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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(K59fs +2 more)
Deletion
(frameshift variant +1 more)
not provided
+4 more
GPathogenic
APC
(S89* +3 more)
Single nucleotide variant
(nonsense +1 more)
Familial adenomatous polyposis 1
+1 more
GPathogenic
APC
(R396G +10 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GUncertain significance
APC
(L638V +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
APC
(P2467T +12 more)
Single nucleotide variant
(missense variant)
Colorectal cancer
+4 more
GConflicting classifications of pathogenicity
APC
(H2816P +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
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