"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 486746	NM_000038.6(APC):c.1435T>A (p.Leu479Met)	APC (L461M +12 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 819844	NM_000038.6(APC):c.1703G>T (p.Ser568Ile)	APC (S442I +12 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 816	NM_000038.6(APC):c.3927_3931del (p.Glu1309fs)	APC (E1149fs +12 more)	Microsatellite (frameshift variant)	Familial adenomatous polyposis 1	GPathogenic FDA Recognized database
Select item 374105	NM_000038.6(APC):c.4901del (p.Pro1634fs)	APC (P1351fs +12 more)	Deletion (frameshift variant)	Familial adenomatous polyposis 1 +2 more	GPathogenic
Select item 161205	NM_000038.6(APC):c.7778A>G (p.Asn2593Ser)	APC (N2575S +12 more)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GConflicting classifications of pathogenicity
Select item 997683	NM_000038.5:c.1465_1466insSVA	APC	Insertion	Familial adenomatous polyposis 1	GPathogenic

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