ClinVar Miner

List of variants in gene BAG3 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 148
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004281.4(BAG3):c.249C>A (p.His83Gln) rs151331972 0.00344
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe) rs145393807 0.00085
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu) rs143919208 0.00038
NM_004281.4(BAG3):c.771C>T (p.Pro257=) rs200212999 0.00028
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.1634C>G (p.Pro545Arg) rs759348679 0.00014
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.508C>T (p.Arg170Trp) rs200479768 0.00011
NM_004281.4(BAG3):c.554C>T (p.Ser185Leu) rs730880054 0.00009
NM_004281.4(BAG3):c.605C>T (p.Pro202Leu) rs556000090 0.00009
NM_004281.4(BAG3):c.616A>C (p.Ile206Leu) rs199700646 0.00009
NM_004281.4(BAG3):c.211C>T (p.Arg71Trp) rs387906874 0.00008
NM_004281.4(BAG3):c.892G>A (p.Val298Met) rs150048651 0.00007
NM_004281.4(BAG3):c.1166G>A (p.Ser389Asn) rs140251789 0.00006
NM_004281.4(BAG3):c.1214C>T (p.Ala405Val) rs11199064 0.00006
NM_004281.4(BAG3):c.1523A>G (p.Tyr508Cys) rs747583925 0.00006
NM_004281.4(BAG3):c.167C>G (p.Ser56Cys) rs777100532 0.00006
NM_004281.4(BAG3):c.487C>T (p.Pro163Ser) rs746956979 0.00006
NM_004281.4(BAG3):c.574G>A (p.Gly192Ser) rs201487919 0.00006
NM_004281.4(BAG3):c.785C>T (p.Ala262Val) rs397516883 0.00006
NM_004281.4(BAG3):c.133C>T (p.Arg45Cys) rs747820097 0.00005
NM_004281.4(BAG3):c.872C>T (p.Ser291Leu) rs368866313 0.00005
NM_004281.4(BAG3):c.1291A>G (p.Lys431Glu) rs1374652846 0.00004
NM_004281.4(BAG3):c.1625C>T (p.Ala542Val) rs770920565 0.00004
NM_004281.4(BAG3):c.191C>T (p.Ser64Phe) rs780615753 0.00004
NM_004281.4(BAG3):c.316C>T (p.Arg106Trp) rs767341152 0.00004
NM_004281.4(BAG3):c.34G>A (p.Val12Met) rs367917821 0.00004
NM_004281.4(BAG3):c.652C>T (p.Arg218Trp) rs397514506 0.00004
NM_004281.4(BAG3):c.743A>G (p.His248Arg) rs369947845 0.00004
NM_004281.4(BAG3):c.968G>A (p.Ser323Asn) rs754387872 0.00004
NM_004281.4(BAG3):c.1028G>C (p.Arg343Pro) rs774085746 0.00003
NM_004281.4(BAG3):c.1312G>T (p.Ala438Ser) rs1031608025 0.00003
NM_004281.4(BAG3):c.509G>A (p.Arg170Gln) rs140904592 0.00003
NM_004281.4(BAG3):c.854C>T (p.Thr285Met) rs375650805 0.00003
NM_004281.4(BAG3):c.961C>T (p.Pro321Ser) rs376832654 0.00003
NM_004281.4(BAG3):c.1150C>T (p.Pro384Ser) rs1286082290 0.00002
NM_004281.4(BAG3):c.1411G>A (p.Glu471Lys) rs778496291 0.00002
NM_004281.4(BAG3):c.1558C>T (p.Pro520Ser) rs760699965 0.00002
NM_004281.4(BAG3):c.1673C>T (p.Ala558Val) rs185537639 0.00002
NM_004281.4(BAG3):c.320A>C (p.Gln107Pro) rs760437650 0.00002
NM_004281.4(BAG3):c.386C>T (p.Ala129Val) rs876657747 0.00002
NM_004281.4(BAG3):c.494C>T (p.Ser165Phe) rs143756613 0.00002
NM_004281.4(BAG3):c.698A>G (p.Tyr233Cys) rs1415830597 0.00002
NM_004281.4(BAG3):c.715G>A (p.Glu239Lys) rs148544471 0.00002
