Variant #0000849668 (NC_000002.11:g.211454831G>A, NM_001122633.2:c.731G>A (CPS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.211454831G>A
DNA change (hg38) -
Published as CPS1(NM_001875.4):c.713G>A (p.R238Q), CPS1(NM_001875.5):c.713G>A (p.(Arg238Gln))
ISCN -
DB-ID CPS1_000310 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) 0.00034 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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.731G>A r.(?) p.(Arg244Gln)
CPS1 NM_001875.4 ?/. - c.713G>A r.(?) p.(Arg238Gln)


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