S87F (p.Ser87Phe) variant of ATP6V1A (P38606)
S87F (p.Ser87Phe) in ATP6V1A (P38606) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S87F (p.Ser87Phe) variant details
- p.Ser87Phe
- NCI-TCGA Cosmic COSV5636
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available