F116S (p.Phe116Ser) variant of NCF2 (Neutrophil cytosol factor 2)
F116S (p.Phe116Ser) in NCF2 (Neutrophil cytosol factor 2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
F116S (p.Phe116Ser) variant details
- p.Phe116Ser
- TOPMed rs1672854639
- gnomAD rs1672854639
- Missense
- Variant Prioritization Score for Impact Estimate 0.643
- REVEL 0.70
- MetaLR 0.53
- MetaSVM -0.18
- CADD 26.70
- SIFT 0.42
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available