ClinVar Miner

List of variants in gene TOE1 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025077.4(TOE1):c.1160A>G (p.Asp387Gly) rs144714540 0.00021
NM_025077.4(TOE1):c.550C>T (p.Arg184Cys) rs533647558 0.00011
NM_025077.4(TOE1):c.776G>A (p.Arg259Gln) rs144829269 0.00006
NM_025077.4(TOE1):c.880C>A (p.Pro294Thr) rs770784428 0.00006
NM_025077.4(TOE1):c.757C>T (p.Arg253Trp) rs368182654 0.00005
NM_025077.4(TOE1):c.638C>A (p.Thr213Asn) rs575022056 0.00004
NM_025077.4(TOE1):c.1104G>C (p.Lys368Asn) rs897395395 0.00003
NM_025077.4(TOE1):c.1481G>A (p.Arg494His) rs745910227 0.00003
NM_025077.4(TOE1):c.1159G>A (p.Asp387Asn) rs140119746 0.00002
NM_025077.4(TOE1):c.533T>G (p.Leu178Arg) rs774216136 0.00002
NM_025077.4(TOE1):c.1016G>A (p.Arg339Gln) rs776880897 0.00001
NM_025077.4(TOE1):c.1358A>T (p.Tyr453Phe) rs1300042760 0.00001
NM_025077.4(TOE1):c.1469G>A (p.Ser490Asn) rs1647092857 0.00001
NM_025077.4(TOE1):c.204T>G (p.Ser68Arg) rs1646952687 0.00001
NM_025077.4(TOE1):c.554G>A (p.Arg185Gln) rs535191956 0.00001
NM_025077.4(TOE1):c.745C>T (p.Arg249Trp) rs771979228 0.00001
NM_025077.4(TOE1):c.866C>T (p.Pro289Leu) rs1441910329 0.00001
NM_025077.4(TOE1):c.1010G>A (p.Arg337Gln)
NM_025077.4(TOE1):c.1034G>A (p.Arg345Gln)
NM_025077.4(TOE1):c.1058C>T (p.Pro353Leu)
NM_025077.4(TOE1):c.1063A>T (p.Thr355Ser)
NM_025077.4(TOE1):c.1097C>T (p.Pro366Leu)
NM_025077.4(TOE1):c.1157C>A (p.Ala386Asp)
NM_025077.4(TOE1):c.115G>T (p.Val39Leu)
NM_025077.4(TOE1):c.1189C>A (p.Gln397Lys)
NM_025077.4(TOE1):c.1213_1215dup (p.Met405_Gly406insMet)
NM_025077.4(TOE1):c.1240del (p.Glu413_Ile414insTer) rs2149260896
NM_025077.4(TOE1):c.1264G>A (p.Val422Met)
NM_025077.4(TOE1):c.1315C>T (p.Arg439Trp)
NM_025077.4(TOE1):c.132C>A (p.Phe44Leu)
NM_025077.4(TOE1):c.1379C>A (p.Pro460Gln) rs149059377
NM_025077.4(TOE1):c.1393T>C (p.Ser465Pro)
NM_025077.4(TOE1):c.1405C>T (p.Leu469Phe)
NM_025077.4(TOE1):c.1439G>A (p.Gly480Asp) rs1442140372
NM_025077.4(TOE1):c.1476C>G (p.Phe492Leu)
NM_025077.4(TOE1):c.234C>A (p.Asn78Lys)
NM_025077.4(TOE1):c.242T>C (p.Ile81Thr)
NM_025077.4(TOE1):c.325C>A (p.Pro109Thr) rs1234401145
NM_025077.4(TOE1):c.337G>A (p.Glu113Lys)
NM_025077.4(TOE1):c.344C>T (p.Ser115Phe)
NM_025077.4(TOE1):c.371C>T (p.Thr124Ile)
NM_025077.4(TOE1):c.382A>G (p.Met128Val)
NM_025077.4(TOE1):c.416A>T (p.Gln139Leu)
NM_025077.4(TOE1):c.433G>A (p.Gly145Ser)
NM_025077.4(TOE1):c.453G>T (p.Gln151His)
NM_025077.4(TOE1):c.480G>C (p.Lys160Asn)
NM_025077.4(TOE1):c.494G>A (p.Gly165Asp)
NM_025077.4(TOE1):c.509G>T (p.Ser170Ile)
NM_025077.4(TOE1):c.553C>T (p.Arg185Trp)
NM_025077.4(TOE1):c.577C>T (p.Leu193Phe)
NM_025077.4(TOE1):c.581T>C (p.Ile194Thr)
NM_025077.4(TOE1):c.655T>C (p.Cys219Arg) rs1647056328
NM_025077.4(TOE1):c.718G>A (p.Val240Met)
NM_025077.4(TOE1):c.73A>T (p.Thr25Ser)
NM_025077.4(TOE1):c.746G>A (p.Arg249Gln)
NM_025077.4(TOE1):c.77C>G (p.Ser26Cys) rs1368830139
NM_025077.4(TOE1):c.787A>G (p.Ser263Gly)
NM_025077.4(TOE1):c.824C>A (p.Ser275Tyr)
NM_025077.4(TOE1):c.826A>G (p.Ser276Gly)
NM_025077.4(TOE1):c.850C>T (p.Arg284Cys)
NM_025077.4(TOE1):c.851G>A (p.Arg284His)
NM_025077.4(TOE1):c.868G>A (p.Ala290Thr)
NM_025077.4(TOE1):c.878G>A (p.Arg293His)
NM_025077.4(TOE1):c.911C>T (p.Ser304Leu) rs562110457
NM_025077.4(TOE1):c.912G>A (p.Ser304=)
NM_025077.4(TOE1):c.940C>G (p.Gln314Glu) rs555185290
NM_025077.4(TOE1):c.940_941del (p.Gln314fs) rs780563835

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.