"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MTCL1"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 738588	NM_001395333.1(MTCL1):c.1872C>T (p.Phe624=)	MTCL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 716494	NM_001395333.1(MTCL1):c.2144T>A (p.Leu715Gln)	MTCL1 (L355Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 781395	NM_001395333.1(MTCL1):c.2340A>T (p.Glu780Asp)	MTCL1 (E420D +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 779029	NM_001395333.1(MTCL1):c.2635A>G (p.Met879Val)	MTCL1 (M519V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 777281	NM_001395333.1(MTCL1):c.3225G>A (p.Lys1075=)	MTCL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711698	NM_001395333.1(MTCL1):c.4602C>T (p.Cys1534=)	MTCL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 719546	NM_001395333.1(MTCL1):c.4843C>T (p.Arg1615Cys)	MTCL1 (R1255C +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar