Variant #0000578192 (NC_000017.10:g.42078968C>A, NAGS(NM_153006.2):c.-3064C>A)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.42078968C>A
DNA change (hg38) g.44001600C>A
Published as c.-3064C>A
ISCN -
DB-ID NAGS_000019
Variant remarks functional assays demonstrate that this variant decreases both transcription and binding of HNF-1, a known NAGS transcription factor, to the NAGS gene; not in 1086 controls
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nicholas Ah Mew
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAGS NM_153006.2 +/. 1 c.-3064C>A r.(=) p.(=)