Q79H (p.Gln79His) variant of MYH6 (Myosin-6)
Q79H (p.Gln79His) 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.
Q79H (p.Gln79His) variant details
- p.Gln79His
- NCI-TCGA Cosmic COSV6245
- cosmic curated COSV62450
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available