ClinVar Miner

List of variants in gene ETFB reported as likely 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: 8
Download table as spreadsheet
NM_001985.3(ETFB):c.253C>A (p.Arg85=) rs187424345
NM_001985.3(ETFB):c.292C>T (p.Arg98Cys) rs147353781
NM_001985.3(ETFB):c.452C>T (p.Ser151Phe) rs74735908
NM_001985.3(ETFB):c.521G>A (p.Arg174His) rs141917423
NM_001985.3(ETFB):c.565G>A (p.Glu189Lys) rs376065198
NM_001985.3(ETFB):c.577G>A (p.Ala193Thr) rs200186078
NM_001985.3(ETFB):c.58-212A>C rs143144671
NM_001985.3(ETFB):c.58-318_58-313dup rs61361626

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.