Variant #0000016542 (NC_000001.10:g.76199281delG, ACADM(NM_000016.4):c.355delG)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Type |
Deletion |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.76199281delG |
| Reference |
Shuting Wang et al. (2020) |
| DB-ID |
ACADM_000009 |
| Frequency |
1/130 |
| 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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