ClinVar Miner

Variants in gene BARD1 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
934 626 0 65 73 2 7 127

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign association drug response risk factor
pathogenic 0 16 4 1 1 1 1 0
likely pathogenic 16 0 5 1 1 1 1 0
uncertain significance 4 5 0 72 17 1 1 0
likely benign 0 0 71 0 49 0 0 1
benign 0 0 16 49 0 0 0 1
risk factor 0 0 0 1 1 0 0 0

All variants with conflicting interpretations #

Total variants: 127
Download table as spreadsheet
HGVS dbSNP
NM_000465.3(BARD1):c.1518_1519invTG (p.Val507Met)
NM_000465.4(BARD1):c.*135_*138dup rs113789798
NM_000465.4(BARD1):c.-4G>A rs761863671
NM_000465.4(BARD1):c.1028C>T (p.Thr343Ile) rs201032007
NM_000465.4(BARD1):c.102G>A (p.Trp34Ter) rs879254280
NM_000465.4(BARD1):c.1053G>A (p.Thr351=) rs2070096
NM_000465.4(BARD1):c.1053G>C (p.Thr351=) rs2070096
NM_000465.4(BARD1):c.1053G>T (p.Thr351=) rs2070096
NM_000465.4(BARD1):c.1059C>G (p.Pro353=) rs368649242
NM_000465.4(BARD1):c.1070T>C (p.Ile357Thr) rs587781555
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del) rs28997575
NM_000465.4(BARD1):c.1127C>T (p.Ser376Leu) rs587782333
NM_000465.4(BARD1):c.1134G>C (p.Arg378Ser) rs2229571
NM_000465.4(BARD1):c.1147A>T (p.Met383Leu) rs761516178
NM_000465.4(BARD1):c.1194A>G (p.Thr398=) rs781482219
NM_000465.4(BARD1):c.1196T>G (p.Leu399Ter)
NM_000465.4(BARD1):c.1203T>C (p.Ser401=) rs370553043
NM_000465.4(BARD1):c.1205C>A (p.Ser402Ter) rs796666047
NM_000465.4(BARD1):c.1216C>T (p.Arg406Ter) rs377153250
NM_000465.4(BARD1):c.1224_1227del (p.Met408fs) rs1553622164
NM_000465.4(BARD1):c.1317C>T (p.Gly439=) rs369986649
NM_000465.4(BARD1):c.1325del (p.Pro442fs) rs1060501287
NM_000465.4(BARD1):c.1347A>G (p.Gln449=) rs373257776
NM_000465.4(BARD1):c.1393T>C (p.Leu465=) rs779653364
NM_000465.4(BARD1):c.1395+4G>T rs1025329798
NM_000465.4(BARD1):c.1396-22_1396-19del rs765080315
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser) rs587781976
NM_000465.4(BARD1):c.1448A>G (p.His483Arg) rs587781874
NM_000465.4(BARD1):c.144G>A (p.Leu48=) rs151168457
NM_000465.4(BARD1):c.1473G>A (p.Gly491=) rs151080730
NM_000465.4(BARD1):c.1479A>G (p.Gln493=) rs375029767
NM_000465.4(BARD1):c.1491A>G (p.Pro497=) rs61754117
NM_000465.4(BARD1):c.1515G>T (p.Gly505=) rs139721211
NM_000465.4(BARD1):c.1518T>C (p.His506=) rs2070093
NM_000465.4(BARD1):c.1518_1519delinsCT (p.Val507Leu) rs386654966
NM_000465.4(BARD1):c.1519G>A (p.Val507Met) rs2070094
NM_000465.4(BARD1):c.1568+14C>T rs5031011
NM_000465.4(BARD1):c.1568T>C (p.Val523Ala) rs587780017
NM_000465.4(BARD1):c.1569-9T>C rs753153934
NM_000465.4(BARD1):c.1586G>A (p.Arg529Gln) rs753479021
NM_000465.4(BARD1):c.160A>G (p.Thr54Ala) rs200254470
NM_000465.4(BARD1):c.1613G>A (p.Ser538Asn) rs370771157
NM_000465.4(BARD1):c.1644G>A (p.Lys548=) rs1064796411
NM_000465.4(BARD1):c.1652C>G (p.Ser551Ter) rs587781707
NM_000465.4(BARD1):c.1670G>C (p.Cys557Ser) rs28997576
NM_000465.4(BARD1):c.1678-20A>G rs189401077
NM_000465.4(BARD1):c.1694G>A (p.Arg565His) rs146946984
NM_000465.4(BARD1):c.172_173AG[2] (p.Glu59fs) rs1057517589
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys) rs35306212
NM_000465.4(BARD1):c.1835A>T (p.Asp612Val) rs201140528
NM_000465.4(BARD1):c.1877A>G (p.Asn626Ser) rs587781443
NM_000465.4(BARD1):c.1904-17T>A rs1064795448
NM_000465.4(BARD1):c.1904-5G>A rs376639978
NM_000465.4(BARD1):c.1904-5G>T rs376639978
NM_000465.4(BARD1):c.1922G>A (p.Arg641Gln) rs752870879
NM_000465.4(BARD1):c.1932_1933del (p.Val644_Cys645insTer) rs587782504
NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg) rs2228456
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs) rs587780024
