A56P (p.Ala56Pro) variant of CHRNA4 (P43681)
A56P (p.Ala56Pro) in CHRNA4 (P43681) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data.
A56P (p.Ala56Pro) variant details
- p.Ala56Pro
- ExAC rs763826732
- gnomAD rs763826732
- Missense
- Variant Prioritization Score for Impact Estimate 0.318
- REVEL 0.03
- CADD 21.90
- PolyPhen-2 0.04
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)