ClinVar Miner

Submissions for variant NM_005732.3(RAD50):c.3476-?_3618+?dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000240200 SCV000299151 likely pathogenic Hereditary cancer-predisposing syndrome 2016-03-10 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exon 23 of the RAD50 gene. While the exact position of the duplicated exon cannot be determined from this data, the duplicated copy of this region is likely in tandem and may result in an absent or disrupted protein product. This variant is not present in population databases and has not been reported in the literature in individuals with a RAD50-related disease. For these reasons, this variant has been classified as Likely Pathogenic.

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