ClinVar Miner

List of variants in gene TTN reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.29042-2A>C rs6716782 0.00060
NM_001267550.2(TTN):c.100400T>G (p.Val33467Gly) rs200166942 0.00045
NM_001267550.2(TTN):c.66172C>T (p.Arg22058Cys) rs199643269 0.00044
NM_001267550.2(TTN):c.21548G>A (p.Cys7183Tyr) rs189951108 0.00042
NM_001267550.2(TTN):c.1297G>A (p.Val433Ile) rs146000949 0.00031
NM_001267550.2(TTN):c.835C>T (p.Arg279Trp) rs138060032 0.00029
NM_001267550.2(TTN):c.84923A>C (p.Gln28308Pro) rs201674674 0.00025
NM_001267550.2(TTN):c.55306G>A (p.Glu18436Lys) rs201510986 0.00021
NM_001267550.2(TTN):c.26935A>C (p.Asn8979His) rs376982715 0.00018
NM_001267550.2(TTN):c.58397G>C (p.Gly19466Ala) rs201922910 0.00018
NM_001267550.2(TTN):c.106955G>A (p.Arg35652Gln) rs200497615 0.00016
NM_001267550.2(TTN):c.45979C>T (p.Arg15327Cys) rs367774903 0.00016
NM_001267550.2(TTN):c.25877A>G (p.Asn8626Ser) rs200355367 0.00015
NM_001267550.2(TTN):c.37873G>A (p.Val12625Met) rs1336768417 0.00015
NM_001267550.2(TTN):c.47936C>T (p.Pro15979Leu) rs184815126 0.00014
NM_001267550.2(TTN):c.84977G>A (p.Arg28326Gln) rs200843338 0.00014
NM_001267550.2(TTN):c.103912C>T (p.Arg34638Cys) rs374444254 0.00013
NM_001267550.2(TTN):c.17818T>C (p.Cys5940Arg) rs374882815 0.00012
NM_001267550.2(TTN):c.36737A>T (p.Glu12246Val) rs786205395 0.00012
NM_001267550.2(TTN):c.80160T>G (p.Ile26720Met) rs376363284 0.00012
NM_001267550.2(TTN):c.22091G>A (p.Arg7364Gln) rs200128066 0.00011
NM_001267550.2(TTN):c.88123C>T (p.Arg29375Cys) rs368439674 0.00011
NM_001267550.2(TTN):c.75914C>T (p.Pro25305Leu) rs142453163 0.00010
NM_001267550.2(TTN):c.44588C>T (p.Thr14863Met) rs759406486 0.00007
NM_001267550.2(TTN):c.56947G>A (p.Ala18983Thr) rs377000174 0.00007
NM_001267550.2(TTN):c.72824A>T (p.Lys24275Ile) rs199860952 0.00007
NM_001267550.2(TTN):c.49937G>A (p.Arg16646Gln) rs746384579 0.00006
NM_001267550.2(TTN):c.60343G>A (p.Asp20115Asn) rs369893671 0.00006
NM_001267550.2(TTN):c.6420T>A (p.Asp2140Glu) rs777009984 0.00006
NM_001267550.2(TTN):c.65389T>G (p.Cys21797Gly) rs375830234 0.00006
NM_001267550.2(TTN):c.13979C>T (p.Thr4660Met) rs754231728 0.00005
NM_001267550.2(TTN):c.56351G>A (p.Arg18784His) rs771284532 0.00005
NM_001267550.2(TTN):c.63464G>A (p.Arg21155His) rs373169150 0.00005
NM_001267550.2(TTN):c.80168G>A (p.Arg26723His) rs371615296 0.00005
NM_001267550.2(TTN):c.98866A>G (p.Met32956Val) rs727503538 0.00005
NM_001267550.2(TTN):c.102275G>A (p.Arg34092His) rs757918924 0.00004
NM_001267550.2(TTN):c.30826T>G (p.Ser10276Ala) rs778063825 0.00004
NM_001267550.2(TTN):c.42847C>T (p.Arg14283Cys) rs199684560 0.00004
NM_001267550.2(TTN):c.5264A>G (p.Asn1755Ser) rs201904897 0.00004
NM_001267550.2(TTN):c.58470T>A (p.Asp19490Glu) rs374118468 0.00004
NM_001267550.2(TTN):c.93179G>A (p.Arg31060His) rs776018262 0.00004
NM_001267550.2(TTN):c.26944G>A (p.Ala8982Thr) rs1384345252 0.00003
NM_001267550.2(TTN):c.28137A>G (p.Ile9379Met) rs1060500516 0.00003
NM_001267550.2(TTN):c.28204C>T (p.Arg9402Cys) rs369553799 0.00003
NM_001267550.2(TTN):c.50597G>A (p.Arg16866Lys) rs774137928 0.00003
NM_001267550.2(TTN):c.617C>A (p.Thr206Lys) rs768427369 0.00003
NM_001267550.2(TTN):c.72271G>C (p.Asp24091His) rs878924658 0.00003
NM_001267550.2(TTN):c.87815A>G (p.Tyr29272Cys) rs886039083 0.00003
NM_001267550.2(TTN):c.101282G>A (p.Arg33761Gln) rs774790424 0.00002
NM_001267550.2(TTN):c.14873A>G (p.Tyr4958Cys) rs530572005 0.00002
NM_001267550.2(TTN):c.16576A>C (p.Asn5526His) rs752558197 0.00002
NM_001267550.2(TTN):c.21970T>G (p.Tyr7324Asp) rs765632650 0.00002
NM_001267550.2(TTN):c.36142G>C (p.Val12048Leu) rs768872042 0.00002
NM_001267550.2(TTN):c.44222C>T (p.Thr14741Met) rs778576436 0.00002
