S17T (p.Ser17Thr) variant of NOD2 (Q9HC29)
S17T (p.Ser17Thr) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
S17T (p.Ser17Thr) variant details
- p.Ser17Thr
- gnomAD 16-50697293-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- MetaLR 0.12
- MetaSVM -0.98
- CADD 0.56
- SIFT 0.25
- Population evidence available
- Structural context available
- Literature evidence available