F38F (p.Phe38Phe) variant of TNF (Tumor necrosis factor)
F38F (p.Phe38Phe) in TNF (Tumor necrosis factor) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- gnomAD 6-31575855-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.38
- CADD 12.20
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available