ClinVar Miner

List of variants reported as likely pathogenic for Dilated cardiomyopathy 1G

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ClinVar version:
Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.61876C>T (p.Arg20626Ter) rs72646846 0.00006
NM_001267550.2(TTN):c.6555_6556insTGTAAGGAAACAGACA (p.Lys2186fs) rs587780494 0.00003
NM_001267550.2(TTN):c.56572C>T (p.Arg18858Ter) rs745376275 0.00002
NM_001256850.1(TTN):c.51809dup (p.Asp17270fs) rs397517626 0.00001
NM_001267550.2(TTN):c.100587G>A (p.Trp33529Ter) rs1064793560 0.00001
NM_001267550.2(TTN):c.101107C>T (p.Arg33703Ter) rs766265889 0.00001
NM_001267550.2(TTN):c.44272C>T (p.Arg14758Ter) rs140743001 0.00001
NM_001267550.2(TTN):c.55660C>T (p.Arg18554Ter) rs1483931960 0.00001
NM_001267550.2(TTN):c.88837A>T (p.Lys29613Ter) rs794729300 0.00001
NM_001267550.2(TTN):c.90697C>T (p.Arg30233Ter) rs1553539391 0.00001
NM_001267550.2(TTN):c.95195C>T (p.Pro31732Leu) rs753334568 0.00001
NM_001267550.2(TTN):c.100590C>G (p.Tyr33530Ter) rs1489832770
NM_001267550.2(TTN):c.10115-1G>C rs2088245783
NM_001267550.2(TTN):c.101247dup (p.Ile33750fs)
NM_001267550.2(TTN):c.102352C>T (p.Arg34118Ter) rs1212204584
NM_001267550.2(TTN):c.102749del (p.Thr34250fs) rs2154135490
NM_001267550.2(TTN):c.102953T>G (p.Leu34318Ter)
NM_001267550.2(TTN):c.103705A>T (p.Lys34569Ter) rs1553490574
NM_001267550.2(TTN):c.103710G>A (p.Trp34570Ter)
NM_001267550.2(TTN):c.105251C>G (p.Ser35084Ter)
NM_001267550.2(TTN):c.106928_106932del (p.Val35643fs)
NM_001267550.2(TTN):c.13115del (p.Val4372fs) rs2154317965
NM_001267550.2(TTN):c.13807del (p.Glu4603fs) rs1574066113
NM_001267550.2(TTN):c.13898_13899del (p.Lys4633fs) rs2154317474
NM_001267550.2(TTN):c.22870G>T (p.Glu7624Ter)
NM_001267550.2(TTN):c.28462+1G>T rs2076520917
NM_001267550.2(TTN):c.3283del (p.Glu1095fs)
NM_001267550.2(TTN):c.3664C>T (p.Gln1222Ter) rs1227198694
NM_001267550.2(TTN):c.38182A>T (p.Lys12728Ter)
NM_001267550.2(TTN):c.40558G>C (p.Val13520Leu) rs587780488
NM_001267550.2(TTN):c.40626dup (p.Pro13543fs) rs1553754743
NM_001267550.2(TTN):c.40663G>T (p.Glu13555Ter)
NM_001267550.2(TTN):c.40688_40689insT (p.Arg13565fs) rs2154238038
NM_001267550.2(TTN):c.44294dup (p.Leu14766fs)
NM_001267550.2(TTN):c.46344del (p.Ile15448_Ile15449insTer)
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs) rs756433029
NM_001267550.2(TTN):c.47576_47577delGA rs1060500489
NM_001267550.2(TTN):c.48305G>A (p.Trp16102Ter)
NM_001267550.2(TTN):c.48638+1del
NM_001267550.2(TTN):c.48963_48966del (p.Ser16321fs) rs1553703310
NM_001267550.2(TTN):c.50723del (p.Lys16908fs)
NM_001267550.2(TTN):c.50914_50918del (p.Leu16972fs) rs2056249919
NM_001267550.2(TTN):c.51234_51237dup (p.Leu17080fs) rs1553693444
NM_001267550.2(TTN):c.51444del (p.Asp17149fs) rs1362409861
NM_001267550.2(TTN):c.51804_51805insCCAGTGCTATG (p.Ala17269fs) rs2154198510
NM_001267550.2(TTN):c.51925C>T (p.Gln17309Ter)
