E91D (p.Glu91Asp) variant of HTT (Huntingtin)
E91D (p.Glu91Asp) in HTT (Huntingtin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes variant effect predictions and structural context.
E91D (p.Glu91Asp) variant details
- p.Glu91Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- MetaLR 0.09
- MetaSVM -1.07
- SIFT 0.22
- UniProt: Variant assessed as somatic; high impact.
- Structural context available