L78M (p.Leu78Met) variant of AKT2 (P31751)
L78M (p.Leu78Met) in AKT2 (P31751) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L78M (p.Leu78Met) variant details
- p.Leu78Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available