L26P (p.Leu26Pro) variant of BMPR1A (P36894)
L26P (p.Leu26Pro) in BMPR1A (P36894) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
L26P (p.Leu26Pro) variant details
- p.Leu26Pro
- 1000Genomes rs200307579
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available