List of variants in gene BAG3 reported as uncertain significance for not specified

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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: 37

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val)	rs34656239	0.00097
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe)	rs145393807	0.00085
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu)	rs143919208	0.00038
NM_004281.4(BAG3):c.1240G>A (p.Glu414Lys)	rs117749531	0.00024
NM_004281.4(BAG3):c.-4C>T	rs727502894	0.00006
NM_004281.4(BAG3):c.400T>A (p.Ser134Thr)	rs375257731	0.00006
NM_004281.4(BAG3):c.785C>T (p.Ala262Val)	rs397516883	0.00006
NM_004281.4(BAG3):c.872C>T (p.Ser291Leu)	rs368866313	0.00005
NM_004281.4(BAG3):c.1291A>G (p.Lys431Glu)	rs1374652846	0.00004
NM_004281.4(BAG3):c.181-15C>T	rs397516882	0.00004
NM_004281.4(BAG3):c.191C>T (p.Ser64Phe)	rs780615753	0.00004
NM_004281.4(BAG3):c.961C>T (p.Pro321Ser)	rs376832654	0.00003
NM_004281.4(BAG3):c.386C>T (p.Ala129Val)	rs876657747	0.00002
NM_004281.4(BAG3):c.1118G>A (p.Cys373Tyr)	rs876657745	0.00001
NM_004281.4(BAG3):c.1202C>G (p.Ala401Gly)	rs775153939	0.00001
NM_004281.4(BAG3):c.1217C>T (p.Thr406Ile)	rs727502900	0.00001
NM_004281.4(BAG3):c.13A>G (p.Thr5Ala)	rs777752849	0.00001
NM_004281.4(BAG3):c.283C>G (p.Pro95Ala)	rs727502898	0.00001
NM_004281.4(BAG3):c.362G>A (p.Arg121Gln)	rs876657746	0.00001
NM_004281.4(BAG3):c.826C>T (p.Arg276Trp)	rs759573189	0.00001
NM_004281.4(BAG3):c.947A>G (p.Gln316Arg)	rs1246603543	0.00001
NM_004281.4(BAG3):c.1015A>G (p.Ile339Val)	rs757353917
NM_004281.4(BAG3):c.1088A>C (p.Glu363Ala)	rs1345725468
NM_004281.4(BAG3):c.1135G>A (p.Gly379Ser)	rs886951707
NM_004281.4(BAG3):c.1274T>A (p.Val425Glu)	rs727502901
NM_004281.4(BAG3):c.1318G>A (p.Asp440Asn)	rs878854652
NM_004281.4(BAG3):c.1496T>A (p.Ile499Asn)
NM_004281.4(BAG3):c.200A>G (p.Asn67Ser)	rs572036022
NM_004281.4(BAG3):c.206C>T (p.Pro69Leu)
NM_004281.4(BAG3):c.317G>A (p.Arg106Gln)	rs1200121142
NM_004281.4(BAG3):c.467C>G (p.Ala156Gly)	rs572038196
NM_004281.4(BAG3):c.49G>C (p.Gly17Arg)	rs727502895
NM_004281.4(BAG3):c.533A>G (p.Asp178Gly)
NM_004281.4(BAG3):c.55C>A (p.Arg19Ser)	rs727502896
NM_004281.4(BAG3):c.695A>T (p.His232Leu)	rs746241240
NM_004281.4(BAG3):c.784G>A (p.Ala262Thr)	rs876661343
NM_004281.4(BAG3):c.910-10C>G	rs727502899

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