U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUBN
Single nucleotide variant
(synonymous variant)
Imerslund-Grasbeck syndrome type 1
+2 more
GConflicting classifications of pathogenicity
CUBN
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CUBN
(V2990I)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CUBN
(R1695H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CUBN
(A1690V)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 1
+4 more
GConflicting classifications of pathogenicity
CUBN
(P1357A)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 1
+3 more
GUncertain significance
CUBN
(S865N)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CUBN
(T622fs)
Deletion
(frameshift variant)
Imerslund-Grasbeck syndrome type 1
+2 more
GPathogenic
CUBN
(D561N)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 1
+4 more
GConflicting classifications of pathogenicity
CUBN
(W502*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic/Likely pathogenic
CUBN
(S484G)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
CUBN, LOC129390143
Deletion
(nonsense)
not provided
GPathogenic
Format
Items per page
Sort by
Choose Destination