Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.111401108C>A | CA414246047 | DCX | c.587G>T (p.Arg196Leu) c.830G>T (p.Arg277Leu) c.805G>T n.827G>T | ClinVar dbSNP |
X | g.111401108C>T | CA121606 | DCX | c.587G>A (p.Arg196His) c.830G>A (p.Arg277His) c.805G>A n.827G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.111401108C= | CA2451697225 | DCX | c.587G= (p.Arg196=) c.830G= (p.Arg277=) c.805G= n.827G= | dbSNP |