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 23 153176254 153176254 + Silent SNP A A G TCGA-OR-A5KZ-01A-11D-A29I-10 TCGA-OR-A5KZ-10A-01D-A29L-10 g.chrX:153176254A>G c.1716T>C c.(1714-1716)caT>caC p.H572H ACC 23 153184648 153184648 + Silent SNP G G T TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chrX:153184648G>T c.771C>A c.(769-771)gtC>gtA p.V257V ACC 23 153187251 153187251 + Missense_Mutation SNP G G T TCGA-OR-A5K2-01A-11D-A29I-10 TCGA-OR-A5K2-10B-01D-A29L-10 g.chrX:153187251G>T c.79C>A c.(79-81)Cag>Aag p.Q27K BLCA 23 153178221 153178221 + Missense_Mutation SNP C C T TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chrX:153178221C>T c.1475G>A c.(1474-1476)cGc>cAc p.R492H BLCA 23 153179046 153179046 + Missense_Mutation SNP C C G TCGA-FD-A5C1-01A-11D-A289-08 TCGA-FD-A5C1-10A-01D-A289-08 g.chrX:153179046C>G c.1143G>C c.(1141-1143)aaG>aaC p.K381N BLCA 23 153186824 153186824 + Silent SNP G G A TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chrX:153186824G>A c.429C>T c.(427-429)gtC>gtT p.V143V BLCA 23 153186957 153186957 + Missense_Mutation SNP G G C TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chrX:153186957G>C c.296C>G c.(295-297)cCc>cGc p.P99R BRCA 23 153173249 153173250 + Frame_Shift_Ins INS - - G TCGA-AN-A0FX-01A-11W-A050-09 TCGA-AN-A0FX-10A-01W-A055-09 g.chrX:153173249_153173250insG c.2774_2775insC c.(2773-2775)cctfs p.P925fs BRCA 23 153174974 153174974 + Silent SNP C C A TCGA-C8-A26X-01A-31D-A16D-09 TCGA-C8-A26X-10A-01D-A16D-09 g.chrX:153174974C>A c.2430G>T c.(2428-2430)gtG>gtT p.V810V BRCA 23 153175227 153175227 + Silent SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:153175227G>A c.2382C>T c.(2380-2382)ctC>ctT p.L794L BRCA 23 153176593 153176593 + Missense_Mutation SNP G G C TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chrX:153176593G>C c.1593C>G c.(1591-1593)atC>atG p.I531M BRCA 23 153184655 153184655 + Missense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chrX:153184655G>A c.764C>T c.(763-765)gCt>gTt p.A255V CESC 23 153176375 153176375 + Splice_Site SNP C C G TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chrX:153176375C>G c.e14+1 CESC 23 153176611 153176611 + Missense_Mutation SNP C C G TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chrX:153176611C>G c.1575G>C c.(1573-1575)gaG>gaC p.E525D CESC 23 153178166 153178166 + Missense_Mutation SNP C C G TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chrX:153178166C>G c.1530G>C c.(1528-1530)gaG>gaC p.E510D CESC 23 153186187 153186187 + Nonsense_Mutation SNP C C A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chrX:153186187C>A c.574G>T c.(574-576)Gag>Tag p.E192* CESC 23 153186238 153186238 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chrX:153186238G>C c.523C>G c.(523-525)Cac>Gac p.H175D CESC 23 153187188 153187188 + Missense_Mutation SNP C C G TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chrX:153187188C>G c.142G>C c.(142-144)Gag>Cag p.E48Q COAD 23 153175289 153175289 + Missense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chrX:153175289G>A c.2320C>T c.(2320-2322)Cgg>Tgg p.R774W COAD 23 153175378 153175378 + Splice_Site SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:153175378T>C c.2231A>G c.(2230-2232)gAc>gGc p.D744G COAD 23 153175663 153175663 + Silent SNP G G A TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chrX:153175663G>A c.2118C>T c.(2116-2118)taC>taT p.Y706Y COAD 23 153178188 153178188 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:153178188C>A c.1508G>T c.(1507-1509)aGa>aTa p.R503I COAD 23 153178222 153178222 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chrX:153178222G>A c.1474C>T c.(1474-1476)Cgc>Tgc p.R492C COAD 23 153178995 153178995 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:153178995G>A c.1194C>T c.(1192-1194)gaC>gaT p.D398D COAD 23 153184343 153184343 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:153184343A>G c.975T>C c.(973-975)caT>caC p.H325H COAD 23 153184643 153184643 + Missense_Mutation SNP T T A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:153184643T>A c.776A>T c.(775-777)aAc>aTc p.N259I COAD 23 153185114 153185114 + Intron SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:153185114G>A COAD 23 153187059 153187059 + Splice_Site SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:153187059G>A c.271C>T c.(271-273)Cgg>Tgg p.R91W COAD 23 153187088 153187088 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chrX:153187088A>G c.242T>C c.(241-243)cTg>cCg p.L81P COADREAD 23 153175289 153175289 + Missense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chrX:153175289G>A c.2320C>T c.(2320-2322)Cgg>Tgg p.R774W COADREAD 23 153175378 153175378 + Splice_Site SNP T T C TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:153175378T>C c.2231A>G c.(2230-2232)gAc>gGc p.D744G COADREAD 23 153175663 153175663 + Silent SNP G G A TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chrX:153175663G>A c.2118C>T c.(2116-2118)taC>taT p.Y706Y COADREAD 23 153178188 153178188 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:153178188C>A c.1508G>T c.(1507-1509)aGa>aTa p.R503I COADREAD 23 153178222 153178222 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chrX:153178222G>A c.1474C>T c.(1474-1476)Cgc>Tgc p.R492C COADREAD 23 153178995 153178995 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:153178995G>A c.1194C>T c.(1192-1194)gaC>gaT p.D398D COADREAD 23 153184343 153184343 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:153184343A>G c.975T>C c.(973-975)caT>caC p.H325H COADREAD 23 153184643 153184643 + Missense_Mutation SNP T T A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chrX:153184643T>A c.776A>T c.(775-777)aAc>aTc p.N259I COADREAD 23 153185114 153185114 + Intron SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:153185114G>A COADREAD 23 153187059 153187059 + Splice_Site SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:153187059G>A c.271C>T c.(271-273)Cgg>Tgg p.R91W COADREAD 23 153187088 153187088 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chrX:153187088A>G c.242T>C c.(241-243)cTg>cCg p.L81P GBM 23 153175809 153175809 + Missense_Mutation SNP C C T TCGA-76-6661-01B-11D-1845-08 TCGA-76-6661-10A-01D-1845-08 g.chrX:153175809C>T c.1972G>A c.(1972-1974)Gtg>Atg p.V658M GBM 23 153184317 153184317 + Missense_Mutation SNP C C T TCGA-14-0813-01A-01W-0424-08 TCGA-14-0813-10A-01W-0424-08 g.chrX:153184317C>T c.1001G>A c.(1000-1002)cGc>cAc p.R334H GBMLGG 23 153173283 153173283 + Missense_Mutation SNP C C T TCGA-KT-A7W1-01A-11D-A34A-08 TCGA-KT-A7W1-10A-01D-A34A-08 g.chrX:153173283C>T c.2741G>A c.(2740-2742)cGc>cAc p.R914H GBMLGG 23 153175536 153175536 + Silent SNP G G A TCGA-DH-5144-01A-01D-1468-08 TCGA-DH-5144-10A-01D-1468-08 g.chrX:153175536G>A c.2160C>T c.(2158-2160)gaC>gaT p.D720D GBMLGG 23 153175809 153175809 + Missense_Mutation SNP C C T TCGA-76-6661-01B-11D-1845-08 TCGA-76-6661-10A-01D-1845-08 g.chrX:153175809C>T c.1972G>A c.(1972-1974)Gtg>Atg p.V658M GBMLGG 23 153176003 153176003 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:153176003G>A c.1879C>T c.(1879-1881)Ccg>Tcg p.P627S GBMLGG 23 153184317 153184317 + Missense_Mutation SNP C C T TCGA-14-0813-01A-01W-0424-08 TCGA-14-0813-10A-01W-0424-08 g.chrX:153184317C>T c.1001G>A c.(1000-1002)cGc>cAc p.R334H HNSC 23 153175297 153175297 + Missense_Mutation SNP T T C TCGA-CN-5370-01A-01D-2012-08 TCGA-CN-5370-10A-01D-2013-08 g.chrX:153175297T>C c.2312A>G c.(2311-2313)gAc>gGc p.D771G HNSC 23 153176046 153176046 + Missense_Mutation SNP C C G TCGA-UF-A71A-01A-22D-A34J-08 TCGA-UF-A71A-10A-01D-A34M-08 g.chrX:153176046C>G c.1836G>C c.(1834-1836)gaG>gaC p.E612D HNSC 23 153178174 153178174 + Missense_Mutation SNP C C T TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chrX:153178174C>T c.1522G>A c.(1522-1524)Gac>Aac p.D508N HNSC 23 153178184 153178184 + Silent SNP G G C TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chrX:153178184G>C c.1512C>G c.(1510-1512)ctC>ctG p.L504L HNSC 23 153178233 153178233 + Missense_Mutation SNP A A T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:153178233A>T c.1463T>A c.(1462-1464)tTc>tAc p.F488Y HNSC 23 153178906 153178906 + Missense_Mutation SNP C C T TCGA-BB-8596-01A-11D-2394-08 TCGA-BB-8596-10A-01D-2394-08 g.chrX:153178906C>T c.1283G>A c.(1282-1284)cGg>cAg p.R428Q HNSC 23 153178914 153178914 + Missense_Mutation SNP C C A TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chrX:153178914C>A c.1275G>T c.(1273-1275)caG>caT p.Q425H HNSC 23 153178994 153178994 + Missense_Mutation SNP C C T TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chrX:153178994C>T c.1195G>A c.(1195-1197)Ggg>Agg p.G399R HNSC 23 153184378 153184378 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:153184378G>A c.940C>T c.(940-942)Cct>Tct p.P314S HNSC 23 153184449 153184449 + Missense_Mutation SNP G G T TCGA-UF-A7JJ-01A-11D-A34J-08 TCGA-UF-A7JJ-10A-01D-A34M-08 g.chrX:153184449G>T c.869C>A c.(868-870)gCt>gAt p.A290D HNSC 23 153184627 153184627 + Silent SNP G G A TCGA-UF-A71B-01A-12D-A34J-08 TCGA-UF-A71B-10B-01D-A34M-08 g.chrX:153184627G>A c.792C>T c.(790-792)gaC>gaT p.D264D HNSC 23 153186904 153186904 + Missense_Mutation SNP T T A TCGA-CV-6950-01A-11D-1912-08 TCGA-CV-6950-10A-01D-1912-08 g.chrX:153186904T>A c.349A>T c.(349-351)Agc>Tgc p.S117C LGG 23 153173283 153173283 + Missense_Mutation SNP C C T TCGA-KT-A7W1-01A-11D-A34A-08 TCGA-KT-A7W1-10A-01D-A34A-08 g.chrX:153173283C>T c.2741G>A c.(2740-2742)cGc>cAc p.R914H LGG 23 153175536 153175536 + Silent SNP G G A TCGA-DH-5144-01A-01D-1468-08 TCGA-DH-5144-10A-01D-1468-08 g.chrX:153175536G>A c.2160C>T c.(2158-2160)gaC>gaT p.D720D LGG 23 153176003 153176003 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:153176003G>A c.1879C>T c.(1879-1881)Ccg>Tcg p.P627S LIHC 23 153173335 153173335 + Missense_Mutation SNP T T A TCGA-DD-AAVV-01A-11D-A40R-10 TCGA-DD-AAVV-10A-01D-A40U-10 g.chrX:153173335T>A c.2689A>T c.(2689-2691)Acc>Tcc p.T897S LIHC 23 153173337 153173337 + Missense_Mutation SNP G G A TCGA-DD-AAVV-01A-11D-A40R-10 TCGA-DD-AAVV-10A-01D-A40U-10 g.chrX:153173337G>A c.2687C>T c.(2686-2688)tCt>tTt p.S896F LIHC 23 153174961 153174961 + Silent SNP G G A TCGA-NI-A8LF-01A-11D-A35Z-10 TCGA-NI-A8LF-10A-01D-A35Z-10 g.chrX:153174961G>A c.2443C>T c.(2443-2445)Ctg>Ttg p.L815L LIHC 23 153185069 153185069 + Intron SNP G G T TCGA-DD-A118-01A-11D-A12Z-10 TCGA-DD-A118-11A-11D-A12Z-10 g.chrX:153185069G>T LUAD 23 153173206 153173206 + Missense_Mutation SNP C C G TCGA-55-6543-01A-11D-1753-08 TCGA-55-6543-10A-01D-1753-08 g.chrX:153173206C>G c.2818G>C c.(2818-2820)Gac>Cac p.D940H LUAD 23 153175377 153175377 + Splice_Site SNP G G A TCGA-86-8075-01A-11D-2238-08 TCGA-86-8075-10A-01D-2238-08 g.chrX:153175377G>A c.2232C>T c.(2230-2232)gaC>gaT p.D744D LUAD 23 153176039 153176039 + Nonsense_Mutation SNP C C A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chrX:153176039C>A c.1843G>T c.(1843-1845)Gag>Tag p.E615* LUAD 23 153178174 153178174 + Missense_Mutation SNP C C G TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chrX:153178174C>G c.1522G>C c.(1522-1524)Gac>Cac p.D508H LUAD 23 153178193 153178193 + Missense_Mutation SNP G G T TCGA-55-6970-01A-11D-1945-08 TCGA-55-6970-11A-01D-1945-08 g.chrX:153178193G>T c.1503C>A c.(1501-1503)aaC>aaA p.N501K LUAD 23 153178971 153178971 + Missense_Mutation SNP C C G TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chrX:153178971C>G c.1218G>C c.(1216-1218)caG>caC p.Q406H LUAD 23 153184317 153184317 + Missense_Mutation SNP C C A TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chrX:153184317C>A c.1001G>T c.(1000-1002)cGc>cTc p.R334L LUAD 23 153184318 153184318 + Missense_Mutation SNP G G A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chrX:153184318G>A c.1000C>T c.(1000-1002)Cgc>Tgc p.R334C LUAD 23 153184369 153184369 + Missense_Mutation SNP C C A TCGA-78-7163-01A-12D-2063-08 TCGA-78-7163-11A-01D-2063-08 g.chrX:153184369C>A c.949G>T c.(949-951)Gac>Tac p.D317Y LUAD 23 153184454 153184454 + Silent SNP C C T TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chrX:153184454C>T c.864G>A c.(862-864)acG>acA p.T288T LUAD 23 153184609 153184609 + Splice_Site SNP G G A TCGA-55-7724-01A-11D-2167-08 TCGA-55-7724-10A-01D-2167-08 g.chrX:153184609G>A c.810C>T c.(808-810)gaC>gaT p.D270D LUAD 23 153186130 153186130 + Missense_Mutation SNP C C T TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chrX:153186130C>T c.631G>A c.(631-633)Ggg>Agg p.G211R LUAD 23 153186252 153186252 + Missense_Mutation SNP G G A TCGA-50-5935-01A-11D-1753-08 TCGA-50-5935-11A-01D-1753-08 g.chrX:153186252G>A c.509C>T c.(508-510)aCg>aTg p.T170M LUAD 23 153186551 153186551 + Splice_Site SNP G G A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chrX:153186551G>A c.497C>T c.(496-498)aCg>aTg p.T166M LUAD 23 153187084 153187084 + Frame_Shift_Del DEL C C - TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chrX:153187084delC c.246delG c.(244-246)gggfs p.G82fs LUSC 23 153173229 153173229 + Nonsense_Mutation SNP G G C TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chrX:153173229G>C c.2795C>G c.(2794-2796)tCa>tGa p.S932* LUSC 23 153173337 153173337 + Missense_Mutation SNP G G C TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chrX:153173337G>C c.2687C>G c.(2686-2688)tCt>tGt p.S896C OV 23 153173342 153173342 + Silent SNP T T C TCGA-36-2545-01A-01D-1526-09 TCGA-36-2545-10A-01D-1526-09 g.chrX:153173342T>C c.2682A>G c.(2680-2682)ccA>ccG p.P894P OV 23 153175368 153175368 + Silent SNP C C G TCGA-13-2057-01A-02D-1526-09 TCGA-13-2057-10A-01D-1526-09 g.chrX:153175368C>G c.2241G>C c.(2239-2241)ggG>ggC p.G747G PAAD 23 153173252 153173253 + Frame_Shift_Ins INS - - C TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chrX:153173252_153173253insC c.2771_2772insG c.(2770-2772)ggcfs p.G924fs PAAD 23 153187163 153187163 + Missense_Mutation SNP C C T TCGA-OE-A75W-01A-12D-A32N-08 TCGA-OE-A75W-10A-01D-A32N-08 g.chrX:153187163C>T c.167G>A c.(166-168)cGc>cAc p.R56H PRAD 23 153187219 153187219 + Silent SNP C C A TCGA-HC-7752-01A-11D-2114-08 TCGA-HC-7752-10A-01D-2115-08 g.chrX:153187219C>A c.111G>T c.(109-111)ctG>ctT p.L37L SKCM 23 153174589 153174589 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:153174589G>A c.2542C>T c.(2542-2544)Ccc>Tcc p.P848S SKCM 23 153175712 153175712 + Missense_Mutation SNP T T G TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chrX:153175712T>G c.2069A>C c.(2068-2070)cAg>cCg p.Q690P SKCM 23 153184723 153184723 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:153184723G>A c.696C>T c.(694-696)ttC>ttT p.F232F SKCM 23 153186111 153186111 + Missense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chrX:153186111G>A c.650C>T c.(649-651)tCc>tTc p.S217F SKCM 23 153186550 153186550 + Splice_Site SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chrX:153186550C>T c.498G>A c.(496-498)acG>acA p.T166T SKCM 23 153191630 153191630 + Silent SNP C C T TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chrX:153191630C>T c.27G>A c.(25-27)cgG>cgA p.R9R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US X 153187058 153187058 single base substitution C T missense_variant R68Q 203G>A AML-US X 153187058 153187058 single base substitution C T missense_variant R91Q 272G>A AML-US X 153187058 153187058 single base substitution C T splice_region_variant AML-US X 153187058 153187058 single base substitution C T upstream_gene_variant BLCA-CN X 153171550 153171550 single base substitution C T downstream_gene_variant BLCA-US X 153171751 153171751 single base substitution C T downstream_gene_variant BOCA-FR X 153178514 153178514 single base substitution T C downstream_gene_variant BOCA-FR X 153178514 153178514 single base substitution T C intron_variant BOCA-FR X 153178514 153178514 single base substitution T C upstream_gene_variant BOCA-FR X 153187384 153187384 single base substitution C T intron_variant BOCA-FR X 153187384 153187384 single base substitution C T upstream_gene_variant BRCA-EU X 153167855 153167855 single base substitution G A downstream_gene_variant BRCA-EU X 153168281 153168281 single base substitution G A downstream_gene_variant BRCA-EU X 153168454 153168454 single base substitution C G downstream_gene_variant BRCA-EU X 153170158 153170158 single base substitution G A downstream_gene_variant BRCA-EU X 153170241 153170241 single base substitution T A downstream_gene_variant BRCA-EU X 153170684 153170684 single base substitution C T downstream_gene_variant BRCA-EU X 153171521 153171521 single base substitution C T downstream_gene_variant BRCA-EU X 153172137 153172137 single base substitution C T downstream_gene_variant BRCA-EU X 153173201 153173201 single base substitution C T 3_prime_UTR_variant BRCA-EU X 153173201 153173201 single base substitution C T downstream_gene_variant BRCA-EU X 153173201 153173201 single base substitution C T exon_variant BRCA-EU X 153173201 153173201 single base substitution C T synonymous_variant T763T 2289G>A BRCA-EU X 153173201 153173201 single base substitution C T synonymous_variant T918T 2754G>A BRCA-EU X 153173201 153173201 single base substitution C T synonymous_variant T920T 2760G>A BRCA-EU X 153173201 153173201 single base substitution C T synonymous_variant T941T 2823G>A BRCA-EU X 153173201 153173201 single base substitution C T synonymous_variant T981T 2943G>A BRCA-EU X 153173310 153173310 single base substitution C T 3_prime_UTR_variant BRCA-EU X 153173310 153173310 single base substitution C T downstream_gene_variant BRCA-EU X 153173310 153173310 single base substitution C T exon_variant BRCA-EU X 153173310 153173310 single base substitution C T missense_variant R727Q 2180G>A BRCA-EU X 153173310 153173310 single base substitution C T missense_variant R882Q 2645G>A BRCA-EU X 153173310 153173310 single base substitution C T missense_variant R884Q 2651G>A BRCA-EU X 153173310 153173310 single base substitution C T missense_variant R905Q 2714G>A BRCA-EU X 153173310 153173310 single base substitution C T missense_variant R945Q 2834G>A BRCA-EU X 153173610 153173610 single base substitution C T downstream_gene_variant BRCA-EU X 153173610 153173610 single base substitution C T intron_variant BRCA-EU X 153173731 153173731 single base substitution C T downstream_gene_variant BRCA-EU X 153173731 153173731 single base substitution C T intron_variant BRCA-EU X 153174879 153174879 single base substitution C G downstream_gene_variant BRCA-EU X 153174879 153174879 single base substitution C G intron_variant BRCA-EU X 153177319 153177319 single base substitution G A downstream_gene_variant BRCA-EU X 153177319 153177319 single base substitution G A intron_variant BRCA-EU X 153177319 153177319 single base substitution G A upstream_gene_variant BRCA-EU X 153177550 153177550 single base substitution C G downstream_gene_variant BRCA-EU X 153177550 153177550 single base substitution C G intron_variant BRCA-EU X 153177550 153177550 single base substitution C G upstream_gene_variant BRCA-EU X 153178195 153178195 