ClinVar Miner

List of variants in gene NOD2 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 160
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HGVS dbSNP
NM_001370466.1(NOD2):c.-8-2184G>A rs771671839
NM_001370466.1(NOD2):c.-8-2223del
NM_001370466.1(NOD2):c.-8-2238G>C rs976567823
NM_001370466.1(NOD2):c.-8-2243T>C rs765406921
NM_001370466.1(NOD2):c.1003del (p.Asp335fs)
NM_001370466.1(NOD2):c.1006A>T (p.Ile336Phe) rs104895470
NM_001370466.1(NOD2):c.1022T>C (p.Leu341Pro)
NM_001370466.1(NOD2):c.1036C>T (p.Arg346Cys) rs145293873
NM_001370466.1(NOD2):c.1058G>A (p.Gly353Asp)
NM_001370466.1(NOD2):c.1070T>A (p.Phe357Tyr) rs777343284
NM_001370466.1(NOD2):c.1087G>A (p.Asp363Asn)
NM_001370466.1(NOD2):c.1096C>T (p.Arg366Cys)
NM_001370466.1(NOD2):c.1097G>A (p.Arg366His) rs140918872
NM_001370466.1(NOD2):c.1109C>T (p.Pro370Leu) rs150078153
NM_001370466.1(NOD2):c.1118C>T (p.Pro373Leu)
NM_001370466.1(NOD2):c.1124C>T (p.Ser375Phe)
NM_001370466.1(NOD2):c.1160A>G (p.Asn387Ser) rs104895429
NM_001370466.1(NOD2):c.1190C>A (p.Thr397Asn) rs1596864349
NM_001370466.1(NOD2):c.1196G>A (p.Arg399His) rs562225614
NM_001370466.1(NOD2):c.1198C>T (p.Pro400Ser) rs760982375
NM_001370466.1(NOD2):c.119C>G (p.Ser40Cys) rs146149433
NM_001370466.1(NOD2):c.1214C>T (p.Ala405Val) rs2076754
NM_001370466.1(NOD2):c.1240G>A (p.Glu414Lys) rs104895432
NM_001370466.1(NOD2):c.1309G>T (p.Gly437Trp) rs104895492
NM_001370466.1(NOD2):c.1321C>A (p.Arg441Ser) rs769988393
NM_001370466.1(NOD2):c.1322G>A (p.Arg441His)
NM_001370466.1(NOD2):c.133G>A (p.Glu45Lys)
NM_001370466.1(NOD2):c.1340A>G (p.Gln447Arg)
NM_001370466.1(NOD2):c.1346C>A (p.Thr449Asn) rs1567392113
NM_001370466.1(NOD2):c.1379T>A (p.Val460Asp)
NM_001370466.1(NOD2):c.1413A>C (p.Glu471Asp) rs1361409611
NM_001370466.1(NOD2):c.1418T>A (p.Leu473Ter)
NM_001370466.1(NOD2):c.1434del (p.Ser479fs) rs754761524
NM_001370466.1(NOD2):c.1434dup (p.Ser479fs) rs754761524
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.1492G>A (p.Ala498Thr) rs1283801598
NM_001370466.1(NOD2):c.1529C>T (p.Pro510Leu)
NM_001370466.1(NOD2):c.1540C>T (p.Arg514Trp) rs576658764
NM_001370466.1(NOD2):c.1546C>T (p.Arg516Cys)
NM_001370466.1(NOD2):c.1547G>A (p.Arg516His) rs772534917
NM_001370466.1(NOD2):c.1567C>G (p.Leu523Val) rs104895471
NM_001370466.1(NOD2):c.1609G>A (p.Val537Met)
NM_001370466.1(NOD2):c.1616C>T (p.Ser539Leu)
NM_001370466.1(NOD2):c.1639C>G (p.Gln547Glu)
NM_001370466.1(NOD2):c.1679G>A (p.Arg560His) rs373185098
NM_001370466.1(NOD2):c.1706C>T (p.Thr569Met) rs142077546
NM_001370466.1(NOD2):c.1745T>G (p.Phe582Cys) rs777798807
NM_001370466.1(NOD2):c.1753G>T (p.Ala585Ser) rs104895438
NM_001370466.1(NOD2):c.178C>T (p.Arg60Cys) rs374128251
NM_001370466.1(NOD2):c.1828_1846del (p.Asn610fs)
NM_001370466.1(NOD2):c.1852C>A (p.Pro618Thr)
