ClinVar Miner

List of variants in gene TFG studied for Charcot-Marie-Tooth disease

Included ClinVar conditions (137):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP
NM_006070.6(TFG):c.1006C>T (p.Pro336Ser) rs371681149
NM_006070.6(TFG):c.1014T>G (p.Asn338Lys) rs1553704923
NM_006070.6(TFG):c.1030G>A (p.Ala344Thr) rs1576389587
NM_006070.6(TFG):c.1036C>T (p.Gln346Ter) rs1576389617
NM_006070.6(TFG):c.1048G>A (p.Ala350Thr) rs543542721
NM_006070.6(TFG):c.1060C>G (p.Pro354Ala) rs111356679
NM_006070.6(TFG):c.1070A>G (p.Tyr357Cys) rs1375662436
NM_006070.6(TFG):c.1087T>G (p.Phe363Val)
NM_006070.6(TFG):c.1090A>C (p.Thr364Pro) rs6772054
NM_006070.6(TFG):c.1094C>T (p.Ser365Leu) rs1288104441
NM_006070.6(TFG):c.1116C>T (p.Thr372=) rs1576389880
NM_006070.6(TFG):c.1123C>G (p.Pro375Ala) rs1234073129
NM_006070.6(TFG):c.1133C>T (p.Pro378Leu)
NM_006070.6(TFG):c.1145C>T (p.Ala382Val) rs138185005
NM_006070.6(TFG):c.1146G>A (p.Ala382=) rs761808737
NM_006070.6(TFG):c.1153C>T (p.Arg385Cys)
NM_006070.6(TFG):c.1154G>A (p.Arg385His)
NM_006070.6(TFG):c.1157C>T (p.Pro386Leu) rs766049461
NM_006070.6(TFG):c.1165G>C (p.Gly389Arg) rs1576390105
NM_006070.6(TFG):c.1172G>T (p.Gly391Val)
NM_006070.6(TFG):c.1199G>A (p.Arg400Gln) rs963151000
NM_006070.6(TFG):c.1199G>C (p.Arg400Pro)
NM_006070.6(TFG):c.185-10T>A rs79631225
NM_006070.6(TFG):c.185-9A>T rs778438842
NM_006070.6(TFG):c.196A>G (p.Ile66Val)
NM_006070.6(TFG):c.237G>T (p.Gln79His) rs1173009495
NM_006070.6(TFG):c.256C>G (p.Leu86Val)
NM_006070.6(TFG):c.258G>T (p.Leu86=) rs150620449
NM_006070.6(TFG):c.268G>A (p.Val90Ile)
NM_006070.6(TFG):c.286C>T (p.Pro96Ser)
NM_006070.6(TFG):c.290T>A (p.Leu97His) rs1576366321
NM_006070.6(TFG):c.302A>G (p.Gln101Arg) rs1576366326
NM_006070.6(TFG):c.309A>G (p.Lys103=) rs369508900
NM_006070.6(TFG):c.310T>C (p.Tyr104His) rs775608477
NM_006070.6(TFG):c.316C>T (p.Arg106Cys) rs587777175
NM_006070.6(TFG):c.391C>T (p.Pro131Ser) rs770053266
NM_006070.6(TFG):c.395C>A (p.Ser132Tyr)
NM_006070.6(TFG):c.409G>C (p.Glu137Gln)
NM_006070.6(TFG):c.415+7C>G rs149927288
NM_006070.6(TFG):c.416-9T>C rs115896544
NM_006070.6(TFG):c.457T>G (p.Ser153Ala) rs140466338
NM_006070.6(TFG):c.458C>T (p.Ser153Phe) rs775354552
NM_006070.6(TFG):c.464A>G (p.Lys155Arg)
NM_006070.6(TFG):c.467A>G (p.Gln156Arg)
NM_006070.6(TFG):c.482T>C (p.Met161Thr) rs766899074
NM_006070.6(TFG):c.483G>A (p.Met161Ile) rs750964585
NM_006070.6(TFG):c.484G>A (p.Ala162Thr)
NM_006070.6(TFG):c.544A>C (p.Met182Leu)
NM_006070.6(TFG):c.545T>C (p.Met182Thr) rs199724547
NM_006070.6(TFG):c.552G>A (p.Ala184=) rs35648279
NM_006070.6(TFG):c.567T>A (p.Asp189Glu)
NM_006070.6(TFG):c.57G>A (p.Glu19=) rs1576353054
NM_006070.6(TFG):c.594T>G (p.Ala198=) rs12562
NM_006070.6(TFG):c.608G>A (p.Arg203His)
NM_006070.6(TFG):c.621C>T (p.Pro207=) rs141786985
NM_006070.6(TFG):c.663C>A (p.Gly221=) rs140669729
NM_006070.6(TFG):c.663C>T (p.Gly221=) rs140669729
NM_006070.6(TFG):c.664G>A (p.Val222Ile)
NM_006070.6(TFG):c.672A>C (p.Pro224=) rs141412018
NM_006070.6(TFG):c.68G>A (p.Arg23Gln) rs774808090
NM_006070.6(TFG):c.716T>C (p.Ile239Thr) rs146004809
NM_006070.6(TFG):c.722-8G>T rs41272979
NM_006070.6(TFG):c.740A>G (p.Tyr247Cys) rs1559723912
NM_006070.6(TFG):c.741C>T (p.Tyr247=) rs1576379547
NM_006070.6(TFG):c.743A>G (p.Gln248Arg) rs1576379554
NM_006070.6(TFG):c.754G>A (p.Gly252Ser) rs561904697
NM_006070.6(TFG):c.771G>A (p.Gln257=) rs374006808
NM_006070.6(TFG):c.774G>A (p.Pro258=) rs1367793822
NM_006070.6(TFG):c.792G>T (p.Gln264His) rs1576379647
NM_006070.6(TFG):c.806G>T (p.Gly269Val) rs587777789
NM_006070.6(TFG):c.826T>C (p.Tyr276His) rs1559726842
NM_006070.6(TFG):c.852A>C (p.Gln284His) rs1559726965
NM_006070.6(TFG):c.854C>T (p.Pro285Leu) rs207482230
NM_006070.6(TFG):c.870A>G (p.Gly290=)
NM_006070.6(TFG):c.882A>C (p.Gln294His) rs751393611
NM_006070.6(TFG):c.898C>A (p.Pro300Thr)
NM_006070.6(TFG):c.898C>T (p.Pro300Ser) rs1210008384
NM_006070.6(TFG):c.908C>T (p.Ala303Val) rs1576389064
NM_006070.6(TFG):c.943C>T (p.Pro315Ser) rs1553704852
NM_006070.6(TFG):c.944C>T (p.Pro315Leu) rs753375115
NM_006070.6(TFG):c.945G>A (p.Pro315=) rs61736338
NM_006070.6(TFG):c.976G>T (p.Ala326Ser)
NM_006070.6(TFG):c.97T>C (p.Tyr33His)
NM_006070.6(TFG):c.980A>G (p.Gln327Arg) rs1431898500
NM_006070.6(TFG):c.988A>G (p.Thr330Ala) rs145835282
NM_006070.6(TFG):c.98A>G (p.Tyr33Cys) rs763523148
Single allele

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