ClinVar Miner

List of variants in gene TRIM2 reported as likely benign for Charcot-Marie-Tooth disease type 2

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP
NM_015271.5(TRIM2):c.1050C>T (p.Ala350=) rs1433209136
NM_015271.5(TRIM2):c.1074G>A (p.Thr358=) rs145538082
NM_015271.5(TRIM2):c.1143C>T (p.Asp381=) rs116472166
NM_015271.5(TRIM2):c.1161C>T (p.Thr387=) rs144994337
NM_015271.5(TRIM2):c.1179C>T (p.Thr393=) rs376619155
NM_015271.5(TRIM2):c.1206C>T (p.Ser402=) rs770558554
NM_015271.5(TRIM2):c.122G>A (p.Arg41His) rs146705057
NM_015271.5(TRIM2):c.1434G>T (p.Val478=) rs751706975
NM_015271.5(TRIM2):c.1518A>G (p.Lys506=) rs773419235
NM_015271.5(TRIM2):c.1615-7C>G rs201299149
NM_015271.5(TRIM2):c.1671G>T (p.Pro557=) rs150231451
NM_015271.5(TRIM2):c.1698G>A (p.Val566=) rs747022098
NM_015271.5(TRIM2):c.1740T>C (p.Asp580=) rs756285274
NM_015271.5(TRIM2):c.189C>T (p.Leu63=) rs558845725
NM_015271.5(TRIM2):c.2055G>A (p.Lys685=) rs138490175
NM_015271.5(TRIM2):c.2085G>A (p.Gln695=) rs141479735
NM_015271.5(TRIM2):c.2139C>T (p.Ala713=) rs773958934
NM_015271.5(TRIM2):c.2169T>C (p.Phe723=) rs148412849
NM_015271.5(TRIM2):c.444C>T (p.His148=) rs771241708
NM_015271.5(TRIM2):c.519C>T (p.His173=) rs114900176
NM_015271.5(TRIM2):c.605+10C>A rs891133657
NM_015271.5(TRIM2):c.605+9C>A rs532381432
NM_015271.5(TRIM2):c.786+10G>A rs1268924136
NM_015271.5(TRIM2):c.816C>T (p.Leu272=) rs149607572
NM_015271.5(TRIM2):c.879G>A (p.Thr293=) rs115191942
NM_015271.5(TRIM2):c.927C>T (p.Asn309=) rs142242737
NM_015271.5(TRIM2):c.969C>T (p.Asn323=) rs116365246

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.