Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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