ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.135-?_5193+?del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000196199 SCV000253905 pathogenic Hereditary breast ovarian cancer syndrome 2015-02-20 criteria provided, single submitter clinical testing This sequence change is a gross deletion of the genomic region encompassing exons 4-18 of the BRCA1 gene. This deletion extends to both edges of the assayed region, and the 5' and 3' boundaries of this event are not known. This deletion causes a translational frameshift and is expected to result in an absent or disrupted protein product While this particular variant has not been reported in the literature, truncating sequence changes in BRCA1 are known to be pathogenic (PMID: 20104584). For these reasons, this variant has been classified as Pathogenic.

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