All variants in the MYH7 gene

Information The variants shown are described using the NM_000257.2 transcript reference sequence.

559 entries on 6 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     
./. 00 c.1-2127A>T - - lymphocyte - GenBank MYH7_00015 - - - Qi Ming
./. 03 c.-8-25G>T - - blood - GenBank MYH7_00347 0.90 in patient - - Qi Ming
./. 03 c.-8-25G>T - - blood - GenBank MYH7_00184 - - - Qi Ming
./. int4 c.345+1G>A - - blood - GenBank MYH7_00351 - - - Qi Ming
./. 34 c.4660G>C - p.Glu1554Gln unknown - GenBank MYH7_00305 NA - - Qi Ming
./. 34 c.4660G>C - p.Glu1554Gln unknown - GenBank MYH7_00305 NA - - Qi Ming
./. 00 c.? - - blood - GenBank MYH7_00053 4/328 - - Qi Ming
./. 15 c.? - p.Glu497Asp blood - GenBank MYH7_00238 - the Glu497Asp mutation caused massive concentric hypertrophy (interventricular septum29 mm); after a syncopal episode, an automatic implanted cardioverter/ defibrillator was implanted in this patient - Qi Ming
./. 08 c.? - p.Arg237Cys peripheral blood - GenBank MYH7_00040 - - - Qi Ming
./. 03 c.1A>G - p.Met1Val unknown - GenBank MYH7_00343 NA - - Qi Ming
./. 03 c.8A>C - p.Asp3Ala unknown - GenBank MYH7_00342 NA - - Qi Ming
./. 03 c.11C>T - p.Ser4Leu blood - GenBank MYH7_00256 - - - Qi Ming
./. 03 c.29_31delGGG - p.Gly10del blood - GenBank MYH7_00187 - - - Qi Ming
./. 03 c.49C>T - p.Arg17Cys unknown - GenBank MYH7_00341 NA - - Qi Ming
./. 03 c.77C>T - p.Ala26Val blood - GenBank MYH7_00117 - - - Qi Ming
./. 03 c.77C>T - p.Ala26Val blood - GenBank MYH7_00117 - - - Qi Ming
./. 03 c.77C>T - p.Ala26Val unknown - GenBank MYH7_00117 NA - - Qi Ming
./. 03 c.115G>A - p.Val39Met blood - GenBank MYH7_00042 - - - Qi Ming
./. 03 c.160C>T - p.Arg54X Blood - GenBank MYH7_00271 - This is the first report of a nonsense mutation in the human cardiac ?-MHC gene. - Qi Ming
./. 03 c.189C>T - p.Thr63Thr lymphocyte - GenBank MYH7_00021 0.683 rs2069540 - Qi Ming
./. 03 c.189C>T - p.Thr63Thr blood - GenBank MYH7_00021 0.54 - - Qi Ming
./. 03 c.189C>T - p.Thr63Thr blood - GenBank MYH7_00021 - - - Qi Ming
./. 03 c.189C>T - p.Thr63Thr blood - GenBank MYH7_00021 - - - Qi Ming
./. 03 c.189C>T - p.Thr63Thr blood - GenBank MYH7_00021 - - - Qi Ming
./. 03 c.189C>T - p.Thr63Thr blood - GenBank MYH7_00021 - - - Qi Ming
./. 04 c.203C>A - p.Thr68Lys blood - GenBank MYH7_00043 - RLC binding domain and ATP binding domain. - Qi Ming
./. 04 c.321T>G - p.Asp107Glu unknown - GenBank MYH7_00340 NA - - Qi Ming
./. 04 c.343T>C - p.Tyr115His blood - GenBank MYH7_00148 - - - Qi Ming
./. 05 c.427C>G - p.Arg143Gly lymphocyte - GenBank MYH7_00014 - - - Qi Ming
./. 05 c.427C>G - p.Arg143Gly blood - GenBank MYH7_00080 - Asymmetrical septal hypertrophy. - Qi Ming
./. 05 c.427C>T - p.Arg143Trp blood - GenBank MYH7_00174 - - - Qi Ming
./. 05 c.428G>A - p.Arg143Gln blood - GenBank MYH7_00118 - - - Qi Ming
./. 05 c.428G>A - p.Arg143Gln blood - GenBank MYH7_00118 - - - Qi Ming
