F9I (p.Phe9Ile) variant of FGFR1 (P11362)
F9I (p.Phe9Ile) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
F9I (p.Phe9Ile) variant details
- p.Phe9Ile
- ExAC rs750602076
- TOPMed rs750602076
- gnomAD rs750602076
- Missense
- Variant Prioritization Score for Impact Estimate 0.36
- REVEL 0.28
- CADD 16.90
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available