G18E (p.Gly18Glu) variant of SMARCA2 (P51531)
G18E (p.Gly18Glu) in SMARCA2 (P51531) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign in the context of not provided. The record also includes structural context.
G18E (p.Gly18Glu) variant details
- p.Gly18Glu
- rs2537192540
- ClinGen CA372779062
- ClinVar RCV003580630
- Benign
- not provided
- Missense
- ClinVar: Benign (not provided)
- EBI: Benign
- UniProt: Benign
- Structural context available