N29N (p.Asn29Asn) variant of SLC12A1 (Q13621)
N29N (p.Asn29Asn) in SLC12A1 (Q13621) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
N29N (p.Asn29Asn) variant details
- p.Asn29Asn
- gnomAD 15-48207806-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.242
- CADD 3.98
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available