ClinVar Miner

List of variants in gene BARD1 reported as likely pathogenic for carcinoma

Included ClinVar conditions (243):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 183
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HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1247T>G (p.Leu416Arg) rs878853996 0.00003
NM_000465.4(BARD1):c.2242G>T (p.Glu748Ter) rs879253880 0.00003
NM_000465.4(BARD1):c.1569-13C>G rs587780018 0.00002
NM_000465.4(BARD1):c.1205C>A (p.Ser402Ter) rs796666047 0.00001
NM_000465.4(BARD1):c.1678-1G>T rs767208318 0.00001
NC_000002.11:g.(?_215557064)_(215646033_?)del
NC_000002.11:g.(?_215593400)_(215595242_?)del
NC_000002.11:g.(?_215595125)_(215595242_?)del
NC_000002.11:g.(?_215609781)_(215617289_?)dup
NC_000002.11:g.(?_215609781)_(215661851_?)dup
NC_000002.11:g.(?_215632196)_(215657179_?)del
NC_000002.11:g.(?_215635923)_(215645654_?)del
NC_000002.11:g.(?_215645274)_(215657179_?)dup
NC_000002.11:g.(?_215657001)_(215661861_?)dup
NC_000002.11:g.(?_215657011)_(215661851_?)dup
NC_000002.12:g.(?_214728666)_(214730518_?)del
NC_000002.12:g.(?_214730216)_(214769312_?)del
NC_000002.12:g.(?_214767472)_(214767664_?)dup
NC_000002.12:g.(?_214767472)_(214781519_?)dup
NM_000465.4(BARD1):c.1000_1001insC (p.Lys334fs)
NM_000465.4(BARD1):c.1003del (p.Arg335fs)
NM_000465.4(BARD1):c.1061C>G (p.Ser354Ter) rs786202559
NM_000465.4(BARD1):c.1069dup (p.Ile357fs) rs2106108903
NM_000465.4(BARD1):c.1128del (p.Arg378fs)
NM_000465.4(BARD1):c.1146del (p.Asn382fs)
NM_000465.4(BARD1):c.1227_1231del (p.Ser410fs) rs1553622160
NM_000465.4(BARD1):c.1240del (p.Ala413_Met414insTer) rs1553622145
NM_000465.4(BARD1):c.1267A>T (p.Lys423Ter)
NM_000465.4(BARD1):c.1306_1314+7del rs1694934695
NM_000465.4(BARD1):c.1307_1314+11del
NM_000465.4(BARD1):c.1314+1G>A rs753785671
NM_000465.4(BARD1):c.133G>T (p.Glu45Ter)
NM_000465.4(BARD1):c.1345del (p.Gln449fs) rs2106081379
NM_000465.4(BARD1):c.1348_1349delinsCAT (p.Asn450fs) rs1553619713
NM_000465.4(BARD1):c.1349dup (p.Asn450fs) rs876660390
NM_000465.4(BARD1):c.1396-13A>G
NM_000465.4(BARD1):c.1396-1G>A rs2106077292
NM_000465.4(BARD1):c.1396-1G>C
NM_000465.4(BARD1):c.1396-1G>T
NM_000465.4(BARD1):c.1396-2A>C
NM_000465.4(BARD1):c.1407C>A (p.Cys469Ter) rs1553619349
NM_000465.4(BARD1):c.1543del (p.Ser515fs)
NM_000465.4(BARD1):c.1565_1568+298del rs2106075317
NM_000465.4(BARD1):c.1568+1G>A rs2106076135
NM_000465.4(BARD1):c.1568+1G>T
NM_000465.4(BARD1):c.1568+2T>C rs1553619196
NM_000465.4(BARD1):c.1568+5G>A
NM_000465.4(BARD1):c.1569-1G>A rs1574756672
NM_000465.4(BARD1):c.1569-1G>C rs1574756672
NM_000465.4(BARD1):c.1569-2A>C rs1693509336
NM_000465.4(BARD1):c.1569-2A>G rs1693509336
NM_000465.4(BARD1):c.1569-7T>G rs1559395026
NM_000465.4(BARD1):c.158+1G>A
NM_000465.4(BARD1):c.158+1G>T rs1553628351
NM_000465.4(BARD1):c.158+1_158+3delinsTT
NM_000465.4(BARD1):c.158+2_158+10del
NM_000465.4(BARD1):c.159-1G>A rs879254139
NM_000465.4(BARD1):c.159-1G>T rs879254139
NM_000465.4(BARD1):c.159-2A>C rs1424761304
