List of variants in gene BARD1 reported as benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg)	rs2228456	0.02135
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.33G>T (p.Gln11His)	rs143914387	0.00176
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.144G>A (p.Leu48=)	rs151168457	0.00050
NM_000465.4(BARD1):c.348T>C (p.His116=)	rs139934362	0.00039
NM_000465.4(BARD1):c.1491A>G (p.Pro497=)	rs61754117	0.00027
NM_000465.4(BARD1):c.308G>A (p.Ser103Asn)	rs145629242	0.00019
NM_000465.4(BARD1):c.1203T>C (p.Ser401=)	rs370553043	0.00014
NM_000465.4(BARD1):c.1152C>T (p.Ser384=)	rs368291318	0.00012
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.1788A>G (p.Lys596=)	rs777084777	0.00004
NM_000465.4(BARD1):c.253G>T (p.Val85Leu)	rs370359540	0.00004
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr)	rs146223579	0.00004
NM_000465.4(BARD1):c.783A>G (p.Leu261=)	rs201862973	0.00004
NM_000465.4(BARD1):c.48C>T (p.Ser16=)	rs770753803	0.00003
NM_000465.4(BARD1):c.1695T>C (p.Arg565=)	rs569636814	0.00001
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del)	rs28997575
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638

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