ClinVar Miner

List of variants in gene BAG3 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_004281.4(BAG3):c.1588G>A (p.Val530Met) rs144678100 0.00016
NM_004281.4(BAG3):c.616A>C (p.Ile206Leu) rs199700646 0.00009
NM_004281.4(BAG3):c.1166G>A (p.Ser389Asn) rs140251789 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.133C>T (p.Arg45Cys) rs747820097 0.00005
NM_004281.4(BAG3):c.1291A>G (p.Lys431Glu) rs1374652846 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.743A>G (p.His248Arg) rs369947845 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.961C>T (p.Pro321Ser) rs376832654 0.00003
NM_004281.4(BAG3):c.1558C>T (p.Pro520Ser) rs760699965 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.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.13A>G (p.Thr5Ala) rs777752849 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.1639A>C (p.Thr547Pro) rs1057523768 0.00001
NM_004281.4(BAG3):c.164C>T (p.Pro55Leu) rs1277623691 0.00001
NM_004281.4(BAG3):c.418G>A (p.Gly140Ser) rs780169403 0.00001
NM_004281.4(BAG3):c.460G>C (p.Val154Leu) rs376198104 0.00001
NM_004281.4(BAG3):c.557C>T (p.Ala186Val) rs766766600 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.997C>T (p.Pro333Ser) rs1393181351 0.00001
NM_004281.4(BAG3):c.1028G>A (p.Arg343His) rs774085746
NM_004281.4(BAG3):c.112TTC[1] (p.Phe39del) rs1064796808
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.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.1541A>G (p.Asn514Ser) rs1564776999
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.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.293T>G (p.Val98Gly)
NM_004281.4(BAG3):c.329C>T (p.Pro110Leu) rs749587347
NM_004281.4(BAG3):c.451_452inv (p.Cys151His)
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.534C>G (p.Asp178Glu) rs1847160690
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.608G>A (p.Arg203Gln) rs1057524225
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.788C>T (p.Ala263Val) rs1057523599
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.909G>C (p.Gln303His) rs1554877302
NM_004281.4(BAG3):c.925C>G (p.Arg309Gly) rs869248137

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