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 | 52416714 | 52416714 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr15:52416714C>T | c.1132G>A | c.(1132-1134)Gat>Aat | p.D378N |
BLCA | 15 | 52416747 | 52416747 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr15:52416747C>T | c.1099G>A | c.(1099-1101)Gaa>Aaa | p.E367K |
BRCA | 15 | 52416711 | 52416711 | + | Missense_Mutation | SNP | C | C | T | TCGA-AR-A5QN-01A-12D-A28B-09 | TCGA-AR-A5QN-10A-01D-A28E-09 | g.chr15:52416711C>T | c.1135G>A | c.(1135-1137)Ggg>Agg | p.G379R |
BRCA | 15 | 52446168 | 52446168 | + | Missense_Mutation | SNP | T | T | C | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr15:52446168T>C | c.344A>G | c.(343-345)aAa>aGa | p.K115R |
CESC | 15 | 52416673 | 52416673 | + | Silent | SNP | G | G | T | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr15:52416673G>T | c.1173C>A | c.(1171-1173)ctC>ctA | p.L391L |
CESC | 15 | 52418211 | 52418211 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-C5-A7CJ-01A-11D-A32I-09 | TCGA-C5-A7CJ-10A-01D-A32I-09 | g.chr15:52418211C>A | c.943G>T | c.(943-945)Gag>Tag | p.E315* |
CESC | 15 | 52427908 | 52427908 | + | Missense_Mutation | SNP | C | C | G | TCGA-HM-A4S6-01A-11D-A26G-09 | TCGA-HM-A4S6-10A-01D-A26G-09 | g.chr15:52427908C>G | c.673G>C | c.(673-675)Gag>Cag | p.E225Q |
CESC | 15 | 52446256 | 52446256 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A7CL-01A-11D-A32I-09 | TCGA-C5-A7CL-10A-01D-A32I-09 | g.chr15:52446256G>A | c.256C>T | c.(256-258)Cgg>Tgg | p.R86W |
CESC | 15 | 52472036 | 52472036 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr15:52472036G>T | c.167C>A | c.(166-168)tCg>tAg | p.S56* |
COAD | 15 | 52416738 | 52416738 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5537-01A-21D-1924-10 | TCGA-D5-5537-10A-01D-1924-10 | g.chr15:52416738C>T | c.1108G>A | c.(1108-1110)Gtt>Att | p.V370I |
COAD | 15 | 52416741 | 52416741 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr15:52416741G>A | c.1105C>T | c.(1105-1107)Cgc>Tgc | p.R369C |
COAD | 15 | 52425628 | 52425628 | + | Silent | SNP | G | G | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr15:52425628G>A | c.810C>T | c.(808-810)tcC>tcT | p.S270S |
COAD | 15 | 52427938 | 52427938 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:52427938C>T | c.643G>A | c.(643-645)Ggc>Agc | p.G215S |
COAD | 15 | 52446143 | 52446143 | + | Silent | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:52446143C>T | c.369G>A | c.(367-369)tcG>tcA | p.S123S |
COADREAD | 15 | 52416738 | 52416738 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5537-01A-21D-1924-10 | TCGA-D5-5537-10A-01D-1924-10 | g.chr15:52416738C>T | c.1108G>A | c.(1108-1110)Gtt>Att | p.V370I |
COADREAD | 15 | 52416741 | 52416741 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr15:52416741G>A | c.1105C>T | c.(1105-1107)Cgc>Tgc | p.R369C |
COADREAD | 15 | 52425628 | 52425628 | + | Silent | SNP | G | G | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr15:52425628G>A | c.810C>T | c.(808-810)tcC>tcT | p.S270S |
COADREAD | 15 | 52427938 | 52427938 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:52427938C>T | c.643G>A | c.(643-645)Ggc>Agc | p.G215S |
