R98T (p.Arg98Thr) variant of PIK3CB (P42338)
R98T (p.Arg98Thr) 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.
R98T (p.Arg98Thr) variant details
- p.Arg98Thr
- Ensembl rs2108721657
- Missense
- Variant Prioritization Score for Impact Estimate 0.779
- CADD 26.30
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)