F36Y (p.Phe36Tyr) variant of AIP (AH receptor-interacting protein)
F36Y (p.Phe36Tyr) in AIP (AH receptor-interacting protein) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
F36Y (p.Phe36Tyr) variant details
- p.Phe36Tyr
- ExAC rs765126288
- gnomAD rs765126288
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available