S26N (p.Ser26Asn) variant of CSF1R (P07333)
S26N (p.Ser26Asn) in CSF1R (P07333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data.
S26N (p.Ser26Asn) variant details
- p.Ser26Asn
- gnomAD rs1188913271
- Missense
- Variant Prioritization Score for Impact Estimate 0.251
- CADD 9.14
- PolyPhen-2 0.00
- SIFT 0.50
- Most common in the East Asian population (allele frequency 5e-05)