ClinVar Miner

List of variants in gene NLRP3 reported by Invitae

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Gene type:
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Total variants: 50
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HGVS dbSNP
NM_001243133.1(NLRP3):c.1020C>T (p.Pro340=) rs41311573
NM_001243133.1(NLRP3):c.1032G>A (p.Leu344=) rs180177471
NM_001243133.1(NLRP3):c.1043C>T (p.Thr348Met) rs151344629
NM_001243133.1(NLRP3):c.1231C>T (p.Leu411=) rs148478875
NM_001243133.1(NLRP3):c.1306A>G (p.Thr436Ala) rs180177465
NM_001243133.1(NLRP3):c.1316C>T (p.Ala439Val) rs121908146
NM_001243133.1(NLRP3):c.1389C>T (p.His463=) rs111400208
NM_001243133.1(NLRP3):c.1463G>A (p.Arg488Lys) rs145268073
NM_001243133.1(NLRP3):c.1600C>T (p.Leu534=) rs116054301
NM_001243133.1(NLRP3):c.592G>A (p.Val198Met) rs121908147
NM_001243133.1(NLRP3):c.674C>T (p.Ala225Val) rs180177493
NM_001243133.1(NLRP3):c.907G>A (p.Asp303Asn) rs121908153
NM_001243133.1(NLRP3):c.930C>T (p.Asp310=) rs143840033
NM_001243133.1(NLRP3):c.937A>G (p.Ile313Val) rs180177501
NM_004895.4(NLRP3):c.1096C>T (p.Arg366Trp) rs994458759
NM_004895.4(NLRP3):c.1125G>A (p.Glu375=) rs138613962
NM_004895.4(NLRP3):c.1181C>A (p.Ala394Glu) rs1553286687
NM_004895.4(NLRP3):c.1192C>G (p.Leu398Val) rs906785956
NM_004895.4(NLRP3):c.1407C>T (p.Leu469=) rs141637807
NM_004895.4(NLRP3):c.1645A>T (p.Ser549Cys) rs139833874
NM_004895.4(NLRP3):c.1667G>A (p.Arg556Gln)
NM_004895.4(NLRP3):c.1820A>T (p.Glu607Val)
NM_004895.4(NLRP3):c.2101C>T (p.Leu701Phe)
NM_004895.4(NLRP3):c.2113C>A (p.Gln705Lys) rs35829419
NM_004895.4(NLRP3):c.2126C>A (p.Pro709Gln)
NM_004895.4(NLRP3):c.2140G>T (p.Ala714Ser)
NM_004895.4(NLRP3):c.214G>A (p.Val72Met) rs117287351
NM_004895.4(NLRP3):c.2154T>C (p.His718=) rs199592175
NM_004895.4(NLRP3):c.2157-7T>C rs116546330
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.225C>T (p.Phe75=) rs201980166
NM_004895.4(NLRP3):c.230C>T (p.Ala77Val) rs200288250
NM_004895.4(NLRP3):c.2349G>A (p.Ser783=) rs764753476
NM_004895.4(NLRP3):c.2494C>A (p.Leu832Ile) rs114158404
NM_004895.4(NLRP3):c.2582A>C (p.Tyr861Ser) rs180177452
NM_004895.4(NLRP3):c.2617G>A (p.Ala873Thr) rs201867582
NM_004895.4(NLRP3):c.2709T>G (p.Ala903=) rs138089800
NM_004895.4(NLRP3):c.2759G>A (p.Arg920Gln) rs1553293095
NM_004895.4(NLRP3):c.2825A>G (p.Lys942Arg) rs201580005
NM_004895.4(NLRP3):c.299G>A (p.Arg100His) rs201887896
NM_004895.4(NLRP3):c.3043A>G (p.Lys1015Glu) rs771315000
NM_004895.4(NLRP3):c.403+7G>A rs192297357
NM_004895.4(NLRP3):c.429C>T (p.Tyr143=) rs56710146
NM_004895.4(NLRP3):c.437G>A (p.Ser146Asn)
NM_004895.4(NLRP3):c.585G>A (p.Thr195=) rs149659331
NM_004895.4(NLRP3):c.616G>A (p.Glu206Lys)
NM_004895.4(NLRP3):c.624G>T (p.Leu208=) rs201463849
NM_004895.4(NLRP3):c.721T>A (p.Leu241Met)
NM_004895.4(NLRP3):c.786G>A (p.Arg262=) rs4925543
NM_004895.4(NLRP3):c.906C>T (p.Asp302=) rs145826369

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