| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67711585A>T | CA413423343 | AR | c.*417A>T (n.*417A>T) c.2069A>T (p.His690Leu) c.696A>T (n.696A>T) c.473A>T (p.His158Leu) c.1499A>T (p.His500Leu) | dbSNP |
| X | g.67711585A>C | CA120783 | AR | c.*417A>C (n.*417A>C) c.2069A>C (p.His690Pro) c.696A>C (n.696A>C) c.473A>C (p.His158Pro) c.1499A>C (p.His500Pro) | ClinVar dbSNP |
| X | g.67711585A>G | CA413423342 | AR | c.*417A>G (n.*417A>G) c.2069A>G (p.His690Arg) c.696A>G (n.696A>G) c.473A>G (p.His158Arg) c.1499A>G (p.His500Arg) | dbSNP |
| X | g.67711585A= | CA2435130494 | AR | c.*417A= (n.*417A=) c.2069A= (p.His690=) c.696A= (n.696A=) c.473A= (p.His158=) c.1499A= (p.His500=) | dbSNP |