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 | 77323595 | 77323595 | + | Silent | SNP | C | C | T | TCGA-DK-A3IL-01A-11D-A20D-08 | TCGA-DK-A3IL-10A-01D-A20D-08 | g.chr15:77323595C>T | c.717C>T | c.(715-717)tcC>tcT | p.S239S |
BLCA | 15 | 77324701 | 77324701 | + | Silent | SNP | C | C | T | TCGA-DK-AA71-01A-31D-A391-08 | TCGA-DK-AA71-10A-01D-A394-08 | g.chr15:77324701C>T | c.804C>T | c.(802-804)ttC>ttT | p.F268F |
BLCA | 15 | 77328221 | 77328221 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr15:77328221G>A | c.1064G>A | c.(1063-1065)gGa>gAa | p.G355E |
BRCA | 15 | 77310845 | 77310845 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A0YM-01A-11D-A10G-09 | TCGA-A2-A0YM-10A-01D-A10G-09 | g.chr15:77310845G>A | c.185G>A | c.(184-186)cGg>cAg | p.R62Q |
BRCA | 15 | 77310855 | 77310855 | + | Silent | SNP | T | T | G | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr15:77310855T>G | c.195T>G | c.(193-195)ggT>ggG | p.G65G |
CESC | 15 | 77310554 | 77310554 | + | Silent | SNP | G | G | A | TCGA-EX-A1H6-01B-11D-A22X-09 | TCGA-EX-A1H6-10A-01D-A22X-09 | g.chr15:77310554G>A | c.102G>A | c.(100-102)aaG>aaA | p.K34K |
CESC | 15 | 77317846 | 77317846 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A852-01A-11D-A351-09 | TCGA-JW-A852-10A-01D-A351-09 | g.chr15:77317846G>C | c.255G>C | c.(253-255)gaG>gaC | p.E85D |
COAD | 15 | 77320234 | 77320234 | + | Silent | SNP | G | G | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr15:77320234G>A | c.396G>A | c.(394-396)tcG>tcA | p.S132S |
COAD | 15 | 77324684 | 77324684 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr15:77324684G>A | c.787G>A | c.(787-789)Gcc>Acc | p.A263T |
COAD | 15 | 77328147 | 77328147 | + | Silent | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr15:77328147C>A | c.990C>A | c.(988-990)tcC>tcA | p.S330S |
COADREAD | 15 | 77320234 | 77320234 | + | Silent | SNP | G | G | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr15:77320234G>A | c.396G>A | c.(394-396)tcG>tcA | p.S132S |
COADREAD | 15 | 77324684 | 77324684 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr15:77324684G>A | c.787G>A | c.(787-789)Gcc>Acc | p.A263T |
COADREAD | 15 | 77328147 | 77328147 | + | Silent | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr15:77328147C>A | c.990C>A | c.(988-990)tcC>tcA | p.S330S |
ESCA | 15 | 77310810 | 77310810 | + | Missense_Mutation | SNP | G | G | T | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr15:77310810G>T | c.150G>T | c.(148-150)gaG>gaT | p.E50D |
ESCA | 15 | 77310844 | 77310844 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A88Z-01A-11D-A36J-09 | TCGA-L5-A88Z-11A-11D-A36M-09 | g.chr15:77310844C>T | c.184C>T | c.(184-186)Cgg>Tgg | p.R62W |
ESCA | 15 | 77310871 | 77310874 | + | Splice_Site | DEL | AAGT | AAGT | - | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr15:77310871_77310874delAAGT | c.211_212delAAGT | c.(211-213)aag>g | p.K71fs |
ESCA | 15 | 77320223 | 77320223 | + | Missense_Mutation | SNP | A | A | T | TCGA-L5-A4OP-01A-11D-A27G-09 | TCGA-L5-A4OP-11A-11D-A27G-09 | g.chr15:77320223A>T | c.385A>T | c.(385-387)Agc>Tgc | p.S129C |
ESCA | 15 | 77323585 | 77323585 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A8NS-01A-12D-A37C-09 | TCGA-L5-A8NS-11A-11D-A37F-09 | g.chr15:77323585A>G | c.707A>G | c.(706-708)aAc>aGc | p.N236S |
HNSC | 15 | 77310547 | 77310547 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7097-01A-11D-2012-08 | TCGA-CV-7097-11A-01D-2012-08 | g.chr15:77310547G>A | c.95G>A | c.(94-96)gGc>gAc | p.G32D |
HNSC | 15 | 77324641 | 77324641 | + | Silent | SNP | C | C | G | TCGA-HD-A633-01A-11D-A28R-08 | TCGA-HD-A633-10A-01D-A28U-08 | g.chr15:77324641C>G | c.744C>G | c.(742-744)ctC>ctG | p.L248L |
