ClinVar Miner

List of variants in gene BAG3 reported as likely benign for Myofibrillar myopathy, BAG3-related; Dilated cardiomyopathy 1HH

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Total variants: 26
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HGVS dbSNP
NM_004281.3(BAG3):c.1029C>A (p.Arg343=) rs117972572
NM_004281.3(BAG3):c.1083G>A (p.Lys361=) rs1060504722
NM_004281.3(BAG3):c.1140T>G (p.Pro380=) rs201449869
NM_004281.3(BAG3):c.1410C>T (p.Pro470=) rs749034517
NM_004281.3(BAG3):c.1425T>C (p.Asp475=) rs376404396
NM_004281.3(BAG3):c.1436C>T (p.Ala479Val) rs34656239
NM_004281.3(BAG3):c.1446C>T (p.Asp482=) rs767539919
NM_004281.3(BAG3):c.1527A>G (p.Glu509=) rs1554877837
NM_004281.3(BAG3):c.1725G>A (p.Pro575=) rs772087416
NM_004281.3(BAG3):c.180+10G>C rs1060504721
NM_004281.3(BAG3):c.280A>T (p.Ile94Phe) rs145393807
NM_004281.3(BAG3):c.339C>T (p.Val113=) rs367861849
NM_004281.3(BAG3):c.372T>G (p.Thr124=) rs766084373
NM_004281.3(BAG3):c.381A>T (p.Ala127=) rs140594879
NM_004281.3(BAG3):c.400T>A (p.Ser134Thr) rs375257731
NM_004281.3(BAG3):c.465A>G (p.Ala155=) rs775151738
NM_004281.3(BAG3):c.471G>A (p.Ala157=) rs148985314
NM_004281.3(BAG3):c.627G>C (p.Pro209=) rs188555685
NM_004281.3(BAG3):c.636C>T (p.His212=) rs150379892
NM_004281.3(BAG3):c.693G>A (p.Thr231=) rs144034433
NM_004281.3(BAG3):c.771C>T (p.Pro257=) rs200212999
NM_004281.3(BAG3):c.819A>G (p.Ala273=) rs1554877282
NM_004281.3(BAG3):c.821C>T (p.Ser274Leu) rs143919208
NM_004281.3(BAG3):c.822G>A (p.Ser274=) rs776700820
NM_004281.3(BAG3):c.855G>A (p.Thr285=) rs147259596
NM_004281.3(BAG3):c.96G>T (p.Pro32=) rs372083121

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