NM_004281.4(BAG3):c.943T>A (p.Ser315Thr) rs761417402 0.00002
NM_004281.4(BAG3):c.983T>C (p.Val328Ala) rs765627299 0.00002
NM_004281.4(BAG3):c.1027C>T (p.Arg343Cys) rs768613403 0.00001
NM_004281.4(BAG3):c.1035G>C (p.Glu345Asp) rs1057522401 0.00001
NM_004281.4(BAG3):c.109C>T (p.Pro37Ser) rs764177199 0.00001
NM_004281.4(BAG3):c.1100C>G (p.Pro367Arg) rs786205347 0.00001
NM_004281.4(BAG3):c.1118G>A (p.Cys373Tyr) rs876657745 0.00001
NM_004281.4(BAG3):c.1447G>A (p.Gly483Ser) rs570294713 0.00001
NM_004281.4(BAG3):c.1570A>G (p.Ile524Val) rs764925485 0.00001
NM_004281.4(BAG3):c.1571T>C (p.Ile524Thr) rs752390475 0.00001
NM_004281.4(BAG3):c.1624G>T (p.Ala542Ser) rs760485616 0.00001
NM_004281.4(BAG3):c.1628_1633del (p.Glu543_Pro545delinsAla) rs1847251591 0.00001
NM_004281.4(BAG3):c.1637A>T (p.His546Leu) rs1334550097 0.00001
NM_004281.4(BAG3):c.1639A>C (p.Thr547Pro) rs1057523768 0.00001
NM_004281.4(BAG3):c.164C>T (p.Pro55Leu) rs1277623691 0.00001
NM_004281.4(BAG3):c.1720G>T (p.Ala574Ser) rs779083262 0.00001
NM_004281.4(BAG3):c.1724C>T (p.Pro575Leu) rs748233260 0.00001
NM_004281.4(BAG3):c.341A>G (p.Tyr114Cys) rs769813479 0.00001
NM_004281.4(BAG3):c.368G>A (p.Arg123Gln) rs199991063 0.00001
NM_004281.4(BAG3):c.418G>A (p.Gly140Ser) rs780169403 0.00001
NM_004281.4(BAG3):c.452G>A (p.Cys151Tyr) rs770678896 0.00001
NM_004281.4(BAG3):c.460G>C (p.Val154Leu) rs376198104 0.00001
NM_004281.4(BAG3):c.465A>G (p.Ala155=) rs775151738 0.00001
NM_004281.4(BAG3):c.46A>G (p.Asn16Asp) rs1474784659 0.00001
NM_004281.4(BAG3):c.542C>T (p.Ser181Phe) rs1482925321 0.00001
NM_004281.4(BAG3):c.557C>T (p.Ala186Val) rs766766600 0.00001
NM_004281.4(BAG3):c.67C>T (p.Pro23Ser) rs747846089 0.00001
NM_004281.4(BAG3):c.794C>T (p.Pro265Leu) rs769034041 0.00001
NM_004281.4(BAG3):c.826C>T (p.Arg276Trp) rs759573189 0.00001
NM_004281.4(BAG3):c.836C>T (p.Ser279Leu) rs751261054 0.00001
NM_004281.4(BAG3):c.881G>A (p.Arg294His) rs151335530 0.00001
NM_004281.4(BAG3):c.957C>G (p.Asn319Lys) rs767223665 0.00001
NM_004281.4(BAG3):c.988C>T (p.Pro330Ser) rs762376423 0.00001
NM_004281.4(BAG3):c.997C>T (p.Pro333Ser) rs1393181351 0.00001
NM_004281.4(BAG3):c.1028G>A (p.Arg343His) rs774085746
NM_004281.4(BAG3):c.1028G>T (p.Arg343Leu) rs774085746
NM_004281.4(BAG3):c.1088A>C (p.Glu363Ala) rs1345725468
NM_004281.4(BAG3):c.1114C>T (p.Pro372Ser)
NM_004281.4(BAG3):c.1126C>T (p.Pro376Ser) rs1180366101
NM_004281.4(BAG3):c.112TTC[1] (p.Phe39del) rs1064796808
NM_004281.4(BAG3):c.1165A>G (p.Ser389Gly)
NM_004281.4(BAG3):c.1169T>G (p.Val390Gly)
NM_004281.4(BAG3):c.1172C>T (p.Ala391Val) rs200242752
NM_004281.4(BAG3):c.1201G>A (p.Ala401Thr) rs1064796532
NM_004281.4(BAG3):c.1210G>A (p.Glu404Lys) rs1165453591
NM_004281.4(BAG3):c.1223C>T (p.Pro408Leu)
NM_004281.4(BAG3):c.1232_1234del (p.Gly411del) rs761727804
