ClinVar Miner

Submissions for variant NM_001350162.2(TEX15):c.933C>G (p.Phe311Leu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003140967 SCV003827193 uncertain significance Spermatogenic failure 25 2021-05-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696314 SCV005195867 uncertain significance not provided criteria provided, single submitter not provided

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