Variant #0000011509 (NC_000012.11:-, MYL2(NM_000432.3):c.54C>A)
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
BL21 expression host cells; Sf9 cells |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
MYL2_00005 See all 2 reported entries |
| Frequency |
- |
| Variant remarks |
(The article doesn't mention if it's c.54C>A or c.54C>G.)
Associated with a typical form of hypertrophic cardiomyopathy, which causes increased left ventricular wall thickness and abnormal electrocardiograph find- ings with no mid-cavity obliteration; decreased the Ca2+ binding affinity ~3-fold compared with HCRLC-WT. No effect of phosphorylation on Ca2+ binding to F18L was observed. |
| 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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