P28H (p.Pro28His) variant of FGFR1 (P11362)
P28H (p.Pro28His) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes structural context.
P28H (p.Pro28His) variant details
- p.Pro28His
- ESP rs145434725
- ExAC rs145434725
- TOPMed rs145434725
- gnomAD rs145434725
- Pathogenic
- Missense
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available