List of variants reported as pathogenic for BAP1-related tumor predisposition syndrome by OMIM

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.438-2A>G	rs587776879	0.00001
NM_004656.4(BAP1):c.1305del (p.Gln436fs)	rs587776877
NM_004656.4(BAP1):c.1654del (p.Asp552fs)	rs397509414
NM_004656.4(BAP1):c.1717del (p.Leu573fs)	rs869025212
NM_004656.4(BAP1):c.1882_1885del (p.Ser628fs)	rs1559585778
NM_004656.4(BAP1):c.2050C>T (p.Gln684Ter)	rs387906848
NM_004656.4(BAP1):c.2057-2A>G	rs587776878
NM_004656.4(BAP1):c.277A>G (p.Thr93Ala)	rs375129361
NM_004656.4(BAP1):c.78_79del (p.Val27fs)	rs397509413
NM_004656.4(BAP1):c.799C>T (p.Gln267Ter)	rs387906849

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