ClinVar Miner

Submissions for variant NM_007298.3(BRCA1):c.787+1851_787+1852delinsAC (rs730881460)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159907 SCV000210024 uncertain significance not specified 2014-05-14 criteria provided, single submitter clinical testing This variant is denoted BRCA1 c.2638_2639delGAinsAC at the cDNA level, p.Glu880Thr (E880T) at the protein level. The normal sequence, with the bases that are deleted and inserted in brackets, is AGAA[delGAinsAC]GGAA. This in frame deletion and insertion, also denoted BRCA1 c.2757_2758delGAinsAC using alternate nomenclature, occurs on the same allele (in cis) and results in the missense change of a Glutamic Acid to a Threonine (GAG>ACG). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. Neither BRCA1 c.2638_2639delGAinsAC nor BRCA1 Glu880Thr (by this or an alternate nucleotide change) was observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Since Glutamic Acid and Threonine differ in some properties, this is considered a semi-conservative amino acid substitution. BRCA1 Glu880Thr occurs at a position that is variable across species and is located in the DNA binding domain (Narod 2004). In addition, in silico analyses are inconsistent regarding the effect this variant may have on protein structure and function. Based on currently available information, we consider BRCA1 Glu880Thr to be a variant of uncertain significance.

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