ClinVar Miner

Submissions for variant NM_001372051.1(CASP8):c.1200_1201delinsTT (p.Leu400_Leu401=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003847744 SCV004643826 likely benign Autoimmune lymphoproliferative syndrome type 2B 2024-10-22 criteria provided, single submitter clinical testing

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