| 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 | 6 | 30114921 | 30114921 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr6:30114921C>A | c.601C>A | c.(601-603)Cag>Aag | p.Q201K |
| CESC | 6 | 30105115 | 30105115 | + | Missense_Mutation | SNP | C | C | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr6:30105115C>A | c.302C>A | c.(301-303)tCt>tAt | p.S101Y |
| CESC | 6 | 30114945 | 30114945 | + | Silent | SNP | C | C | T | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr6:30114945C>T | c.625C>T | c.(625-627)Ctg>Ttg | p.L209L |
| CHOL | 6 | 30113806 | 30113806 | + | Missense_Mutation | SNP | G | G | T | TCGA-W5-AA2W-01A-11D-A417-09 | TCGA-W5-AA2W-10A-01D-A41A-09 | g.chr6:30113806G>T | c.381G>T | c.(379-381)aaG>aaT | p.K127N |
| COAD | 6 | 30113786 | 30113786 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr6:30113786C>T | c.361C>T | c.(361-363)Cgg>Tgg | p.R121W |
| COAD | 6 | 30115548 | 30115548 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr6:30115548G>A | c.736G>A | c.(736-738)Gga>Aga | p.G246R |
| COADREAD | 6 | 30113786 | 30113786 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr6:30113786C>T | c.361C>T | c.(361-363)Cgg>Tgg | p.R121W |
| COADREAD | 6 | 30115548 | 30115548 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr6:30115548G>A | c.736G>A | c.(736-738)Gga>Aga | p.G246R |
| GBM | 6 | 30114887 | 30114887 | + | Silent | SNP | G | G | A | TCGA-06-0744-01A-01W-0348-08 | TCGA-06-0744-10A-01W-0348-08 | g.chr6:30114887G>A | c.567G>A | c.(565-567)gcG>gcA | p.A189A |
| GBMLGG | 6 | 30114887 | 30114887 | + | Silent | SNP | G | G | A | TCGA-06-0744-01A-01W-0348-08 | TCGA-06-0744-10A-01W-0348-08 | g.chr6:30114887G>A | c.567G>A | c.(565-567)gcG>gcA | p.A189A |
| GBMLGG | 6 | 30114957 | 30114957 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:30114957G>A | c.637G>A | c.(637-639)Gcc>Acc | p.A213T |
| HNSC | 6 | 30105123 | 30105123 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-6948-01A-11D-1912-08 | TCGA-CV-6948-10A-01D-1912-08 | g.chr6:30105123G>A | c.310G>A | c.(310-312)Gaa>Aaa | p.E104K |
| LGG | 6 | 30114957 | 30114957 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:30114957G>A | c.637G>A | c.(637-639)Gcc>Acc | p.A213T |
| LUAD | 6 | 30104992 | 30104992 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-6851-01A-11D-1945-08 | TCGA-86-6851-10A-01D-1946-08 | g.chr6:30104992G>C | c.179G>C | c.(178-180)tGt>tCt | p.C60S |
| LUAD | 6 | 30105048 | 30105048 | + | Missense_Mutation | SNP | T | T | A | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr6:30105048T>A | c.235T>A | c.(235-237)Tgc>Agc | p.C79S |
| LUAD | 6 | 30113788 | 30113788 | + | Silent | SNP | G | G | A | TCGA-38-4629-01A-02D-1265-08 | TCGA-38-4629-11A-01D-1265-08 | g.chr6:30113788G>A | c.363G>A | c.(361-363)cgG>cgA | p.R121R |
| LUAD | 6 | 30113867 | 30113867 | + | Splice_Site | SNP | G | G | T | TCGA-55-8085-01A-11D-2238-08 | TCGA-55-8085-10A-01D-2238-08 | g.chr6:30113867G>T | | c.e3+1 | |
| LUAD | 6 | 30114911 | 30114911 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr6:30114911G>T | c.591G>T | c.(589-591)agG>agT | p.R197S |
| LUSC | 6 | 30104956 | 30104956 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr6:30104956C>G | c.143C>G | c.(142-144)tCt>tGt | p.S48C |
| LUSC | 6 | 30105078 | 30105078 | + | Silent | SNP | C | C | T | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr6:30105078C>T | c.265C>T | c.(265-267)Cta>Tta | p.L89L |
| OV | 6 | 30115574 | 30115574 | + | Silent | SNP | C | C | G | TCGA-25-1630-01A-01W-0615-10 | TCGA-25-1630-10A-01W-0615-10 | g.chr6:30115574C>G | c.762C>G | c.(760-762)ccC>ccG | p.P254P |
| PAAD | 6 | 30104878 | 30104878 | + | Missense_Mutation | SNP | A | A | G | TCGA-FZ-5926-01A-11D-1609-08 | TCGA-FZ-5926-11A-01D-1609-08 | g.chr6:30104878A>G | c.65A>G | c.(64-66)aAg>aGg | p.K22R |
| PAAD | 6 | 30114887 | 30114887 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:30114887G>A | c.567G>A | c.(565-567)gcG>gcA | p.A189A |
| PRAD | 6 | 30104886 | 30104886 | + | Missense_Mutation | SNP | G | G | A | TCGA-G9-6498-01A-12D-A30X-08 | TCGA-G9-6498-10A-01D-A30X-08 | g.chr6:30104886G>A | c.73G>A | c.(73-75)Gtg>Atg | p.V25M |
| SKCM | 6 | 30104940 | 30104940 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr6:30104940G>A | c.127G>A | c.(127-129)Gag>Aag | p.E43K |
| SKCM | 6 | 30105123 | 30105123 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr6:30105123G>A | c.310G>A | c.(310-312)Gaa>Aaa | p.E104K |
| SKCM | 6 | 30105149 | 30105149 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr6:30105149C>T | c.336C>T | c.(334-336)agC>agT | p.S112S |
| SKCM | 6 | 30114951 | 30114951 | + | Silent | SNP | A | A | C | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr6:30114951A>C | c.631A>C | c.(631-633)Agg>Cgg | p.R211R |
| SKCM | 6 | 30115558 | 30115558 | + | Missense_Mutation | SNP | A | A | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr6:30115558A>C | c.746A>C | c.(745-747)gAa>gCa | p.E249A |