A89V (p.Ala89Val) variant of HSD17B3 (P37058)
A89V (p.Ala89Val) in HSD17B3 (P37058) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
A89V (p.Ala89Val) variant details
- p.Ala89Val
- NCI-TCGA Cosmic COSV6455
- cosmic curated COSV64557
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.81
- MetaSVM 0.30
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available