ClinVar Miner

List of variants in gene NOD2 studied for not provided

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Gene type:
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Total variants: 39
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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.1001G>A (p.Arg334Gln) rs104895461
NM_022162.3(NOD2):c.1031C>T (p.Ser344Phe) rs199475912
NM_022162.3(NOD2):c.1258C>T (p.Arg420Cys) rs367883043
NM_022162.3(NOD2):c.1259G>A (p.Arg420His) rs199475913
NM_022162.3(NOD2):c.1281G>A (p.Pro427=) rs104895430
NM_022162.3(NOD2):c.1321G>A (p.Glu441Lys) rs104895432
NM_022162.3(NOD2):c.1540T>C (p.Tyr514His) rs540122692
NM_022162.3(NOD2):c.2004G>A (p.Pro668=) rs199475914
NM_022162.3(NOD2):c.2107C>T (p.Arg703Cys) rs5743277
NM_022162.3(NOD2):c.2137C>T (p.Arg713Cys) rs104895440
NM_022162.3(NOD2):c.2138G>A (p.Arg713His) rs104895483
NM_022162.3(NOD2):c.2262G>A (p.Leu754=) rs199475915
NM_022162.3(NOD2):c.2264C>T (p.Ala755Val) rs61747625
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.2555A>G (p.Asn852Ser) rs104895467
NM_022162.3(NOD2):c.2576dup (p.Cys859fs) rs1555500626
NM_022162.3(NOD2):c.2631-316A>G rs199475921
NM_022162.3(NOD2):c.2798+148A>G rs199475922
NM_022162.3(NOD2):c.2851C>G (p.Leu951Val)
NM_022162.3(NOD2):c.566C>T (p.Thr189Met) rs61755182
NM_022162.3(NOD2):c.60C>T (p.Leu20=) rs144993105
NM_022162.3(NOD2):c.631G>T (p.Ala211Ser) rs771887760
NM_022162.3(NOD2):c.646+1G>A rs766614906
NM_022162.3(NOD2):c.73+151T>C rs199475911
NM_022162.3(NOD2):c.807G>A (p.Pro269=) rs369766454
NM_022162.3(NOD2):c.931C>T (p.Arg311Trp) rs104895427

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