D40G (p.Asp40Gly) variant of BRAF (P15056)
D40G (p.Asp40Gly) in BRAF (P15056) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes experimental measurements and structural context.
D40G (p.Asp40Gly) variant details
- p.Asp40Gly
- Ensembl rs1818656083
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- BRAF Raf-like Ras-binding domain domainome 1.0: score 0.0364