E149K (p.Glu149Lys) variant of HSD17B3 (P37058)
E149K (p.Glu149Lys) in HSD17B3 (P37058) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E149K (p.Glu149Lys) variant details
- p.Glu149Lys
- NCI-TCGA Cosmic COSV6455
- cosmic curated COSV64556
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available