List of variants in gene USH1C reported as likely benign for Usher syndrome, type 1C

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP
NM_153676.4(USH1C):c.*131G>C
NM_153676.4(USH1C):c.*405C>G	rs11827649
NM_153676.4(USH1C):c.*42C>T	rs16934270
NM_153676.4(USH1C):c.101A>G (p.His34Arg)	rs75157409
NM_153676.4(USH1C):c.1211-1129G>A	rs35188020
NM_153676.4(USH1C):c.2499C>T (p.Ile833=)	rs34581703
NM_153676.4(USH1C):c.648G>A (p.Leu216=)	rs77137413
NM_153676.4(USH1C):c.819+10G>C	rs41282936

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.