ClinVar Miner

List of variants in gene BAG3 studied for Dilated Cardiomyopathy, Dominant

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Total variants: 49
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HGVS dbSNP
NM_004281.3(BAG3):c.*218G>C rs8946
NM_004281.3(BAG3):c.*243_*245delGTT rs3981124
NM_004281.3(BAG3):c.*267C>A rs552025009
NM_004281.3(BAG3):c.*306_*307delTT rs796515184
NM_004281.3(BAG3):c.*319C>T rs148967962
NM_004281.3(BAG3):c.*31C>T rs116329258
NM_004281.3(BAG3):c.*399G>T rs774188346
NM_004281.3(BAG3):c.*402T>C rs541591765
NM_004281.3(BAG3):c.*535A>G rs11199065
NM_004281.3(BAG3):c.-17G>A rs200388926
NM_004281.3(BAG3):c.-271C>T rs144814361
NM_004281.3(BAG3):c.-284G>C rs192502283
NM_004281.3(BAG3):c.-285C>A rs866276705
NM_004281.3(BAG3):c.-285C>T rs866276705
NM_004281.3(BAG3):c.-293T>A rs557535632
NM_004281.3(BAG3):c.-294A>C rs544280047
NM_004281.3(BAG3):c.-87G>T rs879223257
NM_004281.3(BAG3):c.-95G>A rs111750619
NM_004281.3(BAG3):c.1002T>G (p.Pro334=) rs3858339
NM_004281.3(BAG3):c.1214C>T (p.Ala405Val) rs11199064
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.1296A>G (p.Val432=) rs196295
NM_004281.3(BAG3):c.1298A>G (p.Gln433Arg) rs886046755
NM_004281.3(BAG3):c.1436C>T (p.Ala479Val) rs34656239
NM_004281.3(BAG3):c.1503C>T (p.Val501=) rs147277075
NM_004281.3(BAG3):c.1571T>C (p.Ile524Thr) rs752390475
NM_004281.3(BAG3):c.1588G>A (p.Val530Met) rs144678100
NM_004281.3(BAG3):c.1634C>G (p.Pro545Arg) rs759348679
NM_004281.3(BAG3):c.1667C>A (p.Ala556Glu) rs886046756
NM_004281.3(BAG3):c.1674G>A (p.Ala558=) rs142981190
NM_004281.3(BAG3):c.181-15C>T rs397516882
NM_004281.3(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.3(BAG3):c.231G>A (p.Pro77=) rs143752613
NM_004281.3(BAG3):c.381A>T (p.Ala127=) rs140594879
NM_004281.3(BAG3):c.415C>T (p.Arg139Trp) rs556465096
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.549C>G (p.Ser183=) rs112929734
NM_004281.3(BAG3):c.554C>T (p.Ser185Leu) rs730880054
NM_004281.3(BAG3):c.564G>T (p.Leu188=) rs886046754
NM_004281.3(BAG3):c.606G>T (p.Pro202=) rs74157690
NM_004281.3(BAG3):c.693G>A (p.Thr231=) rs144034433
NM_004281.3(BAG3):c.855G>A (p.Thr285=) rs147259596
NM_004281.3(BAG3):c.888C>T (p.His296=) rs139399890
NM_004281.3(BAG3):c.898G>A (p.Asp300Asn) rs78439745

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