W99C (p.Trp99Cys) variant of AKT2 (P31751)
W99C (p.Trp99Cys) in AKT2 (P31751) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
W99C (p.Trp99Cys) variant details
- p.Trp99Cys
- rs879685586
- gnomAD 19-40234510-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.241
- CADD 6.56
- Population evidence available
- Structural context available
- Literature evidence available