All variants in the TNNT2 gene

Information The variants shown are described using the NM_001001430.1 transcript reference sequence.

185 entries on 2 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. 14 c.690 - - novel; The mutation occurred within a not highly conserved location and was therefore considered a v - GenBank TNNT2_00078 - Substitution - Qi Ming
./. 08 c.? - - - - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 08 c.? - p.= new - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 09 c.? - p.= - - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 09 c.? - p.= - - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 08 c.? - p.Glu87Lys? - - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 09 c.? - p.Pro120Val associated with a benign or malignant prognosis - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 09 c.? - p.Arg102Leu associated with a benign or malignant prognosis - GenBank TNNT2_00005 - Substitution - Qi Ming
./. 03 c.?_(?+5)del - p.= - - GenBank TNNT2_00104 - Deletion - Qi Ming
./. 04 c.53-36_53-32del - p.= - - GenBank TNNT2_00059 49% Deletion - Qi Ming
./. 04 c.53-34_53-30dup - p.= a common polymorphism - GenBank TNNT2_00061 - Duplication - Qi Ming
./. 05 c.83C>T - p.Ala28Val - - GenBank TNNT2_00045 - Substitution - Qi Ming
./. 05 c.83C>T - p.Ala28Val The carrier is asymptomatic - GenBank TNNT2_00045 1% Substitution - Qi Ming
./. 06 c.134-50G>A - p.= polymorphism - GenBank TNNT2_00049 37% Substitution - Qi Ming
./. 06 c.134-50G>A - p.= polymorphism - GenBank TNNT2_00049 - Substitution - Qi Ming
./. 07 c.170-29C>G - p.= rare - GenBank TNNT2_00052 - Substitution - Qi Ming
./. 08 c.206C>T - p.Ser69Leu - - GenBank TNNT2_00016 - Substitution - Qi Ming
./. 08 c.207G>A - p.= appear frequently in the normal population - GenBank TNNT2_00026 - Substitution - Qi Ming
./. 08 c.207G>A - p.Ser69Ser - - GenBank TNNT2_00026 0.04 Substitution - Qi Ming
./. 08 c.207G>A - p.= polymorphism - GenBank TNNT2_00026 0.12 Substitution - Qi Ming
./. 08 c.207G>A - p.Ser69Ser Polymorphism - GenBank TNNT2_00026 - Substitution - Qi Ming
./. 08 c.207G>A - p.Ser69Ser - - GenBank TNNT2_00026 10% Substitution - Qi Ming
./. 08 c.207G>C - p.Ser69Ser - - GenBank TNNT2_00103 - Substitution - Qi Ming
./. 08 c.208T>C - p.Phe70Leu associated with a benign or malignant prognosis - GenBank TNNT2_00107 - Substitution - Qi Ming
./. 08 c.210C>A - p.Phe70Leu - - GenBank TNNT2_00031 - Substitution - Qi Ming
./. 08 c.230C>T - p.Pro77Leu - - GenBank TNNT2_00015 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn - - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn - - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn - - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn affects a residue that is conserved among all known sequences of cardiac troponin T; characterized b - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn cause a definite increase in Ca21 sensitivity of the myofibrillar ATPase activity - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.236T>A - p.Ile79Asn The lle79Asn missense in cardliac troponin T affects a residue that is consetved in all kno - GenBank TNNT2_00014 - Substitution - Qi Ming
./. 08 c.253G>C - p.Val85Leu - - GenBank TNNT2_00040 - Substitution - Qi Ming
./. 08 c.253G>C - p.Val85Leu - - GenBank TNNT2_00040 - Substitution - Qi Ming
./. 08 c.257A>T - p.Asp86Val - - GenBank TNNT2_00035 - Substitution - Qi Ming
./. 08 c.259T>C - p.Phe87Leu New; The mutation was associated with only mild hypertrophy but with a high risk of sudden death - GenBank TNNT2_00101 - Substitution - Qi Ming
./. 09 c.265-20C>T - - - - GenBank TNNT2_00004 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp A mutation, a C> T substitution in exon 9, was identified in a patient at position c.8772 in - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp novel - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp Longitudinal clinical evaluation of hypertrophic cardiomyopathy caused by cardiac troponin T gene - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp Mutation carriers, particularly males, suffered more SCD- or HF-related deaths than any other group - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp founder mutation;demonstrated significantly more abnormal blood pressure responses to exercise - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.274C>T - p.Arg92Trp - - GenBank TNNT2_00011 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln weakening folding and stability to a small extent - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln