Variant #0000016256 (NC_000001.10:g.76226843A>G, ACADM(NM_000016.4):c.982A>G)
| 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.76226843A>G |
| Reference |
Tong F et al. (2019) |
| DB-ID |
ACADM_000043 |
| Frequency |
2/130 |
| 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
|
|