| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121496546A>T | CA16602611 | FGFR2 | c.1852T>A (p.Leu618Met) c.1843T>A (p.Leu615Met) c.673T>A (p.Leu225Met) n.1191T>A c.1498T>A (p.Leu500Met) n.669T>A n.261T>A c.*551T>A (n.*551T>A) n.4190T>A n.2862T>A c.1849T>A (p.Leu617Met) c.1576T>A (p.Leu526Met) c.1582T>A (p.Leu528Met) c.1585T>A (p.Leu529Met) c.1507T>A (p.Leu503Met) c.1501T>A (p.Leu501Met) c.1513T>A (p.Leu505Met) c.625T>A (p.Leu209Met) c.1165T>A (p.Leu389Met) c.*896T>A (n.*896T>A) c.1504T>A (p.Leu502Met) n.2299T>A c.1903T>A (p.Leu635Met) c.1900T>A (p.Leu634Met) c.1909T>A (p.Leu637Met) c.1642T>A (p.Leu548Met) c.1564T>A (p.Leu522Met) c.1906T>A (p.Leu636Met) c.1561T>A (p.Leu521Met) c.1555T>A (p.Leu519Met) c.1639T>A (p.Leu547Met) c.1636T>A (p.Leu546Met) c.1633T>A (p.Leu545Met) c.679T>A (p.Leu227Met) n.2285T>A | ClinVar dbSNP |
| 10 | g.121496546A>C | CA378318835 | FGFR2 | c.1852T>G (p.Leu618Val) c.1843T>G (p.Leu615Val) c.673T>G (p.Leu225Val) n.1191T>G c.1498T>G (p.Leu500Val) n.669T>G n.261T>G c.*551T>G (n.*551T>G) n.4190T>G n.2862T>G c.1849T>G (p.Leu617Val) c.1576T>G (p.Leu526Val) c.1582T>G (p.Leu528Val) c.1585T>G (p.Leu529Val) c.1507T>G (p.Leu503Val) c.1501T>G (p.Leu501Val) c.1513T>G (p.Leu505Val) c.625T>G (p.Leu209Val) c.1165T>G (p.Leu389Val) c.*896T>G (n.*896T>G) c.1504T>G (p.Leu502Val) n.2299T>G c.1903T>G (p.Leu635Val) c.1900T>G (p.Leu634Val) c.1909T>G (p.Leu637Val) c.1642T>G (p.Leu548Val) c.1564T>G (p.Leu522Val) c.1906T>G (p.Leu636Val) c.1561T>G (p.Leu521Val) c.1555T>G (p.Leu519Val) c.1639T>G (p.Leu547Val) c.1636T>G (p.Leu546Val) c.1633T>G (p.Leu545Val) c.679T>G (p.Leu227Val) n.2285T>G | dbSNP |