ClinVar Miner

List of variants in gene BAP1 reported as likely benign for not specified

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Gene type:
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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_004656.4(BAP1):c.2057-4G>T rs149499021 0.00433
NM_004656.4(BAP1):c.1729+8T>C rs150945583 0.00364
NM_004656.4(BAP1):c.660-26T>A rs139414598 0.00328
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.960C>T (p.Cys320=) rs143659795 0.00234
NM_004656.4(BAP1):c.*37G>A rs139307137 0.00147
NM_004656.4(BAP1):c.931+36A>T rs376200445 0.00108
NM_004656.4(BAP1):c.519T>C (p.Tyr173=) rs143901408 0.00059
NM_004656.4(BAP1):c.294C>T (p.Ser98=) rs140641333 0.00056
NM_004656.4(BAP1):c.376-50C>T rs370668123 0.00055
NM_004656.4(BAP1):c.501G>A (p.Ala167=) rs148631953 0.00050
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.1407C>T (p.Ser469=) rs150524807 0.00015
NM_004656.4(BAP1):c.659+18G>T rs377298140 0.00015
NM_004656.4(BAP1):c.879G>A (p.Pro293=) rs200787553 0.00013
NM_004656.4(BAP1):c.1116+40C>T rs373554042 0.00009
NM_004656.4(BAP1):c.1872G>A (p.Gly624=) rs375950004 0.00009
NM_004656.4(BAP1):c.642C>T (p.Ile214=) rs200953639 0.00008
NM_004656.4(BAP1):c.1116+50G>A rs756419402 0.00006
NM_004656.4(BAP1):c.37+31G>C rs200628603 0.00006
NM_004656.4(BAP1):c.255+22G>C rs761358401 0.00004
NM_004656.4(BAP1):c.1224C>T (p.Asp408=) rs755110121 0.00003
NM_004656.4(BAP1):c.1890+11G>A rs537090290 0.00003
NM_004656.4(BAP1):c.1944G>A (p.Ala648=) rs150494756 0.00003
NM_004656.4(BAP1):c.255+6_255+7insA rs778194859 0.00003
NM_004656.4(BAP1):c.38-11G>A rs768279336 0.00003
NM_004656.4(BAP1):c.705C>T (p.Pro235=) rs138180791 0.00003
NM_004656.4(BAP1):c.783+12T>G rs749694454 0.00003
NM_004656.4(BAP1):c.783+15T>G rs769511685 0.00003
NM_004656.4(BAP1):c.210C>T (p.Ser70=) rs558581070 0.00002
NM_004656.4(BAP1):c.648C>T (p.Leu216=) rs758650064 0.00002
NM_004656.4(BAP1):c.126T>C (p.Pro42=) rs1156967472 0.00001
NM_004656.4(BAP1):c.1387C>T (p.Leu463=) rs145361939 0.00001
NM_004656.4(BAP1):c.2145T>C (p.Pro715=) rs1057522124 0.00001
NM_004656.4(BAP1):c.423T>C (p.His141=) rs757571975 0.00001
NM_004656.4(BAP1):c.437+18G>A rs1157072290 0.00001
NM_004656.4(BAP1):c.54C>T (p.Leu18=) rs769459561 0.00001
NM_004656.4(BAP1):c.581-4C>T rs1578225974 0.00001
NM_004656.4(BAP1):c.67+46C>T rs775402861 0.00001
NM_004656.4(BAP1):c.720G>A (p.Lys240=) rs1379682858 0.00001
NM_004656.4(BAP1):c.*17C>G
NM_004656.4(BAP1):c.1065G>A (p.Gln355=)
NM_004656.4(BAP1):c.1117-40G>A rs145366930
NM_004656.4(BAP1):c.1218G>A (p.Glu406=)
NM_004656.4(BAP1):c.1299T>C (p.Ala433=) rs1553644986
NM_004656.4(BAP1):c.1708C>T (p.Leu570=) rs1553644806
NM_004656.4(BAP1):c.1729+39C>G
NM_004656.4(BAP1):c.1730-42T>G
NM_004656.4(BAP1):c.1890+11G>C rs537090290
NM_004656.4(BAP1):c.1891-39G>A rs371637639
NM_004656.4(BAP1):c.1891-39G>C
NM_004656.4(BAP1):c.189T>C (p.Ser63=) rs1553646013
NM_004656.4(BAP1):c.2056+27T>C
NM_004656.4(BAP1):c.2056+47C>T
NM_004656.4(BAP1):c.2057-16C>T rs369116884
NM_004656.4(BAP1):c.256-49dup rs2153228191
NM_004656.4(BAP1):c.37+12A>G
NM_004656.4(BAP1):c.37+35A>T
NM_004656.4(BAP1):c.376-23C>T
NM_004656.4(BAP1):c.376-38G>T
NM_004656.4(BAP1):c.376-46C>T
NM_004656.4(BAP1):c.38-41C>G
NM_004656.4(BAP1):c.38-6A>T rs1578230960
NM_004656.4(BAP1):c.437+15_437+23del rs755685938
NM_004656.4(BAP1):c.528C>T (p.Ile176=) rs1057522989
NM_004656.4(BAP1):c.581-16T>C rs573678535
NM_004656.4(BAP1):c.581-28G>A
NM_004656.4(BAP1):c.581-43C>T
NM_004656.4(BAP1):c.67+26C>A
NM_004656.4(BAP1):c.67+27C>T rs539725123
NM_004656.4(BAP1):c.68-26C>T
NM_004656.4(BAP1):c.784-14G>T rs1057523584
NM_004656.4(BAP1):c.784-27C>T
NM_004656.4(BAP1):c.931+43C>T

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