N36H (p.Asn36His) variant of NOD1 (Q9Y239)
N36H (p.Asn36His) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
N36H (p.Asn36His) variant details
- p.Asn36His
- ExAC rs763163985
- gnomAD rs763163985
- Missense
- Variant Prioritization Score for Impact Estimate 0.277
- REVEL 0.12
- CADD 20.80
- PolyPhen-2 0.10
- SIFT 0.16
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available