ClinVar Miner

Submissions for variant NM_000391.4(TPP1):c.1076-1G>A

dbSNP: rs1554901731
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666279 SCV000790543 likely pathogenic Neuronal ceroid lipofuscinosis 2 2017-03-28 criteria provided, single submitter clinical testing
Invitae RCV001208874 SCV001380283 likely pathogenic not provided 2022-10-25 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 551267). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant has not been reported in the literature in individuals affected with TPP1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change affects an acceptor splice site in intron 8 of the TPP1 gene. It is expected to disrupt RNA splicing. Variants that disrupt the donor or acceptor splice site typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in TPP1 are known to be pathogenic (PMID: 10330339).

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