R46P (p.Arg46Pro) variant of CUL3 (Cullin-3)
R46P (p.Arg46Pro) in CUL3 (Cullin-3) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes population frequency data and structural context.
R46P (p.Arg46Pro) variant details
- p.Arg46Pro
- 1000Genomes rs190453078
- ExAC rs190453078
- gnomAD rs190453078
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Population evidence available
- Structural context available