affects a residue that is conserved among all known sequences of cardiac troponin T; characterized b - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln has a Ca2+ - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln mutations in TNN2 cause a less severe hypertrophy, but a high risk of SCD. - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln the Arg92Gln mutation substitutes an uncharges residue at a position invariably occupied by - GenBank TNNT2_00071 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln - - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>A - p.Arg92Gln The mutation was confirmed by the loss, in the affected individuals, of a 105 bp fragment within e - GenBank TNNT2_00008 - Substitution - Qi Ming
./. 09 c.275G>T - p.Arg92Leu - - GenBank TNNT2_00012 - Substitution - Qi Ming
./. 09 c.275G>T - p.Arg92Leu - - GenBank TNNT2_00012 - Substitution - Qi Ming
./. 09 c.275G>T - p.Arg92Leu - - GenBank TNNT2_00012 - Substitution - Qi Ming
./. 09 c.280C>T - p.Arg94Cys novel; occur at a CpG site - GenBank TNNT2_00030 - Substitution - Qi Ming
./. 09 c.281G>A - p.Arg94His due to deamination of the symmetrical 5mC residue in the antisense strand - GenBank TNNT2_00028 - Substitution - Qi Ming
./. 09 c.281G>T - p.Arg94Leu - - GenBank TNNT2_00013 - Substitution - Qi Ming
./. 09 c.281G>T - p.Arg94Leu - - GenBank TNNT2_00013 - Substitution - Qi Ming
./. 09 c.286G>A - p.Glu96Lys - - GenBank TNNT2_00109 - Substitution - Qi Ming
./. 09 c.291G>A - p.Lys97Lys - - GenBank TNNT2_00102 - Substitution - Qi Ming
./. 09 c.311C>T - p.Ala104Val - - GenBank TNNT2_00017 - Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile The polymorphism identified was a C> T substitution at position c.8816, which changes the - GenBank TNNT2_00003 - Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile occurs within a CpG site - GenBank TNNT2_00029 - Substitution - Qi Ming
./. 09 c.318C>T - p.= a common polymorphism - GenBank TNNT2_00029 - Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile - - GenBank TNNT2_00029 0.30 Substitution - Qi Ming
./. 09 c.318C>T - p.= polymorphism - GenBank TNNT2_00029 0.27 Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile Polymorphism - GenBank TNNT2_00029 - Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile - - GenBank TNNT2_00029 50% Substitution - Qi Ming
./. 09 c.318C>T - p.Ile106Ile - - GenBank TNNT2_00029 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile promoting folding and thermal stability assessed by circular dichroism - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile The mutaiton causes hypertrophic cardiomyopathy with variable cardiac morphologies and a favorable p - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile - - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile - - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile affects a residue that is conserved among all known sequences of cardiac troponin T; characterized b - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile remarkably potentiated the maximum level of ATPase activity - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile - - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile in a genomic hotspot; occurs in a conserved region of TnT that interacts with actin and tropomyosin - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>A - p.Phe110Ile - - GenBank TNNT2_00007 - Substitution - Qi Ming
./. 09 c.328T>C - p.Phe110Leu new; located in a highly conserved region coding for the tropomyosin binding site. - GenBank TNNT2_00057 - Substitution - Qi Ming
./. 09 c.330T>C - p.= appear frequently in the normal population - GenBank TNNT2_00023 - Substitution - Qi Ming
./. 09 c.361G>A - p.Val121Ile due to methylation in codon 120 - GenBank TNNT2_00027 - Substitution - Qi Ming
./. 10 c.382-97del - p.= Polymorphism - GenBank TNNT2_00056 - Deletion - Qi Ming
./. 10 c.388C>T - p.Arg130Cys - - GenBank TNNT2_00058 - Substitution - Qi Ming
./. 10 c.388C>T - p.Arg130Cys It expressed malignant phenotype - GenBank TNNT2_00058 2% Substitution - Qi Ming
./. 10 c.391C>T - p.Arg131Trp De novo mutation - GenBank TNNT2_00064 - Substitution - Qi Ming
./. 10 c.400C>G - P.Arg134Gly - - GenBank TNNT2_00072 - Substitution - Qi Ming
./. 10 c.400C>G - p.Arg134Gly novel - GenBank TNNT2_00072 - Substitution - Qi Ming
./. 10 c.406G>A - p.Glu136Lys new; occurred in functionally important and conserved regions of the genes - GenBank TNNT2_00069 - Substitution - Qi Ming
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