S152G (p.Ser152Gly) variant of HSD17B3 (P37058)
S152G (p.Ser152Gly) in HSD17B3 (P37058) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
S152G (p.Ser152Gly) variant details
- p.Ser152Gly
- gnomAD rs1359243413
- Missense
- Variant Prioritization Score for Impact Estimate 0.228
- REVEL 0.11
- MetaLR 0.39
- MetaSVM -0.68
- CADD 20.50
- SIFT 0.28
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available