ClinVar Miner

List of variants in gene NOD2 studied for not provided

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Gene type:
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Total variants: 79
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HGVS dbSNP
NM_001370466.1(NOD2):c.*8G>A rs199475923
NM_001370466.1(NOD2):c.-8-2185C>T rs144993105
NM_001370466.1(NOD2):c.-8-2232G>C rs140977130
NM_001370466.1(NOD2):c.-8-2619C>A rs199475907
NM_001370466.1(NOD2):c.-9+2758A>G rs199475906
NM_001370466.1(NOD2):c.1041C>T (p.Val347=) rs757517796
NM_001370466.1(NOD2):c.1091G>A (p.Arg364His) rs554887705
NM_001370466.1(NOD2):c.1110G>A (p.Pro370=) rs766883774
NM_001370466.1(NOD2):c.1188G>A (p.Val396=) rs77966199
NM_001370466.1(NOD2):c.1200G>A (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1200G>C (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu) rs104895431
NM_001370466.1(NOD2):c.1235G>A (p.Arg412His) rs143110172
NM_001370466.1(NOD2):c.1239C>T (p.Thr413=) rs143395754
NM_001370466.1(NOD2):c.1240G>A (p.Glu414Lys) rs104895432
NM_001370466.1(NOD2):c.1242G>A (p.Glu414=) rs1224862712
NM_001370466.1(NOD2):c.1245C>T (p.Phe415=) rs151315883
NM_001370466.1(NOD2):c.1293G>A (p.Lys431=) rs1430003119
NM_001370466.1(NOD2):c.1450A>G (p.Thr484Ala) rs759153904
NM_001370466.1(NOD2):c.1459T>C (p.Tyr487His) rs540122692
NM_001370466.1(NOD2):c.1497C>G (p.Thr499=) rs779950802
NM_001370466.1(NOD2):c.1563G>A (p.Leu521=) rs369085294
NM_001370466.1(NOD2):c.1678C>T (p.Arg560Cys) rs104895479
NM_001370466.1(NOD2):c.1755G>A (p.Ala585=) rs756626309
NM_001370466.1(NOD2):c.1848C>T (p.Leu616=) rs764199623
NM_001370466.1(NOD2):c.1906C>T (p.Leu636=) rs762922997
NM_001370466.1(NOD2):c.1923G>A (p.Pro641=) rs199475914
NM_001370466.1(NOD2):c.2026C>T (p.Arg676Cys) rs5743277
NM_001370466.1(NOD2):c.2056C>T (p.Arg686Cys) rs104895440
NM_001370466.1(NOD2):c.2057G>A (p.Arg686His) rs104895483
NM_001370466.1(NOD2):c.2130C>T (p.Pro710=) rs769210593
NM_001370466.1(NOD2):c.216C>T (p.Ala72=) rs1398956455
NM_001370466.1(NOD2):c.2176C>T (p.Arg726Trp) rs749720540
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val) rs61747625
NM_001370466.1(NOD2):c.2223G>A (p.Lys741=) rs1596871165
NM_001370466.1(NOD2):c.2296G>A (p.Val766Met) rs104895444
NM_001370466.1(NOD2):c.2474A>G (p.Asn825Ser) rs104895467
NM_001370466.1(NOD2):c.2490C>T (p.Asp830=) rs144083291
NM_001370466.1(NOD2):c.255C>A (p.Ala85=) rs770046355
NM_001370466.1(NOD2):c.2586A>C (p.Gln862His) rs764244331
NM_001370466.1(NOD2):c.2641G>C (p.Gly881Arg) rs2066845
NM_001370466.1(NOD2):c.2641G>T (p.Gly881Cys) rs2066845
NM_001370466.1(NOD2):c.2717+158C>T rs5743289
NM_001370466.1(NOD2):c.2721G>A (p.Leu907=) rs149691662
NM_001370466.1(NOD2):c.2881C>T (p.Leu961=) rs1596908135
NM_001370466.1(NOD2):c.2931G>A (p.Leu977=) rs773388366
NM_001370466.1(NOD2):c.347G>A (p.Arg116Lys) rs1596827607
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met) rs61755182
NM_001370466.1(NOD2):c.486G>A (p.Thr162=) rs144887729
NM_001370466.1(NOD2):c.510C>T (p.Ala170=) rs765729513
NM_001370466.1(NOD2):c.539C>G (p.Pro180Arg) rs1596852030
NM_001370466.1(NOD2):c.550G>T (p.Ala184Ser) rs771887760
NM_001370466.1(NOD2):c.726G>A (p.Pro242=) rs369766454
NM_001370466.1(NOD2):c.789C>T (p.Asp263=) rs749180535
NM_001370466.1(NOD2):c.815G>A (p.Gly272Asp)
NM_001370466.1(NOD2):c.850C>T (p.Arg284Trp) rs104895427
NM_001370466.1(NOD2):c.920G>A (p.Arg307Gln) rs104895461
NM_001370466.1(NOD2):c.9G>A (p.Ser3=) rs774491311
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.-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.1258C>T (p.Arg420Cys) rs367883043
NM_022162.3(NOD2):c.1259G>A (p.Arg420His) rs199475913
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.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) rs768561004
NM_022162.3(NOD2):c.646+1G>A rs766614906
NM_022162.3(NOD2):c.73+151T>C rs199475911

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