ClinVar Miner

List of variants in gene PPOX studied for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP
NM_001122764.3(PPOX):c.-128C>G rs72714915
NM_001122764.3(PPOX):c.-149G>T rs186428034
NM_001122764.3(PPOX):c.-151G>T rs115158839
NM_001122764.3(PPOX):c.-174A>G rs886045451
NM_001122764.3(PPOX):c.-180T>C rs886045450
NM_001122764.3(PPOX):c.-1C>T rs148045152
NM_001122764.3(PPOX):c.-246G>T rs114493458
NM_001122764.3(PPOX):c.-247C>A rs2301286
NM_001122764.3(PPOX):c.-251G>C rs368129128
NM_001122764.3(PPOX):c.-2G>T rs779526273
NM_001122764.3(PPOX):c.1062T>C (p.Pro354=) rs771215757
NM_001122764.3(PPOX):c.1087C>G (p.Leu363Val) rs886045455
NM_001122764.3(PPOX):c.1248+4A>G rs775748399
NM_001122764.3(PPOX):c.1303C>T (p.Gln435Ter) rs754313121
NM_001122764.3(PPOX):c.175C>T (p.Arg59Trp) rs121918324
NM_001122764.3(PPOX):c.199del (p.Ala66_Leu67insTer) rs786204784
NM_001122764.3(PPOX):c.338+9A>G rs886045453
NM_001122764.3(PPOX):c.35T>C (p.Ile12Thr) rs28936677
NM_001122764.3(PPOX):c.360C>T (p.Pro120=) rs148730591
NM_001122764.3(PPOX):c.471+3G>A rs200920978
NM_001122764.3(PPOX):c.502C>T (p.Arg168Cys) rs121918325
NM_001122764.3(PPOX):c.503G>A (p.Arg168His) rs41270025
NM_001122764.3(PPOX):c.522C>T (p.Asn174=) rs886045454
NM_001122764.3(PPOX):c.538_539del (p.Ile180fs)
NM_001122764.3(PPOX):c.590T>C (p.Ile197Thr) rs1553238545
NM_001122764.3(PPOX):c.59A>C (p.His20Pro) rs121918326
NM_001122764.3(PPOX):c.617-6C>T rs200192089
NM_001122764.3(PPOX):c.646A>G (p.Ile216Val) rs758572020
NM_001122764.3(PPOX):c.694G>C (p.Gly232Arg) rs121918323
NM_001122764.3(PPOX):c.69G>T (p.Arg23=) rs886045452
NM_001122764.3(PPOX):c.869-3_869-2del rs1558033572
NM_001122764.3(PPOX):c.87+13C>T rs201155115
NM_001122764.3(PPOX):c.911G>A (p.Arg304His) rs36013429
NM_001122764.3(PPOX):c.936G>A (p.Val312=) rs751511778
PPOX, 1-BP INS, 1022G
PPOX, 5-BP DEL, NT1239

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.