P18H (p.Pro18His) variant of NOD1 (Q9Y239)
P18H (p.Pro18His) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
P18H (p.Pro18His) variant details
- p.Pro18His
- ExAC rs747367948
- gnomAD rs747367948
- Missense
- Variant Prioritization Score for Impact Estimate 0.29
- REVEL 0.15
- CADD 19.80
- PolyPhen-2 0.12
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available