N37N (p.Asn37Asn) variant of SLC6A19 (Q695T7)
N37N (p.Asn37Asn) in SLC6A19 (Q695T7) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
N37N (p.Asn37Asn) variant details
- p.Asn37Asn
- gnomAD 5-1201761-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.292
- CADD 9.61
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available