S19C (p.Ser19Cys) variant of FGFR2 (P21802)
S19C (p.Ser19Cys) in FGFR2 (P21802) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
S19C (p.Ser19Cys) variant details
- p.Ser19Cys
- ExAC rs760903123
- TOPMed rs760903123
- gnomAD rs760903123
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available