Variant #0000016212 (NC_000005.9:g.131728268C>T, SLC22A5(NM_003060.3):c.1411C>T)
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.131728268C>T |
| Reference |
Ni-Chung Lee et al.(2009) |
| DB-ID |
SLC22A5_000094 |
| Frequency |
2/667 |
| 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
|
|