| 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 |
|---|
| ACC | 17 | 35734873 | 35734873 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5L2-01A-11D-A30A-10 | TCGA-OR-A5L2-10A-01D-A30A-10 | g.chr17:35734873G>A | c.115G>A | c.(115-117)Gtg>Atg | p.V39M |
| BRCA | 17 | 35736110 | 35736110 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AO-A03N-01B-11D-A10M-09 | TCGA-AO-A03N-10A-01D-A10M-09 | g.chr17:35736110C>T | c.181C>T | c.(181-183)Caa>Taa | p.Q61* |
| CHOL | 17 | 35746204 | 35746204 | + | Missense_Mutation | SNP | G | G | T | TCGA-W5-AA2G-01A-11D-A417-09 | TCGA-W5-AA2G-10A-01D-A41A-09 | g.chr17:35746204G>T | c.657G>T | c.(655-657)aaG>aaT | p.K219N |
| CHOL | 17 | 35746210 | 35746210 | + | Silent | SNP | C | C | T | TCGA-W5-AA2X-01A-11D-A417-09 | TCGA-W5-AA2X-10A-01D-A41A-09 | g.chr17:35746210C>T | c.663C>T | c.(661-663)tgC>tgT | p.C221C |
| COAD | 17 | 35734837 | 35734837 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A01P-01A-21W-A096-10 | TCGA-AA-A01P-11A-11W-A096-10 | g.chr17:35734837C>T | c.79C>T | c.(79-81)Cga>Tga | p.R27* |
| COAD | 17 | 35736152 | 35736152 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:35736152A>G | c.223A>G | c.(223-225)Agc>Ggc | p.S75G |
| COAD | 17 | 35736170 | 35736170 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:35736170C>A | c.241C>A | c.(241-243)Ctt>Att | p.L81I |
| COAD | 17 | 35736291 | 35736291 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr17:35736291T>C | c.362T>C | c.(361-363)tTt>tCt | p.F121S |
| COAD | 17 | 35742958 | 35742958 | + | Missense_Mutation | SNP | G | G | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr17:35742958G>T | c.403G>T | c.(403-405)Ggg>Tgg | p.G135W |
| COAD | 17 | 35743037 | 35743039 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr17:35743037_35743039delAAG | c.482_484delAAG | c.(481-486)aaagaa>aaa | p.E162del |
| COADREAD | 17 | 35734837 | 35734837 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A01P-01A-21W-A096-10 | TCGA-AA-A01P-11A-11W-A096-10 | g.chr17:35734837C>T | c.79C>T | c.(79-81)Cga>Tga | p.R27* |
| COADREAD | 17 | 35736152 | 35736152 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:35736152A>G | c.223A>G | c.(223-225)Agc>Ggc | p.S75G |
| COADREAD | 17 | 35736170 | 35736170 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:35736170C>A | c.241C>A | c.(241-243)Ctt>Att | p.L81I |
| COADREAD | 17 | 35736291 | 35736291 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr17:35736291T>C | c.362T>C | c.(361-363)tTt>tCt | p.F121S |
| COADREAD | 17 | 35742958 | 35742958 | + | Missense_Mutation | SNP | G | G | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr17:35742958G>T | c.403G>T | c.(403-405)Ggg>Tgg | p.G135W |
| COADREAD | 17 | 35743037 | 35743039 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr17:35743037_35743039delAAG | c.482_484delAAG | c.(481-486)aaagaa>aaa | p.E162del |
| ESCA | 17 | 35736300 | 35736300 | + | Missense_Mutation | SNP | G | G | C | TCGA-VR-AA7I-01A-11D-A403-09 | TCGA-VR-AA7I-10A-01D-A403-09 | g.chr17:35736300G>C | c.371G>C | c.(370-372)gGa>gCa | p.G124A |
| ESCA | 17 | 35746184 | 35746184 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IG-A3Y9-01A-12D-A247-09 | TCGA-IG-A3Y9-10A-01D-A247-09 | g.chr17:35746184C>T | c.637C>T | c.(637-639)Caa>Taa | p.Q213* |
| GBMLGG | 17 | 35733066 | 35733066 | + | Missense_Mutation | SNP | T | T | C | TCGA-TQ-A7RW-01A-11D-A33T-08 | TCGA-TQ-A7RW-10A-01D-A33W-08 | g.chr17:35733066T>C | c.32T>C | c.(31-33)aTt>aCt | p.I11T |
| LGG | 17 | 35733066 | 35733066 | + | Missense_Mutation | SNP | T | T | C | TCGA-TQ-A7RW-01A-11D-A33T-08 | TCGA-TQ-A7RW-10A-01D-A33W-08 | g.chr17:35733066T>C | c.32T>C | c.(31-33)aTt>aCt | p.I11T |
| LIHC | 17 | 35736083 | 35736083 | + | Missense_Mutation | SNP | A | A | G | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr17:35736083A>G | c.154A>G | c.(154-156)Aca>Gca | p.T52A |
| LUAD | 17 | 35733069 | 35733069 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7765-01A-11D-2167-08 | TCGA-69-7765-10A-01D-2167-08 | g.chr17:35733069C>A | c.35C>A | c.(34-36)gCa>gAa | p.A12E |
| LUAD | 17 | 35733081 | 35733081 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-8640-01A-11D-2393-08 | TCGA-78-8640-11A-01D-2393-08 | g.chr17:35733081C>A | c.47C>A | c.(46-48)gCc>gAc | p.A16D |
| LUAD | 17 | 35734819 | 35734819 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr17:35734819C>A | c.61C>A | c.(61-63)Ctc>Atc | p.L21I |
| LUAD | 17 | 35734843 | 35734843 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr17:35734843G>C | c.85G>C | c.(85-87)Gaa>Caa | p.E29Q |
| LUAD | 17 | 35742976 | 35742976 | + | Missense_Mutation | SNP | G | G | C | TCGA-35-4123-01A-01D-1105-08 | TCGA-35-4123-10A-01D-1105-08 | g.chr17:35742976G>C | c.421G>C | c.(421-423)Gtc>Ctc | p.V141L |
| LUAD | 17 | 35745728 | 35745728 | + | Splice_Site | SNP | C | C | A | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr17:35745728C>A | c.632C>A | c.(631-633)cCt>cAt | p.P211H |
| PRAD | 17 | 35736258 | 35736258 | + | Missense_Mutation | SNP | C | C | G | TCGA-EJ-7123-01A-11D-1961-08 | TCGA-EJ-7123-10A-01D-1961-08 | g.chr17:35736258C>G | c.329C>G | c.(328-330)tCc>tGc | p.S110C |
| PRAD | 17 | 35745662 | 35745662 | + | Missense_Mutation | SNP | T | T | A | TCGA-HI-7171-01A-12D-2114-08 | TCGA-HI-7171-10A-01D-2115-08 | g.chr17:35745662T>A | c.566T>A | c.(565-567)aTt>aAt | p.I189N |
| SKCM | 17 | 35736186 | 35736186 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr17:35736186G>A | c.257G>A | c.(256-258)aGa>aAa | p.R86K |
| SKCM | 17 | 35736299 | 35736299 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr17:35736299G>A | c.370G>A | c.(370-372)Gga>Aga | p.G124R |
| SKCM | 17 | 35743032 | 35743032 | + | Silent | SNP | G | G | A | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr17:35743032G>A | c.477G>A | c.(475-477)ggG>ggA | p.G159G |
| SKCM | 17 | 35745681 | 35745681 | + | Silent | SNP | C | C | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr17:35745681C>A | c.585C>A | c.(583-585)ctC>ctA | p.L195L |