ClinVar Miner

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

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Gene type:
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Total variants: 42
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HGVS dbSNP
NM_001243133.2(NLRP3):c.270G>A (p.Pro90=) rs771343047
NM_001243133.2(NLRP3):c.3005+25C>T rs61841189
NM_001243133.2(NLRP3):c.729G>A (p.Ser243=)
NM_004895.4(NLRP3):c.1005C>A (p.Leu335=) rs762774277
NM_004895.4(NLRP3):c.1311G>A (p.Lys437=) rs1553286808
NM_004895.4(NLRP3):c.1320C>T (p.Thr440=) rs201210274
NM_004895.4(NLRP3):c.1329C>T (p.Tyr443=) rs200269703
NM_004895.4(NLRP3):c.1359C>T (p.Pro453=) rs200228309
NM_004895.4(NLRP3):c.1371C>T (p.Ser457=) rs777985232
NM_004895.4(NLRP3):c.1407C>T (p.Leu469=) rs141637807
NM_004895.4(NLRP3):c.1446C>A (p.Ile482=) rs756162800
NM_004895.4(NLRP3):c.1494T>C (p.Asp498=) rs1372355086
NM_004895.4(NLRP3):c.1651T>C (p.Leu551=) rs144469697
NM_004895.4(NLRP3):c.1680C>T (p.Val560=) rs1572172738
NM_004895.4(NLRP3):c.1848C>G (p.Ala616=) rs1410028681
NM_004895.4(NLRP3):c.1893C>T (p.Phe631=) rs1572173453
NM_004895.4(NLRP3):c.1900T>C (p.Leu634=) rs762299624
NM_004895.4(NLRP3):c.1905C>T (p.Tyr635=) rs200089426
NM_004895.4(NLRP3):c.209T>C (p.Met70Thr) rs147559626
NM_004895.4(NLRP3):c.2156+12C>T rs201291967
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.2328-6A>T rs778792605
NM_004895.4(NLRP3):c.2475G>A (p.Leu825=) rs1572200907
NM_004895.4(NLRP3):c.2498+7C>T rs200534219
NM_004895.4(NLRP3):c.2498+8G>A rs201453934
NM_004895.4(NLRP3):c.2499-8T>A rs199858933
NM_004895.4(NLRP3):c.2505C>T (p.Val835=) rs1572205424
NM_004895.4(NLRP3):c.2511C>T (p.Cys837=) rs1351993448
NM_004895.4(NLRP3):c.2577A>G (p.Arg859=) rs1248156475
NM_004895.4(NLRP3):c.2616C>T (p.Val872=) rs140618467
NM_004895.4(NLRP3):c.2715C>T (p.Ser905=) rs145787821
NM_004895.4(NLRP3):c.2784G>C (p.Gly928=) rs1201650200
NM_004895.4(NLRP3):c.2817C>T (p.Pro939=) rs545121784
NM_004895.4(NLRP3):c.284-10T>C rs184042335
NM_004895.4(NLRP3):c.284-6T>C rs756926136
NM_004895.4(NLRP3):c.3090C>T (p.Val1030=) rs201532680
NM_004895.4(NLRP3):c.403+7G>A rs192297357
NM_004895.4(NLRP3):c.531C>T (p.His177=) rs376196301
NM_004895.4(NLRP3):c.598G>A (p.Val200Met) rs121908147
NM_004895.4(NLRP3):c.612G>A (p.Lys204=) rs146606931
NM_004895.4(NLRP3):c.633C>T (p.Pro211=) rs554444159
NM_004895.4(NLRP3):c.732G>T (p.Ala244=) rs3806268

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