ClinVar Miner

Submissions for variant NM_000355.4(TCN2):c.666C>T (p.Ala222=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003427222 SCV004154861 likely benign not provided 2022-07-01 criteria provided, single submitter clinical testing TCN2: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003598176 SCV004507212 likely benign Transcobalamin II deficiency 2023-09-07 criteria provided, single submitter clinical testing

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