ClinVar Miner

List of variants in gene BARD1 reported as likely benign for not provided

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Gene type:
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Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1568+111A>C rs5031005 0.02739
NM_000465.4(BARD1):c.158+188G>T rs71579843 0.02164
NM_000465.4(BARD1):c.215+59_215+60del rs67240037 0.01582
NM_000465.4(BARD1):c.216-62G>A rs140327786 0.01380
NM_000465.4(BARD1):c.159-261T>G rs75146556 0.01204
NM_000465.4(BARD1):c.1315-168C>T rs147670282 0.00876
NM_000465.4(BARD1):c.365-185G>A rs7563831 0.00870
NM_000465.4(BARD1):c.1678-60T>C rs4986842 0.00718
NM_000465.4(BARD1):c.1903+145G>A rs146298985 0.00676
NM_000465.4(BARD1):c.1315-285G>A rs116494562 0.00661
NM_000465.4(BARD1):c.159-42A>C rs148092589 0.00654
NM_000465.4(BARD1):c.1904-67A>G rs4986840 0.00623
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys) rs35306212 0.00455
NM_000465.4(BARD1):c.1677+206T>C rs115828789 0.00430
NM_000465.4(BARD1):c.1903+892C>A rs140879108 0.00378
NM_000465.4(BARD1):c.2001+224C>T rs113815630 0.00372
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.1569-184G>A rs80226752 0.00158
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn) rs142155101 0.00153
NM_000465.4(BARD1):c.158+41G>T rs555835196 0.00124
NM_000465.4(BARD1):c.216-13A>T rs1272210676 0.00086
NM_000465.4(BARD1):c.144G>A (p.Leu48=) rs151168457 0.00050
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.1347A>G (p.Gln449=) rs373257776 0.00021
NM_000465.4(BARD1):c.842C>T (p.Pro281Leu) rs367890377 0.00021
NM_000465.4(BARD1):c.57G>A (p.Glu19=) rs730881406 0.00019
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.1152C>T (p.Ser384=) rs368291318 0.00012
NM_000465.4(BARD1):c.1568+15G>T rs145936354 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.1409A>G (p.Asn470Ser) rs587781976 0.00008
NM_000465.4(BARD1):c.687T>C (p.Phe229=) rs756803590 0.00008
NM_000465.4(BARD1):c.1586G>A (p.Arg529Gln) rs753479021 0.00006
NM_000465.4(BARD1):c.1734T>A (p.Ser578=) rs373449212 0.00006
NM_000465.4(BARD1):c.1973G>A (p.Arg658His) rs377227840 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.2172G>T (p.Ala724=) rs143331809 0.00004
NM_000465.4(BARD1):c.2280G>A (p.Ser760=) rs749959440 0.00004
NM_000465.4(BARD1):c.365-7C>T rs745929983 0.00004
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr) rs146223579 0.00004
NM_000465.4(BARD1):c.1028C>T (p.Thr343Ile) rs201032007 0.00003
NM_000465.4(BARD1):c.1533G>A (p.Lys511=) rs371785856 0.00003
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn) rs369561166 0.00003
NM_000465.4(BARD1):c.1194A>G (p.Thr398=) rs781482219 0.00002
NM_000465.4(BARD1):c.159T>C (p.Cys53=) rs201708813 0.00002
NM_000465.4(BARD1):c.2083G>A (p.Val695Ile) rs111367604 0.00002
NM_000465.4(BARD1):c.267G>A (p.Pro89=) rs756165637 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.977A>G (p.Asn326Ser) rs779960429 0.00002