single base substitution T C 3_prime_UTR_variant BRCA-EU X 153178195 153178195 single base substitution T C downstream_gene_variant BRCA-EU X 153178195 153178195 single base substitution T C exon_variant BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N15D 43A>G BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N323D 967A>G BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N478D 1432A>G BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N480D 1438A>G BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N501D 1501A>G BRCA-EU X 153178195 153178195 single base substitution T C missense_variant N541D 1621A>G BRCA-EU X 153178195 153178195 single base substitution T C upstream_gene_variant BRCA-EU X 153178816 153178816 single base substitution C G downstream_gene_variant BRCA-EU X 153178816 153178816 single base substitution C G exon_variant BRCA-EU X 153178816 153178816 single base substitution C G intron_variant BRCA-EU X 153178816 153178816 single base substitution C G upstream_gene_variant BRCA-EU X 153179326 153179326 single base substitution T A 3_prime_UTR_variant BRCA-EU X 153179326 153179326 single base substitution T A downstream_gene_variant BRCA-EU X 153179326 153179326 single base substitution T A exon_variant BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E122V 365A>T BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E169V 506A>T BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E324V 971A>T BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E326V 977A>T BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E347V 1040A>T BRCA-EU X 153179326 153179326 single base substitution T A missense_variant E387V 1160A>T BRCA-EU X 153179326 153179326 single base substitution T A upstream_gene_variant BRCA-EU X 153180332 153180332 single base substitution C A downstream_gene_variant BRCA-EU X 153180332 153180332 single base substitution C A intron_variant BRCA-EU X 153180332 153180332 single base substitution C A upstream_gene_variant BRCA-EU X 153182073 153182073 single base substitution A T downstream_gene_variant BRCA-EU X 153182073 153182073 single base substitution A T intron_variant BRCA-EU X 153182073 153182073 single base substitution A T upstream_gene_variant BRCA-EU X 153182139 153182139 single base substitution G C downstream_gene_variant BRCA-EU X 153182139 153182139 single base substitution G C intron_variant BRCA-EU X 153182139 153182139 single base substitution G C upstream_gene_variant BRCA-EU X 153182690 153182690 single base substitution A T downstream_gene_variant BRCA-EU X 153182690 153182690 single base substitution A T intron_variant BRCA-EU X 153182690 153182690 single base substitution A T upstream_gene_variant BRCA-EU X 153182795 153182795 single base substitution C T downstream_gene_variant BRCA-EU X 153182795 153182795 single base substitution C T intron_variant BRCA-EU X 153182795 153182795 single base substitution C T upstream_gene_variant BRCA-EU X 153184377 153184377 single base substitution G T 3_prime_UTR_variant BRCA-EU X 153184377 153184377 single base substitution G T downstream_gene_variant BRCA-EU X 153184377 153184377 single base substitution G T exon_variant BRCA-EU X 153184377 153184377 single base substitution G T intron_variant BRCA-EU X 153184377 153184377 single base substitution G T missense_variant P291H 872C>A BRCA-EU X 153184377 153184377 single base substitution G T missense_variant P293H 878C>A BRCA-EU X 153184377 153184377 single base substitution G T missense_variant P314H 941C>A BRCA-EU X 153184377 153184377 single base substitution G T missense_variant P354H 1061C>A BRCA-EU X 153184377 153184377 single base substitution G T missense_variant P89H 266C>A BRCA-EU X 153184377 153184377 single base substitution G T upstream_gene_variant BRCA-EU X 153184569 153184569 single base substitution G T downstream_gene_variant BRCA-EU X 153184569 153184569 single base substitution G T intron_variant BRCA-EU X 153184569 153184569 single base substitution G T upstream_gene_variant BRCA-EU X 153188682 153188682 single base substitution A T intron_variant BRCA-EU X 153188682 153188682 single base substitution A T upstream_gene_variant BRCA-EU X 153190794 153190794 single base substitution C T intron_variant BRCA-EU X 153190794 153190794 single base substitution C T upstream_gene_variant BRCA-EU X 153191295 153191295 single base substitution C G intron_variant BRCA-EU X 153191295 153191295 single base substitution C G upstream_gene_variant BRCA-EU X 153191680 153191680 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU X 153191680 153191680 single base substitution G A exon_variant BRCA-EU X 153191680 153191680 single base substitution G A intron_variant BRCA-EU X 153191680 153191680 single base substitution G A upstream_gene_variant BRCA-EU X 153192060 153192060 single base substitution G T 5_prime_UTR_variant BRCA-EU X 153192060 153192060 single base substitution G T intron_variant BRCA-EU X 153192060 153192060 single base substitution G T upstream_gene_variant BRCA-EU X 153193056 153193056 single base substitution C G intron_variant BRCA-EU X 153193056 153193056 single base substitution C G upstream_gene_variant BRCA-EU X 153193965 153193965 single base substitution C G intron_variant BRCA-EU X 153193965 153193965 single base substitution C G upstream_gene_variant BRCA-EU X 153194600 153194600 single base substitution G A intron_variant BRCA-EU X 153194600 153194600 single base substitution G A upstream_gene_variant BRCA-EU X 153196205 153196205 single base substitution C T intron_variant BRCA-EU X 153196205 153196205 single base substitution C T upstream_gene_variant BRCA-EU X 153197468 153197468 single base substitution G C intron_variant BRCA-EU X 153197468 153197468 single base substitution G C upstream_gene_variant BRCA-EU X 153199120 153199120 single base substitution G A intron_variant BRCA-EU X 153200073 153200073 single base substitution G A intron_variant BRCA-EU X 153201241 153201241 single base substitution G C upstream_gene_variant BRCA-EU X 153202829 153202829 single base substitution T G upstream_gene_variant BRCA-EU X 153203194 153203194 single base substitution C T upstream_gene_variant BRCA-EU X 153203634 153203634 single base substitution C G upstream_gene_variant BRCA-EU X 153204364 153204364 single base substitution T A upstream_gene_variant BRCA-EU X 153204791 153204791 single base substitution C A upstream_gene_variant BRCA-EU X 153204791 153204791 single base substitution C T upstream_gene_variant BRCA-FR X 153167855 153167855 single base substitution G A downstream_gene_variant BRCA-FR X 153168024 153168024 single base substitution G T downstream_gene_variant BRCA-FR X 153173201 153173201 single base substitution C T 3_prime_UTR_variant BRCA-FR X 153173201 153173201 single base substitution C T downstream_gene_variant BRCA-FR X 153173201 153173201 single base substitution C T exon_variant BRCA-FR X 153173201 153173201 single base substitution C T synonymous_variant T763T 2289G>A BRCA-FR X 153173201 153173201 single base substitution C T synonymous_variant T918T 2754G>A BRCA-FR X 153173201 153173201 single base substitution C T synonymous_variant T920T 2760G>A BRCA-FR X 153173201 153173201 single base substitution C T synonymous_variant T941T 2823G>A BRCA-FR X 153173201 153173201 single base substitution C T synonymous_variant T981T 2943G>A BRCA-FR X 153173728 153173728 single base substitution G A downstream_gene_variant BRCA-FR X 153173728 153173728 single base substitution G A intron_variant BRCA-FR X 153177433 153177433 single base substitution G A downstream_gene_variant BRCA-FR X 153177433 153177433 single base substitution G A intron_variant BRCA-FR X 153177433 153177433 single base substitution G A upstream_gene_variant BRCA-FR X 153177550 153177550 single base substitution C G downstream_gene_variant BRCA-FR X 153177550 153177550 single base substitution C G intron_variant BRCA-FR X 153177550 153177550 single base substitution C G upstream_gene_variant BRCA-FR X 153180198 153180198 single base substitution G A downstream_gene_variant BRCA-FR X 153180198 153180198 single base substitution G A intron_variant BRCA-FR X 153180198 153180198 single base substitution G A upstream_gene_variant BRCA-FR X 153180332 153180332 single base substitution C A downstream_gene_variant BRCA-FR X 153180332 153180332 single base substitution C A intron_variant BRCA-FR X 153180332 153180332 single base substitution C A upstream_gene_variant BRCA-FR X 153182139 153182139 single base substitution G C downstream_gene_variant BRCA-FR X 153182139 153182139 single base substitution G C intron_variant BRCA-FR X 153182139 153182139 single base substitution G C upstream_gene_variant BRCA-FR X 153191017 153191017 single base substitution C T intron_variant BRCA-FR X 153191017 153191017 single base substitution C T upstream_gene_variant BRCA-FR X 153191295 153191295 single base substitution C G intron_variant BRCA-FR X 153191295 153191295 single base substitution C G upstream_gene_variant BRCA-FR X 153193056 153193056 single base substitution C G intron_variant BRCA-FR X 153193056 153193056 single base substitution C G upstream_gene_variant BRCA-FR X 153203634 153203634 single base substitution C G upstream_gene_variant BRCA-KR X 153175559 153175559 single base substitution G A downstream_gene_variant BRCA-KR X 153175559 153175559 single base substitution G A exon_variant BRCA-KR X 153175559 153175559 single base substitution G A intron_variant BRCA-KR X 153175559 153175559 single base substitution G A upstream_gene_variant BRCA-UK X 153168454 153168454 single base substitution C G downstream_gene_variant BRCA-UK X 153184569 153184569 single base substitution G T downstream_gene_variant BRCA-UK X 153184569 153184569 single base substitution G T intron_variant BRCA-UK X 153184569 153184569 single base substitution G T upstream_gene_variant BRCA-UK X 153187822 153187822 single base substitution G A intron_variant BRCA-UK X 153187822 153187822 single base substitution G A upstream_gene_variant BRCA-UK X 153199408 153199408 single base substitution A C exon_variant BRCA-US X 153171405 153171405 single base substitution C T downstream_gene_variant BRCA-US X 153171699 153171699 single base substitution C T downstream_gene_variant BRCA-US X 153172076 153172076 single base substitution G A downstream_gene_variant BRCA-US X 153173249 153173249 insertion of <=200bp - G 3_prime_UTR_variant BRCA-US X 153173249 153173249 insertion of <=200bp - G downstream_gene_variant BRCA-US X 153173249 153173249 insertion of <=200bp - G exon_variant BRCA-US X 153173249 153173249 insertion of <=200bp - G frameshift_variant P747P? BRCA-US X 153173249 153173249 insertion of <=200bp - G frameshift_variant P902P? BRCA-US X 153173249 153173249 insertion of <=200bp - G frameshift_variant P904P? BRCA-US X 153173249 153173249 insertion of <=200bp - G frameshift_variant P925P? BRCA-US X 153173249 153173249 insertion of <=200bp - G frameshift_variant P965P? BRCA-US X 153174928 153174928 deletion of <=200bp C - 3_prime_UTR_variant BRCA-US X 153174928 153174928 deletion of <=200bp C - downstream_gene_variant BRCA-US X 153174928 153174928 deletion of <=200bp C - exon_variant BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E247 BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E648 BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E803 BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E805 BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E826 BRCA-US X 153174928 153174928 deletion of <=200bp C - frameshift_variant E866 BRCA-US X 153174974 153174974 single base substitution C A 3_prime_UTR_variant BRCA-US X 153174974 153174974 single base substitution C A downstream_gene_variant BRCA-US X 153174974 153174974 single base substitution C A exon_variant BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V231V 693G>T BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V632V 1896G>T BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V787V 2361G>T BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V789V 2367G>T BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V810V 2430G>T BRCA-US X 153174974 153174974 single base substitution C A synonymous_variant V850V 2550G>T BRCA-US X 153175227 153175227 single base substitution G A 3_prime_UTR_variant BRCA-US X 153175227 153175227 single base substitution G A downstream_gene_variant BRCA-US X 153175227 153175227 single base substitution G A exon_variant BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L215L 645C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L282L 846C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L616L 1848C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L771L 2313C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L773L 2319C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L794L 2382C>T BRCA-US X 153175227 153175227 single base substitution G A synonymous_variant L834L 2502C>T BRCA-US X 153175227 153175227 single base substitution G A upstream_gene_variant BRCA-US X 153176593 153176593 single base substitution G C 3_prime_UTR_variant BRCA-US X 153176593 153176593 single base substitution G C downstream_gene_variant BRCA-US X 153176593 153176593 single base substitution G C exon_variant BRCA-US X 153176593 153176593 single base substitution G C missense_variant I353M 1059C>G BRCA-US X 153176593 153176593 single base substitution G C missense_variant I45M 135C>G BRCA-US X 153176593 153176593 single base substitution G C missense_variant I508M 1524C>G BRCA-US X 153176593 153176593 single base substitution G C missense_variant I510M 1530C>G BRCA-US X 153176593 153176593 single base substitution G C missense_variant I531M 1593C>G BRCA-US X 153176593 153176593 single base substitution G C missense_variant I571M 1713C>G BRCA-US X 153176593 153176593 single base substitution G C upstream_gene_variant BRCA-US X 153184655 153184655 single base substitution G A 3_prime_UTR_variant BRCA-US X 153184655 153184655 single base substitution G A downstream_gene_variant BRCA-US X 153184655 153184655 single base substitution G A exon_variant BRCA-US X 153184655 153184655 single base substitution G A intron_variant BRCA-US X 153184655 153184655 single base substitution G A missense_variant A142V 425C>T BRCA-US X 153184655 153184655 single base substitution G A missense_variant A232V 695C>T BRCA-US X 153184655 153184655 single base substitution G A missense_variant A234V 701C>T BRCA-US X 153184655 153184655 single base substitution G A missense_variant A255V 764C>T BRCA-US X 153184655 153184655 single base substitution G A missense_variant A295V 884C>T BRCA-US X 153184655 153184655 single base substitution G A missense_variant A30V 89C>T BRCA-US X 153184655 153184655 single base substitution G A upstream_gene_variant BRCA-US X 153197767 153197767 single base substitution A C splice_donor_variant BRCA-US X 153197767 153197767 single base substitution A C upstream_gene_variant BRCA-US X 153197829 153197829 single base substitution G T exon_variant BRCA-US X 153197829 153197829 single base substitution G T upstream_gene_variant BRCA-US X 153197996 153197996 single base substitution G A exon_variant BRCA-US X 153197996 153197996 single base substitution G A upstream_gene_variant BTCA-JP X 153171401 153171401 single base substitution G A downstream_gene_variant BTCA-JP X 153172147 153172147 single base substitution G A downstream_gene_variant BTCA-JP X 153174891 153174891 single base substitution G C downstream_gene_variant BTCA-JP X 153174891 153174891 single base substitution G C intron_variant BTCA-JP X 153174891 153174891 single base substitution G C splice_region_variant BTCA-JP X 153174892 153174892 single base substitution C T downstream_gene_variant BTCA-JP X 153174892 153174892 single base substitution C T intron_variant BTCA-JP X 153174892 153174892 single base substitution C T splice_region_variant BTCA-JP X 153175201 153175201 single base substitution G C 3_prime_UTR_variant BTCA-JP X 153175201 153175201 single base substitution G C downstream_gene_variant BTCA-JP X 153175201 153175201 single base substitution G C exon_variant BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P224R 671C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P291R 872C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P625R 1874C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P780R 2339C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P782R 2345C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P803R 2408C>G BTCA-JP X 153175201 153175201 single base substitution G C missense_variant P843R 2528C>G BTCA-JP X 153175201 153175201 single base substitution G C upstream_gene_variant BTCA-JP X 153175663 153175663 single base substitution G A 3_prime_UTR_variant BTCA-JP X 153175663 153175663 single base substitution G A downstream_gene_variant BTCA-JP X 153175663 153175663 single base substitution G A exon_variant BTCA-JP X 153175663 153175663 single base substitution G A intron_variant BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y194Y 582C>T BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y528Y 1584C>T BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y683Y 2049C>T BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y685Y 2055C>T BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y706Y 2118C>T BTCA-JP X 153175663 153175663 single base substitution G A synonymous_variant Y746Y 2238C>T BTCA-JP X 153175663 153175663 single base substitution G A upstream_gene_variant BTCA-JP X 153184271 153184271 deletion of <=200bp G - downstream_gene_variant BTCA-JP X 153184271 153184271 deletion of <=200bp G - intron_variant BTCA-JP X 153184271 153184271 deletion of <=200bp G - upstream_gene_variant BTCA-JP X 153191680 153191680 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BTCA-JP X 153191680 153191680 single base substitution G A exon_variant BTCA-JP X 153191680 153191680 single base substitution G A intron_variant BTCA-JP X 153191680 153191680 single base substitution G A upstream_gene_variant BTCA-JP X 153195508 153195508 single base substitution C T intron_variant BTCA-JP X 153195508 153195508 single base substitution C T upstream_gene_variant CESC-US X 153171491 153171491 single base substitution C G downstream_gene_variant CESC-US X 153172076 153172076 single base substitution G A downstream_gene_variant CESC-US X 153176375 153176375 single base substitution C G downstream_gene_variant CESC-US X 153176375 153176375 single base substitution C G intron_variant CESC-US X 153176375 153176375 single base substitution C G splice_donor_variant CESC-US X 153176375 153176375 single base substitution C G upstream_gene_variant CESC-US X 153176611 153176611 single base substitution C G 3_prime_UTR_variant CESC-US X 153176611 153176611 single base substitution C G downstream_gene_variant