ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.1254dup (p.Cys419fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Biochemistry, Faculty of Medicine, University of Khartoum RCV002284296 SCV002573701 pathogenic Hereditary spastic paraplegia 15 criteria provided, single submitter research

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