ClinVar Miner

List of variants in gene NLRP3 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_001243133.2(NLRP3):c.476G>T (p.Ser159Ile)
NM_004895.4(NLRP3):c.1251C>T (p.Ile417=) rs139852370
NM_004895.4(NLRP3):c.1367G>A (p.Gly456Glu) rs199696688
NM_004895.4(NLRP3):c.1651T>C (p.Leu551=) rs144469697
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.2307C>G (p.Gly769=) rs150229101
NM_004895.4(NLRP3):c.2861C>T (p.Thr954Met) rs139814109
NM_004895.4(NLRP3):c.950C>T (p.Pro317Leu) rs180177462

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