ClinVar Miner

List of variants in gene BAP1 reported as likely benign for BAP1-related tumor predisposition syndrome

Included ClinVar conditions (1):
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Gene type:
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Total variants: 124
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HGVS dbSNP
NM_004656.4(BAP1):c.*1164G>C rs376927338
NM_004656.4(BAP1):c.*37G>A rs139307137
NM_004656.4(BAP1):c.*444C>T rs123598
NM_004656.4(BAP1):c.*643G>A rs374367093
NM_004656.4(BAP1):c.*974C>T rs9855479
NM_004656.4(BAP1):c.-10C>T rs200018055
NM_004656.4(BAP1):c.1002A>G (p.Leu334=) rs28997577
NM_004656.4(BAP1):c.1026C>T (p.Ser342=) rs71651686
NM_004656.4(BAP1):c.1029C>T (p.Leu343=) rs1553645304
NM_004656.4(BAP1):c.102C>T (p.Asp34=) rs374877961
NM_004656.4(BAP1):c.1035G>C (p.Gly345=) rs369744075
NM_004656.4(BAP1):c.1117-5C>T rs771441619
NM_004656.4(BAP1):c.1131G>A (p.Leu377=) rs572089064
NM_004656.4(BAP1):c.1200C>T (p.Asp400=) rs1060505013
NM_004656.4(BAP1):c.121G>A (p.Gly41Ser) rs372586694
NM_004656.4(BAP1):c.1221T>C (p.Asp407=) rs1028053412
NM_004656.4(BAP1):c.1224C>T (p.Asp408=) rs755110121
NM_004656.4(BAP1):c.1227G>C (p.Val409=) rs201203425
NM_004656.4(BAP1):c.1250+7C>G rs878854738
NM_004656.4(BAP1):c.1251-7C>T rs756136482
NM_004656.4(BAP1):c.1251-8C>T rs766385310
NM_004656.4(BAP1):c.1268C>A (p.Thr423Lys) rs115109161
NM_004656.4(BAP1):c.1308A>G (p.Gln436=) rs202038162
NM_004656.4(BAP1):c.1330A>G (p.Thr444Ala) rs374746213
NM_004656.4(BAP1):c.1338C>T (p.Asn446=) rs763735807
NM_004656.4(BAP1):c.1344G>A (p.Leu448=) rs368684241
NM_004656.4(BAP1):c.1387C>T (p.Leu463=) rs145361939
NM_004656.4(BAP1):c.1407C>T (p.Ser469=) rs150524807
NM_004656.4(BAP1):c.1416G>A (p.Gly472=) rs375433595
NM_004656.4(BAP1):c.1422G>A (p.Pro474=) rs199888129
NM_004656.4(BAP1):c.1427T>C (p.Val476Ala) rs144060813
NM_004656.4(BAP1):c.1461C>T (p.Thr487=) rs762466375
NM_004656.4(BAP1):c.1485G>A (p.Thr495=) rs368369242
NM_004656.4(BAP1):c.1497C>T (p.Ile499=) rs777417522
NM_004656.4(BAP1):c.1527G>A (p.Ser509=) rs756500771
NM_004656.4(BAP1):c.1536C>T (p.Arg512=) rs754653135
NM_004656.4(BAP1):c.1542C>T (p.Ala514=) rs1553644891
NM_004656.4(BAP1):c.1548G>A (p.Pro516=) rs148990823
NM_004656.4(BAP1):c.1551G>A (p.Thr517=) rs145158446
NM_004656.4(BAP1):c.159C>T (p.Ile53=) rs187643606
NM_004656.4(BAP1):c.162A>G (p.Glu54=) rs1553646029
NM_004656.4(BAP1):c.1716C>T (p.Pro572=) rs1240647699
NM_004656.4(BAP1):c.1722G>A (p.Ala574=) rs774348167
NM_004656.4(BAP1):c.1725G>A (p.Leu575=) rs748508800
NM_004656.4(BAP1):c.1729+8T>C rs150945583
NM_004656.4(BAP1):c.1749G>A (p.Ser583=) rs147775249
NM_004656.4(BAP1):c.174C>G (p.Ser58=) rs776102639
NM_004656.4(BAP1):c.177G>A (p.Arg59=) rs770446947
NM_004656.4(BAP1):c.1791C>T (p.Ser597=) rs751730111
NM_004656.4(BAP1):c.1821G>A (p.Thr607=) rs752063900
NM_004656.4(BAP1):c.1824C>T (p.Asp608=) rs1553644721
NM_004656.4(BAP1):c.1838C>T (p.Thr613Met) rs35448940
NM_004656.4(BAP1):c.1839G>A (p.Thr613=) rs756450018
NM_004656.4(BAP1):c.1842G>A (p.Gly614=) rs781269263
NM_004656.4(BAP1):c.1842G>C (p.Gly614=) rs781269263
NM_004656.4(BAP1):c.186C>T (p.Val62=) rs199608453
NM_004656.4(BAP1):c.1872G>A (p.Gly624=) rs375950004
NM_004656.4(BAP1):c.1890+10C>T rs776553452
