R10W (p.Arg10Trp) variant of DDX41 (Q9UJV9)
R10W (p.Arg10Trp) in DDX41 (Q9UJV9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
R10W (p.Arg10Trp) variant details
- p.Arg10Trp
- TOPMed rs1161708828
- gnomAD rs1161708828
- Missense
- Variant Prioritization Score for Impact Estimate 0.34
- REVEL 0.17
- CADD 34.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Ashkenazi Jewish population (allele frequency 3.8e-05)
- Structural context available