G138S (p.Gly138Ser) variant of NOD1 (Q9Y239)
G138S (p.Gly138Ser) in NOD1 (Q9Y239) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
G138S (p.Gly138Ser) variant details
- p.Gly138Ser
- TOPMed rs1371276285
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- REVEL 0.18
- CADD 22.10
- PolyPhen-2 0.51
- SIFT 0.68
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available