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 | 15 | 70346823 | 70346823 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A43X-01A-11D-A23U-08 | TCGA-FD-A43X-10A-01D-A23U-08 | g.chr15:70346823C>T | c.1789G>A | c.(1789-1791)Gat>Aat | p.D597N |
BLCA | 15 | 70346924 | 70346924 | + | Missense_Mutation | SNP | G | G | A | TCGA-C4-A0F1-01A-11D-A10S-08 | TCGA-C4-A0F1-10A-01D-A10S-08 | g.chr15:70346924G>A | c.1688C>T | c.(1687-1689)tCg>tTg | p.S563L |
BLCA | 15 | 70347433 | 70347433 | + | Silent | SNP | G | G | T | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr15:70347433G>T | c.1542C>A | c.(1540-1542)atC>atA | p.I514I |
BLCA | 15 | 70358355 | 70358355 | + | Missense_Mutation | SNP | C | C | G | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chr15:70358355C>G | c.575G>C | c.(574-576)aGa>aCa | p.R192T |
BLCA | 15 | 70358416 | 70358416 | + | Silent | SNP | G | G | A | TCGA-ZF-A9RM-01A-11D-A38G-08 | TCGA-ZF-A9RM-10A-01D-A38J-08 | g.chr15:70358416G>A | c.514C>T | c.(514-516)Ctg>Ttg | p.L172L |
BLCA | 15 | 70389121 | 70389121 | + | Missense_Mutation | SNP | C | C | G | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr15:70389121C>G | c.17G>C | c.(16-18)aGa>aCa | p.R6T |
BRCA | 15 | 70345629 | 70345629 | + | Missense_Mutation | SNP | G | G | T | TCGA-EW-A1J2-01A-21D-A13L-09 | TCGA-EW-A1J2-10A-01W-A14R-09 | g.chr15:70345629G>T | c.1920C>A | c.(1918-1920)aaC>aaA | p.N640K |
BRCA | 15 | 70345643 | 70345643 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr15:70345643C>T | c.1906G>A | c.(1906-1908)Ggg>Agg | p.G636R |
BRCA | 15 | 70346800 | 70346800 | + | Missense_Mutation | SNP | G | G | C | TCGA-BH-A0BZ-01A-31D-A12Q-09 | TCGA-BH-A0BZ-11A-61D-A12Q-09 | g.chr15:70346800G>C | c.1812C>G | c.(1810-1812)gaC>gaG | p.D604E |
BRCA | 15 | 70347454 | 70347454 | + | Silent | SNP | G | G | A | TCGA-B6-A1KI-01A-11D-A14K-09 | TCGA-B6-A1KI-10A-01W-A16I-09 | g.chr15:70347454G>A | c.1521C>T | c.(1519-1521)ggC>ggT | p.G507G |
BRCA | 15 | 70347638 | 70347638 | + | Splice_Site | SNP | C | C | G | TCGA-BH-A1F8-01A-11D-A13L-09 | TCGA-BH-A1F8-11B-21D-A188-09 | g.chr15:70347638C>G | | c.e15-1 | |
BRCA | 15 | 70350527 | 70350527 | + | Missense_Mutation | SNP | G | G | C | TCGA-C8-A134-01A-11D-A10Y-09 | TCGA-C8-A134-10A-01D-A110-09 | g.chr15:70350527G>C | c.1022C>G | c.(1021-1023)cCg>cGg | p.P341R |
BRCA | 15 | 70366914 | 70366916 | + | In_Frame_Del | DEL | GCG | GCG | - | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr15:70366914_70366916delGCG | c.328_330delCGC | c.(328-330)cgcdel | p.R110del |
COAD | 15 | 70344856 | 70344856 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70344856G>A | c.1991C>T | c.(1990-1992)tCg>tTg | p.S664L |
COAD | 15 | 70345575 | 70345575 | + | Silent | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr15:70345575G>A | c.1974C>T | c.(1972-1974)ttC>ttT | p.F658F |
COAD | 15 | 70347501 | 70347501 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr15:70347501C>T | c.1474G>A | c.(1474-1476)Gtg>Atg | p.V492M |
COAD | 15 | 70347531 | 70347531 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr15:70347531T>C | c.1444A>G | c.(1444-1446)Aca>Gca | p.T482A |
COAD | 15 | 70347546 | 70347546 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:70347546C>T | c.1429G>A | c.(1429-1431)Gcc>Acc | p.A477T |