NM_004656.4(BAP1):c.1890+9C>G rs1553644699
NM_004656.4(BAP1):c.1944G>A (p.Ala648=) rs150494756
NM_004656.4(BAP1):c.1947C>T (p.Cys649=) rs1041287605
NM_004656.4(BAP1):c.1962A>C (p.Val654=) rs148624125
NM_004656.4(BAP1):c.1983+8A>G rs1271117477
NM_004656.4(BAP1):c.1984-9C>G rs1482074290
NM_004656.4(BAP1):c.2013C>T (p.Tyr671=) rs200194082
NM_004656.4(BAP1):c.2016T>C (p.Asp672=) rs1553644629
NM_004656.4(BAP1):c.2056+7G>A rs547941257
NM_004656.4(BAP1):c.2057-4G>T rs149499021
NM_004656.4(BAP1):c.2070C>T (p.Asn690=) rs1553644559
NM_004656.4(BAP1):c.2076G>A (p.Val692=) rs747712653
NM_004656.4(BAP1):c.207G>A (p.Thr69=) rs748256162
NM_004656.4(BAP1):c.2091C>T (p.Ser697=) rs754513396
NM_004656.4(BAP1):c.2103C>T (p.Arg701=) rs757780962
NM_004656.4(BAP1):c.2118C>T (p.Ile706=) rs201122466
NM_004656.4(BAP1):c.216T>C (p.Ile72=) rs1257200755
NM_004656.4(BAP1):c.288G>A (p.Leu96=) rs117382883
NM_004656.4(BAP1):c.294C>T (p.Ser98=) rs140641333
NM_004656.4(BAP1):c.315C>T (p.Ser105=) rs576176888
NM_004656.4(BAP1):c.333C>T (p.Thr111=) rs375700254
NM_004656.4(BAP1):c.341G>A (p.Arg114His) rs773494626
NM_004656.4(BAP1):c.360G>A (p.Lys120=) rs749405309
NM_004656.4(BAP1):c.37+9G>A rs1440785228
NM_004656.4(BAP1):c.376-4G>A rs369277958
NM_004656.4(BAP1):c.376-5C>T rs776641550
NM_004656.4(BAP1):c.38-7del rs775275930
NM_004656.4(BAP1):c.384A>C (p.Gly128=) rs777514791
NM_004656.4(BAP1):c.437+9G>C rs917909103
NM_004656.4(BAP1):c.438-7T>C rs1374417579
NM_004656.4(BAP1):c.441C>T (p.Pro147=) rs768015706
NM_004656.4(BAP1):c.477T>C (p.Leu159=) rs1417121937
NM_004656.4(BAP1):c.48C>T (p.Thr16=) rs774965502
NM_004656.4(BAP1):c.501G>A (p.Ala167=) rs148631953
NM_004656.4(BAP1):c.534C>T (p.Gly178=) rs200285587
NM_004656.4(BAP1):c.54C>T (p.Leu18=) rs769459561
NM_004656.4(BAP1):c.580+8C>T rs985748596
NM_004656.4(BAP1):c.581-9C>G rs878854739
NM_004656.4(BAP1):c.597C>T (p.Asp199=) rs747458975
NM_004656.4(BAP1):c.642C>T (p.Ile214=) rs200953639
NM_004656.4(BAP1):c.648C>T (p.Leu216=) rs758650064
NM_004656.4(BAP1):c.659+10C>T rs778976365
NM_004656.4(BAP1):c.660-10G>A rs749460317
NM_004656.4(BAP1):c.675C>T (p.Asp225=) rs961974192
NM_004656.4(BAP1):c.681C>T (p.Arg227=) rs772237661
NM_004656.4(BAP1):c.688C>T (p.Leu230=) rs150084170
NM_004656.4(BAP1):c.6T>C (p.Asn2=) rs753081347
NM_004656.4(BAP1):c.705C>T (p.Pro235=) rs138180791
NM_004656.4(BAP1):c.738T>C (p.His246=) rs373722238
NM_004656.4(BAP1):c.744G>A (p.Leu248=) rs762742357
NM_004656.4(BAP1):c.765A>G (p.Val255=) rs1222530223
NM_004656.4(BAP1):c.783G>A (p.Gln261=) rs35003777
NM_004656.4(BAP1):c.795A>G (p.Val265=) rs1553645516
NM_004656.4(BAP1):c.810G>C (p.Leu270=) rs1009864663
NM_004656.4(BAP1):c.821A>C (p.His274Pro) rs565400314
NM_004656.4(BAP1):c.869A>G (p.Asn290Ser) rs747079481
NM_004656.4(BAP1):c.879G>A (p.Pro293=) rs200787553
NM_004656.4(BAP1):c.903C>T (p.Ala301=) rs1553645454
NM_004656.4(BAP1):c.905C>T (p.Pro302Leu) rs149158790
NM_004656.4(BAP1):c.924C>T (p.Asn308=) rs749945143
NM_004656.4(BAP1):c.931+10G>C rs199560386
NM_004656.4(BAP1):c.931+8G>A rs573724882
NM_004656.4(BAP1):c.932-8T>C rs878854743
NM_004656.4(BAP1):c.948G>A (p.Ala316=) rs776898908
NM_004656.4(BAP1):c.960C>T (p.Cys320=) rs143659795
NM_004656.4(BAP1):c.96C>T (p.Ile32=) rs1223222289

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