S4G (p.Ser4Gly) variant of PIK3CB (P42338)
S4G (p.Ser4Gly) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data.
S4G (p.Ser4Gly) variant details
- p.Ser4Gly
- cosmic curated COSV10000
- Missense
- Variant Prioritization Score for Impact Estimate 0.174
- CADD 5.90
- PolyPhen-2 0.01
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)