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 10 35302690 35302690 + Missense_Mutation SNP C C G TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr10:35302690C>G c.1926G>C c.(1924-1926)atG>atC p.M642I BLCA 10 35302719 35302719 + Missense_Mutation SNP C C G TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr10:35302719C>G c.1897G>C c.(1897-1899)Gat>Cat p.D633H BLCA 10 35305141 35305141 + Missense_Mutation SNP C C G TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr10:35305141C>G c.1866G>C c.(1864-1866)atG>atC p.M622I BLCA 10 35317752 35317752 + Nonsense_Mutation SNP T T A TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr10:35317752T>A c.1603A>T c.(1603-1605)Aaa>Taa p.K535* BLCA 10 35317755 35317755 + Missense_Mutation SNP C C T TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr10:35317755C>T c.1600G>A c.(1600-1602)Gaa>Aaa p.E534K BLCA 10 35317794 35317794 + Nonsense_Mutation SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr10:35317794G>A c.1561C>T c.(1561-1563)Cag>Tag p.Q521* BLCA 10 35318557 35318557 + Silent SNP A A C TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr10:35318557A>C c.1398T>G c.(1396-1398)ggT>ggG p.G466G BLCA 10 35320243 35320243 + Missense_Mutation SNP C C A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr10:35320243C>A c.1371G>T c.(1369-1371)atG>atT p.M457I BLCA 10 35320254 35320254 + Missense_Mutation SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr10:35320254C>T c.1360G>A c.(1360-1362)Gaa>Aaa p.E454K BLCA 10 35320309 35320309 + Nonsense_Mutation SNP G G C TCGA-G2-AA3F-01A-12D-A42E-08 TCGA-G2-AA3F-10A-01D-A42H-08 g.chr10:35320309G>C c.1305C>G c.(1303-1305)taC>taG p.Y435* BLCA 10 35320464 35320464 + Silent SNP G G A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr10:35320464G>A c.1254C>T c.(1252-1254)ttC>ttT p.F418F BLCA 10 35322104 35322104 + Missense_Mutation SNP G G A TCGA-DK-A6AV-01A-12D-A30E-08 TCGA-DK-A6AV-10A-01D-A30H-08 g.chr10:35322104G>A c.1100C>T c.(1099-1101)gCg>gTg p.A367V BLCA 10 35333784 35333784 + Silent SNP T T A TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr10:35333784T>A c.519A>T c.(517-519)ggA>ggT p.G173G BLCA 10 35351949 35351949 + Missense_Mutation SNP C C G TCGA-GV-A40E-01A-12D-A23M-08 TCGA-GV-A40E-10A-01D-A23K-08 g.chr10:35351949C>G c.161G>C c.(160-162)gGa>gCa p.G54A BLCA 10 35360127 35360127 + Splice_Site SNP G G T TCGA-XF-AAMR-01A-31D-A42E-08 TCGA-XF-AAMR-10A-01D-A42H-08 g.chr10:35360127G>T c.119C>A c.(118-120)tCa>tAa p.S40* BLCA 10 35360158 35360158 + Missense_Mutation SNP C C T TCGA-BT-A20W-01A-21D-A14W-08 TCGA-BT-A20W-11A-11D-A14W-08 g.chr10:35360158C>T c.88G>A c.(88-90)Gtc>Atc p.V30I BRCA 10 35314087 35314087 + Missense_Mutation SNP G G T TCGA-OL-A5D8-01A-11D-A27P-09 TCGA-OL-A5D8-10A-01D-A27P-09 g.chr10:35314087G>T c.1657C>A c.(1657-1659)Ctt>Att p.L553I BRCA 10 35318555 35318555 + Missense_Mutation SNP T T A TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr10:35318555T>A c.1400A>T c.(1399-1401)tAt>tTt p.Y467F BRCA 10 35327850 35327850 + Frame_Shift_Del DEL T T - TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr10:35327850delT c.875delA c.(874-876)aatfs p.N292fs BRCA 10 35333605 35333605 + Splice_Site SNP C C T TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr10:35333605C>T c.e9-1 CESC 10 35328007 35328007 + Silent SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr10:35328007G>A c.718C>T c.(718-720)Cta>Tta p.L240L CESC 10 35338621 35338621 + Missense_Mutation SNP C C G TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr10:35338621C>G c.496G>C c.(496-498)Gaa>Caa p.E166Q CESC 10 35349897 35349897 + Splice_Site SNP C C T TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr10:35349897C>T c.e5-1 CHOL 10 35327979 35327979 + Missense_Mutation SNP C C T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr10:35327979C>T c.746G>A c.(745-747)cGa>cAa p.R249Q COAD 10 35317783 35317783 + Silent SNP T T A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:35317783T>A c.1572A>T c.(1570-1572)tcA>tcT p.S524S COAD 10 35317785 35317785 + Missense_Mutation SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr10:35317785A>G c.1570T>C c.(1570-1572)Tca>Cca p.S524P COAD 10 35317808 35317808 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:35317808G>A c.1547C>T c.(1546-1548)gCg>gTg p.A516V COAD 10 35320266 35320266 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:35320266A>C c.1348T>G c.(1348-1350)Tct>Gct p.S450A COAD 10 35320266 35320266 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:35320266A>G c.1348T>C c.(1348-1350)Tct>Cct p.S450P COAD 10 35320289 35320289 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:35320289C>T c.1325G>A c.(1324-1326)cGt>cAt p.R442H COAD 10 35320547 35320547 + Splice_Site SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr10:35320547G>A c.1171C>T c.(1171-1173)Ctt>Ttt p.L391F COAD 10 35322103 35322103 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr10:35322103C>T c.1101G>A c.(1099-1101)gcG>gcA p.A367A COAD 10 35327850 35327850 + Frame_Shift_Del DEL T T - TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr10:35327850delT c.875delA c.(874-876)aatfs p.N292fs COAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COAD 10 35328011 35328011 + Splice_Site SNP C C A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr10:35328011C>A c.e10-1 COAD 10 35349819 35349819 + Nonsense_Mutation SNP A A T TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr10:35349819A>T c.300T>A c.(298-300)taT>taA p.Y100* COAD 10 35351915 35351916 + Frame_Shift_Ins INS - - A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr10:35351915_35351916insA c.194_195insT c.(193-195)ttgfs p.L65fs COAD 10 35351916 35351916 + Frame_Shift_Del DEL A A - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr10:35351916delA c.194delT c.(193-195)ttgfs p.L65fs COAD 10 35351982 35351982 + Missense_Mutation SNP T T C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr10:35351982T>C c.128A>G c.(127-129)tAt>tGt p.Y43C COADREAD 10 35317783 35317783 + Silent SNP T T A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:35317783T>A c.1572A>T c.(1570-1572)tcA>tcT p.S524S COADREAD 10 35317785 35317785 + Missense_Mutation SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr10:35317785A>G c.1570T>C c.(1570-1572)Tca>Cca p.S524P COADREAD 10 35317808 35317808 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:35317808G>A c.1547C>T c.(1546-1548)gCg>gTg p.A516V COADREAD 10 35320266 35320266 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:35320266A>C c.1348T>G c.(1348-1350)Tct>Gct p.S450A COADREAD 10 35320266 35320266 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:35320266A>G c.1348T>C c.(1348-1350)Tct>Cct p.S450P COADREAD 10 35320289 35320289 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:35320289C>T c.1325G>A c.(1324-1326)cGt>cAt p.R442H COADREAD 10 35320547 35320547 + Splice_Site SNP G G A TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr10:35320547G>A c.1171C>T c.(1171-1173)Ctt>Ttt p.L391F COADREAD 10 35322103 35322103 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr10:35322103C>T c.1101G>A c.(1099-1101)gcG>gcA p.A367A COADREAD 10 35327850 35327850 + Frame_Shift_Del DEL T T - TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr10:35327850delT c.875delA c.(874-876)aatfs p.N292fs COADREAD 10 35327979 35327979 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:35327979C>T c.746G>A c.(745-747)cGa>cAa p.R249Q COADREAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COADREAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COADREAD 10 35327980 35327980 + Nonsense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:35327980G>A c.745C>T c.(745-747)Cga>Tga p.R249* COADREAD 10 35328011 35328011 + Splice_Site SNP C C A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr10:35328011C>A c.e10-1 COADREAD 10 35349819 35349819 + Nonsense_Mutation SNP A A T TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr10:35349819A>T c.300T>A c.(298-300)taT>taA p.Y100* COADREAD 10 35351915 35351916 + Frame_Shift_Ins INS - - A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr10:35351915_35351916insA c.194_195insT c.(193-195)ttgfs p.L65fs COADREAD 10 35351916 35351916 + Frame_Shift_Del DEL A A - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr10:35351916delA c.194delT c.(193-195)ttgfs p.L65fs COADREAD 10 35351982 35351982 + Missense_Mutation SNP T T C TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr10:35351982T>C c.128A>G c.(127-129)tAt>tGt p.Y43C ESCA 10 35360127 35360127 + Splice_Site SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr10:35360127G>A c.119C>T c.(118-120)tCa>tTa p.S40L GBM 10 35299303 35299303 + Missense_Mutation SNP A A T TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr10:35299303A>T c.2174T>A c.(2173-2175)cTg>cAg p.L725Q GBMLGG 10 35299303 35299303 + Missense_Mutation SNP A A T TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr10:35299303A>T c.2174T>A c.(2173-2175)cTg>cAg p.L725Q GBMLGG 10 35320290 35320290 + Missense_Mutation SNP G G A TCGA-S9-A6U0-01A-12D-A32B-08 TCGA-S9-A6U0-10A-01D-A329-08 g.chr10:35320290G>A c.1324C>T c.(1324-1326)Cgt>Tgt p.R442C GBMLGG 10 35322128 35322128 + Missense_Mutation SNP T T G TCGA-TM-A84H-01A-11D-A36O-08 TCGA-TM-A84H-10A-01D-A367-08 g.chr10:35322128T>G c.1076A>C c.(1075-1077)aAt>aCt p.N359T GBMLGG 10 35324207 35324207 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chr10:35324207C>T c.895G>A c.(895-897)Gtc>Atc p.V299I GBMLGG 10 35324208 35324208 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35324208G>A c.894C>T c.(892-894)taC>taT p.Y298Y GBMLGG 10 35327937 35327937 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35327937A>C c.788T>G c.(787-789)aTt>aGt p.I263S GBMLGG 10 35333549 35333549 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35333549T>G c.659A>C c.(658-660)aAa>aCa p.K220T GBMLGG 10 35351961 35351961 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35351961G>T c.149C>A c.(148-150)cCt>cAt p.P50H HNSC 10 35299242 35299242 + Silent SNP C C T TCGA-QK-A8Z9-01B-11D-A391-08 TCGA-QK-A8Z9-10A-01D-A394-08 g.chr10:35299242C>T c.2235G>A c.(2233-2235)gcG>gcA p.A745A HNSC 10 35327992 35327992 + Missense_Mutation SNP C C G TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr10:35327992C>G c.733G>C c.(733-735)Gat>Cat p.D245H HNSC 10 35351986 35351986 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:35351986T>C c.124A>G c.(124-126)Atc>Gtc p.I42V HNSC 10 35360215 35360215 + Missense_Mutation SNP C C G TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr10:35360215C>G c.31G>C c.(31-33)Gat>Cat p.D11H KICH 10 35320289 35320289 + Missense_Mutation SNP C C T TCGA-KN-8429-01A-11D-2310-10 TCGA-KN-8429-11A-01D-2311-10 g.chr10:35320289C>T c.1325G>A c.(1324-1326)cGt>cAt p.R442H KICH 10 35333504 35333504 + Missense_Mutation SNP T T C TCGA-KM-8476-01A-11D-2310-10 TCGA-KM-8476-10A-01D-2311-10 g.chr10:35333504T>C c.704A>G c.(703-705)tAt>tGt p.Y235C KIPAN 10 35299283 35299283 + Missense_Mutation SNP C C T TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr10:35299283C>T c.2194G>A c.(2194-2196)Gaa>Aaa p.E732K KIPAN 10 35320289 35320289 + Missense_Mutation SNP C C T TCGA-KN-8429-01A-11D-2310-10 TCGA-KN-8429-11A-01D-2311-10 g.chr10:35320289C>T c.1325G>A c.(1324-1326)cGt>cAt p.R442H KIPAN 10 35324145 35324145 + Silent SNP G G T TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chr10:35324145G>T c.957C>A c.(955-957)atC>atA p.I319I KIPAN 10 35333504 35333504 + Missense_Mutation SNP T T C TCGA-KM-8476-01A-11D-2310-10 TCGA-KM-8476-10A-01D-2311-10 g.chr10:35333504T>C c.704A>G c.(703-705)tAt>tGt p.Y235C KIPAN 10 35360197 35360197 + Missense_Mutation SNP G G C TCGA-Q2-A5QZ-01A-11D-A28G-10 TCGA-Q2-A5QZ-10A-01D-A28G-10 g.chr10:35360197G>C c.49C>G c.(49-51)Ctt>Gtt p.L17V KIRC 10 35299283 35299283 + Missense_Mutation SNP C C T TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr10:35299283C>T c.2194G>A c.(2194-2196)Gaa>Aaa p.E732K KIRP 10 35324145 35324145 + Silent SNP G G T TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chr10:35324145G>T c.957C>A c.(955-957)atC>atA p.I319I KIRP 10 35360197 35360197 + Missense_Mutation SNP G G C TCGA-Q2-A5QZ-01A-11D-A28G-10 TCGA-Q2-A5QZ-10A-01D-A28G-10 g.chr10:35360197G>C c.49C>G c.(49-51)Ctt>Gtt p.L17V LGG 10 35320290 35320290 + Missense_Mutation SNP G G A TCGA-S9-A6U0-01A-12D-A32B-08 TCGA-S9-A6U0-10A-01D-A329-08 g.chr10:35320290G>A c.1324C>T c.(1324-1326)Cgt>Tgt p.R442C LGG 10 35322128 35322128 + Missense_Mutation SNP T T G TCGA-TM-A84H-01A-11D-A36O-08 TCGA-TM-A84H-10A-01D-A367-08 g.chr10:35322128T>G c.1076A>C c.(1075-1077)aAt>aCt p.N359T LGG 10 35324207 35324207 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chr10:35324207C>T c.895G>A c.(895-897)Gtc>Atc p.V299I LGG 10 35324208 35324208 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35324208G>A c.894C>T c.(892-894)taC>taT p.Y298Y LGG 10 35327937 35327937 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35327937A>C c.788T>G c.(787-789)aTt>aGt p.I263S LGG 10 35333549 35333549 + Missense_Mutation SNP T T G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35333549T>G c.659A>C c.(658-660)aAa>aCa p.K220T LGG 10 35351961 35351961 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:35351961G>T c.149C>A c.(148-150)cCt>cAt p.P50H LIHC 10 35320492 35320492 + Missense_Mutation SNP T T C TCGA-2Y-A9H5-01A-11D-A382-10 TCGA-2Y-A9H5-10A-01D-A385-10 g.chr10:35320492T>C c.1226A>G c.(1225-1227)aAt>aGt p.N409S LIHC 10 35328009 35328009 + Splice_Site SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:35328009A>G c.716T>C c.(715-717)gTt>gCt p.V239A LIHC 10 35333758 35333758 + Missense_Mutation SNP T T C TCGA-QA-A7B7-01A-11D-A32G-10 TCGA-QA-A7B7-10A-01D-A32G-10 g.chr10:35333758T>C c.545A>G c.(544-546)cAt>cGt p.H182R LUAD 10 35300818 35300818 + Missense_Mutation SNP C C A TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr10:35300818C>A c.2064G>T c.(2062-2064)atG>atT p.M688I LUAD 10 35318521 35318521 + Silent SNP T T C TCGA-86-8673-01A-11D-2393-08 TCGA-86-8673-10A-01D-2393-08 g.chr10:35318521T>C c.1434A>G c.(1432-1434)acA>acG p.T478T LUAD 10 35320243 35320243 + Missense_Mutation SNP C C G TCGA-73-4676-01A-01D-1753-08 TCGA-73-4676-11A-01D-1753-08 g.chr10:35320243C>G c.1371G>C c.(1369-1371)atG>atC p.M457I LUAD 10 35321407 35321407 + Missense_Mutation SNP C C A TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr10:35321407C>A c.1126G>T c.(1126-1128)Gta>Tta p.V376L LUAD 10 35327986 35327986 + Nonsense_Mutation SNP C C A TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr10:35327986C>A c.739G>T c.(739-741)Gaa>Taa p.E247* LUAD 10 35333508 35333508 + Nonsense_Mutation SNP G G A TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr10:35333508G>A c.700C>T c.(700-702)Cag>Tag p.Q234* LUAD 10 35333791 35333791 + Missense_Mutation SNP C C A TCGA-35-4123-01A-01D-1105-08 TCGA-35-4123-10A-01D-1105-08 g.chr10:35333791C>A c.512G>T c.(511-513)cGt>cTt p.R171L LUAD 10 35333797 35333797 + Splice_Site SNP C C A TCGA-35-4123-01A-01D-1105-08 TCGA-35-4123-10A-01D-1105-08 g.chr10:35333797C>A c.e8-1 LUAD 10 35349836 35349836 + Missense_Mutation SNP T T A TCGA-49-6744-01A-11D-1855-08 TCGA-49-6744-11A-01D-1855-08 g.chr10:35349836T>A c.283A>T c.(283-285)Agc>Tgc p.S95C LUSC 10 35324157 35324157 + Silent SNP C C T TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr10:35324157C>T c.945G>A c.(943-945)ctG>ctA p.L315L LUSC 10 35333790 35333790 + Silent SNP A A C TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chr10:35333790A>C c.513T>G c.(511-513)cgT>cgG p.R171R OV 10 35317783 35317783 + Silent SNP T T C TCGA-61-2008-01A-02W-0722-08 TCGA-61-2008-11A-01W-0722-08 g.chr10:35317783T>C c.1572A>G c.(1570-1572)tcA>tcG p.S524S OV 10 35328011 35328011 + Splice_Site SNP C C T TCGA-13-0893-01B-01W-0494-09 TCGA-13-0893-10A-01W-0494-09 g.chr10:35328011C>T c.e10-1 OV 10 35349820 35349820 + Missense_Mutation SNP T T C TCGA-24-2267-01A-01W-0799-08 TCGA-24-2267-11A-01W-0799-08 g.chr10:35349820T>C c.299A>G c.