ClinVar Miner

Submissions for variant NM_001036.6(RYR3):c.1788+4G>A

gnomAD frequency: 0.00002  dbSNP: rs1248271851
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001072010 SCV001237352 uncertain significance Epileptic encephalopathy 2019-12-30 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Experimental studies and prediction algorithms are not available or were not evaluated, and the effect of this variant on mRNA splicing is currently unknown. This variant has not been reported in the literature in individuals with RYR3-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 16 of the RYR3 gene. It does not directly change the encoded amino acid sequence of the RYR3 protein, but it affects a nucleotide within the consensus splice site of the intron.

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