T86N (p.Thr86Asn) variant of PIK3CB (P42338)
T86N (p.Thr86Asn) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data.
T86N (p.Thr86Asn) variant details
- p.Thr86Asn
- gnomAD rs1461410687
- Missense
- Variant Prioritization Score for Impact Estimate 0.701
- CADD 21.20
- PolyPhen-2 0.02
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)