Variant #0000016282 (NC_000012.11:g.121176355G>A, ACADS(NM_000017.2):c.815G>A)
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121176355G>A |
Reference |
- |
DB-ID |
ACADS_000020 |
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
|
|