ClinVar Miner

Submissions for variant NM_001376013.1(EPB41):c.1187A>G (p.Tyr396Cys)

gnomAD frequency: 0.00010  dbSNP: rs201227668
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
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001332 SCV001158521 uncertain significance Elliptocytosis 1 2019-06-10 criteria provided, single submitter clinical testing
Ambry Genetics RCV002549160 SCV003526011 uncertain significance Inborn genetic diseases 2024-09-10 criteria provided, single submitter clinical testing The c.560A>G (p.Y187C) alteration is located in exon 9 (coding exon 6) of the EPB41 gene. This alteration results from a A to G substitution at nucleotide position 560, causing the tyrosine (Y) at amino acid position 187 to be replaced by a cysteine (C). 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.