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BRAF c.1860+712G>C
Variant ID: 7-140452363-C-G
NM_004333.4(
BRAF
):c.1860+712G>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Combined Mutational and Clonality Analyses Support the Existence of Intra-Tumor Heterogeneity in Papillary Thyroid Cancer.
Journal Of Clinical Medicine
Muzza, Marina M; Pogliaghi, Gabriele G; Persani, Luca L; Fugazzola, Laura L; Colombo, Carla C
Publication Date: 2021-06-16
Variant appearance in text: rs10232557
PubMed Link:
34208446
Variant Present in the following documents:
Main text
jcm-10-02645.pdf
View BVdb publication page
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs10232557
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page