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 |
7 | g.116783402A= | CA1737014532 | MET | c.*1336A= (n.*1336A=) c.3785A= (p.Lys1262=) c.3731A= (p.Lys1244=) c.2441A= (p.Lys814=) c.3788A= (p.Lys1263=) n.3862A= | dbSNP |