ClinVar Miner

List of variants in gene BAG3 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_004281.3(BAG3):c.111C>T (p.Pro37=) rs397516880
NM_004281.3(BAG3):c.114C>T (p.Phe38=) rs727504929
NM_004281.3(BAG3):c.1344C>T (p.Asp448=) rs727504796
NM_004281.3(BAG3):c.1422C>T (p.Ala474=) rs727505000
NM_004281.3(BAG3):c.1588G>A (p.Val530Met) rs144678100
NM_004281.3(BAG3):c.1674G>A (p.Ala558=) rs142981190
NM_004281.3(BAG3):c.180+13C>T rs727504938
NM_004281.3(BAG3):c.230C>T (p.Pro77Leu) rs141355480
NM_004281.3(BAG3):c.25A>G (p.Met9Val) rs137965903
NM_004281.3(BAG3):c.463G>A (p.Ala155Thr) rs61756328
NM_004281.3(BAG3):c.465A>G (p.Ala155=) rs775151738
NM_004281.3(BAG3):c.471G>A (p.Ala157=) rs148985314
NM_004281.3(BAG3):c.549C>G (p.Ser183=) rs112929734
NM_004281.3(BAG3):c.645C>T (p.Asn215=) rs138078305
NM_004281.3(BAG3):c.705G>A (p.Ala235=) rs141328836
NM_004281.3(BAG3):c.771C>T (p.Pro257=) rs200212999
NM_004281.3(BAG3):c.781C>T (p.Arg261Trp) rs548032105
NM_004281.3(BAG3):c.870C>G (p.Pro290=) rs140737221
NM_004281.3(BAG3):c.888C>T (p.His296=) rs139399890

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