E97G (p.Glu97Gly) variant of AKT2 (P31751)
E97G (p.Glu97Gly) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
E97G (p.Glu97Gly) variant details
- p.Glu97Gly
- gnomAD rs1434565896
- Missense
- Variant Prioritization Score for Impact Estimate 0.733
- REVEL 0.72
- CADD 40.00
- PolyPhen-2 0.77
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available