G49V (p.Gly49Val) variant of MYPN (Myopalladin)
G49V (p.Gly49Val) 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.
G49V (p.Gly49Val) variant details
- p.Gly49Val
- NCI-TCGA Cosmic COSV6273
- cosmic curated COSV62731
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available