ClinVar Miner

List of variants in gene combination INSRR, NTRK1 reported by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014215.3(INSRR):c.2289G>A (p.Gln763=) rs56127838 0.02106
NM_014215.3(INSRR):c.1113C>T (p.Ser371=) rs140072588 0.00550
NM_014215.3(INSRR):c.1281C>G (p.Ser427=) rs140808257 0.00521
NM_014215.3(INSRR):c.3663-5A>G rs373122172 0.00385
NM_014215.3(INSRR):c.1811-5C>T rs189068345 0.00166
NM_014215.3(INSRR):c.3513C>T (p.Thr1171=) rs55694053 0.00068
NM_014215.3(INSRR):c.835C>T (p.Arg279Cys) rs150841787 0.00019
NM_014215.3(INSRR):c.775C>T (p.Leu259=) rs148794008 0.00012
NM_014215.3(INSRR):c.259C>T (p.Arg87Cys) rs374390533 0.00009

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.