R13G (p.Arg13Gly) variant of SMARCA4 (P51532)
R13G (p.Arg13Gly) in SMARCA4 (P51532) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R13G (p.Arg13Gly) variant details
- p.Arg13Gly
- Ensembl rs1568416700
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available