L13Q (p.Leu13Gln) variant of FGFR1 (P11362)
L13Q (p.Leu13Gln) 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.
L13Q (p.Leu13Gln) variant details
- p.Leu13Gln
- ExAC rs764533580
- TOPMed rs764533580
- gnomAD rs764533580
- Uncertain significance
- Missense
- MetaLR 0.59
- MetaSVM 0.28
- SIFT 0.02
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available