ClinVar Miner

List of variants in gene SUOX reported as uncertain significance for amino acid or protein metabolism disease with epilepsy

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP
NC_000012.12:g.56005531G>C
NM_000456.2(SUOX):c.-322C>T rs886049678
NM_001032386.2(SUOX):c.*155C>T rs530553316
NM_001032386.2(SUOX):c.*187G>T rs886049684
NM_001032386.2(SUOX):c.*26C>G rs770314090
NM_001032386.2(SUOX):c.*311A>G
NM_001032386.2(SUOX):c.*355T>C rs886049685
NM_001032386.2(SUOX):c.*369G>A
NM_001032386.2(SUOX):c.*479T>C
NM_001032386.2(SUOX):c.*47A>C
NM_001032386.2(SUOX):c.*496T>C rs569168288
NM_001032386.2(SUOX):c.-11+1672T>A rs886049681
NM_001032386.2(SUOX):c.-11+1723G>A rs373341778
NM_001032386.2(SUOX):c.-129A>G
NM_001032386.2(SUOX):c.-25G>C rs886049680
NM_001032386.2(SUOX):c.-58C>A rs886049679
NM_001032386.2(SUOX):c.-85G>A rs773650494
NM_001032386.2(SUOX):c.1137A>G (p.Lys379=)
NM_001032386.2(SUOX):c.119G>A (p.Arg40His)
NM_001032386.2(SUOX):c.1247C>T (p.Ser416Phe) rs886049683
NM_001032386.2(SUOX):c.1282G>A (p.Ala428Thr) rs553699159
NM_001032386.2(SUOX):c.1306G>A (p.Glu436Lys) rs142424431
NM_001032386.2(SUOX):c.1333A>G (p.Ile445Val)
NM_001032386.2(SUOX):c.1388_1389CT[1] (p.Leu464fs)
NM_001032386.2(SUOX):c.1527G>A (p.Lys509=)
NM_001032386.2(SUOX):c.1586G>A (p.Arg529Gln) rs754321646
NM_001032386.2(SUOX):c.1612C>T (p.Arg538Cys)
NM_001032386.2(SUOX):c.186A>T (p.Leu62Phe) rs1347179760
NM_001032386.2(SUOX):c.192C>T (p.Leu64=) rs577360771
NM_001032386.2(SUOX):c.199G>C (p.Val67Leu)
NM_001032386.2(SUOX):c.228+1G>A
NM_001032386.2(SUOX):c.228G>T (p.Arg76Ser) rs202085145
NM_001032386.2(SUOX):c.23T>C (p.Val8Ala) rs537720526
NM_001032386.2(SUOX):c.279C>T (p.His93=) rs763253683
NM_001032386.2(SUOX):c.364C>G (p.Pro122Ala) rs886049682
NM_001032386.2(SUOX):c.50+9G>A rs368327991
NM_001032386.2(SUOX):c.507C>T (p.Thr169=) rs765012855
NM_001032386.2(SUOX):c.51-14G>A
NM_001032386.2(SUOX):c.574C>T (p.Arg192Trp)
NM_001032386.2(SUOX):c.621C>T (p.Tyr207=)
NM_001032386.2(SUOX):c.713C>T (p.Pro238Leu)
NM_001032386.2(SUOX):c.889C>T (p.Arg297Trp) rs767916239
NM_001032386.2(SUOX):c.890G>A (p.Arg297Gln)
NM_001032386.2(SUOX):c.89G>C (p.Cys30Ser)
NM_001032386.2(SUOX):c.931G>A (p.Glu311Lys) rs778950352
NM_001032386.2(SUOX):c.968C>T (p.Ser323Leu) rs143457531
NM_001032386.2(SUOX):c.983C>T (p.Thr328Ile) rs540792428

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.