ClinVar Miner

Submissions for variant NM_006642.5(SDCCAG8):c.1837A>G (p.Ile613Val)

dbSNP: rs2148018705
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001963605 SCV002254410 uncertain significance Senior-Loken syndrome 7; Bardet-Biedl syndrome 16 2020-12-22 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. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The valine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with SDCCAG8-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces isoleucine with valine at codon 613 of the SDCCAG8 protein (p.Ile613Val). The isoleucine residue is weakly conserved and there is a small physicochemical difference between isoleucine and valine.

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