G37R (p.Gly37Arg) variant of AKT2 (P31751)
G37R (p.Gly37Arg) 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.
G37R (p.Gly37Arg) variant details
- p.Gly37Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available