S97N (p.Ser97Asn) variant of SLC37A4 (O43826)
S97N (p.Ser97Asn) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
S97N (p.Ser97Asn) variant details
- p.Ser97Asn
- gnomAD rs1312150484
- Missense
- Variant Prioritization Score for Impact Estimate 0.753
- CADD 23.80
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available