ClinVar Miner

List of variants in gene BAG3 reported as likely benign for Cardiovascular phenotype

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Total variants: 102
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HGVS dbSNP gnomAD frequency
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.1503C>A (p.Val501=) rs147277075 0.00089
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.855G>A (p.Thr285=) rs147259596 0.00048
NM_004281.4(BAG3):c.888C>T (p.His296=) rs139399890 0.00040
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu) rs143919208 0.00038
NM_004281.4(BAG3):c.230C>T (p.Pro77Leu) rs141355480 0.00033
NM_004281.4(BAG3):c.381A>T (p.Ala127=) rs140594879 0.00030
NM_004281.4(BAG3):c.498C>T (p.His166=) rs111682654 0.00029
NM_004281.4(BAG3):c.771C>T (p.Pro257=) rs200212999 0.00028
NM_004281.4(BAG3):c.898G>A (p.Asp300Asn) rs78439745 0.00026
NM_004281.4(BAG3):c.645C>T (p.Asn215=) rs138078305 0.00025
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.471G>A (p.Ala157=) rs148985314 0.00021
NM_004281.4(BAG3):c.96G>T (p.Pro32=) rs372083121 0.00017
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.1423G>A (p.Asp475Asn) rs138832242 0.00008
NM_004281.4(BAG3):c.211C>T (p.Arg71Trp) rs387906874 0.00008
NM_004281.4(BAG3):c.432C>A (p.Thr144=) rs144928892 0.00008
NM_004281.4(BAG3):c.470C>T (p.Ala157Val) rs541080567 0.00007
NM_004281.4(BAG3):c.636C>T (p.His212=) rs150379892 0.00007
NM_004281.4(BAG3):c.1166G>A (p.Ser389Asn) rs140251789 0.00006
NM_004281.4(BAG3):c.1362C>T (p.Ile454=) rs372417286 0.00006
NM_004281.4(BAG3):c.1422C>T (p.Ala474=) rs727505000 0.00006
NM_004281.4(BAG3):c.400T>A (p.Ser134Thr) rs375257731 0.00006
NM_004281.4(BAG3):c.693G>A (p.Thr231=) rs144034433 0.00006
NM_004281.4(BAG3):c.822G>A (p.Ser274=) rs776700820 0.00005
NM_004281.4(BAG3):c.1446C>T (p.Asp482=) rs767539919 0.00004
NM_004281.4(BAG3):c.1635C>G (p.Pro545=) rs148597097 0.00004
NM_004281.4(BAG3):c.1659A>T (p.Glu553Asp) rs763530097 0.00004
NM_004281.4(BAG3):c.627G>A (p.Pro209=) rs188555685 0.00004
NM_004281.4(BAG3):c.795G>A (p.Pro265=) rs180736121 0.00004
NM_004281.4(BAG3):c.1281C>T (p.Ala427=) rs748724796 0.00003
NM_004281.4(BAG3):c.138C>T (p.Thr46=) rs777267711 0.00003
NM_004281.4(BAG3):c.1563G>A (p.Leu521=) rs1045652182 0.00003
NM_004281.4(BAG3):c.891C>T (p.Thr297=) rs372571986 0.00003
NM_004281.4(BAG3):c.1239C>T (p.Ala413=) rs201137108 0.00002
NM_004281.4(BAG3):c.318G>T (p.Arg106=) rs750075933 0.00002
NM_004281.4(BAG3):c.378G>A (p.Ala126=) rs753235577 0.00002
NM_004281.4(BAG3):c.705G>A (p.Ala235=) rs141328836 0.00002
NM_004281.4(BAG3):c.897C>T (p.Val299=) rs763915884 0.00002
NM_004281.4(BAG3):c.1062G>A (p.Lys354=) rs577392366 0.00001
