D11G (p.Asp11Gly) variant of NOD2 (Q9HC29)
D11G (p.Asp11Gly) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
D11G (p.Asp11Gly) variant details
- p.Asp11Gly
- gnomAD 16-50697275-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.128
- MetaLR 0.16
- MetaSVM -0.93
- CADD 0.17
- SIFT 0.41
- Population evidence available
- Structural context available
- Literature evidence available