N8N (p.Asn8Asn) variant of SLC6A19 (Q695T7)
N8N (p.Asn8Asn) in SLC6A19 (Q695T7) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
N8N (p.Asn8Asn) variant details
- p.Asn8Asn
- rs557180261
- gnomAD 5-1201674-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.186
- CADD 4.39
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available