ClinVar Miner

Submissions for variant NM_172240.3(POC1B):c.950T>C (p.Leu317Ser)

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
Fulgent Genetics, Fulgent Genetics RCV005011710 SCV005632103 uncertain significance Cone-rod dystrophy 20 2024-04-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV005392933 SCV006050955 uncertain significance Inborn genetic diseases 2025-02-06 criteria provided, single submitter clinical testing The c.950T>C (p.L317S) alteration is located in exon 9 (coding exon 9) of the POC1B gene. This alteration results from a T to C substitution at nucleotide position 950, causing the leucine (L) at amino acid position 317 to be replaced by a serine (S). 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.