NM_001370466.1(NOD2):c.1888A>G (p.Ser630Gly) rs150236752
NM_001370466.1(NOD2):c.1894G>A (p.Val632Met)
NM_001370466.1(NOD2):c.1923del (p.His642fs)
NM_001370466.1(NOD2):c.193G>T (p.Val65Phe) rs187264529
NM_001370466.1(NOD2):c.1957G>A (p.Gly653Arg) rs371339573
NM_001370466.1(NOD2):c.1994A>G (p.Glu665Gly)
NM_001370466.1(NOD2):c.1A>G (p.Met1Val) rs372321755
NM_001370466.1(NOD2):c.2026C>G (p.Arg676Gly)
NM_001370466.1(NOD2):c.2029C>T (p.Gln677Ter)
NM_001370466.1(NOD2):c.2066G>A (p.Arg689His) rs200035357
NM_001370466.1(NOD2):c.2087C>T (p.Pro696Leu) rs201076024
NM_001370466.1(NOD2):c.2099C>T (p.Pro700Leu) rs104895489
NM_001370466.1(NOD2):c.2149C>T (p.Arg717Trp) rs140876663
NM_001370466.1(NOD2):c.2161G>A (p.Glu721Lys) rs757403209
NM_001370466.1(NOD2):c.2171A>G (p.Glu724Gly)
NM_001370466.1(NOD2):c.2176C>T (p.Arg726Trp) rs749720540
NM_001370466.1(NOD2):c.2185C>T (p.Arg729Trp) rs376201089
NM_001370466.1(NOD2):c.2186G>A (p.Arg729Gln) rs375713299
NM_001370466.1(NOD2):c.2197C>T (p.Arg733Cys) rs3813758
NM_001370466.1(NOD2):c.2198G>A (p.Arg733His) rs763955590
NM_001370466.1(NOD2):c.2226G>C (p.Leu742Phe)
NM_001370466.1(NOD2):c.2251G>A (p.Glu751Lys) rs104895443
NM_001370466.1(NOD2):c.2294C>G (p.Pro765Arg)
NM_001370466.1(NOD2):c.22C>T (p.Gln8Ter) rs1567380372
NM_001370466.1(NOD2):c.230T>C (p.Ile77Thr)
NM_001370466.1(NOD2):c.2323G>A (p.Val775Met)
NM_001370466.1(NOD2):c.2338G>A (p.Val780Met) rs748522514
NM_001370466.1(NOD2):c.233C>T (p.Ala78Val) rs202052365
NM_001370466.1(NOD2):c.2353C>T (p.Pro785Ser) rs746692864
NM_001370466.1(NOD2):c.2363G>T (p.Gly788Val)
NM_001370466.1(NOD2):c.2390A>G (p.Asp797Gly) rs778481419
NM_001370466.1(NOD2):c.2393A>G (p.Asn798Ser)
NM_001370466.1(NOD2):c.2407C>T (p.Arg803Ter)
NM_001370466.1(NOD2):c.2413A>G (p.Ile805Val) rs765335094
NM_001370466.1(NOD2):c.2419A>C (p.Lys807Gln)
NM_001370466.1(NOD2):c.2434G>T (p.Ala812Ser)
NM_001370466.1(NOD2):c.2443T>C (p.Cys815Arg)
NM_001370466.1(NOD2):c.2465+1G>A rs373550987
NM_001370466.1(NOD2):c.2465+2dup rs748508924
NM_001370466.1(NOD2):c.2465C>T (p.Ala822Val) rs104895486
NM_001370466.1(NOD2):c.2466-8C>G
NM_001370466.1(NOD2):c.2497G>A (p.Ala833Thr) rs754270929
NM_001370466.1(NOD2):c.2528G>A (p.Arg843Lys)
NM_001370466.1(NOD2):c.2558A>G (p.Asn853Ser)
NM_001370466.1(NOD2):c.256G>A (p.Asp86Asn) rs104895468
NM_001370466.1(NOD2):c.2577G>A (p.Ala859=) rs1417676866
NM_001370466.1(NOD2):c.2596G>A (p.Glu866Lys)
NM_001370466.1(NOD2):c.2605C>T (p.Arg869Ter)
NM_001370466.1(NOD2):c.2618C>T (p.Ser873Phe) rs199552944
NM_001370466.1(NOD2):c.2654G>C (p.Gly885Ala)
NM_001370466.1(NOD2):c.2690G>A (p.Gly897Asp) rs104895453
NM_001370466.1(NOD2):c.2693A>G (p.Asp898Gly) rs545734771
NM_001370466.1(NOD2):c.2734A>G (p.Ile912Val) rs201781416
