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 | 155458437 | 155458437 | + | Splice_Site | SNP | C | C | A | TCGA-ZF-A9RM-01A-11D-A38G-08 | TCGA-ZF-A9RM-10A-01D-A38J-08 | g.chr4:155458437C>A | | c.e14+1 | |
BLCA | 4 | 155458505 | 155458505 | + | Missense_Mutation | SNP | G | G | C | TCGA-CF-A1HR-01A-11D-A13W-08 | TCGA-CF-A1HR-10A-01D-A13W-08 | g.chr4:155458505G>C | c.1418C>G | c.(1417-1419)tCt>tGt | p.S473C |
BLCA | 4 | 155459229 | 155459229 | + | Missense_Mutation | SNP | T | T | C | TCGA-CU-A72E-01A-12D-A339-08 | TCGA-CU-A72E-10A-01D-A339-08 | g.chr4:155459229T>C | c.1183A>G | c.(1183-1185)Ata>Gta | p.I395V |
BLCA | 4 | 155461192 | 155461192 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr4:155461192C>G | c.953G>C | c.(952-954)aGa>aCa | p.R318T |
BLCA | 4 | 155470071 | 155470071 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr4:155470071G>C | c.26C>G | c.(25-27)tCt>tGt | p.S9C |
BRCA | 4 | 155465643 | 155465643 | + | Missense_Mutation | SNP | G | G | T | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr4:155465643G>T | c.548C>A | c.(547-549)cCt>cAt | p.P183H |
BRCA | 4 | 155466998 | 155466998 | + | Missense_Mutation | SNP | G | G | A | TCGA-AO-A12E-01A-11D-A10M-09 | TCGA-AO-A12E-10A-01D-A10M-09 | g.chr4:155466998G>A | c.482C>T | c.(481-483)gCg>gTg | p.A161V |
CESC | 4 | 155461841 | 155461841 | + | Missense_Mutation | SNP | G | G | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr4:155461841G>A | c.844C>T | c.(844-846)Cgg>Tgg | p.R282W |
CESC | 4 | 155470015 | 155470015 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VJ-01A-11D-A28B-09 | TCGA-JW-A5VJ-10A-01D-A28E-09 | g.chr4:155470015C>T | c.82G>A | c.(82-84)Gat>Aat | p.D28N |
CHOL | 4 | 155463385 | 155463385 | + | Missense_Mutation | SNP | G | G | A | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr4:155463385G>A | c.641C>T | c.(640-642)cCt>cTt | p.P214L |
COAD | 4 | 155461791 | 155461791 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:155461791C>T | c.894G>A | c.(892-894)ccG>ccA | p.P298P |
COAD | 4 | 155465613 | 155465613 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr4:155465613G>A | c.578C>T | c.(577-579)cCg>cTg | p.P193L |
COAD | 4 | 155465648 | 155465648 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:155465648delT | c.543delA | c.(541-543)aaafs | p.K181fs |
COAD | 4 | 155468976 | 155468976 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:155468976C>T | c.146G>A | c.(145-147)cGt>cAt | p.R49H |
COAD | 4 | 155468977 | 155468977 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:155468977G>A | c.145C>T | c.(145-147)Cgt>Tgt | p.R49C |
COADREAD | 4 | 155457840 | 155457840 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155457840A>C | c.1542T>G | c.(1540-1542)ttT>ttG | p.F514L |
COADREAD | 4 | 155459228 | 155459228 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155459228A>G | c.1184T>C | c.(1183-1185)aTa>aCa | p.I395T |
COADREAD | 4 | 155461791 | 155461791 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:155461791C>T | c.894G>A | c.(892-894)ccG>ccA | p.P298P |
COADREAD | 4 | 155461948 | 155461948 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155461948C>T | c.826G>A | c.(826-828)Gaa>Aaa | p.E276K |
COADREAD | 4 | 155465613 | 155465613 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr4:155465613G>A | c.578C>T | c.(577-579)cCg>cTg | p.P193L |
COADREAD | 4 | 155465648 | 155465648 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:155465648delT | c.543delA | c.(541-543)aaafs | p.K181fs |
COADREAD | 4 | 155468976 | 155468976 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:155468976C>T | c.146G>A | c.(145-147)cGt>cAt | p.R49H |
COADREAD | 4 | 155468977 | 155468977 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:155468977G>A | c.145C>T | c.(145-147)Cgt>Tgt | p.R49C |
ESCA | 4 | 155458497 | 155458497 | + | Silent | SNP | G | G | T | TCGA-V5-AASW-01A-11D-A403-09 | TCGA-V5-AASW-10A-01D-A403-09 | g.chr4:155458497G>T | c.1426C>A | c.(1426-1428)Cga>Aga | p.R476R |
