Varaico: Literature-Extracted Genetic Variants

Gene:BRCA2
Variant:p.Y1894_E1895insFs
Back to variants list

BRCA2

NM_000059.4:p.Y1894_E1895insFs

Associated Papers

Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa.

ElBiad O et al.

Bmc Cancer, 2022

BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with hereditary breast cancer.

Wang J et al.

Molecular Genetics & Genomic Medicine, 2020

BRCA1/BRCA2 Mutations Shaped by Ancient Consanguinity Practice in Southern Mediterranean Populations

Belaiba F et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2018

Genetics of breast cancer in African populations: a literature review.

Abbad A et al.

Global Health, Epidemiology and Genomics, 2018

Monoallelic characteristic-bearing heterozygous L1053X in BRCA2 gene among Sudanese women with breast cancer.

Elimam AA et al.

Bmc Medical Genetics, 2017

Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families.

Riahi A et al.

Breast Cancer (tokyo, Japan), 2017

Contribution of the BRCA1 and BRCA2 mutations to breast cancer in Tunisia.

Troudi W et al.

Journal of Human Genetics, 2007

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."