Variant #0000514099 (NC_000002.11:g.211476897C>T, NM_001122633.2:c.2466C>T (CPS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.211476897C>T
DNA change (hg38) g.210612173C>T
Published as CPS1(NM_001122633.2):c.2466C>T (p.C822=), CPS1(NM_001122633.3):c.2448C>T (p.C816=), CPS1(NM_001875.5):c.2448C>T (p.C816=)
ISCN -
DB-ID CPS1_000009 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01877 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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 -/. - c.2466C>T r.(?) p.(Cys822=)
CPS1 NM_001875.4 -/. - c.2448C>T r.(?) p.(Cys816=)


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