Variant #0000011516 (NC_000012.11:-, MYL2(NM_000432.3):c.64G>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_00006 See all 3 reported entries |
| Frequency |
- |
| Variant remarks |
This base change caused a loss of one of two normal Taq I restriction sites in the exon 2 amplimer allowing its independent confirmation by restriction enzyme digestion. |
| 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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