R26W (p.Arg26Trp) variant of ARID1B (Q8NFD5)
R26W (p.Arg26Trp) in ARID1B (Q8NFD5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
R26W (p.Arg26Trp) variant details
- p.Arg26Trp
- 1000Genomes rs2114952623
- Missense
- Variant Prioritization Score for Impact Estimate 0.253
- CADD 16.90
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available