ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
NM_004281.3(BAG3):c.-359C>T rs186893240
NM_004281.3(BAG3):c.-518C>T rs11199059
NM_004281.3(BAG3):c.-543T>C rs140579074
NM_004281.3(BAG3):c.180+264G>A rs112168846
NM_004281.3(BAG3):c.180+269C>G rs2577336
NM_004281.3(BAG3):c.181-107A>G rs2240777
NM_004281.3(BAG3):c.181-291A>G rs7900065
NM_004281.3(BAG3):c.468_470GGC[4] (p.Ala160dup) rs139438727
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp) rs117671123
NM_004281.3(BAG3):c.898G>A (p.Asp300Asn) rs78439745
NM_004281.3(BAG3):c.909+272C>A rs2072361
NM_004281.4(BAG3):c.1002T>G (p.Pro334=) rs3858339
NM_004281.4(BAG3):c.1138C>T (p.Pro380Ser) rs144692954
NM_004281.4(BAG3):c.1220C>T (p.Pro407Leu) rs3858340
NM_004281.4(BAG3):c.1296A>G (p.Val432=) rs196295
NM_004281.4(BAG3):c.187C>G (p.Pro63Ala) rs144041999
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln) rs35434411
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr) rs61756328
NM_004281.4(BAG3):c.606G>T (p.Pro202=) rs74157690

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.