BRAF c.683A>T ;(p.E228V)

Variant ID: 7-140507788-T-A

NM_004333.4(BRAF):c.683A>T;(p.E228V)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Plos Computational Biology
Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR
Publication Date: 2019-04

Variant appearance in text: BRAF: E228V
PubMed Link: 31034466
Variant Present in the following documents:
  • pcbi.1006981.s010.xlsx, sheet 1
View BVdb publication page



Cancer systems biology of TCGA SKCM: efficient detection of genomic drivers in melanoma.

Scientific Reports
Guan, Jian J; Gupta, Rohit R; Filipp, Fabian V FV
Publication Date: 2015-01-20

Variant appearance in text: BRAF: E228V
PubMed Link: 25600636
Variant Present in the following documents:
  • Main text
  • srep07857.pdf
View BVdb publication page



Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations.

Genome Biology
Martelotto, Luciano G LG; Ng, Charlotte Ky CK; De Filippo, Maria R MR; Zhang, Yan Y; Piscuoglio, Salvatore S; Lim, Raymond S RS; Shen, Ronglai R; Norton, Larry L; Reis-Filho, Jorge S JS; Weigelt, Britta B
Publication Date: 2014-10-28

Variant appearance in text: BRAF: E228V
PubMed Link: 25348012
Variant Present in the following documents:
  • 13059_2014_484_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page