Variant #0000011521 (NC_000012.11:-, MYL2(NM_000432.3):c.37G>A)
Chromosome |
12 |
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 |
MYL2_00003 See all 4 reported entries |
Frequency |
- |
Variant remarks |
The present results suggest that either the MYL2 mutation or the MYH7 mutation alone may cause HCM respectively, but the presence of both MYL2 and the MYH7 mutation may result in a more severe disease than either mutation alone as seen in the case of the proband. |
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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