Variant #0000980226 (NC_000012.11:g.31247557dup, NM_030653.3:c.1403dup (DDX11))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31247557dup
DNA change (hg38) -
Published as DDX11(NM_030653.3):c.1403dupT (p.S469Vfs*32), DDX11(NM_030653.4):c.1403dup (p.(Ser469ValfsTer32))
ISCN -
DB-ID DDX11_000005 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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX11 NM_030653.3 +/. - c.1403dup r.(?) p.(Ser469Valfs*32)


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