSC-KR 17 1624501 1624501 single base substitution A C intron_variant LUSC-KR 17 1624501 1624501 single base substitution A C upstream_gene_variant LUSC-KR 17 1635152 1635152 single base substitution C A downstream_gene_variant LUSC-KR 17 1635152 1635152 single base substitution C A intron_variant LUSC-KR 17 1638689 1638689 single base substitution C T downstream_gene_variant LUSC-KR 17 1638689 1638689 single base substitution C T intron_variant LUSC-KR 17 1642654 1642654 single base substitution A G downstream_gene_variant LUSC-KR 17 1643168 1643168 single base substitution A C downstream_gene_variant LUSC-KR 17 1643462 1643462 single base substitution A G downstream_gene_variant LUSC-KR 17 1643709 1643709 single base substitution G A downstream_gene_variant LUSC-KR 17 1643764 1643764 single base substitution G C downstream_gene_variant LUSC-KR 17 1643934 1643934 single base substitution G A downstream_gene_variant LUSC-KR 17 1644023 1644023 single base substitution C A downstream_gene_variant LUSC-KR 17 1644227 1644227 single base substitution G A downstream_gene_variant LUSC-KR 17 1644269 1644269 single base substitution A G downstream_gene_variant LUSC-KR 17 1644269 1644269 single base substitution A T downstream_gene_variant LUSC-KR 17 1644284 1644284 single base substitution G A downstream_gene_variant LUSC-KR 17 1644285 1644285 single base substitution G A downstream_gene_variant LUSC-KR 17 1644555 1644555 single base substitution G A downstream_gene_variant LUSC-US 17 1638985 1638985 single base substitution G A downstream_gene_variant LUSC-US 17 1638985 1638985 single base substitution G A exon_variant LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V1767M 5299G>A LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V398M 1192G>A LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V406M 1216G>A LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V540M 1618G>A LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V564M 1690G>A LUSC-US 17 1638985 1638985 single base substitution G A missense_variant V716M 2146G>A MALY-DE 17 1625982 1625982 single base substitution T C intron_variant MALY-DE 17 1625982 1625982 single base substitution T C upstream_gene_variant MALY-DE 17 1634495 1634495 single base substitution G A downstream_gene_variant MALY-DE 17 1634495 1634495 single base substitution G A exon_variant MALY-DE 17 1634495 1634495 single base substitution G A intron_variant MALY-DE 17 1634495 1634495 single base substitution G A missense_variant R1367Q 4100G>A MALY-DE 17 1634495 1634495 single base substitution G A missense_variant R140Q 419G>A MALY-DE 17 1634495 1634495 single base substitution G A missense_variant R164Q 491G>A MALY-DE 17 1634495 1634495 single base substitution G A missense_variant R316Q 947G>A MALY-DE 17 1634495 1634495 single base substitution G A missense_variant R6Q 17G>A MALY-DE 17 1641244 1641244 single base substitution G A 3_prime_UTR_variant MALY-DE 17 1641244 1641244 single base substitution G A downstream_gene_variant MALY-DE 17 1641244 1641244 single base substitution G A exon_variant MELA-AU 17 1616083 1616083 single base substitution G A upstream_gene_variant MELA-AU 17 1616336 1616336 single base substitution G A upstream_gene_variant MELA-AU 17 1616479 1616479 single base substitution G A upstream_gene_variant MELA-AU 17 1616915 1616915 single base substitution A G upstream_gene_variant MELA-AU 17 1616917 1616918 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 1617223 1617223 single base substitution G A upstream_gene_variant MELA-AU 17 1617289 1617289 single base substitution G A upstream_gene_variant MELA-AU 17 1617499 1617499 single base substitution C T upstream_gene_variant MELA-AU 17 1617733 1617733 single base substitution G A upstream_gene_variant MELA-AU 17 1618080 1618080 single base substitution C T upstream_gene_variant MELA-AU 17 1618708 1618709 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 1618771 1618771 insertion of <=200bp - G upstream_gene_variant MELA-AU 17 1619003 1619003 single base substitution G A upstream_gene_variant MELA-AU 17 1619332 1619333 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 1619427 1619427 single base substitution G A upstream_gene_variant MELA-AU 17 1619632 1619632 single base substitution G A upstream_gene_variant MELA-AU 17 1619651 1619651 single base substitution C T upstream_gene_variant MELA-AU 17 1619656 1619656 single base substitution C T upstream_gene_variant MELA-AU 17 1619669 1619669 single base substitution G A upstream_gene_variant MELA-AU 17 1619691 1619691 single base substitution G A upstream_gene_variant MELA-AU 17 1619692 1619692 single base substitution G A upstream_gene_variant MELA-AU 17 1619710 1619710 single base substitution G A upstream_gene_variant MELA-AU 17 1619723 1619723 single base substitution G A upstream_gene_variant MELA-AU 17 1622854 1622854 insertion of <=200bp - AC intron_variant MELA-AU 17 1622854 1622854 insertion of <=200bp - AC upstream_gene_variant MELA-AU 17 1624086 1624086 single base substitution C T intron_variant MELA-AU 17 1624086 1624086 single base substitution C T upstream_gene_variant MELA-AU 17 1624262 1624262 single base substitution G A intron_variant MELA-AU 17 1624262 1624262 single base substitution G A upstream_gene_variant MELA-AU 17 1624908 1624908 single base substitution G A intron_variant MELA-AU 17 1624908 1624908 single base substitution G A upstream_gene_variant MELA-AU 17 1625269 1625269 single base substitution T A intron_variant MELA-AU 17 1625269 1625269 single base substitution T A upstream_gene_variant MELA-AU 17 1627948 1627948 single base substitution G A 5_prime_UTR_variant MELA-AU 17 1627948 1627948 single base substitution G A intron_variant MELA-AU 17 1627948 1627948 single base substitution G A upstream_gene_variant MELA-AU 17 1628975 1628975 single base substitution C T intron_variant MELA-AU 17 1628975 1628975 single base substitution C T missense_variant S241F 722C>T MELA-AU 17 1628975 1628975 single base substitution C T upstream_gene_variant MELA-AU 17 1629515 1629515 single base substitution G A intron_variant MELA-AU 17 1629515 1629515 single base substitution G A missense_variant R421Q 1262G>A MELA-AU 17 1629515 1629515 single base substitution G A upstream_gene_variant MELA-AU 17 1629775 1629775 single base substitution G A intron_variant MELA-AU 17 1629775 1629775 single base substitution G A missense_variant D508N 1522G>A MELA-AU 17 1629775 1629775 single base substitution G A upstream_gene_variant MELA-AU 17 1631347 1631347 single base substitution G A 5_prime_UTR_variant MELA-AU 17 1631347 1631347 single base substitution G A exon_variant MELA-AU 17 1631347 1631347 single base substitution G A intron_variant MELA-AU 17 1631347 1631347 single base substitution G A missense_variant E1032K 3094G>A MELA-AU 17 1631347 1631347 single base substitution G A upstream_gene_variant MELA-AU 17 1631951 1631951 single base substitution A G intron_variant MELA-AU 17 1631951 1631951 single base substitution A G upstream_gene_variant MELA-AU 17 1632130 1632130 single base substitution C T intron_variant MELA-AU 17 1632130 1632130 single base substitution C T upstream_gene_variant MELA-AU 17 1632171 1632171 single base substitution C T intron_variant MELA-AU 17 1632171 1632171 single base substitution C T upstream_gene_variant MELA-AU 17 1632360 1632360 single base substitution G A intron_variant MELA-AU 17 1632360 1632360 single base substitution G A upstream_gene_variant MELA-AU 17 1633294 1633294 single base substitution A G intron_variant MELA-AU 17 1633294 1633294 single base substitution A G upstream_gene_variant MELA-AU 17 1634545 1634545 single base substitution G A downstream_gene_variant MELA-AU 17 1634545 1634545 single base substitution G A exon_variant MELA-AU 17 1634545 1634545 single base substitution G A intron_variant MELA-AU 17 1634545 1634545 single base substitution G A missense_variant V1384I 4150G>A MELA-AU 17 1634545 1634545 single base substitution G A missense_variant V157I 469G>A MELA-AU 17 1634545 1634545 single base substitution G A missense_variant V181I 541G>A MELA-AU 17 1634545 1634545 single base substitution G A missense_variant V23I 67G>A MELA-AU 17 1634545 1634545 single base substitution G A missense_variant V333I 997G>A MELA-AU 17 1634894 1634894 single base substitution C T downstream_gene_variant MELA-AU 17 1634894 1634894 single base substitution C T intron_variant MELA-AU 17 1635079 1635079 single base substitution C T downstream_gene_variant MELA-AU 17 1635079 1635079 single base substitution C T intron_variant MELA-AU 17 1635296 1635296 single base substitution G A downstream_gene_variant MELA-AU 17 1635296 1635296 single base substitution G A intron_variant MELA-AU 17 1635485 1635485 single base substitution C T downstream_gene_variant MELA-AU 17 1635485 1635485 single base substitution C T intron_variant MELA-AU 17 1636078 1636078 single base substitution C T 3_prime_UTR_variant MELA-AU 17 1636078 1636078 single base substitution C T downstream_gene_variant MELA-AU 17 1636078 1636078 single base substitution C T exon_variant MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T112I 335C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T116I 347C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T120I 359C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T1481I 4442C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T254I 761C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T278I 833C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T430I 1289C>T MELA-AU 17 1636078 1636078 single base substitution C T missense_variant T66I 197C>T MELA-AU 17 1636271 1636271 single base substitution C T downstream_gene_variant MELA-AU 17 1636271 1636271 single base substitution C T exon_variant MELA-AU 17 1636271 1636271 single base substitution C T intron_variant MELA-AU 17 1636488 1636488 single base substitution C T downstream_gene_variant MELA-AU 17 1636488 1636488 single base substitution C T intron_variant MELA-AU 17 1636789 1636789 single base substitution C T downstream_gene_variant MELA-AU 17 1636789 1636789 single base substitution C T intron_variant MELA-AU 17 1636802 1636802 single base substitution C T downstream_gene_variant MELA-AU 17 1636802 1636802 single base substitution C T intron_variant MELA-AU 17 1637320 1637320 single base substitution C T downstream_gene_variant MELA-AU 17 1637320 1637320 single base substitution C T exon_variant MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F1663F 4989C>T MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F294F 882C>T MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F302F 906C>T MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F436F 1308C>T MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F460F 1380C>T MELA-AU 17 1637320 1637320 single base substitution C T synonymous_variant F612F 1836C>T MELA-AU 17 1637605 1637605 single base substitution G A downstream_gene_variant MELA-AU 17 1637605 1637605 single base substitution G A intron_variant MELA-AU 17 1639534 1639534 single base substitution C T downstream_gene_variant MELA-AU 17 1639534 1639534 single base substitution C T intron_variant MELA-AU 17 1640179 1640180 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 1640179 1640180 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 1640561 1640561 single base substitution C T downstream_gene_variant MELA-AU 17 1640561 1640561 single base substitution C T intron_variant MELA-AU 17 1641667 1641667 