M56V (p.Met56Val) variant of SOST (Sclerostin)
M56V (p.Met56Val) in SOST (Sclerostin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
M56V (p.Met56Val) variant details
- p.Met56Val
- NCI-TCGA Cosmic COSV5701
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available