V18V (p.Val18Val) variant of WAS (P42768)
V18V (p.Val18Val) in WAS (P42768) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
V18V (p.Val18Val) variant details
- p.Val18Val
- gnomAD X-48683907-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.278
- CADD 5.25
- Most common in the Non-Finnish European population (allele frequency 0.00027)
- Structural context available
- Literature evidence available