V57L (p.Val57Leu) variant of AKT2 (P31751)
V57L (p.Val57Leu) in AKT2 (P31751) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V57L (p.Val57Leu) variant details
- p.Val57Leu
- TOPMed rs1407888862
- gnomAD rs1407888862
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10025
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available