Variant #0000016616 (NC_000004.11:g.159624745T>C, ETFDH(NM_004453.2):c.1285+2T>C)
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.159624745T>C |
Reference |
- |
DB-ID |
ETFDH_000099 |
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
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