Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 4 153249473 153249473 + Silent SNP A A G TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr4:153249473A>G c.1305T>C c.(1303-1305)atT>atC p.I435I BLCA 4 153244124 153244124 + Nonsense_Mutation SNP G G C TCGA-DK-A2I2-01A-11D-A17V-08 TCGA-DK-A2I2-10A-01D-A17V-08 g.chr4:153244124G>C c.2033C>G c.(2032-2034)tCa>tGa p.S678* BLCA 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* BLCA 4 153244232 153244232 + Missense_Mutation SNP T T C TCGA-GC-A3RD-01A-12D-A22Z-08 TCGA-GC-A3RD-10B-01D-A22Z-08 g.chr4:153244232T>C c.1925A>G c.(1924-1926)gAt>gGt p.D642G BLCA 4 153244235 153244235 + Nonsense_Mutation SNP G G C TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr4:153244235G>C c.1922C>G c.(1921-1923)tCa>tGa p.S641* BLCA 4 153245449 153245450 + Frame_Shift_Ins INS - - G TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr4:153245449_153245450insG c.1741_1742insC c.(1741-1743)cagfs p.Q581fs BLCA 4 153247165 153247165 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:153247165G>A c.1637C>T c.(1636-1638)tCa>tTa p.S546L BLCA 4 153247165 153247165 + Missense_Mutation SNP G G A TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr4:153247165G>A c.1637C>T c.(1636-1638)tCa>tTa p.S546L BLCA 4 153247244 153247244 + Missense_Mutation SNP C C T TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr4:153247244C>T c.1558G>A c.(1558-1560)Gat>Aat p.D520N BLCA 4 153247253 153247253 + Missense_Mutation SNP C C T TCGA-XF-A9T2-01A-11D-A42E-08 TCGA-XF-A9T2-10A-01D-A42H-08 g.chr4:153247253C>T c.1549G>A c.(1549-1551)Gga>Aga p.G517R BLCA 4 153247280 153247280 + Nonsense_Mutation SNP G G A TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr4:153247280G>A c.1522C>T c.(1522-1524)Caa>Taa p.Q508* BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-BL-A13I-01A-11D-A13W-08 TCGA-BL-A13I-11A-11D-A13W-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-C4-A0F1-01A-11D-A10S-08 TCGA-C4-A0F1-10A-01D-A10S-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-DK-A3WX-01A-22D-A22Z-08 TCGA-DK-A3WX-10A-01D-A22Z-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-FD-A6TF-01A-52D-A32B-08 TCGA-FD-A6TF-10A-21D-A329-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-YC-A9TC-01A-22D-A391-08 TCGA-YC-A9TC-10A-01D-A394-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G BLCA 4 153247366 153247366 + Missense_Mutation SNP C C G TCGA-BT-A20O-01A-21D-A14W-08 TCGA-BT-A20O-11A-11D-A14W-08 g.chr4:153247366C>G c.1436G>C c.(1435-1437)cGa>cCa p.R479P BLCA 4 153247367 153247367 + Missense_Mutation SNP G G C TCGA-4Z-AA7O-01A-31D-A391-08 TCGA-4Z-AA7O-10A-01D-A394-08 g.chr4:153247367G>C c.1435C>G c.(1435-1437)Cga>Gga p.R479G BLCA 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* BLCA 4 153249367 153249367 + Frame_Shift_Del DEL C C - TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr4:153249367delC c.1411delG c.(1411-1413)gaafs p.E471fs BLCA 4 153249370 153249370 + Missense_Mutation SNP G G A TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr4:153249370G>A c.1408C>T c.(1408-1410)Cat>Tat p.H470Y BLCA 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-E7-A5KE-01A-11D-A289-08 TCGA-E7-A5KE-10A-01D-A289-08 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C BLCA 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-XF-AAN1-01A-31D-A42E-08 TCGA-XF-AAN1-10A-01D-A42H-08 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C BLCA 4 153249501 153249501 + Missense_Mutation SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr4:153249501G>A c.1277C>T c.(1276-1278)tCa>tTa p.S426L BLCA 4 153250865 153250865 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr4:153250865C>G c.1195G>C c.(1195-1197)Gat>Cat p.D399H BLCA 4 153250906 153250906 + Missense_Mutation SNP G G T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr4:153250906G>T c.1154C>A c.(1153-1155)aCa>aAa p.T385K BLCA 4 153251911 153251911 + Nonsense_Mutation SNP C C T TCGA-PQ-A6FN-01A-11D-A31L-08 TCGA-PQ-A6FN-10A-01D-A31J-08 g.chr4:153251911C>T c.1095G>A c.(1093-1095)tgG>tgA p.W365* BLCA 4 153253770 153253770 + Nonsense_Mutation SNP C C T TCGA-C4-A0F0-01A-12D-A10S-08 TCGA-C4-A0F0-10A-01D-A10S-08 g.chr4:153253770C>T c.963G>A c.(961-963)tgG>tgA p.W321* BLCA 4 153253821 153253837 + Frame_Shift_Del DEL TGCTTGTAGCAGGTCTT TGCTTGTAGCAGGTCTT - TCGA-YC-A9TC-01A-22D-A391-08 TCGA-YC-A9TC-10A-01D-A394-08 g.chr4:153253821_153253837delTGCTTGTAGCAGGTCTT c.896_912delAAGACCTGCTACAAGCA c.(895-912)aaagacctgctacaagcafs p.KDLLQA299fs BLCA 4 153258983 153258983 + Nonsense_Mutation SNP G G A TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr4:153258983G>A c.832C>T c.(832-834)Cga>Tga p.R278* BLCA 4 153273634 153273634 + Intron SNP C C T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr4:153273634C>T BLCA 4 153273676 153273676 + Intron SNP C C T TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr4:153273676C>T BLCA 4 153273765 153273765 + Intron SNP C C T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr4:153273765C>T BLCA 4 153273859 153273859 + Intron SNP C C T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr4:153273859C>T BLCA 4 153273871 153273871 + Intron SNP C C T TCGA-LC-A66R-01A-41D-A30E-08 TCGA-LC-A66R-10A-01D-A30H-08 g.chr4:153273871C>T BLCA 4 153303406 153303406 + Intron SNP G G C TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr4:153303406G>C BLCA 4 153332524 153332524 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr4:153332524C>T c.432G>A c.(430-432)acG>acA p.T144T BLCA 4 153332577 153332577 + Nonsense_Mutation SNP G G A TCGA-GU-A42Q-01A-11D-A23U-08 TCGA-GU-A42Q-10A-01D-A23U-08 g.chr4:153332577G>A c.379C>T c.(379-381)Cag>Tag p.Q127* BLCA 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q BLCA 4 153332916 153332916 + Nonsense_Mutation SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr4:153332916G>A c.40C>T c.(40-42)Cga>Tga p.R14* BRCA 4 153244156 153244156 + Frame_Shift_Del DEL C C - TCGA-E2-A15L-01A-11D-A12B-09 TCGA-E2-A15L-11A-31D-A12B-09 g.chr4:153244156delC c.2001delG c.(1999-2001)gggfs p.G667fs BRCA 4 153247168 153247168 + Missense_Mutation SNP T T C TCGA-AR-A256-01A-11D-A167-09 TCGA-AR-A256-10A-01D-A167-09 g.chr4:153247168T>C c.1634A>G c.(1633-1635)tAt>tGt p.Y545C BRCA 4 153247265 153247265 + Missense_Mutation SNP T T C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr4:153247265T>C c.1537A>G c.(1537-1539)Agg>Ggg p.R513G BRCA 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-A2-A0D0-01A-11W-A019-09 TCGA-A2-A0D0-10A-01W-A021-09 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q BRCA 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-E2-A574-01A-11D-A29N-09 TCGA-E2-A574-10A-01D-A29N-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C BRCA 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-GM-A3XL-01A-11D-A22X-09 TCGA-GM-A3XL-10A-01D-A22X-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C BRCA 4 153250865 153250865 + Missense_Mutation SNP C C G TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr4:153250865C>G c.1195G>C c.(1195-1197)Gat>Cat p.D399H BRCA 4 153250888 153250888 + Missense_Mutation SNP C C T TCGA-E9-A22E-01A-11D-A159-09 TCGA-E9-A22E-10A-01D-A159-09 g.chr4:153250888C>T c.1172G>A c.(1171-1173)gGt>gAt p.G391D BRCA 4 153251936 153251936 + Missense_Mutation SNP C C T TCGA-EW-A1PE-01A-11D-A142-09 TCGA-EW-A1PE-10A-01D-A142-09 g.chr4:153251936C>T c.1070G>A c.(1069-1071)aGa>aAa p.R357K BRCA 4 153251995 153251995 + Silent SNP C C T TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr4:153251995C>T c.1011G>A c.(1009-1011)aaG>aaA p.K337K BRCA 4 153253808 153253808 + Frame_Shift_Del DEL G G - TCGA-A1-A0SP-01A-11D-A099-09 TCGA-A1-A0SP-10A-02D-A099-09 g.chr4:153253808delG c.925delC c.(925-927)cgcfs p.R309fs BRCA 4 153253831 153253831 + Missense_Mutation SNP A A G TCGA-A8-A09M-01A-11W-A019-09 TCGA-A8-A09M-10A-01W-A021-09 g.chr4:153253831A>G c.902T>C c.(901-903)cTg>cCg p.L301P BRCA 4 153271249 153271249 + Missense_Mutation SNP C C G TCGA-A2-A3XT-01A-11D-A22X-09 TCGA-A2-A3XT-10A-01D-A22X-09 g.chr4:153271249C>G c.529G>C c.(529-531)Gag>Cag p.E177Q BRCA 4 153271249 153271249 + Missense_Mutation SNP C C T TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr4:153271249C>T c.529G>A c.(529-531)Gag>Aag p.E177K BRCA 4 153332699 153332699 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr4:153332699G>A c.257C>T c.(256-258)tCg>tTg p.S86L BRCA 4 153332918 153332918 + Missense_Mutation SNP C C A TCGA-AC-A2QI-01A-12D-A19Y-09 TCGA-AC-A2QI-10A-01D-A19Y-09 g.chr4:153332918C>A c.38G>T c.(37-39)cGa>cTa p.R13L CESC 4 153244184 153244184 + Missense_Mutation SNP C C T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr4:153244184C>T c.1973G>A c.(1972-1974)cGa>cAa p.R658Q CESC 4 153244185 153244185 + Silent SNP G G T TCGA-C5-A1ML-01A-11D-A14W-08 TCGA-C5-A1ML-10A-01D-A14W-08 g.chr4:153244185G>T c.1972C>A c.(1972-1974)Cga>Aga p.R658R CESC 4 153245393 153245393 + Missense_Mutation SNP C C G TCGA-EK-A2R7-01A-11D-A18J-09 TCGA-EK-A2R7-10A-01D-A18J-09 g.chr4:153245393C>G c.1798G>C c.(1798-1800)Gat>Cat p.D600H CESC 4 153245393 153245393 + Missense_Mutation SNP C C T TCGA-C5-A1M9-01A-11D-A13W-08 TCGA-C5-A1M9-10A-01D-A13W-08 g.chr4:153245393C>T c.1798G>A c.(1798-1800)Gat>Aat p.D600N CESC 4 153247245 153247245 + Nonsense_Mutation SNP A A T TCGA-DS-A0VN-01A-21D-A10S-08 TCGA-DS-A0VN-10A-01D-A10S-08 g.chr4:153247245A>T c.1557T>A c.(1555-1557)taT>taA p.Y519* CESC 4 153247280 153247280 + Nonsense_Mutation SNP G G A TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr4:153247280G>A c.1522C>T c.(1522-1524)Caa>Taa p.Q508* CESC 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C CESC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-DS-A1OA-01A-11D-A16Y-08 TCGA-DS-A1OA-10A-01D-A16Y-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G CESC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G CESC 4 153247304 153247304 + Missense_Mutation SNP G G C TCGA-FU-A2QG-01A-11D-A18J-09 TCGA-FU-A2QG-10A-01D-A18J-09 g.chr4:153247304G>C c.1498C>G c.(1498-1500)Cat>Gat p.H500D CESC 4 153247366 153247366 + Missense_Mutation SNP C C G TCGA-C5-A1BJ-01A-11D-A13W-08 TCGA-C5-A1BJ-10A-01D-A13W-08 g.chr4:153247366C>G c.1436G>C c.(1435-1437)cGa>cCa p.R479P CESC 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-FU-A57G-01A-11D-A26G-09 TCGA-FU-A57G-10A-01D-A26G-09 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q CESC 4 153247367 153247367 + Missense_Mutation SNP G G C TCGA-EK-A2PL-01A-11D-A18J-09 TCGA-EK-A2PL-10A-01D-A18J-09 g.chr4:153247367G>C c.1435C>G c.(1435-1437)Cga>Gga p.R479G CESC 4 153249384 153249384 + Missense_Mutation SNP C C A TCGA-EK-A2RL-01A-11D-A18J-09 TCGA-EK-A2RL-10A-01D-A18J-09 g.chr4:153249384C>A c.1394G>T c.(1393-1395)cGt>cTt p.R465L CESC 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-FU-A5XV-01A-11D-A28B-09 TCGA-FU-A5XV-10A-01D-A28E-09 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H CESC 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-EA-A3HQ-01A-11D-A20U-09 TCGA-EA-A3HQ-10A-01D-A20U-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C CESC 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-EA-A3QE-01A-21D-A21Q-09 TCGA-EA-A3QE-10A-01D-A21Q-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C CESC 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-EK-A3GN-01A-11D-A20U-09 TCGA-EK-A3GN-10A-01D-A20U-09 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* CESC 4 153253770 153253770 + Nonsense_Mutation SNP C C T TCGA-EA-A50E-01A-21D-A26G-09 TCGA-EA-A50E-10A-01D-A26G-09 g.chr4:153253770C>T c.963G>A c.(961-963)tgG>tgA p.W321* CESC 4 153258986 153258986 + Missense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr4:153258986G>C c.829C>G c.(829-831)Caa>Gaa p.Q277E CESC 4 153268138 153268138 + Nonsense_Mutation SNP G G A TCGA-C5-A7CG-01A-11D-A32I-09 TCGA-C5-A7CG-10A-01D-A32I-09 g.chr4:153268138G>A c.670C>T c.(670-672)Cga>Tga p.R224* CHOL 4 153250882 153250882 + Missense_Mutation SNP C C T TCGA-W5-AA30-01A-31D-A417-09 TCGA-W5-AA30-10A-01D-A41A-09 g.chr4:153250882C>T c.1178G>A c.(1177-1179)cGa>cAa p.R393Q COAD 4 153244078 153244078 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COAD 4 153244078 153244078 + Silent SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COAD 4 153244078 153244078 + Silent SNP T T C TCGA-D5-7000-01A-11D-1924-10 TCGA-D5-7000-10A-01D-1924-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COAD 4 153244079 153244079 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr4:153244079T>C c.2078A>G c.(2077-2079)gAa>gGa p.E693G COAD 4 153244090 153244090 + Silent SNP C C T TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr4:153244090C>T c.2067G>A c.(2065-2067)cgG>cgA p.R689R COAD 4 153244091 153244091 + Missense_Mutation SNP C C A TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr4:153244091C>A c.2066G>T c.(2065-2067)cGg>cTg p.R689L COAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-AA-3524-01A-02W-0831-10 TCGA-AA-3524-10A-01W-0831-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COAD 4 153244136 153244136 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr4:153244136C>A c.2021G>T c.(2020-2022)cGg>cTg p.R674L COAD 4 153244141 153244141 + Silent SNP C C T TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153244141C>T c.2016G>A c.(2014-2016)gtG>gtA p.V672V COAD 4 153244156 153244156 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153244156delC c.2001delG c.(1999-2001)gggfs p.G667fs COAD 4 153244184 153244184 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr4:153244184C>T c.1973G>A c.(1972-1974)cGa>cAa p.R658Q COAD 4 153244184 153244184 + Missense_Mutation SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153244184C>T c.1973G>A c.(1972-1974)cGa>cAa p.R658Q COAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COAD 4 153244204 153244204 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr4:153244204C>T c.1953G>A c.(1951-1953)ttG>ttA p.L651L COAD 4 153244206 153244206 + Silent SNP A A G TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr4:153244206A>G c.1951T>C c.(1951-1953)Ttg>Ctg p.L651L COAD 4 153244210 153244210 + Nonsense_Mutation SNP C C T TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr4:153244210C>T c.1947G>A c.(1945-1947)tgG>tgA p.W649* COAD 4 153244280 153244280 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr4:153244280G>T c.1877C>A c.(1876-1878)gCt>gAt p.A626D COAD 4 153245343 153245343 + Silent SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr4:153245343T>A c.1848A>T c.(1846-1848)acA>acT p.T616T COAD 4 153245403 153245403 + Silent SNP A A T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr4:153245403A>T c.1788T>A c.(1786-1788)tcT>tcA p.S596S COAD 4 153245405 153245405 + Missense_Mutation SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr4:153245405A>G c.1786T>C c.(1786-1788)Tct>Cct p.S596P COAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-D5-7000-01A-11D-1924-10 TCGA-D5-7000-10A-01D-1924-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COAD 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AA-3831-01A-01W-0900-09 TCGA-AA-3831-10A-01W-0900-09 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L COAD 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L COAD 4 153245446 153245446 + Nonsense_Mutation SNP G G T TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr4:153245446G>T c.1745C>A c.(1744-1746)tCg>tAg p.S582* COAD 4 153245447 153245447 + Missense_Mutation SNP A A T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153245447A>T c.1744T>A c.(1744-1746)Tcg>Acg p.S582T COAD 4 153245450 153245450 + Nonsense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr4:153245450G>A c.1741C>T c.(1741-1743)Cag>Tag p.Q581* COAD 4 153245461 153245461 + Missense_Mutation SNP A A G TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr4:153245461A>G c.1730T>C c.(1729-1731)tTa>tCa p.L577S COAD 4 153247167 153247167 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr4:153247167A>G c.1635T>C c.(1633-1635)taT>taC p.Y545Y COAD 4 153247167 153247167 + Silent SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr4:153247167A>G c.1635T>C c.(1633-1635)taT>taC p.Y545Y COAD 4 153247168 153247168 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr4:153247168T>C c.1634A>G c.(1633-1635)tAt>tGt p.Y545C COAD 4 153247173 153247173 + Silent SNP T T C TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153247173T>C c.1629A>G c.(1627-1629)agA>agG p.R543R COAD 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A COAD 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A COAD 4 153247221 153247221 + Silent SNP A A G TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153247221A>G c.1581T>C c.(1579-1581)gaT>gaC p.D527D COAD 4 153247222 153247222 + Missense_Mutation SNP T T C TCGA-A6-5656-01A-21D-1835-10 TCGA-A6-5656-10A-01D-1835-10 g.chr4:153247222T>C c.1580A>G c.(1579-1581)gAt>gGt p.D527G COAD 4 153247223 153247223 + Missense_Mutation SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr4:153247223C>T c.1579G>A c.(1579-1581)Gat>Aat p.D527N COAD 4 153247244 153247244 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153247244C>A c.1558G>T c.(1558-1560)Gat>Tat p.D520Y COAD 4 153247244 153247244 + Missense_Mutation SNP C C T TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr4:153247244C>T c.1558G>A c.(1558-1560)Gat>Aat p.D520N COAD 4 153247288 153247288 + Missense_Mutation SNP C C A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153247288C>A c.1514G>T c.(1513-1515)cGc>cTc p.R505L COAD 4 153247288 153247288 + Missense_Mutation SNP C C T TCGA-AA-A024-01A-02W-A00E-09 TCGA-AA-A024-10A-01W-A00E-09 g.chr4:153247288C>T c.1514G>A c.(1513-1515)cGc>cAc p.R505H COAD 4 153247288 153247288 + Missense_Mutation SNP C C T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr4:153247288C>T c.1514G>A c.(1513-1515)cGc>cAc p.R505H COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-A6-3807-01A-01W-0995-10 TCGA-A6-3807-11A-01W-0995-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AA-3560-01A-01W-0831-10 TCGA-AA-3560-10A-01W-0831-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COAD 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-A6-2677-01A-01W-0831-10 TCGA-A6-2677-10A-01W-0831-10 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G COAD 4 153247289 153247289 + Missense_Mutation SNP G G T TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr4:153247289G>T c.1513C>A c.(1513-1515)Cgc>Agc p.R505S COAD 4 153247291 153247291 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr4:153247291A>G c.1511T>C c.(1510-1512)gTc>gCc p.V504A COAD 4 153247291 153247291 + Missense_Mutation SNP A A G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr4:153247291A>G c.1511T>C c.(1510-1512)gTc>gCc p.V504A COAD 4 153247345 153247345 + Missense_Mutation SNP C C A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153247345C>A c.1457G>T c.(1456-1458)tGg>tTg p.W486L COAD 4 153247351 153247351 + Missense_Mutation SNP C C A TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr4:153247351C>A c.1451G>T c.(1450-1452)aGg>aTg p.R484M COAD 4 153247363 153247363 + Missense_Mutation SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153247363T>C c.1439A>G c.(1438-1440)gAt>gGt p.D480G COAD 4 153247365 153247365 + Silent SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr4:153247365T>C c.1437A>G c.(1435-1437)cgA>cgG p.R479R COAD 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q COAD 4 153247367 153247367 + Missense_Mutation SNP G G C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr4:153247367G>C c.1435C>G c.(1435-1437)Cga>Gga p.R479G COAD 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* COAD 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-A6-6137-01A-11D-1771-10 TCGA-A6-6137-10A-01D-1806-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* COAD 4 153247374 153247374 + Missense_Mutation SNP G G T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr4:153247374G>T c.1428C>A c.(1426-1428)agC>agA p.S476R COAD 4 153249361 153249361 + Splice_Site DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr4:153249361delT c.1417delA c.(1417-1419)aga>ga p.R473fs COAD 4 153249383 153249383 + Silent SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COAD 4 153249383 153249383 + Silent SNP A A G TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COAD 4 153249384 153249384 + Missense_Mutation SNP C C G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr4:153249384C>G c.1394G>C c.(1393-1395)cGt>cCt p.R465P COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AA-3848-01A-01W-0900-09 TCGA-AA-3848-10A-01W-0900-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COAD 4 153249385 153249385 + Missense_Mutation SNP G G T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr4:153249385G>T c.1393C>A c.(1393-1395)Cgt>Agt p.R465S COAD 4 153249400 153249400 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr4:153249400G>A c.1378C>T c.(1378-1380)Cat>Tat p.H460Y COAD 4 153249440 153249440 + Nonsense_Mutation SNP C C T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr4:153249440C>T c.1338G>A c.(1336-1338)tgG>tgA p.W446* COAD 4 153249440 153249440 + Nonsense_Mutation SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153249440C>T c.1338G>A c.(1336-1338)tgG>tgA p.W446* COAD 4 153249441 153249441 + Nonsense_Mutation SNP C C T TCGA-F4-6704-01A-11D-1835-10 TCGA-F4-6704-11A-01D-1835-10 g.chr4:153249441C>T c.1337G>A c.(1336-1338)tGg>tAg p.W446* COAD 4 153249442 153249442 + Missense_Mutation SNP A A G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153249442A>G c.1336T>C c.(1336-1338)Tgg>Cgg p.W446R COAD 4 153249456 153249456 + Missense_Mutation SNP C C A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr4:153249456C>A c.1322G>T c.(1321-1323)cGg>cTg p.R441L COAD 4 153249457 153249457 + Missense_Mutation SNP G G A TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr4:153249457G>A c.1321C>T c.(1321-1323)Cgg>Tgg p.R441W COAD 4 153249457 153249457 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153249457G>A c.1321C>T c.(1321-1323)Cgg>Tgg p.R441W COAD 4 153249457 153249457 + Silent SNP G G T TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:153249457G>T c.1321C>A c.(1321-1323)Cgg>Agg p.R441R COAD 4 153249457 153249457 + Silent SNP G G T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr4:153249457G>T c.1321C>A c.(1321-1323)Cgg>Agg p.R441R COAD 4 153249465 153249465 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr4:153249465G>A c.1313C>T c.(1312-1314)tCt>tTt p.S438F COAD 4 153249465 153249465 + Missense_Mutation SNP G G T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr4:153249465G>T c.1313C>A c.(1312-1314)tCt>tAt p.S438Y COAD 4 153249509 153249509 + Silent SNP T T A TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr4:153249509T>A c.1269A>T c.(1267-1269)ggA>ggT p.G423G COAD 4 153249509 153249509 + Silent SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr4:153249509T>C c.1269A>G c.(1267-1269)ggA>ggG p.G423G COAD 4 153249510 153249510 + Missense_Mutation SNP C C A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr4:153249510C>A c.1268G>T c.(1267-1269)gGa>gTa p.G423V COAD 4 153249518 153249518 + Silent SNP A A G TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr4:153249518A>G c.1260T>C c.(1258-1260)caT>caC p.H420H COAD 4 153249518 153249519 + Frame_Shift_Ins INS - - TGTCCCAC TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr4:153249518_153249519insTGTCCCAC c.1259_1260insGTGGGACA c.(1258-1260)catfs p.H420fs COAD 4 153249519 153249519 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153249519T>C c.1259A>G c.(1258-1260)cAt>cGt p.H420R COAD 4 153249519 153249519 + Missense_Mutation SNP T T C TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr4:153249519T>C c.1259A>G c.(1258-1260)cAt>cGt p.H420R COAD 4 153250848 153250848 + Frame_Shift_Del DEL T T - TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr4:153250848delT c.1212delA c.(1210-1212)aaafs p.K404fs COAD 4 153250882 153250882 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153250882C>T c.1178G>A c.(1177-1179)cGa>cAa p.R393Q COAD 4 153250904 153250904 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:153250904A>T c.1156T>A c.(1156-1158)Tgc>Agc p.C386S COAD 4 153250925 153250925 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:153250925G>A c.1135C>T c.(1135-1137)Cat>Tat p.H379Y COAD 4 153251895 153251895 + Nonsense_Mutation SNP T T A TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr4:153251895T>A c.1111A>T c.(1111-1113)Aaa>Taa p.K371* COAD 4 153251905 153251905 + Silent SNP T T C TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R COAD 4 153251906 153251906 + Missense_Mutation SNP C C A TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr4:153251906C>A c.1100G>T c.(1099-1101)cGa>cTa p.R367L COAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COAD 4 153251991 153251991 + Nonsense_Mutation SNP T T A TCGA-AA-3982-01A-02W-0995-10 TCGA-AA-3982-10A-01W-0999-10 g.chr4:153251991T>A c.1015A>T c.(1015-1017)Aga>Tga p.R339* COAD 4 153253788 153253788 + Silent SNP A A G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COAD 4 153253788 153253788 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COAD 4 153253788 153253788 + Silent SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COAD 4 153253797 153253797 + Silent SNP T T C TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153253797T>C c.936A>G c.(934-936)agA>agG p.R312R COAD 4 153253799 153253799 + Missense_Mutation SNP T T C TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr4:153253799T>C c.934A>G c.(934-936)Aga>Gga p.R312G COAD 4 153253799 153253799 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153253799T>C c.934A>G c.(934-936)Aga>Gga p.R312G COAD 4 153253824 153253824 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q COAD 4 153253824 153253824 + Silent SNP T T C TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q COAD 4 153253839 153253839 + Silent SNP G G A TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr4:153253839G>A c.894C>T c.(892-894)ccC>ccT p.P298P COAD 4 153253853 153253853 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:153253853A>G c.880T>C c.(880-882)Tca>Cca p.S294P COAD 4 153253872 153253872 + Splice_Site SNP C C A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr4:153253872C>A c.e6-1 COAD 4 153253872 153253872 + Splice_Site SNP C C T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr4:153253872C>T c.e6-1 COAD 4 153258955 153258955 + Splice_Site SNP T T A TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr4:153258955T>A c.860A>T c.(859-861)gAg>gTg p.E287V COAD 4 153258970 153258970 + Nonsense_Mutation SNP G G T TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr4:153258970G>T c.845C>A c.(844-846)tCa>tAa p.S282* COAD 4 153258980 153258980 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr4:153258980C>A c.835G>T c.(835-837)Gac>Tac p.D279Y COAD 4 153258981 153258981 + Silent SNP T T C TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr4:153258981T>C c.834A>G c.(832-834)cgA>cgG p.R278R COAD 4 153258981 153258981 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153258981T>C c.834A>G c.(832-834)cgA>cgG p.R278R COAD 4 153259023 153259023 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153259023T>C c.792A>G c.(790-792)caA>caG p.Q264Q COAD 4 153259024 153259024 + Missense_Mutation SNP T T C TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr4:153259024T>C c.791A>G c.(790-792)cAa>cGa p.Q264R COAD 4 153259024 153259024 + Missense_Mutation SNP T T C TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr4:153259024T>C c.791A>G c.(790-792)cAa>cGa p.Q264R COAD 4 153268148 153268148 + Silent SNP T T C TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr4:153268148T>C c.660A>G c.(658-660)caA>caG p.Q220Q COAD 4 153268148 153268148 + Silent SNP T T C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr4:153268148T>C c.660A>G c.(658-660)caA>caG p.Q220Q COAD 4 153268222 153268222 + Splice_Site SNP T T A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:153268222T>A c.586A>T c.(586-588)Acc>Tcc p.T196S COAD 4 153271203 153271203 + Missense_Mutation SNP T T C TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr4:153271203T>C c.575A>G c.(574-576)gAa>gGa p.E192G COAD 4 153271203 153271203 + Missense_Mutation SNP T T G TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr4:153271203T>G c.575A>C c.(574-576)gAa>gCa p.E192A COAD 4 153271206 153271206 + Nonsense_Mutation SNP G G C TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr4:153271206G>C c.572C>G c.(571-573)tCa>tGa p.S191* COAD 4 153273739 153273739 + Intron DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr4:153273739delT COAD 4 153303407 153303407 + Intron SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:153303407A>G COAD 4 153332456 153332456 + Splice_Site SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153332456T>G c.500A>C c.(499-501)aAa>aCa p.K167T COAD 4 153332464 153332464 + Silent SNP T T C TCGA-AZ-6607-01A-11D-1835-10 TCGA-AZ-6607-11A-01D-1835-10 g.chr4:153332464T>C c.492A>G c.(490-492)aaA>aaG p.K164K COAD 4 153332488 153332488 + Missense_Mutation SNP T T A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr4:153332488T>A c.468A>T c.(466-468)caA>caT p.Q156H COAD 4 153332489 153332489 + Missense_Mutation SNP T T C TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr4:153332489T>C c.467A>G c.(466-468)cAa>cGa p.Q156R COAD 4 153332524 153332524 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:153332524C>T c.432G>A c.(430-432)acG>acA p.T144T COAD 4 153332617 153332617 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:153332617C>A c.339G>T c.(337-339)gaG>gaT p.E113D COAD 4 153332627 153332627 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr4:153332627T>C c.329A>G c.(328-330)gAg>gGg p.E110G COAD 4 153332662 153332662 + Silent SNP T T C TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q COAD 4 153332662 153332662 + Silent SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q COAD 4 153332663 153332663 + Missense_Mutation SNP T T C TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr4:153332663T>C c.293A>G c.(292-294)cAa>cGa p.Q98R COAD 4 153332663 153332663 + Missense_Mutation SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr4:153332663T>C c.293A>G c.(292-294)cAa>cGa p.Q98R COAD 4 153332679 153332679 + Nonsense_Mutation SNP C C A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:153332679C>A c.277G>T c.(277-279)Gga>Tga p.G93* COAD 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q COAD 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q COAD 4 153332916 153332916 + Nonsense_Mutation SNP G G A TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr4:153332916G>A c.40C>T c.(40-42)Cga>Tga p.R14* COAD 4 153332917 153332917 + Silent SNP T T C TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COAD 4 153332917 153332917 + Silent SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COAD 4 153332917 153332917 + Silent SNP T T C TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COAD 4 153332919 153332919 + Nonsense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr4:153332919G>A c.37C>T c.(37-39)Cga>Tga p.R13* COAD 4 153332923 153332923 + Missense_Mutation SNP T T G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr4:153332923T>G c.33A>C c.(31-33)aaA>aaC p.K11N COAD 4 153332923 153332923 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153332923T>C c.33A>G c.(31-33)aaA>aaG p.K11K COADREAD 4 153244078 153244078 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COADREAD 4 153244078 153244078 + Silent SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COADREAD 4 153244078 153244078 + Silent SNP T T C TCGA-D5-7000-01A-11D-1924-10 TCGA-D5-7000-10A-01D-1924-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COADREAD 4 153244078 153244078 + Silent SNP T T C TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E COADREAD 4 153244079 153244079 + Missense_Mutation SNP T T C TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153244079T>C c.2078A>G c.(2077-2079)gAa>gGa p.E693G COADREAD 4 153244079 153244079 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr4:153244079T>C c.2078A>G c.(2077-2079)gAa>gGa p.E693G COADREAD 4 153244090 153244090 + Silent SNP C C T TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr4:153244090C>T c.2067G>A c.(2065-2067)cgG>cgA p.R689R COADREAD 4 153244091 153244091 + Missense_Mutation SNP C C A TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr4:153244091C>A c.2066G>T c.(2065-2067)cGg>cTg p.R689L COADREAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COADREAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COADREAD 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-AA-3524-01A-02W-0831-10 TCGA-AA-3524-10A-01W-0831-10 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W COADREAD 4 153244136 153244136 + Missense_Mutation SNP C C A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr4:153244136C>A c.2021G>T c.(2020-2022)cGg>cTg p.R674L COADREAD 4 153244141 153244141 + Silent SNP C C T TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153244141C>T c.2016G>A c.(2014-2016)gtG>gtA p.V672V COADREAD 4 153244156 153244156 + Frame_Shift_Del DEL C C - TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153244156delC c.2001delG c.(1999-2001)gggfs p.G667fs COADREAD 4 153244184 153244184 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr4:153244184C>T c.1973G>A c.(1972-1974)cGa>cAa p.R658Q COADREAD 4 153244184 153244184 + Missense_Mutation SNP C C T TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153244184C>T c.1973G>A c.(1972-1974)cGa>cAa p.R658Q COADREAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COADREAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COADREAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COADREAD 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* COADREAD 4 153244204 153244204 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr4:153244204C>T c.1953G>A c.(1951-1953)ttG>ttA p.L651L COADREAD 4 153244206 153244206 + Silent SNP A A G TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr4:153244206A>G c.1951T>C c.(1951-1953)Ttg>Ctg p.L651L COADREAD 4 153244210 153244210 + Nonsense_Mutation SNP C C T TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr4:153244210C>T c.1947G>A c.(1945-1947)tgG>tgA p.W649* COADREAD 4 153244280 153244280 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr4:153244280G>T c.1877C>A c.(1876-1878)gCt>gAt p.A626D COADREAD 4 153245343 153245343 + Silent SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr4:153245343T>A c.1848A>T c.(1846-1848)acA>acT p.T616T COADREAD 4 153245393 153245393 + Missense_Mutation SNP C C A TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr4:153245393C>A c.1798G>T c.(1798-1800)Gat>Tat p.D600Y COADREAD 4 153245398 153245398 + Missense_Mutation SNP T T C TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr4:153245398T>C c.1793A>G c.(1792-1794)aAt>aGt p.N598S COADREAD 4 153245403 153245403 + Silent SNP A A T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr4:153245403A>T c.1788T>A c.(1786-1788)tcT>tcA p.S596S COADREAD 4 153245405 153245405 + Missense_Mutation SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr4:153245405A>G c.1786T>C c.(1786-1788)Tct>Cct p.S596P COADREAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COADREAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COADREAD 4 153245410 153245410 + Missense_Mutation SNP A A G TCGA-D5-7000-01A-11D-1924-10 TCGA-D5-7000-10A-01D-1924-10 g.chr4:153245410A>G c.1781T>C c.(1780-1782)cTt>cCt p.L594P COADREAD 4 153245445 153245445 + Silent SNP C C T TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr4:153245445C>T c.1746G>A c.(1744-1746)tcG>tcA p.S582S COADREAD 4 153245445 153245445 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153245445C>T c.1746G>A c.(1744-1746)tcG>tcA p.S582S COADREAD 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AA-3831-01A-01W-0900-09 TCGA-AA-3831-10A-01W-0900-09 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L COADREAD 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L COADREAD 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L COADREAD 4 153245446 153245446 + Nonsense_Mutation SNP G G T TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr4:153245446G>T c.1745C>A c.(1744-1746)tCg>tAg p.S582* COADREAD 4 153245447 153245447 + Missense_Mutation SNP A A T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153245447A>T c.1744T>A c.(1744-1746)Tcg>Acg p.S582T COADREAD 4 153245450 153245450 + Nonsense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr4:153245450G>A c.1741C>T c.(1741-1743)Cag>Tag p.Q581* COADREAD 4 153245453 153245453 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153245453G>A c.1738C>T c.(1738-1740)Cac>Tac p.H580Y COADREAD 4 153245461 153245461 + Missense_Mutation SNP A A G TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr4:153245461A>G c.1730T>C c.(1729-1731)tTa>tCa p.L577S COADREAD 4 153247167 153247167 + Silent SNP A A G TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr4:153247167A>G c.1635T>C c.(1633-1635)taT>taC p.Y545Y COADREAD 4 153247167 153247167 + Silent SNP A A G TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr4:153247167A>G c.1635T>C c.(1633-1635)taT>taC p.Y545Y COADREAD 4 153247168 153247168 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr4:153247168T>C c.1634A>G c.(1633-1635)tAt>tGt p.Y545C COADREAD 4 153247169 153247169 + Missense_Mutation SNP A A G TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr4:153247169A>G c.1633T>C c.(1633-1635)Tat>Cat p.Y545H COADREAD 4 153247173 153247173 + Silent SNP T T C TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153247173T>C c.1629A>G c.(1627-1629)agA>agG p.R543R COADREAD 4 153247183 153247183 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153247183T>C c.1619A>G c.(1618-1620)cAt>cGt p.H540R COADREAD 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A COADREAD 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A COADREAD 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A COADREAD 4 153247221 153247221 + Silent SNP A A G TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153247221A>G c.1581T>C c.(1579-1581)gaT>gaC p.D527D COADREAD 4 153247222 153247222 + Missense_Mutation SNP T T C TCGA-A6-5656-01A-21D-1835-10 TCGA-A6-5656-10A-01D-1835-10 g.chr4:153247222T>C c.1580A>G c.(1579-1581)gAt>gGt p.D527G COADREAD 4 153247223 153247223 + Missense_Mutation SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr4:153247223C>T c.1579G>A c.(1579-1581)Gat>Aat p.D527N COADREAD 4 153247244 153247244 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153247244C>A c.1558G>T c.(1558-1560)Gat>Tat p.D520Y COADREAD 4 153247244 153247244 + Missense_Mutation SNP C C T TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr4:153247244C>T c.1558G>A c.(1558-1560)Gat>Aat p.D520N COADREAD 4 153247288 153247288 + Missense_Mutation SNP C C A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153247288C>A c.1514G>T c.(1513-1515)cGc>cTc p.R505L COADREAD 4 153247288 153247288 + Missense_Mutation SNP C C T TCGA-AA-A024-01A-02W-A00E-09 TCGA-AA-A024-10A-01W-A00E-09 g.chr4:153247288C>T c.1514G>A c.(1513-1515)cGc>cAc p.R505H COADREAD 4 153247288 153247288 + Missense_Mutation SNP C C T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr4:153247288C>T c.1514G>A c.(1513-1515)cGc>cAc p.R505H COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-A6-3807-01A-01W-0995-10 TCGA-A6-3807-11A-01W-0995-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AA-3560-01A-01W-0831-10 TCGA-AA-3560-10A-01W-0831-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AG-3885-01A-01W-0899-10 TCGA-AG-3885-10A-01W-0901-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-A6-2677-01A-01W-0831-10 TCGA-A6-2677-10A-01W-0831-10 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G COADREAD 4 153247289 153247289 + Missense_Mutation SNP G G T TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chr4:153247289G>T c.1513C>A c.(1513-1515)Cgc>Agc p.R505S COADREAD 4 153247291 153247291 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr4:153247291A>G c.1511T>C c.(1510-1512)gTc>gCc p.V504A COADREAD 4 153247291 153247291 + Missense_Mutation SNP A A G TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr4:153247291A>G c.1511T>C c.(1510-1512)gTc>gCc p.V504A COADREAD 4 153247318 153247318 + Missense_Mutation SNP T T G TCGA-AG-3600-01A-01W-0833-10 TCGA-AG-3600-10A-01W-0833-10 g.chr4:153247318T>G c.1484A>C c.(1483-1485)cAt>cCt p.H495P COADREAD 4 153247327 153247327 + Frame_Shift_Del DEL T T - TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr4:153247327delT c.1475delA c.(1474-1476)cagfs p.Q492fs COADREAD 4 153247345 153247345 + Missense_Mutation SNP C C A TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153247345C>A c.1457G>T c.(1456-1458)tGg>tTg p.W486L COADREAD 4 153247351 153247351 + Missense_Mutation SNP C C A TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr4:153247351C>A c.1451G>T c.(1450-1452)aGg>aTg p.R484M COADREAD 4 153247363 153247363 + Missense_Mutation SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153247363T>C c.1439A>G c.(1438-1440)gAt>gGt p.D480G COADREAD 4 153247363 153247363 + Missense_Mutation SNP T T C TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr4:153247363T>C c.1439A>G c.(1438-1440)gAt>gGt p.D480G COADREAD 4 153247365 153247365 + Silent SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr4:153247365T>C c.1437A>G c.(1435-1437)cgA>cgG p.R479R COADREAD 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q COADREAD 4 153247367 153247367 + Missense_Mutation SNP G G C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr4:153247367G>C c.1435C>G c.(1435-1437)Cga>Gga p.R479G COADREAD 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* COADREAD 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-A6-6137-01A-11D-1771-10 TCGA-A6-6137-10A-01D-1806-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* COADREAD 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* COADREAD 4 153247374 153247374 + Missense_Mutation SNP G G T TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr4:153247374G>T c.1428C>A c.(1426-1428)agC>agA p.S476R COADREAD 4 153249360 153249361 + Splice_Site INS - - T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153249360_153249361insT c.1417_1418insA c.(1417-1419)aga>aAga p.R473fs COADREAD 4 153249361 153249361 + Splice_Site DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr4:153249361delT c.1417delA c.(1417-1419)aga>ga p.R473fs COADREAD 4 153249369 153249369 + Missense_Mutation SNP T T C TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr4:153249369T>C c.1409A>G c.(1408-1410)cAt>cGt p.H470R COADREAD 4 153249383 153249383 + Silent SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COADREAD 4 153249383 153249383 + Silent SNP A A G TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COADREAD 4 153249383 153249383 + Silent SNP A A G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COADREAD 4 153249383 153249383 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr4:153249384C>G c.1394G>C c.(1393-1395)cGt>cCt p.R465P COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3681-01A-01W-0900-09 TCGA-AA-3681-10A-01W-0900-09 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-3852-01A-01W-0900-09 TCGA-AA-3852-10A-01W-0900-09 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AG-3608-01A-01W-0833-10 TCGA-AG-3608-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AG-3881-01A-01W-0899-10 TCGA-AG-3881-10A-01W-0901-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AA-3848-01A-01W-0900-09 TCGA-AA-3848-10A-01W-0900-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AG-3898-01A-01W-1073-09 TCGA-AG-3898-10A-01W-1073-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C COADREAD 4 153249385 153249385 + Missense_Mutation SNP G G T TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr4:153249385G>T c.1393C>A c.(1393-1395)Cgt>Agt p.R465S COADREAD 4 153249400 153249400 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr4:153249400G>A c.1378C>T c.(1378-1380)Cat>Tat p.H460Y COADREAD 4 153249440 153249440 + Nonsense_Mutation SNP C C T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr4:153249440C>T c.1338G>A c.(1336-1338)tgG>tgA p.W446* COADREAD 4 153249440 153249440 + Nonsense_Mutation SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153249440C>T c.1338G>A c.(1336-1338)tgG>tgA p.W446* COADREAD 4 153249441 153249441 + Nonsense_Mutation SNP C C T TCGA-F4-6704-01A-11D-1835-10 TCGA-F4-6704-11A-01D-1835-10 g.chr4:153249441C>T c.1337G>A c.(1336-1338)tGg>tAg p.W446* COADREAD 4 153249442 153249442 + Missense_Mutation SNP A A G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153249442A>G c.1336T>C c.(1336-1338)Tgg>Cgg p.W446R COADREAD 4 153249451 153249451 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153249451G>A c.1327C>T c.(1327-1329)Ctc>Ttc p.L443F COADREAD 4 153249456 153249456 + Missense_Mutation SNP C C A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr4:153249456C>A c.1322G>T c.(1321-1323)cGg>cTg p.R441L COADREAD 4 153249456 153249456 + Missense_Mutation SNP C C A TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr4:153249456C>A c.1322G>T c.(1321-1323)cGg>cTg p.R441L COADREAD 4 153249457 153249457 + Missense_Mutation SNP G G A TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr4:153249457G>A c.1321C>T c.(1321-1323)Cgg>Tgg p.R441W COADREAD 4 153249457 153249457 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr4:153249457G>A c.1321C>T c.(1321-1323)Cgg>Tgg p.R441W COADREAD 4 153249457 153249457 + Silent SNP G G T TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr4:153249457G>T c.1321C>A c.(1321-1323)Cgg>Agg p.R441R COADREAD 4 153249457 153249457 + Silent SNP G G T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr4:153249457G>T c.1321C>A c.(1321-1323)Cgg>Agg p.R441R COADREAD 4 153249460 153249460 + Missense_Mutation SNP C C A TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr4:153249460C>A c.1318G>T c.(1318-1320)Gat>Tat p.D440Y COADREAD 4 153249465 153249465 + Missense_Mutation SNP G G A TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr4:153249465G>A c.1313C>T c.(1312-1314)tCt>tTt p.S438F COADREAD 4 153249465 153249465 + Missense_Mutation SNP G G T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr4:153249465G>T c.1313C>A c.(1312-1314)tCt>tAt p.S438Y COADREAD 4 153249466 153249466 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153249466A>G c.1312T>C c.(1312-1314)Tct>Cct p.S438P COADREAD 4 153249469 153249469 + Missense_Mutation SNP C C T TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr4:153249469C>T c.1309G>A c.(1309-1311)Gga>Aga p.G437R COADREAD 4 153249509 153249509 + Silent SNP T T A TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr4:153249509T>A c.1269A>T c.(1267-1269)ggA>ggT p.G423G COADREAD 4 153249509 153249509 + Silent SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr4:153249509T>C c.1269A>G c.(1267-1269)ggA>ggG p.G423G COADREAD 4 153249510 153249510 + Missense_Mutation SNP C C A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr4:153249510C>A c.1268G>T c.(1267-1269)gGa>gTa p.G423V COADREAD 4 153249518 153249518 + Silent SNP A A G TCGA-DM-A1D8-01A-11D-A152-10 TCGA-DM-A1D8-10A-01D-A152-10 g.chr4:153249518A>G c.1260T>C c.(1258-1260)caT>caC p.H420H COADREAD 4 153249518 153249519 + Frame_Shift_Ins INS - - TGTCCCAC TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr4:153249518_153249519insTGTCCCAC c.1259_1260insGTGGGACA c.(1258-1260)catfs p.H420fs COADREAD 4 153249519 153249519 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr4:153249519T>C c.1259A>G c.(1258-1260)cAt>cGt p.H420R COADREAD 4 153249519 153249519 + Missense_Mutation SNP T T C TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr4:153249519T>C c.1259A>G c.(1258-1260)cAt>cGt p.H420R COADREAD 4 153250848 153250848 + Frame_Shift_Del DEL T T - TCGA-DM-A0XD-01A-12D-A152-10 TCGA-DM-A0XD-10A-01D-A152-10 g.chr4:153250848delT c.1212delA c.(1210-1212)aaafs p.K404fs COADREAD 4 153250856 153250858 + In_Frame_Del DEL TGT TGT - TCGA-AG-3594-01A-02W-0831-10 TCGA-AG-3594-10A-01W-0831-10 g.chr4:153250856_153250858delTGT c.1202_1204delACA c.(1201-1206)aacact>act p.N401del COADREAD 4 153250882 153250882 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153250882C>T c.1178G>A c.(1177-1179)cGa>cAa p.R393Q COADREAD 4 153250904 153250904 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:153250904A>T c.1156T>A c.(1156-1158)Tgc>Agc p.C386S COADREAD 4 153250925 153250925 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:153250925G>A c.1135C>T c.(1135-1137)Cat>Tat p.H379Y COADREAD 4 153251895 153251895 + Nonsense_Mutation SNP T T A TCGA-AD-6548-01A-11D-1835-10 TCGA-AD-6548-10A-01D-1835-10 g.chr4:153251895T>A c.1111A>T c.(1111-1113)Aaa>Taa p.K371* COADREAD 4 153251901 153251901 + Nonsense_Mutation SNP C C A TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr4:153251901C>A c.1105G>T c.(1105-1107)Gaa>Taa p.E369* COADREAD 4 153251905 153251905 + Silent SNP T T C TCGA-AH-6547-01A-11D-1826-10 TCGA-AH-6547-11A-02D-1826-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R COADREAD 4 153251905 153251905 + Silent SNP T T C TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R COADREAD 4 153251905 153251905 + Silent SNP T T C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R COADREAD 4 153251906 153251906 + Missense_Mutation SNP C C A TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr4:153251906C>A c.1100G>T c.(1099-1101)cGa>cTa p.R367L COADREAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COADREAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COADREAD 4 153251907 153251907 + Nonsense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr4:153251907G>A c.1099C>T c.(1099-1101)Cga>Tga p.R367* COADREAD 4 153251991 153251991 + Nonsense_Mutation SNP T T A TCGA-AA-3982-01A-02W-0995-10 TCGA-AA-3982-10A-01W-0999-10 g.chr4:153251991T>A c.1015A>T c.(1015-1017)Aga>Tga p.R339* COADREAD 4 153253788 153253788 + Silent SNP A A G TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COADREAD 4 153253788 153253788 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COADREAD 4 153253788 153253788 + Silent SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr4:153253788A>G c.945T>C c.(943-945)gcT>gcC p.A315A COADREAD 4 153253790 153253790 + Missense_Mutation SNP C C T TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr4:153253790C>T c.943G>A c.(943-945)Gct>Act p.A315T COADREAD 4 153253797 153253797 + Silent SNP T T C TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr4:153253797T>C c.936A>G c.(934-936)agA>agG p.R312R COADREAD 4 153253799 153253799 + Missense_Mutation SNP T T C TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr4:153253799T>C c.934A>G c.(934-936)Aga>Gga p.R312G COADREAD 4 153253799 153253799 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr4:153253799T>C c.934A>G c.(934-936)Aga>Gga p.R312G COADREAD 4 153253824 153253824 + Silent SNP T T C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q COADREAD 4 153253824 153253824 + Silent SNP T T C TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q COADREAD 4 153253824 153253824 + Silent SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q COADREAD 4 153253839 153253839 + Silent SNP G G A TCGA-G4-6625-01A-21D-1771-10 TCGA-G4-6625-11A-01D-1771-10 g.chr4:153253839G>A c.894C>T c.(892-894)ccC>ccT p.P298P COADREAD 4 153253853 153253853 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr4:153253853A>G c.880T>C c.(880-882)Tca>Cca p.S294P COADREAD 4 153253872 153253872 + Splice_Site SNP C C A TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr4:153253872C>A c.e6-1 COADREAD 4 153253872 153253872 + Splice_Site SNP C C T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr4:153253872C>T c.e6-1 COADREAD 4 153258955 153258955 + Splice_Site SNP T T A TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr4:153258955T>A c.860A>T c.(859-861)gAg>gTg p.E287V COADREAD 4 153258969 153258969 + Silent SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr4:153258969T>C c.846A>G c.(844-846)tcA>tcG p.S282S COADREAD 4 153258970 153258970 + Nonsense_Mutation SNP G G T TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr4:153258970G>T c.845C>A c.(844-846)tCa>tAa p.S282* COADREAD 4 153258971 153258971 + Missense_Mutation SNP A A T TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr4:153258971A>T c.844T>A c.(844-846)Tca>Aca p.S282T COADREAD 4 153258980 153258980 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr4:153258980C>A c.835G>T c.(835-837)Gac>Tac p.D279Y COADREAD 4 153258981 153258981 + Silent SNP T T C TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr4:153258981T>C c.834A>G c.(832-834)cgA>cgG p.R278R COADREAD 4 153258981 153258981 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153258981T>C c.834A>G c.(832-834)cgA>cgG p.R278R COADREAD 4 153258991 153258995 + Frame_Shift_Del DEL TGGGG TGGGG - TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr4:153258991_153258995delTGGGG c.820_824delCCCCA c.(820-825)ccccagfs p.PQ274fs COADREAD 4 153259023 153259023 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153259023T>C c.792A>G c.(790-792)caA>caG p.Q264Q COADREAD 4 153259024 153259024 + Missense_Mutation SNP T T C TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr4:153259024T>C c.791A>G c.(790-792)cAa>cGa p.Q264R COADREAD 4 153259024 153259024 + Missense_Mutation SNP T T C TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr4:153259024T>C c.791A>G c.(790-792)cAa>cGa p.Q264R COADREAD 4 153268093 153268093 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153268093T>G c.715A>C c.(715-717)Aaa>Caa p.K239Q COADREAD 4 153268148 153268148 + Silent SNP T T C TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr4:153268148T>C c.660A>G c.(658-660)caA>caG p.Q220Q COADREAD 4 153268148 153268148 + Silent SNP T T C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr4:153268148T>C c.660A>G c.(658-660)caA>caG p.Q220Q COADREAD 4 153268222 153268222 + Splice_Site SNP T T A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr4:153268222T>A c.586A>T c.(586-588)Acc>Tcc p.T196S COADREAD 4 153271203 153271203 + Missense_Mutation SNP T T C TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr4:153271203T>C c.575A>G c.(574-576)gAa>gGa p.E192G COADREAD 4 153271203 153271203 + Missense_Mutation SNP T T G TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr4:153271203T>G c.575A>C c.(574-576)gAa>gCa p.E192A COADREAD 4 153271206 153271206 + Nonsense_Mutation SNP G G C TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr4:153271206G>C c.572C>G c.(571-573)tCa>tGa p.S191* COADREAD 4 153271206 153271206 + Nonsense_Mutation SNP G G C TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr4:153271206G>C c.572C>G c.(571-573)tCa>tGa p.S191* COADREAD 4 153271242 153271242 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153271242C>T c.536G>A c.(535-537)cGc>cAc p.R179H COADREAD 4 153273739 153273739 + Intron DEL T T - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr4:153273739delT COADREAD 4 153273871 153273871 + Intron SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153273871C>T COADREAD 4 153303407 153303407 + Intron SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:153303407A>G COADREAD 4 153332456 153332456 + Splice_Site SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153332456T>G c.500A>C c.(499-501)aAa>aCa p.K167T COADREAD 4 153332464 153332464 + Silent SNP T T C TCGA-AZ-6607-01A-11D-1835-10 TCGA-AZ-6607-11A-01D-1835-10 g.chr4:153332464T>C c.492A>G c.(490-492)aaA>aaG p.K164K COADREAD 4 153332488 153332488 + Missense_Mutation SNP T T A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr4:153332488T>A c.468A>T c.(466-468)caA>caT p.Q156H COADREAD 4 153332489 153332489 + Missense_Mutation SNP T T C TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr4:153332489T>C c.467A>G c.(466-468)cAa>cGa p.Q156R COADREAD 4 153332524 153332524 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:153332524C>T c.432G>A c.(430-432)acG>acA p.T144T COADREAD 4 153332617 153332617 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr4:153332617C>A c.339G>T c.(337-339)gaG>gaT p.E113D COADREAD 4 153332627 153332627 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr4:153332627T>C c.329A>G c.(328-330)gAg>gGg p.E110G COADREAD 4 153332662 153332662 + Silent SNP T T C TCGA-A6-6782-01A-11D-1835-10 TCGA-A6-6782-10A-01D-1835-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q COADREAD 4 153332662 153332662 + Silent SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q COADREAD 4 153332662 153332662 + Silent SNP T T C TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q COADREAD 4 153332663 153332663 + Missense_Mutation SNP T T C TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr4:153332663T>C c.293A>G c.(292-294)cAa>cGa p.Q98R COADREAD 4 153332663 153332663 + Missense_Mutation SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr4:153332663T>C c.293A>G c.(292-294)cAa>cGa p.Q98R COADREAD 4 153332679 153332679 + Nonsense_Mutation SNP C C A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:153332679C>A c.277G>T c.(277-279)Gga>Tga p.G93* COADREAD 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q COADREAD 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q COADREAD 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q COADREAD 4 153332916 153332916 + Nonsense_Mutation SNP G G A TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr4:153332916G>A c.40C>T c.(40-42)Cga>Tga p.R14* COADREAD 4 153332917 153332917 + Silent SNP T T C TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COADREAD 4 153332917 153332917 + Silent SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COADREAD 4 153332917 153332917 + Silent SNP T T C TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COADREAD 4 153332917 153332917 + Silent SNP T T C TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R COADREAD 4 153332919 153332919 + Nonsense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr4:153332919G>A c.37C>T c.(37-39)Cga>Tga p.R13* COADREAD 4 153332919 153332919 + Nonsense_Mutation SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153332919G>A c.37C>T c.(37-39)Cga>Tga p.R13* COADREAD 4 153332923 153332923 + Missense_Mutation SNP T T G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr4:153332923T>G c.33A>C c.(31-33)aaA>aaC p.K11N COADREAD 4 153332923 153332923 + Silent SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr4:153332923T>C c.33A>G c.(31-33)aaA>aaG p.K11K ESCA 4 153244156 153244156 + Frame_Shift_Del DEL C C - TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr4:153244156delC c.2001delG c.(1999-2001)gggfs p.G667fs ESCA 4 153244238 153244238 + Frame_Shift_Del DEL C C - TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr4:153244238delC c.1919delG c.(1918-1920)agcfs p.S641fs ESCA 4 153245464 153245464 + Missense_Mutation SNP G G A TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr4:153245464G>A c.1727C>T c.(1726-1728)aCg>aTg p.T576M ESCA 4 153247174 153247175 + Frame_Shift_Ins INS - - TATT TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr4:153247174_153247175insTATT c.1627_1628insAATA c.(1627-1629)agafs p.R543fs ESCA 4 153247195 153247195 + Missense_Mutation SNP G G C TCGA-R6-A6L4-01A-11D-A31U-09 TCGA-R6-A6L4-10A-01D-A31U-09 g.chr4:153247195G>C c.1607C>G c.(1606-1608)aCg>aGg p.T536R ESCA 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C ESCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-IG-A3YB-01A-11D-A247-09 TCGA-IG-A3YB-10A-01D-A247-09 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G ESCA 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G ESCA 4 153249360 153249361 + Splice_Site INS - - T TCGA-R6-A8W5-01B-11D-A37C-09 TCGA-R6-A8W5-10A-01D-A37F-09 g.chr4:153249360_153249361insT c.1417_1418insA c.(1417-1419)aga>aAga p.R473fs ESCA 4 153250883 153250883 + Nonsense_Mutation SNP G G A TCGA-XP-A8T7-01A-11D-A36J-09 TCGA-XP-A8T7-10A-01D-A36M-09 g.chr4:153250883G>A c.1177C>T c.(1177-1179)Cga>Tga p.R393* ESCA 4 153251886 153251886 + Missense_Mutation SNP T T G TCGA-IG-A7DP-01A-31D-A33E-09 TCGA-IG-A7DP-10A-01D-A33H-09 g.chr4:153251886T>G c.1120A>C c.(1120-1122)Aag>Cag p.K374Q ESCA 4 153252003 153252003 + Missense_Mutation SNP G G A TCGA-L5-A8NN-01A-11D-A37C-09 TCGA-L5-A8NN-11A-11D-A37F-09 g.chr4:153252003G>A c.1003C>T c.(1003-1005)Cac>Tac p.H335Y ESCA 4 153253853 153253853 + Missense_Mutation SNP A A G TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr4:153253853A>G c.880T>C c.(880-882)Tca>Cca p.S294P ESCA 4 153332739 153332739 + Nonsense_Mutation SNP G G A TCGA-2H-A9GN-01A-11D-A37C-09 TCGA-2H-A9GN-11A-11D-A37F-09 g.chr4:153332739G>A c.217C>T c.(217-219)Cag>Tag p.Q73* GBM 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* GBMLGG 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-QH-A6CS-01A-11D-A31L-08 TCGA-QH-A6CS-10A-01D-A31J-08 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W GBMLGG 4 153244137 153244137 + Missense_Mutation SNP G G A TCGA-HT-A618-01A-11D-A29Q-08 TCGA-HT-A618-10A-01D-A29Q-08 g.chr4:153244137G>A c.2020C>T c.(2020-2022)Cgg>Tgg p.R674W GBMLGG 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* GBMLGG 4 153244280 153244280 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:153244280G>T c.1877C>A c.(1876-1878)gCt>gAt p.A626D GBMLGG 4 153251912 153251912 + Missense_Mutation SNP C C G TCGA-S9-A6TS-01A-12D-A33T-08 TCGA-S9-A6TS-10A-01D-A33W-08 g.chr4:153251912C>G c.1094G>C c.(1093-1095)tGg>tCg p.W365S HNSC 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-MT-A67A-01A-11D-A30E-08 TCGA-MT-A67A-10A-01D-A30H-08 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* HNSC 4 153245424 153245424 + Silent SNP G G A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr4:153245424G>A c.1767C>T c.