"Institute for Clinical Genetics, University Hospital TU Dresden, Univ - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1319318	NM_000245.4(MET):c.34C>A (p.Leu12Ile)	MET (L12I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 142059	NM_000245.4(MET):c.406G>A (p.Val136Ile)	MET (V136I)	Single nucleotide variant (missense variant +1 more)	not specified +9 more	GConflicting classifications of pathogenicity
Select item 41627	NM_000245.4(MET):c.504G>T (p.Glu168Asp)	MET (E168D)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 1319317	NM_000245.4(MET):c.589G>A (p.Val197Ile)	MET (V197I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 485734	NM_000245.4(MET):c.818C>A (p.Thr273Asn)	MET (T273N)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 41630	NM_000245.4(MET):c.967A>G (p.Ser323Gly)	MET (S323G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 132694	NM_000245.4(MET):c.1039G>A (p.Ala347Thr)	MET (A347T)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +7 more	GConflicting classifications of pathogenicity
Select item 142899	NM_000245.4(MET):c.1051C>G (p.Pro351Ala)	MET (P351A)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +3 more	GUncertain significance
Select item 93564	NM_000245.4(MET):c.1076G>A (p.Arg359Gln)	MET (R359Q)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 584713	NM_000245.4(MET):c.1640G>A (p.Arg547Gln)	MET (R547Q +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 524880	NM_000245.4(MET):c.1862C>T (p.Thr621Ile)	MET (T621I +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 660201	NM_000245.4(MET):c.1912A>T (p.Ile638Leu)	MET (I208L +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GUncertain significance
Select item 188285	NM_000245.4(MET):c.1984A>G (p.Ile662Val)	MET (I662V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 1319489	NM_000245.4(MET):c.2392A>T (p.Ile798Leu)	MET (I368L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 216506	NM_000245.4(MET):c.3236A>G (p.His1079Arg)	MET (H1097R +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity
Select item 524890	NM_000245.4(MET):c.3601G>A (p.Val1201Ile)	MET (V1219I +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 184563	NM_000245.4(MET):c.3798+5T>C	MET	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity