D66N (p.Asp66Asn) variant of NOD1 (Q9Y239)
D66N (p.Asp66Asn) 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.
D66N (p.Asp66Asn) variant details
- p.Asp66Asn
- TOPMed rs1786414423
- gnomAD rs1786414423
- Missense
- Variant Prioritization Score for Impact Estimate 0.348
- REVEL 0.18
- CADD 21.50
- PolyPhen-2 0.99
- SIFT 0.08
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available