Variant #0000016258 (NC_000001.10:g.76226901G>T, ACADM(NM_000016.4):c.1040G>T)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.76226901G>T |
| Reference |
Zhuwen Gong et al. (2021) |
| DB-ID |
ACADM_000046 |
| Frequency |
5/130 |
| 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
|
|