CESC-US X 153176611 153176611 single base substitution C G exon_variant CESC-US X 153176611 153176611 single base substitution C G missense_variant E347D 1041G>C CESC-US X 153176611 153176611 single base substitution C G missense_variant E39D 117G>C CESC-US X 153176611 153176611 single base substitution C G missense_variant E502D 1506G>C CESC-US X 153176611 153176611 single base substitution C G missense_variant E504D 1512G>C CESC-US X 153176611 153176611 single base substitution C G missense_variant E525D 1575G>C CESC-US X 153176611 153176611 single base substitution C G missense_variant E565D 1695G>C CESC-US X 153176611 153176611 single base substitution C G upstream_gene_variant CESC-US X 153178166 153178166 single base substitution C G 3_prime_UTR_variant CESC-US X 153178166 153178166 single base substitution C G downstream_gene_variant CESC-US X 153178166 153178166 single base substitution C G exon_variant CESC-US X 153178166 153178166 single base substitution C G missense_variant E24D 72G>C CESC-US X 153178166 153178166 single base substitution C G missense_variant E332D 996G>C CESC-US X 153178166 153178166 single base substitution C G missense_variant E487D 1461G>C CESC-US X 153178166 153178166 single base substitution C G missense_variant E489D 1467G>C CESC-US X 153178166 153178166 single base substitution C G missense_variant E510D 1530G>C CESC-US X 153178166 153178166 single base substitution C G missense_variant E550D 1650G>C CESC-US X 153178166 153178166 single base substitution C G upstream_gene_variant CESC-US X 153186187 153186187 single base substitution C A downstream_gene_variant CESC-US X 153186187 153186187 single base substitution C A exon_variant CESC-US X 153186187 153186187 single base substitution C A intron_variant CESC-US X 153186187 153186187 single base substitution C A stop_gained E169* 505G>T CESC-US X 153186187 153186187 single base substitution C A stop_gained E171* 511G>T CESC-US X 153186187 153186187 single base substitution C A stop_gained E192* 574G>T CESC-US X 153186187 153186187 single base substitution C A stop_gained E39* 115G>T CESC-US X 153186187 153186187 single base substitution C A upstream_gene_variant CESC-US X 153186238 153186238 single base substitution G C exon_variant CESC-US X 153186238 153186238 single base substitution G C intron_variant CESC-US X 153186238 153186238 single base substitution G C missense_variant H152D 454C>G CESC-US X 153186238 153186238 single base substitution G C missense_variant H154D 460C>G CESC-US X 153186238 153186238 single base substitution G C missense_variant H175D 523C>G CESC-US X 153186238 153186238 single base substitution G C missense_variant H22D 64C>G CESC-US X 153186238 153186238 single base substitution G C upstream_gene_variant CESC-US X 153187188 153187188 single base substitution C G exon_variant CESC-US X 153187188 153187188 single base substitution C G missense_variant E25Q 73G>C CESC-US X 153187188 153187188 single base substitution C G missense_variant E48Q 142G>C CESC-US X 153187188 153187188 single base substitution C G upstream_gene_variant CLLE-ES X 153176687 153176687 single base substitution C A downstream_gene_variant CLLE-ES X 153176687 153176687 single base substitution C A intron_variant CLLE-ES X 153176687 153176687 single base substitution C A upstream_gene_variant CLLE-ES X 153193836 153193836 single base substitution G C 5_prime_UTR_variant CLLE-ES X 153193836 153193836 single base substitution G C intron_variant CLLE-ES X 153193836 153193836 single base substitution G C upstream_gene_variant CLLE-ES X 153204237 153204237 single base substitution T C upstream_gene_variant CLLE-ES X 153204251 153204251 single base substitution T C upstream_gene_variant COAD-US X 153171550 153171550 single base substitution C T downstream_gene_variant COAD-US X 153171551 153171551 single base substitution G A downstream_gene_variant COAD-US X 153172055 153172055 single base substitution G A downstream_gene_variant COAD-US X 153175289 153175289 single base substitution G A 3_prime_UTR_variant COAD-US X 153175289 153175289 single base substitution G A downstream_gene_variant COAD-US X 153175289 153175289 single base substitution G A exon_variant COAD-US X 153175289 153175289 single base substitution G A missense_variant R195W 583C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R262W 784C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R596W 1786C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R751W 2251C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R753W 2257C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R774W 2320C>T COAD-US X 153175289 153175289 single base substitution G A missense_variant R814W 2440C>T COAD-US X 153175289 153175289 single base substitution G A upstream_gene_variant COAD-US X 153175378 153175378 single base substitution T C downstream_gene_variant COAD-US X 153175378 153175378 single base substitution T C missense_variant D165G 494A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D232G 695A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D566G 1697A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D721G 2162A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D723G 2168A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D744G 2231A>G COAD-US X 153175378 153175378 single base substitution T C missense_variant D784G 2351A>G COAD-US X 153175378 153175378 single base substitution T C splice_region_variant COAD-US X 153175378 153175378 single base substitution T C upstream_gene_variant COAD-US X 153175663 153175663 single base substitution G A 3_prime_UTR_variant COAD-US X 153175663 153175663 single base substitution G A downstream_gene_variant COAD-US X 153175663 153175663 single base substitution G A exon_variant COAD-US X 153175663 153175663 single base substitution G A intron_variant COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y194Y 582C>T COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y528Y 1584C>T COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y683Y 2049C>T COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y685Y 2055C>T COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y706Y 2118C>T COAD-US X 153175663 153175663 single base substitution G A synonymous_variant Y746Y 2238C>T COAD-US X 153175663 153175663 single base substitution G A upstream_gene_variant COAD-US X 153178222 153178222 single base substitution G A 3_prime_UTR_variant COAD-US X 153178222 153178222 single base substitution G A downstream_gene_variant COAD-US X 153178222 153178222 single base substitution G A exon_variant COAD-US X 153178222 153178222 single base substitution G A missense_variant R314C 940C>T COAD-US X 153178222 153178222 single base substitution G A missense_variant R469C 1405C>T COAD-US X 153178222 153178222 single base substitution G A missense_variant R471C 1411C>T COAD-US X 153178222 153178222 single base substitution G A missense_variant R492C 1474C>T COAD-US X 153178222 153178222 single base substitution G A missense_variant R532C 1594C>T COAD-US X 153178222 153178222 single base substitution G A missense_variant R6C 16C>T COAD-US X 153178222 153178222 single base substitution G A upstream_gene_variant COAD-US X 153178995 153178995 single base substitution G A 3_prime_UTR_variant COAD-US X 153178995 153178995 single base substitution G A exon_variant COAD-US X 153178995 153178995 single base substitution G A intron_variant COAD-US X 153178995 153178995 single base substitution G A synonymous_variant D220D 660C>T COAD-US X 153178995 153178995 single base substitution G A synonymous_variant D375D 1125C>T COAD-US X 153178995 153178995 single base substitution G A synonymous_variant D377D 1131C>T COAD-US X 153178995 153178995 single base substitution G A synonymous_variant D398D 1194C>T COAD-US X 153178995 153178995 single base substitution G A synonymous_variant D438D 1314C>T COAD-US X 153178995 153178995 single base substitution G A upstream_gene_variant COAD-US X 153185114 153185114 single base substitution G A downstream_gene_variant COAD-US X 153185114 153185114 single base substitution G A intron_variant COAD-US X 153185114 153185114 single base substitution G A synonymous_variant A236A 708C>T COAD-US X 153185114 153185114 single base substitution G A synonymous_variant A83A 249C>T COAD-US X 153187059 153187059 single base substitution G A missense_variant R68W 202C>T COAD-US X 153187059 153187059 single base substitution G A missense_variant R91W 271C>T COAD-US X 153187059 153187059 single base substitution G A splice_region_variant COAD-US X 153187059 153187059 single base substitution G A upstream_gene_variant COAD-US X 153187088 153187088 single base substitution A G exon_variant COAD-US X 153187088 153187088 single base substitution A G missense_variant L58P 173T>C COAD-US X 153187088 153187088 single base substitution A G missense_variant L81P 242T>C COAD-US X 153187088 153187088 single base substitution A G upstream_gene_variant COAD-US X 153197862 153197862 single base substitution C T exon_variant COAD-US X 153197862 153197862 single base substitution C T upstream_gene_variant COCA-CN X 153171451 153171451 single base substitution G T downstream_gene_variant COCA-CN X 153174571 153174571 single base substitution G A 3_prime_UTR_variant COCA-CN X 153174571 153174571 single base substitution G A downstream_gene_variant COCA-CN X 153174571 153174571 single base substitution G A exon_variant COCA-CN X 153174571 153174571 single base substitution G A missense_variant R676C 2026C>T COCA-CN X 153174571 153174571 single base substitution G A missense_variant R831C 2491C>T COCA-CN X 153174571 153174571 single base substitution G A missense_variant R833C 2497C>T COCA-CN X 153174571 153174571 single base substitution G A missense_variant R854C 2560C>T COCA-CN X 153174571 153174571 single base substitution G A missense_variant R894C 2680C>T COCA-CN X 153174870 153174870 single base substitution C G downstream_gene_variant COCA-CN X 153174870 153174870 single base substitution C G intron_variant COCA-CN X 153175016 153175016 single base substitution C T downstream_gene_variant COCA-CN X 153175016 153175016 single base substitution C T exon_variant COCA-CN X 153175016 153175016 single base substitution C T intron_variant COCA-CN X 153175899 153175899 single base substitution C T downstream_gene_variant COCA-CN X 153175899 153175899 single base substitution C T exon_variant COCA-CN X 153175899 153175899 single base substitution C T intron_variant COCA-CN X 153175899 153175899 single base substitution C T upstream_gene_variant COCA-CN X 153176479 153176479 single base substitution G A downstream_gene_variant COCA-CN X 153176479 153176479 single base substitution G A intron_variant COCA-CN X 153176479 153176479 single base substitution G A synonymous_variant C25C 75C>T COCA-CN X 153176479 153176479 single base substitution G A upstream_gene_variant COCA-CN X 153179263 153179263 single base substitution C T 3_prime_UTR_variant COCA-CN X 153179263 153179263 single base substitution C T exon_variant COCA-CN X 153179263 153179263 single base substitution C T missense_variant R143H 428G>A COCA-CN X 153179263 153179263 single base substitution C T missense_variant R190H 569G>A COCA-CN X 153179263 153179263 single base substitution C T missense_variant R345H 1034G>A COCA-CN X 153179263 153179263 single base substitution C T missense_variant R347H 1040G>A COCA-CN X 153179263 153179263 single base substitution C T missense_variant R368H 1103G>A COCA-CN X 153179263 153179263 single base substitution C T missense_variant R408H 1223G>A COCA-CN X 153179263 153179263 single base substitution C T upstream_gene_variant COCA-CN X 153179318 153179318 single base substitution C T 3_prime_UTR_variant COCA-CN X 153179318 153179318 single base substitution C T downstream_gene_variant COCA-CN X 153179318 153179318 single base substitution C T exon_variant COCA-CN X 153179318 153179318 single base substitution C T missense_variant V125I 373G>A COCA-CN X 153179318 153179318 single base substitution C T missense_variant V172I 514G>A COCA-CN X 153179318 153179318 single base substitution C T missense_variant V327I 979G>A COCA-CN X 153179318 153179318 single base substitution C T missense_variant V329I 985G>A COCA-CN X 153179318 153179318 single base substitution C T missense_variant V350I 1048G>A COCA-CN X 153179318 153179318 single base substitution C T missense_variant V390I 1168G>A COCA-CN X 153179318 153179318 single base substitution C T upstream_gene_variant COCA-CN X 153186304 153186304 single base substitution C T intron_variant COCA-CN X 153186304 153186304 single base substitution C T upstream_gene_variant COCA-CN X 153187166 153187166 single base substitution C T exon_variant COCA-CN X 153187166 153187166 single base substitution C T missense_variant R32H 95G>A COCA-CN X 153187166 153187166 single base substitution C T missense_variant R55H 164G>A COCA-CN X 153187166 153187166 single base substitution C T upstream_gene_variant COCA-CN X 153199890 153199890 single base substitution G C exon_variant ESCA-CN X 153171345 153171345 single base substitution A G downstream_gene_variant ESCA-CN X 153175692 153175692 single base substitution G A 3_prime_UTR_variant ESCA-CN X 153175692 153175692 single base substitution G A downstream_gene_variant ESCA-CN X 153175692 153175692 single base substitution G A exon_variant ESCA-CN X 153175692 153175692 single base substitution G A intron_variant ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P185S 553C>T ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P519S 1555C>T ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P674S 2020C>T ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P676S 2026C>T ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P697S 2089C>T ESCA-CN X 153175692 153175692 single base substitution G A missense_variant P737S 2209C>T ESCA-CN X 153175692 153175692 single base substitution G A upstream_gene_variant ESCA-CN X 153179237 153179237 single base substitution C G 3_prime_UTR_variant ESCA-CN X 153179237 153179237 single base substitution C G exon_variant ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E152Q 454G>C ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E199Q 595G>C ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E354Q 1060G>C ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E356Q 1066G>C ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E377Q 1129G>C ESCA-CN X 153179237 153179237 single base substitution C G missense_variant E417Q 1249G>C ESCA-CN X 153179237 153179237 single base substitution C G upstream_gene_variant ESCA-CN X 153184468 153184468 single base substitution G A 3_prime_UTR_variant ESCA-CN X 153184468 153184468 single base substitution G A downstream_gene_variant ESCA-CN X 153184468 153184468 single base substitution G A exon_variant ESCA-CN X 153184468 153184468 single base substitution G A intron_variant ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L171F 511C>T ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L261F 781C>T ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L263F 787C>T ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L284F 850C>T ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L324F 970C>T ESCA-CN X 153184468 153184468 single base substitution G A missense_variant L59F 175C>T ESCA-CN X 153184468 153184468 single base substitution G A upstream_gene_variant ESCA-CN X 153185246 153185246 single base substitution A T downstream_gene_variant ESCA-CN X 153185246 153185246 single base substitution A T intron_variant GBM-US X 153171843 153171843 single base substitution G A downstream_gene_variant GBM-US X 153175809 153175809 single base substitution C T 3_prime_UTR_variant GBM-US X 153175809 153175809 single base substitution C T downstream_gene_variant GBM-US X 153175809 153175809 single base substitution C T exon_variant GBM-US X 153175809 153175809 single base substitution C T intron_variant GBM-US X 153175809 153175809 single base substitution C T missense_variant V146M 436G>A GBM-US X 153175809 153175809 single base substitution C T missense_variant V480M 1438G>A GBM-US X 153175809 153175809 single base substitution C T missense_variant V635M 1903G>A GBM-US X 153175809 153175809 single base substitution C T missense_variant V637M 1909G>A GBM-US X 153175809 153175809 single base substitution C T missense_variant V658M 1972G>A GBM-US X 153175809 153175809 single base substitution C T missense_variant V698M 2092G>A GBM-US X 153175809 153175809 single base substitution C T upstream_gene_variant GBM-US X 153184317 153184317 single base substitution C T 3_prime_UTR_variant GBM-US X 153184317 153184317 single base substitution C T downstream_gene_variant GBM-US X 153184317 153184317 single base substitution C T exon_variant GBM-US X 153184317 153184317 single base substitution C T intron_variant GBM-US X 153184317 153184317 single base substitution C T missense_variant R109H 326G>A GBM-US X 153184317 153184317 single base substitution C T missense_variant R311H 932G>A GBM-US X 153184317 153184317 single base substitution C T missense_variant R313H 938G>A GBM-US X 153184317 153184317 single base substitution C T missense_variant R334H 1001G>A GBM-US X 153184317 153184317 single base substitution C T missense_variant R374H 1121G>A GBM-US X 153184317 153184317 single base substitution C T upstream_gene_variant KIRC-US X 153170604 153170604 single base substitution T C downstream_gene_variant KIRC-US X 153171715 153171715 single base substitution G A downstream_gene_variant KIRC-US X 153196257 153196257 single base substitution C T intron_variant KIRC-US X 153196257 153196257 single base substitution C T upstream_gene_variant KIRP-US X 153171162 153171162 insertion of <=200bp - G downstream_gene_variant KIRP-US X 153198018 153198018 single base substitution C T exon_variant KIRP-US X 153198018 153198018 single base substitution C T upstream_gene_variant KIRP-US X 153200984 153200984 insertion of <=200bp - T upstream_gene_variant LAML-KR X 153176730 153176730 single base substitution G T downstream_gene_variant LAML-KR X 153176730 153176730 single base substitution G T intron_variant LAML-KR X 153176730 153176730 single base substitution G T upstream_gene_variant LAML-KR X 153178313 153178313 single base substitution A C downstream_gene_variant LAML-KR X 153178313 153178313 single base substitution A C intron_variant LAML-KR X 153178313 153178313 single base substitution A C upstream_gene_variant LGG-US X 153172155 153172155 single base substitution C T downstream_gene_variant LGG-US X 153175536 153175536 single base substitution G A 3_prime_UTR_variant LGG-US X 153175536 153175536 single base substitution G A downstream_gene_variant LGG-US X 153175536 153175536 single base substitution G A exon_variant LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D141D 423C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D208D 624C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D542D 1626C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D697D 2091C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D699D 2097C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D720D 2160C>T LGG-US X 153175536 153175536 single base substitution G A synonymous_variant D760D 2280C>T LGG-US X 153175536 153175536 single base substitution G A upstream_gene_variant LGG-US X 153195525 153195525 single base substitution T C intron_variant LGG-US X 153195525 153195525 single base substitution T C upstream_gene_variant LGG-US X 153195616 153195616 single base substitution T C intron_variant LGG-US X 153195616 153195616 single base substitution T C upstream_gene_variant LICA-CN X 153175523 153175523 single base substitution T A 3_prime_UTR_variant LICA-CN X 153175523 153175523 single base substitution T A downstream_gene_variant LICA-CN X 153175523 153175523 single base substitution T A exon_variant LICA-CN X 153175523 153175523 single base substitution T A missense_variant S146C 436A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S213C 637A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S547C 1639A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S702C 2104A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S704C 2110A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S725C 2173A>T LICA-CN X 153175523 153175523 single base substitution T A missense_variant S765C 2293A>T LICA-CN X 153175523 153175523 single base substitution T A upstream_gene_variant LICA-FR X 153168573 153168573 single base substitution C A downstream_gene_variant LICA-FR X 153178727 153178727 single base substitution G A 3_prime_UTR_variant LICA-FR X 153178727 153178727 single base substitution G A downstream_gene_variant LICA-FR X 153178727 153178727 single base substitution G A exon_variant LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S199S 597C>T LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S274S 822C>T LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S429S 1287C>T LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S431S 1293C>T LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S452S 1356C>T LICA-FR X 153178727 153178727 single base substitution G A synonymous_variant S492S 1476C>T LICA-FR X 153178727 153178727 single base substitution G A upstream_gene_variant LICA-FR X 153186166 153186166 single base substitution T A downstream_gene_variant LICA-FR X 153186166 153186166 single base substitution T A exon_variant LICA-FR X 153186166 153186166 single base substitution T A intron_variant LICA-FR X 153186166 153186166 single base substitution T A missense_variant S176C 526A>T LICA-FR X 153186166 153186166 single base substitution T A missense_variant S178C 532A>T LICA-FR X 153186166 153186166 single base substitution T A missense_variant S199C 595A>T LICA-FR X 153186166 153186166 single base substitution T A missense_variant S46C 136A>T LICA-FR X 153186166 153186166 single base substitution T A upstream_gene_variant LICA-FR X 153186860 153186860 single base substitution G A exon_variant LICA-FR X 153186860 153186860 single base substitution G A synonymous_variant R108R 324C>T LICA-FR X 153186860 153186860 single base substitution G A synonymous_variant R131R 393C>T LICA-FR X 153186860 153186860 single base substitution G A upstream_gene_variant LICA-FR X 153187693 153187693 single base substitution A T 5_prime_UTR_variant LICA-FR X 153187693 153187693 single base substitution A T intron_variant LICA-FR X 153187693 153187693 single base substitution A T upstream_gene_variant LICA-FR X 153200970 153200970 single base substitution G A upstream_gene_variant LIHC-US X 153185069 153185069 single base substitution G T downstream_gene_variant LIHC-US X 153185069 153185069 single base substitution G T intron_variant LIHC-US X 153185069 153185069 single base substitution G T synonymous_variant L251L 753C>A LIHC-US X 153185069 153185069 single base substitution G T synonymous_variant L98L 294C>A LINC-JP X 153171401 153171401 single base substitution G A downstream_gene_variant LINC-JP X 153173475 153173475 single base substitution A G downstream_gene_variant LINC-JP X 153173475 153173475 single base substitution A G intron_variant LINC-JP X 153176839 153176839 single base substitution A G downstream_gene_variant LINC-JP X 153176839 153176839 single base substitution A G intron_variant LINC-JP X 153176839 153176839 single base substitution A G upstream_gene_variant LINC-JP X 153178865 153178865 single base substitution T C downstream_gene_variant LINC-JP X 153178865 153178865 single base substitution T C exon_variant LINC-JP X 153178865 153178865 single base substitution T C missense_variant T189A 565A>G LINC-JP X 153178865 153178865 single base substitution T C missense_variant T264A 790A>G LINC-JP X 153178865 153178865 single base substitution T C missense_variant T419A 1255A>G LINC-JP X 153178865 153178865 single base substitution T C missense_variant T421A 1261A>G LINC-JP X 153178865 153178865 single base substitution T C missense_variant T442A 1324A>G LINC-JP X 153178865 153178865 single base substitution T C missense_variant T482A 1444A>G LINC-JP X 153178865 153178865 single base substitution T C splice_region_variant LINC-JP X 153178865 153178865 single base substitution T C upstream_gene_variant LINC-JP X 153186793 153186793 single base substitution C A intron_variant LINC-JP X 153186793 153186793 single base substitution C A upstream_gene_variant LINC-JP X 153191701 153191701 single base substitution G T 5_prime_UTR_variant LINC-JP X 153191701 153191701 single base substitution G T intron_variant LINC-JP X 153191701 153191701 single base substitution G T upstream_gene_variant LIRI-JP X 153167860 153167860 single base substitution G T downstream_gene_variant LIRI-JP X 153184593 153184593 single base substitution C T downstream_gene_variant LIRI-JP X 153184593 153184593 single base substitution C T intron_variant LIRI-JP X 153184593 153184593 single base substitution C T upstream_gene_variant LIRI-JP X 153187251 153187251 single base substitution G A exon_variant LIRI-JP X 153187251 153187251 single base substitution G A stop_gained Q27* 79C>T LIRI-JP X 153187251 153187251 single base substitution G A stop_gained Q4* 10C>T LIRI-JP X 153187251 153187251 single base substitution G A upstream_gene_variant LIRI-JP X 153187257 153187257 single base substitution G A exon_variant LIRI-JP X 153187257 153187257 single base substitution G A missense_variant R25C 73C>T LIRI-JP X 153187257 153187257 single base substitution G A missense_variant R2C 4C>T LIRI-JP X 153187257 153187257 single base substitution G A upstream_gene_variant LIRI-JP X 153191892 153191892 single base substitution C G intron_variant LIRI-JP X 153191892 153191892 single base substitution C G upstream_gene_variant LIRI-JP X 153194421 153194421 single base substitution T A intron_variant LIRI-JP X 153194421 153194421 single base substitution T A upstream_gene_variant LIRI-JP X 153194619 153194619 single base substitution T C intron_variant LIRI-JP X 153194619 153194619 single base substitution T C upstream_gene_variant LIRI-JP X 153198837 153198837 single base substitution T C intron_variant LIRI-JP X 153198837 153198837 single base substitution T C upstream_gene_variant LIRI-JP X 153202536 153202536 single base substitution C A upstream_gene_variant LUSC-KR X 153168154 153168154 single base substitution G A downstream_gene_variant LUSC-KR X 153169322 153169322 single base substitution G T downstream_gene_variant LUSC-KR X 153169645 153169645 single base substitution C A downstream_gene_variant LUSC-KR X 153170355 153170355 single base substitution A C downstream_gene_variant LUSC-KR X 153172059 153172059 single base substitution C T downstream_gene_variant LUSC-KR X 153172659 153172659 single base substitution T C downstream_gene_variant LUSC-KR X 153175586 153175586 single base substitution G C downstream_gene_variant LUSC-KR X 153175586 153175586 single base substitution G C exon_variant LUSC-KR X 153175586 153175586 single base substitution G C intron_variant LUSC-KR X 153175586 153175586 single base substitution G C upstream_gene_variant LUSC-KR X 153179706 153179706 single base substitution C G downstream_gene_variant LUSC-KR X 153179706 153179706 single base substitution C G exon_variant LUSC-KR X 153179706 153179706 single base substitution C G intron_variant LUSC-KR X 153179706 153179706 single base substitution C G upstream_gene_variant LUSC-KR X 153195393 153195393 single base substitution G A intron_variant LUSC-KR X 153195393 153195393 single base substitution G A upstream_gene_variant LUSC-KR X 153197461 153197461 single base substitution G C intron_variant LUSC-KR X 153197461 153197461 single base substitution G C upstream_gene_variant LUSC-KR X 153197480 153197480 single base substitution C A intron_variant LUSC-KR X 153197480 153197480 single base substitution C A upstream_gene_variant LUSC-US X 153171312 153171312 single base substitution C A downstream_gene_variant LUSC-US X 153171711 153171711 single base substitution C A downstream_gene_variant LUSC-US X 153171764 153171764 single base substitution G C downstream_gene_variant LUSC-US X 153173229 153173229 single base substitution G C 3_prime_UTR_variant LUSC-US X 153173229 153173229 single base substitution G C downstream_gene_variant LUSC-US X 153173229 153173229 single base substitution G C exon_variant LUSC-US X 153173229 153173229 single base substitution G C stop_gained S754* 2261C>G LUSC-US X 153173229 153173229 single base substitution G C stop_gained S909* 2726C>G LUSC-US X 153173229 153173229 single base substitution G C stop_gained S911* 2732C>G LUSC-US X 153173229 153173229 single base substitution G C stop_gained S932* 2795C>G LUSC-US X 153173229 153173229 single base substitution G C stop_gained S972* 2915C>G LUSC-US X 153173337 153173337 single base substitution G C 3_prime_UTR_variant LUSC-US X 153173337 153173337 single base substitution G C downstream_gene_variant LUSC-US X 153173337 153173337 single base substitution G C exon_variant LUSC-US X 153173337 153173337 single base substitution G C missense_variant S718C 2153C>G LUSC-US X 153173337 153173337 single base substitution G C missense_variant S873C 2618C>G LUSC-US X 153173337 153173337 single base substitution G C missense_variant S875C 2624C>G LUSC-US X 153173337 153173337 single base substitution G C missense_variant S896C 2687C>G LUSC-US X 153173337 153173337 single base substitution G C missense_variant S936C 2807C>G LUSC-US X 153195481 153195481 single base substitution C G intron_variant LUSC-US X 153195481 153195481 single base substitution C G upstream_gene_variant LUSC-US X 153195637 153195637 single base substitution C T intron_variant LUSC-US X 153195637 153195637 single base substitution C T upstream_gene_variant MALY-DE X 153193064 153193064 single base substitution G C intron_variant MALY-DE X 153193064 153193064 single base substitution G C upstream_gene_variant MALY-DE X 153200899 153200899 single base substitution C A upstream_gene_variant MALY-DE X 153201681 153201681 single base substitution C T upstream_gene_variant MALY-DE X 153205450 153205450 single base substitution A G upstream_gene_variant MELA-AU X 153167893 153167893 single base substitution C T downstream_gene_variant MELA-AU X 153168027 153168027 single base substitution C T downstream_gene_variant MELA-AU X 153168052 153168052 single base substitution C T downstream_gene_variant MELA-AU X 153168988 153168988 single base substitution G A downstream_gene_variant MELA-AU X 153169362 153169362 single base substitution G A downstream_gene_variant MELA-AU X 153169824 153169824 single base substitution G A downstream_gene_variant MELA-AU X 153169832 153169832 single base substitution C T downstream_gene_variant MELA-AU X 153169983 153169983 single base substitution G A downstream_gene_variant MELA-AU X 153170005 153170005 single base substitution G A downstream_gene_variant MELA-AU X 153170299 153170299 single base substitution G A downstream_gene_variant MELA-AU X 153170671 153170671 single base substitution G A downstream_gene_variant MELA-AU X 153171290 153171290 single base substitution C T downstream_gene_variant MELA-AU X 153171602 153171602 single base substitution C T downstream_gene_variant MELA-AU X 153171651 153171651 single base substitution G A downstream_gene_variant MELA-AU X 153172522 153172522 single base substitution G A downstream_gene_variant MELA-AU X 153172616 153172616 single base substitution C T downstream_gene_variant MELA-AU X 153173255 153173255 single base substitution C T 3_prime_UTR_variant MELA-AU X 153173255 153173255 single base substitution C T downstream_gene_variant MELA-AU X 153173255 153173255 single base substitution C T exon_variant MELA-AU X 153173255 153173255 single base substitution C T synonymous_variant R745R 2235G>A MELA-AU X 153173255 153173255 single base substitution C T synonymous_variant R900R 2700G>A MELA-AU X 153173255 153173255 single base substitution C T synonymous_variant R902R 2706G>A MELA-AU X 153173255 153173255 single base substitution C T synonymous_variant R923R 2769G>A MELA-AU X 153173255 153173255 single base substitution C T synonymous_variant R963R 2889G>A MELA-AU X 153173543 153173543 single base substitution C T downstream_gene_variant MELA-AU X 153173543 153173543 single base substitution C T intron_variant MELA-AU X 153173717 153173718 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 153173717 153173718 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 153174083 153174083 single base substitution C T downstream_gene_variant MELA-AU X 153174083 153174083 single base substitution C T intron_variant MELA-AU X 153174205 153174205 single base substitution G A downstream_gene_variant MELA-AU X 153174205 153174205 single base substitution G A intron_variant MELA-AU X 153175167 153175167 single base substitution C T downstream_gene_variant MELA-AU X 153175167 153175167 single base substitution C T intron_variant MELA-AU X 153175167 153175167 single base substitution C T upstream_gene_variant MELA-AU X 153175741 153175741 single base substitution C T 3_prime_UTR_variant MELA-AU X 153175741 153175741 single base substitution C T downstream_gene_variant MELA-AU X 153175741 153175741 single base substitution C T exon_variant MELA-AU X 153175741 153175741 single base substitution C T intron_variant MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V168V 504G>A MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V502V 1506G>A MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V657V 1971G>A MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V659V 1977G>A MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V680V 2040G>A MELA-AU X 153175741 153175741 single base substitution C T synonymous_variant V720V 2160G>A MELA-AU X 153175741 153175741 single base substitution C T upstream_gene_variant MELA-AU X 153176327 153176327 single base substitution G A downstream_gene_variant MELA-AU X 153176327 153176327 single base substitution G A intron_variant MELA-AU X 153176327 153176327 single base substitution G A upstream_gene_variant MELA-AU X 153176915 153176915 single base substitution C T downstream_gene_variant MELA-AU X 153176915 153176915 single base substitution C T intron_variant MELA-AU X 153176915 153176915 single base substitution C T upstream_gene_variant MELA-AU X 153177307 153177307 single base substitution G A downstream_gene_variant MELA-AU X 153177307 153177307 single base substitution G A intron_variant MELA-AU X 153177307 153177307 single base substitution G A upstream_gene_variant MELA-AU X 153177471 153177471 single base substitution G A downstream_gene_variant MELA-AU X 153177471 153177471 single base substitution G A intron_variant MELA-AU X 153177471 153177471 single base substitution G A upstream_gene_variant MELA-AU X 153177557 153177557 single base substitution C T downstream_gene_variant MELA-AU X 153177557 153177557 single base substitution C T intron_variant MELA-AU X 153177557 153177557 single base substitution C T upstream_gene_variant MELA-AU X 153177714 153177714 single base substitution G A downstream_gene_variant MELA-AU X 153177714 153177714 single base substitution G A intron_variant MELA-AU X 153177714 153177714 single base substitution G A upstream_gene_variant MELA-AU X 153177899 153177899 single base substitution C T downstream_gene_variant MELA-AU X 153177899 153177899 single base substitution C T intron_variant MELA-AU X 153177899 153177899 single base substitution C T upstream_gene_variant MELA-AU X 153178382 153178382 single base substitution G A downstream_gene_variant MELA-AU X 153178382 153178382 single base substitution G A intron_variant MELA-AU X 153178382 153178382 single base substitution G A upstream_gene_variant MELA-AU X 153178568 153178568 single base substitution G A downstream_gene_variant MELA-AU X 153178568 153178568 single base substitution G A intron_variant MELA-AU X 153178568 153178568 single base substitution G A upstream_gene_variant MELA-AU X 153178604 153178604 single base substitution G A downstream_gene_variant MELA-AU X 153178604 153178604 single base substitution G A intron_variant MELA-AU X 153178604 153178604 single base substitution G A upstream_gene_variant MELA-AU X 153178624 153178624 single base substitution G A downstream_gene_variant MELA-AU X 153178624 153178624 single base substitution G A intron_variant MELA-AU X 153178624 153178624 single base substitution G A upstream_gene_variant MELA-AU X 153178654 153178654 single base substitution G A downstream_gene_variant MELA-AU X 153178654 153178654 single base substitution G A intron_variant MELA-AU X 153178654 153178654 single base substitution G A upstream_gene_variant MELA-AU X 153178721 153178721 single base substitution G A 3_prime_UTR_variant MELA-AU X 153178721 153178721 single base substitution G A downstream_gene_variant MELA-AU X 153178721 153178721 single base substitution G A exon_variant MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L201L 603C>T MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L276L 828C>T MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L431L 1293C>T MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L433L 1299C>T MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L454L 1362C>T MELA-AU X 153178721 153178721 single base substitution G A synonymous_variant L494L 1482C>T MELA-AU X 153178721 153178721 single base substitution G A upstream_gene_variant MELA-AU X 153178881 153178881 single base substitution G C 3_prime_UTR_variant MELA-AU X 153178881 153178881 single base substitution G C downstream_gene_variant MELA-AU X 153178881 