| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.70035505C>G | CA121313 | EDA | c.1072C>G (p.Gln358Glu) c.1066C>G (p.Gln356Glu) c.1057C>G (p.Gln353Glu) c.676C>G (p.Gln226Glu) c.1063C>G (p.Gln355Glu) c.1030C>G (p.Gln344Glu) | ClinVar dbSNP |
| X | g.70035505C= | CA2435981949 | EDA | c.1072C= (p.Gln358=) c.1066C= (p.Gln356=) c.1057C= (p.Gln353=) c.676C= (p.Gln226=) c.1063C= (p.Gln355=) c.1030C= (p.Gln344=) | dbSNP |