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
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.