ClinVar Miner

List of variants in gene NLRP3 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 34
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HGVS dbSNP
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.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.1380C>T (p.His460=) rs180177481
NM_004895.4(NLRP3):c.1395C>T (p.His465=) rs111400208
NM_004895.4(NLRP3):c.1469G>A (p.Arg490Lys) rs145268073
NM_004895.4(NLRP3):c.1606C>T (p.Leu536=) rs116054301
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
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.950C>T (p.Pro317Leu) rs180177462

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