Y89H (p.Tyr89His) variant of PIK3CB (P42338)
Y89H (p.Tyr89His) 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.
Y89H (p.Tyr89His) variant details
- p.Tyr89His
- gnomAD rs1161845385
- Missense
- Variant Prioritization Score for Impact Estimate 0.585
- CADD 22.40
- PolyPhen-2 0.00
- SIFT 0.47
- Most common in the South Asian population (allele frequency 1.2e-05)