G19S (p.Gly19Ser) variant of SMARCA4 (P51532)
G19S (p.Gly19Ser) in SMARCA4 (P51532) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G19S (p.Gly19Ser) variant details
- p.Gly19Ser
- cosmic curated COSV10465
- Ensembl rs2145721640
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available