ClinVar Miner

Submissions for variant NM_006888.6(CALM1):c.78C>T (p.Gly26=)

dbSNP: rs1555365884
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000540449 SCV000655578 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 4; Long QT syndrome 14 2017-01-19 criteria provided, single submitter clinical testing Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may alter RNA splicing, but this prediction has not been confirmed by published transcriptional studies. In summary, this is a novel silent change with uncertain impact on splicing. It has been classified as a Variant of Uncertain Significance. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a CALM1-related disease. This sequence change affects codon 26 of the CALM1 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the CALM1 protein.

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