NM_001267550.2(TTN):c.52576_52603del (p.Asn17525_Ala17526insTer) rs1064792915
NM_001267550.2(TTN):c.52694_52695del (p.His17565fs)
NM_001267550.2(TTN):c.52731_52732del (p.Arg17577fs) rs878854315
NM_001267550.2(TTN):c.53848dup (p.Leu17950fs) rs1553682760
NM_001267550.2(TTN):c.54652C>T (p.Arg18218Ter)
NM_001267550.2(TTN):c.55541_55542del (p.Tyr18514fs) rs1218695159
NM_001267550.2(TTN):c.55578G>A (p.Trp18526Ter)
NM_001267550.2(TTN):c.56679dup (p.Ser18894Ter) rs2052563186
NM_001267550.2(TTN):c.56830_56831del (p.Leu18944fs)
NM_001267550.2(TTN):c.57111_57111+9del rs1553661994
NM_001267550.2(TTN):c.57300_57303dup (p.Ile19102Ter) rs1553659902
NM_001267550.2(TTN):c.57998_57999del (p.Lys19333fs)
NM_001267550.2(TTN):c.59531_59570dup (p.Leu19857delinsPheSerTer) rs1064792914
NM_001267550.2(TTN):c.59535del (p.Asn19846fs) rs1559602980
NM_001267550.2(TTN):c.59647_59648del (p.Asp19883fs) rs878854322
NM_001267550.2(TTN):c.60359_60371del (p.Lys20120fs) rs2154184904
NM_001267550.2(TTN):c.60442dup (p.Glu20148fs)
NM_001267550.2(TTN):c.60457_60460del (p.Val20153fs)
NM_001267550.2(TTN):c.60621del (p.Asn20206_Tyr20207insTer) rs1060500442
NM_001267550.2(TTN):c.60865dup (p.Thr20289fs) rs1553643260
NM_001267550.2(TTN):c.61269del (p.Asp20424fs) rs1060500420
NM_001267550.2(TTN):c.62810_62813dup (p.Arg20939fs)
NM_001267550.2(TTN):c.63390_63393del (p.Phe21130fs)
NM_001267550.2(TTN):c.63801del (p.Pro21269fs) rs1553636843
NM_001267550.2(TTN):c.64011C>A (p.Tyr21337Ter) rs1553636324
NM_001267550.2(TTN):c.64245G>A (p.Trp21415Ter)
NM_001267550.2(TTN):c.64688del (p.Pro21563fs) rs774395395
NM_001267550.2(TTN):c.64688dup (p.Gln21564fs) rs774395395
NM_001267550.2(TTN):c.64752_64756del (p.Leu21585fs)
NM_001267550.2(TTN):c.6532C>T (p.Gln2178Ter) rs1193046655
NM_001267550.2(TTN):c.65531del (p.Pro21844fs) rs794729331
NM_001267550.2(TTN):c.66039del (p.Ser22014fs) rs1553628052
NM_001267550.2(TTN):c.66710del (p.Lys22237fs) rs1060500479
NM_001267550.2(TTN):c.66906_66907del (p.Asp22304fs)
NM_001267550.2(TTN):c.67166_67167del (p.Tyr22389fs) rs1476017129
NM_001267550.2(TTN):c.67613del (p.Thr22538fs)
NM_001267550.2(TTN):c.68087C>A (p.Ser22696Ter)
NM_001267550.2(TTN):c.68169_68171dup (p.Tyr22724Ter)
NM_001267550.2(TTN):c.68508dup (p.Val22837fs) rs1064793845
NM_001267550.2(TTN):c.69292_69299dup (p.Ala23101fs)
NM_001267550.2(TTN):c.70215dup (p.Asn23406Ter) rs1553614378
NM_001267550.2(TTN):c.71242del (p.Trp23748fs) rs1060500514
NM_001267550.2(TTN):c.71706del (p.Ile23902fs) rs2154171534
NM_001267550.2(TTN):c.72463del (p.Ile24155fs)
NM_001267550.2(TTN):c.72828_72831dup (p.Thr24278fs) rs751319893
NM_001267550.2(TTN):c.73200del (p.Ile24399_Tyr24400insTer)
NM_001267550.2(TTN):c.7433G>A (p.Trp2478Ter) rs1561254509
NM_001267550.2(TTN):c.74608del (p.Ala24870fs) rs878854332
NM_001267550.2(TTN):c.74767dup (p.Asp24923fs) rs1343078144
NM_001267550.2(TTN):c.75546C>A (p.Tyr25182Ter) rs1553603152
NM_001267550.2(TTN):c.75820_75823del (p.Glu25274fs)
