ClinVar Miner

Submissions for variant NM_001372044.2(SHANK3):c.2673G>C (p.Pro891=)

dbSNP: rs1569114751
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002312411 SCV000846759 likely benign Inborn genetic diseases 2016-06-01 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.
GeneDx RCV001566431 SCV001789944 likely benign not provided 2019-11-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001566431 SCV004155314 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing SHANK3: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV001566431 SCV005207861 likely benign not provided criteria provided, single submitter not provided

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.