| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.111401028C>T | CA172046 | DCX | c.667G>A (p.Gly223Arg) c.910G>A (p.Gly304Arg) c.885G>A n.907G>A | ClinVar dbSNP gnomAD v2 |
| X | g.111401028C>G | CA16621176 | DCX | c.667G>C (p.Gly223Arg) c.910G>C (p.Gly304Arg) c.885G>C n.907G>C | ClinVar dbSNP |
| X | g.111401028C= | CA2451697206 | DCX | c.667G= (p.Gly223=) c.910G= (p.Gly304=) c.885G= n.907G= | dbSNP |