| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436843A>G | CA280036 | MAP2K1 | c.323A>G (p.Tyr108Cys) c.389A>G (p.Tyr130Cys) c.291+1606A>G (n.291+1606A>G) n.825A>G n.900A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.66436843A>C | CA392930788 | MAP2K1 | c.323A>C (p.Tyr108Ser) c.389A>C (p.Tyr130Ser) c.291+1606A>C (n.291+1606A>C) n.825A>C n.900A>C | dbSNP |
| 15 | g.66436843A>T | CA392930790 | MAP2K1 | c.323A>T (p.Tyr108Phe) c.389A>T (p.Tyr130Phe) c.291+1606A>T (n.291+1606A>T) n.825A>T n.900A>T | dbSNP |
| 15 | g.66436843A= | CA2184072534 | MAP2K1 | c.323A= (p.Tyr108=) c.389A= (p.Tyr130=) c.291+1606A= (n.291+1606A=) n.825A= n.900A= | dbSNP |