ClinVar Miner

List of variants in gene NTRK1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_001007792.1(NTRK1):c.1223G>A (p.Arg408Gln) rs56320207
NM_001007792.1(NTRK1):c.123-3367G>A rs1007211
NM_001007792.1(NTRK1):c.1698-4del rs1799770
NM_001007792.1(NTRK1):c.1702C>T (p.His568Tyr) rs6336
NM_001007792.1(NTRK1):c.1730G>T (p.Gly577Val) rs6339
NM_001007792.1(NTRK1):c.1752C>T (p.Gly584=) rs6338
NM_001007792.1(NTRK1):c.1800G>A (p.Ala600=) rs17838192
NM_001007792.1(NTRK1):c.2094G>A (p.Thr698=) rs55668752
NM_001007792.1(NTRK1):c.2231G>A (p.Arg744Gln) rs35669708

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.