S28G (p.Ser28Gly) variant of CHRNA4 (P43681)
S28G (p.Ser28Gly) in CHRNA4 (P43681) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data.
S28G (p.Ser28Gly) variant details
- p.Ser28Gly
- ExAC rs768015799
- gnomAD rs768015799
- Missense
- Variant Prioritization Score for Impact Estimate 0.0674
- REVEL 0.03
- CADD 7.59
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the South Asian population (allele frequency 2.3e-05)