ClinVar Miner

List of variants in gene TLR3 reported as likely benign for encephalomyelitis

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 125
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003265.3(TLR3):c.889C>G (p.Leu297Val) rs35311343 0.00165
NM_003265.3(TLR3):c.441+3A>G rs143625567 0.00091
NM_003265.3(TLR3):c.44T>G (p.Leu15Trp) rs149602022 0.00079
NM_003265.3(TLR3):c.2600G>A (p.Arg867Gln) rs199768900 0.00061
NM_003265.3(TLR3):c.66A>G (p.Ala22=) rs146166844 0.00060
NM_003265.3(TLR3):c.900A>G (p.Leu300=) rs147829071 0.00034
NM_003265.3(TLR3):c.2011C>T (p.Leu671=) rs144019953 0.00026
NM_003265.3(TLR3):c.165G>A (p.Val55=) rs139854420 0.00022
NM_003265.3(TLR3):c.2328A>G (p.Ser776=) rs370090850 0.00021
NM_003265.3(TLR3):c.2502T>C (p.His834=) rs151044075 0.00020
NM_003265.3(TLR3):c.2172C>T (p.His724=) rs374422592 0.00018
NM_003265.3(TLR3):c.34G>C (p.Gly12Arg) rs199539539 0.00016
NM_003265.3(TLR3):c.1716C>T (p.Asn572=) rs140712645 0.00013
NM_003265.3(TLR3):c.1295A>G (p.His432Arg) rs145303119 0.00011
NM_003265.3(TLR3):c.975G>A (p.Arg325=) rs574415152 0.00011
NM_003265.3(TLR3):c.1644C>T (p.His548=) rs147873871 0.00009
NM_003265.3(TLR3):c.1779A>G (p.Leu593=) rs200785357 0.00009
NM_003265.3(TLR3):c.2487-15C>T rs776864778 0.00007
NM_003265.3(TLR3):c.2487-17T>C rs529059095 0.00006
NM_003265.3(TLR3):c.1585C>T (p.Leu529Phe) rs201222071 0.00005
NM_003265.3(TLR3):c.387T>C (p.His129=) rs201726068 0.00005
NM_003265.3(TLR3):c.2487-18A>G rs5743319 0.00004
NM_003265.3(TLR3):c.2592C>T (p.Leu864=) rs200609786 0.00004
NM_003265.3(TLR3):c.450C>T (p.Ile150=) rs149945790 0.00004
NM_003265.3(TLR3):c.705C>G (p.Pro235=) rs776591694 0.00004
NM_003265.3(TLR3):c.174T>C (p.Leu58=) rs780632564 0.00003
NM_003265.3(TLR3):c.1890C>T (p.Phe630=) rs145921610 0.00003
NM_003265.3(TLR3):c.346G>A (p.Asp116Asn) rs140176180 0.00003
NM_003265.3(TLR3):c.957C>A (p.His319Gln) rs144596374 0.00003
NM_003265.3(TLR3):c.1605C>T (p.Leu535=) rs772360575 0.00002
NM_003265.3(TLR3):c.24C>T (p.Ile8=) rs192262541 0.00002
NM_003265.3(TLR3):c.1038T>A (p.Ile346=) rs757686834 0.00001
NM_003265.3(TLR3):c.1740G>A (p.Glu580=) rs953898407 0.00001
NM_003265.3(TLR3):c.1773C>T (p.Ile591=) rs757517639 0.00001
NM_003265.3(TLR3):c.177C>T (p.Thr59=) rs768368875 0.00001
NM_003265.3(TLR3):c.2523A>G (p.Glu841=) rs1232968295 0.00001
NM_003265.3(TLR3):c.333A>C (p.Leu111=) rs745694858 0.00001
NM_003265.3(TLR3):c.360C>T (p.Ala120=) rs375996512 0.00001
NM_003265.3(TLR3):c.369G>A (p.Thr123=) rs763487767 0.00001
NM_003265.3(TLR3):c.453A>G (p.Thr151=) rs1404118242 0.00001
NM_003265.3(TLR3):c.72C>T (p.Ser24=) rs762762392 0.00001
NM_003265.3(TLR3):c.735A>G (p.Leu245=) rs764010322 0.00001
NM_003265.3(TLR3):c.753G>A (p.Arg251=) rs1287228625 0.00001
NM_003265.3(TLR3):c.765G>A (p.Leu255=) rs948943852 0.00001
NM_003265.3(TLR3):c.798A>G (p.Thr266=) rs773691155 0.00001
NM_003265.3(TLR3):c.805T>C (p.Leu269=) rs748822809 0.00001
NM_003265.3(TLR3):c.873C>T (p.Asn291=) rs367695889 0.00001
NM_003265.3(TLR3):c.903A>G (p.Glu301=) rs555810983 0.00001
NM_003265.3(TLR3):c.915A>G (p.Leu305=) rs201480574 0.00001
NM_003265.3(TLR3):c.1035G>A (p.Lys345=)
NM_003265.3(TLR3):c.1044T>C (p.Asp348=)
NM_003265.3(TLR3):c.1119T>C (p.Asn373=)
NM_003265.3(TLR3):c.1149C>T (p.Tyr383=)
