Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 4 146058671 146058671 + Missense_Mutation SNP G G C TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr4:146058671G>C c.3256C>G c.(3256-3258)Cag>Gag p.Q1086E BLCA 4 146058794 146058794 + Nonsense_Mutation SNP G G A TCGA-FJ-A3ZF-01A-11D-A23M-08 TCGA-FJ-A3ZF-10A-01D-A23K-08 g.chr4:146058794G>A c.3133C>T c.(3133-3135)Caa>Taa p.Q1045* BLCA 4 146059082 146059082 + Missense_Mutation SNP C C T TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr4:146059082C>T c.2845G>A c.(2845-2847)Gca>Aca p.A949T BLCA 4 146059592 146059592 + Missense_Mutation SNP G G C TCGA-FD-A5BX-01A-11D-A26M-08 TCGA-FD-A5BX-10A-01D-A26K-08 g.chr4:146059592G>C c.2335C>G c.(2335-2337)Caa>Gaa p.Q779E BLCA 4 146063358 146063358 + Silent SNP A A G TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr4:146063358A>G c.1812T>C c.(1810-1812)ttT>ttC p.F604F BLCA 4 146067481 146067481 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:146067481C>T c.1360G>A c.(1360-1362)Gaa>Aaa p.E454K BLCA 4 146067508 146067508 + Missense_Mutation SNP C C T TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr4:146067508C>T c.1333G>A c.(1333-1335)Gaa>Aaa p.E445K BLCA 4 146071800 146071800 + Nonsense_Mutation SNP G G C TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr4:146071800G>C c.1124C>G c.(1123-1125)tCa>tGa p.S375* BLCA 4 146077090 146077090 + Missense_Mutation SNP C C T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr4:146077090C>T c.688G>A c.(688-690)Gag>Aag p.E230K BLCA 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-FD-A3B7-01A-31D-A20D-08 TCGA-FD-A3B7-10A-01D-A20D-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del BLCA 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del BRCA 4 146058902 146058902 + Missense_Mutation SNP C C T TCGA-D8-A27E-01A-11D-A16D-09 TCGA-D8-A27E-10A-01D-A16D-09 g.chr4:146058902C>T c.3025G>A c.(3025-3027)Gcc>Acc p.A1009T BRCA 4 146058951 146058953 + In_Frame_Del DEL TGT TGT - TCGA-AC-A5EI-01A-11D-A27P-09 TCGA-AC-A5EI-10A-01D-A27P-09 g.chr4:146058951_146058953delTGT c.2974_2976delACA c.(2974-2976)acadel p.T992del BRCA 4 146059245 146059245 + Silent SNP C C T TCGA-AO-A1KP-01A-11D-A13L-09 TCGA-AO-A1KP-10A-01W-A14R-09 g.chr4:146059245C>T c.2682G>A c.(2680-2682)ctG>ctA p.L894L BRCA 4 146059276 146059276 + Missense_Mutation SNP G G A TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr4:146059276G>A c.2651C>T c.(2650-2652)tCt>tTt p.S884F BRCA 4 146059425 146059425 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr4:146059425C>A c.2502G>T c.(2500-2502)aaG>aaT p.K834N BRCA 4 146062555 146062555 + Nonsense_Mutation SNP G G A TCGA-E2-A15R-01A-11D-A10Y-09 TCGA-E2-A15R-10A-01D-A110-09 g.chr4:146062555G>A c.2059C>T c.(2059-2061)Cag>Tag p.Q687* BRCA 4 146067547 146067547 + Missense_Mutation SNP G G A TCGA-BH-A1F8-01A-11D-A13L-09 TCGA-BH-A1F8-11B-21D-A188-09 g.chr4:146067547G>A c.1294C>T c.(1294-1296)Cac>Tac p.H432Y BRCA 4 146076763 146076763 + Missense_Mutation SNP A A G TCGA-A8-A07E-01A-11W-A050-09 TCGA-A8-A07E-10A-01W-A055-09 g.chr4:146076763A>G c.766T>C c.(766-768)Tat>Cat p.Y256H BRCA 4 146076764 146076764 + Silent SNP G G C TCGA-AN-A0AM-01A-11W-A050-09 TCGA-AN-A0AM-10A-01W-A055-09 g.chr4:146076764G>C c.765C>G c.(763-765)gtC>gtG p.V255V CESC 4 146058813 146058813 + Missense_Mutation SNP T T A TCGA-FU-A23L-01A-11D-A16O-08 TCGA-FU-A23L-10A-01D-A16O-08 g.chr4:146058813T>A c.3114A>T c.(3112-3114)agA>agT p.R1038S CESC 4 146059410 146059410 + Silent SNP C C T TCGA-C5-A1BF-01B-11D-A13W-08 TCGA-C5-A1BF-10A-01D-A13W-08 g.chr4:146059410C>T c.2517G>A c.(2515-2517)caG>caA p.Q839Q CESC 4 146065559 146065559 + Nonsense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr4:146065559G>A c.1450C>T c.(1450-1452)Cag>Tag p.Q484* CESC 4 146065567 146065567 + Missense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr4:146065567G>A c.1442C>T c.(1441-1443)tCa>tTa p.S481L CHOL 4 146065546 146065546 + Missense_Mutation SNP G G T TCGA-W5-AA2X-01A-11D-A417-09 TCGA-W5-AA2X-10A-01D-A41A-09 g.chr4:146065546G>T c.1463C>A c.(1462-1464)cCa>cAa p.P488Q COAD 4 146058598 146058598 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr4:146058598C>A c.3329G>T c.(3328-3330)aGg>aTg p.R1110M COAD 4 146058656 146058656 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:146058656C>A c.3271G>T c.(3271-3273)Gtc>Ttc p.V1091F COAD 4 146058661 146058661 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr4:146058661C>T c.3266G>A c.(3265-3267)cGa>cAa p.R1089Q COAD 4 146058661 146058661 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:146058661C>T c.3266G>A c.(3265-3267)cGa>cAa p.R1089Q COAD 4 146058727 146058727 + Missense_Mutation SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr4:146058727A>G c.3200T>C c.(3199-3201)gTg>gCg p.V1067A COAD 4 146058727 146058727 + Missense_Mutation SNP A A T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr4:146058727A>T c.3200T>A c.(3199-3201)gTg>gAg p.V1067E COAD 4 146058728 146058728 + Missense_Mutation SNP C C T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr4:146058728C>T c.3199G>A c.(3199-3201)Gtg>Atg p.V1067M COAD 4 146058810 146058810 + Silent SNP G G A TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr4:146058810G>A c.3117C>T c.(3115-3117)tcC>tcT p.S1039S COAD 4 146058810 146058810 + Silent SNP G G T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr4:146058810G>T c.3117C>A c.(3115-3117)tcC>tcA p.S1039S COAD 4 146058811 146058811 + Missense_Mutation SNP G G A TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr4:146058811G>A c.3116C>T c.(3115-3117)tCc>tTc p.S1039F COAD 4 146058811 146058811 + Missense_Mutation SNP G G T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr4:146058811G>T c.3116C>A c.(3115-3117)tCc>tAc p.S1039Y COAD 4 146059009 146059010 + Frame_Shift_Del DEL TC TC - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:146059009_146059010delTC c.2917_2918delGA c.(2917-2919)gaafs p.E973fs COAD 4 146059018 146059018 + Missense_Mutation SNP C C G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr4:146059018C>G c.2909G>C c.(2908-2910)aGa>aCa p.R970T COAD 4 146059158 146059158 + Silent SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr4:146059158G>A c.2769C>T c.(2767-2769)ctC>ctT p.L923L COAD 4 146059216 146059216 + Missense_Mutation SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr4:146059216C>T c.2711G>A c.(2710-2712)gGt>gAt p.G904D COAD 4 146059566 146059566 + Silent SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr4:146059566C>T c.2361G>A c.(2359-2361)ccG>ccA p.P787P COAD 4 146062619 146062619 + Silent SNP G G C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr4:146062619G>C c.1995C>G c.(1993-1995)ctC>ctG p.L665L COAD 4 146062645 146062645 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:146062645T>C c.1969A>G c.(1969-1971)Aca>Gca p.T657A COAD 4 146065474 146065474 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:146065474C>T c.1535G>A c.(1534-1536)cGa>cAa p.R512Q COAD 4 146067436 146067436 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr4:146067436C>T c.1405G>A c.(1405-1407)Gct>Act p.A469T COAD 4 146067471 146067471 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr4:146067471C>T c.1370G>A c.(1369-1371)cGt>cAt p.R457H COAD 4 146067563 146067563 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:146067563T>A c.1278A>T c.(1276-1278)agA>agT p.R426S COAD 4 146071829 146071829 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:146071829C>A c.1095G>T c.(1093-1095)aaG>aaT p.K365N COAD 4 146073755 146073755 + Silent SNP A A G TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr4:146073755A>G c.906T>C c.(904-906)aaT>aaC p.N302N COAD 4 146073789 146073789 + Splice_Site SNP T T C TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr4:146073789T>C c.e11-2 COAD 4 146076741 146076741 + Missense_Mutation SNP A A T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr4:146076741A>T c.788T>A c.(787-789)aTt>aAt p.I263N COAD 4 146076751 146076751 + Nonsense_Mutation SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr4:146076751C>A c.778G>T c.(778-780)Gaa>Taa p.E260* COADREAD 4 146058598 146058598 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr4:146058598C>A c.3329G>T c.(3328-3330)aGg>aTg p.R1110M COADREAD 4 146058656 146058656 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:146058656C>A c.3271G>T c.(3271-3273)Gtc>Ttc p.V1091F COADREAD 4 146058661 146058661 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr4:146058661C>T c.3266G>A c.(3265-3267)cGa>cAa p.R1089Q COADREAD 4 146058661 146058661 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:146058661C>T c.3266G>A c.(3265-3267)cGa>cAa p.R1089Q COADREAD 4 146058727 146058727 + Missense_Mutation SNP A A G TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr4:146058727A>G c.3200T>C c.(3199-3201)gTg>gCg p.V1067A COADREAD 4 146058727 146058727 + Missense_Mutation SNP A A T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr4:146058727A>T c.3200T>A c.(3199-3201)gTg>gAg p.V1067E COADREAD 4 146058728 146058728 + Missense_Mutation SNP C C T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr4:146058728C>T c.3199G>A c.(3199-3201)Gtg>Atg p.V1067M COADREAD 4 146058810 146058810 + Silent SNP G G A TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr4:146058810G>A c.3117C>T c.(3115-3117)tcC>tcT p.S1039S COADREAD 4 146058810 146058810 + Silent SNP G G T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr4:146058810G>T c.3117C>A c.(3115-3117)tcC>tcA p.S1039S COADREAD 4 146058811 146058811 + Missense_Mutation SNP G G A TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr4:146058811G>A c.3116C>T c.(3115-3117)tCc>tTc p.S1039F COADREAD 4 146058811 146058811 + Missense_Mutation SNP G G T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr4:146058811G>T c.3116C>A c.(3115-3117)tCc>tAc p.S1039Y COADREAD 4 146059009 146059010 + Frame_Shift_Del DEL TC TC - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr4:146059009_146059010delTC c.2917_2918delGA c.(2917-2919)gaafs p.E973fs COADREAD 4 146059018 146059018 + Missense_Mutation SNP C C G TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr4:146059018C>G c.2909G>C c.(2908-2910)aGa>aCa p.R970T COADREAD 4 146059158 146059158 + Silent SNP G G A TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr4:146059158G>A c.2769C>T c.(2767-2769)ctC>ctT p.L923L COADREAD 4 146059216 146059216 + Missense_Mutation SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr4:146059216C>T c.2711G>A c.(2710-2712)gGt>gAt p.G904D COADREAD 4 146059566 146059566 + Silent SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr4:146059566C>T c.2361G>A c.(2359-2361)ccG>ccA p.P787P COADREAD 4 146062619 146062619 + Silent SNP G G C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr4:146062619G>C c.1995C>G c.(1993-1995)ctC>ctG p.L665L COADREAD 4 146062645 146062645 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr4:146062645T>C c.1969A>G c.(1969-1971)Aca>Gca p.T657A COADREAD 4 146065474 146065474 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:146065474C>T c.1535G>A c.(1534-1536)cGa>cAa p.R512Q COADREAD 4 146067436 146067436 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr4:146067436C>T c.1405G>A c.(1405-1407)Gct>Act p.A469T COADREAD 4 146067471 146067471 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr4:146067471C>T c.1370G>A c.(1369-1371)cGt>cAt p.R457H COADREAD 4 146067563 146067563 + Missense_Mutation SNP T T A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:146067563T>A c.1278A>T c.(1276-1278)agA>agT p.R426S COADREAD 4 146071829 146071829 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr4:146071829C>A c.1095G>T c.(1093-1095)aaG>aaT p.K365N COADREAD 4 146072024 146072024 + Silent SNP T T G TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr4:146072024T>G c.1002A>C c.(1000-1002)ccA>ccC p.P334P COADREAD 4 146073755 146073755 + Silent SNP A A G TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr4:146073755A>G c.906T>C c.(904-906)aaT>aaC p.N302N COADREAD 4 146073789 146073789 + Splice_Site SNP T T C TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr4:146073789T>C c.e11-2 COADREAD 4 146076741 146076741 + Missense_Mutation SNP A A T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr4:146076741A>T c.788T>A c.(787-789)aTt>aAt p.I263N COADREAD 4 146076751 146076751 + Nonsense_Mutation SNP C C A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr4:146076751C>A c.778G>T c.(778-780)Gaa>Taa p.E260* COADREAD 4 146092862 146092862 + Missense_Mutation SNP C C G TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr4:146092862C>G c.254G>C c.(253-255)gGa>gCa p.G85A DLBC 4 146059393 146059393 + Missense_Mutation SNP T T C TCGA-VB-A8QN-01A-11D-A382-10 TCGA-VB-A8QN-10A-01D-A385-10 g.chr4:146059393T>C c.2534A>G c.(2533-2535)aAt>aGt p.N845S DLBC 4 146063471 146063471 + Missense_Mutation SNP C C T TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr4:146063471C>T c.1699G>A c.(1699-1701)Gtg>Atg p.V567M ESCA 4 146059597 146059597 + Missense_Mutation SNP T T A TCGA-IG-A3I8-01A-11D-A247-09 TCGA-IG-A3I8-10A-01D-A247-09 g.chr4:146059597T>A c.2330A>T c.(2329-2331)aAt>aTt p.N777I ESCA 4 146064566 146064566 + Missense_Mutation SNP G G A TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr4:146064566G>A c.1634C>T c.(1633-1635)tCa>tTa p.S545L ESCA 4 146077125 146077125 + Missense_Mutation SNP G G T TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chr4:146077125G>T c.653C>A c.(652-654)gCt>gAt p.A218D ESCA 4 146085307 146085307 + Splice_Site DEL T T - TCGA-V5-A7RE-01A-11D-A351-09 TCGA-V5-A7RE-10A-01D-A351-09 g.chr4:146085307delT c.413delA c.(412-414)aag>ag p.K138fs ESCA 4 146095823 146095823 + Missense_Mutation SNP T T C TCGA-Z6-A8JE-01A-11D-A37C-09 TCGA-Z6-A8JE-10A-01D-A37F-09 g.chr4:146095823T>C c.233A>G c.(232-234)aAa>aGa p.K78R GBM 4 146059760 146059760 + Missense_Mutation SNP G G A TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr4:146059760G>A c.2167C>T c.(2167-2169)Cct>Tct p.P723S GBM 4 146077118 146077118 + Silent SNP C C T TCGA-06-0216-01B-01D-1492-08 TCGA-06-0216-10A-01D-1492-08 g.chr4:146077118C>T c.660G>A c.(658-660)gtG>gtA p.V220V GBMLGG 4 146058891 146058891 + Silent SNP A A C TCGA-HT-7688-01A-11D-2253-08 TCGA-HT-7688-10A-01D-2253-08 g.chr4:146058891A>C c.3036T>G c.(3034-3036)gtT>gtG p.V1012V GBMLGG 4 146059313 146059313 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146059313C>T c.2614G>A c.(2614-2616)Gaa>Aaa p.E872K GBMLGG 4 146059760 146059760 + Missense_Mutation SNP G G A TCGA-32-2634-01A-01D-1495-08 TCGA-32-2634-10A-01D-1495-08 g.chr4:146059760G>A c.2167C>T c.(2167-2169)Cct>Tct p.P723S GBMLGG 4 146067419 146067419 + Splice_Site SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146067419G>A c.1422C>T c.(1420-1422)tcC>tcT p.S474S GBMLGG 4 146077118 146077118 + Silent SNP C C T TCGA-06-0216-01B-01D-1492-08 TCGA-06-0216-10A-01D-1492-08 g.chr4:146077118C>T c.660G>A c.(658-660)gtG>gtA p.V220V GBMLGG 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-HT-7470-01A-12D-2086-08 TCGA-HT-7470-10A-01D-2086-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del GBMLGG 4 146092833 146092833 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146092833C>T c.283G>A c.(283-285)Gaa>Aaa p.E95K HNSC 4 146059009 146059010 + Frame_Shift_Del DEL TC TC - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr4:146059009_146059010delTC c.2917_2918delGA c.(2917-2919)gaafs p.E973fs HNSC 4 146059150 146059150 + Missense_Mutation SNP G G T TCGA-BA-5559-01A-01D-1512-08 TCGA-BA-5559-10A-01D-1512-08 g.chr4:146059150G>T c.2777C>A c.(2776-2778)gCa>gAa p.A926E HNSC 4 146059380 146059380 + Silent SNP G G A TCGA-CQ-A4C6-01A-11D-A25D-08 TCGA-CQ-A4C6-10A-01D-A25E-08 g.chr4:146059380G>A c.2547C>T c.(2545-2547)ggC>ggT p.G849G HNSC 4 146064571 146064571 + Silent SNP T T A TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chr4:146064571T>A c.1629A>T c.(1627-1629)acA>acT p.T543T HNSC 4 146071685 146071685 + Frame_Shift_Del DEL C C - TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr4:146071685delC c.1239delG c.(1237-1239)cggfs p.R413fs HNSC 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-WA-A7H4-01A-21D-A34J-08 TCGA-WA-A7H4-10A-01D-A34M-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del KIPAN 4 146063397 146063398 + Frame_Shift_Ins INS - - G TCGA-BP-4968-01A-01D-1462-08 TCGA-BP-4968-11A-01D-1462-08 g.chr4:146063397_146063398insG c.1772_1773insC c.(1771-1773)ccafs p.P591fs KIPAN 4 146063415 146063415 + Silent SNP A A T TCGA-2Z-A9JR-01A-12D-A42J-10 TCGA-2Z-A9JR-10A-01D-A42M-10 g.chr4:146063415A>T c.1755T>A c.(1753-1755)ccT>ccA p.P585P KIPAN 4 146063450 146063450 + Missense_Mutation SNP G G A TCGA-B0-5110-01A-01D-1421-08 TCGA-B0-5110-11A-01D-1421-08 g.chr4:146063450G>A c.1720C>T c.(1720-1722)Ccc>Tcc p.P574S KIPAN 4 146071985 146071985 + Missense_Mutation SNP T T A TCGA-UZ-A9PM-01A-21D-A382-10 TCGA-UZ-A9PM-10A-01D-A385-10 g.chr4:146071985T>A c.1041A>T c.(1039-1041)aaA>aaT p.K347N KIPAN 4 146076739 146076739 + Frame_Shift_Del DEL A A - TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr4:146076739delA c.790delT c.(790-792)tggfs p.W264fs KIPAN 4 146076795 146076795 + Missense_Mutation SNP C C A TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr4:146076795C>A c.734G>T c.(733-735)aGa>aTa p.R245I KIRC 4 146063397 146063398 + Frame_Shift_Ins INS - - G TCGA-BP-4968-01A-01D-1462-08 TCGA-BP-4968-11A-01D-1462-08 g.chr4:146063397_146063398insG c.1772_1773insC c.(1771-1773)ccafs p.P591fs KIRC 4 146063450 146063450 + Missense_Mutation SNP G G A TCGA-B0-5110-01A-01D-1421-08 TCGA-B0-5110-11A-01D-1421-08 g.chr4:146063450G>A c.1720C>T c.(1720-1722)Ccc>Tcc p.P574S KIRC 4 146076739 146076739 + Frame_Shift_Del DEL A A - TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chr4:146076739delA c.790delT c.(790-792)tggfs p.W264fs KIRP 4 146063415 146063415 + Silent SNP A A T TCGA-2Z-A9JR-01A-12D-A42J-10 TCGA-2Z-A9JR-10A-01D-A42M-10 g.chr4:146063415A>T c.1755T>A c.(1753-1755)ccT>ccA p.P585P KIRP 4 146071985 146071985 + Missense_Mutation SNP T T A TCGA-UZ-A9PM-01A-21D-A382-10 TCGA-UZ-A9PM-10A-01D-A385-10 g.chr4:146071985T>A c.1041A>T c.(1039-1041)aaA>aaT p.K347N KIRP 4 146076795 146076795 + Missense_Mutation SNP C C A TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr4:146076795C>A c.734G>T c.(733-735)aGa>aTa p.R245I LGG 4 146058891 146058891 + Silent SNP A A C TCGA-HT-7688-01A-11D-2253-08 TCGA-HT-7688-10A-01D-2253-08 g.chr4:146058891A>C c.3036T>G c.(3034-3036)gtT>gtG p.V1012V LGG 4 146059313 146059313 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146059313C>T c.2614G>A c.(2614-2616)Gaa>Aaa p.E872K LGG 4 146067419 146067419 + Splice_Site SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146067419G>A c.1422C>T c.(1420-1422)tcC>tcT p.S474S LGG 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-HT-7470-01A-12D-2086-08 TCGA-HT-7470-10A-01D-2086-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del LGG 4 146092833 146092833 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:146092833C>T c.283G>A c.(283-285)Gaa>Aaa p.E95K LUAD 4 146058708 146058708 + Missense_Mutation SNP C C A TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr4:146058708C>A c.3219G>T c.(3217-3219)tgG>tgT p.W1073C LUAD 4 146059084 146059085 + Frame_Shift_Ins INS - - T TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr4:146059084_146059085insT c.2842_2843insA c.(2842-2844)acgfs p.T948fs LUAD 4 146059096 146059096 + Missense_Mutation SNP C C T TCGA-75-5125-01A-01D-1753-08 TCGA-75-5125-10A-01D-1753-08 g.chr4:146059096C>T c.2831G>A c.(2830-2832)cGa>cAa p.R944Q LUAD 4 146063380 146063380 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr4:146063380C>A c.1790G>T c.(1789-1791)tGg>tTg p.W597L LUAD 4 146067520 146067520 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr4:146067520C>A c.1321G>T c.(1321-1323)Ggc>Tgc p.G441C LUAD 4 146071687 146071687 + Missense_Mutation SNP G G A TCGA-17-Z042-01A-01W-0746-08 TCGA-17-Z042-11A-01W-0746-08 g.chr4:146071687G>A c.1237C>T c.(1237-1239)Cgg>Tgg p.R413W LUAD 4 146077104 146077104 + Missense_Mutation SNP G G C TCGA-50-5072-01A-21D-1855-08 TCGA-50-5072-10A-01D-1855-08 g.chr4:146077104G>C c.674C>G c.(673-675)cCt>cGt p.P225R LUSC 4 146064527 146064527 + Missense_Mutation SNP G G A TCGA-56-5898-01A-11D-1632-08 TCGA-56-5898-10A-01D-1632-08 g.chr4:146064527G>A c.1673C>T c.(1672-1674)cCt>cTt p.P558L LUSC 4 146067571 146067571 + Missense_Mutation SNP G G C TCGA-22-4591-01A-01D-1267-08 TCGA-22-4591-11A-01D-1267-08 g.chr4:146067571G>C c.1270C>G c.(1270-1272)Cgt>Ggt p.R424G LUSC 4 146073750 146073750 + Missense_Mutation SNP T T A TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr4:146073750T>A c.911A>T c.(910-912)gAt>gTt p.D304V LUSC 4 146080657 146080657 + Missense_Mutation SNP G G C TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr4:146080657G>C c.627C>G c.(625-627)tgC>tgG p.C209W OV 4 146058728 146058728 + Missense_Mutation SNP C C A TCGA-24-2281-01A-01W-0799-08 TCGA-24-2281-10A-01W-0799-08 g.chr4:146058728C>A c.3199G>T c.(3199-3201)Gtg>Ttg p.V1067L OV 4 146058812 146058812 + Missense_Mutation SNP A A C TCGA-10-0930-01A-02W-0421-09 TCGA-10-0930-11A-01W-0977-09 g.chr4:146058812A>C c.3115T>G c.(3115-3117)Tcc>Gcc p.S1039A OV 4 146092822 146092822 + Splice_Site SNP C C A TCGA-24-1556-01A-01W-0615-10 TCGA-24-1556-10A-01W-0615-10 g.chr4:146092822C>A c.294G>T c.(292-294)caG>caT p.Q98H PAAD 4 146058757 146058757 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:146058757C>T c.3170G>A c.(3169-3171)gGc>gAc p.G1057D PAAD 4 146058966 146058966 + Silent SNP G G A TCGA-YH-A8SY-01A-11D-A377-08 TCGA-YH-A8SY-10A-01D-A37A-08 g.chr4:146058966G>A c.2961C>T c.(2959-2961)agC>agT p.S987S PAAD 4 146064545 146064545 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr4:146064545T>G c.1655A>C c.(1654-1656)aAg>aCg p.K552T PAAD 4 146073752 146073752 + Silent SNP T T A TCGA-LB-A7SX-01A-11D-A33T-08 TCGA-LB-A7SX-10A-01D-A33W-08 g.chr4:146073752T>A c.909A>T c.(907-909)gcA>gcT p.A303A PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-3A-A9IB-01A-21D-A397-08 TCGA-3A-A9IB-10A-01D-A39A-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-3A-A9IH-01A-12D-A397-08 TCGA-3A-A9IH-10A-01D-A39A-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-3A-A9IU-01A-11D-A397-08 TCGA-3A-A9IU-10A-01D-A39A-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-3A-A9IV-01A-11D-A40W-08 TCGA-3A-A9IV-10A-01D-A40W-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-3A-A9J0-01A-11D-A40W-08 TCGA-3A-A9J0-10A-01D-A40W-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-HZ-7925-01A-11D-2154-08 TCGA-HZ-7925-10A-01D-2154-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-IB-A5SP-01A-11D-A32N-08 TCGA-IB-A5SP-10A-01D-A32N-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-IB-A5SQ-01A-11D-A32N-08 TCGA-IB-A5SQ-10A-01D-A32N-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-IB-A7M4-01A-11D-A36O-08 TCGA-IB-A7M4-10A-01D-A367-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-Q3-A5QY-01A-12D-A32N-08 TCGA-Q3-A5QY-10A-01D-A32N-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-Q3-AA2A-01A-11D-A377-08 TCGA-Q3-AA2A-10A-01D-A37A-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-RB-A7B8-01A-12D-A33T-08 TCGA-RB-A7B8-10A-01D-A33W-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-US-A776-01A-13D-A33T-08 TCGA-US-A776-11A-11D-A33W-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-XD-AAUH-01A-42D-A40W-08 TCGA-XD-AAUH-11A-11D-A40W-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PAAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-XD-AAUL-01A-21D-A397-08 TCGA-XD-AAUL-10A-01D-A39A-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PRAD 4 146058591 146058591 + Silent SNP C C T TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr4:146058591C>T c.3336G>A c.