ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1399G>T (p.Val467Phe)

dbSNP: rs1004264326
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001894460 SCV002119288 uncertain significance Renal cell carcinoma 2020-12-23 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with MET-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with phenylalanine at codon 467 of the MET protein (p.Val467Phe). The valine residue is weakly conserved and there is a small physicochemical difference between valine and phenylalanine.
Ambry Genetics RCV004945738 SCV005447583 uncertain significance Hereditary cancer-predisposing syndrome 2024-07-07 criteria provided, single submitter clinical testing The p.V467F variant (also known as c.1399G>T), located in coding exon 3 of the MET gene, results from a G to T substitution at nucleotide position 1399. The valine at codon 467 is replaced by phenylalanine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the available evidence, the clinical significance of this variant remains unclear.

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