153178881 single base substitution G C exon_variant MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T183T 549C>G MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T258T 774C>G MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T413T 1239C>G MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T415T 1245C>G MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T436T 1308C>G MELA-AU X 153178881 153178881 single base substitution G C synonymous_variant T476T 1428C>G MELA-AU X 153178881 153178881 single base substitution G C upstream_gene_variant MELA-AU X 153179721 153179721 single base substitution G A downstream_gene_variant MELA-AU X 153179721 153179721 single base substitution G A intron_variant MELA-AU X 153179721 153179721 single base substitution G A upstream_gene_variant MELA-AU X 153180287 153180287 single base substitution C T downstream_gene_variant MELA-AU X 153180287 153180287 single base substitution C T intron_variant MELA-AU X 153180287 153180287 single base substitution C T upstream_gene_variant MELA-AU X 153180819 153180819 single base substitution G A downstream_gene_variant MELA-AU X 153180819 153180819 single base substitution G A intron_variant MELA-AU X 153180819 153180819 single base substitution G A upstream_gene_variant MELA-AU X 153181053 153181053 single base substitution A G downstream_gene_variant MELA-AU X 153181053 153181053 single base substitution A G intron_variant MELA-AU X 153181053 153181053 single base substitution A G upstream_gene_variant MELA-AU X 153181266 153181266 single base substitution C T downstream_gene_variant MELA-AU X 153181266 153181266 single base substitution C T intron_variant MELA-AU X 153181266 153181266 single base substitution C T upstream_gene_variant MELA-AU X 153181543 153181543 single base substitution G A downstream_gene_variant MELA-AU X 153181543 153181543 single base substitution G A intron_variant MELA-AU X 153181543 153181543 single base substitution G A upstream_gene_variant MELA-AU X 153181681 153181681 single base substitution G A downstream_gene_variant MELA-AU X 153181681 153181681 single base substitution G A intron_variant MELA-AU X 153181681 153181681 single base substitution G A upstream_gene_variant MELA-AU X 153181744 153181744 single base substitution G A downstream_gene_variant MELA-AU X 153181744 153181744 single base substitution G A intron_variant MELA-AU X 153181744 153181744 single base substitution G A upstream_gene_variant MELA-AU X 153182042 153182042 single base substitution G A downstream_gene_variant MELA-AU X 153182042 153182042 single base substitution G A intron_variant MELA-AU X 153182042 153182042 single base substitution G A upstream_gene_variant MELA-AU X 153182580 153182580 single base substitution G A downstream_gene_variant MELA-AU X 153182580 153182580 single base substitution G A intron_variant MELA-AU X 153182580 153182580 single base substitution G A upstream_gene_variant MELA-AU X 153183093 153183093 single base substitution C T downstream_gene_variant MELA-AU X 153183093 153183093 single base substitution C T intron_variant MELA-AU X 153183093 153183093 single base substitution C T upstream_gene_variant MELA-AU X 153183334 153183334 single base substitution G A downstream_gene_variant MELA-AU X 153183334 153183334 single base substitution G A intron_variant MELA-AU X 153183334 153183334 single base substitution G A upstream_gene_variant MELA-AU X 153183777 153183777 single base substitution G A downstream_gene_variant MELA-AU X 153183777 153183777 single base substitution G A intron_variant MELA-AU X 153183777 153183777 single base substitution G A upstream_gene_variant MELA-AU X 153184179 153184179 single base substitution C T downstream_gene_variant MELA-AU X 153184179 153184179 single base substitution C T intron_variant MELA-AU X 153184179 153184179 single base substitution C T upstream_gene_variant MELA-AU X 153184262 153184262 single base substitution A G downstream_gene_variant MELA-AU X 153184262 153184262 single base substitution A G intron_variant MELA-AU X 153184262 153184262 single base substitution A G upstream_gene_variant MELA-AU X 153186035 153186035 single base substitution G A downstream_gene_variant MELA-AU X 153186035 153186035 single base substitution G A exon_variant MELA-AU X 153186035 153186035 single base substitution G A intron_variant MELA-AU X 153186336 153186336 single base substitution C T intron_variant MELA-AU X 153186336 153186336 single base substitution C T upstream_gene_variant MELA-AU X 153186409 153186409 single base substitution G A intron_variant MELA-AU X 153186409 153186409 single base substitution G A upstream_gene_variant MELA-AU X 153186976 153186977 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU X 153186976 153186977 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant KE69KK MELA-AU X 153186976 153186977 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant KE92KK MELA-AU X 153186976 153186977 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 153186980 153186980 single base substitution C T splice_region_variant MELA-AU X 153186980 153186980 single base substitution C T upstream_gene_variant MELA-AU X 153187510 153187510 single base substitution C T intron_variant MELA-AU X 153187510 153187510 single base substitution C T upstream_gene_variant MELA-AU X 153188172 153188172 single base substitution C T intron_variant MELA-AU X 153188172 153188172 single base substitution C T upstream_gene_variant MELA-AU X 153188414 153188414 single base substitution G A intron_variant MELA-AU X 153188414 153188414 single base substitution G A upstream_gene_variant MELA-AU X 153188546 153188546 single base substitution C T intron_variant MELA-AU X 153188546 153188546 single base substitution C T upstream_gene_variant MELA-AU X 153189054 153189054 single base substitution G A intron_variant MELA-AU X 153189054 153189054 single base substitution G A upstream_gene_variant MELA-AU X 153189059 153189059 single base substitution G A intron_variant MELA-AU X 153189059 153189059 single base substitution G A upstream_gene_variant MELA-AU X 153190349 153190349 single base substitution G A intron_variant MELA-AU X 153190349 153190349 single base substitution G A upstream_gene_variant MELA-AU X 153190909 153190909 single base substitution T C intron_variant MELA-AU X 153190909 153190909 single base substitution T C upstream_gene_variant MELA-AU X 153191271 153191271 single base substitution G A intron_variant MELA-AU X 153191271 153191271 single base substitution G A upstream_gene_variant MELA-AU X 153191682 153191682 single base substitution A G 5_prime_UTR_variant MELA-AU X 153191682 153191682 single base substitution A G exon_variant MELA-AU X 153191682 153191682 single base substitution A G intron_variant MELA-AU X 153191682 153191682 single base substitution A G upstream_gene_variant MELA-AU X 153191694 153191694 single base substitution C T 5_prime_UTR_variant MELA-AU X 153191694 153191694 single base substitution C T exon_variant MELA-AU X 153191694 153191694 single base substitution C T intron_variant MELA-AU X 153191694 153191694 single base substitution C T upstream_gene_variant MELA-AU X 153192207 153192207 single base substitution T G 5_prime_UTR_variant MELA-AU X 153192207 153192207 single base substitution T G intron_variant MELA-AU X 153192207 153192207 single base substitution T G upstream_gene_variant MELA-AU X 153192507 153192507 single base substitution C T intron_variant MELA-AU X 153192507 153192507 single base substitution C T upstream_gene_variant MELA-AU X 153193633 153193633 single base substitution G A intron_variant MELA-AU X 153193633 153193633 single base substitution G A upstream_gene_variant MELA-AU X 153193698 153193698 single base substitution G A intron_variant MELA-AU X 153193698 153193698 single base substitution G A upstream_gene_variant MELA-AU X 153193797 153193797 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU X 153193797 153193797 single base substitution G A exon_variant MELA-AU X 153193797 153193797 single base substitution G A intron_variant MELA-AU X 153193797 153193797 single base substitution G A upstream_gene_variant MELA-AU X 153195204 153195204 single base substitution C T intron_variant MELA-AU X 153195204 153195204 single base substitution C T upstream_gene_variant MELA-AU X 153195884 153195884 single base substitution G A intron_variant MELA-AU X 153195884 153195884 single base substitution G A upstream_gene_variant MELA-AU X 153196096 153196096 single base substitution G A intron_variant MELA-AU X 153196096 153196096 single base substitution G A upstream_gene_variant MELA-AU X 153197870 153197870 single base substitution G A exon_variant MELA-AU X 153197870 153197870 single base substitution G A upstream_gene_variant MELA-AU X 153198701 153198701 single base substitution G A intron_variant MELA-AU X 153198701 153198701 single base substitution G A upstream_gene_variant MELA-AU X 153199814 153199814 single base substitution T A intron_variant MELA-AU X 153199935 153199935 single base substitution G A splice_region_variant MELA-AU X 153201671 153201671 single base substitution A C upstream_gene_variant MELA-AU X 153201780 153201780 single base substitution G A upstream_gene_variant MELA-AU X 153202180 153202180 single base substitution C T upstream_gene_variant MELA-AU X 153202266 153202266 single base substitution C T upstream_gene_variant MELA-AU X 153202717 153202717 single base substitution C T upstream_gene_variant MELA-AU X 153202725 153202725 single base substitution C T upstream_gene_variant MELA-AU X 153202893 153202893 single base substitution G T upstream_gene_variant MELA-AU X 153203399 153203399 single base substitution G A upstream_gene_variant MELA-AU X 153204534 153204534 single base substitution A C upstream_gene_variant ORCA-IN X 153178864 153178864 single base substitution G A downstream_gene_variant ORCA-IN X 153178864 153178864 single base substitution G A exon_variant ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T189M 566C>T ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T264M 791C>T ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T419M 1256C>T ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T421M 1262C>T ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T442M 1325C>T ORCA-IN X 153178864 153178864 single base substitution G A missense_variant T482M 1445C>T ORCA-IN X 153178864 153178864 single base substitution G A splice_region_variant ORCA-IN X 153178864 153178864 single base substitution G A upstream_gene_variant ORCA-IN X 153195620 153195620 single base substitution G C intron_variant ORCA-IN X 153195620 153195620 single base substitution G C upstream_gene_variant OV-AU X 153169514 153169514 single base substitution G T downstream_gene_variant OV-AU X 153173220 153173220 single base substitution T G 3_prime_UTR_variant OV-AU X 153173220 153173220 single base substitution T G downstream_gene_variant OV-AU X 153173220 153173220 single base substitution T G exon_variant OV-AU X 153173220 153173220 single base substitution T G missense_variant H757P 2270A>C OV-AU X 153173220 153173220 single base substitution T G missense_variant H912P 2735A>C OV-AU X 153173220 153173220 single base substitution T G missense_variant H914P 2741A>C OV-AU X 153173220 153173220 single base substitution T G missense_variant H935P 2804A>C OV-AU X 153173220 153173220 single base substitution T G missense_variant H975P 2924A>C OV-AU X 153180821 153180821 single base substitution G A downstream_gene_variant OV-AU X 153180821 153180821 single base substitution G A intron_variant OV-AU X 153180821 153180821 single base substitution G A upstream_gene_variant OV-AU X 153182037 153182037 single base substitution A C downstream_gene_variant OV-AU X 153182037 153182037 single base substitution A C intron_variant OV-AU X 153182037 153182037 single base substitution A C upstream_gene_variant OV-AU X 153183222 153183222 single base substitution A C downstream_gene_variant OV-AU X 153183222 153183222 single base substitution A C intron_variant OV-AU X 153183222 153183222 single base substitution A C upstream_gene_variant OV-AU X 153184779 153184779 single base substitution C A downstream_gene_variant OV-AU X 153184779 153184779 single base substitution C A intron_variant OV-AU X 153186396 153186396 single base substitution C T intron_variant OV-AU X 153186396 153186396 single base substitution C T upstream_gene_variant OV-AU X 153186549 153186549 single base substitution C G intron_variant OV-AU X 153186549 153186549 single base substitution C G splice_donor_variant OV-AU X 153186549 153186549 single base substitution C G upstream_gene_variant OV-AU X 153194291 153194291 single base substitution A T intron_variant OV-AU X 153194291 153194291 single base substitution A T upstream_gene_variant OV-AU X 153200209 153200209 single base substitution G T intron_variant OV-AU X 153200808 153200808 single base substitution G A upstream_gene_variant OV-AU X 153203744 153203744 single base substitution C T upstream_gene_variant OV-AU X 153203811 153203811 single base substitution T A upstream_gene_variant PACA-AU X 153168995 153168995 single base substitution G A downstream_gene_variant PACA-AU X 153174509 153174509 single base substitution C G downstream_gene_variant PACA-AU X 153174509 153174509 single base substitution C G intron_variant PACA-AU X 153179709 153179709 single base substitution G C downstream_gene_variant PACA-AU X 153179709 153179709 single base substitution G C intron_variant PACA-AU X 153179709 153179709 single base substitution G C upstream_gene_variant PACA-AU X 153179716 153179716 single base substitution G A downstream_gene_variant PACA-AU X 153179716 153179716 single base substitution G A intron_variant PACA-AU X 153179716 153179716 single base substitution G A upstream_gene_variant PACA-AU X 153181105 153181105 single base substitution G A downstream_gene_variant PACA-AU X 153181105 153181105 single base substitution G A intron_variant PACA-AU X 153181105 153181105 single base substitution G A upstream_gene_variant PACA-AU X 153182185 153182185 single base substitution G T downstream_gene_variant PACA-AU X 153182185 153182185 single base substitution G T intron_variant PACA-AU X 153182185 153182185 single base substitution G T upstream_gene_variant PACA-AU X 153185325 153185325 single base substitution C T downstream_gene_variant PACA-AU X 153185325 153185325 single base substitution C T intron_variant PACA-AU X 153191836 153191836 single base substitution C A intron_variant PACA-AU X 153191836 153191836 single base substitution C A upstream_gene_variant PACA-AU X 153195389 153195389 single base substitution G A intron_variant PACA-AU X 153195389 153195389 single base substitution G A upstream_gene_variant PACA-AU X 153200225 153200225 single base substitution G A intron_variant PACA-AU X 153201907 153201907 single base substitution C T upstream_gene_variant PACA-AU X 153201908 153201908 single base substitution A G upstream_gene_variant PACA-AU X 153201914 153201914 single base substitution G A upstream_gene_variant PACA-AU X 153202046 153202046 deletion of <=200bp C - upstream_gene_variant PACA-AU X 153202651 153202651 insertion of <=200bp - AAAT upstream_gene_variant PACA-AU X 153202651 153202654 deletion of <=200bp AAAT - upstream_gene_variant PACA-AU X 153203077 153203077 single base substitution T A upstream_gene_variant PACA-AU X 153203850 153203850 single base substitution G A upstream_gene_variant PACA-CA X 153169180 153169180 single base substitution G A downstream_gene_variant PACA-CA X 153171153 153171153 insertion of <=200bp - G downstream_gene_variant PACA-CA X 153171624 153171624 single base substitution G A downstream_gene_variant PACA-CA X 153173957 153173957 single base substitution A T downstream_gene_variant PACA-CA X 153173957 153173957 single base substitution A T intron_variant PACA-CA X 153177635 153177635 single base substitution C T downstream_gene_variant PACA-CA X 153177635 153177635 single base substitution C T intron_variant PACA-CA X 153177635 153177635 single base substitution C T upstream_gene_variant PACA-CA X 153177664 153177664 single base substitution C T downstream_gene_variant PACA-CA X 153177664 153177664 single base substitution C T intron_variant PACA-CA X 153177664 153177664 single base substitution C T upstream_gene_variant PACA-CA X 153177959 153177959 single base substitution C A downstream_gene_variant PACA-CA X 153177959 153177959 single base substitution C A intron_variant PACA-CA X 153177959 153177959 single base substitution C A upstream_gene_variant PACA-CA X 153178153 153178153 single base substitution C T downstream_gene_variant PACA-CA X 153178153 153178153 single base substitution C T splice_donor_variant PACA-CA X 153178153 153178153 single base substitution C T upstream_gene_variant PACA-CA X 153180142 153180142 single base substitution C T downstream_gene_variant PACA-CA X 153180142 153180142 single base substitution C T intron_variant PACA-CA X 153180142 153180142 single base substitution C T upstream_gene_variant PACA-CA X 153182843 153182843 single base substitution G A downstream_gene_variant PACA-CA X 153182843 153182843 single base substitution G A intron_variant PACA-CA X 153182843 153182843 single base substitution G A upstream_gene_variant PACA-CA X 153183340 153183340 single base substitution G C downstream_gene_variant PACA-CA X 153183340 153183340 single base substitution G C intron_variant PACA-CA X 153183340 153183340 single base substitution G C upstream_gene_variant PACA-CA X 153184318 153184318 single base substitution G A 3_prime_UTR_variant PACA-CA X 153184318 153184318 single base substitution G A downstream_gene_variant PACA-CA X 153184318 153184318 single base substitution G A exon_variant PACA-CA X 153184318 153184318 single base substitution G A intron_variant PACA-CA X 153184318 153184318 single base substitution G A missense_variant R109C 325C>T PACA-CA X 153184318 153184318 single base substitution G A missense_variant R311C 931C>T PACA-CA X 153184318 153184318 single base substitution G A missense_variant R313C 937C>T PACA-CA X 153184318 153184318 single base substitution G A missense_variant R334C 1000C>T PACA-CA X 153184318 153184318 single base substitution G A missense_variant R374C 1120C>T PACA-CA X 153184318 153184318 single base substitution G A upstream_gene_variant PACA-CA X 153184758 153184758 single base substitution G A downstream_gene_variant PACA-CA X 153184758 153184758 single base substitution G A intron_variant PACA-CA X 153186697 153186697 insertion of <=200bp - G intron_variant PACA-CA X 153186697 153186697 insertion of <=200bp - G upstream_gene_variant PACA-CA X 153187256 153187256 single base substitution C T exon_variant PACA-CA X 153187256 153187256 single base substitution