Variant #0000178749 (NC_000002.11:g.211456617A>G, NM_001122633.2:c.1028A>G (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.211456617A>G
DNA change (hg38) g.210591893A>G
Published as 1010A>G His337Arg)
ISCN -
DB-ID CPS1_000026 See all 2 reported entries
Variant remarks CPSI expression studies show 70% 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPS1 NM_001122633.2 +/. 11 c.1028A>G r.(?) p.(His343Arg)


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