A67T (p.Ala67Thr) variant of CSF3R (Q99062)
A67T (p.Ala67Thr) in CSF3R (Q99062) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A67T (p.Ala67Thr) variant details
- p.Ala67Thr
- ExAC rs756473038
- gnomAD rs756473038
- Missense
- Variant Prioritization Score for Impact Estimate 0.173
- REVEL 0.25
- CADD 0.10
- PolyPhen-2 0.00
- SIFT 0.71
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available