single base substitution C T 3_prime_UTR_variant MELA-AU 17 1641667 1641667 single base substitution C T downstream_gene_variant MELA-AU 17 1641667 1641667 single base substitution C T exon_variant MELA-AU 17 1641811 1641811 single base substitution T C 3_prime_UTR_variant MELA-AU 17 1641811 1641811 single base substitution T C downstream_gene_variant MELA-AU 17 1641811 1641811 single base substitution T C exon_variant MELA-AU 17 1641866 1641866 single base substitution C T 3_prime_UTR_variant MELA-AU 17 1641866 1641866 single base substitution C T downstream_gene_variant MELA-AU 17 1641866 1641866 single base substitution C T exon_variant MELA-AU 17 1642629 1642629 single base substitution G A downstream_gene_variant MELA-AU 17 1644893 1644893 single base substitution G A downstream_gene_variant MELA-AU 17 1645592 1645592 single base substitution G A downstream_gene_variant MELA-AU 17 1645918 1645918 single base substitution C T downstream_gene_variant MELA-AU 17 1646100 1646100 single base substitution G A downstream_gene_variant MELA-AU 17 1646133 1646134 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant ORCA-IN 17 1631193 1631193 single base substitution C T exon_variant ORCA-IN 17 1631193 1631193 single base substitution C T intron_variant ORCA-IN 17 1631193 1631193 single base substitution C T synonymous_variant F980F 2940C>T ORCA-IN 17 1631193 1631193 single base substitution C T upstream_gene_variant ORCA-IN 17 1636121 1636121 single base substitution G T 3_prime_UTR_variant ORCA-IN 17 1636121 1636121 single base substitution G T downstream_gene_variant ORCA-IN 17 1636121 1636121 single base substitution G T exon_variant ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L126L 378G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L130L 390G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L134L 402G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L1495L 4485G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L268L 804G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L292L 876G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L444L 1332G>T ORCA-IN 17 1636121 1636121 single base substitution G T synonymous_variant L80L 240G>T ORCA-IN 17 1637371 1637371 single base substitution C T downstream_gene_variant ORCA-IN 17 1637371 1637371 single base substitution C T exon_variant ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y1680Y 5040C>T ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y311Y 933C>T ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y319Y 957C>T ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y453Y 1359C>T ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y477Y 1431C>T ORCA-IN 17 1637371 1637371 single base substitution C T synonymous_variant Y629Y 1887C>T ORCA-IN 17 1638979 1638979 single base substitution C T downstream_gene_variant ORCA-IN 17 1638979 1638979 single base substitution C T exon_variant ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R1765C 5293C>T ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R396C 1186C>T ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R404C 1210C>T ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R538C 1612C>T ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R562C 1684C>T ORCA-IN 17 1638979 1638979 single base substitution C T missense_variant R714C 2140C>T OV-AU 17 1616219 1616219 single base substitution G C upstream_gene_variant OV-AU 17 1619931 1619931 single base substitution A C 5_prime_UTR_variant OV-AU 17 1619931 1619931 single base substitution A C intron_variant OV-AU 17 1627099 1627099 single base substitution C T intron_variant OV-AU 17 1627099 1627099 single base substitution C T upstream_gene_variant OV-AU 17 1641154 1641154 single base substitution A G 3_prime_UTR_variant OV-AU 17 1641154 1641154 single base substitution A G downstream_gene_variant OV-AU 17 1641154 1641154 single base substitution A G exon_variant PACA-AU 17 1629646 1629646 single base substitution G A intron_variant PACA-AU 17 1629646 1629646 single base substitution G A missense_variant G465R 1393G>A PACA-AU 17 1629646 1629646 single base substitution G A upstream_gene_variant PACA-AU 17 1631341 1631343 deletion of <=200bp GAG - 5_prime_UTR_variant PACA-AU 17 1631341 1631343 deletion of <=200bp GAG - exon_variant PACA-AU 17 1631341 1631343 deletion of <=200bp GAG - inframe_deletion E1030 PACA-AU 17 1631341 1631343 deletion of <=200bp GAG - intron_variant PACA-AU 17 1631341 1631343 deletion of <=200bp GAG - upstream_gene_variant PACA-CA 17 1628916 1628916 single base substitution T C intron_variant PACA-CA 17 1628916 1628916 single base substitution T C synonymous_variant A221A 663T>C PACA-CA 17 1628916 1628916 single base substitution T C upstream_gene_variant PACA-CA 17 1630615 1630615 single base substitution C T intron_variant PACA-CA 17 1630615 1630615 single base substitution C T missense_variant R788W 2362C>T PACA-CA 17 1630615 1630615 single base substitution C T upstream_gene_variant PACA-CA 17 1633297 1633297 single base substitution A G intron_variant PACA-CA 17 1633297 1633297 single base substitution A G upstream_gene_variant PACA-CA 17 1634638 1634638 single base substitution G A downstream_gene_variant PACA-CA 17 1634638 1634638 single base substitution G A intron_variant PACA-CA 17 1635888 1635888 single base substitution C T downstream_gene_variant PACA-CA 17 1635888 1635888 single base substitution C T intron_variant PACA-CA 17 1636141 1636141 single base substitution G A downstream_gene_variant PACA-CA 17 1636141 1636141 single base substitution G A exon_variant PACA-CA 17 1636141 1636141 single base substitution G A intron_variant PACA-CA 17 1637922 1637922 single base substitution A C downstream_gene_variant PACA-CA 17 1637922 1637922 single base substitution A C intron_variant PACA-CA 17 1646315 1646315 single base substitution C T downstream_gene_variant PACA-CA 17 1646775 1646775 single base substitution T C downstream_gene_variant PAEN-AU 17 1618076 1618076 single base substitution A G upstream_gene_variant PAEN-IT 17 1634995 1634995 single base substitution A T downstream_gene_variant PAEN-IT 17 1634995 1634995 single base substitution A T intron_variant PBCA-DE 17 1617547 1617547 single base substitution T A upstream_gene_variant PBCA-DE 17 1640897 1640897 single base substitution C T downstream_gene_variant PBCA-DE 17 1640897 1640897 single base substitution C T exon_variant PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T1915M 5744C>T PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T546M 1637C>T PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T554M 1661C>T PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T688M 2063C>T PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T712M 2135C>T PBCA-DE 17 1640897 1640897 single base substitution C T missense_variant T864M 2591C>T PBCA-DE 17 1646404 1646404 single base substitution G A downstream_gene_variant PRAD-CA 17 1641889 1641889 single base substitution C T 3_prime_UTR_variant PRAD-CA 17 1641889 1641889 single base substitution C T downstream_gene_variant PRAD-UK 17 1629501 1629501 single base substitution G A intron_variant PRAD-UK 17 1629501 1629501 single base substitution G A synonymous_variant T416T 1248G>A PRAD-UK 17 1629501 1629501 single base substitution G A upstream_gene_variant PRAD-US 17 1631341 1631343 deletion of <=200bp GAG - 5_prime_UTR_variant PRAD-US 17 1631341 1631343 deletion of <=200bp GAG - exon_variant PRAD-US 17 1631341 1631343 deletion of <=200bp GAG - inframe_deletion E1030 PRAD-US 17 1631341 1631343 deletion of <=200bp GAG - intron_variant PRAD-US 17 1631341 1631343 deletion of <=200bp GAG - upstream_gene_variant PRAD-US 17 1633695 1633695 single base substitution G T exon_variant PRAD-US 17 1633695 1633695 single base substitution G T intron_variant PRAD-US 17 1633695 1633695 single base substitution G T missense_variant R1230L 3689G>T PRAD-US 17 1633695 1633695 single base substitution G T missense_variant R179L 536G>T PRAD-US 17 1633695 1633695 single base substitution G T missense_variant R27L 80G>T PRAD-US 17 1633695 1633695 single base substitution G T missense_variant R3L 8G>T PRAD-US 17 1633695 1633695 single base substitution G T upstream_gene_variant PRAD-US 17 1637102 1637102 deletion of <=200bp G - downstream_gene_variant PRAD-US 17 1637102 1637102 deletion of <=200bp G - exon_variant PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G1591 PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G222 PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G230 PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G364 PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G388 PRAD-US 17 1637102 1637102 deletion of <=200bp G - frameshift_variant G540 READ-US 17 1629889 1629889 single base substitution G A intron_variant READ-US 17 1629889 1629889 single base substitution G A missense_variant D546N 1636G>A READ-US 17 1629889 1629889 single base substitution G A upstream_gene_variant RECA-EU 17 1634655 1634655 single base substitution G T downstream_gene_variant RECA-EU 17 1634655 1634655 single base substitution G T intron_variant SKCA-BR 17 1616737 1616737 single base substitution G A upstream_gene_variant SKCA-BR 17 1618970 1618970 single base substitution G A upstream_gene_variant SKCA-BR 17 1619248 1619248 single base substitution G A upstream_gene_variant SKCA-BR 17 1620408 1620408 single base substitution C T intron_variant SKCA-BR 17 1620409 1620409 single base substitution C T intron_variant SKCA-BR 17 1623335 1623335 single base substitution G A intron_variant SKCA-BR 17 1623335 1623335 single base substitution G A upstream_gene_variant SKCA-BR 17 1625641 1625642 deletion of <=200bp CT - intron_variant SKCA-BR 17 1625641 1625642 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 17 1626745 1626751 deletion of <=200bp ATTTATT - intron_variant SKCA-BR 17 1626745 1626751 deletion of <=200bp ATTTATT - upstream_gene_variant SKCA-BR 17 1626753 1626753 single base substitution T A intron_variant SKCA-BR 17 1626753 1626753 single base substitution T A upstream_gene_variant SKCA-BR 17 1626755 1626755 single base substitution A T intron_variant SKCA-BR 17 1626755 1626755 single base substitution A T upstream_gene_variant SKCA-BR 17 1626761 1626763 deletion of <=200bp TTA - intron_variant SKCA-BR 17 1626761 1626763 deletion of <=200bp TTA - upstream_gene_variant SKCA-BR 17 1627023 1627023 single base substitution G C intron_variant SKCA-BR 17 1627023 1627023 single base substitution G C upstream_gene_variant SKCA-BR 17 1627382 1627382 single base substitution G A intron_variant SKCA-BR 17 1627382 1627382 single base substitution G A upstream_gene_variant SKCA-BR 17 1628161 1628161 single base substitution T C intron_variant SKCA-BR 17 1628161 1628161 single base substitution T C upstream_gene_variant SKCA-BR 17 1631853 1631853 single base substitution A G exon_variant SKCA-BR 17 1631853 1631853 single base substitution A G intron_variant SKCA-BR 17 1631853 1631853 single base substitution A G synonymous_variant G116G 348A>G SKCA-BR 17 1631853 1631853 single base substitution A G synonymous_variant G1200G 3600A>G SKCA-BR 17 1631853 1631853 single base substitution A G synonymous_variant G149G 447A>G SKCA-BR 17 1631853 1631853 single base substitution A G upstream_gene_variant SKCA-BR 17 1633377 1633377 single base substitution A G intron_variant SKCA-BR 17 1633377 1633377 single base substitution A G upstream_gene_variant SKCA-BR 17 1638072 1638072 single base substitution C