ClinVar Miner

Submissions for variant NM_000245.4(MET):c.2322A>G (p.Arg774=)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002450186 SCV002735064 likely benign Hereditary cancer-predisposing syndrome 2021-12-05 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV003763170 SCV004446917 likely benign Renal cell carcinoma 2022-11-14 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005248768 SCV005899353 benign Papillary renal cell carcinoma type 1 2024-11-11 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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