ClinVar Miner

Submissions for variant NC_000017.10:g.(?_59861625)_(59938906_?)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 RCV000535195 SCV000633522 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2017-02-18 criteria provided, single submitter clinical testing This variant is a gross duplication of the genomic region encompassing exons 2-11 of the BRIP1 gene. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. The 3' boundary is likely confined to intron 11 of the BRIP1 gene. This variant has not been reported in the literature in individuals with a BRIP1-related disease. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the duplicated amino acids is currently unknown. In summary, the exact genomic location of this variant is unknown and the impact of this duplication on BRIP1 protein function has not been established. Therefore, it has been classified as a Variant of Uncertain Significance.

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