A downstream_gene_variant SKCA-BR 17 1638072 1638072 single base substitution C A intron_variant SKCA-BR 17 1638072 1638073 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 17 1638072 1638073 deletion of <=200bp CA - intron_variant SKCA-BR 17 1642181 1642181 single base substitution G A downstream_gene_variant SKCA-BR 17 1643663 1643663 single base substitution C A downstream_gene_variant SKCA-BR 17 1644092 1644092 single base substitution A G downstream_gene_variant SKCA-BR 17 1645371 1645371 single base substitution A T downstream_gene_variant SKCA-BR 17 1645373 1645373 single base substitution C T downstream_gene_variant SKCA-BR 17 1645410 1645410 single base substitution C T downstream_gene_variant SKCA-BR 17 1645452 1645452 single base substitution C T downstream_gene_variant SKCM-US 17 1631341 1631343 deletion of <=200bp GAG - 5_prime_UTR_variant SKCM-US 17 1631341 1631343 deletion of <=200bp GAG - exon_variant SKCM-US 17 1631341 1631343 deletion of <=200bp GAG - inframe_deletion E1030 SKCM-US 17 1631341 1631343 deletion of <=200bp GAG - intron_variant SKCM-US 17 1631341 1631343 deletion of <=200bp GAG - upstream_gene_variant SKCM-US 17 1631537 1631537 single base substitution C T exon_variant SKCM-US 17 1631537 1631537 single base substitution C T intron_variant SKCM-US 17 1631537 1631537 single base substitution C T missense_variant P1095L 3284C>T SKCM-US 17 1631537 1631537 single base substitution C T missense_variant P11L 32C>T SKCM-US 17 1631537 1631537 single base substitution C T missense_variant P44L 131C>T SKCM-US 17 1631537 1631537 single base substitution C T upstream_gene_variant SKCM-US 17 1631593 1631593 single base substitution A G exon_variant SKCM-US 17 1631593 1631593 single base substitution A G intron_variant SKCM-US 17 1631593 1631593 single base substitution A G missense_variant T1114A 3340A>G SKCM-US 17 1631593 1631593 single base substitution A G missense_variant T30A 88A>G SKCM-US 17 1631593 1631593 single base substitution A G missense_variant T63A 187A>G SKCM-US 17 1631593 1631593 single base substitution A G upstream_gene_variant SKCM-US 17 1631646 1631646 single base substitution C T exon_variant SKCM-US 17 1631646 1631646 single base substitution C T intron_variant SKCM-US 17 1631646 1631646 single base substitution C T synonymous_variant P1131P 3393C>T SKCM-US 17 1631646 1631646 single base substitution C T synonymous_variant P47P 141C>T SKCM-US 17 1631646 1631646 single base substitution C T synonymous_variant P80P 240C>T SKCM-US 17 1631646 1631646 single base substitution C T upstream_gene_variant SKCM-US 17 1631701 1631701 single base substitution G C exon_variant SKCM-US 17 1631701 1631701 single base substitution G C intron_variant SKCM-US 17 1631701 1631701 single base substitution G C missense_variant E1150Q 3448G>C SKCM-US 17 1631701 1631701 single base substitution G C missense_variant E66Q 196G>C SKCM-US 17 1631701 1631701 single base substitution G C missense_variant E99Q 295G>C SKCM-US 17 1631701 1631701 single base substitution G C upstream_gene_variant SKCM-US 17 1634460 1634460 single base substitution C T 5_prime_UTR_variant SKCM-US 17 1634460 1634460 single base substitution C T downstream_gene_variant SKCM-US 17 1634460 1634460 single base substitution C T exon_variant SKCM-US 17 1634460 1634460 single base substitution C T intron_variant SKCM-US 17 1634460 1634460 single base substitution C T synonymous_variant Y128Y 384C>T SKCM-US 17 1634460 1634460 single base substitution C T synonymous_variant Y1355Y 4065C>T SKCM-US 17 1634460 1634460 single base substitution C T synonymous_variant Y152Y 456C>T SKCM-US 17 1634460 1634460 single base substitution C T synonymous_variant Y304Y 912C>T SKCM-US 17 1634460 1634460 single base substitution C T upstream_gene_variant SKCM-US 17 1636905 1636905 single base substitution G A downstream_gene_variant SKCM-US 17 1636905 1636905 single base substitution G A exon_variant SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S110N 329G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S1525N 4574G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S156N 467G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S160N 479G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S164N 491G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S298N 893G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S322N 965G>A SKCM-US 17 1636905 1636905 single base substitution G A missense_variant S474N 1421G>A SKCM-US 17 1637215 1637215 single base substitution C T downstream_gene_variant SKCM-US 17 1637215 1637215 single base substitution C T exon_variant SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S1628S 4884C>T SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S259S 777C>T SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S267S 801C>T SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S401S 1203C>T SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S425S 1275C>T SKCM-US 17 1637215 1637215 single base substitution C T synonymous_variant S577S 1731C>T SKCM-US 17 1637235 1637235 single base substitution A T downstream_gene_variant SKCM-US 17 1637235 1637235 single base substitution A T exon_variant SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H1635L 4904A>T SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H266L 797A>T SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H274L 821A>T SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H408L 1223A>T SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H432L 1295A>T SKCM-US 17 1637235 1637235 single base substitution A T missense_variant H584L 1751A>T SKCM-US 17 1637434 1637434 single base substitution C T downstream_gene_variant SKCM-US 17 1637434 1637434 single base substitution C T exon_variant SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F1701F 5103C>T SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F332F 996C>T SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F340F 1020C>T SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F474F 1422C>T SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F498F 1494C>T SKCM-US 17 1637434 1637434 single base substitution C T synonymous_variant F650F 1950C>T STAD-US 17 1631634 1631634 deletion of <=200bp G - exon_variant STAD-US 17 1631634 1631634 deletion of <=200bp G - frameshift_variant E1127 STAD-US 17 1631634 1631634 deletion of <=200bp G - frameshift_variant E43 STAD-US 17 1631634 1631634 deletion of <=200bp G - frameshift_variant E76 STAD-US 17 1631634 1631634 deletion of <=200bp G - intron_variant STAD-US 17 1631634 1631634 deletion of <=200bp G - upstream_gene_variant STAD-US 17 1634162 1634162 single base substitution A G 5_prime_UTR_variant STAD-US 17 1634162 1634162 single base substitution A G downstream_gene_variant STAD-US 17 1634162 1634162 single base substitution A G exon_variant STAD-US 17 1634162 1634162 single base substitution A G intron_variant STAD-US 17 1634162 1634162 single base substitution A G missense_variant S1297G 3889A>G STAD-US 17 1634162 1634162 single base substitution A G missense_variant S177G 529A>G STAD-US 17 1634162 1634162 single base substitution A G missense_variant S246G 736A>G STAD-US 17 1634162 1634162 single base substitution A G missense_variant S70G 208A>G STAD-US 17 1634162 1634162 single base substitution A G missense_variant S94G 280A>G STAD-US 17 1634162 1634162 single base substitution A G upstream_gene_variant STAD-US 17 1634494 1634494 single base substitution C T downstream_gene_variant STAD-US 17 1634494 1634494 single base substitution C T exon_variant STAD-US 17 1634494 1634494 single base substitution C T intron_variant STAD-US 17 1634494 1634494 single base substitution C T missense_variant R1367W 4099C>T STAD-US 17 1634494 1634494 single base substitution C T missense_variant R140W 418C>T STAD-US 17 1634494 1634494 single base substitution C T missense_variant R164W 490C>T STAD-US 17 1634494 1634494 single base substitution C T missense_variant R316W 946C>T STAD-US 17 1634494 1634494 single base substitution C T missense_variant R6W 16C>T STAD-US 17 1635975 1635975 single base substitution C T 3_prime_UTR_variant STAD-US 17 1635975 1635975 single base substitution C T downstream_gene_variant STAD-US 17 1635975 1635975 single base substitution C T exon_variant STAD-US 17 1635975 1635975 single base substitution C T missense_variant P1447S 4339C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P220S 658C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P244S 730C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P32S 94C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P396S 1186C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P78S 232C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P82S 244C>T STAD-US 17 1635975 1635975 single base substitution C T missense_variant P86S 256C>T STAD-US 17 1636038 1636038 single base substitution G A 3_prime_UTR_variant STAD-US 17 1636038 1636038 single base substitution G A downstream_gene_variant STAD-US 17 1636038 1636038 single base substitution G A exon_variant STAD-US 17 1636038 1636038 single base substitution G A missense_variant V103M 307G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V107M 319G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V1468M 4402G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V241M 721G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V265M 793G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V417M 1249G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V53M 157G>A STAD-US 17 1636038 1636038 single base substitution G A missense_variant V99M 295G>A STAD-US 17 1636825 1636825 single base substitution C T 3_prime_UTR_variant STAD-US 17 1636825 1636825 single base substitution C T downstream_gene_variant STAD-US 17 1636825 1636825 single base substitution C T exon_variant STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D129D 387C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D133D 399C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D137D 411C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D1498D 4494C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D271D 813C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D295D 885C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D447D 1341C>T STAD-US 17 1636825 1636825 single base substitution C T synonymous_variant D83D 249C>T STAD-US 17 1637274 1637274 single base substitution C T downstream_gene_variant STAD-US 17 1637274 1637274 single base substitution C T exon_variant STAD-US 17 1637274 1637274 single base substitution C T missense_variant S1648L 4943C>T STAD-US 17 1637274 1637274 single base substitution C T missense_variant S279L 836C>T STAD-US 17 1637274 1637274 single base substitution C T missense_variant S287L 860C>T STAD-US 17 1637274 1637274 single base substitution C T missense_variant S421L 1262C>T STAD-US 17 1637274 1637274 single base substitution C T missense_variant S445L 1334C>T STAD-US 17 1637274 1637274 single base substitution C T missense_variant S597L 1790C>T STAD-US 17 1637358 1637358 single base substitution C T downstream_gene_variant STAD-US 17 1637358 1637358 single base substitution C T exon_variant STAD-US 17 1637358 1637358 single base substitution C T missense_variant P1676L 5027C>T STAD-US 17 1637358 1637358 single base substitution C T missense_variant P307L 920C>T STAD-US 17 1637358 1637358 single base substitution C T missense_variant P315L 944C>T STAD-US 17 1637358 1637358 single base substitution C T