(3334-3336)caG>caA p.Q1112Q PRAD 4 146058804 146058804 + Missense_Mutation SNP C C A TCGA-CH-5766-01A-11D-1576-08 TCGA-CH-5766-11A-01D-1576-08 g.chr4:146058804C>A c.3123G>T c.(3121-3123)caG>caT p.Q1041H PRAD 4 146058891 146058891 + Silent SNP A A C TCGA-FC-7708-01A-11D-2114-08 TCGA-FC-7708-10A-01D-2115-08 g.chr4:146058891A>C c.3036T>G c.(3034-3036)gtT>gtG p.V1012V PRAD 4 146067543 146067543 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr4:146067543G>A c.1298C>T c.(1297-1299)aCa>aTa p.T433I PRAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-EJ-5531-01A-01D-1576-08 TCGA-EJ-5531-10A-01D-1577-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del PRAD 4 146077123 146077125 + In_Frame_Del DEL CAG CAG - TCGA-HC-7738-01A-11D-2114-08 TCGA-HC-7738-10A-01D-2115-08 g.chr4:146077123_146077125delCAG c.653_655delCTG c.(652-657)gctgat>gat p.A218del READ 4 146072024 146072024 + Silent SNP T T G TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr4:146072024T>G c.1002A>C c.(1000-1002)ccA>ccC p.P334P READ 4 146092862 146092862 + Missense_Mutation SNP C C G TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr4:146092862C>G c.254G>C c.(253-255)gGa>gCa p.G85A SKCM 4 146062615 146062615 + Missense_Mutation SNP G G A TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr4:146062615G>A c.1999C>T c.(1999-2001)Cct>Tct p.P667S SKCM 4 146064533 146064533 + Missense_Mutation SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr4:146064533G>A c.1667C>T c.(1666-1668)cCt>cTt p.P556L SKCM 4 146065533 146065533 + Silent SNP T T C TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr4:146065533T>C c.1476A>G c.(1474-1476)agA>agG p.R492R SKCM 4 146065546 146065546 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr4:146065546G>A c.1463C>T c.(1462-1464)cCa>cTa p.P488L SKCM 4 146067419 146067419 + Splice_Site SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr4:146067419G>A c.1422C>T c.(1420-1422)tcC>tcT p.S474S SKCM 4 146067531 146067531 + Missense_Mutation SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr4:146067531G>A c.1310C>T c.(1309-1311)tCt>tTt p.S437F SKCM 4 146071734 146071734 + Nonsense_Mutation SNP G G C TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr4:146071734G>C c.1190C>G c.(1189-1191)tCa>tGa p.S397* SKCM 4 146071980 146071980 + Missense_Mutation SNP G G A TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr4:146071980G>A c.1046C>T c.(1045-1047)tCc>tTc p.S349F SKCM 4 146072028 146072028 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr4:146072028G>A c.998C>T c.(997-999)cCc>cTc p.P333L SKCM 4 146076605 146076605 + Silent SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr4:146076605G>A c.831C>T c.(829-831)tcC>tcT p.S277S SKCM 4 146092826 146092826 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr4:146092826G>A c.290C>T c.(289-291)cCa>cTa p.P97L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 4 146065510 146065510 single base substitution C T downstream_gene_variant BLCA-CN 4 146065510 146065510 single base substitution C T exon_variant BLCA-CN 4 146065510 146065510 single base substitution C T missense_variant R435K 1304G>A BLCA-CN 4 146065510 146065510 single base substitution C T missense_variant R500K 1499G>A BLCA-US 4 146046206 146046206 single base substitution G A intron_variant BLCA-US 4 146058794 146058794 single base substitution G A intron_variant BLCA-US 4 146058794 146058794 single base substitution G A stop_gained Q1045* 3133C>T BLCA-US 4 146058794 146058794 single base substitution G A stop_gained Q980* 2938C>T BLCA-US 4 146059006 146059006 single base substitution G A intron_variant BLCA-US 4 146059006 146059006 single base substitution G A missense_variant T909I 2726C>T BLCA-US 4 146059006 146059006 single base substitution G A missense_variant T974I 2921C>T BLCA-US 4 146059041 146059041 single base substitution A G intron_variant BLCA-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C BLCA-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C BLCA-US 4 146063358 146063358 single base substitution A G downstream_gene_variant BLCA-US 4 146063358 146063358 single base substitution A G exon_variant BLCA-US 4 146063358 146063358 single base substitution A G synonymous_variant F539F 1617T>C BLCA-US 4 146063358 146063358 single base substitution A G synonymous_variant F604F 1812T>C BLCA-US 4 146067481 146067481 single base substitution C T downstream_gene_variant BLCA-US 4 146067481 146067481 single base substitution C T exon_variant BLCA-US 4 146067481 146067481 single base substitution C T missense_variant E389K 1165G>A BLCA-US 4 146067481 146067481 single base substitution C T missense_variant E454K 1360G>A BLCA-US 4 146067508 146067508 single base substitution C T downstream_gene_variant BLCA-US 4 146067508 146067508 single base substitution C T exon_variant BLCA-US 4 146067508 146067508 single base substitution C T missense_variant E380K 1138G>A BLCA-US 4 146067508 146067508 single base substitution C T missense_variant E445K 1333G>A BLCA-US 4 146071800 146071800 single base substitution G C exon_variant BLCA-US 4 146071800 146071800 single base substitution G C stop_gained S309* 926C>G BLCA-US 4 146071800 146071800 single base substitution G C stop_gained S310* 929C>G BLCA-US 4 146071800 146071800 single base substitution G C stop_gained S375* 1124C>G BLCA-US 4 146077090 146077090 single base substitution C T downstream_gene_variant BLCA-US 4 146077090 146077090 single base substitution C T missense_variant E165K 493G>A BLCA-US 4 146077090 146077090 single base substitution C T missense_variant E230K 688G>A BLCA-US 4 146077090 146077090 single base substitution C T splice_region_variant BLCA-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD153D BLCA-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD218D BLCA-US 4 146077123 146077125 deletion of <=200bp CAG - downstream_gene_variant BLCA-US 4 146077123 146077125 deletion of <=200bp CAG - exon_variant BOCA-FR 4 146077077 146077077 single base substitution A T downstream_gene_variant BOCA-FR 4 146077077 146077077 single base substitution A T intron_variant BOCA-FR 4 146103662 146103662 single base substitution C G upstream_gene_variant BRCA-EU 4 146028879 146028879 single base substitution T A downstream_gene_variant BRCA-EU 4 146030335 146030335 single base substitution T C downstream_gene_variant BRCA-EU 4 146031531 146031531 single base substitution C T downstream_gene_variant BRCA-EU 4 146037204 146037204 single base substitution G C intron_variant BRCA-EU 4 146037525 146037525 single base substitution A C intron_variant BRCA-EU 4 146040075 146040075 single base substitution C T intron_variant BRCA-EU 4 146040207 146040207 single base substitution C A intron_variant BRCA-EU 4 146040436 146040436 insertion of <=200bp - TTTCA intron_variant BRCA-EU 4 146040728 146040728 single base substitution A G intron_variant BRCA-EU 4 146041561 146041561 deletion of <=200bp T - intron_variant BRCA-EU 4 146042282 146042282 single base substitution G A intron_variant BRCA-EU 4 146043024 146043024 insertion of <=200bp - A intron_variant BRCA-EU 4 146043034 146043034 single base substitution A T intron_variant BRCA-EU 4 146044085 146044085 single base substitution T G intron_variant BRCA-EU 4 146044959 146044959 insertion of <=200bp - ATAAAAAGCTGTAGGCCACAGC intron_variant BRCA-EU 4 146045516 146045516 single base substitution T A intron_variant BRCA-EU 4 146045525 146045525 single base substitution G C intron_variant BRCA-EU 4 146046170 146046170 single base substitution A G intron_variant BRCA-EU 4 146046693 146046693 single base substitution G C intron_variant BRCA-EU 4 146048209 146048209 single base substitution C T intron_variant BRCA-EU 4 146048779 146048779 insertion of <=200bp - T intron_variant BRCA-EU 4 146049045 146049045 single base substitution G A intron_variant BRCA-EU 4 146049370 146049370 insertion of <=200bp - A intron_variant BRCA-EU 4 146050799 146050799 deletion of <=200bp G - downstream_gene_variant BRCA-EU 4 146050799 146050799 deletion of <=200bp G - intron_variant BRCA-EU 4 146054080 146054080 single base substitution A C downstream_gene_variant BRCA-EU 4 146054080 146054080 single base substitution A C intron_variant BRCA-EU 4 146054189 146054189 single base substitution A G downstream_gene_variant BRCA-EU 4 146054189 146054189 single base substitution A G intron_variant BRCA-EU 4 146054631 146054631 single base substitution A G downstream_gene_variant BRCA-EU 4 146054631 146054631 single base substitution A G intron_variant BRCA-EU 4 146054924 146054924 single base substitution A C 3_prime_UTR_variant BRCA-EU 4 146054924 146054924 single base substitution A C downstream_gene_variant BRCA-EU 4 146054924 146054924 single base substitution A C intron_variant BRCA-EU 4 146055550 146055550 single base substitution G C 3_prime_UTR_variant BRCA-EU 4 146055550 146055550 single base substitution G C downstream_gene_variant BRCA-EU 4 146055550 146055550 single base substitution G C intron_variant BRCA-EU 4 146055902 146055902 single base substitution T G 3_prime_UTR_variant BRCA-EU 4 146055902 146055902 single base substitution T G downstream_gene_variant BRCA-EU 4 146055902 146055902 single base substitution T G intron_variant BRCA-EU 4 146058215 146058215 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 146058215 146058215 single base substitution A G downstream_gene_variant BRCA-EU 4 146058215 146058215 single base substitution A G intron_variant BRCA-EU 4 146059010 146059010 single base substitution C A intron_variant BRCA-EU 4 146059010 146059010 single base substitution C A stop_gained E908* 2722G>T BRCA-EU 4 146059010 146059010 single base substitution C A stop_gained E973* 2917G>T BRCA-EU 4 146060812 146060812 single base substitution A G intron_variant BRCA-EU 4 146060897 146060897 single base substitution C G intron_variant BRCA-EU 4 146061302 146061302 single base substitution A G intron_variant BRCA-EU 4 146062810 146062810 single base substitution G C downstream_gene_variant BRCA-EU 4 146062810 146062810 single base substitution G C intron_variant BRCA-EU 4 146063935 146063935 insertion of <=200bp - A downstream_gene_variant BRCA-EU 4 146063935 146063935 insertion of <=200bp - A intron_variant BRCA-EU 4 146067246 146067246 single base substitution G A downstream_gene_variant BRCA-EU 4 146067246 146067246 single base substitution G A exon_variant BRCA-EU 4 146067246 146067246 single base substitution G A intron_variant BRCA-EU 4 146068334 146068334 deletion of <=200bp A - intron_variant BRCA-EU 4 146069403 146069403 single base substitution G A intron_variant BRCA-EU 4 146071444 146071444 single base substitution A G intron_variant BRCA-EU 4 146071604 146071604 single base substitution G T intron_variant BRCA-EU 4 146074169 146074169 single base substitution G A downstream_gene_variant BRCA-EU 4 146074169 146074169 single base substitution G A intron_variant BRCA-EU 4 146074169 146074169 single base substitution G A upstream_gene_variant BRCA-EU 4 146076625 146076625 single base substitution G C downstream_gene_variant BRCA-EU 4 146076625 146076625 single base substitution G C missense_variant Q205E 613C>G BRCA-EU 4 146076625 146076625 single base substitution G C missense_variant Q206E 616C>G BRCA-EU 4 146076625 146076625 single base substitution G C missense_variant Q271E 811C>G BRCA-EU 4 146076625 146076625 single base substitution G C splice_region_variant BRCA-EU 4 146076625 146076625 single base substitution G C upstream_gene_variant BRCA-EU 4 146076734 146076734 single base substitution C T downstream_gene_variant BRCA-EU 4 146076734 146076734 single base substitution C T exon_variant BRCA-EU 4 146076734 146076734 single base substitution C T synonymous_variant L199L 597G>A BRCA-EU 4 146076734 146076734 single base substitution C T synonymous_variant L200L 600G>A BRCA-EU 4 146076734 146076734 single base substitution C T synonymous_variant L265L 795G>A BRCA-EU 4 146076734 146076734 single base substitution C T upstream_gene_variant BRCA-EU 4 146077234 146077234 single base substitution C T downstream_gene_variant BRCA-EU 4 146077234 146077234 single base substitution C T intron_variant BRCA-EU 4 146079314 146079314 single base substitution T C downstream_gene_variant BRCA-EU 4 146079314 146079314 single base substitution T C intron_variant BRCA-EU 4 146079722 146079722 single base substitution G C downstream_gene_variant BRCA-EU 4 146079722 146079722 single base substitution G C intron_variant BRCA-EU 4 146079728 146079728 single base substitution G C downstream_gene_variant BRCA-EU 4 146079728 146079728 single base substitution G C intron_variant BRCA-EU 4 146081323 146081323 single base substitution T G intron_variant BRCA-EU 4 146081379 146081379 single base substitution A G intron_variant BRCA-EU 4 146083252 146083252 single base substitution G C intron_variant BRCA-EU 4 146084486 146084486 single base substitution G T intron_variant BRCA-EU 4 146084734 146084734 insertion of <=200bp - T intron_variant BRCA-EU 4 146085218 146085218 single base substitution T A intron_variant BRCA-EU 4 146086806 146086806 single base substitution T C intron_variant BRCA-EU 4 146088247 146088247 single base substitution A G downstream_gene_variant BRCA-EU 4 146088247 146088247 single base substitution A G intron_variant BRCA-EU 4 146088711 146088711 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 146088711 146088711 deletion of <=200bp A - intron_variant BRCA-EU 4 146089707 146089707 deletion of <=200bp A - downstream_gene_variant BRCA-EU 4 146089707 146089707 deletion of <=200bp A - intron_variant BRCA-EU 4 146090983 146090983 single base substitution G C downstream_gene_variant BRCA-EU 4 146090983 146090983 single base substitution G C intron_variant BRCA-EU 4 146093121 146093121 single base substitution C G intron_variant BRCA-EU 4 146093121 146093121 single base substitution C G upstream_gene_variant BRCA-EU 4 146093255 146093255 single base substitution C G intron_variant BRCA-EU 4 146093255 146093255 single base substitution C G upstream_gene_variant BRCA-EU 4 146094479 146094479 single base substitution G A intron_variant BRCA-EU 4 146094479 146094479 single base substitution G A upstream_gene_variant BRCA-EU 4 146094922 146094922 single base substitution G C intron_variant BRCA-EU 4 146094922 146094922 single base substitution G C upstream_gene_variant BRCA-EU 4 146095367 146095367 single base substitution G C intron_variant BRCA-EU 4 146095367 146095367 single base substitution G C upstream_gene_variant BRCA-EU 4 146095615 146095615 single base substitution A T intron_variant BRCA-EU 4 146095615 146095615 single base substitution A T upstream_gene_variant BRCA-EU 4 146096578 146096578 deletion of <=200bp C - intron_variant BRCA-EU 4 146096578 146096578 deletion of <=200bp C - upstream_gene_variant BRCA-EU 4 146096938 146096938 single base substitution G A intron_variant BRCA-EU 4 146096938 146096938 single base substitution G A upstream_gene_variant BRCA-EU 4 146100185 146100185 single base substitution C T intron_variant BRCA-EU 4 146100185 146100185 single base substitution C T upstream_gene_variant BRCA-EU 4 146100262 146100262 single base substitution G A intron_variant BRCA-EU 4 146100262 146100262 single base substitution G A upstream_gene_variant BRCA-EU 4 146100751 146100751 single base substitution A G 5_prime_UTR_variant BRCA-EU 4 146100751 146100751 single base substitution A G exon_variant BRCA-EU 4 146100751 146100751 single base substitution A G intron_variant BRCA-EU 4 146100751 146100751 single base substitution A G upstream_gene_variant BRCA-EU 4 146102164 146102164 single base substitution G C upstream_gene_variant BRCA-EU 4 146102221 146102221 single base substitution A T upstream_gene_variant BRCA-EU 4 146103714 146103714 single base substitution C G upstream_gene_variant BRCA-EU 4 146104512 146104512 single base substitution A G upstream_gene_variant BRCA-EU 4 146105730 146105730 single base substitution A T upstream_gene_variant BRCA-FR 4 146048209 146048209 single base substitution C T intron_variant BRCA-FR 4 146054080 146054080 single base substitution A C downstream_gene_variant BRCA-FR 4 146054080 146054080 single base substitution A C intron_variant BRCA-FR 4 146055550 146055550 single base substitution G C 3_prime_UTR_variant BRCA-FR 4 146055550 146055550 single base substitution G C downstream_gene_variant BRCA-FR 4 146055550 146055550 single base substitution G C intron_variant BRCA-FR 4 146056332 146056332 single base substitution A G 3_prime_UTR_variant BRCA-FR 4 146056332 146056332 single base substitution A G downstream_gene_variant BRCA-FR 4 146056332 146056332 single base substitution A G intron_variant BRCA-FR 4 146061302 146061302 single base substitution A G intron_variant BRCA-FR 4 146086806 146086806 single base substitution T C intron_variant BRCA-FR 4 146105730 146105730 single base substitution A T upstream_gene_variant BRCA-UK 4 146028518 146028518 single base substitution G T downstream_gene_variant BRCA-UK 4 146037525 146037525 single base substitution A C intron_variant BRCA-UK 4 146062810 146062810 single base substitution G C downstream_gene_variant BRCA-UK 4 146062810 146062810 single base substitution G C intron_variant BRCA-UK 4 146070612 146070612 single base substitution G C intron_variant BRCA-UK 4 146071604 146071604 single base substitution G T intron_variant BRCA-UK 4 146094675 146094675 single base substitution G A intron_variant BRCA-UK 4 146094675 146094675 single base substitution G A upstream_gene_variant BRCA-UK 4 146104512 146104512 single base substitution A G upstream_gene_variant BRCA-US 4 146031530 146031530 single base substitution A G downstream_gene_variant BRCA-US 4 146032219 146032219 single base substitution A G exon_variant BRCA-US 4 146038513 146038513 single base substitution A G intron_variant BRCA-US 4 146042543 146042543 insertion of <=200bp - A intron_variant BRCA-US 4 146044698 146044698 single base substitution C T intron_variant BRCA-US 4 146048720 146048720 single base substitution G T intron_variant BRCA-US 4 146058902 146058902 single base substitution C T intron_variant BRCA-US 4 146058902 146058902 single base substitution C T missense_variant A1009T 3025G>A BRCA-US 4 146058902 146058902 single base substitution C T missense_variant A944T 2830G>A BRCA-US 4 146059245 146059245 single base substitution C T intron_variant BRCA-US 4 146059245 146059245 single base substitution C T synonymous_variant L829L 2487G>A BRCA-US 4 146059245 146059245 single base substitution C T synonymous_variant L894L 2682G>A BRCA-US 4 146059276 146059276 single base substitution G A intron_variant BRCA-US 4 146059276 146059276 single base substitution G A missense_variant S819F 2456C>T BRCA-US 4 146059276 146059276 single base substitution G A missense_variant S884F 2651C>T BRCA-US 4 146059425 146059425 single base substitution C A intron_variant BRCA-US 4 146059425 146059425 single base substitution C A missense_variant K769N 2307G>T BRCA-US 4 146059425 146059425 single base substitution C A missense_variant K834N 2502G>T BRCA-US 4 146062555 146062555 single base substitution G A downstream_gene_variant BRCA-US 4 146062555 146062555 single base substitution G A exon_variant BRCA-US 4 146062555 146062555 single base substitution G A stop_gained Q622* 1864C>T BRCA-US 4 146062555 146062555 single base substitution G A stop_gained Q687* 2059C>T BRCA-US 4 146067547 146067547 single base substitution G A exon_variant BRCA-US 4 146067547 146067547 single base substitution G A missense_variant H366Y 1096C>T BRCA-US 4 146067547 146067547 single base substitution G A missense_variant H367Y 1099C>T BRCA-US 4 146067547 146067547 single base substitution G A missense_variant H432Y 1294C>T BRCA-US 4 146076763 146076763 single base substitution A G downstream_gene_variant BRCA-US 4 146076763 146076763 single base substitution A G exon_variant BRCA-US 4 146076763 146076763 single base substitution A G missense_variant Y190H 568T>C BRCA-US 4 146076763 146076763 single base substitution A G missense_variant Y191H 571T>C BRCA-US 4 146076763 146076763 single base substitution A G missense_variant Y256H 766T>C BRCA-US 4 146076763 146076763 single base substitution A G upstream_gene_variant BRCA-US 4 146076764 146076764 single base substitution G C downstream_gene_variant BRCA-US 4 146076764 146076764 single base substitution G C exon_variant BRCA-US 4 146076764 146076764 single base substitution G C synonymous_variant V189V 567C>G BRCA-US 4 146076764 146076764 single base substitution G C synonymous_variant V190V 570C>G BRCA-US 4 146076764 146076764 single base substitution G C synonymous_variant V255V 765C>G BRCA-US 4 146076764 146076764 single base substitution G C upstream_gene_variant BRCA-US 4 146095895 146095895 single base substitution A G missense_variant V54A 161T>C BRCA-US 4 146095895 146095895 single base substitution A G splice_region_variant BRCA-US 4 146095895 146095895 single base substitution A G upstream_gene_variant BTCA-JP 4 146044682 146044682 single base substitution A G intron_variant BTCA-JP 4 146046124 146046124 deletion of <=200bp T - intron_variant BTCA-JP 4 146059244 146059244 single base substitution C T intron_variant BTCA-JP 4 146059244 146059244 single base substitution C T missense_variant E830K 2488G>A BTCA-JP 4 146059244 146059244 single base substitution C T missense_variant E895K 2683G>A BTCA-JP 4 146062585 146062585 single base substitution G T downstream_gene_variant BTCA-JP 4 146062585 146062585 single base substitution G T exon_variant BTCA-JP 4 146062585 146062585 single base substitution G T synonymous_variant R612R 1834C>A BTCA-JP 4 146062585 146062585 single base substitution G T synonymous_variant R677R 2029C>A BTCA-JP 4 146063434 146063434 single base substitution G T downstream_gene_variant BTCA-JP 4 146063434 146063434 single base substitution G T exon_variant BTCA-JP 4 146063434 146063434 single base substitution G T missense_variant P514Q 1541C>A BTCA-JP 4 146063434 146063434 single