V52A (p.Val52Ala) variant of ATP6V1B1 (P15313)
V52A (p.Val52Ala) 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.
V52A (p.Val52Ala) variant details
- p.Val52Ala
- NCI-TCGA Cosmic COSV5227
- cosmic curated COSV52272
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available