COADREAD | 15 | 52446143 | 52446143 | + | Silent | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr15:52446143C>T | c.369G>A | c.(367-369)tcG>tcA | p.S123S |
DLBC | 15 | 52433397 | 52433397 | + | Silent | SNP | C | C | T | TCGA-G8-6326-01A-11D-2210-10 | TCGA-G8-6326-10A-01D-2210-10 | g.chr15:52433397C>T | c.567G>A | c.(565-567)aaG>aaA | p.K189K |
DLBC | 15 | 52433397 | 52433397 | + | Silent | SNP | C | C | T | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr15:52433397C>T | c.567G>A | c.(565-567)aaG>aaA | p.K189K |
DLBC | 15 | 52446260 | 52446260 | + | Silent | SNP | C | C | T | TCGA-G8-6326-01A-11D-2210-10 | TCGA-G8-6326-10A-01D-2210-10 | g.chr15:52446260C>T | c.252G>A | c.(250-252)gcG>gcA | p.A84A |
DLBC | 15 | 52446260 | 52446260 | + | Silent | SNP | C | C | T | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr15:52446260C>T | c.252G>A | c.(250-252)gcG>gcA | p.A84A |
ESCA | 15 | 52425597 | 52425597 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A9FO-01A-11D-A387-09 | TCGA-LN-A9FO-10A-01D-A38A-09 | g.chr15:52425597C>T | c.841G>A | c.(841-843)Gaa>Aaa | p.E281K |
GBMLGG | 15 | 52446271 | 52446271 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:52446271G>A | c.241C>T | c.(241-243)Cac>Tac | p.H81Y |
HNSC | 15 | 52427914 | 52427914 | + | Missense_Mutation | SNP | C | C | T | TCGA-MT-A7BN-01A-12D-A34J-08 | TCGA-MT-A7BN-10A-01D-A34M-08 | g.chr15:52427914C>T | c.667G>A | c.(667-669)Gac>Aac | p.D223N |
HNSC | 15 | 52446255 | 52446255 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-7368-01A-11D-2129-08 | TCGA-CR-7368-10A-01D-2129-08 | g.chr15:52446255C>T | c.257G>A | c.(256-258)cGg>cAg | p.R86Q |
KIPAN | 15 | 52425644 | 52425644 | + | Missense_Mutation | SNP | A | A | G | TCGA-UZ-A9PX-01A-11D-A42J-10 | TCGA-UZ-A9PX-10A-01D-A42M-10 | g.chr15:52425644A>G | c.794T>C | c.(793-795)gTg>gCg | p.V265A |
KIPAN | 15 | 52433455 | 52433455 | + | Missense_Mutation | SNP | T | T | G | TCGA-BP-4347-01A-01D-1366-10 | TCGA-BP-4347-11A-01D-1366-10 | g.chr15:52433455T>G | c.509A>C | c.(508-510)aAg>aCg | p.K170T |
KIPAN | 15 | 52446239 | 52446239 | + | Silent | SNP | C | C | T | TCGA-A4-7997-01A-11D-2201-08 | TCGA-A4-7997-10A-01D-2201-08 | g.chr15:52446239C>T | c.273G>A | c.(271-273)ggG>ggA | p.G91G |
KIPAN | 15 | 52476835 | 52476835 | + | Silent | SNP | T | T | G | TCGA-BP-5191-01A-01D-1429-08 | TCGA-BP-5191-11A-01D-1429-08 | g.chr15:52476835T>G | c.39A>C | c.(37-39)tcA>tcC | p.S13S |
KIRC | 15 | 52433455 | 52433455 | + | Missense_Mutation | SNP | T | T | G | TCGA-BP-4347-01A-01D-1366-10 | TCGA-BP-4347-11A-01D-1366-10 | g.chr15:52433455T>G | c.509A>C | c.(508-510)aAg>aCg | p.K170T |
KIRC | 15 | 52476835 | 52476835 | + | Silent | SNP | T | T | G | TCGA-BP-5191-01A-01D-1429-08 | TCGA-BP-5191-11A-01D-1429-08 | g.chr15:52476835T>G | c.39A>C | c.(37-39)tcA>tcC | p.S13S |
KIRP | 15 | 52425644 | 52425644 | + | Missense_Mutation | SNP | A | A | G | TCGA-UZ-A9PX-01A-11D-A42J-10 | TCGA-UZ-A9PX-10A-01D-A42M-10 | g.chr15:52425644A>G | c.794T>C | c.(793-795)gTg>gCg | p.V265A |
KIRP | 15 | 52446239 | 52446239 | + | Silent | SNP | C | C | T | TCGA-A4-7997-01A-11D-2201-08 | TCGA-A4-7997-10A-01D-2201-08 | g.chr15:52446239C>T | c.273G>A | c.(271-273)ggG>ggA | p.G91G |
LGG | 15 | 52446271 | 52446271 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:52446271G>A | c.241C>T | c.(241-243)Cac>Tac | p.H81Y |
