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BRAF c.1799_1803delinsAT ;(p.V600_K601delinsD)
Variant ID: 7-140453132-TTTCA-AT
NM_004333.4(
BRAF
):c.1799_1803delinsAT;(p.V600_K601delinsD)
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:
DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research.
Frontiers In Genetics
Cui, Yunlong Y; Li, Hongfeng H; Liu, Pengfei P; Wang, Hailong H; Zhang, Zhenzhen Z; Qu, Hongzhu H; Tian, Caijuan C; Fang, Xiangdong X
Publication Date: 2022
Variant appearance in text: BRAF: 1799_1803delinsAT
PubMed Link:
36685970
Variant Present in the following documents:
Table4.xlsx, sheet 1
View BVdb publication page
The clinical response to vemurafenib in a patient with a rare BRAFV600DK601del mutation-positive melanoma.
Bmc Cancer
Trudel, Stéphanie S; Odolczyk, Norbert N; Dremaux, Julie J; Toffin, Jérôme J; Regnier, Aline A; Sevestre, Henri H; Zielenkiewicz, Piotr P; Arnault, Jean-Philippe JP; Gubler, Brigitte B
Publication Date: 2014-09-29
Variant appearance in text: BRAF: 1799_1803delinsAT
PubMed Link:
25265970
Variant Present in the following documents:
Main text
12885_2014_Article_4910.pdf
View BVdb publication page