List of variants in gene BAG3 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.187C>G (p.Pro63Ala)	rs144041999	0.00311
NM_004281.4(BAG3):c.1138C>T (p.Pro380Ser)	rs144692954	0.00310
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr)	rs61756328	0.00239
NM_004281.4(BAG3):c.25A>G (p.Met9Val)	rs137965903	0.00175
NM_004281.4(BAG3):c.1587C>T (p.Ala529=)	rs149358702	0.00144
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe)	rs145393807	0.00075
NM_004281.4(BAG3):c.870C>G (p.Pro290=)	rs140737221	0.00055
NM_004281.4(BAG3):c.855G>A (p.Thr285=)	rs147259596	0.00048
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu)	rs143919208	0.00035
NM_004281.4(BAG3):c.771C>T (p.Pro257=)	rs200212999	0.00027
NM_004281.4(BAG3):c.898G>A (p.Asp300Asn)	rs78439745	0.00026
NM_004281.4(BAG3):c.653G>A (p.Arg218Gln)	rs201638005	0.00018
NM_004281.4(BAG3):c.96G>T (p.Pro32=)	rs372083121	0.00017
NM_004281.4(BAG3):c.415C>T (p.Arg139Trp)	rs556465096	0.00011
NM_004281.4(BAG3):c.636C>T (p.His212=)	rs150379892	0.00007
NM_004281.4(BAG3):c.785C>T (p.Ala262Val)	rs397516883	0.00006
NM_004281.4(BAG3):c.679C>G (p.Gln227Glu)	rs149517238	0.00004
NM_004281.4(BAG3):c.337G>A (p.Val113Ile)	rs781093275	0.00002
NM_004281.4(BAG3):c.1202C>G (p.Ala401Gly)	rs775153939	0.00001
NM_004281.4(BAG3):c.1344C>T (p.Asp448=)	rs727504796	0.00001
NM_004281.4(BAG3):c.306C>T (p.Gly102=)	rs202006167	0.00001
NM_004281.4(BAG3):c.465A>G (p.Ala155=)	rs775151738	0.00001
NM_004281.4(BAG3):c.873G>A (p.Ser291=)	rs1387744249	0.00001
NM_004281.4(BAG3):c.180+5701G>A	rs141277536
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)	rs35434411
NM_004281.4(BAG3):c.468GGC[4] (p.Ala160dup)	rs139438727
NM_004281.4(BAG3):c.537C>T (p.Cys179=)

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