NM_004281.4(BAG3):c.1255C>T (p.His419Tyr)
NM_004281.4(BAG3):c.1264G>C (p.Val422Leu)
NM_004281.4(BAG3):c.142A>C (p.Thr48Pro) rs794728980
NM_004281.4(BAG3):c.1499A>T (p.Asp500Val) rs2134069399
NM_004281.4(BAG3):c.1504C>G (p.Pro502Ala) rs1564776954
NM_004281.4(BAG3):c.1516C>G (p.Gln506Glu)
NM_004281.4(BAG3):c.1541A>G (p.Asn514Ser) rs1564776999
NM_004281.4(BAG3):c.1564C>T (p.Gln522Ter)
NM_004281.4(BAG3):c.1600A>G (p.Lys534Glu)
NM_004281.4(BAG3):c.1630G>A (p.Asp544Asn) rs786205466
NM_004281.4(BAG3):c.1630G>C (p.Asp544His) rs786205466
NM_004281.4(BAG3):c.1649A>G (p.Gln550Arg) rs2134069541
NM_004281.4(BAG3):c.1663_1666dup (p.Ala556fs) rs1273311196
NM_004281.4(BAG3):c.1667C>A (p.Ala556Glu) rs886046756
NM_004281.4(BAG3):c.1702A>T (p.Thr568Ser)
NM_004281.4(BAG3):c.173G>T (p.Gly58Val) rs138785335
NM_004281.4(BAG3):c.277T>C (p.Tyr93His) rs960439911
NM_004281.4(BAG3):c.280A>G (p.Ile94Val)
NM_004281.4(BAG3):c.293T>G (p.Val98Gly)
NM_004281.4(BAG3):c.2T>G (p.Met1Arg) rs1846841605
NM_004281.4(BAG3):c.322G>T (p.Val108Leu) rs730880053
NM_004281.4(BAG3):c.329C>T (p.Pro110Leu) rs749587347
NM_004281.4(BAG3):c.355A>G (p.Met119Val) rs1334163509
NM_004281.4(BAG3):c.427G>A (p.Glu143Lys)
NM_004281.4(BAG3):c.451_452inv (p.Cys151His)
NM_004281.4(BAG3):c.467C>G (p.Ala156Gly) rs572038196
NM_004281.4(BAG3):c.482A>G (p.Gln161Arg)
NM_004281.4(BAG3):c.499G>A (p.Gly167Arg) rs543720798
NM_004281.4(BAG3):c.49G>C (p.Gly17Arg) rs727502895
NM_004281.4(BAG3):c.512C>T (p.Ser171Phe) rs794728978
NM_004281.4(BAG3):c.520C>T (p.Pro174Ser) rs1472073020
NM_004281.4(BAG3):c.523G>C (p.Ala175Pro)
NM_004281.4(BAG3):c.52G>A (p.Asp18Asn)
NM_004281.4(BAG3):c.534C>G (p.Asp178Glu) rs1847160690
NM_004281.4(BAG3):c.537C>G (p.Cys179Trp) rs1564774433
NM_004281.4(BAG3):c.545C>T (p.Ser182Leu) rs1428247151
NM_004281.4(BAG3):c.549CTC[1] (p.Ser185del) rs763170019
NM_004281.4(BAG3):c.569C>T (p.Ser190Phe) rs1057523462
NM_004281.4(BAG3):c.574G>T (p.Gly192Cys) rs201487919
NM_004281.4(BAG3):c.608G>A (p.Arg203Gln) rs1057524225
NM_004281.4(BAG3):c.616A>G (p.Ile206Val) rs199700646
NM_004281.4(BAG3):c.646G>T (p.Val216Phe) rs148282376
NM_004281.4(BAG3):c.677A>G (p.His226Arg) rs1554877252
NM_004281.4(BAG3):c.724A>G (p.Thr242Ala)
NM_004281.4(BAG3):c.782G>C (p.Arg261Pro) rs746454994
NM_004281.4(BAG3):c.784G>A (p.Ala262Thr) rs876661343
NM_004281.4(BAG3):c.787G>A (p.Ala263Thr)
NM_004281.4(BAG3):c.788C>T (p.Ala263Val) rs1057523599
NM_004281.4(BAG3):c.830A>T (p.Glu277Val) rs762471704
NM_004281.4(BAG3):c.880C>A (p.Arg294Ser) rs144585878
NM_004281.4(BAG3):c.889A>G (p.Thr297Ala) rs794728979
NM_004281.4(BAG3):c.896T>A (p.Val299Asp) rs1489316347
NM_004281.4(BAG3):c.909G>C (p.Gln303His) rs1554877302
NM_004281.4(BAG3):c.925C>G (p.Arg309Gly) rs869248137
NM_004281.4(BAG3):c.95C>T (p.Pro32Leu)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.