List of variants in gene BARD1 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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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: 38

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.841C>T (p.Pro281Ser)	rs200059956	0.00005
NM_000465.4(BARD1):c.233G>A (p.Cys78Tyr)	rs199780731	0.00004
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr)	rs146223579	0.00004
NM_000465.4(BARD1):c.1163T>C (p.Ile388Thr)	rs748322604	0.00003
NM_000465.4(BARD1):c.1904-5G>A	rs376639978	0.00003
NM_000465.4(BARD1):c.212G>T (p.Cys71Phe)	rs1064793959	0.00003
NM_000465.4(BARD1):c.556A>G (p.Ser186Gly)	rs16852741	0.00002
NM_000465.4(BARD1):c.1346A>G (p.Gln449Arg)	rs916069875	0.00001
NM_000465.4(BARD1):c.2029T>C (p.Phe677Leu)	rs746790711	0.00001
NM_000465.4(BARD1):c.2251C>T (p.Arg751Trp)	rs139785364	0.00001
NM_000465.4(BARD1):c.427A>G (p.Ile143Val)	rs1060501289	0.00001
NM_000465.4(BARD1):c.465A>G (p.Arg155=)	rs730881413	0.00001
NM_000465.4(BARD1):c.95G>T (p.Gly32Val)	rs587782675	0.00001
NM_000465.4(BARD1):c.1118G>A (p.Gly373Asp)	rs568305044
NM_000465.4(BARD1):c.112C>T (p.Arg38Cys)	rs1553628385
NM_000465.4(BARD1):c.1153G>A (p.Asp385Asn)	rs587782436
NM_000465.4(BARD1):c.128G>C (p.Arg43Pro)	rs1060501305
NM_000465.4(BARD1):c.1309A>G (p.Ile437Val)	rs764592698
NM_000465.4(BARD1):c.1352G>A (p.Gly451Glu)	rs771410310
NM_000465.4(BARD1):c.1429G>A (p.Val477Met)	rs1024564785
NM_000465.4(BARD1):c.1490C>T (p.Pro497Leu)
NM_000465.4(BARD1):c.1513G>A (p.Gly505Arg)	rs864622240
NM_000465.4(BARD1):c.1569-7T>G	rs1559395026
NM_000465.4(BARD1):c.158G>A (p.Cys53Tyr)	rs747582517
NM_000465.4(BARD1):c.1614T>G (p.Ser538Arg)
NM_000465.4(BARD1):c.1703G>C (p.Gly568Ala)	rs1007761710
NM_000465.4(BARD1):c.1819GTT[2] (p.Val609del)	rs927014703
NM_000465.4(BARD1):c.2002-2A>G	rs876658260
NM_000465.4(BARD1):c.216-3A>T	rs1329481396
NM_000465.4(BARD1):c.2188C>A (p.Gln730Lys)	rs1559372004
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638
NM_000465.4(BARD1):c.277C>A (p.Gln93Lys)	rs876658571
NM_000465.4(BARD1):c.30_44del (p.Gln11_Arg15del)	rs587781297
NM_000465.4(BARD1):c.401A>G (p.Asn134Ser)	rs1559426297
NM_000465.4(BARD1):c.485C>T (p.Ser162Leu)	rs755693106
NM_000465.4(BARD1):c.570T>A (p.Asp190Glu)	rs2106111710
NM_000465.4(BARD1):c.661G>C (p.Glu221Gln)	rs1695005056
NM_000465.4(BARD1):c.877A>G (p.Ser293Gly)

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