Variant #0000011515 (NC_000012.11:-, MYL2(NM_000432.3):c.132T>C)
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_00012 |
Frequency |
- |
Variant remarks |
Five more frequent SNPs were located in the exon flanking regions of introns 4 and 5 of MYL2 (three nucleotide substitutions, one insertion and one deletion). |
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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