List of variants in gene BRCA1 reported as likely pathogenic for Malignant tumor of breast

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.4868C>G (p.Ala1623Gly)	rs80356862
NM_007294.4(BRCA1):c.4986+3G>C	rs80358023
NM_007294.4(BRCA1):c.5089T>C (p.Cys1697Arg)	rs80356993
NM_007294.4(BRCA1):c.5165C>T (p.Ser1722Phe)	rs80357104
NM_007294.4(BRCA1):c.5216A>G (p.Asp1739Gly)	rs80357227
NM_007294.4(BRCA1):c.5309G>T (p.Gly1770Val)	rs863224765
NM_007294.4(BRCA1):c.5509T>G (p.Trp1837Gly)	rs80356959

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.