ClinVar Miner

List of variants in gene BARD1 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1977A>G (p.Arg659=) rs147215925 0.00230
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.348T>C (p.His116=) rs139934362 0.00039
NM_000465.4(BARD1):c.1515G>T (p.Gly505=) rs139721211 0.00029
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.842C>T (p.Pro281Leu) rs367890377 0.00021
NM_000465.4(BARD1):c.57G>A (p.Glu19=) rs730881406 0.00019
NM_000465.4(BARD1):c.1554C>T (p.Ala518=) rs139612775 0.00015
NM_000465.4(BARD1):c.44G>T (p.Arg15Leu) rs545107676 0.00015
NM_000465.4(BARD1):c.1203T>C (p.Ser401=) rs370553043 0.00014
NM_000465.4(BARD1):c.279A>G (p.Gln93=) rs370000575 0.00014
NM_000465.4(BARD1):c.1152C>T (p.Ser384=) rs368291318 0.00012
NM_000465.4(BARD1):c.1059C>G (p.Pro353=) rs368649242 0.00009
NM_000465.4(BARD1):c.1694G>A (p.Arg565His) rs146946984 0.00009
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser) rs587781976 0.00008
NM_000465.4(BARD1):c.687T>C (p.Phe229=) rs756803590 0.00008
NM_000465.4(BARD1):c.1586G>A (p.Arg529Gln) rs753479021 0.00006
NM_000465.4(BARD1):c.1973G>A (p.Arg658His) rs377227840 0.00006
NM_000465.4(BARD1):c.1353A>T (p.Gly451=) rs369564500 0.00005
NM_000465.4(BARD1):c.1568T>C (p.Val523Ala) rs587780017 0.00005
NM_000465.4(BARD1):c.1593C>T (p.Val531=) rs564894014 0.00005
NM_000465.4(BARD1):c.738A>G (p.Pro246=) rs587780859 0.00005
NM_000465.4(BARD1):c.2280G>A (p.Ser760=) rs749959440 0.00004
NM_000465.4(BARD1):c.783A>G (p.Leu261=) rs201862973 0.00004
NM_000465.4(BARD1):c.564T>G (p.Pro188=) rs748511245 0.00002
NM_000465.4(BARD1):c.945A>T (p.Pro315=) rs876660284 0.00002
NM_000465.4(BARD1):c.1443C>T (p.Leu481=) rs1286691671 0.00001
NM_000465.4(BARD1):c.15G>C (p.Arg5=) rs769204862 0.00001
NM_000465.4(BARD1):c.1626A>G (p.Leu542=) rs786201551 0.00001
NM_000465.4(BARD1):c.1689G>A (p.Gly563=) rs762745326 0.00001
NM_000465.4(BARD1):c.1704A>G (p.Gly568=) rs1057520238 0.00001
NM_000465.4(BARD1):c.171G>C (p.Leu57=) rs876659045 0.00001
NM_000465.4(BARD1):c.1729C>T (p.Leu577=) rs749756887 0.00001
NM_000465.4(BARD1):c.1731G>A (p.Leu577=) rs863224364 0.00001
NM_000465.4(BARD1):c.2145G>A (p.Gln715=) rs760541330 0.00001
NM_000465.4(BARD1):c.2253G>T (p.Arg751=) rs750001065 0.00001
NM_000465.4(BARD1):c.300A>G (p.Gln100=) rs977731407 0.00001
NM_000465.4(BARD1):c.95G>T (p.Gly32Val) rs587782675 0.00001
NM_000465.4(BARD1):c.117C>T (p.Ala39=) rs786202271
NM_000465.4(BARD1):c.1311T>C (p.Ile437=) rs876659789
NM_000465.4(BARD1):c.1438T>C (p.Leu480=) rs786203220
NM_000465.4(BARD1):c.1461G>T (p.Val487=) rs1694272372
NM_000465.4(BARD1):c.1467C>T (p.Thr489=) rs1694271621
NM_000465.4(BARD1):c.1479A>G (p.Gln493=) rs375029767
NM_000465.4(BARD1):c.1518_1519delinsCT (p.Val507Leu) rs386654966
NM_000465.4(BARD1):c.1644G>A (p.Lys548=) rs1064796411
NM_000465.4(BARD1):c.165C>T (p.Asn55=) rs1553625775
NM_000465.4(BARD1):c.1692G>A (p.Gln564=) rs1168537193
NM_000465.4(BARD1):c.1986C>T (p.Leu662=) rs1553612477
NM_000465.4(BARD1):c.222T>C (p.Cys74=) rs1168791343
NM_000465.4(BARD1):c.615G>A (p.Lys205=) rs766609646
NM_000465.4(BARD1):c.897T>C (p.Thr299=) rs559051241
NM_000465.4(BARD1):c.924T>G (p.Leu308=) rs758559877
NM_000465.4(BARD1):c.946T>C (p.Leu316=) rs587782325

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.