List of variants reported as uncertain significance for combined oxidative phosphorylation defect type 8 by Baylor Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020745.4(AARS2):c.1162C>T (p.Pro388Ser)	rs139372744	0.00220
NM_020745.4(AARS2):c.533C>T (p.Ala178Val)	rs200343365	0.00043
NM_020745.4(AARS2):c.1157C>T (p.Ala386Val)	rs143271585	0.00019
NM_020745.4(AARS2):c.679G>A (p.Asp227Asn)	rs765016818	0.00009
NM_020745.4(AARS2):c.2266C>T (p.Arg756Cys)	rs753324375	0.00007
NM_020745.4(AARS2):c.2561G>A (p.Arg854His)	rs751611980	0.00003
NM_020745.4(AARS2):c.31_39del (p.Leu12_Arg14del)	rs562829310
NM_020745.4(AARS2):c.472C>A (p.Gln158Lys)	rs759138272
NM_020745.4(AARS2):c.649C>T (p.Pro217Ser)	rs1786310363

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.