F108L (p.Phe108Leu) variant of HSPG2 (P98160)
F108L (p.Phe108Leu) in HSPG2 (P98160) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data.
F108L (p.Phe108Leu) variant details
- p.Phe108Leu
- 1000Genomes rs2501260
- ESP rs2501260
- ExAC rs2501260
- TOPMed rs2501260
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available