Paper Details

Paper Title

Novel candidates of pathogenic variants of the BRCA1 and BRCA2 genes from a dataset of 3,552 Japanese whole genomes (3.5KJPNv2).

Paper Journal Title

PLoS One

Paper Citation Count

Paper Publication Year

2021

Bio Mention

BRCA genes, BRCA1, BRCA1 and BRCA2 genes, BRCA1/2, BRCA2 genes, HBOC, HBOC gene, HBOC gene variants, HBOC genes, LP variants, P and, P and LP variants, breast and ovarian cancers, cancer, cancers, hereditary breast and ovarian cancer syndrome, minor, participants, patients, whole-genome sequences

Mesh Descriptor

Author Name	Affiliation
Soichi Ogishima	Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University
Soichi Ogishima	Tohoku University
Kengo Kinoshita	Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University
Kengo Kinoshita	Tohoku University
Kengo Kinoshita	Tohoku University
Kengo Kinoshita	Miyagi Cancer Center Research Institute
Kengo Kinoshita	Institute of Development, Tohoku University

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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