A2V (p.Ala2Val) variant of ATP6V1B1 (P15313)
A2V (p.Ala2Val) 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.
A2V (p.Ala2Val) variant details
- p.Ala2Val
- NCI-TCGA Cosmic COSV5226
- cosmic curated COSV52266
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available