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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUBN
(P3464A)
Single nucleotide variant
(missense variant)
Proteinuria, chronic benign
GUncertain significance
CUBN
(S1592fs)
Microsatellite
(frameshift variant)
Proteinuria, chronic benign
GPathogenic
CUBN
(Q1585*)
Single nucleotide variant
(nonsense)
Proteinuria, chronic benign
GPathogenic
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