G27A (p.Gly27Ala) variant of CSF3R (Q99062)
G27A (p.Gly27Ala) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
G27A (p.Gly27Ala) variant details
- p.Gly27Ala
- gnomAD rs1428477464
- Missense
- Variant Prioritization Score for Impact Estimate 0.458
- REVEL 0.38
- CADD 19.10
- PolyPhen-2 0.77
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available