"ITMI"[submitter] AND "MET"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 135554	NM_000245.4(MET):c.-14-3314A>T	MET	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 135555	NM_000245.4(MET):c.-14-3297G>C	MET	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 134649	NM_000245.4(MET):c.71G>A (p.Gly24Glu)	MET (G24E)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 134646	NM_000245.4(MET):c.103A>T (p.Met35Leu)	MET (M35L)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 41610	NM_000245.4(MET):c.110T>C (p.Val37Ala)	MET (V37A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer +4 more	GBenign/Likely benign
Select item 93571	NM_000245.4(MET):c.289C>G (p.Pro97Ala)	MET (P97A)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +4 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 specified +4 more	GConflicting classifications of pathogenicity
Select item 134647	NM_000245.4(MET):c.510C>G (p.Ser170Arg)	MET (S170R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 41629	NM_000245.4(MET):c.948A>G (p.Ile316Met)	MET (I316M)	Single nucleotide variant (missense variant +1 more)	not specified +7 more	GBenign/Likely benign
Select item 132694	NM_000245.4(MET):c.1039G>A (p.Ala347Thr)	MET (A347T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 93565	NM_000245.4(MET):c.1085T>C (p.Met362Thr)	MET (M362T)	Single nucleotide variant (missense variant +1 more)	Papillary renal cell carcinoma type 1 +4 more	GBenign
Select item 41611	NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	MET (N375S)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign
Select item 134648	NM_000245.4(MET):c.1171G>A (p.Gly391Arg)	MET (G391R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +2 more	GUncertain significance
Select item 134652	NM_000245.4(MET):c.1660G>A (p.Gly554Arg)	MET (G554R +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +2 more	GConflicting classifications of pathogenicity
Select item 135556	NM_000245.4(MET):c.1701+25A>G	MET	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 135557	NM_000245.4(MET):c.1701+58_1701+59insTG	MET	Insertion (intron variant)	not specified	Gnot provided
Select item 135559	NM_000245.4(MET):c.1701+80dup	MET	Duplication (intron variant)	not specified	Gnot provided
Select item 135558	NM_000245.4(MET):c.1701+75T>G	MET	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 134653	NM_000245.4(MET):c.1723C>A (p.Leu575Ile)	MET (L575I +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 134654	NM_000245.4(MET):c.1771C>T (p.Arg591Trp)	MET (R591W +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 97 +4 more	GConflicting classifications of pathogenicity
Select item 135560	NM_000245.4(MET):c.1965+20A>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 134655	NM_000245.4(MET):c.1972G>A (p.Val658Ile)	MET (V658I +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +3 more	GConflicting classifications of pathogenicity
Select item 134642	NM_000245.4(MET):c.2548A>G (p.Ile850Val)	MET (I868V +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 134643	NM_000245.4(MET):c.2662C>T (p.His888Tyr)	MET (H906Y +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 41623	NM_000245.4(MET):c.2908C>T (p.Arg970Cys)	MET (R988C +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 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)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 134644	NM_000245.4(MET):c.2977A>G (p.Thr993Ala)	MET (T1011A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 134645	NM_000245.4(MET):c.3522T>C (p.His1174=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma +3 more	GBenign/Likely benign
Select item 134650	NM_000245.4(MET):c.3973G>A (p.Glu1325Lys)	MET (E1343K +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 134651	NM_000245.4(MET):c.4087G>A (p.Ala1363Thr)	MET (A1381T +2 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign

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Items: 30