Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435070C>T | CA279993 | MAP2K1 | c.58C>T (p.Leu20Phe) c.124C>T (p.Leu42Phe) n.560C>T n.635C>T | ClinVar dbSNP COSMIC |
15 | g.66435070C>G | CA392929043 | MAP2K1 | c.58C>G (p.Leu20Val) c.124C>G (p.Leu42Val) n.560C>G n.635C>G | dbSNP |
15 | g.66435070C= | CA2184071719 | MAP2K1 | c.58C= (p.Leu20=) c.124C= (p.Leu42=) n.560C= n.635C= | dbSNP |