N39H (p.Asn39His) variant of CUL3 (Cullin-3)
N39H (p.Asn39His) in CUL3 (Cullin-3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
N39H (p.Asn39His) variant details
- p.Asn39His
- rs2469185181
- ClinGen CA351130939
- ClinVar RCV003087072
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available