S32T (p.Ser32Thr) variant of ARID2 (Q68CP9)
S32T (p.Ser32Thr) in ARID2 (Q68CP9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S32T (p.Ser32Thr) variant details
- p.Ser32Thr
- NCI-TCGA Cosmic COSV5760
- Ensembl rs868411783
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available