H13Q (p.His13Gln) variant of AKT1 (P31749)
H13Q (p.His13Gln) in AKT1 (P31749) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H13Q (p.His13Gln) variant details
- p.His13Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available