ClinVar Miner

Submissions for variant NC_000020.10:g.(?_50400804)_(50401243_?)del

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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 RCV003109703 SCV003791696 likely pathogenic Duane-radial ray syndrome 2022-03-27 criteria provided, single submitter clinical testing In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. A similar copy number variant has been observed in individuals with Duane-radial ray syndrome (PMID: 15342710; Invitae). This variant is a gross deletion of the genomic region encompassing exon(s) 4 of the SALL4 gene, which includes the termination codon. This deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. While this deletion is not anticipated to lead to nonsense mediated decay, it is expected to alter mRNA translation or result in a truncated protein product.

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