Variant #0001068921 (NC_000023.10:g.38211844C>A, NM_000531.5:c.-106C>A (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.38211844C>A
DNA change (hg38) g.38352591C>A
Published as -
ISCN -
DB-ID OTC_000448 See all 15 reported entries
Variant remarks in vitro expression analysis shows reduced reporter gene expression (0.6 in HuH-7 cells); reduced binding HNF4 transcription factor
Reference PubMed: Yang 2018
ClinVar ID -
dbSNP ID rs749748052
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-03-02 16:39:58 +01:00 (CET)
Date last edited 2026-03-03 14:24:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTC NM_000531.5 +?/. 1 c.-106C>A r.(?) p.(=)


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