ClinVar Miner

Submissions for variant NM_014009.4(FOXP3):c.816G>A (p.Val272=)

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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 RCV003625361 SCV004491364 uncertain significance Insulin-dependent diabetes mellitus secretory diarrhea syndrome 2023-04-13 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. Variants that disrupt 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. This variant has not been reported in the literature in individuals affected with FOXP3-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change affects codon 272 of the FOXP3 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the FOXP3 protein. This variant also falls at the last nucleotide of exon 8, which is part of the consensus splice site for this exon.

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