T56R (p.Thr56Arg) variant of ARID2 (Q68CP9)
T56R (p.Thr56Arg) in ARID2 (Q68CP9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes variant effect predictions and structural context.
T56R (p.Thr56Arg) variant details
- p.Thr56Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.26
- MetaSVM -0.77
- SIFT 0.00
- UniProt: Variant assessed as somatic; high impact.
- Structural context available