ClinVar Miner

List of variants in gene BAG3 studied for Cardiovascular phenotype

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Total variants: 42
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HGVS dbSNP
NM_004281.3(BAG3):c.1002T>G (p.Pro334=) rs3858339
NM_004281.3(BAG3):c.1029C>A (p.Arg343=) rs117972572
NM_004281.3(BAG3):c.1034_1038del (p.Glu345fs) rs1554877731
NM_004281.3(BAG3):c.1138C>T (p.Pro380Ser) rs144692954
NM_004281.3(BAG3):c.1157C>A (p.Ser386Tyr) rs756178548
NM_004281.3(BAG3):c.1220C>T (p.Pro407Leu) rs3858340
NM_004281.3(BAG3):c.1262G>A (p.Gly421Glu) rs886039025
NM_004281.3(BAG3):c.1288G>A (p.Glu430Lys) rs774713887
NM_004281.3(BAG3):c.1292dup (p.Val432fs) rs886039182
NM_004281.3(BAG3):c.1296A>G (p.Val432=) rs196295
NM_004281.3(BAG3):c.1362C>T (p.Ile454=) rs372417286
NM_004281.3(BAG3):c.1411G>A (p.Glu471Lys) rs778496291
NM_004281.3(BAG3):c.1503C>A (p.Val501=) rs147277075
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.1659A>T (p.Glu553Asp) rs763530097
NM_004281.3(BAG3):c.187C>G (p.Pro63Ala) rs144041999
NM_004281.3(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.3(BAG3):c.25A>G (p.Met9Val) rs137965903
NM_004281.3(BAG3):c.262C>T (p.Gln88Ter) rs1554877001
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.367C>T (p.Arg123Ter) rs387906875
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.481C>T (p.Gln161Ter) rs886039044
NM_004281.3(BAG3):c.499G>A (p.Gly167Arg) rs543720798
NM_004281.3(BAG3):c.542C>T (p.Ser181Phe) rs1482925321
NM_004281.3(BAG3):c.549C>G (p.Ser183=) rs112929734
NM_004281.3(BAG3):c.616A>C (p.Ile206Leu) rs199700646
NM_004281.3(BAG3):c.652C>T (p.Arg218Trp) rs397514506
NM_004281.3(BAG3):c.653G>A (p.Arg218Gln) rs201638005
NM_004281.3(BAG3):c.679C>G (p.Gln227Glu) rs149517238
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123
NM_004281.3(BAG3):c.785C>T (p.Ala262Val) rs397516883
NM_004281.3(BAG3):c.795G>A (p.Pro265=) rs180736121
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.892G>A (p.Val298Met) rs150048651
NM_004281.3(BAG3):c.898G>A (p.Asp300Asn) rs78439745
NM_004281.3(BAG3):c.96G>T (p.Pro32=) rs372083121
NM_004281.3(BAG3):c.983T>C (p.Val328Ala) rs765627299

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