ClinVar Miner

Submissions for variant NM_003126.4(SPTA1):c.790G>C (p.Ala264Pro)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV003481540 SCV004224689 uncertain significance not provided 2022-12-30 criteria provided, single submitter clinical testing PM2
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003481540 SCV004563666 uncertain significance not provided 2023-09-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003481540 SCV005847428 likely benign not provided 2024-09-10 criteria provided, single submitter clinical testing

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