L39P (p.Leu39Pro) variant of WAS (P42768)
L39P (p.Leu39Pro) in WAS (P42768) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
L39P (p.Leu39Pro) variant details
- p.Leu39Pro
- gnomAD rs1557006245
- Missense
- Variant Prioritization Score for Impact Estimate 0.768
- REVEL 0.90
- CADD 28.10
- PolyPhen-2 0.72
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available