N86D (p.Asn86Asp) variant of CHRNA4 (P43681)
N86D (p.Asn86Asp) in CHRNA4 (P43681) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data.
N86D (p.Asn86Asp) variant details
- p.Asn86Asp
- Ensembl rs1021423232
- Missense
- Variant Prioritization Score for Impact Estimate 0.765
- REVEL 0.86
- CADD 27.40
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)