base substitution G T missense_variant P579Q 1736C>A BTCA-JP 4 146064657 146064657 single base substitution G A downstream_gene_variant BTCA-JP 4 146064657 146064657 single base substitution G A intron_variant BTCA-JP 4 146071751 146071751 single base substitution C T exon_variant BTCA-JP 4 146071751 146071751 single base substitution C T synonymous_variant A325A 975G>A BTCA-JP 4 146071751 146071751 single base substitution C T synonymous_variant A326A 978G>A BTCA-JP 4 146071751 146071751 single base substitution C T synonymous_variant A391A 1173G>A BTCA-JP 4 146073815 146073815 deletion of <=200bp A - downstream_gene_variant BTCA-JP 4 146073815 146073815 deletion of <=200bp A - intron_variant BTCA-JP 4 146073815 146073815 deletion of <=200bp A - upstream_gene_variant BTCA-JP 4 146073850 146073850 single base substitution C T downstream_gene_variant BTCA-JP 4 146073850 146073850 single base substitution C T intron_variant BTCA-JP 4 146073850 146073850 single base substitution C T upstream_gene_variant BTCA-JP 4 146077077 146077077 deletion of <=200bp A - downstream_gene_variant BTCA-JP 4 146077077 146077077 deletion of <=200bp A - intron_variant BTCA-JP 4 146080794 146080794 single base substitution T A intron_variant BTCA-JP 4 146080794 146080794 single base substitution T A splice_region_variant CESC-US 4 146044714 146044714 single base substitution T G intron_variant CESC-US 4 146058813 146058813 single base substitution T A intron_variant CESC-US 4 146058813 146058813 single base substitution T A missense_variant R1038S 3114A>T CESC-US 4 146058813 146058813 single base substitution T A missense_variant R973S 2919A>T CESC-US 4 146059410 146059410 single base substitution C T intron_variant CESC-US 4 146059410 146059410 single base substitution C T synonymous_variant Q774Q 2322G>A CESC-US 4 146059410 146059410 single base substitution C T synonymous_variant Q839Q 2517G>A CESC-US 4 146065559 146065559 single base substitution G A downstream_gene_variant CESC-US 4 146065559 146065559 single base substitution G A exon_variant CESC-US 4 146065559 146065559 single base substitution G A stop_gained Q419* 1255C>T CESC-US 4 146065559 146065559 single base substitution G A stop_gained Q484* 1450C>T CESC-US 4 146065567 146065567 single base substitution G A downstream_gene_variant CESC-US 4 146065567 146065567 single base substitution G A exon_variant CESC-US 4 146065567 146065567 single base substitution G A missense_variant S416L 1247C>T CESC-US 4 146065567 146065567 single base substitution G A missense_variant S481L 1442C>T CLLE-ES 4 146033985 146033985 insertion of <=200bp - TA intron_variant CLLE-ES 4 146038564 146038564 single base substitution A T intron_variant CLLE-ES 4 146057794 146057794 single base substitution T C 3_prime_UTR_variant CLLE-ES 4 146057794 146057794 single base substitution T C downstream_gene_variant CLLE-ES 4 146057794 146057794 single base substitution T C intron_variant CLLE-ES 4 146058801 146058801 single base substitution G T intron_variant CLLE-ES 4 146058801 146058801 single base substitution G T missense_variant F1042L 3126C>A CLLE-ES 4 146058801 146058801 single base substitution G T missense_variant F977L 2931C>A CLLE-ES 4 146063146 146063146 single base substitution G A downstream_gene_variant CLLE-ES 4 146063146 146063146 single base substitution G A intron_variant CLLE-ES 4 146097808 146097808 single base substitution G C intron_variant CLLE-ES 4 146097808 146097808 single base substitution G C upstream_gene_variant CLLE-ES 4 146102105 146102105 single base substitution C T upstream_gene_variant COAD-US 4 146030289 146030289 single base substitution C T downstream_gene_variant COAD-US 4 146030343 146030343 single base substitution A T downstream_gene_variant COAD-US 4 146031382 146031382 single base substitution A G downstream_gene_variant COAD-US 4 146041176 146041178 deletion of <=200bp GAA - intron_variant COAD-US 4 146041199 146041199 single base substitution T C intron_variant COAD-US 4 146044182 146044182 single base substitution C T intron_variant COAD-US 4 146058598 146058598 single base substitution C A intron_variant COAD-US 4 146058598 146058598 single base substitution C A missense_variant R1045M 3134G>T COAD-US 4 146058598 146058598 single base substitution C A missense_variant R1110M 3329G>T COAD-US 4 146058661 146058661 single base substitution C T intron_variant COAD-US 4 146058661 146058661 single base substitution C T missense_variant R1024Q 3071G>A COAD-US 4 146058661 146058661 single base substitution C T missense_variant R1089Q 3266G>A COAD-US 4 146059018 146059018 single base substitution C G intron_variant COAD-US 4 146059018 146059018 single base substitution C G missense_variant R905T 2714G>C COAD-US 4 146059018 146059018 single base substitution C G missense_variant R970T 2909G>C COAD-US 4 146059158 146059158 single base substitution G A intron_variant COAD-US 4 146059158 146059158 single base substitution G A synonymous_variant L858L 2574C>T COAD-US 4 146059158 146059158 single base substitution G A synonymous_variant L923L 2769C>T COAD-US 4 146061117 146061117 single base substitution T G exon_variant COAD-US 4 146061117 146061117 single base substitution T G missense_variant N639H 1915A>C COAD-US 4 146061117 146061117 single base substitution T G missense_variant N704H 2110A>C COAD-US 4 146067436 146067436 single base substitution C T downstream_gene_variant COAD-US 4 146067436 146067436 single base substitution C T exon_variant COAD-US 4 146067436 146067436 single base substitution C T missense_variant A404T 1210G>A COAD-US 4 146067436 146067436 single base substitution C T missense_variant A469T 1405G>A COAD-US 4 146076751 146076751 single base substitution C A downstream_gene_variant COAD-US 4 146076751 146076751 single base substitution C A exon_variant COAD-US 4 146076751 146076751 single base substitution C A stop_gained E194* 580G>T COAD-US 4 146076751 146076751 single base substitution C A stop_gained E195* 583G>T COAD-US 4 146076751 146076751 single base substitution C A stop_gained E260* 778G>T COAD-US 4 146076751 146076751 single base substitution C A upstream_gene_variant COCA-CN 4 146029187 146029187 single base substitution A T downstream_gene_variant COCA-CN 4 146030267 146030267 single base substitution T G downstream_gene_variant COCA-CN 4 146037793 146037793 single base substitution G A intron_variant COCA-CN 4 146040994 146040994 single base substitution T G intron_variant COCA-CN 4 146041413 146041413 single base substitution G A intron_variant COCA-CN 4 146058570 146058570 single base substitution C T 3_prime_UTR_variant COCA-CN 4 146058570 146058570 single base substitution C T intron_variant COCA-CN 4 146059682 146059682 single base substitution A G intron_variant COCA-CN 4 146059682 146059682 single base substitution A G missense_variant F684L 2050T>C COCA-CN 4 146059682 146059682 single base substitution A G missense_variant F749L 2245T>C COCA-CN 4 146059891 146059891 single base substitution A G intron_variant COCA-CN 4 146064440 146064440 single base substitution T C downstream_gene_variant COCA-CN 4 146064440 146064440 single base substitution T C intron_variant COCA-CN 4 146064568 146064568 single base substitution A C downstream_gene_variant COCA-CN 4 146064568 146064568 single base substitution A C exon_variant COCA-CN 4 146064568 146064568 single base substitution A C synonymous_variant V479V 1437T>G COCA-CN 4 146064568 146064568 single base substitution A C synonymous_variant V544V 1632T>G COCA-CN 4 146064598 146064598 single base substitution C A downstream_gene_variant COCA-CN 4 146064598 146064598 single base substitution C A splice_acceptor_variant COCA-CN 4 146065475 146065475 single base substitution G A downstream_gene_variant COCA-CN 4 146065475 146065475 single base substitution G A exon_variant COCA-CN 4 146065475 146065475 single base substitution G A stop_gained R447* 1339C>T COCA-CN 4 146065475 146065475 single base substitution G A stop_gained R512* 1534C>T COCA-CN 4 146065528 146065528 single base substitution G T downstream_gene_variant COCA-CN 4 146065528 146065528 single base substitution G T exon_variant COCA-CN 4 146065528 146065528 single base substitution G T stop_gained S429* 1286C>A COCA-CN 4 146065528 146065528 single base substitution G T stop_gained S494* 1481C>A COCA-CN 4 146067617 146067617 single base substitution A C intron_variant COCA-CN 4 146072149 146072149 single base substitution T G downstream_gene_variant COCA-CN 4 146072149 146072149 single base substitution T G intron_variant COCA-CN 4 146072149 146072149 single base substitution T G upstream_gene_variant COCA-CN 4 146076693 146076693 single base substitution T C downstream_gene_variant COCA-CN 4 146076693 146076693 single base substitution T C intron_variant COCA-CN 4 146076693 146076693 single base substitution T C upstream_gene_variant COCA-CN 4 146095825 146095825 single base substitution C A exon_variant COCA-CN 4 146095825 146095825 single base substitution C A missense_variant E12D 36G>T COCA-CN 4 146095825 146095825 single base substitution C A missense_variant E77D 231G>T COCA-CN 4 146095825 146095825 single base substitution C A upstream_gene_variant EOPC-DE 4 146096853 146096853 single base substitution C T intron_variant EOPC-DE 4 146096853 146096853 single base substitution C T upstream_gene_variant ESAD-UK 4 146029780 146029780 single base substitution A G downstream_gene_variant ESAD-UK 4 146035768 146035768 single base substitution T A intron_variant ESAD-UK 4 146035944 146035944 single base substitution A C intron_variant ESAD-UK 4 146040042 146040042 deletion of <=200bp T - intron_variant ESAD-UK 4 146040876 146040876 single base substitution G A intron_variant ESAD-UK 4 146044306 146044306 single base substitution A G intron_variant ESAD-UK 4 146047753 146047753 single base substitution C T intron_variant ESAD-UK 4 146049376 146049376 single base substitution C A intron_variant ESAD-UK 4 146051657 146051657 single base substitution T C downstream_gene_variant ESAD-UK 4 146051657 146051657 single base substitution T C intron_variant ESAD-UK 4 146055365 146055365 single base substitution G C 3_prime_UTR_variant ESAD-UK 4 146055365 146055365 single base substitution G C downstream_gene_variant ESAD-UK 4 146055365 146055365 single base substitution G C intron_variant ESAD-UK 4 146056195 146056195 single base substitution A G 3_prime_UTR_variant ESAD-UK 4 146056195 146056195 single base substitution A G downstream_gene_variant ESAD-UK 4 146056195 146056195 single base substitution A G intron_variant ESAD-UK 4 146059162 146059162 single base substitution G A intron_variant ESAD-UK 4 146059162 146059162 single base substitution G A missense_variant S857F 2570C>T ESAD-UK 4 146059162 146059162 single base substitution G A missense_variant S922F 2765C>T ESAD-UK 4 146060368 146060368 single base substitution A T intron_variant ESAD-UK 4 146063062 146063062 single base substitution C A downstream_gene_variant ESAD-UK 4 146063062 146063062 single base substitution C A intron_variant ESAD-UK 4 146066319 146066319 single base substitution T G downstream_gene_variant ESAD-UK 4 146066319 146066319 single base substitution T G intron_variant ESAD-UK 4 146068334 146068334 deletion of <=200bp A - intron_variant ESAD-UK 4 146070848 146070848 single base substitution A C intron_variant ESAD-UK 4 146071894 146071894 deletion of <=200bp A - intron_variant ESAD-UK 4 146072198 146072198 single base substitution T A downstream_gene_variant ESAD-UK 4 146072198 146072198 single base substitution T A intron_variant ESAD-UK 4 146072198 146072198 single base substitution T A upstream_gene_variant ESAD-UK 4 146074322 146074322 single base substitution C T downstream_gene_variant ESAD-UK 4 146074322 146074322 single base substitution C T intron_variant ESAD-UK 4 146074322 146074322 single base substitution C T upstream_gene_variant ESAD-UK 4 146075748 146075748 single base substitution C A downstream_gene_variant ESAD-UK 4 146075748 146075748 single base substitution C A intron_variant ESAD-UK 4 146075748 146075748 single base substitution C A upstream_gene_variant ESAD-UK 4 146077166 146077166 single base substitution C A downstream_gene_variant ESAD-UK 4 146077166 146077166 single base substitution C A intron_variant ESAD-UK 4 146078762 146078762 single base substitution C T downstream_gene_variant ESAD-UK 4 146078762 146078762 single base substitution C T intron_variant ESAD-UK 4 146079649 146079649 single base substitution C A downstream_gene_variant ESAD-UK 4 146079649 146079649 single base substitution C A intron_variant ESAD-UK 4 146088882 146088882 single base substitution T C downstream_gene_variant ESAD-UK 4 146088882 146088882 single base substitution T C intron_variant ESAD-UK 4 146093202 146093202 single base substitution G A intron_variant ESAD-UK 4 146093202 146093202 single base substitution G A upstream_gene_variant ESAD-UK 4 146094811 146094811 single base substitution G C intron_variant ESAD-UK 4 146094811 146094811 single base substitution G C upstream_gene_variant ESAD-UK 4 146098634 146098634 single base substitution T C intron_variant ESAD-UK 4 146100330 146100330 single base substitution A T intron_variant ESAD-UK 4 146100330 146100330 single base substitution A T upstream_gene_variant ESAD-UK 4 146102380 146102380 single base substitution T C upstream_gene_variant ESAD-UK 4 146104574 146104574 single base substitution C T upstream_gene_variant ESAD-UK 4 146106047 146106047 deletion of <=200bp C - upstream_gene_variant ESCA-CN 4 146056235 146056235 insertion of <=200bp - A 3_prime_UTR_variant ESCA-CN 4 146056235 146056235 insertion of <=200bp - A downstream_gene_variant ESCA-CN 4 146056235 146056235 insertion of <=200bp - A intron_variant ESCA-CN 4 146057606 146057606 single base substitution C G 3_prime_UTR_variant ESCA-CN 4 146057606 146057606 single base substitution C G downstream_gene_variant ESCA-CN 4 146057606 146057606 single base substitution C G intron_variant ESCA-CN 4 146059445 146059445 single base substitution C T intron_variant ESCA-CN 4 146059445 146059445 single base substitution C T missense_variant E763K 2287G>A ESCA-CN 4 146059445 146059445 single base substitution C T missense_variant E828K 2482G>A ESCA-CN 4 146100937 146100937 single base substitution T C intron_variant ESCA-CN 4 146100937 146100937 single base substitution T C upstream_gene_variant ESCA-CN 4 146100946 146100946 single base substitution T C intron_variant ESCA-CN 4 146100946 146100946 single base substitution T C upstream_gene_variant GBM-US 4 146059041 146059041 single base substitution A G intron_variant GBM-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C GBM-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C GBM-US 4 146059760 146059760 single base substitution G A intron_variant GBM-US 4 146059760 146059760 single base substitution G A missense_variant P658S 1972C>T GBM-US 4 146059760 146059760 single base substitution G A missense_variant P723S 2167C>T GBM-US 4 146077118 146077118 single base substitution C T downstream_gene_variant GBM-US 4 146077118 146077118 single base substitution C T exon_variant GBM-US 4 146077118 146077118 single base substitution C T synonymous_variant V155V 465G>A GBM-US 4 146077118 146077118 single base substitution C T synonymous_variant V220V 660G>A KIRC-US 4 146041212 146041212 single base substitution C A intron_variant KIRC-US 4 146063397 146063397 insertion of <=200bp - G downstream_gene_variant KIRC-US 4 146063397 146063397 insertion of <=200bp - G exon_variant KIRC-US 4 146063397 146063397 insertion of <=200bp - G frameshift_variant P526P? KIRC-US 4 146063397 146063397 insertion of <=200bp - G frameshift_variant P591P? KIRC-US 4 146063450 146063450 single base substitution G A downstream_gene_variant KIRC-US 4 146063450 146063450 single base substitution G A exon_variant KIRC-US 4 146063450 146063450 single base substitution G A missense_variant P509S 1525C>T KIRC-US 4 146063450 146063450 single base substitution G A missense_variant P574S 1720C>T KIRC-US 4 146076739 146076739 deletion of <=200bp A - downstream_gene_variant KIRC-US 4 146076739 146076739 deletion of <=200bp A - exon_variant KIRC-US 4 146076739 146076739 deletion of <=200bp A - frameshift_variant W198 KIRC-US 4 146076739 146076739 deletion of <=200bp A - frameshift_variant W199 KIRC-US 4 146076739 146076739 deletion of <=200bp A - frameshift_variant W264 KIRC-US 4 146076739 146076739 deletion of <=200bp A - upstream_gene_variant KIRP-US 4 146076795 146076795 single base substitution C A downstream_gene_variant KIRP-US 4 146076795 146076795 single base substitution C A exon_variant KIRP-US 4 146076795 146076795 single base substitution C A missense_variant R179I 536G>T KIRP-US 4 146076795 146076795 single base substitution C A missense_variant R180I 539G>T KIRP-US 4 146076795 146076795 single base substitution C A missense_variant R245I 734G>T KIRP-US 4 146076795 146076795 single base substitution C A upstream_gene_variant LAML-KR 4 146089581 146089581 single base substitution G A downstream_gene_variant LAML-KR 4 146089581 146089581 single base substitution G A intron_variant LGG-US 4 146044497 146044497 single base substitution G A intron_variant LGG-US 4 146058891 146058891 single base substitution A C intron_variant LGG-US 4 146058891 146058891 single base substitution A C synonymous_variant V1012V 3036T>G LGG-US 4 146058891 146058891 single base substitution A C synonymous_variant V947V 2841T>G LGG-US 4 146059006 146059006 single base substitution G A intron_variant LGG-US 4 146059006 146059006 single base substitution G A missense_variant T909I 2726C>T LGG-US 4 146059006 146059006 single base substitution G A missense_variant T974I 2921C>T LGG-US 4 146059041 146059041 single base substitution A G intron_variant LGG-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C LGG-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C LGG-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD153D LGG-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD218D LGG-US 4 146077123 146077125 deletion of <=200bp CAG - downstream_gene_variant LGG-US 4 146077123 146077125 deletion of <=200bp CAG - exon_variant LICA-CN 4 146058647 146058647 single base substitution G A intron_variant LICA-CN 4 146058647 146058647 single base substitution G A stop_gained R1029* 3085C>T LICA-CN 4 146058647 146058647 single base substitution G A stop_gained R1094* 3280C>T LICA-FR 4 146027206 146027206 single base substitution A G downstream_gene_variant LICA-FR 4 146039058 146039058 single base substitution A G intron_variant LICA-FR 4 146041307 146041307 insertion of <=200bp - T intron_variant LICA-FR 4 146058974 146058974 single base substitution T C intron_variant LICA-FR 4 146058974 146058974 single base substitution T C missense_variant I920V 2758A>G LICA-FR 4 146058974 146058974 single base substitution T C missense_variant I985V 2953A>G LICA-FR 4 146062744 146062744 single base substitution T C downstream_gene_variant LICA-FR 4 146062744 146062744 single base substitution T C exon_variant LICA-FR 4 146062744 146062744 single base substitution T C missense_variant T559A 1675A>G LICA-FR 4 146062744 146062744 single base substitution T C missense_variant T624A 1870A>G LICA-FR 4 146071812 146071812 single base substitution A G exon_variant LICA-FR 4 146071812 146071812 single base substitution A G missense_variant I305T 914T>C LICA-FR 4 146071812 146071812 single base substitution A G missense_variant I306T 917T>C LICA-FR 4 146071812 146071812 single base substitution A G missense_variant I371T 1112T>C LICA-FR 4 146095159 146095159 deletion of <=200bp T - intron_variant LICA-FR 4 146095159 146095159 deletion of <=200bp T - upstream_gene_variant LICA-FR 4 146097686 146097686 deletion of <=200bp A - intron_variant LICA-FR 4 146097686 146097686 deletion of <=200bp A - upstream_gene_variant LIHC-US 4 146029198 146029198 single base substitution A G downstream_gene_variant LINC-JP 4 146032454 146032454 single base substitution A G intron_variant LINC-JP 4 146037743 146037743 single base substitution A G intron_variant LINC-JP 4 146042013 146042013 single base substitution T C intron_variant LINC-JP 4 146045116 146045116 single base substitution G T intron_variant LINC-JP 4 146048234 146048234 single base substitution A C intron_variant LINC-JP 4 146049738 146049738 single base substitution T C intron_variant LINC-JP 4 146059837 146059837 single base substitution A T intron_variant LINC-JP 4 146061850 146061850 single base substitution C T intron_variant LINC-JP 4 146061926 146061926 single base substitution T C intron_variant LINC-JP 4 146071990 146071991 deletion of <=200bp TC - downstream_gene_variant LINC-JP 4 146071990 146071991 deletion of <=200bp TC - exon_variant LINC-JP 4 146071990 146071991 deletion of <=200bp TC - frameshift_variant MK279 LINC-JP 4 146071990 146071991 deletion of <=200bp TC - frameshift_variant MK280 LINC-JP 4 146071990 146071991 deletion of <=200bp TC - frameshift_variant MK345 LINC-JP 4 146072095 146072095 single base substitution C A downstream_gene_variant LINC-JP 4 146072095 146072095 single base substitution C A intron_variant LINC-JP 4 146072095 146072095 single base substitution C A upstream_gene_variant LINC-JP 4 146078870 146078870 single base substitution T C downstream_gene_variant LINC-JP 4 146078870 146078870 single base substitution T C intron_variant LINC-JP 4 146084430 146084430 single base substitution C G intron_variant LINC-JP 4 146085890 146085890 single base substitution T C intron_variant LIRI-JP 4 146027123 146027123 single base substitution C G downstream_gene_variant LIRI-JP 4 146027670 146027670 single base substitution T A downstream_gene_variant LIRI-JP 4 146027671 146027671 single base substitution A T downstream_gene_variant LIRI-JP 4 146027812 146027812 single base substitution A C downstream_gene_variant LIRI-JP 4 146028495 146028495 single base substitution G A downstream_gene_variant LIRI-JP 4 146029659 146029659 single base substitution A G downstream_gene_variant LIRI-JP 4 146030938 146030938 single base substitution T C downstream_gene_variant LIRI-JP 4 146031571 146031571 single base substitution A T downstream_gene_variant LIRI-JP 4 146031652 146031652 single base substitution A C downstream_gene_variant LIRI-JP 4 146035497 146035497 single base substitution T C intron_variant LIRI-JP 4 146038186 146038186 single base substitution C T intron_variant LIRI-JP 4 146040254 146040254 single base substitution T C intron_variant LIRI-JP 4 146042192 146042192 single base substitution A G intron_variant LIRI-JP 4 146042298 146042298 single base substitution A G intron_variant LIRI-JP 4 146043182 146043182 single base substitution G T intron_variant LIRI-JP 4 146045672 146045672 single base