H19D (p.His19Asp) variant of NOD1 (Q9Y239)
H19D (p.His19Asp) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
H19D (p.His19Asp) variant details
- p.His19Asp
- ExAC rs768207776
- gnomAD rs768207776
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- REVEL 0.21
- CADD 1.73
- PolyPhen-2 0.06
- SIFT 0.12
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available