Variant #0000987526 (NC_000009.11:g.133342160C>T, NM_000050.4:c.469C>T (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.133342160C>T
DNA change (hg38) g.130466773C>T
Published as R157C
ISCN -
DB-ID ASS1_000084 See all 8 reported entries
Variant remarks cDNA expression cloning shows no 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) 2.0E-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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASS1 NM_000050.4 +/. - c.469C>T - p.Arg157Cys


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