List of variants in gene BARD1 reported by German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1127C>T (p.Ser376Leu)	rs587782333	0.00009
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser)	rs587781976	0.00007
NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr)	rs587780030	0.00004
NM_000465.4(BARD1):c.1533G>A (p.Lys511=)	rs371785856	0.00003
NM_000465.4(BARD1):c.212G>T (p.Cys71Phe)	rs1064793959	0.00003
NM_000465.4(BARD1):c.2002-2A>G	rs876658260	0.00001
NM_000465.4(BARD1):c.1080T>C (p.Pro360=)	rs2106108809
NM_000465.4(BARD1):c.1314G>T (p.Lys438Asn)	rs1559423185
NM_000465.4(BARD1):c.1569-7T>G	rs1559395026
NM_000465.4(BARD1):c.158G>A (p.Cys53Tyr)	rs747582517
NM_000465.4(BARD1):c.159-1G>T	rs879254139
NM_000465.4(BARD1):c.1811-1G>A	rs879253952
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs)	rs587780024
NM_000465.4(BARD1):c.2100C>T (p.Gly700=)	rs1692220418
NM_000465.4(BARD1):c.2203C>T (p.Gln735Ter)	rs767395666
NM_000465.4(BARD1):c.623dup (p.Lys209fs)	rs587780033

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