ClinVar Miner

List of variants in gene NLRP3 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP
NM_004895.4(NLRP3):c.*177delC rs796764638
NM_004895.4(NLRP3):c.*230G>C rs10754558
NM_004895.4(NLRP3):c.*324_*327delGTCT rs886506882
NM_004895.4(NLRP3):c.*328_*331delAACT rs1057515460
NM_004895.4(NLRP3):c.*351dupT rs397821684
NM_004895.4(NLRP3):c.*396T>A rs10802501
NM_004895.4(NLRP3):c.*489C>T rs10802502
NM_004895.4(NLRP3):c.*604A>C rs1057515532
NM_004895.4(NLRP3):c.-116T>C rs202234129
NM_004895.4(NLRP3):c.-197G>A rs1042817230
NM_004895.4(NLRP3):c.-225G>A rs138900557
NM_004895.4(NLRP3):c.-34G>T rs73136263
NM_004895.4(NLRP3):c.-405T>C rs7523422
NM_004895.4(NLRP3):c.-454G>A rs199475727
NM_004895.4(NLRP3):c.-476dupT rs144128307
NM_004895.4(NLRP3):c.-527C>G rs141994679
NM_004895.4(NLRP3):c.-527C>T rs141994679
NM_004895.4(NLRP3):c.-537A>T rs116502550
NM_004895.4(NLRP3):c.-555T>G rs72771992
NM_004895.4(NLRP3):c.-623C>T rs200090360
NM_004895.4(NLRP3):c.-62C>T rs201758466
NM_004895.4(NLRP3):c.-679G>A rs768557674
NM_004895.4(NLRP3):c.-68G>A rs202076321
NM_004895.4(NLRP3):c.-704C>T rs199723383
NM_004895.4(NLRP3):c.1038G>A (p.Leu346=) rs180177471
NM_004895.4(NLRP3):c.1049C>T (p.Thr350Met) rs151344629
NM_004895.4(NLRP3):c.1050G>A (p.Thr350=) rs143140947
NM_004895.4(NLRP3):c.1061C>T (p.Ala354Val) rs121908149
NM_004895.4(NLRP3):c.1064T>C (p.Leu355Pro) rs28937896
NM_004895.4(NLRP3):c.1125G>A (p.Glu375=) rs138613962
NM_004895.4(NLRP3):c.1237C>T (p.Leu413=) rs148478875
NM_004895.4(NLRP3):c.1251C>T (p.Ile417=) rs139852370
NM_004895.4(NLRP3):c.1308C>T (p.Ser436=) rs34298354
NM_004895.4(NLRP3):c.1367G>A (p.Gly456Glu) rs199696688
NM_004895.4(NLRP3):c.1380C>T (p.His460=) rs180177481
NM_004895.4(NLRP3):c.1395C>T (p.His465=) rs111400208
NM_004895.4(NLRP3):c.1590C>T (p.Ala530=) rs201644343
NM_004895.4(NLRP3):c.1606C>T (p.Leu536=) rs116054301
NM_004895.4(NLRP3):c.1645A>T (p.Ser549Cys) rs139833874
NM_004895.4(NLRP3):c.1651T>C (p.Leu551=) rs144469697
NM_004895.4(NLRP3):c.1711G>C (p.Gly571Arg) rs121908151
NM_004895.4(NLRP3):c.1820A>T (p.Glu607Val)
NM_004895.4(NLRP3):c.1926C>T (p.Phe642=) rs34698071
NM_004895.4(NLRP3):c.200C>G (p.Ala67Gly) rs763252989
NM_004895.4(NLRP3):c.209T>C (p.Met70Thr) rs147559626
NM_004895.4(NLRP3):c.2104G>A (p.Asp702Asn) rs781561828
NM_004895.4(NLRP3):c.2113C>A (p.Gln705Lys) rs35829419
NM_004895.4(NLRP3):c.2124C>T (p.Leu708=) rs149493236
NM_004895.4(NLRP3):c.2126C>A (p.Pro709Gln)
NM_004895.4(NLRP3):c.213C>T (p.Ala71=) rs200082602
NM_004895.4(NLRP3):c.214G>A (p.Val72Met) rs117287351
NM_004895.4(NLRP3):c.2182A>G (p.Ser728Gly) rs147946775
NM_004895.4(NLRP3):c.2191C>A (p.Arg731=) rs148590318
NM_004895.4(NLRP3):c.2220C>T (p.Ser740=) rs183128734
NM_004895.4(NLRP3):c.2307C>G (p.Gly769=) rs150229101
NM_004895.4(NLRP3):c.2430C>T (p.Leu810=) rs147154764
NM_004895.4(NLRP3):c.2638A>G (p.Lys880Glu) rs1057515488
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.283+11G>A rs577522959
NM_004895.4(NLRP3):c.2861C>T (p.Thr954Met) rs139814109
NM_004895.4(NLRP3):c.3048T>C (p.Ser1016=) rs1057515489
NM_004895.4(NLRP3):c.34A>C (p.Arg12=) rs1057515531
NM_004895.4(NLRP3):c.403+7G>A rs192297357
NM_004895.4(NLRP3):c.404-5C>T rs200459664
NM_004895.4(NLRP3):c.429C>T (p.Tyr143=) rs56710146
NM_004895.4(NLRP3):c.593G>A (p.Ser198Asn) rs180177459
NM_004895.4(NLRP3):c.598G>A (p.Val200Met) rs121908147
NM_004895.4(NLRP3):c.663C>T (p.Thr221=) rs7525979
NM_004895.4(NLRP3):c.732G>A (p.Ala244=) rs3806268
NM_004895.4(NLRP3):c.749A>G (p.Gln250Arg) rs876660971
NM_004895.4(NLRP3):c.784C>T (p.Arg262Trp) rs121908150
NM_004895.4(NLRP3):c.913G>A (p.Asp305Asn) rs121908153
NM_004895.4(NLRP3):c.950C>T (p.Pro317Leu) rs180177462

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