Varaico: Literature-Extracted Genetic Variants

Gene:BRCA1
Variant:p.S1655A
Back to variants list

BRCA1

NM_007294.4:p.S1655A

Associated Papers

The BRCA1- RAD51 Axis Regulates SCAI/REV3 Dependent Replication Fork Maintenance.

Unterseher C et al.

Biorxiv : the Preprint Server for Biology, 2025

Triple-Action Therapy: Combining Machine Learning, Docking, and Dynamics to Combat BRCA1-Mutated Breast Cancer.

Zainulabidin AA et al.

Molecular Biotechnology, 2025

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 › BRCT1_ABX

ACMG/AMP interpretation of BRCA1 missense variants: Structure-informed scores add evidence strength granularity to the PP3/BP4 computational evidence.

Ramadane-Morchadi L et al.

American Journal of Human Genetics, 2025

40233743 (PubMed )
Supplement: mmc2.xlsx › Hoja1

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-2.xlsx › TableS1

BLM and BRCA1-BARD1 coordinate complementary mechanisms of joint DNA molecule resolution.

Tsukada K et al.

Molecular Cell, 2024

Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.

Qin Z et al.

International Journal of Cancer, 2023

36385461 (PubMed )
Supplement: IJC-152-1159-s003.xlsx › Sheet1

The BRCA1 BRCT promotes antisense RNA production and double-stranded RNA formation to suppress ribosomal R-loops.

Chang CW et al.

Proceedings of the National Academy of Sciences of the United States of America, 2022

Variomes: a high recall search engine to support the curation of genomic variants.

Pasche E et al.

Bioinformatics (oxford, England), 2022

35274687 (PubMed )
Supplement: btac146_supplementary_data.pdf

Erratum: Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome.

Unknown Author

Frontiers in Oncology, 2022

Two redundant ubiquitin-dependent pathways of BRCA1 localization to DNA damage sites.

Sherker A et al.

Embo Reports, 2021

Towards a New, Endophenotype-Based Strategy for Pathogenicity Prediction in BRCA1 and BRCA2: In Silico Modeling of the Outcome of HDR/SGE Assays for Missense Variants.

Özkan S et al.

International Journal of Molecular Sciences, 2021

34207612 (PubMed )
Supplement: ijms-22-06226-s001.zip › SUPP_FIGURES_TABLES › SupplementaryTable4.xlsx › supp_table4

Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome.

Fanale D et al.

Frontiers in Oncology, 2021

Classification of VUS and unclassified variants in BRCA1 BRCT repeats by molecular dynamics simulation.

Sinha S et al.

Computational and Structural Biotechnology Journal, 2020

CSB interacts with BRCA1 in late S/G2 to promote MRN- and CtIP-mediated DNA end resection.

Batenburg NL et al.

Nucleic Acids Research, 2019

Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk.

Petitalot A et al.

Molecular Cancer Research : Mcr, 2019

Human Rad52 Promotes XPG-Mediated R-loop Processing to Initiate Transcription-Associated Homologous Recombination Repair.

Yasuhara T et al.

Cell, 2018

Targeting Phosphopeptide Recognition by the Human BRCA1 Tandem BRCT Domain to Interrupt BRCA1-Dependent Signaling.

Periasamy J et al.

Cell Chemical Biology, 2018

And-1 coordinates with CtIP for efficient homologous recombination and DNA damage checkpoint maintenance.

Chen Y et al.

Nucleic Acids Research, 2017

Peptide library approach to uncover phosphomimetic inhibitors of the BRCA1 C-terminal domain.

White ER et al.

Acs Chemical Biology, 2015

Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations.

Martelotto LG et al.

Genome Biology, 2014

25348012 (PubMed )
Supplement: 13059_2014_484_MOESM2_ESM.xlsx › Additional_file_2

Function of BRCA1 in the DNA damage response is mediated by ADP-ribosylation.

Li M et al.

Cancer Cell, 2013

A cell cycle-dependent regulatory circuit composed of 53BP1-RIF1 and BRCA1-CtIP controls DNA repair pathway choice.

Escribano-Díaz C et al.

Molecular Cell, 2013

BRCT domains: phosphopeptide binding and signaling modules.

Rodriguez MC et al.

Frontiers in Bioscience : a Journal and Virtual Library, 2008

Structural basis of BACH1 phosphopeptide recognition by BRCA1 tandem BRCT domains.

Botuyan MV et al.

Structure (london, England : 1993), 2004

Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer.

Clapperton JA et al.

Nature Structural & Molecular Biology, 2004

Structural basis of phosphopeptide recognition by the BRCT domain of BRCA1.

Williams RS et al.

Nature Structural & Molecular Biology, 2004

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."