ClinVar Miner

Submissions for variant NM_018896.5(CACNA1G):c.1633G>C (p.Ala545Pro)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003075145 SCV003461305 benign not provided 2023-07-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003075145 SCV004140838 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing CACNA1G: PP2, BS1

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