C69G (p.Cys69Gly) variant of WAS (P42768)
C69G (p.Cys69Gly) in WAS (P42768) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
C69G (p.Cys69Gly) variant details
- p.Cys69Gly
- TOPMed rs1156735272
- gnomAD rs1156735272
- Missense
- Variant Prioritization Score for Impact Estimate 0.515
- REVEL 0.59
- CADD 24.70
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available