ClinVar Miner

Submissions for variant NM_014714.4(IFT140):c.4341del (p.Arg1448fs)

dbSNP: rs1209319873
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001362672 SCV001558702 uncertain significance Saldino-Mainzer syndrome 2021-06-13 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals with IFT140-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change results in a frameshift in the IFT140 gene (p.Arg1448Glyfs*90). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 16 amino acids of the IFT140 protein and extend the protein by an additional 74 amino acids.

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