List of variants in gene ACADM reported as benign for Medium-chain acyl-coenzyme A dehydrogenase deficiency

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: 36

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.*878T>C	rs1146587	0.65645
NM_000016.6(ACADM):c.286+178G>A	rs3818855	0.30613
NM_000016.6(ACADM):c.387+32C>G	rs2153126	0.30601
NM_000016.6(ACADM):c.216+10T>C	rs2275378	0.30596
NM_000016.6(ACADM):c.469-22C>A	rs12127402	0.25202
NM_000016.6(ACADM):c.31-32C>G	rs7524467	0.23867
NM_000016.6(ACADM):c.945+99T>C	rs11161521	0.23825
NM_000016.6(ACADM):c.1161A>G (p.Val387=)	rs1061337	0.23824
NM_000016.6(ACADM):c.*672T>C	rs8763	0.14503
NM_000016.6(ACADM):c.-362T>C	rs1251076	0.12826
NM_000016.6(ACADM):c.-34T>C	rs59932454	0.05213
NM_000016.6(ACADM):c.119-20T>C	rs74090724	0.05208
NM_000016.6(ACADM):c.351A>C (p.Thr117=)	rs74090726	0.05204
NM_000016.6(ACADM):c.*773G>A	rs61612438	0.05111
NM_000016.6(ACADM):c.-401G>A	rs114005461	0.04873
NM_000016.6(ACADM):c.-142C>G	rs61124994	0.04520
NM_000016.6(ACADM):c.*39G>A	rs17848065	0.04004
NM_000016.6(ACADM):c.31-73T>C	rs142795930	0.02211
NM_000016.6(ACADM):c.489T>G (p.Pro163=)	rs78392995	0.02136
NM_000016.6(ACADM):c.900C>T (p.Thr300=)	rs17097429	0.01131
NM_000016.6(ACADM):c.*77C>T	rs143911981	0.00652
NM_000016.6(ACADM):c.387+40G>A	rs187510227	0.00241
NM_000016.6(ACADM):c.31-37C>T	rs201590881	0.00224
NM_000016.6(ACADM):c.469-9A>G	rs181322317	0.00223
NM_000016.6(ACADM):c.468+71T>C	rs571856182	0.00198
NM_000016.6(ACADM):c.678A>G (p.Ala226=)	rs2229249	0.00108
NM_000016.6(ACADM):c.1194+11A>G	rs373059851	0.00084
NM_000016.6(ACADM):c.468+62C>T	rs875989870	0.00019
NM_000016.6(ACADM):c.118+18T>A	rs755405418	0.00003
NM_000016.5(ACADM):c.-257G>A	rs17848068
NM_000016.6(ACADM):c.118+114A>G	rs875989868
NM_000016.6(ACADM):c.118+60del	rs796117827
NM_000016.6(ACADM):c.118+64del	rs875989853
NM_000016.6(ACADM):c.1194+23del
NM_000016.6(ACADM):c.1194+23dup
NM_000016.6(ACADM):c.1195-8dup

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.