BRCA1 c.3758_3759del ;(p.S1253*)

Variant ID: 17-41243788-TAG-T

NM_007294.3(BRCA1):c.3758_3759del;(p.S1253*)

This variant was identified in 11 publications

View GRCh38 version.




Publications:


Whole-exome Sequencing of Nigerian Prostate Tumors from the Prostate Cancer Transatlantic Consortium (CaPTC) Reveals DNA Repair Genes Associated with African Ancestry.

Cancer Research Communications
White, Jason A JA; Kaninjing, Ernest T ET; Adeniji, Kayode A KA; Jibrin, Paul P; Obafunwa, John O JO; Ogo, Chidiebere N CN; Mohammed, Faruk F; Popoola, Ademola A; Fatiregun, Omolara A OA; Oluwole, Olabode P OP; Karanam, Balasubramanyam B; Elhussin, Isra I; Ambs, Stefan S; Tang, Wei W; Davis, Melissa M; Polak, Paz P; Campbell, Moray J MJ; Brignole, Kathryn R KR; Rotimi, Solomon O SO; Dean-Colomb, Windy W; Odedina, Folake T FT; Martin, Damali N DN; Yates, Clayton C
Publication Date: 2022-09

Variant appearance in text: BRCA1: 3758_3759del; Ser1253fs; rs1555587135
PubMed Link: 36922933
Variant Present in the following documents:
  • crc-22-0136-s01.xlsx, sheet 1
View BVdb publication page



Effect of BRCA1/2 Mutational Status on Survival Outcomes According to Secondary Cytoreductive Surgery and Maintenance Therapy in Platinum-Sensitive Relapsed Ovarian Cancer: A Real-World Evidence Study.

Cancer Research And Treatment
Kim, Se Ik SI; Lim, Hyunji H; Kim, Hee Seung HS; Chung, Hyun Hoon HH; Kim, Jae-Weon JW; Park, Noh Hyun NH; Song, Yong-Sang YS; Lee, Maria M
Publication Date: 2022-07-19

Variant appearance in text: BRCA1: 3758_3759del; Ser1253Ter
PubMed Link: 35879854
Variant Present in the following documents:
  • crt-2022-232-S1-Table.pdf
View BVdb publication page



A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: BRCA1: 3758_3759delCT; Ser1253Terfs
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 7
View BVdb publication page



Germline variants in hereditary breast cancer genes are associated with early age at diagnosis and family history in Guatemalan breast cancer.

Breast Cancer Research And Treatment
Ren, Megan M; Orozco, Anali A; Shao, Kang K; Albanez, Anaseidy A; Ortiz, Jeremy J; Cao, Boyang B; Wang, Lusheng L; Barreda, Lilian L; Alvarez, Christian S CS; Garland, Lisa L; Wu, Dongjing D; Chung, Charles C CC; Wang, Jiahui J; Frone, Megan M; Ralon, Sergio S; Argueta, Victor V; Orozco, Roberto R; Gharzouzi, Eduardo E; Dean, Michael M
Publication Date: 2021-09

Variant appearance in text: N/A
PubMed Link: 34196900
Variant Present in the following documents:
View BVdb publication page



Comprehensive analysis of serum tumor markers and BRCA1/2 germline mutations in Chinese ovarian cancer patients.

Molecular Genetics & Genomic Medicine
Deng, Hongyu H; Chen, Ming M; Guo, Xinwu X; Heng, Jianfu J; Xu, Xunxun X; Peng, Limin L; Jiang, Hui H; Li, Guoli G; Day, Julia X JX; Li, Jinliang J; Shan, Dongyong D; Li, Yinghua Y; Zhou, Yanjie Y; Liu, Bin B; Dai, Lizhong L; Wang, Xiaochun X; Wang, Jun J
Publication Date: 2019-06

Variant appearance in text: BRCA1: 3758_3759delCT; S1253fs
PubMed Link: 30972954
Variant Present in the following documents:
  • Main text
  • MGG3-7-e672-s001.pdf
  • MGG3-7-e672.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: BRCA1: 3758_3759delCT
PubMed Link: 30702160
Variant Present in the following documents:
  • IJC-145-962-s007.xlsx, sheet 3
View BVdb publication page



BRCA1 and BRCA2 mutations and clinical interpretation in 398 ovarian cancer patients: comparison with breast cancer variants in a similar population.

Human Genomics
Cardoso, Florencia C FC; Goncalves, Susana S; Mele, Pablo G PG; Liria, Natalia C NC; Sganga, Leonardo L; Diaz Perez, Ignacio I; Podesta, Ernesto J EJ; Solano, Angela R AR
Publication Date: 2018-08-13

Variant appearance in text: BRCA1: 3758_3759delCT; Ser1253*
PubMed Link: 30103829
Variant Present in the following documents:
  • Main text
  • 40246_2018_Article_171.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: BRCA1: 3758_3759delCT; Ser1253*
PubMed Link: 28947987
Variant Present in the following documents:
  • Main text
  • oncotarget-08-60487.pdf
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: BRCA1: 3758_3759delCT; Ser1253*
PubMed Link: 28127413
Variant Present in the following documents:
  • Main text
  • 13053_2017_Article_63.pdf
View BVdb publication page



The spectrum of BRCA1 and BRCA2 alleles in Latin America and the Caribbean: a clinical perspective.

Breast Cancer Research And Treatment
Dutil, Julie J; Golubeva, Volha A VA; Pacheco-Torres, Alba L AL; Diaz-Zabala, Hector J HJ; Matta, Jaime L JL; Monteiro, Alvaro N AN
Publication Date: 2015-12

Variant appearance in text: BRCA1: 3758_3759delCT
PubMed Link: 26564481
Variant Present in the following documents:
  • 10549_2015_3629_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin.

Springerplus
Solano, Angela Rosaria AR; Aceto, Gitana Maria GM; Delettieres, Dreanina D; Veschi, Serena S; Neuman, Maria Isabel MI; Alonso, Eduardo E; Chialina, Sergio S; Chacón, Reinaldo Daniel RD; Renato, Mariani-Costantini MC; Podestá, Ernesto Jorge EJ
Publication Date: 2012

Variant appearance in text: BRCA1: 3758_3759delCT; S1253X
PubMed Link: 23961350
Variant Present in the following documents:
  • Main text
  • 40064_2012_Article_24.pdf
View BVdb publication page