F52I (p.Phe52Ile) variant of MYLK (Q15746)
F52I (p.Phe52Ile) in MYLK (Q15746) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F52I (p.Phe52Ile) variant details
- p.Phe52Ile
- NCI-TCGA Cosmic COSV6060
- cosmic curated COSV60608
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available