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 | 7 | 26709767 | 26709767 | + | Silent | SNP | G | G | A | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr7:26709767G>A | c.1032C>T | c.(1030-1032)gcC>gcT | p.A344A |
BLCA | 7 | 26709771 | 26709771 | + | Missense_Mutation | SNP | C | C | T | TCGA-BL-A3JM-01A-12D-A21A-08 | TCGA-BL-A3JM-11A-31D-A21A-08 | g.chr7:26709771C>T | c.1028G>A | c.(1027-1029)gGa>gAa | p.G343E |
BLCA | 7 | 26765126 | 26765126 | + | Silent | SNP | A | A | G | TCGA-GC-A6I3-01A-11D-A31L-08 | TCGA-GC-A6I3-10A-01D-A31J-08 | g.chr7:26765126A>G | c.717T>C | c.(715-717)gaT>gaC | p.D239D |
BRCA | 7 | 26765161 | 26765161 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:26765161C>T | c.682G>A | c.(682-684)Gag>Aag | p.E228K |
BRCA | 7 | 26778477 | 26778477 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr7:26778477C>G | c.406G>C | c.(406-408)Gaa>Caa | p.E136Q |
CESC | 7 | 26883654 | 26883654 | + | Missense_Mutation | SNP | G | G | A | TCGA-DG-A2KM-01A-11D-A17W-09 | TCGA-DG-A2KM-10A-01D-A17W-09 | g.chr7:26883654G>A | c.302C>T | c.(301-303)tCt>tTt | p.S101F |
COAD | 7 | 26709785 | 26709785 | + | Silent | SNP | T | T | C | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr7:26709785T>C | c.1014A>G | c.(1012-1014)gtA>gtG | p.V338V |
COAD | 7 | 26766511 | 26766511 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3543-01A-01W-0833-10 | TCGA-AA-3543-10A-01W-0833-10 | g.chr7:26766511C>T | c.584G>A | c.(583-585)cGt>cAt | p.R195H |
COAD | 7 | 26766622 | 26766622 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:26766622T>C | c.473A>G | c.(472-474)aAa>aGa | p.K158R |
COAD | 7 | 26894417 | 26894417 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:26894417C>A | c.160G>T | c.(160-162)Gat>Tat | p.D54Y |
COAD | 7 | 26894420 | 26894420 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr7:26894420T>G | c.157A>C | c.(157-159)Aaa>Caa | p.K53Q |
COADREAD | 7 | 26709785 | 26709785 | + | Silent | SNP | T | T | C | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr7:26709785T>C | c.1014A>G | c.(1012-1014)gtA>gtG | p.V338V |
COADREAD | 7 | 26766511 | 26766511 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3543-01A-01W-0833-10 | TCGA-AA-3543-10A-01W-0833-10 | g.chr7:26766511C>T | c.584G>A | c.(583-585)cGt>cAt | p.R195H |
COADREAD | 7 | 26766622 | 26766622 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:26766622T>C | c.473A>G | c.(472-474)aAa>aGa | p.K158R |
COADREAD | 7 | 26778460 | 26778460 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr7:26778460C>A | c.423G>T | c.(421-423)tgG>tgT | p.W141C |
COADREAD | 7 | 26894417 | 26894417 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:26894417C>A | c.160G>T | c.(160-162)Gat>Tat | p.D54Y |
COADREAD | 7 | 26894420 | 26894420 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr7:26894420T>G | c.157A>C | c.(157-159)Aaa>Caa | p.K53Q |
ESCA | 7 | 26709727 | 26709727 | + | Missense_Mutation | SNP | C | C | G | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr7:26709727C>G | c.1072G>C | c.(1072-1074)Gat>Cat | p.D358H |
ESCA | 7 | 26779515 | 26779515 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A88V-01A-11D-A351-09 | TCGA-L5-A88V-11A-11D-A351-09 | g.chr7:26779515G>A | c.376C>T | c.(376-378)Cgc>Tgc | p.R126C |
