Variant #0000011314 (NC_000014.8:-, MYH7(NM_000257.2):c.?)

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type blood
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYH7_00238
Frequency -
Variant remarks the Glu497Asp mutation caused massive

concentric hypertrophy (interventricular septum29 mm);

after a syncopal episode, an automatic implanted cardioverter/

defibrillator was implanted in this patient
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 ./. 15 c.? - p.Glu497Asp