ClinVar Miner

List of variants in gene TFG reported as benign for Charcot-Marie-Tooth disease

Included ClinVar conditions (127):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_006070.5(TFG):c.1090A>C (p.Thr364Pro) rs6772054
NM_006070.5(TFG):c.185-10T>C rs79631225
NM_006070.5(TFG):c.258G>T (p.Leu86=) rs150620449
NM_006070.5(TFG):c.415+7C>G rs149927288
NM_006070.5(TFG):c.416-9T>C rs115896544
NM_006070.5(TFG):c.552G>A (p.Ala184=) rs35648279
NM_006070.5(TFG):c.594T>G (p.Ala198=) rs12562
NM_006070.5(TFG):c.663C>A (p.Gly221=) rs140669729
NM_006070.5(TFG):c.722-8G>T rs41272979
NM_006070.5(TFG):c.945G>A (p.Pro315=) rs61736338

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.