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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 768833	NM_001146312.3(MYOCD):c.226G>A (p.Asp76Asn)	MYOCD (D76N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 779171	NM_001146312.3(MYOCD):c.423G>A (p.Gln141=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 707960	NM_001146312.3(MYOCD):c.1447G>A (p.Gly483Ser)	MYOCD (G483S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 713293	NM_001146312.3(MYOCD):c.1917G>A (p.Pro639=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 786432	NM_001146312.3(MYOCD):c.2118C>T (p.His706=)	MYOCD	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 780416	NM_001146312.3(MYOCD):c.2634C>T (p.Ser878=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 780417	NM_001146312.3(MYOCD):c.2721C>G (p.Gly907=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 780418	NM_001146312.3(MYOCD):c.2739G>A (p.Gln913=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

ClinVar