ClinVar Miner

Submissions for variant NM_000459.5(TEK):c.2228G>C (p.Gly743Ala)

dbSNP: rs202131936
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001515974 SCV001724167 benign not provided 2023-05-12 criteria provided, single submitter clinical testing
Mendelics RCV002248655 SCV002516695 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000424226 SCV000510516 likely pathogenic Acute myeloid leukemia 2016-05-13 no assertion criteria provided literature only

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