ATM c.2472_2478del ;(p.F825Kfs*9)

Variant ID: 11-108137898-GCATCCTT-G

NM_000051.3(ATM):c.2472_2478del;(p.F825Kfs*9)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The transfer of multigene panel testing for hereditary breast and ovarian cancer to healthcare: What are the implications for the management of patients and families?

Oncotarget
Eliade, Marie M; Skrzypski, Jeremy J; Baurand, Amandine A; Jacquot, Caroline C; Bertolone, Geoffrey G; Loustalot, Catherine C; Coutant, Charles C; Guy, France F; Fumoleau, Pierre P; Duffourd, Yannis Y; Arnould, Laurent L; Delignette, Alexandra A; Padéano, Marie-Martine MM; Lepage, Côme C; Raichon-Patru, Géraldine G; Boudrant, Axelle A; Bône-Lépinoy, Marie-Christine MC; Villing, Anne-Laure AL; Charpin, Aurélie A; Peignaux, Karine K; Chevrier, Sandy S; Vegran, Frédérique F; Ghiringhelli, François F; Boidot, Romain R; Sevenet, Nicolas N; Lizard, Sarab S; Faivre, Laurence L
Publication Date: 2017-01-10

Variant appearance in text: ATM: 2472_2478del; Phe825LysfsX9
PubMed Link: 27779110
Variant Present in the following documents:
  • Main text
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