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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLE
(M1632V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
POLE
(E1409K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
POLE
(R1125*)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
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