L69F (p.Leu69Phe) variant of CSF3R (Q99062)
L69F (p.Leu69Phe) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
L69F (p.Leu69Phe) variant details
- p.Leu69Phe
- TOPMed rs1415537596
- gnomAD rs1415537596
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.13
- CADD 4.11
- PolyPhen-2 0.01
- SIFT 0.61
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available