BRAF c.1799_1800del ;(p.V600Efs*11)

Variant ID: 7-140453134-TCA-T


This variant was identified in 3 publications

View GRCh38 version.


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_1800del
PubMed Link: 36685970
Variant Present in the following documents:
  • Table5.xlsx, sheet 1
View BVdb publication page

Multi-site clonality analysis uncovers pervasive heterogeneity across melanoma metastases.

Nature Communications
Rabbie, Roy R; Ansari-Pour, Naser N; Cast, Oliver O; Lau, Doreen D; Scott, Francis F; Welsh, Sarah J SJ; Parkinson, Christine C; Khoja, Leila L; Moore, Luiza L; Tullett, Mark M; Wong, Kim K; Ferreira, Ingrid I; Gómez, Julia M Martínez JMM; Levesque, Mitchell M; Gallagher, Ferdia A FA; Jiménez-Sánchez, Alejandro A; Riva, Laura L; Miller, Martin L ML; Allinson, Kieren K; Campbell, Peter J PJ; Corrie, Pippa P; Wedge, David C DC; Adams, David J DJ
Publication Date: 2020-08-27

Variant appearance in text: BRAF: 1798_1799delGT
PubMed Link: 32855398
Variant Present in the following documents:
  • Main text
  • 41467_2020_Article_18060.pdf
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Detection of BRAF Mutations Using a Fully Automated Platform and Comparison with High Resolution Melting, Real-Time Allele Specific Amplification, Immunohistochemistry and Next Generation Sequencing Assays, for Patients with Metastatic Melanoma.

Plos One
Harlé, Alexandre A; Salleron, Julia J; Franczak, Claire C; Dubois, Cindy C; Filhine-Tressarieu, Pierre P; Leroux, Agnès A; Merlin, Jean-Louis JL
Publication Date: 2016

Variant appearance in text: BRAF: 1799_1800del
PubMed Link: 27111917
Variant Present in the following documents:
  • pone.0153576.pdf
View BVdb publication page