| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723728A>T | CA120698 | AR | c.*998A>T (n.*998A>T) c.2650A>T (p.Lys884Ter) c.1277A>T (n.1277A>T) c.*11A>T (n.*11A>T) c.1054A>T (p.Lys352Ter) c.2101A>T (p.Lys701Ter) | ClinVar dbSNP |
| X | g.67723728A= | CA2435134804 | AR | c.*998A= (n.*998A=) c.2650A= (p.Lys884=) c.1277A= (n.1277A=) c.*11A= (n.*11A=) c.1054A= (p.Lys352=) c.2101A= (p.Lys701=) | dbSNP |