ClinVar Miner

List of variants reported as uncertain significance for BAP1-related tumor predisposition syndrome by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 223
Download table as spreadsheet
HGVS dbSNP
NC_000003.11:g.(?_52436298)_(52443900_?)dup
NM_004656.4(BAP1):c.1007T>C (p.Val336Ala)
NM_004656.4(BAP1):c.1020C>T (p.Gly340=) rs1553645312
NM_004656.4(BAP1):c.1027C>G (p.Leu343Val) rs1060503734
NM_004656.4(BAP1):c.1031A>G (p.Asn344Ser) rs142887785
NM_004656.4(BAP1):c.1043C>G (p.Pro348Arg)
NM_004656.4(BAP1):c.1052C>T (p.Thr351Ile) rs1291142030
NM_004656.4(BAP1):c.1058T>C (p.Ile353Thr) rs754217069
NM_004656.4(BAP1):c.1066C>T (p.Arg356Trp) rs761029538
NM_004656.4(BAP1):c.1073C>T (p.Pro358Leu) rs773379358
NM_004656.4(BAP1):c.1132G>A (p.Ala378Thr) rs1559587924
NM_004656.4(BAP1):c.1138G>A (p.Gly380Ser)
NM_004656.4(BAP1):c.1147C>T (p.Arg383Cys) rs201844078
NM_004656.4(BAP1):c.1148G>A (p.Arg383His) rs374620220
NM_004656.4(BAP1):c.1154G>A (p.Arg385Gln) rs765258055
NM_004656.4(BAP1):c.1156G>A (p.Val386Ile)
NM_004656.4(BAP1):c.1165C>T (p.Arg389Cys) rs373809972
NM_004656.4(BAP1):c.1166G>A (p.Arg389His) rs770778299
NM_004656.4(BAP1):c.1168C>A (p.Pro390Thr) rs1425178905
NM_004656.4(BAP1):c.1168C>T (p.Pro390Ser) rs1425178905
NM_004656.4(BAP1):c.1178A>G (p.Gln393Arg) rs772689479
NM_004656.4(BAP1):c.1179G>T (p.Gln393His) rs771803950
NM_004656.4(BAP1):c.1180T>C (p.Tyr394His) rs1060503737
NM_004656.4(BAP1):c.1192G>A (p.Glu398Lys)
NM_004656.4(BAP1):c.1201_1203delinsGAG (p.Tyr401Glu) rs1553645128
NM_004656.4(BAP1):c.1201_1212del (p.Tyr401_Asp404del) rs776606194
NM_004656.4(BAP1):c.1202A>G (p.Tyr401Cys) rs1553645130
NM_004656.4(BAP1):c.1210G>A (p.Asp404Asn) rs1035262201
NM_004656.4(BAP1):c.1212C>G (p.Asp404Glu) rs140998455
NM_004656.4(BAP1):c.1214_1225del (p.Glu405_Asp408del) rs1553645109
NM_004656.4(BAP1):c.1216G>A (p.Glu406Lys) rs748928044
NM_004656.4(BAP1):c.1217A>C (p.Glu406Ala) rs535695655
NM_004656.4(BAP1):c.1217A>T (p.Glu406Val) rs535695655
NM_004656.4(BAP1):c.1218G>T (p.Glu406Asp) rs752703914
NM_004656.4(BAP1):c.1218_1219delinsAA (p.Asp407Asn) rs1553645112
NM_004656.4(BAP1):c.1219G>A (p.Asp407Asn) rs765347562
NM_004656.4(BAP1):c.122+5G>A
NM_004656.4(BAP1):c.1225G>A (p.Val409Met) rs756443059
NM_004656.4(BAP1):c.122G>C (p.Gly41Ala) rs1553646278
NM_004656.4(BAP1):c.123-3C>T rs543305514
