ClinVar Miner

Submissions for variant NM_015409.5(EP400):c.970A>G (p.Arg324Gly)

gnomAD frequency: 0.00086  dbSNP: rs541534183
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000948909 SCV001095136 likely benign not provided 2018-05-16 criteria provided, single submitter clinical testing
Ambry Genetics RCV004029794 SCV003746083 uncertain significance not specified 2022-08-02 criteria provided, single submitter clinical testing The c.970A>G (p.R324G) alteration is located in exon 2 (coding exon 1) of the EP400 gene. This alteration results from a A to G substitution at nucleotide position 970, causing the arginine (R) at amino acid position 324 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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.