| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67711468del | CA16621464 | AR | c.*300del (n.*300del) c.1952del (p.Ser651ThrfsTer10) c.579del (n.579del) c.356del (p.Ser119ThrfsTer10) c.1382del (p.Ser461ThrfsTer10) | ClinVar dbSNP |
| X | g.67711468G= | CA3065189126 | AR | c.*300G= (n.*300G=) c.1952G= (p.Ser651=) c.579G= (n.579G=) c.356G= (p.Ser119=) c.1382G= (p.Ser461=) | dbSNP |