ClinVar Miner

List of variants reported as benign for BAP1-related tumor predisposition syndrome by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
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Total variants: 26
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HGVS dbSNP
NM_004656.4(BAP1):c.*1164G>C rs376927338
NM_004656.4(BAP1):c.*300A>G
NM_004656.4(BAP1):c.*37G>A rs139307137
NM_004656.4(BAP1):c.*385A>T
NM_004656.4(BAP1):c.*392C>T
NM_004656.4(BAP1):c.*45C>G rs56898787
NM_004656.4(BAP1):c.*573G>A
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.1026C>T (p.Ser342=) rs71651686
NM_004656.4(BAP1):c.1035G>C (p.Gly345=) rs369744075
NM_004656.4(BAP1):c.121G>A (p.Gly41Ser) rs372586694
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.1413T>G (p.Ala471=) rs34736117
NM_004656.4(BAP1):c.1427T>C (p.Val476Ala) rs144060813
NM_004656.4(BAP1):c.1735G>A (p.Gly579Arg) rs370004702
NM_004656.4(BAP1):c.1786A>G (p.Ser596Gly) rs79014342
NM_004656.4(BAP1):c.1962A>C (p.Val654=) rs148624125
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.501G>A (p.Ala167=) rs148631953
NM_004656.4(BAP1):c.534C>T (p.Gly178=) rs200285587
NM_004656.4(BAP1):c.912C>A (p.Ala304=) rs201809705
NM_004656.4(BAP1):c.960C>T (p.Cys320=) rs143659795

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