| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.69616491C>T | CA517051650 | EDA | c.183C>T (p.Tyr61=) n.425C>T n.406C>T | ClinVar dbSNP gnomAD v4 |
| X | g.69616491C>G | CA255658 | EDA | c.183C>G (p.Tyr61Ter) n.425C>G n.406C>G | ClinVar dbSNP |
| X | g.69616491C= | CA2435839540 | EDA | c.183C= (p.Tyr61=) n.425C= n.406C= | dbSNP |