C2713442[trait identifier] AND "deCODE genetics, Amgen"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2574095	NM_000038.6(APC):c.135+1G>A	APC	Single nucleotide variant (splice donor variant +1 more)	Familial adenomatous polyposis 1 +1 more	GLikely pathogenic
Select item 2574102	NM_000038.6(APC):c.2803dup (p.Tyr935fs)	APC (Y551fs +18 more)	Duplication (frameshift variant +1 more)	Familial adenomatous polyposis 1	GPathogenic
Select item 236589	NM_000038.6(APC):c.3340C>T (p.Arg1114Ter)	APC (R1096* +12 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic OLikely oncogenic
Select item 1070306	NM_000038.6(APC):c.3724C>T (p.Gln1242Ter)	APC (Q1082* +12 more)	Single nucleotide variant (nonsense)	Familial adenomatous polyposis 1	GPathogenic
Select item 2574109	NM_000038.6(APC):c.4667del (p.Thr1556fs)	APC (T1172fs +18 more)	Deletion (frameshift variant +1 more)	Familial adenomatous polyposis 1	GLikely pathogenic
Select item 2574116	NM_000038.6(APC):c.6474del (p.Phe2159fs)	APC (F1775fs +18 more)	Deletion (frameshift variant +1 more)	Familial adenomatous polyposis 1	GPathogenic
Select item 218007	NM_000038.6(APC):c.7511G>A (p.Trp2504Ter)	APC (W2486* +12 more)	Single nucleotide variant (nonsense)	Familial adenomatous polyposis 1 +1 more	GPathogenic/Likely pathogenic
Select item 1453360	NM_000038.6(APC):c.7927_7928del (p.Leu2643fs)	APC (L2360fs +12 more)	Microsatellite (frameshift variant)	Classic or attenuated familial adenomatous polyposis +3 more	GPathogenic/Likely pathogenic

ClinVar