S47G (p.Ser47Gly) variant of CSF1R (P07333)
S47G (p.Ser47Gly) in CSF1R (P07333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data.
S47G (p.Ser47Gly) variant details
- p.Ser47Gly
- ExAC rs774944970
- gnomAD rs774944970
- Missense
- Variant Prioritization Score for Impact Estimate 0.405
- CADD 17.50
- PolyPhen-2 0.18
- SIFT 0.23
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)