ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1014T>G (p.Asn338Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004944282 SCV005450858 uncertain significance Hereditary cancer-predisposing syndrome 2024-11-11 criteria provided, single submitter clinical testing The p.N338K variant (also known as c.1014T>G), located in coding exon 1 of the MET gene, results from a T to G substitution at nucleotide position 1014. The asparagine at codon 338 is replaced by lysine, an amino acid with 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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