C26R (p.Cys26Arg) variant of CSF3R (Q99062)
C26R (p.Cys26Arg) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
C26R (p.Cys26Arg) variant details
- p.Cys26Arg
- ExAC rs776693811
- TOPMed rs776693811
- gnomAD rs776693811
- Missense
- Variant Prioritization Score for Impact Estimate 0.639
- REVEL 0.72
- CADD 24.50
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available