ClinVar Miner

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

Included ClinVar conditions (1):
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Total variants: 55
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HGVS dbSNP
NM_000267.3(NF1):c.1810T>C (p.Leu604=) rs142712751
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.121G>A (p.Gly41Ser) rs372586694
NM_004656.4(BAP1):c.1227G>C (p.Val409=) rs201203425
NM_004656.4(BAP1):c.1251-7C>T rs756136482
NM_004656.4(BAP1):c.1268C>A (p.Thr423Lys) rs115109161
NM_004656.4(BAP1):c.1338C>T (p.Asn446=) rs763735807
NM_004656.4(BAP1):c.1527G>A (p.Ser509=) rs756500771
NM_004656.4(BAP1):c.1551G>A (p.Thr517=) rs145158446
NM_004656.4(BAP1):c.162A>G (p.Glu54=) rs1553646029
NM_004656.4(BAP1):c.1729+8T>C rs150945583
NM_004656.4(BAP1):c.174C>G (p.Ser58=) rs776102639
NM_004656.4(BAP1):c.1838C>T (p.Thr613Met) rs35448940
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.1890+10C>T rs776553452
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.2016T>C (p.Asp672=) rs1553644629
NM_004656.4(BAP1):c.2057-4G>T rs149499021
NM_004656.4(BAP1):c.2076G>A (p.Val692=) rs747712653
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.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.38-7del rs775275930
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.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.688C>T (p.Leu230=) rs150084170
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.903C>T (p.Ala301=) rs1553645454
NM_004656.4(BAP1):c.931+10G>C rs199560386
NM_004656.4(BAP1):c.931+8G>A rs573724882
NM_004656.4(BAP1):c.960C>T (p.Cys320=) rs143659795
NM_004656.4(BAP1):c.96C>T (p.Ile32=) rs1223222289

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