ClinVar Miner

List of variants in gene NOD2 reported by Human Evolutionary Genetics, Institut Pasteur

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP
NM_001370466.1(NOD2):c.-8-2619C>A rs199475907
NM_001370466.1(NOD2):c.-9+2758A>G rs199475906
NM_022162.3(NOD2):c.*192T>C rs199475925
NM_022162.3(NOD2):c.*214T>C rs199475926
NM_022162.3(NOD2):c.*80T>C rs199475924
NM_022162.3(NOD2):c.*8G>A rs199475923
NM_022162.3(NOD2):c.-144C>T rs199475909
NM_022162.3(NOD2):c.-162T>C rs199475908
NM_022162.3(NOD2):c.-91G>C rs199475910
NM_022162.3(NOD2):c.1031C>T (p.Ser344Phe) rs199475912
NM_022162.3(NOD2):c.1259G>A (p.Arg420His) rs199475913
NM_022162.3(NOD2):c.2004G>A (p.Pro668=) rs199475914
NM_022162.3(NOD2):c.2262G>A (p.Leu754=) rs199475915
NM_022162.3(NOD2):c.2418C>G (p.Gly806=) rs199475916
NM_022162.3(NOD2):c.2462+199A>G rs199475917
NM_022162.3(NOD2):c.2462+218A>G rs199475918
NM_022162.3(NOD2):c.2546+28G>A rs199475919
NM_022162.3(NOD2):c.2547-41G>A rs199475920
NM_022162.3(NOD2):c.2631-316A>G rs199475921
NM_022162.3(NOD2):c.2798+148A>G rs199475922
NM_022162.3(NOD2):c.73+151T>C rs199475911

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.