Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.70033426G>A | CA273144 | EDA | c.822G>A (p.Trp274Ter) c.813G>A (p.Trp271Ter) c.426G>A (p.Trp142Ter) | ClinVar dbSNP |
X | g.70033426G>T | CA261505 | EDA | c.822G>T (p.Trp274Cys) c.813G>T (p.Trp271Cys) c.426G>T (p.Trp142Cys) | ClinVar dbSNP |
X | g.70033426G= | CA2435981292 | EDA | c.822G= (p.Trp274=) c.813G= (p.Trp271=) c.426G= (p.Trp142=) | dbSNP |