ClinVar Miner

Submissions for variant NM_000245.4(MET):c.324A>C (p.Ser108=)

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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 RCV005150380 SCV005772071 likely benign Renal cell carcinoma 2024-05-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249787 SCV005899833 benign Papillary renal cell carcinoma type 1 2024-11-06 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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