NM_001267550.2(TTN):c.76115dup (p.Asn25372fs) rs774604740
NM_001267550.2(TTN):c.77013T>A (p.Tyr25671Ter)
NM_001267550.2(TTN):c.77147_77150del (p.Val25715_Ser25716insTer) rs1466647934
NM_001267550.2(TTN):c.77604T>G (p.Tyr25868Ter) rs752137856
NM_001267550.2(TTN):c.78110G>A (p.Trp26037Ter)
NM_001267550.2(TTN):c.78369_78376dup (p.Glu26126delinsAlaLeuTer)
NM_001267550.2(TTN):c.8017A>T (p.Lys2673Ter)
NM_001267550.2(TTN):c.80504del (p.Val26835fs)
NM_001267550.2(TTN):c.80762_80765del (p.Lys26921fs) rs2154164725
NM_001267550.2(TTN):c.81100_81103dup (p.Thr27035fs) rs1060500593
NM_001267550.2(TTN):c.82594dup (p.Thr27532fs) rs1064795407
NM_001267550.2(TTN):c.83048del (p.Lys27683fs) rs1060500572
NM_001267550.2(TTN):c.84311_84312del (p.Ile28104fs) rs1553565316
NM_001267550.2(TTN):c.84504dup (p.Ser28169fs)
NM_001267550.2(TTN):c.84969T>A (p.Tyr28323Ter)
NM_001267550.2(TTN):c.85589_85592del (p.Lys28530fs) rs1553562793
NM_001267550.2(TTN):c.86140G>T (p.Gly28714Ter)
NM_001267550.2(TTN):c.86822-2A>G rs773710035
NM_001267550.2(TTN):c.87077del (p.Pro29026fs)
NM_001267550.2(TTN):c.87315dup (p.Glu29106fs) rs1702181550
NM_001267550.2(TTN):c.87459_87460dup (p.Ser29154fs) rs2154155996
NM_001267550.2(TTN):c.87888del (p.Phe29297fs) rs1060500399
NM_001267550.2(TTN):c.88067G>A (p.Trp29356Ter) rs878854428
NM_001267550.2(TTN):c.89449G>T (p.Gly29817Ter)
NM_001267550.2(TTN):c.89900_89903del (p.Asn29967fs) rs869312081
NM_001267550.2(TTN):c.90495G>A (p.Trp30165Ter)
NM_001267550.2(TTN):c.9112T>C (p.Tyr3038His) rs886037909
NM_001267550.2(TTN):c.91257del (p.Val30420fs)
NM_001267550.2(TTN):c.91564+2T>C rs1699208458
NM_001267550.2(TTN):c.92173dup (p.Ile30725fs)
NM_001267550.2(TTN):c.92284_92288dup (p.Ser30763fs) rs756367933
NM_001267550.2(TTN):c.93396_93400del (p.Ala31133_Trp31134insTer) rs886044536
NM_001267550.2(TTN):c.94182_94183insAGCAGCT (p.Leu31395fs) rs1219954334
NM_001267550.2(TTN):c.94371del (p.Glu31458fs) rs1553524807
NM_001267550.2(TTN):c.95341C>T (p.Arg31781Ter) rs780414947
NM_001267550.2(TTN):c.95738del (p.Pro31913fs)
NM_001267550.2(TTN):c.95747_95753del (p.Pro31916fs)
NM_001267550.2(TTN):c.95772_95773del (p.His31924fs) rs1060500544
NM_001267550.2(TTN):c.96069dup (p.Val32024fs) rs878854432
NM_001267550.2(TTN):c.96464del (p.Val32155fs) rs2154143564
NM_001267550.2(TTN):c.96680_96684del (p.Leu32227fs)
NM_001267550.2(TTN):c.97114dup (p.Arg32372fs) rs1064793419
NM_001267550.2(TTN):c.97141_97145del (p.Leu32381fs)
NM_001267550.2(TTN):c.97451_97452del (p.Ser32484fs) rs878854433
NM_001267550.2(TTN):c.97472_97473del (p.Ile32491fs)
NM_001267550.2(TTN):c.98989+2T>C
NM_001267550.2(TTN):c.99034A>T (p.Lys33012Ter) rs771511344
NM_001267550.2(TTN):c.99588_99595del (p.Phe33196fs) rs1553504889
NM_001267550.2(TTN):c.99909del (p.Leu33303_Leu33304insTer)
NM_003319.4(TTN):c.53802_53817del (p.Ala17933_Tyr17934insTer) rs727503559
Single allele

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