ClinVar Miner

List of variants in gene OTOG reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
NM_001277269.1(OTOG):c.1389C>A (p.Phe463Leu) rs189947237
NM_001277269.1(OTOG):c.2819G>A (p.Cys940Tyr) rs1309976795
NM_001277269.1(OTOG):c.328+4A>C rs535970426
NM_001277269.1(OTOG):c.3371A>G (p.Asn1124Ser) rs571215839
NM_001277269.1(OTOG):c.3704C>T (p.Thr1235Ile) rs938096068
NM_001277269.1(OTOG):c.4009C>T (p.Arg1337Cys) rs557335789
NM_001277269.1(OTOG):c.5416C>T (p.Arg1806Cys) rs1246889104
NM_001277269.1(OTOG):c.6215G>A (p.Arg2072His) rs188527711
NM_001277269.1(OTOG):c.7081A>G (p.Ile2361Val) rs191722806
NM_001277269.1(OTOG):c.7570C>T (p.Arg2524Cys) rs533820347
NM_001277269.1(OTOG):c.7729+1G>A rs548496846
NM_001277269.1(OTOG):c.919G>A (p.Val307Met) rs186310325
NM_001277269.2(OTOG):c.[3719C>T] rs117005078
NM_001292063.2(OTOG):c.8018_8019delinsAT (p.Ala2673Asp) rs876657945

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.