ClinVar Miner

List of variants in gene BARD1 reported as uncertain significance by Mendelics

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Total variants: 57
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HGVS dbSNP gnomAD frequency
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.842C>T (p.Pro281Leu) rs367890377 0.00021
NM_000465.4(BARD1):c.308G>A (p.Ser103Asn) rs145629242 0.00019
NM_000465.4(BARD1):c.1835A>T (p.Asp612Val) rs201140528 0.00011
NM_000465.4(BARD1):c.1339C>G (p.Leu447Val) rs376727038 0.00008
NM_000465.4(BARD1):c.716T>A (p.Leu239Gln) rs200359745 0.00006
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys) rs3738885 0.00006
NM_000465.4(BARD1):c.1268A>G (p.Lys423Arg) rs749383704 0.00005
NM_000465.4(BARD1):c.841C>T (p.Pro281Ser) rs200059956 0.00005
NM_000465.4(BARD1):c.160A>G (p.Thr54Ala) rs200254470 0.00004
NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr) rs587780030 0.00004
NM_000465.4(BARD1):c.353A>G (p.Asn118Ser) rs142864491 0.00004
NM_000465.4(BARD1):c.1028C>T (p.Thr343Ile) rs201032007 0.00003
NM_000465.4(BARD1):c.1247T>G (p.Leu416Arg) rs878853996 0.00003
NM_000465.4(BARD1):c.1915T>C (p.Cys639Arg) rs587781376 0.00003
NM_000465.4(BARD1):c.77T>G (p.Met26Arg) rs759957629 0.00003
NM_000465.4(BARD1):c.1569-13C>G rs587780018 0.00002
NM_000465.4(BARD1):c.1109G>A (p.Arg370His) rs730881416 0.00001
NM_000465.4(BARD1):c.1543T>C (p.Ser515Pro) rs876659146 0.00001
NM_000465.4(BARD1):c.1594G>A (p.Asp532Asn) rs757281184 0.00001
NM_000465.4(BARD1):c.1802A>G (p.Asp601Gly) rs767765131 0.00001
NM_000465.4(BARD1):c.2054A>G (p.His685Arg) rs368488821 0.00001
NM_000465.4(BARD1):c.2057A>G (p.His686Arg) rs864622380 0.00001
NM_000465.4(BARD1):c.2155A>G (p.Thr719Ala) rs771852699 0.00001
NM_000465.4(BARD1):c.490C>G (p.Gln164Glu) rs750350372 0.00001
NM_000465.4(BARD1):c.976A>G (p.Asn326Asp) rs587780038 0.00001
NM_000465.4(BARD1):c.986C>G (p.Ser329Cys) rs905626929 0.00001
NM_000465.4(BARD1):c.1002G>T (p.Lys334Asn) rs1574818027
NM_000465.4(BARD1):c.1045A>C (p.Lys349Gln) rs1401955290
NM_000465.4(BARD1):c.1136A>C (p.Lys379Thr) rs750827325
NM_000465.4(BARD1):c.1288A>G (p.Thr430Ala) rs1574815970
NM_000465.4(BARD1):c.1297C>T (p.His433Tyr) rs1574815914
NM_000465.4(BARD1):c.1314+5G>A rs868089048
NM_000465.4(BARD1):c.1335A>C (p.Glu445Asp) rs1574792945
NM_000465.4(BARD1):c.1376A>G (p.His459Arg) rs587781621
NM_000465.4(BARD1):c.1564G>T (p.Ala522Ser) rs730881419
NM_000465.4(BARD1):c.1610A>G (p.Glu537Gly) rs1553616390
NM_000465.4(BARD1):c.1754T>C (p.Leu585Pro) rs786201905
NM_000465.4(BARD1):c.1816C>T (p.His606Tyr) rs1559386300
NM_000465.4(BARD1):c.1886G>T (p.Trp629Leu) rs747446711
NM_000465.4(BARD1):c.1906G>A (p.Val636Ile) rs1553612541
NM_000465.4(BARD1):c.1955A>G (p.Glu652Gly) rs876658395
NM_000465.4(BARD1):c.2125C>T (p.Pro709Ser) rs1040231633
NM_000465.4(BARD1):c.2165A>G (p.Tyr722Cys) rs2105987106
NM_000465.4(BARD1):c.2192G>A (p.Arg731His) rs587782248
NM_000465.4(BARD1):c.2206T>C (p.Tyr736His) rs1559371905
NM_000465.4(BARD1):c.2216A>G (p.Tyr739Cys) rs777013688
NM_000465.4(BARD1):c.491A>C (p.Gln164Pro) rs980413835
NM_000465.4(BARD1):c.53A>T (p.Asn18Ile) rs1064793727
NM_000465.4(BARD1):c.565G>A (p.Ala189Thr) rs786202110
NM_000465.4(BARD1):c.675A>T (p.Glu225Asp) rs1559425348
NM_000465.4(BARD1):c.69_70insAACGAGCCTCGTTCCG (p.Pro24fs) rs2106171546
NM_000465.4(BARD1):c.752G>A (p.Ser251Asn) rs1553622477
NM_000465.4(BARD1):c.769G>A (p.Glu257Lys) rs587782673
NM_000465.4(BARD1):c.7G>T (p.Asp3Tyr) rs1060501282
NM_000465.4(BARD1):c.994A>T (p.Ile332Phe) rs543606863

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