| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116777409C>T | CA16602530 | MET | c.*885C>T (n.*885C>T) c.3334C>T (p.His1112Tyr) c.3280C>T (p.His1094Tyr) c.1990C>T (p.His664Tyr) c.3337C>T (p.His1113Tyr) n.3411C>T | ClinVar dbSNP COSMIC |
| 7 | g.116777409C>G | CA368989595 | MET | c.*885C>G (n.*885C>G) c.3334C>G (p.His1112Asp) c.3280C>G (p.His1094Asp) c.1990C>G (p.His664Asp) c.3337C>G (p.His1113Asp) n.3411C>G | dbSNP |