(298-300)tAt>tGt p.Y100C PAAD 10 35317808 35317808 + Missense_Mutation SNP G G A TCGA-HZ-A77P-01A-11D-A33T-08 TCGA-HZ-A77P-10A-01D-A33W-08 g.chr10:35317808G>A c.1547C>T c.(1546-1548)gCg>gTg p.A516V PAAD 10 35327850 35327850 + Frame_Shift_Del DEL T T - TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr10:35327850delT c.875delA c.(874-876)aatfs p.N292fs PRAD 10 35305223 35305223 + Missense_Mutation SNP C C G TCGA-KK-A8I9-01A-11D-A364-08 TCGA-KK-A8I9-11A-11D-A362-08 g.chr10:35305223C>G c.1784G>C c.(1783-1785)aGt>aCt p.S595T PRAD 10 35318439 35318439 + Missense_Mutation SNP T T G TCGA-KK-A59Z-01A-12D-A26M-08 TCGA-KK-A59Z-11A-11D-A26K-08 g.chr10:35318439T>G c.1516A>C c.(1516-1518)Agt>Cgt p.S506R PRAD 10 35322104 35322104 + Missense_Mutation SNP G G A TCGA-YL-A9WX-01A-21D-A41K-08 TCGA-YL-A9WX-10A-01D-A41N-08 g.chr10:35322104G>A c.1100C>T c.(1099-1101)gCg>gTg p.A367V PRAD 10 35351967 35351967 + Missense_Mutation SNP G G A TCGA-EJ-5494-01A-01D-1576-08 TCGA-EJ-5494-10A-01D-1577-08 g.chr10:35351967G>A c.143C>T c.(142-144)gCc>gTc p.A48V READ 10 35327979 35327979 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:35327979C>T c.746G>A c.(745-747)cGa>cAa p.R249Q SKCM 10 35324198 35324198 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:35324198G>A c.904C>T c.(904-906)Cgt>Tgt p.R302C SKCM 10 35328007 35328007 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:35328007G>A c.718C>T c.(718-720)Cta>Tta p.L240L SKCM 10 35333706 35333706 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:35333706G>A c.597C>T c.(595-597)ccC>ccT p.P199P SKCM 10 35333707 35333707 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:35333707G>A c.596C>T c.(595-597)cCc>cTc p.P199L SKCM 10 35343418 35343418 + Missense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr10:35343418G>A c.367C>T c.(367-369)Ctt>Ttt p.L123F SKCM 10 35343419 35343419 + Silent SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr10:35343419G>A c.366C>T c.(364-366)gaC>gaT p.D122D SKCM 10 35349802 35349802 + Splice_Site SNP C C T TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chr10:35349802C>T c.317G>A c.(316-318)aGg>aAg p.R106K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 10 35317752 35317752 single base substitution T A 3_prime_UTR_variant BLCA-US 10 35317752 35317752 single base substitution T A stop_gained K478* 1432A>T BLCA-US 10 35317752 35317752 single base substitution T A stop_gained K535* 1603A>T BLCA-US 10 35317752 35317752 single base substitution T A stop_gained K554* 1660A>T BLCA-US 10 35317794 35317794 single base substitution G A 3_prime_UTR_variant BLCA-US 10 35317794 35317794 single base substitution G A stop_gained Q464* 1390C>T BLCA-US 10 35317794 35317794 single base substitution G A stop_gained Q521* 1561C>T BLCA-US 10 35317794 35317794 single base substitution G A stop_gained Q540* 1618C>T BLCA-US 10 35351949 35351949 single base substitution C G downstream_gene_variant BLCA-US 10 35351949 35351949 single base substitution C G exon_variant BLCA-US 10 35351949 35351949 single base substitution C G missense_variant E12Q 34G>C BLCA-US 10 35351949 35351949 single base substitution C G missense_variant G54A 161G>C BLCA-US 10 35351949 35351949 single base substitution C G missense_variant G73A 218G>C BLCA-US 10 35360158 35360158 single base substitution C T 5_prime_UTR_variant BLCA-US 10 35360158 35360158 single base substitution C T exon_variant BLCA-US 10 35360158 35360158 single base substitution C T missense_variant V30I 88G>A BLCA-US 10 35360158 35360158 single base substitution C T missense_variant V49I 145G>A BOCA-FR 10 35360945 35360945 single base substitution G A intron_variant BOCA-FR 10 35360945 35360945 single base substitution G A upstream_gene_variant BRCA-EU 10 35293949 35293949 single base substitution C T downstream_gene_variant BRCA-EU 10 35294617 35294619 deletion of <=200bp GAG - downstream_gene_variant BRCA-EU 10 35294748 35294748 single base substitution T C downstream_gene_variant BRCA-EU 10 35295018 35295018 single base substitution C T downstream_gene_variant BRCA-EU 10 35297152 35297152 single base substitution G C downstream_gene_variant BRCA-EU 10 35297514 35297514 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 35297514 35297514 single base substitution C G downstream_gene_variant BRCA-EU 10 35299089 35299089 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 35299089 35299089 single base substitution C T downstream_gene_variant BRCA-EU 10 35299362 35299362 insertion of <=200bp - GCT 3_prime_UTR_variant BRCA-EU 10 35299362 35299362 insertion of <=200bp - GCT inframe_insertion S648SS BRCA-EU 10 35299362 35299362 insertion of <=200bp - GCT inframe_insertion S666SS BRCA-EU 10 35299362 35299362 insertion of <=200bp - GCT inframe_insertion S705SS BRCA-EU 10 35299362 35299362 insertion of <=200bp - GCT inframe_insertion S724SS BRCA-EU 10 35303163 35303163 single base substitution C A intron_variant BRCA-EU 10 35303392 35303392 single base substitution C G intron_variant BRCA-EU 10 35306362 35306362 single base substitution C A intron_variant BRCA-EU 10 35306797 35306797 single base substitution C T intron_variant BRCA-EU 10 35308470 35308470 single base substitution T C intron_variant BRCA-EU 10 35310109 35310109 single base substitution T C intron_variant BRCA-EU 10 35311011 35311011 single base substitution C G intron_variant BRCA-EU 10 35313540 35313540 single base substitution T A intron_variant BRCA-EU 10 35314142 35314142 single base substitution A C intron_variant BRCA-EU 10 35314963 35314963 single base substitution C G intron_variant BRCA-EU 10 35316471 35316471 single base substitution T G intron_variant BRCA-EU 10 35317106 35317106 single base substitution C A intron_variant BRCA-EU 10 35319304 35319304 deletion of <=200bp T - intron_variant BRCA-EU 10 35321016 35321016 deletion of <=200bp A - intron_variant BRCA-EU 10 35321344 35321344 single base substitution C T intron_variant BRCA-EU 10 35322533 35322533 single base substitution C T intron_variant BRCA-EU 10 35323311 35323311 single base substitution T A intron_variant BRCA-EU 10 35326464 35326464 single base substitution G C intron_variant BRCA-EU 10 35326888 35326888 single base substitution G A intron_variant BRCA-EU 10 35327701 35327701 single base substitution C G intron_variant BRCA-EU 10 35327842 35327845 deletion of <=200bp ACTT - splice_region_variant BRCA-EU 10 35329154 35329154 single base substitution C G downstream_gene_variant BRCA-EU 10 35329154 35329154 single base substitution C G intron_variant BRCA-EU 10 35331673 35331673 single base substitution T C downstream_gene_variant BRCA-EU 10 35331673 35331673 single base substitution T C intron_variant BRCA-EU 10 35332728 35332728 single base substitution C A downstream_gene_variant BRCA-EU 10 35332728 35332728 single base substitution C A intron_variant BRCA-EU 10 35333494 35333494 single base substitution C A downstream_gene_variant BRCA-EU 10 35333494 35333494 single base substitution C A missense_variant K181N 543G>T BRCA-EU 10 35333494 35333494 single base substitution C A missense_variant K238N 714G>T BRCA-EU 10 35333494 35333494 single base substitution C A missense_variant K257N 771G>T BRCA-EU 10 35333494 35333494 single base substitution C A splice_region_variant BRCA-EU 10 35336976 35336976 single base substitution G C intron_variant BRCA-EU 10 35339967 35339967 single base substitution G C intron_variant BRCA-EU 10 35340669 35340669 single base substitution A C intron_variant BRCA-EU 10 35340701 35340701 single base substitution T G intron_variant BRCA-EU 10 35341043 35341043 single base substitution C A intron_variant BRCA-EU 10 35341945 35341945 deletion of <=200bp A - intron_variant BRCA-EU 10 35341945 35341945 insertion of <=200bp - A intron_variant BRCA-EU 10 35342946 35342946 single base substitution C G intron_variant BRCA-EU 10 35346739 35346739 single base substitution G A downstream_gene_variant BRCA-EU 10 35346739 35346739 single base substitution G A intron_variant BRCA-EU 10 35347863 35347863 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 35347863 35347863 deletion of <=200bp A - intron_variant BRCA-EU 10 35348327 35348327 single base substitution C T downstream_gene_variant BRCA-EU 10 35348327 35348327 single base substitution C T intron_variant BRCA-EU 10 35348474 35348474 single base substitution C T downstream_gene_variant BRCA-EU 10 35348474 35348474 single base substitution C T intron_variant BRCA-EU 10 35350787 35350787 single base substitution C T downstream_gene_variant BRCA-EU 10 35350787 35350787 single base substitution C T intron_variant BRCA-EU 10 35351295 35351295 single base substitution C A downstream_gene_variant BRCA-EU 10 35351295 35351295 single base substitution C A intron_variant BRCA-EU 10 35353023 35353023 single base substitution C T exon_variant BRCA-EU 10 35353023 35353023 single base substitution C T intron_variant BRCA-EU 10 35353308 35353308 single base substitution C G intron_variant BRCA-EU 10 35354581 35354581 single base substitution A C intron_variant BRCA-EU 10 35354893 35354895 deletion of <=200bp CTC - intron_variant BRCA-EU 10 35354977 35354977 single base substitution A G intron_variant BRCA-EU 10 35355077 35355077 single base substitution T A intron_variant BRCA-EU 10 35355150 35355150 single base substitution A T intron_variant BRCA-EU 10 35355190 35355190 single base substitution A T intron_variant BRCA-EU 10 35357818 35357818 single base substitution G A intron_variant BRCA-EU 10 35358157 35358157 single base substitution C G intron_variant BRCA-EU 10 35358310 35358310 single base substitution A T intron_variant BRCA-EU 10 35358783 35358783 single base substitution C A intron_variant BRCA-EU 10 35358908 35358908 single base substitution T C intron_variant BRCA-EU 10 35360413 35360413 single base substitution A T intron_variant BRCA-EU 10 35360413 35360413 single base substitution A T upstream_gene_variant BRCA-EU 10 35361592 35361592 single base substitution G A intron_variant BRCA-EU 10 35361592 35361592 single base substitution G A upstream_gene_variant BRCA-EU 10 35361771 35361771 single base substitution C T intron_variant BRCA-EU 10 35361771 35361771 single base substitution C T upstream_gene_variant BRCA-EU 10 35364410 35364410 single base substitution C T intron_variant BRCA-EU 10 35364410 35364410 single base substitution C T upstream_gene_variant BRCA-EU 10 35366013 35366013 single base substitution C G intron_variant BRCA-EU 10 35366013 35366013 single base substitution C G upstream_gene_variant BRCA-EU 10 35366418 35366418 single base substitution C G intron_variant BRCA-EU 10 35366418 35366418 single base substitution C G upstream_gene_variant BRCA-EU 10 35368153 35368153 single base substitution C T intron_variant BRCA-EU 10 35368153 35368153 single base substitution C T upstream_gene_variant BRCA-EU 10 35369342 35369342 single base substitution C A intron_variant BRCA-EU 10 35370836 35370836 single base substitution G A intron_variant BRCA-EU 10 35373360 35373360 single base substitution C T intron_variant BRCA-EU 10 35373728 35373728 single base substitution G C intron_variant BRCA-EU 10 35374048 35374048 deletion of <=200bp A - intron_variant BRCA-EU 10 35375692 35375692 single base substitution C A intron_variant BRCA-EU 10 35375709 35375709 single base substitution G A intron_variant BRCA-EU 10 35375806 35375806 single base substitution C G intron_variant BRCA-EU 10 35379273 35379273 single base substitution G A 5_prime_UTR_variant BRCA-EU 10 35379273 35379273 single base substitution G A intron_variant BRCA-EU 10 35379273 35379273 single base substitution G A upstream_gene_variant BRCA-EU 10 35379525 35379525 single base substitution C T 5_prime_UTR_variant BRCA-EU 10 35379525 35379525 single base substitution C T upstream_gene_variant BRCA-EU 10 35380814 35380814 single base substitution C A upstream_gene_variant BRCA-EU 10 35381624 35381624 single base substitution C A upstream_gene_variant BRCA-EU 10 35382060 35382060 single base substitution C G upstream_gene_variant BRCA-EU 10 35382204 35382204 single base substitution T G upstream_gene_variant BRCA-EU 10 35382506 35382506 deletion of <=200bp G - upstream_gene_variant BRCA-EU 10 35382703 35382703 single base substitution C G upstream_gene_variant BRCA-EU 10 35382722 35382722 single base substitution C G upstream_gene_variant BRCA-EU 10 35384010 35384010 single base substitution G A upstream_gene_variant BRCA-EU 10 35384303 35384303 single base substitution C G upstream_gene_variant BRCA-FR 10 35299603 35299603 single base substitution A G intron_variant BRCA-FR 10 35303392 35303392 single base substitution C G intron_variant BRCA-FR 10 35307659 35307659 single base substitution C T intron_variant BRCA-FR 10 35307920 35307920 single base substitution A T intron_variant BRCA-FR 10 35322533 35322533 single base substitution C T intron_variant BRCA-FR 10 35326809 35326809 single base substitution C T intron_variant BRCA-FR 10 35327701 35327701 single base substitution C G intron_variant BRCA-FR 10 35329154 35329154 single base substitution C G downstream_gene_variant BRCA-FR 10 35329154 35329154 single base substitution C G intron_variant BRCA-FR 10 35348327 35348327 single base substitution C T downstream_gene_variant BRCA-FR 10 35348327 35348327 single base substitution C T intron_variant BRCA-FR 10 35355077 35355077 single base substitution T A intron_variant BRCA-FR 10 35360413 35360413 single base substitution A T intron_variant BRCA-FR 10 35360413 35360413 single base substitution A T upstream_gene_variant BRCA-FR 10 35361592 35361592 single base substitution G A intron_variant BRCA-FR 10 35361592 35361592 single base substitution G A upstream_gene_variant BRCA-FR 10 35366418 35366418 single base substitution C G intron_variant BRCA-FR 10 35366418 35366418 single base substitution C G upstream_gene_variant BRCA-FR 10 35373728 35373728 single base substitution G C intron_variant BRCA-FR 10 35375806 35375806 single base substitution C G intron_variant BRCA-FR 10 35379525 35379525 single base substitution C T 5_prime_UTR_variant BRCA-FR 10 35379525 35379525 single base substitution C T upstream_gene_variant BRCA-FR 10 35382060 35382060 single base substitution C G upstream_gene_variant BRCA-FR 10 35384303 35384303 single base substitution C G upstream_gene_variant BRCA-UK 10 35299700 35299700 single base substitution C T intron_variant BRCA-UK 10 35318485 35318485 single base substitution G C 3_prime_UTR_variant BRCA-UK 10 35318485 35318485 single base substitution G C missense_variant F433L 1299C>G BRCA-UK 10 35318485 35318485 single base substitution G C missense_variant F490L 1470C>G BRCA-UK 10 35318485 35318485 single base substitution G C missense_variant F509L 1527C>G BRCA-UK 10 35326464 35326464 single base substitution G C intron_variant BRCA-UK 10 35348474 35348474 single base substitution C T downstream_gene_variant BRCA-UK 10 35348474 35348474 single base substitution C T intron_variant BRCA-UK 10 35358783 35358783 single base substitution C A intron_variant BRCA-UK 10 35380276 35380276 single base substitution C G upstream_gene_variant BRCA-US 10 35314087 35314087 single base substitution G T 3_prime_UTR_variant BRCA-US 10 35314087 35314087 single base substitution G T missense_variant L496I 1486C>A BRCA-US 10 35314087 35314087 single base substitution G T missense_variant L553I 1657C>A BRCA-US 10 35314087 35314087 single base substitution G T missense_variant L572I 1714C>A BRCA-US 10 35318555 35318555 single base substitution T A 3_prime_UTR_variant BRCA-US 10 35318555 35318555 single base substitution T A missense_variant Y410F 1229A>T BRCA-US 10 35318555 35318555 single base substitution T A missense_variant Y467F 1400A>T BRCA-US 10 35318555 35318555 single base substitution