P9H (p.Pro9His) variant of ATP6V1B1 (P15313)
P9H (p.Pro9His) in ATP6V1B1 (P15313) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P9H (p.Pro9His) variant details
- p.Pro9His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available