LIHC | 15 | 52416719 | 52416719 | + | Missense_Mutation | SNP | G | G | A | TCGA-G3-AAV3-01A-11D-A36X-10 | TCGA-G3-AAV3-10A-01D-A370-10 | g.chr15:52416719G>A | c.1127C>T | c.(1126-1128)tCc>tTc | p.S376F |
LIHC | 15 | 52418147 | 52418147 | + | Missense_Mutation | SNP | C | C | A | TCGA-BC-A10U-01A-11D-A12Z-10 | TCGA-BC-A10U-11A-11D-A12Z-10 | g.chr15:52418147C>A | c.1007G>T | c.(1006-1008)aGt>aTt | p.S336I |
LIHC | 15 | 52476791 | 52476791 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-A1EE-01A-11D-A12Z-10 | TCGA-DD-A1EE-10A-01D-A12Z-10 | g.chr15:52476791T>A | c.83A>T | c.(82-84)aAg>aTg | p.K28M |
LIHC | 15 | 52476791 | 52476791 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-A1EJ-01A-11D-A152-10 | TCGA-DD-A1EJ-10A-01D-A152-10 | g.chr15:52476791T>A | c.83A>T | c.(82-84)aAg>aTg | p.K28M |
LUAD | 15 | 52418243 | 52418243 | + | Splice_Site | SNP | T | T | C | TCGA-05-4389-01A-01D-1265-08 | TCGA-05-4389-10A-01D-1265-08 | g.chr15:52418243T>C | | c.e11-2 | |
LUAD | 15 | 52420406 | 52420406 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr15:52420406G>A | c.899C>T | c.(898-900)tCa>tTa | p.S300L |
LUAD | 15 | 52433340 | 52433340 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-7948-01A-11D-2184-08 | TCGA-95-7948-10A-01D-2184-08 | g.chr15:52433340C>T | c.624G>A | c.(622-624)atG>atA | p.M208I |
LUAD | 15 | 52442101 | 52442101 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chr15:52442101C>A | c.397G>T | c.(397-399)Gat>Tat | p.D133Y |
LUAD | 15 | 52446250 | 52446250 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8076-01A-31D-2238-08 | TCGA-86-8076-10A-01D-2238-08 | g.chr15:52446250C>G | c.262G>C | c.(262-264)Gag>Cag | p.E88Q |
LUAD | 15 | 52472025 | 52472025 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr15:52472025C>A | c.178G>T | c.(178-180)Gag>Tag | p.E60* |
LUAD | 15 | 52476783 | 52476783 | + | Missense_Mutation | SNP | G | G | C | TCGA-NJ-A4YP-01A-11D-A25L-08 | TCGA-NJ-A4YP-10A-01D-A25L-08 | g.chr15:52476783G>C | c.91C>G | c.(91-93)Caa>Gaa | p.Q31E |
LUSC | 15 | 52420404 | 52420404 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-5239-01A-21D-1817-08 | TCGA-34-5239-10A-01D-1817-08 | g.chr15:52420404C>T | c.901G>A | c.(901-903)Gat>Aat | p.D301N |
PAAD | 15 | 52425618 | 52425618 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:52425618C>T | c.820G>A | c.(820-822)Gtg>Atg | p.V274M |
PRAD | 15 | 52433404 | 52433404 | + | Missense_Mutation | SNP | T | T | C | TCGA-EJ-5519-01A-01D-1576-08 | TCGA-EJ-5519-10A-01D-1577-08 | g.chr15:52433404T>C | c.560A>G | c.(559-561)aAa>aGa | p.K187R |
SKCM | 15 | 52416676 | 52416676 | + | Silent | SNP | G | G | A | TCGA-D3-A2J7-06A-11D-A196-08 | TCGA-D3-A2J7-10A-01D-A198-08 | g.chr15:52416676G>A | c.1170C>T | c.(1168-1170)acC>acT | p.T390T |
SKCM | 15 | 52418213 | 52418213 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr15:52418213C>T | c.941G>A | c.(940-942)aGg>aAg | p.R314K |
SKCM | 15 | 52433395 | 52433395 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr15:52433395G>A | c.569C>T | c.(568-570)tCt>tTt | p.S190F |
SKCM | 15 | 52446245 | 52446245 | + | Silent | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr15:52446245G>A | c.267C>T | c.(265-267)gcC>gcT | p.A89A |