T A missense_variant Y486F 1457A>T BRCA-US 10 35327850 35327850 deletion of <=200bp T - frameshift_variant N235 BRCA-US 10 35327850 35327850 deletion of <=200bp T - frameshift_variant N292 BRCA-US 10 35327850 35327850 deletion of <=200bp T - frameshift_variant N311 BRCA-US 10 35327850 35327850 deletion of <=200bp T - splice_region_variant BRCA-US 10 35333605 35333605 single base substitution C T splice_acceptor_variant BTCA-JP 10 35327840 35327840 single base substitution T C splice_region_variant BTCA-JP 10 35328015 35328015 deletion of <=200bp A - splice_region_variant BTCA-JP 10 35338759 35338759 insertion of <=200bp - T intron_variant BTCA-JP 10 35351915 35351915 single base substitution C A downstream_gene_variant BTCA-JP 10 35351915 35351915 single base substitution C A exon_variant BTCA-JP 10 35351915 35351915 single base substitution C A missense_variant L65F 195G>T BTCA-JP 10 35351915 35351915 single base substitution C A missense_variant L84F 252G>T BTCA-JP 10 35351915 35351915 single base substitution C A missense_variant W23L 68G>T CESC-US 10 35328007 35328007 single base substitution G A 3_prime_UTR_variant CESC-US 10 35328007 35328007 single base substitution G A synonymous_variant L183L 547C>T CESC-US 10 35328007 35328007 single base substitution G A synonymous_variant L240L 718C>T CESC-US 10 35328007 35328007 single base substitution G A synonymous_variant L259L 775C>T CESC-US 10 35338621 35338621 single base substitution C G 3_prime_UTR_variant CESC-US 10 35338621 35338621 single base substitution C G missense_variant E109Q 325G>C CESC-US 10 35338621 35338621 single base substitution C G missense_variant E166Q 496G>C CESC-US 10 35338621 35338621 single base substitution C G missense_variant E185Q 553G>C CESC-US 10 35349897 35349897 single base substitution C T downstream_gene_variant CESC-US 10 35349897 35349897 single base substitution C T intron_variant CESC-US 10 35349897 35349897 single base substitution C T splice_acceptor_variant CESC-US 10 35368540 35368540 single base substitution G A intron_variant CLLE-ES 10 35295809 35295810 multiple base substitution (>=2bp and <=200bp) GC AA downstream_gene_variant CLLE-ES 10 35318303 35318303 single base substitution G A intron_variant CLLE-ES 10 35348396 35348396 single base substitution G A downstream_gene_variant CLLE-ES 10 35348396 35348396 single base substitution G A intron_variant COAD-US 10 35302705 35302705 single base substitution C T 3_prime_UTR_variant COAD-US 10 35302705 35302705 single base substitution C T synonymous_variant S580S 1740G>A COAD-US 10 35302705 35302705 single base substitution C T synonymous_variant S637S 1911G>A COAD-US 10 35302705 35302705 single base substitution C T synonymous_variant S656S 1968G>A COAD-US 10 35317808 35317808 single base substitution G A 3_prime_UTR_variant COAD-US 10 35317808 35317808 single base substitution G A missense_variant A459V 1376C>T COAD-US 10 35317808 35317808 single base substitution G A missense_variant A516V 1547C>T COAD-US 10 35317808 35317808 single base substitution G A missense_variant A535V 1604C>T COAD-US 10 35320266 35320266 single base substitution A C 3_prime_UTR_variant COAD-US 10 35320266 35320266 single base substitution A C missense_variant S393A 1177T>G COAD-US 10 35320266 35320266 single base substitution A C missense_variant S450A 1348T>G COAD-US 10 35320266 35320266 single base substitution A C missense_variant S469A 1405T>G COAD-US 10 35320266 35320266 single base substitution A G 3_prime_UTR_variant COAD-US 10 35320266 35320266 single base substitution A G missense_variant S393P 1177T>C COAD-US 10 35320266 35320266 single base substitution A G missense_variant S450P 1348T>C COAD-US 10 35320266 35320266 single base substitution A G missense_variant S469P 1405T>C COAD-US 10 35320289 35320289 single base substitution C T 3_prime_UTR_variant COAD-US 10 35320289 35320289 single base substitution C T missense_variant R385H 1154G>A COAD-US 10 35320289 35320289 single base substitution C T missense_variant R442H 1325G>A COAD-US 10 35320289 35320289 single base substitution C T missense_variant R461H 1382G>A COAD-US 10 35327980 35327980 single base substitution G A 3_prime_UTR_variant COAD-US 10 35327980 35327980 single base substitution G A stop_gained R192* 574C>T COAD-US 10 35327980 35327980 single base substitution G A stop_gained R249* 745C>T COAD-US 10 35327980 35327980 single base substitution G A stop_gained R268* 802C>T COCA-CN 10 35298301 35298301 single base substitution G A 3_prime_UTR_variant COCA-CN 10 35298301 35298301 single base substitution G A downstream_gene_variant COCA-CN 10 35299235 35299235 single base substitution G A 3_prime_UTR_variant COCA-CN 10 35300937 35300937 single base substitution T C intron_variant COCA-CN 10 35306803 35306803 single base substitution T A intron_variant COCA-CN 10 35311005 35311005 single base substitution G T intron_variant COCA-CN 10 35320326 35320326 single base substitution A C intron_variant COCA-CN 10 35320471 35320471 single base substitution G A 3_prime_UTR_variant COCA-CN 10 35320471 35320471 single base substitution G A missense_variant T359M 1076C>T COCA-CN 10 35320471 35320471 single base substitution G A missense_variant T416M 1247C>T COCA-CN 10 35320471 35320471 single base substitution G A missense_variant T435M 1304C>T COCA-CN 10 35328088 35328088 single base substitution A G intron_variant COCA-CN 10 35330478 35330478 single base substitution T C downstream_gene_variant COCA-CN 10 35330478 35330478 single base substitution T C intron_variant COCA-CN 10 35334985 35334985 single base substitution C T intron_variant COCA-CN 10 35338788 35338788 single base substitution G T intron_variant COCA-CN 10 35378078 35378078 single base substitution G C intron_variant COCA-CN 10 35378750 35378750 single base substitution A C intron_variant COCA-CN 10 35382582 35382582 single base substitution T C upstream_gene_variant ESAD-UK 10 35292575 35292575 single base substitution A T downstream_gene_variant ESAD-UK 10 35295142 35295142 single base substitution C A downstream_gene_variant ESAD-UK 10 35300216 35300216 single base substitution A T intron_variant ESAD-UK 10 35300335 35300335 single base substitution C T intron_variant ESAD-UK 10 35302705 35302705 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 35302705 35302705 single base substitution C T synonymous_variant S580S 1740G>A ESAD-UK 10 35302705 35302705 single base substitution C T synonymous_variant S637S 1911G>A ESAD-UK 10 35302705 35302705 single base substitution C T synonymous_variant S656S 1968G>A ESAD-UK 10 35308529 35308529 single base substitution T A intron_variant ESAD-UK 10 35311227 35311227 single base substitution C T intron_variant ESAD-UK 10 35311536 35311536 single base substitution T G intron_variant ESAD-UK 10 35312159 35312159 single base substitution A G intron_variant ESAD-UK 10 35312688 35312688 single base substitution A G intron_variant ESAD-UK 10 35321913 35321913 single base substitution C T intron_variant ESAD-UK 10 35322659 35322659 single base substitution C T intron_variant ESAD-UK 10 35326491 35326491 single base substitution G A intron_variant ESAD-UK 10 35328982 35328982 single base substitution G C downstream_gene_variant ESAD-UK 10 35328982 35328982 single base substitution G C intron_variant ESAD-UK 10 35330794 35330794 single base substitution T C downstream_gene_variant ESAD-UK 10 35330794 35330794 single base substitution T C intron_variant ESAD-UK 10 35334565 35334565 single base substitution C T intron_variant ESAD-UK 10 35335545 35335545 single base substitution C T intron_variant ESAD-UK 10 35335746 35335746 single base substitution G A intron_variant ESAD-UK 10 35336843 35336843 insertion of <=200bp - C intron_variant ESAD-UK 10 35340864 35340864 single base substitution G T intron_variant ESAD-UK 10 35341998 35341998 single base substitution G A intron_variant ESAD-UK 10 35342026 35342027 deletion of <=200bp TG - intron_variant ESAD-UK 10 35342794 35342794 single base substitution G A intron_variant ESAD-UK 10 35344394 35344394 single base substitution C T intron_variant ESAD-UK 10 35344709 35344709 single base substitution C T intron_variant ESAD-UK 10 35347482 35347482 single base substitution T C downstream_gene_variant ESAD-UK 10 35347482 35347482 single base substitution T C intron_variant ESAD-UK 10 35347569 35347569 single base substitution C A downstream_gene_variant ESAD-UK 10 35347569 35347569 single base substitution C A intron_variant ESAD-UK 10 35351038 35351038 single base substitution C T downstream_gene_variant ESAD-UK 10 35351038 35351038 single base substitution C T intron_variant ESAD-UK 10 35353644 35353644 single base substitution A T intron_variant ESAD-UK 10 35353825 35353825 single base substitution C T intron_variant ESAD-UK 10 35355288 35355288 single base substitution C G intron_variant ESAD-UK 10 35358606 35358606 single base substitution C A intron_variant ESAD-UK 10 35363912 35363912 single base substitution G A intron_variant ESAD-UK 10 35363912 35363912 single base substitution G A upstream_gene_variant ESAD-UK 10 35364383 35364383 single base substitution T C intron_variant ESAD-UK 10 35364383 35364383 single base substitution T C upstream_gene_variant ESAD-UK 10 35364634 35364634 single base substitution T C intron_variant ESAD-UK 10 35364634 35364634 single base substitution T C upstream_gene_variant ESAD-UK 10 35369976 35369976 single base substitution T A intron_variant ESAD-UK 10 35369977 35369977 single base substitution A T intron_variant ESAD-UK 10 35370374 35370374 single base substitution T A intron_variant ESAD-UK 10 35371586 35371586 single base substitution A G intron_variant ESAD-UK 10 35374063 35374063 insertion of <=200bp - TAC intron_variant ESAD-UK 10 35377299 35377299 single base substitution G A intron_variant ESAD-UK 10 35378052 35378052 single base substitution G A intron_variant ESAD-UK 10 35379014 35379014 insertion of <=200bp - GAGA intron_variant ESAD-UK 10 35379014 35379014 insertion of <=200bp - GAGA upstream_gene_variant ESAD-UK 10 35379015 35379020 deletion of <=200bp CCTCTC - intron_variant ESAD-UK 10 35379015 35379020 deletion of <=200bp CCTCTC - upstream_gene_variant ESAD-UK 10 35379273 35379273 single base substitution G A 5_prime_UTR_variant ESAD-UK 10 35379273 35379273 single base substitution G A intron_variant ESAD-UK 10 35379273 35379273 single base substitution G A upstream_gene_variant ESAD-UK 10 35380781 35380781 single base substitution C G upstream_gene_variant ESCA-CN 10 35314130 35314130 single base substitution T A splice_region_variant ESCA-CN 10 35327939 35327939 single base substitution C T 3_prime_UTR_variant ESCA-CN 10 35327939 35327939 single base substitution C T synonymous_variant V205V 615G>A ESCA-CN 10 35327939 35327939 single base substitution C T synonymous_variant V262V 786G>A ESCA-CN 10 35327939 35327939 single base substitution C T synonymous_variant V281V 843G>A GBM-US 10 35299303 35299303 single base substitution A T 3_prime_UTR_variant GBM-US 10 35299303 35299303 single base substitution A T missense_variant L668Q 2003T>A GBM-US 10 35299303 35299303 single base substitution A T missense_variant L686Q 2057T>A GBM-US 10 35299303 35299303 single base substitution A T missense_variant L725Q 2174T>A GBM-US 10 35299303 35299303 single base substitution A T missense_variant L744Q 2231T>A KIRC-US 10 35299283 35299283 single base substitution C T 3_prime_UTR_variant KIRC-US 10 35299283 35299283 single base substitution C T missense_variant E675K 2023G>A KIRC-US 10 35299283 35299283 single base substitution C T missense_variant E693K 2077G>A KIRC-US 10 35299283 35299283 single base substitution C T missense_variant E732K 2194G>A KIRC-US 10 35299283 35299283 single base substitution C T missense_variant E751K 2251G>A KIRP-US 10 35324145 35324145 single base substitution G T 3_prime_UTR_variant KIRP-US 10 35324145 35324145 single base substitution G T synonymous_variant I262I 786C>A KIRP-US 10 35324145 35324145 single base substitution G T synonymous_variant I319I 957C>A KIRP-US 10 35324145 35324145 single base substitution G T synonymous_variant I338I 1014C>A KIRP-US 10 35360197 35360197 single base substitution G C 5_prime_UTR_variant KIRP-US 10 35360197 35360197 single base substitution G C exon_variant KIRP-US 10 35360197 35360197 single base substitution G C missense_variant L17V 49C>G KIRP-US 10 35360197 35360197 single base substitution G C missense_variant L36V 106C>G LAML-KR 10 35321515 35321515 single base substitution A C intron_variant LAML-KR 10 35321519 35321519 single base substitution C A intron_variant LAML-KR 10 35322024 35322024 single base substitution G A intron_variant LICA-CN 10 35305133 35305133 single base substitution T A 3_prime_UTR_variant LICA-CN 10 35305133 35305133 single base substitution T A missense_variant H568L 1703A>T LICA-CN 10 35305133 35305133 single base substitution T A missense_variant H625L 1874A>T LICA-CN 10 35305133 35305133 single base substitution T A missense_variant H644L 1931A>T LICA-CN 10 35314093 35314093 single base substitution T G 3_prime_UTR_variant LICA-CN 10 35314093 35314093 single base substitution T G synonymous_variant R494R 1480A>C LICA-CN 10 35314093 35314093 single base substitution T G synonymous_variant R551R 1651A>C LICA-CN 10 35314093 35314093 single base substitution T G synonymous_variant R570R 1708A>C LICA-CN 10 35317751 35317751 single base substitution T C 3_prime_UTR_variant LICA-CN 10 35317751 35317751 single base substitution T C missense_variant K478R 1433A>G LICA-CN 10 35317751 35317751 single base substitution T C missense_variant K535R 1604A>G LICA-CN 10 35317751 35317751 single base substitution T C missense_variant K554R 1661A>G LICA-FR 10 35324141 35324141 single base substitution C G 3_prime_UTR_variant LICA-FR 10 35324141 35324141 single base substitution C G missense_variant D264H 790G>C LICA-FR 10 35324141 35324141 single base substitution C G missense_variant D321H 961G>C LICA-FR 10 35324141 35324141 single base substitution C G missense_variant D340H 1018G>C LICA-FR 10 35325924 35325924 single base substitution T A intron_variant LICA-FR 10 35355282 35355282 single base substitution C T intron_variant LICA-FR 10 35360147 35360147 single base substitution T C 5_prime_UTR_variant LICA-FR 10 35360147 35360147 single base substitution T C exon_variant LICA-FR 10 35360147 35360147 single base substitution T C synonymous_variant A33A 99A>G LICA-FR 10 35360147 35360147 single base substitution T C synonymous_variant A52A 156A>G LICA-FR 10 35364564 35364564 insertion of <=200bp - AC intron_variant LICA-FR 10 35364564 35364564 insertion of <=200bp - AC upstream_gene_variant LICA-FR 10 35369478 35369478 single base substitution T A intron_variant LIHC-US 10 35333758 35333758 single base substitution T C 3_prime_UTR_variant LIHC-US 10 35333758 35333758 single base substitution T C missense_variant H125R 374A>G LIHC-US 10 35333758 35333758 single base substitution T C missense_variant H182R 545A>G LIHC-US 10 35333758 35333758 single base substitution T C missense_variant H201R 602A>G LINC-JP 10 35298048 35298048 single base substitution G T 3_prime_UTR_variant LINC-JP 10 35298048 35298048 single base substitution G T downstream_gene_variant LINC-JP 10 35300146 35300146 single base substitution T A intron_variant LINC-JP 10 35305233 35305233 single base substitution C T 3_prime_UTR_variant LINC-JP 10 35305233 35305233 single base substitution C T missense_variant E535K 1603G>A LINC-JP 10 35305233 35305233 single base substitution C T missense_variant E592K 1774G>A LINC-JP 10 35305233 35305233 single base substitution C T missense_variant E611K 1831G>A LINC-JP 10 35310079 35310079 single base substitution C A intron_variant LINC-JP 10 35310335 35310335 single base substitution A G