ClinVar Miner

Variants in gene BAP1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 22
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HGVS dbSNP
NM_004656.3(BAP1):c.-10C>T rs200018055
NM_004656.3(BAP1):c.1002A>G (p.Leu334=) rs28997577
NM_004656.3(BAP1):c.1026C>T (p.Ser342=) rs71651686
NM_004656.3(BAP1):c.1035G>C (p.Gly345=) rs369744075
NM_004656.3(BAP1):c.1212C>G (p.Asp404Glu) rs140998455
NM_004656.3(BAP1):c.121G>A (p.Gly41Ser) rs372586694
NM_004656.3(BAP1):c.1268C>A (p.Thr423Lys) rs115109161
NM_004656.3(BAP1):c.1320G>A (p.Leu440=) rs77722216
NM_004656.3(BAP1):c.1729+8T>C rs150945583
NM_004656.3(BAP1):c.1838C>T (p.Thr613Met) rs35448940
NM_004656.3(BAP1):c.1962A>C (p.Val654=) rs148624125
NM_004656.3(BAP1):c.2057-4G>T rs149499021
NM_004656.3(BAP1):c.288G>A (p.Leu96=) rs117382883
NM_004656.3(BAP1):c.501G>A (p.Ala167=) rs148631953
NM_004656.3(BAP1):c.519T>C (p.Tyr173=) rs143901408
NM_004656.3(BAP1):c.534C>T (p.Gly178=) rs200285587
NM_004656.3(BAP1):c.651C>T (p.Ala217=) rs202170860
NM_004656.3(BAP1):c.672C>T (p.His224=) rs756217463
NM_004656.3(BAP1):c.783G>A (p.Gln261=) rs35003777
NM_004656.3(BAP1):c.869A>G (p.Asn290Ser) rs747079481
NM_004656.3(BAP1):c.912C>A (p.Ala304=) rs201809705
NM_004656.3(BAP1):c.960C>T (p.Cys320=) rs143659795

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