ESCA | 7 | 26779515 | 26779515 | + | Missense_Mutation | SNP | G | G | A | TCGA-R6-A6L6-01B-11D-A33E-09 | TCGA-R6-A6L6-10A-01D-A33H-09 | g.chr7:26779515G>A | c.376C>T | c.(376-378)Cgc>Tgc | p.R126C |
GBM | 7 | 26766511 | 26766511 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0644-01A-02D-1492-08 | TCGA-06-0644-10A-01D-1492-08 | g.chr7:26766511C>T | c.584G>A | c.(583-585)cGt>cAt | p.R195H |
GBM | 7 | 26778465 | 26778465 | + | Missense_Mutation | SNP | G | G | A | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr7:26778465G>A | c.418C>T | c.(418-420)Cgg>Tgg | p.R140W |
GBM | 7 | 26779515 | 26779515 | + | Missense_Mutation | SNP | G | G | A | TCGA-76-6191-01A-12D-1696-08 | TCGA-76-6191-10A-01D-1696-08 | g.chr7:26779515G>A | c.376C>T | c.(376-378)Cgc>Tgc | p.R126C |
GBMLGG | 7 | 26729921 | 26729921 | + | Missense_Mutation | SNP | C | C | T | TCGA-DB-A64W-01A-11D-A29Q-08 | TCGA-DB-A64W-10A-01D-A29Q-08 | g.chr7:26729921C>T | c.857G>A | c.(856-858)aGt>aAt | p.S286N |
GBMLGG | 7 | 26766511 | 26766511 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0644-01A-02D-1492-08 | TCGA-06-0644-10A-01D-1492-08 | g.chr7:26766511C>T | c.584G>A | c.(583-585)cGt>cAt | p.R195H |
GBMLGG | 7 | 26778465 | 26778465 | + | Missense_Mutation | SNP | G | G | A | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr7:26778465G>A | c.418C>T | c.(418-420)Cgg>Tgg | p.R140W |
GBMLGG | 7 | 26779515 | 26779515 | + | Missense_Mutation | SNP | G | G | A | TCGA-76-6191-01A-12D-1696-08 | TCGA-76-6191-10A-01D-1696-08 | g.chr7:26779515G>A | c.376C>T | c.(376-378)Cgc>Tgc | p.R126C |
HNSC | 7 | 26778441 | 26778441 | + | Missense_Mutation | SNP | C | C | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr7:26778441C>T | c.442G>A | c.(442-444)Gta>Ata | p.V148I |
HNSC | 7 | 26779555 | 26779555 | + | Silent | SNP | T | T | C | TCGA-CN-5364-01A-01D-1434-08 | TCGA-CN-5364-10A-01D-1434-08 | g.chr7:26779555T>C | c.336A>G | c.(334-336)caA>caG | p.Q112Q |
KIPAN | 7 | 26765559 | 26765559 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4346-01A-01D-1366-10 | TCGA-BP-4346-11A-01D-1366-10 | g.chr7:26765559A>C | c.641T>G | c.(640-642)cTg>cGg | p.L214R |
KIRC | 7 | 26765559 | 26765559 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4346-01A-01D-1366-10 | TCGA-BP-4346-11A-01D-1366-10 | g.chr7:26765559A>C | c.641T>G | c.(640-642)cTg>cGg | p.L214R |
LGG | 7 | 26729921 | 26729921 | + | Missense_Mutation | SNP | C | C | T | TCGA-DB-A64W-01A-11D-A29Q-08 | TCGA-DB-A64W-10A-01D-A29Q-08 | g.chr7:26729921C>T | c.857G>A | c.(856-858)aGt>aAt | p.S286N |
LIHC | 7 | 26765146 | 26765146 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr7:26765146T>C | c.697A>G | c.(697-699)Aga>Gga | p.R233G |
LIHC | 7 | 26765154 | 26765154 | + | Missense_Mutation | SNP | T | T | C | TCGA-BC-A5W4-01A-11D-A28X-10 | TCGA-BC-A5W4-10A-01D-A28X-10 | g.chr7:26765154T>C | c.689A>G | c.(688-690)tAt>tGt | p.Y230C |
LIHC | 7 | 26779530 | 26779530 | + | Missense_Mutation | SNP | C | C | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr7:26779530C>T | c.361G>A | c.(361-363)Ggc>Agc | p.G121S |
LUAD | 7 | 26709737 | 26709737 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr7:26709737C>T | c.1062G>A | c.(1060-1062)atG>atA | p.M354I |
