A28V (p.Ala28Val) variant of PIK3CG (P48736)
A28V (p.Ala28Val) in PIK3CG (P48736) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A28V (p.Ala28Val) variant details
- p.Ala28Val
- NCI-TCGA TCGA novel
- gnomAD rs1341469233
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available