(1765-1767)ctC>ctT p.L589L HNSC 4 153247161 153247162 + Frame_Shift_Ins INS - - A TCGA-MT-A67A-01A-11D-A30E-08 TCGA-MT-A67A-10A-01D-A30H-08 g.chr4:153247161_153247162insA c.1640_1641insT c.(1639-1641)ttafs p.L547fs HNSC 4 153247165 153247165 + Nonsense_Mutation SNP G G C TCGA-UF-A7J9-01A-12D-A34J-08 TCGA-UF-A7J9-10A-01D-A34M-08 g.chr4:153247165G>C c.1637C>G c.(1636-1638)tCa>tGa p.S546* HNSC 4 153247168 153247168 + Missense_Mutation SNP T T C TCGA-CV-A45R-01A-11D-A24D-08 TCGA-CV-A45R-10A-01D-A24F-08 g.chr4:153247168T>C c.1634A>G c.(1633-1635)tAt>tGt p.Y545C HNSC 4 153247175 153247175 + Missense_Mutation SNP T T C TCGA-CN-5366-01A-01D-1434-08 TCGA-CN-5366-10A-01D-1434-08 g.chr4:153247175T>C c.1627A>G c.(1627-1629)Aga>Gga p.R543G HNSC 4 153247175 153247175 + Missense_Mutation SNP T T C TCGA-CQ-A4CE-01A-11D-A25Y-08 TCGA-CQ-A4CE-10A-01D-A25Y-08 g.chr4:153247175T>C c.1627A>G c.(1627-1629)Aga>Gga p.R543G HNSC 4 153247226 153247226 + Missense_Mutation SNP A A G TCGA-CR-7379-01A-11D-2012-08 TCGA-CR-7379-10A-01D-2013-08 g.chr4:153247226A>G c.1576T>C c.(1576-1578)Tgg>Cgg p.W526R HNSC 4 153247228 153247228 + Missense_Mutation SNP A A T TCGA-CN-6992-01A-11D-1912-08 TCGA-CN-6992-10A-01D-1912-08 g.chr4:153247228A>T c.1574T>A c.(1573-1575)gTg>gAg p.V525E HNSC 4 153247244 153247244 + Missense_Mutation SNP C C G TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr4:153247244C>G c.1558G>C c.(1558-1560)Gat>Cat p.D520H HNSC 4 153247255 153247255 + Missense_Mutation SNP C C T TCGA-CQ-6221-01A-11D-2078-08 TCGA-CQ-6221-10A-01D-2078-08 g.chr4:153247255C>T c.1547G>A c.(1546-1548)aGt>aAt p.S516N HNSC 4 153247288 153247288 + Missense_Mutation SNP C C A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr4:153247288C>A c.1514G>T c.(1513-1515)cGc>cTc p.R505L HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-BB-4228-01A-01D-1434-08 TCGA-BB-4228-10A-01D-1434-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-CN-A6V7-01A-12D-A34J-08 TCGA-CN-A6V7-10A-01D-A34M-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-CV-6436-01A-11D-1683-08 TCGA-CV-6436-11A-01D-1683-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-CV-A45V-01A-21D-A25D-08 TCGA-CV-A45V-10A-01D-A25E-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G HNSC 4 153247297 153247297 + Missense_Mutation SNP G G A TCGA-BA-6868-01B-12D-1912-08 TCGA-BA-6868-10A-01D-1912-08 g.chr4:153247297G>A c.1505C>T c.(1504-1506)gCa>gTa p.A502V HNSC 4 153247311 153247311 + Silent SNP C C T TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr4:153247311C>T c.1491G>A c.(1489-1491)ttG>ttA p.L497L HNSC 4 153247366 153247366 + Missense_Mutation SNP C C A TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr4:153247366C>A c.1436G>T c.(1435-1437)cGa>cTa p.R479L HNSC 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-CQ-A4CG-01A-11D-A25Y-08 TCGA-CQ-A4CG-10A-01D-A25Y-08 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q HNSC 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q HNSC 4 153247377 153247379 + In_Frame_Del DEL AAC AAC - TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chr4:153247377_153247379delAAC c.1423_1425delGTT c.(1423-1425)gttdel p.V475del HNSC 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-BA-A6DF-01A-11D-A30E-08 TCGA-BA-A6DF-10A-01D-A30H-08 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C HNSC 4 153249385 153249385 + Missense_Mutation SNP G G C TCGA-QK-A6II-01A-11D-A31L-08 TCGA-QK-A6II-10A-01D-A31J-08 g.chr4:153249385G>C c.1393C>G c.(1393-1395)Cgt>Ggt p.R465G HNSC 4 153249401 153249401 + Silent SNP C C T TCGA-CR-6480-01A-11D-1870-08 TCGA-CR-6480-10A-01D-1870-08 g.chr4:153249401C>T c.1377G>A c.(1375-1377)ggG>ggA p.G459G HNSC 4 153249510 153249510 + Missense_Mutation SNP C C G TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr4:153249510C>G c.1268G>C c.(1267-1269)gGa>gCa p.G423A HNSC 4 153249517 153249526 + Frame_Shift_Del DEL TATGTCCCAC TATGTCCCAC - TCGA-F7-A622-01A-11D-A28R-08 TCGA-F7-A622-10A-01D-A28U-08 g.chr4:153249517_153249526delTATGTCCCAC c.1252_1261delGTGGGACATA c.(1252-1263)gtgggacatacafs p.VGHT418fs HNSC 4 153249524 153249524 + Silent SNP C C A TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr4:153249524C>A c.1254G>T c.(1252-1254)gtG>gtT p.V418V HNSC 4 153250883 153250883 + Nonsense_Mutation SNP G G A TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr4:153250883G>A c.1177C>T c.(1177-1179)Cga>Tga p.R393* HNSC 4 153250891 153250910 + Frame_Shift_Del DEL CAAAACTGTAAGCATGTGAT CAAAACTGTAAGCATGTGAT - TCGA-CV-A6JY-01A-11D-A31L-08 TCGA-CV-A6JY-10A-01D-A31J-08 g.chr4:153250891_153250910delCAAAACTGTAAGCATGTGAT c.1150_1169delATCACATGCTTACAGTTTTG c.(1150-1170)atcacatgcttacagttttgtfs p.ITCLQFC384fs HNSC 4 153251878 153251886 + Splice_Site DEL AGTTACCTT AGTTACCTT - TCGA-CV-7263-01A-11D-2012-08 TCGA-CV-7263-10A-01D-2013-08 g.chr4:153251878_153251886delAGTTACCTT c.1120_1123delAAGGTAACT c.(1120-1125)aaggta>ta p.KV374del HNSC 4 153253749 153253750 + Splice_Site INS - - T TCGA-BB-8601-01A-11D-2394-08 TCGA-BB-8601-10A-01D-2394-08 g.chr4:153253749_153253750insT c.983_984insA c.(982-984)gag>gaAg p.E328fs HNSC 4 153259045 153259046 + Frame_Shift_Ins INS - - TGAGT TCGA-CR-7379-01A-11D-2012-08 TCGA-CR-7379-10A-01D-2013-08 g.chr4:153259045_153259046insTGAGT c.769_770insACTCA c.(769-771)attfs p.I257fs HNSC 4 153271277 153271277 + Splice_Site SNP C C G TCGA-P3-A6T7-01A-11D-A34J-08 TCGA-P3-A6T7-10A-01D-A34M-08 g.chr4:153271277C>G c.e3-1 HNSC 4 153332540 153332558 + Frame_Shift_Del DEL TGTGTATGTTCATCTTCTC TGTGTATGTTCATCTTCTC - TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chr4:153332540_153332558delTGTGTATGTTCATCTTCTC c.398_416delGAGAAGATGAACATACACA c.(397-417)agagaagatgaacatacacatfs p.REDEHTH133fs HNSC 4 153332853 153332853 + Missense_Mutation SNP G G A TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr4:153332853G>A c.103C>T c.(103-105)Cgt>Tgt p.R35C HNSC 4 153332882 153332882 + Nonsense_Mutation SNP G G C TCGA-CN-A498-01A-11D-A24D-08 TCGA-CN-A498-10A-01D-A24F-08 g.chr4:153332882G>C c.74C>G c.(73-75)tCa>tGa p.S25* KICH 4 153247276 153247276 + Missense_Mutation SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr4:153247276T>C c.1526A>G c.(1525-1527)tAt>tGt p.Y509C KICH 4 153332484 153332484 + Missense_Mutation SNP A A G TCGA-KN-8433-01A-11D-2310-10 TCGA-KN-8433-11A-01D-2311-10 g.chr4:153332484A>G c.472T>C c.(472-474)Tcc>Ccc p.S158P KIPAN 4 153244135 153244135 + Silent SNP C C G TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr4:153244135C>G c.2022G>C c.(2020-2022)cgG>cgC p.R674R KIPAN 4 153247276 153247276 + Missense_Mutation SNP T T C TCGA-KO-8405-01A-11D-2310-10 TCGA-KO-8405-11A-01D-2311-10 g.chr4:153247276T>C c.1526A>G c.(1525-1527)tAt>tGt p.Y509C KIPAN 4 153250883 153250883 + Frame_Shift_Del DEL G G - TCGA-MH-A561-01A-11D-A26P-10 TCGA-MH-A561-10A-01D-A26P-10 g.chr4:153250883delG c.1177delC c.(1177-1179)cgafs p.R393fs KIPAN 4 153273874 153273874 + Intron SNP G G A TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr4:153273874G>A KIPAN 4 153332484 153332484 + Missense_Mutation SNP A A G TCGA-KN-8433-01A-11D-2310-10 TCGA-KN-8433-11A-01D-2311-10 g.chr4:153332484A>G c.472T>C c.(472-474)Tcc>Ccc p.S158P KIPAN 4 153332528 153332528 + Missense_Mutation SNP A A T TCGA-B0-5102-01A-01D-1421-08 TCGA-B0-5102-11A-01D-1421-08 g.chr4:153332528A>T c.428T>A c.(427-429)gTc>gAc p.V143D KIRC 4 153244135 153244135 + Silent SNP C C G TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr4:153244135C>G c.2022G>C c.(2020-2022)cgG>cgC p.R674R KIRC 4 153332528 153332528 + Missense_Mutation SNP A A T TCGA-B0-5102-01A-01D-1421-08 TCGA-B0-5102-11A-01D-1421-08 g.chr4:153332528A>T c.428T>A c.(427-429)gTc>gAc p.V143D KIRP 4 153250883 153250883 + Frame_Shift_Del DEL G G - TCGA-MH-A561-01A-11D-A26P-10 TCGA-MH-A561-10A-01D-A26P-10 g.chr4:153250883delG c.1177delC c.(1177-1179)cgafs p.R393fs KIRP 4 153273874 153273874 + Intron SNP G G A TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr4:153273874G>A LGG 4 153244092 153244092 + Missense_Mutation SNP G G A TCGA-QH-A6CS-01A-11D-A31L-08 TCGA-QH-A6CS-10A-01D-A31J-08 g.chr4:153244092G>A c.2065C>T c.(2065-2067)Cgg>Tgg p.R689W LGG 4 153244137 153244137 + Missense_Mutation SNP G G A TCGA-HT-A618-01A-11D-A29Q-08 TCGA-HT-A618-10A-01D-A29Q-08 g.chr4:153244137G>A c.2020C>T c.(2020-2022)Cgg>Tgg p.R674W LGG 4 153244280 153244280 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:153244280G>T c.1877C>A c.(1876-1878)gCt>gAt p.A626D LGG 4 153251912 153251912 + Missense_Mutation SNP C C G TCGA-S9-A6TS-01A-12D-A33T-08 TCGA-S9-A6TS-10A-01D-A33W-08 g.chr4:153251912C>G c.1094G>C c.(1093-1095)tGg>tCg p.W365S LIHC 4 153244121 153244121 + Missense_Mutation SNP T T C TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr4:153244121T>C c.2036A>G c.(2035-2037)aAc>aGc p.N679S LIHC 4 153245454 153245454 + Silent SNP C C T TCGA-ZS-A9CE-01A-11D-A36X-10 TCGA-ZS-A9CE-10A-01D-A370-10 g.chr4:153245454C>T c.1737G>A c.(1735-1737)ggG>ggA p.G579G LIHC 4 153253841 153253841 + Missense_Mutation SNP G G T TCGA-FV-A4ZQ-01A-11D-A25V-10 TCGA-FV-A4ZQ-10A-01D-A25V-10 g.chr4:153253841G>T c.892C>A c.(892-894)Ccc>Acc p.P298T LIHC 4 153268212 153268212 + Missense_Mutation SNP A A G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr4:153268212A>G c.596T>C c.(595-597)cTt>cCt p.L199P LIHC 4 153273838 153273838 + Intron SNP A A T TCGA-CC-5259-01A-31D-A20W-10 TCGA-CC-5259-10A-01D-A20W-10 g.chr4:153273838A>T LUAD 4 153244298 153244298 + Missense_Mutation SNP G G C TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr4:153244298G>C c.1859C>G c.(1858-1860)cCc>cGc p.P620R LUAD 4 153245479 153245479 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr4:153245479C>A c.1712G>T c.(1711-1713)gGg>gTg p.G571V LUAD 4 153245480 153245480 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr4:153245480C>A c.1711G>T c.(1711-1713)Ggg>Tgg p.G571W LUAD 4 153247364 153247364 + Missense_Mutation SNP C C A TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chr4:153247364C>A c.1438G>T c.(1438-1440)Gat>Tat p.D480Y LUAD 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-17-Z037-01A-01W-0746-08 TCGA-17-Z037-11A-01W-0746-08 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H LUAD 4 153249457 153249457 + Missense_Mutation SNP G G A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr4:153249457G>A c.1321C>T c.(1321-1323)Cgg>Tgg p.R441W LUAD 4 153249469 153249469 + Nonsense_Mutation SNP C C A TCGA-38-7271-01A-11D-2036-08 TCGA-38-7271-11A-01D-2036-08 g.chr4:153249469C>A c.1309G>T c.(1309-1311)Gga>Tga p.G437* LUAD 4 153253847 153253847 + Silent SNP G G A TCGA-50-5933-01A-11D-1753-08 TCGA-50-5933-11A-01D-1753-08 g.chr4:153253847G>A c.886C>T c.(886-888)Ctg>Ttg p.L296L LUAD 4 153258956 153258956 + Missense_Mutation SNP C C T TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr4:153258956C>T c.859G>A c.(859-861)Gag>Aag p.E287K LUAD 4 153259062 153259062 + Frame_Shift_Del DEL A A - TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr4:153259062delA c.753delT c.(751-753)cttfs p.L251fs LUAD 4 153259073 153259073 + Nonsense_Mutation SNP C C A TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr4:153259073C>A c.742G>T c.(742-744)Gag>Tag p.E248* LUAD 4 153268138 153268138 + Nonsense_Mutation SNP G G A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr4:153268138G>A c.670C>T c.(670-672)Cga>Tga p.R224* LUAD 4 153273641 153273641 + Intron SNP A A G TCGA-55-7903-01A-11D-2167-08 TCGA-55-7903-10A-01D-2167-08 g.chr4:153273641A>G LUAD 4 153303398 153303398 + Intron SNP C C G TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr4:153303398C>G LUAD 4 153303400 153303400 + Intron SNP C C G TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr4:153303400C>G LUAD 4 153332524 153332524 + Silent SNP C C T TCGA-55-7284-01B-11D-2238-08 TCGA-55-7284-10A-01D-2238-08 g.chr4:153332524C>T c.432G>A c.(430-432)acG>acA p.T144T LUAD 4 153332619 153332619 + Nonsense_Mutation SNP C C A TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr4:153332619C>A c.337G>T c.(337-339)Gag>Tag p.E113* LUAD 4 153332652 153332652 + Missense_Mutation SNP C C T TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr4:153332652C>T c.304G>A c.(304-306)Gaa>Aaa p.E102K LUAD 4 153332826 153332826 + Nonsense_Mutation SNP G G A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr4:153332826G>A c.130C>T c.(130-132)Caa>Taa p.Q44* LUAD 4 153332934 153332934 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr4:153332934C>A c.22G>T c.(22-24)Gtg>Ttg p.V8L LUSC 4 153244124 153244124 + Nonsense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr4:153244124G>C c.2033C>G c.(2032-2034)tCa>tGa p.S678* LUSC 4 153244194 153244194 + Nonsense_Mutation SNP C C A TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr4:153244194C>A c.1963G>T c.(1963-1965)Gaa>Taa p.E655* LUSC 4 153244198 153244198 + Silent SNP C C G TCGA-33-4583-01A-01D-1441-08 TCGA-33-4583-11A-01D-1441-08 g.chr4:153244198C>G c.1959G>C c.(1957-1959)acG>acC p.T653T LUSC 4 153245437 153245437 + Missense_Mutation SNP C C G TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr4:153245437C>G c.1754G>C c.(1753-1755)aGt>aCt p.S585T LUSC 4 153247252 153247252 + Missense_Mutation SNP C C T TCGA-22-4604-01A-01D-1267-08 TCGA-22-4604-11A-01D-1267-08 g.chr4:153247252C>T c.1550G>A c.(1549-1551)gGa>gAa p.G517E LUSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G LUSC 4 153247289 153247289 + Missense_Mutation SNP G G C TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chr4:153247289G>C c.1513C>G c.(1513-1515)Cgc>Ggc p.R505G LUSC 4 153247289 153247289 + Missense_Mutation SNP G G T TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr4:153247289G>T c.1513C>A c.(1513-1515)Cgc>Agc p.R505S LUSC 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* LUSC 4 153247367 153247367 + Silent SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr4:153247367G>T c.1435C>A c.(1435-1437)Cga>Aga p.R479R LUSC 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H LUSC 4 153249410 153249410 + Silent SNP G G T TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr4:153249410G>T c.1368C>A c.(1366-1368)acC>acA p.T456T LUSC 4 153271243 153271243 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr4:153271243G>A c.535C>T c.(535-537)Cgc>Tgc p.R179C OV 4 153244205 153244205 + Nonsense_Mutation SNP A A T TCGA-24-1565-01A-01W-0551-08 TCGA-24-1565-10A-01W-0551-08 g.chr4:153244205A>T c.1952T>A c.(1951-1953)tTg>tAg p.L651* OV 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-25-1316-01A-01W-0494-09 TCGA-25-1316-10A-01W-0494-09 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C OV 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-04-1337-01A-01W-0484-10 TCGA-04-1337-11A-01W-0485-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H OV 4 153258956 153258956 + Missense_Mutation SNP C C G TCGA-36-2539-01A-01D-1526-09 TCGA-36-2539-10A-01D-1526-09 g.chr4:153258956C>G c.859G>C c.(859-861)Gag>Cag p.E287Q OV 4 153273826 153273826 + Intron SNP A A C TCGA-61-1903-01A-01W-0639-09 TCGA-61-1903-11A-01W-0640-09 g.chr4:153273826A>C OV 4 153273850 153273850 + Intron SNP G G T TCGA-29-1764-01A-01W-0633-09 TCGA-29-1764-10A-01W-0634-09 g.chr4:153273850G>T PAAD 4 153244139 153244139 + Nonsense_Mutation SNP C C T TCGA-2J-AABA-01A-21D-A40W-08 TCGA-2J-AABA-10A-01D-A40W-08 g.chr4:153244139C>T c.2018G>A c.(2017-2019)tGg>tAg p.W673* PAAD 4 153249472 153249473 + Frame_Shift_Ins INS - - AA TCGA-2J-AABT-01A-11D-A40W-08 TCGA-2J-AABT-10A-01D-A40W-08 g.chr4:153249472_153249473insAA c.1305_1306insTT c.(1303-1308)attagtfs p.S436fs PAAD 4 153250829 153250829 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:153250829C>T c.1231G>A c.(1231-1233)Ggc>Agc p.G411S PAAD 4 153253860 153253861 + Frame_Shift_Del DEL AT AT - TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr4:153253860_153253861delAT c.872_873delAT c.(871-873)tatfs p.Y291fs PAAD 4 153258977 153258977 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:153258977A>G c.838T>C c.(838-840)Ttc>Ctc p.F280L PAAD 4 153332931 153332931 + Missense_Mutation SNP C C T TCGA-HZ-7918-01A-11D-2154-08 TCGA-HZ-7918-10A-01D-2154-08 g.chr4:153332931C>T c.25G>A c.(25-27)Ggc>Agc p.G9S READ 4 153244078 153244078 + Silent SNP T T C TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr4:153244078T>C c.2079A>G c.(2077-2079)gaA>gaG p.E693E READ 4 153244079 153244079 + Missense_Mutation SNP T T C TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153244079T>C c.2078A>G c.(2077-2079)gAa>gGa p.E693G READ 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* READ 4 153244185 153244185 + Nonsense_Mutation SNP G G A TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr4:153244185G>A c.1972C>T c.(1972-1974)Cga>Tga p.R658* READ 4 153245393 153245393 + Missense_Mutation SNP C C A TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr4:153245393C>A c.1798G>T c.(1798-1800)Gat>Tat p.D600Y READ 4 153245398 153245398 + Missense_Mutation SNP T T C TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr4:153245398T>C c.1793A>G c.(1792-1794)aAt>aGt p.N598S READ 4 153245445 153245445 + Silent SNP C C T TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr4:153245445C>T c.1746G>A c.(1744-1746)tcG>tcA p.S582S READ 4 153245445 153245445 + Silent SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153245445C>T c.1746G>A c.(1744-1746)tcG>tcA p.S582S READ 4 153245446 153245446 + Missense_Mutation SNP G G A TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr4:153245446G>A c.1745C>T c.(1744-1746)tCg>tTg p.S582L READ 4 153245453 153245453 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153245453G>A c.1738C>T c.(1738-1740)Cac>Tac p.H580Y READ 4 153247169 153247169 + Missense_Mutation SNP A A G TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr4:153247169A>G c.1633T>C c.(1633-1635)Tat>Cat p.Y545H READ 4 153247183 153247183 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153247183T>C c.1619A>G c.(1618-1620)cAt>cGt p.H540R READ 4 153247208 153247208 + Missense_Mutation SNP T T C TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:153247208T>C c.1594A>G c.(1594-1596)Acc>Gcc p.T532A READ 4 153247289 153247289 + Missense_Mutation SNP G G A TCGA-AG-3885-01A-01W-0899-10 TCGA-AG-3885-10A-01W-0901-10 g.chr4:153247289G>A c.1513C>T c.(1513-1515)Cgc>Tgc p.R505C READ 4 153247318 153247318 + Missense_Mutation SNP T T G TCGA-AG-3600-01A-01W-0833-10 TCGA-AG-3600-10A-01W-0833-10 g.chr4:153247318T>G c.1484A>C c.(1483-1485)cAt>cCt p.H495P READ 4 153247327 153247327 + Frame_Shift_Del DEL T T - TCGA-CI-6620-01A-11D-1826-10 TCGA-CI-6620-10A-01D-1826-10 g.chr4:153247327delT c.1475delA c.(1474-1476)cagfs p.Q492fs READ 4 153247363 153247363 + Missense_Mutation SNP T T C TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr4:153247363T>C c.1439A>G c.(1438-1440)gAt>gGt p.D480G READ 4 153247367 153247367 + Nonsense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr4:153247367G>A c.1435C>T c.(1435-1437)Cga>Tga p.R479* READ 4 153249360 153249361 + Splice_Site INS - - T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153249360_153249361insT c.1417_1418insA c.(1417-1419)aga>aAga p.R473fs READ 4 153249369 153249369 + Missense_Mutation SNP T T C TCGA-DC-6158-01A-11D-1657-10 TCGA-DC-6158-10A-01D-1657-10 g.chr4:153249369T>C c.1409A>G c.(1408-1410)cAt>cGt p.H470R READ 4 153249383 153249383 + Silent SNP A A G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R READ 4 153249383 153249383 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr4:153249383A>G c.1395T>C c.(1393-1395)cgT>cgC p.R465R READ 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AG-3608-01A-01W-0833-10 TCGA-AG-3608-10A-01W-0833-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H READ 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-AG-3881-01A-01W-0899-10 TCGA-AG-3881-10A-01W-0901-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H READ 4 153249384 153249384 + Missense_Mutation SNP C C T TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr4:153249384C>T c.1394G>A c.(1393-1395)cGt>cAt p.R465H READ 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AG-3898-01A-01W-1073-09 TCGA-AG-3898-10A-01W-1073-09 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C READ 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C READ 4 153249385 153249385 + Missense_Mutation SNP G G A TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr4:153249385G>A c.1393C>T c.(1393-1395)Cgt>Tgt p.R465C READ 4 153249451 153249451 + Missense_Mutation SNP G G A TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153249451G>A c.1327C>T c.(1327-1329)Ctc>Ttc p.L443F READ 4 153249456 153249456 + Missense_Mutation SNP C C A TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr4:153249456C>A c.1322G>T c.(1321-1323)cGg>cTg p.R441L READ 4 153249460 153249460 + Missense_Mutation SNP C C A TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr4:153249460C>A c.1318G>T c.(1318-1320)Gat>Tat p.D440Y READ 4 153249466 153249466 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr4:153249466A>G c.1312T>C c.(1312-1314)Tct>Cct p.S438P READ 4 153249469 153249469 + Missense_Mutation SNP C C T TCGA-AG-A011-01A-01W-A00K-09 TCGA-AG-A011-10A-01W-A00K-09 g.chr4:153249469C>T c.1309G>A c.(1309-1311)Gga>Aga p.G437R READ 4 153250856 153250858 + In_Frame_Del DEL TGT TGT - TCGA-AG-3594-01A-02W-0831-10 TCGA-AG-3594-10A-01W-0831-10 g.chr4:153250856_153250858delTGT c.1202_1204delACA c.(1201-1206)aacact>act p.N401del READ 4 153251901 153251901 + Nonsense_Mutation SNP C C A TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr4:153251901C>A c.1105G>T c.(1105-1107)Gaa>Taa p.E369* READ 4 153251905 153251905 + Silent SNP T T C TCGA-AH-6547-01A-11D-1826-10 TCGA-AH-6547-11A-02D-1826-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R READ 4 153251905 153251905 + Silent SNP T T C TCGA-EI-6508-01A-11D-1733-10 TCGA-EI-6508-10A-01D-1733-10 g.chr4:153251905T>C c.1101A>G c.(1099-1101)cgA>cgG p.R367R READ 4 153253790 153253790 + Missense_Mutation SNP C C T TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr4:153253790C>T c.943G>A c.(943-945)Gct>Act p.A315T READ 4 153253824 153253824 + Silent SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153253824T>C c.909A>G c.(907-909)caA>caG p.Q303Q READ 4 153258969 153258969 + Silent SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr4:153258969T>C c.846A>G c.(844-846)tcA>tcG p.S282S READ 4 153258971 153258971 + Missense_Mutation SNP A A T TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr4:153258971A>T c.844T>A c.(844-846)Tca>Aca p.S282T READ 4 153258991 153258995 + Frame_Shift_Del DEL TGGGG TGGGG - TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr4:153258991_153258995delTGGGG c.820_824delCCCCA c.(820-825)ccccagfs p.PQ274fs READ 4 153268093 153268093 + Missense_Mutation SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153268093T>G c.715A>C c.(715-717)Aaa>Caa p.K239Q READ 4 153271206 153271206 + Nonsense_Mutation SNP G G C TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr4:153271206G>C c.572C>G c.(571-573)tCa>tGa p.S191* READ 4 153271242 153271242 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153271242C>T c.536G>A c.(535-537)cGc>cAc p.R179H READ 4 153273871 153273871 + Intron SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:153273871C>T READ 4 153332662 153332662 + Silent SNP T T C TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr4:153332662T>C c.294A>G c.(292-294)caA>caG p.Q98Q READ 4 153332915 153332915 + Missense_Mutation SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr4:153332915C>T c.41G>A c.(40-42)cGa>cAa p.R14Q READ 4 153332917 153332917 + Silent SNP T T C TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr4:153332917T>C c.39A>G c.(37-39)cgA>cgG p.R13R READ 4 153332919 153332919 + Nonsense_Mutation SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:153332919G>A c.37C>T c.(37-39)Cga>Tga p.R13* SARC 4 153271229 153271229 + Silent SNP C C T TCGA-DX-A8BS-01A-11D-A37C-09 TCGA-DX-A8BS-11A-13D-A37F-09 g.chr4:153271229C>T c.549G>A c.(547-549)ttG>ttA p.L183L SKCM 4 153245389 153245389 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr4:153245389G>A c.1802C>T c.(1801-1803)tCt>tTt p.S601F SKCM 4 153247170 153247170 + Silent SNP G G C TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr4:153247170G>C c.1632C>G c.(1630-1632)gtC>gtG p.V544V SKCM 4 153247254 153247254 + Missense_Mutation SNP A A C TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr4:153247254A>C c.1548T>G c.(1546-1548)agT>agG p.S516R SKCM 4 153247304 153247304 + Missense_Mutation SNP G G A TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr4:153247304G>A c.1498C>T c.(1498-1500)Cat>Tat p.H500Y SKCM 4 153247366 153247366 + Missense_Mutation SNP C C T TCGA-FS-A1YY-06A-11D-A197-08 TCGA-FS-A1YY-10A-01D-A199-08 g.chr4:153247366C>T c.1436G>A c.(1435-1437)cGa>cAa p.R479Q SKCM 4 153251903 153251903 + Missense_Mutation SNP C C T TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr4:153251903C>T c.1103G>A c.(1102-1104)gGa>gAa p.G368E SKCM 4 153253809 153253809 + Nonsense_Mutation SNP A A T TCGA-GN-A4U9-06A-11D-A32N-08 TCGA-GN-A4U9-10B-01D-A32N-08 g.chr4:153253809A>T c.924T>A c.(922-924)tgT>tgA p.C308* SKCM 4 153253840 153253840 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr4:153253840G>A c.893C>T c.(892-894)cCc>cTc p.P298L SKCM 4 153268087 153268087 + Missense_Mutation SNP A A G TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr4:153268087A>G c.721T>C c.(721-723)Ttt>Ctt p.F241L SKCM 4 153271233 153271233 + Missense_Mutation SNP G G A TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr4:153271233G>A c.545C>T c.(544-546)tCt>tTt p.S182F SKCM 4 153332598 153332598 + Nonsense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr4:153332598G>A c.358C>T c.(358-360)Cag>Tag p.Q120* SKCM 4 153332598 153332598 + Nonsense_Mutation SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr4:153332598G>A c.358C>T c.(358-360)Cag>Tag p.Q120*

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 4 153247212 153247212 single base substitution A C downstream_gene_variant BLCA-CN 4 153247212 153247212 single base substitution A C exon_variant BLCA-CN 4 153247212 153247212 single base substitution A C synonymous_variant T354T 1062T>G BLCA-CN 4 153247212 153247212 single base substitution A C synonymous_variant T412T 1236T>G BLCA-CN 4 153247212 153247212 single base substitution A C synonymous_variant T450T 1350T>G BLCA-CN 4 153247212 153247212 single base substitution A C synonymous_variant T530T 1590T>G BLCA-CN 4 153247212 153247212 single base substitution A C upstream_gene_variant BLCA-CN 4 153247244 153247244 single base substitution C T downstream_gene_variant BLCA-CN 4 153247244 153247244 single base substitution C T exon_variant BLCA-CN 4 153247244 153247244 single base substitution C T missense_variant D344N 1030G>A BLCA-CN 4 153247244 153247244 single base substitution C T missense_variant D402N 1204G>A BLCA-CN 4 153247244 153247244 single base substitution C T missense_variant D440N 1318G>A BLCA-CN 4 153247244 153247244 single base substitution C T missense_variant D520N 1558G>A BLCA-CN 4 153247244 153247244 single base substitution C T upstream_gene_variant BLCA-CN 4 153249467 153249467 single base substitution T A exon_variant BLCA-CN 4 153249467 153249467 single base substitution T A synonymous_variant G261G 783A>T BLCA-CN 4 153249467 153249467 single base substitution T A synonymous_variant G319G 957A>T BLCA-CN 4 153249467 153249467 single base substitution T A synonymous_variant G357G 1071A>T BLCA-CN 4 153249467 153249467 single base substitution T A synonymous_variant G437G 1311A>T BLCA-CN 4 153249467 153249467 single base substitution T A upstream_gene_variant BLCA-CN 4 153253860 153253860 single base substitution A T exon_variant BLCA-CN 4 153253860 153253860 single base substitution A T stop_gained Y115* 345T>A BLCA-CN 4 153253860 153253860 single base substitution A T stop_gained Y173* 519T>A BLCA-CN 4 153253860 153253860 single base substitution A T stop_gained Y211* 633T>A BLCA-CN 4 153253860 153253860 single base substitution A T stop_gained Y291* 873T>A BLCA-CN 4 153253860 153253860 single base substitution A T upstream_gene_variant BLCA-CN 4 153273761 153273761 single base substitution G A exon_variant BLCA-CN 4 153273761 153273761 single base substitution G A intron_variant BLCA-CN 4 153273761 153273761 single base substitution G A missense_variant S41F 122C>T BLCA-CN 4 153273761 153273761 single base substitution G A upstream_gene_variant BOCA-FR 4 153345430 153345430 single base substitution G C intron_variant BRCA-EU 4 153239072 153239072 single base substitution C G downstream_gene_variant BRCA-EU 4 153240567 153240567 deletion of <=200bp G - downstream_gene_variant BRCA-EU 4 153242413 153242413 single base substitution C A 3_prime_UTR_variant BRCA-EU 4 153242413 153242413 single base substitution C A downstream_gene_variant BRCA-EU 4 153243896 153243896 single base substitution C G 3_prime_UTR_variant BRCA-EU 4 153243896 153243896 single base substitution C G downstream_gene_variant BRCA-EU 4 153243928 153243928 single base substitution A T 3_prime_UTR_variant BRCA-EU 4 153243928 153243928 single base substitution A T downstream_gene_variant BRCA-EU 4 153244505 153244505 single base substitution A G downstream_gene_variant BRCA-EU 4 153244505 153244505 single base substitution A G exon_variant BRCA-EU 4 153244505 153244505 single base substitution A G intron_variant BRCA-EU 4 153246463 153246463 single base substitution A G downstream_gene_variant BRCA-EU 4 153246463 153246463 single base substitution A G exon_variant BRCA-EU 4 153246463 153246463 single base substitution A G intron_variant BRCA-EU 4 153246463 153246463 single base substitution A G upstream_gene_variant BRCA-EU 4 153247289 153247289 single base substitution G A downstream_gene_variant BRCA-EU 4 153247289 153247289 single base substitution G A exon_variant BRCA-EU 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T BRCA-EU 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T BRCA-EU 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T BRCA-EU 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T BRCA-EU 4 153247289 153247289 single base substitution G A upstream_gene_variant BRCA-EU 4 153247831 153247831 single base substitution C T intron_variant BRCA-EU 4 153247831 153247831 single base substitution C T upstream_gene_variant BRCA-EU 4 153248307 153248307 single base substitution G A intron_variant BRCA-EU 4 153248307 153248307 single base substitution G A upstream_gene_variant BRCA-EU 4 153249780 153249780 single base substitution G C exon_variant BRCA-EU 4 153249780 153249780 single base substitution G C intron_variant BRCA-EU 4 153249780 153249780 single base substitution G C upstream_gene_variant BRCA-EU 4 153251336 153251336 deletion of <=200bp A - intron_variant BRCA-EU 4 153251336 153251336 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 153252684 153252684 single base substitution G A intron_variant BRCA-EU 4 153252684 153252684 single base substitution G A upstream_gene_variant BRCA-EU 4 153254633 153254633 deletion of <=200bp A - intron_variant BRCA-EU 4 153254633 153254633 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 153254826 153254826 single base substitution A C intron_variant BRCA-EU 4 153254826 153254826 single base substitution A C upstream_gene_variant BRCA-EU 4 153255400 153255400 single base substitution T C intron_variant BRCA-EU 4 153255400 153255400 single base substitution T C upstream_gene_variant BRCA-EU 4 153256493 153256493 single base substitution G A intron_variant BRCA-EU 4 153256493 153256493 single base substitution G A upstream_gene_variant BRCA-EU 4 153258985 153258985 single base substitution T G missense_variant Q101P 302A>C BRCA-EU 4 153258985 153258985 single base substitution T G missense_variant Q159P 476A>C BRCA-EU 4 153258985 153258985 single base substitution T G missense_variant Q197P 590A>C BRCA-EU 4 153258985 153258985 single base substitution T G missense_variant Q277P 830A>C BRCA-EU 4 153259008 153259010 deletion of <=200bp CAT - inframe_deletion M151 BRCA-EU 4 153259008 153259010 deletion of <=200bp CAT - inframe_deletion M189 BRCA-EU 4 153259008 153259010 deletion of <=200bp CAT - inframe_deletion M269 BRCA-EU 4 153259008 153259010 deletion of <=200bp CAT - inframe_deletion M93 BRCA-EU 4 153259118 153259118 deletion of <=200bp T - intron_variant BRCA-EU 4 153261214 153261214 single base substitution G T intron_variant BRCA-EU 4 153263785 153263785 single base substitution C G downstream_gene_variant BRCA-EU 4 153263785 153263785 single base substitution C G intron_variant BRCA-EU 4 153264614 153264614 single base substitution T A downstream_gene_variant BRCA-EU 4 153264614 153264614 single base substitution T A intron_variant BRCA-EU 4 153264871 153264871 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 153264871 153264871 deletion of <=200bp A - intron_variant BRCA-EU 4 153264923 153264923 single base substitution C A downstream_gene_variant BRCA-EU 4 153264923 153264923 single base substitution C A intron_variant BRCA-EU 4 153265545 153265545 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 153265545 153265545 deletion of <=200bp A - intron_variant BRCA-EU 4 153266142 153266142 single base substitution G C downstream_gene_variant BRCA-EU 4 153266142 153266142 single base substitution G C intron_variant BRCA-EU 4 153266214 153266214 single base substitution G T downstream_gene_variant BRCA-EU 4 153266214 153266214 single base substitution G T intron_variant BRCA-EU 4 153267876 153267876 single base substitution A G downstream_gene_variant BRCA-EU 4 153267876 153267876 single base substitution A G intron_variant BRCA-EU 4 153268084 153268084 single base substitution G A exon_variant BRCA-EU 4 153268084 153268084 single base substitution G A stop_gained Q124* 370C>T BRCA-EU 4 153268084 153268084 single base substitution G A stop_gained Q162* 484C>T BRCA-EU 4 153268084 153268084 single base substitution G A stop_gained Q242* 724C>T BRCA-EU 4 153268084 153268084 single base substitution G A stop_gained Q66* 196C>T BRCA-EU 4 153271497 153271497 single base substitution G A intron_variant BRCA-EU 4 153271497 153271497 single base substitution G A upstream_gene_variant BRCA-EU 4 153272755 153272755 single base substitution T C intron_variant BRCA-EU 4 153272755 153272755 single base substitution T C upstream_gene_variant BRCA-EU 4 153273572 153273572 single base substitution C A intron_variant BRCA-EU 4 153273572 153273572 single base substitution C A upstream_gene_variant BRCA-EU 4 153274430 153274430 single base substitution G C intron_variant BRCA-EU 4 153274430 153274430 single base substitution G C upstream_gene_variant BRCA-EU 4 153274909 153274909 single base substitution G A intron_variant BRCA-EU 4 153274909 153274909 single base substitution G A upstream_gene_variant BRCA-EU 4 153275489 153275489 deletion of <=200bp A - intron_variant BRCA-EU 4 153275489 153275489 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 153275576 153275576 insertion of <=200bp - A intron_variant BRCA-EU 4 153275576 153275576 insertion of <=200bp - A upstream_gene_variant BRCA-EU 4 153276532 153276532 deletion of <=200bp T - intron_variant BRCA-EU 4 153276532 153276532 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 153280365 153280365 single base substitution T C intron_variant BRCA-EU 4 153281585 153281585 single base substitution G A intron_variant BRCA-EU 4 153284750 153284750 single base substitution T C intron_variant BRCA-EU 4 153286268 153286268 single base substitution G C intron_variant BRCA-EU 4 153288425 153288425 deletion of <=200bp A - intron_variant BRCA-EU 4 153289717 153289717 single base substitution A G intron_variant BRCA-EU 4 153293721 153293721 single base substitution C A intron_variant BRCA-EU 4 153297847 153297847 deletion of <=200bp T - intron_variant BRCA-EU 4 153299481 153299481 single base substitution G A intron_variant BRCA-EU 4 153300669 153300669 single base substitution C T intron_variant BRCA-EU 4 153303266 153303266 single base substitution G T intron_variant BRCA-EU 4 153304139 153304139 single base substitution C G intron_variant BRCA-EU 4 153304139 153304139 single base substitution C G upstream_gene_variant BRCA-EU 4 153305544 153305544 single base substitution T C intron_variant BRCA-EU 4 153305544 153305544 single base substitution T C upstream_gene_variant BRCA-EU 4 153306492 153306492 single base substitution C T intron_variant BRCA-EU 4 153306492 153306492 single base substitution C T upstream_gene_variant BRCA-EU 4 153307659 153307659 single base substitution T A intron_variant BRCA-EU 4 153307659 153307659 single base substitution T A upstream_gene_variant BRCA-EU 4 153309930 153309930 single base substitution C G intron_variant BRCA-EU 4 153312590 153312590 single base substitution C G intron_variant BRCA-EU 4 153312748 153312748 single base substitution A T intron_variant BRCA-EU 4 153313046 153313046 single base substitution C A intron_variant BRCA-EU 4 153316216 153316216 single base substitution G A intron_variant BRCA-EU 4 153318134 153318134 single base substitution G A intron_variant BRCA-EU 4 153319494 153319494 single base substitution A T intron_variant BRCA-EU 4 153319692 153319692 deletion of <=200bp A - intron_variant BRCA-EU 4 153321036 153321036 single base substitution A G intron_variant BRCA-EU 4 153324428 153324428 single base substitution G A intron_variant BRCA-EU 4 153325760 153325760 single base substitution A G intron_variant BRCA-EU 4 153326197 153326197 single base substitution T C intron_variant BRCA-EU 4 153326677 153326677 single base substitution G A intron_variant BRCA-EU 4 153329502 153329502 single base substitution A T downstream_gene_variant BRCA-EU 4 153329502 153329502 single base substitution A T intron_variant BRCA-EU 4 153329834 153329837 deletion of <=200bp CTGA - downstream_gene_variant BRCA-EU 4 153329834 153329837 deletion of <=200bp CTGA - intron_variant BRCA-EU 4 153331387 153331387 single base substitution G A downstream_gene_variant BRCA-EU 4 153331387 153331387 single base substitution G A intron_variant BRCA-EU 4 153331540 153331540 single base substitution C T downstream_gene_variant BRCA-EU 4 153331540 153331540 single base substitution C T intron_variant BRCA-EU 4 153331576 153331576 single base substitution T C downstream_gene_variant BRCA-EU 4 153331576 153331576 single base substitution T C intron_variant BRCA-EU 4 153331592 153331592 single base substitution A G downstream_gene_variant BRCA-EU 4 153331592 153331592 single base substitution A G intron_variant BRCA-EU 4 153332198 153332198 single base substitution G A downstream_gene_variant BRCA-EU 4 153332198 153332198 single base substitution G A intron_variant BRCA-EU 4 153332652 153332652 single base substitution C T missense_variant E102K 304G>A BRCA-EU 4 153332811 153332811 single base substitution C A stop_gained E49* 145G>T BRCA-EU 4 153334353 153334353 single base substitution C A intron_variant BRCA-EU 4 153334353 153334353 single base substitution C A upstream_gene_variant BRCA-EU 4 153334355 153334355 deletion of <=200bp A - intron_variant BRCA-EU 4 153334355 153334355 deletion of <=200bp A - upstream_gene_variant BRCA-EU 4 153336082 153336082 single base substitution G C intron_variant BRCA-EU 4 153336082 153336082 single base substitution G C upstream_gene_variant BRCA-EU 4 153336343 153336343 single base substitution A G intron_variant BRCA-EU 4 153336343 153336343 single base substitution A G upstream_gene_variant BRCA-EU 4 153338076 153338076 single base substitution G A intron_variant BRCA-EU 4 153338076 153338076 single base substitution G A upstream_gene_variant BRCA-EU 4 153341185 153341185 single base substitution G A intron_variant BRCA-EU 4 153342082 153342082 single base substitution G C intron_variant BRCA-EU 4 153345928 153345928 single base substitution G A intron_variant BRCA-EU 4 153347575 153347595 deletion of <=200bp CACTGTAGCCTCCGCCTCCCG - intron_variant BRCA-EU 4 153353167 153353167 single base substitution T C intron_variant BRCA-EU 4 153354101 153354101 single base substitution G A intron_variant BRCA-EU 4 153354388 153354388 single base substitution T G intron_variant BRCA-EU 4 153355250 153355250 single base substitution T C intron_variant BRCA-EU 4 153355359 153355359 single base substitution C A intron_variant BRCA-EU 4 153358710 153358711 deletion of <=200bp TT - intron_variant BRCA-EU 4 153361930 153361930 single base substitution C T intron_variant BRCA-EU 4 153363507 153363507 single base substitution C A intron_variant BRCA-EU 4 153366331 153366331 single base substitution G C intron_variant BRCA-EU 4 153366577 153366577 single base substitution C G intron_variant BRCA-EU 4 153366807 153366807 single base substitution C G intron_variant BRCA-EU 4 153367465 153367465 insertion of <=200bp - C intron_variant BRCA-EU 4 153369464 153369464 single base substitution G C intron_variant BRCA-EU 4 153373182 153373182 single base substitution A C intron_variant BRCA-EU 4 153374336 153374336 insertion of <=200bp - A intron_variant BRCA-EU 4 153374371 153374371 single base substitution G C intron_variant BRCA-EU 4 153377555 153377555 single base substitution G C intron_variant BRCA-EU 4 153381091 153381099 deletion of <=200bp AAATTCATA - intron_variant BRCA-EU 4 153381614 153381614 single base substitution T A intron_variant BRCA-EU 4 153381658 153381658 single base substitution G A intron_variant BRCA-EU 4 153381942 153381942 single base substitution T A intron_variant BRCA-EU 4 153382905 153382905 single base substitution C T intron_variant BRCA-EU 4 153383173 153383173 single base substitution G C intron_variant BRCA-EU 4 153385229 153385229 single base substitution G A intron_variant BRCA-EU 4 153386471 153386471 single base substitution G A intron_variant BRCA-EU 4 153386757 153386757 single base substitution G T intron_variant BRCA-EU 4 153387869 153387869 single base substitution C T intron_variant BRCA-EU 4 153388458 153388460 deletion of <=200bp CTC - intron_variant BRCA-EU 4 153389509 153389509 single base substitution G C intron_variant BRCA-EU 4 153390229 153390229 single base substitution T A intron_variant BRCA-EU 4 153391668 153391668 single base substitution G A intron_variant BRCA-EU 4 153393033 153393033 single base substitution C G intron_variant BRCA-EU 4 153393186 153393186 single base substitution A G intron_variant BRCA-EU 4 153393823 153393823 single base substitution G C intron_variant BRCA-EU 4 153397096 153397096 single base substitution A G intron_variant BRCA-EU 4 153398497 153398497 single base substitution T C intron_variant BRCA-EU 4 153403059 153403059 single base substitution T C intron_variant BRCA-EU 4 153404837 153404837 single base substitution G T intron_variant BRCA-EU 4 153412182 153412182 single base substitution G A intron_variant BRCA-EU 4 153415243 153415243 single base substitution G A intron_variant BRCA-EU 4 153415294 153415294 deletion of <=200bp A - intron_variant BRCA-EU 4 153415361 153415361 single base substitution C T intron_variant BRCA-EU 4 153416148 153416148 single base substitution G A intron_variant BRCA-EU 4 153416410 153416410 single base substitution C A intron_variant BRCA-EU 4 153416430 153416430 single base substitution T A intron_variant BRCA-EU 4 153416874 153416874 single base substitution C T intron_variant BRCA-EU 4 153417230 153417230 single base substitution G C intron_variant BRCA-EU 4 153417310 153417310 single base substitution C G intron_variant BRCA-EU 4 153418370 153418370 single base substitution G C intron_variant BRCA-EU 4 153419658 153419658 single base substitution G T intron_variant BRCA-EU 4 153422039 153422039 single base substitution A T intron_variant BRCA-EU 4 153422518 153422518 single base substitution A G intron_variant BRCA-EU 4 153422555 153422555 single base substitution C T intron_variant BRCA-EU 4 153425580 153425580 single base substitution G C intron_variant BRCA-EU 4 153425760 153425760 deletion of <=200bp A - intron_variant BRCA-EU 4 153425930 153425930 single base substitution G T intron_variant BRCA-EU 4 153425970 153425970 deletion of <=200bp T - intron_variant BRCA-EU 4 153426076 153426076 single base substitution T A intron_variant BRCA-EU 4 153426622 153426622 single base substitution A G intron_variant BRCA-EU 4 153426785 153426785 single base substitution C A intron_variant BRCA-EU 4 153426878 153426878 single base substitution C A intron_variant BRCA-EU 4 153428071 153428071 single base substitution T C intron_variant BRCA-EU 4 153428157 153428157 single base substitution C G intron_variant BRCA-EU 4 153428748 153428748 single base substitution A T intron_variant BRCA-EU 4 153428805 153428805 single base substitution G A intron_variant BRCA-EU 4 153429012 153429012 single base substitution T C intron_variant BRCA-EU 4 153429742 153429742 single base substitution G A intron_variant BRCA-EU 4 153430010 153430010 single base substitution T A intron_variant BRCA-EU 4 153430894 153430894 single base substitution G A intron_variant BRCA-EU 4 153431506 153431506 single base substitution A G intron_variant BRCA-EU 4 153431930 153431930 single base substitution G A intron_variant BRCA-EU 4 153435128 153435128 single base substitution C T intron_variant BRCA-EU 4 153436593 153436593 deletion of <=200bp G - intron_variant BRCA-EU 4 153440232 153440232 single base substitution C A intron_variant BRCA-EU 4 153440233 153440233 single base substitution G C intron_variant BRCA-EU 4 153441713 153441713 single base substitution C T intron_variant BRCA-EU 4 153443634 153443634 single base substitution T C intron_variant BRCA-EU 4 153445096 153445096 single base substitution G A intron_variant BRCA-EU 4 153445742 153445742 single base substitution C T intron_variant BRCA-EU 4 153445994 153445994 single base substitution C T intron_variant BRCA-EU 4 153448658 153448658 single base substitution G A downstream_gene_variant BRCA-EU 4 153448658 153448658 single base substitution G A intron_variant BRCA-EU 4 153448772 153448772 single base substitution A T downstream_gene_variant BRCA-EU 4 153448772 153448772 single base substitution A T intron_variant BRCA-EU 4 153450136 153450136 single base substitution G A downstream_gene_variant BRCA-EU 4 153450136 153450136 single base substitution G A intron_variant BRCA-EU 4 153450203 153450203 single base substitution C G downstream_gene_variant BRCA-EU 4 153450203 153450203 single base substitution C G intron_variant BRCA-EU 4 153450474 153450474 single base substitution T G downstream_gene_variant BRCA-EU 4 153450474 153450474 single base substitution T G intron_variant BRCA-EU 4 153451701 153451701 single base substitution G T exon_variant BRCA-EU 4 153451701 153451701 single base substitution G T intron_variant BRCA-EU 4 153453254 153453254 single base substitution T C intron_variant BRCA-EU 4 153453917 153453917 insertion of <=200bp - T intron_variant BRCA-EU 4 153454940 153454940 deletion of <=200bp A - intron_variant BRCA-EU 4 153456686 153456686 single base substitution C G 5_prime_UTR_variant BRCA-EU 4 153456686 153456686 single base substitution C G upstream_gene_variant BRCA-EU 4 153461310 153461310 single base substitution A G upstream_gene_variant BRCA-EU 4 153461407 153461408 deletion of <=200bp TC - upstream_gene_variant BRCA-FR 4 153239072 153239072 single base substitution C G downstream_gene_variant BRCA-FR 4 153239280 153239280 single base substitution G A downstream_gene_variant BRCA-FR 4 153243928 153243928 single base substitution A T 3_prime_UTR_variant BRCA-FR 4 153243928 153243928 single base substitution A T downstream_gene_variant BRCA-FR 4 153249780 153249780 single base substitution G C exon_variant BRCA-FR 4 153249780 153249780 single base substitution G C intron_variant BRCA-FR 4 153249780 153249780 single base substitution G C upstream_gene_variant BRCA-FR 4 153256028 153256028 single base substitution C G intron_variant BRCA-FR 4 153256028 153256028 single base substitution C G upstream_gene_variant BRCA-FR 4 153262195 153262195 single base substitution G A intron_variant BRCA-FR 4 153264923 153264923 single base substitution C A downstream_gene_variant BRCA-FR 4 153264923 153264923 single base substitution C A intron_variant BRCA-FR 4 153270107 153270107 single base substitution G C intron_variant BRCA-FR 4 153270107 153270107 single base substitution G C upstream_gene_variant BRCA-FR 4 153305544 153305544 single base substitution T C intron_variant BRCA-FR 4 153305544 153305544 single base substitution T C upstream_gene_variant BRCA-FR 4 153307659 153307659 single base substitution T A intron_variant BRCA-FR 4 153307659 153307659 single base substitution T A upstream_gene_variant BRCA-FR 4 153309930 153309930 single base substitution C G intron_variant BRCA-FR 4 153312748 153312748 single base substitution A T intron_variant BRCA-FR 4 153322789 153322789 single base substitution C A intron_variant BRCA-FR 4 153326197 153326197 single base substitution T C intron_variant BRCA-FR 4 153332198 153332198 single base substitution G A downstream_gene_variant BRCA-FR 4 153332198 153332198 single base substitution G A intron_variant BRCA-FR 4 153366331 153366331 single base substitution G C intron_variant BRCA-FR 4 153368624 153368624 single base substitution T C intron_variant BRCA-FR 4 153372072 153372072 single base substitution G A intron_variant BRCA-FR 4 153417230 153417230 single base substitution G C intron_variant BRCA-FR 4 153418370 153418370 single base substitution G C intron_variant BRCA-FR 4 153426878 153426878 single base substitution C A intron_variant BRCA-FR 4 153428157 153428157 single base substitution C G intron_variant BRCA-FR 4 153428589 153428589 single base substitution C G intron_variant BRCA-FR 4 153428805 153428805 single base substitution G A intron_variant BRCA-FR 4 153429012 153429012 single base substitution T C intron_variant BRCA-FR 4 153430536 153430536 single base substitution G A intron_variant BRCA-FR 4 153454105 153454105 single base substitution G A intron_variant BRCA-FR 4 153461118 153461118 single base substitution C T upstream_gene_variant BRCA-FR 4 153461208 153461208 single base substitution C G upstream_gene_variant BRCA-KR 4 153269959 153269959 single base substitution G C intron_variant BRCA-KR 4 153269959 153269959 single base substitution G C upstream_gene_variant BRCA-UK 4 153242413 153242413 single base substitution C A 3_prime_UTR_variant BRCA-UK 4 153242413 153242413 single base substitution C A downstream_gene_variant BRCA-UK 4 153244505 153244505 single base substitution A G downstream_gene_variant BRCA-UK 4 153244505 153244505 single base substitution A G exon_variant BRCA-UK 4 153244505 153244505 single base substitution A G intron_variant BRCA-UK 4 153249456 153249456 single base substitution C A exon_variant BRCA-UK 4 153249456 153249456 single base substitution C A missense_variant R265L 794G>T BRCA-UK 4 153249456 153249456 single base substitution C A missense_variant R323L 968G>T BRCA-UK 4 153249456 153249456 single base substitution C A missense_variant R361L 1082G>T BRCA-UK 4 153249456 153249456 single base substitution C A missense_variant R441L 1322G>T BRCA-UK 4 153249456 153249456 single base substitution C A upstream_gene_variant BRCA-UK 4 153332702 153332702 single base substitution A C missense_variant I85S 254T>G BRCA-UK 4 153332712 153332712 single base substitution T A missense_variant N82Y 244A>T BRCA-UK 4 153336082 153336082 single base substitution G C intron_variant BRCA-UK 4 153336082 153336082 single base substitution G C upstream_gene_variant BRCA-UK 4 153381942 153381942 single base substitution T A intron_variant BRCA-UK 4 153422555 153422555 single base substitution C T intron_variant BRCA-UK 4 153453254 153453254 single base substitution T C intron_variant BRCA-US 4 153244156 153244156 deletion of <=200bp C - downstream_gene_variant BRCA-US 4 153244156 153244156 deletion of <=200bp C - exon_variant BRCA-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G491 BRCA-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G549 BRCA-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G587 BRCA-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G667 BRCA-US 4 153247168 153247168 single base substitution T C downstream_gene_variant BRCA-US 4 153247168 153247168 single base substitution T C exon_variant BRCA-US 4 153247168 153247168 single base substitution T C missense_variant Y369C 1106A>G BRCA-US 4 153247168 153247168 single base substitution T C missense_variant Y427C 1280A>G BRCA-US 4 153247168 153247168 single base substitution T C missense_variant Y465C 1394A>G BRCA-US 4 153247168 153247168 single base substitution T C missense_variant Y545C 1634A>G BRCA-US 4 153247168 153247168 single base substitution T C upstream_gene_variant BRCA-US 4 153247265 153247265 single base substitution T C downstream_gene_variant BRCA-US 4 153247265 153247265 single base substitution T C exon_variant BRCA-US 4 153247265 153247265 single base substitution T C missense_variant R337G 1009A>G BRCA-US 4 153247265 153247265 single base substitution T C missense_variant R395G 1183A>G BRCA-US 4 153247265 153247265 single base substitution T C missense_variant R433G 1297A>G BRCA-US 4 153247265 153247265 single base substitution T C missense_variant R513G 1537A>G BRCA-US 4 153247265 153247265 single base substitution T C upstream_gene_variant BRCA-US 4 153247366 153247366 single base substitution C T downstream_gene_variant BRCA-US 4 153247366 153247366 single base substitution C T exon_variant BRCA-US 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A BRCA-US 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A BRCA-US 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A BRCA-US 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A BRCA-US 4 153247366 153247366 single base substitution C T upstream_gene_variant BRCA-US 4 153249385 153249385 single base substitution G A exon_variant BRCA-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T BRCA-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T BRCA-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T BRCA-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T BRCA-US 4 153249385 153249385 single base substitution G A upstream_gene_variant BRCA-US 4 153250865 153250865 single base substitution C G exon_variant BRCA-US 4 153250865 153250865 single base substitution C G missense_variant D223H 667G>C BRCA-US 4 153250865 153250865 single base substitution C G missense_variant D281H 841G>C BRCA-US 4 153250865 153250865 single base substitution C G missense_variant D319H 955G>C BRCA-US 4 153250865 153250865 single base substitution C G missense_variant D399H 1195G>C BRCA-US 4 153250865 153250865 single base substitution C G upstream_gene_variant BRCA-US 4 153250888 153250888 single base substitution C T exon_variant BRCA-US 4 153250888 153250888 single base substitution C T missense_variant G215D 644G>A BRCA-US 4 153250888 153250888 single base substitution C T missense_variant G273D 818G>A BRCA-US 4 153250888 153250888 single base substitution C T missense_variant G311D 932G>A BRCA-US 4 153250888 153250888 single base substitution C T missense_variant G391D 1172G>A BRCA-US 4 153250888 153250888 single base substitution C T upstream_gene_variant BRCA-US 4 153251936 153251936 single base substitution C T exon_variant BRCA-US 4 153251936 153251936 single base substitution C T missense_variant R181K 542G>A BRCA-US 4 153251936 153251936 single base substitution C T missense_variant R239K 716G>A BRCA-US 4 153251936 153251936 single base substitution C T missense_variant R277K 830G>A BRCA-US 4 153251936 153251936 single base substitution C T missense_variant R357K 1070G>A BRCA-US 4 153251936 153251936 single base substitution C T upstream_gene_variant BRCA-US 4 153251995 153251995 single base substitution C T exon_variant BRCA-US 4 153251995 153251995 single base substitution C T synonymous_variant K161K 483G>A BRCA-US 4 153251995 153251995 single base substitution C T synonymous_variant K219K 657G>A BRCA-US 4 153251995 153251995 single base substitution C T synonymous_variant K257K 771G>A BRCA-US 4 153251995 153251995 single base substitution C T synonymous_variant K337K 1011G>A BRCA-US 4 153251995 153251995 single base substitution C T upstream_gene_variant BRCA-US 4 153253808 153253808 deletion of <=200bp G - exon_variant BRCA-US 4 153253808 153253808 deletion of <=200bp G - frameshift_variant R133 BRCA-US 4 153253808 153253808 deletion of <=200bp G - frameshift_variant R191 BRCA-US 4 153253808 153253808 deletion of <=200bp G - frameshift_variant R229 BRCA-US 4 153253808 153253808 deletion of <=200bp G - frameshift_variant R309 BRCA-US 4 153253808 153253808 deletion of <=200bp G - upstream_gene_variant BRCA-US 4 153253831 153253831 single base substitution A G exon_variant BRCA-US 4 153253831 153253831 single base substitution A G missense_variant L125P 374T>C BRCA-US 4 153253831 153253831 single base substitution A G missense_variant L183P 548T>C BRCA-US 4 153253831 153253831 single base substitution A G missense_variant L221P 662T>C BRCA-US 4 153253831 153253831 single base substitution A G missense_variant L301P 902T>C BRCA-US 4 153253831 153253831 single base substitution A G upstream_gene_variant BRCA-US 4 153271249 153271249 single base substitution C G exon_variant BRCA-US 4 153271249 153271249 single base substitution C G missense_variant E177Q 529G>C BRCA-US 4 153271249 153271249 single base substitution C G missense_variant E59Q 175G>C BRCA-US 4 153271249 153271249 single base substitution C G missense_variant E97Q 289G>C BRCA-US 4 153271249 153271249 single base substitution C G upstream_gene_variant BRCA-US 4 153271249 153271249 single base substitution C T exon_variant BRCA-US 4 153271249 153271249 single base substitution C T missense_variant E177K 529G>A BRCA-US 4 153271249 153271249 single base substitution C T missense_variant E59K 175G>A BRCA-US 4 153271249 153271249 single base substitution C T missense_variant E97K 289G>A BRCA-US 4 153271249 153271249 single base substitution C T upstream_gene_variant BRCA-US 4 153332699 153332699 single base substitution G A missense_variant S86L 257C>T BRCA-US 4 153332918 153332918 single base substitution C A missense_variant R13L 38G>T BTCA-JP 4 153245498 153245498 single base substitution C A downstream_gene_variant BTCA-JP 4 153245498 153245498 single base substitution C A exon_variant BTCA-JP 4 153245498 153245498 single base substitution C A missense_variant V389F 1165G>T BTCA-JP 4 153245498 153245498 single base substitution C A missense_variant V447F 1339G>T BTCA-JP 4 153245498 153245498 single base substitution C A missense_variant V485F 1453G>T BTCA-JP 4 153245498 153245498 single base substitution C A missense_variant V565F 1693G>T BTCA-JP 4 153247195 153247195 single base substitution G T downstream_gene_variant BTCA-JP 4 153247195 153247195 single base substitution G T exon_variant BTCA-JP 4 153247195 153247195 single base substitution G T missense_variant T360K 1079C>A BTCA-JP 4 153247195 153247195 single base substitution G T missense_variant T418K 1253C>A BTCA-JP 4 153247195 153247195 single base substitution G T missense_variant T456K 1367C>A BTCA-JP 4 153247195 153247195 single base substitution G T missense_variant T536K 1607C>A BTCA-JP 4 153247195 153247195 single base substitution G T upstream_gene_variant BTCA-JP 4 153247204 153247204 single base substitution C A downstream_gene_variant BTCA-JP 4 153247204 153247204 single base substitution C A exon_variant BTCA-JP 4 153247204 153247204 single base substitution C A missense_variant C357F 1070G>T BTCA-JP 4 153247204 153247204 single base substitution C A missense_variant C415F 1244G>T BTCA-JP 4 153247204 153247204 single base substitution C A missense_variant C453F 1358G>T BTCA-JP 4 153247204 153247204 single base substitution C A missense_variant C533F 1598G>T BTCA-JP 4 153247204 153247204 single base substitution C A upstream_gene_variant BTCA-JP 4 153247252 153247252 single base substitution C T downstream_gene_variant BTCA-JP 4 153247252 153247252 single base substitution C T exon_variant BTCA-JP 4 153247252 153247252 single base substitution C T missense_variant G341E 1022G>A BTCA-JP 4 153247252 153247252 single base substitution C T missense_variant G399E 1196G>A BTCA-JP 4 153247252 153247252 single base substitution C T missense_variant G437E 1310G>A BTCA-JP 4 153247252 153247252 single base substitution C T missense_variant G517E 1550G>A BTCA-JP 4 153247252 153247252 single base substitution C T upstream_gene_variant BTCA-JP 4 153247366 153247366 single base substitution C T downstream_gene_variant BTCA-JP 4 153247366 153247366 single base substitution C T exon_variant BTCA-JP 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A BTCA-JP 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A BTCA-JP 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A BTCA-JP 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A BTCA-JP 4 153247366 153247366 single base substitution C T upstream_gene_variant BTCA-JP 4 153249458 153249458 deletion of <=200bp A - exon_variant BTCA-JP 4 153249458 153249458 deletion of <=200bp A - frameshift_variant D264 BTCA-JP 4 153249458 153249458 deletion of <=200bp A - frameshift_variant D322 BTCA-JP 4 153249458 153249458 deletion of <=200bp A - frameshift_variant D360 BTCA-JP 4 153249458 153249458 deletion of <=200bp A - frameshift_variant D440 BTCA-JP 4 153249458 153249458 deletion of <=200bp A - upstream_gene_variant BTCA-JP 4 153249510 153249510 single base substitution C A exon_variant BTCA-JP 4 153249510 153249510 single base substitution C A missense_variant G247V 740G>T BTCA-JP 4 153249510 153249510 single base substitution