A26G (p.Ala26Gly) variant of SMARCA4 (P51532)
A26G (p.Ala26Gly) in SMARCA4 (P51532) 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 structural context.
A26G (p.Ala26Gly) variant details
- p.Ala26Gly
- Ensembl rs1599928845
- 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