ClinVar Miner

List of variants in gene NLRP3 reported as benign

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Gene type:
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Total variants: 39
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HGVS dbSNP
NM_001079821.2(NLRP3):c.1085T>A
NM_004895.4(NLRP3):c.*177del rs796764638
NM_004895.4(NLRP3):c.*230G>C rs10754558
NM_004895.4(NLRP3):c.*351dup rs397821684
NM_004895.4(NLRP3):c.*396T>A rs10802501
NM_004895.4(NLRP3):c.*489C>T rs10802502
NM_004895.4(NLRP3):c.-34G>T rs73136263
NM_004895.4(NLRP3):c.-405T>C rs7523422
NM_004895.4(NLRP3):c.-555T>G rs72771992
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.1308C>T (p.Ser436=) rs34298354
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.1590C>T (p.Ala530=) rs201644343
NM_004895.4(NLRP3):c.1606C>T (p.Leu536=) rs116054301
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.2124C>T (p.Leu708=) rs149493236
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.2157-7T>C rs116546330
NM_004895.4(NLRP3):c.2349G>A (p.Ser783=) rs764753476
NM_004895.4(NLRP3):c.284-45T>C rs41303141
NM_004895.4(NLRP3):c.3011+25C>T rs61841189
NM_004895.4(NLRP3):c.306G>A (p.Ser102=) rs149161277
NM_004895.4(NLRP3):c.315T>C (p.Thr105=) rs199822721
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.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.786G>A (p.Arg262=) rs4925543
NM_004895.4(NLRP3):c.795C>T (p.Ser265=) rs146442638
NM_004895.4(NLRP3):c.936C>T (p.Asp312=) rs143840033

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