ClinVar Miner

Submissions for variant NM_002107.6(H3-3A):c.100G>C (p.Gly34Arg) (rs1057519902)

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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) RCV000444419 SCV000506462 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426050 SCV000506463 likely pathogenic Adrenocortical carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436272 SCV000506464 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418626 SCV000506465 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only

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