List of variants in gene BAG3 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.367C>T (p.Arg123Ter)	rs387906875	0.00001
NM_004281.4(BAG3):c.1257dup (p.Pro420fs)	rs2134069115
NM_004281.4(BAG3):c.1267_1276del (p.Leu423fs)	rs794728981
NM_004281.4(BAG3):c.1363G>A (p.Glu455Lys)	rs397516881
NM_004281.4(BAG3):c.206dup (p.Ser70fs)	rs1554876984
NM_004281.4(BAG3):c.258C>A (p.Tyr86Ter)
NM_004281.4(BAG3):c.268C>T (p.Arg90Ter)	rs1057517945
NM_004281.4(BAG3):c.447dup (p.Gln150fs)
NM_004281.4(BAG3):c.625C>T (p.Pro209Ser)	rs1589630141
NM_004281.4(BAG3):c.626C>T (p.Pro209Leu)	rs121918312
NM_004281.4(BAG3):c.699C>A (p.Tyr233Ter)	rs876661342
NM_004281.4(BAG3):c.709C>T (p.Gln237Ter)	rs2134065221
NM_004281.4(BAG3):c.715G>T (p.Glu239Ter)	rs148544471
NM_004281.4(BAG3):c.72del (p.Gly25fs)	rs727502897
NM_004281.4(BAG3):c.77G>A (p.Trp26Ter)	rs1554875409
NM_004281.4(BAG3):c.889_890del (p.Thr297fs)	rs1847169064
NM_004281.4(BAG3):c.925C>T (p.Arg309Ter)	rs869248137

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