List of variants in gene ACADM reported by Genome-Nilou Lab

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
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.1161A>G (p.Val387=)	rs1061337	0.23824
NM_000016.6(ACADM):c.945+99T>C	rs11161521	0.23506
NM_000016.6(ACADM):c.*39G>A	rs17848065	0.03869
NM_000016.6(ACADM):c.31-73T>C	rs142795930	0.02212
NM_000016.6(ACADM):c.994C>T (p.Leu332=)	rs138098371	0.00093
NM_000016.6(ACADM):c.-257G>A	rs17848068
NM_000016.6(ACADM):c.1103T>C (p.Leu368Ser)	rs2100453501
NM_000016.6(ACADM):c.118+60del	rs796117827
NM_000016.6(ACADM):c.139G>A (p.Glu47Lys)	rs2100362559

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.