Variant #0000514088 (NC_000002.11:g.211444452T>C, NM_001122633.2:c.504T>C (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.211444452T>C
DNA change (hg38) g.210579728T>C
Published as CPS1(NM_001875.4):c.486T>C (p.Y162=), CPS1(NM_001875.5):c.486T>C (p.Y162=)
ISCN -
DB-ID CPS1_000271 See all 2 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) 0.00339 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.504T>C r.(?) p.(Tyr168=)
CPS1 NM_001875.4 -/. - c.486T>C r.(?) p.(Tyr162=)


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