ClinVar Miner

List of variants in gene NOD1 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP
NM_001354849.1(NOD1):c.-585G>C rs199475895
NM_006092.3(NOD1):c.-523-142G>A rs199475894
NM_006092.3(NOD1):c.-523-629C>T rs199475893
NM_006092.4(NOD1):c.-121-85G>C rs199476262
NM_006092.4(NOD1):c.-211+198G>A rs199476261
NM_006092.4(NOD1):c.-234G>A rs199475896
NM_006092.4(NOD1):c.1369C>T (p.Arg457Trp) rs199475900
NM_006092.4(NOD1):c.1423C>T (p.Leu475Phe) rs199475901
NM_006092.4(NOD1):c.1458C>T (p.Ser486=) rs199475902
NM_006092.4(NOD1):c.1492del (p.Leu498fs) rs199476263
NM_006092.4(NOD1):c.2080G>A (p.Ala694Thr) rs199475903
NM_006092.4(NOD1):c.2201+36C>T rs199476264
NM_006092.4(NOD1):c.2202-27C>T rs199476265
NM_006092.4(NOD1):c.2285+112G>A rs199476268
NM_006092.4(NOD1):c.2285+118C>T rs199476269
NM_006092.4(NOD1):c.2285+220T>A rs199476270
NM_006092.4(NOD1):c.2285+31T>C rs199476266
NM_006092.4(NOD1):c.2285+372T>A rs199475904
NM_006092.4(NOD1):c.2285+90G>A rs199476267
NM_006092.4(NOD1):c.2454-116G>C rs199476271
NM_006092.4(NOD1):c.2537+169A>C rs199476273
NM_006092.4(NOD1):c.2537+344C>G rs199476274
NM_006092.4(NOD1):c.2537+394T>A rs199476275
NM_006092.4(NOD1):c.2537+81G>A rs199476272
NM_006092.4(NOD1):c.254T>A (p.Phe85Tyr) rs199475897
NM_006092.4(NOD1):c.2697G>C (p.Lys899Asn) rs199475905
NM_006092.4(NOD1):c.285T>C (p.Asp95=) rs199475898
NM_006092.4(NOD1):c.375A>G (p.Pro125=) rs199475899

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.