L12F (p.Leu12Phe) variant of ATP6V1B1 (P15313)
L12F (p.Leu12Phe) 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.
L12F (p.Leu12Phe) variant details
- p.Leu12Phe
- NCI-TCGA Cosmic COSV5226
- NCI-TCGA Cosmic COSV9931
- cosmic curated COSV99313
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available