A16T (p.Ala16Thr) variant of NOD2 (Q9HC29)
A16T (p.Ala16Thr) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
A16T (p.Ala16Thr) variant details
- p.Ala16Thr
- rs1264322073
- gnomAD 16-50697289-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- MetaLR 0.17
- MetaSVM -0.90
- CADD 11.10
- SIFT 0.26
- Population evidence available
- Structural context available
- Literature evidence available