List of variants in gene BARD1 reported as pathogenic by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status:		Collection method:
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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1216C>T (p.Arg406Ter)	rs377153250	0.00003
NM_000465.4(BARD1):c.1690C>T (p.Gln564Ter)	rs587780021	0.00003
NM_000465.4(BARD1):c.1921C>T (p.Arg641Ter)	rs587781948	0.00003
NM_000465.4(BARD1):c.1652C>G (p.Ser551Ter)	rs587781707	0.00001
NM_000465.4(BARD1):c.334C>T (p.Arg112Ter)	rs758972589	0.00001
NM_000465.4(BARD1):c.448C>T (p.Arg150Ter)	rs730881411	0.00001
GRCh37/hg19 2q35(chr2:215557511-215623955)x1
NM_000465.4(BARD1):c.1314+1G>A	rs753785671
NM_000465.4(BARD1):c.159-1G>T	rs879254139
NM_000465.4(BARD1):c.1904-1G>A	rs2469277929
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs)	rs587780024
NM_000465.4(BARD1):c.258T>A (p.Cys86Ter)	rs749378322
NM_000465.4(BARD1):c.298C>T (p.Gln100Ter)	rs786201912
NM_000465.4(BARD1):c.496C>T (p.Gln166Ter)	rs786202500
NM_000465.4(BARD1):c.539_540del (p.Ser179_Tyr180insTer)	rs779427628
NM_000465.4(BARD1):c.55G>T (p.Glu19Ter)	rs752514155
NM_000465.4(BARD1):c.623dup (p.Lys209fs)	rs587780033

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