R17W (p.Arg17Trp) variant of CUL3 (Cullin-3)
R17W (p.Arg17Trp) in CUL3 (Cullin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
R17W (p.Arg17Trp) variant details
- p.Arg17Trp
- Ensembl rs866438129
- Missense
- Variant Prioritization Score for Impact Estimate 0.523
- REVEL 0.47
- CADD 30.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available