ClinVar Miner

List of variants reported as benign for Sulfite oxidase deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001032386.2(SUOX):c.-32C>T rs705703 0.01929
NM_001032386.2(SUOX):c.-107C>T rs114410290 0.00602
NM_001032386.2(SUOX):c.1358G>A (p.Gly453Asp) rs76537761 0.00392
NM_001032386.2(SUOX):c.629C>T (p.Pro210Leu) rs141735896 0.00351
NM_001032386.2(SUOX):c.228G>T (p.Arg76Ser) rs202085145 0.00057
NM_001032386.2(SUOX):c.119G>A (p.Arg40His) rs117778870 0.00049
NM_001032386.2(SUOX):c.1050T>C (p.Tyr350=) rs184819190 0.00027
NM_001032386.2(SUOX):c.51-14G>A rs141432255 0.00017
NM_001032386.2(SUOX):c.977C>A (p.Thr326Asn) rs540920017 0.00002
NM_001032386.2(SUOX):c.1281G>C (p.Ser427=) rs773115
NM_001032386.2(SUOX):c.1281G>T (p.Ser427=) rs773115
NM_001032386.2(SUOX):c.1636T>A (p.Ter546Arg) rs574353697
NM_001032386.2(SUOX):c.621C>T (p.Tyr207=) rs144469629

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.