I12N (p.Ile12Asn) variant of NOD1 (Q9Y239)
I12N (p.Ile12Asn) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
I12N (p.Ile12Asn) variant details
- p.Ile12Asn
- TOPMed rs1562698027
- Missense
- Variant Prioritization Score for Impact Estimate 0.157
- REVEL 0.20
- CADD 4.71
- PolyPhen-2 0.04
- SIFT 0.27
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available