R20Q (p.Arg20Gln) variant of AR (Androgen receptor)
R20Q (p.Arg20Gln) in AR (Androgen receptor) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes experimental measurements and structural context.
R20Q (p.Arg20Gln) variant details
- p.Arg20Gln
- TOPMed rs1297947716
- gnomAD rs1297947716
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available
- AR Zinc finger, nuclear hormone receptor-type domain domainome 1.0: score -0.637