G39R (p.Gly39Arg) variant of CSF3R (Q99062)
G39R (p.Gly39Arg) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data and structural context.
G39R (p.Gly39Arg) variant details
- p.Gly39Arg
- gnomAD rs1651090445
- Missense
- Variant Prioritization Score for Impact Estimate 0.696
- REVEL 0.71
- CADD 25.60
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available