| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723688T>A | CA413428141 | AR | c.*958T>A (n.*958T>A) c.2610T>A (p.Ile870=) c.1237T>A (n.1237T>A) c.2176T>A (p.Cys726Ser) c.1014T>A (p.Ile338=) c.2061T>A (p.Ile687=) | dbSNP |
| X | g.67723688T>G | CA120723 | AR | c.*958T>G (n.*958T>G) c.2610T>G (p.Ile870Met) c.1237T>G (n.1237T>G) c.2176T>G (p.Cys726Gly) c.1014T>G (p.Ile338Met) c.2061T>G (p.Ile687Met) | ClinVar dbSNP |