A16G (p.Ala16Gly) variant of NOD2 (Q9HC29)
A16G (p.Ala16Gly) in NOD2 (Q9HC29) 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, published literature, and structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- gnomAD 16-50697290-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- MetaLR 0.15
- MetaSVM -0.88
- CADD 7.22
- SIFT 0.37
- Population evidence available
- Structural context available
- Literature evidence available