Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRAF c.1766C>A ;(p.T589K)
Variant ID: 7-140453169-G-T
NM_004333.4(
BRAF
):c.1766C>A;(p.T589K)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Significant Improvement in Detecting BRAF, KRAS, and EGFR Mutations Using Next-Generation Sequencing as Compared with FDA-Cleared Kits.
Molecular Diagnosis & Therapy
Ma, Wanlong W; Brodie, Steven S; Agersborg, Sally S; Funari, Vincent A VA; Albitar, Maher M
Publication Date: 2017-10
Variant appearance in text: BRAF: 1766C>A; Thr589Lys
PubMed Link:
28639239
Variant Present in the following documents:
Main text
40291_2017_Article_290.pdf
View BVdb publication page