ClinVar Miner

Submissions for variant NM_213599.2(ANO5):c.2520+6C>T (rs886042378)

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
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000327836 SCV000333722 uncertain significance not provided 2016-09-17 criteria provided, single submitter clinical testing
Invitae RCV000543918 SCV000645911 uncertain significance Gnathodiaphyseal dysplasia; Limb-girdle muscular dystrophy, type 2L 2016-10-08 criteria provided, single submitter clinical testing This sequence change falls in intron 21 of the ANO5 gene. It does not directly change the encoded amino acid sequence of the ANO5 protein. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a ANO5-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies. In summary, this is a novel intronic change with uncertain impact on splicing. Therefore, it has been classified as a Variant of 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.