ClinVar Miner

Submissions for variant NC_000010.10:g.(?_98399836)_(98405338_?)dup

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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 RCV000558494 SCV000654984 uncertain significance Infantile spasms 2020-01-27 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. This duplication has not been reported in the literature in individuals with PIK3AP1-related disease. This variant is a gross duplication of the genomic region encompassing most of exon 8 of the PIK3AP1 gene, including the exon 8-intron 8 boundary (c.1267_1375+5394dup). The duplicated copy of this region is in tandem and the effect of this variant on RNA splicing and protein translation is unknown.

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