P107R (p.Pro107Arg) variant of PIK3CB (P42338)
P107R (p.Pro107Arg) 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 and structural context.
P107R (p.Pro107Arg) variant details
- p.Pro107Arg
- gnomAD rs1219491121
- Missense
- Variant Prioritization Score for Impact Estimate 0.78
- CADD 27.00
- PolyPhen-2 0.97
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available