ClinVar Miner

List of variants in gene NLRP3 reported as likely benign for not specified

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met) rs121908147 0.00835
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.789C>T (p.Ser263=) rs146442638 0.00089
NM_001243133.2(NLRP3):c.930C>T (p.Asp310=) rs143840033 0.00076
NM_001243133.2(NLRP3):c.1639A>T (p.Ser547Cys) rs139833874 0.00061
NM_001243133.2(NLRP3):c.2457A>T (p.Gly819=) rs202034848 0.00059
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.1645T>C (p.Leu549=) rs144469697 0.00038
NM_001243133.2(NLRP3):c.208G>A (p.Val70Met) rs117287351 0.00031
NM_001243133.2(NLRP3):c.404G>A (p.Arg135His) rs138946894 0.00029
NM_001243133.2(NLRP3):c.249G>A (p.Glu83=) rs375070491 0.00013
NM_001243133.2(NLRP3):c.906C>T (p.Phe302=) rs756989752 0.00011
NM_001243133.2(NLRP3):c.944C>T (p.Pro315Leu) rs180177462 0.00010
NM_001243133.2(NLRP3):c.1317G>A (p.Ala439=) rs201976178 0.00007
NM_001243133.2(NLRP3):c.1665C>T (p.Asp555=) rs151097783 0.00007
NM_001243133.2(NLRP3):c.277+11G>A rs577522959 0.00007
NM_001243133.2(NLRP3):c.1323C>T (p.Tyr441=) rs200269703 0.00006
NM_001243133.2(NLRP3):c.1361G>A (p.Gly454Glu) rs199696688 0.00006
NM_001243133.2(NLRP3):c.1116C>T (p.Ser372=) rs374056197 0.00004
NM_001243133.2(NLRP3):c.111C>T (p.Ile37=) rs145314485 0.00004
NM_001243133.2(NLRP3):c.2835-7T>G rs747303698 0.00004
NM_001243133.2(NLRP3):c.2321+11G>A rs371752834 0.00003
NM_001243133.2(NLRP3):c.2322-6A>G rs778792605 0.00002
NM_001243133.2(NLRP3):c.1800G>A (p.Gln600=) rs1018524884 0.00001
NM_001243133.2(NLRP3):c.2151-11C>T rs201019209 0.00001
NM_001243133.2(NLRP3):c.2321+12T>A rs747043119 0.00001
NM_001243133.2(NLRP3):c.2492+13C>T rs199746830 0.00001
NM_001243133.2(NLRP3):c.2492+8G>A rs201453934 0.00001
NM_001243133.2(NLRP3):c.2811C>T (p.Pro937=) rs545121784 0.00001
NM_001243133.2(NLRP3):c.369G>A (p.Ser123=) rs750104265 0.00001
NM_001243133.2(NLRP3):c.195G>A (p.Ala65=) rs201205620
NM_001243133.2(NLRP3):c.2132A>T (p.His711Leu) rs767805817
NM_001243133.2(NLRP3):c.2151-16T>A rs1057524463
NM_001243133.2(NLRP3):c.2172T>A (p.Thr724=) rs201102829
NM_001243133.2(NLRP3):c.2343G>T (p.Ser781=) rs764753476
NM_001243133.2(NLRP3):c.375C>A (p.Ile125=) rs758069883
NM_001243133.2(NLRP3):c.51T>C (p.Asp17=) rs1572151908
NM_001243133.2(NLRP3):c.570G>A (p.Lys190=) rs1553286256
NM_001243133.2(NLRP3):c.618G>A (p.Leu206=) rs201463849

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