ClinVar Miner

List of variants in gene BARD1 reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 50
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HGVS dbSNP gnomAD frequency
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.659T>C (p.Leu220Ser) rs138593305 0.00013
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.1586G>A (p.Arg529Gln) rs753479021 0.00006
NM_000465.4(BARD1):c.-4G>A rs761863671 0.00005
NM_000465.4(BARD1):c.2172G>T (p.Ala724=) rs143331809 0.00004
NM_000465.4(BARD1):c.353A>G (p.Asn118Ser) rs142864491 0.00004
NM_000465.4(BARD1):c.581G>A (p.Arg194Lys) rs181748854 0.00004
NM_000465.4(BARD1):c.1052C>T (p.Thr351Met) rs767208122 0.00003
NM_000465.4(BARD1):c.1148T>A (p.Met383Lys) rs763596413 0.00003
NM_000465.4(BARD1):c.2171C>T (p.Ala724Val) rs587782662 0.00003
NM_000465.4(BARD1):c.266C>T (p.Pro89Leu) rs780241203 0.00003
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn) rs369561166 0.00003
NM_000465.4(BARD1):c.2279C>T (p.Ser760Leu) rs730881425 0.00002
NM_000465.4(BARD1):c.556A>G (p.Ser186Gly) rs16852741 0.00002
NM_000465.4(BARD1):c.1448A>G (p.His483Arg) rs587781874 0.00001
NM_000465.4(BARD1):c.1868G>A (p.Gly623Glu) rs587782252 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.1963G>C (p.Glu655Gln) rs786203772 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.274A>T (p.Ile92Leu) rs750878896 0.00001
NM_000465.4(BARD1):c.300A>G (p.Gln100=) rs977731407 0.00001
NM_000465.4(BARD1):c.382C>T (p.Pro128Ser) rs878854011 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
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.1309A>G (p.Ile437Val) rs764592698
NM_000465.4(BARD1):c.175G>C (p.Glu59Gln) rs1559441880
NM_000465.4(BARD1):c.1904-12_1904-10delinsGGG rs2105990964
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.2148_2149del (p.Ile717fs) rs786203811
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly) rs76744638
NM_000465.4(BARD1):c.643A>T (p.Asn215Tyr) rs864622353
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.888A>C (p.Glu296Asp) rs2106109942
NM_000465.4(BARD1):c.895A>G (p.Thr299Ala) rs1694983227

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