G10W (p.Gly10Trp) variant of MYH7 (Myosin-7)
G10W (p.Gly10Trp) in MYH7 (Myosin-7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G10W (p.Gly10Trp) variant details
- p.Gly10Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available