"Neuberg Centre For Genomic Medicine, NCGM"[submitter] AND "POLE"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 654942	NM_006231.4(POLE):c.6496G>A (p.Asp2166Asn)	POLE (D2166N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 473789	NM_006231.4(POLE):c.6271C>T (p.Pro2091Ser)	POLE (P2091S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 420695	NM_006231.4(POLE):c.5215A>G (p.Ile1739Val)	POLE (I1739V)	Single nucleotide variant (missense variant)	Colorectal cancer, susceptibility to, 12 +2 more	GUncertain significance
Select item 863960	NM_006231.4(POLE):c.5036G>A (p.Arg1679His)	POLE (R1679H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1697427	NM_006231.4(POLE):c.626A>G (p.Lys209Arg)	POLE (K209R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 240443	NM_006231.4(POLE):c.274A>C (p.Ser92Arg)	POLE (S92R)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance

ClinVar