List of variants reported as uncertain significance for BAP1-related tumor predisposition syndrome by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.1555C>T (p.Pro519Ser)	rs759622893	0.00001
NM_004656.4(BAP1):c.1554G>T (p.Arg518=)	rs1705043802
NM_004656.4(BAP1):c.1722_1724delinsACG (p.Leu575Arg)	rs1553644790
NM_004656.4(BAP1):c.31G>A (p.Asp11Asn)	rs1578231322

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