F88L (p.Phe88Leu) variant of AKT2 (P31751)
F88L (p.Phe88Leu) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
F88L (p.Phe88Leu) variant details
- p.Phe88Leu
- gnomAD rs1489834693
- Missense
- Variant Prioritization Score for Impact Estimate 0.356
- CADD 9.93
- Most common in the Non-Finnish European population (allele frequency 7.4e-06)
- Structural context available