substitution C A intron_variant LIRI-JP 4 146046634 146046634 single base substitution A T intron_variant LIRI-JP 4 146047730 146047730 single base substitution A C intron_variant LIRI-JP 4 146048946 146048946 single base substitution T C intron_variant LIRI-JP 4 146051420 146051420 single base substitution A G downstream_gene_variant LIRI-JP 4 146051420 146051420 single base substitution A G intron_variant LIRI-JP 4 146051600 146051600 single base substitution A G downstream_gene_variant LIRI-JP 4 146051600 146051600 single base substitution A G intron_variant LIRI-JP 4 146052472 146052472 single base substitution A G downstream_gene_variant LIRI-JP 4 146052472 146052472 single base substitution A G intron_variant LIRI-JP 4 146056036 146056038 deletion of <=200bp TGG - 3_prime_UTR_variant LIRI-JP 4 146056036 146056038 deletion of <=200bp TGG - downstream_gene_variant LIRI-JP 4 146056036 146056038 deletion of <=200bp TGG - intron_variant LIRI-JP 4 146057288 146057288 single base substitution T G 3_prime_UTR_variant LIRI-JP 4 146057288 146057288 single base substitution T G downstream_gene_variant LIRI-JP 4 146057288 146057288 single base substitution T G intron_variant LIRI-JP 4 146057349 146057349 single base substitution T C 3_prime_UTR_variant LIRI-JP 4 146057349 146057349 single base substitution T C downstream_gene_variant LIRI-JP 4 146057349 146057349 single base substitution T C intron_variant LIRI-JP 4 146059827 146059827 single base substitution T C intron_variant LIRI-JP 4 146059927 146059927 single base substitution T C intron_variant LIRI-JP 4 146060030 146060030 deletion of <=200bp G - intron_variant LIRI-JP 4 146060807 146060807 single base substitution T A intron_variant LIRI-JP 4 146060986 146060988 deletion of <=200bp ATG - intron_variant LIRI-JP 4 146065343 146065343 single base substitution T C downstream_gene_variant LIRI-JP 4 146065343 146065343 single base substitution T C intron_variant LIRI-JP 4 146067858 146067858 single base substitution G A intron_variant LIRI-JP 4 146067984 146067984 single base substitution T C intron_variant LIRI-JP 4 146071554 146071554 single base substitution G A intron_variant LIRI-JP 4 146073671 146073671 single base substitution T C downstream_gene_variant LIRI-JP 4 146073671 146073671 single base substitution T C intron_variant LIRI-JP 4 146073671 146073671 single base substitution T C upstream_gene_variant LIRI-JP 4 146077123 146077123 insertion of <=200bp - CAG downstream_gene_variant LIRI-JP 4 146077123 146077123 insertion of <=200bp - CAG exon_variant LIRI-JP 4 146077123 146077123 insertion of <=200bp - CAG inframe_insertion D154AD LIRI-JP 4 146077123 146077123 insertion of <=200bp - CAG inframe_insertion D219AD LIRI-JP 4 146077427 146077427 single base substitution T C downstream_gene_variant LIRI-JP 4 146077427 146077427 single base substitution T C intron_variant LIRI-JP 4 146078603 146078603 single base substitution G T downstream_gene_variant LIRI-JP 4 146078603 146078603 single base substitution G T intron_variant LIRI-JP 4 146079273 146079273 single base substitution A G downstream_gene_variant LIRI-JP 4 146079273 146079273 single base substitution A G intron_variant LIRI-JP 4 146079443 146079443 single base substitution G A downstream_gene_variant LIRI-JP 4 146079443 146079443 single base substitution G A intron_variant LIRI-JP 4 146081510 146081510 insertion of <=200bp - A intron_variant LIRI-JP 4 146086409 146086409 single base substitution T C intron_variant LIRI-JP 4 146088944 146088944 single base substitution A T downstream_gene_variant LIRI-JP 4 146088944 146088944 single base substitution A T intron_variant LIRI-JP 4 146089413 146089413 single base substitution T C downstream_gene_variant LIRI-JP 4 146089413 146089413 single base substitution T C intron_variant LIRI-JP 4 146089741 146089741 single base substitution T C downstream_gene_variant LIRI-JP 4 146089741 146089741 single base substitution T C intron_variant LIRI-JP 4 146091213 146091213 single base substitution T A downstream_gene_variant LIRI-JP 4 146091213 146091213 single base substitution T A intron_variant LIRI-JP 4 146092383 146092383 single base substitution A T exon_variant LIRI-JP 4 146092383 146092383 single base substitution A T intron_variant LIRI-JP 4 146093978 146093978 single base substitution T C intron_variant LIRI-JP 4 146093978 146093978 single base substitution T C upstream_gene_variant LIRI-JP 4 146095310 146095310 single base substitution A G intron_variant LIRI-JP 4 146095310 146095310 single base substitution A G upstream_gene_variant LIRI-JP 4 146095363 146095363 single base substitution T G intron_variant LIRI-JP 4 146095363 146095363 single base substitution T G upstream_gene_variant LIRI-JP 4 146095901 146095901 single base substitution A C splice_region_variant LIRI-JP 4 146095901 146095901 single base substitution A C upstream_gene_variant LIRI-JP 4 146097421 146097421 single base substitution T C intron_variant LIRI-JP 4 146097421 146097421 single base substitution T C upstream_gene_variant LIRI-JP 4 146099344 146099344 single base substitution T C intron_variant LIRI-JP 4 146099344 146099344 single base substitution T C upstream_gene_variant LIRI-JP 4 146102451 146102451 single base substitution T C upstream_gene_variant LIRI-JP 4 146102635 146102635 single base substitution C A upstream_gene_variant LIRI-JP 4 146102812 146102812 single base substitution T A upstream_gene_variant LIRI-JP 4 146103378 146103378 single base substitution T A upstream_gene_variant LIRI-JP 4 146103644 146103644 single base substitution A G upstream_gene_variant LIRI-JP 4 146105630 146105630 single base substitution G T upstream_gene_variant LUSC-KR 4 146028460 146028460 single base substitution A G downstream_gene_variant LUSC-KR 4 146033837 146033837 single base substitution G C intron_variant LUSC-KR 4 146038321 146038321 single base substitution T C intron_variant LUSC-KR 4 146039837 146039837 single base substitution A G intron_variant LUSC-KR 4 146044171 146044171 single base substitution A T intron_variant LUSC-KR 4 146055367 146055367 single base substitution G C 3_prime_UTR_variant LUSC-KR 4 146055367 146055367 single base substitution G C downstream_gene_variant LUSC-KR 4 146055367 146055367 single base substitution G C intron_variant LUSC-KR 4 146067556 146067556 single base substitution C T exon_variant LUSC-KR 4 146067556 146067556 single base substitution C T missense_variant D363N 1087G>A LUSC-KR 4 146067556 146067556 single base substitution C T missense_variant D364N 1090G>A LUSC-KR 4 146067556 146067556 single base substitution C T missense_variant D429N 1285G>A LUSC-KR 4 146067635 146067635 single base substitution T A intron_variant LUSC-KR 4 146067639 146067639 single base substitution T A intron_variant LUSC-KR 4 146076385 146076385 single base substitution G A downstream_gene_variant LUSC-KR 4 146076385 146076385 single base substitution G A intron_variant LUSC-KR 4 146076385 146076385 single base substitution G A upstream_gene_variant LUSC-KR 4 146076565 146076565 single base substitution G C downstream_gene_variant LUSC-KR 4 146076565 146076565 single base substitution G C missense_variant Q225E 673C>G LUSC-KR 4 146076565 146076565 single base substitution G C missense_variant Q226E 676C>G LUSC-KR 4 146076565 146076565 single base substitution G C missense_variant Q291E 871C>G LUSC-KR 4 146076565 146076565 single base substitution G C splice_region_variant LUSC-KR 4 146076565 146076565 single base substitution G C upstream_gene_variant LUSC-KR 4 146076649 146076649 single base substitution G C downstream_gene_variant LUSC-KR 4 146076649 146076649 single base substitution G C intron_variant LUSC-KR 4 146076649 146076649 single base substitution G C upstream_gene_variant LUSC-KR 4 146077373 146077373 single base substitution G A downstream_gene_variant LUSC-KR 4 146077373 146077373 single base substitution G A intron_variant LUSC-KR 4 146077608 146077608 single base substitution G A downstream_gene_variant LUSC-KR 4 146077608 146077608 single base substitution G A intron_variant LUSC-KR 4 146078525 146078525 single base substitution T C downstream_gene_variant LUSC-KR 4 146078525 146078525 single base substitution T C intron_variant LUSC-KR 4 146081926 146081926 single base substitution C A intron_variant LUSC-KR 4 146083691 146083691 single base substitution G A intron_variant LUSC-KR 4 146087795 146087795 single base substitution C A downstream_gene_variant LUSC-KR 4 146087795 146087795 single base substitution C A intron_variant LUSC-KR 4 146089557 146089557 single base substitution T A downstream_gene_variant LUSC-KR 4 146089557 146089557 single base substitution T A intron_variant LUSC-KR 4 146101105 146101105 single base substitution G A synonymous_variant V7V 21C>T LUSC-KR 4 146101105 146101105 single base substitution G A upstream_gene_variant LUSC-KR 4 146101826 146101826 single base substitution G T upstream_gene_variant LUSC-KR 4 146101988 146101988 single base substitution G T upstream_gene_variant LUSC-KR 4 146102816 146102816 single base substitution T A upstream_gene_variant LUSC-KR 4 146103273 146103273 single base substitution G C upstream_gene_variant LUSC-KR 4 146103685 146103685 single base substitution C G upstream_gene_variant LUSC-US 4 146064527 146064527 single base substitution G A downstream_gene_variant LUSC-US 4 146064527 146064527 single base substitution G A exon_variant LUSC-US 4 146064527 146064527 single base substitution G A missense_variant P493L 1478C>T LUSC-US 4 146064527 146064527 single base substitution G A missense_variant P558L 1673C>T LUSC-US 4 146067571 146067571 single base substitution G C exon_variant LUSC-US 4 146067571 146067571 single base substitution G C missense_variant R358G 1072C>G LUSC-US 4 146067571 146067571 single base substitution G C missense_variant R359G 1075C>G LUSC-US 4 146067571 146067571 single base substitution G C missense_variant R424G 1270C>G LUSC-US 4 146073750 146073750 single base substitution T A downstream_gene_variant LUSC-US 4 146073750 146073750 single base substitution T A exon_variant LUSC-US 4 146073750 146073750 single base substitution T A missense_variant D238V 713A>T LUSC-US 4 146073750 146073750 single base substitution T A missense_variant D239V 716A>T LUSC-US 4 146073750 146073750 single base substitution T A missense_variant D304V 911A>T LUSC-US 4 146073750 146073750 single base substitution T A upstream_gene_variant LUSC-US 4 146080657 146080657 single base substitution G C downstream_gene_variant LUSC-US 4 146080657 146080657 single base substitution G C missense_variant C144W 432C>G LUSC-US 4 146080657 146080657 single base substitution G C missense_variant C209W 627C>G LUSC-US 4 146080657 146080657 single base substitution G C splice_region_variant MALY-DE 4 146032753 146032753 single base substitution A T intron_variant MALY-DE 4 146043461 146043461 deletion of <=200bp T - intron_variant MALY-DE 4 146057348 146057348 single base substitution A C 3_prime_UTR_variant MALY-DE 4 146057348 146057348 single base substitution A C downstream_gene_variant MALY-DE 4 146057348 146057348 single base substitution A C intron_variant MALY-DE 4 146058272 146058272 single base substitution C A 3_prime_UTR_variant MALY-DE 4 146058272 146058272 single base substitution C A downstream_gene_variant MALY-DE 4 146058272 146058272 single base substitution C A intron_variant MALY-DE 4 146068724 146068724 single base substitution A G intron_variant MALY-DE 4 146069702 146069702 single base substitution A C intron_variant MALY-DE 4 146077587 146077587 single base substitution G C downstream_gene_variant MALY-DE 4 146077587 146077587 single base substitution G C intron_variant MALY-DE 4 146082787 146082787 single base substitution T A intron_variant MALY-DE 4 146085903 146085903 insertion of <=200bp - A intron_variant MALY-DE 4 146088838 146088838 single base substitution A G downstream_gene_variant MALY-DE 4 146088838 146088838 single base substitution A G intron_variant MALY-DE 4 146098578 146098578 single base substitution T C intron_variant MALY-DE 4 146099671 146099673 deletion of <=200bp AAC - 5_prime_UTR_variant MALY-DE 4 146099671 146099673 deletion of <=200bp AAC - intron_variant MALY-DE 4 146099671 146099673 deletion of <=200bp AAC - upstream_gene_variant MALY-DE 4 146100089 146100089 single base substitution T A intron_variant MALY-DE 4 146100089 146100089 single base substitution T A upstream_gene_variant MALY-DE 4 146100602 146100602 single base substitution G T intron_variant MALY-DE 4 146100602 146100602 single base substitution G T upstream_gene_variant MALY-DE 4 146100683 146100683 single base substitution A G intron_variant MALY-DE 4 146100683 146100683 single base substitution A G upstream_gene_variant MELA-AU 4 146027556 146027556 single base substitution C T downstream_gene_variant MELA-AU 4 146027862 146027862 single base substitution C T downstream_gene_variant MELA-AU 4 146028612 146028612 single base substitution C T downstream_gene_variant MELA-AU 4 146028799 146028799 single base substitution C T downstream_gene_variant MELA-AU 4 146030997 146030997 single base substitution C T downstream_gene_variant MELA-AU 4 146031085 146031086 multiple base substitution (>=2bp and <=200bp) CT TA downstream_gene_variant MELA-AU 4 146031117 146031117 single base substitution A G downstream_gene_variant MELA-AU 4 146031257 146031257 single base substitution T G downstream_gene_variant MELA-AU 4 146032215 146032215 single base substitution A G exon_variant MELA-AU 4 146032601 146032601 single base substitution G A intron_variant MELA-AU 4 146032969 146032969 single base substitution C T intron_variant MELA-AU 4 146035537 146035537 deletion of <=200bp G - intron_variant MELA-AU 4 146036093 146036093 single base substitution T G intron_variant MELA-AU 4 146036646 146036646 single base substitution C T intron_variant MELA-AU 4 146036652 146036652 single base substitution C T intron_variant MELA-AU 4 146037121 146037121 single base substitution A G intron_variant MELA-AU 4 146037828 146037828 single base substitution T C intron_variant MELA-AU 4 146037830 146037830 single base substitution C T intron_variant MELA-AU 4 146037926 146037926 single base substitution G A intron_variant MELA-AU 4 146037997 146037997 single base substitution C T intron_variant MELA-AU 4 146038518 146038518 single base substitution G C intron_variant MELA-AU 4 146038602 146038602 single base substitution C G intron_variant MELA-AU 4 146039044 146039044 single base substitution C T intron_variant MELA-AU 4 146039179 146039179 insertion of <=200bp - TACT intron_variant MELA-AU 4 146039264 146039264 single base substitution C T intron_variant MELA-AU 4 146042087 146042087 single base substitution C T intron_variant MELA-AU 4 146042539 146042539 single base substitution C T intron_variant MELA-AU 4 146042721 146042721 single base substitution C T intron_variant MELA-AU 4 146043864 146043864 single base substitution G A intron_variant MELA-AU 4 146045216 146045216 single base substitution C T intron_variant MELA-AU 4 146045234 146045234 single base substitution T A intron_variant MELA-AU 4 146045672 146045672 single base substitution C T intron_variant MELA-AU 4 146045766 146045766 single base substitution C T intron_variant MELA-AU 4 146045966 146045966 single base substitution C T intron_variant MELA-AU 4 146046118 146046118 single base substitution A G intron_variant MELA-AU 4 146046137 146046137 single base substitution C T intron_variant MELA-AU 4 146046157 146046158 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 146046553 146046553 single base substitution G A intron_variant MELA-AU 4 146046578 146046578 single base substitution C T intron_variant MELA-AU 4 146046668 146046668 single base substitution C T intron_variant MELA-AU 4 146047184 146047184 single base substitution C T intron_variant MELA-AU 4 146047190 146047190 insertion of <=200bp - CCCTGC intron_variant MELA-AU 4 146047430 146047430 deletion of <=200bp T - intron_variant MELA-AU 4 146047688 146047688 single base substitution C T intron_variant MELA-AU 4 146047899 146047899 single base substitution T A intron_variant MELA-AU 4 146049775 146049775 single base substitution C T intron_variant MELA-AU 4 146049996 146049996 single base substitution G A downstream_gene_variant MELA-AU 4 146049996 146049996 single base substitution G A intron_variant MELA-AU 4 146050799 146050799 deletion of <=200bp G - downstream_gene_variant MELA-AU 4 146050799 146050799 deletion of <=200bp G - intron_variant MELA-AU 4 146051100 146051100 single base substitution T C downstream_gene_variant MELA-AU 4 146051100 146051100 single base substitution T C intron_variant MELA-AU 4 146051131 146051131 single base substitution T A downstream_gene_variant MELA-AU 4 146051131 146051131 single base substitution T A intron_variant MELA-AU 4 146051747 146051747 single base substitution C T downstream_gene_variant MELA-AU 4 146051747 146051747 single base substitution C T intron_variant MELA-AU 4 146052719 146052719 single base substitution T G downstream_gene_variant MELA-AU 4 146052719 146052719 single base substitution T G intron_variant MELA-AU 4 146056006 146056006 single base substitution C T 3_prime_UTR_variant MELA-AU 4 146056006 146056006 single base substitution C T downstream_gene_variant MELA-AU 4 146056006 146056006 single base substitution C T intron_variant MELA-AU 4 146056222 146056222 single base substitution T G 3_prime_UTR_variant MELA-AU 4 146056222 146056222 single base substitution T G downstream_gene_variant MELA-AU 4 146056222 146056222 single base substitution T G intron_variant MELA-AU 4 146056496 146056496 single base substitution T C 3_prime_UTR_variant MELA-AU 4 146056496 146056496 single base substitution T C downstream_gene_variant MELA-AU 4 146056496 146056496 single base substitution T C intron_variant MELA-AU 4 146056810 146056810 single base substitution G C 3_prime_UTR_variant MELA-AU 4 146056810 146056810 single base substitution G C downstream_gene_variant MELA-AU 4 146056810 146056810 single base substitution G C intron_variant MELA-AU 4 146059123 146059123 deletion of <=200bp C - frameshift_variant G870 MELA-AU 4 146059123 146059123 deletion of <=200bp C - frameshift_variant G935 MELA-AU 4 146059123 146059123 deletion of <=200bp C - intron_variant MELA-AU 4 146059473 146059473 single base substitution G A intron_variant MELA-AU 4 146059473 146059473 single base substitution G A synonymous_variant T753T 2259C>T MELA-AU 4 146059473 146059473 single base substitution G A synonymous_variant T818T 2454C>T MELA-AU 4 146060602 146060603 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 146060932 146060932 single base substitution C G intron_variant MELA-AU 4 146061924 146061924 single base substitution T A intron_variant MELA-AU 4 146062828 146062828 single base substitution G A downstream_gene_variant MELA-AU 4 146062828 146062828 single base substitution G A intron_variant MELA-AU 4 146063557 146063557 single base substitution A G downstream_gene_variant MELA-AU 4 146063557 146063557 single base substitution A G intron_variant MELA-AU 4 146063981 146063981 single base substitution T A downstream_gene_variant MELA-AU 4 146063981 146063981 single base substitution T A intron_variant MELA-AU 4 146064209 146064209 single base substitution A G downstream_gene_variant MELA-AU 4 146064209 146064209 single base substitution A G intron_variant MELA-AU 4 146065814 146065814 single base substitution C T downstream_gene_variant MELA-AU 4 146065814 146065814 single base substitution C T intron_variant MELA-AU 4 146066459 146066459 single base substitution G A downstream_gene_variant MELA-AU 4 146066459 146066459 single base substitution G A intron_variant MELA-AU 4 146067115 146067115 single base substitution T C downstream_gene_variant MELA-AU 4 146067115 146067115 single base substitution T C intron_variant MELA-AU 4 146067952 146067952 single base substitution A G intron_variant MELA-AU 4 146068330 146068330 single base substitution C T intron_variant MELA-AU 4 146068521 146068521 single base substitution G A intron_variant MELA-AU 4 146069038 146069038 single base substitution T C intron_variant MELA-AU 4 146069363 146069363 single base substitution G A intron_variant MELA-AU 4 146069868 146069868 single base substitution G A intron_variant MELA-AU 4 146069902 146069902 single base substitution G A intron_variant MELA-AU 4 146069979 146069979 single base substitution C T intron_variant MELA-AU 4 146071346 146071346 single base substitution G A intron_variant MELA-AU 4 146071734 146071734 single base substitution G C exon_variant MELA-AU 4 146071734 146071734 single base substitution G C stop_gained S331* 992C>G MELA-AU 4 146071734 146071734 single base substitution G C stop_gained S332* 995C>G MELA-AU 4 146071734 146071734 single base substitution G C stop_gained S397* 1190C>G MELA-AU 4 146071983 146071983 single base substitution G A downstream_gene_variant MELA-AU 4 146071983 146071983 single base substitution G A exon_variant MELA-AU 4 146071983 146071983 single base substitution G A missense_variant P282L 845C>T MELA-AU 4 146071983 146071983 single base substitution G A missense_variant P283L 848C>T MELA-AU 4 146071983 146071983 single base substitution G A missense_variant P348L 1043C>T MELA-AU 4 146072688 146072688 single base substitution G A downstream_gene_variant MELA-AU 4 146072688 146072688 single base substitution G A intron_variant MELA-AU 4 146072688 146072688 single base substitution G A upstream_gene_variant MELA-AU 4 146072799 146072799 single base substitution A T downstream_gene_variant MELA-AU 4 146072799 146072799 single base substitution A T intron_variant MELA-AU 4 146072799 146072799 single base substitution A T upstream_gene_variant MELA-AU 4 146072884 146072884 single base substitution G A downstream_gene_variant MELA-AU 4 146072884 146072884 single base substitution G A intron_variant MELA-AU 4 146072884 146072884 single base substitution G A upstream_gene_variant MELA-AU 4 146074313 146074313 single base substitution A C downstream_gene_variant MELA-AU 4 146074313 146074313 single base substitution A C intron_variant MELA-AU 4 146074313 146074313 single base substitution A C upstream_gene_variant MELA-AU 4 146074330 146074330 single base substitution C T downstream_gene_variant MELA-AU 4 146074330 146074330 single base substitution C T intron_variant MELA-AU 4 146074330 146074330 single base substitution C T upstream_gene_variant MELA-AU 4 146074734 146074734 single base substitution C T downstream_gene_variant MELA-AU 4 146074734 146074734 single base substitution C T intron_variant MELA-AU 4 146074734 146074734 single base substitution C T upstream_gene_variant MELA-AU 4 146075597 146075597 single base substitution