intron_variant LINC-JP 10 35310384 35310384 single base substitution T C intron_variant LINC-JP 10 35310388 35310388 single base substitution T C intron_variant LINC-JP 10 35310465 35310465 single base substitution A C intron_variant LINC-JP 10 35310474 35310474 single base substitution T G intron_variant LINC-JP 10 35310532 35310532 single base substitution T C intron_variant LINC-JP 10 35310542 35310542 single base substitution T A intron_variant LINC-JP 10 35310682 35310682 single base substitution T C intron_variant LINC-JP 10 35310690 35310690 single base substitution G C intron_variant LINC-JP 10 35310702 35310702 single base substitution C T intron_variant LINC-JP 10 35312400 35312400 single base substitution C T intron_variant LINC-JP 10 35314147 35314147 single base substitution C A intron_variant LINC-JP 10 35321189 35321189 single base substitution G T intron_variant LINC-JP 10 35321657 35321657 single base substitution C T intron_variant LINC-JP 10 35324322 35324322 single base substitution G A intron_variant LINC-JP 10 35335070 35335070 single base substitution G T intron_variant LINC-JP 10 35338420 35338420 single base substitution A G intron_variant LINC-JP 10 35342649 35342649 single base substitution A G intron_variant LINC-JP 10 35344467 35344467 single base substitution C T intron_variant LINC-JP 10 35348779 35348779 single base substitution C G downstream_gene_variant LINC-JP 10 35348779 35348779 single base substitution C G intron_variant LINC-JP 10 35350896 35350896 single base substitution T C downstream_gene_variant LINC-JP 10 35350896 35350896 single base substitution T C intron_variant LINC-JP 10 35367578 35367578 single base substitution G C intron_variant LINC-JP 10 35367578 35367578 single base substitution G C upstream_gene_variant LINC-JP 10 35368595 35368595 single base substitution T C intron_variant LINC-JP 10 35371303 35371303 single base substitution G A intron_variant LINC-JP 10 35378330 35378330 single base substitution T C intron_variant LINC-JP 10 35382653 35382653 single base substitution T C upstream_gene_variant LIRI-JP 10 35295081 35295081 single base substitution A C downstream_gene_variant LIRI-JP 10 35295812 35295812 single base substitution C T downstream_gene_variant LIRI-JP 10 35297424 35297424 single base substitution A G downstream_gene_variant LIRI-JP 10 35298436 35298436 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 35298436 35298436 single base substitution T C downstream_gene_variant LIRI-JP 10 35298838 35298838 deletion of <=200bp T - 3_prime_UTR_variant LIRI-JP 10 35298838 35298838 deletion of <=200bp T - downstream_gene_variant LIRI-JP 10 35299513 35299513 single base substitution T C intron_variant LIRI-JP 10 35299715 35299715 single base substitution G A intron_variant LIRI-JP 10 35300064 35300064 single base substitution T A intron_variant LIRI-JP 10 35303500 35303500 single base substitution T C intron_variant LIRI-JP 10 35305503 35305503 single base substitution T C intron_variant LIRI-JP 10 35308405 35308405 single base substitution C T intron_variant LIRI-JP 10 35308804 35308804 single base substitution A C intron_variant LIRI-JP 10 35309634 35309634 single base substitution A T intron_variant LIRI-JP 10 35309744 35309744 single base substitution T C intron_variant LIRI-JP 10 35311408 35311408 single base substitution C G intron_variant LIRI-JP 10 35311669 35311669 single base substitution T G intron_variant LIRI-JP 10 35312159 35312159 single base substitution A C intron_variant LIRI-JP 10 35312322 35312322 single base substitution T C intron_variant LIRI-JP 10 35313025 35313025 single base substitution A T intron_variant LIRI-JP 10 35314009 35314009 single base substitution A G intron_variant LIRI-JP 10 35316915 35316915 single base substitution C A intron_variant LIRI-JP 10 35318453 35318453 single base substitution A G 3_prime_UTR_variant LIRI-JP 10 35318453 35318453 single base substitution A G missense_variant I444T 1331T>C LIRI-JP 10 35318453 35318453 single base substitution A G missense_variant I501T 1502T>C LIRI-JP 10 35318453 35318453 single base substitution A G missense_variant I520T 1559T>C LIRI-JP 10 35318501 35318513 deletion of <=200bp TCAGCGCTGACAC - 3_prime_UTR_variant LIRI-JP 10 35318501 35318513 deletion of <=200bp TCAGCGCTGACAC - frameshift_variant SVSAD424 LIRI-JP 10 35318501 35318513 deletion of <=200bp TCAGCGCTGACAC - frameshift_variant SVSAD481 LIRI-JP 10 35318501 35318513 deletion of <=200bp TCAGCGCTGACAC - frameshift_variant SVSAD500 LIRI-JP 10 35321491 35321491 single base substitution C T intron_variant LIRI-JP 10 35322058 35322058 single base substitution A T intron_variant LIRI-JP 10 35322318 35322318 single base substitution G T intron_variant LIRI-JP 10 35322570 35322570 single base substitution C T intron_variant LIRI-JP 10 35323675 35323675 single base substitution T C intron_variant LIRI-JP 10 35323788 35323788 single base substitution C T intron_variant LIRI-JP 10 35325539 35325539 single base substitution T C intron_variant LIRI-JP 10 35325947 35325947 single base substitution T C intron_variant LIRI-JP 10 35328872 35328872 single base substitution G A downstream_gene_variant LIRI-JP 10 35328872 35328872 single base substitution G A intron_variant LIRI-JP 10 35330262 35330262 single base substitution G T downstream_gene_variant LIRI-JP 10 35330262 35330262 single base substitution G T intron_variant LIRI-JP 10 35330669 35330669 single base substitution T A downstream_gene_variant LIRI-JP 10 35330669 35330669 single base substitution T A intron_variant LIRI-JP 10 35332057 35332057 single base substitution T C downstream_gene_variant LIRI-JP 10 35332057 35332057 single base substitution T C intron_variant LIRI-JP 10 35332208 35332208 insertion of <=200bp - G downstream_gene_variant LIRI-JP 10 35332208 35332208 insertion of <=200bp - G intron_variant LIRI-JP 10 35332364 35332364 single base substitution A C downstream_gene_variant LIRI-JP 10 35332364 35332364 single base substitution A C intron_variant LIRI-JP 10 35334249 35334249 single base substitution G A intron_variant LIRI-JP 10 35337256 35337256 single base substitution T C intron_variant LIRI-JP 10 35339301 35339301 single base substitution T C intron_variant LIRI-JP 10 35341343 35341353 deletion of <=200bp ACCCAGTCTAT - intron_variant LIRI-JP 10 35343228 35343231 deletion of <=200bp TTTA - intron_variant LIRI-JP 10 35343500 35343500 single base substitution A C intron_variant LIRI-JP 10 35343575 35343575 single base substitution T C intron_variant LIRI-JP 10 35344506 35344506 single base substitution T C intron_variant LIRI-JP 10 35349438 35349438 single base substitution T C downstream_gene_variant LIRI-JP 10 35349438 35349438 single base substitution T C intron_variant LIRI-JP 10 35353969 35353969 single base substitution T C intron_variant LIRI-JP 10 35354088 35354088 single base substitution A G intron_variant LIRI-JP 10 35354470 35354470 single base substitution C T intron_variant LIRI-JP 10 35356534 35356534 single base substitution C T intron_variant LIRI-JP 10 35357124 35357124 single base substitution T C intron_variant LIRI-JP 10 35357396 35357396 single base substitution T C intron_variant LIRI-JP 10 35357917 35357917 single base substitution C T intron_variant LIRI-JP 10 35358315 35358315 single base substitution A G intron_variant LIRI-JP 10 35359591 35359591 single base substitution T A intron_variant LIRI-JP 10 35359860 35359860 single base substitution A T intron_variant LIRI-JP 10 35359904 35359904 single base substitution A G intron_variant LIRI-JP 10 35361086 35361086 single base substitution T A intron_variant LIRI-JP 10 35361086 35361086 single base substitution T A upstream_gene_variant LIRI-JP 10 35361208 35361208 single base substitution C A intron_variant LIRI-JP 10 35361208 35361208 single base substitution C A upstream_gene_variant LIRI-JP 10 35363023 35363023 single base substitution T C intron_variant LIRI-JP 10 35363023 35363023 single base substitution T C upstream_gene_variant LIRI-JP 10 35365049 35365049 single base substitution T C intron_variant LIRI-JP 10 35365049 35365049 single base substitution T C upstream_gene_variant LIRI-JP 10 35369510 35369510 single base substitution T A intron_variant LIRI-JP 10 35373640 35373640 single base substitution A G intron_variant LIRI-JP 10 35374593 35374593 single base substitution C T intron_variant LIRI-JP 10 35378210 35378210 single base substitution G C intron_variant LIRI-JP 10 35378425 35378425 single base substitution C A intron_variant LIRI-JP 10 35380454 35380454 single base substitution C A upstream_gene_variant LIRI-JP 10 35382783 35382783 single base substitution T C upstream_gene_variant LIRI-JP 10 35383255 35383255 single base substitution C T upstream_gene_variant LIRI-JP 10 35383679 35383679 single base substitution G T upstream_gene_variant LUSC-KR 10 35293473 35293473 single base substitution T C downstream_gene_variant LUSC-KR 10 35300623 35300623 single base substitution G A intron_variant LUSC-KR 10 35303796 35303796 single base substitution A G intron_variant LUSC-KR 10 35321515 35321515 single base substitution A C intron_variant LUSC-KR 10 35327261 35327261 single base substitution G C intron_variant LUSC-KR 10 35327947 35327947 single base substitution T C 3_prime_UTR_variant LUSC-KR 10 35327947 35327947 single base substitution T C missense_variant T203A 607A>G LUSC-KR 10 35327947 35327947 single base substitution T C missense_variant T260A 778A>G LUSC-KR 10 35327947 35327947 single base substitution T C missense_variant T279A 835A>G LUSC-KR 10 35331722 35331722 single base substitution C A downstream_gene_variant LUSC-KR 10 35331722 35331722 single base substitution C A intron_variant LUSC-KR 10 35337608 35337608 single base substitution C T intron_variant LUSC-KR 10 35338143 35338143 single base substitution C A intron_variant LUSC-KR 10 35338144 35338144 single base substitution C T intron_variant LUSC-KR 10 35341822 35341822 single base substitution C A intron_variant LUSC-KR 10 35342845 35342845 single base substitution G A intron_variant LUSC-KR 10 35345233 35345233 single base substitution C A downstream_gene_variant LUSC-KR 10 35345233 35345233 single base substitution C A intron_variant LUSC-KR 10 35350716 35350716 single base substitution G T downstream_gene_variant LUSC-KR 10 35350716 35350716 single base substitution G T intron_variant LUSC-KR 10 35351721 35351721 single base substitution C T downstream_gene_variant LUSC-KR 10 35351721 35351721 single base substitution C T intron_variant LUSC-KR 10 35353045 35353045 single base substitution C T intron_variant LUSC-KR 10 35353045 35353045 single base substitution C T splice_acceptor_variant LUSC-KR 10 35357375 35357375 single base substitution C T intron_variant LUSC-KR 10 35362095 35362095 single base substitution C G intron_variant LUSC-KR 10 35362095 35362095 single base substitution C G upstream_gene_variant LUSC-KR 10 35362155 35362155 single base substitution T C intron_variant LUSC-KR 10 35362155 35362155 single base substitution T C upstream_gene_variant LUSC-KR 10 35371294 35371294 single base substitution G T intron_variant LUSC-KR 10 35371370 35371370 single base substitution T C intron_variant LUSC-KR 10 35372216 35372216 single base substitution C T intron_variant LUSC-KR 10 35373331 35373331 single base substitution G A intron_variant LUSC-KR 10 35374651 35374651 single base substitution T A intron_variant LUSC-KR 10 35375163 35375163 single base substitution G A intron_variant LUSC-KR 10 35376598 35376598 single base substitution C A intron_variant LUSC-KR 10 35382265 35382265 single base substitution A T upstream_gene_variant LUSC-KR 10 35382303 35382303 single base substitution G C upstream_gene_variant LUSC-KR 10 35384240 35384240 single base substitution G T upstream_gene_variant LUSC-US 10 35324157 35324157 single base substitution C T 3_prime_UTR_variant LUSC-US 10 35324157 35324157 single base substitution C T synonymous_variant L258L 774G>A LUSC-US 10 35324157 35324157 single base substitution C T synonymous_variant L315L 945G>A LUSC-US 10 35324157 35324157 single base substitution C T synonymous_variant L334L 1002G>A LUSC-US 10 35333790 35333790 single base substitution A C 3_prime_UTR_variant LUSC-US 10 35333790 35333790 single base substitution A C synonymous_variant R114R 342T>G LUSC-US 10 35333790 35333790 single base substitution A C synonymous_variant R171R 513T>G LUSC-US 10 35333790 35333790 single base substitution A C synonymous_variant R190R 570T>G MALY-DE 10 35293226 35293226 single base substitution G A downstream_gene_variant MALY-DE 10 35302910 35302910 single base substitution A C intron_variant MALY-DE 10 35311946 35311946 single base substitution G C intron_variant MALY-DE 10 35333450 35333450 single base substitution A T downstream_gene_variant MALY-DE 10 35333450 35333450 single base substitution A T intron_variant MALY-DE 10 35335059 35335059 single base substitution G A intron_variant MALY-DE 10 35337846 35337846 single base substitution A T intron_variant MALY-DE 10 35342026 35342027 deletion of <=200bp TG - intron_variant MALY-DE 10 35355333 35355333 single base substitution T G intron_variant MALY-DE 10 35361545 35361545 single base substitution C T intron_variant MALY-DE 10 35361545 35361545 single base substitution C T upstream_gene_variant MALY-DE 10 35363733 35363733 single base substitution A G intron_variant MALY-DE 10 35363733 35363733 single base substitution A G upstream_gene_variant MALY-DE 10 35365290 35365290 single base substitution A C intron_variant MALY-DE 10 35365290 35365290 single base substitution A C upstream_gene_variant MALY-DE 10 35365297 35365297 single base substitution A C intron_variant MALY-DE 10 35365297 35365297 single base substitution A C upstream_gene_variant MALY-DE 10 35368532 35368532 single base substitution A C intron_variant MALY-DE 10 35369673 35369673 single base substitution G A intron_variant MALY-DE 10 35370376 35370376 single base substitution A T intron_variant MALY-DE 10 35381720 35381720 single base substitution T A upstream_gene_variant MALY-DE 10 35383730 35383730 single base substitution A G upstream_gene_variant MALY-DE 10 35384493 35384493 single base substitution A G upstream_gene_variant MELA-AU 10 35293275 35293275 single base substitution G A downstream_gene_variant MELA-AU 10 35293347 35293347 single base substitution G A downstream_gene_variant MELA-AU 10 35294366 35294366 single base substitution C T downstream_gene_variant MELA-AU 10 35294426 35294426 single base substitution G A downstream_gene_variant MELA-AU 10 35294910 35294910 single base substitution G A downstream_gene_variant MELA-AU 10 35295169 35295169 single base substitution G A downstream_gene_variant MELA-AU 10 35295198 35295198 single base substitution G A downstream_gene_variant MELA-AU 10 35295299 35295299 single base substitution G A downstream_gene_variant MELA-AU 10 35296561 35296561 single base substitution G A downstream_gene_variant MELA-AU 10 35296662 35296662 single base substitution G A downstream_gene_variant MELA-AU 10 35298008 35298008 single base substitution A T 3_prime_UTR_variant MELA-AU 10 35298008 35298008 single base substitution A T downstream_gene_variant MELA-AU 10 35299032 35299032 single base substitution T C 3_prime_UTR_variant MELA-AU 10 35299032 35299032 single base substitution T C downstream_gene_variant MELA-AU 10 35299387 35299387 single base substitution G A intron_variant MELA-AU 10 35300343 35300343 single base substitution C T intron_variant MELA-AU 10 35300529 35300529 single base substitution G A intron_variant MELA-AU 10 35300754 35300754 single base substitution C T intron_variant MELA-AU 10 35300826 35300826 single base substitution G C 3_prime_UTR_variant MELA-AU 10 35300826 35300826 single base substitution G