List of variants in gene BRIP1 reported by German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1629-3T>C	rs587780828	0.00006
NM_032043.3(BRIP1):c.1741C>T (p.Arg581Ter)	rs780020495	0.00002
NM_032043.3(BRIP1):c.1141-7_1141-3del	rs1060501744
NM_032043.3(BRIP1):c.1941G>C (p.Trp647Cys)	rs786202760
NM_032043.3(BRIP1):c.2258-1G>A	rs1064793887
NM_032043.3(BRIP1):c.2379G>T (p.Gln793His)	rs1567779336

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.