List of variants in gene BAP1 reported as not provided

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.1786A>G (p.Ser596Gly)	rs79014342	0.02383
NM_004656.4(BAP1):c.1838C>T (p.Thr613Met)	rs35448940	0.00377
NM_004656.4(BAP1):c.905C>T (p.Pro302Leu)	rs149158790	0.00041
NM_004656.4(BAP1):c.1735G>A (p.Gly579Arg)	rs370004702	0.00013
NM_004656.4(BAP1):c.1408G>A (p.Gly470Arg)	rs576538858	0.00012
NM_004656.4(BAP1):c.121G>A (p.Gly41Ser)	rs372586694	0.00009
NM_004656.4(BAP1):c.1251-1G>C	rs1578221396
NM_004656.4(BAP1):c.1325C>G (p.Pro442Arg)	rs587778089
NM_004656.4(BAP1):c.2100del (p.Arg701fs)	rs2153226109
NM_004656.4(BAP1):c.271T>C (p.Cys91Arg)	rs1705222655
NM_004656.4(BAP1):c.660-2A>G	rs1559589809
NM_004656.4(BAP1):c.932-1G>T	rs9848343

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