F88I (p.Phe88Ile) variant of AKT2 (P31751)
F88I (p.Phe88Ile) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
F88I (p.Phe88Ile) variant details
- p.Phe88Ile
- gnomAD 19-40234560-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.422
- CADD 2.72
- SIFT 0.03
- Most common in the South Asian population (allele frequency 0.0001)
- Structural context available
- Literature evidence available