BRAF c.1952C>T ;(p.T651I)

Variant ID: 7-140449127-G-A


This variant was identified in 1 publication

View GRCh38 version.


A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.

Plos Computational Biology
Sun, James X JX; He, Yuting Y; Sanford, Eric E; Montesion, Meagan M; Frampton, Garrett M GM; Vignot, St├ęphane S; Soria, Jean-Charles JC; Ross, Jeffrey S JS; Miller, Vincent A VA; Stephens, Phil J PJ; Lipson, Doron D; Yelensky, Roman R
Publication Date: 2018-02

Variant appearance in text: BRAF: 1952C>T
PubMed Link: 29415044
Variant Present in the following documents:
  • pcbi.1005965.s010.pdf
View BVdb publication page