S59N (p.Ser59Asn) variant of SLC22A1 (O15245)
S59N (p.Ser59Asn) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
S59N (p.Ser59Asn) variant details
- p.Ser59Asn
- TOPMed rs1028655210
- Missense
- Variant Prioritization Score for Impact Estimate 0.447
- REVEL 0.35
- CADD 24.50
- PolyPhen-2 0.87
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available