ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2380-7T>G

dbSNP: rs2144384592
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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 RCV001976191 SCV002264823 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2022-08-16 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. ClinVar contains an entry for this variant (Variation ID: 1475376). This variant has not been reported in the literature in individuals affected with BRIP1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change falls in intron 16 of the BRIP1 gene. It does not directly change the encoded amino acid sequence of the BRIP1 protein.

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