LIHC | 15 | 77310567 | 77310567 | + | Missense_Mutation | SNP | A | A | T | TCGA-T1-A6J8-01A-11D-A32G-10 | TCGA-T1-A6J8-10A-01D-A32G-10 | g.chr15:77310567A>T | c.115A>T | c.(115-117)Atg>Ttg | p.M39L |
LIHC | 15 | 77310799 | 77310799 | + | Splice_Site | SNP | G | G | T | TCGA-CC-A8HV-01A-11D-A35Z-10 | TCGA-CC-A8HV-10A-01D-A35Z-10 | g.chr15:77310799G>T | c.139G>T | c.(139-141)Gcc>Tcc | p.A47S |
LIHC | 15 | 77320208 | 77320208 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-AADO-01A-11D-A40R-10 | TCGA-DD-AADO-10A-01D-A40U-10 | g.chr15:77320208G>T | c.370G>T | c.(370-372)Gac>Tac | p.D124Y |
LIHC | 15 | 77320928 | 77320928 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-AAW0-01A-11D-A40R-10 | TCGA-DD-AAW0-10A-01D-A40U-10 | g.chr15:77320928G>T | c.451G>T | c.(451-453)Gcg>Tcg | p.A151S |
LUAD | 15 | 77310589 | 77310589 | + | Splice_Site | SNP | G | G | C | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr15:77310589G>C | c.137G>C | c.(136-138)aGg>aCg | p.R46T |
LUAD | 15 | 77317631 | 77317631 | + | Silent | SNP | G | G | A | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr15:77317631G>A | c.219G>A | c.(217-219)ctG>ctA | p.L73L |
LUAD | 15 | 77317648 | 77317648 | + | Missense_Mutation | SNP | C | C | T | TCGA-97-8176-01A-11D-2393-08 | TCGA-97-8176-10B-01D-2393-08 | g.chr15:77317648C>T | c.236C>T | c.(235-237)tCc>tTc | p.S79F |
LUAD | 15 | 77324705 | 77324705 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-8640-01A-11D-2393-08 | TCGA-78-8640-11A-01D-2393-08 | g.chr15:77324705C>A | c.808C>A | c.(808-810)Cag>Aag | p.Q270K |
LUAD | 15 | 77325276 | 77325276 | + | Silent | SNP | C | C | A | TCGA-69-7973-01A-11D-2184-08 | TCGA-69-7973-10A-01D-2184-08 | g.chr15:77325276C>A | c.912C>A | c.(910-912)tcC>tcA | p.S304S |
LUAD | 15 | 77329395 | 77329395 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7149-01A-11D-2036-08 | TCGA-78-7149-10A-01D-2036-08 | g.chr15:77329395G>A | c.1129G>A | c.(1129-1131)Gag>Aag | p.E377K |
LUAD | 15 | 77329423 | 77329423 | + | Missense_Mutation | SNP | T | T | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr15:77329423T>A | c.1157T>A | c.(1156-1158)cTg>cAg | p.L386Q |
LUSC | 15 | 77310525 | 77310525 | + | Missense_Mutation | SNP | C | C | A | TCGA-70-6722-01A-11D-1817-08 | TCGA-70-6722-10A-01D-1817-08 | g.chr15:77310525C>A | c.73C>A | c.(73-75)Ctg>Atg | p.L25M |
LUSC | 15 | 77328172 | 77328172 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2727-01A-01D-0983-08 | TCGA-66-2727-11A-01D-0983-08 | g.chr15:77328172G>A | c.1015G>A | c.(1015-1017)Gag>Aag | p.E339K |
OV | 15 | 77310554 | 77310554 | + | Missense_Mutation | SNP | G | G | C | TCGA-13-0900-01B-01W-0490-10 | TCGA-13-0900-10A-01W-0490-10 | g.chr15:77310554G>C | c.102G>C | c.(100-102)aaG>aaC | p.K34N |
PAAD | 15 | 77325208 | 77325208 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:77325208G>A | c.844G>A | c.(844-846)Gtg>Atg | p.V282M |
SARC | 15 | 77317931 | 77317931 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr15:77317931G>A | c.340G>A | c.(340-342)Gag>Aag | p.E114K |
SKCM | 15 | 77310494 | 77310494 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:77310494G>A | c.42G>A | c.(40-42)agG>agA | p.R14R |
SKCM | 15 | 77310494 | 77310494 | + | Silent | SNP | G | G | A | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr15:77310494G>A | c.42G>A | c.(40-42)agG>agA | p.R14R |
SKCM | 15 | 77317640 | 77317640 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:77317640C>T | c.228C>T | c.(226-228)tcC>tcT | p.S76S |
SKCM | 15 | 77320971 | 77320971 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EA-06A-11D-A30X-08 | TCGA-D9-A6EA-10A-01D-A30X-08 | g.chr15:77320971G>A | c.494G>A | c.(493-495)gGc>gAc | p.G165D |
SKCM | 15 | 77324710 | 77324710 | + | Silent | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr15:77324710C>T | c.813C>T | c.(811-813)gcC>gcT | p.A271A |