G97R (p.Gly97Arg) variant of HSD17B3 (P37058)
G97R (p.Gly97Arg) in HSD17B3 (P37058) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
G97R (p.Gly97Arg) variant details
- p.Gly97Arg
- Ensembl rs1564030988
- Missense
- Variant Prioritization Score for Impact Estimate 0.555
- REVEL 0.52
- MetaLR 0.81
- MetaSVM 0.32
- CADD 23.80
- PolyPhen-2 1.00
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available