I77M (p.Ile77Met) variant of BRAF (P15056)
I77M (p.Ile77Met) in BRAF (P15056) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of RASopathy. The record also includes structural context.
I77M (p.Ile77Met) variant details
- p.Ile77Met
- rs2536569627
- ClinGen CA369587704
- ClinVar RCV002820949
- Uncertain significance
- RASopathy
- Missense
- ClinVar: Uncertain significance (RASopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available