ClinVar Miner

List of variants in gene BAG3 reported as uncertain significance for Dilated cardiomyopathy 1HH

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_004281.4(BAG3):c.-284G>C rs192502283 0.01069
NM_004281.4(BAG3):c.-271C>T rs144814361 0.00867
NM_004281.4(BAG3):c.-294A>C rs544280047 0.00385
NM_004281.4(BAG3):c.-293T>A rs557535632 0.00284
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.-95G>A rs111750619 0.00218
NM_004281.4(BAG3):c.*267C>A rs552025009 0.00153
NM_004281.4(BAG3):c.1587C>T (p.Ala529=) rs149358702 0.00144
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.*402T>C rs541591765 0.00068
NM_004281.4(BAG3):c.855G>A (p.Thr285=) rs147259596 0.00048
NM_004281.4(BAG3):c.888C>T (p.His296=) rs139399890 0.00040
NM_004281.4(BAG3):c.-86G>A rs913687992 0.00031
NM_004281.4(BAG3):c.381A>T (p.Ala127=) rs140594879 0.00030
NM_004281.4(BAG3):c.1240G>A (p.Glu414Lys) rs117749531 0.00024
NM_004281.4(BAG3):c.1674G>A (p.Ala558=) rs142981190 0.00021
NM_004281.4(BAG3):c.*399G>T rs774188346 0.00019
NM_004281.4(BAG3):c.1588G>A (p.Val530Met) rs144678100 0.00016
NM_004281.4(BAG3):c.1634C>G (p.Pro545Arg) rs759348679 0.00014
NM_004281.4(BAG3):c.1029C>A (p.Arg343=) rs117972572 0.00013
NM_004281.4(BAG3):c.1321A>G (p.Asn441Asp) rs201181493 0.00011
NM_004281.4(BAG3):c.415C>T (p.Arg139Trp) rs556465096 0.00011
NM_004281.4(BAG3):c.554C>T (p.Ser185Leu) rs730880054 0.00009
NM_004281.4(BAG3):c.616A>C (p.Ile206Leu) rs199700646 0.00009
NM_004281.4(BAG3):c.-128G>T rs543269835 0.00008
NM_004281.4(BAG3):c.-18G>A rs754210695 0.00006
NM_004281.4(BAG3):c.-285C>A rs866276705 0.00006
NM_004281.4(BAG3):c.-4C>T rs727502894 0.00006
NM_004281.4(BAG3):c.1214C>T (p.Ala405Val) rs11199064 0.00006
NM_004281.4(BAG3):c.400T>A (p.Ser134Thr) rs375257731 0.00006
NM_004281.4(BAG3):c.487C>T (p.Pro163Ser) rs746956979 0.00006
NM_004281.4(BAG3):c.693G>A (p.Thr231=) rs144034433 0.00006
NM_004281.4(BAG3):c.181-15C>T rs397516882 0.00004
NM_004281.4(BAG3):c.*199A>C rs950081061 0.00003
NM_004281.4(BAG3):c.-155C>G rs963964101 0.00002
NM_004281.4(BAG3):c.13A>G (p.Thr5Ala) rs777752849 0.00001
NM_004281.4(BAG3):c.1651C>A (p.Gln551Lys) rs577455773 0.00001
NM_004281.4(BAG3):c.337G>A (p.Val113Ile) rs781093275 0.00001
NM_004281.4(BAG3):c.343C>T (p.Pro115Ser) rs774241343 0.00001
NM_004281.4(BAG3):c.465A>G (p.Ala155=) rs775151738 0.00001
NM_004281.4(BAG3):c.836C>T (p.Ser279Leu) rs751261054 0.00001
NM_004281.4(BAG3):c.*319C>T rs148967962
NM_004281.4(BAG3):c.*455G>A rs978995119
NM_004281.4(BAG3):c.*469A>G rs1847262118
NM_004281.4(BAG3):c.-285C>T rs866276705
NM_004281.4(BAG3):c.-2G>T rs1846841562
NM_004281.4(BAG3):c.-319C>T rs987450541
NM_004281.4(BAG3):c.-87G>T rs879223257
NM_004281.4(BAG3):c.1503C>T (p.Val501=) rs147277075
NM_004281.4(BAG3):c.1667C>A (p.Ala556Glu) rs886046756
NM_004281.4(BAG3):c.467C>G (p.Ala156Gly) rs572038196
NM_004281.4(BAG3):c.634C>A (p.His212Asn) rs752772180
NM_004281.4(BAG3):c.637G>A (p.Glu213Lys) rs1311591078
NM_004281.4(BAG3):c.7G>T (p.Ala3Ser) rs956429406

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