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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUTYH
(G382D +8 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+8 more
GPathogenic/Likely pathogenic
MUTYH
(R245H +8 more)
Single nucleotide variant
(missense variant +1 more)
MUTYH-related condition
+7 more
GPathogenic/Likely pathogenic
APC
(T270I +6 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
APC
(R1770H +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+8 more
GConflicting classifications of pathogenicity
TP53
(R151C +3 more)
Single nucleotide variant
(missense variant)
Li-Fraumeni syndrome
GLikely benign
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