List of variants in gene TSEN2 reported as uncertain significance for not specified

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025265.4(TSEN2):c.376C>T (p.Arg126Cys)	rs151133206	0.00069
NM_025265.4(TSEN2):c.587G>T (p.Gly196Val)	rs143243952	0.00022
NM_025265.4(TSEN2):c.872A>G (p.Tyr291Cys)	rs140979604	0.00016
NM_025265.4(TSEN2):c.472G>A (p.Val158Ile)	rs763286358	0.00004
NM_025265.4(TSEN2):c.241T>G (p.Ser81Ala)	rs774798241	0.00003
NM_025265.4(TSEN2):c.1369C>T (p.Arg457Ter)	rs139032110	0.00001
NM_025265.4(TSEN2):c.431A>G (p.Asn144Ser)	rs778603443	0.00001
NM_025265.4(TSEN2):c.784G>A (p.Glu262Lys)	rs770220924	0.00001
NM_025265.4(TSEN2):c.1063G>T (p.Val355Leu)	rs368652521
NM_025265.4(TSEN2):c.1136+4C>T
NM_025265.4(TSEN2):c.1311_1317delinsTTTA (p.Glu438_Cys439delinsLeu)
NM_025265.4(TSEN2):c.1338+1G>A
NM_025265.4(TSEN2):c.331G>A (p.Ala111Thr)	rs545512354
NM_025265.4(TSEN2):c.727A>G (p.Ile243Val)	rs2125050014
NM_025265.4(TSEN2):c.871T>C (p.Tyr291His)	rs2125059760

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.