S59G (p.Ser59Gly) variant of SLC22A1 (O15245)
S59G (p.Ser59Gly) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
S59G (p.Ser59Gly) variant details
- p.Ser59Gly
- gnomAD 6-160122110-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.28
- CADD 22.40
- PolyPhen-2 0.07
- SIFT 0.04
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available