| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174771A>G | CA16602542 | EGFR | c.2075A>G (p.Lys692Arg) c.583A>G c.2234A>G (p.Lys745Arg) c.*28+1843A>G (n.*28+1843A>G) c.2099A>G (p.Lys700Arg) c.1433A>G (p.Lys478Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55174771A= | CA1708918312 | EGFR | c.2075A= (p.Lys692=) c.583A= c.2234A= (p.Lys745=) c.*28+1843A= (n.*28+1843A=) c.2099A= (p.Lys700=) c.1433A= (p.Lys478=) | dbSNP |