| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.4110586A>C | CA403391522 | MAP2K2 | n.812T>G c.373T>G (p.Cys125Gly) c.82T>G (p.Cys28Gly) n.570T>G | dbSNP |
| 19 | g.4110586A>T | CA16602632 | MAP2K2 | n.812T>A c.373T>A (p.Cys125Ser) c.82T>A (p.Cys28Ser) n.570T>A | ClinVar dbSNP COSMIC COSMIC |