List of variants in gene ANO10 reported by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln)	rs3772165	0.59837
NM_018075.5(ANO10):c.1293+9A>G	rs7616708	0.56196
NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly)	rs56389778	0.05750
NM_018075.5(ANO10):c.1682C>T (p.Thr561Met)	rs17409162	0.04825
NM_018075.5(ANO10):c.788G>A (p.Arg263His)	rs41289586	0.01896
NM_018075.5(ANO10):c.980A>G (p.Tyr327Cys)	rs146569520	0.00359
NM_018075.5(ANO10):c.1219-23dup	rs367784953

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.