Variant #0000016237 (NC_000001.10:g.76205776A>G, ACADM(NM_000016.4):c.580A>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.76205776A>G |
Reference |
Tong F et al. (2019) |
DB-ID |
ACADM_000021 |
Frequency |
8/130 |
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
|
|