| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67643387T>A | CA120761 | AR | c.*96T>A (n.*96T>A) c.1748T>A (p.Phe583Tyr) c.375T>A (n.375T>A) c.152T>A (p.Phe51Tyr) n.2075T>A c.1178T>A (p.Phe393Tyr) c.1617-42554T>A (n.1617-42554T>A) | ClinVar dbSNP |
| X | g.67643387T= | CA2435101978 | AR | c.*96T= (n.*96T=) c.1748T= (p.Phe583=) c.375T= (n.375T=) c.152T= (p.Phe51=) n.2075T= c.1178T= (p.Phe393=) c.1617-42554T= (n.1617-42554T=) | dbSNP |