S56F (p.Ser56Phe) variant of AKT2 (P31751)
S56F (p.Ser56Phe) 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.
S56F (p.Ser56Phe) variant details
- p.Ser56Phe
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10025
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available