BRAF c.1795A>T ;(p.T599S)

Variant ID: 7-140453140-T-A

NM_004333.4(BRAF):c.1795A>T;(p.T599S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples.

Plos One
Betge, Johannes J; Kerr, Grainne G; Miersch, Thilo T; Leible, Svenja S; Erdmann, Gerrit G; Galata, Christian L CL; Zhan, Tianzuo T; Gaiser, Timo T; Post, Stefan S; Ebert, Matthias P MP; Horisberger, Karoline K; Boutros, Michael M
Publication Date: 2015

Variant appearance in text: BRAF: T599S
PubMed Link: 26010451
Variant Present in the following documents:
  • pone.0127146.s014.xlsx, sheet 3
  • pone.0127146.s013.xlsx, sheet 3
View BVdb publication page



Next generation sequencing of exceptional responders with BRAF-mutant melanoma: implications for sensitivity and resistance.

Bmc Cancer
Wheler, Jennifer J; Yelensky, Roman R; Falchook, Gerald G; Kim, Kevin B KB; Hwu, Patrick P; Tsimberidou, Apostolia M AM; Stephens, Philip J PJ; Hong, David D; Cronin, Maureen T MT; Kurzrock, Razelle R
Publication Date: 2015-02-18

Variant appearance in text: BRAF: T599S
PubMed Link: 25886620
Variant Present in the following documents:
  • Main text
  • 12885_2015_Article_1029.pdf
View BVdb publication page