ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.215C>A (p.Ala72Asp) (rs121918454)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000441142 SCV000507240 likely pathogenic Neuroblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420417 SCV000507241 likely pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430256 SCV000507242 likely pathogenic Chronic lymphocytic leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440942 SCV000507243 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only

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