Variant #0000850762 (NC_000005.9:g.131647910C>T, NM_003060.3:c.-57755C>T (SLC22A5))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.131647910C>T |
DNA change (hg38) |
- |
Published as |
SLC22A4(NM_003059.3):c.450C>T (p.F150=) |
ISCN |
- |
DB-ID |
SLC22A4_000009 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|