Paper Details

Paper Title

Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots".

Paper Journal Title

Genet Med

Paper Citation Count

Paper Publication Year

2020

Bio Mention

BRCA1, BRCA1 and, BRCA1 and BRCA2 "coldspots, BRCA1 exon, BRCA1 exon 11, BRCA2, BRCA2 coldspots, BRCA2 exons, BRCA2 exons 10 and, PM1, PP2, coding sequence, coldspots, exon 11, exons 10-11, functional domains

Mesh Descriptor

Author Name	Affiliation
Brian H Shirts	University of Washington
Tom Walsh	University of Washington
Tom Walsh	University of Washington
Mary-Claire King	University of Washington
Mary-Claire King	University of Washington
Mary-Claire King	University of Washington
Mary-Claire King	University of Washington
Douglas M Fowler	University of Washington
Colin C Pritchard	University of Washington

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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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