S123F (p.Ser123Phe) variant of ATP13A2 (Q9NQ11)
S123F (p.Ser123Phe) in ATP13A2 (Q9NQ11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S123F (p.Ser123Phe) variant details
- p.Ser123Phe
- NCI-TCGA Cosmic COSV5870
- cosmic curated COSV58702
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available