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.




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