| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.70035394G>T | CA261512 | EDA | c.961G>T (p.Glu321Ter) c.955G>T (p.Glu319Ter) c.946G>T (p.Glu316Ter) c.565G>T (p.Glu189Ter) c.952G>T (p.Glu318Ter) c.919G>T (p.Glu307Ter) | ClinVar dbSNP |
| X | g.70035394G>A | CA413449469 | EDA | c.961G>A (p.Glu321Lys) c.955G>A (p.Glu319Lys) c.946G>A (p.Glu316Lys) c.565G>A (p.Glu189Lys) c.952G>A (p.Glu318Lys) c.919G>A (p.Glu307Lys) | ClinVar dbSNP |