ClinVar Miner

Submissions for variant NM_004364.5(CEBPA):c.459G>A (p.Pro153=)

gnomAD frequency: 0.00001  dbSNP: rs779373951
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000535075 SCV000627097 benign Acute myeloid leukemia 2023-11-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257788 SCV002531752 likely benign Hereditary cancer-predisposing syndrome 2021-11-03 criteria provided, single submitter curation

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