List of variants in gene BAG3 reported by Blueprint Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.554C>T (p.Ser185Leu)	rs730880054	0.00009
NM_004281.4(BAG3):c.785C>T (p.Ala262Val)	rs397516883	0.00006
NM_004281.4(BAG3):c.668C>G (p.Pro223Arg)	rs754615028	0.00002
NM_004281.4(BAG3):c.1118G>A (p.Cys373Tyr)	rs876657745	0.00001
NM_004281.4(BAG3):c.322G>A (p.Val108Met)	rs730880053	0.00001
NM_004281.4(BAG3):c.341A>G (p.Tyr114Cys)	rs769813479	0.00001
NM_004281.4(BAG3):c.55C>T (p.Arg19Cys)	rs727502896	0.00001
NM_004281.4(BAG3):c.1297C>T (p.Gln433Ter)	rs730880055
NM_004281.4(BAG3):c.1363G>A (p.Glu455Lys)	rs397516881
NM_004281.4(BAG3):c.1504C>G (p.Pro502Ala)	rs1564776954
NM_004281.4(BAG3):c.284C>T (p.Pro95Leu)	rs869025364
NM_004281.4(BAG3):c.339del (p.Tyr114fs)	rs1589628864
NM_004281.4(BAG3):c.545C>T (p.Ser182Leu)	rs1428247151
NM_004281.4(BAG3):c.909+1G>A	rs869025365

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