ClinVar Miner

Submissions for variant NM_006642.5(SDCCAG8):c.62_64dup (p.Leu21_Arg22insLeu)

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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 RCV003029831 SCV003332578 uncertain significance Senior-Loken syndrome 7; Bardet-Biedl syndrome 16 2022-03-18 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 affected with SDCCAG8-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.62_64dup, results in the insertion of 1 amino acid(s) of the SDCCAG8 protein (p.Leu21dup), but otherwise preserves the integrity of the reading frame.

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