ClinVar Miner

List of variants in gene NLRP3 reported as likely benign

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_001079821.2(NLRP3):c.381C>A
NM_004895.4(NLRP3):c.-116T>C rs202234129
NM_004895.4(NLRP3):c.-225G>A rs138900557
NM_004895.4(NLRP3):c.-454G>A rs199475727
NM_004895.4(NLRP3):c.-527C>T rs141994679
NM_004895.4(NLRP3):c.-537A>T rs116502550
NM_004895.4(NLRP3):c.-704C>T rs199723383
NM_004895.4(NLRP3):c.1026C>T (p.Pro342=) rs41311573
NM_004895.4(NLRP3):c.1038G>A (p.Leu346=) rs180177471
NM_004895.4(NLRP3):c.1050G>A (p.Thr350=) rs143140947
NM_004895.4(NLRP3):c.1122C>T (p.Ser374=) rs374056197
NM_004895.4(NLRP3):c.1125G>A (p.Glu375=) rs138613962
NM_004895.4(NLRP3):c.1237C>T (p.Leu413=) rs148478875
NM_004895.4(NLRP3):c.1251C>T (p.Ile417=) rs139852370
NM_004895.4(NLRP3):c.1311G>A (p.Lys437=) rs1553286808
NM_004895.4(NLRP3):c.1323G>A (p.Ala441=) rs201976178
NM_004895.4(NLRP3):c.1329C>T (p.Tyr443=) rs200269703
NM_004895.4(NLRP3):c.1380C>T (p.His460=) rs180177481
NM_004895.4(NLRP3):c.1395C>T (p.His465=) rs111400208
NM_004895.4(NLRP3):c.1407C>T (p.Leu469=) rs141637807
NM_004895.4(NLRP3):c.1469G>A (p.Arg490Lys) rs145268073
NM_004895.4(NLRP3):c.1494T>C (p.Asp498=) rs1372355086
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.1806G>A (p.Gln602=) rs1018524884
NM_004895.4(NLRP3):c.1848C>G (p.Ala616=)
NM_004895.4(NLRP3):c.1926C>T (p.Phe642=) rs34698071
NM_004895.4(NLRP3):c.201G>A (p.Ala67=) rs201205620
NM_004895.4(NLRP3):c.209T>C (p.Met70Thr) rs147559626
NM_004895.4(NLRP3):c.2138A>T (p.His713Leu) rs767805817
NM_004895.4(NLRP3):c.213C>T (p.Ala71=) rs200082602
NM_004895.4(NLRP3):c.214G>A (p.Val72Met) rs117287351
NM_004895.4(NLRP3):c.2154T>C (p.His718=) rs199592175
NM_004895.4(NLRP3):c.2156+12C>T
NM_004895.4(NLRP3):c.2157-11C>T rs201019209
NM_004895.4(NLRP3):c.2157-16T>A rs1057524463
NM_004895.4(NLRP3):c.2178T>A (p.Thr726=) rs201102829
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.2191C>A (p.Arg731=) rs148590318
NM_004895.4(NLRP3):c.2220C>T (p.Ser740=) rs183128734
NM_004895.4(NLRP3):c.225C>T (p.Phe75=) rs201980166
NM_004895.4(NLRP3):c.2307C>G (p.Gly769=) rs150229101
NM_004895.4(NLRP3):c.2327+11G>A rs371752834
NM_004895.4(NLRP3):c.2328-6A>G rs778792605
NM_004895.4(NLRP3):c.2430C>T (p.Leu810=) rs147154764
NM_004895.4(NLRP3):c.2463A>T (p.Gly821=) rs202034848
NM_004895.4(NLRP3):c.2494C>A (p.Leu832Ile) rs114158404
NM_004895.4(NLRP3):c.2498+13C>T rs199746830
NM_004895.4(NLRP3):c.2498+8G>A rs201453934
NM_004895.4(NLRP3):c.255G>A (p.Glu85=) rs375070491
NM_004895.4(NLRP3):c.2709T>G (p.Ala903=) rs138089800
NM_004895.4(NLRP3):c.2817C>T (p.Pro939=) rs545121784
NM_004895.4(NLRP3):c.283+11G>A rs577522959
NM_004895.4(NLRP3):c.2861C>T (p.Thr954Met) rs139814109
NM_004895.4(NLRP3):c.3011+25C>T rs61841189
NM_004895.4(NLRP3):c.375G>A (p.Ser125=) rs750104265
NM_004895.4(NLRP3):c.403+7G>A rs192297357
NM_004895.4(NLRP3):c.404-5C>T rs200459664
NM_004895.4(NLRP3):c.429C>T (p.Tyr143=) rs56710146
NM_004895.4(NLRP3):c.531C>T (p.His177=) rs376196301
NM_004895.4(NLRP3):c.576G>A (p.Lys192=) rs1553286256
NM_004895.4(NLRP3):c.585G>A (p.Thr195=) rs149659331
NM_004895.4(NLRP3):c.593G>A (p.Ser198Asn) rs180177459
NM_004895.4(NLRP3):c.598G>A (p.Val200Met) rs121908147
NM_004895.4(NLRP3):c.624G>A (p.Leu208=) rs201463849
NM_004895.4(NLRP3):c.624G>T (p.Leu208=) rs201463849
NM_004895.4(NLRP3):c.680C>T (p.Ala227Val) rs180177493
NM_004895.4(NLRP3):c.795C>T (p.Ser265=) rs146442638
NM_004895.4(NLRP3):c.906C>T (p.Asp302=) rs145826369
NM_004895.4(NLRP3):c.912C>T (p.Phe304=) rs756989752
NM_004895.4(NLRP3):c.936C>T (p.Asp312=) rs143840033
NM_004895.4(NLRP3):c.950C>T (p.Pro317Leu) rs180177462

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