Variant #0000011505 (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 |
human cosmid |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MYL2_00003 See all 4 reported entries |
Frequency |
- |
Variant remarks |
The amino acid that is mutated, as well as the flanking sequence, shows strong evolutionary conservation. The individual with the Ala13Thr mutation was strikingly similar to that seen in patients with ELC mutations in that is showed the pronounced mid cavity obstruction. |
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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