List of variants in gene BAG3 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.1296A>G (p.Val432=)	rs196295	0.75935
NM_004281.4(BAG3):c.*218G>C	rs8946	0.38461
NM_004281.4(BAG3):c.*535A>G	rs11199065	0.19554
NM_004281.4(BAG3):c.451T>C (p.Cys151Arg)	rs2234962	0.14532
NM_004281.4(BAG3):c.1220C>T (p.Pro407Leu)	rs3858340	0.12393
NM_004281.4(BAG3):c.1002T>G (p.Pro334=)	rs3858339	0.12375
NM_004281.4(BAG3):c.-284G>C	rs192502283	0.01069
NM_004281.4(BAG3):c.-271C>T	rs144814361	0.00867
NM_004281.4(BAG3):c.*31C>T	rs116329258	0.00853
NM_004281.4(BAG3):c.231G>A (p.Pro77=)	rs143752613	0.00441
NM_004281.4(BAG3):c.606G>T (p.Pro202=)	rs74157690	0.00341
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr)	rs61756328	0.00239
NM_004281.4(BAG3):c.-17G>A	rs200388926	0.00218
NM_004281.4(BAG3):c.1587C>T (p.Ala529=)	rs149358702	0.00144
NM_004281.4(BAG3):c.549C>G (p.Ser183=)	rs112929734	0.00141
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val)	rs34656239	0.00097
NM_004281.4(BAG3):c.855G>A (p.Thr285=)	rs147259596	0.00048
NM_004281.4(BAG3):c.888C>T (p.His296=)	rs139399890	0.00040
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp)	rs117671123	0.00036
NM_004281.4(BAG3):c.381A>T (p.Ala127=)	rs140594879	0.00030
NM_004281.4(BAG3):c.1240G>A (p.Glu414Lys)	rs117749531	0.00024
NM_004281.4(BAG3):c.1588G>A (p.Val530Met)	rs144678100	0.00016
NM_004281.4(BAG3):c.1634C>G (p.Pro545Arg)	rs759348679	0.00014
NM_004281.4(BAG3):c.1029C>A (p.Arg343=)	rs117972572	0.00013
NM_004281.4(BAG3):c.415C>T (p.Arg139Trp)	rs556465096	0.00011
NM_004281.4(BAG3):c.400T>A (p.Ser134Thr)	rs375257731	0.00006
NM_004281.4(BAG3):c.181-15C>T	rs397516882	0.00004
NM_004281.4(BAG3):c.*240GTT[1]	rs3981124
NM_004281.4(BAG3):c.306_307del	rs796515184
NM_004281.4(BAG3):c.*319C>T	rs148967962
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)	rs35434411
NM_004281.4(BAG3):c.467C>G (p.Ala156Gly)	rs572038196

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