Variant #0000011519 (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 |
Blood |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MYL2_00002 See all 5 reported entries |
Frequency |
- |
Variant remarks |
MYL2 mutations are predicted to alter the phosphorylation site and the Ca2+ binding properties. Distribution of the disease genes of the full 197 case series was as follows: MYBPC3, 26%; MYH7, 25%; TNNT2, 4%; TNNI3, 4%; MYL2, 2.5%; and MYL<0.5%. |
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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