| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116782048C>T | CA10584670 | MET | c.*1188C>T (n.*1188C>T) c.3637C>T (p.Leu1213Phe) c.3583C>T (p.Leu1195Phe) c.2293C>T (p.Leu765Phe) c.3640C>T (p.Leu1214Phe) n.3714C>T | ClinVar dbSNP COSMIC |
| 7 | g.116782048C>A | CA368991080 | MET | c.*1188C>A (n.*1188C>A) c.3637C>A (p.Leu1213Ile) c.3583C>A (p.Leu1195Ile) c.2293C>A (p.Leu765Ile) c.3640C>A (p.Leu1214Ile) n.3714C>A | dbSNP COSMIC |
| 7 | g.116782048C>G | CA257006 | MET | c.*1188C>G (n.*1188C>G) c.3637C>G (p.Leu1213Val) c.3583C>G (p.Leu1195Val) c.2293C>G (p.Leu765Val) c.3640C>G (p.Leu1214Val) n.3714C>G | ClinVar dbSNP COSMIC |