ClinVar Miner

Submissions for variant NM_001081.3(CUBN):c.4921del (p.Tyr1641fs) (rs1564443979)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare	RCV000735732	SCV000863885	likely pathogenic	Megaloblastic anemia due to inborn errors of metabolism	2018-05-22	no assertion criteria provided	clinical testing

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