E106D (p.Glu106Asp) variant of MTHFR (P42898)
E106D (p.Glu106Asp) in MTHFR (P42898) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E106D (p.Glu106Asp) variant details
- p.Glu106Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available