L49M (p.Leu49Met) variant of MYL2 (P10916)
L49M (p.Leu49Met) 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.
L49M (p.Leu49Met) variant details
- p.Leu49Met
- NCI-TCGA Cosmic COSV9996
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available