COAD | 15 | 70347553 | 70347553 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr15:70347553C>T | c.1422G>A | c.(1420-1422)ccG>ccA | p.P474P |
COAD | 15 | 70349945 | 70349945 | + | Silent | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70349945G>A | c.1113C>T | c.(1111-1113)ttC>ttT | p.F371F |
COAD | 15 | 70351138 | 70351138 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:70351138C>T | c.782G>A | c.(781-783)cGg>cAg | p.R261Q |
COAD | 15 | 70352874 | 70352874 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70352874G>A | c.709C>T | c.(709-711)Cga>Tga | p.R237* |
COAD | 15 | 70356806 | 70356806 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70356806C>T | c.581G>A | c.(580-582)aGa>aAa | p.R194K |
COAD | 15 | 70358528 | 70358528 | + | Silent | SNP | G | G | A | TCGA-AA-3666-01A-02W-0900-09 | TCGA-AA-3666-10A-01W-0900-09 | g.chr15:70358528G>A | c.402C>T | c.(400-402)tcC>tcT | p.S134S |
COAD | 15 | 70358541 | 70358541 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr15:70358541G>A | c.389C>T | c.(388-390)gCg>gTg | p.A130V |
COAD | 15 | 70366913 | 70366913 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr15:70366913C>T | c.331G>A | c.(331-333)Gcc>Acc | p.A111T |
COAD | 15 | 70366913 | 70366913 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70366913C>T | c.331G>A | c.(331-333)Gcc>Acc | p.A111T |
COADREAD | 15 | 70344856 | 70344856 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70344856G>A | c.1991C>T | c.(1990-1992)tCg>tTg | p.S664L |
COADREAD | 15 | 70345575 | 70345575 | + | Silent | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr15:70345575G>A | c.1974C>T | c.(1972-1974)ttC>ttT | p.F658F |
COADREAD | 15 | 70345690 | 70345690 | + | Missense_Mutation | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:70345690C>T | c.1859G>A | c.(1858-1860)gGg>gAg | p.G620E |
COADREAD | 15 | 70347501 | 70347501 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr15:70347501C>T | c.1474G>A | c.(1474-1476)Gtg>Atg | p.V492M |
COADREAD | 15 | 70347531 | 70347531 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr15:70347531T>C | c.1444A>G | c.(1444-1446)Aca>Gca | p.T482A |
COADREAD | 15 | 70347546 | 70347546 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:70347546C>T | c.1429G>A | c.(1429-1431)Gcc>Acc | p.A477T |
COADREAD | 15 | 70347553 | 70347553 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr15:70347553C>T | c.1422G>A | c.(1420-1422)ccG>ccA | p.P474P |
COADREAD | 15 | 70349945 | 70349945 | + | Silent | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70349945G>A | c.1113C>T | c.(1111-1113)ttC>ttT | p.F371F |
COADREAD | 15 | 70351138 | 70351138 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:70351138C>T | c.782G>A | c.(781-783)cGg>cAg | p.R261Q |
COADREAD | 15 | 70352874 | 70352874 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70352874G>A | c.709C>T | c.(709-711)Cga>Tga | p.R237* |
COADREAD | 15 | 70356806 | 70356806 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70356806C>T | c.581G>A | c.(580-582)aGa>aAa | p.R194K |
COADREAD | 15 | 70358528 | 70358528 | + | Silent | SNP | G | G | A | TCGA-AA-3666-01A-02W-0900-09 | TCGA-AA-3666-10A-01W-0900-09 | g.chr15:70358528G>A | c.402C>T | c.(400-402)tcC>tcT | p.S134S |
COADREAD | 15 | 70358541 | 70358541 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr15:70358541G>A | c.389C>T | c.(388-390)gCg>gTg | p.A130V |
