S42R (p.Ser42Arg) variant of IL6R (P08887)
S42R (p.Ser42Arg) in IL6R (P08887) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
S42R (p.Ser42Arg) variant details
- p.Ser42Arg
- 1000Genomes rs34099703
- ESP rs34099703
- ExAC rs34099703
- TOPMed rs34099703
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available