NM_004281.4(BAG3):c.1266G>C (p.Val422=) rs779661440 0.00001
NM_004281.4(BAG3):c.1299G>A (p.Gln433=) rs374858685 0.00001
NM_004281.4(BAG3):c.1372T>C (p.Leu458=) rs1176479605 0.00001
NM_004281.4(BAG3):c.1593A>G (p.Ala531=) rs1057521271 0.00001
NM_004281.4(BAG3):c.1698A>G (p.Thr566=) rs199837016 0.00001
NM_004281.4(BAG3):c.306C>T (p.Gly102=) rs202006167 0.00001
NM_004281.4(BAG3):c.465A>G (p.Ala155=) rs775151738 0.00001
NM_004281.4(BAG3):c.573C>T (p.Ser191=) rs753386051 0.00001
NM_004281.4(BAG3):c.607C>A (p.Arg203=) rs1047671466 0.00001
NM_004281.4(BAG3):c.786G>A (p.Ala262=) rs775938242 0.00001
NM_004281.4(BAG3):c.828G>A (p.Arg276=) rs752538980 0.00001
NM_004281.4(BAG3):c.1023G>A (p.Val341=)
NM_004281.4(BAG3):c.1029C>G (p.Arg343=)
NM_004281.4(BAG3):c.1125T>C (p.Pro375=) rs1847240164
NM_004281.4(BAG3):c.1140T>C (p.Pro380=)
NM_004281.4(BAG3):c.1152C>T (p.Pro384=) rs2134068948
NM_004281.4(BAG3):c.1155T>C (p.Ser385=) rs750681972
NM_004281.4(BAG3):c.1161C>T (p.Pro387=) rs919491747
NM_004281.4(BAG3):c.1176A>G (p.Thr392=)
NM_004281.4(BAG3):c.1260A>C (p.Pro420=)
NM_004281.4(BAG3):c.1314T>C (p.Ala438=)
NM_004281.4(BAG3):c.1329A>G (p.Glu443=)
NM_004281.4(BAG3):c.132C>T (p.Ser44=) rs2134050640
NM_004281.4(BAG3):c.1401A>G (p.Ser467=) rs1452240685
NM_004281.4(BAG3):c.1428G>A (p.Val476=) rs1589632894
NM_004281.4(BAG3):c.1440G>A (p.Arg480=) rs1199766314
NM_004281.4(BAG3):c.1503C>T (p.Val501=) rs147277075
NM_004281.4(BAG3):c.1530C>T (p.Leu510=)
NM_004281.4(BAG3):c.1541A>G (p.Asn514Ser) rs1564776999
NM_004281.4(BAG3):c.1554T>C (p.Asp518=)
NM_004281.4(BAG3):c.1647C>T (p.Thr549=)
NM_004281.4(BAG3):c.165C>T (p.Pro55=) rs988033291
NM_004281.4(BAG3):c.166T>C (p.Ser56Pro)
NM_004281.4(BAG3):c.168T>C (p.Ser56=)
NM_004281.4(BAG3):c.210C>T (p.Ser70=)
NM_004281.4(BAG3):c.219C>T (p.Gly73=)
NM_004281.4(BAG3):c.255G>T (p.Val85=)
NM_004281.4(BAG3):c.261C>T (p.Pro87=) rs1390921760
NM_004281.4(BAG3):c.387G>A (p.Ala129=) rs764875756
NM_004281.4(BAG3):c.430A>G (p.Thr144Ala)
NM_004281.4(BAG3):c.495C>T (p.Ser165=) rs35261472
NM_004281.4(BAG3):c.519T>A (p.Ser173=)
NM_004281.4(BAG3):c.540A>C (p.Ser180=)
NM_004281.4(BAG3):c.561C>T (p.Ser187=)
NM_004281.4(BAG3):c.606G>A (p.Pro202=) rs74157690
NM_004281.4(BAG3):c.651C>T (p.Thr217=)
NM_004281.4(BAG3):c.75A>C (p.Gly25=)
NM_004281.4(BAG3):c.777C>T (p.Pro259=)
NM_004281.4(BAG3):c.792C>G (p.Ser264=)
NM_004281.4(BAG3):c.834C>G (p.Gly278=) rs2134065380
NM_004281.4(BAG3):c.870C>A (p.Pro290=) rs140737221
NM_004281.4(BAG3):c.981A>G (p.Pro327=) rs1030445553
NM_004281.4(BAG3):c.984T>G (p.Val328=) rs753140913
NM_004281.4(BAG3):c.998C>T (p.Pro333Leu)

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