L11I (p.Leu11Ile) variant of HSD17B3 (P37058)
L11I (p.Leu11Ile) 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.
L11I (p.Leu11Ile) variant details
- p.Leu11Ile
- NCI-TCGA Cosmic COSV6455
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available