S19T (p.Ser19Thr) variant of MYH6 (Myosin-6)
S19T (p.Ser19Thr) in MYH6 (Myosin-6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S19T (p.Ser19Thr) variant details
- p.Ser19Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available