List of variants in gene BRCA1, LOC111589215 studied for Hereditary breast ovarian cancer syndrome

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: 35

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-192T>C	rs113323025	0.00510
NM_007294.4(BRCA1):c.-86C>T	rs143160357	0.00077
NM_007294.4(BRCA1):c.-20+11C>T	rs273898672	0.00042
NM_007294.4(BRCA1):c.-125C>T	rs148196794	0.00017
NM_007294.4(BRCA1):c.-20+1G>C	rs769633464	0.00001
NC_000017.10:g.(?_41276014)_(41277500_?)dup
NC_000017.10:g.(?_41277288)_(41277500_?)dup
NC_000017.11:g.(?_43123997)_(43125483_?)del
NC_000017.11:g.43125428G>A
NC_000017.11:g.43125428G>C
NM_007294.4(BRCA1):c.-109A>T	rs886052977
NM_007294.4(BRCA1):c.-20+10T>A
NM_007294.4(BRCA1):c.-20+10T>C
NM_007294.4(BRCA1):c.-20+125A>C	rs1238736956
NM_007294.4(BRCA1):c.-20+12C>T	rs2154579973
NM_007294.4(BRCA1):c.-20+13C>G	rs770368390
NM_007294.4(BRCA1):c.-20+13C>T	rs770368390
NM_007294.4(BRCA1):c.-20+14G>A	rs2154579967
NM_007294.4(BRCA1):c.-20+14G>T	rs2154579967
NM_007294.4(BRCA1):c.-20+15G>C	rs2154579965
NM_007294.4(BRCA1):c.-20+16G>A	rs1358783922
NM_007294.4(BRCA1):c.-20+16G>C	rs1358783922
NM_007294.4(BRCA1):c.-20+17A>G	rs2154579960
NM_007294.4(BRCA1):c.-20+19A>C
NM_007294.4(BRCA1):c.-20+20G>C	rs2154579954
NM_007294.4(BRCA1):c.-20+2T>C	rs1567824383
NM_007294.4(BRCA1):c.-20+2dup
NM_007294.4(BRCA1):c.-20+386A>G	rs2154579506
NM_007294.4(BRCA1):c.-20+3A>G	rs1064795882
NM_007294.4(BRCA1):c.-20+3A>T	rs1064795882
NM_007294.4(BRCA1):c.-20+4G>C	rs745476489
NM_007294.4(BRCA1):c.-20+5T>C	rs1057524628
NM_007294.4(BRCA1):c.-20+6A>G
NM_007294.4(BRCA1):c.-20+9G>A
NM_007294.4(BRCA1):c.-70A>G

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.