Variant #0000011506 (NC_000012.11:-, MYL2(NM_000432.3):c.52T>C)
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Human cosmid |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MYL2_00001 See all 2 reported entries |
Frequency |
- |
Variant remarks |
Detected from the mutations in the regulatory light chain.
The amino acids that are mutated, as well as he flanking sequence, show strong evolutionary conservation. The cardiac morphology in three patients from two unrelated families with the Glu22Lys mutation was strikingly similar to that seen in patients with ELC mutation. |
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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