List of variants in gene BAP1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.1117-1G>A
NM_004656.4(BAP1):c.122+5G>C	rs1578230320
NM_004656.4(BAP1):c.1464dup (p.Ser489fs)
NM_004656.4(BAP1):c.146T>C (p.Leu49Pro)	rs2153228340
NM_004656.4(BAP1):c.1588del (p.Val530fs)	rs2153226657
NM_004656.4(BAP1):c.170G>A (p.Arg57Gln)
NM_004656.4(BAP1):c.1730-1G>A	rs1559586168
NM_004656.4(BAP1):c.176G>A (p.Arg59Gln)	rs1298276806
NM_004656.4(BAP1):c.2057-2A>C
NM_004656.4(BAP1):c.272dup (p.Cys91fs)	rs2153228146
NM_004656.4(BAP1):c.34C>G (p.Pro12Ala)	rs2153228682
NM_004656.4(BAP1):c.358A>T (p.Lys120Ter)	rs774573926
NM_004656.4(BAP1):c.37+1G>T	rs1559593339
NM_004656.4(BAP1):c.375+1G>A
NM_004656.4(BAP1):c.38-2A>G	rs2153228637
NM_004656.4(BAP1):c.458_459del (p.Pro153fs)	rs1559590613
NM_004656.4(BAP1):c.586dup (p.Trp196fs)	rs1553645728
NM_004656.4(BAP1):c.592dup (p.Glu198fs)	rs1205668341
NM_004656.4(BAP1):c.659+1del	rs1064795667
NM_004656.4(BAP1):c.91G>A (p.Glu31Lys)	rs2153228535
NM_004656.4(BAP1):c.932-2_933del	rs2153227087

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