| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.69616637C>A | CA261486 | EDA | c.329C>A (p.Ser110Ter) n.571C>A n.552C>A | ClinVar dbSNP |
| X | g.69616637C= | CA2435839596 | EDA | c.329C= (p.Ser110=) n.571C= n.552C= | dbSNP |
| X | g.69616637C>T | CA413447546 | EDA | c.329C>T (p.Ser110Leu) n.571C>T n.552C>T | dbSNP |