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys) rs3738888
NM_000465.4(BARD1):c.1973G>A (p.Arg658His) rs377227840
NM_000465.4(BARD1):c.1977A>G (p.Arg659=) rs147215925
NM_000465.4(BARD1):c.1996C>T (p.Gln666Ter) rs730881422
NM_000465.4(BARD1):c.2002-11C>T rs187240320
NM_000465.4(BARD1):c.2002-12T>G rs587780027
NM_000465.4(BARD1):c.2002-1G>A rs762601855
NM_000465.4(BARD1):c.2002-2A>C rs876658260
NM_000465.4(BARD1):c.2002-2A>T rs876658260
NM_000465.4(BARD1):c.2063dup (p.Asp689fs) rs1064796026
NM_000465.4(BARD1):c.2075T>C (p.Ile692Thr) rs587782555
NM_000465.4(BARD1):c.2082C>T (p.Leu694=) rs139620052
NM_000465.4(BARD1):c.2083G>A (p.Val695Ile) rs111367604
NM_000465.4(BARD1):c.2116A>G (p.Lys706Glu) rs149262370
NM_000465.4(BARD1):c.2148_2149del (p.Ile717fs) rs786203811
NM_000465.4(BARD1):c.215+12C>T rs373816832
NM_000465.4(BARD1):c.215+13G>A rs886055601
NM_000465.4(BARD1):c.216-14T>C rs775103922
NM_000465.4(BARD1):c.216-14del rs56130510
NM_000465.4(BARD1):c.216-15_216-14del rs56130510
NM_000465.4(BARD1):c.2179G>A (p.Asp727Asn) rs730881424
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly) rs76744638
NM_000465.4(BARD1):c.2212A>G (p.Ile738Val) rs61754118
NM_000465.4(BARD1):c.2280G>A (p.Ser760=) rs749959440
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn) rs142155101
NM_000465.4(BARD1):c.2296_2297TG[2] (p.Val767fs) rs750413473
NM_000465.4(BARD1):c.252A>G (p.Pro84=) rs786202670
NM_000465.4(BARD1):c.253G>T (p.Val85Leu) rs370359540
NM_000465.4(BARD1):c.267G>A (p.Pro89=) rs756165637
NM_000465.4(BARD1):c.279A>G (p.Gln93=) rs370000575
NM_000465.4(BARD1):c.335G>A (p.Arg112Gln) rs587781591
NM_000465.4(BARD1):c.33G>T (p.Gln11His) rs143914387
NM_000465.4(BARD1):c.346C>T (p.His116Tyr) rs144856889
NM_000465.4(BARD1):c.348T>C (p.His116=) rs139934362
NM_000465.4(BARD1):c.353A>G (p.Asn118Ser) rs142864491
NM_000465.4(BARD1):c.364+17T>C rs375358131
NM_000465.4(BARD1):c.364+7A>C rs1475396127
NM_000465.4(BARD1):c.365-14_365-13dup rs776103948
NM_000465.4(BARD1):c.365-8del rs776103948
NM_000465.4(BARD1):c.382C>T (p.Pro128Ser) rs878854011
NM_000465.4(BARD1):c.44G>T (p.Arg15Leu) rs545107676
NM_000465.4(BARD1):c.465A>G (p.Arg155=) rs730881413
NM_000465.4(BARD1):c.469G>A (p.Val157Ile) rs1553622662
NM_000465.4(BARD1):c.521G>A (p.Ser174Asn) rs1277839212
NM_000465.4(BARD1):c.55G>T (p.Glu19Ter) rs752514155
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn) rs369561166
NM_000465.4(BARD1):c.57G>A (p.Glu19=) rs730881406
NM_000465.4(BARD1):c.581G>A (p.Arg194Lys) rs181748854
NM_000465.4(BARD1):c.607G>A (p.Gly203Arg) rs730881415
NM_000465.4(BARD1):c.609A>C (p.Gly203=) rs28997574
NM_000465.4(BARD1):c.620A>G (p.Lys207Arg) rs34969857
NM_000465.4(BARD1):c.627_628del (p.Lys209fs) rs864622223
NM_000465.4(BARD1):c.659T>C (p.Leu220Ser) rs138593305
NM_000465.4(BARD1):c.668A>G (p.Glu223Gly) rs145009419
NM_000465.4(BARD1):c.684A>G (p.Glu228=) rs780627045
NM_000465.4(BARD1):c.709C>G (p.Gln237Glu) rs587780035
NM_000465.4(BARD1):c.70C>T (p.Pro24Ser) rs1048108
NM_000465.4(BARD1):c.716T>A (p.Leu239Gln) rs200359745
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys) rs3738885
NM_000465.4(BARD1):c.738A>G (p.Pro246=) rs587780859
NM_000465.4(BARD1):c.73G>C (p.Ala25Pro) rs751646468
NM_000465.4(BARD1):c.748T>G (p.Ser250Ala) rs570022823
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr) rs146223579
NM_000465.4(BARD1):c.783A>G (p.Leu261=) rs201862973
NM_000465.4(BARD1):c.79G>C (p.Glu27Gln) rs587780037
NM_000465.4(BARD1):c.79G>T (p.Glu27Ter) rs587780037
NM_000465.4(BARD1):c.90T>A (p.Gly30=) rs150354152
NM_000465.4(BARD1):c.977A>G (p.Asn326Ser) rs779960429
Single allele

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