C intron_variant MELA-AU 10 35300826 35300826 single base substitution G C missense_variant R629G 1885C>G MELA-AU 10 35300826 35300826 single base substitution G C missense_variant R686G 2056C>G MELA-AU 10 35300826 35300826 single base substitution G C missense_variant R705G 2113C>G MELA-AU 10 35300911 35300911 single base substitution G A intron_variant MELA-AU 10 35300953 35300953 single base substitution C G intron_variant MELA-AU 10 35301120 35301120 single base substitution T A intron_variant MELA-AU 10 35301548 35301548 single base substitution G A intron_variant MELA-AU 10 35301927 35301927 single base substitution A T intron_variant MELA-AU 10 35302188 35302188 single base substitution G A intron_variant MELA-AU 10 35302837 35302837 single base substitution C T intron_variant MELA-AU 10 35302904 35302904 single base substitution G A intron_variant MELA-AU 10 35303521 35303521 single base substitution G A intron_variant MELA-AU 10 35303590 35303590 single base substitution G T intron_variant MELA-AU 10 35305365 35305365 single base substitution G A intron_variant MELA-AU 10 35305555 35305555 single base substitution G A intron_variant MELA-AU 10 35305838 35305838 single base substitution G A intron_variant MELA-AU 10 35306062 35306062 single base substitution G A intron_variant MELA-AU 10 35306195 35306195 single base substitution G A intron_variant MELA-AU 10 35307027 35307027 single base substitution A T intron_variant MELA-AU 10 35307109 35307109 single base substitution G A intron_variant MELA-AU 10 35307225 35307225 single base substitution A C intron_variant MELA-AU 10 35307230 35307230 single base substitution A C intron_variant MELA-AU 10 35307892 35307892 single base substitution G A intron_variant MELA-AU 10 35308355 35308355 single base substitution T A intron_variant MELA-AU 10 35308894 35308894 single base substitution G A intron_variant MELA-AU 10 35309078 35309078 single base substitution G A intron_variant MELA-AU 10 35309283 35309283 single base substitution G A intron_variant MELA-AU 10 35309714 35309714 single base substitution G A intron_variant MELA-AU 10 35309889 35309889 single base substitution G A intron_variant MELA-AU 10 35310209 35310209 single base substitution G A intron_variant MELA-AU 10 35310923 35310923 single base substitution G A intron_variant MELA-AU 10 35311556 35311556 single base substitution G A intron_variant MELA-AU 10 35312091 35312091 single base substitution C T intron_variant MELA-AU 10 35312266 35312266 single base substitution C T intron_variant MELA-AU 10 35312758 35312758 single base substitution T C intron_variant MELA-AU 10 35312780 35312780 single base substitution T C intron_variant MELA-AU 10 35313273 35313273 single base substitution G A intron_variant MELA-AU 10 35313594 35313594 single base substitution G A intron_variant MELA-AU 10 35313836 35313836 single base substitution A T intron_variant MELA-AU 10 35314347 35314347 single base substitution T C intron_variant MELA-AU 10 35314565 35314565 single base substitution G A intron_variant MELA-AU 10 35315249 35315249 single base substitution G A intron_variant MELA-AU 10 35315358 35315358 single base substitution G A intron_variant MELA-AU 10 35315390 35315390 single base substitution C T intron_variant MELA-AU 10 35317400 35317400 single base substitution G A intron_variant MELA-AU 10 35317823 35317823 single base substitution G A splice_region_variant MELA-AU 10 35318172 35318172 single base substitution G A intron_variant MELA-AU 10 35318381 35318410 deletion of <=200bp TTAGTAAATGCTCATAGTAAAACACATATT - splice_region_variant MELA-AU 10 35318925 35318925 single base substitution G A intron_variant MELA-AU 10 35320281 35320281 single base substitution G A 3_prime_UTR_variant MELA-AU 10 35320281 35320281 single base substitution G A missense_variant H388Y 1162C>T MELA-AU 10 35320281 35320281 single base substitution G A missense_variant H445Y 1333C>T MELA-AU 10 35320281 35320281 single base substitution G A missense_variant H464Y 1390C>T MELA-AU 10 35320395 35320395 single base substitution G A intron_variant MELA-AU 10 35320676 35320676 single base substitution G A intron_variant MELA-AU 10 35321241 35321241 single base substitution G A intron_variant MELA-AU 10 35321658 35321658 single base substitution G A intron_variant MELA-AU 10 35322470 35322470 single base substitution C T intron_variant MELA-AU 10 35324624 35324624 single base substitution G A intron_variant MELA-AU 10 35325114 35325114 single base substitution G T intron_variant MELA-AU 10 35325371 35325371 single base substitution G A intron_variant MELA-AU 10 35325824 35325824 single base substitution G A intron_variant MELA-AU 10 35327216 35327216 single base substitution G A intron_variant MELA-AU 10 35327601 35327601 single base substitution G A intron_variant MELA-AU 10 35327769 35327769 single base substitution A G intron_variant MELA-AU 10 35327866 35327866 single base substitution G A 3_prime_UTR_variant MELA-AU 10 35327866 35327866 single base substitution G A stop_gained R230* 688C>T MELA-AU 10 35327866 35327866 single base substitution G A stop_gained R287* 859C>T MELA-AU 10 35327866 35327866 single base substitution G A stop_gained R306* 916C>T MELA-AU 10 35328571 35328571 single base substitution T A downstream_gene_variant MELA-AU 10 35328571 35328571 single base substitution T A intron_variant MELA-AU 10 35328873 35328873 single base substitution G A downstream_gene_variant MELA-AU 10 35328873 35328873 single base substitution G A intron_variant MELA-AU 10 35329008 35329008 single base substitution G A downstream_gene_variant MELA-AU 10 35329008 35329008 single base substitution G A intron_variant MELA-AU 10 35329238 35329238 single base substitution G A downstream_gene_variant MELA-AU 10 35329238 35329238 single base substitution G A intron_variant MELA-AU 10 35330866 35330866 single base substitution A T downstream_gene_variant MELA-AU 10 35330866 35330866 single base substitution A T intron_variant MELA-AU 10 35331508 35331508 single base substitution G A downstream_gene_variant MELA-AU 10 35331508 35331508 single base substitution G A intron_variant MELA-AU 10 35331749 35331749 single base substitution G A downstream_gene_variant MELA-AU 10 35331749 35331749 single base substitution G A intron_variant MELA-AU 10 35333292 35333292 single base substitution A G downstream_gene_variant MELA-AU 10 35333292 35333292 single base substitution A G intron_variant MELA-AU 10 35333639 35333639 single base substitution T C intron_variant MELA-AU 10 35333742 35333742 single base substitution G A 3_prime_UTR_variant MELA-AU 10 35333742 35333742 single base substitution G A synonymous_variant S130S 390C>T MELA-AU 10 35333742 35333742 single base substitution G A synonymous_variant S187S 561C>T MELA-AU 10 35333742 35333742 single base substitution G A synonymous_variant S206S 618C>T MELA-AU 10 35333884 35333884 single base substitution T C intron_variant MELA-AU 10 35336975 35336975 single base substitution G A intron_variant MELA-AU 10 35337032 35337032 single base substitution G A intron_variant MELA-AU 10 35337042 35337042 single base substitution G A intron_variant MELA-AU 10 35337581 35337581 single base substitution G A intron_variant MELA-AU 10 35337643 35337643 single base substitution G A intron_variant MELA-AU 10 35339266 35339266 single base substitution A G intron_variant MELA-AU 10 35339569 35339569 single base substitution G A intron_variant MELA-AU 10 35339888 35339889 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 35340170 35340170 single base substitution G A intron_variant MELA-AU 10 35340270 35340271 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 35340438 35340438 single base substitution G A intron_variant MELA-AU 10 35340880 35340880 single base substitution C T intron_variant MELA-AU 10 35341069 35341069 single base substitution C T intron_variant MELA-AU 10 35341337 35341337 single base substitution C T intron_variant MELA-AU 10 35341454 35341454 single base substitution A C intron_variant MELA-AU 10 35343172 35343172 single base substitution G A intron_variant MELA-AU 10 35343673 35343673 single base substitution A C intron_variant MELA-AU 10 35344043 35344043 single base substitution A G intron_variant MELA-AU 10 35344437 35344437 single base substitution G A intron_variant MELA-AU 10 35344490 35344490 single base substitution C T intron_variant MELA-AU 10 35344686 35344686 single base substitution A G intron_variant MELA-AU 10 35344769 35344769 single base substitution G A intron_variant MELA-AU 10 35345532 35345532 single base substitution G A downstream_gene_variant MELA-AU 10 35345532 35345532 single base substitution G A intron_variant MELA-AU 10 35347001 35347001 single base substitution G A downstream_gene_variant MELA-AU 10 35347001 35347001 single base substitution G A intron_variant MELA-AU 10 35347003 35347003 single base substitution G A downstream_gene_variant MELA-AU 10 35347003 35347003 single base substitution G A intron_variant MELA-AU 10 35347427 35347427 single base substitution T C downstream_gene_variant MELA-AU 10 35347427 35347427 single base substitution T C intron_variant MELA-AU 10 35347726 35347726 single base substitution G A downstream_gene_variant MELA-AU 10 35347726 35347726 single base substitution G A intron_variant MELA-AU 10 35348112 35348112 single base substitution T C downstream_gene_variant MELA-AU 10 35348112 35348112 single base substitution T C intron_variant MELA-AU 10 35348349 35348349 single base substitution G A downstream_gene_variant MELA-AU 10 35348349 35348349 single base substitution G A intron_variant MELA-AU 10 35348688 35348688 single base substitution G A downstream_gene_variant MELA-AU 10 35348688 35348688 single base substitution G A intron_variant MELA-AU 10 35350177 35350177 single base substitution G A downstream_gene_variant MELA-AU 10 35350177 35350177 single base substitution G A intron_variant MELA-AU 10 35351376 35351376 single base substitution C T downstream_gene_variant MELA-AU 10 35351376 35351376 single base substitution C T intron_variant MELA-AU 10 35351673 35351673 single base substitution G A downstream_gene_variant MELA-AU 10 35351673 35351673 single base substitution G A intron_variant MELA-AU 10 35351675 35351675 single base substitution G A downstream_gene_variant MELA-AU 10 35351675 35351675 single base substitution G A intron_variant MELA-AU 10 35351700 35351700 single base substitution G A downstream_gene_variant MELA-AU 10 35351700 35351700 single base substitution G A intron_variant MELA-AU 10 35351958 35351958 single base substitution T C downstream_gene_variant MELA-AU 10 35351958 35351958 single base substitution T C exon_variant MELA-AU 10 35351958 35351958 single base substitution T C missense_variant E51G 152A>G MELA-AU 10 35351958 35351958 single base substitution T C missense_variant E70G 209A>G MELA-AU 10 35351958 35351958 single base substitution T C missense_variant N9D 25A>G MELA-AU 10 35352229 35352229 single base substitution G A downstream_gene_variant MELA-AU 10 35352229 35352229 single base substitution G A intron_variant MELA-AU 10 35352885 35352885 single base substitution G A exon_variant MELA-AU 10 35352885 35352885 single base substitution G A intron_variant MELA-AU 10 35353256 35353256 single base substitution G A intron_variant MELA-AU 10 35353867 35353867 single base substitution G A intron_variant MELA-AU 10 35354070 35354070 single base substitution A G intron_variant MELA-AU 10 35354876 35354876 single base substitution G A intron_variant MELA-AU 10 35355528 35355528 single base substitution G A intron_variant MELA-AU 10 35355901 35355901 single base substitution G A intron_variant MELA-AU 10 35356266 35356266 single base substitution G A intron_variant MELA-AU 10 35356828 35356828 single base substitution G T intron_variant MELA-AU 10 35357986 35357986 single base substitution G A intron_variant MELA-AU 10 35358242 35358242 single base substitution G A intron_variant MELA-AU 10 35358672 35358672 single base substitution C T intron_variant MELA-AU 10 35359332 35359332 single base substitution A G intron_variant MELA-AU 10 35359484 35359484 single base substitution T C intron_variant MELA-AU 10 35360356 35360357 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 35360356 35360357 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 35360785 35360785 single base substitution G A intron_variant MELA-AU 10 35360785 35360785 single base substitution G A upstream_gene_variant MELA-AU 10 35360797 35360798 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 35360797 35360798 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 35361488 35361488 single base substitution G A intron_variant MELA-AU 10 35361488 35361488 single base substitution G A upstream_gene_variant MELA-AU 10 35361828 35361828 single base substitution G A intron_variant MELA-AU 10 35361828 35361828 single base substitution G A upstream_gene_variant MELA-AU 10 35362024 35362024 single base substitution G A intron_variant MELA-AU 10 35362024 35362024 single base substitution G A upstream_gene_variant MELA-AU 10 35362160 35362160 single base substitution G A intron_variant MELA-AU 10 35362160 35362160 single base substitution G A upstream_gene_variant MELA-AU 10 35362693 35362693 single base substitution C T intron_variant MELA-AU 10 35362693 35362693 single base substitution C T upstream_gene_variant MELA-AU 10 35364082 35364082 single base substitution G A intron_variant MELA-AU 10 35364082 35364082 single base substitution G A upstream_gene_variant MELA-AU 10 35364968 35364968 single base substitution G A intron_variant MELA-AU 10 35364968 35364968 single base substitution G A upstream_gene_variant MELA-AU 10 35365392 35365392 single base substitution A T intron_variant MELA-AU 10 35365392 35365392 single base substitution A T upstream_gene_variant MELA-AU 10 35365907 35365907 single base substitution G A intron_variant MELA-AU 10 35365907 35365907 single base substitution G A upstream_gene_variant MELA-AU 10 35367358 35367358 single base substitution G A intron_variant MELA-AU 10 35367358 35367358 single base substitution G A upstream_gene_variant MELA-AU 10 35367419 35367419 single base substitution G A intron_variant MELA-AU 10 35367419 35367419 single base substitution G A upstream_gene_variant MELA-AU 10 35368000 35368000 single base substitution G A intron_variant MELA-AU 10 35368000 35368000 single base substitution G A upstream_gene_variant MELA-AU 10 35369820 35369820 single base substitution G A intron_variant MELA-AU 10 35370295 35370295 single base substitution G A intron_variant MELA-AU 10 35370405 35370405 single base substitution G A intron_variant MELA-AU 10 35370503 35370503 single base substitution T C intron_variant MELA-AU 10 35371016 35371016 single base substitution G A intron_variant MELA-AU 10 35371128 35371128 single base substitution G A intron_variant MELA-AU 10 35371229 35371229 single base substitution G A intron_variant MELA-AU 10 35371231 35371231 single base substitution A C intron_variant MELA-AU 10 35371327 35371327 single base substitution G A intron_variant MELA-AU 10 35371560 35371560 single base substitution C G intron_variant MELA-AU 10 35372327 35372327 single base substitution C T intron_variant MELA-AU 10 35372634 35372634 single base substitution T C intron_variant MELA-AU 10 35374037 35374037 single base substitution G A intron_variant MELA-AU 10 35374273 35374273 single base substitution G A intron_variant MELA-AU 10 35374345 35374345 single base substitution G A intron_variant MELA-AU 10 35374772 35374772 single base substitution G A intron_variant MELA-AU 10 35375275 35375275 single base substitution G A intron_variant MELA-AU 10 35375644 35375644 single base substitution C T intron_variant MELA-AU 10 35375952 