F38F (p.Phe38Phe) variant of FTO (Q9C0B1)
F38F (p.Phe38Phe) in FTO (Q9C0B1) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- rs780803760
- gnomAD 16-53810208-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.333
- CADD 9.96
- Most common in the South Asian population (allele frequency 4.7e-05)
- Structural context available
- Literature evidence available