ClinVar Miner

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

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001256850.1(TTN):c.51809dup (p.Asp17270fs) rs397517626 0.00001
NM_001267550.2(TTN):c.47576_47577delGA rs1060500489
NM_001267550.2(TTN):c.51234_51237dup (p.Leu17080fs) rs1553693444
NM_001267550.2(TTN):c.52576_52603del (p.Asn17525_Ala17526insTer) rs1064792915
NM_001267550.2(TTN):c.52731_52732del (p.Arg17577fs) rs878854315
NM_001267550.2(TTN):c.53848dup (p.Leu17950fs) rs1553682760
NM_001267550.2(TTN):c.57111_57111+9del rs1553661994
NM_001267550.2(TTN):c.59531_59570dup (p.Leu19857delinsPheSerTer) rs1064792914
NM_001267550.2(TTN):c.59647_59648del (p.Asp19883fs) rs878854322
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.63801del (p.Pro21269fs) rs1553636843
NM_001267550.2(TTN):c.64688del (p.Pro21563fs) rs774395395
NM_001267550.2(TTN):c.64688dup (p.Gln21564fs) rs774395395
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.67166_67167del (p.Tyr22389fs) rs1476017129
NM_001267550.2(TTN):c.68508dup (p.Val22837fs) rs1064793845
NM_001267550.2(TTN):c.70215dup (p.Asn23406Ter) rs1553614378
NM_001267550.2(TTN):c.71242del (p.Trp23748fs) rs1060500514
NM_001267550.2(TTN):c.72828_72831dup (p.Thr24278fs) rs751319893
NM_001267550.2(TTN):c.74608del (p.Ala24870fs) rs878854332
NM_001267550.2(TTN):c.76115dup (p.Asn25372fs) rs774604740
NM_001267550.2(TTN):c.77147_77150del (p.Val25715_Ser25716insTer) rs1466647934
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.85589_85592del (p.Lys28530fs) rs1553562793
NM_001267550.2(TTN):c.87888del (p.Phe29297fs) rs1060500399
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.95772_95773del (p.His31924fs) rs1060500544
NM_001267550.2(TTN):c.96069dup (p.Val32024fs) rs878854432
NM_001267550.2(TTN):c.97114dup (p.Arg32372fs) rs1064793419
NM_001267550.2(TTN):c.97451_97452del (p.Ser32484fs) rs878854433
NM_001267550.2(TTN):c.99588_99595del (p.Phe33196fs) rs1553504889
NM_003319.4(TTN):c.53802_53817del (p.Ala17933_Tyr17934insTer) rs727503559

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