List of variants in gene TSEN54 reported as uncertain significance for anterior horn disorder

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

Total variants: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_207346.3(TSEN54):c.83C>T (p.Ser28Leu)	rs201089582	0.00116
NM_207346.3(TSEN54):c.1313G>A (p.Arg438Gln)	rs200228117	0.00041
NM_207346.3(TSEN54):c.1136G>A (p.Arg379Gln)	rs201948434	0.00038
NM_207346.3(TSEN54):c.622C>T (p.Arg208Trp)	rs147165460	0.00015
NM_207346.3(TSEN54):c.946C>T (p.Arg316Cys)	rs377207901	0.00014
NM_207346.3(TSEN54):c.1035G>C (p.Lys345Asn)	rs376308638	0.00007
NM_207346.3(TSEN54):c.637A>G (p.Lys213Glu)	rs184421010	0.00003
NM_207346.3(TSEN54):c.808C>T (p.Pro270Ser)	rs758853965	0.00002
NM_207346.3(TSEN54):c.1186C>T (p.Arg396Trp)	rs542013784	0.00001
NM_207346.3(TSEN54):c.1039_1041delinsTAC (p.Lys347Tyr)	rs1568003520
NM_207346.3(TSEN54):c.1280T>C (p.Leu427Pro)	rs2053450384
NM_207346.3(TSEN54):c.167G>A (p.Arg56His)	rs1281448557
NM_207346.3(TSEN54):c.175C>G (p.Arg59Gly)

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.