D21G (p.Asp21Gly) variant of ARID2 (Q68CP9)
D21G (p.Asp21Gly) in ARID2 (Q68CP9) 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, published literature, and structural context.
D21G (p.Asp21Gly) variant details
- p.Asp21Gly
- gnomAD 12-45729898-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.431
- REVEL 0.35
- MetaLR 0.35
- MetaSVM -0.54
- CADD 27.00
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available