NM_003265.3(TLR3):c.1177T>C (p.Leu393=)
NM_003265.3(TLR3):c.1234C>T (p.Leu412Phe) rs3775291
NM_003265.3(TLR3):c.1383C>T (p.Ile461=) rs1377156808
NM_003265.3(TLR3):c.138C>T (p.Pro46=) rs267600111
NM_003265.3(TLR3):c.144T>C (p.Asp48=) rs2150066315
NM_003265.3(TLR3):c.1461C>T (p.Leu487=)
NM_003265.3(TLR3):c.1551C>T (p.Asn517=)
NM_003265.3(TLR3):c.1617T>C (p.His539=)
NM_003265.3(TLR3):c.165G>C (p.Val55=) rs139854420
NM_003265.3(TLR3):c.1681C>T (p.Leu561=)
NM_003265.3(TLR3):c.1698C>T (p.Ile566=)
NM_003265.3(TLR3):c.1713C>T (p.Ser571=) rs747344213
NM_003265.3(TLR3):c.1737T>C (p.Val579=)
NM_003265.3(TLR3):c.1830G>A (p.Val610=)
NM_003265.3(TLR3):c.1834C>T (p.Leu612=) rs781622881
NM_003265.3(TLR3):c.1872C>T (p.Ser624=)
NM_003265.3(TLR3):c.1902C>T (p.Phe634=)
NM_003265.3(TLR3):c.1911G>A (p.Leu637=)
NM_003265.3(TLR3):c.1923T>C (p.Asp641=)
NM_003265.3(TLR3):c.1929C>T (p.Arg643=)
NM_003265.3(TLR3):c.193A>C (p.Arg65=) rs1426754278
NM_003265.3(TLR3):c.1950G>A (p.Thr650=)
NM_003265.3(TLR3):c.1974T>G (p.Val658=) rs2150068080
NM_003265.3(TLR3):c.1977T>C (p.Asn659=)
NM_003265.3(TLR3):c.1986C>T (p.Asn662=) rs149490656
NM_003265.3(TLR3):c.1995T>C (p.His665=)
NM_003265.3(TLR3):c.2007T>C (p.Pro669=) rs1383149614
NM_003265.3(TLR3):c.2079A>C (p.Thr693=) rs1362142505
NM_003265.3(TLR3):c.2127T>C (p.Asn709=)
NM_003265.3(TLR3):c.2166C>T (p.Leu722=)
NM_003265.3(TLR3):c.2268T>C (p.Tyr756=)
NM_003265.3(TLR3):c.2292T>C (p.Tyr764=) rs2150068174
NM_003265.3(TLR3):c.2364G>T (p.Leu788=) rs764668957
NM_003265.3(TLR3):c.2382G>A (p.Glu794=) rs2150068194
NM_003265.3(TLR3):c.2385G>A (p.Ala795=) rs548804031
NM_003265.3(TLR3):c.2385G>T (p.Ala795=) rs548804031
NM_003265.3(TLR3):c.238T>C (p.Leu80=) rs2150066346
NM_003265.3(TLR3):c.2400A>G (p.Leu800=) rs781084129
NM_003265.3(TLR3):c.2409T>C (p.Ile803=)
NM_003265.3(TLR3):c.243T>C (p.Asp81=)
NM_003265.3(TLR3):c.2472C>T (p.Asp824=)
NM_003265.3(TLR3):c.2486+14G>A
NM_003265.3(TLR3):c.2487-4T>C rs2150068333
NM_003265.3(TLR3):c.2487-8T>C
NM_003265.3(TLR3):c.2517T>G (p.Ala839=)
NM_003265.3(TLR3):c.2655G>T (p.Arg885=) rs1441935850
NM_003265.3(TLR3):c.2661T>A (p.Gly887=)
NM_003265.3(TLR3):c.330G>A (p.Glu110=)
NM_003265.3(TLR3):c.333A>G (p.Leu111=) rs745694858
NM_003265.3(TLR3):c.39C>A (p.Gly13=) rs369957478
NM_003265.3(TLR3):c.39C>T (p.Gly13=) rs369957478
NM_003265.3(TLR3):c.411A>G (p.Lys137=)
NM_003265.3(TLR3):c.442-16T>C
NM_003265.3(TLR3):c.442-7C>G
NM_003265.3(TLR3):c.442-8C>T rs1579728263
NM_003265.3(TLR3):c.460C>T (p.Leu154=)
NM_003265.3(TLR3):c.528T>G (p.Leu176=)
NM_003265.3(TLR3):c.543T>C (p.Asn181=)
NM_003265.3(TLR3):c.555G>A (p.Ala185=)
NM_003265.3(TLR3):c.555G>C (p.Ala185=) rs545122782
NM_003265.3(TLR3):c.634-18T>C
NM_003265.3(TLR3):c.634-7C>T rs752550083
NM_003265.3(TLR3):c.717G>A (p.Glu239=) rs2150067659
NM_003265.3(TLR3):c.753G>C (p.Arg251=)
NM_003265.3(TLR3):c.789C>G (p.Thr263=)
NM_003265.3(TLR3):c.813A>G (p.Leu271=)
NM_003265.3(TLR3):c.894A>T (p.Pro298=)
NM_003265.3(TLR3):c.906T>C (p.Tyr302=)
NM_003265.3(TLR3):c.90T>C (p.Val30=)
NM_003265.3(TLR3):c.957C>T (p.His319=) rs144596374
NM_003265.3(TLR3):c.972G>A (p.Val324=) rs376729684
NM_003265.3(TLR3):c.972G>T (p.Val324=) rs376729684

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.