P68S (p.Pro68Ser) variant of AKT2 (P31751)
P68S (p.Pro68Ser) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
P68S (p.Pro68Ser) variant details
- p.Pro68Ser
- Ensembl rs2145293995
- Missense
- Variant Prioritization Score for Impact Estimate 0.469
- REVEL 0.31
- AlphaMissense 0.99
- MetaLR 0.24
- MetaSVM -0.66
- CADD 24.50
- PolyPhen-2 0.70
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available