List of variants in gene BARD1 reported as benign for not specified

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1518T>C (p.His506=)	rs2070093	0.74904
NM_000465.4(BARD1):c.1134G>C (p.Arg378Ser)	rs2229571	0.53291
NM_000465.4(BARD1):c.1315-19G>A	rs6704780	0.37148
NM_000465.4(BARD1):c.1568+14C>T	rs5031011	0.34966
NM_000465.4(BARD1):c.70C>T (p.Pro24Ser)	rs1048108	0.32854
NM_000465.4(BARD1):c.1053G>C (p.Thr351=)	rs2070096	0.19573
NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg)	rs2228456	0.02135
NM_000465.4(BARD1):c.1314+29C>G	rs71579845	0.01508
NM_000465.4(BARD1):c.1670G>C (p.Cys557Ser)	rs28997576	0.01443
NM_000465.4(BARD1):c.609A>C (p.Gly203=)	rs28997574	0.00787
NM_000465.4(BARD1):c.2212A>G (p.Ile738Val)	rs61754118	0.00745
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys)	rs3738888	0.00736
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.2282G>A (p.Ser761Asn)	rs142155101	0.00153
NM_000465.4(BARD1):c.90T>A (p.Gly30=)	rs150354152	0.00088
NM_000465.4(BARD1):c.1678-20A>G	rs189401077	0.00051
NM_000465.4(BARD1):c.215+12C>T	rs373816832	0.00049
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.346C>T (p.His116Tyr)	rs144856889	0.00029
NM_000465.4(BARD1):c.1491A>G (p.Pro497=)	rs61754117	0.00027
NM_000465.4(BARD1):c.1347A>G (p.Gln449=)	rs373257776	0.00021
NM_000465.4(BARD1):c.57G>A (p.Glu19=)	rs730881406	0.00019
NM_000465.4(BARD1):c.2082C>T (p.Leu694=)	rs139620052	0.00018
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.2002-11C>T	rs187240320	0.00010
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.722C>G (p.Ser241Cys)	rs3738885	0.00006
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.2280G>A (p.Ser760=)	rs749959440	0.00004
NM_000465.4(BARD1):c.253G>T (p.Val85Leu)	rs370359540	0.00004
NM_000465.4(BARD1):c.783A>G (p.Leu261=)	rs201862973	0.00004
NM_000465.4(BARD1):c.364+17T>C	rs375358131	0.00001
NM_000465.4(BARD1):c.882G>A (p.Arg294=)	rs778855056	0.00001
NM_000465.3(BARD1):c.1518_1519invTG (p.Val507Met)
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del)	rs28997575
NM_000465.4(BARD1):c.1519G>A (p.Val507Met)	rs2070094
NM_000465.4(BARD1):c.216-14del	rs56130510
NM_000465.4(BARD1):c.216-29dup	rs56130510
NM_000465.4(BARD1):c.216-9A>T	rs759575504
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638
NM_000465.4(BARD1):c.365-8del	rs776103948

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