ClinVar Miner

List of variants in gene NLRP3 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001243133.2(NLRP3):c.592G>A (p.Val198Met) rs121908147 0.00835
NM_001243133.2(NLRP3):c.1463G>A (p.Arg488Lys) rs145268073 0.00070
NM_001243133.2(NLRP3):c.2855C>T (p.Thr952Met) rs139814109 0.00051
NM_001243133.2(NLRP3):c.208G>A (p.Val70Met) rs117287351 0.00031
NM_001243133.2(NLRP3):c.2668G>T (p.Val890Leu) rs193085132 0.00025
NM_001243133.2(NLRP3):c.937A>G (p.Ile313Val) rs180177501 0.00025
NM_001243133.2(NLRP3):c.2987G>C (p.Cys996Ser) rs199517145 0.00006
NM_001243133.2(NLRP3):c.-72G>A rs200386207 0.00003
NM_001243133.2(NLRP3):c.269C>T (p.Pro90Leu) rs145774400 0.00003
NM_001243133.2(NLRP3):c.2336G>A (p.Gly779Asp) rs768252357 0.00002
NM_001243133.2(NLRP3):c.431G>A (p.Ser144Asn) rs768059813 0.00001
NM_001243133.2(NLRP3):c.1535G>A (p.Cys512Tyr)
NM_001243133.2(NLRP3):c.3091G>C (p.Glu1031Gln) rs1572239975
NM_001243133.2(NLRP3):c.424G>A (p.Val142Met)
NM_001243133.2(NLRP3):c.578C>T (p.Thr193Met) rs76291085

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