missense_variant P449L 1346C>T STAD-US 17 1637358 1637358 single base substitution C T missense_variant P473L 1418C>T STAD-US 17 1637358 1637358 single base substitution C T missense_variant P625L 1874C>T STAD-US 17 1637421 1637421 single base substitution G A downstream_gene_variant STAD-US 17 1637421 1637421 single base substitution G A exon_variant STAD-US 17 1637421 1637421 single base substitution G A missense_variant R1697H 5090G>A STAD-US 17 1637421 1637421 single base substitution G A missense_variant R328H 983G>A STAD-US 17 1637421 1637421 single base substitution G A missense_variant R336H 1007G>A STAD-US 17 1637421 1637421 single base substitution G A missense_variant R470H 1409G>A STAD-US 17 1637421 1637421 single base substitution G A missense_variant R494H 1481G>A STAD-US 17 1637421 1637421 single base substitution G A missense_variant R646H 1937G>A STAD-US 17 1638935 1638935 deletion of <=200bp C - downstream_gene_variant STAD-US 17 1638935 1638935 deletion of <=200bp C - exon_variant STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A1750 STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A381 STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A389 STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A523 STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A547 STAD-US 17 1638935 1638935 deletion of <=200bp C - frameshift_variant A699 STAD-US 17 1640830 1640830 single base substitution G A downstream_gene_variant STAD-US 17 1640830 1640830 single base substitution G A exon_variant STAD-US 17 1640830 1640830 single base substitution G A missense_variant V1893I 5677G>A STAD-US 17 1640830 1640830 single base substitution G A missense_variant V524I 1570G>A STAD-US 17 1640830 1640830 single base substitution G A missense_variant V532I 1594G>A STAD-US 17 1640830 1640830 single base substitution G A missense_variant V666I 1996G>A STAD-US 17 1640830 1640830 single base substitution G A missense_variant V690I 2068G>A STAD-US 17 1640830 1640830 single base substitution G A missense_variant V842I 2524G>A THCA-SA 17 1616093 1616093 single base substitution G A upstream_gene_variant THCA-SA 17 1630992 1630992 single base substitution G A exon_variant THCA-SA 17 1630992 1630992 single base substitution G A intron_variant THCA-SA 17 1630992 1630992 single base substitution G A synonymous_variant L913L 2739G>A THCA-SA 17 1630992 1630992 single base substitution G A upstream_gene_variant THCA-SA 17 1634104 1634104 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 17 1634104 1634104 single base substitution C T exon_variant THCA-SA 17 1634104 1634104 single base substitution C T intron_variant THCA-SA 17 1634104 1634104 single base substitution C T synonymous_variant A1277A 3831C>T THCA-SA 17 1634104 1634104 single base substitution C T synonymous_variant A157A 471C>T THCA-SA 17 1634104 1634104 single base substitution C T synonymous_variant A226A 678C>T THCA-SA 17 1634104 1634104 single base substitution C T synonymous_variant A50A 150C>T THCA-SA 17 1634104 1634104 single base substitution C T synonymous_variant A74A 222C>T THCA-SA 17 1634104 1634104 single base substitution C T upstream_gene_variant THCA-SA 17 1637458 1637458 single base substitution G A downstream_gene_variant THCA-SA 17 1637458 1637458 single base substitution G A exon_variant THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P1709P 5127G>A THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P340P 1020G>A THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P348P 1044G>A THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P482P 1446G>A THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P506P 1518G>A THCA-SA 17 1637458 1637458 single base substitution G A synonymous_variant P658P 1974G>A THCA-SA 17 1640793 1640793 single base substitution C T downstream_gene_variant THCA-SA 17 1640793 1640793 single base substitution C T exon_variant THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S1880S 5640C>T THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S511S 1533C>T THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S519S 1557C>T THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S653S 1959C>T THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S677S 2031C>T THCA-SA 17 1640793 1640793 single base substitution C T synonymous_variant S829S 2487C>T THCA-SA 17 1641035 1641035 single base substitution A G 3_prime_UTR_variant THCA-SA 17 1641035 1641035 single base substitution A G downstream_gene_variant THCA-SA 17 1641035 1641035 single base substitution A G exon_variant THCA-SA 17 1641715 1641715 single base substitution G T 3_prime_UTR_variant THCA-SA 17 1641715 1641715 single base substitution G T downstream_gene_variant THCA-SA 17 1641715 1641715 single base substitution G T exon_variant THCA-SA 17 1641806 1641806 single base substitution G A 3_prime_UTR_variant THCA-SA 17 1641806 1641806 single base substitution G A downstream_gene_variant THCA-SA 17 1641806 1641806 single base substitution G A exon_variant UCEC-US 17 1628985 1628985 single base substitution C T intron_variant UCEC-US 17 1628985 1628985 single base substitution C T synonymous_variant D244D 732C>T UCEC-US 17 1628985 1628985 single base substitution C T upstream_gene_variant UCEC-US 17 1629043 1629043 single base substitution C A intron_variant UCEC-US 17 1629043 1629043 single base substitution C A missense_variant L264I 790C>A UCEC-US 17 1629043 1629043 single base substitution C A upstream_gene_variant UCEC-US 17 1629622 1629622 single base substitution C T intron_variant UCEC-US 17 1629622 1629622 single base substitution C T missense_variant R457C 1369C>T UCEC-US 17 1629622 1629622 single base substitution C T upstream_gene_variant UCEC-US 17 1629646 1629646 single base substitution G A intron_variant UCEC-US 17 1629646 1629646 single base substitution G A missense_variant G465R 1393G>A UCEC-US 17 1629646 1629646 single base substitution G A upstream_gene_variant UCEC-US 17 1630463 1630463 single base substitution C T intron_variant UCEC-US 17 1630463 1630463 single base substitution C T missense_variant T737M 2210C>T UCEC-US 17 1630463 1630463 single base substitution C T upstream_gene_variant UCEC-US 17 1630687 1630687 single base substitution A G intron_variant UCEC-US 17 1630687 1630687 single base substitution A G missense_variant K812E 2434A>G UCEC-US 17 1630687 1630687 single base substitution A G upstream_gene_variant UCEC-US 17 1630734 1630734 single base substitution G A intron_variant UCEC-US 17 1630734 1630734 single base substitution G A synonymous_variant Q827Q 2481G>A UCEC-US 17 1630734 1630734 single base substitution G A upstream_gene_variant UCEC-US 17 1630816 1630816 single base substitution C A intron_variant UCEC-US 17 1630816 1630816 single base substitution C A missense_variant L855M 2563C>A UCEC-US 17 1630816 1630816 single base substitution C A upstream_gene_variant UCEC-US 17 1630974 1630974 single base substitution G A exon_variant UCEC-US 17 1630974 1630974 single base substitution G A intron_variant UCEC-US 17 1630974 1630974 single base substitution G A synonymous_variant Q907Q 2721G>A UCEC-US 17 1630974 1630974 single base substitution G A upstream_gene_variant UCEC-US 17 1631034 1631034 single base substitution C T exon_variant UCEC-US 17 1631034 1631034 single base substitution C T intron_variant UCEC-US 17 1631034 1631034 single base substitution C T synonymous_variant F927F 2781C>T UCEC-US 17 1631034 1631034 single base substitution C T upstream_gene_variant UCEC-US 17 1631227 1631227 single base substitution A G exon_variant UCEC-US 17 1631227 1631227 single base substitution A G intron_variant UCEC-US 17 1631227 1631227 single base substitution A G missense_variant M992V 2974A>G UCEC-US 17 1631227 1631227 single base substitution A G upstream_gene_variant UCEC-US 17 1631710 1631710 single base substitution G A exon_variant UCEC-US 17 1631710 1631710 single base substitution G A intron_variant UCEC-US 17 1631710 1631710 single base substitution G A missense_variant E102K 304G>A UCEC-US 17 1631710 1631710 single base substitution G A missense_variant E1153K 3457G>A UCEC-US 17 1631710 1631710 single base substitution G A missense_variant E69K 205G>A UCEC-US 17 1631710 1631710 single base substitution G A upstream_gene_variant UCEC-US 17 1631842 1631842 single base substitution G A exon_variant UCEC-US 17 1631842 1631842 single base substitution G A intron_variant UCEC-US 17 1631842 1631842 single base substitution G A missense_variant G113S 337G>A UCEC-US 17 1631842 1631842 single base substitution G A missense_variant G1197S 3589G>A UCEC-US 17 1631842 1631842 single base substitution G A missense_variant G146S 436G>A UCEC-US 17 1631842 1631842 single base substitution G A upstream_gene_variant UCEC-US 17 1634429 1634429 single base substitution C T 5_prime_UTR_variant UCEC-US 17 1634429 1634429 single base substitution C T downstream_gene_variant UCEC-US 17 1634429 1634429 single base substitution C T exon_variant UCEC-US 17 1634429 1634429 single base substitution C T intron_variant UCEC-US 17 1634429 1634429 single base substitution C T missense_variant A118V 353C>T UCEC-US 17 1634429 1634429 single base substitution C T missense_variant A1345V 4034C>T UCEC-US 17 1634429 1634429 single base substitution C T missense_variant A142V 425C>T UCEC-US 17 1634429 1634429 single base substitution C T missense_variant A294V 881C>T UCEC-US 17 1634429 1634429 single base substitution C T upstream_gene_variant UCEC-US 17 1634545 1634545 single base substitution G A downstream_gene_variant UCEC-US 17 1634545 1634545 single base substitution G A exon_variant UCEC-US 17 1634545 1634545 single base substitution G A intron_variant UCEC-US 17 1634545 1634545 single base substitution G A missense_variant V1384I 4150G>A UCEC-US 17 1634545 1634545 single base substitution G A missense_variant V157I 469G>A UCEC-US 17 1634545 1634545 single base substitution G A missense_variant V181I 541G>A UCEC-US 17 1634545 1634545 single base substitution G A missense_variant V23I 67G>A UCEC-US 17 1634545 1634545 single base substitution G A missense_variant V333I 997G>A UCEC-US 17 1637429 1637429 single base substitution G A downstream_gene_variant UCEC-US 17 1637429 1637429 single base substitution G A exon_variant UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V1700I 5098G>A UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V331I 991G>A UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V339I 1015G>A UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V473I 1417G>A UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V497I 1489G>A UCEC-US 17 1637429 1637429 single base substitution G A missense_variant V649I 1945G>A UCEC-US 17 1637437 1637437 single base substitution C T downstream_gene_variant UCEC-US 17 1637437 1637437 single base substitution C T exon_variant UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F1702F 5106C>T UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F333F 999C>T UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F341F 1023C>T UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F475F 1425C>T UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F499F 1497C>T UCEC-US 17 1637437 1637437 single base substitution C T synonymous_variant F651F 1953C>T UCEC-US 17 1638917 1638917 single base substitution C T downstream_gene_variant UCEC-US 17 1638917 1638917 single base substitution C T exon_variant UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A1744V 5231C>T UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A375V 1124C>T UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A383V 1148C>T UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A517V 1550C>T UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A541V 1622C>T UCEC-US 17 1638917 1638917 single base substitution C T missense_variant A693V 2078C>T UCEC-US 17 1639511 1639511 single base substitution A G downstream_gene_variant UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K1835R 5504A>G UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K466R 1397A>G UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K474R 1421A>G UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K608R 1823A>G UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K632R 1895A>G UCEC-US 17 1639511 1639511 single base substitution A G missense_variant K784R 2351A>G UCEC-US 17 1639511 1639511 single base substitution A G splice_region_variant UCEC-US 17 1640708 1640708 single base substitution C T downstream_gene_variant UCEC-US 17 1640708 1640708 single base substitution C T exon_variant UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T1852I 5555C>T UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T483I 1448C>T UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T491I 1472C>T UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T625I 1874C>T UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T649I 1946C>T UCEC-US 17 1640708 1640708 single base substitution C T missense_variant T801I 2402C>T UCEC-US 17 1640812 1640812 single base substitution G A downstream_gene_variant UCEC-US 17 1640812 1640812 single base substitution G A exon_variant UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V1887M 5659G>A UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V518M 1552G>A UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V526M 1576G>A UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V660M 1978G>A UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V684M 2050G>A UCEC-US 17 1640812 1640812 single base substitution G A missense_variant V836M 2506G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand RMS2083 COSM5880893 c.2248G>A p.V750I Substitution - Missense 17:1736114-1736114 + TCGA-A6-6780-01 COSM1381110 c.5335C>T p.R1779* Substitution - Nonsense 17:1736048-1736048 + DLD1 COSM1679362 c.2573C>A p.S858Y Substitution - Missense 17:1737585-1737585 + SCC-25 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + 587342 COSM1232672 c.571C>T p.P191S Substitution - Missense 17:1725530-1725530 + PTC-7C COSM3755292 c.1818A>G p.L606L Substitution - coding silent 17:1734008-1734008 + TCGA-AX-A0J0-01 COSM975899 c.304G>A p.E102K Substitution - Missense 17:1728416-1728416 + PTC-28C COSM1381116 c.5640C>T p.S1880S Substitution - coding silent 17:1737499-1737499 + COLO678 COSM4621514 c.2155A>C p.I719L Substitution - Missense 17:1727114-1727114 + 03-P152 COSM4579474 c.1672A>G p.S558G Substitution - Missense 17:1733862-1733862 + PTC-7C COSM3755291 c.4971A>G p.L1657L Substitution - coding silent 17:1734008-1734008 + CSCC-29-T COSM4566868 c.4996_4997GG>AT p.G1666I Substitution - Missense 17:1734033-1734034 + OSCC-GB_00820111 COSM4887353 c.5040C>T p.Y1680Y Substitution - coding silent 17:1734077-1734077 + CSCC-32-T COSM4528052 c.1508G>A p.R503H Substitution - Missense 17:1726467-1726467 + CHC433T COSM436117 c.2487C>T p.S829S Substitution - coding silent 17:1737499-1737499 + TCGA-IK-7675-01 COSM3969848 c.4995C>T p.S1665S Substitution - coding silent 17:1734032-1734032 + TCGA-AP-A0LM-01 COSM1588685 c.5659G>A p.V1887M Substitution - Missense 17:1737518-1737518 + TCGA-DK-A3WW-01 COSM3795298 c.5404G>A p.V1802M Substitution - Missense 17:1736117-1736117 + T3509 COSM4741076 c.3693G>T p.W1231C Substitution - Missense 17:1730405-1730405 + B106-Tumor COSM3932488 c.1450A>G p.M484V Substitution - Missense 17:1733640-1733640 + TCGA-AP-A0LM-01 COSM975939 c.2506G>A p.V836M Substitution - Missense 17:1737518-1737518 + S00832 COSM5660841 c.2741A>G p.K914R Substitution - Missense 17:1727700-1727700 + YUDIVI COSM5385762 c.4710C>T p.I1570I Substitution - coding silent 17:1733747-1733747 + TCGA-FP-7998-01 COSM4064199 c.4339C>T p.P1447S Substitution - Missense 17:1732681-1732681 + BCB325T COSM4788528 c.5254C>A p.H1752N Substitution - Missense 17:1735646-1735646 + SC_9010 COSM5565510 c.923G>A p.R308K Substitution - Missense 17:1725882-1725882 + PTC-7C COSM436117 c.2487C>T p.S829S Substitution - coding silent 17:1737499-1737499 + TCGA-B5-A0JY-01 COSM1588686 c.5555C>T p.T1852I Substitution - Missense 17:1737414-1737414 + TCGA-33-4532-01 COSM1147747 c.5299G>A p.V1767M Substitution - Missense 17:1735691-1735691 + T3498 COSM4741080 c.580G>A p.V194M Substitution - Missense 17:1730445-1730445 + CSCC-20-T COSM4568961 c.1422T>C p.H474H Substitution - coding silent 17:1726381-1726381 + PT41 COSM5924699 c.722C>T p.S241F Substitution - Missense 17:1725681-1725681 + TCGA-B5-A11E-01 COSM1588608 c.732C>T p.D244D Substitution - coding silent 17:1725691-1725691 + 2492723 COSM5722512 c.990C>A p.T330T Substitution - coding silent 17:1731244-1731244 + T3080 COSM4741091 c.4887G>A p.Q1629Q Substitution - coding silent 17:1733924-1733924 + TCGA-C5-A1BI-01 COSM1381110 c.5335C>T p.R1779* Substitution - Nonsense 17:1736048-1736048 + PT13 COSM5896339 c.2027-5C>T p.? Unknown 17:1735567-1735567 + PA285 COSM1163141 c.4537C>A p.L1513M Substitution - Missense 17:1733574-1733574 + TCGA-AZ-4315-01 COSM1381097 c.4231C>T p.R1411C Substitution - Missense 17:1732398-1732398 + CN-AML-08-T COSM3932488 c.1450A>G p.M484V Substitution - Missense 17:1733640-1733640 + HCT-15 COSM1679362 c.2573C>A p.S858Y Substitution - Missense 17:1737585-1737585 + TCGA-ER-A194-01 COSM3514589 c.912C>T p.Y304Y Substitution - coding silent 17:1731166-1731166 + C135 COSM4617725 c.303C>T p.S101S Substitution - coding silent 17:1728415-1728415 + LIM2099 COSM4641094 c.1072A>G p.S358G Substitution - Missense 17:1726031-1726031 + SKCO-1 COSM4641096 c.2254C>T p.P752S Substitution - Missense 17:1727213-1727213 + TCGA-AM-5821-01 COSM436117 c.2487C>T p.S829S Substitution - coding silent 17:1737499-1737499 + TCGA-CG-5728-01 COSM4064211 c.4943C>T p.S1648L Substitution - Missense 17:1733980-1733980 + TCGA-BR-4280-01 COSM4064190 c.3889A>G p.S1297G Substitution - Missense 17:1730868-1730868 + ESO-045 COSM1270437 c.3822G>T p.P1274P Substitution - coding silent 17:1730801-1730801 + TCGA-A4-A57E-01 COSM3988793 c.2045C>T p.S682F Substitution - Missense 17:1727004-1727004 + TCGA-IK-7675-01 COSM3969849 c.1842C>T p.S614S Substitution - coding silent 17:1734032-1734032 + CSCC-29-T COSM1588688 c.5106C>T p.F1702F Substitution - coding silent 17:1734143-1734143 + 2492722 COSM5722511 c.4143C>A p.T1381T Substitution - coding silent 17:1731244-1731244 + TCGA-G4-6302-01 COSM1381084 c.3088_3090delGAG p.E1033delE Deletion - In frame 17:1728047-1728049 + TCGA-Q1-A73O-01 COSM4834279 c.992C>T p.S331F Substitution - Missense 17:1731246-1731246 + LIM2405 COSM4642078 c.662C>A p.A221D Substitution - Missense 17:1725621-1725621 + TCGA-AY-6386-01 COSM3755283 c.21G>T p.G7G Substitution - coding silent 17:1724980-1724980 + CSCC-55-T COSM4496169 c.4699C>T p.R1567C Substitution - Missense 17:1733736-1733736 + TCGA-BR-4184-01 COSM4064194 c.946C>T p.R316W Substitution - Missense 17:1731200-1731200 + T3174 COSM4741082 c.4154C>T p.T1385M Substitution - Missense 17:1731255-1731255 + CHC433T COSM1381116 c.5640C>T p.S1880S Substitution - coding silent 17:1737499-1737499 + TCGA-HE-A5NL-01 COSM3988792 c.1925C>G p.P642R Substitution - Missense 17:1726884-1726884 + RMS112_ COSM4987798 c.308C>T p.T103M Substitution - Missense 17:1725267-1725267 + TCGA-Q1-A73O-01 COSM4835081 c.1027G>T p.E343* Substitution - Nonsense 17:1725986-1725986 + TCGA-BP-5168-01 COSM1135884 c.3944A>T p.Y1315F Substitution - Missense 17:1730923-1730923 + TCGA-BR-4280-01 COSM4064191 c.736A>G p.S246G Substitution - Missense 17:1730868-1730868 + T3092 COSM4741088 c.4615G>A p.G1539R Substitution - Missense 17:1733652-1733652 + 587336 COSM1232670 c.953C>T p.P318L Substitution - Missense 17:1725912-1725912 + 61 COSM5740784 c.4724G>T p.R1575L Substitution - Missense 17:1733761-1733761 + SJRHB012_R COSM3737481 c.1297G>C p.E433Q Substitution - Missense 17:1726256-1726256 + MedB-1 COSM5622178 c.2333G>T p.G778V Substitution - Missense 17:1736199-1736199 + TCGA-DU-A5TU-01 COSM3969845 c.4450A>G p.M1484V Substitution - Missense 17:1732792-1732792 + BD87T COSM5505401 c.1357A>G p.I453V Substitution - Missense 17:1733547-1733547 + PTC-7C COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + TCGA-BP-5009-01 COSM472353 c.616T>C p.Y206H Substitution - Missense 17:1730481-1730481 + TCGA-D5-6535-01 COSM1381080 c.1542G>T p.V514V Substitution - coding silent 17:1726501-1726501 + TCGA-CG-5728-01 COSM4064212 c.1790C>T p.S597L Substitution - Missense 17:1733980-1733980 + SC_9022 COSM5561164 c.1875C>T p.N625N Substitution - coding silent 17:1726834-1726834 + pfg127T COSM4748540 c.1522T>G p.F508V Substitution - Missense 17:1733712-1733712 + TCGA-AM-5821-01 COSM1479287 c.5451A>G p.T1817T Substitution - coding silent 17:1736164-1736164 + CSCC-19-T COSM4491509 c.665C>T p.P222L Substitution - Missense 17:1730797-1730797 + PCSI_0547_Pa_P_526 COSM5031923 c.663T>C p.A221A Substitution - coding silent 17:1725622-1725622 + ESO-0129 COSM1270435 c.2114C>T p.T705I Substitution - Missense 17:1735659-1735659 + SC_9009 COSM5573840 c.1293_1294insG p.E433fs*43 Insertion - Frameshift 17:1726252-1726253 + 2171664 COSM4423110 c.1916G>A p.R639H Substitution - Missense 17:1734106-1734106 + CSCC-47-T COSM4487468 c.40C>T p.P14S Substitution - Missense 17:1728152-1728152 + HCC078T COSM5806449 c.5706G>T p.Q1902H Substitution - Missense 17:1737565-1737565 + BCB325T COSM4788529 c.2101C>A p.H701N Substitution - Missense 17:1735646-1735646 + TCGA-AM-5821-01 COSM436115 c.2298A>G p.T766T Substitution - coding silent 17:1736164-1736164 + TCGA-EE-A2MI-06 COSM3514579 c.3393C>T p.P1131P Substitution - coding silent 17:1728352-1728352 + CSCC-47-T COSM4487467 c.3193C>T p.P1065S Substitution - Missense 17:1728152-1728152 + TCGA-A6-5667-01 COSM436113 c.1974G>A p.P658P Substitution - coding silent 17:1734164-1734164 + YUMOKI COSM5385758 c.662C>T p.A221V Substitution - Missense 17:1725621-1725621 + HCT-15 COSM1679361 c.5726C>A p.S1909Y Substitution - Missense 17:1737585-1737585 + TCGA-A6-6780-01 COSM1381111 c.2182C>T p.R728* Substitution - Nonsense 17:1736048-1736048 + TCGA-AP-A0LM-01 COSM975931 c.1953C>T p.F651F Substitution - coding silent 17:1734143-1734143 + TCGA-AM-5821-01 COSM1381116 c.5640C>T p.S1880S Substitution - coding silent 17:1737499-1737499 + ESO-859 COSM1240648 c.5046C>T p.D1682D Substitution - coding silent 17:1734083-1734083 + MO_1012 COSM2739409 c.1668G>A p.P556P Substitution - coding silent 17:1733858-1733858 + PTC-14C COSM4129619 c.1486G>C p.G496R Substitution - Missense 17:1733676-1733676 + TCGA-BS-A0UF-01 COSM1588703 c.2563C>A p.L855M Substitution - Missense 17:1727522-1727522 + PTC-7C COSM4129617 c.2331A>G p.L777L Substitution - coding silent 17:1727290-1727290 + TCGA-D1-A103-01 COSM1588687 c.5231C>T p.A1744V Substitution - Missense 17:1735623-1735623 + PA285 COSM1163142 c.1384C>A p.L462M Substitution - Missense 17:1733574-1733574 + TCGA-AA-3663-01 COSM3755291 c.4971A>G p.L1657L Substitution - coding silent 17:1734008-1734008 + OSCC-GB_00580111 COSM2739457 c.2140C>T p.R714C Substitution - Missense 17:1735685-1735685 + TCGA-BH-A0BL-01 COSM1479278 c.2461G>A p.V821M Substitution - Missense 17:1727420-1727420 + 2334199 COSM324303 c.959A>T p.E320V