NM_000465.4(BARD1):c.1218A>T (p.Arg406=) rs757900534 0.00001
NM_000465.4(BARD1):c.1389A>G (p.Thr463=) rs748796794 0.00001
NM_000465.4(BARD1):c.1452G>A (p.Lys484=) rs201841770 0.00001
NM_000465.4(BARD1):c.1456T>C (p.Leu486=) rs1446646798 0.00001
NM_000465.4(BARD1):c.1470C>T (p.Thr490=) rs758895846 0.00001
NM_000465.4(BARD1):c.1497C>T (p.His499=) rs760665188 0.00001
NM_000465.4(BARD1):c.1629G>A (p.Leu543=) rs748646220 0.00001
NM_000465.4(BARD1):c.1695T>C (p.Arg565=) rs569636814 0.00001
NM_000465.4(BARD1):c.1704A>G (p.Gly568=) rs1057520238 0.00001
NM_000465.4(BARD1):c.1731G>A (p.Leu577=) rs863224364 0.00001
NM_000465.4(BARD1):c.1881A>C (p.Gly627=) rs968535447 0.00001
NM_000465.4(BARD1):c.1920A>G (p.Leu640=) rs780901872 0.00001
NM_000465.4(BARD1):c.2136C>T (p.Asp712=) rs759046999 0.00001
NM_000465.4(BARD1):c.2145G>A (p.Gln715=) rs760541330 0.00001
NM_000465.4(BARD1):c.2178C>T (p.Pro726=) rs201873551 0.00001
NM_000465.4(BARD1):c.2202A>G (p.Thr734=) rs786201370 0.00001
NM_000465.4(BARD1):c.2328C>T (p.Asp776=) rs863224673 0.00001
NM_000465.4(BARD1):c.468T>C (p.Tyr156=) rs1436038663 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.75C>T (p.Ala25=) rs763098407 0.00001
NM_000465.4(BARD1):c.765T>C (p.Asn255=) rs754775017 0.00001
NM_000465.4(BARD1):c.864T>C (p.Ser288=) rs771982631 0.00001
NM_000465.4(BARD1):c.*136_*138dup rs113789798
NM_000465.4(BARD1):c.*316T>C
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del) rs28997575
NM_000465.4(BARD1):c.117C>G (p.Ala39=) rs786202271
NM_000465.4(BARD1):c.117C>T (p.Ala39=) rs786202271
NM_000465.4(BARD1):c.1248G>A (p.Leu416=) rs1426931125
NM_000465.4(BARD1):c.1314+99_1314+106del rs141351703
NM_000465.4(BARD1):c.1396-279G>C rs71579849
NM_000465.4(BARD1):c.1479A>G (p.Gln493=) rs375029767
NM_000465.4(BARD1):c.1518_1519delinsCT (p.Val507Leu) rs386654966
NM_000465.4(BARD1):c.1650A>G (p.Glu550=) rs1559394684
NM_000465.4(BARD1):c.1866T>C (p.Leu622=) rs368195514
NM_000465.4(BARD1):c.1914A>G (p.Ala638=) rs876658489
NM_000465.4(BARD1):c.2002-114A>G rs147982569
NM_000465.4(BARD1):c.216-29dup rs56130510
NM_000465.4(BARD1):c.2160C>T (p.Val720=) rs137888190
NM_000465.4(BARD1):c.2163A>G (p.Ala721=) rs786202805
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.2191C>T (p.Arg731Cys) rs76744638
NM_000465.4(BARD1):c.297A>G (p.Arg99=) rs878854010
NM_000465.4(BARD1):c.365-8del rs776103948
NM_000465.4(BARD1):c.607G>A (p.Gly203Arg) rs730881415
NM_000465.4(BARD1):c.609A>G (p.Gly203=) rs28997574
NM_000465.4(BARD1):c.615G>A (p.Lys205=) rs766609646
NM_000465.4(BARD1):c.699G>A (p.Glu233=) rs1002531703
NM_000465.4(BARD1):c.702A>G (p.Glu234=) rs786202878
NM_000465.4(BARD1):c.789T>C (p.Ser263=) rs1345594874
NM_000465.4(BARD1):c.93C>G (p.Arg31=) rs778803692

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