C T missense_variant R25H 74G>A PACA-CA X 153187256 153187256 single base substitution C T missense_variant R2H 5G>A PACA-CA X 153187256 153187256 single base substitution C T upstream_gene_variant PACA-CA X 153188649 153188649 single base substitution G T intron_variant PACA-CA X 153188649 153188649 single base substitution G T upstream_gene_variant PACA-CA X 153188805 153188805 single base substitution C A intron_variant PACA-CA X 153188805 153188805 single base substitution C A upstream_gene_variant PACA-CA X 153189576 153189576 single base substitution G A intron_variant PACA-CA X 153189576 153189576 single base substitution G A upstream_gene_variant PACA-CA X 153190349 153190349 single base substitution G A intron_variant PACA-CA X 153190349 153190349 single base substitution G A upstream_gene_variant PACA-CA X 153194714 153194714 single base substitution T C intron_variant PACA-CA X 153194714 153194714 single base substitution T C upstream_gene_variant PACA-CA X 153194816 153194816 single base substitution A G intron_variant PACA-CA X 153194816 153194816 single base substitution A G upstream_gene_variant PACA-CA X 153195996 153195996 single base substitution C T intron_variant PACA-CA X 153195996 153195996 single base substitution C T upstream_gene_variant PACA-CA X 153196839 153196839 single base substitution C T intron_variant PACA-CA X 153196839 153196839 single base substitution C T upstream_gene_variant PACA-CA X 153196958 153196958 single base substitution C T intron_variant PACA-CA X 153196958 153196958 single base substitution C T upstream_gene_variant PACA-CA X 153197687 153197687 single base substitution A G intron_variant PACA-CA X 153197687 153197687 single base substitution A G upstream_gene_variant PACA-CA X 153197823 153197823 single base substitution C T exon_variant PACA-CA X 153197823 153197823 single base substitution C T upstream_gene_variant PACA-CA X 153201358 153201358 single base substitution G A upstream_gene_variant PAEN-AU X 153184055 153184055 single base substitution G A downstream_gene_variant PAEN-AU X 153184055 153184055 single base substitution G A intron_variant PAEN-AU X 153184055 153184055 single base substitution G A upstream_gene_variant PAEN-AU X 153184784 153184784 single base substitution C T downstream_gene_variant PAEN-AU X 153184784 153184784 single base substitution C T intron_variant PAEN-AU X 153191511 153191511 single base substitution G T intron_variant PAEN-AU X 153191511 153191511 single base substitution G T upstream_gene_variant PAEN-AU X 153191512 153191512 single base substitution C G intron_variant PAEN-AU X 153191512 153191512 single base substitution C G upstream_gene_variant PAEN-AU X 153199973 153199973 single base substitution G A intron_variant PAEN-AU X 153204452 153204452 single base substitution G A upstream_gene_variant PBCA-DE X 153176574 153176574 single base substitution C T downstream_gene_variant PBCA-DE X 153176574 153176574 single base substitution C T intron_variant PBCA-DE X 153176574 153176574 single base substitution C T upstream_gene_variant PBCA-DE X 153189342 153189342 single base substitution C T intron_variant PBCA-DE X 153189342 153189342 single base substitution C T upstream_gene_variant PBCA-DE X 153189743 153189743 single base substitution C T intron_variant PBCA-DE X 153189743 153189743 single base substitution C T upstream_gene_variant PBCA-DE X 153195593 153195593 single base substitution A T intron_variant PBCA-DE X 153195593 153195593 single base substitution A T upstream_gene_variant PBCA-DE X 153197562 153197562 single base substitution C G exon_variant PBCA-DE X 153197562 153197562 single base substitution C G upstream_gene_variant PRAD-CA X 153177696 153177696 single base substitution G A downstream_gene_variant PRAD-CA X 153177696 153177696 single base substitution G A intron_variant PRAD-CA X 153177696 153177696 single base substitution G A upstream_gene_variant PRAD-CA X 153179936 153179936 single base substitution A G downstream_gene_variant PRAD-CA X 153179936 153179936 single base substitution A G intron_variant PRAD-CA X 153179936 153179936 single base substitution A G upstream_gene_variant PRAD-CA X 153204249 153204249 single base substitution G T upstream_gene_variant PRAD-US X 153187219 153187219 single base substitution C A exon_variant PRAD-US X 153187219 153187219 single base substitution C A synonymous_variant L14L 42G>T PRAD-US X 153187219 153187219 single base substitution C A synonymous_variant L37L 111G>T PRAD-US X 153187219 153187219 single base substitution C A upstream_gene_variant READ-US X 153175837 153175837 single base substitution C T 3_prime_UTR_variant READ-US X 153175837 153175837 single base substitution C T downstream_gene_variant READ-US X 153175837 153175837 single base substitution C T exon_variant READ-US X 153175837 153175837 single base substitution C T intron_variant READ-US X 153175837 153175837 single base substitution C T synonymous_variant E136E 408G>A READ-US X 153175837 153175837 single base substitution C T synonymous_variant E470E 1410G>A READ-US X 153175837 153175837 single base substitution C T synonymous_variant E625E 1875G>A READ-US X 153175837 153175837 single base substitution C T synonymous_variant E627E 1881G>A READ-US X 153175837 153175837 single base substitution C T synonymous_variant E648E 1944G>A READ-US X 153175837 153175837 single base substitution C T synonymous_variant E688E 2064G>A READ-US X 153175837 153175837 single base substitution C T upstream_gene_variant READ-US X 153186923 153186923 single base substitution C T exon_variant READ-US X 153186923 153186923 single base substitution C T synonymous_variant T110T 330G>A READ-US X 153186923 153186923 single base substitution C T synonymous_variant T87T 261G>A READ-US X 153186923 153186923 single base substitution C T upstream_gene_variant RECA-EU X 153171993 153171993 single base substitution A G downstream_gene_variant RECA-EU X 153190022 153190022 single base substitution G A intron_variant RECA-EU X 153190022 153190022 single base substitution G A upstream_gene_variant RECA-EU X 153194517 153194517 single base substitution C T intron_variant RECA-EU X 153194517 153194517 single base substitution C T upstream_gene_variant RECA-EU X 153195393 153195393 single base substitution G A intron_variant RECA-EU X 153195393 153195393 single base substitution G A upstream_gene_variant SKCA-BR X 153169367 153169367 single base substitution T G downstream_gene_variant SKCA-BR X 153170671 153170671 single base substitution G A downstream_gene_variant SKCA-BR X 153173679 153173679 single base substitution C T downstream_gene_variant SKCA-BR X 153173679 153173679 single base substitution C T intron_variant SKCA-BR X 153176125 153176125 single base substitution A C downstream_gene_variant SKCA-BR X 153176125 153176125 single base substitution A C intron_variant SKCA-BR X 153176125 153176125 single base substitution A C upstream_gene_variant SKCA-BR X 153177369 153177369 insertion of <=200bp - AT downstream_gene_variant SKCA-BR X 153177369 153177369 insertion of <=200bp - AT intron_variant SKCA-BR X 153177369 153177369 insertion of <=200bp - AT upstream_gene_variant SKCA-BR X 153177371 153177371 single base substitution A T downstream_gene_variant SKCA-BR X 153177371 153177371 single base substitution A T intron_variant SKCA-BR X 153177371 153177371 single base substitution A T upstream_gene_variant SKCA-BR X 153177589 153177589 single base substitution C T downstream_gene_variant SKCA-BR X 153177589 153177589 single base substitution C T intron_variant SKCA-BR X 153177589 153177589 single base substitution C T upstream_gene_variant SKCA-BR X 153185215 153185215 single base substitution G A downstream_gene_variant SKCA-BR X 153185215 153185215 single base substitution G A intron_variant SKCA-BR X 153185246 153185246 insertion of <=200bp - AT downstream_gene_variant SKCA-BR X 153185246 153185246 insertion of <=200bp - AT intron_variant SKCA-BR X 153189311 153189311 single base substitution A C intron_variant SKCA-BR X 153189311 153189311 single base substitution A C upstream_gene_variant SKCA-BR X 153193546 153193546 single base substitution G A intron_variant SKCA-BR X 153193546 153193546 single base substitution G A upstream_gene_variant SKCA-BR X 153193633 153193633 single base substitution G A intron_variant SKCA-BR X 153193633 153193633 single base substitution G A upstream_gene_variant SKCA-BR X 153200587 153200587 single base substitution G A upstream_gene_variant SKCA-BR X 153200964 153200964 single base substitution G A upstream_gene_variant SKCA-BR X 153202462 153202462 single base substitution A G upstream_gene_variant SKCM-US X 153170623 153170623 single base substitution C T downstream_gene_variant SKCM-US X 153171107 153171107 single base substitution G A downstream_gene_variant SKCM-US X 153171269 153171269 single base substitution C T downstream_gene_variant SKCM-US X 153174589 153174589 single base substitution G A 3_prime_UTR_variant SKCM-US X 153174589 153174589 single base substitution G A downstream_gene_variant SKCM-US X 153174589 153174589 single base substitution G A exon_variant SKCM-US X 153174589 153174589 single base substitution G A missense_variant P670S 2008C>T SKCM-US X 153174589 153174589 single base substitution G A missense_variant P825S 2473C>T SKCM-US X 153174589 153174589 single base substitution G A missense_variant P827S 2479C>T SKCM-US X 153174589 153174589 single base substitution G A missense_variant P848S 2542C>T SKCM-US X 153174589 153174589 single base substitution G A missense_variant P888S 2662C>T SKCM-US X 153175712 153175712 single base substitution T G 3_prime_UTR_variant SKCM-US X 153175712 153175712 single base substitution T G downstream_gene_variant SKCM-US X 153175712 153175712 single base substitution T G exon_variant SKCM-US X 153175712 153175712 single base substitution T G intron_variant SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q178P 533A>C SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q512P 1535A>C SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q667P 2000A>C SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q669P 2006A>C SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q690P 2069A>C SKCM-US X 153175712 153175712 single base substitution T G missense_variant Q730P 2189A>C SKCM-US X 153175712 153175712 single base substitution T G upstream_gene_variant SKCM-US X 153184723 153184723 single base substitution G A 3_prime_UTR_variant SKCM-US X 153184723 153184723 single base substitution G A downstream_gene_variant SKCM-US X 153184723 153184723 single base substitution G A exon_variant SKCM-US X 153184723 153184723 single base substitution G A intron_variant SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F119F 357C>T SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F209F 627C>T SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F211F 633C>T SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F232F 696C>T SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F272F 816C>T SKCM-US X 153184723 153184723 single base substitution G A synonymous_variant F7F 21C>T SKCM-US X 153186111 153186111 single base substitution G A 3_prime_UTR_variant SKCM-US X 153186111 153186111 single base substitution G A downstream_gene_variant SKCM-US X 153186111 153186111 single base substitution G A exon_variant SKCM-US X 153186111 153186111 single base substitution G A intron_variant SKCM-US X 153186111 153186111 single base substitution G A missense_variant S194F 581C>T SKCM-US X 153186111 153186111 single base substitution G A missense_variant S196F 587C>T SKCM-US X 153186111 153186111 single base substitution G A missense_variant S217F 650C>T SKCM-US X 153186111 153186111 single base substitution G A missense_variant S64F 191C>T SKCM-US X 153186111 153186111 single base substitution G A upstream_gene_variant SKCM-US X 153186238 153186238 single base substitution G A exon_variant SKCM-US X 153186238 153186238 single base substitution G A intron_variant SKCM-US X 153186238 153186238 single base substitution G A missense_variant H152Y 454C>T SKCM-US X 153186238 153186238 single base substitution G A missense_variant H154Y 460C>T SKCM-US X 153186238 153186238 single base substitution G A missense_variant H175Y 523C>T SKCM-US X 153186238 153186238 single base substitution G A missense_variant H22Y 64C>T SKCM-US X 153186238 153186238 single base substitution G A upstream_gene_variant SKCM-US X 153186550 153186550 single base substitution C T intron_variant SKCM-US X 153186550 153186550 single base substitution C T splice_region_variant SKCM-US X 153186550 153186550 single base substitution C T upstream_gene_variant SKCM-US X 153191630 153191630 single base substitution C T exon_variant SKCM-US X 153191630 153191630 single base substitution C T intron_variant SKCM-US X 153191630 153191630 single base substitution C T synonymous_variant R9R 27G>A SKCM-US X 153191630 153191630 single base substitution C T upstream_gene_variant SKCM-US X 153197787 153197787 single base substitution G A exon_variant SKCM-US X 153197787 153197787 single base substitution G A upstream_gene_variant STAD-US X 153171113 153171113 single base substitution G T downstream_gene_variant STAD-US X 153171222 153171222 single base substitution G A downstream_gene_variant STAD-US X 153171693 153171693 deletion of <=200bp G - downstream_gene_variant STAD-US X 153171758 153171758 single base substitution G T downstream_gene_variant STAD-US X 153171867 153171882 deletion of <=200bp GAAGGTGGGTGTAGCC - downstream_gene_variant STAD-US X 153171979 153171979 single base substitution G A downstream_gene_variant STAD-US X 153171980 153171980 single base substitution C T downstream_gene_variant STAD-US X 153171981 153171981 single base substitution G A downstream_gene_variant STAD-US X 153172147 153172147 single base substitution G A downstream_gene_variant STAD-US X 153173237 153173237 single base substitution G T 3_prime_UTR_variant STAD-US X 153173237 153173237 single base substitution G T downstream_gene_variant STAD-US X 153173237 153173237 single base substitution G T exon_variant STAD-US X 153173237 153173237 single base substitution G T synonymous_variant A751A 2253C>A STAD-US X 153173237 153173237 single base substitution G T synonymous_variant A906A 2718C>A STAD-US X 153173237 153173237 single base substitution G T synonymous_variant A908A 2724C>A STAD-US X 153173237 153173237 single base substitution G T synonymous_variant A929A 2787C>A STAD-US X 153173237 153173237 single base substitution G T synonymous_variant A969A 2907C>A STAD-US X 153174968 153174968 single base substitution G A 3_prime_UTR_variant STAD-US X 153174968 153174968 single base substitution G A downstream_gene_variant STAD-US X 153174968 153174968 single base substitution G A exon_variant STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G233G 699C>T STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G634G 1902C>T STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G789G 2367C>T STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G791G 2373C>T STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G812G 2436C>T STAD-US X 153174968 153174968 single base substitution G A synonymous_variant G852G 2556C>T STAD-US X 153175255 153175255 single base substitution C T 3_prime_UTR_variant STAD-US X 153175255 153175255 single base substitution C T downstream_gene_variant STAD-US X 153175255 153175255 single base substitution C T exon_variant STAD-US X 153175255 153175255 single base substitution C T missense_variant R206Q 617G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R273Q 818G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R607Q 1820G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R762Q 2285G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R764Q 2291G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R785Q 2354G>A STAD-US X 153175255 153175255 single base substitution C T missense_variant R825Q 2474G>A STAD-US X 153175255 153175255 single base substitution C T upstream_gene_variant STAD-US X 153175711 153175711 single base substitution C T 3_prime_UTR_variant STAD-US X 153175711 153175711 single base substitution C T downstream_gene_variant STAD-US X 153175711 153175711 single base substitution C T exon_variant STAD-US X 153175711 153175711 single base substitution C T intron_variant STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q178Q 534G>A STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q512Q 1536G>A STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q667Q 2001G>A STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q669Q 2007G>A STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q690Q 2070G>A STAD-US X 153175711 153175711 single base substitution C T synonymous_variant Q730Q 2190G>A STAD-US X 153175711 153175711 single base substitution C T upstream_gene_variant STAD-US X 153175819 153175819 single base substitution G A 3_prime_UTR_variant STAD-US X 153175819 153175819 single base substitution G A downstream_gene_variant STAD-US X 153175819 153175819 single base substitution G A exon_variant STAD-US X 153175819 153175819 single base substitution G A intron_variant STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y142Y 426C>T STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y476Y 1428C>T STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y631Y 1893C>T STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y633Y 1899C>T STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y654Y 1962C>T STAD-US X 153175819 153175819 single base substitution G A synonymous_variant Y694Y 2082C>T STAD-US X 153175819 153175819 single base substitution G A upstream_gene_variant STAD-US X 153176006 153176006 single base substitution C T 3_prime_UTR_variant STAD-US X 153176006 153176006 single base substitution C T downstream_gene_variant STAD-US X 153176006 153176006 single base substitution C T exon_variant STAD-US X 153176006 153176006 single base substitution C T intron_variant STAD-US X 153176006 153176006 single base substitution C T missense_variant A114T 340G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A125T 373G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A448T 1342G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A603T 1807G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A605T 1813G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A626T 1876G>A STAD-US X 153176006 153176006 single base substitution C T missense_variant A666T 1996G>A STAD-US X 153176006 153176006 single base substitution C T upstream_gene_variant STAD-US X 153178181 153178182 deletion of <=200bp AA - 3_prime_UTR_variant STAD-US X 153178181 153178182 deletion of <=200bp AA - downstream_gene_variant STAD-US X 153178181 153178182 deletion of <=200bp AA - exon_variant STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F19 STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F327 STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F482 STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F484 STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F505 STAD-US X 153178181 153178182 deletion of <=200bp AA - frameshift_variant F545 STAD-US X 153178181 153178182 deletion of <=200bp AA - upstream_gene_variant STAD-US X 153184481 153184481 single base substitution G T 3_prime_UTR_variant STAD-US X 153184481 153184481 single base substitution G T downstream_gene_variant STAD-US X 153184481 153184481 single base substitution G T exon_variant STAD-US X 153184481 153184481 single base substitution G T intron_variant STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A166A 498C>A STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A256A 768C>A STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A258A 774C>A STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A279A 837C>A STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A319A 957C>A STAD-US X 153184481 153184481 single base substitution G T synonymous_variant A54A 162C>A STAD-US X 153184481 153184481 single base substitution G T upstream_gene_variant STAD-US X 153184643 153184643 single base substitution T C 3_prime_UTR_variant STAD-US X 153184643 153184643 single base substitution T C downstream_gene_variant STAD-US X 153184643 153184643 single base substitution T C exon_variant STAD-US X 153184643 153184643 single base substitution T C intron_variant STAD-US X 153184643 153184643 single base substitution T C missense_variant N146S 437A>G STAD-US X 153184643 153184643 single base substitution T C missense_variant N236S 707A>G STAD-US X 153184643 153184643 single base substitution T C missense_variant N238S 713A>G STAD-US X 153184643 153184643 single base substitution T C missense_variant N259S 776A>G STAD-US X 153184643 153184643 single base substitution T C missense_variant N299S 896A>G STAD-US X 153184643 153184643 single base substitution T C missense_variant N34S 101A>G STAD-US X 153184643 153184643 single base substitution T C upstream_gene_variant STAD-US X 153191699 153191699 single base substitution C T 5_prime_UTR_variant STAD-US X 153191699 153191699 single base substitution C T intron_variant STAD-US X 153191699 153191699 single base substitution C T upstream_gene_variant THCA-SA X 153175295 153175295 single base substitution C A 3_prime_UTR_variant THCA-SA X 153175295 153175295 single base substitution C A downstream_gene_variant THCA-SA X 153175295 153175295 single base substitution C A exon_variant THCA-SA X 153175295 153175295 single base substitution C A missense_variant V193L 577G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V260L 778G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V594L 1780G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V749L 2245G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V751L 2251G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V772L 2314G>T THCA-SA X 153175295 153175295 single base substitution C A missense_variant V812L 2434G>T THCA-SA X 153175295 153175295 single base substitution C A upstream_gene_variant THCA-SA X 153175722 153175722 single base substitution G T 3_prime_UTR_variant THCA-SA X 153175722 153175722 single base substitution G T downstream_gene_variant THCA-SA X 153175722 153175722 single base substitution G T exon_variant THCA-SA X 153175722 153175722 single base substitution G T intron_variant THCA-SA X 153175722 153175722 single base substitution G T missense_variant L175I 523C>A THCA-SA X 153175722 153175722 single base substitution G T missense_variant L509I 1525C>A THCA-SA X 153175722 153175722 single base substitution G T missense_variant L664I 1990C>A THCA-SA X 153175722 153175722 single base substitution G T missense_variant L666I 1996C>A THCA-SA X 153175722 153175722 single base substitution G T missense_variant L687I 2059C>A THCA-SA X 153175722 153175722 single base substitution G T missense_variant L727I 2179C>A THCA-SA X 153175722 153175722 single base substitution G T upstream_gene_variant THCA-SA X 153184483 153184483 single base substitution C T 3_prime_UTR_variant THCA-SA X 153184483 153184483 single base substitution C T downstream_gene_variant THCA-SA X 153184483 153184483 single base substitution C T exon_variant THCA-SA X 153184483 153184483 single base substitution C T intron_variant THCA-SA X 153184483 153184483 single base substitution C T missense_variant A166T 496G>A THCA-SA X 153184483 153184483 single base substitution C T missense_variant A256T 766G>A THCA-SA X 153184483 153184483 single base substitution C T missense_variant A258T 772G>A THCA-SA X 153184483 153184483 single base substitution C T missense_variant A279T 835G>A THCA-SA X 153184483 153184483 single base substitution C T missense_variant A319T 955G>A THCA-SA X 153184483 153184483 single base substitution C T missense_variant A54T 160G>A THCA-SA X 153184483 153184483 single base substitution C T upstream_gene_variant THCA-SA X 153195393 153195393 single base substitution G A intron_variant THCA-SA X 153195393 153195393 single base substitution G A upstream_gene_variant THCA-US X 153184648 153184648 single base substitution G A 3_prime_UTR_variant THCA-US X 153184648 153184648 single base substitution G A downstream_gene_variant THCA-US X 153184648 153184648 single base substitution G A exon_variant THCA-US X 153184648 153184648 single base substitution G A intron_variant THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V144V 432C>T THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V234V 702C>T THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V236V 708C>T THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V257V 771C>T THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V297V 891C>T THCA-US X 153184648 153184648 single base substitution G A synonymous_variant V32V 96C>T THCA-US X 153184648 153184648 single base substitution G A upstream_gene_variant THCA-US X 153186831 153186831 single base substitution C G exon_variant THCA-US X 153186831 153186831 single base substitution C G missense_variant R118P 353G>C THCA-US X 153186831 153186831 single base substitution C G missense_variant R141P 422G>C THCA-US X 153186831 153186831 single base substitution C G missense_variant R9P 26G>C THCA-US X 153186831 153186831 single base substitution C G upstream_gene_variant UCEC-US X 153171047 153171047 single base substitution G T downstream_gene_variant UCEC-US X 153171162 153171162 single base substitution C T downstream_gene_variant UCEC-US X 153171297 153171297 single base substitution C T downstream_gene_variant UCEC-US X 153171375 153171375 single base substitution C T downstream_gene_variant UCEC-US X 153171406 153171406 single base substitution G A downstream_gene_variant UCEC-US X 153171578 153171578 single base substitution C T downstream_gene_variant UCEC-US X 153171602 153171602 single base substitution C T downstream_gene_variant UCEC-US X 153174577 153174577 single base substitution T G 3_prime_UTR_variant UCEC-US X 153174577 153174577 single base substitution T G downstream_gene_variant UCEC-US X 153174577 153174577 single base substitution T G exon_variant UCEC-US X 153174577 153174577 single base substitution T G synonymous_variant R674R 2020A>C UCEC-US X 153174577 153174577 single base substitution T G synonymous_variant R829R 2485A>C UCEC-US X 153174577 153174577 single base substitution T G synonymous_variant R831R 2491A>C UCEC-US X 153174577 153174577 single base substitution T G synonymous_variant R852R 2554A>C UCEC-US X 153174577 153174577 single base substitution T G synonymous_variant R892R 2674A>C UCEC-US X 153174592 153174592 single base substitution C T 3_prime_UTR_variant UCEC-US X 153174592 153174592 single base substitution C T downstream_gene_variant UCEC-US X 153174592 153174592 single base substitution C T exon_variant UCEC-US X 153174592 153174592 single base substitution C T missense_variant G669R 2005G>A UCEC-US X 153174592 153174592 single base substitution C T missense_variant G824R 2470G>A UCEC-US X 153174592 153174592 single base substitution C T missense_variant G826R 2476G>A UCEC-US X 153174592 153174592 single base substitution C T missense_variant G847R 2539G>A UCEC-US X 153174592 153174592 single base substitution C T missense_variant G887R 2659G>A UCEC-US X 153174959 153174959 single base substitution C T 3_prime_UTR_variant UCEC-US X 153174959 153174959 single base substitution C T downstream_gene_variant UCEC-US X 153174959 153174959 single base substitution C T exon_variant UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L236L 708G>A UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L637L 1911G>A UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L792L 2376G>A UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L794L 2382G>A UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L815L 2445G>A UCEC-US X 153174959 153174959 single base substitution C T synonymous_variant L855L 2565G>A UCEC-US X 153175478 153175478 single base substitution C T 3_prime_UTR_variant UCEC-US X 153175478 153175478 single base substitution C T downstream_gene_variant UCEC-US X 153175478 153175478 single base substitution C T exon_variant UCEC-US X 153175478 153175478 single base substitution C T missense_variant A161T 481G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A228T 682G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A562T 1684G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A717T 2149G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A719T 2155G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A740T 2218G>A UCEC-US X 153175478 153175478 single base substitution C T missense_variant A780T 2338G>A UCEC-US X 153175478 153175478 single base substitution C T upstream_gene_variant UCEC-US X 153175682 153175682 single base substitution G A 3_prime_UTR_variant UCEC-US X 153175682 153175682 single base substitution G A downstream_gene_variant UCEC-US X 153175682 153175682 single base substitution G A exon_variant UCEC-US X 153175682 153175682 single base substitution G A intron_variant UCEC-US X 153175682 153175682 single base substitution G A missense_variant S188L 563C>T UCEC-US X 153175682 153175682 single base substitution G A missense_variant S522L 1565C>T UCEC-US X 153175682 153175682 single base substitution G A missense_variant S677L 2030C>T UCEC-US X 153175682 153175682 single base substitution G A missense_variant S679L 2036C>T UCEC-US X 153175682 153175682 single base substitution G A missense_variant S700L 2099C>T UCEC-US X 153175682 153175682 single base substitution G A missense_variant S740L 2219C>T UCEC-US X 153175682 153175682 single base substitution G A upstream_gene_variant UCEC-US X 153176393 153176393 single base substitution C T 3_prime_UTR_variant UCEC-US X 153176393 153176393 single base substitution C T downstream_gene_variant UCEC-US X 153176393 153176393 single base substitution C T exon_variant UCEC-US X 153176393 153176393 single base substitution C T intron_variant UCEC-US X 153176393 153176393 single base substitution C T missense_variant R377H 1130G>A UCEC-US X 153176393 153176393 single base substitution C T missense_variant R532H 1595G>A UCEC-US X 153176393 153176393 single base substitution C T missense_variant R534H 1601G>A UCEC-US X 153176393 153176393 single base substitution C T missense_variant R54H 161G>A UCEC-US X 153176393 153176393 single base substitution C T missense_variant R555H 1664G>A UCEC-US X 153176393 153176393 single base substitution C T missense_variant R595H 1784G>A UCEC-US X 153176393 153176393 single base substitution C T upstream_gene_variant UCEC-US X 153176611 153176611 single base substitution C T 3_prime_UTR_variant UCEC-US X 153176611 153176611 single base substitution C T downstream_gene_variant UCEC-US X 153176611 153176611 single base substitution C T exon_variant UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E347E 1041G>A UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E39E 117G>A UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E502E 1506G>A UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E504E 1512G>A UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E525E 1575G>A UCEC-US X 153176611 153176611 single base substitution C T synonymous_variant E565E 1695G>A UCEC-US X 153176611 153176611 single base substitution C T upstream_gene_variant UCEC-US X 153178166 153178166 single base substitution C A 3_prime_UTR_variant UCEC-US X 153178166 153178166 single base substitution C A downstream_gene_variant UCEC-US X 153178166 153178166 single base substitution C A exon_variant UCEC-US X 153178166 153178166 single base substitution C A missense_variant E24D 72G>T UCEC-US X 153178166 153178166 single base substitution C A missense_variant E332D 996G>T UCEC-US X 153178166 153178166 single base substitution C A missense_variant E487D 1461G>T UCEC-US X 153178166 153178166 single base substitution C A missense_variant E489D 1467G>T UCEC-US X 153178166 153178166 single base substitution C A missense_variant E510D 1530G>T UCEC-US X 153178166 153178166 single base substitution C A missense_variant E550D 1650G>T UCEC-US X 153178166 153178166 single base substitution C A upstream_gene_variant UCEC-US X 153178235 153178235 single base substitution T A 3_prime_UTR_variant UCEC-US X 153178235 153178235 single base substitution T A downstream_gene_variant UCEC-US X 153178235 153178235 single base substitution T A exon_variant UCEC-US X 153178235 153178235 single base substitution T A missense_variant K1N 3A>T UCEC-US X 153178235 153178235 single base substitution T A missense_variant K309N 927A>T UCEC-US X 153178235 153178235 single base substitution T A missense_variant K464N 1392A>T UCEC-US X 153178235 153178235 single base substitution T A missense_variant K466N 1398A>T UCEC-US X 153178235 153178235 single base substitution T A missense_variant K487N 1461A>T UCEC-US X 153178235 153178235 single base substitution T A missense_variant K527N 1581A>T UCEC-US X 153178235 153178235 single base substitution T A upstream_gene_variant UCEC-US X 153184317 153184317 single base substitution C T 3_prime_UTR_variant UCEC-US X 153184317 153184317 single base substitution C T downstream_gene_variant UCEC-US X 153184317 153184317 single base substitution C T exon_variant UCEC-US X 153184317 153184317 single base substitution C T intron_variant UCEC-US X 153184317 153184317 single base substitution C T missense_variant R109H 326G>A UCEC-US X 153184317 153184317 single base substitution C T missense_variant R311H 932G>A UCEC-US X 153184317 153184317 single base substitution C T missense_variant R313H 938G>A UCEC-US X 153184317 153184317 single base substitution C T missense_variant R334H 1001G>A UCEC-US X 153184317 153184317 single base substitution C T missense_variant R374H 1121G>A UCEC-US X 153184317 153184317 single base substitution C T upstream_gene_variant UCEC-US X 153184500 153184500 single base substitution T G 3_prime_UTR_variant UCEC-US X 153184500 153184500 single base substitution T G downstream_gene_variant UCEC-US X 153184500 153184500 single base substitution T G exon_variant UCEC-US X 153184500 153184500 single base substitution T G intron_variant UCEC-US X 153184500 153184500 single base substitution T G missense_variant D160A 479A>C UCEC-US X 153184500 153184500 single base substitution T G missense_variant D250A 749A>C UCEC-US X 153184500 153184500 single base substitution T G missense_variant D252A 755A>C UCEC-US X 153184500 153184500 single base substitution T G missense_variant D273A 818A>C UCEC-US X 153184500 153184500 single base substitution T G missense_variant D313A 938A>C UCEC-US X 153184500 153184500 single base substitution T G missense_variant D48A 143A>C UCEC-US X 153184500 153184500 single base substitution T G upstream_gene_variant UCEC-US X 153184624 153184624 single base substitution G T 3_prime_UTR_variant UCEC-US X 153184624 153184624 single base substitution G T downstream_gene_variant UCEC-US X 153184624 153184624 single base substitution G T exon_variant UCEC-US X 153184624 153184624 single base substitution G T intron_variant UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V152V 456C>A UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V242V 726C>A UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V244V 732C>A UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V265V 795C>A UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V305V 915C>A UCEC-US X 153184624 153184624 single base substitution G T synonymous_variant V40V 120C>A UCEC-US X 153184624 153184624 single base substitution G T upstream_gene_variant UCEC-US X 153185024 153185024 single base substitution A G downstream_gene_variant UCEC-US X 153185024 153185024 single base substitution A G intron_variant UCEC-US X 153185024 153185024 single base substitution A G synonymous_variant H113H 339T>C UCEC-US X 153185024 153185024 single base substitution A G synonymous_variant H266H 798T>C UCEC-US X 153185124 153185124 single base substitution C T downstream_gene_variant UCEC-US X 153185124 153185124 single base substitution C T intron_variant UCEC-US X 153185124 153185124 single base substitution C T missense_variant R233K 698G>A UCEC-US X 153185124 153185124 single base substitution C T missense_variant R80K 239G>A UCEC-US X 153186165 153186165 single base substitution C A downstream_gene_variant UCEC-US X 153186165 153186165 single base substitution C A exon_variant UCEC-US X 153186165 153186165 single base substitution C A intron_variant UCEC-US X 153186165 153186165 single base substitution C A missense_variant S176I 527G>T UCEC-US X 153186165 153186165 single base substitution C A missense_variant S178I 533G>T UCEC-US X 153186165 153186165 single base substitution C A missense_variant S199I 596G>T UCEC-US X 153186165 153186165 single base substitution C A missense_variant S46I 137G>T UCEC-US X 153186165 153186165 single base substitution C A upstream_gene_variant UCEC-US X 153187214 153187214 single base substitution C T exon_variant UCEC-US X 153187214 153187214 single base substitution C T missense_variant G16D 47G>A UCEC-US X 153187214 153187214 single base substitution C T missense_variant G39D 116G>A UCEC-US X 153187214 153187214 single base substitution C T upstream_gene_variant UCEC-US X 153195637 153195637 single base substitution C T intron_variant UCEC-US X 153195637 153195637 single base substitution C T upstream_gene_variant UCEC-US X 153199858 153199858 single base substitution T C exon_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-A6-6781-01 COSM1466669 c.271C>T p.R91W Substitution - Missense 23:153921606-153921606 - MO_1008 COSM377326 c.733G>A p.E245K Substitution - Missense 