ClinVar Miner

Submissions for variant NC_000007.13:g.(?_95951234)_(95951268_?)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 RCV004583529 SCV005064636 pathogenic Citrin deficiency 2023-07-04 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant is a gross deletion of the genomic region encompassing exon(s) 1 of the SLC25A13 gene, which includes the initiator codon. This deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SLC25A13 are known to be pathogenic (PMID: 10369257, 14680984, 27405544). A similar copy number variant has been observed in individual(s) with SLC25A13-related conditions (PMID: 29152073).

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