BRCA2 c.66_67del ;(p.D23Ffs*7)

Variant ID: 13-32890663-CAG-C

NM_000059.3(BRCA2):c.66_67del;(p.D23Ffs*7)

This variant was identified in 11 publications

View GRCh38 version.




Publications:


Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location.

Genes
Sekine, Masayuki M; Nishino, Koji K; Enomoto, Takayuki T
Publication Date: 2021-07-08

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 34356066
Variant Present in the following documents:
  • genes-12-01050.pdf
View BVdb publication page



Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy.

Genes
Urbina-Jara, Laura Keren LK; Rojas-Martinez, Augusto A; Martinez-Ledesma, Emmanuel E; Aguilar, Dione D; Villarreal-Garza, Cynthia C; Ortiz-Lopez, Rocio R
Publication Date: 2019-10-10

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 31658756
Variant Present in the following documents:
  • Main text
  • genes-10-00786.pdf
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A Multi-Center Study of BRCA1 and BRCA2 Germline Mutations in Mexican-Mestizo Breast Cancer Families Reveals Mutations Unreported in Latin American Population.

Cancers
Millan Catalan, Oliver O; Campos-Parra, Alma D AD; Vázquez-Romo, Rafael R; Cantú de León, David D; Jacobo-Herrera, Nadia N; Morales-González, Fermín F; López-Camarillo, César C; Rodríguez-Dorantes, Mauricio M; López-Urrutia, Eduardo E; Pérez-Plasencia, Carlos C
Publication Date: 2019-08-26

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 31454914
Variant Present in the following documents:
  • cancers-11-01246.pdf
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Estrogen Receptor Status Oppositely Modifies Breast Cancer Prognosis in BRCA1/BRCA2 Mutation Carriers Versus Non-Carriers.

Cancers
Vocka, Michal M; Zimovjanova, Martina M; Bielcikova, Zuzana Z; Tesarova, Petra P; Petruzelka, Lubos L; Mateju, Martin M; Krizova, Ludmila L; Kotlas, Jaroslav J; Soukupova, Jana J; Janatova, Marketa M; Zemankova, Petra P; Kleiblova, Petra P; Novotny, Jan J; Konopasek, Bohuslav B; Chodacka, Martina M; Brychta, Milan M; Sochor, Marek M; Smejkalova-Musilova, Denisa D; Cmejlova, Vlastimila V; Kozevnikovova, Renata R; Miskarova, Lenka L; Argalacsova, Sona S; Stolarova, Lenka L; Lhotova, Klara K; Borecka, Marianna M; Kleibl, Zdenek Z
Publication Date: 2019-05-28

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 31141992
Variant Present in the following documents:
  • cancers-11-00738-s001.pdf
View BVdb publication page



Germline variation in BRCA1/2 is highly ethnic-specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients.

International Journal Of Cancer
Bhaskaran, Shanmuga Priya SP; Chandratre, Khyati K; Gupta, Hemant H; Zhang, Li L; Wang, Xiaoyu X; Cui, Jian J; Kim, Yeong C YC; Sinha, Siddharth S; Jiang, Luhan L; Lu, Boya B; Wu, Xiaobing X; Qin, Zixin Z; Huang, Teng T; Wang, San Ming SM
Publication Date: 2019-08-15

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 30702160
Variant Present in the following documents:
  • IJC-145-962-s007.xlsx, sheet 3
View BVdb publication page



Double Heterozygosity for BRCA1 Pathogenic Variant and BRCA2 Polymorphic Stop Codon K3326X: A Case Report in a Southern Italian Family.

International Journal Of Molecular Sciences
Palmirotta, Raffaele R; Lovero, Domenica D; Stucci, Luigia Stefania LS; Silvestris, Erica E; Quaresmini, Davide D; Cardascia, Angela A; Silvestris, Franco F
Publication Date: 2018-01-18

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 29346284
Variant Present in the following documents:
  • Main text
  • ijms-19-00285.pdf
View BVdb publication page



Spectrum of BRCA1/2 variants in 940 patients from Argentina including novel, deleterious and recurrent germline mutations: impact on healthcare and clinical practice.

Oncotarget
Solano, Angela Rosaria AR; Cardoso, Florencia Cecilia FC; Romano, Vanesa V; Perazzo, Florencia F; Bas, Carlos C; Recondo, Gonzalo G; Santillan, Francisco Bernardo FB; Gonzalez, Eduardo E; Abalo, Eduardo E; Viniegra, María M; Michel, José Davalos JD; Nuñez, Lina María LM; Noblia, Cristina Maria CM; Mc Lean, Ignacio I; Canton, Enrique Diaz ED; Chacon, Reinaldo Daniel RD; Cortese, Gustavo G; Varela, Eduardo Beccar EB; Greco, Martín M; Barrientos, María Laura ML; Avila, Silvia Adela SA; Vuotto, Hector Daniel HD; Lorusso, Antonio A; Podesta, Ernesto Jorge EJ; Mando, Oscar Gaspar OG
Publication Date: 2017-09-01

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 28947987
Variant Present in the following documents:
  • Main text
View BVdb publication page



Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.

Hereditary Cancer In Clinical Practice
Cruz-Correa, Marcia M; Pérez-Mayoral, Julyann J; Dutil, Julie J; Echenique, Miguel M; Mosquera, Rafael R; Rivera-Román, Keila K; Umpierre, Sharee S; Rodriguez-Quilichini, Segundo S; Gonzalez-Pons, Maria M; Olivera, Myrta I MI; Pardo, Sherly S; ,
Publication Date: 2017

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 28127413
Variant Present in the following documents:
  • Main text
  • 13053_2017_Article_63.pdf
View BVdb publication page



Founder and Recurrent Mutations in BRCA1 and BRCA2 Genes in Latin American Countries: State of the Art and Literature Review.

The Oncologist
Ossa, Carlos Andrés CA; Torres, Diana D
Publication Date: 2016-07

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 27286788
Variant Present in the following documents:
  • Main text
View BVdb publication page



Development and Validation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Variants for the Clinical Laboratory.

Plos One
Strom, Charles M CM; Rivera, Steven S; Elzinga, Christopher C; Angeloni, Taraneh T; Rosenthal, Sun Hee SH; Goos-Root, Dana D; Siaw, Martin M; Platt, Jamie J; Braastadt, Cory C; Cheng, Linda L; Ross, David D; Sun, Weimin W
Publication Date: 2015

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 26295337
Variant Present in the following documents:
  • pone.0136419.pdf
View BVdb publication page



Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families.

International Journal Of Oncology
Novaković, Srdjan S; Milatović, Maša M; Cerkovnik, Petra P; Stegel, Vida V; Krajc, Mateja M; Hočevar, Marko M; Zgajnar, Janez J; Vakselj, Aleš A
Publication Date: 2012-11

Variant appearance in text: BRCA2: 66_67delAG
PubMed Link: 22923021
Variant Present in the following documents:
  • Main text
View BVdb publication page