G5S (p.Gly5Ser) variant of NOD2 (Q9HC29)
G5S (p.Gly5Ser) in NOD2 (Q9HC29) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
G5S (p.Gly5Ser) variant details
- p.Gly5Ser
- gnomAD 16-50697256-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.169
- MetaLR 0.13
- MetaSVM -0.99
- CADD 9.81
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available
- Literature evidence available