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 |
BRCA | 15 | 78580711 | 78580711 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-GM-A2DD-01A-11D-A17W-09 | TCGA-GM-A2DD-10C-01D-A17W-09 | g.chr15:78580711delG | c.576delC | c.(574-576)cccfs | p.P192fs |
BRCA | 15 | 78585121 | 78585121 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr15:78585121C>G | c.156G>C | c.(154-156)gaG>gaC | p.E52D |
CESC | 15 | 78577611 | 78577611 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr15:78577611G>A | c.820C>T | c.(820-822)Cag>Tag | p.Q274* |
CHOL | 15 | 78580718 | 78580718 | + | Missense_Mutation | SNP | G | G | T | TCGA-W5-AA2Q-01A-11D-A417-09 | TCGA-W5-AA2Q-10A-01D-A41A-09 | g.chr15:78580718G>T | c.569C>A | c.(568-570)gCc>gAc | p.A190D |
CHOL | 15 | 78582401 | 78582401 | + | Silent | SNP | A | A | G | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr15:78582401A>G | c.360T>C | c.(358-360)taT>taC | p.Y120Y |
COAD | 15 | 78577679 | 78577679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:78577679G>A | c.752C>T | c.(751-753)tCg>tTg | p.S251L |
COAD | 15 | 78580639 | 78580639 | + | Silent | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr15:78580639G>A | c.648C>T | c.(646-648)atC>atT | p.I216I |
COAD | 15 | 78580688 | 78580688 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:78580688G>A | c.599C>T | c.(598-600)cCg>cTg | p.P200L |
COAD | 15 | 78580718 | 78580718 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr15:78580718G>A | c.569C>T | c.(568-570)gCc>gTc | p.A190V |
COAD | 15 | 78581977 | 78581977 | + | Silent | SNP | A | A | T | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr15:78581977A>T | c.546T>A | c.(544-546)ctT>ctA | p.L182L |
COAD | 15 | 78585066 | 78585067 | + | Missense_Mutation | DNP | CC | CC | AA | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr15:78585066_78585067CC>AA | c.210_211GG>TT | c.(208-213)gtGGac>gtTTac | p.D71Y |
COADREAD | 15 | 78577679 | 78577679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:78577679G>A | c.752C>T | c.(751-753)tCg>tTg | p.S251L |
COADREAD | 15 | 78580639 | 78580639 | + | Silent | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr15:78580639G>A | c.648C>T | c.(646-648)atC>atT | p.I216I |
COADREAD | 15 | 78580688 | 78580688 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:78580688G>A | c.599C>T | c.(598-600)cCg>cTg | p.P200L |
COADREAD | 15 | 78580718 | 78580718 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr15:78580718G>A | c.569C>T | c.(568-570)gCc>gTc | p.A190V |
COADREAD | 15 | 78581977 | 78581977 | + | Silent | SNP | A | A | T | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr15:78581977A>T | c.546T>A | c.(544-546)ctT>ctA | p.L182L |
COADREAD | 15 | 78581978 | 78581978 | + | Missense_Mutation | SNP | A | A | G | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr15:78581978A>G | c.545T>C | c.(544-546)cTt>cCt | p.L182P |
COADREAD | 15 | 78585066 | 78585067 | + | Missense_Mutation | DNP | CC | CC | AA | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr15:78585066_78585067CC>AA | c.210_211GG>TT | c.(208-213)gtGGac>gtTTac | p.D71Y |
ESCA | 15 | 78580699 | 78580699 | + | Missense_Mutation | SNP | C | C | G | TCGA-IG-A51D-01A-11D-A27G-09 | TCGA-IG-A51D-10A-01D-A27G-09 | g.chr15:78580699C>G | c.588G>C | c.(586-588)ttG>ttC | p.L196F |
GBM | 15 | 78578420 | 78578420 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr15:78578420C>T | c.712G>A | c.(712-714)Gtt>Att | p.V238I |
GBMLGG | 15 | 78578420 | 78578420 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr15:78578420C>T | c.712G>A | c.(712-714)Gtt>Att | p.V238I |
LIHC | 15 | 78582307 | 78582307 | + | Missense_Mutation | SNP | G | G | C | TCGA-DD-AACZ-01A-11D-A40R-10 | TCGA-DD-AACZ-10A-01D-A40U-10 | g.chr15:78582307G>C | c.454C>G | c.(454-456)Ctt>Gtt | p.L152V |
LUAD | 15 | 78577629 | 78577629 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr15:78577629G>A | c.802C>T | c.(802-804)Cac>Tac | p.H268Y |
LUAD | 15 | 78585583 | 78585583 | + | Missense_Mutation | SNP | C | C | A | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr15:78585583C>A | c.72G>T | c.(70-72)tgG>tgT | p.W24C |
OV | 15 | 78575864 | 78575864 | + | Splice_Site | SNP | C | C | T | TCGA-61-1895-01A-01W-0639-09 | TCGA-61-1895-11A-01W-0639-09 | g.chr15:78575864C>T | | c.e11-1 | |
OV | 15 | 78581979 | 78581979 | + | Missense_Mutation | SNP | G | G | A | TCGA-13-0755-01A-01W-0372-09 | TCGA-13-0755-10A-01W-0372-09 | g.chr15:78581979G>A | c.544C>T | c.(544-546)Ctt>Ttt | p.L182F |
PAAD | 15 | 78585111 | 78585111 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:78585111G>T | c.166C>A | c.(166-168)Cta>Ata | p.L56I |
READ | 15 | 78581978 | 78581978 | + | Missense_Mutation | SNP | A | A | G | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr15:78581978A>G | c.545T>C | c.(544-546)cTt>cCt | p.L182P |
SKCM | 15 | 78580681 | 78580681 | + | Silent | SNP | G | G | A | TCGA-EE-A2MH-06A-11D-A197-08 | TCGA-EE-A2MH-10A-01D-A199-08 | g.chr15:78580681G>A | c.606C>T | c.(604-606)tcC>tcT | p.S202S |