ESCA | 4 | 155460362 | 155460362 | + | Missense_Mutation | SNP | C | C | A | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr4:155460362C>A | c.1046G>T | c.(1045-1047)aGc>aTc | p.S349I |
GBMLGG | 4 | 155459182 | 155459182 | + | Silent | SNP | G | G | A | TCGA-HT-7680-01A-11D-2253-08 | TCGA-HT-7680-10A-01D-2253-08 | g.chr4:155459182G>A | c.1230C>T | c.(1228-1230)tcC>tcT | p.S410S |
GBMLGG | 4 | 155463420 | 155463420 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:155463420C>T | c.606G>A | c.(604-606)ggG>ggA | p.G202G |
GBMLGG | 4 | 155468979 | 155468979 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:155468979A>C | c.143T>G | c.(142-144)cTt>cGt | p.L48R |
HNSC | 4 | 155457852 | 155457852 | + | Missense_Mutation | SNP | C | C | G | TCGA-CQ-7071-01A-12D-A30E-08 | TCGA-CQ-7071-10A-01D-A30H-08 | g.chr4:155457852C>G | c.1530G>C | c.(1528-1530)aaG>aaC | p.K510N |
HNSC | 4 | 155458554 | 155458554 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr4:155458554C>A | c.1369G>T | c.(1369-1371)Ggg>Tgg | p.G457W |
HNSC | 4 | 155459166 | 155459166 | + | Missense_Mutation | SNP | T | T | C | TCGA-CQ-5332-01A-01D-1683-08 | TCGA-CQ-5332-10A-01D-1683-08 | g.chr4:155459166T>C | c.1246A>G | c.(1246-1248)Att>Gtt | p.I416V |
HNSC | 4 | 155461982 | 155461982 | + | Missense_Mutation | SNP | A | A | C | TCGA-CN-A63T-01A-11D-A28R-08 | TCGA-CN-A63T-10A-01D-A28U-08 | g.chr4:155461982A>C | c.792T>G | c.(790-792)tgT>tgG | p.C264W |
KIPAN | 4 | 155465648 | 155465648 | + | Silent | SNP | T | T | C | TCGA-A4-7584-01A-11D-2136-08 | TCGA-A4-7584-10A-01D-2136-08 | g.chr4:155465648T>C | c.543A>G | c.(541-543)aaA>aaG | p.K181K |
KIPAN | 4 | 155470082 | 155470082 | + | Silent | SNP | T | T | C | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr4:155470082T>C | c.15A>G | c.(13-15)gtA>gtG | p.V5V |
KIRP | 4 | 155465648 | 155465648 | + | Silent | SNP | T | T | C | TCGA-A4-7584-01A-11D-2136-08 | TCGA-A4-7584-10A-01D-2136-08 | g.chr4:155465648T>C | c.543A>G | c.(541-543)aaA>aaG | p.K181K |
KIRP | 4 | 155470082 | 155470082 | + | Silent | SNP | T | T | C | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr4:155470082T>C | c.15A>G | c.(13-15)gtA>gtG | p.V5V |
LAML | 4 | 155458482 | 155458482 | + | Missense_Mutation | SNP | C | C | T | TCGA-AB-2905-03A-01D-0739-09 | TCGA-AB-2905-11A-01D-0739-09 | g.chr4:155458482C>T | c.1441G>A | c.(1441-1443)Gaa>Aaa | p.E481K |
LGG | 4 | 155459182 | 155459182 | + | Silent | SNP | G | G | A | TCGA-HT-7680-01A-11D-2253-08 | TCGA-HT-7680-10A-01D-2253-08 | g.chr4:155459182G>A | c.1230C>T | c.(1228-1230)tcC>tcT | p.S410S |
LGG | 4 | 155463420 | 155463420 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:155463420C>T | c.606G>A | c.(604-606)ggG>ggA | p.G202G |
LGG | 4 | 155468979 | 155468979 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:155468979A>C | c.143T>G | c.(142-144)cTt>cGt | p.L48R |
LIHC | 4 | 155457860 | 155457860 | + | Missense_Mutation | SNP | T | T | G | TCGA-G3-AAV1-01A-11D-A382-10 | TCGA-G3-AAV1-10A-01D-A385-10 | g.chr4:155457860T>G | c.1522A>C | c.(1522-1524)Att>Ctt | p.I508L |
LIHC | 4 | 155460255 | 155460255 | + | Splice_Site | SNP | A | A | G | TCGA-G3-AAV4-01A-11D-A382-10 | TCGA-G3-AAV4-10A-01D-A385-10 | g.chr4:155460255A>G | | c.e12+1 | |
LIHC | 4 | 155460301 | 155460301 | + | Silent | SNP | T | T | C | TCGA-G3-AAV1-01A-11D-A382-10 | TCGA-G3-AAV1-10A-01D-A385-10 | g.chr4:155460301T>C | c.1107A>G | c.(1105-1107)acA>acG | p.T369T |
LIHC | 4 | 155462030 | 155462030 | + | Silent | SNP | A | A | G | TCGA-DD-AAD1-01A-11D-A40R-10 | TCGA-DD-AAD1-10A-01D-A40U-10 | g.chr4:155462030A>G | c.744T>C | c.(742-744)acT>acC | p.T248T |
LUAD | 4 | 155458507 | 155458507 | + | Silent | SNP | C | C | T | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr4:155458507C>T | c.1416G>A | c.(1414-1416)caG>caA | p.Q472Q |
LUAD | 4 | 155459138 | 155459138 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8359-01A-11D-2323-08 | TCGA-86-8359-10A-01D-2323-08 | g.chr4:155459138C>A | c.1274G>T | c.(1273-1275)gGa>gTa | p.G425V |
