Variant #0000016367 (NC_000011.9:g.68566802del, CPT1A(NM_001876.3):c.577delC)
| Chromosome |
11 |
| 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.68566802del |
| Reference |
- |
| DB-ID |
CPT1A_000006 |
| Frequency |
2/53 |
| 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
|
|