Variant #0000270569 (NC_000002.11:g.211527838_211527839del, NC_000002.11(NM_001122633.2):c.3946-9_3946-8del (CPS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.211527838_211527839del
DNA change (hg38) g.210663114_210663115del
Published as CPS1(NM_001122633.3):c.3928-9_3928-8delTT, CPS1(NM_001875.5):c.3928-9_3928-8delTT
ISCN -
DB-ID CPS1_000262 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.3946-9_3946-8del r.(=) p.(=)
CPS1 NM_001875.4 -?/. - c.3928-9_3928-8del r.(=) p.(=)


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