| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116763206T>A | CA368983514 | MET | c.2521T>A (p.Phe841Ile) c.*126T>A (n.*126T>A) c.2575T>A (p.Phe859Ile) c.361T>A (p.Phe121Ile) c.1231T>A (p.Phe411Ile) c.2578T>A (p.Phe860Ile) n.2652T>A | dbSNP |
| 7 | g.116763206T>G | CA212644 | MET | c.2521T>G (p.Phe841Val) c.*126T>G (n.*126T>G) c.2575T>G (p.Phe859Val) c.361T>G (p.Phe121Val) c.1231T>G (p.Phe411Val) c.2578T>G (p.Phe860Val) n.2652T>G | ClinVar dbSNP |
| 7 | g.116763206T= | CA1737029662 | MET | c.2521T= (p.Phe841=) c.*126T= (n.*126T=) c.2575T= (p.Phe859=) c.361T= (p.Phe121=) c.1231T= (p.Phe411=) c.2578T= (p.Phe860=) n.2652T= | dbSNP |