"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41627	NM_000245.4(MET):c.504G>T (p.Glu168Asp)	MET (E168D)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 41611	NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	MET (N375S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 411912	NM_000245.4(MET):c.2318C>T (p.Pro773Leu)	MET (P791L +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 41623	NM_000245.4(MET):c.2908C>T (p.Arg970Cys)	MET (R988C +2 more)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 41624	NM_000245.4(MET):c.2975C>T (p.Thr992Ile)	MET (T1010I +2 more)	Single nucleotide variant (missense variant)	not specified +7 more	GConflicting classifications of pathogenicity
Select item 358693	NM_000245.4(MET):c.3523-12C>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma +4 more	GBenign/Likely benign
Select item 13883	NM_000245.4(MET):c.3658G>A (p.Val1220Ile)	MET (V1238I +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +1 more	GPathogenic/Likely pathogenic
Select item 1208570	NM_000245.4(MET):c.3936-13_3936-10del	MET	Microsatellite (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity