Variant #0000675264 (NC_000022.10:g.19165709C>T, NM_005984.3:c.139G>A (SLC25A1))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.19165709C>T |
| DNA change (hg38) |
g.19178196C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC25A1_000029 |
| Variant remarks |
overexpression in deficient fibroblasts showed severely impaired CIC activity (below 25%) |
| Reference |
PubMed: Pop 2018, Journal: Pop 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Eric Wever |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-08-05 14:33:49 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|