Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435115A>C | CA134595 | MAP2K1 | c.103A>C (p.Lys35Gln) c.169A>C (p.Lys57Gln) n.605A>C n.680A>C | ClinVar dbSNP |
15 | g.66435115A>G | CA16602628 | MAP2K1 | c.103A>G (p.Lys35Glu) c.169A>G (p.Lys57Glu) n.605A>G n.680A>G | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.66435115A= | CA2184071744 | MAP2K1 | c.103A= (p.Lys35=) c.169A= (p.Lys57=) n.605A= n.680A= | dbSNP |