35375952 single base substitution G A intron_variant MELA-AU 10 35375980 35375980 single base substitution A G intron_variant MELA-AU 10 35376463 35376465 deletion of <=200bp AAC - intron_variant MELA-AU 10 35377232 35377232 single base substitution T C intron_variant MELA-AU 10 35379529 35379529 single base substitution C T 5_prime_UTR_variant MELA-AU 10 35379529 35379529 single base substitution C T upstream_gene_variant MELA-AU 10 35379562 35379562 single base substitution G A 5_prime_UTR_variant MELA-AU 10 35379562 35379562 single base substitution G A upstream_gene_variant MELA-AU 10 35379611 35379611 single base substitution C T upstream_gene_variant MELA-AU 10 35380224 35380225 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 35380629 35380629 single base substitution A G upstream_gene_variant MELA-AU 10 35381005 35381005 single base substitution G A upstream_gene_variant MELA-AU 10 35381141 35381141 single base substitution C T upstream_gene_variant MELA-AU 10 35381303 35381303 single base substitution C T upstream_gene_variant MELA-AU 10 35381552 35381552 single base substitution C T upstream_gene_variant MELA-AU 10 35381702 35381702 single base substitution C A upstream_gene_variant MELA-AU 10 35381848 35381848 single base substitution G A upstream_gene_variant MELA-AU 10 35382172 35382172 single base substitution C T upstream_gene_variant MELA-AU 10 35382192 35382192 single base substitution C T upstream_gene_variant MELA-AU 10 35382334 35382334 single base substitution C T upstream_gene_variant MELA-AU 10 35382379 35382379 single base substitution G A upstream_gene_variant MELA-AU 10 35382931 35382931 single base substitution C T upstream_gene_variant MELA-AU 10 35383193 35383193 single base substitution C T upstream_gene_variant MELA-AU 10 35383205 35383205 single base substitution C T upstream_gene_variant MELA-AU 10 35383318 35383318 single base substitution C T upstream_gene_variant MELA-AU 10 35383598 35383598 single base substitution G A upstream_gene_variant MELA-AU 10 35383687 35383687 single base substitution A T upstream_gene_variant MELA-AU 10 35384035 35384035 single base substitution G A upstream_gene_variant MELA-AU 10 35384260 35384260 single base substitution A T upstream_gene_variant ORCA-IN 10 35311007 35311007 single base substitution A T intron_variant ORCA-IN 10 35338119 35338119 single base substitution C G intron_variant ORCA-IN 10 35363571 35363571 single base substitution C T intron_variant ORCA-IN 10 35363571 35363571 single base substitution C T upstream_gene_variant ORCA-IN 10 35370649 35370649 single base substitution C T intron_variant OV-AU 10 35294232 35294232 single base substitution C T downstream_gene_variant OV-AU 10 35296110 35296110 single base substitution G T downstream_gene_variant OV-AU 10 35308621 35308621 single base substitution G T intron_variant OV-AU 10 35309094 35309094 single base substitution T A intron_variant OV-AU 10 35318570 35318570 single base substitution T G splice_acceptor_variant OV-AU 10 35329720 35329720 single base substitution G A downstream_gene_variant OV-AU 10 35329720 35329720 single base substitution G A intron_variant OV-AU 10 35331704 35331704 single base substitution T A downstream_gene_variant OV-AU 10 35331704 35331704 single base substitution T A intron_variant OV-AU 10 35333780 35333780 single base substitution C G 3_prime_UTR_variant OV-AU 10 35333780 35333780 single base substitution C G missense_variant D118H 352G>C OV-AU 10 35333780 35333780 single base substitution C G missense_variant D175H 523G>C OV-AU 10 35333780 35333780 single base substitution C G missense_variant D194H 580G>C OV-AU 10 35338416 35338416 single base substitution A G intron_variant OV-AU 10 35340323 35340323 single base substitution C A intron_variant OV-AU 10 35342787 35342787 single base substitution T G intron_variant OV-AU 10 35346517 35346517 single base substitution G T downstream_gene_variant OV-AU 10 35346517 35346517 single base substitution G T intron_variant OV-AU 10 35349859 35349859 single base substitution T C downstream_gene_variant OV-AU 10 35349859 35349859 single base substitution T C exon_variant OV-AU 10 35349859 35349859 single base substitution T C missense_variant Y106C 317A>G OV-AU 10 35349859 35349859 single base substitution T C missense_variant Y87C 260A>G OV-AU 10 35349859 35349859 single base substitution T C splice_region_variant OV-AU 10 35351329 35351329 single base substitution G T downstream_gene_variant OV-AU 10 35351329 35351329 single base substitution G T intron_variant OV-AU 10 35352180 35352180 single base substitution C A downstream_gene_variant OV-AU 10 35352180 35352180 single base substitution C A intron_variant OV-AU 10 35353510 35353510 single base substitution C T intron_variant OV-AU 10 35366401 35366401 single base substitution G C intron_variant OV-AU 10 35366401 35366401 single base substitution G C upstream_gene_variant OV-AU 10 35374045 35374045 single base substitution C G intron_variant OV-AU 10 35379633 35379633 single base substitution G A upstream_gene_variant OV-US 10 35328011 35328011 single base substitution C T splice_acceptor_variant PACA-AU 10 35298420 35298420 single base substitution C T 3_prime_UTR_variant PACA-AU 10 35298420 35298420 single base substitution C T downstream_gene_variant PACA-AU 10 35306762 35306762 single base substitution A C intron_variant PACA-AU 10 35308143 35308143 single base substitution G A intron_variant PACA-AU 10 35312684 35312684 deletion of <=200bp G - intron_variant PACA-AU 10 35313800 35313800 single base substitution A C intron_variant PACA-AU 10 35315320 35315320 single base substitution A G intron_variant PACA-AU 10 35323742 35323742 single base substitution C T intron_variant PACA-AU 10 35327107 35327107 single base substitution C T intron_variant PACA-AU 10 35327326 35327326 single base substitution C T intron_variant PACA-AU 10 35334112 35334112 single base substitution C G intron_variant PACA-AU 10 35340519 35340519 single base substitution C T intron_variant PACA-AU 10 35348800 35348800 single base substitution C G downstream_gene_variant PACA-AU 10 35348800 35348800 single base substitution C G intron_variant PACA-AU 10 35353933 35353933 deletion of <=200bp T - intron_variant PACA-AU 10 35366257 35366258 deletion of <=200bp AC - intron_variant PACA-AU 10 35366257 35366258 deletion of <=200bp AC - upstream_gene_variant PACA-AU 10 35369362 35369362 insertion of <=200bp - TTTA intron_variant PACA-AU 10 35369976 35369976 single base substitution T A intron_variant PACA-AU 10 35382605 35382605 single base substitution A G upstream_gene_variant PACA-CA 10 35295632 35295632 insertion of <=200bp - T downstream_gene_variant PACA-CA 10 35298421 35298421 single base substitution G A 3_prime_UTR_variant PACA-CA 10 35298421 35298421 single base substitution G A downstream_gene_variant PACA-CA 10 35302591 35302591 single base substitution C T intron_variant PACA-CA 10 35303499 35303499 single base substitution G A intron_variant PACA-CA 10 35307232 35307232 single base substitution A C intron_variant PACA-CA 10 35308002 35308002 single base substitution T A intron_variant PACA-CA 10 35308008 35308008 single base substitution T G intron_variant PACA-CA 10 35309705 35309710 deletion of <=200bp TTCCTT - intron_variant PACA-CA 10 35309712 35309721 deletion of <=200bp TCGTTAATTC - intron_variant PACA-CA 10 35311770 35311770 single base substitution C T intron_variant PACA-CA 10 35314079 35314079 single base substitution C T 3_prime_UTR_variant PACA-CA 10 35314079 35314079 single base substitution C T stop_gained W498* 1494G>A PACA-CA 10 35314079 35314079 single base substitution C T stop_gained W555* 1665G>A PACA-CA 10 35314079 35314079 single base substitution C T stop_gained W574* 1722G>A PACA-CA 10 35322802 35322802 single base substitution A G intron_variant PACA-CA 10 35323130 35323130 single base substitution C T intron_variant PACA-CA 10 35324052 35324052 single base substitution G A intron_variant PACA-CA 10 35324681 35324681 single base substitution T C intron_variant PACA-CA 10 35324918 35324918 single base substitution C G intron_variant PACA-CA 10 35325213 35325213 single base substitution C T intron_variant PACA-CA 10 35326223 35326223 single base substitution G A intron_variant PACA-CA 10 35326788 35326788 single base substitution A G intron_variant PACA-CA 10 35329477 35329477 single base substitution T C downstream_gene_variant PACA-CA 10 35329477 35329477 single base substitution T C intron_variant PACA-CA 10 35333640 35333640 single base substitution A G intron_variant PACA-CA 10 35336155 35336155 single base substitution T A intron_variant PACA-CA 10 35338758 35338758 insertion of <=200bp - T intron_variant PACA-CA 10 35339032 35339032 single base substitution C T intron_variant PACA-CA 10 35339325 35339325 single base substitution C G intron_variant PACA-CA 10 35341835 35341835 single base substitution G A intron_variant PACA-CA 10 35342546 35342546 single base substitution G C intron_variant PACA-CA 10 35347046 35347046 single base substitution A T downstream_gene_variant PACA-CA 10 35347046 35347046 single base substitution A T intron_variant PACA-CA 10 35352103 35352103 single base substitution T G downstream_gene_variant PACA-CA 10 35352103 35352103 single base substitution T G intron_variant PACA-CA 10 35357859 35357859 single base substitution G A intron_variant PACA-CA 10 35365822 35365822 insertion of <=200bp - A intron_variant PACA-CA 10 35365822 35365822 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 35366263 35366263 insertion of <=200bp - C intron_variant PACA-CA 10 35366263 35366263 insertion of <=200bp - C upstream_gene_variant PACA-CA 10 35367130 35367130 single base substitution T C intron_variant PACA-CA 10 35367130 35367130 single base substitution T C upstream_gene_variant PACA-CA 10 35369690 35369690 single base substitution T C intron_variant PACA-CA 10 35371984 35371984 single base substitution C A intron_variant PACA-CA 10 35376136 35376136 single base substitution C T intron_variant PACA-CA 10 35383687 35383687 single base substitution A T upstream_gene_variant PACA-CA 10 35384187 35384187 insertion of <=200bp - ATTGCA upstream_gene_variant PACA-CA 10 35384491 35384491 single base substitution G A upstream_gene_variant PAEN-AU 10 35321933 35321933 single base substitution T G intron_variant PAEN-AU 10 35326300 35326300 single base substitution G A intron_variant PAEN-AU 10 35334601 35334601 single base substitution C T intron_variant PAEN-AU 10 35379513 35379513 single base substitution A C 5_prime_UTR_variant PAEN-AU 10 35379513 35379513 single base substitution A C upstream_gene_variant PAEN-IT 10 35297815 35297815 single base substitution A T 3_prime_UTR_variant PAEN-IT 10 35297815 35297815 single base substitution A T downstream_gene_variant PAEN-IT 10 35354661 35354661 single base substitution C T intron_variant PBCA-DE 10 35293394 35293394 single base substitution G A downstream_gene_variant PBCA-DE 10 35301478 35301478 single base substitution C T intron_variant PBCA-DE 10 35303117 35303117 insertion of <=200bp - T intron_variant PBCA-DE 10 35316491 35316491 deletion of <=200bp C - intron_variant PBCA-DE 10 35333614 35333614 single base substitution T C intron_variant PBCA-DE 10 35344044 35344044 single base substitution C A intron_variant PBCA-DE 10 35359817 35359817 insertion of <=200bp - T intron_variant PBCA-DE 10 35367417 35367417 single base substitution C T intron_variant PBCA-DE 10 35367417 35367417 single base substitution C T upstream_gene_variant PBCA-DE 10 35369300 35369300 single base substitution G C intron_variant PBCA-DE 10 35376769 35376769 single base substitution T C intron_variant PBCA-DE 10 35376800 35376800 single base substitution T C intron_variant PBCA-DE 10 35381604 35381604 single base substitution C A upstream_gene_variant PBCA-DE 10 35383684 35383684 single base substitution A C upstream_gene_variant PRAD-CA 10 35292584 35292584 single base substitution C T downstream_gene_variant PRAD-CA 10 35299911 35299911 single base substitution T C intron_variant PRAD-CA 10 35306504 35306504 single base substitution C A intron_variant PRAD-CA 10 35315486 35315486 single base substitution A G intron_variant PRAD-CA 10 35361166 35361166 single base substitution A C intron_variant PRAD-CA 10 35361166 35361166 single base substitution A C upstream_gene_variant PRAD-UK 10 35299954 35299954 single base substitution C A intron_variant PRAD-UK 10 35304571 35304586 deletion of <=200bp AGAAAAAAAGTTACAG - intron_variant PRAD-UK 10 35312322 35312322 single base substitution T G intron_variant PRAD-UK 10 35346961 35346961 single base substitution T C downstream_gene_variant PRAD-UK 10 35346961 35346961 single base substitution T C intron_variant PRAD-UK 10 35349902 35349902 single base substitution T C downstream_gene_variant PRAD-UK 10 35349902 35349902 single base substitution T C intron_variant PRAD-UK 10 35349902 35349902 single base substitution T C splice_region_variant PRAD-UK 10 35353859 35353859 single base substitution G C intron_variant PRAD-UK 10 35372144 35372144 single base substitution G T intron_variant PRAD-US 10 35318439 35318439 single base substitution T G 3_prime_UTR_variant PRAD-US 10 35318439 35318439 single base substitution T G missense_variant S449R 1345A>C PRAD-US 10 35318439 35318439 single base substitution T G missense_variant S506R 1516A>C PRAD-US 10 35318439 35318439 single base substitution T G missense_variant S525R 1573A>C PRAD-US 10 35351967 35351967 single base substitution G A downstream_gene_variant PRAD-US 10 35351967 35351967 single base substitution G A exon_variant PRAD-US 10 35351967 35351967 single base substitution G A missense_variant A48V 143C>T PRAD-US 10 35351967 35351967 single base substitution G A missense_variant A67V 200C>T PRAD-US 10 35351967 35351967 single base substitution G A missense_variant P6S 16C>T READ-US 10 35299245 35299245 single base substitution G A 3_prime_UTR_variant READ-US 10 35299245 35299245 single base substitution G A synonymous_variant V687V 2061C>T READ-US 10 35299245 35299245 single base substitution G A synonymous_variant V705V 2115C>T READ-US 10 35299245 35299245 single base substitution G A synonymous_variant V744V 2232C>T READ-US 10 35299245 35299245 single base substitution G A synonymous_variant V763V 2289C>T READ-US 10 35300826 35300826 single base substitution G A 3_prime_UTR_variant READ-US 10 35300826 35300826 single base substitution G A intron_variant READ-US 10 35300826 35300826 single base substitution G A missense_variant R629C 1885C>T READ-US 10 35300826 35300826 single base substitution G A missense_variant R686C 2056C>T READ-US 10 35300826 35300826 single base substitution G A missense_variant R705C 2113C>T READ-US 10 35327980 35327980 single base substitution G A 3_prime_UTR_variant READ-US 10 35327980 35327980 single base substitution G A stop_gained R192* 574C>T READ-US 10 35327980 35327980 single base substitution G A stop_gained R249* 745C>T READ-US 10 35327980 35327980 single base substitution G A stop_gained R268* 802C>T READ-US 10 35360133 35360133 single base substitution C T 5_prime_UTR_variant READ-US 10 35360133 35360133 single base substitution C T exon_variant READ-US 10 35360133 35360133 single base substitution C T missense_variant R38H 113G>A READ-US 10 35360133 35360133 single base substitution C T missense_variant R57H 170G>A RECA-EU 10 35297836 35297836 single base substitution A C 3_prime_UTR_variant RECA-EU 10 35297836 35297836 single base substitution A C downstream_gene_variant RECA-EU 10 35302502 35302502 single base substitution G A intron_variant RECA-EU 10 35313031 35313031 single base substitution G A intron_variant RECA-EU 10 35344001 35344001 single base substitution T G intron_variant RECA-EU 10 35352900 