W36* (p.Trp36Ter) variant of HSD17B3 (P37058)
W36* (p.Trp36Ter) in HSD17B3 (P37058) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
W36* (p.Trp36Ter) variant details
- p.Trp36Ter
- NCI-TCGA Cosmic COSV6455
- cosmic curated COSV64557
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.
- Structural context available