LUAD | 7 | 26709796 | 26709796 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-A4M7-01A-11D-A24P-08 | TCGA-97-A4M7-10A-01D-A24P-08 | g.chr7:26709796C>A | c.1003G>T | c.(1003-1005)Ggc>Tgc | p.G335C |
LUAD | 7 | 26729961 | 26729961 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr7:26729961G>C | c.817C>G | c.(817-819)Cca>Gca | p.P273A |
LUAD | 7 | 26765118 | 26765118 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr7:26765118T>A | c.725A>T | c.(724-726)cAt>cTt | p.H242L |
LUAD | 7 | 26766626 | 26766626 | + | Splice_Site | SNP | C | C | A | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr7:26766626C>A | | c.e7-1 | |
LUAD | 7 | 26778484 | 26778484 | + | Silent | SNP | C | C | A | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr7:26778484C>A | c.399G>T | c.(397-399)ctG>ctT | p.L133L |
LUAD | 7 | 26779578 | 26779578 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr7:26779578G>A | c.313C>T | c.(313-315)Cag>Tag | p.Q105* |
LUSC | 7 | 26729970 | 26729970 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2770-01A-01D-1522-08 | TCGA-66-2770-11A-01D-1522-08 | g.chr7:26729970C>A | c.808G>T | c.(808-810)Gac>Tac | p.D270Y |
LUSC | 7 | 26779509 | 26779509 | + | Missense_Mutation | SNP | T | T | C | TCGA-21-1071-01A-01D-1521-08 | TCGA-21-1071-11A-01D-1521-08 | g.chr7:26779509T>C | c.382A>G | c.(382-384)Aaa>Gaa | p.K128E |
OV | 7 | 26779515 | 26779515 | + | Missense_Mutation | SNP | G | G | A | TCGA-20-1683-01A-01W-0633-09 | TCGA-20-1683-10A-01W-0633-09 | g.chr7:26779515G>A | c.376C>T | c.(376-378)Cgc>Tgc | p.R126C |
PAAD | 7 | 26883668 | 26883668 | + | Silent | SNP | G | G | A | TCGA-HZ-A49I-01A-12D-A26I-08 | TCGA-HZ-A49I-10A-01D-A26I-08 | g.chr7:26883668G>A | c.288C>T | c.(286-288)gaC>gaT | p.D96D |
READ | 7 | 26778460 | 26778460 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr7:26778460C>A | c.423G>T | c.(421-423)tgG>tgT | p.W141C |
SKCM | 7 | 26724414 | 26724414 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr7:26724414C>T | c.928G>A | c.(928-930)Gga>Aga | p.G310R |
SKCM | 7 | 26765109 | 26765109 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr7:26765109G>A | c.734C>T | c.(733-735)cCa>cTa | p.P245L |
SKCM | 7 | 26766566 | 26766566 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:26766566G>A | c.529C>T | c.(529-531)Cta>Tta | p.L177L |
SKCM | 7 | 26766572 | 26766572 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr7:26766572T>A | c.523A>T | c.(523-525)Aac>Tac | p.N175Y |
SKCM | 7 | 26778453 | 26778453 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:26778453G>A | c.430C>T | c.(430-432)Ctc>Ttc | p.L144F |
SKCM | 7 | 26779529 | 26779529 | + | Missense_Mutation | SNP | C | C | A | TCGA-EE-A2A1-06A-11D-A197-08 | TCGA-EE-A2A1-10A-01D-A199-08 | g.chr7:26779529C>A | c.362G>T | c.(361-363)gGc>gTc | p.G121V |
SKCM | 7 | 26883666 | 26883666 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr7:26883666T>C | c.290A>G | c.(289-291)gAt>gGt | p.D97G |
SKCM | 7 | 26883685 | 26883685 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr7:26883685C>T | c.271G>A | c.(271-273)Gaa>Aaa | p.E91K |
SKCM | 7 | 26893780 | 26893780 | + | Splice_Site | SNP | A | A | G | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr7:26893780A>G | c.175T>C | c.(175-177)Tat>Cat | p.Y59H |