NM_000465.4(BARD1):c.159T>G (p.Cys53Trp) rs201708813
NM_000465.4(BARD1):c.1658C>G (p.Ser553Ter)
NM_000465.4(BARD1):c.1662_1665del (p.Ser555fs) rs753537518
NM_000465.4(BARD1):c.1676_1677+23del rs1553616339
NM_000465.4(BARD1):c.1677+1G>A
NM_000465.4(BARD1):c.1677+1G>C rs1060501310
NM_000465.4(BARD1):c.1677+1G>T
NM_000465.4(BARD1):c.1677+2T>A
NM_000465.4(BARD1):c.1677+2T>C
NM_000465.4(BARD1):c.1677+5G>A rs587780019
NM_000465.4(BARD1):c.1678-1_1678del rs1553615184
NM_000465.4(BARD1):c.1678-1_1684del
NM_000465.4(BARD1):c.1678-2A>G rs1693089850
NM_000465.4(BARD1):c.1678-2A>T
NM_000465.4(BARD1):c.1678-3C>G rs1693089932
NM_000465.4(BARD1):c.1735dup (p.Ser579fs)
NM_000465.4(BARD1):c.1758del (p.Ser586fs) rs1559387024
NM_000465.4(BARD1):c.176_177del (p.Glu59fs) rs1057517589
NM_000465.4(BARD1):c.1788del (p.Lys596fs) rs1574739005
NM_000465.4(BARD1):c.1810+1G>A rs876659894
NM_000465.4(BARD1):c.1810+1_1810+32del
NM_000465.4(BARD1):c.1810+2T>G rs1234033325
NM_000465.4(BARD1):c.1810+3G>T rs1310430913
NM_000465.4(BARD1):c.1811-10_1811-2del rs879254264
NM_000465.4(BARD1):c.1811-1G>A rs879253952
NM_000465.4(BARD1):c.1811-1G>C rs879253952
NM_000465.4(BARD1):c.1811-2A>G rs1693044156
NM_000465.4(BARD1):c.1838_1841dup (p.Gln615fs)
NM_000465.4(BARD1):c.1865_1903+274del rs1693019491
NM_000465.4(BARD1):c.1872del (p.Leu625fs) rs876659572
NM_000465.4(BARD1):c.1903+1G>A rs876660237
NM_000465.4(BARD1):c.1903+1G>C
NM_000465.4(BARD1):c.1903+1G>T rs876660237
NM_000465.4(BARD1):c.1903+1del
NM_000465.4(BARD1):c.1903+2T>C rs1574737047
NM_000465.4(BARD1):c.1904-1G>A
NM_000465.4(BARD1):c.1904-1G>T
NM_000465.4(BARD1):c.1904-2A>T rs864622239
NM_000465.4(BARD1):c.1904-2del rs876659560
NM_000465.4(BARD1):c.1914_2001+77del
NM_000465.4(BARD1):c.1935_1954del (p.Cys645_Glu652delinsTer) rs587780024
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs) rs587780024
NM_000465.4(BARD1):c.1939C>T (p.Gln647Ter) rs1350570988
NM_000465.4(BARD1):c.1970del (p.Pro657fs) rs786203739
NM_000465.4(BARD1):c.1996C>T (p.Gln666Ter) rs730881422
NM_000465.4(BARD1):c.2001+1G>A rs768490891
NM_000465.4(BARD1):c.2001+1G>C rs768490891
NM_000465.4(BARD1):c.2001+3A>G rs1553612461
NM_000465.4(BARD1):c.2002-1G>A rs762601855
NM_000465.4(BARD1):c.2002-1G>C rs762601855
NM_000465.4(BARD1):c.2002-1G>T
NM_000465.4(BARD1):c.2002-2A>C rs876658260
NM_000465.4(BARD1):c.2002-2A>G rs876658260
NM_000465.4(BARD1):c.2002-2A>T rs876658260
NM_000465.4(BARD1):c.2003T>A (p.Leu668Ter) rs2105988065
NM_000465.4(BARD1):c.2020G>T (p.Gly674Ter) rs1328046615
NM_000465.4(BARD1):c.2024del (p.Cys675fs) rs2105987971
NM_000465.4(BARD1):c.2036T>A (p.Leu679Ter) rs1692227690
NM_000465.4(BARD1):c.2038_2042del (p.Trp680fs) rs1553612222
NM_000465.4(BARD1):c.2050A>T (p.Lys684Ter) rs1559372578
NM_000465.4(BARD1):c.2058_2061del (p.His686fs) rs2105987749
NM_000465.4(BARD1):c.2063dup (p.Asp689fs) rs1064796026
NM_000465.4(BARD1):c.2078dup (p.Leu694fs) rs1553612205
NM_000465.4(BARD1):c.2098_2099dup (p.Gln701fs)
