P37S (p.Pro37Ser) variant of PIK3CB (P42338)
P37S (p.Pro37Ser) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- Ensembl rs2108733904
- Missense
- Variant Prioritization Score for Impact Estimate 0.772
- CADD 25.50
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)