ClinVar Miner

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

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Gene type:
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Total variants: 48
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HGVS dbSNP
NM_022162.2(NOD2):c.1028T>C (p.Leu343Pro)
NM_022162.2(NOD2):c.103C>T (p.Gln35Ter)
NM_022162.2(NOD2):c.1087A>T (p.Ile363Phe) rs104895470
NM_022162.2(NOD2):c.1151T>A (p.Phe384Tyr)
NM_022162.2(NOD2):c.1178G>A (p.Arg393His)
NM_022162.2(NOD2):c.1190C>T (p.Pro397Leu) rs150078153
NM_022162.2(NOD2):c.1241A>G (p.Asn414Ser) rs104895429
NM_022162.2(NOD2):c.1277G>A (p.Arg426His) rs562225614
NM_022162.2(NOD2):c.1279C>T (p.Pro427Ser) rs760982375
NM_022162.2(NOD2):c.127G>A (p.Glu43Lys) rs200089552
NM_022162.2(NOD2):c.1316G>A (p.Arg439His) rs143110172
NM_022162.2(NOD2):c.1321G>A (p.Glu441Lys) rs104895432
NM_022162.2(NOD2):c.1402C>A (p.Arg468Ser)
NM_022162.2(NOD2):c.140C>T (p.Ser47Leu) rs201586544
NM_022162.2(NOD2):c.1427C>A (p.Thr476Asn)
NM_022162.2(NOD2):c.1494A>C (p.Glu498Asp)
NM_022162.2(NOD2):c.1515delG (p.Ser506Profs)
NM_022162.2(NOD2):c.1515dup (p.Ser506Valfs) rs754761524
NM_022162.2(NOD2):c.1573G>A (p.Ala525Thr)
NM_022162.2(NOD2):c.1628G>A (p.Arg543His)
NM_022162.2(NOD2):c.1760G>A (p.Arg587His)
NM_022162.2(NOD2):c.1969A>G (p.Ser657Gly)
NM_022162.2(NOD2):c.2038G>A (p.Gly680Arg) rs371339573
NM_022162.2(NOD2):c.2050C>T (p.Arg684Trp) rs5743276
NM_022162.2(NOD2):c.2266C>T (p.Arg756Trp)
NM_022162.2(NOD2):c.2267G>A (p.Arg756Gln)
NM_022162.2(NOD2):c.2279G>A (p.Arg760His)
NM_022162.2(NOD2):c.2332G>A (p.Glu778Lys) rs104895443
NM_022162.2(NOD2):c.2419G>A (p.Val807Met)
NM_022162.2(NOD2):c.2494A>G (p.Ile832Val) rs765335094
NM_022162.2(NOD2):c.259C>T (p.Arg87Cys)
NM_022162.2(NOD2):c.2658G>A (p.Ala886=) rs1417676866
NM_022162.2(NOD2):c.2699C>T (p.Ser900Phe) rs199552944
NM_022162.2(NOD2):c.2774A>G (p.Asp925Gly)
NM_022162.2(NOD2):c.2883-9T>A
NM_022162.2(NOD2):c.2888A>G (p.Glu963Gly) rs1555501675
NM_022162.2(NOD2):c.2921C>T (p.Ser974Phe) rs200463498
NM_022162.2(NOD2):c.2926G>A (p.Ala976Thr) rs148561632
NM_022162.2(NOD2):c.2T>C (p.Met1Thr) rs765406921
NM_022162.2(NOD2):c.314C>T (p.Ala105Val) rs202052365
NM_022162.2(NOD2):c.406_407delAG (p.His137Profs)
NM_022162.2(NOD2):c.413G>A (p.Arg138Gln) rs104895456
NM_022162.2(NOD2):c.476G>A (p.Arg159Gln) rs150996156
NM_022162.2(NOD2):c.625C>T (p.Pro209Ser)
NM_022162.2(NOD2):c.698A>C (p.Gln233Pro) rs369098290
NM_022162.2(NOD2):c.712A>T (p.Ser238Cys) rs1001861018
NM_022162.2(NOD2):c.746A>G (p.Glu249Gly) rs117836686
NM_022162.2(NOD2):c.7G>C (p.Glu3Gln) rs976567823

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