"Revvity Omics, Revvity"[submitter] AND "APC2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2439142	NM_005883.3(APC2):c.2392_2395dup (p.Pro799fs)	APC2 (P798fs +1 more)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 2068732	NM_005883.3(APC2):c.3035G>A (p.Gly1012Asp)	APC2 (G1011D +1 more)	Single nucleotide variant (missense variant)	APC2-related disorder +3 more	GUncertain significance
Select item 2439144	NM_005883.3(APC2):c.4402C>T (p.Pro1468Ser)	APC2 (P1467S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 724709	NM_005883.3(APC2):c.4557G>A (p.Pro1519=)	APC2	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 2439143	NM_005883.3(APC2):c.4660G>C (p.Ala1554Pro)	APC2 (A1553P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 709496	NM_005883.3(APC2):c.4958G>A (p.Arg1653Gln)	APC2 (R1653Q +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2439145	NM_005883.3(APC2):c.5770C>A (p.Gln1924Lys)	LOC130062956, APC2 (Q1923K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2434404	NM_005883.3(APC2):c.6638_6640delinsCT (p.Glu2213fs)	APC2 (E2212fs +1 more)	Indel (frameshift variant)	not provided	GLikely pathogenic

ClinVar