C A missense_variant G305V 914G>T BTCA-JP 4 153249510 153249510 single base substitution C A missense_variant G343V 1028G>T BTCA-JP 4 153249510 153249510 single base substitution C A missense_variant G423V 1268G>T BTCA-JP 4 153249510 153249510 single base substitution C A upstream_gene_variant BTCA-JP 4 153273697 153273697 single base substitution C T exon_variant BTCA-JP 4 153273697 153273697 single base substitution C T intron_variant BTCA-JP 4 153273697 153273697 single base substitution C T synonymous_variant G62G 186G>A BTCA-JP 4 153273697 153273697 single base substitution C T upstream_gene_variant BTCA-JP 4 153410465 153410465 deletion of <=200bp T - intron_variant BTCA-JP 4 153457666 153457666 single base substitution A C upstream_gene_variant BTCA-JP 4 153457797 153457797 single base substitution C T upstream_gene_variant CESC-US 4 153244184 153244184 single base substitution C T downstream_gene_variant CESC-US 4 153244184 153244184 single base substitution C T exon_variant CESC-US 4 153244184 153244184 single base substitution C T missense_variant R482Q 1445G>A CESC-US 4 153244184 153244184 single base substitution C T missense_variant R540Q 1619G>A CESC-US 4 153244184 153244184 single base substitution C T missense_variant R578Q 1733G>A CESC-US 4 153244184 153244184 single base substitution C T missense_variant R658Q 1973G>A CESC-US 4 153244185 153244185 single base substitution G T downstream_gene_variant CESC-US 4 153244185 153244185 single base substitution G T exon_variant CESC-US 4 153244185 153244185 single base substitution G T synonymous_variant R482R 1444C>A CESC-US 4 153244185 153244185 single base substitution G T synonymous_variant R540R 1618C>A CESC-US 4 153244185 153244185 single base substitution G T synonymous_variant R578R 1732C>A CESC-US 4 153244185 153244185 single base substitution G T synonymous_variant R658R 1972C>A CESC-US 4 153245393 153245393 single base substitution C G downstream_gene_variant CESC-US 4 153245393 153245393 single base substitution C G exon_variant CESC-US 4 153245393 153245393 single base substitution C G missense_variant D424H 1270G>C CESC-US 4 153245393 153245393 single base substitution C G missense_variant D482H 1444G>C CESC-US 4 153245393 153245393 single base substitution C G missense_variant D520H 1558G>C CESC-US 4 153245393 153245393 single base substitution C G missense_variant D600H 1798G>C CESC-US 4 153245393 153245393 single base substitution C T downstream_gene_variant CESC-US 4 153245393 153245393 single base substitution C T exon_variant CESC-US 4 153245393 153245393 single base substitution C T missense_variant D424N 1270G>A CESC-US 4 153245393 153245393 single base substitution C T missense_variant D482N 1444G>A CESC-US 4 153245393 153245393 single base substitution C T missense_variant D520N 1558G>A CESC-US 4 153245393 153245393 single base substitution C T missense_variant D600N 1798G>A CESC-US 4 153247245 153247245 single base substitution A T downstream_gene_variant CESC-US 4 153247245 153247245 single base substitution A T exon_variant CESC-US 4 153247245 153247245 single base substitution A T stop_gained Y343* 1029T>A CESC-US 4 153247245 153247245 single base substitution A T stop_gained Y401* 1203T>A CESC-US 4 153247245 153247245 single base substitution A T stop_gained Y439* 1317T>A CESC-US 4 153247245 153247245 single base substitution A T stop_gained Y519* 1557T>A CESC-US 4 153247245 153247245 single base substitution A T upstream_gene_variant CESC-US 4 153247280 153247280 single base substitution G A downstream_gene_variant CESC-US 4 153247280 153247280 single base substitution G A exon_variant CESC-US 4 153247280 153247280 single base substitution G A stop_gained Q332* 994C>T CESC-US 4 153247280 153247280 single base substitution G A stop_gained Q390* 1168C>T CESC-US 4 153247280 153247280 single base substitution G A stop_gained Q428* 1282C>T CESC-US 4 153247280 153247280 single base substitution G A stop_gained Q508* 1522C>T CESC-US 4 153247280 153247280 single base substitution G A upstream_gene_variant CESC-US 4 153247289 153247289 single base substitution G A downstream_gene_variant CESC-US 4 153247289 153247289 single base substitution G A exon_variant CESC-US 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T CESC-US 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T CESC-US 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T CESC-US 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T CESC-US 4 153247289 153247289 single base substitution G A upstream_gene_variant CESC-US 4 153247289 153247289 single base substitution G C downstream_gene_variant CESC-US 4 153247289 153247289 single base substitution G C exon_variant CESC-US 4 153247289 153247289 single base substitution G C missense_variant R329G 985C>G CESC-US 4 153247289 153247289 single base substitution G C missense_variant R387G 1159C>G CESC-US 4 153247289 153247289 single base substitution G C missense_variant R425G 1273C>G CESC-US 4 153247289 153247289 single base substitution G C missense_variant R505G 1513C>G CESC-US 4 153247289 153247289 single base substitution G C upstream_gene_variant CESC-US 4 153247304 153247304 single base substitution G C downstream_gene_variant CESC-US 4 153247304 153247304 single base substitution G C exon_variant CESC-US 4 153247304 153247304 single base substitution G C missense_variant H324D 970C>G CESC-US 4 153247304 153247304 single base substitution G C missense_variant H382D 1144C>G CESC-US 4 153247304 153247304 single base substitution G C missense_variant H420D 1258C>G CESC-US 4 153247304 153247304 single base substitution G C missense_variant H500D 1498C>G CESC-US 4 153247304 153247304 single base substitution G C upstream_gene_variant CESC-US 4 153247366 153247366 single base substitution C G downstream_gene_variant CESC-US 4 153247366 153247366 single base substitution C G exon_variant CESC-US 4 153247366 153247366 single base substitution C G missense_variant R303P 908G>C CESC-US 4 153247366 153247366 single base substitution C G missense_variant R361P 1082G>C CESC-US 4 153247366 153247366 single base substitution C G missense_variant R399P 1196G>C CESC-US 4 153247366 153247366 single base substitution C G missense_variant R479P 1436G>C CESC-US 4 153247366 153247366 single base substitution C G upstream_gene_variant CESC-US 4 153247366 153247366 single base substitution C T downstream_gene_variant CESC-US 4 153247366 153247366 single base substitution C T exon_variant CESC-US 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A CESC-US 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A CESC-US 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A CESC-US 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A CESC-US 4 153247366 153247366 single base substitution C T upstream_gene_variant CESC-US 4 153247367 153247367 single base substitution G C downstream_gene_variant CESC-US 4 153247367 153247367 single base substitution G C exon_variant CESC-US 4 153247367 153247367 single base substitution G C missense_variant R303G 907C>G CESC-US 4 153247367 153247367 single base substitution G C missense_variant R361G 1081C>G CESC-US 4 153247367 153247367 single base substitution G C missense_variant R399G 1195C>G CESC-US 4 153247367 153247367 single base substitution G C missense_variant R479G 1435C>G CESC-US 4 153247367 153247367 single base substitution G C upstream_gene_variant CESC-US 4 153249384 153249384 single base substitution C A exon_variant CESC-US 4 153249384 153249384 single base substitution C A missense_variant R289L 866G>T CESC-US 4 153249384 153249384 single base substitution C A missense_variant R347L 1040G>T CESC-US 4 153249384 153249384 single base substitution C A missense_variant R385L 1154G>T CESC-US 4 153249384 153249384 single base substitution C A missense_variant R465L 1394G>T CESC-US 4 153249384 153249384 single base substitution C A upstream_gene_variant CESC-US 4 153249384 153249384 single base substitution C T exon_variant CESC-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A CESC-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A CESC-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A CESC-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A CESC-US 4 153249384 153249384 single base substitution C T upstream_gene_variant CESC-US 4 153249385 153249385 single base substitution G A exon_variant CESC-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T CESC-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T CESC-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T CESC-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T CESC-US 4 153249385 153249385 single base substitution G A upstream_gene_variant CESC-US 4 153251907 153251907 single base substitution G A exon_variant CESC-US 4 153251907 153251907 single base substitution G A stop_gained R191* 571C>T CESC-US 4 153251907 153251907 single base substitution G A stop_gained R249* 745C>T CESC-US 4 153251907 153251907 single base substitution G A stop_gained R287* 859C>T CESC-US 4 153251907 153251907 single base substitution G A stop_gained R367* 1099C>T CESC-US 4 153251907 153251907 single base substitution G A upstream_gene_variant CESC-US 4 153253770 153253770 single base substitution C T exon_variant CESC-US 4 153253770 153253770 single base substitution C T stop_gained W145* 435G>A CESC-US 4 153253770 153253770 single base substitution C T stop_gained W203* 609G>A CESC-US 4 153253770 153253770 single base substitution C T stop_gained W241* 723G>A CESC-US 4 153253770 153253770 single base substitution C T stop_gained W321* 963G>A CESC-US 4 153253770 153253770 single base substitution C T upstream_gene_variant CESC-US 4 153258986 153258986 single base substitution G C missense_variant Q101E 301C>G CESC-US 4 153258986 153258986 single base substitution G C missense_variant Q159E 475C>G CESC-US 4 153258986 153258986 single base substitution G C missense_variant Q197E 589C>G CESC-US 4 153258986 153258986 single base substitution G C missense_variant Q277E 829C>G CESC-US 4 153268138 153268138 single base substitution G A exon_variant CESC-US 4 153268138 153268138 single base substitution G A stop_gained R106* 316C>T CESC-US 4 153268138 153268138 single base substitution G A stop_gained R144* 430C>T CESC-US 4 153268138 153268138 single base substitution G A stop_gained R224* 670C>T CESC-US 4 153268138 153268138 single base substitution G A stop_gained R48* 142C>T CESC-US 4 153410533 153410533 single base substitution A G intron_variant CLLE-ES 4 153249384 153249384 single base substitution C A exon_variant CLLE-ES 4 153249384 153249384 single base substitution C A missense_variant R289L 866G>T CLLE-ES 4 153249384 153249384 single base substitution C A missense_variant R347L 1040G>T CLLE-ES 4 153249384 153249384 single base substitution C A missense_variant R385L 1154G>T CLLE-ES 4 153249384 153249384 single base substitution C A missense_variant R465L 1394G>T CLLE-ES 4 153249384 153249384 single base substitution C A upstream_gene_variant CLLE-ES 4 153249385 153249385 single base substitution G A exon_variant CLLE-ES 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T CLLE-ES 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T CLLE-ES 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T CLLE-ES 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T CLLE-ES 4 153249385 153249385 single base substitution G A upstream_gene_variant CLLE-ES 4 153251907 153251907 single base substitution G A exon_variant CLLE-ES 4 153251907 153251907 single base substitution G A stop_gained R191* 571C>T CLLE-ES 4 153251907 153251907 single base substitution G A stop_gained R249* 745C>T CLLE-ES 4 153251907 153251907 single base substitution G A stop_gained R287* 859C>T CLLE-ES 4 153251907 153251907 single base substitution G A stop_gained R367* 1099C>T CLLE-ES 4 153251907 153251907 single base substitution G A upstream_gene_variant CLLE-ES 4 153263748 153263748 single base substitution C T downstream_gene_variant CLLE-ES 4 153263748 153263748 single base substitution C T intron_variant CLLE-ES 4 153283137 153283137 single base substitution A G intron_variant CLLE-ES 4 153309128 153309128 single base substitution G A intron_variant CLLE-ES 4 153317840 153317840 single base substitution A G intron_variant CLLE-ES 4 153339808 153339808 single base substitution C T intron_variant CLLE-ES 4 153404570 153404570 single base substitution T G intron_variant CLLE-ES 4 153407150 153407150 single base substitution T A intron_variant CLLE-ES 4 153419074 153419075 deletion of <=200bp AT - intron_variant COAD-US 4 153244156 153244156 deletion of <=200bp C - downstream_gene_variant COAD-US 4 153244156 153244156 deletion of <=200bp C - exon_variant COAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G491 COAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G549 COAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G587 COAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G667 COAD-US 4 153244185 153244185 single base substitution G A downstream_gene_variant COAD-US 4 153244185 153244185 single base substitution G A exon_variant COAD-US 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T COAD-US 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T COAD-US 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T COAD-US 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T COAD-US 4 153244280 153244280 single base substitution G T downstream_gene_variant COAD-US 4 153244280 153244280 single base substitution G T exon_variant COAD-US 4 153244280 153244280 single base substitution G T missense_variant A450D 1349C>A COAD-US 4 153244280 153244280 single base substitution G T missense_variant A508D 1523C>A COAD-US 4 153244280 153244280 single base substitution G T missense_variant A546D 1637C>A COAD-US 4 153244280 153244280 single base substitution G T missense_variant A626D 1877C>A COAD-US 4 153245343 153245343 single base substitution T A downstream_gene_variant COAD-US 4 153245343 153245343 single base substitution T A exon_variant COAD-US 4 153245343 153245343 single base substitution T A synonymous_variant T440T 1320A>T COAD-US 4 153245343 153245343 single base substitution T A synonymous_variant T498T 1494A>T COAD-US 4 153245343 153245343 single base substitution T A synonymous_variant T536T 1608A>T COAD-US 4 153245343 153245343 single base substitution T A synonymous_variant T616T 1848A>T COAD-US 4 153245446 153245446 single base substitution G A downstream_gene_variant COAD-US 4 153245446 153245446 single base substitution G A exon_variant COAD-US 4 153245446 153245446 single base substitution G A missense_variant S406L 1217C>T COAD-US 4 153245446 153245446 single base substitution G A missense_variant S464L 1391C>T COAD-US 4 153245446 153245446 single base substitution G A missense_variant S502L 1505C>T COAD-US 4 153245446 153245446 single base substitution G A missense_variant S582L 1745C>T COAD-US 4 153247196 153247196 single base substitution T G downstream_gene_variant COAD-US 4 153247196 153247196 single base substitution T G exon_variant COAD-US 4 153247196 153247196 single base substitution T G missense_variant T360P 1078A>C COAD-US 4 153247196 153247196 single base substitution T G missense_variant T418P 1252A>C COAD-US 4 153247196 153247196 single base substitution T G missense_variant T456P 1366A>C COAD-US 4 153247196 153247196 single base substitution T G missense_variant T536P 1606A>C COAD-US 4 153247196 153247196 single base substitution T G upstream_gene_variant COAD-US 4 153247289 153247289 single base substitution G A downstream_gene_variant COAD-US 4 153247289 153247289 single base substitution G A exon_variant COAD-US 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T COAD-US 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T COAD-US 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T COAD-US 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T COAD-US 4 153247289 153247289 single base substitution G A upstream_gene_variant COAD-US 4 153247367 153247367 single base substitution G A downstream_gene_variant COAD-US 4 153247367 153247367 single base substitution G A exon_variant COAD-US 4 153247367 153247367 single base substitution G A stop_gained R303* 907C>T COAD-US 4 153247367 153247367 single base substitution G A stop_gained R361* 1081C>T COAD-US 4 153247367 153247367 single base substitution G A stop_gained R399* 1195C>T COAD-US 4 153247367 153247367 single base substitution G A stop_gained R479* 1435C>T COAD-US 4 153247367 153247367 single base substitution G A upstream_gene_variant COAD-US 4 153247367 153247367 single base substitution G C downstream_gene_variant COAD-US 4 153247367 153247367 single base substitution G C exon_variant COAD-US 4 153247367 153247367 single base substitution G C missense_variant R303G 907C>G COAD-US 4 153247367 153247367 single base substitution G C missense_variant R361G 1081C>G COAD-US 4 153247367 153247367 single base substitution G C missense_variant R399G 1195C>G COAD-US 4 153247367 153247367 single base substitution G C missense_variant R479G 1435C>G COAD-US 4 153247367 153247367 single base substitution G C upstream_gene_variant COAD-US 4 153249384 153249384 single base substitution C T exon_variant COAD-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A COAD-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A COAD-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A COAD-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A COAD-US 4 153249384 153249384 single base substitution C T upstream_gene_variant COAD-US 4 153249385 153249385 single base substitution G A exon_variant COAD-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T COAD-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T COAD-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T COAD-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T COAD-US 4 153249385 153249385 single base substitution G A upstream_gene_variant COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC exon_variant COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC frameshift_variant H244HVG? COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC frameshift_variant H302HVG? COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC frameshift_variant H340HVG? COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC frameshift_variant H420HVG? COAD-US 4 153249518 153249518 insertion of <=200bp - TGTCCCAC upstream_gene_variant COAD-US 4 153250882 153250882 single base substitution C T exon_variant COAD-US 4 153250882 153250882 single base substitution C T missense_variant R217Q 650G>A COAD-US 4 153250882 153250882 single base substitution C T missense_variant R275Q 824G>A COAD-US 4 153250882 153250882 single base substitution C T missense_variant R313Q 938G>A COAD-US 4 153250882 153250882 single base substitution C T missense_variant R393Q 1178G>A COAD-US 4 153250882 153250882 single base substitution C T upstream_gene_variant COAD-US 4 153250898 153250898 insertion of <=200bp - T exon_variant COAD-US 4 153250898 153250898 insertion of <=200bp - T frameshift_variant Q212Q? COAD-US 4 153250898 153250898 insertion of <=200bp - T frameshift_variant Q270Q? COAD-US 4 153250898 153250898 insertion of <=200bp - T frameshift_variant Q308Q? COAD-US 4 153250898 153250898 insertion of <=200bp - T frameshift_variant Q388Q? COAD-US 4 153250898 153250898 insertion of <=200bp - T upstream_gene_variant COAD-US 4 153251907 153251907 single base substitution G A exon_variant COAD-US 4 153251907 153251907 single base substitution G A stop_gained R191* 571C>T COAD-US 4 153251907 153251907 single base substitution G A stop_gained R249* 745C>T COAD-US 4 153251907 153251907 single base substitution G A stop_gained R287* 859C>T COAD-US 4 153251907 153251907 single base substitution G A stop_gained R367* 1099C>T COAD-US 4 153251907 153251907 single base substitution G A upstream_gene_variant COAD-US 4 153273739 153273739 deletion of <=200bp T - exon_variant COAD-US 4 153273739 153273739 deletion of <=200bp T - frameshift_variant K48 COAD-US 4 153273739 153273739 deletion of <=200bp T - intron_variant COAD-US 4 153273739 153273739 deletion of <=200bp T - upstream_gene_variant COAD-US 4 153303407 153303407 single base substitution A G intron_variant COAD-US 4 153303407 153303407 single base substitution A G synonymous_variant H27H 81T>C COAD-US 4 153332679 153332679 single base substitution C A stop_gained G93* 277G>T COAD-US 4 153332841 153332847 deletion of <=200bp CCTCTAC - frameshift_variant VEE37 COAD-US 4 153332915 153332915 single base substitution C T missense_variant R14Q 41G>A COCA-CN 4 153244092 153244092 single base substitution G A downstream_gene_variant COCA-CN 4 153244092 153244092 single base substitution G A exon_variant COCA-CN 4 153244092 153244092 single base substitution G A missense_variant R513W 1537C>T COCA-CN 4 153244092 153244092 single base substitution G A missense_variant R571W 1711C>T COCA-CN 4 153244092 153244092 single base substitution G A missense_variant R609W 1825C>T COCA-CN 4 153244092 153244092 single base substitution G A missense_variant R689W 2065C>T COCA-CN 4 153244185 153244185 single base substitution G A downstream_gene_variant COCA-CN 4 153244185 153244185 single base substitution G A exon_variant COCA-CN 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T COCA-CN 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T COCA-CN 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T COCA-CN 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T COCA-CN 4 153244194 153244194 single base substitution C A downstream_gene_variant COCA-CN 4 153244194 153244194 single base substitution C A exon_variant COCA-CN 4 153244194 153244194 single base substitution C A stop_gained E479* 1435G>T COCA-CN 4 153244194 153244194 single base substitution C A stop_gained E537* 1609G>T COCA-CN 4 153244194 153244194 single base substitution C A stop_gained E575* 1723G>T COCA-CN 4 153244194 153244194 single base substitution C A stop_gained E655* 1963G>T COCA-CN 4 153245339 153245339 single base substitution G A downstream_gene_variant COCA-CN 4 153245339 153245339 single base substitution G A exon_variant COCA-CN 4 153245339 153245339 single base substitution G A stop_gained Q442* 1324C>T COCA-CN 4 153245339 153245339 single base substitution G A stop_gained Q500* 1498C>T COCA-CN 4 153245339 153245339 single base substitution G A stop_gained Q538* 1612C>T COCA-CN 4 153245339 153245339 single base substitution G A stop_gained Q618* 1852C>T COCA-CN 4 153245374 153245374 single base substitution C A downstream_gene_variant COCA-CN 4 153245374 153245374 single base substitution C A exon_variant COCA-CN 4 153245374 153245374 single base substitution C A missense_variant W430L 1289G>T COCA-CN 4 153245374 153245374 single base substitution C A missense_variant W488L 1463G>T COCA-CN 4 153245374 153245374 single base substitution C A missense_variant W526L 1577G>T COCA-CN 4 153245374 153245374 single base substitution C A missense_variant W606L 1817G>T COCA-CN 4 153245380 153245380 single base substitution T G downstream_gene_variant COCA-CN 4 153245380 153245380 single base substitution T G exon_variant COCA-CN 4 153245380 153245380 single base substitution T G missense_variant K428T 1283A>C COCA-CN 4 153245380 153245380 single base substitution T G missense_variant K486T 1457A>C COCA-CN 4 153245380 153245380 single base substitution T G missense_variant K524T 1571A>C COCA-CN 4 153245380 153245380 single base substitution T G missense_variant K604T 1811A>C COCA-CN 4 153245446 153245446 single base substitution G A downstream_gene_variant COCA-CN 4 153245446 153245446 single base substitution G A exon_variant COCA-CN 4 153245446 153245446 single base substitution G A missense_variant S406L 1217C>T COCA-CN 4 153245446 153245446 single base substitution G A missense_variant S464L 1391C>T COCA-CN 4 153245446 153245446 single base substitution G A missense_variant S502L 1505C>T COCA-CN 4 153245446 153245446 single base substitution G A missense_variant S582L 1745C>T COCA-CN 4 153247283 153247283 single base substitution C A downstream_gene_variant COCA-CN 4 153247283 153247283 single base substitution C A exon_variant COCA-CN 4 153247283 153247283 single base substitution C A missense_variant V331F 991G>T COCA-CN 4 153247283 153247283 single base substitution C A missense_variant V389F 1165G>T COCA-CN 4 153247283 153247283 single base substitution C A missense_variant V427F 1279G>T COCA-CN 4 153247283 153247283 single base substitution C A missense_variant V507F 1519G>T COCA-CN 4 153247283 153247283 single base substitution C A upstream_gene_variant COCA-CN 4 153247288 153247288 single base substitution C T downstream_gene_variant COCA-CN 4 153247288 153247288 single base substitution C T exon_variant COCA-CN 4 153247288 153247288 single base substitution C T missense_variant R329H 986G>A COCA-CN 4 153247288 153247288 single base substitution C T missense_variant R387H 1160G>A COCA-CN 4 153247288 153247288 single base substitution C T missense_variant R425H 1274G>A COCA-CN 4 153247288 153247288 single base substitution C T missense_variant R505H 1514G>A COCA-CN 4 153247288 153247288 single base substitution C T upstream_gene_variant COCA-CN 4 153247289 153247289 single base substitution G A downstream_gene_variant COCA-CN 4 153247289 153247289 single base substitution G A exon_variant COCA-CN 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T COCA-CN 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T COCA-CN 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T COCA-CN 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T COCA-CN 4 153247289 153247289 single base substitution G A upstream_gene_variant COCA-CN 4 153247366 153247366 single base substitution C T downstream_gene_variant COCA-CN 4 153247366 153247366 single base substitution C T exon_variant COCA-CN 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A COCA-CN 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A COCA-CN 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A COCA-CN 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A COCA-CN 4 153247366 153247366 single base substitution C T upstream_gene_variant COCA-CN 4 153247373 153247373 single base substitution C T downstream_gene_variant COCA-CN 4 153247373 153247373 single base substitution C T exon_variant COCA-CN 4 153247373 153247373 single base substitution C T missense_variant G301S 901G>A COCA-CN 4 153247373 153247373 single base substitution C T missense_variant G359S 1075G>A COCA-CN 4 153247373 153247373 single base substitution C T missense_variant G397S 1189G>A COCA-CN 4 153247373 153247373 single base substitution C T missense_variant G477S 1429G>A COCA-CN 4 153247373 153247373 single base substitution C T upstream_gene_variant COCA-CN 4 153247419 153247419 single base substitution A G intron_variant COCA-CN 4 153247419 153247419 single base substitution A G upstream_gene_variant COCA-CN 4 153249384 153249384 single base substitution C T exon_variant COCA-CN 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A COCA-CN 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A COCA-CN 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A COCA-CN 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A COCA-CN 4 153249384 153249384 single base substitution C T upstream_gene_variant COCA-CN 4 153249385 153249385 single base substitution G A exon_variant COCA-CN 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T COCA-CN 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T COCA-CN 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T COCA-CN 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T COCA-CN 4 153249385 153249385 single base substitution G A upstream_gene_variant COCA-CN 4 153249576 153249576 single base substitution G T exon_variant COCA-CN 4 153249576 153249576 single base substitution G T intron_variant COCA-CN 4 153249576 153249576 single base substitution G T upstream_gene_variant COCA-CN 4 153250985 153250985 single base substitution C A intron_variant COCA-CN 4 153250985 153250985 single base substitution C A upstream_gene_variant COCA-CN 4 153258982 153258982 single base substitution C T missense_variant R102Q 305G>A COCA-CN 4 153258982 153258982 single base substitution C T missense_variant R160Q 479G>A COCA-CN 4 153258982 153258982 single base substitution C T missense_variant R198Q 593G>A COCA-CN 4 153258982 153258982 single base substitution C T missense_variant R278Q 833G>A COCA-CN 4 153258983 153258983 single base substitution G A stop_gained R102* 304C>T COCA-CN 4 153258983 153258983 single base substitution G A stop_gained R160* 478C>T COCA-CN 4 153258983 153258983 single base substitution G A stop_gained R198* 592C>T COCA-CN 4 153258983 153258983 single base substitution G A stop_gained R278* 832C>T COCA-CN 4 153268221 153268221 single base substitution G A missense_variant T116I 347C>T COCA-CN 4 153268221 153268221 single base substitution G A missense_variant T196I 587C>T COCA-CN 4 153268221 153268221 single base substitution G A missense_variant T20I 59C>T COCA-CN 4 153268221 153268221 single base substitution G A missense_variant T78I 233C>T COCA-CN 4 153268221 153268221 single base substitution G A splice_region_variant COCA-CN 4 153268312 153268312 single base substitution C A intron_variant COCA-CN 4 153271193 153271193 single base substitution C A splice_donor_variant COCA-CN 4 153271193 153271193 single base substitution C A upstream_gene_variant COCA-CN 4 153275915 153275915 single base substitution A G intron_variant COCA-CN 4 153275915 153275915 single base substitution A G upstream_gene_variant COCA-CN 4 153303361 153303361 single base substitution G A intron_variant COCA-CN 4 153303361 153303361 single base substitution G A missense_variant L43F 127C>T COCA-CN 4 153332524 153332524 single base substitution C T synonymous_variant T144T 432G>A COCA-CN 4 153332915 153332915 single base substitution C T missense_variant R14Q 41G>A COCA-CN 4 153332921 153332921 single base substitution C A missense_variant R12I 35G>T COCA-CN 4 153383746 153383746 single base substitution C T intron_variant COCA-CN 4 153440475 153440475 single base substitution G T intron_variant EOPC-DE 4 153337212 153337212 single base substitution G A intron_variant EOPC-DE 4 153337212 153337212 single base substitution G A upstream_gene_variant EOPC-DE 4 153358844 153358844 single base substitution C T intron_variant EOPC-DE 4 153413820 153413820 single base substitution G A intron_variant EOPC-DE 4 153449599 153449599 single base substitution T C downstream_gene_variant EOPC-DE 4 153449599 153449599 single base substitution T C intron_variant ESAD-UK 4 153237422 153237422 single base substitution A G downstream_gene_variant ESAD-UK 4 153240582 153240582 single base substitution G A downstream_gene_variant ESAD-UK 4 153241205 153241205 single base substitution C T downstream_gene_variant ESAD-UK 4 153242265 153242265 single base substitution C T downstream_gene_variant ESAD-UK 4 153243539 153243539 single base substitution T A 3_prime_UTR_variant ESAD-UK 4 153243539 153243539 single base substitution T A downstream_gene_variant ESAD-UK 4 153244157 153244157 single base substitution C G downstream_gene_variant ESAD-UK 4 153244157 153244157 single base substitution C G exon_variant ESAD-UK 4 153244157 153244157 single base substitution C G missense_variant G491A 1472G>C ESAD-UK 4 153244157 153244157 single base substitution C G missense_variant G549A 1646G>C ESAD-UK 4 153244157 153244157 single base substitution C G missense_variant G587A 1760G>C ESAD-UK 4 153244157 153244157 single base substitution C G missense_variant G667A 2000G>C ESAD-UK 4 153244185 153244185 single base substitution G A downstream_gene_variant ESAD-UK 4 153244185 153244185 single base substitution G A exon_variant ESAD-UK 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T ESAD-UK 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T ESAD-UK 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T ESAD-UK 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T ESAD-UK 4 153245524 153245524 single base substitution C T downstream_gene_variant ESAD-UK 4 153245524 153245524 single base substitution C T exon_variant ESAD-UK 4 153245524 153245524 single base substitution C T missense_variant S380N 1139G>A ESAD-UK 4 153245524 153245524 single base substitution C T missense_variant S438N 1313G>A ESAD-UK 4 153245524 153245524 single base substitution C T missense_variant S476N 1427G>A ESAD-UK 4 153245524 153245524 single base substitution C T missense_variant S556N 1667G>A ESAD-UK 4 153247153 153247153 single base substitution C T downstream_gene_variant ESAD-UK 4 153247153 153247153 single base substitution C T exon_variant ESAD-UK 4 153247153 153247153 single base substitution C T splice_region_variant ESAD-UK 4 153247153 153247153 single base substitution C T upstream_gene_variant ESAD-UK 4 153247289 153247289 single base substitution G A downstream_gene_variant ESAD-UK 4 153247289 153247289 single base substitution G A exon_variant ESAD-UK 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T ESAD-UK 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T ESAD-UK 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T ESAD-UK 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T ESAD-UK 4 153247289 153247289 single base substitution G A upstream_gene_variant ESAD-UK 4 153247367 153247367 single base substitution G C downstream_gene_variant ESAD-UK 4 153247367 153247367 single base substitution G C exon_variant ESAD-UK 4 153247367 153247367 single base substitution G C missense_variant R303G 907C>G ESAD-UK 4 153247367 153247367 single base substitution G C missense_variant R361G 1081C>G ESAD-UK 4 153247367 153247367 single base substitution G C missense_variant R399G 1195C>G ESAD-UK 4 153247367 153247367 single base substitution G C missense_variant R479G 1435C>G ESAD-UK 4 153247367 153247367 single base substitution G C upstream_gene_variant ESAD-UK 4 153247913 153247913 single base substitution A T intron_variant ESAD-UK 4 153247913 153247913 single base substitution A T upstream_gene_variant ESAD-UK 4 153248860 153248860 single base substitution T C intron_variant ESAD-UK 4 153248860 153248860 single base substitution T C upstream_gene_variant ESAD-UK 4 153249385 153249385 single base substitution G A exon_variant ESAD-UK 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T ESAD-UK 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T ESAD-UK 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T ESAD-UK 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T ESAD-UK 4 153249385 153249385 single base substitution G A upstream_gene_variant ESAD-UK 4 153251301 153251301 single base substitution C T intron_variant ESAD-UK 4 153251301 153251301 single base substitution C T upstream_gene_variant ESAD-UK 4 153251486 153251486 single base substitution C T intron_variant ESAD-UK 4 153251486 153251486 single base substitution C T upstream_gene_variant ESAD-UK 4 153254340 153254340 single base substitution T A intron_variant ESAD-UK 4 153254340 153254340 single base substitution T A upstream_gene_variant ESAD-UK 4 153254584 153254584 deletion of <=200bp T - intron_variant ESAD-UK 4 153254584 153254584 deletion of <=200bp T - upstream_gene_variant ESAD-UK 4 153257232 153257232 single base substitution T C intron_variant ESAD-UK 4 153257232 153257232 single base substitution T C upstream_gene_variant ESAD-UK 4 153258317 153258317 single base substitution A C intron_variant ESAD-UK 4 153258317 153258317 single base substitution A C upstream_gene_variant ESAD-UK 4 153258333 153258333 single base substitution T G intron_variant ESAD-UK 4 153258333 153258333 single base substitution T G upstream_gene_variant ESAD-UK 4 153258659 153258659 insertion of <=200bp - A intron_variant ESAD-UK 4 153258659 153258659 insertion of <=200bp - A upstream_gene_variant ESAD-UK 4 153260168 153260168 single base substitution G T intron_variant ESAD-UK 4 153261562 153261562 single base substitution T C intron_variant ESAD-UK 4 153262808 153262808 single base substitution T C intron_variant ESAD-UK 4 153264510 153264510 single base substitution A T downstream_gene_variant ESAD-UK 4 153264510 153264510 single base substitution A T intron_variant ESAD-UK 4 153266702 153266702 single base substitution C T downstream_gene_variant ESAD-UK 4 153266702 153266702 single base substitution C T intron_variant ESAD-UK 4 153266930 153266930 single base substitution T C downstream_gene_variant ESAD-UK 4 153266930 153266930 single base substitution T C intron_variant ESAD-UK 4 153267215 153267215 single base substitution G A downstream_gene_variant ESAD-UK 4 153267215 153267215 single base substitution G A intron_variant ESAD-UK 4 153267982 153267982 single base substitution T C exon_variant ESAD-UK 4 153267982 153267982 single base substitution T C intron_variant ESAD-UK 4 153268138 153268138 single base substitution G A exon_variant ESAD-UK 4 153268138 153268138 single base substitution G A stop_gained R106* 316C>T ESAD-UK 4 153268138 153268138 single base substitution G A stop_gained R144* 430C>T ESAD-UK 4 153268138 153268138 single base substitution G A stop_gained R224* 670C>T ESAD-UK 4 153268138 153268138 single base substitution G A stop_gained R48* 142C>T ESAD-UK 4 153269188 153269188 single base substitution C T intron_variant ESAD-UK 4 153269499 153269499 single base substitution G C intron_variant ESAD-UK 4 153273931 153273931 single base substitution A G 5_prime_UTR_variant ESAD-UK 4 153273931 153273931 single base substitution A G intron_variant ESAD-UK 4 153273931 153273931 single base substitution A G upstream_gene_variant ESAD-UK 4 153277208 153277208 single base substitution T A intron_variant ESAD-UK 4 153277208 153277208 single base substitution T A upstream_gene_variant ESAD-UK 4 153278196 153278196 single base substitution A G intron_variant ESAD-UK 4 153278196 153278196 single base substitution A G upstream_gene_variant ESAD-UK 4 153278789 153278789 single base substitution G A intron_variant ESAD-UK 4 153278789 153278789 single base substitution G A upstream_gene_variant ESAD-UK 4 153285626 153285626 single base substitution G C intron_variant ESAD-UK 4 153286537 153286537 single base substitution T C intron_variant ESAD-UK 4 153286678 153286678 single base substitution G T intron_variant ESAD-UK 4 153290282 153290282 single base substitution C T intron_variant ESAD-UK 4 153290915 153290915 single base substitution C T intron_variant ESAD-UK 4 153295550 153295553 deletion of <=200bp TAAG - intron_variant ESAD-UK 4 153295817 153295817 single base substitution A T intron_variant ESAD-UK 4 153298304 153298304 single base substitution T C intron_variant ESAD-UK 4 153298735 153298735 single base substitution C G intron_variant ESAD-UK 4 153304035 153304035 single base substitution A T intron_variant ESAD-UK 4 153304035 153304035 single base substitution A T upstream_gene_variant ESAD-UK 4 153308957 153308957 single base substitution T C intron_variant ESAD-UK 4 153309006 153309006 single base substitution G A intron_variant ESAD-UK 4 153310911 153310911 deletion of <=200bp A - intron_variant ESAD-UK 4 153310911 153310911 insertion of <=200bp - A intron_variant ESAD-UK 4 153312460 153312460 single base substitution G T intron_variant ESAD-UK 4 153317166 153317166 single base substitution A C intron_variant ESAD-UK 4 153319921 153319921 single base substitution T A intron_variant ESAD-UK 4 153320737 153320737 deletion of <=200bp A - intron_variant ESAD-UK 4 153321095 153321095 single base substitution C T intron_variant ESAD-UK 4 153324756 153324756 single base substitution C G intron_variant ESAD-UK 4 153329501 153329501 single base substitution T A downstream_gene_variant ESAD-UK 4 153329501 153329501 single base substitution T A intron_variant ESAD-UK 4 153333290 153333290 single base substitution C A intron_variant ESAD-UK 4 153333290 153333290 single base substitution C A upstream_gene_variant ESAD-UK 4 153333751 153333751 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 4 153333751 153333751 single base substitution G C intron_variant ESAD-UK 4 153333751 153333751 single base substitution G C upstream_gene_variant ESAD-UK 4 153338542 153338542 single base substitution C T intron_variant ESAD-UK 4 153338542 153338542 single base substitution C T upstream_gene_variant ESAD-UK 4 153339114 153339114 single base substitution G C intron_variant ESAD-UK 4 153339903 153339903 single base substitution G A intron_variant ESAD-UK 4 153340705 153340705 deletion of <=200bp A - intron_variant ESAD-UK 4 153342279 153342279 single base substitution C A intron_variant ESAD-UK 4 153342395 153342395 single base substitution T A intron_variant ESAD-UK 4 153342458 153342458 single base substitution G C intron_variant ESAD-UK 4 153343238 153343238 single base substitution A T intron_variant ESAD-UK 4 153343948 153343948 single base substitution C G intron_variant ESAD-UK 4 153346112 153346112 single base substitution T A intron_variant ESAD-UK 4 153347154 153347154 single base substitution A T intron_variant ESAD-UK 4 153356120 153356120 single base substitution C A intron_variant ESAD-UK 4 153361540 153361540 single base substitution T A intron_variant ESAD-UK 4 153366275 153366275 single base substitution G A intron_variant ESAD-UK 4 153367623 153367623 single base substitution T C intron_variant ESAD-UK 4 153368333 153368333 insertion of <=200bp - CA intron_variant ESAD-UK 4 153370231 153370231 single base substitution G C intron_variant ESAD-UK 4 153371361 153371361 single base substitution A C intron_variant ESAD-UK 4 153375414 153375416 deletion of <=200bp CTT - intron_variant ESAD-UK 4 153375880 153375880 insertion of <=200bp - A intron_variant ESAD-UK 4 153381310 153381310 single base substitution G A intron_variant ESAD-UK 4 153388867 153388867 single base substitution C T intron_variant ESAD-UK 4 153390540 153390540 single base substitution G T intron_variant ESAD-UK 4 153390585 153390585 single base substitution T C intron_variant ESAD-UK 4 153390736 153390736 single base substitution G C intron_variant ESAD-UK 4 153393098 153393098 single base substitution G A intron_variant ESAD-UK 4 153393734 153393734 insertion of <=200bp - A intron_variant ESAD-UK 4 153395946 153395946 single base substitution T C intron_variant ESAD-UK 4 153398841 153398841 single base substitution T C intron_variant ESAD-UK 4 153400965 153400965 single base substitution G A intron_variant ESAD-UK 4 153401419 153401419 single base substitution G C intron_variant ESAD-UK 4 153403938 153403938 single base substitution A T intron_variant ESAD-UK 4 153405607 153405607 deletion of <=200bp T - intron_variant ESAD-UK 4 153412129 153412130 deletion of <=200bp AG - intron_variant ESAD-UK 4 153418127 153418127 single base substitution A T intron_variant ESAD-UK 4 153418803 153418803 insertion of <=200bp - A intron_variant ESAD-UK 4 153420128 153420128 single base substitution T A intron_variant ESAD-UK 4 153420510 153420510 single base substitution G A intron_variant ESAD-UK 4 153421833 153421833 single base substitution T C intron_variant ESAD-UK 4 153422559 153422559 single base substitution A C intron_variant ESAD-UK 4 153427330 153427330 single base substitution C T intron_variant ESAD-UK 4 153429030 153429030 single base substitution T A intron_variant ESAD-UK 4 153429192 153429192 single base substitution A G intron_variant ESAD-UK 4 153429403 153429403 deletion of <=200bp A - intron_variant ESAD-UK 4 153433128 153433128 single base substitution C G intron_variant ESAD-UK 4 153434062 153434062 single base substitution G A intron_variant ESAD-UK 4 153435889 153435889 deletion of <=200bp G - intron_variant ESAD-UK 4 153440472 153440472 insertion of <=200bp - AAAG intron_variant ESAD-UK 4 153445224 153445224 single base substitution G C intron_variant ESAD-UK 4 153445438 153445438 single base substitution C T intron_variant ESAD-UK 4 153449769 153449769 single base substitution A G downstream_gene_variant ESAD-UK 4 153449769 153449769 single base substitution A G intron_variant ESAD-UK 4 153452213 153452213 insertion of <=200bp - AC intron_variant ESAD-UK 4 153455634 153455634 single base substitution T C intron_variant ESAD-UK 4 153456043 153456043 single base substitution G A intron_variant ESAD-UK 4 153456970 153456975 deletion of <=200bp GGCTCG - 5_prime_UTR_variant ESAD-UK 4 153456970 153456975 deletion of <=200bp GGCTCG - upstream_gene_variant ESAD-UK 4 153457848 153457848 single base substitution A G upstream_gene_variant ESAD-UK 4 153458999 153458999 single base substitution T C upstream_gene_variant ESAD-UK 4 153460152 153460152 single base substitution T C upstream_gene_variant ESAD-UK 4 153462161 153462161 single base substitution T G upstream_gene_variant ESCA-CN 4 153244303 153244303 single base substitution T C downstream_gene_variant ESCA-CN 4 153244303 153244303 single base substitution T C exon_variant ESCA-CN 4 153244303 153244303 single base substitution T C splice_acceptor_variant ESCA-CN 4 153247175 153247175 single base substitution T C downstream_gene_variant ESCA-CN 4 153247175 153247175 single base substitution T C exon_variant ESCA-CN 4 153247175 153247175 single base substitution T C missense_variant R367G 1099A>G ESCA-CN 4 153247175 153247175 single base substitution T C missense_variant R425G 1273A>G ESCA-CN 4 153247175 153247175 single base substitution T C missense_variant R463G 1387A>G ESCA-CN 4 153247175 153247175 single base substitution T C missense_variant R543G 1627A>G ESCA-CN 4 153247175 153247175 single base substitution T C upstream_gene_variant ESCA-CN 4 153247289 153247289 single base substitution G C downstream_gene_variant ESCA-CN 4 153247289 153247289 single base substitution G C exon_variant ESCA-CN 4 153247289 153247289 single base substitution G C missense_variant R329G 985C>G ESCA-CN 4 153247289 153247289 single base substitution G C missense_variant R387G 1159C>G ESCA-CN 4 153247289 153247289 single base substitution G C missense_variant R425G 1273C>G ESCA-CN 4 153247289 153247289 single base substitution G C missense_variant R505G 1513C>G ESCA-CN 4 153247289 153247289 single base substitution G C upstream_gene_variant ESCA-CN 4 153247366 153247366 single base substitution C T downstream_gene_variant ESCA-CN 4 153247366 153247366 single base substitution C T exon_variant ESCA-CN 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A ESCA-CN 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A ESCA-CN 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A ESCA-CN 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A ESCA-CN 4 153247366 153247366 single base substitution C T upstream_gene_variant ESCA-CN 4 153249384 153249384 single base substitution C T exon_variant ESCA-CN 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A ESCA-CN 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A ESCA-CN 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A ESCA-CN 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A ESCA-CN 4 153249384 153249384 single base substitution C T upstream_gene_variant ESCA-CN 4 153249468 153249468 single base substitution C T exon_variant ESCA-CN 4 153249468 153249468 single base substitution C T missense_variant G261E 782G>A ESCA-CN 4 153249468 153249468 single base substitution C T missense_variant G319E 956G>A ESCA-CN 4 153249468 153249468 single base substitution C T missense_variant G357E 1070G>A ESCA-CN 4 153249468 153249468 single base substitution C T missense_variant G437E 1310G>A ESCA-CN 4 153249468 153249468 single base substitution C T upstream_gene_variant ESCA-CN 4 153250907 153250907 single base substitution T G exon_variant ESCA-CN 4 153250907 153250907 single base substitution T G missense_variant T209P 625A>C ESCA-CN 4 153250907 153250907 single base substitution T G missense_variant T267P 799A>C ESCA-CN 4 153250907 153250907 single base substitution T G missense_variant T305P 913A>C ESCA-CN 4 153250907 153250907 single base substitution T G missense_variant T385P 1153A>C ESCA-CN 4 153250907 153250907 single base substitution T G upstream_gene_variant GBM-US 4 153244185 153244185 single base substitution G A downstream_gene_variant GBM-US 4 153244185 153244185 single base substitution G A exon_variant GBM-US 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T GBM-US 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T GBM-US 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T GBM-US 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T KIRC-US 4 153244135 153244135 single base substitution C G downstream_gene_variant KIRC-US 4 153244135 153244135 single base substitution C G exon_variant KIRC-US 4 153244135 153244135 single base substitution C G synonymous_variant R498R 1494G>C KIRC-US 4 153244135 153244135 single base substitution C G synonymous_variant R556R 1668G>C KIRC-US 4 153244135 153244135 single base substitution C G synonymous_variant R594R 1782G>C KIRC-US 4 153244135 153244135 single base substitution C G synonymous_variant R674R 2022G>C KIRC-US 4 153332528 153332528 single base substitution A T missense_variant V143D 428T>A KIRP-US 4 153250883 153250883 deletion of <=200bp G - exon_variant KIRP-US 4 153250883 153250883 deletion of <=200bp G - frameshift_variant R217 KIRP-US 4 153250883 153250883 deletion of <=200bp G - frameshift_variant R275 KIRP-US 4 153250883 153250883 deletion of <=200bp G - frameshift_variant R313 KIRP-US 4 153250883 153250883 deletion of <=200bp G - frameshift_variant R393 KIRP-US 4 153250883 153250883 deletion of <=200bp G - upstream_gene_variant KIRP-US 4 153268165 153268165 single base substitution C T exon_variant KIRP-US 4 153268165 153268165 single base substitution C T missense_variant A135T 403G>A KIRP-US 4 153268165 153268165 single base substitution C T missense_variant A215T 643G>A KIRP-US 4 153268165 153268165 single base substitution C T missense_variant A39T 115G>A KIRP-US 4 153268165 153268165 single base substitution C T missense_variant A97T 289G>A LAML-KR 4 153259575 153259575 single base substitution C T intron_variant LAML-KR 4 153287888 153287888 single base substitution A G intron_variant LGG-US 4 153244137 153244137 single base substitution G A downstream_gene_variant LGG-US 4 153244137 153244137 single base substitution G A exon_variant LGG-US 4 153244137 153244137 single base substitution G A missense_variant R498W 1492C>T LGG-US 4 153244137 153244137 single base substitution G A missense_variant R556W 1666C>T LGG-US 4 153244137 153244137 single base substitution G A missense_variant R594W 1780C>T LGG-US 4 153244137 153244137 single base substitution G A missense_variant R674W 2020C>T LICA-CN 4 153249515 153249515 single base substitution T A exon_variant LICA-CN 4 153249515 153249515 single base substitution T A synonymous_variant T245T 735A>T LICA-CN 4 153249515 153249515 single base substitution T A synonymous_variant T303T 909A>T LICA-CN 4 153249515 153249515 single base substitution T A synonymous_variant T341T 1023A>T LICA-CN 4 153249515 153249515 single base substitution T A synonymous_variant T421T 1263A>T LICA-CN 4 153249515 153249515 single base substitution T A upstream_gene_variant LICA-CN 4 153303376 153303376 single base substitution T A intron_variant LICA-CN 4 153303376 153303376 single base substitution T A missense_variant I38F 112A>T LICA-CN 4 153332623 153332623 single base substitution C A missense_variant E111D 333G>T LICA-FR 4 153248249 153248249 single base substitution G C intron_variant LICA-FR 4 153248249 153248249 single base substitution G C upstream_gene_variant LICA-FR 4 153249506 153249506 single base substitution T C exon_variant LICA-FR 4 153249506 153249506 single base substitution T C synonymous_variant V248V 744A>G LICA-FR 4 153249506 153249506 single base substitution T C synonymous_variant V306V 918A>G LICA-FR 4 153249506 153249506 single base substitution T C synonymous_variant V344V 1032A>G LICA-FR 4 153249506 153249506 single base substitution T C synonymous_variant V424V 1272A>G LICA-FR 4 153249506 153249506 single base substitution T C upstream_gene_variant LICA-FR 4 153251904 153251904 single base substitution C G exon_variant LICA-FR 4 153251904 153251904 single base substitution C G missense_variant G192R 574G>C LICA-FR 4 153251904 153251904 single base substitution C G missense_variant G250R 748G>C LICA-FR 4 153251904 153251904 single base substitution C G missense_variant G288R 862G>C LICA-FR 4 153251904 153251904 single base substitution C G missense_variant G368R 1102G>C LICA-FR 4 153251904 153251904 single base substitution C G upstream_gene_variant LICA-FR 4 153265627 153265627 single base substitution A G downstream_gene_variant LICA-FR 4 153265627 153265627 single base substitution A G intron_variant LICA-FR 4 153267984 153267984 single base substitution C A exon_variant LICA-FR 4 153267984 153267984 single base substitution C A intron_variant LICA-FR 4 153305054 153305054 single base substitution T C intron_variant LICA-FR 4 153305054 153305054 single base substitution T C upstream_gene_variant LICA-FR 4 153321515 153321515 single base substitution C T intron_variant LICA-FR 4 153326062 153326062 single base substitution T C intron_variant LICA-FR 4 153327161 153327161 single base substitution C T intron_variant LICA-FR 4 153340647 153340647 insertion of <=200bp - AAACACAC intron_variant LICA-FR 4 153365289 153365289 single base substitution T A intron_variant LICA-FR 4 153381694 153381694 single base substitution T G intron_variant LICA-FR 4 153381715 153381715 single base substitution C T intron_variant LICA-FR 4 153386996 153386996 deletion of <=200bp A - intron_variant LICA-FR 4 153435095 153435095 single base substitution C T intron_variant LICA-FR 4 153449063 153449063 single base substitution C T downstream_gene_variant LICA-FR 4 153449063 153449063 single base substitution C T intron_variant LICA-FR 4 153454303 153454303 single base substitution T C intron_variant LIHC-US 4 153253841 153253841 single base substitution G T exon_variant LIHC-US 4 153253841 153253841 single base substitution G T missense_variant P122T 364C>A LIHC-US 4 153253841 153253841 single base substitution G T missense_variant P180T 538C>A LIHC-US 4 153253841 153253841 single base substitution G T missense_variant P218T 652C>A LIHC-US 4 153253841 153253841 single base substitution G T missense_variant P298T 892C>A LIHC-US 4 153253841 153253841 single base substitution G T upstream_gene_variant LIHC-US 4 153273838 153273838 single base substitution A T exon_variant LIHC-US 4 153273838 153273838 single base substitution A T intron_variant LIHC-US 4 153273838 153273838 single base substitution A T synonymous_variant L15L 45T>A LIHC-US 4 153273838 153273838 single base substitution A T upstream_gene_variant LINC-JP 4 153241922 153241922 single base substitution T C downstream_gene_variant LINC-JP 4 153249363 153249363 single base substitution T G exon_variant LINC-JP 4 153249363 153249363 single base substitution T G missense_variant K296T 887A>C LINC-JP 4 153249363 153249363 single base substitution T G missense_variant K354T 1061A>C LINC-JP 4 153249363 153249363 single base substitution T G missense_variant K392T 1175A>C LINC-JP 4 153249363 153249363 single base substitution T G missense_variant K472T 1415A>C LINC-JP 4 153249363 153249363 single base substitution T G upstream_gene_variant LINC-JP 4 153268050 153268050 single base substitution G C exon_variant LINC-JP 4 153268050 153268050 single base substitution G C intron_variant LINC-JP 4 153273593 153273594 deletion of <=200bp AT - intron_variant LINC-JP 4 153273593 153273594 deletion of <=200bp AT - upstream_gene_variant LINC-JP 4 153281786 153281786 single base substitution G T intron_variant LINC-JP 4 153285619 153285619 single base substitution T C intron_variant LINC-JP 4 153287000 153287000 single base substitution G A intron_variant LINC-JP 4 153298276 153298276 single base substitution A G intron_variant LINC-JP 4 153304886 153304886 single base substitution A T intron_variant LINC-JP 4 153304886 153304886 single base substitution A T upstream_gene_variant LINC-JP 4 153331033 153331033 single base substitution T C downstream_gene_variant LINC-JP 4 153331033 153331033 single base substitution T C intron_variant LINC-JP 4 153345101 153345101 single base substitution T A intron_variant LINC-JP 4 153360143 153360143 single base substitution T C intron_variant LINC-JP 4 153373796 153373796 single base substitution C T intron_variant LINC-JP 4 153375205 153375205 single base substitution C A intron_variant LINC-JP 4 153377952 153377952 single base substitution G T intron_variant LINC-JP 4 153384865 153384865 single base substitution T C intron_variant LINC-JP 4 153388610 153388610 single base substitution A G intron_variant LINC-JP 4 153394452 153394452 single base substitution T C intron_variant LINC-JP 4 153401893 153401893 single base substitution A C intron_variant LINC-JP 4 153429819 153429819 single base substitution G A intron_variant LINC-JP 4 153440475 153440475 single base substitution G T intron_variant LINC-JP 4 153445691 153445691 single base substitution T C intron_variant LIRI-JP 4 153238029 153238029 single base substitution C T downstream_gene_variant LIRI-JP 4 153238295 153238295 single base substitution T A downstream_gene_variant LIRI-JP 4 153239143 153239143 single base substitution T C downstream_gene_variant LIRI-JP 4 153239479 153239479 single base substitution T A downstream_gene_variant LIRI-JP 4 153240231 153240231 single base substitution C T downstream_gene_variant LIRI-JP 4 153242192 153242192 single base substitution C A downstream_gene_variant LIRI-JP 4 153243649 153243649 single base substitution G A 3_prime_UTR_variant LIRI-JP 4 153243649 153243649 single base substitution G A downstream_gene_variant LIRI-JP 4 153244959 153244959 single base substitution T C downstream_gene_variant LIRI-JP 4 153244959 153244959 single base substitution T C exon_variant LIRI-JP 4 153244959 153244959 single base substitution T C intron_variant LIRI-JP 4 153245363 153245363 deletion of <=200bp T - downstream_gene_variant LIRI-JP 4 153245363 153245363 deletion of <=200bp T - exon_variant LIRI-JP 4 153245363 153245363 deletion of <=200bp T - frameshift_variant T434 LIRI-JP 4 153245363 153245363 deletion of <=200bp T - frameshift_variant T492 LIRI-JP 4 153245363 153245363 deletion of <=200bp T - frameshift_variant T530 LIRI-JP 4 153245363 153245363 deletion of <=200bp T - frameshift_variant T610 LIRI-JP 4 153247364 153247364 single base substitution C T downstream_gene_variant LIRI-JP 4 153247364 153247364 single base substitution C T exon_variant LIRI-JP 4 153247364 153247364 single base substitution C T missense_variant D304N 910G>A LIRI-JP 4 153247364 153247364 single base substitution C T missense_variant D362N 1084G>A LIRI-JP 4 153247364 153247364 single base substitution C T missense_variant D400N 1198G>A LIRI-JP 4 153247364 153247364 single base substitution C T missense_variant D480N 1438G>A LIRI-JP 4 153247364 153247364 single base substitution C T upstream_gene_variant LIRI-JP 4 153252142 153252142 single base substitution G A intron_variant LIRI-JP 4 153252142 153252142 single base substitution G A upstream_gene_variant LIRI-JP 4 153252286 153252286 single base substitution T C intron_variant LIRI-JP 4 153252286 153252286 single base substitution T C upstream_gene_variant LIRI-JP 4 153253272 153253272 single base substitution G A intron_variant LIRI-JP 4 153253272 153253272 single base substitution G A upstream_gene_variant LIRI-JP 4 153253731 153253731 single base substitution G A intron_variant LIRI-JP 4 153253731 153253731 single base substitution G A upstream_gene_variant LIRI-JP 4 153254803 153254803 single base substitution G A intron_variant LIRI-JP 4 153254803 153254803 single base substitution G A upstream_gene_variant LIRI-JP 4 153255322 153255322 single base substitution A C intron_variant LIRI-JP 4 153255322 153255322 single base substitution A C upstream_gene_variant LIRI-JP 4 153256538 153256538 single base substitution T G intron_variant LIRI-JP 4 153256538 153256538 single base substitution T G upstream_gene_variant LIRI-JP 4 153257565 153257565 single base substitution T A intron_variant LIRI-JP 4 153257565 153257565 single base substitution T A upstream_gene_variant LIRI-JP 4 153257958 153257958 single base substitution C T intron_variant LIRI-JP 4 153257958 153257958 single base substitution C T upstream_gene_variant LIRI-JP 4 153258424 153258424 single base substitution T C intron_variant LIRI-JP 4 153258424 153258424 single base substitution T C upstream_gene_variant LIRI-JP 4 153259115 153259115 single base substitution T C intron_variant LIRI-JP 4 153259452 153259452 single base substitution T C intron_variant LIRI-JP 4 153264675 153264675 single base substitution G A downstream_gene_variant LIRI-JP 4 153264675 153264675 single base substitution G A intron_variant LIRI-JP 4 153264806 153264806 single base substitution T A downstream_gene_variant LIRI-JP 4 153264806 153264806 single base substitution T A intron_variant LIRI-JP 4 153265864 153265864 single base substitution A G downstream_gene_variant LIRI-JP 4 153265864 153265864 single base substitution A G intron_variant LIRI-JP 4 153265885 153265885 single base substitution A G downstream_gene_variant LIRI-JP 4 153265885 153265885 single base substitution A G intron_variant LIRI-JP 