| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.69616501C>G | CA121312 | EDA | c.193C>G (p.Arg65Gly) n.435C>G n.416C>G | ClinVar dbSNP |
| X | g.69616501C>T | CA413447267 | EDA | c.193C>T (p.Arg65Cys) n.435C>T n.416C>T | dbSNP gnomAD v4 |
| X | g.69616501C= | CA2435839542 | EDA | c.193C= (p.Arg65=) n.435C= n.416C= | dbSNP |