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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLE
(A2239V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
POLE
(R1286H)
Single nucleotide variant
(missense variant)
Colorectal cancer, susceptibility to, 12
+2 more
GUncertain significance
POLE
(M66I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
POLE
(F48fs)
Deletion
(frameshift variant)
not provided
GPathogenic
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