ATM c.1402_1406del ;(p.K468Vfs*17)

Variant ID: 11-108121594-CAAGAG-C

NM_000051.3(ATM):c.1402_1406del;(p.K468Vfs*17)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pancreatic cancer as a sentinel for hereditary cancer predisposition.

Bmc Cancer
Young, Erin L EL; Thompson, Bryony A BA; Neklason, Deborah W DW; Firpo, Matthew A MA; Werner, Theresa T; Bell, Russell R; Berger, Justin J; Fraser, Alison A; Gammon, Amanda A; Koptiuch, Cathryn C; Kohlmann, Wendy K WK; Neumayer, Leigh L; Goldgar, David E DE; Mulvihill, Sean J SJ; Cannon-Albright, Lisa A LA; Tavtigian, Sean V SV
Publication Date: 2018-06-27

Variant appearance in text: ATM: 1402_1406delAAGAG; K468Vfs*17
PubMed Link: 29945567
Variant Present in the following documents:
  • Main text
  • 12885_2018_4573_MOESM1_ESM.xlsx, sheet 2
  • 12885_2018_Article_4573.pdf
View BVdb publication page