R38R (p.Arg38Arg) variant of NOD2 (Q9HC29)
R38R (p.Arg38Arg) in NOD2 (Q9HC29) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
R38R (p.Arg38Arg) variant details
- p.Arg38Arg
- gnomAD 16-50699672-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.291
- CADD 9.92
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available