G33E (p.Gly33Glu) variant of SMARCB1 (Q12824)
G33E (p.Gly33Glu) in SMARCB1 (Q12824) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes experimental measurements and structural context.
G33E (p.Gly33Glu) variant details
- p.Gly33Glu
- NCI-TCGA Cosmic COSV5409
- Ensembl rs2145959876
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available
- SMARCB1 SNF5/SMARCB1/INI1 domain domainome 1.0: score -0.421