V8G (p.Val8Gly) variant of HNF4A (P41235)
V8G (p.Val8Gly) in HNF4A (P41235) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V8G (p.Val8Gly) variant details
- p.Val8Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available