Variant #0000016362 (NC_000011.9:g.68582817_68582819del, CPT1A(NM_001876.3):c.124_126delAAG)
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.68582817_68582819del |
Reference |
- |
DB-ID |
CPT1A_000001 |
Frequency |
1/53 |
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
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