G2W (p.Gly2Trp) variant of NOD2 (Q9HC29)
G2W (p.Gly2Trp) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
G2W (p.Gly2Trp) variant details
- p.Gly2Trp
- gnomAD 16-50697247-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.17
- MetaLR 0.15
- MetaSVM -0.97
- CADD 9.43
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available