S52T (p.Ser52Thr) variant of SMARCA2 (P51531)
S52T (p.Ser52Thr) in SMARCA2 (P51531) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
S52T (p.Ser52Thr) variant details
- p.Ser52Thr
- rs2537192938
- ClinGen CA372779268
- ClinVar RCV003556628
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available