ClinVar Miner

List of variants in gene BAG3 reported as uncertain significance for Myofibrillar Myopathy, Dominant

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_004281.3(BAG3):c.*399G>T rs774188346
NM_004281.3(BAG3):c.-285C>A rs866276705
NM_004281.3(BAG3):c.-285C>T rs866276705
NM_004281.3(BAG3):c.-87G>T rs879223257
NM_004281.3(BAG3):c.1214C>T (p.Ala405Val) rs11199064
NM_004281.3(BAG3):c.1298A>G (p.Gln433Arg) rs886046755
NM_004281.3(BAG3):c.1503C>T (p.Val501=) rs147277075
NM_004281.3(BAG3):c.1571T>C (p.Ile524Thr) rs752390475
NM_004281.3(BAG3):c.1588G>A (p.Val530Met) rs144678100
NM_004281.3(BAG3):c.1634C>G (p.Pro545Arg) rs759348679
NM_004281.3(BAG3):c.1667C>A (p.Ala556Glu) rs886046756
NM_004281.3(BAG3):c.465A>G (p.Ala155=) rs775151738
NM_004281.3(BAG3):c.554C>T (p.Ser185Leu) rs730880054
NM_004281.3(BAG3):c.564G>T (p.Leu188=) rs886046754
NM_004281.3(BAG3):c.855G>A (p.Thr285=) rs147259596

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.