ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.2792-6T>G

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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 RCV002999834 SCV003306959 uncertain significance RASopathy 2022-03-30 criteria provided, single submitter clinical testing This sequence change falls in intron 17 of the SOS1 gene. It does not directly change the encoded amino acid sequence of the SOS1 protein. 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. 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 SOS1-related conditions. This variant is not present in population databases (gnomAD no frequency).

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