ClinVar Miner

List of variants in gene NLRP3 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 27
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HGVS dbSNP
NM_001079821.2(NLRP3):c.1085T>A
NM_001079821.2(NLRP3):c.381C>A
NM_004895.4(NLRP3):c.1026C>T (p.Pro342=) rs41311573
NM_004895.4(NLRP3):c.1050G>A (p.Thr350=) rs143140947
NM_004895.4(NLRP3):c.1237C>T (p.Leu413=) rs148478875
NM_004895.4(NLRP3):c.1308C>T (p.Ser436=) rs34298354
NM_004895.4(NLRP3):c.1395C>T (p.His465=) rs111400208
NM_004895.4(NLRP3):c.1606C>T (p.Leu536=) rs116054301
NM_004895.4(NLRP3):c.1645A>T (p.Ser549Cys) rs139833874
NM_004895.4(NLRP3):c.1651T>C (p.Leu551=) rs144469697
NM_004895.4(NLRP3):c.1926C>T (p.Phe642=) rs34698071
NM_004895.4(NLRP3):c.2113C>A (p.Gln705Lys) rs35829419
NM_004895.4(NLRP3):c.213C>T (p.Ala71=) rs200082602
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.2817C>T (p.Pro939=) rs545121784
NM_004895.4(NLRP3):c.3011+25C>T rs61841189
NM_004895.4(NLRP3):c.306G>A (p.Ser102=) rs149161277
NM_004895.4(NLRP3):c.403+7G>A rs192297357
NM_004895.4(NLRP3):c.429C>T (p.Tyr143=) rs56710146
NM_004895.4(NLRP3):c.598G>A (p.Val200Met) rs121908147
NM_004895.4(NLRP3):c.625T>C (p.Phe209Leu) rs776833139
NM_004895.4(NLRP3):c.663C>T (p.Thr221=) rs7525979
NM_004895.4(NLRP3):c.732G>A (p.Ala244=) rs3806268
NM_004895.4(NLRP3):c.786= (p.Arg262=) rs4925543
NM_004895.4(NLRP3):c.795C>T (p.Ser265=) rs146442638
NM_004895.4(NLRP3):c.912C>T (p.Phe304=) rs756989752
NM_004895.4(NLRP3):c.943A>G (p.Ile315Val) rs180177501

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