Variant #0000016191 (NC_000005.9:g.131726450T>C, SLC22A5(NM_003060.3):c.1121T>C)
| 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.131726450T>C |
| Reference |
Xiaole li et al.(2019) |
| DB-ID |
SLC22A5_000070 |
| Frequency |
1/667 |
| 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
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