| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436809C>G | CA392930601 | MAP2K1 | c.289C>G (p.His97Asp) c.355C>G (p.His119Asp) c.291+1572C>G (n.291+1572C>G) n.791C>G n.866C>G | dbSNP |
| 15 | g.66436809C>A | CA392930600 | MAP2K1 | c.289C>A (p.His97Asn) c.355C>A (p.His119Asn) c.291+1572C>A (n.291+1572C>A) n.791C>A n.866C>A | dbSNP |
| 15 | g.66436809C>T | CA296112 | MAP2K1 | c.289C>T (p.His97Tyr) c.355C>T (p.His119Tyr) c.291+1572C>T (n.291+1572C>T) n.791C>T n.866C>T | ClinVar dbSNP COSMIC |
| 15 | g.66436809C= | CA2184072512 | MAP2K1 | c.289C= (p.His97=) c.355C= (p.His119=) c.291+1572C= (n.291+1572C=) n.791C= n.866C= | dbSNP |