Variant #0000016632 (NC_000004.11:g.159620140_159624743del, ETFDH(NM_004453.2):c.974_1285del)
Chromosome |
4 |
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.159620140_159624743del |
Reference |
- |
DB-ID |
ETFDH_000075 |
Frequency |
1/671 |
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
|
|