Variant #0000354928 (NC_000005.9:g.81572002A>T, NM_001025.4:c.358T>A (RPS23))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Probably does not affect function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.81572002A>T |
| DNA change (hg38) |
g.82276183A>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RPS23_000002 See all 3 reported entries |
| Variant remarks |
expression cloning in yeast (confirmed) and E. coli (confirmed) indicate the variant does not influence function |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marc Pieterse |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-02-22 14:24:05 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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