Q16H (p.Gln16His) variant of BRAF (P15056)
Q16H (p.Gln16His) in BRAF (P15056) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes experimental measurements and structural context.
Q16H (p.Gln16His) variant details
- p.Gln16His
- rs1563042542
- ClinGen CA369590202
- ClinVar RCV000681056
- Ensembl rs1563042542
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.38
- AlphaMissense 0.16
- MetaLR 0.17
- MetaSVM -0.91
- PolyPhen-2 0.22
- SIFT 0.34
- MutPred 0.20
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- BRAF Raf-like Ras-binding domain domainome 1.0: score -0.0217