Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.111410173G>C | CA414246842 | DCX | c.226C>G (p.Arg76Gly) c.469C>G (p.Arg157Gly) c.444C>G n.466C>G | ClinVar dbSNP |
X | g.111410173G>A | CA171890 | DCX | c.226C>T (p.Arg76Cys) c.469C>T (p.Arg157Cys) c.444C>T n.466C>T | ClinVar dbSNP |
X | g.111410173G>T | CA414246843 | DCX | c.226C>A (p.Arg76Ser) c.469C>A (p.Arg157Ser) c.444C>A n.466C>A | dbSNP gnomAD v2 gnomAD v4 |