ClinVar Miner

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

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Total variants: 65
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HGVS dbSNP
NM_004281.3(BAG3):c.-4C>T rs727502894
NM_004281.3(BAG3):c.1002T>G (p.Pro334=) rs3858339
NM_004281.3(BAG3):c.100_107del (p.Thr34fs) rs727505283
NM_004281.3(BAG3):c.1015A>G (p.Ile339Val) rs757353917
NM_004281.3(BAG3):c.1067del (p.Pro356fs) rs727505109
NM_004281.3(BAG3):c.1118G>A (p.Cys373Tyr) rs876657745
NM_004281.3(BAG3):c.111C>T (p.Pro37=) rs397516880
NM_004281.3(BAG3):c.1138C>T (p.Pro380Ser) rs144692954
NM_004281.3(BAG3):c.114C>T (p.Phe38=) rs727504929
NM_004281.3(BAG3):c.1217C>T (p.Thr406Ile) rs727502900
NM_004281.3(BAG3):c.1220C>T (p.Pro407Leu) rs3858340
NM_004281.3(BAG3):c.1240G>A (p.Glu414Lys) rs117749531
NM_004281.3(BAG3):c.1274T>A (p.Val425Glu) rs727502901
NM_004281.3(BAG3):c.1296A>G (p.Val432=) rs196295
NM_004281.3(BAG3):c.1344C>T (p.Asp448=) rs727504796
NM_004281.3(BAG3):c.1363G>A (p.Glu455Lys) rs397516881
NM_004281.3(BAG3):c.1422C>T (p.Ala474=) rs727505000
NM_004281.3(BAG3):c.1587C>T (p.Ala529=) rs149358702
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.181-15C>T rs397516882
NM_004281.3(BAG3):c.181-9T>A rs139232658
NM_004281.3(BAG3):c.187C>G (p.Pro63Ala) rs144041999
NM_004281.3(BAG3):c.200A>G (p.Asn67Ser) rs572036022
NM_004281.3(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.3(BAG3):c.230C>T (p.Pro77Leu) rs141355480
NM_004281.3(BAG3):c.231G>A (p.Pro77=) rs143752613
NM_004281.3(BAG3):c.249C>A (p.His83Gln) rs151331972
NM_004281.3(BAG3):c.25A>G (p.Met9Val) rs137965903
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.283C>G (p.Pro95Ala) rs727502898
NM_004281.3(BAG3):c.317G>A (p.Arg106Gln)
NM_004281.3(BAG3):c.362G>A (p.Arg121Gln) rs876657746
NM_004281.3(BAG3):c.367C>T (p.Arg123Ter) rs387906875
NM_004281.3(BAG3):c.386C>T (p.Ala129Val) rs876657747
NM_004281.3(BAG3):c.400T>A (p.Ser134Thr) rs375257731
NM_004281.3(BAG3):c.451T>C (p.Cys151Arg) rs2234962
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.467C>G (p.Ala156Gly) rs572038196
NM_004281.3(BAG3):c.468_470GGC[4] (p.Ala160dup) rs139438727
NM_004281.3(BAG3):c.471G>A (p.Ala157=) rs148985314
NM_004281.3(BAG3):c.49G>C (p.Gly17Arg) rs727502895
NM_004281.3(BAG3):c.549C>G (p.Ser183=) rs112929734
NM_004281.3(BAG3):c.55C>A (p.Arg19Ser) rs727502896
NM_004281.3(BAG3):c.606G>T (p.Pro202=) rs74157690
NM_004281.3(BAG3):c.645C>T (p.Asn215=) rs138078305
NM_004281.3(BAG3):c.653G>A (p.Arg218Gln) rs201638005
NM_004281.3(BAG3):c.695A>T (p.His232Leu) rs746241240
NM_004281.3(BAG3):c.705G>A (p.Ala235=) rs141328836
NM_004281.3(BAG3):c.72del (p.Gly25fs) rs727502897
NM_004281.3(BAG3):c.730C>T (p.Gln244Ter) rs876657634
NM_004281.3(BAG3):c.771C>T (p.Pro257=) rs200212999
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123
NM_004281.3(BAG3):c.77G>A (p.Trp26Ter) rs1554875409
NM_004281.3(BAG3):c.781C>T (p.Arg261Trp) rs548032105
NM_004281.3(BAG3):c.785C>T (p.Ala262Val) rs397516883
NM_004281.3(BAG3):c.821C>T (p.Ser274Leu) rs143919208
NM_004281.3(BAG3):c.826C>T (p.Arg276Trp) rs759573189
NM_004281.3(BAG3):c.870C>G (p.Pro290=) rs140737221
NM_004281.3(BAG3):c.872C>T (p.Ser291Leu) rs368866313
NM_004281.3(BAG3):c.888C>T (p.His296=) rs139399890
NM_004281.3(BAG3):c.910-10C>G rs727502899
NM_004281.3(BAG3):c.925C>T (p.Arg309Ter) rs869248137

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