S99F (p.Ser99Phe) variant of ATP13A2 (Q9NQ11)
S99F (p.Ser99Phe) 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.
S99F (p.Ser99Phe) variant details
- p.Ser99Phe
- NCI-TCGA Cosmic COSV5869
- cosmic curated COSV58699
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available