ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3733T>G (p.Phe1245Val) (rs281864720)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000055895 SCV000086903 pathologic Neuroblastoma 3 2012-09-27 no assertion criteria provided curation Converted during submission to Pathogenic.
Database of Curated Mutations (DoCM) RCV000426209 SCV000503774 pathogenic Neuroblastoma 2014-10-02 no assertion criteria provided literature only

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