ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.789G>A (p.Leu263=)

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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 RCV003618144 SCV004378953 uncertain significance Pitt-Hopkins syndrome 2023-11-03 criteria provided, single submitter clinical testing This sequence change affects codon 263 of the TCF4 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the TCF4 protein. This variant also falls at the last nucleotide of exon 10, which is part of the consensus splice site for this exon. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with TCF4-related conditions. 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. 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.

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