| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436842T>C | CA279999 | MAP2K1 | c.322T>C (p.Tyr108His) c.388T>C (p.Tyr130His) c.291+1605T>C (n.291+1605T>C) n.824T>C n.899T>C | ClinVar dbSNP |
| 15 | g.66436842T>A | CA392930783 | MAP2K1 | c.322T>A (p.Tyr108Asn) c.388T>A (p.Tyr130Asn) c.291+1605T>A (n.291+1605T>A) n.824T>A n.899T>A | ClinVar dbSNP |