R53S (p.Arg53Ser) variant of ARID2 (Q68CP9)
R53S (p.Arg53Ser) in ARID2 (Q68CP9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R53S (p.Arg53Ser) variant details
- p.Arg53Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available