C39R (p.Cys39Arg) variant of NOD1 (Q9Y239)
C39R (p.Cys39Arg) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
C39R (p.Cys39Arg) variant details
- p.Cys39Arg
- 1000Genomes rs550336227
- ExAC rs550336227
- TOPMed rs550336227
- gnomAD rs550336227
- Missense
- Variant Prioritization Score for Impact Estimate 0.604
- REVEL 0.57
- CADD 27.00
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available