S35W (p.Ser35Trp) variant of SMARCA4 (P51532)
S35W (p.Ser35Trp) in SMARCA4 (P51532) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
S35W (p.Ser35Trp) variant details
- p.Ser35Trp
- 1000Genomes rs563079629
- ExAC rs563079629
- TOPMed rs563079629
- gnomAD rs563079629
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available