F38F (p.Phe38Phe) variant of IFNG (Interferon gamma)
F38F (p.Phe38Phe) in IFNG (Interferon gamma) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- rs1420760098
- gnomAD 12-68159502-A-G
- Splice Region
- Variant Prioritization Score for Impact Estimate 0.259
- CADD 16.00
- Most common in the South Asian population (allele frequency 4.9e-05)
- Structural context available
- Literature evidence available