P38S (p.Pro38Ser) variant of DDX41 (Q9UJV9)
P38S (p.Pro38Ser) in DDX41 (Q9UJV9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- gnomAD rs1406601195
- Missense
- Variant Prioritization Score for Impact Estimate 0.478
- REVEL 0.25
- CADD 26.70
- PolyPhen-2 1.00
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available