T108A (p.Thr108Ala) variant of SMARCE1 (Q969G3)
T108A (p.Thr108Ala) in SMARCE1 (Q969G3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes published literature and structural context.
T108A (p.Thr108Ala) variant details
- p.Thr108Ala
- rs2508604586
- ClinGen CA399367181
- ClinVar RCV004508450
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)