R22W (p.Arg22Trp) variant of FGFR1 (P11362)
R22W (p.Arg22Trp) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes variant effect predictions and structural context.
R22W (p.Arg22Trp) variant details
- p.Arg22Trp
- ESP rs148343099
- ExAC rs148343099
- TOPMed rs148343099
- gnomAD rs148343099
- Uncertain significance
- Missense
- MetaLR 0.53
- MetaSVM 0.05
- SIFT 0.01
- EBI: Variant of uncertain significance (in dbSNP:rs17175750)
- UniProt: Uncertain significance (in dbSNP:rs17175750)
- Structural context available