G35R (p.Gly35Arg) variant of FGFR1 (P11362)
G35R (p.Gly35Arg) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
G35R (p.Gly35Arg) variant details
- p.Gly35Arg
- ExAC rs773442656
- TOPMed rs773442656
- gnomAD rs773442656
- Missense
- Variant Prioritization Score for Impact Estimate 0.469
- REVEL 0.28
- CADD 22.60
- PolyPhen-2 0.00
- SIFT 0.51
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available