N26S (p.Asn26Ser) variant of NOD1 (Q9Y239)
N26S (p.Asn26Ser) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
N26S (p.Asn26Ser) variant details
- p.Asn26Ser
- 1000Genomes rs181282889
- ExAC rs181282889
- TOPMed rs181282889
- gnomAD rs181282889
- Missense
- Variant Prioritization Score for Impact Estimate 0.0963
- REVEL 0.05
- CADD 13.90
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available