NM_004656.4(BAP1):c.1235C>T (p.Thr412Ile) rs760363108
NM_004656.4(BAP1):c.1243G>C (p.Ala415Pro) rs773097896
NM_004656.4(BAP1):c.1249A>G (p.Arg417Gly)
NM_004656.4(BAP1):c.1251-3C>T rs767276752
NM_004656.4(BAP1):c.1251-8C>A
NM_004656.4(BAP1):c.1253A>G (p.Tyr418Cys)
NM_004656.4(BAP1):c.1257G>T (p.Lys419Asn) rs1437342810
NM_004656.4(BAP1):c.1265G>A (p.Gly422Glu) rs1559587197
NM_004656.4(BAP1):c.1268C>G (p.Thr423Arg)
NM_004656.4(BAP1):c.1268C>T (p.Thr423Ile)
NM_004656.4(BAP1):c.1279G>A (p.Gly427Arg) rs1553644999
NM_004656.4(BAP1):c.1280G>A (p.Gly427Glu) rs761183483
NM_004656.4(BAP1):c.1280G>T (p.Gly427Val) rs761183483
NM_004656.4(BAP1):c.1291G>A (p.Gly431Ser) rs915913191
NM_004656.4(BAP1):c.1297G>A (p.Ala433Thr) rs1553644988
NM_004656.4(BAP1):c.129A>G (p.Val43=)
NM_004656.4(BAP1):c.12C>T (p.Gly4=) rs1060503747
NM_004656.4(BAP1):c.1301A>T (p.Asp434Val)
NM_004656.4(BAP1):c.1315G>T (p.Val439Leu) rs1559587112
NM_004656.4(BAP1):c.1331C>T (p.Thr444Ile) rs1290996849
NM_004656.4(BAP1):c.1337A>C (p.Asn446Thr)
NM_004656.4(BAP1):c.1337A>T (p.Asn446Ile) rs751399960
NM_004656.4(BAP1):c.1339G>A (p.Val447Ile) rs762654322
NM_004656.4(BAP1):c.1345G>A (p.Ala449Thr) rs764734266
NM_004656.4(BAP1):c.1349A>G (p.Glu450Gly)
NM_004656.4(BAP1):c.1370A>G (p.Lys457Arg) rs1553644951
NM_004656.4(BAP1):c.1393A>G (p.Ile465Val)
NM_004656.4(BAP1):c.1408G>A (p.Gly470Arg) rs576538858
NM_004656.4(BAP1):c.1411_1412delinsAT (p.Ala471Ile)
NM_004656.4(BAP1):c.1412C>T (p.Ala471Val) rs749456076
NM_004656.4(BAP1):c.1421C>T (p.Pro474Leu) rs770422186
NM_004656.4(BAP1):c.1438A>G (p.Thr480Ala)
NM_004656.4(BAP1):c.1441C>A (p.His481Asn) rs764816701
NM_004656.4(BAP1):c.1442A>G (p.His481Arg) rs150441842
NM_004656.4(BAP1):c.1498G>A (p.Gly500Ser)
NM_004656.4(BAP1):c.1522C>T (p.Arg508Cys) rs951076425
NM_004656.4(BAP1):c.1547C>T (p.Pro516Leu) rs755719248
NM_004656.4(BAP1):c.1550C>A (p.Thr517Lys) rs764748646
NM_004656.4(BAP1):c.1550C>T (p.Thr517Met) rs764748646
NM_004656.4(BAP1):c.1552C>T (p.Arg518Trp) rs775789477
NM_004656.4(BAP1):c.1553G>A (p.Arg518Gln) rs535796204
NM_004656.4(BAP1):c.159C>A (p.Ile53=)
NM_004656.4(BAP1):c.1600G>A (p.Glu534Lys)
NM_004656.4(BAP1):c.1609A>G (p.Ser537Gly) rs747109385
NM_004656.4(BAP1):c.1616T>C (p.Leu539Pro) rs1553644856
NM_004656.4(BAP1):c.1618C>T (p.Arg540Cys)
