C26W (p.Cys26Trp) variant of NOD2 (Q9HC29)
C26W (p.Cys26Trp) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data, published literature, and structural context.
C26W (p.Cys26Trp) variant details
- p.Cys26Trp
- gnomAD 16-50699492-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- MetaLR 0.16
- MetaSVM -0.86
- CADD 22.60
- SIFT 0.09
- Population evidence available
- Structural context available
- Literature evidence available