S22N (p.Ser22Asn) variant of SLC37A4 (O43826)
S22N (p.Ser22Asn) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data and structural context.
S22N (p.Ser22Asn) variant details
- p.Ser22Asn
- gnomAD rs1194300027
- Missense
- Variant Prioritization Score for Impact Estimate 0.739
- CADD 23.30
- PolyPhen-2 0.23
- SIFT 0.04
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available