ClinVar Miner

Submissions for variant NM_003098.3(SNTA1):c.1426-1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003296664 SCV004000393 uncertain significance Cardiovascular phenotype 2023-03-23 criteria provided, single submitter clinical testing The c.1426-1G>A intronic variant results from a G to A substitution one nucleotide upstream from coding exon 8 of the SNTA1 gene. This nucleotide position is highly conserved in available vertebrate species. In silico splice site analysis predicts that this alteration will weaken the native splice acceptor site. Alterations that disrupt the canonical splice site are expected to cause aberrant splicing, resulting in an abnormal protein or a transcript that is subject to nonsense-mediated mRNA decay. However, the evidence for this gene-disease relationship is limited; therefore, the clinical significance of this alteration is unclear.

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