ClinVar Miner

Submissions for variant NM_003200.5(TCF3):c.759_760del (p.Ser253fs)

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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 RCV003553379 SCV004270536 pathogenic not provided 2024-08-14 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ser253Argfs*95) in the TCF3 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in TCF3 are known to be pathogenic (PMID: 24216514, 30063982, 37277074). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with TCF3-related conditions. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. For these reasons, this variant has been classified as Pathogenic.

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