NM_004656.4(BAP1):c.1619G>A (p.Arg540His)
NM_004656.4(BAP1):c.1628G>A (p.Cys543Tyr) rs907231325
NM_004656.4(BAP1):c.1633C>T (p.Arg545Cys) rs778628881
NM_004656.4(BAP1):c.1634G>A (p.Arg545His) rs71651687
NM_004656.4(BAP1):c.1643G>A (p.Arg548His) rs779877855
NM_004656.4(BAP1):c.1651C>G (p.Arg551Gly) rs755664216
NM_004656.4(BAP1):c.1652G>A (p.Arg551His) rs759448397
NM_004656.4(BAP1):c.1664C>T (p.Pro555Leu)
NM_004656.4(BAP1):c.1669A>G (p.Ile557Val)
NM_004656.4(BAP1):c.1676C>T (p.Thr559Ile) rs1282721599
NM_004656.4(BAP1):c.1678G>C (p.Gly560Arg)
NM_004656.4(BAP1):c.1681C>G (p.Leu561Val) rs1553644818
NM_004656.4(BAP1):c.1687C>T (p.His563Tyr) rs1559586451
NM_004656.4(BAP1):c.1712G>A (p.Ser571Asn) rs909772484
NM_004656.4(BAP1):c.1714C>T (p.Pro572Ser) rs1553644803
NM_004656.4(BAP1):c.1715C>T (p.Pro572Leu) rs1553644798
NM_004656.4(BAP1):c.1721C>A (p.Ala574Glu) rs761596789
NM_004656.4(BAP1):c.1721C>T (p.Ala574Val) rs761596789
NM_004656.4(BAP1):c.1727C>T (p.Thr576Ile) rs374920141
NM_004656.4(BAP1):c.1735G>A (p.Gly579Arg) rs370004702
NM_004656.4(BAP1):c.1742G>C (p.Gly581Ala)
NM_004656.4(BAP1):c.1748C>T (p.Ser583Leu) rs369259771
NM_004656.4(BAP1):c.1751C>A (p.Pro584His) rs374877744
NM_004656.4(BAP1):c.1763C>G (p.Pro588Arg) rs780338105
NM_004656.4(BAP1):c.1769A>T (p.Gln590Leu) rs756472919
NM_004656.4(BAP1):c.1778A>G (p.Gln593Arg) rs1553644733
NM_004656.4(BAP1):c.1781G>C (p.Gly594Ala) rs144172190
NM_004656.4(BAP1):c.1793C>G (p.Pro598Arg)
NM_004656.4(BAP1):c.179G>A (p.Arg60Gln) rs1553646022
NM_004656.4(BAP1):c.1801_1805delinsGAGGT (p.Lys601_Glu602delinsGluVal) rs1060503748
NM_004656.4(BAP1):c.1805A>T (p.Glu602Val) rs144993791
NM_004656.4(BAP1):c.1806G>C (p.Glu602Asp) rs759423683
NM_004656.4(BAP1):c.1810G>A (p.Val604Met) rs369065146
NM_004656.4(BAP1):c.1820C>T (p.Thr607Met) rs770654975
NM_004656.4(BAP1):c.1833G>C (p.Glu611Asp) rs771494475
NM_004656.4(BAP1):c.1837A>C (p.Thr613Pro)
NM_004656.4(BAP1):c.1837A>G (p.Thr613Ala) rs749728488
NM_004656.4(BAP1):c.1840G>A (p.Gly614Arg)
NM_004656.4(BAP1):c.184G>T (p.Val62Phe) rs759957857
NM_004656.4(BAP1):c.1852C>G (p.Pro618Ala) rs1060503728
NM_004656.4(BAP1):c.1873G>A (p.Glu625Lys) rs1482404545
NM_004656.4(BAP1):c.1880A>T (p.Tyr627Phe) rs1060503742
NM_004656.4(BAP1):c.190A>T (p.Thr64Ser) rs1060503733
NM_004656.4(BAP1):c.1912T>C (p.Cys638Arg)