G A downstream_gene_variant MELA-AU 4 146075597 146075597 single base substitution G A intron_variant MELA-AU 4 146075597 146075597 single base substitution G A upstream_gene_variant MELA-AU 4 146076875 146076875 single base substitution G A downstream_gene_variant MELA-AU 4 146076875 146076875 single base substitution G A intron_variant MELA-AU 4 146076875 146076875 single base substitution G A upstream_gene_variant MELA-AU 4 146078744 146078744 single base substitution G A downstream_gene_variant MELA-AU 4 146078744 146078744 single base substitution G A intron_variant MELA-AU 4 146078791 146078791 single base substitution A C downstream_gene_variant MELA-AU 4 146078791 146078791 single base substitution A C intron_variant MELA-AU 4 146078844 146078844 single base substitution A T downstream_gene_variant MELA-AU 4 146078844 146078844 single base substitution A T intron_variant MELA-AU 4 146079275 146079275 single base substitution G A downstream_gene_variant MELA-AU 4 146079275 146079275 single base substitution G A intron_variant MELA-AU 4 146079315 146079315 single base substitution A T downstream_gene_variant MELA-AU 4 146079315 146079315 single base substitution A T intron_variant MELA-AU 4 146080294 146080294 single base substitution G A 3_prime_UTR_variant MELA-AU 4 146080294 146080294 single base substitution G A downstream_gene_variant MELA-AU 4 146080294 146080294 single base substitution G A intron_variant MELA-AU 4 146080631 146080631 single base substitution G A 3_prime_UTR_variant MELA-AU 4 146080631 146080631 single base substitution G A downstream_gene_variant MELA-AU 4 146080631 146080631 single base substitution G A intron_variant MELA-AU 4 146081709 146081709 single base substitution A C intron_variant MELA-AU 4 146081942 146081942 single base substitution G A intron_variant MELA-AU 4 146082154 146082154 single base substitution C G intron_variant MELA-AU 4 146082541 146082541 single base substitution G A intron_variant MELA-AU 4 146083070 146083070 single base substitution T G intron_variant MELA-AU 4 146083522 146083522 single base substitution G A intron_variant MELA-AU 4 146084349 146084349 single base substitution A C intron_variant MELA-AU 4 146084618 146084618 single base substitution G A intron_variant MELA-AU 4 146084805 146084805 single base substitution G A intron_variant MELA-AU 4 146084962 146084962 single base substitution G A intron_variant MELA-AU 4 146085129 146085129 single base substitution G A intron_variant MELA-AU 4 146086184 146086184 single base substitution G A intron_variant MELA-AU 4 146087759 146087759 single base substitution C T downstream_gene_variant MELA-AU 4 146087759 146087759 single base substitution C T intron_variant MELA-AU 4 146088667 146088667 single base substitution G A downstream_gene_variant MELA-AU 4 146088667 146088667 single base substitution G A intron_variant MELA-AU 4 146089844 146089844 single base substitution C T downstream_gene_variant MELA-AU 4 146089844 146089844 single base substitution C T intron_variant MELA-AU 4 146090126 146090126 single base substitution G A downstream_gene_variant MELA-AU 4 146090126 146090126 single base substitution G A intron_variant MELA-AU 4 146090190 146090190 single base substitution T C downstream_gene_variant MELA-AU 4 146090190 146090190 single base substitution T C intron_variant MELA-AU 4 146090318 146090318 single base substitution G A downstream_gene_variant MELA-AU 4 146090318 146090318 single base substitution G A intron_variant MELA-AU 4 146090893 146090894 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 146090893 146090894 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 146090927 146090927 single base substitution G A downstream_gene_variant MELA-AU 4 146090927 146090927 single base substitution G A intron_variant MELA-AU 4 146091012 146091013 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 4 146091012 146091013 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 146091395 146091395 single base substitution G A downstream_gene_variant MELA-AU 4 146091395 146091395 single base substitution G A intron_variant MELA-AU 4 146091481 146091481 single base substitution T G downstream_gene_variant MELA-AU 4 146091481 146091481 single base substitution T G intron_variant MELA-AU 4 146092187 146092188 multiple base substitution (>=2bp and <=200bp) AG GA exon_variant MELA-AU 4 146092187 146092188 multiple base substitution (>=2bp and <=200bp) AG GA intron_variant MELA-AU 4 146092268 146092268 single base substitution C G exon_variant MELA-AU 4 146092268 146092268 single base substitution C G intron_variant MELA-AU 4 146092793 146092793 single base substitution T A intron_variant MELA-AU 4 146093081 146093081 single base substitution G A intron_variant MELA-AU 4 146093081 146093081 single base substitution G A upstream_gene_variant MELA-AU 4 146093135 146093135 single base substitution G C intron_variant MELA-AU 4 146093135 146093135 single base substitution G C upstream_gene_variant MELA-AU 4 146093836 146093836 single base substitution G A intron_variant MELA-AU 4 146093836 146093836 single base substitution G A upstream_gene_variant MELA-AU 4 146094666 146094666 single base substitution G A intron_variant MELA-AU 4 146094666 146094666 single base substitution G A upstream_gene_variant MELA-AU 4 146094695 146094695 single base substitution A G intron_variant MELA-AU 4 146094695 146094695 single base substitution A G upstream_gene_variant MELA-AU 4 146095268 146095268 single base substitution C T intron_variant MELA-AU 4 146095268 146095268 single base substitution C T upstream_gene_variant MELA-AU 4 146095457 146095457 single base substitution C T intron_variant MELA-AU 4 146095457 146095457 single base substitution C T upstream_gene_variant MELA-AU 4 146095850 146095850 single base substitution A G exon_variant MELA-AU 4 146095850 146095850 single base substitution A G missense_variant I4T 11T>C MELA-AU 4 146095850 146095850 single base substitution A G missense_variant I69T 206T>C MELA-AU 4 146095850 146095850 single base substitution A G upstream_gene_variant MELA-AU 4 146097384 146097384 deletion of <=200bp A - intron_variant MELA-AU 4 146097384 146097384 deletion of <=200bp A - upstream_gene_variant MELA-AU 4 146099320 146099320 single base substitution C G intron_variant MELA-AU 4 146099320 146099320 single base substitution C G upstream_gene_variant MELA-AU 4 146099774 146099774 single base substitution T G intron_variant MELA-AU 4 146099774 146099774 single base substitution T G upstream_gene_variant MELA-AU 4 146102372 146102372 single base substitution T C upstream_gene_variant MELA-AU 4 146103441 146103441 single base substitution C T upstream_gene_variant MELA-AU 4 146103453 146103453 single base substitution T C upstream_gene_variant MELA-AU 4 146104165 146104165 single base substitution C T upstream_gene_variant MELA-AU 4 146104186 146104186 single base substitution C T upstream_gene_variant MELA-AU 4 146104950 146104950 single base substitution G A upstream_gene_variant MELA-AU 4 146105543 146105543 single base substitution C T upstream_gene_variant MELA-AU 4 146105647 146105647 single base substitution C T upstream_gene_variant MELA-AU 4 146105666 146105666 single base substitution C T upstream_gene_variant ORCA-IN 4 146040926 146040926 insertion of <=200bp - AT intron_variant ORCA-IN 4 146044914 146044914 single base substitution G C intron_variant ORCA-IN 4 146062756 146062756 single base substitution G T downstream_gene_variant ORCA-IN 4 146062756 146062756 single base substitution G T exon_variant ORCA-IN 4 146062756 146062756 single base substitution G T missense_variant Q555K 1663C>A ORCA-IN 4 146062756 146062756 single base substitution G T missense_variant Q620K 1858C>A ORCA-IN 4 146065582 146065582 single base substitution G A downstream_gene_variant ORCA-IN 4 146065582 146065582 single base substitution G A exon_variant ORCA-IN 4 146065582 146065582 single base substitution G A missense_variant S411L 1232C>T ORCA-IN 4 146065582 146065582 single base substitution G A missense_variant S476L 1427C>T ORCA-IN 4 146070872 146070872 single base substitution G C intron_variant ORCA-IN 4 146074050 146074050 deletion of <=200bp C - downstream_gene_variant ORCA-IN 4 146074050 146074050 deletion of <=200bp C - intron_variant ORCA-IN 4 146074050 146074050 deletion of <=200bp C - upstream_gene_variant ORCA-IN 4 146098818 146098818 single base substitution G T intron_variant OV-AU 4 146028343 146028343 single base substitution C T downstream_gene_variant OV-AU 4 146031815 146031815 single base substitution G C downstream_gene_variant OV-AU 4 146034242 146034242 single base substitution G A intron_variant OV-AU 4 146043817 146043817 single base substitution G C intron_variant OV-AU 4 146046418 146046418 single base substitution G C intron_variant OV-AU 4 146058016 146058016 single base substitution G A 3_prime_UTR_variant OV-AU 4 146058016 146058016 single base substitution G A downstream_gene_variant OV-AU 4 146058016 146058016 single base substitution G A intron_variant OV-AU 4 146061863 146061863 single base substitution G C intron_variant OV-AU 4 146064913 146064913 single base substitution C G downstream_gene_variant OV-AU 4 146064913 146064913 single base substitution C G intron_variant OV-AU 4 146077384 146077384 single base substitution A C downstream_gene_variant OV-AU 4 146077384 146077384 single base substitution A C intron_variant OV-AU 4 146094511 146094511 single base substitution A C intron_variant OV-AU 4 146094511 146094511 single base substitution A C upstream_gene_variant OV-AU 4 146097087 146097087 single base substitution C G intron_variant OV-AU 4 146097087 146097087 single base substitution C G upstream_gene_variant OV-AU 4 146098071 146098071 single base substitution A C intron_variant OV-AU 4 146100278 146100278 single base substitution A G intron_variant OV-AU 4 146100278 146100278 single base substitution A G upstream_gene_variant OV-US 4 146058812 146058812 single base substitution A C intron_variant OV-US 4 146058812 146058812 single base substitution A C missense_variant S1039A 3115T>G OV-US 4 146058812 146058812 single base substitution A C missense_variant S974A 2920T>G PACA-AU 4 146029345 146029345 single base substitution G T downstream_gene_variant PACA-AU 4 146030555 146030555 single base substitution G C downstream_gene_variant PACA-AU 4 146030755 146030755 single base substitution T G downstream_gene_variant PACA-AU 4 146032325 146032325 single base substitution T A intron_variant PACA-AU 4 146032991 146032991 single base substitution G A intron_variant PACA-AU 4 146038364 146038364 single base substitution G T intron_variant PACA-AU 4 146044938 146044938 single base substitution G T intron_variant PACA-AU 4 146047756 146047756 single base substitution T G intron_variant PACA-AU 4 146051622 146051622 single base substitution A G downstream_gene_variant PACA-AU 4 146051622 146051622 single base substitution A G intron_variant PACA-AU 4 146056239 146056239 single base substitution G A 3_prime_UTR_variant PACA-AU 4 146056239 146056239 single base substitution G A downstream_gene_variant PACA-AU 4 146056239 146056239 single base substitution G A intron_variant PACA-AU 4 146058157 146058157 single base substitution G C 3_prime_UTR_variant PACA-AU 4 146058157 146058157 single base substitution G C downstream_gene_variant PACA-AU 4 146058157 146058157 single base substitution G C intron_variant PACA-AU 4 146058966 146058966 single base substitution G A intron_variant PACA-AU 4 146058966 146058966 single base substitution G A synonymous_variant S922S 2766C>T PACA-AU 4 146058966 146058966 single base substitution G A synonymous_variant S987S 2961C>T PACA-AU 4 146060984 146060984 single base substitution A C intron_variant PACA-AU 4 146067274 146067274 single base substitution A C downstream_gene_variant PACA-AU 4 146067274 146067274 single base substitution A C exon_variant PACA-AU 4 146067274 146067274 single base substitution A C intron_variant PACA-AU 4 146068469 146068469 single base substitution C T intron_variant PACA-AU 4 146074049 146074049 single base substitution T C downstream_gene_variant PACA-AU 4 146074049 146074049 single base substitution T C intron_variant PACA-AU 4 146074049 146074049 single base substitution T C upstream_gene_variant PACA-AU 4 146075027 146075027 single base substitution T C downstream_gene_variant PACA-AU 4 146075027 146075027 single base substitution T C intron_variant PACA-AU 4 146075027 146075027 single base substitution T C upstream_gene_variant PACA-AU 4 146075511 146075511 single base substitution T C downstream_gene_variant PACA-AU 4 146075511 146075511 single base substitution T C intron_variant PACA-AU 4 146075511 146075511 single base substitution T C upstream_gene_variant PACA-AU 4 146077039 146077039 single base substitution C T downstream_gene_variant PACA-AU 4 146077039 146077039 single base substitution C T intron_variant PACA-AU 4 146077039 146077039 single base substitution C T upstream_gene_variant PACA-AU 4 146077947 146077947 insertion of <=200bp - AAT downstream_gene_variant PACA-AU 4 146077947 146077947 insertion of <=200bp - AAT intron_variant PACA-AU 4 146087308 146087308 single base substitution G A downstream_gene_variant PACA-AU 4 146087308 146087308 single base substitution G A intron_variant PACA-AU 4 146091678 146091678 single base substitution C T downstream_gene_variant PACA-AU 4 146091678 146091678 single base substitution C T intron_variant PACA-AU 4 146093383 146093383 single base substitution G C intron_variant PACA-AU 4 146093383 146093383 single base substitution G C upstream_gene_variant PACA-AU 4 146105524 146105524 single base substitution A C upstream_gene_variant PACA-AU 4 146105605 146105605 single base substitution G A upstream_gene_variant PACA-CA 4 146028177 146028177 single base substitution A G downstream_gene_variant PACA-CA 4 146031404 146031404 single base substitution A T downstream_gene_variant PACA-CA 4 146034348 146034348 single base substitution C A intron_variant PACA-CA 4 146039162 146039162 deletion of <=200bp A - intron_variant PACA-CA 4 146045180 146045180 single base substitution C G intron_variant PACA-CA 4 146046188 146046188 single base substitution G A intron_variant PACA-CA 4 146048460 146048460 single base substitution G T intron_variant PACA-CA 4 146052403 146052403 single base substitution C G downstream_gene_variant PACA-CA 4 146052403 146052403 single base substitution C G intron_variant PACA-CA 4 146053026 146053026 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 146053026 146053026 deletion of <=200bp T - intron_variant PACA-CA 4 146055501 146055501 single base substitution A G 3_prime_UTR_variant PACA-CA 4 146055501 146055501 single base substitution A G downstream_gene_variant PACA-CA 4 146055501 146055501 single base substitution A G intron_variant PACA-CA 4 146058027 146058027 single base substitution G T 3_prime_UTR_variant PACA-CA 4 146058027 146058027 single base substitution G T downstream_gene_variant PACA-CA 4 146058027 146058027 single base substitution G T intron_variant PACA-CA 4 146059877 146059877 single base substitution G T intron_variant PACA-CA 4 146060486 146060486 single base substitution G A intron_variant PACA-CA 4 146068438 146068438 single base substitution A G intron_variant PACA-CA 4 146072063 146072063 single base substitution A G downstream_gene_variant PACA-CA 4 146072063 146072063 single base substitution A G splice_region_variant PACA-CA 4 146072063 146072063 single base substitution A G upstream_gene_variant PACA-CA 4 146072238 146072238 deletion of <=200bp T - downstream_gene_variant PACA-CA 4 146072238 146072238 deletion of <=200bp T - intron_variant PACA-CA 4 146072238 146072238 deletion of <=200bp T - upstream_gene_variant PACA-CA 4 146081585 146081585 single base substitution T A intron_variant PACA-CA 4 146082783 146082783 single base substitution A G intron_variant PACA-CA 4 146084042 146084042 single base substitution G A intron_variant PACA-CA 4 146093744 146093744 single base substitution G A intron_variant PACA-CA 4 146093744 146093744 single base substitution G A upstream_gene_variant PACA-CA 4 146095227 146095227 single base substitution C T intron_variant PACA-CA 4 146095227 146095227 single base substitution C T upstream_gene_variant PACA-CA 4 146095879 146095879 single base substitution A T 5_prime_UTR_variant PACA-CA 4 146095879 146095879 single base substitution A T exon_variant PACA-CA 4 146095879 146095879 single base substitution A T synonymous_variant S59S 177T>A PACA-CA 4 146095879 146095879 single base substitution A T upstream_gene_variant PACA-CA 4 146095905 146095905 deletion of <=200bp A - intron_variant PACA-CA 4 146095905 146095905 deletion of <=200bp A - upstream_gene_variant PACA-CA 4 146096426 146096426 single base substitution A G intron_variant PACA-CA 4 146096426 146096426 single base substitution A G upstream_gene_variant PACA-CA 4 146097105 146097105 single base substitution G A intron_variant PACA-CA 4 146097105 146097105 single base substitution G A upstream_gene_variant PACA-CA 4 146102057 146102057 single base substitution C A upstream_gene_variant PACA-CA 4 146103310 146103310 single base substitution G A upstream_gene_variant PACA-CA 4 146106268 146106268 single base substitution A G upstream_gene_variant PAEN-AU 4 146060187 146060187 single base substitution G A intron_variant PAEN-AU 4 146100199 146100199 single base substitution T A intron_variant PAEN-AU 4 146100199 146100199 single base substitution T A upstream_gene_variant PBCA-DE 4 146036271 146036271 insertion of <=200bp - T intron_variant PBCA-DE 4 146036481 146036481 single base substitution T G intron_variant PBCA-DE 4 146043964 146043964 insertion of <=200bp - A intron_variant PBCA-DE 4 146056903 146056903 single base substitution C T 3_prime_UTR_variant PBCA-DE 4 146056903 146056903 single base substitution C T downstream_gene_variant PBCA-DE 4 146056903 146056903 single base substitution C T intron_variant PBCA-DE 4 146068178 146068178 deletion of <=200bp A - intron_variant PBCA-DE 4 146092329 146092329 insertion of <=200bp - A exon_variant PBCA-DE 4 146092329 146092329 insertion of <=200bp - A intron_variant PBCA-DE 4 146094503 146094503 single base substitution G A intron_variant PBCA-DE 4 146094503 146094503 single base substitution G A upstream_gene_variant PBCA-DE 4 146104934 146104934 insertion of <=200bp - A upstream_gene_variant PRAD-CA 4 146032100 146032100 single base substitution T G exon_variant PRAD-CA 4 146054242 146054242 single base substitution C T downstream_gene_variant PRAD-CA 4 146054242 146054242 single base substitution C T intron_variant PRAD-CA 4 146056320 146056320 single base substitution G A 3_prime_UTR_variant PRAD-CA 4 146056320 146056320 single base substitution G A downstream_gene_variant PRAD-CA 4 146056320 146056320 single base substitution G A intron_variant PRAD-CA 4 146072237 146072237 single base substitution A T downstream_gene_variant PRAD-CA 4 146072237 146072237 single base substitution A T intron_variant PRAD-CA 4 146072237 146072237 single base substitution A T upstream_gene_variant PRAD-CA 4 146078567 146078567 single base substitution G A downstream_gene_variant PRAD-CA 4 146078567 146078567 single base substitution G A intron_variant PRAD-CA 4 146079707 146079707 single base substitution T C downstream_gene_variant PRAD-CA 4 146079707 146079707 single base substitution T C intron_variant PRAD-CA 4 146098528 146098528 single base substitution A C intron_variant PRAD-UK 4 146056036 146056038 deletion of <=200bp TGG - 3_prime_UTR_variant PRAD-UK 4 146056036 146056038 deletion of <=200bp TGG - downstream_gene_variant PRAD-UK 4 146056036 146056038 deletion of <=200bp TGG - intron_variant PRAD-US 4 146032204 146032204 single base substitution A C exon_variant PRAD-US 4 146058591 146058591 single base substitution C T intron_variant PRAD-US 4 146058591 146058591 single base substitution C T synonymous_variant Q1047Q 3141G>A PRAD-US 4 146058591 146058591 single base substitution C T synonymous_variant Q1112Q 3336G>A PRAD-US 4 146058804 146058804 single base substitution C A intron_variant PRAD-US 4 146058804 146058804 single base substitution C A missense_variant Q1041H 3123G>T PRAD-US 4 146058804 146058804 single base substitution C A missense_variant Q976H 2928G>T PRAD-US 4 146058891 146058891 single base substitution A C intron_variant PRAD-US 4 146058891 146058891 single base substitution A C synonymous_variant V1012V 3036T>G PRAD-US 4 146058891 146058891 single base substitution A C synonymous_variant V947V 2841T>G PRAD-US 4 146059006 146059006 single base substitution G A intron_variant PRAD-US 4 146059006 146059006 single base substitution G A missense_variant T909I 2726C>T PRAD-US 4 146059006 146059006 single base substitution G A missense_variant T974I 2921C>T PRAD-US 4 146059041 146059041 single base substitution A G intron_variant PRAD-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C PRAD-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C PRAD-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD153D PRAD-US 4 146077123 146077125 deletion of <=200bp CAG - disruptive_inframe_deletion AD218D PRAD-US 4 146077123 146077125 deletion of <=200bp CAG - downstream_gene_variant PRAD-US 4 146077123 146077125 deletion of <=200bp CAG - exon_variant READ-US 4 146029234 146029234 single base substitution G A downstream_gene_variant READ-US 4 146064598 146064598 single base substitution C A downstream_gene_variant READ-US 4 146064598 146064598 single base substitution C A splice_acceptor_variant READ-US 4 146072024 146072024 single base substitution T G downstream_gene_variant READ-US 4 146072024 146072024 single base substitution T G exon_variant READ-US 4 146072024 146072024 single base substitution T G synonymous_variant P268P 804A>C READ-US 4 146072024 146072024 single base substitution T G synonymous_variant P269P 807A>C READ-US 4 146072024 146072024 single base substitution T G synonymous_variant P334P 1002A>C RECA-EU 4 146052036 146052036 single base substitution C T downstream_gene_variant RECA-EU 4 146052036 146052036 single base substitution C T intron_variant RECA-EU 4 146065815 146065815 single base substitution T A downstream_gene_variant RECA-EU 4 146065815 146065815 single base substitution T A intron_variant RECA-EU 4 146065825 146065825 single base substitution A T downstream_gene_variant RECA-EU 4 146065825 146065825 single base substitution A T intron_variant RECA-EU 4 146082027 146082027 single base substitution T A intron_variant RECA-EU 4 146086312 146086312 single base substitution A T exon_variant RECA-EU 4 146086312 146086312 single base substitution A T intron_variant RECA-EU 4 146086312 146086312 single base substitution