ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.112-11T>A

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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 RCV003072336 SCV003466548 uncertain significance Costello syndrome 2022-04-19 criteria provided, single submitter clinical testing This sequence change falls in intron 2 of the HRAS gene. It does not directly change the encoded amino acid sequence of the HRAS protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with HRAS-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. 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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