Variant #0000016234 (NC_000001.10:g.76200537_76200540del, ACADM(NM_000016.4):c.449_452del)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Type |
Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.76200537_76200540del |
| Reference |
Benjing Wang et al. (2019) |
| DB-ID |
ACADM_000015 |
| Frequency |
32/130 |
| 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
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