ClinVar Miner

List of variants in gene ACADM reported as benign for acyl-CoA dehydrogenase deficiency

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_000016.5(ACADM):c.*39G>A rs17848065
NM_000016.5(ACADM):c.*672T>C rs8763
NM_000016.5(ACADM):c.*773G>A rs61612438
NM_000016.5(ACADM):c.*77C>T rs143911981
NM_000016.5(ACADM):c.*878T>C rs1146587
NM_000016.5(ACADM):c.-34T>C rs59932454
NM_000016.5(ACADM):c.1161A>G (p.Val387=) rs1061337
NM_000016.5(ACADM):c.118+114A>G rs875989868
NM_000016.5(ACADM):c.118+18T>A rs755405418
NM_000016.5(ACADM):c.118+60del rs796117827
NM_000016.5(ACADM):c.118+64del rs875989853
NM_000016.5(ACADM):c.119-20T>C rs74090724
NM_000016.5(ACADM):c.216+10T>C rs2275378
NM_000016.5(ACADM):c.31-37C>T rs201590881
NM_000016.5(ACADM):c.31-73T>C rs142795930
NM_000016.5(ACADM):c.351A>C (p.Thr117=) rs74090726
NM_000016.5(ACADM):c.468+62C>T rs875989870
NM_000016.5(ACADM):c.468+71T>C rs571856182
NM_000016.5(ACADM):c.469-9A>G rs181322317
NM_000016.5(ACADM):c.489T>G (p.Pro163=) rs78392995
NM_000016.5(ACADM):c.678A>G (p.Ala226=) rs2229249
NM_000016.5(ACADM):c.900C>T (p.Thr300=) rs17097429

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.