P69H (p.Pro69His) variant of ABCC8 (Q09428)
P69H (p.Pro69His) in ABCC8 (Q09428) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P69H (p.Pro69His) variant details
- p.Pro69His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available