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BRAF c.1831G>C ;(p.E611Q)
Variant ID: 7-140453104-C-G
NM_004333.4(
BRAF
):c.1831G>C;(p.E611Q)
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:
Characteristics of and Treatment Strategies for Advanced EGFR-Mutant NSCLC With Concomitant BRAF Variations.
Jto Clinical And Research Reports
Wei, Xue-Wu XW; Deng, Jia-Yi JY; Xu, Chong-Rui CR; Chen, Zhi-Hong ZH; Zhu, Dong-Qin DQ; Wu, Qian Q; Zhang, Xu-Chao XC; Wu, Yi-Long YL; Zhou, Qing Q
Publication Date: 2022-07
Variant appearance in text: BRAF: E611Q
PubMed Link:
35789792
Variant Present in the following documents:
Main text
mmc3.xlsx, sheet 4
mmc3.xlsx, sheet 1
main.pdf
View BVdb publication page
Clinical detection and categorization of uncommon and concomitant mutations involving BRAF.
Bmc Cancer
Zheng, Gang G; Tseng, Li-Hui LH; Chen, Guoli G; Haley, Lisa L; Illei, Peter P; Gocke, Christopher D CD; Eshleman, James R JR; Lin, Ming-Tseh MT
Publication Date: 2015-10-24
Variant appearance in text: BRAF: 1831G>C; E611Q
PubMed Link:
26498038
Variant Present in the following documents:
Main text
View BVdb publication page