Y89F (p.Tyr89Phe) variant of PIK3CB (P42338)
Y89F (p.Tyr89Phe) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data.
Y89F (p.Tyr89Phe) variant details
- p.Tyr89Phe
- ExAC rs764217455
- TOPMed rs764217455
- gnomAD rs764217455
- Missense
- Variant Prioritization Score for Impact Estimate 0.579
- CADD 22.10
- PolyPhen-2 0.03
- SIFT 0.20
- Most common in the South Asian population (allele frequency 8.1e-05)