ClinVar Miner

List of variants in gene NOD2 reported as uncertain significance for not provided

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Total variants: 21
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HGVS dbSNP
NM_001370466.1(NOD2):c.1200G>A (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1235G>A (p.Arg412His) rs143110172
NM_001370466.1(NOD2):c.1240G>A (p.Glu414Lys) rs104895432
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.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.2176C>T (p.Arg726Trp) rs749720540
NM_001370466.1(NOD2):c.2474A>G (p.Asn825Ser) rs104895467
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.347G>A (p.Arg116Lys) rs1596827607
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met) rs61755182
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.815G>A (p.Gly272Asp)
NM_001370466.1(NOD2):c.850C>T (p.Arg284Trp) rs104895427
NM_022162.3(NOD2):c.1258C>T (p.Arg420Cys) rs367883043
NM_022162.3(NOD2):c.2576dup (p.Cys859fs) rs1555500626
NM_022162.3(NOD2):c.2851C>G (p.Leu951Val) rs768561004

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