S66N (p.Ser66Asn) variant of CSF1R (P07333)
S66N (p.Ser66Asn) in CSF1R (P07333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data.
S66N (p.Ser66Asn) variant details
- p.Ser66Asn
- cosmic curated COSV53843
- TOPMed rs1758508093
- Missense
- Variant Prioritization Score for Impact Estimate 0.171
- CADD 4.94
- PolyPhen-2 0.08
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)