A T missense_variant L111H 332T>A RECA-EU 4 146086312 146086312 single base substitution A T missense_variant L46H 137T>A RECA-EU 4 146102227 146102227 single base substitution C T upstream_gene_variant SKCA-BR 4 146032724 146032724 single base substitution C T intron_variant SKCA-BR 4 146033294 146033294 single base substitution C T intron_variant SKCA-BR 4 146034495 146034495 single base substitution C T intron_variant SKCA-BR 4 146041527 146041527 single base substitution C T intron_variant SKCA-BR 4 146046278 146046278 single base substitution C T intron_variant SKCA-BR 4 146054660 146054660 single base substitution C T downstream_gene_variant SKCA-BR 4 146054660 146054660 single base substitution C T intron_variant SKCA-BR 4 146056639 146056639 single base substitution C T 3_prime_UTR_variant SKCA-BR 4 146056639 146056639 single base substitution C T downstream_gene_variant SKCA-BR 4 146056639 146056639 single base substitution C T intron_variant SKCA-BR 4 146058167 146058167 single base substitution T C 3_prime_UTR_variant SKCA-BR 4 146058167 146058167 single base substitution T C downstream_gene_variant SKCA-BR 4 146058167 146058167 single base substitution T C intron_variant SKCA-BR 4 146058741 146058741 single base substitution A G intron_variant SKCA-BR 4 146058741 146058741 single base substitution A G synonymous_variant G1062G 3186T>C SKCA-BR 4 146058741 146058741 single base substitution A G synonymous_variant G997G 2991T>C SKCA-BR 4 146059434 146059434 single base substitution T C intron_variant SKCA-BR 4 146059434 146059434 single base substitution T C synonymous_variant L766L 2298A>G SKCA-BR 4 146059434 146059434 single base substitution T C synonymous_variant L831L 2493A>G SKCA-BR 4 146059512 146059512 single base substitution A G intron_variant SKCA-BR 4 146059512 146059512 single base substitution A G synonymous_variant H740H 2220T>C SKCA-BR 4 146059512 146059512 single base substitution A G synonymous_variant H805H 2415T>C SKCA-BR 4 146061774 146061774 single base substitution C A intron_variant SKCA-BR 4 146061806 146061806 single base substitution A C intron_variant SKCA-BR 4 146063400 146063400 single base substitution T G downstream_gene_variant SKCA-BR 4 146063400 146063400 single base substitution T G exon_variant SKCA-BR 4 146063400 146063400 single base substitution T G missense_variant L525F 1575A>C SKCA-BR 4 146063400 146063400 single base substitution T G missense_variant L590F 1770A>C SKCA-BR 4 146070524 146070524 single base substitution G A intron_variant SKCA-BR 4 146078829 146078829 single base substitution T C downstream_gene_variant SKCA-BR 4 146078829 146078829 single base substitution T C intron_variant SKCA-BR 4 146079900 146079900 single base substitution A C downstream_gene_variant SKCA-BR 4 146079900 146079900 single base substitution A C intron_variant SKCA-BR 4 146084313 146084313 single base substitution G A intron_variant SKCA-BR 4 146086197 146086197 single base substitution A C intron_variant SKCA-BR 4 146087240 146087240 single base substitution G A downstream_gene_variant SKCA-BR 4 146087240 146087240 single base substitution G A intron_variant SKCA-BR 4 146095158 146095158 insertion of <=200bp - AT intron_variant SKCA-BR 4 146095158 146095158 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 4 146095986 146095986 single base substitution A G intron_variant SKCA-BR 4 146095986 146095986 single base substitution A G upstream_gene_variant SKCA-BR 4 146099397 146099397 single base substitution G A intron_variant SKCA-BR 4 146099397 146099397 single base substitution G A upstream_gene_variant SKCA-BR 4 146100946 146100946 single base substitution T C intron_variant SKCA-BR 4 146100946 146100946 single base substitution T C upstream_gene_variant SKCA-BR 4 146101508 146101508 single base substitution A C upstream_gene_variant SKCA-BR 4 146101792 146101792 single base substitution A G upstream_gene_variant SKCA-BR 4 146105074 146105074 single base substitution C T upstream_gene_variant SKCA-BR 4 146105570 146105570 single base substitution C T upstream_gene_variant SKCA-BR 4 146106051 146106051 single base substitution C T upstream_gene_variant SKCA-BR 4 146106312 146106312 single base substitution C T upstream_gene_variant SKCM-US 4 146029175 146029175 single base substitution C T downstream_gene_variant SKCM-US 4 146029233 146029233 single base substitution C T downstream_gene_variant SKCM-US 4 146030294 146030294 single base substitution C T downstream_gene_variant SKCM-US 4 146031360 146031360 single base substitution C T downstream_gene_variant SKCM-US 4 146032131 146032131 single base substitution C T exon_variant SKCM-US 4 146042490 146042490 single base substitution G A intron_variant SKCM-US 4 146042539 146042539 single base substitution C T intron_variant SKCM-US 4 146044172 146044172 single base substitution G A intron_variant SKCM-US 4 146044254 146044254 single base substitution C T intron_variant SKCM-US 4 146044633 146044633 single base substitution C T intron_variant SKCM-US 4 146059006 146059006 single base substitution G A intron_variant SKCM-US 4 146059006 146059006 single base substitution G A missense_variant T909I 2726C>T SKCM-US 4 146059006 146059006 single base substitution G A missense_variant T974I 2921C>T SKCM-US 4 146059041 146059041 single base substitution A G intron_variant SKCM-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C SKCM-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C SKCM-US 4 146062615 146062615 single base substitution G A downstream_gene_variant SKCM-US 4 146062615 146062615 single base substitution G A exon_variant SKCM-US 4 146062615 146062615 single base substitution G A missense_variant P602S 1804C>T SKCM-US 4 146062615 146062615 single base substitution G A missense_variant P667S 1999C>T SKCM-US 4 146064533 146064533 single base substitution G A downstream_gene_variant SKCM-US 4 146064533 146064533 single base substitution G A exon_variant SKCM-US 4 146064533 146064533 single base substitution G A missense_variant P491L 1472C>T SKCM-US 4 146064533 146064533 single base substitution G A missense_variant P556L 1667C>T SKCM-US 4 146065546 146065546 single base substitution G A downstream_gene_variant SKCM-US 4 146065546 146065546 single base substitution G A exon_variant SKCM-US 4 146065546 146065546 single base substitution G A missense_variant P423L 1268C>T SKCM-US 4 146065546 146065546 single base substitution G A missense_variant P488L 1463C>T SKCM-US 4 146067419 146067419 single base substitution G A downstream_gene_variant SKCM-US 4 146067419 146067419 single base substitution G A exon_variant SKCM-US 4 146067419 146067419 single base substitution G A splice_region_variant SKCM-US 4 146067531 146067531 single base substitution G A exon_variant SKCM-US 4 146067531 146067531 single base substitution G A missense_variant S371F 1112C>T SKCM-US 4 146067531 146067531 single base substitution G A missense_variant S372F 1115C>T SKCM-US 4 146067531 146067531 single base substitution G A missense_variant S437F 1310C>T SKCM-US 4 146071734 146071734 single base substitution G C exon_variant SKCM-US 4 146071734 146071734 single base substitution G C stop_gained S331* 992C>G SKCM-US 4 146071734 146071734 single base substitution G C stop_gained S332* 995C>G SKCM-US 4 146071734 146071734 single base substitution G C stop_gained S397* 1190C>G SKCM-US 4 146071774 146071774 single base substitution G A exon_variant SKCM-US 4 146071774 146071774 single base substitution G A missense_variant P318S 952C>T SKCM-US 4 146071774 146071774 single base substitution G A missense_variant P319S 955C>T SKCM-US 4 146071774 146071774 single base substitution G A missense_variant P384S 1150C>T SKCM-US 4 146071980 146071980 single base substitution G A downstream_gene_variant SKCM-US 4 146071980 146071980 single base substitution G A exon_variant SKCM-US 4 146071980 146071980 single base substitution G A missense_variant S283F 848C>T SKCM-US 4 146071980 146071980 single base substitution G A missense_variant S284F 851C>T SKCM-US 4 146071980 146071980 single base substitution G A missense_variant S349F 1046C>T SKCM-US 4 146072028 146072028 single base substitution G A downstream_gene_variant SKCM-US 4 146072028 146072028 single base substitution G A exon_variant SKCM-US 4 146072028 146072028 single base substitution G A missense_variant P267L 800C>T SKCM-US 4 146072028 146072028 single base substitution G A missense_variant P268L 803C>T SKCM-US 4 146072028 146072028 single base substitution G A missense_variant P333L 998C>T SKCM-US 4 146076605 146076605 single base substitution G A downstream_gene_variant SKCM-US 4 146076605 146076605 single base substitution G A exon_variant SKCM-US 4 146076605 146076605 single base substitution G A synonymous_variant S211S 633C>T SKCM-US 4 146076605 146076605 single base substitution G A synonymous_variant S212S 636C>T SKCM-US 4 146076605 146076605 single base substitution G A synonymous_variant S277S 831C>T SKCM-US 4 146076605 146076605 single base substitution G A upstream_gene_variant SKCM-US 4 146086315 146086315 single base substitution G A exon_variant SKCM-US 4 146086315 146086315 single base substitution G A intron_variant SKCM-US 4 146086315 146086315 single base substitution G A missense_variant S110F 329C>T SKCM-US 4 146086315 146086315 single base substitution G A missense_variant S45F 134C>T STAD-US 4 146041093 146041093 deletion of <=200bp T - intron_variant STAD-US 4 146041224 146041224 deletion of <=200bp A - intron_variant STAD-US 4 146041302 146041302 single base substitution A T intron_variant STAD-US 4 146044706 146044706 single base substitution G A intron_variant STAD-US 4 146058622 146058624 deletion of <=200bp CTC - disruptive_inframe_deletion RR1036R STAD-US 4 146058622 146058624 deletion of <=200bp CTC - disruptive_inframe_deletion RR1101R STAD-US 4 146058622 146058624 deletion of <=200bp CTC - intron_variant STAD-US 4 146059018 146059018 single base substitution C G intron_variant STAD-US 4 146059018 146059018 single base substitution C G missense_variant R905T 2714G>C STAD-US 4 146059018 146059018 single base substitution C G missense_variant R970T 2909G>C STAD-US 4 146059083 146059083 single base substitution C T intron_variant STAD-US 4 146059083 146059083 single base substitution C T synonymous_variant T883T 2649G>A STAD-US 4 146059083 146059083 single base substitution C T synonymous_variant T948T 2844G>A STAD-US 4 146059097 146059097 single base substitution G A intron_variant STAD-US 4 146059097 146059097 single base substitution G A stop_gained R879* 2635C>T STAD-US 4 146059097 146059097 single base substitution G A stop_gained R944* 2830C>T STAD-US 4 146059221 146059221 single base substitution A G intron_variant STAD-US 4 146059221 146059221 single base substitution A G synonymous_variant D837D 2511T>C STAD-US 4 146059221 146059221 single base substitution A G synonymous_variant D902D 2706T>C STAD-US 4 146059262 146059262 single base substitution C T intron_variant STAD-US 4 146059262 146059262 single base substitution C T missense_variant E824K 2470G>A STAD-US 4 146059262 146059262 single base substitution C T missense_variant E889K 2665G>A STAD-US 4 146059468 146059468 single base substitution C T intron_variant STAD-US 4 146059468 146059468 single base substitution C T missense_variant G755E 2264G>A STAD-US 4 146059468 146059468 single base substitution C T missense_variant G820E 2459G>A STAD-US 4 146064586 146064586 single base substitution A G downstream_gene_variant STAD-US 4 146064586 146064586 single base substitution A G exon_variant STAD-US 4 146064586 146064586 single base substitution A G synonymous_variant D473D 1419T>C STAD-US 4 146064586 146064586 single base substitution A G synonymous_variant D538D 1614T>C STAD-US 4 146065564 146065564 single base substitution G T downstream_gene_variant STAD-US 4 146065564 146065564 single base substitution G T exon_variant STAD-US 4 146065564 146065564 single base substitution G T missense_variant A417D 1250C>A STAD-US 4 146065564 146065564 single base substitution G T missense_variant A482D 1445C>A STAD-US 4 146067479 146067479 single base substitution T G downstream_gene_variant STAD-US 4 146067479 146067479 single base substitution T G exon_variant STAD-US 4 146067479 146067479 single base substitution T G missense_variant E389D 1167A>C STAD-US 4 146067479 146067479 single base substitution T G missense_variant E454D 1362A>C STAD-US 4 146071750 146071750 single base substitution A G exon_variant STAD-US 4 146071750 146071750 single base substitution A G missense_variant F326L 976T>C STAD-US 4 146071750 146071750 single base substitution A G missense_variant F327L 979T>C STAD-US 4 146071750 146071750 single base substitution A G missense_variant F392L 1174T>C STAD-US 4 146071793 146071793 deletion of <=200bp T - exon_variant STAD-US 4 146071793 146071793 deletion of <=200bp T - frameshift_variant L311 STAD-US 4 146071793 146071793 deletion of <=200bp T - frameshift_variant L312 STAD-US 4 146071793 146071793 deletion of <=200bp T - frameshift_variant L377 STAD-US 4 146071816 146071816 single base substitution G A exon_variant STAD-US 4 146071816 146071816 single base substitution G A missense_variant P304S 910C>T STAD-US 4 146071816 146071816 single base substitution G A missense_variant P305S 913C>T STAD-US 4 146071816 146071816 single base substitution G A missense_variant P370S 1108C>T STAD-US 4 146071967 146071967 single base substitution T G downstream_gene_variant STAD-US 4 146071967 146071967 single base substitution T G exon_variant STAD-US 4 146071967 146071967 single base substitution T G missense_variant Q287H 861A>C STAD-US 4 146071967 146071967 single base substitution T G missense_variant Q288H 864A>C STAD-US 4 146071967 146071967 single base substitution T G missense_variant Q353H 1059A>C STAD-US 4 146071986 146071986 single base substitution T G downstream_gene_variant STAD-US 4 146071986 146071986 single base substitution T G exon_variant STAD-US 4 146071986 146071986 single base substitution T G missense_variant K281T 842A>C STAD-US 4 146071986 146071986 single base substitution T G missense_variant K282T 845A>C STAD-US 4 146071986 146071986 single base substitution T G missense_variant K347T 1040A>C THCA-SA 4 146056320 146056320 single base substitution G A 3_prime_UTR_variant THCA-SA 4 146056320 146056320 single base substitution G A downstream_gene_variant THCA-SA 4 146056320 146056320 single base substitution G A intron_variant THCA-US 4 146059006 146059006 single base substitution G A intron_variant THCA-US 4 146059006 146059006 single base substitution G A missense_variant T909I 2726C>T THCA-US 4 146059006 146059006 single base substitution G A missense_variant T974I 2921C>T THCA-US 4 146059041 146059041 single base substitution A G intron_variant THCA-US 4 146059041 146059041 single base substitution A G synonymous_variant H897H 2691T>C THCA-US 4 146059041 146059041 single base substitution A G synonymous_variant H962H 2886T>C UCEC-US 4 146029243 146029243 single base substitution C T downstream_gene_variant UCEC-US 4 146030400 146030400 single base substitution A T downstream_gene_variant UCEC-US 4 146031299 146031299 single base substitution T G downstream_gene_variant UCEC-US 4 146032180 146032180 single base substitution T G exon_variant UCEC-US 4 146038505 146038505 single base substitution C T intron_variant UCEC-US 4 146041162 146041162 single base substitution C T intron_variant UCEC-US 4 146044182 146044182 single base substitution C T intron_variant UCEC-US 4 146044712 146044712 single base substitution G A intron_variant UCEC-US 4 146048713 146048713 single base substitution C A intron_variant UCEC-US 4 146058955 146058955 single base substitution T G intron_variant UCEC-US 4 146058955 146058955 single base substitution T G missense_variant K926T 2777A>C UCEC-US 4 146058955 146058955 single base substitution T G missense_variant K991T 2972A>C UCEC-US 4 146058959 146058959 single base substitution C A intron_variant UCEC-US 4 146058959 146058959 single base substitution C A stop_gained E925* 2773G>T UCEC-US 4 146058959 146058959 single base substitution C A stop_gained E990* 2968G>T UCEC-US 4 146059132 146059132 single base substitution G A intron_variant UCEC-US 4 146059132 146059132 single base substitution G A missense_variant P867L 2600C>T UCEC-US 4 146059132 146059132 single base substitution G A missense_variant P932L 2795C>T UCEC-US 4 146059133 146059133 single base substitution G A intron_variant UCEC-US 4 146059133 146059133 single base substitution G A missense_variant P867S 2599C>T UCEC-US 4 146059133 146059133 single base substitution G A missense_variant P932S 2794C>T UCEC-US 4 146059239 146059239 single base substitution A G intron_variant UCEC-US 4 146059239 146059239 single base substitution A G synonymous_variant N831N 2493T>C UCEC-US 4 146059239 146059239 single base substitution A G synonymous_variant N896N 2688T>C UCEC-US 4 146059262 146059262 single base substitution C A intron_variant UCEC-US 4 146059262 146059262 single base substitution C A stop_gained E824* 2470G>T UCEC-US 4 146059262 146059262 single base substitution C A stop_gained E889* 2665G>T UCEC-US 4 146059564 146059564 single base substitution G A intron_variant UCEC-US 4 146059564 146059564 single base substitution G A missense_variant P723L 2168C>T UCEC-US 4 146059564 146059564 single base substitution G A missense_variant P788L 2363C>T UCEC-US 4 146062584 146062584 single base substitution C T downstream_gene_variant UCEC-US 4 146062584 146062584 single base substitution C T exon_variant UCEC-US 4 146062584 146062584 single base substitution C T missense_variant R612Q 1835G>A UCEC-US 4 146062584 146062584 single base substitution C T missense_variant R677Q 2030G>A UCEC-US 4 146064538 146064538 single base substitution C T downstream_gene_variant UCEC-US 4 146064538 146064538 single base substitution C T exon_variant UCEC-US 4 146064538 146064538 single base substitution C T synonymous_variant E489E 1467G>A UCEC-US 4 146064538 146064538 single base substitution C T synonymous_variant E554E 1662G>A UCEC-US 4 146064547 146064547 single base substitution C T downstream_gene_variant UCEC-US 4 146064547 146064547 single base substitution C T exon_variant UCEC-US 4 146064547 146064547 single base substitution C T synonymous_variant K486K 1458G>A UCEC-US 4 146064547 146064547 single base substitution C T synonymous_variant K551K 1653G>A UCEC-US 4 146067458 146067458 single base substitution C A downstream_gene_variant UCEC-US 4 146067458 146067458 single base substitution C A exon_variant UCEC-US 4 146067458 146067458 single base substitution C A missense_variant E396D 1188G>T UCEC-US 4 146067458 146067458 single base substitution C A missense_variant E461D 1383G>T UCEC-US 4 146067564 146067564 single base substitution C A exon_variant UCEC-US 4 146067564 146067564 single base substitution C A missense_variant R360I 1079G>T UCEC-US 4 146067564 146067564 single base substitution C A missense_variant R361I 1082G>T UCEC-US 4 146067564 146067564 single base substitution C A missense_variant R426I 1277G>T UCEC-US 4 146071745 146071745 single base substitution A G exon_variant UCEC-US 4 146071745 146071745 single base substitution A G synonymous_variant S327S 981T>C UCEC-US 4 146071745 146071745 single base substitution A G synonymous_variant S328S 984T>C UCEC-US 4 146071745 146071745 single base substitution A G synonymous_variant S393S 1179T>C UCEC-US 4 146071750 146071750 single base substitution A G exon_variant UCEC-US 4 146071750 146071750 single base substitution A G missense_variant F326L 976T>C UCEC-US 4 146071750 146071750 single base substitution A G missense_variant F327L 979T>C UCEC-US 4 146071750 146071750 single base substitution A G missense_variant F392L 1174T>C UCEC-US 4 146071810 146071810 single base substitution T G exon_variant UCEC-US 4 146071810 146071810 single base substitution T G missense_variant K306Q 916A>C UCEC-US 4 146071810 146071810 single base substitution T G missense_variant K307Q 919A>C UCEC-US 4 146071810 146071810 single base substitution T G missense_variant K372Q 1114A>C UCEC-US 4 146072045 146072045 single base substitution C A downstream_gene_variant UCEC-US 4 146072045 146072045 single base substitution C A exon_variant UCEC-US 4 146072045 146072045 single base substitution C A missense_variant K261N 783G>T UCEC-US 4 146072045 146072045 single base substitution C A missense_variant K262N 786G>T UCEC-US 4 146072045 146072045 single base substitution C A missense_variant K327N 981G>T UCEC-US 4 146073706 146073706 single base substitution C A downstream_gene_variant UCEC-US 4 146073706 146073706 single base substitution C A exon_variant UCEC-US 4 146073706 146073706 single base substitution C A stop_gained E253* 757G>T UCEC-US 4 146073706 146073706 single base substitution C A stop_gained E254* 760G>T UCEC-US 4 146073706 146073706 single base substitution C A stop_gained E319* 955G>T UCEC-US 4 146073706 146073706 single base substitution C A upstream_gene_variant UCEC-US 4 146073719 146073719 single base substitution T G downstream_gene_variant UCEC-US 4 146073719 146073719 single base substitution T G exon_variant UCEC-US 4 146073719 146073719 single base substitution T G synonymous_variant P248P 744A>C UCEC-US 4 146073719 146073719 single base substitution T G synonymous_variant P249P 747A>C UCEC-US 4 146073719 146073719 single base substitution T G synonymous_variant P314P 942A>C UCEC-US 4 146073719 146073719 single base substitution T G upstream_gene_variant UCEC-US 4 146077089 146077089 single base substitution T G downstream_gene_variant UCEC-US 4 146077089 146077089 single base substitution T G missense_variant E165A 494A>C UCEC-US 4 146077089 146077089 single base substitution T G missense_variant E230A 689A>C UCEC-US 4 146077089 146077089 single base substitution T G splice_region_variant UCEC-US 4 146085374 146085374 single base substitution C A exon_variant UCEC-US 4 146085374 146085374 single base substitution C A missense_variant D116Y 346G>T UCEC-US 4 146085374 146085374 single base substitution C A missense_variant D51Y 151G>T UCEC-US 4 146092862 146092862 single base substitution C T exon_variant UCEC-US 4 146092862 146092862 single base substitution C T missense_variant G20E 59G>A UCEC-US 4 146092862 146092862 single base substitution C T missense_variant G85E 254G>A UCEC-US 4 146095839 146095839 single base substitution G A exon_variant UCEC-US 4 146095839 146095839 single base substitution G A stop_gained R73* 217C>T UCEC-US 4 146095839 146095839 single base substitution G A stop_gained R8* 22C>T UCEC-US 4 146095839 146095839 single base substitution G A upstream_gene_variant UCEC-US 4 146095877 146095877 single base substitution C T 5_prime_UTR_variant