ClinVar Miner

Submissions for variant NM_080746.3(RPL10L):c.94C>T (p.Arg32Cys)

gnomAD frequency: 0.00003  dbSNP: rs193920822
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 RCV004019791 SCV005015412 uncertain significance not specified 2023-11-28 criteria provided, single submitter clinical testing The c.94C>T (p.R32C) alteration is located in exon 1 (coding exon 1) of the RPL10L gene. This alteration results from a C to T substitution at nucleotide position 94, causing the arginine (R) at amino acid position 32 to be replaced by a cysteine (C). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Science for Life laboratory, Karolinska Institutet RCV000149333 SCV000088975 unknown Malignant tumor of prostate no assertion criteria provided not provided Converted during submission to Uncertain significance.

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.