ClinVar Miner

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

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Gene type:
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Total variants: 27
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HGVS dbSNP
NM_004895.4(NLRP3):c.1122C>T (p.Ser374=) rs374056197
NM_004895.4(NLRP3):c.1323G>A (p.Ala441=) rs201976178
NM_004895.4(NLRP3):c.1329C>T (p.Tyr443=) rs200269703
NM_004895.4(NLRP3):c.1380C>T (p.His460=) rs180177481
NM_004895.4(NLRP3):c.1651T>C (p.Leu551=) rs144469697
NM_004895.4(NLRP3):c.1806G>A (p.Gln602=) rs1018524884
NM_004895.4(NLRP3):c.1848C>G (p.Ala616=)
NM_004895.4(NLRP3):c.201G>A (p.Ala67=) rs201205620
NM_004895.4(NLRP3):c.2138A>T (p.His713Leu) rs767805817
NM_004895.4(NLRP3):c.214G>A (p.Val72Met) rs117287351
NM_004895.4(NLRP3):c.2156+12C>T
NM_004895.4(NLRP3):c.2157-11C>T rs201019209
NM_004895.4(NLRP3):c.2157-16T>A rs1057524463
NM_004895.4(NLRP3):c.2178T>A (p.Thr726=) rs201102829
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.2327+11G>A rs371752834
NM_004895.4(NLRP3):c.2328-6A>G rs778792605
NM_004895.4(NLRP3):c.2463A>T (p.Gly821=) rs202034848
NM_004895.4(NLRP3):c.2498+13C>T rs199746830
NM_004895.4(NLRP3):c.2498+8G>A rs201453934
NM_004895.4(NLRP3):c.255G>A (p.Glu85=) rs375070491
NM_004895.4(NLRP3):c.283+11G>A rs577522959
NM_004895.4(NLRP3):c.375G>A (p.Ser125=) rs750104265
NM_004895.4(NLRP3):c.531C>T (p.His177=) rs376196301
NM_004895.4(NLRP3):c.576G>A (p.Lys192=) rs1553286256
NM_004895.4(NLRP3):c.624G>A (p.Leu208=) rs201463849
NM_004895.4(NLRP3):c.912C>T (p.Phe304=) rs756989752

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