Varaico: Literature-Extracted Genetic Variants

Gene:BRCA2
Variant:p.Q853insFs
Back to variants list

BRCA2

NM_000059.4:p.Q853insFs

Associated Papers

Mutational spectrum of DNA damage and mismatch repair genes in prostate cancer.

Bugoye FC et al.

Frontiers in Genetics, 2023

The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families.

Fierheller CT et al.

Cancers, 2021

34298626 (PubMed )
Supplement: cancers-13-03406-s001.zip › cancers-1247507-supplementary › Supplementary_Tables_V12_18062021_REFs.xlsx › Supp_Table_2

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

Bhaskaran SP et al.

International Journal of Cancer, 2019

30702160 (PubMed )
Supplement: IJC-145-962-s007.xlsx › CIMBA

The role of BRCA1 and BRCA2 in prostate cancer.

Li D et al.

Frontiers in Bioscience (landmark Edition), 2013

Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.

Castro E et al.

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology, 2013

Prostate cancer in BRCA2 germline mutation carriers is associated with poorer prognosis.

Edwards SM et al.

British Journal of Cancer, 2010

Prostate cancer in male BRCA1 and BRCA2 mutation carriers has a more aggressive phenotype.

Mitra A et al.

British Journal of Cancer, 2008

Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer.

Simard J et al.

Journal of Medical Genetics, 2007

Predictors of occult neoplasia in women undergoing risk-reducing salpingo-oophorectomy.

Lamb JD et al.

American Journal of Obstetrics and Gynecology, 2006

Two percent of men with early-onset prostate cancer harbor germline mutations in the BRCA2 gene.

Edwards SM et al.

American Journal of Human Genetics, 2003

Hereditary ovarian cancer resulting from a non-ovarian cancer cluster region (OCCR) BRCA2 mutation: is the OCCR useful clinically?

Al-Saffar M et al.

Journal of Medical Genetics, 2002

[BRCA2 gene mutation detection in hereditary ovarian cancer tissues].

Qiao Y et al.

Zhonghua Fu Chan Ke Za Zhi, 2002

Unexpected gynecologic neoplasms in patients with proven or suspected BRCA-1 or -2 mutations: implications for gross examination, cytology, and clinical follow-up.

Agoff SN et al.

The American Journal of Surgical Pathology, 2002

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."