R101G (p.Arg101Gly) variant of AKT2 (P31751)
R101G (p.Arg101Gly) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
R101G (p.Arg101Gly) variant details
- p.Arg101Gly
- ExAC rs761956794
- TOPMed rs761956794
- gnomAD rs761956794
- Missense
- Variant Prioritization Score for Impact Estimate 0.35
- REVEL 0.23
- CADD 23.40
- PolyPhen-2 0.07
- SIFT 0.19
- Most common in the Finnish in Finland (FIN) population (allele frequency 2e-05)
- Structural context available