ClinVar Miner

List of variants in gene BAG3 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_004281.4(BAG3):c.1296A>G (p.Val432=) rs196295 0.75935
NM_004281.4(BAG3):c.451T>C (p.Cys151Arg) rs2234962 0.14532
NM_004281.4(BAG3):c.1220C>T (p.Pro407Leu) rs3858340 0.12393
NM_004281.4(BAG3):c.1002T>G (p.Pro334=) rs3858339 0.12375
NM_004281.4(BAG3):c.231G>A (p.Pro77=) rs143752613 0.00441
NM_004281.4(BAG3):c.249C>A (p.His83Gln) rs151331972 0.00344
NM_004281.4(BAG3):c.606G>T (p.Pro202=) rs74157690 0.00341
NM_004281.4(BAG3):c.187C>G (p.Pro63Ala) rs144041999 0.00328
NM_004281.4(BAG3):c.1138C>T (p.Pro380Ser) rs144692954 0.00327
NM_004281.4(BAG3):c.181-9T>A rs139232658 0.00317
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr) rs61756328 0.00239
NM_004281.4(BAG3):c.-17G>A rs200388926 0.00218
NM_004281.4(BAG3):c.25A>G (p.Met9Val) rs137965903 0.00175
NM_004281.4(BAG3):c.909+17G>A rs139086861 0.00153
NM_004281.4(BAG3):c.549C>G (p.Ser183=) rs112929734 0.00141
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val) rs34656239 0.00097
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe) rs145393807 0.00085
NM_004281.4(BAG3):c.870C>G (p.Pro290=) rs140737221 0.00055
NM_004281.4(BAG3):c.888C>T (p.His296=) rs139399890 0.00040
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123 0.00036
NM_004281.4(BAG3):c.230C>T (p.Pro77Leu) rs141355480 0.00033
NM_004281.4(BAG3):c.898G>A (p.Asp300Asn) rs78439745 0.00026
NM_004281.4(BAG3):c.1588G>A (p.Val530Met) rs144678100 0.00016
NM_004281.4(BAG3):c.653G>A (p.Arg218Gln) rs201638005 0.00016
NM_004281.4(BAG3):c.1029C>A (p.Arg343=) rs117972572 0.00013
NM_004281.4(BAG3):c.554C>T (p.Ser185Leu) rs730880054 0.00009
NM_004281.4(BAG3):c.211C>T (p.Arg71Trp) rs387906874 0.00008
NM_004281.4(BAG3):c.827G>A (p.Arg276Gln) rs372970842 0.00007
NM_004281.4(BAG3):c.693G>A (p.Thr231=) rs144034433 0.00006
NM_004281.4(BAG3):c.1659A>T (p.Glu553Asp) rs763530097 0.00004
NM_004281.4(BAG3):c.181-15C>T rs397516882 0.00004
NM_004281.4(BAG3):c.191C>T (p.Ser64Phe) rs780615753 0.00004
NM_004281.4(BAG3):c.897C>T (p.Val299=) rs763915884 0.00002
NM_004281.4(BAG3):c.1202C>G (p.Ala401Gly) rs775153939 0.00001
NM_004281.4(BAG3):c.1266G>C (p.Val422=) rs779661440 0.00001
NM_004281.4(BAG3):c.1410C>T (p.Pro470=) rs749034517 0.00001
NM_004281.4(BAG3):c.362G>A (p.Arg121Gln) rs876657746 0.00001
NM_004281.4(BAG3):c.508-17C>T rs1410668640 0.00001
NM_004281.4(BAG3):c.1088A>C (p.Glu363Ala) rs1345725468
NM_004281.4(BAG3):c.1135G>A (p.Gly379Ser) rs886951707
NM_004281.4(BAG3):c.1318G>A (p.Asp440Asn) rs878854652
NM_004281.4(BAG3):c.1496T>A (p.Ile499Asn)
NM_004281.4(BAG3):c.206C>T (p.Pro69Leu)
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.4(BAG3):c.212G>T (p.Arg71Leu) rs35434411
NM_004281.4(BAG3):c.468GGC[4] (p.Ala160dup) rs139438727
NM_004281.4(BAG3):c.533A>G (p.Asp178Gly)

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