Variant #0000011313 (NC_000014.8:-, MYH7(NM_000257.2):c.728G>A)
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_00237 |
Frequency |
- |
Variant remarks |
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. |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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