ClinVar Miner

Submissions for variant NM_003126.4(SPTA1):c.5020C>T (p.Leu1674Phe)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003740634 SCV004563789 uncertain significance not provided 2023-09-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003740634 SCV005832854 likely benign not provided 2024-09-21 criteria provided, single submitter clinical testing

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