Variant #0000178610 (NC_000002.11:g.211441201C>T, NM_001122633.2:c.386C>T (CPS1))

Chromosome 2
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.211441201C>T
DNA change (hg38) g.210576477C>T
Published as 368C>T (S123F)
ISCN -
DB-ID CPS1_000061 See all 2 reported entries
Variant remarks CPSI expression studies show 60% decreased activity
Reference PubMed: Pekkala 2010
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-10-08 00:34:47 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPS1 NM_001122633.2 +/. 4 c.386C>T r.(?) p.(Ser129Phe)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.