ClinVar Miner

Submissions for variant NC_000006.11:g.72892502_72892503delinsCC

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001305692 SCV001495038 uncertain significance not provided 2020-01-30 criteria provided, single submitter clinical testing This sequence change replaces glutamine with proline at codon 443 of the RIMS1 protein (p.Gln443Pro). The glutamine residue is weakly conserved and there is a moderate physicochemical difference between glutamine and proline. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This variant has not been reported in the literature in individuals with RIMS1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: Not Available; PolyPhen-2: Benign; Align-GVGD: Not Available). 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.

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