LUAD | 4 | 155465648 | 155465648 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-55-5899-01A-11D-1625-08 | TCGA-55-5899-10A-01D-1625-08 | g.chr4:155465648delT | c.543delA | c.(541-543)aaafs | p.K181fs |
LUAD | 4 | 155468953 | 155468953 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4396-01A-21D-1855-08 | TCGA-05-4396-10A-01D-1855-08 | g.chr4:155468953G>T | c.169C>A | c.(169-171)Cat>Aat | p.H57N |
LUSC | 4 | 155458514 | 155458514 | + | Missense_Mutation | SNP | A | A | G | TCGA-18-3415-01A-01D-0983-08 | TCGA-18-3415-11A-01D-0983-08 | g.chr4:155458514A>G | c.1409T>C | c.(1408-1410)tTt>tCt | p.F470S |
LUSC | 4 | 155459240 | 155459240 | + | Missense_Mutation | SNP | G | G | C | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr4:155459240G>C | c.1172C>G | c.(1171-1173)tCt>tGt | p.S391C |
LUSC | 4 | 155460272 | 155460272 | + | Missense_Mutation | SNP | A | A | G | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr4:155460272A>G | c.1136T>C | c.(1135-1137)gTt>gCt | p.V379A |
LUSC | 4 | 155461791 | 155461791 | + | Silent | SNP | C | C | A | TCGA-21-1077-01A-01D-1521-08 | TCGA-21-1077-11A-01D-1521-08 | g.chr4:155461791C>A | c.894G>T | c.(892-894)ccG>ccT | p.P298P |
LUSC | 4 | 155467044 | 155467044 | + | Missense_Mutation | SNP | T | T | C | TCGA-43-6143-01A-11D-1817-08 | TCGA-43-6143-11A-01D-1817-08 | g.chr4:155467044T>C | c.436A>G | c.(436-438)Agt>Ggt | p.S146G |
LUSC | 4 | 155467273 | 155467273 | + | Splice_Site | SNP | A | A | T | TCGA-39-5024-01A-21D-1817-08 | TCGA-39-5024-11A-01D-1817-08 | g.chr4:155467273A>T | | c.e5+1 | |
PAAD | 4 | 155458483 | 155458483 | + | Silent | SNP | A | A | C | TCGA-HZ-A8P0-01A-11D-A36O-08 | TCGA-HZ-A8P0-10A-01D-A367-08 | g.chr4:155458483A>C | c.1440T>G | c.(1438-1440)gcT>gcG | p.A480A |
PAAD | 4 | 155465619 | 155465619 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr4:155465619T>C | c.572A>G | c.(571-573)cAc>cGc | p.H191R |
PRAD | 4 | 155467028 | 155467028 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZG-A9KY-01A-11D-A41K-08 | TCGA-ZG-A9KY-10A-01D-A41N-08 | g.chr4:155467028G>A | c.452C>T | c.(451-453)cCt>cTt | p.P151L |
READ | 4 | 155457840 | 155457840 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155457840A>C | c.1542T>G | c.(1540-1542)ttT>ttG | p.F514L |
READ | 4 | 155459228 | 155459228 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155459228A>G | c.1184T>C | c.(1183-1185)aTa>aCa | p.I395T |
READ | 4 | 155461948 | 155461948 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:155461948C>T | c.826G>A | c.(826-828)Gaa>Aaa | p.E276K |
SKCM | 4 | 155458438 | 155458438 | + | Splice_Site | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr4:155458438G>A | c.1485C>T | c.(1483-1485)gcC>gcT | p.A495A |
SKCM | 4 | 155460287 | 155460287 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr4:155460287G>A | c.1121C>T | c.(1120-1122)tCa>tTa | p.S374L |
SKCM | 4 | 155461135 | 155461135 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JK-06A-11D-A196-08 | TCGA-D3-A2JK-10A-01D-A198-08 | g.chr4:155461135C>T | c.1010G>A | c.(1009-1011)aGa>aAa | p.R337K |
SKCM | 4 | 155461949 | 155461949 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr4:155461949G>A | c.825C>T | c.(823-825)ctC>ctT | p.L275L |
SKCM | 4 | 155461993 | 155461993 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr4:155461993G>A | c.781C>T | c.(781-783)Ctg>Ttg | p.L261L |
SKCM | 4 | 155465644 | 155465644 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZF-06A-12D-A197-08 | TCGA-FS-A1ZF-10A-01D-A199-08 | g.chr4:155465644G>A | c.547C>T | c.(547-549)Cct>Tct | p.P183S |
SKCM | 4 | 155467365 | 155467365 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A29V-06A-12D-A197-08 | TCGA-EE-A29V-10A-01D-A199-08 | g.chr4:155467365C>T | c.314G>A | c.(313-315)gGg>gAg | p.G105E |
SKCM | 4 | 155469997 | 155469997 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr4:155469997G>A | c.100C>T | c.(100-102)Cct>Tct | p.P34S |