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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUBN
(R2100*)
Insertion
(nonsense)
Imerslund-Grasbeck syndrome type 1
GPathogenic
CUBN
(E1900K)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 1
GUncertain significance
CUBN
(G1348*)
Single nucleotide variant
(nonsense)
Imerslund-Grasbeck syndrome type 1
GPathogenic
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