ClinVar Miner

Submissions for variant NC_000008.11:g.(?_100162261)_(100162440_?)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 RCV000540899 SCV000654659 pathogenic Primary ciliary dyskinesia 28 2019-07-09 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon 2 of the SPAG1 gene, which includes the initiator codon. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass the non-coding exon 1 and/or additional genes. The 3' boundary is likely confined to intron 2 of the SPAG1 gene. This is expected to result in an absent or disrupted protein product. Loss-of-function variants in SPAG1 are known to be pathogenic. A deletion that includes the non-coding exon 1 and exon 2 has been reported in individuals affected with primary ciliary dyskinesia (PMID: 27637300, 24055112). For these reasons, this variant has been classified as Pathogenic.

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