Variant #0000514097 (NC_000002.11:g.211473070G>T, NC_000002.11(NM_001122633.2):c.2211-15G>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.211473070G>T
DNA change (hg38) g.210608346G>T
Published as CPS1(NM_001122633.2):c.2211-15G>T, CPS1(NM_001875.5):c.2193-15G>T
ISCN -
DB-ID CPS1_000007 See all 4 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) 0.12622 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.2211-15G>T r.(=) p.(=)
CPS1 NM_001875.4 -/. - c.2193-15G>T r.(=) p.(=)


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