ClinVar Miner

List of variants in gene TMC1 reported as likely benign for Nonsyndromic Hearing Loss, Dominant

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP
NM_138691.2(TMC1):c.*106G>C rs79830675
NM_138691.2(TMC1):c.*156T>C rs545955592
NM_138691.2(TMC1):c.*183A>G rs71507808
NM_138691.2(TMC1):c.*28A>C rs151157872
NM_138691.2(TMC1):c.*93C>T rs184207177
NM_138691.2(TMC1):c.-329C>A rs7856724
NM_138691.2(TMC1):c.-540C>T rs112220638
NM_138691.2(TMC1):c.1457T>C (p.Met486Thr) rs17058153
NM_138691.2(TMC1):c.1713C>T (p.Phe571=) rs34532421
NM_138691.2(TMC1):c.1763+3A>G rs370898981
NM_138691.2(TMC1):c.238_240GAA[3] (p.Glu83del) rs376040866
NM_138691.2(TMC1):c.241G>A (p.Glu81Lys) rs1796993
NM_138691.2(TMC1):c.421C>T (p.Arg141Trp) rs11143384

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.