Variant #0000016178 (NC_000005.9:g.131721164C>T, SLC22A5(NM_003060.3):c.797C>T)
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.131721164C>T |
Reference |
Weihua Lin et al.(2021) |
DB-ID |
SLC22A5_000052 |
Frequency |
14/667 |
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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