I7F (p.Ile7Phe) variant of AKT2 (P31751)
I7F (p.Ile7Phe) in AKT2 (P31751) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
I7F (p.Ile7Phe) variant details
- p.Ile7Phe
- 1000Genomes rs199748431
- ExAC rs199748431
- TOPMed rs199748431
- gnomAD rs199748431
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available