ClinVar Miner

List of variants in gene MTMR14 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001077525.3(MTMR14):c.727A>G (p.Thr243Ala) rs201904466 0.00040
NM_001077525.3(MTMR14):c.1144C>T (p.Arg382Trp) rs757251437 0.00006
NM_001077525.3(MTMR14):c.1893C>T (p.Gly631=) rs770888067 0.00001
NM_001077525.3(MTMR14):c.1295-7_1295-5del rs771401637
NM_001077525.3(MTMR14):c.256C>T (p.Pro86Ser) rs1574920079
NM_001077525.3(MTMR14):c.482A>C (p.Tyr161Ser) rs200189498

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.