C19W (p.Cys19Trp) variant of FGFR1 (P11362)
C19W (p.Cys19Trp) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
C19W (p.Cys19Trp) variant details
- p.Cys19Trp
- Ensembl rs2151343740
- Missense
- Variant Prioritization Score for Impact Estimate 0.431
- REVEL 0.52
- CADD 23.80
- PolyPhen-2 0.27
- SIFT 0.01
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available