F53I (p.Phe53Ile) variant of MYL2 (P10916)
F53I (p.Phe53Ile) 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.
F53I (p.Phe53Ile) variant details
- p.Phe53Ile
- NCI-TCGA Cosmic COSV9996
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available