NM_000465.4(BARD1):c.2099del (p.Gly700fs) rs1553612184
NM_000465.4(BARD1):c.2099dup (p.Gln701fs)
NM_000465.4(BARD1):c.2101C>T (p.Gln701Ter) rs587782348
NM_000465.4(BARD1):c.2109del (p.Ser704fs) rs2105987421
NM_000465.4(BARD1):c.2122_2124delinsCC (p.Lys708fs) rs1692217798
NM_000465.4(BARD1):c.2129_2132del (p.Asp710fs) rs1692216921
NM_000465.4(BARD1):c.212G>A (p.Cys71Tyr) rs1064793959
NM_000465.4(BARD1):c.2143C>T (p.Gln715Ter) rs1553612164
NM_000465.4(BARD1):c.2144dup (p.Thr716fs) rs1574703115
NM_000465.4(BARD1):c.2148_2149del (p.Ile717fs) rs786203811
NM_000465.4(BARD1):c.215+1G>A rs2106145519
NM_000465.4(BARD1):c.215+2T>A
NM_000465.4(BARD1):c.215+2T>C rs1559441760
NM_000465.4(BARD1):c.2157_2166del (p.Val720fs)
NM_000465.4(BARD1):c.216-1G>A rs876658905
NM_000465.4(BARD1):c.216-1G>C
NM_000465.4(BARD1):c.216-2A>G rs2106135562
NM_000465.4(BARD1):c.2166C>A (p.Tyr722Ter) rs2105987094
NM_000465.4(BARD1):c.2166C>G (p.Tyr722Ter)
NM_000465.4(BARD1):c.217_220del (p.Asn73fs)
NM_000465.4(BARD1):c.2203C>T (p.Gln735Ter)
NM_000465.4(BARD1):c.2208T>A (p.Tyr736Ter) rs2105986813
NM_000465.4(BARD1):c.2215dup (p.Tyr739fs)
NM_000465.4(BARD1):c.2218G>T (p.Glu740Ter) rs1692204026
NM_000465.4(BARD1):c.2229dup (p.Asn744Ter) rs1259296823
NM_000465.4(BARD1):c.2235T>A (p.Tyr745Ter)
NM_000465.4(BARD1):c.2235del (p.His746fs) rs2105986664
NM_000465.4(BARD1):c.2261_2262del (p.Lys754fs) rs1574702099
NM_000465.4(BARD1):c.2268G>A (p.Trp756Ter) rs786202118
NM_000465.4(BARD1):c.2279C>A (p.Ser760Ter) rs730881425
NM_000465.4(BARD1):c.2286G>A (p.Trp762Ter)
NM_000465.4(BARD1):c.2291_2294del (p.Ile764fs)
NM_000465.4(BARD1):c.2300_2301del (p.Val767fs) rs750413473
NM_000465.4(BARD1):c.272G>A (p.Trp91Ter) rs1559437094
NM_000465.4(BARD1):c.328A>T (p.Lys110Ter) rs1574839460
NM_000465.4(BARD1):c.362C>G (p.Ser121Ter)
NM_000465.4(BARD1):c.363_364+1del rs2106134415
NM_000465.4(BARD1):c.364+1G>A rs2106134408
NM_000465.4(BARD1):c.364+1G>T rs2106134408
NM_000465.4(BARD1):c.364+2T>G
NM_000465.4(BARD1):c.365-1G>T rs1559426428
NM_000465.4(BARD1):c.365-24_371del rs2106112761
NM_000465.4(BARD1):c.365-2A>T
NM_000465.4(BARD1):c.365-3315_793del
NM_000465.4(BARD1):c.46_68dup (p.Ala25fs) rs1553628445
NM_000465.4(BARD1):c.493del (p.Thr165fs)
NM_000465.4(BARD1):c.55G>T (p.Glu19Ter) rs752514155
NM_000465.4(BARD1):c.580_581del (p.Arg194fs)
NM_000465.4(BARD1):c.606del (p.Gly203fs)
NM_000465.4(BARD1):c.632T>G (p.Leu211Ter) rs762171436
NM_000465.4(BARD1):c.653G>A (p.Trp218Ter) rs1553622534
NM_000465.4(BARD1):c.672del (p.Glu225fs)
NM_000465.4(BARD1):c.716del (p.Leu239fs) rs2106110871
NM_000465.4(BARD1):c.838_839del (p.Leu280fs) rs876659752
NM_000465.4(BARD1):c.839dup (p.Leu280fs)
NM_000465.4(BARD1):c.860_861del (p.Glu287fs) rs786201868
NM_000465.4(BARD1):c.862_863insGG (p.Ser288fs)
NM_000465.4(BARD1):c.872del (p.Thr291fs) rs1574818832
NM_000465.4(BARD1):c.873dup (p.Lys292Ter) rs1553622378
Single allele

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