Publications:

Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows.

Bmc Medical Genomics

Sobahy, Turki M TM; Tashkandi, Ghassan G; Bahussain, Donya D; Al-Harbi, Raneem R

Publication Date: 2022-04-25

Variant appearance in text: NF1: 3592G>T; E1198*

PubMed Link: 35468810

Variant Present in the following documents:

• 12920_2022_1235_MOESM4_ESM.xlsx, sheet 1

View BVdb publication page

NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomas.

Cancer Medicine

Tlemsani, Camille C; Pécuchet, Nicolas N; Gruber, Aurelia A; Laurendeau, Ingrid I; Danel, Claire C; Riquet, Marc M; Le Pimpec-Barthes, Françoise F; Fabre, Elizabeth E; Mansuet-Lupo, Audrey A; Damotte, Diane D; Alifano, Marco M; Luscan, Armelle A; Rousseau, Benoit B; Vidaud, Dominique D; Varin, Jennifer J; Parfait, Beatrice B; Bieche, Ivan I; Leroy, Karen K; Laurent-Puig, Pierre P; Terris, Benoit B; Blons, Helene H; Vidaud, Michel M; Pasmant, Eric E

Publication Date: 2019-08

Variant appearance in text: NF1: 3592G>T; Glu1198*

PubMed Link: 31199580

Variant Present in the following documents:

• CAM4-8-4330-s001.pdf

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A Landscape of Pharmacogenomic Interactions in Cancer.

Cell

Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ

Publication Date: 2016-07-28

Variant appearance in text: NF1: 3592G>T; E1198*

PubMed Link: 27397505

Variant Present in the following documents:

• mmc3.xlsx, sheet 2

View BVdb publication page