./. 05 c.438G>C - p.Lys146Asn blood - GenBank MYH7_00143 - Familial. - Qi Ming
./. 05 c.438G>T - p.Lys146Asn blood - GenBank MYH7_00239 - - - Qi Ming
./. 05 c.443G>C - p.Ser148Ile blood - GenBank MYH7_00081 - Asymmetrical septal hypertrophy. - Qi Ming
./. 05 c.480C>T - p.Asn160Asn blood - GenBank MYH7_00182 - Rare variant. - Qi Ming
./. 05 c.502+18G>A - - blood - GenBank MYH7_00183 - Rare variant. - Qi Ming
./. 07 c.556G>C - p.Val186Leu blood - GenBank MYH7_00144 - Familial - Qi Ming
./. 07 c.569G>C - p.Arg190Thr blood - GenBank MYH7_00027 - - - Qi Ming
./. 07 c.586G>A - p.Ala196Thr blood - GenBank MYH7_00129 - Active site. - Qi Ming
./. 07 c.597A>G - p.Ala199Ala lymphocyte - GenBank MYH7_00016 0.033 rs2069541 - Qi Ming
./. 07 c.597A>G - p.Ala199Ala blood - GenBank MYH7_00016 5/328 - - Qi Ming
./. 07 c.597A>G - p.Ala199Ala blood - GenBank MYH7_00016 - - - Qi Ming
./. 07 c.597A>G - p.Ala199Ala blood - GenBank MYH7_00016 - - - Qi Ming
./. 07 c.597A>G - p.Ala199Ala blood - GenBank MYH7_00016 - Rare variant. - Qi Ming
./. 07 c.597A>G - p.Ala199Ala Peripheral blood - GenBank MYH7_00016 - - - Qi Ming
./. 07 c.598delG - p.Ala200ProfsX64 unknown - GenBank MYH7_00350 NA - - Qi Ming
./. 07 c.602T>C - p.Ile201Thr blood - GenBank MYH7_00095 - - - Qi Ming
./. 07 c.619A>C - p.Lys207Gln blood - GenBank MYH7_00091 - atrial fibrillation, heterozygotes bradycardic. - Qi Ming
./. 07 c.632C>T - p.Pro211Leu blood - GenBank MYH7_00090 - Asymmetrical septal hypertrophy. - Qi Ming
./. 07 c.632C>T - p.Pro211Leu blood - GenBank MYH7_00090 - Active site. - Qi Ming
./. 07 c.632C>T - p.Pro 211 Leu DNA sample - GenBank MYH7_00090 - Benign - Qi Ming
./. 08 c.641G>A - p.Gly214Asp blood - GenBank MYH7_00134 - - - Qi Ming
./. 08 c.646C>G - p.Leu216Val blood - GenBank MYH7_00135 - - - Qi Ming
./. 08 c.679C>G - p.Leu227Val blood - GenBank MYH7_00107 - - - Qi Ming
./. 08 c.695A>G - p.Asn232Ser blood - GenBank MYH7_00045 - RLC binding domain and ATP binding domain. - Qi Ming
./. 08 c.695A>G - p.Asn232Ser Blood - GenBank MYH7_00045 - This mutation did not create or destroy any restriction enzyme site. - Qi Ming
./. 08 c.697G>T - p.Ala233Ser Peripheral blood - GenBank MYH7_00271 - - - Qi Ming
./. 08 c.709C>T - p.Arg237Trp unknown - GenBank MYH7_00338 NA - - Qi Ming
./. 08 c.724T>C - p.Ser242Pro unknown - GenBank MYH7_00337 NA - - Qi Ming
./. 08 c.728G>A - p.Arg243His blood - GenBank MYH7_00237 - A novel mutation (Arg243His) found in proband GB was absent from all family members. A Glu497Asp mutation produced apical HCM in proband HZ with associated ECG abnormalities of LVH and deeply inverted precordial T waves. - Qi Ming
./. 08 c.732C>T - p.Phe244Phe lymphocyte - GenBank MYH7_00017 0.267 rs2069542 - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00029 - - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00037 6/328 - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00017 - - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00017 - - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00017 - - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe blood - GenBank MYH7_00017 - - - Qi Ming
