A91T (p.Ala91Thr) variant of MYH6 (Myosin-6)
A91T (p.Ala91Thr) 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.
A91T (p.Ala91Thr) variant details
- p.Ala91Thr
- NCI-TCGA Cosmic COSV6244
- cosmic curated COSV62448
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available