ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2827A>G (p.Ile943Val) (rs786205757)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000170796 SCV000223351 uncertain significance not provided 2016-01-14 criteria provided, single submitter clinical testing p.Ile943Val (ATT>GTT): c.2827 A>G in exon 21 of the CACNA1C gene (NM_000719.6). The Ile943Val variant in the CACNA1C gene has not been reported as a disease-causing mutation or as a benign polymorphism to our knowledge. Although Ile943Val results in a conservative amino acid substitution, this occurs at a position that is highly conserved across species. However, there have been no nearby mutations reported in association with LQTS/Timothy syndrome, indicating this region of the protein may be tolerant of change. One in silico analysis program predicts Ile943Val is benign to the protein structure/function, while another predicts it is pathogenic. The Ile943Val variant was not observed in approximately 6000 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. In summary, with the clinical and molecular information available at this time, we cannot definitively determine if Ile943Val is a disease-causing mutation or a rare benign variant. The variant is found in LQT panel(s).

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