| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116783402A>T | CA368991791 | MET | c.*1336A>T (n.*1336A>T) c.3785A>T (p.Lys1262Met) c.3731A>T (p.Lys1244Met) c.2441A>T (p.Lys814Met) c.3788A>T (p.Lys1263Met) n.3862A>T | dbSNP |
| 7 | g.116783402A>C | CA368991796 | MET | c.*1336A>C (n.*1336A>C) c.3785A>C (p.Lys1262Thr) c.3731A>C (p.Lys1244Thr) c.2441A>C (p.Lys814Thr) c.3788A>C (p.Lys1263Thr) n.3862A>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.116783402A>G | CA123614 | MET | c.*1336A>G (n.*1336A>G) c.3785A>G (p.Lys1262Arg) c.3731A>G (p.Lys1244Arg) c.2441A>G (p.Lys814Arg) c.3788A>G (p.Lys1263Arg) n.3862A>G | ClinVar dbSNP COSMIC |