P9S (p.Pro9Ser) variant of PIK3CB (P42338)
P9S (p.Pro9Ser) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data.
P9S (p.Pro9Ser) variant details
- p.Pro9Ser
- cosmic curated COSV56685
- Missense
- Variant Prioritization Score for Impact Estimate 0.785
- CADD 26.20
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)