COADREAD | 15 | 70366913 | 70366913 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr15:70366913C>T | c.331G>A | c.(331-333)Gcc>Acc | p.A111T |
COADREAD | 15 | 70366913 | 70366913 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:70366913C>T | c.331G>A | c.(331-333)Gcc>Acc | p.A111T |
DLBC | 15 | 70347482 | 70347482 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6906-01A-11D-2210-10 | TCGA-G8-6906-14A-01D-2210-10 | g.chr15:70347482G>A | c.1493C>T | c.(1492-1494)aCg>aTg | p.T498M |
DLBC | 15 | 70351154 | 70351154 | + | Splice_Site | SNP | C | C | T | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr15:70351154C>T | c.766G>A | c.(766-768)Gac>Aac | p.D256N |
ESCA | 15 | 70343732 | 70343732 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-R6-A6Y2-01B-11D-A33E-09 | TCGA-R6-A6Y2-10A-01D-A33H-09 | g.chr15:70343732G>A | c.2209C>T | c.(2209-2211)Cag>Tag | p.Q737* |
GBM | 15 | 70347545 | 70347545 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr15:70347545G>A | c.1430C>T | c.(1429-1431)gCc>gTc | p.A477V |
GBMLGG | 15 | 70347545 | 70347545 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr15:70347545G>A | c.1430C>T | c.(1429-1431)gCc>gTc | p.A477V |
GBMLGG | 15 | 70347546 | 70347546 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:70347546C>T | c.1429G>A | c.(1429-1431)Gcc>Acc | p.A477T |
GBMLGG | 15 | 70347560 | 70347560 | + | Missense_Mutation | SNP | C | C | T | TCGA-P5-A731-01A-11D-A32B-08 | TCGA-P5-A731-10A-01D-A329-08 | g.chr15:70347560C>T | c.1415G>A | c.(1414-1416)gGc>gAc | p.G472D |
GBMLGG | 15 | 70350628 | 70350628 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:70350628G>A | c.921C>T | c.(919-921)aaC>aaT | p.N307N |
GBMLGG | 15 | 70366872 | 70366872 | + | Splice_Site | SNP | C | C | T | TCGA-CS-6670-01A-11D-1893-08 | TCGA-CS-6670-10A-01D-1893-08 | g.chr15:70366872C>T | c.372G>A | c.(370-372)ggG>ggA | p.G124G |
HNSC | 15 | 70350626 | 70350626 | + | Missense_Mutation | SNP | T | T | C | TCGA-UF-A7J9-01A-12D-A34J-08 | TCGA-UF-A7J9-10A-01D-A34M-08 | g.chr15:70350626T>C | c.923A>G | c.(922-924)gAc>gGc | p.D308G |
HNSC | 15 | 70351092 | 70351092 | + | Silent | SNP | G | G | A | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr15:70351092G>A | c.828C>T | c.(826-828)gcC>gcT | p.A276A |
HNSC | 15 | 70358436 | 70358436 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr15:70358436C>T | c.494G>A | c.(493-495)gGg>gAg | p.G165E |
HNSC | 15 | 70368499 | 70368499 | + | Splice_Site | SNP | T | T | C | TCGA-D6-A6EM-01A-21D-A31L-08 | TCGA-D6-A6EM-10A-01D-A31J-08 | g.chr15:70368499T>C | | c.e5-2 | |
KICH | 15 | 70386891 | 70386892 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KN-8437-01A-11D-2310-10 | TCGA-KN-8437-11A-01D-2311-10 | g.chr15:70386891_70386892insA | c.213_214insT | c.(211-216)ttgaacfs | p.N72fs |
KIPAN | 15 | 70351055 | 70351055 | + | Missense_Mutation | SNP | A | A | T | TCGA-B0-5703-01A-11D-1534-10 | TCGA-B0-5703-11A-01D-1534-10 | g.chr15:70351055A>T | c.865T>A | c.(865-867)Tcg>Acg | p.S289T |
KIPAN | 15 | 70368448 | 70368448 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-B8-4622-01A-02D-1553-08 | TCGA-B8-4622-11A-01D-1553-08 | g.chr15:70368448delA | c.284delT | c.(283-285)ttcfs | p.F95fs |
