ClinVar Miner

Submissions for variant NC_000016.9:g.(?_3786017)_(3860800_?)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 RCV003113461 SCV003793729 pathogenic Rubinstein-Taybi syndrome 2022-02-01 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant disrupts a region of the CREBBP protein in which other variant(s) (p.Pro1494Ser) have been determined to be pathogenic (Invitae). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. This variant has not been reported in the literature in individuals affected with CREBBP-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 3-28 of the CREBBP gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame.

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