ClinVar Miner

List of variants in gene BARD1 studied for Malignant tumor of breast

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Total variants: 73
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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.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.1515G>T (p.Gly505=) rs139721211 0.00029
NM_000465.4(BARD1):c.346C>T (p.His116Tyr) rs144856889 0.00029
NM_000465.4(BARD1):c.668A>G (p.Glu223Gly) rs145009419 0.00024
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.659T>C (p.Leu220Ser) rs138593305 0.00013
NM_000465.4(BARD1):c.1568+15G>T rs145936354 0.00010
NM_000465.4(BARD1):c.2002-11C>T rs187240320 0.00010
NM_000465.4(BARD1):c.1694G>A (p.Arg565His) rs146946984 0.00009
NM_000465.4(BARD1):c.2116A>G (p.Lys706Glu) rs149262370 0.00009
NM_000465.4(BARD1):c.764A>G (p.Asn255Ser) rs138904906 0.00009
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys) rs3738885 0.00006
NM_000465.4(BARD1):c.1921C>T (p.Arg641Ter) rs587781948 0.00004
NM_000465.4(BARD1):c.2172G>T (p.Ala724=) rs143331809 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.353A>G (p.Asn118Ser) rs142864491 0.00004
NM_000465.4(BARD1):c.365-7C>T rs745929983 0.00004
NM_000465.4(BARD1):c.1052C>T (p.Thr351Met) rs767208122 0.00003
NM_000465.4(BARD1):c.2242G>T (p.Glu748Ter) rs879253880 0.00003
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn) rs369561166 0.00003
NM_000465.4(BARD1):c.556A>G (p.Ser186Gly) rs16852741 0.00002
NM_000465.4(BARD1):c.1497C>T (p.His499=) rs760665188 0.00001
NM_000465.4(BARD1):c.1883G>T (p.Cys628Phe) rs1227794803 0.00001
NM_000465.4(BARD1):c.1904-10T>G rs768259863 0.00001
NM_000465.4(BARD1):c.1904-12T>G rs774178253 0.00001
NM_000465.4(BARD1):c.2155A>G (p.Thr719Ala) rs771852699 0.00001
NM_000465.4(BARD1):c.2253G>T (p.Arg751=) rs750001065 0.00001
NM_000465.4(BARD1):c.2294A>G (p.Asp765Gly) rs730881426 0.00001
NM_000465.4(BARD1):c.300A>G (p.Gln100=) rs977731407 0.00001
NM_000465.4(BARD1):c.334C>T (p.Arg112Ter) rs758972589 0.00001
NM_000465.4(BARD1):c.448C>T (p.Arg150Ter) rs730881411 0.00001
NM_000465.4(BARD1):c.632T>C (p.Leu211Ser) rs762171436 0.00001
NM_000465.4(BARD1):c.73G>C (p.Ala25Pro) rs751646468 0.00001
NM_000465.4(BARD1):c.835T>C (p.Ser279Pro) rs587781456 0.00001
NM_000465.4(BARD1):c.986C>G (p.Ser329Cys) rs905626929 0.00001
NC_000002.11:g.(?_215590369)_(215617280_215632205)del
NM_000465.4(BARD1):c.1060T>A (p.Ser354Thr) rs863224670
NM_000465.4(BARD1):c.1098_1099delinsAC (p.Ser367Pro) rs1064794052
NM_000465.4(BARD1):c.111T>A (p.Ser37Arg) rs2106171106
NM_000465.4(BARD1):c.130C>T (p.Leu44=) rs876658807
NM_000465.4(BARD1):c.1569-1_1677+2del rs2106038518
NM_000465.4(BARD1):c.1635A>G (p.Leu545=) rs786203364
NM_000465.4(BARD1):c.175G>C (p.Glu59Gln) rs1559441880
NM_000465.4(BARD1):c.176_177del (p.Glu59fs) rs1057517589
NM_000465.4(BARD1):c.1872del (p.Leu625fs) rs876659572
NM_000465.4(BARD1):c.1904-12_1904-10delinsGGG rs2105990964
NM_000465.4(BARD1):c.1904-502_*2del
NM_000465.4(BARD1):c.1932_1933del (p.Val644_Cys645insTer) rs587782504
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs) rs587780024
NM_000465.4(BARD1):c.1966G>C (p.Gly656Arg) rs766781362
NM_000465.4(BARD1):c.2001+3A>G rs1553612461
NM_000465.4(BARD1):c.2091A>T (p.Ala697=) rs786201573
NM_000465.4(BARD1):c.216-14del rs56130510
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly) rs76744638
NM_000465.4(BARD1):c.3G>A (p.Met1Ile) rs587780031
NM_000465.4(BARD1):c.623del (p.Lys208fs)
NM_000465.4(BARD1):c.627_628del (p.Lys209fs) rs864622223
NM_000465.4(BARD1):c.643A>T (p.Asn215Tyr) rs864622353
NM_000465.4(BARD1):c.673G>T (p.Glu225Ter) rs1064793049
NM_000465.4(BARD1):c.7G>A (p.Asp3Asn) rs1060501282
NM_000465.4(BARD1):c.833T>G (p.Val278Gly) rs1440649518
NM_000465.4(BARD1):c.895A>G (p.Thr299Ala) rs1694983227
NM_000465.4(BARD1):c.998_999del (p.Ile332_Ser333insTer) rs1482641121

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