| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67723786A>T | CA413428383 | AR | c.*1056A>T (n.*1056A>T) c.2708A>T (p.Gln903Leu) c.1335A>T (n.1335A>T) c.*69A>T (n.*69A>T) c.1112A>T (p.Gln371Leu) c.2159A>T (p.Gln720Leu) | dbSNP |
| X | g.67723786A>G | CA120749 | AR | c.*1056A>G (n.*1056A>G) c.2708A>G (p.Gln903Arg) c.1335A>G (n.1335A>G) c.*69A>G (n.*69A>G) c.1112A>G (p.Gln371Arg) c.2159A>G (p.Gln720Arg) | ClinVar dbSNP COSMIC |