F22F (p.Phe22Phe) variant of TG (Thyroglobulin)
F22F (p.Phe22Phe) in TG (Thyroglobulin) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
F22F (p.Phe22Phe) variant details
- p.Phe22Phe
- rs143647619
- gnomAD 8-132867066-C-T
- Splice Region
- Variant Prioritization Score for Impact Estimate 0.0984
- CADD 2.50
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available