Q91H (p.Gln91His) variant of NOD1 (Q9Y239)
Q91H (p.Gln91His) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
Q91H (p.Gln91His) variant details
- p.Gln91His
- gnomAD rs1435507974
- Missense
- Variant Prioritization Score for Impact Estimate 0.208
- REVEL 0.07
- CADD 17.00
- PolyPhen-2 0.13
- SIFT 0.14
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available