NM_004656.4(BAP1):c.1922C>A (p.Ala641Asp) rs1559585421
NM_004656.4(BAP1):c.1928T>C (p.Ile643Thr) rs376519545
NM_004656.4(BAP1):c.1931C>T (p.Ala644Val) rs551399575
NM_004656.4(BAP1):c.1943C>T (p.Ala648Val) rs755915077
NM_004656.4(BAP1):c.1946G>A (p.Cys649Tyr) rs151308667
NM_004656.4(BAP1):c.1951_1953del (p.Lys651del) rs1226165465
NM_004656.4(BAP1):c.1952A>G (p.Lys651Arg)
NM_004656.4(BAP1):c.1983+6T>C rs1553644657
NM_004656.4(BAP1):c.2026T>C (p.Cys676Arg) rs1060503740
NM_004656.4(BAP1):c.2032T>A (p.Phe678Ile) rs1060503738
NM_004656.4(BAP1):c.2056+1G>C
NM_004656.4(BAP1):c.2056G>A (p.Gly686Ser)
NM_004656.4(BAP1):c.2060T>G (p.Met687Arg)
NM_004656.4(BAP1):c.206C>G (p.Thr69Arg) rs572063023
NM_004656.4(BAP1):c.206C>T (p.Thr69Met) rs572063023
NM_004656.4(BAP1):c.2096G>A (p.Arg699Gln) rs1466334306
NM_004656.4(BAP1):c.2122C>T (p.Arg708Trp) rs1345279795
NM_004656.4(BAP1):c.2159G>A (p.Arg720His)
NM_004656.4(BAP1):c.2164C>T (p.Arg722Cys)
NM_004656.4(BAP1):c.2167C>T (p.Pro723Ser) rs1553644518
NM_004656.4(BAP1):c.2175G>A (p.Lys725=) rs760537008
NM_004656.4(BAP1):c.2189G>A (p.Ter730=) rs771713346
NM_004656.4(BAP1):c.229G>T (p.Val77Leu)
NM_004656.4(BAP1):c.233A>C (p.Asn78Thr) rs1319729011
NM_004656.4(BAP1):c.233A>G (p.Asn78Ser) rs1319729011
NM_004656.4(BAP1):c.249_250delinsAG (p.His84Asp) rs1559591523
NM_004656.4(BAP1):c.250C>T (p.His84Tyr) rs1338231889
NM_004656.4(BAP1):c.256-3C>A rs752536342
NM_004656.4(BAP1):c.272G>A (p.Cys91Tyr) rs1559591264
NM_004656.4(BAP1):c.314G>T (p.Ser105Ile) rs1553645941
NM_004656.4(BAP1):c.316G>A (p.Val106Met) rs754385495
NM_004656.4(BAP1):c.331A>G (p.Thr111Ala) rs1303575075
NM_004656.4(BAP1):c.332C>T (p.Thr111Ile) rs527433244
NM_004656.4(BAP1):c.340C>T (p.Arg114Cys) rs761048859
NM_004656.4(BAP1):c.341G>A (p.Arg114His) rs773494626
NM_004656.4(BAP1):c.356C>G (p.Thr119Ser) rs762084469
NM_004656.4(BAP1):c.358A>G (p.Lys120Glu) rs774573926
NM_004656.4(BAP1):c.361G>C (p.Gly121Arg) rs1559591093
NM_004656.4(BAP1):c.367A>T (p.Ser123Cys)
NM_004656.4(BAP1):c.37+3G>A rs373910684
NM_004656.4(BAP1):c.37+5G>C rs1559593334
NM_004656.4(BAP1):c.375+4G>A rs371114912
NM_004656.4(BAP1):c.389C>T (p.Ala130Val) rs1559590761
NM_004656.4(BAP1):c.404C>T (p.Pro135Leu) rs374928824
NM_004656.4(BAP1):c.405G>A (p.Pro135=) rs768046980
NM_004656.4(BAP1):c.40C>T (p.Leu14Phe) rs1208026193
