| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436839T>C | CA16602630 | MAP2K1 | c.319T>C (p.Phe107Leu) c.385T>C (p.Phe129Leu) c.291+1602T>C (n.291+1602T>C) n.821T>C n.896T>C | ClinVar ClinVar dbSNP |
| 15 | g.66436839T>A | CA392930768 | MAP2K1 | c.319T>A (p.Phe107Ile) c.385T>A (p.Phe129Ile) c.291+1602T>A (n.291+1602T>A) n.821T>A n.896T>A | dbSNP |