ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.682-13A>T

dbSNP: rs81002888
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000781087 SCV000918899 uncertain significance not specified 2018-04-23 criteria provided, single submitter clinical testing Variant summary: BRCA2 c.682-13A>T alters a non-conserved nucleotide located close to a canonical splice site and therefore could affect mRNA splicing, leading to a significantly altered protein sequence. 5/5 computational tools predict no significant impact on normal splicing. However, these predictions have yet to be confirmed by functional studies. The variant was absent in 74986 control chromosomes. The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. To our knowledge, no occurrence of c.682-13A>T in individuals affected with Hereditary Breast and Ovarian Cancer and no experimental evidence demonstrating its impact on protein function have been reported. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as VUS-possibly benign.
Color Diagnostics, LLC DBA Color Health RCV001188241 SCV001355262 likely benign Hereditary cancer-predisposing syndrome 2020-01-28 criteria provided, single submitter clinical testing
Invitae RCV002067376 SCV002479900 likely benign Hereditary breast ovarian cancer syndrome 2023-03-26 criteria provided, single submitter clinical testing

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