E61D (p.Glu61Asp) variant of MYLK (Q15746)
E61D (p.Glu61Asp) in MYLK (Q15746) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E61D (p.Glu61Asp) variant details
- p.Glu61Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available