R4W (p.Arg4Trp) variant of ARID1B (Q8NFD5)
R4W (p.Arg4Trp) in ARID1B (Q8NFD5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
R4W (p.Arg4Trp) variant details
- p.Arg4Trp
- gnomAD rs1401179920
- Missense
- Variant Prioritization Score for Impact Estimate 0.433
- CADD 17.50
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Structural context available