"Athena Diagnostics Inc"[submitter] AND "MET"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 93567	NM_000245.4(MET):c.144G>A (p.Ala48=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 93578	NM_000245.4(MET):c.534C>T (p.Ser178=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GBenign
Select item 41611	NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	MET (N375S)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GBenign
Select item 93566	NM_000245.4(MET):c.1131C>T (p.Ile377=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma +4 more	GBenign
Select item 524856	NM_000245.4(MET):c.1477G>C (p.Glu493Gln)	MET (E493Q +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 41624	NM_000245.4(MET):c.2975C>T (p.Thr992Ile)	MET (T1010I +2 more)	Single nucleotide variant (missense variant)	Classic Hodgkin lymphoma +7 more	GConflicting classifications of pathogenicity

ClinVar