Variant #0000016453 (NC_000004.11:g.159618751T>G, ETFDH(NM_004453.2):c.872T>G)
| Chromosome |
4 |
| 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.159618751T>G |
| Reference |
- |
| DB-ID |
ETFDH_000069 |
| Frequency |
7/671 |
| 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
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