I17N (p.Ile17Asn) variant of PIK3CB (P42338)
I17N (p.Ile17Asn) in PIK3CB (P42338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data.
I17N (p.Ile17Asn) variant details
- p.Ile17Asn
- ExAC rs763276798
- gnomAD rs763276798
- Missense
- Variant Prioritization Score for Impact Estimate 0.497
- CADD 24.00
- PolyPhen-2 0.01
- SIFT 0.01
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)