4 153266666 153266666 single base substitution T C downstream_gene_variant LIRI-JP 4 153266666 153266666 single base substitution T C intron_variant LIRI-JP 4 153267363 153267363 single base substitution T C downstream_gene_variant LIRI-JP 4 153267363 153267363 single base substitution T C intron_variant LIRI-JP 4 153268814 153268814 single base substitution C A intron_variant LIRI-JP 4 153268983 153268983 single base substitution T C intron_variant LIRI-JP 4 153270811 153270811 single base substitution T C intron_variant LIRI-JP 4 153270811 153270811 single base substitution T C upstream_gene_variant LIRI-JP 4 153271363 153271363 single base substitution T G intron_variant LIRI-JP 4 153271363 153271363 single base substitution T G upstream_gene_variant LIRI-JP 4 153275879 153275879 single base substitution T G intron_variant LIRI-JP 4 153275879 153275879 single base substitution T G upstream_gene_variant LIRI-JP 4 153275887 153275887 single base substitution T A intron_variant LIRI-JP 4 153275887 153275887 single base substitution T A upstream_gene_variant LIRI-JP 4 153276015 153276015 single base substitution G T intron_variant LIRI-JP 4 153276015 153276015 single base substitution G T upstream_gene_variant LIRI-JP 4 153276077 153276077 single base substitution T C intron_variant LIRI-JP 4 153276077 153276077 single base substitution T C upstream_gene_variant LIRI-JP 4 153276977 153276977 single base substitution T C intron_variant LIRI-JP 4 153276977 153276977 single base substitution T C upstream_gene_variant LIRI-JP 4 153277415 153277415 single base substitution T C intron_variant LIRI-JP 4 153277415 153277415 single base substitution T C upstream_gene_variant LIRI-JP 4 153277659 153277659 single base substitution C A intron_variant LIRI-JP 4 153277659 153277659 single base substitution C A upstream_gene_variant LIRI-JP 4 153280914 153280914 single base substitution T C intron_variant LIRI-JP 4 153282249 153282249 single base substitution T G intron_variant LIRI-JP 4 153282496 153282496 insertion of <=200bp - AT intron_variant LIRI-JP 4 153282595 153282595 single base substitution T C intron_variant LIRI-JP 4 153284019 153284019 single base substitution A G intron_variant LIRI-JP 4 153284588 153284588 single base substitution C T intron_variant LIRI-JP 4 153286673 153286673 single base substitution T C intron_variant LIRI-JP 4 153287321 153287321 single base substitution T C intron_variant LIRI-JP 4 153287597 153287597 single base substitution G T intron_variant LIRI-JP 4 153290554 153290554 single base substitution G A intron_variant LIRI-JP 4 153291146 153291146 single base substitution T C intron_variant LIRI-JP 4 153291942 153291942 single base substitution T C intron_variant LIRI-JP 4 153292236 153292236 single base substitution C T intron_variant LIRI-JP 4 153293579 153293579 single base substitution T C intron_variant LIRI-JP 4 153294878 153294878 single base substitution C T intron_variant LIRI-JP 4 153295865 153295865 single base substitution T C intron_variant LIRI-JP 4 153299170 153299170 single base substitution T C intron_variant LIRI-JP 4 153299469 153299469 single base substitution T C intron_variant LIRI-JP 4 153302516 153302516 single base substitution G T intron_variant LIRI-JP 4 153302606 153302606 single base substitution G A intron_variant LIRI-JP 4 153304200 153304200 single base substitution T C intron_variant LIRI-JP 4 153304200 153304200 single base substitution T C upstream_gene_variant LIRI-JP 4 153307065 153307065 single base substitution T C intron_variant LIRI-JP 4 153307065 153307065 single base substitution T C upstream_gene_variant LIRI-JP 4 153308029 153308029 single base substitution C A intron_variant LIRI-JP 4 153308029 153308029 single base substitution C A upstream_gene_variant LIRI-JP 4 153309365 153309365 single base substitution T C intron_variant LIRI-JP 4 153309611 153309611 single base substitution A C intron_variant LIRI-JP 4 153312630 153312630 single base substitution C A intron_variant LIRI-JP 4 153313702 153313702 single base substitution C G intron_variant LIRI-JP 4 153319798 153319798 single base substitution C G intron_variant LIRI-JP 4 153325210 153325210 single base substitution G C intron_variant LIRI-JP 4 153329578 153329578 single base substitution T A downstream_gene_variant LIRI-JP 4 153329578 153329578 single base substitution T A intron_variant LIRI-JP 4 153330157 153330157 single base substitution G A downstream_gene_variant LIRI-JP 4 153330157 153330157 single base substitution G A intron_variant LIRI-JP 4 153330693 153330693 single base substitution G A downstream_gene_variant LIRI-JP 4 153330693 153330693 single base substitution G A intron_variant LIRI-JP 4 153330771 153330771 single base substitution T A downstream_gene_variant LIRI-JP 4 153330771 153330771 single base substitution T A intron_variant LIRI-JP 4 153333988 153333988 single base substitution A T intron_variant LIRI-JP 4 153333988 153333988 single base substitution A T upstream_gene_variant LIRI-JP 4 153334020 153334020 single base substitution T C intron_variant LIRI-JP 4 153334020 153334020 single base substitution T C upstream_gene_variant LIRI-JP 4 153334050 153334050 single base substitution T C intron_variant LIRI-JP 4 153334050 153334050 single base substitution T C upstream_gene_variant LIRI-JP 4 153337199 153337199 single base substitution T C intron_variant LIRI-JP 4 153337199 153337199 single base substitution T C upstream_gene_variant LIRI-JP 4 153338008 153338008 single base substitution A C intron_variant LIRI-JP 4 153338008 153338008 single base substitution A C upstream_gene_variant LIRI-JP 4 153338144 153338144 single base substitution T C intron_variant LIRI-JP 4 153338144 153338144 single base substitution T C upstream_gene_variant LIRI-JP 4 153339365 153339365 single base substitution T C intron_variant LIRI-JP 4 153340801 153340801 single base substitution A C intron_variant LIRI-JP 4 153344355 153344355 single base substitution C A intron_variant LIRI-JP 4 153346865 153346865 single base substitution C G intron_variant LIRI-JP 4 153349222 153349222 single base substitution T G intron_variant LIRI-JP 4 153349524 153349540 deletion of <=200bp TTTTATACTTACAAAAT - intron_variant LIRI-JP 4 153349867 153349867 deletion of <=200bp G - intron_variant LIRI-JP 4 153351151 153351151 single base substitution G A intron_variant LIRI-JP 4 153352123 153352123 single base substitution A G intron_variant LIRI-JP 4 153353357 153353357 single base substitution T C intron_variant LIRI-JP 4 153353641 153353641 single base substitution T C intron_variant LIRI-JP 4 153357366 153357366 single base substitution T A intron_variant LIRI-JP 4 153360171 153360171 single base substitution T C intron_variant LIRI-JP 4 153362223 153362223 single base substitution T C intron_variant LIRI-JP 4 153364124 153364124 single base substitution A G intron_variant LIRI-JP 4 153364172 153364172 single base substitution T C intron_variant LIRI-JP 4 153368195 153368195 single base substitution T C intron_variant LIRI-JP 4 153368553 153368553 single base substitution G C intron_variant LIRI-JP 4 153370235 153370235 single base substitution T C intron_variant LIRI-JP 4 153370771 153370771 single base substitution T C intron_variant LIRI-JP 4 153372100 153372100 single base substitution T C intron_variant LIRI-JP 4 153373358 153373358 single base substitution C T intron_variant LIRI-JP 4 153373805 153373805 single base substitution G A intron_variant LIRI-JP 4 153376618 153376618 single base substitution T C intron_variant LIRI-JP 4 153377086 153377086 single base substitution T C intron_variant LIRI-JP 4 153378249 153378249 single base substitution T C intron_variant LIRI-JP 4 153378986 153378986 single base substitution C T intron_variant LIRI-JP 4 153380044 153380044 single base substitution T C intron_variant LIRI-JP 4 153382337 153382337 single base substitution G A intron_variant LIRI-JP 4 153386330 153386330 single base substitution G T intron_variant LIRI-JP 4 153386848 153386848 single base substitution T C intron_variant LIRI-JP 4 153389066 153389066 single base substitution T A intron_variant LIRI-JP 4 153389109 153389109 single base substitution T C intron_variant LIRI-JP 4 153389257 153389257 single base substitution C T intron_variant LIRI-JP 4 153390537 153390537 single base substitution A G intron_variant LIRI-JP 4 153390813 153390813 single base substitution A C intron_variant LIRI-JP 4 153392156 153392156 single base substitution C T intron_variant LIRI-JP 4 153392399 153392400 deletion of <=200bp TA - intron_variant LIRI-JP 4 153392800 153392800 single base substitution C G intron_variant LIRI-JP 4 153393065 153393065 single base substitution T C intron_variant LIRI-JP 4 153394242 153394242 single base substitution T C intron_variant LIRI-JP 4 153395527 153395527 single base substitution T C intron_variant LIRI-JP 4 153395533 153395533 single base substitution G T intron_variant LIRI-JP 4 153400817 153400817 single base substitution A T intron_variant LIRI-JP 4 153400966 153400966 single base substitution T A intron_variant LIRI-JP 4 153401351 153401351 single base substitution C T intron_variant LIRI-JP 4 153401576 153401576 single base substitution A G intron_variant LIRI-JP 4 153403068 153403068 single base substitution T C intron_variant LIRI-JP 4 153403487 153403487 single base substitution T C intron_variant LIRI-JP 4 153403544 153403544 single base substitution T C intron_variant LIRI-JP 4 153404463 153404463 single base substitution T C intron_variant LIRI-JP 4 153407043 153407043 single base substitution G T intron_variant LIRI-JP 4 153411557 153411557 single base substitution C T intron_variant LIRI-JP 4 153412316 153412316 single base substitution A G intron_variant LIRI-JP 4 153412601 153412601 single base substitution A G intron_variant LIRI-JP 4 153412616 153412616 single base substitution A T intron_variant LIRI-JP 4 153418604 153418604 single base substitution A G intron_variant LIRI-JP 4 153418687 153418687 single base substitution G T intron_variant LIRI-JP 4 153419161 153419161 insertion of <=200bp - T intron_variant LIRI-JP 4 153419296 153419296 insertion of <=200bp - T intron_variant LIRI-JP 4 153421856 153421856 single base substitution T C intron_variant LIRI-JP 4 153422198 153422198 single base substitution A T intron_variant LIRI-JP 4 153427865 153427865 single base substitution T C intron_variant LIRI-JP 4 153432267 153432267 single base substitution C A intron_variant LIRI-JP 4 153433359 153433359 single base substitution T C intron_variant LIRI-JP 4 153433853 153433853 single base substitution T C intron_variant LIRI-JP 4 153434694 153434694 single base substitution A T intron_variant LIRI-JP 4 153438120 153438120 single base substitution G A intron_variant LIRI-JP 4 153440158 153440158 single base substitution T A intron_variant LIRI-JP 4 153442213 153442213 single base substitution C T intron_variant LIRI-JP 4 153443959 153443959 single base substitution C G intron_variant LIRI-JP 4 153448571 153448571 single base substitution T C downstream_gene_variant LIRI-JP 4 153448571 153448571 single base substitution T C intron_variant LIRI-JP 4 153449057 153449057 single base substitution T C downstream_gene_variant LIRI-JP 4 153449057 153449057 single base substitution T C intron_variant LIRI-JP 4 153449063 153449063 single base substitution C T downstream_gene_variant LIRI-JP 4 153449063 153449063 single base substitution C T intron_variant LIRI-JP 4 153449855 153449855 single base substitution T C downstream_gene_variant LIRI-JP 4 153449855 153449855 single base substitution T C intron_variant LIRI-JP 4 153450240 153450240 single base substitution C G downstream_gene_variant LIRI-JP 4 153450240 153450240 single base substitution C G intron_variant LIRI-JP 4 153452637 153452637 single base substitution G A intron_variant LIRI-JP 4 153453890 153453891 deletion of <=200bp GT - intron_variant LIRI-JP 4 153455614 153455614 single base substitution T A intron_variant LIRI-JP 4 153455940 153455940 single base substitution C A intron_variant LIRI-JP 4 153460588 153460588 single base substitution A G upstream_gene_variant LUSC-KR 4 153241624 153241624 single base substitution T C downstream_gene_variant LUSC-KR 4 153258986 153258986 single base substitution G A stop_gained Q101* 301C>T LUSC-KR 4 153258986 153258986 single base substitution G A stop_gained Q159* 475C>T LUSC-KR 4 153258986 153258986 single base substitution G A stop_gained Q197* 589C>T LUSC-KR 4 153258986 153258986 single base substitution G A stop_gained Q277* 829C>T LUSC-KR 4 153266761 153266761 single base substitution G A downstream_gene_variant LUSC-KR 4 153266761 153266761 single base substitution G A intron_variant LUSC-KR 4 153279611 153279611 single base substitution C T intron_variant LUSC-KR 4 153285365 153285365 single base substitution G A intron_variant LUSC-KR 4 153285366 153285366 single base substitution G T intron_variant LUSC-KR 4 153295392 153295392 single base substitution C T intron_variant LUSC-KR 4 153297806 153297806 single base substitution C T intron_variant LUSC-KR 4 153304043 153304043 single base substitution C A intron_variant LUSC-KR 4 153304043 153304043 single base substitution C A upstream_gene_variant LUSC-KR 4 153315194 153315194 single base substitution C T intron_variant LUSC-KR 4 153317948 153317948 single base substitution G C intron_variant LUSC-KR 4 153322599 153322599 single base substitution C T intron_variant LUSC-KR 4 153322764 153322764 single base substitution C A intron_variant LUSC-KR 4 153350048 153350048 single base substitution C A intron_variant LUSC-KR 4 153355619 153355619 single base substitution T C intron_variant LUSC-KR 4 153365659 153365659 single base substitution T G intron_variant LUSC-KR 4 153372026 153372026 single base substitution T C intron_variant LUSC-KR 4 153375415 153375415 single base substitution T C intron_variant LUSC-KR 4 153384119 153384119 single base substitution G T intron_variant LUSC-KR 4 153396744 153396744 single base substitution G A intron_variant LUSC-KR 4 153406247 153406247 single base substitution C A intron_variant LUSC-KR 4 153406248 153406248 single base substitution C A intron_variant LUSC-KR 4 153418694 153418694 single base substitution C T intron_variant LUSC-KR 4 153423342 153423342 single base substitution C G intron_variant LUSC-KR 4 153440089 153440089 single base substitution A G intron_variant LUSC-KR 4 153441461 153441461 single base substitution T C intron_variant LUSC-KR 4 153441554 153441554 single base substitution C A intron_variant LUSC-KR 4 153449075 153449075 single base substitution C T downstream_gene_variant LUSC-KR 4 153449075 153449075 single base substitution C T intron_variant LUSC-US 4 153244124 153244124 single base substitution G C downstream_gene_variant LUSC-US 4 153244124 153244124 single base substitution G C exon_variant LUSC-US 4 153244124 153244124 single base substitution G C stop_gained S502* 1505C>G LUSC-US 4 153244124 153244124 single base substitution G C stop_gained S560* 1679C>G LUSC-US 4 153244124 153244124 single base substitution G C stop_gained S598* 1793C>G LUSC-US 4 153244124 153244124 single base substitution G C stop_gained S678* 2033C>G LUSC-US 4 153244155 153244155 insertion of <=200bp - C downstream_gene_variant LUSC-US 4 153244155 153244155 insertion of <=200bp - C exon_variant LUSC-US 4 153244155 153244155 insertion of <=200bp - C frameshift_variant S492R? LUSC-US 4 153244155 153244155 insertion of <=200bp - C frameshift_variant S550R? LUSC-US 4 153244155 153244155 insertion of <=200bp - C frameshift_variant S588R? LUSC-US 4 153244155 153244155 insertion of <=200bp - C frameshift_variant S668R? LUSC-US 4 153244194 153244194 single base substitution C A downstream_gene_variant LUSC-US 4 153244194 153244194 single base substitution C A exon_variant LUSC-US 4 153244194 153244194 single base substitution C A stop_gained E479* 1435G>T LUSC-US 4 153244194 153244194 single base substitution C A stop_gained E537* 1609G>T LUSC-US 4 153244194 153244194 single base substitution C A stop_gained E575* 1723G>T LUSC-US 4 153244194 153244194 single base substitution C A stop_gained E655* 1963G>T LUSC-US 4 153244198 153244198 single base substitution C G downstream_gene_variant LUSC-US 4 153244198 153244198 single base substitution C G exon_variant LUSC-US 4 153244198 153244198 single base substitution C G synonymous_variant T477T 1431G>C LUSC-US 4 153244198 153244198 single base substitution C G synonymous_variant T535T 1605G>C LUSC-US 4 153244198 153244198 single base substitution C G synonymous_variant T573T 1719G>C LUSC-US 4 153244198 153244198 single base substitution C G synonymous_variant T653T 1959G>C LUSC-US 4 153245437 153245437 single base substitution C G downstream_gene_variant LUSC-US 4 153245437 153245437 single base substitution C G exon_variant LUSC-US 4 153245437 153245437 single base substitution C G missense_variant S409T 1226G>C LUSC-US 4 153245437 153245437 single base substitution C G missense_variant S467T 1400G>C LUSC-US 4 153245437 153245437 single base substitution C G missense_variant S505T 1514G>C LUSC-US 4 153245437 153245437 single base substitution C G missense_variant S585T 1754G>C LUSC-US 4 153247252 153247252 single base substitution C T downstream_gene_variant LUSC-US 4 153247252 153247252 single base substitution C T exon_variant LUSC-US 4 153247252 153247252 single base substitution C T missense_variant G341E 1022G>A LUSC-US 4 153247252 153247252 single base substitution C T missense_variant G399E 1196G>A LUSC-US 4 153247252 153247252 single base substitution C T missense_variant G437E 1310G>A LUSC-US 4 153247252 153247252 single base substitution C T missense_variant G517E 1550G>A LUSC-US 4 153247252 153247252 single base substitution C T upstream_gene_variant LUSC-US 4 153247289 153247289 single base substitution G C downstream_gene_variant LUSC-US 4 153247289 153247289 single base substitution G C exon_variant LUSC-US 4 153247289 153247289 single base substitution G C missense_variant R329G 985C>G LUSC-US 4 153247289 153247289 single base substitution G C missense_variant R387G 1159C>G LUSC-US 4 153247289 153247289 single base substitution G C missense_variant R425G 1273C>G LUSC-US 4 153247289 153247289 single base substitution G C missense_variant R505G 1513C>G LUSC-US 4 153247289 153247289 single base substitution G C upstream_gene_variant LUSC-US 4 153247289 153247289 single base substitution G T downstream_gene_variant LUSC-US 4 153247289 153247289 single base substitution G T exon_variant LUSC-US 4 153247289 153247289 single base substitution G T missense_variant R329S 985C>A LUSC-US 4 153247289 153247289 single base substitution G T missense_variant R387S 1159C>A LUSC-US 4 153247289 153247289 single base substitution G T missense_variant R425S 1273C>A LUSC-US 4 153247289 153247289 single base substitution G T missense_variant R505S 1513C>A LUSC-US 4 153247289 153247289 single base substitution G T upstream_gene_variant LUSC-US 4 153247367 153247367 single base substitution G A downstream_gene_variant LUSC-US 4 153247367 153247367 single base substitution G A exon_variant LUSC-US 4 153247367 153247367 single base substitution G A stop_gained R303* 907C>T LUSC-US 4 153247367 153247367 single base substitution G A stop_gained R361* 1081C>T LUSC-US 4 153247367 153247367 single base substitution G A stop_gained R399* 1195C>T LUSC-US 4 153247367 153247367 single base substitution G A stop_gained R479* 1435C>T LUSC-US 4 153247367 153247367 single base substitution G A upstream_gene_variant LUSC-US 4 153247367 153247367 single base substitution G T downstream_gene_variant LUSC-US 4 153247367 153247367 single base substitution G T exon_variant LUSC-US 4 153247367 153247367 single base substitution G T synonymous_variant R303R 907C>A LUSC-US 4 153247367 153247367 single base substitution G T synonymous_variant R361R 1081C>A LUSC-US 4 153247367 153247367 single base substitution G T synonymous_variant R399R 1195C>A LUSC-US 4 153247367 153247367 single base substitution G T synonymous_variant R479R 1435C>A LUSC-US 4 153247367 153247367 single base substitution G T upstream_gene_variant LUSC-US 4 153249384 153249384 single base substitution C T exon_variant LUSC-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A LUSC-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A LUSC-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A LUSC-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A LUSC-US 4 153249384 153249384 single base substitution C T upstream_gene_variant LUSC-US 4 153249410 153249410 single base substitution G T exon_variant LUSC-US 4 153249410 153249410 single base substitution G T synonymous_variant T280T 840C>A LUSC-US 4 153249410 153249410 single base substitution G T synonymous_variant T338T 1014C>A LUSC-US 4 153249410 153249410 single base substitution G T synonymous_variant T376T 1128C>A LUSC-US 4 153249410 153249410 single base substitution G T synonymous_variant T456T 1368C>A LUSC-US 4 153249410 153249410 single base substitution G T upstream_gene_variant LUSC-US 4 153271243 153271243 single base substitution G A exon_variant LUSC-US 4 153271243 153271243 single base substitution G A missense_variant R179C 535C>T LUSC-US 4 153271243 153271243 single base substitution G A missense_variant R61C 181C>T LUSC-US 4 153271243 153271243 single base substitution G A missense_variant R99C 295C>T LUSC-US 4 153271243 153271243 single base substitution G A upstream_gene_variant MALY-DE 4 153240893 153240893 single base substitution C T downstream_gene_variant MALY-DE 4 153242204 153242204 single base substitution C G downstream_gene_variant MALY-DE 4 153242921 153242921 single base substitution C G 3_prime_UTR_variant MALY-DE 4 153242921 153242921 single base substitution C G downstream_gene_variant MALY-DE 4 153243137 153243137 single base substitution C G 3_prime_UTR_variant MALY-DE 4 153243137 153243137 single base substitution C G downstream_gene_variant MALY-DE 4 153243340 153243340 single base substitution C G 3_prime_UTR_variant MALY-DE 4 153243340 153243340 single base substitution C G downstream_gene_variant MALY-DE 4 153243385 153243385 single base substitution C G 3_prime_UTR_variant MALY-DE 4 153243385 153243385 single base substitution C G downstream_gene_variant MALY-DE 4 153243905 153243905 single base substitution C G 3_prime_UTR_variant MALY-DE 4 153243905 153243905 single base substitution C G downstream_gene_variant MALY-DE 4 153244836 153244836 single base substitution C T downstream_gene_variant MALY-DE 4 153244836 153244836 single base substitution C T exon_variant MALY-DE 4 153244836 153244836 single base substitution C T intron_variant MALY-DE 4 153245297 153245297 single base substitution C T downstream_gene_variant MALY-DE 4 153245297 153245297 single base substitution C T exon_variant MALY-DE 4 153245297 153245297 single base substitution C T intron_variant MALY-DE 4 153245911 153245911 single base substitution C T downstream_gene_variant MALY-DE 4 153245911 153245911 single base substitution C T exon_variant MALY-DE 4 153245911 153245911 single base substitution C T intron_variant MALY-DE 4 153245911 153245911 single base substitution C T upstream_gene_variant MALY-DE 4 153249007 153249007 single base substitution T C intron_variant MALY-DE 4 153249007 153249007 single base substitution T C upstream_gene_variant MALY-DE 4 153252619 153252619 single base substitution A C intron_variant MALY-DE 4 153252619 153252619 single base substitution A C upstream_gene_variant MALY-DE 4 153255205 153255205 insertion of <=200bp - CAA intron_variant MALY-DE 4 153255205 153255205 insertion of <=200bp - CAA upstream_gene_variant MALY-DE 4 153257193 153257193 single base substitution T G intron_variant MALY-DE 4 153257193 153257193 single base substitution T G upstream_gene_variant MALY-DE 4 153273302 153273302 deletion of <=200bp C - intron_variant MALY-DE 4 153273302 153273302 deletion of <=200bp C - upstream_gene_variant MALY-DE 4 153278344 153278344 single base substitution T G intron_variant MALY-DE 4 153278344 153278344 single base substitution T G upstream_gene_variant MALY-DE 4 153285552 153285552 single base substitution A G intron_variant MALY-DE 4 153295823 153295823 single base substitution A T intron_variant MALY-DE 4 153297645 153297645 single base substitution T G intron_variant MALY-DE 4 153311172 153311172 single base substitution A T intron_variant MALY-DE 4 153313633 153313633 single base substitution A T intron_variant MALY-DE 4 153321670 153321670 single base substitution T C intron_variant MALY-DE 4 153322436 153322436 single base substitution G A intron_variant MALY-DE 4 153323149 153323149 single base substitution T A intron_variant MALY-DE 4 153330542 153330542 single base substitution G A downstream_gene_variant MALY-DE 4 153330542 153330542 single base substitution G A intron_variant MALY-DE 4 153332047 153332047 single base substitution T A downstream_gene_variant MALY-DE 4 153332047 153332047 single base substitution T A intron_variant MALY-DE 4 153332080 153332080 single base substitution G C downstream_gene_variant MALY-DE 4 153332080 153332080 single base substitution G C intron_variant MALY-DE 4 153333359 153333359 single base substitution C G intron_variant MALY-DE 4 153333359 153333359 single base substitution C G upstream_gene_variant MALY-DE 4 153333844 153333844 single base substitution A G intron_variant MALY-DE 4 153333844 153333844 single base substitution A G upstream_gene_variant MALY-DE 4 153335079 153335079 single base substitution C A intron_variant MALY-DE 4 153335079 153335079 single base substitution C A upstream_gene_variant MALY-DE 4 153351119 153351119 insertion of <=200bp - TTG intron_variant MALY-DE 4 153352110 153352110 single base substitution T A intron_variant MALY-DE 4 153352147 153352147 single base substitution T A intron_variant MALY-DE 4 153352691 153352691 single base substitution G A intron_variant MALY-DE 4 153362276 153362276 single base substitution G A intron_variant MALY-DE 4 153372517 153372517 single base substitution A T intron_variant MALY-DE 4 153373469 153373469 single base substitution T A intron_variant MALY-DE 4 153375039 153375039 single base substitution A C intron_variant MALY-DE 4 153375715 153375715 insertion of <=200bp - A intron_variant MALY-DE 4 153375943 153375943 single base substitution G A intron_variant MALY-DE 4 153382635 153382635 single base substitution C T intron_variant MALY-DE 4 153396423 153396423 single base substitution A T intron_variant MALY-DE 4 153409460 153409460 single base substitution T C intron_variant MALY-DE 4 153409596 153409596 single base substitution G A intron_variant MALY-DE 4 153412112 153412112 single base substitution T C intron_variant MALY-DE 4 153413473 153413473 single base substitution G A intron_variant MALY-DE 4 153418185 153418185 single base substitution G A intron_variant MALY-DE 4 153420010 153420010 single base substitution G A intron_variant MALY-DE 4 153429004 153429004 single base substitution G A intron_variant MALY-DE 4 153440475 153440475 single base substitution G T intron_variant MALY-DE 4 153449949 153449949 single base substitution A C downstream_gene_variant MALY-DE 4 153449949 153449949 single base substitution A C intron_variant MALY-DE 4 153454569 153454569 single base substitution G A intron_variant MALY-DE 4 153459504 153459504 single base substitution A C upstream_gene_variant MALY-DE 4 153460239 153460239 single base substitution G C upstream_gene_variant MALY-DE 4 153460546 153460546 single base substitution T C upstream_gene_variant MELA-AU 4 153237578 153237578 single base substitution G A downstream_gene_variant MELA-AU 4 153237855 153237855 single base substitution G A downstream_gene_variant MELA-AU 4 153238032 153238032 single base substitution G A downstream_gene_variant MELA-AU 4 153238871 153238871 single base substitution T C downstream_gene_variant MELA-AU 4 153238968 153238968 single base substitution A G downstream_gene_variant MELA-AU 4 153240096 153240096 single base substitution G A downstream_gene_variant MELA-AU 4 153240103 153240103 single base substitution T G downstream_gene_variant MELA-AU 4 153241246 153241246 single base substitution G A downstream_gene_variant MELA-AU 4 153241484 153241484 single base substitution G A downstream_gene_variant MELA-AU 4 153241641 153241641 single base substitution A G downstream_gene_variant MELA-AU 4 153242378 153242378 single base substitution G A downstream_gene_variant MELA-AU 4 153243978 153243978 single base substitution G A 3_prime_UTR_variant MELA-AU 4 153243978 153243978 single base substitution G A downstream_gene_variant MELA-AU 4 153243978 153243978 single base substitution G A exon_variant MELA-AU 4 153244135 153244135 single base substitution C T downstream_gene_variant MELA-AU 4 153244135 153244135 single base substitution C T exon_variant MELA-AU 4 153244135 153244135 single base substitution C T synonymous_variant R498R 1494G>A MELA-AU 4 153244135 153244135 single base substitution C T synonymous_variant R556R 1668G>A MELA-AU 4 153244135 153244135 single base substitution C T synonymous_variant R594R 1782G>A MELA-AU 4 153244135 153244135 single base substitution C T synonymous_variant R674R 2022G>A MELA-AU 4 153245292 153245292 single base substitution G A downstream_gene_variant MELA-AU 4 153245292 153245292 single base substitution G A exon_variant MELA-AU 4 153245292 153245292 single base substitution G A intron_variant MELA-AU 4 153245446 153245446 single base substitution G A downstream_gene_variant MELA-AU 4 153245446 153245446 single base substitution G A exon_variant MELA-AU 4 153245446 153245446 single base substitution G A missense_variant S406L 1217C>T MELA-AU 4 153245446 153245446 single base substitution G A missense_variant S464L 1391C>T MELA-AU 4 153245446 153245446 single base substitution G A missense_variant S502L 1505C>T MELA-AU 4 153245446 153245446 single base substitution G A missense_variant S582L 1745C>T MELA-AU 4 153245448 153245448 single base substitution C T downstream_gene_variant MELA-AU 4 153245448 153245448 single base substitution C T exon_variant MELA-AU 4 153245448 153245448 single base substitution C T synonymous_variant Q405Q 1215G>A MELA-AU 4 153245448 153245448 single base substitution C T synonymous_variant Q463Q 1389G>A MELA-AU 4 153245448 153245448 single base substitution C T synonymous_variant Q501Q 1503G>A MELA-AU 4 153245448 153245448 single base substitution C T synonymous_variant Q581Q 1743G>A MELA-AU 4 153245518 153245518 single base substitution G A downstream_gene_variant MELA-AU 4 153245518 153245518 single base substitution G A exon_variant MELA-AU 4 153245518 153245518 single base substitution G A missense_variant S382F 1145C>T MELA-AU 4 153245518 153245518 single base substitution G A missense_variant S440F 1319C>T MELA-AU 4 153245518 153245518 single base substitution G A missense_variant S478F 1433C>T MELA-AU 4 153245518 153245518 single base substitution G A missense_variant S558F 1673C>T MELA-AU 4 153246045 153246045 single base substitution A G downstream_gene_variant MELA-AU 4 153246045 153246045 single base substitution A G exon_variant MELA-AU 4 153246045 153246045 single base substitution A G intron_variant MELA-AU 4 153246045 153246045 single base substitution A G upstream_gene_variant MELA-AU 4 153246218 153246219 multiple base substitution (>=2bp and <=200bp) GT AA downstream_gene_variant MELA-AU 4 153246218 153246219 multiple base substitution (>=2bp and <=200bp) GT AA exon_variant MELA-AU 4 153246218 153246219 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 4 153246218 153246219 multiple base substitution (>=2bp and <=200bp) GT AA upstream_gene_variant MELA-AU 4 153246508 153246508 single base substitution G A downstream_gene_variant MELA-AU 4 153246508 153246508 single base substitution G A exon_variant MELA-AU 4 153246508 153246508 single base substitution G A intron_variant MELA-AU 4 153246508 153246508 single base substitution G A upstream_gene_variant MELA-AU 4 153246823 153246823 single base substitution T A downstream_gene_variant MELA-AU 4 153246823 153246823 single base substitution T A exon_variant MELA-AU 4 153246823 153246823 single base substitution T A intron_variant MELA-AU 4 153246823 153246823 single base substitution T A upstream_gene_variant MELA-AU 4 153247373 153247373 single base substitution C T downstream_gene_variant MELA-AU 4 153247373 153247373 single base substitution C T exon_variant MELA-AU 4 153247373 153247373 single base substitution C T missense_variant G301S 901G>A MELA-AU 4 153247373 153247373 single base substitution C T missense_variant G359S 1075G>A MELA-AU 4 153247373 153247373 single base substitution C T missense_variant G397S 1189G>A MELA-AU 4 153247373 153247373 single base substitution C T missense_variant G477S 1429G>A MELA-AU 4 153247373 153247373 single base substitution C T upstream_gene_variant MELA-AU 4 153247560 153247562 deletion of <=200bp ATA - intron_variant MELA-AU 4 153247560 153247562 deletion of <=200bp ATA - upstream_gene_variant MELA-AU 4 153247568 153247568 single base substitution G A intron_variant MELA-AU 4 153247568 153247568 single base substitution G A upstream_gene_variant MELA-AU 4 153247872 153247872 single base substitution C T intron_variant MELA-AU 4 153247872 153247872 single base substitution C T upstream_gene_variant MELA-AU 4 153248512 153248512 single base substitution G A intron_variant MELA-AU 4 153248512 153248512 single base substitution G A upstream_gene_variant MELA-AU 4 153249128 153249128 single base substitution G A intron_variant MELA-AU 4 153249128 153249128 single base substitution G A upstream_gene_variant MELA-AU 4 153249511 153249511 single base substitution C A exon_variant MELA-AU 4 153249511 153249511 single base substitution C A stop_gained G247* 739G>T MELA-AU 4 153249511 153249511 single base substitution C A stop_gained G305* 913G>T MELA-AU 4 153249511 153249511 single base substitution C A stop_gained G343* 1027G>T MELA-AU 4 153249511 153249511 single base substitution C A stop_gained G423* 1267G>T MELA-AU 4 153249511 153249511 single base substitution C A upstream_gene_variant MELA-AU 4 153250269 153250269 single base substitution C T intron_variant MELA-AU 4 153250269 153250269 single base substitution C T upstream_gene_variant MELA-AU 4 153252053 153252053 single base substitution T A intron_variant MELA-AU 4 153252053 153252053 single base substitution T A upstream_gene_variant MELA-AU 4 153253310 153253310 single base substitution G A intron_variant MELA-AU 4 153253310 153253310 single base substitution G A upstream_gene_variant MELA-AU 4 153253375 153253375 single base substitution C T intron_variant MELA-AU 4 153253375 153253375 single base substitution C T upstream_gene_variant MELA-AU 4 153254530 153254530 single base substitution C T intron_variant MELA-AU 4 153254530 153254530 single base substitution C T upstream_gene_variant MELA-AU 4 153254620 153254620 single base substitution G A intron_variant MELA-AU 4 153254620 153254620 single base substitution G A upstream_gene_variant MELA-AU 4 153254684 153254684 single base substitution C T intron_variant MELA-AU 4 153254684 153254684 single base substitution C T upstream_gene_variant MELA-AU 4 153255700 153255700 single base substitution C T intron_variant MELA-AU 4 153255700 153255700 single base substitution C T upstream_gene_variant MELA-AU 4 153256410 153256410 single base substitution G A intron_variant MELA-AU 4 153256410 153256410 single base substitution G A upstream_gene_variant MELA-AU 4 153256441 153256441 single base substitution C T intron_variant MELA-AU 4 153256441 153256441 single base substitution C T upstream_gene_variant MELA-AU 4 153257214 153257214 single base substitution T C intron_variant MELA-AU 4 153257214 153257214 single base substitution T C upstream_gene_variant MELA-AU 4 153257302 153257302 single base substitution G A intron_variant MELA-AU 4 153257302 153257302 single base substitution G A upstream_gene_variant MELA-AU 4 153257646 153257646 single base substitution G A intron_variant MELA-AU 4 153257646 153257646 single base substitution G A upstream_gene_variant MELA-AU 4 153258036 153258036 deletion of <=200bp A - intron_variant MELA-AU 4 153258036 153258036 deletion of <=200bp A - upstream_gene_variant MELA-AU 4 153258244 153258244 single base substitution G A intron_variant MELA-AU 4 153258244 153258244 single base substitution G A upstream_gene_variant MELA-AU 4 153259097 153259097 single base substitution G A intron_variant MELA-AU 4 153259438 153259438 single base substitution G A intron_variant MELA-AU 4 153260718 153260718 single base substitution C A intron_variant MELA-AU 4 153261852 153261852 single base substitution G A intron_variant MELA-AU 4 153261962 153261962 single base substitution G A intron_variant MELA-AU 4 153261962 153261963 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153262136 153262136 single base substitution G A intron_variant MELA-AU 4 153262637 153262637 single base substitution G A intron_variant MELA-AU 4 153263255 153263255 single base substitution C G downstream_gene_variant MELA-AU 4 153263255 153263255 single base substitution C G intron_variant MELA-AU 4 153263265 153263265 single base substitution G A downstream_gene_variant MELA-AU 4 153263265 153263265 single base substitution G A intron_variant MELA-AU 4 153263371 153263371 single base substitution T G downstream_gene_variant MELA-AU 4 153263371 153263371 single base substitution T G intron_variant MELA-AU 4 153264021 153264021 single base substitution G A downstream_gene_variant MELA-AU 4 153264021 153264021 single base substitution G A intron_variant MELA-AU 4 153264692 153264692 single base substitution G A downstream_gene_variant MELA-AU 4 153264692 153264692 single base substitution G A intron_variant MELA-AU 4 153265714 153265714 single base substitution G A downstream_gene_variant MELA-AU 4 153265714 153265714 single base substitution G A intron_variant MELA-AU 4 153266177 153266177 single base substitution G A downstream_gene_variant MELA-AU 4 153266177 153266177 single base substitution G A intron_variant MELA-AU 4 153266204 153266204 single base substitution G A downstream_gene_variant MELA-AU 4 153266204 153266204 single base substitution G A intron_variant MELA-AU 4 153266259 153266259 single base substitution G A downstream_gene_variant MELA-AU 4 153266259 153266259 single base substitution G A intron_variant MELA-AU 4 153266329 153266329 single base substitution G A downstream_gene_variant MELA-AU 4 153266329 153266329 single base substitution G A intron_variant MELA-AU 4 153266350 153266350 single base substitution G A downstream_gene_variant MELA-AU 4 153266350 153266350 single base substitution G A intron_variant MELA-AU 4 153267879 153267879 single base substitution G A downstream_gene_variant MELA-AU 4 153267879 153267879 single base substitution G A intron_variant MELA-AU 4 153269090 153269090 single base substitution G A intron_variant MELA-AU 4 153269484 153269484 single base substitution C T intron_variant MELA-AU 4 153269622 153269622 single base substitution G A intron_variant MELA-AU 4 153270124 153270124 single base substitution C T intron_variant MELA-AU 4 153270124 153270124 single base substitution C T upstream_gene_variant MELA-AU 4 153271233 153271233 single base substitution G A exon_variant MELA-AU 4 153271233 153271233 single base substitution G A missense_variant S102F 305C>T MELA-AU 4 153271233 153271233 single base substitution G A missense_variant S182F 545C>T MELA-AU 4 153271233 153271233 single base substitution G A missense_variant S64F 191C>T MELA-AU 4 153271233 153271233 single base substitution G A upstream_gene_variant MELA-AU 4 153271455 153271455 single base substitution G A intron_variant MELA-AU 4 153271455 153271455 single base substitution G A upstream_gene_variant MELA-AU 4 153271537 153271537 single base substitution A T intron_variant MELA-AU 4 153271537 153271537 single base substitution A T upstream_gene_variant MELA-AU 4 153271595 153271595 single base substitution G A intron_variant MELA-AU 4 153271595 153271595 single base substitution G A upstream_gene_variant MELA-AU 4 153271731 153271731 single base substitution A G intron_variant MELA-AU 4 153271731 153271731 single base substitution A G upstream_gene_variant MELA-AU 4 153272572 153272572 single base substitution T C intron_variant MELA-AU 4 153272572 153272572 single base substitution T C upstream_gene_variant MELA-AU 4 153272721 153272721 single base substitution G T intron_variant MELA-AU 4 153272721 153272721 single base substitution G T upstream_gene_variant MELA-AU 4 153274019 153274019 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 4 153274019 153274019 single base substitution T A intron_variant MELA-AU 4 153274019 153274019 single base substitution T A upstream_gene_variant MELA-AU 4 153274405 153274405 single base substitution G A intron_variant MELA-AU 4 153274405 153274405 single base substitution G A upstream_gene_variant MELA-AU 4 153275007 153275007 single base substitution A G intron_variant MELA-AU 4 153275007 153275007 single base substitution A G upstream_gene_variant MELA-AU 4 153275011 153275011 single base substitution T C intron_variant MELA-AU 4 153275011 153275011 single base substitution T C upstream_gene_variant MELA-AU 4 153275735 153275735 single base substitution G A intron_variant MELA-AU 4 153275735 153275735 single base substitution G A upstream_gene_variant MELA-AU 4 153275883 153275883 single base substitution G A intron_variant MELA-AU 4 153275883 153275883 single base substitution G A upstream_gene_variant MELA-AU 4 153276827 153276827 single base substitution G A intron_variant MELA-AU 4 153276827 153276827 single base substitution G A upstream_gene_variant MELA-AU 4 153276980 153276980 single base substitution G A intron_variant MELA-AU 4 153276980 153276980 single base substitution G A upstream_gene_variant MELA-AU 4 153277685 153277685 single base substitution G A intron_variant MELA-AU 4 153277685 153277685 single base substitution G A upstream_gene_variant MELA-AU 4 153277780 153277780 single base substitution C T intron_variant MELA-AU 4 153277780 153277780 single base substitution C T upstream_gene_variant MELA-AU 4 153278693 153278693 single base substitution G A intron_variant MELA-AU 4 153278693 153278693 single base substitution G A upstream_gene_variant MELA-AU 4 153279544 153279544 single base substitution C T intron_variant MELA-AU 4 153279610 153279610 single base substitution C T intron_variant MELA-AU 4 153279962 153279962 single base substitution G A intron_variant MELA-AU 4 153280117 153280117 single base substitution C T intron_variant MELA-AU 4 153280679 153280679 single base substitution T G intron_variant MELA-AU 4 153280806 153280806 single base substitution G A intron_variant MELA-AU 4 153281670 153281671 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153283363 153283363 single base substitution G A intron_variant MELA-AU 4 153283555 153283555 single base substitution A T intron_variant MELA-AU 4 153283665 153283665 deletion of <=200bp T - intron_variant MELA-AU 4 153283851 153283851 single base substitution G A intron_variant MELA-AU 4 153284691 153284691 single base substitution C G intron_variant MELA-AU 4 153285028 153285028 single base substitution G A intron_variant MELA-AU 4 153285029 153285029 single base substitution G A intron_variant MELA-AU 4 153286161 153286161 single base substitution G A intron_variant MELA-AU 4 153286835 153286835 single base substitution G A intron_variant MELA-AU 4 153287035 153287035 single base substitution T C intron_variant MELA-AU 4 153287890 153287890 single base substitution G A intron_variant MELA-AU 4 153288025 153288025 single base substitution A G intron_variant MELA-AU 4 153288130 153288130 single base substitution G A intron_variant MELA-AU 4 153288135 153288135 single base substitution G A intron_variant MELA-AU 4 153289047 153289047 single base substitution A T intron_variant MELA-AU 4 153289104 153289104 single base substitution G A intron_variant MELA-AU 4 153290693 153290693 single base substitution G A intron_variant MELA-AU 4 153291144 153291144 single base substitution C T intron_variant MELA-AU 4 153291336 153291336 single base substitution C T intron_variant MELA-AU 4 153291344 153291344 single base substitution C T intron_variant MELA-AU 4 153291350 153291350 single base substitution G A intron_variant MELA-AU 4 153293148 153293148 single base substitution A T intron_variant MELA-AU 4 153293285 153293285 single base substitution A T intron_variant MELA-AU 4 153294413 153294413 single base substitution G A intron_variant MELA-AU 4 153294719 153294719 single base substitution A T intron_variant MELA-AU 4 153295682 153295682 single base substitution G A intron_variant MELA-AU 4 153295957 153295957 single base substitution A G intron_variant MELA-AU 4 153296389 153296389 single base substitution A T intron_variant MELA-AU 4 153296457 153296457 deletion of <=200bp A - intron_variant MELA-AU 4 153297108 153297108 single base substitution G A intron_variant MELA-AU 4 153297882 153297882 single base substitution G A intron_variant MELA-AU 4 153298195 153298195 single base substitution C T intron_variant MELA-AU 4 153298277 153298277 single base substitution G A intron_variant MELA-AU 4 153298345 153298345 single base substitution G A intron_variant MELA-AU 4 153298485 153298485 single base substitution G A intron_variant MELA-AU 4 153298613 153298613 single base substitution C T intron_variant MELA-AU 4 153299826 153299826 single base substitution G A intron_variant MELA-AU 4 153299951 153299951 single base substitution G A intron_variant MELA-AU 4 153300719 153300719 single base substitution G A intron_variant MELA-AU 4 153300874 153300874 single base substitution G A intron_variant MELA-AU 4 153301077 153301077 single base substitution T A intron_variant MELA-AU 4 153301251 153301251 single base substitution G A intron_variant MELA-AU 4 153302148 153302148 single base substitution A G intron_variant MELA-AU 4 153302379 153302379 single base substitution G A intron_variant MELA-AU 4 153302383 153302383 single base substitution G A intron_variant MELA-AU 4 153302806 153302806 single base substitution A T intron_variant MELA-AU 4 153303198 153303198 single base substitution T A intron_variant MELA-AU 4 153303256 153303256 single base substitution G A intron_variant MELA-AU 4 153303265 153303265 single base substitution G A intron_variant MELA-AU 4 153303285 153303286 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153303477 153303477 single base substitution G A intron_variant MELA-AU 4 153303477 153303477 single base substitution G A missense_variant P4L 11C>T MELA-AU 4 153303971 153303971 single base substitution G A intron_variant MELA-AU 4 153303971 153303971 single base substitution G A upstream_gene_variant MELA-AU 4 153304525 153304525 single base substitution C T intron_variant MELA-AU 4 153304525 153304525 single base substitution C T upstream_gene_variant MELA-AU 4 153304749 153304749 single base substitution C T intron_variant MELA-AU 4 153304749 153304749 single base substitution C T upstream_gene_variant MELA-AU 4 153304858 153304858 single base substitution A C intron_variant MELA-AU 4 153304858 153304858 single base substitution A C upstream_gene_variant MELA-AU 4 153305850 153305850 single base substitution A T intron_variant MELA-AU 4 153305850 153305850 single base substitution A T upstream_gene_variant MELA-AU 4 153306466 153306466 single base substitution G A intron_variant MELA-AU 4 153306466 153306466 single base substitution G A upstream_gene_variant MELA-AU 4 153306590 153306590 single base substitution G C intron_variant MELA-AU 4 153306590 153306590 single base substitution G C upstream_gene_variant MELA-AU 4 153306641 153306641 single base substitution G T intron_variant MELA-AU 4 153306641 153306641 single base substitution G T upstream_gene_variant MELA-AU 4 153307387 153307387 single base substitution G A intron_variant MELA-AU 4 153307387 153307387 single base substitution G A upstream_gene_variant MELA-AU 4 153308163 153308163 single base substitution A G intron_variant MELA-AU 4 153308163 153308163 single base substitution A G upstream_gene_variant MELA-AU 4 153308685 153308685 single base substitution G A intron_variant MELA-AU 4 153309888 153309888 single base substitution G A intron_variant MELA-AU 4 153310931 153310931 single base substitution T A intron_variant MELA-AU 4 153311441 153311441 single base substitution A T intron_variant MELA-AU 4 153311924 153311924 single base substitution G A intron_variant MELA-AU 4 153313574 153313574 single base substitution A G intron_variant MELA-AU 4 153313830 153313830 single base substitution T C intron_variant MELA-AU 4 153314012 153314012 single base substitution G A intron_variant MELA-AU 4 153314057 153314057 single base substitution A T intron_variant MELA-AU 4 153314060 153314060 single base substitution G A intron_variant MELA-AU 4 153314496 153314496 single base substitution G A intron_variant MELA-AU 4 153315234 153315234 single base substitution G A intron_variant MELA-AU 4 153315469 153315469 single base substitution G A intron_variant MELA-AU 4 153316690 153316690 single base substitution C T intron_variant MELA-AU 4 153316871 153316871 single base substitution C T intron_variant MELA-AU 4 153317979 153317979 single base substitution G A intron_variant MELA-AU 4 153318351 153318351 single base substitution T C intron_variant MELA-AU 4 153319887 153319888 multiple base substitution (>=2bp and <=200bp) GA AG intron_variant MELA-AU 4 153320098 153320098 single base substitution G A intron_variant MELA-AU 4 153320433 153320433 single base substitution G C intron_variant MELA-AU 4 153321323 153321323 single base substitution G A intron_variant MELA-AU 4 153321978 153321978 single base substitution G A intron_variant MELA-AU 4 153322036 153322036 single base substitution G A intron_variant MELA-AU 4 153322060 153322060 single base substitution G A intron_variant MELA-AU 4 153322063 153322063 single base substitution G A intron_variant MELA-AU 4 153322134 153322134 single base substitution A T intron_variant MELA-AU 4 153323086 153323086 single base substitution G A intron_variant MELA-AU 4 153323222 153323222 single base substitution G A intron_variant MELA-AU 4 153323519 153323519 single base substitution G A intron_variant MELA-AU 4 153323615 153323615 single base substitution G A intron_variant MELA-AU 4 153323726 153323726 single base substitution G A intron_variant MELA-AU 4 153323858 153323858 single base substitution G A intron_variant MELA-AU 4 153324395 153324395 single base substitution C T intron_variant MELA-AU 4 153324947 153324947 single base substitution C T intron_variant MELA-AU 4 153325372 153325372 single base substitution C T intron_variant MELA-AU 4 153326151 153326151 single base substitution G A intron_variant MELA-AU 4 153326520 153326520 single base substitution G A intron_variant MELA-AU 4 153326663 153326663 single base substitution G A intron_variant MELA-AU 4 153326994 153326994 single base substitution G A intron_variant MELA-AU 4 153327253 153327253 single base substitution G C intron_variant MELA-AU 4 153327411 153327411 single base substitution G A downstream_gene_variant MELA-AU 4 153327411 153327411 single base substitution G A intron_variant MELA-AU 4 153327479 153327479 single base substitution G A downstream_gene_variant MELA-AU 4 153327479 153327479 single base substitution G A intron_variant MELA-AU 4 153327511 153327511 single base substitution G A downstream_gene_variant MELA-AU 4 153327511 153327511 single base substitution G A intron_variant MELA-AU 4 153327572 153327572 single base substitution A C downstream_gene_variant MELA-AU 4 153327572 153327572 single base substitution A C intron_variant MELA-AU 4 153327743 153327743 single base substitution G A downstream_gene_variant MELA-AU 4 153327743 153327743 single base substitution G A intron_variant MELA-AU 4 153328132 153328132 single base substitution C T downstream_gene_variant MELA-AU 4 153328132 153328132 single base substitution C T intron_variant MELA-AU 4 153329199 153329199 single base substitution G A downstream_gene_variant MELA-AU 4 153329199 153329199 single base substitution G A intron_variant MELA-AU 4 153329225 153329225 single base substitution G A downstream_gene_variant MELA-AU 4 153329225 153329225 single base substitution G A intron_variant MELA-AU 4 153329245 153329245 single base substitution G A downstream_gene_variant MELA-AU 4 153329245 153329245 single base substitution G A intron_variant MELA-AU 4 153330101 153330101 single base substitution G A downstream_gene_variant MELA-AU 4 153330101 153330101 single base substitution G A intron_variant MELA-AU 4 153330256 153330256 single base substitution T A downstream_gene_variant MELA-AU 4 153330256 153330256 single base substitution T A intron_variant MELA-AU 4 153330594 153330594 single base substitution G A downstream_gene_variant MELA-AU 4 153330594 153330594 single base substitution G A intron_variant MELA-AU 4 153330693 153330693 single base substitution G A downstream_gene_variant MELA-AU 4 153330693 153330693 single base substitution G A intron_variant MELA-AU 4 153330707 153330707 single base substitution G A downstream_gene_variant MELA-AU 4 153330707 153330707 single base substitution G A intron_variant MELA-AU 4 153331129 153331129 single base substitution A T downstream_gene_variant MELA-AU 4 153331129 153331129 single base substitution A T intron_variant MELA-AU 4 153331283 153331283 single base substitution C T downstream_gene_variant MELA-AU 4 153331283 153331283 single base substitution C T intron_variant MELA-AU 4 153331569 153331569 single base substitution G A downstream_gene_variant MELA-AU 4 153331569 153331569 single base substitution G A intron_variant MELA-AU 4 153332141 153332141 single base substitution G A downstream_gene_variant MELA-AU 4 153332141 153332141 single base substitution G A intron_variant MELA-AU 4 153332668 153332668 single base substitution T C synonymous_variant E96E 288A>G MELA-AU 4 153332699 153332699 single base substitution G A missense_variant S86L 257C>T MELA-AU 4 153333093 153333093 single base substitution T C intron_variant MELA-AU 4 153333093 153333093 single base substitution T C upstream_gene_variant MELA-AU 4 153334226 153334226 single base substitution G A intron_variant MELA-AU 4 153334226 153334226 single base substitution G A upstream_gene_variant MELA-AU 4 153334429 153334429 single base substitution A G intron_variant MELA-AU 4 153334429 153334429 single base substitution A G upstream_gene_variant MELA-AU 4 153335339 153335339 single base substitution A C intron_variant MELA-AU 4 153335339 153335339 single base substitution A C upstream_gene_variant MELA-AU 4 153335654 153335654 single base substitution C T intron_variant MELA-AU 4 153335654 153335654 single base substitution C T upstream_gene_variant MELA-AU 4 153336968 153336968 single base substitution C T intron_variant MELA-AU 4 153336968 153336968 single base substitution C T upstream_gene_variant MELA-AU 4 153337253 153337253 single base substitution G A intron_variant MELA-AU 4 153337253 153337253 single base substitution G A upstream_gene_variant MELA-AU 4 153337726 153337726 single base substitution G A intron_variant MELA-AU 4 153337726 153337726 single base substitution G A upstream_gene_variant MELA-AU 4 153337759 153337759 single base substitution G A intron_variant MELA-AU 4 153337759 153337759 single base substitution G A upstream_gene_variant MELA-AU 4 153338044 153338044 single base substitution G A intron_variant MELA-AU 4 153338044 153338044 single base substitution G A upstream_gene_variant MELA-AU 4 153338582 153338582 single base substitution G A intron_variant MELA-AU 4 153338582 153338582 single base substitution G A upstream_gene_variant MELA-AU 4 153339518 153339518 single base substitution G A intron_variant MELA-AU 4 153340995 153340995 single base substitution G A intron_variant MELA-AU 4 153341106 153341106 single base substitution G A intron_variant MELA-AU 4 153341561 153341561 single base substitution C T intron_variant MELA-AU 4 153341733 153341733 single base substitution G A intron_variant MELA-AU 4 153342393 153342393 single base substitution A G intron_variant MELA-AU 4 153342721 153342721 single base substitution G A intron_variant MELA-AU 4 153342779 153342779 single base substitution C T intron_variant MELA-AU 4 153343674 153343674 single base substitution C T intron_variant MELA-AU 4 153344069 153344069 single base substitution G A intron_variant MELA-AU 4 153344878 153344878 single base substitution G A intron_variant MELA-AU 4 153344924 153344924 single base substitution G A intron_variant MELA-AU 4 153346295 153346295 single base substitution G A intron_variant MELA-AU 4 153346535 153346535 single base substitution G A intron_variant MELA-AU 4 153347417 153347417 single base substitution G A intron_variant MELA-AU 4 153347896 153347896 single base substitution G A intron_variant MELA-AU 4 153348044 153348044 single base substitution G A intron_variant MELA-AU 4 153348058 153348058 single base substitution G A intron_variant MELA-AU 4 153348169 153348169 single base substitution G A intron_variant MELA-AU 4 153348404 153348404 single base substitution T C intron_variant MELA-AU 4 153348723 153348723 single base substitution G A intron_variant MELA-AU 4 153349367 153349367 single base substitution T C intron_variant MELA-AU 4 153350040 153350040 single base substitution G A intron_variant MELA-AU 4 153352038 153352039 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153352538 153352538 single base substitution G A intron_variant MELA-AU 4 153352739 153352739 single base substitution C T intron_variant MELA-AU 4 153352862 153352862 single base substitution G A intron_variant MELA-AU 4 153353193 153353193 single base substitution C T intron_variant MELA-AU 4 153353470 153353471 multiple base substitution (>=2bp and <=200bp) GA AG intron_variant MELA-AU 4 153353521 153353521 single base substitution C T intron_variant MELA-AU 4 153353586 153353586 single base substitution G A intron_variant MELA-AU 4 153353707 153353707 single base substitution C G intron_variant MELA-AU 4 153353950 153353950 single base substitution C T intron_variant MELA-AU 4 153354101 153354101 single base substitution G A intron_variant MELA-AU 4 153354488 153354488 single base substitution G A intron_variant MELA-AU 4 153354699 153354699 single base substitution A T intron_variant MELA-AU 4 153354980 153354980 single base substitution G A intron_variant MELA-AU 4 153356685 153356685 single base substitution A T intron_variant MELA-AU 4 153357799 153357799 single base substitution G A intron_variant MELA-AU 4 153358251 153358251 single base substitution T C intron_variant MELA-AU 4 153358376 153358377 multiple base substitution (>=2bp and <=200bp) GT AC intron_variant MELA-AU 4 153359059 153359059 single base substitution G A intron_variant MELA-AU 4 153359360 153359360 single base substitution G A intron_variant MELA-AU 4 153360380 153360380 single base substitution C T intron_variant MELA-AU 4 153360505 153360505 single base substitution G A intron_variant MELA-AU 4 153360550 153360550 single base substitution T C intron_variant MELA-AU 4 153361699 153361699 single base substitution T C intron_variant MELA-AU 4 153362615 153362615 single base substitution G A intron_variant MELA-AU 4 153363080 153363080 single base substitution G A intron_variant MELA-AU 4 153363494 153363494 single base substitution G A intron_variant MELA-AU 4 153364486 153364486 single base substitution G A intron_variant MELA-AU 4 153364620 153364620 single base substitution A G intron_variant MELA-AU 4 153364863 153364863 single base substitution C T intron_variant MELA-AU 4 153365803 153365803 single base substitution A T intron_variant MELA-AU 4 153366293 153366293 single base substitution G A intron_variant MELA-AU 4 153366882 153366882 single base substitution G A intron_variant MELA-AU 4 153367439 153367439 single base substitution C A intron_variant MELA-AU 4 153367631 153367631 single base substitution G A intron_variant MELA-AU 4 153368081 153368081 single base substitution G A intron_variant MELA-AU 4 153368710 153368710 single base substitution G A intron_variant MELA-AU 4 153369218 153369233 deletion of <=200bp AAAACTTGAAACGAAG - intron_variant MELA-AU 4 153369230 153369230 single base substitution G A intron_variant MELA-AU 4 153369261 153369261 single base substitution C T intron_variant MELA-AU 4 153369389 153369389 single base substitution A G intron_variant MELA-AU 4 153369713 153369713 single base substitution G A intron_variant MELA-AU 4 153370282 153370282 single base substitution G A intron_variant MELA-AU 4 153370507 153370507 single base substitution G A intron_variant MELA-AU 4 153371314 153371314 single base substitution C T intron_variant MELA-AU 4 153371399 153371399 single base substitution A T intron_variant MELA-AU 4 153371804 153371804 single base substitution G A intron_variant MELA-AU 4 153372241 153372241 single base substitution G T intron_variant MELA-AU 4 153372736 153372736 single base substitution G A intron_variant MELA-AU 4 153373478 153373478 single base