ClinVar Miner

Submissions for variant NM_007046.4(EMILIN1):c.1808C>T (p.Ser603Phe)

gnomAD frequency: 0.00001  dbSNP: rs534036052
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003370242 SCV004080860 uncertain significance Inborn genetic diseases 2023-08-08 criteria provided, single submitter clinical testing The c.1808C>T (p.S603F) alteration is located in exon 4 (coding exon 4) of the EMILIN1 gene. This alteration results from a C to T substitution at nucleotide position 1808, causing the serine (S) at amino acid position 603 to be replaced by a phenylalanine (F). 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.