A69G (p.Ala69Gly) variant of HSD17B3 (P37058)
A69G (p.Ala69Gly) in HSD17B3 (P37058) is a missense change. The record also includes variant effect predictions and structural context.
A69G (p.Ala69Gly) variant details
- p.Ala69Gly
- Ensembl rs1825570777
- Missense
- MetaLR 0.84
- MetaSVM 0.85
- SIFT 0.00
- Structural context available