ClinVar Miner

List of variants in gene NLRP3 reported as uncertain significance for not provided

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Total variants: 50
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HGVS dbSNP
NM_004895.4(NLRP3):c.1027G>A (p.Glu343Lys) rs369910640
NM_004895.4(NLRP3):c.1070A>G (p.Lys357Arg) rs876660972
NM_004895.4(NLRP3):c.1303A>G (p.Thr435Ala) rs876661016
NM_004895.4(NLRP3):c.1339C>T (p.Leu447Phe) rs202121800
NM_004895.4(NLRP3):c.133C>T (p.Gln45Ter) rs1558185400
NM_004895.4(NLRP3):c.1469G>A (p.Arg490Lys) rs145268073
NM_004895.4(NLRP3):c.152A>G (p.His51Arg) rs367663649
NM_004895.4(NLRP3):c.1631C>T (p.Thr544Met) rs199856287
NM_004895.4(NLRP3):c.178G>A (p.Asp60Asn) rs1131691891
NM_004895.4(NLRP3):c.1845A>T (p.Lys615Asn) rs876660973
NM_004895.4(NLRP3):c.1942G>T (p.Asp648Tyr) rs138061418
NM_004895.4(NLRP3):c.200C>G (p.Ala67Gly) rs763252989
NM_004895.4(NLRP3):c.2113C>A (p.Gln705Lys) rs35829419
NM_004895.4(NLRP3):c.214G>A (p.Val72Met) rs117287351
NM_004895.4(NLRP3):c.2305G>A (p.Gly769Ser) rs866534904
NM_004895.4(NLRP3):c.230C>A (p.Ala77Glu) rs200288250
NM_004895.4(NLRP3):c.2383A>G (p.Ser795Gly) rs1064797023
NM_004895.4(NLRP3):c.2398C>A (p.Leu800Met) rs756392002
NM_004895.4(NLRP3):c.2431G>A (p.Gly811Ser) rs141389711
NM_004895.4(NLRP3):c.2494C>A (p.Leu832Ile) rs114158404
NM_004895.4(NLRP3):c.2542G>C (p.Ala848Pro) rs773376112
NM_004895.4(NLRP3):c.2617G>A (p.Ala873Thr) rs201867582
NM_004895.4(NLRP3):c.2674G>T (p.Val892Leu) rs193085132
NM_004895.4(NLRP3):c.2744C>T (p.Thr915Met) rs765925466
NM_004895.4(NLRP3):c.275C>T (p.Pro92Leu) rs145774400
NM_004895.4(NLRP3):c.2767A>G (p.Thr923Ala) rs200089542
NM_004895.4(NLRP3):c.2790A>C (p.Lys930Asn) rs876660975
NM_004895.4(NLRP3):c.2861C>T (p.Thr954Met) rs139814109
NM_004895.4(NLRP3):c.2895_2902delinsTTCCACACTTTC (p.Thr966fs) rs1553293315
NM_004895.4(NLRP3):c.2969G>C (p.Cys990Ser) rs876660974
NM_004895.4(NLRP3):c.298C>T (p.Arg100Cys) rs375013904
NM_004895.4(NLRP3):c.2993G>C (p.Cys998Ser) rs199517145
NM_004895.4(NLRP3):c.3043A>G (p.Lys1015Glu) rs771315000
NM_004895.4(NLRP3):c.342A>G (p.Glu114=) rs1064796501
NM_004895.4(NLRP3):c.392A>G (p.Lys131Arg) rs188623199
NM_004895.4(NLRP3):c.410G>A (p.Arg137His) rs138946894
NM_004895.4(NLRP3):c.420C>T (p.Tyr140=) rs1305478990
NM_004895.4(NLRP3):c.494A>G (p.Asn165Ser) rs199475733
NM_004895.4(NLRP3):c.508C>T (p.Arg170Ter)
NM_004895.4(NLRP3):c.523A>G (p.Lys175Glu) rs1041570007
NM_004895.4(NLRP3):c.584C>T (p.Thr195Met) rs76291085
NM_004895.4(NLRP3):c.598G>A (p.Val200Met) rs121908147
NM_004895.4(NLRP3):c.634G>A (p.Asp212Asn) rs372038150
NM_004895.4(NLRP3):c.644A>G (p.His215Arg) rs150396172
NM_004895.4(NLRP3):c.680C>T (p.Ala227Val) rs180177493
NM_004895.4(NLRP3):c.749A>G (p.Gln250Arg) rs876660971
NM_004895.4(NLRP3):c.766C>A (p.Leu256Met) rs1553286385
NM_004895.4(NLRP3):c.82C>T (p.His28Tyr) rs763551829
NM_004895.4(NLRP3):c.943A>G (p.Ile315Val) rs180177501
NM_004895.4(NLRP3):c.950C>T (p.Pro317Leu) rs180177462

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