"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CASS4"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778896	NM_020356.4(CASS4):c.213C>T (p.Leu71=)	CASS4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 729002	NM_020356.4(CASS4):c.1232C>G (p.Ser411Cys)	CASS4 (S411C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 777599	NM_020356.4(CASS4):c.1277C>T (p.Ser426Leu)	CASS4 (S372L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 788688	NM_020356.4(CASS4):c.1472G>A (p.Arg491Lys)	CASS4 (R437K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 778178	NM_020356.4(CASS4):c.1583G>T (p.Arg528Leu)	CASS4 (R474L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 757485	NM_020356.4(CASS4):c.1806A>G (p.Pro602=)	CASS4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1374167	NC_000020.10:g.(?_54823900)_(57899514_?)del	ANKRD60, APCDD1L +36 more	Deletion	not provided	GUncertain significance

ClinVar