Y39C (p.Tyr39Cys) variant of ABCC2 (Q92887)
Y39C (p.Tyr39Cys) in ABCC2 (Q92887) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
Y39C (p.Tyr39Cys) variant details
- p.Tyr39Cys
- 1000Genomes rs927344
- ESP rs927344
- ExAC rs927344
- TOPMed rs927344
- Benign
- Missense
- EBI: Benign (in dbSNP:rs927344)
- UniProt: Benign (in dbSNP:rs927344)
- Population evidence available
- Structural context available