Variant #0000011512 (NC_000012.11:-, MYL2(NM_000432.3):c.283C>G)
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_00007 See all 2 reported entries |
Frequency |
- |
Variant remarks |
Associated with a particular subtype of cardiac hypertrophy defined by mid-left ventricular obstruction; decreased the Ca2+ binding affinity 3-fold compared with HCRLC-WT. P95A mutant also had an increase in alpha-helical content upon Ca2+ binding. |
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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