ClinVar Miner

List of variants in gene NLRP3 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001243133.2(NLRP3):c.657C>T (p.Thr219=) rs7525979 0.10943
NM_001243133.2(NLRP3):c.1302C>T (p.Ser434=) rs34298354 0.08679
NM_001243133.2(NLRP3):c.2107C>A (p.Gln703Lys) rs35829419 0.03262
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met) rs121908147 0.00835
NM_001243133.2(NLRP3):c.423C>T (p.Tyr141=) rs56710146 0.00680
NM_001243133.2(NLRP3):c.1231C>T (p.Leu411=) rs148478875 0.00638
NM_001243133.2(NLRP3):c.1600C>T (p.Leu534=) rs116054301 0.00596
NM_001243133.2(NLRP3):c.1020C>T (p.Pro340=) rs41311573 0.00548
NM_001243133.2(NLRP3):c.1389C>T (p.His463=) rs111400208 0.00354
NM_001243133.2(NLRP3):c.1920C>T (p.Phe640=) rs34698071 0.00230
NM_001243133.2(NLRP3):c.2151-7T>C rs116546330 0.00084
NM_001243133.2(NLRP3):c.2488C>A (p.Leu830Ile) rs114158404 0.00083
NM_001243133.2(NLRP3):c.930C>T (p.Asp310=) rs143840033 0.00076
NM_001243133.2(NLRP3):c.3048A>C (p.Leu1016Phe) rs143548979 0.00068
NM_001243133.2(NLRP3):c.1639A>T (p.Ser547Cys) rs139833874 0.00061
NM_001243133.2(NLRP3):c.2855C>T (p.Thr952Met) rs139814109 0.00051
NM_001243133.2(NLRP3):c.2176A>G (p.Ser726Gly) rs147946775 0.00049
NM_001243133.2(NLRP3):c.203T>C (p.Met68Thr) rs147559626 0.00048
NM_001243133.2(NLRP3):c.1245C>T (p.Ile415=) rs139852370 0.00045
NM_001243133.2(NLRP3):c.1401C>T (p.Leu467=) rs141637807 0.00029
NM_001243133.2(NLRP3):c.674C>T (p.Ala225Val) rs180177493 0.00019
NM_001243133.2(NLRP3):c.2364C>A (p.Ile788=) rs766840708 0.00013
NM_001243133.2(NLRP3):c.906C>T (p.Phe302=) rs756989752 0.00011
NM_001243133.2(NLRP3):c.225G>A (p.Ala75=) rs140219362 0.00007
NM_001243133.2(NLRP3):c.207C>T (p.Ala69=) rs200082602 0.00005
NM_001243133.2(NLRP3):c.2424C>T (p.Leu808=) rs147154764 0.00005
NM_001243133.2(NLRP3):c.220G>A (p.Ala74Thr) rs537715421 0.00004
NM_001243133.2(NLRP3):c.476G>T (p.Ser159Ile) rs374170024 0.00004
NM_001243133.2(NLRP3):c.1669A>G (p.Thr557Ala) rs180177461 0.00003
NM_001243133.2(NLRP3):c.1269G>A (p.Gln423=) rs201035625 0.00002
NM_001243133.2(NLRP3):c.2732A>G (p.Asn911Ser) rs577683668 0.00002
NM_001243133.2(NLRP3):c.14G>A (p.Arg5His)
NM_001243133.2(NLRP3):c.154C>G (p.Leu52Val) rs1475761802
NM_001243133.2(NLRP3):c.1629C>T (p.Asn543=)
NM_001243133.2(NLRP3):c.1698C>T (p.Phe566=)
NM_001243133.2(NLRP3):c.1899C>T (p.Tyr633=) rs200089426
NM_001243133.2(NLRP3):c.1912G>A (p.Glu638Lys)
NM_001243133.2(NLRP3):c.2154G>T (p.Leu718Phe)
NM_001243133.2(NLRP3):c.2185C>A (p.Arg729=) rs148590318
NM_001243133.2(NLRP3):c.224C>T (p.Ala75Val) rs200288250
NM_001243133.2(NLRP3):c.2322-5T>C
NM_001243133.2(NLRP3):c.2337C>G (p.Gly779=)
NM_001243133.2(NLRP3):c.2575T>C (p.Tyr859His) rs2103174031
NM_001243133.2(NLRP3):c.2608G>A (p.Val870Ile)
NM_001243133.2(NLRP3):c.2752C>T (p.Arg918Ter)
NM_001243133.2(NLRP3):c.523C>T (p.His175Tyr) rs1662663283
NM_001243133.2(NLRP3):c.724_725delinsAA (p.Ala242Lys)
NM_001243133.2(NLRP3):c.726G>A (p.Ala242=) rs3806268

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.