V18V (p.Val18Val) variant of NOD2 (Q9HC29)
V18V (p.Val18Val) in NOD2 (Q9HC29) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
V18V (p.Val18Val) variant details
- p.Val18Val
- gnomAD 16-50697297-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.412
- CADD 0.70
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available