"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CEACAM3 - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 769003	NM_001815.5(CEACAM3):c.229A>C (p.Ser77Arg)	CEACAM3 (S77R)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 769004	NM_001815.5(CEACAM3):c.233T>A (p.Leu78Gln)	CEACAM3 (L78Q)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 769005	NM_001815.5(CEACAM3):c.248T>C (p.Val83Ala)	CEACAM3 (V83A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 769006	NM_001815.5(CEACAM3):c.277G>C (p.Ala93Pro)	CEACAM3 (A93P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 769007	NM_001815.5(CEACAM3):c.283T>A (p.Tyr95Asn)	CEACAM3 (Y95N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 777493	NM_001815.5(CEACAM3):c.309C>A (p.Thr103=)	CEACAM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 771930	NM_001815.5(CEACAM3):c.333T>C (p.Asn111=)	CEACAM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 769008	NM_001815.5(CEACAM3):c.398A>G (p.Glu133Gly)	CEACAM3 (E133G)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 769009	NM_001815.5(CEACAM3):c.405T>C (p.Thr135=)	CEACAM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2423350	NC_000019.9:g.(?_39904727)_(42931301_?)dup	ACTMAP, AKT2 +84 more	Duplication	MEGF8-related Carpenter syndrome +3 more	GUncertain significance