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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(I1307K +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity; association; risk factor
APC
(E1149fs +12 more)
Microsatellite
(frameshift variant)
Familial adenomatous polyposis 1
GPathogenic
APC
(E1317Q +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+4 more
GBenign/Likely benign
APC
(V1804D +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GBenign
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