List of variants in gene TSEN54 reported as pathogenic for central nervous system malformation

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_207346.3(TSEN54):c.919G>T (p.Ala307Ser)	rs113994152	0.00092
NM_207346.3(TSEN54):c.371G>T (p.Gly124Val)	rs774157225	0.00002
NM_207346.3(TSEN54):c.670_671del (p.Lys224fs)	rs762142684	0.00001
NM_207346.3(TSEN54):c.1027C>T (p.Gln343Ter)	rs113994154
NM_207346.3(TSEN54):c.1138G>T (p.Glu380Ter)	rs587784475
NM_207346.3(TSEN54):c.1172_1185del (p.Gln391fs)	rs886037629
NM_207346.3(TSEN54):c.1335del (p.Leu446fs)	rs587784476
NM_207346.3(TSEN54):c.1386_1387insTA (p.Lys463Ter)	rs797046054
NM_207346.3(TSEN54):c.1397dup (p.Gly467fs)	rs797046055
NM_207346.3(TSEN54):c.221+3G>T	rs2147005856
NM_207346.3(TSEN54):c.468+2T>C	rs886037740
NM_207346.3(TSEN54):c.575_576del (p.His192fs)	rs587784479
NM_207346.3(TSEN54):c.736C>T (p.Gln246Ter)	rs113994153
NM_207346.3(TSEN54):c.823del (p.Val275fs)	rs797046057
NM_207346.3(TSEN54):c.856_862dup (p.Val288fs)
NM_207346.3(TSEN54):c.869_875dup (p.Lys293fs)
NM_207346.3(TSEN54):c.940del (p.Leu314fs)	rs1012275384
NM_207346.3(TSEN54):c.953del (p.Pro318fs)
TSEN54:c.[277T>C;919G>T]

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.