| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121515262T>C | CA16618939 | FGFR2 | c.1145A>G (p.Tyr382Cys) c.1142A>G (p.Tyr381Cys) c.-29A>G (n.-29A>G) n.490A>G c.797A>G (p.Tyr266Cys) c.404-11321A>G (n.404-11321A>G) n.3489A>G c.875A>G (p.Tyr292Cys) c.1148A>G (p.Tyr383Cys) c.878A>G (p.Tyr293Cys) c.800A>G (p.Tyr267Cys) c.939+4717A>G (n.939+4717A>G) c.806A>G (p.Tyr269Cys) n.351A>G c.458A>G (p.Tyr153Cys) c.*189A>G (n.*189A>G) n.1592A>G c.1202A>G (p.Tyr401Cys) c.1199A>G (p.Tyr400Cys) c.935A>G (p.Tyr312Cys) c.857A>G (p.Tyr286Cys) c.854A>G (p.Tyr285Cys) c.932A>G (p.Tyr311Cys) n.1578A>G | ClinVar dbSNP |
| 10 | g.121515262T= | CA1941023730 | FGFR2 | c.1145A= (p.Tyr382=) c.1142A= (p.Tyr381=) c.-29A= (n.-29A=) n.490A= c.797A= (p.Tyr266=) c.404-11321A= (n.404-11321A=) n.3489A= c.875A= (p.Tyr292=) c.1148A= (p.Tyr383=) c.878A= (p.Tyr293=) c.800A= (p.Tyr267=) c.939+4717A= (n.939+4717A=) c.806A= (p.Tyr269=) n.351A= c.458A= (p.Tyr153=) c.*189A= (n.*189A=) n.1592A= c.1202A= (p.Tyr401=) c.1199A= (p.Tyr400=) c.935A= (p.Tyr312=) c.857A= (p.Tyr286=) c.854A= (p.Tyr285=) c.932A= (p.Tyr311=) n.1578A= | dbSNP |