Variant #0000987514 (NC_000009.11:g.133333884A>C, NM_000050.4:c.271A>C (ASS1))

Chromosome 9
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.133333884A>C
DNA change (hg38) g.130458497A>C
Published as T91P
ISCN -
DB-ID ASS1_000127 See all 4 reported entries
Variant remarks cDNA expression cloning shows <0.05 argininosuccinate synthetase enzyme activity
Reference PubMed: Diez-Fernandez 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-06-03 16:23:50 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASS1 NM_000050.4 +/. - c.271A>C - p.Thr91Pro


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