substitution A C intron_variant MELA-AU 4 153374143 153374143 single base substitution G A intron_variant MELA-AU 4 153374148 153374148 single base substitution A G intron_variant MELA-AU 4 153374535 153374535 single base substitution A C intron_variant MELA-AU 4 153374539 153374539 single base substitution C A intron_variant MELA-AU 4 153374706 153374706 single base substitution G A intron_variant MELA-AU 4 153374822 153374822 single base substitution G A intron_variant MELA-AU 4 153374834 153374834 single base substitution C T intron_variant MELA-AU 4 153375059 153375059 single base substitution G A intron_variant MELA-AU 4 153375167 153375167 single base substitution A G intron_variant MELA-AU 4 153375246 153375246 single base substitution G A intron_variant MELA-AU 4 153375309 153375309 deletion of <=200bp T - intron_variant MELA-AU 4 153375604 153375604 single base substitution C T intron_variant MELA-AU 4 153375760 153375760 single base substitution G A intron_variant MELA-AU 4 153375761 153375761 single base substitution G A intron_variant MELA-AU 4 153375912 153375912 single base substitution G A intron_variant MELA-AU 4 153377381 153377381 single base substitution A G intron_variant MELA-AU 4 153377598 153377598 single base substitution G A intron_variant MELA-AU 4 153377941 153377941 single base substitution G A intron_variant MELA-AU 4 153378243 153378243 single base substitution C T intron_variant MELA-AU 4 153378975 153378975 single base substitution T C intron_variant MELA-AU 4 153379011 153379011 single base substitution G A intron_variant MELA-AU 4 153379529 153379529 single base substitution G A intron_variant MELA-AU 4 153380684 153380684 single base substitution C G intron_variant MELA-AU 4 153380743 153380743 single base substitution G A intron_variant MELA-AU 4 153380773 153380773 single base substitution C T intron_variant MELA-AU 4 153380795 153380795 single base substitution C T intron_variant MELA-AU 4 153380819 153380819 single base substitution G A intron_variant MELA-AU 4 153381246 153381246 single base substitution T C intron_variant MELA-AU 4 153381354 153381354 single base substitution C T intron_variant MELA-AU 4 153381356 153381356 single base substitution T C intron_variant MELA-AU 4 153381528 153381528 single base substitution A T intron_variant MELA-AU 4 153382228 153382228 single base substitution G A intron_variant MELA-AU 4 153382456 153382456 single base substitution C T intron_variant MELA-AU 4 153382917 153382917 single base substitution G A intron_variant MELA-AU 4 153383602 153383602 single base substitution C T intron_variant MELA-AU 4 153383793 153383793 single base substitution G A intron_variant MELA-AU 4 153384556 153384556 single base substitution G A intron_variant MELA-AU 4 153384909 153384909 single base substitution C T intron_variant MELA-AU 4 153385647 153385647 single base substitution C T intron_variant MELA-AU 4 153386168 153386168 single base substitution G A intron_variant MELA-AU 4 153387379 153387379 single base substitution G A intron_variant MELA-AU 4 153387391 153387391 single base substitution G A intron_variant MELA-AU 4 153387470 153387470 single base substitution G A intron_variant MELA-AU 4 153387845 153387845 single base substitution A C intron_variant MELA-AU 4 153388038 153388038 single base substitution G A intron_variant MELA-AU 4 153388438 153388438 single base substitution C T intron_variant MELA-AU 4 153388612 153388612 single base substitution G C intron_variant MELA-AU 4 153388633 153388633 single base substitution G A intron_variant MELA-AU 4 153389003 153389003 single base substitution G A intron_variant MELA-AU 4 153389463 153389463 single base substitution T G intron_variant MELA-AU 4 153389999 153389999 single base substitution G A intron_variant MELA-AU 4 153390000 153390000 single base substitution G A intron_variant MELA-AU 4 153392508 153392508 single base substitution G A intron_variant MELA-AU 4 153392697 153392697 single base substitution A T intron_variant MELA-AU 4 153392889 153392889 single base substitution A G intron_variant MELA-AU 4 153393222 153393222 single base substitution G A intron_variant MELA-AU 4 153393365 153393365 single base substitution A T intron_variant MELA-AU 4 153393374 153393374 single base substitution G A intron_variant MELA-AU 4 153393398 153393398 single base substitution C T intron_variant MELA-AU 4 153393459 153393459 single base substitution G A intron_variant MELA-AU 4 153393494 153393494 single base substitution G A intron_variant MELA-AU 4 153393565 153393565 single base substitution G A intron_variant MELA-AU 4 153394711 153394711 single base substitution A C intron_variant MELA-AU 4 153395583 153395583 single base substitution G A intron_variant MELA-AU 4 153396033 153396033 single base substitution G A intron_variant MELA-AU 4 153396043 153396043 single base substitution C T intron_variant MELA-AU 4 153396250 153396250 single base substitution C T intron_variant MELA-AU 4 153396794 153396794 single base substitution G A intron_variant MELA-AU 4 153397380 153397380 single base substitution A T intron_variant MELA-AU 4 153397958 153397958 single base substitution G A intron_variant MELA-AU 4 153398467 153398467 single base substitution G A intron_variant MELA-AU 4 153399453 153399453 single base substitution T C intron_variant MELA-AU 4 153400231 153400231 single base substitution G A intron_variant MELA-AU 4 153400800 153400800 single base substitution G A intron_variant MELA-AU 4 153401168 153401168 single base substitution G A intron_variant MELA-AU 4 153401169 153401169 single base substitution G A intron_variant MELA-AU 4 153401629 153401629 single base substitution G A intron_variant MELA-AU 4 153403254 153403254 single base substitution A T intron_variant MELA-AU 4 153404514 153404514 single base substitution A T intron_variant MELA-AU 4 153404605 153404605 single base substitution C A intron_variant MELA-AU 4 153404671 153404671 single base substitution A G intron_variant MELA-AU 4 153405311 153405311 single base substitution T G intron_variant MELA-AU 4 153405570 153405570 single base substitution G A intron_variant MELA-AU 4 153405578 153405578 single base substitution G C intron_variant MELA-AU 4 153406298 153406298 single base substitution A C intron_variant MELA-AU 4 153406697 153406697 single base substitution C T intron_variant MELA-AU 4 153408446 153408446 single base substitution G A intron_variant MELA-AU 4 153409212 153409212 single base substitution C T intron_variant MELA-AU 4 153410391 153410391 single base substitution G A intron_variant MELA-AU 4 153411322 153411322 single base substitution G A intron_variant MELA-AU 4 153412880 153412880 single base substitution G A intron_variant MELA-AU 4 153413845 153413845 single base substitution G A intron_variant MELA-AU 4 153413853 153413853 single base substitution G A intron_variant MELA-AU 4 153413870 153413870 single base substitution G A intron_variant MELA-AU 4 153413907 153413907 single base substitution T G intron_variant MELA-AU 4 153415202 153415202 single base substitution A G intron_variant MELA-AU 4 153415561 153415561 single base substitution A G intron_variant MELA-AU 4 153416569 153416569 single base substitution G A intron_variant MELA-AU 4 153416598 153416598 single base substitution G A intron_variant MELA-AU 4 153416673 153416673 single base substitution G A intron_variant MELA-AU 4 153417651 153417651 single base substitution G A intron_variant MELA-AU 4 153417986 153417986 single base substitution G A intron_variant MELA-AU 4 153419450 153419450 single base substitution A G intron_variant MELA-AU 4 153420022 153420022 single base substitution G A intron_variant MELA-AU 4 153420541 153420541 single base substitution A T intron_variant MELA-AU 4 153420813 153420813 single base substitution G A intron_variant MELA-AU 4 153421507 153421507 single base substitution G A intron_variant MELA-AU 4 153421665 153421665 single base substitution A T intron_variant MELA-AU 4 153422593 153422593 single base substitution G A intron_variant MELA-AU 4 153423338 153423338 single base substitution T C intron_variant MELA-AU 4 153423726 153423726 single base substitution G A intron_variant MELA-AU 4 153424772 153424772 single base substitution A G intron_variant MELA-AU 4 153424812 153424812 single base substitution A C intron_variant MELA-AU 4 153425206 153425206 single base substitution G A intron_variant MELA-AU 4 153425807 153425807 single base substitution T C intron_variant MELA-AU 4 153425817 153425817 single base substitution G A intron_variant MELA-AU 4 153427308 153427308 single base substitution G A intron_variant MELA-AU 4 153428209 153428209 single base substitution C T intron_variant MELA-AU 4 153428402 153428402 single base substitution G A intron_variant MELA-AU 4 153428491 153428491 single base substitution G A intron_variant MELA-AU 4 153428547 153428547 single base substitution G A intron_variant MELA-AU 4 153428736 153428736 single base substitution T C intron_variant MELA-AU 4 153428979 153428979 single base substitution G A intron_variant MELA-AU 4 153429061 153429061 single base substitution G A intron_variant MELA-AU 4 153429260 153429260 single base substitution G A intron_variant MELA-AU 4 153429831 153429831 single base substitution A G intron_variant MELA-AU 4 153429885 153429885 single base substitution C T intron_variant MELA-AU 4 153430384 153430384 single base substitution A T intron_variant MELA-AU 4 153430470 153430470 single base substitution G A intron_variant MELA-AU 4 153430828 153430828 single base substitution G A intron_variant MELA-AU 4 153432307 153432307 single base substitution G A intron_variant MELA-AU 4 153432383 153432383 single base substitution G A intron_variant MELA-AU 4 153432855 153432855 single base substitution G A intron_variant MELA-AU 4 153433115 153433115 single base substitution A T intron_variant MELA-AU 4 153433445 153433445 single base substitution A G intron_variant MELA-AU 4 153433996 153433996 single base substitution G A intron_variant MELA-AU 4 153435377 153435377 single base substitution G A intron_variant MELA-AU 4 153435664 153435664 single base substitution G A intron_variant MELA-AU 4 153435813 153435813 single base substitution G A intron_variant MELA-AU 4 153438385 153438385 deletion of <=200bp T - intron_variant MELA-AU 4 153439059 153439060 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 153439704 153439704 single base substitution C T intron_variant MELA-AU 4 153439981 153439981 single base substitution G A intron_variant MELA-AU 4 153440268 153440268 single base substitution G A intron_variant MELA-AU 4 153440385 153440385 single base substitution G A intron_variant MELA-AU 4 153440475 153440475 single base substitution G T intron_variant MELA-AU 4 153440669 153440669 single base substitution C A intron_variant MELA-AU 4 153442000 153442000 single base substitution G A intron_variant MELA-AU 4 153442182 153442182 single base substitution G A intron_variant MELA-AU 4 153442312 153442312 deletion of <=200bp C - intron_variant MELA-AU 4 153442393 153442393 single base substitution A G intron_variant MELA-AU 4 153443074 153443074 single base substitution G A intron_variant MELA-AU 4 153443183 153443183 single base substitution G A intron_variant MELA-AU 4 153443252 153443252 single base substitution G A intron_variant MELA-AU 4 153443325 153443325 single base substitution C T intron_variant MELA-AU 4 153443857 153443857 single base substitution T A intron_variant MELA-AU 4 153444101 153444101 single base substitution G A intron_variant MELA-AU 4 153444310 153444310 single base substitution G A intron_variant MELA-AU 4 153444316 153444316 single base substitution G A intron_variant MELA-AU 4 153444613 153444613 single base substitution A T intron_variant MELA-AU 4 153445912 153445912 single base substitution G A intron_variant MELA-AU 4 153446737 153446737 single base substitution G A downstream_gene_variant MELA-AU 4 153446737 153446737 single base substitution G A intron_variant MELA-AU 4 153446980 153446980 single base substitution G A downstream_gene_variant MELA-AU 4 153446980 153446980 single base substitution G A intron_variant MELA-AU 4 153447895 153447895 single base substitution T C downstream_gene_variant MELA-AU 4 153447895 153447895 single base substitution T C intron_variant MELA-AU 4 153448597 153448597 single base substitution G A downstream_gene_variant MELA-AU 4 153448597 153448597 single base substitution G A intron_variant MELA-AU 4 153448682 153448683 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 153448682 153448683 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153448695 153448696 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 153448695 153448696 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153448988 153448988 single base substitution G A downstream_gene_variant MELA-AU 4 153448988 153448988 single base substitution G A intron_variant MELA-AU 4 153449063 153449063 single base substitution C T downstream_gene_variant MELA-AU 4 153449063 153449063 single base substitution C T intron_variant MELA-AU 4 153449346 153449346 single base substitution G A downstream_gene_variant MELA-AU 4 153449346 153449346 single base substitution G A intron_variant MELA-AU 4 153450124 153450124 single base substitution A C downstream_gene_variant MELA-AU 4 153450124 153450124 single base substitution A C intron_variant MELA-AU 4 153450443 153450443 single base substitution G A downstream_gene_variant MELA-AU 4 153450443 153450443 single base substitution G A intron_variant MELA-AU 4 153450552 153450552 single base substitution T C downstream_gene_variant MELA-AU 4 153450552 153450552 single base substitution T C intron_variant MELA-AU 4 153450877 153450878 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 153450877 153450878 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 153452128 153452128 single base substitution C T intron_variant MELA-AU 4 153452882 153452883 multiple base substitution (>=2bp and <=200bp) AG GA intron_variant MELA-AU 4 153453459 153453459 single base substitution G A intron_variant MELA-AU 4 153453468 153453468 single base substitution G A intron_variant MELA-AU 4 153454105 153454105 single base substitution G A intron_variant MELA-AU 4 153454200 153454200 single base substitution G A intron_variant MELA-AU 4 153454430 153454430 single base substitution A G intron_variant MELA-AU 4 153455118 153455118 single base substitution C T intron_variant MELA-AU 4 153456088 153456088 single base substitution C T intron_variant MELA-AU 4 153456088 153456088 single base substitution C T splice_region_variant MELA-AU 4 153456398 153456398 single base substitution G A 5_prime_UTR_variant MELA-AU 4 153456398 153456398 single base substitution G A upstream_gene_variant MELA-AU 4 153456502 153456502 single base substitution G A 5_prime_UTR_variant MELA-AU 4 153456502 153456502 single base substitution G A upstream_gene_variant MELA-AU 4 153456629 153456629 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 4 153456629 153456629 single base substitution G A upstream_gene_variant MELA-AU 4 153456638 153456638 single base substitution G A 5_prime_UTR_variant MELA-AU 4 153456638 153456638 single base substitution G A upstream_gene_variant MELA-AU 4 153457267 153457267 single base substitution C T upstream_gene_variant MELA-AU 4 153457310 153457311 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 4 153457317 153457317 single base substitution C T upstream_gene_variant MELA-AU 4 153457408 153457409 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 4 153457409 153457409 single base substitution G A upstream_gene_variant MELA-AU 4 153457410 153457410 single base substitution G A upstream_gene_variant MELA-AU 4 153457413 153457413 single base substitution G A upstream_gene_variant MELA-AU 4 153457815 153457815 single base substitution C T upstream_gene_variant MELA-AU 4 153459282 153459282 single base substitution G T upstream_gene_variant MELA-AU 4 153459614 153459614 single base substitution G A upstream_gene_variant MELA-AU 4 153459627 153459627 single base substitution G C upstream_gene_variant MELA-AU 4 153459815 153459815 single base substitution G C upstream_gene_variant MELA-AU 4 153460049 153460049 single base substitution G C upstream_gene_variant MELA-AU 4 153460296 153460296 single base substitution A G upstream_gene_variant MELA-AU 4 153460368 153460368 single base substitution C A upstream_gene_variant MELA-AU 4 153460677 153460677 single base substitution G C upstream_gene_variant MELA-AU 4 153460839 153460839 single base substitution C T upstream_gene_variant MELA-AU 4 153461250 153461250 single base substitution C T upstream_gene_variant MELA-AU 4 153461346 153461346 single base substitution C T upstream_gene_variant MELA-AU 4 153461425 153461425 single base substitution C T upstream_gene_variant MELA-AU 4 153461777 153461777 single base substitution C T upstream_gene_variant MELA-AU 4 153462114 153462114 single base substitution C T upstream_gene_variant MELA-AU 4 153462240 153462259 deletion of <=200bp CTCCAGGTCCTTGCTGGGCC - upstream_gene_variant ORCA-IN 4 153244080 153244080 single base substitution C T downstream_gene_variant ORCA-IN 4 153244080 153244080 single base substitution C T exon_variant ORCA-IN 4 153244080 153244080 single base substitution C T missense_variant E517K 1549G>A ORCA-IN 4 153244080 153244080 single base substitution C T missense_variant E575K 1723G>A ORCA-IN 4 153244080 153244080 single base substitution C T missense_variant E613K 1837G>A ORCA-IN 4 153244080 153244080 single base substitution C T missense_variant E693K 2077G>A ORCA-IN 4 153247487 153247487 deletion of <=200bp T - intron_variant ORCA-IN 4 153247487 153247487 deletion of <=200bp T - upstream_gene_variant ORCA-IN 4 153249384 153249384 single base substitution C T exon_variant ORCA-IN 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A ORCA-IN 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A ORCA-IN 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A ORCA-IN 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A ORCA-IN 4 153249384 153249384 single base substitution C T upstream_gene_variant ORCA-IN 4 153265686 153265686 deletion of <=200bp T - downstream_gene_variant ORCA-IN 4 153265686 153265686 deletion of <=200bp T - intron_variant ORCA-IN 4 153268228 153268228 deletion of <=200bp A - intron_variant ORCA-IN 4 153268228 153268228 deletion of <=200bp A - splice_region_variant ORCA-IN 4 153279664 153279664 deletion of <=200bp A - intron_variant ORCA-IN 4 153313424 153313424 single base substitution G C intron_variant ORCA-IN 4 153325689 153325689 single base substitution G C intron_variant ORCA-IN 4 153326247 153326247 insertion of <=200bp - A intron_variant ORCA-IN 4 153347522 153347522 single base substitution T A intron_variant ORCA-IN 4 153358530 153358530 insertion of <=200bp - A intron_variant ORCA-IN 4 153358531 153358531 deletion of <=200bp A - intron_variant ORCA-IN 4 153364273 153364273 single base substitution G T intron_variant ORCA-IN 4 153372936 153372936 deletion of <=200bp A - intron_variant ORCA-IN 4 153375404 153375404 deletion of <=200bp C - intron_variant ORCA-IN 4 153385391 153385391 single base substitution T C intron_variant ORCA-IN 4 153387707 153387707 deletion of <=200bp A - intron_variant ORCA-IN 4 153400389 153400389 single base substitution G A intron_variant ORCA-IN 4 153404552 153404552 deletion of <=200bp A - intron_variant ORCA-IN 4 153415258 153415258 single base substitution C T intron_variant ORCA-IN 4 153424432 153424432 deletion of <=200bp T - intron_variant ORCA-IN 4 153426895 153426895 insertion of <=200bp - TT intron_variant ORCA-IN 4 153426896 153426896 deletion of <=200bp T - intron_variant ORCA-IN 4 153429046 153429046 deletion of <=200bp A - intron_variant ORCA-IN 4 153429806 153429806 insertion of <=200bp - A intron_variant ORCA-IN 4 153432190 153432190 insertion of <=200bp - T intron_variant ORCA-IN 4 153436906 153436906 deletion of <=200bp T - intron_variant ORCA-IN 4 153449017 153449017 insertion of <=200bp - AC downstream_gene_variant ORCA-IN 4 153449017 153449017 insertion of <=200bp - AC intron_variant ORCA-IN 4 153449019 153449019 single base substitution C T downstream_gene_variant ORCA-IN 4 153449019 153449019 single base substitution C T intron_variant ORCA-IN 4 153452724 153452724 insertion of <=200bp - A intron_variant ORCA-IN 4 153452725 153452725 deletion of <=200bp A - intron_variant ORCA-IN 4 153452725 153452726 deletion of <=200bp AA - intron_variant ORCA-IN 4 153453023 153453023 deletion of <=200bp A - intron_variant ORCA-IN 4 153454341 153454341 insertion of <=200bp - A intron_variant ORCA-IN 4 153455408 153455408 insertion of <=200bp - A intron_variant ORCA-IN 4 153455409 153455409 deletion of <=200bp A - intron_variant OV-AU 4 153246802 153246802 single base substitution G A downstream_gene_variant OV-AU 4 153246802 153246802 single base substitution G A exon_variant OV-AU 4 153246802 153246802 single base substitution G A intron_variant OV-AU 4 153246802 153246802 single base substitution G A upstream_gene_variant OV-AU 4 153249206 153249206 single base substitution G A intron_variant OV-AU 4 153249206 153249206 single base substitution G A upstream_gene_variant OV-AU 4 153253865 153253865 single base substitution G C exon_variant OV-AU 4 153253865 153253865 single base substitution G C missense_variant L114V 340C>G OV-AU 4 153253865 153253865 single base substitution G C missense_variant L172V 514C>G OV-AU 4 153253865 153253865 single base substitution G C missense_variant L210V 628C>G OV-AU 4 153253865 153253865 single base substitution G C missense_variant L290V 868C>G OV-AU 4 153253865 153253865 single base substitution G C upstream_gene_variant OV-AU 4 153258411 153258411 single base substitution G C intron_variant OV-AU 4 153258411 153258411 single base substitution G C upstream_gene_variant OV-AU 4 153259520 153259520 single base substitution A G intron_variant OV-AU 4 153259645 153259645 single base substitution T A intron_variant OV-AU 4 153269301 153269301 single base substitution T A intron_variant OV-AU 4 153278507 153278507 single base substitution C G intron_variant OV-AU 4 153278507 153278507 single base substitution C G upstream_gene_variant OV-AU 4 153279905 153279905 single base substitution T A intron_variant OV-AU 4 153290624 153290624 single base substitution T C intron_variant OV-AU 4 153294132 153294132 single base substitution T C intron_variant OV-AU 4 153296275 153296275 single base substitution G T intron_variant OV-AU 4 153306031 153306031 single base substitution C T intron_variant OV-AU 4 153306031 153306031 single base substitution C T upstream_gene_variant OV-AU 4 153310394 153310394 single base substitution A G intron_variant OV-AU 4 153322081 153322081 single base substitution A G intron_variant OV-AU 4 153328035 153328035 single base substitution T C downstream_gene_variant OV-AU 4 153328035 153328035 single base substitution T C intron_variant OV-AU 4 153328964 153328964 single base substitution C T downstream_gene_variant OV-AU 4 153328964 153328964 single base substitution C T intron_variant OV-AU 4 153340422 153340422 single base substitution G A intron_variant OV-AU 4 153340446 153340446 single base substitution A C intron_variant OV-AU 4 153344237 153344237 single base substitution G C intron_variant OV-AU 4 153344559 153344559 single base substitution T A intron_variant OV-AU 4 153347619 153347619 single base substitution A C intron_variant OV-AU 4 153348115 153348115 single base substitution T A intron_variant OV-AU 4 153348134 153348134 single base substitution T A intron_variant OV-AU 4 153348181 153348181 single base substitution A G intron_variant OV-AU 4 153348183 153348183 single base substitution A G intron_variant OV-AU 4 153348185 153348185 single base substitution A G intron_variant OV-AU 4 153351783 153351783 single base substitution T G intron_variant OV-AU 4 153364698 153364698 single base substitution G C intron_variant OV-AU 4 153382598 153382598 single base substitution T A intron_variant OV-AU 4 153383865 153383865 single base substitution A C intron_variant OV-AU 4 153384406 153384406 single base substitution A C intron_variant OV-AU 4 153389943 153389943 single base substitution A C intron_variant OV-AU 4 153416233 153416233 single base substitution G T intron_variant OV-AU 4 153422551 153422551 single base substitution T A intron_variant OV-AU 4 153425107 153425107 single base substitution A T intron_variant OV-AU 4 153427352 153427352 single base substitution C A intron_variant OV-US 4 153247289 153247289 single base substitution G A downstream_gene_variant OV-US 4 153247289 153247289 single base substitution G A exon_variant OV-US 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T OV-US 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T OV-US 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T OV-US 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T OV-US 4 153247289 153247289 single base substitution G A upstream_gene_variant PACA-AU 4 153244772 153244772 deletion of <=200bp A - downstream_gene_variant PACA-AU 4 153244772 153244772 deletion of <=200bp A - exon_variant PACA-AU 4 153244772 153244772 deletion of <=200bp A - intron_variant PACA-AU 4 153245025 153245025 single base substitution A C downstream_gene_variant PACA-AU 4 153245025 153245025 single base substitution A C exon_variant PACA-AU 4 153245025 153245025 single base substitution A C intron_variant PACA-AU 4 153249440 153249440 single base substitution C A exon_variant PACA-AU 4 153249440 153249440 single base substitution C A missense_variant W270C 810G>T PACA-AU 4 153249440 153249440 single base substitution C A missense_variant W328C 984G>T PACA-AU 4 153249440 153249440 single base substitution C A missense_variant W366C 1098G>T PACA-AU 4 153249440 153249440 single base substitution C A missense_variant W446C 1338G>T PACA-AU 4 153249440 153249440 single base substitution C A upstream_gene_variant PACA-AU 4 153249465 153249465 single base substitution G T exon_variant PACA-AU 4 153249465 153249465 single base substitution G T missense_variant S262Y 785C>A PACA-AU 4 153249465 153249465 single base substitution G T missense_variant S320Y 959C>A PACA-AU 4 153249465 153249465 single base substitution G T missense_variant S358Y 1073C>A PACA-AU 4 153249465 153249465 single base substitution G T missense_variant S438Y 1313C>A PACA-AU 4 153249465 153249465 single base substitution G T upstream_gene_variant PACA-AU 4 153250525 153250525 deletion of <=200bp A - intron_variant PACA-AU 4 153250525 153250525 deletion of <=200bp A - upstream_gene_variant PACA-AU 4 153250882 153250882 single base substitution C T exon_variant PACA-AU 4 153250882 153250882 single base substitution C T missense_variant R217Q 650G>A PACA-AU 4 153250882 153250882 single base substitution C T missense_variant R275Q 824G>A PACA-AU 4 153250882 153250882 single base substitution C T missense_variant R313Q 938G>A PACA-AU 4 153250882 153250882 single base substitution C T missense_variant R393Q 1178G>A PACA-AU 4 153250882 153250882 single base substitution C T upstream_gene_variant PACA-AU 4 153251679 153251679 single base substitution C T intron_variant PACA-AU 4 153251679 153251679 single base substitution C T upstream_gene_variant PACA-AU 4 153251907 153251907 single base substitution G A exon_variant PACA-AU 4 153251907 153251907 single base substitution G A stop_gained R191* 571C>T PACA-AU 4 153251907 153251907 single base substitution G A stop_gained R249* 745C>T PACA-AU 4 153251907 153251907 single base substitution G A stop_gained R287* 859C>T PACA-AU 4 153251907 153251907 single base substitution G A stop_gained R367* 1099C>T PACA-AU 4 153251907 153251907 single base substitution G A upstream_gene_variant PACA-AU 4 153255391 153255391 single base substitution G T intron_variant PACA-AU 4 153255391 153255391 single base substitution G T upstream_gene_variant PACA-AU 4 153265919 153265919 single base substitution G A downstream_gene_variant PACA-AU 4 153265919 153265919 single base substitution G A intron_variant PACA-AU 4 153270900 153270900 single base substitution C A intron_variant PACA-AU 4 153270900 153270900 single base substitution C A upstream_gene_variant PACA-AU 4 153273602 153273602 single base substitution G A intron_variant PACA-AU 4 153273602 153273602 single base substitution G A upstream_gene_variant PACA-AU 4 153279560 153279560 single base substitution A T intron_variant PACA-AU 4 153288635 153288635 insertion of <=200bp - A intron_variant PACA-AU 4 153307081 153307081 deletion of <=200bp T - intron_variant PACA-AU 4 153307081 153307081 deletion of <=200bp T - upstream_gene_variant PACA-AU 4 153309431 153309431 single base substitution G T intron_variant PACA-AU 4 153319058 153319058 single base substitution G T intron_variant PACA-AU 4 153323611 153323611 single base substitution G A intron_variant PACA-AU 4 153339481 153339481 single base substitution G A intron_variant PACA-AU 4 153340650 153340650 single base substitution C A intron_variant PACA-AU 4 153348366 153348366 single base substitution G A intron_variant PACA-AU 4 153351479 153351479 single base substitution A C intron_variant PACA-AU 4 153359777 153359777 single base substitution A C intron_variant PACA-AU 4 153365979 153365979 single base substitution C A intron_variant PACA-AU 4 153368474 153368474 single base substitution T C intron_variant PACA-AU 4 153378932 153378932 single base substitution A T intron_variant PACA-AU 4 153379413 153379413 single base substitution G A intron_variant PACA-AU 4 153381082 153381082 single base substitution A C intron_variant PACA-AU 4 153386499 153386499 single base substitution A G intron_variant PACA-AU 4 153387868 153387868 single base substitution G A intron_variant PACA-AU 4 153393401 153393401 single base substitution C T intron_variant PACA-AU 4 153401401 153401401 single base substitution T C intron_variant PACA-AU 4 153417965 153417965 single base substitution A T intron_variant PACA-AU 4 153418087 153418087 single base substitution A G intron_variant PACA-AU 4 153422595 153422595 single base substitution A G intron_variant PACA-AU 4 153425990 153425990 single base substitution G T intron_variant PACA-AU 4 153428819 153428819 single base substitution G T intron_variant PACA-AU 4 153432483 153432483 single base substitution G T intron_variant PACA-AU 4 153436038 153436038 single base substitution G A intron_variant PACA-AU 4 153440452 153440455 deletion of <=200bp AAAT - intron_variant PACA-AU 4 153448585 153448585 deletion of <=200bp C - downstream_gene_variant PACA-AU 4 153448585 153448585 deletion of <=200bp C - intron_variant PACA-AU 4 153450384 153450384 single base substitution G C downstream_gene_variant PACA-AU 4 153450384 153450384 single base substitution G C intron_variant PACA-AU 4 153454930 153454930 single base substitution T G intron_variant PACA-AU 4 153460278 153460278 single base substitution C T upstream_gene_variant PACA-AU 4 153460895 153460895 single base substitution G A upstream_gene_variant PACA-AU 4 153461058 153461058 single base substitution G A upstream_gene_variant PACA-CA 4 153240528 153240528 single base substitution C A downstream_gene_variant PACA-CA 4 153241675 153241675 single base substitution G A downstream_gene_variant PACA-CA 4 153242064 153242064 single base substitution T C downstream_gene_variant PACA-CA 4 153244156 153244156 deletion of <=200bp C - downstream_gene_variant PACA-CA 4 153244156 153244156 deletion of <=200bp C - exon_variant PACA-CA 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G491 PACA-CA 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G549 PACA-CA 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G587 PACA-CA 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G667 PACA-CA 4 153245275 153245275 single base substitution T C downstream_gene_variant PACA-CA 4 153245275 153245275 single base substitution T C exon_variant PACA-CA 4 153245275 153245275 single base substitution T C intron_variant PACA-CA 4 153245501 153245501 single base substitution G A downstream_gene_variant PACA-CA 4 153245501 153245501 single base substitution G A exon_variant PACA-CA 4 153245501 153245501 single base substitution G A missense_variant R388C 1162C>T PACA-CA 4 153245501 153245501 single base substitution G A missense_variant R446C 1336C>T PACA-CA 4 153245501 153245501 single base substitution G A missense_variant R484C 1450C>T PACA-CA 4 153245501 153245501 single base substitution G A missense_variant R564C 1690C>T PACA-CA 4 153246227 153246227 single base substitution T C downstream_gene_variant PACA-CA 4 153246227 153246227 single base substitution T C exon_variant PACA-CA 4 153246227 153246227 single base substitution T C intron_variant PACA-CA 4 153246227 153246227 single base substitution T C upstream_gene_variant PACA-CA 4 153247289 153247289 single base substitution G A downstream_gene_variant PACA-CA 4 153247289 153247289 single base substitution G A exon_variant PACA-CA 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T PACA-CA 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T PACA-CA 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T PACA-CA 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T PACA-CA 4 153247289 153247289 single base substitution G A upstream_gene_variant PACA-CA 4 153247435 153247435 single base substitution G C intron_variant PACA-CA 4 153247435 153247435 single base substitution G C upstream_gene_variant PACA-CA 4 153248381 153248381 single base substitution C T intron_variant PACA-CA 4 153248381 153248381 single base substitution C T upstream_gene_variant PACA-CA 4 153248681 153248681 single base substitution A G intron_variant PACA-CA 4 153248681 153248681 single base substitution A G upstream_gene_variant PACA-CA 4 153252021 153252021 single base substitution C T splice_acceptor_variant PACA-CA 4 153252021 153252021 single base substitution C T upstream_gene_variant PACA-CA 4 153253262 153253262 deletion of <=200bp A - intron_variant PACA-CA 4 153253262 153253262 deletion of <=200bp A - upstream_gene_variant PACA-CA 4 153253293 153253293 single base substitution A C intron_variant PACA-CA 4 153253293 153253293 single base substitution A C upstream_gene_variant PACA-CA 4 153259037 153259037 single base substitution A G missense_variant C142R 424T>C PACA-CA 4 153259037 153259037 single base substitution A G missense_variant C180R 538T>C PACA-CA 4 153259037 153259037 single base substitution A G missense_variant C260R 778T>C PACA-CA 4 153259037 153259037 single base substitution A G missense_variant C84R 250T>C PACA-CA 4 153261843 153261843 single base substitution C T intron_variant PACA-CA 4 153263918 153263918 single base substitution A G downstream_gene_variant PACA-CA 4 153263918 153263918 single base substitution A G intron_variant PACA-CA 4 153268240 153268240 single base substitution A G intron_variant PACA-CA 4 153268993 153268993 deletion of <=200bp A - intron_variant PACA-CA 4 153274193 153274193 single base substitution C T intron_variant PACA-CA 4 153274193 153274193 single base substitution C T upstream_gene_variant PACA-CA 4 153275804 153275804 insertion of <=200bp - AA intron_variant PACA-CA 4 153275804 153275804 insertion of <=200bp - AA upstream_gene_variant PACA-CA 4 153276248 153276248 single base substitution G T intron_variant PACA-CA 4 153276248 153276248 single base substitution G T upstream_gene_variant PACA-CA 4 153278979 153278979 single base substitution A G intron_variant PACA-CA 4 153278979 153278979 single base substitution A G upstream_gene_variant PACA-CA 4 153289139 153289139 insertion of <=200bp - A intron_variant PACA-CA 4 153293002 153293002 single base substitution A T intron_variant PACA-CA 4 153294272 153294272 single base substitution G A intron_variant PACA-CA 4 153295186 153295186 deletion of <=200bp A - intron_variant PACA-CA 4 153296532 153296532 single base substitution T A intron_variant PACA-CA 4 153298145 153298145 single base substitution C T intron_variant PACA-CA 4 153312753 153312753 single base substitution G T intron_variant PACA-CA 4 153323251 153323251 single base substitution G A intron_variant PACA-CA 4 153326581 153326581 single base substitution G A intron_variant PACA-CA 4 153329087 153329087 single base substitution C T downstream_gene_variant PACA-CA 4 153329087 153329087 single base substitution C T intron_variant PACA-CA 4 153332404 153332404 single base substitution A C 3_prime_UTR_variant PACA-CA 4 153332404 153332404 single base substitution A C downstream_gene_variant PACA-CA 4 153332404 153332404 single base substitution A C intron_variant PACA-CA 4 153339874 153339874 single base substitution C T intron_variant PACA-CA 4 153344054 153344054 single base substitution C G intron_variant PACA-CA 4 153347765 153347765 single base substitution G A intron_variant PACA-CA 4 153347811 153347811 single base substitution C G intron_variant PACA-CA 4 153358991 153358991 single base substitution A C intron_variant PACA-CA 4 153364169 153364169 deletion of <=200bp C - intron_variant PACA-CA 4 153367016 153367016 single base substitution C T intron_variant PACA-CA 4 153378059 153378059 single base substitution C G intron_variant PACA-CA 4 153379467 153379467 single base substitution G A intron_variant PACA-CA 4 153381174 153381174 single base substitution A G intron_variant PACA-CA 4 153382190 153382190 single base substitution T C intron_variant PACA-CA 4 153382426 153382426 single base substitution T A intron_variant PACA-CA 4 153383420 153383433 deletion of <=200bp CTCTGATACCTCAA - intron_variant PACA-CA 4 153384148 153384148 single base substitution G A intron_variant PACA-CA 4 153387505 153387505 single base substitution G A intron_variant PACA-CA 4 153387808 153387808 single base substitution A T intron_variant PACA-CA 4 153393515 153393515 single base substitution A T intron_variant PACA-CA 4 153397259 153397259 single base substitution A G intron_variant PACA-CA 4 153399825 153399825 single base substitution G A intron_variant PACA-CA 4 153403239 153403239 single base substitution G T intron_variant PACA-CA 4 153404402 153404402 single base substitution G T intron_variant PACA-CA 4 153404850 153404850 insertion of <=200bp - A intron_variant PACA-CA 4 153406573 153406573 single base substitution G A intron_variant PACA-CA 4 153408259 153408259 single base substitution A G intron_variant PACA-CA 4 153412758 153412758 single base substitution A G intron_variant PACA-CA 4 153418801 153418801 single base substitution A G intron_variant PACA-CA 4 153420644 153420644 single base substitution A G intron_variant PACA-CA 4 153425540 153425540 insertion of <=200bp - A intron_variant PACA-CA 4 153429819 153429819 single base substitution G A intron_variant PACA-CA 4 153430902 153430902 single base substitution G T intron_variant PACA-CA 4 153431287 153431287 single base substitution T A intron_variant PACA-CA 4 153434287 153434287 single base substitution A G intron_variant PACA-CA 4 153435900 153435900 single base substitution G A intron_variant PACA-CA 4 153436599 153436599 deletion of <=200bp A - intron_variant PACA-CA 4 153437008 153437008 single base substitution G C intron_variant PACA-CA 4 153437269 153437269 single base substitution G C intron_variant PACA-CA 4 153438443 153438443 single base substitution C T intron_variant PACA-CA 4 153438455 153438455 single base substitution C T intron_variant PACA-CA 4 153439147 153439147 single base substitution C T intron_variant PACA-CA 4 153440475 153440475 single base substitution G T intron_variant PACA-CA 4 153444420 153444420 single base substitution C A intron_variant PACA-CA 4 153444603 153444603 single base substitution C A intron_variant PACA-CA 4 153451274 153451274 insertion of <=200bp - AT downstream_gene_variant PACA-CA 4 153451274 153451274 insertion of <=200bp - AT intron_variant PACA-CA 4 153454940 153454940 single base substitution A T intron_variant PACA-CA 4 153455672 153455672 single base substitution G T intron_variant PACA-CA 4 153458809 153458810 deletion of <=200bp CT - upstream_gene_variant PACA-CA 4 153459744 153459744 single base substitution A G upstream_gene_variant PACA-CA 4 153462038 153462038 single base substitution G A upstream_gene_variant PAEN-AU 4 153283049 153283049 single base substitution T G intron_variant PAEN-AU 4 153310676 153310676 single base substitution C A intron_variant PAEN-AU 4 153311171 153311171 single base substitution T A intron_variant PAEN-AU 4 153312446 153312446 single base substitution T C intron_variant PAEN-AU 4 153334260 153334260 single base substitution T C intron_variant PAEN-AU 4 153334260 153334260 single base substitution T C upstream_gene_variant PAEN-AU 4 153350549 153350549 single base substitution A G intron_variant PAEN-AU 4 153379386 153379386 single base substitution G A intron_variant PAEN-AU 4 153390500 153390501 deletion of <=200bp TC - intron_variant PAEN-AU 4 153418397 153418397 single base substitution C A intron_variant PAEN-AU 4 153420856 153420856 single base substitution T C intron_variant PAEN-AU 4 153448516 153448516 single base substitution C T downstream_gene_variant PAEN-AU 4 153448516 153448516 single base substitution C T intron_variant PAEN-AU 4 153453741 153453749 deletion of <=200bp ACTTGCTCT - intron_variant PAEN-IT 4 153245974 153245974 single base substitution G C downstream_gene_variant PAEN-IT 4 153245974 153245974 single base substitution G C exon_variant PAEN-IT 4 153245974 153245974 single base substitution G C intron_variant PAEN-IT 4 153245974 153245974 single base substitution G C upstream_gene_variant PAEN-IT 4 153276657 153276657 single base substitution T C intron_variant PAEN-IT 4 153276657 153276657 single base substitution T C upstream_gene_variant PAEN-IT 4 153286788 153286788 single base substitution C A intron_variant PAEN-IT 4 153314402 153314402 single base substitution C A intron_variant PAEN-IT 4 153315841 153315841 single base substitution A C intron_variant PAEN-IT 4 153402648 153402648 single base substitution T C intron_variant PAEN-IT 4 153425744 153425744 single base substitution G T intron_variant PAEN-IT 4 153434840 153434840 single base substitution A G intron_variant PAEN-IT 4 153453114 153453114 single base substitution C T intron_variant PBCA-DE 4 153244097 153244097 single base substitution C T downstream_gene_variant PBCA-DE 4 153244097 153244097 single base substitution C T exon_variant PBCA-DE 4 153244097 153244097 single base substitution C T missense_variant G511E 1532G>A PBCA-DE 4 153244097 153244097 single base substitution C T missense_variant G569E 1706G>A PBCA-DE 4 153244097 153244097 single base substitution C T missense_variant G607E 1820G>A PBCA-DE 4 153244097 153244097 single base substitution C T missense_variant G687E 2060G>A PBCA-DE 4 153245357 153245357 single base substitution G A downstream_gene_variant PBCA-DE 4 153245357 153245357 single base substitution G A exon_variant PBCA-DE 4 153245357 153245357 single base substitution G A stop_gained Q436* 1306C>T PBCA-DE 4 153245357 153245357 single base substitution G A stop_gained Q494* 1480C>T PBCA-DE 4 153245357 153245357 single base substitution G A stop_gained Q532* 1594C>T PBCA-DE 4 153245357 153245357 single base substitution G A stop_gained Q612* 1834C>T PBCA-DE 4 153247366 153247366 single base substitution C T downstream_gene_variant PBCA-DE 4 153247366 153247366 single base substitution C T exon_variant PBCA-DE 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A PBCA-DE 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A PBCA-DE 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A PBCA-DE 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A PBCA-DE 4 153247366 153247366 single base substitution C T upstream_gene_variant PBCA-DE 4 153249385 153249385 single base substitution G A exon_variant PBCA-DE 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T PBCA-DE 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T PBCA-DE 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T PBCA-DE 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T PBCA-DE 4 153249385 153249385 single base substitution G A upstream_gene_variant PBCA-DE 4 153250900 153250900 single base substitution A T exon_variant PBCA-DE 4 153250900 153250900 single base substitution A T stop_gained L211* 632T>A PBCA-DE 4 153250900 153250900 single base substitution A T stop_gained L269* 806T>A PBCA-DE 4 153250900 153250900 single base substitution A T stop_gained L307* 920T>A PBCA-DE 4 153250900 153250900 single base substitution A T stop_gained L387* 1160T>A PBCA-DE 4 153250900 153250900 single base substitution A T upstream_gene_variant PBCA-DE 4 153255065 153255065 insertion of <=200bp - A intron_variant PBCA-DE 4 153255065 153255065 insertion of <=200bp - A upstream_gene_variant PBCA-DE 4 153255067 153255070 deletion of <=200bp GTGG - intron_variant PBCA-DE 4 153255067 153255070 deletion of <=200bp GTGG - upstream_gene_variant PBCA-DE 4 153258983 153258983 single base substitution G A stop_gained R102* 304C>T PBCA-DE 4 153258983 153258983 single base substitution G A stop_gained R160* 478C>T PBCA-DE 4 153258983 153258983 single base substitution G A stop_gained R198* 592C>T PBCA-DE 4 153258983 153258983 single base substitution G A stop_gained R278* 832C>T PBCA-DE 4 153261656 153261656 single base substitution G A intron_variant PBCA-DE 4 153268081 153268081 single base substitution C T exon_variant PBCA-DE 4 153268081 153268081 single base substitution C T splice_donor_variant PBCA-DE 4 153290748 153290748 single base substitution G A intron_variant PBCA-DE 4 153292441 153292441 single base substitution A T intron_variant PBCA-DE 4 153313833 153313833 single base substitution C G intron_variant PBCA-DE 4 153319486 153319486 insertion of <=200bp - A intron_variant PBCA-DE 4 153322764 153322764 single base substitution C T intron_variant PBCA-DE 4 153338251 153338251 single base substitution C T intron_variant PBCA-DE 4 153338251 153338251 single base substitution C T upstream_gene_variant PBCA-DE 4 153339280 153339281 deletion of <=200bp CA - intron_variant PBCA-DE 4 153349502 153349502 single base substitution C T intron_variant PBCA-DE 4 153353433 153353433 single base substitution A G intron_variant PBCA-DE 4 153362064 153362064 single base substitution C T intron_variant PBCA-DE 4 153367016 153367020 deletion of <=200bp CGCGC - intron_variant PBCA-DE 4 153375715 153375715 insertion of <=200bp - A intron_variant PBCA-DE 4 153376548 153376548 single base substitution C A intron_variant PBCA-DE 4 153384723 153384723 insertion of <=200bp - A intron_variant PBCA-DE 4 153384896 153384896 single base substitution A T intron_variant PBCA-DE 4 153388657 153388657 deletion of <=200bp A - intron_variant PBCA-DE 4 153398704 153398704 insertion of <=200bp - A intron_variant PBCA-DE 4 153401169 153401169 single base substitution G A intron_variant PBCA-DE 4 153404532 153404532 single base substitution A T intron_variant PBCA-DE 4 153412861 153412861 insertion of <=200bp - C intron_variant PBCA-DE 4 153414564 153414564 single base substitution G A intron_variant PBCA-DE 4 153426345 153426345 single base substitution C T intron_variant PBCA-DE 4 153429414 153429414 single base substitution G A intron_variant PBCA-DE 4 153438664 153438664 single base substitution C T intron_variant PBCA-DE 4 153438909 153438909 single base substitution G A intron_variant PBCA-DE 4 153440105 153440105 single base substitution A T intron_variant PBCA-DE 4 153440860 153440860 single base substitution C A intron_variant PBCA-DE 4 153445846 153445846 single base substitution A G intron_variant PBCA-DE 4 153446488 153446488 single base substitution C T downstream_gene_variant PBCA-DE 4 153446488 153446488 single base substitution C T intron_variant PBCA-DE 4 153452213 153452214 deletion of <=200bp AC - intron_variant PRAD-CA 4 153263656 153263656 single base substitution T C downstream_gene_variant PRAD-CA 4 153263656 153263656 single base substitution T C intron_variant PRAD-CA 4 153268131 153268131 single base substitution G A exon_variant PRAD-CA 4 153268131 153268131 single base substitution G A missense_variant T108I 323C>T PRAD-CA 4 153268131 153268131 single base substitution G A missense_variant T146I 437C>T PRAD-CA 4 153268131 153268131 single base substitution G A missense_variant T226I 677C>T PRAD-CA 4 153268131 153268131 single base substitution G A missense_variant T50I 149C>T PRAD-CA 4 153272648 153272648 single base substitution T C intron_variant PRAD-CA 4 153272648 153272648 single base substitution T C upstream_gene_variant PRAD-CA 4 153292677 153292677 single base substitution C G intron_variant PRAD-CA 4 153297841 153297841 single base substitution G A intron_variant PRAD-CA 4 153333100 153333100 single base substitution T A intron_variant PRAD-CA 4 153333100 153333100 single base substitution T A upstream_gene_variant PRAD-CA 4 153345383 153345383 single base substitution A T intron_variant PRAD-CA 4 153427139 153427139 single base substitution C G intron_variant PRAD-CA 4 153429482 153429482 single base substitution A C intron_variant PRAD-CA 4 153429819 153429819 single base substitution G A intron_variant PRAD-CA 4 153451222 153451222 single base substitution T A downstream_gene_variant PRAD-CA 4 153451222 153451222 single base substitution T A intron_variant PRAD-CA 4 153457496 153457496 single base substitution C T upstream_gene_variant PRAD-CA 4 153462038 153462038 single base substitution G C upstream_gene_variant PRAD-UK 4 153260931 153260931 insertion of <=200bp - A intron_variant PRAD-UK 4 153280585 153280585 single base substitution T C intron_variant PRAD-UK 4 153292280 153292280 single base substitution G C intron_variant PRAD-UK 4 153304035 153304035 single base substitution A T intron_variant PRAD-UK 4 153304035 153304035 single base substitution A T upstream_gene_variant PRAD-UK 4 153304037 153304037 single base substitution A C intron_variant PRAD-UK 4 153304037 153304037 single base substitution A C upstream_gene_variant PRAD-UK 4 153304040 153304040 deletion of <=200bp A - intron_variant PRAD-UK 4 153304040 153304040 deletion of <=200bp A - upstream_gene_variant PRAD-UK 4 153306078 153306078 single base substitution A C intron_variant PRAD-UK 4 153306078 153306078 single base substitution A C upstream_gene_variant PRAD-UK 4 153342602 153342602 single base substitution C T intron_variant PRAD-UK 4 153347041 153347041 single base substitution G A intron_variant PRAD-UK 4 153357411 153357411 single base substitution G T intron_variant PRAD-UK 4 153358075 153358075 single base substitution C A intron_variant PRAD-UK 4 153365288 153365288 single base substitution C T intron_variant PRAD-UK 4 153366985 153366985 single base substitution C T intron_variant PRAD-UK 4 153390663 153390663 single base substitution C A intron_variant PRAD-UK 4 153391809 153391809 single base substitution G T intron_variant PRAD-UK 4 153392379 153392379 single base substitution A T intron_variant PRAD-UK 4 153394839 153394842 multiple base substitution (>=2bp and <=200bp) TTGC TAT intron_variant PRAD-UK 4 153411530 153411530 single base substitution T A intron_variant PRAD-UK 4 153413062 153413062 single base substitution A G intron_variant PRAD-UK 4 153421035 153421035 single base substitution G A intron_variant PRAD-UK 4 153424342 153424342 single base substitution G A intron_variant PRAD-UK 4 153428613 153428613 single base substitution C A intron_variant PRAD-UK 4 153438799 153438799 single base substitution A T intron_variant PRAD-UK 4 153441094 153441094 single base substitution G C intron_variant PRAD-UK 4 153449937 153449937 deletion of <=200bp C - downstream_gene_variant PRAD-UK 4 153449937 153449937 deletion of <=200bp C - intron_variant PRAD-UK 4 153461904 153461904 single base substitution T C upstream_gene_variant READ-US 4 153244185 153244185 single base substitution G A downstream_gene_variant READ-US 4 153244185 153244185 single base substitution G A exon_variant READ-US 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T READ-US 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T READ-US 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T READ-US 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T READ-US 4 153245446 153245446 single base substitution G A downstream_gene_variant READ-US 4 153245446 153245446 single base substitution G A exon_variant READ-US 4 153245446 153245446 single base substitution G A missense_variant S406L 1217C>T READ-US 4 153245446 153245446 single base substitution G A missense_variant S464L 1391C>T READ-US 4 153245446 153245446 single base substitution G A missense_variant S502L 1505C>T READ-US 4 153245446 153245446 single base substitution G A missense_variant S582L 1745C>T READ-US 4 153247367 153247367 single base substitution G A downstream_gene_variant READ-US 4 153247367 153247367 single base substitution G A exon_variant READ-US 4 153247367 153247367 single base substitution G A stop_gained R303* 907C>T READ-US 4 153247367 153247367 single base substitution G A stop_gained R361* 1081C>T READ-US 4 153247367 153247367 single base substitution G A stop_gained R399* 1195C>T READ-US 4 153247367 153247367 single base substitution G A stop_gained R479* 1435C>T READ-US 4 153247367 153247367 single base substitution G A upstream_gene_variant READ-US 4 153249360 153249360 insertion of <=200bp - T frameshift_variant R297R? READ-US 4 153249360 153249360 insertion of <=200bp - T frameshift_variant R355R? READ-US 4 153249360 153249360 insertion of <=200bp - T frameshift_variant R393R? READ-US 4 153249360 153249360 insertion of <=200bp - T frameshift_variant R473R? READ-US 4 153249360 153249360 insertion of <=200bp - T splice_region_variant READ-US 4 153249360 153249360 insertion of <=200bp - T upstream_gene_variant READ-US 4 153249384 153249384 single base substitution C T exon_variant READ-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A READ-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A READ-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A READ-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A READ-US 4 153249384 153249384 single base substitution C T upstream_gene_variant READ-US 4 153249385 153249385 single base substitution G A exon_variant READ-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T READ-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T READ-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T READ-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T READ-US 4 153249385 153249385 single base substitution G A upstream_gene_variant READ-US 4 153251907 153251907 single base substitution G A exon_variant READ-US 4 153251907 153251907 single base substitution G A stop_gained R191* 571C>T READ-US 4 153251907 153251907 single base substitution G A stop_gained R249* 745C>T READ-US 4 153251907 153251907 single base substitution G A stop_gained R287* 859C>T READ-US 4 153251907 153251907 single base substitution G A stop_gained R367* 1099C>T READ-US 4 153251907 153251907 single base substitution G A upstream_gene_variant READ-US 4 153258970 153258970 single base substitution G T stop_gained S106* 317C>A READ-US 4 153258970 153258970 single base substitution G T stop_gained S164* 491C>A READ-US 4 153258970 153258970 single base substitution G T stop_gained S202* 605C>A READ-US 4 153258970 153258970 single base substitution G T stop_gained S282* 845C>A READ-US 4 153268138 153268138 single base substitution G A exon_variant READ-US 4 153268138 153268138 single base substitution G A stop_gained R106* 316C>T READ-US 4 153268138 153268138 single base substitution G A stop_gained R144* 430C>T READ-US 4 153268138 153268138 single base substitution G A stop_gained R224* 670C>T READ-US 4 153268138 153268138 single base substitution G A stop_gained R48* 142C>T READ-US 4 153332667 153332667 single base substitution C A stop_gained E97* 289G>T RECA-EU 4 153245762 153245762 single base substitution T G downstream_gene_variant RECA-EU 4 153245762 153245762 single base substitution T G exon_variant RECA-EU 4 153245762 153245762 single base substitution T G intron_variant RECA-EU 4 153245762 153245762 single base substitution T G upstream_gene_variant RECA-EU 4 153263316 153263316 single base substitution T C downstream_gene_variant RECA-EU 4 153263316 153263316 single base substitution T C intron_variant RECA-EU 4 153272284 153272284 single base substitution T A intron_variant RECA-EU 4 153272284 153272284 single base substitution T A upstream_gene_variant RECA-EU 4 153274511 153274511 single base substitution C G intron_variant RECA-EU 4 153274511 153274511 single base substitution C G upstream_gene_variant RECA-EU 4 153283203 153283203 single base substitution A C intron_variant RECA-EU 4 153294019 153294019 single base substitution A T intron_variant RECA-EU 4 153320117 153320117 single base substitution T C intron_variant RECA-EU 4 153320728 153320728 single base substitution A C intron_variant RECA-EU 4 153322222 153322222 single base substitution G A intron_variant RECA-EU 4 153334093 153334093 single base substitution A T intron_variant RECA-EU 4 153334093 153334093 single base substitution A T upstream_gene_variant RECA-EU 4 153347813 153347813 single base substitution G A intron_variant RECA-EU 4 153355650 153355650 single base substitution A G intron_variant RECA-EU 4 153374526 153374526 single base substitution C G intron_variant RECA-EU 4 153374997 153374997 single base substitution C A intron_variant RECA-EU 4 153392128 153392128 single base substitution T A intron_variant RECA-EU 4 153408038 153408038 single base substitution A G intron_variant RECA-EU 4 153419538 153419538 single base substitution C A intron_variant RECA-EU 4 153420208 153420208 single base substitution C T intron_variant RECA-EU 4 153421913 153421913 single base substitution C A intron_variant RECA-EU 4 153426927 153426927 single base substitution T A intron_variant RECA-EU 4 153430263 153430263 single base substitution A T intron_variant RECA-EU 4 153442615 153442615 single base substitution A G intron_variant RECA-EU 4 153450975 153450975 single base substitution A C downstream_gene_variant RECA-EU 4 153450975 153450975 single base substitution A C intron_variant RECA-EU 4 153457602 153457602 single base substitution T C upstream_gene_variant RECA-EU 4 153458287 153458287 single base substitution G C upstream_gene_variant RECA-EU 4 153461841 153461841 single base substitution A C upstream_gene_variant SKCA-BR 4 153237578 153237578 single base substitution G A downstream_gene_variant SKCA-BR 4 153239417 153239417 single base substitution G A downstream_gene_variant SKCA-BR 4 153241639 153241639 single base substitution A G downstream_gene_variant SKCA-BR 4 153243476 153243476 insertion of <=200bp - CA 3_prime_UTR_variant SKCA-BR 4 153243476 153243476 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 4 153243876 153243876 single base substitution A G 3_prime_UTR_variant SKCA-BR 4 153243876 153243876 single base substitution A G downstream_gene_variant SKCA-BR 4 153245534 153245534 single base substitution G A downstream_gene_variant SKCA-BR 4 153245534 153245534 single base substitution G A exon_variant SKCA-BR 4 153245534 153245534 single base substitution G A missense_variant H377Y 1129C>T SKCA-BR 4 153245534 153245534 single base substitution G A missense_variant H435Y 1303C>T SKCA-BR 4 153245534 153245534 single base substitution G A missense_variant H473Y 1417C>T SKCA-BR 4 153245534 153245534 single base substitution G A missense_variant H553Y 1657C>T SKCA-BR 4 153247486 153247486 insertion of <=200bp - CT intron_variant SKCA-BR 4 153247486 153247486 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 4 153264529 153264529 single base substitution G A downstream_gene_variant SKCA-BR 4 153264529 153264529 single base substitution G A intron_variant SKCA-BR 4 153265451 153265451 single base substitution G A downstream_gene_variant SKCA-BR 4 153265451 153265451 single base substitution G A intron_variant SKCA-BR 4 153266776 153266776 single base substitution C T downstream_gene_variant SKCA-BR 4 153266776 153266776 single base substitution C T intron_variant SKCA-BR 4 153280119 153280124 deletion of <=200bp CAAGTT - intron_variant SKCA-BR 4 153280806 153280806 single base substitution G A intron_variant SKCA-BR 4 153287303 153287311 deletion of <=200bp TTATAATTA - intron_variant SKCA-BR 4 153288146 153288146 single base substitution G A intron_variant SKCA-BR 4 153288393 153288393 single base substitution G A intron_variant SKCA-BR 4 153294361 153294361 single base substitution G A intron_variant SKCA-BR 4 153295130 153295130 single base substitution A G intron_variant SKCA-BR 4 153296015 153296015 single base substitution G A intron_variant SKCA-BR 4 153299313 153299313 single base substitution G A intron_variant SKCA-BR 4 153300862 153300862 single base substitution G A intron_variant SKCA-BR 4 153302241 153302241 single base substitution A C intron_variant SKCA-BR 4 153303070 153303070 single base substitution A C intron_variant SKCA-BR 4 153303898 153303898 insertion of <=200bp - TA intron_variant SKCA-BR 4 153303898 153303898 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 4 153304816 153304816 single base substitution G A intron_variant SKCA-BR 4 153304816 153304816 single base substitution G A