| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67721837C>T | CA120701 | AR | c.*671C>T (n.*671C>T) c.2323C>T (p.Arg775Cys) c.950C>T (n.950C>T) c.2174-1849C>T (n.2174-1849C>T) c.727C>T (p.Arg243Cys) c.1753C>T (p.Arg585Cys) | ClinVar dbSNP |
| X | g.67721837C>G | CA413426368 | AR | c.*671C>G (n.*671C>G) c.2323C>G (p.Arg775Gly) c.950C>G (n.950C>G) c.2174-1849C>G (n.2174-1849C>G) c.727C>G (p.Arg243Gly) c.1753C>G (p.Arg585Gly) | dbSNP |