35352900 single base substitution T C exon_variant RECA-EU 10 35352900 35352900 single base substitution T C intron_variant RECA-EU 10 35356067 35356067 single base substitution C A intron_variant RECA-EU 10 35362675 35362675 single base substitution G A intron_variant RECA-EU 10 35362675 35362675 single base substitution G A upstream_gene_variant RECA-EU 10 35365810 35365810 single base substitution C T intron_variant RECA-EU 10 35365810 35365810 single base substitution C T upstream_gene_variant RECA-EU 10 35374921 35374921 single base substitution G T intron_variant RECA-EU 10 35383069 35383069 single base substitution A T upstream_gene_variant SKCA-BR 10 35292990 35292990 single base substitution G A downstream_gene_variant SKCA-BR 10 35297861 35297861 single base substitution A G 3_prime_UTR_variant SKCA-BR 10 35297861 35297861 single base substitution A G downstream_gene_variant SKCA-BR 10 35298129 35298129 insertion of <=200bp - TTA 3_prime_UTR_variant SKCA-BR 10 35298129 35298129 insertion of <=200bp - TTA downstream_gene_variant SKCA-BR 10 35301479 35301479 single base substitution G A intron_variant SKCA-BR 10 35302272 35302272 insertion of <=200bp - CA intron_variant SKCA-BR 10 35303694 35303694 single base substitution G A intron_variant SKCA-BR 10 35304984 35304984 single base substitution G C intron_variant SKCA-BR 10 35307691 35307691 insertion of <=200bp - CA intron_variant SKCA-BR 10 35308854 35308854 single base substitution G A intron_variant SKCA-BR 10 35311004 35311006 deletion of <=200bp CGT - intron_variant SKCA-BR 10 35311007 35311007 single base substitution A T intron_variant SKCA-BR 10 35316071 35316072 deletion of <=200bp CT - intron_variant SKCA-BR 10 35317991 35317991 insertion of <=200bp - GT intron_variant SKCA-BR 10 35321507 35321507 single base substitution C A intron_variant SKCA-BR 10 35325731 35325731 single base substitution G A intron_variant SKCA-BR 10 35327065 35327065 single base substitution G A intron_variant SKCA-BR 10 35327122 35327122 single base substitution T C intron_variant SKCA-BR 10 35328059 35328059 single base substitution G A intron_variant SKCA-BR 10 35334150 35334150 single base substitution C T intron_variant SKCA-BR 10 35334330 35334330 insertion of <=200bp - TAGAGC intron_variant SKCA-BR 10 35334473 35334473 insertion of <=200bp - CA intron_variant SKCA-BR 10 35337529 35337529 single base substitution G A intron_variant SKCA-BR 10 35339429 35339430 deletion of <=200bp CG - intron_variant SKCA-BR 10 35339434 35339434 single base substitution A T intron_variant SKCA-BR 10 35345626 35345626 single base substitution G A downstream_gene_variant SKCA-BR 10 35345626 35345626 single base substitution G A intron_variant SKCA-BR 10 35347269 35347269 single base substitution A C downstream_gene_variant SKCA-BR 10 35347269 35347269 single base substitution A C intron_variant SKCA-BR 10 35351418 35351418 single base substitution G A downstream_gene_variant SKCA-BR 10 35351418 35351418 single base substitution G A intron_variant SKCA-BR 10 35351598 35351598 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 10 35351598 35351598 insertion of <=200bp - CA intron_variant SKCA-BR 10 35357148 35357148 single base substitution G A intron_variant SKCA-BR 10 35357644 35357644 single base substitution G A intron_variant SKCA-BR 10 35357762 35357762 single base substitution G A intron_variant SKCA-BR 10 35366129 35366129 single base substitution G A intron_variant SKCA-BR 10 35366129 35366129 single base substitution G A upstream_gene_variant SKCA-BR 10 35371184 35371184 single base substitution A G intron_variant SKCA-BR 10 35372082 35372082 insertion of <=200bp - CA intron_variant SKCA-BR 10 35374362 35374367 deletion of <=200bp AAAAAT - intron_variant SKCA-BR 10 35374627 35374627 single base substitution A C intron_variant SKCA-BR 10 35375344 35375344 single base substitution C T intron_variant SKCA-BR 10 35380485 35380485 single base substitution C T upstream_gene_variant SKCA-BR 10 35381121 35381121 single base substitution G A upstream_gene_variant SKCA-BR 10 35381476 35381476 single base substitution G A upstream_gene_variant SKCA-BR 10 35383530 35383530 single base substitution C T upstream_gene_variant SKCA-BR 10 35384266 35384266 single base substitution G A upstream_gene_variant SKCA-BR 10 35384534 35384534 single base substitution T G upstream_gene_variant SKCM-US 10 35324198 35324198 single base substitution G A 3_prime_UTR_variant SKCM-US 10 35324198 35324198 single base substitution G A missense_variant R245C 733C>T SKCM-US 10 35324198 35324198 single base substitution G A missense_variant R302C 904C>T SKCM-US 10 35324198 35324198 single base substitution G A missense_variant R321C 961C>T SKCM-US 10 35328007 35328007 single base substitution G A 3_prime_UTR_variant SKCM-US 10 35328007 35328007 single base substitution G A synonymous_variant L183L 547C>T SKCM-US 10 35328007 35328007 single base substitution G A synonymous_variant L240L 718C>T SKCM-US 10 35328007 35328007 single base substitution G A synonymous_variant L259L 775C>T SKCM-US 10 35349802 35349802 single base substitution C T downstream_gene_variant SKCM-US 10 35349802 35349802 single base substitution C T exon_variant SKCM-US 10 35349802 35349802 single base substitution C T missense_variant R106K 317G>A SKCM-US 10 35349802 35349802 single base substitution C T missense_variant R125K 374G>A SKCM-US 10 35349802 35349802 single base substitution C T missense_variant R49K 146G>A SKCM-US 10 35349802 35349802 single base substitution C T splice_region_variant STAD-US 10 35299267 35299267 single base substitution G A 3_prime_UTR_variant STAD-US 10 35299267 35299267 single base substitution G A missense_variant S680L 2039C>T STAD-US 10 35299267 35299267 single base substitution G A missense_variant S698L 2093C>T STAD-US 10 35299267 35299267 single base substitution G A missense_variant S737L 2210C>T STAD-US 10 35299267 35299267 single base substitution G A missense_variant S756L 2267C>T STAD-US 10 35300856 35300856 single base substitution G A 3_prime_UTR_variant STAD-US 10 35300856 35300856 single base substitution G A intron_variant STAD-US 10 35300856 35300856 single base substitution G A missense_variant R619W 1855C>T STAD-US 10 35300856 35300856 single base substitution G A missense_variant R676W 2026C>T STAD-US 10 35300856 35300856 single base substitution G A missense_variant R695W 2083C>T STAD-US 10 35317808 35317808 single base substitution G T 3_prime_UTR_variant STAD-US 10 35317808 35317808 single base substitution G T missense_variant A459E 1376C>A STAD-US 10 35317808 35317808 single base substitution G T missense_variant A516E 1547C>A STAD-US 10 35317808 35317808 single base substitution G T missense_variant A535E 1604C>A STAD-US 10 35351916 35351916 deletion of <=200bp A - downstream_gene_variant STAD-US 10 35351916 35351916 deletion of <=200bp A - exon_variant STAD-US 10 35351916 35351916 deletion of <=200bp A - frameshift_variant L65 STAD-US 10 35351916 35351916 deletion of <=200bp A - frameshift_variant L84 STAD-US 10 35351916 35351916 deletion of <=200bp A - frameshift_variant W23 STAD-US 10 35351916 35351916 insertion of <=200bp - A downstream_gene_variant STAD-US 10 35351916 35351916 insertion of <=200bp - A exon_variant STAD-US 10 35351916 35351916 insertion of <=200bp - A frameshift_variant L65F? STAD-US 10 35351916 35351916 insertion of <=200bp - A frameshift_variant L84F? STAD-US 10 35351916 35351916 insertion of <=200bp - A frameshift_variant W23L? STAD-US 10 35360229 35360229 single base substitution C T 5_prime_UTR_variant STAD-US 10 35360229 35360229 single base substitution C T exon_variant STAD-US 10 35360229 35360229 single base substitution C T missense_variant R25K 74G>A STAD-US 10 35360229 35360229 single base substitution C T missense_variant R6K 17G>A THCA-SA 10 35299085 35299085 single base substitution C T 3_prime_UTR_variant THCA-SA 10 35299085 35299085 single base substitution C T downstream_gene_variant THCA-SA 10 35302705 35302705 single base substitution C T 3_prime_UTR_variant THCA-SA 10 35302705 35302705 single base substitution C T synonymous_variant S580S 1740G>A THCA-SA 10 35302705 35302705 single base substitution C T synonymous_variant S637S 1911G>A THCA-SA 10 35302705 35302705 single base substitution C T synonymous_variant S656S 1968G>A UCEC-US 10 35300793 35300793 single base substitution T A 3_prime_UTR_variant UCEC-US 10 35300793 35300793 single base substitution T A intron_variant UCEC-US 10 35300793 35300793 single base substitution T A missense_variant N640Y 1918A>T UCEC-US 10 35300793 35300793 single base substitution T A missense_variant N697Y 2089A>T UCEC-US 10 35300793 35300793 single base substitution T A missense_variant N716Y 2146A>T UCEC-US 10 35305157 35305157 single base substitution A G 3_prime_UTR_variant UCEC-US 10 35305157 35305157 single base substitution A G missense_variant L560S 1679T>C UCEC-US 10 35305157 35305157 single base substitution A G missense_variant L617S 1850T>C UCEC-US 10 35305157 35305157 single base substitution A G missense_variant L636S 1907T>C UCEC-US 10 35305249 35305251 deletion of <=200bp AAG - 3_prime_UTR_variant UCEC-US 10 35305249 35305251 deletion of <=200bp AAG - inframe_deletion L529 UCEC-US 10 35305249 35305251 deletion of <=200bp AAG - inframe_deletion L586 UCEC-US 10 35305249 35305251 deletion of <=200bp AAG - inframe_deletion L605 UCEC-US 10 35305275 35305275 single base substitution T C 3_prime_UTR_variant UCEC-US 10 35305275 35305275 single base substitution T C missense_variant T521A 1561A>G UCEC-US 10 35305275 35305275 single base substitution T C missense_variant T578A 1732A>G UCEC-US 10 35305275 35305275 single base substitution T C missense_variant T597A 1789A>G UCEC-US 10 35314080 35314080 single base substitution C A 3_prime_UTR_variant UCEC-US 10 35314080 35314080 single base substitution C A missense_variant W498L 1493G>T UCEC-US 10 35314080 35314080 single base substitution C A missense_variant W555L 1664G>T UCEC-US 10 35314080 35314080 single base substitution C A missense_variant W574L 1721G>T UCEC-US 10 35320284 35320284 single base substitution T A 3_prime_UTR_variant UCEC-US 10 35320284 35320284 single base substitution T A missense_variant I387F 1159A>T UCEC-US 10 35320284 35320284 single base substitution T A missense_variant I444F 1330A>T UCEC-US 10 35320284 35320284 single base substitution T A missense_variant I463F 1387A>T UCEC-US 10 35320512 35320512 single base substitution T C 3_prime_UTR_variant UCEC-US 10 35320512 35320512 single base substitution T C synonymous_variant S345S 1035A>G UCEC-US 10 35320512 35320512 single base substitution T C synonymous_variant S402S 1206A>G UCEC-US 10 35320512 35320512 single base substitution T C synonymous_variant S421S 1263A>G UCEC-US 10 35324169 35324169 single base substitution C T 3_prime_UTR_variant UCEC-US 10 35324169 35324169 single base substitution C T missense_variant M254I 762G>A UCEC-US 10 35324169 35324169 single base substitution C T missense_variant M311I 933G>A UCEC-US 10 35324169 35324169 single base substitution C T missense_variant M330I 990G>A UCEC-US 10 35327866 35327866 single base substitution G A 3_prime_UTR_variant UCEC-US 10 35327866 35327866 single base substitution G A stop_gained R230* 688C>T UCEC-US 10 35327866 35327866 single base substitution G A stop_gained R287* 859C>T UCEC-US 10 35327866 35327866 single base substitution G A stop_gained R306* 916C>T UCEC-US 10 35327920 35327920 single base substitution G A 3_prime_UTR_variant UCEC-US 10 35327920 35327920 single base substitution G A stop_gained R212* 634C>T UCEC-US 10 35327920 35327920 single base substitution G A stop_gained R269* 805C>T UCEC-US 10 35327920 35327920 single base substitution G A stop_gained R288* 862C>T UCEC-US 10 35333532 35333532 single base substitution A C 3_prime_UTR_variant UCEC-US 10 35333532 35333532 single base substitution A C downstream_gene_variant UCEC-US 10 35333532 35333532 single base substitution A C missense_variant L169V 505T>G UCEC-US 10 35333532 35333532 single base substitution A C missense_variant L226V 676T>G UCEC-US 10 35333532 35333532 single base substitution A C missense_variant L245V 733T>G UCEC-US 10 35343422 35343422 single base substitution C T 3_prime_UTR_variant UCEC-US 10 35343422 35343422 single base substitution C T synonymous_variant A121A 363G>A UCEC-US 10 35343422 35343422 single base substitution C T synonymous_variant A140A 420G>A UCEC-US 10 35343422 35343422 single base substitution C T synonymous_variant A64A 192G>A UCEC-US 10 35351902 35351902 single base substitution G A downstream_gene_variant UCEC-US 10 35351902 35351902 single base substitution G A exon_variant UCEC-US 10 35351902 35351902 single base substitution G A missense_variant R70W 208C>T UCEC-US 10 35351902 35351902 single base substitution G A missense_variant R89W 265C>T UCEC-US 10 35351902 35351902 single base substitution G A synonymous_variant F27F 81C>T UCEC-US 10 35360156 35360156 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 10 35360156 35360156 single base substitution G A exon_variant UCEC-US 10 35360156 35360156 single base substitution G A synonymous_variant V30V 90C>T UCEC-US 10 35360156 35360156 single base substitution G A synonymous_variant V49V 147C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand P-Thy001 COSM5095057 c.61A>G p.I21V Substitution - Missense 10:35071257-35071257 - BRC44 COSM5027207 c.391G>C p.D131H Substitution - Missense 10:35054466-35054466 - TCGA-QA-A7B7-01 COSM4909915 c.545A>G p.H182R Substitution - Missense 10:35044830-35044830 - PD4099a COSM160278 c.1470C>G p.F490L Substitution - Missense 10:35029557-35029557 - BD176T COSM5494890 c.252G>T p.L84F Substitution - Missense 10:35062987-35062987 - SM-4AX85 COSM3751760 c.1911G>A p.S637S Substitution - coding silent 10:35013777-35013777 - TCGA-BR-8679-01 COSM4013944 c.2026C>T p.R676W Substitution - Missense 10:35011928-35011928 - BD124T COSM5492649 c.715-5delT p.? Unknown 10:35039087-35039087 - p1_II-2 COSM1738235 c.1684+9C>T p.? Unknown 10:35025123-35025123 - p1_II-2 COSM1738236 c.1684+8G>A p.? Unknown 10:35025124-35025124 - PT38 COSM5922803 c.148C>T p.P50S Substitution - Missense 10:35063034-35063034 - HCC064T COSM5809879 c.1651A>C p.R551R Substitution - coding silent 10:35025165-35025165 - CHC1731T COSM4792165 c.961G>C p.D321H Substitution - Missense 10:35035213-35035213 - AOCS-001-1-7 COSM4137971 c.523G>C p.D175H Substitution - Missense 10:35044852-35044852 - TCGA-Q2-A5QZ-01 COSM3985602 c.49C>G p.L17V Substitution - Missense 10:35071269-35071269 - CHC1052T COSM5348864 c.156A>G p.A52A Substitution - coding silent 10:35071219-35071219 - TCGA-B5-A0JY-01 COSM917879 c.208C>T p.R70W Substitution - Missense 10:35062974-35062974 - ZZUFHECRKL-G074T COSM4177649 c.1618-4A>T p.? Unknown 10:35025202-35025202 - TCGA-B5-A0JR-01 COSM917873 c.933G>A p.M311I Substitution - Missense 10:35035241-35035241 - 6481_CLM COSM5753477 c.860G>A p.R287Q Substitution - Missense 10:35038937-35038937 - S00935 COSM5663037 c.44A>G p.H15R Substitution - Missense 10:35071331-35071331 - p1_I-2 COSM1738235 c.1684+9C>T p.? Unknown 10:35025123-35025123 - TCGA-BR-8081-01 COSM4013943 c.2210C>T p.S737L Substitution - Missense 10:35010339-35010339 - TCGA-AX-A0J0-01 COSM917877 c.676T>G p.L226V Substitution - Missense 10:35044604-35044604 - TCGA-BH-A18G-01 COSM5831465 c.932delA p.N311fs*20 Deletion - Frameshift 10:35038922-35038922 - TCGA-61-2008-01 COSM79711 c.1572A>G p.S524S Substitution - coding silent 10:35028855-35028855 - TCGA-BS-A0UF-01 COSM917871 c.1330A>T p.I444F Substitution - Missense 10:35031356-35031356 - 416 COSM4431423 c.301A>G p.M101V Substitution - Missense 10:35060890-35060890 - PT38 COSM5922802 c.205C>T p.P69S Substitution - Missense 10:35063034-35063034 - BN23 COSM1603422 c.1774G>A p.E592K