P78Q (p.Pro78Gln) variant of DDX41 (Q9UJV9)
P78Q (p.Pro78Gln) in DDX41 (Q9UJV9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
P78Q (p.Pro78Gln) variant details
- p.Pro78Gln
- ExAC rs766355942
- gnomAD rs766355942
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.13
- CADD 22.00
- PolyPhen-2 0.03
- SIFT 0.43
- Most common in the South Asian population (allele frequency 5.8e-05)
- Structural context available