S9T (p.Ser9Thr) variant of NOD2 (Q9HC29)
S9T (p.Ser9Thr) 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.
S9T (p.Ser9Thr) variant details
- p.Ser9Thr
- gnomAD 16-50697268-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- MetaLR 0.15
- MetaSVM -0.92
- CADD 1.58
- SIFT 0.85
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available
- Literature evidence available