Y88C (p.Tyr88Cys) variant of NOD1 (Q9Y239)
Y88C (p.Tyr88Cys) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
Y88C (p.Tyr88Cys) variant details
- p.Tyr88Cys
- TOPMed rs780605529
- gnomAD rs780605529
- Missense
- Variant Prioritization Score for Impact Estimate 0.234
- REVEL 0.06
- CADD 21.10
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available