ClinVar Miner

List of variants in gene BAP1 reported as benign

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_004656.4(BAP1):c.255+136C>G rs123602 0.18875
NM_004656.4(BAP1):c.1786A>G (p.Ser596Gly) rs79014342 0.02383
NM_004656.4(BAP1):c.1413T>G (p.Ala471=) rs34736117 0.01973
NM_004656.4(BAP1):c.*974C>T rs9855479 0.01794
NM_004656.4(BAP1):c.*392C>T rs112026686 0.00839
NM_004656.4(BAP1):c.2057-4G>T rs149499021 0.00433
NM_004656.4(BAP1):c.1838C>T (p.Thr613Met) rs35448940 0.00377
NM_004656.4(BAP1):c.783G>A (p.Gln261=) rs35003777 0.00377
NM_004656.4(BAP1):c.1729+8T>C rs150945583 0.00364
NM_004656.4(BAP1):c.1891-30G>C rs146661777 0.00328
NM_004656.4(BAP1):c.1002A>G (p.Leu334=) rs28997577 0.00310
NM_004656.4(BAP1):c.1026C>T (p.Ser342=) rs71651686 0.00304
NM_004656.4(BAP1):c.1250+42G>A rs150454901 0.00257
NM_004656.4(BAP1):c.2057-22A>C rs144083199 0.00246
NM_004656.4(BAP1):c.123-48T>G rs143273211 0.00235
NM_004656.4(BAP1):c.960C>T (p.Cys320=) rs143659795 0.00234
NM_004656.4(BAP1):c.*385A>T rs143014714 0.00187
NM_004656.4(BAP1):c.1268C>A (p.Thr423Lys) rs115109161 0.00166
NM_004656.4(BAP1):c.*300A>G rs150842955 0.00148
NM_004656.4(BAP1):c.*37G>A rs139307137 0.00147
NM_004656.4(BAP1):c.659+11T>C rs199926938 0.00094
NM_004656.4(BAP1):c.519T>C (p.Tyr173=) rs143901408 0.00059
NM_004656.4(BAP1):c.1320G>A (p.Leu440=) rs77722216 0.00056
NM_004656.4(BAP1):c.294C>T (p.Ser98=) rs140641333 0.00056
NM_004656.4(BAP1):c.501G>A (p.Ala167=) rs148631953 0.00050
NM_004656.4(BAP1):c.1427T>C (p.Val476Ala) rs144060813 0.00044
NM_004656.4(BAP1):c.905C>T (p.Pro302Leu) rs149158790 0.00041
NM_004656.4(BAP1):c.288G>A (p.Leu96=) rs117382883 0.00037
NM_004656.4(BAP1):c.1035G>C (p.Gly345=) rs369744075 0.00035
NM_004656.4(BAP1):c.1962A>C (p.Val654=) rs148624125 0.00031
NM_004656.4(BAP1):c.376-4G>A rs369277958 0.00016
NM_004656.4(BAP1):c.534C>T (p.Gly178=) rs200285587 0.00016
NM_004656.4(BAP1):c.651C>T (p.Ala217=) rs202170860 0.00016
NM_004656.4(BAP1):c.672C>T (p.His224=) rs756217463 0.00016
NM_004656.4(BAP1):c.912C>A (p.Ala304=) rs201809705 0.00016
NM_004656.4(BAP1):c.2091C>T (p.Ser697=) rs754513396 0.00014
NM_004656.4(BAP1):c.1735G>A (p.Gly579Arg) rs370004702 0.00013
NM_004656.4(BAP1):c.1212C>G (p.Asp404Glu) rs140998455 0.00011
NM_004656.4(BAP1):c.*643G>A rs374367093 0.00010
NM_004656.4(BAP1):c.-10C>T rs200018055 0.00009
NM_004656.4(BAP1):c.121G>A (p.Gly41Ser) rs372586694 0.00009
NM_004656.4(BAP1):c.1609A>G (p.Ser537Gly) rs747109385 0.00009
NM_004656.4(BAP1):c.1872G>A (p.Gly624=) rs375950004 0.00009
NM_004656.4(BAP1):c.2013C>T (p.Tyr671=) rs200194082 0.00009
NM_004656.4(BAP1):c.869A>G (p.Asn290Ser) rs747079481 0.00008
NM_004656.4(BAP1):c.37+31G>C rs200628603 0.00006
NM_004656.4(BAP1):c.1338C>T (p.Asn446=) rs763735807 0.00005
NM_004656.4(BAP1):c.659+17T>A rs753960146 0.00004
NM_004656.4(BAP1):c.878C>T (p.Pro293Leu) rs777664260 0.00004
NM_004656.4(BAP1):c.1217A>T (p.Glu406Val) rs535695655 0.00003
NM_004656.4(BAP1):c.1890+11G>A rs537090290 0.00003
NM_004656.4(BAP1):c.1551G>A (p.Thr517=) rs145158446 0.00002
NM_004656.4(BAP1):c.924C>T (p.Asn308=) rs749945143 0.00002
NM_004656.4(BAP1):c.1956G>A (p.Glu652=) rs761399207 0.00001
NM_004656.4(BAP1):c.360G>A (p.Lys120=) rs749405309 0.00001
NM_004656.4(BAP1):c.375+12T>A rs564875789 0.00001
NM_004656.4(BAP1):c.572T>C (p.Ile191Thr) rs752793866 0.00001
NM_004656.4(BAP1):c.*1164G>C rs376927338
NM_004656.4(BAP1):c.*45C>G rs56898787
NM_004656.4(BAP1):c.*573G>A rs144145384
NM_004656.4(BAP1):c.1201_1212del (p.Tyr401_Asp404del) rs776606194
NM_004656.4(BAP1):c.1801A>G (p.Lys601Glu) rs142059527
NM_004656.4(BAP1):c.1805A>T (p.Glu602Val) rs144993791
NM_004656.4(BAP1):c.1983+20del
NM_004656.4(BAP1):c.37+44G>C
NM_004656.4(BAP1):c.376-5del rs1705203760
NM_004656.4(BAP1):c.67+13del
NM_004656.4(BAP1):c.931+6dup rs1553645439

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