I127T (p.Ile127Thr) variant of HSD17B3 (P37058)
I127T (p.Ile127Thr) 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.
I127T (p.Ile127Thr) variant details
- p.Ile127Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.66
- MetaSVM 0.45
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available