ClinVar Miner

Submissions for variant NM_005585.5(SMAD6):c.1041_1042del (p.Ala348fs)

dbSNP: rs1894554671
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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 RCV001339178 SCV001532899 uncertain significance Aortic valve disease 2 2020-06-01 criteria provided, single submitter clinical testing Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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. This variant has not been reported in the literature in individuals with SMAD6-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change results in a frameshift in the SMAD6 gene (p.Ala348Glyfs*216). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 149 amino acids of the SMAD6 protein and extend the protein by an additional 66 amino acids.

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