P57R (p.Pro57Arg) variant of CSF3R (Q99062)
P57R (p.Pro57Arg) in CSF3R (Q99062) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P57R (p.Pro57Arg) variant details
- p.Pro57Arg
- ExAC rs746657668
- TOPMed rs746657668
- gnomAD rs746657668
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available