NM_001267550.2(TTN):c.58351C>T (p.Arg19451Cys) rs763871350 0.00002
NM_001267550.2(TTN):c.60314T>G (p.Val20105Gly) rs727504490 0.00002
NM_001267550.2(TTN):c.69554G>A (p.Arg23185Gln) rs201448988 0.00002
NM_001267550.2(TTN):c.74378C>T (p.Ser24793Leu) rs766741890 0.00002
NM_001267550.2(TTN):c.74413G>A (p.Val24805Ile) rs371306826 0.00002
NM_001267550.2(TTN):c.74533A>C (p.Ile24845Leu) rs1214451388 0.00002
NM_001267550.2(TTN):c.80717G>A (p.Arg26906Gln) rs536183519 0.00002
NM_001267550.2(TTN):c.85846C>T (p.Arg28616Trp) rs754025981 0.00002
NM_001267550.2(TTN):c.87041G>A (p.Arg29014Gln) rs772536290 0.00002
NM_001267550.2(TTN):c.101728G>A (p.Glu33910Lys) rs943777958 0.00001
NM_001267550.2(TTN):c.103730A>G (p.Gln34577Arg) rs727505009 0.00001
NM_001267550.2(TTN):c.105049A>G (p.Thr35017Ala) rs368779151 0.00001
NM_001267550.2(TTN):c.105449G>A (p.Cys35150Tyr) rs554953169 0.00001
NM_001267550.2(TTN):c.107593G>A (p.Glu35865Lys) rs372841288 0.00001
NM_001267550.2(TTN):c.107723T>C (p.Ile35908Thr) rs769141222 0.00001
NM_001267550.2(TTN):c.1292C>T (p.Ala431Val) rs1417215136 0.00001
NM_001267550.2(TTN):c.22495A>G (p.Thr7499Ala) rs2078525840 0.00001
NM_001267550.2(TTN):c.26116G>A (p.Asp8706Asn) rs377074955 0.00001
NM_001267550.2(TTN):c.29183A>G (p.Asn9728Ser) rs374981132 0.00001
NM_001267550.2(TTN):c.44249A>G (p.Asn14750Ser) rs767633080 0.00001
NM_001267550.2(TTN):c.44870A>G (p.Glu14957Gly) rs796961766 0.00001
NM_001267550.2(TTN):c.46702C>T (p.Pro15568Ser) rs561728671 0.00001
NM_001267550.2(TTN):c.48022C>T (p.Arg16008Trp) rs374233884 0.00001
NM_001267550.2(TTN):c.55302G>A (p.Gln18434=) rs567251026 0.00001
NM_001267550.2(TTN):c.63269A>G (p.Tyr21090Cys) rs377480514 0.00001
NM_001267550.2(TTN):c.7758A>G (p.Ile2586Met) rs556000493 0.00001
NM_001267550.2(TTN):c.78259G>T (p.Asp26087Tyr) rs1169880412 0.00001
NM_001267550.2(TTN):c.80414A>C (p.Glu26805Ala) rs370095455 0.00001
NM_001267550.2(TTN):c.86614G>A (p.Asp28872Asn) rs1337280647 0.00001
NM_001267550.2(TTN):c.91385G>A (p.Arg30462Gln) rs794729529 0.00001
NM_001267550.2(TTN):c.94880T>C (p.Ile31627Thr) rs751714990 0.00001
NM_001267550.2(TTN):c.95562G>C (p.Trp31854Cys) rs752756889 0.00001
NM_001267550.2(TTN):c.97417C>T (p.Arg32473Cys) rs371924787 0.00001
NM_001267550.2(TTN):c.11605G>C (p.Val3869Leu) rs747929496
NM_001267550.2(TTN):c.13803C>G (p.Ile4601Met) rs2082097990
NM_001267550.2(TTN):c.1694C>A (p.Ser565Tyr) rs762175397
NM_001267550.2(TTN):c.177C>A (p.Ser59Arg) rs191057824
NM_001267550.2(TTN):c.25922-6T>G rs796983452
NM_001267550.2(TTN):c.26949A>T (p.Leu8983Phe) rs878969676
NM_001267550.2(TTN):c.28354G>C (p.Ala9452Pro) rs527663092
NM_001267550.2(TTN):c.35186AAG[1] (p.Glu11730del) rs1348719464
NM_001267550.2(TTN):c.41492T>C (p.Ile13831Thr) rs2154230322
NM_001267550.2(TTN):c.50653A>G (p.Ile16885Val) rs1405647586
NM_001267550.2(TTN):c.51443C>G (p.Pro17148Arg) rs2154198776
NM_001267550.2(TTN):c.55393G>T (p.Ala18465Ser) rs899078606
NM_001267550.2(TTN):c.57387T>G (p.Asn19129Lys) rs375305621
NM_001267550.2(TTN):c.64266A>C (p.Lys21422Asn) rs758963173
NM_001267550.2(TTN):c.65975T>A (p.Ile21992Asn) rs2154178211
NM_001267550.2(TTN):c.72104T>G (p.Phe24035Cys) rs759861907
NM_001267550.2(TTN):c.73232C>A (p.Ala24411Asp) rs55991022
NM_001267550.2(TTN):c.82610G>A (p.Gly27537Asp) rs555055615
NM_001267550.2(TTN):c.90819G>T (p.Lys30273Asn) rs1307577297
NM_001267550.2(TTN):c.92128C>A (p.Pro30710Thr) rs2154148331
NM_001267550.2(TTN):c.94032_94040dup (p.Val31346_Glu31347insAspIleVal) rs1697753486
NM_001267550.2(TTN):c.97592T>A (p.Val32531Glu) rs1060500477
NM_001267550.2(TTN):c.99478G>A (p.Val33160Ile) rs794729553

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