E48D (p.Glu48Asp) variant of ATP1A2 (P50993)
E48D (p.Glu48Asp) in ATP1A2 (P50993) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E48D (p.Glu48Asp) variant details
- p.Glu48Asp
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10076
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available