ClinVar Miner

List of variants in gene TTN reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP
NC_000002.12:g.178629314_178629316delTCT
NM_001256850.1(TTN):c.10188A>G (p.Glu3396=) rs183336802
NM_001256850.1(TTN):c.10360+5340C>T rs148105798
NM_001256850.1(TTN):c.11283C>G (p.Thr3761=) rs192857526
NM_001256850.1(TTN):c.1168G>A (p.Gly390Ser) rs794729412
NM_001256850.1(TTN):c.15630C>T (p.Val5210=) rs373179717
NM_001256850.1(TTN):c.25721A>G (p.Asn8574Ser) rs146057575
NM_001256850.1(TTN):c.32019_32036del18 (p.Glu10673_Tyr10678del) rs766756026
NM_001256850.1(TTN):c.33723C>T (p.Pro11241=) rs368781863
NM_001256850.1(TTN):c.63159C>T (p.Cys21053=) rs79406408
NM_001256850.1(TTN):c.64207C>T (p.Pro21403Ser) rs55980498
NM_001256850.1(TTN):c.71855T>A (p.Phe23952Tyr) rs547186080
NM_001256850.1(TTN):c.74421G>T (p.Val24807=) rs369875680
NM_001256850.1(TTN):c.74940G>A (p.Thr24980=) rs186402008
NM_001256850.1(TTN):c.76976G>A (p.Arg25659His) rs55850344
NM_001256850.1(TTN):c.77566G>A (p.Gly25856Arg) rs201158906
NM_001256850.1(TTN):c.78593G>A (p.Arg26198Gln) rs376820301
NM_001256850.1(TTN):c.835C>T (p.Arg279Trp) rs138060032
NM_001256850.1(TTN):c.92176C>T (p.Arg30726Cys) rs202064385
NM_001256850.1(TTN):c.94595G>A (p.Cys31532Tyr) rs761362832
NM_001256850.1(TTN):c.95068T>C (p.Cys31690Arg) rs56061641
NM_001256850.1(TTN):c.95903G>A (p.Arg31968Gln) rs771243505
NM_001267550.2(TTN):c.104978C>A (p.Thr34993Lys)
NM_001267550.2(TTN):c.10654G>C (p.Ala3552Pro) rs774004409
NM_001267550.2(TTN):c.10712A>G (p.Asp3571Gly) rs769513424
NM_001267550.2(TTN):c.107387A>C (p.Glu35796Ala) rs1553478042
NM_001267550.2(TTN):c.107956A>G (p.Ile35986Val) rs1064797273
NM_001267550.2(TTN):c.13262A>G (p.Asn4421Ser) rs72648922
NM_001267550.2(TTN):c.27223G>A (p.Glu9075Lys)
NM_001267550.2(TTN):c.28966G>A (p.Asp9656Asn) rs1064797277
NM_001267550.2(TTN):c.29127C>G (p.Val9709=) rs769063245
NM_001267550.2(TTN):c.29944G>A (p.Ala9982Thr) rs200745162
NM_001267550.2(TTN):c.30492G>T (p.Glu10164Asp) rs1064797276
NM_001267550.2(TTN):c.34408A>G (p.Lys11470Glu) rs113942943
NM_001267550.2(TTN):c.35350C>T (p.Arg11784Cys) rs778615023
NM_001267550.2(TTN):c.41330-7T>A rs373636988
NM_001267550.2(TTN):c.43185C>A (p.Ala14395=) rs1057519234
NM_001267550.2(TTN):c.51617C>A (p.Thr17206Asn) rs1305177155
NM_001267550.2(TTN):c.54053A>T (p.Lys18018Met) rs368425364
NM_001267550.2(TTN):c.54401A>G (p.Asn18134Ser) rs971483896
NM_001267550.2(TTN):c.57092G>A (p.Gly19031Glu) rs1064797275
NM_001267550.2(TTN):c.64814G>A (p.Gly21605Asp) rs1553632971
NM_001267550.2(TTN):c.656C>T (p.Thr219Ile)
NM_001267550.2(TTN):c.70815G>A (p.Val23605=) rs55847238
NM_001267550.2(TTN):c.74600_74602delCAA (p.Thr24867del) rs543318580
NM_001267550.2(TTN):c.82825G>C (p.Val27609Leu) rs767367789
NM_001267550.2(TTN):c.84640A>G (p.Met28214Val) rs72648221
NM_001267550.2(TTN):c.89710C>T (p.Arg29904Cys)
NM_001267550.2(TTN):c.90764_90766delGAG (p.Gly30255del) rs748912340
NM_001267550.2(TTN):c.92595A>C (p.Leu30865Phe) rs192086736
NM_001267550.2(TTN):c.93162G>C (p.Glu31054Asp) rs1553530758
NM_001267550.2(TTN):c.97568C>G (p.Pro32523Arg)
NM_001267550.2(TTN):c.98989+1G>C
NM_001267550.2(TTN):c.99781C>T (p.Arg33261Cys) rs1064797274
NM_003319.4(TTN):c.18785G>A (p.Arg6262His) rs374697274
NM_133378.4(TTN):c.11446G>C (p.Val3816Leu) rs72648929
NM_133378.4(TTN):c.17816G>A (p.Cys5939Tyr) rs189951108
NM_133378.4(TTN):c.28892C>T (p.Pro9631Leu) rs72650031
NM_133378.4(TTN):c.31484-595A>T rs200840285
NM_133378.4(TTN):c.33817G>A (p.Asp11273Asn) rs201257644
NM_133378.4(TTN):c.39544G>A (p.Val13182Ile) rs72677232
NM_133378.4(TTN):c.43010G>A (p.Arg14337His) rs191539637
NM_133378.4(TTN):c.44435A>T (p.Asp14812Val) rs373305248
NM_133378.4(TTN):c.45418A>G (p.Lys15140Glu) rs185913848
NM_133378.4(TTN):c.49738A>G (p.Met16580Val) rs188185141
NM_133378.4(TTN):c.66898A>G (p.Ile22300Val) rs72646898
NM_133378.4(TTN):c.84751G>A (p.Val28251Ile) rs368511235
NM_133378.4(TTN):c.90056G>A (p.Arg30019His) rs55704830
NM_133378.4(TTN):c.95708G>A (p.Arg31903Gln) rs149391616
NM_133378.4(TTN):c.99872T>C (p.Met33291Thr) rs72629793
NM_133379.4(TTN):c.*265+198852C>T rs373871146
NM_133379.4(TTN):c.*265+213933G>A rs55938627
NM_133379.4(TTN):c.1054G>A (p.Ala352Thr) rs113324330
NM_133379.4(TTN):c.10844G>A (p.Arg3615Gln) rs747054427
NM_133379.4(TTN):c.11877C>A (p.Asp3959Glu) rs1482705228
NM_133379.4(TTN):c.13619A>T (p.His4540Leu) rs111233204
NM_133379.4(TTN):c.13948C>T (p.Pro4650Ser) rs149748934
NM_133379.4(TTN):c.15032A>C (p.Asp5011Ala) rs560037336

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