UCEC-US 4 146095877 146095877 single base substitution C T exon_variant UCEC-US 4 146095877 146095877 single base substitution C T missense_variant R60H 179G>A UCEC-US 4 146095877 146095877 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand V-PH-04T COSM4770297 c.247C>T p.H83Y Substitution - Missense 4:145162694-145162694 - TCGA-C5-A1BF-01 COSM4836749 c.2322G>A p.Q774Q Substitution - coding silent 4:145138258-145138258 - TCGA-24-2281-01 COSM72043 c.3004G>T p.V1002L Substitution - Missense 4:145137576-145137576 - CHC909T COSM4806311 c.2758A>G p.I920V Substitution - Missense 4:145137822-145137822 - QGP1 COSM3126721 c.1238T>C p.V413A Substitution - Missense 4:145144424-145144424 - TCGA-AP-A0LM-01 COSM4873357 c.2688T>C p.N896N Substitution - coding silent 4:145138087-145138087 - EW8 COSM3126753 c.691C>A p.Q231K Substitution - Missense 4:145155686-145155686 - ESCC_113 COSM5639611 c.1104C>A p.S368R Substitution - Missense 4:145150668-145150668 - TCGA-FC-7708-01 COSM3783787 c.3036T>G p.V1012V Substitution - coding silent 4:145137739-145137739 - TCGA-EE-A29M-06 COSM3600641 c.1268C>T p.P423L Substitution - Missense 4:145144394-145144394 - RK029_C01 COSM1633478 c.160-5T>G p.? Unknown 4:145174749-145174749 - B85-2 COSM1753560 c.1499G>A p.R500K Substitution - Missense 4:145144358-145144358 - TCGA-D8-A1JA-01 COSM3825283 c.2651C>T p.S884F Substitution - Missense 4:145138124-145138124 - TCGA-EJ-7789-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-EM-A3AQ-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - Pat_53_A COSM5091532 c.458_460delCTG p.A153delA Deletion - In frame 4:145155971-145155973 - I2L-P24Tb-Tumor-Biopsy COSM5356043 c.1699G>A p.V567M Substitution - Missense 4:145142319-145142319 - TCGA-BR-8297-01 COSM4122553 c.1362A>C p.E454D Substitution - Missense 4:145146327-145146327 - C547 COSM4442508 c.1262G>A p.S421N Substitution - Missense 4:145144400-145144400 - sysucc-311T COSM5466063 c.36G>T p.E12D Substitution - Missense 4:145174673-145174673 - TCGA-66-2785-01 COSM732487 c.432C>G p.C144W Substitution - Missense 4:145159505-145159505 - TCGA-EM-A3AQ-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - S00944 COSM313829 c.32G>T p.R11I Substitution - Missense 4:145174677-145174677 - BD189T COSM5508321 c.2488G>A p.E830K Substitution - Missense 4:145138092-145138092 - Case5a COSM1717136 c.608A>G p.K203R Substitution - Missense 4:145155574-145155574 - TCGA-B0-5110-01 COSM480918 c.1525C>T p.P509S Substitution - Missense 4:145142298-145142298 - TCGA-EE-A2MI-06 COSM3600653 c.636C>T p.S212S Substitution - coding silent 4:145155453-145155453 - TCGA-B5-A11E-01 COSM4870295 c.346G>T p.D116Y Substitution - Missense 4:145164222-145164222 - TCGA-FG-7634-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - XHDG27 COSM4769150 c.1345G>A p.E449K Substitution - Missense 4:145146344-145146344 - CHEWS023 COSM4584822 c.2611C>T p.R871W Substitution - Missense 4:145137969-145137969 - BD189T COSM5508322 c.2683G>A p.E895K Substitution - Missense 4:145138092-145138092 - TCGA-D1-A16F-01 COSM1051729 c.2168C>T p.P723L Substitution - Missense 4:145138412-145138412 - TCGA-BR-6452-01 COSM4122542 c.2511T>C p.D837D Substitution - coding silent 4:145138069-145138069 - TCGA-G4-6628-01 COSM1427350 c.3134G>T p.R1045M Substitution - Missense 4:145137446-145137446 - 2290929 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-DK-A1AC-01 COSM4811804 c.1360G>A p.E454K Substitution - Missense 4:145146329-145146329 - BD136T COSM5507538 c.497-7A>T p.? Unknown 4:145159642-145159642 - 587342 COSM1219000 c.1097A>G p.D366G Substitution - Missense 4:145146397-145146397 - 2492723 COSM5723741 c.1150G>T p.E384* Substitution - Nonsense 4:145146344-145146344 - TCGA-DU-8158-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - TCGA-10-0930-01 COSM75809 c.2920T>G p.S974A Substitution - Missense 4:145137660-145137660 - TCGA-CH-5766-01 COSM4879521 c.3123G>T p.Q1041H Substitution - Missense 4:145137652-145137652 - TCGA-BR-4184-01 COSM1051743 c.979T>C p.F327L Substitution - Missense 4:145150598-145150598 - TCGA-FD-A3NA-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - Case5f COSM1717136 c.608A>G p.K203R Substitution - Missense 4:145155574-145155574 - TCGA-B5-A11U-01 COSM4871177 c.2795C>T p.P932L Substitution - Missense 4:145137980-145137980 - 2492710 COSM5718363 c.2119G>T p.V707L Substitution - Missense 4:145139956-145139956 - I2L-P24Ta-Tumor-Biopsy COSM5356043 c.1699G>A p.V567M Substitution - Missense 4:145142319-145142319 - TCGA-AP-A056-01 COSM4868407 c.955G>T p.E319* Substitution - Nonsense 4:145152554-145152554 - S02249 COSM5680158 c.2426C>G p.S809C Substitution - Missense 4:145138349-145138349 - OSCC-GB_00670111 COSM4883882 c.1858C>A p.Q620K Substitution - Missense 4:145141604-145141604 - TCGA-HC-7230-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-B5-A11E-01 COSM1594289 c.179G>A p.R60H Substitution - Missense 4:145174725-145174725 - TCGA-AX-A05Z-01 COSM1051743 c.979T>C p.F327L Substitution - Missense 4:145150598-145150598 - TCGA-CD-A4MG-01 COSM4122540 c.2635C>T p.R879* Substitution - Nonsense 4:145137945-145137945 - QGP1 COSM3126722 c.1433T>C p.V478A Substitution - Missense 4:145144424-145144424 - Pat_14_B COSM5865826 c.1670C>T p.S557F Substitution - Missense 4:145143378-145143378 - TCGA-D1-A17Q-01 COSM1051731 c.1835G>A p.R612Q Substitution - Missense 4:145141432-145141432 - TCGA-19-5954-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - CHEWS023 COSM4584823 c.2806C>T p.R936W Substitution - Missense 4:145137969-145137969 - TCGA-66-2763-01 COSM732488 c.716A>T p.D239V Substitution - Missense 4:145152598-145152598 - TCGA-AH-6544-01 COSM1566989 c.807A>C p.P269P Substitution - coding silent 4:145150872-145150872 - RK029_C COSM1633478 c.160-5T>G p.? Unknown 4:145174749-145174749 - TCGA-DK-A1AC-01 COSM1309777 c.1165G>A p.E389K Substitution - Missense 4:145146329-145146329 - TCGA-BH-A1F8-01 COSM1485712 c.1099C>T p.H367Y Substitution - Missense 4:145146395-145146395 - Hs-578-T COSM33544 c.679-2A>G p.? Unknown 4:145152637-145152637 - TCGA-DK-A1A6-01 COSM1309776 c.1617T>C p.F539F Substitution - coding silent 4:145142206-145142206 - TCGA-32-2634-01 COSM3409073 c.2167C>T p.P723S Substitution - Missense 4:145138608-145138608 - TCGA-GV-A3JZ-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-FC-7708-01 COSM3783786 c.2841T>G p.V947V Substitution - coding silent 4:145137739-145137739 - TCGA-EM-A3AQ-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - S00944 COSM5664211 c.227G>T p.R76I Substitution - Missense 4:145174677-145174677 - I2L-P24Tb-Tumor-Organoid COSM5356042 c.1504G>A p.V502M Substitution - Missense 4:145142319-145142319 - 661-06-01TD COSM5418928 c.2931C>A p.F977L Substitution - Missense 4:145137649-145137649 - TCGA-22-4591-01 COSM732489 c.1075C>G p.R359G Substitution - Missense 4:145146419-145146419 - TCGA-EE-A3JA-06 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - CHC1746T COSM4787908 c.917T>C p.I306T Substitution - Missense 4:145150660-145150660 - TCGA-EL-A3CN-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - 52 COSM5734703 c.1427C>A p.S476* Substitution - Nonsense 4:145144430-145144430 - Pat_36_B COSM5865823 c.1814delG p.G605fs*14 Deletion - Frameshift 4:145142204-145142204 - RMS66_ COSM4988110 c.1313G>T p.S438I Substitution - Missense 4:145144349-145144349 - RH18C COSM3126751 c.731C>T p.S244F Substitution - Missense 4:145155646-145155646 - BD225T COSM5508683 c.1834C>A p.R612R Substitution - coding silent 4:145141433-145141433 - TCGA-EM-A3AQ-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - T2269 COSM1427351 c.3071G>A p.R1024Q Substitution - Missense 4:145137509-145137509 - S00944 COSM313829 c.32G>T p.R11I Substitution - Missense 4:145174677-145174677 - TCGA-GV-A3JW-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-BH-A1F8-01 COSM4813373 c.1294C>T p.H432Y Substitution - Missense 4:145146395-145146395 - PT44 COSM5926476 c.2977G>A p.E993K Substitution - Missense 4:145137798-145137798 - Case5h COSM1717136 c.608A>G p.K203R Substitution - Missense 4:145155574-145155574 - 2290930 COSM1723213 c.2961C>T p.S987S Substitution - coding silent 4:145137814-145137814 - 55 COSM5014457 c.358G>T p.V120L Substitution - Missense 4:145159579-145159579 - TCGA-CG-5721-01 COSM4122547 c.2459G>A p.G820E Substitution - Missense 4:145138316-145138316 - Pat_65_A COSM5091532 c.458_460delCTG p.A153delA Deletion - In frame 4:145155971-145155973 - Case5e COSM1717136 c.608A>G p.K203R Substitution - Missense 4:145155574-145155574 - TCGA-B5-A11E-01 COSM1051755 c.151G>T p.D51Y Substitution - Missense 4:145164222-145164222 - J46_T COSM3946043 c.1090G>C p.D364H Substitution - Missense 4:145146404-145146404 - PT25 COSM5943238 c.614-6delT p.? Unknown 4:145155481-145155481 - TCGA-HU-A4G8-01 COSM4122555 c.913C>T p.P305S Substitution - Missense 4:145150664-145150664 - TCGA-AP-A0LM-01 COSM4872976 c.981G>T p.K327N Substitution - Missense 4:145150893-145150893 - 2_RESISTANT COSM1723212 c.2766C>T p.S922S Substitution - coding silent 4:145137814-145137814 - TCGA-EJ-7782-01 COSM3783784 c.3141G>A p.Q1047Q Substitution - coding silent 4:145137439-145137439 - TCGA-22-4591-01 COSM4859070 c.1270C>G p.R424G Substitution - Missense 4:145146419-145146419 - TCGA-CA-6717-01 COSM3696354 c.2110A>C p.N704H Substitution - Missense 4:145139965-145139965 - TCGA-DJ-A3UX-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - TCGA-HU-A4GU-01 COSM4122537 c.2909G>C p.R970T Substitution - Missense 4:145137866-145137866 - Case5c COSM1717136 c.608A>G p.K203R Substitution - Missense 4:145155574-145155574 - OSCC-GB_01060111 COSM4883058 c.1427C>T p.S476L Substitution - Missense 4:145144430-145144430 - BD188T COSM3126735 c.1173G>A p.A391A Substitution - coding silent 4:145150599-145150599 - Pat_53_B COSM5091533 c.653_655delCTG p.A218delA Deletion - In frame 4:145155971-145155973 - TCGA-AO-A1KP-01 COSM1485711 c.2487G>A p.L829L Substitution - coding silent 4:145138093-145138093 - LIM1899 COSM4640580 c.775C>T p.H259Y Substitution - Missense 4:145150904-145150904 - 2290930 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - TCGA-DU-8158-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - TCGA-CH-5766-01 COSM1131237 c.2928G>T p.Q976H Substitution - Missense 4:145137652-145137652 - BZ32 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - TCGA-FK-A3SH-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - SNU-C4 COSM4653769 c.1592C>T p.A531V Substitution - Missense 4:145142231-145142231 - TCGA-10-0930-01 COSM4946728 c.3115T>G p.S1039A Substitution - Missense 4:145137660-145137660 - CSCC-57-T COSM4467223 c.1672C>T p.P558S Substitution - Missense 4:145143376-145143376 - BZ32 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - TCGA-AX-A05Z-01 COSM4863651 c.1653G>A p.K551K Substitution - coding silent 4:145143395-145143395 - Pat_70_B COSM5091533 c.653_655delCTG p.A218delA Deletion - In frame 4:145155971-145155973 - I2L-P24Ta-Tumor-Biopsy COSM5356054 c.879G>T p.R293S Substitution - Missense 4:145152630-145152630 - 234 COSM3730917 c.259G>A p.V87M Substitution - Missense 4:145162682-145162682 - TCGA-24-1556-01 COSM117193 c.99G>T p.Q33H Substitution - Missense 4:145171670-145171670 - C008 COSM5523378 c.2627C>T p.S876F Substitution - Missense 4:145137953-145137953 - T3091 COSM4710571 c.2594G>A p.S865N Substitution - Missense 4:145137986-145137986 - TCGA-AP-A059-01 COSM1051739 c.1082G>T p.R361I Substitution - Missense 4:145146412-145146412 - NB-1977 COSM1286930 c.1481C>T p.A494V Substitution - Missense 4:145143372-145143372 - 2492722 COSM5723741 c.1150G>T p.E384* Substitution - Nonsense 4:145146344-145146344 - TCGA-06-0216-01 COSM2150937 c.465G>A p.V155V Substitution - coding silent 4:145155966-145155966 - TCGA-AO-A1KP-01 COSM4814456 c.2682G>A p.L894L Substitution - coding silent 4:145138093-145138093 - TCGA-AX-A05Z-01 COSM1051735 c.1458G>A p.K486K Substitution - coding silent 4:145143395-145143395 - I2L-P24Ta-Tumor-Biopsy COSM5356042 c.1504G>A p.V502M Substitution - Missense 4:145142319-145142319 - 522_T COSM3946046 c.352A>G p.I118V Substitution - Missense 4:145164216-145164216 - CSCC-11-T COSM4477364 c.2341C>T p.P781S Substitution - Missense 4:145138434-145138434 - TCGA-DK-A1AD-01 COSM4812322 c.1333G>A p.E445K Substitution - Missense 4:145146356-145146356 - Pat_53_A COSM5091533 c.653_655delCTG p.A218delA Deletion - In frame 4:145155971-145155973 - TCGA-BS-A0UF-01 COSM1051759 c.22C>T p.R8* Substitution - Nonsense 4:145174687-145174687 - I2L-P7-Tumor-Organoid COSM4710566 c.3086G>A p.R1029Q Substitution - Missense 4:145137494-145137494 - TCGA-AA-A010-01 COSM283657 c.1774A>G p.T592A Substitution - Missense 4:145141493-145141493 - 2492721 COSM5723742 c.1345G>T p.E449* Substitution - Nonsense 4:145146344-145146344 - CHC197T COSM3669213 c.1870A>G p.T624A Substitution - Missense 4:145141592-145141592 - CSCC-55-T COSM4512488 c.904C>T p.P302S Substitution - Missense 4:145150673-145150673 - TCGA-AX-A0J1-01 COSM1051721 c.2599C>T p.P867S Substitution - Missense 4:145137981-145137981 - TCGA-AX-A05Z-01 COSM4122554 c.1174T>C p.F392L Substitution - Missense 4:145150598-145150598 - TCGA-BR-8680-01 COSM4122560 c.1040A>C p.K347T Substitution - Missense 4:145150834-145150834 - TCGA-FJ-A3ZF-01 COSM3775587 c.2938C>T p.Q980* Substitution - Nonsense 4:145137642-145137642 - TCGA-56-5898-01 COSM4863057 c.1673C>T p.P558L Substitution - Missense 4:145143375-145143375 - TCGA-EE-A20C-06 COSM3600646 c.1190C>G p.S397* Substitution - Nonsense 4:145150582-145150582 - TCGA-GV-A3JW-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - T2269 COSM4710570 c.3059A>C p.K1020T Substitution - Missense 4:145137716-145137716 - BD188T COSM3126734 c.978G>A p.A326A Substitution - coding silent 4:145150599-145150599 - PCSI_0090_Pa_X COSM3380827 c.774-6T>C p.? Unknown 4:145150911-145150911 - TCGA-EJ-7782-01 COSM3783785 c.3336G>A p.Q1112Q Substitution - coding silent 4:145137439-145137439 - TCGA-D9-A1JW-06 COSM3600652 c.998C>T p.P333L Substitution - Missense 4:145150876-145150876 - TCGA-EE-A2GM-06 COSM3600640 c.1667C>T p.P556L Substitution - Missense 4:145143381-145143381 - PD8615a COSM5789202 c.795G>A p.L265L Substitution - coding silent 4:145155582-145155582 - TCGA-FK-A3SH-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - SNU_17_S1 COSM4420231 c.1770A>C p.L590F Substitution - Missense 4:145142248-145142248 - TCGA-FJ-A3ZF-01 COSM3775588 c.3133C>T p.Q1045* Substitution - Nonsense 4:145137642-145137642 - TCGA-CA-6717-01 COSM3696353 c.1915A>C p.N639H Substitution - Missense 4:145139965-145139965 - TCGA-CM-4743-01 COSM4949053 c.1405G>A p.A469T Substitution - Missense 4:145146284-145146284 - Pat_60_B COSM5091532 c.458_460delCTG p.A153delA Deletion - In frame 4:145155971-145155973 - TCGA-HT-7695-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - BD72T COSM5512072 c.1736C>A p.P579Q Substitution - Missense 4:145142282-145142282 - TCGA-GC-A3RC-01 COSM3775590 c.1124C>G p.S375* Substitution - Nonsense 4:145150648-145150648 - pfg008T COSM1642418 c.2783T>C p.V928A Substitution - Missense 4:145137992-145137992 - TCGA-BR-6452-01 COSM4122543 c.2706T>C p.D902D Substitution - coding silent 4:145138069-145138069 - TCGA-BR-6452-01 COSM4122550 c.1250C>A p.A417D Substitution - Missense 4:145144412-145144412 - SNU_17_S1 COSM4420230 c.1575A>C p.L525F Substitution - Missense 4:145142248-145142248 - sysucc-311T COSM5466064 c.231G>T p.E77D Substitution - Missense 4:145174673-145174673 - TCGA-19-5954-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-FK-A3SB-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-EE-A2GM-06 COSM3600639 c.1472C>T p.P491L Substitution - Missense 4:145143381-145143381 - I2L-P24Tb-Tumor-Organoid COSM5356043 c.1699G>A p.V567M Substitution - Missense 4:145142319-145142319 - RG01 COSM3728216 c.1421C>G p.S474C Substitution - Missense 4:145146268-145146268 - TCGA-AP-A0LM-01 COSM1051723 c.2493T>C p.N831N Substitution - coding silent 4:145138087-145138087 - 522_T COSM3946045 c.157A>G p.I53V Substitution - Missense 4:145164216-145164216 - TCGA-BJ-A28X-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-AA-3510-01 COSM4710568 c.3266G>A p.R1089Q Substitution - Missense 4:145137509-145137509 - TCGA-AP-A0LM-01 COSM1051747 c.786G>T p.K262N Substitution - Missense 4:145150893-145150893 - TCGA-AX-A0J1-01 COSM4867823 c.2794C>T p.P932S Substitution - Missense 4:145137981-145137981 - BD72T COSM5512071 c.1541C>A p.P514Q Substitution - Missense 4:145142282-145142282 - TCGA-DK-A1AD-01 COSM1309778 c.1138G>A p.E380K Substitution - Missense 4:145146356-145146356 - TCGA-06-0216-01 COSM2150938 c.660G>A p.V220V Substitution - coding silent 4:145155966-145155966 - NPC015D COSM4420231 c.1770A>C p.L590F Substitution - Missense 4:145142248-145142248 - TCGA-DK-A3WW-01 COSM3775591 c.493G>A p.E165K Substitution - Missense 4:145155938-145155938 - 2492720 COSM5723741 c.1150G>T p.E384* Substitution - Nonsense 4:145146344-145146344 - PT14_1 COSM5943239 c.809-6delT p.? Unknown 4:145155481-145155481 - TCGA-HU-A4GQ-01 COSM4122538 c.2649G>A p.T883T Substitution - coding silent 4:145137931-145137931 - TCGA-GC-A3RC-01 COSM3775589 c.929C>G p.S310* Substitution - Nonsense 4:145150648-145150648 - TCGA-AH-6544-01 COSM4946271 c.1002A>C p.P334P Substitution - coding silent 4:145150872-145150872 - TCGA-EL-A3CN-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - 2290930 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - Pat_66_A COSM5865824 c.1538C>T p.S513F Substitution - Missense 4:145142285-145142285 - 52 COSM5734702 c.1232C>A p.S411* Substitution - Nonsense 4:145144430-145144430 - TCGA-FC-7708-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-AP-A056-01 COSM1051757 c.59G>A p.G20E Substitution - Missense 4:145171710-145171710 - TCGA-FS-A1ZK-06 COSM3600643 c.1115C>T p.S372F Substitution - Missense 4:145146379-145146379 - SNU-C4 COSM4653770 c.1787C>T p.A596V Substitution - Missense 4:145142231-145142231 - 2492710 COSM5718362 c.1924G>T p.V642L Substitution - Missense 4:145139956-145139956 - TCGA-CD-A4MG-01 COSM4122541 c.2830C>T p.R944* Substitution - Nonsense 4:145137945-145137945 - TCGA-JW-A5VL-01 COSM4847624 c.1450C>T p.Q484* Substitution - Nonsense 4:145144407-145144407 - TCGA-BR-8680-01 COSM4122544 c.2470G>A p.E824K Substitution - Missense 4:145138110-145138110 - 8035328 COSM1723213 c.2961C>T p.S987S Substitution - coding silent 4:145137814-145137814 - PTC-10C COSM4158841 c.2944T>G p.Y982D Substitution - Missense 4:145137636-145137636 - TCGA-EE-A20C-06 COSM3600645 c.995C>G p.S332* Substitution - Nonsense 4:145150582-145150582 - TCGA-AP-A056-01 COSM1051749 c.760G>T p.E254* Substitution - Nonsense 4:145152554-145152554 - TCGA-EE-A20H-06 COSM3600650 c.1046C>T p.S349F Substitution - Missense 4:145150828-145150828 - TCGA-BS-A0UF-01 COSM1051753 c.494A>C p.E165A Substitution - Missense 4:145155937-145155937 - TCGA-EE-A2GD-06 COSM3600638 c.1999C>T p.P667S Substitution - Missense 4:145141463-145141463 - B85-2 COSM1753559 c.1304G>A p.R435K Substitution - Missense 4:145144358-145144358 - TCGA-FE-A3PD-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-D8-A1JA-01 COSM3825282 c.2456C>T p.S819F Substitution - Missense 4:145138124-145138124 - UM-SCC-17B COSM4598487 c.1688C>T p.S563L Substitution - Missense 4:145141579-145141579 - CHC1746T COSM4787909 c.1112T>C p.I371T Substitution - Missense 4:145150660-145150660 - TCGA-G4-6628-01 COSM4782791 c.3329G>T p.R1110M Substitution - Missense 4:145137446-145137446 - TCGA-B5-A11N-01 COSM4864082 c.2972A>C p.K991T Substitution - Missense 4:145137803-145137803 - TCGA-AX-A0J0-01 COSM1051715 c.2773G>T p.E925* Substitution - Nonsense 4:145137807-145137807 - 2290930 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-CM-4743-01 COSM1427363 c.1210G>A p.A404T Substitution - Missense 4:145146284-145146284 - TCGA-AP-A059-01 COSM3126731 c.1277G>T p.R426I Substitution - Missense 4:145146412-145146412 - ESO-0950 COSM1260729 c.613G>A p.A205T Substitution - Missense 4:145155569-145155569 - TCGA-BS-A0TC-01 COSM4871287 c.1114A>C p.K372Q Substitution - Missense 4:145150658-145150658 - TCGA-D1-A17Q-01 COSM4865129 c.2030G>A p.R677Q Substitution - Missense 4:145141432-145141432 - 8035328 COSM1723212 c.2766C>T p.S922S Substitution - coding silent 4:145137814-145137814 - TCGA-AX-A0J0-01 COSM1051725 c.2470G>T p.E824* Substitution - Nonsense 4:145138110-145138110 - TCGA-AP-A0LM-01 COSM1051751 c.747A>C p.P249P Substitution - coding silent 4:145152567-145152567 - TCGA-HU-A4GN-01 COSM4122549 c.1614T>C p.D538D Substitution - coding silent 4:145143434-145143434 - TCGA-B5-A0K9-01 COSM1051733 c.1467G>A p.E489E Substitution - coding silent 4:145143386-145143386 - EW8 COSM3126752 c.496C>A p.Q166K Substitution - Missense 4:145155686-145155686 - TCGA-06-0216 COSM2150938 c.660G>A p.V220V Substitution - coding silent 4:145155966-145155966 - 2_RESISTANT COSM1723213 c.2961C>T p.S987S Substitution - coding silent 4:145137814-145137814 - TCGA-F5-6814-01 COSM3428204 c.1408-1G>T p.? Unknown 4:145143446-145143446 - S02209 COSM5675350 c.481T>G p.L161V Substitution - Missense 4:145155950-145155950 - TCGA-D9-A1JW-06 COSM3600651 c.803C>T p.P268L Substitution - Missense 4:145150876-145150876 - PCSI_0090_Pa_X COSM3380828 c.969-6T>C p.? Unknown 4:145150911-145150911 - CSCC-29-T COSM4473858 c.2074C>T p.L692L Substitution - coding silent 4:145141388-145141388 - TCGA-EB-A4IS-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - T3090 COSM4710574 c.2167C>A p.P723T Substitution - Missense 4:145138608-145138608 - CSCC-55-T COSM4512489 c.1099C>T p.P367S Substitution - Missense 4:145150673-145150673 - TCGA-BS-A0UF-01 COSM4875912 c.217C>T p.R73* Substitution - Nonsense 4:145174687-145174687 - TCGA-EE-A3JA-06 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - Pat_70_B COSM5091532 c.458_460delCTG p.A153delA Deletion - In frame 4:145155971-145155973 - CHC1746T COSM4787909 c.1112T>C p.I371T Substitution - Missense 4:145150660-145150660 - TCGA-AD-6895-01 COSM1427365 c.583G>T p.E195* Substitution - Nonsense 4:145155599-145155599 - TCGA-B5-A11N-01 COSM1051713 c.2777A>C p.K926T Substitution - Missense 4:145137803-145137803 - sysucc-311T COSM5466062 c.1632T>G p.V544V Substitution - coding silent 4:145143416-145143416 - TCGA-GF-A6C9-06 COSM4902559 c.1227C>T p.S409S Substitution - coding silent 4:145146267-145146267 - CSCC-30-T COSM4513026 c.1119C>T p.A373A Substitution - coding silent 4:145150653-145150653 - TCGA-AP-A0LM-01 COSM4873414 c.942A>C p.P314P Substitution - coding silent 4:145152567-145152567 - TCGA-AA-3510-01 COSM1427351 c.3071G>A p.R1024Q Substitution - Missense 4:145137509-145137509 - ESCC_99 COSM5637775 c.2704A>T p.I902F Substitution - Missense 4:145137876-145137876 - TCGA-EM-A22Q-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - TCGA-JW-A5VL-01 COSM4847623 c.1255C>T p.Q419* Substitution - Nonsense 4:145144407-145144407 - PT25 COSM5943239 c.809-6delT p.? Unknown 4:145155481-145155481 - TCGA-A8-A07E-01 COSM4815317 c.766T>C p.Y256H Substitution - Missense 4:145155611-145155611 - PCSI_0217_Pa_P_526 COSM4961820 c.177T>A p.S59S Substitution - coding silent 4:145174727-145174727 - 587304 COSM1218999 c.1676C>T p.T559I Substitution - Missense 4:145141591-145141591 - Pat_53_B COSM5091532 c.458_460delCTG p.A153delA Deletion - In frame 4:145155971-145155973 - TCGA-AA-A010-01 COSM283656 c.3076G>T p.V1026F Substitution - Missense 4:145137504-145137504 - C547 COSM4442509 c.1457G>A p.S486N Substitution - Missense 4:145144400-145144400 - TCGA-12-0670 COSM2153837 c.1686G>C p.K562N Substitution - Missense 4:145142332-145142332 - I2L-P24Ta-Tumor-Biopsy COSM5356053 c.684G>T p.R228S Substitution - Missense 4:145152630-145152630 - 2290930 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - 55 COSM5014458 c.553G>T p.V185L Substitution - Missense 4:145159579-145159579 - TCGA-GV-A3JW-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - sysucc-1028T COSM5469036 c.1481C>A p.S494* Substitution - Nonsense 4:145144376-145144376 - TCGA-HU-A4GQ-01 COSM4122539 c.2844G>A p.T948T Substitution - coding silent 4:145137931-145137931 - TCGA-B5-A0K9-01 COSM1051717 c.2714G>C p.R905T Substitution - Missense 4:145137866-145137866 - TCGA-56-5898-01 COSM732490 c.1478C>T p.P493L Substitution - Missense 4:145143375-145143375 - TCGA-GF-A6C9-06 COSM4902560 c.1422C>T p.S474S Substitution - coding silent 4:145146267-145146267 - CRC-02T COSM5455273 c.1534C>T p.R512* Substitution - Nonsense 4:145144323-145144323 - TCGA-GV-A3JW-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-GV-A3JZ-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-AZ-4315-01 COSM1427351 c.3071G>A p.R1024Q Substitution - Missense 4:145137509-145137509 - CHC197T COSM3669213 c.1870A>G p.T624A Substitution - Missense 4:145141592-145141592 - 661-06-01TD COSM5418929 c.3126C>A p.F1042L Substitution - Missense 4:145137649-145137649 - TCGA-HT-7688-01 COSM3783786 c.2841T>G p.V947V Substitution - coding silent 4:145137739-145137739 - YUROL COSM5400564 c.2722G>C p.E908Q Substitution - Missense 4:145137858-145137858 - 2492721 COSM5723741 c.1150G>T p.E384* Substitution - Nonsense 4:145146344-145146344 - TCGA-G4-6586-01 COSM4122537 c.2909G>C p.R970T Substitution - Missense 4:145137866-145137866 - TCGA-F5-6814-01 COSM3428205 c.1603-1G>T p.? Unknown 4:145143446-145143446 - TCGA-AN-A0AM-01 COSM447442 c.570C>G p.V190V Substitution - coding silent 4:145155612-145155612 - Pat_14_B COSM233031 c.1475C>T p.S492F Substitution - Missense 4:145143378-145143378 - TCGA-HT-7695-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - TCGA-EE-A2MI-06 COSM3600654 c.831C>T p.S277S Substitution - coding silent 4:145155453-145155453 - Pat_54_A COSM5129198 c.2917_2918delGA p.E973fs*5 Deletion - Frameshift 4:145137857-145137858 - TCGA-BR-8297-01 COSM4122552 c.1167A>C p.E389D Substitution - Missense 4:145146327-145146327 - TCGA-AZ-4315-01 COSM4710568 c.3266G>A p.R1089Q Substitution - Missense 4:145137509-145137509 - sysucc-311T COSM5466061 c.1437T>G p.V479V Substitution - coding silent 4:145143416-145143416 - TCGA-A5-A0G9-01 COSM1051727 c.2303G>A p.G768D Substitution - Missense 4:145138277-145138277 - Case5e COSM1717137 c.803A>G p.K268R Substitution - Missense 4:145155574-145155574 - TCGA-B0-5110-01 COSM4858103 c.1720C>T p.P574S Substitution - Missense 4:145142298-145142298 - Pat_65_A COSM5091533 c.653_655delCTG p.A218delA Deletion - In frame 4:145155971-145155973 - TCGA-G4-6586-01 COSM1051717 c.2714G>C p.R905T Substitution - Missense 4:145137866-145137866 - TCGA-B2-5633-01 COSM480917 c.2658T>C p.A886A Substitution - coding silent 4:145137922-145137922 - CRC-02T COSM5455272 c.1339C>T p.R447* Substitution - Nonsense 4:145144323-145144323 - CSCC-27-T COSM4513776 c.289C>T p.P97S Substitution - Missense 4:145171675-145171675 - TCGA-A6-6138-01 COSM4784214 c.2769C>T p.L923L Substitution - coding silent 4:145138006-145138006 - UM-SCC-17B COSM4598488 c.1883C>T p.S628L Substitution - Missense 4:145141579-145141579 - TCGA-EB-A44O-01 COSM3600648 c.1150C>T p.P384S Substitution - Missense 4:145150622-145150622 - T2269 COSM4710568 c.3266G>A p.R1089Q Substitution - Missense 4:145137509-145137509 - Case5h COSM1717137 c.803A>G p.K268R Substitution - Missense 4:145155574-145155574 - YUROL COSM5400565 c.2917G>C p.E973Q Substitution - Missense 4:145137858-145137858 - ESCC_99 COSM5637776 c.2899A>T p.I967F Substitution - Missense 4:145137876-145137876 - ESCC-148T COSM3940760 c.2482G>A p.E828K Substitution - Missense 4:145138293-145138293 - TCGA-32-2634-01 COSM3409072 c.1972C>T p.P658S Substitution - Missense 4:145138608-145138608 - CHC197T COSM3669212 c.1675A>G p.T559A Substitution - Missense 4:145141592-145141592 - CSCC-30-T COSM4513025 c.924C>T p.A308A Substitution - coding silent 4:145150653-145150653 - XHDG27 COSM4769149 c.1150G>A p.E384K Substitution - Missense 4:145146344-145146344 - T3090 COSM4710573 c.1972C>A p.P658T Substitution - Missense 4:145138608-145138608 - TCGA-AN-A046-01 COSM3825285 c.2502G>T p.K834N Substitution - Missense 4:145138273-145138273 - Pat_36_B COSM5865822 c.1619delG p.G540fs*14 Deletion - Frameshift 4:145142204-145142204 - TCGA-EJ-7789-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - CSCC-57-T COSM4467222 c.1477C>T p.P493S Substitution - Missense 4:145143376-145143376 - PT42 COSM5925130 c.811C>A p.Q271K Substitution - Missense 4:145155473-145155473 - TCGA-66-2763-01 COSM4859691 c.911A>T p.D304V Substitution - Missense 4:145152598-145152598 - TCGA-BR-8680-01 COSM4122558 c.1059A>C p.Q353H Substitution - Missense 4:145150815-145150815 - TCGA-06-0157-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - Case5f COSM1717137 c.803A>G p.K268R Substitution - Missense 4:145155574-145155574 - J46_T COSM3946044 c.1285G>C p.D429H Substitution - Missense 4:145146404-145146404 - TCGA-AN-A0AM-01 COSM4813570 c.765C>G p.V255V Substitution - coding silent 4:145155612-145155612 - PD8615a COSM5789201 c.600G>A p.L200L Substitution - coding silent 4:145155582-145155582 - TCGA-FC-7708-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-EB-A4IS-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-FU-A23L-01 COSM460682 c.2919A>T p.R973S Substitution - Missense 4:145137661-145137661 - TCGA-EB-A430-01 COSM3600655 c.329C>T p.S110F Substitution - Missense 4:145165163-145165163 - TCGA-BR-8680-01 COSM4122557 c.864A>C p.Q288H Substitution - Missense 4:145150815-145150815 - TCGA-E2-A15R-01 COSM447439 c.1864C>T p.Q622* Substitution - Nonsense 4:145141403-145141403 - PT14_1 COSM5943238 c.614-6delT p.? Unknown 4:145155481-145155481 - TCGA-FD-A3NA-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - 2290929 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - TCGA-EE-A29M-06 COSM3600642 c.1463C>T p.P488L Substitution - Missense 4:145144394-145144394 - TCGA-D8-A27E-01 COSM4814779 c.3025G>A p.A1009T Substitution - Missense 4:145137750-145137750 - Pat_60_B COSM5091533 c.653_655delCTG p.A218delA Deletion - In frame 4:145155971-145155973 - SNUH_G46_S1 COSM3126741 c.950T>C p.V317A Substitution - Missense 4:145152559-145152559 - 2492723 COSM5723742 c.1345G>T p.E449* Substitution - Nonsense 4:145146344-145146344 - TCGA-FC-7708-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - C0099T COSM4422523 c.137T>A p.L46H Substitution - Missense 4:145165160-145165160 - Pat_65_A COSM5865827 c.1319G>A p.R440Q Substitution - Missense 4:145144343-145144343 - TCGA-EJ-7789-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - RH18C COSM3126750 c.536C>T p.S179F Substitution - Missense 4:145155646-145155646 - TCGA-A8-A07E-01 COSM447441 c.571T>C p.Y191H Substitution - Missense 4:145155611-145155611 - 587376 COSM1051725 c.2470G>T p.E824* Substitution - Nonsense 4:145138110-145138110 - NPC015D COSM4420230 c.1575A>C p.L525F Substitution - Missense 4:145142248-145142248 - TCGA-HU-A4GN-01 COSM4122548 c.1419T>C p.D473D Substitution - coding silent 4:145143434-145143434 - TCGA-BS-A0UF-01 COSM4875452 c.689A>C p.E230A Substitution - Missense 4:145155937-145155937 - TCGA-FK-A3SH-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - B85-2-Tumor COSM1753560 c.1499G>A p.R500K Substitution - Missense 4:145144358-145144358 - TCGA-BR-8680-01 COSM4122559 c.845A>C p.K282T Substitution - Missense 4:145150834-145150834 - sysucc-1028T COSM5469035 c.1286C>A p.S429* Substitution - Nonsense 4:145144376-145144376 - Pat_54_A COSM1427359 c.2722_2723delGA p.E908fs*5 Deletion - Frameshift 4:145137857-145137858 - CSCC-27-T COSM4513775 c.94C>T p.P32S Substitution - Missense 4:145171675-145171675 - TCGA-FS-A1ZK-06 COSM3600644 c.1310C>T p.S437F Substitution - Missense 4:145146379-145146379 - TCGA-66-2785-01 COSM4861956 c.627C>G p.C209W Substitution - Missense 4:145159505-145159505 - TCGA-D8-A27E-01 COSM1485710 c.2830G>A p.A944T Substitution - Missense 4:145137750-145137750 - I2L-P24Ta-Tumor-Organoid COSM5356042 c.1504G>A p.V502M Substitution - Missense 4:145142319-145142319 - TCGA-CG-5721-01 COSM4122546 c.2264G>A p.G755E Substitution - Missense 4:145138316-145138316 - Hs-578-T COSM1671348 c.874-2A>G p.? Unknown 4:145152637-145152637 - TCGA-BQ-5889-01 COSM3993486 c.734G>T p.R245I Substitution - Missense 4:145155643-145155643 - TCGA-EM-A22Q-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - TCGA-AX-A0J0-01 COSM4867373 c.2665G>T p.E889* Substitution - Nonsense 4:145138110-145138110 - ESO-0292 COSM1241536 c.261G>A p.V87V Substitution - coding silent 4:145162680-145162680 - TCGA-BS-A0UF-01 COSM4875788 c.1383G>T p.E461D Substitution - Missense 4:145146306-145146306 - T2197 COSM4710567 c.3281G>A p.R1094Q Substitution - Missense 4:145137494-145137494 - SNUH_G46_S1 COSM3126740 c.755T>C p.V252A Substitution - Missense 4:145152559-145152559 - B85-2-Tumor COSM1753559 c.1304G>A p.R435K Substitution - Missense 4:145144358-145144358 - C008 COSM5523379 c.2822C>T p.S941F Substitution - Missense 4:145137953-145137953 - HCA7 COSM4630931 c.1270C>T p.R424C Substitution - Missense 4:145146419-145146419 - TCGA-BS-A0TC-01 COSM1051745 c.919A>C p.K307Q Substitution - Missense 4:145150658-145150658 - PT42 COSM5925129 c.616C>A p.Q206K Substitution - Missense 4:145155473-145155473 - CSCC-29-T COSM4473857 c.1879C>T p.L627L Substitution - coding silent 4:145141388-145141388 - CHC197T COSM3669212 c.1675A>G p.T559A Substitution - Missense 4:145141592-145141592 - HCA7 COSM4630930 c.1075C>T p.R359C Substitution - Missense 4:145146419-145146419 - 2492720 COSM5723742 c.1345G>T p.E449* Substitution - Nonsense 4:145146344-145146344 - TCGA-AA-A00N-01 COSM276568 c.1340G>A p.R447Q Substitution - Missense 4:145144322-145144322 - TCGA-HT-7688-01 COSM3783787 c.3036T>G p.V1012V Substitution - coding silent 4:145137739-145137739 - TCGA-FG-7634-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-AD-6895-01 COSM4783138 c.778G>T p.E260* Substitution - Nonsense 4:145155599-145155599 - C0099T COSM4422524 c.332T>A p.L111H Substitution - Missense 4:145165160-145165160 - TCGA-B5-A11U-01 COSM1051719 c.2600C>T p.P867L Substitution - Missense 4:145137980-145137980 - TCGA-HU-A4G8-01 COSM4122556 c.1108C>T p.P370S Substitution - Missense 4:145150664-145150664 - TCGA-AX-A0J0-01 COSM4867208 c.2968G>T p.E990* Substitution - Nonsense 4:145137807-145137807 - TCGA-BJ-A28X-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - Case5c COSM1717137 c.803A>G p.K268R Substitution - Missense 4:145155574-145155574 - BD136T COSM5507537 c.302-7A>T p.? Unknown 4:145159642-145159642 - TCGA-BQ-5889-01 COSM3993485 c.539G>T p.R180I Substitution - Missense 4:145155643-145155643 - TCGA-BS-A0UF-01 COSM1051737 c.1188G>T p.E396D Substitution - Missense 4:145146306-145146306 - TCGA-BS-A0UJ-01 COSM4871393 c.1179T>C p.S393S Substitution - coding silent 4:145150593-145150593 - I2L-P24Tb-Tumor-Biopsy COSM5356042 c.1504G>A p.V502M Substitution - Missense 4:145142319-145142319 - CSCC-17-T COSM4471668 c.1733C>T p.S578L Substitution - Missense 4:145141534-145141534 - I2L-P24Ta-Tumor-Organoid COSM5356054 c.879G>T p.R293S Substitution - Missense 4:145152630-145152630 - 2290930 COSM1723212 c.2766C>T p.S922S Substitution - coding silent 4:145137814-145137814 - TCGA-D1-A16F-01 COSM4870777 c.2363C>T p.P788L Substitution - Missense 4:145138412-145138412 - TCGA-EJ-7789-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-AN-A046-01 COSM3825284 c.2307G>T p.K769N Substitution - Missense 4:145138273-145138273 - OSCC-GB_00670111 COSM4883881 c.1663C>A p.Q555K Substitution - Missense 4:145141604-145141604 - RMS66_ COSM4988111 c.1508G>T p.S503I Substitution - Missense 4:145144349-145144349 - TCGA-A6-6138-01 COSM1427360 c.2574C>T p.L858L Substitution - coding silent 4:145138006-145138006 - TCGA-BR-8680-01 COSM4122545 c.2665G>A p.E889K Substitution - Missense 4:145138110-145138110 - TCGA-BR-6452-01 COSM4122551 c.1445C>A p.A482D Substitution - Missense 4:145144412-145144412 - TCGA-FE-A3PD-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - Hs578T COSM33544 c.679-2A>G p.? Unknown 4:145152637-145152637 - TCGA-06-0216 COSM2150937 c.465G>A p.V155V Substitution - coding silent 4:145155966-145155966 - TCGA-EE-A20H-06 COSM3600649 c.851C>T p.S284F Substitution - Missense 4:145150828-145150828 - PD5956a COSM5772063 c.2722G>T p.E908* Substitution - Nonsense 4:145137858-145137858 - T2197 COSM4710566 c.3086G>A p.R1029Q Substitution - Missense 4:145137494-145137494 - LUAD-NYU315 COSM373667 c.134C>T p.S45F Substitution - Missense 4:145165163-145165163 - RG01 COSM3728215 c.1226C>G p.S409C Substitution - Missense 4:145146268-145146268 - TCGA-C5-A1BF-01 COSM4836750 c.2517G>A p.Q839Q Substitution - coding silent 4:145138258-145138258 - TCGA-AA-3715-01 COSM269804 c.1083A>T p.R361S Substitution - Missense 4:145146411-145146411 - TCGA-DK-A1A6-01 COSM4811127 c.1812T>C p.F604F Substitution - coding silent 4:145142206-145142206 - LIM1899 COSM4640581 c.970C>T p.H324Y Substitution - Missense 4:145150904-145150904 - CSCC-62-T COSM4477800 c.2185C>T p.L729L Substitution - coding silent 4:145138395-145138395 - TCGA-AP-A056-01 COSM4868839 c.254G>A p.G85E Substitution - Missense 4:145171710-145171710 - TCGA-DK-A3WW-01 COSM3775592 c.688G>A p.E230K Substitution - Missense 4:145155938-145155938 - LUAD-E00897 COSM364640 c.3086G>T p.R1029L Substitution - Missense 4:145137494-145137494 - TCGA-12-0670 COSM2153836 c.1491G>C p.K497N Substitution - Missense 4:145142332-145142332 - Pat_65_A COSM5865828 c.1514G>A p.R505Q Substitution - Missense 4:145144343-145144343 - TCGA-EE-A2GD-06 COSM3600637 c.1804C>T p.P602S Substitution - Missense 4:145141463-145141463 - 234 COSM3730918 c.454G>A p.V152M Substitution - Missense 4:145162682-145162682 - TCGA-FU-A23L-01 COSM4854794 c.3114A>T p.R1038S Substitution - Missense 4:145137661-145137661 - T3091 COSM4710572 c.2789G>A p.S930N Substitution - Missense 4:145137986-145137986 - I2L-P24Ta-Tumor-Organoid COSM5356043 c.1699G>A p.V567M Substitution - Missense 4:145142319-145142319 - BD225T COSM5508684 c.2029C>A p.R677R Substitution - coding silent 4:145141433-145141433 - TCGA-E2-A15R-01 COSM4815979 c.2059C>T p.Q687* Substitution - Nonsense 4:145141403-145141403 - TCGA-EB-A430-01 COSM373667 c.134C>T p.S45F Substitution - Missense 4:145165163-145165163 - Pat_66_A COSM5865825 c.1733C>T p.S578F Substitution - Missense 4:145142285-145142285 - CHC909T COSM4806311 c.2758A>G p.I920V Substitution - Missense 4:145137822-145137822 - I2L-P24Ta-Tumor-Organoid COSM5356053 c.684G>T p.R228S Substitution - Missense 4:145152630-145152630 - Case5a COSM1717137 c.803A>G p.K268R Substitution - Missense 4:145155574-145155574 - PTC-10C COSM4158842 c.3139T>G p.Y1047D Substitution - Missense 4:145137636-145137636 - T2269 COSM4710569 c.2864A>C p.K955T Substitution - Missense 4:145137716-145137716 - KM12 COSM3126704 c.1527C>T p.P509P Substitution - coding silent 4:145142296-145142296 - KM12 COSM3126705 c.1722C>T p.P574P Substitution - coding silent 4:145142296-145142296 - HN_62469 COSM125087 c.196A>G p.T66A Substitution - Missense 4:145164177-145164177 - TCGA-FK-A3SB-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - pfg008T COSM1642417 c.2588T>C p.V863A Substitution - Missense 4:145137992-145137992 - TCGA-A8-A09Z-01 COSM3825286 c.161T>C p.V54A Substitution - Missense 4:145174743-145174743 - TCGA-DU-7306-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - OSCC-GB_01060111 COSM4883057 c.1232C>T p.S411L Substitution - Missense 4:145144430-145144430 - TCGA-DU-7306-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-DU-8158-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - I2L-P7-Tumor-Organoid COSM4710567 c.3281G>A p.R1094Q Substitution - Missense 4:145137494-145137494 - HCC146T COSM5824616 c.3085C>T p.R1029* Substitution - Nonsense 4:145137495-145137495 - TCGA-BR-4184-01 COSM4122554 c.1174T>C p.F392L Substitution - Missense 4:145150598-145150598 - LAU165 COSM233031 c.1475C>T p.S492F Substitution - Missense 4:145143378-145143378 - TCGA-FK-A3SH-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - TCGA-BS-A0UJ-01 COSM1051741 c.984T>C p.S328S Substitution - coding silent 4:145150593-145150593 - CHC909T COSM4806312 c.2953A>G p.I985V Substitution - Missense 4:145137822-145137822 - TCGA-FC-7708-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - ESCC-148T COSM3940759 c.2287G>A p.E763K Substitution - Missense 4:145138293-145138293 - S02209 COSM5675351 c.676T>G p.L226V Substitution - Missense 4:145155950-145155950 - CHC1746T COSM4787908 c.917T>C p.I306T Substitution - Missense 4:145150660-145150660 - TCGA-HU-A4GU-01 COSM1051717 c.2714G>C p.R905T Substitution - Missense 4:145137866-145137866 - sysucc-311T COSM3428204 c.1408-1G>T p.? Unknown 4:145143446-145143446 - TCGA-EB-A44O-01 COSM3600647 c.955C>T p.P319S Substitution - Missense 4:145150622-145150622 - V-PH-04T COSM4770298 c.442C>T p.H148Y Substitution - Missense 4:145162694-145162694 - TCGA-B5-A0K9-01 COSM4869829 c.1662G>A p.E554E Substitution - coding silent 4:145143386-145143386 - ESO-081 COSM1243475 c.1563G>A p.A521A Substitution - coding silent 4:145142260-145142260 - TCGA-DJ-A3UX-01 COSM1309775 c.2691T>C p.H897H Substitution - coding silent 4:145137889-145137889 - S02249 COSM5680157 c.2231C>G p.S744C Substitution - Missense 4:145138349-145138349 - sysucc-311T COSM3428205 c.1603-1G>T p.? Unknown 4:145143446-145143446 - TCGA-HC-7230-01 COSM1309774 c.2726C>T p.T909I Substitution - Missense 4:145137854-145137854 - ESCC_113 COSM5639610 c.909C>A p.S303R Substitution - Missense 4:145150668-145150668 - HCC146T COSM5824617 c.3280C>T p.R1094* Substitution - Nonsense 4:145137495-145137495 - TCGA-06-0157-01 COSM3748254 c.2886T>C p.H962H Substitution - coding silent 4:145137889-145137889 - 2492722 COSM5723742 c.1345G>T p.E449* Substitution - Nonsense 4:145146344-145146344 - HN_62921 COSM128734 c.1912_1914delTTC p.F638delF Deletion - In frame 4:145139966-145139968 - CSCC-11-T COSM4477363 c.2146C>T p.P716S Substitution - Missense 4:145138434-145138434 - PD5956a COSM5772064 c.2917G>T p.E973* Substitution - Nonsense 4:145137858-145137858 - PT44 COSM5926475 c.2782G>A p.E928K Substitution - Missense 4:145137798-145137798 - CSCC-62-T COSM4477801 c.2380C>T p.L794L Substitution - coding silent 4:145138395-145138395 - TCGA-DU-8158-01 COSM3126669 c.2921C>T p.T974I Substitution - Missense 4:145137854-145137854 - CSCC-17-T COSM4471669 c.1928C>T p.S643L Substitution - Missense 4:145141534-145141534 - CHC909T COSM4806312 c.2953A>G p.I985V Substitution - Missense 4:145137822-145137822 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.270851 4q31.21 611744

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - AAAA IntronicInsertion . c.1065-62_1065-59dupTTTT 4 146067640 CM A C Missense p.S974A c.2920T>G 4 146058812 OV A - Frameshift p.W199Gfs*2 c.595delT 4 146076739 RCCC A G IntronicSNV . c.1351+14T>C 4 146065449 STAD A G Missense p.V863A c.2588T>C 4 146059144 STAD A G Missense p.Y191H c.571T>C 4 146076763 BRCA A G Synonymous p.F539F c.1617T>C 4 146063358 BLCA A G Synonymous p.H897H c.2691T>C 4 146059041 BLCA A G Synonymous p.H897H c.2691T>C 4 146059041 CM A G Synonymous p.H897H c.2691T>C 4 146059041 GBM A G Synonymous p.H897H c.2691T>C 4 146059041 LGG A G Synonymous p.H897H c.2691T>C 4 146059041 THCA A T IntronicSNV . c.99+439T>A 4 146092383 HC CAG - InFrameDeletion p.A153delA c.458_460delCTG 4 146077123 BLCA CAG - InFrameDeletion p.A153delA c.458_460delCTG 4 146077123 LGG CAG - InFrameDeletion p.A153delA c.458_460delCTG 4 146077123 PRAD CAG - InFrameDeletion p.A153delA c.458_460delCTG 4 146077123 THCA C A Missense p.G376C c.1126G>T 4 146067520 LUAD C A Missense p.M98I c.294G>T 4 146083799 STAD C A Missense p.Q33H c.99G>T 4 146092822 OV C A Missense p.Q976H c.2928G>T 4 146058804 PRAD C A Missense p.R11I c.32G>T 4 146095829 SCLC C A Missense p.V1002L c.3004G>T 4 146058728 OV C - Frameshift p.T349Hfs*6 c.1044delG 4 146071685 HNSC C T 3-UTRSNV . c.3147+1682G>A 4 146056903 MB C T Missense p.A205T c.613G>A 4 146076721 ESCA C T Missense p.A944T c.2830G>A 4 146058902 BRCA C T Missense p.E380K c.1138G>A 4 146067508 BLCA C T Missense p.G804R c.2410G>A 4 146059322 CM C T Missense p.R11K c.32G>A 4 146095829 CM C T Missense p.R879Q c.2636G>A 4 146059096 LUAD C T Nonsense p.W797* c.2390G>A 4 146059342 CM C T Synonymous p.A494A c.1482G>A 4 146064523 BRCA C T Synonymous p.E489E c.1467G>A 4 146064538 UCEC C T Synonymous p.L659L c.1977G>A 4 146059755 CM C T Synonymous p.L829L c.2487G>A 4 146059245 BRCA C T Synonymous p.P722P c.2166G>A 4 146059566 COREAD C T Synonymous p.V155V c.465G>A 4 146077118 GBM G A Missense p.A494V c.1481C>T 4 146064524 NB G A Missense p.H367Y c.1099C>T 4 146067547 BRCA G A Missense p.P268L c.803C>T 4 146072028 CM G A Missense p.P32L c.95C>T 4 146092826 CM G A Missense p.P423L c.1268C>T 4 146065546 CM G A Missense p.P491L c.1472C>T 4 146064533 CM G A Missense p.P493L c.1478C>T 4 146064527 LUSC G A Missense p.P509S c.1525C>T 4 146063450 RCCC G A Missense p.P602S c.1804C>T 4 146062615 CM G A Missense p.P658S c.1972C>T 4 146059760 GBM G A Missense p.P723L c.2168C>T 4 146059564 UCEC G A Missense p.P867L c.2600C>T 4 146059132 UCEC G A Missense p.R348W c.1042C>T 4 146071687 LUAD G A Missense p.S284F c.851C>T 4 146071980 CM G A Missense p.S372F c.1115C>T 4 146067531 CM G A Missense p.T909I c.2726C>T 4 146059006 BLCA G A Missense p.T909I c.2726C>T 4 146059006 GBM G A Missense p.T909I c.2726C>T 4 146059006 LGG G A Missense p.T909I c.2726C>T 4 146059006 PRAD G A Missense p.T909I c.2726C>T 4 146059006 THCA G A Nonsense p.Q241* c.721C>T 4 146073745 LUAD G A Nonsense p.Q622* c.1864C>T 4 146062555 BRCA G A Synonymous p.A709A c.2127C>T 4 146059605 MM G A Synonymous p.F290F c.870C>T 4 146071961 CM G A Synonymous p.S212S c.636C>T 4 146076605 CM G C Missense p.P160R c.479C>G 4 146077104 LUAD G C Missense p.R359G c.1075C>G 4 146067571 LUSC G C Nonsense p.S332* c.995C>G 4 146071734 CM G C Synonymous p.V190V c.570C>G 4 146076764 BRCA - G Frameshift p.A527Sfs*9 c.1577dupC 4 146063398 RCCC T A Missense p.D239V c.716A>T 4 146073750 LUSC T C Missense p.T66A c.196A>G 4 146085329 HNSC - T Frameshift p.T883Nfs*31 c.2647dupA 4 146059085 LUAD T G Missense p.K307Q c.919A>C 4 146071810 UCEC