upstream_gene_variant SKCA-BR 4 153309167 153309167 single base substitution C A intron_variant SKCA-BR 4 153313971 153313971 single base substitution G A intron_variant SKCA-BR 4 153321194 153321194 single base substitution C T intron_variant SKCA-BR 4 153331458 153331458 single base substitution G A downstream_gene_variant SKCA-BR 4 153331458 153331458 single base substitution G A intron_variant SKCA-BR 4 153333509 153333509 single base substitution G T intron_variant SKCA-BR 4 153333509 153333509 single base substitution G T upstream_gene_variant SKCA-BR 4 153340646 153340646 insertion of <=200bp - AAAAC intron_variant SKCA-BR 4 153340648 153340648 single base substitution C A intron_variant SKCA-BR 4 153340758 153340758 single base substitution C T intron_variant SKCA-BR 4 153347505 153347506 deletion of <=200bp CT - intron_variant SKCA-BR 4 153347605 153347605 single base substitution G A intron_variant SKCA-BR 4 153350313 153350313 single base substitution G T intron_variant SKCA-BR 4 153355649 153355649 single base substitution T C intron_variant SKCA-BR 4 153355929 153355929 single base substitution T C intron_variant SKCA-BR 4 153356305 153356305 single base substitution C T intron_variant SKCA-BR 4 153358095 153358095 single base substitution T C intron_variant SKCA-BR 4 153364018 153364018 single base substitution G A intron_variant SKCA-BR 4 153370029 153370029 single base substitution G A intron_variant SKCA-BR 4 153375761 153375761 single base substitution G A intron_variant SKCA-BR 4 153376095 153376095 single base substitution C T intron_variant SKCA-BR 4 153377856 153377856 single base substitution T A intron_variant SKCA-BR 4 153379401 153379401 single base substitution A C intron_variant SKCA-BR 4 153382961 153382961 single base substitution G A intron_variant SKCA-BR 4 153391261 153391261 single base substitution G A intron_variant SKCA-BR 4 153396059 153396059 single base substitution G T intron_variant SKCA-BR 4 153396701 153396701 single base substitution G A intron_variant SKCA-BR 4 153401893 153401893 single base substitution A C intron_variant SKCA-BR 4 153402923 153402923 single base substitution G A intron_variant SKCA-BR 4 153410079 153410079 single base substitution G A intron_variant SKCA-BR 4 153412738 153412738 single base substitution T G intron_variant SKCA-BR 4 153412743 153412743 single base substitution A G intron_variant SKCA-BR 4 153412765 153412765 single base substitution T G intron_variant SKCA-BR 4 153415946 153415946 single base substitution G A intron_variant SKCA-BR 4 153418473 153418474 deletion of <=200bp CA - intron_variant SKCA-BR 4 153419447 153419447 insertion of <=200bp - CAA intron_variant SKCA-BR 4 153420733 153420733 single base substitution G A intron_variant SKCA-BR 4 153421604 153421604 single base substitution A C intron_variant SKCA-BR 4 153422163 153422163 single base substitution G A intron_variant SKCA-BR 4 153425954 153425954 single base substitution G A intron_variant SKCA-BR 4 153426352 153426352 single base substitution T A intron_variant SKCA-BR 4 153435567 153435567 single base substitution A C intron_variant SKCA-BR 4 153436922 153436922 single base substitution G T intron_variant SKCA-BR 4 153440475 153440475 single base substitution G T intron_variant SKCA-BR 4 153449017 153449017 insertion of <=200bp - TAC downstream_gene_variant SKCA-BR 4 153449017 153449017 insertion of <=200bp - TAC intron_variant SKCA-BR 4 153449017 153449017 insertion of <=200bp - TATAC downstream_gene_variant SKCA-BR 4 153449017 153449017 insertion of <=200bp - TATAC intron_variant SKCA-BR 4 153449319 153449319 single base substitution C G downstream_gene_variant SKCA-BR 4 153449319 153449319 single base substitution C G intron_variant SKCA-BR 4 153450641 153450641 single base substitution A C downstream_gene_variant SKCA-BR 4 153450641 153450641 single base substitution A C intron_variant SKCA-BR 4 153456425 153456425 single base substitution T C 5_prime_UTR_variant SKCA-BR 4 153456425 153456425 single base substitution T C upstream_gene_variant SKCA-BR 4 153457245 153457245 single base substitution A G 5_prime_UTR_variant SKCA-BR 4 153457245 153457245 single base substitution A G upstream_gene_variant SKCA-BR 4 153457409 153457409 single base substitution G A upstream_gene_variant SKCA-BR 4 153457979 153457979 single base substitution C T upstream_gene_variant SKCA-BR 4 153459893 153459893 single base substitution C T upstream_gene_variant SKCA-BR 4 153459894 153459894 single base substitution C T upstream_gene_variant SKCM-US 4 153245389 153245389 single base substitution G A downstream_gene_variant SKCM-US 4 153245389 153245389 single base substitution G A exon_variant SKCM-US 4 153245389 153245389 single base substitution G A missense_variant S425F 1274C>T SKCM-US 4 153245389 153245389 single base substitution G A missense_variant S483F 1448C>T SKCM-US 4 153245389 153245389 single base substitution G A missense_variant S521F 1562C>T SKCM-US 4 153245389 153245389 single base substitution G A missense_variant S601F 1802C>T SKCM-US 4 153247170 153247170 single base substitution G C downstream_gene_variant SKCM-US 4 153247170 153247170 single base substitution G C exon_variant SKCM-US 4 153247170 153247170 single base substitution G C synonymous_variant V368V 1104C>G SKCM-US 4 153247170 153247170 single base substitution G C synonymous_variant V426V 1278C>G SKCM-US 4 153247170 153247170 single base substitution G C synonymous_variant V464V 1392C>G SKCM-US 4 153247170 153247170 single base substitution G C synonymous_variant V544V 1632C>G SKCM-US 4 153247170 153247170 single base substitution G C upstream_gene_variant SKCM-US 4 153247254 153247254 single base substitution A C downstream_gene_variant SKCM-US 4 153247254 153247254 single base substitution A C exon_variant SKCM-US 4 153247254 153247254 single base substitution A C missense_variant S340R 1020T>G SKCM-US 4 153247254 153247254 single base substitution A C missense_variant S398R 1194T>G SKCM-US 4 153247254 153247254 single base substitution A C missense_variant S436R 1308T>G SKCM-US 4 153247254 153247254 single base substitution A C missense_variant S516R 1548T>G SKCM-US 4 153247254 153247254 single base substitution A C upstream_gene_variant SKCM-US 4 153247304 153247304 single base substitution G A downstream_gene_variant SKCM-US 4 153247304 153247304 single base substitution G A exon_variant SKCM-US 4 153247304 153247304 single base substitution G A missense_variant H324Y 970C>T SKCM-US 4 153247304 153247304 single base substitution G A missense_variant H382Y 1144C>T SKCM-US 4 153247304 153247304 single base substitution G A missense_variant H420Y 1258C>T SKCM-US 4 153247304 153247304 single base substitution G A missense_variant H500Y 1498C>T SKCM-US 4 153247304 153247304 single base substitution G A upstream_gene_variant SKCM-US 4 153247366 153247366 single base substitution C T downstream_gene_variant SKCM-US 4 153247366 153247366 single base substitution C T exon_variant SKCM-US 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A SKCM-US 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A SKCM-US 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A SKCM-US 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A SKCM-US 4 153247366 153247366 single base substitution C T upstream_gene_variant SKCM-US 4 153249511 153249511 single base substitution C A exon_variant SKCM-US 4 153249511 153249511 single base substitution C A stop_gained G247* 739G>T SKCM-US 4 153249511 153249511 single base substitution C A stop_gained G305* 913G>T SKCM-US 4 153249511 153249511 single base substitution C A stop_gained G343* 1027G>T SKCM-US 4 153249511 153249511 single base substitution C A stop_gained G423* 1267G>T SKCM-US 4 153249511 153249511 single base substitution C A upstream_gene_variant SKCM-US 4 153251889 153251889 single base substitution G A exon_variant SKCM-US 4 153251889 153251889 single base substitution G A missense_variant P197S 589C>T SKCM-US 4 153251889 153251889 single base substitution G A missense_variant P255S 763C>T SKCM-US 4 153251889 153251889 single base substitution G A missense_variant P293S 877C>T SKCM-US 4 153251889 153251889 single base substitution G A missense_variant P373S 1117C>T SKCM-US 4 153251889 153251889 single base substitution G A upstream_gene_variant SKCM-US 4 153251903 153251903 single base substitution C T exon_variant SKCM-US 4 153251903 153251903 single base substitution C T missense_variant G192E 575G>A SKCM-US 4 153251903 153251903 single base substitution C T missense_variant G250E 749G>A SKCM-US 4 153251903 153251903 single base substitution C T missense_variant G288E 863G>A SKCM-US 4 153251903 153251903 single base substitution C T missense_variant G368E 1103G>A SKCM-US 4 153251903 153251903 single base substitution C T upstream_gene_variant SKCM-US 4 153253840 153253840 single base substitution G A exon_variant SKCM-US 4 153253840 153253840 single base substitution G A missense_variant P122L 365C>T SKCM-US 4 153253840 153253840 single base substitution G A missense_variant P180L 539C>T SKCM-US 4 153253840 153253840 single base substitution G A missense_variant P218L 653C>T SKCM-US 4 153253840 153253840 single base substitution G A missense_variant P298L 893C>T SKCM-US 4 153253840 153253840 single base substitution G A upstream_gene_variant SKCM-US 4 153268087 153268087 single base substitution A G exon_variant SKCM-US 4 153268087 153268087 single base substitution A G missense_variant F123L 367T>C SKCM-US 4 153268087 153268087 single base substitution A G missense_variant F161L 481T>C SKCM-US 4 153268087 153268087 single base substitution A G missense_variant F241L 721T>C SKCM-US 4 153268087 153268087 single base substitution A G missense_variant F65L 193T>C SKCM-US 4 153271233 153271233 single base substitution G A exon_variant SKCM-US 4 153271233 153271233 single base substitution G A missense_variant S102F 305C>T SKCM-US 4 153271233 153271233 single base substitution G A missense_variant S182F 545C>T SKCM-US 4 153271233 153271233 single base substitution G A missense_variant S64F 191C>T SKCM-US 4 153271233 153271233 single base substitution G A upstream_gene_variant SKCM-US 4 153332598 153332598 single base substitution G A stop_gained Q120* 358C>T STAD-US 4 153244115 153244115 insertion of <=200bp - T downstream_gene_variant STAD-US 4 153244115 153244115 insertion of <=200bp - T exon_variant STAD-US 4 153244115 153244115 insertion of <=200bp - T frameshift_variant K505K? STAD-US 4 153244115 153244115 insertion of <=200bp - T frameshift_variant K563K? STAD-US 4 153244115 153244115 insertion of <=200bp - T frameshift_variant K601K? STAD-US 4 153244115 153244115 insertion of <=200bp - T frameshift_variant K681K? STAD-US 4 153244156 153244156 deletion of <=200bp C - downstream_gene_variant STAD-US 4 153244156 153244156 deletion of <=200bp C - exon_variant STAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G491 STAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G549 STAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G587 STAD-US 4 153244156 153244156 deletion of <=200bp C - frameshift_variant G667 STAD-US 4 153244281 153244281 single base substitution C T downstream_gene_variant STAD-US 4 153244281 153244281 single base substitution C T exon_variant STAD-US 4 153244281 153244281 single base substitution C T missense_variant A450T 1348G>A STAD-US 4 153244281 153244281 single base substitution C T missense_variant A508T 1522G>A STAD-US 4 153244281 153244281 single base substitution C T missense_variant A546T 1636G>A STAD-US 4 153244281 153244281 single base substitution C T missense_variant A626T 1876G>A STAD-US 4 153245514 153245514 single base substitution A G downstream_gene_variant STAD-US 4 153245514 153245514 single base substitution A G exon_variant STAD-US 4 153245514 153245514 single base substitution A G synonymous_variant L383L 1149T>C STAD-US 4 153245514 153245514 single base substitution A G synonymous_variant L441L 1323T>C STAD-US 4 153245514 153245514 single base substitution A G synonymous_variant L479L 1437T>C STAD-US 4 153245514 153245514 single base substitution A G synonymous_variant L559L 1677T>C STAD-US 4 153247167 153247167 single base substitution A C downstream_gene_variant STAD-US 4 153247167 153247167 single base substitution A C exon_variant STAD-US 4 153247167 153247167 single base substitution A C stop_gained Y369* 1107T>G STAD-US 4 153247167 153247167 single base substitution A C stop_gained Y427* 1281T>G STAD-US 4 153247167 153247167 single base substitution A C stop_gained Y465* 1395T>G STAD-US 4 153247167 153247167 single base substitution A C stop_gained Y545* 1635T>G STAD-US 4 153247167 153247167 single base substitution A C upstream_gene_variant STAD-US 4 153247289 153247289 single base substitution G A downstream_gene_variant STAD-US 4 153247289 153247289 single base substitution G A exon_variant STAD-US 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T STAD-US 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T STAD-US 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T STAD-US 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T STAD-US 4 153247289 153247289 single base substitution G A upstream_gene_variant STAD-US 4 153247360 153247360 single base substitution G A downstream_gene_variant STAD-US 4 153247360 153247360 single base substitution G A exon_variant STAD-US 4 153247360 153247360 single base substitution G A missense_variant A305V 914C>T STAD-US 4 153247360 153247360 single base substitution G A missense_variant A363V 1088C>T STAD-US 4 153247360 153247360 single base substitution G A missense_variant A401V 1202C>T STAD-US 4 153247360 153247360 single base substitution G A missense_variant A481V 1442C>T STAD-US 4 153247360 153247360 single base substitution G A upstream_gene_variant STAD-US 4 153247366 153247366 single base substitution C T downstream_gene_variant STAD-US 4 153247366 153247366 single base substitution C T exon_variant STAD-US 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A STAD-US 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A STAD-US 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A STAD-US 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A STAD-US 4 153247366 153247366 single base substitution C T upstream_gene_variant STAD-US 4 153249361 153249361 deletion of <=200bp T - frameshift_variant R297 STAD-US 4 153249361 153249361 deletion of <=200bp T - frameshift_variant R355 STAD-US 4 153249361 153249361 deletion of <=200bp T - frameshift_variant R393 STAD-US 4 153249361 153249361 deletion of <=200bp T - frameshift_variant R473 STAD-US 4 153249361 153249361 deletion of <=200bp T - splice_region_variant STAD-US 4 153249361 153249361 deletion of <=200bp T - upstream_gene_variant STAD-US 4 153249361 153249361 insertion of <=200bp - T frameshift_variant R297K? STAD-US 4 153249361 153249361 insertion of <=200bp - T frameshift_variant R355K? STAD-US 4 153249361 153249361 insertion of <=200bp - T frameshift_variant R393K? STAD-US 4 153249361 153249361 insertion of <=200bp - T frameshift_variant R473K? STAD-US 4 153249361 153249361 insertion of <=200bp - T splice_region_variant STAD-US 4 153249361 153249361 insertion of <=200bp - T upstream_gene_variant STAD-US 4 153249384 153249384 single base substitution C T exon_variant STAD-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A STAD-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A STAD-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A STAD-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A STAD-US 4 153249384 153249384 single base substitution C T upstream_gene_variant STAD-US 4 153249385 153249385 single base substitution G A exon_variant STAD-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T STAD-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T STAD-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T STAD-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T STAD-US 4 153249385 153249385 single base substitution G A upstream_gene_variant STAD-US 4 153250850 153250850 single base substitution T C exon_variant STAD-US 4 153250850 153250850 single base substitution T C missense_variant K228E 682A>G STAD-US 4 153250850 153250850 single base substitution T C missense_variant K286E 856A>G STAD-US 4 153250850 153250850 single base substitution T C missense_variant K324E 970A>G STAD-US 4 153250850 153250850 single base substitution T C missense_variant K404E 1210A>G STAD-US 4 153250850 153250850 single base substitution T C upstream_gene_variant STAD-US 4 153251934 153251934 single base substitution G A exon_variant STAD-US 4 153251934 153251934 single base substitution G A stop_gained Q182* 544C>T STAD-US 4 153251934 153251934 single base substitution G A stop_gained Q240* 718C>T STAD-US 4 153251934 153251934 single base substitution G A stop_gained Q278* 832C>T STAD-US 4 153251934 153251934 single base substitution G A stop_gained Q358* 1072C>T STAD-US 4 153251934 153251934 single base substitution G A upstream_gene_variant STAD-US 4 153258955 153258955 single base substitution T A missense_variant E111V 332A>T STAD-US 4 153258955 153258955 single base substitution T A missense_variant E169V 506A>T STAD-US 4 153258955 153258955 single base substitution T A missense_variant E207V 620A>T STAD-US 4 153258955 153258955 single base substitution T A missense_variant E287V 860A>T STAD-US 4 153258983 153258983 single base substitution G A stop_gained R102* 304C>T STAD-US 4 153258983 153258983 single base substitution G A stop_gained R160* 478C>T STAD-US 4 153258983 153258983 single base substitution G A stop_gained R198* 592C>T STAD-US 4 153258983 153258983 single base substitution G A stop_gained R278* 832C>T STAD-US 4 153268090 153268090 deletion of <=200bp T - exon_variant STAD-US 4 153268090 153268090 deletion of <=200bp T - frameshift_variant M122 STAD-US 4 153268090 153268090 deletion of <=200bp T - frameshift_variant M160 STAD-US 4 153268090 153268090 deletion of <=200bp T - frameshift_variant M240 STAD-US 4 153268090 153268090 deletion of <=200bp T - frameshift_variant M64 STAD-US 4 153271192 153271192 single base substitution A G splice_donor_variant STAD-US 4 153271192 153271192 single base substitution A G upstream_gene_variant STAD-US 4 153332714 153332714 single base substitution T C missense_variant N81S 242A>G STAD-US 4 153332915 153332915 single base substitution C T missense_variant R14Q 41G>A THCA-SA 4 153456102 153456102 single base substitution A G 5_prime_UTR_variant THCA-SA 4 153456102 153456102 single base substitution A G exon_variant UCEC-US 4 153244091 153244091 single base substitution C T downstream_gene_variant UCEC-US 4 153244091 153244091 single base substitution C T exon_variant UCEC-US 4 153244091 153244091 single base substitution C T missense_variant R513Q 1538G>A UCEC-US 4 153244091 153244091 single base substitution C T missense_variant R571Q 1712G>A UCEC-US 4 153244091 153244091 single base substitution C T missense_variant R609Q 1826G>A UCEC-US 4 153244091 153244091 single base substitution C T missense_variant R689Q 2066G>A UCEC-US 4 153244092 153244092 single base substitution G A downstream_gene_variant UCEC-US 4 153244092 153244092 single base substitution G A exon_variant UCEC-US 4 153244092 153244092 single base substitution G A missense_variant R513W 1537C>T UCEC-US 4 153244092 153244092 single base substitution G A missense_variant R571W 1711C>T UCEC-US 4 153244092 153244092 single base substitution G A missense_variant R609W 1825C>T UCEC-US 4 153244092 153244092 single base substitution G A missense_variant R689W 2065C>T UCEC-US 4 153244184 153244184 single base substitution C T downstream_gene_variant UCEC-US 4 153244184 153244184 single base substitution C T exon_variant UCEC-US 4 153244184 153244184 single base substitution C T missense_variant R482Q 1445G>A UCEC-US 4 153244184 153244184 single base substitution C T missense_variant R540Q 1619G>A UCEC-US 4 153244184 153244184 single base substitution C T missense_variant R578Q 1733G>A UCEC-US 4 153244184 153244184 single base substitution C T missense_variant R658Q 1973G>A UCEC-US 4 153244185 153244185 single base substitution G A downstream_gene_variant UCEC-US 4 153244185 153244185 single base substitution G A exon_variant UCEC-US 4 153244185 153244185 single base substitution G A stop_gained R482* 1444C>T UCEC-US 4 153244185 153244185 single base substitution G A stop_gained R540* 1618C>T UCEC-US 4 153244185 153244185 single base substitution G A stop_gained R578* 1732C>T UCEC-US 4 153244185 153244185 single base substitution G A stop_gained R658* 1972C>T UCEC-US 4 153247168 153247168 single base substitution T C downstream_gene_variant UCEC-US 4 153247168 153247168 single base substitution T C exon_variant UCEC-US 4 153247168 153247168 single base substitution T C missense_variant Y369C 1106A>G UCEC-US 4 153247168 153247168 single base substitution T C missense_variant Y427C 1280A>G UCEC-US 4 153247168 153247168 single base substitution T C missense_variant Y465C 1394A>G UCEC-US 4 153247168 153247168 single base substitution T C missense_variant Y545C 1634A>G UCEC-US 4 153247168 153247168 single base substitution T C upstream_gene_variant UCEC-US 4 153247289 153247289 single base substitution G A downstream_gene_variant UCEC-US 4 153247289 153247289 single base substitution G A exon_variant UCEC-US 4 153247289 153247289 single base substitution G A missense_variant R329C 985C>T UCEC-US 4 153247289 153247289 single base substitution G A missense_variant R387C 1159C>T UCEC-US 4 153247289 153247289 single base substitution G A missense_variant R425C 1273C>T UCEC-US 4 153247289 153247289 single base substitution G A missense_variant R505C 1513C>T UCEC-US 4 153247289 153247289 single base substitution G A upstream_gene_variant UCEC-US 4 153247289 153247289 single base substitution G C downstream_gene_variant UCEC-US 4 153247289 153247289 single base substitution G C exon_variant UCEC-US 4 153247289 153247289 single base substitution G C missense_variant R329G 985C>G UCEC-US 4 153247289 153247289 single base substitution G C missense_variant R387G 1159C>G UCEC-US 4 153247289 153247289 single base substitution G C missense_variant R425G 1273C>G UCEC-US 4 153247289 153247289 single base substitution G C missense_variant R505G 1513C>G UCEC-US 4 153247289 153247289 single base substitution G C upstream_gene_variant UCEC-US 4 153247366 153247366 single base substitution C T downstream_gene_variant UCEC-US 4 153247366 153247366 single base substitution C T exon_variant UCEC-US 4 153247366 153247366 single base substitution C T missense_variant R303Q 908G>A UCEC-US 4 153247366 153247366 single base substitution C T missense_variant R361Q 1082G>A UCEC-US 4 153247366 153247366 single base substitution C T missense_variant R399Q 1196G>A UCEC-US 4 153247366 153247366 single base substitution C T missense_variant R479Q 1436G>A UCEC-US 4 153247366 153247366 single base substitution C T upstream_gene_variant UCEC-US 4 153249384 153249384 single base substitution C T exon_variant UCEC-US 4 153249384 153249384 single base substitution C T missense_variant R289H 866G>A UCEC-US 4 153249384 153249384 single base substitution C T missense_variant R347H 1040G>A UCEC-US 4 153249384 153249384 single base substitution C T missense_variant R385H 1154G>A UCEC-US 4 153249384 153249384 single base substitution C T missense_variant R465H 1394G>A UCEC-US 4 153249384 153249384 single base substitution C T upstream_gene_variant UCEC-US 4 153249385 153249385 single base substitution G A exon_variant UCEC-US 4 153249385 153249385 single base substitution G A missense_variant R289C 865C>T UCEC-US 4 153249385 153249385 single base substitution G A missense_variant R347C 1039C>T UCEC-US 4 153249385 153249385 single base substitution G A missense_variant R385C 1153C>T UCEC-US 4 153249385 153249385 single base substitution G A missense_variant R465C 1393C>T UCEC-US 4 153249385 153249385 single base substitution G A upstream_gene_variant UCEC-US 4 153249456 153249456 single base substitution C T exon_variant UCEC-US 4 153249456 153249456 single base substitution C T missense_variant R265Q 794G>A UCEC-US 4 153249456 153249456 single base substitution C T missense_variant R323Q 968G>A UCEC-US 4 153249456 153249456 single base substitution C T missense_variant R361Q 1082G>A UCEC-US 4 153249456 153249456 single base substitution C T missense_variant R441Q 1322G>A UCEC-US 4 153249456 153249456 single base substitution C T upstream_gene_variant UCEC-US 4 153249510 153249510 single base substitution C A exon_variant UCEC-US 4 153249510 153249510 single base substitution C A missense_variant G247V 740G>T UCEC-US 4 153249510 153249510 single base substitution C A missense_variant G305V 914G>T UCEC-US 4 153249510 153249510 single base substitution C A missense_variant G343V 1028G>T UCEC-US 4 153249510 153249510 single base substitution C A missense_variant G423V 1268G>T UCEC-US 4 153249510 153249510 single base substitution C A upstream_gene_variant UCEC-US 4 153249526 153249526 single base substitution C T exon_variant UCEC-US 4 153249526 153249526 single base substitution C T missense_variant V242M 724G>A UCEC-US 4 153249526 153249526 single base substitution C T missense_variant V300M 898G>A UCEC-US 4 153249526 153249526 single base substitution C T missense_variant V338M 1012G>A UCEC-US 4 153249526 153249526 single base substitution C T missense_variant V418M 1252G>A UCEC-US 4 153249526 153249526 single base substitution C T upstream_gene_variant UCEC-US 4 153250883 153250883 single base substitution G A exon_variant UCEC-US 4 153250883 153250883 single base substitution G A stop_gained R217* 649C>T UCEC-US 4 153250883 153250883 single base substitution G A stop_gained R275* 823C>T UCEC-US 4 153250883 153250883 single base substitution G A stop_gained R313* 937C>T UCEC-US 4 153250883 153250883 single base substitution G A stop_gained R393* 1177C>T UCEC-US 4 153250883 153250883 single base substitution G A upstream_gene_variant UCEC-US 4 153250916 153250916 single base substitution G T exon_variant UCEC-US 4 153250916 153250916 single base substitution G T missense_variant H206N 616C>A UCEC-US 4 153250916 153250916 single base substitution G T missense_variant H264N 790C>A UCEC-US 4 153250916 153250916 single base substitution G T missense_variant H302N 904C>A UCEC-US 4 153250916 153250916 single base substitution G T missense_variant H382N 1144C>A UCEC-US 4 153250916 153250916 single base substitution G T upstream_gene_variant UCEC-US 4 153251901 153251901 single base substitution C A exon_variant UCEC-US 4 153251901 153251901 single base substitution C A stop_gained E193* 577G>T UCEC-US 4 153251901 153251901 single base substitution C A stop_gained E251* 751G>T UCEC-US 4 153251901 153251901 single base substitution C A stop_gained E289* 865G>T UCEC-US 4 153251901 153251901 single base substitution C A stop_gained E369* 1105G>T UCEC-US 4 153251901 153251901 single base substitution C A upstream_gene_variant UCEC-US 4 153253747 153253747 deletion of <=200bp C - splice_donor_variant UCEC-US 4 153253747 153253747 deletion of <=200bp C - upstream_gene_variant UCEC-US 4 153253775 153253775 single base substitution G T exon_variant UCEC-US 4 153253775 153253775 single base substitution G T missense_variant L144I 430C>A UCEC-US 4 153253775 153253775 single base substitution G T missense_variant L202I 604C>A UCEC-US 4 153253775 153253775 single base substitution G T missense_variant L240I 718C>A UCEC-US 4 153253775 153253775 single base substitution G T missense_variant L320I 958C>A UCEC-US 4 153253775 153253775 single base substitution G T upstream_gene_variant UCEC-US 4 153259012 153259013 deletion of <=200bp AT - frameshift_variant M150 UCEC-US 4 153259012 153259013 deletion of <=200bp AT - frameshift_variant M188 UCEC-US 4 153259012 153259013 deletion of <=200bp AT - frameshift_variant M268 UCEC-US 4 153259012 153259013 deletion of <=200bp AT - frameshift_variant M92 UCEC-US 4 153259071 153259071 single base substitution C A missense_variant E130D 390G>T UCEC-US 4 153259071 153259071 single base substitution C A missense_variant E168D 504G>T UCEC-US 4 153259071 153259071 single base substitution C A missense_variant E248D 744G>T UCEC-US 4 153259071 153259071 single base substitution C A missense_variant E72D 216G>T UCEC-US 4 153259076 153259076 single base substitution G T missense_variant P129T 385C>A UCEC-US 4 153259076 153259076 single base substitution G T missense_variant P167T 499C>A UCEC-US 4 153259076 153259076 single base substitution G T missense_variant P247T 739C>A UCEC-US 4 153259076 153259076 single base substitution G T missense_variant P71T 211C>A UCEC-US 4 153268097 153268097 single base substitution C T exon_variant UCEC-US 4 153268097 153268097 single base substitution C T stop_gained W119* 357G>A UCEC-US 4 153268097 153268097 single base substitution C T stop_gained W157* 471G>A UCEC-US 4 153268097 153268097 single base substitution C T stop_gained W237* 711G>A UCEC-US 4 153268097 153268097 single base substitution C T stop_gained W61* 183G>A UCEC-US 4 153268137 153268137 single base substitution C T exon_variant UCEC-US 4 153268137 153268137 single base substitution C T missense_variant R106Q 317G>A UCEC-US 4 153268137 153268137 single base substitution C T missense_variant R144Q 431G>A UCEC-US 4 153268137 153268137 single base substitution C T missense_variant R224Q 671G>A UCEC-US 4 153268137 153268137 single base substitution C T missense_variant R48Q 143G>A UCEC-US 4 153268138 153268138 single base substitution G A exon_variant UCEC-US 4 153268138 153268138 single base substitution G A stop_gained R106* 316C>T UCEC-US 4 153268138 153268138 single base substitution G A stop_gained R144* 430C>T UCEC-US 4 153268138 153268138 single base substitution G A stop_gained R224* 670C>T UCEC-US 4 153268138 153268138 single base substitution G A stop_gained R48* 142C>T UCEC-US 4 153273708 153273708 single base substitution G A exon_variant UCEC-US 4 153273708 153273708 single base substitution G A intron_variant UCEC-US 4 153273708 153273708 single base substitution G A missense_variant R59W 175C>T UCEC-US 4 153273708 153273708 single base substitution G A upstream_gene_variant UCEC-US 4 153303342 153303342 single base substitution C T intron_variant UCEC-US 4 153303342 153303342 single base substitution C T missense_variant R49Q 146G>A UCEC-US 4 153332524 153332524 single base substitution C T synonymous_variant T144T 432G>A UCEC-US 4 153332553 153332553 single base substitution C A missense_variant D135Y 403G>T UCEC-US 4 153332570 153332570 single base substitution T G missense_variant D129A 386A>C UCEC-US 4 153332802 153332802 single base substitution G A missense_variant H52Y 154C>T UCEC-US 4 153332916 153332916 single base substitution G A stop_gained R14* 40C>T UCEC-US 4 153332919 153332919 single base substitution G A stop_gained R13* 37C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AP-A05P-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - sysucc-274T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 12829/93C COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - B89-10-Tumor COSM1753578 c.1311A>T p.G437G Substitution - coding silent 4:152328315-152328315 - TCGA-AG-3742-01 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - HSB2 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2379663 COSM5031087 c.? p.? Unknown TCGA-AD-6889-01 COSM1427915 c.277G>T p.G93* Substitution - Nonsense 4:152411527-152411527 - PD9571a COSM5752726 c.145G>T p.E49* Substitution - Nonsense 4:152411659-152411659 - 2138878 COSM3718360 c.? p.W244* Substitution - Nonsense 1118427 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - pfg054T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 195 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1813474 COSM33843 c.? p.R465C Substitution - Missense 2541163 COSM28490 c.? p.? Unknown 1219461 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - 1244707 COSM33978 c.861_862ins49 p.L288fs*45 Insertion - Frameshift CP66-MEL COSM22388 c.328G>T p.E110* Substitution - Nonsense 4:152411476-152411476 - TCGA-AA-3833-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - DLBCL922 COSM1580892 c.302A>T p.D101V Substitution - Missense 4:152411502-152411502 - 85T COSM302215 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - 2492722 COSM5723743 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - TCGA-C4-A0F0-01 COSM420162 c.963G>A p.W321* Substitution - Nonsense 4:152332618-152332618 - TCGA-C5-A1BJ-01 COSM420170 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - 587254 COSM1206879 c.664C>T p.R222* Substitution - Nonsense 4:152346992-152346992 - PCSI_0090_Pa_P COSM3380836 c.778T>C p.C260R Substitution - Missense 4:152337885-152337885 - SW837 COSM3128010 c.1208_1209insT p.L403fs*34 Insertion - Frameshift 4:152329699-152329700 - 587260 COSM1206882 c.770T>A p.I257N Substitution - Missense 4:152337893-152337893 - P6 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ESCC-F18 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AX-A05S-01 COSM22989 c.1634A>G p.Y545C Substitution - Missense 4:152326016-152326016 - RMS2111 COSM5677867 c.1321C>G p.R441G Substitution - Missense 4:152328305-152328305 - 1247748 COSM33843 c.? p.R465C Substitution - Missense 3940 COSM5751205 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - SM4 COSM87015 c.? p.R278* Substitution - Nonsense 2379664 COSM5031087 c.? p.? Unknown 2379660 COSM5031087 c.? p.? Unknown TL42 COSM5751819 c.1034G>GT p.I347fs*16 Complex - frameshift 4:152330820-152330820 - TCGA-CA-6717-01 COSM1427802 c.1178G>A p.R393Q Substitution - Missense 4:152329730-152329730 - TCGA-JW-A5VJ-01 COSM4818414 c.1522C>T p.Q508* Substitution - Nonsense 4:152326128-152326128 - CLL042 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1813487 COSM33842 c.? p.R465H Substitution - Missense 1677150 COSM33842 c.? p.R465H Substitution - Missense sysucc-834T COSM5486405 c.1852C>T p.Q618* Substitution - Nonsense 4:152324187-152324187 - 2467872 COSM5031087 c.? p.? Unknown HN_00338 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-E9-A22E-01 COSM1485737 c.1172G>A p.G391D Substitution - Missense 4:152329736-152329736 - TCGA-Q1-A73O-01 COSM206685 c.1973G>A p.R658Q Substitution - Missense 4:152323032-152323032 - ESCC-205T COSM3940767 c.1310G>A p.G437E Substitution - Missense 4:152328316-152328316 - 1115498 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D1-A103-01 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-EE-A2A2-06 COSM3600946 c.358C>T p.Q120* Substitution - Nonsense 4:152411446-152411446 - CEM COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 587400 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - ESCC_130 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - 01-P8014 COSM4584837 c.321A>G p.E107E Substitution - coding silent 4:152411483-152411483 - 2471684 COSM33842 c.? p.R465H Substitution - Missense 2138884 COSM3718364 c.? p.G499fs*25 Unknown T3094 COSM4684118 c.1381A>G p.T461A Substitution - Missense 4:152328245-152328245 - ccRCC-64 COSM1659853 c.1636T>C p.S546P Substitution - Missense 4:152326014-152326014 - T69 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - LUAD-LIP77 COSM342476 c.631G>A p.D211N Substitution - Missense 4:152347025-152347025 - TCGA-AK-3447-01 COSM1495747 c.486T>A p.Y162* Substitution - Nonsense 4:152411318-152411318 - CSCC-38-T COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - TCGA-CL-5918-01 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1044489 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - B-ALL2 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1N22-VS-1T22 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-CM-4750-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-AP-A051-01 COSM1052099 c.1252G>A p.V418M Substitution - Missense 4:152328374-152328374 - Gp5D COSM3127941 c.1739A>G p.H580R Substitution - Missense 4:152324300-152324300 - 2471672 COSM33842 c.? p.R465H Substitution - Missense SJTALL190 COSM4603681 c.?_?ins10 p.R393fs*? Insertion - Frameshift 16 COSM5731180 c.1468A>G p.T490A Substitution - Missense 4:152326182-152326182 - TCGA-DI-A1NN-01 COSM1052139 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - 1556290 COSM133117 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - ESCC-F34 COSM3767733 c.1438G>A p.D480N Substitution - Missense 4:152326212-152326212 - T3499 COSM4684108 c.1738C>G p.H580D Substitution - Missense 4:152324301-152324301 - TCGA-EA-A50E-01 COSM420162 c.963G>A p.W321* Substitution - Nonsense 4:152332618-152332618 - ESCC-F114 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - I2L-P7-Tumor-Organoid COSM5356234 c.726+2T>C p.? Unknown 4:152346928-152346928 - 9583_CLM COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-AA-A01K-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-D1-A16Y-01 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - I2L-P7-Tumor-Organoid COSM5356233 c.726+2T>C p.? Unknown 4:152346928-152346928 - 1813500 COSM1155762 c.? p.R505H Substitution - Missense JURKAT COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-33-4583-01 COSM732391 c.1959G>C p.T653T Substitution - coding silent 4:152323046-152323046 - CSCC-38-T COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - TCGA-G2-A2ES-01 COSM1309813 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - 4760_CLM COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 4132_T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-ER-A19F-06 COSM3600936 c.721T>C p.F241L Substitution - Missense 4:152346935-152346935 - 1115496 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10593/90C COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2492711 COSM5606546 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - WM3702 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - 1118425 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-BL-A13I-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - HN_62376 COSM123130 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - LUAD-F00057 COSM339469 c.328G>T p.E110* Substitution - Nonsense 4:152411476-152411476 - TL42 COSM5751820 c.1034G>GT p.I347fs*16 Complex - frameshift 4:152330820-152330820 - RMS222 COSM5881198 c.1574T>C p.V525A Substitution - Missense 4:152326076-152326076 - 1813489 COSM33842 c.? p.R465H Substitution - Missense 1500574 COSM87018 c.? p.M269I Substitution - Missense 2432698 COSM28490 c.? p.? Unknown TCGA-BH-A2L8-01 COSM3825362 c.1195G>C p.D399H Substitution - Missense 4:152329713-152329713 - TCGA-BS-A0UA-01 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-DS-A0VN-01 COSM460672 c.1557T>A p.Y519* Substitution - Nonsense 4:152326093-152326093 - 1N22-VS-1T22 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - CHC301T COSM3669249 c.1102G>C p.G368R Substitution - Missense 4:152330752-152330752 - 2083400 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HCT15 COSM3128050 c.702C>A p.L234L Substitution - coding silent 4:152346954-152346954 - SNU-C2B COSM3127946 c.1735G>T p.G579W Substitution - Missense 4:152324304-152324304 - ESCC_124 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - MM04T COSM5415240 c.400G>T p.E134* Substitution - Nonsense 4:152411404-152411404 - 1813484 COSM33842 c.? p.R465H Substitution - Missense TCGA-CM-4750-01 COSM5157013 c.109_115delGTAGAGG p.V37fs*24 Deletion - Frameshift 4:152411689-152411695 - sysucc-880T COSM5463320 c.587C>T p.T196I Substitution - Missense 4:152347069-152347069 - Gp2D COSM3127940 c.1739A>G p.H580R Substitution - Missense 4:152324300-152324300 - DM45 COSM5611284 c.180_181TG>GT p.G61* Substitution - Nonsense 4:152411623-152411624 - T1772 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10234 COSM5751237 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - 1043457 COSM22969 c.1398_1399insT p.M467fs*5 Insertion - Frameshift 4:152328227-152328228 - SW48 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - 1115222 COSM27055 c.1510G>A p.V504I Substitution - Missense 4:152326140-152326140 - 435 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - 1556210 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - Relapse_T-ALL16 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AA-A01Z-01 COSM30598 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - TCGA-AP-A056-01 COSM1052137 c.671G>A p.R224Q Substitution - Missense 4:152346985-152346985 - TBR05 COSM4168006 c.1310G>T p.G437V Substitution - Missense 4:152328316-152328316 - 16 COSM5731179 c.1468A>G p.T490A Substitution - Missense 4:152326182-152326182 - TCGA-AA-A01K-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T47 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2157519 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AA-3681-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - CCRF-CEM COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-C4-A0F1-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-18-5595-01 COSM33763 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 3N57-VS-3T57 COSM4984007 c.763G>T p.E255* Substitution - Nonsense 4:152337900-152337900 - 1813479 COSM33843 c.? p.R465C Substitution - Missense B106-Tumor COSM1753571 c.1590T>G p.T530T Substitution - coding silent 4:152326060-152326060 - 2138886 COSM3718361 c.? p.R222* Substitution - Nonsense SW1463 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - Region-27 COSM5748990 c.598G>T p.V200L Substitution - Missense 4:152347058-152347058 - 127T COSM302215 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - S02243 COSM5677866 c.1321C>G p.R441G Substitution - Missense 4:152328305-152328305 - TCGA-D1-A17Q-01 COSM1052134 c.711G>A p.W237* Substitution - Nonsense 4:152346945-152346945 - TCGA-B5-A0JY-01 COSM1052106 c.1144C>A p.H382N Substitution - Missense 4:152329764-152329764 - 1738970 COSM27052 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - 09-128 COSM1645483 c.1667G>A p.S556N Substitution - Missense 4:152324372-152324372 - TCGA-22-4604-01 COSM732383 c.1550G>A p.G517E Substitution - Missense 4:152326100-152326100 - TCGA-04-1337-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T-LBL-64 COSM33844 c.? p.R505C Substitution - Missense 1044509 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - U266-1984 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T1184 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-A8-A0A6-01 COSM3825357 c.1537A>G p.R513G Substitution - Missense 4:152326113-152326113 - 2718 COSM5751152 c.1268G>GT p.V424fs*13 Complex - frameshift 4:152328358-152328358 - 1953_T COSM3946066 c.127C>A p.Q43K Substitution - Missense 4:152411677-152411677 - 185T COSM4381109 c.726+2delT p.? Unknown 4:152346928-152346928 - TCGA-AX-A1C7-01 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 2321345 COSM673925 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - E9 COSM1666338 c.1112A>C p.K371T Substitution - Missense 4:152330742-152330742 - TCGA-DS-A1OA-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 8016470 COSM1427802 c.1178G>A p.R393Q Substitution - Missense 4:152329730-152329730 - 1116947 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 4084 COSM5751237 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - 15935/93M COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - DLBCL737 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - YUWHIM COSM1695080 c.1499A>G p.H500R Substitution - Missense 4:152326151-152326151 - TCGA-GM-A2D9-01 COSM3825367 c.1011G>A p.K337K Substitution - coding silent 4:152330843-152330843 - TCGA-D5-6531-01 COSM5163240 c.1161_1162insA p.Q388fs*5 Insertion - Frameshift 4:152329746-152329747 - 2471686 COSM33842 c.? p.R465H Substitution - Missense 1813492 COSM1155757 c.? p.R473G Substitution - Missense B89-10 COSM1753578 c.1311A>T p.G437G Substitution - coding silent 4:152328315-152328315 - 1738933 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - CLL012 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD24208a COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD4106a COSM161030 c.244A>T p.N82Y Substitution - Missense 4:152411560-152411560 - 2321302 COSM4774925 c.1393C>A p.R465S Substitution - Missense 4:152328233-152328233 - DM26 COSM5608733 c.703C>T p.Q235* Substitution - Nonsense 4:152346953-152346953 - 166 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - CRC-19T COSM5481865 c.833G>A p.R278Q Substitution - Missense 4:152337830-152337830 - 1115201 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AA-3831-01 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - T69 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-BK-A0C9-01 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - PD6086a COSM4383976 c.1859C>T p.P620L Substitution - Missense 4:152323146-152323146 - HPB_ALL COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-22-4604-01 COSM732384 c.1550G>A p.G517E Substitution - Missense 4:152326100-152326100 - TCGA-BR-8380-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-FU-A5XV-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - CLL042 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - D6 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-AP-A056-01 COSM1052109 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - TL28 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - KER COSM33845 c.? p.R479Q Substitution - Missense 1677147 COSM33843 c.? p.R465C Substitution - Missense PD6266a COSM4385612 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - P13 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1994256 COSM1666666 c.1642C>T p.Q548* Substitution - Nonsense 4:152326008-152326008 - TCGA-E9-A22E-01 COSM1485738 c.1172G>A p.G391D Substitution - Missense 4:152329736-152329736 - 2379665 COSM5031087 c.? p.? Unknown 2492721 COSM5723744 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - C113 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-HU-A4GN-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - STC246 COSM1052091 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - TCGA-BS-A0UA-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D9-A1JW-06 COSM3917249 c.1548T>G p.S516R Substitution - Missense 4:152326102-152326102 - 1N47-VS-1T47 COSM4976334 c.1090_1093delAACT p.N364fs*12 Deletion - Frameshift 4:152330761-152330764 - Pa34X COSM84874 c.1688T>C p.I563T Substitution - Missense 4:152324351-152324351 - 1219466 COSM30597 c.892C>T p.P298S Substitution - Missense 4:152332689-152332689 - 1813495 COSM1155768 c.? p.? Unknown 4:152328207-152328207 - TCGA-AM-5820-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - J-RT3-T3-5 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD2720a COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - LC163 COSM5369828 c.1519G>A p.V507I Substitution - Missense 4:152326131-152326131 - 1813483 COSM33842 c.? p.R465H Substitution - Missense T-LBL-2 COSM5885260 c.? p.*708fs*54 Frameshift TCGA-EI-6917-01 COSM1427865 c.845C>A p.S282* Substitution - Nonsense 4:152337818-152337818 - ESCC_118 COSM5640306 c.1922C>G p.S641* Substitution - Nonsense 4:152323083-152323083 - C32 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-60-2722-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-BR-4371-01 COSM4122759 c.1635T>G p.Y545* Substitution - Nonsense 4:152326015-152326015 - TCGA-GF-A3OT-06 COSM3600946 c.358C>T p.Q120* Substitution - Nonsense 4:152411446-152411446 - CLL035 COSM1291848 c.840C>A p.F280L Substitution - Missense 4:152337823-152337823 - S02249 COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - BE-13 COSM27062 c.?_?del? p.? Unknown 1206694 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1044504 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - DLBCL834 COSM206717 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - SW837 COSM3128009 c.1208_1209insT p.L403fs*34 Insertion - Frameshift 4:152329699-152329700 - 587234 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - P12-ISHIKAWA COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1499692 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T1772 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CSCC-62-T COSM4448894 c.1419-2A>C p.? Unknown 4:152326233-152326233 - 1813473 COSM33843 c.? p.R465C Substitution - Missense TCGA-A8-A09M-01 COSM447501 c.902T>C p.L301P Substitution - Missense 4:152332679-152332679 - BD114T COSM5502911 c.1320delT p.R441fs*57 Deletion - Frameshift 4:152328306-152328306 - TCGA-D1-A17Q-01 COSM281109 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - 1556248 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-CD-A4MJ-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CLL035 COSM1291849 c.840C>A p.F280L Substitution - Missense 4:152337823-152337823 - BD205T COSM5490552 c.1693G>T p.V565F Substitution - Missense 4:152324346-152324346 - HCT15 COSM3128049 c.702C>A p.L234L Substitution - coding silent 4:152346954-152346954 - 587322 COSM1206898 c.1679A>G p.D560G Substitution - Missense 4:152324360-152324360 - 3822/93M COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - TCGA-D1-A15X-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-E2-A574-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AA-3833-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 4760_CLM COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-BR-8680-01 COSM206732 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 2541159 COSM28490 c.? p.? Unknown TCGA-EW-A1PE-01 COSM1485743 c.1070G>A p.R357K Substitution - Missense 4:152330784-152330784 - TCGA-Q1-A73O-01 COSM206687 c.1973G>A p.R658Q Substitution - Missense 4:152323032-152323032 - 2379658 COSM5031087 c.? p.? Unknown TCGA-D1-A101-01 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 1874642 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 804-02-4TD COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - WM39 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - TCGA-CG-5721-01 COSM4122764 c.1442C>T p.A481V Substitution - Missense 4:152326208-152326208 - ICGC_MB78 COSM3765119 c.1834C>T p.Q612* Substitution - Nonsense 4:152324205-152324205 - TL45 COSM5751892 c.2065_2066insA p.R689fs*5 Insertion - Frameshift 4:152322939-152322940 - TCGA-B5-A11N-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - Hx190 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - ESCC_11 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - RK150_C01 COSM3767733 c.1438G>A p.D480N Substitution - Missense 4:152326212-152326212 - T3082 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - SJTALL200 COSM4603682 c.1123G>A p.V375M Substitution - Missense 4:152329785-152329785 - TCGA-AP-A05P-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 13103/93P COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - DM10 COSM5608728 c.925C>A p.R309S Substitution - Missense 4:152332656-152332656 - MM15T COSM5415241 c.1136A>C p.H379P Substitution - Missense 4:152329772-152329772 - CRC-19T COSM5481866 c.833G>A p.R278Q Substitution - Missense 4:152337830-152337830 - CSCC-38-T COSM4534714 c.2113G>A p.D705N Substitution - Missense 4:152322892-152322892 - TCGA-AP-A05A-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 6604 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-CD-A4MJ-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CSCC-17-T COSM4510947 c.852C>T p.L284L Substitution - coding silent 4:152337811-152337811 - 10246 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1813493 COSM1155766 c.? p.R473fs*1 Deletion - Frameshift PD11379a COSM5752536 c.724C>T p.Q242* Substitution - Nonsense 4:152346932-152346932 - 587226 COSM1206888 c.1409A>G p.H470R Substitution - Missense 4:152328217-152328217 - DM26 COSM5608732 c.703C>T p.Q235* Substitution - Nonsense 4:152346953-152346953 - 09-128 COSM1645482 c.1667G>A p.S556N Substitution - Missense 4:152324372-152324372 - ESO-327 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - PD4845a COSM5781538 c.830A>C p.Q277P Substitution - Missense 4:152337833-152337833 - TCGA-AX-A05S-01 COSM1052084 c.1634A>G p.Y545C Substitution - Missense 4:152326016-152326016 - 1206653 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - sysucc-809T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 609 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-BR-A4QL-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ME009T COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1813476 COSM33843 c.? p.R465C Substitution - Missense 11490 COSM5751561 c.1014_1018delAAGAA p.R339fs*22 Deletion - Frameshift 4:152330836-152330840 - S10-24679-TP COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - T3033 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD4100a COSM161028 c.254T>G p.I85S Substitution - Missense 4:152411550-152411550 - 1044495 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - DU-528 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 09-664 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1219470 COSM30599 c.1576T>C p.W526R Substitution - Missense 4:152326074-152326074 - 1043434 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - ESO156PT COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-D1-A17A-01 COSM1052143 c.415C>A p.H139N Substitution - Missense 4:152411389-152411389 - SC_9008 COSM1309807 c.1637C>T p.S546L Substitution - Missense 4:152326013-152326013 - 4084 COSM5751243 c.121C>CT p.Q41fs*18 Complex - frameshift 4:152411683-152411683 - TL53 COSM5751915 c.1308_1309insA p.G437fs*35 Insertion - Frameshift 4:152328317-152328318 - OSCC-GB_01300111 COSM5895337 c.585-5delT p.? Unknown 4:152347076-152347076 - T-LBL-115 COSM33843 c.? p.R465C Substitution - Missense TCGA-60-2698-01 COSM732399 c.2033C>G p.S678* Substitution - Nonsense 4:152322972-152322972 - T368 COSM1052139 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - ME009 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 8016470 COSM1427801 c.1178G>A p.R393Q Substitution - Missense 4:152329730-152329730 - PCSI_0090_Pa_X COSM3380837 c.778T>C p.C260R Substitution - Missense 4:152337885-152337885 - PACA-44-T COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - PD4106a COSM161029 c.244A>T p.N82Y Substitution - Missense 4:152411560-152411560 - CLL035 COSM1291844 c.1790G>A p.G597E Substitution - Missense 4:152324249-152324249 - T1182 COSM4684144 c.529delG p.E177fs*62 Deletion - Frameshift 4:152350097-152350097 - 1219460 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-EK-A2RL-01 COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - T3147 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 8244/9/93C COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-CU-A0YR-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-AP-A056-01 COSM1052110 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - S10-24679-TP COSM4992098 c.1492A>T p.M498L Substitution - Missense 4:152326158-152326158 - 1677162 COSM235639 c.? p.R465L Substitution - Missense YUBER COSM1695076 c.1690C>G p.R564G Substitution - Missense 4:152324349-152324349 - 415 COSM4431374 c.1678G>A p.D560N Substitution - Missense 4:152324361-152324361 - TCGA-CA-6717-01 COSM1427801 c.1178G>A p.R393Q Substitution - Missense 4:152329730-152329730 - ESCC-180T COSM3940773 c.1153A>C p.T385P Substitution - Missense 4:152329755-152329755 - 1115200 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1813501 COSM1155767 c.? p.H535fs*1 Deletion - Frameshift sysucc-834T COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 435 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - PCSI_0284_Pa_P_526 COSM4964444 c.986-1G>A p.? Unknown 4:152330869-152330869 - TCGA-D1-A17Q-01 COSM281108 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - TCGA-AN-A046-01 COSM3825379 c.257C>T p.S86L Substitution - Missense 4:152411547-152411547 - 1116953 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1244707 COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - 1910786 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-CA-6717-01 COSM206732 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 587222 COSM1052109 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - 10-681 COSM1645554 c.1631T>G p.V544G Substitution - Missense 4:152326019-152326019 - 1556231 COSM133115 c.1393_1394CG>TA p.R465Y Substitution - Missense 4:152328232-152328233 - TCGA-EI-6917-01 COSM3428222 c.289G>T p.E97* Substitution - Nonsense 4:152411515-152411515 - 2138891 COSM166364 c.? p.R658* Substitution - Nonsense 1044492 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-AP-A056-01 COSM1052136 c.671G>A p.R224Q Substitution - Missense 4:152346985-152346985 - CR007 COSM302215 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - TCGA-AP-A051-01 COSM1052098 c.1252G>A p.V418M Substitution - Missense 4:152328374-152328374 - DM10 COSM5608727 c.925C>A p.R309S Substitution - Missense 4:152332656-152332656 - 1738939 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TCGA-F5-6814-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - PCSI_0284_Pa_P_526 COSM4964443 c.986-1G>A p.? Unknown 4:152330869-152330869 - 1247755 COSM33844 c.? p.R505C Substitution - Missense 10-396 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2467919 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - HSB2 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - KARPAS-45 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1206645 COSM29552 c.1880T>C p.V627A Substitution - Missense 4:152323125-152323125 - SJTALL003 COSM305939 c.1540G>T p.V514F Substitution - Missense 4:152326110-152326110 - 1677138 COSM33842 c.? p.R465H Substitution - Missense 1247752 COSM33843 c.? p.R465C Substitution - Missense SM98E COSM166365 c.? p.S353fs*24 Unknown 2718 COSM5751153 c.1268G>GT p.V424fs*13 Complex - frameshift 4:152328358-152328358 - TCGA-GN-A266-06 COSM222953 c.1802C>T p.S601F Substitution - Missense 4:152324237-152324237 - 1CM COSM5945942 c.311_313delATG p.H104_A105>P Complex - deletion inframe 4:152411491-152411493 - 1043431 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - PD6944a COSM4383982 c.667C>T p.R223C Substitution - Missense 4:152346989-152346989 - YUSCA COSM5400628 c.1178G>T p.R393L Substitution - Missense 4:152329730-152329730 - SJTALL080 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 587284 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TLE48 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-BS-A0UA-01 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 2492713 COSM5606546 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - TCGA-A5-A0VP-01 COSM1052150 c.40C>T p.R14* Substitution - Nonsense 4:152411764-152411764 - 6597 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - BD49T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1N31-VS-1T31 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1044494 COSM22981 c.936A>C p.R312S Substitution - Missense 4:152332645-152332645 - ICGC_MB74 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3720 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-AH-6897-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-HU-8602-01 COSM271648 c.860A>T p.E287V Substitution - Missense 4:152337803-152337803 - TCGA-B0-5102-01 COSM480960 c.428T>A p.V143D Substitution - Missense 4:152411376-152411376 - TCGA-EI-6917-01 COSM3428223 c.289G>T p.E97* Substitution - Nonsense 4:152411515-152411515 - BD205T COSM5490551 c.1693G>T p.V565F Substitution - Missense 4:152324346-152324346 - TL31 COSM5751238 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - PD9571a COSM5752725 c.145G>T p.E49* Substitution - Nonsense 4:152411659-152411659 - T-LBL-23 COSM33843 c.? p.R465C Substitution - Missense P12-ICHIKAWA COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1735520 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-C5-A1M9-01 COSM4830931 c.1798G>A p.D600N Substitution - Missense 4:152324241-152324241 - 1844281 COSM1169213 c.1444A>C p.T482P Substitution - Missense 4:152326206-152326206 - 2467899 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - C135 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - HCC174 COSM3660929 c.1415A>C p.K472T Substitution - Missense 4:152328211-152328211 - HN_62854 COSM123136 c.994G>A p.E332K Substitution - Missense 4:152330860-152330860 - TCGA-AA-A010-01 COSM281108 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - BD221T COSM5490558 c.1598G>T p.C533F Substitution - Missense 4:152326052-152326052 - 2321312 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-CL-5918-01 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - T3670 COSM320385 c.1847C>T p.T616I Substitution - Missense 4:152324192-152324192 - pfg076T COSM4762877 c.115G>T p.E39* Substitution - Nonsense 4:152411689-152411689 - T1182 COSM4684143 c.529delG p.E177fs*62 Deletion - Frameshift 4:152350097-152350097 - S02344 COSM5693695 c.1248delA p.L417fs*1 Deletion - Frameshift 4:152328378-152328378 - 10539 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - TCGA-BQ-5894-01 COSM3993495 c.643G>A p.A215T Substitution - Missense 4:152347013-152347013 - TCGA-DK-A1AC-01 COSM1309808 c.1637C>T p.S546L Substitution - Missense 4:152326013-152326013 - 2321297 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1874625 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1118431 COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - TCGA-D1-A16Y-01 COSM29768 c.37C>T p.R13* Substitution - Nonsense 4:152411767-152411767 - 1788879 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - OSCC-GB_01310111 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - Co74 COSM33085 c.292C>T p.Q98* Substitution - Nonsense 4:152411512-152411512 - B-ALL4 COSM28797 c.1329_1330ins13 p.K444fs*32 Insertion - Frameshift 4:152328296-152328297 - ESOSCC156T COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - D21 