I17V (p.Ile17Val) variant of PIK3CB (P42338)
I17V (p.Ile17Val) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data.
I17V (p.Ile17Val) variant details
- p.Ile17Val
- TOPMed rs1172688851
- Missense
- Variant Prioritization Score for Impact Estimate 0.558
- CADD 18.20
- PolyPhen-2 0.01
- SIFT 0.50
- Most common in the Non-Finnish European population (allele frequency 9e-07)