G7D (p.Gly7Asp) variant of BRAF (P15056)
G7D (p.Gly7Asp) in BRAF (P15056) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes experimental measurements and structural context.
G7D (p.Gly7Asp) variant details
- p.Gly7Asp
- rs2536968672
- ClinGen CA369590258
- ClinVar RCV002281790
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- BRAF Raf-like Ras-binding domain domainome 1.0: score -0.458