ClinVar Miner

Submissions for variant NM_001127208.3(TET2):c.1712G>A (p.Arg571His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003333549 SCV004041213 uncertain significance Immunodeficiency 75 2023-01-09 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003436018 SCV004148637 uncertain significance not provided 2022-05-01 criteria provided, single submitter clinical testing TET2: PM2, BP4

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