E97D (p.Glu97Asp) variant of SFTPB (P07988)
E97D (p.Glu97Asp) in SFTPB (P07988) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
E97D (p.Glu97Asp) variant details
- p.Glu97Asp
- 1000Genomes rs34682912
- ESP rs34682912
- ExAC rs34682912
- TOPMed rs34682912
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available