ClinVar Miner

Submissions for variant NM_003632.3(CNTNAP1):c.74G>T (p.Cys25Phe)

dbSNP: rs2143644450
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratoire de Génétique Moléculaire, CHU Bordeaux RCV002280068 SCV002568823 likely pathogenic not provided criteria provided, single submitter clinical testing

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