ClinVar Miner

List of variants in gene NLRP3 reported as benign for not provided

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Gene type:
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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_001243133.2(NLRP3):c.780A>G (p.Arg260=) rs4925543 0.92770
NM_001243133.2(NLRP3):c.2493-40G>A rs10754557 0.50722
NM_001243133.2(NLRP3):c.3005+44C>A rs45624634 0.12875
NM_001243133.2(NLRP3):c.2150+59G>A rs3738447 0.12565
NM_001243133.2(NLRP3):c.2321+85A>G rs12060377 0.11467
NM_001243133.2(NLRP3):c.657C>T (p.Thr219=) rs7525979 0.10943
NM_001243133.2(NLRP3):c.1302C>T (p.Ser434=) rs34298354 0.08679
NM_001243133.2(NLRP3):c.780= (p.Arg260=) rs4925543 0.07230
NM_001243133.2(NLRP3):c.-40G>T rs73136263 0.03689
NM_001243133.2(NLRP3):c.2107C>A (p.Gln703Lys) rs35829419 0.03262
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met) rs121908147 0.00835
NM_001243133.2(NLRP3):c.423C>T (p.Tyr141=) rs56710146 0.00680
NM_001243133.2(NLRP3):c.3005+25C>T rs61841189 0.00667
NM_001243133.2(NLRP3):c.278-45T>C rs41303141 0.00639
NM_001243133.2(NLRP3):c.1231C>T (p.Leu411=) rs148478875 0.00638
NM_001243133.2(NLRP3):c.1600C>T (p.Leu534=) rs116054301 0.00596
NM_001243133.2(NLRP3):c.1020C>T (p.Pro340=) rs41311573 0.00548
NM_001243133.2(NLRP3):c.1389C>T (p.His463=) rs111400208 0.00354
NM_001243133.2(NLRP3):c.397+7G>A rs192297357 0.00350
NM_001243133.2(NLRP3):c.277+89T>A rs866873824 0.00170
NM_001243133.2(NLRP3):c.1119G>A (p.Glu373=) rs138613962 0.00139
NM_001243133.2(NLRP3):c.789C>T (p.Ser263=) rs146442638 0.00089
NM_001243133.2(NLRP3):c.930C>T (p.Asp310=) rs143840033 0.00076
NM_001243133.2(NLRP3):c.1463G>A (p.Arg488Lys) rs145268073 0.00070
NM_001243133.2(NLRP3):c.1639A>T (p.Ser547Cys) rs139833874 0.00061
NM_001243133.2(NLRP3):c.2855C>T (p.Thr952Met) rs139814109 0.00051
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly) rs147946775 0.00049
NM_001243133.2(NLRP3):c.1245C>T (p.Ile415=) rs139852370 0.00045
NM_001243133.2(NLRP3):c.1032G>A (p.Leu344=) rs180177471 0.00039
NM_001243133.2(NLRP3):c.1383C>T (p.Cys461=) rs104895398 0.00020
NM_001243133.2(NLRP3):c.564C>T (p.Ile188=) rs147631017 0.00020
NM_001243133.2(NLRP3):c.2364C>A (p.Ile788=) rs766840708 0.00013
NM_001243133.2(NLRP3):c.1200C>T (p.Asn400=) rs202094185 0.00010
NM_001243133.2(NLRP3):c.2150+77C>G rs1298480596 0.00009
NM_001243133.2(NLRP3):c.2493-44C>T rs190033492 0.00009
NM_001243133.2(NLRP3):c.3005+7G>A rs200659209 0.00009
NM_001243133.2(NLRP3):c.1044G>A (p.Thr348=) rs143140947 0.00007
NM_001243133.2(NLRP3):c.1665C>T (p.Asp555=) rs151097783 0.00007
NM_001243133.2(NLRP3):c.2150+16T>C rs368389907 0.00006
NM_001243133.2(NLRP3):c.2709C>G (p.Ser903=) rs145787821 0.00006
NM_001243133.2(NLRP3):c.398-15C>T rs200906786 0.00006
NM_001243133.2(NLRP3):c.1362G>C (p.Gly454=) rs200314422 0.00002
NM_001243133.2(NLRP3):c.2419G>A (p.Ala807Thr) rs201096167 0.00002
NM_001243133.2(NLRP3):c.*1G>T rs2103261881
NM_001243133.2(NLRP3):c.-79C>T rs2103083187
NM_001243133.2(NLRP3):c.1554C>T (p.Phe518=) rs2103111350
NM_001243133.2(NLRP3):c.2150+98A>G rs2103114731
NM_001243133.2(NLRP3):c.2151-5C>G rs2103132130
NM_001243133.2(NLRP3):c.2322-155T>C rs113427259
NM_001243133.2(NLRP3):c.2492+54C>T rs72771997
NM_001243133.2(NLRP3):c.2505C>T (p.Cys835=) rs1351993448
NM_001243133.2(NLRP3):c.2834+37T>C rs1664438506
NM_001243133.2(NLRP3):c.2835-10del rs1558210190
NM_001243133.2(NLRP3):c.2862C>T (p.His954=) rs2103237927
NM_001243133.2(NLRP3):c.398-49C>T rs1362265668
NM_001243133.2(NLRP3):c.726G>A (p.Ala242=) rs3806268
NM_001243133.2(NLRP3):c.810G>A (p.Leu270=) rs2103107257

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