Variant #0000016397 (NC_000001.10:g.53676453C>G, CPT2(NM_000098.2):c.1107C>G)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53676453C>G |
Reference |
- |
DB-ID |
CPT2_000009 |
Frequency |
1/28 |
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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