| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436810A>T | CA392930607 | MAP2K1 | c.290A>T (p.His97Leu) c.356A>T (p.His119Leu) c.291+1573A>T (n.291+1573A>T) n.792A>T n.867A>T | dbSNP |
| 15 | g.66436810A>G | CA392930606 | MAP2K1 | c.290A>G (p.His97Arg) c.356A>G (p.His119Arg) c.291+1573A>G (n.291+1573A>G) n.792A>G n.867A>G | dbSNP |
| 15 | g.66436810A>C | CA16602650 | MAP2K1 | c.290A>C (p.His97Pro) c.356A>C (p.His119Pro) c.291+1573A>C (n.291+1573A>C) n.792A>C n.867A>C | ClinVar dbSNP |