NM_004656.4(BAP1):c.437+4T>C rs1553645837
NM_004656.4(BAP1):c.448C>T (p.Arg150Cys) rs548946316
NM_004656.4(BAP1):c.449G>A (p.Arg150His)
NM_004656.4(BAP1):c.490A>G (p.Thr164Ala)
NM_004656.4(BAP1):c.50T>C (p.Leu17Pro) rs1060503745
NM_004656.4(BAP1):c.551A>G (p.Asp184Gly) rs1060503729
NM_004656.4(BAP1):c.554G>A (p.Gly185Glu) rs1553645794
NM_004656.4(BAP1):c.566A>G (p.Tyr189Cys)
NM_004656.4(BAP1):c.580+4G>A rs1060503730
NM_004656.4(BAP1):c.580+6C>T rs1553645784
NM_004656.4(BAP1):c.586T>A (p.Trp196Arg) rs1060503746
NM_004656.4(BAP1):c.588G>C (p.Trp196Cys) rs1193212091
NM_004656.4(BAP1):c.588G>T (p.Trp196Cys) rs1193212091
NM_004656.4(BAP1):c.589G>T (p.Gly197Trp) rs1060503739
NM_004656.4(BAP1):c.591G>T (p.Gly197=)
NM_004656.4(BAP1):c.601G>C (p.Glu201Gln)
NM_004656.4(BAP1):c.620G>A (p.Arg207Gln) rs1277247682
NM_004656.4(BAP1):c.623G>A (p.Arg208Gln) rs867416499
NM_004656.4(BAP1):c.626T>C (p.Val209Ala) rs878854740
NM_004656.4(BAP1):c.629T>C (p.Ile210Thr)
NM_004656.4(BAP1):c.638G>A (p.Arg213His) rs1220529268
NM_004656.4(BAP1):c.638G>C (p.Arg213Pro)
NM_004656.4(BAP1):c.649G>A (p.Ala217Thr) rs1553645702
NM_004656.4(BAP1):c.659+3A>C rs878854741
NM_004656.4(BAP1):c.66C>T (p.Phe22=) rs1559593101
NM_004656.4(BAP1):c.67+5G>C rs1033651300
NM_004656.4(BAP1):c.670_672del (p.His224del) rs1337893429
NM_004656.4(BAP1):c.706G>A (p.Asp236Asn) rs1559589762
NM_004656.4(BAP1):c.747G>T (p.Lys249Asn) rs1553645603
NM_004656.4(BAP1):c.748G>A (p.Val250Met)
NM_004656.4(BAP1):c.772G>A (p.Ala258Thr) rs1559589668
NM_004656.4(BAP1):c.779A>G (p.Gln260Arg) rs878854742
NM_004656.4(BAP1):c.789A>G (p.Ile263Met)
NM_004656.4(BAP1):c.797C>T (p.Thr266Ile) rs769338697
NM_004656.4(BAP1):c.809T>C (p.Leu270Pro)
NM_004656.4(BAP1):c.863C>G (p.Ala288Gly)
NM_004656.4(BAP1):c.86T>G (p.Val29Gly) rs1553646295
NM_004656.4(BAP1):c.875C>G (p.Ser292Cys) rs1553645470
NM_004656.4(BAP1):c.878C>T (p.Pro293Leu) rs777664260
NM_004656.4(BAP1):c.881T>G (p.Leu294Arg)
NM_004656.4(BAP1):c.916G>A (p.Glu306Lys) rs779566198
NM_004656.4(BAP1):c.931+4C>G rs1559589067
NM_004656.4(BAP1):c.944A>C (p.Glu315Ala) rs149974450
NM_004656.4(BAP1):c.961G>T (p.Ala321Ser)
NM_004656.4(BAP1):c.982C>G (p.Pro328Ala) rs760860535
NM_004656.4(BAP1):c.989A>G (p.Asn330Ser) rs1553645322
NM_004656.4(BAP1):c.990C>G (p.Asn330Lys)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.