NF1 c.2826C>T ;(p.S942=)

Variant ID: 17-29556459-C-T

NM_001042492.2(NF1):c.2826C>T;(p.S942=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Molecular features of tumor-derived genetic alterations in circulating cell-free DNA in virtue of autopsy analysis.

Scientific Reports
Koba, Hayato H; Kimura, Hideharu H; Yoneda, Taro T; Sone, Takashi T; Ohkura, Noriyuki N; Hara, Johsuke J; Hosomichi, Kazuyoshi K; Tajima, Atsushi A; Kasahara, Kazuo K
Publication Date: 2021-04-16

Variant appearance in text: NF1: 2826C>T
PubMed Link: 33863951
Variant Present in the following documents:
  • 41598_2021_Article_87094.pdf
View BVdb publication page



Genetic hierarchy and temporal variegation in the clonal history of acute myeloid leukaemia.

Nature Communications
Hirsch, Pierre P; Zhang, Yanyan Y; Tang, Ruoping R; Joulin, Virginie V; Boutroux, Hélène H; Pronier, Elodie E; Moatti, Hannah H; Flandrin, Pascale P; Marzac, Christophe C; Bories, Dominique D; Fava, Fanny F; Mokrani, Hayat H; Betems, Aline A; Lorre, Florence F; Favier, Rémi R; Féger, Frédéric F; Mohty, Mohamad M; Douay, Luc L; Legrand, Ollivier O; Bilhou-Nabera, Chrystèle C; Louache, Fawzia F; Delhommeau, François F
Publication Date: 2016-08-18

Variant appearance in text: NF1: 2826C>T
PubMed Link: 27534895
Variant Present in the following documents:
  • ncomms12475-s3.xlsx, sheet 1
  • ncomms12475-s2.xlsx, sheet 1
View BVdb publication page