N56N (p.Asn56Asn) variant of SLC18A2 (Q05940)
N56N (p.Asn56Asn) in SLC18A2 (Q05940) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
N56N (p.Asn56Asn) variant details
- p.Asn56Asn
- rs763031075
- gnomAD 10-117244017-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.092
- CADD 1.60
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available