Q76K (p.Gln76Lys) variant of CSF3R (Q99062)
Q76K (p.Gln76Lys) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
Q76K (p.Gln76Lys) variant details
- p.Gln76Lys
- TOPMed rs1188234060
- gnomAD rs1188234060
- Missense
- Variant Prioritization Score for Impact Estimate 0.236
- REVEL 0.17
- CADD 10.10
- PolyPhen-2 0.04
- SIFT 0.37
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available