ClinVar Miner

Submissions for variant NM_007298.3(BRCA1):c.787+970_787+973delinsGA (rs1555591287)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000657267 SCV000778998 pathogenic not provided 2016-11-23 criteria provided, single submitter clinical testing This combined deletion and insertion is denoted BRCA1 c.1757_1760delCTATinsGA at the cDNA level and p.Pro586ArgfsX21 (P586RfsX21) at the protein level. The normal sequence, with the bases that are deleted and inserted in braces, is GAAC[delCTAT][insGA]AAGC. The variant causes a frameshift which changes a Proline to an Arginine at codon 586, and creates a premature stop codon at position 21 of the new reading frame. Although this variant has not, to our knowledge, been reported in the literature, it is predicted to cause loss of normal protein function through either protein truncation or nonsense-mediated mRNA decay. We consider this variant to be pathogenic.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.