ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.2741C>T (p.Pro914Leu)

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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 RCV003817484 SCV004618769 likely benign not provided 2024-09-04 criteria provided, single submitter clinical testing

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