ClinVar Miner

List of variants in gene TTN reported as uncertain significance for Primary dilated cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
Download table as spreadsheet
HGVS dbSNP
NM_001256850.1(TTN):c.28091-2A>C rs6716782
NM_001256850.1(TTN):c.30812-1G>A rs202234172
NM_001256850.1(TTN):c.325C>T (p.Arg109Ter) rs150954246
NM_001256850.1(TTN):c.39358C>T (p.Pro13120Ser) rs192766485
NM_001256850.1(TTN):c.87361_87365dupAAAAG (p.Ser29122Argfs) rs756367933
NM_001267550.2(TTN):c.102630delA (p.Val34211Terfs) rs869312101
NM_001267550.2(TTN):c.103408G>T (p.Glu34470Ter) rs769023413
NM_001267550.2(TTN):c.104092C>T (p.Arg34698Ter) rs727504184
NM_001267550.2(TTN):c.10592C>G (p.Ser3531Ter) rs767420661
NM_001267550.2(TTN):c.106374+1delG rs763404256
NM_001267550.2(TTN):c.10799C>A (p.Ser3600Ter) rs374300381
NM_001267550.2(TTN):c.10852C>T (p.Gln3618Ter) rs779064556
NM_001267550.2(TTN):c.11113delA (p.Arg3705Aspfs) rs746386040
NM_001267550.2(TTN):c.1245+3A>G rs757221300
NM_001267550.2(TTN):c.15776-1G>T rs869312094
NM_001267550.2(TTN):c.21142C>T (p.Arg7048Ter) rs770579313
NM_001267550.2(TTN):c.23386C>T (p.Arg7796Ter) rs748111134
NM_001267550.2(TTN):c.2494G>T (p.Ala832Ser) rs376133574
NM_001267550.2(TTN):c.26893G>A (p.Glu8965Lys) rs200325324
NM_001267550.2(TTN):c.27328+5G>A rs397517521
NM_001267550.2(TTN):c.27607G>A (p.Glu9203Lys) rs769097909
NM_001267550.2(TTN):c.2841G>T (p.Ser947=) rs774074192
NM_001267550.2(TTN):c.30803-2A>G rs869312089
NM_001267550.2(TTN):c.31426+1G>C rs6749719
NM_001267550.2(TTN):c.31594G>T (p.Val10532Phe) rs763955552
NM_001267550.2(TTN):c.31762G>A (p.Val10588Ile) rs372371333
NM_001267550.2(TTN):c.32095+5G>A rs869312090
NM_001267550.2(TTN):c.32554+1G>C rs376018437
NM_001267550.2(TTN):c.33418+1G>A rs746588865
NM_001267550.2(TTN):c.34132del (p.Leu11378Tyrfs) rs869025551
NM_001267550.2(TTN):c.39044-9T>A rs184888200
NM_001267550.2(TTN):c.39895+1G>T rs749931280
NM_001267550.2(TTN):c.40558+1G>A rs368219776
NM_001267550.2(TTN):c.45391delA (p.Ile15131Tyrfs) rs869312091
NM_001267550.2(TTN):c.48460+5G>A rs374413644
NM_001267550.2(TTN):c.52128delT (p.Phe17376Leufs) rs869312095
NM_001267550.2(TTN):c.53881+5G>A rs753527304
NM_001267550.2(TTN):c.57544+4A>G rs869312053
NM_001267550.2(TTN):c.57847+5_57847+8delGTAA rs587782988
NM_001267550.2(TTN):c.6355G>T (p.Glu2119Ter) rs869312098
NM_001267550.2(TTN):c.67159delA (p.Ile22387Terfs) rs869312092
NM_001267550.2(TTN):c.7330+5G>C rs869025547
NM_001267550.2(TTN):c.75123T>A (p.Tyr25041Ter) rs753526510
NM_001267550.2(TTN):c.80635C>T (p.Gln26879Ter) rs79926414
NM_001267550.2(TTN):c.85008_85011delTAGT (p.Glu28338Hisfs) rs869312100
NM_001267550.2(TTN):c.87716delG (p.Gly29239Aspfs) rs869312028
NM_001267550.2(TTN):c.9164-2A>T rs777369921
NM_001267550.2(TTN):c.91715dup (p.Asn30572Lysfs) rs779129892
NM_001267550.2(TTN):c.96892C>T (p.Gln32298Ter) rs201108270
NM_001267550.2(TTN):c.97192+4A>G rs370069759
NM_001267550.2(TTN):c.9727C>T (p.Gln3243Ter) rs869312093
NM_001267550.2(TTN):c.98551C>T (p.Arg32851Ter) rs553821887
NM_003319.4(TTN):c.35311C>T (p.Arg11771Ter) rs757231565
NM_133378.4(TTN):c.10361-1G>A rs869312099
NM_133378.4(TTN):c.26542C>T (p.His8848Tyr) rs72650011
NM_133378.4(TTN):c.3100G>A (p.Val1034Met) rs142951505
NM_133378.4(TTN):c.32854G>C (p.Val10952Leu) rs587780488
NM_133378.4(TTN):c.61120G>A (p.Glu20374Lys) rs199506676
NM_133379.4(TTN):c.10443delA (p.Lys3481Asnfs) rs869312096
NM_133379.4(TTN):c.13022C>G (p.Ser4341Ter) rs763408700
NM_133379.4(TTN):c.13410dup (p.Gly4471Argfs) rs768458450
NM_133379.4(TTN):c.13660dup (p.Ile4554Asnfs) rs771985828
NM_133379.4(TTN):c.13705G>T (p.Glu4569Ter) rs372994805
NM_133379.4(TTN):c.13939delG (p.Glu4647Lysfs) rs781363456
NM_133379.4(TTN):c.14460_14470dup (p.Arg4824Thrfs) rs869312088
NM_133379.4(TTN):c.15305delC (p.Thr5102Ilefs) rs869312097
NM_133379.4(TTN):c.16516G>T (p.Glu5506Ter) rs148430495
NM_133379.4(TTN):c.16529delT (p.Val5510Glyfs) rs774991940
NM_133437.4(TTN):c.10670dup (p.Leu3558Thrfs) rs778172350

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.