NM_001370466.1(NOD2):c.2752C>T (p.Gln918Ter)
NM_001370466.1(NOD2):c.2776A>G (p.Lys926Glu)
NM_001370466.1(NOD2):c.2792A>G (p.Glu931Gly)
NM_001370466.1(NOD2):c.2802-9T>A rs750873269
NM_001370466.1(NOD2):c.2807A>G (p.Glu936Gly) rs1555501675
NM_001370466.1(NOD2):c.2840C>T (p.Ser947Phe) rs200463498
NM_001370466.1(NOD2):c.2842C>G (p.Leu948Val) rs1337759230
NM_001370466.1(NOD2):c.2845G>A (p.Ala949Thr) rs148561632
NM_001370466.1(NOD2):c.2852G>A (p.Gly951Glu) rs104895457
NM_001370466.1(NOD2):c.2903T>C (p.Ile968Thr)
NM_001370466.1(NOD2):c.2915G>C (p.Gly972Ala) rs1238071864
NM_001370466.1(NOD2):c.2917G>A (p.Ala973Thr) rs1282634444
NM_001370466.1(NOD2):c.2929C>G (p.Leu977Val)
NM_001370466.1(NOD2):c.2938C>T (p.Leu980Phe)
NM_001370466.1(NOD2):c.2944A>G (p.Arg982Gly)
NM_001370466.1(NOD2):c.295C>G (p.His99Asp)
NM_001370466.1(NOD2):c.2971C>T (p.Leu991Phe)
NM_001370466.1(NOD2):c.2974C>G (p.Arg992Gly)
NM_001370466.1(NOD2):c.2975G>A (p.Arg992Gln)
NM_001370466.1(NOD2):c.2975G>T (p.Arg992Leu)
NM_001370466.1(NOD2):c.3001G>A (p.Val1001Ile)
NM_001370466.1(NOD2):c.323_324AG[1] (p.His110fs) rs1567381106
NM_001370466.1(NOD2):c.332G>A (p.Arg111Gln) rs104895456
NM_001370466.1(NOD2):c.394C>T (p.Arg132Trp)
NM_001370466.1(NOD2):c.395G>A (p.Arg132Gln) rs150996156
NM_001370466.1(NOD2):c.417A>T (p.Glu139Asp)
NM_001370466.1(NOD2):c.437C>T (p.Pro146Leu)
NM_001370466.1(NOD2):c.43G>C (p.Val15Leu)
NM_001370466.1(NOD2):c.449C>T (p.Pro150Leu)
NM_001370466.1(NOD2):c.461C>A (p.Ala154Glu)
NM_001370466.1(NOD2):c.46G>A (p.Glu16Lys) rs200089552
NM_001370466.1(NOD2):c.494C>T (p.Ala165Val)
NM_001370466.1(NOD2):c.497A>G (p.Asn166Ser)
NM_001370466.1(NOD2):c.50T>A (p.Leu17Gln) rs757914381
NM_001370466.1(NOD2):c.544C>T (p.Pro182Ser) rs143080077
NM_001370466.1(NOD2):c.59C>T (p.Ser20Leu) rs201586544
NM_001370466.1(NOD2):c.616C>T (p.Gln206Ter)
NM_001370466.1(NOD2):c.617A>C (p.Gln206Pro) rs369098290
NM_001370466.1(NOD2):c.622C>T (p.Arg208Cys) rs104895422
NM_001370466.1(NOD2):c.631A>G (p.Ser211Gly)
NM_001370466.1(NOD2):c.631A>T (p.Ser211Cys) rs1001861018
NM_001370466.1(NOD2):c.638A>G (p.Tyr213Cys) rs202190367
NM_001370466.1(NOD2):c.659G>T (p.Cys220Phe)
NM_001370466.1(NOD2):c.665A>G (p.Glu222Gly) rs117836686
NM_001370466.1(NOD2):c.706G>A (p.Val236Met)
NM_001370466.1(NOD2):c.781del (p.Leu261fs)
NM_001370466.1(NOD2):c.821C>T (p.Ala274Val) rs104895426
NM_001370466.1(NOD2):c.839C>T (p.Thr280Met)
NM_001370466.1(NOD2):c.841C>T (p.Leu281Phe)
NM_001370466.1(NOD2):c.845T>C (p.Leu282Pro)
NM_001370466.1(NOD2):c.8C>G (p.Ser3Trp)
NM_001370466.1(NOD2):c.938C>G (p.Ala313Gly) rs774016655
NM_001370466.1(NOD2):c.947T>C (p.Leu316Pro) rs369732140
NM_001370466.1(NOD2):c.956G>A (p.Arg319Gln)
NM_001370466.1(NOD2):c.989A>G (p.Asp330Gly)

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