Variant #0000016391 (NC_000001.10:g.53676232C>T, CPT2(NM_000098.2):c.886C>T)
| Chromosome |
1 |
| 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.53676232C>T |
| Reference |
- |
| DB-ID |
CPT2_000003 |
| 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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