ClinVar Miner

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

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Total variants: 40
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HGVS dbSNP
NM_004281.3(BAG3):c.-4C>T rs727502894
NM_004281.3(BAG3):c.1028G>C (p.Arg343Pro) rs774085746
NM_004281.3(BAG3):c.1035G>C (p.Glu345Asp) rs1057522401
NM_004281.3(BAG3):c.1100C>G (p.Pro367Arg) rs786205347
NM_004281.3(BAG3):c.115_117delTTC (p.Phe39del) rs1064796808
NM_004281.3(BAG3):c.1166G>A (p.Ser389Asn) rs140251789
NM_004281.3(BAG3):c.1172C>T (p.Ala391Val) rs200242752
NM_004281.3(BAG3):c.1201G>A (p.Ala401Thr) rs1064796532
NM_004281.3(BAG3):c.1232_1234delGAG (p.Gly411del) rs761727804
NM_004281.3(BAG3):c.13A>G (p.Thr5Ala) rs777752849
NM_004281.3(BAG3):c.142A>C (p.Thr48Pro) rs794728980
NM_004281.3(BAG3):c.1630G>A (p.Asp544Asn) rs786205466
NM_004281.3(BAG3):c.1634C>G (p.Pro545Arg) rs759348679
NM_004281.3(BAG3):c.1639A>C (p.Thr547Pro) rs1057523768
NM_004281.3(BAG3):c.191C>T (p.Ser64Phe) rs780615753
NM_004281.3(BAG3):c.320A>C (p.Gln107Pro) rs760437650
NM_004281.3(BAG3):c.415C>T (p.Arg139Trp) rs556465096
NM_004281.3(BAG3):c.418G>A (p.Gly140Ser) rs780169403
NM_004281.3(BAG3):c.460G>C (p.Val154Leu) rs376198104
NM_004281.3(BAG3):c.509G>A (p.Arg170Gln) rs140904592
NM_004281.3(BAG3):c.512C>T (p.Ser171Phe) rs794728978
NM_004281.3(BAG3):c.569C>T (p.Ser190Phe) rs1057523462
NM_004281.3(BAG3):c.608G>A (p.Arg203Gln) rs1057524225
NM_004281.3(BAG3):c.616A>C (p.Ile206Leu) rs199700646
NM_004281.3(BAG3):c.653G>A (p.Arg218Gln) rs201638005
NM_004281.3(BAG3):c.677A>G (p.His226Arg) rs1554877252
NM_004281.3(BAG3):c.679C>G (p.Gln227Glu) rs149517238
NM_004281.3(BAG3):c.67C>T (p.Pro23Ser) rs747846089
NM_004281.3(BAG3):c.743A>G (p.His248Arg) rs369947845
NM_004281.3(BAG3):c.784G>A (p.Ala262Thr) rs876661343
NM_004281.3(BAG3):c.788C>T (p.Ala263Val) rs1057523599
NM_004281.3(BAG3):c.821C>T (p.Ser274Leu) rs143919208
NM_004281.3(BAG3):c.836C>T (p.Ser279Leu) rs751261054
NM_004281.3(BAG3):c.880C>A (p.Arg294Ser) rs144585878
NM_004281.3(BAG3):c.881G>A (p.Arg294His) rs151335530
NM_004281.3(BAG3):c.889A>G (p.Thr297Ala) rs794728979
NM_004281.3(BAG3):c.909G>C (p.Gln303His) rs1554877302
NM_004281.3(BAG3):c.943T>A (p.Ser315Thr) rs761417402
NM_004281.3(BAG3):c.961C>T (p.Pro321Ser) rs376832654
NM_004281.3(BAG3):c.997C>T (p.Pro333Ser) rs1393181351

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