EPHB2 c.811+3684T>G

Variant ID: 1-23115253-T-G

NM_017449.3(EPHB2):c.811+3684T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A somatic reference standard for cancer genome sequencing.

Scientific Reports
Craig, David W DW; Nasser, Sara S; Corbett, Richard R; Chan, Simon K SK; Murray, Lisa L; Legendre, Christophe C; Tembe, Waibhav W; Adkins, Jonathan J; Kim, Nancy N; Wong, Shukmei S; Baker, Angela A; Enriquez, Daniel D; Pond, Stephanie S; Pleasance, Erin E; Mungall, Andrew J AJ; Moore, Richard A RA; McDaniel, Timothy T; Ma, Yussanne Y; Jones, Steven J M SJ; Marra, Marco A MA; Carpten, John D JD; Liang, Winnie S WS
Publication Date: 2016-04-20

Variant appearance in text: EPHB2: 811+3684T>G
PubMed Link: 27094764
Variant Present in the following documents:
  • srep24607-s2.xls, sheet 1
View BVdb publication page