Variant #0001034707 (NC_000004.11:g.8594571dup, NM_003652.3:c.11dup (CPZ))

Chromosome 4
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.8594571dup
DNA change (hg38) -
Published as CPZ(NM_001014447.3):c.11dup (p.(Leu5Alafs*21))
ISCN -
DB-ID CPZ_000011
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPZ NM_003652.3 ?/. - c.11dup r.(?) p.(Leu5Alafs*21)
GPR78 NM_080819.4 ?/. - c.*5481dup r.(?) p.(=)


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