FLT4 c.1911C>G ;(p.S637R)

Variant ID: 5-180048651-G-C

NM_182925.4(FLT4):c.1911C>G;(p.S637R)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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, Stéphane 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: rs148898412
PubMed Link: 29415044
Variant Present in the following documents:
  • pcbi.1005965.s007.pdf
View BVdb publication page



Prospective comprehensive genomic profiling of advanced gastric carcinoma cases reveals frequent clinically relevant genomic alterations and new routes for targeted therapies.

The Oncologist
Ali, Siraj M SM; Sanford, Eric M EM; Klempner, Samuel J SJ; Rubinson, Douglas A DA; Wang, Kai K; Palma, Norma A NA; Chmielecki, Juliann J; Yelensky, Roman R; Palmer, Gary A GA; Morosini, Deborah D; Lipson, Doron D; Catenacci, Daniel V DV; Braiteh, Fadi F; Erlich, Rachel R; Stephens, Philip J PJ; Ross, Jeffrey S JS; Ou, Sai-Hong Ignatius SH; Miller, Vincent A VA
Publication Date: 2015-05

Variant appearance in text: VEGFR3: S637R
PubMed Link: 25882375
Variant Present in the following documents:
  • Main text
View BVdb publication page