N27N (p.Asn27Asn) variant of SLC12A1 (Q13621)
N27N (p.Asn27Asn) in SLC12A1 (Q13621) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
N27N (p.Asn27Asn) variant details
- p.Asn27Asn
- rs746746098
- gnomAD 15-48207800-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.103
- CADD 3.15
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available