R41G (p.Arg41Gly) variant of CSF1R (P07333)
R41G (p.Arg41Gly) in CSF1R (P07333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data.
R41G (p.Arg41Gly) variant details
- p.Arg41Gly
- TOPMed rs1391926262
- gnomAD rs1391926262
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- CADD 21.90
- PolyPhen-2 0.95
- SIFT 0.03
- Population evidence available