Substitution - Missense 17:1731213-1731213 + I2L-P7-Tumor-Organoid COSM5364413 c.754G>A p.A252T Substitution - Missense 17:1730886-1730886 + B106-Tumor COSM3932487 c.4603A>G p.M1535V Substitution - Missense 17:1733640-1733640 + sysucc-1317T COSM5448940 c.1391G>A p.C464Y Substitution - Missense 17:1726350-1726350 + LUAD-NYU575 COSM375002 c.1389G>A p.A463A Substitution - coding silent 17:1733579-1733579 + TCGA-AO-A129-01 COSM1479277 c.2162T>G p.L721R Substitution - Missense 17:1727121-1727121 + TCGA-DD-A39V-01 COSM4912528 c.707T>C p.L236P Substitution - Missense 17:1730839-1730839 + PT13 COSM2739448 c.2027-4C>T p.? Unknown 17:1735568-1735568 + TCGA-AM-5821-01 COSM3755284 c.2739G>A p.L913L Substitution - coding silent 17:1727698-1727698 + CN-AML-08-T COSM3932487 c.4603A>G p.M1535V Substitution - Missense 17:1733640-1733640 + SCC-25 COSM2739421 c.1807G>A p.V603M Substitution - Missense 17:1733997-1733997 + I2L-P7-Tumor-Organoid COSM5364409 c.333C>T p.C111C Substitution - coding silent 17:1728445-1728445 + PTC-14C COSM4129618 c.4639G>C p.G1547R Substitution - Missense 17:1733676-1733676 + ZZUFHECRKL-G071T COSM5438917 c.5608G>A p.D1870N Substitution - Missense 17:1737467-1737467 + MedB-1 COSM5622175 c.1143C>G p.F381L Substitution - Missense 17:1732463-1732463 + TCGA-AP-A0LM-01 COSM1588698 c.4034C>T p.A1345V Substitution - Missense 17:1731135-1731135 + TCGA-AP-A0LM-01 COSM975922 c.881C>T p.A294V Substitution - Missense 17:1731135-1731135 + S00501 COSM5658249 c.2672G>A p.R891H Substitution - Missense 17:1727631-1727631 + LIM2551 COSM4644038 c.579C>T p.H193H Substitution - coding silent 17:1730444-1730444 + TCGA-EE-A29E-06 COSM3514576 c.131C>T p.P44L Substitution - Missense 17:1728243-1728243 + BD87T COSM5505400 c.4510A>G p.I1504V Substitution - Missense 17:1733547-1733547 + TCGA-AD-6901-01 COSM1381098 c.1078C>T p.R360C Substitution - Missense 17:1732398-1732398 + CHC433T COSM436113 c.1974G>A p.P658P Substitution - coding silent 17:1734164-1734164 + TCGA-AY-6197-01 COSM436113 c.1974G>A p.P658P Substitution - coding silent 17:1734164-1734164 + TCGA-FP-7998-01 COSM4064200 c.1186C>T p.P396S Substitution - Missense 17:1732681-1732681 + sysucc-707T COSM5460060 c.1852G>A p.G618S Substitution - Missense 17:1726811-1726811 + TCGA-DA-A1HV-06 COSM3514597 c.4574G>A p.S1525N Substitution - Missense 17:1733611-1733611 + TCGA-DU-A5TU-01 COSM3969846 c.1297A>G p.M433V Substitution - Missense 17:1732792-1732792 + C008 COSM5524186 c.2161C>T p.L721F Substitution - Missense 17:1727120-1727120 + pfg127T COSM4748539 c.4675T>G p.F1559V Substitution - Missense 17:1733712-1733712 + TARGET-30-PARGUX COSM1288957 c.2017G>T p.G673W Substitution - Missense 17:1726976-1726976 + 2492721 COSM5722512 c.990C>A p.T330T Substitution - coding silent 17:1731244-1731244 + CHC205T COSM3755284 c.2739G>A p.L913L Substitution - coding silent 17:1727698-1727698 + STC246 COSM5055250 c.887C>A p.T296K Substitution - Missense 17:1731141-1731141 + PT13 COSM2739447 c.5180-4C>T p.? Unknown 17:1735568-1735568 + T3498 COSM4741079 c.3733G>A p.V1245M Substitution - Missense 17:1730445-1730445 + LIM2099 COSM4641096 c.2254C>T p.P752S Substitution - Missense 17:1727213-1727213 + MedB-1 COSM5622173 c.3116C>G p.A1039G Substitution - Missense 17:1728075-1728075 + TCGA-Q1-A73O-01 COSM4835100 c.1465G>A p.D489N Substitution - Missense 17:1726424-1726424 + C135 COSM4617726 c.4271C>A p.P1424H Substitution - Missense 17:1732438-1732438 + CSCC-31-T COSM4500776 c.2584C>T p.R862C Substitution - Missense 17:1737596-1737596 + CSCC-31-T COSM4501485 c.589C>T p.Q197* Substitution - Nonsense 17:1725548-1725548 + ESCC_158 COSM5646680 c.1079G>A p.R360H Substitution - Missense 17:1732399-1732399 + 587342 COSM1232675 c.1865G>A p.R622H Substitution - Missense 17:1734055-1734055 + 202_T COSM3958055 c.1508G>T p.R503L Substitution - Missense 17:1726467-1726467 + TCGA-D1-A160-01 COSM1588605 c.2210C>T p.T737M Substitution - Missense 17:1727169-1727169 + TCGA-EK-A2RJ-01 COSM4832144 c.867G>A p.A289A Substitution - coding silent 17:1731121-1731121 + 587338 COSM1232671 c.1432G>A p.A478T Substitution - Missense 17:1726391-1726391 + TCGA-C5-A1BI-01 COSM1381111 c.2182C>T p.R728* Substitution - Nonsense 17:1736048-1736048 + TCGA-G3-A5SM-01 COSM4911216 c.2530C>T p.Q844* Substitution - Nonsense 17:1727489-1727489 + TCGA-AN-A0FF-01 COSM5833235 c.620_621insC p.R210fs*8 Insertion - Frameshift 17:1725579-1725580 + TCGA-BR-8078-01 COSM4064209 c.1341C>T p.D447D Substitution - coding silent 17:1733531-1733531 + HCC078T COSM5806450 c.2553G>T p.Q851H Substitution - Missense 17:1737565-1737565 + TCGA-D1-A174-01 COSM1153030 c.2721G>A p.Q907Q Substitution - coding silent 17:1727680-1727680 + TCGA-G4-6302-01 COSM3691376 c.3779C>A p.P1260H Substitution - Missense 17:1730758-1730758 + TCGA-CM-6675-01 COSM1381105 c.2062C>T p.R688W Substitution - Missense 17:1735607-1735607 + TCGA-AP-A0LM-01 COSM975924 c.997G>A p.V333I Substitution - Missense 17:1731251-1731251 + T3535 COSM2739456 c.5293C>T p.R1765C Substitution - Missense 17:1735685-1735685 + LOVO COSM2739397 c.1570C>T p.R524W Substitution - Missense 17:1733760-1733760 + tumor_4149246 COSM5950239 c.947G>A p.R316Q Substitution - Missense 17:1731201-1731201 + CSCC-31-T COSM4476757 c.2094C>T p.S698S Substitution - coding silent 17:1727053-1727053 + TCGA-29-2429-01 COSM1324141 c.1368C>A p.H456Q Substitution - Missense 17:1733558-1733558 + CHC1209T COSM4804572 c.2139G>A p.E713E Substitution - coding silent 17:1727098-1727098 + SKCO-1 COSM4641095 c.2136G>A p.G712G Substitution - coding silent 17:1727095-1727095 + HCT15 COSM2739484 c.2412G>A p.K804K Substitution - coding silent 17:1737424-1737424 + TCGA-AP-A059-01 COSM1588704 c.2481G>A p.Q827Q Substitution - coding silent 17:1727440-1727440 + TCGA-B0-4815-01 COSM1135882 c.3689G>T p.R1230L Substitution - Missense 17:1730401-1730401 + TCGA-EE-A2MR-06 COSM3514601 c.1731C>T p.S577S Substitution - coding silent 17:1733921-1733921 + tumor_4149246 COSM5950238 c.4100G>A p.R1367Q Substitution - Missense 17:1731201-1731201 + CSCC-42-T COSM4556265 c.685G>A p.E229K Substitution - Missense 17:1725644-1725644 + TCGA-BR-4201-01 COSM4064220 c.5677G>A p.V1893I Substitution - Missense 17:1737536-1737536 + STC232 COSM2739191 c.2493C>T p.P831P Substitution - coding silent 17:1727452-1727452 + HCC133T COSM1609881 c.580_584delGAAAC p.E194fs*22 Deletion - Frameshift 17:1725539-1725543 + CSCC-38-T COSM4487348 c.23C>T p.S8F Substitution - Missense 17:1728135-1728135 + 66 COSM5743806 c.5718G>T p.K1906N Substitution - Missense 17:1737577-1737577 + TCGA-A8-A09Z-01 COSM3818907 c.1488G>A p.G496G Substitution - coding silent 17:1733678-1733678 + S02376 COSM5696975 c.4861_4872del12 p.W1621_E1624delWQYE Deletion - In frame 17:1733898-1733909 + HCT15 COSM1679362 c.2573C>A p.S858Y Substitution - Missense 17:1737585-1737585 + TCGA-DK-A3WW-01 COSM3795301 c.5740G>A p.G1914S Substitution - Missense 17:1737599-1737599 + T3080 COSM1381108 c.2096delC p.H701fs*33 Deletion - Frameshift 17:1735641-1735641 + TCGA-MU-A5YI-01 COSM4855364 c.857G>A p.R286H Substitution - Missense 17:1731111-1731111 + I2L-P7-Tumor-Organoid COSM5364412 c.3907G>A p.A1303T Substitution - Missense 17:1730886-1730886 + CSCC-38-T COSM4487347 c.3176C>T p.S1059F Substitution - Missense 17:1728135-1728135 + CHC1568T COSM4800279 c.4036G>A p.V1346M Substitution - Missense 17:1731137-1731137 + TCGA-GN-A268-06 COSM3514581 c.3448G>C p.E1150Q Substitution - Missense 17:1728407-1728407 + EGC15 COSM5055253 c.1907C>T p.T636M Substitution - Missense 17:1734097-1734097 + 587376 COSM1232681 c.1036C>A p.L346M Substitution - Missense 17:1732356-1732356 + TCGA-AP-A0LM-01 COSM1588697 c.4150G>A p.V1384I Substitution - Missense 17:1731251-1731251 + TCGA-EE-A29E-06 COSM3514575 c.3284C>T p.P1095L Substitution - Missense 17:1728243-1728243 + 2492722 COSM5722512 c.990C>A p.T330T Substitution - coding silent 17:1731244-1731244 + TCGA-AP-A0LM-01 COSM975900 c.436G>A p.G146S Substitution - Missense 17:1728548-1728548 + TCGA-A6-5667-01 COSM1479286 c.5127G>A p.P1709P Substitution - coding silent 17:1734164-1734164 + B80-3 COSM1749878 c.3922G>A p.E1308K Substitution - Missense 17:1730901-1730901 + TCGA-BR-4184-01 COSM4064203 c.1249G>A p.V417M Substitution - Missense 17:1732744-1732744 + TCGA-A8-A09Z-01 COSM3818906 c.4641G>A p.G1547G Substitution - coding silent 17:1733678-1733678 + LP6005690-DNA_C01 COSM4409277 c.4689G>C p.L1563L Substitution - coding silent 17:1733726-1733726 + 2492721 COSM5722511 c.4143C>A p.T1381T Substitution - coding silent 17:1731244-1731244 + 66 COSM5743807 c.2565G>T p.K855N Substitution - Missense 17:1737577-1737577 + PTC-7C COSM3755284 c.2739G>A p.L913L Substitution - coding silent 17:1727698-1727698 + 065T COSM1730303 c.1667A>C p.K556T Substitution - Missense 17:1726626-1726626 + TCGA-AZ-4615-01 COSM3691379 c.5396G>A p.R1799H Substitution - Missense 17:1736109-1736109 + sysucc-1163T COSM5458605 c.734T>C p.V245A Substitution - Missense 17:1725693-1725693 + TCGA-BR-4201-01 COSM4064221 c.2524G>A p.V842I Substitution - Missense 17:1737536-1737536 + UPCI:SCC090 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + SNU-283 COSM2739426 c.5009G>A p.R1670H Substitution - Missense 17:1734046-1734046 + TCGA-AA-3712-01 COSM3755291 c.4971A>G p.L1657L Substitution - coding silent 17:1734008-1734008 + TCGA-F1-6177-01 COSM4064214 c.5027C>T p.P1676L Substitution - Missense 17:1734064-1734064 + SNU-C2B COSM4651283 c.2230G>T p.G744C Substitution - Missense 17:1727189-1727189 + B80-3 COSM1749879 c.769G>A p.E257K Substitution - Missense 17:1730901-1730901 + TCGA-A5-A0RA-01 COSM975935 c.2351A>G p.K784R Substitution - Missense 17:1736217-1736217 + T3080 COSM1381107 c.5249delC p.H1752fs*33 Deletion - Frameshift 17:1735641-1735641 + CRC-20T COSM5482484 c.4158-5T>C p.? Unknown 17:1732320-1732320 + CN-AML-NR-08-Dx COSM3932488 c.1450A>G p.M484V Substitution - Missense 17:1733640-1733640 + sysucc-880T COSM5462604 c.5000G>A p.S1667N Substitution - Missense 17:1734037-1734037 + TCGA-F1-6177-01 COSM4064215 c.1874C>T p.P625L Substitution - Missense 17:1734064-1734064 + ESCC_74 COSM5634724 c.1141C>T p.P381S Substitution - Missense 17:1726100-1726100 + TCGA-FU-A3TX-01 COSM4849316 c.1288G>C p.G430R Substitution - Missense 17:1726247-1726247 + TCGA-G4-6302-01 COSM1479286 c.5127G>A p.P1709P Substitution - coding silent 17:1734164-1734164 + CCK81 COSM1381107 c.5249delC p.H1752fs*33 Deletion - Frameshift 17:1735641-1735641 + 2492720 COSM5722512 c.990C>A p.T330T Substitution - coding silent 17:1731244-1731244 + CN-AML-CR-35-Dx COSM5428211 c.3528C>A p.T1176T Substitution - coding silent 17:1728487-1728487 + ESO-887 COSM1270440 c.5583C>A p.P1861P Substitution - coding silent 17:1737442-1737442 + C135 COSM4617724 c.3456C>T p.S1152S Substitution - coding silent 17:1728415-1728415 + 61 COSM5740785 c.1571G>T p.R524L Substitution - Missense 17:1733761-1733761 + 065T COSM1730302 c.1654A>G p.K552E Substitution - Missense 17:1726613-1726613 + T3092 COSM4741089 c.1462G>A p.G488R Substitution - Missense 17:1733652-1733652 + TCGA-27-1837-01 COSM3402625 c.985C>G p.L329V Substitution - Missense 17:1731239-1731239 + TCGA-AZ-4615-01 COSM3691380 c.2243G>A p.R748H Substitution - Missense 17:1736109-1736109 + SS6003111 COSM3980254 c.29G>A p.G10D Substitution - Missense 17:1724988-1724988 + PT37 COSM5921289 c.506C>T p.S169L Substitution - Missense 17:1725465-1725465 + CN-AML-NR-08-Dx COSM3932487 c.4603A>G p.M1535V Substitution - Missense 17:1733640-1733640 + CHC205T COSM436117 c.2487C>T p.S829S Substitution - coding silent 17:1737499-1737499 + SKCO-1 COSM4641097 c.2871T>C p.N957N