ClinVar Miner

Submissions for variant NM_000245.4(MET):c.1722C>T (p.Pro574=)

dbSNP: rs1562920359
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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 RCV002079709 SCV002423474 likely benign Renal cell carcinoma 2024-02-17 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247538 SCV005895232 benign Papillary renal cell carcinoma type 1 2024-11-08 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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