C2713442[trait identifier] AND "Molecular Oncology Laboratory, Hospita - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 127847	NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val)	MUTYH (I223V +7 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +7 more	GUncertain significance
Select item 141368	NM_000038.6(APC):c.147_150del (p.Lys49fs)	APC (K59fs +2 more)	Deletion (frameshift variant +1 more)	Classic or attenuated familial adenomatous polyposis +5 more	GPathogenic OLikely oncogenic
Select item 230927	NM_000038.6(APC):c.266C>G (p.Ser89Ter)	APC (S89* +3 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 570563	NM_000038.6(APC):c.1240C>G (p.Arg414Gly)	APC (R396G +10 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 482253	NM_000038.6(APC):c.1966C>G (p.Leu656Val)	APC (L638V +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 127318	NM_000038.6(APC):c.7399C>A (p.Pro2467Thr)	APC (P2467T +12 more)	Single nucleotide variant (missense variant)	Familial adenomatous polyposis 1 +5 more	GConflicting classifications of pathogenicity
Select item 587354	NM_000038.6(APC):c.8501A>C (p.His2834Pro)	APC (H2816P +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

ClinVar