F39F (p.Phe39Phe) variant of NCF4 (Neutrophil cytosol factor 4)
F39F (p.Phe39Phe) in NCF4 (Neutrophil cytosol factor 4) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
F39F (p.Phe39Phe) variant details
- p.Phe39Phe
- gnomAD 22-36864129-T-C
- Splice Region
- Variant Prioritization Score for Impact Estimate 0.159
- CADD 11.10
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available
- Literature evidence available