Substitution - coding silent 17:1727830-1727830 + TCGA-33-4532-01 COSM704890 c.2146G>A p.V716M Substitution - Missense 17:1735691-1735691 + CSCC-55-T COSM4414303 c.1799C>T p.P600L Substitution - Missense 17:1726758-1726758 + TCGA-D5-6930-01 COSM1381100 c.4239A>T p.G1413G Substitution - coding silent 17:1732406-1732406 + TCGA-A6-6138-01 COSM1381094 c.4162C>T p.P1388S Substitution - Missense 17:1732329-1732329 + TCGA-AZ-6601-01 COSM975929 c.1945G>A p.V649I Substitution - Missense 17:1734135-1734135 + YUDIVI COSM5385763 c.1557C>T p.I519I Substitution - coding silent 17:1733747-1733747 + ESO-0129 COSM1270434 c.5267C>T p.T1756I Substitution - Missense 17:1735659-1735659 + TCGA-AM-5821-01 COSM3755289 c.1466C>A p.P489H Substitution - Missense 17:1733656-1733656 + SNU-C4 COSM4652824 c.1570T>C p.F524L Substitution - Missense 17:1726529-1726529 + TCGA-AD-6901-01 COSM1381097 c.4231C>T p.R1411C Substitution - Missense 17:1732398-1732398 + TCGA-Q1-A73O-01 COSM4834278 c.4145C>T p.S1382F Substitution - Missense 17:1731246-1731246 + 587238 COSM1232666 c.3829G>A p.A1277T Substitution - Missense 17:1730808-1730808 + LIM2551 COSM4644037 c.3732C>T p.H1244H Substitution - coding silent 17:1730444-1730444 + 587342 COSM1232674 c.5018G>A p.R1673H Substitution - Missense 17:1734055-1734055 + LC_S19 COSM1189355 c.1067G>T p.R356L Substitution - Missense 17:1726026-1726026 + TCGA-EK-A2GZ-01 COSM4831126 c.4683C>T p.S1561S Substitution - coding silent 17:1733720-1733720 + CSCC-19-T COSM4491508 c.3818C>T p.P1273L Substitution - Missense 17:1730797-1730797 + 2293746 COSM4606625 c.1282G>A p.G428R Substitution - Missense 17:1726241-1726241 + OSCC-GB_00580111 COSM2739456 c.5293C>T p.R1765C Substitution - Missense 17:1735685-1735685 + TCGA-AM-5821-01 COSM3755288 c.4619C>A p.P1540H Substitution - Missense 17:1733656-1733656 + TCGA-ER-A19P-06 COSM3514604 c.1751A>T p.H584L Substitution - Missense 17:1733941-1733941 + 526LT COSM4386285 c.1450A>C p.M484L Substitution - Missense 17:1733640-1733640 + CSCC-55-T COSM4496170 c.1546C>T p.R516C Substitution - Missense 17:1733736-1733736 + I2L-P7-Tumor-Organoid COSM5364408 c.3486C>T p.C1162C Substitution - coding silent 17:1728445-1728445 + T3509 COSM4741077 c.540G>T p.W180C Substitution - Missense 17:1730405-1730405 + T3174 COSM4741083 c.1001C>T p.T334M Substitution - Missense 17:1731255-1731255 + TCGA-EE-A2MC-06 COSM3514577 c.3340A>G p.T1114A Substitution - Missense 17:1728299-1728299 + ESCC_158 COSM5646679 c.4232G>A p.R1411H Substitution - Missense 17:1732399-1732399 + PTC-10C COSM4129621 c.5145T>G p.C1715W Substitution - Missense 17:1734182-1734182 + 587316 COSM1232669 c.2276C>T p.P759L Substitution - Missense 17:1727235-1727235 + CSCC-49-T COSM4517676 c.394_395CC>TT p.P132F Substitution - Missense 17:1725353-1725354 + CSCC-31-T COSM4544089 c.346G>A p.E116K Substitution - Missense 17:1728458-1728458 + I2L-P19Tb-Tumor-Organoid COSM5364182 c.4660G>A p.G1554S Substitution - Missense 17:1733697-1733697 + CSCC-31-T COSM4544088 c.3499G>A p.E1167K Substitution - Missense 17:1728458-1728458 + S02354 COSM5695565 c.1308T>C p.H436H Substitution - coding silent 17:1726267-1726267 + NCI-H835 COSM5368177 c.1868C>T p.T623M Substitution - Missense 17:1726827-1726827 + SJRHB012 COSM3737481 c.1297G>C p.E433Q Substitution - Missense 17:1726256-1726256 + TCGA-AZ-6601-01 COSM1381103 c.5098G>A p.V1700I Substitution - Missense 17:1734135-1734135 + PTC-7C COSM1381116 c.5640C>T p.S1880S Substitution - coding silent 17:1737499-1737499 + TCGA-D1-A103-01 COSM1588604 c.2434A>G p.K812E Substitution - Missense 17:1727393-1727393 + EGC3 COSM5055247 c.642_643delCA p.T215fs*72 Deletion - Frameshift 17:1730774-1730775 + TCGA-BP-5009-01 COSM1135883 c.3769T>C p.Y1257H Substitution - Missense 17:1730481-1730481 + S02376 COSM5696976 c.1708_1719del12 p.W570_E573delWQYE Deletion - In frame 17:1733898-1733909 + TCGA-EA-A78R-01 COSM4852039 c.4721C>T p.S1574F Substitution - Missense 17:1733758-1733758 + PR-02-2480 COSM248335 c.1389G>T p.A463A Substitution - coding silent 17:1733579-1733579 + TCGA-29-2429-01 COSM1324140 c.4521C>A p.H1507Q Substitution - Missense 17:1733558-1733558 + TCGA-EK-A2GZ-01 COSM4831127 c.1530C>T p.S510S Substitution - coding silent 17:1733720-1733720 + TCGA-B5-A0K9-01 COSM1153029 c.1393G>A p.G465R Substitution - Missense 17:1726352-1726352 + HCC15T COSM1609882 c.1931A>T p.E644V Substitution - Missense 17:1726890-1726890 + CSCC-6-T COSM4467606 c.1499C>T p.S500F Substitution - Missense 17:1726458-1726458 + KM12 COSM2739480 c.5519G>A p.S1840N Substitution - Missense 17:1737378-1737378 + LOVO COSM2739396 c.4723C>T p.R1575W Substitution - Missense 17:1733760-1733760 + PT13 COSM5896338 c.5180-5C>T p.? Unknown 17:1735567-1735567 + LIM2099 COSM4641097 c.2871T>C p.N957N Substitution - coding silent 17:1727830-1727830 + TCGA-B5-A11H-01 COSM1588701 c.2974A>G p.M992V Substitution - Missense 17:1727933-1727933 + TCGA-AP-A0LM-01 COSM1588688 c.5106C>T p.F1702F Substitution - coding silent 17:1734143-1734143 + PTC-10C COSM4129622 c.1992T>G p.C664W Substitution - Missense 17:1734182-1734182 + CRC-20T COSM5482485 c.1005-5T>C p.? Unknown 17:1732320-1732320 + EGC3 COSM5055246 c.3795_3796delCA p.T1266fs*72 Deletion - Frameshift 17:1730774-1730775 + TCGA-BH-A18G-01 COSM3818903 c.4390C>G p.Q1464E Substitution - Missense 17:1732732-1732732 + 587238 COSM1232667 c.676G>A p.A226T Substitution - Missense 17:1730808-1730808 + CN-AML-CR-35-Dx COSM5428212 c.375C>A p.T125T Substitution - coding silent 17:1728487-1728487 + TCGA-B5-A0JY-01 COSM1588702 c.2781C>T p.F927F Substitution - coding silent 17:1727740-1727740 + PD13620a COSM5783645 c.2822C>T p.T941M Substitution - Missense 17:1727781-1727781 + CHC1209T COSM4804572 c.2139G>A p.E713E Substitution - coding silent 17:1727098-1727098 + TCGA-27-1837-01 COSM3402624 c.4138C>G p.L1380V Substitution - Missense 17:1731239-1731239 + TCGA-A6-6138-01 COSM1381095 c.1009C>T p.P337S Substitution - Missense 17:1732329-1732329 + T2258 COSM4741095 c.1782G>A p.P594P Substitution - coding silent 17:1733972-1733972 + TCGA-BR-A4QL-01 COSM4064218 c.1937G>A p.R646H Substitution - Missense 17:1734127-1734127 + ZZUFHECRKL-G071T COSM5438918 c.2455G>A p.D819N Substitution - Missense 17:1737467-1737467 + OSCC-GB_00600111 COSM4890374 c.1332G>T p.L444L Substitution - coding silent 17:1732827-1732827 + 587234 COSM1232678 c.3211G>A p.V1071I Substitution - Missense 17:1728170-1728170 + TCGA-ER-A193-06 COSM3514607 c.1950C>T p.F650F Substitution - coding silent 17:1734140-1734140 + TCGA-G4-6588-01 COSM1381107 c.5249delC p.H1752fs*33 Deletion - Frameshift 17:1735641-1735641 + HCC15 COSM1609882 c.1931A>T p.E644V Substitution - Missense 17:1726890-1726890 + TCGA-BH-A18G-01 COSM3818904 c.1237C>G p.Q413E Substitution - Missense 17:1732732-1732732 + TCGA-MU-A5YI-01 COSM4855363 c.4010G>A p.R1337H Substitution - Missense 17:1731111-1731111 + S02256 COSM5681245 c.45G>T p.P15P Substitution - coding silent 17:1725004-1725004 + TCGA-EK-A2RJ-01 COSM4832143 c.4020G>A p.A1340A Substitution - coding silent 17:1731121-1731121 + TCGA-A4-8515-01 COSM3988795 c.3705G>A p.K1235K Substitution - coding silent 17:1730417-1730417 + TCGA-AA-3713-01 COSM1381084 c.3088_3090delGAG p.E1033delE Deletion - In frame 17:1728047-1728049 + TCGA-Q1-A73O-01 COSM4835510 c.1203G>A p.K401K Substitution - coding silent 17:1726162-1726162 + PD24209a COSM5781004 c.3638C>G p.S1213* Substitution - Nonsense 17:1728597-1728597 + TCGA-AA-3713-01 COSM436113 c.1974G>A p.P658P Substitution - coding silent 17:1734164-1734164 + TCGA-AA-3510-01 COSM1381079 c.1401C>T p.V467V Substitution - coding silent 17:1726360-1726360 + TCGA-CM-6675-01 COSM1381104 c.5215C>T p.R1739W Substitution - Missense 17:1735607-1735607 + TARGET-30-PARKAG COSM1288955 c.1085G>T p.G362V Substitution - Missense 17:1732405-1732405 + RMS2083 COSM5880892 c.5401G>A p.V1801I Substitution - Missense 17:1736114-1736114 + CHC433T COSM1479286 c.5127G>A p.P1709P Substitution - coding silent 17:1734164-1734164 + CCK81 COSM1381108 c.2096delC p.H701fs*33 Deletion - Frameshift 17:1735641-1735641 + I2L-P19Tb-Tumor-Organoid COSM5364183 c.1507G>A p.G503S Substitution - Missense 17:1733697-1733697 + BICR_22 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + CSCC-29-T COSM975931 c.1953C>T p.F651F Substitution - coding silent 17:1734143-1734143 + CHC1568T COSM4800280 c.883G>A p.V295M Substitution - Missense 17:1731137-1731137 + HCT15 COSM1679361 c.5726C>A p.S1909Y Substitution - Missense 17:1737585-1737585 + TCGA-AM-5821-01 COSM3755292 c.1818A>G p.L606L Substitution - coding silent 17:1734008-1734008 + HCT15 COSM2739483 c.5565G>A p.K1855K Substitution - coding silent 17:1737424-1737424 + TCGA-EI-6917-01 COSM3421309 c.1636G>A p.D546N Substitution - Missense 17:1726595-1726595 + CHC205T COSM1381116 c.5640C>T p.S1880S Substitution - coding silent 17:1737499-1737499 + TCGA-BR-4184-01 COSM4064193 c.4099C>T p.R1367W Substitution - Missense 17:1731200-1731200 + TCGA-AZ-4315-01 COSM1381098 c.1078C>T p.R360C Substitution - Missense 17:1732398-1732398 + TCGA-DK-A3WW-01 COSM3795302 c.2587G>A p.G863S Substitution - Missense 17:1737599-1737599 + TCGA-AX-A0J0-01 COSM1588700 c.3457G>A p.E1153K Substitution - Missense 17:1728416-1728416 + CSCC-27-T COSM4518824 c.825_826CC>TT p.R276C Substitution - Missense 17:1725784-1725785 + TCGA-BR-4184-01 COSM4064202 c.4402G>A p.V1468M Substitution - Missense 17:1732744-1732744 + TARGET-30-PARKAG COSM1288954 c.4238G>T p.G1413V Substitution - Missense 17:1732405-1732405 + TCGA-AY-6197-01 COSM1479286 c.5127G>A p.P1709P Substitution - coding silent 17:1734164-1734164 + ACINAR29 COSM1733486 c.2696G>A p.R899H Substitution - Missense 17:1727655-1727655 + TCGA-D1-A103-01 COSM975933 c.2078C>T p.A693V Substitution - Missense 17:1735623-1735623 + 0004_CRUK_PC_0004_T1_DNA COSM5422486 c.1248G>A p.T416T Substitution - coding silent 17:1726207-1726207 + MedB-1 COSM5622177 c.5486G>T p.G1829V Substitution - Missense 17:1736199-1736199 + TCGA-AA-3663-01 COSM3755292 c.1818A>G p.L606L Substitution - coding silent 17:1734008-1734008 + TCGA-AD-5900-01 COSM1381082 c.2549C>A p.P850H Substitution - Missense 17:1727508-1727508 + EV006-R7 COSM4410926 c.3379G>A p.E1127K Substitution - Missense 17:1728338-1728338 + TCGA-B5-A0JY-01 COSM975937 c.2402C>T p.T801I Substitution - Missense 17:1737414-1737414 + LIM2099 COSM4641095 c.2136G>A p.G712G Substitution - coding silent 17:1727095-1727095 + 12T COSM108173 c.2299G>A p.G767S Substitution - Missense 17:1736165-1736165 + B80-3-Tumor COSM1749879 c.769G>A p.E257K Substitution - Missense 17:1730901-1730901 + CSCC-47-T COSM4496249 c.4711C>T p.P1571S Substitution - Missense 17:1733748-1733748 + 587342 COSM1232673 c.1259C>T p.T420I Substitution - Missense 17:1726218-1726218 + B80-3-Tumor COSM1749878 c.3922G>A p.E1308K Substitution - Missense 17:1730901-1730901 + TCGA-D5-6930-01 COSM1381101 c.1086A>T p.G362G Substitution - coding silent 17:1732406-1732406 + sysucc-1370T COSM5469303 c.2362C>T p.R788W Substitution - Missense 17:1727321-1727321 + 526LT COSM4386284 c.4603A>C p.M1535L Substitution - Missense 17:1733640-1733640 + SCC-25 COSM2739420 c.4960G>A p.V1654M Substitution - Missense 17:1733997-1733997 + T3094 COSM1381103 c.5098G>A p.V1700I Substitution - Missense 17:1734135-1734135 + TCGA-AM-5821-01 COSM1381084 c.3088_3090delGAG p.E1033delE Deletion - In frame 17:1728047-1728049 + TCGA-AP-A0LM-01 COSM1588607 c.790C>A p.L264I Substitution - Missense 17:1725749-1725749 + 8016470 COSM1153029 c.1393G>A p.G465R Substitution - Missense 17:1726352-1726352 + STC252 COSM2739173 c.1281C>T p.G427G Substitution - coding