ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.261G>A (p.Lys87=)

gnomAD frequency: 0.00001  dbSNP: rs372668612
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001084544 SCV000623280 likely benign Bloom syndrome 2024-01-24 criteria provided, single submitter clinical testing
Ambry Genetics RCV000576007 SCV000672943 likely benign Hereditary cancer-predisposing syndrome 2017-05-15 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Eurofins Ntd Llc (ga) RCV000728499 SCV000856079 uncertain significance not provided 2017-08-18 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000576007 SCV002529437 likely benign Hereditary cancer-predisposing syndrome 2020-11-11 criteria provided, single submitter curation
Natera, Inc. RCV001084544 SCV001456634 likely benign Bloom syndrome 2020-09-16 no assertion criteria provided clinical testing

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.