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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLRP3
(E343K +1 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GUncertain significance
NLRP3
(Q507R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
NLRP3
(Q600* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
NLRP3
(S726T +1 more)
Single nucleotide variant
(missense variant +1 more)
Cryopyrin associated periodic syndrome
+1 more
GUncertain significance
NLRP3
(N862H +3 more)
Single nucleotide variant
(missense variant)
Cryopyrin associated periodic syndrome
+1 more
GUncertain significance
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