Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.111410095G>A | CA171923 | DCX | c.304C>T (p.Arg102Cys) c.547C>T (p.Arg183Cys) c.522C>T n.544C>T | ClinVar dbSNP COSMIC COSMIC |
X | g.111410095G>C | CA10603581 | DCX | c.304C>G (p.Arg102Gly) c.547C>G (p.Arg183Gly) c.522C>G n.544C>G | ClinVar dbSNP |
X | g.111410095G>T | CA414246685 | DCX | c.304C>A (p.Arg102Ser) c.547C>A (p.Arg183Ser) c.522C>A n.544C>A | ClinVar dbSNP |