BRAF Codon 257 Missense
Associated Genetic Biomarkers
BRAF Codon 257 Missense is present in 0.01% of AACR GENIE cases, with duodenal adenocarcinoma, endometrial endometrioid adenocarcinoma, large cell neuroendocrine carcinoma, and small intestinal carcinoma having the greatest prevalence .
BRAF Codon 257 Missense serves as an inclusion eligibility criterion in 1 clinical trial, of which 1 is open and 0 are closed. Of the trial that contains BRAF Codon 257 Missense as an inclusion criterion, 1 is phase 2 (1 open).
Trials with BRAF Codon 257 Missense in the inclusion eligibility criteria most commonly target malignant solid tumor and melanoma .
Binimetinib and encorafenib are the most frequent therapies in trials with BRAF Codon 257 Missense as an inclusion criteria .
Significance of BRAF Codon 257 Missense in Diseases
Malignant Solid Tumor +
BRAF is altered in 6.59% of malignant solid tumor patients with BRAF Codon 257 Missense present in 0.0% of all malignant solid tumor patients .
BRAF Codon 257 Missense is an inclusion criterion in 1 clinical trial for malignant solid tumor, of which 1 is open and 0 are closed. Of the trial that contains BRAF Codon 257 Missense and malignant solid tumor as inclusion criteria, 1 is phase 2 (1 open) .
2. The UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Research. 2019;47:D506-D515.
3. Liu X, Wu C, Li C, and Boerwinkle E. dbNSFP v3.0: A one-stop database of functional predictions and annotations for human nonsynonymous and splice site SNVs. Human Mutation. 2015;37:235-241.
Liu X, Jian X, and Boerwinkle E. dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 2011;32:894-899.
4. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.