N17N (p.Asn17Asn) variant of AICDA (Q9GZX7)
N17N (p.Asn17Asn) in AICDA (Q9GZX7) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
N17N (p.Asn17Asn) variant details
- p.Asn17Asn
- rs749195364
- gnomAD 12-8606970-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.118
- CADD 5.25
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available