Variant #0001068919 (NC_000023.10:g.38211835C>T, NM_000531.5:c.-115C>T (OTC))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.38211835C>T |
| DNA change (hg38) |
g.38352582C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
OTC_000454 See all 2 reported entries |
| Variant remarks |
in vitro expression analysis shows reduced reporter gene expression (0.45 in HuH-7 cells); reduced binding HNF4 transcription factor |
| Reference |
PubMed: Yang 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2026-03-02 16:39:58 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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