N69S (p.Asn69Ser) variant of MYLK (Q15746)
N69S (p.Asn69Ser) 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.
N69S (p.Asn69Ser) variant details
- p.Asn69Ser
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10065
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available