ClinVar Miner

List of variants in gene BAP1 reported as benign by Illumina Laboratory Services, Illumina

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Total variants: 26
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HGVS dbSNP gnomAD frequency
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.1026C>T (p.Ser342=) rs71651686 0.00304
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.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.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.534C>T (p.Gly178=) rs200285587 0.00016
NM_004656.4(BAP1):c.912C>A (p.Ala304=) rs201809705 0.00016
NM_004656.4(BAP1):c.1735G>A (p.Gly579Arg) rs370004702 0.00013
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.1338C>T (p.Asn446=) rs763735807 0.00005
NM_004656.4(BAP1):c.*1164G>C rs376927338
NM_004656.4(BAP1):c.*45C>G rs56898787
NM_004656.4(BAP1):c.*573G>A rs144145384

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