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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 756077	NM_001025101.2(MBP):c.888C>T (p.Arg296=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 737907	NM_001025101.2(MBP):c.877A>C (p.Arg293=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 756700	NM_001025101.2(MBP):c.867G>A (p.Lys289=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 758882	NM_001025101.2(MBP):c.750+9C>T	LOC126862812, MBP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 778777	NM_001025101.2(MBP):c.657C>T (p.Pro219=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768944	NM_001025101.2(MBP):c.601G>A (p.Ala201Thr)	MBP (A68T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 743095	NM_001025101.2(MBP):c.507G>A (p.Thr169=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 742236	NM_001025101.2(MBP):c.391C>T (p.Leu131=)	MBP	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 728242	NM_001025101.2(MBP):c.243C>T (p.His81=)	MBP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar