ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.117G>A (p.Lys39=)

dbSNP: rs956797047
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001340059 SCV001533849 uncertain significance Amelocerebrohypohidrotic syndrome 2020-10-14 criteria provided, single submitter clinical testing This sequence change affects codon 39 of the ROGDI mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the ROGDI protein. This variant also falls at the last nucleotide of exon 2 of the ROGDI coding sequence, which is part of the consensus splice site for this exon. 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). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with ROGDI-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database.

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