P45A (p.Pro45Ala) variant of AKT2 (P31751)
P45A (p.Pro45Ala) in AKT2 (P31751) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
P45A (p.Pro45Ala) variant details
- p.Pro45Ala
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10025
- NCI-TCGA Cosmic COSV6090
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available