R57D (p.Arg57Asp) variant of SLC12A1 (Q13621)
R57D (p.Arg57Asp) in SLC12A1 (Q13621) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R57D (p.Arg57Asp) variant details
- p.Arg57Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available