| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116778827T>A | CA368990052 | MET | c.*997T>A (n.*997T>A) c.3446T>A (p.Met1149Lys) c.3392T>A (p.Met1131Lys) c.2102T>A (p.Met701Lys) c.3449T>A (p.Met1150Lys) n.3523T>A | dbSNP |
| 7 | g.116778827T>C | CA256991 | MET | c.*997T>C (n.*997T>C) c.3446T>C (p.Met1149Thr) c.3392T>C (p.Met1131Thr) c.2102T>C (p.Met701Thr) c.3449T>C (p.Met1150Thr) n.3523T>C | ClinVar dbSNP COSMIC |