ClinVar Miner

Submissions for variant NM_006642.5(SDCCAG8):c.1507A>G (p.Ser503Gly)

gnomAD frequency: 0.00001  dbSNP: rs778441055
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
Ambry Genetics RCV002684362 SCV003718011 uncertain significance Inborn genetic diseases 2022-08-12 criteria provided, single submitter clinical testing The c.1507A>G (p.S503G) alteration is located in exon 13 (coding exon 13) of the SDCCAG8 gene. This alteration results from a A to G substitution at nucleotide position 1507, causing the serine (S) at amino acid position 503 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Fulgent Genetics, Fulgent Genetics RCV005021762 SCV005651015 uncertain significance Senior-Loken syndrome 7; Bardet-Biedl syndrome 16 2024-04-22 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.