COSM5007904 c.1794_1795insA p.A599fs*6 Insertion - Frameshift 4:152324244-152324245 - S02279 COSM5683771 c.854C>G p.P285R Substitution - Missense 4:152337809-152337809 - D6 COSM5007224 c.2000G>T p.G667V Substitution - Missense 4:152323005-152323005 - SJTALL003 COSM305935 c.1412A>G p.E471G Substitution - Missense 4:152328214-152328214 - 2379661 COSM5031087 c.? p.? Unknown TBR06 COSM1309812 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - 2012-703:2012-1309-T COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - PD10846a COSM5945094 c.685C>T p.Q229* Substitution - Nonsense 4:152346971-152346971 - TCGA-BQ-5894-01 COSM3993496 c.643G>A p.A215T Substitution - Missense 4:152347013-152347013 - SW1463 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 366TS COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - VACO10 COSM287374 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - 428 COSM4433224 c.1855+2delT p.? Unknown 4:152324182-152324182 - sysucc-880T COSM5463321 c.587C>T p.T196I Substitution - Missense 4:152347069-152347069 - T-LBL-19 COSM5885252 c.? p.S426L Substitution - Missense TCGA-AA-3560-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ESCC_124 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2467871 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1115220 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - B110-Tumor COSM1753583 c.873T>A p.Y291* Substitution - Nonsense 4:152332708-152332708 - 3N52-VS-3T52 COSM420169 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - 1813498 COSM1155760 c.? p.D480H Substitution - Missense 1813494 COSM1155768 c.? p.? Unknown 4:152328207-152328207 - HPB-ALL COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - RPMI COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - pfg054T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1114577 COSM27049 c.466C>G p.Q156E Substitution - Missense 4:152411338-152411338 - TCGA-EA-A50E-01 COSM420161 c.963G>A p.W321* Substitution - Nonsense 4:152332618-152332618 - AML_15 COSM732396 c.1963G>T p.E655* Substitution - Nonsense 4:152323042-152323042 - T3724 COSM4684113 c.1617_1618insG p.H540fs*3 Insertion - Frameshift 4:152326032-152326033 - TCGA-D9-A1JW-06 COSM3917250 c.1548T>G p.S516R Substitution - Missense 4:152326102-152326102 - YUBER COSM1695075 c.1690C>G p.R564G Substitution - Missense 4:152324349-152324349 - SNU-C4 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - Au8 COSM5606547 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - 1499689 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 2071415 COSM1732672 c.? p.R505L Substitution - Missense MD-326 COSM302215 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - 2321355 COSM3600936 c.721T>C p.F241L Substitution - Missense 4:152346935-152346935 - T3668 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-AG-A002-01 COSM260908 c.536G>A p.R179H Substitution - Missense 4:152350090-152350090 - 423 COSM1177744 c.1322G>C p.R441P Substitution - Missense 4:152328304-152328304 - T3109 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - pfg181T COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-D5-6927-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-B5-A0JY-01 COSM1052105 c.1144C>A p.H382N Substitution - Missense 4:152329764-152329764 - TCGA-BR-8485-01 COSM4122773 c.1072C>T p.Q358* Substitution - Nonsense 4:152330782-152330782 - PD6171a COSM4385611 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - 587338 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 193 COSM1741800 c.1618C>T p.H540Y Substitution - Missense 4:152326032-152326032 - TCGA-AX-A1C8-01 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 09-664 COSM327079 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - B110 COSM1753583 c.873T>A p.Y291* Substitution - Nonsense 4:152332708-152332708 - SNU-C2B COSM3128005 c.1230A>G p.T410T Substitution - coding silent 4:152329678-152329678 - 193 COSM40079 c.1618C>T p.H540Y Substitution - Missense 4:152326032-152326032 - 112461 COSM22933 c.1947G>A p.W649* Substitution - Nonsense 4:152323058-152323058 - TCGA-14-0817-01 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-33-4583-01 COSM732392 c.1959G>C p.T653T Substitution - coding silent 4:152323046-152323046 - 262LT COSM4168000 c.1390G>A p.V464M Substitution - Missense 4:152328236-152328236 - 1813491 COSM33842 c.? p.R465H Substitution - Missense LUAD-B02515 COSM336211 c.1704_1705GG>TT p.V568>? Complex 4:152324334-152324335 - sysucc-912T COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1813468 COSM33841 c.? p.G423V Substitution - Missense TCGA-02-0010-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - sysucc-1465T COSM4604554 c.1817G>T p.W606L Substitution - Missense 4:152324222-152324222 - 587394 COSM167304 c.1798G>T p.D600Y Substitution - Missense 4:152324241-152324241 - CHC301T COSM3669249 c.1102G>C p.G368R Substitution - Missense 4:152330752-152330752 - TCGA-D5-6531-01 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 2467891 COSM40079 c.1618C>T p.H540Y Substitution - Missense 4:152326032-152326032 - TCGA-A5-A0GP-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3 COSM33763 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 428 COSM4433223 c.1855+2delT p.? Unknown 4:152324182-152324182 - 2138892 COSM33842 c.? p.R465H Substitution - Missense TCGA-18-4083-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 2492721 COSM5723743 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - sysucc-882T COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ESO-601 COSM281109 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - Gp2D COSM1427729 c.1395T>C p.R465R Substitution - coding silent 4:152328231-152328231 - TCGA-D1-A16G-01 COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - 587222 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 6948_PT COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1115205 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD24208a COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - CLL012 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - B22-Tumor COSM30598 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - T3668 COSM4684138 c.1187G>A p.S396N Substitution - Missense 4:152329721-152329721 - 2521259 COSM5895337 c.585-5delT p.? Unknown 4:152347076-152347076 - 1677163 COSM33845 c.? p.R479Q Substitution - Missense TLE84 COSM4167996 c.1578G>A p.W526* Substitution - Nonsense 4:152326072-152326072 - TCGA-AG-3594-01 COSM256127 c.1202_1204delACA p.N401delN Deletion - In frame 4:152329704-152329706 - PD6217a COSM4385612 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - 19 COSM5746359 c.1976A>G p.N659S Substitution - Missense 4:152323029-152323029 - 177-01-9TD COSM673925 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - TCGA-G4-6309-01 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - YUKAT COSM5400634 c.381G>A p.Q127Q Substitution - coding silent 4:152411423-152411423 - 1499690 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ccRCC-64 COSM1659852 c.1636T>C p.S546P Substitution - Missense 4:152326014-152326014 - sysucc-1062T COSM5763423 c.1811A>C p.K604T Substitution - Missense 4:152324228-152324228 - TCGA-14-0817-01 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-AR-A256-01 COSM1052084 c.1634A>G p.Y545C Substitution - Missense 4:152326016-152326016 - TCGA-BS-A0UA-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - LP2000331-DNA_A01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 112503 COSM94296 c.1498C>A p.H500N Substitution - Missense 4:152326152-152326152 - TCGA-A6-5661-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TLE03 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-EK-A3GK-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - ESCC-180T COSM3940772 c.1153A>C p.T385P Substitution - Missense 4:152329755-152329755 - ESCC_BICR_036T COSM5432177 c.1856-2A>G p.? Unknown 4:152323151-152323151 - 2521260 COSM5895336 c.585-5delT p.? Unknown 4:152347076-152347076 - 18 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 381LT COSM4381200 c.285delA p.E96fs*73 Deletion - Frameshift 4:152411519-152411519 - D-06 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 132 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1N31-VS-1T31 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1499694 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 587234 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - S02290 COSM22976 c.1514G>C p.R505P Substitution - Missense 4:152326136-152326136 - 2UM COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD8121a COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 587278 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-D5-6931-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-B0-5400-01 COSM480951 c.2022G>C p.R674R Substitution - coding silent 4:152322983-152322983 - ICGC_MB78 COSM3765114 c.2060G>A p.G687E Substitution - Missense 4:152322945-152322945 - 1677140 COSM33843 c.? p.R465C Substitution - Missense 1738965 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - TLE48 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-G4-6302-01 COSM3696478 c.1606A>C p.T536P Substitution - Missense 4:152326044-152326044 - ESO199PT COSM732380 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 1115497 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AF-2687-01 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - TCGA-AG-A011-01 COSM289997 c.1309G>A p.G437R Substitution - Missense 4:152328317-152328317 - HN_62699 COSM123132 c.1452G>T p.R484S Substitution - Missense 4:152326198-152326198 - TCGA-AM-5820-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - SK-OV-3 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - TCGA-CG-5733-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HN122PT COSM99621 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - TLE48 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - ESO199PT COSM33763 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 8067521 COSM1427762 c.1313C>A p.S438Y Substitution - Missense 4:152328313-152328313 - 1813470 COSM1155749 c.? p.R441Q Substitution - Missense CHC301T COSM3669250 c.1102G>C p.G368R Substitution - Missense 4:152330752-152330752 - PACA46 COSM1158149 c.1338G>T p.W446C Substitution - Missense 4:152328288-152328288 - TCGA-AX-A0J0-01 COSM206687 c.1973G>A p.R658Q Substitution - Missense 4:152323032-152323032 - TCGA-EA-A3QE-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2467897 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T1184 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-BS-A0UA-01 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-BR-8360-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1738969 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - T3109 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 2467867 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 112497 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - HSB2 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - LUAD-B02515 COSM336210 c.1704_1705GG>TT p.V568>? Complex 4:152324334-152324335 - TCGA-AA-A024-01 COSM287374 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - P6 COSM287374 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - 2274324 COSM4413603 c.1552G>A p.A518T Substitution - Missense 4:152326098-152326098 - TCGA-Q1-A73O-01 COSM4834126 c.829C>G p.Q277E Substitution - Missense 4:152337834-152337834 - 6115227 COSM5568921 c.256T>G p.S86A Substitution - Missense 4:152411548-152411548 - 4752 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 4084 COSM5751238 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - 1118432 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - 85T COSM302217 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - 60T COSM110669 c.1777_1778insT p.L594fs*11 Insertion - Frameshift 4:152324261-152324262 - B110-Tumor COSM1753582 c.873T>A p.Y291* Substitution - Nonsense 4:152332708-152332708 - TLE48 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1115503 COSM27055 c.1510G>A p.V504I Substitution - Missense 4:152326140-152326140 - DLBCL689 COSM1580889 c.479C>T p.P160L Substitution - Missense 4:152411325-152411325 - TCGA-A6-3807-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1219469 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AA-3672-01 COSM24620 c.1417delA p.R473fs*25 Deletion - Frameshift 4:152328209-152328209 - 415 COSM4431375 c.1678G>A p.D560N Substitution - Missense 4:152324361-152324361 - 10539 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - S02344 COSM5693694 c.1248delA p.L417fs*1 Deletion - Frameshift 4:152328378-152328378 - YUKAT COSM3127901 c.2019G>A p.W673* Substitution - Nonsense 4:152322986-152322986 - 2138881 COSM87015 c.? p.R278* Substitution - Nonsense HT115 COSM206731 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - TCGA-BR-8380-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - SJHYPO119 COSM4775963 c.1237-2A>G p.? Unknown 4:152328391-152328391 - 1788878 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2083419 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-AX-A05Z-01 COSM1052145 c.403G>T p.D135Y Substitution - Missense 4:152411401-152411401 - RMH-1549 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 8035729 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - DM851T COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - 196 COSM27400 c.1158C>G p.C386W Substitution - Missense 4:152329750-152329750 - pfg220T COSM4762865 c.1275G>A p.W425* Substitution - Nonsense 4:152328351-152328351 - TL87 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 127T COSM302217 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - DLBCL689 COSM1580890 c.479C>T p.P160L Substitution - Missense 4:152411325-152411325 - 1115221 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ME009T COSM222959 c.1685C>T p.S562L Substitution - Missense 4:152324354-152324354 - PD9571a COSM5752726 c.145G>T p.E49* Substitution - Nonsense 4:152411659-152411659 - TCGA-21-1078-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - RMS2107 COSM5880989 c.1100G>C p.R367P Substitution - Missense 4:152330754-152330754 - 2083406 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 86331 COSM96316 c.1267G>A p.G423R Substitution - Missense 4:152328359-152328359 - TCGA-25-1316-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 587302 COSM1206893 c.1625A>T p.N542I Substitution - Missense 4:152326025-152326025 - BD44T COSM5490535 c.1607C>A p.T536K Substitution - Missense 4:152326043-152326043 - 10-54 COSM1645394 c.1812A>C p.K604N Substitution - Missense 4:152324227-152324227 - ICGC_MB74 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2011-2324:2012-339-T COSM22931 c.1318G>A p.D440N Substitution - Missense 4:152328308-152328308 - TCGA-22-1012-01 COSM732395 c.1963G>T p.E655* Substitution - Nonsense 4:152323042-152323042 - sysucc-1317T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - CTV1 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1116998 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AR-A256-01 COSM22989 c.1634A>G p.Y545C Substitution - Missense 4:152326016-152326016 - 1813490 COSM33842 c.? p.R465H Substitution - Missense TCGA-AA-A01Z-01 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - SJTALL003 COSM305941 c.1540G>T p.V514F Substitution - Missense 4:152326110-152326110 - TCGA-AC-A2QI-01 COSM3825382 c.38G>T p.R13L Substitution - Missense 4:152411766-152411766 - 2492711 COSM5606547 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - ESCC_38 COSM27050 c.1780C>T p.L594F Substitution - Missense 4:152324259-152324259 - HN_62854 COSM123138 c.994G>A p.E332K Substitution - Missense 4:152330860-152330860 - T-LBL-32 COSM5885251 c.? p.V424L Substitution - Missense TCGA-G2-A2ES-01 COSM1309812 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - 2083405 COSM1738001 c.2013_2014insGGGGAGTT p.V672fs*38 Insertion - Frameshift 4:152322991-152322992 - T2647 COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - TCGA-D1-A16I-01 COSM1052121 c.802_803delAT p.M268fs*18 Deletion - Frameshift 4:152337860-152337861 - 2083392 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 609 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-EI-6507-01 COSM1566943 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - TCGA-BR-7851-01 COSM4122749 c.1876G>A p.A626T Substitution - Missense 4:152323129-152323129 - 2011-2293:2012-1333-T COSM4604553 c.1817G>T p.W606L Substitution - Missense 4:152324222-152324222 - PD5725a COSM4385612 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - T-LBL-94 COSM5885255 c.? p.G477V Substitution - Missense 339 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1219468 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T-ALL5 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1044506 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-AA-3681-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T3535 COSM24620 c.1417delA p.R473fs*25 Deletion - Frameshift 4:152328209-152328209 - TCGA-02-0028-01 COSM35614 c.2014G>A p.V672M Substitution - Missense 4:152322991-152322991 - TCGA-DS-A1OA-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-AG-3725-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 1N52-VS-1T52 COSM123130 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - ESCC_131 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - SJTALL003 COSM305937 c.1412A>G p.E471G Substitution - Missense 4:152328214-152328214 - 1247762 COSM33842 c.? p.R465H Substitution - Missense 10-681 COSM1645553 c.1631T>G p.V544G Substitution - Missense 4:152326019-152326019 - T-LBL-74 COSM5885262 c.? p.R689W Substitution - Missense JURKAT COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-D8-A1XK-01 COSM3825376 c.529G>A p.E177K Substitution - Missense 4:152350097-152350097 - TCGA-FS-A1YY-06 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-CG-5723-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1738976 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - HCA7 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - TCGA-51-4081-01 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - ESO-601 COSM281108 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - T3151 COSM4684129 c.1275G>T p.W425C Substitution - Missense 4:152328351-152328351 - TCGA-GN-A262-06 COSM3600911 c.1632C>G p.V544V Substitution - coding silent 4:152326018-152326018 - 9835 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - PEER COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2011-2265:2012-367-T COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 1813477 COSM33843 c.? p.R465C Substitution - Missense 1738942 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - T3306 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 8035729 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2011-2293:2012-1333-T COSM4604554 c.1817G>T p.W606L Substitution - Missense 4:152324222-152324222 - TCGA-E2-A15L-01 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - 2321333 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - PD4100a COSM161027 c.254T>G p.I85S Substitution - Missense 4:152411550-152411550 - HN33PT COSM100044 c.983_984insA p.I330fs*2 Insertion - Frameshift 4:152332597-152332598 - HPB-ALL COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 10-76 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ESCC-059T COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - SNU-C4 COSM1566943 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - 3_RESISTANT COSM1723800 c.979delG p.E327fs*15 Deletion - Frameshift 4:152332602-152332602 - TCGA-BF-A3DL-01 COSM4904812 c.1117C>T p.P373S Substitution - Missense 4:152330737-152330737 - 2012-703:2012-1309-T COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - TCGA-DK-A2I2-01 COSM732399 c.2033C>G p.S678* Substitution - Nonsense 4:152322972-152322972 - TCGA-D5-6531-01 COSM5163239 c.1161_1162insA p.Q388fs*5 Insertion - Frameshift 4:152329746-152329747 - 192T COSM51395 c.490A>T p.K164* Substitution - Nonsense 4:152411314-152411314 - 10059 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2321333 COSM4775050 c.1436_1437insT p.D480fs*5 Insertion - Frameshift 4:152326213-152326214 - 1219463 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - DM851T COSM673925 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - 2467882 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3094 COSM4684092 c.2054C>A p.A685E Substitution - Missense 4:152322951-152322951 - TCGA-FI-A2EX-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1813499 COSM33844 c.? p.R505C Substitution - Missense CCK81 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-18-3409-01 COSM732370 c.535C>T p.R179C Substitution - Missense 4:152350091-152350091 - 185T COSM4385943 c.1333_1334insA p.V445fs*27 Insertion - Frameshift 4:152328292-152328293 - 10234 COSM5751238 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - 1044493 COSM22980 c.907C>T p.Q303* Substitution - Nonsense 4:152332674-152332674 - 2389307 COSM28490 c.? p.? Unknown 1738962 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - TCGA-AA-A024-01 COSM133117 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - HN33PT COSM100042 c.983_984insA p.I330fs*2 Insertion - Frameshift 4:152332597-152332598 - T1 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BT-A0YX-01 COSM420165 c.1277C>T p.S426L Substitution - Missense 4:152328349-152328349 - T3668 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - T2991 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TBR03 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - Mx35 COSM50228 c.388_389insCTGAT p.D130fs*41 Insertion - Frameshift 4:152411411-152411412 - TCGA-BK-A13C-01 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 1116986 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 424 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TBR03 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TL26 COSM5751728 c.664C>CT p.R222fs*34 Complex - frameshift 4:152346992-152346992 - P8 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - BL-18 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-F1-A448-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3658 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3535 COSM292754 c.1417delA p.R473fs*25 Deletion - Frameshift 4:152328209-152328209 - STC246 COSM1052092 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - 2535928 COSM33845 c.? p.R479Q Substitution - Missense 1738940 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - TCGA-D1-A17A-01 COSM1052142 c.415C>A p.H139N Substitution - Missense 4:152411389-152411389 - 587278 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-B0-4706-01 COSM480956 c.1761G>A p.M587I Substitution - Missense 4:152324278-152324278 - CSCC-60-T COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - 15935P COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T2621 COSM4684096 c.1876G>C p.A626P Substitution - Missense 4:152323129-152323129 - 1494 COSM22977 c.1787C>T p.S596F Substitution - Missense 4:152324252-152324252 - T3094 COSM4684119 c.1381A>G p.T461A Substitution - Missense 4:152328245-152328245 - 13854/93C COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1874633 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - LUAD-S01306 COSM343648 c.1617G>A p.G539G Substitution - coding silent 4:152326033-152326033 - ESO-327 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 1953_T COSM3946067 c.127C>A p.Q43K Substitution - Missense 4:152411677-152411677 - 2011-2324:2012-339-T COSM4604261 c.1318G>A p.D440N Substitution - Missense 4:152328308-152328308 - sysucc-1062T COSM5763422 c.1811A>C p.K604T Substitution - Missense 4:152324228-152324228 - 7192 COSM5751359 c.2065C>CT p.R689fs*5 Complex - frameshift 4:152322940-152322940 - sysucc-1317T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-C4-A0F1-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - SJRHB048 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-D5-6928-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-66-2744-01 COSM732372 c.1368C>A p.T456T Substitution - coding silent 4:152328258-152328258 - Pat_26_A COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - TCGA-AG-A002-01 COSM260909 c.536G>A p.R179H Substitution - Missense 4:152350090-152350090 - TCGA-C5-A1BJ-01 COSM420169 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - D21 COSM5007908 c.1329delC p.V445fs*53 Deletion - Frameshift 4:152328297-152328297 - 363 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 10-661 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - S671 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-B5-A0JV-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD7721a COSM4604317 c.1394G>C p.R465P Substitution - Missense 4:152328232-152328232 - T2769 COSM4745532 c.1335_1336GT>TG p.W446G Substitution - Missense 4:152328290-152328291 - 1043436 COSM28490 c.? p.? Unknown TCGA-EK-A2R7-01 COSM4852255 c.1798G>C p.D600H Substitution - Missense 4:152324241-152324241 - 180 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-02-0028-01 COSM1559697 c.2014G>A p.V672M Substitution - Missense 4:152322991-152322991 - P0004 COSM5885191 c.? p.Q47* Substitution - Nonsense TLE03 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJHYPO119 COSM4775962 c.1237-2A>G p.? Unknown 4:152328391-152328391 - 284A COSM22972 c.845C>A p.S282* Substitution - Nonsense 4:152337818-152337818 - 2748 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - JURKAT COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ME009T COSM222955 c.1802C>T p.S601F Substitution - Missense 4:152324237-152324237 - CSCC-62-T COSM4448895 c.1419-2A>C p.? Unknown 4:152326233-152326233 - 1044739 COSM22934 c.1996delG p.S668fs*39 Deletion - Frameshift 4:152323009-152323009 - TL43 COSM5751877 c.984_985insA p.G329fs*3 Insertion - Frameshift 4:152332596-152332597 - TCGA-AY-6386-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 587226 COSM1206887 c.1409A>G p.H470R Substitution - Missense 4:152328217-152328217 - HN112PT COSM99188 c.556_559delAAAC p.K186fs*52 Deletion - Frameshift 4:152350067-152350070 - TCGA-D1-A16Y-01 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1990388 COSM420169 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - 1738937 COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - 1247761 COSM33846 c.? p.R479L Substitution - Missense HPB_ALL COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - Jurkat COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PD2754a COSM27914 c.2001_2002insG p.S668fs*26 Insertion - Frameshift 4:152323003-152323004 - 1219474 COSM30602 c.1744T>C p.S582P Substitution - Missense 4:152324295-152324295 - 428 COSM4433229 c.1855+1G>A p.? Unknown 4:152324183-152324183 - D13 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TCGA-D1-A160-01 COSM1052147 c.386A>C p.D129A Substitution - Missense 4:152411418-152411418 - T3049 COSM4684133 c.1202A>G p.N401S Substitution - Missense 4:152329706-152329706 - 4752 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - TCGA-G4-6302-01 COSM3696479 c.1606A>C p.T536P Substitution - Missense 4:152326044-152326044 - T3038 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - sysucc-834T COSM5486404 c.1852C>T p.Q618* Substitution - Nonsense 4:152324187-152324187 - TCGA-AD-6889-01 COSM1427914 c.277G>T p.G93* Substitution - Nonsense 4:152411527-152411527 - ICGC_MB518 COSM306982 c.726+1G>A p.? Unknown 4:152346929-152346929 - D6 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1556262 COSM133116 c.1329_1330insGG p.K444fs*55 Insertion - Frameshift 4:152328296-152328297 - B106 COSM1753572 c.1590T>G p.T530T Substitution - coding silent 4:152326060-152326060 - PD4002a COSM161024 c.1322G>T p.R441L Substitution - Missense 4:152328304-152328304 - 1206697 COSM29554 c.1958delC p.T653fs*8 Deletion - Frameshift 4:152323047-152323047 - TCGA-EK-A3GN-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJTALL003 COSM305951 c.1411G>T p.E471* Substitution - Nonsense 4:152328215-152328215 - sysucc-1465T COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HT115 COSM281109 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - 2321324 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - Hx218 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 2201859 COSM22937 c.349_351delGAG p.E117del Deletion - In frame 4:152411453-152411455 - ESCC-F75 COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - 394 COSM3721799 c.1631T>A p.V544D Substitution - Missense 4:152326019-152326019 - 1813471 COSM1155756 c.? p.W446* Substitution - Nonsense S09-31237-TP COSM4992103 c.555G>A p.K185K Substitution - coding silent 4:152350071-152350071 - 1735528 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BR-7851-01 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - T11 COSM5344639 c.1496G>T p.G499V Substitution - Missense 4:152326154-152326154 - SJTALL080 COSM4603680 c.?_?ins? p.E327fs Insertion - Frameshift TL87 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1995676 COSM33841 c.? p.G423V Substitution - Missense DLBCL922 COSM1580891 c.302A>T p.D101V Substitution - Missense 4:152411502-152411502 - DM10 COSM5608722 c.1690C>A p.R564S Substitution - Missense 4:152324349-152324349 - HT115 COSM281108 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - 1735494 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 77 COSM96473 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - JURKAT COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-E6-A1LZ-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - BD44T COSM5490534 c.1607C>A p.T536K Substitution - Missense 4:152326043-152326043 - 1677161 COSM235640 c.? p.W425S Substitution - Missense 2542193 COSM33845 c.? p.R479Q Substitution - Missense 1043435 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - SJTALL003 COSM305935 c.1412A>G p.E471G Substitution - Missense 4:152328214-152328214 - PD2732a COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1118429 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 1874642 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-AC-A2QI-01 COSM3825381 c.38G>T p.R13L Substitution - Missense 4:152411766-152411766 - 27 COSM5748787 c.1319A>T p.D440V Substitution - Missense 4:152328307-152328307 - 2492714 COSM5606546 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - 3940 COSM5751206 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - CSCC-17-T COSM4510948 c.852C>T p.L284L Substitution - coding silent 4:152337811-152337811 - TCGA-A5-A0R8-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T3502 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1044385 COSM22998 c.540delT p.S182fs*57 Deletion - Frameshift 4:152350086-152350086 - 1N47-VS-1T47 COSM4976335 c.1090_1093delAACT p.N364fs*12 Deletion - Frameshift 4:152330761-152330764 - 1500571 COSM33845 c.? p.R479Q Substitution - Missense LUAD-LIP77 COSM342477 c.631G>A p.D211N Substitution - Missense 4:152347025-152347025 - 3N57-VS-3T57 COSM4984008 c.763G>T p.E255* Substitution - Nonsense 4:152337900-152337900 - RMS240 COSM5686715 c.1514G>C p.R505P Substitution - Missense 4:152326136-152326136 - 3988 COSM5751153 c.1268G>GT p.V424fs*13 Complex - frameshift 4:152328358-152328358 - 299 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2011-2265:2012-367-T COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-BL-A13I-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 234 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SCC COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - ESCC_11 COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - 1116983 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - Jurkat COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-14-0817 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1219467 COSM30598 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - 2471671 COSM33842 c.? p.R465H Substitution - Missense 522_T COSM3127945 c.1735G>T p.G579W Substitution - Missense 4:152324304-152324304 - 2521330 COSM1566938 c.1327C>T p.L443F Substitution - Missense 4:152328299-152328299 - TCGA-18-3406-01 COSM732388 c.1754G>C p.S585T Substitution - Missense 4:152324285-152324285 - 7192 COSM5751360 c.2065C>CT p.R689fs*5 Complex - frameshift 4:152322940-152322940 - SJTALL003 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D1-A0ZP-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJTALL003 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2321312 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - S848 COSM420169 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - 1247757 COSM33844 c.? p.R505C Substitution - Missense T47 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - RMS240 COSM22976 c.1514G>C p.R505P Substitution - Missense 4:152326136-152326136 - 9967 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 195 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-BT-A0YX-01 COSM420166 c.1277C>T p.S426L Substitution - Missense 4:152328349-152328349 - 2321297 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HT115 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1247758 COSM33845 c.? p.R479Q Substitution - Missense 1115058 COSM27053 c.791A>G p.Q264R Substitution - Missense 4:152337872-152337872 - TCGA-EE-A2A2-06 COSM3600945 c.358C>T p.Q120* Substitution - Nonsense 4:152411446-152411446 - 10-661 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - SJTALL003 COSM305941 c.1540G>T p.V514F Substitution - Missense 4:152326110-152326110 - ESCC-F20 COSM5047307 c.1220C>A p.S407* Substitution - Nonsense 4:152329688-152329688 - 2492714 COSM5606547 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - PACA44 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 1910786 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - ESCC-205T COSM3940768 c.1310G>A p.G437E Substitution - Missense 4:152328316-152328316 - TL43 COSM5751876 c.984_985insA p.G329fs*3 Insertion - Frameshift 4:152332596-152332597 - CML-T1 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2083389 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-C4-A0F0-01 COSM420161 c.963G>A p.W321* Substitution - Nonsense 4:152332618-152332618 - DM10 COSM161026 c.1322G>T p.R441L Substitution - Missense 4:152328304-152328304 - TCGA-A6-2677-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 09-664 COSM327081 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - TCGA-BK-A0CA-01 COSM1052087 c.1427G>T p.S476I Substitution - Missense 4:152326223-152326223 - B106-Tumor COSM1753572 c.1590T>G p.T530T Substitution - coding silent 4:152326060-152326060 - B89-10 COSM1753577 c.1311A>T p.G437G Substitution - coding silent 4:152328315-152328315 - T36 COSM3127925 c.1877C>T p.A626V Substitution - Missense 4:152323128-152323128 - TCGA-EI-6507-01 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - TCGA-D1-A16G-01 COSM1052102 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - Gp5D COSM1427728 c.1395T>C p.R465R Substitution - coding silent 4:152328231-152328231 - PD6187a COSM4385611 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - LIM2551 COSM4644585 c.1732A>C p.T578P Substitution - Missense 4:152324307-152324307 - CR007 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - HCC2998 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 2788 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-EO-A1Y5-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - B22 COSM30598 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - TCGA-GN-A266-06 COSM222955 c.1802C>T p.S601F Substitution - Missense 4:152324237-152324237 - PT15_1 COSM5895337 c.585-5delT p.? Unknown 4:152347076-152347076 - I2L-P24Ta-Tumor-Biopsy COSM5355755 c.501delA p.M168fs*1 Deletion - Frameshift 4:152411303-152411303 - ESCC_118 COSM5640305 c.1922C>G p.S641* Substitution - Nonsense 4:152323083-152323083 - TLE43 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TL19 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1556292 COSM133115 c.1393_1394CG>TA p.R465Y Substitution - Missense 4:152328232-152328233 - 1219472 COSM30600 c.1595C>A p.T532N Substitution - Missense 4:152326055-152326055 - LUAD-F00057 COSM22388 c.328G>T p.E110* Substitution - Nonsense 4:152411476-152411476 - D13 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - pfg220T COSM4762864 c.1275G>A p.W425* Substitution - Nonsense 4:152328351-152328351 - PD8500a COSM5945074 c.1553C>T p.A518V Substitution - Missense 4:152326097-152326097 - 1044499 COSM22985 c.1313C>T p.S438F Substitution - Missense 4:152328313-152328313 - pfg016T COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - 1044491 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - CLL035 COSM1291843 c.1790G>A p.G597E Substitution - Missense 4:152324249-152324249 - PDA_105 COSM5003733 c.1786T>G p.S596A Substitution - Missense 4:152324253-152324253 - sysucc-1484T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AA-3852-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1788880 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1218263 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 900T COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - Region-27 COSM5748991 c.598G>T p.V200L Substitution - Missense 4:152347058-152347058 - 2138883 COSM33845 c.? p.R479Q Substitution - Missense T-LBL-8 COSM33843 c.? p.R465C Substitution - Missense TCGA-CG-4305-01 COSM4122753 c.1677T>C p.L559L Substitution - coding silent 4:152324362-152324362 - 100924 COSM94299 c.1229C>T p.T410I Substitution - Missense 4:152329679-152329679 - J57_T COSM3946062 c.829C>T p.Q277* Substitution - Nonsense 4:152337834-152337834 - DLBCL737 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD2737a COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - YULAN COSM1695086 c.1118C>T p.P373L Substitution - Missense 4:152330736-152330736 - sysucc-771T COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 3N52-VS-3T52 COSM420170 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - HN122PT COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - BE-13 COSM27062 c.?_?del? p.? Unknown 1524378 COSM96473 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - TCGA-D5-6927-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PCSI_0103_Pa_P COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-D1-A0ZP-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HT115 COSM206732 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - T3668 COSM4684139 c.1187G>A p.S396N Substitution - Missense 4:152329721-152329721 - 112377 COSM94292 c.1555T>G p.Y519D Substitution - Missense 4:152326095-152326095 - 428 COSM4433228 c.1855+1G>A p.? Unknown 4:152324183-152324183 - B22-Tumor COSM300416 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - TCGA-AA-A01Z-01 COSM300416 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - 09-3 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - CR007 COSM302217 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - TCGA-BR-4362-01 COSM4122784 c.242A>G p.N81S Substitution - Missense 4:152411562-152411562 - TCGA-BR-7851-01 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - T407 COSM4684102 c.1817G>A p.W606* Substitution - Nonsense 4:152324222-152324222 - TCGA-DC-6682-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TL53 COSM5751916 c.1308_1309insA p.G437fs*35 Insertion - Frameshift 4:152328317-152328318 - 1116995 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1116949 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-CA-6717-01 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-AY-6386-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - CCRF-CEM COSM327075 c.2054C>T p.A685V Substitution - Missense 4:152322951-152322951 - TCGA-85-6561-01 COSM732376 c.1435C>A p.R479R Substitution - coding silent 4:152326215-152326215 - T2621 COSM4684097 c.1876G>C p.A626P Substitution - Missense 4:152323129-152323129 - T-LBL-96 COSM33842 c.? p.R465H Substitution - Missense T-LBL-3 COSM33843 c.? p.R465C Substitution - Missense TCGA-AH-6903-01 COSM1052139 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - TCGA-HU-8602-01 COSM271650 c.860A>T p.E287V Substitution - Missense 4:152337803-152337803 - TCGA-AP-A0LM-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - S02279 COSM5683770 c.854C>G p.P285R Substitution - Missense 4:152337809-152337809 - T-LBL-73 COSM33841 c.? p.G423V Substitution - Missense 1044740 COSM22935 c.2021G>A p.R674Q Substitution - Missense 4:152322984-152322984 - AML_535 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-AG-A011-01 COSM289999 c.1309G>A p.G437R Substitution - Missense 4:152328317-152328317 - TLE36 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - LUAD-B01145 COSM333438 c.303T>A p.D101E Substitution - Missense 4:152411501-152411501 - TL89 COSM5751206 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - ICGC_MB74 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2321324 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-02-0010-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TLE48 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - ICC014T COSM5823614 c.333G>T p.E111D Substitution - Missense 4:152411471-152411471 - 4084 COSM5751242 c.121C>CT p.Q41fs*18 Complex - frameshift 4:152411683-152411683 - ESO156PT COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - T3454 COSM4684123 c.1347_1348delGA p.E449fs*22 Deletion - Frameshift 4:152328278-152328279 - 1116966 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2083411 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - JM COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 18 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2389309 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - 587338 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AG-3898-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - JURKAT COSM327083 c.930C>T p.Y310Y Substitution - coding silent 4:152332651-152332651 - TCGA-AA-3831-01 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 07-058 COSM3736337 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - S02249 COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - J57_T COSM3946061 c.829C>T p.Q277* Substitution - Nonsense 4:152337834-152337834 - 2492720 COSM5723744 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - ATL030 COSM5709105 c.639A>C p.R213S Substitution - Missense 4:152347017-152347017 - XHDG17 COSM27052 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - 2321333 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - SJRHB048 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 15 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-GM-A2D9-01 COSM3825366 c.1011G>A p.K337K Substitution - coding silent 4:152330843-152330843 - D-06 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - sysucc-1484T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-DG-A2KK-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-60-2722-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-EE-A29D-06 COSM3600922 c.1267G>T p.G423* Substitution - Nonsense 4:152328359-152328359 - 2138888 COSM3718365 c.? p.E192A Substitution - Missense TCGA-BS-A0U8-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-D1-A16X-01 COSM302217 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - TBR06 COSM1309813 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - 1191-01-02TD COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - SW48 COSM3128081 c.456G>A p.L152L Substitution - coding silent 4:152411348-152411348 - 175 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD9384a COSM5945079 c.1276T>C p.S426P Substitution - Missense 4:152328350-152328350 - 1874647 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1118426 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - HCC174 COSM3660930 c.1415A>C p.K472T Substitution - Missense 4:152328211-152328211 - CTV1 COSM327081 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - 1244718 COSM33763 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 587260 COSM1206883 c.770T>A p.I257N Substitution - Missense 4:152337893-152337893 - YUKAT COSM5400633 c.381G>A p.Q127Q Substitution - coding silent 4:152411423-152411423 - ME009T COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - MD-326 COSM302217 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - SM88 COSM166364 c.? p.R658* Substitution - Nonsense 587348 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - PD2740a COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1044502 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - K419 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - Pat_76_A COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TCGA-51-4081-01 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - 2138879 COSM3718360 c.? p.W244* Substitution - Nonsense 2159492 COSM96316 c.1267G>A p.G423R Substitution - Missense 4:152328359-152328359 - 1990387 COSM27054 c.1556A>G p.Y519C Substitution - Missense 4:152326094-152326094 - CCRF-CEM COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 423 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - HN_00338 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - T80 COSM1177745 c.1322G>C p.R441P Substitution - Missense 4:152328304-152328304 - 2073882 COSM33842 c.? p.R465H Substitution - Missense 1044497 COSM22983 c.1190G>A p.G397D Substitution - Missense 4:152329718-152329718 - TL28 COSM5751740 c.1061C>CT p.Y355fs*8 Complex - frameshift 4:152330793-152330793 - SJHGG109_A COSM4971902 c.780T>A p.C260* Substitution - Nonsense 4:152337883-152337883 - TCGA-CM-4744-01 COSM1427787 c.1259_1260insGTGGGACA p.H420fs*13 Insertion - Frameshift 4:152328366-152328367 - 2157490 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 11114 COSM5751237 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - TCGA-BS-A0UA-01 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - T3499 COSM4684107 c.1738C>G p.H580D Substitution - Missense 4:152324301-152324301 - 1738936 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 205881 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - TCGA-G4-6293-01 COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - 1218267 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2083387 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - KARPAS-45 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-CG-5723-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 587376 COSM1052137 c.671G>A p.R224Q Substitution - Missense 4:152346985-152346985 - ESCC_6 COSM4762876 c.115G>T p.E39* Substitution - Nonsense 4:152411689-152411689 - TCGA-D1-A15X-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BR-7851-01 COSM4122748 c.1876G>A p.A626T Substitution - Missense 4:152323129-152323129 - 1556246 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 86507 COSM94294 c.1526A>T p.Y509F Substitution - Missense 4:152326124-152326124 - TCGA-AG-3742-01 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TCGA-A6-6137-01 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - PD2727a COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - ZZUFHECRKL-G067T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1813497 COSM1155759 c.? p.R479P Substitution - Missense DLBCL834 COSM96473 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - 09-297 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - SKOV3 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - 1219464 COSM30596 c.893C>G p.P298R Substitution - Missense 4:152332688-152332688 - TCGA-BS-A0UA-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 6115227 COSM5568922 c.256T>G p.S86A Substitution - Missense 4:152411548-152411548 - 19 COSM5746360 c.1976A>G p.N659S Substitution - Missense 4:152323029-152323029 - T-LBL-45 COSM5885261 c.? p.D642fs*15 Frameshift T-LBL-116 COSM5885259 c.? p.Y519C Substitution - Missense 2138890 COSM33845 c.? p.R479Q Substitution - Missense TCGA-BK-A0CA-01 COSM1052088 c.1427G>T p.S476I Substitution - Missense 4:152326223-152326223 - OSCC-GB_00240111 COSM22936 c.2077G>A p.E693K Substitution - Missense 4:152322928-152322928 - TCGA-AX-A0J0-01 COSM1052126 c.744G>T p.E248D Substitution - Missense 4:152337919-152337919 - TCGA-AH-6897-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - DM45 COSM5611283 c.180_181TG>GT p.G61* Substitution - Nonsense 4:152411623-152411624 - 1115499 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - P6 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - HN_62699 COSM123134 c.1452G>T p.R484S Substitution - Missense 4:152326198-152326198 - JURKAT COSM327085 c.930C>T p.Y310Y Substitution - coding silent 4:152332651-152332651 - D13 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 2432702 COSM28490 c.? p.? Unknown TCGA-FU-A57G-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - CHC327T COSM4957966 c.1272A>G p.V424V Substitution - coding silent 4:152328354-152328354 - 262LT COSM4168001 c.1390G>A p.V464M Substitution - Missense 4:152328236-152328236 - 2138893 COSM3718363 c.? p.E113D Substitution - Missense 109T COSM22978 c.658C>T p.Q220* Substitution - Nonsense 4:152346998-152346998 - XHDG17C COSM4767557 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - 09-3 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AA-3848-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJTALL003 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 8044826 COSM1158148 c.1338G>T p.W446C Substitution - Missense 4:152328288-152328288 - 1115500 COSM27057 c.943G>A p.A315T Substitution - Missense 4:152332638-152332638 - 1114578 COSM27050 c.1780C>T p.L594F Substitution - Missense 4:152324259-152324259 - T3658 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - Hx174 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-D1-A17Q-01 COSM1052133 c.711G>A p.W237* Substitution - Nonsense 4:152346945-152346945 - TCGA-BR-8487-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-BS-A0UA-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-EK-A3GN-01 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - LIM2551 COSM4644584 c.1732A>C p.T578P Substitution - Missense 4:152324307-152324307 - T-LBL-80 COSM33845 c.? p.R479Q Substitution - Missense 10-671 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AA-3837-01 COSM271650 c.860A>T p.E287V Substitution - Missense 4:152337803-152337803 - 8044826 COSM1158149 c.1338G>T p.W446C Substitution - Missense 4:152328288-152328288 - TCGA-AX-A1C8-01 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-AG-3725-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 105225 COSM94301 c.985G>T p.G329W Substitution - Missense 4:152332596-152332596 - TCGA-AA-A010-01 COSM281109 c.432G>A p.T144T Substitution - coding silent 4:152411372-152411372 - SNU-C2B COSM3128004 c.1230A>G p.T410T Substitution - coding silent 4:152329678-152329678 - ESCC_BICR_036T COSM5432178 c.1856-2A>G p.? Unknown 4:152323151-152323151 - 1874637 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 4132_T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TLE83 COSM4168000 c.1390G>A p.V464M Substitution - Missense 4:152328236-152328236 - CRC-10T COSM5457710 c.584+1G>T p.? Unknown 4:152350041-152350041 - TCGA-BR-8485-01 COSM4122774 c.1072C>T p.Q358* Substitution - Nonsense 4:152330782-152330782 - T3724 COSM4684112 c.1617_1618insG p.H540fs*3 Insertion - Frameshift 4:152326032-152326033 - 10246 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - DM10 COSM161024 c.1322G>T p.R441L Substitution - Missense 4:152328304-152328304 - RMS2107 COSM5880990 c.1100G>C p.R367P Substitution - Missense 4:152330754-152330754 - TCGA-BR-4362-01 COSM4122783 c.242A>G p.N81S Substitution - Missense 4:152411562-152411562 - 1116985 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1044513 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - XHDG17 COSM4767557 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - 1116935 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - CHC327T COSM4957965 c.1272A>G p.V424V Substitution - coding silent 4:152328354-152328354 - TCGA-BR-8487-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2138882 COSM33844 c.? p.R505C Substitution - Missense Br27P COSM40079 c.1618C>T p.H540Y Substitution - Missense 4:152326032-152326032 - XHDG53C COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1713272 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1874650 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - sysucc-1397T COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 339 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ESCC_BICR_045T COSM123130 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - T3498 COSM1566943 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - 01-P8014 COSM4584838 c.321A>G p.E107E Substitution - coding silent 4:152411483-152411483 - YUSCA COSM5400629 c.1178G>T p.R393L Substitution - Missense 4:152329730-152329730 - DM1 COSM5608717 c.1675C>T p.L559F Substitution - Missense 4:152324364-152324364 - 10175 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1043433 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - Pat_76_A COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 46M COSM5587805 c.2009G>A p.G670E Substitution - Missense 4:152322996-152322996 - 1788877 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 1044498 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - T3720 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - T12 COSM5344634 c.1931G>A p.G644E Substitution - Missense 4:152323074-152323074 - TCGA-E2-A574-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1556252 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD2722a COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1044496 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 205881 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - TCGA-EK-A2PL-01 COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - HCC174T COSM3660930 c.1415A>C p.K472T Substitution - Missense 4:152328211-152328211 - T368 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - 587222 COSM1052110 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - ATL030 COSM5709104 c.639A>C p.R213S Substitution - Missense 4:152347017-152347017 - pfg127T COSM4762860 c.1508C>T p.A503V Substitution - Missense 4:152326142-152326142 - 526T COSM306984 c.726+1G>A p.? Unknown 4:152346929-152346929 - 1N52-VS-1T52 COSM123128 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - TCGA-EK-A2R7-01 COSM4852256 c.1798G>C p.D600H Substitution - Missense 4:152324241-152324241 - 587222 COSM1206905 c.555G>T p.K185N Substitution - Missense 4:152350071-152350071 - 2083394 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-HF-7132-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - XHDG17C COSM27052 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - 1206695 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T2991 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 345 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2083375 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 189 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-DS-A0VN-01 COSM460671 c.1557T>A p.Y519* Substitution - Nonsense 4:152326093-152326093 - S02243 COSM5677867 c.1321C>G p.R441G Substitution - Missense 4:152328305-152328305 - 10606 COSM5751536 c.1393_1394insC p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - TCGA-GN-A262-06 COSM3600916 c.1498C>T p.H500Y Substitution - Missense 4:152326152-152326152 - pfg068T COSM4762869 c.854C>A p.P285H Substitution - Missense 4:152337809-152337809 - ICGC_MB518 COSM306984 c.726+1G>A p.? Unknown 4:152346929-152346929 - TCGA-18-5595-01 COSM732380 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - ICGC_MB74 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 6604 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - RPMI COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2071384 COSM33844 c.? p.R505C Substitution - Missense 1044490 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - CR007 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2159468 COSM96316 c.1267G>A p.G423R Substitution - Missense 4:152328359-152328359 - TCGA-AA-3560-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - WC00125 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-D1-A16I-01 COSM1052092 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - TL28 COSM5751739 c.1061C>CT p.Y355fs*8 Complex - frameshift 4:152330793-152330793 - OSCC-GB_01300111 COSM5895336 c.585-5delT p.? Unknown 4:152347076-152347076 - B106 COSM1753571 c.1590T>G p.T530T Substitution - coding silent 4:152326060-152326060 - 587398 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T2647 COSM1052102 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - 2467887 COSM5031087 c.? p.? Unknown ESCC-059T COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 2492723 COSM5723743 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - TCGA-E2-A15L-01 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - TCGA-BS-A0UA-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2321318 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - OSCC-GB_01310111 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 15 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - ESO-147 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 424 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD4002a COSM161026 c.1322G>T p.R441L Substitution - Missense 4:152328304-152328304 - TCGA-18-4083-01 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - E11 COSM1666566 c.585-4delG p.? Unknown 4:152347075-152347075 - 1247754 COSM33843 c.? p.R465C Substitution - Missense TCGA-EE-A29D-06 COSM3600921 c.1267G>T p.G423* Substitution - Nonsense 4:152328359-152328359 - TCGA-FV-A4ZQ-01 COSM4921972 c.892C>A p.P298T Substitution - Missense 4:152332689-152332689 - LUAD-E01317 COSM403808 c.1391T>A p.V464E Substitution - Missense 4:152328235-152328235 - 2083418 COSM256125 c.1202_1204delACA p.N401del Deletion - In frame 4:152329704-152329706 - P12-ICHIKAWA COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BR-8678-01 COSM4122768 c.1210A>G p.K404E Substitution - Missense 4:152329698-152329698 - ESCC_6 COSM4762877 c.115G>T p.E39* Substitution - Nonsense 4:152411689-152411689 - 2432693 COSM28490 c.? p.? Unknown T2769 COSM4745533 c.1335_1336GT>TG p.W446G Substitution - Missense 4:152328290-152328291 - PD5725a COSM4385611 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - sysucc-274T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - AOCS-116-1-3 COSM4138069 c.868C>G p.L290V Substitution - Missense 4:152332713-152332713 - TCGA-85-6561-01 COSM732377 c.1435C>A p.R479R Substitution - coding silent 4:152326215-152326215 - TCGA-CG-4305-01 COSM4122754 c.1677T>C p.L559L Substitution - coding silent 4:152324362-152324362 - PD6086a COSM4383977 c.1859C>T p.P620L Substitution - Missense 4:152323146-152323146 - 1044501 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 307 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-G4-6309-01 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - HCC2998 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 1115501 COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - 1044488 COSM22978 c.658C>T p.Q220* Substitution - Nonsense 4:152346998-152346998 - TCGA-AG-3594-01 COSM256125 c.1202_1204delACA p.N401del Deletion - In frame 4:152329704-152329706 - RPMI-8402 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1115206 COSM27054 c.1556A>G p.Y519C Substitution - Missense 4:152326094-152326094 - TCGA-DK-A1AC-01 COSM1309807 c.1637C>T p.S546L Substitution - Missense 4:152326013-152326013 - 185T COSM4381110 c.726+2delT p.? Unknown 4:152346928-152346928 - D21 COSM5007909 c.1329delC p.V445fs*53 Deletion - Frameshift 4:152328297-152328297 - CRC-10T COSM5457709 c.584+1G>T p.? Unknown 4:152350041-152350041 - I2L-P24Ta-Tumor-Organoid COSM5355755 c.501delA p.M168fs*1 Deletion - Frameshift 4:152411303-152411303 - AOCS-116-1-3 COSM4138068 c.868C>G p.L290V Substitution - Missense 4:152332713-152332713 - PD6187a COSM4385612 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - SJTALL003 COSM305953 c.1411G>T p.E471* Substitution - Nonsense 4:152328215-152328215 - TCGA-CM-4750-01 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - DM10 COSM5608723 c.1690C>A p.R564S Substitution - Missense 4:152324349-152324349 - 1499696 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-CM-4744-01 COSM1427786 c.1259_1260insGTGGGACA p.H420fs*13 Insertion - Frameshift 4:152328366-152328367 - TCGA-D5-6931-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-B5-A0JV-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 526T COSM306982 c.726+1G>A p.? Unknown 4:152346929-152346929 - YUKAT COSM3127900 c.2019G>A p.W673* Substitution - Nonsense 4:152322986-152322986 - TCGA-AP-A05A-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 407 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - LoVo COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1499693 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - TLE48 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10-54 COSM1645395 c.1812A>C p.K604N Substitution - Missense 4:152324227-152324227 - T12 COSM5344633 c.1931G>A p.G644E Substitution - Missense 4:152323074-152323074 - 1813486 COSM33842 c.? p.R465H Substitution - Missense ICC014T COSM5823615 c.333G>T p.E111D Substitution - Missense 4:152411471-152411471 - 1988996 COSM1651752 c.563G>T p.C188F Substitution - Missense 4:152350063-152350063 - ESCC_BICR_061T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - T162 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2467897 COSM1052091 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - TCGA-A6-6137-01 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - YULAN COSM1695085 c.1118C>T p.P373L Substitution - Missense 4:152330736-152330736 - TCGA-F5-6814-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - SKOV3 