ClinVar Miner

List of variants in gene BAG3 reported as likely benign for not specified

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Total variants: 48
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HGVS dbSNP
NM_004281.3(BAG3):c.-18G>A rs754210695
NM_004281.3(BAG3):c.1029C>A (p.Arg343=) rs117972572
NM_004281.3(BAG3):c.105C>G (p.Gly35=) rs1057523771
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.1354C>T (p.Leu452=) rs751439966
NM_004281.3(BAG3):c.1362C>T (p.Ile454=) rs372417286
NM_004281.3(BAG3):c.1410C>T (p.Pro470=) rs749034517
NM_004281.3(BAG3):c.1422C>T (p.Ala474=) rs727505000
NM_004281.3(BAG3):c.1423G>A (p.Asp475Asn) rs138832242
NM_004281.3(BAG3):c.1436C>T (p.Ala479Val) rs34656239
NM_004281.3(BAG3):c.1446C>T (p.Asp482=) rs767539919
NM_004281.3(BAG3):c.1447G>A (p.Gly483Ser) rs570294713
NM_004281.3(BAG3):c.1588G>A (p.Val530Met) rs144678100
NM_004281.3(BAG3):c.1593A>G (p.Ala531=) rs1057521271
NM_004281.3(BAG3):c.1674G>A (p.Ala558=) rs142981190
NM_004281.3(BAG3):c.180+13C>T rs727504938
NM_004281.3(BAG3):c.180+43C>T rs112546447
NM_004281.3(BAG3):c.181-10T>C rs765292614
NM_004281.3(BAG3):c.204C>G (p.Gly68=) rs1057522144
NM_004281.3(BAG3):c.212G>T (p.Arg71Leu) rs35434411
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.264G>A (p.Gln88=) rs779686349
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.381A>T (p.Ala127=) rs140594879
NM_004281.3(BAG3):c.387G>A (p.Ala129=) rs764875756
NM_004281.3(BAG3):c.460G>A (p.Val154Met) rs376198104
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.480C>T (p.Ala160=) rs749405417
NM_004281.3(BAG3):c.498C>T (p.His166=) rs111682654
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.653G>A (p.Arg218Gln) rs201638005
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.802T>C (p.Ser268Pro) rs761965592
NM_004281.3(BAG3):c.822G>A (p.Ser274=) rs776700820
NM_004281.3(BAG3):c.870C>A (p.Pro290=) rs140737221
NM_004281.3(BAG3):c.870C>G (p.Pro290=) rs140737221
NM_004281.3(BAG3):c.888C>T (p.His296=) rs139399890
NM_004281.3(BAG3):c.891C>T (p.Thr297=) rs372571986
NM_004281.3(BAG3):c.897C>T (p.Val299=) rs763915884
NM_004281.3(BAG3):c.898G>A (p.Asp300Asn) rs78439745

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