ClinVar Miner

List of variants in gene NLRP3 reported as likely benign for Chronic infantile neurological, cutaneous and articular syndrome

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Total variants: 31
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HGVS dbSNP
NM_001079821.2(NLRP3):c.-39+51G>A rs199475727
NM_001243133.1(NLRP3):c.1032G>A (p.Leu344=) rs180177471
NM_001243133.1(NLRP3):c.1231C>T (p.Leu411=) rs148478875
NM_001243133.1(NLRP3):c.1374C>T (p.His458=) rs180177481
NM_001243133.1(NLRP3):c.1389C>T (p.His463=) rs111400208
NM_001243133.1(NLRP3):c.1600C>T (p.Leu534=) rs116054301
NM_001243133.1(NLRP3):c.587G>A (p.Ser196Asn) rs180177459
NM_001243133.1(NLRP3):c.944C>T (p.Pro315Leu) rs180177462
NM_004895.4(NLRP3):c.-116T>C rs202234129
NM_004895.4(NLRP3):c.-225G>A rs138900557
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.1050G>A (p.Thr350=) rs143140947
NM_004895.4(NLRP3):c.1125G>A (p.Glu375=) rs138613962
NM_004895.4(NLRP3):c.1251C>T (p.Ile417=) rs139852370
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.209T>C (p.Met70Thr) rs147559626
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.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.2307C>G (p.Gly769=) rs150229101
NM_004895.4(NLRP3):c.2430C>T (p.Leu810=) rs147154764
NM_004895.4(NLRP3):c.283+11G>A rs577522959
NM_004895.4(NLRP3):c.2861C>T (p.Thr954Met) rs139814109
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

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