Varaico: Literature-Extracted Genetic Variants

Gene:BRAF
Variant:p.A39T
Back to variants list

BRAF

NM_004333.6:p.A39T

Associated Papers

Oncogenic composite mutations can be predicted by co-mutations and their chromosomal location.

Küçükosmanoglu A et al.

Molecular Oncology, 2024

38757376 (PubMed )
Supplement: MOL2-18-2407-s001.xlsx › 1E_Excluded_datasets

BRAFV600E/pTERT double mutated papillary thyroid cancers exhibit immune gene suppression.

Sigarteu Chindris AM et al.

Frontiers in Endocrinology, 2024

39717106 (PubMed )
Supplement: Table8.xlsx › S_Tab._8_TCGA

Source, co-occurrence, and prognostic value of PTEN mutations or loss in colorectal cancer.

Serebriiskii IG et al.

Npj Genomic Medicine, 2023

38001126 (PubMed )
Supplement: 41525_2023_384_MOESM1_ESM.xlsx › Table_S6

Recapitulating thyroid cancer histotypes through engineering embryonic stem cells.

Veschi V et al.

Nature Communications, 2023

36906579 (PubMed )
Supplement: 41467_2023_36922_MOESM6_ESM.zip › 356656_2_data_0_rq37ls.xlsx › Figure_2f

Spectrum of BRAF Aberrations and Its Potential Clinical Implications: Insights From Integrative Pan-Cancer Analysis.

Yi Q et al.

Frontiers in Bioengineering and Biotechnology, 2022

35910024 (PubMed )
Supplement: Table2.XLSX › table

Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.

Hescheler DA et al.

Frontiers in Endocrinology, 2021

34630336 (PubMed )
Supplement: Table_1.xlsx › Tab3
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."