ClinVar Miner

List of variants in gene BAG3 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 23
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HGVS dbSNP
NM_004281.3(BAG3):c.-4C>T rs727502894
NM_004281.3(BAG3):c.1015A>G (p.Ile339Val) rs757353917
NM_004281.3(BAG3):c.1118G>A (p.Cys373Tyr) rs876657745
NM_004281.3(BAG3):c.1217C>T (p.Thr406Ile) rs727502900
NM_004281.3(BAG3):c.1240G>A (p.Glu414Lys) rs117749531
NM_004281.3(BAG3):c.1274T>A (p.Val425Glu) rs727502901
NM_004281.3(BAG3):c.181-15C>T rs397516882
NM_004281.3(BAG3):c.200A>G (p.Asn67Ser) rs572036022
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.283C>G (p.Pro95Ala) rs727502898
NM_004281.3(BAG3):c.317G>A (p.Arg106Gln)
NM_004281.3(BAG3):c.362G>A (p.Arg121Gln) rs876657746
NM_004281.3(BAG3):c.386C>T (p.Ala129Val) rs876657747
NM_004281.3(BAG3):c.400T>A (p.Ser134Thr) rs375257731
NM_004281.3(BAG3):c.467C>G (p.Ala156Gly) rs572038196
NM_004281.3(BAG3):c.49G>C (p.Gly17Arg) rs727502895
NM_004281.3(BAG3):c.55C>A (p.Arg19Ser) rs727502896
NM_004281.3(BAG3):c.695A>T (p.His232Leu) rs746241240
NM_004281.3(BAG3):c.785C>T (p.Ala262Val) rs397516883
NM_004281.3(BAG3):c.821C>T (p.Ser274Leu) rs143919208
NM_004281.3(BAG3):c.826C>T (p.Arg276Trp) rs759573189
NM_004281.3(BAG3):c.872C>T (p.Ser291Leu) rs368866313
NM_004281.3(BAG3):c.910-10C>G rs727502899

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