ClinVar Miner

List of variants in gene NLRP3 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001243133.2(NLRP3):c.1020C>T (p.Pro340=) rs41311573 0.00548
NM_001243133.2(NLRP3):c.2488C>A (p.Leu830Ile) rs114158404 0.00083
NM_001243133.2(NLRP3):c.2457A>T (p.Gly819=) rs202034848 0.00059
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.525C>T (p.His175=) rs376196301 0.00021
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.1317G>A (p.Ala439=) rs201976178 0.00007
NM_001243133.2(NLRP3):c.225G>A (p.Ala75=) rs140219362 0.00007
NM_001243133.2(NLRP3):c.277+11G>A rs577522959 0.00007
NM_001243133.2(NLRP3):c.2940C>T (p.Gly980=) rs199649583 0.00007
NM_001243133.2(NLRP3):c.1323C>T (p.Tyr441=) rs200269703 0.00006
NM_001243133.2(NLRP3):c.2214C>T (p.Ser738=) rs183128734 0.00006
NM_001243133.2(NLRP3):c.2424C>T (p.Leu808=) rs147154764 0.00005
NM_001243133.2(NLRP3):c.1116C>T (p.Ser372=) rs374056197 0.00004
NM_001243133.2(NLRP3):c.2761A>G (p.Thr921Ala) rs200089542 0.00004
NM_001243133.2(NLRP3):c.171C>T (p.Ile57=) rs773673175 0.00003
NM_001243133.2(NLRP3):c.2150+12C>T rs201291967 0.00003
NM_001243133.2(NLRP3):c.2321+11G>A rs371752834 0.00003
NM_001243133.2(NLRP3):c.299C>T (p.Ser100Leu) rs776897356 0.00003
NM_001243133.2(NLRP3):c.2322-6A>G rs778792605 0.00002
NM_001243133.2(NLRP3):c.2856G>A (p.Thr952=) rs200474558 0.00002
NM_001243133.2(NLRP3):c.1800G>A (p.Gln600=) rs1018524884 0.00001
NM_001243133.2(NLRP3):c.2098G>A (p.Asp700Asn) rs781561828 0.00001
NM_001243133.2(NLRP3):c.2151-11C>T rs201019209 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.369G>A (p.Ser123=) rs750104265 0.00001
NM_001243133.2(NLRP3):c.1131A>G (p.Lys377=) rs755556220
NM_001243133.2(NLRP3):c.1374C>T (p.His458=) rs180177481
NM_001243133.2(NLRP3):c.1842C>G (p.Ala614=) rs1410028681
NM_001243133.2(NLRP3):c.195G>A (p.Ala65=) rs201205620
NM_001243133.2(NLRP3):c.2112T>C (p.Cys704=) rs2103114029
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.224C>T (p.Ala75Val) rs200288250
NM_001243133.2(NLRP3):c.570G>A (p.Lys190=) rs1553286256
NM_001243133.2(NLRP3):c.618G>A (p.Leu206=) rs201463849
NM_001243133.2(NLRP3):c.627C>T (p.Pro209=) rs554444159

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