S13Y (p.Ser13Tyr) variant of MYPN (Myopalladin)
S13Y (p.Ser13Tyr) in MYPN (Myopalladin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S13Y (p.Ser13Tyr) variant details
- p.Ser13Tyr
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10058
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available