silent 17:1726240-1726240 + CSCC-29-T COSM4566869 c.1843_1844GG>AT p.G615I Substitution - Missense 17:1734033-1734034 + 587234 COSM1232677 c.2782G>A p.V928M Substitution - Missense 17:1727741-1727741 + TCGA-AP-A059-01 COSM1381103 c.5098G>A p.V1700I Substitution - Missense 17:1734135-1734135 + T3080 COSM4741092 c.1734G>A p.Q578Q Substitution - coding silent 17:1733924-1733924 + TCGA-AM-5821-01 COSM3755291 c.4971A>G p.L1657L Substitution - coding silent 17:1734008-1734008 + CSCC-29-T COSM4476333 c.2060C>T p.P687L Substitution - Missense 17:1727019-1727019 + BCB325T COSM4788528 c.5254C>A p.H1752N Substitution - Missense 17:1735646-1735646 + BCB325T COSM4788529 c.2101C>A p.H701N Substitution - Missense 17:1735646-1735646 + SCC-9 COSM2739209 c.3223G>A p.D1075N Substitution - Missense 17:1728182-1728182 + T3094 COSM975929 c.1945G>A p.V649I Substitution - Missense 17:1734135-1734135 + ESO-045 COSM1270438 c.669G>T p.P223P Substitution - coding silent 17:1730801-1730801 + sysucc-880T COSM5462605 c.1847G>A p.S616N Substitution - Missense 17:1734037-1734037 + T3535 COSM2739457 c.2140C>T p.R714C Substitution - Missense 17:1735685-1735685 + TCGA-AP-A059-01 COSM975929 c.1945G>A p.V649I Substitution - Missense 17:1734135-1734135 + PD8612a COSM5796356 c.1347G>A p.T449T Substitution - coding silent 17:1726306-1726306 + STC246 COSM5055249 c.4040C>A p.T1347K Substitution - Missense 17:1731141-1731141 + 2492729 COSM5725791 c.1983G>A p.Q661Q Substitution - coding silent 17:1726942-1726942 + OSCC-GB_00820111 COSM4887354 c.1887C>T p.Y629Y Substitution - coding silent 17:1734077-1734077 + TCGA-BP-5168-01 COSM472355 c.791A>T p.Y264F Substitution - Missense 17:1730923-1730923 + CHC1568T COSM4800279 c.4036G>A p.V1346M Substitution - Missense 17:1731137-1731137 + TCGA-EE-A2MI-06 COSM3514580 c.240C>T p.P80P Substitution - coding silent 17:1728352-1728352 + CHC1568T COSM4800280 c.883G>A p.V295M Substitution - Missense 17:1731137-1731137 + TCGA-AZ-6598-01 COSM1381114 c.2191G>A p.G731S Substitution - Missense 17:1736057-1736057 + EV006-R7 COSM4410927 c.226G>A p.E76K Substitution - Missense 17:1728338-1728338 + TCGA-DK-A3WW-01 COSM3795299 c.2251G>A p.V751M Substitution - Missense 17:1736117-1736117 + CSCC-18-T COSM4454570 c.528A>C p.S176S Substitution - coding silent 17:1725487-1725487 + KM12 COSM2739481 c.2366G>A p.S789N Substitution - Missense 17:1737378-1737378 + SCC-9 COSM2739210 c.70G>A p.D24N Substitution - Missense 17:1728182-1728182 + TCGA-EE-A2MR-06 COSM3514600 c.4884C>T p.S1628S Substitution - coding silent 17:1733921-1733921 + 8034291 COSM2739475 c.2353-7G>A p.? Unknown 17:1737358-1737358 + SCC-15 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + TCGA-BR-A4QL-01 COSM4064217 c.5090G>A p.R1697H Substitution - Missense 17:1734127-1734127 + TCGA-04-1342-01 COSM111487 c.109_115delGGGCTCT p.G37fs*2 Deletion - Frameshift 17:1728221-1728227 + TCGA-EA-A78R-01 COSM4852040 c.1568C>T p.S523F Substitution - Missense 17:1733758-1733758 + C135 COSM4617727 c.1118C>A p.P373H Substitution - Missense 17:1732438-1732438 + MedB-1 COSM5622174 c.4296C>G p.F1432L Substitution - Missense 17:1732463-1732463 + DLD1 COSM1679361 c.5726C>A p.S1909Y Substitution - Missense 17:1737585-1737585 + SNU-283 COSM2739427 c.1856G>A p.R619H Substitution - Missense 17:1734046-1734046 + T2258 COSM4741094 c.4935G>A p.P1645P Substitution - coding silent 17:1733972-1733972 + TCGA-G4-6588-01 COSM1381108 c.2096delC p.H701fs*33 Deletion - Frameshift 17:1735641-1735641 + NOKSI COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + 2172 COSM5013062 c.1972G>T p.D658Y Substitution - Missense 17:1726931-1726931 + LC_C19 COSM1189356 c.1460C>A p.T487N Substitution - Missense 17:1726419-1726419 + ESCC_BICR_070T COSM5444935 c.507C>T p.I169I Substitution - coding silent 17:1728619-1728619 + 587376 COSM1232680 c.4189C>A p.L1397M Substitution - Missense 17:1732356-1732356 + TCGA-ER-A194-01 COSM3514588 c.4065C>T p.Y1355Y Substitution - coding silent 17:1731166-1731166 + C84 COSM4620031 c.2126C>A p.A709E Substitution - Missense 17:1727085-1727085 + TCGA-DD-A39V-01 COSM4912527 c.3860T>C p.L1287P Substitution - Missense 17:1730839-1730839 + T3535 COSM4741086 c.1194C>T p.G398G Substitution - coding silent 17:1732689-1732689 + PD24209a COSM5781005 c.485C>G p.S162* Substitution - Nonsense 17:1728597-1728597 + LP6005690-DNA_C01 COSM4409278 c.1536G>C p.L512L Substitution - coding silent 17:1733726-1733726 + TCGA-24-2038-01 COSM117233 c.1138G>C p.V380L Substitution - Missense 17:1732458-1732458 + TCGA-BR-8078-01 COSM4064208 c.4494C>T p.D1498D Substitution - coding silent 17:1733531-1733531 + TCGA-ER-A19P-06 COSM3514603 c.4904A>T p.H1635L Substitution - Missense 17:1733941-1733941 + PT52 COSM5940763 c.2570C>T p.P857L Substitution - Missense 17:1727529-1727529 + PTC-53C COSM5445915 c.3097_3099delGAG p.E1033delE Deletion - In frame 17:1728056-1728058 + TCGA-EJ-5527-01 COSM472351 c.536G>T p.R179L Substitution - Missense 17:1730401-1730401 + STC297 COSM2739161 c.817G>A p.A273T Substitution - Missense 17:1725776-1725776 + 8034291 COSM2739474 c.5506-7G>A p.? Unknown 17:1737358-1737358 + TCGA-EE-A2MC-06 COSM3514578 c.187A>G p.T63A Substitution - Missense 17:1728299-1728299 + TCGA-A4-8515-01 COSM3988796 c.552G>A p.K184K Substitution - coding silent 17:1730417-1730417 + SJRHB012_S COSM3737481 c.1297G>C p.E433Q Substitution - Missense 17:1726256-1726256 + TCGA-AP-A0LM-01 COSM1588606 c.1369C>T p.R457C Substitution - Missense 17:1726328-1726328 + ESO-859 COSM1240649 c.1893C>T p.D631D Substitution - coding silent 17:1734083-1734083 + Detroit_562 COSM4594542 c.2051A>C p.Q684P Substitution - Missense 17:1727010-1727010 + 2492720 COSM5722511 c.4143C>A p.T1381T Substitution - coding silent 17:1731244-1731244 + TCGA-MY-A5BD-01 COSM4855655 c.965A>G p.D322G Substitution - Missense 17:1725924-1725924 + PTC-28C COSM436117 c.2487C>T p.S829S Substitution - coding silent 17:1737499-1737499 + PTC-7C COSM4129615 c.1585C>G p.R529G Substitution - Missense 17:1726544-1726544 + Detroit_562 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + OSCC-GB_00600111 COSM4890373 c.4485G>T p.L1495L Substitution - coding silent 17:1732827-1732827 + MO_1012 COSM2739408 c.4821G>A p.P1607P Substitution - coding silent 17:1733858-1733858 + TCGA-G4-6302-01 COSM3691377 c.626C>A p.P209H Substitution - Missense 17:1730758-1730758 + T3535 COSM4741085 c.4347C>T p.G1449G Substitution - coding silent 17:1732689-1732689 + ESO-887 COSM1270441 c.2430C>A p.P810P Substitution - coding silent 17:1737442-1737442 + 587234 COSM1232679 c.58G>A p.V20I Substitution - Missense 17:1728170-1728170 + TCGA-AA-3712-01 COSM3755292 c.1818A>G p.L606L Substitution - coding silent 17:1734008-1734008 + pfg068T COSM1381083 c.2866delA p.N957fs*7 Deletion - Frameshift 17:1727825-1727825 + TCGA-GN-A268-06 COSM3514582 c.295G>C p.E99Q Substitution - Missense 17:1728407-1728407 + EGC15 COSM5055252 c.5060C>T p.T1687M Substitution - Missense 17:1734097-1734097 + UM-SCC-4 COSM4129616 c.1955C>T p.P652L Substitution - Missense 17:1726914-1726914 + S01020 COSM5664970 c.1522G>T p.D508Y Substitution - Missense 17:1726481-1726481 + ESCC_BICR_070T COSM5444934 c.3660C>T p.I1220I Substitution - coding silent 17:1728619-1728619 + TCGA-B0-4815-01 COSM472351 c.536G>T p.R179L Substitution - Missense 17:1730401-1730401 + TCGA-G4-6302-01 COSM436113 c.1974G>A p.P658P Substitution - coding silent 17:1734164-1734164 + TCGA-AA-3713-01 COSM1479286 c.5127G>A p.P1709P Substitution - coding silent 17:1734164-1734164 + pfg181T COSM4748538 c.2096G>A p.R699H Substitution - Missense 17:1727055-1727055 + 2171664 COSM4423109 c.5069G>A p.R1690H Substitution - Missense 17:1734106-1734106 + TCGA-DA-A1HV-06 COSM3514598 c.1421G>A p.S474N Substitution - Missense 17:1733611-1733611 + 03-P152 COSM4579473 c.4825A>G p.S1609G Substitution - Missense 17:1733862-1733862 + LOVO COSM2739177 c.1346C>T p.T449M Substitution - Missense 17:1726305-1726305 + TCGA-AZ-6598-01 COSM1381113 c.5344G>A p.G1782S Substitution - Missense 17:1736057-1736057 + ccRCC-23 COSM1665010 c.1090A>C p.M364L Substitution - Missense 17:1726049-1726049 + CSCC-47-T COSM4496250 c.1558C>T p.P520S Substitution - Missense 17:1733748-1733748 + TCGA-AP-A0LM-01 COSM1588699 c.3589G>A p.G1197S Substitution - Missense 17:1728548-1728548 + TCGA-ER-A193-06 COSM3514606 c.5103C>T p.F1701F Substitution - coding silent 17:1734140-1734140 + S02322 COSM5691270 c.1214G>A p.R405H Substitution - Missense 17:1726173-1726173 + TCGA-RA-A741-01 COSM4818802 c.1017C>A p.P339P Substitution - coding silent 17:1725976-1725976 + CSCC-31-T COSM4500775 c.5737C>T p.R1913C Substitution - Missense 17:1737596-1737596 + SC_9096 COSM2739165 c.1073G>A p.S358N Substitution - Missense 17:1726032-1726032 + TCGA-B1-A47N-01 COSM4414303 c.1799C>T p.P600L Substitution - Missense 17:1726758-1726758 + 2492723 COSM5722511 c.4143C>A p.T1381T Substitution - coding silent 17:1731244-1731244 + SNU-175 COSM2739207 c.3009C>T p.H1003H Substitution - coding silent 17:1727968-1727968 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.234572 17p13.3 614218 2406343|CGAP|BC092513|A/G|non-coding||3508|Validated; 1516365|dbSNP|BC092513|G/T|non-coding||3417|Validated; 1516365|dbSNP|BC114519|G/T|non-coding||2900|Validated; 1516365|dbSNP|BC114568|G/T|non-coding||2967|Validated; 1516373|dbSNP|BC092513|A/G|non-coding||3508|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.K1835R c.5504A>G 17 1639511 UCEC A G Missense p.M992V c.2974A>G 17 1631227 UCEC A G Missense p.S1297G c.3889A>G 17 1634162 STAD A T Missense p.E1371V c.4112A>T 17 1634507 SCLC A T Missense p.H1635L c.4904A>T 17 1637235 CM A T Missense p.Y1315F c.3944A>T 17 1634217 RCCC A T Synonymous p.S1932S c.5796A>T 17 1640949 LUAD C A IntronicSNV . c.4489+80C>A 17 1636205 CM C A Missense p.P1051H c.3152C>A 17 1631405 HNSC C A Missense p.P1689Q c.5066C>A 17 1637397 CM C A Synonymous p.P1861P c.5583C>A 17 1640736 ESCA C - Frameshift p.H1545Mfs*58 c.4633delC 17 1636960 RCCC C - Frameshift p.H1752Tfs*33 c.5254delC 17 1638935 STAD C - Frameshift p.N957Mfs*7 c.2865delC 17 1631115 BRCA C G Missense p.L1380V c.4138C>G 17 1634533 GBM C T IntronicSNV . c.5326-7C>T 17 1639326 CM C T Missense p.P1676L c.5027C>T 17 1637358 STAD C T Missense p.R1670C c.5008C>T 17 1637339 CM C T Missense p.R1938C c.5812C>T 17 1640965 LUAD C T Missense p.S1648L c.4943C>T 17 1637274 STAD C T Missense p.T1756I c.5267C>T 17 1638953 ESCA C T Missense p.T737M c.2210C>T 17 1630463 UCEC C T Synonymous p.D1682D c.5046C>T 17 1637377 ESCA C T Synonymous p.F1701F c.5103C>T 17 1637434 CM C T Synonymous p.P1724P c.5172C>T 17 1637503 CM C T Synonymous p.S1665S c.4995C>T 17 1637326 LGG C T Synonymous p.Y1355Y c.4065C>T 17 1634460 CM G A 3-UTRSNV . c.5823+268G>A 17 1641244 DLBCL GAG - InFrameDeletion p.E1033delE c.3097_3099delGAG 17 1631341 PRAD G A Missense p.G465R c.1393G>A 17 1629646 UCEC G A Missense p.S1525N c.4574G>A 17 1636905 CM G A Missense p.V1767M c.5299G>A 17 1638985 LUSC G A Missense p.V1893I c.5677G>A 17 1640830 STAD G A Missense p.V821M c.2461G>A 17 1630714 BRCA G A Synonymous p.L1316L c.3948G>A 17 1634221 CM G A Synonymous p.Q907Q c.2721G>A 17 1630974 UCEC G C Missense p.E1508Q c.4522G>C 17 1636853 HNSC G C Missense p.V1431L c.4291G>C 17 1635752 OV GGGCTCT - Frameshift p.G1088Mfs*2 c.3262_3268delGGGCTCT 17 1631515 OV G T Missense p.G673W c.2017G>T 17 1630270 NB G T Missense p.R1230L c.3689G>T 17 1633695 PRAD G T Missense p.R1230L c.3689G>T 17 1633695 RCCC T C Missense p.L264P c.791T>C 17 1629044 MM T C Missense p.Y1257H c.3769T>C 17 1633775 RCCC T G Missense p.L721R c.2162T>G 17 1630415 BRCA