ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.922G>T (p.Glu308Ter)

gnomAD frequency: 0.00001  dbSNP: rs1232383398
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001040031 SCV001203586 uncertain significance Dyskeratosis congenita 2023-11-07 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Glu308*) in the TINF2 gene. It is expected to result in an absent or disrupted protein product. However, the current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in TINF2 cause disease. This variant is present in population databases (no rsID available, gnomAD 0.004%). This variant has not been reported in the literature in individuals affected with TINF2-related conditions. ClinVar contains an entry for this variant (Variation ID: 838478). 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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