| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.69616489T>A | CA413447243 | EDA | c.181T>A (p.Tyr61Asn) n.423T>A n.404T>A | ClinVar dbSNP |
| X | g.69616489T>C | CA255649 | EDA | c.181T>C (p.Tyr61His) n.423T>C n.404T>C | ClinVar dbSNP |
| X | g.69616489T= | CA2435839539 | EDA | c.181T= (p.Tyr61=) n.423T= n.404T= | dbSNP |