ClinVar Miner

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

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Total variants: 39
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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.842C>T (p.Pro281Leu) rs367890377 0.00021
NM_000465.4(BARD1):c.1554C>T (p.Ala518=) rs139612775 0.00015
NM_000465.4(BARD1):c.1059C>G (p.Pro353=) rs368649242 0.00009
NM_000465.4(BARD1):c.687T>C (p.Phe229=) rs756803590 0.00008
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.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.1028C>T (p.Thr343Ile) rs201032007 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.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.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.2136C>T (p.Asp712=) rs759046999 0.00001
NM_000465.4(BARD1):c.2145G>A (p.Gln715=) rs760541330 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.765T>C (p.Asn255=) rs754775017 0.00001
NM_000465.4(BARD1):c.864T>C (p.Ser288=) rs771982631 0.00001
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.1866T>C (p.Leu622=) rs368195514
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.345A>G (p.Leu115=) rs771012953
NM_000465.4(BARD1):c.365-8del rs776103948
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.789T>C (p.Ser263=) rs1345594874

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