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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 753985	NM_024769.5(CLMP):c.1032A>G (p.Glu344=)	CLMP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 787547	NM_024769.5(CLMP):c.1011G>A (p.Gly337=)	CLMP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791496	NM_024769.5(CLMP):c.888C>T (p.Ser296=)	CLMP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 784224	NM_024769.5(CLMP):c.453G>A (p.Leu151=)	CLMP, LOC112042785	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1069033	NM_024769.5(CLMP):c.421G>T (p.Gly141Ter)	CLMP, LOC112042785 (G141*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 717942	NM_024769.5(CLMP):c.408G>A (p.Lys136=)	LOC112042785, CLMP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 719365	NM_024769.5(CLMP):c.163G>A (p.Asp55Asn)	CLMP (D55N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 717448	NM_024769.5(CLMP):c.48C>G (p.Thr16=)	CLMP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar