W34R (p.Trp34Arg) variant of FGFR1 (P11362)
W34R (p.Trp34Arg) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
W34R (p.Trp34Arg) variant details
- p.Trp34Arg
- Ensembl rs2150967212
- Missense
- Variant Prioritization Score for Impact Estimate 0.394
- REVEL 0.35
- CADD 22.60
- PolyPhen-2 0.01
- SIFT 0.56
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available