N38N (p.Asn38Asn) variant of GABRA1 (P14867)
N38N (p.Asn38Asn) in GABRA1 (P14867) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
N38N (p.Asn38Asn) variant details
- p.Asn38Asn
- rs890318955
- gnomAD 5-161850664-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.6
- CADD 21.70
- Most common in the Ashkenazi Jewish population (allele frequency 5.3e-05)
- Structural context available
- Literature evidence available