Variant #0000566856 (NC_000019.9:g.33792747_33792752dup, NM_004364.3:c.584_589dup (CEBPA))

Chromosome 19
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.33792747_33792752dup
DNA change (hg38) g.33301841_33301846dup
Published as CEBPA(NM_001285829.1):c.227_232dup (p.(His76_Pro77dup)), CEBPA(NM_004364.5):c.584_589dupACCCGC (p.H195_P196dup)
ISCN -
DB-ID CEBPA_000019 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEBPA NM_004364.3 -/. - c.584_589dup r.(?) p.(His195_Pro196dup)


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