R10G (p.Arg10Gly) variant of DDX41 (Q9UJV9)
R10G (p.Arg10Gly) in DDX41 (Q9UJV9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
R10G (p.Arg10Gly) variant details
- p.Arg10Gly
- TOPMed rs1161708828
- gnomAD rs1161708828
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- REVEL 0.14
- CADD 33.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available