A92D (p.Ala92Asp) variant of WAS (P42768)
A92D (p.Ala92Asp) in WAS (P42768) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
A92D (p.Ala92Asp) variant details
- p.Ala92Asp
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.439
- REVEL 0.45
- CADD 17.00
- PolyPhen-2 0.05
- SIFT 0.57
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available