23:153919232-153919232 - CHC892T COSM4793676 c.393C>T p.R131R Substitution - coding silent 23:153921407-153921407 - TCGA-AX-A0J1-01 COSM1117646 c.2539G>A p.G847R Substitution - Missense 23:153909138-153909138 - LUAD-F00368 COSM367839 c.354G>T p.A118A Substitution - coding silent 23:153921446-153921446 - TCGA-AY-6197-01 COSM1466671 c.242T>C p.L81P Substitution - Missense 23:153921635-153921635 - TCGA-B5-A0JY-01 COSM1117644 c.2554A>C p.R852R Substitution - coding silent 23:153909123-153909123 - C086 COSM3913639 c.696C>T p.F232F Substitution - coding silent 23:153919269-153919269 - TARGET-20-PAKIYW-09A-01D COSM5487157 c.272G>A p.R91Q Substitution - Missense 23:153921605-153921605 - BN34T COSM3708516 c.1324A>G p.T442A Substitution - Missense 23:153913411-153913411 - LS174T COSM3236371 c.641G>A p.R214H Substitution - Missense 23:153920666-153920666 - TCGA-EK-A2R8-01 COSM4822597 c.1575G>C p.E525D Substitution - Missense 23:153911157-153911157 - MD-279 COSM301695 c.267C>T p.S89S Substitution - coding silent 23:153921610-153921610 - TCGA-EK-A3GK-01 COSM4853255 c.574G>T p.E192* Substitution - Nonsense 23:153920733-153920733 - TCGA-D3-A51T-06 COSM3559601 c.650C>T p.S217F Substitution - Missense 23:153920657-153920657 - TCGA-36-2545-01 COSM1331147 c.2682A>G p.P894P Substitution - coding silent 23:153907888-153907888 - ATL078 COSM4171921 c.1_8delATGGCCGC p.? Unknown LS174T COSM4646243 c.217C>T p.R73C Substitution - Missense 23:153921660-153921660 - sysucc-1370T COSM5472847 c.2560C>T p.R854C Substitution - Missense 23:153909117-153909117 - S01861 COSM5671493 c.2278C>T p.R760C Substitution - Missense 23:153909877-153909877 - CSCC-17-T COSM4469514 c.1482C>T p.P494P Substitution - coding silent 23:153912760-153912760 - 585205 COSM318759 c.508A>G p.T170A Substitution - Missense 23:153920799-153920799 - TCGA-EE-A3J5-06 COSM3559599 c.2069A>C p.Q690P Substitution - Missense 23:153910258-153910258 - TCGA-BR-4362-01 COSM4107943 c.776A>G p.N259S Substitution - Missense 23:153919189-153919189 - TCGA-B5-A0K9-01 COSM1117648 c.2445G>A p.L815L Substitution - coding silent 23:153909505-153909505 - CSCC-35-T COSM4536212 c.2158G>A p.D720N Substitution - Missense 23:153910084-153910084 - 405 COSM4430116 c.1827C>T p.A609A Substitution - coding silent 23:153910601-153910601 - Pat_41_B COSM5877393 c.448G>A p.E150K Substitution - Missense 23:153921147-153921147 - TCGA-F5-6814-01 COSM3424618 c.1944G>A p.E648E Substitution - coding silent 23:153910383-153910383 - TCGA-DM-A1DA-01 COSM1466656 c.2231A>G p.D744G Substitution - Missense 23:153909924-153909924 - HCT-15 COSM1683023 c.2279G>A p.R760H Substitution - Missense 23:153909876-153909876 - Gp2D COSM3236365 c.801C>T p.D267D Substitution - coding silent 23:153919164-153919164 - PD11750a COSM5786549 c.2714G>A p.R905Q Substitution - Missense 23:153907856-153907856 - TCGA-AA-A01D-01 COSM5121441 c.792C>T p.D264D Substitution - coding silent 23:153919173-153919173 - TCGA-B5-A11J-01 COSM1117654 c.1664G>A p.R555H Substitution - Missense 23:153910939-153910939 - T3431 COSM4662932 c.1103G>A p.R368H Substitution - Missense 23:153913809-153913809 - TCGA-CL-4957-01 COSM3424620 c.330G>A p.T110T Substitution - coding silent 23:153921470-153921470 - TCGA-AN-A0FX-01 COSM5835901 c.2774_2775insC p.G926fs*>22 Insertion - Frameshift 23:153907795-153907796 - Au5 COSM5605548 c.1359C>T p.I453I Substitution - coding silent 23:153913270-153913270 - SJBALL021083_D1 COSM4994022 c.615T>C p.A205A Substitution - coding silent 23:153920692-153920692 - SE30PT COSM1580271 c.2732C>A p.P911H Substitution - Missense 23:153907838-153907838 - TCGA-76-6661-01 COSM3406128 c.1972G>A p.V658M Substitution - Missense 23:153910355-153910355 - TCGA-CM-6674-01 COSM1466660 c.1474C>T p.R492C Substitution - Missense 23:153912768-153912768 - TCGA-13-2057-01 COSM1331145 c.2241G>C p.G747G Substitution - coding silent 23:153909914-153909914 - 587316 COSM1183450 c.626A>C p.E209A Substitution - Missense 23:153920681-153920681 - TCGA-CD-8536-01 COSM4107929 c.2787C>A p.A929A Substitution - coding silent 23:153907783-153907783 - TCGA-BR-6852-01 COSM4107931 c.2436C>T p.G812G Substitution - coding silent 23:153909514-153909514 - TCGA-A5-A0VP-01 COSM1117650 c.2218G>A p.A740T Substitution - Missense 23:153910024-153910024 - TCGA-AB-2898-03 COSM1319476 c.375C>T p.A125A Substitution - coding silent 23:153921425-153921425 - Gp5D COSM3236365 c.801C>T p.D267D Substitution - coding silent 23:153919164-153919164 - sysucc-783T COSM5485144 c.1048G>A p.V350I Substitution - Missense 23:153913864-153913864 - CHC1731T COSM4792087 c.1356C>T p.S452S Substitution - coding silent 23:153913273-153913273 - SA2 COSM1166357 c.1354A>G p.S452G Substitution - Missense 23:153913275-153913275 - TCGA-IR-A3LK-01 COSM4816932 c.523C>G p.H175D Substitution - Missense 23:153920784-153920784 - AOCS-152-1-X COSM4137764 c.498+1G>C p.? Unknown 23:153921096-153921096 - RK308_C01 COSM3747380 c.79C>T p.Q27* Substitution - Nonsense 23:153921798-153921798 - 2492702 COSM5599084 c.471C>T p.L157L Substitution - coding silent 23:153921124-153921124 - T3021 COSM4662924 c.2363A>G p.H788R Substitution - Missense 23:153909792-153909792 - TCGA-D1-A103-01 COSM1117671 c.596G>T p.S199I Substitution - Missense 23:153920711-153920711 - TCGA-EB-A5UN-06 COSM3559607 c.27G>A p.R9R Substitution - coding silent 23:153926176-153926176 - TCGA-FS-A1ZZ-06 COSM3559605 c.498G>A p.T166T Substitution - coding silent 23:153921097-153921097 - TCGA-A7-A26J-01 COSM5835903 c.2476delG p.E826fs*114 Deletion - Frameshift 23:153909474-153909474 - HT29 COSM3236357 c.1068C>G p.D356E Substitution - Missense 23:153913844-153913844 - HCT15 COSM1683023 c.2279G>A p.R760H Substitution - Missense 23:153909876-153909876 - HT29 COSM3236325 c.2263T>G p.F755V Substitution - Missense 23:153909892-153909892 - CHC892T COSM4793676 c.393C>T p.R131R Substitution - coding silent 23:153921407-153921407 - T3670 COSM4662938 c.238C>T p.R80C Substitution - Missense 23:153921639-153921639 - TCGA-B5-A0JY-01 COSM1117668 c.795C>A p.V265V Substitution - coding silent 23:153919170-153919170 - HCC2998 COSM1683025 c.721A>G p.K241E Substitution - Missense 23:153919244-153919244 - TCGA-BS-A0UV-01 COSM1117656 c.1575G>A p.E525E Substitution - coding silent 23:153911157-153911157 - DLD1 COSM1683023 c.2279G>A p.R760H Substitution - Missense 23:153909876-153909876 - BN34 COSM3708516 c.1324A>G p.T442A Substitution - Missense 23:153913411-153913411 - TCGA-CM-4744-01 COSM1466658 c.2118C>T p.Y706Y Substitution - coding silent 23:153910209-153910209 - TCGA-AP-A0LM-01 COSM1117652 c.2099C>T p.S700L Substitution - Missense 23:153910228-153910228 - T2991 COSM4662922 c.2755A>T p.K919* Substitution - Nonsense 23:153907815-153907815 - 5_tFL COSM4171921 c.1_8delATGGCCGC p.? Unknown PTC-54C COSM4156725 c.311C>T p.A104V Substitution - Missense 23:153921489-153921489 - T207 COSM4662928 c.2057C>T p.T686M Substitution - Missense 23:153910270-153910270 - TCGA-AA-A010-01 COSM278957 c.1508G>T p.R503I Substitution - Missense 23:153912734-153912734 - 2492703 COSM5599084 c.471C>T p.L157L Substitution - coding silent 23:153921124-153921124 - CHEWS008 COSM4589289 c.2004C>T p.P668P Substitution - coding silent 23:153910323-153910323 - TCGA-A5-A0G5-01 COSM1117662 c.1461A>T p.K487N Substitution - Missense 23:153912781-153912781 - 2290929 COSM4440657 c.1486C>T p.P496S Substitution - Missense 23:153912756-153912756 - TCGA-LP-A4AV-01 COSM4825113 c.1530G>C p.E510D Substitution - Missense 23:153912712-153912712 - TCGA-AY-6386-01 COSM1466654 c.2320C>T p.R774W Substitution - Missense 23:153909835-153909835 - PCSI_0083_Pa_P COSM3379572 c.1542+1G>A p.? Unknown 23:153912699-153912699 - Gp2D COSM4628999 c.2042A>G p.N681S Substitution - Missense 23:153910285-153910285 - S02139 COSM5674709 c.2591A>C p.H864P Substitution - Missense 23:153909086-153909086 - ESCC_47 COSM1466662 c.1194C>T p.D398D Substitution - coding silent 23:153913541-153913541 - ccRCC-38 COSM1660611 c.2752A>C p.N918H Substitution - Missense 23:153907818-153907818 - Au2 COSM5599084 c.471C>T p.L157L Substitution - coding silent 23:153921124-153921124 - LUAD-QCHM7 COSM377326 c.733G>A p.E245K Substitution - Missense 23:153919232-153919232 - TCGA-A5-A0GP-01 COSM1117666 c.818A>C p.D273A Substitution - Missense 23:153919046-153919046 - TCGA-C5-A7CL-01 COSM4837855 c.1681+1G>C p.? Unknown 23:153910921-153910921 - 18472 COSM5616263 c.421C>T p.R141C Substitution - Missense 23:153921379-153921379 - CX-1 COSM3236325 c.2263T>G p.F755V Substitution - Missense 23:153909892-153909892 - BCM423T COSM4802603 c.595A>T p.S199C Substitution - Missense 23:153920712-153920712 - PTC-70C COSM4156723 c.1716T>C p.H572H Substitution - coding silent 23:153910800-153910800 - 5_FL COSM4171921 c.1_8delATGGCCGC p.? Unknown S02384 COSM5698653 c.2293C>A p.L765M Substitution - Missense 23:153909862-153909862 - TCGA-C8-A26X-01 COSM1490663 c.2430G>T p.V810V Substitution - coding silent 23:153909520-153909520 - C135 COSM4618910 c.2126G>A p.C709Y Substitution - Missense 23:153910201-153910201 - S00356 COSM309245 c.2465G>T p.G822V Substitution - Missense 23:153909485-153909485 - HCC021T COSM5815735 c.2173A>T p.S725C Substitution - Missense 23:153910069-153910069 - TCGA-BR-4363-01 COSM4107935 c.2070G>A p.Q690Q Substitution - coding silent 23:153910257-153910257 - 2328683 COSM1117650 c.2218G>A p.A740T Substitution - Missense 23:153910024-153910024 - HCC2998 COSM1683025 c.721A>G p.K241E Substitution - Missense 23:153919244-153919244 - TCGA-EB-A3XD-01 COSM3559603 c.523C>T p.H175Y Substitution - Missense 23:153920784-153920784 - 2492700 COSM5599084 c.471C>T p.L157L Substitution - coding silent 23:153921124-153921124 - pfg228T COSM4762855 c.865G>A p.A289T Substitution - Missense 23:153918999-153918999 - TCGA-HC-7752-01 COSM3673360 c.111G>T p.L37L Substitution - coding silent 23:153921766-153921766 - LS180 COSM4646243 c.217C>T p.R73C Substitution - Missense 23:153921660-153921660 - HN_62756 COSM127355 c.510G>A p.T170T Substitution - coding silent 23:153920797-153920797 - PTC_218 COSM5959906 c.835G>A p.A279T Substitution - Missense 23:153919029-153919029 - HCT8 COSM1683023 c.2279G>A p.R760H Substitution - Missense 23:153909876-153909876 - CCK81 COSM4620884 c.2135C>A p.P712Q Substitution - Missense 23:153910192-153910192 - TCGA-14-0813-01 COSM1117664 c.1001G>A p.R334H Substitution - Missense 23:153918863-153918863 - TCGA-HJ-7597-01 COSM4107933 c.2354G>A p.R785Q Substitution - Missense 23:153909801-153909801 - I2L-P7-Tumor-Organoid COSM5367399 c.2328C>T p.H776H Substitution - coding silent 23:153909827-153909827 - BD110T COSM1466658 c.2118C>T p.Y706Y Substitution - coding silent 23:153910209-153910209 - ATL035 COSM5711547 c.1964A>G p.N655S Substitution - Missense 23:153910363-153910363 - 2290930 COSM4440657 c.1486C>T p.P496S Substitution - Missense 23:153912756-153912756 - 2250220 COSM5030455 c.1412-9A>G p.? Unknown 23:153913060-153913060 - HT55 COSM3236383 c.326A>T p.H109L Substitution - Missense 23:153921474-153921474 - TCGA-DH-5144-01 COSM3973441 c.2160C>T p.D720D Substitution - coding silent 23:153910082-153910082 - CSCC-47-T COSM4510254 c.711C>G p.L237L Substitution - coding silent 23:153919254-153919254 - BCM423T COSM4802603 c.595A>T p.S199C Substitution - Missense 23:153920712-153920712 - TCGA-BS-A0UV-01 COSM1117664 c.1001G>A p.R334H Substitution - Missense 23:153918863-153918863 - ESCC_BICR_023T COSM5436555 c.1129G>C p.E377Q Substitution - Missense 23:153913783-153913783 - PTC-54C COSM4156723 c.1716T>C p.H572H Substitution - coding silent 23:153910800-153910800 - TCGA-CK-6746-01 COSM1466666 c.776A>T p.N259I Substitution - Missense 23:153919189-153919189 - SW480 COSM3236343 c.2063T>C p.I688T Substitution - Missense 23:153910264-153910264 - T228 COSM4662926 c.2184G>A p.A728A Substitution - coding silent 23:153910058-153910058 - T55 COSM4662936 c.331C>T p.R111W Substitution - Missense 23:153921469-153921469 - T3024 COSM4662934 c.1033-2A>G p.? Unknown 23:153913881-153913881 - TCGA-A6-5665-01 COSM5090370 c.168C>T p.R56R Substitution - coding silent 23:153921709-153921709 - 08-P462 COSM3236319 c.2741G>A p.R914H Substitution - Missense 23:153907829-153907829 - TCGA-66-2773-01 COSM755727 c.2687C>G p.S896C Substitution - Missense 23:153907883-153907883 - sysucc-834T COSM5486786 c.164G>A p.R55H Substitution - Missense 23:153921713-153921713 - TCGA-DJ-A4UT-01 COSM3236367 c.771C>T p.V257V Substitution - coding silent 23:153919194-153919194 - LS180 COSM3236371 c.641G>A p.R214H Substitution - Missense 23:153920666-153920666 - TCGA-AA-3710-01 COSM5105822 c.281C>A p.P94Q Substitution - Missense 23:153921519-153921519 - 2024537 COSM1716519 c.2209G>T p.E737* Substitution - Nonsense 23:153910033-153910033 - T30 COSM5345949 c.282G>A p.P94P Substitution - coding silent 23:153921518-153921518 - TCGA-BR-6706-01 COSM4107939 c.1876G>A p.A626T Substitution - Missense 23:153910552-153910552 - TCGA-EE-A2MR-06 COSM3913639 c.696C>T p.F232F Substitution - coding silent 23:153919269-153919269 - ESCC-159T COSM3939867 c.2089C>T p.P697S Substitution - Missense 23:153910238-153910238 - 49M COSM5589711 c.1908C>T p.F636F Substitution - coding silent 23:153910520-153910520 - TCGA-14-0813 COSM1117664 c.1001G>A p.R334H Substitution - Missense 23:153918863-153918863 - TCGA-CG-4442-01 COSM4107937 c.1962C>T p.Y654Y Substitution - coding silent 23:153910365-153910365 - PCSI_0083_Pa_X COSM3379572 c.1542+1G>A p.? Unknown 23:153912699-153912699 - NB-3270 COSM1283480 c.273-3_273-2insC p.? Unknown 23:153921529-153921530 - RK308_C01 COSM3747382 c.73C>T p.R25C Substitution - Missense 23:153921804-153921804 - CX-1 COSM3236357 c.1068C>G p.D356E Substitution - Missense 23:153913844-153913844 - TCGA-JX-A3Q0-01 COSM4824436 c.142G>C p.E48Q Substitution - Missense 23:153921735-153921735 - TCGA-66-2773-01 COSM755728 c.2795C>G p.S932* Substitution - Nonsense 23:153907775-153907775 - LUAD-S01341 COSM404280 c.2824A>C p.T942P Substitution - Missense 23:153907746-153907746 - TCGA-FE-A23A-01 COSM3372154 c.422G>C p.R141P Substitution - Missense 23:153921378-153921378 - PTC_441 COSM5957411 c.2059C>A p.L687I Substitution - Missense 23:153910268-153910268 - LAU149 COSM234410 c.2079G>A p.R693R Substitution - coding silent 23:153910248-153910248 - 2492701 COSM5599084 c.471C>T p.L157L Substitution - coding silent 23:153921124-153921124 - T3090 COSM4662930 c.1709C>T p.T570I Substitution - Missense 23:153910807-153910807 - ESCC_BICR_050T COSM5440140 c.850C>T p.L284F Substitution - Missense 23:153919014-153919014 - TCGA-AO-A03M-01 COSM3844022 c.1593C>G p.I531M Substitution - Missense 23:153911139-153911139 - CHC1731T COSM4792087 c.1356C>T p.S452S Substitution - coding silent 23:153913273-153913273 - S01861 COSM5671491 c.2287C>T p.Q763* Substitution - Nonsense 23:153909868-153909868 - TCGA-BH-A18G-01 COSM3844024 c.764C>T p.A255V Substitution - Missense 23:153919201-153919201 - TCGA-A6-6781-01 COSM1466662 c.1194C>T p.D398D Substitution - coding silent 23:153913541-153913541 - 08-P054 COSM4589291 c.726G>A p.A242A Substitution - coding silent 23:153919239-153919239 - OSCC-GB_00890111 COSM4887505 c.1325C>T p.T442M Substitution - Missense 23:153913410-153913410 - S02299 COSM5691036 c.2342G>A p.S781N Substitution - Missense 23:153909813-153909813 - TCGA-AJ-A23M-01 COSM1117673 c.116G>A p.G39D Substitution - Missense 23:153921761-153921761 - TCGA-NH-A5IV-01 COSM5184700 c.1868G>A p.R623Q Substitution - Missense 23:153910560-153910560 - SW620 COSM3236343 c.2063T>C p.I688T Substitution - Missense 23:153910264-153910264 - BHY COSM3236323 c.2303G>A p.R768Q Substitution - Missense 23:153909852-153909852 - TCGA-AC-A23H-01 COSM3844020 c.2382C>T p.L794L Substitution - coding silent 23:153909773-153909773 - S00356 COSM309245 c.2465G>T p.G822V Substitution - Missense 23:153909485-153909485 - CHEWS001 COSM4589287 c.2113G>A p.V705I Substitution - Missense 23:153910214-153910214 - YUKAT COSM5412310 c.1738G>A p.V580M Substitution - Missense 23:153910778-153910778 - CSCC-38-T COSM4516158 c.1516_1517GG>AA p.G506K Substitution - Missense 23:153912725-153912726 - Br27P COSM39848 c.102C>T p.C34C Substitution - coding silent 23:153921775-153921775 - TCGA-BR-4362-01 COSM4107941 c.837C>A p.A279A Substitution - coding silent 23:153919027-153919027 - T3174 COSM4662920 c.2809delC p.Q937fs*3 Deletion - Frameshift 23:153907761-153907761 - PCSI_0136_Pa_X COSM1557077 c.1000C>T p.R334C Substitution - Missense 23:153918864-153918864 - AOCS-064-1-6 COSM4137762 c.2804A>C p.H935P Substitution - Missense 23:153907766-153907766 - TCGA-AP-A056-01 COSM1117659 c.1530G>T p.E510D Substitution - Missense 23:153912712-153912712 - PCSI_0083_Pa_P_526 COSM3379572 c.1542+1G>A p.? Unknown 23:153912699-153912699 - TCGA-FW-A3R5-06 COSM3913637 c.2542C>T p.P848S Substitution - Missense 23:153909135-153909135 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.701274;Hs.701275;Hs.701288;Hs.701291;Hs.701297;Hs.701302;Hs.701305;Hs.701308;Hs.701316;Hs.701319;Hs.701321;Hs.701324 Xq28 300023

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer C A IntronicSNV . c.1663-44G>T X 153176687 CLL C A Missense p.G862V c.2585G>T X 153174939 SCLC C A Synonymous p.L37L c.111G>T X 153187219 PRAD C A Synonymous p.V850V c.2550G>T X 153174974 BRCA C G Missense p.D980H c.2938G>C X 153173206 LUAD C G Missense p.R141P c.422G>C X 153186831 THCA C G Missense p.R65P c.194G>C X 153187136 STAD C T Missense p.A666T c.1996G>A X 153176006 STAD C T Missense p.A780T c.2338G>A X 153175478 UCEC C T Missense p.D148N c.442G>A X 153186606 CM C T Missense p.D548N c.1642G>A X 153178174 HNSC C T Missense p.G39D c.116G>A X 153187214 UCEC C T Missense p.G439R c.1315G>A X 153178994 HNSC C T Missense p.R374H c.1121G>A X 153184317 GBM C T Missense p.R595H c.1784G>A X 153176393 UCEC C T Missense p.V698M c.2092G>A X 153175809 GBM C T Synonymous p.C34C c.102C>T X 153187228 GBM C T Synonymous p.L855L c.2565G>A X 153174959 UCEC C T Synonymous p.P752P c.2256G>A X 153175645 STAD C T Synonymous p.Q730Q c.2190G>A X 153175711 STAD C T Synonymous p.T166T c.498G>A X 153186550 CM C T Synonymous p.T170T c.510G>A X 153186251 HNSC G A Missense p.R141C c.421C>T X 153186832 NSCLC G A Missense p.T170M c.509C>T X 153186252 LUAD G A Missense p.T478I c.1433C>T X 153178876 CM G A Synonymous p.D760D c.2280C>T X 153175536 LGG G A Synonymous p.F638F c.1914C>T X 153176176 CM G A Synonymous p.L345L c.1033C>T X 153184405 CM G A Synonymous p.L7L c.19C>T X 153191638 CM G C Missense p.S936C c.2807C>G X 153173337 LUSC G C Nonsense p.S972* c.2915C>G X 153173229 LUSC G C Synonymous p.L544L c.1632C>G X 153178184 HNSC GG TA Synonymous p.(=) c.2421_2422delinsTA X 153175307 CM T A Missense p.K527N c.1581A>T X 153178235 UCEC T A Missense p.S117C c.349A>T X 153186904 HNSC TC CT Missense p.E747R c.2239_2240delinsAG X 153175661 CM T C Missense p.D811G c.2432A>G X 153175297 HNSC T C Missense p.T170A c.508A>G X 153186253 SCLC T G Missense p.D313A c.938A>C X 153184500 UCEC T G Missense p.Q730P c.2189A>C X 153175712 CM