E98G (p.Glu98Gly) variant of MYH11 (Myosin-11)
E98G (p.Glu98Gly) in MYH11 (Myosin-11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E98G (p.Glu98Gly) variant details
- p.Glu98Gly
- NCI-TCGA Cosmic COSV5556
- cosmic curated COSV55567
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available