D74G (p.Asp74Gly) variant of PIK3CB (P42338)
D74G (p.Asp74Gly) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data.
D74G (p.Asp74Gly) variant details
- p.Asp74Gly
- ExAC rs757588885
- TOPMed rs757588885
- gnomAD rs757588885
- Missense
- Variant Prioritization Score for Impact Estimate 0.592
- CADD 23.70
- PolyPhen-2 0.11
- SIFT 0.10
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)