ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.1130-1G>T

dbSNP: rs769640244
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001236248 SCV001408964 uncertain significance Dyskeratosis congenita 2019-08-22 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. The current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in TINF2 cause disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with TINF2-related conditions. This variant is present in population databases (rs769640244, ExAC 0.006%). This sequence change affects an acceptor splice site in intron 7 of the TINF2 gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product.

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