./. 08 c.732C>T - p.Phe244Phe Peripheral blood - GenBank MYH7_00017 - - - Qi Ming
./. 09 c.739T>C - p.Phe247Leu blood - GenBank MYH7_00257 - - - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - - - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - Active site. - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - LOD score: 4.0 - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - Cytochrome C oxidase activity and histoenzymatic staining were severely decreased. - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - Concentric hypertrophy. ST depression. - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood - GenBank MYH7_00046 - - - Qi Ming
./. 09 c.746G>A - p.Arg249Gln blood lymphocytes - GenBank MYH7_00046 - - - Qi Ming
./. 09 c.767G>A - p.Gly256Glu blood - GenBank MYH7_00191 - - - Qi Ming
./. 09 c.776C>A - p.Ala259Glu blood - GenBank MYH7_00136 - - - Qi Ming
./. 09 c.788T>C - p.Ile263Thr blood - GenBank MYH7_00047 - - - Qi Ming
./. 09 c.788T>C - p.Ile263Thr blood - GenBank MYH7_00047 - One sudden death at 29 years of age was reported in the family history. - Qi Ming
./. 09 c.789A>G - p.Ile263Met blood - GenBank MYH7_00149 - - - Qi Ming
./. 10 c.842G>C - p.Arg281Thr blood - GenBank MYH7_00137 - - - Qi Ming
./. 10 c.842G>C - p.Arg281Thr blood - GenBank MYH7_00137 - The mutation affects a highly conserved amino acid in the myosin subfragment-1. - Qi Ming
./. 10 c.877delA - p.Lys294SerfsX9 unknown - GenBank MYH7_00336 NA - - Qi Ming
./. 11 c.902T>A - p.Leu301Gln blood - GenBank MYH7_00247 - p.Leu301Gln is in the functionally important globular head region of b-myosin heavy chain, a region in which multiple pathogenic mutations have been described - Qi Ming
./. 11 c.926A>T - p.Asp309Val blood - GenBank MYH7_00031 - - - Qi Ming
./. 11 c.935T>G - p.Phe312Cys blood - GenBank MYH7_00150 - - - Qi Ming
./. 11 c.958G>A - p.Val320Met lymphocyte - GenBank MYH7_00013 - - - Qi Ming
./. 11 c.975C>T - p.Asp325Asp lymphocyte - GenBank MYH7_00018 0.050 rs2231124 - Qi Ming
./. 11 c.975C>T - p.Asp325Asp blood - GenBank MYH7_00018 0.96 in patient - - Qi Ming
./. 11 c.975C>T - p.Asp325Asp blood - GenBank MYH7_00018 - - - Qi Ming
./. 11 c.975C>T - p.Asp325Asp blood - GenBank MYH7_00018 - - - Qi Ming
./. 11 c.975C>T - p.Asp325Asp blood - GenBank MYH7_00018 - Rare variant. - Qi Ming
./. 11 c.975C>T - p.Asp325Asp Peripheral blood - GenBank MYH7_00018 - - - Qi Ming
./. 11 c.983A>G - p.Glu328Gly blood - GenBank MYH7_00108 - - - Qi Ming
./. 12 c.1046T>C - p.Met349Thr blood - GenBank MYH7_00151 - - - Qi Ming
./. 12 c.1046T>C - p.Met349Thr blood - GenBank MYH7_00151 - - - Qi Ming
./. 12 c.1046T>C - p.Met349Thr blood lymphocytes - GenBank MYH7_00151 - - - Qi Ming
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