Variant #0000264984 (NC_000002.11:g.211342502G>A, NC_000002.11(NM_001122633.2):c.3+12G>A (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.211342502G>A
DNA change (hg38) g.210477778G>A
Published as CPS1(NM_001122633.2):c.3+12G>A, CPS1(NM_001122633.3):c.-16+12G>A
ISCN -
DB-ID CPS1_000245 See all 3 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) 0.51248 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 2018-01-15 20:58:59 +01:00 (CET)
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.3+12G>A r.(=) p.(=)
CPS1 NM_001875.4 -/. - c.-78956G>A r.(?) p.(=)
LANCL1 NM_006055.2 -/. - c.-1175C>T r.(?) p.(=)


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