Variant #0000016149 (NC_000005.9:g.131706062G>A, SLC22A5(NM_003060.3):c.393+5G>A)
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.131706062G>A |
Reference |
Han L et al. (2014) |
DB-ID |
SLC22A5_000023 |
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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