KIPAN | 15 | 70368460 | 70368460 | + | Missense_Mutation | SNP | T | T | A | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr15:70368460T>A | c.272A>T | c.(271-273)cAg>cTg | p.Q91L |
KIPAN | 15 | 70386891 | 70386892 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KN-8437-01A-11D-2310-10 | TCGA-KN-8437-11A-01D-2311-10 | g.chr15:70386891_70386892insA | c.213_214insT | c.(211-216)ttgaacfs | p.N72fs |
KIRC | 15 | 70351055 | 70351055 | + | Missense_Mutation | SNP | A | A | T | TCGA-B0-5703-01A-11D-1534-10 | TCGA-B0-5703-11A-01D-1534-10 | g.chr15:70351055A>T | c.865T>A | c.(865-867)Tcg>Acg | p.S289T |
KIRC | 15 | 70368448 | 70368448 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-B8-4622-01A-02D-1553-08 | TCGA-B8-4622-11A-01D-1553-08 | g.chr15:70368448delA | c.284delT | c.(283-285)ttcfs | p.F95fs |
KIRP | 15 | 70368460 | 70368460 | + | Missense_Mutation | SNP | T | T | A | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr15:70368460T>A | c.272A>T | c.(271-273)cAg>cTg | p.Q91L |
LGG | 15 | 70347546 | 70347546 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:70347546C>T | c.1429G>A | c.(1429-1431)Gcc>Acc | p.A477T |
LGG | 15 | 70347560 | 70347560 | + | Missense_Mutation | SNP | C | C | T | TCGA-P5-A731-01A-11D-A32B-08 | TCGA-P5-A731-10A-01D-A329-08 | g.chr15:70347560C>T | c.1415G>A | c.(1414-1416)gGc>gAc | p.G472D |
LGG | 15 | 70350628 | 70350628 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:70350628G>A | c.921C>T | c.(919-921)aaC>aaT | p.N307N |
LGG | 15 | 70366872 | 70366872 | + | Splice_Site | SNP | C | C | T | TCGA-CS-6670-01A-11D-1893-08 | TCGA-CS-6670-10A-01D-1893-08 | g.chr15:70366872C>T | c.372G>A | c.(370-372)ggG>ggA | p.G124G |
LIHC | 15 | 70358457 | 70358457 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr15:70358457delG | c.473delC | c.(472-474)ccafs | p.P158fs |
LIHC | 15 | 70366931 | 70366931 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZP-A9CV-01A-11D-A382-10 | TCGA-ZP-A9CV-10B-01D-A385-10 | g.chr15:70366931C>T | c.313G>A | c.(313-315)Gcg>Acg | p.A105T |
LUAD | 15 | 70342448 | 70342448 | + | Silent | SNP | C | C | T | TCGA-17-Z049-01A-01W-0746-08 | TCGA-17-Z049-11A-01W-0747-08 | g.chr15:70342448C>T | c.2307G>A | c.(2305-2307)gaG>gaA | p.E769E |
LUAD | 15 | 70342515 | 70342515 | + | Missense_Mutation | SNP | C | C | T | TCGA-67-3771-01A-01D-1040-01 | TCGA-67-3771-10A-01D-1040-01 | g.chr15:70342515C>T | c.2240G>A | c.(2239-2241)tGt>tAt | p.C747Y |
LUAD | 15 | 70345643 | 70345643 | + | Missense_Mutation | SNP | C | C | A | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr15:70345643C>A | c.1906G>T | c.(1906-1908)Ggg>Tgg | p.G636W |
LUAD | 15 | 70347516 | 70347516 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-99-8032-01A-11D-2238-08 | TCGA-99-8032-10A-01D-2238-08 | g.chr15:70347516delC | c.1459delG | c.(1459-1461)gagfs | p.E487fs |
LUAD | 15 | 70348691 | 70348691 | + | Missense_Mutation | SNP | G | G | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr15:70348691G>T | c.1283C>A | c.(1282-1284)cCg>cAg | p.P428Q |
LUAD | 15 | 70358421 | 70358421 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5778-01A-01D-1625-08 | TCGA-64-5778-10A-01D-1625-08 | g.chr15:70358421C>A | c.509G>T | c.(508-510)gGc>gTc | p.G170V |
LUSC | 15 | 70342518 | 70342518 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr15:70342518C>G | c.2237G>C | c.(2236-2238)aGt>aCt | p.S746T |
