R17G (p.Arg17Gly) variant of ARID1B (Q8NFD5)
R17G (p.Arg17Gly) in ARID1B (Q8NFD5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
R17G (p.Arg17Gly) variant details
- p.Arg17Gly
- gnomAD 6-156777729-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.28
- CADD 14.20
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available