A766S (p.Ala766Ser) variant of AR (Androgen receptor)
A766S (p.Ala766Ser) in AR (Androgen receptor) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Differences in sex development. The record also includes structural context.
A766S (p.Ala766Ser) variant details
- p.Ala766Ser
- gnomAD rs1555996863
- Likely pathogenic
- Differences in sex development
- Missense
- ClinVar: Likely pathogenic (Differences in sex development)
- EBI: Pathogenic (in AIS)
- UniProt: Pathogenic (in AIS)
- Structural context available