Variant #0000178497 (NC_000002.11:g.211471621T>A, NM_001122633.2:c.2166T>A (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.211471621T>A
DNA change (hg38) g.210606897T>A
Published as 2148T>A (N716K)
ISCN -
DB-ID CPS1_000140 See all 6 reported entries
Variant remarks corresponding variants in E.coli CPS (N301H) virtually abolish carbamoyl phosphate synthesis
Reference PubMed: Yefimenko 2004
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 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 +/. 19 c.2166T>A r.(?) p.(Asn722Lys)


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