F29C (p.Phe29Cys) variant of MYL2 (P10916)
F29C (p.Phe29Cys) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F29C (p.Phe29Cys) variant details
- p.Phe29Cys
- NCI-TCGA Cosmic COSV5740
- cosmic curated COSV57406
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available