S77R (p.Ser77Arg) variant of NOD1 (Q9Y239)
S77R (p.Ser77Arg) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
S77R (p.Ser77Arg) variant details
- p.Ser77Arg
- ExAC rs751982098
- TOPMed rs751982098
- gnomAD rs751982098
- Missense
- Variant Prioritization Score for Impact Estimate 0.355
- REVEL 0.18
- CADD 23.90
- PolyPhen-2 0.99
- SIFT 0.07
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available