| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436750T>A | CA392930191 | MAP2K1 | c.230T>A (p.Ile77Asn) c.296T>A (p.Ile99Asn) c.291+1513T>A (n.291+1513T>A) n.732T>A n.807T>A | dbSNP |
| 15 | g.66436750T>C | CA16602647 | MAP2K1 | c.230T>C (p.Ile77Thr) c.296T>C (p.Ile99Thr) c.291+1513T>C (n.291+1513T>C) n.732T>C n.807T>C | ClinVar dbSNP |