Variant #0000011511 (NC_000012.11:-, MYL2(NM_000432.3):c.173G>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_00002 See all 5 reported entries |
| Frequency |
- |
| Variant remarks |
Associated with a typical form of hypertrophic cardiomyopathy, which causes increased left ventricular wall thickness and abnormal electrocardiograph findings with no mid-cavity obliteration. Ca2+ binding to the R58Q mutant was restored upon phosphorylation. The R58Q mutation completely impaired Ca2+ binding (did not bind Ca2+ in the nonphosphorylated state but did bind Ca2+ when phosphorylated)
The R58Q mutant did not bind Ca2+ in its nonphosphorylated form, and Ca2+ did not significantly affect its alpha-helical content. However, the phosphorylation restored its Ca2+ binding and the amount of alpha-helical content greatly increased on binding of Ca2+ to phosphorylated R58Q. |
| 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
|
|