Varaico: Literature-Extracted Genetic Variants

Gene:BRCA1
Variant:p.W1815G
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BRCA1

NM_007294.4:p.W1815G

Associated Papers

Profiling BRCA1-BRCT interactions and their functional relevance at amino acid resolution.

Mangkusaputra V et al.

Nucleic Acids Research, 2025

40966517 (PubMed )
Supplement: gkaf848_supplemental_files.zip › Sup_table_2___ABX_CtIP_complete_count_and_scores.xlsx › BRCT3_ABX

Genetic screening of FFPE breast cancer biopsies for the BRCA1-185delAG mutation in Trinidad and Tobago.

Abrahim SC et al.

Revista Panamericana De Salud Publica = Pan American Journal of Public Health, 2025

Protein-folding chaperones predict structure-function relationships and cancer risk in BRCA1 mutation carriers.

Gracia B et al.

Cell Reports, 2024

38368609 (PubMed )
Supplement: NIHMS1970903-supplement-6.xlsx › Table_S5

Founder vs. non-founder BRCA1/2 pathogenic alleles: the analysis of Belarusian breast and ovarian cancer patients and review of other studies on ethnically homogenous populations.

Yanus GA et al.

Familial Cancer, 2023

BRCA1 and Breast Cancer: Molecular Mechanisms and Therapeutic Strategies.

Fu X et al.

Frontiers in Cell and Developmental Biology, 2022

35300412 (PubMed )
Supplement: DataSheet1.xlsx › Sheet1

Short report: Follow-up of Bahamian women with a BRCA1 or BRCA2 mutation.

Narod SA et al.

Molecular Genetics & Genomic Medicine, 2018

Prevalence of founder mutations in the BRCA1 and BRCA2 genes among unaffected women from the Bahamas.

Trottier M et al.

Clinical Genetics, 2016

A high frequency of BRCA mutations in young black women with breast cancer residing in Florida.

Pal T et al.

Cancer, 2015

The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas.

Akbari MR et al.

Clinical Genetics, 2014

A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.

Karami F et al.

Biomed Research International, 2013

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).

Lindor NM et al.

Human Mutation, 2012

DNA damage and breast cancer.

Davis JD et al.

World Journal of Clinical Oncology, 2011

Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer.

Gonzalez-Angulo AM et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2011

A high prevalence of BRCA1 mutations among breast cancer patients from the Bahamas.

Donenberg T et al.

Breast Cancer Research and Treatment, 2011

Characterisation of gene expression profiles of yeast cells expressing BRCA1 missense variants.

Di Cecco L et al.

European Journal of Cancer (oxford, England : 1990), 2009

Classification of BRCA1 missense variants of unknown clinical significance.

Phelan CM et al.

Journal of Medical Genetics, 2005

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.

Eng C et al.

Journal of Medical Genetics, 2001

BRCA1 mutation update and analysis.

Grade K et al.

Journal of Cancer Research and Clinical Oncology, 1996

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