ClinVar Miner

Submissions for variant NM_015465.5(GEMIN5):c.3194C>T (p.Ala1065Val)

gnomAD frequency: 0.00706  dbSNP: rs115551140
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000954918 SCV001101585 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV002547257 SCV003603626 likely benign Inborn genetic diseases 2022-12-01 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.
CeGaT Center for Human Genetics Tuebingen RCV000954918 SCV005074401 benign not provided 2024-06-01 criteria provided, single submitter clinical testing GEMIN5: BP4, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000954918 SCV005226628 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.