List of variants in gene MTM1 reported as likely benign by GeneDx

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: 29

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000252.3(MTM1):c.1353+229A>G	rs138203673	0.02531
NM_000252.3(MTM1):c.1260+134C>T	rs144266984	0.01748
NM_000252.3(MTM1):c.343-100A>G	rs222389	0.01524
NM_000252.3(MTM1):c.1353+262C>T	rs111951773	0.01403
NM_000252.3(MTM1):c.1053+105A>C	rs140153689	0.01044
NM_000252.3(MTM1):c.528+1035G>A	rs140625961	0.01025
NM_000252.3(MTM1):c.-10-248C>T	rs111468862	0.00734
NM_000252.3(MTM1):c.343-158A>G	rs191242850	0.00706
NM_000252.3(MTM1):c.63+252C>T	rs189339138	0.00636
NM_000252.3(MTM1):c.*182C>T	rs222419	0.00587
NM_000252.3(MTM1):c.445-33C>T	rs143521383	0.00507
NM_000252.3(MTM1):c.64-198A>G	rs188412335	0.00482
NM_000252.3(MTM1):c.529-324G>A	rs782664286	0.00390
NM_000252.3(MTM1):c.529-76G>A	rs782310438	0.00367
NM_000252.3(MTM1):c.232-54A>T	rs143312552	0.00356
NM_000252.3(MTM1):c.867+13A>C	rs368954714	0.00051
NM_000252.3(MTM1):c.582C>T (p.Leu194=)	rs367912069	0.00029
NM_000252.3(MTM1):c.867+17A>G	rs371239013	0.00017
NM_000252.3(MTM1):c.231+30C>A	rs368915645	0.00010
NM_000252.3(MTM1):c.1454C>T (p.Ala485Val)	rs782137551	0.00001
NM_000252.3(MTM1):c.1468-10C>T	rs782174623	0.00001
NM_000252.3(MTM1):c.444+16C>G	rs1057523163	0.00001
NM_000252.3(MTM1):c.136+172=	rs222380
NM_000252.3(MTM1):c.343-192C>T	rs7884615
NM_000252.3(MTM1):c.405G>A (p.Glu135=)	rs1557413212
NM_000252.3(MTM1):c.528+6A>G	rs1057521934
NM_000252.3(MTM1):c.63+183dup	rs1184716210
NM_000252.3(MTM1):c.63+7del	rs782222093
NM_000252.3(MTM1):c.679-150C>G	rs113515087

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.