ClinVar Miner

Submissions for variant NM_001348323.3(TRIP12):c.4253G>A (p.Arg1418Lys)

gnomAD frequency: 0.00001  dbSNP: rs1157793506
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001333209 SCV001525727 uncertain significance Clark-Baraitser syndrome 2018-10-09 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Fulgent Genetics, Fulgent Genetics RCV001333209 SCV002788926 uncertain significance Clark-Baraitser syndrome 2022-03-22 criteria provided, single submitter 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.