LUSC | 15 | 70344823 | 70344823 | + | Missense_Mutation | SNP | G | G | T | TCGA-21-1081-01A-01D-1521-08 | TCGA-21-1081-10B-01D-1521-08 | g.chr15:70344823G>T | c.2024C>A | c.(2023-2025)gCt>gAt | p.A675D |
LUSC | 15 | 70347520 | 70347520 | + | Silent | SNP | G | G | A | TCGA-66-2744-01A-01D-0983-08 | TCGA-66-2744-11A-01D-0983-08 | g.chr15:70347520G>A | c.1455C>T | c.(1453-1455)caC>caT | p.H485H |
LUSC | 15 | 70351006 | 70351006 | + | Missense_Mutation | SNP | C | C | G | TCGA-22-4601-01A-01D-1441-08 | TCGA-22-4601-11A-01D-1441-08 | g.chr15:70351006C>G | c.914G>C | c.(913-915)gGt>gCt | p.G305A |
LUSC | 15 | 70351076 | 70351076 | + | Missense_Mutation | SNP | C | C | G | TCGA-46-6025-01A-11D-1817-08 | TCGA-46-6025-10A-01D-1817-08 | g.chr15:70351076C>G | c.844G>C | c.(844-846)Gat>Cat | p.D282H |
LUSC | 15 | 70351755 | 70351755 | + | Silent | SNP | G | G | A | TCGA-66-2780-01A-01D-1522-08 | TCGA-66-2780-11A-01D-1522-08 | g.chr15:70351755G>A | c.759C>T | c.(757-759)tcC>tcT | p.S253S |
OV | 15 | 70350516 | 70350516 | + | Missense_Mutation | SNP | G | G | A | TCGA-61-1913-01A-01W-0639-09 | TCGA-61-1913-11A-01W-0640-09 | g.chr15:70350516G>A | c.1033C>T | c.(1033-1035)Ccg>Tcg | p.P345S |
PAAD | 15 | 70358362 | 70358362 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:70358362C>T | c.568G>A | c.(568-570)Gat>Aat | p.D190N |
PRAD | 15 | 70347431 | 70347431 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:70347431C>T | c.1544G>A | c.(1543-1545)aGc>aAc | p.S515N |
PRAD | 15 | 70347600 | 70347600 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZG-A9LS-01A-12D-A41K-08 | TCGA-ZG-A9LS-10A-01D-A41N-08 | g.chr15:70347600G>T | c.1375C>A | c.(1375-1377)Cag>Aag | p.Q459K |
PRAD | 15 | 70352868 | 70352868 | + | Splice_Site | SNP | C | C | T | TCGA-V1-A8WL-01A-11D-A377-08 | TCGA-V1-A8WL-10A-01D-A37A-08 | g.chr15:70352868C>T | | c.e9+1 | |
READ | 15 | 70345690 | 70345690 | + | Missense_Mutation | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:70345690C>T | c.1859G>A | c.(1858-1860)gGg>gAg | p.G620E |
SARC | 15 | 70347560 | 70347560 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-AATS-01A-12D-A417-09 | TCGA-DX-AATS-10A-01D-A41A-09 | g.chr15:70347560C>T | c.1415G>A | c.(1414-1416)gGc>gAc | p.G472D |
SKCM | 15 | 70342442 | 70342442 | + | Silent | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr15:70342442G>A | c.2313C>T | c.(2311-2313)atC>atT | p.I771I |
SKCM | 15 | 70346850 | 70346850 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr15:70346850C>T | c.1762G>A | c.(1762-1764)Gcc>Acc | p.A588T |
SKCM | 15 | 70347595 | 70347595 | + | Silent | SNP | G | G | A | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr15:70347595G>A | c.1380C>T | c.(1378-1380)ccC>ccT | p.P460P |
SKCM | 15 | 70348702 | 70348702 | + | Silent | SNP | G | G | A | TCGA-EE-A2GD-06A-11D-A196-08 | TCGA-EE-A2GD-10A-01D-A198-08 | g.chr15:70348702G>A | c.1272C>T | c.(1270-1272)gaC>gaT | p.D424D |
SKCM | 15 | 70351115 | 70351115 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29X-06A-11D-A196-08 | TCGA-EE-A29X-10A-01D-A198-08 | g.chr15:70351115G>A | c.805C>T | c.(805-807)Cct>Tct | p.P269S |
SKCM | 15 | 70368486 | 70368486 | + | Silent | SNP | C | C | T | TCGA-EE-A2M8-06A-12D-A196-08 | TCGA-EE-A2M8-10A-01D-A198-08 | g.chr15:70368486C>T | c.246G>A | c.(244-246)gcG>gcA | p.A82A |