S31R (p.Ser31Arg) variant of SMARCA4 (P51532)
S31R (p.Ser31Arg) in SMARCA4 (P51532) 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 structural context.
S31R (p.Ser31Arg) variant details
- p.Ser31Arg
- Ensembl rs2145722956
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available