List of variants in gene BARD1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 44

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HGVS	dbSNP	gnomAD frequency
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.90T>A (p.Gly30=)	rs150354152	0.00088
NM_000465.4(BARD1):c.1515G>T (p.Gly505=)	rs139721211	0.00029
NM_000465.4(BARD1):c.1491A>G (p.Pro497=)	rs61754117	0.00027
NM_000465.4(BARD1):c.2082C>T (p.Leu694=)	rs139620052	0.00018
NM_000465.4(BARD1):c.1554C>T (p.Ala518=)	rs139612775	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.1568+15G>T	rs145936354	0.00010
NM_000465.4(BARD1):c.1694G>A (p.Arg565His)	rs146946984	0.00009
NM_000465.4(BARD1):c.687T>C (p.Phe229=)	rs756803590	0.00008
NM_000465.4(BARD1):c.1734T>A (p.Ser578=)	rs373449212	0.00006
NM_000465.4(BARD1):c.-4G>A	rs761863671	0.00005
NM_000465.4(BARD1):c.738A>G (p.Pro246=)	rs587780859	0.00005
NM_000465.4(BARD1):c.1473G>A (p.Gly491=)	rs151080730	0.00004
NM_000465.4(BARD1):c.1788A>G (p.Lys596=)	rs777084777	0.00004
NM_000465.4(BARD1):c.1533G>A (p.Lys511=)	rs371785856	0.00003
NM_000465.4(BARD1):c.48C>T (p.Ser16=)	rs770753803	0.00003
NM_000465.4(BARD1):c.159-7C>T	rs533403598	0.00002
NM_000465.4(BARD1):c.159T>C (p.Cys53=)	rs201708813	0.00002
NM_000465.4(BARD1):c.531A>G (p.Gln177=)	rs774050888	0.00002
NM_000465.4(BARD1):c.564T>G (p.Pro188=)	rs748511245	0.00002
NM_000465.4(BARD1):c.1218A>T (p.Arg406=)	rs757900534	0.00001
NM_000465.4(BARD1):c.1383A>G (p.Gly461=)	rs148821907	0.00001
NM_000465.4(BARD1):c.1614T>C (p.Ser538=)	rs781448650	0.00001
NM_000465.4(BARD1):c.1818T>C (p.His606=)	rs199590147	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.651A>G (p.Lys217=)	rs768866006	0.00001
NM_000465.4(BARD1):c.669A>G (p.Glu223=)	rs786201963	0.00001
NM_000465.4(BARD1):c.1053G>T (p.Thr351=)	rs2070096
NM_000465.4(BARD1):c.1062A>G (p.Ser354=)	rs1057521964
NM_000465.4(BARD1):c.1479A>G (p.Gln493=)	rs375029767
NM_000465.4(BARD1):c.1635A>G (p.Leu545=)	rs786203364
NM_000465.4(BARD1):c.1650A>G (p.Glu550=)	rs1559394684
NM_000465.4(BARD1):c.1904-5G>T	rs376639978
NM_000465.4(BARD1):c.2091A>T (p.Ala697=)	rs786201573
NM_000465.4(BARD1):c.2160C>T (p.Val720=)	rs137888190
NM_000465.4(BARD1):c.2169T>C (p.His723=)	rs779808630
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638
NM_000465.4(BARD1):c.357G>A (p.Glu119=)	rs1553624706
NM_000465.4(BARD1):c.93C>G (p.Arg31=)	rs778803692

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