M89I (p.Met89Ile) variant of LEP (Leptin)
M89I (p.Met89Ile) in LEP (Leptin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
M89I (p.Met89Ile) variant details
- p.Met89Ile
- NCI-TCGA Cosmic COSV1004
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available