ClinVar Miner

Submissions for variant NM_206965.2(FTCD):c.468C>T (p.Ala156=)

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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 RCV003104387 SCV003780831 uncertain significance Glutamate formiminotransferase deficiency 2024-10-17 criteria provided, single submitter clinical testing This sequence change affects codon 156 of the FTCD mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the FTCD protein. This variant is present in population databases (rs138762824, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with FTCD-related conditions. ClinVar contains an entry for this variant (Variation ID: 2413591). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a 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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