R69H (p.Arg69His) variant of NOD1 (Q9Y239)
R69H (p.Arg69His) in NOD1 (Q9Y239) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
R69H (p.Arg69His) variant details
- p.Arg69His
- rs768166122
- ClinGen CA4205281
- ClinVar RCV004197064
- ExAC rs768166122
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.718
- REVEL 0.65
- CADD 28.00
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available