N134S (p.Asn134Ser) variant of CSF3R (Q99062)
N134S (p.Asn134Ser) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
N134S (p.Asn134Ser) variant details
- p.Asn134Ser
- TOPMed rs1650947311
- Missense
- Variant Prioritization Score for Impact Estimate 0.289
- REVEL 0.14
- CADD 23.20
- PolyPhen-2 0.03
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available