Substitution - Missense 10:35016305-35016305 - TCGA-D8-A1XK-01 COSM5831464 c.1457A>T p.Y486F Substitution - Missense 10:35029627-35029627 - TCGA-60-2713-01 COSM684431 c.945G>A p.L315L Substitution - coding silent 10:35035229-35035229 - TCGA-32-1982-01 COSM3397104 c.2174T>A p.L725Q Substitution - Missense 10:35010375-35010375 - TCGA-13-0893-01 COSM69332 c.715-1G>A p.? Unknown 10:35039083-35039083 - p1_I-1 COSM1738235 c.1684+9C>T p.? Unknown 10:35025123-35025123 - 587336 COSM1202678 c.1910C>T p.S637L Substitution - Missense 10:35013778-35013778 - TCGA-EI-6917-01 COSM5825636 c.170G>A p.R57H Substitution - Missense 10:35071205-35071205 - C086 COSM5529403 c.916C>T p.R306* Substitution - Nonsense 10:35038938-35038938 - TCGA-IR-A3LK-01 COSM3437447 c.718C>T p.L240L Substitution - coding silent 10:35039079-35039079 - TCGA-AX-A05Y-01 COSM917867 c.1850T>C p.L617S Substitution - Missense 10:35016229-35016229 - AOCS-094-6-X COSM4137972 c.260A>G p.Y87C Substitution - Missense 10:35060931-35060931 - TCGA-AD-6889-01 COSM5826704 c.1382G>A p.R461H Substitution - Missense 10:35031361-35031361 - LS174T COSM1955908 c.1323delA p.K441fs*3 Deletion - Frameshift 10:35031363-35031363 - 41P3 COSM3375459 c.1665G>A p.W555* Substitution - Nonsense 10:35025151-35025151 - 587342 COSM1202679 c.1887G>T p.K629N Substitution - Missense 10:35016192-35016192 - CHC1052T COSM3666739 c.99A>G p.A33A Substitution - coding silent 10:35071219-35071219 - TCGA-LP-A4AV-01 COSM4825505 c.223-1G>A p.? Unknown 10:35060969-35060969 - AOCS-104-1-6 COSM4137970 c.1387-2A>C p.? Unknown 10:35029642-35029642 - DLD1 COSM1955902 c.2056C>T p.R686C Substitution - Missense 10:35011898-35011898 - 9583_CLM COSM5753478 c.829T>C p.S277P Substitution - Missense 10:35039025-35039025 - ME009T COSM223398 c.891G>A p.M297I Substitution - Missense 10:35035283-35035283 - BK0019 COSM4186154 c.574G>C p.E192Q Substitution - Missense 10:35044801-35044801 - sysucc-692T COSM5763711 c.1304C>T p.T435M Substitution - Missense 10:35031543-35031543 - PTC-7C COSM3751760 c.1911G>A p.S637S Substitution - coding silent 10:35013777-35013777 - 2521259 COSM5895345 c.1817delA p.N606fs*5 Deletion - Frameshift 10:35016262-35016262 - S00945 COSM310414 c.218A>G p.H73R Substitution - Missense 10:35062964-35062964 - TCGA-GD-A3OP-01 COSM1297225 c.1603A>T p.K535* Substitution - Nonsense 10:35028824-35028824 - CHC1731T COSM5348888 c.1018G>C p.D340H Substitution - Missense 10:35035213-35035213 - TCGA-AD-6889-01 COSM1347680 c.1325G>A p.R442H Substitution - Missense 10:35031361-35031361 - TCGA-BR-4184-01 COSM4013945 c.1547C>A p.A516E Substitution - Missense 10:35028880-35028880 - TCGA-AM-5820-01 COSM5826700 c.1968G>A p.S656S Substitution - coding silent 10:35013777-35013777 - T12 COSM5341243 c.1449C>T p.S483S Substitution - coding silent 10:35029578-35029578 - PAPNNX COSM5004645 c.70G>A p.V24M Substitution - Missense 10:35071248-35071248 - TCGA-AM-5820-01 COSM3751760 c.1911G>A p.S637S Substitution - coding silent 10:35013777-35013777 - 587342 COSM1202680 c.551T>C p.V184A Substitution - Missense 10:35044824-35044824 - TCGA-AX-A0J0-01 COSM917874 c.859C>T p.R287* Substitution - Nonsense 10:35038938-35038938 - DLD1 COSM1347682 c.875delA p.N292fs*20 Deletion - Frameshift 10:35038922-35038922 - LS180 COSM1955908 c.1323delA p.K441fs*3 Deletion - Frameshift 10:35031363-35031363 - S02403 COSM5700331 c.1097A>T p.H366L Substitution - Missense 10:35033236-35033236 - TCGA-D5-6928-01 COSM5825635 c.802C>T p.R268* Substitution - Nonsense 10:35039052-35039052 - YUFERY COSM5370585 c.729A>G p.L243L Substitution - coding silent 10:35039068-35039068 - C086 COSM917874 c.859C>T p.R287* Substitution - Nonsense 10:35038938-35038938 - TCGA-BT-A20W-01 COSM415040 c.88G>A p.V30I Substitution - Missense 10:35071230-35071230 - ESCC-134T COSM3935044 c.786G>A p.V262V Substitution - coding silent 10:35039011-35039011 - p1_II-1 COSM1738235 c.1684+9C>T p.? Unknown 10:35025123-35025123 - TCGA-CA-6717-01 COSM5826703 c.1405T>C p.S469P Substitution - Missense 10:35031338-35031338 - TCGA-AC-A5XS-01 COSM5831466 c.661-1G>A p.? Unknown 10:35044677-35044677 - TCGA-BG-A0M4-01 COSM917870 c.1664G>T p.W555L Substitution - Missense 10:35025152-35025152 - ESCC_109 COSM5638806 c.223-1G>C p.? Unknown 10:35060969-35060969 - TCGA-AA-A010-01 COSM186331 c.745C>T p.R249* Substitution - Nonsense 10:35039052-35039052 - PD5934a COSM5801174 c.2114_2115insAGC p.S705>RA Complex - insertion inframe 10:35010434-35010435 - TCGA-OL-A5D8-01 COSM5831463 c.1714C>A p.L572I Substitution - Missense 10:35025159-35025159 - TCGA-AP-A0LD-01 COSM917878 c.363G>A p.A121A Substitution - coding silent 10:35054494-35054494 - ICGC_MB129 COSM1955921 c.604-10A>G p.? Unknown 10:35044686-35044686 - A9 COSM5349558 c.1675-4_1675-3insT p.? Unknown 10:35025201-35025202 - TCGA-GV-A40E-01 COSM3790762 c.161G>C p.G54A Substitution - Missense 10:35063021-35063021 - ESO-1481 COSM1249456 c.266G>T p.R89M Substitution - Missense 10:35060925-35060925 - EGC15 COSM5050169 c.87C>T p.Y29Y Substitution - coding silent 10:35071231-35071231 - TCGA-AC-A5XS-01 COSM4390803 c.604-1G>A p.? Unknown 10:35044677-35044677 - LS174T COSM1955900 c.2083C>T p.R695W Substitution - Missense 10:35011871-35011871 - TCGA-BR-6452-01 COSM4013946 c.17G>A p.R6K Substitution - Missense 10:35071301-35071301 - TCGA-D1-A15X-01 COSM917869 c.1732A>G p.T578A Substitution - Missense 10:35016347-35016347 - S00945 COSM310414 c.218A>G p.H73R Substitution - Missense 10:35062964-35062964 - TCGA-DK-A1A3-01 COSM415041 c.1561C>T p.Q521* Substitution - Nonsense 10:35028866-35028866 - SNU-C4 COSM4651787 c.2028G>A p.R676R Substitution - coding silent 10:35011926-35011926 - YUFERY COSM5370584 c.786A>G p.L262L Substitution - coding silent 10:35039068-35039068 - HT115 COSM917880 c.90C>T p.V30V Substitution - coding silent 10:35071228-35071228 - TCGA-AZ-6598-01 COSM5826701 c.1604C>T p.A535V Substitution - Missense 10:35028880-35028880 - TCGA-EJ-5494-01 COSM1128061 c.143C>T p.A48V Substitution - Missense 10:35063039-35063039 - 0029_CRUK_PC_0029_T1_DNA COSM5421103 c.223-6A>G p.? Unknown 10:35060974-35060974 - 230 COSM3730370 c.427G>A p.A143T Substitution - Missense 10:35049762-35049762 - sysucc-692T COSM5763712 c.1247C>T p.T416M Substitution - Missense 10:35031543-35031543 - 0029_CRUK_PC_0029_T1_DNA COSM5421102 c.280-6A>G p.? Unknown 10:35060974-35060974 - A9 COSM5349559 c.1618-4_1618-3insT p.? Unknown 10:35025201-35025202 - TCGA-AZ-4315-01 COSM5826702 c.1405T>G p.S469A Substitution - Missense 10:35031338-35031338 - pfg053T COSM4752660 c.1373T>G p.I458S Substitution - Missense 10:35031313-35031313 - T12 COSM5341242 c.1506C>T p.S502S Substitution - coding silent 10:35029578-35029578 - HCC026T COSM5817898 c.1661A>G p.K554R Substitution - Missense 10:35028823-35028823 - p1_I-2 COSM1738236 c.1684+8G>A p.? Unknown 10:35025124-35025124 - 55 COSM5014908 c.1194A>T p.L398F Substitution - Missense 10:35031596-35031596 - p1_I-1 COSM1738236 c.1684+8G>A p.? Unknown 10:35025124-35025124 - TCGA-EE-A180-06 COSM3437448 c.317G>A p.R106K Substitution - Missense 10:35060874-35060874 - p1_II-1 COSM1738236 c.1684+8G>A p.? Unknown 10:35025124-35025124 - TCGA-D8-A1XK-01 COSM3807112 c.1400A>T p.Y467F Substitution - Missense 10:35029627-35029627 - RK064_C01 COSM1627481 c.1502T>C p.I501T Substitution - Missense 10:35029525-35029525 - 19M COSM5578359 c.1481G>A p.R494Q Substitution - Missense 10:35029603-35029603 - PT49 COSM5935567 c.865G>A p.E289K Substitution - Missense 10:35038932-35038932 - TCGA-AZ-6598-01 COSM1202682 c.1547C>T p.A516V Substitution - Missense 10:35028880-35028880 - I2L-P19Ta-Tumor-Organoid COSM5359990 c.2180A>T p.D727V Substitution - Missense 10:35010369-35010369 - TCGA-BH-A18G-01 COSM1347682 c.875delA p.N292fs*20 Deletion - Frameshift 10:35038922-35038922 - T3021 COSM1955909 c.1305C>T p.Y435Y Substitution - coding silent 10:35031381-35031381 - D3 COSM5006732 c.775T>A p.Y259N Substitution - Missense 10:35039022-35039022 - 2521259 COSM5895344 c.1874delA p.N625fs*5 Deletion - Frameshift 10:35016262-35016262 - TCGA-A5-A0GP-01 COSM917877 c.676T>G p.L226V Substitution - Missense 10:35044604-35044604 - BD124T COSM5492648 c.772-5delT p.? Unknown 10:35039087-35039087 - LS180 COSM1955900 c.2083C>T p.R695W Substitution - Missense 10:35011871-35011871 - TCGA-C5-A1BQ-01 COSM4841805 c.496G>C p.E166Q Substitution - Missense 10:35049693-35049693 - 6481_CLM COSM5753476 c.917G>A p.R306Q Substitution - Missense 10:35038937-35038937 - TCGA-F5-6814-01 COSM5825635 c.802C>T p.R268* Substitution - Nonsense 10:35039052-35039052 - 585208 COSM325098 c.602A>C p.K201T Substitution - Missense 10:35044773-35044773 - LUAD-F00121 COSM365612 c.2189A>G p.Y730C Substitution - Missense 10:35010360-35010360 - S02403 COSM5700332 c.1040A>T p.H347L Substitution - Missense 10:35033236-35033236 - I2L-P19Ta-Tumor-Organoid COSM5359989 c.2237A>T p.D746V Substitution - Missense 10:35010369-35010369 - RMS2034 COSM5880610 c.1203G>T p.K401N Substitution - Missense 10:35031587-35031587 - TCGA-D5-6928-01 COSM186331 c.745C>T p.R249* Substitution - Nonsense 10:35039052-35039052 - TCGA-EI-6917-01 COSM3415008 c.113G>A p.R38H Substitution - Missense 10:35071205-35071205 - CHC1731T COSM4792165 c.961G>C p.D321H Substitution - Missense 10:35035213-35035213 - TCGA-KK-A59Z-01 COSM4876414 c.1516A>C p.S506R Substitution - Missense 10:35029511-35029511 - AOCS-094-1-1 COSM4137972 c.260A>G p.Y87C Substitution - Missense 10:35060931-35060931 - HCC099T COSM5816651 c.1931A>T p.H644L Substitution - Missense 10:35016205-35016205 - TCGA-AA-A01Q-01 COSM300044 c.194_195insT p.L65fs*10 Insertion - Frameshift 10:35062987-35062988 - ZZUFHECRKL-G074T COSM5445708 c.1675-4A>T p.? Unknown 10:35025202-35025202 - HCC026T COSM5817899 c.1604A>G p.K535R Substitution - Missense 10:35028823-35028823 - BD176T COSM5494891 c.195G>T p.L65F Substitution - Missense 10:35062987-35062987 - PCSI_0009_Pa_X COSM3375459 c.1665G>A p.W555* Substitution - Nonsense 10:35025151-35025151 - TCGA-AZ-4315-01 COSM1347678 c.1348T>G p.S450A Substitution - Missense 10:35031338-35031338 - T2938 COSM1955916 c.905G>A p.R302H Substitution - Missense 10:35035269-35035269 - HCC099T COSM5816652 c.1874A>T p.H625L Substitution - Missense 10:35016205-35016205 - CSCC-18-T COSM4477896 c.2137C>T p.P713S Substitution - Missense 10:35010412-35010412 - MINO COSM1739686 c.974G>A p.R325Q Substitution - Missense 10:35035200-35035200 - ESCC_109 COSM5638805 c.280-1G>C p.? Unknown 10:35060969-35060969 - 19M COSM5578360 c.1424G>A p.R475Q Substitution - Missense 10:35029603-35029603 - TCGA-AA-3966-01 COSM272554 c.1171C>T p.L391F Substitution - Missense 10:35031619-35031619 - CHC1052T COSM3666739 c.99A>G p.A33A Substitution - coding silent 10:35071219-35071219 - PD5934a COSM5801170 c.877+3_877+6delAAGT p.? Unknown 10:35038914-35038917 - 41T COSM3375459 c.1665G>A p.W555* Substitution - Nonsense 10:35025151-35025151 - TCGA-43-2578-01 COSM684429 c.513T>G p.R171R Substitution - coding silent 10:35044862-35044862 - TCGA-EI-6917-01 COSM3415007 c.2232C>T p.V744V Substitution - coding silent 10:35010317-35010317 - PT49 COSM5935566 c.922G>A p.E308K Substitution - Missense 10:35038932-35038932 - 587376 COSM1202681 c.1698G>T p.M566I Substitution - Missense 10:35016381-35016381 - TCGA-EI-6917-01 COSM5825633 c.2289C>T p.V763V Substitution - coding silent 10:35010317-35010317 - TCGA-CA-6717-01 COSM1347679 c.1348T>C p.S450P Substitution - Missense 10:35031338-35031338 - TCGA-F5-6814-01 COSM1955902 c.2056C>T p.R686C Substitution - Missense 10:35011898-35011898 - TCGA-BS-A0UV-01 COSM917880 c.90C>T p.V30V Substitution - coding silent 10:35071228-35071228 - TCGA-B5-A0JY-01 COSM917872 c.1206A>G p.S402S Substitution - coding silent 10:35031584-35031584 - TCGA-EE-A2GC-06 COSM3437446 c.904C>T p.R302C Substitution - Missense 10:35035270-35035270 - PD5934a COSM5801169 c.934+3_934+6delAAGT p.? Unknown 10:35038914-35038917 - S00945 COSM5664383 c.275A>G p.H92R Substitution - Missense 10:35062964-35062964 - TCGA-24-2267-01 COSM70343 c.299A>G p.Y100C Substitution - Missense 10:35060892-35060892 - HCT15 COSM1955902 c.2056C>T p.R686C Substitution - Missense 10:35011898-35011898 - A549 COSM1675159 c.709G>T p.E237* Substitution - Nonsense 10:35044571-35044571 - TCGA-D1-A102-01 COSM917876 c.752G>A p.R251Q Substitution - Missense 10:35039045-35039045 - TCGA-D1-A103-01 COSM917875 c.805C>T p.R269* Substitution - Nonsense 10:35038992-35038992 - RMS2034 COSM5880609 c.1260G>T p.K420N Substitution - Missense 10:35031587-35031587 - PD5934a COSM5801173 c.2171_2172insAGC p.S724>RA Complex - insertion inframe 10:35010434-35010435 - TCGA-F5-6814-01 COSM186331 c.745C>T p.R249* Substitution - Nonsense 10:35039052-35039052 - PR-05-839 COSM243915 c.1138G>C p.E380Q Substitution - Missense 10:35032467-35032467 - 587238 COSM1202682 c.1547C>T p.A516V Substitution - Missense 10:35028880-35028880 - TCGA-F5-6814-01 COSM5825634 c.2113C>T p.R705C Substitution - Missense 10:35011898-35011898 - TCGA-B0-5400-01 COSM465625 c.2194G>A p.E732K Substitution - Missense 10:35010355-35010355 - TCGA-BG-A0VZ-01 COSM917866 c.2089A>T p.N697Y Substitution - Missense 10:35011865-35011865 - TCGA-OL-A5D8-01 COSM3807111 c.1657C>A p.L553I Substitution - Missense 10:35025159-35025159 - TCGA-DW-7840-01 COSM3985601 c.957C>A p.I319I Substitution - coding silent 10:35035217-35035217 - 9583_CLM COSM5753479 c.772T>C p.S258P Substitution - Missense 10:35039025-35039025 - TCGA-D1-A17B-01 COSM917868 c.1756_1758delCTT p.L586delL Deletion - In frame 10:35016321-35016323 - HCC064T COSM5809878 c.1708A>C p.R570R Substitution - coding silent 10:35025165-35025165 - TCGA-EE-A2MS-06 COSM3437447 c.718C>T p.L240L Substitution - coding silent 10:35039079-35039079 - T3024 COSM1202682 c.1547C>T p.A516V Substitution - Missense 10:35028880-35028880 - BN23T COSM1603422 c.1774G>A p.E592K Substitution - Missense 10:35016305-35016305 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.82919 10p11.21 603135

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - InFrameDeletion p.L605delL c.1813_1815delCTT 10 35305249 UCEC A C Missense p.L245V c.733T>G 10 35333532 UCEC A C Synonymous p.R190R c.570T>G 10 35333790 LUSC A G Missense p.L636S c.1907T>C 10 35305157 UCEC A T Missense p.L744Q c.2231T>A 10 35299303 GBM C A Missense p.R108M c.323G>T 10 35349853 ESCA C A Missense p.R190L c.569G>T 10 35333791 LUAD C A Missense p.W166L c.497G>T 10 35338677 STAD C A Missense p.W574L c.1721G>T 10 35314080 UCEC C A Nonsense p.E266* c.796G>T 10 35327986 LUAD C A SpliceAcceptorSNV . c.564-1G>T 10 35333797 LUAD C G Missense p.D150H c.448G>C 10 35343394 BRCA C G Missense p.D264H c.790G>C 10 35327992 HNSC C G Missense p.M476I c.1428G>C 10 35320243 LUAD C T Missense p.E751K c.2251G>A 10 35299283 RCCC C T Missense p.M316I c.948G>A 10 35324211 CM C T Missense p.M330I c.990G>A 10 35324169 UCEC C T Missense p.R125K c.374G>A 10 35349802 CM C T Missense p.R695Q c.2084G>A 10 35300855 STAD C T Missense p.V49I c.145G>A 10 35360158 BLCA C T SpliceAcceptorSNV . c.772-1G>A 10 35328011 OV C T Synonymous p.L334L c.1002G>A 10 35324157 LUSC G A Missense p.A535V c.1604C>T 10 35317808 STAD G A Missense p.A67V c.200C>T 10 35351967 PRAD G A Missense p.R321C c.961C>T 10 35324198 CM G A Nonsense p.Q540* c.1618C>T 10 35317794 BLCA G A Synonymous p.L259L c.775C>T 10 35328007 CM G C Missense p.F509L c.1527C>G 10 35318485 BRCA GG AA Missense p.L142F c.423_424delinsTT 10 35343418 CM GG AA Missense p.P218L c.653_654delinsTT 10 35333706 CM T A Missense p.N716Y c.2146A>T 10 35300793 UCEC T A Missense p.S114C c.340A>T 10 35349836 LUAD T A Nonsense p.K554* c.1660A>T 10 35317752 BLCA T C Missense p.H92R c.275A>G 10 35351892 SCLC T C Missense p.Y119C c.356A>G 10 35349820 OV T C Synonymous p.R75R c.225A>G 10 35351942 CM T C Synonymous p.S543S c.1629A>G 10 35317783 OV T - Frameshift p.N311Mfs*20 c.932delA 10 35327850 PRAD T G Missense p.K220T c.659A>C 10 35333701 SCLC T G Missense p.S525R c.1573A>C 10 35318439 PRAD