Variant #0000016547 (NC_000012.11:g.121176670_121176672del, ACADS(NM_000017.2):c.981_983del)
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Type |
Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121176670_121176672del |
| Reference |
Shuting Wang et al. (2020) |
| DB-ID |
ACADS_000024 |
| Frequency |
1/179 |
| Variant remarks |
- |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
ting zhang |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
ting zhang |

Variant on transcripts
|
|