E13G (p.Glu13Gly) variant of NOD2 (Q9HC29)
E13G (p.Glu13Gly) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
E13G (p.Glu13Gly) variant details
- p.Glu13Gly
- gnomAD 16-50697281-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- MetaLR 0.15
- MetaSVM -0.97
- CADD 10.50
- SIFT 0.09
- Population evidence available
- Structural context available
- Literature evidence available