I92= variant of HSD17B3 (P37058)
I92= in HSD17B3 (P37058) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes population frequency data and structural context.
I92= variant details
- rs143401138
- NCI-TCGA Cosmic COSV6455
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Population evidence available
- Structural context available