ClinVar Miner

List of variants in gene BARD1 studied for Breast and/or ovarian cancer

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys) rs35306212 0.00455
NM_000465.4(BARD1):c.1977A>G (p.Arg659=) rs147215925 0.00230
NM_000465.4(BARD1):c.620A>G (p.Lys207Arg) rs34969857 0.00218
NM_000465.4(BARD1):c.33G>T (p.Gln11His) rs143914387 0.00176
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn) rs142155101 0.00153
NM_000465.4(BARD1):c.144G>A (p.Leu48=) rs151168457 0.00050
NM_000465.4(BARD1):c.215+12C>T rs373816832 0.00049
NM_000465.4(BARD1):c.668A>G (p.Glu223Gly) rs145009419 0.00024
NM_000465.4(BARD1):c.1347A>G (p.Gln449=) rs373257776 0.00021
NM_000465.4(BARD1):c.1835A>T (p.Asp612Val) rs201140528 0.00011
NM_000465.4(BARD1):c.2002-11C>T rs187240320 0.00010
NM_000465.4(BARD1):c.127C>A (p.Arg43Ser) rs752871324 0.00006
NM_000465.4(BARD1):c.1793C>A (p.Thr598Asn) rs376256852 0.00006
NM_000465.4(BARD1):c.716T>A (p.Leu239Gln) rs200359745 0.00006
NM_000465.4(BARD1):c.1877A>G (p.Asn626Ser) rs587781443 0.00004
NM_000465.4(BARD1):c.783A>G (p.Leu261=) rs201862973 0.00004
NM_000465.4(BARD1):c.1690C>T (p.Gln564Ter) rs587780021 0.00003
NM_000465.4(BARD1):c.2252G>A (p.Arg751Gln) rs587782246 0.00003
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn) rs369561166 0.00003
NM_000465.4(BARD1):c.159T>C (p.Cys53=) rs201708813 0.00002
NM_000465.4(BARD1):c.1016G>A (p.Ser339Asn) rs201261729 0.00001
NM_000465.4(BARD1):c.161C>G (p.Thr54Ser) rs879253878 0.00001
NM_000465.4(BARD1):c.334C>T (p.Arg112Ter) rs758972589 0.00001
NM_000465.4(BARD1):c.*8A>G
NM_000465.4(BARD1):c.1568+6T>A rs1553619192
NM_000465.4(BARD1):c.157T>G (p.Cys53Gly) rs1354779388
NM_000465.4(BARD1):c.1810+2T>G rs1234033325
NM_000465.4(BARD1):c.1944A>G (p.Glu648=)
NM_000465.4(BARD1):c.2091A>T (p.Ala697=) rs786201573
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly) rs76744638
NM_000465.4(BARD1):c.2300_2301del (p.Val767fs) rs750413473
NM_000465.4(BARD1):c.297A>G (p.Arg99=) rs878854010
NM_000465.4(BARD1):c.505A>G (p.Ile169Val) rs765494437
NM_000465.4(BARD1):c.72C>A (p.Pro24=) rs2106171466
NM_000465.4(BARD1):c.941T>C (p.Leu314Ser) rs199857391

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.