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - TLE36 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1247759 COSM33845 c.? p.R479Q Substitution - Missense KARPAS45 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - CHC301T COSM3669250 c.1102G>C p.G368R Substitution - Missense 4:152330752-152330752 - 07-057 COSM3736337 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - TCGA-AG-3892-01 COSM206731 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 1043429 COSM22990 c.361_363GAG>TAT p.E121Y Substitution - Missense 4:152411441-152411443 - TLE84 COSM4167995 c.1578G>A p.W526* Substitution - Nonsense 4:152326072-152326072 - 2201852 COSM3738522 c.103C>T p.R35C Substitution - Missense 4:152411701-152411701 - 2467902 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - MOLT-13 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - AML_535 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1044507 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 587284 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T1743 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 2334191 COSM320385 c.1847C>T p.T616I Substitution - Missense 4:152324192-152324192 - 399 COSM4429268 c.1587G>A p.E529E Substitution - coding silent 4:152326063-152326063 - pfg068T COSM4762870 c.854C>A p.P285H Substitution - Missense 4:152337809-152337809 - T-LBL-39 COSM33843 c.? p.R465C Substitution - Missense 1738943 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - sysucc-771T COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - P6 COSM133117 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - MEL-JWCI-14 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ICGC_MB78 COSM3765113 c.2060G>A p.G687E Substitution - Missense 4:152322945-152322945 - TCGA-E6-A1LZ-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - pfg016T COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - D21 COSM5007903 c.1794_1795insA p.A599fs*6 Insertion - Frameshift 4:152324244-152324245 - 1738938 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - HCC2998 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - T-LBL-56 COSM5885258 c.? p.Y519D Substitution - Missense CCRF-CEM COSM327077 c.2054C>T p.A685V Substitution - Missense 4:152322951-152322951 - TCGA-04-1337-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - sysucc-627T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AP-A0LM-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - HN243PT COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-G4-6293-01 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - B22 COSM300416 c.1558G>A p.D520N Substitution - Missense 4:152326092-152326092 - Gp2D COSM1427728 c.1395T>C p.R465R Substitution - coding silent 4:152328231-152328231 - DM79 COSM5608736 c.1792A>C p.N598H Substitution - Missense 4:152324247-152324247 - LC163 COSM5369827 c.1519G>A p.V507I Substitution - Missense 4:152326131-152326131 - 1644a COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 166 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-EO-A1Y5-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1556217 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 234 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - D6 COSM5007225 c.2000G>T p.G667V Substitution - Missense 4:152323005-152323005 - TCGA-BK-A13C-01 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TLE83 COSM4168001 c.1390G>A p.V464M Substitution - Missense 4:152328236-152328236 - 1115323 COSM27056 c.32A>G p.K11R Substitution - Missense 4:152411772-152411772 - 10059 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2321345 COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - TCGA-FV-A4ZQ-01 COSM4921971 c.892C>A p.P298T Substitution - Missense 4:152332689-152332689 - 2071403 COSM33845 c.? p.R479Q Substitution - Missense T2583 COSM4122774 c.1072C>T p.Q358* Substitution - Nonsense 4:152330782-152330782 - TCGA-D1-A160-01 COSM1052146 c.386A>C p.D129A Substitution - Missense 4:152411418-152411418 - TCGA-C5-A1ML-01 COSM4837612 c.1972C>A p.R658R Substitution - coding silent 4:152323033-152323033 - S09-31237-TP COSM4992102 c.555G>A p.K185K Substitution - coding silent 4:152350071-152350071 - 2157499 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2138894 COSM306982 c.726+1G>A p.? Unknown 4:152346929-152346929 - 6975 COSM5751365 c.1554_1555insC p.Y519fs*2 Insertion - Frameshift 4:152326095-152326096 - 394 COSM3721800 c.1631T>A p.V544D Substitution - Missense 4:152326019-152326019 - sysucc-1972T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-HU-A4GN-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ICGC_MB78 COSM3765114 c.2060G>A p.G687E Substitution - Missense 4:152322945-152322945 - 1118428 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - sysucc-809T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1206639 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD2746a COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CCRF-CEM COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - sysucc-771T COSM327079 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - MM19T COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - CCRF-CEM COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1738964 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - 60T COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PCSI_0090_Pa_P COSM3380837 c.778T>C p.C260R Substitution - Missense 4:152337885-152337885 - 10-428 COSM1645199 c.1057delA p.S353fs*24 Deletion - Frameshift 4:152330797-152330797 - TCGA-A6-2677-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-BR-8372-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 900T COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 09-882 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-EF-5830-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - sysucc-1972T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - SJTALL003 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PT23_2 COSM5895336 c.585-5delT p.? Unknown 4:152347076-152347076 - TCGA-BR-8678-01 COSM4122769 c.1210A>G p.K404E Substitution - Missense 4:152329698-152329698 - ESCC_130 COSM1052139 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - PD6171a COSM4385612 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - P12ichikawa COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PDA_105 COSM5003732 c.1786T>G p.S596A Substitution - Missense 4:152324253-152324253 - 2071411 COSM1732673 c.? p.R479G Substitution - Missense 1044503 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD11163a COSM5945089 c.1262C>T p.T421I Substitution - Missense 4:152328364-152328364 - 2083386 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2467885 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 368 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1044508 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - C113 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - ICGC_MB61 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-EE-A2M6-06 COSM3600942 c.545C>T p.S182F Substitution - Missense 4:152350081-152350081 - 2321302 COSM4774924 c.1393C>A p.R465S Substitution - Missense 4:152328233-152328233 - 1813488 COSM33842 c.? p.R465H Substitution - Missense TCGA-BR-A4QL-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1500572 COSM87016 c.? p.W486* Substitution - Nonsense TLE48 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 2542211 COSM166364 c.? p.R658* Substitution - Nonsense 4760_PT COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 1988976 COSM1651753 c.338_342delAGGAG p.E113fs*9 Deletion - Frameshift 4:152411462-152411466 - ESCC_BICR_045T COSM123128 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - TCGA-FU-A2QG-01 COSM4849071 c.1498C>G p.H500D Substitution - Missense 4:152326152-152326152 - CRC-7 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 1116971 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1115203 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - D13 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 2492712 COSM5606546 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - NYU939 COSM4770751 c.1431_1452del22 p.S478fs*13 Deletion - Frameshift 4:152326198-152326219 - 407 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - sysucc-912T COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T3082 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 166 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - WT026 COSM33763 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - TCGA-66-2744-01 COSM732373 c.1368C>A p.T456T Substitution - coding silent 4:152328258-152328258 - ICGC_MB78 COSM3765118 c.1834C>T p.Q612* Substitution - Nonsense 4:152324205-152324205 - SJHGG109_A COSM4971903 c.780T>A p.C260* Substitution - Nonsense 4:152337883-152337883 - 2471674 COSM33842 c.? p.R465H Substitution - Missense 2217109 COSM4169407 c.? p.R35C Substitution - Missense VACO10 COSM133117 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - TCGA-GF-A3OT-06 COSM3600945 c.358C>T p.Q120* Substitution - Nonsense 4:152411446-152411446 - 363 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ICGC_MB61 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - Gp5D COSM3127940 c.1739A>G p.H580R Substitution - Missense 4:152324300-152324300 - TCGA-BT-A20O-01 COSM420169 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - 522_T COSM3127946 c.1735G>T p.G579W Substitution - Missense 4:152324304-152324304 - BD246T COSM732384 c.1550G>A p.G517E Substitution - Missense 4:152326100-152326100 - 1735515 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1043430 COSM22963 c.1110_1111insTC p.K371fs*7 Insertion - Frameshift 4:152330743-152330744 - SJTALL003 COSM305937 c.1412A>G p.E471G Substitution - Missense 4:152328214-152328214 - T36 COSM3127926 c.1877C>T p.A626V Substitution - Missense 4:152323128-152323128 - DM1 COSM5608718 c.1675C>T p.L559F Substitution - Missense 4:152324364-152324364 - T-LBL-93 COSM33842 c.? p.R465H Substitution - Missense TCGA-AX-A0J0-01 COSM1052118 c.958C>A p.L320I Substitution - Missense 4:152332623-152332623 - TCGA-EE-A29E-06 COSM3600932 c.893C>T p.P298L Substitution - Missense 4:152332688-152332688 - T3011 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - SJTALL200 COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-AP-A051-01 COSM1052129 c.739C>A p.P247T Substitution - Missense 4:152337924-152337924 - 587376 COSM1052136 c.671G>A p.R224Q Substitution - Missense 4:152346985-152346985 - 1244724 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1179 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - RMS222 COSM5881197 c.1574T>C p.V525A Substitution - Missense 4:152326076-152326076 - 2083401 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1117026 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1206650 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-BR-6852-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AX-A0J0-01 COSM1052117 c.958C>A p.L320I Substitution - Missense 4:152332623-152332623 - TCGA-AX-A05Z-01 COSM1052144 c.403G>T p.D135Y Substitution - Missense 4:152411401-152411401 - 24T COSM3714715 c.2077G>A p.E693K Substitution - Missense 4:152322928-152322928 - 2011-2343:2012-334-T COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - TBR05 COSM4168005 c.1310G>T p.G437V Substitution - Missense 4:152328316-152328316 - 1738968 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - SUM149PT COSM22996 c.1644_1645ins416 p.F549fs*6 Insertion - Frameshift TL76 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - P105 COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - HN_62376 COSM123128 c.1627A>G p.R543G Substitution - Missense 4:152326023-152326023 - PA086 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SNU-175 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D1-A16I-01 COSM1052122 c.802_803delAT p.M268fs*18 Deletion - Frameshift 4:152337860-152337861 - CTV1 COSM327079 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - MDAH2774 COSM25018 c.862-1G>A p.? Unknown 4:152332720-152332720 - 2159515 COSM3734995 c.? p.K299fs*? Unknown TCGA-AX-A0IU-01 COSM1052113 c.985+1delG p.? Unknown 4:152332595-152332595 - TCGA-A6-3807-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1044511 COSM22988 c.1628G>A p.R543K Substitution - Missense 4:152326022-152326022 - TCGA-DG-A2KK-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1044741 COSM22936 c.2077G>A p.E693K Substitution - Missense 4:152322928-152322928 - T3454 COSM4684124 c.1347_1348delGA p.E449fs*22 Deletion - Frameshift 4:152328278-152328279 - 2321343 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ESCC_131 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - RMS2111 COSM5677866 c.1321C>G p.R441G Substitution - Missense 4:152328305-152328305 - CHC327T COSM4957966 c.1272A>G p.V424V Substitution - coding silent 4:152328354-152328354 - 2467904 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJTALL003 COSM305951 c.1411G>T p.E471* Substitution - Nonsense 4:152328215-152328215 - TL31 COSM5751237 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - YUWHIM COSM1695081 c.1499A>G p.H500R Substitution - Missense 4:152326151-152326151 - 1302184 COSM22937 c.349_351delGAG p.E117del Deletion - In frame 4:152411453-152411455 - 1813472 COSM1155756 c.? p.W446* Substitution - Nonsense SK-OV-3 COSM99657 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - 2334191 COSM320383 c.1847C>T p.T616I Substitution - Missense 4:152324192-152324192 - ICGC_MB78 COSM3765118 c.1834C>T p.Q612* Substitution - Nonsense 4:152324205-152324205 - S10-24679-TP COSM4992097 c.1492A>T p.M498L Substitution - Missense 4:152326158-152326158 - 2071394 COSM33845 c.? p.R479Q Substitution - Missense 1738961 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - 587322 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - T80 COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - ESCC-F75 COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - pfg181T COSM22964 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - BD49T COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - HT115 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-HT-A618-01 COSM4420619 c.2020C>T p.R674W Substitution - Missense 4:152322985-152322985 - 381LT COSM4381199 c.285delA p.E96fs*73 Deletion - Frameshift 4:152411519-152411519 - TCGA-A1-A0SP-01 COSM1485747 c.925delC p.R309fs*33 Deletion - Frameshift 4:152332656-152332656 - TLE43 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - U1 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T3038 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-GM-A3XL-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-22-1012-01 COSM732396 c.1963G>T p.E655* Substitution - Nonsense 4:152323042-152323042 - 1813478 COSM33843 c.? p.R465C Substitution - Missense 2432697 COSM28490 c.? p.? Unknown 1738967 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - P6 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - C135 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - TCGA-BK-A0C9-01 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-BR-6852-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AA-A01Z-01 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - T-LBL-15 COSM5885254 c.? p.R465Y Substitution - Missense RPMI-8402 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 345 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 4624/93P COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-FU-A57G-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 09-842 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T3011 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-AG-3892-01 COSM206732 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 1813482 COSM33842 c.? p.R465H Substitution - Missense TCGA-AK-3447-01 COSM1495746 c.486T>A p.Y162* Substitution - Nonsense 4:152411318-152411318 - DM79 COSM5608737 c.1792A>C p.N598H Substitution - Missense 4:152324247-152324247 - 10606 COSM5751537 c.1393_1394insC p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1244708 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1114865 COSM27052 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - TCGA-BT-A20O-01 COSM420170 c.1436G>C p.R479P Substitution - Missense 4:152326214-152326214 - TCGA-EE-A2MT-06 COSM3600926 c.1103G>A p.G368E Substitution - Missense 4:152330751-152330751 - 07-057 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - 10-115 COSM1427791 c.1259A>G p.H420R Substitution - Missense 4:152328367-152328367 - 2157488 COSM27058 c.1436G>T p.R479L Substitution - Missense 4:152326214-152326214 - PD11053a COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T-ALL16 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-FU-A5XV-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - P12-ICHIKAWA COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 10-671 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BR-8372-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - PD6944a COSM4383981 c.667C>T p.R223C Substitution - Missense 4:152346989-152346989 - 2521260 COSM5895337 c.585-5delT p.? Unknown 4:152347076-152347076 - T-LBL-80 COSM5885256 c.? p.W486C Substitution - Missense 2492713 COSM5606547 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - 1N56-VS-1T56 COSM4977244 c.1359T>A p.C453* Substitution - Nonsense 4:152328267-152328267 - 2492722 COSM5723744 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - ESO-147 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - sysucc-1397T COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10-428 COSM1645198 c.1057delA p.S353fs*24 Deletion - Frameshift 4:152330797-152330797 - 1500573 COSM87017 c.? p.V265I Substitution - Missense LUAD-E01317 COSM403809 c.1391T>A p.V464E Substitution - Missense 4:152328235-152328235 - TCGA-D1-A103-01 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - T1743 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1219465 COSM30597 c.892C>T p.P298S Substitution - Missense 4:152332689-152332689 - T162 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - sysucc-771T COSM327081 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - 1738963 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - 1219462 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - TCGA-FU-A2QG-01 COSM4849070 c.1498C>G p.H500D Substitution - Missense 4:152326152-152326152 - TCGA-BS-A0UA-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - E9 COSM1666337 c.1112A>C p.K371T Substitution - Missense 4:152330742-152330742 - 27 COSM5748786 c.1319A>T p.D440V Substitution - Missense 4:152328307-152328307 - 8067521 COSM1427763 c.1313C>A p.S438Y Substitution - Missense 4:152328313-152328313 - PD6217a COSM4385611 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - TCGA-BR-8680-01 COSM206731 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 1044491 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 587302 COSM1206892 c.1625A>T p.N542I Substitution - Missense 4:152326025-152326025 - HN243PT COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-A5-A0GP-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HCA7 COSM206699 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - S10-24679-TP COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - Au8 COSM5606546 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - TCGA-GN-A262-06 COSM3600917 c.1498C>T p.H500Y Substitution - Missense 4:152326152-152326152 - TCGA-AA-3713-01 COSM1427641 c.1877C>A p.A626D Substitution - Missense 4:152323128-152323128 - 366TS COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AH-6903-01 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - 1115548 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 17205/93C COSM22976 c.1514G>C p.R505P Substitution - Missense 4:152326136-152326136 - TCGA-EE-A29E-06 COSM3600931 c.893C>T p.P298L Substitution - Missense 4:152332688-152332688 - TCGA-AP-A05J-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2379659 COSM5031087 c.? p.? Unknown TCGA-ER-A19F-06 COSM3600937 c.721T>C p.F241L Substitution - Missense 4:152346935-152346935 - TCGA-18-3406-01 COSM732387 c.1754G>C p.S585T Substitution - Missense 4:152324285-152324285 - CHC327T COSM4957965 c.1272A>G p.V424V Substitution - coding silent 4:152328354-152328354 - 180 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - PD13773a COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2532137 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TLE43 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - OSCC-GB_00240111 COSM3714715 c.2077G>A p.E693K Substitution - Missense 4:152322928-152322928 - 1813481 COSM33843 c.? p.R465C Substitution - Missense ICGC_MB61 COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TCGA-CG-5733-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ATL1 COSM28798 c.1258C>T p.H420Y Substitution - Missense 4:152328368-152328368 - 1044495 COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - 1116984 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 9835 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1116997 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - GB23 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TLE48 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-EA-A3QE-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - sysucc-882T COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - CRC-09T COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - TL76 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - SM54 COSM166366 c.? p.T576fs*29 Unknown 60T COSM110667 c.1777_1778insT p.L594fs*11 Insertion - Frameshift 4:152324261-152324262 - 1738941 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - 2521243 COSM5886335 c.295G>A p.E99K Substitution - Missense 4:152411509-152411509 - TCGA-AN-A046-01 COSM3825380 c.257C>T p.S86L Substitution - Missense 4:152411547-152411547 - SNU-C2B COSM3127945 c.1735G>T p.G579W Substitution - Missense 4:152324304-152324304 - 452/94C COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - SC_9008 COSM1309808 c.1637C>T p.S546L Substitution - Missense 4:152326013-152326013 - T407 COSM4684103 c.1817G>A p.W606* Substitution - Nonsense 4:152324222-152324222 - 2083382 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-AX-A1C7-01 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - 1044736 COSM22931 c.1318G>A p.D440N Substitution - Missense 4:152328308-152328308 - LUAD-D02326 COSM393140 c.1095G>A p.W365* Substitution - Nonsense 4:152330759-152330759 - TCGA-CA-6717-01 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1206656 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1044512 COSM22989 c.1634A>G p.Y545C Substitution - Missense 4:152326016-152326016 - TCGA-DC-6682-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 166 COSM99604 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-BH-A2L8-01 COSM3825361 c.1195G>C p.D399H Substitution - Missense 4:152329713-152329713 - ESCC_118 COSM4762865 c.1275G>A p.W425* Substitution - Nonsense 4:152328351-152328351 - 2521259 COSM5895336 c.585-5delT p.? Unknown 4:152347076-152347076 - PD2752a COSM27916 c.? p.? Unknown 4:152329671-152329671 - T3502 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - PCSI_0103_Pa_P COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-CG-5721-01 COSM4122763 c.1442C>T p.A481V Substitution - Missense 4:152326208-152326208 - TCGA-CA-6717-01 COSM206731 c.41G>A p.R14Q Substitution - Missense 4:152411763-152411763 - 587254 COSM1206878 c.664C>T p.R222* Substitution - Nonsense 4:152346992-152346992 - Pat_26_A COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - 2492720 COSM5723743 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - 2083384 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-EI-6917-01 COSM22972 c.845C>A p.S282* Substitution - Nonsense 4:152337818-152337818 - TCGA-14-0817 COSM167199 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 1115204 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1043432 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 299 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-A5-A0R8-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T3306 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-F4-6703-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 804-02-4TD COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3033 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2521243 COSM5886336 c.295G>A p.E99K Substitution - Missense 4:152411509-152411509 - 2379662 COSM5031087 c.? p.? Unknown B110 COSM1753582 c.873T>A p.Y291* Substitution - Nonsense 4:152332708-152332708 - TCGA-CU-A0YR-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - 2321355 COSM3600937 c.721T>C p.F241L Substitution - Missense 4:152346935-152346935 - BD114T COSM5502910 c.1320delT p.R441fs*57 Deletion - Frameshift 4:152328306-152328306 - 1044496 COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - TCGA-24-1565-01 COSM78946 c.1952T>A p.L651* Substitution - Nonsense 4:152323053-152323053 - 1247756 COSM33844 c.? p.R505C Substitution - Missense 101213 COSM96318 c.668G>T p.R223L Substitution - Missense 4:152346988-152346988 - P13 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 587376 COSM1052109 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - B89-10-Tumor COSM1753577 c.1311A>T p.G437G Substitution - coding silent 4:152328315-152328315 - PD9571a COSM5752725 c.145G>T p.E49* Substitution - Nonsense 4:152411659-152411659 - 1992410 COSM33842 c.? p.R465H Substitution - Missense T-LBL-102 COSM235639 c.? p.R465L Substitution - Missense pfg127T COSM4762859 c.1508C>T p.A503V Substitution - Missense 4:152326142-152326142 - E11 COSM1666565 c.585-4delG p.? Unknown 4:152347075-152347075 - ESCC-F18 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1219475 COSM25812 c.1514G>A p.R505H Substitution - Missense 4:152326136-152326136 - TCGA-GN-A262-06 COSM3600912 c.1632C>G p.V544V Substitution - coding silent 4:152326018-152326018 - PD9324a COSM1052091 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - TCGA-AX-A0IU-01 COSM1052114 c.985+1delG p.? Unknown 4:152332595-152332595 - 1813469 COSM1155763 c.? p.I434fs*3 Deletion - Frameshift 2083391 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-A5-A0VP-01 COSM1052151 c.40C>T p.R14* Substitution - Nonsense 4:152411764-152411764 - PCSI_0269_Pa_P_526 COSM4961914 c.1690C>T p.R564C Substitution - Missense 4:152324349-152324349 - TCGA-AF-2687-01 COSM206697 c.1435C>T p.R479* Substitution - Nonsense 4:152326215-152326215 - 2321333 COSM4775044 c.1265G>T p.G422V Substitution - Missense 4:152328361-152328361 - 10211 COSM5751206 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - TCGA-A2-A0D0-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1244723 COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - 1524379 COSM96473 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - TCGA-FI-A2EX-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1499695 COSM86992 c.1792A>G p.N598D Substitution - Missense 4:152324247-152324247 - CCRF-CEM COSM327075 c.2054C>T p.A685V Substitution - Missense 4:152322951-152322951 - TCGA-AA-3837-01 COSM271648 c.860A>T p.E287V Substitution - Missense 4:152337803-152337803 - 1N56-VS-1T56 COSM4977243 c.1359T>A p.C453* Substitution - Nonsense 4:152328267-152328267 - 2432709 COSM28490 c.? p.? Unknown 399 COSM4429269 c.1587G>A p.E529E Substitution - coding silent 4:152326063-152326063 - PD4845a COSM5781537 c.830A>C p.Q277P Substitution - Missense 4:152337833-152337833 - TCGA-AX-A0J0-01 COSM206685 c.1973G>A p.R658Q Substitution - Missense 4:152323032-152323032 - BD246T COSM732383 c.1550G>A p.G517E Substitution - Missense 4:152326100-152326100 - 1044510 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - LUAD-D02326 COSM393141 c.1095G>A p.W365* Substitution - Nonsense 4:152330759-152330759 - ICGC_MB61 COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - PGBM14 COSM510744 c.566_567delAA p.K189fs*66 Deletion - Frameshift 4:152350059-152350060 - TL26 COSM5751729 c.664C>CT p.R222fs*34 Complex - frameshift 4:152346992-152346992 - 1813485 COSM33842 c.? p.R465H Substitution - Missense I2L-P24Ta-Tumor-Biopsy COSM5355754 c.501delA p.M168fs*1 Deletion - Frameshift 4:152411303-152411303 - TCGA-EW-A1PE-01 COSM1485742 c.1070G>A p.R357K Substitution - Missense 4:152330784-152330784 - T3498 COSM22968 c.1417_1418insA p.R473fs*4 Insertion - Frameshift 4:152328208-152328209 - 6975 COSM5751359 c.2065C>CT p.R689fs*5 Complex - frameshift 4:152322940-152322940 - TCGA-25-1316-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 109T COSM5575929 c.658C>T p.Q220* Substitution - Nonsense 4:152346998-152346998 - 2321355 COSM4775178 c.2039_2040delCA p.T680fs*13 Deletion - Frameshift 4:152322965-152322966 - T2583 COSM4122773 c.1072C>T p.Q358* Substitution - Nonsense 4:152330782-152330782 - 2492723 COSM5723744 c.1122G>A p.K374K Substitution - coding silent 4:152330732-152330732 - TCGA-60-2698-01 COSM732400 c.2033C>G p.S678* Substitution - Nonsense 4:152322972-152322972 - HSB2 COSM327079 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - 47 COSM5734337 c.1133_1147del15 p.G378_H382delGHDDH Deletion - In frame 4:152329761-152329775 - sysucc-627T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2138885 COSM33844 c.? p.R505C Substitution - Missense TCGA-FS-A1YY-06 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 60T COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1115502 COSM27059 c.1451G>C p.R484T Substitution - Missense 4:152326199-152326199 - 1044738 COSM22933 c.1947G>A p.W649* Substitution - Nonsense 4:152323058-152323058 - TCGA-BR-8360-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 9583_CLM COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - 2011-2260:2012-1319-T COSM4604317 c.1394G>C p.R465P Substitution - Missense 4:152328232-152328232 - 2321355 COSM4775179 c.2039_2040delCA p.T680fs*13 Deletion - Frameshift 4:152322965-152322966 - TL45 COSM5751891 c.2065_2066insA p.R689fs*5 Insertion - Frameshift 4:152322939-152322940 - 09-842 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - KARPAS-45 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AP-A05H-01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1115413 COSM27061 c.45_46insCCT p.T15_G16insP Insertion - In frame 4:152411758-152411759 - TCGA-A6-5661-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1N25-VS-1T25 COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - TCGA-D1-A103-01 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-CM-4750-01 COSM5157012 c.109_115delGTAGAGG p.V37fs*24 Deletion - Frameshift 4:152411689-152411695 - T3049 COSM4684134 c.1202A>G p.N401S Substitution - Missense 4:152329706-152329706 - TCGA-BR-4256-01 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1499691 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 10-555 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ZZUFHECRKL-G067T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - HN137PT COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - TCGA-D5-6928-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D1-A16Y-01 COSM206733 c.37C>T p.R13* Substitution - Nonsense 4:152411767-152411767 - 587222 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - XHDG53C COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1813496 COSM1155758 c.? p.R479S Substitution - Missense 2389322 COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - WT026 COSM732380 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 037 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2083393 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1874632 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10-76 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1043934 COSM22937 c.349_351delGAG p.E117del Deletion - In frame 4:152411453-152411455 - T36 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 2011-2343:2012-334-T COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - PCSI_0090_Pa_X COSM3380836 c.778T>C p.C260R Substitution - Missense 4:152337885-152337885 - RK150_C01 COSM3767732 c.1438G>A p.D480N Substitution - Missense 4:152326212-152326212 - 1116944 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1738966 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - P6 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - T3 COSM732380 c.1513C>A p.R505S Substitution - Missense 4:152326137-152326137 - 2467903 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-EA-A3HQ-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 132 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 6948_PT COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-EA-A3HQ-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SJTALL003 COSM305939 c.1540G>T p.V514F Substitution - Missense 4:152326110-152326110 - TCGA-BR-4201-01 COSM4122779 c.584+2T>C p.? Unknown 4:152350040-152350040 - ESCC_38 COSM5629158 c.1780C>T p.L594F Substitution - Missense 4:152324259-152324259 - 1247753 COSM33843 c.? p.R465C Substitution - Missense ESCC_73 COSM5634579 c.1388C>G p.T463S Substitution - Missense 4:152328238-152328238 - 2321333 COSM4775049 c.1436_1437insT p.D480fs*5 Insertion - Frameshift 4:152326213-152326214 - 2467881 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1874643 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - 1247760 COSM33846 c.? p.R479L Substitution - Missense LOVO COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-BS-A0U8-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - HSB2 COSM327081 c.1429G>A p.G477S Substitution - Missense 4:152326221-152326221 - 3988 COSM5751152 c.1268G>GT p.V424fs*13 Complex - frameshift 4:152328358-152328358 - CTV1 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 11490 COSM5751560 c.1014_1018delAAGAA p.R339fs*22 Deletion - Frameshift 4:152330836-152330840 - T3151 COSM4684128 c.1275G>T p.W425C Substitution - Missense 4:152328351-152328351 - SJTALL003 COSM305953 c.1411G>T p.E471* Substitution - Nonsense 4:152328215-152328215 - ME009T COSM222953 c.1802C>T p.S601F Substitution - Missense 4:152324237-152324237 - P8 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-D1-A16I-01 COSM1052091 c.1322G>A p.R441Q Substitution - Missense 4:152328304-152328304 - TCGA-B5-A11E-01 COSM1052149 c.154C>T p.H52Y Substitution - Missense 4:152411650-152411650 - TCGA-C5-A1ML-01 COSM4837611 c.1972C>A p.R658R Substitution - coding silent 4:152323033-152323033 - 587394 COSM167306 c.1798G>T p.D600Y Substitution - Missense 4:152324241-152324241 - 177-01-9TD COSM33762 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - TCGA-AP-A05H-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 587398 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-A8-A09M-01 COSM447500 c.902T>C p.L301P Substitution - Missense 4:152332679-152332679 - SM19 COSM166367 c.? p.S668fs*26 Unknown 1813467 COSM33841 c.? p.G423V Substitution - Missense TCGA-EK-A2RL-01 COSM673925 c.1394G>T p.R465L Substitution - Missense 4:152328232-152328232 - TCGA-D1-A16X-01 COSM302215 c.2066G>A p.R689Q Substitution - Missense 4:152322939-152322939 - 1044737 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 2138889 COSM3718362 c.? p.S282* Substitution - Nonsense TCGA-D1-A101-01 COSM1052095 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-EF-5830-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2321343 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - PACA-44-T COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 10-555 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 2467889 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ESCC_118 COSM4762864 c.1275G>A p.W425* Substitution - Nonsense 4:152328351-152328351 - 1116959 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 587322 COSM22979 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - S0021 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - CRC-7 COSM206683 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - TCGA-AX-A0J0-01 COSM1052125 c.744G>T p.E248D Substitution - Missense 4:152337919-152337919 - PD13773a COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2083419 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - TCGA-21-1078-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-AP-A05J-01 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 11114 COSM5751238 c.1393C>CT p.R465fs*7 Complex - frameshift 4:152328233-152328233 - 6975 COSM5751364 c.1554_1555insC p.Y519fs*2 Insertion - Frameshift 4:152326095-152326096 - PT23_2 COSM5895337 c.585-5delT p.? Unknown 4:152347076-152347076 - 1247750 COSM33843 c.? p.R465C Substitution - Missense 2492712 COSM5606547 c.940T>A p.L314M Substitution - Missense 4:152332641-152332641 - PD2729a COSM22984 c.1268G>T p.G423V Substitution - Missense 4:152328358-152328358 - TCGA-EK-A3GK-01 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - TCGA-F4-6703-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1206638 COSM29551 c.1301_1302ins22 p.I435fs*9 Insertion - Frameshift 4:152328324-152328325 - 1218278 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1206637 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - MM06T COSM4762859 c.1508C>T p.A503V Substitution - Missense 4:152326142-152326142 - TCGA-EE-A2M6-06 COSM3600941 c.545C>T p.S182F Substitution - Missense 4:152350081-152350081 - MM04T COSM34014 c.1321C>T p.R441W Substitution - Missense 4:152328305-152328305 - TCGA-B0-5102-01 COSM480959 c.428T>A p.V143D Substitution - Missense 4:152411376-152411376 - TCGA-DK-A2I2-01 COSM732400 c.2033C>G p.S678* Substitution - Nonsense 4:152322972-152322972 - TCGA-D8-A1XK-01 COSM3825375 c.529G>A p.E177K Substitution - Missense 4:152350097-152350097 - 587400 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - PACA44 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TL19 COSM5751681 c.1136A>AG p.H379fs*2 Complex - frameshift 4:152329772-152329772 - TLE43 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 2467936 COSM5031087 c.? p.? Unknown NYU939 COSM4770750 c.1431_1452del22 p.S478fs*13 Deletion - Frameshift 4:152326198-152326219 - TCGA-B0-5400-01 COSM480952 c.2022G>C p.R674R Substitution - coding silent 4:152322983-152322983 - CCK81 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 10-396 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 262T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 77 COSM206717 c.575A>C p.E192A Substitution - Missense 4:152350051-152350051 - TCGA-AA-3852-01 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2773 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - ESCC_BICR_061T COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 6597 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2083387 COSM305939 c.1540G>T p.V514F Substitution - Missense 4:152326110-152326110 - TCGA-C5-A1M9-01 COSM4830930 c.1798G>A p.D600N Substitution - Missense 4:152324241-152324241 - 47 COSM5734338 c.1133_1147del15 p.G378_H382delGHDDH Deletion - In frame 4:152329761-152329775 - 2138880 COSM33843 c.? p.R465C Substitution - Missense TCGA-D5-6531-01 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TCGA-BR-4256-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1115202 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - SW48 COSM3128082 c.456G>A p.L152L Substitution - coding silent 4:152411348-152411348 - CSCC-60-T COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - 9891 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - LUAD-B01145 COSM333439 c.303T>A p.D101E Substitution - Missense 4:152411501-152411501 - 2467936 COSM1539704 c.1309G>T p.G437* Substitution - Nonsense 4:152328317-152328317 - 09-664 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1500570 COSM87015 c.? p.R278* Substitution - Nonsense ESOSCC156T COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 423 COSM99606 c.1513C>G p.R505G Substitution - Missense 4:152326137-152326137 - T3064 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - TCGA-A1-A0SP-01 COSM1485748 c.925delC p.R309fs*33 Deletion - Frameshift 4:152332656-152332656 - 09-882 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - PA086 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - T3670 COSM320383 c.1847C>T p.T616I Substitution - Missense 4:152324192-152324192 - 587376 COSM1052110 c.1105G>T p.E369* Substitution - Nonsense 4:152330749-152330749 - PD8347a COSM5945084 c.1267G>C p.G423R Substitution - Missense 4:152328359-152328359 - 2071383 COSM33845 c.? p.R479Q Substitution - Missense I2L-P24Ta-Tumor-Organoid COSM5355754 c.501delA p.M168fs*1 Deletion - Frameshift 4:152411303-152411303 - TCGA-AA-3713-01 COSM1427640 c.1877C>A p.A626D Substitution - Missense 4:152323128-152323128 - CP66-MEL COSM22388 c.328G>T p.E110* Substitution - Nonsense 4:152411476-152411476 - TCGA-A8-A0A6-01 COSM3825356 c.1537A>G p.R513G Substitution - Missense 4:152326113-152326113 - 587222 COSM1206904 c.555G>T p.K185N Substitution - Missense 4:152350071-152350071 - 6975 COSM5751360 c.2065C>CT p.R689fs*5 Complex - frameshift 4:152322940-152322940 - 1738936 COSM27052 c.1379A>G p.H460R Substitution - Missense 4:152328247-152328247 - T3064 COSM34018 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - T-LBL-19 COSM5885257 c.? p.A503V Substitution - Missense 07-058 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - 46M COSM5587806 c.2009G>A p.G670E Substitution - Missense 4:152322996-152322996 - TCGA-A2-A3XT-01 COSM3825372 c.529G>C p.E177Q Substitution - Missense 4:152350097-152350097 - DU528 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1219471 COSM30599 c.1576T>C p.W526R Substitution - Missense 4:152326074-152326074 - PACA46 COSM1158148 c.1338G>T p.W446C Substitution - Missense 4:152328288-152328288 - TCGA-BR-4201-01 COSM4122780 c.584+2T>C p.? Unknown 4:152350040-152350040 - BD221T COSM5490559 c.1598G>T p.C533F Substitution - Missense 4:152326052-152326052 - T-LBL-19 COSM33845 c.? p.R479Q Substitution - Missense 1813480 COSM33843 c.? p.R465C Substitution - Missense 205881 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - B-ALL1 COSM28799 c.1409A>C p.H470P Substitution - Missense 4:152328217-152328217 - TCGA-A2-A3XT-01 COSM3825371 c.529G>C p.E177Q Substitution - Missense 4:152350097-152350097 - S02290 COSM5686715 c.1514G>C p.R505P Substitution - Missense 4:152326136-152326136 - 1247763 COSM33841 c.? p.G423V Substitution - Missense T-LBL-56 COSM5885253 c.? p.T463A Substitution - Missense T11 COSM5344638 c.1496G>T p.G499V Substitution - Missense 4:152326154-152326154 - U11T COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - CCRF-CEM COSM327077 c.2054C>T p.A685V Substitution - Missense 4:152322951-152322951 - HN137PT COSM99657 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - 587348 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - P105 COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - 4760_PT COSM327088 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - Gp2D COSM3127941 c.1739A>G p.H580R Substitution - Missense 4:152324300-152324300 - 2138887 COSM33843 c.? p.R465C Substitution - Missense 1247751 COSM33843 c.? p.R465C Substitution - Missense TCGA-JW-A5VJ-01 COSM4818413 c.1522C>T p.Q508* Substitution - Nonsense 4:152326128-152326128 - 3_RESISTANT COSM1723801 c.979delG p.E327fs*15 Deletion - Frameshift 4:152332602-152332602 - 431 COSM1309813 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - MM16T COSM5415242 c.?_?insT p.?fs*? Unknown SJTALL044 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1044505 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - S0021 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - Gp5D COSM1427729 c.1395T>C p.R465R Substitution - coding silent 4:152328231-152328231 - 1350 COSM22973 c.1177C>T p.R393* Substitution - Nonsense 4:152329731-152329731 - 16835 COSM48375 c.1136A>G p.H379R Substitution - Missense 4:152329772-152329772 - KARPAS45 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - sysucc-1465T COSM4604553 c.1817G>T p.W606L Substitution - Missense 4:152324222-152324222 - PCSI_0269_Pa_P_526 COSM4961915 c.1690C>T p.R564C Substitution - Missense 4:152324349-152324349 - 1738939 COSM1155716 c.1514G>H p.R505? Substitution - Missense 4:152326136-152326136 - LP2000331-DNA_A01 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AY-6196-01 COSM1427646 c.1848A>T p.T616T Substitution - coding silent 4:152324191-152324191 - 185T COSM4385944 c.1333_1334insA p.V445fs*27 Insertion - Frameshift 4:152328292-152328293 - TCGA-BS-A0TC-01 COSM1052126 c.744G>T p.E248D Substitution - Missense 4:152337919-152337919 - ESCC-F20 COSM5047306 c.1220C>A p.S407* Substitution - Nonsense 4:152329688-152329688 - TCGA-Q1-A73O-01 COSM4834125 c.829C>G p.Q277E Substitution - Missense 4:152337834-152337834 - 587322 COSM1206899 c.1679A>G p.D560G Substitution - Missense 4:152324360-152324360 - TCGA-AG-3898-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HCC2998 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - GB23 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - HCC174T COSM3660929 c.1415A>C p.K472T Substitution - Missense 4:152328211-152328211 - 1219473 COSM30601 c.1736_1741delGGCACC p.G579_Q581>E Complex - deletion inframe 4:152324298-152324303 - HCC058T COSM5804072 c.1263A>T p.T421T Substitution - coding silent 4:152328363-152328363 - AML_15 COSM732395 c.1963G>T p.E655* Substitution - Nonsense 4:152323042-152323042 - B-ALL3 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 86590 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - 1118430 COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - SNU-175 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-B5-A11E-01 COSM1052148 c.154C>T p.H52Y Substitution - Missense 4:152411650-152411650 - 2471673 COSM33842 c.? p.R465H Substitution - Missense T36 COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - TL19 COSM5751680 c.1136A>AG p.H379fs*2 Complex - frameshift 4:152329772-152329772 - 2083395 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 431 COSM1309812 c.1154C>A p.T385K Substitution - Missense 4:152329754-152329754 - TCGA-BF-A3DL-01 COSM4904813 c.1117C>T p.P373S Substitution - Missense 4:152330737-152330737 - TCGA-AY-6196-01 COSM1427645 c.1848A>T p.T616T Substitution - coding silent 4:152324191-152324191 - ESCC-F34 COSM3767732 c.1438G>A p.D480N Substitution - Missense 4:152326212-152326212 - 452 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2157494 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - TCGA-DI-A1NN-01 COSM22970 c.670C>T p.R224* Substitution - Nonsense 4:152346986-152346986 - 1813475 COSM33843 c.? p.R465C Substitution - Missense ESCC_73 COSM5634578 c.1388C>G p.T463S Substitution - Missense 4:152328238-152328238 - 2083392 COSM27083 c.2065C>T p.R689W Substitution - Missense 4:152322940-152322940 - WM3862 COSM22987 c.1457G>A p.W486* Substitution - Nonsense 4:152326193-152326193 - PD11379a COSM5752537 c.724C>T p.Q242* Substitution - Nonsense 4:152346932-152346932 - ICGC_MB78 COSM3765119 c.1834C>T p.Q612* Substitution - Nonsense 4:152324205-152324205 - T3147 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1116992 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TCGA-AP-A051-01 COSM1052130 c.739C>A p.P247T Substitution - Missense 4:152337924-152337924 - pfg076T COSM4762876 c.115G>T p.E39* Substitution - Nonsense 4:152411689-152411689 - TL19 COSM5751288 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - TCGA-EK-A2PL-01 COSM22966 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - 09-297 COSM108572 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - TL89 COSM5751205 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - SW837 COSM27271 c.1205_1206insT p.L403fs*34 Insertion - Frameshift 4:152329702-152329703 - T3094 COSM4684091 c.2054C>A p.A685E Substitution - Missense 4:152322951-152322951 - TCGA-AA-3848-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-F1-A448-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 16883 COSM48374 c.1438G>T p.D480Y Substitution - Missense 4:152326212-152326212 - TCGA-B5-A11N-01 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 262T COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 2321318 COSM117310 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - T1 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - P12ichikawa COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 19A COSM24620 c.1417delA p.R473fs*25 Deletion - Frameshift 4:152328209-152328209 - TCGA-HF-7132-01 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - 1191-01-02TD COSM126701 c.1099C>T p.R367* Substitution - Nonsense 4:152330755-152330755 - TCGA-18-3409-01 COSM732369 c.535C>T p.R179C Substitution - Missense 4:152350091-152350091 - 423 COSM1177745 c.1322G>C p.R441P Substitution - Missense 4:152328304-152328304 - 1247749 COSM33843 c.? p.R465C Substitution - Missense 2432694 COSM28490 c.? p.? Unknown 2321333 COSM4775045 c.1265G>T p.G422V Substitution - Missense 4:152328361-152328361 - ICGC_MB78 COSM3765113 c.2060G>A p.G687E Substitution - Missense 4:152322945-152322945 - TL28 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 10175 COSM5751287 c.1393_1394insA p.R465fs*7 Insertion - Frameshift 4:152328232-152328233 - 1044500 COSM22986 c.1338G>A p.W446* Substitution - Nonsense 4:152328288-152328288 - 24T COSM22936 c.2077G>A p.E693K Substitution - Missense 4:152322928-152322928 - T80 COSM1177865 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - 10-115 COSM1427792 c.1259A>G p.H420R Substitution - Missense 4:152328367-152328367 - TCGA-EE-A2MT-06 COSM3600927 c.1103G>A p.G368E Substitution - Missense 4:152330751-152330751 - 9967 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - 1788881 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - MEL-JWCI-14 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - 1117005 COSM23000 c.1514G>T p.R505L Substitution - Missense 4:152326136-152326136 - sysucc-1465T COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-D1-A103-01 COSM22967 c.1972C>T p.R658* Substitution - Nonsense 4:152323033-152323033 - TCGA-AA-3672-01 COSM292754 c.1417delA p.R473fs*25 Deletion - Frameshift 4:152328209-152328209 - PT15_1 COSM5895336 c.585-5delT p.? Unknown 4:152347076-152347076 - PD6266a COSM4385611 c.43_44insCTC p.T15_G16insP Insertion - In frame 4:152411760-152411761 - CRC-09T COSM22971 c.832C>T p.R278* Substitution - Nonsense 4:152337831-152337831 - 2011-2260:2012-1319-T COSM4604318 c.1394G>C p.R465P Substitution - Missense 4:152328232-152328232 - TCGA-A2-A0D0-01 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - HBP-ALL COSM27913 c.1580A>G p.D527G Substitution - Missense 4:152326070-152326070 - TCGA-GM-A3XL-01 COSM22932 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - ME009T COSM222957 c.1685C>T p.S562L Substitution - Missense 4:152324354-152324354 - TCGA-HT-A618-01 COSM4420620 c.2020C>T p.R674W Substitution - Missense 4:152322985-152322985 - 1206647 COSM22965 c.1394G>A p.R465H Substitution - Missense 4:152328232-152328232 - PD2734a COSM22974 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - CTV-1 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ME009 COSM22975 c.1513C>T p.R505C Substitution - Missense 4:152326137-152326137 - ESCC-F114 COSM170727 c.1393C>T p.R465C Substitution - Missense 4:152328233-152328233 - TCGA-BR-4371-01 COSM4122758 c.1635T>G p.Y545* Substitution - Nonsense 4:152326015-152326015 - CSCC-38-T COSM4534715 c.2113G>A p.D705N Substitution - Missense 4:152322892-152322892 - HCC058T COSM5804071 c.1263A>T p.T421T Substitution - coding silent 4:152328363-152328363 - sysucc-834T COSM295018 c.1745C>T p.S582L Substitution - Missense 4:152324294-152324294 - 10211 COSM5751205 c.1435_1436insA p.R479fs*6 Insertion - Frameshift 4:152326214-152326215 - LUAD-S01306 COSM343647 c.1617G>A p.G539G Substitution - coding silent 4:152326033-152326033 - 1N25-VS-1T25 COSM1177864 c.1385C>T p.S462F Substitution - Missense 4:152328241-152328241 - 9891 COSM447498 c.1436G>A p.R479Q Substitution - Missense 4:152326214-152326214 - SW48 COSM1427622 c.2001delG p.S668fs*39 Deletion - Frameshift 4:152323004-152323004 - T-LBL-25 COSM5885250 c.? p.G419* Substitution - Nonsense 205881 COSM3127986 c.1435C>G p.R479G Substitution - Missense 4:152326215-152326215 - TCGA-BS-A0TC-01 COSM1052125 c.744G>T p.E248D Substitution - Missense 4:152337919-152337919 - T80 COSM1177744 c.1322G>C p.R441P Substitution - Missense 4:152328304-152328304 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.561069;Hs.561071;Hs.561072;Hs.561073;Hs.561076;Hs.561077;Hs.561078;Hs.561087;Hs.561089;Hs.561093;Hs.561094;Hs.561095;Hs.561102;Hs.561105;Hs.561108;Hs.561109;Hs.561110;Hs.561111;Hs.561113;Hs.561114;Hs.561115;Hs.561116;Hs.561117;Hs.561119;Hs.561120;Hs.561123;Hs.561129;Hs.561130;Hs.561135;Hs.561144;Hs.561145;Hs.561148;Hs.561149;Hs.561150;Hs.561153;Hs.561160;Hs.561161;Hs.561163;Hs.561174;Hs.561177;Hs.561179;Hs.561180;Hs.561181;Hs.561182;Hs.561183;Hs.561187;Hs.561191;Hs.561195;Hs.561198;Hs.561202;Hs.561203;Hs.561205;Hs.561207;Hs.561208;Hs.561216;Hs.561220;Hs.561223;Hs.561226;Hs.561227;Hs.561232;Hs.561234;Hs.561235;Hs.561236;Hs.561237;Hs.561238;Hs.561239;Hs.561241;Hs.561242;Hs.561243;Hs.561245 4q31.3 606278 2438889|CGAP|BC012159|C/T|coding|Pro109Pro|647|Validated; 2438889|CGAP|BC028090|C/T|coding|Pro204Pro|650|Validated; 2438889|CGAP|BC030983|C/T|coding|Pro206Pro|655|Validated; 2438889|CGAP|BC032452|C/T|coding|Pro203Pro|633|Validated; 2438889|CGAP|BC033102|C/T|coding|Pro205Pro|644|Validated; 2438889|CGAP|BC070353|C/T|coding|Pro204Pro|651|Validated; 2438889|CGAP|BC071725|C/T|coding|Pro210Pro|647|Validated; 2438889|CGAP|BC071804|C/T|coding|Pro206Pro|655|Validated; 2438889|CGAP|BC072392|C/T|coding|Pro205Pro|646|Validated; 2438889|CGAP|BC073762|C/T|coding|Pro212Pro|640|Validated; 2438889|CGAP|BC073769|C/T|coding|Pro206Pro|639|Validated; 2438889|CGAP|BC073770|C/T|coding|Pro206Pro|635|Validated; 2438889|CGAP|BC073786|C/T|coding|Pro203Pro|632|Validated; 2438889|CGAP|BC073787|C/T|coding|Pro204Pro|639|Validated; 2438889|CGAP|BC089414|C/T|coding|Pro202Pro|611|Validated; 2438889|CGAP|BC093098|C/T|coding|Pro205Pro|662|Validated; 2438891|CGAP|BC012159|A/T|non-coding||748|Validated; 2438891|CGAP|BC028090|A/T|non-coding||751|Validated; 2438891|CGAP|BC030983|A/T|non-coding||756|Validated; 2438891|CGAP|BC032452|A/T|non-coding||734|Validated; 2438891|CGAP|BC071725|A/T|non-coding||748|Validated; 2438891|CGAP|BC071804|A/T|non-coding||756|Validated; 2438891|CGAP|BC072392|A/T|non-coding||747|Validated; 2438891|CGAP|BC073762|A/T|non-coding||741|Validated; 2438891|CGAP|BC073769|A/T|non-coding||740|Validated; 2438891|CGAP|BC073770|A/T|non-coding||736|Validated; 2438891|CGAP|BC073787|A/T|non-coding||740|Validated; 2438891|CGAP|BC0 Hs.717054;Hs.717055;Hs.717056;Hs.717057;Hs.717059;Hs.717064;Hs.717065;Hs.717068;Hs.717070;Hs.717073;Hs.717076;Hs.717081 4q31.3 606278

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAC - InFrameDeletion p.V475delV c.1423_1425delGTT 4 153247377 HNSC A C Missense p.I85S c.254T>G 4 153332702 BRCA A C Missense p.S516R c.1548T>G 4 153247254 CM A C Nonsense p.Y545* c.1635T>G 4 153247167 STAD A G Missense p.F241L c.721T>C 4 153268087 CM A G Missense p.L301P c.902T>C 4 153253831 BRCA A G Missense p.W526R c.1576T>C 4 153247226 HNSC A G SpliceDonorSNV . c.584+2T>C 4 153271192 STAD A G Synonymous p.A315A c.945T>C 4 153253788 COREAD A G Synonymous p.L559L c.1677T>C 4 153245514 STAD AGTTACCTT - SpliceDonorDeletion . c.1120_1122+6delAAGGTAACT 4 153251878 HNSC AT - Frameshift p.M268Dfs*18 c.802_803delAT 4 153259012 UCEC A T Missense p.V143D c.428T>A 4 153332528 RCCC A T Missense p.V525E c.1574T>A 4 153247228 HNSC A T Nonsense p.L651* c.1952T>A 4 153244205 OV C A Missense p.D480Y c.1438G>T 4 153247364 LUAD C A Missense p.D600Y c.1798G>T 4 153245393 COREAD C A Missense p.E248D c.744G>T 4 153259071 UCEC C A Missense p.G423V c.1268G>T 4 153249510 ALL C A Missense p.G423V c.1268G>T 4 153249510 UCEC C A Missense p.G437V c.1310G>T 4 153249468 ALL C A Missense p.R441L c.1322G>T 4 153249456 BRCA C A Missense p.R484S c.1452G>T 4 153247350 HNSC C A Missense p.R505L c.1514G>T 4 153247288 HNSC C A Missense p.S476I c.1427G>T 4 153247375 UCEC C A Nonsense p.E655* c.1963G>T 4 153244194 LUSC C - Frameshift p.E471Kfs*27 c.1411delG 4 153249367 BLCA - C Frameshift p.S668Efs*26 c.2001dupG 4 153244156 LUSC C - Frameshift p.S668Vfs*39 c.2001delG 4 153244156 STAD C G Missense p.D520H c.1558G>C 4 153247244 HNSC C G Missense p.R479P c.1436G>C 4 153247366 BLCA C G Missense p.S585T c.1754G>C 4 153245437 LUSC C G Synonymous p.R674R c.2022G>C 4 153244135 RCCC C G Synonymous p.T653T c.1959G>C 4 153244198 LUSC C - IntronicDeletion . c.985+1delG 4 153253747 UCEC C T IntronicSNV . c.501+29113G>A 4 153303342 UCEC C T IntronicSNV . c.502-2757G>A 4 153274033 CLL C T Missense p.D520N c.1558G>A 4 153247244 COREAD C T Missense p.E332K c.994G>A 4 153252012 HNSC C T Missense p.G368E c.1103G>A 4 153251903 CM C T Missense p.G391D c.1172G>A 4 153250888 BRCA C T Missense p.G437R c.1309G>A 4 153249469 COREAD C T Missense p.G517E c.1550G>A 4 153247252 LUSC C T Missense p.G597E c.1790G>A 4 153245401 CLL C T Missense p.G687E c.2060G>A 4 153244097 MB C T Missense p.H540Y c.1618C>T 4 153247184 GBM C T Missense p.R357K c.1070G>A 4 153251936 BRCA C T Missense p.R441Q c.1322G>A 4 153249456 UCEC C T Missense p.R465H c.1394G>A 4 153249384 CLL C T Missense p.R465H c.1394G>A 4 153249384 COREAD C T Missense p.R465H c.1394G>A 4 153249384 LUAD C T Missense p.R465H c.1394G>A 4 153249384 LUSC C T Missense p.R465H c.1394G>A 4 153249384 OV C T Missense p.R465H c.1394G>A 4 153249384 UCEC C T Missense p.R479Q c.1436G>A 4 153247366 BRCA C T Missense p.R479Q c.1436G>A 4 153247366 CM C T Missense p.R479Q c.1436G>A 4 153247366 HNSC C T Missense p.R479Q c.1436G>A 4 153247366 STAD C T Missense p.R479Q c.1436G>A 4 153247366 UCEC C T Missense p.R505H c.1514G>A 4 153247288 COREAD C T Missense p.S516N c.1547G>A 4 153247255 HNSC C T Missense p.S582L c.1745C>T 4 153245446 COREAD C T Nonsense p.Q98* c.292C>T 4 153332664 COREAD C T Nonsense p.W321* c.963G>A 4 153253770 BLCA C T Synonymous p.K171K c.513G>A 4 153271265 STAD C T Synonymous p.L497L c.1491G>A 4 153247311 HNSC C T Synonymous p.T144T c.432G>A 4 153332524 ESCA G A IntronicSNV . c.502-2432C>T 4 153273708 UCEC G A Missense p.A502V c.1505C>T 4 153247297 HNSC G A Missense p.H500Y c.1498C>T 4 153247304 CM G A Missense p.P373S c.1117C>T 4 153251889 CM G A Missense p.R35C c.103C>T 4 153332853 HNSC G A Missense p.R465C c.1393C>T 4 153249385 COREAD G A Missense p.R465C c.1393C>T 4 153249385 ESCA G A Missense p.R465C c.1393C>T 4 153249385 MB G A Missense p.R465C c.1393C>T 4 153249385 STAD G A Missense p.R465C c.1393C>T 4 153249385 UCEC G A Missense p.R465H c.1394G>A 4 153249384 COREAD G A Missense p.R505C c.1513C>T 4 153247289 ALL G A Missense p.R505C c.1513C>T 4 153247289 CLL G A Missense p.R505C c.1513C>T 4 153247289 CM G A Missense p.R505C c.1513C>T 4 153247289 COREAD G A Missense p.R505C c.1513C>T 4 153247289 OV G A Missense p.R505C c.1513C>T 4 153247289 UCEC G A Missense p.R689W c.2065C>T 4 153244092 COREAD G A Missense p.R689W c.2065C>T 4 153244092 UCEC G A Missense p.S182F c.545C>T 4 153271233 CM G A Missense p.S227F c.680C>T 4 153268128 BRCA G A Missense p.S426L c.1277C>T 4 153249501 BLCA G A Missense p.S562L c.1685C>T 4 153245506 CM G A Missense p.S582L c.1745C>T 4 153245446 COREAD G A Missense p.S601F c.1802C>T 4 153245389 CM G A Missense p.T616I c.1847C>T 4 153245344 SCLC G A Missense p.T639I c.1916C>T 4 153244241 CM G A Nonsense p.Q120* c.358C>T 4 153332598 CM G A Nonsense p.Q612* c.1834C>T 4 153245357 MB G A Nonsense p.R13* c.37C>T 4 153332919 UCEC G A Nonsense p.R14* c.40C>T 4 153332916 UCEC G A Nonsense p.R224* c.670C>T 4 153268138 UCEC G A Nonsense p.R278* c.832C>T 4 153258983 ESCA G A Nonsense p.R278* c.832C>T 4 153258983 MB G A Nonsense p.R367* c.1099C>T 4 153251907 HNSC G A Nonsense p.R393* c.1177C>T 4 153250883 HNSC G A Nonsense p.R393* c.1177C>T 4 153250883 UCEC G A Nonsense p.R479* c.1435C>T 4 153247367 LUSC G A Nonsense p.R658* c.1972C>T 4 153244185 CM G A Nonsense p.R658* c.1972C>T 4 153244185 GBM G A Nonsense p.R658* c.1972C>T 4 153244185 UCEC G A Synonymous p.L296L c.886C>T 4 153253847 LUAD G C Missense p.P620R c.1859C>G 4 153244298 LUAD G C Missense p.R505G c.1513C>G 4 153247289 BLCA G C Missense p.R505G c.1513C>G 4 153247289 COREAD G C Missense p.R505G c.1513C>G 4 153247289 HNSC G C Missense p.R505G c.1513C>G 4 153247289 LUSC G C Missense p.R505G c.1513C>G 4 153247289 UCEC G C Nonsense p.S641* c.1922C>G 4 153244235 BLCA G C Nonsense p.S678* c.2033C>G 4 153244124 BLCA G C Synonymous p.V544V c.1632C>G 4 153247170 CM - G Frameshift p.Q581Pfs*24 c.1741dupC 4 153245450 BLCA G - Frameshift p.R309Afs*33 c.925delC 4 153253808 BRCA G T Missense p.F280L c.840C>A 4 153258975 CLL G T Missense p.R505L c.1514G>T 4 153247288 COREAD G T Missense p.R505S c.1513C>A 4 153247289 LUSC G T Missense p.S476R c.1428C>A 4 153247374 COREAD G T Missense p.T385K c.1154C>A 4 153250906 ALL G T Missense p.T385K c.1154C>A 4 153250906 BLCA G T Synonymous p.R479R c.1435C>A 4 153247367 LUSC G T Synonymous p.T456T c.1368C>A 4 153249410 LUSC T A Missense p.E287V c.860A>T 4 153258955 COREAD T A Missense p.N82Y c.244A>T 4 153332712 BRCA T A Nonsense p.R339* c.1015A>T 4 153251991 COREAD T C Missense p.D642G c.1925A>G 4 153244232 THCA T C Missense p.H379R c.1136A>G 4 153250924 LUAD T C Missense p.I563T c.1688T>C 4 153245503 PAAD T C Missense p.R543G c.1627A>G 4 153247175 HNSC T C Missense p.Y545C c.1634A>G 4 153247168 BRCA T C Missense p.Y545C c.1634A>G 4 153247168 UCEC - T Frameshift p.I605Nfs*39 c.1813dupA 4 153245378 STAD T G 3-UTRSNV . c.2121+193A>C 4 153243843 CM - TGAGT Frameshift p.I257Tfs*11 c.769_770insCTCAA 4 153259046 HNSC T G IntronicSNV . c.1-71615A>C 4 153404570 CLL T G Missense p.D129A c.386A>C 4 153332570 UCEC T G Missense p.H495P c.1484A>C 4 153247318 COREAD TGT - InFrameDeletion p.N401delN c.1202_1204delACA 4 153250856 COREAD