List of variants studied for Mitochondrial DNA depletion syndrome 13 by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001278716.2(FBXL4):c.1232G>A (p.Cys411Tyr)	rs773850151	0.00014
NM_001278716.2(FBXL4):c.64C>T (p.Arg22Ter)	rs200440128	0.00005
NM_001278716.2(FBXL4):c.1288C>T (p.Arg430Ter)	rs758395213	0.00003
NM_001278716.2(FBXL4):c.616C>T (p.Arg206Ter)	rs964532159	0.00001
NM_001278716.2(FBXL4):c.929T>C (p.Leu310Pro)	rs2128393288

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.