| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.67711549T>C | CA120740 | AR | c.*381T>C (n.*381T>C) c.2033T>C (p.Leu678Pro) c.660T>C (n.660T>C) c.437T>C (p.Leu146Pro) c.1463T>C (p.Leu488Pro) | ClinVar dbSNP |
| X | g.67711549T= | CA2435130481 | AR | c.*381T= (n.*381T=) c.2033T= (p.Leu678=) c.660T= (n.660T=) c.437T= (p.Leu146=) c.1463T= (p.Leu488=) | dbSNP |