P77L (p.Pro77Leu) variant of MECOM (Q03112)
P77L (p.Pro77Leu) in MECOM (Q03112) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases.
P77L (p.Pro77Leu) variant details
- p.Pro77Leu
- cosmic curated COSV72110
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance