G89S (p.Gly89Ser) variant of WAS (P42768)
G89S (p.Gly89Ser) in WAS (P42768) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
G89S (p.Gly89Ser) variant details
- p.Gly89Ser
- ExAC rs782405509
- TOPMed rs782405509
- gnomAD rs782405509
- Missense
- Variant Prioritization Score for Impact Estimate 0.511
- REVEL 0.48
- CADD 17.10
- PolyPhen-2 0.03
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 1.7e-05)
- Structural context available